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Transcriber’s Note

Changes to the text are limited to typographical errors,
as listed at the end of the book.

Note that numerous taxonomic names have changed since 1894. The
formatting of Latin names also differs from current conventions; e.g., in
this book species names are typically, but not invariably, capitalised.
No attempt has been made to update this.

The woodcut illustrations of adult insects from Figure 65 onwards have
been prepared with thumbnails which preserve the same scale as the
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BUTTERFLIES AND MOTHS
(BRITISH)

OUT-DOOR WORLD LIBRARY.


THE OUT-DOOR WORLD; or, Young Collector’s
Handbook. By W. Furneaux, F.R.G.S. With 18
Plates, 16 of which are coloured, and 549 Illustrations in
the Text. Crown 8vo. 7s. 6d.

BUTTERFLIES AND MOTHS (British).
By W. Furneaux, F.R.G.S. With 12 coloured Plates and
241 Illustrations in the Text. 10s. 6d. net.

To be followed by

BRITISH BIRDS. By W. H. Hudson, F.Z.S.
With a Chapter on Structure and Classification by Frank
E. Beddard
, F.R.S.

LIFE IN PONDS AND STREAMS. By
W. Furneaux, F.R.G.S.

BRITISH MAMMALS AND REPTILES.
AND OTHER VOLUMES.


London: LONGMANS, GREEN, & CO.
New York: 15 East 16th Street.



Plate I

Danielsson & Co., del. ad. Nat. et Chromolith.


BUTTERFLIES AND MOTHS
(BRITISH)

BY

W. FURNEAUX, F.R.G.S.

AUTHOR OF ‘THE OUT-DOOR WORLD, OR YOUNG COLLECTOR’S HANDBOOK’

WITH TWELVE COLOURED PLATES
AND NUMEROUS ILLUSTRATIONS IN THE TEXT

 

 

 

LONDON

LONGMANS, GREEN, AND CO.
AND NEW YORK. 15 EAST 16th STREET

1894

All rights reserved


[Pg v]

PREFACE

The favourable reception with which the ‘Out-door World’
has been greeted has encouraged the publishers to issue
a series of volumes dealing in fuller detail with the various
branches of Natural History treated of in that work.
Necessarily each subject was only briefly touched upon, but
the study is of so enticing a character that ‘appetite grows
by feeding,’ and the students of the ‘Out-door World,’
having tasted the sweetness of companionship with Nature,
will not rest satisfied with the help afforded by that handbook.
Each one will want to go deeper into that particular department
which most appeals to his own inclinations.

The present volume is written expressly for those who
desire to extend their knowledge of the British Lepidoptera,
or, to use the more popular names, ‘Butterflies and Moths.’

The general characteristics of this interesting order of
insects are described somewhat fully, but, of course, it would
be impossible to give an individual account of all the British
Lepidoptera in a work of this size, so a selection has been
made such as will satisfy the requirements of the great majority
of those who intend to take up this particular branch[Pg vi]
of entomology. The number of British Butterflies, however, is
so limited that a place has been found for a figure and a description
of every species; and, of the larger moths, many
of the common and typical kinds have been included. An
introduction to the study of the Micro-lepidoptera has also
been added.

No trouble has been spared to render this work thoroughly
practical. In addition to the verbal descriptions of so many
species, twelve coloured plates and a large number of woodcuts
have been specially prepared to help the student in his
work. It is believed that the extreme care with which these
have been produced will render them of the greatest assistance
to the collector in the recognition of his specimens.

But he has not only to recognise his specimens—he must
first catch them; and here full directions have been given to
insure success in this part of his work, as well as in the
management, preservation, and arrangement of his captures.

The Author hopes that this volume may be the means of
adding many happy hours—hours of the purest enjoyment—to
the lives of those whom he has succeeded in luring into
the fields and lanes and woods of the Out-door World.

[Pg vii]

CONTENTS

PART I
STRUCTURE AND LIFE HISTORY OF THE LEPIDOPTERA
CHAP. PAGE
I.GENERAL CHARACTERS1
II.THE EGG16
III.THE LARVA22
IV.THE PUPA OR CHRYSALIS44
V.CLASSIFICATION OF THE LEPIDOPTERA55
PART II
WORK AT HOME AND IN THE FIELD
VI.CATCHING BUTTERFLIES AND MOTHS63
VII.COLLECTING OVA, LARVÆ, AND PUPÆ98
VIII.REARING LEPIDOPTERA112
IX.SETTING AND PRESERVING122
X.PRESERVING OVA, LARVÆ AND PUPÆ130
XI.THE CABINET—ARRANGEMENT OF SPECIMENS134
PART III
BRITISH BUTTERFLIES
XII.THE SWALLOW-TAIL AND THE ‘WHITES’139
XIII.THE FRITILLARIES, VANESSAS, AND THE PURPLE EMPEROR154
XIV.THE BROWNS AND HEATHS173
XV.THE HAIRSTREAKS, COPPERS AND BLUES183[Pg viii]
XVI.THE DUKE OF BURGUNDY AND THE SKIPPERS196
PART IV
COMMON BRITISH MOTHS
XVII.SPHINGES203
XVIII.BOMBYCES217
XIX.THE NOCTUÆ239
XX.GEOMETRÆ268
XXI.THE MICRO-LEPIDOPTERA290
APPENDICES
I.COMPLETE CLASSIFIED LIST OF BRITISH MACRO-LEPIDOPTERA309
II.THE LEPIDOPTERIST’S CALENDAR326
References To Coloured Plates347
Index351

[Pg ix]

LIST OF ILLUSTRATIONS

COLOURED PLATES

1-7.British ButterfliesFrontispiece
8.Larvæ and Pupæ of British Butterflies}At end
9.Sphinges
10.Bombyces
11.Noctuæ
12.Noctua and Geometræ

Full references accompany the Plates.

ILLUSTRATIONS IN THE TEXT

FIG. PAGE
1.Scales from the Wings of Butterflies1
2.Portion of the Wing of a Butterfly from which some of the Scales have been removed2
3.Body of a Butterfly—Under Side3
4.Section of the Eye of an Insect4
5.Antennæ of Butterflies5
6.Antennæ of Moths5
7.Section of the Proboscis of a Butterfly7
8.Diagram of the Wings of a Butterfly9
9.The Undeveloped Fore Leg of a Butterfly10
10.The Four Stages of the Large White Butterfly (Pieris Brassicæ)14
11.Egg of the Meadow Brown Butterfly20
12.Egg of the Speckled Wood Butterfly20
13.Egg of the Vapourer Moth20
14.The Caterpillar of the Clouded Yellow Butterfly22
15.The Caterpillar of the Dark Green Fritillary Butterfly23
16.The Caterpillar of the Purple Emperor Butterfly24[Pg x]
17.An Ichneumon Fly (Cryptus Migrator)25
18.Another Ichneumon Fly (Pimpla Instigator)25
19.The Caterpillar of the Angle Shades Moth (Meticulosa)26
20.Walking Leg of a Caterpillar28
21.Larva of the Yellow Underwing Moth (Pronuba)28
22.Larva of the Crimson Speckled Moth (Pulchella)28
23.Larva of the Lobster Moth (Fagi)28
24.Caterpillar of the Iron Prominent Moth (Dromedarius)29
25.Larva of the Brimstone Moth (Luteolata)29
26.The Claspers of a Caterpillar30
27.The Homes of Leaf Miners and Leaf Rollers33
28.The Cocoon of the Emperor Moth40
29.The Cocoon of the Six-Spotted Burnet (Filipendulæ)40
30.The Pupa of the Privet Hawk (Ligustri)44
31.The Chrysalis of the Large White Butterfly (Brassicæ)44
32.The Pupa of the Dark Green Fritillary (Aglaia)45
33.The Pupa of the Black-veined White Butterfly (Cratægi)45
34.The Pupa of the Currant Moth45
35.Pupa of the Pale Tussock Moth (Pudibunda)45
36.A Butterfly, just after Emerging50
37.A Butterfly at Rest (Large Copper)57
38.A Moth at Rest (Gothic)57
39.A Wire Frame for a Butterfly Net65
40.Stick for the Net65
41.The Metal Y66
42.Pattern for the Net67
43.The Cyanide Bottle68
44.Section of the Laurel Box70
45.The Chloroform Bottle72
46.} Fittings for the Collecting Box75
47.
48.
49.
50.Frame of Net for Collecting Insects on Lamps and Windows87
51.A Trap for Catching Moths88
52.Metal Joint for Lantern and Net91
53.Net and Lantern for Taking Moths from High Blossoms91
54.Frame for the Sugaring Net94
55.Cage for Decoy Females96
56.A Sugar Trap96
57.A Larva Glass114
58.A Larva Glass114
59.A Larva Cage115
60.Section of a Setting Board123
61.Sections of Setting Boards123
62.A Butterfly on the Setting Board124[Pg xi]
63.Another Method of Setting Butterflies and Moths126
64.A Blowpipe for Larvæ131
65.The Bath White—Under Side147
66.The Clouded Yellow—Female151
67.The Small Pearl-bordered Fritillary—Under Side155
68.The Pearl-bordered Fritillary—Under Side156
69.The Queen of Spain Fritillary—Under Side157
70.The Dark-green Fritillary—Under Side158
71.The High-brown Fritillary159
72.The Silver-washed Fritillary—Under Side160
73.The Greasy Fritillary—Under Side161
74.The Glanville Fritillary—Under Side162
75.The Comma—Under Side164
76.The Purple Emperor—Under Side172
77.The Marbled White—Under Side174
78.The Wood Argus—Under Side176
79.The Grayling—Under Side178
80.The Large Heath—Under Side179
81.The Ringlet—Upper Side180
82.The Marsh Ringlet—Under Side181
83.The Brown Hairstreak—Male184
84.The White-letter Hairstreak184
85.The Purple Hairstreak—Male186
86.The Green Hairstreak186
87.The Tailed Blue—Under Side188
88.The Silver-studded Blue—Under Side189
89.The Common Blue—Under Side191
90.The Clifden Blue—Under Side191
91.The Chalk-hill Blue—Under Side192
92.The Holly Blue—Under Side193
93.The Mazarine Blue—Under Side194
94.The Small Blue—Under Side194
95.The Large Blue—Under Side195
96.The Silver-spotted Skipper—Under Side201
97.The Death’s-head Hawk Moth205
98.The Larva of Atropos206
99.The Caterpillar of Euphorbiæ207
100.The Small Elephant Hawk Moth208
101.The Poplar Hawk209
102.The Broad-bordered Bee Hawk212
103.The Hornet Clearwing of the Poplar213
104.The Currant Clearwing213
105.The Forester214
106.The Six-spotted Burnet215
107.The Larva of Filipendulæ215
108.The Green Silver-lined217
109.The Short-cloaked Moth218[Pg xii]
110.The Muslin Moth218
111.The Common Footman219
112.The Larva of Jacobææ219
113.The Scarlet Tiger220
114.The Buff Ermine222
115.The White Ermine222
116.The Ghost Swift—Female223
117.The Common Swift224
118.The Goat Moth225
119.The Larva of Ligniperda (less than half full size)225
120.The Leopard Moth226
121.The Larva of Pyrina (only partly grown)226
122.The Brown Tail227
123.The Gipsy—Male227
124.The Black Arches—Male228
125.The Vapourer Moth—Male228
126.The Female Vapourer228
127.Larva of the Vapourer Moth229
128.The Drinker—Male230
129.The Oak Hook Tip233
130.The Chinese Character233
131.The Poplar Kitten234
132.The Puss Moth235
133.The Coxcomb Prominent235
134.The Larva of Bucephala236
135.The Chocolate Tip237
136.The Peach Blossom237
137.The Yellow Horned238
138.The Marbled Beauty240
139.The Grey Dagger240
140.The Poplar Grey241
141.The Figure of Eight241
142.The Brown-line Bright-eye242
143.The Smoky Wainscot243
144.The Common Wainscot243
145.The Bullrush244
146.The Frosted Orange245
147.The Flame245
148.The Light Arches246
149.The Flounced Rustic246
150.The Cabbage Moth247
151.The Dot247
152.The Rustic Shoulder-knot248
153.The Marbled Minor248
154.The Mottled Rustic249
155.The Turnip Moth250
156.The Heart and Dart251[Pg xiii]
157.The Garden Dart251
158.The Flame Shoulder252
159.The Lesser Broad Border252
160.The Lesser Yellow Underwing253
161.The Gothic254
162.The Old Lady254
163.The Common Quaker255
164.The Chestnut256
165.The Pink-barred Sallow256
166.The Dun-bar257
167.The Broad-barred White257
168.The Angle Shades258
169.The Grey Arches259
170.The Shears260
171.The Bright-line Brown-eye260
172.The Early Grey261
173.The Shark262
174.The Burnished Brass263
175.The Silver Y264
176.The Red Underwing266
177.The Light Emerald270
178.The August Thorn271
179.The Peppered Moth272
180.The Willow Beauty273
181.The Large Emerald274
182.The Common Emerald274
183.The Lace Border275
184.The Riband Wave276
185.The Blood-vein276
186.The Common Wave277
187.The Clouded Silver277
188.The V Moth278
189.The Common Heath279
190.The Bordered White—Male279
191.The Currant Moth280
192.The Spring Usher281
193.The March Moth282
194.The November Moth282
195.The Twin-spot Carpet283
196.The Grass Rivulet283
197.The Netted Pug284
198.The Narrow-winged Pug284
199.The Brindled Pug284
200.The Small Seraphim285
201.The Blue-bordered Carpet285
202.The Beautiful Carpet286[Pg xiv]
203.The Common Carpet286
204.The Silver Ground Carpet287
205.The Garden Carpet287
206.The Yellow Shell288
207.The Small Phœnix288
208.The Small Mallow289
209.The Tabby or Grease Moth291
210.The Meal Moth292
211.The Small Magpie292
212.The Mother-of-Pearl293
213.The Garden Pebble293
214.The Beautiful China Mark294
215.Gonodactyla295
216.Osteodactylus295
217.Pentadactyla295
218.Hexadactyla—Enlarged296
219.Phragmitellus—Enlarged one-half297
220.Hamellus—Slightly Enlarged297
221.Tristellus297
222.Hortuellus298
223.Mellonella298
224.Xylosteana with wings closed299
225.Viridana300
226.Cristana—Enlarged300
227.Lecheana300
228.Pruniana300
229.Salicella301
230.Octomaculana—Enlarged301
231.Cirsiana—Enlarged302
232.Pomonella302
233.Zoegana—Enlarged302
234.Fagella303
235.Cuprella304
236.Padellus304
237.Nervosa—Twice Natural Size304
238.Geoffrella305
239.Ibipennella—Enlarged305
240.Complanella—Enlarged306
241.Aurella—Enlarged307

[Pg 1]

PART I

STRUCTURE AND LIFE-HISTORY
OF THE LEPIDOPTERA


CHAPTER I

GENERAL CHARACTERS

The word Lepidoptera, which you see at the head of this page, is
the name of the order of insects to which this volume is to be
devoted. It is formed from two Greek words, one (lepis) signifying
a scale, and the other (pteron) denoting a wing; and was
applied by the great naturalist Linnæus to the scaly-winged insects
popularly known as Butterflies
and Moths.


Fig. 1.—Scales from the Wings of
Butterflies.

Every one of my readers
has undoubtedly handled some
of the interesting creatures of
this group—having been led
to do so either by the extreme
beauty of their clothing, or,
perhaps, from a murderous
intent in order to protect his
own garments from the ravages
of a supposed marauder. A light mealy powder will probably have
been observed afterwards on the fingers that have touched the
victim’s wings.

This powder, although it sometimes presents a beautiful glossy
surface when spread over the skin, does not exhibit any definite
form or structure without a more minute examination. Yet these[Pg 2]
are the scales that led the immortal naturalist to invent the somewhat
long but useful term Lepidoptera.

The very next time the opportunity offers itself, dust off a little
of the mealy powder with a small and very soft brush on to a
strip of white paper or a slip of glass, and examine it with a
powerful lens or the low power of a compound microscope. What
a sight you will then behold! Each little particle of dust is a
beautifully formed scale, stamped with a number of minute
rounded projections, and often displaying the most gorgeous colours.
A great variety of designs and tints are often exhibited by the
‘dust’ from a single wing. Take, for instance, for your inspection,
scales from the wing of one of our commonest insects, the Small
Tortoiseshell Butterfly (Plate
III
), and you will be surprised
at the pleasing contrasts. But
when your curiosity leads you
to deal with others in the same
manner, the varied display of
forms and colours is simply
amazing.


Fig. 2.—Portion of the Wing of a
Butterfly from which some of
the scales have been removed.

In order that we may learn
still more of the structure of
the wings of the Lepidoptera,
we will examine a portion of
one from which some of the
scales have been removed,
again bringing the lens or the
microscope into our service.
We now see that the scales
are arranged in rows with great regularity on a thin and transparent
membrane, which is supported by a system of branching
rays. And the membrane itself, in parts which have been laid
bare, is marked with regular rows of dots—the points at which
the scales were originally attached by means of short hollow
rods.

The framework that supports the thin membrane we have
spoken of as consisting of a system of rays, but to these the terms
veins, nerves, nervures, or nervules are more commonly applied by
various naturalists. We cannot do better, however, than adhere
to the name originally used, for the structures in question do not
perform the functions of veins, though at first they contain blood,[Pg 3]
nor are they themselves parts of the nervous systems of the insects
to which they belong.

The result of our examination of the wings of butterflies and
moths has been to justify the application of the term Lepidoptera;
but we must now study other equally important and interesting
features of the structure of these insects. First, let us note the
general form of the body.


Fig. 3.—Body of a Butterfly—Under
Side.

1-7, segments of the abdomen;
8, anal extremity; a, antennæ;
b, tarsus; c, tibia; d, femur;
e, palpi; f, head; g, thorax.

A cursory glance at this portion of the
creature’s anatomy will show that it consists
of three distinct and well-defined
parts. In front there is the head, the size
of which is somewhat small in proportion.
Two very large eyes make up the greater
portion of its bulk. It is remarkable, too,
that butterflies possess eyes proportionately
much larger than those of moths.
Now, since butterflies always fly by day,
and moths are, generally speaking, nocturnal
insects, we might be led to suppose
that the reverse of this arrangement would
have suited the creatures better; for a
small eye, we should think, would be able
to collect sufficient light in the daytime
to form a bright image, and a larger light-receiving
area would be necessary during
the darker hours for the same purpose.
But it is evident that the sense of vision
must depend on other conditions besides
the size of the eye; and as these conditions
are not understood in relation to the
eyes of insects, any attempt at an explanation
would be quite useless.

The eye of a butterfly or moth is worthy
of a closer examination, for it is a most beautiful and marvellous
structure. The outer globular transparent membrane—the cornea—is
divided into a large number of minute polygonal facets, each
one of which admits light into a small conical compartment surrounded
by a coloured membrane, and supplied with a fibre of the
nerve of vision (the optic nerve). Hence the eye is often spoken of
as compound.

If you look closely into the eyes of various butterflies and moths[Pg 4]
you will generally see a ground colour of grey, blue, brown, or
black; but when viewed at certain angles in a strong light the
most gorgeous hues of metallic brilliancy—gold, copper, and bronze—are
to be observed. All such colours are due to the reflection of
light from the colouring matter that lies between the numerous
conical compartments.


Fig. 4.—Section of the
Eye of an Insect.

A glance at the section of a compound eye will show
you that all the little cones radiate from a common centre.
And, as each little compartment is surrounded by opaque
colouring matter, it is clear that perpendicular rays only are
capable of penetrating to its base and exciting the nerve fibre that
lies there. Thus each little division of a compound eye forms its
own image of the object that happens to be exactly opposite its
facet. But how many facets do we find in a single eye? Sometimes
only a few hundreds, but sometimes
as many as seventeen or eighteen
thousand! We must not, however,
conclude that the nature of the vision
of butterflies and moths is necessarily
very different from our own. We have
two eyes, but the images formed by them
are both blended, so that we do not see
double. We can understand, therefore,
that the thousands of images formed in
a single eye may be blended together so
as to form one continuous picture. Still
there remains this difference: while in our own case the two images
formed by the two eyes are practically the same, in the case of
insects every one of the little conical tubes of a compound eye
forms an image of an object that cannot possibly be formed by any
one of the others. Thus, if the lepidopterous insect sees a continuous
picture of its surroundings, such a picture is produced by the overlapping
and blending, at their edges, of hundreds or thousands of
distinct parts.

There is yet another interesting difference between the vision
of these insects and that of ourselves. As already stated, our two
eyes are both turned toward the same point at the same time.
But look at the butterfly’s eyes. Here are no movable eyeballs,
and the two eyes, placed as they are at the sides of the head, are
always turned in opposite directions. The corneæ, too, are very
convex; and consequently the range of vision is vastly wider than[Pg 5]
ours. A boy is often easily surprised by a playmate who approaches
him stealthily from behind, but did you ever try the same game
with a butterfly? I have, many a time. After getting cautiously
so near to a butterfly at rest as to be able to distinguish between
its head and its hinder extremity, I have quietly circled round it so
as to approach it from behind, being at the time under the impression
that it wouldn’t see me under those circumstances. But not
the slightest advantage did I derive from this stratagem, for the
position and construction of its eyes enabled it to see almost all
ways at once.

In addition to the two compound eyes, the Lepidoptera, or at
least most of them, are provided with two small simple eyes;
but these are generally so hidden among the closely set hair that
covers the head, that it is doubtful whether they are of much
service as organs of vision.


Fig. 5.—Antennæ of
Butterflies.

Fig. 6.—Antennæ of
Moths.

The antennæ proceed from two points close to the upper
borders of the eyes. They are jointed organs, and are of very
different forms in the various species of Lepidoptera. They are
generally long, slender, and clubbed at the extremity in butterflies,
but exhibit several minor points of difference which we shall have to
note later on. In moths the antennæ are sometimes long, slender,
and pointed. Some are thick, and more or less prismatic in form;
while others are slightly or deeply pectinated or comb-like. The[Pg 6]
antennæ of butterflies are always straight, or only slightly curved;
and, although the insects can sway them bodily, they have no
power to bend them, or to stow them away in any place of shelter.
Moths, on the other hand, when at rest, are almost invariably found
to have their antennæ snugly tucked under the wings, and brought
so closely against the side of the head for this purpose that even
the uncovered portion is often difficult to find.

There are two other prominent appendages belonging to the
heads of the Lepidoptera. These are the labial palpi or feelers of
the lips. They are generally easily seen, projecting forward on the
under side of the head, sometimes so long and conspicuous as to
give one the idea of a snout or long nose. The palpi are
jointed—usually
in three parts—are covered with scales, and often furnished
with hairs or bristles.


Fig. 7.—Section
of the Proboscis
of a
Butterfly.

If you watch a moth or butterfly when it is feeding on the
sweet juices of a flower, or on some kind of artificial sweet with
which you have provided it, you will observe its long trunk or proboscis,
by which food is sucked up. This instrument is so long and
slender that it seems almost impossible that it can be a tube
through which a liquid freely passes. But a careful examination
will show that this is the case. It is composed of two separate
pieces—two half tubes, which, when closely applied to each other,
form a very thin and flexible pipe, perfectly air-tight and adapted
for suction. Sometimes you can see a butterfly or moth manipulating
with its proboscis as if it required readjustment in some way
or other. It has split the tube throughout its length, so that it now
looks like two exceedingly fine hairs. Then, after a short time, the
two halves are put together again, and immediately, as if by magic,
become a single tube in which no kind of seam is to be observed
without a powerful magnifier.

In order to observe the nature of such a wonderful arrangement
we must have recourse to the aid of a good microscope. Thus
assisted, we can see at once how the junction of the two sides of
the proboscis is brought about so quickly and so perfectly. The
inner edges of each half are very regularly fringed with lines of
closely set hairs—so regular, in fact, are they, that they give one
the idea of long yet minute beautifully formed combs. When the
two parts are brought together, the hairs of two opposite edges
interlock, those on one side exactly filling the spaces between those
of the other.

The microscope also reveals another interesting fact, viz. that[Pg 7]
the proboscis is not a single tube, but, although so remarkably thin,
is really a set of three distinct pipes, one lying on each side of the
central one. It is said that the central tube only is used for sucking
up the liquid food, and there seems to be some doubt as to the
uses of the other two. Some naturalists are of opinion that the
latter are air tubes, and are connected with the respiration of the
insect; while others say that through these the insects eject a thin
watery fluid with which to dissolve or dilute those sweetmeats
that are not sufficiently liquid to be readily sucked up. But possibly
both these opinions are correct, the proboscis serving all three
of the purposes here named. The only observation of my own
bearing on the subject is this. While a moth was feeding on a
drop of syrup in a strong light, a powerful lens revealed drops,
of liquid, mingled with bubbles of air, passing
alternately up and down the two lateral tubes of
the proboscis. At the same time the upward
current of syrup in the central tube was by no
means steady and continuous.

When this organ is not in use, it is beautifully
coiled into a close spiral which lies between the
labial palpi. The length varies considerably in
different insects, and consequently the number of
turns in the spiral must differ also. Sometimes
there are less than two turns, while some of the
longer ones form spirals of from six to ten turns.

In concluding our brief account of the head
of lepidopterous insects it is, I suppose, hardly
necessary to add that there is no kind of chewing
apparatus to be described; all the members of this order, at least in
the perfect state, deriving the whole of the little nourishment they
require entirely by suction through the proboscis or ‘trunk.’

The second division of the body is the thorax. This is much
larger than the head, and consists of three ring-like segments,
joined one behind the other so intimately that the lines of junction
are hardly visible, even after the thick clothing of fine hair has been
brushed off. Behind the thorax is the abdomen, which is composed
of several segments, the junctions between the rings often being
most distinct.


Fig. 8.—Diagram of the Wings of a Butterfly.

I. Fore wing.—1-5, subcostal nervules; 6, 7, discoidal nervules; 8-10, median
nervules; 11, submedian nervure; 12, internal nervure; 13-15, disco-cellular
nervules; 16, interno-median nervule; 17, median nervure; 18, subcostal
nervure; a, costal nervure; b, costa or anterior margin; c, apex or anterior
angle; d, posterior or hind margin; e, posterior or anal angle; f, interior or
inner margin; g, base; h, discoidal cell.

II. Hind wing.—1, 2, subcostal nervules; 3, discoidal nervule; 4-6, median
nervules; 7, submedian nervure; 8, precostal nervure; 9, subcostal nervure; 10,
median nervure; 11, 12, disco-cellular nervules; a, costal nervure; b, costa or
anterior margin; c, apex or anterior angle; d, hind margin; e, tail or caudal
appendage; f, anal angle; g, abdominal or inner margin; h, base.

From the sides of the thorax proceed the two pairs of wings, the
general structure of which we have already to a certain extent
examined. But when we are a little farther advanced in our[Pg 8]
insect studies, we shall have to become acquainted with detailed
descriptions given as aids to the identification of species. Now,
such descriptions cannot be satisfactory, either to the one who
gives or to him who receives, unless expressed in such definite
terms as render a misunderstanding impossible. A botanist cannot
give an accurate and concise description of a flower without the use
of certain names and expressions which have gradually become an
almost necessary part of his vocabulary; neither can an entomologist
give a really useful, and, at the same time, a succinct
description of an insect unless he is acquainted with the names of its
parts. Therefore, seeing that we distinguish the various species of
butterflies and moths mainly by the arrangement and colour of the
markings of their wings, it is really necessary that we should know
the names of the different parts of these organs. For this reason I
have inserted drawings of a fore and of a hind wing of a butterfly,
together with the names of the various parts of the wings, and also
the names of the principal rays or nervures. Yet I would not
advise any young entomologist to attempt to commit to memory
all the names given. Rather use the diagram for reference when
occasion requires, more particularly when you have an insect in
your possession that you desire to study. In ordinary descriptions
of butterflies and moths the names of the nervures are not so
generally used as those of the parts of the wing. Consequently it
is exceedingly useful to know what is meant by the terms base,
costal margin, apex, hind margin, anal angle, inner margin,
discoidal cell &c. as applied to the wing.

The two pairs of wings are attached to the second and third
segments of the thorax; but of the three pairs of legs, which we
have next to consider, one pair arises from each of the three
segments. The arrangement of these limbs is well shown in the
sketch on page 3, as are also the names of the different parts of
the limb, the latter being given for reference by the reader when
the need arises.

All insects, in their perfect state, we are told, have three pairs
of legs; but if you examine the under surface of certain butterflies,
such as the Marbled White, or any of the Vanessas, Browns, or
Heaths, it is quite likely that you will raise objection to such a
statement; for in these you may possibly see only four legs. But this
is the result of a too cursory observation. Look a little more closely
at your specimen, and you will see a pair of smaller legs folded
up under the fore part of the thorax. By means of a blunt needle[Pg 9]
you can straighten out these limbs, and then the difference in
length to be observed between them and the other four is very
striking indeed. They are also thinner than the middle and hind
legs; and, unlike these, are not provided with claws.


Fig. 9.—The Undeveloped
Fore Leg
of a Butterfly.

These imperfectly developed legs are, of course, quite useless as
far as walking is concerned; indeed, it is extremely doubtful as to
whether they are of any service whatever to the owner. On one[Pg 10]
occasion, however, while watching a Peacock Butterfly apparently
engaged in cleaning its divided proboscis, I observed that this organ
was frequently passed under the thorax, and that the front pair of
legs were pressed against it on each side, while it was being drawn
outward between them. It is probable, therefore, that these limbs
constitute a pair of brushes by means of which the fine grooves of
the divided trunk are cleared of any solid or sticky matter that may
lodge therein. It is certain that moths, and those butterflies that
possess six equal legs, use the front pair for this same purpose. The
former, also, employ them for brushing their antennæ, which seem
to be, by the way, particularly sensitive to different kinds of
irritation.

It is a well-known fact that tobacco smoke has a powerful
influence on certain small insects; and even though it can hardly
be regarded as a perfect all-round insecticide, it is certainly more
or less objectionable to the larger and hardier species. A short time
since, while watching a number of newly
emerged moths of the Sphinx group, and at
the same time enjoying the solace afforded by
the luxurious weed, a puff of the smoke was
accidentally allowed to play into the box in
which my pets were for the time imprisoned.
Immediately they rubbed their front legs
vigorously over the antennæ, as if to remove
the obnoxious irritant that had thus intruded on their presence.
Similar observations have led many naturalists to suppose that the
antennæ are the seat of various senses, such as those of touch,
hearing, and smell. Seeing that insects do not, as far as we know,
possess special organs for all the five senses which we enjoy (and it
is interesting to note here that some insects certainly experience
other sensations which are quite beyond our ken), we can quite
understand the common tendency to locate the seats of certain of
the senses in such easily affected parts as the antennæ. But little,
I believe, has been definitely proved save that the antennæ are
sensitive to touch and to irritants generally.

While speaking of the senses of insects, I cannot refrain from
mentioning a most remarkable example of a peculiar sensitiveness
that has been observed in certain moths of the family Bombyces
(page 217)—notably the Oak Eggar, the Emperor, and the Kentish
Glory. Take a newly emerged female of either of these species,
shut her up in a small box, conceal the box in your pocket, and then[Pg 11]
walk about in some country spot known to you as being one of
the haunts of that species of moth. Then, if any of the males of
the same species happen to be in the neighbourhood, they will
settle or hover about close to the female which, although still
concealed and quite out of their reach, has attracted them to the
spot.

What a marvellously acute sense this must be, that thus enables
the insects to scent out, as it were, their mates at considerable
distances, even when doubly surrounded by a wooden box and the
material of a coat pocket! You would naturally expect that
entomologists have turned this wonderful power to account. Many
a box has been filled with the beautiful Kentish Glories of the male
kind, who had been led into the snare by the attractions of a virgin
Glory that they were never to behold. Many an Emperor has also
been decoyed from his throne to the place of his execution, beguiled
by the imaginary charms of an Empress on whom he was never to
cast one passing glance. And these and other similar captures
have been made in places where, without the employment of the
innocent enchantress, perhaps not a single male could have been
found, even after the most diligent search.

Speaking of this surprising sense, I am again tempted to revert
to the antennæ; for it is a remarkable fact that the males of those
species of moths which exhibit the power of thus searching out their
mates, are just those that are also remarkable for their very broad
and deeply pectinated antennæ—a fact that has led to the supposition
that the power in question is located in the antennæ, and is
also proportional to the amount of surface displayed by these organs.

Up to the present time we have been considering the butterfly
and moth in their perfect forms, but everybody knows that
the former is not always a butterfly, nor is the latter always a
moth; but that they both pass through certain preparatory stages
before they attain their final winged state.

We shall now notice briefly what these earlier stages are, leaving
the detailed descriptions of each for the following chapters.

The life of the perfect butterfly or moth is of very short
duration, often only a few days, nearly the whole of its existence
having been spent in preparing itself for the brief term to be enjoyed

… in fields of light,
And where the flowers of Paradise unfold.

It may be interesting to consider of what use the metamorphoses[Pg 12]
of insects are, and to what extent these metamorphoses render them
fit for the work they have to do.

It is certain that the chief work of insects, taken as a whole, is
to remove from the earth the excess of animal and vegetable matter.
If they are to do this work effectually, it is clear that they must
be very voracious feeders, and also be capable of multiplying their
species prodigiously. Now each of these powers requires the special
development of a certain set of organs, and an abnormal development
of one set must necessarily be produced at the expense of the
other. Hence we find insects existing in two distinct stages, with
or without an intermediate quiescent state, during the first of which
the digestive apparatus is enormously developed, while the reproductive
organs occupy but very little space; then, during the other
stage, the digestive apparatus is of the simplest possible description,
and the organs of reproduction are in a perfect state of
development.

Allowing, then, that the chief work of the insect is the removal
of surplus organic matter, we can see that a large share of its life
should be spent in the larval or grub stage, and that the perfect
state need not occupy any more time than is necessary for the
fertilisation of the eggs that almost completely fill the body of the
female at the time of her emergence from the chrysalis shell.

Many insects undergo their metamorphoses by slow degrees,
but the Lepidoptera, after existing for some considerable period
without any important visible change in structure, pass by a rapid
transition into the next state. Thus, a caterpillar, that has not
altered in general form for several weeks, changes into a chrysalis
within the course of a few days; and again, after a period of quiescence
that may extend throughout the whole of the colder months,
becomes a perfect butterfly or moth within twenty minutes of the
moment of its emergence.

But this suddenness is more apparent than real, as may easily be
proved by internal examinations of the insect at various stages of
growth; showing that we are led astray by the rapidity of external
changes—the mere moultings or castings of the skin—while the
gradual transformations proceeding within are not so readily
observed.

We have already said that the life of the perfect butterfly or
moth is short. A few days after emergence from the chrysalis case,
the female deposits her eggs on the leaves or stems of the plant
that is to sustain the larvæ. Her work is now accomplished, and[Pg 13]
the few days more allowed her are spent in frolicking among the
flowers, and sucking the sweet juices they provide. But males
and females alike—bedecked with the most gorgeous colours and
overflowing with sportive mirth when first they take to the wing—soon
show the symptoms of a fast approaching end. Their colours
begin to fade, and the beauty-making scales of the wings gradually
disappear through friction against the petals of hundreds of flowers
visited and the merry dances with scores and scores of playful
companions. At last, one bright afternoon, while the sun is still
high in the heavens, a butterfly, more weary than usual, with heavy
and laborious flight, seeks a place of rest for the approaching
night. Here, on a waving stalk, it is soon lulled to sleep by a gentle
breeze.

Next morning, a few hours before noon, the blazing sun calls
it out for its usual frolics. But its body now seems too heavy to
be supported by the feeble and ragged wings, and, after one or two
weak attempts at play, incited by the approach of a younger and
merrier companion, it settles down in its final resting place. On
the following morning a dead butterfly is seen, still clinging by its
claws to a swinging stem, from which it is eventually thrown during
a storm.

The tale of the perfect moth is very similar to the above, except
that it is generally summoned to activity by the approach of
darkness.

We see, then, that butterflies and moths exhibit none of that
quality which we term parental affection. Their duty ends with
the deposition of the eggs, and the parents are dead before the
young larvæ have penetrated the shell that surrounds them.

Yet it is wonderful to see how unmistakably the females
generally lay their eggs on the very plants that provide the
necessary food for their progeny, as if they were not only conscious
of and careful concerning the exact requirements of their offspring,
but also possessed such a knowledge of botanical science as
enabled them to discriminate between the plant required and all
others.

Has the perfect insect any selfish motive in this apparently
careful selection of a plant on which to lay its eggs? Does the
female herself derive any benefit from the particular plant chosen
for this purpose? In most cases, certainly not. For it often
happens that the blossom of this plant is not by any means one of
those that supply the sweets which insects love, and still more[Pg 14]
frequently does it occur that the eggs are deposited either before
the flowers have appeared or after they have faded.


Fig. 10.—The Four Stages of the
Large White Butterfly (Pieris
Brassicæ).

a, larva; b, pupa; c, imago; d, egg.

Neither can we easily impute to the insect an acquired knowledge
of the nature and wants of her offspring, or an acquaintance
with botany sufficient to enable her to distinguish plant
forms. Our only solution of the problem (which is really no solution
at all) is to attribute the
whole thing to that inexplicable
quality which we are pleased
to term natural instinct. It
is to be observed, however, that
it is not all butterflies and
moths that display this unerring
power. Some few seem to
deposit their eggs indiscriminately
on all kinds of herbage.
But, I believe, the larvæ of
these species are generally
grass feeders, and would seldom
have to travel far from
any spot without meeting with
an acceptable morsel.

But we must now pass on
to a brief consideration of the
other stages of the insect’s
existence. After a time, varying
from a few days to several
months, the young caterpillars
or larvæ make their appearance.
They soon commence
feeding in right earnest. Their
period of existence in this state
varies from a few weeks to
several months, and even, in
some cases, to years. During this time their growth is generally
very rapid, and they undergo a series of moults or changes of skin,
of which we shall have more to say in a future chapter. Then,
when fully grown, they prepare for an apparently quiescent form,
which we speak of as the pupa or chrysalis, and in which they
again spend a very variable period, extending over a few days,
weeks, or months. Now, inclosed in a protective case, each pupa[Pg 15]
is undergoing a remarkable change. Some of its old organs are
disappearing, and others are developing; and, after all the parts of
the future insect have been developed as far as its narrow shell will
permit, it bursts forth into the world as a perfect insect or imago.

Its wings at first are small, shapeless, and crumpled in a most
unsightly fashion; but it is not long before they assume their full
size, beautiful form, and gorgeous colouring. Then, in about
another hour or two, the wings, at first soft and flaccid, have
become sufficiently dry and stiff to bear their owner rapidly
through the air.

We have thus observed some of the more striking features in
the structure of the butterfly and moth in its most perfect state;
and alluded in a very brief manner to the various stages through
which these creatures must necessarily pass before finally reaching
this stage. But now we must study these earlier stages more
closely, and watch the insects during the marvellous transitions
they are destined to undergo. This we shall do in the following
chapters.


[Pg 16]

CHAPTER II

THE EGG

I suppose you are all acquainted with the general structure of the
hen’s egg, having dissected several, in your own way, many a time.

Its outer covering, which you speak of as the ‘shell,’ you have
observed is hard and brittle. It is composed of a calcareous or limy
substance, known chemically as carbonate of lime. If you put
some pieces of it into an egg cup, and throw over them a little
vinegar or any other liquid acid, you will see them gradually
dissolve away, and small bubbles of carbonic acid gas will rise into
the air. Then again, if you take a long and narrow strip of the
shell, and hold one end of it in a gas or lamp flame, after a short
time that end will become softer, and will glow brightly in the
flame, for it is converted into lime—the same substance that is
used by the builders for making their mortar—and the bright glow
is really a miniature lime light, such as is always produced when a
piece of lime is made intensely hot.

Just inside this shell you have seen a thin membrane or skin
that is easily peeled off the substance of the egg itself. Next to
this comes the ‘white’ of the egg, which is really colourless while
liquid, but turns white and more or less solid in the cooking. Last
of all, in the centre of this, you have noticed the oval yellow mass
that is termed the ‘yoke’ or ‘yolk,’ and which contains the
embryo of the future chick.

Now if you imagine this egg to be reduced in size till two or
three dozen of them would be required to form a single line about
one inch long, the outer calcareous shell to be entirely removed, the
skin or membrane to be converted into a firmer substance of a
horny nature, and, finally, the yolk to be absent and the whole
internal space to be filled with the ‘white,’ you will then have some
idea of the nature of the egg of a butterfly or moth.[Pg 17]

To put the matter more briefly, then, we will say that the eggs
of these insects are simply little liquid masses, usually of a colourless
substance, surrounded by a horny and flexible covering.

Such a description may certainly give you some idea of
the nature of the eggs of insects, but no amount of book reading
will serve the purpose so well or be so pleasant as the examination
of the eggs themselves. During the summer months
very little difficulty will be experienced in finding some eggs
in your own garden. Turn over some leaves and examine their
under surfaces, choosing especially those plants which show, by
their partially eaten leaves, that they are favourites with the insect
world. Or you may amuse yourself by catching a number of butterflies—common
‘Whites’ are as good for the purpose as any—and
temporarily confine them in a wooden or cardboard box, containing
a number of leaves from various plants, and covered with gauze.
In this way you are sure to obtain a few females that have not yet
laid all their eggs; and if you watch your prisoners you will soon
see them carefully depositing the eggs on the under surfaces of
leaves, bending their abdomens round the edges if there is not sufficient
room to get themselves completely under. And then, when
you are satisfied with the number of eggs thus obtained for your
examination, you can have the pleasure of seeing all your liberated
captives flying joyfully in the free air.

In giving these simple instructions I have assumed that the
reader has not yet learnt any of the characters by which female
butterflies are to be distinguished from their lords and masters; but
I hope that he will know soon, at least with regard to a good many
species, from which individuals he may most reasonably expect to
obtain eggs, and so be able to avoid the imprisonment, even though
only temporary, of insects which cannot satisfy his wants.

Again, it is not necessary, after all, that butterflies should be
captured for the purpose of obtaining eggs. Watch them as they
hover about among your flowers. Some, you will observe, are intent
on nothing but idle frolicking; and you may conclude at once that
these have no immediate duty to perform. Others are flying without
hesitation from flower to flower, gorging themselves with the
sweets of life: these are not the objects of your search. But you
will descry certain others, flying round about the beds and borders
with a steadier and more matronly air, taking little or no notice of
their more frivolous companions, and paying not the slightest heed
to the bright nectar-producing cups of the numerous flowers. These[Pg 18]
are seriously engaged with family affairs only. Watch one of them
carefully, and as soon as she has settled herself on a leaf, walk steadily
towards her till you are near enough to observe her movements.
She will not move unless you approach too closely, for, like busy
folk generally, she has no time to worry about petty annoyances.
You will now actually witness the deposition of the eggs exactly as
carried on in the perfect freedom of nature; and the eggs themselves
may be taken either for examination or for the rearing of the
caterpillars.

Some species of Lepidoptera lay some hundreds of eggs, and it
is seldom that the number laid by one female is much below a
hundred.

As already stated, the under surfaces of leaves are generally
chosen for the deposit of eggs, but a few of the insects we are considering
always select the upper surface for this purpose. Thus
the Puss Moth (page 235), and two or three others resembling it,
though much smaller, known as the Kittens (page 234), invariably
lay them on the upper surface. And this is the more surprising
since the eggs of these moths are brown or black, and consequently
so conspicuous on the green leaves as to be in danger of being
sighted by the numerous enemies of insects.

The Hairstreak Butterflies (page 183) afford another exception to
the general rule, for their eggs are deposited on the bark of the trees
and shrubs (birch, sloe, elm, oak, and bramble) on which their
larvæ feed.

At the moment each egg is laid it is covered with a liquid
sticky substance, so that it is immediately glued to the leaf or stem
as soon as it is deposited. The sticky substance soon dries, causing
the egg to be so firmly fastened in its place that it is often impossible
to force it off without destroying it completely.

Some of the Lepidoptera deposit their eggs singly, or in small
irregular clusters; but by far the larger number set them very
regularly side by side, in so compact a mass that it would be
impossible to place them on a smaller area without piling one on
top of another. This is not accomplished with the aid of the sight,
for the insect performing her task with such precision often has her
head on one side of a leaf or stem while arranging her eggs on the
other. If you take the trouble to watch her, you will see that she
carefully feels out a place for each egg by means of the tip of her
abdomen immediately before laying it.

The eggs are laid by moths and butterflies at various seasons[Pg 19]
of the year. In some cases they are deposited early in the spring,
even before the buds of the food plants have burst; and the young
larvæ, hatched a few weeks later, commence to feed on the young
and tender leaves. Then, throughout the late spring, the whole of
the summer and autumn, and even till the winter frosts set in, the
eggs of various species are being laid.

Those deposited during the warm weather are often hatched in
a few days, but those laid toward the autumn remain unchanged
until the following spring.

In this latter case the frosts of the most severe winter are not
capable of destroying the vitality of the eggs. In many instances
the perfect insect or the larva would be killed by the temperature
of an average winter day, but the vitality of the eggs is such that
they have been subjected to a temperature, artificially produced, of
fifty degrees below the freezing point, and even after this the young
larvæ walked out of their cradles at their appointed time just as if
nothing unusual had occurred.

Experiments have also been performed on the eggs with a view
of determining how far their vitality is influenced by high temperatures.
We know that the scorching midsummer sun has no
destructive influence on them, but these experiments prove that
they are not influenced by a temperature only twenty degrees below
the boiling point—actually a considerably higher temperature than
is necessary to properly cook a hen’s egg.

Let us now examine a number of eggs of different species, that
we may note some of the many variations in form and colour.

With regard to colour, we have already observed that the eggs
of a few species are black; but more commonly they are much
lighter—pearly white, green, yellow, and grey being of frequent
occurrence.

The great variety of form, however, will provide a vast amount
of enjoyment to anyone who possesses a good magnifying lens or
a small compound microscope. Some are globular, others oval;
while many others represent cups, basins, and domes. Then we
have miniature vases, flasks, bottles with short necks, and numerous
figures that must remind a juvenile admirer of the sweet
cakes and ornamental jellies that have so often gladdened his
longing eyes.

Again, the beautifully sculptured surfaces of a large number are
even more striking than their general shapes. Some are regularly
ribbed from top to bottom with parallel or radiating ridges, and at[Pg 20]
the same time marked with delicate transverse lines. Others are
beautifully pitted or honeycombed, some ornamented with the
most faithful representation of fine wicker-work, while a few are
provided with a cap, more or less ornamental, that is raised by the
young larva when about to see the world for the first time. A few
of these beautiful forms are here illustrated and named, and another
has already appeared on page 14, but an enthusiastic young
naturalist may easily secure a variety of others for his own
examination.


Fig. 11.—Egg of
the Meadow
Brown Butterfly.

Fig. 12.—Egg of
the Speckled
Wood Butterfly.

Fig. 13.—Egg of
the Vapourer
Moth.

It may be surmised from the accompanying illustrations that
the form of the egg is always the same for any one species.
This is really the case, and consequently an experienced entomologist
can often decide on the name of the butterfly or moth that
deposited a cluster of eggs he happens to find in his rambles and
searchings; but in such decisions he is always greatly assisted by a
knowledge of the food plants of the various insects, and sometimes
also by the manner in which the eggs are arranged.

We have seen that the period during which the Lepidoptera
remain in the egg stage is very variable, and depends largely on
the season in which they were laid; but it is often possible to tell
when to expect the young larvæ by certain changes which take
place in the appearance of the egg. As the horny covering of
the egg is transparent, the gradual development of the caterpillar
from the clear fluid can be watched to a certain extent; but
if you have a microscope, and would like to witness this development
to perfection, proceed as follows.

Arrange that some butterflies and moths shall lay their eggs on
strips of glass of convenient dimensions for microscopic work—three
inches long by one wide is the usual size for this kind of work.
This is easily accomplished by placing a proper selection of female
insects in a rather small box temporarily lined with such ‘slips.’
When a few eggs have thus been secured, all you have to do is[Pg 21]
to examine them at intervals with your microscope, always using
the reflector so as to direct a strong light through the eggs
from below.

But even without such an arrangement some interesting
changes are to be observed. As a rule, the colour of the egg
turns darker as the time for the arrival of the infant larva approaches,
and you will often be able to see a little brown or
black head moving slightly within the ‘shell.’ You may know
then that the hatching is close at hand, and the movements of
the tiny creature are well worth careful watching. Soon a small
hole appears in the side of the case, and a little green or dark
cap begins to show itself. Then, with a magnifier of some kind,
you may see a pair of tiny jaws, working horizontally, and not
with an up-and-down motion like our own, gradually gnawing
away at the cradle, till at last the little creature is perfectly free to
ramble in search of food.

Strange to say, the young larva does not waste a particle of
the horny substance that must necessarily be removed in securing
its liberty, but devours it with an apparent relish. Indeed, it appreciates
the flavour of this viand so highly that it often disposes
of the whole of its little home, with the exception of the small
circular patch by which it was cemented to the plant. When the
whole brood have thus dispensed with their empty cradles, there
remains on the stem or leaf a glittering patch of little pearly
plates.

After the performance of this feat the young caterpillar starts
off in life on its own account with as much briskness and confidence
as if it had previously spent a term in the world under the same
conditions; but we must reserve an account of its doings and sufferings
for our next chapter.


[Pg 22]

CHAPTER III

THE LARVA

In almost every case the young caterpillar, on quitting the ‘shell’
of the egg, finds itself standing on and surrounded by its natural
food, and immediately commences to do justice to the abundant
supply. It will either nibble away at the surface of the leaf, removing
the soft cellular substance, so that the leaf exhibits a number of
semi-transparent patches when held up to the light, or it will
make straight for the edge, and, closing its horizontal
jaws on either side, bite the leaf completely
through, and thus remove a small piece each time.


Fig. 14.—The
Caterpillar of
the Clouded
Yellow Butterfly.

Several naturalists have amused themselves by
performing experiments and making calculations
on the efficiency of the masticating and digesting
powers of the caterpillar. The illustrious Réaumur,
for example, proved that some of the cabbage
eaters disposed of more than twice their own
weight of food in twenty-four hours, during which
time their weight increased one-tenth. Let us see
what this would be equivalent to in human beings:
A man weighing eleven stone would devour over
three hundred pounds of food in a day, and at the
end of that day weigh about fifteen pounds more
than he did at the beginning!

So the young caterpillar eats, and rests, and
grows, till, while still young, its body has become too large for the
already tightened skin. It evidently feels very uncomfortable. Its
appetite fails, and it remains for a time perfectly quiet in one spot,
having previously spun a little carpet of silk to form a firm foothold
during its temporary indisposition. Its colours have also
become dingy, and anyone, not understanding the character of its[Pg 23]
growth, might easily be led to suppose that the poor creature was
displaying the earlier symptoms of a serious and perhaps fatal
illness.

But soon an encouraging symptom is observed. The caterpillar
begins to get restless. Its front segments are turned alternately
right and left, and are also made to swell out much beyond their
normal size. Then in a very short time—often less than a minute
from the first appearances of restlessness—the skin, which has
become somewhat dry and brittle, splits along the back over the
second, third and fourth segments, revealing a new and bright coat
beneath. The caterpillar continues its struggles and, in addition
to the previous movements, causes the swelling to move backward
along the body. This, acting like a
wedge, causes the rent in the old coat
to extend in that direction.


Fig. 15.—The Caterpillar of
the Dark Green Fritillary
Butterfly.

The caterpillar now draws its head
backward, and, with a few convulsive
struggles, pulls the front segments
out of their old skin, and passes its
head out of the rent in the back.
With its foremost segments thus
rendered perfectly free, it walks
straight out of the old garment,
which is left still fixed by the legs to
the silken carpet.

The larva, although now fresh and smart in its appearance, is
exhausted by these struggles and its prolonged fast. The new skin,
moreover, is very soft and tender, even to the cases of the head
and legs, which are normally very hard. But a short period of
rest suffices to dry its skin and sharpen its appetite, and then it
eats more vigorously than ever.

We will now leave the caterpillar for a moment while we look
at its cast-off clothes. They are still clinging to a stem so firmly
that they can scarcely be removed without injury. The hard shell
that covered the head and jaws is perfect in form, and so are the
claws and cases of the legs. All the hairs or spines that happened
to adorn the previous owner still retain their positions; and the
whole skin, although always more or less shrivelled, is sometimes
so slightly altered in form that it might be mistaken for a living
caterpillar if not closely examined.

But this is not all. For, according to the accounts of some[Pg 24]
authoritative observers, the lining of the digestive organs, which is
really a continuation of the outer skin, is cast off (or rather cast
out) at the same time, as are also the linings of the larger breathing
tubes which are presently to be described.


Fig. 16.—The Caterpillar
of the
Purple Emperor
Butterfly.

We have seen that some caterpillars, on quitting their egg cases
(which may really be regarded as the first moult), make their first
meal of the old covering. So also some of them, in their future
moultings, exhibit an apparently useless economy (seeing that they
are surrounded by an abundance of their
natural vegetable diet) by devouring their
old coats! In the face of this fact we can
hardly describe them as strict vegetarians.

Having thus passed through its first hardship,
the caterpillar has by no means seen
the end of the troubles and dangers that beset
it; for, during its existence in the larval state,
it has to go through a series of three, four, five,
or even six moults, all of which are periods
of considerable inconvenience, and perhaps
even pain, and frequently prove fatal. And
it is by no means an uncommon thing to
meet with the lifeless body of an unfortunate
individual who, as shown by its shabby
appearance and the silken carpet under its
feet, has evidently fallen a victim to the
dangerous process of ridding itself of an old garment.

But this is only one of the many dangers to which caterpillars
are exposed. Throughout every hour of the day the sharp and
hungry eyes of the numerous insect-eating birds are searching the
leaves for such delicacies to satisfy the wants of themselves and
their broods. The lively little lizards, too, during the sunny
hours are busily engaged in searching them out among the foliage
of heaths and banks.

Very formidable enemies also exist in the form of Ichneumon
and other species of flies, which pierce the skins of caterpillars with
their sharp ovipositors, and lay their eggs within the bodies of
the unfortunate victims. As soon as the young larvæ are hatched
from these eggs, they commence feeding on the fatty substance
stored beneath the caterpillar’s skin. They carefully avoid, at
first, attacking the vital organs of their host’s body, and in this
way secure for themselves a more lasting supply of fresh food.[Pg 25]
When the fatty substance is nearly all gone, they eat their way
into the more important structures, of course steadily growing all
the time; and so, even though the body of the caterpillar is rapidly
diminishing, the total bulk shows often no very appreciable decrease
in size. When the larvæ of the flies are fully fed, they either
change to the pupa within the carcase of their host, or eat their
way out of its body and construct for themselves a cocoon in which
to undergo the transformation.


Fig. 17.—An Ichneumon Fly
(Cryptus Migrator).


Fig. 18.—Another Ichneumon
Fly (Pimpla Instigator).

As for the caterpillar itself, it sometimes dies before the time
for its metamorphosis has arrived; but it often changes to the
chrysalis before its fate is sealed. In this latter case, a number of
flies, having undergone their final transformation within the
chrysalis shell (there being but little else than shell remaining
of the victim’s body), break forth from the remains of the carcase
somewhere about the time at which the butterfly or moth should
have appeared.

Caterpillars have also their nocturnal enemies and devourers,
among which may be mentioned frogs, toads, newts, and insect-eating
mammals.

We must now learn something of the structure of caterpillars;
and then become acquainted with their habits, and the change to
the chrysalis or pupa.

Take a caterpillar from your garden, preferably a full-grown
one of a rather large species, that is not very densely covered with
hair, and examine it carefully as we note the main points in its[Pg 26]
structure. The first point that strikes our notice is the division of
its body into segments or rings, separated from each other by a
more or less distinct line or slight constriction of the body.

There are thirteen of these segments, reckoning, as is usual, the
head as the first.

The head is usually very hard, and often of a much darker
colour than the rest of the body. It is also frequently divided into
two lobes by a couple of oblique lines, between which the parts of
the mouth are situated. The two powerful horizontal jaws, to
which we have already referred, are very hard and sharp, and
curved like a sickle, and therefore splendidly adapted for biting from
the edges of leaves. The head is also provided with a pair of
antennæ, usually very short and inconspicuous and protected by a
horny covering.

Unlike the perfect insect, the caterpillar has no large compound
eyes, but twelve very small simple eyes, situated on the cheeks,
very near the mouth—six on each
side.


Fig. 19.—The Caterpillar of
the Angle Shades Moth
(Meticulosa).

If you examine them with a magnifier,
you see that each one is provided
with a small and very convex
lens—a lens of very short focus, such
as would be used for the examination
of small objects held very near to
the eye. From this arrangement we should be inclined to conclude
that the caterpillar can see only those objects that are
close to its mouth; and this idea is strengthened if you place
one in a box containing a number of leaves, one of which is
that of its own food plant. It will wander about the box, apparently
looking at every part of every leaf it passes, after the
manner of a very short-sighted individual, and never taking a
general look round. A butterfly or a moth can see a flower in
the distance, for it flies unhesitatingly from one to another in
the straightest and shortest path, but if you place a caterpillar
in the centre of a ring composed of a leaf of its food plant and
nine others from other plants, the chances are (nine to one) that it
will not walk towards what it would like to have.

Again, the eyes are situated on the lower part of the cheek,
directed slightly downward, and are therefore adapted for seeing
what is just under its jaws as it walks along. Had we no knowledge
whatever of the caterpillar’s twelve little eyes, we should probably[Pg 27]
have thought that it sought out its food by some sense other than
that of vision.

Another important and interesting feature of the head is the
silk-spinning apparatus, situated under cover of the lower lip. This
consists of two tubular glands, corresponding to our own salivary
glands, the special purpose of which is to secrete a viscid fluid that
solidifies on exposure to air. The opening by which the fluid
escapes is so situated that the caterpillar can easily apply it to the
surface of any object over which it is walking, and then, by drawing
or turning away its head, cause a silken fibre to be produced.

Some caterpillars make use of this spinning apparatus only on
a few special occasions, but others, more especially some of the
smaller species, seem to have it always in use, so that if at any
time you suddenly start them into the air by giving a smart tap to
the plant or twig on which they rest, they invariably fall slowly on
the end of a growing web, the spinning of which they stop as soon
as they consider they have fallen far enough. Sometimes, as you
are walking through a wood, you will see hundreds, nay, thousands
of little caterpillars thus suspended, swinging gently in the
breeze. Not long since, after only a few minutes’ walk among the
trees of Epping Forest, I found I was decorated with several dozens
of these swingers with which I had come into collision—in this
case consisting chiefly of the larvæ of the Green Tortrix Moth
(Tortrix viridana).


Fig. 20.—Walking Leg
of a Caterpillar.

Now let us examine the caterpillar’s limbs. Attached to each
of the second, third, and fourth segments is a pair of true walking
legs, corresponding with those of the perfect insect. These are
covered with a hard and shining substance, and are also each
provided with a hook. The fifth and sixth segments have no limbs
at all, nor have the eleventh and twelfth, but some or all of the
others (seventh, eighth, ninth, tenth, and thirteenth) are furnished
with a pair of claspers which we shall presently describe.

First, as regards the number of claspers, it will be seen from
what has just been said that this is not always the same. Some
caterpillars possess five pairs, thus making up the total number of
walking appendages to sixteen. In fact, we must regard this as the
usual number. But there are at least a few hundred exceptions to
the rule. Many of the Bombyces (page 217), for example, have only
four pairs of claspers; and in others of the same group the fifth
pair is present, but only partially developed, and quite useless for
walking.[Pg 28]



Fig. 21—Larva of the Yellow Underwing
Moth (Pronuba).

Fig. 22.—Larva of the
Crimson Speckled
Moth (Pulchella).

Fig. 23.—Larva of the Lobster Moth
(Fagi).

Look at the peculiar caterpillar of the Lobster Moth (fig. 23)—a
creature that differs from most other caterpillars not only in its
claspers, but in many other respects too. Observe its long and
slender legs, its humped middle segments, and its upturned hindermost
segment, of enormous size and mounted with a pair of
clubbed ‘horns.’ This last segment you will observe, has no
claspers.

Another allied caterpillar is that of the Iron Prominent Moth
(fig. 24). This one also has humped segments, and the claspers of
the thirteenth segment are imperfectly developed.

A large number of other exceptions to the general rule are to be
found in the caterpillars of the Geometer Moths (page 268), one of
which is here represented. These have generally only two pairs of[Pg 29]
claspers, one pair on each of the tenth and last segments, so that
there is a distance equal to the combined length of six segments
between the hindermost true leg and the first pair of claspers. But
even among the Geometers there are variations to be observed in
the number of claspers, and some of these will be pointed out in our
brief descriptions of the commoner species.



Fig. 24.—Caterpillar of
the Iron Prominent
Moth (Dromedarius).


Fig. 25.—Larva of the Brimstone
Moth (Luteolata).

These limbs which we have been calling claspers are known by
several other names. Thus they are termed ‘pro-legs,’ ‘temporary
legs,’ ‘false legs,’ and ‘abdominal legs;’ but if you watch a
caterpillar as it walks up a stalk or along the edge of a leaf,
you will certainly agree that the term ‘clasper’ is everything that
could be desired. But why not call them legs, seeing that they
are used in walking? The reason is that they differ in many
respects from the three foremost pairs of
limbs as regards structure, persistency, and
function. The true legs, as we have called
them, continue to exist, though concealed, in the chrysalis state,
and again appear, far more perfectly developed, in the butterfly
or moth, but the claspers are no more to be seen after the
caterpillar has passed into the quiescent stage. We have noticed,
too, that the true legs are pointed and clawed, also that they are protected
by a hard and horny covering; but examine a large caterpillar,
holding it between the fingers and thumb with its under side
uppermost, and you will soon see that the claspers are not at all hard,
but soft and fleshy; not pointed, but often terminating in a broad
flat circular surface. You will also observe, as the creature struggles
to escape from your grasp, and tries to get a hold on something with
its claspers, that these limbs, if we may so call them, are retractile,
and are sometimes completely drawn into the body. Finally,
examine the broad end of a clasper with a magnifier, and you will[Pg 30]
see it surrounded by a circle of little hooks, turning in all directions.
You will no longer wonder how it is that a caterpillar can hold so
tenaciously to a piece of twig that it is often almost impossible
to remove it without injury.

Now put your caterpillar down, so that you may observe its gait.
If it happens to be one with the full complement of sixteen limbs,
you see that at each stride it makes but little progress. The
segments contract and relax alternately and in succession, thus
sending a series of wave-like motions along the body, and urging
onward the front segments while the claspers keep the hinder
portion firmly fixed.


Fig. 26.—The Claspers
of a Caterpillar.

But if your caterpillar is one of the Geometers, with only two,
or perhaps three, pairs of claspers, the mode of procedure is very
different. The creature stretches its body out at full length, often
raising its head high in the air, and swinging
its long body right and left with a most
furious motion, as if to hastily scan the
neighbourhood. Then, having satisfied
itself as to the direction of its proposed
course (which, by the way, is often changed
considerably at almost every stride), it
holds on by the true legs and pulls its
hinder quarters forward till the body forms
almost a closed loop, with the fourth segment
nearly touching the ninth. The
claspers now become the holdfasts. The
little hooks with which they are provided
are firmly fixed to the surface on which it is walking; and the
body being again straightened out to its utmost length, the same
manœuvre is repeated. So, you see, the insect progresses by
strides equal in length to about six segments of the body, and
these the longest segments generally; and the rate at which the
strides succeed each other, especially in some of the smaller species,
is really astonishing.

We have seen the caterpillar in the act of taking its walk, and
now we will give it a twig of its food plant so that we may see it
feed. It walks up the twig without hesitation—for caterpillars
(excepting those which feed on roots) always seem to move upward
when in search of food—and soon finds itself on a leaf. Over this
it walks till it reaches the edge; and, grasping the edge firmly
between the claspers, so as to give perfectly free play to its legs and[Pg 31]
head, it stretches its body at full length, and takes a series of bites
as it brings its head backward in a curve. When the head has
thus been brought close to its fore legs, the body is again extended,
and the same ground is gone over again.

If the caterpillar is a fairly large and hardy one, it will bite
through the smaller veins, and perhaps even the larger ones; but
the smaller species often change their position on reaching a
moderately thick vein, and so devour little else than the soft cellular
substance of the leaf. In any case, it is astonishing to see how
rapidly the leaf disappears under the influence of the powerful jaws
and marvellous digestive apparatus of the hungry grub.

Those who take a delight in watching the movements of caterpillars
are sure to be interested in observing them when at rest;
for at such times the various attitudes assumed are as pleasing
and instructive as are their active moments. And these attitudes
are all the more interesting on account of the mimicry by which
the creatures often baffle their numerous enemies. We may
profitably spend a little time in studying a few cases in point.

Many species, when at rest, fix themselves by means of their
claspers to a small twig or leaf stalk, or on the midrib of the leaf
itself. Here they remain perfectly still, with their bodies perfectly
straight or with head slightly raised. I need hardly say that these
generally fix themselves on the under side of the leaves and stalks,
thus securing themselves against the attacks of the feathered foes
above. But some birds are equal to the caterpillars in this matter;
and it is really amusing to see them hopping about beneath the
leaves in our gardens, every now and again slyly turning one
eye upward, and smartly plucking an unwary grub from its resting
place.

The precautions of the caterpillar, however, do not end merely
with the selection of an under surface. You will find that the
bright green species invariably settle on a leaf or a green stalk,
while the darkly coloured insects often choose a twig covered with
a brownish bark. Some even make for the trunk of the tree on
which they feed, and here remain quite still in a vertical position,
so that they look just like a ridge in the bark, the colour of which
is faithfully imitated by their skin. Further, many of the caterpillars
that resort to this stratagem have bodies that are notched
or knotted and spotted in such a manner that the resemblance to
their surroundings is so perfect as to defy any but the most
experienced eye. And even this is not all, for a number of these[Pg 32]
mimics of the insect world never venture to feed by day, but take
in their quantum of provisions during the dark hours, and practise
their deceptions throughout the day.

Most of the Geometer caterpillars, of which we have already
spoken, are well trained in the art of deception. You are out
on a caterpillar hunt, and engaged in carefully turning over the
twigs of the hazel or some other shrub, so that you may the more
readily examine the under surfaces of the leaves. At last you lay
hold of a small broken twig for this very purpose. To your
astonishment it is very soft, and readily bends between your
fingers. You look more closely at this peculiar piece of stick, and
find, to your surprise, that you have grasped a looper caterpillar
that was standing out at an angle just like a broken twig,
supported by its two pairs of claspers, and coloured and knotted
exactly like the little branch on which it rested.

At other times you meet with little green caterpillars of the
same group, supporting themselves in exactly the same manner on
a small twig, and looking just like a leaf stalk from which the
blade had fallen or been devoured.

What a wonderful power is exhibited in the grasp of the
claspers and the tension of the muscles, enabling the caterpillar to
fix itself and retain its position for so long a time! Imagine an
acrobat fixing himself by his hands on an upright pole, throwing
out his body at an angle, and without any further support retaining
his position motionless for several hours!

Other experiences of the larva hunter are equally interesting
and, perhaps, even more tantalising. He is engaged in very
cautiously turning over the leaves of a certain food plant from
which he hopes to obtain the larva of a much-coveted species.
Then, just as his eye catches a glimpse of the very object of his
search, down falls the caterpillar, rolled up into a little ball, among
the herbage below. This latter is diligently and patiently examined.
But no, the anticipated prize is nowhere to be seen.
It is probably a green one, and this adds to the difficulty of the
patient entomologist. Then, as he carefully separates the low
herbs, hoping to find the spot where the larva had fallen, the
insect, rolled up into a compact little ball, only sinks deeper and
deeper into the maze.

Many caterpillars avoid capture in this manner, while others
seek to avoid detection by remaining perfectly motionless, even
when roughly handled. They allow themselves to drop from their[Pg 33]
resting place on the slightest sign of danger, and, when the alarm
is over and all is quiet again, they ascend the food plant and
resume their position.

Some caterpillars not only rest, but even feed under cover,
quite secure from most, if not all, of their enemies. Several of
them feed on roots, and many a farmer can relate sad experiences
of the havoc committed by these caterpillars on his turnips and
other crops. Then there are those which feed on flowers and buds,
completely burying themselves in the dense mass of food.


Fig. 27.—The Homes of Leaf Miners and Leaf Rollers.

We must conclude this brief account of resting and hiding
places and attitudes of caterpillars by a few observations on the
leaf miners and leaf rollers.

The former are very small caterpillars—the larvæ of certain
small moths—that eat burrows into leaves without doing any considerable
injury to the outer epidermis, and thus prepare a safe
resting place within the substance of their food.

The latter, also mostly of small size, make themselves secure
by curling a leaf or a portion of a leaf into a cylinder, and holding
it in position by means of a number of silken threads.

If you examine a leaf thus curled you will soon be convinced[Pg 34]
that a considerable number of the extremely delicate threads must
be necessary to hold it in position; but, if you would like to know
how a very small and feeble caterpillar can manage to roll up a
comparatively large and rigid leaf, you must watch the little creature
at its work.

You need have but little difficulty in finding a willing worker,
for such caterpillars are extremely numerous. Take a few out of
their self-made homes, place them on a sprig of the food plant,
and you will soon have the pleasure of seeing one start its extraordinary
work.

At first it spins a number of threads stretching from the edge of
a leaf to about the middle of the surface. These threads are not
tight by any means, and the leaf is, as yet, unchanged in position.
But now the little mechanic exhibits a tact that almost seems to
prove a knowledge of the principles of its art. Each thread in turn
is pulled at right angles at its middle, and then fastened by means
of the creature’s spinneret. Each time this is done the edge of
the leaf is bent round a little; and when at last the cylinder is
completed, a number of other threads are stretched across from the
scroll to the flat part of the leaf to secure it firmly in its place.

Many caterpillars are solitary in their habits: that is, they are
always found singly, whether walking, resting, or feeding. But a
large number of species are gregarious, living in dense clusters
either throughout their larval state or, perhaps, only while young.
In many such cases it is difficult or even impossible to find any
reason for this gregarious tendency—to discover any advantage
that the insects may derive from the habit. Many species, however,
are true co-operators in the defence of their communities.
The caterpillars of such live in clusters, sometimes several scores
in each, and all help in the spinning of a complicated mass of silk
fibres, which, with the leaves and twigs they join together, form a
safe home in which they can rest, feed, or change to the chrysalis
state. In early summer hundreds of such caterpillar ‘nests’ are
to be seen in many of our hawthorn and other hedgerows.

Before closing our general account of the caterpillar we must
have a word to say about the breathing apparatus, more especially
as in our future descriptions we shall frequently have to mention
the colours and markings which surround the openings in its body
through which the air supply is admitted.

If you examine the sides of the segments of a caterpillar, using
a lens if the insect is a small one, you will observe some little[Pg 35]
round holes, often inclosed in a ring or a patch of some prominent
colour. These are the spiracles or openings of a series of air tubes
called tracheæ. These latter divide and subdivide within the body
of the caterpillar, the branches of one often uniting with those of
another, thus forming a really complicated arrangement of air pipes
by which the supply of oxygen is distributed.

A microscopic examination of a portion of one of the tracheæ
will show that its walls are supported by an elastic spiral of a firm
substance. This arrangement serves to keep the air passages open,
and secures for the caterpillar a free supply of air at times when a
contraction of the segments would otherwise cause the tubes to
collapse.

There are nine spiracles on each side of the caterpillar’s body,
and never more than one in the side of the same segment. The
head, which we have been regarding as the first segment, has no
spiracles. The second segment has a pair—one on each side.
There are none in the third and fourth; but all the segments, from
the fifth to the twelfth inclusive, have each a pair; the last
(thirteenth) segment has none.

We have already observed the general arrangement of the caterpillar’s
limbs; but perhaps it may be interesting and even convenient
to the reader to give here a little table that will show at a
glance the disposition of both limbs and spiracles.

Firstsegment—headTwo short antennæ, two jaws, and twelve eyes.
Second ”Legs and spiracles.
Third ”Legs only.
Fourth ”Legs only.
Fifth ”Spiracles only.
Sixth ”Spiracles only.
Seventh ”Spiracles, and sometimes claspers.
Eighth ”Spiracles, and sometimes claspers.
Ninth ”Spiracles, and sometimes claspers.
Tenth ”Spiracles, and generally claspers.
Eleventh ”Spiracles only.
Twelfth ”Spiracles only.
Thirteenth ”Claspers only, and these occasionally absent.

[Pg 36]

We must now watch the caterpillar through its later days, to
see how it prepares for passing into the pupal stage, and to
witness the various interesting changes that take place at this
period.

When fully grown, it ceases to eat, and begins to wander about
in search of a convenient spot for the coming event. Its colours
fade, and the body becomes appreciably smaller, especially in length,
as it ejects the whole contents of its digestive apparatus. According
to some accounts, it even evacuates the lining of the intestines
with their contents.

A great variety of situations are chosen by the different species
at this time. Some will fix themselves on their own food plant,
and there remain till they finally emerge in the perfect state,
suspending themselves from a silken carpet, hiding themselves
in a rolled leaf, or constructing a cocoon of some kind. A large
number walk down the food plants, and undergo their changes
in moss that happens to lie at the foot; or construct a cocoon
on the surface of the ground, utilising for the purpose any decayed
leaves, fragments of vegetable matter, or pieces of earth or small
stones. Many seek a further protection than this, and burrow
into the soil, where they either lie in a little oval cell that they prepare,
or in a cocoon constructed by spinning together some particles
of earth. Again, there are those caterpillars, chiefly of butterflies
that frequent our gardens, which find their way to the nearest wall
or fence, and there secure themselves in a sheltered nook. We
will watch a few of these varied methods of procedure, taking as
our first instance the caterpillar of the common Large White or
Cabbage Butterfly.

When fully fed, this larva seeks out a sheltered spot, generally
selecting the under surface of some object, or of the ledge of a
wall or fence. Sometimes it will not even leave its food plant,
though it generally walks some considerable distance before a suitable
shelter is found. Having satisfied itself as to the site of the
temporary abode, it sets to work at spinning a silken carpet. At
first the threads spread over a rather wide area, and seem to be
laid in a somewhat irregular and aimless manner; but after a little
time its labours are concentrated on one small spot, where it spins
several layers of silk fibres.

This done, it fixes the little hooks of the claspers firmly in its
carpet bed, and then proceeds with a highly interesting movement.
It is not satisfied with only the one mode of suspension. In fact,[Pg 37]
this alone would hardly be safe, for when it casts its skin, as it is
shortly about to do, its claspers will all disappear; and although it
afterwards secures itself by the ‘tail,’ it would be dangling in such
a manner as to swing with every breeze—a very unsatisfactory
state of affairs, especially with those that pupate late in the summer
and remain in the pupal state throughout the winter storms.

Its next procedure, then, is to make a strong silk band round the
middle of its body, so as to keep it close to the surface against which
it rests. But how is this to be done? It bends its head round till
the spinning organ can be applied to a point close beside the middle
of its body. Here it fixes one end of a thread; and then, gradually
twisting its body, brings its head round to the other side, still keeping
it close to the same segment, and fastens the other end of the
thread exactly opposite the point at which it started.

The head is now brought back to its former position, thus
adding another thread to the band; and the process is repeated
several times, till at last the caterpillar is satisfied with the thickness
and strength of the cord formed.

Now it straightens out its body as if to rest from its labours;
but the work is not yet complete. Soon it exhibits much restlessness.
Its foremost segments are seen to shorten, and consequently
become thicker. Then the skin splits, and the last moult of the
caterpillar commences. The movements that follow are exactly
similar to those we have already described in connection with one
of the earlier moults: the alternate and successive contractions of
all the segments gradually force back the old coat, and this is
finally thrown entirely off by a somewhat vigorous wriggling of the
‘tail.’

Then, for a moment, the creature is supported only by its silken
cord. But this lasts only for a moment. For, as soon as it is
quite free from the old garment, it applies its tail to the densest
part of the carpet it had prepared at the start, and secures its hinder
extremity by means of little hooks.

But what a change has now come over the creature! It is no
longer a caterpillar. Its head is no longer distinct, although we
can readily make out the positions of the eyes. Its mouth and
jaws have quite disappeared, and the legs and claspers are apparently
gone. The three segments that bore the legs are no longer distinctly
separable, though in reality they still exist. The head and thorax
are peculiarly shaped; and, instead of being cylindrical, are angled
and ridged; but, beneath the soft greenish skin—the new garment—we[Pg 38]
can discern the outline of a pair of small wings, and see a
proboscis and a pair of long antennæ. Also the six long legs of the
future butterfly can be traced with care.

The abdomen is conical in form, coming to a sharp point at
the end, and its segments are quite distinct.

No stranger to the metamorphoses of insects would connect
the present form with that of a caterpillar; they are so very
unlike. And yet the time occupied in the whole change, from the
spinning of the carpet, does not occupy more than about thirty or
thirty-five hours.

The apparent suddenness of this change is really surprising, but
in reality the transformation is not nearly so sudden as it appears.
Dissection of a caterpillar a few days before the final moult is due
will show that the changes are already going on. In fact, a
simple removal of the skin will prove that the organs of the
future butterfly are developing. Still, in proportion to the short
time occupied, the change is extremely great; and it may reasonably
be inquired, Why so great a change within so short a space of
time?—why is not the change continued steadily and equally
through the larval existence? The reason has already been hinted
at. Caterpillars are living eating machines, whose office is to
remove excess of vegetable matter. Consequently they must have
their jaws and bulky digestive apparatus in full development to the
end. If these organs were to gradually disappear as the caterpillar
reaches its non-eating stages, it would simply be starved to death.
So the change from the larval to the pupal state, which we may
regard as the final moult of the caterpillar, is a far greater change
than any of the preceding ones, and occupies a proportionately
longer time, although it is principally confined to the last few days
of the caterpillar life.

A number of caterpillars, and especially those of the butterflies,
suspend themselves when about to change; and the peculiarities of
the modes adopted must be left for our descriptions of species in a
future chapter; but we will find room here for one more interesting
example, taking this time the larva of one of the commonest of the
Vanessas (page 166)—the Small Tortoiseshell Butterfly.

The caterpillars of this insect are gregarious when young; and
if ever you meet with one, you are almost sure to be able to obtain
a hundred or so without much searching. But as they grow older
they feed singly, yet generally without straying very far from their
birthplace.[Pg 39]

When full grown they sometimes stray to a neighbouring plant
or fence to undergo the change to a chrysalis, but more commonly
they are perfectly satisfied with the protection afforded by the leaves
of their food plant. We will now watch one of these as we did the
larva of the Large White Butterfly.

Of course the under side of the leaf is chosen. Here a silken
carpet is spun as before described; but the caterpillar, instead of
clinging with all its claspers, suspends itself in a vertical position
by its hindermost pair only.

Here it hangs, head downwards, awaiting the coming events.
The splitting and casting of the skin goes on just as in the case of
the Large White, but there is this puzzle to be solved: how
can the insect shuffle itself out of its old coat without falling to the
ground, leaving the cast-off garments still hanging by the hooks
of the claspers? This really seems a matter of impossibility, since
the little hooks which alone suspend the insect are thrown off with
the skin of the claspers.

The thing is managed in this way. As the skin slowly splits
through the wrigglings of the apparently uncomfortable occupant,
it is gradually pushed backward—that is, upward—till it is in a
shrivelled condition, and the body of the insect is nearly free. But
the chrysalis thus brought to light is provided with little hooks on
the end of its ‘tail’ by which it can attach itself to the irregularities
of the crumpled coat. Its conical abdomen is also very flexible,
and it can, by bending this, seize hold of a ridge in the skin,
holding it between the segments. Thus, although practically quite
free from the old garb, it never falls to the ground.

There is now, however, another point to be attended to. The
newly formed chrysalis desires to be entirely independent of its
cast-off skin, and to suspend itself directly from the silky carpet it
has prepared. To this end it works steadily for a time, alternately
bending its supple abdomen from side to side, gripping the folds of
the skin between the segments, pulling its body a little higher at
each movement, and securing itself at each step by the little hooks
at its extremity.

So it climbs, and at last it reaches the network of silk fibres, and
thrusts the tip of its abdomen among them till some of the hooks
have taken hold. Not satisfied with this, it turns its body round
and round to get the little hooks so entangled between the silk
fibres that a fall is impossible, and in so doing it frequently pushes
the old skin out of its place so that it falls to the ground.[Pg 40]

Although the caterpillars of this species do not show any great
gregarious tendency when nearly full fed, yet it is not an uncommon
thing to find several hanging from the under surface of
one leaf, all being attached to the one common carpet at which all
had worked. And when bred in confinement, a number will often
spin in company in a corner of their cage. I have thus obtained a
cluster of thirty-seven pupæ, all hanging by the ‘tails’ to the
same mass of silk, which was so small that they formed quite a
compact mass of beings with their tails close
together.



Fig. 28.—The Cocoon of the
Emperor Moth.

Fig. 29.—The Cocoon
of the Six-spotted
Burnet (Filipendulæ).

We have seen that the Large White Butterfly
makes itself secure by a silk band round its
middle, while the ‘Tortoiseshell’ is fixed only
by its tail. But the extra provision for the safety
of the former is not so necessary in the case of
the latter, as it never spends more than two or
three weeks in the pupal state. Here it is the perfect insect that
braves the winter, and not the chrysalis.

There is a great variety in the means taken by the caterpillars
of moths to protect themselves during their metamorphoses, but we
shall have space for only a few illustrations.

A clever cocoon is spun by the larva of the Emperor Moth
(Pavonia). It is pear-shaped, and composed of a brownish silk;
and is so constructed that the newly emerged moth can easily walk
out of the small end without breaking a fibre, while the entry of an
insect enemy from without is impossible.

This is managed as follows. A number of rather stiff threads
are made to project from the small end of the cocoon, and these
converge as they pass outward so that the ends are all near[Pg 41]
together. The other portions of the cocoon are of compact silk,
and any insect intruder that ventures to enter by what we may
almost term the open end is met by a number of spikes, as it were,
that play on it at every attempt. Many of these wonderful cocoons
may be found during the winter months attached to the food plants
of this insect.

Of the silken cocoons spun by various caterpillars some are so
thin and light that the chrysalis can easily be seen through them,
and others are so densely woven as to be quite opaque. A
great difference is also to be observed in the adhesive power of the
silk fibres. In some cases little threads of silk can be pulled off
the cocoon; but some of them, that of the Oak Eggar (page 229) for
example, look as if they had been constructed of paper rather than
of silk, because, at the time of spinning, the moist silk fibres stuck
so closely together.

An extreme case of this character is to be met with in the
cocoon of the Puss Moth (page 235); for here the fluid from the
spinneret of the caterpillar does not harden at once on exposure to
air, and so the threads become thoroughly united together, thus
forming a solid gluey cocoon.

When the Puss caterpillar is about to change, it descends the
tree (poplar, willow, or sallow) till it is within a few feet of the
ground. Then it commences gnawing away at the bark, at the
same time cementing all the pieces together with the gluey substance
from its spinning glands. In this way it surrounds itself
with a very hard cocoon, which so closely resembles the surrounding
bark in colour that detection is difficult indeed.

But how will the caterpillar proceed if it is removed from its
native tree and has no bark to gnaw? That you can easily answer
for yourself, or rather Puss will answer it for you. Go and search
among the poplars, willows and sallows in the month of July. You
may possibly come across a caterpillar that is just in the act of
creeping down the bark in search of a resting place; but if not you
may be successful in obtaining a few either by examining the twigs,
or you may start them from their hiding places by smartly tapping
the smaller branches with a strong stick.

Having secured one or more larvæ, take them home, and they
will give some rather novel performances. If they are not fully
grown, you must supply them with fresh leaves every day till they
refuse to eat; and then is the time for your experiments. Shut one
in a little wooden box, and you will have the pleasure of watching it[Pg 42]
construct a cocoon of chips of wood that it has bitten out with its
powerful jaws, all joined together into a hard shell by means of
transparent glue. Shut another Puss in a glass vessel—a tumbler,
for instance—either by placing it under the inverted vessel, or by
covering over the top. Perhaps it will not be superfluous to mention
that, should you place it under an inverted vessel, this vessel
should not stand on a polished table, for, whatever be the material,
unless extremely hard, it is sure to be utilised in the manufacture
of the cocoon.

Let us suppose, then, that the caterpillar is under an inverted
tumbler that stands on a plate or saucer. Now it is for you to
decide what material shall be used in the construction of the new
home. Give Puss some fine strips of brightly coloured ribbon,
and it will construct a very gaudy house by gluing them together.
Or, provide it with sawdust, pieces of rag, glass beads, sand, paper,
anything in fact; and the material will be ‘made up’ into a
cocoon more or less ornamental according to the nature of the supply.

But what if you give it nothing with which to work, and so
inclose it that nothing its jaws can pierce is within its reach?
For instance, shut it in with tumbler and saucer as before, inverting
the former on the latter, and give it no material whatever.
What will it do now? We will watch and see.

At first it is very restless, and walks round and round the edge
of the tumbler, evidently a little dissatisfied with the prospects.
Then, after a little while, the events of nature transpiring in their
fixed order regardless of trivial mishaps, the glutinous fluid begins
to flow from the creature’s spinning glands, and it moves about in
a somewhat aimless fashion, applying the transparent adhesive
matter both to tumbler and saucer.

It seems now to become a little more reconciled to its unnatural
surroundings; and, making the best of bad matters, keeps its
body in one place, and starts the construction of a ridge or barrier
all round itself. By the continued application of the creature’s
spinneret this barrier is made gradually thicker and higher, till at
last the overhanging sides meet and the caterpillar is inclosed in
its self-constructed prison. But the walls of this prison are so
transparent that every movement can be watched; and, after the
insect has spent a few days in completing the cocoon, we can see
it cast off its old skin, and appear in the new garb of a fine
greenish chrysalis.

Its soft green skin soon hardens and turns to a rich dark brown[Pg 43]
colour, and it settles down for a long rest lasting till the following
May or June.

When the whole operation of building is completed, lift up the
tumbler, and up will come the saucer too. The two are firmly
glued together by the substance secreted; and the power of this as
a cementing material will be well illustrated if you endeavour by
mere pulling force to separate the two articles.

The Puss is not the only caterpillar that works up a foreign
material with the contents of the spinning organs. There are
several others, in fact, that use for this purpose fragments of wood
or other parts of the food plants; and a still larger number bind
together leaves, fresh or dead, or particles of earth or other matter.
Several such cocoons will be described in our accounts of
individual species in another chapter. We shall now devote a
little space to a few general remarks on the chrysalides and the
final metamorphosis of butterflies and moths.


[Pg 44]

CHAPTER IV

THE PUPA OR CHRYSALIS

As soon as the last moult of the caterpillar is over, the chrysalis
that had already been developing under the cover of the old skin
is exposed to full view; and although the perfect insect is not to
be liberated for some time to
come, yet some of its parts are
apparently fully formed.


Fig. 30.—The
Pupa of the
Privet Hawk
(Ligustri).

Fig. 31.—The
Chrysalis of
the Large
White Butterfly
(Brassicæ).

The newly exposed skin of
the chrysalis is very soft and
moist, but as it hardens it forms
a membranous or horny covering
that protects and holds
firmly in place the trunk and
the various limbs and appendages
that are distinctly to be
traced on the under surface.

If, however, you examine a
chrysalis directly after the moult
is over, you will often find that
the wings, antennæ, proboscis,
and legs of the future butterfly
can be easily separated from
the trunk of the body on which
they lie by means of a blunt needle, and can be spread out so as to
be quite free from that surface.

In form the chrysalides of butterflies and moths are as variable
as the caterpillars. Many of the former are sharply angular like
that of the ‘Small Tortoiseshell’ already mentioned; but some of
the butterflies—the Skippers (page 197)—have smooth and tapering
chrysalides, and so have most of the moths.[Pg 45]

In colour they are equally variable. Some are beautifully
tinted with delicate shades of green, some spotted on a light ground,
some striped with bands more or less gaudy and distinct, but
the prevailing tint, especially
among the moths, is a reddish
brown, often so deep that it is
almost a black.


Fig. 32.—The
Pupa of the
Dark Green
Fritillary (Aglaia).

Fig. 33.—The
Pupa of the
Black-veined
White Butterfly
(Cratægi).

As a rule there is no
marked resemblance between
the different stages of the
same insect. Thus, a brilliantly
coloured caterpillar
may change to a dull and
unattractive chrysalis, from
which may emerge a butterfly
or moth that partakes of the
colours of neither. But in a
few cases there are colours
or other features that remain
persistent throughout the three stages, or show themselves prominently
in two.

An interesting example in point is that of the Magpie or Currant
Moth (page 279). The caterpillar of this moth is cream-coloured,
with orange stripes along the sides, and very bold black markings
down the back. The chrysalis, which is at first entirely yellow,
afterwards turns black with the exception of some yellow transverse
bands. Then, the moth exhibits the same colours as these
two earlier stages, with the
same degree of boldness;
for its pale cream-coloured
wings, tinted with patches
of yellow, are marked with
numerous deep black spots.
Thus, in this case, we find
the same general character
of the colouring throughout
the insect’s existence.


Fig. 34.—The
Pupa of the
Currant Moth.

Fig. 35.—Pupa
of the Pale
Tussock Moth
(Pudibunda).

Another interesting example,
though not so striking as the last, is to be found in the case
of a group of moths known as the Liparidæ. The caterpillars of
these are remarkable for their very hairy bodies, often ornamented[Pg 46]
by several bold brush-like tufts. The chrysalides are also hairy;
and several of the moths themselves are not only thickly clad with
shaggy hair, but a bold tuft often tips the abdomen.

We must not leave these few remarks on the characters of
chrysalides without a mention of the brilliant spots of burnished
gold that decorate the pupæ of certain butterflies. This is the
feature that led to the invention of the term chrysalis, which is
derived from the Greek word chrysos, meaning gold. For the
same reason the term aurelia has been applied to the pupæ of
Lepidoptera, this being derived from aurum—the Latin name for
gold.

Strictly, then, these two terms apply only to the pupæ of a
certain number of the butterflies; but the former is now generally
used to designate the pupæ of all the Lepidoptera, and is even extended
to the corresponding stages of insects of other orders.

If you examine one of these gold-speckled chrysalides, the
brilliant metallic lustre seems to belong to the outer surface, just
as if certain spots had been tipped with real gold; but after the
butterfly has quitted its case the beautiful golden spots are gone.
This proves that the metallic appearance is not due to reflection
from the outer surface of the chrysalis, but to a reflection from some
structure beneath it. This latter is a very thin membrane which
lies just under the outer transparent covering of the chrysalis.

The period during which the Lepidoptera remain in the chrysalis
state varies very considerably in different species, and also
depends more or less on the temperature. As a rule, when a caterpillar
pupates before the end of the summer, it remains dormant
in the pupal condition for only a few weeks; but, if late in the
summer or in the autumn, it remains in this condition throughout
the winter, and emerges in the following spring or early summer.

Both these conditions are illustrated in the life history of the
Large White or Cabbage Butterfly—an insect with which we have
already become acquainted. We get two distinct broods of this
butterfly every year, the first appearing in May and the second in
August. The eggs of the first brood hatch in about a fortnight, and
the larvæ are full grown about four weeks later. These then change
to chrysalides, from which the perfect insects (the second brood)
emerge in a few weeks—the period varying slightly with the temperature
of the season. From the eggs of this second brood we
get another invading army of cabbage eaters that change to pupæ
late in the summer. These remain dormant till the following[Pg 47]
April, and may be found in numbers throughout the winter, attached
to the walls and fences of kitchen and market gardens.

If, then, the pupæ of the same species are so influenced by the
temperatures of the seasons, can we limit or prolong the period
of quiescence by subjecting them to high or low temperatures
artificially produced? Most certainly we can; and every practical
entomologist knows how to obtain the perfect butterflies and
moths of certain species long before their appointed times, or,
if he desires it, to compel them to remain in their dormant stage
long after the natural period has terminated.

Sometimes an enthusiastic insect hunter obtains a large number
of what we may term ‘winter pupæ,’ by collecting and breeding
various species. He also anticipates a number of successful captures
of perfect insects during the following summer. Thus, from two
distinct sources, he obtains a goodly assortment of butterflies and
moths, the setting, preserving, and arranging of which entails an
immense amount of home work.

Under such circumstances he will sometimes endeavour to cause
some of his pupæ to emerge before their accustomed time, so that he
may get some of his insects ‘on the boards’ before his field work
is in full swing, and so avoid a rush, or prevent the loss of insects
that will be spoiled before he has time to take them in hand.

This process of hurrying up his pupæ he calls ‘forcing,’ and
simply consists in keeping them for a time in a warm room or hothouse
where the high temperature is pretty constant.

On the other hand, the entomologist may desire to try the effect
of a continued low temperature on his pupæ. This he can do by
placing his pupæ in an ice house. Such experiments have often
been performed, and the results are very interesting. In some
cases the emergence of the perfect insect has been delayed for many
months, and even years; and then, after an exposure to a normal
temperature lasting only a week or two, the winged insect has
made its appearance just as if nothing unusual had happened.

Such are the effects of extreme temperatures on the duration
of the chrysalis state; and we naturally infer, from such results,
that the pupa under natural conditions is influenced, though in a
lesser degree, by the variations experienced with the seasons,
especially in such a fickle climate as our own.

The insect hunter has always to bear this in mind, and particularly
so when he sets out on a search for certain desired species.
Suppose, for example, he has set his mind on the capture of a[Pg 48]
certain butterfly that usually appears in the first week in May.
Before finally naming the day, he has to consider what the weather
has been during the last few weeks, and if he finds that this has
been much warmer than the average for the corresponding periods
in the past, he selects a day in April, earlier or later according to
the difference between the present season and the average.

If he does not pay due attention to such considerations, he will
sometimes find that all the insects netted are shabby and much
worn, even though, under average conditions, he would be catching
newly emerged and brilliant specimens. This, then, will explain
how it is that we so often see in entomologists’ periodicals startling
accounts of ‘early captures,’ and of the appearance of certain insects
late in the season that ought not to have emerged till the following
summer.

I will give just one illustration of these variations. The beautiful
Orange Tip Butterfly (Plate I, fig. 7) generally appears about the
middle of May in the southern counties. Farther north it is of
course a little later. In the north of England it has been taken in
June; and in Scotland as late as July. On the other hand, I have
taken it in Gloucestershire as early as March, on a rather bleak
day with a cold east wind; and, withal, in a field on the slope of the
Cotswolds fully exposed to the unfavourable breeze; but it was
evident that, in this case, the butterfly had been enticed from
its winter quarters by the milder weather of the few previous
weeks.

It may be as well, in passing, to observe that it is not only the
pupa that is influenced by temperature. The hatching of eggs may
be forced by high temperatures, or be retarded by exposure to cold;
and in nature the period of incubation varies with the seasons.
The larvæ, too, grow faster or more slowly, or pupate earlier or
later from similar causes. And so no very definite date or period
can be assigned to any one stage of any insect.

Now let us return to one of the chrysalides that we have already
watched through the earlier stages of its existence, and follow it in
its future development.

It is now, as we say, in its quiescent or dormant condition, but
we must not suppose that it is always in a profound sleep, nor can
we say that it is insensible to its surroundings. Touch it gently or
surprise it with a puff of air from your mouth, and it will begin to
wag its pointed tail, sometimes with such vigour as to send the
body rolling round and round in its box. Lay it on a bed of cocoa-nut[Pg 49]
fibre or finely sifted soil and let it remain quite undisturbed for
a few hours or days, and you will probably find that, by occasional
movements of its body, it has made a slight depression in its bed,
and lies partly submerged. I have known some chrysalides to
completely bury themselves in this way during the course of a day
or two, and others to partly expose themselves after having been
lightly covered. Others again, I have observed, will move smartly
if a strong light is suddenly turned on them. Many, too, certainly
appear to have a strong objection to exposure to the direct rays
of a hot sun; for, when thus exposed, they will struggle persistently,
as if to work their bodies into some shady corner. I
would not advise a young entomologist to try this experiment,
however, if he values the pupæ he possesses, for direct sunlight
is undoubtedly very harmful to many species, and perhaps it is
to all.

Some chrysalides are not nearly so active as has just been
represented; in fact, there are many which seem to show no signs
of life during the greater part of the time spent in that state. But
in all, whether apparently active or not, certain important internal
changes are at work. We have already noticed that, even in the
last days of the larval existence, some of the organs of the future
imago are to be traced. But these are as yet imperfectly developed.
We have also observed that a continuation of these changes,
gradually carried on, would be impossible in a voracious feeder; so
the insect, now fully grown, and no longer requiring a supply of
food, settles down in perfect quiet, submitting itself quite passively
to any further changes that nature may demand.

It has already suffered the loss of its claspers. Its wonderful
jaws that did so much damage (for good or evil as the case may be)
to the vegetable world are now gone, and the bulky digestive
apparatus has rapidly dwindled to useless dimensions. These and
other changes, already in progress, have to be perfected while the
creature is in a restful and helpless condition, though they may
often be retarded or even suspended during cold weather when
progress would certainly bring it to an untimely end.

But now the grandest of all these transformation scenes is
nigh at hand. The protective skin is already loosening from the
almost perfect imago, and consequently feels softer and far more
yielding than it did when in close contact with the body: the
swaddled butterfly or moth (for such the pupa is) is slowly preparing
to throw off its imprisoning garb. The wings and large[Pg 50]
compound eyes are assuming their final colours, which now begin
to show themselves through the more or less transparent skin,
and the long legs, the perfectly formed antennæ, and the slender
proboscis, all of which are folded closely under the creature’s thorax,
now begin to move within their loosened sheaths.

Now let us watch it closely, for one of the most wonderful sights
ever witnessed by a naturalist is about to be presented to our view.
We think we can observe slight movements; and, it may be, we can
actually see the struggling insect endeavouring to set itself free. The
legs and proboscis are moving within the loosened skin; and lo! as
we watch these motions, the prison wall bursts with a slight snapping
noise (at least, such is the case with some of the larger species),
and in a moment out pop a few long legs which immediately
struggle for a foothold. The proboscis also appears, alternately
lengthening itself out and coiling into a spiral, as if impatient to
reach the sweet nectar from the bottom of
some fragrant flower cup.


Fig. 36—A Butterfly,
just after
Emerging.

All this takes place in less time than one
requires to describe it; and, before many
seconds have passed, the struggling insect
has quite completed its last moult, and is
bidding good-bye to the rent garment that
has done it good service for so long a time.

But how dreadfully disappointing! Did
we not say only a few minutes since, that a
beautiful butterfly or moth was about to emerge? How, then, is
this? Here is an odd-looking creature, such as we have never seen
before! True, it has the right kind of body, though even that is so
soft and heavy that it is fairly dragged along as the insect walks.
Its antennæ, too, seem to be just the right thing—that is, just
what we were expecting to see. But oh! the wings! Are we
looking at a deformity?—a failure on the part of Nature to produce
what she ought?

We will not judge hastily, but continue to watch it a little
longer. It seems very restless at first, and, with the fluttering
apologies for wings, drags its heavy body along till it reaches some
surface up which it can climb. If nothing of the kind is close at
hand you may place a rough upright stick in its path, and it
will immediately begin to ascend. Its motto is now ‘Excelsior!’
and its ambition to rise may be so great that, on reaching the very
top of the stick provided for it, it struggles for a still higher position[Pg 51]
in life till, failing to get a foothold in the air itself, it falls to the
ground and has to retrace its steps.

I once thought I would like to test the perseverance of a large
moth in performing its first upward journey; and as it was one
from a chrysalis to be found in nature at the foot of a tree that
attains some considerable height, I was, of course, prepared to
exercise a little patience myself.

As soon as the moth had emerged, I placed it at the bottom of
a window curtain that hung from about eight feet high to the
floor. In less than half a minute it had reached the top, and was
struggling hard to get still higher. I took it down, and again
placed it at the bottom. Up it went as fast as before; and this
was repeated nine times with exactly the same result. For the
tenth time I placed the persevering creature at the bottom of
the curtain; and, after it had walked about halfway up, it suddenly
stopped, apparently quite satisfied with having travelled a distance
of over seventy feet in an upward direction. Its six legs were
immediately arranged symmetrically in a business-like manner,
and there it settled quite still, as if it had some definite object in
stopping just exactly in that spot.

But we must now return to our own insect, which has by this
time settled itself in a similar manner on the stick we provided
for it. The peculiar organs which represent the wings, though so
very small, show distinctly, in miniature, the colour and pattern of
the fully developed wings of the species. An interesting change is
just now commencing. These wings are apparently growing larger,
but the development is very unequal, so that they become curled and
crumpled till they are even more unsightly than before. All seems
to be going amiss. But this lasts only for a short time. The
fluid from the body steadily rushes into the nervures, causing the
wings to expand, and in a few minutes the beautiful pinions are
stretched to the full extent, assume their normal shape, and expose
the full glory of their brilliant colours.

It may be interesting if I give an example showing the exact
time taken for the full development of the wings of a certain
insect. So I will here quote an entry from my note book; and, by
the way, let me strongly advise all my young readers who follow
up this subject to habitually enter in a book kept specially for the
purpose all facts which strike them as they pursue their study of
nature. The note to which I refer runs as follows:

‘Early on the evening of the 22nd [April] I selected a few[Pg 52]
chrysalides of Populi [the Poplar Hawk Moth, page 209] which,
from the looseness of their cases, were thought to be just on the
point of emerging. At 8.46 one of them showed signs of restlessness;
and, after a few vigorous movements, during which it rolled
itself over on the glass [I had placed the pupæ on a piece of plate
glass so that slight movements might be more easily detected], the
front of its case was suddenly thrust off with considerable force;
and in less than four seconds the imago was quite free and
crawling on the table. After trying hard to reach a higher point
than was provided for about four minutes, it rested to expand its
wings—now about seven-sixteenths of an inch long, or one-third
the total length of the body. At 9 o’clock the wings reached
half the length of the body, and were much curled. At 9.12 they
were fully expanded and straightened out.’

From this extract we see that the whole period from the
bursting of the case to the full expansion of the wings was only
twenty-six minutes; and it will be well to remind the reader that
the process occupies even a much shorter time than this with
many species, both of butterflies and moths. It will be observed,
also, that the evening was chosen as the time for the observation.
There was a reason for this. The Poplar Hawk Moth, as is the case
with many others, almost invariably emerges from the chrysalis in
the evening—usually after dark. But it may be mentioned in
passing that a far larger number of the Lepidoptera as invariably
emerge in the morning.

Again we will return to our newly emerged insect, for there are
still one or two interesting points to observe. The wings have
fully expanded, it is true, but how very limp they are! Take the
creature on the tip of your finger and hold it so that its body is
in a horizontal position. Immediately the wings bend downward
with their own weight, so soft and flexible are they. The body, too,
is still very soft, and apparently much too heavy for flight. Then,
if you place it on a flat surface, it will immediately try to find
some perpendicular or overhanging surface from which it can
suspend itself by means of its legs, so that the pendant and
straightened wings are in the best possible position for drying. As
the insect walks away in search of such a resting place, the body
still drags as it did before, and the wings bend over, either both on
one side or one on each side of the body.

It is some time before the wings are sufficiently dry and rigid
for flight, but the period varies greatly with different species.[Pg 53]
Some of the small butterflies and moths take to flight long before
an hour has passed, but in many cases several hours elapse before
the creature starts from its first resting place. Butterflies that
emerge in the morning spend their first day actively on the wing;
but the nocturnal moths that emerge early in the day do not fly till
evening twilight. When, however, the time arrives, the insect
flutters its wings as if to test their power before committing itself
to the air; and frequently, after only a few seconds spent in this
preparatory exercise, off it darts with astonishing rapidity. But
others seem far more cautious. They vibrate their wings, sometimes
with such rapidity that they are lost in a kind of mist, and
with such power that their bodies would be carried suddenly into
the air were they not firmly anchored by three pairs of hooked
claws. Then, continuing the rapid vibration, they move slowly
along, always holding on firmly by one or more legs, as if to still
further satisfy themselves concerning the efficiency of their wings.
Then they venture on a few short trial trips from one neighbouring
object to another, and at last gain sufficient confidence for a long
voyage.

How strange must be the feelings of a winged insect during its
first flight! After a long period during which it was a helpless,
crawling grub, and this followed by a term of imprisonment during
which it was almost or quite shut off from the world, it now suddenly
acquires such great powers of locomotion that it is often a
match for ourselves.

But, alas! this life is short. A few days spent in sporting with
those it meets and in sucking the sweet juices of many flowers;
then a day or two during which the female deposits its eggs; again
a few days employed in pleasures that become less and less attractive,
till, at last, the creature becomes weary of life and settles
down to die.

We have now traced the complete life history of the Lepidoptera
from the egg to the perfect insect, avoiding descriptions that
apply only to certain species as far as possible, excepting where
such are useful as illustrations.

Only one thing more remains to be done before we start in real
earnest with our practical work. We shall shortly be giving hints
on the modes of capture, the ‘setting’ and the preservation of
butterflies and moths. And in so doing we shall often have to
observe important points in which our dealings with these two
great divisions of the order will differ very materially. Hence we[Pg 54]
must not consider ourselves ready to proceed with the practical
portion of the entomologist’s labours till we are perfectly satisfied
that we know the main features that enable us to distinguish
between the butterflies and the moths, and also know just a little
concerning the subdivisions on each side.

This, then, shall form the subject of the next short chapter.


[Pg 55]

CHAPTER V

CLASSIFICATION OF THE LEPIDOPTERA

The Lepidoptera are divided into two very unequal groups, to
which we have so frequently alluded as ‘Butterflies’ and ‘Moths.’
And, although these two terms are popularly applied in a fairly
accurate manner, yet, strange to say, very few persons indeed have
any definite knowledge of the differences that entomologists recognise
between the two groups.

Every entomologist has his circle of sympathetic and, perhaps,
even admiring friends. Consequently, many a little package is
sent round to his abode ‘with great care,’ accompanied by a note
or a message concerning the fine ‘butterfly I have just caught, and
thought you would like to add to your collection.’

The ‘butterflies’ that so frequently reach us through these
channels nearly always turn out to be brightly coloured moths,
and this naturally gives one the idea that the popular notion as to
the classification of the Lepidoptera is based on colour or brilliancy
of design, the term ‘butterfly’ being applied to the gayer species,
and ‘moth’ to the more dingy members of the race.

There is really some shadow of a reason in this method of
nomenclature, for butterflies are usually more brightly clad than
moths; but the scientific classification, at least as far as the main
divisions and subdivisions are concerned, has nothing whatever to
do with colour or design; and we must at once acquaint ourselves
with the fact that there are very dingy butterflies, and most
beautiful and highly coloured moths.

How shall we account for the fact that the specimens so kindly
sent us by our friends are generally moths? Is it because moths
are more numerous and more frequently seen? They are certainly
more numerous; for, while our butterflies do not number seventy[Pg 56]
species, the other division contains about two thousand. Yet, in
spite of this fact, moths are not generally observed as much as
butterflies, for the former are nearly all night-fliers, and the latter
always fly by day and rest by night.

Still our question remains unanswered. The reason is this.
The captives sent us are seldom caught on the wing. Most of our
grown-up friends, even though they admire our own pluck and
general carelessness concerning the remarks of the spectators of
our entomological antics, would not themselves like to be seen, hat
in hand, chasing a butterfly; and the night-flying moths are, of
course, less frequently observed. But they often, in the course of
their daily employments, meet with a large moth fast asleep
in some corner of a dwelling house, workshop, or outhouse. Such
moths are easily caught while in the midst of their slumbers,
and, as they often make no attempt to fly by day, are as easily
transferred to a box suitable for transmission by messenger or by
post.

In the above few remarks we have alluded to some features by
which the two great groups of the Lepidoptera may be distinguished;
but we have already referred (page 5) to a far more
important one in our description of the various forms of antennæ.
All butterflies—at least all British butterflies—have knobbed or
clubbed antennæ, while the corresponding organs of all our moths
terminate in a sharp point.

This distinction obtains in all British Lepidoptera, and is so far
regarded as the most important basis of classification that naturalists
have derived from it the two Greek terms that are synonymous
with our two popular names—butterflies and moths. The scientific
name for the former group is Rhopalocera—a term derived from
two Greek words, one signifying a horn, and the other a club, and
thus meaning ‘club-horned.’ The corresponding name for moths
is Heterocera, derived from the same source, and meaning ‘variously
horned.’

But, although we find embodied in these two long and formidable
names an unerring mark of distinction between British
butterflies and moths, we must not neglect other less important
facts which, though less distinctive, are not without interest.

Observe a butterfly at rest. Its wings are turned vertically
over its back, and brought so closely together that they often
touch. In this position the ‘upper’ surfaces of the ‘upper’ wings
are completely hidden from view, and the ‘under’ surfaces are[Pg 57]
exposed on the two sides, except that those of the ‘upper’ pair are
partly hidden by the other pair.

Now look at a moth under the same circumstances, and you
will generally find the wings lying over its body, which is almost or
completely hidden beneath them. As a rule the upper pair together
form a triangular figure, and entirely cover the second pair; but
in some cases a portion of each of the under wings extends beyond
the margin of those above them, and in others the upper pair
extend so far forward that nearly the whole of the under wings is
exposed behind them.


Fig. 37.—A Butterfly at Rest
(Large Copper).

Fig. 38.—A Moth at Rest
(Gothic).

Again, the wings of butterflies are so rigid that they can never
be folded; but you will observe that the under wings of moths are
generally very thin, soft, and pliant,
and are neatly pleated lengthwise when
not in use.

Another feature deserving notice is
a slight difference to be often observed in the form of the body.
The butterfly, which generally has a slender body, has a distinct
constriction or waist between the thorax and abdomen. This is
not so apparent with moths, and especially with the thick-bodied
species.

The Rhopalocera or Butterflies are divided into Families, each
of which contains insects that possess certain features in common
by which they may all be distinguished from the members of any
other family.

The British species represent eight families. They are as
follows:

1. Papilionidæ.—Containing only one British species—the
beautiful Swallow-tail (Plate I, fig. 1).[Pg 58]

2. Pieridæ.—Containing ten species. These are often known
collectively as the ‘Whites,’ but include four butterflies that are
distinguished by beautiful shades of yellow and orange.

3. Nymphalidæ.—This family contains seventeen insects,
among them being several splendid species. It includes the
Fritillaries and Vanessas.

4. Apaturidæ.—Of this we have only one representative—the
Purple Emperor (Plate V, fig. 1).

5. Satyridæ.—Including the ‘Browns’ and ‘Heaths,’ and
numbering eleven species.

6. Lycænidæ.—Including the Hairstreaks, ‘Coppers,’ and
‘Blues,’ in all seventeen species.

7. Erycinidæ.—Containing only the ‘Duke of Burgundy.’

8. Hesperiidæ.—This family contains seven British butterflies
commonly known as the ‘Skippers.’

Although all the members of the same family resemble each other
in certain points of structure, or in their habits, yet we can often find
among them a smaller group differing from all the others in one or
two minor particulars. Such smaller groups are called Genera.

To make this all quite clear we will take an example.

The Brimstone Butterfly (Plate II, fig. 4) belongs to the second
family—Pieridæ, all the members of which are distinguished
from those of the other families by the characteristics mentioned
on page 141.

But our Brimstone Butterfly possesses another very prominent
feature in which it differs from all the other British Pieridæ, and
that is the conspicuous projecting angles of both fore and hind
wings. Among the foreign species of the family we are considering
there are several that possess these angles; but as there are no
others among our own members, the ‘Brimstone’ is placed by
itself in the list of British Lepidoptera as the only member of the
genus Gonopteryx or ‘angle-winged’ butterflies.

Thus the full relationship of this butterfly to other insects may
be shown in the following manner:

The Brimstone Butterfly.

  • ORDER.Lepidoptera
  • Section.Rhopalocera
  • Family.Pieridæ
  • Genus.Gonopteryx
  • Species.—Rhamni

[Pg 59]

Now, every butterfly has a Latin or Greek name in addition to
that by which it is popularly known. I should have said two Latin
or Greek names. The first of these is always the generic name,
and the second is the one by which we denote the particular
member or species of that genus. Thus, the scientific name of the
Brimstone Butterfly is Gonopteryx Rhamni.

‘But,’ the reader may be inclined to ask, ‘why should we not
be satisfied with the one popular name only?’ And, ‘If we must
have a separate scientific name, could we not find suitable terms
among our English words to build up such a name—one that
might express the principal characteristics of the insect, and also
serve all the purposes of classification?’

Such questions sound very reasonable, and so they are. But
the entomologist’s answer is this. We ourselves may get on well
without the help of the dead languages, but we have brother
naturalists all over the world, speaking a great variety of different
languages. We endeavour to help one another—to exchange notes
and generally to assist one another in our labours; and this can be
greatly facilitated if we all adopt the same system of nomenclature.
The educated of most of the great nations generally know something
of Latin and Greek, and consequently the adoption of these
languages is generally acceptable to all.

This sounds well, but for my own part I believe that if we are
to make any branch of natural history a popular study, especially
with the young, we must to a certain extent avoid anything that
may prove distasteful. There is no doubt whatever that many a
youngster has been turned away from the pursuit of the study of
nature by the formidable array of almost unpronounceable names
that stretch nearly halfway across a page; and those who desire
to make such a study pleasant to beginners should be very cautious
with the use of these necessary evils. One would think, on glancing
over some of the scientific manuals that are written ‘especially
for the young,’ that the authors considered our own too mean a
language for so exalted a purpose, for in such works we find all or
nearly all the popular names by which the schoolboy knows certain
creatures he has seen entirely omitted, and the description of a
species appended to a long Latin term that conveys no idea whatever
to the reader, who is studying the description of a well-known
animal or plant and doesn’t know it.

Our plan will be to give the popular names throughout, except
in the case of those few species that are not so well known as to[Pg 60]
have received one; but the scientific names will always be given
as well for the benefit of those readers who would like to know
them. And the short description of the method of classification
just given will enable the more ambitious of my readers to thoroughly
understand the table of British butterflies and moths
toward the end of the book.

This table includes all the British species of butterflies and of
the larger moths; and the arrangement is such as to show clearly
the divisions into sections, families, &c. It will therefore be of
great value for reference, and as a guide for the arrangement of
the specimens in the cabinet.

In the foregoing description of the method of classification
butterflies only are mentioned; but the division and arrangement
of moths is carried out in just the same manner except that the
system is a little more complicated. The number of moths is so
large in comparison, that we are able to select from them some
very large groups the species of which possess features in common.
These groups are termed tribes, and are again divided into families
just like the butterflies. Thus the arrangement of moths includes
tribes, families, genera and species. We will take an example by
way of illustration as we did before, and ask the reader to verify
the same by comparison with our table:

Example.—The ‘Common Tiger’ (Plate X, fig. 3).

  • ORDER.Lepidoptera
  • Section.Heterocera
  • TRIBE.—Bombyces
  • Family.Cheloniidæ
  • Genus.Arctia
  • Species.—Caia
  • Scientific Name.—Arctia Caia.

I have already said that the Latin and Greek names of butterflies
and moths are not at all necessary to the young entomologist.
It is quite possible to be well acquainted with the natural history
of these creatures, and to derive all the pleasure and benefits that
the study of them can afford without the knowledge of such names;
but most entomologists go in for them, often to the entire exclusion
of the popular English terms.

There are those who consider themselves (or would have us
consider them) expert entomologists because they have the power[Pg 61]
to vomit forth a long list of scientific names of butterflies and
moths which (to them) have no meaning whatever; and it is astonishing
that we meet with so many youngsters who can rattle
away such terms, and, at the same time, are totally ignorant of
the real nature of the creatures they name.

If you wish to be a naturalist in the true sense of the term, study
your specimens, and take but little pains to commit their hard
names to memory; and you will then find that the latter will
gradually become your own property without any special effort on
your part. Your continued reference to illustrated works and
museum collections will bring them to you almost unconsciously,
and you will generally find your entomological vocabulary extending
as rapidly as your cabinet becomes filled.

Again, with regard to the meanings of the scientific terms, don’t
trouble much about them. It unfortunately happens that in a very
large number of cases these names are ill chosen, and do not in any
way refer to the distinguishing characteristics of the species to
which they are applied. You will observe, too, if you look at the
table, that many insects have two scientific names applied to the
species, one being placed in brackets after the other. In such
cases both these names are in common use, having both been
applied by independent authorities, and the insertion of the
two will prove an assistance at times.

It is a common practice with entomologists, in their communications,
to use only the second or specific name of insects. Thus,
they would speak of the Brimstone Butterfly as Rhamni, and not
Gonopteryx Rhamni. When writing a communication, however,
they very commonly place in front of the specific name the initial
letter of the first or generic name. Thus the full title of the
butterfly just mentioned would be abbreviated to G. Rhamni.

Having said so much concerning the principles of classification
and nomenclature, we will pass on to the practical portion of the
entomologist’s work.[Pg 62]


[Pg 63]

PART II

WORK AT HOME AND IN THE FIELD


CHAPTER VI

CATCHING BUTTERFLIES AND MOTHS

It is not at all surprising that entomology should prove such a
fascinating study to the young, and more especially that portion
which deals with the department we are now considering. Butterflies
and moths are among the most beautiful and most interesting
of living creatures. The study of their life history is enchanting,
and the creatures themselves are of such a size as to be conveniently
handled and preserved, and withal occupy so little space
that anyone with only moderate accommodation may possess a
fairly typical collection.

Compare the work of the entomologist with that of one whose
hobby is the study of mammals. The latter has to deal with large
and cumbersome objects, a collection of which requires an enormous
amount of space; and, unless he has the time and means to
travel in foreign countries, he cannot get together a good typical
collection of specimens representing his particular branch, for the
few British mammals contain no representatives of several of the
orders into which the class is divided.

Entomology is undoubtedly, par excellence, the study for
youngsters. It is equally suited to the studious and to those of an
adventurous turn of mind. It leads its follower into the bright sunshine
and the flowery meadows; and with body and mind pleasantly
occupied, the joy of living is deeply felt. The necessary apparatus
can be made by anyone. No dangerous gun is required, and there
are no precipitous rocks to scale. When the autumn flowers fade
the year’s work of the entomologist is not done, for the arranging[Pg 64]
of his cabinet and the demands of his living specimens keep him
more or less actively engaged until the flowers of the following
spring call both him and the insects he loves once more into the
field. And so, season after season, and year after year, he finds
himself engrossed in labours so fascinating that idleness—the curse
of so many of our youths—is with him an impossibility.

I assume that the readers of this book have a desire to take up
the study of one branch of entomology—that of butterflies and
moths—in real earnest; that they intend not only to read about
these interesting insects, but to know them. And there is only one
way in which one may really get to know living creatures; that
is by searching them out in their haunts, observing their growth
and habits, and by an occasional close examination in order to
become acquainted with their structure.

Hence I shall in this, the practical portion of the work, give
such information as will assist the beginner in catching, preserving,
rearing, breeding, and arranging the specimens that are to form his
collection.

Catching Butterflies

There was a time when we would try to capture a butterfly at
rest on a flower by a quick sweep of the hand, or, more commonly,
by a sharp downward stroke of the cap. We were led to this action
by a mere childish love of sport, or by a desire to possess an insect
simply because it was pretty. When we succeeded in securing our
prize, we handled it somewhat carelessly, often passing it from one
hand to the other, or boxing it in our closed and perspiring fist till
our fingers were dusted with the pretty microscopic scales of the
creature’s wings, and the wings themselves, stripped of all their
beautiful clothing, were merely transparent and veined membranes.
Having thus carelessly but unintentionally deprived the creature of
its greatest beauty, we set it free, often in such a damaged or
exhausted condition that the poor thing could scarcely fly.

But our childish ideas and inclinations have vanished. Now
we would rather watch the insect than catch it, for we find much
pleasure and interest in its varied movements. And if for purposes
of study we occasionally require to make one captive, we proceed
in such a manner as to preserve its beauty unimpaired. The cap
now gives place to a well-made and suitable net; and we are
careful to provide ourselves with sufficient and proper accommodation
for our captives.[Pg 65]

It is probable that many of my readers are as yet unacquainted
with the nature of an entomologist’s requirements for field work,
so we shall describe them, confining ourselves at first to those that
are required for a butterfly hunt.

First and foremost comes the net. This essential portion of your
equipment may be either purchased or constructed by yourself.
Very little skill is required to enable you to do the former. Provided
your pocket is well charged, you may start off at once to the
dealer in naturalists’ appliances, and treat yourself to a complete
outfit. But even in this case a little advice may not be out of
place. See that what you purchase is very strongly made. You can
get nicely finished nets constructed on the most convenient principles,
made to fold and go in an ordinary coat pocket, but with
weak joints. See that you have the most convenient form of net
by all means, but do not
go in for convenience and
appearance at the expense
of strength and durability.
Nothing is more annoying
than to find your net give
way just when you are in
the midst of a good day’s
sport.


Fig. 39.—A Wire Frame
for a Butterfly Net.

Fig. 40.

The folding net is certainly
very convenient, for
you can conceal it in your
pocket while you are walking
through town or travelling in a railway carriage, and thus avoid
that contemptuous gaze which certain of the public are prone to
cast on a poor ‘bug hunter.’ And although such nets are generally
purchased, yet they may be constructed by anyone who has had
experience in the working of metals. But other forms of nets,
equally useful and even stronger, can be made by anybody; and I
will give a few hints on two or three different ways of putting
them together.

A very simple and strong frame for a net may be made as
follows: Get a piece of stout iron or brass wire about forty inches
in length, and bend it into a circle with the two ends, turned out
about two inches each, at right angles to the circumference as
shown in the accompanying sketch.

Now take a good tough stick, the length of an ordinary walking[Pg 66]
stick, and cut out two grooves opposite each other at the end, just
large enough to take the straight ends of the wire. The end of the
stick will now resemble fig. 40 in shape. Place the ends in their
grooves, and bind them tightly to the stick by a good many turns
of rather fine wire.

A frame well made after this fashion is as strong as anything
you could desire, but it has the disadvantage of being always fixed
to the handle, thus preventing the use of the latter as a walking
stick when you are not directly engaged in your entomological
work.

A much more convenient frame may be made by thrusting the
ends of a piece of cane into the two narrow arms of a metal Y.
You may purchase the Y at any of the naturalists’ stores, or you
can make one yourself if you know how to perform the operation of
soldering. I have always made mine with odds and ends of brass
tubing such as old gas pipes. One piece must be just the size to
fix on the stick; and the other two must fit the cane
tightly. The three pieces must be filed off at the
proper angles, and the doubly bevelled end of the
wider tube must then be flattened down to the
width of the smaller ones before soldering. If you
decide to buy one, give the preference to strong
brass rather than the cheaper and more fragile ones
made of tinned iron.


Fig. 41.
The Metal Y.

The advantage of such an arrangement over the
last frame is evident at once. The cane, with net attached, can
be pulled out of the Y when not in use, and bent small enough to
go in the pocket or a satchel; and the Y can also be separated
from the stick, thus allowing the latter to be used as a walking
stick.

Some entomologists speak very favourably of what is known
as the ‘umbrella net’—a large and light net that will shut up like
an umbrella, and may even be made to look very much like this
useful protector, but the possession of such an imitation is somewhat
tantalising in a pelting shower. The ring of this net consists
of two steel springs attached to a couple of brass hinges, one of
which is fixed near one end of the handle, while the other slides up
and down in the gamp fashion.

One other form of net—’the clap net’—although still occasionally
seen, has had its best days. Two sticks are provided to this
one, so that the two sides of the net may be brought together on[Pg 67]
the insect; but as both hands are required to manage it, it is almost
surprising that it ever had any advocates at all.

When your frame is completed, sew round it a strip of strong
calico, to which the net itself may be afterwards sewn, for the lighter
material of the net is too delicate to stand the constant friction
against the metal or cane frame.

The material usually employed in making the ‘bag’ is called
leno. It can be purchased at most of the drapers’ shops, and three
colours—white, yellow and green—are usually kept in stock.
Measure the circumference of your net frame, and see that you get
sufficient leno to make a good full net. Suppose, for instance, that
the circle of your frame measures thirty-six inches round, then your
leno should be at least forty inches in length. Fold this double,
and then cut out two pieces of the shape shown in fig. 42, letting
the depth of the net be nearly or quite equal to the width of the
material. There is nothing to be done now but to
stitch the bag together and sew it to the calico on
the ring.


Fig. 42.

At first you will find the leno rather stiff and
harsh, but a damping and good rubbing between
the hands will soften it down; or, if you prefer it,
you may soften the material by a slight washing
before cutting out the net. The latter is perhaps
the better plan, for the washing will remove the
objectionable ‘dressing’ that renders the material
rather hard and stiff.

Of the three colours mentioned above, green is the one most
generally chosen, because it is more in harmony with the surroundings
of a butterfly catcher; but many prefer the white leno
to the green, as the insects are more easily seen in a net of this
colour. Yellow is certainly not a desirable tint.

As a rule it will be necessary to kill an insect as soon as it is
captured. This is always the case with butterflies unless you
require to keep them alive either to watch their movements or to
obtain eggs. For this purpose you will require a killing bottle or
box containing some volatile substance.

The selection of this necessary piece of apparatus is a point
deserving of much consideration, for so many different forms are in
use by different entomologists, and so many advocates each declare
that his own plan is far superior to that of any of the others, that
the final decision is not to be worked out in a moment. The best[Pg 68]
thing for a beginner is to try as many as he can, and then, after
some considerable experience of his own, he will be able to decide
which apparatus suits himself best.

I recommend this because it is impossible to say of any one
plan that it is the best, for that which gives perfect satisfaction to
one individual will often fail to give anything but annoyance in
the hands of another.

To enable my young readers to follow the advice I have just
given, I will describe some of the commonly used killing arrangements
and show how they should be used.

I will take first the ‘cyanide bottle.’ This is a wide-mouthed
bottle, containing a very poisonous substance called cyanide of
potassium
. It is fitted with a good sound
cork. The ‘cyanide’ is a solid substance, and
must be fixed in some way or other at the
bottom of the bottle so that it cannot shake
about and damage the butterflies.


Fig. 43.—The Cyanide
Bottle.

A cyanide bottle can be purchased ready
for use at the cost of a shilling or thereabouts;
but if you are old enough to be trusted with
deadly poisons, you may buy the ‘cyanide’ of
a chemist who knows you well and is satisfied
as to your intentions, and then prepare your
own. Every entomologist should know how
to do this, for the poison loses its power after
some time, and it is not always convenient to
leave your bottle in the hands of a chemist or
a ‘naturalist’ to have it recharged. This will
cost you more than it would to do it yourself,
but that is nothing compared with the annoyance that may result
when, the night before an anticipated butterfly hunt, you are calmly
told that ‘your bottle will be ready in a few days.’ You can charge it
yourself in a few minutes if you can manage to keep a small supply
of ‘cyanide’ in stock, and it is ready for use very shortly after.

Here is the modus operandi.—Purchase an ounce or two of the
cyanide of potassium, and immediately put it into a stoppered or
well-corked bottle. Label it at once, not only with the name,
but also with the word Poison in very large and conspicuous
letters. This dangerous chemical is often sold in sticks that look
much like certain ‘sugar sticks’ I was acquainted with in my
younger days; but whether this is or is not the case with your[Pg 69]
cyanide, see that the bottle is kept quite out of the reach of the
inquisitive and sugar-loving juveniles of the house.

The quantity above mentioned is more than you will require for
the first ‘charge,’ but you will soon experience the convenience of
having a supply always at hand for recharging when your cyanide
bottle fails to do its work expeditiously, or when an accident calls
for the somewhat sudden appearance of a new one.

Now procure a bottle for your work. Its mouth must be wide
enough to take the largest insect you hope to catch, and the widest
part of the bottle need not be much larger. Get a perfectly sound
cork to fit it tightly; and, to insure the more perfect exclusion of
air, paint over the top of the cork with melted paraffin wax.

Dissolve a few drams of the cyanide in a little water, using a
glass rod to stir up the mixture till the solid has all disappeared;
and be careful that neither the solid nor the solution touches
the skin if it should be in the slightest degree scratched or
broken. Now sprinkle plaster of Paris into the solution, a little
at a time, and stir all the while. As soon as the mixture begins
to set, pour it into your bottle as cleanly as you can—that is, without
touching the sides—and press it down with the flat end of a
stick if it is not level. Now cork it, and put the bottle away in a
cool place till required for use.

This is, I think, the best way of charging the bottle; but there
are two other common methods that may, perhaps, be regarded as a
little more simple. One is this: put a few small lumps of the
‘cyanide’ into your bottle, and then cover them with a stiff mixture
of plaster of Paris and water, and press down as before. The other
plan is to cover the ‘cyanide’ with a few thicknesses of blotting
paper, cut just a little larger than the inside of the bottle. The first
of these two methods is fairly satisfactory, but I have always found
that the charge, when made in this way, has a tendency to become
wet and pasty, in which condition it will spoil the wings of the
insects. The other is very objectionable, especially for field work,
for the blotting paper fails to keep its place while you are on the
chase. If the plaster is used, the mixing must be done quickly and
without hesitation, or the mixture will become solid before you can
press it into your bottle.

We will not enter now into the pros and cons of the cyanide
bottle, but will consider the advantages and disadvantages of the
various methods of killing the insects after we have noticed a few
more.[Pg 70]

The ‘laurel box’ has had many devoted advocates, although it
does not seem to be much in use now. It is a very good arrangement,
however, but is a little more troublesome than the cyanide
bottle, as it requires frequent replenishing.

A very good laurel box may be prepared as follows. Get a
small tin box of cylindrical form, measuring about five inches by
two, and cut a circle of perforated zinc or wood just the size to
fit it snugly as a false bottom without any danger of falling out of
its place. Now gather some of the young leaves of the green laurel
bush, and beat them almost to a pulp with a mallet or hammer.
Place this in your tin box, and press down the perforated false
bottom on it. The bruised laurel leaves give off
a very powerful odour, which stupefies butterflies
immediately.


Fig. 44.—Section
of the Laurel
Box.

a, space for insects;
b, perforated partition;
c, bruised
laurel leaves.

Of course the reader may be able to think
of various other ways in which the laurel box
may be made. Any arrangement will do providing
the vapour can come to the insects without
allowing the leaves to touch their wings;
and any ingenious youth could manufacture a
more satisfactory article than the one I have
mentioned. My desire is, as far as possible, to
give instructions that may easily be carried out
by anyone, even if he has not the slightest
mechanical skill, leaving the clever youth, sometimes,
the opportunity of displaying his own inventive
power. But in this case I will give a
few suggestions concerning other ways in which
a laurel killer may be constructed. A firm and fixed false bottom
is a decided advantage. This is easily managed by fixing a circular
piece of perforated zinc or ‘tin’ by means of a little solder; or even
a wood partition may be used, fixed with a few brads, driven into
it from the outside. With the fixed partition, however, you must
have a lid at each end of the box. This is easily managed if you
get two tins of the same size, knock out the bottom of one, and fit
the lid of the other in its place.

I have heard of laurel boxes without any partition save a piece
of rag in which the bruised leaves are wrapped. The whole is
pressed into the box so firmly that it is not likely to be displaced
while you are on the chase. I do not recommend this, for in addition
to the chance of its slipping there is a danger of the sap of the[Pg 71]
leaves exuding through the rag and spoiling the insects’ wings.
But if the reader should prefer to try this on account of its simplicity,
it will probably occur to him that a bottle may be used instead
of a tin box.

A well-made laurel box, with a fixed metal partition, is a piece
of apparatus strongly to be recommended to all young entomologists
who desire to test the relative value of the various poisons
that are used by the different experts; for with it any one of these
substances can be used. In the poison compartment you can place
pieces of ‘cyanide’ wrapped in blotting paper, or any kind of
porous substance moistened with liquid ammonia, chloroform,
benzole, or any other volatile liquid insecticide. All the above-named
substances are declared to be ‘the best,’ so they must all
be worth the trial.

‘Cyanide’ is valued on account of its lasting powers. A cyanide
bottle well charged will retain its efficiency throughout a whole
season. I always recharge two in the spring, one for active service
in the field and the other as a reserve force; and these kept in a
cool place do good execution throughout the year. If they should
exhibit a slight failing, a few minutes’ warming before a fire will
improve them; but for field work it is better to recharge. At
the same time see that the corks are in good condition.

Next to the ‘cyanide,’ the bruised laurel takes the first rank for
permanency; but you must not expect this to last many days.
For a few days’ continuous work one charge will suffice, but if the
laurel box has not been in use for some time you must have a fresh
supply.

The liquid poisons, such as ammonia, chloroform, and benzole,
are so volatile that they are very powerful for a short time, but so
much vapour is lost each time the box is opened that it is absolutely
necessary to carry a bottle of the one you use into the field with
you. Also see that you have sufficient of the blotting paper or
other absorbent to prevent the liquid from leaking through the
perforations of the partition.

If you choose ammonia—a substance that is not regarded as a
poison, and is therefore easily obtained from any chemist—always
get the strongest, and see that it is labelled ‘Liq. Ammonia, S.G.
·880’ as a guarantee. A small bottle such as you can conveniently
carry in the waistcoat pocket will contain sufficient for a day’s
work. Use only a few drops at a time, but renew frequently.
Although the ammonia corrodes cork, yet a good cork is far preferable[Pg 72]
for the pocket to a glass stopper, for its elasticity prevents
it from losing its hold, and the liquid from saturating your pocket
and its surroundings; but a glass stopper is certainly better for the
stock solution kept at home.

Most of the above remarks apply equally well to benzole and to
chloroform, but the latter is so powerful a poison that a very little
is required for a day’s work, and consequently a very small
bottle is more convenient. The dealers in naturalist’s appliances
supply metal ‘chloroform bottles’ with screw stoppers and a small
nozzle that will allow the liquid to run out only in drops. This is
a very good arrangement, since it enables you to avoid the ‘drop
too much’ which is not only unnecessary and therefore wasteful,
but saves you from experiencing the disappointment
of an empty bottle before your work is half done.


Fig. 45.—The
Chloroform
Bottle.

Some entomologists recommend the solid carbonate
of ammonium instead of liquid ammonia, but this is
not so powerful. It must be remembered that we
have the butterflies to consider, as well as our own
convenience, in the selection of the poisons we use.
It is the opinion of many well-known entomologists
that ‘insects cannot feel pain,’ and that we are therefore
at liberty to deal with them in any way we please.
Still it is as well to save all possible suffering, and be
satisfied with no killing box that is not practically
instantaneous in its effects.

Among other poisons used by entomologists I may
mention sulphur fumes and tobacco smoke. The former may be
obtained by burning a little sulphur or a sulphured lucifer match
under the perforations of a killing box of the pattern described, and
the latter—well, every smoker knows that. I should at once condemn
the former method, at least for field work, as troublesome
and inconvenient; and as to the other, I have tried the effect of a
puff (and many puffs) of tobacco smoke on an imprisoned insect,
but was so dissatisfied with the result that I am not likely to do so
again.

We have now considered a good many insecticides more or less
suitable to our purpose, but there still remains the unsolved problem
as to which is the best. Each one has its advantages. For
convenience nothing beats the cyanide bottle. It is very speedy in
its action, and the use of a bottle is a little preferable to a metal
box, for you can always satisfy yourself as to its efficiency without[Pg 73]
opening it. Cyanide, chloroform, benzole, and some others render
the insects more or less brittle and stiff, so that it is not so easy to
‘set’ them for the cabinet. Perhaps, if you happen to have a
supply of growing laurel close at hand, you cannot do better than
stick to the laurel box. The time taken in bruising up a few leaves
is inconsiderable, and the moisture given off from them will keep
your insects moist and supple, or will even ‘relax’ them if they
have become rigid. But try various plans for yourself, and you
will be able to settle a question which all the entomologists in the
world cannot answer for you—which method answers best in your
hands.

The next item for our consideration is the ‘collecting box.’
This is merely a box in which the butterflies are pinned as soon as
they are dead. Here, again, we shall note a few variations from
which a selection can be made according to the means or the
ingenuity of the reader. For a couple of shillings you can obtain
a good zinc collecting box, lined with cork, of oval form (a most
convenient shape for the pocket), and quite large enough for one
day’s captures; and half that modest sum will purchase a wooden
box, also lined with cork, adapted to the same purpose.

As with many other things, so with collecting boxes, the cheapest
is often the dearest in the end. You may feel inclined to save a
shilling by buying a wooden box, but you are sure to discard it after
a little practical experience for a metal one. We shall speak a little
later on concerning the advisability of ‘setting’ the butterflies as
soon as possible after capture; but this is not always practicable,
especially after a good day’s catch. Now, if the insects are pinned
in a wooden box, they soon become dry and rigid, and consequently
cannot be ‘set’ till they have been put through the more or less
tedious process of ‘relaxing.’ If you use a wooden collecting box
you will often find, on a hot and dry day, that all or nearly all your
butterflies are rigid before you arrive home; but a metal box will
keep them moist and supple, so that you can even put off the
setting till the following day if you are unable to do it immediately
after your return.

Another point worth considering is the best economy of space. If
your collecting box is only about one inch deep inside, you have
room for only one layer of pinned insects; but a box only a little
deeper may be lined with cork both at top and bottom, and thus be
made to accommodate double the number. The zinc boxes sold by
the dealers are generally lined with cork in this manner, and are,[Pg 74]
of course, deep enough for the double layer of specimens; but the
wooden boxes are sometimes lined on the bottom only. After these
few remarks you will at once see the economy of expending the
extra shilling on the former.

Although the prices of collecting boxes are low, yet there are
many who would prefer making their own, and there is much to be
said in favour of this. A great deal of pleasure is to be derived
from the construction of your own apparatus, especially when that
apparatus is afterwards to be used in the pursuit of a delightful
hobby. During the whole of the time thus engaged, you are looking
forward with the most pleasurable feelings to the glorious treat
before you, and every joint you make seems to bring you nearer to
the realisation of your joys. During the bleak winter months there
is no better employment for an entomologist who has a little spare
time than the preparation for the next outing. It is just one of
those artful schemes by which he seeks to get as much pleasure out
of life as it is capable of affording. How many there are who,
for the lack of a pleasant and instructive hobby, find their leisure
hours the most dismal of all, and who complain of the toil and
wearisomeness of their lot! The mournful thought with them is,
‘Is life worth living?’ but who ever heard such an expression from
the lips of an active entomologist?

But I must have done with moralising and proceed to business.
The question is—How shall we set to work about the construction
of a collecting box? If it is to be a wooden one, select or make a
box of such a size as to suit your pocket or satchel, and cover the
bottom, and lid too if the depth allows of it, with sheet cork or
slices of good wine corks, about one-eighth of an inch thick, fixed
on with glue.

The metal box is not quite so easy, but even here you may
save yourself much work by keeping your eyes open. Very neat
little collecting boxes can be made out of the flat metal boxes in
which are sold certain favourite brands of tobacco. Some of these
are just the right depth, and also of a very convenient size for the
coat pocket. Beg one of these boxes from a smoking friend, and if
the lid is not held by a hinge (a great advantage, by the way), you
can easily solder on a brass one.

All that remains now is the fixing of the cork. Buy a sheet
of cork at a naturalist’s shop, this being a commodity always in
stock, and cut out two pieces just the size to cover the bottom
and the lid.[Pg 75]

Gum and glue are not very satisfactory as fixing agents, for, as
you will presently learn, there are times when it will be necessary
to keep the box moist, and moisture softens both these substances.
The cork must be fixed by means of little strips of metal. Here
are two ways of doing this:

First.—Cut a few little strips of sheet tin, each about two inches
long and one-eighth wide. Double and bend them as shown in
fig. 46, and solder them to the surfaces which the cork is to
cover (fig. 47). As the cork is pushed in its place, these little
slips are allowed to force themselves through slits in it made by
means of a penknife, and then the ends are bent over as shown in
fig. 48. Two or three such fasteners will be quite sufficient to hold
down each sheet of cork.



Fig. 46.


Fig. 47.


Fig. 48.


Fig. 49.

Second.—Put the sheets of cork in their places first, then
make a few little slits through both metal and cork with the
point of a penknife, and then bind the two together with a
few ordinary paper fasteners. This arrangement is shown in
section in fig. 49.

Just one point more concerning the metal collecting box. You
will often call moisture to your aid in keeping the butterflies
flexible and soft. This will have but little action on zinc, but will
sooner or later cause the ‘tin’ (really tinned iron) box to rust.
Here, then, is a point in favour of zinc, but still a home-made ‘tin’
collector will last a long time if kept dry when not in use.

As already hinted, there are times when it is desirable to take
home certain butterflies alive, either for a study of their movements
or for the purpose of securing eggs for breeding. To this end you
must provide yourself either with a number of ‘chip boxes’ with a
few small holes pricked in the cover, or with some metal boxes
with perforations for the admission of air. If the latter, you will[Pg 76]
have no difficulty in securing a few ‘tin’ boxes of suitable size,
but, as the surface of the metal is very smooth, you should always
introduce a few leaves or something else that will provide a foothold
for the inmates.

The last item of the outfit is the pins. Ordinary draper’s pins
are quite out of the question. They are far too thick and clumsy for
the collector’s work. If you are not already acquainted with the
‘entomological pins,’ you had better ask a dealer to give you a
sample card. This will be very useful for reference until you
become well acquainted with the various lengths, thicknesses,
numbers and prices. The card will contain one of each kind, with
price and number attached.

If you fix a butterfly with the ordinary pin, you may find the
latter partly covered over with verdigris after a time. This bright
green substance is formed by the action of decomposing animal
matter on the copper of the pin, and gives a very unsightly appearance
to the specimen. To avoid this the entomological pins are
either silvered, blackened or gilded. The silvered pins tarnish
after a time, but the two other kinds keep their colour well, and
are therefore better. The gilded ones are rather expensive and unnecessary,
and perhaps the black ones are to be preferred to the
silvered, although they are rather more costly.

Most dealers will supply you with a box of mixed pins, each box
containing about six different sizes. This is very convenient for
those who work in a rather small way; but if you intend to make
entomology a prolonged study you had better get an ounce or so of
each of the more useful sizes.

Butterflies vary much in size, and Nos. 3 to 8 are the most
useful sizes of pins to fix them; No. 3 being for the largest, and 8
for the smallest.

Supposing all the foregoing requisites to be quite ready, still you
are really by no means prepared for all your work. The butterflies
captured should be set as soon as possible after your return, and
everything required for this part of the work must be in perfect
trim. Yet I think it will be more convenient just now to confine
our attention to the subject of ‘Catching Butterflies,’ leaving all
the indoor work to form the substance of another chapter. Our
next point, then, shall be the consideration of seasons, times, and
localities.

The earliest of the butterflies make their appearance on the
wing in April, or, if the weather is mild, towards the end of March;[Pg 77]
and from this time you can find employment up to the end of
September or the beginning of October—a period of about seven
months. But it must not be supposed that all parts of this long
season are equally prolific, and will yield equally valuable catches.
Remember the short term of a butterfly’s life, and bear in mind
that each one has its own regular season in which to spend the
winged state; you will then see that anyone who wishes to ‘work’
as many species as possible must arrange his outings in accordance
with the insects’ own times.

Some butterflies are double-brooded, and the two broods may
not come forth at certain fixed times. Hence they seem to be on
the wing almost without cessation for several months together, and
therefore need not have a special day set apart for them. But
others are more uniform in their date of appearance, and die off at
about the same time. To catch such as these you must be careful
to watch the weather, make allowance for any severities that may
tend to cause a delay, or an unusually high temperature that may
hasten their emergence, and then select a day in which you may
expect to find them fresh and unworn. A week too early, and none
are to be seen; a week too late, and nearly all you catch are worn
and worthless.

A glance at our Calendar (Appendix II) will give you a few
illustrations in point. Thus you will observe that May is a month
for the ‘Whites,’ early ‘Blues’ and certain of the Fritillaries;
July for most of the Hairstreaks and Browns, and so on. Before
you have been long collecting you will have captured the very
common species, and then you will find that your butterfly hunts
are very unproductive unless you make it a point to try for certain
species at the proper times.

Time, however, is not the only thing to take into account when
preparing for a day with the butterflies. It is equally important
that we should carefully select our locality in accordance with the
known haunts of the various species. As long as you are simply
working up the common kinds, you may wander almost at random
in waste places, flowery meadows, corn fields, railway banks, &c.;
but when you have secured a few specimens of each of these, you
must search out the favoured resorts of the more local and the
rarer species. For instance, wooded spots must be visited if you
are to take certain of the Fritillaries, oak woods for the Purple
Emperor and the Purple Hairstreak, fenny districts for the beautiful
Swallow-tail, and so forth. In some cases the butterflies are[Pg 78]
closely restricted to certain isolated localities, to which you must
travel if determined to obtain them.

There yet remains another important matter to consider, and
that is the kind of day you shall select for your outing. Butterflies
are not only strictly day-fliers, but most of them venture out only
on bright days. Always choose as hot a day as possible, with a
very bright sun. If you are to be out for a full day’s collecting,
manage to be on the hunting ground at about ten o’clock in the
morning. As a rule there are not many out before this time, and
some do not appear to stir till an hour later: still there are a few
‘early birds’ among them, one of which—the Wall Butterfly—I
have seen on the wing before eight.

If your season, your day, and your locality are all well chosen,
you may reckon on a good six hours’ work. At about four the
butterflies begin to lag, and then drop into their hiding places, one
by one, till only a few of the late stragglers remain on the wing.

So far I have furnished some general instructions that may be
regarded as preparatory to the start; but I will now give a few
hints as to the mode of procedure when the day for field work has
come.

First, see that you have secured all your apparatus, and that it
is in perfect condition. What is more annoying than to find, after
you have travelled some miles to get to your hunting ground, that
you have left your screw ferrule at home, or that the soldering of
your metal Y is just giving way? If you are troubled with a short
memory, it will be advisable to make out a list of every requisite
for your field work, and keep this for reference on all field days.

Here is a list of your equipment for a day with the butterflies.
Net, ferrule or Y, stick, collecting box (the cork of which should be
damped if the box is a metal one), a few ‘chip boxes’ for live
insects, killing apparatus, a good supply of pins of several sizes, a
piece of string, needle and cotton, and your penknife.

You observe in this list one or two items not previously mentioned,
since they hardly come under the category of apparatus,
but a moment’s thought will convince you of their usefulness, especially
in the case of a breakdown. If your net catches in a thorn—a
very common occurrence—and a big rent is made, the needle and
cotton will save you a deal of agony, and perhaps loss of temper.
If your stick breaks under your exertions, the knife or the string
may prove a most valuable companion. Your pins may be stuck
in the cork of your collecting box, certainly the most convenient[Pg 79]
spot for immediate use; but you may also have a reserve store in
a small pocket cushion, or arranged neatly on a strip of flannel
which can be rolled up in the waistcoat pocket.

At last you are on the hunting ground, fully equipped but inexperienced,
and at first find yourself just a little awkward in the
use of your new gear. Your experience with the cap has been a
very wide one, and you are possibly an expert at knocking down
‘Whites’ in the streets and in your neighbour’s kitchen gardens.
Now you have to wield the net, and coax your captives into your
killing bottle; hence a slight feeling of incompetence at first.

You soon get over this, however, and within five minutes you
may be seen furiously slashing away at all the poor butterflies that
come within range, common ‘Whites’ and dingy ‘Browns’ receiving
as much attention at your hands as any rare gem that
may happen to cross your path.

How different are the movements of an experienced collector!
He walks stealthily along the route he has chosen, apparently
taking but little notice of the majority of butterflies that approach
and pass him. He has already secured his ‘series’ of nearly all
the species, and is carefully on the watch for the gems that are
required to complete his cabinet. His actions are slow and deliberate
rather than rash; and he trusts more to his eyes than his
legs.

The beginner may take to his field work quite to his own satisfaction,
and may travel homeward with a feeling of great pride over
his first day’s catch; but yet there are a few points in which a little
advice may not be quite out of place, particularly so with regard to
the management of the net, and the killing and pinning of the
insects.

Most of the butterflies may be caught on the wing, and it is far
better to net them in the air than to sweep them off the herbage
and flowers. If these are rather low, you should strike the net
smartly upwards from below them, but of course this movement is
impossible with insects that happen to be almost above your reach.
If a butterfly is busily engaged in searching out its sweet food,
flying from flower to flower, don’t think of giving chase, but follow
it up stealthily, and you will sooner or later get an opportunity of
striking at it while in the air. Sometimes, however, you will see a
powerful flier making a straight dash across your field, taking no
notice whatever of the fragrant blossoms, but evidently engaged on
some important errand. If such happens to be a species you[Pg 80]
require, then you must run for it, but you will probably be satisfied
with only a few chases of this kind, particularly if the sun is very
hot, and the ground diversified with clumps of furze, heather,
‘molehills,’ and ditches.

There are times when your only plan of netting a butterfly is
to sweep it from a flower or leaf on which it has settled. If the
vegetation is very low, you have simply to bring the net down upon
it, and then, holding up the apex of the net with the other hand so
as to give it room to fly, you can inclose it by grasping the lower
part of the net as soon as the butterfly has fluttered upward. If
the herbage is tall it is advisable to strike either upward or sideways
at the insect, starting it from the leaf or flower on which it rests;
for if you bring down the net you will have to inclose the whole or
part of the plant on which the butterfly has settled—a procedure
that often ends in a torn net, or in the insect becoming damaged
through being rubbed against the plant.

Whenever you capture a butterfly by a sweep of the net
through the air, you immediately turn the ring into a horizontal
position, so that the bag of the net closes itself as it falls over the
edge. This gives you an opportunity of examining the insect before
you introduce your killing bottle. This is a very necessary precaution,
for you are generally unable to judge of the condition of a
butterfly while on the wing, and in some cases you cannot even be
certain of the species. If, then, you were to call the killing bottle
into requisition for every capture you make, you would certainly
find yourself taking the life of many an insect that is of no use
whatever to you. Always examine your specimens at the moment
they have been secured, at least as far as it is possible to do so, by
looking through the gauze; and let your examination be as brief as
possible, or some of the butterflies that were at first in splendid
condition will render themselves useless to you during their
struggles to get away.

When satisfied that an insect is likely to be of value to you, keep
it in the apex of the net by grasping the bag beneath it with the
left hand, and then introduce the opened killing bottle with the
other hand. As a rule you will experience not the slightest difficulty
in coaxing it into its trap, and then you quickly cover the
mouth of the killing bottle with the gauze, then apply your left
hand, using it as a temporary stopper for a few seconds, and now,
the insect having been quieted, replace the cork.

A good killing bottle is almost instantaneous in its action, not[Pg 81]
only stupefying, but immediately killing the insects; and as soon as
you are sure that each specimen is quite dead, you may pin it in
your collecting box.

You must be cautious, however, on the one hand, that you do
not take it out too soon. If you do you may find that it recovers
from the mere stupefying effect of the poison, even after it has been
pinned, and when you open your collecting box for the next butterfly,
you are horrified at the sight of the poor victim struggling to
free itself.

On the other hand, don’t keep the insects in the killing bottle
too long. If you do you will soon have a number, one lying on
another, and all tumbled about together while you are on the chase.
Of course, under such circumstances you are sure to damage them
more or less.

Many collectors, although they may always use a killing bottle for
moths, never employ one for butterflies, but kill them by pinching
the thorax. It is well to know how to do this, for it sometimes
turns out to be a really quicker process than that we have just been
considering; and, more than this, you can resort to it should you
break or lose your bottle while in the field. It is done in this
manner: Bring the two opposite sides of the net together, closing
them on the insect so that it cannot flutter. If now the wings are
brought together over the back, all is right, but if not, give it just
a little room to flutter till you have the opportunity of closing the
gauze upon it with the wings in the desired position. Now pinch
the thorax smartly between the finger and the thumb, applying the
pressure outside the net, but be careful not to squeeze the abdomen.
In a moment you will find the insect quite dead, and not in the
least damaged unless you performed the operation clumsily.

Now as to pinning. Hold the dead butterfly between the finger
and thumb of the left hand, and pass a pin of convenient size through
the centre of the thorax above, and push it through so that the point
appears centrally on the under surface. It is now ready for your
collecting box.

So you work on till the sun begins to get low, and the butterflies
become fewer and fewer, till only a few stragglers of common species
are to be seen. Still there are a few hours of daylight and perhaps
even of bright sunshine before you, and if you are not weary with
the work done, you may very profitably spend these hours in the
collection and study of the habits of moths.[Pg 82]

Catching Moths by Day

The reason for choosing the sunny hours for butterfly collecting
is obvious, all these lovers of brightness being then actively on
the wing; and although many may be driven out of their hiding
places by beating the herbage with the handle of your net, or even
be searched out as they rest on stalks and leaves during dull days
or at morning and evening twilight, yet such methods are comparatively
tedious and unproductive.

Some moths also are lovers of sunshine, and while engaged in
butterfly hunting you will often meet with a moth flying briskly
from flower to flower and taking its fill of both sweetness and
brightness. Again, as you wade among flowery herbs in quest of
butterflies you will certainly disturb a number of moths, causing
them to take a short flight in search of a safer spot. Thus you will
almost invariably find a few moths among the contents of your
collecting box even though you made no special effort to seek
them out. But we shall now see how we may set to work to
obtain a successful catch of moths at times when butterflies are
not so much in demand, or during the less brilliant hours of the
day, when butterflies are at rest.

The apparatus required for this work need not differ in any important
respect from that recommended for butterflies. The same net is
used, any reliable killing bottle will do, and the pins and collecting
box used for butterflies are equally serviceable. But your mode
of procedure is very different.

As you walk towards your proposed hunting ground you will
do well to examine the trunks of trees, old walls, and wooden fences.
In this way you will meet with moths fast asleep, which are
consequently easily taken. All you have to do is to hold the open
killing bottle obliquely just below the insect, and then push it
gently downward with a small twig or stalk. As a rule the moth
will drop direct into the bottle and make no attempt to fly away;
but some are very light sleepers, ready to take flight at the slightest
disturbance; and when dealing with these you must be careful to
bring the mouth of the killing bottle so closely round them that
there is no room for flight except into the bottle itself. It is well,
however, not to take long at this kind of searching, but to reserve
as much as possible of your time for what you consider to be a
very favourable locality.

Speaking generally, a good locality for butterflies is a favourable[Pg 83]
one also for moths, and you will do well to give special attention
to well-grown hedges, especially those that surround clover fields;
also overgrown banks, the borders of woods, open spaces in woods,
the trunks of isolated trees, gravel pits, and old chalk quarries.

Walk beside or among the undergrowth of woods, or among the
tall herbage of waste places, tapping the branches and twigs with
the handle of your net as you go. Then, if your locality is well
selected, you will rouse moths to flight at almost every stroke.
Some of these will shoot upward among the lofty branches and
disappear quite beyond your reach; others will fly rather low and
somewhat heavily, giving you favourable opportunities to try your
skill with the net; others, again, will fly only a yard or so, and
alight on a neighbouring leaf, often remaining so quiet that the
killing bottle is easily made to inclose them.

There are moths that show a decided preference for large trees.
These may be seen hovering about high branches during the evening
twilight, and sometimes even in sunshine. In many such
cases the chance of a capture seems hopeless, but occasionally one
will descend so low that a watchful collector is able to secure it by a
sweep of the net.

If at any time you are in a locality by day where you suspect
the presence of certain species of moths at rest among the upper
branches of trees, such branches should be beaten if possible to dislodge
the insects they may shelter. A long stick will often serve
this purpose well, and, failing this, a few stones thrown among
the branches may prove effectual. In the case of small and rather
slender trees, a kick against the trunk will set the whole in vibration
sufficient to surprise all the lodgers; and the same effect may
be produced with larger trees by giving each a good sound blow
with a mallet or some other suitable implement.

This or any other plan of ‘beating’ for moths is much more
conveniently worked by two collectors together than by one alone;
for one engaged in beating the herbage cannot be at the same
time fully on the alert with the net. If two persons are together,
one may take the lead, armed with the beating stick only, while
the other, only very slightly in the rear, is always ready to
strike.

We have said that butterflies should always be killed in the
field, but this plan is not so universally adopted with moths. Many
collectors carry a large supply of pill boxes when going out for the
latter and then take as many as they possibly can by boxing them[Pg 84]
direct in these. This method of ‘pill-boxing’ is very simple in
the case of the lazy and soundly sleeping moths. It is only
necessary to hold the open box below the insect, and then cause
it to fall by pressing the lid down gently on it from above.

Many of the moths so caught will remain quiet in the boxes
and can be taken home alive without much fear of damage. All
may then be killed at the same time by packing all the pill
boxes in some vessel of sufficient accommodation, and shutting
them in with a little chloroform, ammonia, benzole, or other
suitable poison. The vapour will soon find its way through the
pores of the pill boxes, but, in order to make its action speedy,
each one should have a few perforations in the lid.

Whatever advantages this method may give to the collector
who works at night, when the process of pinning would be more
or less tedious, there is no necessity for its adoption during the
day. The large number of pill boxes required is certainly far
more bulky than the single collecting box that would accommodate
all the day’s captures; and although most of the insects boxed
alive may be none the worse for the shaking they get, and may not
damage themselves by fluttering in their small prisons, yet there is
often a little loss on this score.

If you do adopt the pill-boxing method, be very careful
that you do not mix the occupied boxes with the empties; and unless
you fix on some definite plan for the prevention of such an
occurrence, you will often find yourself releasing a prisoner from a
box you have just opened to receive a new-comer.

Suppose that you start with all your empties in your right
pocket. Then each one, as soon as it is tenanted, might be placed
in the left, with the name of the insect, or any particular concerning
it you would wish to note, pencilled on the lid.

When examining the trunks of trees you will be continually
meeting with specimens of very small Moths—Pyralides, Crambi,
Tortrices, and Tineæ—and at first may find some difficulty in
boxing or bottling such small and delicate creatures. A grass
stalk will enable you to tip some of them into your killing bottle,
but some are so snugly packed in crevices of the bark that it is
almost impossible to get them out without damage, even with a
thin and slender stalk. But a sudden puff of wind from your
mouth will often be sufficient to dislodge them and blow them
into your net, and from this they are easily transferred to a box or
bottle.[Pg 85]

These few hints will prove sufficient to start you on moth-hunting
expeditions during the daytime, and will enable you to
make good use of the dull days and cloudy hours when the butterflies
are quiet; but we must now turn our attention to the night
work of the entomologist, and see how we may attract and catch
moths during their hours of work and play.

Searching for Moths at Night.

It is a well-known fact that the night-flying moths are attracted
by lights, a characteristic of these insects that it is difficult to
explain. Their love of darkness is in many instances so decided
that they absolutely refuse to take flight while the fading light of
day still lingers on the horizon, and even display a great aversion
to the rays of the moon; and yet these very same species will
often rush madly into the fierce glare of a naked artificial light, or
fly with an energy almost amounting to fury against the glass of a
street lamp or lighted window.

Puzzling as this peculiar tendency is, we can profitably turn
it to our own account by making it a means of luring a number of
moths into our presence.

The simplest way of putting this mode of capture into effect is
to post yourself at your open window, with net and cyanide bottle
at hand, while the brightest light you can command casts its rays
as far and as wide as possible into darkness outside. If you use
an oil lamp for the purpose, let it stand just inside the window
frame, or, if a jointed gas bracket happens to be situated beside the
window, bend it round so that the rays may pass over a wide area
outside.

Two such lights are sometimes a very decided advantage—one
quite outside the window to attract the moths from all possible
points, and then another near the middle of the room to invite
them inside. Whether you use either one or two lights, always
see that it or they are so surrounded by a screen that the moths
cannot by any possibility rush into the flame. There is nothing
better for this purpose than a covering of light gauze, for this is
not only a barrier for the prevention of the suicidal tendencies of
the insects, but it also gives a good foothold to those who would
like to rest and enjoy the luminous feast.

You will soon begin to learn that moths, like ourselves, exhibit
great differences in their ways of enjoying their festal moments.[Pg 86]
Some will satisfy themselves by flying near the light in almost a
straight course, hardly slackening their speed as they pass; or will,
perhaps, make a hurried curve round the light and then pass on at
once about other business. To catch these you must be always on
the alert, with net in hand, ready to make a dash at the right
moment. But many will make straight for the flame, and then,
finding a barrier in the form of gauze or glass, will either flutter
round and round as if dissatisfied with your attempt to save them
from an untimely end, or else settle quietly on the screen to enjoy
the brightness for a long period. The flutterers are usually easily
covered by a glass or the open cyanide bottle, and as for those that
settle down quietly, you can take them at your leisure.

It will not do for a collector to depend solely on this method of
obtaining moths, but at times when either his duties or the bad
weather keeps him at home it affords him a means of capturing a
few specimens that otherwise would have been missed. He may
be even so busily engaged in other matters that he cannot afford
the time to stand and watch with net in hand, but the insects that
fly into his room and dance round the gas jet or inquisitively
examine the white surface of the ceiling are easily netted or boxed
without much loss of time.

The chances of success at this kind of work will vary considerably
with the aspect, the season, and the weather. If your
window opens on a large flower or fruit garden, on a patch of
wooded country with plenty of underwood, a piece of waste ground
overgrown with rank vegetation, or a stretch of heath or moor,
then you may expect a very large number of visitors; but if you
are situated on a level and barren country, or in the dense
atmosphere of a thickly populated district, you must not reckon on
many intruders.

As regards the season, this is more extended than that of the
butterflies. A few species of moths may give you a call during
the bleak nights of October and November, and also during the
somewhat less dismal nights of February and March; but from
April to September you may rely on a goodly number of captures.
Of course you will not expect many of the ‘rarities’ and ‘gems’
to find you out; these are to be searched for in the open field in
the manner to be presently described; but your lights will attract a
large number of the commoner species of Geometræ and Noctuæ,
the former chiefly during the early summer, and the latter more
or less throughout the season.[Pg 87]

A little experience will show you that the atmospheric conditions
form a very important consideration. The dark and warm
nights are the most productive. Very little luck is to be anticipated
when the full moon is throwing down her silvery rays from a clear
sky; nor will you see many while a cold east or north-east wind is
blowing. Under these conditions many moths prefer to keep in the
sheltered nooks where they slept away the sunny hours of the day.
They love a warm and moist air such as calls forth the odours of
the fragrant blossoms that provide their sweets, and show no dislike
to a fine drizzling rain that you yourself would prefer to avoid. A
pelting shower will generally keep them under cover, but they
delight in the fresh and moist air that immediately
succeeds the passing storm.



Fig. 50.—Frame
of Net for Collecting
Insects
on Lamps and
Windows.

If you reside on the outskirts of a town an
occasional tour of inspection of street lamps
may add a few specimens to your collection, and
some entomologists attach so much importance
to the value of these luminaries that they provide
themselves with a special net for the removal of
moths from the glass and rails (fig. 50). The
straight side marked a is applied to the panes
of glass when flutterers or settlers are to be
taken, and the bend on the opposite side is to
secure those that rest on the rail. Such a frame
is easily made by bending a piece of stout wire
to the required shape, and then soldering it to a
ferrule to receive a long stick. The net itself
should not be deep.

Many different forms of traps are now made for catching
moths, and these are deservedly coming rapidly into favour. They
are generally constructed on a ‘catch-’em-alive-oh’ principle, and
have the advantage that, after having been set, they may be left alone
all night without any watching, and give an ambitious collector the
opportunity of taking insects in his garden and searching in the
open field both at the same time.

One of these traps may be constructed as follows at the cost
of only a few pence over the price of a small paraffin lamp. Put
together a square box, the sides about two feet and the front open,
or procure a suitable one from your grocer. Place a paraffin lamp
with a bright tin reflector at the back of this, and make a hole in
the top just over the chimney to allow the heated air to pass out[Pg 88]
freely. Three sheets of glass are now to be placed as shown in the
sketch (fig. 51), one upright piece completely shutting off the lamp,
and two others placed obliquely with a space between them just
large enough to allow admission. These must be exactly the
width of the box, and should not be permanently fixed, but simply
resting on small wooden supports nailed on to the sides. When required
for use, it is only necessary to light up the lamp, strew some
dead leaves on the bottom of the box, and put the sheets in their
places. It will be seen at once that the angles at which they are
placed will direct all light-seekers into the lower compartment,
whence they are not at all likely to find their way out again; and
after vain endeavours to reach the light they finally settle down on
the sides of the box or seek shelter among the dead leaves.



Fig. 51.—A Trap for Catching Moths.

Occasionally it happens
that an entomologist
is lucky enough to claim
the friendship of a person
who, from the nature of
his calling, is peculiarly
well qualified to render
him great assistance.
Thus a friendly lamplighter,
expert and patient
in the use of the cyanide
bottle or pill box, is capable
of giving valuable aid at
times; and the keeper of a
lighthouse has it in his power to capture many a gem that is seldom
seen on the wing; but, although much may be done by means of
these and other stationary lights, this kind of work does not compare
favourably with the night rambles of a naturalist in the very
haunts of the objects of his search.

For such out-door work in search of moths a good lantern is
essential. An ordinary ‘bull’s-eye’ is almost useless, for, although
it concentrates a good light on certain objects, the narrow range of
its rays constitutes a strong objection to its use for entomological
work. For this purpose it is necessary that the rays of light not
only pass in front of you, but also shoot off right and left to warn you
of the approach of a moth before it is too late to wield the net.
This wide range may be obtained by means of three flat glass sides,
or, better still, by a bent plate glass front.[Pg 89]

In addition to this you must go out provided with your net,
killing bottle, and a number of pill boxes. Choose your night
according to the hints already given, and if you are on the look-out
for any particular species, be careful that the date of your outing is
well timed, making any necessary allowances for the forwardness
or backwardness of the season, for a moth that is generally due on
a certain average time of the year may appear some weeks sooner
if the preceding weeks have been unusually warm, or its emergence
may be delayed considerably by the prevalence of cold east
winds or a late frost.

Make up your mind as to the field of your operations before you
start, and if possible choose a route that will carry you through a
variety of situations, so that you may pass the favourite haunts of
a number of different species. Clearings in woods with an abundant
undergrowth, waste places with plenty of tall and rank vegetation,
overgrown railway banks, clover fields, the flowery borders of corn
fields, plantations in parks, heaths and moors, sheltered and overgrown
hollows such as chalk pits and old disused quarries, reed and
marsh land, all these are good localities, each one inhabited by its
own peculiar species, and if your route runs through a fair variety
of such places you may, other things being equally favourable,
depend on a good catch.

See that your time also is well chosen. Of course you cannot
say exactly what the night will be till it actually comes, and, as
you have to start off before it is dark, you must consider the
probabilities of the future from the present condition of the air. Let
it be a night when a bright moon is not due, and if it follow a
warm and moist day with a south or south-west wind, or if drizzly,
so much the better; but let your feet be shod with boots that will
permit you to wade through moist herbage without danger, and
take a waterproof if necessary.

It is always advisable to be on your hunting ground before
twilight sets in, as a number of moths venture out before the sun
has disappeared; and then you can work on till midnight if you
feel inclined, or even extend your labours till the early hours of the
morning.

Before dusk you will meet with many of the little Tortrices
(page 298) in sheltered spots, and a little later the Geometræ and
Hawks will be on the wing. Thus, before dark, you may make
good use of your net, dealing with your captures just in the same
way as recommended in the case of butterflies.[Pg 90]

After a time, however, the lantern will have to be brought to
your assistance in making known the whereabouts of the later
species, consisting chiefly of the Noctuæ, many of which do not
make their appearance till it is quite dark. If now you carry your
lantern in your left hand, your work will be rendered somewhat
difficult and tedious, for, although one hand is sufficient to manage
the net properly, you are compelled to rest your light on the ground
every time you make a capture, as it is impossible to box your
specimens unless both hands are quite free. This difficulty is easily
overcome by suspending the lantern by means of a string or strap
placed round your neck, allowing it to hang on your chest; and a
further advantage is gained by having a second strap round your
chest to prevent it from swaying about with every movement of
your body. This arrangement gives you both hands perfectly free
during the whole time, and also prevents the necessity of continually
bringing yourself into a stooping or kneeling posture
while you are examining or boxing the specimens you have
netted.

There are now two courses open to you. Either you can kill
and pin the moths as you catch them, fixing each one securely in
the collecting box, or you may simply shut each one in a separate
pill box and leave the remainder of the work to be done at home.
If the ordinary collecting box only is used, a little of your time is
necessarily occupied in pinning and transferring, and if many
insects are about such an occupation may appear to you to be a
waste of valuable time. But this is not all. Often and often will
you find that while thus engaged a splendid moth will come and
flutter round your light; and, before you have time to drop your
collecting box and pick up the net, the fine creature you would
have prized has darted off again. This certainly seems to speak in
favour of the pill-boxing method, but it must be remembered that
a few of the moths will continue to flutter after they have been
boxed, so that when you arrive home they are more or less
damaged, a large number of the scales that once adorned the wings
now lying on the sides and bottom of the boxes. Perhaps the best
plan is to take both the collecting box and also a quantity of pill
boxes, and a little experience will soon show you which is the
better accommodation for certain kinds.

Particular attention must be paid to flowers, some of which are
very attractive to the Noctuæ especially. Sallow blossom in spring
and ivy bloom in autumn should be carefully and frequently[Pg 91]
watched, and at other times the blossoms of heather, ragwort,
bramble, clover, and various other flowers must be searched.

As you cast the rays of the lantern on the feasting moths some
will prove themselves very wary, and dart away at your approach;
but others will take but little notice of your advance, and will
continue to suck the sweet nectar, their eyes glaring like living
sparks.

As a rule the Noctuæ thus engaged are easily pill-boxed or
caught direct in the cyanide bottle; but a few of the more restless
species are to be made sure of only by a sweep of the net. Some
will feign death as soon as disturbed, and allow themselves to drop
among the foliage, where further search is generally fruitless.

Another common difficulty arises
from the inconvenient height of many
of the attractive blossoms—often so
great that it is impossible to reach
them with the net, and very difficult
to direct the rays of your lantern on
them. This is particularly the case
with sallow and ivy, the
flowers of which are two
rich sources of supply
to the entomologist.



Fig. 52.

Fig. 53.—Net and Lantern
for Taking Moths from
High Blossoms.

Those who intend
giving special attention
to these blossoms should
be provided with some
form of apparatus that
will enable them to extend their operations as high as possible.
Perhaps the most effective arrangement is the well-known combination
here figured. It consists of a long and stout stick, at the top of
which is a tubular joint (fig. 52) that might be termed a T-piece
were it not that the smaller part does not stand out at right angles
to the other. In this is fixed, in a straight line with the stick, a
short rod on which hangs a lantern—an ordinary bull’s-eye answers
well here; and in the smaller tube is another short rod carrying a
shallow basin-shaped net, and of such a length that the net is just
in advance of the lantern.

At first sight this arrangement will strike you as being very
unsatisfactory, there being no kind of trap to prevent the escape of
the insects. But it must be remembered that moths are more or[Pg 92]
less addicted to habits of intemperance—that they will hold on to
the supply of the sweet fluid they enjoy till they are ready to drop
with intoxication. This being the case, some will fall into your
net as soon as they are startled by the sudden and near approach
of the glare of your lamp, and others are easily made to fall therein
by gently tapping the flower-bearing stems from below with the
edge of the ring.

Having become acquainted with this very sad propensity, which
thus brings ruin to so many unfortunate moths, can we not yet
further turn their evil doings to our own profit in our endeavours
to become acquainted with their structure and history? Most
certainly we can. All we have to do is to distribute in their haunts
a bountiful supply of some artificial intoxicant such as they love,
and then lie in wait for the victims that fall a prey to our snare.
This process is known to entomologists as ‘sugaring,’ and is a
splendid means of securing an abundance of species, often including
some rare ones that are scarcely to be obtained by any other plan.
Let us now inquire into the modus operandi of this interesting
operation.

The first thing to do is to prepare the luring sweetmeat. Supply
yourself with a quantity of strong, dark treacle, and also some dark
brown sugar; always remembering, in the selection of these viands,
that odour rather than purity is to be the guide. The best kinds of
sugar are those very dark and moist brands imported in a raw state
from the West Indies, nothing being better than that known as
‘Jamaica Foots.’

Mix about equal quantities of these with a little stale beer, and
boil and stir till all the sugar is dissolved. The consistency of the
mixture should be such that it will work well with a brush when
used as a paint—not too thick, nor so thin that it is easily
absorbed by the substance on which it is ‘painted,’ nor must it be
in such a fluid condition that it easily runs.

When satisfied on these points, transfer the mixture to a tin
canister, see it properly covered, and set it aside as your ‘stock’
from which you can draw supplies as required. Now secure an
ordinary painter’s brush of convenient size, and a number of strips
of linen or other rag, each one of which is fastened to a hook formed
of bent wire. These items, together with the usual lantern, collecting
box, pill boxes, and killing bottle, complete your outfit for the
sugaring expedition.

When the selected time for operations has arrived, take sufficient[Pg 93]
‘sugar’ for your night’s work, mix it well with sufficient
strong rum to give it a very decided odour, and start off at dusk
with this and the other requisites just mentioned.

The night chosen should be warm and calm, with a rather damp
atmosphere, and no moon preferred. Let your locality be a well-wooded
one; abounding, if possible, with giant oaks and other trees,
and containing open spaces with plenty of underwood and rank
herbage. Such localities are to be met with at their best in forest
lands, and if you would do wonders at sugaring you cannot do better
than arrange for spending your holidays in such a spot as the New
Forest, taking with you sufficient ‘sugar’ for several nights’ work.

Having reached a likely spot of no very great extent, you prepare
for real work. Light up the lamp, and get out your sugaring
tin and brush ready for action. Take your course along some
definite track that you are sure to remember, painting vertical strips
of sugar, about a foot long, on the trunks of trees or on palings,
and hanging strips of rag that have just been steeped in the sugar
on the branches of small trees and shrubs where you do not find
good surfaces for the brush.

After satisfying yourself concerning the amount of sugar distributed,
retrace your steps, examining every patch of sugar as you
go. It will not be long before signs of life appear. Earwigs, spiders,
centipedes and slugs will soon search out the luscious feast, but
unless the time and the locality are ill chosen, the lantern will soon
reveal a goodly number of moths, with eyes glaring like little balls
of fire, greedily devouring the bounteous repast. These will consist
chiefly of Noctuæ, but Sphinges, Geometræ and numerous small
species also join the company.

Some will exhibit a restless disposition, either darting off before
you make a close approach, or keeping their wings in rapid vibration
as if to be fully prepared for a hasty retreat when occasion demands.
These must receive your attention first; and, having secured them,
proceed to box as many as you require of the more lazy and
gluttonous species.

As a rule, moths thus engaged are easily pill-boxed, but the
livelier ones will not submit to such treatment without attempting
to escape. The best way to secure these is either to cover them
with the opened cyanide bottle (or its substitute), and replace the
cork as soon as a favourable opportunity occurs; or to perform the
same feat with a glass-bottomed pill box.

The advantage of the latter over the ordinary boxes will be[Pg 94]
seen at once. After the insect is covered, its movements can be
watched, and so a favourable opportunity can be seized for snapping
on the lid.

As already stated, some moths feign death when in danger,
allowing themselves to fall in places where they are often quite safe
from capture. Others allow themselves to fall simply because they
have so gorged themselves with the intoxicating sweet that they
can no longer maintain their hold. Both these classes of sugar
seekers may easily be secured by means of a net commonly known
as the ‘sugaring net.’



Fig. 54.—Frame
for the Sugaring
Net.

This implement is so simple in its construction that anyone can
easily make his own. The frame may consist of two straight
wires or canes fixed in a metal Y, and the other ends joined by a
piece of strong string or catgut as shown in fig. 54. The net itself need
not be deep. As soon as you reach a tree where moths are feeding
on the sugar, press the string of the net against
the bark just below them. The string at once
assumes the form of the trunk so well that you
may be sure of every insect that falls while you
are boxing.

For this work both hands must be free, and
this is easily managed in spite of the number of
appliances called into service. The lantern is
slung round your neck and secured by a strap
round the chest. The ‘sugaring net’ has a very
short stick, and just while you are engaged in
boxing specimens, it may be gently held against the trunk by a
slight pressure of the body. But such precautions as these are
necessary only when the night worker is out alone. There are
many circumstances, however, that render the work of two or more
in company much more enjoyable than that of a single-handed
entomologist. The labours are considerably expedited where a
division enables each one of the night ramblers to take a particular
portion of the work; and if there is such a person as a nervous
entomologist, that individual should on no account go a sugaring in
lonely spots on dark nights. Every rustling leaf gives such a one
a start; all footsteps are those of approaching disturbers of the
peace; and when at last the invisible landowner or his keeper,
attracted by the mysterious movements of the lamp, greets him
with his gruff ‘What’s your business here?’ then for the moment
he forgets his enchanting hobby and wishes he were safely at home.[Pg 95]

It is certainly advisable to take a friend, whether an entomologist
or not, on such expeditions; and if you intend working on private
grounds, always make previous arrangements with the property
owner, that you may fear no foes and dread no surprises; for a
sugarer is far more sure of success in his work if he keeps a cool
head and has nothing to think about for the time being but his
moths and his boxes.

A few hours at this interesting employment pass away very
rapidly, and when midnight arrives there is often no great desire to
leave off, especially when it is known that some species of moths
are not very busy till very late at night. Still it is not advisable
to surfeit oneself with even the sweets of life. Perhaps it is better
as a rule to work the early species only on one night, and reserve
another for the later ones. The searchings are then always carried
on with vigour throughout, and the labours that are thus never
made laborious ever retain their attractiveness in the future.

It has often been observed that, when sugaring has been carried
on for a few successive nights in the same locality, the success is
greater each night than on the one preceding it. Hence it is a
common practice to work a chosen ‘run’ for two, three, or more
nights in succession; and some collectors even go so far as to lay on
the bait for a night or two previous to starting work. For the same
reason it is often advisable to continue the use of a fairly productive
beat rather than to wander in search of a new one.

In the neighbourhood of large towns one may often meet with
patches of sugared bark that mark the course and extent of a
brother entomologist’s beat, and such are valuable to an inexperienced
amateur in that they give him some idea of the nature of
the localities that are chosen by more expert collectors. But it
must be remembered that each entomologist has a moral right to a
run he has baited, and that it is considered ungentlemanly, if not
unjust, to take insects from sugar laid by another. I have sometimes
seen cards, bearing the names of the collectors and the date of
working, tacked on to baited trees and fences, thus establishing
their temporary exclusive rights to the use of their runs. Such
precautions are not necessary in large tracts of forest land, where
the choice of runs is practically unlimited.

There are two other modes of capture available to the moth
collector—the use of decoy females, and the employment of ‘sugar
traps’—and both these may be used on the sugaring run, or at other
times either in the woods or in your own garden.[Pg 96]


Fig. 55.—Cage for
Decoy Females.

Fig. 56.—A Sugar
Trap.

The wonderful acuteness of the sense by which the males of
certain species are enabled to seek out the females has already been
alluded to, and the possession of a suitable decoy will often bring
you a number of beautiful admirers without the least trouble, except
that taken in securing the decoy and preparing her temporary abode.
It is absolutely necessary that the female moth be one that has
recently emerged, and consequently you had better secure her in
one of her earlier stages, either by previous rearing or by collecting
the pupæ.

A little cage composed of a framework of wire covered with gauze
must now be made. Perhaps the simplest pattern is that illustrated.
Here the gauze is attached to two wire rings, only a few inches in
diameter, and suspended by a string. Such a cage answers every
purpose in the field, and has the advantage of folding into an
exceedingly small space when not in use. It may be suspended in
your garden or taken into the field whenever you have a suitable
decoy at your disposal.

The sugar trap may be of much the same pattern as that in
which a light is used, but if intended for field work it should be of a
convenient size for portability. A lighter and far more convenient
form may be constructed as follows:

Procure a large cylindrical tin box, and cut a circular piece of
perforated zinc just small enough to drop into it. Then make two
wire rings, one a little larger than the top of the tin, and the other
only about an inch in diameter. Next make a conical net of leno,
open at both ends, and of such a size that the two rings may form
the frames of its two extremities. When the trap is required for[Pg 97]
use, cut a circular piece of flannel or other absorbent, steep it in
sugar that has just been flavoured with rum, and place it in the
bottom of the tin. Then place a few pebbles of equal size around
the sides to support the zinc partition, drop in the partition, and
then allow the net to hang on the rim as shown in the sketch.

This arrangement will explain itself. The moths, attracted by
the sweet perfume, flutter about in the net till at last they find their
way through the small ring. Once in, they make further attempts
to reach the sugar; and, at last, finding all efforts fruitless,
and, like Paddy at the fair, not being able to discover the ‘entrance
out,’ they finally settle down in a disappointed mood awaiting your
pleasure.

Perhaps another word of explanation is necessary here. Why
not allow the poor creatures to reach the sugar that attracted them
to the spot? The reason is this. They sometimes gorge themselves
to such an extent that their bodies, dilated to the fullest capacity
with syrup, are a bit troublesome when the insects are placed in the
cabinet. It is therefore advisable to see that the zinc is so far above
the sugar that the moths are unable to reach the latter by thrusting
their extended proboscides through the perforations. A few dead
leaves scattered on the zinc is also a useful addition, since it affords
shelter to such of the insects as prefer it.

This is a very useful trap to keep in one’s garden throughout the
season. It may not attract large numbers, but it has the advantage
that it requires no watching. It is simply necessary to set it at
dusk, and remove the captives in the morning or at your leisure.


[Pg 98]

CHAPTER VII

COLLECTING OVA, LARVÆ, AND PUPÆ

We have already observed that insects should, as a rule, be set as
soon as possible after their capture; and it would therefore seem
that this is the proper place for instructions in this part of the work.
But it so happens that butterflies and moths are to be obtained by
means other than those already described, and we shall therefore
consider these previous to the study of the various processes
connected with the setting and preserving of our specimens.

Were we to confine our attention to the capture of the perfect
forms only, our knowledge of the Lepidoptera would be scanty
indeed, for we should then be ignorant of the earlier stages of the
creatures’ lives, and have no opportunity of witnessing the wonderful
transformations through which they have to pass.

Such an imperfect acquaintance with butterflies and moths will,
I hope, not satisfy the readers of these pages; so it is intended, in
the next two chapters, to give a little assistance to those who would
like to know how to set to work at the collection of their eggs and
larvæ, how to search for the pupæ, and how to rear the insects
from the stage at which they are acquired till they finally emerge
in the perfect form.

These portions of an entomologist’s work certainly take up a
great deal of his time, and also require much patience and perseverance;
but the advantages derived cannot be over-estimated, for
in addition to the knowledge gained of the early stages of insect
life, this kind of work will enable him to place in his cabinet a
number of gems he would otherwise have not and probably know
not. Occasionally a prize may be obtained in the form of a cluster
of eggs (ova) of a rare species, in many instances the larvæ are to
be obtained with comparative ease, while the perfect insects of the
same species are not often seen or not easily captured, and many a[Pg 99]
rare pupa has been dug out of its hiding place during a season
when the entomologist had but little other work to occupy his time.

These and other similar subjects we shall now consider in turn.

Collecting Ova

The collection of ova may be carried on more or less throughout
the year. A number of moths are out in February, and even
in January if the weather is mild. These soon lay their eggs,
which are hatched about the time that the buds of the food plant
are breaking. From this time till late in the summer the ova of
various species are being deposited, the average period from laying
to hatching being from two to three weeks. Then, during the
autumn, when the leaves of food plants are turning brown and
crisp, ova are still being laid, but these remain unchanged till the
new buds of the following spring are bursting.

Of course if you intend searching for the ova of particular species
you must previously ascertain the favourite haunts of those species,
become acquainted with their food plants, and also with the season
or seasons during which the eggs are laid. But the few following
hints will suffice as general instructions for the search.

In nearly all cases we must expect to find ova on the food plants
of the respective species, but at times, especially with certain
moths, we may come across them in the most unlikely spots.
Thus, it sometimes happens that a moth settles on a street lamp,
and lays her eggs on the framework round the glass, or even on
the glass itself. The same thing may take place on the sash or
glass of a brightly lighted window.

Such occurrences, however, we must regard as accidental and
comparatively rare, and therefore we confine our searchings for ova
to the food plants of the species we require.

As a rule the under sides of the leaves will yield the most, but
we have already noticed (page 18) that some moths leave their eggs
exposed on the upper surface. Again, some larvæ feed on flowers
and seeds and fruit, and the eggs of such are deposited on these
parts. Those insects which feed on the leaves of shrubs and trees
often lay their eggs on trunks, branches and twigs. Sometimes
these are laid singly, sometimes in dense clusters; and it is not
unusual to find them arranged in rings or spirals with great regularity.
When examining the trunks of trees for ova it is necessary
to look well into the crevices of the bark, for some insects take[Pg 100]
particular care to lay them in deep sheltered chinks; but others
take no such precautions, and deposit them on exposed ridges or
plain surfaces where they are easily discovered.

One difficulty of the ova collector lies in the fact that many
insects lay on the upper branches of large trees. Of course a search
for these is out of the question; but in places where the trees have
been cut down a few years previously, and where a consequent
undergrowth has developed, there are considerable chances of
success with these species. Young saplings of trees often yield
well, especially in places where tall trees of the same species are
absent. It may be mentioned, too, that some moths (page 294)
actually lay their eggs beneath the surface of water, depositing
them on the under surfaces of floating pond weeds; and others
(page 298) even enter the nests of wasps and bees for the same purpose.
It is clear, then, from these few remarks, that the work of
an ambitious collector of insects’ eggs is by no means a monotonous
task; for his employment takes him into the meadows and
woods, leads him to the banks of ponds, and even compels him to
tear down banks and hedges for the nests of Hymenoptera at the
risk of a sting or two.

One of the most productive sources of eggs is undoubtedly the
possession of captured females. When you are out netting butterflies
you often see a female that is evidently engaged in her
matronly duties. Instead of seeking food from the various flowers
in her path, she pays attention only to the foliage, looking out a
suitable leaf on which to deposit her eggs. Should you meet with
an insect thus engaged which you would like to rear at home, or of
which you would like to know the egg, secure it in a perforated
pill box with a leaf of the proper plant; and it will often supply
you with abundance of eggs for your purpose, in many cases depositing
them in the box before you arrive home. The eggs of
numerous species of moths are also to be easily obtained from
captured females.

Some insects do not seem inclined to deposit their eggs in captivity
as freely as when at large, and in order to induce them to do
so we must, as far as possible, put them in their natural conditions.
Let them have plenty of room, and supply them with fresh twigs
of their food plants, kept green by standing them in vessels of
water. It is also advisable, supposing you are not well acquainted
with the dispositions of the species you have, to keep a portion of the
box well shaded from direct sunlight, and allow another part to be[Pg 101]
as bright as possible; for some species will not lay in a bright light,
while others will not do so without it.

Again, while some deposit their eggs within a few hours of
quitting the pupa case, others do not lay for several days. With
regard to the latter, it is frequently necessary to feed them while
in captivity, by placing in the box a piece of rag or sponge that has
been dipped in honey or syrup.

Each batch of ova should be carefully examined with a view to
knowing them by sight on a future occasion. A sketch should be
made in your note book, showing every detail that you can make
out with the aid of a good lens. Then observations concerning the
season, colour of the eggs, the situation in which deposited, arrangement,
and any other useful particulars, should be entered.

In the next chapter some hints will be given concerning the
management of ova and the rearing of the larvæ from the time of
hatching.

Collecting Larvæ

This occupation is generally far more productive to the
entomologist than searching for ova. The latter are very small,
usually well concealed, and to be detected only by a careful
scrutinising use of the eyes; but the superior size of the larvæ,
the frequent bright colouring, and the fact that they are easily
beaten from their hold, render the searchings of their hunters
comparatively easy and fruitful.

Before setting out on a larva-hunting expedition, there are a few
requisites to prepare. These include not only the implements for
your work in the field, but also the cages in which you intend to
rear your little captives. The latter are described a little later on
under the head ‘Rearing Lepidoptera,’ and the former we will now
briefly summarise.

The outfit must consist of a quantity of suitable boxes, a stout
hooked stick, a strong net, and a white material to place under the
herbage while you are ‘beating.’

‘Larva boxes’ are usually made of zinc, and have little sliding
doors in the lids, so that the lids need not be removed while out of
doors after the fragment of the required food plant has been
inserted. Such boxes are not by any means essential. Small tin
boxes will answer all purposes nearly as well, providing a number
of small holes be made in them for the admission of air. Chip
boxes are also fairly satisfactory, but these also should be perforated.[Pg 102]
The best way to do this is to push a red-hot iron wire
through the chip, making about half a dozen small holes in each
box. This method will give you clean holes of a uniform size
without otherwise injuring the boxes.

Metal boxes possess the advantage that they keep the food
plants moist for a long time, while chip boxes allow them to dry
rather rapidly. Yet there are some larvæ that do far better in the
latter, since such a quantity of moisture exudes through their skins
that they soon become uncomfortably wet if their apartment is not
well ventilated. Under these circumstances perhaps it is better to
take a supply of both, so that changes may be made as found
necessary.

One grave objection to chip boxes, however, is the weakness of
the material. They are easily crushed by pressure, and a bottom
or a top disc of wood often falls out; but this is easily overcome by
gluing narrow strips of calico round the top and bottom edges.
Chip boxes should always be treated in this way, and they will
then last five or six times as long.

Your supply of boxes should always include one large one of
metal in which to bring home a supply of food for the larvæ. If
you have a botanist’s vasculum, by all means take it, for nothing
can serve this purpose better. If not, any rather large square tin
box will do, and this may be carried in your satchel, or a couple of
hooks may be soldered to it so that a leather strap can be fixed for
slinging it over your shoulder.

The net required is that commonly known as the ‘sweep net.’
It must be very strong, for it has to submit to rather rough usage.
The frame must be made of thick wire; and the bag, which need
not be more than a foot deep, should be of strong calico or holland.

Now with regard to the white material previously mentioned.
This may be a square of calico, hemmed round the edges. Nothing
is more convenient than this, as it occupies but little room in the
pocket when not in use, if neatly folded. The material need not
be thick, but the larger it is the better. Many prefer a white
umbrella or an ordinary umbrella with a white lining, but as this
is only a matter of taste and convenience you must decide for yourself
as to which you will use.

If your field of operations is only a little way from your head
quarters, and quantity of luggage therefore not a serious consideration,
you may provide yourself with a heavy mallet, loaded if
necessary with a pound or two of lead. This will prove very useful[Pg 103]
in shaking larvæ from trees and large branches. Lastly, take a
pencil and a note book or writing paper for your observations in
the field.

Now for the choice of the season. Larvæ are to be found all
the year round. Early in the spring, as soon as the buds are
bursting, some break out of the eggs recently laid by the moths
that appear in February and March. Later on, during April and
May, a host of both butterflies and moths are busy arranging for
their broods. Then, throughout the whole of the summer, thousands
of caterpillars of all sorts and sizes are to be met with everywhere.
And finally, during the bleak winter months, you may
amuse yourself by digging the hybernators out of their hiding
places where they rest themselves till the spring sun again calls them
out to refresh them with the young and tender leaves of a new
year. Thus, unless you are merely intending to search out certain
species you happen to require, there is not much difficulty in
settling on the season.

The day selected should be dry, for your work lies among the
herbage of banks, meadows, and woods, and nothing is more unpleasant
than wading through a wet and dense vegetation, or beating
down on yourself a shower of large drops from the branches of
trees and shrubs.

Having reached the hunting ground, the first thing to do is to
look out for signs of the presence of larvæ rather than for the
larvæ themselves. Healthy vegetation with sound leaves must be
passed by as untenanted; but the presence of partly eaten foliage
immediately arouses suspicion.

A little experience will soon enable you to distinguish between
the ravages of larvæ and of slugs, snails, wasps, &c. Some of
the smaller larvæ certainly eat out clean holes like those cut by
Hymenopterous insects, but as a rule they bite away at the edges,
leaving the midrib and the larger veins standing out almost naked.

By looking well into the edges of the eaten leaves, it is easy to
see whether the marauders have been recently at work. If they
are dried up and discoloured, it is not of much use to search; but if
still green and moist, you may feel almost sure that the hungry
larvæ are not far off.

In this case you will carefully turn over the leaves to examine
the under sides, and also the leaf stalks and branches or stems;
but you must be prepared for all kinds of protective mimicry.
Little green caterpillars will be seen lying on the midrib or[Pg 104]
veins, so straight and so still that they are scarcely perceptible.
Others are snugly tucked in a depression of a leaf with the same
result. Then we must also be prepared for the artful little tricks
of the larvæ of Geometræ (p. 268), by which they imitate stalks
and twigs so closely that a sharp eye is necessary to discriminate
between the two.

While thus searching we may meet with the cast skin of a caterpillar.
This gives us fresh hopes, and so we continue our careful
examination. At last, on grasping a leaf in order to turn it over for
inspection, we feel something hairy or something soft and smooth.
But lo! it is gone. It is one of those numerous caterpillars that
feign death and drop to the ground on the slightest sign of danger.
We search below for it, but the density of the vegetation renders
this hopeless, and we are just about to start off in search of a more
productive locality when we espy a quantity of the excrement of
larvæ lying on a little bare patch of ground close by. This gives
us a new idea. Here is another indication of the presence of the
creatures we require, one that we can put into practice; and by-and-by
we learn that in many cases this is really the surest sign
of their whereabouts.

We look at these little pellets of excrement, and gain at once
some idea of the size of the larvæ that produce them. Then we
observe whether they are fresh and moist, or dry and stale. If the
latter, it is not of much use to examine the leaves above; but if
otherwise, there is little doubt of our meeting with larvæ, as the
present position they occupy is so truly marked. The leaves just
over them are carefully examined, either by turning them over as
before described, or, if the height of the foliage admits of it,
by placing our heads below and looking upward.

If we find that the larvæ are some of those that endeavour to
escape by feigning death and allowing themselves to drop at the
slightest disturbance, the net is always kept beneath the leaves we
are touching in order to intercept them in their downward journey.

Continuing the search, we meet with leaves that are rolled up
and bound with silk threads, and others that are drawn together
and similarly bound. These are carefully uncurled and pulled
asunder with the result that active little larvæ are exposed to view,
or, it may be, pupæ are discovered. In some cases flowers are
drawn together in just the same way, and an examination reveals
one or more of the species that prefer petals and other parts of
flowers to the green leaves.[Pg 105]

Silken threads always arouse our suspicions. These may be seen
lying on the surfaces of leaves, and passing from one leaf to another,
or they may be hanging perpendicularly from the branches of trees
above. In the latter case a larva may be frequently seen on the
lower extremity of the fibre, swinging gently in the breeze, and,
should we require it, we have only to place the open box below for
its reception.

Hawthorn and other trees are sometimes seen almost devoid of
leaves, nearly every bit of green having been greedily devoured by
a host of small larvæ. In such cases we often meet with dense
clusters of silk fibres that may easily be mistaken for spiders’ nests.
But when we look more closely into the structure we observe that
we have discovered instead nests of gregarious larvæ, such a large
number being in each little community that the deplorable appearance
of the tree is at once explained.

A little farther on we meet with a sickly-looking plant in the
midst of a number of flourishing individuals of the same species,
and stop to make inquiries into the cause of this strange occurrence.
Is it due to a poorness of the soil? No, this cannot be the case;
for intermingled with its roots are those of its flourishing companions.
We pluck a stunted and half-shrivelled leaf and examine
it. At first we do not notice the cause of its peculiar condition;
but, holding it up to the light, and looking through it, we see a
number of little galleries that have been eaten out of its internal
soft substance, leaving the thin skin (epidermis) almost entirely
intact. But nothing more is to be seen. Another leaf is examined
in exactly the same way; and here we see the little destroyer, lying
motionless in its burrow till a gentle pressure applied against it
from outside causes it to wriggle along its narrow passage. This is
the larva of one of the little leaf miners mentioned again on
page 303.

Reaching a little marshy spot we see a number of water-loving
reeds, most of them beautifully green and in a flourishing condition,
but here and there in their midst is a poor stunted specimen—another
result of the ravages of the larvæ of one or more moths.
An examination of the blades reveals nothing; but on splitting
open the stalk we discover some larvæ that have already devoured
a quantity of the internal pith, and thus endangered the life of the
plant. On inspecting other similar reeds we are at first puzzled as
to how the larvæ could get inside the stems without damaging the
outer portion; but at last we see in each one a little discoloured[Pg 106]
hole that was eaten out by the young caterpillar just after its escape
from the egg. Once within the reed, it found a plentiful supply of
food, and there grew at the expense of the plant without doing any
further external damage save by causing a stunted growth.

It may be that the stem eaters we have found are just about
full grown. If so we examine a number of the stems with a hope
that we may find one or two that are just about to change to the
chrysalis state, or even a pupa already formed. By this means we
may secure one of the perfect insects without the necessity of feeding
larvæ at home. Such a consideration becomes a most important
one when it happens that the required food plant is one that cannot
be easily obtained.

Close by the reeds is another water-loving plant in the form of
an old willow tree. This is always an attractive object to the
entomologist, so it comes in for a share of our inspection. On its
leaves we may find several species of the larvæ of Lepidoptera,
including those of some of our largest insects. But a strange feature
catches our eyes as we happen to glance at the bark of the tree.
Here we see a few holes of different sizes, about which are a number
of little fragments of wood that remind us of ‘sawdust;’ and,
examining the ground below, we see quite a little heap of this
dust, looking just as if a carpenter had been at work on the spot.

This is not the effect of a saw, however; it is a sure sign of the
ravages of wood-eating larvæ (p. 224), whose powerful jaws gain
them admittance into the very hearts of trees, and the application
of the nose to one of the larger holes leaves no doubt of the presence
of the large and beautiful caterpillar of the Goat Moth
(p. 224).

If we require any of these wood-eaters, either for rearing or for
preservation, we must be prepared for a little rather heavy work.
A strong pocket knife is not sufficient, but with a good chisel the
wood can be gradually cut away, and the galleries traced, till at
last we come to the larvæ snugly resting in their burrows.

It often happens that the tree thus tenanted is half decayed, and
consequently the work is rendered much easier. Also, while tearing
away the wood, we often meet with a number of cocoons that
have been constructed by the caterpillars for their winter quarters,
or as a resting place while undergoing their transformations. These
are composed of the wood dust bound together by strong silk fibres,
and are often in such a good state of preservation that they form
useful illustrations for the cabinet.[Pg 107]

As further aids to larvæ searching we may mention that many
species—chiefly of the Noctuæ—hide under the surface of the ground
or among dense and low herbage during the day, and come out to
feed only by night; that many others feed on roots, and are therefore
seldom seen above the surface of the soil; also that a good
number burrow into fruits, in the interior of which they spend the
whole of their larval stage. The best way to secure the latter is to
examine the ‘windfalls’ that lie scattered on orchard lands, for it
is a well-known fact that the fruits that are infested with larvæ
generally fall earlier than others—a result that must be attributed
to the damaging work of the larvæ themselves.

All the larvæ collected should be carefully boxed at once, a
separate compartment being used for each species, and a few fragments
of the food plant being introduced in each case. It is also a
good plan to have each box previously lined with moss as a further
addition to the comfort of the captives. Without such a precaution
some of the more delicate species are liable to injury during their
transmission from field to home.

Hitherto we have obtained our larvæ by searching only, but
there are times and occasions when our boxes may be far more
rapidly filled by methods that are not such a tax on our time and
patience. Suppose, for instance, that we reach a bush, the mutilated
leaves of which seem to show that larvæ are present on its
branches. We spread our white cloth or open out the white-lined
umbrella just under a selected branch, and then tap that
branch very smartly with our stick.

Down comes a host of living creatures! Spiders, larvæ, beetles,
aphides, earwigs, and what not, struggling and running about on
our white fabric in all directions, and all mingled with bits of stick,
leaves, and fragments of all kinds. We leave the cloth or the umbrella,
as the case may be, quite still for a few seconds to allow all
the living creatures to get a good foothold, and then, raising it into
a vertical position, allow all the rubbish to drop off.

We can now put the cloth down again, and select as many of
the larvæ as we require, giving our first attention to the nimble
runners and loopers that are already near the edge and just on the
point of making their escape. This productive method of larva
hunting is known as ‘beating,’ and is particularly applicable to tall
herbs and the lower branches of trees and shrubs.

The same principle may be employed in the case of branches
that are quite out of the reach of the stick, but the blows are here[Pg 108]
applied to the trunk, a mallet or some other rather heavy implement
taking the place of the stick.

Another splendid method of securing larvæ where mere searching
would be tedious and unproductive, lies in the use of the sweep
net described on page 102. This implement comes into service in
waste places that are covered with rank vegetation, in clover and
hayfields, and in all spots covered with low herbs.

Walking among the vegetation, the net is swept right and left
before you, and the contents examined at frequent intervals. It is
advisable to work the different species of herbs separately as far as
possible, otherwise there may be some difficulty in the determination
of the food plants of the mixed larvæ that the net will
contain. If, however, this plan is impracticable, you may save
time by turning out all the ‘sweepings’ into one large box, leaving
the sorting to be done at home in leisure hours.

Collecting Pupæ

We have seen that ova and larvæ may be obtained in greater or
less abundance at all times of the year, so variable are the seasons
of the different butterflies and moths. The same remark applies
equally well to pupæ; but so many of the Lepidoptera spend the
winter months in the chrysalis state that this period may be
regarded as the harvest time of the pupa hunter.

A large number of caterpillars undergo their change to the
quiescent state during the months of August and September, and,
of course, remain in this state until the warm days of the following
spring or summer. And as insects even in the pupal stage have a
number of enemies and dangers to contend with, it is advisable to
start your search for them as soon as possible after they have
changed.

If you set your mind on searching for particular species, you
should endeavour to ascertain the usual time at which such species
pupate; make any necessary allowances for the forwardness or
backwardness of the season, and then allow a week or two for the
change to be completed, for insects should never be disturbed at
times when their metamorphoses are in progress.

For general pupa hunting the best season is undoubtedly from
the end of August to the end of October, but there is no reason
why the work should not be carried on throughout the winter. If,
however, you continue your work so late, you must not expect[Pg 109]
nearly as much success as time advances. You must remember
that entomologists are not the only pupa hunters. Many hungry
birds are always on the look-out for insects, and seem to enjoy
them equally well in all their stages. Those that hybernate on or
under the ground are liable to fall a prey to moles and beetles. In
addition to these dangers, all pupæ are subject to the effects of
extreme cold, dampness, or floods.

As regards the choice of a day, very little need be said. Any
day that is sufficiently genial for yourself will do for your work,
except that periods of hard frost render the ground too hard for
digging—the most profitable part of the pupa hunter’s task.

The apparatus required is extremely simple: A satchel or
large pockets full of small metal or chip boxes, a small garden
trowel, and a strong chisel.

If metal boxes are used they should be perforated; in fact,
nothing is better than the ordinary larva boxes of the dealers.
All the boxes, of whatever kind, should be lined with moss previous
to starting work.

The trowel and chisel do not pack well with a number of small
boxes, therefore it is a good plan to fix them in a couple of
leather sheaths attached to your belt. In this position they are far
more handy for use, and the boxes are also in less danger of being
crushed or damaged, as they probably would be if in contact with
hard and heavy tools.

A note book is also a valuable addition to your outfit, as it
enables you to make memoranda concerning the trees and localities
from which you obtain your pupæ.

The best localities for pupa hunting are clearings in woods,
parks with numerous large timber trees, and meadows in which
large isolated trees are scattered; and the best trees include willows,
poplars, oaks, beeches, birches, elms, and hawthorns.

The best thing you can do on arriving at the selected hunting
ground is to make at once for isolated trees of large size, and work
each one as follows:

First examine well the crevices of the bark, for many caterpillars
descend the tree to within a short distance of the ground,
and then seek out a snug little crevice in which to spend the
winter, often protecting themselves with silken cocoons, or constructing
a neat little shelter of gnawed fragments of the wood
cemented together.

If there is any loose bark, very carefully force it out with your[Pg 110]
chisel, and examine both its inner surface and the wood from which
it was removed. The wood thus exposed may reveal openings
of the galleries of wood-eating larvæ, in which case, unless the
material is too hard to be broken up with the chisel, you may be
able to trace out a few pupæ. Where these exist, they are usually
to be found very near the entrance, sometimes even protruding
slightly from the opening, for the larvæ generally place themselves
in this position of easy escape when about to change.

Next give your attention to the moss, if any, covering the lower
portion of the trunk. This affords a very favourite shelter to
many species. Tear it off very carefully, beginning at the top, and
watch for loose pupæ and cocoons as you do so. Then hold the
clumps you have removed over a patch of bare ground or over a
spread handkerchief, and pull it to pieces, in order that any pupæ
it contains may fall out; also examine the fragments carefully for
others that may remain attached.

This done, the surface of the ground must be examined.
Remove all dead leaves, and watch for pupæ that may be sheltered
beneath them. If any loose stones lie on the ground, turn them
over. Search well into the angles between the roots, and if there
are any holes or hollows beneath them or in the trunk itself, pull
out all loose matter within, and feel gently above and around for
cocoons.

After all loose matter has been removed, there still remains the
soil for examination. If this is very hard and clayey, it is probably
useless to carry the search any farther; also if very wet you
need not expect much; but if comparatively dry and friable there
are more hopes of success.

As a general rule the north and east sides of the trunk are
drier than those which are exposed to the heavy rains brought
by the south and south-west winds, and are consequently more
favoured by larvæ that are seeking a resting place for the winter.

Most larvæ seek shelter in the angles between the roots of the
trees on which they fed, but a few species seem to prefer the
edges rather than the corners; and in cases where no such angles
are formed at the surface, you will do well to examine the earth
and turf all round the trunk; but it is generally useless to extend
the search more than a few inches from the tree.

After having searched every available nook and corner as far
as possible without digging, thrust the trowel obliquely into the
soil a few inches from the tree, turn over the sod, and then examine[Pg 111]
the spot from which it was removed. Now give your attention
to the sod itself. If loose and friable, break it up gently,
keeping a sharp eye for falling pupæ, and also for earthen cocoons
that are easily mistaken for little lumps of soil.

If the soil is held together by roots, it must be pulled to pieces,
and the fragments shaken over a bare piece of ground where the
fall of a pupa or cocoon could be easily seen; and if you have
removed a grassy turf, it will be necessary to look between the bases
of the blades as well as among the roots.

In this way you may search round tree after tree, wherever the
soil is of such a character as to allow of the admittance and shelter
of larvæ. But the variability of your success will be quite beyond
your comprehension. Sometimes you will sight a grand old oak
with the most favourable anticipations, and consider yourself quite
certain of a good find when you discover, on a nearer approach,
the liberal coating of moss that clothes its trunk and the dry sandy
soil at its foot; and yet the most careful search ends in nothing
but disappointment. At other times you try your luck at tree
after tree without ever seeing a single pupa or even a cast-off case,
and then, when just on the point of despairing, you search round
another that is apparently much less promising, and, to your great
surprise and delight, a dozen or two are turned out in a few minutes.
Such an occurrence as this is not at all uncommon, and cannot be
satisfactorily explained, but we must take things as they come and
make the best of them, remembering that pupa searching is one of
the best of all entomological operations wherewith to test one’s
perseverance and patience.

It may be mentioned, in conclusion, that the pupæ of Lepidoptera
are never to be found far below the surface of the soil. Generally
they exist, if buried at all, only an inch or two down, and very
rarely at a greater depth than four inches.

In our next chapter we shall learn how to rear the perfect
insects from the earlier stages we have been considering.


[Pg 112]

CHAPTER VIII

REARING LEPIDOPTERA

Management of Ova

In the management of insects in all stages the strictest attention
must always be paid to one general rule on which the success of
the work almost entirely depends; and that is—keep every specimen
as far as possible under the same conditions as those in which you
find it in nature.

Applying this principle to ova, we store them in airy and light
places, protected from the direct rays of the sun, and avoid handling
and rough treatment of any kind. It is also advisable in most
cases to maintain a slight amount of dampness corresponding with
that of the open air at the particular season of the year.

They do not require much space, and it is certainly desirable
not to give much, otherwise the newly hatched larvæ, when their
time arrives, will actively wander all round their premises in search
of food, and give you no end of trouble in gathering them up.

Chip boxes are, as a rule, very good and very convenient
receptacles for ova. After placing the eggs in these, cover them
over with very fine muslin, held in place by elastic bands; and label
each as far as you can with the name of the species contained, and
other particulars worth remembering. The boxes may then be
put in front of a window facing north, or in any situation within
or out of doors where rain and sun cannot reach them. A greenhouse
is an admirable place in which to keep them, the natural
dampness of the atmosphere being apparently a considerable
assistance to the tiny larvæ just as they are striving to escape from
their shell.

Whatever place is selected, it is absolutely necessary that the
ova be carefully watched, so that each brood may be supplied with
the required food plant within a few hours of quitting the shells.[Pg 113]

When ova are kept in a warm room, very great inconvenience
and even loss is sometimes caused by the appearance of larvæ before
the necessary food plant shows its buds. Yet, on the other hand,
it is sometimes a great gain to the entomologist to get certain
broods off early in the season, providing the food is at hand; for
in this way he can not only get some of his work over during a
slack season, but also, if he desires it, secure an additional brood;
that is, one brood more than the usual number. Thus, supposing
a certain species he is rearing is naturally double-brooded, he can,
by judicious management, secure three successive broods before the
food plant casts its last leaves.

This hastening of the natural events of insect life is known as
forcing, and merely consists in subjecting the species concerned to
a reasonable amount of artificial heat, such as that of a room in
which a fire is always kept, or of a hothouse.

It is interesting at all times to note the dates on which eggs are
laid or collected, and the times at which the young larvæ appear.
In addition to this all changes that take place in the colours or
forms of eggs should be carefully observed; for such changes will
assist you in distinguishing between fertile and sterile ova, and
also enable you to judge approximately as to the date of the
appearance of future broods.

Rearing Larvæ

The main point in connection with the rearing of larvæ is certainly
the selection and construction of the cages or their substitutes.
For newly hatched and all very small caterpillars a small bottle
with a wide mouth makes a very fair abode. Put a layer of sand
or sifted soil in the bottom, fix in this a small twig of the food plant
or lay a few leaves on the top, and then, after the larvæ have been
introduced, cover the top with a piece of muslin, held in place by an
elastic band.

The great drawback with this arrangement is the lack of any
provision for keeping the food moist and fresh, thus rendering a
change necessary at very frequent intervals; but this may be
obviated by using damp sand as a foundation for the little twig
of food plant. With this improvement, if you cover the top of the
bottle with apiece of glass, a saucer, or any impermeable substance,
you may keep the twig fresh for several days, generally until the
disappearance of the last leaf calls for a fresh supply; but it is[Pg 114]
very doubtful whether the damp atmosphere resulting from this
inclosure is not injurious to the larvæ. It certainly does not seem
to have much influence on some, but the unhealthy conditions that
result must be detrimental to the inmates. It must also be remembered
that many species require a dry soil in which to burrow
when about to change.

When the time comes for the change of food, great care must be
taken not to injure young and small larvæ. In many cases they
need never be touched, for if a fresh twig be placed beside the stale
one, they will readily find their way to it; and to facilitate this, and
also to afford a convenient foothold to those larvæ that accidentally
fall from the twig, the layer of sand at the bottom of the bottle
should be covered with moss or cocoa-nut fibre.


Fig. 57.—A Larva Glass.


Fig. 58.—A Larva Glass.

If you find it necessary to
move the larvæ yourself from
the stale food, never touch
them with your fingers, but lift them gently by means of a small
camel-hair brush. Larger larvæ need never be moved at all. They
will always search out fresh food for themselves, and the stale may
be removed after they have quitted it.

For rearing larger species ordinary bottles are hardly satisfactory,
and we must either use large jars or construct cages of some kind.

An ordinary bell jar such as is used for covering ferns or for
aquaria makes a very useful ‘larva glass.’ Place a small bottle of
water at the bottom, and then introduce sufficient dry clean sand or
sifted soil to reach up to its neck. On the top of this place a layer
of moss or cocoa-nut fibre. Next introduce the food plant, fixing it
firmly in the bottle of water, and plugging up the space between[Pg 115]
the stem and the rim with cotton wool. This precaution is to
prevent the larvæ from falling into the water as they attempt to
pass up or down the stem, and the wool also helps to keep the
twig in a vertical position. The glass is now ready for the caterpillars,
but it is advisable to keep a covering of muslin or gauze
over the top in all cases even though the larvæ contained are unable
to creep up the surface of glass, for the great enemies of caterpillars—the
ichneumon flies—are always on the alert, and will often take
advantage of an open window to ‘sting’ the larva rearer’s pets.

Another form of larva glass can easily be made out of a large
glass jar if you know how to cut off the bottom, or of a chemist’s bell
jar which is open both at top and bottom. In this case the bottle
of water and the soil are arranged as
before in a pan of unglazed earthenware,
and then covered over with the
glass. This is shown in fig. 58, and is
an exceedingly convenient larva house,
since the lifting of the glass enables
you to get at the insects without any
trouble.


Fig. 59.—A Larva Cage.

Wood larva cages are very commonly
used for the larger species after
they have attained a fair size and require
more food than can be stocked
in bottles and glasses. These cages
have glass fronts, either sliding or in
the form of a hinged door, and sides
of perforated zinc. They are kept in
stock by all dealers in entomologists’ requisites, but equally useful
ones are easily constructed. If you select a box of suitable size at
the grocer’s, cut out large pieces from the lid and sides with a fret
saw, and fix in the glass and zinc, you will have a cage that will
answer all purposes.

The internal arrangements consist of a shallow tray filled with
soil, in which stands the bottle of water for the food, and a layer of
moss sufficiently high to cover the bottle completely.

A series of such boxes standing on end on a shelf, or hanging on
a wall, will form a very satisfactory nursery for your pets, and will
occupy but little space.

We have already observed that some larvæ burrow into soil
when about to change, while others creep to a sheltered corner, or[Pg 116]
suspend themselves from the food plant itself. It will be seen that the
larva cage just described supplies all these demands, and care must be
taken not to disturb the occupants while they are undergoing their
metamorphoses. Those that suspend themselves on the food plant
should be allowed to remain where they have fixed themselves, and
when it is necessary to remove the stale food in order to give a fresh
supply to the later larvæ, let it be fixed in an airy place where it can
be watched till the perfect insects emerge. Those which suspend
themselves on the sides or top of the cage, or spin cocoons in the
corners, should never be disturbed unless you are greatly in want of
the same cage for the accommodation of another brood; and even
then it is possible that their presence will not in any way interfere
with the new species. But if their removal becomes a necessity, let
it be carried out as carefully as possible, and not until the change
to the pupal stage is known to be complete.

The species that burrow into the soil or bury themselves in the
moss need never be disturbed till the rearing season is quite over,
and then they may be transferred to a box specially kept for the
accommodation of pupæ.

There is yet another method of rearing larvæ to which we must
refer—a method known as ‘sleeving’—particularly useful when
you happen to have the required food plants in your own garden.
The ova or larvæ are placed on the plant, the whole or part of
which is then covered with a bag or ‘sleeve’ of gauze. The larvæ
thus imprisoned have the full benefit of fresh air and light, and
are also free from the attacks of ichneumon flies. They have a
fair amount of liberty, and yet cannot get beyond your reach;
also abundance of fresh food without further trouble on the part of
the rearer.

But even this arrangement is not perfection. It will not suit
the night feeders that like to hide beneath the soil during the day,
and it interferes somewhat with the burrowing tendencies of those
which pupate underground. These little difficulties, however, can
be overcome by placing the food plants in large pots or tubs of
soil, and tying the mouth of the ‘sleeve’ round the outside of this
utensil. If this cannot be done, those insects that pupate underground
must be removed from the plant when their restless
disposition shows that the changing time has arrived, and then be
transferred to a box of soil where they can find the seclusion they
seek.

The larvæ that hybernate throughout the winter are rather[Pg 117]
more troublesome, especially those which are inclined to take a
ramble on certain mild days in search of food when none is at
hand. Still there is no reason why even a beginner should not
attempt the rearing of these. They will require food in the
autumn until the cold weather sets in, and again early in spring
as soon as the new leaves appear; but this is not of much
consequence to those who reside in districts where the required
food plants abound.

Wood feeders also require some special treatment and precautions,
and the successful rearing of some is a matter of no little
difficulty. A wooden cage is, of course, quite out of the question
with these, unless you wish to test the power of their jaws. They
must be kept in large pots or jars, covered over with wire gauze or
perforated zinc, and supplied with fresh stems or logs of wood, or
with moist sawdust fresh from their favourite tree. A few of them—the
‘Goat’ (page 224), for example—will eat dead and rotting
wood, and may be fed on old palings and other waste providing the
right kind is selected.

The troubles and disappointments of larva rearers are numerous
and varied, and commence with the earliest moments of the
young insects. Even the hatching period sometimes proves a
trial, for it occasionally happens that the young larva has not
sufficient strength to bite its way through the shell that surrounds
it, and dies with nothing but the surface of its head exposed to
view. This may be the result of keeping the ova in too dry a spot,
the shell having become too hard and horny for the little creature’s
jaws.

Then the moulting seasons are always periods of trial to the
larvæ, and often of loss to the rearer. Some of the hardier species
may pass through all their moults without appearing to suffer anything
more than a slight inconvenience at each, but in other cases
the greater part of a brood may fall victims to these ailments of
the growing stage.

Apart from these sources of loss, however, larvæ are subject to
numerous diseases, infectious and otherwise, about which we know
but little. A fever may rage in one of our cages; a fungoid growth
may establish itself on the bodies of our pets, or we may see them
cut down, one by one, through a fatal attack of diarrhœa.

In many such cases we are at a loss as to what to do. Blue
pills and black draughts are not to be prescribed, and the modern
practices of surgery and inoculation have not yet been applied to[Pg 118]
insect patients with very great success; but we must do our best
to adopt hygienic principles, paying the greatest attention to
proper means of ventilation and to a regular and wholesome dieting.
In the case of diarrhœa—a very common insect malady—the
best we can do is to avoid the young and juicy leaves of the food
plant, and substitute the older, and drier foliage.

Ichneumon flies have already been mentioned as great enemies
of larvæ. These flies either deposit their eggs on the skins of
caterpillars, or thrust their sharp ovipositors into the creature’s
flesh and lay their eggs beneath the skin. When the young
ichneumons are hatched, they immediately begin to feed on the
fatty matter that is usually stored in comparative abundance under
the skin of the caterpillar, and thus they grow at the expense of
their host, within whose body they lie completely hidden from
view.

The poor caterpillar, though being eaten alive, often shows no
external signs of the mischief wrought within, and, even though
its substance is really decreased by the hungry internal parasites,
yet the rapid growth of these robbers maintains the general plumpness
of a healthy larva. But the ichneumons, having at last
devoured the store of fat, and avoided the vital organs of the
caterpillar, as if with a view to preserve their living home to the
latest moment, now commence to attack the latter, speedily
reducing the vitality of their host to the lowest ebb, and finally
causing its death.

This untimely end may come before the caterpillar is full grown,
or the insect may change to the pupa before the ichneumons have
done their worst, but it rarely occurs that the unfortunate creature
has sufficient strength to carry it on to the final stage.

A large number of the collected larvæ will have been ‘stung,’
much to the disgust and disappointment of the rearer; and hence
the advantage of rearing your specimens from ova wherever possible,
providing you keep them so well under cover that the ichneumons
cannot visit your broods.

The Management of Pupæ

The disappointments connected with the rearing of Lepidoptera
are by no means at an end when all have passed successfully into
the pupal condition, and the number of perfect insects obtained
will often fall far short of the number of pupæ in your boxes; but[Pg 119]
we must now see what can be done to minimise the death rate of
the captives.

One or more suitable boxes must be prepared for the reception
of the pupæ, and the following suggestion will answer all
purposes:

Get a wooden box, quite rough and unplaned inside, large enough
to accommodate your pupæ with ease, and not less than eight
inches deep. Make several holes in the bottom, or else knock the
bottom completely out, and nail in its place a sheet of perforated
zinc. Also make a lid consisting of gauze attached to a light wood
frame.

Place a layer of clean gravel, about an inch deep, in the bottom,
and over this a few inches of sifted soil or cocoa-nut fibre.

Now take all the pupæ that are ‘earthed’ in your cages, and
arrange them on the prepared bed; also add to them the pupæ
you may have dug out during your various excursions. Cover all
with a layer of the material selected for the bed, and then add a
layer of moss.

Next come the pupæ that are suspended by silky fibres, or are
inclosed in cocoons. These should be fixed with pins around
the sides of the box, running the pins either through the tuft of
silk at the ‘tail,’ or the outer layer of the cocoon, or through the
portion of the dried food plant to which they are attached.

Here your pupæ will remain till they emerge, and the box may
be kept in any airy place where it is not likely to be forgotten, for
it is essential that the perfect insects should be removed as soon
as possible after quitting their cases. It does not matter much
whether the pupæ be kept in or out of doors, providing they are
sheltered from rain and very severe frosts; but of course, if the
former, the imagines will emerge a little earlier, even if the room
in which your specimens are stored has no fire.

Even when protected in boxes such as that described the pupæ
are subject to enemies and dangers. The soil and moss employed
may contain slugs, mites, or other creatures which prey on insects,
and the amount of moisture present in these materials and in the
atmosphere may prove too little for some species or too much for
others.

The remedy for the former evil is a simple one. Bake the soil
or fibre well before fitting up the box, and boil and afterwards dry
the moss. You may then be sure that all life previously contained
is quite destroyed.[Pg 120]

But the degree of humidity is a point not so easily settled, and
so variable are the experiences and opinions of different entomologists
that it is difficult to advise a beginner on the subject. The
fact that some strongly advise a perennial dampness, while others
recommend no attempt at the application of water, would seem
to show that there are probably important points to be urged on
both sides.

Nothing can be better than a very careful observation of pupæ
in their natural conditions. When engaged in pupa digging you
will observe that the larger number are to be found on the east and
north sides of trees where the soil is protected from the heaviest
rains; on the other hand a good many are certainly found in very
moist and sometimes even in wet situations.

Particular notice should be taken of such experiences, making
every allowance for the exceptions that prove the rule, and then let
the natural conditions be maintained in your nurseries at home.
To carry this out two pupa boxes should be kept, one for those
species that seem to require dry situations, and the other for the
species that apparently do best with moist surroundings.

But when it is desired to maintain the pupæ in a moist condition,
great care must be taken not to allow any accumulation of
stagnant water. The box we have described, with its bottom of
perforated zinc, is well adapted for this purpose. Let it stand on
a couple of strips of wood, so that any excess of moisture may
readily drain through. The perforated bottom will also allow of a
free circulation of air, thus securing the ventilation that is desirable
in all boxes, whether wet or dry.

If you have any insects that have pupated within moist stems,
they should be kept in a moist condition till they emerge. The
simplest way of doing this is to support the stems in a layer of
wetted but well-drained silver sand.

Forcing may be resorted to when it is required to obtain the
imagines for early setting in order to get them in the cabinet before
the busy season begins. The method is simple. Place the pupa
box on a shelf in a room where a fire is kept every day. By this
means you may get all your specimens out within a few weeks,
even when you start the forcing at the beginning or middle of the
winter. If, however, you require the imagines for breeding, you
must be careful that the eggs are not laid long before the buds of
the necessary food plants are due.

When you are expecting the appearance of perfect insects, the[Pg 121]
pupa boxes should be examined every day. A morning visit to
your pupæ (for most insects emerge in the morning) may reward
you with the sight of a newly emerged imago, clinging to the
rough surface of the box, thus affording you an opportunity of
observing the wonderful expansion of the wings. But the greeting
is not always of such a pleasant character, for your disappointed
eyes will sometimes be cast on a host of horrid ichneumons that
have just quitted a shell from which you were expecting a prize
of some specially valued species.


[Pg 122]

CHAPTER IX

SETTING AND PRESERVING

Setting and Preserving Butterflies and Moths

Up to the present we have been dealing only with living forms—learning
how to catch and rear the Lepidoptera that fall to our
lot; but now we have to become acquainted with the methods of
preparing our dead specimens in such a way that they may form a
useful collection for future study and reference. Our first attention
shall be given to the apparatus necessary for this work.

The most important requirement is the setting boards, of which
several are necessary, the sizes varying according to the dimensions
of the different insects to be ‘set.’ The lengths of all the boards
should be the same, not only for the convenience of packing when
not in use, but also in order that they may, if required, be arranged
neatly in the ‘drying house’ to be presently described. The widths
only will vary, and in this respect the boards must be adapted
to the measurements of the insects from tip to tip when the
wings are fully expanded. Thus, a set of a dozen boards, ten
or twelve inches long, and from one to five inches wide, will do
for a good start. Of course you may commence with a smaller
number than twelve, but if you really mean to do the thing well,
you will eventually require a good stock of boards.

Here, again, it may be mentioned that all the necessary requisites
may be purchased ready for use, a set of boards and a drying
house complete costing from ten to twenty shillings according to
size and quality; but as the reader, like myself, may prefer to construct
his own, I will supply him with hints and suggestions sufficient
for the work.

Each board is constructed in this way. Cut out and plane up
a piece of wood of the required length and breadth, and about one-eighth
of an inch thick. Glue on the top of this a layer of cork[Pg 123]
about half an inch in thickness, leaving the whole under a moderate
pressure until the glue is quite hard. The sheets of cork for this
purpose may be bought at any naturalist’s stores; but slices cut
from good large bottle corks may be made to answer equally well
if you don’t mind the extra time expended in cutting and fixing.

When the glue has well set, trim off the edges of the cork flush
with the sides of the wood,
and then cut out a groove
down the whole length of
the cork, of course in the
middle, and of such a size
that it will just contain
the bodies of the insects for which it is intended.



Fig. 60.—Section of a Setting Board.

The satisfactory cutting of this groove is not a very easy matter,
but if its position is first carefully marked, a long rat-tail file may
be made to plough it out neatly and regularly. As an alternative
the following plan is good. First cover the wood with a layer of
cork about a quarter of an inch thick, and then glue on the top of
this two narrower strips, about as thick as the bodies of the insects
for which the board is intended,
leaving a space of the required
size between them, as shown in
fig. 60. In this way you get a
groove of square section, that is
in some respects preferable to
the round one cut out by means
of the rat-tail file.


Fig. 61.—Sections of Setting
Boards.

Now comes a question about
which there is a difference in the
tastes or fancies of entomologists.
Shall the boards be perfectly
flat on the top, or shall the sides
slope from the groove, or shall
the surface be rounded? A
glance at the three sections of
setting boards will show clearly what is meant. The rounded board
is most commonly used, and the graceful curve thus given to a
butterfly or moth set on such is certainly attractive; but it is not
natural. The wings of these insects are rigid, and are never seen
bent into such curves in a living specimen. For this reason I
much prefer a perfectly plane surface on each side of the groove.[Pg 124]
Then, as to whether there shall be a slope or not, this is a matter
of less importance. A very decided sloping of the wings is certainly
not so convenient for future examination; nor does it, to my mind,
look nearly so well as both sides in the same plane, or at a very
gentle inclination. But perhaps this subject had better be left to
the taste of the reader, remembering, however, that, whatever plan
be adopted, all the boards should be alike in this respect, so that
there may be a degree of uniformity in the cabinet.

The surface of the cork must, in all cases, be nicely smoothed
down with glass paper, and then covered with thin white paper,
fixed to its surface with ordinary paste.

When insects are on the boards, they should be placed in an
airy spot, as free as possible from dust, while they are drying.
Hence the advisability of some form of ‘drying house.’ This is
simply a box, standing on end,
and provided with a hinged door
consisting of a sheet of perforated
zinc in a wooden frame.
The boards may slide in this on
little slips of wood nailed or
glued on to the sides, or the
wooden bases of the boards may
project beyond the cork at the
ends, and slide into grooves in
the side of the house.


Fig. 62.—A Butterfly on the
Setting Board.

Beyond these requirements
nothing is wanted save a good
stock of pins, thin card or ordinary
writing paper, and a ‘setting needle.’ The last-named item
is simply a needle mounted in a handle, and a good one may be
made by thrusting the head of a darning needle into a piece of twig.
The pins used for setting—that is, for fixing the pieces of paper or
card to keep the parts in position—may be of the ordinary kind;
but entomological pins are far preferable, even for this purpose;
for, being much thinner, they do not damage and disfigure the
setting boards so much.

Now as to the setting. First see that the pin with which you
are to fix your dead insect passes centrally through the thorax.
Then fix it firmly on the setting board, its body lying neatly in the
groove of the cork. Cut out some little pointed strips of card or
paper, and, after bringing the wings into position with the setting[Pg 125]
needle, fix each one by a pinned strip. In spreading out the wings,
care must be taken not to pierce them at all, but simply to push
them into their place by pressing the needle at their bases, or by
putting the needle beneath and lifting them out.

Instead of pointed pieces of card, uniform strips of paper may
be used, as shown in fig. 63, each strip passing over both wings.

After the four wings have been properly arranged, a few extra
pins may be used to keep other parts in position. Thus, the
antennæ may be placed at equal angles, the proboscis may be extended,
and a couple of pins may be used to support the abdomen
if it is inclined to bend downward.



Fig. 63.—Another Method of Setting
Butterflies and Moths.

As before mentioned,
insects should
be set soon after they
are dead, while the
parts are still soft and
supple. But where
this cannot be done,
and the specimens have
become stiff, brittle,
and rigid, they must be
‘relaxed’ before any
attempt is made at
setting them out.

This process of relaxing
consists in placing
the specimens in a
very moist atmosphere
for a few days. There
are several simple
ways of doing this, many of which will readily suggest themselves
to the reader. Your collecting box, if a zinc one, may also be
used as a relaxer. Pin your stiff insects in it, after well moistening
the cork, and simply shut them up for a day or two. Any metal box
will serve the same purpose providing you put into it a piece of
sheet cork on which to fix the insects, and this cork may rest on a
bed of moist sand.

Another plan is to float the pinned specimens on corks in a
shallow vessel of water, and cover them over with a bell glass.

Insects that are being relaxed should be examined from time
to time, and the degree of flexibility acquired tested by a gentle[Pg 126]
pressure of the setting needle or by blowing on them. If not
sufficiently supple, give another day in the damp cell, but never
allow them to be forgotten till they are covered with mildew.

The time occupied in thoroughly drying butterflies and moths
will vary considerably according to their sizes and the condition of
the atmosphere. In hot and dry summer weather four or five days
will prove quite sufficient for the very small and thin-bodied species.
From one to two weeks, however, may be looked upon as the
average period; but the large and thick-bodied moths may require
more than this.

Perhaps the best test of their condition is the gentle pressing of
the setting needle against the abdomen—the last part of the body
to become dry and stiff. If the abdomen seems quite firm and
rigid, you are pretty safe in removing the specimen from the
board; but if it bends at all under a slight pressure of the needle
let it remain for a day or two longer.

If your cabinet is quite ready for the reception of new-comers,
the insects may be put in their proper places immediately after
their removal from the setting boards; but if not, they may
be pinned temporarily in a ‘store box’ till the time comes when
you have proper accommodation provided. The full consideration
of these matters will be dealt with in another chapter.

It is possible that the setting of some of your specimens will not
exactly please you. If such is the case, put them in a relaxing box
for a day or two, and then reset them more to your fancy.

We have now to deal with a matter that applies more
particularly to moths, especially the very large and thick-bodied
species. The abdomens of these become more or less contracted
and shrivelled on drying, sometimes to such an extent as to look
most unsightly.

There is a remedy for this, and the time and patience required
in working it out will be well repaid by the superior results
obtained.

While the abdomen is still in a soft condition, make a slit
throughout its length with a very sharp knife or a sharp-pointed
pair of scissors. This slit should be made down the centre of the
under surface, or, if the insect is to be placed in the cabinet with
the under side exposed, down the middle line of the back. Then
remove all the contents of the abdomen, scraping them out with a
piece of hooked wire, or removing them with a fine pair of forceps,
and leaving the skin as clean as possible both within and without.[Pg 127]
Now introduce a packing of cotton wool, just sufficient in quantity
to maintain the natural form of the body as the specimen
dries.

There is another good method of stuffing moths that possesses
a decided advantage over the one just described, since it leaves the
specimen in such a perfect condition that it shows no appearance
of having been stuffed when viewed from either side. This consists
in snipping off the abdomen at the waist, clearing out the contents
with a hooked wire, lightly stuffing it with cotton wool pushed in
at the waist, and then setting it aside to dry, while the other part
of the insect is undergoing the same process on the setting board.
When both parts of the moth are thoroughly dry, the stuffed
abdomen is easily fixed in its place with a little coaguline; and this,
if neatly done, will not show the slightest sign of the treatment to
which the insect has been submitted.

Even after your insects are finally housed in the cabinet, they
are subject to two other dangers, both of which are more destructive
to moths than to butterflies. One is technically known
as ‘grease,’ and the other is the invasion of certain museum pests
that feed on the specimens, causing them to fall to pieces.

Examine the moths that have been for a time in the cabinet,
and some are sure to exhibit an oily or greasy appearance, the hairs
of the abdomen, and perhaps also of the thorax, being clogged
together just as if the specimen had been dipped in oil, the
same miserable condition perhaps being shared also by parts of
the wings.

This is due to the gradual oozing out of the fatty matter that
is always present to a greater or less extent in the bodies of the
insects, and which must necessarily show itself more sparingly in
specimens that have been carefully stuffed.

The old saying, ‘Prevention is better than cure,’ applies well in
the present case; but as there are times when a knowledge of the
‘cure’ is the only means of saving a valuable specimen from
destruction, we will study both.

To deal with the two in the order of the well-worn proverb, we
will consider the prevention first. Always carefully clean out and
stuff the abdomens of large-bodied insects; and as a rule, treat them
with some substance that will either absorb or dissolve out all oily
matter. I think the best plan is to remove the abdomen, clean it
out if its size permits of such an operation, and then, after labelling
it to prevent its future application to the wrong body, either let it[Pg 128]
remain in a bottle of magnesia for several weeks, or soak it in benzole
or ether for a few hours or longer.

If magnesia has been employed as an absorbent, you have
simply to blow or lightly brush off the loose powder that clings to the
body, and then fix it in its place with coaguline. A body dipped in
ether or benzole will look as if completely spoilt at first, for the furry
coat that clothes it will lie matted and almost entirely robbed of its
beautiful colours, reminding one forcibly of the proverbial ‘drowned
rat.’ But take no notice of this change. Let the body have at
least a few hours in the liquid, extending the time to a day or two
in the case of very large ones and those which experience has
proved to be particularly liable to ‘grease;’ and, immediately on
withdrawing it, fix it with a pin in a good strong draught, such as
you may obtain by opening a window about an inch, or, if a breezy
day, in the open air.

These liquids are so volatile (and for that reason should never
be left exposed in an open vessel) that they rapidly evaporate,
leaving the dry hair to be loosened by the breeze, thus bringing
back the natural appearance almost perfectly.

It is probable that many of the smaller insects that were not
considered to require the stuffing or grease-removing operations
will sooner or later exhibit a greasy tendency in the cabinet. At
first the abdomen is affected, and the oily matter then gradually
creeps over the rest of the body, finally spreading over the wings,
and giving the insect a most deplorable aspect. But these are not
irreparably lost, and the following cure will often bring them back
to their former beauty.

If the abdomen only shows signs of grease, cut it off and soak
it in one of the above-named liquids for a day or so, replacing it as
above after the drying operation. If, however, the oily matter
has spread to the thorax and the bases of the wings, the whole
specimen must be soaked, using a basin or jar of suitable size,
covered with a plate of glass. A good draught during the drying
operation will do much to prevent the hair from sticking in matted
tufts close against the surface of the body and wings, and a gentle
brushing with a very soft camel-hair brush will loosen and reset
the fur.

The other danger to which we have referred is the invasion of
certain ‘mites’ and other museum pests that pay periodical visits
to our cabinet drawers and store boxes, often committing such
havoc as to severely try the patience of an interested naturalist.[Pg 129]

The way to prevent such intrusions is to make the atmosphere
of the compartments so obnoxious (to them) that they dare not
enter; and, further, to so spice up your specimens that they are
no longer safely edible to the invaders.

The first object can be attained by always keeping camphor or
naphthaline (albo-carbon) in each division. A lump of either substance
may be secured by pins or a little perforated cell in the
corner of each drawer or box, or the bottom of each may be dusted
with finely powdered naphthaline; but as both these solids are
volatile, care must be taken to renew the supply as occasion
requires.

Then, with regard to the second precaution, perhaps nothing
is more effectual than corrosive sublimate. A little of this may be
dissolved in a small bottle of alcohol (spirits of wine), labelled with
the name and the word Poison, and kept ready for use. All the
skins of stuffed specimens should be painted with this solution, and
the stuffing itself may be moistened with it before insertion.

There is yet another circumstance that renders a watchful care
of your cabinet specimens necessary, if you happen to possess
many that were captured ‘at sugar.’ Some of these will have so
gorged themselves with syrup that they are literally full of it, and
this will sometimes find its way to the outside, often dropping on
the surface beneath. In such cases the sugar should be removed
as completely as possible, and the bodies stuffed, before they are
quite dry; but if the specimens have been in the cabinet so long
that they are stiff and hard, the under sides of the abdomens may
be completely cut out with a very sharp knife and thrown away,
and then the sugar cleaned out from the upper shell as neatly as
possible.


[Pg 130]

CHAPTER X

PRESERVING OVA, LARVÆ AND PUPÆ

Many young entomologists give their attention almost solely to the
perfect forms of insects, often collecting and studying a very large
number of species without regard to their earlier stages and metamorphoses.
This is decidedly a very great mistake. Although
the lifeless form pinned in a cabinet may be a most beautiful object
in itself, yet a study of this alone is uninteresting compared with
that of the wonderful changes it has undergone since the time it
was a very young larva.

The different stages of the insects should be known as far as
possible, and these, as well as the perfect forms, should be included
in the collection for future study and reference. A good cabinet,
according to my own opinion, is one that possesses, among other
good features, a number of complete sets illustrative of the life
history of at least the more typical forms; and as it is not a
difficult matter to preserve the earlier stages, there is really no
excuse for their omission from the collection.

The empty shells of ova are in themselves sometimes interesting
objects, especially when they illustrate some peculiar instinct
on the part of the parent. Sterile eggs, also, often fall into the
hands of breeders and rearers, and these, though in other respects
unprofitable, are useful in the cabinet.

If fertile eggs are to be prepared for a collection, they must be
killed. This is easily done by thrusting into each one the point of
a very fine needle, or by immersing them for a moment in boiling
water, or by shutting them up in a bottle with camphor. In drying
they often contract more or less, and frequently change their
colour; still these are useful, providing notes have been taken of
the characters thus lost. The larger eggs are capable of special
treatment where the owner has the necessary time and patience,
and where the highest results are desired. By means of a surgeon’s[Pg 131]
injector of small size the contents of the eggs can be removed; and
then, by the same instrument, a warm solution of gelatine, coloured
in such a way as to restore the natural tint, may be forced into the
empty shell. As the gelatine cools and hardens, it prevents any
shrinking of the shell, and thus both form and colour are well
preserved.

For the preservation of larvæ you will require one or two
simple appliances.

The first of these is a suitable glass blowpipe, one form of which
is here illustrated. It consists of a glass tube, one end of which
has been drawn out very fine; a piece of watch spring tied to it in
such a manner that it will hold the skin of a larva at the small end,
and a piece of india-rubber tubing at the other end, pressed by
means of a brass spring clip.


Fig. 64.—A Blowpipe for Larvæ.

A little drying oven is also very useful, but not absolutely necessary.
If you decide to have one, any square box of sheet iron (not
soldered tinned iron) may be readily converted into one. It must
be provided with a hinged door in the front with a ventilator at the
bottom, a hole for the escape of hot air at the top, and a tripod wire
stand inside on which to rest the specimens while drying. The
whole should be supported on a wire stand, so that heat may be
applied below.

Each larva to be preserved should be dealt with in this way.
First kill it by means of any one of the killing bottles or boxes already
described, or by immersion in spirit of wine. When quite dead,
enlarge the anal orifice by thrusting a needle into it, and then lay
it on a piece of blotting paper with its head toward you. Now
take a round ruler, previously covered with blotting paper, and roll
the larva gently from head to tail till all the contents of the skin
have been expelled. Next fix the skin on the fine end of the blowpipe,
by thrusting the point of the latter into the opening, and
allowing the spring to press gently on its edge. Gently blow into
the skin till it is inflated just to a little below natural size, then[Pg 132]
either hold it near a fire or rest it in the drying oven till it is quite
dry and rigid.

If you have done your work neatly, the skin and blowpipe will
both be quite air-tight when the clip is closed; and the air, finding
no outlet, will still further inflate the skin when it expands on
exposure to heat. This is the reason why you are directed to blow
it out to something short of the natural dimensions. If you find
that this expansion causes the skin to stretch beyond its normal
size, a little of the air must be allowed to escape while it is yet soft
and flexible.

The front of the larva is generally the last portion to become
dry, and when this is quite rigid the skin may be removed from
the blowpipe. This is a matter that requires the greatest care; for
the skin is so very thin and brittle that a little rough handling will
break it to pieces. As a rule it may be easily pushed off the pipe
by a slight pressure behind, or a gentle twisting motion will loosen
its hold; but this latter method can hardly be applied to hairy
larvæ without breaking off the hairs, now rendered very brittle by
the heat.

If you find the slightest difficulty in detaching the skin of a
valuable specimen, it is far better to damage the blowpipe than to
risk spoiling the skin. Supposing your blowpipe is a glass one,
you can easily break off the end of it after making a cut with a very
small triangular file, and the portion thus removed may be left
attached to the skin. Then, after softening the glass blowpipe in a
gas flame or the flame of a spirit lamp, it can be drawn out thin
again for future work. Those who can manipulate glass tubing in
this way will find it far better to lay in a stock of suitable material,
drawing it out when required, than to purchase blowpipes ready
made at the naturalist’s shop.

Very fine hollow stems, such as those of the bamboo cane, may
be used instead of glass; and these possess the advantage of being
easily cut with a sharp knife when there is any difficulty in removing
the skin. Again, whether glass or fine stems are used, a little
grease of any kind placed previously on the end will allow the dried
skin to be slid off with less difficulty.

Preserved larvæ should preferably be mounted on small twigs
or artificial imitations of the leaves of the proper food plants. A
little coaguline applied to the claspers will fix them very firmly on
these twigs or leaves, which are then secured in the cabinet by
means of one or two small pins.[Pg 133]

It is much to be regretted that the natural colours of many
caterpillars cannot be preserved in the blown skins. Some are
rendered much lighter in colour on account of the withdrawal of
the contents, while others turn dark during the drying. In the
smooth-skinned species the natural tints may be restored by painting
or by staining with suitable aniline dyes, but these artificial imitations
of the natural colours are always far less beautiful than the
hues of the living larvæ.

Very few words need be said on the preservation of pupæ.
Many of them do not alter much in form and colour, and therefore
they require no special preparation.

If a pupa has to be killed for the purpose of adding to the value
of the collection, simply plunge it into boiling water, and it is ready
to be fixed in the cabinet as soon as it is quite dry.

The empty pupa cases, too, from which the perfect insects have
emerged, are often worth preserving, especially if the damage done
by the imago on forcing its way out is repaired with the aid of a little
coaguline.

Let all larvæ and pupæ be preserved in their characteristic attitudes
and positions as far as possible, so that each one tells some
interesting feature of the life history of the living being it represents.
Further, enrich your collection by numerous specimens of
the various kinds of cocoons constructed by the larvæ, pinning each
one beside its proper species; and never refuse a place to any
object that relates something of the life history of the creatures
you are studying.


[Pg 134]

CHAPTER XI

THE CABINETARRANGEMENT OF SPECIMENS

The selection of a cabinet or other storehouse for the rapidly
increasing specimens of insect forms is often a matter of no small
difficulty to a youthful entomologist. Indeed, there are very many
points of considerable importance to be considered before any final
decision is made. Freedom from dust, the exclusion of pests, the
convenience of the collector, the depth of his pocket, and the
general appearance of the storehouse must be considered, and it is
impossible, therefore, to describe a form that is equally suitable
to all.

If it is absolutely necessary that the cabinet (or its substitute)
be of a very inexpensive character, and if, at the same time, the
collector has not the mechanical skill necessary for its construction,
then perhaps the best thing he can do is to procure a number of
shallow (about an inch and a half deep) cardboard, glass-topped
boxes, such as are to be obtained at drapers’ shops. For the sake
of uniformity and convenience in packing, have them all of one
size. Glue in small slices of cork just where the insects are to be
pinned, and see that each box is supplied with either camphor or
naphthaline. All the boxes may be packed in a cupboard or in a
case made specially to contain them; and a label on the front of
each will enable you to select any one when required without disturbing
the others.

It may be mentioned here that glass is not necessary, though it
is certainly convenient at times, especially when you are exhibiting
your specimens to admiring non-entomological friends, who have
almost always a most alarming way of bringing the tip of the first
finger dangerously near as they are pointing out their favourite
colours. ‘Isn’t that one a beauty?’ is a common remark, and[Pg 135]
therewith off snaps a wing of one of your choicest insects. When
glass is used, however, see that the specimens are excluded from
light, or the colours will soon lose their natural brilliancy.

Anyone who has a set of carpenter’s tools and the ability to use
them well will be able to construct for himself either a set of store
boxes or a cabinet of many drawers in which to keep his natural
treasures. In this case a few considerations are necessary before
deciding on the form which the storehouse is to take.

A cabinet, if nicely made, forms a very sightly article of furniture;
and, if space can be found for it, is the best and most convenient
receptacle. One of about twelve to twenty drawers will be
quite sufficient for a time; and the few following hints and suggestions
may be useful.

The wood used should be well seasoned, and free from resin.
The drawers should fit well, and slide without the least danger of
shaking. Each one should be lined with sheet cork, about one-eighth
of an inch thick, glued to the bottom, nicely levelled with
sand paper, and then covered with thin, pure white paper, laid on
with thin paste. It is also advisable to cover each with glass,
inclosed in a light wood frame that fits so closely as to prevent the
intrusion of mites.

The drawers may be arranged in a single vertical tier if the
cabinet is to stand on the floor, or in two tiers if it is to be shorter
for placing on the top of another piece of furniture; and glass doors,
fastened by a lock and key, may be made to cover the front if such
are desired as a matter of fancy, or as a precaution against the
meddlesome habits of juvenile fingers.

Store boxes are sometimes chosen in preference to cabinets
because they are more portable, and because they can be arranged
on shelves—an important consideration when floor space is not
available.

These boxes should be cork-lined and glazed like the cabinet
drawers; and if they are made in two equal portions, lined with
cork on both sides, and closing up like a book, they may be arranged
on shelves like books, in which position they will collect but little
dust.

Both store boxes and cabinets are always kept in stock by the
dealers, the former ranging from a few shillings each, and the latter
from fifteen shillings to a guinea per drawer. Knowing this, you
can decide for yourself between the two alternatives—making and
purchasing.[Pg 136]

We have now to consider the manner in which our specimens
should be arranged and labelled.

The table forming Appendix I contains the names of all the
British butterflies and larger moths, and shows their division
into Sections, Tribes, Families, and Genera. This table is the
result of most careful study on the part of leading entomologists,
and shows how, in their opinion, the insects can best be arranged
to show their relation to one another; and you cannot do better
than adopt the same order in your collection.

Complete label lists can be purchased, printed on one side of
the paper only. These, when cut up, supply you with neat labels
for your specimens.

If you intend to study the British Lepidoptera as completely
as possible, you may as well start at once with a sufficiently extensive
cabinet, and arrange all the labels of your list before you introduce
the insects. You will thus have a place provided ready for
each specimen as you acquire it, and the introduction of species[Pg 137]
obtained later on will not compel you to be continually moving and
rearranging the drawers.

Probably the number of blank spaces will at first suggest an
almost hopeless task, but a few years of careful searching and
rearing will give you heart to continue your interesting work.

Arrange all the insects in perpendicular rows. Put the names
of each section, tribe, family, and genus at the head of their
respective divisions, and the names of the species below each insect
or series of insects. The opposite plan, in which the circles
represent the insects themselves, will make this clear.

Three or four specimens of each species are generally sufficient,
except where variations in colouring are to be exhibited. Wherever
differences exist in the form or markings of the sexes, both should
appear; and one specimen of each species should be pinned so as
to exhibit the under side.

Finally, each drawer or box should have a neat label outside
giving the name or names of the divisions of insects that are
represented within. This will enable you to find anything you
may require without the necessity of opening drawer after drawer
or box after box.


[Pg 139]

PART III

BRITISH BUTTERFLIES

We have now treated in detail of the changes through which
butterflies and moths have to pass, and have studied the methods
by which we may obtain and preserve the insects in their different
stages. I shall now give such a brief description of individual
species as will enable the reader to recognise them readily. We
will begin with the butterflies.


CHAPTER XII

THE SWALLOW-TAIL AND THE ‘WHITES’

Family—Papilionidæ

The Swallow-tail (Papilio Machaon)

Our first family (Papilionidæ) contains only one British species—the
beautiful Swallow-tail (Papilio Machaon), distinguished at once
from all other British butterflies by its superior size and the ‘tails’
projecting from the hind margin of the hind wings.

This beautiful insect is figured on Plate I, where its bold black
markings on a yellow ground are so conspicuous as to render a
written description superfluous. Attention may be called, however,
to the yellow scales that dot the dark bands and blotches, making
them look as if they had been powdered; also to the blue clouds
that relieve the black bands of the hind wings, and the round reddish
orange spot at the anal angle of each of the same wings.

It appears that this butterfly was once widely distributed
throughout England, having been recorded as common in various
counties, and has also been taken in Scotland and Ireland; but it
is now almost exclusively confined to the fens of Cambridgeshire,[Pg 140]
Huntingdonshire, and Norfolk. Occasionally we hear of the capture
of single specimens quite outside these localities, sometimes even
in most unlikely spots, where its food plant does not abound. But
we know that Machaon is a general favourite with entomologists,
and that it is sent in the pupal state, by post, to all parts of the
kingdom; so that the occasional capture of the insect far beyond
the borders of its haunts is probably the outcome of an escape from
prison, or of the tender-heartedness of some lover of nature who
could not bear to see such a beautiful creature deprived of its short
but joyous, sunny flight.

You cannot hope to see this splendid butterfly on the wing unless
you visit its haunts during its season—May to August; but the
pupæ may be purchased for a few pence each from most of the
entomological dealers; and if you obtain a few of these and watch
them closely, you may be fortunate enough to see the perfect insect
emerge from its case, and witness the gradual expansion of its
beautiful wings.

The pupa (Plate VIII, fig. 7) itself is a most beautiful object.
Its colour is a pale green, and it is fixed to its support by the tail,
and further secured by a very strong silk band.

The larva (Plate VIII, fig. 1), too, is exceedingly beautiful. Its
ground colour is a lovely green, and twelve velvety black rings
mark the divisions between the segments. Between these are also
black bars, all spotted with bright orange except the one on the
second segment.

A remarkable feature of this larva is the possession of a forked,
Y-shaped ‘horn,’ that is projected from the back, just behind the
head, when the creature is alarmed. If it is gently pressed or
irritated in any way, this horn is thrust out just as if it were an
important weapon of defence. And perhaps it is, for it is the source
of a powerful odour of fennel—one of the food plants of the caterpillar—that
may possibly prove objectionable to some of its numerous
enemies.

The food plants of Machaon are the milk parsley or hog’s
fennel (Peucedanum palustre), cow-parsnip (Heracleum sphondylium),
and the wild angelica (Angelica sylvestris); but in confinement
it will also partake of rue and carrot leaves.

The caterpillar of this species may be found in the fens during
the greater part of the summer. It turns to a chrysalis in the
autumn, and remains in this state throughout the winter, attached
to the stems of reeds in the vicinity of its food plants. The perfect[Pg 141]
insect is first seen in May, and is more or less abundant from this
time to the month of August.

Family—Pieridæ

This family, though known commonly as the ‘Whites,’ contains
four British species that display beautiful tints of bright yellow or
orange.

In many respects the Pieridæ resemble the last species. Thus
the perfect insects have six fully developed legs; the caterpillars
are devoid of bristles or spines; and the chrysalides are attached
by means of silky webs at the ‘tails,’ and strong cords of the same
material round the middle.

All the larvæ are also cylindrical or wormlike in shape; and
their skins are either quite smooth, or are covered with very short
and fine hairs, that sometimes impart a soft, velvety appearance.

The members of this family are remarkable for their partiality
for certain of our cultivated plants and trees; and are, in some
cases, so abundant and so voracious, that they are exceedingly
destructive to certain crops.

The Black-veined White (Aporia Cratægi)

This butterfly may now be regarded as one of our rarities. At
one time it was rather abundant in certain localities in England,
among which may be mentioned the neighbourhoods of Cardiff and
Stroud, also parts of Kent, Sussex, Hampshire, Huntingdonshire, and
the Isle of Thanet; but it is to be feared that this species is nearly
or quite extinct in this country. It is well, however, not to give up
the search for it, and if you happen to be in one of its favoured
localities of former days, you might net all the doubtful ‘Whites’
of large size that arouse your suspicions, liberating them again if,
on inspection, they do not answer to the description of the species
‘wanted.’ This course becomes absolutely necessary, since the
Black-veined White is hardly to be distinguished from the Common
Large White while on the wing.

If you examine a number of British butterflies you will observe
that in nearly all species the wings are bordered by a fringe of hair,
more or less distinct. But the case is different with Cratægi. Here
they are bordered by a black nervure, without any trace of fringe,
thus giving an amount of rigidity to the edges (see Plate I, fig. 2).

The wing rays, or nervures, are very distinct—a feature that[Pg 142]
gave rise to the popular name of the butterfly. In the male they
are quite or nearly black, but those of the fore wings of the female
are decidedly brown in colour. At the terminations of the wing
rays there are triangular patches of dark scales, the bases of which
unite on the outer margins of the wings.

Another peculiar feature of this insect is the scanty distribution
of scales on the wings. This is particularly so in the case of the
female, whose wings are semi-transparent in consequence.

The butterfly is on the wing during June and July, at which
time its eggs are laid on the hawthorn (Cratægus Oxyacantha)
or on fruit trees—apple, pear and plum.

A vigorous search of these trees in the proper localities may
reveal to you a nest of the gregarious larvæ, all resting under the
cover of a common web of silk. These remain thus under their
silken tent throughout the hottest hours of the day, and venture out
to feed only during the early morning and in the evening.

When the leaves begin to fall in the autumn, they construct a
more substantial web to protect themselves from the dangers of the
winter, and in this they hybernate till the buds burst in the
following spring. They now venture out, at first during the mildest
days only, and feed voraciously on the young leaves, returning to
their homes to rest. Soon, however, they gradually lose their
social tendencies, till at last, when about half or three-quarters
fed, they become quite solitary in their habits.

In May they are fully grown, and change to the chrysalis state
on the twigs of their food trees.

The larva is black above, with two reddish stripes. The sides
and under surface are grey, the former being relieved by black
spiracles.

The pupa (page 45) is greenish or yellowish white, striped with
bright yellow, and spotted with black.

It is probable that the reader will never meet with this insect in
any of its stages. But, though it may have left us, it is still very
abundant on the Continent, where it does great damage to fruit
trees; and the foreign pupæ may be purchased of English
dealers.

The Large White (Pieris Brassicæ)

We pass now from one of the rarest to one of the most abundant
of British butterflies. Everybody has seen the ‘Large White,’
though we doubt whether everybody knows that this insect is not[Pg 143]
of the same species as the two other very common ‘Whites.’ The
three—Large, Small, and Green-veined—are so much alike in
general colour and markings, and so similar in their habits and in
the selection of their food plants, that the non-entomological, not
knowing that insects do not grow in their perfect state, may
perhaps regard the larger and the smaller as older and younger
members of the same species. But no—they are three distinct
species, exhibiting to a careful observer many important marks by
which each may be known from the other two.

On Plate I (fig. 3) will be seen a picture of the female Brassicæ,
in which the following markings are depicted: On each fore wing—a
blotch at the tip, a round spot near the centre, another round
one nearer the inner margin, and a tapering spot on the inner margin
with its point toward the base of the wing. On the hind wings
there is only one spot, situated near the middle of the costal
margin.

The male may be readily distinguished by the absence of the
black markings on the fore wings, with the exception of those
at the tips. He is also a trifle smaller than his mate.

This butterfly is double-brooded. The first brood appears in
April and May, the second in July and August; and the former—the
spring brood—which emerges from the chrysalides that have
hybernated during the winter, have grey rather than black tips to
the front wings.

The ova of Brassicæ may be found on the leaves of cabbages in
every kitchen garden, also on the nasturtium, during May and
July. They are pretty objects (see fig. 10), something like little
bottles or sculptured vases standing on end, and are arranged
either singly or in little groups.

As soon as the young larvæ are out—from ten to fifteen days
after the eggs are deposited—having devoured their shells, they
start feeding on the selfsame spot, and afterwards wander about,
dealing out destruction as they go, till little remains of their
food plant save the mere stumps and skeletons of the leaves.

The ground colour of the caterpillar is bluish green. It has a
narrow yellow stripe down the middle of the back, and two similar
but wider stripes along the sides; and the surface of the body is
rendered somewhat rough by a number of small black warty projections,
from each of which arises a short hair.

When fully grown, it creeps to some neighbouring wall or
fence, up which it climbs till it reaches a sheltering ledge. Here[Pg 144]
it constructs its web and silken cord as already described (page 36),
and then changes to a bluish-white chrysalis, dotted with black.
The butterflies of the summer brood emerge shortly after, but
the chrysalides of the next brood hybernate till the following
spring.

It is remarkable that we are so plagued with ‘Whites’ seeing
that they have so many enemies. Many of the insect-feeding birds
commit fearful havoc among their larvæ, and often chase the
perfect insects on the wing, but perhaps their greatest enemy is the
ichneumon fly.

Look under the ledges of a wall of any kitchen garden, and you
will see little clusters of oval bodies of a bright yellow colour.
Most gardeners know that these are in some way or other
connected with the caterpillars that do so much damage to their
vegetables. They are often considered to be eggs laid by the
larvæ, and are consequently killed out of pure revenge, or
with a desire to save the crops from the future marauders.

No greater mistake could be made. These yellow bodies are
the silken cocoons of the caterpillar’s own foes. They contain the
pupæ of the little flies whose larvæ have lived within the body of
an unfortunate grub, and, having flourished to perfection at the
expense of their host, left its almost empty and nearly lifeless
carcase to die and drop to the ground just at the time when it
ought to be working out its final changes. Often you may see the
dying grub beside the cluster of cocoons just constructed by its
deadly enemies. Should you wish to test the extent of the
destructive work of these busy flies, go into your garden and collect
a number of larvæ, and endeavour to rear them under cover. The
probability is that only a small proportion will ever reach the
final state, the others having been fatally ‘stung’ before you took
them.

The Small White (P. Rapæ)

This butterfly closely resembles the last species except in point
of size. The male, represented on Plate I (fig. 4), has a dark grey
blotch at the tip of each fore wing, a round spot of the same colour
beyond the centre of that wing, and another on the costal margin
of the hind wing. The female may be distinguished by an
additional spot near the anal angle of the fore wing.

Although this and the two other common butterflies (Brassicæ
and Napi) that frequent our kitchen gardens are usually spoken of[Pg 145]
as ‘Whites,’ a glance at a few specimens will show that they are
not really white at all, but exhibit delicate shades of cream and
yellow, inclining sometimes to buff. The under surfaces are particularly
noticeable in this respect, for here the hind wings and the
tips of the fore wings display a very rich yellow.

The species we are now considering is also very variable both in
its ground colour and the markings of the wings. The former is in
some cases a really brilliant yellow; and the latter are in some
cases entirely wanting.

Rapæ is double-brooded, the first brood appearing in April and
May, and the other in July and August.

During these months the eggs may be seen in plenty on its
numerous food plants, which include the cabbages and horse-radish
of our gardens, also water-cress (Nasturtium officinale), rape
(Brassica Napus), wild mustard (B. Sinapis), wild mignonette
(Reseda lutea), and nasturtium (Tropæolum majus).

The eggs are conical in form—something like a sugar loaf, with
ridges running from apex to base, and very delicate lines from
ridge to ridge transversely.

The young larvæ often make their first meal of the shell, and
then attack the food plant so voraciously that they are fully grown
in about three or four weeks. In colour they are of a beautiful
glaucous green, hardly distinguishable at times from the leaves on
which they rest. A yellow stripe runs along the middle of the
back, and lines of yellow spots adorn the sides; and the whole body
is covered with very short hairs, each one arising from a minute
warty projection.

The pupæ may be found during the same seasons and in the
same situations as those of Brassicæ. They are very variable in
colour. Some are of a very pale grey or putty colour, some are
decidedly brown, and others of a greenish tinge; and they are
often spotted and striped with dark grey or black.

The Green-veined White (P. Napi)

A non-observant beginner at entomological work may easily
mistake this insect for the last species, for the ground colour and
markings are very similar, even to the features by which the sexes
are distinguished from each other; but an inspection of the under
surface will give a ready means of identification, for here the wing
rays are bordered with black scales which, by contrast with the[Pg 146]
rich yellow around them, often appear of a greenish hue. The
butterfly receives its popular name from this circumstance.

A careful observer, however, will readily find distinguishing
marks on the upper side, for here also the chief ‘veins’ are more
or less accompanied with black scales, especially the extremities of
those of the fore wings, where little triangular blotches are often
distinctly formed; and the dark veining of the under surface of the
hind wings frequently shows through. The under side of this
insect is shown on Plate I (fig. 5).

This butterfly is not so abundant as the two preceding, but is
widely distributed throughout England, and is in most parts
decidedly plentiful.

The first brood (for it also is double-brooded) appears during
April and May, and the second in July and August.

The eggs are very similar to those of Rapæ, resembling ribbed
and striated sugar loaves; and the larvæ are of the same rich glaucous
green, but may be identified by the black spiracles surrounded by
yellow rings. In our gardens we may find both eggs and larvæ on
mignonette and horse-radish; the other food plants of this species
include the water-cress (Nasturtium officinale), winter cress
(Barbarea vulgaris), rape (Brassica Napus), cuckoo-flower
(Cardamine pratensis), and Jack-by-the-hedge (Sisymbrium
Alliaria
).

The pupa is greenish, and marked with small black dots.

The Bath or Green-chequered White (P. Daplidice)

There is no doubt that many butterflies migrate from one country
to another across the seas; and as the Bath White is very
common on the other side of the Channel, and has been taken very
sparingly in England almost exclusively in the south-east, it is
highly probable that the majority of those that have been captured
here are specimens that have taken a voluntary trip across the
water, or have been blown over during rough weather.

This butterfly is one of our greatest rarities, and the capture of a
specimen in England is an event that must necessarily be recorded
in our entomological literature. It seems that Daplidice has bred
in England, for its caterpillars have been found at large on one or
two occasions, so I will give a short description of the various
stages of the insect, with a hope that some of my readers may be
fortunate enough to meet with it.[Pg 147]

The female butterfly is shown on Plate I, fig. 6. From this it
will be observed that each of the fore wings is tipped with a rather
large smoky-black blotch, in which are four white spots. A double
spot of the same colour also occupies a place near the centre of the
wing, and another smaller and round one lies near the anal angle.
The hind wings are clouded with grey, and bordered along the
hind margin with distinct smoky-black spots.

The male may be distinguished from the female by the absence
of the spot near the anal angle of the fore wings, and of all the
clouds and spots of the hind wings. Nevertheless the latter have
a decidedly clouded appearance, but this is due to the markings of
the under surface showing through them.


Fig. 65.—The Bath White—Under
Side.

The under side of both sexes is most beautifully marked—the
fore wings resembling the upper sides, but the hind pair chequered
with a beautiful soft green on a
pale yellow ground.

The eggs of this insect are
deposited during April and May,
and again in August or September—for
it is, like the other
‘Whites,’ double-brooded—on
two species of Wild Mignonette
(Reseda lutea and R. luteola).

The caterpillars, which are
of a bluish colour, with two
yellow stripes down the back, and
two others along the sides, may be looked for in June and September.
Those of the first brood only have been taken in this
country, while the others on the Continent change to the chrysalis
in the autumn, and hybernate in this state throughout the winter.

The chrysalis is of a brownish colour, and closely resembles that
of the Small White in form.

Those in search of this rare British insect should wander along
the south-east coast, and net all the doubtful slow-flying small
Whites (Daplidice is rather slow and heavy on the wing), and
their perseverance may be rewarded with a prize that will ever be
a reminder of a glorious catch and an eventful day. If you fail in
this, and most probably you will, rather than remain a stranger to
this beautiful and interesting insect, fill up the blank in your
cabinet with a foreign specimen, which can be obtained at any time
for a few pence, but be careful to label it ‘not British,’ in order[Pg 148]
that your brother collectors may not be deceived, or be led to make
any unnecessary inquiries.

The Orange Tip (Euchloë Cardamines)

No one could possibly mistake the male of this species for any
other British butterfly, the popular name alone giving quite
sufficient information for its identification, but the female Orange
Tip is not tipped with orange, and its markings, both above and
beneath, resemble those of Daplidice so nearly that the same
written description might apply almost equally well to both.

On Plate I (fig. 7) is shown the upper side of the male, and
just opposite it (fig. 8) the under surface of the same. The female
is usually a little larger than her mate, and is marked similarly on
both sides except that the bright orange blotch is entirely wanting.
She may always be distinguished from Daplidice by the smaller
size of the white spots that break the dark blotch at the tip of the
fore wing; also by the very small size of the dark spot in the
centre of the same wing. The green chequerings of the under side
of the hind wings are also more sharply defined, and the insect is
generally of a lighter build.

Like many other butterflies, the Orange Tip is subject to variations
in colouring. Sometimes a pale but bright yellow takes the
place of the white ground, and the orange blotch of the male is
occasionally present on the upper or lower surface only.

Cardamines is a single-brooded insect, and is essentially a
creature of the spring, at which time it may be found in abundance
in lanes, meadows, and clearings in woods throughout the British
Isles. Its flight is so light and airy that even the female may
easily be distinguished from other Whites when on the wing, while
the brilliant orange of the male, intensified by the bright rays of
the spring sun, may be identified at some considerable distance.

The food plants of Cardamines include the cuckoo-flower
(Cardamine pratensis) and the bitter cress (C. impatiens), after
which the insect is named, also water-cress (Nasturtium officinale),
winter cress (Barbarea vulgaris), rock cress (Arabis perfoliata),
hedge mustard (Sisymbrium officinale), Jack-by-the-hedge (S.
Alliaria
), wild mustard (Brassica Sinapis), &c., and the eggs of
the butterfly may be found on these during May and June.

The caterpillar (Plate VIII, fig. 2) is green, with a white stripe
on each side, and its body is covered with short hair. In July it is[Pg 149]
fully grown, and ascends a stem of the food plant to prepare itself
for its long winter sleep.

The chrysalis (Plate VIII, fig. 8) is a very peculiar object. Both
ends are much elongated and sharply pointed; and the foremost
extremity stands out at an angle with the stem to which it is
attached.

This butterfly should be looked for during April and May, but in
mild seasons it may often be met with in March.

The Wood White (Leucophasia Sinapis)

The distinguishing feature of this butterfly (see Plate II, fig. 1)
is the extreme lightness and delicacy of its build. Its wings are
narrow, and rounded at the tips; and the only mark to relieve the
white ground of the upper side is a squarish blotch at the tip of the
fore wing, and even this is either very indistinct or entirely absent
in the female. The under surface is clouded with a pale greenish
tint.

This insect may be looked for in May and again in August, in
paths and clearings in woods, where it moves along with a slow but
steady flight, hardly ever seeming to rest for a moment. It is not
by any means a common butterfly, but is very widely distributed,
and sometimes appears in considerable numbers in certain favoured
spots. Among the localities recorded may be mentioned Torquay,
Exeter, Plymouth, South Dorset, New Forest, Reading, Darent
Woods, Morecambe Bay, Haslemere, Windermere, &c.

The caterpillar is of a beautiful green colour, and is covered with
short whitish hairs. A darker green stripe runs down the middle
of the back, and a bright yellow stripe along each side. Its food
plants are the tufted vetch (Vicia Cracca), bird’s-foot trefoil (Lotus
corniculatus
and L. pilosus), bitter vetch (Lathyrus tuberosus),
and the everlasting pea (L. sylvestris).

The chrysalis is a very beautiful object. Its colour is a delicate
green, tinged with pink; and the wing-cases project in beautiful
curves much beyond the general surface.

The Pale Clouded Yellow (Colias Hyale)

The ground colour of this butterfly (Plate II, fig. 2) is very variable.
It is usually a sulphury yellow, and on this account the insect
is commonly known as the Clouded Brimstone; but sometimes the
yellow is exceedingly pale—almost white—and tinged with green.[Pg 150]

A very large black blotch, broken by indefinite patches of the
ground colour, fills up the tip of each fore wing, and extends to the
anal angle, becoming narrower as it approaches this point. A black
oval spot lies just above the middle of this wing.

The hind wings are bordered with black, and a conspicuous spot
of deep yellow lies very near the centre of each.

The antennæ are rather short, compared with those of the preceding
members of this family, and are distinguished by their
reddish-brown colour.

The male and female of this species are similarly marked, but
the ground colour of the latter is commonly paler.

This is not by any means a very common butterfly with us,
though it is very plentiful on the other side of the Channel; but it
has a way of taking us by surprise in certain seasons, and then
almost neglecting us for several years together.

Its head quarters are certainly the coasts of Kent and Sussex,
but it has been taken in considerable numbers as far west as Cornwall,
and also to a less extent in some of the midland and northern
counties. It is particularly fond of lucerne and clover fields,
especially those that are situated close to the sea cliffs; and often
it may be seen flying over the beach, sometimes even flitting over
the breakers away from land till at last it disappears in the distance.
This maritime tendency of Hyale makes it probable that a
large number of those that are seen on our south-east coasts have
made a passage across the narrow end of the Channel.

The eggs are laid in spring, by females that have hybernated
throughout the winter, on various leguminous plants, including the
lucerne (Medicago sativa), black medick (M. lupulina), purple and
Dutch clovers (Trifolium pratense and T. repens), and the bird’s-foot
trefoil (Lotus corniculatus), and on these plants you may search
for the larva, though it can scarcely be said that you are likely to
find it.

The caterpillar is green, with black dots, and a yellowish stripe
on each side. When fully grown it ascends a stem of its food plant
and changes to a green chrysalis with yellow stripes.

Hyale is single-brooded in England, although two broods
regularly appear on the Continent. In our country the perfect insects
emerge during July and August. Many of these die before
the approach of winter; but, as we have already observed, some
hybernate and deposit their eggs in the following spring.[Pg 151]

The Clouded Yellow (Colias Edusa)

Not only are this and the last species similarly named, but a
glance at the figures will show that they much resemble each other
in appearance; and we shall also learn presently that in their habits
and life history they have much in common.

The male Edusa is shown on Plate II (fig. 3), and when we
compare it with its relative on the opposite side, we are at once struck
with the superior richness of the brilliant orange or saffron of the
ground colour. The black border of both fore and hind wings is also
denser, wider, and more extensive. The whole of the yellow area
of the hind wings is dusted more or less with black scales, with the
exception of a round central spot of deep orange, corresponding with
the orange spots on the hind wings of Hyale.


Fig. 66.—The Clouded Yellow—Female.

The female, which is shown in the accompanying woodcut, is
generally larger than the male, and is further distinguished by the
very pale yellow spots
that break the black
border of both pairs of
wings.

Edusa further resembles
Hyale in the reddish
colour of the antennæ;
and, in both the species,
the red legs form a
pleasing contrast with the
yellow furry surface of the
under side of the thorax.

There is a variety of the female of this butterfly, in which the
ground colour is a very pale yellow, almost white. The hind wings
are more thickly dusted with black scales than in the normal insect,
and the orange spots of these wings show up much more conspicuously
from the contrast with their surroundings.

It is usual to apply distinct names to constant varieties of species—names
that are to be added to the ordinary title. In this particular
case the distinguishing name is Helice, so that we should speak
of the variety of Edusa above mentioned as:

Colias Edusa, var. Helice

Like Hyale, Edusa is particularly capricious in its appearance.
In certain summers it absolutely swarms in favourite localities,[Pg 152]
while during the intervals between such remarkable appearances—usually
several years—it is positively scarce. The last favoured
season was the summer of ’92, during which (from the beginning of
August to the end of the summer) dozens might easily have been
caught in an hour or two; in fact, so plentiful were they in many
places, that they were continuously in sight, often several at one time.

Those in search of this insect should repair to the south coast,
especially the south-east, and where lucerne and clover fields are
in flower. It has very decided maritime tendencies, and may often
be seen flying over the cliffs and beaches, and even skipping over the
breakers; but, at the same time, it is more or less plentiful in many
inland districts. It has been taken in many parts of Ireland and
Scotland, particularly along the southern coasts of these countries;
but its head quarters are undoubtedly the southern cliffs of England,
from Cornwall to Kent, and also the hilly inland districts of the
south-eastern counties.

Edusa catching is very lively sport, and is likely to prove
sufficient for any lover of outdoor exercise under a scorching sun;
for this butterfly is not only very powerful on the wing, but its
flights are usually long, so that a good run is often absolutely
necessary in order to capture it. On very hilly ground, such as
Edusa loves, chase is often hopeless, and then it is necessary to
resort to stratagem. In such a case the best plan is to make a
very cautious approach when the insect has been observed to settle,
and then secure it with a sudden down-stroke of the net.

The eggs are laid during May and June by a few females that
have survived the winter.

The caterpillar may be found in June and July on its food
plants, the chief of which are the bird’s-foot trefoil (Lotus corniculatus),
and the purple and Dutch clovers (Trifolium pratense and
T. repens). Its colour is grass-green, and it is marked with a narrow
whitish stripe on each side, which is broken by the yellow of the
spiracles.

The chrysalis is of a pale yellowish green, and is marked with
yellow stripes and reddish-brown dots.

The Brimstone (Gonopteryx Rhamni)

This, the last member of the present family, is remarkable for
the graceful outline of its wings. The costal margins of the fore
pair are most beautifully arched, and both pairs are sharply angled
on the hind margins. This latter characteristic is quite unique[Pg 153]
among British butterflies, though we shall presently meet with
instances of angular projections on hind wings only.

The ground colour of the male (Plate II, fig. 4) is a rich sulphury
yellow, with a greenish tinge. That of the female is a very
pale greenish yellow. The only conspicuous markings are small
saffron spots, one near the centre of each wing. The antennæ are
red, short, and beautifully curved; but, unlike the two preceding
species, the legs are almost white.

The eggs of this butterfly are laid in April on the two species of
buckthorn (Rhamnus catharticus and R. Frangula) by the females
that have successfully weathered the winter. They are of a bright
yellow colour, and are usually hatched in about a fortnight.

The body of the caterpillar is green, and it is thickly covered
with little black wart-like projections. A pale stripe also runs
along each side. During May and June it may be found on its
food plants, and toward the end of the latter month it attaches itself
by a silken carpet and belt to the under side of one of the leaves.

The chrysalis is of a very peculiar shape, the body being curved,
and the wing cases standing out prominently beyond the general
surface. Its colour is a bright apple green marked with yellow,
and it is so transparent that certain of the structures can be seen
through its skin.

The perfect insect emerges in about three weeks after the change
to the chrysalis; and may be looked for from July to the end of the
summer. This period may be regarded as the best time in which
to hunt for Rhamni, but it is to be noted that this butterfly makes
its appearance during all months of the year, even though it is single-brooded.

A large number seem to hybernate, and their winter sleep is so
light that the welcome rays of the sun on a mild day, even during
the bleak months of November to February, will often call them out
from their hiding places. Then, as a rule, the hybernating butterflies
do not live long after depositing their eggs for the future
brood; but the Brimstone often lives on till its offspring have themselves
attained the perfect state, so that it is possible to capture the
insects of two different years both on the same day. In such a case
it is generally easy to distinguish between the two, for the newly
emerged specimens are beautifully bright and fresh in colour,
while those of the previous year are more or less faded and worn,
their wings being often semi-transparent through the loss of scales,
and frequently disfigured by the stains of mildew.


[Pg 154]

CHAPTER XIII

THE FRITILLARIES, VANESSAS, AND THE PURPLE
EMPEROR

Family—Nymphalidæ

We now come to a rather large family, which contains some of our
largest and most brilliant butterflies. Some of them display the
most gaudy colours, and others exhibit patches of a beautiful metallic
lustre.

If you were to see all the members of this family side by side,
they might strike you as being so varied in their appearance that
you would wonder why they are all placed in one family group.
But, were you to see, in addition to the perfect insects, all their
larvæ and chrysalides, the reason would be made clear at once, for
these earlier stages are seen to resemble each other in certain points
at the very first glance. The former are all provided with peculiar
spines, and the latter are all more or less angular, and are all suspended
to a silken carpet by means of hooks at the tip of the abdomen,
and have no belt as we have observed in the case of the
Pieridæ.

The perfect insects, too, although so varied in colouring, are
alike in that they have only four walking legs, the first pair being
so imperfectly developed as to be useless for this purpose.

This family includes the Fritillaries and the Vanessas.

The Small Pearl-bordered Fritillary (Argynnis Selene)

The interesting group of butterflies known as the Fritillaries
vary considerably in size, but are remarkably uniform in the
ground colour of the wings, which, in all cases, is a rich golden or
sienna brown; and this ground is chequered with darker colours in
such a manner as to remind one of the petals of the wild flower[Pg 155]
known as the Snake’s Head or Fritillary—hence the popular name
of the group.

The Small Pearl-bordered, our first example, is one of the lesser
Fritillaries, and is shown in Plate II (fig. 5).



Fig. 67.—The Small Pearl-bordered
Fritillary—Under
Side.

The arrangement of the black markings on the upper surface
will be readily made out from the coloured plate, but the pattern
of the under side will require a little special notice, for it is here,
as with the other Fritillaries, that we find the chief marks by
which we identify the species. On this side (fig. 67) the fore wings
are light orange brown, with a patch of darker brown near the tips,
and spotted with a dull black. The hind wings have the light
brown displaced by a very warm chestnut tint, some yellow, and
bright silvery spots.

Seven silvery spots of triangular form border the hind margin.
A large one occupies the centre
of the wing, and ten others are
somewhat irregularly scattered
over other parts of the wing—five
between the central spot and
the hind margin, and five between
it and the costa.

All the spots on these wings,
whether yellow, chestnut, or silver,
are bordered by a narrow black
line.

Selene is not a very abundant butterfly, but is widely distributed
in England, and is also found in parts of Scotland. Its favourite
resorts are clearings in woods, especially those of Kent and other
southern counties.

It appears in May and June, in which latter month it deposits
its eggs on the dog violet (Viola canina).

The caterpillar is not fully grown at the end of the summer,
and hybernates during the winter among the roots of its food
plant. In the following spring it emerges again, and feeds till
May, when it changes to the chrysalis on a stem. It is less than
an inch long when fully grown, and is of a dark-brown colour.
Six rows of hairy spines are arranged longitudinally on its
body.

The chrysalis is greyish brown, and has a number of very short
projections corresponding with the spines of the caterpillar.[Pg 156]

The Pearl-bordered Fritillary (Argynnis Euphrosyne)

There is very little difference in the size of this and that of the
last species, but Euphrosyne (Plate II, fig. 6) is generally a trifle
larger. The two butterflies are also very similar in appearance;
indeed, they are so much alike on the upper side that it is impossible
to decide on the name of either without an examination of the
under surface.


Fig. 68.—The Pearl-bordered
Fritillary—Under Side.

Euphrosyne has a border of seven triangular silver spots on
each hind wing, exactly corresponding with those of Selene. It
has also the large central spot of silver. But, beside these, there is
only one other, and that is situated in the basal angle. Thus there
are only nine silvery or pearly
spots on each hind wing of
Euphrosyne, while there are
seventeen on Selene. This
will form a ready means of
distinguishing between the two
species.

The seasons and localities
of this butterfly correspond
very closely with those of the
last species, but it is much more common, and may be found in
abundance in nearly all our southern woods during May and
June.

The caterpillar, also, feeds on the same plant (dog violet) as
Selene. It is black, with whitish lines along the sides; and is
provided with a number of bristly spines.

The chrysalis is of a grey-brown colour, with small dots of a
paler tint on the wing cases; and its body has a number of short
conical projections exactly corresponding with the spines of the
caterpillar.

The Queen of Spain Fritillary (Argynnis Latona)

We now pass from the commonest to the rarest and most
prized of our wood butterflies—The Queen of Spain (Plate II,
fig. 7). This royal personage is not easily mistaken for any of the
meaner Fritillaries even when the upper surface only is examined,
as the concave hind margins of the fore wings serve as an almost
conclusive mark of distinction. The rich tawny brown of this side[Pg 157]
is boldly marked with black, and the long hairs and scales of the
bases of the wings are tinged with green.


Fig. 69.—The Queen of Spain
Fritillary—Under Side.

The under side presents a most beautiful appearance. Here the
ground colour is paler than that of the upper side. The fore wings
are spotted with black, and have a few small patches of silver at the
tips. Each hind wing has no fewer than twenty-four bright silvery
spots. Seven of these, mostly of large size, adorn the hind margin,
and above each of these is a small one in the middle of a little patch
of dark brown. The arrangement of the others is not quite so
easily described, but may be readily made out from our illustration.

This rare gem among British butterflies has been taken in
many localities, but in very small numbers. Seeing that it is a
common insect on the other side of the Channel, and that the
British captures have been made chiefly in the Isle of Wight and
on the south coast, I am
inclined to believe that
many of the highly valued
genuine Britishers have no
right to their title, but are
visitors that have spent
only a few days within our
shores, having flown or been
blown across the sea.

It is not likely that
many of my readers will
ever meet with Latona
during their rambles in our
own country, and if they are anxious to have the species represented
in their collections, they will probably have to purchase either a
British or a foreign specimen, the former of which will command
a very high price, while the latter may be obtained for three or four
pence.

The perfect insect may be looked for in August and September,
during which time the eggs are laid on the leaves of violets and the
heartsease (Viola canina, V. odorata, and V. tricolor).

The caterpillar is brown, with numerous yellowish spines, and
has three whitish or yellowish stripes—one down the middle of the
back and one along each side. It hybernates during the winter,
and is fully grown in the following June or July. I hope that my
reader will be so fortunate as to secure either this or some other
stage of this rare and beautiful insect. The chances are decidedly[Pg 158]
against him, but that is no reason why he should abstain from a
vigorous search when he happens to be ‘doing’ the southern
counties.

The Dark-green Fritillary (Argynnis Aglaia)

This butterfly is larger than Latona, as will be seen by reference
to Plate II, fig. 8. Its colour is, as usual with the Fritillaries, a
tawny brown with black markings. The female is usually larger
than the male, and she is further distinguished by the ground
colour being darker and the black markings larger.


Fig. 70.—The Dark-green Fritillary—Under
Side.

The under side of the fore wings is very similar in colour and
markings to the upper, but there are silvery spots near the tips.
The hind wings are beautifully
tinted with olive
green and brown, and
studded with silver. The
arrangement of the latter
is not easily described, but
is accurately represented
in the accompanying
woodcut.

The favourite resorts
of this insect are wooded
spots, and also heaths and
downs clad with heather
or ferns, where its food
plant (the dog violet) lies scattered; but it seems to be less partial
to woods than the other Fritillaries. It is very widely distributed
throughout England, and is common in parts of Scotland and
Ireland.

The perfect insect is on the wing in July and early August.

The caterpillar first appears toward the end of August, and
commences its period of hybernation among the roots of its food
plant before it has grown to any considerable size. It comes out
again in the spring, and continues to feed till the beginning or
middle of July, and then changes to the chrysalis state, after protecting
itself by binding three or four leaves together.

Its colour is a velvety black, with dark and glossy grey between
the segments. There is a double yellow line along the back, and a
thin line of orange yellow on each side below the spiracles. It has
a number of black hairy spines, arranged in six longitudinal rows.[Pg 159]

The chrysalis is of a shiny black colour, with brownish abdomen;
and the conical projections are black with yellow tips.

The High-brown Fritillary (Argynnis Adippe)

The upper side of this butterfly is so much like that of Aglaia
that it would be difficult indeed to give a written description of
one that did not almost equally well apply to the other; so we look
to the under surface for the chief marks by which we can distinguish
between them.


Fig. 71.—The High-brown Fritillary.

On this side (Plate III, fig. 1) the fore wings are much the same
as those of Aglaia. The hind wings, too, are very similarly coloured
and marked, but here we have a distinguishing feature in a row of
rust-red spots with silvery
centres, just inside
the silver border of the
hind margin.

This butterfly is common
in open spaces of
woods in many parts of
England, more particularly
in the south, and
seems to be also fond of
hilly heaths and moors.

It is on the wing in
July, and, towards the end of this month and in the beginning of
August, the eggs are laid on the leaves of the dog violet (Viola
canina
) and heartsease (V. tricolor).

The young caterpillar emerges about two weeks later, and feeds
only for a short time before it seeks out its winter quarters among
the dead leaves at the root of its food plant. The feeding is resumed
in the spring, and continued till the month of June, when it is fully
grown. At this time it is about an inch and a half long. Its head
is black, and its body pinkish brown. A white line extends down
the back, but is interrupted by several black marks. The spines,
of which there are six rows, are white, with pinkish tips.

The Silver-washed Fritillary (Argynnis Paphia)

This beautiful and noble butterfly is the largest of the Fritillaries,
and the most powerful on the wing. During the latter part of June[Pg 160]
and throughout July it may be seen gracefully sweeping through
the trees and undergrowth of woods, often settling down on a
favourite flower for a short time. So strong is its flight that it is
useless to attempt to pursue it for any distance. Sometimes it will
sail along a wooded path, followed at short intervals by others of
its species, and may be taken in the net as it passes. But perhaps
the most successful method of netting Paphia is to wait till it
has settled, and then secure it by a quick upward or side stroke
of the net. If then you miss your aim, off it will dart, sailing
over the tree tops till, in a very short time, it is quite out of
sight.


Fig. 72.—The Silver-washed Fritillary—Under Side.

The upper side of this butterfly is shown in Plate III, fig. 2,
where the general arrangement of the black spots on the rich
orange-brown ground is carefully marked. There is a considerable
difference between the male and female of this species. The figure
on Plate III represents the male. The female does not possess
the broad black lines that follow the course of the veins of the fore
wings; the basal portions of all four wings are also tinged with a
rich olive-brown colour, often with a decided tendency to green;
and the black spots of all the wings are larger.

The under side is particularly rich in its decorations. The front
wings are of the usual orange brown, chequered with black. The
hind wings are partly brown and partly orange, and exhibit beautiful
greenish reflections. They have also two bars of silver, and a silvery
spot in the basal angle, all with rather indefinite outlines.[Pg 161]

The female lays her eggs late in July on the food plants (Viola
canina
and V. odorata) or on the moss that surrounds them.

About two weeks later the young caterpillar is out and feeding;
and then, after a few more weeks, while it is yet very small, it hides
among the dead leaves at the roots. Early in the spring it resumes
its feeding, and is full grown at the end of May.

The colour of the caterpillar (Plate VIII, fig. 3) is black, and
there are two yellow lines along the back, separated by a black stripe,
also one yellowish line on each side. Its body is adorned with
reddish-brown spines, two of which, situated just behind the head,
are longer than the others.

The chrysalis (Plate VIII, fig. 9) is greyish, marked with
metallic spots, and has a number of angular projections representing
the spines of the larva.

Paphia is to be met with in woods in all parts of England and
Wales. It has also been observed in Ireland, but is rarely seen
in Scotland.

The Greasy Fritillary (Melitæa Aurinia)

Unlike the other Fritillaries, this species (Plate III, fig. 3)
exhibits a variety of shades on the upper surface. A broad band of
sienna brown stretches across each wing, near to and parallel with
the hind margin. The other parts of the wings are marked with
patches of sienna, orange, and yellow, separated by black lines and
bands. The margins are all black, and inside the broader margin
of the hind wing is a row of six very
pale yellow spots. The broad sienna
band of the hind wing is also
divided by narrow black lines into
seven parts, six of which have black
centres.


Fig. 73.—The Greasy Fritillary—Under
Side.

The under surface of the fore
wings has indefinite yellowish and
tawny patches, which look as if they
had been greased and smeared. The hind wings are marked with
pale yellow and deep orange; a broad band of the latter, near the
hind margin, is divided into segments, each of which has a yellow
spot with black in the centre.

This is a very local insect, although it is widely distributed
throughout England and Wales. It also occurs sparingly in Scotland
and Ireland. Its food plants are the honeysuckle (Lonicera[Pg 162]
Periclymenum), devil’s-bit scabious (Scabiosa succisa), and the
plantain (Plantago); and its chief resorts are damp meadows
and marshy places, where these plants (more especially the
scabious) abound.

The butterfly appears about the end of April or in June.

The caterpillars emerge from the eggs towards the end of the
latter month, and always feed in groups under the cover of a silken
web. Like the preceding species they hybernate during the winter,
and commence feeding again in the spring. They are fully grown
about the end of April.

In colour the caterpillar is velvety black, dotted with white, and
its body is covered with short bristly spines. When fully fed it
seeks the shelter of a curled leaf or dense herbage, suspends itself
by the hind claspers to a silken carpet, and then changes to a creamy
white chrysalis with black dots.

The Glanville Fritillary (Melitæa Cinxia)

The pattern of the upper side of this Fritillary (Plate III,
fig. 4) is very similar to that of Aurinia, but the ground colour
is a uniform tawny brown, and the fringes of the wings are of a
very pale straw colour, barred with black.


Fig. 74.—The Glanville
Fritillary—Under Side.

The under side of the fore wings is tawny brown, with straw-coloured
tips bearing black markings. The hind wings have four
alternate bands of brown and straw
colour, and a patch of straw colour at
the base. The marginal yellow band has
six or seven black spots. The brown
band next to it is divided into six segments
with black borders, each with a
black spot. The next yellow band has
also a row of black spots. The inner
fulvous band is very irregular; and inside
this is the yellow base with six spots.

This is another local insect—very local indeed, for it seems to
have been found only in a few spots outside its head quarters, the
Isle of Wight. Those in search of it should carefully scan the
rough cliffy parts of the island, wherever the species of plantain
(Plantago Coronopus and P. maritima) are plentiful, these being
the food plants of the larvæ. It first appears on the wing in May,
but may be found till the end of June.[Pg 163]

The caterpillars, which are black and spiny, with reddish head and
legs, begin to feed in August, and as soon as the chilly weather sets
in they hybernate in groups under the cover of a tent constructed
by binding together leaves or blades of grass. In the spring they
start out again, and feed till the end of April, at which time they
change to dark brownish and smooth chrysalides.

The Heath Fritillary (Melitæa Athalia)

Both the upper and under sides of this butterfly are shown on
Plate III (figs. 5 and 6), and it will be observed from these that its
general appearance is very similar to that of Cinxia.

The upper surface is of the same tawny brown, barred and striped
with black, and the fringes of the wings are pale yellow, interrupted
by small patches of black.

The under surface of the fore wings has the same ground colour
with the exception of the tips, which are yellow; and the whole is
marked with black, as in the illustration. The hind wings are pale
yellow, with two broad bands of brown corresponding with those of
Cinxia; but a series of black double arches along the hind margin
and the absence of rows of black spots serve to distinguish this
species from the last.

Athalia is another local butterfly, but is sometimes found in
abundance in the spots which it frequents. It is met with chiefly
in the open spaces of woods along the south coast and for some
distance inland. Devon, Cornwall, Sussex, and Kent seem to be
the most favoured counties; and London entomologists would do
well to search for it in Epping Forest.

The butterfly deposits its eggs during June and July, on several
different food plants, the chief of which are the greater and narrow-leaved
plantains (Plantago major and P. lanceolata), foxglove
(Digitalis purpurea), two species of cow-wheat (Melampyrum
pratense
and M. sylvaticum), wood sage (Teucrium Scorodonia),
and the germander speedwell (Veronica Chamædrys), and the
young caterpillars, after feeding for only a week or two, commence
their period of hybernation. They resume their feeding in April,
and change to the pupal state about the end of May.

The colour of the caterpillar is velvety black, finely dotted
with white, and the spines are yellow or orange, tipped with
white.

The chrysalis is creamy white, banded and patched with[Pg 164]
orange and black, and is suspended by anal hooks from a silken,
carpet which the caterpillar had spun on the leaf of the food
plant.

The Comma (Vanessa C-Album)

Leaving the Fritillaries, we now come to a genus (Vanessa)
that includes seven most beautiful butterflies, some of which are
so common as to be known to almost everybody.

It will be observed that this genus belongs to the same family
as the Fritillaries, and we may therefore expect to find that
the two groups possess features in common. A slight examination
of a few in their different stages will show that this is so.
Thus, the perfect insects have only four walking legs, the caterpillars
are all spiny, and the chrysalides are angular.

There is another feature concerning the chrysalides worthy of
note. Like some of the pupæ of the Fritillaries, they are adorned more
or less with brilliant metallic
spots, sometimes of
a rich golden hue, and
sometimes resembling
burnished silver. Now
the word ‘chrysalis,’
which, as we have already
seen, is derived from a
Greek word meaning
‘gold,’ was originally applied
to the pupæ of some
of the Vanessas, on account
of their metallic decorations, but it has since been extended
to the pupæ of all the Lepidoptera, and also to other orders of
insects, even though the greater number of them display no tints
of the precious metal.


Fig. 75.—The Comma—Under Side.

The first member for our consideration is the Comma Butterfly,
of which an illustration is given in Plate III, fig. 7. No one could
mistake this beautiful butterfly for any other British species, for
its wings of rich orange brown, with black and dark-brown markings,
are so irregularly scalloped on the hind margins that they
present a somewhat ragged appearance. Its name is derived
from the fact that a white mark something like the letter C, or,
as some have it, like a comma, is distinctly painted on the dark
brown of the under side.[Pg 165]

This butterfly generally emerges from the chrysalis late in the
summer—August and September, but it is often seen earlier, and
frequently as late as October. It is a great lover of sweets, and
may be found settled on various flowers and fruits. Its chief food
plants are the hop (Humulus Lupulus), red currant (Ribes
rubrum
), stinging nettle (Urtica dioica), and the Elm (Ulmus
campestris
).

It is very abundant in certain districts where hops are grown,
but seems to avoid those counties that border the sea. It is widely
distributed in the midland counties, and extends to the north of
England and into Scotland, but is very capricious in its appearance
in many parts.

The eggs are laid in May by females that have hybernated
through the winter, and the caterpillars may be found feeding
during July and August.

The caterpillar is coloured grey and brown, with a black head,
and a broad white stripe down the back of the hindermost segments.
The body is armed with a number of spines, some of which are
white, and others pale brown.

The chrysalis is a very peculiar object, having two ear-like projections
extending forwards from the sides of the head. It has a
number of angular projections, and is of an umber-brown colour,
finely netted with black lines, and having several spots of a brilliant
metallic lustre.

The Large Tortoiseshell (Vanessa Polychloros)

Our two tortoiseshells—large and small—are very similar in
their colour and markings, and moreover are not always to be
distinguished by their size, for specimens of the larger species are
sometimes even inferior in this respect to the largest of the smaller
species; so, to avoid all risks of mistaken identity, we must look for
more reliable marks of distinction between them.

The present species is figured on Plate III (fig. 8), where it will
be seen that the ground colour of dark tawny brown is spotted and
bordered with black. The border of the hind wings contains a row
of crescent-shaped blue spots. The costal margin of the fore wings,
between the black patches, is decidedly lighter than the general
ground, and is yellow rather than brown. It will be noticed,
too, that a black spot lies very near the anal angle of these
wings.[Pg 166]

The under surface, though by no means brilliant, exhibits a rich
blending of various shades of brown.

This butterfly is not known to occur in either Scotland or
Ireland, and is by no means common in England. Its chief localities
are in the midland and eastern counties.

The perfect insect generally appears about the middle of July,
and after spending a month or six weeks on the wing, seeks out a
sheltered spot in which to spend the winter. In the spring—April
or May—it again takes to flight, and during the latter month the
females are busily engaged in the deposition of their eggs.

The caterpillar feeds on the two species of elm (Ulmus campestris
and U. montana), willow (Salix alba), sallow (S. Caprea),
osier (S. viminalis), aspen (Populus tremula), and certain fruit
trees; and is full grown about midsummer. It is of a tawny grey
colour, with a black stripe on each side, and is covered with very
small wart-like projections, and the spines are branched.

The chrysalis is of a dull pinkish colour, and may be found on
tree trunks, palings, and walls, about the end of June, suspended
from a silken carpet by means of its anal hooks.

The Small Tortoiseshell (Vanessa Urticæ)

Urticæ (Plate III, fig. 9) may be distinguished from Polychloros
by the absence of the black spot in the anal angle of the fore wings
of the latter. It has also a white spot near the tip of each fore
wing-between the black border and the first black costal patch.
The whole of the base of the hind wing is also black, and the ground
colour is decidedly brighter.

It is one of the commonest of all British butterflies, and is to be
found more or less abundantly in nearly all parts of the British
Isles.

The hybernated perfect insects come out early in the spring, and
lay their eggs in close irregular clusters on nettles (Urtica dioica
and U. urens). Shortly after the gregarious caterpillars may be
found on these plants in dense masses. They change to the
chrysalis state about the end of May, and from this time there is a
continuous succession of butterflies till the end of the summer.

The later specimens, which do not emerge till September or
October, spend only a short time on the wing, and then hybernate
till the spring, giving rise to the first brood of the following season.

The caterpillar of this species is black above and greyish beneath.[Pg 167]
It is thickly covered with yellow dots, which are so close together
on the back as to form two yellowish stripes, separated only by a
fine black line. There are also two yellowish stripes along each
side; and the body, as with the rest of this genus, is spiny, the
spines in this case being black or very dark green.

The chrysalis is brownish, and spotted with burnished gold in
variable quantity—sometimes so plentifully as to cover the greater
part of the surface.

The Peacock (Vanessa Io)

This is another of our commonest and most beautiful butterflies.
Its general appearance is such that it cannot possibly be mistaken
for any other. The upper side (Plate IV, fig. 1) is rendered conspicuous
by the beautiful eye-like marks at the costal angles of all
four wings; and the under surface is very richly decorated with a
fine arrangement of black and dark-brown patches and streaks.

Io is very abundant in all parts of England, and is well known
in many parts of Scotland and Ireland, but seems to be rare in the
extreme north of both of these countries.

Its food plant is the stinging nettle (Urtica dioica), and on this
the eggs are laid in April by females that have hybernated during
the winter.

The caterpillar is full grown at the end of June or beginning of
July. It is black, with numerous minute white wart-like projections.
Its spines also are black, and its claspers brown.

The chrysalis may be found suspended by the tail on some
object in the neighbourhood of the food plant, or sometimes on the
food plant itself. It is of a greenish colour, with yellowish patches,
but turns darker as the time approaches for the emerging of the
perfect insect.

This event takes place in August, and the butterfly, after a brief
period on the wing, seeks out a sheltered spot for its winter nap.

The Camberwell Beauty (Vanessa Antiopa)

The reader will be fortunate if he succeeds in netting a specimen
of this highly prized British butterfly. It derives its popular name
from the fact that a few were taken in Camberwell about a hundred
and fifty years ago; and since that time it has been seen and taken
in variable numbers in several parts of England. So widely distributed,[Pg 168]
indeed, are its localities, and so few, comparatively, its
appearances, that it would be useless to attempt to give any hints
as to where it may be looked for. It is, however, a very common
butterfly in many continental countries, and foreign specimens may
be obtained from any dealer in entomological wares for a few pence
each.

This rare British gem is illustrated in fig. 2 of Plate IV. Here
it will be seen that nearly the whole of the surface is covered with
a rich velvety purple brown, bordered with a black band containing
blue spots; and outside this is a border of white, finely dotted and
streaked with black. The continental specimens may be easily distinguished
from the genuine Britishers by a darker border with a
decidedly yellow tinge.

The eggs of this species are generally laid on the young leaves of
the willow (Salix alba), in the spring, by females that have hybernated,
but sometimes the nettle (Urtica dioica) and the birch
(Betula alba) are selected for the food of the larvæ.

The caterpillar is black and spiny, and has a row of seven rather
large reddish-brown spots on the back, commencing at the fifth
segment.

The chrysalis, like those of the other members of this family,
is angular and suspended by the ‘tail.’ The perfect insect appears
in August, and may be seen from that month till October.

The Red Admiral (Vanessa Atalanta)

There seems to be a tendency with many to under-estimate the
beauty of certain natural objects because they happen to be so very
common, and this is particularly the case with some of our most
familiar butterflies. The beautiful Red Admiral (Plate IV, fig. 3)
may possibly suffer in this respect; for, not only is it one of the
commonest of our butterflies, but it fearlessly hovers among the
flowers of our gardens, often venturing into the very heart of thickly
populated towns.

The bright scarlet bands and white blotches of this gorgeous
insect stand out boldly on the rich velvety black ground of the
wings, and the additional touches of blue in the anal angles of the
hind wings add to the effect. The under side of the fore wings is
somewhat similar to the upper surface, but is relieved by brown
and blue; and this side of the hind wings presents most beautiful
and indescribable blendings of various shades of brown, grey, and[Pg 169]
pink. The female may be distinguished by the presence of a small
white spot on the scarlet band of the fore wing.

The eggs are deposited singly on the nettle (Urtica dioica) in
spring by females that have hybernated through the winter.

The caterpillar always feeds under the cover of a tent made by
drawing leaves together. It is spiny, and its colour is usually a
greenish or yellowish grey, spotted with black, and striped along
the sides with white or yellow. When fully grown it bites the stem
of the nettle nearly through a few inches from the top, so that the
upper part of the plant bends over the withers. It then constructs
a commodious tent by binding the leaves of this drooping portion
together, and suspends itself from the roof of this strange home to
undergo its metamorphoses.

The change to the chrysalis state takes place in July or August,
and the perfect insect may be seen during August, September,
and October in almost every part of the British Isles.

The Painted Lady (Vanessa Cardui)

Although the time of appearance of this butterfly generally
corresponds with that of the last species, yet it is exceedingly
variable, so much so that it is impossible to give any fixed period
as its season. It is, moreover, very capricious with regard to its
localities and its numbers. Sometimes it will turn up unexpectedly
in positive abundance in certain localities where
previously it had been a mere straggler; and then, for some
unaccountable reason, become comparatively scarce for several
successive seasons.

The upper surface of this beauty (Plate IV, fig. 4) is adorned
with pale red, orange, and black, and with five white spots near
the tip of each fore wing. The under side of the fore wings is
marked something like the upper, but much of the black is replaced
by shades of brown. The hind wings are beautifully variegated
beneath with greys and browns, and have a row of eye-like spots
near the hind margin.

The eggs of this butterfly are laid singly on various species of
thistles, particularly the common field thistle (Cnicus arvensis),
generally in the month of June.

The caterpillar, which is black above and red beneath, with
yellowish stripes along the back and sides, feeds under the cover of a
silken web which it constructs among the leaves. It is full grown[Pg 170]
in July or August, when it suspends itself after the manner of the
other Vanessas previous to undergoing its changes.

The chrysalis is angular, coloured with brown and grey, and
adorned with brilliant gold spots.

The perfect insect may be seen at large throughout late summer
and the autumn, and the eggs are laid by females that survive the
winter.

The White Admiral (Limenitis Sibylla)

The White Admiral (Plate IV, fig. 5) is neither so pretty nor so
common as its red namesake, but it is nevertheless a fine insect,
although the chief beauty is reserved for the under surface. Above,
the ground colour is a very dark rusty brown, relieved by bands
and spots of white. The under surface is beautifully marked with
silvery blue, bright orange brown, and white, the latter being
arranged just like the corresponding colour on the upper side.

It will be observed that this butterfly does not belong to the
Vanessa genus; so, while we may look for family resemblances,
we shall observe a few features in which it differs from the preceding
species.

It is not by any means abundant, being unknown in Scotland
and Ireland, and confined in England almost exclusively to the
oak woods of the south, where its food plant—the honeysuckle
(Lonicera Periclymenum)—abounds. Here it may be seen during
July, gracefully sailing among the trees and across the open spaces.

The caterpillar is very different from those of the Vanessas.
Its colour is dark green, with a narrow white stripe along each
side. There are very conspicuous branched spines on the third and
two following segments, also on the eleventh and twelfth; and
smaller spines on most of the others. All the spines are of a
brownish colour, with pink tips. While it is yet very small it prepares
its winter quarters by bending round the remains of a leaf on
which it has been feeding, securing the edges by silken threads,
and then binding it to the stem of the plant. Soon after, the petiole
becomes detached from the stem, and the little caterpillar then
rests suspended in its snug swinging cradle, where it remains
perfectly secure till the following April, when the warm sun calls
it out to feed on the opening leaves. It continues at this till about
the beginning of June, and then changes to a beautiful angular and
eared chrysalis, of a bright green colour, marked with brown, and
having brilliant silvery spots and streaks.[Pg 171]

Family—Apaturidæ

The Purple Emperor (Apatura Iris)

This grand insect is the only British member of its family, and
richly deserves its popular title. The male, which is figured on
Plate V (fig. 1), exhibits a most gorgeous imperial purple, which is
reflected at certain angles only from the upper surface of his large
and powerful wings. His flight is lofty and vigorous, and among
the topmost branches of majestic oaks, where he defies the efforts
of would-be capturers. Unlike our other butterflies, he is also a
very quarrelsome creature, and will not hesitate to fiercely attack
a brother Emperor who dares approach the branch he has selected
for his throne.

Many attempts have been made to capture this prized creature
by means of a large net mounted on the end of a pole twenty or
thirty feet in length, but the wielding of such a cumbersome implement
against so powerful an insect is no mean task, and but few
fall a prey to such a snare. But it so happens that this imperial
personage has a very depraved appetite, the indulgence in which
has often brought him to ruin. Instead of searching out the sweets
so bounteously supplied by the blossoms that are so attractive to
other lepidopterous insects, he delights in sipping the waters of the
filthiest puddles, and imbibing the odoriferous moisture of dung and
the decomposing carcases of animals. So deeply seated is this depravity
of taste that the Emperor may be netted with ease while
indulging in his sumptuous feast, and is even to be taken at times
with the fingers.

The knowledge of this peculiarity of the imperial palate has led
entomologists to abandon the awkward net, and to bait the woods
with viands that alone can entice his highness from his lofty seat;
and many a splendid specimen has been easily captured while
enjoying the luxurious juice of a dead cat, stoat, or rabbit, or of a
seething mass of pig’s dung.

The female is larger than her mate, and does not display the
beautiful purple reflections that adorn the male. She is very
different, too, in her habits, for she sits nearly all day on high
branches of trees, giving her attention to the graver duties of an
imperial mother, and is consequently but seldom seem. She lays
her eggs in July on the sallow (Salix Caprea) or the poplar (Populus),
and in less than a fortnight the young caterpillars are hatched.[Pg 172]
They feed on till the leaves are falling, and then fix themselves by
their claspers to a silken carpet which they construct on a twig. Here
they remain, exposed to all the wintry blasts and frosts, till the new
leaves are out in the spring, when they again commence feeding, and
continue to do so till they are full grown—in May or June.



Fig. 76.—The Purple Emperor—Under Side.

The under side of this species is shown in fig. 76, in which will
also be observed the eye-like spots of the fore wings which have
given rise to its specific name (Iris).

The caterpillar (Plate VIII, fig. 5) is a very peculiar creature.
Its body is green, with seven oblique yellowish stripes on each
side, and it has a pair of horns attached to its head.

The chrysalis (Plate VIII, fig. 10) may be found in June, suspended
to the under side of a leaf. It is of an apple-green colour,
and still exhibits the oblique stripes which we observed in the
caterpillar.

This insect is not to be found in either Scotland or Ireland, but
is more or less abundant in many of the oak woods of the midland
and southern counties of England. Among the numerous favoured
localities, we may mention Colchester, Forest of Dean, Northamptonshire,
Ipswich, Huntingdonshire, Buckinghamshire, Epping,
Lyndhurst, and the Isle of Wight.[Pg 173]


CHAPTER XIV

THE BROWNS AND HEATHS

Family—Satyridæ

This family contains eleven British species, often spoken of
collectively as the ‘Browns,’ since in most of them the prevailing
tints are various shades of brown. They are decidedly dingy in
comparison with the beautiful butterflies we have been previously
observing; but to this statement we must allow one marked
exception, for the family includes the beautiful Marbled White,
which stands out prominently among its fellows for brilliancy and
boldness of colour.

The caterpillars of the ‘Satyrs’ have no spines, but their bodies
are covered with very minute hair-bearing warts that give them a
soft velvety appearance. The hinder extremity tapers off considerably,
and terminates in two points.

The chrysalides are not angular like those of the preceding
species, and though generally suspended by the tail, are sometimes
found quite free among leaves and grasses on the ground.

The perfect insects are rather feeble fliers, and generally take so
little notice of intruders that they are easily caught in the hand.
Their wings are devoid of angles, and they have only four perfectly
developed legs.

The Marbled White (Melanargia Galatea)

Our first member of this family is the exception to which we
have already alluded as a relief to the general dinginess of the
‘Browns.’ Its colours above are cream and black, arranged
as shown in Plate V, fig. 2. The under side (fig. 77) is marked
with white, black, and greenish grey, with a row of eye-like
spots parallel with the hind margin of the hind wings.[Pg 174]



Fig. 77.—The Marbled White—Under
Side.

This butterfly is not known in Scotland or Ireland, nor is it to
be found in several of the northern counties of England. Its chief
haunts are the waste cliffy grounds of the southern and some of
the midland counties of England, where it is usually restricted to certain
small districts. In some places it is really a common insect,
and among these may be mentioned Brighton, Horsham, Dover,
Folkestone, Margate,
Gravesend, New Forest,
parts of Gloucestershire,
Cambridgeshire, and
Devonshire, also in the
Isle of Wight and South
Wales.

The perfect insect is
out in July, during which
month the eggs are deposited
on various grasses,
or indiscriminately on
leaves and stems in grassy
spots.

The caterpillar feeds on grasses; and, being still small at the
end of the autumn, hybernates during the winter among the stems of
grass. It feeds again in April, and is fully grown by the end of May.
Its colour is a dull green or brownish, with a darker stripe down
the back, and lighter stripes along the sides. Its spiracles are black.

The chrysalis is pale brown, marked with lines of a slightly
darker shade. It may be found among grass stems, without any
attachment, during the month of June.

The Small Ringlet (Erebia Epiphron)

On account of the very limited range of this butterfly, only those
who have the opportunity of visiting its haunts can have any
practical acquaintance with its natural history. It is almost
exclusively confined to the lake district in England, to a few
mountainous localities in Scotland, and to one or two similar
localities in Ireland. Its strong partiality for elevated situations
has earned for it the popular name of Mountain Ringlet.

The colour of the upper surface (Plate V, fig. 3) is a dark
brown, with a broad band of rusty brown, parallel with the hind
margin of each wing, and broken by the wing rays. Each division[Pg 175]
of these bands has often a black central spot, but frequently these
are entirely absent. The colouring of the under side is very
similar but less defined, and the rusty spots of the hind wings are
very small.

The butterfly is out in June and July. The caterpillars, which
are green, with white stripes along the sides, feed on various
grasses. They hybernate during the winter, and change to the
chrysalis state in the following May or June.

The Northern Brown (Erebia Æthiops)

The colour of this species (Plate V, fig. 4) is a rich dark brown,
with rust-coloured and black spotted bands arranged something
like those of the last. The markings, however, are very variable.
There are usually four black spots on the band of the fore wings,
but the first two of these are always united, and centred with
white. The third is often very small or entirely wanting.

The under side of the fore wings is marked something like the
upper, but the hind wings on this side are grey, with two broad
bands of a darker colour.

As its popular name implies, this butterfly is a northerner. It
is common in Scotland, where it flies in elevated spots. In
England it is confined to the mountainous districts of the
north.

The perfect insect is at large in July and August, during which
time the eggs are deposited on various grasses or on low-growing
herbage in grassy spots.

The caterpillar is of a brown colour, and has a narrow black
stripe down the middle of the back, and two other stripes, lighter
than the ground colour, one on each side. At about the end of
June it turns to a chrysalis of a brownish colour.

The food plants of this species include a number of common
grasses.

The Speckled Wood or Wood Argus (Pararge Egeria)

Most of our butterflies delight in the hot sun, and are to be
seen on the wing only when it is shining brightly. This fact is
particularly noticeable on a bright day with occasional heavy
clouds. While the sun’s rays are pouring uninterruptedly on the
landscape, numbers of these light-lovers are to be observed flitting[Pg 176]
about; but when the dense shadow of a passing cloud creeps over
the ground they rapidly disappear from view, having settled down
to rest on leaves and stems. Then, as soon as the shadow passes
away, the air is again enlivened with their sports and flittings.

The Wood Argus is a marked exception to this rule. It
delights in the cool shade of the narrow paths of woods, where it
slowly flies up and down the lonely footpath, taking but little heed
of strangers that intrude on its haunts, and seldom venturing into
the full blaze of the sun unless pursued. Even on dull days it
continues its solitary flight, and may even be seen on the wing
while a soft rain is bathing the dripping foliage.


Fig. 78.—The Wood Argus—Under
Side.

The upper surface of this pretty butterfly is shown on Plate V,
fig. 5, and the under side in the accompanying woodcut. Both
sides are prettily marked with various shades of brown and buff,
and adorned with white-centred
dark eye-spots which have earned
for it the name of Argus.

It first appears on the wing in
April, and may be seen from this
month continuously to the end of
August.

The food plants probably consist
of many species of grasses, the
cock’s-foot (Dactylis glomerata)
and couch grass (Agropyron repens)
being among the number, and the
eggs are laid on or in the neighbourhood of these during the summer
months.

The caterpillar of this species is of a dull greenish or brownish
colour, and it has two whitish stripes (sometimes three) down the
middle of the back, and similar stripes along each side. It
hybernates during the winter, and is full grown in March, when it
changes to a dull green or brownish chrysalis, which is streaked
with black, and has a few white dots on the back.

It has been stated that the butterfly is on the wing from April
to August, and, according to some authorities, there are no less
than three broods during this time, following each other in rapid
succession. It is common throughout England and Ireland, and is
known in parts of Scotland.[Pg 177]

The Wall Butterfly (Pararge Megæra)

Belonging to the same genus is another very familiar butterfly
—the Wall—which receives its popular title from its peculiar habit
of frequently resting on walls and stony banks. It is one of the
first, if not the first, to take to the wing in the morning, and is
generally the last to seek its hiding place in the evening. I have
seen it actively flying about during August, as early as 7.30 in the
morning, and found it still flitting from one spot to another along
the western side of a wall as late as 8 in the evening, as if in search
of a convenient shelter for the fast approaching night.

This pretty ‘Brown’ must be familiar to the reader, and the
coloured drawing on Plate V (fig. 6) will at once serve for purposes
of identification without the necessity of a wordy description. It
may be mentioned, however, that the male (the sex figured) is
smaller than the female, and is further distinguished by a broad dark
oblique band passing across each fore wing.

The Wall is a double-brooded butterfly, the first brood appearing
in May, and the second in August. The caterpillars which produce
the latter may be found on the cock’s foot (Dactylis glomerata)
and other grasses in June, while those of the former are hybernators;
and the chrysalides of the two broods may be found in April
and July respectively.

The colour of the caterpillar is green, with a slightly darker
stripe down the middle of the back, a pale stripe along each side,
and another similar stripe about midway between these two.

The chrysalis is green with the exception of the more prominent
parts of its surface, which are almost white.

This species is very common in almost every locality in Britain.

The Grayling (Satyrus Semele)

The Grayling is the largest of our ‘Browns,’ and, although a
powerful flier, it seldom takes long flights. The female, which is
shown in fig. 7, Plate V, is really a beautiful creature, the light
markings of which stand out in bold contrast with the deep brown
ground colour; but the male is comparatively dingy, there being
much less contrast between the ground and the markings. He is
also smaller than his mate.



Fig. 79.—The Grayling—Under Side.

The under side of both sexes is similar (fig. 79), the pattern of
the fore wings being much like that of the other side, but considerably[Pg 178]
lighter, and the hind wings are beautifully marbled with various
greys and browns.

This species is not nearly so common as the two preceding, but
it is very widely distributed, and is exceedingly abundant in some
parts. On some of the heathery cliffs and downs of the south and
south-west coasts it is so
plentiful that the butterflies
are started into the air at
almost every step, for it
seldom flies except when disturbed.
It is a common
insect in Ireland, and also in
parts of Scotland.

The caterpillar is a hybernator,
and may be found
feeding on grasses in the
autumn and the spring. It
changes to the chrysalis in June, and the perfect insect is on the
wing from June to the beginning of September.

The colour of the caterpillar is pinkish drab above, and greenish
drab beneath. A dark brown stripe, edged with a lighter colour,
passes down the middle of the back, and a dark line on each side.
It changes to a dark reddish-brown chrysalis on the surface of the
ground, or, according to some observers, a little beneath the surface.

The Meadow Brown (Epinephele Janira)

Although this very common butterfly is usually considered to be
the dingiest of its family, yet it must be admitted that the colour of
a freshly emerged specimen is really very rich.

The male is of a dark brown colour, with an indistinct patch of
a lighter tawny brown near the outer margin of the fore wings, and
a white-centred black eye-spot near the costal angle of the same
wings. The female (Plate V, fig. 8) is of a lighter colour, the eye-spot
on her fore wings is larger and far more conspicuous, and an
irregular patch of light orange brown occupies a large area of each
of the same wings. She is, moreover, larger than her mate, and in
every way a more attractive insect.

The Meadow Brown abounds everywhere, from June to September,
and may be seen on grass land and waste grounds where
other butterflies are seldom found.[Pg 179]

The caterpillar is green, and is rendered slightly rough by a
number of minute warts. There is also a white stripe on each side.
It feeds on various grasses in the autumn, hybernates during the
winter, and is full grown in May.

The chrysalis is apple green, spotted with a lighter green, and
has several black markings.

The Large Heath (Epinephele Tithonus)

This butterfly is sometimes called the ‘Small Meadow Brown,’
and is certainly much like the last species, both in colouring and
habits.

The fore wings of the male (Plate V, fig. 9) are light orange
brown, bordered with dark brown, and having a broad patch of the
same across the middle; and near the costal angle is a round black
spot with two white dots.
The hind wings are dark
brown with a patch of light
orange brown near the centre,
and a small eye-spot near the
anal angle. The female is
exactly similar, except that
she does not possess the broad
bar on the fore wings.



Fig. 80.—The Large Heath—Under
Side.

The under side is shown
in fig. 80, and is coloured
with various shades of brown.

This is a very common butterfly, and may be seen during July
in most English counties, also in the south of Scotland, and in a
few localities in the south of Ireland. It frequents meadows,
heaths, downs, and lanes, like Janira, but is not nearly so abundant
as that species.

The young caterpillar is hatched in August, and is still very
small when it seeks its winter shelter among the stems of grasses.
It resumes feeding in the following May, and is full grown towards
the end of June. Its colour is very variable—pale green, olive
green, or dull brown, with five longitudinal stripes at about equal
distances from each other. These consist of a dark one down the
middle of the back, a pale line along each side, and another pale
line midway between these.

The chrysalis may be found at the end of June, attached by[Pg 180]
the tail to blades of grass. It is of a very light colour, almost
white, but adorned with numerous black lines and patches.

The Ringlet (Epinephele Hyperanthus)


Fig. 81.—The Ringlet—Upper Side.

This is another rather plainly dressed insect, though somewhat
prettily adorned on the under side. The upper surface is of a very
deep sepia brown, almost black, with a few indistinct black eye-like
spots near the margins. The under side (Plate V, fig. 10) is of a lighter
umber brown, with corresponding eye-spots generally very conspicuous.
These spots are black, with white centres, and generally
surrounded by light rings. They are subject, however, to considerable
variation. Those on the upper surface are sometimes quite
absent in the male, but are nearly always readily perceptible in the
female. On the under side, too, they are occasionally quite absent,
while in other varieties they
are minute white-centred
dots, without any surrounding
light ring. Our coloured
drawing represents the most
usual form.

The favourite haunts of
the Ringlet are the borders
of woods, and the sheltered
sides of flowery hedgerows.
It is not so widely distributed
as some of the common
‘Browns,’ but is usually very abundant where it occurs, sometimes
appearing in such numbers that several may be taken with a single
stroke of the net. It does not seem to be a frequenter of Scotland,
and is known in Ireland only in the south. Its head quarters are
the southern and south-midland counties of England.

The eggs are laid in July on various grasses, on which the young
caterpillars feed from about the middle of August till the cold weather
sets in. They hybernate at the roots of the grasses till the beginning
of the following May, and change to the chrysalis state about
the middle of June, suspending themselves to grass blades by
means of their anal hooks.

The colour of the caterpillar is dull green or brown, and is
marked with five longitudinal stripes much like those of the
Large Heath.[Pg 181]

The chrysalis is pale brown, spotted and striped with a darker
shade of the same colour.

The Marsh Ringlet (Cænonympha Typhon)


Fig. 82.—The Marsh Ringlet—Under
Side.

The upper surface of this butterfly is shown in the first figure
of Plate VI, and the under side in the accompanying woodcut;
but it must be remembered that the species is a very variable one,
so much so that it is almost impossible to give anything like a short
and, at the same time, a satisfactory description. The female may
usually be distinguished by a pale patch across the middle of the fore
wings; and the eye spots of the same wings, always more or less
indistinct when present, are sometimes entirely wanting. The
markings of the under side are even more variable, the transverse
bars and the eye spots being often
particularly conspicuous, and at
other times hardly discernible.

This is generally spoken of as a
northerner, its chief localities being
in the mountainous parts of Scotland
and the elevated districts of
the north of England, but in Ireland
it extends to the southern
ranges. Its haunts are elevated
moors and marshy heaths, where
its food plant—the beak-rush (Rhyncospora alba)—abounds, and it
is on the wing from the end of June to August or September.

The caterpillar is green, with five longitudinal stripes—one dark
one, bordered with yellow, down the middle of the back, and two
pale yellow ones on each side. It is a hybernator, and is full grown
about the end of May, when it suspends itself by the hindmost
claspers to a silken carpet, and changes to a green chrysalis with
pale brown wing cases.

The Small Heath (Cænonympha Pamphilus)

The last member of the family Satyridæ is the well-known Small
Heath, that may be seen almost all over the British Isles on heaths,
meadows and moors, from May to September.

The upper surface of this butterfly (Plate VI, fig. 2) is a tawny
yellow, with a dark brown border, and a spot of the same dark tint[Pg 182]
near the tip of each fore wing. The under side is much like that
of the last species, but there are no eye spots on the hind wings.

The eggs of the first brood are laid during May and June on the
various grasses on which the caterpillar feeds.

The caterpillars that emerge from these are fully grown in July or
early August, and go through their changes during the latter month;
but the later ones hybernate during the winter, and are not full
fed till the following May.

The colour of the larva is pale apple green, with a wide darker
stripe down the back, two others along the sides, and two more
between the latter and the dorsal stripe. All these five stripes are
bordered with a whitish colour.

The chrysalis is bright apple green, dotted with white, and the
wing cases are striped with a purple-brown line edged with white.[Pg 183]


CHAPTER XV

THE HAIRSTREAKS, COPPERS AND BLUES

Family—Lycænidæ

This is a large family, including as it does no less than nineteen
of the British species. These are all of small size, and are characterised
by their short and jerky flights. They seldom rise much
above the ground, and are consequently very easily caught.

The caterpillars of this family have all short and rather thick
bodies, shaped very much like that of the wood louse—flattened
beneath and very convex above.

The chrysalides are generally attached by the ‘tail,’ and further
secured by a silken cord round the body, as we have already observed
in the case of the Pieridæ.

The perfect insects differ from the preceding species in that all
six legs are perfectly developed and adapted for walking.

There are only three genera in this large family:

  1. Thecla—The Hairstreaks, with ‘tailed’ wings.
  2. Polyommatus—The ‘Coppers.’
  3. Lycæna—The ‘Blues,’ with wings either blue or brown.

The Brown Hairstreak (Thecla Betulæ)

The five Hairstreaks which constitute the genus Thecla are all
pretty insects, characterised by hair-like streaks on the under
surface.


Fig. 83.—The Brown Hairstreak—Male.

Betulæ is the largest of these. Its upper surface is of a deep
brown colour, with orange-brown marks at the anal angles of the
hind wings, and, in the female, a large patch of orange on the fore
wings. The under side (Plate VI, fig. 3) is orange brown, much
lighter in the male than in the female. On the fore wings are two[Pg 184]
white lines, the inner one of which is indistinct; and on the hind
wings are two others, the outer one being longer and more distinct
than the inner.

This butterfly is by no means an abundant insect, though it is
widely distributed, and in some places
plentiful. Its chief haunts are woods,
and we may mention among its
favoured localities Epping Forest,
Monk’s Wood in Cambridgeshire, the
wooded parts of South Devon and
Dorset, New Forest, Colchester, and
Peterborough.

The perfect insect is on the wing
from July to October, and the eggs are
deposited in the autumn on the twigs
of its food plant—the blackthorn
(Prunus spinosa). These do not hatch till the following spring.
Toward the end of June the caterpillar is fully fed.

The colour of the caterpillar is light green, with two white stripes
down the back, and two others along the sides. There are also two
small oblique whitish lines on each side of each segment.

The chrysalis is smooth, and of a pale brown colour.

The Black Hairstreak, or White-letter Hairstreak
(Thecla W-album)


Fig. 84.—The White-letter
Hairstreak.

The first of the above two popular names has been applied to
this species on account of the very deep brown colour of the upper
side, which colour is often a near approach
to black. The second is due to the W-shaped
bend of the white streak of the hind wings.
The ground colour of the under side (Plate
VI
, fig. 4) is greyish brown, with a bright
orange band, spotted with black near the
hind margin of the hind wings.

W-album is a somewhat rare insect, but
is occasionally seen in plenty in a few localities,
Cambridgeshire, Berkshire, Epping,
Colchester and Suffolk being among its chief resorts. It is out
on the wing in July, and should be looked for in wooded country
where the common elm (Ulmus campestris) and the wych elm
(U. montana), its food plants, exist.[Pg 185]

The eggs are laid on the twigs of these trees late in the summer,
and the young caterpillars do not appear till the following spring.
The chrysalis may be found attached to an elm twig or leaf about
the end of June.

The caterpillar is pale green. The ridges along the back are
tinged with yellow, and there are two fine oblique white lines on each
side of each segment.

The Dark Hairstreak (Thecla Pruni)

The upper side of this butterfly is very much like that of
W-album, but it may be distinguished by the presence of a few
orange spots near the anal angle of the hind wings. The colouring
of the under side (Plate VI, fig. 5) is also very similar, except that
the white lines of the wings are thinner and less distinct than in the
last species, and do not exhibit the W-shaped bend. The orange
band of this surface is bordered on each side with a row of black
spots, each of which is touched with a bluish white or a metallic
blue.

This insect is not by any means common, but has been seen in
considerable numbers in certain localities. It is not found in
either Scotland or Ireland, and its chief haunts in England seem
to be in Huntingdonshire, Cambridgeshire and Northamptonshire.
It frequents wooded country, and flies during June and July.

The eggs are laid late in the summer on the twigs of the blackthorn
(Prunus spinosa), and are not hatched till the following
spring.

The caterpillar, which is pale green, with rows of yellow spots,
may be found in May.

The Purple Hairstreak (Thecla Quercus)


Fig. 85.—The Purple
Hairstreak—Male.

This pretty butterfly, by far the commonest of the Hairstreaks,
though comparatively very small, reminds one forcibly of the noble
Purple Emperor. Its haunts are the same oak woods, and its upper
surface, though only a dull dark brown in certain lights, exhibits
the same imperial purple reflections when viewed at certain angles.
The purple of the male extends over the whole of the wings, but
that of the female is confined to a V-shaped patch at the base of
the fore wings. In the latter case, however, the purple is much
richer than in the male sex.[Pg 186]

The under side (Plate VI, fig. 6) is coloured with a delicate
grey ground, adorned with a white streak on each wing, and a
couple of orange spots near the anal angle of the hind wings.

This species is very widely distributed,
being common in oak woods
in most parts of England, and also in
many parts of Scotland and Ireland.
It flies around the branches of the
trees, and often disappoints the collector
by keeping far beyond the reach
of his net.

Those in search of this pretty insect
should ramble in oak woods, preferably
in the south of England, during July
and August. The eggs may be found glued to the twigs throughout
the winter, and the larvæ may be beaten from the branches of the
oak in June.

The colour of the caterpillar is brownish or pinkish green, with
a row of V-shaped marks down the back.

The chrysalis is of a brown colour, short and thick, and may be
found either attached to oak leaves, or under the surface of the
earth at the foot of the tree on which the caterpillar fed.

The Green Hairstreak (Thecla Rubi)

Next to Quercus, this is the most plentiful of the genus. It
frequents woods and heaths in nearly every county in England, and
is also found in parts of Scotland and Ireland. It is peculiar
among British butterflies as being the only
one that exhibits a bright green colour. It
also differs from the other Hairstreaks in two
important particulars, for the hind wings,
though angled at the hind margin, are not
‘tailed,’ and the characteristic hairstreak
which gives the popular name to the genus is
here represented only by a series of white
dots across the wings, or, in some cases, by
one or two dots on the hind wings only.


Fig. 86.—The Green
Hairstreak.

The upper side is dark brown, displaying metallic reflections
when viewed in a strong light. The under side is represented in
fig. 7 of Plate VI.[Pg 187]

The chief food plants of this species are the bramble (Rubus
fruticosus
), the birch (Betula alba), and the broom (Cytisus
scoparius
).

The perfect insect flies in May and June, and the eggs are
deposited during the latter month on the above plants. The
caterpillars are full fed in July, and change to the chrysalis state
towards the end of the summer.

The colour of the caterpillar is pale green, with a yellow stripe
and several white oblique lines along the sides, also a yellowish
stripe down the back.

The chrysalis is short and thick, and of a dark brown
colour.

The Large Copper (Polyommatus Dispar)

Our next genus contains only two British species. The first of
these—the Large Copper—was once a common insect at Whittlesea
in Cambridgeshire, and in some of the fens of Huntingdonshire,
but is now feared to be quite extinct, as none have been seen for
many years. The last capture was made in 1847 in Huntingdonshire.
However, it may turn up again; and even if it does not, it would
be a pity to allow the memory of so fine an insect to die out; so
we find room to figure it (Plate VI, fig. 8), and append a few
remarks.

There is a very great difference between the male and the
female. The former is of a brilliant copper hue, and all the wings
have a black margin and a black streak near the middle. The female
is larger; and the coppery colour is much redder. The black border
of the fore wings is wider, and there are also several large black
spots on these wings. The hind wings are almost entirely covered
with black, with the exception of a broad coppery band near the
hind margin.

The food plant of the caterpillar appears to have been the water
dock (Rumex Hydrolapathum), on which the eggs were laid late
in the summer. It is probable that the caterpillar was a hybernator,
seeking its winter shelter while still very young; and it was
full fed in June.

Its colour was green, with a darker stripe of the same colour on
the back; and the chrysalis was attached by anal hooks and a cord
round the body.[Pg 188]

The Small Copper (Polyommatus Phlæas)

The only other British member of the genus Polyommatus—the
Small Copper—is one of the commonest of our butterflies. It may
be found in nearly all parts of the British Isles from April to September,
more particularly in April, June, and August, for it is
apparently triple brooded.

This brilliant and lively little insect is shown on Plate VI
(fig. 9), and, being so very familiar, needs no description.

The caterpillar feeds on different species of dock—the broad-leaved
dock (Rumex obtusifolius), the fiddle dock (R. pulcher),
the sorrel (R. acetosa), and the sheep sorrel (R. acetosella); also on
the ragwort (Senecio Jacobæa). It is full fed about three weeks
after hatching, and then changes to a small and stout chrysalis, of
a pale brown colour, on the leaf of its food plant.

The caterpillar itself is green, with a reddish line on the back
and on each side; and it glides over the surface of the leaves something
after the manner of a slug, without exhibiting any very
apparent motion of its short legs and claspers.

The Tailed Blue (Lycæna Bætica)

We now come to a genus containing no less than ten species of
beautiful little butterflies, known commonly as the ‘Blues;’ but
one of them exhibits no trace of the colour so characteristic of the
group, although it resembles the others in structure and habits.


Fig. 87.—The Tailed
Blue—Under Side.

Our first example is the Tailed Blue,
known also as the Pea-pod Argus. The upper
side of this insect (Plate VI, fig. 10) is of a
dull smoke colour, exhibiting purple-blue reflections,
which are, in the female, confined
to distinct blotches on the bases of the wings,
but in the male are less noticeable, and
extend over the whole surface. The hind
margin of the hind wings has a row of spots,
more or less distinct, and much more prominent
in the female than in the male. The under side is beautifully
marked with bands of fawn and grey, and with two spots of brilliant
metallic green in the anal angle of the hind wings.

This butterfly abounds in the countries of South Europe, where
the caterpillar feeds on the pods of certain leguminous plants; but[Pg 189]
only a few stragglers have been taken in England, so that its reputation
as a true Britisher is very uncertain. It is highly probable
that the two or three specimens caught on our south coast were
blown over from the Continent, and that the insect has never bred
on this side of the Channel.

The Silver-studded Blue (Lycæna Ægon)

The upper surface of the male (Plate VI, fig. 11) of this species
is purple blue, with a black border on the hind margins of all wings.
The female (fig. 12 of the same plate) is of a very dark smoky-brown
colour, often with a bluish tinge, and has generally a row of orange
spots near the hind margin of the hind wings.


Fig. 88.
The Silver-studded
Blue—Under Side.

The under side of both sexes is similar, and is illustrated in the
accompanying woodcut. The ground colour is bluish grey, and is
marked with a number of black spots
surrounded by light rings. Along the
hind margin of the hind wings is a row
of orange spots, each bordered with black
on the inner side, and with a silvery
blue on the outer.

This insect appears in July, and is
common in many dry, sandy, or chalky
spots in various parts of England, and
also in a few localities in Scotland and
Ireland. It has been reported as abundant at Darlington and in
certain localities in Lancashire, but its head quarters are undoubtedly
the chalk downs and dry gravelly banks of the southern
counties.

The caterpillar feeds on the bird’s-foot (Ornithopus perpusillus),
and is full grown towards the end of June. Its colour is yellow or
grey, with a brown dorsal stripe, a white line on each side, and
pale oblique lines near the former. About the end of June it changes
to a dull green chrysalis, with projecting wing cases.

The Brown Argus (Lycæna Astrarche)

Neither male nor female of this species exhibits any trace of
blue. The upper surface, shown in fig. 13 of Plate VI, is coloured
with a warm brown, and all four wings have a row of orange spots
near the hind margin. The fore wings have also a central black[Pg 190]
spot. The under surface, drawn on the same plate (fig. 14), is
bluish grey, with a border of orange spots on each hind margin as
on the other side. There are also numerous black spots in light
rings, the arrangement of which will be seen in the figure.

Some species of butterflies and moths are so variable in their
colouring and markings that varieties have often been mistaken for
distinct species; and, in other cases, distinct species are sometimes
so similar in character that they are looked upon as identical.

A butterfly that closely resembles the normal Brown Argus in
many points, and named Artaxerxes, has often been described as a
distinct species, but is now, I believe, recognised by most entomologists
as a constant variety of the present species.

It differs from the normal type in having a white instead of a
black spot in the centre of the fore wings, and the border of orange
spots is often very indistinct. On the under side, too, instead of
black spots in white rings, it has white spots, with little or no trace
of a black centre.

The ordinary Brown Argus is a southerner, and is particularly
abundant on the chalk downs of the south coast and the Isle of
Wight, but Artaxerxes is to be found only in Scotland and the
north of England; and it is interesting to note that, between these
northern and southern districts, intermediate varieties are to be met
with.

Again, Astrarche is a double-brooded butterfly, appearing on
the wing in May and August; while Artaxerxes is single brooded,
flying at midsummer. This fact has lent support to the opinion
that the two are distinct species; but it must be remembered that
several insects that are single brooded in one country are double
brooded in a warmer climate.

The caterpillar of Astrarche feeds on the hemlock stork’s-bill
(Erodium cicutarium). It is of a pale yellow colour, with a
brownish line on the back; and is full fed in April and July.

The Common Blue (Lycæna Icarus)

Although this pretty little butterfly is so common that it is
almost sure to be known to all who take any interest in insect life,
yet it is important to observe it carefully, since it is an easy matter
to confound it with other species of the same genus.

The upper surfaces of the two sexes are very different, that of
the male (Plate VI, fig. 15) being a beautiful lilac blue; and that of[Pg 191]
the female (Plate VI, fig. 16) a dark brown, powdered with blue at
the bases of the wings, and having generally a border of orange
spots, more or less defined, on the hind margins of all wings.


Fig. 89.—The Common
Blue—Under Side.

The under side, shown in the accompanying woodcut, is ashy
brown; warm in the female, but paler in the male. The hind
wings, and sometimes all four, are
bordered with orange spots; and this
species may be distinguished from
Astrarche by the presence of two black
spots, in white rings, near the base of
the fore wings.

There will be no need to name localities
for this insect, as it is abundant
everywhere, frequenting meadows,
heaths, and all waste places. It is
double brooded, and is on the wing continuously from May to
September, the first brood enduring from May to July, and the
second from July to the end of the warm weather.

The caterpillar is green, with a dorsal line of a darker tint, and
a row of white spots on each side. It feeds on clover (Trifolium
pratense
and T. repens), bird’s-foot (Ornithopus perpusillus),
bird’s-foot trefoil (Lotus corniculatus), and the rest-harrow (Ononis
spinosa
).

The chrysalis is short and rounded, of a dull green colour, tinged
with brown on the under surface.

The Clifden Blue (Lycæna Bellargus)

Our coloured representations of this beautiful blue (Plate VI,
figs. 17 and 18) show that here also
there is a great difference between
the male and female. The former is
a most lovely and brilliant sky blue,
bordered by a fine black line; and the
latter is a dull dark brown, with a more
or less distinct border of orange spots,
and the bases of the wings are powdered
with scales of a tint corresponding with
those of the male. In both sexes the
fringe is very distinctly barred with dark brown.


Fig. 90.—The Clifden
Blue—Under Side.

The under side (fig. 90) is similar in both sexes—greyish brown,[Pg 192]
with a border of reddish spots, and a number of black spots in white
rings, the arrangement of which is here represented.

The butterfly frequents chalky downs, chiefly in the south of
England, and seems to be unknown in Scotland and Ireland. The
Isle of Wight, and the chalky downs and banks of Sussex, Surrey,
and Kent, are its favourite localities; and even in these it is generally
very local, sometimes swarming on a grassy bank of no great extent,
when the surrounding neighbourhood, though apparently equally
suitable to its requirements, does not harbour a single specimen.
It is on the wing in May and June, and again in August.

The caterpillar is green, with two rows of yellow streaks on the
back, and a yellow stripe on each side. It feeds on the Dutch clover
(Trifolium repens), horse-shoe vetch (Hippocrepis comosa), and
various other leguminous plants.

The Chalk-Hill Blue (Lycæna Corydon)


Fig. 91.—The Chalk Hill
Blue—Under Side.

The male of this species (Plate VII, fig. 1) is readily to be distinguished
from all other members of the genus by its pale glossy
blue, but the female (fig. 2 of Plate VII) so closely resembles that
of Bellargus that it is often a somewhat difficult matter to discriminate
between them. The following, however, are a few points
worthy of observation: The upper
side of the female Corydon has the
bases of the wings more or less
sprinkled with the pale silky blue that
characterises the male; and the black
bars of the fringe are usually broader
in Corydon than in Bellargus. The
black-centred spots of the under side
are also usually more conspicuous in
the former species than in the latter.

The difficulty of identification is
increased by the fact that both these butterflies frequent similar
localities, and are often on the wing at the same time; but although
Corydon is certainly a frequenter of chalky districts, yet it
is often found plentifully in districts far removed from the chalk,
notably at Arnside in Lancashire, and in Epping Forest.

The butterfly is out in June and July. The caterpillar is green,
with two rows of short yellow streaks on the back, and a yellow
stripe on each side. It feeds on the purple and Dutch clovers[Pg 193]
(Trifolium pratense and T. repens), bird’s-foot trefoil (Lotus
corniculatus
), horse-shoe vetch (Hippocrepis comosa), and lady’s
fingers (Anthyllis vulneraria).

The Holly Blue (Lycæna Argiolus)

While all the other Blues delight to sport on low flowery banks
in the full blaze of the summer’s sun, the Holly Blue prefers to flit
among the branches of trees, often many feet from the ground.
The larva feeds on the flowers of the holly (Ilex Aquifolium) in
the spring, and on those of the ivy (Hedera Helix) late in the
summer; also on the alder buckthorn (Rhamnus Frangula); and it
is in localities where these grow that we may find this lovely Blue
sporting among the branches, or resting on a leaf with its wings
folded together, thus making itself conspicuous among the dark
foliage by exposing the pale silvery blue of its under surface.



Fig. 92.—The Holly
Blue—Under Side.

The upper sides of both the male and female are shown on
Plate VII (figs. 3 and 4 respectively), where the beautiful lilac
blue will be seen to have a border of black, wider in the latter than
in the former.

The under surface is spotted with
black, as shown in fig. 92, and has no
border of orange spots.

This is a double-brooded butterfly,
appearing first in April and May, and
then again in August. It is not at all
uncommon in the south of England,
and extends northward as far as the
Lake District, but is not found in
Scotland. It is generally distributed throughout Ireland.

The caterpillar may be looked for in June and October. It is
light green, with a line of dark green down the back.

The Mazarine Blue (Lycæna Semiargus)


Fig. 93.—The Mazarine
Blue—Under Side.

The male (Plate VII, fig. 5) is deep purple blue, with a narrow
dark-brown border, and the female (fig. 6 of the same plate) dark
brown. The under side of both sexes is light greyish-brown or
drab, with a row of black spots in white rings parallel with the
hind margin of each wing, and no reddish or orange spots.[Pg 194]

This pretty butterfly seems to have been plentiful in several
localities some years since, but has not been seen for a long time;
and it is probable that its reckless
slaughter by those who catch all
the pretty butterflies they can secure
either for ornament or for gain has
caused its name to be permanently
removed from our list of natives.

It was formerly abundant in Dorset,
Hereford, Glamorganshire, and
near Shirley, and was on the wing in
June and July, but it disappeared
from our view before a full account of its life history had been
prepared.

The Small Blue (Lycæna Minima)


Fig. 94.—The Small
Blue—Under Side.

We now come to the smallest of all British butterflies—a little
insect that measures less than one inch from tip to tip when its
wings are expanded. Its upper surface is of a dull and dark-brown
colour, the bases of the wings being dusted with blue in the case of
the male. The under side is pale drab, tinged with greenish blue
at the bases of the wings, and marked with black spots in light
rings as shown in the accompanying figure.
The upper side is represented in fig. 7 of
Plate VII.

This butterfly is on the wing in May
and June, and during the latter month
the eggs are deposited on the flowers of
the lady’s fingers (Anthyllis vulneraria).

The caterpillars are hatched in about a
week, and commence feeding on the calyx of the buds, and soon
burrow into them till they are quite concealed.

The colour of the caterpillar is brownish, with a darker stripe
on the back, and a row of oblique brown streaks on each side.

This species is widely distributed in England, and is plentiful
in most chalky and limestone districts. It is also found in parts of
Scotland and Ireland.

The Large Blue (Lycæna Arion)

The last of our Blues is the largest of the genus, and is, with
the exception of Semiargus, the rarest. It is a very local insect,[Pg 195]
appearing in small numbers, during June and July, in parts of
South Devon, Gloucestershire, Northamptonshire, and a few other
counties.



Fig. 95.—The Large Blue—Under
Side.

The colour of the upper side
is a dark and rich blue, with a
broad dark border on the hind
margins, and a group of black spots
near the centre of the fore wings.
The under side (fig. 95) is of a
pearly grey, without any red spots,
but having a double border of
black spots, and also an irregular
row of black spots in white rings
across the middle of each wing.

The caterpillar feeds on thyme (Thymus Serpyllum), on which
plant the eggs are laid singly, generally on the flower heads.[Pg 196]


CHAPTER XVI

THE DUKE OF BURGUNDY AND THE SKIPPERS

Family—Erycinidæ

The Duke of Burgundy (Nemeobius Lucina)

The family Erycinidæ has only one British representative, commonly
known as the Duke of Burgundy Fritillary, but although
this butterfly certainly resembles the Fritillaries in general appearance
(see figs. 9 and 10 of Plate VII), its habits and life history
present many points of difference from these.

The upper side is chequered with black and tawny brown, the
fringe is white and barred with dark brown, and a row of tawny
spots with black centres border the hind margins. The under side
has two rows of white spots, one near the base, and the other across
the centre of each wing.

The male has only four legs adapted for walking, but the female
has six.

The butterfly is out in May and June, and frequents the paths
and open spaces of woods, chiefly in the south of England, but it
has been taken in some of the northern counties.

The caterpillar (Plate VIII, fig. 6) is not spiny like those of the
true Fritillaries, but more closely resembles those of the Blues,
being somewhat of the form of a woodlouse. It is reddish brown,
with tufts of hair, black spiracles, and a dark line down the back.
It feeds on the primrose (Primula acaulis) and the cowslip
(P. veris), and may be found during June, July and August.

When fully grown, the caterpillar secures itself to a leaf or stem
by means of its anal claspers and a silken cord round its body, and
changes to a short, thick, hairy and light-coloured chrysalis (Plate
VIII
, fig. 11), which is marked with several black spots. In this state
it spends the winter, and emerges early in the following summer.[Pg 197]

Family—Hesperiidæ—The Skippers

This family contains eight small species, none of which are
remarkable for brilliancy of color. They are, nevertheless, very
interesting creatures, for they exhibit peculiarities of structure and
habit that render them singular among the butterflies, and seem to
show a sort of cousin relationship with the moths. They have
thick bodies that remind us somewhat of the Noctuæ. Their heads
are broad, so that the antennæ, which are slightly hooked at the
tips, are rather wide apart at the bases. When at rest, they
neither press their wings together over their back like the other
butterflies, nor do they set them horizontally after the manner of
the moths, but seem to lay claim to an intermediate position in the
scale of Lepidopterous insects by holding them in a half elevated
position. Their flight, too, is not graceful like that of most other
butterflies, nor even so steady as that of the little flitting blues, but
brisk and erratic, and resembling the fitful motions of moths disturbed
from their slumberings at unwonted hours. Thus they have
earned their popular title of skippers from their habit of skipping
rather than flying from flower to flower. All the three pairs of legs
of these butterflies are fully developed for walking.

The caterpillars have rather large heads, and their bodies taper
from the middle toward both extremities. Like the larvæ of many
moths, they hide themselves in leaves which they have rolled and
secured with silken threads; and when about to change to the
chrysalis state, they also spin silken cocoons for their further
protection.

The Grizzled Skipper (Syrichthus Malvæ)

The ground color of this species is a very dark brown, relieved
by a number of square white spots arranged as shown in fig. 11
of Plate VII. The fringe is wide, and barred with the same two
colours, arranged alternately. The pattern of the under side is
similar, but the dark brown of the upper surface is replaced by a
lighter olive tint.

The butterfly may be looked for in May in the open spaces of
woods, particularly in damp places. It is common all over England,
and is found also in the south of Scotland.

The caterpillar is either green or brownish, with a darker dorsal
stripe of the same color, and two white lines on each side. It
feeds on the raspberry (Rubus idæus), the bramble (R. fruticosus),[Pg 198]
and the strawberry-leaved cinquefoil (Potentilla Fragariastrum),
and is full fed about the end of June.

The chrysalis is greyish, spotted with black. It is rather elongated,
and without angles, but has a short and sharp projection
extending backwards from the ‘tail.’

The Dingy Skipper (Nisoniades Tages)

Colour—a dingy brown, indistinctly barred and spotted with a
darker tint, and having a row of small white spots just inside the
fringe of the hind margins. Under side—a paler brown, with rows
of small white spots.

This butterfly is common in all parts of England, and is found
in a few localities in Scotland and Ireland. It frequents dry
banks, and is particularly partial to the chalky districts of the
south-eastern counties. It is on the wing in May, and a second
brood appears in lesser numbers in August.

The caterpillar is pale green, with two yellow stripes on each
side, and a row of black spots above each stripe. It feeds on the
bird’s-foot trefoil (Lotus corniculatus), and may be found in June,
and again in September.

The chrysalis (Plate VIII, fig. 12) is shaped something like that
of the last species, and is coloured green on the front segments,
and a rose red on the abdomen.

The perfect insect is represented in fig. 12 of Plate VII.

The Small Skipper (Hesperia Thaumas)

In briefly describing the various British butterflies no mention
has been made, except in a few cases, of the shape of the wings,
this matter having been left to the reader’s own observations of
our illustrations. We will, however, call attention to the somewhat
square-cut form of the wings of Thaumas and the following
species.

The above-named butterfly (Plate VII, fig. 13) is a lively-looking
little insect, its wings being of a bright tawny orange
colour, bordered with black, beyond which is a light fringe. The
male, which is the sex figured, is distinguished from the female by
an oblique black streak across the middle of the front wings.
The under side is orange, with a decidedly greenish tinge.

The butterfly is out in July, and is very abundant and widely
distributed. It lays its eggs on various grasses, particularly the
meadow soft-grass (Holcus lanatus).[Pg 199]

The caterpillar hybernates through the winter, and is full fed
in the following June, when it changes to a green chrysalis after
spinning a light silken cocoon among the blades of grass. The
colour of the caterpillar is green, with six longitudinal white
stripes—two on the back, and two on each side.

The New Small Skipper (Hesperia Lineola)

A few years since (1888) a butterfly was taken in one of our
south-eastern counties that closely resembled the well-known
Thaumas (or Linea), but which turned out to be a species not previously
known in Britain. When, however, the distinguishing features
of the new butterfly were made known, several entomologists
discovered that they had already secured the new prize, but that,
being ignorant of its characteristics, they had placed it in their
series over the label Thaumas.

Since the above date, this new insect (Plate VII, fig. 18),
which is named Lineola, has been taken in considerable numbers
at Leigh, Harwich, Southend, and near Shoeburyness in Suffolk,
as well as in the Fens of Huntingdonshire; and it is highly probable
that it may turn up in various other localities where it has
not yet been observed.

It appears on the wing about the first week of July, a little
later than Thaumas, but the two kindred species are often found
flying together.

The chief points by which we distinguish Lineola from the last
species are these: The general appearance of the wings is a bit
dingier than in Thaumas; the inner portion of the hind wings is
of a bright tawny colour in Thaumas but not in Lineola; the tips
of the antennæ are yellow beneath in Thaumas, but black in
Lineola; and the black streak across the fore wings of the latter
species is short and generally broken.

The eggs of Lineola are laid at the end of July or beginning of
August on various grasses, chiefly the various species of Triticum,
but do not hatch till the following April.

The larva is full fed about the end of June or beginning of July,
and then changes to a long yellowish-green chrysalis, from which
the perfect insect emerges in two or three weeks.

The Lulworth Skipper (Hesperia Actæon)

Although this species is somewhat similar to the two preceding,
it may be readily distinguished by the heavy clouding of dull[Pg 200]
greenish brown that almost covers the wings. The male, which is
shown in fig. 14 of Plate VII, has a black streak across the fore
wings, and the female possesses a semicircular row of tawny
spots near the tip of the same wings, and also a tawny streak near
the centre.

This is a very local species, having been found only in a few
localities. At Lulworth Cove and ‘Burning Cliff’ in Dorset it has
been met with in profusion. In Devon it frequents the rough
ground near the cliffs at Sidmouth and Torquay; and it has also
been reported as appearing at Stratford-on-Avon, Shenstone near
Lichfield, and the neighbourhoods of Swanage and Tyneham.

One can scarcely hope to see this insect at large without making
a special trip to one of its favourite haunts, in which case a day
should be chosen toward the end of July or early in August.

The Large Skipper (Hesperia Sylvanus)

During May, June, and August this butterfly may be seen on
grassy banks in nearly every part of England, as well as in certain
localities of Scotland and Ireland.

The wings are all of a bright orange-brown colour, with a narrow
black border, inside which is a broad shading of brown. The latter
colour usually completely covers the hind wings with the exception
of about half a dozen squarish spots; and the same colour, together
with the dark brown wing rays, breaks up the light ground of the
fore wings, often forming several squarish and triangular patches,
most distinct near the tips. The male (Plate VII, fig. 15) may be
readily distinguished from the female by the presence of a thick
dark brown streak across the fore wings.

The under side of both sexes is pale tawny brown, with a
greenish tinge; and has several rather indistinct yellowish spots.

The larva is of a dull green colour, with a dark line on the back.
Its upper surface is dotted with black, and there are white spots on
the under side of the tenth and eleventh segments. It feeds on
several kinds of grasses, some of its favourites being the meadow
soft grass (Holcus lanatus), the cock’s-foot (Dactylis glomerata),
and couch grass (Agropyron repens).

The Silver-spotted Skipper (Hesperia Comma)



Fig. 96.—The Silver-spotted
Skipper—Under
Side.

This species is very similar on the upper side to the last, except
that the squarish spots of both fore and hind wings are much paler[Pg 201]
and much more distinct; and here, too, the male (Plate VII, fig. 16)
is to be distinguished from the female by a black streak crossing
the front wings obliquely. The under surface has a greenish tinge,
more particularly on the hind wings;
and this side is conspicuously marked
with a number of white square spots
with sharp outlines, arranged as shown
in fig. 96.

Although common in some localities,
this butterfly is not widely distributed.
It is confined to some of the
southern and midland counties of England,
and is particularly partial to the
chalk districts of the south-east. On the chalk downs of Kent,
Surrey, and Sussex it is moderately common. It is on the wing
during July and August.

The caterpillar feeds on certain leguminous plants, among which
are the bird’s-foot (Ornithopus perpusillus) and the bird’s-foot
trefoil (Lotus corniculatus).

The Chequered Skipper (Carterocephalus Palæmon)

This is another local insect, more so even than the last, but
it sometimes appears in profusion in certain limited districts.
Kettering, Oundle in Northamptonshire, and Monk’s Wood in
Huntingdonshire are places where it has been taken freely. It
appears in June.

The wings are chequered with very dark brown and orange.
The fore wings are bordered with small rounded yellow spots, and
beside these there are about nine very conspicuous yellow spots on
the fore wing and three on the hind wing. The arrangement of
these markings may be seen in fig. 17 of Plate VII.

The caterpillar feeds on the greater plantain (Plantago major).[Pg 203]


PART IV

COMMON BRITISH MOTHS


CHAPTER XVII

SPHINGES

We have already observed the chief features by which we are able
to distinguish between butterflies and moths (page 56), so we shall
devote the present division to a description of the characteristics
and life histories of some of the latter insects.

The number of British butterflies is so limited that space could
be found for a brief description of every species, but with moths
the case is very different. There are about two thousand known
British species of this division of the Lepidoptera, and every year
adds some newly discovered insects to this long list; we shall
therefore have to content ourselves with making a selection of these
for individual mention.

In doing this I shall endeavour to provide the young entomologist
with a fairly representative list—one that will enable him to
become more or less intimately acquainted with all the principal
divisions of the Heterocera; and his attention will be drawn
especially to many which may be described as ‘common’ or
‘generally distributed,’ so that during his first few seasons at
collecting he may be enabled to identify and study a fair
proportion of his captures. Occasionally, however, one of the
rarer species will be described in order to illustrate some striking
characteristic.

We shall commence with the tribe of Sphinges or Hawk
Moths
.[Pg 204]

This group consists of three families—the Sphingidæ, including
the largest of the ‘Hawks,’ and the ‘Bee Hawks,’ the Sesiidæ or
‘Clearwings,’ and the Zygænidæ, including the ‘Foresters’ and the
‘Burnets’—numbering in all about forty species.

Family—Sphingidæ

This family is named from a fancied resemblance of the larvæ
to the celebrated Egyptian sphinx. The perfect insects have very
thick bodies, generally tapering toward the tail, and their wings are
rather narrow in proportion to the length, but are exceedingly
powerful, and the flight is, with one or two exceptions, very rapid.
The antennæ terminate in a small and thin hook.

Most of these insects fly at dusk, but a few delight in the brightness
and heat of the midday sun. In either case the velocity of
their flight is generally so great that it is a difficult matter to
follow them with the eye, and a still more difficult matter to secure
the insects in the net; consequently, the best way to study them is
to search out the larvæ on their food plants, and rear them till they
attain their perfect form.

The larvæ of the Sphingidæ are large and smooth, and most of
them have a horn projecting from the top of the last segment but
one. They all undergo their metamorphoses under the surface of
the ground.

The Death’s-Head Hawk (Acherontia Atropos)

Our first example of the Sphinges is the beautiful Death’s-Head
Hawk Moth—an insect that often attains a breadth of five inches
from tip to tip when the wings are fully expanded. Its popular
title has been applied on account of the peculiar markings of the
thorax, which are said to resemble a human skull; and this feature
has certainly some connection with the superstitious beliefs of
ignorant country folk concerning this moth. But this characteristic
is probably not the only one that has caused the creature to
be regarded with superstitious alarm. Both its superior dimensions
and nocturnal habits serve to intensify the unfounded fear; but,
what is particularly striking and unique about it is its power of
uttering a squeaking sound, which it does when disturbed. Even
the earlier stages of the insect possess this strange power. The
caterpillar makes a peculiar snapping noise when irritated, and the[Pg 205]
chrysalis has been observed to squeak shortly before the emergence
of the perfect form.

The fore wings of this moth are of a very rich dark brown,
beautifully mottled with lighter tawny shades, and with a small
but conspicuous yellow dot near the centre. The hind wings are
yellow, with a black band and margin; and the body is yellow,
with six broad black bands, and six large blue spots down the
middle.



Fig. 97.—The Death’s-Head Hawk Moth.

The moth is rather widely distributed, and even common in
some parts, but is not nearly so often met with as the larva. It is
on the wing during August and September.

It is probable that the reader will never have an opportunity of
capturing the perfect form of this remarkable species, but he may
with a little perseverance obtain some caterpillars and rear them.
These larvæ feed on the potato, the deadly nightshade (Atropa
Belladonna
), and the woody nightshade (Solanum Dulcamara);
and they are well known to potato growers in some parts of the
country.

The colour of the caterpillar is generally pale yellow, with
numerous small black dots, and seven oblique violet stripes on each[Pg 206]
side. The horn is yellowish and rough, and is bent downward, but
recurved again at the tip.

It feeds during the night, and remains hidden throughout the
daytime. In August it is fully grown, and then retires into the
ground to undergo its transformations.


Fig. 98.—The Larva of Atropos.

The Privet Hawk (Sphinx Ligustri)

This is another fine moth, measuring nearly four and a half
inches from tip to tip. It is represented in the centre of Plate IX
in its natural colours, so that it need not be described.

The perfect insect flies in June and July, and, although common,
is not frequently seen at large. The larvæ, however, are to be met
with in abundance in privet hedges. Even in the centres of large
towns we may see them resting on the topmost twigs of a privet
hedge, their beautiful green tint closely resembling that of the
surrounding leaves. After a little experience they may be readily
discerned by a careful observer, but there are certain signs by which
their presence may be proved before they have been actually
seen. Sometimes a number of the twigs are completely stripped
of their leaves, even the midribs and the leaf stalks being almost[Pg 207]
or entirely devoured; and beneath the bushes are the large black
masses of excrement that tell of the marauders above. When
found, these larvæ should always be removed on a piece of the
twig to which they are attached, for they hold on so firmly by
their claspers that it is sometimes almost impossible to remove
them from their hold without injury.

These caterpillars may easily be distinguished from those of
the other ‘hawks’ by the seven oblique stripes which adorn the
sides. These are each composed of two colours, white and lilac,
and form a pretty contrast with the bright green of the rest of the
body. The horn is smooth and curved, and is black with the
exception of part of the under side, which is yellow.

They are fully grown in August, and from the end of this month
till the following June the chrysalides may be dug out from under
privet and lilac bushes, both of which are attacked by the larva.

The Spurge Hawk (Deilephila Euphorbiæ)

This is a very rare British species; in fact, it has never been
seen in this country in its perfect state, but the larva has been found
plentifully at Appledore and
Braunton Burrows, in North
Devon, feeding on the sea
spurge (Euphorbia Paralias).

The perfect insect is shown
on Plate IX (fig. 2).


Fig. 99.—The Caterpillar of
Euphorbiæ.

The caterpillar is black,
with a large number of small
yellowish white dots, and two rows of spots of the same colour on
each side. There is also a red line on each side, and another down
the middle of the back. The horn is rough and red with a black
tip. It feeds during August and September.

The Small Elephant Hawk (Chærocampa Porcellus)

This pretty insect is one of the smallest of our hawk moths.
It is widely distributed, being met with in many parts of England
and in the south of Scotland. It flies in June.


Fig. 100.—The Small Elephant
Hawk Moth.

The fore wings are of a dull yellow colour, with rosy-red
hind margins, and a broad border of the same tint on the costal
margin. The hind wings have also a rosy-red hind margin,[Pg 208]
and are smoky black along the costæ, and yellow in the anal
angle. The body is coloured with bright rose-red, tinged with
olive on the foremost and hindmost segments.

The popular name of this
and the following species has
been applied because of the
power which the caterpillar
has of extending and retracting
its front segments, a peculiarity
which has given the
idea of a semblance to the
elephant’s proboscis. The
colour of the caterpillar is
light-brown or green, mottled
with dark-brown, dark-green, or black. It has a conspicuous eye-like
spot on each side of the fifth and sixth segments, and has no
horn.

This larva may be found in July and August, feeding on species
of bedstraw (Galium verum, G. Mollugo, and G. palustre), willow
herb (Epilobium hirsutum), or the purple loosestrife (Lythrum
Salicaria
).

The Large Elephant (Chærocampa Elpenor)

This species (Plate IX, fig. 3) is very similar to the last in
form and markings; but is, as its name implies, larger.

The caterpillar, too, is very like that of the last species, but may
be distinguished from it by the possession of a short black horn,
tipped with white, on the ‘tail.’ Its colour is green or brown,
mottled and spotted with black. The eye-like spots on its fifth
and sixth segments are black, and each contains a brown spot
surrounded by a white line.

Its chief food plants are the hairy willow herb (Epilobium
hirsutum
), three species of bedstraw (Galium verum, G. Mollugo
and G. palustre), the purple loosestrife (Lythrum Salicaria),
and the enchanter’s nightshade (Circæa lutetiana). It will also
feed on the vine and the apple in confinement.

The Eyed Hawk (Smerinthus Ocellatus)

Our next genus (Smerinthus) contains three well-known moths,
all of which have the hind margin of the fore wings angulated or
indented.[Pg 209]

The first is the Eyed Hawk, represented in fig. 4 of Plate IX
and named after the beautiful and conspicuous eye-like spot near
the anal angle of each hind wing.

The caterpillar has a rough green skin, sprinkled with white
dots, and marked with seven oblique white lines on each side, each
of which is bordered with dark green above. The spiracles are
pinkish, surrounded by violet rings; and the horn is blue.

The moth flies during May, June, and July; and the caterpillar
may be found in plenty during August, feeding on the apple, willow
(Salix alba), sallow (S. cinerea and S. Caprea), poplar (Populus alba
and P. nigra), aspen (P. tremula), and the blackthorn (Prunus
spinosa
).

As with many other Sphinges, the larvæ are much more commonly
seen than the perfect insects; but the latter may often be
met with resting on tree trunks and fences in the neighbourhood of
their food plants.

The Poplar Hawk (Smerinthus Populi)


Fig. 101.—The Poplar Hawk.

This moth is very common and very widely distributed, and may
be easily found in any of its stages. The perfect insect flies during
May, June, and July; and being rather heavy on the wing, it is easily
taken with a net as it hovers round the branches of its favourite
trees or among the flowers of gardens at dusk. The larva may be
beaten from the boughs of poplars and sallows during August and
September, and during the latter month may often be seen creeping
down and around the trunks of these trees, searching for a suitable
spot in which to undergo its changes. The pupa may be dug out[Pg 210]
of the soil at the foot of the same trees during the autumn, winter,
and spring months.

The fore wings are ashy grey or greyish brown, marbled with
darker tints, with a conspicuous white spot near the centre. The
hind wings are similarly coloured except at the base, where there is
a large patch of brick-red.

The caterpillar is rough, of a pale green colour dotted with yellow,
with seven oblique yellow stripes on each side. The spiracles
are white, edged with red; and the horn is yellow on the upper,
and reddish on the under side. Its chief food plants are the
poplar, the Lombardy poplar (Populus pyramidalis), aspen
(P. tremula), and sallow (Salix Caprea and S. cinerea).

The Lime Hawk (Smerinthus Tiliæ)

This beautiful moth (fig. 5, Plate IX) is easily identified by its
rich olive green and brown wings, the fore pair of which have very
conspicuous patches of deep olive, sometimes uniting to form a
continuous central bar. It flies in May and June.

The caterpillar is rough, of a pale green colour, dotted with yellow,
with seven oblique yellow stripes on each side. Thus it is very
like the larva of Populi, but may be distinguished from that species
by the orange spiracles, and by the horn, which is rough, blue above,
and yellow beneath. Behind the horn, too, there is a flat purple or
violet scale with an edging of orange.

The food plants of this species are the lime (Tilia vulgaris),
elm (Ulmus campestris), and the hazel (Corylus Avellana), from
which the larvæ may be beaten in August and September, and
from under these the pupæ may be dug out during the winter
months.

The Humming-Bird Hawk (Macroglossa Stellatarum)

The genus to which this insect belongs contains three interesting
British species. Their antennæ are thickened toward the end,
but terminate in a small curved bristle. Their wings are rather
short and broad; their bodies are very thick, terminating in a broad
tuft of hair; and the perfect insects fly during the daytime,
delighting in the hottest sunshine. The larvæ feed principally on
low-growing plants, and undergo their metamorphoses on the ground
among the foliage.

On Plate IX (fig. 6) one of these pretty moths is shown. It is[Pg 211]
the Humming-bird Hawk, so called on account of its exceedingly
rapid humming-bird-like flight, accompanied by a soft humming
sound.

This insect is very common; and, being very partial to the attractions
offered by many of our favourite garden flowers, it ought to
be well known to all observers of nature.

Take your stand near a bed of petunias or verbenas, or close to
a honeysuckle in bloom, on any hot summer’s day, and you are
almost sure to be rewarded by a peep at the wonderful flight and
interesting ways of this moth. It makes its appearance so suddenly
that you first view it as an apparently motionless insect, suspended
in the air, and thrusting its long proboscis into the tube of an attractive
flower. Its wings vibrate so rapidly that they are quite
invisible, and give rise to the soft hum already mentioned. Then
it darts from one flower to another, making a similar brief stay
before each while it sucks the grateful sweets. Raise your hand as
if to strike, and suddenly it vanishes you know not where. But it
is as bold as it is wary, and will often return to the selfsame flower
as if to defy your power. A sharp sweep of your net in a horizontal
direction, or a sudden downward stroke, may secure it; but if you
miss it, as you probably will, it will disappear like a phantom, and
give you no opportunity of making a second attempt.

This moth is on the wing throughout the hottest months of the
year—May to September, and will often greet you as you roam over
flowery banks in search of butterflies.

The caterpillar feeds on the lady’s bedstraw (Galium verum),
hedge bedstraw (G. Mollugo), and the goose grass (G. Aparine),
and may be searched for in August and September. It is rough,
green or brownish, and dotted with white. Along each side are two
light lines. The horn is thin and short, rough, and points upwards.

The Broad-bordered Bee Hawk (Macroglossa Fuciformis)

The two other moths of this genus are called Bee Hawks from
their resemblance to the humble bee. They are very much alike,
but may be distinguished by a difference in the width of the dark
border of the wings; and are named Broad-bordered and Narrow-bordered
respectively.



Fig. 102.—The Broad-bordered
Bee Hawk.

The former is illustrated in the woodcut appended. The fore
wings are transparent like those of bees, with a dark central spot
and a broad reddish-brown hind margin. The base and costa are[Pg 212]
black and tinged with green. The hind wings are similarly
coloured, but have no central spot. The body is olive-brown, with
a broad reddish belt, and behind
are tufts of hair, which are
spread out when the insect flies,
just after the manner of the tail
feathers of a bird. The moth
flies in May.

The larva resembles that of
Stellatarum, but exhibits a
violet tint above the legs. Its
horn, too, is curved, and of a
reddish or brownish colour. It
feeds on the honeysuckle (Lonicera
Periclymenum
), ragged
robin (Lychnis Flos-cuculi), evening campion (L. vespertina), red
campion (L. diurna), lady’s bedstraw (Galium verum), and the
field scabious (Scabiosa arvensis), during the month of July.

Family Sesiidæ—The Clearwings

This family contains fourteen very pretty British insects that
differ very much from other moths in many important and interesting
particulars.

Their antennæ, like those of the Sphingidæ, are thickest
beyond the middle, and those of the males are slightly ciliated or
hairy. Their bodies are slender, and terminate behind in tufts of
hair. The hind wings in all cases are transparent, margined and
veined with black or brown; and the fore wings also, in most
cases, have transparent bases.

These moths delight in the hottest sunshine, and may be seen
gracefully hovering over the flowers in our gardens, looking more
like gnats, bees, and wasps, than moths.

The larvæ of these insects are all wood-eaters, and spend their
time within the stems of shrubs and trees, eating out galleries in
the material that forms both their food and their home. Within
these they also undergo their changes, and do not expose themselves
to the free air and light till they reach their perfect
stage.[Pg 213]

The Hornet Clearwing of the Poplar (Trochilium Apiformis)

We can find space for a mention of only two of the clearwings,
the first of which is an insect that closely resembles the dreaded
hornet, and whose larva feeds in the stems of poplars—features
which will account for the above name.


Fig. 103.—The Hornet Clearwing
of the Poplar.

The head of this species is
yellow, its thorax brown with a
large yellow patch on each side,
its abdomen yellow with two
brown belts, and its legs reddish
orange. The front wings are
transparent, with brown costæ,
and all the wings are margined
with brown.

The caterpillar, when full
fed, makes a cocoon with silk
and the chips of wood that it
has bitten off; and in this undergoes
its metamorphoses. It is fully grown in April, and the moth
flies from the end of May to the end of July.

There is another ‘Hornet Clearwing,’ the larva of which feeds
on the stems of osiers. It may be distinguished from the species
just described by a yellow ‘collar’ between the head and thorax,
both of which are blackish.

The Currant Clearwing (Sesia Tipuliformis)


Fig. 104.—The
Currant
Clearwing.

This is by far the commonest of all the Clearwings, and only too
well known to those who grow currants. Examine the shoots of
Ribes rubrum (red currant) and R. nigrum (black
currant), especially those that present a withered
or half-withered appearance, and you will almost
certainly meet with signs of the presence of this
intruder. Little wriggling larvæ occupy the pithless
stems throughout the winter and spring.
These are full grown in April, and in June the
pretty little moth emerges through a hole in
the side of a shoot, leaving the empty pupa case
within its former home.

The fore wings of this moth have black margins, and a black
transverse bar beyond the middle. The body is black, with three
pale yellow belts, and black tufts of hair at the tip.[Pg 214]

Family—Zygænidæ

The remaining family of the Sphinges—the Zygænidæ—includes
seven British species, three of which are known popularly as the
Foresters and the others as the Burnets.

Their antennæ are thickest beyond the middle, but do not
terminate in a hook. Their wings are narrow and completely
covered with scales.

These moths are very sluggish creatures, spending the greater
part of their time at rest on the stems of low-growing plants. When
they do fly, their flight is short and heavy, and their pretty wings
glisten in the sunshine (for they are lovers of the sun), giving them
the appearance of bees rather than of moths. On account of this
natural sluggishness, they are exceedingly local, for they never
move far from the spots where their food plants abound, and where
they had previously spent the earlier stages of their existence.
Thus we often come across a very limited piece of ground actually
alive with them, and outside which not a single specimen is to
be seen.

The larvæ, too, are sluggish creatures, with soft and plump
cylindrical bodies and no horns. I will briefly describe three
members of this family.

The Forester (Ino Statices)


Fig. 105.—The
Forester.

The fore wings of this species are semi-transparent, and of a
beautiful glossy green. The hind wings also are semi-transparent,
but of a dull smoky tint. The thorax and abdomen are both of a
brilliant metallic green colour. The tips of the
antennæ are blunt, and the male may be distinguished
from his mate by these organs being
slightly fringed or ciliated.

The caterpillar is dingy grey or greenish,
with a row of black spots down the back, and
a whitish stripe on each side. It feeds on the
common sorrel (Rumex acetosa) and the sheep
sorrel (R. acetosella), and when fully grown it spins a cocoon on
the stem of its food plant, and there changes to a chrysalis.

The larva may be found during May and early June. The
chrysalis state lasts only a few days, and the moth is on the wing
during June and July.[Pg 215]

The Broad-bordered Five-spotted Burnet (Zygæna Trifolii)

On Plate IX (fig. 7) will be found a coloured representation of
this Burnet. The two crimson spots in the base of the fore wing
are very close together, and often touch. The same remark also
applies to the two spots on the middle of the wing. A glance at
the list of British Moths (Appendix I) will show that we have also a
Narrow-bordered Five-spotted Burnet. This insect is very similar
to the species now under consideration, but may be identified by
the narrower purplish margin on the hind wings, and also by the
shape of the antennæ, which are not thickened so much near the
end as they are in Trifolii.

The larva of the present species is yellowish or greenish, with a
row of black spots on the back and a row on each side. It feeds on
the bird’s-foot trefoil (Lotus corniculatus), hop trefoil (Trifolium
procumbens
), and the horse-shoe vetch (Hippocrepis comosa) in
May. Late in May or in early June the chrysalis may be found
in a silken cocoon attached to a stem or leaf; and the perfect
insect flies during June and July.

The Six-spotted Burnet (Zygæna Filipendulæ)


Fig. 106.—The Six-spotted
Burnet.

So common is this moth, and so conspicuous when it flies in the
blazing sun, that it must be familiar to almost everybody. On a
bright midsummer day hundreds may often be started from their
grassy beds from one little patch of ground.

The colouring of the wings is much the same as in the last
species, but there are two crimson spots instead of one near the
tips of the fore pair.


Fig. 107.—The Larva of
Filipendulæ.

The larvæ may be seen in vast numbers during May and June,
feeding on clovers (Trifolium pratense and T. repens), and the[Pg 216]
bird’s-foot trefoil (Lotus corniculatus); and in the latter month
thousands of the chrysalides, inclosed in shuttle-shaped cocoons on
grass stems, may be seen on downs and sunny banks in almost
every part of the country.

The caterpillar, which is yellow, may be known by the two
rows of black spots that adorn each segment of the body.[Pg 217]


CHAPTER XVIII

BOMBYCES

This tribe is an important one, inasmuch as it contains those few
moths whose silk is of present or anticipated commercial value.
Many of the British members, even, make silken cocoons of moderate
compactness, but none of them yield a quantity and quality of
silk to justify any attempt to utilise it in the arts.

There are more than a hundred British species in this group,
and these represent no less than seventeen families, which exhibit a
great variety in their general appearance and habits.

Family—Nycteolidæ

The Green Silver-lined (Hylophila prasinana)

This family, under the name of Chloephoridæ, is included by
some authors among the Tortrices (page 298), which they somewhat
resemble in habits. It contains
only four species, of which we will take
one example—the Green Silver-lined.


Fig. 108.—The Green
Silver-lined.

The fore wings of this insect are pale
green, with three oblique silvery white
lines, the middle one of which is far more
distinct than the other two. The hind
wings are silvery white in the female, and
yellow in the male. It flies in May, and
is common in the wooded districts of the
south-eastern counties.

The caterpillar is pale green, dotted and striped with yellow,
and has a reddish transverse band on the second segment. It
feeds on oak (Quercus Robur), birch (Betula alba), hazel (Corylus[Pg 218]
Avellana), beech (Fagus sylvatica), and alder (Alnus glutinosa),
from which trees it may be beaten in July and August.

Family—Nolidæ

The Short-cloaked Moth (Nola cucullatella)

We select this common moth as a representative of the small
family Nolidæ, which contains only five British species. These are
all small insects. They are nocturnal in their habits, and may be
found at rest on the trunks of trees during the daytime. The caterpillars
are hairy, and undergo their metamorphoses
within silken cocoons.


Fig. 109.—The
Short-cloaked
Moth.

The fore wings of Cucullatella are pearly
grey, with a dark patch at the base, a triangular
spot on the middle of the costal margin,
and wavy lines beyond this, parallel with
the hind margin. The hind wings are grey,
and devoid of any markings.

The caterpillar is of a brownish colour, with a line of lighter
patches down the back, and it is covered with little tufts of hair.
It feeds on the blackthorn (Prunus spinosa), whitethorn (Cratægus
oxyacantha
), and also on plum trees in our gardens during the
month of May. The moth is on the wing during June and July.

Family—Lithosiidæ

The Muslin Moth (Nudaria mundana)

The family Lithosiidæ contains several small moths, distinguished
from the other Bombyces by the narrowness of their fore
wings. When the insects are at rest, all the wings are wrapped
closely round the body. They fly at dusk on
summer evenings, but may be obtained during
the daytime by beating the boughs of trees. If
an open net be held under the boughs during
this operation, the moths will generally feign
death and allow themselves to fall into it when
they are disturbed.


Fig. 110.—The
Muslin Moth.

Most of the larvæ of this family feed on the
lichens that cover walls and the bark of trees, and they conceal
themselves so artfully among this peculiar vegetation that it is no
easy matter to search them out; probably many still remain unknown
to entomologists.[Pg 219]

Our first example—the Muslin Moth—has light brownish-grey
and semi transparent wings, the front pair of which have darker
markings arranged as shown in the illustration. It is a common
moth, and may be met with in July and August.

The caterpillar feeds on lichens in June. It is of a dull grey
colour, with a yellow stripe down the back, and has numerous
little tufts of light hair.

The Common Footman (Lithosia lurideola)


Fig. 111.—The Common
Footman.

The fore wings of this species are of a leaden grey, with a
bright yellow costal stripe which dwindles
to a point just before it reaches the
tip. The hind wings are very pale
yellow.

The larva is black, with a reddish
line on each side just above the feet.
It may be found during May and
June among the lichens of oaks, blackthorns,
and firs, especially in the woods
of the south of England.

The perfect insect flies during July and August.

Family—Eucheliidæ

The Cinnabar (Euchelia Jacobææ)

The family Eucheliidæ contains only four British species, two
of which must receive a share of our attention. The first of these
is the Cinnabar Moth, which is
common in all localities where its
food plants—the groundsel (Senecio
vulgaris
) and the ragwort
(S. Jacobæa)—abound.


Fig. 112.—The Larva of
Jacobææ.

Its colours are so striking that
a glance at its representation (fig. 1
of Plate X) will render a written
description quite unnecessary.

The caterpillar is a very familiar and conspicuous object. Its
colour is bright orange, broken by several broad black rings; and
its body is thinly covered with hair. When fully grown (July or[Pg 220]
August) it descends to the ground, and there changes to a smooth
and shining reddish-brown chrysalis.

The moth appears in June or early in July.

The Scarlet Tiger (Callimorpha Dominula)


Fig. 113.—The Scarlet Tiger.

This is certainly one of the most beautiful of all our moths.
Its fore wings are dark olive green, with a lovely metallic lustre,
and boldly marked with large white and yellow spots. These spots
are arranged generally like those in the illustration, but are subject
to great variation. The hind wings are crimson, with large black
patches, chiefly distributed
near the hind margin. The
thorax is black, with two
white streaks; and the abdomen
crimson, with a
black line down the back.

This moth is a common
one. It may be taken in
June and July. I have
seen it flying somewhat
freely while the sun was still shining brightly.

The caterpillar is very dark lead colour, nearly black; and is
covered with little wart-like projections, from each of which protrudes
a short black hair. There is a broad yellow broken line down
the back, and two others on the sides. It feeds on the hound’s-tongue
(Cynoglossum officinale) and many other low-growing
plants, hybernates through the winter, and is fully grown in May.
Like the other members of this family, it spins a light silken
cocoon, in which the hairs from its body are interwoven.

Family—Cheloniidæ

The Wood Tiger (Nemeophila Plantaginis)

The Cheloniidæ are popularly known as the Tigers—a title
suggested by the tiger-like colouring of some of the prominent
species. They differ from the Scarlet Tiger and the other
members of the Eucheliidæ in that the males have ciliated or
fringed antennæ. The larvæ, too, are more densely covered with
hair.

The Wood Tiger (fig. 2, Plate X) is a beautiful insect, somewhat[Pg 221]
variable in its markings, but so conspicuously coloured that
our illustration cannot fail to lead to its identification. It may be
found commonly among the undergrowth of our southern woods
during May and June.

The caterpillar is dark brown or brownish black, covered with
little hair-bearing warts. The hairs are long and black on the foremost
and hind segments, but shorter and of a brown colour on the
middle of the body. It issues from the egg in September, feeds for
a week or two on the leaves of violets (Viola canina and V. odorata),
heartsease (V. tricolor), plantain (Plantago), or groundsel (Senecio
vulgaris
), and then hybernates till the following March. It is
fully grown in May, and then spins a light cocoon, with which its
hairs are interwoven, among the leaves of its food plant.

The Tiger (Arctia caia)

This splendid moth is exceedingly variable in its colour and
markings, but its usual appearance corresponds closely with that of
the illustration on Plate X (fig. 3). In some specimens the cream
colour almost entirely covers the fore wings, while in others all four
of the wings are completely covered with shades of brown. This
insect is probably known to all my readers, for it is abundant everywhere.

The larva is as well known as the perfect insect. It is a kind
of universal feeder, partaking readily of almost every low-growing
plant, with perhaps a special partiality for dead nettles (Lamium
album
and L. purpureum). It feeds also on the lime tree (Tilia
vulgaris
), and is commonly met with on apple trees and on the
various plants of our flower beds. The young caterpillar makes its
appearance in the autumn, and hybernates after feeding for two or
three weeks only. It is full grown in June, when it spins a silken
cocoon, and changes to a shiny black chrysalis.

The ground colour of the larva is black, but it is covered all over
with long hairs, those down the middle of the back being grey, and
the others brown. This familiar larva is known popularly as the
Woolly Bear.

The Cream-spot Tiger (Arctia villica)

There is yet another Tiger—the Cream-spot—too beautiful and
too common to be excluded from our list. It is represented on
Plate X (fig. 4); and, like the others of its genus, is so boldly marked
that mistaken identity is impossible.[Pg 222]

It is a very sluggish moth, more often seen at rest than on the
wing, and will suffer itself to be roughly handled without making
any attempt to escape.

The caterpillar may be observed on sunny banks, generally feeding
on chickweed (Stellaria media) but sometimes on various
other low-growing weeds, including the dock and the dandelion.
Its colour is black, with red head and legs, and its body is covered
with long brown hairs. It commences to feed in the autumn,
hybernates throughout the winter, and is full grown in May,
towards the end of which month it changes to a black chrysalis
within a light silken web.

The perfect insect appears in June.

The Buff Ermine (Spilosoma lubricipeda)

The Cheloniidæ also include three moths that are popularly
known as the Ermines, two of which—the Buff and the White—are
exceedingly common, and are
among the constant visitors to our
gardens during June and July.


Fig. 114.—The Buff Ermine.

The Buff Ermine has all four
wings of a buff or ochreous tint, and
spotted with black as here represented.

The caterpillar is whitish, with
a white line down the middle of the
back, and its body is covered with
long light brown hairs. It feeds on the dock (Rumex) and many
other low-growing plants during August and September, and spends
the winter in the chrysalis
state, lying within a loose
cocoon on the surface of the
ground.

The White Ermine (Spilosoma Menthastri)


Fig. 115.—The White Ermine.

In this species the wings
are of a pale cream colour,
and the dots of the fore wings are more uniformly distributed than
in the last. Its habits and life history closely correspond with[Pg 223]
those of Lubricipeda, and its larva may be found feeding on the
same plants.

This latter may be distinguished from the caterpillar of the last
species by the dark brown or black colour of the body, and the
presence of an orange line down the back. It is covered with long
brown hairs.

Family—Hepialidæ

The five species which compose this family are known as the
Swifts, a title which they have earned by their rather rapid flight.
Their wings are narrow, and the antennæ very short.

In the larval state they are long, naked and unsightly grubs,
that live under the surface of the ground and feed on the roots of
plants. The chrysalides are armed with short spines projecting from
the segments.

The Ghost Swift (Hepialus Humuli)


Fig. 116.—The Ghost Swift—Female.

One of the commonest of these moths is the Ghost Swift, which
may be seen in hundreds on waste places in the south of England
during the month of
June. The wings
of the male are
white, with a silky
gloss, and a very
narrow brown margin.
The fore wings
of the female are
yellow, marked with
irregular reddish
lines. The hind wings are of a dull smoke colour.

The larva is pale yellow, with a brown head, and a brown horny
plate on the front of the second segment. It feeds throughout the
winter on the roots of numerous plants, including the dock, dandelion,
burdock, white dead nettle, black horehound, and the hop.

The Common Swift (Hepialus lupulinus)


Fig. 117.—The Common
Swift.

The fore wings of the male of this species are brown, with a bent
whitish streak, sometimes broken, passing from the base to the
middle of the inner margin, and then to the apex. The hind wings[Pg 224]
are smoke coloured, with a light brownish fringe. The female is
much less distinctly marked, and presents
a rather dingy appearance.

The larva is dingy white, with brown
horny plates on the second, third and fourth
segments. It feeds on the roots of dead
nettles (Lamium album and L. purpureum),
black horehound (Ballota nigra),
and various other herbaceous plants,
throughout the winter months, and is full
grown in April.

This insect is abundant everywhere in waste places, and may be
seen on the wing in May and June.

Family—Cossidæ

The members of this family have longer antennæ than the
Hepialidæ, and the females are provided with extended ovipositors
which enable them to place their eggs in the deep crevices of the
bark of trees.

The larvæ are naked or only very slightly hairy, and have a
plate on the second segment. They feed on the wood of trees or
the interior of the stems of reeds. The pupæ have spiny projections
on each segment.

The Goat Moth (Cossus ligniperda)

There are only three British species of this family, the largest of
which is the Goat Moth, so called on account of the characteristic
odour of the larva, an odour said to resemble that emitted by the
goat.


Fig. 118.—The Goat Moth.

Fig. 119.—The Larva of Ligniperda
(less than half full size).

The fore wings of this fine moth are pale brown, clouded with
white, and marked by numerous wavy transverse lines. The hind
wings are somewhat similar, but of a duller tint, and the markings
are less distinct. Its average breadth from tip to tip is over three
inches, and it sometimes reaches nearly four inches.

The larva is a most interesting creature. It is dark reddish
brown on the back, and flesh colour beneath; and its head is
intensely black. It feeds on the solid wood of the willow, poplar,
oak, elm, and other trees. The infected trees are often so riddled
with the burrows of these larvæ that they are completely destroyed,
[Pg 225]
and the presence of the intruders is frequently indicated by a heap
of small chips of wood lying on the ground near the roots. The
odour of the larvæ, too, is so powerful, that there is generally no
difficulty in ascertaining their whereabouts by it alone.

It is not always in living trees, however, that we find these
creatures, for they often feed on rotting wood, such as the
remains of old palings and
posts, that lie on the ground
in damp places.

When fully grown they
construct a strong cocoon of
chips of wood, bound together
by silk, and within this they
change to the chrysalis.

The moth emerges in June or July, and is commonly found
resting on the bark of willows and poplars during the daytime.

The Leopard Moth (Zeuzera pyrina)


Fig. 120.—The Leopard Moth.

Fig. 121.—The Larva of Pyrina
(only partly grown).

The wings of this species are white and semi-transparent, and
marked with numerous bluish-black spots in such a way as to
remind one of the skin of the leopard. Its body is very long, and[Pg 226]
the antennæ of the male are doubly fringed for about half their
length from the base.

The caterpillar feeds on the wood of various trees—elm, apple,
pear, ash, alder, poplar, horse chestnut, birch, lilac, and several
others. It is yellowish, with
black shiny spots, and a black
plate on the second segment.

The moth appears in July,
and is widely distributed. It
is attracted by bright lights,
but the best way to obtain it is
to search the trunks and branches of trees that are known to
harbour the larvæ early in the morning, and so obtain newly
emerged specimens.

Family—Liparidæ

Passing over the two small species which are the only British
representatives of the family Cochliopodidæ, we come to the
interesting Liparidæ, the remarkable feature of which is that most
of the caterpillars are adorned with brush-like tufts of hair, and
even the chrysalides are hairy.

The perfect insects are not brilliantly coloured, but generally
display very pale tints; and the antennæ of the males are
pectinated or feathered.

The Brown Tail (Porthesia chrysorrhœa)


Fig. 122.—The Brown Tail.

The family contains two moths—the Brown Tail and the Yellow
Tail—that are very similar in appearance and habits. Both have[Pg 227]
white wings, and their bodies also are white with the exception of
the tuft of coloured hair at the tip of the abdomen, which gives the
names to the species. Their larvæ may both be found feeding on
the same trees (whitethorn), and both change to a brown hairy
chrysalis within a loose cocoon among the leaves.

The larva of Chrysorrhœa is black,
with four rows of little wart-like projections
on each side, from which proceed
little tufts of hairs. These hairs
are reddish with the exception of one
row on each side, which is white. The
tenth and eleventh segments have each
a scarlet tubercle, and there are also
other small spots of the same colour on some of the front segments.

The larva feeds on the blackthorn in addition to the tree
mentioned above, and is full grown in June. The moth flies in
August.

The Gipsy (Ocneria dispar)


Fig. 123.—The Gipsy—Male.

The fore wings of the male are smoky brown, with darker
markings, including a V-shaped black mark near the centre. The
hind wings are brown, darker near the margin. The female is
dingy yellowish white, with darker
markings arranged as in the male.
The male is much inferior in size,
and its antennæ are very strongly
pectinated.

The larva is brownish black,
finely dotted with yellowish grey.
There is a grey stripe down the
middle of the back, and six tubercles
on each segment give rise to
tufts of long hair. It feeds on the whitethorn (Cratægus oxyacantha),
blackthorn (Prunus spinosa), and various fruit trees.

The caterpillar is full grown in June, and the moth appears in
August.

The Black Arches (Psilura Monacha)


Fig. 124.—The Black Arches—Male.

The fore wings of the Black Arches are white, marked with
zigzag black lines as shown in our illustration. The hind wings[Pg 228]
are smoky grey. The hinder segments of the abdomen are banded
with black and rose-pink. The male is much smaller than the
female, and has the antennæ
strongly pectinated.

The caterpillar is hairy, and
of a greyish-white colour. A
brown stripe runs down the
back. On the top of the second
segment are two blue tubercles;
and there is also a tubercle, of a
reddish colour, on each of the
ninth, tenth, and eleventh segments.
It feeds on the oak, birch, fir, and the apple; and is full
grown in June or July.

The moth flies during July and August.

The Vapourer Moth (Orgyia antiqua)


Fig. 125.—The Vapourer
Moth—Male.

Fig. 126.—The Female
Vapourer.

During the hottest summer months, and particularly in August
and September, a rather small brown moth may be seen almost
everywhere, flying rapidly and in a very erratic manner in the bright
rays of the midday sun. This is the common Vapourer Moth,
which may be known at once by its bright chestnut colour, with
darker transverse markings, and a white crescent-shaped spot in
the anal angle of the fore wings. It seems somewhat partial to
civilised life, for it frequents the streets of our metropolis, even in
the very densely populated parts; and the larva is one of the
commonest of the insect forms infesting our gardens and squares.

The caterpillar is variously coloured; but the prevailing tints
are dark brown, grey, and pink. On the second segment are two
long tufts of hair directed forward, and on the twelfth segment a
similar tuft directed backward. On each of the segments five to[Pg 229]
eight inclusive is a brush-like tuft of yellowish hairs. It feeds on
almost every tree usually to be found in parks and gardens.


Fig. 127.—Larva of the Vapourer Moth.

When fully grown it spins a web on the bark of a tree, or on
a wall or fence, and
changes to a hairy
chrysalis.

The female of this
species is wingless, and
never moves away
from the cocoon out of
which she has crawled,
but lays her eggs on
the outside of the silken web, and there remains to die.

The clusters of eggs may be found in abundance throughout the
winter months.

Family—Bombycidæ

This family contains eleven thick-bodied moths, mostly of large
size, in which the predominating colours are greys and browns.
Their hind wings are generally paler than the front pair, and less
distinctly marked; and the antennæ of the males are pectinated.

The caterpillars are very hairy, but the hairs are uniformly
distributed, and not arranged in tufts as in the larvæ of the last
family.

The chrysalides are inclosed in silken cocoons, but are not
hairy.

We shall briefly examine three of the members of this family.

The Oak Eggar (Bombyx Quercus)

The male of this species is shown on Plate X (fig. 5). The
female is much larger, and of a pale tawny colour.

The ground colour of the caterpillar is black; but it is so closely
covered with short yellowish brown hairs that the black is scarcely
visible, excepting when the creature rolls itself up into a ring,
which it does when alarmed. The spiracles are white, and there
is a series of white spots down the middle of the back and along each
side. It feeds on whitethorn (Cratægus oxyacantha), heather
(Calluna, Erica), poplar (Populus nigra), and various other plants
and trees.[Pg 230]

As a rule the larva hybernates through the winter, is full grown
in the following May, and the moth appears in July; but in
Scotland the caterpillar does not spin its cocoon till September,
hybernates in the chrysalis state, and emerges in the following
June. The same is true of the Cornish Eggars; but along the
coast of South Devon both varieties are to be met with.

The male Eggar seems to enjoy the bright sunshine, for I have
seen large numbers flying over the rugged cliffs of the south-west
throughout all hours of the day.

The Drinker (Odonestis potatoria)

The popular name of this species is applied on account of a
peculiar feature of the larva, which sucks up the dewdrop that lies
on its food plant.


Fig. 128.—The Drinker—Male.

The colour of the male is tawny and brown, with a reddish tinge;
that of the female is yellow.
The front wing has an oblique
dark bar passing from the apex
to the middle of the inner
margin; also two white spots—one
in the middle of the
wing, and the other between
it and the costal margin.

The caterpillar is dark
bluish grey above, and has a
line of orange spots on each
side. Along the spiracles are
oblique orange streaks, and a series of tufts of white hair. It feeds
on the annual meadow-grass (Poa annua), and several other grasses.
It is a hybernator, commencing its caterpillar state in the autumn,
and reaching its full dimensions about the end of the following May.

The moth flies during July and August.

The Lappet (Lasiocampa quercifolia)

Our last example of the Bombycidæ is the Lappet (Plate X,
fig. 6), a large moth, the female often measuring considerably
over three inches from tip to tip. The wings are of a rich reddish
brown, and exhibit a beautiful purplish bloom in a newly emerged
insect. Scalloped black lines pass transversely across each wing,
and a small black dot lies near the centre of the fore wings.[Pg 231]

The caterpillar is very variable in colour, but is usually grey or
reddish brown. A deep purple band lies between the second and
third segments, and another between the third and fourth. On the
twelfth there is a small hump, and a pale stripe, more or less distinct,
runs along each side. It feeds on the blackthorn (Prunus spinosa),
buckthorn (Rhamnus catharticus), and the white willow (Salix
alba
).

The moth is not uncommon, and is on the wing in June.

Family—Endromidæ

The Kentish Glory (Endromis versicolor)

The beautiful Kentish Glory is the only British representative of
its family. The male is shown in Plate X (fig. 7); the female is
larger and similarly marked, but its colours are not so bright.

This moth is not common, but may be seen occasionally in the
birch woods of the southern counties. The males fly rapidly in the
bright sunshine, but the females must be searched for on the bark
and branches of the trees.

The eggs are laid in April on the twigs of the birch (Betula alba),
and the young caterpillar emerges early in May. It is gregarious
at first, but loses its social tendencies as it gets older. When full
grown, it is of a pale green colour, with white spiracles, a dark green
line down the back, and an oblique white stripe on each side of
each segment. The sides are dotted with black and brown, and
there is a conspicuous hump on the top of the twelfth segment.

When fully grown it spins a cocoon among the dead leaves
beneath the tree, and in this it spends the winter months in the
chrysalis state.

Family—Saturniidæ

The Emperor Moth (Saturnia pavonia)

Here is another family with but one British member; but in this,
as in the last case, the only representative is a really beautiful insect.
The male Pavonia is shown on Plate X (fig. 8), and will
need no written description as an aid to its identification. The
female is larger, and similarly marked, but the ground colour of the
wings is pale grey.

This moth is abundant almost everywhere, and may be looked
for in the neighbourhood of heaths and woods early in the month of
May.[Pg 232]

The larva feeds on a large number of plants and trees, among
which may be mentioned the willow (Salix alba), blackthorn (Prunus
spinosa
), elder (Sambucus nigra), whitethorn (Cratægus oxyacantha),
bramble (Rubus fruticosus), heaths (Erica tetralix and
E. cinerea), and the meadow-sweet (Spiræa ulmaria). Its colour
is a lovely green; and each segment has several pink tubercles, each
surrounded by a black ring, and giving rise to a tuft of short black
hairs. The spiracles are orange.

In the autumn it spins a pear-shaped cocoon of silk, open at the
small end (fig. 28).

It may here be mentioned in passing that, in the case of some
of the larger moths of the few preceding families, the young entomologist
is likely to meet with larvæ more frequently than the perfect
insect. These moths, however, are mostly very hardy and
easily reared; and a beginner cannot do better than endeavour to
obtain either ova or larvæ, in order that he may be able to watch
the different species through their various stages.

Family—Drepanulidæ

We now reach a family containing six small moths that differ
in many important particulars from those we have just been considering.
They are of such slender build that a beginner may
easily mistake them for Geometers. Their wings, though small,
are broad, and well proportioned to their bodies. In five cases out
of the six the front wings are more or less hooked at the tips, and
on this account the moths in question are called the Hook Tips.

The larvæ are not hairy, but they all have little fleshy projections
on their backs. Their bodies also taper to a point behind, and the
last pair of claspers are wanting, so that they have only fourteen
walking appendages. When at rest they usually fix themselves by
their claspers only, their pointed ‘tails’ being directed slightly upward,
and all the front segments being also elevated. When about
to change, they descend to the ground, and spin their cocoons among
dead leaves.

Two only of this family can receive an individual notice.

The Oak Hook Tip (Drepana binaria)

This can hardly be described as a very common moth, but it is
fairly plentiful in the woods of the southern counties of England.[Pg 233]


Fig. 129.—The Oak
Hook Tip.

Its wings are yellowish brown, marked with two lighter transverse
lines. There are two black spots between the lines of the
fore wings. The antennæ of the male are
pectinated; those of the female simple.
The latter sex is further distinguished by
the paler colour of the hind wings.

The larva is brown, with a broad stripe,
edged with yellow, down the back. There
are two projections on the back of the
fourth segment. It feeds on oak (Quercus
Robur
) and birch (Betula alba).

This moth is double-brooded, and may be seen on the wing in
June and August. The larva may be beaten from the above-mentioned
trees in June and July, and again in September.

The Chinese Character (Cilix glaucata)


Fig. 130.—The Chinese
Character.

The fore wings of this species are white, with a broad dark
blotch from the inner margin to near the costa. The central portion
of this blotch is marked with silvery
spots which are said to resemble Chinese
characters. The hind margin is shaded
with a dark grey border, inside which is a
row of dark spots. The hind wings are
clouded with grey.

This moth is widely distributed, and
seems to be common throughout England. It is double brooded, the
first brood appearing in May and June, and the second in August.

The caterpillar, which is brown, with two prominent tubercles
on each of the third and fourth segments, feeds on the whitethorn
(Cratægus oxyacantha), and the blackthorn (Prunus spinosa).

Family—Dicranuridæ

The five British species that represent this family are such
interesting insects that we should like to have given a detailed description
of all of them, but our limited space will allow of no more
than an outline of the general characteristics of the group and a
selection of two for individual mention.

They are thick-bodied moths, and the prevailing colours are
white and shades of grey. The antennæ are pectinated in the males,[Pg 234]
and, with the exception of the Lobster Moth (Fagi), in the females
also.

The larvæ, like those of the last family, have no anal claspers,
and stand, when at rest, with both ends of the body raised. They
have two ‘tails’ projecting from the last segment. The largest of
them (the Puss), and three smaller species (Kittens) that closely
resemble it in habits, all construct hard cocoons to be presently described;
but the larva of the Lobster Moth spins a light cocoon
among the leaves of trees.

They all spend the winter in the chrysalis state.

The Poplar Kitten (Dicranura bifida)


Fig. 131.—The Poplar Kitten.

Our illustration shows the arrangement of the white and grey on
the wings of this moth, but the other Kittens (Bicuspis and Furcula)
so closely resemble it that it is necessary to point out a mark of distinction.
It will be observed that the fore wings are crossed by a
broad grey band, edged with black. This band, in the present
species, is almost of the same width throughout, its interior margin
being almost straight, and the exterior one slightly concave. In
Furcula, the outer margin of the
band is generally sharply bent inward
just below the costa. In Bicuspis
the grey band varies considerably
in shape, but both this and the
dark blotch near the tip of the wing
are more sharply defined than in
the other two species.

The caterpillar is green, dotted
with brown, and has a brown stripe on the back. This stripe is
broken on the third segment, and widens out on the eighth and
thirteenth segments. It feeds on the Poplar (Populus nigra) and
Aspen (P. tremula).

When full grown it descends to the trunk of the tree, and constructs
a very hard cocoon of a glutinous substance from its own body
mingled with little pieces of the bark that it removes for the
purpose. Thus made, the cocoon so closely resembles the surrounding
bark that detection is very difficult. I have frequently
found these cocoons on the inner surface of loose bark.

This moth is widely distributed, and may be searched for in
June and July. The larva feeds during August and September.[Pg 235]

The Puss (Dicranura vinula)


Fig. 132.—The Puss Moth.

No written description is necessary in this case, the illustration
easily serving for identification. This beautiful moth flies in May
and June, and is common everywhere.

The caterpillar is a very interesting creature. It is green, with
a hump on the fourth
segment, and a patch
of brown from the
fourth segment to the
tail. This patch is
very wide on the
eighth segment, but
tapers to a point on
the thirteenth. The
two horns are rather
long and rough, and
from each of them a
very slender pink filament
is protruded when the caterpillar is irritated.

It constructs a cocoon very similar to that of Bifida, though of
course larger, on the bark of the tree on which it fed, generally
three or four feet from the ground. It feeds on sallows, willows,
and poplars, and may be found during July and August.

Family—Notodontidæ

The Coxcomb Prominent (Lophopteryx camelina)

The family Notodontidæ contains several moths of somewhat
varied appearance, but foremost among them are the ‘Prominents,’
distinguished by a conspicuous projection
on the inner margin of the
fore wings.


Fig. 133.—The Coxcomb
Prominent.

Our example of this group is the
Coxcomb Prominent.

Its fore wings are brown, with
darker markings arranged as shown
in the illustration; and the hind
margins are scalloped. The hind
wings are much paler, with a dark brown patch in the anal angle.

The caterpillar is green, with a yellowish line on each side.
The spiracles are black, and there are two small humps on the[Pg 236]
twelfth segment. It feeds during August, September, and October,
on various trees, including the oak, birch, poplar, hazel, and
alder.

The moth flies from June to August, and is moderately common
and widely distributed.

Family—Pygæridæ

The Buff Tip (Phalera bucephala)

The first of our two examples of this small family is the common
and destructive Buff Tip. The perfect insect is represented on
Plate X, fig. 9, and is too well known to require a lengthy description.
During June and July it may be seen resting on the bark of trees
almost everywhere, with its wings folded closely round its body,
and its antennæ tucked under the wings, looking just like a piece of
stick, or a projection of the bark on which it sits.


Fig. 134.—The Larva of Bucephala.

The caterpillars appear towards the end of June, and may be
seen in dense clusters on lime and other trees, sometimes twenty
or thirty huddled together on a single leaf. As they grow larger
they retain their gregarious tendencies, and often completely strip
the leaves from large branches. They are of a dull yellow colour,
hairy, and have seven broken black lines, one along the middle of
the back, and three on each side. The head and legs are black.

When full grown, they descend to the root of the tree, burrow
into the soil, and there remain in the chrysalis state till the following
June. The chief food plants of this species are the lime (Tilia
vulgaris
), elm (Ulmus campestris), and hazel (Corylus Avellana).[Pg 237]

The Chocolate Tip (Pygæra curtula)

This species is not nearly so common as the last, but is to be
met with more or less in most of the English counties in the month
of May.


Fig. 135.—The Chocolate
Tip.

Its fore wings are light greyish brown, crossed with four transverse
paler streaks, and tipped with a patch of chocolate brown.
The hind wings are pale yellowish
grey.

The young caterpillars feed in companies
between leaves which they have
spun together, but when nearly full
grown they cease to be gregarious.
They are also very different in appearance
at different ages. When fully
fed, the larva is of a reddish-grey
colour, spotted with black, with a double row of orange-coloured
warts on each side. There is also a little black hump on each of
the fifth and twelfth segments.

The food plants of this species are sallows (Salix caprea and
S. cinerea), poplar (Populus nigra), and aspen (P. tremula).

Family—Cymatophoridæ

This, the last family of the Bombyces, contains seven species of
moderate size, the larvæ of which are either quite smooth or have
small warty prominences. The seven species are grouped into
three genera, from two of which we shall select a representative.

The Peach Blossom (Thyatira Batis)


Fig. 136.—The Peach Blossom.

The popular name of this pretty little moth is given on account
of the resemblance of the pink
patches of its olive-brown fore wings
to the petals of the peach flower.
It is a moderately common moth,
widely distributed in England and
Ireland, and flies during June and
July.

The caterpillar is marbled with
reddish grey and brown, and has
a hump on the third segment, and a smaller prominence on each[Pg 238]
of the segments six to ten inclusive. It feeds on the bramble
(Rubus fruticosus) during August and September, and spends the
winter in the chrysalis state, inclosed in a loose cocoon among the
dead leaves at the root of its food plant.

The Yellow-horned (Asphalia flavicornis)

This is one of the earliest of our moths, appearing on the
wing in March, when it may be
attracted by means of sugar
placed on the bark of the birch
(Betula alba).


Fig. 137.—The Yellow-horned.

The wings are grey, with a decidedly
greenish tinge, crossed by
three dark lines near the base,
and two others, which are zigzag,
just outside the centre. Between
these two sets of lines is a conspicuous round pale spot. The
hind wings are greyish brown, darker along the hind margin.

The larva, which feeds on the above-named tree, is pale greenish,
with both white and black dots. It rolls itself up in a leaf, and
seldom ventures out of the retreat thus formed. It is fully fed in
July or August.[Pg 239]


CHAPTER XIX

THE NOCTUÆ

We have already noticed that several of our moths fly by day;
that some come out of their hiding places at dusk, and settle down
again to rest before the deepest shadows of night fall; and that
others prefer the darkest hours of the night. The tribe of moths
we are next to consider includes the greater number (about three
hundred) of our truly nocturnal species, hence the name that heads
this chapter.

They are generally of a somewhat dingy appearance, the prevailing
colours being dull shades of grey, drab, and brown. So
closely, in fact, do certain of them resemble each other, that the
greatest care has to be exercised in the identification of species—a
task that is rendered still more difficult by the variations that we
observe in the tints and markings of certain species.

These moths have generally rather stout bodies. Their fore
wings are somewhat narrow, and, when the insects are at rest,
these are brought close to the body, and the hind pair are folded
up beneath them.

Family—Bryophilidæ

The Marbled Beauty (Bryophila Perla)

Our first family—the Bryophilidæ—contains only four British
species. These are small and slender-bodied moths, whose larvæ
feed in early morning on the lichens that cover stones and old
walls, and conceal themselves by day in holes and chinks and under
stones.

The Marbled Beauty is the only moth of this family that may[Pg 240]
be described as common with us. It is abundant in nearly every
English county, as well as in parts of Scotland and Ireland.


Fig. 138.—The
Marbled Beauty.

Its wings are very pale grey, marked with
a darker bluish grey, as shown in the engraving.
These markings are variable, but the
bases of the fore wings have always a dark
blotch, followed by a patch of pale grey or
white, extending the whole width of the
wing. The moth may be found from the beginning
of July to the middle of September.

The larva feeds from February to April.
It is black above, with a broad orange-bordered stripe down the
back; and its body is covered with small warts, each of which
bears a single hair.

Family—Bombycoidæ

In this family there are sixteen British moths, several of which
are exceedingly common. They are much larger than the Bryophilidæ,
and of a much stouter build. The larvæ are covered with
little hair-bearing warts, and are, indeed, often so hairy that they
may be mistaken for the caterpillars of the Bombyces.

The Grey Dagger (Acronycta Psi)


Fig. 139.—The Grey Dagger.

This is the commonest of all the Bombycoidæ. It may be
found at rest on tree trunks and palings during the daytime
throughout the summer. Its fore wings are pale grey, with four
conspicuous black marks, one of
which—that in the anal angle—resembles
the Greek letter psi (ψ)
placed sideways.

The larva is black or very dark
grey, with a pale yellow line down
the back, and a black hump on each
of the fifth and twelfth segments,
that on the fifth being much larger
than the other. It feeds in the
autumn on lime (Tilia vulgaris), blackthorn (Prunus spinosa),
whitethorn (Cratægus oxyacantha), fruit trees, and various other
trees, shrubs, and herbs.[Pg 241]

The moth called the Dark Dagger (Tridens) is hardly to be distinguished
from Psi. It is not really any darker, and its markings
are almost exactly similar; but the larva is very different.

The Poplar Grey (Acronycta megacephala)

This is also a very common moth, to be found in all the southern
and midland counties, wherever poplars abound, during June and
July.


Fig. 140.—The Poplar Grey.

Its fore wings are grey, marbled with a very dark grey. A little
inside the middle of these wings, near the costa, is a round spot
with a dark centre. This spot is
represented in a large number of
the Noctuæ, and is known as the
orbicular. It will be observed
that in the present species it is
very distinct.

The caterpillar is dark grey,
with a line of black dots down the
back; and it has a number of
little warts, bearing hairs. On the back of the eleventh segment
is a rather large pale spot. It feeds during August on various
species of poplar, and changes to a chrysalis in a crevice of the
bark.

The Figure of Eight (Diloba cæruleocephala)


Fig. 141.—The Figure of Eight.

The fore wings are brownish grey. Near the middle of the
wing, but nearer the costa than the inner margin, are two whitish
spots that resemble the figure 8. The hind wings are dull brownish
grey, with darker wing rays, and a
dark spot near the centre.

This moth is common in all parts,
and flies during September.

The caterpillar emerges from the
egg in spring, and is fully grown in
May or June. It is of a very pale
colour—yellowish or greenish—with a
broad and broken yellow stripe down
the back, and a bluish or greenish
stripe on each side. Its head is blue (hence the specific name)
with two black spots. It feeds on the hawthorn (Cratægus oxyacantha)[Pg 242]
and various fruit trees; and on the twigs of these (especially
the hawthorn) the little clusters of eggs may be seen during
the winter.

Family—Leucaniidæ

In this family we have a number of rather small moths, with,
generally, no markings on their wings, save, perhaps, a few dots or
streaks.

Their larvæ feed principally on grasses and reeds, and change to
the chrysalis state either in a cocoon among the food plants, or
under the surface of the ground.

Several of these insects are very common, and most of them
abound in fens and marshes.

The Brown-line Bright-eye (Leucania conigera)


Fig. 142.—The Brown-line
Bright-eye.

The fore wings are yellowish brown. The ‘brown line’ is a
transverse line parallel with the hind margin, and distant from it
about one-fourth the length of the wing. Another dark brown line,
describing a sharp bend, passes across the wing near the base.
The ‘bright eye’ is a light spot just outside the centre of the wing,
nearer the costa than the inner margin.
This is another of those marks that
occur very constantly in the wings of
the Noctuæ. It lies beyond the orbicular
spot, and is usually somewhat
kidney-shaped, and is consequently
named the reniform.

The caterpillar is yellowish or greyish,
with a pale dorsal line edged with
black. On each side of this is a broad
black line, below which is a yellow line edged with black, then a
whitish stripe, next a yellow line edged with black on the upper
side, and lastly a broad brownish line, just above the spiracles,
edged with black on both sides. It feeds on couch grass (Agropyron
repens
) and various other grasses, and is fully grown in
May.

The moth flies in July and August, and is common throughout
the United Kingdom.[Pg 243]

The Smoky Wainscot (Leucania impura)

This same genus includes a number of moths, very similar in
general appearance, and popularly known as the ‘Wainscots.’ Of
these we shall take two examples.


Fig. 143.—The Smoky
Wainscot.

The first is the Smoky Wainscot,
so called from the dark smoky tint
of the hind wings. Its fore wings
are wainscot brown, with lighter rays;
and they each have three black dots arranged
in the form of a triangle, one
in the centre, and the other two between
this and the hind margin.

The caterpillar is yellowish, with a
fine white line down the back. The
spiracles are red, and inclosed in black rings. It feeds on sedges
(Carex) from March to May.

The moth is on the wing from June to August.

The Common Wainscot (Leucania pallens)


Fig. 144.—The Common
Wainscot.

This moth is very much like the last. The fore wings exhibit
the same three dots, but it may be
distinguished by the pale colour of the
hind wings.

The larva feeds on various grasses
in March and April. It is of a pinkish
grey colour, with two rows of
black dots on each side of the dorsal
line. There are also three stripes
along the side, two of which are
brownish and the other grey.

The moth is common everywhere from June to August.

The Bullrush (Nonagria arundinis)

Our last example of this family is the Bullrush, a moth that is
common in all parts where its food plant abounds.


Fig. 145.—The Bullrush.

It is much larger than the two preceding species. The fore
wings are yellowish brown, with three parallel transverse lines of[Pg 244]
black spots. The hind wings are whitish, tinged with brown near
the hind margin.

The caterpillar is of a dull pinkish colour, with a shining
brownish plate on the
second segment. The
spiracles are black. It
feeds inside the stems
of the reed-mace (Typha
latifolia
), and
changes to a chrysalis
within the gallery it
has excavated, after
making a hole through
which it can escape
when it attains the perfect
form.

The caterpillar may
be found in May and June, the chrysalis in August, and the moth
in September.

Family—Apameidæ

This large family contains no less than forty-four British species,
many of which are exceedingly common; and of the others only
about half a dozen can be regarded as rare.

Most of them are of medium size, and with one or two exceptions
are dressed in rather dingy garbs; but, although the ground
colours are dull, the various markings of the wings are sharply
defined. They may be searched for on palings and the bark of trees
by day, at which time they repose with their wings sloping like the
sides of the roof of a house. Some are easily attracted by lights,
and others partake freely of the entomologist’s ‘sugar.’

The larvæ have small retractile heads, and feed on low-growing
plants, keeping themselves well concealed on the lower leaves close
to the ground.

The Frosted Orange (Gortyna Ochracea)


Fig. 146.—The Frosted
Orange.

We commence with one of the brightest members of the family,
the Frosted Orange. Its fore wings are dark yellow or ochreous,
with distinct brown markings, the chief of which are two broad[Pg 245]
transverse bands. The orbicular spot is pale yellow and very distinct.
The hind wings are dingy yellow. This moth flies from July
to September, and is easily attracted
by a light at night. It is common
everywhere.

The larva is yellow, dotted with
black, with a brownish plate on the
second segment. It feeds inside the
stems of a number of plants, including
the marsh thistle (Cnicus
palustris
), musk thistle (Carduus
nutans
), burdock (Arctium minus),
mullein (Verbascum thapsus), foxglove
(Digitalis purpurea), and elder (Sambucus nigra). When
about to change to the chrysalis it eats nearly to the surface of the
stem, leaving only a very thin and transparent layer of the epidermis
to cover the hole through which it is to escape when it
becomes a moth.

The caterpillars are to be found in June, and the chrysalides in
July.

The Flame (Axylia putris)

This also is a pretty insect, but much smaller than Ochracea. It
is common in most parts, and may be seen flying in weedy and
waste grounds at dusk during June and
July.


Fig. 147.—The Flame.

The fore wings are pale pinkish brown,
with dark brown along the costa, and two
patches of the same colour on the hind
margin. There is also a double line of
small brown dots parallel with the hind
margin.

The larva is brown, with one yellow and two white dots on each
segment. There is also a triangular dark patch on each of the fifth
and sixth segments. It feeds during August on the stinging nettle
(Urtica dioica), and various other low herbs.

The Light Arches (Xylophasia lithoxylea)


Fig. 148.—The Light Arches.

The fore wings of this species are very light ochreous, with a
light brown patch on the middle of the costa, and patches of the[Pg 246]
same colour along the hind margin; also a row of small black dots
parallel with the same
margin. The hind wings
are pale ochreous: they
are brownish along the
hind margin, and have
a light fringe.

The moth is very
common in waste places,
and flies in June and
July.

The caterpillar is of
a dirty white colour, dotted with black, and has a black head. It
feeds on the roots of grasses in May.

The Flounced Rustic (Luperina testacea)


Fig. 149.—The Flounced
Rustic.

The fore wings are greyish brown, with darker umber-brown
markings. These latter are variable,
but the most conspicuous is a series
of dark crescent-shaped spots almost
parallel with the hind margin, and
immediately outside these is a series
of paler crescents.

The caterpillar is dull flesh-colour,
with a brown head, and a brownish
plate on the second segment. It feeds
on the stems of grasses.

The moth is common throughout the British Isles, and flies in
August and September.

The Cabbage Moth (Mamestra Brassicæ)

Whatever be your methods of moth collecting, you are sure to
meet with Brassicæ in abundance. They swarm round the insect
hunter’s sugar in such numbers as to become a positive nuisance.
They are also attracted by light. During the day they may be seen
at rest on palings. The caterpillar is even better known, and with
reason, for it is fearfully destructive to our vegetables and even our
flower beds. It burrows into the hearts of cabbages, filling the
galleries it makes with its excrement, often leaving no very[Pg 247]
visible outward signs of its presence within. But its ravages
are by no means confined to cabbages. It eats with more or less
relish almost every vegetable
and flowering plant of our
gardens, and is equally partial
to the various herbs of the field.


Fig. 150.—The Cabbage Moth.

The fore wings of the moth
are dingy brownish grey, marbled
in a very confused manner
by darker markings. The
reniform spot is very distinct,
the orbicular less so. A light
zigzag line runs parallel with the hind margin. It flies in June
and July.

The larva feeds later in the season, and changes to the chrysalis
beneath the soil in the autumn. It is of a dark grey colour, with a
darker line on the back, and a lighter one along the spiracles, which
are white.

The Dot (Mamestra Persicariæ)


Fig. 151.—The Dot.

The conspicuous white reniform spot on the very dark marbled
fore wings is always sufficient for the identification of this species.

This moth is out in June and July; and during the latter month
lays its eggs on the elder (Sambucus
nigra
), and the various low
plants that supply the larva with
food.

The larva is greenish or greyish,
sometimes with a reddish
tinge, with a light line down the
back. The twelfth segment is
humped, and there are dark V-shaped
marks on the back of segments
five to twelve inclusive. It is full grown in September, and
burrows into the ground to undergo its change to the chrysalis, in
which state it remains throughout the winter.

The Rustic Shoulder-knot (Apamea basilinea)


Fig. 152.—The Rustic
Shoulder knot.

The fore wings of this species are pale ochreous grey, with light
brown markings; and there is a short dark streak in the middle of[Pg 248]
the base, from which feature the specific name (Basilinea) is
derived. The hind wings are of a similar colour, but shading into
a dark smoke colour at the hind
margin.

The caterpillars feed at first on
the grains of wheat, on the ears of
which the moth deposits the eggs
in June. At harvest time they remain
hidden among the husks, and
are often threshed out in large
numbers by the blows of the flail.
The cold weather soon overtakes
them, and they then spin a cocoon in which to pass the winter.
On the approach of spring they come out again, and feed by night
on various low plants, hiding themselves among the roots by day.
In March they are full grown, and change to brown chrysalides
beneath the surface of the ground.

The moth flies in June, and is one of the commonest and most
destructive of our Noctuæ.

The Marbled Minor (Miana strigilis)

The next three genera (Miana, Phothedes, and Celæna) include
seven small moths known as the ‘Minors.’ The commonest of
them is the Marbled Minor, which is to be
found in abundance everywhere during June
and July.


Fig. 153.—The Marbled
Minor.

This species is very variable, but the fore
wings are usually dark brown, marbled with
a lighter colour—white or grey. There is
generally an irregular white or pale grey
band crossing the wings parallel with the
hind margin, and two white marks on the inner margin, halfway
between this band and the base. There is also a deep black blotch
across the middle of the wing.

The caterpillar is greyish or greenish with paler lines and black
spiracles. It feeds on grasses in March and April, and changes to
a chrysalis under the ground in May.

Family—Caradrinidæ

There are only ten British species in this family, two of
which are rare; and most of the others are particularly dingy.[Pg 249]
The transverse lines so often seen on the fore wings of Noctuæ are
generally well marked. The larvæ have short stiff bristles, and
feed on low plants; they undergo their changes in an earthen
cocoon under the ground.

The Mottled Rustic (Caradrina Morpheus)

We select as our type of this family the Mottled Rustic—a
common moth that may be procured from June to August. Its
fore wings are brownish grey, with
darker lines and spots; the hind wings
are almost white, but darker at the tip.


Fig. 154.—The Mottled
Rustic.

The caterpillar is brownish grey, with
a row of triangular spots on each side of
the back. It is very sluggish, spending
the greater part of its existence among
the roots of low plants. It feeds throughout
the winter, except during severe
weather, and is full grown in April. The food plants include teasels
(Dipsacus pilosus and D. sylvestris), hedge bedstraw (Galium Mollugo),
orpine (Sedum Telephium), sallows (Salix), and various
other plants.

The chrysalis may be dug out in May.

Family—Noctuidæ

A glance at our list of British Noctuæ (Appendix I) will show
that this family contains nearly fifty species and only three genera.
It includes several very common moths that frequent our gardens
and are to be met with during almost every summer evening
ramble.

Most of the species are very dingy, but the half-dozen that
comprise the genus Triphæna are characterised by the bright
colouring of the hind wings. The fore wings are narrow and more
or less glossy, and overlap to a greater or less extent when the
insects are at rest; and the hind wings are folded and completely
hidden beneath them.

The larvæ are rather thick and smooth, and generally of very
dingy colours. They feed on low plants, often confining their
ravages to the roots, and generally lie well concealed close to the
ground or under the surface.[Pg 250]

The pupæ are brown, smooth, and shining, and are usually
inclosed in earthen cocoons.

We shall briefly notice a few members of each of the three
genera.

The Turnip Moth (Agrotis Segetum)

This is another of those destructive insects that attack vegetable
and flower gardens, often doing so much damage to our crops as to
become quite a nuisance to cultivators.


Fig. 155.—The Turnip Moth.

The moth is decidedly dingy. Its fore wings are brown, clouded
with a darker tint. The hind wings are almost white, sometimes
with a brown hind margin.

In June it lays its eggs on the stems of young plants, generally
very close to the ground. As soon as the young caterpillars emerge
they commence feeding on the
lower parts of the stems, or burrowing
deeply into the larger succulent
roots. When the larvæ have completed
their work of destruction in
this way, they change to brown
chrysalides in the ground. Some
undergo this change in October, and
shortly after give rise to a second
brood of moths; but most of them remain in the caterpillar state
throughout the winter, and, contrary to the general rule with
hybernating larvæ, continue to feed almost throughout the winter
months, and change to the chrysalis in the following May.

The caterpillar grows to a large size. It is of a greyish or
greenish colour, with a paler line on the back, a light brown line
on each side of this, black spots between these lines, and black
spiracles.

The Heart and Dart (Agrotis Exclamationis)

The destructive work of Segetum is assisted by similar operations
of the Heart and Dart, the larva of which feeds voraciously
on the roots of several of our cultivated vegetables, though
the present species does not entirely confine its ravages to the
farmer’s crops, but attacks the roots of many low-growing herbs.


Fig. 156.—The Heart and
Dart.

The fore wings of the moth are light brown, generally with
a reddish tinge. The darker markings include a large and very[Pg 251]
distinct reniform spot, a less distinct orbicular, and a conspicuous
longitudinal blackish streak near the base of the wing known as the
claviform. Beyond the reniform
a curved and zigzag dark line
crosses the wing. The hind wings
of the male are very pale, those
of the female darker, with a whitish
fringe.

The moth flies from June to
August, and is common everywhere.
The caterpillar feeds in
the autumn, and reaches its full
size in October; but it is said to
feed at intervals throughout the winter. Its colour is dingy brown
or grey, with paler lines on the sides. The spiracles are black, and
there are black dots on the sides.

The Garden Dart (Agrotis nigricans)

This is another dingy moth, whose general appearance is so
unattractive that the tyro might be inclined to neglect it. But it
must not be omitted from our selection on that score, for our main
object here is to give the beginner
an acquaintance with those species
that are most likely to be captured
in the earlier part of his career, and
this moth is certainly one of those
that may be described as ‘abundant
everywhere.’


Fig. 157.—The Garden Dart.

Its fore wings are dull dark brown,
often tinged with red, and clouded
with black. The reniform spot is
pale, the orbicular spot less distinct, and between the two there is
generally a rhomboidal dark spot. There is also a short dark streak
near the base of the wing, and a black spot before the orbicular.
The hind wings are pale, but smoky towards the hind margin.

The caterpillar is brown and shining, with a fine pale line on
the back, and a double white stripe below the spiracles. It is also
dotted with black. It is exceedingly destructive, feeding on clovers
(Trifolium pratense and T. repens) and various low plants in May
and June.

The moth flies from June to August.[Pg 252]

The Flame Shoulder (Noctua plecta)


Fig. 158.—The Flame
Shoulder.

As our example of the next genus we take the Flame
Shoulder, a rather small moth, easily identified by the broad
yellowish-white streak along the costa of the reddish-brown fore
wings. The orbicular and reniform spots
are margined with white, and a thin white
streak runs from the base of the wing to
the former. The hind wings are white.
This moth flies in July, and is common
throughout Great Britain.

The caterpillar is reddish brown, with
a slender line of white dots on the back,
and a similar line on each side. The body
is smooth and velvety, and is netted and dotted all over with dark
brown. It feeds on the lady’s bedstraw (Galium verum), sweet
woodruff (Asperula odorata), and many other low plants; and
is full fed early in July.

The Lesser Broad Border (Triphæna ianthina)

We now come to the third and last genus (Triphæna) of this
extensive family, a genus which includes six interesting moths,
with bright orange or yellow hind wings. Of these we shall take
three examples.


Fig. 159.—The Lesser Broad
Border.

The first of them—the Lesser Broad Border—has fore wings of
a rich reddish or violet brown, with paler markings. The hind
wings are bright orange, with a
broad marginal band of black.

It is a common moth, particularly
in the south-western counties,
and flies during July and August.

The caterpillar is of a dingy yellowish
or greenish grey, with a light
line down the back, and two black
spots on each side of segments nine
to twelve inclusive. It feeds throughout
the winter by night on dead nettles (Lamium purpureum and
L. album), primrose (Primula acaulis), whitethorn (Cratægus
oxyacantha
), blackthorn (Prunus spinosa), and various low plants;
and may sometimes be seen in flower gardens. It is full grown
in April.[Pg 253]

The Lesser Yellow Underwing (Triphæna Comes)


Fig. 160.—The Lesser
Yellow Underwing.

This insect is very similar to the last, but is larger. The
fore wings are also of a greyish or ochreous brown, and the black
margin of the hind wings is proportionately
narrower.

It is more abundant than Ianthina;
in fact it is to be found
everywhere in plenty during the
month of July.

The caterpillar is yellowish
brown. On the back of each of
the eleventh and twelfth segments
are two conspicuous dark marks.
The spiracles are white, and below
them is a pale brown stripe. It feeds on the foxglove (Digitalis
purpurea
), chickweed (Stellaria media), thrift (Armeria maritima),
and other low plants in the autumn, hybernates during the winter,
and attacks sallows (Salix Caprea and S. cinerea) and whitethorn
(Cratægus oxyacantha) as soon as the buds appear in the spring.
It is full grown in April, and then changes to a chrysalis on the
surface of the earth.

The Large Yellow Underwing (Triphæna Pronuba)

This is by far the commonest moth of the genus, and may be
found everywhere, in town and country, from June to August. It
is represented on Plate XI (fig. 1), but its fore wings are very variable,
sometimes a cold dingy grey, but often of an exceedingly rich
and warm brown. On the costal margin, not far from the tip, there
is always a small black spot, which will serve to distinguish it from
Comes.

The caterpillar (fig. 21) feeds throughout the winter on the roots
of almost every plant in our gardens; and, during the warmer
weather of the autumn and spring, on stems and leaves. It is full
grown early in the summer, and then changes to a chrysalis in the
ground. Its colour is dirty yellowish or greenish grey, with a row
of dark spots on each side.[Pg 254]

Family—Amphipyridæ

The Gothic (Mania typica)

The above family contains only four British species, two of
which we shall briefly consider.


Fig. 161.—The Gothic.

The first of these is the Gothic—a very common moth that may
be seen everywhere about midsummer. Its fore wings are brown
with darker marblings, and
there are numerous lighter
markings which may be easily
made out by reference to the
accompanying woodcut.

The caterpillar is smooth
and velvety, of a dull brown or
greenish colour, with darker
dorsal and side stripes. The
latter are crossed obliquely by
a series of whitish lines. It
feeds on fruit and other trees
in clusters when very young in early autumn, and afterwards
descends and feeds on low plants. It hybernates in the winter, and
feeds again on low plants in the spring. When full grown it burrows
into the soil to undergo its changes.

The Old Lady (Mania Maura)


Fig. 162.—The Old Lady.

This fine moth is so very different from the last in appearance
that the reason
for placing the two
in the same genus
is not apparent
till the earlier
stages and life history
have been
studied. All its
wings are very
deep brown; the
front pair has a
darker band containing
the orbicular
and reniform spots, and the hind pair a lighter band across the
middle.

[Pg 255]

It is a common moth, often to be found at rest by day in outhouses
and sheds. It flies in July and August.

The caterpillar is dark purple or umber brown, with darker and
lighter markings. It feeds in the autumn on fruit trees, and
hybernates during the winter. In the spring it feeds again on low
plants, and changes to a chrysalis in May under the ground.

Family—Orthosiidæ

This is a large family of over thirty species, most of them of
rather small size, which make their appearance, with two exceptions,
either in early spring or in late autumn, often attracted in the former
season by the sallow blossom, and in the latter by ivy bloom.

Several of them are very common insects, that are almost sure
to be taken by a young collector during his first season.

The fore wings of these moths are more or less pointed at the
tip, and the usual lines and spots are generally distinct. The males
may be distinguished from the females by their antennæ, which are
always more or less ciliated.

The caterpillars are smooth and velvety, and feed by night; and
the pupæ are inclosed in cocoons constructed of earth and silk.

The Common Quaker (Tæniocampa stabilis)

Several of the species of the family are known popularly as
Quakers, the commonest of which—Stabilis—is abundant in all
parts.


Fig. 163.—The Common
Quaker.

Its fore wings are grey, with generally either an ochreous or
reddish tinge. The orbicular and
reniform spots are outlined with
a paler colour, and there is a pale
transverse line parallel with the
hind margin, outside which is a row
of indistinct black spots. The hind
wings are greyish brown.

The caterpillar is green and
velvety, with a yellowish line on
the back and on each side; and a
yellow band crosses the back of the twelfth segment transversely.
It feeds during June and July on oak (Quercus Robur) and elm
(Ulmus campestris), and changes to a chrysalis in August on the
surface of the ground. In this state it remains throughout the
winter, and the moth emerges in March or April.[Pg 256]

The Chestnut (Cerastis Vaccinii)

Unfortunately our space will not allow us to notice the whole of
even the very common moths, so, passing over a few with great reluctance,
we come to the familiar Chestnut, which may be seen at
large in October and November, and sometimes even in December,
and again appears, after a rather short
period of hybernation, in February
and March.


Fig. 164.—The Chestnut.

The fore wings are reddish brown,
with darker wavy lines. The orbicular
and reniform spots have pale outlines,
and the lower half of the latter is very
dark grey. The hind wings are smoky
grey, with generally a pale band beyond the middle.

The caterpillar is dark brown, with very indistinct lighter lines.
The spiracles are black, and inclosed in a yellowish grey stripe. It
feeds during June and July on the elm (Ulmus campestris), oak
(Quercus Robur), and sallow (Salix caprea), and various low
plants.

The Pink-barred Sallow (Xanthia Flavago)

This moth is not nearly so common as the preceding species,
but has been taken more or less in all parts of England.



Fig. 165.—The Pink-barred Sallow.

Its fore wings are orange yellow,
with purplish markings arranged as
represented in fig. 165. The hind
wings are yellowish white.

The caterpillar is brown, with a
lateral stripe formed by numerous red,
yellow and white dots. It feeds on
sallow (Salix caprea) and various low
plants.

It is full grown in June, and the moth appears in September.

Family—Cosmiidæ

The Dun-bar (Calymnia trapezina)

Our example of this family is the Dun-bar, common everywhere
during July and August.


Fig. 166.—The Dun-bar.

Its fore wings are greyish ochreous, with a darker band across
the middle. On each side of this band is a white line margined with[Pg 257]
dark grey, and there is a row of black spots along the hind margin.
The hind wings are smoky brown, becoming paler towards the base.

The caterpillar feeds on oak (Quercus Robur), hornbeam (Carpinus
Betulus
), and birch (Betula alba),
and may be found in abundance during
May and June. It is green, with dark
spots, and white lines on the back and
sides. Although it partakes of the leaves
of the above-named trees, yet its chief
food seems to be other caterpillars, for it
devours these with a savage greediness
that is simply astonishing. It will chase
an unfortunate caterpillar, seize it by the neck with a fatal grip,
and rapidly devour it. Its chief prey seems to be the larva of the
Winter Moth (Brumata).

Family—Hadenidæ

Nearly fifty British Noctuæ are included in the family
Hadenidæ. They are of variable dimensions, and differ much in
the brightness of their colours, some being very dingy, and others
gaily tinted. Their antennæ are rather long; and when at rest
the wings slope from the back like the sides of a roof.

The larvæ are smooth, and not very thick; and there is sometimes
a hump on the twelfth segment. The pupæ are brown and
shiny, and are inclosed in earthen cocoons beneath the surface of
the soil.

The Broad-barred White (Hecatera serena)


Fig. 167.—The Broad-barred White.

Although not gaily coloured, this is a pretty little moth, there
being a bright contrast between the white ground and the grey
markings of the wings. It is common
in the south of England, and seems to
be plentiful in and around London.

The caterpillar is of a dingy greenish
colour, with a yellowish stripe on each
side of the back; and there are two distinct
dots on the back of each segment.
It feeds during July and August on sow-thistles
(Sonchus oleraceus and S. arvensis),
sleepwort (Lactuca virosa), and hawkweeds (Hieracia).

The moth flies in June and July.[Pg 258]

The Marvel-du-jour (Agriopis Aprilina)

The Marvel-du-jour is decidedly a beautiful moth—quite an exception
among the Noctuæ in this respect, and it is withal both
common and widely distributed. We need not describe it, since it
is represented on Plate XI (fig. 2), and can hardly be mistaken for
any other species.

The caterpillar is dull green, often tinged with red. The dorsal
line is broad and dark, and interrupted by a series of very light
lozenge-shaped spots. It feeds on the oak in May and June, and is
full grown in the latter month. It then burrows into the earth at
the foot of the tree, and there constructs a fragile earthen cocoon
previous to changing to a chrysalis.

From July to September the chrysalides may be obtained in
plenty by breaking up the sods at the roots of oaks, and the perfect
insect may be found toward the end of September and throughout
October.

The Small Angle Shades (Euplexia lucipara)

This pretty little moth is represented in fig. 3 of Plate XI. It
is very common throughout the country, and may be seen in June
and July.

The caterpillar is thickest on the twelfth segment, and gradually
tapers from this towards the head. Its colour is pale green, with a
white stripe just below the spiracles, which are black. On each
side of the back are a number of oblique lines, which meet in the
middle line, thus forming a series of V-shaped marks pointing
towards the tail. It feeds on the common bracken fern (Pteris
aquilina
), foxglove (Digitalis purpurea), and the male fern (Lastræa
Filix-mas
), in August and September.

The Angle Shades
(Phlogophora Meticulosa)


Fig. 168.—The Angle Shades.

This moth is so common
and so widely distributed
that it is almost
sure to be taken by the
young collector during
his first season. Its wings
are scalloped on the hind margin, and their colour light ochreous,
often tinged with pink or olive green, and marked with dark[Pg 259]
brown as shown in the illustration. It is double brooded, the first
brood appearing in May and June, and the second in September
and October.

The caterpillar is green or olive brown, and thickly covered
with white spots. It feeds on groundsel (Senecio vulgaris) and
many other low plants, the first brood throughout the winter from
November to April, and the second in July and August.

The Grey Arches (Aplecta nebulosa)


Fig. 169.—The Grey Arches.

The fore wings of this moth vary from greyish white to a rather
dark smoky tint. The markings are of a darker colour, and are
also subject to considerable variation. The orbicular and reniform
spots are large, and paler than the ground colour; and several zigzag
or scalloped lines,
more or less distinct,
cross the wings transversely.

The larva is brown,
with a lighter line down
the back. On each of the
segments five to eleven
is a dark lozenge-shaped
spot, bisected by the
dorsal line; and on the
second segment is a shining plate and a triangular mark. It feeds
on the dock (Rumex), and various other low plants during the
autumn; and, after its hybernation, on the leaves of the sallow
(Salix Caprea), birch (Betula alba), and whitethorn (Cratægus
oxyacantha
). It is full grown in May, when it burrows into the
ground to undergo its metamorphoses.

The moth flies during June and July, and is common in nearly
every part of Great Britain. Large numbers may be obtained by
searching fences and tree trunks about midsummer.

The Shears (Hadena dentina)


Fig. 170.—The Shears.

The Shears is another very common moth of the same family.
The ground colour of the fore wings is very variable, but is generally
a lighter or darker shade of grey. Sometimes, however, it
has a very decided brownish tinge. Across the centre of the wing[Pg 260]
is a darker band, wider on the costal side, containing the orbicular
and reniform spots, as well as a light patch beneath them, and bordered
on each side by a pale zigzag
line. There is another similar line
near to and parallel with the hind
margin. The hind wings are smoky
grey or smoky brown, darker towards
the hind margin.

The caterpillar is greyish, and has
a series of triangular black spots along
each side of the back. It feeds on the roots of the dandelion
(Taraxacum officinale), and changes to a peculiar spiny chrysalis.

The perfect insect appears to be abundant everywhere, and is
on the wing in June and July.

The Bright-line Brown-eye (Hadena oleracea)

Every collector is sure to meet with this insect during his first
season. The moth is abundant everywhere in June, the caterpillar
may be found feeding in almost every waste and weedy spot in
August and September, and the chrysalis is certain to be turned
over by the pupa digger.


Fig. 171.—The Bright-line Brown-eye.

The fore wings of the perfect insect are reddish brown. The
orbicular spot is usually very indistinct,
being of almost exactly the
same tint as the ground colour, and
surrounded by a very fine whitish
line. The reniform is generally
more conspicuous, a portion of it
being of a light ochreous colour.
Near the hind margin, and parallel
with it, is a white line, bent
sharply into the form of a W, just
on the anal side of the middle.

The hind wings are greyish brown in the base, and dark smoke
colour towards the margin.

The caterpillar is pale green or brown, dotted with both black
and white, and adorned with a bright yellow line just below the
spiracles. It feeds on the nettle (Urtica dioica), dock (Rumex),
and many other low plants; and, according to some observers, on
the elm (Ulmus campestris).[Pg 261]

Family—Xylinidæ

The next family—Xylinidæ—contains twenty British species,
several of which are local, but two or three are abundant and
widely distributed.

The transverse lines that so often cross the wings of the Noctuæ
are nearly or entirely absent in this family, and longitudinal lines
take their place. When the insects are at rest the wings are folded
rather closely, the outer pair being arranged like a roof with a very
gentle slope. The bodies of the perfect insects are very stout,
particularly in the thorax, and thus present a rather powerful
appearance.

The larvæ are smooth, and generally brightly coloured, and
feed principally on low plants. The chrysalides are generally
inclosed in cocoons on or beneath the ground, and are often provided
with spines or bristles on the under side.

We shall select two members of this family.

The Early Grey (Xylocampa Areola)

One of the first of the Noctuæ to greet us in the spring is the
Early Grey, which may be found resting on fences in April, and,
if the season is mild, in March.


Fig. 172.—The Early Grey.

Its fore wings are light grey, often
tinged with rose pink, and marked
with dark grey. The orbicular and
reniform spots are very distinct, and
surrounded by a pale line; they are
both united at their lower edges. Along
the hind margin is a series of dark
spots. The hind wings are pale yellowish
grey, with a darker central
spot, a central transverse darker line, and a darker line along the
hind margin.

The caterpillar is yellowish grey. The dorsal line is lighter,
and passes through a brownish spot on the eighth segment. It
feeds on the honeysuckle (Lonicera Periclymenum) in July and
August, being full grown towards the end of the latter month.

The Shark (Cucullia umbratica)

The Shark is a very common moth, to be found everywhere on
palings in June, but the colour of its wings so closely resembles[Pg 262]
that of oak and other light-wood fences that detection is not so
easy as with most other moths.


Fig. 173.—The Shark.

The fore wings are grey, and marked with longitudinal dark
lines, the principal of which is a line from the middle of the base
to about the centre of
the wing. The wing
rays are also darker
than the ground
colour. The hind
wings are greyish
white or brownish
grey.

The caterpillar is
very dark brown, with
orange spots on the
back and along the
spiracles. It feeds on
sow-thistles (Sonchus oleraceus, S. palustris, and S. arvensis) and
sleepwort (Lactuca virosa) at night from July to September, and
hides during the daytime among the leaves that lie close against
the ground. When disturbed it does not roll into a ring or feign
death like many others of its kind, but wriggles about most vigorously
as if to repel its foe.

Family—Gonopteridæ

The Herald Moth (Gonoptera Libatrix)

The above-mentioned family is so called on account of the
angular margins of the wings, especially the fore pair. It contains
only one British species, the Herald (Plate XII, fig. 1), a moth
that is common everywhere in August and September. It hybernates
in the perfect state, and the hybernated specimens may be
seen in the spring time, from March up to the end of May or the
beginning of June.

Its fore wings are reddish grey, thickly spotted and streaked
with brown. Transverse whitish lines divide the base into three
parts of nearly equal widths. The basal and central divisions are
tinged with orange; and there is a small white spot in the base
close to the thorax, also another near the centre of the wing. The
hind wings are brownish grey.[Pg 263]

The caterpillar is green and velvety, with a whitish stripe on
the side, and yellow spiracles. It feeds on willow (Salix alba)
and sallow (Salix caprea); and when full grown, about the end
of June, it spins a white silken cocoon between leaves of its tree,
and changes to a very dark chrysalis.

Family—Plusiidæ

The most peculiar feature of the moths of this family is the
tufts of hair that stand up perpendicularly on the top of the thorax.
The abdomen also is crested, and the fore wings of several species
have smooth patches that display a brilliant metallic lustre.

Most of the larvæ may be described as semi-loopers, for their
claspers number only three pairs, and when they walk their backs
are considerably humped, somewhat after the fashion of the Geometræ.
Some of them further imitate the Geometræ in their
position of rest, holding on by their claspers only, with body
straightened out at an angle with the leaf or twig on which they
support themselves.

Unlike the majority of the Noctuæ, they do not descend to the
ground when about to change, but spin a silken cocoon among the
food plants.

The Burnished Brass (Plusia Chrysitis)


Fig. 174.—The Burnished Brass.

One of the commonest of the Plusiidæ is the Burnished Brass,
so called on account of the large patches of bright golden green on
the fore wings. The hind margin of these wings is very gracefully
curved, and bordered with brown. A
brown blotch fills the base of the wing,
and the remaining area is of a beautiful
metallic greenish yellow, broken by
two large brown blotches, one on the
costal and the other on the inner margin,
which closely approach each other
and sometimes meet.

This moth is very common everywhere,
and is one of the frequent
visitors to our flower gardens from June to August.

The caterpillar is thickest at the twelfth segment, and tapers
from this point. Its colour is pale green. It has no longitudinal
stripes on the back, but each segment is adorned with four or six[Pg 264]
oblique white marks. Just above the spiracles is a white stripe.
It feeds on the dead nettle (Lamium album), stinging nettle
(Urtica dioica), and burdock (Arctium minus), and is full grown
in June.

The Silver Y (Plusia Gamma)


Fig. 175.—The Silver Y.

Our second example of this family is the Silver Y, which may
be found in abundance everywhere from June to October. Its fore
wings are of a shiny grey colour, beautifully marbled with a rich
dark brown; and just below the orbicular spot is a brilliant silvery
spot, in form something like the Greek letter γ placed obliquely.
The base of the hind wings is
grey; along the margin is a
broad and dark smoky brown
band, and the fringe is very
light grey, barred with the dark
tint of the band. This moth is
commonly driven out of its
hiding places among low plants
as we walk in waste places, and
when thus disturbed it takes a
short and rapid flight, generally disappearing so suddenly among
the herbage that it is difficult to locate it correctly.

The caterpillar is thickest at the twelfth segment, and tapers
gradually from this point towards the head. Its body is green,
with several thin longitudinal white stripes, and a thin yellow
stripe along the spiracles. It may be found from June to October,
feeding on many kinds of low plants.

Family—Euclidiidæ

The Mother Shipton (Euclidia Mi)

Passing over a few small and less important families, we come
to the Euclidiidæ, which contains only two British moths. One
of these is the Mother Shipton, a very common insect that flies in
June.

The fore wings of this species are very dark brown with whitish
markings. The latter include a peculiarly tortuous line, the character
of which will be made out more easily from our illustration (Plate
XI
, fig. 4) than from a written description. The hind wings are[Pg 265]
also very dark brown, and rather prettily spotted with an ochreous
tint.

The caterpillar is pale grey, with four white stripes, and has
only three pairs of claspers. It feeds in May on clovers (Trifolium
pratense
and T. repens) and other plants.

Family—Catocalidæ

This family contains only four British species, but these few are
very striking moths. They are of large size; and, unlike the
Noctuæ generally, the chief adornment is reserved for the under
wings. When at rest, the outer or fore wings completely hide the
other pair, and then their general appearance is dull, though if
closely examined it will be observed that these outer wings are
really beautifully marbled with shades of grey.

The caterpillars of this family are very peculiar creatures. Their
bodies are convex above and flattened beneath; and if disturbed
as they rest on the bark of a tree, instead of leaving their hold and
rolling into a ring like so many other larvæ of Noctuæ, they apply
themselves the closer, and hold on as if to defy our attempts to
remove them. Another peculiarity of these larvæ is the possession
of fleshy projections along the sides, just above the legs. They feed
on the leaves of trees, and when about to rest they descend to the
trunk, and there remain protected by their imitative colouring,
detection being rendered even more difficult by the close application
of their flattened under surface to the bark. Before changing
to the chrysalis state, they spin a light cocoon among the leaves or
on the bark.

The Clifden Nonpareil (Catocala Fraxini)

This is the largest of the family, and, indeed, of all British
Noctuæ. The fore wings and thorax are light grey, dotted and
marbled with darker grey (see fig. 5, Plate XI); and the thorax
and abdomen are banded with black and greyish blue.

The young entomologist can hardly expect to meet with this fine
insect, for it is very rare, and it is only occasionally that a specimen
is seen in Britain; but its characteristics are so striking that we have
endeavoured to find it a place here. Reputed British specimens of
Fraxini command the price of a few pounds each, but specimens
from the other side of the Channel may be obtained for a few pence.
With such rarities we should advise a young entomologist to purchase[Pg 266]
the foreign specimen rather than adopt the two other alternatives—give
an exorbitant price for a supposed Britisher, or else remain a
stranger to the gem, but all foreign specimens should be labelled
according to their nationalities.

The Red Underwing (Catocala Nupta)


Fig. 176.—The Red Underwing.

The other three members of the family are very similar in
appearance, the fore wings of all being marbled with shades of
grey, relieved by touches of black and brown; and the hind wings,
red or crimson, give the popular names to the species.

The Red Underwing flies in August and September, and is
common in the southern counties of England, as well as in some
of the midland counties; it may be often seen flying by day
around willows.

The caterpillar is similar in form to that of Fraxini, and when
at rest by day on the bark of its tree it is very difficult to detect, so
closely does it apply itself to the surface, and so perfectly does it
imitate the colour of its surroundings. It feeds on the crack willow
(Salix fragilis), sallow (S. alba), poplar (Populus), and plum
(Prunus), and is full grown in June.

The Dark Crimson Underwing (Catocala Sponsa)

This beautiful insect is represented on Plate XI (fig. 6). It will
be observed that the black band crossing the centre of the hind
wing is rather broad and sharply bent—an important feature, since
it is the most serviceable distinguishing mark between this species
and the Light Crimson Underwing (C. Promissa).[Pg 267]

The caterpillar is similar in form and habits to those of Fraxini
and Nupta, and feeds on the oak. It is full fed about the beginning
of June, when it changes to a chrysalis between leaves which it has
spun together with silk.

The moth flies in July and August, and is common only in
certain oak woods of the southern counties. It is particularly
abundant in the New Forest, where scores may be taken in a
single night by judicious sugaring.

There yet remain a few small families of the Noctuæ, but we
must leave them in order that we may give a proportionate share
of our space to the other great division of the larger moths—the
Geometræ.[Pg 268]


CHAPTER XX

GEOMETRÆ

We have already referred (page 28) to caterpillars that walk by a
series of strides, alternately looping and extending their long and
slender bodies. It is this peculiar characteristic of the larvæ of
the present division that suggested the name Geometræ—a term
that signifies ‘earth-measurers,’ for they appear to measure the
ground over which they travel in terms of their own length. We
have also dealt with the peculiarities of structure in the case of
these caterpillars—peculiarities which adapt them to this mode of
progression; and we have now to make a selection from the various
families of this important division for a more detailed description.

The Geometræ include nearly three hundred species and sixteen
families. The moths have slender bodies and full wings, and
generally rest with the latter outspread. A few, however, repose
with wings erect like the butterflies, and a small number conceal
their hind wings after the manner of the Noctuæ.

Family—Uropterygidæ

The Swallow Tail (Uropteryx sambucaria)

Our first family—Uropterygidæ—has only one British representative,
and that is the well-known Swallow Tail, so common in gardens
and among hedgerows in the south of England. This species
is shown on Plate XII (fig. 2), and the insect is so readily identified
by the conspicuous ‘tails’ on the hind wings that no written description
will be necessary.

The caterpillar is a most peculiar and interesting creature. Its
colour is very variable, being either brown, olive, ochreous, or reddish;
and it is notched or humped in such a manner that it exactly
resembles a twig. This strange imitation is rendered still more remarkable[Pg 269]
by the attitude assumed by the caterpillar when at rest.
It fixes itself to a twig by means of its two pairs of claspers, with
its body standing out at an angle in a perfectly straight posture;
but its head is always supported by means of a very slender and
almost invisible silk fibre. It feeds on a number of plants and trees,
including elder (Sambucus nigra), blackthorn (Prunus spinosa),
whitethorn (Cratægus oxyacantha), bramble (Rubus fruticosus),
honeysuckle (Lonicera Periclymenum), and forget-me-not (Myosotis
arvensis
). It may be found feeding in the autumn, or hybernating
in the crevices of the bark of trees in winter. In April or
May it comes out again; and in June, in which month it is full
grown, it binds together some fragments of leaves, and forms
them into a little swinging hammock in which it changes to a brown
chrysalis spotted with black.

Just at this time it seems to be particularly sensitive. In the
caterpillar state it will strongly resent any kind of disturbance,
and will give a blow to an intruder by suddenly swaying its
body right and left; and while in its hammock a gentle irritation,
such as a puff of wind from the mouth, will set it wriggling in a
furious manner.

Family—Ennomidæ

This family contains about twenty species, several of which rank
among the commonest as well as the most beautiful of the Geometræ.
Their wings are more or less angulated; and the antennæ
are generally pectinated in the males.

The larvæ are generally humped and twig-like; and, as in the
last species, the semblance is increased by the position they assume
when at rest. The number of limbs varies from ten to fourteen, but
where the claspers exceed two pairs, the additional two or four, as
the case may be, are seldom used in walking.

The Brimstone Moth (Rumia luteolata)

As soon as the warm evenings of May set in, this lively and
bright little moth may be seen flitting about among our hedges at
sunset; and it continues with us throughout the whole of the summer,
but is particularly plentiful during the month of June.

The moth itself need not be described, since it is shown on Plate
XII
(fig. 3); but the caterpillar (fig. 25) must receive a passing
notice. It varies considerably in colour, being either green, brown,[Pg 270]
or marbled with a mixture of shades of both these colours. It has
a hump on the back of the seventh segment, and two more on the
ninth, and possesses four pairs of claspers. It feeds on whitethorn
(Cratægus oxyacantha), blackthorn (Prunus spinosa), and the
apple (Pyrus Malus), and may be found on these trees throughout
the summer.

Some believe that there are three successive broods of this insect
each year, but it is doubtful whether this is invariably the rule, since
both the moth and its larva are to be found without intermission
throughout the season.

The Light Emerald (Metrocampa margaritaria)


Fig. 177.—The Light Emerald.

All the wings of this moth are very pale green, and crossed with
a white band which is bordered with a darker green on the inner
side. The fore wings have an additional transverse line just halfway
between the former and the base,
but this one is not so distinct. It
flies in July, and is very widely distributed,
and in some parts is very
abundant.

The caterpillar feeds in September,
and again in May, after hybernation,
on several of our forest trees, including
the oak (Quercus Robur), elm
(Ulmus campestris), birch (Betula
alba
), and beech (Fagus sylvatica). It is of a dingy olive colour,
with a dark dorsal line, on each side of which is a row of white
spots; and it has three pairs of claspers.

The Scalloped Oak (Crocallis elinguaria)

This species is common and widely distributed, and may be seen
flying at dusk towards the end of July and throughout August. It
is represented in fig. 4 of Plate XII. The antennæ of the male are
strongly pectinated; those of the female are simple.

The caterpillar may be found in the autumn, and again in
spring, feeding on the honeysuckle (Lonicera Periclymenum),
whitethorn (Cratægus oxyacantha), blackthorn (Prunus spinosa),
beech (Fagus sylvatica), and various fruit trees. It is full grown
in June, when it turns to a chrysalis in a cocoon spun between
leaves or moss on or near the ground. It is of a greyish-brown or
greyish-purple colour, and looks very like a piece of twig.[Pg 271]

The August Thorn (Eugonia quercinaria)


Fig. 178.—The August Thorn.

Our last example of this family is the August Thorn, represented
in the accompanying woodcut. The fore wings are ochreous
yellow, crossed by two nearly parallel lines of dark brown.
In order to distinguish between this and one or two similar species
it must be observed that both these
lines are angulated near the costa,
the inner one very sharply so; and
between the two is a distinct brown
spot near the costal margin. The
hind wings are paler, and are crossed
by an indistinct darker line. The
antennæ of the male are strongly
fringed; those of the female are
simple.

The moth is very common in August and September, and is
readily attracted by lights in the evening.

The larva is grey, marbled with reddish brown. It has three
small humps on each of the sixth and seventh segments, two on
the twelfth, and one larger one on the ninth. It feeds on the oak
and various other trees during the month of June.

Family—Amphidasydæ

The seven British species of the family Amphidasydæ are
generally to be distinguished by their rather stout abdomens, and
the long shaggy hair that covers their thoraces. The antennæ of
the males are pectinated, and those of the females simple; and in
three cases the latter sex is wingless.

The caterpillars have long and slender twig-like bodies, and are
never provided with more than two pairs of claspers. The chrysalides
terminate behind in a sharp spine, and are always to be found
buried in the soil.

The Brindled Beauty (Biston hirtaria)

Early in April, and sometimes in March, this moth may be seen
in abundance, resting on the lime trees in and around our towns.
In fact, so strongly marked is its partiality to the haunts of man in
the neighbourhood of our great metropolis that it has received the
name of the Cockney. The male is represented in fig. 5 of[Pg 272]
Plate XII, and the female may be distinguished from it by her
simple antennæ and larger body.

The caterpillar is coloured with alternate bands of dark purple
brown and reddish brown. There is a yellow band on the front of
the second segment, a row of yellow spots on each side, and two
little bright yellow warts on the back of each segment. It feeds by
night on lime (Tilia vulgaris), elm (Ulmus campestris), and
various fruit trees, and often appears in such numbers that the
foliage is almost completely devoured. During the daytime it may
be seen resting on the bark, almost invariably fixed longitudinally
on the trunk, where it looks like a natural ridge of the bark which
it so closely resembles in colour. It may be found in June and
July, and in August it changes to a chrysalis at the foot of its tree,
just below the surface of the soil.

The Peppered Moth (Amphidasys betularia)


Fig. 179.—The Peppered Moth.

Although this common species displays no bright tints, yet it is
prettily marked, its whitish wings being peppered and blotched all
over with black or very dark brown. It flies in May and June,
later than any other species
of the family, and may generally
be found on fences and
tree trunks during the day.

The colour of the caterpillar
is very variable—drab,
grey, green, or brown; but
it may be known by the
deep notch in the middle of
the head, and the arrangement
of its ‘humps.’ These latter are only small reddish or whitish
projections, of which there is one on each side of the fifth, sixth,
seventh, eighth, tenth, and eleventh segments; also two on the
back of the ninth and twelfth. It feeds in August and September
on a large number of trees, including, in fact, nearly all our commonest
forest and fruit trees. In September it enters the soil to
undergo its change to the chrysalis.

Family—Boarmiidæ

In the next family—Boarmiidæ—there are about twenty British
members, most of which are very pretty moths. They differ
generally from the last family in that their bodies are more slender,[Pg 273]
and although some of them bear a resemblance to species of the
family Ennomidæ, their wings are not angulated. In several
cases the fore and hind wings are both similarly marked, a feature
very uncommon with moths.

The caterpillars of this family usually have humps on the sixth
and twelfth segments only, and have two pairs of claspers. The
pupæ are to be found either on the ground, among leaves or moss,
or beneath the soil.

The Waved Umber (Hemerophila abruptaria)

The most gaily coloured member of this family is the Waved
Umber, shown in fig. 6 of Plate XII. Like many other Geometræ,
it rests on fences and tree trunks by day with wings expanded so
that all four are displayed. It is on the wing in May and early
June, and again in August, and often frequents our gardens at
dusk.

The caterpillar is very dark brown, with a white collar on the
front of the second segment. It feeds in June and July on privet
(Ligustrum vulgare) and the cultivated rose trees of flower gardens,
and probably also on the dog rose (Rosa canina). When full
grown it spins a silken cocoon in a fork of one of the twigs, and
there undergoes its metamorphoses.

The Willow Beauty (Boarmia gemmaria)


Fig. 180.—The Willow Beauty.

Our second example of the Boarmiidæ is the Willow Beauty,
the male of which species is here illustrated. Its wings are
brownish grey, marked with dark brown lines and streaks. The
female is generally larger than the
male, and has simple antennæ. The
moth is abundant throughout England,
and may be seen generally
resting on fences and trees in June
and July.

The ground colour of the caterpillar
is much the same as that of
the moth, and is marked with a
similar darker tint. It has a yellowish
line along the spiracles, and is much like a piece of brownish
twig. It feeds on the oak (Quercus Robur), Birch (Betula alba),
ivy (Hedera Helix), and other trees, and may be found in September
and October.[Pg 274]

Family—Geometridæ

The next family contains eight moths, mostly of small size, all
of which have green wings, and are popularly known as the
‘Emeralds.’ In most cases the male may be distinguished by its
pectinated antennæ.

There is no general characteristic by which we may know all
the larvæ, but some have the head deeply notched.

The Large Emerald (Geometra papilionaria)


Fig. 181.—The Large Emerald.

This species is the largest of the family, and measures over two
inches when its wings are expanded. The colour is dull green,
with whitish bands
and spots, the arrangement
of which may
be seen in our engraving.

The moth is out
in July, and is common
in most parts
of England.

The caterpillar
feeds on birch (Betula alba), beech (Fagus sylvatica) and hazel
(Corylus avellana) in the autumn, and hybernates while still
young. In the spring it feeds again, and is full grown in June,
when it changes to a chrysalis in a cocoon spun between leaves.

The Common Emerald (Hemithea strigata)


Fig. 182.—The Common Emerald.

One of the commonest of the Emeralds is Strigata, which may
be found in June and July in all parts of England, as well as in
some localities in Scotland and Ireland.
Its wings are of a dull green colour, the
front pair being slightly scalloped on the
hind margin, and crossed by indistinct
pale lines; and the hind pair are both
scalloped and angled and crossed in the
middle by a transverse pale line. The
fringe is white, dotted with dull reddish
brown.

The caterpillar is yellowish green, except the second, third, and
fourth segments which are brownish. It feeds on oak (Quercus Robur)
and whitethorn (Cratægus oxyacantha), and may be found in June.[Pg 275]

Family—Ephyridæ

The Maiden’s Blush (Zonosoma punctaria)

The family Ephyridæ contains only six British species, chiefly
remarkable for the fact that their pupæ generally resemble those of
butterflies.

We choose for our example the pretty little Maiden’s Blush, so
called on account of the soft reddish patch on the middle of each
fore wing. It is represented in fig. 7 of Plate XII. It is moderately
common, occurring more or less in all parts of England, as
well as certain localities in the sister countries. It is a double-brooded
moth, and may be caught in May and August.

The caterpillar feeds on oak (Quercus Robur), from which it may
be obtained by beating both in June and September. It is either green
or tawny yellow, marked with yellow oblique lines on the sides.

Family—Acidaliidæ

The moths of this family, over thirty in number, are mostly of
small size, and have slender bodies. As a rule the wings are not
in the least angulated or scalloped, but in a few species the hind
pair are slightly angled on the hind margin; and both fore and hind
wings are similarly marked. The antennæ are simple in the females,
and generally only slightly ciliated in the males.

The caterpillars are long and slender, without projections, and
feed principally on low plants. The pupæ are to be found in loose
cocoons among the leaves of the food plants or under the soil.

We shall briefly notice three members of this rather extensive
family.

The Lace Border (Acidalia ornata)


Fig. 183.—The Lace Border.

The wings of this moth are silvery white, marked along the
hind margin with a beautiful lace-like border.
This border consists of delicate black and
dark grey lines, and includes, in the fore
wing, two light brown blotches, one near the
middle and the other in the anal angle. It is
abundant in England, particularly in chalky
districts, but does not seem to extend into
Scotland. It may be seen on the wing from
June to August.

The caterpillar feeds on thyme (Thymus Serpyllum) and
marjoram (Origanum vulgare).[Pg 276]

The Riband Wave (A. aversata)


Fig. 184.—The Riband Wave.

All the wings of this species are of a pale yellowish or ochreous
grey. The fore wings are crossed by three transverse dark lines,
and the hind wings by two. The space between the two outer lines
of the fore wing and that between the lines of the hind wing are
usually filled in with a greyish brown, thus forming the ‘riband’
from which the popular name of the
insect is derived; and when this is the
case the lines which border the riband
are scarcely distinguishable. Just inside
the second line of the fore wings, near
the costa, is a small but conspicuous
brown spot.

The moth flies in June and July, and
is common in all parts.

The caterpillar is dark brown except segments ten to thirteen,
which are grey. The line along the spiracles is whitish, and the
surface of the body is roughened by a number of minute warts. It
feeds on various low plants, including the meadow sweet (Spiræa
ulmaria
), water avens (Geum rivale), common avens (G. urbanum),
and knot-grass (Polygonum aviculare), during April and May.

The Blood-vein (Timandra amataria)

Our last example of the Acidaliidæ is the Blood-vein, which is
common in most parts of England in June and July.


Fig. 185.—The Blood-vein.

Its fore wings are pale grey, dusted
with darker grey, and crossed by an
oblique red streak which runs from the
tip of the fore wing to near the inner
margin of the hind wing. A slender
dark and wavy line lies outside this one,
parallel with it in the hind wing, but
meeting it near the tip of the fore wing.

The caterpillar is grey, with three white longitudinal stripes.
It feeds in the autumn on dock (Rumex), sorrel (R. acetosa), and
knot-grass (Polygonum aviculare).

Family—Caberidæ

Six species, all of rather small size, constitute the British
portion of the above family. Their wings are mostly white or pale
grey, with light markings, and without angles. The moths are[Pg 277]
to be caught with the net at dusk, or they may be seen on
fences and tree trunks during the day, with their wings fully
extended and applied closely to the surface on which they rest.

The larvæ, which have no humps, feed on trees, and change to
the chrysalis state in light silken cocoons.

The Common Wave (Cabera exanthemata)


Fig. 186.—The Common Wave.

The first of our two examples of this small family is the
Common Wave, the wings of which are pale grey, almost white,
dusted all over with small dark dots. The fore wings are crossed
by three parallel and equidistant darker
transverse lines, and the hind pair by
two. The male may be distinguished by
its ciliated antennæ.

The caterpillar is yellow or greenish
yellow, with hinder segments slightly
swollen. It feeds during the latter part
of the summer on sallows (Salix caprea
and S. cinerea) and alder (Alnus glutinosa),
and changes to a chrysalis in a light cocoon among fallen
leaves. In this state it spends the winter, the perfect insect
emerging in May or June.

This species is very abundant in most parts.

The Clouded Silver (Bapta temerata)


Fig. 187.—The Clouded Silver.

The other example is the Clouded Silver, the wings of which
are white, and clouded along the hind margin with smoky grey.
On the hind margin of the fore wings, close to the fringe, is a row
of black crescent-shaped spots; and on
the inner side of the cloudings is a waved
transverse band. In the centre of the
same wings there is a very distinct dark
spot.

This moth is not so common as the
last, but is widely distributed. It flies in
May and June.

The caterpillar is bright green on the upper side, and has a row
of orange spots, bordered with brown, down the middle of the back.
It feeds in the autumn on the blackthorn (Prunus spinosa) and
the wild cherry (P. Avium), and spends the winter in the chrysalis
state, inclosed in a light silken cocoon.[Pg 278]

Family—Macariidæ

The V Moth (Halia Vauaria)

The family Macariidæ contains only five British species, four
of which have the tip of the fore wings extended more or less into
an angle, and the hind wings are also angled to a greater or less
extent.


Fig. 188.—The V Moth.

Our only example is the V Moth, so called from the conspicuous
V-shaped blackish mark on the middle
of the costa of the fore wings. The ground
colour of all the wings is grey, with a
delicate violet tinge. There are other
dark markings in addition to the one
mentioned above, and the arrangement of
these may be seen in the woodcut.

This species is very common in all
parts, and flies at about midsummer.

The caterpillar is very variable in colour, but is generally green,
and is marked with longitudinal wavy lines. On each side is a series
of yellow blotches, forming a broken lateral stripe, and the body
is covered with minute black bristle-bearing warts. It feeds in
May on gooseberry and currant bushes, and changes to a chrysalis
in a web between the leaves.

Family—Fidoniidæ

We now come to a family of moths peculiar for their habit of
flying more or less by day. As is often the case with day-flying
moths, these are mostly prettily marked, and are consequently
often mistaken by the uninitiated for butterflies. Most of them
are to be found on heaths, downs, and open fields; but one—the
Bordered White—is met with only in fir woods.

The wings are not angulated, and the antennæ of the males are
pectinated.

The larvæ are generally to be distinguished by a couple of little
horns on one or more of the hindermost segments, and in most
cases they pupate beneath the surface of the soil.

The Common Heath (Ematurga atomaria)

Of this family we shall select two examples, the first of which is
the Common Heath, often so abundant on heaths and downs that
they are disturbed at almost every footstep.[Pg 279]


Fig. 189.—The Common Heath.

The ground colour of the wings of the male is a dull yellowish
grey, and that of the female greyish white. In both cases the
wings are crossed by irregular dark brown bands. The fringe
is barred alternately with white and dark
brown, and the whole of the ground tint
between the above-mentioned bands is
thickly dotted with dark brown. The
female is generally smaller than the male.

The caterpillar is very variable in
colour, but is generally reddish brown,
ochreous brown, or greenish, with a light
line along the spiracles, and a series of lozenge-shaped spots on the
back. It feeds on trefoils (Lotus corniculatus and L. pilosus)
and various other plants that grow on heaths.

The Bordered White (Bupalus piniaria)



Fig. 190.—The Bordered White—Male.

The male of this species is boldly marked with yellowish white
and dark brown, the arrangement of the two colours being shown
in fig. 190. The female is very different
in general appearance. Her wings
are of an almost uniform orange or
yellowish-brown tint. The fore wings
are darker near the tip, and there is
generally a darker transverse band
across the centre.

The male may often be seen flying
in the sunshine among the branches
of fir trees during May and June, but
his mate is rather less active, and is generally to be secured by
beating the branches.

The caterpillar is pale green, with whitish stripes and yellow
spiracles. It feeds during August and September on the leaves of
the Scotch fir (Pinus sylvestris).

Family—Zerenidæ

The Currant Moth (Abraxas grossulariata)


Fig. 191.—The Currant Moth.

The family Zerenidæ contains only four British moths, and of
these we select the Currant Moth or Magpie. This insect is
exceedingly common everywhere, and on account of its general
brightness of appearance, and also of its diurnal habits, it is often[Pg 280]
taken for a butterfly. The ground colour of the wings is creamy
white, with a yellow transverse band, and a yellow blotch at the
base; and the whole surface is more or less blotched with black.

From the end of June to August this moth may be seen in
abundance in our gardens,
wherever currant bushes
exist, flying about both
during the sunshine and
at dusk, with rather a
heavy movement.

The caterpillar is
white, with a yellow line
along the spiracles, and
numerous black dots.
There are, in addition to
the dots, two large black blotches on the back of each segment.
It feeds during May on currant and gooseberry bushes, also on
the blackthorn (Prunus spinosa). About the end of May it spins
a light silken cocoon, and changes to a short dumpy chrysalis of
a glossy black colour with bright yellow bands (fig. 34).

Family—Hyberniidæ

Passing over the family Ligiidæ, which contains only one
British moth, the Horse-chestnut, we come to the small but
interesting family, Hyberniidæ.

Of this we have six species, five of which favour us during the
bleakest months of the year. Two of them visit us in October and
November, and even remain with us up to Christmas. The others
follow closely on them, and may be seen from January to March.

The males have slender bodies, and their wings are full and
without angles; but the females are either perfectly or nearly
wingless. In three cases there is hardly a trace of wings in this sex,
so that they look more like spiders than moths.

The caterpillars are long and slender and without humps, and
all feed on the leaves of trees. They change to the chrysalis state
under the ground.

The Spring Usher (Hybernia leucophæaria)


Fig. 192.—The Spring Usher.

Early in February, and often even in January, this moth may be
seen in abundance in almost every oak wood, sitting on the bark of[Pg 281]
the trees, or occasionally taking a short flight in the sunshine. In
colour it is very variable. The wings have always a whitish ground
marbled and dotted with dark brown, but in some the fore wings
are almost entirely dark brown with the exception of a transverse
central bar. The female has only the
slightest rudiments of wings.

The caterpillar feeds on the young
buds and leaves of the oak (Quercus
Robur
) and sycamore (Acer Pseudoplatanus),
concealing itself among the
small leaves which it has spun together.
It is full grown in June, when it
changes to a chrysalis on the surface
of the ground, and remains here throughout the summer and part
of the following winter.

The colour of the caterpillar is very variable, but is usually pale
green with white markings.

The Mottled Umber (Hybernia defoliaria)

This very pretty moth is represented in fig. 8 of Plate XII. It
is very common in most parts, and visits us at the fall of the leaf,
generally appearing in October, and remaining on the wing till
November. Our illustration gives the usual appearance of the male,
but in some specimens the four wings are all of one uniform
reddish-brown colour, evenly dotted all over with a darker tint.
The female is quite wingless.

The caterpillar is exceedingly pretty. Its head is large and
brown. The back is brown, bordered with a fine black line. Below
this is a broad and bright yellow line, with a red spot on each
segment. The spiracles are white. It feeds during spring on oak
(Quercus Robur), whitethorn (Cratægus oxyacantha), blackthorn
(Prunus spinosa), and other trees. When disturbed it always allows
itself to fall for a foot or two, and then remains swinging at the end
of a silken fibre till danger is over, or hunger recalls it to its food.
It changes to a chrysalis on the ground about the middle of
June.

The March Moth (Anisopteryx æscularia)


Fig. 193.—The March Moth.

This is another common moth, and should be looked for during
March and April on the barks of trees in oak and other woods.[Pg 282]
The fore wings are of a dingy brown colour, paler near the base,
and crossed by a pale wavy line. The hind wings are lighter,
with a central dark spot. But this
description applies to the male only,
for the female is wingless, and may
be known by the tuft of hair that tips
the abdomen.

The caterpillar is pale green,
clouded with a darker tint, and has
a white line on each side of the back.
It feeds in May on the three trees named for the last species, also
on lime (Tilia vulgaris) and elm (Ulmus campestris).

Family—Larentiidæ

This is by far the most extensive family of the Geometræ,
containing as it does considerably over a hundred species, or well
nigh a half of the whole group.

The wings of the various species are smooth and more or
less glossy, and the front pair are generally crossed by several
wavy lines. Many of the moths, and particularly those known
popularly as the Pugs, are very small. Representatives of the
family are to be met with almost throughout the year—from early
spring to the middle of the winter.

Most of the caterpillars are rather long and slender, and without
humps; and green is the prevailing colour. They feed either on trees
or low plants, often protecting themselves in folded leaves; and some
of the smaller species show a decided preference for flowers and seeds.

We shall select about a dozen of the commonest members for
individual description.

The November Moth (Oporabia dilutata)


Fig. 194.—The November Moth.

Our first example is the November
moth—a rather dingy and very variable
species that may be found almost
everywhere in October and November.
The ground colour of the fore wings is
dingy grey, crossed by several darker
lines, subject to considerable variations.
The hind wings are paler, with two slender darker lines
parallel with the hind margin.[Pg 283]

The caterpillar feeds on many trees, the principal of which are
the oak, whitethorn and blackthorn. Like the perfect insect, it is
very variable in colour, but is generally of a bright green, with
reddish or purplish spots on the back and sides. The spiracles are
yellow or orange, and below them is a white stripe. It is full fed
in June.

The Twin-spot Carpet (Larentia didymata)


Fig. 195.—The Twin-spot Carpet.

The Twin-spot Carpet is common throughout Great Britain,
and the beginner is likely to meet with it in June and July
during his first season. Our illustration represents
the male, the fore wings of which
are greyish brown, crossed by several dark
lines, and with a double dark and conspicuous
spot near the middle of the hind margin.
The female is much lighter, and the markings
are also lighter and less distinct.

The caterpillar is pale green, with a narrow
whitish line along the spiracles. It feeds in April and May on
the leaves of the wood anemone (Anemone nemorosa), chervil
(Chærophyllum temulum), and other plants.

The Grass Rivulet (Emmelesia albulata)

We represent the genus Emmelesia by the Grass Rivulet—a
pretty little moth that flies in June, and which is widely distributed
though not abundant.


Fig. 196.—The Grass Rivulet.

Its fore wings are pale grey, crossed by
several white lines, the arrangement of which
may be seen in our engraving. The hind
wings are of the same ground colour, but have
no markings except a white wavy line near
the hind margin.

The caterpillar feeds during July and
August on the seeds of the yellow rattle (Rhinanthus Crista-galli),
protecting itself from its enemies by spinning together the petals
of the flowers; and when full grown it changes to a chrysalis under
the same cover.

The Netted Pug (Eupithecia venosata)

We now come to the enormous genus Eupithecia, containing
about fifty small species, most of which are known as ‘Pugs.’[Pg 284]
Many of these are only imperfectly known, there being yet much
to learn about their earlier stages.


Fig. 197.—The Netted Pug.

The Netted Pug flies in May and June,
and is to be found in most parts of Great
Britain. Its fore wings are brownish grey,
crossed by two zigzag light bands, both of
which are bordered with black, and divided
throughout by a fine dark line. There are
also other dark lines, both transverse and
longitudinal, arranged as here represented.

The caterpillar feeds during July inside the seed capsules of
campions (Silene Cucubalis, S. maritima, S. acaulis, and Lychnis
diurna
) and catchfly (Silene gallica and S. nutans).

The Narrow-winged Pug (Eupithecia nanata)

Early in May, and frequently in April, this pretty little moth
may be seen flying about at dusk among the
heather on our moors. It is one of the first
Pugs of the season, and is widely distributed,
and very common in some localities.


Fig. 198.—The Narrow-winged Pug.

Its wings are dark grey, and marked with
several transverse wavy light lines. The fringe
is dark grey, spotted with white.

The caterpillar feeds during August and
September on the ling (Calluna vulgaris) and heath (Erica cinerea
and E. Tetralix).

The Brindled Pug (Eupithecia abbreviata)

Our last example of the Pugs is the Brindled Pug, another
early species, appearing on the wing in March and April. It is
common in most parts, and may generally be
easily obtained by searching fences and tree
trunks.


Fig. 199.—The Brindled Pug.

Its fore wings are very long in proportion.
The colour is yellowish brown, crossed by darker
lines. The fore wings have a very broad band
of the ground colour, broken by two short lines,
and crossed by a slender angulated stripe.

The caterpillar feeds on the oak in June.[Pg 285]

The Small Seraphim (Lobophora sexalisata)

This moth is very much like the Pugs in general appearance,
and is quite as small and even smaller than some of them; but it
and the other members of its genus differ from
the Pugs in that they cover their hind wings
when at rest.


Fig. 200.—The Small Seraphim.

The fore wings are yellowish or pale brownish
grey with four paler transverse lines, the two
median ones of which are divided throughout
by a darker fine wavy line. The hind wings
are grey, paler at the base, and crossed centrally
by a double darker line. This species flies in May and June,
and though apparently widely distributed, can hardly be described
as common.

The caterpillar feeds on the white willow (Salix alba) and
sallow (S. caprea) in August and September; and the chrysalis
may be found in a silken cocoon among the fallen leaves throughout
the winter.

The Blue-bordered Carpet (Melanthia bicolorata)

This same family (Larentiidæ) is remarkable for its large
number of pretty moths, popularly known as the ‘Carpets,’ many
of which are exceedingly common in our woods
and gardens.


Fig. 201.—The Blue-bordered Carpet.

Our first example of these is the Blue-bordered,
which is pretty well represented in
several counties of Great Britain and Ireland.
Its white fore wings are boldly marked with a
blotch of greyish brown at the base, and another
extending from the middle of the costal
margin more than halfway across. The hind
margin is marked with two bluish grey bars, separated by a white
line. The hind wings are white, with a very small dark spot, and
a bluish grey margin something like that of the fore wings.

The caterpillar is green, with longitudinal stripes of a darker
and lighter shade. It feeds in June on the alder (Alnus glutinosa)
and blackthorn (Prunus spinosa); and when full grown it changes
to a brown chrysalis within a light silken web.

The moth flies in July and August.[Pg 286]

The Beautiful Carpet (Melanthia albicillata)


Fig. 202.—The Beautiful Carpet.

The Beautiful Carpet belongs to the same genus as Bicolorata.
Its wings are of a rich creamy white, clouded with grey along the
hind margin. The basal blotches of the
fore wings are large, of a dark brown
colour, and marbled with a light tint.
Near the tips of these wings is another
conspicuous blotch of the same colour,
from which a delicate wavy dark line runs
to the inner margin. A small dark spot
also lies near the middle of the costal
margin of each of the four wings.

The caterpillar is green, with a white
line along the spiracles, and a triangular reddish spot on the back
of segments four to ten inclusive. It feeds on the bramble (Rubus
fruticosus
), raspberry (R. Idæus), and wild strawberry (Fragaria
vesca
). It may be found in June and July.

The moth flies in June.

The Common Carpet (Melanippe sociata)


Fig. 203.—The Common Carpet.

The genus Melanippe contains twelve species, some of which
are extremely common. One of these moths—the Common Carpet—is
represented in fig. 203. Its wings are
all of a smoky-brown colour, crossed by
numerous white lines, the arrangement of
which may be gathered from our illustration
better than from a written description. It
is a double-brooded insect, appearing first in
May, and then again about the end of July.

The caterpillar is mottled with shades of
brown and grey. On the back are five or six
greyish-white lozenge-shaped marks, and there are a few white dots
on the back of each segment. It feeds on the hedge bedstraw
(Galium Mollugo), and when full grown it changes to a chrysalis
in a light cocoon on the ground.

The Silver Ground Carpet (Melanippe montanata)


Fig. 204.—The Silver Ground Carpet.

In this species the ground colour is silvery white. The bases of
the fore wings are blotched with pale brown, and a dark brownish-grey[Pg 287]
bar, containing a black spot, crosses the middle. The hind
margins of the fore wings are faintly marked with pale brown,
and lines of the same tint, more or less distinct, cross the hind
wings.

This moth is very common in all
parts of the country, and may be seen
on the wing throughout the summer.

The caterpillar is light brown, with
several longitudinal lines of different
colours. On the back of each of the
segments seven, eight, and nine is a
distinct black V-shaped mark, terminating
behind with a bright red spot. It feeds on the primrose
(Primula acaulis) in the autumn, hybernates through the winter,
and is full grown about the beginning of April.

The Garden Carpet (Melanippe fluctuata)

Our third and last member of this genus is the Garden Carpet—a
moth that must be pretty well known to almost everybody, since
it is the commonest of all the Geometræ that frequent our gardens.


Fig. 205.—The Garden Carpet.

The fore wings are pale grey or brownish,
with a patch of dark greyish brown
at the base, another larger one on the
middle of the costa, and a third near the
tip. The wing is usually clouded between
the middle blotch and the inner margin,
and numerous fine wavy lines, more or
less distinct, cross the wing.

This moth may be seen throughout
the summer, from May to September, but is most abundant in
June and July.

The caterpillar is extremely variable in colour, being either
green, brown, or grey, or some intermediate tint; and is marbled
and dotted with dark brown on the back. It feeds on the nasturtium
(Tropæolum majus), rape (Brassica Napus), and various
other cruciferous plants; and may be found from April to August.

The Yellow Shell (Camptogramma bilineata)

Passing over two smaller genera, we come to the beautiful
little Yellow Shell. This moth is so abundant in most parts[Pg 288]
that we arouse it at almost every stroke while beating low
bushes.


Fig. 206.—The Yellow Shell.

All its wings are yellow, and crossed by numerous delicate
white and brown lines. The most conspicuous
feature is the two white lines,
with dark brown edging, crossing the fore
wings.

The caterpillar feeds by night, and is
therefore seldom seen except by those who
make special nocturnal searches with the
aid of a lantern or sweep net. It devours
various grasses, and hides itself among the
roots or under stones during the daytime. It is full grown in April
or May. The colour is dull pale green, with a dark green dorsal
line, and two white stripes on each side.

The Small Phœnix (Cidaria silaceata)

Again passing over a few small and less important genera, we
select the small Phœnix as the last example of this very extensive
family.


Fig. 207.—The Small Phœnix.

The fore wings of this species are dark brown, paler toward the
hind margin. Most of the wing rays are
generally of a pale yellowish colour, and a
variable and complicated system of whitish
lines crosses the wings near the base, and
another near the hind margin. Among the
latter there is always a series of dark
triangular spots, with apices pointing towards
the hind margin.

This moth is moderately common throughout the British Isles,
and is double brooded, appearing in May and August.

The caterpillar is green, with a row of brown spots along the
middle of the back. When full grown it changes to a chrysalis in
a light web.

Family—Euboliidæ

This is the last family of the Geometræ we shall notice, and
contains ten species. Most of these are rather pretty moths, and
all have the tips of the fore wings more or less pointed. As a rule,
too, there is a dark streak running from the very tip of the wing for
a short distance obliquely inward.[Pg 289]

They are generally very light sleepers, and are easily beaten
from their hiding places during the day.

The larvæ are not humped, and may be found feeding on low
plants.

We shall briefly examine two species.

The Small Mallow (Eubolia limitata)

This moth is pretty abundant in waste places from June to
August, and is easily obtained by
lightly beating the foliage of small
bushes and low plants.


Fig. 208.—The Small Mallow.

Its fore wings are pale brown
crossed by a broad central bar, the
edges of which are darker. The hind
wings are of a paler brown, and are
crossed by two or three fine wavy lines.

Although the perfect insect is so
common, the caterpillar seems to be
seldom met with. It is a grass feeder, and may be looked for in
May and June.

The Treble Bar (Anaitis plagiata)

Our last example of the Geometræ is the Treble Bar, a very
pretty moth, which is illustrated in fig. 9 of Plate XII. It may be
readily identified by the aid of this coloured picture, and therefore
need not be described in words. It is pretty generally distributed
throughout the British Isles, and is in some parts a very abundant
species, particularly so in the neighbourhood of London.

The caterpillar is brown, with paler spaces between the segments.
The dorsal line is black and interrupted, and a yellow line runs
along each side. It feeds on the leaves and flowers of the
perforated St. John’s wort (Hypericum perforatum).

This insect is double brooded, the moth appearing in May and
August, and remaining with us throughout the month following in
each case.[Pg 290]


CHAPTER XXI

THE MICRO-LEPIDOPTERA

The butterflies, and all the moths contained in the groups of the
last four chapters, are commonly spoken of as constituting the
Macro-lepidoptera; but in addition to these there are many hundreds
of small British moths that represent what is known as the
Micro-lepidoptera.

It is not usual for young entomologists to have much to do with
the ‘Micros’ until they have had a little practical experience with
the larger species; in fact, a good number of them never seem to
extend their knowledge beyond the limits of the ‘Macros’ except that
they may make an occasional capture of a Micro that happens to fly
across their path.

Now, since it would be practically impossible to deal fairly, even
in outline, with both these divisions of the Lepidoptera in a work
of the present dimensions, I have devoted most space to the larger
species so as to meet the probable requirements of the majority of
my readers. But in order that the beginner may also have the
means of introducing himself intelligently to a study of the ‘Micros,’
I shall set apart this chapter for a simple account of the broad
principles of their classification, illustrated by means of a few
types, so that the collector may at least know something of the
insects he captures, even though he may not be able at once to fix
on their names.

The young entomologist, thus provided with the broad features
that enable him to roughly classify the specimens which reach his
cabinet, may, as his store increases, pay an occasional visit to a
public museum or the private collection of an entomological friend,
and so obtain the names and other details he may require.

The Micro-lepidoptera are divided into five main groups—Pyralides,
Pterophori, Crambi, Tortrices, and Tineæ, each of[Pg 291]
which is divided into families and genera, as we have seen in the
case of the ‘Macros.’

Pyralides

The Pyralides may be easily distinguished by the proportionately
long fore wings, long legs, and elongated abdomen. Some of
them have wings of a pearly lustre, and are accordingly known
popularly as the ‘Pearls.’ Some species fly in bright sunshine,
others appear on the wing before sunset, and fly till dusk; others,
again, are purely nocturnal in their habits. All, however, are
apparently light sleepers, and may be easily beaten out of their
resting places and netted by day. Some of these moths are
common everywhere, but the majority of them are very local,
though they may be extremely abundant where they occur.

The larvæ have a glossy and bristly appearance, and are
generally gregarious in their habits.

This group contains about eighty species, arranged in five
families as follows:

  1. Pyralididæ, including about forty species.
  2. Botydæ, about thirty species.
  3. Steniiadæ, containing only five species.
  4. Hydrocampidæ, four species.
  5. Acentropodidæ, containing only one.

The Tabby (Aglossa pinguinalis)

The first of these families contains the Tabby or Grease Moth,
commonly met with both in the larval and perfect states in barns
and stables.


Fig. 209.—The Tabby or Grease Moth.

Its fore wings are brownish grey,
crossed with zigzag darker lines, and
having a black spot near the centre of
the costal margin. The term ‘Tabby’
has been applied on account of the
fancied resemblance of the transverse
markings to the fur of a tabby cat,
and the other popular name was given
under the belief that the caterpillar feeds on fatty matter, but it is
extremely doubtful whether this supposition is correct.

The caterpillar probably feeds exclusively on the vegetable
accumulations that lie in the undisturbed corners and crevices of[Pg 292]
outhouses and stables, and lives concealed in silken tubes, strengthened
outside by fragments of hay, chaff &c. that have been spun
together. It feeds from September to April, except during very
severe weather, and when full grown it leaves its tube, and changes
to a chrysalis in a light silken cocoon in some secluded corner.

The moth emerges in July.

The Meal Moth (Pyralis farinalis)

The same family contains the common Meal Moth, so called
because in the larval state it feeds on meal and allied substances.


Fig. 210.—The Meal Moth.

The fore wings are yellowish grey, with
reddish basal patches, a broad reddish band
along the hind margin, and two whitish indented
transverse lines. The hind wings are
grey, and are crossed by two lines similar to
and continuous with those of the front pair.

This moth is to be found in abundance
throughout the summer months in places
where corn, meal, and grain are stored in large quantities, sitting
on walls and rafters during the daytime, and taking to flight in
the evening.

The caterpillar feeds on corn, meal, grain, bran, &c., and lives
concealed in a silken tube covered outside with particles of its food
substance. It is not fully grown till nearly two years old, and
then changes to a chrysalis in a white silken cocoon.

The Small Magpie (Eurrhypara urticata)


Fig. 211.—The Small Magpie.

The family Botydæ contains the moths that are popularly
known as the ‘Pearls’ on account of the pearly lustre of the wings.
One of its species—the Small Magpie—is
shown in the accompanying illustration.
Its fore wings are pearly white, with
blackish hind margin, a yellow streak at
the base, and blackish markings, the arrangement
of which may be seen in the
figure.

It is a very common moth, flying at
dusk during June and July in waste places
where the stinging nettle grows.

The caterpillar is whitish, with a dark dorsal line. It feeds on the[Pg 293]
stinging nettle (Urtica dioica), always remaining concealed between
leaves which it has spun together with silken threads.

The Mother-of-Pearl (Botys ruralis)

This is another very common species of the family Botydæ,
abundant almost everywhere, and to
be found on the wing from June to
August.


Fig. 212.—The Mother-of-Pearl.

Its wings are whitish, and exhibit
a very decided pearly lustre, and all
the markings are of a dull dark grey.

The caterpillar is glossy, and has
a semi-transparent appearance. It is
greenish white above, with a darker
line down the back; and the sides are
of a brighter green. It feeds on the stinging nettle (Urtica dioica)
during May.

The Garden Pebble (Pionea forficalis)

The same family contains also the Garden Pebble, which is one
of the commonest frequenters of gardens, both in town and
country.


Fig. 213.—The Garden Pebble.

The fore wings are pale yellowish grey with brown markings.
The latter include a fine line from the tip to
the middle of the inner margin, and another
paler one inside and parallel with this, having
a dark spot near its centre. The hind
wings are lighter, and have a pale and interrupted
line parallel with the hind margin.

The caterpillar is pale greenish, with a
dark line along the back and on each side.
It feeds on the cabbage and other cruciferous plants.

The moth flies from May to the end of the summer, and the
caterpillar may be found about midsummer, and again in the
autumn.

The Beautiful China Mark (Hydrocampa stagnata)


Fig. 214.—The Beautiful China Mark.

Our last example of the Pyralides—the Beautiful China Mark—belongs
to the family Hydrocampidæ. This small family is[Pg 294]
remarkable for the fact that its four species spend their larval state
in the water, feeding on the under surfaces of the leaves of water
lilies and other aquatic plants. These curious
larvæ live either in cases which they construct
for their protection, something after the fashion
of the larvæ of caddis flies, or quite free in the
water, and then they are supplied with special
breathing organs that enable them to absorb the
oxygen held in solution in the water.

The moth we have selected for illustration
is a very common species, and may be seen flying in great numbers
in the neighbourhood of ponds during June and July.

The Pterophori

The members of this remarkable group are easily distinguishable
from all other moths by the feathery appearance of their wings, a
feature that has gained for them the popular name of Plume Moths.
Their fore wings are more or less divided or cleft, and their hind
wings are generally divided into three distinct feathery plumes.

The larvæ are hairy, and when full fed they suspend themselves
by their anal claspers, and change to the chrysalis state without
any kind of covering. They are generally to be found in spring
and early summer, but some of them feed in the autumn.

The chrysalides are often hairy, though some of them are
perfectly smooth.

Plume moths are to be met with more or less throughout the
year. Many of the earlier species appear on the wing in spring
and early summer; but the late feeders emerge in the autumn, and
hybernate through the winter, often taking to the wing on the mild
days of our coldest months.

The Pterophori include only about forty British species, all of
which, with two exceptions, belong to the family Pterophoridæ. The
two exceptions represent as many families—one the Chrysocorididæ,
and the other the Alucitidæ.

Platyptilia gonodactyla

This is one of the commonest of the Pterophoridæ, generally
appearing in our gardens and in waste places towards the end of
May, and continuing with us for some time. It starts from its
retreat at or before sunset, and remains on the wing after dark.[Pg 295]


Fig. 215.—Gonodactyla.

Its fore wings are ochreous grey, with a narrow brown costal
margin, and a triangular brown patch on the costa. Beyond this
patch the wing is cleft. The hind wings consist
of three distinct brownish plumes, the
third of which has a small tuft of black
scales projecting from the middle of the
inner margin.

The caterpillar feeds on the flower stalks
of the coltsfoot during March and April.

Leioptilus osteodactylus

This is another species of the same family.
It is not uncommon, but is more local than
the last.


Fig. 216.—Osteodactylus.

Its fore wings are pale yellow, with a
small brown dot at the commencement of
the dividing fissure, and a brown blotch on
the costal margin nearer the tip. The hind
wings are divided into three distinct plumes
like those of Gonodactyla.

This is a later species, appearing on the
wing in July.

Aciptilia pentadactyla


Fig. 217.—Pentadactyla.

The fore wings of this species are white,
frequently with a few greyish scales, and are
deeply divided into two feathery plumes.
The hind wings are pure white, and consist
of three plumes.

This pretty insect is common and widely distributed, and flies
during June and July.

The caterpillar feeds on the convolvulus in May.

Alucita hexadactyla

Our last example of the Pterophori is the Twelve-plume Moth,
the only British representative of the family Alucitidæ.


Fig. 218.—Hexadactyla—Enlarged.

This little insect is of a yellowish colour, with two dark bands
across the fore wings; and both fore and hind wings are divided
into six distinct feathers. It is a common moth, and frequents[Pg 296]
sheltered spots, flying at dusk. It appears in August, remains on
the wing till October, and then hybernates till the following April.
During the winter it is commonly met with
in outhouses and even in dwelling houses.

The caterpillar feeds during June and July
on the flower buds of the honeysuckle (Lonicera
Periclymenum
). It is not hairy, like
most of the larvæ of the last family; and,
unlike these, it changes to a chrysalis in a
silken cocoon.

Crambi

The third group of the ‘Micros’ is the Crambi, and contains
about eighty species, arranged in four families.

Some of them are common moths with which all must be more
or less familiar, as they are roused from the grasses on which they
repose at almost every footstep as we walk through meadows in the
summer. When at rest, they present a very peculiar appearance.
Their wings are wrapped closely round their bodies in such a manner
that they are hardly distinguishable from the stems on which
they repose.

The larvæ have sixteen limbs, and are very variable in their
habits. Some feed among moss or dry stems in silken tubes, some
on the stems of reeds, and others inhabit the hives of bees and feed
on the wax of the honeycomb.

The four families are:

  • 1. Chilidæ—five species.
  • 2. Crambidæ—about thirty species.
  • 3. Phycidæ—over forty species.
  • 4. Galleridæ—five species.

Chilo Phragmitellus

This species is one of those moths known as the ‘Veneers,’ and
is popularly termed the Wainscot Veneer. It is one of the largest
of the family Chilidæ.


Fig. 219.—Phragmitellus—Enlarged one-half.

Its fore wings are long, narrow, and pointed at the tip. They
are of a pale ochreous brown colour, with a row of small black dots
along the hind margin.

The caterpillar is pale grey, with brown stripes; and the head[Pg 297]
and second segment are yellowish brown. It feeds on the common
reed (Phragmites) in the autumn, and hybernates till the following
spring, when it resumes its
feeding.

This insect is rather local,
but may be searched for in all
marshy places where reeds
abound.

Crambus hamellus


Fig. 220.—Hamellus—Slightly enlarged.

The family Crambidæ is represented
by the above-named
species, which has the popular title of
Pearl-streak Veneer. It is not a common
moth, but is to be obtained in some localities
by beating low herbage.

Its fore wings are ochreous and glossy,
with a silvery streak from the base, running
almost parallel with the costal margin. The
hind margin is yellow, bordered inside by a
wavy brown line. The hind wings are pale greyish brown with a
yellowish margin.

Crambus tristellus

The same family contains the species Tristellus, which, unlike
the preceding insect, is abundant everywhere.


Fig. 221.—Tristellus.

Its fore wings are generally yellowish
brown, but exceedingly variable. A pale
streak runs from the base to just beyond
the middle of the wing, and is then forked.
Near the hind margin is a very indistinct
brown wavy line. The hind wings are
dull smoke colour with a light fringe. As
with the other moths of the family, its labial palpi are very long.

The moth flies from July to September.

Crambus hortuellus

This is also an abundant species, to be met with everywhere
during June and July.


Fig. 222.—Hortuellus.

Its fore wings are dull ochreous brown. The wing rays are[Pg 298]
whitish near the inner margin, and a brown line with a silvery
edging crosses near the hind margin. The hind wings are dull
smoky brown, with a shining surface, and the
fringe is light.

The larva is pale grey with dark grey spots,
and may be found among moss in April and
May.

Galleria mellonella

Our last example of the Crambi is a moth
that the young entomologist is not likely to meet with unless he
happens to be in the neighbourhood of one of its haunts, but its
habits are so peculiar that we are
tempted to introduce it on that account.


Fig. 223.—Mellonella.

It belongs to the family Galleridæ,
the larvæ of which feed on the wax
combs in the hives of bees and in the
nests of wild bees. They are protected
from the stings of the inmates by silken
tubes which they construct, and by the hardened covering of their
heads and front segments—the only parts that remain exposed while
they are feeding.

The fore wings of the moth are reddish-grey or brownish,
sometimes with a greenish tinge, and yellowish along the inner
margin. The hind wings are greyish brown.

It flies in July and August, and the caterpillar feeds in May and
June.

The Tortrices

This is a large group of moths, deriving their name from the
peculiar habit of a number of the larvæ of twisting or rolling up
leaves for their protection. This habit, however, is not common to
all, for some feed on stems and flowers, and others devour seeds and
fruits.

The perfect insects may easily be known by the shape of the
wings. The fore pair are gracefully curved on the costal margin in
such a way that, when the insect is at rest with its wings closed, its
outline is much the shape of a bell.

The identification of the various species of this extensive group
is no easy task, for many of them are so variable in their colouring
that insects of the same species are often very different from each[Pg 299]
other. So puzzling indeed is this tendency to run into varieties
that many insects, once considered to belong to separate species,
have been reduced to one; and this has been the case in a number
of instances.

There are so many of these little moths that we cannot even
give a representative of each family, but the following outline will
serve to show the extensiveness of the group.

  • Family 1. Tortricidæ, about sixty species.
  •  ”  2. Penthinidæ, ” twenty ”
  •  ”  3. Spilonotidæ, ” twelve ”
  •  ”  4. Sericoridæ,  ” twenty-seven species.
  •  ”  5. Sciaphilidæ, ” twenty-four  ”
  •  ”  6. Grapholithidæ, about one hundred and fifty species.
  •  ”  7. Pyraloididæ, four species.
  •  ”  8. Conchylidæ, about fifty species.
  •  ”  9. Apheliidæ, three species.

We shall now briefly examine a few of the commonest insects of
the group.

Tortrix xylosteana

This pretty moth is common in most parts, and may often be
met with in abundance in wooded localities during July. It belongs
to the family Tortricidæ.


Fig. 224.—Xylosteana with wings closed.

Its fore wings are ochreous brown. A very dark
oblique streak, edged with yellow, runs from the
inner margin of the base. A reddish patch in the
centre of the wing, also edged with yellow, is narrow
on the costa, and expands as it approaches the inner
margin. Beyond this are another dark patch on the
costa and two reddish-brown blotches on the hind
margin.

The larva is greenish brown, marked with white
spots which have black centres; and it feeds on oak (Quercus
Robur
), honeysuckle (Lonicera Periclymenum), and other plants,
in the month of May.

Tortrix viridana


Fig. 225.—Viridana.

In June and July this pretty but destructive little insect may be
seen flying in abundance in almost every oak wood. Its fore wings
are one uniform pale green with the exception of a streak of yellow[Pg 300]
along the costal margin; and, when at rest, scores may exist on a
single twig without being seen unless closely examined. The hind
wings are of a pale smoky tint, and rather glossy.

The larva is green, with black spots, and
feeds in May and June on the oak and other
trees, often almost completely devouring the
foliage.

Peronea cristana


Fig. 226.—Cristana—Enlarged.

This moth is not so generally abundant, but is very common in
many of the woods of the south.
It is remarkable for the large number
of varieties that have been observed,
many of which have been regarded
as distinct species.

Its fore wings are of some shade
of brown or grey, with a light streak
of variable colour along the inner
margin, and a tuft of raised white
scales in the middle of the wing.

It flies during August and September.

Ptycholoma lecheana

Our last example of the family Tortricidæ is Lecheana, a moth
that is common in most parts in June and July.


Fig. 227.—Lecheana.

Its fore wings are brown, lighter towards the
base. There are no very distinct markings, but
there is generally a darker patch in the middle of
the wing, edged with a silvery streak on each side.

The larva feeds on several trees, including oaks
and elms, in the month of May.

Penthina pruniana


Fig. 228.—Pruniana.

The next family—Penthinidæ—contains the
common species Pruniana, which may be readily
known by its boldly marked wings. The basal
portion of the fore wings, to the extent of nearly
two-thirds of the whole, is very dark brown. The remaining third
is almost white, and clouded with grey. The hind wings are smoky
brown with a paler fringe.[Pg 301]

The caterpillar of this species feeds on the blackthorn (Prunus
spinosa
) in May, and the moth flies in June and July.

Antithesia salicella

This moth is not nearly so common as the last species, but is
fairly plentiful in some localities in the south of England. It
belongs to the same family as Pruniana.


Fig. 229.—Salicella.

The fore wings are whitish at the base
and along the inner margin, but the light tint
is dotted and clouded with shades of brown.
The remainder of the wings is marbled with
dark brown of different depths, relieved near
the hind margin with a little blue. The hind
wings, as is usual with the Tortrices, are dull
smoky brown.

The caterpillar is reddish brown with black spots, and feeds
during May in rolled leaves of willows.

The moth flies in August and September.

Sciaphila octomaculana

Our single example of the family Sciaphilidæ is the species
Octomaculana, which, though not
very abundant, is widely distributed,
and moderately common in
parts.


Fig. 230.—Octomaculana—Enlarged.

Its fore wings are white, dusted
with grey, and each is marked with
four dark grey patches which have
given rise to its specific name—a
word which signifies ‘eight-spotted.’
The hind wings are grey.

The caterpillar feeds on thistles and other plants, and the
moth flies from August to October.

Ephippiphora cirsiana

This insect represents the family Grapholithidæ. It is a
common moth, and is widely distributed.


Fig. 231.—Cirsiana—Enlarged.

Its fore wings are greyish brown, with a large white patch on
the middle of the inner margin; and beyond this white, in the[Pg 302]
anal angle, is a pale grey patch containing three or four black
dots. The tips of the wings are reddish brown.

The moth flies in June and July;
and the larva, which feeds on thistles,
may be found in the stems from October
to the following May.

Carpocapsa pomonella


Fig. 232.—Pomonella.

The same extensive family contains
a few moths that are very destructive to
our fruits, the larvæ burrowing into and
living entirely within their substance.
One of these—Pomonella—is
popularly known as the Codlin, as
its larva is so often found in the
interior of small apples of the
same name.

The fore wings of this insect
are grey, with a number of dark
transverse lines. The spot in the
anal angle is edged with a coppery
tint, and inclosed by a curved
black line.

This moth is common in all
parts, flying during June and July; and the larva may be looked
for in apples and pears in August and September.

Xanthosetia zoegana


Fig. 233.—Zoegana—Enlarged.

Our last example of the Tortrices is Zoegana, which belongs to
the family Conchylidæ. Its fore
wings are yellow, with a reddish
streak along the costa near the base,
and a small reddish spot opposite this
near the inner margin. The tip of
the wings is dark reddish brown, in
the middle of which is a large yellow
spot.

This moth is widely distributed,
and in some parts common. It flies
from May to August, and the larva feeds on the small scabious
(Scabiosa columbaria).[Pg 303]

The Tineæ

We have noticed that the Tortrices form a very extensive group
of moths, but they are far outnumbered by the Tineæ, for of these
there are over seven hundred known British species.

Of course, among so many species we are sure to find considerable
variety in form and structure; but notwithstanding this, the
Tineæ form a well-marked division, and the beginner will find but
little difficulty in distinguishing between these and the other
Micros.

The wings are long and narrow, and are remarkable for the
length of the fringe, particularly that of the hind wings. The bodies,
too, are long and slender.

The larvæ are exceedingly variable. Some have the usual
number of sixteen limbs, and others have as many as eighteen.
Again, the larvæ of several genera have only fourteen legs, and
some are absolutely legless.

With regard to their food and habits, they are equally variable,
for while some feed exposed, others are always protected in rolled
leaves. Some construct for themselves portable tubes, so that they
always remain under cover, and are at the same time perfectly free
to ramble in search for food. Some, also, are leaf miners; and the
group includes the so-called ‘Clothes Moths,’ whose larvæ devour
our garments, furs, and the upholstering of our furniture.

We shall now briefly notice a few species, in order that we may
become better acquainted with the general characters of the group.

Diurnea fagella

This moth represents the small family Epigraphiidæ, containing
only six species, all of which appear in the winter or
early spring.


Fig. 234.—Fagella.

The present species is very common in
most parts, and may be seen at rest on the
barks of trees in March and April.

The fore wings are usually pale grey or
yellowish grey, and dotted with brown;
but there is a great variety both in the
depth of the ground colour and the distinctness
of the markings. Our illustration gives the usual
appearance of the insect.[Pg 304]

The caterpillar feeds on various trees in September and October,
always protected between leaves that it has spun together.

Adela cuprella


Fig. 235.—Cuprella.

The family Adelidæ contains ten species, all remarkable
for the great length of their antennæ. The
one selected for illustration is a beautiful little moth
with bright bronzy green fore wings, tinged with a
rich glossy violet. The hind wings are brown with a
glossy surface.

This moth does not seem to be widely distributed,
but is fairly plentiful where it occurs. Wimbledon
Common and Epping Forest are good localities for it.
It is on the wing in April and May.

Hyponomeuta Padellus

The family Hyponomeutidæ contains about twenty insects,
some of which are very common and exceedingly destructive to
our trees. In May and June hawthorn and
fruit trees may be seen swarming with the
gregarious larvæ of some of them, and almost
entirely stripped of their leaves.


Fig. 236.—Padellus.

The species here figured has grey or white
fore wings with three rows of black dots. The
hind wings are darker grey without dots.

The larva feeds on hawthorn, apple, and other trees. The perfect
insect flies in July and August.

Depressaria nervosa


Fig. 237.—Nervosa—Twice Natural Size.

The next family—Gelechiidæ—is
represented by the species
Nervosa, which is common in
many localities.

Its fore wings are reddish
brown, and are marked by a
number of short longitudinal
streaks of a darker colour. The
hind wings are light grey.

The caterpillar is black, marked with black spots in white rings,
and having yellow side stripes. It feeds on the flowers of the[Pg 305]
hemlock water dropwort (Œnanthe crocata) during June and
July.

The moth flies in August and September.

Harpella Geoffrella


Fig. 238.—Geoffrella.

The same extensive family contains the moth Geoffrella, represented
in the accompanying cut. This is an exceedingly pretty
insect. The basal portion of its fore wings is
yellow, with two longitudinal dark streaks, the
outer one of which is bent towards the inner
margin near the middle of the wing. The remaining
portion of the wings is brown, with two
yellowish triangular spots, one on the costal and
one on the inner margin. On the middle of the
costa is a short dark streak.

This moth appears in May and June, and is rather local, but very
abundant in some parts.

Coleophora ibipennella



Fig. 239.—Ibipennella—Enlarged.

The family Coleophoridæ contains about seventy small moths,
characterised by their very narrow and pointed wings, with long
fringes, and also, generally, by a little tuft of hair on the first joint
of the antennæ.

The larvæ live in little cases which they construct, and feed on
various leaves and seeds. They spend the winter within their
cases, and change to the chrysalis state in spring or early summer.[Pg 306]

One of these moths—Ibipennella—is shown in fig. 239. Its fore
wings are white, with a satiny gloss, and brownish towards the
tips. The ‘nervures’ are generally of a yellowish tinge. The
hind wings are dark grey.

The larva feeds on the birch (Betula alba), and may be seen
walking on the surface of the leaves, carrying, or rather dragging
after it, the pistol-shaped case in which it lives, nothing protruding
save its head and front legs. It is full fed in May, and the moth
flies in July.

Tischeria complanella


Fig. 240.—Complanella—Enlarged.

This species represents the rather extensive family Elachistidæ,
the members of which have narrow and pointed wings. Many of
them are adorned with beautiful metallic tints, but are generally
so small that a lens is
necessary to show up
the splendour of their
clothing. Most of the
larvæ are leaf miners,
and are easily reared.
All that is necessary is
to pluck a few twigs,
the leaves of which,
when held up to the
light, reveal the tiny
larvæ in their burrows,
and place them in a vessel of water. They do not feed long, and
it is probable that most of the larvæ so treated will be ready to
change before the leaves have become dry. The present species
has bright yellow fore wings, with pale grey cloudings at the hind
margins. It is very abundant in many parts, and flies during the
month of June.

The larva is one of the numerous leaf miners, and is of a
yellowish colour. It feeds in oak leaves during the autumn, and
its presence is indicated by light blotches on the foliage.

Nepticula aurella


Fig. 241.—Aurella—Enlarged.

The family Nepticulidæ—the last of the Tineæ—contains a
number of little moths, including the smallest of the Lepidoptera.
Many of them are exceedingly beautiful, being decorated with[Pg 307]
various tints of a splendid metallic lustre, but their beauty is revealed
only by the use of a magnifying lens, and they are so small
that very great care and patience is required to set them properly.

They may be recognised by their short and thick antennæ,
rather large head, broad fore wings, and narrow pointed hind
wings.

The larvæ have no true legs, but have nine pairs of very
imperfectly developed claspers. They are leaf miners, and are
sometimes so abundant that several may be found in a single
leaf.

The species we have selected has fore wings of a rich golden
brown, with deep violet tips, and a broad bar of pale golden yellow
beyond the middle. It may be found throughout the spring and
summer. The larva excavates long irregular burrows in the leaves
of the bramble.[Pg 309][Pg 308]


APPENDICES

APPENDIX I

I have previously called the reader’s attention to our classified list
of butterflies and moths, and have hinted at one or two of the
objects for which it is inserted. It contains the scientific and
popular names of all the British Butterflies, Sphinges, Bombyces,
Noctuæ, and Geometræ, arranged in their various families and
genera; and in cases where two specific names are commonly
applied to the same insect, both are given.

Its chief uses to the young entomologist are to show the relation
which the insects bear one to another, and to supply a guide for
the proper arrangement of the specimens in his cabinet.

The order adopted is that of South’s ‘Synonymic List of British
Lepidoptera,’ and it has already been mentioned that similar
lists, printed on one side of the paper only, may be obtained from
dealers in naturalists’ appliances. These, cut up as required, supply
very neat labels for cabinets or store boxes.

COMPLETE CLASSIFIED LIST OF BRITISH
MACRO-LEPIDOPTERA

RHOPALOCERA (BUTTERFLIES).

  • PAPILIONIDÆ.
  • Papilio.
  • Machaon—Swallow Tail
  • PIERIDÆ.
  • Aporia.
  • Cratægi—Black-veined White
  • Pieris.
  • Brassicæ—Large White
  • Rapæ—Small White
  • Napi—Green-veined White
  • Daplidice—Bath White
  • Euchloë.
  • Cardamines—Orange Tip
  • Leucophasia.
  • Sinapis—Wood White
  • Colias.
  • Hyale—Pale Clouded Yellow
  • Edusa—Clouded Yellow
  • Gonopteryx.
  • Rhamni—Brimstone
  • NYMPHALIDÆ.
  • Argynnis.
  • Selene—Small Pearl-bordered Fritillary
    [Pg 310]
  • Euphrosyne—Pearl-bordered Fritillary
  • Latona—Queen of Spain
  • Aglaia—Dark Green Fritillary
  • Adippe—High Brown Fritillary
  • Paphia—Silver-washed Fritillary
  • Melitæa.
  • Aurinia (Artemis)—Greasy Fritillary
  • Cinxia—Glanville Fritillary
  • Athalia—Heath Fritillary
  • Vanessa.
  • C-Album—Comma
  • Polychloros—Large Tortoiseshell
  • Urticæ—Small Tortoiseshell
  • Io—Peacock
  • Antiopa—Camberwell Beauty
  • Atalanta—Red Admiral
  • Cardui—Painted Lady
  • Limenitis.
  • Sibylla—White Admiral
  • APATURIDÆ.
  • Apatura.
  • Iris—Purple Emperor
  • SATYRIDÆ.
  • Melanargia.
  • Galatea—Marbled White
  • Erebia.
  • Epiphron (Cassiope)—Small Ringlet
  • Æthiops (Blandina)—Northern Brown (Scotch Argus)
  • Pararge.
  • Egeria—Speckled Wood
  • Megæra—Wall
  • Satyrus.
  • Semele—Grayling
  • Epinephele.
  • Ianira—Meadow Brown
  • Tithonus—Large Heath (Small Meadow Brown)
  • Hyperanthes—Ringlet
  • Cænonympha.
  • Typhon (Davus)—Marsh Ringlet
  • Pamphilus—Small Heath
  • LYCÆNIDÆ.
  • Thecla.
  • Betulæ—Brown Hairstreak
  • W-Album—White-letter Hairstreak
  • Pruni—Dark Hairstreak
  • Quercus—Purple Hairstreak
  • Rubi—Green Hairstreak
  • Polyommatus.
  • Dispar—Large Copper
  • Phlœas—Small Copper
  • Lycæna.
  • Bætica—Tailed Blue
  • Ægon—Silver-studded Blue
  • Astrarche (Agestis)—Brown Argus
  • Icarus (Alexis)—Common Blue
  • Bellargus (Adonis)—Clifden Blue
  • Corydon—Chalk-hill Blue
  • Argiolus—Azure or Holly Blue
  • Semiargus (Acis)—Mazarine Blue
  • Minima (Alsus)—Small Blue
  • Arion—Large Blue
  • ERYCINIDÆ.
  • Nemeobius.
  • Lucina—Duke of Burgundy
  • HESPERIIDÆ.
  • Syrichthus.
  • Malvæ (Alveolus)—Grizzled Skipper
  • Nisoniades.
  • Tages—Dingy Skipper
  • Hesperia.
  • Thaumas (Linea)—Small Skipper
  • Lineola—New Small Skipper
  • Actæon—Lulworth Skipper
    [Pg 311]
  • Sylvanus—Large Skipper
  • Comma—Silver-spotted Skipper
  • Carterocephalus.
  • Palæmon (Paniscus)—Chequered Skipper

HETEROCERA (MOTHS).

SPHINGES.

  • SPHINGIDÆ.
  • Acherontia.
  • Atropos—Death’s Head Hawk Moth
  • Sphinx.
  • Convolvuli—Convolvulus Hawk
  • Ligustri—Privet Hawk
  • Pinastri—Pine Hawk
  • Deilephila.
  • Euphorbiæ—Spurge Hawk
  • Galii—Bedstraw Hawk
  • Livornica—Striped Hawk
  • Chærocampa.
  • Celerio—Silver-striped Hawk
  • Porcellus—Small Elephant
  • Elpenor—Large Elephant
  • Smerinthus.
  • Ocellatus—Eyed Hawk
  • Populi—Poplar Hawk
  • Tiliæ—Lime Hawk
  • Macroglossa.
  • Stellatarum—Humming-bird Hawk
  • Fuciformis—Broad-bordered Bee Hawk
  • Bombyliformis—Narrow-bordered Bee Hawk
  • SESIIDÆ.
  • Trochilium.
  • Apiformis—Hornet Clearwing of the Poplar
  • Crabroniformis (Bembeciformis)—Hornet Clearwing of Osier
  • Sciopteron.
  • Tabaniformis (Vespiforme)—Dusky Clearwing
  • Sesia.
  • Scoliiformis—Welsh Clearwing
  • Sphegiformis—White-barred Clearwing
  • Andreniformis—Orange-tailed Clearwing
  • Tipuliformis—Currant Clearwing
  • Asiliformis (Cynipiformis)—Yellow-legged Clearwing
  • Myopiformis—Red-belted Clearwing
  • Culiciformis—Large Red-belted Clearwing
  • Formiciformis—Red-tipped Clearwing
  • Ichneumoniformis—Six-belted Clearwing
  • Musciformis (Philanthiformis)—Thrift Clearwing
  • Chrysidiformis—Fiery Clearwing
  • ZYGÆNIDÆ.
  • Ino.
  • Globulariæ—Scarce Forester
  • Statices—Forester
  • Geryon—Cistus Forester
  • Zygæna.
  • Pilosellæ (Minos)—Transparent Burnet
  • Exulans—Scotch Burnet
  • Meliloti—New Forest Burnet
  • Trifolii—Broad-bordered Five-spotted Burnet
  • Loniceræ—Narrow-bordered Five-spotted Burnet
  • Filipendulæ—Six-spotted Burnet
    [Pg 312]

BOMBYCES.

  • NYCTEOLIDÆ.
  • Sarothripus.
  • Undulanus—Tortrix Moth
  • Earias.
  • Chlorana—Cream-bordered Green
  • Hylophila.
  • Prasinana—Green Silver-lined
  • Bicolorana (Quercana)—Large Green Silver-lined
  • NOLIDÆ.
  • Nola.
  • Cucullatella—Short-cloaked
  • Strigula—Small Black Arches
  • Confusalis (Cristulalis)—Least Black Arches
  • Albulalis—Kent Arches
  • Centonalis—Scarce Black Arches
  • LITHOSIIDÆ.
  • Nudaria.
  • Senex—Round-winged Muslin
  • Mundana—Muslin Moth
  • Setina.
  • Irrorella—Dew Moth
  • Calligenia.
  • Miniata—Rosy Footman (Red Arches)
  • Lithosia.
  • Mesomella—Four-dotted Footman
  • Muscerda—Dotted Footman
  • Sororcula (Aureola)—Orange Footman
  • Lutarella (Pygmæola)—Pigmy Footman
  • Griseola (Stramineola)—Pale Footman
  • Deplana (Helveola)—Buff Footman
  • Lurideola (Complanula)—Common Footman
  • Complana—Scarce Footman
  • Sericea (Molybdeola)—Leaden Footman
  • Caniola—Hoary Footman
  • Gnophria.
  • Quadra—Four-spotted Footman
  • Rubricollis—Red-necked Footman
  • Emydia.
  • Cribrum—Speckled Footman
  • EUCHELIIDÆ.
  • Deiopeia.
  • Pulchella—Crimson Speckled
  • Euchelia.
  • Jacobææ—Cinnabar
  • Callimorpha.
  • Dominula—Scarlet Tiger
  • Hera—Jersey Tiger
  • CHELONIIDÆ.
  • Nemeophila.
  • Russula—Clouded Buff
  • Plantaginis—Wood Tiger
  • Arctia.
  • Caia—Tiger
  • Villica—Cream-spot Tiger
  • Spilosoma.
  • Fuliginosa—Ruby Tiger
  • Mendica—Muslin
  • Lubricipeda—Buff Ermine
  • Menthastri—White Ermine
  • Urticæ—Water Ermine
  • HEPIALIDÆ.
  • Hepialus.
  • Humuli—Ghost Swift
  • Sylvanus—Wood Swift
  • Velleda—Northern Swift
  • Lupulinus—Common Swift
  • Hectus—Gold Swift
  • COSSIDÆ.
  • Cossus.
  • Ligniperda—Goat
  • Zeuzera.
  • Pyrina (Æsculi)—Leopard
  • Macrogaster.
    [Pg 313]
  • Castaneæ (Arundinis)—Reed Moth
  • COCHLIOPODIDÆ.
  • Heterogenea.
  • Limacodes (Testudo)—Festoon Moth
  • Asella (Asellus)—Triangle Moth
  • LIPARIDÆ.
  • Porthesia (Liparis).
  • Chrysorrhœa—Brown Tail
  • Similis (Auriflua)—Yellow Tail (Gold Tail)
  • Leucoma.
  • Salicis—Satin Moth
  • Lælia.
  • Cœnosa—Reed Tussock
  • Ocneria.
  • Dispar—Gipsy
  • Psilura.
  • Monacha—Black Arches
  • Dasychira.
  • Fascelina—Dark Tussock
  • Pudibunda—Pale Tussock
  • Orgyia.
  • Gonostigma—Scarce Vapourer
  • Antiqua—Vapourer
  • BOMBYCIDÆ.
  • Trichiura.
  • Cratægi—Pale Oak Eggar
  • Pœcilocampa.
  • Populi—December Moth
  • Eriogaster.
  • Lanestris—Small Eggar
  • Bombyx.
  • Neustria—Lackey
  • Castrensis—Ground Lackey
  • Rubi—Fox
  • Quercus—Oak Eggar
  • Trifolii—Grass Eggar
  • Odonestis.
  • Potatoria—Drinker
  • Lasiocampa.
  • Quercifolia—Lappet
  • Ilicifolia—Small Lappet
  • ENDROMIDÆ.
  • Endromis.
  • Versicolor—Kentish Glory
  • SATURNIIDÆ.
  • Saturnia.
  • Pavonia (Carpini)—Emperor
  • DREPANULIDÆ.
  • Drepana.
  • Lacertinaria (Lacertula)—Scalloped Hook Tip
  • Harpagula (Sicula)—Scarce Hook Tip
  • Falcataria (Falcula)—Pebble Hook Tip
  • Binaria (Hamula)—Oak Hook Tip
  • Cultraria (Unguicula)—Barred Hook Tip
  • Cilix.
  • Glaucata (Spinula)—Chinese Character
  • DICRANURIDÆ.
  • Dicranura.
  • Bicuspis—Alder Kitten
  • Furcula—Sallow Kitten
  • Bifida—Poplar Kitten
  • Vinula—Puss
  • Stauropus.
  • Fagi—Lobster
  • NOTODONTIDÆ.
  • Glyphisia.
  • Crenata—Dusky Marbled Brown
  • Ptilophora.
  • Plumigera—Plumed Prominent
  • Pterostoma.
  • Palpina—Pale Prominent
  • Lophopteryx.
  • Camelina—Coxcomb Prominent
  • Cuculla (Cucullina)—Maple Prominent
  • Carmelita—Scarce Prominent
  • Notodonta.
  • Bicolor—White Prominent
  • Dictæa—Swallow Prominent
    [Pg 314]
  • Dictæoides—Lesser Swallow Prominent
  • Dromedarius—Iron Prominent
  • Trilophus—Three-humped Prominent
  • Ziczac—Pebble Prominent
  • Trepida—Great Prominent
  • Trimacula (Dodonea)—Marbled Brown
  • Chaonia—Lunar Marbled Brown
  • PYGÆRIDÆ.
  • Phalera.
  • Bucephala—Buff Tip
  • Pygæra (Clostera).
  • Curtula—Chocolate Tip
  • Anachoreta—Scarce Chocolate Tip
  • Pigra (Reclusa)—Small Chocolate Tip
  • CYMATOPHORIDÆ.
  • Thyatira.
  • Derasa—Buff Arches
  • Batis—Peach Blossom
  • Cymatophora.
  • Octogesima (Ocularis)—Figure of Eighty
  • Or—Poplar Lutestring
  • Duplaris—Lesser Satin
  • Fluctuosa—Satin Carpet
  • Asphalia.
  • Diluta—Lesser Lutestring
  • Flavicornis—Yellow-horned
  • Ridens—Frosted Green

NOCTUÆ.

  • BRYOPHILIDÆ.
  • Bryophila.
  • Algæ—Tree Lichen Beauty
  • Muralis (Glandifera)—Marbled (Mottled) Green
  • Par—Scarce Marbled Green
  • Perla—Marbled Beauty
  • BOMBYCOIDÆ.
  • Moma (Diphthera).
  • Orion—Scarce Marvel-du-jour
  • Demas.
  • Coryli—Nut-tree Tussock
  • Acronycta.
  • Tridens—Dark Dagger
  • Psi—Grey Dagger
  • Leporina—Miller
  • Aceris—Sycamore
  • Megacephala—Poplar Grey
  • Strigosa—Grisette
  • Alni—Alder
  • Ligustri—Coronet
  • Rumicis—Knot-grass
  • Auricoma—Scarce Dagger
  • Menyanthidis—Light Knot-grass
  • Euphorbiæ (Myricæ)—Sweet Gale
  • Diloba.
  • Cæruleocephala—Figure of Eight
  • Arsilonche.
  • Albovenosa (Venosa)—Powdered Wainscot
  • LEUCANIIDÆ.
  • Synia.
  • Musculosa—Brighton Wainscot
  • Leucania.
  • Conigera—Brown-line Bright-eye
  • Vitellina—Delicate
  • Turca—Double Line
  • Lithargyria—Clay
  • Albipuncta—White-point
  • Extranea—American Wainscot
  • Obsoleta—Obscure Wainscot
  • Putrescens—Devonshire Wainscot
    [Pg 315]
  • Littoralis—Shore Wainscot
  • Impudens (Pudorina)—Striped Wainscot
  • Comma—Shoulder-striped Wainscot
  • Straminea—Southern Wainscot
  • Impura—Smoky Wainscot
  • Pallens—Common Wainscot
  • Calamia.
  • Phragmitidis—Fen Wainscot
  • Meliana.
  • Flammea—Flame Wainscot
  • Senta.
  • Maritima—Silky Wainscot
  • Cœnobia.
  • Rufa—Small Rufous
  • Tapinostola.
  • Fulva—Small Wainscot
  • Hellmanni—Mere Wainscot
  • Extrema (Concolor)—Concolorous Wainscot
  • Bondii—Bond’s Wainscot
  • Elymi—Lyme Wainscot
  • Nonagria.
  • Cannæ—Reed Wainscot
  • Sparganii—Iris Wainscot
  • Arundinis (Typhæ)—Bullrush
  • Geminipuncta—Twin-spotted Wainscot
  • Neurica—Nerved Wainscot
  • Brevilinea—Fenn’s Nonagria
  • Lutosa—Large Wainscot
  • APAMEIDÆ.
  • Gortyna.
  • Ochracea (Flavago)—Frosted Orange
  • Hydrœcia.
  • Nictitans—Golden Ear
  • Petasitis—Butter-bur
  • Micacea—Rosy Rustic
  • Axylia.
  • Putris—Flame
  • Xylophasia.
  • Rurea—Clouded-border Brindle
  • Lithoxylea—Light Arches
  • Sublustris—Reddish Light Arches
  • Monoglypha (Polyodon)—Dark Arches
  • Hepatica—Clouded Brindle
  • Scolopacina—Slender Clouded Brindle
  • Dipterygia.
  • Scabriuscula (Pinastri)—Bird’s Wing
  • Cloantha.
  • Polyodon (Perspicillaris)—Purple Cloud
  • Aporophyla.
  • Australis—Feathered Brindle
  • Laphygma.
  • Exigua—Small Mottled Willow
  • Neuria.
  • Reticulata (Saponariæ)—Bordered Gothic
  • Neuronia.
  • Popularis—Feathered Gothic
  • Heliophobus.
  • Hispidus—Beautiful Gothic
  • Charæas.
  • Graminis—Antler
  • Pachetra.
  • Leucophæa—Feathered Ear
  • Cerigo.
  • Matura (Cytherea)—Straw Underwing
  • Luperina.
  • Testacea—Flounced Rustic
  • Dumerili—Dumeril’s Luperina
  • Cespitis—Hedge Rustic
  • Mamestra.
  • Abjecta—Crescent Striped
  • Sordida (Anceps)—Large Nutmeg
  • Albicolon—White Colon
  • Furva—Confused
  • Brassicæ—Cabbage
    [Pg 316]
  • Persicariæ—Dot
  • Apamea.
  • Basilinea—Rustic Shoulder Knot
  • Connexa—Union Rustic
  • Gemina—Dusky Brocade
  • Unanimis—Small Clouded Brindle
  • Ophiogramma—Double Lobed
  • Leucostigma (Fibrosa)—Crescent
  • Didyma (Oculea)—Common Rustic
  • Miana.
  • Strigilis—Marbled Minor
  • Fasciuncula—Middle-barred Minor
  • Literosa—Rosy Minor
  • Bicoloria (Furuncula)—Cloaked Minor
  • Arcuosa—Dotted Buff
  • Phothedes.
  • Captiuncula—Least Minor
  • Celæna.
  • Haworthii—Haworth’s Minor
  • CARADRINIDÆ
  • Grammesia.
  • Trigrammica (Trilinea)—Treble Lines
  • Stilbia.
  • Anomala—Anomalous
  • Caradrina.
  • Morpheus—Mottled Rustic
  • Alsines—Uncertain
  • Taraxaci (Blanda)—Rustic
  • Ambigua—Ambiguous
  • Quadripunctata (Cubicularis)—Pale Mottled Willow
  • Acosmetia.
  • Caliginosa—Reddish Buff
  • Hydrilla.
  • Palustris—Marsh Moth
  • Rusina.
  • Tenebrosa—Brown Rustic
  • NOCTUIDÆ.
  • Agrotis.
  • Vestigialis (Valligera)—Archer’s Dart
  • Puta—Shuttle-shaped Dart
  • Suffusa—Dark Sword Grass
  • Saucia—Pearly Underwing
  • Segetum—Common Dart (Turnip Moth)
  • Lunigera—Crescent Dart
  • Exclamationis—Heart and Dart
  • Corticea—Heart and Club
  • Cinerea—Light Feathered Rustic
  • Ripæ—Sand Dart
  • Cursoria—Coast Dart
  • Nigricans—Garden Dart
  • Tritici—White-line Dart
  • Aquilina—Streaked Dart
  • Obelisca—Square-spot Dart
  • Agathina—Heath Rustic
  • Strigula (Porphyrea)—True Lover’s Knot
  • Præcox—Portland
  • Obscura (Ravida)—Stout Dart
  • Simulans (Pyrophila)—Dotted Rustic
  • Lucernea—Northern Rustic
  • Ashworthii—Ashworth’s Rustic
  • Noctua.
  • Glareosa—Autumn Rustic
  • Depuncta—Plain Clay
  • Augur—Double Dot
  • Plecta—Flame Shoulder
  • Flammatra—Black Collar
  • C-Nigrum—Setaceous Hebrew Character
  • Ditrapezium—Triple-spotted Clay
  • Triangulum—Double-spotted Square-spot
  • Stigmatica (Rhomboidea)—Square-spotted Clay
    [Pg 317]
  • Brunnea—Purple Clay
  • Festiva (Conflua)—Ingrailed Clay
  • Dahlii—Barred Chestnut
  • Subrosea—Rosy Marsh
  • Rubi—Small Square-spot
  • Umbrosa—Six-striped Rustic
  • Baia—Dotted Clay
  • Sobrina—Cousin German
  • Castanea (Neglecta)—Grey Rustic
  • Xanthographa—Square-spot Rustic
  • Triphæna.
  • Ianthina—Lesser Broad Border
  • Fimbria—Broad-bordered Yellow Underwing
  • Interjecta—Least Yellow Underwing
  • Orbona (Subsequa)—Lunar Yellow Underwing
  • Comes (Orbona)—Lesser Yellow Underwing
  • Pronuba—Large Yellow Underwing
  • AMPHIPYRIDÆ.
  • Amphipyra.
  • Pyramidea—Copper Underwing
  • Tragopogonis—Mouse
  • Mania.
  • Typica—Gothic
  • Maura—Old Lady
  • ORTHOSIIDÆ.
  • Panolis.
  • Piniperda—Pine Beauty
  • Pachnobia.
  • Leucographa—White-marked
  • Rubricosa—Red Chestnut
  • Hyperborea (Carnica)—Mountain Rustic
  • Tæniocampa.
  • Gothica—Hebrew Character
  • Incerta (Instabilis)—Clouded Drab
  • Opima—Northern Drab
  • Populeti—Lead-coloured Drab
  • Stabilis—Common Quaker
  • Gracilis—Powdered Quaker
  • Miniosa—Blossom Underwing
  • Munda—Twin-spotted Quaker
  • Pulverulenta (Cruda)—Small Quaker
  • Orthosia.
  • Suspecta—Suspected
  • Upsilon—Dismal
  • Lota—Red-lined Quaker
  • Macilenta—Yellow-lined Quaker
  • Anchocelis.
  • Rufina—Flounced Chestnut
  • Pistacina—Beaded Chestnut
  • Lunosa—Lunar Underwing
  • Litura—Brown-spot Pinion
  • Cerastis (Glæa).
  • Vaccinii—Chestnut
  • Spadicea—Dark Chestnut
  • Erythrocephala—Red-headed
  • Scopelosoma.
  • Satellitia—Satellite
  • Dasycampa.
  • Rubiginea—Dotted Chestnut
  • Oporina.
  • Croceago—Orange Upperwing
  • Xanthia.
  • Citrago—Orange Sallow
  • Fulvago (Cerago)—Sallow
  • Flavago (Silago)—Pink-barred Sallow
  • Aurago—Barred Sallow
  • Gilvago—Dusky Lemon Sallow
  • Circellaris (Ferruginea)—Brick
  • Cirrhœdia.
    [Pg 318]
  • Xerampelina—Centre-barred Sallow
  • COSMIIDÆ.
  • Tethea.
  • Subtusa—Olive
  • Retusa—Double Kidney
  • Cosmia (Euperia).
  • Paleacea (Fulvago)—Angle-striped Sallow
  • Dicycla.
  • Oo—Heart Moth
  • Calymnia.
  • Trapezina—Dun-bar
  • Pyralina—Lunar-spotted Pinion
  • Diffinis—White-spotted Pinion
  • Affinis—Lesser-spotted Pinion
  • HADENIDÆ.
  • Eremobia.
  • Ochroleuca—Dusky Sallow
  • Dianthœcia.
  • Luteago (Barretti)—Barrett’s Marbled Coronet
  • Cæsia—Grey Marbled Coronet
  • Nana (Conspersa)—Marbled Coronet
  • Albimacula—White Spot
  • Compta—The Shears
  • Capsincola—Lychnis
  • Cucubali—Campion
  • Carpophaga—Tawny Shears
  • Capsophila—Pod-lover
  • Irregularis (Echii)—Viper’s Bugloss
  • Hecatera.
  • Chrysozona (Dysodea)—Small Ranunculus
  • Serena—Broad-barred White
  • Polia.
  • Chi—Grey Chi
  • Flavicincta—Large Ranunculus
  • Xanthomista (Nigrocincta)—Black-banded
  • Dasypolia.
  • Templi—Brindled Ochre
  • Epunda.
  • Lichenea—Feathered Ranunculus
  • Lutulenta—Deep-brown Dart
  • Nigra—Black Rustic
  • Cleoceris.
  • Viminalis—Minor Shoulder-knot
  • Valeria.
  • Oleagina—Green-brindled Dot
  • Miselia.
  • Oxyacanthæ—Green-brindled Crescent
  • Bimaculosa—Crescent
  • Agriopis.
  • Aprilina—Marvel-du-jour
  • Euplexia.
  • Lucipara—Small Angle-shades
  • Phlogophora.
  • Meticulosa—Angle-shades
  • Trigonophora.
  • Flammea (Empyrea)—Flame Brocade
  • Aplecta.
  • Prasina (Herbida)—Green Arches
  • Occulta—Great Brocade
  • Nebulosa—Grey Arches
  • Tincta—Silvery Arches
  • Advena—Pale Shining Brown
  • Crymodes.
  • Exulis (Assimilis)—Northern Arches
  • Hadena.
  • Porphyrea (Satura)—Beautiful Brocade
  • Adusta—Dark Brocade
  • Protea—Brindled Green
  • Glauca—Glaucous Shears
  • Dentina—Grey Shears
  • Trifolii (Chenopodii)—Nutmeg
  • Atriplicis—Orache
  • Dissimilis (Suasa)—Dog’s Tooth
  • Oleracea—Bright-line Brown-eye
    [Pg 319]
  • Pisi—Broom
  • Thalassina—Pale-shouldered Brocade
  • Contigua—Beautiful Brocade
  • Genistæ—Light Brocade
  • Rectilinea—Saxon
  • XYLINIDÆ.
  • Xylocampa.
  • Areola (Lithoriza)—Early Grey
  • Xylomiges.
  • Conspicillaris—Silver Cloud
  • Calocampa.
  • Vetusta—Red Sword Grass
  • Exoleta—Sword Grass
  • Solidaginis—Golden-rod Brindled
  • Xylina.
  • Ornithopus (Rhizolitha)—Grey Shoulder Knot
  • Semibrunnea—Tawny Pinion
  • Socia (Petrificata)—Pale Pinion
  • Furcifera (Conformis)—Conformist
  • Lambda—Nonconformist
  • Asteroscopus.
  • Nubeculosa—Rannoch Sprawler
  • Sphinx (Cassinea)—Sprawler
  • Cucullia.
  • Verbasci—Mullein Shark
  • Scrophulariæ—Betony Shark
  • Lychnitis—Lychnis Shark
  • Asteris—Starwort Shark
  • Gnaphalii—Cudweed Shark
  • Absinthii—Wormwood Shark
  • Chamomillæ—Chamomile Shark
  • Umbratica—Shark
  • GONOPTERIDÆ.
  • Gonoptera.
  • Libatrix—Herald
  • PLUSIIDÆ.
  • Habrostola.
  • Tripartita (Urticæ)—Light Spectacle
  • Triplasia—Dark Spectacle
  • Plusia.
  • Chryson (Orichalcea)—Scarce Burnished Brass
  • Chrysitis—Burnished Brass
  • Bractea—Gold Spangled
  • Festucæ—Gold Spot
  • Iota—Plain Golden Y
  • Pulchrina—Beautiful Golden Y
  • Gamma—Silver Y
  • Interrogationis—Scarce Silver Y
  • HELIOTHIDÆ.
  • Anarta.
  • Melanopa—Broad-bordered White Underwing
  • Cordigera—Small Dark Yellow Underwing
  • Myrtilli—Beautiful Yellow Underwing
  • Heliaca (Heliodes).
  • Tenebrata (Arbuti)—Small Yellow Underwing
  • Heliothis.
  • Dipsacea—Marbled Clover
  • Scutosa—Rare Marbled Clover
  • Peltigera—Bordered Straw
  • Armigera—Scarce Bordered Straw
  • Chariclea.
  • Umbra (Marginata)—Bordered Sallow
  • ACONTIIDÆ.
  • Agrophila.
  • Trabealis (Sulphuralis)—Spotted Sulphur
  • Acontia.
  • Luctuosa—Four-spotted
  • ERASTRIIDÆ.
  • Erastria.
  • Fasciana (Fuscula)—Marbled White Spot
  • Venustula—Rosy Marbled
  • Bankia.
    [Pg 320]
  • Argentula—Silver-barred
  • Hydrelia.
  • Uncula (Unca)—Silver Hook
  • ANTHOPHILIDÆ.
  • Thalpochares (Micra).
  • Ostrina—Purple Marbled
  • Parva—Small Marbled
  • Paula—Scarce Marbled
  • POAPHILIDÆ.
  • Phytometra.
  • Viridaria (Ænea)—Small Purple-barred
  • EUCLIDIIDÆ.
  • Euclidia.
  • Mi—Mother Shipton
  • Glyphica—Burnet Noctua
  • OPHIUSIDÆ.
  • Ophiodes.
  • Lunaris—Lunar Double Stripe
  • CATEPHIIDÆ.
  • Catephia.
  • Alchymista—Alchymist
  • CATOCALIDÆ.
  • Catocala.
  • Fraxini—Clifden Nonpareil
  • Nupta—Red Underwing
  • Promissa—Light Crimson Underwing
  • Sponsa—Dark Crimson Underwing
  • AVENTIIDÆ.
  • Aventia.
  • Flexula—Scallop Barred
  • TOXOCAMPIDÆ.
  • Toxocampa.
  • Pastinum—Black Neck
  • Craccæ—New Black Neck
  • BOLETOBIIDÆ.
  • Boletobia.
  • Fuliginaria—Waved Black
  • HERMINIIDÆ.
  • Rivula.
  • Sericealis—Straw Dot
  • Zanclognatha.
  • Grisealis—Lesser Fan-foot
  • Tarsipennalis—Fan-foot
  • Emortualis—Olive Crescent
  • Herminia.
  • Cribralis—Dotted Fan-foot
  • Derivalis—Clay Fan-foot
  • Pechypogon.
  • Barbalis—Common Fan-foot
  • HYPENIDÆ.
  • Madopa.
  • Salicalis—Lesser Belle
  • Bomolocha.
  • Fontis (Crassalis)—Beautiful Snout
  • Hypena.
  • Rostralis—Lesser Snout
  • Proboscidalis—Snout
  • Hypenodes.
  • Albistrigalis—White-streak
  • Costæstrigalis—Ribbed-streak
  • Tholomiges (Schrankia).
  • Turfosalis—Tiny Snout
  • BREPHIDES.
  • Brephos.
  • Parthenias—Orange Underwing
  • Notha—Light Orange Underwing

GEOMETRÆ.

  • UROPTERYGIDÆ.
  • Uropteryx.
  • Sambucaria (Sambucata)—Swallow Tail
  • ENNOMIDÆ.
  • Epione.
  • Parallelaria (Vespertaria)—Dark-bordered Beauty
  • Apiciaria—Bordered Beauty
  • Advenaria—Little Thorn
  • Rumia.
  • Luteolata (Cratægata)—Brimstone
  • Venilia.
    [Pg 321]
  • Macularia—Speckled Yellow
  • Angerona.
  • Prunaria—Orange Moth
  • Metrocampa.
  • Margaritaria—Light Emerald
  • Ellopia.
  • Prosapiaria (Fasciaria)—Barred Red
  • Eurymene.
  • Dolobraria—Scorched Wing
  • Pericallia.
  • Syringaria—Lilac Beauty
  • Selenia.
  • Bilunaria (Illunaria)—Early Thorn
  • Lunaria—Lunar Thorn
  • Tetralunaria (Illustraria)—Purple Thorn
  • Odontopera.
  • Bidentata—Scalloped Hazel
  • Crocallis.
  • Elinguaria—Scalloped Oak
  • Eugonia.
  • Autumnaria (Alniaria)—Large Thorn
  • Alniaria (Tiliaria)—Canary-shouldered Thorn
  • Fuscantaria—Dusky Thorn
  • Erosaria—September Thorn
  • Quercinaria (Angularia)—August Thorn
  • Himera.
  • Pennaria—Feathered Thorn
  • AMPHIDASYDÆ.
  • Phigalia.
  • Pedaria (Pilosaria)—Pale Brindled Beauty
  • Nyssia.
  • Zonaria—Belted Beauty
  • Hispidaria—Small Brindled Beauty
  • Lapponaria—Rare Brindled Beauty
  • Biston.
  • Hirtaria—Brindled Beauty
  • Amphidasys.
  • Strataria (Prodromaria)—Oak Beauty
  • Betularia—Peppered Moth
  • BOARMIIDÆ.
  • Hemerophila.
  • Abruptaria—Waved Umber
  • Cleora.
  • Angularia (Viduaria)—Speckled Beauty
  • Glabraria—Dotted Carpet
  • Lichenaria—Brussels Lace
  • Boarmia.
  • Repandata—Mottled Beauty
  • Gemmaria (Rhomboidaria)—Willow Beauty
  • Abietaria—Satin Carpet
  • Cinctaria—Ringed Carpet
  • Roboraria—Great Oak Beauty
  • Consortaria—Pale Oak Beauty
  • Tephrosia.
  • Consonaria—Square Spot
  • Crepuscularia—Small Engrailed
  • Biundularia—Engrailed
  • Luridata (Extersaria)—Brindled White-spot
  • Punctularia—Grey Birch
  • Gnophos.
  • Obscuraria—Annulet
  • Dasydia.
  • Obfuscaria—Scotch Annulet
  • Psodos.
  • Coracina (Trepidaria)—Black Mountain Moth
  • GEOMETRIDÆ.
  • Pseudoterpna.
  • Pruinata (Cytisaria)—Grass Emerald
  • Geometra.
  • Papilionaria—Large Emerald
  • Vernaria—Small Emerald
  • Phorodesma.
    [Pg 322]
  • Pustulata (Bajularia)—Blotched Emerald
  • Smaragdaria—Essex Emerald
  • Nemoria.
  • Viridata—Small Grass Emerald
  • Iodis.
  • Lactearia—Little Emerald
  • Hemithea.
  • Strigata (Thymiaria)—Common Emerald
  • EPHYRIDÆ.
  • Zonosoma.
  • Porata—False Mocha
  • Punctaria—Maiden’s Blush
  • Linearia (Trilinearia)—Clay Triple-lines
  • Annulata (Omicronaria)—Mocha
  • Orbicularia—Dingy Mocha
  • Pendularia—Birch Mocha
  • ACIDALIIDÆ.
  • Hyria.
  • Muricata (Auroraria)—Golden-bordered Purple
  • Asthena.
  • Luteata—Small Yellow Wave
  • Candidata—Small White Wave
  • Sylvata—Waved Carpet
  • Blomeri (Pulchraria)—Blomer’s Rivulet
  • Eupisteria.
  • Obliterata (Heparata)—Dingy Shell
  • Venusia.
  • Cambrica (Cambricaria)—Welsh Wave
  • Acidalia.
  • Perochraria—Ochraceous Wave
  • Ochrata—Bright Wave
  • Rubiginata (Rubricata)—Tawny Wave
  • Dimidiata (Scutulata)—Single-dotted Wave
  • Bisetata—Small Fan-footed Wave
  • Trigeminata—Treble Brown-spot
  • Contiguaria—Greening’s Wave
  • Rusticata—Least Carpet
  • Holosericata—Silky Wave
  • Dilutaria (Interjectaria)—Dark Cream Wave
  • Virgularia (Incanaria)—Small Dusty Wave
  • Circellata—Circellate
  • Ornata—Lace Border
  • Marginepunctata (Promutata)—Mullein Wave
  • Straminata—Dotted-bordered Cream Wave
  • Subsericeata—Satin Wave
  • Immutata—Lesser Cream Wave
  • Strigaria—Streaked Wave
  • Remutaria—Cream Wave
  • Fumata—Smoky Wave
  • Strigilaria (Prataria)—Sub-angled Wave
  • Imitaria—Small Blood-vein
  • Emutaria—Rosy Wave
  • Aversata—Riband Wave
  • Inornata—Plain Wave
  • Degeneraria—Portland Riband Wave
  • Emarginata—Small Scallop
  • Timandra.
  • Amataria—Blood-vein
  • CABERIDÆ.
  • Cabera.
  • Pusaria—Common White Wave
  • Rotundaria—Round-winged Wave
  • Exanthemata—Common Wave
  • Bapta.
  • Temerata—Clouded Silver
    [Pg 323]
  • Bimaculata (Taminata)—White-pinion Spotted
  • Aleucis.
  • Pictaria—Sloe Carpet
  • MACARIIDÆ.
  • Macaria.
  • Alternata—Sharp-angled Peacock
  • Notata—Peacock
  • Liturata—Tawny-barred Angle
  • Halia.
  • Vauaria (Wavaria)—V Moth
  • Brunneata (Pinetaria)—Rannoch Geometer
  • FIDONIIDÆ.
  • Strenia.
  • Clathrata—Latticed Heath
  • Panagra.
  • Petraria—Brown Silver-line
  • Numeria.
  • Pulveraria—Barred Umber
  • Scodiona.
  • Belgiaria—Grey Scalloped Bar
  • Selidosema.
  • Ericetaria (Plumaria)—Bordered Grey
  • Fidonia.
  • Carbonaria—Netted Mountain
  • Limbaria (Conspicuata)—Frosted Yellow
  • Ematurga.
  • Atomaria—Common Heath
  • Bupalus.
  • Piniaria—Bordered White
  • Minoa.
  • Murinata (Euphorbiata)—Drab Geometer
  • Scoria.
  • Lineata (Dealbata)—Black-veined
  • Aplasta.
  • Ononaria—Rest-harrow
  • Sterrha.
  • Sacraria—Vestal
  • Lythria.
  • Purpuraria—Purple-barred Yellow
  • Aspilates.
  • Strigillaria—Grass Wave
  • Ochrearia (Citraria)—Yellow Belle
  • Gilvaria—Straw Belle
  • ZERENIDÆ.
  • Abraxas.
  • Grossulariata—Currant Moth (Magpie)
  • Sylvata (Ulmata)—Clouded Magpie
  • Ligdia.
  • Adustata—Scorched Carpet
  • Lomaspilis.
  • Marginata—Clouded Border
  • LIGIIDÆ.
  • Pachycnemia.
  • Hippocastanaria—Horse Chestnut
  • HYBERNIIDÆ.
  • Hybernia.
  • Rupicapraria—Early Moth
  • Leucophæaria—Spring Usher
  • Aurantiaria—Scarce Umber
  • Marginaria (Progemmaria)—Dotted Border
  • Defoliaria—Mottled Umber
  • Anisopteryx.
  • Æscularia—March Moth
  • LARENTIIDÆ.
  • Cheimatobia.
  • Brumata—Winter Moth
  • Boreata—Northern WinterMoth
  • Oporabia.
  • Dilutata—November Moth
  • Filigrammaria—Autumnal Moth
  • Autumnaria
  • Larentia.
  • Didymata—Twin-spot Carpet
  • Multistrigaria—Mottled Grey
    [Pg 324]
  • Cæsiata—Grey Mountain Carpet
  • Flavicinctata (Ruficinctata)—Yellow-ringed Carpet
  • Salicata—Striped Twin-spot Carpet
  • Olivata—Beech-green Carpet
  • Viridaria (Pectinitaria)—Green Carpet
  • Emmelesia.
  • Affinitata—Rivulet
  • Alchemillata—Small Rivulet
  • Albulata—Grass Rivulet
  • Decolorata—Sandy Carpet
  • Tæniata—Barred Carpet
  • Unifasciata—Haworth’s Carpet
  • Minorata (Ericetata)—Heath Rivulet
  • Adæquata (Blandiata)—Pretty Pinion
  • Eupithecia.
  • Venosata—Netted Pug
  • Consignata—Pinion-spotted Pug
  • Linariata—Toadflax Pug
  • Pulchellata—Foxglove Pug
  • Oblongata (Centaureata)—Lime-speck
  • Succenturiata—Bordered Lime-speck
  • Subfulvata—Tawny-speckled Pug
  • Scabiosata (Subumbrata)—Shaded Pug
  • Pernotata—Guenée’s Pug
  • Plumbeolata—Lead-coloured Pug
  • Isogrammaria—Haworth’s Pug
  • Pygmæata—Marsh Pug
  • Helveticaria—Edinburgh Pug
  • Egenaria—Pauper Pug
  • Satyrata—Satyr Pug
  • Castigata—Grey Pug
  • Jasioneata—Jasione Pug
  • Trisignaria—Triple-spotted Pug
  • Virgaureata—Golden-rod Pug
  • Fraxinata—Ash-tree Pug
  • Extensaria—Scarce Pug
  • Pimpinellata—Pimpinel Pug
  • Valerianata—Valerian Pug
  • Pusillata—Dwarf Pug
  • Irriguata—Marbled Pug
  • Campanulata—Campanula Pug
  • Innotata—Long-winged Pug
  • Indigata—Ochreous Pug
  • Constrictata—Wild Thyme Pug
  • Nanata—Narrow-winged Pug
  • Subnotata—Plain Pug
  • Vulgata—Common Pug
  • Albipunctata—White-spotted Pug
  • Expallidata—Bleached Pug
  • Absinthiata—Wormwood Pug
  • Minutata—Ling Pug
  • Assimilata—Currant Pug
  • Tenuiata—Slender Pug
  • Subciliata—Maple Pug
  • Lariciata—Larch Pug
  • Abbreviata—Brindled Pug
  • Dodoneata—Oak-tree Pug
  • Exiguata—Mottled Pug
  • Ultimaria—Tamarisk Pug
  • Sobrinata—Juniper Pug
  • Togata—Cloaked Pug
  • Pumilata—Double-striped Pug
  • CoronataV Pug
  • Rectangulata—Green Pug
  • Debiliata—Bilberry Pug
  • Collix.
  • Sparsata—Dentated Pug
  • Lobophora.
  • Sexalisata (Sexalata)—Small Seraphim
  • Halterata (Hexapterata)—Seraphim
    [Pg 325]
  • Viretata—Yellow-barred Brindle
  • Carpinata (Lobulata)—Early Tooth-striped
  • Polycommata—Barred Tooth-striped
  • Thera.
  • Juniperata—Juniper Carpet
  • Simulata—Chestnut-coloured Carpet
  • Variata (Obeliscata)—Shaded Broad-bar
  • Firmata—Pine Carpet
  • Hypsipetes.
  • Ruberata—Ruddy High-flier
  • Trifasciata (Impluviata)—May High-flier
  • Sordidata (Elutata)—July High-flier
  • Melanthia.
  • Bicolorata (Rubiginata)—Blue-bordered Carpet
  • Ocellata—Purple Bar
  • Albicillata—Beautiful Carpet
  • Melanippe.
  • Hastata—Argent and Sable
  • Tristata—Small Argent and Sable
  • Procellata—Chalk Carpet
  • Unangulata—Sharp-angled Carpet
  • Rivata—Wood Carpet
  • Sociata (Subtristata)—Common Carpet
  • Montanata—Silver-ground Carpet
  • Galiata—Galium Carpet
  • Fluctuata—Garden Carpet
  • Anticlea.
  • Cucullata (Sinuata)—Royal Mantle
  • Rubidata—Flame
  • Badiata—Shoulder Stripe
  • Nigrofasciaria (Derivata)—Streamer
  • Berberata—Barberry Carpet
  • Coremia.
  • Munitata—Red Carpet
  • Designata (Propugnata)—Flame Carpet
  • Ferrugata—Red Twin-spot Carpet
  • Unidentaria—Dark-barred Twin-spot Carpet
  • Quadrifasciaria—Large Twin-spot Carpet
  • Camptogramma.
  • Bilineata—Yellow Shell
  • Fluviata—Gem
  • Phibalapteryx.
  • Tersata—Fern
  • Lapidata—Slender-striped Rufous
  • Vittata (Lignata)—Oblique Carpet
  • Polygrammata (Conjunctaria)—Many-lined
  • Vitalbata—Small Waved Umber
  • Triphosa.
  • Dubitata—Tissue
  • Eucosmia.
  • Certata—Scarce Tissue
  • Undulata—Scalloped Shell
  • Scotosia.
  • Vetulata—Brown Scallop
  • Rhamnata—Dark Umber
  • Cidaria.
  • Siterata (Psittacata)—Red-green Carpet
  • Miata—Autumn Green Carpet
  • Picata—Short-cloak Carpet
  • Corylata—Broken-barred Carpet
  • Sagittata—Marsh Carpet
  • Truncata (Russata)—Common Marbled Carpet
  • Immanata—Dark Marbled Carpet
  • Suffumata—Water Carpet
  • Reticulata—Netted Carpet
  • Silaceata—Small Phœnix
  • Prunata (Ribesiaria)—Phœnix
    [Pg 326]
  • Testata—Chevron
  • Populata—Northern Spinach
  • Fulvata—Barred Yellow
  • Dotata (Pyraliata)—Barred Straw
  • Associata (Dotata)—Spinach
  • Pelurga.
  • Comitata—Dark Spinach
  • EUBOLIIDÆ.
  • Eubolia.
  • Cervinata (Cervinaria)—Mallow
  • Limitata (Mensuraria)—Small Mallow
  • Plumbaria (Palumbaria)—Belle
  • Bipunctaria—Chalk Carpet
  • Mesotype.
  • Virgata (Lineolata)—Oblique-striped
  • Carsia.
  • Paludata (Imbutata)—Manchester Treble Bar
  • Anaitis.
  • Plagiata—Treble Bar
  • Lithostege.
  • Griseata—Pale Grey Carpet
  • Chesias.
  • Spartiata—Streak
  • Rufata (Obliquaria)—Broom Tip
  • SIONIDÆ.
  • Tanagra.
  • Atrata (Chærophyllata)—Chimney Sweep

APPENDIX II

THE LEPIDOPTERIST’S CALENDAR

The success of the country rambles of an expert lepidopterist depends
greatly on his knowledge of the times at which the various
butterflies and moths generally appear, and of the localities which
they are known to frequent. The experiences he has gained in the
past enable him to calculate on the probabilities of the future, and
he chooses both time and locality according to his requirements.

As he makes his way to the hunting ground he counts over the
chances of meeting with a certain insect that is wanted to fill a
long-standing blank in his cabinet; and we hear him discussing the
probabilities as to whether this species is yet ‘out,’ or whether the
larvæ of that species are feeding.

How different it is with the young and unguided entomologist!
He rambles promiscuously here and there, having only the faintest
idea as to what he is likely to see, and perhaps meeting with only
four or five species when an experienced collector, without covering
a larger area of ground, would take scores in the same time.

In order to afford some little help to the beginner, I have
thought it advisable to introduce a calendar of operations to guide
him in his work. The space at our command would not allow this
to be carried out in detail, but the general instructions will undoubtedly
assist most of my readers until the practical experience
gained by a few years’ work has enabled them to run on their own legs.[Pg 327]

Of course, in making reference to the monthly lists of insects on
the wing, allowance must be made for the forwardness or backwardness
of the seasons. Thus, an insect entered in the April list may
appear in March in an exceptionally warm season, but may not
emerge till the early part of May if the spring has been unusually
severe.

It will be observed that in cases where all the species of a
certain genus or family appear on the wing in the same month, the
name of that genus or family is entered on the list instead of the
names of the individual species; but the latter can easily be obtained
by reference to Appendix I.

JANUARY

There is not much field work to be done during this month. If
the weather is very severe, hardly an insect will be found on the
wing; but a mild January will sometimes entice the Brimstone
Butterfly (Rhamni) and some of the hybernating Vanessas from
their winter quarters.

Hybernating moths may also be met with, on the wing if the
weather is mild, or sleeping in their sheltered nooks during the
frosts. These include several NoctuæAuricoma, Lithargyria,
Suffusa, Vaccinii, Spadicea, Erythrocephala, Satellitia, Rubiginea,
Croceago, Vetusta, Exoleta, Ornithopus, Furcifera, Semibrunnea,
Socia, and Libatrix; and also a few GeometræZonaria,
Fluviata, Dubitata, Siterata, and Miata.

In addition to these hybernating insects, the collector may
examine tree trunks and fences for the Early Moth (Rupicapraria),
and late specimens of the Winter Moth (Brumata); and towards the
end of the month he may expect to meet with fresh specimens of
the Pale Brindled Beauty (Pedaria) and the Spring Usher (Leucophæaria).
A few of the Tineæ may also be seen.

The net need not be used at all during the colder months of the
year, as the moths are easily taken in pill boxes from the trunks
and fences on which they rest.

Pupa digging may be carried on throughout the month if the
weather is sufficiently mild, but it is of no use attempting this
during a frost. Hybernating larvæ may also be searched out of
their winter quarters if the collector does not mind giving them the
attention they require; but, as a rule, it is better to wait till they
themselves start out to feed in the spring, at which time all their
food plants are showing leaf.

FEBRUARY

Our remarks under ‘January’ concerning pupa digging and
other work apply equally well to this month. The same hybernating
butterflies and moths may be looked for; and, in addition to[Pg 328]
Pedaria, Leucophæaria, and Rupicapraria, which now appear
more plentifully, the following species will probably be seen:

  • Small Eggar (Lanestris)
  • Small Brindled Beauty (Hispidaria)
  • Oak Beauty (Strataria)
  • Dotted Border (Marginaria)
  • March Moth (Æscularia)

About half a dozen species of the Tineæ will also have made
their appearance before the end of the month.

MARCH

Many of the hybernating larvæ will come out during March if
the weather is mild, and commence to feed; and the young caterpillars
will begin to appear from the eggs of the early moths already
named. This is consequently a good time to commence the search
for larvæ if you intend to go in for rearing. During the daytime
some may be beaten from the boughs of trees and shrubs; and those
which feed on low plants, being generally nocturnal in their habits,
should be searched for in the evening, after dark, with the aid of a
lantern.

The hybernating butterflies are now flying more freely than
before, and, if the weather is bright and warm for the time of year,
a few freshly emerged species may be seen. These may possibly
include:

  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Holly Blue (Argiolus)

As regards moths, several fresh species may be expected to
appear, while those named as appearing in February are still to be
found. The new-comers may include:

  • Bombyces.
  • Kentish Glory (Versicolor)
  • Yellow-horned (Flavicornis)
  • Noctuæ.
  • Pine Beauty (Piniperda)
  • White-marked Rustic (Leucographa)
  • Red Chestnut (Rubricosa)
  • All species of the genus Tæniocampa
  • Early Grey (Areola)
  • Green-brindled Dot (Oleagina)
  • Orange Underwing (Parthenias)
  • Light Orange Underwing (Notha)
  • Geometræ.
  • Early Thorn (Bilunaria)
  • Engrailed (Biundularia)
  • Mottled Grey (Multistrigaria)

Sugaring may be commenced towards the end of March, and
sallow blossom may be searched in the evening, but it is probable
that only a few species will be taken by these means.

A few more species of the Tineæ appear in March, and four or
five of the Tortrices are out before the end of the month.[Pg 329]

APRIL

This is really a busy month with the entomologist, and it will
be necessary to put all apparatus and appliances into perfect order
early. The cyanide bottle should be freshly charged, nets examined
and repaired if necessary, and all setting boards, breeding cages
&c. put in perfect trim for the new season’s work.

Larvæ are now feeding freely, and a few hours spent in beating,
sweeping, and searching will enable you to stock your cages
liberally.

Sugaring may be continued throughout the month, and the
sallow blossom may be searched as long as it proves attractive.
Moths may also be attracted by light at night.

The following butterflies are generally out during April, in
addition to the hybernated species already named:

  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Orange Tip (Cardamines)
  • Wood White (Sinapis)
  • Pearl-bordered Fritillary (Euphrosyne)
  • Speckled Wood (Egeria)
  • Green Hairstreak (Rubi)
  • Small Copper (Phlœas)
  • Holly Blue (Argiolus)
  • Grizzled Skipper (Malvæ)
  • Dingy Skipper (Tages)

The following is a list of the principal moths for April:

  • Bombyces.
  • Small Lappet (Ilicifolia)
  • Kentish Glory (Versicolor)
  • Yellow Horned (Flavicornis)
  • Frosted Green (Ridens)
  • Noctuæ.
  • Pine Beauty (Piniperda)
  • White-marked Rustic (Leucographa)
  • Red Chestnut (Rubricosa)
  • All species of the genus Tæniocampa
  • Early Grey (Areola)
  • Mullein Shark (Verbasci)
  • Orange Underwing (Parthenias)
  • Light Orange Underwing (Notha)
  • Geometræ.
  • Brimstone (Luteolata)
  • Early Thorn (Bilunaria)
  • Belted Beauty (Zonaria)
  • Brindled Beauty (Hirtaria)
  • Waved Umber (Abruptaria)
  • Small Engrailed (Crepuscularia)
  • Engrailed (Biundularia)
  • Sloe Carpet (Pictaria)
  • Netted Mountain (Carbonaria)
  • Mottled Grey (Multistrigaria)
  • Satyr Pug (Satyrata)
  • Marbled Pug (Irriguata)
  • Campanula Pug (Campanulata)
  • Brindled Pug (Abbreviata)
  • Oak-tree Pug (Dodoneata)
  • Double-striped Pug (Pumilata)
  • Early Tooth-striped (Carpinata)
  • Shoulder Stripe (Badiata)
  • Many-lined (Polygrammata)
  • Tissue (Dubitata)

[Pg 330]

In addition to the above, a few species of the Tortrices, several
of the Tineæ, and one or two of the Plume Moths (Pterophori) are
out during April.

MAY

Little or nothing will be obtained by digging during May, yet a
number of pupæ may be found among grass and leaves under
trees, and also attached to the leaves and stems of low plants.
These pupæ include those of several of the butterflies, among which
may be mentioned Machaon, Selene, Euphrosyne, Aurinia, Megæra,
Ianira, Rubi, Astrarche, Icarus, Bellargus, Corydon, Lucina, and
Sylvanus.

Larvæ may now be taken in abundance by beating the boughs
of oaks and other trees, and also by examining low plants.

The hybernating butterflies are still on the wing, and the
following are also out:

  • Swallow Tail (Machaon)
  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Bath White (Daplidice)
  • Orange Tip (Cardamines)
  • Wood White (Sinapis)
  • Small Pearl-bordered (Selene)
  • Pearl-bordered (Euphrosyne)
  • Greasy Fritillary (Aurinia)
  • Glanville Fritillary (Cinxia)
  • Speckled Wood (Egeria)
  • Wall (Megæra)
  • Marsh Ringlet (Typhon)
  • Small Heath (Pamphilus)
  • Green Hairstreak (Rubi)
  • Small Copper (Phlœas)
  • Brown Argus (Astrarche)
  • Common Blue (Icarus)
  • Clifden Blue (Bellargus)
  • Holly Blue (Argiolus)
  • Mazarine Blue (Semiargus)
  • Grizzled Skipper (Malvæ)
  • Chequered Skipper (Palæmon)

There is a great increase in the number of moths this month,
and much good work may be done by means of light traps and by
the examination of fences. Many moths are driven from their
resting places early in the morning by the direct rays of the rising
sun, and then seek out a spot where they are better sheltered, and
where they are consequently less easily found. Hence the advantage
of searching fences early in the morning.

The May list includes:

  • Sphinges.
  • Small Elephant (Porcellus)
  • All species of the genera Smerinthus and Macroglossa
  • Some of the Clearwings (Apiformis, Sphegiformis, and Culiciformis)
  • Cream-bordered Green (Chlorana)
  • Green Silver-lined (Prasinana)
  • Bombyces.
  • Wood Tiger (Plantaginis)
  • Muslin Moth (Mendica)
  • Common Swift (Lupulinus)
  • Pale Tussock (Pudibunda)
  • Small Lappet (Ilicifolia)
  • Emperor (Pavonia)
  • All species of family Drepanulidæ
    [Pg 331]
  • Alder Kitten (Bicuspis)
  • Puss (Vinula)
  • Several of the ‘Prominents’ (Cuculla, Carmelita, Dictæa, Dictæoides, Trilophus, Ziczac, Trepida, Chaonia, Trimacula)
  • Chocolate Tip (Curtula)
  • Small Chocolate Tip (Pigra)
  • Noctuæ.
  • Knot Grass (Rumicis)
  • Sweet Gale (Myricæ)
  • White Colon (Albicolon)
  • Cabbage (Brassicæ)
  • Treble Lines (Trigrammica)
  • Marsh Moth (Palustris)
  • Light Brocade (Genistæ)
  • Mullein Shark (Verbasci)
  • Betony Shark (Scrophulariæ)
  • Starwort Shark (Asteris)
  • Camomile Shark (Chamomillæ)
  • Small Dark Yellow Underwing (Cordigera)
  • Small Yellow Underwing (Tenebrata)
  • Bordered Sallow (Umbra)
  • Lunar Double Stripe (Lunaris)
  • Geometræ.
  • Brimstone (Luteolata)
  • Speckled Yellow (Macularia)
  • Purple Thorn (Tetralunaria)
  • Scalloped Hazel (Bidentata)
  • Brindled Beauty (Hirtaria)
  • Peppered (Betularia)
  • Waved Umber (Abruptaria)
  • Ringed Carpet (Cinctaria)
  • Square Spot (Consonaria)
  • Small Engrailed (Crepuscularia)
  • Engrailed (Biundularia)
  • Grey Birch (Punctularia)
  • Small Grass Emerald (Viridata)
  • All species of family Ephyridæ
  • Cream Wave (Remutaria)
  • White Wave (Pusaria)
  • Round-winged Wave (Rotundaria)
  • Common Wave (Exanthemata)
  • Clouded Silver (Temerata)
  • White-pinion Spotted (Bimaculata)
  • Latticed Heath (Clathrata)
  • Brown Silver-line (Petraria)
  • Barred Umber (Pulveraria)
  • Netted Mountain (Carbonaria)
  • Common Heath (Atomaria)
  • Bordered White (Piniaria)
  • Rest Harrow (Ononaria)
  • Yellow Belle (Ochrearia)
  • Clouded Border (Marginata)
  • Horse Chestnut (Hippocastanaria)
  • Pretty Pinion (Adæquata)
  • Pugs (Venosata, Consignata, Pulchellata, Plumbeolata, Satyrata, Castigata, Pusillata, Irriguata, Indigata, Nanata, Vulgata, Assimilata, Exiguata, Coronata)
  • Yellow-barred Brindle (Viretata)
  • Ruddy High-flier (Ruberata)
  • May High-flier (Trifasciata)
  • Common Carpet (Sociata)
  • Silver-ground Carpet (Montanata)
  • Streamer (Nigrofasciaria)
  • Barberry Carpet (Berberata)
  • Flame Carpet (Designata)
  • Twin-spot Carpets (Ferrugata and Unidentaria)
  • Scarce Tissue (Certata)
  • Water Carpet (Suffumata)
  • Small Phœnix (Silaceata)
  • Oblique-striped (Virgata)
  • Broom Tip (Rufata)

A number of the Micros are also out this month. About twenty
species of the Pyralides, one or two of the Pterophori, a few
Crambi, about fifty of the Tortrices, and no less than two hundred
of the Tineæ. The collector will do well to search fences and[Pg 332]
tree trunks for these moths, whenever he has the opportunity; and
also to use the net freely in wooded country, waste places, and
along hedgerows, before and at dusk.

JUNE

There is a marked increase in winged insect life during this
month. The early butterflies are disappearing, or perhaps have
quite left us; but new species are taking their place. The
Sphinges now reach their maximum, as do also the Bombyces; and
the other groups are almost if not quite up to their highest total.
The Noctuæ and Geometræ each amount to over a hundred species.
No less than a hundred and fifty British Tortrices are on the wing;
the Tineæ make a near approach to three hundred, and the Pyralides
of the month are not far short of numbering a hundred species.
It will thus be seen that the net and pill boxes, as well as the setting
boards, are in constant demand.

Dull days may be well occupied in beating for moths, and in the
examination of fences and the bark of trees; and on bright days,
as soon as the butterflies have settled down to rest, the same work
may be carried on till dusk.

Micros and Geometræ are out early in the evening, when they
should be taken with the net. Later on the Noctuæ may be seen
playing round their favourite flowers.

Sugar and light traps are likely to do good service during June,
and decoy females of the Bombyces group may be called to your
aid.

Larvæ are also abundant during June, and those of most of the
butterflies may be taken by carefully searching their food plants.

The following is the list of imagines for the month:

  • Butterflies.
  • Swallow Tail (Machaon)
  • Black-veined White (Cratægi)
  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Small Pearl-bordered (Selene)
  • Pearl-bordered (Euphrosyne)
  • Silver-washed Fritillary (Paphia)
  • Greasy Fritillary (Aurinia)
  • Glanville Fritillary (Cinxia)
  • Heath Fritillary (Athalia)
  • Small Tortoiseshell (Urticæ)
  • White Admiral (Sibylla)
  • Small Ringlet (Epiphron)
  • Meadow Brown (Ianira)
  • Ringlet (Hyperanthus)
  • Marsh Ringlet (Typhon)
  • Small Heath (Pamphilus)
  • Green Hairstreak (Rubi)
  • Small Copper (Phlœas)
  • Common Blue (Icarus)
  • Small Blue (Minima)
  • Duke of Burgundy (Lucina)
  • Grizzled Skipper (Malvæ)
  • Dingy Skipper (Tages)
  • Large Skipper (Sylvanus)
  • Chequered Skipper (Palæmon)
  • Sphinges.
  • Privet Hawk (Ligustri)
  • Spurge Hawk (Euphorbiæ)
  • Small Elephant (Porcellus)
  • Large Elephant (Elpenor)
    [Pg 333]
  • Eyed Hawk (Ocellatus)
  • Poplar Hawk (Populi)
  • Lime Hawk (Tiliæ)
  • Humming Bird Hawk (Stellatarum)
  • All the Clearwings (Sesiidæ)
  • The Burnets (Fam. Zygænidæ)
  • Bombyces.
  • Family Nolidæ
  • Dew Moth (Irrorella)
  • Cinnabar (Jacobææ)
  • Scarlet Tiger (Dominula)
  • Family Cheloniidæ
  • Family Hepialidæ
  • Family Cossidæ
  • Family Cochliopodidæ
  • Dark Tussock (Fascelina)
  • Pale Tussock (Pudibunda)
  • Scarce Vapourer (Gonostigma)
  • Fox (Rubi)
  • Lappet (Quercifolia)
  • Family Drepanulidæ
  • Family Dicranuridæ
  • Pale Prominent (Palpina)
  • Coxcomb Prominent (Camelina)
  • Swallow Prominent (Dictæa)
  • Lesser Swallow Prominent (Dictæoides)
  • Iron Prominent (Dromedarius)
  • Pebble Prominent (Ziczac)
  • Great Prominent (Trepida)
  • Marbled Brown (Trimacula)
  • Buff Tip (Bucephala)
  • Peach Blossom (Batis)
  • Genus Cymatophora
  • Noctuæ.
  • Scarce Marvel-du-jour (Orion)
  • Genus Acronycta
  • Powdered Wainscot (Albovenosa)
  • Most of the species of genus Leucania
  • Flame Wainscot (Flammea)
  • Silky Wainscot (Maritima)
  • Small Rufous (Rufa)
  • Mere Wainscot (Hellmanni)
  • Concolorous (Extrema)
  • Flame (Putris)
  • Genus Xylophasia
  • Bird’s Wing (Scabriuscula)
  • Small Mottled Willow (Exigua)
  • Bordered Gothic (Reticulata)
  • Feathered Ear (Leucophæa)
  • Large Nutmeg (Sordida)
  • White Colon (Albicolon)
  • Cabbage (Brassicæ)
  • Dot (Persicariæ)
  • Rustic Shoulder Knot (Basilinea)
  • Union Rustic (Connexa)
  • Dusky Brocade (Gemina)
  • Double Lobed (Ophiogramma)
  • Genus Miana
  • Treble Lines (Trigrammica)
  • Mottled Rustic (Morpheus)
  • Rustic (Taraxaci)
  • Pale Mottled Willow (Quadripunctata)
  • Reddish Buff (Caliginosa)
  • Marsh Moth (Palustris)
  • Brown Rustic (Tenebrosa)
  • Turnip (Segetum)
  • Heart and Dart (Exclamationis)
  • Light-feathered Rustic (Cinerea)
  • Sand Dart (Ripæ)
  • Garden Dart (Nigricans)
  • Lover’s Knot (Strigula)
  • Double Dot (Augur)
  • Flame Shoulder (Plecta)
  • Double-spotted Square-spot (Triangulum)
  • Ingrailed Clay (Festiva)
  • Broad-bordered Yellow Underwing (Fimbria)
  • Large Yellow Underwing (Pronuba)
  • Gothic (Typica)
  • Heart Moth (Oo)
  • Genus Dianthœcia
  • Broad-barred White (Serena)
    [Pg 334]
  • Small Angle Shades (Lucipara)
  • Angle Shades (Meticulosa)
  • Green Arches (Prasina)
  • Grey Arches (Nebulosa)
  • Silvery Arches (Tincta)
  • Pale Shining Brown (Advena)
  • Northern Arches (Exulis)
  • Genus Hadena (nearly all)
  • Lychnis Shark (Lychnitis)
  • Starwort Shark (Asteris)
  • Cudweed Shark (Gnaphalii)
  • Camomile Shark (Chamomillæ)
  • Shark (Umbratica)
  • Genus Habrostola
  • Burnished Brass (Chrysitis)
  • Plain Golden Y (Iota)
  • Beautiful Golden Y (Pulchrina)
  • Silver Y (Gamma)
  • Scarce Silver Y (Interrogationis)
  • Genus Anarta
  • Small Yellow Underwing (Tenebrata)
  • Bordered Straw (Peltigera)
  • Bordered Sallow (Umbra)
  • Spotted Sulphur (Trabealis)
  • Four-spotted (Luctuosa)
  • Family Erastriidæ
  • Purple Marbled (Ostrina)
  • Small Marbled (Parva)
  • Small Purple-barred (Viridaria)
  • Mother Shipton (Mi)
  • Burnet Noctua (Glyphica)
  • Black Neck (Pastinum)
  • Family Herminiidæ
  • Family Hypenidæ
  • Geometræ.
  • Little Thorn (Advenaria)
  • Brimstone (Luteolata)
  • Speckled Yellow (Macularia)
  • Orange (Prunaria)
  • Barred Red (Prosapiaria)
  • Scorched Wing (Dolobraria)
  • Lunar Thorn (Lunaria)
  • Peppered (Betularia)
  • Speckled Beauty (Angularia)
  • Genus Boarmia
  • Square Spot (Consonaria)
  • Brindled White-spot (Luridata)
  • Grey Birch (Punctularia)
  • Blotched Emerald (Pustulata)
  • Small Grass Emerald (Viridata)
  • Common Emerald (Strigata)
  • Nearly all the family Acidaliidæ
  • Genus Bapta
  • Peacock (Notata)
  • Rannoch Geometer (Brunneata)
  • Brown Silver-line (Petraria)
  • Barred Umber (Pulveraria)
  • Grey Scalloped Bar (Belgiaria)
  • Frosted Yellow (Limbaria)
  • Bordered White (Piniaria)
  • Drab Geometer (Murinata)
  • Black-veined (Lineata)
  • Grass Wave (Strigillaria)
  • Clouded Magpie (Sylvata)
  • Scorched Carpet (Adustata)
  • Clouded Border (Marginata)
  • Twin-spot Carpet (Didymata)
  • Grey Mountain Carpet (Cæsiata)
  • Striped Twin-spot Carpet (Salicata)
  • Green Carpet (Viridaria)
  • Genus Emmelesia
  • Most of the Pugs (Eupithecia)
  • Small Seraphim (Sexalisata)
  • Seraphim (Halterata)
  • Yellow-barred Brindle (Viretata)
  • Shaded Broad-bar (Variata)
  • Ruddy High-flier (Ruberata)
  • Purple Bar (Ocellata)
  • Beautiful Carpet (Albicillata)
  • Genus Melanippe
  • Royal Mantle (Cucullata)
  • Flame (Rubidata)
  • Genus Coremia
    [Pg 335]
  • Yellow Shell (Bilineata)
  • Fern (Tersata)
  • Oblique Carpet (Vittata)
  • Small Waved Umber (Vitalbata)
  • Scalloped Shell (Undulata)
  • Brown Scallop (Vetulata)
  • Short-cloak Carpet (Picata)
  • Broken-barred Carpet (Corylata)
  • Common Marbled Carpet (Truncata)
  • Small Phœnix (Silaceata)
  • Small Mallow (Limitata)
  • Belle (Plumbaria)
  • Oblique-striped (Virgata)
  • Treble Bar (Plagiata)
  • Pale Grey Carpet (Griseata)
  • Chimney Sweep (Atrata)

JULY

The number of species on the wing in July is even greater than
in June. Butterflies are very numerous, some being second broods
of double-brooded species, and others late single-brooded insects.

Sphinges are beginning to fall off, and so are the Bombyces,
but the Noctuæ and Geometræ are slightly on the increase.

As regards the Micros, a good number of fresh species may be
expected, all the groups exhibiting a marked increase in the total
number on the wing with the exception of the Tineæ.

Sugaring is likely to pay well this month, and many moths
may be attracted by light. Tree trunks and fences should be well
examined.

Pupæ may certainly be taken, but unless the collector is particularly
desirous of obtaining the pupæ of insects known to be now
passing through that stage, he will probably do better by looking
after imagines.

Larvæ, however, may well receive a little attention, providing
the setting of butterflies and moths leave a little leisure for other
employments. Beating by day, and searching by both day and
night, even if carried on only occasionally, will probably supply
you with as many species as you can accommodate in your glasses
and cages.

The butterflies of the month are:

  • Swallow Tail (Machaon)
  • Black-veined White (Cratægi)
  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Wood White (Sinapis)
  • Brimstone (Rhamni)
  • Dark Green Fritillary (Aglaia)
  • High Brown Fritillary (Adippe)
  • Silver-washed Fritillary (Paphia)
  • Heath Fritillary (Athalia)
  • Comma (C-Album)
  • Large Tortoiseshell (Polychloros)
  • Small Tortoiseshell (Urticæ)
  • Peacock (Io)
  • Painted Lady (Cardui)
  • White Admiral (Sibylla)
  • Purple Emperor (Iris)
  • Marbled White (Galatea)
  • Northern Brown (Æthiops)
  • Speckled Wood (Egeria)
  • Grayling (Semele)
  • Meadow Brown (Ianira)
    [Pg 336]
  • Large Heath (Tithonus)
  • Ringlet (Hyperanthes)
  • Marsh Ringlet (Typhon)
  • Small Heath (Pamphilus)
  • Brown Hairstreak (Betulæ)
  • White-letter Hairstreak (W-Album)
  • Dark Hairstreak (Pruni)
  • Purple Hairstreak (Quercus)
  • Green Hairstreak (Rubi)
  • Small Copper (Phlœas)
  • Silver-studded Blue (Ægon)
  • Common Blue (Icarus)
  • Chalk-hill Blue (Corydon)
  • Holly Blue (Argiolus)
  • Mazarine Blue (Semiargus)
  • Small Blue (Minima)
  • Large Blue (Arion)
  • Small Skipper (Thaumas)
  • New Small Skipper (Lineola)

The moths of July include the following species:

  • Sphinges.
  • Privet Hawk (Ligustri)
  • Bedstraw Hawk (Galii)
  • Eyed Hawk (Ocellatus)
  • Poplar Hawk (Populi)
  • Humming Bird Hawk (Stellatarum)
  • Hornet Clearwing of Poplar (Apiformis)
  • Hornet Clearwing of Osier (Crabroniformis)
  • Welsh Clearwing (Scoliiformis)
  • Red-belted Clearwing (Myopiformis)
  • Red-tipped Clearwing (Formiciformis)
  • Six-belted Clearwing (Ichneumoniformis)
  • Genus Ino
  • Burnets (Trifolii, Loniceræ and Filipendulæ)
  • Bombyces.
  • Tortrix (Undulanus)
  • Large Green Silver-lined (Bicolorana)
  • Short-cloaked (Cucullatella)
  • Most of the family Lithosiidæ
  • Tiger (Caia)
  • Ruby Tiger (Fuliginosa)
  • Buff Ermine (Lubricipeda)
  • White Ermine (Menthastri)
  • Wood Swift (Sylvanus)
  • Northern Swift (Velleda)
  • Goat Moth (Ligniperda)
  • Leopard (Pyrina)
  • Brown Tail (Chrysorrhœa)
  • Yellow Tail (Similis)
  • Satin (Salicis)
  • Reed Tussock (Cœnosa)
  • Black Arches (Monacha)
  • Vapourer (Antiqua)
  • Lackey (Neustria)
  • Ground Lackey (Castrensis)
  • Oak Eggar (Quercus)
  • Drinker (Potatoria)
  • Sallow Kitten (Furcula)
  • Poplar Kitten (Bifida)
  • Lobster (Fagi)
  • Pale Prominent (Palpina)
  • Coxcomb Prominent (Camelina)
  • Buff Tip (Bucephala)
  • Buff Arches (Derasa)
  • Peach Blossom (Batis)
  • Figure of Eighty (Octogesima)
  • Poplar Lutestring (Or)
  • Lesser Satin (Duplaris)
  • Noctuæ.
  • Marbled Green (Muralis)
  • Marbled Beauty (Perla)
  • Grey Dagger (Psi)
  • Miller (Leporina)
  • Poplar Grey (Megacephala)
  • Grisette (Strigosa)
  • Coronet (Ligustri)
  • Knot Grass (Rumicis)
  • Scarce Dagger (Auricoma)
  • Light Knot Grass (Menyanthidis)
    [Pg 337]
  • Brown Line Bright Eye (Conigera)
  • Double Line (Turca)
  • Clay (Lithargyria)
  • Wainscots (Littoralis, Impudens, Comma, Impura, Pallens, Phragmitidis, Maritima, Rufa, Bondii, Neurica)
  • Ear Moth (Nictitans)
  • Flame (Putris)
  • Genus Xylophasia
  • Antler (Graminis)
  • Straw Underwing (Matura)
  • Most of Genus Mamestra
  • Genus Miana
  • Haworth’s Minor (Haworthii)
  • Treble Lines (Trigrammica)
  • Genus Caradrina
  • Brown Rustic (Tenebrosa)
  • Archer’s Dart (Vestigialis)
  • Pearly Underwing (Saucia)
  • Heart and Dart (Exclamationis)
  • Heart and Club (Corticea)
  • Sand Dart (Ripæ)
  • Coast Dart (Cursoria)
  • Garden Dart (Nigricans)
  • Streaked Dart (Aquilina)
  • True Lover’s Knot (Strigula)
  • Stout Dart (Obscura)
  • Dotted Rustic (Simulans)
  • Northern Rustic (Lucernea)
  • Ashworth’s Rustic (Ashworthii)
  • Most of Genus Noctua
  • Genus Triphæna
  • Copper Underwing (Pyramidea)
  • Mouse (Tragopogonis)
  • Old Lady (Maura)
  • Suspected (Suspecta)
  • Dismal (Upsilon)
  • Olive (Subtusa)
  • Genus Calymnia
  • Dusky Sallow (Ochroleuca)
  • Marbled Coronet (Nana)
  • Genus Hecatera
  • Minor Shoulder Knot (Viminalis)
  • Small Angle Shades (Lucipara)
  • Genus Aplecta
  • Dark Brocade (Adusta)
  • Shears (Dentina)
  • Nutmeg (Trifolii)
  • Pale-shouldered Brocade (Thalassina)
  • Silver Cloud (Conspicillaris)
  • Lychnis Shark (Lychnitis)
  • Wormwood Shark (Absinthii)
  • Family Plusiidæ
  • Beautiful Yellow Underwing (Myrtilli)
  • Marbled Clover (Dipsacea)
  • Four-spotted (Luctuosa)
  • Rosy Marbled (Venustula)
  • Marbled White-spot (Fasciana)
  • Small Purple-barred (Viridaria)
  • Red Underwing (Nupta)
  • Light Crimson Underwing (Promissa)
  • Dark Crimson Underwing(Sponsa)
  • New Black-neck (Craccæ)
  • Family Herminiidæ
  • Family Hypenidæ
  • Geometræ.
  • Swallow-tail (Sambucaria)
  • Dark-bordered Beauty (Parallelaria)
  • Bordered Beauty (Apiciaria)
  • Orange (Prunaria)
  • Light Emerald (Margaritaria)
  • Barred Red (Prosapiaria)
  • Lilac Beauty (Syringaria)
  • Early Thorn (Bilunaria)
  • Scalloped Oak (Elinguaria)
  • Genus Cleora
  • Genus Boarmia
  • Annulet (Obscuraria)
  • Scotch Annulet (Obfuscaria)
  • Black Mountain Moth (Coracina)
  • Family Geometridæ
  • Golden-bordered Purple (Muricata)
    [Pg 338]
  • Waved Carpet (Sylvata)
  • Dingy Shell (Obliterata)
  • Welsh Wave (Cambrica)
  • Most of the Acidaliæ
  • Blood Vein (Amataria)
  • Family Macariidæ
  • Latticed Heath (Clathrata)
  • Bordered Grey (Ericetaria)
  • Common Heath (Atomaria)
  • Rest Harrow (Ononaria)
  • Vestal (Sacraria)
  • Grass Wave (Strigillaria)
  • Family Zerenidæ
  • Twin-spot Carpet (Didymata)
  • Grey Mountain Carpet (Cæsiata)
  • Yellow-ringed Carpet (Flavicinctata)
  • Beech-green Carpet (Olivata)
  • Green Carpet (Viridaria)
  • Genus Emmelesia
  • Pugs (Linariata, Oblongata, Succenturiata, Pernotata, Isogrammaria, Virgaureata, Innotata, Subnotata, Absinthiata, Tenuiata, Subciliata, Rectangulata)
  • Chestnut-coloured Carpet (Simulata)
  • Shaded Broad Bar (Variata)
  • Pine Carpet (Firmata)
  • July High-flier (Sordidata)
  • Genus Melanthia
  • Genus Melanippe
  • Flame (Rubidata)
  • Red Carpet (Munitata)
  • Large Twin-spot Carpet (Quadrifasciaria)
  • Yellow Shell (Bilineata)
  • Fern (Tersata)
  • Oblique Carpet (Vittata)
  • Many-lined (Polygrammata)
  • Dark Umber (Rhamnata)
  • Short-cloak Carpet (Picata)
  • Marsh Carpet (Sagittata)
  • Common Marbled Carpet (Truncata)
  • Dark Marbled Carpet (Immanata)
  • Netted Carpet (Reticulata)
  • Phœnix (Prunata)
  • Chevron (Testata)
  • Northern Spinach (Populata)
  • Barred Yellow (Fulvata)
  • Barred Straw (Dotata)
  • Spinach (Associata)
  • Dark Spinach (Comitata)
  • Small Mallow (Limitata)
  • Belle (Plumbaria)
  • Chalk Carpet (Bipunctaria)
  • Oblique-striped (Virgata)
  • Manchester Treble Bar (Paludata)
  • Treble Bar (Plagiata)
  • Pale Grey Carpet (Griseata)
  • Chimney Sweep (Atrata)

AUGUST

Although there is a very appreciable falling off in the number
of species on the wing during August, yet there remains plenty
of work for the lepidopterist.

Many of the butterflies of July continue to fly during the whole
or part of this month, and several fresh species commence their
flight. August, too, may be looked upon as the month for second
broods, and an opportunity now arises for searching for some of the
species that were missed at the time of their early appearance in
May. Clover and lucerne fields should be well worked.

A few Sphinges and a number of the Bombyces are still on the
wing. The Noctuæ are on the decrease, but there are yet nearly
a hundred species (including the rarer ones) at large.[Pg 339]

These last may be taken at sugar in considerable numbers, and
it is interesting to note that two of the Vanessas (Atalanta and
Cardui) may be caught sipping on your baited trees during the
daytime.

Geometræ and Micros fall off very considerably this month, but
these, as well as moths of the other groups, may be taken from
tree trunks and palings. Light traps may also be used with much
success during August.

Fallen fruits should be examined for the larvæ that feed within
them; and late in the month ripe fruit will supply food to the
lovers of sweets.

Ivy blossom should be well worked at night; and clover and
lucerne fields form admirable hunting grounds for moths at night,
especially just after rain.

Larvæ are to be obtained in abundance by beating and searching,
the latter process being conducted by night as well as by day.

The following is the list of imagines for August:

  • Butterflies.
  • Swallow Tail (Machaon)
  • Large White (Brassicæ)
  • Small White (Rapæ)
  • Green-veined White (Napi)
  • Bath White (Daplidice)
  • Wood White (Sinapis)
  • Pale Clouded Yellow (Hyale)
  • Clouded Yellow (Edusa)
  • Brimstone (Rhamni)
  • Queen of Spain (Latona)
  • Dark Green Fritillary (Aglaia)
  • High Brown Fritillary (Adippe)
  • Silver-washed Fritillary (Paphia)
  • Genus Vanessa
  • White Admiral (Sibylla)
  • Purple Emperor (Iris)
  • Marbled White (Galatea)
  • Northern Brown (Æthiops)
  • Speckled Wood (Egeria)
  • Wall (Megæra)
  • Grayling (Semele)
  • Meadow Brown (Ianira)
  • Large Heath (Tithonus)
  • Small Heath (Pamphilus)
  • Brown Hairstreak (Betulæ)
  • Purple Hairstreak (Quercus)
  • Small Copper (Phlœas)
  • Tailed Blue (Bætica)
  • Silver-studded Blue (Ægon)
  • Brown Argus (Astrarche)
  • Common Blue (Icarus)
  • Clifden Blue (Bellargus)
  • Chalk-hill Blue (Corydon)
  • Holly Blue (Argiolus)
  • Mazarine Blue (Semiargus)
  • Dingy Skipper (Tages)
  • New Small Skipper (Lineola)
  • Lulworth Skipper (Actæon)
  • Large Skipper (Sylvanus)
  • Silver-spotted Skipper (Comma)
  • Sphinges.
  • Death’s-head Hawk (Atropos)
  • Convolvulus Hawk (Convolvuli)
  • Bedstraw Hawk (Galii)
  • Striped Hawk (Livornica)
  • Humming Bird Hawk (Stellatarum)
  • Red-tipped Clearwing (Formiciformis)
  • Six-belted Clearwing (Ichneumoniformis)
  • Bombyces.
  • Round-winged Muslin (Senex)
  • Muslin (Mundana)
  • Footmen (Muscerda, Lutarella, Griseola)
    [Pg 340]
  • Wood Swift (Sylvanus)
  • Brown Tail (Chrysorrhœa)
  • Yellow Tail (Similis)
  • Satin (Salicis)
  • Gipsy (Dispar)
  • Black Arches (Monacha)
  • Vapourer (Antiqua)
  • Lackey (Neustria)
  • Ground Lackey (Castrensis)
  • Oak Eggar (Quercus)
  • Grass Eggar (Trifolii)
  • Drinker (Potatoria)
  • Hook Tips (Lacertinaria, Falcataria, Binaria, Cultraria)
  • Chinese Character (Glaucata)
  • Sallow Kitten (Furcula)
  • Poplar Kitten (Bifida)
  • Prominents (Camelina, Trilophus, Ziczac)
  • Lesser Lutestring (Diluta)
  • Noctuæ.
  • Marbled Green (Muralis)
  • Marbled Beauty (Perla)
  • Grey Dagger (Psi)
  • Scarce Dagger (Auricoma)
  • Wainscots (Musculosa, Albipuncta, Impura, Pallens, Fulva, Cannæ, Arundinis, Geminipuncta, Neurica, Lutosa)
  • Frosted Orange (Ochracea)
  • Genus Hydrœcia
  • Slender Clouded Brindle (Scolopacina)
  • Feathered Brindle (Australis)
  • Feathered Gothic (Popularis)
  • Antler (Graminis)
  • Straw Underwing (Matura)
  • Genus Luperina
  • Confused (Furva)
  • Small Clouded Brindle (Unanimis)
  • Crescent (Leucostigma)
  • Common Rustic (Didyma)
  • Anomalous (Anomala)
  • Mottled Rustic (Morpheus)
  • Pale Mottled Willow (Quadripunctata)
  • Archer’s Dart (Vestigialis)
  • Shuttle-shaped Dart (Puta)
  • Pearly Underwing (Saucia)
  • Crescent Dart (Lunigera)
  • Heart and Dart (Exclamationis)
  • Coast Dart (Cursoria)
  • Garden Dart (Nigricans)
  • White-line Dart (Tritici)
  • Streaked Dart (Aquilina)
  • Square-spot Dart (Obelisca)
  • Heath Rustic (Agathina)
  • Portland (Præcox)
  • Stout Dart (Obscura)
  • Dotted Rustic (Simulans)
  • Plain Clay (Depuncta)
  • Setaceous Hebrew Character (C-Nigrum)
  • Barred Chestnut (Dahlii)
  • Small Square-spot (Rubi)
  • Six-striped Rustic (Umbrosa)
  • Grey Rustic (Castanea)
  • Square-spot Rustic (Xanthographa)
  • Genus Triphæna
  • Mouse (Tragopogonis)
  • Old Lady (Maura)
  • Mountain Rustic (Hyperborea)
  • Suspected (Suspecta)
  • Olive (Subtusa)
  • Double Kidney (Retusa)
  • Angle-striped Sallow (Paleacea)
  • Genus Calymnia
  • Dusky Sallow (Ochroleuca)
  • Grey Chi (Chi)
  • Large Ranunculus (Flavicincta)
  • Feathered Ranunculus (Lichenea)
  • Crescent (Bimaculosa)
  • Great Brocade (Occulta)
  • Beautiful Brocade (Porphyrea)
  • Golden-rod Brindled (Solidaginis)
  • Herald (Libatrix)
    [Pg 341]
  • Scarce Burnished Brass (Chryson)
  • Burnished Brass (Chrysitis)
  • Gold Spot (Festucæ)
  • Scarce Bordered Straw (Armigera)
  • Four-spotted (Luctuosa)
  • Clifden Nonpareil (Fraxini)
  • Red Underwing (Nupta)
  • Dark Crimson Underwing (Sponsa)
  • Geometræ.
  • Dark-bordered Beauty (Parallelaria)
  • Bordered Beauty (Apiciaria)
  • Purple Thorn (Tetralunaria)
  • Scalloped Oak (Elinguaria)
  • Canary-shouldered Thorn (Alniaria)
  • Dusky Thorn (Fuscantaria)
  • September Thorn (Erosaria)
  • August Thorn (Quercinaria)
  • Dotted Carpet (Glabraria)
  • Annulet (Obscuraria)
  • Scotch Annulet (Obfuscaria)
  • Family Ephyridæ
  • Small Dusty Wave (Virgularia)
  • Mullein Wave (Marginepunctata)
  • Small Blood Vein (Imitaria)
  • Common White Wave (Pusaria)
  • Vestal (Sacraria)
  • Yellow Belle (Ochrearia)
  • Straw Belle (Gilvaria)
  • Currant (Grossulariata)
  • Autumnaria
  • Haworth’s Carpet (Unifasciata)
  • Bordered Lime Speck (Succenturiata)
  • Pugs (Virgaureata, Campanulata, Indigata, Constrictata, Expallidata, Sobrinata, Variata)
  • July High Flier (Sordidata)
  • Carpets (Bicolorata, Montanata, Fluctuata, Berberata)
  • Yellow Shell (Bilineata)
  • Gem (Fluviata)
  • Oblique Carpet (Vittata)
  • Many-lined (Polygrammata)
  • Tissue (Dubitata)
  • Common Marbled Carpet (Truncata)
  • Phœnix (Prunata)
  • Chevron (Testata)
  • Northern Spinach (Populata)
  • Barred Yellow (Fulvata)
  • Barred Straw (Dotata)
  • Small Mallow (Limitata)
  • Chalk Carpet (Bipunctaria)
  • Treble Bar (Plagiata)
  • Broom Tip (Rufata)

SEPTEMBER

The number of species on the wing is now considerably lower, yet
there is a good deal to be done both with butterflies and moths.

Many of the former are worn and ragged, but good fresh
specimens of some species may be taken. Clover and lucerne
fields and the flowery borders of corn fields remain very attractive.

Tree trunks and palings should be searched as before. Sugar
still attracts numbers of the Noctuæ; and ivy blossom should
be examined at night whenever an opportunity offers itself.

September is a good month for larva hunting. Most of the
species that pupate in the autumn are now full fed, and will
undergo the change to the chrysalis state shortly after they have
been housed, thus giving but little trouble to the entomologist.
The day feeders may be beaten or swept from their food plants, but,[Pg 342]
of course, the nocturnal species are best discovered by searching at
night.

Some have already ‘gone down’ for the winter, and, consequently,
pupa hunting may be started. However, as there is
yet much to be done with imagines and larvæ, it may, perhaps, be
better to leave the pupæ alone till about the end of the month,
especially as many of the larvæ have not yet had time to complete
their transformation.

The list of imagines for September includes:

  • Butterflies.
  • Clouded Yellow (Edusa)
  • Brimstone (Rhamni)
  • Queen of Spain (Latona)
  • Comma (C-Album)
  • Large Tortoiseshell (Polychloros)
  • Small Tortoiseshell (Urticæ)
  • Peacock (Io)
  • Camberwell Beauty (Antiopa)
  • Red Admiral (Atalanta)
  • Painted Lady (Cardui)
  • Speckled Wood (Egeria)
  • Wall (Megæra)
  • Grayling (Semele)
  • Large Heath (Tithonus)
  • Small Heath (Pamphilus)
  • Small Copper (Phlœas)
  • Common Blue (Icarus)
  • Clifden Blue (Bellargus)
  • Chalk-hill Blue (Corydon)
  • Holly Blue (Argiolus)
  • Sphinges.
  • Death’s-head Hawk (Atropos)
  • Convolvulus Hawk (Convolvuli)
  • Humming Bird Hawk (Stellatarum)
  • Bombyces.
  • Tortrix (Undulanus)
  • Crimson Speckled (Pulchella)
  • Vapourer (Antiqua)
  • Pale Oak Eggar (Cratægi)
  • Lesser Lutestring (Diluta)
  • Noctuæ.
  • Figure of Eight (Cæruleocephala)
  • Small Wainscot (Fulva)
  • Bullrush (Arundinis)
  • Large Wainscot (Lutosa)
  • Frosted Orange (Ochracea)
  • Rosy Rustic (Micacea)
  • Feathered Brindle (Australis)
  • Beautiful Gothic (Hispidus)
  • Antler (Graminis)
  • Flounced Rustic (Testacea)
  • Hedge Rustic (Cespitis)
  • Haworth’s Minor (Haworthii)
  • Anomalous (Anomala)
  • Shuttle-shaped Dart (Puta)
  • Dark Sword Grass (Suffusa)
  • Pearly Underwing (Saucia)
  • Turnip (Segetum)
  • Heart and Dart (Exclamationis)
  • Autumn Rustic (Glareosa)
  • Mouse (Tragopogonis)
  • Red-lined Quaker (Lota)
  • Yellow-lined Quaker (Macilenta)
  • Genus Anchocelis
  • Genus Xanthia
  • Centre-barred Sallow (Xerampelina)
  • Double Kidney (Retusa)
  • Genus Polia
  • Black Rustic (Nigra)
  • Green-brindled Crescent (Oxyacanthæ)
  • Marvel-du-jour (Aprilina)
  • Angle Shades (Meticulosa)
  • Flame Brocade (Flammea)
  • Brindled Green (Protea)
  • Genus Calocampa
  • Genus Xylina
  • Herald (Libatrix)
    [Pg 343]
  • Gold Spot (Festucæ)
  • Silver Y (Gamma)
  • Scarce Bordered Straw (Armigera)
  • Clifden Nonpareil (Fraxini)
  • Buttoned Snout (Rostralis)
  • Geometræ.
  • Bordered Beauty (Apiciaria)
  • Brimstone (Luteolata)
  • Genus Eugonia
  • November (Dilutata)
  • Autumnal (Filigrammaria)
  • Juniper Pug (Sobrinata)
  • Shaded Broad Bar (Variata)
  • Slender-striped Rufous (Lapidata)
  • Tissue (Dubitata)
  • Carpets (Siderata, Miata, Immanata)
  • Chevron (Testata)
  • Mallow (Cervinata)
  • Streak (Spartiata)

OCTOBER

As there is very little winged life this month, and the larvæ have
nearly all sought out their winter quarters, special attention may be
given to pupæ. The earlier this work is started after the insects
have completed their change the better. If left late, many pupæ
will have been destroyed by floods, moles, &c., and a prolonged
series of frosty days may render digging unproductive if not impossible.
Again, it must be remembered that some larvæ are not
yet down, and by digging at the roots of the trees on which they are
feeding, you are preparing an acceptable bed for the late species,
for the pupæ of which you may call again in about a month.

Larvæ may be obtained by beating and searching as before, but
this work should be done as early in the month as possible, since
but few are feeding after the first week or so.

Butterfly catching is now practically over, only a few of the late
species and the hybernators being on the wing, and these only on
mild days.

Noctuæ are still attracted by sugar and ivy blossom, and a few
may be found at rest. Geometræ and Micros may be taken
from palings and tree trunks by day, or caught flying at dusk.

The imagines of October may include the following butterflies:

  • Brimstone (Rhamni)
  • Pale Clouded Yellow (Hyale)
  • Clouded Yellow (Edusa)
  • Comma (C-Album)
  • Large Tortoiseshell (Polychloros)
  • Small Tortoiseshell (Urticæ)
  • Peacock (Io)
  • Camberwell Beauty (Antiopa)
  • Red Admiral (Atalanta)
  • Painted Lady (Cardui)
  • Small Copper (Phlœas)

And a few late ‘Blues.’

The principal moths of the month are:

  • Sphinges.
  • Death’s-head Hawk (Atropos)
  • Bombyces.
  • Plumed Prominent (Plumigera)
  • Noctuæ.
  • Large Wainscot (Lutosa)
  • Red-lined Quaker (Lota)
    [Pg 344]
  • Yellow-lined Quaker (Macilenta)
  • Beaded Chestnut (Pistacina)
  • Brown-spot Pinion (Litura)
  • Chestnut (Vaccinii)
  • Dark Chestnut (Spadicea)
  • Red-headed Chestnut (Erythrocephala)
  • Satellite (Satellitia)
  • Dotted Chestnut (Rubiginea)
  • Orange Upperwing (Croceago)
  • Brick (Circellaris)
  • Brindled Ochre (Templi)
  • Green Brindled Crescent (Oxyacanthæ)
  • Marvel-du-jour (Aprilina)
  • Angle Shades (Meticulosa)
  • Flame Brocade (Flammea)
  • Red Sword-grass (Vetusta)
  • Sword-grass (Exolita)
  • Genus Xylina
  • Sprawler (Sphinx)
  • Silver Y (Gamma)
  • Geometræ.
  • Feathered Thorn (Pennaria)
  • Vestal (Sacraria)
  • Scarce Umber (Aurantiaria)
  • Mottled Umber (Defoliaria)
  • Winter (Brumata)
  • Northern Winter (Boreata)
  • November (Dilutata)
  • Juniper Carpet (Juniperata)
  • Gem (Fluviata)
  • Carpets (Siderata, Miata)
  • Mallow (Cervinata)
  • Streak (Spartiata)

NOVEMBER

No butterflies are to be seen this month with the exception of
the hybernating species, and even these will not venture on the wing
unless the weather is mild and bright for the season.

Most of the moths met with are also hybernators, but a few
species are to be found only at this season, and these should be
looked for on fences and tree trunks. A few Noctuæ may be taken
at sugar, and the Geometræ attracted by lights.

The only larvæ now existing are hybernators, and many of these
may be met with during your pupa-digging operations; but they are
best left alone till the spring, as a rule.

The chief work of the entomologist in November is certainly
pupa hunting, and this may be carried on in real earnest whenever
the weather is favourable, following the instructions given in
Chapter VII.

It will be remembered, also, that many of the Lepidoptera pass
the winter in the egg state, and search may be made for ova when
time permits.

The November list, besides some of the hybernating species
previously mentioned, include:

  • Bombyces.
  • December (Populi)
  • Noctuæ.
  • Genus Cerastis
  • Satellite (Satellitia)
  • Dotted Chestnut (Rubiginea)
  • Orange Upperwing (Croceago)
  • Brindled Ochre (Exempli)
  • Geometræ.
  • Feathered Thorn (Pennaria)
  • Scarce Umber (Aurantiaria)
  • Mottled Umber (Defoliaria)
  • Winter (Brumata)
  • Northern Winter (Boreata)

[Pg 345]

DECEMBER

Outdoor work is now at a minimum. The weather is too severe,
as a rule, to allow pupa digging to be carried on with either success
or comfort, but favourable opportunities should be seized for this
employment as well as for ova collecting.

Now and again we may meet with P. Populi at rest by day, or
fluttering round a light at night. Brumata and Defoliaria may
also be seen, and the Early Moth (Rupicapraria) may appear on
the wing before the new year; but nothing is likely to be met with
beyond these save the hybernators, already named in other lists,
and some of the Tineæ.

It is a good plan to utilise your spare time during the dreary
months of winter by attending to your cabinet. Rearrange your
specimens where necessary, and see that all are properly labelled;
remove all greasy specimens, and deal with them as recommended
on page 127; also renew the supply of camphor or naphthaline in
your drawers and store boxes. Time may also be found for the
construction of apparatus that is likely to be required next season,
and for repairing any that has been damaged during the work of
the last.[Pg 346]


[Pg 347]

COLOURED PLATES

Plate I (Frontispiece)

  1. Swallow-tail (Papilio Machaon).
  2. Black-veined White (Aporia Cratægi).
  3. Large White (Pieris Brassicæ). Female.
  4. Small White (Pieris Rapæ). Male.
  5. Green-veined White (Pieris Napi). Under side.
  6. Bath White (Pieris Daplidice). Female.
  7. Orange Tip (Euchloë Cardamines). Male.
  8. Orange Tip (Euchloë Cardamines). Male. Under side.

Plate II

  1. Wood White (Leucophasia Sinapis).
  2. Pale Clouded Yellow (Colias Hyale).
  3. Clouded Yellow (Colias Edusa). Male.
  4. Brimstone (Gonopteryx Rhamni). Male.
  5. Small Pearl-bordered Fritillary (Argynnis Selene).
  6. Pearl-bordered Fritillary (Argynnis Euphrosyne).
  7. Queen of Spain Fritillary (Argynnis Latona).
  8. Dark-green Fritillary (Argynnis Aglaia).

Plate III

  1. High Brown Fritillary (Argynnis Adippe). Under side.
  2. Silver-washed Fritillary (Argynnis Paphia).
  3. Greasy Fritillary (Melitæa Aurinia).
  4. Glanville Fritillary (Melitæa Cinxia).
  5. Heath Fritillary (Melitæa Athalia).
  6. Heath Fritillary (Melitæa Athalia). Under side.
  7. Comma (Vanessa C-Album).
  8. Large Tortoiseshell (Vanessa Polychloros).
  9. Small Tortoiseshell (Vanessa Urticæ).

[Pg 348]

Plate IV

  1. Peacock (Vanessa Io).
  2. Camberwell Beauty (Vanessa Antiopa).
  3. Red Admiral (Vanessa Atalanta).
  4. Painted Lady (Vanessa Cardui).
  5. White Admiral (Limenitis Sibylla).

Plate V

  1. Purple Emperor (Apatura Iris). Male.
  2. Marbled White (Melanargia Galatea).
  3. Small Ringlet (Erebia Epiphron).
  4. Northern Brown (Erebia Æthiops).
  5. Wood Argus (Pararge Egeria).
  6. Wall Butterfly (Pararge Megæra).
  7. Grayling (Satyrus Semele). Female.
  8. Meadow Brown (Epinephele Ianira). Female.
  9. Large Heath (Epinephele Tithonus). Male.
  10. Ringlet (Epinephele Hyperanthus).

Plate VI

  1. Marsh Ringlet (Cænonympha Typhon).
  2. Small Heath (Cænonympha Pamphilus).
  3. Brown Hairstreak (Thecla Betulæ). Under side.
  4. White-letter Hairstreak (Thecla W-album). Under side.
  5. Dark Hairstreak (Thecla Pruni). Under side.
  6. Purple Hairstreak (Thecla Quercus). Under side.
  7. Green Hairstreak(Thecla Rubi). Under side.
  8. Large Copper (Polyommatus Dispar). Male.
  9. Small Copper (Polyommatus Phlæas).
  10. Tailed Blue (Lycæna Bætica).
  11. Silver-studded Blue (Lycæna Ægon). Male.
  12. Silver-studded Blue (Lycæna Ægon). Female.
  13. Brown Argus (Lycæna Astrarche).
  14. Brown Argus (Lycæna Astrarche). Under side.
  15. Common Blue (Lycæna Icarus). Male.
  16. Common Blue (Lycæna Icarus). Female.
  17. Clifden Blue (Lycæna Bellargus). Male.
  18. Clifden Blue (Lycæna Bellargus). Female.

[Pg 349]

Plate VII

  1. Chalk-hill Blue (Lycæna Corydon). Male.
  2. Chalk-hill Blue (Lycæna Corydon). Female.
  3. Holly Blue (Lycæna Argiolus). Male.
  4. Holly Blue (Lycæna Argiolus). Female.
  5. Mazarine Blue (Lycæna Semiargus). Male.
  6. Mazarine Blue (Lycæna Semiargus). Female.
  7. Small Blue (Lycæna Minima).
  8. Large Blue (Lycæna Arion).
  9. Duke of Burgundy Fritillary (Nemeobius Lucina).
  10. Duke of Burgundy Fritillary (Nemeobius Lucina). Under side.
  11. Grizzled Skipper (Syrichthus Malvæ).
  12. Dingy Skipper (Nisoniades Tages).
  13. Small Skipper (Hesperia Thaumas).
  14. Lulworth Skipper (Hesperia Actæon). Male.
  15. Large Skipper (Hesperia Sylvanus). Male.
  16. Silver-spotted Skipper (Hesperia Comma).
  17. Chequered Skipper (Carterocephalus Palæmon).
  18. New Small Skipper (Hesperia Lineola).

Plate VIII

  1. Larva of Swallow-tail Butterfly (Papilio Machaon).
  2. Larva of Orange Tip (Euchloë Cardamines).
  3. Larva of Silver-washed Fritillary (Argynnis Paphia).
  4. Larva of Peacock Butterfly (Vanessa Io).
  5. Larva of Purple Emperor (Apatura Iris).
  6. Larva of Duke of Burgundy Fritillary (Nemeobius Lucina).
  7. Pupa of Swallow-tail Butterfly (Papilio Machaon).
  8. Pupa of Orange Tip (Euchloë Cardamines).
  9. Pupa of Silver-washed Fritillary (Argynnis Paphia).
  10. Pupa of Purple Emperor (Apatura Iris).
  11. Pupa of Duke of Burgundy Fritillary (Nemeobius Lucina).
  12. Pupa of Dingy Skipper (Nisoniades Tages).

[Pg 350]

Plate IX

  1. Privet Hawk Moth (Sphinx Ligustri).
  2. Spurge Hawk (Deilephila Euphorbiæ).
  3. Large Elephant Hawk (Chœrocampa Elpenor).
  4. Eyed Hawk (Smerinthus Ocellatus).
  5. Lime Hawk (Smerinthus Tiliæ).
  6. Humming-bird Hawk (Macroglossa Stellatarum).
  7. Broad-bordered Five-spotted Burnet (Zygæna Trifolii).

Plate X

  1. Cinnabar Moth (Euchelia Jacobææ).
  2. Wood Tiger (Nemeophila Plantaginis).
  3. Tiger (Arctia Caia).
  4. Cream-spot Tiger (Arctia Villica).
  5. Oak Eggar (Bombyx Quercus). Male.
  6. Lappet (Lasiocampa Quercifolia).
  7. Kentish Glory (Endromis Versicolor). Male.
  8. Emperor Moth (Saturnia Pavonia). Male.
  9. Buff Tip (Phalera Bucephala).

Plate XI

  1. Large Yellow Underwing (Triphæna Pronuba).
  2. Marvel-du-jour (Agriopis Aprilina).
  3. Small Angle Shades (Euplexia Lucipara).
  4. Mother Shipton (Euclidia Mi).
  5. Clifden Nonpareil (Catocala Fraxini).
  6. Dark Crimson Underwing (Catocala Sponsa).

Plate XII

  1. Herald (Gonoptera Libatrix).
  2. Swallow-tail Moth (Uropteryx Sambucaria).
  3. Brimstone Moth (Rumia Luteolata).
  4. Scalloped Oak (Crocallis Elinguaria).
  5. Brindled Beauty (Biston Hirtaria).
  6. Waved Umber (Hemerophila Abruptaria).
  7. Maiden’s Blush (Zonosoma Punctaria).
  8. Mottled Umber (Hybernia Defoliaria).
  9. Treble Bar (Anaitis Plagiata).



Plate II.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate III.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate IV.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate V.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate VI.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate VII.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate VIII.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate IX.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate X.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate XI.

Danielsson & Co., del. ad. Nat. et Chromolith.




Plate XII.

Danielsson & Co., del. ad. Nat. et Chromolith.


[Pg 351]

INDEX

  • Bætica, 188
  • Bapta, 277
  • Basilinea, 247
  • Bath White, 146
  • Batis, 237
  • Beating for moths, 83
  • Beautiful Carpet, 286
  • Beautiful China Mark, 293
  • Bellargus, 191
  • Betulæ, 183
  • Betularia, 272
  • Bicolorata, 285
  • Bifida, 234
  • [Pg 352]Bilineata, 287
  • Binaria, 232
  • Biston, 271
  • Black Arches, 227
  • Black Hairstreak, 184
  • Black-veined White, 141
  • Blood Vein, 276
  • Blue-bordered Carpet, 285
  • Blue Chalk Hill, 192
  • —— Clifden, 191
  • —— Common, 190
  • —— Holly, 193
  • —— Large, 194
  • —— Mazarine, 193
  • —— Silver-studded, 189
  • —— Small, 194
  • —— Tailed, 188
  • Boarmia, 273
  • Boarmiidæ, 272
  • Bombyces, 217
  • Bombycidæ, 229
  • Bombycoidæ, 240
  • Bombyx, 229
  • Bordered White, 279
  • Botys, 293
  • Brassicæ (Pieris), 142
  • Brassicæ (Mamestra), 246
  • Bright-line Brown-eye, 260
  • Brimstone Butterfly, 152
  • Brimstone Moth, 269
  • Brindled Beauty, 271
  • Brindled Pug, 284
  • Broad-barred White, 257
  • —— bordered Bee Hawk, 211
  • —— —— Five spotted Burnet, 215
  • Brown Argus, 189
  • —— Hairstreak, 183
  • —— line Bright-eye, 242
  • —— Meadow, 178
  • —— Northern, 175
  • —— Tail, 226
  • Bryophila, 239
  • Bryophilidæ, 239
  • Bucephala, 236
  • Buff Ermine, 222
  • —— Tip, 236
  • Bullrush, 243
  • Bupalus, 279
  • Burnets, 215
  • Burnished Brass, 263
  • Butterflies—British, 139
  • —— antennæ of, 5
  • —— body, 3
  • —— catching, 64
  • —— eye, 3
  • —— legs, 8, 10
  • —— proboscis, 6
  • —— wings, 2, 8
  • Cabbage Moth, 246
  • Cabera, 277
  • Caberidæ, 276
  • Cabinets, 134
  • Caia, 221
  • Callimorpha, 220
  • C-Album, 164
  • Calymnia, 256
  • Camberwell Beauty, 167
  • Camelina, 235
  • Camptogramma, 287
  • Caradrina, 249
  • Caradrinidæ, 248
  • Cardamines, 148
  • Cardui, 169
  • Carpocapsa, 302
  • Carterocephalus, 201
  • Catching Butterflies, 64
  • —— moths, 82, 85
  • Caterpillar state, 22
  • Catocala, 265
  • Catocalidæ, 265
  • Cerastis, 256
  • Chalk-hill Blue, 192
  • Cheloniidæ, 220
  • Chequered Skipper, 201
  • Chestnut, 256
  • Chilo, 296
  • Chinese Character, 233
  • Chloroform bottle, 72
  • Chocolate Tip, 237
  • Chœrocampa, 207
  • Chrysalis state, 44
  • Chrysitis, 263
  • Chrysorrhœa, 226
  • Cidaria, 288
  • Cilix, 233
  • Cinnabar, 219
  • Cinxia, 162
  • Cirsiana, 301
  • Classification of Lepidoptera, 55
  • Clearwings, 212
  • Clifden Blue, 191
  • Clifden Nonpareil, 265
  • Clouded Silver, 277
  • Clouded Yellow, 151
  • Cœnonympha, 181
  • Coleophora, 305
  • Colias, 149
  • Collecting box, 73
  • Collecting larvæ, 101
  • —— ova, 99
  • —— pupæ, 108
  • Comes, 253
  • Comma, 164, 200
  • Common Blue, 190
  • [Pg 353]
    —— Carpet, 286
  • Common Emerald, 274
  • —— Footman, 219
  • —— Heath, 278
  • —— Quaker, 255
  • —— Swift, 223
  • —— Wainscot, 243
  • —— Wave, 277
  • Complanella, 306
  • Conigera, 242
  • Copper—Large, 187
  • —— Small, 188
  • Corydon, 192
  • Cosmiidæ, 256
  • Cossidæ, 224
  • Cossus, 224
  • Coxcomb Prominent, 235
  • Crambi, 296
  • Crambus, 297
  • Cratægi, 141
  • Cream-spot Tiger, 221
  • Cristana, 300
  • Crocallis, 270
  • Cucullatella, 218
  • Cucullia, 261
  • Cuprella, 304
  • Currant Clearwing, 213
  • Currant Moth, 279
  • Curtula, 237
  • Cyanide bottle, 68
  • Cymatophoridæ, 237
  • Daplidice, 146
  • Dark Crimson Underwing, 266
  • Dark Dagger, 241
  • Dark Green Fritillary, 158
  • Dark Hairstreak, 185
  • Death’s-head Hawk, 204
  • Decoys, 96
  • Defoliaria, 281
  • Deilephila, 207
  • Dentina, 259
  • Depressaria, 304
  • Dicranura, 234
  • Dicranuridæ, 233
  • Didymata, 283
  • Diloba, 241
  • Dilutata, 282
  • Dingy Skipper, 198
  • Dispar, 187, 227
  • Diurnea, 303
  • Dominula, 220
  • Dot, 247
  • Drepana, 232
  • Drepanulidæ, 232
  • Drinker, 230
  • Duke of Burgundy, 196
  • Dun-bar, 256
  • Fagella, 303
  • Farinalis, 292
  • Fidoniidæ, 278
  • Figure of Eight, 241
  • Filipendulæ, 215
  • Flame, 245
  • Flame Shoulder, 252
  • Flavago, 256
  • Flavicornis, 238
  • Flounced Rustic, 246
  • Fluctuata, 287
  • Forester, 214
  • Forficalis, 293
  • Fraxini, 265
  • Fritillaries, 154
  • Fritillary, Dark Green, 158
  • —— Glanville, 162
  • [Pg 354]
    —— Greasy, 161
  • —— Heath, 163
  • —— High Brown, 159
  • —— Pearl-bordered, 156
  • —— Queen of Spain, 156
  • —— Silver-washed, 159
  • —— Small Pearl-bordered, 154
  • Galatea, 173
  • Galleria, 298
  • Gamma, 264
  • Garden Carpet, 287
  • Garden Dart, 251
  • Garden Pebble, 293
  • Gemmaria, 273
  • Geoffrella, 305
  • Geometra, 274
  • Geometræ, 268
  • Geometridæ, 274
  • Ghost Swift, 223
  • Gipsy, 227
  • Glaucata, 233
  • Goat Moth, 224
  • Gonodactyla, 294
  • Gonoptera, 264
  • Gonopteridæ, 262
  • Gonopteryx, 152
  • Gortyna, 244
  • Gothic, 254
  • Grass Rivulet, 283
  • Grayling, 177
  • Grease, 127
  • Greasy Fritillary, 161
  • Green Hairstreak, 186
  • Green-chequered White, 146
  • Green Silver-lined, 217
  • Grizzled Skipper, 197
  • Grey Arches, 259
  • Grey Dagger, 240
  • Grossulariata, 279
  • Hadena, 259
  • Hadenidæ, 257
  • Hairstreak, Black, 184
  • —— Brown, 183
  • —— Dark, 185
  • —— Green, 186
  • —— Purple, 185
  • —— White-letter, 184
  • Halia, 278
  • Hamellus, 297
  • Harpella, 305
  • Hawk Moths, 204
  • Heart and Dart, 250
  • Heath, Large, 179
  • —— Moth, 278
  • Heath, Small, 181
  • —— Fritillary, 163
  • Hecatera, 257
  • Helice, 151
  • Hemerophila, 273
  • Hemithea, 274
  • Hepialidæ, 223
  • Hepialus, 223
  • Herald Moth, 262
  • Hesperia, 198
  • Hesperiidæ, 197
  • Hexadactyla, 295
  • High Brown Fritillary, 159
  • Hirtaria, 271
  • Holly Blue, 193
  • Hornet Clearwing of Osier, 213
  • Hornet Clearwing of Poplar, 213
  • Hortuellus, 297
  • Humming-bird Hawk, 210
  • Humuli, 223
  • Hyale, 149
  • Hybernia, 280
  • Hyberniidæ, 280
  • Hydrocampa, 293
  • Hylophila, 217
  • Hyperanthus, 180
  • Hyponomeuta, 304
  • Kentish Glory, 231
  • Killing bottle, 68
  • Killing box, 70
  • Labial palpi, 6
  • Lace Border, 275
  • Lappet, 230
  • Larentia, 283
  • Larentiidæ, 282
  • Large Blue, 194
  • Large Copper, 187
  • Large Elephant, 208
  • [Pg 355]
    Large Emerald, 274
  • Large Heath, 179
  • Large Skipper, 200
  • Large Tortoiseshell, 165
  • Large White, 142
  • Large Yellow Underwing, 253
  • Larvæ, 22
  • Larvæ Beating, 107
  • Larvæ, blowpipe for, 131
  • Larva boxes, 101
  • Larva cage, 115
  • Larvæ collecting, 101
  • Larvæ, glass for, 114
  • Larvæ rearing, 113
  • Lasiocampa, 230
  • Latona, 156
  • Laurel box, 70
  • Leaf Miners, 33, 303
  • Leaf Rollers, 33, 303
  • Lecheana, 300
  • Legs of Lepidoptera, 8, 10
  • Leioptilus, 295
  • Leopard Moth, 225
  • Lepidoptera—antennæ, 5
  • —— body, 3
  • —— classification of, 55
  • —— eggs of, 16
  • —— general characteristics, 1
  • —— legs of, 8, 10
  • —— metamorphoses, 14
  • —— proboscis, 6
  • —— wings, 2, 8
  • Lesser Broad Border, 252
  • Lesser Yellow Underwing, 253
  • Leucania, 242
  • Leucaniidæ, 242
  • Leucophasia, 149
  • Leucophæaria, 280
  • Libatrix, 262
  • Light Arches, 245
  • Light Emerald, 270
  • Light Traps, 87
  • Ligniperda, 224
  • Ligustri, 206
  • Lime Hawk, 210
  • Limenitis, 170
  • Limitata, 289
  • Lineola, 199
  • Liparidæ, 226
  • Lithosia, 218
  • Lithosiidæ, 219
  • Lithoxylea, 245
  • Lobophora, 285
  • Lobster Moth, 28
  • Lophopteryx, 235
  • Lubricipeda, 222
  • Lucina, 196
  • Lucipara, 258
  • Lulworth Skipper, 199
  • Luperina, 246
  • Lupulinus, 223
  • Luteolata, 269
  • Lycæna, 183, 188
  • Lycænidæ, 183
  • Macariidæ, 278
  • Machaon, 139
  • Macroglossa, 210
  • Maiden’s Blush, 275
  • Malvæ, 197
  • Mamestra, 246
  • Mania, 254
  • Marbled Beauty, 239
  • Marbled Minor, 248
  • Margaritaria, 270
  • Marsh Moth, 281
  • Marsh Ringlet, 181
  • Marvel-du-jour, 258
  • Maura, 254
  • Mazarine Blue, 193
  • Meadow Brown, 178
  • Meal Moth, 292
  • Megacephala, 241
  • Megæra, 177
  • Melanargia, 173
  • Melanthia, 285
  • Melitæa, 161
  • Mellonella, 298
  • Menthastri, 222
  • Meticulosa, 258
  • Metrocampa, 270
  • Mi, 264
  • Miana, 248
  • Micro-lepidoptera, 290
  • Minima, 194
  • Monacha, 227
  • Montanata, 286
  • Morpheus, 249
  • Mother-of-pearl, 293
  • Mother Shipton, 264
  • Moths, 203
  • —— antennæ of, 5
  • —— catching, 82
  • —— traps, 87
  • Mottled Rustic, 249
  • Mottled Umber, 281
  • Mundana, 218
  • Muslin Moth, 218
  • Queen of Spain, 156
  • Quercifolia, 230
  • Quercinaria, 271
  • Quercus (Bombyx), 229
  • Quercus (Thecla), 185
  • Salicella, 301
  • Sambucaria, 268
  • Saturnia, 231
  • Saturniidæ, 231
  • Satyridæ, 173
  • Satyrus, 177
  • Scalloped Oak, 270
  • Scarlet Tiger, 220
  • Sciaphila, 301
  • Segetum, 250
  • Selene, 154
  • Semele, 177
  • Semiargus, 193
  • Serena, 257
  • Sesia, 213
  • Sesiidæ, 212
  • Setting boards, 122
  • Shark, 261
  • Shears, 259
  • Short-cloaked, 218
  • Sibylla, 170
  • Silaceata, 288
  • Silver-ground Carpet, 286
  • Silver-spotted Skipper, 200
  • Silver-studded Blue, 189
  • Silver-washed Fritillary, 159
  • Silver Y, 264
  • Sinapis, 149
  • Six-spot Burnet, 215
  • Skippers, 196
  • Skipper, Chequered, 201
  • —— Dingy, 198
  • —— Grizzled, 197
  • —— Lulworth, 199
  • —— New Small, 199
  • —— Silver-spotted, 200
  • —— Small, 198
  • Sleeving, 116
  • Small Angle Shades, 258
  • —— Blue, 194
  • —— Copper, 188
  • —— Elephant, 207
  • —— Heath, 181
  • —— Magpie, 292
  • —— Mallow, 289
  • —— Pearl-bordered Fritillary, 154
  • —— Phœnix, 288
  • —— Ringlet, 174
  • —— Seraphim, 285
  • —— Skipper, 198
  • —— Tortoiseshell, 166
  • —— White, 144
  • Smerinthus, 208
  • Smoky Wainscot, 243
  • Sociata, 286
  • Speckled Wood, 175
  • Sphinges, 203
  • Sphingidæ, 204
  • Sphinx, 206
  • Spilosoma, 222
  • Sponsa, 266
  • Spring Usher, 280
  • Spurge Hawk, 207
  • Stabilis, 255
  • Stagnata, 293
  • Statices, 214
  • Stellatarum, 210
  • Store boxes, 135
  • Strigata, 274
  • Strigilis, 248
  • Stuffing insects, 126
  • Sugaring, 92
  • Sugaring net, 94
  • Sugar traps, 96
  • Swallow-tail Butterfly, 139
  • Swallow-tail Moth, 268
  • Swifts, 223
  • Sylvanus, 200
  • Syrichthus, 197
  • W album, 184
  • Wainscots, 243
  • Wall Butterfly, 177
  • Waved Umber, 273
  • White Admiral, 170
  • —— Bath, 146
  • —— Black-veined, 141
  • —— Ermine, 222
  • —— Green-chequered, 146
  • —— Green-veined, 145
  • —— Large, 142
  • White-letter Hairstreak, 184
  • —— Marbled, 173
  • —— Small, 144
  • —— Wood, 149
  • Willow Beauty, 273
  • Wings, 2, 8
  • Wood Argus, 175
  • Wood Tiger, 220
  • Wood White, 149
  • Yellow-horned, 238
  • Yellow Shell, 287

PRINTED BY
SPOTTISWOODE AND CO., NEW-STREET SQUARE
LONDON

Transcriber’s Note

Some minor changes have been made to obvious format and punctuation
inconsistencies. Other inconsistent usages have been retained except
where obvious typographical errors have been corrected as follows:

Page vii ’40’ changed to ’44’ (IV. The Pupa or Chrysalis 44)

Page 97 ‘dicover’ changed to ‘discover’ (… not being able to discover the ‘entrance out,’ …)

Page 188 ‘Polyommatas’ changed to ‘Polyommatus’ (The Small Copper (Polyommatus Phlæas))

Page 219 ‘Jacobæa’ changed to ‘Jacobææ’ (Fig. 112.—The Larva of Jacobææ.)

Page 263 ‘rested’ changed to ‘crested’ (The abdomen also is crested, …)

Page 334 ‘Rannock’ changed to ‘Rannoch’ (Rannoch Geometer (Brunneata))

Page 354 ‘Ibipenella’ change to ‘Ibipennella’ (Ibipennella, 305)

Page 354 missing page reference added (Ichneumon flies, 25)

Page 355 ‘Leucophearia’ changed to ‘Leucophæaria’ (Leucophæaria, 280)

Page 356 ‘Octomacularia’ changed to ‘Octomaculana’ (Octomaculana, 301)

Page 358 ‘Tryphæna’ changed to ‘Triphæna’ and moved to its alphabetical position in the index (Triphæna, 252)

Page 358 ‘Umbricata’ changed to ‘Umbratica’ (Umbratica, 261)

 

 


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