CHAPTER XI.

THE COLOURATION OF INSECTS.

(_Continued._)

_General Scheme of Colouring._ So various are the patterns displayed

upon the wings of butterflies, that amidst the lines, stripes, bars,

dots, spots, ocelli, scalloppings, etc., it seems at first hopeless to

detect any general underlying principle of decoration; and this is the

opinion that has been, and is still, held by many who have made these

insects a special study. Nevertheless, we will try to show that beneath

this almost confused complexity lie certain broad principles, or laws,

and that these are expressed by the statement that decoration is

primarily dependent upon structure, dependent upon the laws of emphasis

and repetition, and modified by the necessity for protection or

distinction.

To render this subject as plain as possible, British species will be

selected, as far as possible, and foreign ones only used when native

forms do not suffice.

The body of by far the greater number of species is either darker or of

the same tint as the mass of the wings; and only in rare cases lighter.

When the body has different tints, it is generally found that the thorax

and abdomen differ in colour, and in many cases the base of the thorax

is emphasized by a dark or light band.

On the wings the functional importance of the parts attached to the body

is generally darker, perhaps never lighter, than the ground of the wing,

and is frequently further emphasized by silky hairs. This has already

been sufficiently pointed out.

The wing area may be divided into the strong costal margin, the hind

margin, the nervules, and the spaces; and, however complex the pattern

may be, it is always based upon these structure lines.

In the majority of insects the costal margin is marked with strong

colour. This may be noticed in _Papilio Machaon_, _P. merope_, _Vanessa

antiopa_, and the whites in Plate IV. The extreme tip of the fore-wings

is nearly always marked with colour, though this may run into the border

pattern. This colour is dark or vividly bright, and we know no

butterfly, not even dark ones, that has a light tip to the wings.

Sometimes, it is true, the light bead-border spots run to the tip, but

these are not cases in point. The development of tips has been traced in

Chapter VI., and need not be repeated.

The hind margin of both wings is very commonly emphasized by a border,

of which _V. Antiopa_, Pl. III. Fig. 3, is a very perfect example.

The border pattern may consist of one or more rows of spots, lines,

bands, or scallops;[31] and there is frequently a fine fringe, which in

many cases is white, with black marks, and to which the term

bead-pattern may be applied.

A definite relation subsists in most cases between the shape of the hind

margin and the character of the border-pattern. The plain or simple

bordered wings have plain border patterns, and the scalloped wings have

scalloped borders; or rather scalloped borders are almost exclusively

confined to scalloped wings. In our English butterflies, for instance,

out of the 62 species:--

33 have plain margins to the wings. In all the border is plain, or

wanting.

20 have the fore-wings plain, and the hind-wings scalloped, and in

all the hind-wings are scalloped and the fore-wings plain, or with

slightly scalloped border-patterns.

9 have scalloped margins and scalloped border-patterns.

Another relation between structure and pattern is found in those insects

which have tailed hind-wings, for the tail is very frequently emphasized

by a spot, often of a different colour from the rest of the wing as in

the Swallow-Tails, Plates IV. and V.

Yet another point may be noticed. In each wing there is a space, the

discoidal cell, _j_ Fig. 3, at the apex of which several nervures join,

forming knots. These are points at which obstacles exist to the flow of

the contents, and they are almost always marked by a distinct pattern.

We thus have a discoidal spot in very many butterflies, in nearly all

moths; and in the other orders of winged insects the decoration is even

more pronounced, as any one may see who looks at our dragon-flies,

wasps, bees, or even beetles.

In some insects the decoration of the body is very marked, as in our

small dragon-flies, the Agrions. In one species, for example, _A.

Puella_, the male is pale blue banded with black, and the female bronze

black, with a blue band on the segment, bearing the sexual organ; the

ovipositors are also separately decorated. The male generative organs

are peculiar, in that the fertilizing fluid is conveyed from one segment

to a reservoir at the other end of the abdomen. Both the segments

bearing these organs are marked by special decoration. The peculiar

arrangement of the sexual organs in dragon-flies is very variable, and

certain segments are modified or suppressed in some forms, as was shown

by J. W. Fuller.[32] In every case the decoration follows the

modification. In the thorax of dragon-flies, too, the principal muscular

bands are marked out in black lines. This distinct representation of the

internal structure is beautifully shown in _Æschna_ and _Gomphina_, and

in the thorax of _Cicada_, as shown by Dr. Haagen in the paper quoted in

the last chapter.

We may, then, safely pronounce that the decoration of insects is

eminently structural.

_Simple Variation._ Cases of simple variation have been already cited in

our description of spots and stripes, and it only remains to show that

in this, as in all other cases, the variation is due to a modification

of original structural decoration.

To take familiar examples. Newman, in his British Butterflies, figures

the varieties of the very common Small Tortoiseshell (_Vanessa urticæ_).

In the normal form there is a conspicuous white spot on the disc of the

fore-wings, which is absent in the first variety, owing to the spreading

of the red-brown ground colour. This variety is permanent on the

Mediterranean shores. In variety two, the second black band, running

from the costa across the cell, is continued across the wing. The third

variety, Mr. Newman remarks, is "altogether abnormal, the form and

colouring being entirely altered." Still, when we examine the insect

closely, we find it is only a modification of the original form. The

first striking difference is in the margin of the wings, which in the

normal form is scalloped with scallop-markings, whereas, in the variety

the margins are much simpler, and the border pattern closely corresponds

with it, having lost its scalloping. In the fore-wing some of the black

bands and spots are suppressed or extended, and the extensions end

rigidly at nervules. The dark colouring of the hind-wings has spread

over the whole wing. We thus see that the decoration, even in varieties

called abnormal, still holds to structural lines, and is a development

of pre-existing patterns.

No one can have examined large series of any species without being

impressed with the modification of patterns in almost every possible

way. For instance, we have reared quantities of _Papilio Machaon_, and

find great differences, not only in the pattern, but in the colour

itself. A number of pupæ from Wicken Fen, Cambridgeshire, were placed in

cages, into which only coloured light could fall, and though these

experiments are not sufficiently extended to allow us to form any sound

conclusions as to the effect of the coloured light, we got more

varieties than could be expected from a batch of pupæ from the same

locality. The tone of the yellow, the quantity of red, the proportion of

the yellow to the blue scales in the clouds, varied considerably, but

always along the known and established lines.

The variations in the colour of Lepidoptera has been most admirably

treated by Mr. J. Jenner Weir in a paper, only too short, read before

the West Kent Natural History Society.[33] He divides variations into

two sections, Aberrations or Heteromorphism, and constant variations or

Orthopæcilism, and subdivides each into six classes, as under:--

_Heteromorphism._

Albinism ... ... white varieties.

Melanism ... ... black do.

Xanthism ... ... pallid do.

Sports ... ... or occasional variations not included

in the above.

Gynandrochomism ... females coloured as males.

Hermaphroditism ... sexes united.

_Orthopæcilism._

Polymorphism ... variable species.

Topomorphism ... local varieties.

Atavism ... ... reversion to older forms.

Dimorphism ... ... two constant forms.

Trimorphism ... ... three do. do.

Horeomorphism ... seasonal variation.

In some cases, he remarks, variations are met with which may with equal

propriety be classed in either section.

Albinism he finds to be very rare in British species, the only locality

known to him being the Outer Hebrides. This reminds us of Wallace's

remark upon the tendency to albinism in islands. Xanthism, he finds to

be more plentiful, and quotes the common Small Heath (_Cænonympha

pamphilus_) as an illustration. In these varieties we have simply a

bleaching of the colouring matter of the wings, and therefore no

departure from structural lines. Melanism arises from the spreading of

large black spots or bars, or, as in _Biston betularia_, a white moth

peppered with black, dots by the confluence of small spots; for this

insect in the north is sometimes entirely black. It is singular that

insects have a tendency to become melanic in northern and alpine places,

and this is especially the case with white or light coloured species.

(_See_ Plate IV., Fig. 17) It has recently been suggested that this

darkening of these delicate membranous beings in cold regions is for the

purpose of absorbing heat, and this seems very probable.[34]

Of ordinary spots it is merely necessary to remark, that they are all

cases in our favour. Thus, in _Satyrus hyperanthus_ we have "the

ordinary round spots ... changed into lanceolate markings"; this takes

place also in _C. davus_. The other cases of aberration do not concern

us.

When, however, we come to the cases in which a species has two or more

permanent forms, it is necessary to show that they are in all cases

founded on structure lines. The patterns, as shown in Plate V., Figs.

1-13, are always arranged structurally, and the fact that not only are

intermediate forms known, as in _Araschnia porima_, Plate V., Fig. 6,

but that the various forms are convertible into one another, would in

itself be sufficient to show that in these cases there is no departure

from the general law. In _Grapta interrogationis_, Plate V., Figs. 8-10,

we see in the central figure one large spot above the median nervure, in

the left-hand form this is surmounted by another spot above the lowest

sub-costal branch, and in the right-hand figure this latter spot is very

indistinct. We have here a perfect gradation, and the same may be said

of the colouration of the lower wings. Take again the three forms of

_Papilio Ajax_ in the same plate, Figs. 11-13, and we have again only

modifications of the same type.

In local varieties, as in seasonal forms, we have again nothing more

than developments of a given type, as is well shown in Plates IV. & V.,

Figs. 13-18 & 1-13.

When, however, we come to mimetic forms, whether they mimic plants, as

in Plate I., or other species, as in Plates II. & III., a difficulty

does seem to arise.

The leaf butterfly (_Kallima inachus_), Plate I., offers no trouble when

we view the upper surface only with its orange bands, but its under

surface, so marvellously like a dead leaf that even holes and

microscopic fungi are suggested, does seem very like a case in which

structure lines are ignored. Take, for instance, the mark which

corresponds to the mid-ribs, running from the tail to the apex of the

upper wing; it does not correspond to any structure line of the insect.

But if we take allied and even very different species and genera of

Indian and Malayan butterflies, we shall find every possible

intermediate form between this perfect mimicry and a total lack of such

characters. To cite the most recent authority, the various species of

the Genera Discophora, Amathusia, Zeuxidia, Thaumantis, Precis, &c.,

figured so accurately in Distant's Rhopalocera Malayana, will give all

the steps.

In the cases of true mimicry, as in Figs. 1-3, Plates II. & III., where

insects as different as sheep from cats copy one another, we find that

of course structure lines are followed, though the pattern is vastly

changed. The _Papilio merope_, Fig. 1, Plate II., which mimics _Danais

niavius_, Fig. 3, does so by suppressing the tail appendage, changing

the creamy yellow to white--a very easy change, constantly seen in our

own Pieridæ--and diffusing the black. A similar case is seen in Figs.

4-5, Plate III., where a normally white butterfly (_Panopoea hirta_)

mimics a normally dark one of quite a different section. Here again the

change is not beyond our power of explanation. Where a Papilio like

_merope_ mimics a brown species like _Danais niavius_, we have a still

greater change in colour, but not in structural pattern.

If we ascribe to these insects the small dose of intelligence we believe

them to possess, we can readily see how the sense of need has developed

such forms.

Local varieties present no difficulty under such explanation. The

paramount necessity for protection has given the Hebridran species the

grey colour of the rocks, and the desert species their sandy hue.

[Illustration: Plate VII.

CATERPILLARS.]

Finally, to take the case of caterpillars, Weismann has admirably worked

out the life history of many forms, and shows how the complex markings

have arisen by development. Broadly, a caterpillar consists of 13

segments, the head being one. The head is often marked with darker

colour, and the last segment with its clasping feet is also very

frequently emphasized, as in Figs. 1 & 3, Plate VII. The spiracles are

generally marked by a series of spots, and often connected by a line.

Here the tendency to repetition shows itself strongly, for not only the

spiracles themselves, but the corresponding points in the segments

without spiracles are frequently spotted, and, moreover, these spots are

frequently repeated in rows above the spiracular line. Of this,

_Deilephila galii_ and _D. Euphorbiæ_, Figs. 1-5, Plate VII., are good

examples.

The segmentation is also generally emphasized, as shown in all the

examples on the plate, but in its simplicity in Fig. 10.

Running down the centre of the back a more or less distinct line is

often seen, as shown in the figures. This corresponds with the great

dorsal alimentary canal lying just below the skin, and Weismann has

shown that in young larvæ this line is transparent, and the green food

can be seen through the skin. We have here, perhaps, a relic of the

direct colouration noticed in the transparent coelenterata.

Where larvæ possess horns either upon the head, as in _Apatura iris_ and

_Papilio machaon_, or on the tail, as in many of the sphyngidæ, like

Figs. 1-5, Plate VII., these appendages are always emphasized in colour.

As they are frequently oblique, we often find that this obliquity is

continued as a slanting spot, as in _D. galii_ and _euphorbiæ_, and

sometimes repeated as a series of oblique stripes, as in Fig. 4.

It must be admitted that in insects we have strong evidence of

structural decoration.

[Illustration]

[31] In the true scallop pattern the convexity is turned towards the

body of the insect.

[32] J. W. Fuller on the Breathing Apparatus of Aquatic Larvæ. Proc.

Bristol Nat. Soc.

[33] Entomologist, vol. xvi., p. 169, 1883.

[34] Nature. R. Meldola on Melanism, 1885.

CHAPTER XII.

ARACHNIDA.

The Arachnida include the scorpions and spiders, and as the former are

tolerably uniform in colour, our remarks will be confined to the latter.

The thorax is covered with a horny plate, while the abdomen only

possesses a soft skin, and neither show any traces of segmentation. From

the thorax spring four pairs of legs, and a pair of palpi, or feelers.

Immediately beneath the skin of the abdomen lies the great dorsal

vessel, which serves as a heart. This vessel is divided into three

chambers, the general aspect of which is shown in Fig. 9, Plate VIII.,

taken from Gegenbaur's Comparative Anatomy.[35]

From this heart the blood passes by vessels to each of the limbs, the

palpi, etc., as offsets from the double-branched aorta. The shape of

this dorsal vessel is peculiar, and its importance in respect to

colouration will be immediately apparent.

The primary scheme of colouration in the Arachnida seems to be the

distinguishing of the cephalothorax from the abdomen by a different

colour. Thus, of the 272 species of British spiders represented in

Blackwell's work,[36] no less than 203 have these parts differently

coloured, and only 69 are of the same hue, and even in these there is

often a difference of tint. So marked is this in certain cases that the

two parts form vivid contrasts. Of this cases are given in the following

list.

Cephalothorax. Abdomen.

_Eresus cinnabarinus_, Black, Bright Red.

_Thomisus floricolens_, Green, Brown.

---- _cinereus_, Brown, Blue.

---- _trux_, Red, Brown.

_Sparassus smaragdulus_, Green, Red and yellow.

As a rule the abdomen is darker than the cephalothorax, and many species

have the former red-brown and the latter black.

The legs, usually, take the colour of the cephalothorax, and are, hence,

generally lighter than the abdomen, but to this there are exceptions.

Where the individual legs differ in colour, the two first pairs are the

darkest, and the dark hue corresponds in tint with the dark markings on

the cephalothorax. The joints of the legs are in many species emphasized

with dark colour, which is often repeated in bands along the limb.

The most remarkable point is, however, the pattern on the abdomen,

which, though varied in all possible ways, always preserves a general

character, so that we might speak with propriety of a spider-back

pattern. This pattern is fairly well illustrated in the genus _Lycosa_,

but is seen to perfection, and in its simplest form in _Segestria

senoculata_, Plate VIII., Fig. 1, and in _Sparassus smaragdulus_, Plate

VIII., Fig. 2.

This peculiar pattern is so like the dorsal-vessel that lies just

beneath, that it is difficult to avoid the conclusion that we have here

an actual case of the influence of internal organs on the integument,

and this we believe to be the case. No matter how curious the abdominal

markings may seem to be, they never so far depart from this fundamental

pattern as to appear independent of it.

Thus, in the genus _Lycosa_, which is by no means the best for the

purpose, but is chosen as illustrating Gegenbaur's diagram, Pl. VIII.,

we have the dorsal-vessel well marked in _L. piscatoria_, Plate VIII.,

Fig. 3, from which may be developed the other forms. In _L.

andrenivora_, Plate VIII., Fig. 4, the male shows the vessel-mark

attenuated posteriorly; and in the female, Fig. 5, the hinder part has

become broken up into detached marks, still preserving the original

shape, while the upper part remains practically unchanged. In _L.

allodroma_ the disintegration of the mark has further advanced, for in

the male, Fig. 6, the upper portion has lost something of its shape, and

the lower part is a series of isolated segments. This process is carried

still further in the female, Fig. 8, where the upper portion is

simplified, and the lower almost gone. In _L. campestris_, Fig. 10, the

mark is reduced to a stripe, corresponding with the upper part of the

vessel-mark only: and, lastly, in the male _L. agretyca_, Fig. 7, this

upper part is represented by two spots, though even here traces of the

original form can be seen.

A simplification of marking of another sort is seen in _L. rapax_, Fig.

13, where the chamber-markings are almost obliterated, and merely an

irregular stripe left. The stages by which this modification is arrived

at are too obvious to need illustration.

In some species the lower portion of the vessel-mark is reduced to small

dots, as in _L. cambrica_, _fluviatilis_, _piratica_, and others; and

the stages are very clear. Starting with the isolated chamber-marks, as

in _L. allodroma_, Fig. 5, we get, firstly, a set of spots, as in _L.

picta_, which, in the female, Fig. 16, are still connected with the

chamber-marks, but in the male, Fig. 17, are isolated. This leads us, by

easy steps, to such forms as _L. latitans_, Fig. 14, which consists of a

double row of spots upon dark stripes.

The intimate connection thus shown to subsist between the characteristic

decoration of the abdomen of spiders, and the shape of the important

dorsal organ beneath, seems to be strong evidence of effect that

internal structure may have upon external decoration.[37]

The cephalothorax of spiders, being covered with a hardened membrane,

does not show such evidence clearly, for it appears to be a law that the

harder the covering tissue, the less does it reflect, as it were, the

internal organs. The hard plates of the armadillo are thus in strong

contrast to the softer skins of other animals.

Nevertheless, there does appear, occasionally, to be some trace of this

kind of decoration in the cephalothorax of certain spiders, though it

would be hard to prove. The blood vessels of this part (see Fig. 9),

though large, are not nearly so prominent as the great dorsal vessel.

The chief artery enters the cephalothorax as a straight tube, forks, and

sends branches to the limbs, palpi, and eyes. In many species, notably

in the genus _Thomisus_, a furcate mark seems to shadow the forked

aorta. This is best shown in _T. luctuosus_, Plate VIII., Fig. 11.

Moreover, in this and other genera, lines frequently run to the outer

pair of eyes, which alone are supplied with large arteries, see Fig. 9.

However this may be, it is certain that the entire decoration of spiders

follows structural lines, and that the great dorsal vessel has been

emphasized by the peculiar pattern of the abdomen.

[Illustration: Plate VIII.

SPIDERS.]

[35] Elements of Comparative Anatomy, by C. Gegenbaur. Translated by

Jeffrey Bell and Ray Lankester, 1878, p. 285.

[36] Spiders of Great Britain and Ireland, J. Blackwell. Ray. Soc.,

1861.

[37] The decoration of many of the Hoverer flies and wasps is of a

similar character.

CHAPTER XIII.

COLOURATION OF INVERTEBRATA

(_Continued_).

Of the Arthropoda, including the lobsters, crabs, shrimps, etc., little

can be said here, as we have not yet been able to study them with

anything like completeness. Still, we find the same laws to hold good.

The animals are segmented, and we find their system of colouration

segmental also. Thus, in the lobsters and crabs there is no dorsal line,

but the segments are separately and definitely decorated. The various

organs, such as the antennæ and eyes, are picked out in colour, as may

be beautifully seen in some prawns.

When we come to the Mollusca, we meet with two distinct types, so far as

our subject is concerned; the naked and the shelled. In the naked

molluscs, like the slugs, we have decoration applied regionally, as is

shown to perfection in the _Nudibranchs_, whose feathery gills are often

the seat of some of the most vivid hues in nature.

The shell-bearing mollusca are proverbial for their beauty, but it is

essential to bear in mind that the shell does not bear the same relation

to the mollusc that the "shell" of a lobster does to that animal. The

lobster's shell is part of its living body; it is a true exo-skeleton,

whereas the shell of a mollusc is a more extraneous structure--a house

built by the creature. We ought, on our view, to find no more relation

between the decoration of a shell and the structure of its occupant,

than we do in the decoration of a human dwelling-house to the tenant.

The shell consists of carbonate of lime, under one or both of the forms

known to mineralogists as calcite and aragonite. This mineral matter is

secreted by an organ called the mantle, and the edge, or lip, of the

mantle is the part applied to this purpose. The edge of the mantle is

the builder's hand, which lays the calcareous stones of the edifice.

The shell is built up from the edge, and the action is not continuous

but seasonal, hence arise the markings known as lines of growth. In some

cases the mantle is expanded at times into wing-like processes, which

are turned back over the shell, and deposit additional layers, thus

thickening the shell.

In all the forms of life hitherto considered the colouring matter is

deposited, or formed, in the substance of the organ, or epidermal

covering, but in the mollusca this is not the case. The colouring matter

is entirely upon the surface, and is, as it were, stencilled on to the

colourless shell. This is precisely analogous to the colouring of the

shells of birds' eggs. They, too, are calcareous envelopes, and the

colouring matter is applied to the outside, as anyone can see by rubbing

a coloured egg. In some eggs several layers of colouring matter are

superimposed.

In no case does the external decoration of molluscan shells follow the

structure lines of the animal, but it does follow the shape of the

mantle. The secreting edge may be smooth, as in _Mactra_, regularly

puckered, as in most _Pectens_, puckered at certain points, as in

_Trigonia_, or thrown into long folds, as in _Spondylus_. In each of

these cases the shell naturally takes the form of the mantle. It is

smooth in _Mactra_, regularly ribbed in _Pecten_, tubercled in

_Trigonia_, and spined in _Spondylus_. Where the inside of the shell is

coloured as in some Pectens, regional decoration at once appears and the

paleal lines, and muscular impressions are bounded or mapped out with

colour.

It is a significant fact that smooth bivalves are not so ornate as

rugose ones, and that the ridges, spines, and tubercles of the latter

are the seats of the most prominent colour.

Similar remarks apply to univalve shells, which are wound on an

imaginary vertical axis. They may be smooth, as in _Conus_ and _Oliva_,

rugose, as in _Cerithium_, or spined, as in _Murex_. The structure of

these shells being more complex than that of bivalves, we find, as a

rule, they are more lavishly ornamented, and the prominent parts of the

shell, and especially the borders, are the seat of strongest colour. In

some cases, as in adult Cowries (_Cypræa_), the mantle is reflexed so as

to meet along the median line, where we see the darkest colour.

The rule amongst spiral shells is to possess spiral and marginal

decoration, and this is what we should expect. The Nautilus repeats in

the red-brown markings of its shell, the shape of the septa which

divide the chambers, though, as is often the case, they are generally

more numerous than the septa.

The naked Cephalopoda, or cuttle-fishes, often possess a distinct dorsal

stripe, and when our views were first brought before the Zoological

Society, this fact was cited as an objection. To us it seems one of the

strongest of favourable cases, for these animals possess a sort of

backbone--the well-known cuttle-bone--and hence they have a dorsal line.

Some shells, as _Margarita catenata_, have a chain-pattern, and in this

case the action of the pigment cells takes place at regular and short

intervals. Others, as _Mactra stultorum_, the stencilling forms a series

of lines and spots, generally enlarging into rays.

The whole subject of the decoration of shells deserves much more time

than we have been able to give to it as yet.

[Illustration]

CHAPTER XIV.

COLOURATION OF VERTEBRATA.

The vertebrata, as their name implies, are distinguished by the

possession of an internal skeleton, of which the backbone is the most

essential part, and the general, but not universal, possession of limbs

or appendages.

Consequently we find that the dorsal and ventral surfaces are almost

invariably coloured differently, and the dorsal is the darker in the

great majority of instances. Generally the spine is marked by a more or

less defined central line, and hence this system of colouration may be

termed axial, because it is in the direction of the axes, or applied

about the axes.

_Fishes._ Where fishes have not been modified out of their original

form, as are the soles, plaice, and other flat fish, we find the dorsal

region darker than the ventral, and even here the under surfaces are the

lightest. Even in cases like the Char, Fig. 1, Plate IX., where vivid

colour is applied to the abdomen, the dorsum is the darker. The dorsum

is often marked by a more or less well-defined dark band, as in the

mackerel and perch, Fig. 2, Plate IX. There are sometimes parallel bands

at right angles to the above, as in the perch and mackerel; and this is

a common feature, and apparently a very old one, as we find it in the

young of fishes whose adults are without these rib-like marks, such as

the trout and pike.

It is only necessary to inspect any drawings of fishes to see that their

colouration is on a definite principle, although rather erratic.

Important functional parts, like the gills, fins, and tail, are

generally marked in colour more or less distinctly, as may be seen, for

instance, in our common fresh-water fishes, like the roach and perch.

The line of mucus-secreting glands running along the sides is usually

marked by a dark line. These facts point distinctly to structural

decoration.

[Illustration: Plate IX.

CHAR AND PERCH.]

There are in some fishes, like the John Dory, curious eye-like dark

spots, which we cannot refer to a structural origin, though a better

acquaintance with the class might reveal such significance.

The Amphibia have not been well studied by us, and we must leave them

with the remark that they seem to bear out the view of structural

decoration, as is seen in our English newts. Some are, however, modified

out of all easy recognition.

_Reptiles._ Among the reptiles, the snakes, Fig. 4, may be selected for

illustration. Snakes are practically little more than elongated

backbones, and are peculiar from the absence of limbs. The colouring

matter does not reside so much in the scales as in the skin beneath, so

that the sloughs do not illustrate the decoration. Hence, we might

expect to find here a direct effect of morphological emphasis.

The ornamentation of snakes is very similar throughout the class, both

in water and land snakes; as may be seen by Sir W. Fayrer's work on

Venomous Snakes. This ornamentation is of a vertebral pattern, placed

along the dorsal surface, with cross lines, which may represent ribs.

Where the ribs are wanting, as in the neck, the pattern changes, and we

get merely longitudinal markings.

In the Python, Fig. 4, there are, near the central line, numerous round

spots, which apparently emphasize the neural processes. There are

diagonal markings on some species which illustrate the development of

colour-spots already alluded to.

This snake-pattern is very singular and striking. The markings are fewer

in number than the vertebræ, yet their true vertebral character is most

obvious.

In Snakes, again, we find the dorsal region is darker than the ventral.

In the Lizards there are patches of colour placed axially, while each

patch covers a number of scales.

_Birds._ Birds have their whole economy modified to subserve their great

functional peculiarity of flight.

Immense muscles are required for the downward stroke of the wing, and to

give attachment to these the sternum has a strongly developed keel. To

bring the centre of gravity low, even the muscles which raise the wing

are attached to the sternum, or breastbone, instead of to the dorsal

region, as might be expected; and to brace the wings back a strong

furculum--the merry-thought--is attached. The breast, then, is the seat

of the greatest functional activity in birds, and, consequently, we find

in a vast number of birds that the breast is the seat of vivid colour.

As many birds are modified for protective purposes, the brightest

species were selected to test our views, namely, the Birds of Paradise

(Paradisea), Humming Birds (Trochilidæ), and Sun Birds (Nectarinidæ). In

these birds it is clear that colour has had full sway, untramelled by

any necessity for modification.

Nothing is more striking than the mapping out of the surface of these

birds into regions of colour, and these regions are always bounded by

structural lines.

Take, for instance, _Paradisea regia_. In this bird we find the

following regions mapped in colour:--

Sternum brown.

Clavicle yellow.

Pelvis yellow.

Band brown.

Frontal bone black.

Parietal bones green.

Occiput yellow.

A beautiful ruff emphasizes the pectoral muscles, and the tail

appendages emphasize the share-like caudal vertebræ.

If we turn to the other species of this genus, we find in _P. Papuana_

the claret breast suddenly change to green at the furculum; and similar

changes take place in _P. speciosa_, while in _P. Wallacei_ and

_Wilsoni_ this region is decorated with a wonderful apron of metallic

green.

The region of the furculum is equally well marked in the Toucans and

Sun-birds.

If now we observe the back of a bird, and view the skeleton with the

wings at rest, we shall find it falls into three morphological tracts.

First, the shoulder, or scapular track; second, the thigh, or pelvic;

third, the tail, or caudal region; and in all these birds the several

tracts are beautifully marked by sudden and contrasted change of colour.

In _P. Wilsoni_ all the tracts are brilliant red, but they are separated

by jet-black borders. In _Nectarinea chloropygia_ the scapular region is

red, the pelvic yellow, and the caudal green.

[Illustration: Plate X.

SUN BIRDS.]

In _P. Wilsoni_ we have a wonderful example of morphological emphasis.

The head is bare of feathers, and coloured blue, except along the

sutures of the skull, where lines of tiny black feathers map out the

various bones.

But morphological emphasis exists everywhere in birds. The

wing-primaries, which attach to the hand, are frequently differently

decorated from the secondaries, which feathers spring from the ulna; and

the spur-feathers of the thumb, or pollux, are different in shape, and

often in colour, from the others, as every fly-fisher who has used

woodcock spur-feathers knows full well. The wing-coverts and

tail-coverts are frequently mapped in colour; and the brain case is

marked by coloured crests. The eye and ear are marked by lines and

stripes; and so we might go on throughout the whole bird. We may remark

that these very tracts are most valuable for the description and

detection of species, and among ornithologists receive special names.

Now, this distribution of colour is the more remarkable inasmuch as the

feathers which cover the surface--the contour feathers--are not evenly

distributed over the body, but are confined to certain limited tracts,

as shown by Nitzsch; and though these tracts have a morphological

origin, they are rendered quite subsidiary to the colouration, which

affects the whole bird, and not these regions in particular. In fact,

the colouration is dependent upon the regions on which the feathers lie,

and not upon the area from which they spring. In other words, we seem to

have in birds evidence of the direct action of underlying parts upon the

surface.

In more obscurely coloured birds, and those which seem to be evenly

spotted, close examination shows that even here the decoration is not

uniform, but the sizes and axes of the spots change slightly as they

occupy different regions; as may be seen in Woodpeckers and Guinea-fowl.

Although the same tone of colour may prevail throughout the plumage, as

in the Argus Pheasant, great variety is obtained by the fusion of spots

into stripes. A symmetrical effect is produced by the grouping of

unsymmetrical feathers; as is so often seen in plants, where irregular

branches and leaves produce a regular contour.

Sometimes, especially on the breast and back, the feathers of one region

seem to unite so as to form one tract, so far as colour is concerned.

Thus, if in _P. Wilsoni_ the black borders of the dorsal regions were

suppressed, all three areas would be of one hue. This seems to have

been the case in the breast region of Humming Birds, where only the

throat is highly coloured. In the Toucans the breast and throat regions

are often marked with colour; but sometimes the hue is the same and the

boundaries of the regions marked with a band of another colour; if this

boundary band be increased, the regions do not seem so well shown, for

the boundary becomes as broad as the area; yet, in all these cases the

dependence upon regional decoration is manifest. No doubt the few

uniformly coloured birds were derived from species which were once

variously hued; the gradation of colour being lost in transmission.

_Mammalia._ The axial decoration of the mammalia is very definite, and

nearly all species have a dorsal tract marked with colour. The dark

bands on the back of the horse, ox, and ass, are cases in point. In

nearly every case the dorsal is darker than the ventral surface.

If we take highly decorated species, that is, animals marked by

alternate dark and light bands, or spots, such as the zebra, some deer,

or the carnivora, we find, first, that the region of the spinal column

is marked by a dark stripe (Figs. 9 & 16); secondly, that the regions of

the appendages, or limbs, are differently marked; thirdly, that the

flanks are striped, or spotted, along or between the regions of the

lines of the ribs; fourthly, that the shoulder and hip regions are

marked by curved lines; fifthly, that the pattern changes, and the

direction of the lines, or spots, at the head, neck, and every joint of

the limbs; and lastly, that the tips of the ears, nose, tail, and feet,

and the eye are emphasized in colour. In spotted animals the greatest

length of the spot is generally in the direction of the largest

development of the skeleton.

This morphological arrangement can be traced even when the decoration

has been modified. Thus, in the carnivora we have the lion and puma,

which live in open country, with plain skins, the tiger with stripes, an

inhabitant of the jungle, and the leopard, ocelot, and jaguar with

spots, inhabiting the forests.

But the lion has a dark dorsal stripe, and the nose, etc., are

emphasized in colour, and, moreover, the lion has probably lost its

marked decoration for protective purposes, for young lions are spotted.

The tiger's stripes start from the vertebræ, and still follow the lines

of the ribs. In the tiger the decoration changes at the neck, and on the

head, and the cervical vertebræ are often indicated by seven stripes.

See Fig. 5.

The markings over the vertebræ are not in continuous lines, as in many

mammals, but form a series of vertebra-like spots. This plan of

decoration is continued even on the tail, which is coloured more on the

upper than on the lower surface.

The spotted cats have their spot-groups arranged on the flanks in the

direction of the ribs, at the shoulder and haunch in curves, at the neck

in another pattern, on the back of the head in another; and the pattern

changes as each limb-joint is reached, the spots decreasing in size as

the distance is greater from the spine. See Figs. 9-15.

There is in tigers, and the cat-tribe generally, a dark stripe over the

dental nerve; and the zygoma, or cheek-bone, is often marked by colour.

Even the supraorbital nerve is shown in the forehead, and there are dark

rings round the ears. In dissecting an ocelot at the Zoological Gardens

in 1883, a forked line was found immediately over the fork of the

jugular vein.

The colouration in these animals seems often to be determined by the

great nerves and nerve-centres, and the change from spots, or stripes,

to wrinkled lines on the head are strikingly suggestive of the

convolutions of the brain, falling, as they do, into two lateral masses,

corresponding with the cerebral hemispheres, separated by a straight

line, corresponding with the median fissure. This is well shown in the

ocelot, Fig. 15, and in many other cats.

That the nerves can affect the skin has already been pointed out in

Chapter VI., in the case of herpes, and that it can affect colour is

shown in the Hindoo described in the same place.

So marked, indeed, is this emphasis of sensitive parts that every hair

of the movable feelers of a cat is shown by colour to be different in

function from the hairs of the neck, or from the stationary mass of hair

from which the single longer hair starts.

In the Badger, Fig. 16, there is a bulge-shaped mass of coloured hair

near the dorsal and lumbar regions, but it is axially placed. The

shoulder and loins are well marked, although in a different manner from

other species. In some species of deer, and other mammalia, there are

white or coloured lines parallel to the spine, and also, as in birds,

spots coalesce and form lines, and lines break up into spots.

The great anteater has what at first seems an exceptional marking on the

shoulder, but a careful examination of the fine specimen which died at

the Zoological Gardens in 1883, we were struck with the abnormal

character of the scapula, and we must remember that, as Wallace and

Darwin have pointed out, all abnormal changes of the teeth are

correlated with changes in the hair. Moreover the muscles of the

shoulder region are so enormously developed as to render this otherwise

defenceless animal so formidable that even the jaguar avoids an embrace

which tightens to a death-grip. This region is, therefore, precisely the

one we should expect to be strongly emphasized. This being the case, we

have really no exception in this creature.

Certain mammals are banded horizontally along their sides, thus losing

most of their axial decoration, and this is well shown among the

Viverridæ, and smaller rodents. Now, however conspicuous such animals

may appear in collections, they are in their native haunts very

difficult to detect. In all cases there is a marked dorsal line; and we

suggest that the mature decoration is due to a suppression of the axial

decoration for protective purposes, and a repetition of the dorsal

decoration according to the law before enunciated. Indeed, in one case

we were able to trace this pretty clearly, in the beautiful series of

_Sus vittatus_ in the museum at Leyden. This pig, an inhabitant of Java,

when mature is a dark brown animal, but in the very young state it is

clearly marked in yellow and brown, with a dark dorsal stripe, and

spots, taking the line of the ribs, and over the shoulder and thigh. As

the animal grows older, the spots run into stripes, and it becomes as

clearly banded horizontally as the viverridæ. Finally the dark bands

increase in width, until they unite, and the creature becomes almost

uniformly brown.

We have not been able to see young specimens of the viverridæ, but a

similar change may there occur, or it may have occurred in former times.

We must also remember that these creatures are long-bodied, like the

weasels, and hence they may have a tendency to produce long stripes.

In the case of our domestic animals, especially the oxen, the decoration

seems often to have become irregular, but even here the emphasis of the

extremities is generally clearly made out, and that of the limbs can

often be traced. In horses this is better shown, and dappled varieties

often well illustrate the points. Most horses at some time show traces

of spots.

Sufficient has now been said to point out the laws we believe to have

regulated the decoration of the animal kingdom. The full working out of

the question must be left to the future, but it is hoped that a solid

groundwork has been laid down.

[Illustration: Plate XI.

LEAVES.]

CHAPTER XV.

THE COLOURATION OF PLANTS.

The general structure of plants is so simple in comparison with that of

animals that our remarks upon this sub-kingdom need only be short.

With regard to leaves, especially such as are brightly coloured, like

the Begonias, Caladiums, Coleus, and Anoechtochilus, Plate XI., the

colour follows pretty closely the lines of structure. We have border

decoration, marking out the vein-pattern of the border; the veins are

frequently the seat of vivid colour, and when decolouration takes place,

as in variegated plants, we find it running along the interspaces of the

veins. These facts are too patent to need much illustration; for our

zonale geraniums, ribbon grasses, and beautiful-leaved plants generally,

are now so common that everyone knows their character. When decay sets

in, and oxidation gives rise to the vivid hues of autumn, we find the

tints taking structural lines, as is well shown in dying vine and

horse-chestnut leaves, Fig. 1, Plate XI. This shows us that there is a

structural possibility of acquiring regional colouration.

We must remember, too, that the negative colouration of these dying

leaves is of very much the same character as the positive colouration of

flowers, for flowers are modified leaves, and their hues are due to the

oxidation of the valuable chlorophyll.

In leaves the tendency of spots to elongate in the direction of the leaf

is very marked, as may be well seen in Begonia. Fig. 17, drawn to

illustrate another point, shows this partly. When leaves are

unsymmetrical, like the begonias, the pattern is unsymmetrical also.

Among parallel veined leaves we find parallel decoration. Thus, in the

_Calatheas_ we have dark marks running along the veins. In _Dracæna

ferrea_ we have a dark green leaf, with a red border and tip, the red

running downwards along the veins. This action may be continued until

the leaf is all red except the mid-rib, which remains green. In long

net-veined leaves we may cite _Pavetta Borbonica_, whose dark green

blade has a crimson mid-rib. Of unsymmetrical leaves those in the plate

may suffice.

When we come to flowers, the same general law prevails, and is generally

more marked in wild than in cultivated forms, which have been much, and

to some extent unnaturally, modified. Broadly speaking, when a flower is

regular the decoration is alike on all the parts; the petals are alike

in size, the decoration is similar in each, but where they differ in

size the decoration changes. Thus, in _Pelargoniums_ we may find all

five petals alike, or the two upper petals may be longer or shorter than

the lower three. In the first case each is coloured similarly, in the

other the colour pattern varies with the size of the petal. The same may

be seen in Rhododendron.

Where the petals are united the same law holds good. In regular flowers,

like the lilies, the colouration is equal. In irregular flowers, like

the snapdragon and foxglove, the decoration is irregular. In Gloxinia

the petals may be either regular or irregular, and the decoration

changes in concert.

A very instructive case was noticed by one of us in _Lamium

galeobdolon_, or yellow Archangel. This plant is normally a labiate with

the usual irregular corolla, but we have found it regular, and in this

instance the normal irregular decoration was changed to a regular

pattern on each petal.

In gamopetalous flowers the line of junction of the petals is frequently

marked with colour, and we know of no case in which a pattern runs

deliberately across this structure line, though a blotch may spread from

it.

When we remember that flowers are absolutely the result of the efforts

of plants to secure the fertilizing attention of insects, and that they

are supreme efforts, put forth at the expense of a great deal of

vegetable energy--that they are sacrifices to the necessity for

offspring--it does strike us forcibly when we see that even under these

circumstances the great law of structural decoration has to be adhered

to.

[Illustration: Plate XII.

FLOWERS.]

CHAPTER XVI.

CONCLUSIONS.

We have now, more or less fully, examined into the system of colouration

in the living world, and have drawn certain inferences from the facts

observed.

It appears that colouration began--perhaps as a product of digestion--by

the application of pigment to the organs of transparent creatures.

Supposing that evolution be true--and, if we may not accept this theory

there is no use in induction whatever--it must follow that even the

highest animals have in the past been transparent objects. This was

admirably illustrated by Prof. Ray Lankester in a lecture on the

development of the eyes of certain animals, before the British

Association meeting at Sheffield, in which it was shown that the eyes

commenced below the surface, and were useful even then, for its "body

was full of light."

Granting this, it follows that the fundamental law of decoration is a

structural one. Assuming, as we do, that memory has played a most

important part in evolution, it follows that all living matter has a

profound experience in decorating its organs--it is knowledge just as

anciently acquired, and as perfectly, as the power of digestion. This

colour was produced under the influence of light--so it is even in

opaque animals.

With a knowledge so far reaching, we might expect that even in opaque

animals the colouring would still follow structural lines, and there

should still be traces of this, more or less distinct.

This is precisely what we do find; and, moreover, we sometimes get a

very fair drawing of the important hidden parts, even where least

expected, as in a cat's head, a snake's body, a dragon-fly's thorax, a

spider's abdomen, a bird's skull.

But if animals thus learned to paint themselves in definite patterns, we

might expect that when called upon to decorate _for the sake of beauty_

certain parts not structurally emphatic, they would adopt well-known

patterns, and hence arose the law of repetition.

But with wider experience came greater powers, and the necessity for

protection arising, the well-known patterns were enlarged, till an

uniform tint is produced, as in the Java pig, or some repeated at the

expense of others, as in the civets. But so ingrained is the tendency to

structural decoration that even where modification has reached its

highest level, as in the leaf-butterflies, some trace of the plan that

the new pattern was founded on is recognisable, just as the rectangular

basis can be traced in the arabesque ornaments of the Alhambra.

The pointing out of this great fact has seemed to us a useful addition

to the great law of evolution. It supplements it; it gives a reason why.

Could he who first saw these points have read these final pages, it

would have lightened the responsibility of the one upon whom the

completion of the work has fallen. But he died when the work was nearly

finished. The investigation is of necessity incomplete, but nothing

bears such misstatements as truth, and though specialists may demur to

certain points, the fundamental arguments will probably remain intact.

[Illustration: FINIS.]

GLOSSARY.

ACETABULA. Lat. _acetabulum_, a little vessel. Sucking discs as on

the tentacles of _Physalia_.

AORTA. Gr. The chief artery.

CEPHALOTHORAX. Gr. _kephale_, head; _thorax_, chest. The anterior

division of the body in Crustacea and Arachnida, composed of the

amalgamated segments of the head and thorax.

CILIA. Lat. _cilium_, an eyelash. Microscopic filaments having the

power of vibratory movement.

C[OE]NOSARC. Gr. _Koinos_, common; _sarx_, flesh. The common stem

uniting the separate animals of compound hydrozoa, &c.

CORPUSCLE. Lat. _corpusculum_, a little body. Small coloured

bodies, as in the endoderm of hydra, p. 59.

DIFFERENTIATED. Modified into definite organs, or parts; as

distinct from structureless protoplasm.

ECTODERM. Gr. _ektos_, outside; _derma_, skin. The internal layer

or skin of the Coelenterata.

EFFERENT. Lat. _effero_, to carry out. A vessel which carries

fluids out of the body is said to be efferent.

ENDODERM. Gr. _endon_, within; _derma_, skin. The inner layer or

skin of Coelenterata. _See_ ECTODERM.

ENDOSARC. Gr. _endon_, within; _sarx_, flesh. The inner layer of

sponges.

EPIDERMAL. Gr. _epi_, upon; _derma_, skin. Relating to the outer

layer of skin. As applied to colour, surface pigment as distinct

from hypodermal, or deep-seated colour.

GASTROVASCULAR CANAL. Gr. _gaster_, belly; Lat. _vasculum_, a

little vessel. The canals or vessels in the umbrella (_manubrium_)

of hydrozoa.

GONIDIA. Gr. _gonos_, offspring; _oidos_, like. Reproductive bodies

in Sea-anemones.

HYDRANTH. Gr. _hudor_, water; _anthos_, flower. The bodies or

polypes of hydroids which exercise nutritive functions. They were

called polypites by Huxley.

HYDROPHYLLIA. Gr. _hudor_ and _phyllon_, a leaf. Leaf-like organs

protecting the polypites of hydrozoa.

HYDROSOMA. Gr. _hudor_ and _soma_, body. The entire organism of a

hydrozöon.

HYPODERMAL. Gr. _hypo_, beneath; _derma_, skin. In colour, such as

lies beneath the surface, as distinct from epidermal.

LYTHOCYSTS. Gr. _lythos_, stone, _kystis_, a bladder. Sense organs

in hydroids, consisting of transparent capsules inclosing round

transparent concretions.

MANUBRIUM. Lat. a handle. The central polypite suspended from the

interior of the umbrella of hydroids.

MESODERM. Gr. _mesos_, intermediate; _derma_, skin. The middle

layer of sponges, &c.

MESOTHORAX. Gr. _mesos_ and _thorax_. The middle division of the

thorax in insects, carrying the second pair of legs.

PERISTOME. Gr. _peri_, about; _stoma_, a mouth. The area

surrounding the mouth in sea-anemones.

PNEUMATOCYST. Gr. _pneuma_, air; _kystis_ a bladder. The air-sac

contained in the pneumatophore, see below.

PNEUMATOPHORE. Gr. _pneuma_; _phero_, to carry. The float of

certain hydrozoa (_Physophoridæ_.)

POLYPITE. Gr. _polus_, many; _pous_, foot. The separate animal or

zöoid of a hydrozöon. _See_ HYDRANTH.

PROTOPLASM. Gr. _protos_, first; _plasso_, I mould. The jelly-like

matter which forms the basis of all tissues. It is identical with

the _sarcode_ or flesh of protozoa.

SAC. Lat. _saccus_, a bag, a small cell.

SARCODE. Gr. _sarx_, flesh; _eidos_, form. The protoplasm of

protozoa, &c., which see.

SPADIX. Lat. _spadix_, a broken palm branch. In zoology a hollow

process occupying the axis of the generative buds of hydrozoa.

SPOROSAC. Gr. _spora_, a seed, and _sac_. The body containing the

ova of hydrozoa.

SOMATIC FLUID. Gr. _soma_, the body. The fluid which contains

digested food, and taking the place of blood, circulates through

the body of hydrozoa.

TENTACLES. Lat. _tentaculus_, a little arm. The arms or prehensile

organs of Sea-anemones, &c.

THREAD CELLS. Cells containing an extensible microscopic thread,

possessing stinging properties, common among the _Coelenterata_.

THORAX. Gr. a breastplate. The chest.

INDEX.

PAGE

_Abyla_ 63

_Acanthometra_ 57

_Actinea Cari_, varieties of 66

---- _mesembryanthemum_ 54

_Acanthostratus_ 57

_Actinozoa_ 51, 52

_Æschna_ 77

_Agalma breve_ 64

_Agrion puella_ 77

_Aiptasia mutabilis_ 67

Albinism in butterflies 79

_Alcyonariæ_ 54

Allman, Prof., on Hydroids 59, 60

"Alps and Sanctuaries" quoted 36

_Amoeba_ 56

Amphibia 89

_Amphilonche_ 57

Andres, Dr., on Hydrozoa 65

_Anemonia sulcata_ 67

Anemones, Sea 52

Animals and Plants, origin of 36

---- classification of 49

_Anoechtochilus_ 95

Anteater 93

_Anthocaris belemia_ 41

---- _belia_ 42

---- _cardamines_ 41, 42

---- _euphemoides_ 43

---- _eupheno_ 42

---- _simplonia_ 42

_Apatura iris_ 46

---- larvæ of 81

_Arachnida_ 82

_Araschnia Levana_ 43, 45

---- _porima_ 43, 45, 79

---- _prorsa_ 43, 45

_Arctia_ 69

_Arachnocorys_ 57

Argus Pheasant 6, 39, 91

_Argynnis Lathonia_ 69

Armadillo 84

Arthropoda, colouration of 85

Ascidians 35

Automatic habits 9

_Arthorybia rosacea_ 64

Badger 93

_Begonia_ 95

Birds, colouration of 89

---- of Paradise 90

_Biston betularia_ 79

Black and White, production of 28

Blackwell, J., on British Spiders 82

_Blatta_ 14

Bougainvillea 16

Bower Birds 5

_Bunodes crassicornis_ 54

---- _gemmaceus_, varieties of 66

---- _rigidus_ 67

Burnet Moths 5, 69

Butler S., on inherited memory 9, 10, 11, 15

---- on origin of animals and plants 36

Butterflies, albinism in 79

---- classification of 74

---- sense organs of 30

---- varieties of 77

_Caladium_ 95

_Calathea_ 96

_Calycophoridæ_ 63

_Carcinus moenas_ 4

_Carpocanium_ 57

Cats, colouration of 17, 92

---- recognising form 32

Caterpillars, colours of 81

---- spiracular markings 22

_Cephalopoda_ 87

_Cerithium_ 86

Char 88

Chlorophyll in hydra 59

Cicada 77

_Cladococeus_ 57

Classification of animals 49

---- of butterflies 74

_Coelenterata_ 20

---- colouration in 51

_Coelodendrum_ 57

_Coenonympha davus_ 79

---- _pamphilus_ 79

Coenosarc 55

_Coleus_ 95

Colour and form 32

---- and transparency 53

---- epidermal 72

---- following structure 83, 91

---- hypodermal 53, 73

---- nature of 25

---- of day-and-night flying insects 47, 69

---- opaque 53

---- perception of 5, 23, 25, 32

---- uniform, why rare 28

Colouration 3

---- laws of 21, 51

---- of desert animals 4

---- of arthropoda 85

---- of coelenterata 51, 59

---- of insects 68

---- of invertebrata 49

---- of molluscs 85

---- of plants 94

---- of protozoa 51

---- of spiders 82

---- of vertebrata 88

---- sexual 5

---- varieties of 3

Contour feathers 91

_Conus_ 86

_Coppinia arcta_ 60

_Corallium rubrum_ 54

Corals 54

Correlation of teeth and hair 94

_Corynida_ 52

Cowries 86

Crab, shore 4

Croton 46

Cuttle-fishes 19, 87

_Cyllo leda_ 45

_Cynthia cardui_ 68

_Cypræa_ 86

_Cyrtidosphæra_ 57

Dallas, W. S., on butterflies 71

_Danais_ 72

---- niavius 30, 80

Darwin, C. 1, 2, 5, 9, 11, 14, 45, 47, 94

Darwin, Dr. E., cited 37

Deer 92

Deformity, antipathy to 32

_Deilephila Euphorbiæ_ 81

---- _galii_ 81

Descent with modification 1

Desert animals, colour of 4

_Dictyoceras_ 57

_Dictyophimus_ 57

_Diphyes_ 63

Disease, markings in 39, 44

Distant, W. L., on Malayan butterflies 80

Distinctive Colouration 3

Dogs recognising portraits 32

_Dracæna ferrea_ 96

Elephant, increase of 2

Engelmann on _Euglena_ 34

Epidermal colour 72

_Eresus cinnabarinus_ 82

_Eucecryphalus_ 57

_Eucrytidium_ 57

_Euglena viridis_ 34

Evolution 1-98

Eye-spots 45, 47

Fayrer, Sir W., on snakes 89

Feathers 91

Fishes, colours of 88

Foal, stripes on 46

_Foraminiferæ_ 56

Fuller, W. J., on aquatic larvæ 77

Gamopetalous flowers 96

Gegenbaur's "Comparative Anatomy" cited 82

General colouration 3

_Gloxinia_ 96

_Gomphina_ 77

_Gonepteryx Cleopatra_ 41, 42

---- _rhamni_ 40, 42

Gonophores 52

_Grapta interrogationis_ 79

_Gregarinidæ_ 56

Guinea-fowl 91

Haagen, Dr., on colour 53, 72

Habits 8

Haeckel, Prof., on _Radiolaria_ 57

Hair and teeth, correlation of 94

Hawk moths 69

Hebrides, colours of insects in 80

Heredity 2

Herpes 40, 93

Heteromorphism 78

Higgins, Rev. H. H. 39

Hoverer flies 84

Humming birds 90, 92

Hutchinson, Mr., on herpes 40

Huxley, Prof., on hydrozoa 63

_Hydra viridis_ 59

_Hydrida_ 59

Hydrozoa 51, 59

Hypodermal colour 53, 72

Identity of offspring and parent 11

Identity, personal 10

Inherited memory 8

Insects, colour in 68, 75

John Dory 89

_Kallima inachus_ 30, 80

Kentish Glory Moth 30

_Lamium galeobdolon_ 96

Lankester, Prof. Ray, on development of eyes 97

Large Copper Butterfly 68

Larvæ, colours of 45, 81

Laws of emphasis 21

---- exposure 18

---- heredity 2

---- multiplication 2

---- repetition 21, 22

---- structure 18

---- variation 2

Leaf-butterfly 16, 30

Leidy, Prof., on _Rhizopoda_ 56

Leopard 17, 92

_Leucophasia diniensis_ 41

---- _sinapis_ 41

"Life and Habit" cited 9

Light, reflected 26

---- sensibility to 33

---- waves 25

_Liminitis sibilla_ 43

Lion 17, 92

---- stripes on young 46

Lithocysts of hydroids 62

_Lucernaria auricula_ 65

_Lycæna dispar_ 68

_Lycosa agretyca_ 83

---- _allodroma_ 83

---- _andrenivora_ 83

---- _cambria_ 84

---- _campestris_ 83

---- _latitans_ 84

---- _picta_ 84

---- _piratica_ 84

---- _rapax_ 83

Mackerel 88

_Mactra_ 86

---- _stultorum_ 87

Madrepores 54

Mammalia, colouration in 92

_Margarita catenata_ 87

Measles 39

Medusæ 52, 65

Melanism in insects 79

Meldola, Prof. R., on Melanism 79

_Melitæa artemis_ 43

---- _athalia_ 43

Mimicry 3, 4

Mollusca 21

---- colouration in 85

Monstrosities, antipathy to 32

_Morphinæ_ 72

_Morpho_ 4

_Murex_ 86

Muscles of insects 71

_Nectarinea chloropygea_ 90

Newman, Mr., on varieties of butterflies 77

Newts 89

Nitzsch on feather-tracts 91

Nudibranchs 85

_Nymphalidæ_ 74

Oak Egger Moth 30

Ocelli 47

Ocelot 93

_Oliva_ 86

Opaque colouring 53

Organ-pipe coral 54

Origin of animals and plants 36

---- -- species 1

Orthopoecilism 78

Oxen 94

Painted Lady Butterfly 68

Pangenesis 12

_Papilio Ajax_ 79

---- _machaon_ 43, 68, 76, 78

---- ---- larva of 81

---- _merope_ 30, 76, 80

---- _nireus_ 14

---- _podalirius_ 43

_Paradisea Papuana_ 90

---- _regia_ 90

---- _speciosa_ 90

---- _Wallacei_ 90

---- _Wilsoni_ 90, 91

_Pavetta Borbonica_ 96

_Pecten_ 86

Pelargonium 96

Perch 88

Personal identity 10

_Physalia_ 63

---- _caravilla_ 64

---- _pelagica_ 64

---- _utriculus_ 64

_Physophoridæ_ 63

Plaice 88

Plants and animals, origin of 36

---- colour in 95

Pneumatophores 63

Portuguese Man o' War 63

Protective resemblance 3

_Protista_ 34

Protozoa 20

---- colouration in 51, 56

Python 89

_Radiolaria_ 57

Rarity of uniform colour 28

Ray Lankester, Prof., on Ascidians 35

Red Admiral Butterfly 29

Repetition, effects of 8

Reptilia, colouration in 89

Resemblance, Protective 3

_Rhizophora filiformis_ 64

_Rhizopoda_ 56

Rhododendron 96

Ringlet Butterflies, eye-spots of 47

Roach 88

Romanes, Prof., cited 33, 34

_Satyrus hyperanthus_ 79

Scales of insects, structure of 72

Scarlet Tiger Moth 5

Sea anemones 52

---- ---- colours of 67

Seasonal dimorphism 70

Sea squirts 35

_Segestria senoculata_ 83

Selection, sexual 5

Self-coloured flowers 28

Sense organs of Butterflies 30

_Sertularidæ_ 63

Sexual colours 4

---- selection 5

---- dimorphism 70

Shell, Structure of 85

Shore Crab 4

Simple variation in Butterflies 77

_Siphonophora_ 63

Small pox 39

Snakes, patterns of 89

Sollas, Prof., on Sponges 58

Soles 88

_Sparassus smaragdulus_ 82

Species, origin of 1

_Sphæronectes_ 63

_Sphingidæ_ 45, 69

Spiders, structure and colour of 82

Spiracles of larvæ 22

_Spondylus_ 86

Sponges 57

_Spongida_ 57

_Spongocyclia_ 57

Spots and Stripes 39

_Stephanomia amphitridis_ 63

Struggle for existence 2

Sun-birds 90

_Sus vittatus_ 46, 94

Sutton, Mr. Bland, on Herpes 40

Swallow-tailed Butterflies 68

_Syncoryne pulchella_ 62

Systems of colouration 51

Teeth and Hair, correlation of 94

_Thomisus cinereus_ 82

---- _floricolens_ 82

_Thomisus luctuosus_ 84

---- _trux_ 82

Thrush, increase of 2

Tiger 17, 92

---- Moths 69

_Tipula_ 33

Toucans 90, 92

Transparency and colour 53

_Trigonia_ 86

_Tubipora musica_ 54

_Tubularida_ 59

Tylor, A., on Specific change 10

_Vanessa Antiopa_ 76

---- _atalanta_ 29, 43, 69

---- _urticæ_ 77

Variation in insects 70

---- law of 2

---- simple, in Butterflies 77

_Velella_ 52, 65

Vertebrata, colouration of 88

_Viverridæ_ 94

Wallace, A. R., on sexual selection 5, 6, 14, 15

---- on colour 29

---- on abnormal structures 94

Warning colours 4

Wasps 84

Weir, J. Jenner, on variation in insects 78

Weismann, Dr., on Caterpillars 81

Wing of Butterfly, typical 70

---- patterns of 76

Woodpecker 91

Yellow Archangel 96

Zebra 92

_Zygæna_ 69

[Illustration]

[Illustration: Fig. 4.--PYTHON.

_Showing vertebra-like markings._]

[Illustration: Fig. 5.--TIGER.

_The pattern changes at the points lettered._]

[Illustration: Fig. 6.--TIGER.]

[Illustration: Fig. 7.--TIGER.

_Showing supra-orbital nerve mark._]

[Illustration: Fig. 8.--TIGER.

_Showing cerebral markings, and markings over

nerves near the eyes._]

[Illustration: Fig. 9.--LEOPARD.

_The pattern changes at the points lettered._]

[Illustration: Fig. 10.--LEOPARD.

_The pattern changes at the points lettered._]

[Illustration: Figs. 11, 12.--LEOPARDS' HEADS.]

[Illustration: Fig. 13.--LYNX.

_The colour changes at the points lettered._]

[Illustration: Fig. 14.--LYNX.]

[Illustration: Fig. 15.--OCELOT.

_Showing changes of pattern at the joints, &c.,

with enlargement of head-pattern._]

[Illustration: Fig. 16.--BADGER.

_The colour changes at the points lettered._]

[Illustration: Fig. 17.--BEGONIA LEAF.]

Transcriber's Notes:

Variations in spelling, punctuation and hyphenation have been retained

except in obvious cases of typographical error.

"Haeckel" and "Hæckel" were used interchangeably and have been

standardized to "Haeckel".

Image tags interrupting paragraphs have been moved.

Footnotes have been moved to end of chapters.

End of Project Gutenberg's Colouration in Animals and Plants, by Alfred Tylor

Colouration in Animals and Plants · 第 11 / 11 章