On the Genesis of Species Part 2

"The approach in colour and form to the Heliconidae, however, would be at the first a positive, though perhaps a slight, advantage; for although at short distances this variety would be easily distinguished and devoured, yet at a longer distance it might be mistaken for one of the uneatable group, and so be pa.s.sed by and gain another day's life, which might in many cases be sufficient for it to lay a quant.i.ty of eggs and leave a numerous progeny, many of which would inherit the peculiarity which had been the safeguard of their parent."

[Ill.u.s.tration: LEAF b.u.t.tERFLY IN FLIGHT AND REPOSE.

(_From Mr. Wallace's_ "_Malay Archipelago._")]

As a complete example of mimicry Mr. Wallace refers to a common Indian b.u.t.terfly. He says:[26] "But the most wonderful and undoubted case of protective resemblance in a b.u.t.terfly, which I have ever seen, is that {31} of the common Indian _Kallima inachis_, and its Malayan ally, _Kallima paralekta_. The upper surface of these is very striking and showy, as they are of a large size, and are adorned with a broad band of rich orange {32} on a deep bluish ground. The under side is very variable in colour, so that out of fifty specimens no two can be found exactly alike, but every one of them will be of some shade of ash, or brown, or ochre, such as are found among dead, dry, or decaying leaves. The apex of the upper wings is produced into an acute point, a very common form in the leaves of tropical shrubs and trees, and the lower wings are also produced into a short narrow tail. Between these two points runs a dark curved line exactly representing the midrib of a leaf, and from this radiate on each side a few oblique lines, which serve to indicate the lateral veins of a leaf. These marks are more clearly seen on the outer portion of the base of the wings, and on the inner side towards the middle and apex, and it is very curious to observe how the usual marginal and transverse striae of the group are here modified and strengthened so as to become adapted for an imitation of the venation of a leaf." ... "But this resemblance, close as it is, would be of little use if the habits of the insect did not accord with it. If the b.u.t.terfly sat upon leaves or upon flowers, or opened its wings so as to expose the upper surface, or exposed and moved its head and antennae as many other b.u.t.terflies do, its disguise would be of little avail. We might be sure, however, from the a.n.a.logy of many other cases, that the habits of the insect are such as still further to aid its deceptive garb; but we are not obliged to make any such supposition, since I myself had the good fortune to observe scores of _Kallima paralekta_, in Sumatra, and to capture many of them, and can vouch for the accuracy of the following details. These b.u.t.terflies frequent dry forests, and fly very swiftly. They were seen to settle on a flower or a green leaf, but were many times lost sight of in a bush or tree of dead leaves. On such occasions they were generally searched for in vain, for while gazing intently at the very spot where one had disappeared, it would often suddenly dart out, and again vanish twenty or fifty yards further on. On one or two occasions the insect was detected{33} reposing, and it could then be seen how completely it a.s.similates itself to the surrounding leaves. It sits on a nearly upright twig, the wings fitting closely back to back, concealing the antennae and head, which are drawn up between their bases. The little tails of the hind wing touch the branch, and form a perfect stalk to the leaf, which is supported in its place by the claws of the middle pair of feet, which are slender and inconspicuous.

The irregular outline of the wings gives exactly the perspective effect of a shrivelled leaf. We thus have size, colour, form, markings, and habits, all combining together to produce a disguise which may be said to be absolutely perfect; and the protection which it affords is sufficiently indicated by the abundance of the individuals that possess it."

Beetles also imitate bees and wasps, as do some Lepidoptera; and objects the most bizarre and unexpected are simulated, such as dung and drops of dew. Some insects, called bamboo and walking-stick insects, have a most remarkable resemblance to pieces of bamboo, to twigs and branches. Of these latter insects Mr. Wallace says:[27] "Some of these are a foot long and as thick as one's finger, and their whole colouring, form, rugosity, and the arrangement of the head, legs, and antennae, are such as to render them absolutely identical in appearance with dry sticks. They hang loosely about shrubs in the forest, and have the extraordinary habit of stretching out their legs unsymmetrically, so as to render the deception more complete."

Now let us suppose that the ancestors of these various animals were all dest.i.tute of the very special protections they at present possess, as on the Darwinian hypothesis we must do. Let it also be conceded that small deviations from the antecedent colouring or form would tend to make some of their ancestors escape destruction by causing them more or less frequently to be pa.s.sed over, or mistaken by their persecutors. Yet the deviation {34} must, as the event has shown, in each case be in some definite direction, whether it be towards some other animal or plant, or towards some dead or inorganic matter. But as, according to Mr. Darwin's theory, there is a constant tendency to indefinite variation, and as the minute incipient variations will be in _all directions_, they must tend to neutralize each other, and at first to form such unstable modifications that it is difficult, if not impossible, to see how such indefinite oscillations of infinitesimal beginnings can ever build up a sufficiently appreciable resemblance to a leaf, bamboo, or other object, for "Natural Selection" to seize upon and perpetuate. This difficulty is augmented when we consider--a point to be dwelt upon hereafter--how necessary it is that many individuals should be similarly modified simultaneously. This has been insisted on in an able article in the _North British Review_ for June 1867, p. 286, and the consideration of the article has occasioned Mr. Darwin to make an important modification in his views.[28]

In these cases of mimicry it seems difficult indeed to imagine a reason why variations tending in an _infinitesimal degree_ in any special direction should be preserved. All variations would be preserved which tended to obscure the perception of an animal by its enemies, whatever direction those variations might take, and the common preservation of conflicting tendencies would greatly favour their mutual neutralization and obliteration if we may rely on the many cases recently brought forward by Mr. Darwin with regard to domestic animals.

[Ill.u.s.tration: THE WALKING-LEAF INSECT.]

Mr. Darwin explains the imitation of some species by others more or less nearly allied to it, by the common origin of both the mimic and the mimicked species, and the consequent possession by both (according to the theory of "Pangenesis") of gemmules tending to reproduce ancestral characters, which characters the mimic must be a.s.sumed first to have {35} lost and then to have recovered. Mr. Darwin says,[29] "Varieties of one species frequently mimic distinct species, a fact in perfect harmony with the foregoing cases, and explicable _only on the theory of descent_." But this at the best is but a partial and very incomplete explanation. It is one, moreover, which Mr. Wallace does not accept.[30] It is very incomplete, because it has no bearing on some of the most striking cases, and of course Mr. Darwin does not pretend that it has. We should have to go back far indeed to reach the common ancestor of the mimicking {36} walking-leaf insect and the real leaf it mimics, or the original progenitor of both the bamboo insect and the bamboo itself. As these last most remarkable cases have certainly nothing to do with heredity,[31] it is unwarrantable to make use of that explanation for other protective resemblances, seeing that its inapplicability, in certain instances, is so manifest.

Again, at the other end of the process it is as difficult to account for the last touches of perfection in the mimicry. Some insects which imitate leaves extend the imitation even to the very injuries on those leaves made by the attacks of insects or of fungi. Thus, speaking of one of the walking-stick insects, Mr. Wallace says:[32] "One of these creatures obtained by myself in Borneo (_Ceroxylus laceratus_) was covered over with foliaceous excrescences of a clear olive-green colour, so as exactly to resemble a stick grown over by a creeping moss or jungermannia. The Dyak who brought it me a.s.sured me it was grown over with moss although alive, and it was only after a most minute examination that I could convince myself it was not so." Again, as to the leaf b.u.t.terfly, he says:[33] "We come to a still more extraordinary part of the imitation, for we find representations of leaves in every stage of decay, variously blotched, and mildewed, and pierced with holes, and in many cases irregularly covered with powdery black dots, gathered into patches and spots, so closely resembling the various kinds of minute fungi that grow on dead leaves, that it is impossible to avoid thinking at first sight that the b.u.t.terflies themselves have been attacked by real fungi."

Here imitation has attained a development which seems utterly beyond the power of the mere "survival of the fittest" to produce. How this double mimicry can importantly aid in the struggle for life seems puzzling indeed, but much more so how the first faint beginnings of the imitation of {37} such injuries in the leaf can be developed in the animal into such a complete representation of them--_a fortiori_ how simultaneous and similar first beginnings of imitations of such injuries could ever have been developed in several individuals, out of utterly indifferent and indeterminate infinitesimal variations in all conceivable directions.

[Ill.u.s.tration: PLEURONECTIDae, WITH THE PECULIARLY PLACED EYE IN DIFFERENT POSITIONS.

(_From Dr. Traquair's paper in the "Transactions of the Linnean Society, 1865."_)]

Another instance which may be cited is the asymmetrical condition of the heads of the flat-fishes (Pleuronectidae), such as the sole, the flounder, the brill, the turbot, &c. In all these fishes the two eyes, which in the young are situated as usual one on each side, come to be placed, in the adult, both on the same side of the head. If this condition had appeared at once, if in the hypothetically fortunate common ancestor of these fishes an eye had suddenly become thus transferred, then the perpetuation of such a transformation by the action of "Natural Selection" is conceivable enough.

Such sudden changes, however, are not those favoured by the Darwinian theory, and indeed the accidental occurrence of such a spontaneous transformation is hardly conceivable. But if this is not so, if the transit was gradual, then how such transit of one eye a minute fraction of the {38} journey towards the other side of the head could benefit the individual is indeed far from clear. It seems, even, that such an incipient transformation must rather have been injurious. Another point with regard to these flat-fishes is that they appear to be in all probability of recent origin--_i.e._ geologically speaking. There is, of course, no great stress to be laid on the mere absence of their remains from the secondary strata, nevertheless that absence is noteworthy, seeing that existing fish families, _e.g._ sharks (Squalidae), have been found abundantly even down so far as the carboniferous rocks, and traces of them in the Upper Silurian.

Another difficulty seems to be the first formation of the limbs of the higher animals. The lowest Vertebrata[34] are perfectly limbless, and if, as most Darwinians would probably a.s.sume, the primeval vertebrate creature was also apodal, how are the preservation and development of the first rudiments of limbs to be accounted for--such rudiments being, on the hypothesis in question, infinitesimal and functionless?

In reply to this it has been suggested that a mere flattening of the end of the body has been useful, such, _e.g._, as we see in sea-snakes,[35] which may be the rudiment of a tail formed strictly to aid in swimming. Also that a mere _roughness_ of the skin might be useful to a swimming animal by holding the water better, that thus minute processes might be selected and preserved, and that, in the same way, these might be gradually increased into limbs. But it is, to say the least, very questionable whether a roughness of the skin, or minute processes, would be useful to a {39} swimming animal; the motion of which they would as much impede as aid, unless they were at once capable of a suitable and appropriate action, which is against the hypothesis. Again, the change from mere indefinite and accidental processes to two regular pairs of symmetrical limbs, as the result of merely fortuitous, favouring variations, is a step the feasibility of which hardly commends itself to the reason, seeing the very different positions a.s.sumed by the ventral fins in different fishes. If the above suggestion made in opposition to the views here a.s.serted be true, then the general constancy of position of the limbs of vertebrata may be considered as due to the position a.s.sumed by the primitive rugosities from which those limbs were generated. Clearly only two pairs of rugosities were so preserved and developed, and all limbs (on this view) are descendants of the same two pairs, as all have so similar a fundamental structure. Yet we find in many fishes the pair of fins, which correspond to the hinder limbs of other animals, placed so far forwards as to be either on the same level with, or actually in front of, the normally anterior pair of limbs; and such fishes are from this circ.u.mstance called "thoracic," or "jugular"

fishes respectively, as the weaver fishes and the cod. This is a wonderful contrast to the fixity of position of vertebrate limbs generally. If then such a change can have taken place in the comparatively short time occupied by the evolution of these special fish forms, we might certainly expect other and far more bizarre structures would (did not some law forbid) have been developed, from other rugosities, in the manifold exigencies of the mult.i.tudinous organisms which must (on the Darwinian hypothesis) have been gradually evolved during the enormous period intervening between the first appearance of vertebrate life and the present day. Yet, with these exceptions, the position of the limbs is constant from the lower fishes up to man, there being always an anterior pectoral pair placed in front of a posterior or pelvic pair when both are present, and in no single {40} instance are there more than these two pairs.

[Ill.u.s.tration: MOUTH OF A WHALE.]

The development of whalebone (baleen) in the mouth of the whale is another difficulty. A whale's mouth is furnished with very numerous h.o.r.n.y plates, which hang down from the palate along each side of the mouth. They thus form two longitudinal series, each plate of which is placed transversely to the long axis of the body, and all are very close together. On depressing the lower lip the free outer edges of these plates come into view. Their inner edges are furnished with numerous coa.r.s.e hair-like processes, consisting of some of the const.i.tuent fibres of the h.o.r.n.y plates--which, as it were, fray out--and the mouth is thus lined, except below, by a network of countless fibres formed by the inner edges of the two series of plates.

This network acts as a sort of sieve. When the whale feeds it takes {41} into its mouth a great gulp of water, which it drives out again through the intervals of the h.o.r.n.y plates of baleen, the fluid thus traversing the sieve of h.o.r.n.y fibres, which retains the minute creatures on which these marine monsters subsist. Now it is obvious, that if this baleen had once attained such a size and development as to be at all useful, then its preservation and augmentation within serviceable limits, would be promoted by "Natural Selection" alone. But how to obtain the beginning of such useful development? There are indeed certain animals of exclusively aquatic habits (the dugong and manatee) which also possess more or less horn on the palate, and at first sight this might be taken as a mitigation of the difficulty; but it is not so, and the fact does not help us one step further along the road: for, in the first place, these latter animals differ so importantly in structure from whales and porpoises that they form an altogether distinct order, and cannot be thought to approximate to the whale's progenitors. They are vegetarians, the whales feed on animals; the former never have the ribs articulated in the mode in which they are in some of the latter; the former have pectoral mammae, and the latter are {42} provided with two inguinal mammary glands, and have the nostrils enlarged into blowers, which the former have not. The former thus const.i.tute the order Sirenia, while the latter belong to the Cetacea. In the second place, the h.o.r.n.y matter on the palates of the dugong and manatee has not, even initially, that "strainer" action, which is the characteristic function of the Cetacean "baleen."

[Ill.u.s.tration: FOUR PLATES OF BALEEN SEEN OBLIQUELY FROM WITHIN.]

[Ill.u.s.tration: DUGONG.]

There is another very curious structure, the origin or the disappearance of which it seems impossible to account for on the hypothesis of minute indefinite variations. It is that of the mouth of the young kangaroo. In all mammals, as in ourselves, the air-pa.s.sage from the lungs opens in the floor of the mouth behind the tongue, and in front of the opening of the gullet, so that each particle of food as it is swallowed pa.s.ses over the opening, but is prevented from falling into it (and thus causing death from choking) by the action of a small cartilaginous s.h.i.+eld (the epiglottis), which at the right moment bends back and protects the orifice. Now the kangaroo is born in such an exceedingly imperfect and undeveloped condition, that it is quite unable to suck. The mother therefore places the minute blind and naked young upon the nipple, and then injects milk into it by means of a special muscular envelope of the mammary gland. Did no special provision exist, the young one must infallibly be choked by the intrusion of the milk into the windpipe. But there _is_ a special provision. The larynx is so elongated that it rises up into the posterior end of the nasal pa.s.sage, and is thus enabled to give free entrance to the air for the lungs, while the milk pa.s.ses harmlessly on each side of this elongated larynx, and so safely attains the gullet behind it.

Now, on the Darwinian hypothesis, either all mammals descended from marsupial progenitors, or else the marsupials, sprung from animals having in most respects the ordinary mammalian structure. [Page 43]

On the first alternative, how did "Natural Selection" remove this (at least perfectly innocent and harmless) structure in almost all other mammals, and, having done so, again reproduce it in precisely those forms which alone require it, namely, the Cetacea? That such a harmless structure _need not_ be removed any Darwinian must confess, since a structure exists in both the crocodiles and gavials, which enables the former to breathe themselves while drowning the prey which they hold in their mouths. On Mr.

Darwin's hypothesis it could only have been developed where useful, therefore not in the gavials(!) which feed on fish, but which yet retain, as we might expect, this, in them superfluous but harmless formation.

On the second alternative, how did the elongated larynx itself arise, seeing that if its development lagged behind that of the maternal structure, the young primeval kangaroo must be choked: while without the injecting power in the mother, it must be starved? The struggle by the sole action of which such a form was developed must indeed have been severe!

[Ill.u.s.tration: AN ECHINUS, OR SEA-URCHIN (The spines removed from one-half.)]

The sea-urchins (Echinus) present us also with structures the origin of which it seems impossible to explain by the action of "Natural {44} Selection" only. These lowly animals belong to that group of the star-fish cla.s.s (Echinodermata), the species of which possess generally spheroidal bodies, built up of mult.i.tudinous calcareous plates, and const.i.tute the order Echinoidea. They are also popularly known as sea-eggs. Utterly devoid of limbs, the locomotion of these creatures is effected by means of rows of small tubular suckers (which protrude through pores in the calcareous plates) and by moveable spines scattered over the body.

[Ill.u.s.tration: PEDICELLARIae. (Immensely enlarged.)]

Besides these spines and suckers there are certain very peculiar structures, termed "Pedicellariae." Each of these consists of a long slender stalk, ending in three short limbs--or rather jaws--the whole supported by a delicate internal skeleton. The three limbs (or jaws), which start from a common point at the end of the stalk, are in the constant habit of opening and closing together again with a snapping action, while the stalk itself sways about. The utility of these appendages is, even now, problematical.

It may be that they remove from the surface of the animal's body foreign substances which would be prejudicial to it, and which it cannot otherwise get rid of. But granting this, what would be the utility of the _first rudimentary beginnings_ of such structures, and how could such incipient buddings have ever preserved the life of a single Echinus? It is true that on Darwinian principles the ancestral form from which the sea-urchin developed was different, and must not be conceived merely as an Echinus devoid of pedicellariae; but this makes the difficulty none the less. It is equally hard to imagine that the first rudiments of such structures could have been useful to _any_ animal from which the Echinus might have been{45} derived. Moreover, not even the _sudden_ development of the snapping action could have been beneficial without the freely moveable stalk, nor could the latter have been efficient without the snapping jaws, yet no minute merely indefinite variations could simultaneously evolve these complex co-ordinations of structure; to deny this seems to do no less than to affirm a startling paradox.

Mr. Darwin explains the appearance of some structures, the utility of which is not apparent, by the existence of certain "laws of correlation." By these he means that certain parts or organs of the body are so related to other organs or parts, that when the first are modified by the action of "Natural Selection," or what not, the second are simultaneously affected, and increase proportionally or possibly so decrease. Examples of such are the hair and teeth in the naked Turkish dog, the general deafness of white cats with blue eyes, the relation between the presence of more or less down on young birds when first hatched, and the future colour of their plumage,[36] with many others. But the idea that the modification of any internal or external part of the body of an Echinus carries with it the effect of producing elongated, flexible, triradiate, snapping processes, is, to say the very least, fully as obscure and mysterious as what is here contended for, viz. the efficient presence of an unknown internal natural law or laws conditioning the evolution of new specific forms from preceding ones, modified by the action of surrounding conditions, by "Natural Selection" and by other controlling influences.

The same difficulty seems to present itself in other examples of exceptional structure and action. In the same Echinus, as in many allied forms, and also in some more or less remote ones, a very peculiar mode of development exists. The adult is not formed from the egg directly, but {46} the egg gives rise to a creature which swims freely about, feeds, and is even somewhat complexly organized. Soon a small lump appears on one side of its stomach; this enlarges, and, having established a communication with the exterior, envelopes and appropriates the creature's stomach, with which it swims away and develops into the complete adult form, while the dispossessed individual perishes.

Again, certain flies present a mode of development equally bizarre, though quite different. In these flies, the grub is, as usual, produced from the ovum, but this grub, instead of growing up into the adult in the ordinary way, undergoes a sort of liquefaction of a great part of its body, while certain patches of formative tissue, which are attached to the ramifying air tubes, or tracheae (and which patches bear the name of "imaginal disks"), give rise to the legs, wings, eyes, &c., respectively; and these severally formed parts grow together, and build up the head and body by their mutual approximation. Such a process is unknown outside the cla.s.s of insects, and inside that cla.s.s it is only known in a few of the two-winged flies. Now, how "Natural Selection," or any "laws of correlation," can account for the gradual development of such an exceptional process of development--so extremely divergent from that of other insects--seems nothing less than inconceivable. Mr. Darwin himself[37] gives an account of a very peculiar and abnormal mode of development of a certain beetle, the sitaris, as described by M. Fabre. This insect, instead of at first appearing in its grub stage, and then, after a time, putting on the adult form, is at first active and furnished with six legs, two long antennae, and four eyes. Hatched in the nests of bees, it at first attaches itself to one of the males, and then crawls, when the opportunity offers, upon a female bee. When the female bee lays her eggs, the young sitaris springs upon them and devours them. Then, losing its eyes, legs, and antennae, and {47} becoming rudimentary, it sinks into an ordinary grub-like form, and feeds on honey, ultimately undergoing another transformation, re-acquiring its legs, &c., and emerging a perfect beetle! That such a process should have arisen by the acc.u.mulation of minute accidental variations in structure and habit, appears to many minds, quite competent to form an opinion on the subject, absolutely incredible.

It may be objected, perhaps, that these difficulties are _difficulties of ignorance_--that we cannot explain them because we do not know _enough_ of the animals. But it is here contended that this is not the case; it is not that we merely fail to see how Natural Selection acted, but that there is a positive incompatibility between the cause a.s.signed and the results. It will be stated shortly what wonderful instances of co-ordination and of unexpected utility Mr. Darwin has discovered in orchids. The discoveries are not disputed or undervalued, but the explanation of their _origin_ is deemed thoroughly unsatisfactory--utterly insufficient to explain the incipient, infinitesimal beginnings of structures which are of utility only when they are considerably developed.

Let us consider the mammary gland, or breast. Is it conceivable that the young of any animal was ever saved from destruction by accidentally sucking a drop of scarcely nutritious fluid from an accidentally hypertrophied cutaneous gland of its mother? And even if one was so, what chance was there of the perpetuation of such a variation? On the hypothesis of Natural Selection itself, we must a.s.sume that up to that time the race had been well adapted to the surrounding conditions; the temporary and accidental trial and change of conditions, which caused the so-sucking young one to be the "fittest to survive" under the supposed circ.u.mstances, would soon cease to act, and then the progeny of the mother, with the accidentally hypertrophied, sebaceous glands, would have no tendency to survive the {48} far outnumbering descendants of the normal ancestral form. If, on the other hand, we a.s.sume the change of conditions not to have been temporary but permanent, and also a.s.sume that this permanent change of conditions was accidentally synchronous with the change of structure, we have a coincidence of very remote probability indeed. But if, again, we accept the presence of some harmonizing law simultaneously determining the two changes, or connecting the second with the first by causation, then, of course, we remove the accidental character of the coincidence.

Again, how explain the external position of the male s.e.xual glands in certain mammals? The utility of the modification, when accomplished, is problematical enough, and no less so the incipient stages of the descent.

As was said in the first chapter, Mr. Darwin explains the brilliant plumage of the peac.o.c.k or the humming-bird by the action of s.e.xual selection: the more and more brilliant males being selected by the females (which are thus attracted) to become the fathers of the next generation, to which generation they tend to communicate their own bright nuptial vesture. But there are peculiarities of colour and of form which it is exceedingly difficult to account for by any such action. Thus, amongst apes, the female is notoriously weaker, and is armed with much less powerful canine tusks than the male. When we consider what is known of the emotional nature of these animals, and the periodicity of its intensification, it is hardly credible that a female would often risk life or limb through her admiration of a trifling shade of colour, or an infinitesimally greater though irresistibly fascinating degree of wartiness.[38]

{49} [Ill.u.s.tration: RATTLESNAKE.]

Yet the males of some kinds of ape are adorned with quite exceptionally brilliant local decoration, and the male orang is provided with remarkable, projecting, warty lumps of skin upon the cheeks. As we have said, the weaker female can hardly be supposed to have developed these by persevering and long-continued selection, nor can they be thought to tend to the preservation of the individual. On the contrary, the presence of this enlarged appendage must occasion a slight increase in the need of nutriment, and in so far must be a detriment, although its detrimental effect would not be worth speaking of except in relation to "Darwinism,"

according to which, "selection" has acted through unimaginable ages, {50} and has ever tended to suppress any useless development by the struggle for life.[39]

[Ill.u.s.tration: COBRA.

(_Copied, by permission, from Sir Andrew Smith's "Reptiles of South Africa."_)]

In poisonous serpents, also, we have structures which, at all events at first sight, seem positively hurtful to those reptiles. Such are the rattle of the rattlesnake, and the expanding neck of the cobra, the former seeming to warn the ear of the intended victim, as the latter warns the eye. It is true we cannot perhaps demonstrate that the victims are alarmed and warned, but, on Darwinian principles, they certainly ought to be so. For the {51} rashest and most incautious of the animals preyed on would always tend to fall victims, and the existing individuals being the long-descended progeny of the timid and cautious, ought to have an inherited tendency to distrust, amongst other things, both "rattling" and "expanding" snakes. As to any power of fascination exercised by means of these actions, the most distinguished naturalists, certainly the most distinguished erpetologists, entirely deny it, and it is opposed to the careful observations of those known to us.[40]

The mode of formation of both the eye and the ear of the highest animals is such that, if it is (as most Darwinians a.s.sert processes of development to be) a record of the actual steps by which such structures were first evolved in antecedent forms, it almost amounts to a demonstration that those steps were never produced by "Natural Selection."

The eye is formed by a simultaneous and corresponding ingrowth of one part and outgrowth of another. The skin in front of the future eye becomes depressed, the depression increases and a.s.sumes the form of a sac, which changes into the aqueous humour and lens. An outgrowth of brain substance, on the other hand, forms the retina, while a third process is a lateral ingrowth of connective tissue, which afterwards changes into the vitreous humour of the eye.

The internal ear is formed by an involution of the integument, and not by an outgrowth of the brain. But tissue, in connexion with it, becomes in part changed, thus forming the auditory nerve, which places the tegumentary sac in direct communication with the brain itself.

{52} Now, these complex and simultaneous co-ordinations could never have been produced by infinitesimal beginnings, since, until so far developed as to effect the requisite junctions, they are useless. But the eye and ear when fully developed present conditions which are hopelessly difficult to reconcile with the mere action of "Natural Selection." The difficulties with regard to the eye have been well put by Mr. Murphy, especially that of the concordant result of visual development springing from different starting-points and continued on by independent roads.

He says,[41] speaking of the beautiful structure of the perfect eye, "The higher the organization, whether of an entire organism or of a single organ, the greater is the number of the parts that co-operate, and the more perfect is their co-operation; and consequently, the more necessity there is for corresponding variations to take place in all the co-operating parts at once, and the more useless will be any variation whatever unless it is accompanied by corresponding variations in the co-operating parts; while it is obvious that the greater the number of variations which are needed in order to effect an improvement, the less will be the probability of their all occurring at once. It is no reply to this to say, what is no doubt abstractedly true, that whatever is possible becomes probable, if only time enough be allowed. There are improbabilities so great that the common sense of mankind treats them as impossibilities. It is not, for instance, in the strictest sense of the word, impossible that a poem and a mathematical proposition should be obtained by the process of shaking letters out of a box; but it is improbable to a degree that cannot be distinguished from impossibility; and the improbability of obtaining an improvement in an organ by means of several spontaneous variations, all occurring together, is an improbability of the same kind. If we suppose that any single variation occurs on the average once in _m_ times, the probability of {53} that variation occurring in any individual will be

1/_m_;

and suppose that _x_ variations must concur in order to make an improvement, then the probability of the necessary variations all occurring together will be

1/_m_^x.