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-passage 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 passes over the opening, but is prevented from falling into it (and thus causing death from choking) by the action of a small cartilaginous shield (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 passage, and is thus enabled to give free entrance to the air for the lungs, while the milk passes 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!



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 class (Echinodermata), the species of which possess generally spheroidal bodies, built up of multitudinous calcareous plates, and constitute 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.



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 class of insects, and inside that class 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 accumulation 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 assigned 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 assume 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 circumstances, 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 assume the change of conditions not to have been temporary but permanent, and also assume 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 sexual 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 peacock or the humming-bird by the action of sexual 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}

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]



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 assert 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 assumes 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.

Now suppose, what I think a moderate proposition, that the value of m is 1,000, and the value of x is 10, then

1/m^x = 1/1000^{10} = 1/10^{30}.

A number about ten thousand times as great as the number of waves of light that have fallen on the earth since historical time began. And it is to be further observed, that no improvement will give its possessor a certainty of surviving and leaving offspring, but only an extra chance, the value of which it is quite impossible to estimate." This difficulty is, as Mr. Murphy points out, greatly intensified by the undoubted fact that the wonderfully complex structure has been arrived at quite independently in beasts on the one hand and in cuttle-fishes on the other; while creatures of the insect and crab division present us with a third and quite separately developed complexity.

As to the ear, it would take up too much space to describe its internal structure;[42] it must suffice to say that in its interior there is an immense series of minute rod-like bodies, termed fibres of Corti, having the appearance of a key-board, and each fibre being connected with a filament of the auditory nerve, these nerves being like strings to be struck by the keys, i.e. by the fibres of Corti. Moreover, this apparatus is supposed to be a key-board in function as well as in appearance, the{54} vibration of each one fibre giving rise, it is believed, to the sensation of one particular tone, and combinations of such vibrations producing chords. It is by the action of this complex organ then, that all the wonderful intricacy and beauty of Beethoven and Mozart come, most probably, to be perceived and appreciated.

Now it can hardly be contended that the preservation of any race of men in the struggle for life ever depended on such an extreme delicacy and refinement of the internal ear,—a perfection only exercised in the enjoyment and appreciation of the most perfect musical performances. How, then, could either the minute incipient stages, or the final perfecting touches of this admirable structure, have been brought about by vague, aimless, and indefinite variations in all conceivable directions of an organ, suitable to enable the rudest savage to minister to his necessities, but no more?

Mr. Wallace[43] makes an analogous remark with regard to the organ of voice in man—the human larynx. He says of singing: "The habits of savages give no indication of how this faculty could have been developed by Natural Selection, because it is never required or used by them. The singing of savages is a more or less monotonous howling, and the females seldom sing at all. Savages certainly never choose their wives for fine voices, but for rude health, and strength, and physical beauty. Sexual selection could not therefore have developed this wonderful power, which only comes into play among civilized people."

Reverting once more to beauty of form and colour, there is one manifestation of it for which no one can pretend that sexual selection can possibly account. The instance referred to is that presented by bivalve shell-fish.[44] Here we meet with charming tints and elegant forms and markings of no direct use to their possessors[45] in the struggle for {55} life, and of no indirect utility as regards sexual selection, for fertilization takes place by the mere action of currents of water, and the least beautiful individual has fully as good a chance of becoming a parent as has the one which is the most favoured in beauty of form and colour.

Again, the peculiar outline and coloration of certain orchids—notably of our own bee, fly, and spider orchids—seem hardly explicable by any action of "Natural Selection." Mr. Darwin says very little on this singular resemblance of flowers to insects, and what he does say seems hardly to be what an advocate of "Natural Selection" would require. Surely, for minute accidental indefinite variations to have built up such a striking resemblance to insects, we ought to find that the preservation of the plant, or the perpetuation of its race, depends almost constantly on relations between bees, spiders, and flies respectively and the bee, spider, and fly orchids.[46] This process must have continued for ages constantly and perseveringly, and yet what is the fact? Mr. Darwin tells us, in his work on the Fertilization of Orchids, that neither the spider nor the fly orchids are much visited by insects, while, with regard to the bee orchid, he says, "I have never seen an insect visit these flowers." And he shows how this species is even wonderfully and specially modified to effect self-fertilization.

In the work just referred to Mr. Darwin gives a series of the most wonderful and minute contrivances by which the visits of insects are utilized for the fertilization of orchids,—structures so wonderful {56} that nothing could well be more so, except the attribution of their origin to minute, fortuitous, and indefinite variation.

The instances are too numerous and too long to quote, but in his "Origin of Species"[47] he describes two which must not be passed over. In one (Coryanthes) the orchid has its lower lip enlarged into a bucket, above which stand two water-secreting horns. These latter replenish the bucket from which, when half-filled, the water overflows by a spout on one side. Bees visiting the flower fall into the bucket and crawl out at the spout. By the peculiar arrangement of the parts of the flower, the first bee which does so carries away the pollen-mass glued to his back, and then when he has his next involuntary bath in another flower, as he crawls out the pollen-mass attached to him comes in contact with the stigma of that second flower and fertilizes it. In the other example (Catasetum), when a bee gnaws a certain part of the flower, he inevitably touches a long delicate projection, which Mr. Darwin calls the antenna. "This antenna transmits a vibration to a certain membrane, which is instantly ruptured; this sets free a spring by which the pollen-mass is shot forth like an arrow in the right direction, and adheres by its viscid extremity to the back of the bee!"

Another difficulty, and one of some importance, is presented by those communities of ants which have not only a population of sterile females, or workers, but two distinct and very different castes of such. Mr. Darwin believes that he has got over this difficulty by having found individuals intermediate in form and structure[48] between the two working castes; others may think that we have in this belief of Mr. Darwin, an example {57} of the unconscious action of volition upon credence. A vast number of difficulties similar to those which have been mentioned might easily be cited—those given, however, may suffice.

There remains, however, to be noticed a very important consideration, which was brought forward in the North British Review for June 1867, p. 286, namely, the necessity for the simultaneous modification of many individuals. This consideration seems to have escaped Mr. Darwin, for at p. 104 of his last (fifth) edition of "Natural Selection," he admits, with great candour, that until reading this article he did not "appreciate how rarely single variations, whether slight or strongly marked, could be perpetuated."

The North British Review (speaking of the supposition that a species is changed by the survival of a few individuals in a century through a similar and favourable variation) says: "It is very difficult to see how this can be accomplished, even when the variation is eminently favourable indeed; and still more difficult when the advantage gained is very slight, as must generally be the case. The advantage, whatever it may be, is utterly outbalanced by numerical inferiority. A million creatures are born; ten thousand survive to produce offspring. One of the million has twice as good a chance as any other of surviving; but the chances are fifty to one against the gifted individuals being one of the hundred survivors. No doubt the chances are twice as great against any one other individual, but this does not prevent their being enormously in favour of some average individual. However slight the advantage may be, if it is shared by half the individuals produced, it will probably be present in at least fifty-one of the survivors, and in a larger proportion of their offspring; but the chances are against the preservation of any one 'sport' (i.e. sudden, marked variation) in a numerous tribe. The vague use of an imperfectly understood doctrine of chance has led Darwinian supporters, first, to confuse the two cases above distinguished; and, secondly, to imagine {58} that a very slight balance in favour of some individual sport must lead to its perpetuation. All that can be said is that in the above example the favoured sport would be preserved once in fifty times. Let us consider what will be its influence on the main stock when preserved. It will breed and have a progeny of say 100; now this progeny will, on the whole, be intermediate between the average individual and the sport. The odds in favour of one of this generation of the new breed will be, say one and a half to one, as compared with the average individual; the odds in their favour will, therefore, be less than that of their parents; but owing to their greater number, the chances are that about one and a half of them would survive. Unless these breed together, a most improbable event, their progeny would again approach the average individual; there would be 150 of them, and their superiority would be, say in the ratio of one and a quarter to one; the probability would now be that nearly two of them would survive, and have 200 children, with an eighth superiority. Rather more than two of these would survive; but the superiority would again dwindle, until after a few generations it would no longer be observed, and would count for no more in the struggle for life than any of the hundred trifling advantages which occur in the ordinary organs. An illustration will bring this conception home. Suppose a white man to have been wrecked on an island inhabited by negroes, and to have established himself in friendly relations with a powerful tribe, whose customs he has learnt. Suppose him to possess the physical strength, energy, and ability of a dominant white race, and let the food and climate of the island suit his constitution; grant him every advantage which we can conceive a white to possess over the native; concede that in the struggle for existence his chance of a long life will be much superior to that of the native chiefs; yet from all these admissions, there does not follow the conclusion that, after a limited or unlimited {59} number of generations, the inhabitants of the island will be white. Our shipwrecked hero would probably become king; he would kill a great many blacks in the struggle for existence; he would have a great many wives and children." ... "In the first generation there will be some dozens of intelligent young mulattoes, much superior in average intelligence to the negroes. We might expect the throne for some generations to be occupied by a more or less yellow king; but can any one believe that the whole island will gradually acquire a white, or even a yellow, population?"

"Darwin says that in the struggle for life a grain may turn the balance in favour of a given structure, which will then be preserved. But one of the weights in the scale of nature is due to the number of a given tribe. Let there be 7000 A's and 7000 B's, representing two varieties of a given animal, and let all the B's, in virtue of a slight difference of structure, have the better chance of life by 1/7000 part. We must allow that there is a slight probability that the descendants of B will supplant the descendants of A; but let there be only 7001 A's against 7000 B's at first, and the chances are once more equal, while if there be 7002 A's to start, the odds would be laid on the A's. True, they stand a greater chance of being killed; but then they can better afford to be killed. The grain will only turn the scales when these are very nicely balanced, and an advantage in numbers counts for weight, even as an advantage in structure. As the numbers of the favoured variety diminish, so must its relative advantages increase, if the chance of its existence is to surpass the chance of its extinction, until hardly any conceivable advantage would enable the descendants of a single pair to exterminate the descendants of many thousands if they and their descendants are supposed to breed freely with the inferior variety, and so gradually lose their ascendency."

Mr. Darwin himself says of the article quoted: "The justice of these remarks cannot, I think, be disputed. If, for instance, a bird of some {60} kind could procure its food more easily by having its beak curved, and if one were born with its beak strongly curved, and which consequently flourished, nevertheless there would be a very poor chance of this one individual perpetuating its kind to the exclusion of the common form." This admission seems almost to amount to a change of front in the face of the enemy!

These remarks have been quoted at length because they so greatly intensify the difficulties brought forward in this chapter. If the most favourable variations have to contend with such difficulties, what must be thought as to the chance of preservation of the slightly displaced eye in a sole or of the incipient development of baleen in a whale?

SUMMARY AND CONCLUSION.

It has been here contended that a certain few facts, out of many which might have been brought forward, are inconsistent with the origination of species by "Natural Selection" only or mainly.

Mr. Darwin's theory requires minute, indefinite, fortuitous variations of all parts in all directions, and he insists that the sole operation of "Natural Selection" upon such is sufficient to account for the great majority of organic forms, with their most complicated structures, intricate mutual adaptations and delicate adjustments.

To this conception has been opposed the difficulties presented by such a structure as the form of the giraffe, which ought not to have been the solitary structure it is; also the minute beginnings and the last refinements of protective mimicry equally difficult or rather impossible to account for by "Natural Selection." Again the difficulty as to the heads of flat-fishes has been insisted on, as also the origin, and at the same time the constancy, of the limbs of the highest animals. Reference has also been made to the whalebone of whales, and to the impossibility of {61} understanding its origin through "Natural Selection" only; the same as regards the infant kangaroo, with its singular deficiency of power compensated for by maternal structures on the one hand, to which its own breathing organs bear direct relation on the other. Again, the delicate and complex pedicellariae of Echinoderms, with a certain process of development (through a secondary larva) found in that class, together with certain other exceptional modes of development, have been brought forward. The development of colour in certain apes, the hood of the cobra, and the rattle of the rattlesnake have also been cited. Again, difficulties as to the process of formation of the eye and ear, and as to the fully developed condition of those complex organs, as well as of the voice, have been considered. The beauty of certain shell-fish; the wonderful adaptations of structure, and variety of form and resemblance, found in orchids; together with the complex habits and social conditions of certain ants, have been hastily passed in review. When all these complications are duly weighed and considered, and when it is borne in mind how necessary it is for the permanence of a new variety that many individuals in each case should be simultaneously modified, the cumulative argument seems irresistible.

The Author of this book can say that though by no means disposed originally to dissent from the theory of "Natural Selection," if only its difficulties could be solved, he has found each successive year that deeper consideration and more careful examination have more and more brought home to him the inadequacy of Mr. Darwin's theory to account for the preservation and intensification of incipient, specific, and generic characters. That minute, fortuitous, and indefinite variations could have brought about such special forms and modifications as have been enumerated in this chapter, seems to contradict not imagination, but reason. [Page 62]

That either many individuals amongst a species of butterfly should be simultaneously preserved through a similar accidental and minute variation in one definite direction, when variations in many other directions would also preserve; or that one or two so varying should succeed in supplanting the progeny of thousands of other individuals, and that this should by no other cause be carried so far as to produce the appearance (as we have before stated) of spots of fungi, &c.—are alternatives of an improbability so extreme as to be practically equal to impossibility.

In spite of all the resources of a fertile imagination, the Darwinian, pure and simple, is reduced to the assertion of a paradox as great as any he opposes. In the place of a mere assertion of our ignorance as to the way these phenomena have been produced, he brings forward, as their explanation, a cause which it is contended in this work is demonstrably insufficient.

Of course in this matter, as elsewhere throughout nature, we have to do with the operation of fixed and constant natural laws, and the knowledge of these may before long be obtained by human patience or human genius; but there is, it is believed, already enough evidence to show that these as yet unknown natural laws or law will never be resolved into the action of "Natural Selection," but will constitute or exemplify a mode and condition of organic action of which the Darwinian theory takes no account whatsoever. [Page 63]

* * * * *

CHAPTER III.

THE CO-EXISTENCE OF CLOSELY SIMILAR STRUCTURES OF DIVERSE ORIGIN.

Chances against concordant variations.—Examples of discordant ones.—Concordant variations not unlikely on a non-Darwinian evolutionary hypothesis.—Placental and implacental mammals.—Birds and reptiles.—Independent origins of similar sense organs.—The ear.—The eye.—Other coincidences.—Causes besides Natural Selection produce concordant variations in certain geographical regions.—Causes besides Natural Selection produce concordant variations in certain zoological and botanical groups.—There are homologous parts not genetically related.—Harmony in respect of the organic and inorganic worlds.—Summary and conclusion.

The theory of "Natural Selection" supposes that the varied forms and structure of animals and plants have been built up merely by indefinite, fortuitous,[49] minute variations in every part and in all directions—those variations only being preserved which are directly or indirectly useful to the individual possessing them, or necessarily correlated with such useful variations.



On this theory the chances are almost infinitely great against the independent, accidental occurrence and preservation of two similar series of minute variations resulting in the independent development of two closely similar forms. In all cases, no doubt (on this same theory), some adaptation to habit or need would gradually be evolved, but that {64} adaptation would surely be arrived at by different roads. The organic world supplies us with multitudes of examples of similar functional results being attained by the most diverse means. Thus the body is sustained in the air by birds and by bats. In the first case it is so sustained by a limb in which the bones of the hand are excessively reduced, but which is provided with immense outgrowths from the skin—namely, the feathers of the wing. In the second case, however, the body is sustained in the air by a limb in which the bones of the hand are enormously increased in length, and so sustain a great expanse of naked skin, which is the flying membrane of the bat's wing. Certain fishes and certain reptiles can also flit and take very prolonged jumps in the air. The flying-fish, however, takes these by means of a great elongation of the rays of the pectoral fins—parts which cannot be said to be of the same nature as the constituents of the wing of either the bat or the bird. The little lizard, which enjoys the formidable name of "flying-dragon," flits by means of a structure altogether peculiar—namely, by the liberation and great elongation of some of the ribs which support a fold of skin. In the extinct pterodactyles—which were truly flying {65} reptiles—we meet with an approximation to the structure of the bat, but in the pterodactyle we have only one finger elongated in each hand: a striking example of how the very same function may be provided for by a modification similar in principle, yet surely manifesting the independence of its origin. When we go to lower animals, we find flight produced by organs, as the wings of insects, which are not even modified limbs at all; or we find even the function sometimes subserved by quite artificial means, as in the aerial spiders, which use their own threads to float with in the air. In the vegetable kingdom the atmosphere is often made use of for the scattering of seeds, by their being furnished with special structures of very different kinds. The diverse modes by which such seeds are dispersed are well expressed by Mr. Darwin. He says:[50] "Seeds are disseminated {66} by their minuteness,—by their capsule being converted into a light balloon-like envelope,—by being embedded in pulp or flesh, formed of the most diverse parts, and rendered nutritious, as well as conspicuously coloured, so as to attract and be devoured by birds,—by having hooks and grapnels of many kinds and serrated awns, so as to adhere to the fur of quadrupeds,—and by being furnished with wings and plumes, as different in shape as elegant in structure, so as to be wafted by every breeze."



Again, if we consider the poisoning apparatus possessed by different animals, we find in serpents a perforated—or rather very deeply channelled—tooth. In wasps and bees the sting is formed of modified parts, accessory in reproduction. In the scorpion, we have the median terminal process of the body specially organized. In the spider, we have a specially constructed antenna; and finally in the centipede a pair of modified thoracic limbs.



It would be easy to produce a multitude of such instances of similar ends being attained by dissimilar means, and it is here contended that by "the action of Natural Selection" only it is so improbable as to be practically impossible for two exactly similar structures to have ever been independently developed. It is so because the number of possible {67} variations is indefinitely great, and it is therefore an indefinitely great number to one against a similar series of variations occurring and being similarly preserved in any two independent instances.

The difficulty here asserted applies, however, only to pure Darwinism, which makes use only of indirect modifications through the survival of the fittest.

Other theories (for example, that of Mr. Herbert Spencer) admit the direct action of conditions upon animals and plants—in ways not yet fully understood—there being conceived to be at the same time a certain peculiar but limited power of response and adaptation in each animal and plant so acted on. Such theories have not to contend against the difficulty proposed, and it is here urged that even very complex extremely similar structures have again and again been developed quite independently one of the other, and this because the process has taken place not by merely haphazard, indefinite variations in all directions, but by the concurrence of some other and internal natural law or laws co-operating with external influences and with Natural Selection in the evolution of organic forms.

It must never be forgotten that to admit any such constant operation of any such unknown natural cause is to deny the purely Darwinian theory, which relies upon the survival of the fittest by means of minute fortuitous indefinite variations.

Amongst many other obligations which the Author has to acknowledge to Professor Huxley, are the pointing out of this very difficulty, and the calling his attention to the striking resemblance between certain teeth of the dog and of the thylacine as one instance, and certain ornithic peculiarities of pterodactyles as another.

Mammals[51] are divisible into one great group, which comprises the {68} immense majority of kinds termed, from their mode of reproduction, placental Mammals, and into another very much smaller group comprising the pouched-beasts or marsupials (which are the kangaroos, bandicoots, phalangers, &c., of Australia), and the true opossums of America, called implacental Mammals. Now the placental mammals are subdivided into various orders, amongst which are the flesh-eaters (Carnivora, i.e. cats, dogs, otters, weasels, &c.), and the insect-eaters (Insectivora, i.e. moles, hedgehogs, shrew-mice, &c.). The marsupial mammals also present a variety of forms (some of which are carnivorous beasts, whilst others are insectivorous), so marked that it has been even proposed to divide them into orders parallel to the orders of placental beasts.

The resemblance, indeed, is so striking as, on Darwinian principles, to suggest the probability of genetic affinity; and it even led Professor Huxley, in his Hunterian Lectures, in 1866, to promulgate the notion that a vast and widely-diffused marsupial fauna may have existed anteriorly to the development of the ordinary placental, non-pouched beasts, and that the carnivorous, insectivorous, and herbivorous placentals may have respectively descended from the carnivorous, insectivorous, and herbivorous marsupials.



Amongst other points Professor Huxley called attention to the resemblance between the anterior molars of the placental dog with those of the marsupial thylacine. These, indeed, are strikingly similar, but there are better examples still of this sort of coincidence. Thus it has often {69} been remarked that the insectivorous marsupials, e.g. Perameles, wonderfully correspond, as to the form of certain of the grinding teeth, with certain insectivorous placentals, e.g. Urotrichus.

Again, the saltatory insectivores of Africa (Macroscelides) not only resemble the kangaroo family (Macropodidae) in their jumping habits and long hind legs, but also in the structure of their molar teeth, and even further, as I have elsewhere[52] pointed out, in a certain similarity of the upper cutting teeth, or incisors.

Now these correspondences are the more striking when we bear in mind that a similar dentition is often put to very different uses. The food of different kinds of apes is very different, yet how uniform is their dental structure! Again, who, looking at the teeth of different kinds of bears, would ever suspect that one kind was frugivorous, and another a devourer exclusively of animal food?

The suggestion made by Professor Huxley was therefore one which had much to recommend it to Darwinians, though it has not met with any notable acceptance, and though he seems himself to have returned to the older notion, namely, that the pouched-beasts, or marsupials, are a special ancient offshoot from the great mammalian class.

But whichever view may be the correct one, we have in either case a number of forms similarly modified in harmony with surrounding conditions, and eloquently proclaiming some natural plastic power, other than mere fortuitous variation with survival of the fittest. If, however, the Reader thinks that teeth are parts peculiarly qualified for rapid variation (in which view the Author cannot concur), he is requested to suspend his judgment till he has considered the question of the independent evolution of the highest organs of sense. If this seems to establish the {70} existence of some other law than that of "Natural Selection," then the operation of that other law may surely be also traced in the harmonious co-ordinations of dental form.

The other difficulty, kindly suggested to me by the learned Professor, refers to the structure of birds, and of extinct reptiles more or less related to them.

The class of birds is one which is remarkably uniform in its organization. So much is this the case, that the best mode of subdividing the class is a problem of the greatest difficulty. Existing birds, however, present forms which, though closely resembling in the greater part of their structure, yet differ importantly the one from the other. One form is exemplified by the ostrich, rhea, emeu, cassowary, apteryx, dinornis, &c. These are the struthious birds. All other existing birds belong to the second division, and are called (from the keel on the breast-bone) carinate birds.

Now birds and reptiles have such and so many points in common, that Darwinians must regard the former as modified descendants of ancient reptilian forms. But on Darwinian principles it is impossible that the class of birds so uniform and homogeneous should have had a double reptilian origin. If one set of birds sprang from one set of reptiles, and another set of birds from another set of reptiles, the two sets could never, by "Natural Selection" only, have grown into such a perfect similarity. To admit such a phenomenon would be equivalent to abandoning the theory of "Natural Selection" as the sole origin of species.

Now, until recently it has generally been supposed by evolutionists that those ancient flying reptiles, the pterodactyles, or forms allied to them, were the progenitors of the class of birds; and certain parts of their structure especially support this view. Allusion is here made to the bladebone (scapula), and the bone which passes down from the shoulder-joint to the breast-bone (viz. the coracoid). These bones are such remarkable anticipations of the same parts in ordinary (i.e. carinate) birds {71} that it is hardly possible for a Darwinian not to regard the resemblance as due to community of origin. This resemblance was carefully pointed out by Professor Huxley in his "Hunterian Course" for 1867, when attention was called to the existence in Dimorphodon macronyx of even that small process which in birds gives attachment to the upper end of the merrythought. Also Mr. Seeley[53] has shown that in pterodactyles, as in birds, the optic lobes of the brain were placed low down on each side—"lateral and depressed." Nevertheless, the view has been put forward and ably maintained by the same Professor,[54] as also by Professor Cope in the United States, that the line of descent from reptiles to birds has not been from ordinary reptiles, through pterodactyle-like forms, to ordinary birds, but to the struthious ones from certain extinct reptiles termed Dinosauria; one of the most familiarly known of which is the Iguanodon of the Wealden formation. In these Dinosauria we find skeletal characters unlike those of ordinary (i.e. carinate) birds, but closely resembling in certain points the osseous structure of the struthious birds. Thus a difficulty presents itself as to the explanation of the three following relationships:—(1) That of the Pterodactyles with carinate birds; (2) that of the Dinosauria with struthious birds; (3) that of the carinate and struthious birds with each other.

Either birds must have had two distinct origins whence they grew to their present conformity, or the very same skeletal, and probably cerebral characters must have spontaneously and independently arisen. Here is a dilemma, either horn of which bears a threatening aspect to the exclusive supporter of "Natural Selection," and between which it seems somewhat {72} difficult to choose.

It has been suggested to me that this difficulty may be evaded by considering pterodactyles and carinate birds as independent branches from one side of an ancient common trunk, while similarly the Dinosauria and struthious birds are taken to be independent branches from the other side of the same common trunk; the two kinds of birds resembling each other so much on account of their later development from that trunk as compared with the development of the reptilian forms. But to this it may be replied that the ancient common stock could not have had at one and the same time a shoulder structure of both kinds. It must have been that of the struthious birds or that of the carinate birds, or something different from both. If it was that of the struthious birds, how did the pterodactyles and carinate birds independently arrive at the very same divergent structure? If it was that of the carinate birds, how did the struthious birds and Dinosauria independently agree to differ? Finally, if it was something different from either, how did the carinate birds and pterodactyles take on independently one special common structure when disagreeing in so many; while the struthious birds, agreeing in many points with the Dinosauria, agree yet more with the carinate birds? Indeed by no arrangement of branches from a stem can the difficulty be evaded.

Professor Huxley seems inclined[55] to cut the Gordian knot by considering the shoulder structure of the pterodactyle as independently educed, and having relation to physiology only. This conception is one which harmonizes completely with the views here advocated, and with those of Mr. Herbert Spencer, who also calls in direct modification to the aid of "Natural Selection." That merely minute, indefinite variations in all directions should unaided have independently built up the shoulder structure of {73} the pterodactyles and carinate birds, and have laterally depressed their optic lobes, at a time so far back as the deposition of the Oolite strata,[56] is a coincidence of the highest improbability; but that an innate power and evolutionary law, aided by the corrective action of "Natural Selection," should have furnished like needs with like aids, is not at all improbable. The difficulty does not tell against the theory of evolution, but only against the specially Darwinian form of it. Now this form has never been expressly adopted by Professor Huxley; so far from it, in his lecture on this subject at the Royal Institution before referred to, he observes,[57] "I can testify, from personal experience, it is possible to have a complete faith in the general doctrine of evolution, and yet to hesitate in accepting the Nebular, or the Uniformitarian, or the Darwinian hypotheses in all their integrity and fulness."



It is quite consistent, then, in the Professor to explain the {74} difficulty as he does; but it would not be similarly so with an absolute and pure Darwinian.

Yet stronger arguments of an analogous kind are, however, to be derived from the highest organs of sense. In the most perfectly organized animals—those namely which, like ourselves, possess a spinal column—the internal organs of hearing consist of two more or less complex membranous sacs (containing calcareous particles—otoliths), which are primitively or permanently lodged in two chambers, one on each side of the cartilaginous skull. The primitive cartilaginous cranium supports and protects the base of the brain, and the auditory nerves pass from that brain into the cartilaginous chambers to reach the auditory sacs. These complex arrangements of parts could not have been evolved by "Natural Selection," i.e. by minute accidental variations, except by the action of such through a vast period of time; nevertheless, it was fully evolved at the time of the deposition of the upper Silurian rocks.

Cuttle-fishes (Cephalopoda) are animals belonging to the molluscous primary division of the animal kingdom, which division contains animals formed upon a type of structure utterly remote from that on which the animals of the higher division provided with a spinal column are constructed. And indeed no transitional form (tending even to bridge over the chasm between these two groups) has ever yet been discovered, either living or in a fossilized condition.[58]

Nevertheless, in the two-gilled Cephalopods (Dibranchiata) we find the brain supported and protected by a cartilaginous cranium. In the base of this cranium are two cartilaginous chambers. In each chamber is a membranous sac containing an otolith, and the auditory nerves pass from the cerebral ganglia into the cartilaginous chambers to reach the auditory sacs. Moreover, it has been suggested by Professor Owen that {75} sinuosities between processes projecting from the inner wall of each chamber "seem to be the first rudiments of those which, in the higher classes (i.e. in animals with a spinal column), are extended in the form of canals and spiral chambers, within the substance of the dense nidus of the labyrinth."[59]



Here, then, we have a wonderful coincidence indeed; two highly complex auditory organs, marvellously similar in structure, but which must nevertheless have been developed in entire and complete independence one of the other! It would be difficult to calculate the odds against the independent occurrence and conservation of two such complex series of merely accidental and minute haphazard variations. And it can never be {76} maintained that the sense of hearing could not be efficiently subserved otherwise than by such sacs, in cranial cartilaginous capsules so situated in relation to the brain, &c.

Our wonder, moreover, may be increased when we recollect that the two-gilled cephalopods have not yet been found below the lias, where they at once abound; whereas the four-gilled cephalopods are Silurian forms. Moreover, the absence is in this case significant in spite of the imperfection of the geological record, because when we consider how many individuals of various kinds of four-gilled cephalopods have been found, it is fair to infer that at the least a certain small percentage of dibranchs would also have left traces of their presence had they existed. Thus it is probable that some four-gilled form was the progenitor of the dibranch cephalopods. Now the four-gilled kinds (judging from the only existing form, the nautilus) had the auditory organ in a very inferior condition of development to what we find in the dibranch; thus we have not only evidence of the independent high development of the organ in the former, but also evidence pointing towards a certain degree of comparative rapidity in its development.

Such being the case with regard to the organ of hearing, we have another yet stronger argument with regard to the organ of sight, as has been well pointed out by Mr. J. J. Murphy.[60] He calls attention to the fact that the eye must have been perfected in at least "three distinct lines of descent," alluding not only to the molluscous division of the animal kingdom, and the division provided with a spinal column, but also to a third primary division, namely, that which includes all insects, spiders, crabs, &c., which are spoken of as Annulosa, and the type of whose structure is as distinct from that of the molluscous type on the one hand, as it is from that of the type with a spinal column (i.e. the vertebrate type) on the other.

{77} In the cuttle-fishes we find an eye even more completely constructed on the vertebrate type than is the ear. Sclerotic, retina, choroid, vitreous humour, lens, aqueous humour, all are present. The correspondence is wonderfully complete, and there can hardly be any hesitation in saying that for such an exact, prolonged, and correlated series of similar structures to have been brought about in two independent instances by merely indefinite and minute accidental variations, is an improbability which amounts practically to impossibility. Moreover, we have here again the same imperfection of the four-gilled cephalopod, as compared with the two-gilled, and therefore (if the latter proceeded from the former) a similar indication of a certain comparative rapidity of development. Finally, and this is perhaps one of the most curious circumstances, the process of formation appears to have been, at least in some respects, the same in the eyes of these molluscous animals as in the eyes of vertebrates. For in these latter the cornea is at first perforated, while different degrees of perforation of the same part are presented by different adult cuttle-fishes—large in the calamaries, smaller in the octopods, and reduced to a minute foramen in the true cuttle-fish sepia.

Some may be disposed to object that the conditions requisite for effecting vision are so rigid that similar results in all cases must be independently arrived at. But to this objection it may well be replied that Nature herself has demonstrated that there is no such necessity as to the details of the process. For in the higher Annulosa, such as the dragon-fly, we meet with an eye of an unquestionably very high degree of efficiency, but formed on a type of structure only remotely comparable with that of the fish or the cephalopod. The last-named animal might have had an eye as efficient as that of a vertebrate, but formed on a distinct type, instead of being another edition, as it were, of the very same structure.

In the beginning of this chapter examples have been given of the very {78} diverse mode in which similar results have in many instances been arrived at; on the other hand, we have in the fish and the cephalopod not only the eye, but at one and the same time the ear also similarly evolved, yet with complete independence.

Thus it is here contended that the similar and complex structures of both the highest organs of sense, as developed in the vertebrates on the one hand, and in the mollusks on the other, present us with residuary phenomena for which "Natural Selection" alone is quite incompetent to account. And that these same phenomena must therefore be considered as conclusive evidence for the action of some other natural law or laws conditioning the simultaneous and independent evolution of these harmonious and concordant adaptations.

Provided with this evidence, it may be now profitable to enumerate other correspondences, which are not perhaps in themselves inexplicable by Natural Selection, but which are more readily to be explained by the action of the unknown law or laws referred to—which action, as its necessity has been demonstrated in one case, becomes a priori probable in the others.



Thus the great oceanic Mammalia—the whales—show striking resemblances to those prodigious, extinct, marine reptiles, the Ichthyosauria, and this not only in structures readily referable to similarity of habit, but in such matters as greatly elongated premaxillary bones, together with the concealment of certain bones of the skull by other cranial bones. [Page 79]

Again, the aerial mammals, the bats, resemble those flying reptiles of the secondary epoch, the pterodactyles; not only to a certain extent in the breast-bone and mode of supporting the flying membrane, but also in the proportions of different parts of the spinal column and the hinder (pelvic) limbs.

Also bivalve shell-fish (i.e. creatures of the mussel, cockle, and oyster class, which receive their name from the body being protected by a double shell, one valve of which is placed on each side) have their two shells united by one or two powerful muscles, which pass directly across from one shell to the other, and which are termed "adductor muscles" because by their contraction they bring together the valves and so close the shell.



Now there are certain animals which belong to the crab and lobster class (Crustacea)—a class constructed on an utterly different type from that on which the bivalve shell-fish are constructed—which present a very curious approximation to both the form and, in a certain respect, the structure of true bivalves. Allusion is here made to certain small Crustacea—certain phyllopods and ostracods—which have the hard outer coat of their thorax so modified as to look wonderfully like a bivalve shell, although its {80} nature and composition are quite different. But this is by no means all,—not only is there this external resemblance between the thoracic armour of the crustacean and the bivalve shell, but the two sides of the ostracod and phyllopod thorax are connected together also by an adductor muscle!



{81} The pedicellariae of the echinus have been already spoken of, and the difficulty as to their origin from minute, fortuitous, indefinite variations has been stated. But structures essentially similar (called avicularia, or "bird's-head processes") are developed from the surface of the compound masses of certain of the highest of the polyp-like animals (viz. the Polyzoa or, as they are sometimes called, the Bryozoa).

These compound animals have scattered over the surface of their bodies minute processes, each of which is like the head of a bird, with an upper and lower beak, the whole supported on a slender neck. The beak opens and shuts at intervals, like the jaws of the pedicellariae of the echinus, and there is altogether, in general principle, a remarkable similarity between the structures. Yet the echinus can have, at the best, none but the most distant genetic relationship with the Polyzoa. We have here again therefore complex and similar organs of diverse and independent origin.



In the highest class of animals (the Mammalia) we have almost always a placental mode of reproduction, i.e. the blood of the foetus is placed in nutritive relation with the blood of the mother by means of vascular prominences. No trace of such a structure exists in any bird or in any reptile, and yet it crops out again in certain sharks. There indeed it might well be supposed to end, but, marvellous as it seems, it reappears in very lowly creatures; namely, in certain of the ascidians, sometimes called tunicaries or sea-squirts. [Page 82]

Now, if we were to concede that the ascidians were the common ancestors[61] of both these sharks and of the higher mammals, we should be little, if any, nearer to an explanation of the phenomenon by means of "Natural Selection," for in the sharks in question the vascular prominences are developed from one foetal structure (the umbilical vesicle), while in the higher mammals they are developed from quite another part, viz. the allantois.



So great, however, is the number of similar, but apparently independent, structures, that we suffer from a perfect embarras de richesses. Thus, for example, we have the convoluted windpipe of the sloth, reminding us{83} of the condition of the windpipe in birds; and in another mammal, allied to the sloth, namely the great ant-eater (Myrmecophaga), we have again an ornithic character in its horny gizzard-like stomach. In man and the highest apes the caecum has a vermiform appendix, as it has also in the wombat!

Also the similar forms presented by the crowns of the teeth in some seals, in certain sharks, and in some extinct Cetacea may be referred to; as also the similarity of the beak in birds, some reptiles, in the tadpole, and cuttle-fishes. As to entire external form, may be adduced the wonderful similarity between a true mouse (Mus delicatulus) and a small marsupial, pointed out by Mr. Andrew Murray in his work on the "Geographical Distribution of Mammals," p. 53, and represented in the frontispiece by figures copied from Gould's "Mammals of Australia;" but instances enough for the present purpose have been already quoted.

Additional reasons for believing that similarity of structure is produced by other causes than merely by "Natural Selection" are furnished by certain facts of zoological geography, and by a similarity in the mode of variation being sometimes extended to several species of a genus, or even to widely different groups; while the restriction and the limitation of such similarity are often not less remarkable. Thus Mr. Wallace says,[62] as to local influence: "Larger or smaller districts, or even single islands, give a special character to the majority of their Papilionidae. For instance:—1. The species of the Indian region (Sumatra, Java, and Borneo) are almost invariably smaller than the allied species inhabiting Celebes and the Moluccas. 2. The species of New Guinea and Australia are also, though in a less degree, smaller than the nearest species or varieties of the Moluccas. 3. In the Moluccas themselves the species of Amboyna are the largest. 4. The species of Celebes equal or even surpass in size those of Amboyna. {84} 5. The species and varieties of Celebes possess a striking character in the form of the anterior wings, different from that of the allied species and varieties of all the surrounding islands. 6. Tailed species in India or the Indian region become tailless as they spread eastward through the Archipelago. 7. In Amboyna and Ceram the females of several species are dull-coloured, while in the adjacent islands they are more brilliant." Again:[63] "In Amboyna and Ceram the female of the large and handsome Ornithoptera Helena has the large patch on the hind wings constantly of a pale dull ochre or buff colour; while in the scarcely distinguishable varieties from the adjacent islands, of Bouru and New Guinea, it is of a golden yellow, hardly inferior in brilliancy to its colour in the male sex. The female of Ornithoptera Priamus (inhabiting Amboyna and Ceram exclusively) is of a pale dusky brown tint, while in all the allied species the same sex is nearly black, with contracted white markings. As a third example, the female of Papilio Ulysses has the blue colour obscured by dull and dusky tints, while in the closely allied species from the surrounding islands, the females are of almost as brilliant an azure blue as the males. A parallel case to this is the occurrence, in the small islands of Goram, Matabello, Ke, and Aru, of several distinct species of Euploea and Diadema, having broad bands or patches of white, which do not exist in any of the allied species from the larger islands. These facts seem to indicate some local influence in modifying colour, as unintelligible and almost as remarkable as that which has resulted in the modifications of form previously described."

After endeavouring to explain some of the facts in a way to be noticed directly, Mr. Wallace adds:[64] "But even the conjectural explanation now given fails us in the other cases of local modification. Why the species of the Western Islands should be smaller than those further east; why those of Amboyna should exceed in size those of Gilolo and New Guinea; why the {85} tailed species of India should begin to lose that appendage in the islands, and retain no trace of it on the borders of the Pacific; and why, in three separate cases, the females of Amboyna species should be less gaily attired than the corresponding females of the surrounding islands, are questions which we cannot at present attempt to answer. That they depend, however, on some general principle is certain, because analogous facts have been observed in other parts of the world. Mr. Bates informs me that, in three distinct groups, Papilios, which, on the Upper Amazon, and in most other parts of South America, have spotless upper wings, obtain pale or white spots at Para and on the Lower Amazon, and also that the AEneas group of Papilios never have tails in the equatorial regions and the Amazon valley, but gradually acquire tails in many cases as they range towards the northern or southern tropic. Even in Europe we have somewhat similar facts, for the species and varieties of butterflies peculiar to the Island of Sardinia are generally smaller and more deeply coloured than those of the mainland, and the same has been recently shown to be the case with the common tortoiseshell butterfly in the Isle of Man; while Papilio Hospiton, peculiar to the former island, has lost the tail, which is a prominent feature of the closely allied P. Machaon.

"Facts of a similar nature to those now brought forward would no doubt be found to occur in other groups of insects, were local faunas carefully studied in relation to those of the surrounding countries; and they seem to indicate that climate and other physical causes have, in some cases, a very powerful effect in modifying specific form and colour, and thus directly aid in producing the endless variety of nature."



With regard to butterflies of Celebes belonging to different families, they present "a peculiarity of outline which distinguishes them at a glance from those of any other part of the world:"[65] it is that the upper wings {86} are generally more elongated and the anterior margin more curved. Moreover, there is, in most instances, near the base an abrupt bend or elbow, which in some species is very conspicuous. Mr. Wallace endeavours to explain {87} this phenomenon by the supposed presence at some time of special persecutors of the modified forms, supporting the opinion by the remark that small, obscure, very rapidly flying and mimicked kinds have not had the wing modified. Such an enemy occasioning increased powers of flight, or rapidity in turning, he adds, "one would naturally suppose to be an insectivorous bird; but it is a remarkable fact that most of the genera of fly-catchers of Borneo and Java on the one side, and of the Moluccas on the other, are almost entirely absent from Celebes. Their place seems to be supplied by the caterpillar-catchers, of which six or seven species are known from Celebes, and are very numerous in individuals. We have no positive evidence that these birds pursue butterflies on the wing, but it is highly probable that they do so when other food is scarce. Mr. Bates suggested to me that the larger dragon-flies prey upon butterflies, but I did not notice that they were more abundant in Celebes than elsewhere."[66]

Now, every opinion or conjecture of Mr. Wallace is worthy of respectful and attentive consideration, but the explanation suggested and before referred to hardly seems a satisfactory one. What the past fauna of Celebes may have been is as yet conjectural. Mr. Wallace tells us that now there is a remarkable scarcity of fly-catchers, and that their place is supplied by birds of which it can only be said that it is "highly probable" that they chase butterflies "when other food is scarce." The quick eye of Mr. Wallace failed to detect them in the act, as also to note any unusual abundance of other insectivorous forms, which therefore, considering Mr. Wallace's zeal and powers of observation, we may conclude do not exist. Moreover, even if there ever has been an abundance of such, it is by no means certain that they would have succeeded in producing the conformation in question, for the effect of this peculiar curvature on flight is by no means clear. We have here, then, a structure hypothetically explained by an uncertain {88} property induced by a cause the presence of which is only conjectural.

Surely it is not unreasonable to class this instance with the others before given, in which a common modification of form or colour coexists with a certain geographical distribution quite independently of the destructive agencies of animals. If physical causes connected with locality can abbreviate or annihilate the tails of certain butterflies, why may not similar causes produce an elbow-like prominence on the wings of other butterflies? There are many such instances of simultaneous modification. Mr. Darwin himself[67] quotes Mr. Gould as believing that birds of the same species are more brightly coloured under a clear atmosphere, than when living on islands or near the coast. Mr. Darwin also informs us that Wollaston is convinced that residence near the sea affects the colour of insects; and finally, that Moquin-Tandon gives a list of plants which, when growing near the sea-shore, have their leaves in some degree fleshy, though not so elsewhere. In his work on "Animals and Plants under Domestication,"[68] Mr. Darwin refers to M. Costa as having (in Bull. de la Soc. Imp. d'Acclimat. tome viii. p. 351) stated "that young shells taken from the shores of England and placed in the Mediterranean at once altered their manner of growth, and formed prominent diverging rays like those on the shells of the proper Mediterranean oyster;" also to Mr. Meehan, as stating (Proc. Acad. Nat. Sc. of Philadelphia, Jan. 28, 1862) "that twenty-nine kinds of American trees all differ from their nearest European allies in a similar manner, leaves less toothed, buds and seeds smaller, fewer branchlets," &c. These are striking examples indeed!

But cases of simultaneous and similar modifications abound on all sides. Even as regards our own species there is a very generally admitted opinion that a new type has been developed in the United States, and this in about a couple of centuries only, and in a vast multitude of individuals of {89} diverse ancestry. The instances here given, however, must suffice, though more could easily be added.



It may be well now to turn to groups presenting similar variations, not through, but independently of, geographical distribution, and, as far as we know, independently of conditions other than some peculiar nature and tendency (as yet unexplained) common to members of such groups, which nature and tendency seem to induce them to vary in certain definite lines or directions which are different in different groups. Thus with regard to the group of insects, of which the walking leaf is a member, Mr. Wallace observes:[69] "The whole family[70] of the Phasmidae, or spectres, to which this insect belongs, is more or less imitative, and a great number of the species are called 'walking-stick insects,' from their singular {90} resemblance to twigs and branches."



Again, Mr. Wallace[71] tells us of no less than four kinds of orioles, which birds mimic, more or less, four species of a genus of honey-suckers, the weak orioles finding their profit in being mistaken by certain birds of prey for the strong, active, and gregarious honey-suckers. Now, many other birds would be benefited by similar mimicry, which is none the less confined, in this part of the world, to the oriole genus. It is true that the absence of mimicry in other forms may be explained by their possessing some other (as yet unobserved) means of preservation. But it is nevertheless remarkable, not so much that one species should mimic, as that no less than four should do so in different ways and degrees, all these{91} four belonging to one and the same genus.



In other cases, however, there is not even the help of protective action to account for the phenomenon. Thus we have the wonderful birds of Paradise,[72] which agree in developing plumage unequalled in beauty, but a beauty which, as to details, is of different kinds, and produced in different ways in different species. To develop "beauty and singularity of plumage" is a character of the group, but not of any one definite kind, to be explained merely by inheritance.

{92}

Again, we have the very curious horned flies,[73] which agree indeed in a common peculiarity, but in one singularly different in detail, in different species and not known to have any protecting effect.

Amongst plants, also, we meet with the same peculiarity. The great group of Orchids presents a number of species which offer strange and bizarre {93} approximations to different animal forms, and which have often the appearance of cases of mimicry, as it were in an incipient stage.



The number of similar instances which could be brought forward from amongst animals and plants is very great, but the examples given are, it is {94} hoped, amply sufficient to point towards the conclusion which other facts will, it is thought, establish, viz. that there are causes operating (in the evocation of these harmonious diverging resemblances) other than "Natural Selection," or heredity, and other even than merely geographical, climatal, or any simply external conditions.

Many cases have been adduced of striking likenesses between different animals, not due to inheritance; but this should be the less surprising, in that the very same individual presents us with likenesses between different parts of its body (e.g., between the several joints of the backbone), which are certainly not so explicable. This, however, leads to a rather large subject, which will be spoken of in the eighth chapter of the present work. Here it will be enough to affirm (leaving the proof of the assertion till later) that parts are often homologous which have no direct genetic relationship,—a fact which harmonizes well with the other facts here given, but which "Natural Selection," pure and simple, seems unable to explain.

But surely the independent appearance of similar organic forms is what we might expect, a priori, from the independent appearance of similar inorganic ones. As Mr. G. H. Lewes well observes,[74] "We do not suppose the carbonates and phosphates found in various parts of the globe—we do not suppose that the families of alkaloids and salts have any nearer kinship than that which consists in the similarity of their elements, and the conditions of their combination. Hence, in organisms, as in salts, morphological identity may be due to a community of causal connexion, rather than community of descent.

"Mr. Darwin justly holds it to be incredible that individuals identically the same should have been produced through Natural Selection from parents specifically distinct, but he will not deny that identical forms may issue from parents genetically distinct, when these parent forms and {95} the conditions of production are identical. To deny this would be to deny the law of causation."

Professor Huxley has, however, suggested[75] that such mineral identity may be explained by applying also to minerals a law of descent; that is, by considering such similar forms as the descendants of atoms which inhabited one special part of the primitive nebular cosmos, each considerable space of which may be supposed to have been under the influence of somewhat different conditions.

Surely, however, there can be no real parity between the relationship of existing minerals to nebular atoms, and the relationship of existing animals and plants to the earliest organisms. In the first place, the latter have produced others by generative multiplication, which mineral atoms never did. In the second, existing animals and plants spring from the living tissues of preceding animals and plants, while existing minerals spring from the chemical affinity of separate elements. Carbonate of soda is not formed, by a process of reproduction, from other carbonate of soda, but directly by the suitable juxtaposition of carbon, oxygen, and sodium.

Instead of approximating animals and minerals in the mode suggested, it may be that they are to be approximated in quite a contrary fashion; namely, by attributing to mineral species an internal innate power. For, as we must attribute to each elementary atom an innate power and tendency to form (under the requisite external conditions) certain unions with other atoms, so we may attribute to certain mineral species—as crystals—an innate power and tendency to exhibit (the proper conditions being supplied) a definite and symmetrical external form. The distinction between animals and vegetables on the one hand, and minerals on the other, is that, while in the organic world close similarity is the result sometimes of inheritance, sometimes of direct production independently of parental action, in the{96} inorganic world the latter is the constant and only mode in which such similarity is produced.

When we come to consider the relations of species to space—in other words, the geographical distribution of organisms—it will be necessary to return somewhat to the subject of the independent origin of closely similar forms, in regard to which some additional remarks will be found towards the end of the seventh chapter.

In this third chapter an effort has been made to show that while on the Darwinian theory concordant variations are extremely improbable, yet Nature presents us with abundant examples of such; the most striking of which are, perhaps, the higher organs of sense. Also that an important influence is exercised by conditions connected with geographical distribution, but that a deeper-seated influence is at work, which is hinted at by those special tendencies in definite directions, which are the properties of certain groups. Finally, that these facts, when taken together, afford strong evidence that "Natural Selection" has not been the exclusive or predominant cause of the various organic structural peculiarities. This conclusion has also been re-enforced by the consideration of phenomena presented to us by the inorganic world. [Page 97]

* * * * *

CHAPTER IV.

MINUTE AND GRADUAL MODIFICATIONS.

There are difficulties as to minute modifications, even if not fortuitous.—Examples of sudden and considerable modifications of different kinds.—Professor Owen's view.—Mr. Wallace.—Professor Huxley.—Objections to sudden changes.—Labyrinthodont.—Potto.—Cetacea.—As to origin of bird's wing.—Tendrils of climbing plants.—Animals once supposed to be connecting links.—Early specialization of structure.—Macrauchenia.—Glyptodon.—Sabre-toothed tiger.—Conclusion.

Not only are there good reasons against the acceptance of the exclusive operation of "Natural Selection" as the one means of specific origination, but there are difficulties in the way of accounting for such origination by the sole action of modifications which are infinitesimal and minute, whether fortuitous or not.

Arguments may yet be advanced in favour of the view that new species have from time to time manifested themselves with suddenness, and by modifications appearing at once (as great in degree as are those which separate Hipparion from Equus), the species remaining stable in the intervals of such modifications: by stable being meant that their variations only extend for a certain degree in various directions, like oscillations in a stable equilibrium. This is the conception of Mr. Galton,[76] who compares the development of species with a many {98} facetted spheroid tumbling over from one facet, or stable equilibrium, to another. The existence of internal conditions in animals corresponding with such facets is denied by pure Darwinians, but it is contended in this work, though not in this chapter, that something may also be said for their existence.

The considerations brought forward in the last two chapters, namely, the difficulties with regard to incipient and closely similar structures respectively, together with palaeontological considerations to be noticed later, appear to point strongly in the direction of sudden and considerable changes. This is notably the case as regards the young oysters already mentioned, which were taken from the shores of England and placed in the Mediterranean, and at once altered their mode of growth and formed prominent diverging rays, like those of the proper Mediterranean oyster; as also the twenty-nine kinds of American trees, all differing from their nearest European allies similarly—"leaves less toothed, buds and seeds smaller, fewer branchlets," &c. To these may be added other facts given by Mr. Darwin. Thus he says, "that climate, to a certain extent, directly modifies the form of dogs."[77]

The Rev. R. Everett found that setters at Delhi, though most carefully paired, yet had young with "nostrils more contracted, noses more pointed, size inferior, and limbs more slender." Again, cats at Mombas, on the coast of Africa, have short stiff hairs instead of fur, and a cat at Algoa Bay, when left only eight weeks at Mombas, "underwent a complete metamorphosis, having parted with its sandy-coloured fur."[78] The conditions of life seem to produce a considerable effect on horses, and instances are given by Mr. Darwin of pony breeds[79] having independently arisen in different parts of the world, possessing a certain similarity in their physical {99} conditions. Also changes due to climate may be brought about at once in a second generation, though no appreciable modification is shown by the first. Thus "Sir Charles Lyell mentions that some Englishmen, engaged in conducting the operations of the Real del Monte Company in Mexico, carried out with them some greyhounds of the best breed to hunt the hares which abound in that country. It was found that the greyhounds could not support the fatigues of a long chase in this attenuated atmosphere, and before they could come up with their prey they lay down gasping for breath; but these same animals have produced whelps, which have grown up, and are not in the least degree incommoded by the want of density in the air, but run down the hares with as much ease as do the fleetest of their race in this country."[80]

We have here no action of "Natural Selection;" it was not that certain puppies happened accidentally to be capable of enduring more rarefied air, and so survived, but the offspring were directly modified by the action of surrounding conditions. Neither was the change elaborated by minute modifications in many successive generations, but appeared at once in the second.

With regard once more to sudden alterations of form, Nathusius is said to state positively as to pigs,[81] that the result of common experience and of his experiments was that rich and abundant food, given during youth, tends by some direct action to make the head broader and shorter. Curious jaw appendages often characterize Normandy pigs, according to M. Eudes Deslongchamps. Richardson figures these appendages on the old "Irish greyhound pig," and they are said by Nathusius to appear occasionally in all the long-eared races. Mr. Darwin observes,[82] "As no wild pigs are known to have analogous appendages, we have at present no reason to {100} suppose that their appearance is due to reversion; and if this be so, we are forced to admit that somewhat complex, though apparently useless structures may be suddenly developed without the aid of selection." Again, "Climate directly affects the thickness of the skin and hair" of cattle.[83] In the English climate an individual Porto Santo rabbit[84] recovered the proper colour of its fur in rather less than four years. The effect of the climate of India on the turkey is considerable. Mr. Blyth[85] describes it as being much degenerated in size, "utterly incapable of rising on the wing," of a black colour, and "with long pendulous appendages over the beak enormously developed." Mr. Darwin again tells us that there has suddenly appeared in a bed of common broccoli a peculiar variety, faithfully transmitting its newly acquired and remarkable characters;[86] also that there have been a rapid transformation and transplantation of American varieties of maize with a European variety;[87] that certainly "the Ancon and Manchamp breeds of sheep," and that (all but certainly) Niata cattle, turnspit and pug dogs, jumper and frizzled fowls, short-faced tumbler pigeons, hook-billed ducks, &c., and a multitude of vegetable varieties, have suddenly appeared in nearly the same state as we now see them.[88] Lastly, Mr. Darwin tells us, that there has been an occasional development (in five distinct cases) in England of the "japanned" or "black-shouldered peacock" (Pavo nigripennis), a distinct species, according to Dr. Sclater,[89] yet arising in Sir J. Trevelyan's flock composed entirely of the common kind, and increasing, "to the extinction of the previously existing breed."[90] Mr. Darwin's only explanation of the phenomena (on the supposition of the species being distinct) is by{101} reversion, owing to a supposed ancestral cross. But he candidly admits, "I have heard of no other such case in the animal or vegetable kingdom." On the supposition of its being only a variety, he observes, "The case is the most remarkable ever recorded of the abrupt appearance of a new form, which so closely resembles a true species, that it has deceived one of the most experienced of living ornithologists."

As to plants, M. C. Naudin[91] has given the following instances of the sudden origination of apparently permanent forms. "The first case mentioned is that of a poppy, which took on a remarkable variation in its fruit—a crown of secondary capsules being added to the normal central capsule. A field of such poppies was grown, and M. Goeppert, with seed from this field, obtained still this monstrous form in great quantity. Deformities of ferns are sometimes sought after by fern-growers. They are now always obtained by taking spores from the abnormal parts of the monstrous fern; from which spores ferns presenting the same peculiarities invariably grow.... The most remarkable case is that observed by Dr. Godron, of Nancy. In 1861 that botanist observed, amongst a sowing of Datura tatula, the fruits of which are very spinous, a single individual of which the capsule was perfectly smooth. The seeds taken from this plant all furnished plants having the character of this individual. The fifth and sixth generations are now growing without exhibiting the least tendency to revert to the spinous form. More remarkable still, when crossed with the normal Datura tatula, hybrids were produced, which, in the second generation, reverted to the original types, as true hybrids do."

There are, then, abundant instances to prove that considerable {102} modifications may suddenly develop themselves, either due to external conditions or to obscure internal causes in the organisms which exhibit them. Moreover, these modifications, from whatever cause arising, are capable of reproduction—the modified individuals "breeding true."

The question is whether new species have been developed by non-fortuitous variations which are insignificant and minute, or whether such variations have been comparatively sudden, and of appreciable size and importance? Either hypothesis will suit the views here maintained equally well (those views being opposed only to fortuitous, indefinite variations), but the latter is the more remote from the Darwinian conception, and yet has much to be said in its favour.

Professor Owen considers, with regard to specific origination, that natural history "teaches that the change would be sudden and considerable: it opposes the idea that species are transmitted by minute and slow degrees."[92] "An innate tendency to deviate from parental type, operating through periods of adequate duration," being "the most probable nature, or way of operation of the secondary law, whereby species have been derived one from the other."[93]

Now, considering the number of instances adduced of sudden modifications in domestic animals, it is somewhat startling to meet with Mr. Darwin's dogmatic assertion that it is "a false belief" that natural species have often originated in the same abrupt manner. The belief may be false, but it is difficult to see how its falsehood can be positively asserted.

It is demonstrated by Mr. Darwin's careful weighings and measurements, that, though little used parts in domestic animals get reduced in weight and somewhat in size, yet that they show no inclination to become truly "rudimentary structures." Accordingly he asserts[94] that such {103} rudimentary parts are formed "suddenly, by arrest of development" in domesticated animals, but in wild animals slowly. The latter assertion, however, is a mere assertion; necessary, perhaps, for the theory of "Natural Selection," but as yet unproved by facts.

But why should not these changes take place suddenly in a state of nature? As Mr. Murphy says,[95] "It may be true that we have no evidence of the origin of wild species in this way. But this is not a case in which negative evidence proves anything. We have never witnessed the origin of a wild species by any process whatever; and if a species were to come suddenly into being in the wild state, as the Ancon Sheep did under domestication, how could you ascertain the fact? If the first of a newly-begotten species were found, the fact of its discovery would tell nothing about its origin. Naturalists would register it as a very rare species, having been only once met with, but they would have no means of knowing whether it were the first or the last of its race."

To this Mr. Wallace has replied (in his review of Mr. Murphy's work in Nature[96]), by objecting that sudden changes could very rarely be useful, because each kind of animal is a nicely balanced and adjusted whole, any one sudden modification of which would in most cases be hurtful unless accompanied by other simultaneous and harmonious modifications. If, however, it is not unlikely that there is an innate tendency to deviate at certain times, and under certain conditions, it is no more unlikely that that innate tendency should be an harmonious one, calculated to simultaneously adjust the various parts of the organism to their new relations. The objection as to the sudden abortion of rudimentary organs may be similarly met.

Professor Huxley seems now disposed to accept the, at least {104} occasional, intervention of sudden and considerable variations. In his review of Professor Koelliker's[97] criticisms, he himself says,[98] "We greatly suspect that she" (i.e. Nature) "does make considerable jumps in the way of variation now and then, and that these saltations give rise to some of the gaps which appear to exist in the series of known forms."