Genesis of Species
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.
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 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!
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.
Now, if we were to concede that the ascidians were the common ancestors 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 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, 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. 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: “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: “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 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:” it is that the upper wings 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 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.”