something of this kind: if the evolution theory is true, then it in conceivable that the reason why the embryo of a bird passes through a stage in which its pharynx presents some resemblance to that of a fish is that a remote ancestor of the bird possessed a pharynx with lateral apertures such as are at present found in fishes.
But the explanation is sometimes pushed even further, and it is said that these pharyngeal apertures of the ancestral bird had the same respiratory function as the corresponding structures in modern fishes. That this is going too far a little reflection will show. For if it be admitted that all so-called vestigial structures had once the same function as the homologous structures when fully developed in other animals, it becomes necessary to admit that male mammals must once have had fully developed mammary glands and suckled the young, that female mammals formerly were provided with a functional penis, and that in species in which the females have a trace of the secondary sexual characters of the male the latter were once common to both sexes. The second and more extended form of the explanation plainly introduces a considerable amount of contentious matter, and it will be advisable, in the first instance, at any rate, to confine ourselves to a critical examination of the less ambitious conception. This explanation obviously implies the view that in the course of evolution the tendency has been for structures to persist in the embryo after they have been lost in the adult. Is there any justification for this view? It is clearly impossible to get any direct evidence, because, as explained above, we have no knowledge of the ancestors of living animals; but if we assume the evolution theory to be true, there is a certain amount of indirect evidence which is distinctly opposed to the view. As is well known, living birds are without teeth, but it is generally assumed that their edentulous condition has been comparatively recently acquired, and that they are descended from animals which, at a time not very remote from the present, possessed teeth. Considering the resemblance of birds to other terrestrial vertebrates, and the fact that extinct birds, not greatly differing from birds now living, are known to have had teeth, it must be allowed that there is some warrant for the assumption. Yet in no single case has it been certainly shown that any trace of teeth has been developed in the embryo. The same remark applies to a large number of similar cases; for instance, the reduced digits of the bird’s hand and foot and the limbs of snakes. Moreover, organs which are supposed to have become recently reduced and functionless in the adult are also reduced in the embryo; for instance, digits 3 and 4 of the horse’s foot, the hind limbs of whales (G. A. Guldberg and F. Nansen, “On the Development and Structure of Whales,” Bergen Museum, 1894), the spiracle of Elasmobranchii. In fact, considerations of this kind distinctly point to the view that any tendency to the reduction or enlargement of an organ in the adult is shared approximately to the same extent by the embryo. But there are undoubtedly some, though not many, cases in which organs which were presumably present in an ancestral adult have persisted in the embryo of the modern form. As an instance may be mentioned the presence in whale-bone whales of imperfectly formed teeth, which are absorbed comparatively early in foetal life (Julin, Arch. biologie, i., 1880, p. 75).
It therefore becomes necessary to inquire why in some cases an organ is retained by the embryo after its loss by the adult, whereas in other cases it dwindles and presumably disappears simultaneously in the embryo and the adult. The whole question is examined and discussed by the present writer in the Quarterly Journal of Microscopical Science, xxxvi., 1894, p. 35, and the conclusions there reached are as follows:—A disappearing adult organ is not retained in a relatively greater development by an organism in the earlier stages of its individual growth unless it is of functional importance to the young form. In cases in which the whole development is embryonic this rarely happens, because the conditions of embryonic life are so different from free life that functional embryonic organs are usually organs sui generis, e.g. the placenta, amnion, &c., which cannot be traced to a modification of organs previously present in the adult. It does, however, appear to have happened sometimes, and as an instance of it may be mentioned the ductus arteriosus of the Sauropsidan and Mammalian embryo. On the other hand, when there is a considerable period of larval life, it does appear that there is a strong case for thinking that organs which have been lost by the adult may be retained and made use of by the larva. The best-known example that can be given of this is the tadpole of the frog. Here we find organs, viz. gills and gill-slits, which are universally regarded as having been attributes of all terrestrial Vertebrata in an earlier and aquatic condition, and we also notice that their retention is due to their being useful on account of the supposed ancient conditions of life having been retained. Many other instances, more or less plausible, of a like retention of ancestral features by larvae might be mentioned, and it must be conceded that there are strong reasons for supposing that larvae often retain traces, more or less complete, of ancestral stages of structure. But this admission does not carry with it any obligation to accept the widely prevalent view that larval history can in any way be regarded as a recapitulation of ancestral history. Far from it, for larvae in retaining some ancestral features are in no way different from adults; they only differ from adults in the features which they have retained. Both larvae and adults retain ancestral features, and both have been modified by an adaptation to their respective conditions of life which has ever been becoming more perfect.
The conclusion, then, has been reached, that whereas larvae frequently retain traces of ancestral stages of adult structure, embryos will rarely do so; and we are confronted again with the question, How are we to account for the presence in the embryo of numerous functionless organs which cannot be explained otherwise than as having been inherited from a previous condition in which they were functional? The answer is that the only organs of this kind which have been retained are organs which have been retained by the larvae of the ancestors after they have been lost by the adult, and have become in this way impressed upon the development. As an illustration taken from current natural history of the manner in which larval characters are in actual process of becoming embryonic may be mentioned the case of the viviparous salamander (Salamander atra), in which the gills, &c., are all developed but never used, the animal being born without them. In other and closely allied species of salamander there is a considerable period of larval life in which the gills and gill-slits are functional, but in this species the larval stage, for the existence of which there was a distinct reason, viz. the entirely aquatic habits of life in the young state, has become at one stroke embryonic by its simple absorption into the embryonic period. The view, then, that embryonic development is essentially a recapitulation of ancestral history must be given up; it contains only a few references to ancestral history, namely, those which have been preserved probably in a much modified form by previous larvae.
We must now pass to the consideration of another supposed law of embryology—the so-called law of v. Baer. This generalization is usually stated as follows:—Embryos of different species of the same group are more alike than adults, and the resemblances are greater the younger Law of v. Baer. the embryo examined. Great importance has been attached to this generalization by embryologists and naturalists, and it is very widely accepted. Nevertheless, it is open to serious criticism. If it were true, we should expect to find that embryos of closely similar species would be indistinguishable, but this is notoriously not the case. On the contrary, they often differ more than do the adults, in support of which statement the embryos of the different species of Peripatus may be referred to. The generalization undoubtedly had its origin in the fact that there is what may be called a family resemblance between embryos, but this resemblance, which is by no means exact, is purely superficial, and does not extend to anatomical detail. On the contrary, it may be fairly argued that in some cases embryos of widely dissimilar members of the same group present anatomical differences of a higher morphological value than do the adults (see Sedgwick, loc. cit.), and, as stated above the
