The Evolution of Man, vol 2 by Ernst Haeckel (the top 100 crime novels of all time TXT) 📖

is of no use whatever to us, and is only interesting as the last relic of the nictitating membrane, the third, inner eye-lid that had a distinct physiological purpose in the ancient sharks, and still has in many of the Amniotes.

The motor apparatus, in both the skeleton and muscular systems, provides a number of interesting dysteleological arguments. I need only recall the projecting tail of the human embryo, with its rudimentary caudal vertebrae and muscles; this is totally useless in man, but very interesting as the degenerate relic of the long tail of our simian ancestors. From these we have also inherited various bony processes and muscles, which were very useful to them in climbing trees, but are useless to us. At various points of the skin we have cutaneous muscles which we never use—remnants of a strongly-developed cutaneous muscle in our lower mammal ancestors. This “panniculus carnosus” had the function of contracting and creasing the skin to chase away the flies, as we see every day in the horse. Another relic in us of this large cutaneous muscle is the frontal muscle, by which we knit our forehead and raise our eye-brows; but there is another considerable relic of it, the large cutaneous muscle in the neck (platysma myoides), over which we have no voluntary control.

Not only in the systems of animal organs, but also in the vegetal apparatus, we find a number of rudimentary organs, many of which we have already noticed. In the alimentary apparatus there are the thymus-gland and the thyroid gland, the seat of goitre and the relic of a ciliated groove that the Tunicates and Acrania still have in the gill-pannier; there is also the vermiform appendix to the caecum. In the vascular system we have a number of useless cords which represent relics of atrophied vessels that were once active as blood-canals—the ductus Botalli between the pulmonary artery and the aorta, the ductus venosus Arantii between the portal vein and the vena cava, and many others. The many rudimentary organs in the urinary and sexual apparatus are particularly interesting. These are generally developed in one sex and rudimentary in the other. Thus the spermaducts are formed from the Wolffian ducts in the male, whereas in the female we have merely rudimentary traces of them in Gaertner’s canals. On the other hand, in the female the oviducts and womb are developed from the Mullerian ducts, while in the male only the lowest ends of them remain as the “male womb” (vesicula prostatica). Again, the male has in his nipples and mammary glands the rudiments of organs that are usually active only in the female.

A careful anatomic study of the human frame would disclose to us numbers of other rudimentary organs, and these can only be explained on the theory of evolution. Robert Wiedersheim has collected a large number of them in his work on The Human Frame as a Witness to its Past. They are some of the weightiest proofs of the truth of the mechanical conception and the strongest disproofs of the teleological view. If, as the latter demands, man or any other organism had been designed and fitted for his life-purposes from the start and brought into being by a creative act, the existence of these rudimentary organs would be an insoluble enigma; it would be impossible to understand why the Creator had put this useless burden on his creatures to walk a path that is in itself by no means easy. But the theory of evolution gives the simplest possible explanation of them. It says: The rudimentary organs are parts of the body that have fallen into disuse in the course of centuries; they had definite functions in our animal ancestors, but have lost their physiological significance. On account of fresh adaptations they have become superfluous, but are transmitted from generation to generation by heredity, and gradually atrophy.

We have inherited not only these rudimentary parts, but all the organs of our body, from the mammals—proximately from the apes. The human body does not contain a single organ that has not been inherited from the apes. In fact, with the aid of our biogenetic law we can trace the origin of our various systems of organs much further, down to the lowest stages of our ancestry. We can say, for instance, that we have inherited the oldest organs of the body, the external skin and the internal coat of the alimentary system, from the Gastraeads; the nervous and muscular systems from the Platodes; the vascular system, the body-cavity, and the blood from the Vermalia; the chorda and the branchial gut from the Prochordonia; the articulation of the body from the Acrania; the primitive skull and the higher sense-organs from the Cyclostomes; the limbs and jaws from the Selachii; the five-toed foot from the Amphibia; the palate from the Reptiles; the hairy coat, the mammary glands, and the external sexual organs from the Promammals. When we formulated “the law of the ontogenetic connection of systematically related forms,” and determined the relative age of organs, we saw how it was possible to draw phylogenetic conclusions from the ontogenetic succession of systems of organs.

With the aid of this important law and of comparative anatomy we were also enabled to determine “man’s place in nature,” or, as we put it, assign to man his position in the classification of the animal kingdom. In recent zoological classification the animal world is divided into twelve stems or phyla, and these are broadly subdivided into about sixty classes, and these classes into at least 300 orders. In his whole organisation man is most certainly, in the first place, a member of one of these stems, the vertebrate stem; secondly, a member of one particular class in this stem, the Mammals; and thirdly, of one particular order, the order of Primates. He has all the characteristics that distinguish the Vertebrates from the other eleven animal stems, the Mammals from the other sixty classes, and the Primates from the 300 other orders of the animal kingdom. We may turn and twist as we like, but we cannot get over this fact of anatomy and classification. Of late years this fact has given rise to a good deal of discussion, and especially of controversy as to the particular anatomic relationship of man to the apes. The most curious opinions have been advanced on this “ape-question,” or “pithecoid-theory.” It is as well, therefore, to go into it once more and distinguish the essential from the unessential. (Cf. Chapter 2.23.)

We start from the undisputed fact that man is in any case—whether we accept or reject his special blood-relationship to the apes—a true mammal; in fact, a placental mammal. This fundamental fact can be proved so easily at any moment from comparative anatomy that it has been universally admitted since the separation of the Placentals from the lower mammals (Marsupials and Monotremes). But for every consistent subscriber to the theory of evolution it must follow at once that man descends from a common stem-form with all the other Placentals, the stem-ancestor of the Placentals, just as we must admit a common mesozoic ancestor of all the mammals. This is, however, to settle decisively the great and burning question of man’s place in nature, whether or no we go on to admit a nearer or more distant relationship to the apes. Whether man is or is not a member of the ape-order (or, if you prefer, the primate-order.) in the phylogenetic sense, in any case his direct blood-relationship to the rest of the mammals, and especially the Placentals, is established. It is possible that the affinities of the various orders of mammals to each other are different from what we hypothetically assume to-day. But, in any case, the common descent of man and all the other mammals from one stem-form is beyond question. This long-extinct Promammal was probably evolved from Proreptiles during the Triassic period, and must certainly be regarded as the monotreme and oviparous ancestor of ALL the mammals.

If we hold firmly to this fundamental and most important thesis, we shall see the “ape-question” in a very different light from that in which it is usually regarded. Little reflection is then needed to see that it is not nearly so important as it is said to be. The origin of the human race from a series of mammal ancestors, and the historic evolution of these from an earlier series of lower vertebrate ancestors, together with all the weighty conclusions that every thoughtful man deduces therefrom, remain untouched; so far as these are concerned, it is immaterial whether we regard true “apes” as our nearest ancestors or not. But as it has become the fashion to lay the chief stress in the whole question of man’s origin on the “descent from the apes,” I am compelled to return to it once more, and recall the facts of comparative anatomy and ontogeny that give a decisive answer to this “ape-question.”

The shortest way to attain our purpose is that followed by Huxley in 1863 in his able work, which I have already often quoted, Man’s Place in Nature—the way of comparative anatomy and ontogeny. We have to compare impartially all man’s organs with the same organs in the higher apes, and then to examine if the differences between the two are greater than the corresponding differences between the higher and the lower apes. The indubitable and incontestable result of this comparative-anatomical study, conducted with the greatest care and impartiality, was the pithecometra-principle, which we have called the Huxleian law in honour of its formulator—namely, that the differences in organisation between man and the most advanced apes we know are much slighter than the corresponding differences in organisation between the higher and lower apes. We may even give a more precise formula to this law, by excluding the Platyrrhines or American apes as distant relatives, and restricting the comparison to the narrower family-circle of the Catarrhines, the apes of the Old World. Within the limits of this small group of mammals we found the structural differences between the lower and higher catarrhine apes—for instance, the baboon and the gorilla—to be much greater than the differences between the anthropoid apes and man. If we now turn to ontogeny, and find, according to our “law of the ontogenetic connection of systematically related forms,” that the embryos of the anthropoid apes and man retain their resemblance for a longer time than the embryos of the highest and the lowest apes, we are forced, whether we like it or no, to recognise our descent from the order of apes. We can assuredly construct an approximate picture in the imagination of the form of our early Tertiary ancestors from the foregoing facts of comparative anatomy; however we may frame this in detail, it will be the picture of a true ape, and a distinct catarrhine ape. This has been shown so well by Huxley (1863) that the recent attacks of Klaatsch, Virchow, and other anthropologists, have completely failed (cf. Chapter 2.23). All the structural characters that distinguish the Catarrhines from the Platyrrhines are found in man. Hence in the genealogy of the mammals we must derive man immediately from the catarrhine group, and locate the origin of the human race in the Old World. Only the early root-form from which both descended was common to them.

It is, therefore, established beyond question for all impartial scientific inquiry that the human race comes directly from the apes of the Old World; but, at the same time, I repeat that this is not so important in connection with the main question of the origin of man as is commonly supposed. Even if we entirely ignore it, all that we have learned from the zoological facts of comparative anatomy and ontogeny as to the placental character of man remains untouched. These prove beyond all doubt the common descent of man and all the rest of the mammals. Further, the