The Evolution of Man, V.2, Ernst Haeckel [free ebook reader for pc txt] 📗

formed from the root-sheaths of the disappearing wool-fibres. The embryonic wool-coat usually, in the case of the human embryo, covers the whole body, with the exception of the palms of the hands and soles of the feet. These parts are always bare, as in the case of apes and of most other mammals. Sometimes the wool-coat of the embryo has a striking effect, by its colour, on the later permanent hair-coat. Hence it happens occasionally, for instance, among our Indo-Germanic races, that children of blond parents seem--to the dismay of the latter--to be covered at birth with a dark brown or even a black woolly coat. Not until this has disappeared do we see the permanent blond hair which the child has inherited. Sometimes the darker coat remains for weeks, and even months, after birth. This remarkable woolly coat of the human embryo is a legacy from the apes, our ancient long-haired ancestors.

(FIGURE 2.288. Mammary gland of a new-born infant, a original central gland, b small and c large buds of same. (From Langer.))

It is not less noteworthy that many of the higher apes approach man in the thinness of the hair on various parts of the body. With most of the apes, especially the higher Catarrhines (or narrow-nosed apes), the face is mostly, or entirely, bare, or at least it has hair no longer or thicker than that of man. In their case, too, the back of the head is usually provided with a thicker growth of hair; this is lacking, however, in the case of the bald-headed chimpanzee (Anthropithecus calvus). The males of many species of apes have a considerable beard on the cheeks and chin; this sign of the masculine sex has been acquired by sexual selection. Many species of apes have a very thin covering of hair on the breast and the upper side of the limbs--much thinner than on the back or the under side of the limbs. On the other hand, we are often astonished to find tufts of hair on the shoulders, back, and extremities of members of our Indo-Germanic and of the Semitic races. Exceptional hair on the face, as on the whole body, is hereditary in certain families of hairy men. The quantity and the quality of the hair on head and chin are also conspicuously transmitted in families. These extraordinary variations in the total and partial hairy coat of the body, which are so noticeable, not only in comparing different races of men, but also in comparing different families of the same race, can only be explained on the assumption that in man the hairy coat is, on the whole, a rudimentary organ, a useless inheritance from the more thickly-coated apes. In this man resembles the elephant, rhinoceros, hippopotamus, whale, and other mammals of various orders, which have also, almost entirely or for the most part, lost their hairy coats by adaptation.

(FIGURE 2.289. Embryo of a bear (Ursus arctos), twice natural size. A seen from ventral side, B from the left.)

The particular process of adaptation by which man lost the growth of hair on most parts of his body, and retained or augmented it at some points, was most probably sexual selection. As Darwin luminously showed in his Descent of Man, sexual selection has been very active in this respect. As the male anthropoid apes chose the females with the least hair, and the females favoured the males with the finest growths on chin and head, the general coating of the body gradually degenerated, and the hair of the beard and head was more strongly developed. The growth of hair at other parts of the body (arm-pit, pubic region) was also probably due to sexual selection. Moreover, changes of climate, or habits, and other adaptations unknown to us, may have assisted the disappearance of the hairy coat.

The fact that our coat of hair is inherited directly from the anthropoid apes is proved in an interesting way, according to Darwin, by the direction of the rudimentary hairs on our arms, which cannot be explained in any other way. Both on the upper and the lower part of the arm they point towards the elbow. Here they meet at an obtuse angle. This curious arrangement is found only in the anthropoid apes--gorilla, chimpanzee, orang, and several species of gibbons--besides man (Figures 1.203 and 1.207). In other species of gibbon the hairs are pointed towards the hand both in the upper and lower arm, as in the rest of the mammals. We can easily explain this remarkable peculiarity of the anthropoids and man on the theory that our common ancestors were accustomed (as the anthropoid apes are to-day) to place their hands over their heads, or across a branch above their heads, during rain. In this position, the fact that the hairs point downwards helps the rain to run off. Thus the direction of the hair on the lower part of our arm reminds us to-day of that useful custom of our anthropoid ancestors.

The nervous system in man and all the other Vertebrates is, when fully formed, an extremely complex apparatus, that we may compare, in anatomic structure and physiological function, with an extensive telegraphic system. The chief station of the system is the central marrow or central nervous system, the innumerable ganglionic cells or neurona (Figure 1.9) of which are connected by branching processes with each other and with numbers of very fine conducting wires. The latter are the peripheral and ubiquitous nerve-fibres; with their terminal apparatus, the sense-organs, etc., they constitute the conducting marrow or peripheral nervous system. Some of them--the sensory nerve-fibres--conduct the impressions from the skin and other sense-organs to the central marrow; others--the motor nerve-fibres--convey the commands of the will to the muscles.

The central nervous system or central marrow (medulla centralis) is the real organ of psychic action in the narrower sense. However we conceive the intimate connection of this organ and its functions, it is certain that its characteristic actions, which we call sensation, will, and thought, are inseparably dependent on the normal development of the material organ in man and all the higher animals. We must, therefore, pay particular attention to the evolution of the latter. As it can give us most important information regarding the nature of the "soul," it should be full of interest. If the central marrow develops in just the same way in the human embryo as in the embryo of the other mammals, the evolution of the human psychic organ from the central organ of the other mammals, and through them from the lower vertebrates, must be beyond question. No one can doubt the momentous bearing of these embryonic phenomena.

(FIGURE 2.290. Human embryo, three months old, natural size, from the dorsal side: brain and spinal cord exposed. (From Kolliker.) h cerebral hemispheres (fore brain), m corpora quadrigemina (middle brain), c cerebellum (hind brain): under the latter is the triangular medulla oblongata (after brain).

FIGURE 2.291. Central marrow of a human embryo, four months old, natural size, from the back. (From Kolliker.) h large hemispheres, v quadrigemina, c cerebellum, mo medulla oblongata: underneath it the spinal cord.)

In order to understand them fully we must first say a word or two of the general form and the anatomic composition of the mature human central marrow. Like the central nervous system of all the other Craniotes, it consists of two parts, the head-marrow or brain (medulla capitis or encephalon) and the spinal-marrow (medulla spinalis or notomyelon). The one is enclosed in the bony skull, the other in the bony vertebral column. Twelve pairs of cerebral nerves proceed from the brain, and thirty-one pairs of spinal nerves from the spinal cord, to the rest of the body (Figure 1.171). On general anatomic investigation the spinal marrow is found to be a cylindrical cord, with a spindle-shaped bulb both in the region of the neck above (at the last cervical vertebra) and the region of the loins (at the first lumbar vertebra) below (Figure 2.291). At the cervical bulb the strong nerves of the upper limbs, and at the lumbar bulb those of the lower limbs, proceed from the spinal cord. Above, the latter passes into the brain through the medulla oblongata (Figure 2.291 mo). The spinal cord seems to be a thick mass of nervous matter, but it has a narrow canal at its axis, which passes into the further cerebral ventricles above, and is filled, like these, with a clear fluid.

The brain is a large nerve-mass, occupying the greater part of the skull, of most elaborate structure. On general examination it divides into two parts, the cerebrum and cerebellum. The cerebrum lies in front and above, and has the familiar characteristic convolutions and furrows on its surface (Figures 2.292 and 2.293). On the upper side it is divided by a deep longitudinal fissure into two halves, the cerebral hemispheres; these are connected by the corpus callosum. The large cerebrum is separated from the small cerebellum by a deep transverse furrow. The latter lies behind and below, and has also numbers of furrows, but much finer and more regular, with convolutions between, at its surface. The cerebellum also is divided by a longitudinal fissure into two halves, the "small hemispheres"; these are connected by a worm-shaped piece, the vermis cerebelli, above, and by the broad pons Varolii below (Figure 2.292 VI).

(FIGURE 2.292. The human brain, seen from below. (From H. Meyer.) Above (in front) is the cerebrum with its extensive branching furrows; below (behind) the cerebellum with its narrow parallel furrows. The Roman numbers I to XII indicate the roots of the twelve pairs of cerebral nerves in a series towards the rear.)

But comparative anatomy and ontogeny teach us that in man and all the other Craniotes the brain is at first composed, not of these two, but of three, and afterwards five, consecutive parts. These are found in just the same form--as five consecutive vesicles--in the embryo of all the Craniotes, from the Cyclostoma and fishes to man. But, however much they agree in their rudimentary condition, they differ considerably afterwards. In man and the higher mammals the first of these ventricles, the cerebrum, grows so much that in its mature condition it is by far the largest and heaviest part of the brain. To it belong not only the large hemispheres, but also the corpus callosum that unites them, the olfactory lobes, from which the olfactory nerves start, and most of the structures that are found at the roof and bottom of the large lateral ventricles inside the two hemispheres, such as the corpora striata. On the other hand, the optic thalami, which lie between the latter, belong to the second division, which develops from the "intermediate brain "; to the same section belong the single third cerebral ventricle and the structures that are known as the corpora geniculata, the infundibulum, and the pineal gland. Behind these parts we find, between the cerebrum and cerebellum, a small ganglion composed of two prominences, which is called the corpus quadrigeminum on account of a superficial transverse fissure cutting across (Figures 2.290 m and 2.291 v). Although this quadrigeminum is very insignificant in man and the higher mammals, it forms a special third section, greatly developed in the lower vertebrates, the "middle brain." The fourth section is the "hind-brain" or little brain (cerebellum) in the narrower sense, with the single median part, the vermis, and the pair of lateral parts, the "small hemispheres" (Figure 2.291 c). Finally, we have the fifth and last section, the medulla oblongata (Figure 2.291 mo), which contains the single fourth cerebral cavity and the contiguous parts (pyramids, olivary bodies, corpora restiformia). The medulla oblongata passes straight into the medulla spinalis (spinal cord). The narrow central canal of the spinal cord continues above into the quadrangular fourth cerebral cavity of the medulla oblongata, the floor of which is the quadrangular depression. From here a narrow duct, called "the aqueduct of Sylvius," passes through the corpus quadrigeminum to the third cerebral ventricle, which lies