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

surround the third cerebral ventricle, and the infundibulum and pineal gland. The third vesicle, the middle brain (m), produces the corpora quadrigemina and the aqueduct of Sylvius. From the fourth vesicle, the hind brain (h), develops the greater part of the cerebellum—namely, the vermis and the two small hemispheres. Finally, the fifth vesicle, the after brain (n), forms the medulla oblongata, with the quadrangular pit (the floor of the fourth ventricle), the pyramids, olivary bodies, etc.

We must certainly regard it as a comparative-anatomical and ontogenetic fact of the greatest significance that in all the Craniotes, from the lowest Cyclostomes and fishes up to the apes and man, the brain develops in just the same way in the embryo. The first rudiment of it is always a simple vesicular enlargement of the fore end of the medullary tube. In every case, first three, then five, vesicles develop from this bulb, and the permanent brain with all its complex anatomic structures, of so great a variety in the various classes of Vertebrates, is formed from the five primitive vesicles. When we compare the mature brain of a fish, an amphibian, a reptile, a bird, and a mammal, it seems incredible that we can trace the various parts of these organs, that differ so much internally and externally, to common types. Yet all these different Craniote brains have started with the same rudimentary structure. To convince ourselves of this we have only to compare the corresponding stages of development of the embryos of these different animals.

(FIGURE 2.297. Head of a chick embryo (hatched fifty-eight hours), from the back, magnified forty times. (From Mihalkovics.) vw anterior wall of the fore brain. vh its ventricle. au optic vesicles, mh middle brain, kh hind brain, nh after brain, hz heart (seen from below), vw vitelline veins, us primitive segment, rm spinal cord.)

This comparison is extremely instructive. If we extend it through the whole series of the Craniotes, we soon discover this interesting fact: In the Cyclostomes (the Myxinoida and Petromyzonta), which we have recognised as the lowest and earliest Craniotes, the whole brain remains throughout life at a very low stage, which is very brief and passing in the embryos of the higher Craniotes; they retain the five original sections of the brain unchanged. In the fishes we find an essential and considerable modification of the five vesicles; it is clearly the brain of the Selachii in the first place, and subsequently the brain of the Ganoids, from which the brain of the rest of the fishes on the one hand and of the Dipneusts and Amphibia, and through these of the higher Vertebrates, on the other hand, must be derived. In the fishes and Amphibia (Figure 2.300) there is a preponderant development of the middle brain, and also the after brain, the first, second, and fourth sections remaining very primitive. It is just the reverse in the higher Vertebrates, in which the first and third sections, the cerebrum and cerebellum, are exceptionally developed; while the middle brain and after brain remain small. The corpora quadrigemina are mostly covered by the cerebrum, and the oblongata by the cerebellum. But we find a number of stages of development within the higher Vertebrates themselves. From the Amphibia upwards the brain (and with it the psychic life) develops in two different directions; one of these is followed by the reptiles and birds, and the other by the mammals. The development of the first section, the fore brain, is particularly characteristic of the mammals. It is only in them that the cerebrum becomes so large as to cover all the other parts of the brain (Figures 2.293 and 2.301 to 2.304).

There are also notable variations in the relative position of the cerebral vesicles. In the lower Craniotes they lie originally almost in the same plane. When we examine the brain laterally, we can cut through all five vesicles with a straight line. But in the Amniotes there is a considerable curve in the brain along with the bending of the head and neck; the whole of the upper dorsal surface of the brain develops much more than the under ventral surface. This causes a curve, so that the parts come to lie as follows: The fore brain is right in front and below, the intermediate brain a little higher, and the middle brain highest of all; the hind brain lies a little lower, and the after brain lower still. We find this only in the Amniotes—the reptiles, birds, and mammals.

(FIGURE 2.298. Brain of three craniote embryos in vertical section. A of a shark (Heptarchus), B of a serpent (Coluber), C of a goat (Capra). a fore brain, b intermediate brain, c middle brain, d hind brain, e after brain, s primitive cleft. (From Gegenbaur.)

FIGURE 2.299. Brain of a shark (Scyllium), back view. g fore-brain, h olfactory lobes, which send the large olfactory nerves to the nasal capsule (o), d intermediate brain, b middle brain; behind this the insignificant structure of the hind brain, a after brain. (From Gegenbaur.)

FIGURE 2.300. Brain and spinal cord of the frog. A from the dorsal, B from the ventral side. a olfactory lobes before the (b) fore brain, i infundibulum at the base of the intermediate brain, c middle brain, d hind brain, s quadrangular pit in the after brain, m spinal cord (very short in the frog), m apostrophe roots of the spinal nerves, t terminal fibres of the spinal cord. (From Gegenbaur.)

FIGURE 2.301. Brain of an ox-embryo, two inches in length. (From Mihalkovics, magnified three times.) Left view; the lateral wall of the left hemisphere has been removed, st corpora striata, ml Monro-foramen, ag arterial plexus, ah Ammon’s horn, mh middle brain, kh cerebellum. dv roof of the fourth ventricle, bb pons Varolii, na medulla oblongata.)

Thus, while the brain of the mammals agrees a good deal in general growth with that of the birds and reptiles, there are some striking differences between the two. In the Sauropsids (birds and reptiles) the middle brain and the middle part of the hind brain are well developed. In the mammals these parts do not grow, and the fore-brain develops so much that it overlies the other vesicles. As it continues to grow towards the rear, it at last covers the whole of the rest of the brain, and also encloses the middle parts from the sides (Figures 2.301 to 2.303). This process is of great importance, because the fore brain is the organ of the higher psychic life, and in it those functions of the nerve-cells are discharged which we sum up in the word “soul.” The highest achievements of the animal body—the wonderful manifestations of consciousness and the complex molecular processes of thought—have their seat in the fore brain. We can remove the large hemispheres, piece by piece, from the mammal without killing it, and we then see how the higher functions of consciousness, thought, will, and sensation, are gradually destroyed, and in the end completely extinguished. If the animal is fed artificially, it may be kept alive for a long time, as the destruction of the psychic organs by no means involves the extinction of the faculties of digestion, respiration, circulation, urination—in a word, the vegetative functions. It is only conscious sensation, voluntary movement, thought, and the combination of various higher psychic functions that are affected.

(FIGURE 2.302. Brain of a human embryo, twelve weeks old. (From Mihalkovics, natural size.) Seen from behind and above. ms mantle-furrow, mh corpora quadrigemina (middle brain), vs anterior medullary ala, kh cerebellum, vv fourth ventricle, na medulla oblongata.)

The fore brain, the organ of these functions, only attains this high level of development in the more advanced Placentals, and thus we have the simple explanation of the intellectual superiority of the higher mammals. The soul of most of the lower Placentals is not much above that of the reptiles, but among the higher Placentals we find an uninterrupted gradation of mental power up to the apes and man. In harmony with this we find an astonishing variation in the degree of development of their fore brain, not only qualitatively, but also quantitatively. The mass and weight of the brain are much greater in modern mammals, and the differentiation of its various parts more important, than in their extinct Tertiary ancestors. This can be shown paleontologically in any particular order. The brains of the living ungulates are (relatively to the size of the body) four to six times (in the highest groups even eight times) as large as those of their earlier Tertiary ancestors, the well-preserved skulls of which enable us to determine the size and weight of the brain.

(FIGURE 2.303. Brain of a human embryo, twenty-four weeks old, halved in the median plane: right hemisphere seen from inside. (From Mihalkovics, natural size.) rn olfactory nerve. tr funnel of the intermediate brain, vc anterior commissure, ml Monro-foramen, gw fornix, ds transparent sheath, bl corpus callosum, br fissure at its border, hs occipital fissure, zh cuneus, sf occipital transverse fissure, zb pineal gland, mh corpora quadrigemina, kh cerebellum.

In the lower mammals the surface of the cerebral hemispheres is quite smooth and level, as in the rabbit (Figure 2.304). Moreover, the fore brain remains so small that it does not cover the middle brain. At a stage higher the middle brain is covered, but the hind brain remains free. Finally, in the apes and man, the latter also is covered by the fore brain. We can trace a similar gradual development in the fissures and convolutions that are found on the surface of the cerebrum of the higher mammals (Figures 2.292 and 2.293). If we compare different groups of mammals in regard to these fissures and convolutions, we find that their development proceeds step by step with the advance of mental life.

Of late years great attention has been paid to this special branch of cerebral anatomy, and very striking individual differences have been detected within the limits of the human race. In all human beings of special gifts and high intelligence the convolutions and fissures are much more developed than in the average man; and they are more developed in the latter than in idiots and others of low mental capacity. There is a similar gradation among the mammals in the internal structure of the fore brain. In particular the corpus callosum, that unites the two cerebral hemispheres, is only developed in the Placentals. Other structures—for instance, in the lateral ventricles—that seem at first to be peculiar to man, are also found in the higher apes, and these alone. It was long thought that man had certain distinctive organs in his cerebrum which were not found in any other animal. But careful examination has discovered that this is not the case, but that the characteristic features of the human brain are found in a rudimentary form in the lower apes, and are more or less fully developed in the higher apes. Huxley has convincingly shown, in his Man’s Place in Nature (1863), that the differences in the formation of the brain within the ape-group constitute a deeper gulf between the lower and higher apes than between the higher apes and man.

The comparative anatomy and physiology of the brain of the higher and lower mammals are very instructive, and give important information in connection with the chief questions of psychology.

(FIGURE 2.304. Brain of the rabbit. A from the dorsal, B from the ventral side, lo olfactory lobes, I fore brain, h hypophysis at the base of the intermediate brain, III middle brain, IV hind brain, V after brain, 2 optic nerve, 3 oculo-motor nerve, 5 to 8 cerebral nerves. In A the roof of the right hemisphere (I) is removed, so that we can see the corpora striata in the lateral ventricle. (From Gegenbaur.))

The central marrow (brain and spinal cord) develops from the medullary tube in man just as in all the other mammals, and the