The organ of sight, the eye, is found at the side of the head, also in the shape of a depression (Figures 1.169 l and 1.170 b), to which corresponds a large outgrowth of the foremost cerebral vesicle on each side. Farther behind, at each side of the head, there is a third depression, the first trace of the organ of hearing (Figure 1.169 g).

As yet we can see nothing of the later elaborate structure of these organs, nor of the characteristic build of the face.

(FIGURE 1.174. Development of the lizard's legs (Lacerta agilis), with special relation to their blood-vessels. 1, 3, 5, 7, 9, 11 right fore-leg; 13, 15 left fore-leg; 2, 4, 6, 8, 10, 12 right hind-leg; 14, 16 left hind-leg; SRV lateral veins of the trunk, VU umbilical vein.

(From F. Hochstetter.))

When the human embryo has reached this stage of development, it can still scarcely be distinguished from that of any other higher vertebrate. All the chief parts of the body are now laid down: the head with the primitive skull, the rudiments of the three higher sense-organs and the five cerebral vesicles, and the gill-arches and clefts; the trunk with the spinal cord, the rudiment of the vertebral column, the chain of metamera, the heart and chief blood-vessels, and the kidneys. At this stage man is a higher vertebrate, but shows no essential morphological difference from the embryos of the mammals, the birds, the reptiles, etc. This is an ontogenetic fact of the utmost significance. From it we can gather the most important phylogenetic conclusions.

There is still no trace of the limbs. Although head and trunk are separated and all the princ.i.p.al internal organs are laid down, there is no indication whatever of the "extremities" at this stage; they are formed later on. Here again we have a fact of the utmost interest. It proves that the older vertebrates had no feet, as we find to be the case in the lowest living vertebrates (amphioxus and the cyclostoma).

The descendants of these ancient footless vertebrates only acquired extremities--two fore-legs and two hind-legs--at a much later stage of development. These were at first all alike, though they afterwards vary considerably in structure--becoming fins (of breast and belly) in the fishes, wings and legs in the birds, fore and hind legs in the creeping animals, arms and legs in the apes and man. All these parts develop from the same simple original structure, which forms secondarily from the trunk-wall (Figures 1.172 and 1.173). They have always the appearance of two pairs of small buds, which represent at first simple roundish k.n.o.bs or plates. Gradually each of these plates becomes a large projection, in which we can distinguish a small inner part and a broader outer part. The latter is the rudiment of the foot or hand, the former that of the leg or arm. The similarity of the original rudiment of the limbs in different groups of vertebrates is very striking.

(FIGURE 1.175. Human embryo, five weeks old, half an inch long, seen from the right, magnified ten times. (From Russel Bardeen and Harmon Lewis.) In the undissected head we see the eye, mouth, and ear. In the trunk the skin and part of the muscles have been removed, so that the cartilaginous vertebral column is free; the dorsal root of a spinal nerve goes out from each vertebra (towards the skin of the back). In the middle of the lower half of the figure part of the ribs and intercostal muscles are visible. The skin and muscles have also been removed from the right limbs; the internal rudiments of the five fingers of the hand, and five toes of the foot, are clearly seen within the fin-shaped plate, and also the strong network of nerves that goes from the spinal cord to the extremities. The tail projects under the foot, and to the right of it is the first part of the umbilical cord.)

How the five fingers or toes with their blood-vessels gradually differentiate within the simple fin-like structure of the limbs can be seen in the instance of the lizard in Figure 1.174. They are formed in just the same way in man: in the human embryo of five weeks the five fingers can clearly be distinguished within the fin-plate (Figure 1.175).

The careful study and comparison of human embryos with those of other vertebrates at this stage of development is very instructive, and reveals more mysteries to the impartial student than all the religions in the world put together. For instance, if we compare attentively the three successive stages of development that are represented, in twenty different amniotes we find a remarkable likeness. When we see that as a fact twenty different amniotes of such divergent characters develop from the same embryonic form, we can easily understand that they may all descend from a common ancestor.

(FIGURES 1.176 TO 1.178. Embryos of the bat (Vespertilio murinus) at three different stages. (From Oscar Schultze.) Figure 1.176: Rudimentary limbs (v fore-leg, h hind-leg). l lenticular depression, r olfactory pit, ok upper jaw, uk lower jaw, k2, k3, k4 first, second and third gill-arches, a amnion, n umbilical vessel, d yelk-sac.

Figure 1.177: Rudiment of flying membrane, membranous fold between fore and hind leg. n umbilical vessel, o ear-opening, f flying membrane. Figure 1.178: The flying membrane developed and stretched across the fingers of the hands, which cover the face.)

In the first stage of development, in which the head with the five cerebral vesicles is already clearly indicated, but there are no limbs, the embryos of all the vertebrates, from the fish to man, are only incidentally or not at all different from each other. In the second stage, which shows the limbs, we begin to see differences between the embryos of the lower and higher vertebrates; but the human embryo is still hardly distinguishable from that of the higher mammals. In the third stage, in which the gill-arches have disappeared and the face is formed, the differences become more p.r.o.nounced. These are facts of a significance that cannot be exaggerated.* (* Because they show how the most diverse structures may be developed from a common form. As we actually see this in the case of the embryos, we have a right to a.s.sume it in that of the stem-forms. Nevertheless, this resemblance, however great, is never a real ident.i.ty. Even the embryos of the different individuals of one species are usually not really identical. If the reader can consult the complete edition of this work at a library, he will find six plates ill.u.s.trating these twenty embryos.)

If there is an intimate causal connection between the processes of embryology and stem-history, as we must a.s.sume in virtue of the laws of heredity, several important phylogenetic conclusions follow at once from these ontogenetic facts. The profound and remarkable similarity in the embryonic development of man and the other vertebrates can only be explained when we admit their descent from a common ancestor. As a fact, this common descent is now accepted by all competent scientists; they have subst.i.tuted the natural evolution for the supernatural creation of organisms.

CHAPTER 1.15. FOETAL MEMBRANES AND CIRCULATION.

Among the many interesting phenomena that we have encountered in the course of human embryology, there is an especial importance in the fact that the development of the human body follows from the beginning just the same lines as that of the other viviparous mammals. As a fact, all the embryonic peculiarities that distinguish the mammals from other animals are found also in man; even the ovum with its distinctive membrane (zona pellucida, Figure 1.14) shows the same typical structure in all mammals (apart from the older oviparous monotremes). It has long since been deduced from the structure of the developed man that his natural place in the animal kingdom is among the mammals. Linne (1735) placed him in this cla.s.s with the apes, in one and the same order (primates), in his Systema Naturae. This position is fully confirmed by comparative embryology. We see that man entirely resembles the higher mammals, and most of all the apes, in embryonic development as well as in anatomic structure. And if we seek to understand this ontogenetic agreement in the light of the biogenetic law, we find that it proves clearly and necessarily the descent of man from a series of other mammals, and proximately from the primates. The common origin of man and the other mammals from a single ancient stem-form can no longer be questioned; nor can the immediate blood-relationship of man and the ape.

(FIGURE 1.179. Human embryos from the second to the fifteenth week, natural size, seen from the left, the curved back turned towards the right. (Mostly from Ecker.) II of fourteen days. III of three weeks.

IV of four weeks. V of five weeks. VI of six weeks. VII of seven weeks. VIII of eight weeks. XII of twelve weeks. XV of fifteen weeks.)

The essential agreement in the whole bodily form and inner structure is still visible in the embryo of man and the other mammals at the late stage of development at which the mammal-body can be recognised as such. But at a somewhat earlier stage, in which the limbs, gill-arches, sense-organs, etc., are already outlined, we cannot yet recognise the mammal embryos as such, or distinguish them from those of birds and reptiles. When we consider still earlier stages of development, we are unable to discover any essential difference in bodily structure between the embryos of these higher vertebrates and those of the lower, the amphibia and fishes. If, in fine, we go back to the construction of the body out of the four germinal layers, we are astonished to perceive that these four layers are the same in all vertebrates, and everywhere take a similar part in the building-up of the fundamental organs of the body. If we inquire as to the origin of these four secondary layers, we learn that they always arise in the same way from the two primary layers; and the latter have the same significance in all the metazoa (i.e., all animals except the unicellulars). Finally, we see that the cells which make up the primary germinal layers owe their origin in every case to the repeated cleavage of a single simple cell, the stem-cell or fertilised ovum.

(FIGURE 1.180. Very young human embryo of the fourth week, one-fourth of an inch long (taken from the womb of a suicide eight hours after death). (From Rabl.) n nasal pits, a eye, u lower jaw, z arch of hyoid bone, k3 and k4 third and fourth gill-arch, h heart; s primitive segments, vg fore-limb (arm), hg hind-limb (leg), between the two the ventral pedicle.)

It is impossible to lay too much stress on this remarkable agreement in the chief embryonic features in man and the other animals. We shall make use of it later on for our monophyletic theory of descent--the hypothesis of a common descent of man and all the metazoa from the gastraea. The first rudiments of the princ.i.p.al parts of the body, especially the oldest organ, the alimentary ca.n.a.l, are the same everywhere; they have always the same extremely simple form. All the peculiarities that distinguish the various groups of animals from each other only appear gradually in the course of embryonic development; and the closer the relation of the various groups, the later they are found. We may formulate this phenomenon in a definite law, which may in a sense be regarded as an appendix to our biogenetic law. This is the law of the ontogenetic connection of related animal forms. It runs: The closer the relation of two fully-developed animals in respect of their whole bodily structure, and the nearer they are connected in the cla.s.sification of the animal kingdom, the longer do their embryonic forms retain their ident.i.ty, and the longer is it impossible (or only possible on the ground of subordinate features) to distinguish between their embryos. This law applies to all animals whose embryonic development is, in the main, an hereditary summary of their ancestral history, or in which the original form of development has been faithfully preserved by heredity. When, on the other hand, it has been altered by cenogenesis, or disturbance of development, we find a limitation of the law, which increases in proportion to the introduction of new features by adaptation (cf. Chapter 1.1). Thus the apparent exceptions to the law can always be traced to cenogenesis.

(FIGURE 1.181. Human embryo of the middle of the fifth week, one-third of an inch long. (From Rabl.) Letters as in Figure 1.180, except sk curve of skull, ok upper jaw, hb neck-indentation.)

When we apply to man this law of the ontogenetic connection of related forms, and run rapidly over the earliest stages of human development with an eye to it, we notice first of all the structural ident.i.ty of the ovum in man and the other mammals at the very beginning (Figures 1.1 and 1.14). The human ovum possesses all the distinctive features of the ovum of the viviparous mammals, especially the characteristic formation of its membrane (zona pellucida), which clearly distinguishes it from the ovum of all other animals. When the human foetus has attained the age of fourteen days, it forms a round vesicle (or "embryonic vesicle") about a quarter of an inch in diameter. A thicker part of its border forms a simple sole-shaped embryonic shield one-twelfth of an inch long (Figure 1.133). On its dorsal side we find in the middle line the straight medullary furrow, bordered by the two parallel dorsal or medullary swellings. Behind, it pa.s.ses by the neurenteric ca.n.a.l into the primitive gut or primitive groove. From this the folding of the two coelom-pouches proceeds in the same way as in the other mammals (cf. Figures 1.96 and 1.97). In the middle of the sole-shaped embryonic shield the first primitive segments immediately begin to make their appearance. At this age the human embryo cannot be distinguished from that of other mammals, such as the hare or dog.

A week later (or after the twenty-first day) the human embryo has doubled its length; it is now about one-fifth of an inch long, and, when seen from the side, shows the characteristic bend of the back, the swelling of the head-end, the first outline of the three higher sense-organs, and the rudiments of the gill-clefts, which pierce the sides of the neck (Figure 1.179, III). The allantois has grown out of the gut behind. The embryo is already entirely enclosed in the amnion, and is only connected in the middle of the belly by the vitelline duct with the embryonic vesicle, which changes into the yelk-sac. There are no extremities or limbs at this stage, no trace of arms or legs. The head-end has been strongly differentiated from the tail-end; and the first outlines of the cerebral vesicles in front, and the heart below, under the fore-arm, are already more or less clearly seen. There is as yet no real face. Moreover, we seek in vain at this stage a special character that may distinguish the human embryo from that of other mammals.

(FIGURE 1.182. Median longitudinal section of the tail of a human embryo, two-thirds of an inch long. (From Ross Granville Harrison.) Med medullary tube, Ca.fil caudal filament, ch chorda, ao caudal artery, V.c.i caudal vein, an a.n.u.s, S.ug sinus urogenitalis.)

A week later (after the fourth week, on the twenty-eighth to thirtieth day of development) the human embryo has reached a length of about one-third of an inch (Figure 1.179 IV). We can now clearly distinguish the head with its various parts; inside it the five primitive cerebral vesicles (fore-brain, middle-brain, intermediate-brain, hind-brain, and after-brain); under the head the gill-arches, which divide the gill-clefts; at the sides of the head the rudiments of the eyes, a couple of pits in the outer skin, with a pair of corresponding simple vesicles growing out of the lateral wall of the fore-brain (Figures 1.180, 1.181 a). Far behind the eyes, over the last gill-arches, we see a vesicular rudiment of the auscultory organ. The rudimentary limbs are now clearly outlined--four simple buds of the shape of round plates, a pair of fore (vg) and a pair of hind legs (hg), the former a little larger than the latter. The large head bends over the trunk, almost at a right angle. The latter is still connected in the middle of its ventral side with the embryonic vesicle; but the embryo has still further severed itself from it, so that it already hangs out as the yelk-sac. The hind part of the body is also very much curved, so that the pointed tail-end is directed towards the head. The head and face-part are sunk entirely on the still open breast. The bend soon increases so much that the tail almost touches the forehead (Figure 1.179 V.; Figure 1.181). We may then distinguish three or four special curves on the round dorsal surface--namely, a skull-curve in the region of the second cerebral vesicle, a neck-curve at the beginning of the spinal cord, and a tail-curve at the fore-end. This p.r.o.nounced curve is only shared by man and the higher cla.s.ses of vertebrates (the amniotes); it is much slighter, or not found at all, in the lower vertebrates. At this age (four weeks) man has a considerable tail, twice as long as his legs. A vertical longitudinal section through the middle plane of this tail (Figure 1.182) shows that the hinder end of the spinal marrow extends to the point of the tail, as also does the underlying chorda (ch), the terminal continuation of the vertebral column. Of the latter, the rudiments of the seven coccygeal (or lowest) vertebrae are visible--thirty-two indicates the third and thirty-six the seventh of these. Under the vertebral column we see the hindmost ends of the two large blood-vessels of the tail, the princ.i.p.al artery (aorta caudalis or arteria sacralis media, Ao), and the princ.i.p.al vein (vena caudalis or sacralis media). Underneath is the opening of the a.n.u.s (an) and the urogenital sinus (S.ug). From this anatomic structure of the human tail it is perfectly clear that it is the rudiment of an ape-tail, the last hereditary relic of a long hairy tail, which has been handed down from our tertiary primate ancestors to the present day.

(FIGURE 1.183. Human embryo, four weeks old, opened on the ventral side. Ventral and dorsal walls are cut away, so as to show the contents of the pectoral and abdominal cavities. All the appendages are also removed (amnion, allantois, yelk-sac), and the middle part of the gut. n eye, 3 nose, 4 upper jaw, 5 lower jaw, 6 second, 6 double apostrophe, third gill-arch, ov heart (o right, o apostrophe, left auricle; v right, v apostrophe, left ventricle), b origin of the aorta, f liver (u umbilical vein), e gut (with vitelline artery, cut off at a apostrophe), j apostrophe, vitelline vein, m primitive kidneys, t rudimentary s.e.xual glands, r terminal gut (cut off at the mesentery z), n umbilical artery, u umbilical vein, 9 fore-leg, 9 apostrophe, hind-leg. (From Coste.)

FIGURE 1.184. Human embryo, five weeks old, opened from the ventral side (as in Figure 1.183). Breast and belly-wall and liver are removed. 3 outer nasal process, 4 upper jaw, 5 lower jaw, z tongue, v right, v apostrophe, left ventricle of heart, o apostrophe, left auricle, b origin of aorta, b apostrophe, b double apostrophe, b triple apostrophe, first, second, and third aorta-arches, c, c apostrophe, c double apostrophe, vena cava, ae lungs (y pulmonary artery), e stomach, m primitive kidneys (j left vitelline vein, s cystic vein, a right vitelline artery, n umbilical artery, u umbilical vein), x vitelline duct, i r.e.c.t.u.m, 8 tail, 9 fore-leg, 9 apostrophe, hind-leg. (From Coste.))

It sometimes happens that we find even external relics of this tail growing. According to the ill.u.s.trated works of Surgeon-General Bernhard Ornstein, of Greece, these tailed men are not uncommon; it is not impossible that they gave rise to the ancient fables of the satyrs. A great number of such cases are given by Max Bartels in his essay on "Tailed Men" (1884, in the Archiv fur Anthropologie, Band 15), and critically examined. These atavistic human tails are often mobile; sometimes they contain only muscles and fat, sometimes also rudiments of caudal vertebrae. They have a length of eight to ten inches and more. Granville Harrison has very carefully studied one of these cases of "pigtail," which he removed by operation from a six months old child in 1901. The tail moved briskly when the child cried or was excited, and was drawn up when at rest.

(FIGURE 1.185. The head of Miss Julia Pastrana. (From a photograph by Hintze.)

FIGURE 1.186. Human ovum of twelve to thirteen days (?). (From Allen Thomson.) 1. Not opened, natural size. 2. Opened and magnified. Within the outer chorion the tiny curved foetus lies on the large embryonic vesicle, to the left above.

FIGURE 1.187. Human ovum of ten days. (From Allen Thomson.) Natural size, opened; the small foetus in the right half, above.

FIGURE 1.188. Human foetus of ten days, taken from the preceding ovum, magnified ten times, a yelk-sac, b neck (the medullary groove already closed), c head (with open medullary groove), d hind part (with open medullary groove), e a shred of the amnion.

FIGURE 1.189. Human ovum of twenty to twenty-two days. (From Allen Thomson.) Natural size, opened. The chorion forms a s.p.a.cious vesicle, to the inner wall of which the small foetus (to the right above) is attached by a short umbilical cord.

FIGURE 1.190. Human foetus of twenty to twenty-two days, taken from the preceding ovum, magnified. a amnion, b yelk-sac, c lower-jaw process of the first gill-arch, d upper-jaw process of same, e second gill-arch (two smaller ones behind). Three gill-clefts are clearly seen. f rudimentary fore-leg, g auditory vesicle, h eye, i heart.)

In the opinion of some travellers and anthropologists, the atavistic tail-formation is hereditary in certain isolated tribes (especially in south-eastern Asia and the archipelago), so that we might speak of a special race or "species" of tailed men (h.o.m.o caudatus). Bartels has "no doubt that these tailed men will be discovered in the advance of our geographical and ethnographical knowledge of the lands in question" (Archiv fur Anthropologie, Band 15 page 129).

When we open a human embryo of one month (Figure 1.183), we find the alimentary ca.n.a.l formed in the body-cavity, and for the most part cut off from the embryonic vesicle. There are both mouth and a.n.u.s apertures. But the mouth-cavity is not yet separated from the nasal cavity, and the face not yet shaped. The heart shows all its four sections; it is very large, and almost fills the whole of the pectoral cavity (Figure 1.183 ov). Behind it are the very small rudimentary lungs. The primitive kidneys (m) are very large; they fill the greater part of the abdominal cavity, and extend from the liver (f) to the pelvic gut. Thus at the end of the first month all the chief organs are already outlined. But there are at this stage no features by which the human embryo materially differs from that of the dog, the hare, the ox, or the horse--in a word, of any other higher mammal. All these embryos have the same, or at least a very similar, form; they can at the most be distinguished from the human embryo by the total size of the body or some other insignificant difference in size. Thus, for instance, in man the head is larger in proportion to the trunk than in the ox. The tail is rather longer in the dog than in man. These are all negligible differences. On the other hand, the whole internal organisation and the form and arrangement of the various organs are essentially the same in the human embryo of four weeks as in the embryos of the other mammals at corresponding stages.

(FIGURE 1.191. Human embryo of sixteen to eighteen days. (From Coste.) Magnified. The embryo is surrounded by the amnion, (a), and lies free with this in the opened embryonic vesicle. The belly is drawn up by the large yelk-sac (d), and fastened to the inner wall of the embryonic membrane by the short and thick pedicle (b). Hence the normal convex curve of the back (Figure 1.190) is here changed into an abnormal concave surface. h heart, m parietal mesoderm. The spots on the outer wall of the serolemma are the roots of the branching chorion-villi, which are free at the border.

FIGURE 1.192. Human embryo of the fourth week, one-third of an inch long, lying in the dissected chorion.

FIGURE 1.193. Human embryo of the fourth week, with its membranes, like Figure 1.192, but a little older. The yelk-sac is rather smaller, the amnion and chorion larger.)

It is otherwise in the second month of human development. Figure 1.179 represents a human embryo of six weeks (VI), one of seven weeks (VII), and one of eight weeks (VIII), at natural size. The differences which mark off the human embryo from that of the dog and the lower mammals now begin to be more p.r.o.nounced. We can see important differences at the sixth, and still more at the eighth week, especially in the formation of the head. The size of the various sections of the brain is greater in man, and the tail is shorter. Other differences between man and the lower mammals are found in the relative size of the internal organs. But even at this stage the human embryo differs very little from that of the nearest related mammals--the apes, especially the anthropomorphic apes. The features by means of which we distinguish between them are not clear until later on. Even at a much more advanced stage of development, when we can distinguish the human foetus from that of the ungulates at a glance, it still closely resembles that of the higher apes. At last we get the distinctive features, and we can distinguish the human embryo confidently at the first glance from that of all other mammals during the last four months of foetal life--from the sixth to the ninth month of pregnancy.

Then we begin to find also the differences between the various races of men, especially in regard to the formation of the skull and the face. (Cf. Chapter 2.23.)

(FIGURE 1.194. Human embryo with its membranes, six weeks old. The outer envelope of the whole ovum is the chorion, thickly covered with its branching villi, a product of the serous membrane. The embryo is enclosed in the delicate amnion-sac. The yelk-sac is reduced to a small pear-shaped umbilical vesicle; its thin pedicle, the long vitelline duct, is enclosed in the umbilical cord. In the latter, behind the vitelline duct, is the much shorter pedicle of the allantois, the inner lamina of which (the gut-gland layer) forms a large vesicle in most of the mammals, while the outer lamina is attached to the inner wall of the outer embryonic coat, and forms the placenta there. (Half diagrammatic.))

The striking resemblance that persists so long between the embryo of man and of the higher apes disappears much earlier in the lower apes.

It naturally remains longest in the large anthropomorphic apes (gorilla, chimpanzee, orang, and gibbon). The physiognomic similarity of these animals, which we find so great in their earlier years, lessens with the increase of age. On the other hand, it remains throughout life in the remarkable long-nosed ape of Borneo (Nasalis larvatus). Its finely-shaped nose would be regarded with envy by many a man who has too little of that organ. If we compare the face of the long-nosed ape with that of abnormally ape-like human beings (such as the famous Miss Julia Pastrana, Figure 1.185), it will be admitted to represent a higher stage of development. There are still people among us who look especially to the face for the "image of G.o.d in man." The long-nosed ape would have more claim to this than some of the stumpy-nosed human individuals one meets.

This progressive divergence of the human from the animal form, which is based on the law of the ontogenetic connection between related forms, is found in the structure of the internal organs as well as in external form. It is also expressed in the construction of the envelopes and appendages that we find surrounding the foetus externally, and that we will now consider more closely. Two of these appendages--the amnion and the allantois--are only found in the three higher cla.s.ses of vertebrates, while the third, the yelk-sac, is found in most of the vertebrates. This is a circ.u.mstance of great importance, and it gives us valuable data for constructing man's genealogical tree.

(FIGURE 1.195. Diagram of the embryonic organs of the mammal (foetal membranes and appendages). (From Turner.) E, M, H outer, middle, and inner germ layer of the embryonic shield, which is figured in median longitudinal section, seen from the left. am amnion. AC amniotic cavity, UV yelk-sac or umbilical vesicle, ALC allantois, al pericoelom or serocoelom (inter-amniotic cavity), sz serolemma (or serous membrane), pc prochorion (with villi).)

As regards the external membrane that encloses the ovum in the mammal womb, we find it just the same in man as in the higher mammals. The ovum is, the reader will remember, first surrounded by the transparent structureless ovolemma or zona pellucida (Figures 1.1 and 1.14). But very soon, even in the first week of development, this is replaced by the permanent chorion. This is formed from the external layer of the amnion, the serolemma, or "serous membrane," the formation of which we shall consider presently; it surrounds the foetus and its appendages as a broad, completely closed sac; the s.p.a.ce between the two, filled with clear watery fluid, is the serocoelom, or interamniotic cavity ("extra-embryonic body-cavity"). But the smooth surface of the sac is quickly covered with numbers of tiny tufts, which are really hollow outgrowths like the fingers of a glove (Figures 1.186, 1.191 and 1.198 chz). They ramify and push into the corresponding depressions that are formed by the tubular glands of the mucous membrane of the maternal womb. Thus, the ovum secures its permanent seat (Figures 1.186 to 1.194).

In human ova of eight to twelve days this external membrane, the chorion, is already covered with small tufts or villi, and forms a ball or spheroid of one-fourth to one-third of an inch in diameter (Figures 1.186 to 1.188). As a large quant.i.ty of fluid gathers inside it, the chorion expands more and more, so that the embryo only occupies a small part of the s.p.a.ce within the vesicle. The villi of the chorion grow larger and more numerous. They branch out more and more. At first the villi cover the whole surface, but they afterwards disappear from the greater part of it; they then develop with proportionately greater vigour at a spot where the placenta is formed from the allantois.

When we open the chorion of a human embryo of three weeks, we find on the ventral side of the foetus a large round sac, filled with fluid.

This is the yelk-sac, or "umbilical vesicle," the origin of which we have considered previously. The larger the embryo becomes the smaller we find the yelk-sac. In the end we find the remainder of it in the shape of a small pear-shaped vesicle, fastened to a long thin stalk (or pedicle), and hanging from the open belly of the foetus (Figure 1.194). This pedicle is the vitelline duct, and is separated from the body at the closing of the navel.

Behind the yelk-sac a second appendage, of much greater importance, is formed at an early stage at the belly of the mammal embryo. This is the allantois or "primitive urinary sac," an important embryonic organ, only found in the three higher cla.s.ses of vertebrates. In all the amniotes the allantois quickly appears at the hinder end of the alimentary ca.n.a.l, growing out of the cavity of the pelvic gut (Figure 1.147 r, u, Figure 1.195 ALC}.

(FIGURE 1.196. Diagrammatic frontal section of the pregnant human womb. (From Longet.) The embryo hangs by the umbilical cord, which encloses the pedicle of the allantois (al). nb umbilical vessel, am amnion, ch chorion, ds decidua serotina, dv decidua vera, dr decidua reflexa, z villi of the placenta, c cervix uteri, u uterus.)

The further development of the allantois varies considerably in the three sub-cla.s.ses of the mammals. The two lower sub-cla.s.ses, monotremes and marsupials, retain the simpler structure of their ancestors, the reptiles. The wall of the allantois and the enveloping serolemma remains smooth and without villi, as in the birds. But in the third sub-cla.s.s of the mammals the serolemma forms, by inv.a.g.i.n.ation at its outer surface, a number of hollow tufts or villi, from which it takes the name of the chorion or mallochorion. The gut-fibre layer of the allantois, richly supplied with branches of the umbilical vessel, presses into these tufts of the primary chorion, and forms the "secondary chorion." Its embryonic blood-vessels are closely correlated to the contiguous maternal blood-vessels of the environing womb, and thus is formed the important nutritive apparatus of the embryo which we call the placenta.