When we have thus declared the vertebrates and the articulates to be the most important and most advanced of the twelve stems of the animal kingdom, the question arises whether this special position is accorded to them on the ground of a peculiarity of organisation that is common to the two. The answer is that this is really the case; it is their segmental or transverse articulation, which we may briefly call metamerism. In all the vertebrates and articulates the developed individual consists of a series of successive members (segments or metamera = "parts"); in the embryo these are called primitive segments or somites. In each of these segments we have a certain group of organs reproduced in the same arrangement, so that we may regard each segment as an individual unity, or a special "individual" subordinated to the entire personality.

The similarity of their segmentation, and the consequent physiological advance in the two stems of the vertebrates and articulates, has led to the a.s.sumption of a direct affinity between them, and an attempt to derive the former directly from the latter. The annelids were supposed to be the direct ancestors, not only of the crustacea and tracheata, but also of the vertebrates. We shall see later (Chapter 2.20) that this annelid theory of the vertebrates is entirely wrong, and ignores the most important differences in the organisation of the two stems.

The internal articulation of the vertebrates is just as profoundly different from the external metamerism of the articulates as are their skeletal structure, nervous system, vascular system, and so on. The articulation has been developed in a totally different way in the two stems. The unarticulated chordula (Figures 1.83 to 1.86), which we have recognised as one of the chief palingenetic embryonic forms of the vertebrate group, and from which we have inferred the existence of a corresponding ancestral form for all the vertebrates and tunicates, is quite unthinkable as the stem-form of the articulates.

All articulated animals came originally from unarticulated ones. This phylogenetic principle is as firmly established as the ontogenetic fact that every articulated animal-form develops from an unarticulated embryo. But the organisation of the embryo is totally different in the two stems. The chordula-embryo of all the vertebrates is characterised by the dorsal medullary tube, the neurenteric ca.n.a.l, which pa.s.ses at the primitive mouth into the alimentary ca.n.a.l, and the axial chorda between the two. None of the articulates, either annelids or arthropods (crustacea and tracheata), show any trace of this type of organisation. Moreover, the development of the chief systems of organs proceeds in the opposite way in the two stems. Hence the segmentation must have arisen independently in each. This is not at all surprising; we find a.n.a.logous cases in the stalk-articulation of the higher plants and in several groups of other animal stems.

The characteristic internal articulation of the vertebrates and its importance in the organisation of the stem are best seen in the study of the skeleton. Its chief and central part, the cartilaginous or bony vertebral column, affords an obvious instance of vertebrate metamerism; it consists of a series of cartilaginous or bony pieces, which have long been known as vertebrae (or spondyli). Each vertebra is directly connected with a special section of the muscular system, the nervous system, the vascular system, etc. Thus most of the "animal organs" take part in this vertebration. But we saw, when we were considering our own vertebrate character (in Chapter 1.11), that the same internal articulation is also found in the lowest primitive vertebrates, the acrania, although here the whole skeleton consists merely of the simple chorda, and is not at all articulated. Hence the articulation does not proceed primarily from the skeleton, but from the muscular system, and is clearly determined by the more advanced swimming-movements of the primitive chordonia-ancestors.

(FIGURES 1.153 TO 1.155. Sole-shaped embryonic disk of the chick, in three successive stages of development, looked at from the dorsal surface, magnified about twenty times, somewhat diagrammatic. Figure 1.153 with six pairs of somites. Brain a simple vesicle (hb).

Medullary furrow still wide open from x; greatly widened at z. mp medullary plates, sp lateral plates, y limit of gullet-cavity (sh) and fore-gut (vd). Figure 1.154 with ten pairs of somites. Brain divided into three vesicles: v fore-brain, m middle-brain, h hind-brain, c heart, dv vitelline-veins. Medullary furrow still wide open behind (z). mp medullary plates. Figure 1.155 with sixteen pairs of somites.

Brain divided into five vesicles: v fore-brain, z intermediate-brain, m middle-brain, h hind-brain, n after-brain, a optic vesicles, g auditory vesicles, c heart, dv vitelline veins, mp medullary plate, uw primitive vertebra.)

It is, therefore, wrong to describe the first rudimentary segments in the vertebrate embryo as primitive vertebrae or provertebrae; the fact that they have been so called for some time has led to much error and misunderstanding. Hence we shall give the name of "somites" or primitive segments to these so-called "primitive vertebrae." If the latter name is retained at all, it should only be used of the sclerotom--i.e., the small part of the somites from which the later vertebra does actually develop.

Articulation begins in all vertebrates at a very early embryonic stage, and this indicates the considerable phylogenetic age of the process. When the chordula (Figures 1.83 to 1.86) has completed its characteristic composition, often even a little earlier, we find in the amniotes, in the middle of the sole-shaped embryonic shield, several pairs of dark square spots, symmetrically distributed on both sides of the chorda (Figures 1.131 to 1.135). Transverse sections (Figure 1.93 uw) show that they belong to the stem-zone (episoma) of the mesoderm, and are separated from the parietal zone (hyposoma) by the lateral folds; in section they are still quadrangular, almost square, so that they look something like dice. These pairs of "cubes"

of the mesoderm are the first traces of the primitive segments or somites, the so-called "protovertebrae." (Figures 1.153 to 1.155 uw).

(FIGURE 1.156. Embryo of the amphioxus, sixteen hours old, seen from the back. (From Hatschek.) d primitive gut, u primitive mouth, p polar cells of the mesoderm, c coelom-pouches, m their first segment, n medullary tube, i entoderm, e ectoderm, s first segment-fold.

FIGURE 1.157. Embryo of the amphioxus, twenty hours old, with five somites. (Right view; for left view see Figure 1.124.) (From Hatschek.) V fore end, H hind end. ak, mk, ik outer, middle, and inner germinal layers; dh alimentary ca.n.a.l, n neural tube, cn ca.n.a.lis neurentericus, ush coelom-pouches (or primitive-segment cavities), us1 first (and foremost) primitive segment.)

Among the mammals the embryos of the marsupials have three pairs of somites (Figure 1.131) after sixty hours, and eight pairs after seventy-two hours (Figure 1.135). They develop more slowly in the embryo of the rabbit; this has three somites on the eighth day (Figure 1.132), and eight somites a day later (Figure 1.134). In the incubated hen's egg the first somites make their appearance thirty hours after incubation begins (Figure 1.153). At the end of the second day the number has risen to sixteen or eighteen (Figure 1.155). The articulation of the stem-zone, to which the somites owe their origin, thus proceeds briskly from front to rear, new transverse constrictions of the "protovertebral plates" forming continuously and successively.

The first segment, which is almost half-way down in the embryonic shield of the amniote, is the foremost of all; from this first somite is formed the first cervical vertebra with its muscles and skeletal parts. It follows from this, firstly, that the multiplication of the primitive segments proceeds backwards from the front, with a constant lengthening of the hinder end of the body; and, secondly, that at the beginning of segmentation nearly the whole of the anterior half of the sole-shaped embryonic shield of the amniote belongs to the later head, while the whole of the rest of the body is formed from its hinder half. We are reminded that in the amphioxus (and in our hypothetic primitive vertebrate, Figures 1.98 to 1.102) nearly the whole of the fore half corresponds to the head, and the hind half to the trunk.

The number of the metamera, and of the embryonic somites or primitive segments from which they develop, varies considerably in the vertebrates, according as the hind part of the body is short or is lengthened by a tail. In the developed man the trunk (including the rudimentary tail) consists of thirty-three metamera, the solid centre of which is formed by that number of vertebrae in the vertebral column (seven cervical, twelve dorsal, five lumbar, five sacral, and four caudal). To these we must add at least nine head-vertebrae, which originally (in all the craniota) const.i.tute the skull. Thus the total number of the primitive segments of the human body is raised to at least forty-two; it would reach forty-five to forty-eight if (according to recent investigations) the number of the original segments of the skull is put at twelve to fifteen. In the tailless or anthropoid apes the number of metamera is much the same as in man, only differing by one or two; but it is much larger in the long-tailed apes and most of the other mammals. In long serpents and fishes it reaches several hundred (sometimes 400).

(FIGURES 1.158 TO 1.160. Embryo of the amphioxus, twenty four hours old, with eight somites. (From Hatschek.) Figures 1.158 and 1.159 lateral view (from left). Figure 1.160 seen from back. In Figure 1.158 only the outlines of the eight primitive segments are indicated, in Figure 1.159 their cavities and muscular walls. V fore end, H hind end, d gut, du under and dd upper wall of the gut, ne ca.n.a.lis neurentericus, nv ventral, nd dorsal wall of the neural tube, np neuroporus, dv fore pouch of the gut, ch chorda, mf mesodermic fold, pm polar cells of the mesoderm (ms), e ectoderm.)

In order to understand properly the real nature and origin of articulation in the human body and that of the higher vertebrates, it is necessary to compare it with that of the lower vertebrates, and bear in mind always the genetic connection of all the members of the stem. In this the simple development of the invaluable amphioxus once more furnishes the key to the complex and cenogenetically modified embryonic processes of the craniota. The articulation of the amphioxus begins at an early stage--earlier than in the craniotes. The two coelom-pouches have hardly grown out of the primitive gut (Figure 1.156 c) when the blind fore part of it (farthest away from the primitive mouth, u) begins to separate by a transverse fold (s): this is the first primitive segment. Immediately afterwards the hind part of the coelom-pouches begins to divide into a series of pieces by new transverse folds (Figure 1.157). The foremost of these primitive segments (us1) is the first and oldest; in Figures 1.124 and 1.157 there are already five formed. They separate so rapidly, one behind the other, that eight pairs are formed within twenty-four hours of the beginning of development, and seventeen pairs twenty-four hours later.

The number increases as the embryo grows and extends backwards, and new cells are formed constantly (at the primitive mouth) from the two primitive mesodermic cells (Figures 1.159 to 1.160).

(FIGURES 1.161 AND 1.162. Transverse section of shark-embryos (through the region of the kidneys). (From Wijhe and Hertwig.) In Figure 1.162 the dorsal segment-cavities (h) are already separated from the body-cavity (lh), but they are connected a little earlier (Figure 1.161), nr neural tube, ch chorda, sch subchordal string, ao aorta, sk skeletal-plate, mp muscle-plate, cp cutis-plate, w connection of latter (growth-zone), vn primitive kidneys, ug prorenal duct, uk prorenal ca.n.a.ls, us point where they are cut off, tr prorenal funnel, mk middle germ-layer (mk1 parietal, mk2 visceral), ik inner germ-layer (gut-gland layer).)

This typical articulation of the two coelom-sacs begins very early in the lancelet, before they are yet severed from the primitive gut, so that at first each segment-cavity (us) still communicates by a narrow opening with the gut, like an intestinal gland. But this opening soon closes by complete severance, proceeding regularly backwards. The closed segments then extend more, so that their upper half grows upwards like a fold between the ectoderm (ak) and neural tube (n), and the lower half between the ectoderm and alimentary ca.n.a.l (ch; Figure 1.82 d, left half of the figure). Afterwards the two halves completely separate, a lateral longitudinal fold cutting between them (mk, right half of Figure 1.82). The dorsal segments (sd) provide the muscles of the trunk the whole length of the body (1.159): this cavity afterwards disappears. On the other hand, the ventral parts give rise, from their uppermost section, to the p.r.o.nephridia or primitive-kidney ca.n.a.ls, and from the lower to the segmental rudiments of the s.e.xual glands or gonads. The part.i.tions of the muscular dorsal pieces (myotomes) remain, and determine the permanent articulation of the vertebrate organism. But the part.i.tions of the large ventral pieces (gonotomes) become thinner, and afterwards disappear in part, so that their cavities run together to form the metacoel, or the simple permanent body-cavity.

The articulation proceeds in substantially the same way in the other vertebrates, the craniota, starting from the coelom-pouches. But whereas in the former case there is first a transverse division of the coelom-sacs (by vertical folds) and then the dorso-ventral division, the procedure is reversed in the craniota; in their case each of the long coelom-pouches first divides into a dorsal (primitive segment plates) and a ventral (lateral plates) section by a lateral longitudinal fold. Only the former are then broken up into primitive segments by the subsequent vertical folds; while the latter (segmented for a time in the amphioxus) remain undivided, and, by the divergence of their parietal and visceral plates, form a body-cavity that is unified from the first. In this case, again, it is clear that we must regard the features of the younger craniota as cenogenetically modified processes that can be traced palingenetically to the older acrania.

We have an interesting intermediate stage between the acrania and the fishes in these and many other respects in the cyclostoma (the hag and the lamprey, cf. Chapter 2.21).

(FIGURE 1.163. Frontal (or horizontal-longitudinal) section of a triton-embryo with three pairs of primitive segments. ch chorda, us primitive segments, ush their cavity, ak horn plate.)

Among the fishes the selachii, or primitive fishes, yield the most important information on these and many other phylogenetic questions (Figures 1.161 and 1.162). The careful studies of Ruckert, Van Wijhe, H.E. Ziegler, and others, have given us most valuable results. The products of the middle germinal layer are partly clear in these cases at the period when the dorsal primitive segment cavities (or myocoels, h) are still connected with the ventral body-cavity (lh; Figure 1.161). In Figure 1.162, a somewhat older embryo, these cavities are separated. The outer or lateral wall of the dorsal segment yields the cutis-plate (cp), the foundation of the connective corium. From its inner or median wall are developed the muscle-plate (mp, the rudiment of the trunk-muscles) and the skeletal plate, the formative matter of the vertebral column (sk).

In the amphibia, also, especially the water-salamander (Triton), we can observe very clearly the articulation of the coelom-pouches and the rise of the primitive segments from their dorsal half (cf. Figure 1.91, A, B, C). A horizontal longitudinal section of the salamander-embryo (Figure 1.163) shows very clearly the series of pairs of these vesicular dorsal segments, which have been cut off on each side from the ventral side-plates, and lie to the right and left of the chorda.

(FIGURE 1.164. The third cervical vertebra (human).

FIGURE 1.165. The sixth dorsal vertebra (human).

FIGURE 1.166. The second lumbar vertebra (human).)

The metamerism of the amniotes agrees in all essential points with that of the three lower cla.s.ses of vertebrates we have considered; but it varies considerably in detail, in consequence of cenogenetic disturbances that are due in the first place (like the degeneration of the coelom-pouches) to the large development of the food-yelk. As the pressure of this seems to force the two middle layers together from the start, and as the solid structure of the mesoderm apparently belies the original hollow character of the sacs, the two sections of the mesoderm, which are at that time divided by the lateral fold--the dorsal segment-plates and ventral side-plates--have the appearance at first of solid layers of cells (Figures 1.94 to 1.97). And when the articulation of the somites begins in the sole-shaped embryonic shield, and a couple of protovertebrae are developed in succession, constantly increasing in number towards the rear, these cube-shaped somites (formerly called protovertebrae, or primitive vertebrae) have the appearance of solid dice, made up of mesodermic cells (Figure 1.93). Nevertheless, there is for a time a ventral cavity, or provertebral cavity, even in these solid "protovertebrae" (Figure 1.143 uwh). This vesicular condition of the provertebra is of the greatest phylogenetic interest; we must, according to the coelom theory, regard it as an hereditary reproduction of the hollow dorsal somites of the amphioxus (Figures 1.156 to 1.160) and the lower vertebrates (Figures 1.161 to 1.163). This rudimentary "provertebral cavity" has no physiological significance whatever in the amniote-embryo; it soon disappears, being filled up with cells of the muscular plate.

(FIGURE 1.167. Head of a shark embryo (Pristiurus), one-third of an inch long, magnified twenty times. (From Parker.) Seen from the ventral side.)

The innermost median part of the primitive segment plates, which lies immediately on the chorda (Figure 1.145 ch) and the medullary tube (m), forms the vertebral column in all the higher vertebrates (it is wanting in the lowest); hence it may be called the skeleton plate. In each of the provertebrae it is called the "sclerotome" (in opposition to the outlying muscular plate, the "myotome"). From the phylogenetic point of view the myotomes are much older than the sclerotomes. The lower or ventral part of each sclerotome (the inner and lower edge of the cube-shaped provertebra) divides into two plates, which grow round the chorda, and thus form the foundation of the body of the vertebra (wh). The upper plate presses between the chorda and the medullary tube, the lower between the chorda and the alimentary ca.n.a.l (Figure 1.137 C). As the plates of two opposite provertebral pieces unite from the right and left, a circular sheath is formed round this part of the chorda. From this develops the BODY of a vertebra--that is to say, the ma.s.sive lower or ventral half of the bony ring, which is called the "vertebra" proper and surrounds the medullary tube (Figures 1.164 to 1.166). The upper or dorsal half of this bony ring, the vertebral arch (Figure 1.145 wb), arises in just the same way from the upper part of the skeletal plate, and therefore from the inner and upper edge of the cube-shaped primitive vertebra. As the upper edges of two opposing somites grow together over the medullary tube from right and left, the vertebra-arch becomes closed.

The whole of the secondary vertebra, which is thus formed from the union of the skeletal plates of two provertebral pieces and encloses a part of the chorda in its body, consists at first of a rather soft ma.s.s of cells; this afterwards pa.s.ses into a firmer, cartilaginous stage, and finally into a third, permanent, bony stage. These three stages can generally be distinguished in the greater part of the skeleton of the higher vertebrates; at first most parts of the skeleton are soft, tender, and membranous; they then become cartilaginous in the course of their development, and finally bony.

(FIGURES 1.168 AND 1.169. Head of a chick embryo, of the third day.

Figure 1.168 from the front, Figure 1.169 from the right. n rudimentary nose (olfactory pit), l rudimentary eye (optic pit, lens-cavity), g rudimentary ear (auditory pit), v fore-brain, gl eye-cleft. Of the three pairs of gill-arches the first has pa.s.sed into a process of the upper jaw (o) and of the lower jaw (u). (From Kolliker.))

At the head part of the embryo in the amniotes there is not generally a cleavage of the middle germinal layer into provertebral and lateral plates, but the dorsal and ventral somites are blended from the first, and form what are called the "head-plates" (Figure 1.148 k). From these are formed the skull, the bony case of the brain, and the muscles and corium of the body. The skull develops in the same way as the membranous vertebral column. The right and left halves of the head curve over the cerebral vesicle, enclose the foremost part of the chorda below, and thus finally form a simple, soft, membranous capsule about the brain. This is afterwards converted into a cartilaginous primitive skull, such as we find permanently in many of the fishes.

Much later this cartilaginous skull becomes the permanent bony skull with its various parts. The bony skull in man and all the other amniotes is more highly differentiated and modified than that of the lower vertebrates, the amphibia and fishes. But as the one has arisen phylogenetically from the other, we must a.s.sume that in the former no less than the latter the skull was originally formed from the sclerotomes of a number of (at least nine) head-somites.

While the articulation of the vertebrate body is always obvious in the episoma or dorsal body, and is clearly expressed in the segmentation of the muscular plates and vertebrae, it is more latent in the hyposoma or ventral body. Nevertheless, the hyposomites of the vegetal half of the body are not less important than the episomites of the animal half. The segmentation in the ventral cavity affects the following princ.i.p.al systems of organs: 1, the gonads or s.e.x-glands (gonotomes); 2, the nephridia or kidneys (nephrotomes); and 3, the head-gut with its gill-clefts (branchiotomes).

(FIGURE 1.170. Head of a dog embryo, seen from the front. a the two lateral halves of the foremost cerebral vesicle, b rudimentary eye, c middle cerebral vesicle, de first pair of gill-arches (e upper-jaw process, d lower-jaw process), f, f apostrophe, f double apostrophe, second, third, and fourth pairs of gill-arches, g h i k heart (g right, h left auricle; i left, k right ventricle), l origin of the aorta with three pairs of arches, which go to the gill-arches. (From Bischoff.))

The metamerism of the hyposoma is less conspicuous because in all the craniotes the cavities of the ventral segments, in the walls of which the s.e.xual products are developed, have long since coalesced, and formed a single large body-cavity, owing to the disappearance of the part.i.tion. This cenogenetic process is so old that the cavity seems to be unsegmented from the first in all the craniotes, and the rudiment of the gonads also is almost always unsegmented. It is the more interesting to learn that, according to the important discovery of Ruckert, this s.e.xual structure is at first segmental even in the actual selachii, and the several gonotomes only blend into a simple s.e.xual gland on either side secondarily.

(FIGURE 1.171. Human embryo of the fourth week (twenty-six days old), one-fourth of an inch in length magnified twenty times, showing: point of development of the hind-leg, umbilical cord (underneath it the tail, bent upwards), trigeminal nerve V Trigeminus, optic-muscle nerve III Oculo-motorius, rolling muscle nerve IV Trochlearis, rudiment of ear (labyrinthic vesicles), pneumogastric nerve X Vagus, terminal nerve XI Accessorius, hypoglossal nerve XII Hypoglossus, first spinal nerve, point of development of arm (or fore-leg), true spinal nerve.

(From Moll.) The rudiments of the cerebral nerves and the roots of the spinal nerves are especially marked. Underneath the four gill-arches (left side) is the heart (with auricle, V and ventricle, K), under this again the liver (L).)

Amphioxus, the sole surviving representative of the acrania, once more yields us most interesting information; in this case the s.e.xual glands remain segmented throughout life. The s.e.xually mature lancelet has, on the right and left of the gut, a series of metamerous sacs, which are filled with ova in the female and sperm in the male. These segmental gonads are originally nothing else than the real gonotomes, separate body-cavities, formed from the hyposomites of the trunk.

The gonads are the most important segmental organs of the hyposoma, in the sense that they are phylogenetically the oldest. We find s.e.xual glands (as pouch-like appendages of the gastro-ca.n.a.l system) in most of the lower animals, even in the medusae, etc., which have no kidneys. The latter appear first (as a pair of excretory tubes) in the platodes (turbellaria), and have probably been inherited from these by the articulates (annelids) on the one hand and the unarticulated prochordonia on the other, and from these pa.s.sed to the articulated vertebrates. The oldest form of the kidney system in this stem are the segmental p.r.o.nephridia or prorenal ca.n.a.ls, in the same arrangement as Boveri found them in the amphioxus. They are small ca.n.a.ls that lie in the frontal plane, on each side of the chorda, between the episoma and hyposoma (Figure 1.102 n); their internal funnel-shaped opening leads into the various body-cavities, their outer opening is the lateral furrow of the epidermis. Originally they must have had a double function, the carrying away of the urine from the episomites and the release of the s.e.xual cells from the hyposomites.

The recent investigations of Ruckert and Van Wijhe on the mesodermic segments of the trunk and the excretory system of the selachii show that these "primitive fishes" are closely related to the amphioxus in this further respect. The transverse section of the shark-embryo in Figure 1.161 shows this very clearly.

In other higher vertebrates, also, the kidneys develop (though very differently formed later on) from similar structures, which have been secondarily derived from the segmental p.r.o.nephridia of the acrania.

The parts of the mesoderm at which the first traces of them are found are usually called the middle or mesenteric plates. As the first traces of the gonads make their appearance in the lining of these middle plates nearer inward (or the middle) from the inner funnels of the nephro-ca.n.a.ls, it is better to count this part of the mesoderm with the hyposoma.

The chief and oldest organ of the vertebrate hyposoma, the alimentary ca.n.a.l, is generally described as an unsegmented organ. But we could just as well say that it is the oldest of all the segmented organs of the vertebrate; the double row of the coelom-pouches grows out of the dorsal wall of the gut, on either side of the chorda. In the brief period during which these segmental coelom-pouches are still openly connected with the gut, they look just like a double chain of segmented visceral glands. But apart from this, we have originally in all vertebrates an important articulation of the fore-gut, that is wanting in the lower gut, the segmentation of the branchial (gill) gut.

(FIGURE 1.172. Transverse section of the shoulder and fore-limb (wing) of a chick-embryo of the fourth day, magnified about twenty times.

Beside the medullary tube we can see on each side three clear streaks in the dark dorsal wall, which advance into the rudimentary fore-limb or wing (e). The uppermost of them is the muscular plate; the middle is the hind and the lowest the fore root of a spinal nerve. Under the chorda in the middle is the single aorta, at each side of it a cardinal vein, and below these the primitive kidneys. The gut is almost closed. The ventral wall advances into the amnion, which encloses the embryo. (From Remak.)

FIGURE 1.173. Transverse section of the pelvic region and hind legs of a chick-embryo of the fourth day, magnified about forty times. h horn-plate, w medullary tube, n ca.n.a.l of the tube, u primitive kidneys, x chorda, e hind legs, b allantoic ca.n.a.l in the ventral wall, t aorta, v cardinal veins, a gut, d gut-gland layer, f gut-fibre layer, g embryonic epithelium, r dorsal muscles, c body-cavity or coeloma. (From Waldeyer.))

The gill-clefts, which originally in the older acrania pierced the wall of the fore-gut, and the gill-arches that separated them, were presumably also segmental, and distributed among the various metamera of the chain, like the gonads in the after-gut and the nephridia. In the amphioxus, too, they are still segmentally formed. Probably there was a division of labour of the hyposomites in the older (and long extinct) acrania, in such wise that those of the fore-gut took over the function of breathing and those of the after-gut that of reproduction. The former developed into gill-pouches, the latter into s.e.x-pouches. There may have been primitive kidneys in both. Though the gills have lost their function in the higher animals, certain parts of them have been generally maintained in the embryo by a tenacious heredity. At a very early stage we notice in the embryo of man and the other amniotes, at each side of the head, the remarkable and important structures which we call the gill-arches and gill-clefts (Figures 1.167 to 1.170 f). They belong to the characteristic and inalienable organs of the amniote-embryo, and are found always in the same spot and with the same arrangement and structure. There are formed to the right and left in the lateral wall of the fore-gut cavity, in its foremost part, first a pair and then several pairs of sac-shaped inlets, that pierce the whole thickness of the lateral wall of the head. They are thus converted into clefts, through which one can penetrate freely from without into the gullet. The wall thickens between these branchial folds, and changes into an arch-like or sickle-shaped piece--the gill, or gullet-arch. In this the muscles and skeletal parts of the branchial gut separate; a blood-vessel arch rises afterwards on their inner side (Figure 1.98 ka). The number of the branchial arches and the clefts that alternate with them is four or five on each side in the higher vertebrates (Figure 1.170 d, f, f apostrophe, f double apostrophe). In some of the fishes (selachii) and in the cyclostoma we find six or seven of them permanently.

These remarkable structures had originally the function of respiratory organs--gills. In the fishes the water that serves for breathing, and is taken in at the mouth, still always pa.s.ses out by the branchial clefts at the sides of the gullet. In the higher vertebrates they afterwards disappear. The branchial arches are converted partly into the jaws, partly into the bones of the tongue and the ear. From the first gill-cleft is formed the tympanic cavity of the ear.

There are few parts of the vertebrate organism that, like the outer covering or integument of the body, are not subject to metamerism. The outer skin (epidermis) is unsegmented from the first, and proceeds from the continuous h.o.r.n.y plate. Moreover, the underlying cutis is also not metamerous, although it develops from the segmental structure of the cutis-plates (Figures 1.161 and 1.162 cp). The vertebrates are strikingly and profoundly different from the articulates in these respects also.

Further, most of the vertebrates still have a number of unarticulated organs, which have arisen locally, by adaptation of particular parts of the body to certain special functions. Of this character are the sense-organs in the episoma, and the limbs, the heart, the spleen, and the large visceral glands--lungs, liver, pancreas, etc.--in the hyposoma. The heart is originally only a local spindle-shaped enlargement of the large ventral blood-vessel or princ.i.p.al vein, at the point where the subintestinal pa.s.ses into the branchial artery, at the limit of the head and trunk (Figures 1.170 and 1.171). The three higher sense-organs--nose, eye, and ear--were originally developed in the same form in all the craniotes, as three pairs of small depressions in the skin at the side of the head.

The organ of smell, the nose, has the appearance of a pair of small pits above the mouth-aperture, in front of the head (Figure 1.169 n).