The Evolution of Man, V.2 by Ernst Haeckel (leveled readers .txt) 📖

can bore its way into the yelk at one pole of the ovum-axis; its head or nucleus coalesces with the female nucleus, which remains after the extrusion of the directive bodies from the germinal vesicle. Thus is formed the "stem-nucleus," or the nucleus of the "stem-cell" (cytula, Figure 1.2). This now undergoes total segmentation, dividing into two, four, eight, sixteen, thirty-two cells, and so on. In this way we get the spherical, mulberry-shaped body, which we call the morula.

The segmentation of the Amphioxus is not entirely regular, as was supposed after the first observations of Kowalevsky (1866). It is not completely equal, but a little unequal. As Hatschek afterwards found (1879), the segmentation-cells only remain equal up to the morula-stage, the spherical body of which consists of thirty-two cells. Then, as always happens in unequal segmentation, the more sluggish vegetal cells are outstripped in the cleavage. At the lower or vegetal pole of the ovum a crown of eight large entodermic cells remains for a long time unchanged, while the other cells divide, owing to the formation of a series of horizontal circles, into an increasing number of crowns of sixteen cells each. Afterwards the segmentation-cells get more or less irregularly displaced, while the segmentation-cavity enlarges in the centre of the morula; in the end the former all lie on the surface of the latter, so that the foetus attains the familiar blastula shape and forms a hollow ball, the wall of which consists of a single stratum of cells (Figure 1.38 A to C). This layer is the blastoderm, the simple epithelium from the cells of which all the tissues of the body proceed.

These important early embryonic processes take place so quickly in the Amphioxus that four or five hours after fecundation, or about midnight, the spherical blastula is completed. A pit-like depression is then formed at the vegetal pole of it, and in consequence of this the hollow sphere doubles on itself (Figure 1.38 D). This pit becomes deeper and deeper (Figure 1.38 E and F); at last the invagination (or doubling) is complete, and the inner or folded part of the blastula-wall lies on the inside of the outer wall. We thus get a hollow hemisphere, the thin wall of which is made up of two layers of cells (Figure 1.38 E). From hemispherical the body soon becomes almost spherical once more, and then oval, the internal cavity enlarging considerably and its mouth growing narrower (Figure 2.213). The form which the Amphioxus-embryo has thus reached is a real "cup-larva" or gastrula, of the original simple type that we have previously described as the "bell-gastrula" or archigastrula (Figures 1.29 to 1.35).

As in all the other animals that form an archigastrula, the whole body is nothing but a simple gastric sac or stomach; its internal cavity is the primitive gut (progaster or archenteron, Figure 1.38 g, 1.35 d), and its aperture the primitive mouth (prostoma or blastoporus, o). The wall is at once gut-wall and body-wall. It is composed of two simple cell-layers, the familiar primary germinal layers. The inner layer or the invaginated part of the blastoderm, which immediately encloses the gut-cavity is the entoderm, the inner or vegetal germ-layer, from which develop the wall of the alimentary canal and all its appendages, the coelom-pouches, etc. (Figures 1.35 and 1.36 i). The outer stratum of cells, or the non-invaginated part of the blastoderm, is the ectoderm, the outer or animal germ-layer, which provides the outer skin (epidermis) and the nervous system (e). The cells of the entoderm are much larger, darker, and more fatty than those of the ectoderm, which are clearer and less rich in fatty particles. Hence before and during invagination there is an increasing differentiation of the inner from the outer layer. The animal cells of the outer layer soon develop vibratory hairs; the vegetal cells of the inner layer do so much later. A thread-like process grows out of each cell, and effects continuous vibratory movements. By the vibrations of these slender hairs the gastrula of the Amphioxus swims about in the sea, when it has pierced the thin ovolemma, like the gastrula of many other animals (Figure 1.36). As in many other lower animals, the cells have only one whip-like hair each, and so are called flagellate (whip) cells (in contrast with the ciliated cells, which have a number of short lashes or cilia).

In the further course of its rapid development the roundish bell-gastrula becomes elongated, and begins to flatten on one side, parallel to the long axis. The flattened side is the subsequent dorsal side; the opposite or ventral side remains curved. The latter grows more quickly than the former, with the result that the primitive mouth is forced to the dorsal side (Figure 1.39). In the middle of the dorsal surface a shallow longitudinal groove or furrow is formed (Figure 1.79), and the edges of the body rise up on each side of this groove in the shape of two parallel swellings. This groove is, of course, the dorsal furrow, and the swellings are the dorsal or medullary swellings; they form the first structure of the central nervous system, the medullary tube. The medullary swellings now rise higher; the groove between them becomes deeper and deeper. The edges of the parallel swellings curve towards each other, and at last unite, and the medullary tube is formed (Figures 1.83 m and 1.84 m). Hence the formation of a medullary tube out of the outer skin takes place in the naked dorsal surface of the free-swimming larva of the Amphioxus in just the same way as we have found in the embryo of man and the higher animals within the foetal membranes.

Simultaneously with the construction of the medullary tube we have in the Amphioxus-embryo the formation of the chorda, the coelom-pouches, and the mesoderm proceeding from their wall. These processes also take place with characteristic simplicity and clearness, so that they are very instructive to compare with the vermalia on the one hand and with the higher vertebrates on the other. While the medullary groove is sinking in the middle line of the flat dorsal side of the oval embryo, and its parallel edges unite to form the ectodermic neural tube, the single chorda is formed directly underneath them, and on each side of this a parallel longitudinal fold, from the dorsal wall of the primitive gut. These longitudinal folds of the entoderm proceed from the primitive mouth, or from its lower and hinder edge. Here we see at an early stage a couple of large entodermic cells, which are distinguished from all the others by their great size, round form, and fine-grained protoplasm; they are the two promesoblasts, or polar cells of the mesoderm (Figure 1.83 p). They indicate the original starting-point of the two coelom-pouches, which grow from this spot between the inner and outer germinal layers, sever themselves from the primitive gut, and provide the cellular material for the middle layer.

Immediately after their formation the two coelom-pouches of the Amphioxus are divided into several parts by longitudinal and transverse folds. Each of the primary pouches is divided into an upper dorsal and a lower ventral section by a couple of lateral longitudinal folds (Figure 1.82). But these are again divided by several parallel transverse folds into a number of successive sacs, the primitive segments or somites (formerly called by the unsuitable name of "primitive vertebrae"). They have a different future above and below. The upper or dorsal segments, the episomites, lose their cavity later on, and form with their cells the muscular plates of the trunk. The lower or ventral segments, the hyposomites, corresponding to the lateral plates of the craniote-embryo, fuse together in the upper part owing to the disappearance of their lateral walls, and thus form the later body-cavity (metacoel); in the lower part they remain separate, and afterwards form the segmental gonads.

In the middle, between the two lateral coelom-folds of the primitive gut, a single central organ detaches from this at an early stage in the middle line of its dorsal wall. This is the dorsal chorda (Figures 1.83 and 1.84 ch). This axial rod, which is the first foundation of the later vertebral column in all the vertebrates, and is the only representative of it in the Amphioxus, originates from the entoderm.

In consequence of these important folding-processes in the primitive gut, the simple entodermic tube divides into four different sections:--

underneath, at the ventral side, the permanent alimentary canal or permanent gut; above, at the dorsal side, the axial rod or chorda; and the two coelom-sacs, which immediately sub-divide into two structures:--

3A. above, on the dorsal side, the episomites, the double row of primitive or muscular segments; and

3B. below, on each side of the gut, the hyposomites, the two lateral plates that give rise to the sex-glands, and the cavities of which partly unite to form the body-cavity. At the same time, the neural or medullary tube is formed above the chorda, on the dorsal surface, by the closing of the parallel medullary swellings.

All these processes, which outline the typical structure of the vertebrate, take place with astonishing rapidity in the embryo of the Amphioxus; in the afternoon of the first day, or twenty-four hours after fertilisation, the young vertebrate, the typical embryo, is formed; it then has, as a rule, six to eight somites.

The chief occurrence on the second day of development is the construction of the two permanent openings of the gut--the mouth and anus. In the earlier stages the alimentary tube is found to be entirely closed, after the closing of the primitive mouth; it only communicates behind by the neurenteric canal with the medullary tube. The permanent mouth is a secondary formation, at the opposite end. Here, at the end of the second day, we find a pit-like depression in the outer skin, which penetrates inwards into the closed gut. The anus is formed behind in the same way a few hours later (in the vicinity of the additional gastrula-mouth). In man and the higher vertebrates also the mouth and anus are formed, as we have seen, as flat pits in the outer skin; they then penetrate inwards, gradually becoming connected with the blind ends of the closed gut-tube. During the second day the Amphioxus-embryo undergoes few other changes. The number of primitive segments increases, and generally amounts to fourteen, some forty-eight to fifty hours after impregnation.

Almost simultaneously with the formation of the mouth the first gill-cleft breaks through in the fore section of the Amphioxus-embryo (generally forty hours after the commencement of development). It now begins to nourish itself independently, as the food material stored up in the ovum is completely used up. The further development of the free larvae takes place very slowly, and extends over several months. The body becomes much longer, and is compressed at the sides, the head-end being broadened in a sort of triangle. Two rudimentary sense-organs are developed in it. Inside we find the first blood-vessels, an upper or dorsal vessel, corresponding to the aorta, between the gut and the dorsal cord, and a lower or ventral vessel, corresponding to the subintestinal vein, at the lower border of the gut. Now, the gills or respiratory organs also are formed at the fore-end of the alimentary canal. The whole of the anterior or respiratory section of the gut is converted into a gill-crate, which is pierced trellis-wise by numbers of branchial-holes, as in the ascidia. This is done by the foremost part of the gut-wall joining star-wise with the outer skin, and the formation of clefts at the point of connection, piercing the wall and leading into the gut from without. At first there are very few of these branchial clefts; but there are soon a number of them--first in one, then in two, rows. The foremost gill-cleft is the oldest. In the end we have a sort of lattice work of fine gill-clefts, supported on a number of stiff branchial rods; these are connected in pairs by transverse