The Evolution of Man, vol 2 - Ernst Haeckel (sight word books .TXT) 📗

(FIGURE 2.217. Transverse section through the middle of the Amphioxus. (From Boveri.) On the left a gill-rod has been struck, and on the right a gill-cleft; consequently on the left we see the whole of a prorenal canal (x), on the right only the section of its fore-leg. A genital chamber (ventral section of the gonocoel), x pronephridium, B its coelom-aperture, C atrium, D body-cavity, E visceral cavity, F subintestinal vein, G aorta (the left branch connected by a branchial vessel with the subintestinal vein), H renal vessel.

FIGURE 2.218. Transverse section of a primitive fish embryo (Selachii-embryo, from Boveri.). To the left pronephridia (B), the right primitive kidneys (A). The dotted lines on the right indicate the later opening of the primitive kidney canals (A) into the prorenal duct (C). D body-cavity, E visceral cavity, F subintestinal vein, G aorta, H renal vessel.)

If we sum up the results of our anatomic study of the Amphioxus, and compare them with the familiar organisation of man, we shall find an immense distance between the two. As a fact, the highest summit of the vertebrate organisation which man represents is in every respect so far above the lowest stage, at which the lancelet remains, that one would at first scarcely believe it possible to class both animals in the same division of the animal kingdom. Nevertheless, this classification is indisputably just. Man is only a more advanced stage of the vertebral type that we find unmistakably in the Amphioxus in its characteristic features. We need only recall the picture of the ideal Primitive Vertebrate given in a former chapter, and compare it with the lower stages of human embryonic development, to convince ourselves of our close relationship to the lancelet. (Cf. Chapter

1.11.)

It is true that the Amphioxus is far below all other living vertebrates. It is true that it has no separate head, no developed brain or skull, the characteristic feature of the other vertebrates. It is (probably as a result of degeneration) without the auscultory organ and the centralised heart that all the others have; and it has no fully-formed kidneys. Every single organ in it is simpler and less advanced than in any of the others. Yet the characteristic connection and arrangement of all the organs is just the same as in the other vertebrates. All these, moreover, pass, during their embryonic development, through a stage in which their whole organisation is no higher than that of the Amphioxus, but is substantially identical with it.

(FIGURE 2.219. Transverse section of the head of the Amphioxus (at the limit of the first and second third of the body). (From Boveri) a aorta (here double), b atrium, c chorda, co umlaut coeloma (body-cavity), e endostyl (hypobranchial groove), g gonads (ovaries), kb gill-arches, kd branchial gut, l liver-tube (on the right, one-sided), m muscles, n renal canals, r spinal cord, sn spinal nerves, sp gill-clefts.)

In order to see this quite clearly, it is particularly useful to compare the Amphioxus with the youthful forms of those vertebrates that are classified next to it. This is the class of the Cyclostoma. There are to-day only a few species of this once extensive class, and these may be distributed in two groups. One group comprises the hag-fishes or Myxinoides. The other group are the Petromyzontes, or lampreys, which are a familiar delicacy in their marine form. These Cyclostoma are usually classified with the fishes. But they are far below the true fishes, and form a very interesting connecting-group between them and the lancelet. One can see how closely they approach the latter by comparing a young lamprey with the Amphioxus. The chorda is of the same simple character in both; also the medullary tube, that lies above the chorda, and the alimentary canal below it. However, in the lamprey the spinal cord swells in front into a simple pear-shaped cerebral vesicle, and at each side of it there are a very simple eye and a rudimentary auditory vesicle. The nose is a single pit, as in the Amphioxus. The two sections of the gut are also just the same and very rudimentary in the lamprey. On the other hand, we see a great advance in the structure of the heart, which is found underneath the gills in the shape of a centralised muscular tube, and is divided into an auricle and a ventricle. Later on the lamprey advances still further, and gets a skull, five cerebral vesicles, a series of independent gill-pouches, etc. This makes all the more interesting the striking resemblance of its immature larva to the developed and sexually mature Amphioxus.

While the Amphioxus is thus connected through the Cyclostoma with the fishes, and so with the series of the higher vertebrates, it is, on the other hand, very closely related to a lowly invertebrate marine animal, from which it seems to be entirely remote at first glance. This remarkable animal is the sea-squirt or Ascidia, which was formerly thought to be closely related to the mussel, and so classed in the molluscs. But since the remarkable embryology of these animals was discovered in 1866, there can be no question that they have nothing to do with the molluscs. To the great astonishment of zoologists, they were found, in their whole individual development, to be closely related to the vertebrates. When fully developed the Ascidiae are shapeless lumps that would not, at first sight, be taken for animals at all. The oval body, frequently studded with knobs or uneven and lumpy, in which we can discover no special external organs, is attached at one end to marine plants, rocks, or the floor of the sea. Many species look like potatoes, others like melon-cacti, others like prunes. Many of the Ascidiae form transparent crusts or deposits on stones and marine plants. Some of the larger species are eaten like oysters. Fishermen, who know them very well, think they are not animals, but plants. They are sold in the fish markets of many of the Italian coast-towns with other lower marine animals under the name of “sea-fruit” (frutti di mare). There is nothing about them to show that they are animals. When they are taken out of the water with the net the most one can perceive is a slight contraction of the body that causes water to spout out in two places. The bulk of the Ascidiae are very small, at the most a few inches long. A few species are a foot or more in length. There are many species of them, and they are found in every sea. As in the case of the Acrania, we have no fossilised remains of the class, because they have no hard and fossilisable parts. However, they must be of great antiquity, and must go back to the primordial epoch.

The name of “Tunicates” is given to the whole class to which the Ascidiae belong, because the body is enclosed in a thick and stiff covering like a mantle (tunica). This mantle—sometimes soft like jelly, sometimes as tough as leather, and sometimes as stiff as cartilage—has a number of peculiarities. The most remarkable of them is that it consists of a woody matter, cellulose—the same vegetal substance that forms the stiff envelopes of the plant-cells, the substance of the wood. The tunicates are the only class of animals that have a real cellulose or woody coat. Sometimes the cellulose mantle is brightly coloured, at other times colourless. Not infrequently it is set with needles or hairs, like a cactus. Often we find a mass of foreign bodies—stone, sand, fragments of mussel-shells, etc.—worked into the mantle. This has earned for the Ascidia the name of “the microcosm.”

(FIGURE 2.220. Organisation of an Ascidia (left view); the dorsal side is turned to the right and the ventral side to the left, the mouth (o) above; the ascidia is attached at the tail end. The branchial gut (br), which is pierced by a number of clefts, continues below in the visceral gut. The rectum opens through the anus (a) into the atrium (cl), from which the excrements are ejected with the respiratory water through the mantle-hole or cloaca (a); m mantle. (From Gegenbaur.)

FIGURE 2.221. Organisation of an Ascidia (as in Figure 2.220, seen from the left). sb branchial sac, v stomach, i small intestine, c heart, t testicle, vd sperm-duct, o ovary, o apostrophe ripe ova in the branchial cavity. The two small arrows indicate the entrance and exit of the water through the openings of the mantle. (From Milne-Edwards.))

The hind end, which corresponds to the tail of the Amphioxus, is usually attached, often by means of regular roots. The dorsal and ventral sides differ a good deal internally, but frequently cannot be distinguished externally. If we open the thick tunic or mantle in order to examine the internal organisation, we first find a spacious cavity filled with water—the mantle-cavity or respiratory cavity (Figure 2.220 cl). It is also called the branchial cavity and the cloaca, because it receives the excrements and sexual products as well as the respiratory water. The greater part of the respiratory cavity is occupied by the large grated branchial sac (br). This is so like the gill-crate of the Amphioxus in its whole arrangement that the resemblance was pointed out by the English naturalist Goodsir, years ago, before anything was known of the relationship of the two animals. As a fact, even in the Ascidia the mouth (o) opens first into this wide branchial sac. The respiratory water passes through the lattice-work of the branchial sac into the branchial cavity, and is ejected from this by the respiratory pore (a apostrophe). Along the ventral side of the branchial sac runs a ciliated groove—the hypobranchial groove which we have previously found at the same spot in the Amphioxus. The food of the Ascidia also consists of tiny organisms, infusoria, diatoms, parts of decomposed marine plants and animals; etc. These pass with the water into the gill-crate and the digestive part of the gut at the end of it, at first into an enlargement of it that represents the stomach. The adjoining small intestine usually forms a loop, bends forward, and opens by an anus (Figure 2.220 a), not directly outwards, but first into the mantle cavity; from this the excrements are ejected by a common outlet (a apostrophe) together with the used-up water and the sexual products. The outlet is sometimes called the branchial pore, and sometimes the cloaca or ejection-aperture. In many of the Ascidiae a glandular mass opens into the gut, and this represents the liver. In some there is another gland besides the liver, and this is taken to represent the kidneys. The body-cavity proper, or coeloma, which is filled with blood and encloses the hepatic gut, is very narrow in the Ascidia, as in the Amphioxus, and is here also usually confounded with the wide atrium, or peribranchial cavity, full of water.

There is no trace in the fully-developed Ascidia of a chorda dorsalis, or internal axial skeleton. It is the more interesting that the young animal that emerges from the ovum HAS a chorda, and that there is a rudimentary medullary tube above it. The latter is wholly atrophied in the developed Ascidia, and looks like a small nerve-ganglion in front above the gill-crate. It corresponds to the upper “gullet-ganglion” or “primitive brain” in other vermalia. Special sense-organs are either wanting altogether or are only found in a very rudimentary form, as simple optic spots and touch-corpuscles or tentacles that surround the mouth. The muscular system is very slightly and irregularly developed. Immediately under the thin corium, and closely connected with it, we find a thin muscle tube, as in the worms. On the other hand, the Ascidia has a centralised heart, and in this respect it seems to be more advanced than the Amphioxus. On the