The Evolution of Man, vol 2, Ernst Haeckel [online e reader txt] 📗

The theory afterwards received a good deal of support from the research made by a number of distinguished zoologists and anatomists, especially C. Kupffer, B. Hatschek, F. Balfour, E. Van Beneden, and Julin. Since Hatschek’s Studies of the Development of the Amphioxus gave us full information as to the embryology of this lowest vertebrate, it has become so important for our purpose that we must consider it a document of the first rank for answering the question we are dealing with.

The ontogenetic facts that we gather from this sole survivor of the Acrania are the more valuable for phylogenetic purposes, as paleontology, unfortunately, throws no light whatever on the origin of the Vertebrates. Their invertebrate ancestors were soft organisms without skeleton, and thus incapable of fossilisation, as is still the case with the lowest vertebrates—the Acrania and Cyclostoma. The same applies to the greater part of the Vermalia or worm-like animals, the various classes and orders of which differ so much in structure. The isolated groups of this rich stem are living branches of a huge tree, the greater part of which has long been dead, and we have no fossil evidence as to its earlier form. Nevertheless, some of the surviving groups are very instructive, and give us clear indications of the way in which the Chordonia were developed from the Vermalia, and these from the Coelenteria.

While we seek the most important of these palingenetic forms among the groups of Coelenteria and Vermalia, it is understood that not a single one of them must be regarded as an unchanged, or even little changed, copy of the extinct stem-form. One group has retained one feature, another a different feature, of the original organisation, and other organs have been further developed and characteristically modified. Hence here, more than in any other part of our genealogical tree, we have to keep before our mind the FULL PICTURE of development, and separate the unessential secondary phenomena from the essential and primary. It will be useful first to point out the chief advances in organisation by which the simple Gastraea gradually became the more developed Chordaea.

We find our first solid datum in the gastrula of the Amphioxus (Figure 1.38). Its bilateral and tri-axial type indicates that the Gastraeads—the common ancestors of all the Metazoa—divided at an early stage into two divergent groups. The uni-axial Gastraea became sessile, and gave rise to two stems, the Sponges and the Cnidaria (the latter all reducible to simple polyps like the hydra). But the tri-axial Gastraea assumed a certain pose or direction of the body on account of its swimming or creeping movement, and in order to sustain this it was a great advantage to share the burden equally between the two halves of the body (right and left). Thus arose the typical bilateral form, which has three axes. The same bilateral type is found in all our artificial means of locomotion—carts, ships, etc.; it is by far the best for the movement of the body in a certain direction and steady position. Hence natural selection early developed this bilateral type in a section of the Gastraeads, and thus produced the stem-forms of all the bilateral animals.

The Gastraea bilateralis, of which we may conceive the bilateral gastrula of the amphioxus to be a palingenetic reproduction, represented the two-sided organism of the earliest Metazoa in its simplest form. The vegetal entoderm that lined their simple gut-cavity served for nutrition; the ciliated ectoderm that formed the external skin attended to locomotion and sensation; finally, the two primitive mesodermic cells, that lay to the right and left at the ventral border of the primitive mouth, were sexual cells, and effected reproduction. In order to understand the further development of the gastraea, we must pay particular attention to: (1) the careful study of the embryonic stages of the amphioxus that lie between the gastrula and the chordula; (2) the morphological study of the simplest Platodes (Platodaria and Turbellaria) and several groups of unarticulated Vermalia (Gastrotricha, Nemertina, Enteropneusta).

We have to consider the Platodes first, because they are on the border between the two principal groups of the Metazoa, the Coelenteria and the Coelomaria. With the former they share the lack of body-cavity, anus, and vascular system; with the latter they have in common the bilateral type, the possession of a pair of nephridia or renal canals, and the formation of a vertical brain or cerebral ganglion. It is now usual to distinguish four classes of Platodes: the two free-living classes of the primitive worms (Platodaria) and the coiled-worms (Turbellaria), and the two parasitic classes of the suctorial worms (Trematoda) and the tape-worms (Cestoda). We have only to consider the first two of these classes; the other two are parasites, and have descended from the former by adaptation to parasitic habits and consequent degeneration.

(FIGURE 2.239. Aphanostomum Langii (Haeckel), a primitive worm of the platodaria class, of the order of Cryptocoela or Acoela. This new species of the genus Aphanostomum, named after Professor Arnold Lang of Zurich, was found in September, 1899, at Ajaccio in Corsica (creeping between fucoidea). It is one-twelfth of an inch long, one-twenty-fifth of an inch broad, and violet in colour. a mouth, g auditory vesicle, e ectoderm, i entoderm, o ovaries, a spermaries, f female aperture, m male aperture.)

The primitive worms (Platodaria) are very small flat worms of simple construction, but of great morphological and phylogenetic interest. They have been hitherto, as a rule, regarded as a special order of the Turbellaria, and associated with the Rhabdocoela; but they differ considerably from these and all the other Platodes (flat worms) in the absence of renal canals and a special central nervous system; the structure of their tissue is also simpler than in the other Platodes. Most of the Platodes of this group (Aphanostomum, Amphichoerus, Convoluta, Schizoprora, etc.) are very soft and delicate animals, swimming about in the sea by means of a ciliary coat, and very small (1/10 to 1/20 inch long). Their oval body, without appendages, is sometimes spindle-shaped or cylindrical, sometimes flat and leaf-shaped. Their skin is merely a layer of ciliated ectodermic cells. Under this is a soft medullary substance, which consists of entodermic cells with vacuoles. The food passes through the mouth directly into this digestive medullary substance, in which we do not generally see any permanent gut-cavity (it may have entirely collapsed); hence these primitive Platodes have been called Acoela (without gut-cavity or coelom), or, more correctly, Cryptocoela, or Pseudocoela. The sexual organs of these hermaphroditic Platodaria are very simple—two pairs of strings of cells, the inner of which (the ovaries, Figure 2.239 o) produce ova, and the outer (the spermaria, s) sperm-cells. These gonads are not yet independent sexual glands, but sexually differentiated cell-groups in the medullary substance, or, in other words, parts of the gut-wall. Their products, the sex-cells, are conveyed out behind by two pairs of short canals; the male opening (m) lies just behind the female (f). Most of the Platodaria have not the muscular pharynx, which is very advanced in the Turbellaria and Trematoda. On the other hand, they have, as a rule, before or behind the mouth, a bulbous sense-organ (auditory vesicle or organ of equilibrium, g), and many of them have also a couple of simple optic spots. The cell-pit of the ectoderm that lies underneath is rather thick, and represents the first rudiment of a neural ganglion (vertical brain or acroganglion).

The Turbellaria, with which the similar Platodaria were formerly classed, differ materially from them in the more advanced structure of their organs, and especially in having a central nervous system (vertical brain) and excretory renal canals (nephridia); both originate from the ectoderm. But between the two germinal layers a mesoderm is developed, a soft mass of connective tissue, in which the organs are embedded. The Turbellaria are still represented by a number of different forms, in both fresh and seawater. The oldest of these are the very rudimentary and tiny forms that are known as Rhabdocoela on account of the simple construction of their gut; they are, as a rule, less than a quarter of an inch long and of a simple oval or lancet shape (Figure 2.240). The surface is covered with ciliated epithelium, a stratum of ectodermic cells. The digestive gut is still the simple primitive gut of the gastraea (d), with a single aperture that is both mouth and anus (m). There is, however, an invagination of the ectoderm at the mouth, which has given rise to a muscular pharynx (sd). It is noteworthy that the mouth of the Turbellaria (like the primitive mouth of the Gastraea) may, in this class, change its position considerably in the middle line of the ventral surface; sometimes it lies behind (Opisthostomum), sometimes in the middle (Mesostomum), sometimes in front (Prosostomum). This displacement of the mouth from front to rear is very interesting, because it corresponds to a phylogenetic displacement of the mouth. This probably occurred in the Platode ancestors of most (or all?) of the Coelomaria; in these the permanent mouth (metastoma) lies at the fore end (oral pole), whereas the primitive mouth (prostoma) lay at the hind end of the bilateral body.

In most of the Turbellaria there is a narrow cavity, containing a number of secondary organs, between the two primary germinal layers, the outer or animal layer of which forms the epidermis and the inner vegetal layer the visceral epithelium. The earliest of these organs are the sexual organs; they are very variously constructed in the Platode-class; in the simplest case there are merely two pairs of gonads or sexual glands—a pair of testicles (Figure 2.241 h) and a pair of ovaries (e). They open externally, sometimes by a common aperture (Monogonopora), sometimes by separate ones, the female behind the male (Digonopora, Figure 2.241). The sexual glands develop originally from the two promesoblasts or primitive mesodermic cells (Figure 1.83 p). As these earliest mesodermic structures extended, and became spacious sexual pouches in the later descendants of the Platodes, probably the two coelom-pouches were formed from them, the first trace of the real body-cavity of the higher Metazoa (Enterocoela).

The gonads are among the oldest organs, the few other organs that we find in the Platodes between the gut-wall and body-wall being later evolutionary products. One of the oldest and most important of these are the kidneys or nephridia, which remove unusable matter from the body (Figure 2.240 nc). These urinary or excretory organs were originally enlarged skin-glands—a couple of canals that run the length of the body, and have a separate or common external aperture (nm). They often have a number of branches. These special excretory organs are not found in the other Coelenteria (Gastraeads, Sponges, Cnidaria) or the Cryptocoela. They are first met in the Turbellaria, and have been transmitted direct from these to the Vermalia, and from these to the higher stems.

Finally, there is a very important new organ in the Turbellaria, which we do not find in the Cryptocoela (Figure 2.239) and their gastraead ancestors—the rudimentary nervous system. It consists of a couple of simple cerebral ganglia (Figure 2.241 g) and fine nervous fibres that radiate from them; these are partly voluntary nerves (or motor fibres) that go to the thin muscular layer developing under the skin; and partly sensory nerves that proceed to the sense-cells of the ciliated epiderm (f). Many of the Turbellaria have also special sense-organs; a couple of ciliated smell pits (na), rudimentary eyes (au), and, less frequently, auditory vesicles.

On these principles I assume that the oldest and simplest Turbellaria arose from Platodaria, and these directly from bilateral Gastraeads. The chief advances were the formation of gonads and nephridia, and of the rudimentary brain. On this hypothesis, which I advanced in 1872 in the first sketch of the gastraea-theory (Monograph on the Sponges), there is no direct affinity between the Platodes and the Cnidaria.

(FIGURE 2.240.