PEDIGREE AND HISTORY OF THE ANIMAL KINGDOM.
I. Animal-Plants and Worms.
The Natural System of the Animal Kingdom.—Linnæus and Lamarck’s Systems.—The Four Types of Bär and Cuvier.—Their Increase to Seven Types.—Genealogical Importance of the Seven Types as Independent Tribes of the Animal Kingdom.—Derivation of Zoophytes and Worms from Primæval Animals.—Monophyletic and Polyphyletic Hypothesis of the Descent of the Animal Kingdom.—Common Origin of the Four Higher Animal Tribes out of the Worm Tribe.—Division of the Seven Animal Tribes into Sixteen Main Classes, and Thirty-eight Classes.—Primæval Animals (Monera, Amœbæ, Synamœbæ), Gregarines, Infusoria, Planæades, and Gastræades (Planula and Gastrula).—Tribe of Zoophytes.—Spongiæ (Mucous Sponges, Fibrous Sponges, Calcareous Sponges).—Sea Nettles, or Acalephæ Corals, Hood-jellies, Comb-jellies).—Tribe of Worms.
The natural system of organisms which we must employ in the animal as well as in the vegetable kingdom, as a guide in our genealogical investigations, is in both cases of but recent origin, and essentially determined by the progress of comparative anatomy and ontogeny (the history of individual development) during the present century. Almost all the attempts at classification made in the last century followed the path of the artificial system, which was first established in a consistent manner by Charles Linnæus. The artificial system differs essentially from the natural one, in the fact that it does not make the whole organization and the internal structure (depending upon the blood relationship) the basis of classification, but only employs individual, and for the most part external, characteristics, which readily strike the eye. Thus Linnæus distinguished his twenty-four classes of the vegetable kingdom principally by the number, formation, and combination of the stamens. In like manner he distinguished six classes in the animal kingdom principally by the nature of the heart and blood. These six classes were: (1) Mammals; (2) Birds; (3) Amphibious Animals; (4) Fishes; (5) Insects; and (6) Worms.
But these six animal classes of Linnæus are by no means of equal value, and it was an important advance when, at the end of the last century, Lamarck comprised the first four classes as vertebrate animals (Vertebrata), and put them in contrast with the remaining animals (the insects and worms of Linnæus), of which he made a second main division—the invertebrate animals (Invertebrata). In reality Lamarck thus agreed with Aristotle, the father of Natural History, who had distinguished these two main groups, and called the former blood-bearing animals, the latter bloodless animals.
The next important progress towards a natural system of the animal kingdom was made some decades later by two most illustrious zoologists, Carl Ernst Bär and George Cuvier. As has already been remarked, they established, almost simultaneously and independently of one another, the proposition that it was necessary to distinguish several completely distinct main groups in the animal kingdom, each of which possessed an entirely peculiar type or structure (compare above, vol. i. p. [53]). In each of these main divisions there is a tree-shaped and branching gradation from most simple and imperfect forms to those which are exceedingly composite and highly developed. The degree of development within each type is quite independent of the peculiar plan of structure, which forms the basis of the type and gives it a special characteristic. The “type” is determined by the peculiar relations in position of the most important parts of the body, and the manner in which the organs are connected. The degree of development, however, is dependent upon the greater or less division of labour among organs, and on the differentiation of the plastids and organs. This extremely important and fruitful idea was established by Bär, who relied more distinctly and thoroughly upon the history of individual development than did Cuvier. Cuvier based his argument upon the results of comparative anatomy. But neither of them recognized the true cause of the remarkable relationships pointed out by them, which is first revealed to us by the Theory of Descent. It shows us that the common type or plan of structure is determined by inheritance, and the degree of development or differentiation by adaptation. (Gen. Morph. ii. 10).
Both Bär and Cuvier distinguished four different types in the animal kingdom, and divided it accordingly into four great main divisions (branches or circles). The first of these is formed by the vertebrate animals (Vertebrata), and comprises Linnæus’ first four classes—mammals, birds, amphibious animals, and fishes. The second type is formed by the articulated animals (Articulata), containing Linnæus’ insects, consequently the six-legged insects, and also the myriopods, spiders, and crustacea, but besides these, a large number of the worms, especially the ringed worms. The third main division comprises the molluscous animals (Mollusca)—slugs, snails, mussels, and some kindred groups. Finally, the fourth and last circle of the animal kingdom comprises the various radiated animals (Radiata), which at first sight differ from the three preceding types by their radiated, flower-like form of body. For while the bodies of molluscs, articulated animals, and vertebrated animals consist of two symmetrical lateral halves—of two counterparts or antimera, of which the one is the mirror of the other—the bodies of the so-called radiated animals are composed of more than two, generally of four, five, or six counterparts grouped round a common central axis, as in the case of a flower. However striking this difference may seem at first, it is, in reality, a very subordinate one, and the radial form has by no means the same importance in all “radiated animals.”
The establishment of these natural main groups or types of the animal kingdom by Bär and Cuvier was the greatest advance in the classification of animals since the time of Linnæus. The three groups of vertebrated animals, articulated animals, and molluscs are so much in accordance with nature that they are retained, even at the present day, little altered in extent. But a more accurate knowledge soon showed the utterly unnatural character of the group of the radiated animals. Leuckart, in 1848, first pointed out that two perfectly distinct types were confounded under the name, namely, the Star-fishes (Echinoderma)—the sea-stars, lily encrinites, sea-urchins, and sea-cucumbers; and, on the other hand, the Animal-plants, or Zoophytes (Cœlenterata or Zoophyta)—the sponges, corals, hood-jellies, and comb-jellies. At the same time, Siebold united the Infusoria with the Rhizopoda, under the name of Protozoa (lowest animals), into a special main division of the animal kingdom. By this the number of animal types was increased to six. It was finally increased to seven by the fact that modern zoologists separated the main division of the articulated animals into two groups: (a) those possessing articulated feet (Arthropoda), corresponding to Linnæus’ Insects, namely, the Flies (with six legs), Myriopods, Spiders, and Crustacea; and (b) the footless Worms (Vermes), or those possessing non-articulated feet. These latter comprise only the real or genuine Worms (ring-worms, round worms, planarian worms, etc.), and therefore in no way correspond with the Worms of Linnæus, who had included the molluscs, the radiates, and many other lower animals under this name.
Thus, according to the views of modern zoologists, which are given in all recent manuals and treatises on zoology, the animal kingdom is composed of seven completely distinct main divisions or types, each of which is distinguished by a characteristic plan of structure peculiar to it, and perfectly distinct from every one of the others. In the natural system of the animal kingdom—which I shall now proceed to explain as its probable pedigree—I shall on the whole agree with this usual division, but not without some modifications, which I consider very important in connection with genealogy, and which are rendered absolutely necessary in consequence of our view as to the history of the development of animals.
We evidently obtain the greatest amount of information concerning the pedigree of the animal kingdom (as well as concerning that of the vegetable kingdom) from comparative anatomy and ontogeny. Besides these, palæontology also throws much valuable light upon the historical succession of many of the groups. From numerous facts in comparative anatomy, we may, in the first place, infer the common origin of all those animals which belong to one of the seven “types.” For in spite of all the variety in the external form developed within each of these types, the essential relative position of the parts of the body which determines the type, is so constant, and agrees so completely in all the members of every type, that on account of their relations of form alone we are obliged to unite them, in the natural system, into a single main group. But we must certainly conclude, moreover, that this conjunction also has its expression in the pedigree of the animal kingdom. For the true cause of the intimate agreement in structure can only be the actual blood relationship. Hence we may, without further discussion, lay down the important proposition that all animals belonging to one and the same circle or type must be descended from one and the same original primary form. In other words, the idea of the circle or type, as it is employed in zoology since Bär and Cuvier’s time to designate the few principal main groups or “sub-kingdoms” of the animal kingdoms, coincides with the idea of “tribe” or “phylum,” as employed by the Theory of Descent.
If, then, we can trace all the varieties of animal forms to these seven fundamental forms, the following question next presents itself to us as a second phylogenetic problem—Where do these seven animal tribes come from? Are they seven original primary forms of an entirely independent origin, or are they also distantly related by blood to one another?
| Haeckel-History of Creation | Pl. VI. |
At first we might be inclined to answer this question in a polyphyletic sense, by saying that we must assume, for each of the seven great animal tribes, at least one independent primary form completely distinct from the others. On further considering this difficult problem, we arrive in the end at the notion of a monophyletic origin of the animal kingdom, viz., that these seven primary forms are connected at their lowest roots, and that they are derived from a single, common primæval form. In the animal as well as in the vegetable kingdom, when closely and accurately considered, the monophyletic hypothesis of descent is found to be more satisfactory than the polyphyletic hypothesis.
It is comparative ontogeny (embryology) which first and foremost leads to the assumption of the monophyletic origin of the whole animal kingdom (the Protista excepted of course). The zoologist who has thoughtfully compared the history of the individual development of various animals, and has understood the importance of the biogenetic principle (p. [33]), cannot but be convinced that a common root must be assumed for the seven different animal tribes, and that all animals, including man, are derived from a single, common primary form. The result of the consideration of the facts of embryology, or ontogeny, is the following genealogical or phylogenetic hypothesis, which I have put forward and explained in detail in my “Philosophy of Calcareous Sponges” (Monograph of the Calcareous Sponges, vol. i. pp. 464, 465, etc.,—“the Theory of the Layers of the Embryo, and the Pedigree of Animals.”)
The first stage of organic life in the Animal kingdom (as in the Vegetable and Protista kingdoms) was formed by perfectly simple Monera, originating by spontaneous generation. The former existence of this simplest animal form is, even at present, attested by the fact that the egg-cell of many animals loses its kernel directly after becoming fructified, and thus relapses to the lower stage of development of a cytod without a kernel, like a Moneron. This remarkable occurrence I have interpreted, according to the law of latent inheritance (vol. i. p. [205]), as a phylogenetic relapse of the cellular form into the original form of a cytod. The Monerula, as we may call this egg-cytod without a kernel, repeats then, according to the biogenetic principle (vol. ii. p. [33]), the most ancient of all animal forms, the common primary form of the animal kingdom, namely, the Moneron.
The second ontogenetic process consists in a new kernel being formed in the Monerula, or egg-cytod, which thus returns again to the value of a true egg-cell. According to this, we must look upon the simple animal cell, containing a kernel, or the single-celled primæval animal—which may still be seen in a living state in the Amœbæ of the present day—as the second step in the series of phylogenetic forms of the animal kingdom. Like the still living simple Amœbæ, and like the naked egg-cells of many lower animals (for example, of Sponges and Medusæ, etc.), which cannot be distinguished from them, the remote phyletic primary Amœbæ also were perfectly simple naked-cells, which moved about in the Laurentian primæval ocean, creeping by means of the ever-changing processes of their body-substance, and nourishing and propagating themselves in the same way as the Amœbæ of the present day. (Compare vol. i. p. [188], and vol. ii. p. [54.]) The existence of this Amœba-like, single-celled primary form of the whole animal kingdom is unmistakably indicated by the exceedingly important fact that the egg of all animals, from those of sponges and worms up to those of the ant and man, is a simple cell.
Thirdly, from the “single-cell” state arose the simplest multicellular state, namely, a heap or a small community of simple, equiformal, and equivalent cells. Even at the present day, in the ontogenetic development of every animal egg-cell, there first arises a globular heap of equiformal naked cells, by the repeated self-division of the primary cell. (Compare vol. i. p. [190] and the [Frontispiece], [Fig. 3].) We called this accumulation of cells the mulberry state (Morula), because it resembles a mulberry or blackberry. This Morula-body occurs in the same simple form in all the different tribes of animals, and on account of this most important circumstance we may infer—according to the biogenetic principle—that the most ancient, many-celled, primary form of the animal kingdom resembled a Morula like this, and was in fact a simple heap of Amœba-like primæval cells, one similar to the other. We shall call this most ancient community of Amœbæ—this most simple accumulation of animal cells—which is recapitulated in individual development by the Morula—the Synamœba.
Out of the Synamœbæ, in the early Laurentian period, there afterwards developed a fourth primary form of the animal kingdom, which we shall call the ciliated germ (Planæa). This arose out of the Synamœba by the outer cells on the surface of the cellular community beginning to extend vibrating fringes called cilia, and becoming “ciliated cells,” and thus differentiating from the inner and unchanged cells. The Synamœbæ consisted of completely equi-formed and naked cells, and crept about slowly, at the bottom of the Laurentian primæval ocean, by means of movements like those of an Amœba. The Planæa, on the other hand, consisted of two kinds of different cells—inner ones like the Amœbæ, and external “ciliated cells.” By the vibrating movements of the cilia the entire multicellular body acquired a more rapid and stronger motion, and passed over from the creeping to the swimming mode of locomotion. In exactly the same manner the Morula, in the ontogenesis of lower animals, still changes into a ciliated form of larva, which has been known, since the year 1847, under the name of Planula. This Planula is sometimes a globular, sometimes an oval body, which swims about in the water by means of a vibrating movement; the fringed (ciliated) and smaller cells of the surface differ from the larger inner cells, which are unfringed. (Fig. 4 of the Frontispiece.)
Out of this Planula, or fringed larva, there then develops, in animals of all tribes, an exceedingly important and interesting animal form, which, in my Monograph of the Calcareous Sponges, I have named Gastrula (that is, larva with a stomach or intestine). (Frontispiece, Fig. 5, 6). This Gastrula externally resembles the Planula, but differs essentially from it in the fact that it encloses a cavity which opens to the outside by a mouth. The cavity is the “primary intestine,” or “primary stomach,” the progaster, the first beginning of the alimentary canal; its opening is the “primary mouth” (prostoma). The wall of the progaster consists of two layers of cells: an outer layer of smaller ciliated cells (outer skin, or ectoderm), and of an inner layer of larger non-ciliated cells (inner skin, or entoderm). This exceedingly important larval form, the “Gastrula,” makes its appearance in the ontogenesis of all tribes of animals—in Sponges, Medusæ, Corals, Worms, Sea-squirts, Radiated animals, Molluscs, and even in the lowest Vertebrata (Amphioxus: compare p. 200, Plate [XII]., Fig. B 4; see also in the same place the Ascidian, Fig. A 4).