The Evolution of Man, vol 2 by Ernst Haeckel (the top 100 crime novels of all time TXT) 📖

Kelvin (then Sir W. Thomson), attempted to dispense with the hypothesis of spontaneous generation by assuming that the organic inhabitants of the earth were developed from germs that came from the inhabitants of other planets, and that chanced to fall on our planet on fragments of their original home, or meteorites. This hypothesis found many supporters, among others the distinguished German physicist, Helmholtz. However, it was refuted in 1872 by the able physicist, Friedrich Zollner, of Leipzig, in his work, On the Nature of Comets. He showed clearly how unscientific this hypothesis is; firstly in point of logic, and secondly in point of scientific content. At the same time he pointed out that our hypothesis of spontaneous generation is “a necessary condition for understanding nature according to the law of causality.”

I repeat that we must call in the aid of the hypothesis only as regards the Monera, the structureless “organisms without organs.” Every complex organism must have been evolved from some lower organism. We must not assume the spontaneous generation of even the simplest cell, for this itself consists of at least two parts—the internal, firm nuclear substance, and the external, softer cellular substance or the protoplasm of the cell-body. These two parts must have been formed by differentiation from the indifferent plasson of a moneron, or a cytode. For this reason the natural history of the Monera is of great interest; here alone can we find the means to overcome the chief difficulties of the problem of spontaneous generation. The actual living Monera are specimens of such organless or structureless organisms, as they must have boon formed by spontaneous generation at the commencement of the history of life.

 

CHAPTER 2.19. OUR PROTIST ANCESTORS.

Under the guidance of the biogenetic law, and on the basis of the evidence we have obtained, we now turn to the interesting task of determining the series of man’s animal ancestors. Phylogeny us a whole is an inductive science. From the totality of the biological processes in the life of plants, animals, and man we have gathered a confident inductive idea that the whole organic population of our planet has been moulded on a harmonious law of evolution. All the interesting phenomena that we meet in ontogeny and paleontology, comparative anatomy and dysteleology, the distribution and habits of organisms—all the important general laws that we abstract from the phenomena of these sciences, and combine in harmonious unity—are the broad bases of our great biological induction.

But when we come to the application of this law, and seek to determine with its aid the origin of the various species of organisms, we are compelled to frame hypotheses that have essentially a DEDUCTIVE character, and are inferences from the general law to particular cases. But these special deductions are just as much justified and necessitated by the rigorous laws of logic as the inductive conclusions on which the whole theory of evolution is built. The doctrine of the animal ancestry of the human race is a special deduction of this kind, and follows with logical necessity from the general inductive law of evolution.

I must point out at once, however, that the certainty of these evolutionary hypotheses, which rest on clear special deductions, is not always equally strong. Some of these inferences are now beyond question; in the case of others it depends on the knowledge and the competence of the inquirer what degree of certainty he attributes to them. In any case, we must distinguish between the ABSOLUTE certainty of the general (inductive) theory of descent and the RELATIVE certainty of special (deductive) evolutionary hypotheses. We can never determine the whole ancestral series of an organism with the same confidence with which we hold the general theory of evolution as the sole scientific explanation of organic modifications. The special indication of stem-forms in detail will always be more or less incomplete and hypothetical. This is quite natural. The evidence on which we build is imperfect, and always will be imperfect; just as in comparative philology.

The first of our documents, paleontology, is exceedingly incomplete. We know that all the fossils yet discovered are only an insignificant fraction of the plants and animals that have lived on our planet. For every single species that has been preserved for us in the rocks there are probably hundreds, perhaps thousands, of extinct species that have left no trace behind them. This extreme and very unfortunate incompleteness of the paleontological evidence, which cannot be pointed out too often, is easily explained. It is absolutely inevitable in the circumstances of the fossilisation of organisms. It is also due in part to the incompleteness of our knowledge in this branch. It must be borne in mind that the great majority of the stratified rocks that compose the crust of the earth have not yet been opened. We have only a few specimens of the innumerable fossils that are buried in the vast mountain ranges of Asia and Africa. Only a part of Europe and North America has been investigated carefully. The whole of the fossils known to us certainly do not amount to a hundredth part of the remains that are really buried in the crust of the earth. We may, therefore, look forward to a rich harvest in the future as regards this science. However, our paleontological evidence will (for reasons that I have fully explained in the sixteenth chapter of the History of Creation) always be defective.

The second chief source of evidence, ontogeny, is not less incomplete. It is the most important source of all for special phylogeny; but it has great defects, and often fails us. We must, above all, clearly distinguish between palingenetic and cenogenetic phenomena. We must never forget that the laws of curtailed and disturbed heredity often make the original course of development almost unrecognisable. The recapitulation of phylogeny by ontogeny is only fairly complete in a few cases, and is never wholly complete. As a rule, it is precisely the earliest and most important embryonic stages that suffer most from alteration and condensation. The earlier embryonic forms have had to adapt themselves to new circumstances, and so have been modified. The struggle for existence has had just as profound an influence on the freely moving and still immature young forms as on the adult forms. Hence in the embryology of the higher animals, especially, palingenesis is much restricted by cenogenesis; it is to-day, as a rule, only a faded and much altered picture of the original evolution of the animal’s ancestors. We can only draw conclusions from the embryonic forms to the stem-history with the greatest caution and discrimination. Moreover, the embryonic development itself has only been fully studied in a few species.

Finally, the third and most valuable source of evidence, comparative anatomy, is also, unfortunately, very imperfect; for the simple reason that the whole of the living species of animals are a mere fraction of the vast population that has dwelt on our planet since the beginning of life. We may confidently put the total number of these at more than a million species. The number of animals whose organisation has been studied up to the present in comparative anatomy is proportionately very small. Here, again, future research will yield incalculable treasures. But, for the present, in view of this patent incompleteness of our chief sources of evidence, we must naturally be careful not to lay too much stress in human phylogeny on the particular animals we have studied, or regard all the various stages of development with equal confidence as stem-forms.

In my first efforts to construct the series of man’s ancestors I drew up a list of, at first ten, afterwards twenty to thirty, forms that may be regarded more or less certainly as animal ancestors of the human race, or as stages that in a sense mark off the chief sections in the long story of evolution from the unicellular organism to man. Of these twenty to thirty stages, ten to twelve belong to the older group of the Invertebrates and eighteen to twenty to the younger division of the Vertebrates.

In approaching, now, the difficult task of establishing the evolutionary succession of these thirty ancestors of humanity since the beginning of life, and in venturing to lift the veil that covers the earliest secrets of the earth’s history, we must undoubtedly look for the first living things among the wonderful organisms that we call the Monera; they are the simplest organisms known to us—in fact, the simplest we can conceive. Their whole body consists merely of a simple particle or globule of structureless plasm or plasson. The discoveries of the last four decades have led us to believe with increasing certainty that wherever a natural body exhibits the vital processes of nutrition, reproduction, voluntary movement, and sensation, we have the action of a nitrogenous carbon-compound of the chemical group of the albuminoids; this plasm (or protoplasm) is the material basis of all vital functions. Whether we regarded the function, in the monistic sense, as the direct action of the material substratum, or whether we take matter and force to be distinct things in the dualistic sense, it is certain that we have not as yet found any living organism in which the exercise of the vital functions is not inseparably bound up with plasm.

The soft slimy plasson of the body of the moneron is generally called “protoplasm,” and identified with the cellular matter of the ordinary plant and animal cells. But we must, to be accurate, distinguish between the plasson of the cytodes and the protoplasm of the cells. This distinction is of the utmost importance for the purposes of evolution. As I have often said, we must recognise two different stages of development in these “elementary organisms,” or plastids (“builders”), that represent the ultimate units of organic individuality. The earlier and lower stage are the unnucleated cytodes, the body of which consists of only one kind of albuminous matter—the homogeneous plasson or “formative matter.” The later and higher stage are the nucleated cells, in which we find a differentiation of the original plasson into two different formative substances—the caryoplasm of the nucleus and the cytoplasm of the body of the cell (cf. Chapter 1.6.)

(FIGURE 2.226. Chroococcus minor (Nageli), magnified 1500 times. A phytomoneron, the globular plastids of which secrete a gelatinous structureless membrane. The unnucleated globule of plasm (bluish-green in colour) increases by simple cleavage (a to d).

The Monera are permanent cytodes. Their whole body consists of soft, structureless plasson. However carefully we examine it with our finest chemical reagents and most powerful microscopes, we can find no definite parts or no anatomic structure in it. Hence, the Monera are literally organisms without organs; in fact, from the philosophic point of view they are not organisms at all, since they have no organs. They can only be called organisms in the sense that they are capable of the vital functions of nutrition, reproduction, sensation, and movement. If we were to try to imagine the simplest possible organism, we should frame something like the moneron.

The Monera that we find to-day in various forms fall into two groups according to the nature of their nutrition—the Phytomonera and the Zoomonera; from the physiological point of view, the former are the simplest specimens of the plant (phyton) kingdom, and the latter of the animal (zoon) world. The Phytomonera, especially in their simplest form, the Chromacea (Phycochromacea or Cyanophycea), are the most primitive and the oldest of living organisms. The typical genus Chroococcus (Figure 2.226) is represented by several freshwater species, and often forms a very delicate bluish-green deposit on stones and wood in ponds and ditches. It consists of round, light green particles, from 1/7000 to 1/2500 of an inch in diameter.

(FIGURE 2.227. Aphanocapsa primordialis (Nageli), magnified 1000 times. A phytomoneron, the round plastids of which (bluish-green in colour) secrete a shapeless gelatinous mass; in this the unnucleated cytodes increase continually by simple cleavage.)