CHAPTER VIII THE ORGANIC AND THE INORGANIC
It is convenient that we should express the results of biological investigation in schemes of classification, for only in this way can we reduce the apparent chaos of naturally occurring organic things to order, and state our knowledge in such a way that it can easily be communicated to others. But we must always remember that the classifications of systematic biology are conceptual arrangements, depending for their precise nature on the point of view taken by their authors. The clear-cut distinctions that apparently separate phylum from phylum, class from class, order from order, and so on, do not really exist. There are no such categories of organisms in nature as genera, families, and the higher groupings. All that we can say exist naturally are the species, since all the organisms composing each of these groups are related together by ties of blood-relationship, and all are isolated from the organisms composing other species by physiological dissimilarities which render the plants or animals of one species infertile with those of any other. Such would doubtless have been the opinion of most botanists and zoologists prior to the work of de Vries, but we must now recognise that the systematic, or Linnean, species of the nineteenth century was just as artificial a category as were the genera and families. Our arrangements of plants and animals into systematic species and the higher groupings are therefore convenient ways of symbolising the results of morphological and physiological investigations, although they also indicate the main directions taken by the evolutionary process, but the manner in which they are stated in taxonomic schemes is always a more or less formal one.
There are no absolute distinctions between group and group, even between the animals and the plants. There is nothing, for instance, in the morphology of a Diatom to indicate that it belongs to the vegetable kingdom, or in that of a Radiolarian, to indicate that it is an animal. Peridinians are either plants or animals according to the general argument, or the point of view of the author who writes about them. Even a study of the energy-transformations that are effected in the living substance of these lower organisms does not afford an absolute distinction: synthetic metabolic processes in which energy passes into the potential condition may be carried out in animals, while many plants—the saprophytic fungi, or the insectivorous plants, for instances—may effect analytic energy-transformations of essentially the same nature as those exhibited in the typical mode of animal metabolism. Motility and the possession of a sensori-motor system do not afford the means of making a sharply drawn line of division between plants and animals. Potential energy passes into the condition of kinetic energy in the typical animal, and this kinetic energy is directed by the sensori-motor system. But some lower unicellular plants are motile, and they possess the rudiments of a sensori-motor system in the flagella by which their movements are effected. On the other hand, the sensori-motor system has become vestigial in many animal parasites—in the Crustacean Sacculina, for instance, which is parasitic on some Crabs. The possession of consciousness, in so far as we can say that other animals than ourselves possess it, is no distinction between the two kingdoms of life. Consciousness, judged by the degree of development of motility, must be supposed to be absent or very dim in the extreme cases of parasitism attained by some animals; on the other hand, we may assume that it is present, to some extent at least, in the highly motile zoospores of the Algæ. Thus some lower organisms, the Peridinians and the algal spores, exhibit all the characters which we utilise in separating animals from plants—the chlorophyllian apparatus, by means of which the kinetic energy of solar radiation becomes transformed into the potential energy of organic chemical compounds; the apparatus of receptor and motile organs, by means of which the potential energy of stored chemical compounds passes into the kinetic energy of bodily movements; and the existence (so far as we can say that it exists in organisms other than ourselves) of some degree of consciousness.
Neither do those morphological schemata which we construct as diagnostic of phyla, or classes, or orders, etc., separate these groups from each other so clearly and unequivocally as our classifications suggest. It might seem for instance that the presence or absence of a notochord would sharply distinguish between the vertebrate and invertebrate, but structures which suggest in their development the true notochordal skeleton of the typical vertebrate animal are to be traced in animals which exhibit few or none of the characters which we regard as diagnostic of the Vertebrate. Typical Arthropods and typical Vertebrates seem to be distinct from each other, but the extinct Ostracoderms of Silurian times may have been animals which possessed an internal axial skeleton, and which were also armed by a heavy dermal exo-skeleton. It is a hypothesis of considerable plausibility that they really were Arthropods, on the other hand they are usually regarded as Vertebrates. So also with most other phyla: the morphological characters which absolutely distinguish between one group and others are very few indeed, and the small appended groups that lie about the bases of these larger groups may present one or other of the characters of several phyla. Looking at the morphology of the animal kingdom in a general kind of way, one does indeed see that a certain structural plan is characteristic of the organisms belonging to each of the great phyla, while more detailed structural plans may be said to be characteristic of the sub-groups. But minute morphological and embryological investigation reduces almost to nothing the characters which are absolutely diagnostic of these various groups.
No more than the nature of the energy-transformations, and the essential morphology, does the behaviour of animals afford us the means of setting up absolute distinctions between group and group. Really tropistic behaviour is exhibited by the movements of the stems, roots, and leaves of green plants, or in the movements of Bacteria, and perhaps some unicellular animals. Typically instinctive behaviour is exhibited by the individuals of societies of Insects and by many solitary-living animals belonging to this class; and typically intelligent behaviour is exhibited by the acting of the higher Mammalia. Yet there is undoubtedly much that is truly instinctive in the behaviour of Man, and something of the same nature as his intelligence seems to inhere in the instinctively-acting mammal or insect: how else could an instinctive action become capable of improvement? We cannot doubt that intelligence is manifested by a dog or by much that we see in the behaviour of ants. No rigid distinctions between tropisms, such as we have mentioned above, and the reflexes that may be taken to constitute instinctive behaviour, can be established. Minute analysis, such as that carried out by Jennings on the swimming movements of the Protozoa, leaves us quite in doubt as to how these modes of behaviour are most properly to be described; and all the controversy as to the nature of tropisms, reflexes, instinct, and intelligence surely indicates that these modes of behaviour have something that is common to all of them, and that no clear and certain distinction can be said to separate one from the other. Even those psychic processes which we call intellectual do not seem to be different in kind from some that we attribute to the lower animals: the Protozoan Paramœcium studied by Jennings, or the crabs, crayfishes, and starfishes studied by Yerkes and others really learn to perform actions, but this learning is said to be the result of a process of “trial and error.” The animal tries one series of movements and finds that it fails, tries another and another with a similar result, and in the end finds one that is effective. This is remembered, and when the same problem again confronts the animal it is solved after fewer trials, and finally, after experience, the end-result is attained at once without previous trials. Now many of what we call truly intellectual processes are certainly processes of precisely this nature. Hypothesis after hypothesis occurs to the scientific man (or to the detective, or to the engineer confronted with some exceptional difficulty), and one after another is tested by actual trial, or by a process of reasoning (which is really the rapid and formal resuming of previous experience), until a hypothesis verifiable, or a priori verifiable, is found. What, for instance, are our mathematical methods of integrating a function, or working a long division sum, but methods of scientific “guessing,” and verification of the hypotheses so made? They are truly instances of the method of trial and error practised by the lower animals.
All the above amounts to saying that there is a community of energetic processes, of morphology, and of behaviour in animals and plants. “Protoplasm” is the same, or much the same chemical aggregate, whether it is contained in the cells of animals or plants. The cell, with its nucleus, chromatic architecture, cell-inclusions, and cell-wall, is essentially the same structure in all organisms. The complex and specialised process of nuclear division in tissue growth, or the series of events which constitute the acts of fertilisation of the ovum or its plant correlative, are the same all through the organic world. The sensori-motor system—receptor organ, nerve-fibre and cell, and effector-motor organ—is the same all through the animal kingdom. Alimentary canal and glands, enzymes, excretory tubules, contractile blood-vascular apparatus—all these are structures which are functionally the same, which are built on essentially the same morphological plan. Life, whether it is the life of plant or animal, makes use of the same material means of perpetuating itself on the earth and avoiding the descent of matter towards complete inertia.
Absolute dissimilarities, dissimilarities such as those between atoms of hydrogen and oxygen, or between a point and a straight line, or between rest and motion, do not exist between the different categories of entities that make up the organic world. Yet differences do exist, and must we conclude that because these differences are not absolute ones, because they are differences of degree, and not of kind, they are not essential, are not differences at all? Must we say, for instance, that although an animal is a much more efficient machine than a gas-engine (in the sense of efficiency as understood by the engineer), there is really no difference between them, that they are both thermo-dynamic mechanisms, since in both energy is dissipated? Ought we to say that, because the last steps in the formation of urea in the animal body are synthetic ones, there is really no difference between the nature of the energy-transformations that occur in the animal and the plant modes of metabolism? Ought we to say that, because a dog may sometimes act intelligently and a man instinctively, psychically they are similarly-behaving organisms? Surely this amounts to saying that, because things are not absolutely different, they are the same; and surely the mode of reasoning is a vicious one!
What we clearly see in the different kinds of organisms—in the metabolically constructive plant and the metabolically destructive animal; or in the instinctively-acting Arthropod and the intelligently-acting Mammal—is the progressive development of different tendencies. If the green plant is, in its essence, the same kind of physico-chemical constellation as is the animal, yet the tendency of its evolution has been that more and more it has acquired the habit, or the power, of using solar radiation to combine together carbon dioxide, water, and nitrogenous inorganic salts to form proteid and carbohydrate substances. On the other hand, the tendency of the animal has been more and more to absorb into its own tissues the proteid and carbohydrates synthesised by the green plant, and then to break these substances down into carbon dioxide and water, and less and less to effect such syntheses as are effected by the plant. Even if the Annelid worm, the Arthropod, and the Vertebrate were, at the origin of their ancestries, animals which were very like each other in the morphological sense; even if there are some Arthropods which are very like Annelids, and some Annelids which might very easily be imagined to become transformed into Vertebrates, and some extinct Arthropods which may after all have been Vertebrates, yet it is the case that the tendencies of the evolution of each of these groups have been very different. All the while the Vertebrate tended more and more to develop a rigid axial rod or notochord, becoming later a jointed vertebral column, and a soft, pliable, exo-skeleton; while the Arthropod tended more and more to develop a rigid exo-skeleton, and to remain soft in its axial parts. Even if these two tendencies may not have been fully realised, is it not the case that they are really different things? The evolutionary process has therefore been, in its essence, the development, or unfolding, of tendencies originally one.
What is the evolutionary process? It is usually regarded as a progress from organic simplicity towards organic complexity. Yet if we think about it as a physical process we cannot say that any one stage is any more simple or complex than any other stage. Let us compare organic evolution with the process of inorganic evolution, as, of course, we are compelled to do if we regard the former process as a physico-chemical one. Assume, then, that the nebular hypothesis of Kant and Laplace is true—it will make no difference to our argument even if this hypothesis is not true, and it is more easily understood than any other hypothesis of planetary evolution. Originally all the materials composing our solar system existed in the form of a gaseous nebula possessing a slow rotatory motion of its own. It does not matter that the silicates, carbonates, oxides, and all other mineral substances that we now know existed then in the form of chemical elements, or the precursors of chemical elements: all the material bodies now present in the solar system were present in the original nebula. The energy of this nebula consisted of the potential energy represented by the separation of atoms which later on became combined together, and of the kinetic energy of motion of these atoms; and this material and energy, together with the other cosmic bodies radiating energy to it and those bodies receiving the energy which it lost by its own radiation, constituted a system, in the sense of the term as it is employed by the physicists. Now, in the process of cosmic evolution this system became transformed, because it was continually losing energy by radiation. As it cooled, the mean free paths of its atoms and molecules became less and less, and finally condensation to the liquid and then to the solid condition occurred. The parts of the nebula continually gravitated together, so that it became smaller and smaller while its rotatory motion became greater. Finally, mechanical strains became set up in its mass as the consequence of the increased velocity of rotation, and disruption occurred with the formation of the sun, the planets, and the satellites. There was no increase of complexity of the system. At any moment of time its elements, that is, the chemical atoms composing it and the energy of these atoms, was the same as at any other moment of time. Heat-energy may have been radiated from one part of the system—the heated nebula—to some other part of the system—the other cosmic bodies absorbing this radiation, but the total energy of the system remained the same. The chemical atoms may have combined together to form molecules and compounds, and their energy of position may have become the energy of motion, but the ultimate materials were still the same. What happened during the cooling and contraction of the nebula was a rearrangement of the elements of the system, that is, of the atoms and their energies. At any moment of time the condition of the system was an inevitable consequence of the condition at the moment immediately preceding this, and a strict functionality, in the mathematical sense, existed between the two conditions. It was not more complex in the later stage than in the earlier one—it was merely different. Stages of evolution were really phases in a transforming system of matter and energies.