The brain and cord are a switch-board of unimaginable complexity, so that an efferent impulse entering it from, say, the eye, can be shunted on to one nerve path after another, so that it may affect any muscle in the whole body. This is no fiction: it may actually be the case. In normal respiration a centre in the hind-brain is stimulated to rhythmical activity by the presence of carbon dioxide in the blood, and from it efferent impulses originate which stimulate the muscles of the chest wall and diaphragm. But in the distress of asphyxia every muscle of the body may be stimulated to activity in the effort to accelerate the oxygenation of the blood, and these are not spasmodic movements of the muscles of limbs, etc., but purposeful contractions having for their object the increased intake of air into the lungs. The central nervous system is, therefore, a switch-board—so mechanistic physiology teaches, neglecting any idea of an operator. But the whole trend of modern investigation is to show that every increase of specialisation in the evolution of the higher animal adds to the complexity of this nervous apparatus by increasing the number of alternative paths that an impulse originating anywhere in the body may take before it issues from the brain or spinal cord. Yet with all this increase of complexity it is nevertheless the case that in the higher animal the various parts of the central and peripheral nervous system are more and more integrated, so that in the actions of the animal it becomes more and more the organism as a whole that acts.

All other organs in the animal body—excepting always the reproductive apparatus—are accessory to the sensori-motor system. The alimentary canal and its glands dissolve the food-stuffs ingested; the metabolic organs, that is, the cells of the wall of the intestine, the liver, etc., transform these ingested proteids, fats, and carbohydrates of the food into the proteids, fats, and carbohydrates of the animal itself; the heart, blood, and lymph vessels carry this food material to the muscles and nervous organs; the respiratory organs absorb oxygen which is distributed throughout the body in the blood stream; the excretory organs, that is, the lungs, skin, and kidneys, remove noxious materials like carbonic acid and urea, or its precursors; and purposeful changes of functioning of all these organs are brought about by changes in motor activity. Round the sensori-motor system all the rest of the structure of the animal body is built up.

What we see clearly in the evolution of the animal body is the progressive increase of activity of the sensori-motor system. The animal becomes more and more mobile. It is in this way that dominance has been attained and all the directions of structural evolution in the past that have not tended in this direction have been unsuccessful, irreversible, evolutionary processes. Great size has not succeeded in the animal kingdom, and so the gigantic reptiles and mammals of the secondary and tertiary periods have become extinct. Defence against enemies by the development of dermal armour has not succeeded, and so the Dinosaurs, and other armed animals of the Tertiary Age have also become extinct. The transformation of the fore limbs of the reptile into wings, or the legs of the mammal into flappers, did not succeed, because all the rest of the structure of these animals had become adapted to locomotion on dry land, and the change of structure had become too profound to be modified: so the Pterodactyls passed away, as the whales of our own period are also passing. Only in the lightly boned, feathered bird, with the possibility of the development of powerful pectoral muscles, did indefinite possibilities of flight reside; and only in the fish, with the concomitant evolution of gills, the reduction of a minimum of the mass of the alimentary canal and its glands, and the conversion of most of the muscles of the body into organs actuating the tail fin, was the completeness of adaptation to aquatic life realised. Mobility, a bodily structure capable of indefinitely varied movements, and a nervous system by the aid of which any part of the body might become linked to any other part—these were the structural adaptations that have been successful alike in Arthropod and Vertebrate.

There were apparently two main types of structure by means of which this mobility and elasticity could be attained, the Arthropod type and the Vertebrate type. There seems little to choose between them if we had to select one of them in order to obtain a highly mobile organic mechanism. Arthropod and Vertebrate seem to be equally complex if we take account of difference in size and the additional bodily mechanism that great size must involve. Certainly the musculature of the Vertebrate is more complex than in the Arthropod. But greater weight must require larger and more powerful muscles if the same degree of mobility relative to the size of the animal is to be attained, and this more complex musculature must carry with it a more complex brain. It must also be concomitant with a more massive skeleton, for rigid supports for the muscles must be present in the mechanism. Why are there no great insects or crustaceans? Mr Wells has suggested in one of his novels the formidability of a wasp two feet long! Such a creature would indeed be more dreadful than any predatory bird that we know if its activity were also that of the wasps that we know, just as a Copepod as large as a shark would be a more formidable animal than the fish. It seems possible that the reason for the smaller size of the Vertebrate is to be found in the nature of the skeleton. Powerful muscles would require a very strong and thick carapace, and this would attain a mass in a very large insect or crustacean which would require too much energy for its rapid transport. A rigid exoskeleton like that of an Arthropod also means that growth must take place by a process of ecdysis, that is, the animal grows only during the periods when it casts its shell; and the necessity of this process of ecdysis must be a formidable disadvantage in the case of a very large animal, if indeed it would be possible at all. Thus the Arthropod developing an exoskeleton must remain small, and this smallness, fortunately for the Vertebrate, has made it the less formidable animal. It was an accident of evolution that the Arthropods developed an exoskeleton instead of an endoskeleton.

Undoubtedly the internal skeleton of the Vertebrates, with its light, hollow, cancellated bones, was mechanically the best means for the attachment of muscles. It made possible a greater degree of freedom of movement of the parts of the body, greater variety and plasticity of action, and it removed, to some extent, the limit of size and the embarrassing discontinuity of growth by ecdysis, with all the dangers that this involves. Above all, it led to the increased complexity of the central nervous system, since this became bound up with the increasing variety of bodily movement.

In the evolution of the dominant groups of organisms we see, then, the development of several tendencies. First, that tendency which seems to offer the greatest contrast to the universal tendency displayed in inorganic processes, the dissipation of energy. The plant organism is essentially a system in which energy is accumulated in the potential form. Then, in the animal kingdom we see that the main tendency of evolution has been the development of systems in which energy becomes expended in infinitely varied movements. It may seem, on superficial examination, that in the animal mode of metabolism energy is dissipated as it is in inorganic processes; and this is the conclusion that we should reach if we considered the actions, and the results of the actions, of the lower animals only, that is, animals lower than man. We return to this point later on, but in the meantime it is to be noted that the fundamental division of organisms is that founded upon their activities as energy-transformers, that is, into plants and animals. Within each of these kingdoms of organisms structural evolution has occurred: the unicellular green plant has evolved along very numerous lines, each of them characterised by a different type of morphological structure. The unicellular animal has also evolved in a similar way with the result that the present phyla have become established. Looking at these great groups of animals, we see that two of them have attained dominance by the development along different lines of a sensori-motor system. Here we see another fundamental difference between the plant and animal organism, but one which is a consequence of the difference that exists between the two kingdoms in respect of the energy-transformations carried out by them. The plant is characterised by immobility, the animal by mobility.

Immobility implies unconsciousness, mobility consciousness, and this physical difference is the third one which we can establish between the plant and the animal. Now few physiologists are likely to accept this distinction as one which has any real objective meaning. Consciousness is not a concept to be dealt with in any process of reasoning, it is not even something felt in the way in which we speak of the feelings of pain, or light, or hunger: these are all states of our consciousness. The difference in ourselves, says Ladd, when we are sunk in sound dreamless sleep, and when we are in full waking activity, that is consciousness. If we reason about organisms and their activities as we do about inorganic things we have no right to speak about consciousness, for outside our own Ego it has no existence. The acting animal is only a body, or a system of bodies, moving in nature, and all its activities are to be described by a system of generalised force and position co-ordinates with reference to some arbitrarily chosen point of space. “This animal machine,” says a zoologist, writing about instinct, “which I call my wife, exhibits certain facial contortions and emits certain articulate sounds which correspond with those emitted by myself when I have a headache, but I have no right to say that she has a headache.” This kind of argument does not appear to be capable of refutation except, perhaps, by the domestic conflicts which it would usually evoke if applied in such cases as that quoted. In a description of nature by the methods and symbolism of science we see only systems of molecules in motion, and in those systems which we describe as organisms the motions are only more complex than they are in inorganic systems. Such is the method of science, as irrefutable in the study of the organism as we know that it is false. Valid in pure speculation according to the methods of the intellect it would nevertheless be absurd in the everyday affairs of common civilised life and the scientific man who applies it in his writing would nevertheless hesitate to apply it in the affairs of his own household.

We must recognise that our knowledge that other beings like ourselves, as well as animals lower in organisation than ourselves, are consciously acting organisms is intuitive knowledge, attainable because of community of organisation: our intuitive knowledge of the behaviour and feelings of our own brothers and sisters is greater than our knowledge of other men and women; and we can, by intuition, place ourselves within the consciousness of an intelligent dog to a greater extent than in the case of other animals. This knowledge of the consciousness of other animals is not scientific knowledge and it is unattainable and unprovable by reasoning or methods of scientific observation. It is a conviction in itself incapable of analysis or proof, but yet a conviction on which we confidently base most of our dealings with our fellow-creatures, and which is justified by our experience.

It is nevertheless a scientific hypothesis of much the same validity as many other scientific hypotheses. We cannot bring ourselves to doubt that other men and women are consciously acting organisms, however impossible it may be to adduce scientific reason for the faith that is in us. We cannot doubt that a compass needle which “responds” by turning one or other of its poles towards us according as we push forwards one or other of the poles of a magnet is an unconscious piece of metal, though we find it impossible to say why this belief possesses such conviction. From this to the movements of the typical green plant is only a step. The turning of a green leaf towards the source of light, or the downward movement of a root into the soil, are responses to external stimuli which exhibit most of the inevitability of response of the magnet. They are “tropisms”: the plant leaf is obliged to turn towards the light so that the latter strikes against its surface perpendicularly, and the root must grow downwards because gravity acts along vertical lines. But suppose that reflex actions are tropistic: suppose, for instance, that the moth is bound to fly into the candle flame because the light stimulates both sides of its body equally and this orientates it and guides it towards the direction from which the stimulus proceeds. Complex actions, in the higher animal, on this view are chains of reflexes, and the acting must be unconscious and inevitable, just as the turning of the magnet or green leaf are unconscious movements. Therefore the actions of our fellow-creatures are unconscious and automatic, a conclusion toward which the whole tendency of mechanistic physiology forces us. Yet we know that the conclusion cannot be true.