Chapter XXIV

. Meanwhile we can say that the multiplicity of emotional and instinctive reactions in man, together with his extensive associative power, permit of extensive recouplings of the original sensory and motor partners. The _consequences_ of one instinctive reaction often prove to be the inciters of an opposite reaction, and being _suggested_ on later occasions by the original object, may then suppress the first reaction altogether, just as in the case of the child and the flame. For this education the hemispheres do not need to be _tabulæ rasæ_ at first, as the Meynert scheme would have them; and so far from their being educated by the lower centres exclusively, they educate themselves.[94]

We have already noticed the absence of reactions from fear and hunger in the ordinary brainless frog. Schrader gives a striking account of the instinctless condition of his brainless pigeons, active as they were in the way of locomotion and voice. "The hemisphereless animal moves in a world of bodies which ... are all of equal value for him.... He is, to use Goltz's apt expression, _impersonal_.... Every object is for him only a space-occupying mass, he turns out of his path for an ordinary pigeon no otherwise than for a stone. He may try to climb over both. All authors agree that they never found any difference, whether it was an inanimate body, a cat, a dog, or a bird of prey which came in their pigeon's way. The creature knows neither friends nor enemies, in the thickest company it lives like a hermit. The languishing cooing of the male awakens no more impression than the rattling of the peas, or the call-whistle which in the days before the injury used to make the birds hasten to be fed. Quite as little as the earlier observers have I seen hemisphereless she-birds answer the courting of the male. A hemisphereless male will coo all day long and show distinct signs of sexual excitement, but his activity is without any object, it is entirely indifferent to him whether the she-bird be there or not. If one is placed near him, he leaves her unnoticed.... As the male pays no attention to the female, so she pays none to her young. The brood may follow the mother ceaselessly calling for food, but they might as well ask it from a stone.... The hemisphereless sphereless pigeon is in the highest degree tame, and fears man as little as cat or bird of prey."[95]

Putting together now all the facts and reflections which we have been through, it seems to me that _we can no longer hold strictly to the Meynert scheme_. If anywhere, it will apply to the lowest animals; but in them especially the lower centres seem to have a degree of spontaneity and choice. On the whole, I think that we are driven to substitute for it some such general conception as the following, which allows for zoological differences as we know them, and is vague and elastic enough to receive any number of future discoveries of detail.

CONCLUSION.

All the centres, in all animals, whilst they are in one aspect mechanisms, probably are, or at least once were, organs of consciousness in another, although the consciousness is doubtless much more developed in the hemispheres than it is anywhere else. The consciousness must everywhere _prefer_ some of the sensations which it gets to others; and if it can remember these in their absence, however dimly, they must be its _ends_ of desire. If, moreover, it can identify in memory any motor discharges which may have led to such ends, and associate the latter with them, then these motor discharges themselves may in turn become desired as _means_. This is the development of _will_; and its realization must of course be proportional to the possible complication of the consciousness. Even the spinal cord may possibly have some little power of will in this sense, and of effort towards modified behavior in consequence of new experiences of sensibility.[96]

All nervous centres have then in the first instance one essential function, that of 'intelligent' action. They feel, prefer one thing to another, and have 'ends.' Like all other organs, however, they _evolve_ from ancestor to descendant, and their evolution takes two directions, the lower centres passing downwards into more unhesitating automatism, and the higher ones upwards into larger intellectuality.[97] Thus it may happen that those functions which can safely grow uniform and fatal become least accompanied by mind, and that their organ, the spinal cord, becomes a more and more soulless machine; whilst on the contrary those functions which it benefits the animal to have adapted to delicate environing variations pass more and more to the hemispheres, whose anatomical structure and attendant consciousness grow more and more elaborate as zoological evolution proceeds. In this way it might come about that in man and the monkeys the basal ganglia should do fewer things by themselves than they can do in dogs, fewer in dogs than in rabbits, fewer in rabbits than in hawks,[98] fewer in hawks than in pigeons, fewer in pigeons than in frogs, fewer in frogs than in fishes, and that the hemispheres should correspondingly do more. This passage of functions forward to the ever-enlarging hemispheres would be itself one of the evolutive changes, to be explained like the development of the hemispheres themselves, either by fortunate variation or by inherited effects of use. The reflexes, on this view, upon which the education of our human hemispheres depends, would not be due to the basal ganglia alone. They would be tendencies in the hemispheres themselves, modifiable by education, unlike the reflexes of the medulla oblongata, pons, optic lobes and spinal cord. Such cerebral reflexes, if they exist, form a basis quite as good as that which the Meynert scheme offers, for the acquisition of memories and associations which may later result in all sorts of 'changes of partners' in the psychic world. The diagram of the baby and the candle (see page 25) can be re-edited, if need be, as an entirely cortical transaction. The original tendency to touch will be a cortical instinct; the burn will leave an image in another part of the cortex, which, being recalled by association, will inhibit the touching tendency the next time the candle is perceived, and excite the tendency to withdraw--so that the retinal picture will, upon that next time, be coupled with the original motor partner of the pain. We thus get whatever psychological truth the Meynert scheme possesses without entangling ourselves on a dubious anatomy and physiology.

Some such shadowy view of the evolution of the centres, of the relation of consciousness to them, and of the hemispheres to the other lobes, is, it seems to me, that in which it is safest to indulge. If it has no other advantage, it at any rate makes us realize how enormous are the gaps in our knowledge, the moment we try to cover the facts by any one formula of a general kind.

FOOTNOTES:

[4] It should be said that this particular cut commonly proves fatal. The text refers to the rare cases which survive.

[5] I confine myself to the frog for simplicity's sake. In higher animals, especially the ape and man, it would seem as if not only determinate combinations of muscles, but limited groups or even single muscles could be innervated from the hemispheres.

[6] I hope that the reader will take no umbrage at my so mixing the physical and mental, and talking of reflex acts and hemispheres and reminiscences in the same breath, as if they were homogeneous quantities and factors of one causal chain. I have done so deliberately; for although I admit that from the radically physical point of view it is easy to conceive of the chain of events amongst the cells and fibres as complete in itself, and that whilst so conceiving it one need make no mention of 'ideas,' I yet suspect that point of view of being an unreal abstraction. Reflexes in centres may take place even where accompanying feelings or ideas guide them. In another