independent action. Open the butterfly, and you find the thirteen ganglia greatly changed: the second and third are fused into one; the fourth, fifth, and sixth into another; the eleventh and twelfth into another; the only trace of the original separation is in a slight constriction of the surface. The movements of the caterpillar were few, simple, slow, and those of the butterfly are many, varied, and rapid.

20. In the Vertebrates the coalescence of ganglia is such that the spinal axis is one great centre. We do indeed anatomically and physiologically subdivide it into several centres, because several portions directly innervate separate organs; but its importance lies in the intimate blending of all parts, so that fluctuating combinations of its elements may arise, and varied movements result. Each centre combines various muscles; the axis is a combination of centres. The brainless frog, for instance, has still the spinal cord, and therefore the power not only of moving either of his limbs, but also of combining their separate movements: if grasped, he struggles and escapes; if pricked, he hops away. But these actions, although complex, are much less complex and varied than the actions of the normal frog.

There is not only a coalescence of ganglia, but a greater and greater concentration of the substance in the upper portions of the axis. In the inferior vertebrates, and in the mammalian embryo, the spinal cord occupies the whole length of the vertebral canal from the head to the tip of the tail; and here the centres of reflexion correspond with the several segments. But as the cranial mass develops there is a withdrawal of neural substance from the lower parts, and the centres of reflexion are then some way removed from the segments they innervate. In the animal development there is even a greater and greater predominance of the upper portions, so that the

brain and medulla oblongata are of infinitely more importance than the spinal cord.

21. Besides the central group of elements which belong to fixed and definite actions, we must conceive these elements capable of variable combinations, like the pieces of colored glass in a kaleidoscope, which fall into new groups, each group having its definite though temporary form. The elements constitute really a continuous network of variable forms. It is to such combinations, and not to fixed circumscribed ganglia, that we must refer the subordinate centres of the axis. We speak of a centre for Respiration, a centre for Laughing, a centre for Crying, a centre for Coughing, and so on, with as much propriety as we speak of a centre for Swallowing or for Walking. Not that in these cases there is a circumscribed mass of central substance set apart for the innervation of the several muscles employed in these actions, and for no other purpose. Each action demands a definite group of neural elements, as each geometric form in the kaleidoscope demands a definite group of pieces of glass; but these same pieces of glass will readily enter into other combinations; and in like manner the muscles active in Respiration are also active in Laughing, Coughing, etc., though differently innervated and co-ordinated.

22. The physiological rank of a centre is therefore the expression of its power of fluctuating combination. The medulla oblongata is higher than the medulla spinalis, because of its more varied combinations; the cerebrum is higher than all, because it has no fixed and limited combinations. It is the centre of centres, and as such the supreme organ."

CHAPTER II.

THE FUNCTIONAL RELATIONS OF THE NERVOUS SYSTEM.

23. THE distinguishable parts of this system are the central axis, the cranial nerves, and the spinal nerves, with the chain of ganglia and nerves composing the Sympathetic. Let us briefly set down what is known of their special offices.

Men very early discovered that the nerves were in some way ministrant to Sensation and Movement; a divided nerve always being accompanied by insensibility and immobility in the limb. Galen, observing that paralysis of movement sometimes occurred without insensibility, suggested that there were two kinds of nerve; but no one

Fig. 12. Transverse sections of spinal cord (dorsal region).

was able to furnish satisfactory evidence in support of this suggestion until early in the present century, when the experiments of Charles Bell, perfected by those of Majendie and Müller, placed the suggestion beyond dispute.

24. Fig. 12 is a diagram (not a drawing of the actual aspect, which would be hardly intelligible to readers unversed in such matters) representing two transverse sections of the spinal cord just where the nerve-roots issue. The gray substance is somewhat in the form of a rude H, in the dorsal region, and of the expanded wings of a butterfly in the lumbar enlargements (Figs. 4-6); the extremities of this gray substance are the anterior and posterior horns. We have already said that from the anterior horns of each half issue the roots of the motor nerves, which pass to the muscles. From the posterior horns issue the sensory nerves, which, soon after leaving the cord, enter the ganglia before joining the motor nerves, and then pass to the skin, in the same sheath with their companions, separating again as they reach the muscles and surfaces. where they are to be distributed. When this mixed nerve is cut through, or tied, all sensation and movement disappear from the parts innervated. But if only one of the roots be cut through, above the ganglion, there will then be only a loss of movement or a loss of sensation. Thus suppose the section be made at a, b, A: we have then divided a sensory nerve, and no pinching or pricking of the part innervated by that nerve will be felt; but movement will take place if the under nerve be irritated, or if a sensation elsewhere be excited. Now reverse the experiment, as at B, c, d. Then, pricking of the skin will be felt, but no movement will respond. The nerve which enters the cord at the upper (posterior) part is therefore a sensory nerve; that which enters at the under (anterior) part is motor. The direction is in each case indicated by

the arrow. The central end b, if irritated, will produce sensation; whereas the peripheral end a produces neither sensation nor movement. The central end d produces neither sensation nor movement; the peripheral end c produces movement.

25. Two facts are proved by these experiments. First, that the co-operation of the centre is necessary for Sensation, but not for Movement. Although normally all the muscles of the trunk are moved only when their centre has been excited, yet any irritation applied directly to the muscle nerve, even when separated from its centre, produces a movement. And to this we may add that a slighter stimulus will move the muscle by direct irritation of the nerve, than by indirect irritation through the centre; a slighter stimulus also will suffice when applied to the nerve than when applied to the muscle itself.

26. The second fact proved is known as Bell's Law, that the sensory and motor channels are respectively the posterior and anterior nerves. The fact is indisputable, but its theoretic interpretation can no longer be accepted in its original form. Bell supposed the two nerves to be different in kind, endowed with different specific energies, the one sensitive, the other motor. The majority of writers still express themselves as if they adopted this view. We shall, however, presently see reason for replacing it by the more consistent interpretation which assigns one and the same property to both nerves, marking their distinction by the terms afferent and efferent; the one set being anatomically so disposed that it conveys stimuli from the surfaces to the centre, and the other set conveying stimuli from the centre to the muscles, glands, and other cells.*

It has been proved that the cells of the cornea and the pigment cells of the skin contract under nervous excitation. We cannot suppose that although these are the only cells which have hitherto been brought under