85. The properties of tissues are their peculiar modes of reaction, and each tissue has its dominant characteristic, such as the Contractility of the muscle, and the Neurility of the nerve. But there has of late years sprung up a misleading conception, partly a consequence of the cell-theory, and partly of the almost inevitable tendency of analysis to disregard whatever elements it provisionally sets aside; this conception is the removal of the property from its tissue, and the localization of it in one of the organites—cell or fibre. This has been conspicuously mischievous in the case of the nerve-cell, which has been endowed with mysterious powers, and may be said to have usurped the place of nerve-tissue. I shall have to speak of this in the next problem. Here I only warn the student against the common error. The properties of a tissue depend on the structure and composition of that tissue, together with its plasmode and products; they vary as these vary. To select any one element in this complex, and ascribe the reaction of the tissue to that, is only permissible as a shorthand expression.
86. What has just been expounded may be condensed in the following biological law:—
Identity of tissue everywhere implies identity of property; and similarity of tissue corresponding similarity of property. Identity of organic connection everywhere implies identity of function; and similarity of organic connection similarity of function.
87. This law, first formulated by me in 1859, and then applied to the interpretation of nervous functions, was so little understood that for the most part it met with either decided denial or silent neglect; no doubt because of the general disinclination to admit that the properties and functions of the spinal cord could be similar to those of the brain, in correspondence with the similarity of their tissues and organic connections. Even Professor Vulpian, who adopted it, as well as my principal interpretations, hesitated, and relapsed into the orthodox view in assigning three different properties to one and the same tissue in cord, medulla oblongata, and cerebrum.[38] In the course of our inquiries we shall so frequently have to invoke this law that I earnestly beg the reader to meditate upon it, and ask himself upon what other grounds, save those of structure and connection, the properties and functions can possibly rest? If on no other, then similarity in structure and connection by logical necessity involves similarity in property and function.
DOES THE FUNCTION DETERMINE THE ORGAN?
88. Closely connected with this law, which simply formulates the self-evident principle that every action is rigorously determined by the nature of the agent, and the conditions under which the act takes place, is the surprising question whether functions are dependent upon organs, or organs dependent on functions?—a question which sometimes takes this shape: Is Life the result of organization, or is organization the result of Life?
The vitalist, who holds that Life is an extra-organic agent, is logical in declaring organization to be the consequence of Life;[39] but there are many organicists who conclude from certain facts that organs are developed by functions, and that organization is a result of Life. There seems, however, to be some equivoque here. I cannot otherwise understand how Mr. Spencer should have written: “There is one fact implying that Function must be regarded as taking the precedence of Structure. Of the lowest rhizopods which present no distinctions of parts, and nevertheless feed and grow and move about, Professor Huxley has remarked that they exhibit Life without Organization.”[40] The equivoque here arises from the practice of calling all living bodies “organisms,” even those destitute of the differentiations called organs; but if we substitute the term “living body” in lieu of “organism,” the equivoque will disappear, and Function no longer seem to precede Structure. Neither Mr. Spencer nor Mr. Huxley would affirm that Life can be manifested without a living body; and every living body must have a structure of some sort—unless by structure be meant a special configuration of parts. The properties of a body, whether it be simple or complex in structure, result from the properties of its components; and the vital phenomena vary with these varying components. The substance of a Rhizopod is indeed simple as compared with that of higher organisms, but is complex as compared with anorganisms; and corresponding with this simplicity of structure there is simplicity of vital function.[41]
89. The properties of steam are exhibited by the kettle on the fire, no less than by the gigantic engine which animates a manufactory; but the uses of steam (the functions of the engine) vary with the varying structure, and the applications of that structure to other structures. Precisely analogous is the case of the organ and its function, in relation to the living substance of which it is a peculiar modification. Vital actions are manifested by a lump of protoplasm; but these actions are as sharply demarcated from the actions of more highly organized animals, as the phenomena of a steam-engine are from those of a teakettle.
90. Mr. Spencer has nowhere defined what he means by Structure, nor given a definition of Organ, and this neglect makes it difficult rightly to appreciate his view. But whether we take structure to signify the substance of the living body, or the differentiations of that substance into separate tissues and organs, in either case the actions (functions) of which this structure is the agent must be rigorously determined by it. Mr. Spencer has avowed this in declaring that the “general physiologist may consider functions in their widest sense as the correlatives of tissue.” Is this true in the widest sense and not true in the narrowest? I am puzzled to find him insisting that “function from beginning to end is the determining cause of structure. Not only is this manifestly true where the modification of structure arises by reaction from modification of function; but it is also true where a modification of structure otherwise produced apparently initiates a modification of function.” Such language would be consistent were he a vitalist who believed in a Principle independent of Matter which shapes matter into organic forms; but as a positive thinker he can scarcely escape the admission that since Function is the activity of the Agent (Function in the widest sense being the action of the whole Organism, and in its narrowest sense the action of the special Organ) there cannot be an activity preceding the agent. I suspect that he does not always bear in mind the distinction between Property and Function, and consequently is led into statements at variance with the principles he professes. As far as I understand the course of his thought, it runs somewhat thus: With the increased use of an organ its volume may be increased, its structure altered; this alteration will, by reaction, cause alterations in other organs, and thus the result of a change in the habitual activities of an animal will be an alteration in the arrangement of its parts.
91. We speak loosely of an organ being developed by increased activity; but this is loose speech, and investigation shows that the organ is not developed by, but accompanies the increased activity, every increment of activity being necessarily preceded by a corresponding increment of structure. This is evident à priori: the force manifested is inherent in the structure manifesting it. Thus we ought not to say “the vascular system furnishes good instances of the increased growth that follows increased function”; we ought to say, “that permits increased function.” The muscle having a contractile power represented by 10, expends, we will suppose, 7 units of force in its normal activity, and these are replaced by its normal nutrition. If from an extra demand upon it 9 units are expended, the muscle becomes fatigued, if 10, exhausted, and it will no longer contract, the whole disposable sum of its contractility being dissipated. During all these stages the structure of the muscle—or to prevent all equivoque, let us say the substance of the muscle—has been changing, not indeed in any degree appreciable to the eye, but appreciable by the more decisive tests of chemical and physiological reactions. Yet inasmuch as in the ordinary course of things the waste is quickly repaired, the muscle in repose once more regains its original state, once more represents 10 units of contractility. Now let us consider what takes place when extra labor is thrown upon the muscle, when exercise causes growth. At the outset of a walking tour we may not be able to compass more than twenty miles a day, at its close we manage thirty. Is it the increased activity of the function which has caused this increase of structure? In one sense, yes; but let us understand it. Had the increase of activity been temporary, there would have been only a temporary increase of structure. But when the ordinary expenditure of 7 units rises to 9, on several successive days, this extra expenditure of tissue has had to be met by an extra nutrition—i. e. more plasmode has been formed and more protoplasm. It is a physiological law, easily explained, that, within due limits, extra waste brings about extra repair: as the channels are widened and multiplied, the derived currents become stronger, and the increased flow of nutrition which was temporary becomes permanent, because this increase is no longer dependent on an extra stimulus, but on an enlarged channel.[42] When the channels have not become multiplied or enlarged, which must be the case whenever the extra stimulus is fluctuating and temporary, the extra expenditure is not followed by increased size of the muscle: the currents resume their old directions, no longer being diverted.