The Principles of Biology, Volume 1 (of 2). Spencer Herbert. Читать онлайн. Newlib. NEWLIB.NET

Автор: Spencer Herbert
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proceeding from those parts. Indeed, looked at from this point of view, the two classes of nervous changes – the one initiated from without and the other from within – are seen to merge into one class. Both of them may be traced to metamorphosis of tissue. The sensations of touch and pressure are doubtless consequent on accelerated changes of matter, produced by mechanical disturbance of the mingled fluids and solids composing the parts affected. There is abundant evidence that the gustatory sensation is due to the chemical actions set up by particles which find their way through the membrane covering the nerves of taste; for, as Prof. Graham points out, sapid substances belong to the class of crystalloids, which are able rapidly to permeate animal tissue, while the colloids which cannot pass through animal tissue are insipid. Similarly with the sense of smell. Substances which excite this sense are necessarily more or less volatile; and their volatility being the result of their molecular mobility, implies that they have, in a high degree, the power of getting at the olfactory nerves by penetrating their mucous investment. Again, the facts which photography has familiarized us with, show that those nervous impressions called colours, are primarily due to certain changes wrought by light in the substance of the retina. And though, in the case of hearing, we cannot so clearly trace the connexion of cause and effect, yet as we see that the auditory apparatus is one fitted to intensify those vibrations constituting sound, and to convey them to a receptacle containing liquid in which nerves are immersed, it can scarcely be doubted that the sensation of sound proximately results from molecular re-arrangements caused in these nerves by the vibrations of the liquid: knowing, as we do, that the re-arrangement of molecules is in all cases aided by agitation. Perhaps, however, the best proof that nerve-force, whether peripheral or central in origin, results from chemical change, lies in the fact that most of the chemical agents which powerfully affect the nervous system, affect it whether applied at the centre or at the periphery. Various mineral acids are tonics – the stronger ones being usually the stronger tonics; and this which we call their acidity implies a power in them of acting on the nerves of taste, while the tingling or pain following their absorption through the skin, implies that the nerves of the skin are acted on by them. Similarly with certain vegeto-alkalies which are peculiarly bitter. By their bitterness these show that they affect the extremities of the nerves, while, by their tonic properties, they show that they affect the nervous centres: the most intensely bitter among them, strychnia, being the most powerful nervous stimulant.11 However true it may be that this relation is not a regular one, since opium, hashish, and some other drugs, which work marked effects on the brain, are not remarkably sapid – however true it may be that there are relations between particular substances and particular parts of the nervous system; yet such instances do but qualify, without negativing, the general proposition. The truth of this proposition can scarcely be doubted when, to the facts above given, is added the fact that various condiments and aromatic drugs act as nervous stimulants; and the fact that anæsthetics, besides the general effects they produce when inhaled or swallowed, produce local effects of like kind – first stimulant and then sedative – when absorbed through the skin; and the fact that ammonia, which in consequence of its extreme molecular mobility so quickly and so violently excites the nerves beneath the skin, as well as those of the tongue and the nose, is a rapidly-acting stimulant when taken internally.

      Whether a nerve is merely a conductor, which delivers at one of its extremities an impulse received at the other, or whether, as some now think, it is itself a generator of force which is initiated at one extremity and accumulates in its course to the other extremity, are questions which cannot yet be answered. All we know is that agencies capable of working molecular changes in nerves are capable of calling forth from them manifestations of activity. And our evidence that nerve-force is thus originated, consists not only of such facts as the above, but also of more conclusive facts established by direct experiments on nerves – experiments which show that nerve-force results when the cut end of a nerve is either mechanically irritated, or acted on by some chemical agent, or subject to the galvanic current – experiments which prove that nerve-force is generated by whatever disturbs the molecular equilibrium of nerve-substance.

      § 22. The most important of the re-actions called forth from organisms by surrounding actions, remains to be noticed. To the various forms of insensible motion thus caused, we have to add sensible motion. On the production of this mode of force more especially depends the possibility of all vital phenomena. It is, indeed, usual to regard the power of generating sensible motion as confined to one out of the two organic sub-kingdoms; or, at any rate, as possessed by but few members of the other. On looking closer into the matter, however, we see that plant-life as well as animal-life, is universally accompanied by certain manifestations of this power; and that plant-life could not otherwise continue.

      Through the humblest, as well as through the highest, vegetal organisms, there are ever going on certain re-distributions of matter. In Protophytes the microscope shows us an internal transposition of parts, which, when not immediately visible, is proved to exist by the changes of arrangement that become manifest in the course of hours and days. In the individual cells of many higher plants, an active movement among the contained granules may be witnessed. And well-developed cryptogams, in common with all phanerogams, exhibit this genesis of mechanical motion still more conspicuously in the circulation of sap. It might, indeed, be concluded a priori, that through plants displaying much differentiation of parts, an internal movement must be going on; since, without it, the mutual dependence of organs having unlike functions would be impossible. Besides keeping up these motions of liquids internally, plants, especially of the lower orders, move their external parts in relation to each other, and also move about from place to place. There are countless such illustrations as the active locomotion of the zoospores of many Algæ, the rhythmical bendings of the Oscillatoræ, the rambling progression of the Diatomaceæ. In fact many of these smallest vegetals, and many of the larger ones in their early stages, display a mechanical activity not distinguishable from that of the simplest animals. Among well-organized plants, which are never locomotive in their adult states, we still not unfrequently meet with relative motions of parts. To such familiar cases as those of the Sensitive plant and the Venus' fly-trap, many others may be added. When its base is irritated the stamen of the Berberry flower leans over and touches the pistil. If the stamens of the wild Cistus be gently brushed with the finger, they spread themselves: bending away from the seed-vessel. And some of the orchid-flowers, as Mr. Darwin has shown, shoot out masses of pollen on to the entering bee, when its trunk is thrust down in search of honey.

      Though the power of moving is not, as we see, a characteristic of animals alone, yet in them, considered as a class, it is manifested to an extent so marked as practically to become their most distinctive trait. For it is by their immensely greater ability to generate mechanical motion, that animals are enabled to perform those actions which constitute their visible lives; and it is by their immensely greater ability to generate mechanical motion, that the higher orders of animals are most obviously distinguished from the lower orders. Though, on remembering the seemingly active movements of infusoria, some will perhaps question this last-named contrast, yet, on comparing the quantities of matter propelled through given spaces in given times, they will see that the momentum evolved is far less in the Protozoa than in the Metazoa. These sensible motions of animals are effected in sundry ways. In the humblest forms, and even in some of the more developed forms which inhabit the water, locomotion results from the oscillations of whip-like appendages, single or double, or from the oscillations of cilia: the contractility resides in these waving hairs that grow from the surface. In many Cœlenterata certain elongations or tails of ectodermal or endodermal cells shorten when stimulated, and by these rudimentary contractile organs the movements are effected. In all the higher animals, however, and to a smaller degree in many of the lower, sensible motion is generated by a special tissue, under a special excitement. Though it is not strictly true that such animals show no sensible motions otherwise caused, since all of them have certain ciliated membranes, and since the circulation of liquids in them is partially due to osmotic and capillary actions; yet, generally speaking, we may say that their movements are effected solely by muscles which contract solely through the agency of nerves.

      What special transformations of force generate these various mechanical changes, we do not, in most cases, know. Those re-distributions of liquid, with the alterations of form sometimes caused by them, that result from osmose,


<p>11</p>

When writing this passage I omitted to observe the verification yielded of the conclusion contained in § 15 concerning the part played in the vital processes by the nitrogenous compounds. For these vegeto-alkalies, minute quantities of which produce such great effects in exalting the functions (e. g., a sixteenth of a grain of strychnia is a dose), are all nitrogenous bodies, and, by implication, relatively unstable bodies. The small amounts of molecular change which take place in these small quantities of the vegeto-alkalies when diffused through the system, initiate larger amounts of molecular change in the nitrogenous elements of the tissues.

But the evidence furnished a generation ago by these vegeto-alkalies has been greatly reinforced by far more striking evidence furnished by other nitrogenous compounds – the various explosives. These, at the same time that they produce by their sudden decompositions violent effects outside the organism, also produce violent effects inside it: a hundredth of a grain of nitro-glycerine being a sufficient dose. Investigations made by Dr. J. B. Bradbury, and described by him in the Bradshaw Lecture on "Some New Vaso-Dilators" (see The Lancet, Nov. 16, 1895), details the effects of kindred bodies – methyl-nitrate, glycol-dinitrate, erythrol-tetranitrate. The first two, in common with nitro-glycerine, are stable only when cool and in the dark – sunlight or warmth decomposes them, and they explode by rapid heating or percussion. The fact which concerns us here is that the least stable – glycol-dinitrate – has the most powerful and rapid physiological effect, which is proportionately transient. In one minute the blood-pressure is reduced by one-fourth and in four minutes by nearly two-thirds: an effect which is dissipated in a quarter of an hour. So that this excessively unstable compound, decomposing in the body in a very short time, produces within that short time a vast amount of molecular change: acting, as it seems, not through the nervous system, but directly on the blood-vessels.