Chapter 41

With but little break we come here upon a significant analogy, parallel to an analogy already described. As was pointed out, an inorganic body that is modifiable by its medium, acquires, after a time, an outer coat which has already undergone such change as surrounding agencies can effect; has a contained mass which is as yet unchanged, because unreached; and has a surface between the two where change is going on--a region of activity. And we saw that alike in the vegetal cell and the animal cell there exist analogous distributions: of course with the difference that the innermost part is not inert. Now we have to note that in those aggregates of cells constituting the _Metaphyta_ and _Metazoa_, analogous distributions also exist. In plants they are of course not to be looked for in leaves and other deciduous portions, but only in portions of long duration--stems and branches. Naturally, too, we need not expect them in plants having modes of growth which early produce an outer practically dead part, that effectually shields the inner actively living part of the stem from the influence of the medium--long-lived acrogens such as tree-ferns and long-lived endogens such as palms. But in the highest plants, exogens, which have the actively living part of their stems within reach of environing agencies, we find this part,--the cambium layer,--is one from which there is a growth inwards forming wood, and a growth outwards forming bark: there is an increasingly thick covering (where it does not scale off) of tissue changed by the medium, and inside this a film of highest vitality. In so far as concerns the present argument, it is the same with the _Metazoa_, or at least all of them which have developed organizations. The outer skin grows up from a limiting plane, or layer, a little distance below the surface--a place of predominant vital activity. Here perpetually arise new cells, which, as they develop, are thrust outwards and form the epidermis: flattening and drying up as they approach the surface, whence, having for a time served to shield the parts below, they finally scale off and leave younger ones to take their places. This still undifferentiated tissue forming the base of the epidermis, and existing also as a source of renewal in internal organs, is the essentially living substance; and facts above given imply that it was the action of the medium on this essentially living substance, which, during early stages in the organization of the _Metazoa_, initiated that protective envelope which presently became an inherited structure--a structure which, though now mainly inherited, still continues to be modifiable by its initiator.

Fully to perceive the way in which these evidences compel us to recognize the influence of the medium as a primordial factor, we need but conceive them as interpreted without it. Suppose, for instance, we say that the structure of the epidermis is wholly determined by the natural selection of favourable variations; what must be the position taken in presence of the fact above named, that when mucous membrane is exposed to the air its cell-structure changes into the cell-structure of skin? The position taken must be this:--Though mucous membrane in a highly-evolved individual organism, thus shows the powerful effect of the medium on its surface; yet we must not suppose that the medium had the effect of producing such a cell-structure on the surfaces of primitive forms, undifferentiated though they were; or, if we suppose that such an effect was produced on them, we must not suppose that it was inheritable. Contrariwise, we must suppose that such effect of the medium either was not wrought at all, or that it was evanescent: though repeated through millions upon millions of generations it left no traces. And we must conclude that this skin-structure arose only in consequence of spontaneous variations not physically initiated (though like those physically initiated) which natural selection laid hold of and increased. Does any one think this a tenable position?

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And now we approach the last and chief series of morphological phenomena which must be ascribed to the direct action of environing matters and forces. These are presented to us when we study the early stages in the development of the embryos of the _Metazoa_ in general.

We will set out with the fact already noted in passing, that after repeated spontaneous fissions have changed the original fertilized germ-cell into that cluster of cells which forms a gemmule or a primitive ovum, the first contrast which arises is between the peripheral parts and the central parts. Where, as with lower creatures which do not lay up large stores of nutriment with the germs of their offspring, the inner mass is inconsiderable, the outer layer of cells, which are presently made quite small by repeated subdivisions, forms a membrane extending over the whole surface--the blastoderm. The next stage of development, which ends in this covering layer becoming double, is reached in two ways--by invagination and by delamination; but which is the original way and which the abridged way, is not quite certain. Of invagination, multitudinously exemplified in the lowest types, Mr. Balfour says:--"On purely _à priori_ grounds there is in my opinion more to be said for invagination than for any other view";[57] and, for present purposes, it will suffice if we limit ourselves to this: making its nature clear to the general reader by a simple illustration.

Take a small india-rubber ball--not of the inflated kind, nor of the solid kind, but of the kind about an inch or so in diameter with a small hole through which, under pressure, the air escapes. Suppose that instead of consisting of india-rubber its wall consists of small cells made polyhedral in form by mutual pressure, and united together. This will represent the blastoderm. Now with the finger, thrust in one side of the ball until it touches the other: so making a cup. This action will stand for the process of invagination. Imagine that by continuance of it, the hemispherical cup becomes very much deepened and the opening narrowed, until the cup becomes a sac, of which the introverted wall is everywhere in contact with the outer wall. This will represent the two-layered "gastrula"--the simplest ancestral form of the _Metazoa_: a form which is permanently represented in some of the lowest types; for it needs but tentacles round the mouth of the sac, to produce a common hydra. Here the fact which it chiefly concerns us to remark, is that of these two layers the outer, called in embryological language the epiblast, continues to carry on direct converse with the forces and matters in the environment; while the inner, called the hypoblast, comes in contact with such only of these matters as are put into the food-cavity which it lines. We have further to note that in the embryos of _Metazoa_ at all advanced in organization, there arises between these two layers a third--the mesoblast. The origin of this is seen in types where the developmental process is not obscured by the presence of a large food-yolk. While the above-described introversion is taking place, and before the inner surfaces of the resulting epiblast and hypoblast have come into contact, cells, or amoeboid units equivalent to them, are budded off from one or both of these inner surfaces, or some part of one or other; and these form a layer which eventually lies between the other two--a layer which, as this mode of formation implies, never has any converse with the surrounding medium and its contents, or with the nutritive bodies taken in from it. The striking facts to which this description is a necessary introduction, may now be stated. From the outer layer, or epiblast, are developed the permanent epidermis and its out-growths, the nervous system, and the organs of sense. From the introverted layer, or hypoblast, are developed the alimentary canal and those parts of its appended organs, liver, pancreas, &c., which are concerned in delivering their secretions into the alimentary canal, as well as the linings of those ramifying tubes in the lungs which convey air to the places where gaseous exchange is effected. And from the mesoblast originate the bones, the muscles, the heart and blood-vessels, and the lymphatics, together with such parts of various internal organs as are most remotely concerned with the outer world. Minor qualifications being admitted, there remain the broad general facts, that out of that part of the external layer which remains permanently external, are developed all the structures which carry on intercourse with the medium and its contents, active and passive; out of the introverted part of this external layer, are developed the structures which carry on intercourse with the quasi-external substances that are taken into the interior--solid food, water, and air; while out of the mesoblast are developed structures which have never had, from first to last, any intercourse with the environment. Let us contemplate these general facts.

Who would have imagined that the nervous system is a modified portion of the primitive epidermis? In the absence of proofs furnished by the concurrent testimony of embryologists during the last thirty or forty years, who would have believed that the brain arises from an infolded tract of the outer skin, which, sinking down beneath the surface, becomes imbedded in other tissues and eventually surrounded by a bony case? Yet the human nervous system in common with the nervous systems of lower animals is thus originated. In the words of Mr. Balfour, early embryological changes imply that--

"the functions of the central nervous system, which were originally taken by the whole skin, became gradually concentrated in a special part of the skin which was step by step removed from the surface, and has finally become in the higher types a well-defined organ imbedded in the subdermal tissues.... The embryological evidence shows that the ganglion-cells of the central part of the nervous system are originally derived from the simple undifferentiated epithelial cells of the surface of the body."[58]

Less startling perhaps, though still startling enough, is the fact that the eye is evolved out of a portion of the skin; and that while the crystalline lens and its surroundings thus originate, the "percipient portions of the organs of special sense, especially of optic organs, are often formed from the same part of the primitive epidermis" which forms the central nervous system.[59] Similarly is it with the organs for smelling and hearing. These, too, begin as sacs formed by infoldings of the epidermis; and while their parts are developing they are joined from within by nervous structures which were themselves epidermic in origin. How are we to interpret these strange transformations? Observing, as we pass, how absurd from the point of view of the special-creationist, would appear such a filiation of structures, and such a round-about mode of embryonic development, we have here to remark that the process is not one to have been anticipated as a result of natural selection. After numbers of spontaneous variations had occurred, as the hypothesis implies, in useless ways, the variation which primarily initiated a nervous centre might reasonably have been expected to occur in some internal part where it would be fitly located. Its initiation in a dangerous place and subsequent migration to a safe place, would be incomprehensible. Not so if we bear in mind the cardinal truth above set forth, that the structures for holding converse with the medium and its contents, arise in that completely superficial part which is directly affected by the medium and its contents; and if we draw the inference that the external actions themselves initiate the structures. These once commenced, and furthered by natural selection where favourable to life, would form the first term of a series ending in developed sense organs and a developed nervous system.[60]

Though it would enforce the argument, I must, for brevity's sake, pass over the analogous evolution of that introverted layer, or hypoblast, out of which the alimentary canal and attached organs arise. It will suffice to emphasize the fact that having been originally external, this layer continues in its developed form to have a quasi-externality, alike in its digesting part and in its respiratory part; since it continues to deal with matters alien to the organism. I must also refrain from dwelling at length on the fact already adverted to, that the intermediate derived layer, or mesoblast, which was at the outset completely internal, originates those structures which ever remain completely internal, and have no communication with the environment save through the structures developed from the other two: an antithesis which has great significance.

Here, instead of dwelling on these details, it will be better to draw attention to the most general aspect of the facts. Whatever may be the course of subsequent changes, the first change is the formation of a superficial layer or blastoderm; and by whatever series of transformations the adult structure is reached, it is from the blastoderm that all the organs forming the adult originate. Why this marvellous fact?

Meaning is given to it if we go back to the first stage in which _Protozoa_, having by repeated fissions formed a cluster, then arranged themselves into a hollow sphere, as do the protophytes forming a _Volvox_. Originally alike all over its surface, the hollow sphere of ciliated units thus formed, would, if not quite spherical, assume a constant attitude when moving through the water; and hence one part of the spheroid would more frequently than the rest come in contact with nutritive matters to be taken in. A division of labour resulting from such a variation being advantageous, and tending therefore to increase in descendants, would end in a differentiation like that shown in the gemmules of various low types of _Metazoa_, which, ovate in shape, are ciliated over one part of the surface only. There would arise a form in which the cilium-bearing units effected locomotion and aeration; while on the others, assuming an amoeba-like character, devolved the function of absorbing food: a primordial specialization variously indicated by evidence.[61] Just noting that an ancestral origin of this kind is implied by the fact that in low types of _Metazoa_ a hollow sphere of cells is the form first assumed by the unfolding embryo, I draw attention to the point here of chief interest; namely that the primary differentiation of this hollow sphere is in such case determined by a difference in the converse of its parts with the medium and its contents; and that the subsequent invagination arises by a continuance of this differential converse.

Even neglecting this first stage and commencing with the next, in which a "gastrula" has been produced by the permanent introversion of one portion of the surface of the hollow sphere, it will suffice if we consider what must thereafter have happened. That which continued to be the outer surface was the part which from time to time touched quiescent masses and occasionally received the collisions consequent on its own motions or the motions of other things. It was the part to receive the sound-vibrations occasionally propagated through the water; the part to be affected more strongly than any other by those variations in the amounts of light caused by the passing of small bodies close to it; and the part which met those diffused molecules constituting odours. That is to say, from the beginning the surface was the part on which there fell the various influences pervading the environment, the part by which there was received those impressions from the environment serving for the guidance of actions, and the part which had to bear the mechanical re-actions consequent upon such actions. Necessarily, therefore, the surface was the part in which were initiated the various instrumentalities for carrying on intercourse with the environment. To suppose otherwise is to suppose that such instrumentalities arose internally where they could neither be operated on by surrounding agencies nor operate on them,--where the differentiating forces did not come into play, and the differentiated structures had nothing to do; and it is to suppose that meanwhile the parts directly exposed to the differentiating forces remained unchanged. Clearly, then, organization could not but begin on the surface; and having thus begun, its subsequent course could not but be determined by its superficial origin. And hence these remarkable facts showing us that individual evolution is accomplished by successive in-foldings and in-growings. Doubtless natural selection soon came into action, as, for example, in the removal of the rudimentary nervous centres from the surface; since an individual in which they were a little more deeply seated would be less likely to be incapacitated by injury of them. And so in multitudinous other ways. But nevertheless, as we here see, natural selection could operate only under subjection. It could do no more than take advantage of those structural changes which the medium and its contents initiated.

See, then, how large has been the part played by this primordial factor. Had it done no more than give to _Protozoa_ and _Protophyta_ that cell-form which characterizes them--had it done no more than entail the cellular composition which is so remarkable a trait of _Metazoa_ and _Metaphyta_--had it done no more than cause the repetition in all visible animals and plants of that primary differentiation of outer from inner which it first wrought in animals and plants invisible to the naked eye; it would have done much towards giving to organisms of all kinds certain leading traits. But it has done more than this. By causing the first differentiations of those clusters of units out of which visible animals in general arose, it fixed the starting place for organization, and therefore determined the course of organization; and, doing this, gave indelible traits to embryonic transformations and to adult structures.

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Though mainly carried on after the inductive method, the argument at the close of the foregoing section has passed into the deductive. Here let us follow for a space the deductive method pure and simple. Doubtless in biology _à priori_ reasoning is dangerous; but there can be no danger in considering whether its results coincide with those reached by reasoning _à posteriori_.

Biologists in general agree that in the present state of the world, no such thing happens as the rise of a living creature out of non-living matter. They do not deny, however, that at a remote period in the past, when the temperature of the Earth's surface was much higher than at present, and other physical conditions were unlike those we know, inorganic matter, through successive complications, gave origin to organic matter. So many substances once supposed to belong exclusively to living bodies, have now been formed artificially, that men of science scarcely question the conclusion that there are conditions under which, by yet another step of composition, quaternary compounds of lower types pass into those of highest types. That there once took place gradual divergence of the organic from the inorganic, is, indeed, a necessary implication of the hypothesis of Evolution, taken as a whole; and if we accept it as a whole, we must put to ourselves the question--What were the early stages of progress which followed, after the most complex form of matter had arisen out of forms of matter a degree less complex?

At first, protoplasm could have had no proclivities to one or other arrangement of parts; unless, indeed, a purely mechanical proclivity towards a spherical form when suspended in a liquid. At the outset it must have been passive. In respect of its passivity, primitive organic matter must have been like inorganic matter. No such thing as spontaneous variation could have occurred in it; for variation implies some habitual course of change from which it is a divergence, and is therefore excluded where there is no habitual course of change. In the absence of that cyclical series of metamorphoses which even the simplest living thing now shows us, as a result of its inherited constitution, there could be no _point d'appui_ for natural selection. How, then, did organic evolution begin?

If a primitive mass of organic matter was like a mass of inorganic matter in respect of its passivity, and differed only in respect of its greater changeableness; then we must infer that its first changes conformed to the same general law as do the changes of an inorganic mass. The instability of the homogeneous is a universal principle. In all cases the homogeneous tends to pass into the heterogeneous, and the less heterogeneous into the more heterogeneous. In the primordial units of protoplasm, then, the step with which evolution commenced must have been the passage from a state of complete likeness throughout the mass to a state in which there existed some unlikeness. Further, the cause of this step in one of these portions of organic matter, as in any portion of inorganic matter, must have been the different exposure of its parts to incident forces. What incident forces? Those of its medium or environment. Which were the parts thus differently exposed? Necessarily the outside and the inside. Inevitably, then, alike in the organic aggregate and the inorganic aggregate (supposing it to have coherence enough to maintain constant relative positions among its parts), the first fall from homogeneity to heterogeneity must always have been the differentiation of the external surface from the internal contents. No matter whether the modification was physical or chemical, one of composition or of decomposition, it comes within the same generalization. The direct action of the medium was the primordial factor of organic evolution.

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And now, finally, let us look at the factors in their _ensemble_, and consider the respective parts they play: observing, especially, the ways in which, at successive stages, they severally give place one to another in degree of importance.