Relations between the aggregate and the units which are in this case permanent, are in other cases temporary: characterizing early stages of embryonic development. For example, drawings of Echinoderm larvæ at an early stage, show us the potential independence of all the cells forming the blastosphere; for in the course of further development some of these resume the primitive amœboid state, migrate through the internal space, and presently unite to form certain parts of the growing structures. But with the progress of organization independence of this kind diminishes.
Converse facts are presented after development has been completed; for with the commencement of reproduction we everywhere see more or less resumption of individual life among the units, or some of them. It is a trait of transitional types between Protozoa and Metazoa to lead an aggregate life as a plasmodium, and then for this to break up into its members, which for a time lead individual lives as generative agents; and sundry low kinds of plants possessing small amounts of structure, have generative elements – zoospores and spermatozoids – which show us a return to unit life. Nor, indeed, are we shown this only in the lowest plants; for it has recently been found that in certain of the higher plants – even in Phænogams – spermatozoids are produced. That is to say, the units resume active lives at places where the controlling influence of the aggregate is failing; for, as we shall hereafter see, places at which generation commences answer to this description.
These different kinds of evidence jointly imply that the individual lives of the units are subordinate to the general life in proportion as this is high. Where the organism is very inferior in type the unit-life remains permanently conspicuous. In some superior types there is a display of unit-life during embryonic stages in which the co-ordinating action of the aggregate is but incipient. With the advance of development the unit-life diminishes; but still, in plants, recommences where the disintegrating process which initiates generation shows the coercive power of the organization to have become small.
Even in the highest types, however, and even when they are fully developed, unit-life does not wholly disappear: it is clearly shown in ourselves. I do not refer simply to the fact that, as throughout the animal kingdom at large and a considerable part of the vegetal kingdom, the male generative elements are units which have resumed the primitive independent life, but I refer to a much more general fact. In that part of the organism which, being fundamentally an aqueous medium, is in so far like the aqueous medium in which ordinary protozoon life is carried on, we find an essentially protozoon life. I refer of course to the blood. Whether the tendency of the red corpuscles (which are originally developed from amœba-like cells) to aggregate into rouleaux is to be taken as showing life in them, may be left an open question. It suffices that the white corpuscles or leucocytes, retaining the primitive amœboid character, exhibit individual activities: send out prolongations like pseudopodia, take in organic particles as food, and are independently locomotive. Though far less numerous than the red corpuscles, yet, as ten thousand are contained in a cubic millimetre of blood – a mass less than a pin's head – it results that the human body is pervaded throughout all its blood-vessels by billions of these separately living units. In the lymph, too, which also fulfils the requirements of liquidity, these amœboid units are found. Then we have the curious transitional stage in which units partially imbedded and partially free display a partial unit-life. These are the ciliated epithelium-cells, lining the air-passages and covering sundry of the mucous membranes which have more remote connexions with the environment, and covering also the lining membranes of certain main canals and chambers in the nervous system. The inner parts of these unite with their fellows to form an epithelium, and the outer parts of them, immersed either in liquid or semi-liquid (mucus), bear cilia that are in constant motion and "produce a current of fluid over the surface they cover: " thus simulating in their positions and actions the cells lining the passages ramifying through a sponge. The partially independent lives of these units is further seen in the fact that after being detached they swim about in water for a time by the aid of their cilia.
§ 54d. But in the Metazoa and Metaphyta at large, the associated units are, with the exceptions just indicated, completely subordinated. The unit-life is so far lost in the aggregate life that neither locomotion nor the relative motion of parts remains; and neither in shape nor composition is there resemblance to protozoa. Though in many cases the internal protoplasm continues to carry on vital processes subserving the needs of the aggregate, in others vital processes of an independent kind appear to cease.
It will naturally be supposed that after recognizing this fundamental trait common to all types of organisms above the Protozoa and Protophyta, the next step in an account of structure must be a description of their organs, variously formed and combined – if not in detail yet in their general characters. This, however, is an error. There are certain truths of structure higher in generality than any which can be alleged of organs. We shall see this if we compare organs with one another.
Here is a finger stiffened by its small bones and yet made flexible by the uniting joints. There is a femur which helps its fellow to support the weight of the body; and there again is a rib which, along with others, forms a protective box for certain of the viscera. Dissection reveals a set of muscles serving to straighten and bend the fingers, certain other muscles that move the legs, and some inconspicuous muscles which, contracting every two or three seconds, slightly raise the ribs and aid in inflating the lungs. That is to say, fingers, legs, and chest possess certain structures in common. There is in each case a dense substance capable of resisting stress and a contractile substance capable of moving the dense substance to which it is attached. Hence, then, we have first to give an account of these and other chief elements which, variously joined together, form the different organs: we have to observe the general characters of tissues.
On going back to the time when the organism begins with a single cell, then becomes a spherical cluster of cells, and then exhibits differences in the modes of aggregation of these cells, the first conspicuous rise of structure (limiting ourselves to animals) is the formation of three layers. Of these the first is, at the outset and always, the superficial layer in direct contact with the environment. The second, being originally a part of the first, is also in primitive types in contact with the environment, but, being presently introverted, forms the rudiment of the food-cavity; or, otherwise arising in higher types, is in contact with the yelk or food provided by the parent. And the third, presently formed between these two, consists at the outset of cells derived from them imbedded in an intercellular substance of jelly-like consistence. Hence originate the great groups classed as epithelium-tissue, connective tissue (including osseous tissue), muscular tissue, nervous tissue. These severally contain sub-kinds, each of which is a complex of differentiated cells. Being brief, and therefore fitted for the present purposes, the sub-classification given by Prof. R. Hertwig may here be quoted; —
"The physiological character of epithelia is given in the fact that they cover the surfaces of the body, their morphological character in that they consist of closely compressed cells united only by a cementing substance.
"According to their further functional character epithelia are divided into glandular epithelia (unicellular and multicellular glands), sensory, germinal, and pavement epithelia.
"According to the structure are distinguished one-layered (cubical, cylindrical, pavement epithelia) and many-layered epithelia, ciliated and flagellated epithelia, epithelia with or without cuticle.
"The physiological character of the connective tissues rests upon the fact that they fill up spaces between other tissues in the interior of the body.
"The morphological character depends upon the presence of the intercellular substance.
"According to the quantity and the structure of the intercellular substance the connective substances are divided into (1) cellular (with little intercellular substance); (2) homogeneous; (3) fibrillar connective tissue; (4) cartilage; (5) bone.
"The physiological character of muscular tissue is contained in the increased capacity for