The Principles of Biology Vol. I/Chapter II.2a
CHAPTER IIA.
STRUCTURE.[1]
§ 54a. As, in the course of evolution, we rise from the smallest to the largest aggregates by a process of integration, so do we rise by a process of differentiation from the simplest to the most complex aggregates. The initial types of life are at once extremely small and almost structureless. Passing over those which swarm in the air, the water, and the soil, and are now some of them found to be causes of diseases, we may set out with those ordinarily called Protozoa and Protophyta: the lowest of which, however, are either at once plants and animals, or are now one and now the other.
That the first living things were minute portions of simple protoplasm is implied by the general theory of Evolution; but we have no evidence that such portions exist now. Even admitting that there are protoplasts (using this word to include plant and animal types) which are without nuclei, still they are not homogeneous—they are granular. Whether a nucleus is always present is a question still undecided; but in any case the types from which it is absent are extremely exceptional. Thus the most general structural traits of protoplasts are—the possession of an internal part, morphologically central though often not centrally situated, a general mass of protoplasm surrounding it, and an inclosing differentiated portion in contact with the environment. These essential elements are severally subject to various complications.
In some simple types the limiting layer or cortical substance can scarcely be said to exist as a separate element. The exoplasm, distinguished from the endoplasm by absence or paucity of granules, is continually changing places with it by the sending out of pseudopodia which are presently drawn back into the general mass: the inner and outer, being unsettled in position, are not permanently differentiated. Then we have types, exemplified by Lithamœba, constituted of protoplasm covered by a distinct pellicle, which in sundry groups becomes an outer shell of various structure: now jelly-like, now of cellulose, now siliceous or calcareous. While here this envelope has a single opening, there it is perforated all over—a fenestrated shell. In some cases an external layer is formed of agglutinated sand-particles; in others of imbricated plates, as in Coccospheres; and in many others radiating spicules stand out on all sides. Throughout sundry classes the exoplasm develops cilia, by the wavings of which the creatures are propelled through the water—cilia which may be either general or local. And then this cortical layer, instead of being spherical or spheroidal, may become plano-spiral, cyclical, crosier-shaped, and often many-chambered; whence there is a transition to colonies.
Meanwhile the inclosed protoplasm, at first little more than a network or foamwork containing granules and made irregular by objects drawn in as nutriment, becomes variously complicated. In some low types its continuity is broken by motionless, vacant spaces, but in higher types there are contractile vacuoles slowly pulsing, and, as we may suppose, moving the contained liquid hither and thither; while there are types having many passive vacuoles along with a few active ones. In some varieties the protruded parts, or pseudopodia, into which the protoplasm continually shapes itself, are comparatively short and club-shaped; in others they are long and fine filaments which anastomose, so forming a network running here and there into little pools of protoplasm. Then there are kinds in which the protoplasm streams up and down the protruding spicules: sometimes inside of them, sometimes outside. Always, too, there is included in the protoplasm a small body known as a centrosome.
Lastly, we have the innermost element, considered the essential element—the nucleus. According to Prof. Lankester, it is absent from Archerina, and there are types in which it is made visible only by the aid of special reagents. Ordinarily it is marked off from the surrounding protoplasm by a delicate membrane, just as the protoplasm itself is marked off by the exoplasm from the environment. Most commonly there is a single nucleus, but occasionally there are many, and sometimes there is a chief one with minor ones. Moreover, within the nucleus itself there have of late years been discovered remarkable structural elements which undergo complicated changes.
These brief statements indicate only the most general traits of an immense variety of structures—so immense a variety that Prof. Lankester, in distinguishing the classes, sub-classes, orders, and genera in the briefest way, occupies 37 quarto pages of small type. And to give a corresponding account of Protophyta would require probably something like equal space. Thus these living things, so minute that unaided vision fails to disclose them, constitute a world exhibiting varieties of structure which it requires the devotion of a life to become fully acquainted with.
§ 54b. If higher forms of life have arisen from lower forms by evolution, the implication is that there must once have existed, if there do not still exist, transitional forms; and there follows the comment that there do still exist transitional forms. Both in the plant-world and in the animal-world there are types in which we see little more than simple assemblages of Protophyta or of Protozoa—types in which the units, though coherent, are not differentiated but constitute a uniform mass. In treating of structure we are not here concerned with these unstructured types, but may pass on to those aggregates of protoplasts which show us differentiated parts—Metaphyta and Metazoa: economizing space by limiting our attention chiefly to the last.
When, half a century ago, some currency was given to the statement that all kinds of organisms, plant and animal, which our unaided eyes disclose, are severally composed of myriads of living units, some of them partially, if not completely, independent, and that thus a man is a vast nation of minute individuals of which some are relatively passive and others relatively active, the statement met, here with incredulity and there with a shudder. But what was then thought a preposterous assertion has now come to be an accepted truth.
Along with gradual establishment of this truth has gone gradual modification in the form under which it was originally asserted. If some inhabitant of another sphere were to describe one of our towns as composed exclusively of houses, saying nothing of the contained beings who had built them and lived in them, we should say that he had made a profound error in recognizing only the inanimate elements of the town and disregarding the animate elements. Early histologists made an analogous error. Plants and animals were found to consist of minute members, each of which appeared to be simply a wall inclosing a cavity—a cell. But further investigation proved that the content of the cell, presently distinguished as protoplasm, is its essential living part, and that the cell-wall, when present, is produced by it. Thus the unit of composition is a protoplast, usually enclosed, with its contained nucleus and centrosome.
§ 54c. As above implied, the individualities of the units are not wholly lost in the individuality of the aggregate, but continue, some of them, to be displayed in various degrees: the great majority of them losing their individualities more and more as the type of the aggregate becomes higher.
In a slightly organized Metazoon like the sponge, the subordination is but small. Only those members of the aggregate which, flattened and united together, form the outer layer and those which become metamorphosed into spicules, have entirely lost their original activities. Of the rest nearly all, lining the channels which permeate the mass, and driving onwards the contained sea-water by the motions of their whip-like appendages, substantially retain their separate lives; and beyond these there exist in the gelatinous substance lying between the inner and outer layers, which is regarded as homologous with a mesoderm, amœba-form protoplasts which move about from place to place.
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;—
"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 contraction.
"The morphological character is found in the fact that the cells have secreted muscle-substance.
"According to the nature of the muscle-substance are distinguished smooth and cross-striated muscle-fibres.
"According to the character and derivation of the cells (muscle-corpuscles) the musculature is divided into epithelial (epithelial muscle-cells, primary bundles) and connective-tissue muscle cells (contractile fibre-cells).
"The physiological character of nervous tissue rests upon the transmission of sensory stimuli and voluntary impulses, and upon the co-ordination of these into unified psychic activity.
"The conduction takes place by means of nerve-fibres (non-medullated and medullated fibrils and bundles of fibrils); the co-ordination of stimuli by means of ganglion-cells (bipolar, multipolar ganglion-cells)." (General Principles of Zoology, pp. 117-8.)But now concerning cells out of which, variously modified, obscured, and sometimes obliterated, tissues are formed, we have to note a fact of much significance. Along with the cell-doctrine as at first held, when attention was given to the cell itself rather than to its contents, there went the belief that each of these morphological units is structurally separate from its neighbours. But since establishment of the modern view that the essential element is the contained protoplasm, histologists have discovered that there are protoplasmic connexions between the contents of adjacent cells. Though cursorily observed at earlier dates, it was not until some twenty years ago that in plant-tissues these were clearly shown to pass through openings in the cell-walls. It is said that in some cases the openings are made, and the junctions established, by a secondary process; but the implication is that usually these living links are left between multiplying protoplasts; so that from the outset the protoplasm pervading the whole plant maintains its continuity. More recently sundry zoologists have alleged that a like continuity exists in animals. Especially has this been maintained by Mr. Adam Sedgwick. Numerous observations made on developing ova of fishes have led him to assert that in no case do the multiplying cells so-called—blastomeres and their progeny—become entirely separate. Their fission is in all cases incomplete. A like continuity has been found in the embryos of many Arthropods, and more recently in the segmenting eggs and blastulæ of Echinoderms. The syncytium thus formed is held by Mr. Sedgwick to be maintained in adult life, and in this belief he is in agreement with sundry others. Bridges of protoplasm have been seen between epithelium-cells, and it is maintained that cartilage-cells, connective tissue cells, the cells forming muscle-fibres, as well as nerve-cells, have protoplasmic unions. Nay, some even assert that an ovum preserves a protoplasmic connexion with the matrix in which it develops.
A corollary of great significance may here be drawn. It has been observed that within a vegetal cell the strands of protoplasm stretched in this or that direction contain moving granules, showing that the strands carry currents. It has also been observed that when the fission of a protozoon is so nearly complete that its two halves remain connected only by a thread, currents of protoplasm move through this thread, now one way now the other. The inference fairly to be drawn is that such currents pass also through the strands which unite the protoplasts forming a tissue. What must happen? So long as adjacent cells with their contents are subject to equal pressures no tendency to redistribution of the protoplasm exists, and there may then occur the action sometimes observed inside the strands within a cell: currents with their contained granules moving in opposite directions. But if the cells forming a portion of tissue are subject to greater pressure than the cells around, their contained protoplasm must be forced through the connecting threads into these surrounding cells. Every change of pressure at every point must cause movements and counter-movements of this kind. Now in the Metazoa at large, or at least in all exhibiting relative motions of parts, and especially in all which are capable of rapid locomotion, such changes of pressure are everywhere and always taking place. The contraction of a muscle, besides compressing its components, compresses neighbouring tissues; and every instant contractions and relaxations of muscles go on throughout the limbs and body during active exertion. Moreover, each attitude—standing, sitting, lying down, turning over—entails a different set of pressures, both of the parts on one another and on the ground; and those partial arrests of motion which result from sitting down the feet alternately when running, send jolts or waves of varying pressure through the body. The vital actions, too, have kindred effects. An inspiration alters the stress on the tissues throughout a considerable part of the trunk, and a heart-beat propels, down to the smallest arteries, waves which slightly strain the tissues at large. The component cells, thus subject to mechanical disturbances, small and great, perpetual and occasional, are ever having protoplasm forced into them and forced out of them. There are gurgitations and regurgitations which, if they do not constitute a circulation properly so called, at least imply an unceasing redistribution. And the implication is that in the course of days, weeks, months, years, each portion of protoplasm visits every part of the body.
Without here stating specifically the bearings of these inferences upon the problems of heredity, it will be manifest that certain difficulties they present are in a considerable degree diminished.
§ 54e. Returning from this parenthetical discussion to the subject of structure, we have to observe that besides facts presented by tissues and facts presented by organs, there are certain facts, less general than the one and more general than the other, which must now be noted. In the order of decreasing generality an account of organs should be preceded by an account of systems of organs. Some of these, as the muscular system and the osseous system, are co-extensive with tissues, but others of them are not. The nervous system, for example, contains more than one kind of tissue and is constituted of many different structures: besides afferent and efferent nerves there are the ganglia immediately controlling the viscera, and there are the spinal and cerebral masses, the last of which is divisible into numerous unlike parts. Then we have the vascular system made up of the heart, arteries, veins, and capillaries. The lymphatic system, too, with its scattered glands and ramifying channels has to be named. And then, not forgetting the respiratory system with its ancillary appliances, we have the highly heterogeneous alimentary system; including a great number of variously-constructed organs which work together. On contemplating these systems we see their common character to be that while as wholes they cooperate for the carrying on of the total life, each of them consists of cooperative parts: there is cooperation within cooperation.
There is another general aspect under which structures must be contemplated. They are divisible into the universal and the particular—those which are everywhere present and those which occupy special places. The blood which a scratch brings out shows us that the vascular system sends branches into each spot. The sensation accompanying a scratch proves that the nervous system, too, has there some of its ultimate fibrils. Unobtrusive, and yet to be found at every point, are the ducts of the lymphatic system. And in all parts exists the connective tissue—an inert tough substance which, running through interspaces, wraps up and binds together the other tissues. As is implied by this description, these structures stand in contrast with local structures. Here is a bone, there is a muscle, in this place a gland, in that a sense-organ. Each has a limited extent and a particular duty. But through every one of them ramify branches of these universal structures. Every one of them has its arteries and veins and capillaries, its nerves, its lymphatics, its connective tissue.
Recognition of this truth introduces what little has here to be said concerning organs; for of course in a work limited to principles no detailed account of these can be entered upon. This remainder truth is that, different as they may be in the rest of their structures, all organs are alike in certain of their structures. All are furnished with these appliances for nutrition, depuration and excitation: they have all to be sustained, all to be stimulated, all to be kept clean. It has finally to be remarked that the general structures which pervade all the special structures at the same time pervade one another. The universal nervous system has everywhere ramifying through it the universal vascular system which feeds it; and the universal vascular system is followed throughout all its ramifications by special nerves which control it. The lymphatics forming a drainage-system run throughout the other systems; and in each of these universal systems is present the connective tissue holding their parts in position.
§ 54f. So vast and varied a subject as organic structure, even though the treatment of it is limited to the enunciation of principles, cannot, of course, be dealt with in the space here assigned. Next to nothing has been said about plant-structures, and in setting forth the leading traits of animal-structures the illustrations given have been mostly taken from highly-developed creatures. In large measure adumbration rather than exposition is the descriptive word to be applied.
Nevertheless the reader may carry away certain truths which, exemplified in a few cases, are exemplified more or less fully in all cases. There is the fundamental fact that the plants and animals with which we are familiar—Metaphyta and Metazoa—are formed by the aggregation of units homologous with Protozoa. These units, often conspicuously showing their homology in early embryonic stages, continue some of them to show it throughout the lives of the highest type of Metazoa, which contain billions of units carrying on a protozoon life. Of the protoplasts not thus active the great mass, comparatively little transformed in low organisms, become more and more transformed as the ascent to high organisms goes on; so that, undergoing numerous kinds of metamorphoses, they lose all likeness to their free homologues, both in shape and composition. The cell-contained protoplasts thus variously changed are fused together into tissues in which their individualities are practically lost; but they nevertheless remain connected throughout by permeable strands of protoplasm. Arising by complication of the outer and inner layers of the embryo and growing more unlike as their units become more obscured, these tissues are formed into systems, which develop into sets of organs. Some of the resulting structures are localized and special but others are everywhere interfused.
While the first named of these facts are displayed in every Metazoon, and while the last named are visible only in Metazoa of considerably developed structures, a gradual transition is shown in intermediate kinds of Metazoa. Of this transition it remains to say that it is effected by the progressive development of auxiliary appliances. For example, the primitive foot-cavity is a sac with one opening only; then comes a second opening through which the waste-matter of the food is expelled. The alimentary canal between these openings is at first practically uniform; afterwards in a certain part of its wall arise numerous bile-cells; these accumulating form a hollow prominence; and this, enlarging, becomes in higher types a liver, while the hollow becomes its duct. In other gradual ways are formed other appended glands. Meanwhile the canal itself has its parts differentiated: one being limited to swallowing, another to triturating, another to adding various solvents, another to absorbing the prepared nutriment, another to ejecting the residue. Take again the visual organ. The earliest form of it is a mere pigment-speck below the surface. From this (saying nothing here of multiple eyes) we rise by successive complications to a retina formed of multitudinous sensory elements, lenses for throwing images upon it, a curtain for shutting out more or less light, muscles for moving the apparatus about, others for adjusting its focus; and, finally, added to these, either a nictitating membrane or eyelids for perpetually wiping its surface, and a set of eyelashes giving notice when a foreign body is dangerously near. This process of elaborating organs so as to meet additional requirements by additional parts, is the process pursued throughout the body at large.
Of plant-structures, concerning which so little has been said, it may here be remarked that their relative simplicity is due to the simplicity of their relations to food. The food of plants is universally distributed, while that of animals is dispersed. The immediate consequences are that in the one case motion and locomotion are superfluous, while in the other case they are necessary: the differences in the degrees of structure being consequences. Recognizing the locomotive powers of minute Algæ and the motions of such other Algæ as Oscillatoria, as well as those movements of leaves and fructifying organs seen in some Phænogams, we may say, generally, that plants are motionless; but that they can nevertheless carry on their lives because they are bathed by the required nutriment in the air and in the soil. Contrariwise, the nutriment animals require is distributed through space in portions: in some cases near one another and in other cases wide apart. Hence motion and locomotion are necessitated; and the implication is that animals must have organs which render them possible. In the first place there must be either limbs or such structures as those which in fish, snakes, and worms move the body along. In the second place, since action implies waste, there must be a set of channels to bring repairing materials to the moving parts. In the third place there must be an alimentary system for taking in and preparing these materials. In the fourth place there must be organs for separating and excreting waste-products. All these appliances must be more highly developed in proportion as the required activity is greater. Then there must be an apparatus for directing the motions and locomotions—a nervous system; and as fast as these become rapid and complex the nervous system must be largely developed, ending in great nervous centres—seats of intelligence by which the activities at large are regulated. Lastly, underlying all the structural contrasts between plants and animals thus originating, there is the chemical contrast; since the necessity for that highly nitrogenous matter of which animals are formed, is entailed by the necessity for rapidly evolving the energy producing motion. So that, strange as it seems, those chemical, physical, and mental characters of animals which so profoundly distinguish them from plants, are all remote results of the circumstance that their food is dispersed instead of being everywhere present.
- ↑ When, in 1863, the preceding chapter was written, it had not occurred to me that there needed an accompanying chapter treating of Structure. The gap left by that oversight I now fill up. In doing this there have been included certain statements which are tacitly presupposed in the last chapter, and there may also be some which overlap statements in the next chapter. I have not thought it needful so to alter adjacent chapters as to remove these slight defects: the duplicated ideas will bear re-emphasizing.