But the living cell grows in a totally different way, very much as a piece of glue swells up in water, by “imbibition,” or by interpenetration into and throughout its entire substance. The semifluid colloid mass takes up water, partly to combine chemically with its individual molecules[267], partly by physical diffusion into the interstices between these molecules, and partly, as it would seem, in other ways; so that the entire phenomenon is a very complex and even an obscure one. But, so far as we are concerned, the net result is a very simple one. For the equilibrium or tendency to equilibrium of fluid pressure in all parts of its interior while the process of imbibition is going on, the constant rearrangement of its fluid mass, the contrast in short with the crystalline method of growth where each particle comes to rest to move (relatively to the whole) no more, lead the mass of jelly to swell up, very much as a bladder into which we blow air, and so, by a graded and harmonious distribution of forces, to assume everywhere a rounded and more or less bubble-like external form[268]. So, when the same school of older naturalists called attention to a new distinction or contrast of form between the organic and inorganic objects, in that the contours of the former tended to roundness and curvature, and those of the latter to be bounded by straight lines, planes and sharp angles, we see that this contrast was not a new and different one, but only another aspect of their former statement, and an immediate consequence of the difference between the processes of agglutination and intussusception.
This common and general contrast between the form of the crystal on the one hand, and of the colloid or of the organism on the other, must by no means be pressed too far. For Lehmann, {204} in his great work on so-called Fluid Crystals[269], to which we shall afterwards return, has shewn how, under certain circumstances, surface-tension phenomena may coexist with crystallisation, and produce a form of minimal potential which is a resultant of both: the fact being that the bonds maintaining the crystalline arrangement are now so much looser than in the solid condition that the tendency to least total surface-area is capable of being satisfied. Thus the phenomenon of “liquid crystallisation” does not destroy the distinction between crystalline and colloidal forms, but gives added unity and continuity to the whole series of phenomena[270]. Lehmann has also demonstrated phenomena within the crystal, known for instance as transcrystallisation, which shew us that we must not speak unguardedly of the growth of crystals as limited to deposition upon a surface, and Bütschli has already pointed out the possible great importance to the biologist of the various phenomena which Lehmann has described[271].
So far then, as growth goes on, unaffected by pressure or other external force, the fluidity of protoplasm, its mobility internal and external, and the manner in which particles move with comparative freedom from place to place within, all manifestly tend to the production of swelling, rounded surfaces, and to their great predominance over plane surfaces in the contour of the organism. These rounded contours will tend to be preserved, for a while, in the case of naked protoplasm by its viscosity, and in the presence of a cell-wall by its very lack of fluidity. In a general way, the presence of curved boundary surfaces will be especially obvious in the unicellular organisms, and still more generally in the external forms of all organisms; and wherever mutual pressure between adjacent cells, or other adjacent parts, has not come into play to flatten the rounded surfaces into planes.
But the rounded contours that are assumed and exhibited by {205} a piece of hard glue, when we throw it into water and see it expand as it sucks the water up, are not nearly so regular or so beautiful as are those which appear when we blow a bubble, or form a drop, or pour water into a more or less elastic bag. For these curving contours depend upon the properties of the bag itself, of the film or membrane that contains the mobile gas, or that contains or bounds the mobile liquid mass. And hereby, in the case of the fluid or semifluid mass, we are introduced to the subject of surface tension: of which indeed we have spoken in the preceding chapter, but which we must now examine with greater care.
Among the forces which determine the forms of cells, whether they be solitary or arranged in contact with one another, this force of surface-tension is certainly of great, and is probably of paramount importance. But while we shall try to separate out the phenomena which are directly due to it, we must not forget that, in each particular case, the actual conformation which we study may be, and usually is, the more or less complex resultant of surface tension acting together with gravity, mechanical pressure, osmosis, or other physical forces.
Surface tension is that force by which we explain the form of a drop or of a bubble, of the surfaces external and internal of a “froth” or collocation of bubbles, and of many other things of like nature and in like circumstances[272]. It is a property of liquids (in the sense at least with which our subject is concerned), and it is manifested at or very near the surface, where the liquid comes into contact with another liquid, a solid or a gas. We note here that the term surface is to be interpreted in a wide sense; for wherever we have solid particles imbedded in a fluid, wherever we have a non-homogeneous fluid or semi-fluid such as a particle {206} of protoplasm, wherever we have the presence of “impurities,” as in a mass of molten metal, there we have always to bear in mind the existence of “surfaces” and of surface tensions, not only on the exterior of the mass but also throughout its interstices, wherever like meets unlike.
Surface tension is due to molecular force, to force that is to say arising from the action of one molecule upon another, and it is accordingly exerted throughout a small thickness of material, comparable to the range of the molecular forces. We imagine that within the interior of the liquid mass such molecular interactions negative one another: but that at and near the free surface, within a layer or film approximately equal to the range of the molecular force, there must be a lack of such equilibrium and consequently a manifestation of force.
The action of the molecular forces has been variously explained. But one simple explanation (or mode of statement) is that the molecules of the surface layer (whose thickness is definite and constant) are being constantly attracted into the interior by those which are more deeply situated, and that consequently, as molecules keep quitting the surface for the interior, the bulk of the latter increases while the surface diminishes; and the process continues till the surface itself has become a minimum, the surface-shrinkage exhibiting itself as a surface-tension. This is a sufficient description of the phenomenon in cases where a portion of liquid is subject to no other than its own molecular forces, and (since the sphere has, of all solids, the smallest surface for a given volume) it accounts for the spherical form of the raindrop, of the grain of shot, or of the living cell in many simple organisms. It accounts also, as we shall presently see, for a great number of much more complicated forms, manifested under less simple conditions.
Let us here briefly note that surface tension is, in itself, a comparatively small force, and easily measurable: for instance that of water is equivalent to but a few grains per linear inch, or a few grammes per metre. But this small tension, when it exists in a curved surface of very great curvature, gives rise to a very great pressure directed towards the centre of curvature. We can easily calculate this pressure, and so satisfy ourselves that, when the radius of curvature is of molecular dimensions, the {207} pressure is of the magnitude of thousands of atmospheres,—a conclusion which is supported by other physical considerations.