-shaped curvature (Fig. [143], D).
As a matter of fact, while we have abundant simple illustrations of the principles which we have now begun to study, apparent exceptions to this simplicity, due to an asymmetry of the cell itself, or of the system of which the single cell is but a part, are by no means rare. For example, we know that in cambium-cells, division frequently takes place parallel to the long axis of the cell, when a partition of much less area would suffice if it were set cross-ways: and it is only when a considerable disproportion has been set up between the length and breadth of the cell, that the balance is in part redressed by the appearance of a transverse partition. It was owing to such exceptions that Berthold was led to qualify and even to depreciate the importance of the law of minimal areas as a factor in cell-division, after he himself had done so much to demonstrate and elucidate it[390]. He was deeply and rightly impressed by the fact that other forces besides surface {358} tension, both external and internal to the cell, play their part in the determination of its partitions, and that the answer to our problem is not to be given in a word. How fundamentally important it is, however, in spite of all conflicting tendencies and apparent exceptions, we shall see better and better as we proceed.
But let us leave the exceptions and return to a consideration of the simpler and more general phenomena. And in so doing, let us leave the case of the cubical, quadrangular or cylindrical cell, and examine the case of a spherical cell and of its successive divisions, or the still simpler case of a circular, discoidal cell.
When we attempt to investigate mathematically the position and form of a partition of minimal area, it is plain that we shall be dealing with comparatively simple cases wherever even one dimension of the cell is much less than the other two. Where two dimensions are small compared with the third, as in a thin cylindrical filament like that of Spirogyra, we have the problem at its simplest; for it is at once obvious, then, that the partition must lie transversely to the long axis of the thread. But even where one dimension only is relatively small, as for instance in a flattened plate, our problem is so far simplified that we see at once that the partition cannot be parallel to the extended plane, but must cut the cell, somehow, at right angles to that plane. In short, the problem of dividing a much flattened solid becomes identical with that of dividing a simple surface of the same form.
There are a number of small Algae, growing in the form of small flattened discs, consisting (for a time at any rate) of but a single layer of cells, which, as Berthold shewed, exemplify this comparatively simple problem; and we shall find presently that it is also admirably illustrated in the cell-divisions which occur in the egg of a frog or a sea-urchin, when the egg for the sake of experiment is flattened out under artificial pressure.
Fig. 144. Development of Erythrotrichia. (After Berthold.)
Fig. [144] (taken from Berthold’s Monograph of the Naples Bangiaciae) represents younger and older discs of the little alga Erythrotrichia discigera; and it will be seen that, in all stages save the first, we have an arrangement of cell-partitions which looks somewhat complex, but into which we must attempt to throw some light and order. Starting with the original single, and flattened, {359} cell, we have no difficulty with the first two cell-divisions; for we know that no bisecting partitions can possibly be shorter than the two diameters, which divide the cell into halves and into quarters. We have only to remember that, for the sum total of partitions to be a minimum, three only must meet in a point; and therefore, the four quadrantal walls must shift a little, producing the usual little median partition, or cross-furrow, instead of one common, central point of junction. This little intermediate wall, however, will be very small, and to all intents and purposes