Fig. 4. Case of complete syndactyly in the foot. II and III, digit apparently representing the index and medius. c2 + c3, bone apparently representing the middle and external cuneiform; cb, cuboid; c1, internal cuneiform. (After Gruber.)
Webbing between the digits, in at least some of its manifestations, is a variation of similar nature. The family recorded by Newsholme[12] very clearly shows the dominance of this condition. The case is morphologically of great interest and must undoubtedly have a bearing on the problems of the mechanics of Division. In discussing the phenomena of syndactylism I pointed out some years ago that the digits most frequently united in the human hand are III and IV, while in the foot, union most frequently takes place between II and III.[13] In Newsholme's family the union was always between II and III of the foot, except in the case of one male who had the digits III and IV of the right hand alone webbed together. There can be little doubt that the geometrical system on which the foot is planned has an axis of symmetry passing between the digits II and III, while the corresponding axis in the hand passes between III and IV. Union between such digits may therefore be regarded as comparable with any non-division or "coalescence" of lateral structures in a middle line, and when as in these examples such a condition is shown to be a dominant we cannot avoid the inference that some concrete factor has the power of suppressing or inhibiting this division. Figs. 3 and 4 illustrate degrees of union between digits in the human hand and foot.
It is not in question that various other forms of irregular webbing and coalescence of digits exist, and respecting the genetic behaviour of these practically nothing is as yet known. Such a case is described by Walker,[14] in which the first and second metacarpals of both feet were fused in mother and daughter, and several more are found in literature. Contrasted with these phenomena we have the curious fact that in the Pigeon, Staples-Browne found webbing of the toes a recessive character. The question thus arises whether this webbing is of the same nature as that shown to be a dominant in Man, and indeed whether the phenomenon in pigeons is really meristic at all. There is some difference perceptible between the two conditions; for in Man there is not so much a development of a special web-like skin uniting the digits as a want of proper division between the digits themselves, and in extreme cases two digits may be represented by a single one. In the Pigeon I am not aware that a real union of this kind has ever been observed, and though the web-like skin may extend the whole length of the digits and be so narrow as to prevent the spread of the toes, it may, I think, be maintained that the unity of the digits is unimpaired. For the present the nature of this variation in the pigeon's feet must be regarded as doubtful, and we should note that if it is actually an example of a more perfect division being dominant to a less perfect division, the case is a marked exception to the general rule that non-division is dominant to division.
Reference must also be made to the phenomenon of fasciation in the stems of plants. As Mendel showed in the case of Pisum this condition is often a recessive. The appearances suggest that the difference between a normal and a fasciated plant consists in the inability of the fasciated plant to separate its lateral branches. The nature of the condition is however very obscure and it is equally likely that some multiplication of the growing point is the essential phenomenon.[15]
Stockard's interesting experiments[16] illustrate this question. He showed that by treating the embryos of a fish (Fundulus heteroclitus) with a dilute solution of magnesium salts, various cyclopian monstrosities were frequently produced. These have been called cases of fusion of the optic vesicles. I would prefer to regard them as cases of a division suppressed or restricted by the control of the environment. Conversely, the splendid discovery of Loeb, that an unfertilised egg will divide and develop parthenogenetically without fertilisation, as a consequence of exposure to various media, may be interpreted as suggesting that the action of those media releases the strains already present in the ovum, though I admit that an interpretation based on the converse hypothesis, that the medium acts as a stimulus, is as yet by no means excluded.
In these cases we come nearest to the direct causation or the direct inhibition of a division, but the meaning of the evidence is still ambiguous. I incline to compare Loeb's parthenogenesis with the development (and of course accompanying cell-division) of dormant buds on stems which have been cut back.
It is interesting to note that sometimes as an abnormality, the faculty of division gets out of hand and runs a course apparently uncontrolled. A remarkable instance of this condition is seen in Begonia "phyllomaniaca", which breaks out into buds at any point on the stem, petioles, or leaves, each bud having, like other buds, the power of becoming a new plant if removed. We would give much to know the genetic properties of B. phyllomaniaca, and in conjunction with Mr. W. O. Backhouse I have for some time been experimenting with this plant. It proved totally sterile. Its own anthers produce no pollen, and all attempts to fertilise it with other species failed though the pollen of a great number of forms was tried.
Recently however we have succeeded in making plants which are in every respect Begonia phyllomaniaca, so far as the characters of stems and leaves are concerned. These plants, of which we have sixteen, were made by fertilising B. heracleifolia with B. polyantha. They are all beginning to break out in "phyllomania." As yet they have not flowered, but as they agree in all details with phyllomaniaca there can be little doubt that the original plant bearing that name was a hybrid similarly produced. The production of "phyllomania" on a hybrid Begonia has also been previously recorded by Duchartre.[17] In this case the cross was made between B. incarnata and lucida. The synonymy of the last species is unfortunately obscure, and I have not succeeded in repeating the experiment.
