On the other hand, however, I do not see that such is the case with respect to idants; and still less do I see any reason for identifying the latter with chromosomes—even assuming that chromosomes are the visible repositories of the carriers of heredity[35].
Referring the reader to Weismann’s own exposition for a full account of these and many other additions to his general theory of germ-plasm, I will at once proceed to consider the alterations or emendations of that theory which have been published in his last two volumes, and which, as we shall find, have in large measure anticipated some of the most important points in the foregoing criticism. Therefore in the following criticism I will consider seriatim what he has now said touching all these points, and conclude by offering some general remarks on the resulting position of his general system of theories up to the present date.
Pursuing the same method of criticism as that adopted in the preceding chapters, we will first consider the further modifications of Weismann’s theory of heredity, and next those of his theory of organic evolution.
Weismann’s theory of Heredity (1893).
First of all, Weismann has now profoundly modified his theory of polar bodies. For, owing to certain more recent researches of Professor O. Hertwig, he very candidly allows:—“My previous interpretation of the first polar body as the removal of ovogenetic nucleo-plasm from the egg must fall to the ground: about this there is no possible doubt[36].”
He now regards both polar bodies as concerned in the same function of removing superfluous germ-plasm. Therefore one-half of his previous theory is abandoned: “the ovogenetic idio-plasm” is now supposed to be simply absorbed in the course of ontogeny, as I had suggested in one of the preceding chapters (pp. 42-46). The consequence is that he has now nothing to oppose to the view which is likewise there suggested (pp. 43-44)—viz., that his whole theory of polar bodies is rendered needless and improbable by the fact that the very mode in which ova are produced renders ample provision for the removal of any amount of superfluous germ-plasm which the theory of germ-plasm may require.
It is needless to say, after what has already been said in the pages just referred to, that in my opinion Professor Weismann has improved his main system of theories by dropping this part of his subordinate and, for the most part, separate theory of polar bodies. I only wish he could have seen his way to dropping the whole.
Again, he has now fully considered the phenomena of repair, regeneration, reproduction from somatic tissues, budding, and graft-hybridization.
Touching the four former he takes the view which I have supposed that he would (p. 53). As regards the latter, he fully accepts the fact of an occasional transmission of characters from one species or variety of plant to another by mere grafting[37]. But, although the explanation which he gives of this fact may pass muster so far as the only case which he deals with in detail is concerned, I do not see how it can do so to many others. For the case which he considers is that of Cystisus adami, where a bud of one species of Laburnum having been inserted in the wood of another produced a shoot which presented intermediate characters; and these have ever since been propagated by cuttings. Weismann’s interpretation of the facts here is, “that they were due to an abnormal kind of amphimixis, so that the idants of both species were combined in the apical cell of the first shoot[38].” Now, although this explanation may well apply to a case of graft-hybridization by means of buds, it obviously cannot do so to any case where hybridization is produced by the grafting of woody tissues. For here there is no “apical cell” in the question; and therefore the difficulties which I have adduced on page 82 remain. Possibly Weismann may dispute the fact of hybridization in any of these cases; but, as he has not expressly done so, I will not go into the question of evidence[39].