Beyond this point studies upon the Orthopteran cells will not permit me to go; but Montgomery has been fortunate enough to find in Peripatus an object in which he considers it possible to demonstrate the continuity of the chromosomes from one generation to another, and their fusion by pairs in the early history of the spermatocyte to bring about the reduced number. This is, in the main, a logical conclusion to my own work, and I am therefore bound to regard his results as probably correct. While doing this, however, I recognize that the absolute proof he brings forward in support of his hypothesis is very slight. I consider any deductions based upon observations of linin structures as very insecure, and it is upon these that Montgomery principally relies to demonstrate his theory. Further observations upon the behavior of the chromosomes between the spermatogonia and the spermatocytes in objects favorable for study will be awaited with interest. In the meantime it must be conceded that the work upon insect spermatogenesis has at least lent strong support to the theory of the individuality of the chromosomes in general and has definitely shown that there is such a thing in some instances.

(g) Nucleoli.

Considerable importance is attached by some investigators to the nuclear structures, properly called plasmasomes, that occur in the spermatocytes. It is probable that there are marked differences between the cells of various species in regard to the occurrence of these bodies, for in the Orthoptera they either do not appear at all, or, if present, they are minute and inconspicuous. This fact would tend to disprove any theory which would attach a fundamental importance to these structures, such as is conceived for the chromatin. The Orthopteran cells do not allow any observations which would add to our positive knowledge of the nucleoli, and I include this brief statement merely for the negative value it may possess.

(h) Rest Stage.

In his first paper upon Euchistus, Montgomery assigns an important and conspicuous place to the “rest stage” among his numerous subphases preceding the first spermatocyte mitosis. As a result of his later comparative work upon the Hemiptera, however, we learn that in certain families no trace of such a condition of diffusion on the part of the chromatin is observable, from which we conclude that “accordingly such a stage would appear to have no broad significance.” It has already been announced that nothing like a rest stage intervenes between the spermatogonia and spermatocytes of the Orthoptera, and the work of most investigators would tend to indicate that it is the exception rather than the rule. In those cases where such a condition of the nucleus exists, it would seem to be true that nothing more unusual than an excessive diffusion of the spermatogonial chromosomes occurs, and this is of hardly sufficient importance to receive a special designation.

The existence of a rest stage between the first and second spermatocytes is also negatived by the conditions found in the Orthopteran cells. The formation of chromosomes in the prophase of the first spermatocyte that are already prepared for two divisions would a priori render improbable the intervention of a rest stage here; and the actual observed persistence of the chromosomes, as such, through the telophase of the first spermatocyte and through the modified prophase of the second spermatocyte gives actual proof in support of the view that commonly prevails regarding the suppression of the second spermatocyte rest stage.

Observations upon numerous species tend to show that the behavior of the chromatin during the period between the two spermatocyte mitoses varies considerably with the species and even within the species itself. The amount of diffusion would, in some measure, seem to be related to the form of the chromosomes and to vary correspondingly in those individuals where the chromosomes are of diverse forms. Thus, where the elements of the second spermatocyte metaphase appear as short double rods, the amount of diffusion is slight, and the individual chromosomes may be distinguished throughout the telophase of the first spermatocyte; but in those cases where the members of the mitotic figure are much elongated the diffusion is more extensive and the distinction between elements is made difficult or impossible. Since these two conditions may prevail in the same testis, it is probably only a question as to the extent of elongation on the part of each chromosome. In those cases where the elements become very much extended the appearance of the resting condition would be simulated closely, while, on the contrary, chromosomes consisting of spherical or short cylindrical chromatids would never give a suggestion of such a stage. In this we may find, I think, an explanation for those cases in which a rest stage is described as occurring between the spermatocyte generations.

VI. SUMMARY.

1. The secondary spermatogonia are much reduced in size at the end of their divisions and the cytoplasm is very small in amount. The rod-shaped chromosomes number thirty-three, and, of these, one is to be distinguished from its fellows by greater size and slower division.

2. From the substance of the disintegrated spermatogonial chromosomes, the tetrads of the first spermatocytes are formed. It was impossible to determine the relation of the elements of the two generations, but the changes are rapid and there is no intervening resting condition of the nucleus.