And let us add, to complete this summary of the constitution of cellular protoplasm, that it presents, at any rate at a certain moment, a remarkable organ, the centrosome, which plays an important part in cellular division. Its pre-existence is not certain. Some writers make it issue from the nucleus. At the moment of cellular division it appears like a compressed mass of granulations, which may be deeply stained. Around it is seen a clear unstainable zone, called the attraction-sphere; and finally, beyond this is a crown of striæ, which diverge like the rays of a halo—i.e., the aster. In conclusion, there are yet in the cellular body three kinds of non-essential bodies: the vacuoles, the leucites, and various inclusions. The vacuoles are cavities, some inert, some contractile; the leucites are organs for the manufacture of particular substances; the inclusions are the manufactured products, or wastes.

The Nucleus.—Every cell capable of living, growing, and multiplying, possesses a nucleus of constitution very analogous to the cellular mass which surrounds it. The anatomical elements in which no nucleus is found, such as the red globules of blood in adult mammals, are bodies which are certain, sooner or later, to disappear. There is therefore no real cell without a nucleus, any more than there is a nucleus without a cell. The exceptions to this law are only apparent. Histologists have examined them one by one, and have shown their purely specious character. We may therefore lay aside, subject to possible appeal from this decision, organisms such as Haeckel’s monera and the problem of finding out if bacteria really have a nucleus. The very great, if not the absolute generality of the nuclear body, must be admitted.

It hence follows that there is a nuclear protoplasm and a nuclear juice, just as we have seen that there is a protoplasm and a cellular juice. What was just said of the one may now be repeated of the other, and perhaps with even more emphasis. The nuclear protoplasm is a filamentary mass sometimes formed of a single mitome or cord, folded over on itself and capable of being unrolled. The mitome in its turn is a string of microsomes united by the cement of the linin. These are the same constituent elements as before, and the language of science distinguishes them one from the other by a prefix to their name of the words cyto or karyo, which in Greek signify cell and nucleus, according as they belong to one or the other of these organs. These are mere matters of nomenclature, but we know that in the descriptive sciences such matters are not of minor importance.

We have just indicated that in a state of repose,—that is to say, under ordinary conditions,—the structure of a nucleus reproduces clearly the structure of the cellular protoplasm which surrounds it. The nuclear essence is best separated from the spongioplasm. It takes more clearly the form of a filamentary thread, and the filaments themselves (mitome) show very thick chromatic granulations, or microsomes, connected by the linin.

At the moment of reproduction of the cell these granulations blend into a stainable sheath which surrounds the filaments, and the latter dispose themselves so as to form a single thread. This chromatic filament, which has now become a single thread, is shortened as it thickens (spireme); it is then cut into segments, twelve or twenty-four in the case of animals and a larger number in the case of plants. These are chromosomes, or nuclear segments, or chromatic loops. Their part is a very important one. They are constant in number and permanent during the whole of the life of the cell. Let us add that the nucleus still contains accessory elements (nucleoli).

The Rôle of the Nucleus.—Experiment has shown that the nucleus presides over the nutrition, the growth, and the conservation of the cell. If, following the example of Balbiani, Gruber, Nussbaum, and W. Roux of Leipzig, we cut into two a cell without injuring the nucleus, the fragment which is denuded of the nucleus continues to perform its functions for some time in the ordinary manner, and in some measure in virtue of its former impulse. It then declines and dies. On the contrary, the fragment provided with the nucleus repairs its wound, is reconstituted and continues to live. Thus the nucleus takes a very remarkable part in the reproduction of the cell, but it is still a matter of uncertainty whether its rôle is here subordinated to that of the cellular body, or if it is pre-eminent. However that may be, it follows from this experiment that the nucleus presents all the characteristics of a vigorous vitality, and that it is in its protoplasm that the chemists should be able to find the compounds, the special albuminoids, which, par excellence, form living matter.

§ 3. The Physical Constitution of Living Matter. The Micellar Theory.

Physical Constitution of Living Matter.—Microscopic examination does not take us much farther. The microscope, with the strongest magnification of which it is capable at present, shows us nothing beyond these links of aligned microsomes forming the species of protoplasmic thread or mitome, whose cellular body is a confused tangle or a very tangled ball. It is not probable that direct sight can penetrate much farther than this. No doubt the microscope, which has been so vastly improved, is capable of still further improvement. But these improvements are not indefinite. We have already reached a linear magnification of 2000, and theory tells us that a magnification of 4000 is the limit which cannot be passed. The penetrating power of the instrument is therefore near its culminating point. It has already given almost all that we have a right to expect from it.

We must, however, penetrate beyond this microscopic structure at which the sense of sight has been arrested. How is this to be done? When observation is arrested, hypothesis takes its place. Here there are two kinds of hypotheses, the one purely anatomical, the other physical. Anatomically, beyond the visible microsomes there have been imagined invisible hyper-microscopic corpuscles, the plastidules of Haeckel, the idioblasts of Hertwig, the pangenes of de Vries, the plasomes of Wiesner, the gemmules of Darwin, and the biophores of Weismann.

Biologists who have not got all that they hoped from microscopic structure are therefore thrown back on hyper-microscopic structure.