LITMIR.BIZ

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we can conceive that the human mind may at some time be capable of understanding it. We may at least maintain that it has been rendered intelligible, for we can thus trace heredity back to growth; we can thus look upon reproduction as an overgrowth of the individual, and can thus distinguish between a succession of species and a succession of individuals, because in the latter succession the germ-plasm remains similar, while in the succession of the former it becomes different. Thus individuals, as they arise, are always assuming new and more complex forms, until the interval between the simple unicellular protozoon and the most complex of all organisms—man himself—is bridged over.

      I have not been able to throw light upon all sides of the question which we are here discussing. There are still some essential points which I must leave for the present; and, furthermore, I am not yet in a position to explain satisfactorily all the details which arise at every step of the argument. But it appeared to me to be necessary to state this weighty and fundamental question, and to formulate it concisely and definitely; for only in this way will it be possible to arrive at a true and lasting solution of the problem. We must however be clear on this point—that the understanding of the phenomena of heredity is only possible on the fundamental supposition of the continuity of the germ-plasm. The value of experiment in relation to this question is somewhat doubtful. A careful collection and arrangement of facts is far more likely to decide whether, and to what extent, the continuity of germ-plasm is reconcilable with the assumption of the transmission of acquired characters from the parent body to the germ, and from the germ to the body of the offspring. At present such transmission is neither proved as a fact, nor has its assumption been shown to be unquestionably necessary.

      III.

      LIFE AND DEATH.

      1883

      LIFE AND DEATH.

      PREFACE

      The following paper was first printed as an academic lecture in the summer of the present year (1883), with the title ‘Upon the Eternal Duration of Life’ (‘Über die Ewigkeit des Lebens’). In now bringing it before a larger public in an expanded and improved form, I have chosen a title which seemed to me to correspond better with the present contents of the paper.

      The stimulus which led to this biological investigation was given in a memoir by Götte, in which this author opposes views which I had previously expressed. Although such an origin has naturally caused my paper to take the form of a reply, my intention was not merely to controvert the views of my opponent, but rather—using those opposed views as a starting-point—to throw new light upon certain questions which demand consideration; to give additional support to thoughts which I have previously expressed, and to penetrate, if possible, more deeply into the problem of life and death.

      If, in making this attempt, the views of my opponent have been severely criticized, it will be acknowledged that the criticisms do not form the purpose of my paper, but only the means by which the way to a more correct understanding of the problems before us may be indicated.

A. W.

      Freiburg i. Breisgau,

      Oct. 18, 1883.

      III.

      LIFE AND DEATH

      In the previous essay, entitled ‘The Duration of Life,’ I have endeavoured to show that the limitation of life in single individuals by death is not, as has been hitherto assumed, an inevitable phenomenon, essential to the very nature of life itself; but that it is an adaptation which first appeared when, in consequence of a certain complexity of structure, an unending life became disadvantageous to the species. I pointed out that we could not speak of natural death among unicellular animals, for their growth has no termination which is comparable with death. The origin of new individuals is not connected with the death of the old; but increase by division takes place in such a way that the two parts into which an organism separates are exactly equivalent one to another, and neither of them is older or younger than the other. In this way countless numbers of individuals arise, each of which is as old as the species itself, while each possesses the capability of living on indefinitely, by means of division.

      I suggested that the Metazoa have lost this power of unending life by being constructed of numerous cells, and by the consequent division of labour which became established between the various cells of the body. Here also reproduction takes place by means of cell-division, but every cell does not possess the power of reproducing the whole organism. The cells of the organism are differentiated into two essentially different groups, the reproductive cells—ova or spermatozoa, and the somatic cells, or cells of the body, in the narrower sense. The immortality of the unicellular organism has only passed over to the former; the others must die, and since the body of the individual is chiefly composed of them, it must die also.

      I have endeavoured to explain this fact as an adaptation to the general conditions of life. In my opinion life became limited in its duration, not because it was contrary to its very nature to be unlimited, but because an unlimited persistence of the individual would be a luxury without a purpose. Among unicellular organisms natural death was impossible, because the reproductive cell and the individual were one and the same: among multicellular animals it was possible, and we see that it has arisen.

      Natural death appeared to me to be explicable on the principle of utility, as an adaptation.

      These opinions, to which I shall return in greater detail in a later part of this paper, have been opposed by Götte59, who does not attribute death to utility, but considers it to be a necessity inherent in life itself. He considers that it occurs not only in the Metazoa or multicellular animals, but also in unicellular forms of life, where it is represented by the process of encystment, which is to be regarded as the death of the individual. This encystment is a process of rejuvenescence, which, after a longer or shorter interval, interrupts multiplication by means of fission. According to Götte, this process of rejuvenescence consists in the dissolution of the specific structure of the individual, or in the retrogression of the individual to a form of organic matter which is no longer living but which is comparable to the yolk of an egg. This matter is, by means of its internal energy, and in consequence of the law of growth which is inherent in its constitution, enabled to give rise to a new individual of the same species. Furthermore, the process of rejuvenescence among unicellular beings corresponds to the formation of germs in the higher organisms. The phenomena of death were transmitted by heredity from the unicellular forms to the Metazoa when they arose. Death does not therefore appear for the first time in the Metazoa, but it is an extremely ancient process which ‘goes back to the first origin of organic beings’ (l. c., p. 81).

      It is obvious, from this short résumé, that Götte’s view is totally opposed to mine. Inasmuch as only one of these views can be fundamentally right, it is worth while to compare the two; and although we cannot at present hope to explain the ultimate physiological processes which involve life and death, I think nevertheless that it is quite possible to arrive at definite conclusions as to the general causes of these phenomena. At any rate, existing facts have not been so completely thought out that it is useless to consider them once more.

      The question—what do we understand by death? must be decided before we can speak of the origin of death. Götte says, ‘we are not able to explain this general expression quite definitely and in all its details, because the moment of death, or perhaps more exactly the moment when death is complete, can in no case be precisely indicated. We can only say that in the death of the higher animals, all those phenomena which make up the life of the individual cease, and further that all the cells and elements of tissue which form the dead organism, die, and are resolved into their elements.’

      This definition would suffice if it did not include that which is to be defined. For it assumes that under the expression ‘dead organism’ we must include those organisms which have brought to an end the whole of their vital functions, but of which the component cells and elements may still be living. This view is afterwards more accurately explained, and in fact there is no doubt that the cessation of the activity of life in the multicellular organism rarely implies any direct connection with the cessation of vital functions in all its constituents. The question however arises,

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