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Note 7. Bees

It has not been experimentally determined whether the workers, which are usually killed after some months, would live as long as the queen, if they were artificially protected from danger in the hive; but I think that this is probable, because it is the case among ants, and because the peculiarity of longevity must be latent in the egg. As is well known, the egg which gives rise to the queen is identical with that which produces a worker, and differences in the nutrition alone decide whether a queen or a worker shall be formed. It is therefore probable that the duration of life in queen and worker is potentially the same.

Note 8. Death of the Cells in higher Organisms

The opinion has been often expressed that the inevitable appearance of normal ‘death’ is dependent on the wearing out of the tissues in consequence of their functional activity. Bertin says, referring to animal life²⁵:—‘L’observation des faits y attache l’idée d’une terminaison fatale, bien que la raison ne découvre nullement les motifs de cette nécessité. Chez les êtres qui font partie du règne animal l’exercise même de la rénovation moléculaire finit par user le principe qui l’entretient sans doute parceque le travail d’échange ne s’accomplissant pas avec une perfection mathématique, il s’établit dans la figure, comme dans la substance de l’être vivant, une déviation insensible, et que l’accumulation des écarts finit par amener un type chimique ou morphologique incompatible avec la persistance de ce travail.’

Here the replacement of the used-up elements of tissue by new ones is not taken into account, but an attempt is made to show that the functions of the whole organism necessarily cause it to waste away. But the question at once arises, whether such a result does not depend upon the fact that the single histological elements,—the cells,—are worn out by the exercise of function. Bertin admits this to be the case, and this idea of the importance of changes in the cells themselves is everywhere gaining ground. But although we must admit that the histological elements do, as a matter of fact, wear out, in multicellular animals, this would not prove that, nor explain why, such changes must follow from the nature of the cell and the vital processes which take place within it. Such an admission would merely suggest the question:—how is it that the cells in the tissues of higher animals are worn out by their function, while cells which exist in the form of free and independent organisms possess the power of living for ever? Why should not the cells of any tissue, of which the equilibrium is momentarily disturbed by metabolism, be again restored, so that the same cells continue to perform their functions for ever:—why cannot they live without their properties suffering alteration? I have not sufficiently touched upon this point in the text, and as it is obviously important it demands further consideration.

In the first place, I think we may conclude with certainty from the unending duration of unicellular organisms, that such wearing out of tissue cells is a secondary adaptation, that the death of the cell, like general death, has arisen with the complex, higher organisms. Waste does not depend upon the intrinsic nature of the cells, as the primitive organisms prove to us, but it has appeared as an adaptation of the cells to the new conditions by which they are surrounded when they come into combination, and thus form the cell-republic of the metazoan body. The replacement of cells in the tissues must be more advantageous for the functions of the whole organism than the unlimited activity of the same cells, inasmuch as the power of single cells would be much increased by this means. In certain cases, these advantages are obvious, as for example in many glands of which the secretions are made up of cast-off cells. Such cells must die and be separated from the organism, or the secretion would come to an end. In many cases, however, the facts are obscure, and await physiological investigation. But in the meantime we may draw some conclusions from the effects of growth, which are necessarily bound up with a certain rate of production of new cells. In the process of growth a certain degree of choice between the old cells which have performed their functions up to any particular time, and the new ones which have appeared between them, is as it were left to the organism.

The organism may thus, figuratively speaking, venture to demand from the various specific cells of tissues a greater amount of work than they are able to bear, during the normal length of their life, and with the normal amount of their strength. The advantages gained by the whole organism might more than compensate for the disadvantages which follow from the disappearance of single cells. The glandular secretions which are composed of cell-detritus, prove that the cells of a complex organism may acquire functions which result in the loosening of their connexion with the living cell-community of the body, and their final separation from it. And the same facts hold with the blood corpuscles, for the exercise of their function results in ultimate dissolution. Hence it is not only conceivable, but in every way probable, that many other functions in the higher organisms involve the death of the cells which perform them, not because the living cell is necessarily worn out and finally killed by the exercise of any ordinary vital process, but because the specific functions in the economy of the cell community which such cells undertake to perform, involve the death of the cells themselves. But the fact that such functions have appeared,—involving as they do the sacrifice of a great number of cells,—entirely depends upon the replacement of the old by newly formed cells, that is by the process of reproduction in cells²⁶.

We cannot a priori dispute the possibility of the existence of tissues in which the cells are not worn out by the performance of function, but such an occurrence appears to be improbable when we recollect that the cells of all tissues owe their constitution to a very far-reaching process of division of labour, which leaves them comparatively one-sided, and involves the loss of many properties of the unicellular, self-sufficient organism. At any rate we only know of potential immortality in the cells which constitute independent unicellular organisms, and the nature of these is such that they are continually undergoing a complete process of reformation.

If we did not find any replacement of cells in the higher organism, we should be induced to look upon death itself as the direct result of the division of labour among the cells, and to conclude that the specific cells of tissues have lost, as a consequence of the one-sided development of their activities, the power of unending life, which belongs to all independent primitive cells. We should argue that they could only perform their functions for a certain time, and would then die, and with them the organism whose life is dependent upon their activity. The longer they are occupied with the performance of special functions, the less completely do they carry out the phenomena of life, and hence they lead to the appearance of retrogressive changes. But the replacement of cells is certain in many tissues (in glands, blood, etc.), so that we can never seek a satisfactory explanation in the train of reasoning indicated above, but we must assume the existence of limits to the replacement of cells. In my opinion, we can find an explanation of this in the general relations of the single individual to its species, and to the whole of the external conditions of life; and this is the explanation which I have suggested and have attempted to work out in the text.

Note 9. Death by Sudden Shock

The most remarkable example of this kind of death known to me, is that of the male bees. It has been long known that the drone perishes while pairing, and it was usually believed that the queen bites it to death. Later observations have however shown that this is not the case, but that the male suddenly dies during copulation, and that the queen afterwards bites through the male intromittent organ, in order to free herself from the dead body. In this case death is obviously due to sudden excitement, for when the latter is artificially induced, death immediately follows. Von Berlepsch made some very interesting observations on this point, ‘If one catches a drone by the wings, during the nuptial flight, and holds it free in the air without touching any other part, the penis is protruded and the animal instantly dies, becoming motionless as though killed by a shock. The same thing happens if one gently stimulates the dorsal surface of the drone on a similar occasion. The male is in such an excited and irritable condition that the slightest muscular movement or disturbance causes the penis to be protruded²⁷.’ In this case death is caused by the so-called nervous shock. The humble-bees are not similarly constituted, for the male does not die after fertilizing the female, ‘but withdraws its penis and flies away.’ But the death of male bees, during pairing, must not be regarded as normal death. Experiment has shown that these insects can live for more than four months²⁸. They do not, as a matter of fact, generally live so long; for—although the workers do not, as was formerly believed, kill them after the fertilization of the queen, by direct means—they prevent them from eating the honey and drive them from the hive, so that they die of hunger²⁹.

We must also look upon death which immediately, or very quickly, follows upon the deposition of eggs as death by sudden shock. The females of certain species of Psychidae, when they reproduce sexually, may remain alive for more than a week waiting for a male: after fertilization, however, they lay their eggs and die, while the parthenogenetic females of the same species lay their eggs and die immediately after leaving the cocoon; so that while the former live for many days, the latter do not last for more than twenty-four hours. ‘The parthenogenetic form of Solenobia triquetrella, soon after emergence, lays all her eggs together in the empty case, becomes much shrunken, and dies in a few hours.’ (Letter from Dr. Speyer, Rhoden.)

Note 10. Intermingling during the Fission of Unicellular Organisms³⁰

Fission is quite symmetrical in Amoebae, so that it is impossible to recognise mother and daughter in the two resulting organisms. But in Euglypha and allied forms the existence of a shell introduces a distinguishing mark by which it is possible to discriminate between the products of fission; so that the offspring can be differentiated from the parent. The parent organism, before division, builds the parts of the shell for the daughter form. These parts are arranged on the surface of that part of the protoplasm, external to the old shell, which will be subsequently separated as the daughter-cell. On this part the spicules are arranged and unite to form the new shell. The division of the nucleus takes place after that of the protoplasm, so that the daughter-cell is for some time without a nucleus. Although we can in this species recognise the daughter-cell for some time after separation from the parent by the greater transparency of its younger shell, it is nevertheless impossible to admit that the characteristics of the two animals are in any way different, for just before the separation of the two individuals a circulation of the protoplasm through both shells takes place after the manner described in the text, and there is therefore a complete intermingling of the substance of the two bodies.

The difference between the products is even greater after transverse fission of the Infusoria, for a new anus must be formed at the anterior part and a new mouth posteriorly. It is not known whether any circulation of the protoplasm takes place, as in Euglypha. But even if this does not occur, there is no reason for believing that the two products of division possess a different duration of life.

The process of fission in the Diatomaceae seems to me to be theoretically important, because here, as in the previously-mentioned Monothalamia (Euglypha, etc.), the new silicious skeleton is built up within the primary organism, but not, as in Euglypha, for the new individual only, but for both parent and daughter-cell alike³¹. If we compare the diatom shell to a box, then the two halves of the old shell would form two lids, one for each of the products of fission, while a new box is built up afresh for each of them. In this case there is an absolute equality between the products of fission, so far as the shell is concerned.

Note 11. Regeneration

A number of experiments have been recently undertaken, in connection with a prize thesis at Würzburg, in order to test the powers of regeneration possessed by various animals. In all essential respects the results confirm the statements of the older observers, such as Spallanzani. Carrière has also proved that snails can regenerate not only their horns and eyes, but also part of the head when it has been cut off, although he has shown that Spallanzani's old statement that they can regenerate the whole head, including the nervous system, is erroneous³².

Note 12. The Duration of Life in Plants

The title of the work on this subject mentioned in the Text is ‘Die Lebensdauer und Vegetationsweise der Pflanzen, ihre Ursache und ihre Entwicklung,’ F. Hildebrand, Engler’s botanische Jahrbücher, Bd. II. 1. und 2. Heft, Leipzig, 1881.

Note 13

[Many interesting facts and conclusions upon the subject of this essay will be found in a volume by Professor E. Ray Lankester, ‘On comparative Longevity in Man and the lower Animals,’ Macmillan and Co., 1870.—E. B. P.]

II.
ON HEREDITY.
1883

ON HEREDITY.
PREFACE

The following essay was my inaugural lecture as Pro-Rector of the University of Freiburg, and was delivered publicly in the hall of the University, on June 21, 1883; it first appeared in print in the following August. Only a few copies of the first edition were available for the public, and it is therefore now reprinted as a second edition, which only differs from the first in a few not unimportant improvements and additions.

The title which I have chosen requires some explanation. I do not propose to treat of the whole problem of heredity, but only of a certain aspect of it—the transmission of acquired characters which has been hitherto assumed to occur. In taking this course I may say that it was impossible to avoid going back to the foundation of all the phenomena of heredity, and to determine the substance with which they must be connected. In my opinion this can only be the substance of the germ-cells; and this substance transfers its hereditary tendencies from generation to generation, at first unchanged, and always uninfluenced in any corresponding manner, by that which happens during the life of the individual which bears it. If these views, which are indicated rather than elaborated in this paper, be correct, all our ideas upon the transformation of species require thorough modification, for the whole principle of evolution by means of exercise (use and disuse), as proposed by Lamarck, and accepted in some cases by Darwin, entirely collapses.

The nature of the present paper—which is a lecture and not an elaborate treatise—necessitates that only suggestions and not an exhaustive treatment of the subject could be given. I have also abstained from giving further details in the form of an appendix, chiefly because I could hardly have attempted to complete a treatment of the whole range of the subject, and I hope to refer again to these questions in the future, when new experiments and observations have been made.

I am very glad to see that such an important authority as Pflüger³³ has in the meantime come to the same opinion, from an entirely different direction—an opinion which forms the foundation of the views here brought forward, namely, that heredity depends upon the continuity of the molecular substance of the germ from generation to generation.

A. W.

II.
ON HEREDITY

With your permission I wish to bring before you to-day my views on a problem of general biological interest—the problem of heredity.

Heredity is the process which renders possible that persistence of organic beings throughout successive generations, which is generally thought to be so well understood and to need no special explanation. Nevertheless our minds cannot fail to be much perplexed by the multiplicity of its manifestations, and to be greatly puzzled as to its real nature. A celebrated German physiologist says³⁴, ‘Although many hands have at all times endeavoured to break the seal which hides the theory of heredity from our view, the results achieved have been but small; and we are in a certain degree justified in looking with little hope upon new efforts undertaken in this direction. We must nevertheless endeavour from time to time to ascertain how far we have advanced towards a complete explanation.’

Such a course is in every way advisable, for we are not dealing with phenomena which from their very nature are incomprehensible by man. The great complexity of the subject has alone rendered it hitherto insuperable, but in the province of heredity we certainly have not reached the limits of attainable knowledge.

From this point of view heredity bears some resemblance to certain anatomical and physiological problems, e. g. the structure and function of the human brain. Its structure—with so many millions of nerve-fibres and nerve-cells—is of such extraordinary complexity that we might well despair of ever completely understanding it. Each fibre is nevertheless distinct in itself, while its connection with the nearest nerve-cell can be frequently traced, and the function of many groups of cell elements is already known. But it would seem to be impossible to unravel the excessively complex network into which the cells and fibres are knit together; and hence to arrive at the function of each single element appears to be also beyond our reach. We have not however commenced to untie this Gordian knot without some hope of success, for who can say how far human perseverance may be able to penetrate into the mechanism of the brain, and to reveal a connected structure and a common principle in its countless elements? But surely this work will be most materially assisted by the simultaneous investigation of the structure and function of the nervous system in the lower forms of life—in the polypes and jelly-fish, worms and Crustacea. In the same way we should not abandon the hope of arriving at a satisfactory knowledge of the processes of heredity, if we consider the simplest processes of the lower animals as well as the more complex processes met with in the higher forms.

The word heredity in its common acceptation, means that property of an organism by which its peculiar nature is transmitted to its descendants. From an eagle’s egg an eagle of the same species developes; and not only are the characteristics of the species transmitted to the following generation, but even the individual peculiarities. The offspring resemble their parents among animals as well as among men.

On what does this common property of all organisms depend?

Häckel was probably the first to describe reproduction as ‘an overgrowth of the individual,’ and he attempted to explain heredity as a simple continuity of growth. This definition might be considered as a play upon words, but it is more than this; and such an interpretation rightly applied, points to the only path which, in my opinion, can lead to the comprehension of heredity.

Unicellular organisms, such as Rhizopoda and Infusoria, increase by means of fission. Each individual grows to a certain size, and then divides into two parts, which are exactly alike in size and structure, so that it is impossible to decide whether one of them is younger or older than the other. Hence in a certain sense these organisms possess immortality: they can, it is true, be destroyed, but, if protected from a violent death, they would live on indefinitely, and would only from time to time reduce the size of their overgrown bodies by division. Each individual of any such unicellular species living on the earth to-day is far older than mankind, and is almost as old as life itself.

From these unicellular organisms we can to a certain extent understand why the offspring, being in fact a part of its parents, must therefore resemble the latter. The question as to why the part should resemble the whole leads us to a new problem, that of assimilation, which also awaits solution. It is, at any rate, an undoubted fact that the organism possesses the power of taking up certain foreign substances, viz. food, and of converting them into the substance of its own body.

Among these unicellular organisms, heredity depends upon the continuity of the individual during the continual increase of its body by means of assimilation.

But how is it with the multicellular organisms which do not reproduce by means of simple division, and in which the whole body of the parent does not pass over into the offspring?

In such animals sexual reproduction is the chief means of multiplication. In no case has it always been completely wanting, and in the majority of cases it is the only kind of reproduction.

In these animals the power of reproduction is connected with certain cells which, as germ-cells, may be contrasted with those which form the rest of the body; for the former have a totally different rôle to play; they are without significance for the life of the individual³⁵, and yet they alone possess the power of preserving the species. Each of them can, under certain conditions, develope into a complete organism of the same species as the parent, with every individual peculiarity of the latter reproduced more or less completely. How can such hereditary transmission of the characters of the parent take place? how can a single reproductive cell reproduce the whole body in all its details?

Such a question could be easily answered if we were only concerned with the continuity of the substance of the reproductive cells from one generation to another; for this can be demonstrated in some cases, and is very probable in all. In certain insects the development of the egg into the embryo, that is the segmentation of the egg, begins with the separation of a few small cells from the main body of the egg. These are the reproductive cells, and at a later period they are taken into the interior of the animal and form its reproductive organs. Again, in certain small freshwater Crustacea (Daphnidae) the future reproductive cells become distinct at a very early period, although not quite at the beginning of segmentation, i. e. when the egg has divided into not more than thirty segments. Here also the cells which are separated early form the reproductive organs of the animal. The separation of the reproductive cells from those of the body takes place at a still later period, viz. at the close of segmentation, in Sagitta—a pelagic free-swimming form. In Vertebrata they do not become distinct from the other cells of the body until the embryo is completely formed. Thus, as their development shows, a marked antithesis exists between the substance of the undying reproductive cells and that of the perishable body-cells. We cannot explain this fact except by the supposition that each reproductive cell potentially contains two kinds of substance, which at a variable time after the commencement of embryonic development, separate from one another, and finally produce two sharply contrasted groups of cells.

It is evidently unimportant, as regards the question of heredity, whether this separation takes place early or late, inasmuch as the molecular constitution of the reproductive substance is determined before the beginning of development. In order to understand the growth and multiplication of cells, it must be conceded that all protoplasmic molecules possess the power of growing, that is of assimilating food, and of increasing by means of division. In the same manner the molecules of the reproductive protoplasm, when well nourished, grow and increase without altering their peculiar nature, and without modifying the hereditary tendencies derived from the parents. It is therefore quite conceivable that the reproductive cells might separate from the somatic cells much later than in the examples mentioned above, without changing the hereditary tendencies of which they are the bearers. There may be in fact cases in which such separation does not take place until after the animal is completely formed, and others, as I believe that I have shown³⁶, in which it first arises one or more generations later, viz. in the buds produced by the parent. Here also there is no ground for the belief that the hereditary tendencies of the reproductive molecules are in any way changed by the length of time which elapses before their separation from the somatic molecules. And this theoretical deduction is confirmed by observation, for from the egg of a Medusa, produced by the budding of a Polype, a Polype, in the first instance, and not a Medusa arises. Here the molecules of the reproductive substance first formed part of the Polype, and later, part of the Medusa bud, and, although they separated from the somatic cells in the bud, they nevertheless always retain the tendency to develope into a Polype.

We thus find that the reproduction of multicellular organisms is essentially similar to the corresponding process in unicellular forms; for it consists in the continual division of the reproductive cell; the only difference being that in the former case the reproductive cell does not form the whole individual, for the latter is composed of the millions of somatic cells by which the reproductive cell is surrounded. The question, ‘How can a single reproductive cell contain the germ of a complete and highly complex individual?’ must therefore be re-stated more precisely in the following form, ‘How can the substance of the reproductive cells potentially contain the somatic substance with all its characteristic properties?’

The problem which this question suggests, becomes clearer when we employ it for the explanation of a definite instance, such as the origin of multicellular from unicellular animals. There can be no doubt that the former have originated from the latter, and that the physiological principle upon which such an origin depended, is the principle of division of labour. In the course of the phyletic development of the organized world, it must have happened that certain unicellular individuals did not separate from one another immediately after division, but lived together, at first as equivalent elements, each of which retained all the animal functions, including that of reproduction. The Magosphaera planula of Häckel proves that such perfectly homogeneous cell-colonies exist³⁷, even at the present day. Division of labour would produce a differentiation of the single cells in such a colony: thus certain cells would be set apart for obtaining food and for locomotion, while certain other cells would be exclusively reproductive. In this way colonies consisting of somatic and of reproductive cells must have arisen, and among these for the first time death appeared. For in each case the somatic cells must have perished after a certain time, while the reproductive cells alone retained the immortality inherited from the Protozoa. We must now ask how it becomes possible that one kind of cell in such a colony, can produce the other kind by division? Before the differentiation of the colony each cell always produced others similar to itself. How can the cells, after the nature of one part of the colony is changed, have undergone such changes in their nature that they can now produce more than one kind of cell?

Two theories can be brought forward to solve this problem. We may turn to the old and long since abandoned nisus formativus, or adapting the name to modern times, to a phyletic force of development which causes the organism to change from time to time. This vis a tergo or teleological force compels the organism to undergo new transformations without any reference to the external conditions of life. This theory throws no light upon the numerous adaptations which are met with in every organism; and it possesses no value as a scientific explanation.

Another supposition is that the primary reproductive cells are influenced by the secondary cells of the colony, which, by their adaptability to the external conditions of life, have become somatic cells: that the latter give off minute particles which entering into the former, cause such changes in their nature that at the next succeeding cell-division they are compelled to break up into dissimilar parts.

At first sight this hypothesis seems to be quite reasonable. It is not only conceivable that particles might proceed from the somatic to the reproductive cells, but the very nutrition of the latter at the expense of the former is a demonstration that such a passage actually takes place. But a closer examination reveals immense difficulties. In the first place, the molecules of the body devoured are never simply added to those of the feeding individual without undergoing any change, but as far as we know, they are really assimilated³⁸, that is, converted into the molecules of the latter. We cannot therefore gain much by assuming that a number of molecules can pass from the growing somatic cells into the growing reproductive cells, and can be deposited unchanged in the latter, so that, at their next division, the molecules are separated to become the somatic cells of the following generation. How can such a process be conceivable, when the colony becomes more complex, when the number of somatic cells becomes so large that they surround the reproductive cells with many layers, and when at the same time by an increasing division of labour a great number of different tissues and cells are produced, all of which must originate de novo from a single reproductive cell? Each of these various elements must, ex hypothesi, give up certain molecules to the reproductive cells; hence those which are in immediate contact with the latter would obviously possess an advantage over those which are more remote. If then any somatic cell must send the same number of molecules to each reproductive cell³⁹, we are compelled to suspend all known physical and physiological conceptions, and must make the entirely gratuitous assumption of an affinity on the part of the molecules for the reproductive cells. Even if we admit the existence of this affinity, its origin and means of control remain perfectly unintelligible if we suppose that it has arisen from differentiation of the complete colony. An unknown controlling force must be added to this mysterious arrangement, in order to marshal the molecules which enter the reproductive cell in such a manner that their arrangement corresponds with the order in which they must emerge as cells at a later period. In short, we become lost in unfounded hypotheses.