Essays Upon Heredity and Kindred Biological Problems. Weismann August

and Anodonta become sexually mature in the third to the fifth year.’

      As far as I am aware but few statements exist upon the length of life in marine mollusca, and these are for the most part very inexact. The giant bivalve Tridacna gigas must attain an age of 60 to 100 years23. All Cephalopods live for at least over a year, and most of them well over ten years; and the giant forms, sometimes mistaken for ‘sea-serpents,’ must require many decades in which to attain such a remarkable size. L. Agassiz has determined the length of life in a large sea snail, Natica heros, by sorting a great number of individuals according to their sizes: he places it at 30 years24.

      I am glad to be able to communicate an observation made at the Zoological Station at Naples upon the length of life in Ascidians. The beautiful white Cionea intestinalis has settled in great numbers in an aquarium at the Station, and Professor Dohrn tells me that it produces three generations annually, and that each individual lives for about five months, and then reproduces itself and dies. External conditions accounting for this early death have not been discovered.

      It is known that the freshwater Polyzoa are annual, but it is not known whether the first individuals produced from a colony in the spring, live for the whole summer. The length of life is also unknown in single individuals of any marine Polyzoon.

      Clessin’s accurate statements upon the freshwater Mollusca, previously quoted, show that a surprisingly short length of life is the general rule. Only those forms of which the large size requires that many years shall elapse before the attainment of sexual maturity, live ten years or over (Unio, Anodonta); indeed, our largest native snail (Helix pomatia) only lives for four years, and many small species only one year, or two years if the former time is insufficient to render them sexually mature. These facts seem to indicate, as I think, that these molluscs are exposed to great destruction in the adult state, indeed to a greater extent than when they are young, or, at any rate, to an equal extent. The facts appear to be the reverse of those found among birds. The fertility is enormous; a single mussel contains several hundred thousand eggs; the destruction of young as compared with the number of eggs produced is distinctly smaller than in birds, therefore a much shorter duration of the life of each mature individual is rendered possible, and further becomes advantageous because the mature individuals are exposed to severe destruction.

      However it can only be vaguely suggested that this is the case, for positive proofs are entirely absent. Perhaps the destruction of single mature individuals does not play so important a part as the destruction of their generative organs. The ravages of parasitic animals (Trematodes) in the internal organs of snails and bivalves are well known to zoologists. The ovaries of the latter are often entirely filled with parasites, and such animals are then incapable of reproduction.

      Besides, molluscs have many enemies, which destroy them both on land and in water. In the water,—fish, frogs, newts, ducks and other water-fowl, and on land many birds, the hedgehog, toads, etc., largely depend upon them for food.

      If the principles developed in this essay apply to the freshwater Mollusca, we must then infer that snails which maintain the mature condition—the capability of reproduction—for one year, are in this state more exposed to destruction from the attacks of enemies than those species which remain sexually mature for two or three years, or that the latter suffer from a greater proportional loss of eggs and young.

Note 6. Unequal Length of Life in the two Sexes

      This inequality is frequently found among insects. The males of the remarkable little parasites infesting bees, the Strepsiptera, only live for two to three hours in the mature condition, while the wingless, maggot-like, female lives eight days: in this case, therefore, the female lives sixty-four times as long as the male. The explanation of these relations is obvious; a long life for the male would be useless to the species, while the relatively long life of the female is a necessity for the species, inasmuch as she is viviparous, and must nourish her young until their birth.

      Again, the male of Phylloxera vastatrix lives for a much shorter period than the female, and is devoid of proboscis and stomach, and takes no food: it fertilizes the female as soon as the last skin has been shed and then dies.

      Insects are not the only animals among which we find inequality in the length of life of the two sexes. Very little attention has been hitherto directed to this matter, and we therefore possess little or no accurate information as to the duration of life in the sexes, but in some cases we can draw inferences either from anatomical structure or from the mode of development. Thus, male Rotifers never possess mouth, stomach, or intestine, they cannot take food, and without doubt live much shorter lives than the females, which are provided with a complete alimentary canal. Again, the dwarf males of many parasitic Copepods—low Crustacea—and the ‘complementary males’ of Cirrhipedes (or barnacles) are devoid of stomach, and must live for a much shorter time than the females; and the male Entoniscidae (a family of which the species are endo-parasitic in the larger Crustacea), although they can feed, die after fertilizing the females; while the latter then take to a parasitic life, produce eggs, and continue to live for some time. It is supposed that the dwarf male of Bonellia viridis does not live so long by several years as the hundred times larger female, and it too has no mouth to its alimentary canal. These examples might be further increased by reference to zoological literature.

      In most cases the female lives longer than the male, and this needs no special explanation; but the converse relation is conceivable, when, for instance, the females are much rarer than the males, and the latter lose much time in seeking them. The above-mentioned case of Aglia tau probably belongs to this category.

      We cannot always decide conclusively whether the life of one sex has been lengthened or that of the other shortened; both these changes must have taken place in different cases. There is no doubt that a lengthening of life in the female has arisen in the bees and ants, for both sexes of the saw-flies, which are believed to be the ancestors of bees, only live for a few weeks. But among the Strepsiptera the shorter life of the male must have been secondarily acquired, since we only rarely meet with such an extreme case in insects.

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

23

Bronn, ‘Klassen und Ordnungen des Thierreichs,’ Bd. III. p. 466; Leipzig.

24

Bronn, l. c.

25

Cf. the article ‘Mort’ in the ‘Encyclop. Scienc. Méd.’ vol. M. p. 520.