Essays Upon Heredity and Kindred Biological Problems
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It must then be admitted that the dependence of the duration of life upon the external conditions of existence is alike common to plants and animals. In both kingdoms the high multicellular forms with well-differentiated organs contain the germs of death, while the low unicellular organisms are potentially immortal. Furthermore, an undying succession of reproductive cells is possessed by all the higher forms, although this may be but poor consolation to the conscious individual which perishes. Johannes Müller is therefore right, when in the sentence quoted at the beginning of my lecture, he speaks of an ‘appearance of immortality’ which passes from each individual into that which succeeds it. That which remains over, that which persists, is not the individual itself,—not the complex aggregate of cells which is conscious of itself,—but an individuality which is outside its consciousness, and of a low order,—an individuality which is made up of a single cell, which arises from the conscious individual. I might here conclude, but I wish first, in a few words, to protect myself against a possible misunderstanding.
I have repeatedly spoken of immortality, first of the unicellular organism, and secondly of the reproductive cell. By this word I have merely intended to imply a duration of time which appears to be endless to our human faculties. I have no wish to enter into the question of the cosmic or telluric origin of life on the earth. An answer to this question will at once decide whether the power of reproduction possessed by these cells is in reality eternal or only immensely prolonged, for that which is without beginning is, and must be, without end.
The supposition of a cosmic origin of life can only assist us if by its means we can altogether dispense with any theory of spontaneous generation. The mere shifting of the origin of life to some other far-off world cannot in any way help us. A truly cosmic origin in its widest significance will rigidly limit us to the statement—omne vivum e vivo—to the idea that life can only arise from life, and has always so arisen,—to the conclusion that organic beings are eternal like matter itself.
Experience cannot help us to decide this question; we do not know whether spontaneous generation was the commencement of life on the earth, nor have we any direct evidence for the idea that the process of development of the living world carries the end within itself, or for the converse idea that the end can only be brought about by means of some external force.
I admit that spontaneous generation, in spite of all vain efforts to demonstrate it, remains for me a logical necessity. We cannot regard organic and inorganic matter as independent of each other and both eternal, for organic matter is continually passing, without residuum, into the inorganic. If the eternal and indestructible are alone without beginning, then the non-eternal and destructible must have had a beginning. But the organic world is certainly not eternal and indestructible in that absolute sense in which we apply these terms to matter itself. We can, indeed, kill all organic beings and thus render them inorganic at will. But these changes are not the same as those which we induce in a piece of chalk by pouring sulphuric acid upon it; in this ease we only change the form, and the inorganic matter remains. But when we pour sulphuric acid upon a worm, or when we burn an oak tree, these organisms are not changed into some other animal and tree, but they disappear entirely as organized beings and are resolved into inorganic elements. But that which can be completely resolved into inorganic matter must have also arisen from it, and must owe its ultimate foundation to it. The organic might be considered eternal if we could only destroy its form, but not its nature.
It therefore follows that the organic world must once have arisen, and further that it will at some time come to an end. Hence we must speak of the eternal duration of unicellular organisms and of reproductive cells in the Metazoa and Metaphyta in that particular sense which signifies, when measured by our standards, an immensely long time.
Yet who can maintain that he has discovered the right answer to this important question? And even though the discovery were made, can any one believe that by its means the problem of life would be solved? If it were established that spontaneous generation did actually occur, a new question at once arises as to the conditions under which the occurrence became possible. How can we conceive that dead inorganic matter could have come together in such a manner as to form living protoplasm, that wonderful and complex substance which absorbs foreign material and changes it into its own substance, in other words grows and multiplies?
And so, in discussing this question of life and death, we come at last—as in all provinces of human research—upon problems which appear to us to be, at least for the present, insoluble. In fact it is the quest after perfected truth, not its possession, that falls to our lot, that gladdens us, fills up the measure of our life, nay! hallows it.
APPENDIX
Note 1. The Duration of Life among Birds
There is less exact knowledge upon this subject than we might expect, considering the existing number of ornithologists and ornithological societies with their numerous publications. It has neither been possible nor necessary for my purpose to look up all the widely-scattered references which are to be found upon the subject. Many of these are doubtless unknown to me; for we are still in want of a compilation of accurately determined observations in this department of zoology. I print the few facts which I have been able to collect, as a slight contribution towards such a compilation.
Small singing birds live from eight to eighteen years: the nightingale, in captivity, eight years, but longer according to some writers: the blackbird, in captivity, twelve years, but both these birds live longer in the natural state. A ‘half-bred nightingale built its nest for nine consecutive years in the same garden’ (Naumann, ‘Vögel Deutschlands,’ p. 76).
Canary birds in captivity attain an age of twelve to fifteen years (l. c., p. 76).
Ravens have lived for almost a hundred years in captivity (l. c., Bd. I. p. 125).
Magpies in captivity live twenty years, and, ‘without doubt,’ much longer in the natural state (l. c., p. 346).
Parrots ‘in captivity have reached upwards of a hundred years’ (l. c., p. 125).
A single instance of the cuckoo (alluded to in the text) is mentioned by Naumann as reaching the age of thirty-two years (l. c., p. 76).
Fowls live ten to twenty years, the golden pheasant fifteen years, the turkey sixteen years, and the pigeon ten years (Oken, ‘Naturgeschichte, Vögel,’ p. 387).
A golden eagle which ‘died at Vienna in the year 1719, had been captured 104 years previously’ (Brehm, ‘Leben der Vögel,’ p. 72).
A falcon (species not mentioned) is said to have attained an age of 162 years (Knauer, ‘Der Naturhistoriker,’ Vienna, 1880).
A white-headed vulture which was taken in 1706 died in the Zoological Gardens at Vienna (Schönbrunn) in 1824, thus living 118 years in captivity (l. c.).
The example of the bearded vulture, mentioned in the text, is quoted from Schinz’s ‘Vögel der Schweiz,’ p. 196.
The wild goose must live for upwards of 100 years, according to Naumann (l. c., p. 127). The proof of this is not, however, forthcoming. A wild goose which had been wounded reached its eighteenth year in captivity.
Swans are said to have lived 300 years(?), (Naumann, l. c., p. 127).
It is evident that observations upon the duration of life in wild birds can only rarely be made, and that they are usually the result of chance and cannot be verified. It is on this account all the more to be desired that every ascertained fact should be collected.
If the long life of birds has been correctly interpreted as compensation for their feeble fertility and for the great mortality of their young, it will be possible to estimate the length of life in a species, without direct observation, if we only know its fertility and the percentage of individuals destroyed. This percentage can, however, at best, be known only as an average. If we consider, for example, the enormous number of sea birds which breed in summer on the rocks and cliffs of the northern seas, and if we remember that the majority of these birds lay but one, or at most two eggs yearly, and that their young are exposed to very many destructive agencies, we are forced to the conclusion that they must possess a very long life, so that the breeding period may be many times repeated. Their number does not diminish. Year after year countless numbers of these birds cover the rocks, from summit to sea line; millions of them rest there, and rise in the air like a thick cloud whenever they are disturbed. Even in those localities which are every year visited by man in order to effect their capture, the number does not appear to decrease, unless the birds are disturbed and are therefore prompted to seek other breeding-places. From the small island of St. Kilda, off Scotland, 20,000 young gannets (Sula) and an immense number of eggs are annually collected; and although this bird only lays a single egg yearly and takes four years to attain maturity, the numbers do not diminish6. 30,000 sea-gulls’ eggs and 20,000 terns’ eggs are yearly exported from the breeding-places on the island of Sylt, but in this case it appears that a systematic disturbance of the birds is avoided by the collectors, and no decrease in their numbers has yet taken place7. The destruction of northern birds is not only caused by man, but also by various predaceous mammals and birds. Indeed the dense mass of birds which throng the cliffs is a cause of destruction to many of the young and to the eggs, which are pushed over the edge of the rocks. According to Brehm the foot of these cliffs is ‘always covered with blood and the dead bodies of fledglings.’
Such birds must attain a great age or they would have been exterminated long ago: the minimum duration of life necessary for the maintenance of the species must in their case be a very high one.
Note 2. The Duration of Life among Mammals
The statements upon this subject in the text are taken from many sources; from Giebel’s ‘Säugethiere,’ from Oken’s ‘Naturgeschichte,’ from Brehm’s ‘Illustrirtem Thierleben,’ and from an essay of Knauer in the ‘Naturhistoriker,’ Vienna, 1880.
Note 3. The Duration of Life among Mature Insects
A short statement of the best established facts which I have been able to find is given below. I have omitted the lengthening of imaginal life which is due to hybernation in certain species. In almost all orders of insects there are certain species which emerge from the pupa in the autumn, but which first reproduce in the following spring. The time spent in the torpid condition during winter cannot of course be reckoned with the active life of the species, for its vital activity is either entirely suspended for a time by freezing (Anabiosis: Preyer8), or it is at any rate never more than a vita minima, with a reduction of assimilation to its lowest point.
The following account does not make any claim to contain all or even most of the facts scattered through the enormous mass of entomological literature, and much less all that is privately known by individual entomologists. It must therefore be looked upon as merely a first attempt, a nucleus, around which the principal facts can be gradually collected. It is unnecessary to give any special information as to the duration of larval life, for numerous and exact observations upon this part of the subject are contained in all entomological works.
I. Orthoptera
Gryllotalpa. The eggs are laid in June or July, and the young are hatched in from two to three weeks; they live through the winter, and become sexually mature in the following May or June. ‘When the female has deposited her eggs, her body collapses, and afterwards she does not survive much longer than a month.’ ‘According as the females are younger or older, they live a longer or shorter life, and hence some females are even found in the autumn’ (Rösel, ‘Insektenbelustigungen,’ Bd. II. p. 92). Rösel believes that the female watches the eggs until they are hatched, and this explains the fact that she outlives the process of oviposition by about a month. It is not stated whether the males die at an earlier period.
Gryllus campestris becomes sexually mature in May, and sings from June till October, ‘when they all die’ (Oken, ‘Naturgeschichte,’ Bd. II. Abth. iii. p. 1527). It is hardly probable that any single individual lives for the whole summer; probably, as in the case of Gryllotalpa, the end of the life of those individuals which first become mature, overlaps the beginning of the life of others which reach maturity at a later date.
Locusta viridissima and L. verrucivora are mature at the end of August; they lay their eggs in the earth during the first half of September and then die. It is probable that the females do not live for more than four weeks in the mature state. It is not known whether the males of this or other species of locusts live for a shorter period.
I have found Locusta cantans in plenty, from the beginning of September to the end of the month. In captivity they die after depositing their eggs: the males are probably more short-lived, for towards the middle and end of September they are much less plentiful than the females.
Acridium migratorium ‘dies after the eggs are laid’ (Oken, ‘Naturgeschichte’).
The male Termes probably live for a short time only, although exact observations upon the point are wanting. The females ‘seem sometimes to live four or five years,’ as I gather from a letter from Dr. Hagen, of Cambridge, Mass., U.S.A.
Ephemeridae. Rösel, speaking of Ephemera vulgata (‘Insektenbelustigungen,’ Bd. II. der Wasserinsekten, 2te Klasse, p. 60 et seq.), says:—‘Their flight commences at sunset, and comes to an end before midnight, when the dew begins to fall.’ ‘The pairing generally takes place at night and lasts but a short time. As soon as the insects have shed their last skin, in the afternoon or evening, they fly about in thousands, and pair almost immediately; but by the next day they are all dead. They continue to emerge for many days, so that when yesterday’s swarm is dead, to-day a new swarm is seen emerging from the water towards the evening.’ ‘They not only drop their eggs in the water, but wherever they may happen to be,—on trees, bushes, or the earth. Birds, trout and other fish lie in wait for them.’
Dr. Hagen writes to me—‘It is only in certain species that life is so short. The female Palingenia does not live long enough to complete the last moult of the sub-imago. I believe that a female imago has never been seen. The male imago, often half in its sub-imago skin, fertilizes the female sub-imago and immediately the contents of both ovaries are extruded, and the insect dies. It is quite possible that the eggs pass out by rupturing the abdominal segments.’
Libellula. All dragon-flies live in the imago condition for some weeks; at first they are not capable of reproduction, but after a few days they pair.
Lepisma saccharina. An individual lived for two years in a pill-box, without any food except perhaps a little Lycopodium dust9.
II. Neuroptera
Phryganids ‘live in the imago stage for at least a week and probably longer, apparently without taking food’ (letter from Dr. Hagen).
According to the latest researches Phrygane grandis10 never contains food in its alimentary canal, but only air, although it contains the latter in such quantities that the anterior end of the chylific ventricle is dilated by it.
III. Strepsiptera
The larva requires for its development a rather shorter time than that which is necessary for the grub of the bee into the body of which it has bored. The pupa stage lasts eight to ten days. The male, which flies about in a most impetuous manner, lives only two to three hours, while the female lives for some days. Possibly the pairing does not take place until the female is two to three days old. The viviparous female seems to produce young only once in a lifetime, and then dies: it is at present uncertain whether she also produces young parthenogenetically (cf. Siebold, ‘Ueber Paedogenesis der Strepsipteren,’ Zeitschr. f. Wissensch. Zool., Band. XX, 1870).
IV. Hemiptera
Aphis. Bonnet (‘Observations sur les Pucerons,’ Paris, 1745) had a parthenogenetic female of Aphis euonymi in his possession for thirty-one days, from its birth, during which time it brought forth ninety-five larvae. Gleichen kept a parthenogenetic female of Aphis mali fifteen to twenty-three days.
Aphis foliorum ulmi. The mother of a colony which leaves the egg in May is 2‴ long at the end of July: it therefore lives for at least two and a half months (De Geer, ‘Abhandlungen zur Geschichte der Insekten,’ 1783, III. p. 53).
Phylloxera vastatrix. The males are merely ephemeral sexual organisms, they have no proboscis and no alimentary canal, and die immediately after fertilizing the female.
Pemphigus terebinthi. The male as well as the female sexual individuals are wingless and without a proboscis; they cannot take food and consequently live but a short time,—far shorter than the parthenogenetic females of the same species (Derbès, ‘Note sur les aphides du pistachier térébinthe,’ Ann. des sci. nat., Tom. XVII, 1872).
Cicada. In spite of the numerous and laborious descriptions of the Cicadas which have appeared during the last two centuries, I can only find precise statements as to the duration of life in the mature insect in a single species. P. Kalm, writing upon the North American Cicada septemdecim, which sometimes appears in countless numbers, states that ‘six weeks after (such a swarm had been first seen) they had all disappeared.’ Hildreth puts the life of the female at from twenty to twenty-five days. This agrees with the fact that the Cicada lays many hundred eggs (Hildreth states a thousand); sixteen to twenty at a time being inserted into a hole which is bored in wood, so that the female takes some time to lay her eggs (Oken, ‘Naturgeschichte,’ 2ter Bd. 3te Abth. p. 1588 et seq.).
Acanthia lectularia. No observations have been made upon the bed bug from which the normal length of its life can be ascertained, but many statements tend to show that it is exceedingly long-lived, and this is advantageous for a parasite of which the food (and consequently growth and reproduction) is extremely precarious. They can endure starvation for an astonishingly long period, and can survive the most intense cold. Leunis (‘Zoologie,’ p. 659) mentions the case of a female which was shut up in a box and forgotten: after six months’ starvation it was found not only alive but surrounded by a circle of lively young ones. Göze found bugs in the hangings of an old bed which had not been used for six years: ‘they appeared white like paper.’ I have myself observed a similar case, in which the starving animals were quite transparent. De Geer placed some bugs in an unheated room in the cold winter of 1772, when the thermometer fell to -33°C: they passed the whole winter in a state of torpidity, but revived in the following May. (De Geer, Bd. III. p. 165, and Oken, ‘Naturgeschichte,’ 2ter Bd. 3te Abth. p. 1613.)
V. Diptera
Pulex irritans. Oken says of the flea (‘Naturgeschichte,’ Bd. II. Abth. 2, p. 759) that ‘death follows the deposition of the eggs in the course of two or three days, even if the opportunity of sucking blood is given them.’ The length of time which intervenes between the emergence from the cocoon and fertilization or the deposition of eggs is not stated.
Sarcophaga carnaria. The female fly dies ten to twelve hours after the birth of the viviparous larvae; the time intervening between the exit from the cocoon and the birth of the young is not given (Oken, quoting Réaumur, ‘Mém. p. s. à l’hist. Insectes,’ Paris, 1740-48, IV).
Musca domestica. In the summer the common house-fly begins to lay eggs eight days after leaving the cocoon: she then lays several times. (See Gleichen, ‘Geschichte der gemeinen Stubenfliege,’ Nuremberg, 1764.)
Eristalis tenax. The larva of this large fly lives in liquid manure, and has been described and figured by Réaumur as the rat-tailed larva. I kept a female which had just emerged from the cocoon, from August 30th till October 4th, in a large gauze-covered glass vessel. The insect soon learnt to move freely about in its prison, without attempting to escape; it flew round in circles, with a characteristic buzzing sound, and obtained abundant nourishment from a solution of sugar, provided for it. From September 12th it ceased to fly about, except when frightened, when it would fly a little way off. I thought that it was about to die, but matters took an unexpected turn, and on the 26th of September it laid a large packet of eggs, and again on the 29th of the same month another packet of similar size. The flight of the animal had been probably impeded by the weight of the mass of ripe eggs in its body. The deposition of eggs was probably considerably retarded in this case, because fertilization had not taken place. The fly died on the 4th of October, having thus lived for thirty-five days. Unfortunately, I have been unable to make any experiments as to the duration of life in the female when males are also present.
VI. Lepidoptera
I am especially indebted to Mr. W. H. Edwards11, of Coalburgh, W. Virginia, and to Dr. Speyer, of Rhoden, for valuable letters relating to this order.
The latter writes, speaking of the duration of life in imagos generally:—‘It is, to my mind, improbable that any butterfly can live as an imago for a twelvemonth. Specimens which have lived through the winter are only rarely seen in August, even when the summer is late. A worn specimen of Vanessa cardui has, for instance, been found at this time’ (‘Entomolog. Nachrichten,’ 1881, p. 146).
In answer to my question as to whether the fact that certain Lepidoptera take no solid or liquid food, and are, in fact, without a functional mouth, may be considered as evidence for an adaptation of the length of life to the rapid deposition of eggs, Dr. Speyer replies:—‘The wingless females of the Psychidae do not seem to possess a mouth, at any rate I cannot find one in Psyche unicolor (graminella). They do not leave the case during life, and certainly do not drink water. The same is true of the wingless female of Heterogynis, and of Orgyia ericae, and probably of all the females of the genus Orgyia; and as far as I can judge from cabinet specimens, it is probably true of the males of Heterogynis and Psyche. I have never seen the day-flying Saturnidae, Bombycidae, and other Lepidoptera with a rudimentary proboscis, settle in damp places, or suck any moist substance, and I doubt if they would ever do this. The sucking apparatus is probably deficient.’
In answer to my question as to whether the males of any species of butterfly or moth are known to pass a life of different length from that of the female, Dr. Speyer stated that he knew of no observations on this point.
The following are the only instances of well-established direct observations upon single individuals, in my possession12:—
Pieris napi, var. bryoniae [male] and [female], captured on the wing: lived in confinement ten days, and were then killed.
Vanessa prorsa lived at most ten days in confinement.
Vanessa urticae lived ten to thirteen days in confinement.
Papilio ajax. According to a letter from Mr. W. H. Edwards, the female, when she leaves the pupa, contains unripe eggs in her body, and lives for about six weeks—calculating from the first appearance of this butterfly to the disappearance of the same generation13. The males live longer, and continue to fly when very worn and exhausted. A worn female is very seldom seen;—‘I believe the female does not live long after laying her eggs, but this takes some days, and probably two weeks.’