Part 39

But whether the process always takes place in the form of polar bodies, and not perhaps principally, or at any rate frequently, in the form of equal cell-division, is another question. It is true that polar bodies occur in numerous plants, as we chiefly know from Strasburger’s researches[270]. Strasburger shows that cells are separated by division from the germ-cells, and perish. But it seems to me doubtful whether we must always regard their formation as the removal of half the number of ancestral germ-plasms rather than the histogenetic nucleoplasm of the germ-cell. It appears to me that histogenetic nucleoplasm must be present in the highly differentiated vegetable germ-cells, especially in the male cells, and also that it must be removed during the maturation of the cell, if my idea of the histogenetic nucleoplasm be accepted. It is very possible, as I have already mentioned, that there may be quite indifferent germ-cells, viz. cells which are entirely without specific histological structure, and in such cases histogenetic nucleoplasm would be absent; and during the maturation of such germ-cells no polar body would be formed for its removal. This view accords with the fact that polar bodies are absent in many plants. Furthermore, I am far from maintaining that in the cases where polar bodies occur, they must have the above-mentioned significance. I only wish to point out that the reduction assumed to be necessary for the nucleus of the vegetable germ-cells is not necessarily to be sought for at the close of their maturation, but perhaps even more frequently in an equal division of the germ-cells during some period of their development.

It also seems to me to be not impossible that a number of these vegetative ‘polar bodies’ may have an entirely different significance, viz. to perform some special function accessory to fertilization, as in the so-called ‘ventral canal-cells’ of the higher cryptogams and conifers. As we know that even the two polar bodies of the animal egg are not identical—although externally they are extremely similar, and although they arise in a precisely similar manner—I am even more inclined than before to consider that the very various ‘polar bodies’ of plants possess very different meanings.

But I do not feel justified in criticizing in detail the results of botanical investigation. I must leave the decision of such questions to botanists, and I only desire to state distinctly that a ‘reducing division’ of the nuclei of germ-cells must occur in plants as well as in animals.

V. CONCLUSIONS WITH REGARD TO HEREDITY.

The ideas developed in the preceding paragraphs lead to remarkable conclusions with regard to the theory of heredity,—conclusions which do not harmonize with the ideas on this subject which have been hitherto received. For if every egg expels half the number of its ancestral germ-plasms during maturation, the germ-cells of the same mother cannot contain the same hereditary tendencies, unless of course we make the supposition that corresponding ancestral germ-plasms are retained by all eggs—a supposition which cannot be sustained. For when we consider how numerous are the ancestral germ-plasms which must be contained in each nucleus, and further how improbable it is that they are arranged in precisely the same manner in all germ-cells, and finally how incredible it is that the nuclear thread should always be divided in exactly the same place to form corresponding loops or rods,—we are driven to the conclusion that it is quite impossible for the ‘reducing division’ of the nucleus to take place in an identical manner in all the germ-cells of a single ovary, so that the same ancestral germ-plasms would always be removed in the polar bodies. But if one group of ancestral germ-plasms is expelled from one egg, and a different group from another egg, it follows that no two eggs can be exactly alike as regards their contained hereditary tendencies: they must all differ. In many cases the differences will only be slight, that is, when the eggs contain very similar combinations of ancestral germ-plasms. Under other circumstances the differences will be very great, viz. when the combinations of ancestral germ-plasms retained in the egg are very different. I might here mention various other considerations; but this would lead me too far from my subject, into new theories of heredity. I hope to be able at some later period to develope further the theoretical ideas which are merely indicated in the present essay. I only wish to show that the consequences which follow from my theory upon the second division of the egg-nucleus, and the formation of the second polar body, are by no means opposed to the facts of heredity, and even explain them better than has hitherto been possible.

The fact that the children of the same parents are never entirely identical could hitherto only be rendered intelligible by the vague suggestion that the hereditary tendencies of the grandfather predominate in one, and those of the grandmother in another, while the tendencies of the great-grandfather predominate in a third, and so on. Any further explanation as to why this should happen was entirely wanting. Others even looked for an explanation to the different influences of nutrition, to which it is perfectly true that the egg is subjected in the ovary during its later development, according to its position and immediate surroundings. I had myself referred to these influences as a partial explanation[271], before I recognized clearly how extremely feeble and powerless are the influences of nourishment, as compared with hereditary tendencies. According to my theory, the differences between the children of the same parents become intelligible in a simple manner from the fact that each maternal germ-cell (I shall speak of the paternal germ-cells later on) contains a peculiar combination of ancestral germ-plasms, and thus also a peculiar combination of hereditary tendencies. These latter by their co-operation also produce a different result in each case, viz. the offspring, which are characterized by more or less pronounced individual peculiarities.

But the theory which explains individual differences by referring to the inequality of germ-cells, may be proved with a high degree of probability by an appeal to facts of an opposite kind, viz. by showing that identity between offspring only occurs when they have arisen from the same egg-cell. It is well known that occasionally some of the children of the same parents appear to be almost exactly alike, but such children are without exception twins, and there is every reason to believe that they have been derived from the _same_ egg. In other words, the two children are exactly alike because they have arisen from the same egg-cell, which could of course only contain a single combination of ancestral germ-plasms, and therefore of hereditary tendencies[272]. The factors which by their co-operation controlled the construction of the organism were the same, and consequently the results were also the same. Twins derived from a single egg are identical: this is a statement which, although not mathematically proved, may be looked upon as nearly certain. But there are also twins which do not possess this high degree of similarity, and these are even far commoner than the others. The explanation is to be found in the fact that the latter were derived from two egg-cells which were fertilized at the same time. In most cases, indeed, each twin is enclosed in its own embryonic membranes, while much less frequently both twins are enclosed in the same membranes. In one point only the proof is incomplete; for it has not yet been shown that identical twins are always derived from a single egg, since such an origin, together with a high degree of similarity, could only be established as occurring together in a small proportion of the cases. We therefore see that under conditions of nutriment which are as identical as possible, _two_ egg-cells develope into unlike twins, _one_ into identical twins; although we cannot yet affirm that the latter result invariably follows. It is conceivable that the stimulus for the production of two eggs from one may be afforded by the entrance of two spermatozoa, but these latter, as was shown above, could hardly contain identical hereditary tendencies, and thus two identical twins would not arise. It appears indeed that some cases have been observed in which differences have been exhibited by twins which were enclosed in the same embryonic membranes; but nevertheless I believe that two spermatozoa are not necessary to cause the formation of twins by a single egg. We know, it is true, from the investigations of Fol[273], that multiple impregnation produces the simultaneous beginning of several embryos in the eggs of star-fishes. But several embryos and young animals are not developed in this way, for embryonic development soon ceases, and the egg dies.

The recent observations of Born[274] upon the eggs of the frog also make it very probable that a double development is produced by the entrance of two spermatozoa into the egg, but here also only monstrosities, and not twins, were produced. On the other hand, it has been shown that in birds twins may be produced from the same egg, and there is no reason for the belief that their production is due to multiple impregnation. But if it may be assumed that human twins, when identical, have been derived from a single egg, it seems to me to be extremely probable that fertilization was also effected by a single sperm-cell. We cannot understand how such a high degree of similarity could have been produced if two sperm-cells had been made use of, for we are compelled to assume that two such cells would very rarely contain identical germ-plasms.

It is most probable that the egg-nucleus coalesces with the nucleus of a single spermatozoon, but the resulting segmentation-nucleus divides together with the cell-body itself, without the occurrence of those ontogenetic changes in the germ-plasm which normally take place. The nucleoplasm of the two daughter-cells still remains in the condition of germ-plasm, and its ontogenetic transformation begins afterwards—a transformation which must of course proceed in the same way in both cells, and must lead to the production of identical offspring. This is at least a possible explanation which we may retain until it has been either confirmed or disproved by fresh observations,—an explanation which is moreover supported by the well-known process of budding in the eggs of lower animals.

VI. RECAPITULATION.

To bring together shortly the results of this essay:—the fundamental fact upon which everything else is founded is the fact that _two_ polar bodies are expelled, as a preparation for embryonic development, from all animal eggs which require fertilization, while only _one_ such body is expelled from all parthenogenetic eggs.

This fact in the first place refutes every purely morphological explanation of the process. If it were physiologically valueless, such a phyletic reminiscence of the two successive divisions of the egg-nucleus must have been also retained by the parthenogenetic egg.

In my opinion the expulsion of the first polar body implies the removal of ovogenetic nucleoplasm when it has become superfluous after the maturation of the egg has been completed. The expulsion of the second polar body can only mean the removal of part of the germ-plasm itself, a removal by which the number of ancestral germ-plasms is reduced to one half. This reduction must also take place in the male germ-cells, although we are not able to associate it confidently with any of the histological processes of spermatogenesis which have been hitherto observed.

Parthenogenesis takes place when the whole of the ancestral germ-plasms, inherited from the parents, are retained in the nucleus of the egg-cell. Development by fertilization makes it necessary that half the number of these ancestral germ-plasms must be first expelled from the egg, the original quantity being again restored by the addition of the sperm-nucleus to the remaining half.

In both cases the beginning of embryogenesis depends upon the presence of a certain, and in both cases equal, quantity of germ-plasm. This certain quantity is produced by the addition of the sperm-nucleus to the egg requiring fertilization, and the beginning of embryogenesis immediately follows fertilization. The parthenogenetic egg contains within itself the necessary quantity of germ-plasm, and the latter enters upon active development as soon as the single polar body has removed the ovogenetic nucleoplasm. The question which I have raised on a previous occasion—‘When is the parthenogenetic egg capable of development?’—now admits of the precise answer—‘Immediately after the expulsion of the polar body.’

From the preceding facts and considerations the important conclusion results that the germ-cells of any individual do not contain the same hereditary tendencies, but are all different, in that no two of them contain exactly the same combinations of hereditary tendencies. On this fact the well-known differences between the children of the same parents depend.

But the deeper meaning of this arrangement must doubtless be sought for in the individual variability which is thus continuously kept up and is always being forced into new combinations. Thus sexual reproduction is to be explained as an arrangement which ensures an ever-varying supply of individual differences.

Footnotes for Essay VI.

Footnote 234:

See Berichten der Naturforschenden Gesellschaft zu Freiburg i. B., Band III. (1887) Heft I, ‘Ueber die Bildung der Richtungskörper bei thierischen Eiern,’ by August Weismann and C. Ischikawa.

Footnote 235:

Vol. I. p. 60.

Footnote 236:

The most recent example of this kind is afforded by the excellent work of O. Schultze, ‘Ueber die Reifung und Befruchtung des Amphibieneies,’ Zeitschr. f. wiss. Zool., Bd. XLV. 1887. Schultze has proved that two polar bodies are expelled from the egg of the Axolotl and of the frog, although all previous observers, including O. Hertwig, had been unable to find them. Thus the latter authority states as the result of an investigation specially directed towards this point, that the nucleus is transformed in a peculiar manner (‘Befruchtung des thierischen Eies,’ III. p. 81).

Footnote 237:

O. Hertwig, ‘Beiträge zur Kenntniss der Bildung, Befruchtung, und Theilung des thierischen Eies,’ Morpholog. Jahrbuch, I, II, and III. 1875-77.

Footnote 238:

H. Fol, ‘Recherches sur la fécondation et le commencement de l’hénogénie chez divers animaux.’ Genève, Bâle, Lyon, 1879.

Footnote 239:

Bütschli, ‘Entwicklungsgeschichtliche Beiträge,’ Zeitschr. f. wiss. Zool. Bd. XXIX. p. 237. 1877.

Footnote 240:

C. S. Minot, ‘Account, etc.’ Proceedings Boston Soc. Nat. Hist., vol. xix. p. 165. 1877.

Footnote 241:

F. M. Balfour, ‘Comparative Embryology.’

Footnote 242:

Nägeli, ‘Mechanisch-physiologische Theorie der Abstammungslehre,’ München und Leipzig, 1884.

Footnote 243:

See the second and fourth Essays in the present volume.

Footnote 244:

Hensen, ‘Die Grundlagen der Vererbung,’ Zeitschr. f. wiss. Landwirthschaft. Berlin, 1885, p. 749.

Footnote 245:

O. Hertwig, ‘Lehrbuch der Entwicklungsgeschichte des Menschen und der Wirbelthiere.’ Jena, 1886.

Footnote 246:

Bütschli, ‘Gedanken über die morphologische Bedeutung der sog. Richtungskörperchen,’ Biol. Centralblatt, Bd. VI. p. 5. 1884.

Footnote 247:

This observation was first published as a note at the end of the fourth Essay in the present volume. See p. 249.

Footnote 248:

Weismann, ‘Richtungskörper bei parthenogenetischen Eieren,’ Zool. Anzeiger, 1886, p. 570.

Footnote 249:

Blochmann, ‘Ueber die Richtungskörper bei den Insekteneiern,’ Biolog. Centralblatt., April 15, 1887.

Footnote 250:

F. Stuhlmann, ‘Die Reifung des Arthropodeneies nach Beobachtungen an Insekten, Spinnen, Myriapoden und Peripatus,’ Berichte der naturforschenden Gesellschaft zu Freiburg i. Br., Bd. I. p. 101.

Footnote 251:

In the summer-eggs of Rotifera I have, together with Mr. Ischikawa, observed one polar body, and we were able to establish for certain that a second is not formed. The nuclear spindle had already been observed by Tessin, and Billet had noticed polar bodies in _Philodina_, but without attaching any importance to their number. These latter observations were not conclusive proofs of the formation of polar bodies in parthenogenetic eggs, so long as it was not known whether the summer-eggs of Rotifera may develope parthenogenetically, or whether they can only develope in this way. Knowing now that parthenogenetic eggs expel only one polar body, we may perhaps be permitted to draw the conclusion that the summer-egg of a Rotifer (_Lacinularia_) which expelled only one polar body must have been a parthenogenetic egg. But I may add that we have also succeeded in directly proving the occurrence of parthenogenesis in Rotifera, as will be described in detail in another paper.

Footnote 252:

See Essay IV, Part III. p. 225.

Footnote 253:

E. Bessels, ‘Die Landois’sche Theorie, widerlegt durch das Experiment.’ Zeitschr. f. wiss. Zool. Bd. XVIII. p. 124. 1868.

Footnote 254:

l. c., p. 110.

Footnote 255:

Strasburger, ‘Neue Untersuchungen über den Befruchtungsvorgang bei den Phanerogamen als Grundlage einer Theorie der Zeugung.’ Jena, 1884.

Footnote 256:

Wilhelm Roux, ‘Ueber die Bedeutung der Kerntheilungsfiguren.’ Leipzig, 1884.

Footnote 257:

E. van Beneden, ‘Recherches sur la maturation de l’œuf, la fécondation et la division cellulaire.’ Gand et Leipzig, Paris, 1883.

Footnote 258:

J. B. Carnoy, ‘La Cytodiérèse de l’œuf, la vésicule germinative et les globules polaires de l’Ascaris megalocephala.’ Louvain, Gand, Lierre, 1886.

Footnote 259:

See p. 364.

Footnote 260:

Wilhelm Roux, ‘Beiträge zur Entwicklungsmechanik des Embryo,’ No. 3, Breslauer ärztliche Zeitschrift, 1885, p. 45.

Footnote 261:

Carnoy, ‘La Cytodiérèse chez les Arthropodes.’ Louvain, Gand, Lierre, 1885.

Footnote 262:

Flemming, ‘Neue Beiträge zur Kenntniss der Zelle.’ Arch. f. mikr. Anat. Bd. XXIX, 1887.

Footnote 263:

Carnoy, ‘La Cytodiérèse de l’œuf; la vésicule germinative et les globules polaires chez quelques Nématodes.’ Louvain, Gand, Lierre. 1886.

Footnote 264:

Hensen, ‘Die Grundlagen der Vererbung nach dem gegenwärtigen Wissenskreis,’ Zeitschr. f. wissenschaftl. Landwirthschaft, Berlin, 1885, p. 731.

Footnote 265:

See the preceding Essay on ‘The Significance of Sexual Reproduction in the theory of Natural Selection.’

Footnote 266:

E. van Beneden and Julin, ‘La Spermatogénèse chez l’Ascaride mégalocéphale.’ Brussels, 1884.

Footnote 267:

Carnoy, ‘La Cytodiérèse chez les Arthropodes.’

Footnote 268:

Gustav Platner, ‘Die Karyokinese bei den Lepidopteren als Grundlage für eine Theorie der Zelltheilung.’ Internation. Monatsschrift f. Anatomie und Histologie, Bd. III. Heft 10. Leipzig, 1886.

Footnote 269:

La Valette St. George, ‘Ueber die Genese der Samenkörper.’ Fünfte Mittheilung. Die Spermatogenese bei den Säugethieren und dem Menschen,’ Archiv f. mikrosk. Anat. Bd. XV. 1878.

Footnote 270:

Weismann, ‘Studien zur Descendenztheorie,’ ii. p. 306, Leipzig, 1876, translated by Meldola; see ‘Studies in the Theory of Descent,’ p. 680.

Footnote 271:

l. c., p. 92.

Footnote 272:

[The similar conclusion that identical ova lead to the appearance of identical individuals was drawn from the same data by Francis Galton in 1875. See ‘The history of the Twins, as a criterion of the relative powers of Nature and Nurture,’ by Francis Galton, F.R.S., Journal of the Anthropological Institute, 1875, p. 391; also by the same author, ‘Short Notes on Heredity, etc. in Twins,’ in the same Journal, 1875, p. 325.

The author investigated about eighty cases of close similarity between twins, and was able to obtain instructive details in thirty-five of these. Of the latter there were no less than seven cases ‘in which both twins suffered from some special ailment or had some exceptional peculiarity;’ in nine cases it appeared that ‘both twins are apt to sicken at the same time;’ in eleven cases there was evidence for a remarkable association of ideas; in sixteen cases the tastes and dispositions were described as closely similar. These points of identity are given in addition to the more superficial indications presented by the failure of strangers or even parents to distinguish between the twins. A very interesting part of the investigation was concerned with the after-lives of the thirty-five twins. ‘In some cases the resemblance of body and mind had continued unaltered up to old age, notwithstanding very different conditions of life,’ in the other cases ‘the parents ascribed such dissimilarity as there was, wholly, or almost wholly, to some form of illness.’

The conclusions of the author are as follows: ‘Twins who closely resembled each other in childhood and early youth, and were reared under not very dissimilar conditions, either grow unlike through the development of natural characteristics which had lain dormant at first, or else they continue their lives, keeping time like two watches, hardly to be thrown out of accord except by some physical jar. Nature is far stronger than nurture within the limited range that I have been careful to assign to the latter.’ And again, ‘where the maladies of twins are continually alike, the clocks of their two lives move regularly on, and at the same rate, governed by their internal mechanism. Necessitarians may derive new arguments from the life histories of twins.’

The above facts and conclusions held for twins of the same sex, of which at any rate the majority are shown by Kleinwächter’s observations to have been enclosed in the same embryonic membranes, and therefore presumably to have been derived from a single ovum; but in rarer cases the twins, although also invariably of the same sex, were marked by remarkable differences, greater than those which usually distinguish children of the same family. Mr. Galton met with twenty of these cases. In such twins the conditions of training, etc. had been as similar as possible, so that the evidence of the power of nature over nurture is strongly confirmed. Mr. Galton writes, ‘I have not a single case in which my correspondents speak of originally dissimilar characters having become assimilated through identity of nurture. The impression that all this evidence leaves on the mind is one of wonder whether nurture can do anything at all, beyond giving instruction and professional training.’

The fact that twins produced from a single ovum seem to be invariably of the same sex is in itself extremely interesting, for it proves that the sex of the individual is predetermined in the fertilized ovum.—E. B. P.]

Footnote 273:

Fol, Recherches sur la fécondation et le commencement de l’hénogénie: Genève, Bâle, Lyon. 1879.

Footnote 274:

Born, ‘Ueber Doppelbildungen beim Frosch und deren Entstehung.’ Breslauer ärztl. Zeitschrift, 1882.

VII.

ON THE SUPPOSED BOTANICAL PROOFS

OF THE

TRANSMISSION OF ACQUIRED CHARACTERS.

1888.

From ‘Biologisches Centralblatt,’ Bd. VIII. Nr. 3 and 4, pages 65 and 97: April 1888.

VII.

ON THE SUPPOSED BOTANICAL PROOFS OF THE TRANSMISSION OF ACQUIRED CHARACTERS.