The Effects of Cross & Self-Fertilisation in the Vegetable Kingdom · Charles Darwin
GENERAL RESULTS.
There is another subject on which some light is thrown by the facts given in this volume, namely, hybridisation. It is notorious that when distinct species of plants are crossed, they produce with the rarest exceptions fewer seeds than the normal number. This unproductiveness varies in different species up to sterility so complete that not even an empty capsule is formed; and all experimentalists have found that it is much influenced by the conditions to which the crossed species are subjected. The pollen of each species is strongly prepotent over that of any other species, so that if a plant’s own pollen is placed on the stigma some time after foreign pollen has been applied to it, any effect from the latter is quite obliterated. It is also notorious that not only the parent species, but the hybrids raised from them are more or less sterile; and that their pollen is often in a more or less aborted condition. The degree of sterility of various hybrids does not always strictly correspond with the degree of difficulty in uniting the parent forms. When hybrids are capable of breeding inter se, their descendants are more or less sterile, and they often become still more sterile in the later generations; but then close interbreeding has hitherto been practised in all such cases. The more sterile hybrids are sometimes much dwarfed in stature, and have a feeble constitution. Other facts could be given, but these will suffice for us. Naturalists formerly attributed all these results to the difference between species being fundamentally distinct from that between the varieties of the same species; and this is still the verdict of some naturalists.
The results of my experiments in self-fertilising and cross-fertilising the individuals or the varieties of the same species, are strikingly analogous with those just given, though in a reversed manner. With the majority of species flowers fertilised with their own pollen yield fewer, sometimes much fewer seeds, than those fertilised with pollen from another individual or variety. Some self-fertilised flowers are absolutely sterile; but the degree of their sterility is largely determined by the conditions to which the parent plants have been exposed, as was well exemplified in the case of Eschscholtzia and Abutilon. The effects of pollen from the same plant are obliterated by the prepotent influence of pollen from another individual or variety, although the latter may have been placed on the stigma some hours afterwards. The offspring from self-fertilised flowers are themselves more or less sterile, sometimes highly sterile, and their pollen is sometimes in an imperfect condition; but I have not met with any case of complete sterility in self-fertilised seedlings, as is so common with hybrids. The degree of their sterility does not correspond with that of the parent-plants when first self-fertilised. The offspring of self-fertilised plants suffer in stature, weight, and constitutional vigour more frequently and in a greater degree than do the hybrid offspring of the greater number of crossed species. Decreased height is transmitted to the next generation, but I did not ascertain whether this applies to decreased fertility.
I have elsewhere shown that by uniting in various ways dimorphic or trimorphic heterostyled plants, which belong to the same undoubted species, we get another series of results exactly parallel with those from crossing distinct species. (12/18. ‘Journal of the Linnean Society Botany’ volume 10 1867 page 393.) Plants illegitimately fertilised with pollen from a distinct plant belonging to the same form, yield fewer, often much fewer seeds, than they do when legitimately fertilised with pollen from a plant belonging to a distinct form. They sometimes yield no seed, not even an empty capsule, like a species fertilised with pollen from a distinct genus. The degree of sterility is much affected by the conditions to which the plants have been subjected. (12/19. ‘Journal of the Linnean Society Botany’ volume 8 1864 page 180.) The pollen from a distinct form is strongly prepotent over that from the same form, although the former may have been placed on the stigma many hours afterwards. The offspring from a union between plants of the same form are more or less sterile, like hybrids, and have their pollen in a more or less aborted condition; and some of the seedlings are as barren and as dwarfed as the most barren hybrid. They also resemble hybrids in several other respects, which need not here be specified in detail,--such as their sterility not corresponding in degree with that of the parent plants,--the unequal sterility of the latter, when reciprocally united,--and the varying sterility of the seedlings raised from the same seed-capsule.
We thus have two grand classes of cases giving results which correspond in the most striking manner with those which follow from the crossing of so-called true and distinct species. With respect to the difference between seedlings raised from cross and self-fertilised flowers, there is good evidence that this depends altogether on whether the sexual elements of the parents have been sufficiently differentiated, by exposure to different conditions or by spontaneous variation. It is probable that nearly the same conclusion may be extended to heterostyled plants; but this is not the proper place for discussing the origin of the long-styled, short-styled and mid-styled forms, which all belong to the same species as certainly as do the two sexes of the same species. We have therefore no right to maintain that the sterility of species when first crossed and of their hybrid offspring, is determined by some cause fundamentally different from that which determines the sterility of the individuals both of ordinary and of heterostyled plants when united in various ways. Nevertheless, I am aware that it will take many years to remove this prejudice.
There is hardly anything more wonderful in nature than the sensitiveness of the sexual elements to external influences, and the delicacy of their affinities. We see this in slight changes in the conditions of life being favourable to the fertility and vigour of the parents, while certain other and not great changes cause them to be quite sterile without any apparent injury to their health. We see how sensitive the sexual elements of those plants must be, which are completely sterile with their own pollen, but are fertile with that of any other individual of the same species. Such plants become either more or less self-sterile if subjected to changed conditions, although the change may be far from great. The ovules of a heterostyled trimorphic plant are affected very differently by pollen from the three sets of stamens belonging to the same species. With ordinary plants the pollen of another variety or merely of another individual of the same variety is often strongly prepotent over its own pollen, when both are placed at the same time on the same stigma. In those great families of plants containing many thousand allied species, the stigma of each distinguishes with unerring certainty its own pollen from that of every other species.
There can be no doubt that the sterility of distinct species when first crossed, and of their hybrid offspring, depends exclusively on the nature or affinities of their sexual elements. We see this in the want of any close correspondence between the degree of sterility and the amount of external difference in the species which are crossed; and still more clearly in the wide difference in the results of crossing reciprocally the same two species;--that is, when species A is crossed with pollen from B, and then B is crossed with pollen from A. Bearing in mind what has just been said on the extreme sensitiveness and delicate affinities of the reproductive system, why should we feel any surprise at the sexual elements of those forms, which we call species, having been differentiated in such a manner that they are incapable or only feebly capable of acting on one another? We know that species have generally lived under the same conditions, and have retained their own proper characters, for a much longer period than varieties.
Long-continued domestication eliminates, as I have shown in my ‘Variation under Domestication,’ the mutual sterility which distinct species lately taken from a state of nature almost always exhibit when intercrossed; and we can thus understand the fact that the most different domestic races of animals are not mutually sterile. But whether this holds good with cultivated varieties of plants is not known, though some facts indicate that it does. The elimination of sterility through long-continued domestication may probably be attributed to the varying conditions to which our domestic animals have been subjected; and no doubt it is owing to this same cause that they withstand great and sudden changes in their conditions of life with far less loss of fertility than do natural species. From these several considerations it appears probable that the difference in the affinities of the sexual elements of distinct species, on which their mutual incapacity for breeding together depends, is caused by their having been habituated for a very long period each to its own conditions, and to the sexual elements having thus acquired firmly fixed affinities. However this may be, with the two great classes of cases before us, namely, those relating to the self-fertilisation and cross-fertilisation of the individuals of the same species, and those relating to the illegitimate and legitimate unions of heterostyled plants, it is quite unjustifiable to assume that the sterility of species when first crossed and of their hybrid offspring, indicates that they differ in some fundamental manner from the varieties or individuals of the same species.
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