The Different Forms of Flowers on Plants of the Same Species by Charles Robert Darwin (top fiction books of all time txt) 📖

size of the anthers was not particularly attended to in the two forms of the other heterostyled plants, but I believe that they are generally equal, as is certainly the case with those of the common primrose and cowslip.
The pistil differs in length in the two forms of every heterostyled plant, and although a similar difference is very general with the stamens, yet in the two forms of Linum grandiflorum and of Cordia they are equal. There can hardly be a doubt that the relative length of these organs is an adaptation for the safe transportal by insects of the pollen from the one form to the other. The exceptional cases in which these organs do not stand exactly on a level in the two forms may probably be explained by the manner in which the flowers are visited. With most of the species, if there is any difference in the size of the stigma of the two forms, that of the long-styled, whatever its shape may be, is larger than that of the short-styled. But here again there are some exceptions to the rule, for in the short-styled form of Leucosmia Burnettiana the stigmas are longer and much narrower than those of the long-styled; the ratio between the lengths of the stigmas in the two forms being 100 to 60. In the three Rubiaceous genera, Faramea, Houstonia and Oldenlandia, the stigmas of the short- styled form are likewise somewhat longer and narrower; and in the three forms of Oxalis sensitiva the difference is strongly marked, for if the length of the two stigmas of the long-styled pistil be taken as 100, it will be represented in the mid- and short-styled forms by the numbers 141 and 164. As in all these cases the stigmas of the short-styled pistil are seated low down within a more or less tubular corolla, it is probable that they are better fitted by being long and narrow for brushing the pollen off the inserted proboscis of an insect.
With many heterostyled plants the stigma differs in roughness in the two forms, and when this is the case there is no known exception to the rule that the papillae on the stigma of the long-styled form are longer and often thicker than those on that of the short-styled. For instance, the papillae on the long-styled stigma of Hottonia palustris are more than twice the length of those in the other form. This holds good even in the case of Houstonia coerulea, in which the stigmas are much shorter and stouter in the long-styled than in the short-styled form, for the papillae on the former compared with those on the latter are as 100 to 58 in length. The length of the pistil in the long-styled form of Linum grandiflorum varies much, and the stigmatic papillae vary in a corresponding manner. From this fact I inferred at first that in all cases the difference in length between the stigmatic papillae in the two forms was one merely of correlated growth; but this can hardly be the true or general explanation, as the shorter stigmas of the long-styled form of Houstonia have the longer papillae. It is a more probable view that the papillae, which render the stigma of the long-styled form of various species rough, serve to entangle effectually the large-sized pollen-grains brought by insects from the short-styled form, thus ensuring its legitimate fertilisation. This view is supported by the fact that the pollen-grains from the two forms of eight species in Table 6.34 hardly differ in diameter, and the papillae on their stigmas do not differ in length.
The species which are at present positively or almost positively known to be heterostyled belong, as shown in Table 6.35, to 38 genera, widely distributed throughout the world. These genera are included in fourteen Families, most of which are very distinct from one another, for they belong to nine of the several great Series, into which phanerogamic plants have been divided by Bentham and Hooker.
TABLE 6.35. List of genera including heterostyled species.
DICOTYLEDONS.
HYPERICINEAE: Cratoxylon.
ERYTHROXYLEAE: Erythroxylum. Sethia.
GERANIACEAE: Linum. Oxalis.
LYTHRACEAE: Lythrum. Neseae.
RUBIACEAE: Cinchona. Bouvardia. Manettia. Hedyotis. Oldenlandia. Houstonia. Coccocypselum. Lipostoma. Knoxia. Faramea. Psychotria. Rudgea. Suteria. Mitchella. Diodia. Borreria. Spermacoce.
PRIMULACEAE: Primula. Hottonia. Androsace.
OLEACEAE: Forsythia.
GENTIANACEAE: Menyanthes. Limnanthemum. Villarsia.
POLEMONIACEAE: Gilia.
CORDIEAE: Cordia.
BORAGINEAE: Pulmonaria.
VERBENACEAE: Aegiphila.
POLYGONEAE: Polygonum.
THYMELEAE: Thymelea.
MONOCOTYLEDONS.
PONTEDERIACEAE: Pontederia.
In some of these families the heterostyled condition must have been acquired at a very remote period. Thus the three closely allied genera, Menyanthes, Limnanthemum, and Villarsia, inhabit respectively Europe, India, and South America. Heterostyled species of Hedyotis are found in the temperate regions of North and the tropical regions of South America. Trimorphic species of Oxalis live on both sides of the Cordillera in South America and at the Cape of Good Hope. In these and some other cases it is not probable that each species acquired its heterostyled structure independently of its close allies. If they did not do so, the three closely connected genera of the Menyantheae and the several trimorphic species of Oxalis must have inherited their structure from a common progenitor. But an immense lapse of time will have been necessary in all such cases for the modified descendants of a common progenitor to have spread from a single centre to such widely remote and separated areas. The family of the Rubiaceae contains not far short of as many heterostyled genera as all the other thirteen families together; and hereafter no doubt other Rubiaceous genera will be found to be heterostyled, although a large majority are homostyled. Several closely allied genera in this family probably owe their heterostyled structure to descent in common; but as the genera thus characterised are distributed in no less than eight of the tribes into which this family has been divided by Bentham and Hooker, it is almost certain that several of them must have become heterostyled independently of one another. What there is in the constitution or structure of the members of this family which favours their becoming heterostyled, I cannot conjecture. Some families of considerable size, such as the Boragineae and Verbenaceae, include, as far as is at present known, only a single heterostyled genus. Polygonum also is the sole heterostyled genus in its family; and though it is a very large genus, no other species except P. fagopyrum is thus characterised. We may suspect that it has become heterostyled within a comparatively recent period, as it seems to be less strongly so in function than the species in any other genus, for both forms are capable of yielding a considerable number of spontaneously self-fertilised seeds. Polygonum in possessing only a single heterostyled species is an extreme case; but every other genus of considerable size which includes some such species likewise contains homostyled species. Lythrum includes trimorphic, dimorphic, and homostyled species.
Trees, bushes, and herbaceous plants, both large and small, bearing single flowers or flowers in dense spikes or heads, have been rendered heterostyled. So have plants which inhabit alpine and lowland sites, dry land, marshes and water. (6/3. Out of the 38 genera known to include heterostyled species, about eight, or 21 per cent, are more or less aquatic in their habits. I was at first struck with this fact, for I was not then aware how large a proportion of ordinary plants inhabit such stations. Heterostyled plants may be said in one sense to have their sexes separated, as the forms must mutually fertilise one another. Therefore it seemed worth while to ascertain what proportion of the genera in the Linnean classes, Monoecia, Dioecia and Polygamia, contained species which live "in water, marshes, bogs or watery places." In Sir W.J. Hooker's 'British Flora' 4th edition 1838, these three Linnean classes include 40 genera, 17 of which (i.e. 43 per cent) contain species inhabiting the just-specified stations. So that 43 per cent of those British plants which have their sexes separated are more or less aquatic in their habits, whereas only 21 per cent of heterostyled plants have such habits. I may add that the hermaphrodite classes, from Monandria to Gynandria inclusive, contain 447 genera, of which 113 are aquatic in the above sense, or only 25 per cent. It thus appears, as far as can be judged from such imperfect data, that there is some connection between the separation of the sexes in plants and the watery nature of the sites which they inhabit; but that this does not hold good with heterostyled species.)
When I first began to experimentise on heterostyled plants it was under the impression that they were tending to become dioecious; but I was soon forced to relinquish this notion, as the long-styled plants of Primula which, from possessing a longer pistil, larger stigma, shorter stamens with smaller pollen- grains, seemed to be the more feminine of the two forms, yielded fewer seeds than the short-styled plants which appeared to be in the above respects the more masculine of the two. Moreover, trimorphic plants evidently come under the same category with dimorphic, and the former cannot be looked at as tending to become dioecious. With Lythrum salicaria, however, we have the curious and unique case of the mid-styled form being more feminine or less masculine in nature than the other two forms. This is shown by the large number of seeds which it yields in whatever manner it may be fertilised, and by its pollen (the grains of which are of smaller size than those from the corresponding stamens in the other two forms) when applied to the stigma of any form producing fewer seeds than the normal number. If we suppose the process of deterioration of the male organs in the mid-styled form to continue, the final result would be the production of a female plant; and Lythrum salicaria would then consist of two heterostyled hermaphrodites and a female. No such case is known to exist, but it is a possible one, as hermaphrodite and female forms of the same species are by no means rare. Although there is no reason to believe that heterostyled plants are regularly becoming dioecious, yet they offer singular facilities, as will hereafter be shown, for such conversion; and this appears occasionally to have been effected.
We may feel sure that plants have been rendered heterostyled to ensure cross- fertilisation, for we now know that a cross between the distinct individuals of the same species is highly important for the vigour and fertility of the offspring. The same end is gained by dichogamy or the maturation of the reproductive elements of the same flower at different periods,--by dioeciousness--self-sterility--the prepotency of pollen from another individual over a plant's own pollen,--and lastly, by the structure of the flower in relation to the visits of insects. The wonderful diversity of the means for gaining the same end in this case, and in many others, depends on the nature of all the previous changes through which the species has passed, and on the more or less complete inheritance of the successive adaptations of each part to the surrounding conditions. Plants which are already well adapted by the structure of their flowers for cross-fertilisation by the aid of insects often possess an irregular corolla, which has been modelled in relation to their visits; and it would have been of little or no use to such plants to have become heterostyled. We can thus understand why it is that not a single species is heterostyled in such great families as the Leguminosae, Labiatae, Scrophulariaceae, Orchideae, etc., all of which have irregular flowers. Every known heterostyled plant, however, depends on insects for its fertilisation, and not on the wind; so that it is a rather surprising fact that only one genus, Pontederia, has a plainly irregular corolla.
Why some species are adapted for cross-fertilisation, whilst others within the same genus are not so, or if they once were, have since lost such adaptation and in consequence are now usually self-fertilised, I