The Different Forms of Flowers on Plants of the Same Species by Charles Robert Darwin (rainbow fish read aloud txt) 📕

of gradations between the cleistogamic and perfect flowers. But that the former owe their origin wholly to arrested development is by no means the case; for various parts have been specially modified, so as to aid in the self-fertilisation of the flowers, and as a protection to the pollen; for instance, the hook-shaped pistil in Viola and in some other genera, by which the stigma is brought close to the fertile anthers,- -the rudimentary corolla of Specularia modified into a perfectly closed tympanum, and the sheath of Monochoria modified into a closed sack,--the excessively thin coats of the pollen-grains,--the anthers not being all equally aborted, and other such cases. Moreover Mr. Bennett has shown that the buds of the cleistogamic and perfect flowers of Impatiens differ at a very early period of growth.
The degree to which many of the most important organs in these degraded flowers have been reduced or even wholly obliterated, is one of their most remarkable peculiarities, reminding us of many parasitic animals. In some cases only a single anther is left, and this contains but few pollen-grains of diminished size; in other cases the stigma has disappeared, leaving a simple open passage into the ovarium. It is also interesting to note the complete loss of trifling points in the structure or functions of certain parts, which though of service to the perfect flowers, are of none to the cleistogamic; for instance the collecting hairs on the pistil of Specularia, the glands on the calyx of the Malpighiaceae, the nectar-secreting appendages to the lower stamens of Viola, the secretion of nectar by other parts, the emission of a sweet odour, and apparently the elasticity of the valves in the buried capsules of Viola odorata. We here see, as throughout nature, that as soon as any part or character becomes superfluous it tends sooner or later to disappear.
Another peculiarity in these flowers is that the pollen-grains generally emit their tubes whilst still enclosed within the anthers; but this is not so remarkable a fact as was formerly thought, when the case of Asclepias was alone known. (8/28. The case of Asclepias was described by R. Brown. Baillon asserts 'Adansonia' tome 2 1862 page 58, that with many plants the tubes are emitted from pollen-grains which have not come into contact with the stigma; and that they may be seen advancing horizontally through the air towards the stigma. I have observed the emission of the tubes from the pollen-masses whilst still within the anthers, in three widely distinct Orchidean genera namely Aceras, Malaxis, and Neottia: see 'The Various Contrivances by which Orchids are Fertilised' 2nd edition page 258.) It is, however, a wonderful sight to behold the tubes directing themselves in a straight line to the stigma, when this is at some little distance from the anthers. As soon as they reach the stigma or the open passage leading into the ovarium, no doubt they penetrate it, guided by the same means, whatever these may be, as in the case of ordinary flowers. I thought that they might be guided by the avoidance of light: some pollen-grains of a willow were therefore immersed in an extremely weak solution of honey, and the vessel was placed so that the light entered only in one direction, laterally or from below or from above, but the long tubes were in each case protruded in every possible direction.
As cleistogamic flowers are completely closed they are necessarily self- fertilised, not to mention the absence of any attraction to insects; and they thus differ widely from the great majority of ordinary flowers. Delpino believes that cleistogamic flowers have been developed in order to ensure the production of seeds under climatic or other conditions which tend to prevent the fertilisation of the perfect flowers. (8/29. 'Sull' Opera la Distribuzione dei Sessi nelle Piante' 1867 page 30.) I do not doubt that this holds good to a certain limited extent, but the production of a large supply of seeds with little consumption of nutrient matter or expenditure of vital force is probably a far more efficient motive power. The whole flower is much reduced in size; but what is much more important, an extremely small quantity of pollen has to be formed, as none is lost through the action of insects or the weather; and pollen contains much nitrogen and phosphorus. Von Mohl estimated that a single cleistogamic anther-cell of Oxalis acetosella contained from one to two dozen pollen-grains; we will say 20, and if so the whole flower can have produced at most 400 grains; with Impatiens the whole number may be estimated in the same manner at 250; with Leersia at 210; and with Viola nana at only 100. These figures are wonderfully low compared with the 243,600 pollen-grains produced by a flower of Leontodon, the 4,863 by an Hibiscus, or the 3,654,000 by a Paeony. (8/30. The authorities for these statements are given in my 'Effects of Cross and Self-Fertilisation' page 376.) We thus see that cleistogamic flowers produce seeds with a wonderfully small expenditure of pollen; and they produce as a general rule quite as many seeds as the perfect flowers.
That the production of a large number of seeds is necessary or beneficial to many plants needs no evidence. So of course is their preservation before they are ready for germination; and it is one of the many remarkable peculiarities of the plants which bear cleistogamic flowers, that an incomparably larger proportion of them than of ordinary plants bury their young ovaries in the ground;--an action which it may be presumed serves to protect them from being devoured by birds or other enemies. But this advantage is accompanied by the loss of the power of wide dissemination. No less than eight of the genera in the list at the beginning of this chapter include species which act in this manner, namely, several kinds of Viola, Oxalis, Vandellia, Linaria, Commelina, and at least three genera of Leguminosae. The seeds also of Leersia, though not buried, are concealed in the most perfect manner within the sheaths of the leaves. Cleistogamic flowers possess great facilities for burying their young ovaries or capsules, owing to their small size, pointed shape, closed condition and the absence of a corolla; and we can thus understand how it is that so many of them have acquired this curious habit.
It has already been shown that in about 32 out of the 55 genera in the list just referred to, the perfect flowers are irregular; and this implies that they have been specially adapted for fertilisation by insects. Moreover three of the genera with regular flowers are adapted by other means for the same end. Flowers thus constructed are liable during certain seasons to be imperfectly fertilised, namely, when the proper insects are scarce; and it is difficult to avoid the belief that the production of cleistogamic flowers, which ensures under all circumstances a full supply of seed, has been in part determined by the perfect flowers being liable to fail in their fertilisation. But if this determining cause be a real one, it must be of subordinate importance, as four of the genera in the list are fertilised by the wind; and there seems no reason why their perfect flowers should fail to be fertilised more frequently than those in any other anemophilous genus. In contrast with what we here see with respect to the large proportion of the perfect flowers being irregular, one genus alone out of the 38 heterostyled genera described in the previous chapters bears such flowers; yet all these genera are absolutely dependent on insects for their legitimate fertilisation. I know not how to account for this difference in the proportion of the plants bearing regular and irregular flowers in the two classes, unless it be that the heterostyled flowers are already so well adapted for cross-fertilisation, through the position of their stamens and pistils and the difference in power of their two or three kinds of pollen, that any additional adaptation, namely, through the flowers being made irregular, has been rendered superfluous.
Although cleistogamic flowers never fail to yield a large number of seeds, yet the plants bearing them usually produce perfect flowers, either simultaneously or more commonly at a different period; and these are adapted for or admit of cross-fertilisation. From the cases given of the two Indian species of Viola, which produced in this country during several years only cleistogamic flowers, and of the numerous plants of Vandellia and of some plants of Ononis which behaved during one whole season in the same manner, it appears rash to infer from such cases as that of Salvia cleistogama not having produced perfect flowers during five years in Germany (8/31. Dr. Ascherson 'Botanische Zeitung' 1871 page 555.), and of an Aspicarpa not having done so during several years in Paris, that these plants would not bear perfect flowers in their native homes. Von Mohl and several other botanists have repeatedly insisted that as a general rule the perfect flowers produced by cleistogamic plants are sterile; but it has been shown under the head of the several species that this is not the case. The perfect flowers Viola are indeed sterile unless they are visited by bees; but when thus visited they yield the full number of seeds. As far as I have been able to discover there is only one absolute exception to the rule that the perfect flowers are fertile, namely, that of Voandzeia; and in this case we should remember that cultivation often affects injuriously the reproductive organs. Although the perfect flowers of Leersia sometimes yield seeds, yet this occurs so rarely, as far as hitherto observed, that it practically forms a second exception to the rule.
As cleistogamic flowers are invariably fertilised, and as they are produced in large numbers, they yield altogether a much larger supply of seeds than do the perfect flowers on the same plant. But the latter flowers will occasionally be cross-fertilised, and their offspring will thus be invigorated, as we may infer from a wide-spread analogy. But of such invigoration I have only a small amount of direct evidence: two crossed seedlings of Ononis minutissima were put into competition with two seedlings raised from cleistogamic flowers; they were at first all of equal height; the crossed were then slightly beaten; but on the following year they showed the usual superiority of their class, and were to the self-fertilised plants of cleistogamic origin as 100 to 88 in mean height. With Vandellia twenty crossed plants exceeded in height twenty plants raised from cleistogamic seeds only by a little, namely, in the ratio of 100 to 94.
It is a natural inquiry how so many plants belonging to various very distinct families first came to have the development of their flowers arrested, so as ultimately to become cleistogamic. That a passage from the one state to the other is far from difficult is shown by the many recorded cases of gradations between the two states on the same plant, in Viola, Oxalis, Biophytum, Campanula, etc. In the several species of Viola the various parts of the flowers have also been modified in very different degrees. Those plants which in their own country produce flowers of full or nearly full size, but never expand (as with Thelymitra), and yet set fruit, might easily be rendered cleistogamic. Lathyrus nissolia seems to be in an incipient transitional state, as does Drosera Anglica, the flowers of which are not perfectly closed. There is good evidence that flowers sometimes fail to expand and are somewhat reduced in size, owing to exposure to unfavourable conditions, but still retain their fertility unimpaired. Linnaeus observed in 1753 that the flowers on several plants brought from Spain and grown at Upsala did not show any corolla and yet produced seeds. Asa Gray has seen flowers on exotic plants in the Northern United States which never expanded and yet fruited. With certain English plants, which