Or, if the three poorest capsules be rejected, we get: 20 : 11 : 18.9 : 46 : 8.

The short-styled form of the common primrose LEGITIMATELY fertilised with pollen from the long-styled illegitimate purple- and yellow-flowered plants: 10 : 6 : 30.5 : 61 : 6.

If we compare the figures in this table with those given in the first chapter, showing the normal fertility of the common primrose, we shall see that the illegitimate purple- and yellow-flowered varieties are very sterile. For instance, 72 flowers were fertilised with their own pollen and produced only 11 good capsules; but by the standard they ought to have produced 48 capsules; and each of these ought to have contained on an average 52.2 seeds, instead of only 11.5 seeds. When these plants were illegitimately and legitimately fertilised with pollen from the common primrose, the average numbers were increased, but were far from attaining the normal standards. So it was when both forms of the common primrose were fertilised with pollen from these illegitimate plants; and this shows that their male as well as their female organs were in a deteriorated condition. The sterility of these plants was shown in another way, namely, by their not producing any capsules when the access of all insects (except such minute ones as Thrips) was prevented; for under these circ.u.mstances the common long-styled primrose produces a considerable number of capsules. There can, therefore, be no doubt that the fertility of these plants was greatly impaired.

The loss is not correlated with the colour of the flower; and it was to ascertain this point that I made so many experiments. As the parent-plant growing in Edinburgh was found by Mr. Scott to be in a high degree sterile, it may have transmitted a similar tendency to its offspring, independently of their illegitimate birth. I am, however, inclined to attribute some weight to the illegitimacy of their descent, both from the a.n.a.logy of other cases, and more especially from the fact that when the plants were LEGITIMATELY fertilised with pollen of the common primrose they yielded an average, as may be seen in the table, of only 5 more seeds than when ILLEGITIMATELY fertilised with the same pollen. Now we know that it is eminently characteristic of the illegitimate offspring of Primula Sinensis that they yield but few more seeds when legitimately fertilised than when fertilised with their own-form pollen.

Primula veris, Brit. Fl.

Var. officinalis of Linn., P. officinalis OF Jacq.

Seeds from the short-styled form of the cowslip fertilised with pollen from the same form germinate so badly that I raised from three successive sowings only fourteen plants, which consisted of nine short-styled and five long-styled plants. Hence the short-styled form of the cowslip, when self-fertilised, does not transmit the same form nearly so truly as does that of P. Sinensis. From the long-styled form, always fertilised with its own-form pollen, I raised in the first generation three long-styled plants,--from their seed 53 long-styled grandchildren,--from their seed 4 long-styled great-grandchildren,--from their seed 20 long-styled great-great-grandchildren,--and lastly, from their seed 8 long-styled and 2 short-styled great-great-great-grandchildren. In this last generation short-styled plants appeared for the first time in the course of the six generations,--the parent long-styled plant which was fertilised with pollen from another plant of the same form being counted as the first generation. Their appearance may be attributed to atavism. From two other long-styled plants, fertilised with their own-form pollen, 72 plants were raised, which consisted of 68 long-styled and 4 short-styled. So that altogether 162 plants were raised from illegitimately fertilised long-styled cowslips, and these consisted of 156 long-styled and 6 short-styled plants.

We will now turn to the fertility and powers of growth possessed by the illegitimate plants. From a short-styled plant, fertilised with its own-form pollen, one short-styled and two long-styled plants, and from a long-styled plant similarly fertilised three long-styled plants were at first raised. The fertility of these six illegitimate plants was carefully observed; but I must premise that I cannot give any satisfactory standard of comparison as far as the number of the seeds is concerned; for though I counted the seeds of many legitimate plants fertilised legitimately and illegitimately, the number varied so greatly during successive seasons that no one standard will serve well for illegitimate unions made during different seasons. Moreover the seeds in the same capsule frequently differ so much in size that it is scarcely possible to decide which ought to be counted as good seed. There remains as the best standard of comparison the proportional number of fertilised flowers which produce capsules containing any seed.

First, for the one illegitimate short-styled plant. In the course of three seasons 27 flowers were illegitimately fertilised with pollen from the same plant, and they yielded only a single capsule, which, however, contained a rather large number of seeds for a union of this nature, namely, 23. As a standard of comparison I may state that during the same three seasons 44 flowers borne by legitimate short-styled plants were self-fertilised, and yielded 26 capsules; so that the fact of the 27 flowers on the illegitimate plant having produced only one capsule proves how sterile it was. To show that the conditions of life were favourable, I will add that numerous plants of this and other species of Primula all produced an abundance of capsules whilst growing close by in the same soil with the present and following plants. The sterility of the above illegitimate short-styled plant depended on both the male and female organs being in a deteriorated condition. This was manifestly the case with the pollen; for many of the anthers were shrivelled or contabescent. Nevertheless some of the anthers contained pollen, with which I succeeded in fertilising some flowers on the illegitimate long-styled plants immediately to be described. Four flowers on this same short-styled plant were likewise LEGITIMATELY fertilised with pollen from one of the following long-styled plants; but only one capsule was produced, containing 26 seeds; and this is a very low number for a legitimate union.

With respect to the five illegitimate long-styled plants of the first generation, derived from the above self-fertilised short-styled and long-styled parents, their fertility was observed during the same three years. These five plants, when self-fertilised, differed considerably from one another in their degree of fertility, as was the case with the illegitimate long-styled plants of Lythrum salicaria; and their fertility varied much according to the season. I may premise, as a standard of comparison, that during the same years 56 flowers on legitimate long-styled plants of the same age and grown in the same soil, were fertilised with their own pollen, and yielded 27 capsules; that is, 48 per cent. On one of the five illegitimate long-styled plants 36 flowers were self- fertilised in the course of the three years, but they did not produce a single capsule. Many of the anthers on this plant were contabescent; but some seemed to contain sound pollen. Nor were the female organs quite impotent; for I obtained from a LEGITIMATE cross one capsule with good seed. On a second illegitimate long-styled plant 44 flowers were fertilised during the same years with their own pollen, but they produced only a single capsule. The third and fourth plants were in a very slight degree more productive. The fifth and last plant was decidedly more fertile; for 42 self-fertilised flowers yielded 11 capsules.

Altogether, in the course of the three years, no less than 160 flowers on these five illegitimate long-styled plants were fertilised with their own pollen, but they yielded only 22 capsules. According to the standard above given, they ought to have yielded 80 capsules. These 22 capsules contained on an average 15.1 seeds. I believe, subject to the doubts before specified, that with legitimate plants the average number from a union of this nature would have been above 20 seeds. Twenty-four flowers on these same five illegitimate long-styled plants were legitimately fertilised with pollen from the above-described illegitimate short-styled plant, and produced only 9 capsules, which is an extremely small number for a legitimate union. These 9 capsules, however, contained an average of 38 apparently good seeds, which is as large a number as legitimate plants sometimes yield. But this high average was almost certainly false; and I mention the case for the sake of showing the difficulty of arriving at a fair result; for this average mainly depended on two capsules containing the extraordinary numbers of 75 and 56 seeds; these seeds, however, though I felt bound to count them, were so poor that, judging from trials made in other cases, I do not suppose that one would have germinated; and therefore they ought not to have been included. Lastly, 20 flowers were legitimately fertilised with pollen from a legitimate plant, and this increased their fertility; for they produced 10 capsules. Yet this is but a very small proportion for a legitimate union.

There can, therefore, be no doubt that these five long-styled plants and the one short-styled plant of the first illegitimate generation were extremely sterile.

Their sterility was shown, as in the case of hybrids, in another way, namely, by their flowering profusely, and especially by the long endurance of the flowers.

For instance, I fertilised many flowers on these plants, and fifteen days afterwards (namely on March 22nd) I fertilised numerous long-styled and short- styled flowers on common cowslips growing close by. These latter flowers, on April 8th, were withered, whilst most of the illegitimate flowers remained quite fresh for several days subsequently; so that some of these illegitimate plants, after being fertilised, remained in full bloom for above a month.

We will now turn to the fertility of the 53 illegitimate long-styled grandchildren, descended from the long-styled plant which was first fertilised with its own pollen. The pollen in two of these plants included a mult.i.tude of small and shrivelled grains. Nevertheless they were not very sterile; for 25 flowers, fertilised with their own pollen, produced 15 capsules, containing an average of 16.3 seeds. As already stated, the probable average with legitimate plants for a union of this nature is rather above 20 seeds. These plants were remarkably healthy and vigorous, as long as they were kept under highly favourable conditions in pots in the greenhouse; and such treatment greatly increases the fertility of the cowslip. When these same plants were planted during the next year (which, however, was an unfavourable one), out of doors in good soil, 20 self-fertilised flowers produced only 5 capsules, containing extremely few and wretched seeds.

Four long-styled great-grandchildren were raised from the self-fertilised grandchildren, and were kept under the same highly favourable conditions in the greenhouse; 10 of their flowers were fertilised with own-form pollen and yielded the large proportion of 6 capsules, containing on an average 18.7 seeds. From these seeds 20 long-styled great-great-grandchildren were raised, which were likewise kept in the greenhouse. Thirty of their flowers were fertilised with their own pollen and yielded 17 capsules, containing on an average no less than 32, mostly fine seeds. It appears, therefore, that the fertility of these plants of the fourth illegitimate generation, as long as they were kept under highly favourable conditions, had not decreased, but had rather increased. The result, however, was widely different when they were planted out of doors in good soil, where other cowslips grew vigorously and were completely fertile; for these illegitimate plants now became much dwarfed in stature and extremely sterile, notwithstanding that they were exposed to the visits of insects, and must have been legitimately fertilised by the surrounding legitimate plants. A whole row of these plants of the fourth illegitimate generation, thus freely exposed and legitimately fertilised, produced only 3 capsules, containing on an average only 17 seeds. During the ensuing winter almost all these plants died, and the few survivors were miserably unhealthy, whilst the surrounding legitimate plants were not in the least injured.

The seeds from the great-great-grandchildren were sown, and 8 long-styled and 2 short-styled plants of the fifth illegitimate generation raised. These whilst still in the greenhouse produced smaller leaves and shorter flower-stalks than some legitimate plants with which they grew in compet.i.tion; but it should be observed that the latter were the product of a cross with a fresh stock,--a circ.u.mstance which by itself would have added much to their vigour. (5/11. For full details of this experiment, see my 'Effects of Cross and Self- fertilisation' 1876 page 220.) When these illegitimate plants were transferred to fairly good soil out of doors, they became during the two following years much more dwarfed in stature and produced very few flower-stems; and although they must have been legitimately fertilised by insects, they yielded capsules, compared with those produced by the surrounding legitimate plants, in the ratio only of 5 to 100! It is therefore certain that illegitimate fertilisation, continued during successive generations, affects the powers of growth and fertility of P. veris to an extraordinary degree; more especially when the plants are exposed to ordinary conditions of life, instead of being protected in a greenhouse.

[EQUAL-STYLED RED VARIETY OF Primula veris.

Mr. Scott has described a plant of this kind growing in the Botanic Garden of Edinburgh. (5/12. 'Proceedings of the Linnean Society' volume 8 1864 page 105.) He states that it was highly self-fertile, although insects were excluded; and he explains this fact by showing, first, that the anthers and stigma are in close apposition, and that the stamens in length, position and size of their pollen-grains resemble those of the short-styled form, whilst the pistil resembles that of the long-styled form both in length and in the structure of the stigma. Hence the self-union of this variety is, in fact, a legitimate union, and consequently is highly fertile. Mr. Scott further states that this variety yielded very few seeds when fertilised by either the long- or short- styled common cowslip, and, again, that both forms of the latter, when fertilised by the equal-styled variety, likewise produced very few seeds. But his experiments with the cowslip were few, and my results do not confirm his in any uniform manner.

I raised twenty plants from self-fertilised seed sent me by Mr. Scott; and they all produced red flowers, varying slightly in tint. Of these, two were strictly long-styled both in structure and in function; for their reproductive powers were tested by crosses with both forms of the common cowslip. Six plants were equal-styled; but on the same plant the pistil varied a good deal in length during different seasons. This was likewise the case, according to Mr. Scott, with the parent-plant. Lastly, twelve plants were in appearance short-styled; but they varied much more in the length of their pistils than ordinary short- styled cowslips, and they differed widely from the latter in their powers of reproduction. Their pistils had become short-styled in structure, whilst remaining long-styled in function. Short-styled cowslips, when insects are excluded, are extremely barren: for instance, on one occasion six fine plants produced only about 50 seeds (that is, less than the product of two good capsules), and on another occasion not a single capsule. Now, when the above twelve apparently short-styled seedlings were similarly treated, nearly all produced a great abundance of capsules, containing numerous seeds, which germinated remarkably well. Moreover three of these plants, which during the first year were furnished with quite short pistils, on the following year produced pistils of extraordinary length. The greater number, therefore, of these short-styled plants could not be distinguished in function from the equal- styled variety. The anthers in the six equal-styled and in the apparently twelve short-styled plants were seated high up in the corolla, as in the true short- styled cowslip; and the pollen-grains resembled those of the same form in their large size, but were mingled with a few shrivelled grains. In function this pollen was identical with that of the short-styled cowslip; for ten long-styled flowers of the common cowslip, legitimately fertilised with pollen from a true equal-styled variety, produced six capsules, containing on an average 34.4 seeds; whilst seven capsules on a short-styled cowslip illegitimately fertilised with pollen from the equal-styled variety, yielded an average of only 14.5 seeds.

As the equal-styled plants differ from one another in their powers of reproduction, and as this is an important subject, I will give a few details with respect to five of them. First, an equal-styled plant, protected from insects (as was done in all the following cases, with one stated exception), spontaneously produced numerous capsules, five of which gave an average of 44.8 seeds, with a maximum in one capsule of 57. But six capsules, the product of fertilisation with pollen from a short-styled cowslip (and this is a legitimate union), gave an average of 28.5 seeds, with a maximum of 49; and this is a much lower average than might have been expected. Secondly, nine capsules from another equal-styled plant, which had not been protected from insects, but probably was self-fertilised, gave an average of 45.2 seeds, with a maximum of 58. Thirdly, another plant which had a very short pistil in 1865, produced spontaneously many capsules, six of which contained an average of 33.9 seeds, with a maximum of 38. In 1866 this same plant had a pistil of wonderful length; for it projected quite above the anthers, and the stigma resembled that of the long-styled form. In this condition it produced spontaneously a vast number of fine capsules, six of which contained almost exactly the same average number as before, namely 34.3, with a maximum of 38. Four flowers on this plant, legitimately fertilised with pollen from a short-styled cowslip, yielded capsules with an average of 30.2 seeds. Fourthly another short-styled plant spontaneously produced in 1865 an abundance of capsules, ten of which contained an average of 35.6 seeds, with a maximum of 54. In 1866 this same plant had become in all respects long-styled, and ten capsules gave almost exactly the same average as before, namely 35.1 seeds, with a maximum of 47. Eight flowers on this plant, legitimately fertilised with pollen from a short-styled cowslip, produced six capsules, with the high average of 53 seeds, and the high maximum of 67. Eight flowers were also fertilised with pollen from a long-styled cowslip (this being an illegitimate union), and produced seven capsules, containing an average of 24.4 seeds, with a maximum of 32. The fifth and last plant remained in the same condition during both years: it had a pistil rather longer than that of the true short-styled form, with the stigma smooth, as it ought to be in this form, but abnormal in shape, like a much-elongated inverted cone. It produced spontaneously many capsules, five of which, in 1865, gave an average of only 15.6 seeds; and in 1866 ten capsules still gave an average only a little higher, namely of 22.1, with a maximum of 30. Sixteen flowers were fertilised with pollen from a long-styled cowslip, and produced 12 capsules, with an average of 24.9 seeds, and a maximum of 42. Eight flowers were fertilised with pollen from a short-styled cowslip, but yielded only two capsules, containing 18 and 23 seeds. Hence this plant, in function and partially in structure, was in an almost exactly intermediate state between the long-styled and short-styled form, but inclining towards the short-styled; and this accounts for the low average of seeds which it produced when spontaneously self-fertilised.

The foregoing five plants thus differ much from one another in the nature of their fertility. In two individuals a great difference in the length of the pistil during two succeeding years made no difference in the number of seeds produced. As all five plants possessed the male organs of the short-styled form in a perfect state, and the female organs of the long-styled form in a more or less complete state, they spontaneously produced a surprising number of capsules, which generally contained a large average of remarkably fine seeds.

With ordinary cowslips LEGITIMATELY FERTILISED, I once obtained from plants cultivated in the greenhouse the high average, from seven capsules, of 58.7 seeds, with a maximum in one capsule of 87 seeds; but from plants grown out of doors I never obtained a higher average than 41 seeds. Now two of the equal- styled plants, grown out of doors and spontaneously SELF-FERTILISED, gave averages of 44 and 45 seeds; but this high fertility may perhaps be in part attributed to the stigma receiving pollen from the surrounding anthers at exactly the right period. Two of these plants, fertilised with pollen from a short-styled cowslip (and this in fact is a legitimate union), gave a lower average than when self-fertilised. On the other hand, another plant, when similarly fertilised by a cowslip, yielded the unusually high average of 53 seeds, with a maximum of 67. Lastly, as we have just seen, one of these plants was in an almost exactly intermediate condition in its female organs between the long- and short-styled forms, and consequently, when self-fertilised, yielded a low average of seed. If we add together all the experiments which I made on the equal-styled plants, 41 spontaneously self-fertilised capsules (insects having been excluded) gave an average of 34 seeds, which is exactly the same number as the parent-plant yielded in Edinburgh. Thirty-four flowers, fertilised with pollen from the short-styled cowslip (and this is an a.n.a.logous union), produced 17 capsules, containing an average of 33.8 seeds. It is a rather singular circ.u.mstance, for which I cannot account, that 20 flowers, artificially fertilised on one occasion with pollen from the same plants yielded only ten capsules, containing the low average of 26.7 seeds.

As bearing on inheritance, it may be added that 72 seedlings were raised from one of the red-flowered, strictly equal-styled, self-fertilised plants descended from the similarly characterised Edinburgh plant. These 72 plants were therefore grandchildren of the Edinburgh plant, and they all bore, as in the first generation, red flowers, with the exception of one plant, which reverted in colour to the common cowslip. In regard to structure, nine plants were truly long-styled and had their stamens seated low down in the corolla in the proper position; the remaining 63 plants were equal-styled, though the stigma in about a dozen of them stood a little below the anthers. We thus see that the anomalous combination in the same flower, of the male and female s.e.xual organs which properly exist in the two distinct forms, was inherited with much force. Thirty- six seedlings were also raised from long and short-styled common cowslips, crossed with pollen from the equal-styled variety. Of these plants one alone was equal-styled, 20 were short-styled, but with the pistil in three of them rather too long, and the remaining 15 were long-styled. In this case we have an ill.u.s.tration of the difference between simple inheritance and prepotency of transmission; for the equal-styled variety, when self-fertilised, transmits its character, as we have just seen, with much force, but when crossed with the common cowslip cannot withstand the greater power of transmission of the latter.

PULMONARIA.

I have little to say on this genus. I obtained seeds of P. officinalis from a garden where the long-styled form alone grew, and raised 11 seedlings, which were all long-styled. These plants were named for me by Dr. Hooker. They differed, as has been shown, from the plants belonging to this species which in Germany were experimented on by Hildebrand (5/13. 'Botanische Zeitung' 1865 page 13.); for he found that the long-styled form was absolutely sterile with its own pollen, whilst my long-styled seedlings and the parent-plants yielded a fair supply of seed when self-fertilised. Plants of the long-styled form of Pulmonaria angustifolia were, like Hildebrand's plants, absolutely sterile with their own pollen, so that I could never procure a single seed. On the other hand, the short-styled plants of this species, differently from those of P.

officinalis, were fertile with their own pollen in a quite remarkable degree for a heterostyled plant. From seeds carefully self-fertilised I raised 18 plants, of which 13 proved short-styled and 5 long-styled.

Polygonum f.a.gopyrum.

From flowers on long-styled plants fertilised illegitimately with pollen from the same plant, 49 seedlings were raised, and these consisted of 45 long-styled and 4 short-styled. From flowers on short-styled plants illegitimately fertilised with pollen from the same plant 33 seedlings were raised, and these consisted of 20 short-styled and 13 long-styled. So that the usual rule of illegitimately fertilised long-styled plants tending much more strongly than short-styled plants to reproduce their own form here holds good. The illegitimate plants derived from both forms flowered later than the legitimate, and were to the latter in height as 69 to 100. But as these illegitimate plants were descended from parents fertilised with their own pollen, whilst the legitimate plants were descended from parents crossed with pollen from a distinct individual, it is impossible to know how much of their difference in height and period of flowering, is due to the illegitimate birth of the one set, and how much to the other set being the product of a cross between distinct plants.]

CONCLUDING REMARKS ON THE ILLEGITIMATE OFFSPRING OF HETEROSTYLED TRIMORPHIC AND DIMORPHIC PLANTS.

It is remarkable how closely and in how many points illegitimate unions between the two or three forms of the same heterostyled species, together with their illegitimate offspring, resemble hybrid unions between distinct species together with their hybrid offspring. In both cases we meet with every degree of sterility, from very slightly lessened fertility to absolute barrenness, when not even a single seed-capsule is produced. In both cases the facility of effecting the first union is much influenced by the conditions to which the plants are exposed. (5/14. This has been remarked by many experimentalists in effecting crosses between distinct species; and in regard to illegitimate unions I have given in the first chapter a striking ill.u.s.tration in the case of Primula veris.) Both with hybrids and illegitimate plants the innate degree of sterility is highly variable in plants raised from the same mother-plant. In both cases the male organs are more plainly affected than the female; and we often find contabescent anthers enclosing shrivelled and utterly powerless pollen-grains.

The more sterile hybrids, as Max Wichura has well shown, are sometimes much dwarfed in stature, and have so weak a const.i.tution that they are liable to premature death (5/15. 'Die b.a.s.t.a.r.dbefruchtung im Pflanzenreich' 1865.); and we have seen exactly parallel cases with the illegitimate seedlings of Lythrum and Primula. Many hybrids are the most persistent and profuse flowerers, as are some illegitimate plants. When a hybrid is crossed by either pure parent-form, it is notoriously much more fertile than when crossed inter se or by another hybrid; so when an illegitimate plant is fertilised by a legitimate plant, it is more fertile than when fertilised inter se or by another illegitimate plant. When two species are crossed and they produce numerous seeds, we expect as a general rule that their hybrid offspring will be moderately fertile; but if the parent species produce extremely few seeds, we expect that the hybrids will be very sterile. But there are marked exceptions, as shown by Gartner, to these rules.

So it is with illegitimate unions and illegitimate offspring. Thus the mid- styled form of Lythrum salicaria, when illegitimately fertilised with pollen from the longest stamens of the short-styled form, produced an unusual number of seeds; and their illegitimate offspring were not at all, or hardly at all, sterile. On the other hand, the illegitimate offspring from the long-styled form, fertilised with pollen from the shortest stamens of the same form, yielded few seeds, and the illegitimate offspring thus produced were very sterile; but they were more sterile than might have been expected relatively to the difficulty of effecting the union of the parent s.e.xual elements. No point is more remarkable in regard to the crossing of species than their unequal reciprocity. Thus species A will fertilise B with the greatest ease; but B will not fertilise A after hundreds of trials. We have exactly the same case with illegitimate unions; for the mid-styled Lythrum salicaria was easily fertilised by pollen from the longest stamens of the short-styled form, and yielded many seeds; but the latter form did not yield a single seed when fertilised by the longest stamens of the mid-styled form.

Another important point is prepotency. Gartner has shown that when a species is fertilised with pollen from another species, if it be afterwards fertilised with its own pollen, or with that of the same species, this is so prepotent over the foreign pollen that the effect of the latter, though placed on the stigma some time previously, is entirely destroyed. Exactly the same thing occurs with the two forms of a heterostyled species. Thus several long-styled flowers of Primula veris were fertilised illegitimately with pollen from another plant of the same form, and twenty-four hours afterwards legitimately with pollen from a short- styled dark-red polyanthus which is a variety of P. veris; and the result was that every one of the thirty seedlings thus raised bore flowers more or less red, showing plainly how prepotent the legitimate pollen from a short-styled plant was over the illegitimate pollen from a long-styled plant.

In all the several foregoing points the parallelism is wonderfully close between the effects of illegitimate and hybrid fertilisation. It is hardly an exaggeration to a.s.sert that seedlings from an illegitimately fertilised heterostyled plant are hybrids formed within the limits of one and the same species. This conclusion is important, for we thus learn that the difficulty in s.e.xually uniting two organic forms and the sterility of their offspring, afford no sure criterion of so-called specific distinctness. If any one were to cross two varieties of the same form of Lythrum or Primula for the sake of ascertaining whether they were specifically distinct, and he found that they could be united only with some difficulty, that their offspring were extremely sterile, and that the parents and their offspring resembled in a whole series of relations crossed species and their hybrid offspring, he might maintain that his varieties had been proved to be good and true species; but he would be completely deceived. In the second place, as the forms of the same trimorphic or dimorphic heterostyled species are obviously identical in general structure, with the exception of the reproductive organs, and as they are identical in general const.i.tution (for they live under precisely the same conditions), the sterility of their illegitimate unions and that of their illegitimate offspring, must depend exclusively on the nature of the s.e.xual elements and on their incompatibility for uniting in a particular manner. And as we have just seen that distinct species when crossed resemble in a whole series of relations the forms of the same species when illegitimately united, we are led to conclude that the sterility of the former must likewise depend exclusively on the incompatible nature of their s.e.xual elements, and not on any general difference in const.i.tution or structure. We are, indeed, led to this same conclusion by the impossibility of detecting any differences sufficient to account for certain species crossing with the greatest ease, whilst other closely allied species cannot be crossed, or can be crossed only with extreme difficulty. We are led to this conclusion still more forcibly by considering the great difference which often exists in the facility of crossing reciprocally the same two species; for it is manifest in this case that the result must depend on the nature of the s.e.xual elements, the male element of the one species acting freely on the female element of the other, but not so in a reversed direction. And now we see that this same conclusion is independently and strongly fortified by the consideration of the illegitimate unions of trimorphic and dimorphic heterostyled plants. In so complex and obscure a subject as hybridism it is no slight gain to arrive at a definite conclusion, namely, that we must look exclusively to functional differences in the s.e.xual elements, as the cause of the sterility of species when first crossed and of their hybrid offspring. It was this consideration which led me to make the many observations recorded in this chapter, and which in my opinion make them worthy of publication.

CHAPTER VI.

CONCLUDING REMARKS ON HETEROSTYLED PLANTS.

The essential character of heterostyled plants.

Summary of the differences in fertility between legitimately and illegitimately fertilised plants.

Diameter of the pollen-grains, size of anthers and structure of stigma in the different forms.

Affinities of the genera which include heterostyled species.

Nature of the advantages derived from heterostylism.

The means by which plants became heterostyled.

Transmission of form.

Equal-styled varieties of heterostyled plants.

Final remarks.

In the foregoing chapters all the heterostyled plants known to me have been more or less fully described. Several other cases have been indicated, especially by Professor Asa Gray and Kuhn, in which the individuals of the same species differ in the length of their stamens and pistils (6/1. Asa Gray 'American Journal of Science' 1865 page 101 and elsewhere as already referred to. Kuhn 'Botanische Zeitung' 1867 page 67.); but as I have been often deceived by this character taken alone, it seems to me the more prudent course not to rank any species as heterostyled, unless we have evidence of more important differences between the forms, as in the diameter of the pollen-grains, or in the structure of the stigma. The individuals of many ordinary hermaphrodite plants habitually fertilise one another, owing to their male and female organs being mature at different periods, or to the structure of the parts, or to self-sterility, etc.; and so it is with many hermaphrodite animals, for instance, land-snails or earth-worms; but in all these cases any one individual can fully fertilise or be fertilised by any other individual of the same species. This is not so with heterostyled plants: a long-styled, mid-styled or short-styled plant cannot fully fertilise or be fertilised by any other individual, but only by one belonging to another form. Thus the essential character of plants belonging to the heterostyled cla.s.s is that the individuals are divided into two or three bodies, like the males and females of dioecious plants or of the higher animals, which exist in approximately equal numbers and are adapted for reciprocal fertilisation. The existence, therefore, of two or three bodies of individuals, differing from one another in the above more important characteristics, offers by itself good evidence that the species is heterostyled. But absolutely conclusive evidence can be derived only from experiments, and by finding that pollen must be applied from the one form to the other in order to ensure complete fertility.

In order to show how much more fertile each form is when legitimately fertilised with pollen from the other form (or in the case of trimorphic species, with the proper pollen from one of the two other forms) than when illegitimately fertilised with its own-form pollen, I will append Table 6.33 giving a summary of the results in all the cases. .h.i.therto ascertained. The fertility of the unions may be judged by two standards, namely, by the proportion of flowers which, when fertilised in the two methods, yield capsules, and by the average number of seeds per capsule. When there is a dash in the left hand column opposite to the name of the species, the proportion of the flowers which yielded capsules was not recorded.

TABLE 6.33. Fertility of the legitimate unions taken together, compared with that of the illegitimate unions together. The fertility of the legitimate unions, as judged by both standards, is taken as 100.

Column 1: Name of species.

Column 2: Illegitimate unions : proportional number of flowers which produced capsules.

Column 3: Illegitimate unions : average number of seeds per capsule.

Primula veris : 69 : 65.

Primula elatior : 27 : 75.

Primula vulgaris : 60 : 54.

Primula Sinensis : 84 : 63.

Primula Sinensis (second trial) : 0 : 53.

Primula Sinensis (Hildebrand) : 100 : 42.

Primula auricula (Scott) : 80 : 15.