Several distinguished botanists and good practical judges believe that long- continued propagation by cuttings, runners, tubers, bulbs, etc., independently of any excessive development of these parts, is the cause of many plants failing to produce flowers, or producing only barren flowers,--it is as if they had lost the habit of s.e.xual generation. (18/109. G.o.dron 'De l'Espece'

tome 2 page 106; Herbert on Crocus in 'Journal of Hort. Soc.' volume 1 1846 page 254: Dr. Wight, from what he has seen in India, believes in this view; 'Madras Journal of Lit. and Science' volume 4 1836 page 61.) That many plants when thus propagated are sterile there can be no doubt, but as to whether the long continuance of this form of propagation is the actual cause of their sterility, I will not venture, from the want of sufficient evidence, to express an opinion.

That plants may be propagated for long periods by buds, without the aid of s.e.xual generation, we may safely infer from this being the case with many plants which must have long survived in a state of nature. As I have had occasion before to allude to this subject, I will here give such cases as I have collected. Many alpine plants ascend mountains beyond the height at which they can produce seed. (18/110. Wahlenberg specifies eight species in this state on the Lapland Alps: see Appendix to Linnaeus 'Tour in Lapland'

translated by Sir J.E. Smith volume 2 pages 274-280.) Certain species of Poa and Festuca, when growing on mountain-pastures, propagate themselves, as I hear from Mr. Bentham, almost exclusively by bulblets. Kalm gives a more curious instance (18/111. 'Travels in North America' English translation volume 3 page 175.) of several American trees, which grow so plentifully in marshes or in thick woods, that they are certainly well adapted for these stations, yet scarcely ever produce seeds; but when accidentally growing on the outside of the marsh or wood, are loaded with seed. The common ivy is found in Northern Sweden and Russia, but flowers and fruits only in the southern provinces. The Acorus calamus extends over a large portion of the globe, but so rarely perfects fruit that this has been seen only by a few botanists; according to Caspary, all its pollen-grains are in a worthless condition. (18/112. With respect to the ivy and Acorus see Dr. Broomfield in the 'Phytologist' volume 3 page 376. Also Lindley and Vaucher on the Acorus and see Caspary as below.) The Hyperic.u.m calycinum, which propagates itself so freely in our shrubberies by rhizomes, and is naturalised in Ireland, blossoms profusely, but rarely sets any seed, and this only during certain years; nor did it set any when fertilised in my garden by pollen from plants growing at a distance. The Lysimachia nummularia, which is furnished with long runners, so seldom produces seed-capsules, that Prof. Decaisne (18/113. 'Annal. des Sc.

Nat.' 3rd series Zool. tome 4 page 280. Prof. Decaisne refers also to a.n.a.logous cases with mosses and lichens near Paris.), who has especially attended to this plant, has never seen it in fruit. The Carex rigida often fails to perfect its seed in Scotland, Lapland, Greenland, Germany, and New Hampshire in the United States. (18/114. Mr. Tuckermann in Silliman's 'American Journal of Science' volume 65 page 1.) The periwinkle (Vinca minor), which spreads largely by runners, is said scarcely ever to produce fruit in England (18/115. Sir J.E. Smith 'English Flora' volume 1 page 339.); but this plant requires insect-aid for its fertilisation, and the proper insects may be absent or rare. The Jussiaea grandiflora has become naturalised in Southern France, and has spread by its rhizomes so extensively as to impede the navigation of the waters, but never produces fertile seed. (18/116. G.

Planchon 'Flora de Montpellier' 1864 page 20.) The horse-radish (Cochleria armoracia) spreads pertinaciously and is naturalised in various parts of Europe; though it bears flowers, these rarely produce capsules: Professor Caspary informs me that he has watched this plant since 1851, but has never seen its fruit; 65 per cent of its pollen-grains are bad. The common Ranunculus ficaria rarely bears seed in England, France, or Switzerland; but in 1863 I observed seeds on several plants growing near my house. (18/117. On the non-production of seeds in England see Mr. Crocker in 'Gardener's Weekly Magazine' 1852 page 70; Vaucher 'Hist. Phys. Plantes d'Europe' tome 1 page 33; Lecoq 'Geograph. Bot. d'Europe' tome 4 page 466; Dr. D. Clos in 'Annal. des Sc. Nat.' 3rd series Bot. tome 17 1852 page 129: this latter author refers to other a.n.a.logous cases. See more especially on this plant and on other allied cases Prof. Caspary "Die Nuphar" 'Abhand. Naturw. Gesellsch. zu Halle' b. 11 1870 page 40, 78.) Other cases a.n.a.logous with the foregoing could be given; for instance, some kinds of mosses and lichens have never been seen to fructify in France.

Some of these endemic and naturalised plants are probably rendered sterile from excessive multiplication by buds, and their consequent incapacity to produce and nourish seed. But the sterility of others more probably depends on the peculiar conditions under which they live, as in the case of the ivy in the northern part of Europe, and of the trees in the swamps of the United States; yet these plants must be in some respects eminently well adapted for the stations which they occupy, for they hold their places against a host of compet.i.tors.]

Finally, the high degree of sterility which often accompanies the doubling of flowers, or an excessive development of fruit, seldom supervenes at once. An incipient tendency is observed, and continued selection completes the result.

The view which seems the most probable, and which connects together all the foregoing facts and brings them within our present subject, is, that changed and unnatural conditions of life first give a tendency to sterility; and in consequence of this, the organs of reproduction being no longer able fully to perform their proper functions, a supply of organised matter, not required for the development of the seed, flows either into these organs and renders them foliaceous, or into the fruit, stems, tubers, etc., increasing their size and succulency. But it is probable that there exists, independently of any incipient sterility, an antagonism between the two forms of reproduction, namely, by seed and buds, when either is carried to an extreme degree. That incipient sterility plays an important part in the doubling of flowers, and in the other cases just specified, I infer chiefly from the following facts. When fertility is lost from a wholly different cause, namely, from hybridism, there is a strong tendency, as Gartner (18/118. 'b.a.s.t.a.r.derzeugung' s. 565. Kolreuter 'Dritte Fortsetzung' s. 73, 87, 119) also shows that when two species, one single and the other double, are crossed, the hybrids are apt to be extremely double.) affirms, for flowers to become double, and this tendency is inherited. Moreover, it is notorious that with hybrids the male organs become sterile before the female organs, and with double flowers the stamens first become foliaceous. This latter fact is well shown by the male flowers of dioecious plants, which, according to Gallesio (18/119. 'Teoria della Riproduzione Veg.' 1816 page 73.) first become double. Again, Gartner (18/120.

'b.a.s.t.a.r.derzeugung' s. 573.) often insists that the flowers of even utterly sterile hybrids, which do not produce any seed, generally yield perfect capsules or fruit,--a fact which has likewise been repeatedly observed by Naudin with the Cucurbitaceae; so that the production of fruit by plants rendered sterile through any cause is intelligible. Kolreuter has also expressed his unbounded astonishment at the size and development of the tubers in certain hybrids; and all experimentalists (18/121. Ibid s. 527.) have remarked on the strong tendency in hybrids to increase by roots, runners, and suckers. Seeing that hybrid plants, which from their nature are more or less sterile, thus tend to produce double flowers; that they have the parts including the seed, that is the fruit, perfectly developed, even when containing no seed; that they sometimes yield gigantic roots; that they almost invariably tend to increase largely by suckers and other such means;--seeing this, and knowing, from the many facts given in the earlier parts of this chapter, that almost all organic beings when exposed to unnatural conditions tend to become more or less sterile, it seems much the most probable view that with cultivated plants sterility is the exciting cause, and double flowers, rich seedless fruit, and in some cases largely-developed organs of vegetation, etc., are the indirect results--these results having been in most cases largely increased through continued selection by man.

CHAPTER 2.XIX.

SUMMARY OF THE FOUR LAST CHAPTERS, WITH REMARKS ON HYBRIDISM.

ON THE EFFECTS OF CROSSING.

THE INFLUENCE OF DOMESTICATION ON FERTILITY.

CLOSE INTERBREEDING.

GOOD AND EVIL RESULTS FROM CHANGED CONDITIONS OF LIFE.

VARIETIES WHEN CROSSED NOT INVARIABLY FERTILE.

ON THE DIFFERENCE IN FERTILITY BETWEEN CROSSED SPECIES AND VARIETIES.

CONCLUSIONS WITH RESPECT TO HYBRIDISM.

LIGHT THROWN ON HYBRIDISM BY THE ILLEGITIMATE PROGENY OF HETEROSTYLED PLANTS.

STERILITY OF CROSSED SPECIES DUE TO DIFFERENCES CONFINED TO THE REPRODUCTIVE SYSTEM.

NOT ACc.u.mULATED THROUGH NATURAL SELECTION.

REASONS WHY DOMESTIC VARIETIES ARE NOT MUTUALLY STERILE.

TOO MUCH STRESS HAS BEEN LAID ON THE DIFFERENCE IN FERTILITY BETWEEN CROSSED SPECIES AND CROSSED VARIETIES.

CONCLUSION.

It was shown in the fifteenth chapter that when individuals of the same variety, or even of a distinct variety, are allowed freely to intercross, uniformity of character is ultimately acquired. Some few characters, however, are incapable of fusion, but these are unimportant, as they are often of a semi-monstrous nature, and have suddenly appeared. Hence, to preserve our domesticated breeds true, or to improve them by methodical selection, it is obviously necessary that they should be kept separate. Nevertheless, a whole body of individuals may be slowly modified, through unconscious selection, as we shall see in a future chapter, without separating them into distinct lots.

Domestic races have often been intentionally modified by one or two crosses, made with some allied race, and occasionally even by repeated crosses with very distinct races; but in almost all such cases, long-continued and careful selection has been absolutely necessary, owing to the excessive variability of the crossed offspring, due to the principle of reversion. In a few instances, however, mongrels have retained a uniform character from their first production.

When two varieties are allowed to cross freely, and one is much more numerous than the other, the former will ultimately absorb the latter. Should both varieties exist in nearly equal numbers, it is probable that a considerable period would elapse before the acquirement of a uniform character; and the character ultimately acquired would largely depend on prepotency of transmission and on the conditions of life; for the nature of these conditions would generally favour one variety more than another, so that a kind of natural selection would come into play. Unless the crossed offspring were slaughtered by man without the least discrimination, some degree of unmethodical selection would likewise come into action. From these several considerations we may infer, that when two or more closely allied species first came into the possession of the same tribe, their crossing will not have influenced, in so great a degree as has often been supposed, the character of the offspring in future times; although in some cases it probably has had a considerable effect.

Domestication, as a general rule, increases the prolificness of animals and plants. It eliminates the tendency to sterility which is common to species when first taken from a state of nature and crossed. On this latter head we have no direct evidence; but as our races of dogs, cattle, pigs etc., are almost certainly descended from aboriginally distinct stocks, and as these races are now fully fertile together, or at least incomparably more fertile than most species when crossed, we may with entire confidence accept this conclusion.

Abundant evidence has been given that crossing adds to the size, vigour, and fertility of the offspring. This holds good when there has been no previous close interbreeding. It applies to the individuals of the same variety but belonging to different families, to distinct varieties, sub-species, and even to species. In the latter case, though size is gained, fertility is lost; but the increased size, vigour, and hardiness of many hybrids cannot be accounted for solely on the principle of compensation from the inaction of the reproductive system. Certain plants whilst growing under their natural conditions, others when cultivated, and others of hybrid origin, are completely self-impotent, though perfectly healthy; and such plants can be stimulated to fertility only by being crossed with other individuals of the same or of a distinct species.

On the other hand, long-continued close interbreeding between the nearest relations diminishes the const.i.tutional vigour, size, and fertility of the offspring; and occasionally leads to malformations, but not necessarily to general deterioration of form or structure. This failure of fertility shows that the evil results of interbreeding are independent of the augmentation of morbid tendencies common to both parents, though this augmentation no doubt is often highly injurious. Our belief that evil follows from close interbreeding rests to a certain extent on the experience of practical breeders, especially of those who have reared many animals of quickly propagating kinds; but it likewise rests on several carefully recorded experiments. With some animals close interbreeding may be carried on for a long period with impunity by the selection of the most vigorous and healthy individuals; but sooner or later evil follows. The evil, however, comes on so slowly and gradually that it easily escapes observation, but can be recognised by the almost instantaneous manner in which size, const.i.tutional vigour, and fertility are regained when animals that have long been interbred are crossed with a distinct family.

These two great cla.s.ses of facts, namely, the good derived from crossing, and the evil from close interbreeding, with the consideration of the innumerable adaptations throughout nature for compelling, or favouring, or at least permitting, the occasional union of distinct individuals, taken together, lead to the conclusion that it is a law of nature that organic beings shall not fertilise themselves for perpetuity. This law was first plainly hinted at in 1799, with respect to plants, by Andrew Knight (19/1. 'Transactions Phil.

Soc.' 1799 page 202. For Kolreuter see 'Mem. de l'Acad. de St.-Petersbourg'

tome 3 1809 published 1811 page 197. In reading C.K. Sprengel's remarkable work, 'Das entdeckte Geheimniss' etc. 1793, it is curious to observe how often this wonderfully acute observer failed to understand the full meaning of the structure of the flowers which he has so well described, from not always having before his mind the key to the problem, namely, the good derived from the crossing of distinct individual plants.) and, not long afterwards, that sagacious observer Kolreuter, after showing how well the Malvaceae are adapted for crossing, asks, "an id aliquid in recessu habeat, quod hujuscemodi flores nunquam proprio suo pulvere, sed semper eo aliarum su speciei impregnentur, merito quaritur? Certe natura nil facit frustra." Although we may demur to Kolreuter's saying that nature does nothing in vain, seeing how many rudimentary and useless organs there are, yet undoubtedly the argument from the innumerable contrivances, which favour crossing, is of the greatest weight. The most important result of this law is that it leads to uniformity of character in the individuals of the same species. In the case of certain hermaphrodites, which probably intercross only at long intervals of time, and with unis.e.xual animals inhabiting somewhat separated localities, which can only occasionally come into contact and pair, the greater vigour and fertility of the crossed offspring will ultimately tend to give uniformity of character.

But when we go beyond the limits of the same species, free intercrossing is barred by the law of sterility.

In searching for facts which might throw light on the cause of the good effects from crossing, and of the evil effects from close interbreeding, we have seen that, on the one hand, it is a widely prevalent and ancient belief, that animals and plants profit from slight changes in their condition of life; and it would appear that the germ, in a somewhat a.n.a.logous manner, is more effectually stimulated by the male element, when taken from a distinct individual, and therefore slightly modified in nature, than when taken from a male having the same identical const.i.tution. On the other hand, numerous facts have been given, showing that when animals are first subjected to captivity, even in their native land, and although allowed much liberty, their reproductive functions are often greatly impaired or quite annulled. Some groups of animals are more affected than others, but with apparently capricious exceptions in every group. Some animals never or rarely couple under confinement; some couple freely, but never or rarely conceive. The secondary male characters, the maternal functions and instincts, are occasionally affected. With plants, when first subjected to cultivation, a.n.a.logous facts have been observed. We probably owe our double flowers, rich seedless fruits, and in some cases greatly developed tubers, etc., to incipient sterility of the above nature combined with a copious supply of nutriment. Animals which have long been domesticated, and plants which have long been cultivated, can generally withstand, with unimpaired fertility, great changes in their conditions of life; though both are sometimes slightly affected. With animals the somewhat rare capacity of breeding freely under confinement, together with their utility, mainly determine the kinds which have been domesticated.

We can in no case precisely say what is the cause of the diminished fertility of an animal when first captured, or of a plant when first cultivated; we can only infer that it is caused by a change of some kind in the natural conditions of life. The remarkable susceptibility of the reproductive system to such changes,--a susceptibility not common to any other organ,--apparently has an important bearing on Variability, as we shall see in a future chapter.

It is impossible not to be struck with the double parallelism between the two cla.s.ses of facts just alluded to. On the one hand, slight changes in the conditions of life, and crosses between slightly modified forms or varieties, are beneficial as far as prolificness and const.i.tutional vigour are concerned.

On the other hand, changes in the conditions greater in degree, or of a different nature, and crosses between forms which have been slowly and greatly modified by natural means,--in other words, between species,--are highly injurious, as far as the reproductive system is concerned, and in some few instances as far as const.i.tutional vigour is concerned. Can this parallelism be accidental? Does it not rather indicate some real bond of connection? As a fire goes out unless it be stirred up, so the vital forces are always tending, according to Mr. Herbert Spencer, to a state of equilibrium, unless disturbed and renovated through the action of other forces.

In some few cases varieties tend to keep distinct, by breeding at different seasons, by great difference in size, or by s.e.xual preference. But the crossing of varieties, far from diminishing, generally adds to the fertility of the first union and of the mongrel offspring. Whether all the more widely distinct domestic varieties are invariably quite fertile when crossed, we do not positively know; much time and trouble would be requisite for the necessary experiments, and many difficulties occur, such as the descent of the various races from aboriginally distinct species, and the doubts whether certain forms ought to be ranked as species or varieties. Nevertheless, the wide experience of practical breeders proves that the great majority of varieties, even if some should hereafter prove not to be indefinitely fertile inter se, are far more fertile when crossed, than the vast majority of closely allied natural species. A few remarkable cases have, however, been given on the authority of excellent observers, showing that with plants certain forms, which undoubtedly must be ranked as varieties, yield fewer seeds when crossed than is natural to the parent-species. Other varieties have had their reproductive powers so far modified that they are either more or less fertile than their parents, when crossed with a distinct species.

Nevertheless, the fact remains indisputable that domesticated varieties, of animals and of plants, which differ greatly from one another in structure, but which are certainly descended from the same aboriginal species, such as the races of the fowl, pigeon, many vegetables, and a host of other productions, are extremely fertile when crossed; and this seems to make a broad and impa.s.sable barrier between domestic varieties and natural species. But, as I will now attempt to show, the distinction is not so great and overwhelmingly important as it at first appears.

ON THE DIFFERENCE IN FERTILITY BETWEEN VARIETIES AND SPECIES WHEN CROSSED.

This work is not the proper place for fully treating the subject of hybridism, and I have already given in my 'Origin of Species' a moderately full abstract.

I will here merely enumerate the general conclusions which may be relied on, and which bear on our present point.

FIRSTLY.

The laws governing the production of hybrids are identical, or nearly identical, in the animal and vegetable kingdoms.

SECONDLY.

The sterility of distinct species when first united, and that of their hybrid offspring, graduate, by an almost infinite number of steps, from zero, when the ovule is never impregnated and a seed-capsule is never formed, up to complete fertility. We can only escape the conclusion that some species are fully fertile when crossed, by determining to designate as varieties all the forms which are quite fertile. This high degree of fertility is, however, rare. Nevertheless, plants, which have been exposed to unnatural conditions, sometimes become modified in so peculiar a manner, that they are much more fertile when crossed with a distinct species than when fertilised by their own pollen. Success in effecting a first union between two species, and the fertility of their hybrids, depend in an eminent degree on the conditions of life being favourable. The innate sterility of hybrids of the same parentage and raised from the same seed-capsule often differs much in degree.

THIRDLY.

The degree of sterility of a first cross between two species does not always run strictly parallel with that of their hybrid offspring. Many cases are known of species which can be crossed with ease, but yield hybrids excessively sterile; and conversely some which can be crossed with great difficulty, but produce fairly fertile hybrids. This is an inexplicable fact, on the view that species have been specially endowed with mutual sterility in order to keep them distinct.

FOURTHLY.

The degree of sterility often differs greatly in two species when reciprocally crossed; for the first will readily fertilise the second; but the latter is incapable, after hundreds of trials, of fertilising the former. Hybrids produced from reciprocal crosses between the same two species likewise sometimes differ in their degree of sterility. These cases also are utterly inexplicable on the view of sterility being a special endowment.

FIFTHLY.

The degree of sterility of first crosses and of hybrids runs, to a certain extent, parallel with the general or systematic affinity of the forms which are united. For species belonging to distinct genera can rarely, and those belonging to distinct families can never, be crossed. The parallelism, however, is far from complete; for a mult.i.tude of closely allied species will not unite, or unite with extreme difficulty, whilst other species, widely different from one another, can be crossed with perfect facility. Nor does the difficulty depend on ordinary const.i.tutional differences, for annual and perennial plants, deciduous and evergreen trees, plants flowering at different seasons, inhabiting different stations, and naturally living under the most opposite climates, can often be crossed with ease. The difficulty or facility apparently depends exclusively on the s.e.xual const.i.tution of the species which are crossed; or on their s.e.xual elective affinity, i.e. Wahlverwandtschaft of Gartner. As species rarely or never become modified in one character, without being at the same time modified in many characters, and as systematic affinity includes all visible similarities and dissimilarities, any difference in s.e.xual const.i.tution between two species would naturally stand in more or less close relation with their systematic position.

SIXTHLY.

The sterility of species when first crossed, and that of hybrids, may possibly depend to a certain extent on distinct causes. With pure species the reproductive organs are in a perfect condition, whilst with hybrids they are often plainly deteriorated. A hybrid embryo which partakes of the const.i.tution of its father and mother is exposed to unnatural conditions, as long as it is nourished within the womb, or egg, or seed of the mother-form; and as we know that unnatural conditions often induce sterility, the reproductive organs of the hybrid might at this early age be permanently affected. But this cause has no bearing on the infertility of first unions. The diminished number of the offspring from first unions may often result, as is certainly sometimes the case, from the premature death of most of the hybrid embryos. But we shall immediately see that a law of an unknown nature apparently exists, which leads to the offspring from unions, which are infertile, being themselves more or less infertile; and this at present is all that can be said.

SEVENTHLY.

Hybrids and mongrels present, with the one great exception of fertility, the most striking accordance in all other respects; namely, in the laws of their resemblance to their two parents, in their tendency to reversion, in their variability, and in being absorbed through repeated crosses by either parent- form.

After arriving at these conclusions, I was led to investigate a subject which throws considerable light on hybridism, namely, the fertility of heterostyled or dimorphic and trimorphic plants, when illegitimately united. I have had occasion several times to allude to these plants, and I may here give a brief abstract of my observations. Several plants belonging to distinct orders present two forms, which exist in about equal numbers, and which differ in no respect except in their reproductive organs; one form having a long pistil with short stamens, the other a short pistil with long stamens; both with differently sized pollen-grains. With trimorphic plants there are three forms likewise differing in the lengths of their pistils and stamens, in the size and colour of the pollen-grains, and in some other respects; and as in each of the three forms there are two sets of stamens, there are altogether six sets of stamens and three kinds of pistils. These organs are so proportioned in length to one another that, in any two of the forms, half the stamens in each stand on a level with the stigma of the third form. Now I have shown, and the result has been confirmed by other observers, that, in order to obtain full fertility with these plants, it is necessary that the stigma of the one form should be fertilised by pollen taken from the stamens of corresponding height in the other form. So that with dimorphic species two unions, which may be called legitimate, are fully fertile, and two, which may be called illegitimate, are more or less infertile. With trimorphic species six unions are legitimate, or fully fertile, and twelve are illegitimate, or more or less infertile. (19/2. My observations 'On the Character and hybrid-like nature of the offspring from the illegitimate union of Dimorphic and Trimorphic Plants'

were published in the 'Journal of the Linnean Soc.' volume 10 page 393. The abstract here given is nearly the same with that which appeared in the 6th edition of my 'Origin of Species.')

The infertility which may be observed in various dimorphic and trimorphic plants, when illegitimately fertilised, that is, by pollen taken from stamens not corresponding in height with the pistil, differs much in degree, up to absolute and utter sterility; just in the same manner as occurs in crossing distinct species. As the degree of sterility in the latter case depends in an eminent degree on the conditions of life being more or less favourable, so I have found it with illegitimate unions. It is well known that if pollen of a distinct species be placed on the stigma of a flower, and its own pollen be afterwards, even after a considerable interval of time, placed on the same stigma, its action is so strongly prepotent that it generally annihilates the effect of the foreign pollen; so it is with the pollen of the several forms of the same species, for legitimate pollen is strongly prepotent over illegitimate pollen, when both are placed on the same stigma. I ascertained this by fertilising several flowers, first illegitimately, and twenty-four hours afterwards legitimately, with pollen taken from a peculiarly coloured variety, and all the seedlings were similarly coloured; this shows that the legitimate pollen, though applied twenty-four hours subsequently, had wholly destroyed or prevented the action of the previously applied illegitimate pollen. Again, as, in making reciprocal crosses between the same two species, there is occasionally a great difference in the result, so the same thing occurs with trimorphic plants; for instance, the mid-styled form of Lythrum salicaria could be illegitimately fertilised with the greatest ease by pollen from the longer stamens of the short-styled form, and yielded many seeds; but the short-styled form did not yield a single seed when fertilised by the longer stamens of the mid-styled form.

In all these respects the forms of the same undoubted species, when illegitimately united, behave in exactly the same manner as do two distinct species when crossed. This led me carefully to observe during four years many seedlings, raised from several illegitimate unions. The chief result is that these illegitimate plants, as they may be called, are not fully fertile. It is possible to raise from dimorphic species, both long-styled and short-styled illegitimate plants, and from trimorphic plants all three illegitimate forms.