Characters of all kinds are affected by graft hybridisation, in whatever way the grafting may have been effected. The plants thus raised yield tubers which partake of the widely different colours, form, state of surface, position and shape of the eye of the parents; and according to two careful observers they are also intermediate in certain const.i.tutional peculiarities. But we should bear in mind that in all the varieties of the potato, the tubers differ much more than any other part.

The potato affords the best evidence of the possibility of the formation of graft-hybrids, but we must not overlook the account given of the origin of the famous Cytisus adami by M. Adam, who had no conceivable motive for deception, and the exactly parallel account of the origin of the Bizzarria orange, namely by graft-hybridisation. Nor must the cases be undervalued in which different varieties or species of vines, hyacinths and roses, have been grafted together, and have yielded intermediate forms. It is evident that graft-hybrids can be made much more easily with some plants, as the potato, than with others, for instance our common fruit trees; for these latter have been grafted by the million during many centuries, and though the graft is often slightly affected, it is very doubtful whether this may not be accounted for, merely by a more or less free supply of nutriment.

Nevertheless, the cases above given seem to me to prove that under certain unknown conditions graft-hybridisation can be effected.

Herr Magnus a.s.serts with much truth that graft-hybrids resemble in all respects seminal hybrids, including their great diversity of character.

There is, however, a partial exception, inasmuch as the characters of the two parent forms are not often h.o.m.ogeneously blended together in graft- hybrids. They much more commonly appear in a segregated condition,--that is, in segments either at first, or subsequently through reversion. It would seem that the reproductive elements are not so completely blended by grafting as by s.e.xual generation. But segregation of this kind occurs by no means rarely, as will be immediately shown, in seminal hybrids. Finally it must, I think, be admitted that we learn from the foregoing cases a highly important physiological fact, namely, that the elements that go to the production of a new being, are not necessarily formed by the male and female organs. They are present in the cellular tissue in such a state that they can unite without the aid of the s.e.xual organs, and thus give rise to a new bud partaking of the characters of the two parent-forms.

ON THE SEGREGATION OF THE PARENTAL CHARACTERS IN SEMINAL HYBRIDS BY BUD- VARIATION.

I will now give a sufficient number of cases to show that segregation of this kind, namely, by buds, may occur in ordinary hybrids raised from seed.

[Hybrids were raised by Gartner between Tropaeolum minus and majus (11/116.

'b.a.s.t.a.r.derzeugung' s. 549. It is, however, doubtful whether these plants should be ranked as species or varieties.) which at first produced flowers intermediate in size, colour, and structure between their two parents; but later in the season some of these plants produced flowers in all respects like those of the mother-form, mingled with flowers still retaining the usual intermediate condition. A hybrid Cereus between C. speciosissimus and phyllanthus (11/117. Gartner ibid s. 550.) plants which are widely different in appearance, produced for the first three years angular, five- sided stems, and then some flat stems like those of C. phyllanthus.

Kolreuter also gives cases of hybrid Lobelias and Verbasc.u.ms, which at first produced flowers of one colour, and later in the season, flowers of a different colour. (11/118. 'Journal de Physique' tome 23 1873 page 100.

'Act. Acad. St. Petersburgh' 1781 part 1 page 249.) Naudin (11/119.

'Nouvelles Archives du Museum' tome 1 page 49.) raised forty hybrids from Datura laevis fertilised by D. stramonium; and three of these hybrids produced many capsules, of which a half, or quarter, or lesser segment was smooth and of small size, like the capsule of the pure D. laevis, the remaining part being spinose and of larger size, like the capsule of the pure D. stramonium: from one of these composite capsules, plants perfectly resembling both parent-forms were raised.

Turning now to varieties. A SEEDLING apple, conjectured to be of crossed parentage, has been described in France (11/120. L'Hermes January 14, 1837 quoted in Loudon's 'Gardener's Mag.' volume 13 page 230.) which bears fruit with one half larger than the other, of a red colour, acid taste, and peculiar odour; the other side being greenish-yellow and very sweet: it is said scarcely ever to include perfectly developed seed. I suppose that this is not the same tree as that which Gaudichaud (11/121. 'Comptes Rendus'

tome 34 1852 page 746.) exhibited before the French inst.i.tute, bearing on the same branch two distinct kinds of apples, one a reinette rouge, and the other like a reinette canada jaunatre: this double-bearing variety can be propagated by grafts, and continues to produce both kinds; its origin is unknown. The Rev. J.D. La Touche sent me a coloured drawing of an apple which he brought from Canada, of which half, surrounding and including the whole of the calyx and the insertion of the foot-stalk, is green, the other half being brown and of the nature of the pomme gris apple, with the line of separation between the two halves exactly defined. The tree was a grafted one, and Mr. La Touche thinks that the branches which bore this curious apple sprung from the point of junction of the graft and stock: had this fact been ascertained, the case would probably have come into the cla.s.s of graft-hybrids already given. But the branch may have sprung from the stock, which no doubt was a seedling.

Prof. H. Lecoq, who has made a great number of crossings between the differently coloured varieties of Mirabilis jalapa (11/122. 'Geograph. Bot.

de l'Europe' tome 3 1854 page 405; and 'De la Fecondation' 1862 page 302.) finds that in the seedlings the colours rarely combine, but form distinct stripes; or half the flower is of one colour and half of a different colour. Some varieties regularly bear flowers striped with yellow, white, and red; but plants of such varieties occasionally produce on the same root branches with uniformly coloured flowers of all three tints, and other branches with half-and-half coloured flowers, and others with marbled flowers. Gallesio (11/123. 'Traite du Citrus' 1811 page 45.) crossed reciprocally white and red carnations, and the seedlings were striped; but some of the striped plants also bore entirely white and entirely red flowers. Some of these plants produced one year red flowers alone, and in the following year striped flowers; or conversely, some plants, after having borne for two or three years striped flowers, would revert and bear exclusively red flowers. It may be worth mentioning that I fertilised the PURPLE SWEET-PEA (Lathyrus odoratus) with pollen from the light-coloured PAINTED LADY: seedlings raised from the same pod were not intermediate in character, but perfectly resembled either parent. Later in the summer, the plants which had at first borne flowers identical with those of the PAINTED LADY, produced flowers streaked and blotched with purple; showing in these darker marks a tendency to reversion to the mother-variety. Andrew Knight (11/124. 'Transact. Linn. Soc.' volume 9 page 268.) fertilised two white grapes with pollen of the Aleppo grape, which is darkly variegated both in its leaves and fruit. The result was that the young seedlings were not at first variegated, but all became variegated during the succeeding summer; besides this, many produced on the same plant bunches of grapes which were all black, or all white, or lead-coloured striped with white, or white dotted with minute black stripes; and grapes of all these shades could frequently be found on the same foot-stalk.

I will append a very curious case, not of bud-variation, but of two cohering embryos, different in character and contained within the same seed. A distinguished botanist, Mr. G.H. Thwaites (11/125. 'Annals and Mag.

of Nat. Hist.' March 1848.) states that a seed from Fuchsia coccinea fertilised by F. fulgens, contained two embryos, and was "a true vegetable twin." The two plants produced from the two embryos were "extremely different in appearance and character," though both resembled other hybrids of the same parentage produced at the same time. These twin plants "were closely coherent, below the two pairs of cotyledon-leaves, into a single cylindrical stem, so that they had subsequently the appearance of being branches on one trunk." Had the two united stems grown up to their full height, instead of dying, a curiously mixed hybrid would have been produced. A mongrel melon described by Sageret (11/126. 'Pomologie Physiolog.' 1830 page 126.) may perhaps have thus originated; for the two main branches, which arose from two cotyledon-buds, produced very different fruit,--on the one branch like that of the paternal variety, and on the other branch like to a certain extent that of the maternal variety, the melon of China.]

In most of these cases of crossed varieties, and in some of the cases of crossed species, the colours proper to both parents appeared in the seedlings, as soon as they first flowered, in the form of stripes or larger segments, or as whole flowers or fruit of different kinds borne on the same plant; and in this case the appearance of the two colours cannot strictly be said to be due to reversion, but to some incapacity of fusion. When, however, the later flowers or fruit produced during the same season, or during a succeeding year or generation, become striped or half-and-half, etc., the segregation of the two colours is strictly a case of reversion by bud-variation. Whether all the many recorded cases of striped flowers and fruit are due to previous hybridisation and reversion is by no means clear, for instance with peaches and nectarines, moss-roses, etc. In a future chapter I shall show that, with animals of crossed parentage, the same individual has been known to change its character during growth, and to revert to one of its parents which it did not at first resemble. Finally, from the various facts now given, there can be no doubt that the same individual plant, whether a hybrid or a mongrel, sometimes returns in its leaves, flowers, and fruit, either wholly or by segments, to both parent- forms.

ON THE DIRECT OR IMMEDIATE ACTION OF THE MALE ELEMENT ON THE MOTHER FORM.

Another remarkable cla.s.s of facts must be here considered, firstly, because they have a high physiological importance, and secondly, because they have been supposed to account for some cases of bud-variation. I refer to the direct action of the male element, not in the ordinary way on the ovules, but on certain parts of the female plant, or in case of animals on the subsequent progeny of the female by a second male. I may premise that with plants the ovarium and the coats of the ovules are obviously parts of the female, and it could not have been antic.i.p.ated that they would have been affected by the pollen of a foreign variety or species, although the development of the embryo, inside the embryonic sack, inside the ovule and ovarium, of course, depends on the male element.

[Even as long ago as 1729 it was observed (11/127. 'Philosophical Transact.' volume 43 1744-45 page 525.) that white and blue varieties of the Pea, when planted near each other, mutually crossed, no doubt through the agency of bees, and in the autumn blue and white peas were found within the same pods. Wiegmann made an exactly similar observation in the present century. The same result has followed several times when a variety with peas of one colour has been artificially crossed by a differently-coloured variety. (11/128. Mr. Goss 'Transact. Hort. Soc.' volume 5 page 234: and Gartner 'b.a.s.t.a.r.derzeugung' 1849 ss. 81 and 499.) These statements led Gartner, who was highly sceptical on the subject, carefully to try a long series of experiments: he selected the most constant varieties, and the result conclusively showed that the colour of the skin of the pea is modified when pollen of a differently coloured variety is used. This conclusion has since been confirmed by experiments made by the Rev. J.M.

Berkeley. (11/129. 'Gardener's Chronicle' 1854 page 404.)

Mr. Laxton of Stamford, whilst making experiments on peas for the express purpose of ascertaining the influence of foreign pollen on the mother- plant, has recently (11/130. Ibid 1866 page 900.) observed an important additional fact. He fertilised the Tall Sugar-pea, which bears very thin green pods, becoming brownish-white when dry, with pollen of the Purple- podded pea, which, as its name expresses, has dark-purple pods with very thick skin, becoming pale reddish purple when dry. Mr. Laxton has cultivated the tall sugar-pea during twenty years, and has never seen or heard of it producing a purple pod: nevertheless, a flower fertilised by pollen from the purple-pod yielded a pod clouded with purplish-red which Mr. Laxton kindly gave to me. A s.p.a.ce of about two inches in length towards the extremity of the pod, and a smaller s.p.a.ce near the stalk, were thus coloured. On comparing the colour with that of the purple pod, both pods having been first dried and then soaked in water, it was found to be identically the same; and in both the colour was confined to the cells lying immediately beneath the outer skin of the pod. The valves of the crossed pod were also decidedly thicker and stronger than those of the pods of the mother-plant, but this may possibly have been an accidental circ.u.mstance, for I know not how far their thickness is a variable character in the Tall Sugar-pea.

The peas of the Tall Sugar-pea, when dry, are pale greenish-brown, thickly covered with dots of dark purple so minute as to be visible only through a lens, and Mr. Laxton has never seen or heard of this variety producing a purple pea; but in the crossed pod one of the peas was of a uniform beautiful violet-purple tint, and a second was irregularly clouded with pale purple. The colour lies in the outer of the two coats which surround the pea. As the peas of the purple-podded variety when dry are of a pale greenish-buff, it would at first appear that this remarkable change of colour in the peas in the crossed pod could not have been caused by the direct action of the pollen of the purple-pod: but when we bear in mind that this latter variety has purple flowers, purple marks on its stipules, and purple pods; and that the Tall Sugar-pea likewise has purple flowers and stipules, and microscopically minute purple dots on the peas, we can hardly doubt that the tendency to the production of purple in both parents has in combination modified the colour of the peas in the crossed pod.

After having examined these specimens, I crossed the same two varieties, and the peas in one pod but not the pods themselves, were clouded and tinted with purplish-red in a much more conspicuous manner than the peas in the uncrossed pods produced at the same time by the same plants. I may notice as a caution that Mr. Laxton sent me various other crossed peas slightly, or even greatly, modified in colour; but the change in these cases was due, as had been suspected by Mr. Laxton, to the altered colour of the cotyledons, seen through the transparent coats of the peas; and as the cotyledons are parts of the embryo, these cases are not in any way remarkable.

Turning now to the genus Matthiola. The pollen of one kind of stock sometimes affects the colour of the seeds of another kind, used as the mother-plant. I give the following case the more readily, as Gartner doubted similar statements previously made with respect to the stock by other observers. A well-known horticulturist, Major Trevor Clarke, informs me (11/131. See also a paper by this observer read before the International Hort. and Bot. Congress of London 1866.) that the seeds of the large red- flowered BIENNIAL stock, Matthiola annua (Cocardeau of the French), are light brown, and those of the purple branching Queen stock (M. incana) are violet-black; and he found that, when flowers of the red stock were fertilised by pollen from the purple stock, they yielded about fifty per cent of BLACK seeds. He sent me four pods from a red flowered plant, two of which had been fertilised by their own pollen, and they included pale brown seed; and two which had been crossed by pollen from the purple kind, and they included seeds all deeply tinged with black. These latter seeds yielded purple-flowered plants like their father; whilst the pale brown seeds yielded normal red-flowered plants; and Major Clarke, by sowing similar seeds, has observed on a greater scale the same result. The evidence in this case of the direct action of the pollen of one species on the colour of the seeds of another species appears to me conclusive.

Gallesio (11/132. 'Traite du Citrus' page 40.) fertilised the flowers of an orange with pollen from the lemon; and one fruit thus produced bore a longitudinal stripe of peel having the colour, flavour, and other characters of the lemon. Mr. Anderson (11/133. 'Transact. Hort. Soc.'

volume 3 page 318. See also volume 5 page 65.) fertilised a green-fleshed melon with pollen from a scarlet-fleshed kind; in two of the fruits "a sensible change was perceptible: and four other fruits were somewhat altered both internally and externally." The seeds of the two first- mentioned fruits produced plants partaking of the good properties of both parents. In the United States, where Cucurbitaceae are largely cultivated, it is the popular belief (11/134. Prof. Asa Gray 'Proc. Acad. Sc.' Boston volume 4 1860 page 21. I have received statements to the same effect from other persons in the United States.) that the fruit is thus directly affected hy foreign pollen; and I have received a similar statement with respect to the cuc.u.mber in England. It is believed that grapes have been thus affected in colour, size, and shape: in France a pale-coloured grape had its juice tinted by the pollen of the dark-coloured Teinturier; in Germany a variety bore berries which were affected by the pollen of two adjoining kinds; some of the berries being only partially affected or mottled. (11/135. For the French case see 'Journ. Hort. Soc.' volume 1 new series 1866 page 50. For Germany see M. Jack quoted in Henfrey's 'Botanical Gazette' volume 1 page 277. A case in England has recently been alluded to by the Rev. J.M. Berkeley before the Hort. Soc. of London.)

As long ago as 1751 (11/136. 'Philosophical Transactions' volume 47 1751-52 page 206.) it was observed that, when differently-coloured varieties of maize grew near each other, they mutually affected each other's seeds, and this is now a popular belief in the United States. Dr. Savi (11/137.

Gallesio 'Teoria della Riproduzione' 1816 page 95.) tried the experiment with care: he sowed yellow and black-seeded maize together, and on the same ear some of the seeds were yellow, some black, and some mottled, the differently coloured seeds being arranged irregularly or in rows. Prof.

Hildebrand has repeated the experiment (11/138. 'Bot. Zeitung' May 1868 page 326.) with the precaution of ascertaining that the mother-plant was true. A kind bearing yellow grains was fertilised with pollen of a kind having brown grains, and two ears produced yellow grains mingled with others of a dirty violet tint. A third ear had only yellow grains, but one side of the spindle was tinted of a reddish-brown; so that here we have the important fact of the influence of the foreign pollen extending to the axis. Mr. Arnold, in Canada, varied the experiment in an interesting manner: "a female flower was subjected first to the action of pollen from a yellow variety, and then to that from a white variety; the result was an ear, each grain of which was yellow below and white above." (11/139. See Dr. J. Stockton-Hough 'American Naturalist' January 1874 page 29.) With other plants it has occasionally been observed that the crossed offspring showed the influence of two kinds of pollen, but in this case the two kinds affected the mother-plant.

Mr. Sabine states (11/140. 'Transact. Hort. Soc.' volume 5 page 69.) that he has seen the form of the nearly globular seed-capsule of Amaryllis vittata altered by the application of the pollen of another species, of which the capsule has gibbous angles. With an allied genus, a well-known botanist, Maximowicz, has described in detail the striking results of reciprocally fertilising Lilium bulbiferum and davuric.u.m with each other's pollen. Each species produced fruit not like its own, but almost identical with that of the pollen-bearing species; but from an accident only the fruit of the latter species was carefully examined; the seeds were intermediate in the development of their wings. (11/141. 'Bull. de l'Acad.

Imp. de St. Petersburg' tome 17 page 275, 1872. The author gives references to those cases in the So1anaceae of fruit affected by foreign pollen, but as it does not appear that the mother-plant was artificially fertilised, I have not entered into details.)

Fritz Muller fertilised Cattleya leopoldi with pollen of Epidendron cinnabarinum; and the capsules contained very few seeds; but these presented a most wonderful appearance, which, from the description given, two botanists, Hildebrand and Maximowicz, attribute to the direct action of the pollen of the Epidendron. (11/142. 'Bot. Zeitung' September 1868 page 631. For Maximowicz's judgment see the paper last referred to.)

Mr. J. Anderson Henry (11/143. 'Journal of Horticulture' January 20, 1863 page 46.) crossed Rhododendron dalhousiae with the pollen of R. nuttallii, which is one of the largest-flowered and n.o.blest species of the genus. The largest pod produced by the former species, when fertilised with its own pollen, measured 1 2/8 inch in length and 1 1/2 in girth; whilst three of the pods which had been fertilised by pollen of R. nuttallii measured 1 5/8 inch in length and no less than 2 inches in girth. Here the effect of the foreign pollen was apparently confined to increasing the size of the ovarium; but we must be cautious in a.s.suming, as the following case shows, that size had been transferred from the male parent to the capsule of the female plant. Mr. Henry fertilised Arabis blepharophylla with pollen of A.

soyeri, and the pods thus produced, of which he was so kind as to send me detailed measurements and sketches, were much larger in all their dimensions than those naturally produced by either the male or female parent-species. In a future chapter we shall see that the organs of vegetation in hybrid plants, independently of the character of either parent, are sometimes developed to a monstrous size; and the increased size of the pods in the foregoing cases may be an a.n.a.logous fact. On the other hand, M. de Saporta informs me that an isolated female plant of Pistacia vera is very apt to be fertilised by the pollen of neighbouring plants of P. terebinthus, and in this case the fruits are only half their proper size, which he attributes to the influence of the pollen of P. terebinthus.

No case of the direct action of the pollen of one variety on another is better authenticated or more remarkable than that of the common apple. The fruit here consists of the lower part of the calyx and of the upper part of the flower-peduncle (11/144. See on this head the high authority of Prof.

Decaisne in a paper translated in 'Journ. Hort. Soc.' volume 1 new series 1866 page 48.) in a metamorphosed condition, so that the effect of the foreign pollen has extended even beyond the limits of the ovarium. Cases of apples thus affected were recorded by Bradley in the early part of the last century; and other cases are given in old volumes of the 'Philosophical Transactions' (11/145. Volume 43 1744-45 page 525 volume 45 1747-48 page 602.); in one of these a Russeting apple and an adjoining kind mutually affected each other's fruit; and in another case a smooth apple affected a rough-coated kind. Another instance has been given (11/146. 'Transact.

Hort. Soc.' volume 5 pages 65 and 68. See also Prof. Hildebrand with a coloured figure in 'Bot. Zeitung' May 15, 1868 page 327. Puvis also has collected 'De La Degeneration' 1837 page 36) several other instances; but it is not in all cases possible to distinguish between the direct action of foreign pollen and bud-variations.) of two very different apple-trees growing close to each other, which bore fruit resembling each other, but only on the adjoining branches. It is, however, almost superfluous to adduce these or other cases, after that of the St. Valery apple, the flowers which, from the abortion of the stamens, do not produce pollen, but are fertilised by the girls of the neighbourhood with pollen of many kinds; and they bear fruit, "differing from one another in size, flavour, and colour, but resembling in character the hermaphrodite kinds by which they have been fertilised." (11/147. T. de Clermont-Tonnerre in 'Mem. de la Soc.

Linn. de Paris' tome 3 1825 page 164.)]

I have now shown, on the authority of several excellent observers, in the case of plants belonging to widely different orders, that the pollen of one species or variety, when applied to the female of a distinct form, occasionally causes the coats of the seeds, the ovarium or fruit, including even the calyx and upper part of the peduncle of the apple, and the axis of the ear in maize, to be modified. Sometimes the whole ovarium or all the seeds are thus affected; sometimes only a certain number of the seeds, as in the case of the pea, or only a part of the ovarium, as with the striped orange, mottled grapes, and maize, is thus affected. It must not be supposed that any direct or immediate effect invariably follows the use of foreign pollen: this is far from being the case; nor is it known on what conditions the result depends. Mr. Knight (11/148. 'Transact. of Hort.

Soc.' volume 5 page 68.) expressly states that he has never seen the fruit thus affected, though he crossed thousands of apple and other fruit-trees.

There is not the least reason to believe that a branch which has borne seed or fruit directly modified by foreign pollen is itself affected, so as afterwards to produce modified buds; such an occurrence, from the temporary connection of the flower with the stem, would be hardly possible. Hence, but very few, if any, of the cases of bud-variation in the fruit of trees, given in the early part of this chapter can be accounted for by the action of foreign pollen; for such fruits have commonly been propagated by budding or grafting. It is also obvious that changes of colour in flowers, which necessarily supervene long before they are ready for fertilisation, and changes in the shape or colour of leaves, when due to the appearance of modified buds, can have no relation to the action of foreign pollen.

The proofs of the action of foreign pollen on the mother-plant have been given in considerable detail, because this action, as we shall see in a future chapter, is of the highest theoretical importance, and because it is in itself a remarkable and apparently anomalous circ.u.mstance. That it is remarkable under a physiological point of view is clear, for the male element not only affects, in accordance with its proper function, the germ, but at the same time various parts of the mother-plant, in the same manner, as it affects the same part in the seminal offspring from the same two parents. We thus learn that an ovule is not indispensable for the reception of the influence of the male element. But this direct action of the male element is not so anomalous as it at first appears, for it comes into play in the ordinary fertilisation of many flowers. Gartner gradually increased the number of pollen grains until he succeeded in fertilising a Malva, and has (11/149. Beitrage zur Kenntniss der Befruchtung' 1844 s. 347-351.) proved that many grains are first expended in the development, or, as he expresses it, in the satiation, of the pistil and ovarium. Again, when one plant is fertilised by a widely distinct species, it often happens that the ovarium is fully and quickly developed without any seeds being formed; or the coats of the seeds are formed without any embryo being developed within. Prof. Hildebrand, also, has lately shown (11/150. 'Die Fruchtbildung der Orchideen, ein Beweis fur die doppelte Wirkung des Pollens' 'Botanische Zeitung' No. 44 et seq. October 30, 1865; and August 4, 1865 s. 249.) that, in the normal fertilisation of several Orchideae, the action of the plant's own pollen is necessary for the development of the ovarium; and that this development takes place not only long before the pollen-tubes have reached the ovules, but even before the placentae and ovules have been formed; so that with these orchids the pollen acts directly on the ovarium. On the other hand, we must not overrate the efficacy of pollen in the case of hybridised plants, for an embryo may be formed and its influence excite the surrounding tissues of the mother- plant, and then perish at a very early age and be thus overlooked. Again, it is well known that with many plants the ovarium may be fully developed, though pollen be wholly excluded. Lastly, Mr. Smith, the late Curator at Kew (as I hear through Dr. Hooker), observed with an orchid, the Bonatea speciosa, the singular fact that the development of the ovarium could be effected by the mechanical irritation of the stigma. Nevertheless, from the number of the pollen-grains expended "in the satiation of the ovarium and pistil,"--from the generality of the formation of the ovarium and seed- coats in hybridised plants which produce no seeds,--and from Dr.

Hildebrand's observations on orchids, we may admit that in most cases the swelling of the ovarium, and the formation of the seed-coats are at least aided, if not wholly caused, by the direct action of the pollen, independently of the intervention of the fertilised germ. Therefore, in the previously given cases we have only to believe in the further power of pollen, when applied to a distinct species or variety, to influence the shape, size, colour, texture, etc., of certain parts of the mother-plant.

Turning now to the animal kingdom. If we could imagine the same flower to yield seeds during successive years, then it would not be very surprising that a flower of which the ovarium had been modified by foreign pollen should next year produce, when self-fertilised, offspring modified by the previous male influence. Closely a.n.a.logous cases have actually occurred with animals. In the case often quoted from Lord Morton (11/151. 'Philos.

Transact.' 1821 page 20.) a nearly purely-bred Arabian chestnut mare bore a hybrid to a quagga; she was subsequently sent to Sir Gore Ouseley, and produced two colts by a black Arabian horse. These colts were partially dun-coloured, and were striped on the legs more plainly than the real hybrid, or even than the quagga. One of the two colts had its neck and some other parts of its body plainly marked with stripes. Stripes on the body, not to mention those on the legs, are extremely rare,--I speak after having long attended to the subject,--with horses of all kinds in Europe, and are almost unknown in the case of Arabians. But what makes the case still more striking is that in these colts the hair of the mane resembled that of the quagga, being short, stiff, and upright. Hence there can be no doubt that the quagga affected the character of the offspring subsequently begot by the black Arabian horse. Mr. Jenner Weir informs me of a strictly parallel case: his neighbour Mr. Lethbridge, of Blackheath, has a horse, bred by Lord Mostyn, which had previously borne a foal by a quagga. This horse is dun with a dark stripe down the back, faint stripes on the forehead between the eyes, plain stripes on the inner side of the fore-legs and rather more faint ones on the hind-legs, with no shoulder-stripe. The mane grows much lower on the forehead than in the horse, but not so low as in the quagga or zebra. The hoofs are proportionally longer than in the horse,--so much so that the farrier who first shod this animal, and knew nothing of its origin, said, "Had I not seen I was shoeing a horse, I should have thought I was shoeing a donkey."

With respect to the varieties of our domesticated animals, many similar and well-authenticated facts have been published (11/152. Dr. Alex. Harvey on 'A remarkable Effect of Cross-breeding' 1851. On the 'Physiology of Breeding' by Mr. Reginald Orton 1855. 'Intermarriage' by Alex. Walker 1837.

'L'Heredite Naturelle' by Dr. Prosper Lucas tome 2 page 58. Mr. W. Sedgwick in 'British and Foreign Medico-Chirurgical Review' 1863 July page 183.

Bronn in his 'Geschichte der Natur' 1843 b. 2 s. 127 has collected several cases with respect to mares, sows, and dogs. Mr. W.C.L. Martin ('History of the Dog' 1845 page 104) says he can personally vouch for the influence of the male parent on subsequent litters by other dogs. A French poet, Jacques Savary, who wrote in 1665 on dogs, was aware of this singular fact. Dr.

Bowerbank has given us the following striking case:--A black, hairless Barbary b.i.t.c.h was first accidentally impregnated by a mongrel spaniel with long brown hair, and she produced five puppies, three of which were hairless and two covered with SHORT brown hair. The next time she was put to a black, hairless Barbary dog; "but the mischief had been implanted in the mother, and again about half the litter looked like pure Barbarys, and the other half like the SHORT-haired progeny of the first father." I have given in the text one case with pigs; an equally striking one has been recently published in Germany, 'Ill.u.s.t. Landwirth. Zeitung' 1868 November 17 page 143. It is worth notice that farmers in S. Brazil (as I hear from Fritz Muller), and at the C. of Good Hope (as I have heard from two trustworthy persons) are convinced that mares which have once borne mules, when subsequently put to horses, are extremely liable to produce colts, striped like a mule. Dr. Wilckens of Pogarth gives ('Jahrbuch Landwirthschaft' 2 1869 page 325) a striking and a.n.a.logous case. A merino ram, having two small lappets or flaps of skin on the neck, was in the winter of 1861-62 put to several Merino ewes, all of whom bore lambs with similar flaps on their necks. The ram was killed in the spring of 1862 and subsequently to his death the ewes were put to other Merino rams, and in 1863 to Southdown rams, none of whom ever have neck lappets: nevertheless, even as long afterwards as 1867, several of these ewes produced lambs bearing these appendages.), and others have been communicated to me, plainly showing the influence of the first male on the progeny subsequently borne by the mother to other males. It will suffice to give a single instance, recorded in the 'Philosophical Transactions,' in a paper following that by Lord Morton: Mr. Giles put a sow of Lord Western's black and white Ess.e.x breed to a wild boar of a deep chestnut colour; and the "pigs produced partook in appearance of both boar and sow, but in some the chestnut colour of the boar strongly prevailed." After the boar had long been dead, the sow was put to a boar of her own black and white breed--a kind which is well known to breed very true and never to show any chestnut colour,--yet from this union the sow produced some young pigs which were plainly marked with the same chestnut tint as in the first litter. Similar cases have so frequently occurred, that careful breeders avoid putting a choice female of any animal to an inferior male, on account of the injury to her subsequent progeny which may be expected to follow.

Some physiologists have attempted to account for these remarkable results from a previous impregnation, by the imagination of the mother having been strongly affected; but it will hereafter be seen that there are very slight grounds for any such belief. Other physiologists attribute the result to the close attachment and freely intercommunicating blood-vessels between the modified embryo and mother. But the a.n.a.logy from the action of foreign pollen on the ovarium, seed-coats, and other parts of the mother-plant, strongly supports the belief that with animals the male element acts directly on the female, and not through the crossed embryo. With birds there is no close connection between the embryo and mother; yet a careful observer, Dr. Chapuis, states (11/153. 'Le Pigeon Voyageur Belge' 1865 page 59.) that with pigeons the influence of a first male sometimes makes itself perceived in the succeeding broods; but this statement requires confirmation.

CONCLUSION AND SUMMARY OF THE CHAPTER.

The facts given in the latter half of this chapter are well worthy of consideration, as they show us in how many extraordinary modes the union of one form with another may lead to the modification of the seminal offspring or of the buds, afterwards produced.

There is nothing surprising in the offspring of species or varieties crossed in the ordinary manner being modified; but the case of two plants within the same seed, which cohere and differ from each other, is curious.

When a bud is formed after the cellular tissue of two species or two varieties have been united, and it partakes of the characters of both parents, the case is wonderful. But I need not here repeat what has been so lately said on this subject. We have also seen that in the case of plants the male element may affect in a direct manner the tissues of the mother, and with animals may lead to the modification of her future progeny. In the vegetable kingdom the offspring from a cross between two species or varieties, whether effected by seminal generation or by grafting, often revert, to a greater or less degree, in the first or in a succeeding generation, to the two parent-forms; and this reversion may affect the whole flower, fruit, or leaf-bud, or only the half or a smaller segment of a single organ. In some cases, however, such segregation of character apparently depends on an incapacity for union rather than on reversion, for the flowers or fruit which are first produced display by segments the characters of both parents. The various facts here given ought to be well considered by any one who wishes to embrace under a single point of view the many modes of reproduction by gemmation, division, and s.e.xual union, the reparation of lost parts, variation, inheritance, reversion, and other such phenomena. Towards the close of the second volume I shall attempt to connect these facts together by the hypothesis of pangenesis.

In the early half of the present chapter I have given a long list of plants in which through bud-variation, that is, independently of reproduction by seed, the fruit has suddenly become modified in size, colour, flavour, hairiness, shape, and time of maturity; flowers have similarly changed in shape, colour, in being double, and greatly in the character of the calyx; young branches or shoots have changed in colour, in bearing spines and in habit of growth, as in climbing or in weeping; leaves have changed in becoming variegated, in shape, period of unfolding, and in their arrangement on the axis. Buds of all kinds, whether produced on ordinary branches or on subterranean stems, whether simple or much modified and supplied with a stock of nutriment, as in tubers and bulbs, are all liable to sudden variations of the same general nature.

In the list, many of the cases are certainly due to reversion to characters not acquired from a cross, but which were formerly present and have since been lost for a longer or shorter time;--as when a bud on a variegated plant produces plain leaves, or when the variously-coloured flowers of the Chrysanthemum revert to the aboriginal yellow tint. Many other cases included in the list are probably due to the plants being of crossed parentage, and to the buds reverting either completely or by segments to one of the two parent-forms. (11/154. It may be worth while to call attention to the several means by which flowers and fruit become striped or mottled. Firstly, by the direct action of the pollen of another variety or species, as in the cases given of oranges and maize. Secondly, in crosses of the first generation, when the colours of the two parents do not readily unite, as with Mirabilis and Dianthus. Thirdly, in crossed plants of a subsequent generation by reversion, through either bud or seminal generation. Fourthly, by reversion to a character not originally gained by a cross, but which had long been lost, as with white-flowered varieties, which we shall hereafter see often become striped with some other colour.

Lastly, there are cases, as when peaches are produced with a half or quarter of the fruit like a nectarine, in which the change is apparently due to mere variation, through either bud or seminal generation.)

We may suspect that the strong tendency in the Chrysanthemum to produce by bud-variation differently-coloured flowers, results from the varieties having been at some time intentionally or accidentally crossed; and this is certainly the case with some kinds of Pelargonium. So it may be to a large extent with the bud-varieties of the Dahlia, and with the "broken colours "of Tulips. When, however, a plant reverts by bud-variation to its two parent forms, or to one of them, it sometimes does not revert perfectly, but a.s.sumes a somewhat new character,--of which fact, instances have been given, and Carriere gives (11/155. 'Production des Varietes' page 37.) another in the cherry.

Many cases of bud-variation, however, cannot be attributed to reversion, but to so-called spontaneous variability, as is so common with cultivated plants raised from seed. As a single variety of the Chrysanthemum has produced by buds six other varieties, and as one variety of the gooseberry has borne at the same time four distinct kinds of fruit, it is scarcely possible to believe that all these variations are due to reversion. We can hardly believe, as remarked in a previous chapter, that all the many peaches which have yielded nectarine-buds are of crossed parentage. Lastly, in such cases as that of the moss-rose, with its peculiar calyx, and of the rose which bears opposite leaves, in that of the Imatophyllum, etc., there is no known natural species or variety from which the characters in question could have been derived by a cross. We must attribute all such cases to the appearance of absolutely new characters in the buds. The varieties which have thus arisen cannot be distinguished by any external character from seedlings; this is notoriously the case with the varieties of the Rose, Azalea, and many other plants. It deserves notice that all the plants which have yielded bud-variations have likewise varied greatly by seed.

The plants which have varied by buds belong to so many orders that we may infer that almost every plant would be liable to variation, if placed under the proper exciting conditions. These conditions, as far as we can judge, mainly depend on long-continued and high cultivation; for almost all the plants in the foregoing list are perennials, and have been largely propagated in many soils, under different climates, by cuttings, offsets, bulbs, tubers, and especially by budding or grafting. The instances of annuals varying by buds, or producing on the same plant differently coloured flowers, are comparatively rare: Hopkirk (11/156. 'Flora Anomala'

page 164.) has seen this with Convolvulus tricolor; and it is not uncommon with the Balsam and annual Delphinium. According to Sir R. Schomburgk, plants from the warmer temperate regions, when cultivated under the hot climate of St. Domingo, are eminently liable to bud-variation. I am informed by Mr. Sedgwick that moss-roses which have often been taken to Calcutta always there lose their mossiness; but change of climate is by no means a necessary contingent, as we see with the gooseberry, currant, and in many other cases. Plants living under their natural conditions are very rarely subject to bud-variation. Variegated leaves have, however, been observed under such circ.u.mstances; and I have given an instance of variation by buds on an ash-tree planted in ornamental grounds, but it is doubtful whether such a tree can be considered as living under strictly natural conditions. Gartner has seen white and dark-red flowers produced from the same root of the wild Achillea millefolium; and Prof. Caspary has seen a completely wild Viola lutea bearing flowers of two different colours and sizes. (11/157. 'Schriften der physisch-okon. Gesell. zu Konigsberg' b.