done what is possible at present by a statistical investigation (17/30. ‘Journal of Statistical Soc.’ June 1875 page 153; and ‘Fortnightly Review’ June 1875.), and he has come to the conclusion, from his own researches and those of Dr. Mitchell, that the evidence as to any evil thus caused is conflicting, but on the whole points to the evil being very small.
BIRDS.
In the case of the FOWL a whole array of authorities could be given against too close interbreeding. Sir J. Sebright positively asserts that he made many trials, and that his fowls, when thus treated, became long in the legs, small in the body, and bad breeders. (17/31. ‘The Art of Improving the Breed’ page 13.) He produced the famous Sebright Bantams by complicated crosses, and by breeding in-and-in; and since his time there has been much close interbreeding with these animals; and they are now notoriously bad breeders. I have seen Silver Bantams, directly descended from his stock, which had become almost as barren as hybrids; for not a single chicken had been that year hatched from two full nests of eggs. Mr. Hewitt says that with these Bantams the sterility of the male stands, with rare exceptions, in the closest relation with their loss of certain secondary male characters: he adds, “I have noticed, as a general rule, that even the slightest deviation from feminine character in the tail of the male Sebright–say the elongation by only half an inch of the two principal tail feathers–brings with it improved probability of increased fertility.” (17/32. ‘The Poultry Book’ by W.B. Tegetmeier 1866 page 245.)
Mr. Wright states (17/33. ‘Journal Royal Agricult. Soc.’ 1846 volume 7 page 205; see also Ferguson on the Fowl pages 83, 317; see also ‘The Poultry Book’ by Tegetmeier 1866 page 135 with respect to the extent to which cock-fighters found that they could venture to breed in-and-in, viz., occasionally a hen with her own son; “but they were cautious not to repeat the in-and-in breeding.”) that Mr. Clark, “whose fighting-cocks were so notorious, continued to breed from his own kind till they lost their disposition to fight, but stood to be cut up without making any resistance, and were so reduced in size as to be under those weights required for the best prizes; but on obtaining a cross from Mr. Leighton, they again resumed their former courage and weight.” It should be borne in mind that game-cocks before they fought were always weighed, so that nothing was left to the imagination about any reduction or increase of weight. Mr. Clark does not seem to have bred from brothers and sisters, which is the most injurious kind of union; and he found, after repeated trials, that there was a greater reduction in weight in the young from a father paired with his daughter, than from a mother with her son. I may add that Mr. Eyton of Eyton, the well-known ornithologist, who is a large breeder of Grey Dorkings, informs me that they certainly diminish in size, and become less prolific, unless a cross with another strain is occasionally obtained. So it is with Malays, according to Mr. Hewitt, as far as size is concerned. (17/34. ‘The Poultry Book’ by W.B. Tegetmeier 1866 page 79.)
An experienced writer (17/35. ‘The Poultry Chronicle’ 1854 volume 1 page 43.) remarks that the same amateur, as is well known, seldom long maintains the superiority of his birds; and this, he adds, undoubtedly is due to all his stock “being of the same blood;” hence it is indispensable that he should occasionally procure a bird of another strain. But this is not necessary with those who keep a stock of fowls at different stations. Thus, Mr. Ballance, who has bred Malays for thirty years, and has won more prizes with these birds than any other fancier in England, says that breeding in-and-in does not necessarily cause deterioration; “but all depends upon how this is managed. My plan has been to keep about five or six distinct runs, and to rear about two hundred or three hundred chickens each year, and select the best birds from each run for crossing. I thus secure sufficient crossing to prevent deterioration.” (17/36. ‘The Poultry Book’ by W.B. Tegetmeier 1866 page 79.)
We thus see that there is almost complete unanimity with poultry-breeders that, when fowls are kept at the same place, evil quickly follows from interbreeding carried on to an extent which would be disregarded in the case of most quadrupeds. Moreover, it is a generally received opinion that cross- bred chickens are the hardiest and most easily reared. (17/37. ‘The Poultry Chronicle’ volume 1 page 89.) Mr. Tegetmeier, who has carefully attended to poultry of all breeds, says (17/38. ‘The Poultry Book’ 1866 page 210.) that Dorking hens, allowed to run with Houdan or Creve-coeur cocks, “produce in the early spring chickens that for size, hardihood, early maturity, and fitness for the market, surpass those of any pure breed that we have ever raised.” Mr. Hewitt gives it as a general rule with fowls, that crossing the breed increases their size. He makes this remark after stating that hybrids from the pheasant and fowl are considerably larger than either progenitor: so again, hybrids from the male golden pheasant and female common pheasant “are of far larger size than either parent-bird.” (17/39. Ibid 1866 page 167; and ‘Poultry Chronicle’ volume 3 1855 page 15.) To this subject of the increased size of hybrids I shall presently return.
With PIGEONS, breeders are unanimous, as previously stated, that it is absolutely indispensable, notwithstanding the trouble and expense thus caused, occasionally to cross their much-prized birds with individuals of another strain, but belonging, of course, to the same variety. It deserves notice that, when size is one of the desired characters, as with pouters (17/40. ‘A Treatise on Fancy Pigeons’ by J.M. Eaton page 56.) the evil effects of close interbreeding are much sooner perceived than when small birds, such as short- faced tumblers, are valued. The extreme delicacy of the high fancy breeds, such as these tumblers and improved English carriers, is remarkable; they are liable to many diseases, and often die in the egg or during the first moult; and their eggs have generally to be hatched under foster-mothers. Although these highly-prized birds have invariably been subjected to much close interbreeding, yet their extreme delicacy of constitution cannot perhaps be thus fully explained. Mr. Yarrell informed me that Sir J. Sebright continued closely interbreeding some owl-pigeons, until from their extreme sterility he as nearly as possible lost the whole family. Mr. Brent (17/41. ‘The Pigeon Book’ page 46.) tried to raise a breed of trumpeters, by crossing a common pigeon, and recrossing the daughter, granddaughter, great-granddaughter, and great-great-granddaughter, with the same male trumpeter, until he obtained a bird with 15/16 of trumpeter’s blood; but then the experiment failed, for “breeding so close stopped reproduction.” The experienced Neumeister (17/42. ‘Das Ganze der Taubenzucht’ 1837 s. 18.) also asserts that the offspring from dovecotes and various other breeds are “generally very fertile and hardy birds:” so again MM. Boitard and Corbie (17/43. ‘Les Pigeons’ 1824 page 35.), after forty-five years’ experience, recommend persons to cross their breeds for amusement; for, if they fail to make interesting birds, they will succeed under an economical point of view, “as it is found that mongrels are more fertile than pigeons of pure race.”
I will refer only to one other animal, namely, the Hive-bee, because a distinguished entomologist has advanced this as a case of inevitable close interbreeding. As the hive is tenanted by a single female, it might have been thought that her male and female offspring would always have bred together, more especially as bees of different hives are hostile to each other; a strange worker being almost always attacked when trying to enter another hive. But Mr. Tegetmeier has shown (17/44. ‘Proc. Entomolog. Soc.’ August 6, 1860 page 126.) that this instinct does not apply to drones, which are permitted to enter any hive; so that there is no a priori improbability of a queen receiving a foreign drone. The fact of the union invariably and necessarily taking place on the wing, during the queen’s nuptial flight, seems to be a special provision against continued interbreeding. However this may be, experience has shown, since the introduction of the yellow-banded Ligurian race into Germany and England, that bees freely cross: Mr. Woodbury, who introduced Ligurian bees into Devonshire, found during a single season that three stocks, at distances of from one to two miles from his hives, were crossed by his drones. In one case the Ligurian drones must have flown over the city of Exeter, and over several intermediate hives. On another occasion several common black queens were crossed by Ligurian drones at a distance of from one to three and a half miles. (17/45. ‘Journal of Horticulture’ 1861 pages 39, 77, 158; and 1864 page 206.)
PLANTS.
When a single plant of a new species is introduced into any country, if propagated by seed, many individuals will soon be raised, so that if the proper insects be present there will be crossing. With newly-introduced trees or other plants not propagated by seed we are not here concerned. With old- established plants it is an almost universal practice occasionally to make exchanges of seed, by which means individuals which have been exposed to different conditions of life,–and this, as we have seen with animals, diminishes the evil from close interbreeding,–will occasionally be introduced into each district.
With respect to individuals belonging to the same sub-variety, Gartner, whose accuracy and experience exceeded that of all other observers, states (17/46. ‘Beitrage zur Kenntniss der Befruchtung’ 1844 s. 366.) that he has many times observed good effects from this step, especially with exotic genera, of which the fertility is somewhat impaired, such as Passiflora, Lobelia, Fuchsia. Herbert also says (17/47. ‘Amaryllidaceae’ page 371.), “I am inclined to think that I have derived advantage from impregnating the flower from which I wished to obtain seed with pollen from another individual of the same variety, or at least from another flower, rather than with its own.” Again, Professor Lecoq ascertained that crossed offspring are more vigorous and robust than their parents. (17/48. ‘De la Fecondation’ 2nd edition 1862 page 79.)
General statements of this kind, however, can seldom be fully trusted: I therefore began a long series of experiments, continued for about ten years, which will I think conclusively show the good effects of crossing two distinct plants of the same variety, and the evil effects of long-continued self- fertilisation. A clear light will thus be thrown on such questions, as why flowers are almost invariably constructed so as to permit, or favour, or necessitate the union of two individuals. We shall clearly understand why monoecious and dioecious,–why dichogamous, dimorphic and trimorphic plants exist, and many other such cases. I intend soon to publish an account of these experiments, and I can here give only a few cases in illustration. The plan which I followed was to grow plants in the same pot, or in pots of the same size, or close together in the open ground; carefully to exclude insects; and then to fertilise some of the flowers with pollen from the same flower, and others on the same plant with pollen from a distinct but adjoining plant. In many of these experiments, the crossed plants yielded much more seed than the self-fertilised plants; and I have never seen the reversed case. The self- fertilised and crossed seeds thus obtained were allowed to germinate in the same glass vessel on damp sand; and as the seeds germinated, they were planted in pairs on opposite sides of the same pot, with a superficial partition between them, and were placed so as to be equally exposed to the light. In other cases the self-fertilised and crossed seeds were simply sown on opposite sides of the same small pot. I have, in short, followed different plans, but in every case have taken all the precautions which I could think of, so that the two lots should be equally favoured. The growth of the plants raised from the crossed and self-fertilised seed, were carefully observed from their germination to maturity, in species belonging to fifty-two genera; and the difference in their growth, and in withstanding unfavourable conditions, was in most cases manifest and strongly marked. It is of importance that the two lots of seed should be sown or planted on opposite sides of the same pot, so that the seedlings may struggle against each other; for if sown separately in ample and good soil, there is often but little difference in their growth.
I will briefly describe two of the first cases observed by me. Six crossed and six self-fertilised seeds of Ipomoea purpurea, from plants treated in the manner above described, were planted as soon as they had germinated, in pairs on opposite sides of two pots, and rods of equal thickness were given them to twine up. Five of the crossed plants grew from the first more quickly than the opposed self-fertilised plants; the sixth, however, was weakly and was for a time beaten, but at last its sounder constitution prevailed and it shot ahead of its antagonist. As soon as each crossed plant reached the top of its seven- foot rod its fellow was measured, and the result was that, when the crossed plants were seven feet high the self-fertilised had attained the average height of only five feet four and a half inches. The crossed plants flowered a little before, and more profusely than the self-fertilised plants. On opposite sides of another SMALL pot a large number of crossed and self-fertilised seeds were sown, so that they had to struggle for bare existence; a single rod was given to each lot: here again the crossed plants showed from the first their advantage; they never quite reached the summit of the seven-foot rod, but relatively to the self-fertilised plants their average height was as seven feet to five feet two inches. The experiment was repeated during several succeeding generations, treated in exactly the same manner, and with nearly the same result. In the second generation, the crossed plants, which were again crossed, produced 121 seed-capsules, whilst the self-fertilised, again self-fertilised, produced only 84 capsules.
Some flowers of the Mimulus luteus were fertilised with their own pollen, and others were crossed with pollen from distinct plants growing in the same pot. The seeds were thickly sown on opposite sides of a pot. The seedlings were at first equal in height; but when the young crossed plants were half an inch, the self-fertilised plants were only a quarter of an inch high. But this degree of inequality did not last, for, when the crossed plants were four and a half inches high, the self-fertilised were three inches, and they retained the same relative difference till their growth was complete. The crossed plants looked far more vigorous than the uncrossed, and flowered before them; they produced also a far greater number of capsules. As in the former case, the experiment was repeated during several succeeding generations. Had I not watched these plants of Mimulus and Ipomoea during their whole growth, I could not have believed it possible, that a difference apparently so slight as that of the pollen being taken from the same flower, or from a distinct plant growing in the same pot, could have made so wonderful a difference in the growth and vigour of the plants thus produced. This, under a physiological point of view, is a most remarkable phenomenon.
With respect to the benefit derived from crossing distinct varieties, plenty of evidence has been published. Sageret (17/49. ‘Memoire sur les Cucurbitacees’ pages 36, 28, 30.) repeatedly speaks in strong terms of the vigour of melons raised by crossing different varieties, and adds that they are more easily fertilised than common melons, and produce numerous good seed. Here follows the evidence of an English gardener (17/50. Loudon’s ‘Gardener’s Mag.’ volume 8 1832 page 52.): “I have this summer met with better success in my cultivation of melons, in an unprotected state, from the seeds of hybrids (i.e. mongrels) obtained by cross impregnation, than with old varieties. The offspring of three different hybridisations (one more especially, of which the parents were the two most dissimilar varieties I could select) each yielded more ample and finer produce than any one of between twenty and thirty established varieties.”
Andrew Knight (17/51. ‘Transact. Hort. Soc.’ volume 1 page 25.) believed that his seedlings from crossed varieties of the apple exhibited increased vigour and luxuriance; and M. Chevreul (17/52. ‘Annal. des Sc. Nat.’ 3rd series, Bot. tome 6 page 189.) alludes to the extreme vigour of some of the crossed fruit- trees raised by Sageret.
By crossing reciprocally the tallest and shortest peas, Knight (17/53. ‘Philosophical Transactions’ 1799 page 200.) says: “I had in this experiment a striking instance of the stimulative effects of crossing the breeds; for the smallest variety, whose height rarely exceeded two feet, was increased to six feet: whilst the height of the large and luxuriant kind was very little diminished.” Mr. Laxton gave me seed-peas produced from crosses between four distinct kinds; and the plants thus raised were extraordinarily vigorous, being in each case from one to two or three feet taller than the parent-forms growing close alongside them.
Wiegmann (17/54. ‘Ueber die Bastarderzeugung’ 1828 s. 32, 33. For Mr. Chaundy’s case see Loudon’s ‘Gardener’s Mag.’ volume 7 1831 page 696.) made many crosses between several varieties of cabbage; and he speaks with astonishment of the vigour and height of the mongrels, which excited the amazement of all the gardeners who beheld them. Mr. Chaundy raised a great number of mongrels by planting together six distinct varieties of cabbage. These mongrels displayed an infinite diversity of character; “But the most remarkable circumstance was, that, while all the other cabbages and borecoles in the nursery were destroyed by a severe winter, these hybrids were little injured, and supplied the kitchen when there was no other cabbage to be had.”
Mr. Maund exhibited before the Royal Agricultural Society (17/55. ‘Gardener’s Chronicle’ 1846 page 601.) specimens of crossed wheat, together with their parent varieties; and the editor states that they were intermediate in character, “united with that greater vigour of growth, which it appears, in the vegetable as in the animal world, is the result of a first cross.” Knight also crossed several varieties of wheat (17/56. ‘Philosoph. Transact.’ 1799 page 201.), and he says “that in the years 1795 and 1796, when almost the whole crop of corn in the island was blighted, the varieties thus obtained, and these only, escaped in this neighbourhood, though sown in several different soils and situations.”
Here is a remarkable case: M. Clotzsch (17/57. Quoted in ‘Bull. Bot. Soc. France’ volume 2 1855 page 327.) crossed Pinus sylvestris and nigricans, Quercus robur and pedunculata, Alnus glutinosa and incana, Ulmus campestris and effusa; and the cross-fertilised seeds, as well as seeds of the pure parent-trees, were all sown at the same time and in the same place. The result was, that after an interval of eight years, the hybrids were one-third taller than the pure trees!
The facts above given refer to undoubted varieties, excepting the trees crossed by Clotzsch, which are ranked by various botanists as strongly-marked races, sub-species, or species. That true hybrids raised from entirely distinct species, though they lose in fertility, often gain in size and constitutional vigour, is certain. It would be superfluous to quote any facts; for all experimenters, Kolreuter, Gartner, Herbert, Sageret, Lecoq, and Naudin, have been struck with the wonderful vigour, height, size, tenacity of life, precocity, and hardiness of their hybrid productions. Gartner (17/58. Gartner ‘Bastarderzeugung’ s. 259, 518, 526 et seq.) sums up his conviction on this head in the strongest terms. Kolreuter (17/59. ‘Fortsetzung’ 1763 s. 29; ‘Dritte Fortsetzung’ s. 44, 96; ‘Act. Acad. St. Petersburg’ 1782 part 2 page 251; ‘Nova Acta’ 1793 pages 391, 394; ‘Nova Acta’ 1795 pages 316, 323.) gives numerous precise measurements of the weight and height of his hybrids in his comparison with measurements of both parent-forms; and speaks with astonishment of their “statura portentosa,” their “ambitus vastissimus ac altitudo valde conspicua.” Some exceptions to the rule in the case of very sterile hybrids have, however, been noticed by Gartner and Herbert; but the most striking exceptions are given by Max Wichura (17/60. ‘Die Bastardbefruchtung’ etc. 1865 s. 31, 41, 42.) who found that hybrid willows were generally tender in constitution, dwarf, and short-lived.
Kolreuter explains the vast increase in the size of the roots, stems, etc., of his hybrids, as the result of a sort of compensation due to their sterility, in the same way as many emasculated animals are larger than the perfect males. This view seems at first sight extremely probable, and has been accepted by various authors (17/61. Max Wichura fully accepts this view (‘Bastardbefruchtung’ s. 43), as does the Rev. M.J. Berkeley in ‘Journal of Hort. Soc.’ January 1866 page 70.); but Gartner (17/62. ‘Bastarderzeugung’ s. 394, 526, 528.) has well remarked that there is much difficulty in fully admitting it; for with many hybrids there is no parallelism between the degree of their sterility and their increased size and vigour. The most striking instances of luxuriant growth have been observed with hybrids which were not sterile in any extreme degree. In the genus Mirabilis, certain hybrids are unusually fertile, and their extraordinary luxuriance of growth, together with their enormous roots (17/63. Kolreuter ‘Nova Acta’ 1795 page 316.) have been transmitted to their progeny. The result in all cases is probably in part due to the saving of nutriment and vital force through the sexual organs acting imperfectly or not at all, but more especially to the general law of good being derived from a cross. For it deserves especial attention that mongrel animals and plants, which are so far from being sterile that their fertility is often actually augmented, have, as previously shown, their size, hardiness, and constitutional vigour generally increased. It is not a little remarkable that an accession of vigour and size should thus arise under the opposite contingencies of increased and diminished fertility.
It is a perfectly well ascertained fact (17/64. Gartner ‘Bastarderzeugung’ s. 430.) that hybrids invariably breed with either pure parent, and not rarely with a distinct species, more readily than with one another. Herbert is inclined to explain even this fact by the advantage derived from a cross; but Gartner more justly accounts for it by the pollen of the hybrid, and probably its ovules, being in some degree vitiated, whereas the pollen and ovules of both pure parents and of any third species are sound. Nevertheless, there are some well-ascertained and remarkable facts, which, as we shall presently see, show that a cross by itself undoubtedly tends to increase or re-establish the fertility of hybrids.
The same law, namely, that the crossed offspring both of varieties and species are larger than the parent-forms, holds good in the most striking manner with hybrid animals as well as with mongrels. Mr. Bartlett, who has had such large experience says, “Among all hybrids of vertebrated animals there is a marked increase of size.” He then enumerates many cases with mammals, including monkeys, and with various families of birds. (17/65. Quoted by Dr. Murie in ‘Proc. Zoolog. Soc.’ 1870 page 40.)
ON CERTAIN HERMAPHRODITE PLANTS WHICH, EITHER NORMALLY OR ABNORMALLY, REQUIRE TO BE FERTILISED BY POLLEN FROM A DISTINCT INDIVIDUAL OR SPECIES.
The facts now to be given differ from the foregoing, as self-sterility is not here the result of long-continued close interbreeding. These facts are, however, connected with our present subject, because a cross with a distinct individual is shown to be either necessary or advantageous. Dimorphic and trimorphic plants, though they are hermaphrodites, must be reciprocally crossed, one set of forms by the other, in order to be fully fertile, and in some cases to be fertile in any degree. But I should not have noticed these plants, had it not been for the following cases given by Dr. Hildebrand (17/66. ‘Botanische Zeitung’ January 1864 s. 3.):–
Primula sinensis is a reciprocally dimorphic species: Dr. Hildebrand fertilised twenty-eight flowers of both forms, each by pollen of the other form, and obtained the full number of capsules containing on an average 42.7 seed per capsule; here we have complete and normal fertility. He then fertilised forty-two flowers of both forms with pollen of the same form, but taken from a distinct plant, and all produced capsules containing on an average only 19.6 seed. Lastly, and here we come to our more immediate point, he fertilised forty-eight flowers of both forms with pollen of the same form and taken from the same flower, and now he obtained only thirty-two capsules, and these contained on an average 18.6 seed, or one less per capsule than in the former case. So that, with these illegitimate unions, the act of impregnation is less assured, and the fertility slightly less, when the pollen and ovules belong to the same flower, than when belonging to two distinct individuals of the same form. Dr. Hildebrand has recently made analogous experiments on the long-styled form of Oxalis rosea, with the same result. (17/67. ‘Monatsbericht Akad. Wissen.’ Berlin 1866 s. 372.)
It has recently been discovered that certain plants, whilst growing in their native country under natural conditions, cannot be fertilised with pollen from the same plant. They are sometimes so utterly self-impotent, that, though they can readily be fertilised by the pollen of a distinct species or even distinct genus, yet, wonderful as is the fact, they never produce a single seed by their own pollen. In some cases, moreover, the plant’s own pollen and stigma mutually act on each other in a deleterious manner. Most of the facts to be given relate to orchids, but I will commence with a plant belonging to a widely different family.
Sixty-three flowers of Corydalis cava, borne on distinct plants, were fertilised by Dr. Hildebrand (17/68. International Hort. Congress, London 1866.) with pollen from other plants of the same species; and fifty-eight capsules were obtained, including on an average 4.5 seed in each. He then fertilised sixteen flowers produced by the same raceme, one with another, but obtained only three capsules, one of which alone contained any good seeds, namely, two in number. Lastly, he fertilised twenty-seven flowers, each with its own pollen; he left also fifty-seven flowers to be spontaneously fertilised, and this would certainly have ensued if it had been possible, for the anthers not only touch the stigma, but the pollen-tubes were seen by Dr. Hildebrand to penetrate it; nevertheless these eighty-four flowers did not produce a single seed-capsule! This whole case is highly instructive, as it shows how widely different the action of the same pollen is, according as it is placed on the stigma of the same flower, or on that of another flower on the same raceme, or on that of a distinct plant.
With exotic Orchids several analogous cases have been observed, chiefly by Mr. John Scott. (17/69. ‘Proc. Bot. Soc. of Edinburgh’ May 1863: these observations are given in abstract, and others are added, in the ‘Journal of Proc. of Linn. Soc.’ volume 8 Bot. 1864 page 162.) Oncidium sphacelatum has effective pollen, for Mr. Scott fertilised two distinct species with it; the ovules are likewise capable of impregnation, for they were readily fertilised by the pollen of O. divaricatum; nevertheless, between one and two hundred flowers fertilised by their own pollen did not produce a single capsule, though the stigmas were penetrated by the pollen-tubes. Mr. Robertson Munro, of the Royal Botanic Gardens of Edinburgh, also informs me (1864) that a hundred and twenty flowers of this same species were fertilised by him with their own pollen, and did not produce a capsule, but eight flowers, fertilised by the pollen of O. divaricatum, produced four fine capsules: again, between two and three hundred flowers of O. divaricatum, fertilised by their own pollen, did not set a capsule, but twelve flowers fertilised by O. flexuosum produced eight fine capsules: so that here we have three utterly self-impotent species, with their male and female organs perfect, as shown by their mutual fertilisation. In these cases fertilisation was effected only by the aid of a distinct species. But, as we shall presently see, distinct plants, raised from seed, of Oncidium flexuosum, and probably of the other species, would have been perfectly capable of fertilising each other, for this is the natural process. Again, Mr. Scott found that the pollen of a plant of O. microchilum was effective, for with it he fertilised two distinct species; he found its ovules good, for they could be fertilised by the pollen of one of these species, and by the pollen of a distinct plant of O. microchilum; but they could not be fertilised by pollen of the same plant, though the pollen-tubes penetrated the stigma. An analogous case has been recorded by M. Riviere (17/70. Prof. Lecoq ‘De la Fecondation’ 2nd edition 1862 page 76.) with two plants of O. cavendishianum, which were both self-sterile, but reciprocally fertilised each other. All these cases refer to the genus Oncidium, but Mr. Scott found that Maxillaria atro-rubens was “totally insusceptible of fertilisation with its own pollen,” but fertilised, and was fertilised by, a widely distinct species, viz. M. squalens.
As these orchids had been grown under unnatural conditions in hot-houses, I concluded that their self-sterility was due to this cause. But Fritz Muller informs me that at Desterro, in Brazil, he fertilised above one hundred flowers of the above-mentioned Oncidium flexuosum, which is there endemic, with its own pollen, and with that taken from distinct plants: all the former were sterile, whilst those fertilised by pollen from any OTHER PLANT of the same species were fertile. During the first three days there was no difference in the action of the two kinds of pollen: that placed on stigma of the same plant separated in the usual manner into grains, and emitted tubes which penetrated the column, and the stigmatic chamber shut itself; but only those flowers which had been fertilised by pollen taken from a distinct plant produced seed-capsules. On a subsequent occasion these experiments were repeated on a large scale with the same result. Fritz Muller found that four other endemic species of Oncidium were in like manner utterly sterile with their own pollen, but fertile with that from any other plant: some of them likewise produced seed-capsules when impregnated with pollen of widely distinct genera, such as Cyrtopodium, and Rodriguezia. Oncidium crispum, however, differs from the foregoing species in varying much in its self- sterility; some plants producing fine pods with their own pollen, others failing to do so in two or three instances, Fritz Muller observed that the pods produced by pollen taken from a distinct flower on the same plant, were larger than those produced by the flower’s own pollen. In Epidendrum cinnabarinum, an orchid belonging to another division of the family, fine pods were produced by the plant’s own pollen, but they contained by weight only about half as much seed as the capsules which had been fertilised by pollen from a distinct plant, and in one instance from a distinct species; moreover, a very large proportion, and in some cases nearly all the seeds produced by the plant’s own pollen, were destitute of an embryo. Some self-fertilised capsules of a Maxillaria were in a similar state.
Another observation made by Fritz Muller is highly remarkable, namely, that with various orchids the plant’s own pollen not only fails to impregnate the flower, but acts on the stigma, and is acted on, in an injurious or poisonous manner. This is shown by the surface of the stigma in contact with the pollen, and by the pollen itself becoming in from three to five days dark brown, and then decaying. The discoloration and decay are not caused by parasitic cryptograms, which were observed by Fritz Muller in only a single instance. These changes are well shown by placing on the same stigma, at the same time, the plant’s own pollen and that from a distinct plant of the same species, or of another species, or even of another and widely remote genus. Thus, on the stigma of Oncidium flexuosum, the plant’s own pollen and that from a distinct plant were placed side by side, and in five days’ time the latter was perfectly fresh, whilst the plant’s own pollen was brown. On the other hand, when the pollen of a distinct plant of the Oncidium flexuosum and of the Epidendrum zebra (nov. spec.?) were placed together on the same stigma, they behaved in exactly the same manner, the grains separating, emitting tubes, and penetrating the stigma, so that the two pollen-masses, after an interval of eleven days, could not be distinguished except by the difference of their caudicles, which, of course, undergo no change. Fritz Muller has, moreover, made a large number of crosses between orchids belonging to distinct species and genera, and he finds that in all cases when the flowers are not fertilised their footstalks first begin to wither; and the withering slowly spreads upwards until the germens fall off, after an interval of one or two weeks, and in one instance of between six and seven weeks; but even in this latter case, and in most other cases, the pollen and stigma remained in appearance fresh. Occasionally, however, the pollen becomes brownish, generally on the external surface, and not in contact with the stigma, as is invariably the case when the plant’s own pollen is applied.
Fritz Muller observed the poisonous action of the plant’s own pollen in the above-mentioned Oncidium flexuosum, O. unicorne, pubes (?), and in two other unnamed species. Also in two species of Rodriguezia, in two of Notylia, in one of Burlingtonia, and of a fourth genus in the same group. In all these cases, except the last, it was proved that the flowers were, as might have been expected, fertile with pollen from a distinct plant of the same species. Numerous flowers of one species of Notylia were fertilised with pollen from the same raceme; in two days’ time they all withered, the germens began to shrink, the pollen-masses became dark brown, and not one pollen-grain emitted a tube. So that in this orchid the injurious action of the plant’s own pollen is more rapid than with Oncidium flexuosum. Eight other flowers on the same raceme were fertilised with pollen from a distinct plant of the same species: two of these were dissected, and their stigmas were found to be penetrated by numberless pollen-tubes; and the germens of the other six flowers became well developed. On a subsequent occasion many other flowers were fertilised with their own pollen, and all fell off dead in a few days; whilst some flowers on the same raceme which had been left simply unfertilised adhered and long remained fresh. We have seen that in cross-unions between extremely distinct orchids the pollen long remains undecayed; but Notylia behaved in this respect differently; for when its pollen was placed on the stigma of Oncidium flexuosum, both the stigma and pollen quickly became dark brown, in the same manner as if the plant’s own pollen had been applied.
Fritz Muller suggests that, as in all these cases the plant’s own pollen is not only impotent (thus effectually preventing self-fertilisation), but likewise prevents, as was ascertained in the case of the Notylia and Oncidium flexuosum, the action of subsequently applied pollen from a distinct individual, it would be an advantage to the plant to have its own pollen rendered more and more deleterious; for the germens would thus quickly be killed, and dropping off, there would be no further waste in nourishing a part which ultimately could be of no avail.
The same naturalist found in Brazil three plants of a Bignonia growing near together. He fertilised twenty-nine flowerets on one of them with their own pollen, and they did not set a single capsule. Thirty flowers were then fertilised with pollen from a distinct plant, one of the three, and they yielded only two capsules. Lastly, five flowers were fertilised with pollen from a fourth plant growing at a distance, and all five produced capsules. Fritz Muller thinks that the three plants which grew near one another were probably seedlings from the same parent, and that from being closely related, they acted very feebly on one another. This view is extremely probable, for he has since shown in a remarkable paper (17/71. ‘Jenaische Zeitschrift fur Naturwiss.’ b. 7 page 22 1872 and page 441 1873. A large part of this paper has been translated in the ‘American Naturalist’ 1874 page 223.), that in the case of some Brazilian species of Abutilon, which are self-sterile, and between which he raised some complex hybrids, that these, if near relatives, were much less fertile inter se, than when not closely related.
We now come to cases closely analogous with those just given, but different in so far that only certain individuals of the species are self-sterile. This self-impotence does not depend on the pollen or ovules being in an unfit state for fertilisation, for both have been found effective in union with other plants of the same or of a distinct species. The fact of plants having acquired so peculiar a constitution, that they can be fertilised more readily by the pollen of a distinct species than by their own, is exactly the reverse of what occurs with all ordinary species. For in the latter the two sexual elements of the same individual plant are of course capable of freely acting on each other; but are so constituted that they are more or less impotent when brought into union with the sexual elements of a distinct species, and produce more or less sterile hybrids.
Gartner experimented on two plants of Lobelia fulgens, brought from separate places, and found (17/72. ‘Bastarderzeugung’ s. 64, 357.) that their pollen was good, for he fertilised with it L. cardinalis and syphilitica; their ovules were likewise good, for they were fertilised by the pollen of these same two species; but these two plants of L. fulgens could not be fertilised by their own pollen, as can generally be effected with perfect ease with this species. Again, the pollen of a plant of Verbascum nigrum grown in a pot was found by Gartner (17/73. Ibid s. 357.) capable of fertilising V. lychnitis and V. austriacum; the ovules could be fertilised by the pollen of V. thapsus; but the flowers could not be fertilised by their own pollen. Kolreuter, also (17/74. ‘Zweite Fortsetzung’ s. 10; ‘Dritte Forts.’ s. 40. Mr. Scott likewise fertilised fifty-four flowers of Verbascum phoeniceum, including two varieties, with their own pollen, and not a single capsule was produced. Many of the pollen-grains emitted their tubes, but only a few of them penetrated the stigmas; some slight effect however was produced, as many of the ovaries became somewhat developed: ‘Journal Asiatic Soc. Bengal’ 1867 page 150.), gives the case of three garden plants of Verbascum phoeniceum, which bore during two years many flowers; these he fertilised successfully with the pollen of no less than four distinct species, but they produced not a seed with their own apparently good pollen; subsequently these same plants, and others raised from seed, assumed a strangely fluctuating condition, being temporarily sterile on the male or female side, or on both sides, and sometimes fertile on both sides; but two of the plants were perfectly fertile throughout the summer.
With Reseda odorata I have found certain individuals quite sterile with their own pollen, and so it is with the indigenous Reseda lutea. The self-sterile plants of both species were perfectly fertile when crossed with pollen from any other individual of the same species. These observations will hereafter be published in another work, in which I shall also show that seeds sent to me by Fritz Muller produced by plants of Eschscholtzia californica which were quite self-sterile in Brazil, yielded in this country plants which were only slightly self-sterile.
It appears (17/75. Duvernoy quoted by Gartner ‘Bastarderzeugung’ s. 334) that certain flowers on certain plants of Lilium candidum can be fertilised more freely by pollen from a distinct individual than by their own. So, again, with the varieties of the potato. Tinzmann (17/76. ‘Gardener’s Chronicle’ 1846 page 183.), who made many trials with this plant, says that pollen from another variety sometimes “exerts a powerful influence, and I have found sorts of potatoes which would not bear seed from impregnation with the pollen of their own flowers would bear it when impregnated with other pollen.” It does not, however, appear to have been proved that the pollen which failed to act on the flower’s own stigma was in itself good.
In the genus Passiflora it has long been known that several species do not produce fruit, unless fertilised by pollen taken from distinct species: thus, Mr. Mowbray (17/77. ‘Transact. Hort. Soc.’ volume 7 1830 page 95.) found that he could not get fruit from P. alata and racemosa except by reciprocally fertilising them with each other’s pollen; and similar facts have been observed in Germany and France. (17/78. Prof. Lecoq ‘De la Fecondation’ 1845 page 70; Gartner ‘Bastarderzeugung’ s. 64.) I have received two accounts of P. quadrangularis never producing fruit from its own pollen, but doing so freely when fertilised in one case with the pollen of P. coerulea, and in another case with that of P. edulis. But in three other cases this species fruited freely when fertilised with its own pollen; and the writer in one case attributed the favourable result to the temperature of the house having been raised from 5 deg to 10 deg Fahr. above the former temperature, after the flowers were fertilised. (17/79. ‘Gardener’s Chronicle’ 1868 page 1341.) With respect to P. laurifolia, a cultivator of much experience has recently remarked (17/80. ‘Gardener’s Chronicle’ 1866 page 1068.) that the flowers “must be fertilised with the pollen of P. coerulea, or of some other common kind, as their own pollen will not fertilise them.” But the fullest details on this subject have been given by Messrs. Scott and Robertson Munro (17/81. ‘Journal of Proc. of Linn. Soc.’ volume 8 1864 page 1168. Mr. Robertson Munro in ‘Trans. Bot. Soc.’ of Edinburgh volume 9 page 399.): plants of Passiflora racemosa, coerulea, and alata flowered profusely during many years in the Botanic Gardens of Edinburgh, and, though repeatedly fertilised with their own pollen, never produced any seed; yet this occurred at once with all three species when they were crossed together in various ways. In the case of P. coerulea three plants, two of which grew in the Botanic Gardens, were all rendered fertile, merely by impregnating each with pollen of one of the others. The same result was attained in the same manner with P. alata, but with only one plant out of three. As so many self-sterile species of Passiflora have been mentioned, it should be stated that the flowers of the annual P. gracilis are nearly as fertile with their own pollen as with that from a distinct plant; thus sixteen flowers spontaneously self-fertilised produced fruit, each containing on an average 21.3 seed, whilst fruit from fourteen crossed flowers contained 24.1 seed.
Returning to P. alata, I have received (1866) some interesting details from Mr. Robertson Munro. Three plants, including one in England, have already been mentioned which were inveterately self-sterile, and Mr. Munro informs me of several others which, after repeated trials during many years, have been found in the same predicament. At some other places, however, this species fruits readily when fertilised with its own pollen. At Taymouth Castle there is a plant which was formerly grafted by Mr. Donaldson on a distinct species, name unknown, and ever since the operation it has produced fruit in abundance by its own pollen; so that this small and unnatural change in the state of this plant has restored its self-fertility! Some of the seedlings from the Taymouth Castle plant were found to be not only sterile with their own pollen, but with each other’s pollen, and with the pollen of distinct species. Pollen from the Taymouth plant failed to fertilise certain plants of the same species, but was successful on one plant in the Edinburgh Botanic Gardens. Seedlings were raised from this latter union, and some of their flowers were fertilised by Mr. Munro with their own pollen; but they were found to be as self-impotent as the mother-plant had always proved, except when fertilised by the grafted Taymouth plant, and except, as we shall see, when fertilised by her own seedlings. For Mr. Munro fertilised eighteen flowers on the self-impotent mother-plant with pollen from these her own self-impotent seedlings, and obtained, remarkable as the fact is, eighteen fine capsules full of excellent seed! I have met with no case in regard to plants which shows so well as this of P. alata, on what small and mysterious causes complete fertility or complete sterility depends.
The facts hitherto given relate to the much-lessened or completely destroyed fertility of pure species when impregnated with their own pollen, in comparison with their fertility when impregnated by distinct individuals or distinct species; but closely analogous facts have been observed with hybrids.
Herbert states (17/82. ‘Amaryllidaceae’ 1837 page 371; ‘Journal of Hort. Soc.’ volume 2 1847 page 19.) that having in flower at the same time nine hybrid Hippeastrums, of complicated origin, descended from several species, he found that “almost every flower touched with pollen from another cross produced seed abundantly, and those which were touched with their own pollen either failed entirely, or formed slowly a pod of inferior size, with fewer seeds.” In the ‘Horticultural Journal’ he adds that “the admission of the pollen of another cross-bred Hippeastrum (however complicated the cross) to any one flower of the number, is almost sure to check the fructification of the others.” In a letter written to me in 1839, Dr. Herbert says that he had already tried these experiments during five consecutive years, and he subsequently repeated them, with the same invariable result. He was thus led to make an analogous trial on a pure species, namely, on the Hippeastrum aulicum, which he had lately imported from Brazil: this bulb produced four flowers, three of which were fertilised by their own pollen, and the fourth by the pollen of a triple cross between H. bulbulosum, reginae, and vittatum; the result was, that “the ovaries of the three first flowers soon ceased to grow, and after a few days perished entirely: whereas the pod impregnated by the hybrid made vigorous and rapid progress to maturity, and bore good seed, which vegetated freely.” This is, indeed, as Herbert remarks, “a strange truth,” but not so strange as it then appeared.
As a confirmation of these statements, I may add that Mr. M. Mayes (17/83. Loudon’s ‘Gardener’s Magazine’ volume 11 1835 page 260.) after much experience in crossing the species of Amaryllis (Hippeastrum), says, “neither the species nor the hybrids will, we are well aware, produce seed so abundantly from their own pollen as from that of others.” So, again, Mr. Bidwell, in New South Wales (17/84. ‘Gardener’s Chronicle’ 1850 page 470.) asserts that Amaryllis belladonna bears many more seeds when fertilised by the pollen of Brunswigia (Amaryllis of some authors) josephinae or of B. multiflora, than when fertilised by its own pollen. Mr. Beaton dusted four flowers of a Cyrtanthus with their own pollen, and four with the pollen of Vallota (Amaryllis) purpurea; on the seventh day “those which received their own pollen slackened their growth, and ultimately perished; those which were crossed with the Vallota held on.” (17/85. ‘Journal Hort. Soc.’ volume 5 page 135. The seedlings thus raised were given to the Hort. Soc.; but I find, on inquiry, that they unfortunately died the following winter.) These latter cases, however, relate to uncrossed species, like those before given with respect to Passiflora, Orchids, etc., and are here referred to only because the plants belong to the same group of Amaryllidaceae.
In the experiments on the hybrid Hippeastrums, if Herbert had found that the pollen of two or three kinds alone had been more efficient on certain kinds than their own pollen, it might have been argued that these, from their mixed parentage, had a closer mutual affinity than the others; but this explanation is inadmissible, for the trials were made reciprocally backwards and forwards on nine different hybrids; and a cross, whichever way taken, always proved highly beneficial. I can add a striking and analogous case from experiments made by the Rev. A. Rawson, of Bromley Common, with some complex hybrids of Gladiolus. This skilful horticulturist possessed a number of French varieties, differing from each other only in the colour and size of the flowers, all descended from Gandavensis, a well-known old hybrid, said to be descended from G. natalensis by the pollen of G. oppositiflorus. (17/86. Mr. D. Beaton in ‘Journal of Hort.’ 1861 page 453. Lecoq however (‘De la Fecond.’ 1862 page 369) states that this hybrid is descended from G. psittacinus and cardinalis; but this is opposed to Herbert’s experience, who found that the former species could not be crossed.) Mr. Rawson, after repeated trials, found that none of the varieties would set seed with their own pollen, although taken from distinct plants of the same variety (which had, of course, been propagated by bulbs), but that they all seeded freely with pollen from any other variety. To give two examples: Ophir did not produce a capsule with its own pollen, but when fertilised with that of Janire, Brenchleyensis, Vulcain and Linne, it produced ten fine capsules; but the pollen of Ophir was good, for when Linne was fertilised by it seven capsules were produced. This latter variety, on the other hand, was utterly barren with its own pollen, which we have seen was perfectly efficient on Ophir. Altogether, Mr. Rawson, in the year 1861 fertilised twenty-six flowers borne by four varieties with pollen taken from other varieties, and every single flower produced a fine seed-capsule; whereas fifty-two flowers on the same plants, fertilised at the same time with their own pollen, did not yield a single seed-capsule. Mr. Rawson fertilised, in some cases, the alternate flowers, and in other cases all those down one side of the spike, with pollen of other varieties, and the remaining flowers with their own pollen. I saw these plants when the capsules were nearly mature, and their curious arrangement at once brought full conviction to the mind that an immense advantage had been derived from crossing these hybrids.
Lastly, I have heard from Dr. E. Bornet, of Antibes, who has made numerous experiments in crossing the species of Cistus, but has not yet published the results, that, when any of these hybrids are fertile, they may be said to be, in regard to function, dioecious; “for the flowers are always sterile when the pistil is fertilised by pollen taken from the same flower or from flowers on the same plant. But they are often fertile if pollen be employed from a distinct individual of the same hybrid nature, or from a hybrid made by a reciprocal cross.”
CONCLUSION.
That plants should be self-sterile, although both sexual elements are in a fit state for reproduction, appears at first sight opposed to all analogy. With respect to the species, all the individuals of which are in this state, although living under their natural conditions, we may conclude that their self-sterility has been acquired for the sake of effectually preventing self- fertilisation. The case is closely analogous with that of dimorphic and trimorphic or heterostyled plants, which can be fully fertilised only by plants belonging to a different form, and not, as in the foregoing cases, indifferently by any other individual of the species. Some of these hetero- styled plants are completely sterile with pollen taken from the same plant or from the same form. With respect to species living under their natural conditions, of which only certain individuals are self-sterile (as with Reseda lutea), it is probable that these have been rendered self-sterile to ensure occasional cross-fertilisation, whilst other individuals have remained self- fertile to ensure the propagation of the species. The case seems to be parallel with that of plants which produce, as Hermann Muller has discovered, two forms–one bearing more conspicuous flowers with their structure adapted for cross-fertilisation by insects, and the other form with less conspicuous flowers adapted for self-fertilisation. The self-sterility, however, of some of the foregoing plants is incidental on the conditions to which they have been subjected, as with the Eschscholtzia, the Verbascum phoeniceum (the sterility of which varied according to the season), and with the Passiflora alata, which recovered its self-fertility when grafted on a different stock.
It is interesting to observe in the above several cases the graduated series from plants which, when fertilised by their own pollen, yield the full number of seeds, but with the seedlings a little dwarfed in stature–to plants which when self-fertilised yield few seeds–to those which yield none, but have their ovaria somewhat developed–and, lastly, to those in which the plant’s own pollen and stigma mutually act on one another like poison. It is also interesting to observe on how slight a difference in the nature of the pollen or of the ovules complete self-sterility or complete self-fertility must depend in some of the above cases. Every individual of the self-sterile species appears to be capable of producing the full complement of seed when fertilised by the pollen of any other individual (though judging from the facts given with respect to Abutilon the nearest kin must be excepted); but not one individual can be fertilised by its own pollen. As every organism differs in some slight degree from every other individual of the same species, so no doubt it is with their pollen and ovules; and in the above cases we must believe that complete self-sterility and complete self-fertility depend on such slight differences in the ovules and pollen, and not their having been differentiated in some special manner in relation to one another; for it is impossible that the sexual elements of many thousand individuals should have been specialised in relation to every other individual. In some, however, of the above cases, as with certain Passifloras, an amount of differentiation between the pollen and ovules sufficient for fertilisation is gained only by employing pollen from a distinct species; but this is probably the result of such plants having been rendered somewhat sterile from the unnatural conditions to which they have been exposed.
Exotic animals confined in menageries are sometimes in nearly the same state as the above-described self-impotent plants; for, as we shall see in the following chapter, certain monkeys, the larger carnivora, several finches, geese, and pheasants, cross together, quite as freely as, or even more freely than the individuals of the same species breed together. Cases will, also, be given of sexual incompatibility between certain, male and female domesticated animals, which, nevertheless, are fertile when matched with any other individual of the same kind.
In the early part of this chapter it was shown that the crossing of individuals belonging to distinct families of the same race, or to different races or species, gives increased size and constitutional vigour to the offspring, and, except in the case of crossed species, increased fertility. The evidence rests on the universal testimony of breeders (for it should be observed that I am not here speaking of the evil results of close interbreeding), and is practically exemplified in the higher value of cross- bred animals for immediate consumption. The good results of crossing have also been demonstrated with some animals and with numerous plants, by actual weight and measurement. Although animals of pure blood will obviously be deteriorated by crossing, as far as their characteristic qualities are concerned, there seems to be no exception to the rule that advantages of the kind just mentioned are thus gained, even when there has not been any previous close interbreeding; and the rule applies to such animals as cattle and sheep, which can long resist breeding in-and-in between the nearest blood-relations.
In the case of crossed species, although size, vigour, precocity, and hardiness are, with rare exceptions, gained, fertility, in a greater or less degree, is lost; but the gain in the above respects can hardly be attributed to the principle of compensation; for there is no close parallelism between the increased size and vigour of hybrid offspring and their sterility. Moreover, it has been clearly proved that mongrels which are perfectly fertile gain these same advantages as well as sterile hybrids.
With the higher animals no special adaptations for ensuring occasional crosses between distinct families seem to exist. The eagerness of the males, leading to severe competition between them, is sufficient; for even with gregarious animals, the old and dominant males will be dispossessed after a time and it would be a mere chance if a closely related member of the same family were to be the victorious successor. The structure of many of the lower animals, when they are hermaphrodites, is such as to prevent the ovules being fertilised by the male element of the same individual; so that the concourse of two individuals is necessary. In other cases the access of the male element of a distinct individual is at least possible. With plants, which are affixed to the ground and cannot wander from place to place like animals, the numerous adaptations for cross-fertilisation are wonderfully perfect, as has been admitted by every one who has studied the subject.
The evil consequences of long-continued close interbreeding are not so easily recognised as the good effects from crossing, for the deterioration is gradual. Nevertheless, it is the general opinion of those who have had most experience, especially with animals which propagate quickly, that evil does inevitably follow sooner or later, but at different rates with different animals. No doubt a false belief may, like a superstition, prevail widely; yet it is difficult to suppose that so many acute observers have all been deceived at the expense of much cost and trouble. A male animal may sometimes be paired with his daughter, granddaughter, and so on, even for seven generations, without any manifest bad result: but the experiment has never been tried of matching brothers and sisters, which is considered the closest form of interbreeding, for an equal number of generations. There is good reason to believe that by keeping the members of the same family in distinct bodies, especially if exposed to somewhat different conditions of life, and by occasionally crossing these families, the evil results of interbreeding may be much diminished or quite eliminated. These results are loss of constitutional vigour, size, and fertility; but there is no necessary deterioration in the general form of the body, or in other good qualities. We have seen that with pigs first-rate animals have been produced after long-continued close interbreeding, though they had become extremely infertile when paired with their near relations. The loss of fertility, when it occurs, seems never to be absolute, but only relative to animals of the same blood; so that this sterility is to a certain extent analogous with that of self-impotent plants which cannot be fertilised by their own pollen, but are perfectly fertile with pollen of any other individual of the same species. The fact of infertility of this peculiar nature being one of the results of long-continued interbreeding, shows that interbreeding does not act merely by combining and augmenting various morbid tendencies common to both parents; for animals with such tendencies, if not at the time actually ill, can generally propagate their kind. Although offspring descended from the nearest blood-relations are not necessarily deteriorated in structure, yet some authors believe that they are eminently liable to malformations; and this is not improbable, as everything which lessens the vital powers acts in this manner. Instances of this kind have been recorded in the case of pigs, bloodhounds, and some other animals.
Finally, when we consider the various facts now given which plainly show that good follows from crossing, and less plainly that evil follows from close interbreeding, and when we bear in mind that with very many organisms elaborate provisions have been made for the occasional union of distinct individuals, the existence of a great law of nature is almost proved; namely, that the crossing of animals and plants which are not closely related to each other is highly beneficial or even necessary, and that interbreeding prolonged during many generations is injurious.
CHAPTER 2. XVIII. ON THE ADVANTAGES AND DISADVANTAGES OF CHANGED CONDITIONS OF LIFE: STERILITY FROM VARIOUS CAUSES.
ON THE GOOD DERIVED FROM SLIGHT CHANGES IN THE CONDITIONS OF LIFE.
In considering whether any facts were known which might throw light on the conclusion arrived at in the last chapter, namely, that benefits ensue from crossing, and that it is a law of nature that all organic beings should occasionally cross, it appeared to me probable that the good derived from slight changes in the conditions of life, from being an analogous phenomenon, might serve this purpose. No two individuals, and still less no two varieties, are absolutely alike in constitution and structure; and when the germ of one is fertilised by the male element of another, we may believe that it is acted on in a somewhat similar manner as an individual when exposed to slightly changed conditions. Now, every one must have observed the remarkable influence on convalescents of a change of residence, and no medical man doubts the truth of this fact. Small farmers who hold but little land are convinced that their cattle derive great benefit from a change of pasture. In the case of plants, the evidence is strong that a great advantage is derived from exchanging seeds, tubers, bulbs, and cuttings from one soil or place to another as different as possible.
The belief that plants are thus benefited, whether or not well founded, has been firmly maintained from the time of Columella, who wrote shortly after the Christian era, to the present day; and it now prevails in England, France, and Germany. (18/1. For England see below. For Germany see Metzger ‘Getreidearten’ 1841 s. 63. For France Loiseleur-Deslongchamps (‘Consid. sur les Cereales’ 1843 page 200) gives numerous references on this subject. For Southern France see Godron ‘Florula Juvenalis’ 1854 page 28.) A sagacious observer, Bradley, writing in 1724 (18/2. ‘A General Treatise of Husbandry’ volume 3 page 58.), says, “When we once become Masters of a good Sort of Seed, we should at least put it into Two or Three Hands, where the Soils and Situations are as different as possible; and every Year the Parties should change with one another; by which Means, I find the Goodness of the Seed will be maintained for several Years. For Want of this Use many Farmers have failed in their Crops and been great Losers.” He then gives his own practical experience on this head. A modern writer (18/3. ‘Gardener’s Chronicle and Agricult. Gazette’ 1858 page 247; and for the second statement, Ibid 1850 page 702. On this same subject see also Rev. D. Walker ‘Prize Essay of Highland Agricult. Soc.’ volume 2 page 200. Also Marshall ‘Minutes of Agriculture’ November 1775.) asserts, “Nothing can be more clearly established in agriculture than that the continual growth of any one variety in the same district makes it liable to deterioration either in quality or quantity.” Another writer states that he sowed close together in the same field two lots of wheat-seed, the product of the same original stock, one of which had been grown on the same land and the other at a distance, and the difference in favour of the crop from the latter seed was remarkable. A gentleman in Surrey who has long made it his business to raise wheat to sell for seed, and who has constantly realised in the market higher prices than others, assures me that he finds it indispensable continually to change his seed; and that for this purpose he keeps two farms differing much in soil and elevation.
With respect to the tubers of the potato, I find that at the present day the practice of exchanging sets is almost everywhere followed. The great growers of potatoes in Lancashire formerly used to get tubers from Scotland, but they found that “a change from the moss-lands, and vice versa, was generally sufficient.” In former times in France the crop of potatoes in the Vosges had become reduced in the course of fifty or sixty years in the proportion from 120-150 to 30-40 bushels; and the famous Oberlin attributed the surprising good which he effected in large part to changing the sets. (18/4. Oberlin ‘Memoirs’ English translation page 73. For Lancashire see Marshall ‘Review of Reports’ 1808 page 295.)
A well-known practical gardener, Mr. Robson (18/5. ‘Cottage Gardener’ 1856 page 186. For Mr. Robson’s subsequent statements see ‘Journal of Horticulture’ February 18, 1866 page 121. For Mr. Abbey’s remarks on grafting etc. Ibid July 18, 1865 page 44.) positively states that he has himself witnessed decided advantage from obtaining bulbs of the onion, tubers of the potato, and various seeds, all of the same kind, from different soils and distant parts of England. He further states that with plants propagated by cuttings, as with the Pelargonium, and especially the Dahlia, manifest advantage is derived from getting plants of the same variety, which have been cultivated in another place; or, “where the extent of the place allows, to take cuttings from one description of soil to plant on another, so as to afford the change that seems so necessary to the well-being of the plants.” He maintains that after a time an exchange of this nature is “forced on the grower, whether he be prepared for it or not.” Similar remarks have been made by another excellent gardener, Mr. Fish, namely, that cuttings of the same variety of Calceolaria, which he obtained from a neighbour, “showed much greater vigour than some of his own that were “treated in exactly the same manner,” and he attributed this solely to his own plants having become “to a certain extent worn out or tired of their quarters.” Something of this kind apparently occurs in grafting and budding fruit-trees; for, according to Mr. Abbey, grafts or buds generally take with greater facility on a distinct variety or even species, or on a stock previously grafted, than on stocks raised from seeds of the variety which is to be grafted; and he believes this cannot be altogether explained by the stocks in question being better adapted to the soil and climate of the place. It should, however, be added, that varieties grafted or budded on very distinct kinds, though they may take more readily and grow at first more vigorously than when grafted on closely allied stocks, afterwards often become unhealthy.
I have studied M. Tessier’s careful and elaborate experiments (18/6. ‘Mem. de l’Acad. des Sciences’ 1790 page 209.) made to disprove the common belief that good is derived from a change of seed; and he certainly shows that the same seed may with care be cultivated on the same farm (it is not stated whether on exactly the same soil) for ten consecutive years without loss. Another excellent observer, Colonel Le Couteur (18/7. ‘On the Varieties of Wheat’ page 52.) has come to the same conclusion; but then he expressly adds, if the same seed be used, “that which is grown on land manured from the mixen one year becomes seed for land prepared with lime, and that again becomes seed for land dressed with ashes, then for land dressed with mixed manure, and so on.” But this in effect is a systematic exchange of seed, within the limits of the same farm.
On the whole the belief, which has long been held by many cultivators, that good follows from exchanging seed, tubers, etc., seems to be fairly well founded. It seems hardly credible that the advantage thus derived can be due to the seeds, especially if very small ones, obtaining in one soil some chemical element deficient in the other and in sufficient quantity to influence the whole after-growth of the plant. As plants after once germinating are fixed to the same spot, it might have been anticipated that they would show the good effects of a change more plainly than do animals which continually wander about; and this apparently is the case. Life depending on, or consisting in, an incessant play of the most complex forces, it would appear that their action is in some way stimulated by slight changes in the circumstances to which each organism is exposed. All forces throughout nature, as Mr. Herbert Spencer (18/8. Mr. Spencer has fully and ably discussed this whole subject in his ‘Principles of Biology’ 1864 volume 2 chapter 10. In the first edition of my ‘Origin of Species’ 1859 page 267, I spoke of the good effects from slight changes in the conditions of life and from cross-breeding, and of the evil effects from great changes in the conditions and from crossing widely distinct forms, as a series of facts “connected together by some common but unknown bond, which is essentially related to the principle of life.) remarks, tend towards an equilibrium, and for the life of each organism it is necessary that this tendency should be checked. These views and the foregoing facts probably throw light, on the one hand, on the good effects of crossing the breed, for the germ will be thus slightly modified or acted on by new forces; and on the other hand, on the evil effects of close interbreeding prolonged during many generations, during which the germ will be acted on by a male having almost identically the same constitution.
STERILITY FROM CHANGED CONDITIONS OF LIFE.
I will now attempt to show that animals and plants, when removed from their natural conditions, are often rendered in some degree infertile or completely barren; and this occurs even when the conditions have not been greatly changed. This conclusion is not necessarily opposed to that at which we have just arrived, namely, that lesser changes of other kinds are advantageous to organic beings. Our present subject is of some importance, from having an intimate connection with the causes of variability. Indirectly it perhaps bears on the sterility of species when crossed: for as, on the one hand, slight changes in the conditions of life are favourable to plants and animals, and the crossing of varieties adds to the size, vigour, and fertility of their offspring; so, on the other hand, certain other changes in the conditions of life cause sterility; and as this likewise ensues from crossing much-modified forms or species, we have a parallel and double series of facts, which apparently stand in close relation to each other.
It is notorious that many animals, though perfectly tamed, refuse to breed in captivity. Isidore Geoffroy St.-Hilaire (18/9. ‘Essais de Zoologie Generale’ 1841 page 256. ) consequently has drawn a broad distinction between tamed animals which will not breed under captivity, and truly domesticated animals which breed freely–generally more freely, as shown in the sixteenth chapter, than in a state of nature. It is possible and generally easy to tame most animals; but experience has shown that it is difficult to get them to breed regularly, or even at all. I shall discuss this subject in detail; but will give only those cases which seem most illustrative. My materials are derived from notices scattered through various works, and especially from a Report, kindly drawn up for me by the officers of the Zoological Society of London, which has especial value, as it records all the cases, during nine years from 1838-46, in which the animals were seen to couple but produced no offspring, as well as the cases in which they never, as far as known, coupled. This MS. Report I have corrected by the annual Reports subsequently published up to the year 1865. (18/10. Since the appearance of the first edition of this work, Mr. Sclater has published (‘Proc. Zoolog. Soc.’ 1868 page 623) a list of the species of mammals which have bred in the gardens from 1848 to 1867 inclusive. Of the Artiodactyla 85 species have been kept, and of these 1 species in 1.9 have bred at least once during the 20 years; of 28 Marsupialia, 1 in 2.5 have bred; of 74 Carnivora, 1 in 3.0 have bred; of 52 Rodentia, 1 in 4.7 have bred; and of Quadrumana 75 species have been kept, and 1 in 6.2 have bred.) Many facts are given on the breeding of the animals in that magnificent work, ‘Gleanings from the Menageries of Knowsley Hall’ by Dr. Gray. I made, also, particular inquiries from the experienced keeper of the birds in the old Surrey Zoological Gardens. I should premise that a slight change in the treatment of animals sometimes makes a great difference in their fertility; and it is probable that the results observed in different menageries would differ. Indeed, some animals in our Zoological Gardens have become more productive since the year 1846. It is, also, manifest from F. Cuvier’s account of the Jardin des Plantes (18/11. Du Rut ‘Annales du Museum’ 1807 tome 9 page 120.) that the animals formerly bred much less freely there than with us; for instance, in the Duck tribe, which is highly prolific, only one species had at that period produced young.
The most remarkable cases, however, are afforded by animals kept in their native country, which, though perfectly tamed, quite healthy, and allowed some freedom, are absolutely incapable of breeding. Rengger (18/12. ‘Saugethiere von Paraguay’ 1830 s. 49, 106, 118, 124, 201, 208, 249, 265, 327.), who in Paraguay particularly attended to this subject, specifies six quadrupeds in this condition; and he mentions two or three others which most rarely breed. Mr. Bates, in his admirable work on the Amazons, strongly insists on similar cases (18/13. ‘The Naturalist on the Amazons’ 1863 volume 1 pages 99, 193; volume 2 page 113.); and he remarks, that the fact of thoroughly tamed native mammals and birds not breeding when kept by the Indians, cannot be wholly accounted for by their negligence or indifference, for the turkey and fowl are kept and bred by various remote tribes. In almost every part of the world–for instance, in the interior of Africa, and in several of the Polynesian islands –the natives are extremely fond of taming the indigenous quadrupeds and birds; but they rarely or never succeed in getting them to breed.
The most notorious case of an animal not breeding in captivity is that of the elephant. Elephants are kept in large numbers in their native Indian home, live to old age, and are vigorous enough for the severest labour; yet, with a very few exceptions, they have never been known even to couple, though both males and females have their proper periodical seasons. If, however, we proceed a little eastward to Ava, we hear from Mr. Crawfurd (18/14. ‘Embassy to the Court of Ava’ volume 1 page 534.) that their “breeding in the domestic state, or at least in the half-domestic state in which the female elephants are generally kept, is of everyday occurrence;” and Mr. Crawfurd informs me that he believes that the difference must be attributed solely to the females being allowed to roam the forest with some degree of freedom. The captive rhinoceros, on the other hand, seems from Bishop Heber’s account (18/15. ‘Journal’ volume 1 page 213.) to breed in India far more readily than the elephant. Four wild species of the horse genus have bred in Europe, though here exposed to a great change in their natural habits of life; but the species have generally been crossed one with another. Most of the members of the pig family breed readily in our menageries; even the Red River hog (Potamochoerus penicillatus), from the sweltering plains of West Africa, has bred twice in the Zoological Gardens. Here also the Peccary (Dicotyles torquatus) has bred several times; but another species, the D. labiatus, though rendered so tame as to be half-domesticated, is said to breed so rarely in its native country of Paraguay, that according to Rengger (18/16. ‘Saugethiere’ s. 327.) the fact requires confirmation. Mr. Bates remarks that the tapir, though often kept tame in Amazonia by the Indians, never breeds.
Ruminants generally breed quite freely in England, though brought from widely different climates, as may be seen in the Annual Reports of the Zoological Gardens, and in the Gleanings from Lord Derby’s menagerie.
The Carnivora, with the exception of the Plantigrade division, breed (though with capricious exceptions) about half as freely as ruminants. Many species of Felidae have bred in various menageries, although imported from diverse climates and closely confined. Mr. Bartlett, the present superintendent of the Zoological Gardens (18/17. On the Breeding of the Larger Felidae ‘Proc. Zoolog. Soc.’ 1861 page 140.) remarks that the lion appears to breed more frequently and to bring forth more young at a birth than any other species of the family. He adds that the tiger has rarely bred; “but there are several well-authenticated instances of the female tiger breeding with the lion.” Strange as the fact may appear, many animals under confinement unite with distinct species and produce hybrids quite as freely as, or even more freely than, with their own species. On inquiring from Dr. Falconer and others, it appears that the tiger when confined in India does not breed, though it has been known to couple. The chetah (Felis jubata) has never been known by Mr. Bartlett to breed in England, but it has bred at Frankfort; nor does it breed in India, where it is kept in large numbers for hunting; but no pains would be taken to make them breed, as only those animals which have hunted for themselves in a state of nature are serviceable and worth training. (18/18. Sleeman’s ‘Rambles in India’ volume 2 page 10.) According to Rengger, two species of wild cats in Paraguay, though thoroughly tamed, have never bred. Although so many of the Felidae breed readily in the Zoological Gardens, yet conception by no means always follows union: in the nine-year Report, various species are specified which were observed to couple seventy-three times, and no doubt this must have passed many times unnoticed; yet from the seventy- three unions only fifteen births ensued. The Carnivora in the Zoological Gardens were formerly less freely exposed to the air and cold than at present, and this change of treatment, as I was assured by the former superintendent, Mr. Miller, greatly increased their fertility. Mr. Bartlett, and there cannot be a more capable judge, says, “it is remarkable that lions breed more freely in travelling collections than in the Zoological Gardens; probably the constant excitement and irritation produced by moving from place to place, or change of air, may have considerable influence in the matter.”
Many members of the Dog family breed readily when confined. The Dhole is one of the most untamable animals in India, yet a pair kept there by Dr. Falconer produced young. Foxes, on the other hand, rarely breed, and I have never heard of such an occurrence with the European fox: the silver fox of North America (Canis argentatus), however, has bred several times in the Zoological Gardens. Even the otter has bred there. Every one knows how readily the semi- domesticated ferret breeds, though shut up in miserably small cages; but other species of Viverra and Paradoxurus absolutely refuse to breed in the Zoological Gardens. The Genetta has bred both here and in the Jardin des Plantes, and produced hybrids. The Herpestes fasciatus has likewise bred; but I was formerly assured that the H. griseus, though many were kept in the Gardens, never bred.
The Plantigrade Carnivora breed under confinement much less freely than other Carnivora, although no reason can be assigned for this fact. In the nine-year Report it is stated that the bears had been seen in the Zoological Gardens to couple freely, but previously to 1848 had most rarely conceived. In the Reports published since this date three species have produced young (hybrids in one case), and, wonderful to relate, the white Polar bear has produced young. The badger (Meles taxus) has bred several times in the Gardens; but I have not heard of this occurring elsewhere in England, and the event must be very rare, for an instance in Germany has been thought worth recording. (18/19. Wiegmann ‘Archiv. fur Naturgesch.’ 1837 s. 162.) In Paraguay the native Nasua, though kept in pairs during many years and perfectly tamed, has never been known, according to Rengger, to breed or show any sexual passion; nor, as I hear from Mr. Bates, does this animal, or the Cercoleptes, breed in Amazonia. Two other plantigrade genera, Procyon and Gulo, though often kept tame in Paraguay, never breed there. In the Zoological Gardens species of Nasua and Procyon have been seen to couple; but they did not produce young.
As domesticated rabbits, guinea-pigs, and white mice breed so abundantly when closely confined under various climates, it might have been thought that most other members of the Rodent order would have bred in captivity, but this is not the case. It deserves notice, as showing how the capacity to breed sometimes goes by affinity, that the one native rodent of Paraguay, which there breeds FREELY and has yielded successive generations, is the Cavia aperea; and this animal is so closely allied to the guinea-pig, that it has been erroneously thought to be the parent form. (18/20. Rengger ‘Saugethiere’ etc. s. 276. On the parentage of the guinea-pig, see also Isid. Geoffroy St.- Hilaire ‘Hist. Nat. Gen.’ I sent to Mr. H. Denny of Leeds the lice which I collected from the wild aperea in La Plata, and he informs me that they belong to a genus distinct from those found on the guinea-pig. This is important evidence that the aperea is not the parent of the guinea-pig; and is worth giving, as some authors erroneously suppose that the guinea-pig since being domesticated has become sterile when crossed with the aperea.) In the Zoological Gardens, some rodents have coupled, but have never produced young; some have neither coupled nor bred; but a few have bred, as the porcupine more than once, the Barbary mouse, lemming, chinchilla, and agouti (Dasyprocta aguti) several times. This latter animal has also produced young in Paraguay, though they were born dead and ill-formed; but in Amazonia, according to Mr. Bates, it never breeds, though often kept tame about the houses. Nor does the paca (Coelogenys paca) breed there. The common hare when confined has, I believe, never bred in Europe; though, according to a recent statement, it has crossed with the rabbit. (18/21. Although the existence of the Leporides, as described by Dr. Broca (‘Journal de Phys.’ tome 2 page 370), has been positively denied, yet Dr. Pigeaux (‘Annals and Mag. of Nat. Hist.’ volume 20 1867 page 75) affirms that the hare and rabbit have produced hybrids.) I have never heard of the dormouse breeding in confinement. But squirrels offer a more curious case: with one exception, no species has bred in the Zoological Gardens, yet as many as fourteen individuals of S. palmarum were kept together during several years. The S. cinera has been seen to couple, but it did not produce young; nor has this species, when rendered extremely tame in its native country, North America, been ever known to breed. (18/22. ‘Quadrupeds of North America’ by Audubon and Bachman 1846 page 268.) At Lord Derby’s menagerie squirrels of many kinds were kept in numbers, but Mr. Thompson, the superintendent, told me that none had ever bred there, or elsewhere as far as he knew. I have never heard of the English squirrel breeding in confinement. But the species which has bred more than once in the Zoological Gardens is the one which perhaps might have been least expected, namely, the flying squirrel (Sciuropterus volucella): it has, also, bred several times near Birmingham; but the female never produced more than two young at a birth, whereas in its native American home she bears from three to six young. (18/23. Loudon’s ‘Mag. of Nat. Hist.’ volume 9 1836 page 571; Audubon and Bachman ‘Quadrupeds of North America’ page 221.)
Monkeys, in the nine-year Report from the Zoological Gardens, are stated to unite most freely, but during this period, though many individuals were kept, there were only seven births. I have heard of only one American monkey, the Ouistiti, breeding in Europe. (18/24. Flourens ‘De l’Instinct’ etc. 1845 page 88.) A Macacus, according to Flourens, bred in Paris; and more than one species of this genus has produced young in London, especially the Macacus rhesus, which everywhere shows a special capacity to breed under confinement. Hybrids have been produced both in Paris and London from this same genus. The Arabian baboon, or Cynocephalus hamadryas (18/25. See ‘Annual Reports Zoolog. Soc.’ 1855, 1858, 1863, 1864; ‘Times’ newspaper August 10, 1847; Flourens ‘De l’Instinct’ page 85.), and a Cercopithecus have bred in the Zoological Gardens, and the latter species at the Duke of Northumberland’s. Several members of the family of Lemurs have produced hybrids in the Zoological Gardens. It is much more remarkable that monkeys very rarely breed when confined in their native country; thus the Cay (Cebus azara) is frequently and completely tamed in Paraguay, but Rengger (18/26. ‘Saugethiere’ etc. s. 34, 49.) says that it breeds so rarely, that he never saw more than two females which had produced young. A similar observation has been made with respect to the monkeys which are frequently tamed by the aborigines in Brazil. (18/27. Art. Brazil ‘Penny Cyclop.’ page 363.) In Amazonia, these animals are so often kept in a tame state, that Mr. Bates in walking through the streets of Para counted thirteen species; but, as he asserts, they have never been known to breed in captivity. (18/28. ‘The Naturalist on the Amazons’ volume 1 page 99.)
BIRDS.
Birds offer in some respects better evidence than quadrupeds, from their breeding more rapidly and being kept in greater numbers. (18/29. A list of the species of birds which have bred in the Zoological Gardens from 1848 to 1867 inclusive has been published by Mr. Sclater in ‘Proc. Zoolog. Soc.’ 1869 page 626, since the first edition of this work appeared. Of Columbae 51 species have been kept, and of Anseres 80 species, and in both these families 1 species in 2.6 have bred at least once in the 20 years. Of Gallinae 83 species have been kept and 1 in 27 have bred; of 57 Grallae 1 in 9 have bred; of 110 Prehensores 1 in 22 have bred; of 178 Passeres 1 in 25.4 have bred; of 94 Accipitres 1 in 47 have bred; of 25 Picariae and of 35 Herodiones not one species in either group has bred.) We have seen that carnivorous animals are more fertile under confinement than most other mammals. The reverse holds good with carnivorous birds. It is said (18/30. ‘Encyclop. of Rural Sports’ page 691.) that as many as eighteen species have been used in Europe for hawking, and several others in Persia and India (18/31. According to Sir A. Burnes ‘Cabool’ etc. page 51, eight species are used for hawking in Sinde.); they have been kept in their native country in the finest condition, and have been flown during six, eight, or nine years (18/32. Loudon’s ‘Mag. of Nat. Hist.’ volume 6 1833 page 110.); yet there is no record of their having ever produced young. As these birds were formerly caught whilst young, at great expense, being imported from Iceland, Norway, and Sweden, there can be little doubt that, if possible, they would have been propagated. In the Jardin des Plantes, no bird of prey has been known to couple. (18/33. F. Cuvier ‘Annal. du Museum’ tome 9 page 128.) No hawk, vulture, or owl has ever produced fertile eggs in the Zoological Gardens, or in the old Surrey Gardens, with the exception, in the former place on one occasion, of a condor and a kite (Milvus niger). Yet several species, namely, the Aquila fusca, Haliaetus leucocephalus, Falco tinnunculus, F. subbuteo, and Buteo vulgaris, have been seen to couple in the Zoological Gardens. Mr. Morris (18/34. ‘The Zoologist’ volume 7-8 1849-50 page 2648.) mentions as a unique fact that a kestrel (Falco tinnunculus) bred in an aviary. The one kind of owl which has been known to couple in the Zoological Gardens was the Eagle Owl (Bubo maximus); and this species shows a special inclination to breed in captivity; for a pair at Arundel Castle, kept more nearly in a state of nature “than ever fell to the lot of an animal deprived of its liberty” (18/35. Knox ‘Ornithological Rambles in Sussex’ page 91.), actually reared their young. Mr. Gurney has given another instance of this same owl breeding in confinement; and he records the case of a second species of owl, the Strix passerina, breeding in captivity. (18/36. ‘The Zoologist’ volume 7-8 1849-50 page 2566; volume 9-10 1851-2 page 3207.)
Of the smaller graminivorous birds, many kinds have been kept tame in their native countries, and have lived long; yet, as the highest authority on cage- birds (18/37. Bechstein ‘Naturgesch. der Stubenvogel’ 1840 s. 20.) remarks, their propagation is “uncommonly difficult.” The canary-bird shows that there is no inherent difficulty in these birds breeding freely in confinement; and Audubon says (18/38. ‘Ornithological Biography’ volume 5 page 517.) that the Fringilla (Spiza) ciris of North America breeds as perfectly as the canary. The difficulty with the many finches which have been kept in confinement is all the more remarkable as more than a dozen species could be named which have yielded hybrids with the canary; but hardly any of these, with the exception of the siskin (Fringilla spinus), have reproduced their own kind. Even the bullfinch (Loxia pyrrhula) has bred as frequently with the canary, though belonging to a distinct genus, as with its own species. (18/39. A case is recorded in ‘The Zoologist’ volume 1-2 1843-45 page 453. For the siskin breeding, volume 3-4 1845-46 page 1075. Bechstein ‘Stubenvogel’ s. 139 speaks of bullfinches making nests, but rarely producing young.) With respect to the skylark (Alauda arvensis), I have heard of birds living for seven years in an aviary, which never produced young; and a great London bird-fancier assured me that he had never known an instance of their breeding; nevertheless one case has been recorded. (18/40. Yarrell ‘Hist. British Birds’ 1839 volume 1 page 412.) In the nine-year Report from the Zoological Society, twenty-four insessorial species are enumerated which had not bred, and of these only four were known to have coupled.
Parrots are singularly long-lived birds; and Humboldt mentions the curious fact of a parrot in South America, which spoke the language of an extinct Indian tribe, so that this bird preserved the sole relic of a lost language. Even in this country there is reason to believe (18/41. Loudon’s ‘Mag. of Nat. History’ volume 19 1836 page 347.) that parrots have lived to the age of nearly one hundred years; yet they breed so rarely, though many have been kept in Europe, that the event has been thought worth recording in the gravest publications. (18/42. ‘Memoires du Museum d’Hist. Nat.’ tome 10 page 314: five cases of parrots breeding in France are here recorded. See also ‘Report Brit. Assoc. Zoolog.’ 1843.) Nevertheless, when Mr. Buxton turned out a large number of parrots in Norfolk, three pairs bred and reared ten young birds in the course of two seasons; and this success may be attributed to their free life. (18/43. ‘Annals and Mag. of Nat. Hist.’ November 1868 page 311.) According to Bechstein (18/44. ‘Stubenvogel’ s. 105, 83.) the African Psittacus erithacus breeds oftener than any other species in Germany: the P. macoa occasionally lays fertile eggs, but rarely succeeds in hatching them; this bird, however, has the instinct of incubation sometimes so strongly developed, that it will hatch the eggs of fowls or pigeons. In the Zoological Gardens and in the old Surrey Gardens some few species have coupled, but, with the exception of three species of parakeets, none have bred. It is a much more remarkable fact that in Guiana parrots of two kinds, as I am informed by Sir R. Schomburgk, are often taken from the nests by the Indians and reared in large numbers; they are so tame that they fly freely about the houses, and come when called to be fed, like pigeons; yet he has never heard of a single instance of their breeding. (18/45. Dr. Hancock remarks (‘Charlesworth’s Mag. of Nat. Hist.’ volume 2 1838 page 492) “it is singular that, amongst the numerous useful birds that are indigenous to Guiana, none are found to propagate among the Indians; yet the common fowl is reared in abundance throughout the country.”) In Jamaica, a resident naturalist, Mr. R. Hill (18/46. ‘A Week at Pert Royal’ 1855 page 7.), says, “no birds more readily submit to human dependence than the parrot-tribe, but no instance of a parrot breeding in this tame life has been known yet.” Mr. Hill specifies a number of other native birds kept tame in the West Indies, which never breed in this state.
The great pigeon family offers a striking contrast with the parrots: in the nine-year Report thirteen species are recorded as having bred, and, what is more noticeable, only two were seen to couple without any result. Since the above date every annual Report gives many cases of various pigeons breeding. The two magnificent crowned pigeons (Goura coronata and victoriae) produced hybrids; nevertheless, of the former species more than a dozen birds were kept, as I am informed by Mr. Crawfurd, in a park at Penang, under a perfectly well-adapted climate, but never once bred. The Columba migratoria in its native country, North America, invariably lays two eggs, but in Lord Derby’s menagerie never more than one. The same fact has been observed with the C. leucocephala. (18/47. Audubon ‘American Ornithology’ volume 5 pages 552, 557.)
Gallinaceous birds of many genera likewise show an eminent capacity for breeding under captivity. This is particularly the case with pheasants, yet our English species seldom lays more than ten eggs in confinement; whilst from eighteen to twenty is the usual number in the wild state. (18/48. Mowbray on ‘Poultry’ 7th edition page 133.) With the Gallinaceae, as with all other orders, there are marked and inexplicable exceptions in regard to the fertility of certain species and genera under confinement. Although many trials have been made with the common partridge, it has rarely bred, even when reared in large aviaries; and the hen will never hatch her own eggs. (18/49. Temminck ‘Hist. Nat. Gen. des Pigeons’ etc. 1813 tome 3 pages 288, 382; ‘Annals and Mag. of Nat. Hist.’ volume 12 1843 page 453. Other species of partridge have occasionally bred; as the red-legged (P. rubra), when kept in a large court in France (see Journal de Physique’ tome 25 page 294), and in the Zoological Gardens in 1856.) The American tribe of Guans or Cracidae are tamed with remarkable ease, but are very shy breeders in this country (18/50. Rev. E.S. Dixon ‘The Dovecote’ 1851 pages 243-252.); but with care various species were formerly made to breed rather freely in Holland. (18/51. Temminck ‘Hist. Nat. Gen. des Pigeons’ etc. tome 2 pages 456, 458; tome 3 pages 2, 13, 47.) Birds of this tribe are often kept in a perfectly tamed condition in their native country by the Indians, but they never breed. (18/52. Bates ‘The Naturalist on the Amazons’ volume 1 page 193; volume 2 page 112.) It might have been expected that grouse from their habits of life would not have bred in captivity, more especially as they are said soon to languish and die. (18/53. Temminck ‘Hist. Nat. Gen.’ etc. tome 2 page 125. For Tetrao urogallus see L. Lloyd ‘Field Sports of North of Europe’ volume 1 pages 287, 314; and Bull. de la Soc. d’Acclimat.’ tome 7 1860 page 600. For T. scoticus Thompson ‘Nat. Hist. of Ireland’ volume 2 1850 page 49. For T. cupido ‘Boston Journal of Nat. Hist.’ volume 3 page 199.) But many cases are recorded of their breeding: the capercailzie (Tetrao urogallus) has bred in the Zoological Gardens; it breeds without much difficulty when confined in Norway, and in Russia five successive generations have been reared: Tetrao tetrix has likewise bred in Norway; T. scoticus in Ireland; T. umbellus at Lord Derby’s; and T. cupido in North America.
It is scarcely possible to imagine a greater change in habits than that which the members of the ostrich family must suffer, when cooped up in small enclosures under a temperate climate, after freely roaming over desert and tropical plains or entangled forests; yet almost all the kinds have frequently produced young in the various European menageries, even the mooruk (Casuarius bennetii) from New Ireland. The African ostrich, though perfectly healthy and living long in the South of France, never lays more than from twelve to fifteen eggs, though in its native country it lays from twenty-five to thirty. (18/54. Marcel de Serres ‘Annales des Sc. Nat.’ 2nd series Zoolog. tome 13 page 175.) Here we have another instance of fertility impaired, but not lost, under confinement, as with the flying squirrel, the hen-pheasant, and two species of American pigeons.
Most Waders can be tamed, as the Rev. E.S. Dixon informs me, with remarkable facility; but several of them are short-lived under confinement, so that their sterility in this state is not surprising. The cranes breed more readily than other genera: Grus montigresia has bred several times in Paris and in the Zoological Gardens, as has G. cinerea at the latter place, and G. antigone at Calcutta. Of other members of this great order, Tetrapteryx paradisea has bred at Knowsley, a Porphyrio in Sicily, and the Gallinula chloropus in the Zoological Gardens. On the other hand, several birds belonging to this order will not breed in their native country, Jamaica; and the Psophia, though often kept by the Indians of Guiana about their houses, “is seldom or never known to breed.” (18/55. Dr. Hancock in ‘Charlesworth’s Mag. of Nat. Hist.’ volume 2 1838 page 491; R. Hill ‘A Week at Port Royal’ page 8; ‘Guide to the Zoological Gardens’ by P.L. Sclater 1859 pages 11, 12; ‘The Knowsley Menagerie’ by D. Gray 1846 p1. 14; E. Blyth ‘Report Asiatic Soc. of Bengal’ May 1855.)
The members of the great Duck family breed as readily in confinement as do the Columbae and Gallinae and this, considering their aquatic and wandering habits, and the nature of their food, could not have been anticipated. Even some time ago above two dozen species had bred in the Zoological Gardens; and M. Selys-Longchamps has recorded the production of hybrids from forty-four different members of the family; and to these Professor Newton has added a few more cases. (18/56. Prof. Newton in ‘Proc. Zoolog. Soc.’ 1860 page 336.) “There is not,” says Mr. Dixon (18/57. ‘The Dovecote and Aviary’ page 428.), “in the wide world, a goose which is not in the strict sense of the word domesticable;” that is, capable of breeding under confinement; but this statement is probably too bold. The capacity to breed sometimes varies in individuals of the same species; thus Audubon (18/58. ‘Ornithological Biography’ volume 3 page 9.) kept for more than eight years some wild geese (Anser canadensis), but they would not mate; whilst other individuals of the same species produced young during the second year. I know of but one instance in the whole family of a species which absolutely refuses to breed in captivity, namely, the Dendrocygna viduata, although, according to Sir R. Schomburgk (18/59. ‘Geograph. Journal’ volume 13 1844 page 32.), it is easily tamed, and is frequently kept by the Indians of Guiana. Lastly, with respect to Gulls, though many have been kept in the Zoological Gardens and in the old Surrey Gardens, no instance was known before the year 1848 of their coupling or breeding; but since that period the herring gull (Larus argentatus) has bred many times in the Zoological Gardens and at Knowsley.
There is reason to believe that insects are affected by confinement like the higher animals. It is well known that the Sphingidae rarely breed when thus treated. An entomologist (18/60. Loudon’s ‘Mag. of Nat. Hist.’ volume 5 1832 page 153.) in Paris kept twenty-five specimens of Saturnia pyri, but did not succeed in getting a single fertile egg. A number of females of Orthosia munda and of Mamestra suasa reared in confinement were unattractive to the males. (18/61. ‘Zoologist’ volumes 5-6 1847-48 page 1660.) Mr. Newport kept nearly a hundred individuals of two species of Vanessa, but not one paired; this, however, might have been due to their habit of coupling on the wing. (18/62. ‘Transact. Entomolog. Soc.’ volume 4 1845 page 60.) Mr. Atkinson could never succeed in India in making the Tarroo silk-moth breed in confinement. (18/63. ‘Transact. Linn. Soc.’ volume 7 page 40.) It appears that a number of moths, especially the Sphingidae, when hatched in the autumn out of their proper season, are completely barren; but this latter case is still involved in some obscurity. (18/64. See an interesting paper by Mr. Newman in the ‘Zoologist’ 1857 page 5764; and Dr. Wallace in ‘Proc. Entomolog. Soc.’ June 4, 1860 page 119.)
Independently of the fact of many animals under confinement not coupling, or, if they couple, not producing young, there is evidence of another kind that their sexual functions are disturbed. For many cases have been recorded of the loss by male birds when confined of their characteristic plumage. Thus the common linnet (Linota cannabina) when caged does not acquire the fine crimson colour on its breast, and one of the buntings (Emberiza passerina) loses the black on its head. A Pyrrhula and an Oriolus have been observed to assume the quiet plumage of the hen-bird; and the Falco albidus returned to the dress of an earlier age. (18/65. Yarrell ‘British Birds’ volume 1 page 506; Bechstein ‘Stubenvogel’ s. 185; ‘Philosoph. Transact.’ 1772 page 271. Bronn ‘Geschichte der Natur’ b. 2 s. 96 has collected a number of cases. For the case of the deer see ‘Penny Cyclop.’ volume 8 page 350.) Mr. Thompson, the superintendent of the Knowsley menagerie, informed me that he had often observed analogous facts. The horns of a male deer (Cervus canadensis) during the voyage from America were badly developed; but subsequently in Paris perfect horns were produced.
When conception takes place under confinement, the young are often born dead, or die soon, or are ill-formed. This frequently occurs in the Zoological Gardens, and, according to Rengger, with native animals confined in Paraguay. The mother’s milk often fails. We may also attribute to the disturbance of the sexual functions the frequent occurrence of that monstrous instinct which leads the mother to devour her own offspring,–a mysterious case of perversion, as it at first appears.
Sufficient evidence has now been advanced to prove that animals when first confined are eminently liable to suffer in their reproductive systems. We feel at first naturally inclined to attribute the result to loss of health, or at least to loss of vigour; but this view can hardly be admitted when we reflect how healthy, long-lived, and vigorous many animals are under captivity, such as parrots, and hawks when used for hawking, cheetahs when used for hunting, and elephants. The reproductive organs themselves are not diseased; and the diseases, from which animals in menageries usually perish, are not those which in any way affect their fertility. No domestic animal is more subject to disease than the sheep, yet it is remarkably prolific. The failure of animals to breed under confinement has been sometimes attributed exclusively to a failure in their sexual instincts: this may occasionally come into play, but there is no obvious reason why this instinct should be especially liable to be affected with perfectly tamed animals, except, indeed, indirectly through the reproductive system itself being disturbed. Moreover, numerous cases have been given of various animals which couple freely under confinement, but never conceive; or, if they conceive and produce young, these are fewer in number than is natural to the species. In the vegetable kingdom instinct of course can play no part; and we shall presently see that plants when removed from their natural conditions are affected in nearly the same manner as animals. Change of climate cannot be the cause of the loss of fertility, for, whilst many animals imported into Europe from extremely different climates breed freely, many others when confined in their native land are completely sterile. Change of food cannot be the chief cause; for ostriches, ducks, and many other animals, which must have undergone a great change in this respect, breed freely. Carnivorous birds when confined are extremely sterile, whilst most carnivorous mammals, except plantigrades, are moderately fertile. Nor can the amount of food be the cause; for a sufficient supply will certainly be given to valuable animals; and there is no reason to suppose that much more food would be given to them than to our choice domestic productions which retain their full fertility. Lastly, we may infer from the case of the elephant, cheetah, various hawks, and of many animals which are allowed to lead an almost free life in their native land, that want of exercise is not the sole cause.
It would appear that any change in the habits of life, whatever these habits may be, if great enough, tends to affect in an inexplicable manner the powers of reproduction. The result depends more on the constitution of the species than on the nature of the change; for certain whole groups are affected more than others; but exceptions always occur, for some species in the most fertile groups refuse to breed, and some in the most sterile groups breed freely. Those animals which usually breed freely under confinement, rarely breed, as I was assured, in the Zoological Gardens, within a year or two after their first importation. When an animal which is generally sterile under confinement happens to breed, the young apparently do not inherit this power: for had this been the case, various quadrupeds and birds, which are valuable for exhibition, would have become common. Dr. Broca even affirms (18/66. ‘Journal de Physiologie’ tome 2 page 347.) that many animals in the Jardin des Plantes, after having produced young for three or four successive generations, become sterile; but this may be the result of too close interbreeding. It is a remarkable circumstance that many mammals and birds have produced hybrids under confinement quite as readily as, or even more readily than, they have procreated their own kind. Of this fact many instances have been given (18/67. For additional evidence on this subject see F. Cuvier in ‘Annales du Museum’ tome 12 page 119.); and we are thus reminded of those plants which when cultivated refuse to be fertilised by their own pollen, but can easily be fertilised by that of a distinct species. Finally, we must conclude, limited as the conclusion is, that changed conditions of life have an especial power of acting injuriously on the reproductive system. The whole case is quite peculiar, for these organs, though not diseased, are thus rendered incapable of performing their proper functions, or perform them imperfectly.
STERILITY OF DOMESTICATED ANIMALS FROM CHANGED CONDITIONS. — With respect to domesticated animals, as their domestication mainly depends on the accident of their breeding freely under captivity, we ought not to expect that their reproductive system would be affected by any moderate degree of change. Those orders of quadrupeds and birds, of which the wild species breed most readily in our menageries, have afforded us the greatest number of domesticated productions. Savages in most parts of the world are fond of taming animals (18/68. Numerous instances could be given. Thus Livingstone (‘Travels’ page 217) states that the King of the Barotse, an inland tribe which never had any communication with white men, was extremely fond of taming animals, and every young antelope was brought to him. Mr. Galton informs me that the Damaras are likewise fond of keeping pets. The Indians of South America follow the same habit. Capt. Wilkes states that the Polynesians of the Samoan Islands tamed pigeons; and the New Zealanders, as Mr. Mantell informs me, kept various kinds of birds.); and if any of these regularly produced young, and were at the same time useful, they would be at once domesticated. If, when their masters migrated into other countries, they were in addition found capable of withstanding various climates, they would be still more valuable; and it appears that the animals which breed readily in captivity can generally withstand different climates. Some few domesticated animals, such as the reindeer and camel, offer an exception to this rule. Many of our domesticated animals can bear with undiminished fertility the most unnatural conditions; for instance, rabbits, guinea-pigs, and ferrets breed in miserably confined hutches. Few European dogs of any kind withstand the climate of India without degenerating, but as long as they survive, they retain, as I hear from Dr. Falconer, their fertility; so it is, according to Dr. Daniell, with English dogs taken to Sierra Leone. The fowl, a native of the hot jungles of India, becomes more fertile than its parent-stock in every quarter of the world, until we advance as far north as Greenland and Northern Siberia, where this bird will not breed. Both fowls and pigeons, which I received during the autumn direct from Sierra Leone, were at once ready to couple. (18/69. For analogous cases with the fowl see Reaumur ‘L’Art de faire Eclore’ etc. 1749 page 243; and Col. Sykes in ‘Proc. Zoolog. Soc.’ 1832 etc. With respect to the fowl not breeding in northern regions see Latham ‘Hist. of Birds’ volume 8 1823 page 169.) I have, also, seen pigeons breeding as freely as the common kinds within a year after their importation from the upper Nile. The guinea- fowl, an aboriginal of the hot and dry deserts of Africa, whilst living under our damp and cool climate, produces a large supply of eggs.
Nevertheless, our domesticated animals under new conditions occasionally show signs of lessened fertility. Roulin asserts that in the hot valleys of the equatorial Cordillera sheep are not fully fecund (18/70. “Mem. par divers Savans” ‘Acad. des Sciences’ tome 6 1835 page 347.); and according to Lord Somerville (18/71. ‘Youatt on Sheep’ page 181.) the merino-sheep which he imported from Spain were not at first perfectly fertile, it is said (18/72. J. Mills ‘Treatise on Cattle’ 1776 page 72.) that mares brought up on dry food in the stable, and turned out to grass, do not at first breed. The peahen, as we have seen, is said not to lay so many eggs in England as in India. It was long before the canary-bird was fully fertile, and even now first-rate breeding birds are not common. (18/73. Bechstein ‘Stubenvogel’ s. 242.) In the hot and dry province of Delhi, as I hear from Dr. Falconer, the eggs of the turkey, though placed under a hen, are extremely liable to fail. According to Roulin, geese taken to the lofty plateau of Bogota, at first laid seldom, and then only a few eggs; of these scarcely a fourth were hatched, and half the young birds died; in the second generation they were more fertile; and when Roulin wrote they were becoming as fertile as our geese in Europe. With respect to the valley of Quito, Mr. Orton says (18/74. ‘The Andes and the Amazon’ 1870 page 107.) “the only geese in the valley are a few imported from Europe, and these refuse to propagate.” In the Philippine Archipelago the goose, it is asserted, will not breed or even lay eggs. (18/75. Crawford ‘Descriptive Dict. of the Indian Islands’ 1856 page 145.) A more curious case is that of the fowl, which, according to Roulin, when first introduced would not breed at Cusco in Bolivia, but subsequently became quite fertile; and the English Game fowl, lately introduced, had not as yet arrived at its full fertility, for to raise two or three chickens from a nest of eggs was thought fortunate. In Europe close confinement has a marked effect on the fertility of the fowl: it has been found in France that with fowls allowed considerable freedom only twenty per cent of the eggs failed; when allowed less freedom forty per cent failed; and in close confinement sixty out of the hundred were not hatched. (18/76. ‘Bull. de la Soc. d’Acclimat.’ tome 9 1862 pages 380, 384.) So we see that unnatural and changed conditions of life produce some effect on the fertility of our most thoroughly domesticated animals, in the same manner, though in a far less degree, as with captive wild animals.
It is by no means rare to find certain males and females which will not breed together, though both are known to be perfectly fertile with other males and females. We have no reason to suppose that this is caused by these animals having been subjected to any change in their habits of life; therefore such cases are hardly related to our present subject. The cause apparently lies in an innate sexual incompatibility of the pair which are matched. Several instances have been communicated to me by Mr. W.C. Spooner (well known for his essay on Cross-breeding), by Mr. Eyton of Eyton, by Mr. Wicksted and other breeders, and especially by Mr. Waring of Chelsfield, in relation to horses, cattle, pigs, foxhounds, other dogs, and pigeons. (18/77. For pigeons see Dr. Chapuis ‘Le Pigeon Voyageur Belge’ 1865 page 66.) In these cases, females, which either previously or subsequently were proved to be fertile, failed to breed with certain males, with whom it was particularly desired to match them. A change in the constitution of the female may sometimes have occurred before she was put to the second male; but in other cases this explanation is hardly tenable, for a female, known not to be barren, has been unsuccessfully paired seven or eight times with the same male likewise known to be perfectly fertile. With cart-mares, which sometimes will not breed with stallions of pure blood, but subsequently have bred with cart-stallions, Mr. Spooner is inclined to attribute the failure to the lesser sexual power of the racehorse. But I have heard from the greatest breeder of racehorses at the present day, through Mr. Waring, that “it frequently occurs with a mare to be put several times during one or two seasons to a particular stallion of acknowledged power, and yet prove barren; the mare afterwards breeding at once with some other horse.” These facts are worth recording, as they show, like so many previous facts, on what slight constitutional differences the fertility of an animal often depends.
STERILITY OF PLANTS FROM CHANGED CONDITIONS OF LIFE, AND FROM OTHER CAUSES.
In the vegetable kingdom cases of sterility frequently occur, analogous with those previously given in the animal kingdom. But the subject is obscured by several circumstances, presently to be discussed, namely, the contabescence of the anthers, as Gartner has named a certain affection–monstrosities– doubleness of the flower–much-enlarged fruit–and long-continued or excessive propagation by buds.
It is notorious that many plants in our gardens and hot-houses, though preserved in the most perfect health, rarely or never produce seed. I do not allude to plants which run to leaves, from being kept too damp, or too warm, or too much manured; for these do not flower, and the case may be wholly different. Nor do I allude to fruit not ripening from want of heat or rotting from too much moisture. But many exotic plants, with their ovules and pollen appearing perfectly sound, will not set any seed. The sterility in many cases, as I know from my own observation, is simply due to the absence of the proper insects for carrying the pollen to the stigma. But after excluding the several cases just specified, there are many plants in which the reproductive system has been seriously affected by the altered conditions of life to which they have been subjected.
It would be tedious to enter on many details. Linnaeus long ago observed (18/78. ‘Swedish Acts’ volume 1 1739 page 3. Pallas makes the same remark in his ‘Travels’ English translation volume 1 page 292.) that Alpine plants, although naturally loaded with seed, produce either few or none when cultivated in gardens. But exceptions often occur: the Draba sylvestris, one of our most thoroughly Alpine plants, multiplies itself by seed in Mr. H.C. Watson’s garden, near London; and Kerner, who has particularly attended to the cultivation of Alpine plants, found that various kinds, when cultivated, spontaneously sowed themselves. (18/79. A. Kerner ‘Die Cultur der Alpenpflanzen’ 1864 s. 139; Watson ‘Cybele Britannica’ volume 1 page 131; Mr. D. Cameron also has written on the culture of Alpine plants in ‘Gard. Chronicle’ 1848 pages 253, 268, and mentions a few which seed.) Many plants which naturally grow in peat-earth are entirely sterile in our gardens. I have noticed the same fact with several liliaceous plants, which nevertheless grew vigorously.
Too much manure renders some kinds utterly sterile, as I have myself observed. The tendency to sterility from this cause runs in families; thus, according to Gartner (18/80. ‘Beitrage zur Kenntniss der Befruchtung’ 1844 s. 333.), it is hardly possible to give too much manure to most Gramineae, Cruciferae, and Leguminosae, whilst succulent and bulbous-rooted plants are easily affected. Extreme poverty of soil is less apt to induce sterility; but dwarfed plants of Trifolium minus and repens, growing on a lawn often mown and never manured, were found by me not to produce any seed. The temperature of the soil, and the season at which plants are watered, often have a marked effect on their fertility, as was observed by Kolreuter in the case of Mirabilis. (18/81. ‘Nova Acta Petrop.’ 1793 page 391.) Mr. Scott, in the Botanic Gardens of Edinburgh, observed that Oncidium divaricatum would not set seed when grown in a basket in which it throve, but was capable of fertilisation in a pot where it was a little damper. Pelargonium fulgidum, for many years after its introduction, seeded freely; it then became sterile; now it is fertile (18/82. ‘Cottage Gardener’ 1856 pages 44, 109.) if kept in a dry stove during the winter. Other varieties of pelargonium are sterile and others fertile without our being able to assign any cause. Very slight changes in the position of a plant, whether planted on a bank or at its base, sometimes make all the difference in its producing seed. Temperature apparently has a much more powerful influence on the fertility of plants than on that of animals. Nevertheless it is wonderful what changes some few plants will withstand with undiminished fertility: thus the Zephyranthes candida, a native of the moderately warm banks of the Plata, sows itself in the hot dry country near Lima, and in Yorkshire resists the severest frosts, and I have seen seeds gathered from pods which had been covered with snow during three weeks. (18/83. Dr. Herbert ‘Amaryllidaceae’ page 176.) Berberis wallichii, from the hot Khasia range in India, is uninjured by our sharpest frosts, and ripens its fruit under our cool summers. Nevertheless, I presume we must attribute to change of climate the sterility of many foreign plants; thus, the Persian and Chinese lilacs (Syringa persica and chinensis), though perfectly hardy here, never produce a seed; the common lilac (S. vulgaris) seeds with us moderately well, but in parts of Germany the capsules never contain seed. (18/84. Gartner ‘Beitrage zur Kenntniss’ etc. s. 560, 564.) Some few of the cases, given in the last chapter, of self-impotent plants, might have been here introduced, as their state seems due to the conditions to which they have been subjected.
The liability of plants to be affected in their fertility by slightly changed conditions is the more remarkable, as the pollen when once in process of formation is not easily injured; a plant may be transplanted, or a branch with flower-buds be cut off and placed in water, and the pollen will be matured. Pollen, also, when once mature, may be kept for weeks or even months. (18/85. ‘Gardener’s Chronicle’ 1844 page 215; 1850 page 470. Faivre gives a good resume on this subject in his ‘La Variabilite des Especes’ 1868 page 155.) The female organs are more sensitive, for Gartner (18/86. ‘Beitrage zur Kenntniss’ etc. s. 252, 338.) found that dicotyledonous plants, when carefully removed so that they did not in the least flag, could seldom be fertilised; this occurred even with potted plants if the roots had grown out of the hole at the bottom. In some few cases, however, as with Digitalis, transplantation did not prevent fertilisation; and according to the testimony of Mawz, Brassica rapa, when pulled up by its roots and placed in water, ripened its seed. Flower-stems of several monocotyledonous plants when cut off and placed in water likewise produce seed. But in these cases I presume that the flowers had been already fertilised, for Herbert (18/87. ‘Journal of Hort. Soc.’ volume 2 1847 page 83.) found with the Crocus that the plants might be removed or mutilated after the act of fertilisation, and would still perfect their seeds; but that, if transplanted before being fertilised, the application of pollen was powerless.
Plants which have been long cultivated can generally endure with undiminished fertility various and great changes; but not in most cases so great a change of climate as domesticated animals. It is remarkable that many plants under these circumstances are so much affected that the proportion and the nature of their chemical ingredients are modified, yet their fertility is unimpaired. Thus, as Dr. Falconer informs me, there is a great difference in the character of the fibre in hemp, in the quantity of oil in the seed of the Linum, in the proportion of narcotin to morphine in the poppy, in gluten to starch in wheat, when these plants are cultivated on the plains and on the mountains of India; nevertheless, they all remain fully fertile.
CONTABESCENCE. — Gartner has designated by this term a peculiar condition of the anthers in certain plants, in which they are shrivelled, or become brown and tough, and contain no good pollen. When in this state they exactly resemble the anthers of the most sterile hybrids. Gartner (18/88. ‘Beitrage zur Kenntniss’ etc. s. 117 et seq.; Kolreuter ‘Zweite Fortsetzung’ s. 10, 121; ‘Dritte Fortsetzung’ s. 57. Herbert ‘Amaryllidaceae’ page 355. Wiegmann ‘Ueber die Bastarderzeugung’ s. 27.), in his discussion on this subject, has shown that plants of many orders are occasionally thus affected; but the Caryophyllaceae and Liliaceae suffer most, and to these orders, I think, the Ericaceae may be added. Contabescence varies in degree, but on the same plant all the flowers are generally affected to nearly the same extent. The anthers are affected at a very early period in the flower-bud, and remain in the same state (with one recorded exception) during the life of the plant. The affection cannot be cured by any change of treatment, and is propagated by layers, cuttings, etc., and perhaps even by seed. In contabescent plants the female organs are seldom affected, or merely become precocious in their development. The cause of this affection is doubtful, and is different in different cases. Until I read Gartner’s discussion I attributed it, as apparently did Herbert, to the unnatural treatment of the plants; but its permanence under changed conditions, and the female organs not being affected, seem incompatible with this view. The fact of several endemic plants becoming contabescent in our gardens seems, at first sight, equally incompatible with this view; but Kolreuter believes that this is the result of their transplantation. The contabescent plants of Dianthus and Verbascum, found wild by Wiegmann, grew on a dry and sterile bank. The fact that exotic plants are eminently liable to this affection also seems to show that it is in some manner caused by their unnatural treatment. In some instances, as with Silene, Gartner’s view seems the most probable, namely, that it is caused by an inherent tendency in the species to become dioecious. I can add another cause, namely, the illegitimate unions of heterostyled plants, for I have observed seedlings of three species of Primula and of Lythrum salicaria, which had been raised from plants illegitimately fertilised by their own-form pollen, with some or all their anthers in a contabescent state. There is perhaps an additional cause, namely, self-fertilisation; for many plants of Dianthus and Lobelia, which had been raised from self-fertilised seeds, had their anthers in this state; but these instances are not conclusive, as both genera are liable from other causes to this affection.
Cases of an opposite nature likewise occur, namely, plants with the female organs struck with sterility, whilst the male organs remain perfect. Dianthus japonicus, a Passiflora, and Nicotiana, have been described by Gartner (18/89. ‘Bastarderzengung’ s. 356.) as being in this unusual condition.
MONSTROSITIES AS A CAUSE OF STERILITY. — Great deviations of structure, even when the reproductive organs themselves are not seriously affected, sometimes cause plants to become sterile. But in other cases plants may become monstrous to an extreme degree and yet retain their full fertility. Gallesio, who certainly had great experience (18/90. ‘Teoria della Riproduzione’ 1816 page 84; ‘Traite du Citrus’ 1811 page 67.), often attributes sterility to this cause; but it may be suspected that in some of his cases sterility was the cause, and not the result, of the monstrous growths. The curious St. Valery apple, although it bears fruit, rarely produces seed. The wonderfully anomalous flowers of Begonia frigida, formerly described, though they appear fit for fructification, are sterile. (18/91. Mr. C.W. Crocker in ‘Gardener’s Chronicle’ 1861 page 1092.) Species of Primula in which the calyx is brightly coloured are said (18/92. Verlot ‘Des Varietes’ 1865 page 80.) to be often sterile, though I have known them to be fertile. On the other hand, Verlot gives several cases of proliferous flowers which can be propagated by seed. This was the case with a poppy, which had become monopetalous by the union of its petals. (18/93. Verlot ibid page 88.) Another extraordinary poppy, with the stamens replaced by numerous small supplementary capsules, likewise reproduces itself by seed. This has also occurred with a plant of Saxifraga geum, in which a series of adventitious carpels, bearing ovules on their margins, had been developed between the stamens and the normal carpels (18/94. Prof. Allman, Brit. Assoc., quoted in the ‘Phytologist’ volume 2 page 483. Prof. Harvey, on the authority of Mr. Andrews, who discovered the plant, informed me that this monstrosity could be propagated by seed. With respect to the poppy see Prof. Goeppert as quoted in ‘Journal of Horticulture’ July 1, 1863 page 171.) Lastly, with respect to peloric flowers, which depart wonderfully from the natural structure,–those of Linaria vulgaris seem generally to be more or less sterile, whilst those before described of Antirrhinum majus, when artificially fertilised with their own pollen, are perfectly fertile, though sterile when left to themselves, for bees are unable to crawl into the narrow tubular flower. The peloric flowers of Corydalis solida, according to Godron (18/95. ‘Comptes Rendus’ December 19, 1864 page 1039.), are sometimes barren and sometimes fertile; whilst those of Gloxinia are well known to yield plenty of seed. In our greenhouse Pelargoniums, the central flower of the truss is often peloric, and Mr. Masters informs me that he tried in vain during several years to get seed from these flowers. I likewise made many vain attempts, but sometimes succeeded in fertilising them with pollen from a normal flower of another variety; and conversely I several times fertilised ordinary flowers with peloric pollen. Only once I succeeded in raising a plant from a peloric flower fertilised by pollen from a peloric flower borne by another variety; but the plant, it may be added, presented nothing particular in its structure. Hence we may conclude that no general rule can be laid down; but any great deviation from the normal structure, even when the reproductive organs themselves are not seriously affected, certainly often leads to sexual impotence.
DOUBLE FLOWERS. — When the stamens are converted into petals, the plant becomes on the male side sterile; when both stamens and pistils are thus changed, the plant becomes completely barren. Symmetrical flowers having numerous stamens and petals are the most liable to become double, as perhaps follows from all multiple organs being the most subject to variability. But flowers furnished with only a few stamens, and others which are asymmetrical in structure, sometimes become double, as we see with the double gorse or Ulex, and Antirrhinum. The Compositae bear what are called double flowers by the abnormal development of the corolla of their central florets. Doubleness is sometimes connected with prolification (18/96. ‘Gardener’s Chronicle’ 1866 page 681.), or the continued growth of the axis of the flower. Doubleness is strongly inherited. No one has produced, as Lindley remarks (18/97. ‘Theory of Horticulture’ page 333.), double flowers by promoting the perfect health of the plant. On the contrary, unnatural conditions of life favour their production. There is some reason to believe that seeds kept during many years, and seeds believed to be imperfectly fertilised, yield double flowers more freely than fresh and perfectly fertilised seed. (18/98. Mr. Fairweather ‘Transact. Hort. Soc.’ volume 3 page 406: Bosse quoted by Bronn ‘Geschichte der Natur’ b. 2 s. 77. On the effects of the removal of the anthers see Mr. Leitner in Silliman’s ‘North American Journ. of Science’ volume 23 page 47; and Verlot ‘Des Varietes’ 1865 page 84.) Long-continued cultivation in rich soil seems to be the commonest exciting cause. A double narcissus and a double Anthemis nobilis, transplanted into very poor soil, has been observed to become single (18/99. Lindley’s ‘Theory of Horticulture’ page 3?3.); and I have seen a completely double white primrose rendered permanently single by being divided and transplanted whilst in full flower. It has been observed by Professor E. Morren that doubleness of the flowers and variegation of the leaves are antagonistic states; but so many exceptions to the rule have lately been recorded (18/100. ‘Gardener’s Chronicle’ 1865 page 626; 1866 pages 290, 730; and Verlot ‘Des Varietes’ page 75.), that, though general, it cannot be looked at as invariable. Variegation seems generally to result from a feeble or atrophied condition of the plant, and a large proportion of the seedlings raised from parents, if both are variegated, usually perish at an early age; hence we may perhaps infer that doubleness, which is the antagonistic state, commonly arises from a plethoric condition. On the other hand, extremely poor soil sometimes, though rarely, appears to cause doubleness: I formerly described (18/101. ‘Gardener’s Chronicle’ 1843 page 628. In this article I suggested the theory above given on the doubleness of flowers. This view is adopted by Carriere ‘Production et Fix. des Varietes’ 1865 page 67.) some completely double, bud-like, flowers produced in large numbers by stunted wild plants of Gentiana amarella growing on a poor chalky bank. I have also noticed a distinct tendency to doubleness in the flowers of a Ranunculus, Horse-chestnut, and Bladder-nut (Ranunculus repens, Aesculus pavia, and Staphylea), growing under very unfavourable conditions. Professor Lehmann (18/102. Quoted by Gartner ‘Bastarderzeugung’ s. 567.) found several wild plants growing near a hot spring with double flowers. With respect to the cause of doubleness, which arises, as we see, under widely different circumstances, I shall presently attempt to show that the most probable view is that unnatural conditions first give a tendency to sterility, and that then, on the principle of compensation, as the reproductive organs do not perform their proper functions, they either become developed into petals, or additional petals are formed. This view has lately been supported by Mr. Laxton (18/103. ‘Gardener’s Chronicle’ 1866 page 901.) who advances the case of some common peas, which, after long-continued heavy rain, flowered a second time, and produced double flowers.
SEEDLESS FRUIT. — Many of our most valuable fruits, although consisting in a homological sense of widely different organs, are either quite sterile, or produce extremely few seeds. This is notoriously the case with our best pears, grapes, and figs, with the pine-apple, banana, bread-fruit, pomegranate, azarole, date-palms, and some members of the orange-tribe. Poorer varieties of these same fruits either habitually or occasionally yield seed. (18/104. Lindley ‘Theory of Horticulture’ pages 175-179; Godron ‘De l’Espece’ tome 2 page 106; Pickering ‘Races of Man;’ Gallesio ‘Teoria della Riproduzione’ l816 pages 101-110. Meyen ‘Reise um Erde’ Th. 2 s. 214 states that at Manilla one variety of the banana is full of seeds: and Chamisso (Hooker’s ‘Bot. Misc.’ volume 1 page 310) describes a variety of the bread-fruit in the Mariana Islands with small fruit, containing seeds which are frequently perfect. Burnes in his ‘Travels in Bokhara’ remarks on the pomegranate seeding in Mazenderan, as a remarkable peculiarity.) Most horticulturists look at the great size and anomalous development of the fruit as the cause, and sterility as the result; but the opposite view, as we shall presently see, is more probable.
STERILITY FROM THE EXCESSIVE DEVELOPMENT OF THE ORGANS OF GROWTH OR VEGETATION. — Plants which from any cause grow too luxuriantly, and produce leaves, stems, runners, suckers, tubers, bulbs, etc., in excess, sometimes do not flower, or if they flower do not yield seed. To make European vegetables under the hot climate of India yield seed, it is necessary to check their growth; and, when one-third grown, they are taken up, and their stems and tap-roots are cut or mutilated. (18/105. Ingledew in ‘Transact. of Agricult. and Hort. Soc. of India’ volume 2.) So it is with hybrids; for instance, Prof. Lecoq (18/106. ‘De la Fecondation’ 1862 page 308.) had three plants of Mirabilis, which, though they grew luxuriantly and flowered, were quite sterile; but after beating one with a stick until a few branches alone were left, these at once yielded good seed. The sugar-cane, which grows vigorously and produces a large supply of succulent stems, never, according to various observers, bears seed in the West Indies, Malaga, India, Cochin China, Mauritius, or the Malay Archipelago. (18/107. Hooker ‘Bot. Misc.’ volume 1 page 99; Gallesio ‘Teoria della Riproduzione’ page 110. Dr. J. de Cordemoy in ‘Transact. of the R. Soc. of Mauritius’ new series volume 6 1873 pages 60-67, gives a large number of cases of plants which never seed, including several species indigenous in Mauritius.) Plants which produce a large number of tubers are apt to be sterile, as occurs, to a certain extent, with the common potato; and Mr. Fortune informs me that the sweet potato (Convolvulus batatas) in China never, as far as he has seen, yields seed. Dr. Royle remarks (18/108. ‘Transact. Linn. Soc.’ volume 17 page 563.) that in India the Agave vivipara, when grown in rich soil, invariably produces bulbs, but no seeds; whilst a poor soil and dry climate lead to an opposite result. In China, according to Mr. Fortune, an extraordinary number of little bulbs are developed in the axils of the leaves of the yam, and this plant does not bear seed. Whether in these cases, as in those of double flowers and seedless fruit, sexual sterility from changed conditions of life is the primary cause which leads to the excessive development of the organs of vegetation, is doubtful; though some evidence might be advanced in favour of this view. It is perhaps a more probable view that plants which propagate themselves largely by one method, namely by buds, have not sufficient vital power or organised matter for the other method of sexual generation.
Several distinguished botanists and good practical judges believe that long- continued propagation by cuttings, runners, tubers, bulbs, etc., independently