The principal kinds of cabbage existed at least as early as the sixteenth century,[[70]] so that numerous modifications of structure have been inherited for a long period. This fact is the more remarkable as great care must be taken to prevent the crossing of the different kinds. To give proof of this: I raised 233 seedlings from cabbages of different kinds, which had purposely been planted near each other, and of the seedlings no less than 155 were plainly deteriorated and mongrelised; nor were the remaining 78 all perfectly true. It may be doubted whether many permanent varieties have been formed by intentional or accidental crosses; for such crossed plants are found to be very inconstant. One kind, however, called “Cottager’s Kail,” has lately been produced by crossing common kail and Brussel-sprouts, recrossed with purple broccoli,[[71]] and is said to be true; but plants raised by me were not nearly so constant in character as any common kind of cabbage.
Although most of the kinds keep true if carefully preserved from crossing, yet the seed-beds must be yearly examined, and a few seedlings are generally found false; but even in this case the force of inheritance is shown, for, as Metzger has remarked[[72]] when speaking of Brussel-sprouts, the variations generally keep to their “unter art,” or main race. But in order that any kind may be truly propagated there must be no great change in the conditions of life; thus cabbages will not form heads in hot countries, and the same thing has been observed with an English variety grown during an extremely warm and damp autumn near Paris.[[73]] Extremely poor soil also affects the characters of certain varieties.
Most authors believe that all the races are descended from the wild cabbage found on the western shores of Europe; but Alph. De Candolle[[74]] forcibly argues, on historical and other grounds, that it is more probable that two or three closely allied forms, generally ranked as distinct species, still living in the Mediterranean region, are the parents, now all commingled together, of the various cultivated kinds. In the same manner as we have often seen with domesticated animals, the supposed multiple origin of the cabbage throws no light on the characteristic differences between the cultivated forms. If our cabbages are the descendants of three or four distinct species, every trace of any sterility which may originally have existed between them is now lost, for none of the varieties can be kept distinct without scrupulous care to prevent intercrossing.
The other cultivated forms of the genus Brassica are descended, according to the view adopted by Godron and Metzger,[[75]] from two species, B. napus and rapa; but according to other botanists from three species; whilst others again strongly suspect that all these forms, both wild and cultivated, ought to be ranked as a single species. Brassica napus has given rise to two large groups, namely, Swedish turnips (believed to be of hybrid origin)[[76]] and Colzas, the seeds of which yield oil. Brassica rapa (of Koch) has also given rise to two races, namely, common turnips and the oil-giving rape. The evidence is unusually clear that these latter plants, though so different in external appearance, belong to the same species; for the turnip has been observed by Koch and Godron to lose its thick roots in uncultivated soil; and when rape and turnips are sown together they cross to such a degree that scarcely a single plant comes true.[[77]] Metzger by culture converted the biennial or winter rape into the annual or summer rape,—varieties which have been thought by some authors to be specifically distinct.[[78]]
In the production of large, fleshy, turnip-like stems, we have a case of analogous variation in three forms which are generally considered as distinct species. But scarcely any modification seems so easily acquired as a succulent enlargement of the stem or root—that is, a store of nutriment laid up for the plant’s own future use. We see this in our radishes, beet, and in the less generally known “turnip-rooted” celery, and in the finocchio, or Italian variety of the common fennel. Mr. Buckman has lately proved by his interesting experiments bow quickly the roots of the wild parsnip can be enlarged, as Vilmorin formerly proved in the case of the carrot.[[79]]
This latter plant, in its cultivated state, differs in scarcely any character from the wild English carrot, except in general luxuriance and in the size and quality of its roots; but ten varieties, differing in the colour, shape, and quality of the root, are cultivated in England and come true by seed.[[80]] Hence with the carrot, as in so many other cases, for instance with the numerous varieties and sub-varieties of the radish, that part of the plant which is valued by man, falsely appears alone to have varied. The truth is that variations in this part alone have been selected; and the seedlings inheriting a tendency to vary in the same way, analogous modifications have been again and again selected, until at last a great amount of change has been effected.
With respect to the radish, M. Carrière, by sowing the seed of the wild Raphanus raphanistrum in rich soil, and by continued selection during several generations, raised many varieties, closely like the cultivated radish (R. sativus) in their roots, as well as the wonderful Chinese variety, R. caudatus: (see ‘Journal d’Agriculture pratique,’ tom. i, 1869, p. 159; also a separate essay ‘Origine des Plantes Domestiques,’ 1869.) Raphanus raphanistrum and sativus have often been ranked as distinct species, and owing to differences in their fruit even as distinct genera; but Professor Hoffman (‘Bot. Zeitung,’ 1872, p. 482) has now shown that these differences, remarkable as they are, graduate away, the fruit of R. caudatus being intermediate. By cultivating R. raphanistrum during several generations (ibid., 1873, p. 9), Professor Hoffman also obtained plants bearing fruits like those of R. sativus.
Pea (Pisum sativum).—Most botanists look at the garden-pea as specifically distinct from the field-pea (P. arvense). The latter exists in a wild state in Southern Europe; but the aboriginal parent of the garden-pea has been found by one collector alone, as he states, in the Crimea.[[81]] Andrew Knight crossed, as I am informed by the Rev. A. Fitch, the field-pea with a well-known garden variety, the Prussian pea, and the cross seems to have been perfectly fertile. Dr. Alefield has recently studied[[82]] the genus with care, and, after having cultivated about fifty varieties, concludes that certainly they all belong to the same species. It is an interesting fact already alluded to, that, according to O. Heer,[[83]] the peas found in the lake-habitations of Switzerland of the Stone and Bronze ages, belong to an extinct variety, with exceedingly small seeds, allied to P. arvense or the field-pea. The varieties of the common garden-pea are numerous, and differ considerably from one another. For comparison I planted at the same time forty-one, English and French varieties. They differed greatly in height,— namely from between 6 and 12 inches to 8 feet,[[84]]—in manner of growth, and in period of maturity. Some differ in general aspect even while only two or three inches in height. The stems of the Prussian pea are much branched. The tall kinds have larger leaves than the dwarf kinds, but not in strict proportion to their height:—Hair’s Dwarf Monmouth has very large leaves, and the Pois nain hatif, and the moderately tall Blue Prussian, have leaves about two-thirds of the size of the tallest kind. In the Danecroft the leaflets are rather small and a little pointed; in the Queen of Dwarfs rather rounded; and in the Queen of England broad and large. In these three peas the slight differences in the shape of the leaves are accompanied by slight differences in colour, in the Pois géant sans parchemin, which bears purple flowers, the leaflets in the young plant are edged with red; and in all the peas with purple flowers the stipules are marked with red.
In the different varieties, one, two, or several flowers in a small cluster, are borne on the same peduncle; and this is a difference which is considered of specific value in some of the Leguminosæ. In all the varieties the flowers closely resemble each other except in colour and size. They are generally white, sometimes purple, but the colour is inconstant even in the same variety. In Warner’s Emperor, which is a tall kind, the flowers are nearly double the size of the Pois nain hatif; but Hair’s Dwarf Monmouth, which has large leaves, likewise has large flowers. The calyx in the Victoria Marrow is large, and in Bishop’s Long Pod the sepals are rather narrow. In no other kind is there any difference in the flower.
The pods and seeds, which with natural species afford such constant characters, differ greatly in the cultivated varieties of the pea; and these are the valuable, and consequently the selected parts. Sugar peas, or P, are remarkable from their thin pods, which, whilst young, are cooked and eaten whole; and in this group, which, according to Mr. Gordon includes eleven sub-varieties, it is the pod which differs most; thus Lewis’s Negro-podded pea has a straight, broad, smooth, and dark-purple pod, with the husk not so thin as in the other kinds; the pod of another variety is extremely bowed; that of the Pois géant is much pointed at the extremity; and in the variety “à grands cosses” the peas are seen through the husk in so conspicuous a manner that the pod, especially when dry, can hardly at first be recognised as that of a pea.