The common carnation is strongly proterandrous, and therefore depends to a large extent upon insects for fertilisation. I have seen only humble-bees visiting the flowers, but I dare say other insects likewise do so. It is notorious that if pure seed is desired, the greatest care is necessary to prevent the varieties which grow in the same garden from intercrossing. (4/10. ‘Gardeners’ Chronicle’ 1847 page 268.) The pollen is generally shed and lost before the two stigmas in the same flower diverge and are ready to be fertilised. I was therefore often forced to use for self-fertilisation pollen from the same plant instead of from the same flower. But on two occasions, when I attended to this point, I was not able to detect any marked difference in the number of seeds produced by these two forms of self-fertilisation.

Several single-flowered carnations were planted in good soil, and were all covered with a net. Eight flowers were crossed with pollen from a distinct plant and yielded six capsules, containing on an average 88.6 seeds, with a maximum in one of 112 seeds. Eight other flowers were self-fertilised in the manner above described, and yielded seven capsules containing on an average 82 seeds, with a maximum in one of 112 seeds. So that there was very little difference in the number of seeds produced by cross-fertilisation and self-fertilisation, namely, as 100 to 92. As these plants were covered by a net, they produced spontaneously only a few capsules containing any seeds, and these few may perhaps be attributed to the action of Thrips and other minute insects which haunt the flowers. A large majority of the spontaneously self-fertilised capsules produced by several plants contained no seeds, or only a single one. Excluding these latter capsules, I counted the seeds in eighteen of the finest ones, and these contained on an average 18 seeds. One of the plants was spontaneously self-fertile in a higher degree than any of the others. On another occasion a single covered-up plant produced spontaneously eighteen capsules, but only two of these contained any seed, namely 10 and 15.

CROSSED AND SELF-FERTILISED PLANTS OF THE FIRST GENERATION.

The many seeds obtained from the above crossed and artificially self-fertilised flowers were sown out of doors, and two large beds of seedlings, closely adjoining one another, thus raised. This was the first plant on which I experimented, and I had not then formed any regular scheme of operation. When the two lots were in full flower, I measured roughly a large number of plants but record only that the crossed were on an average fully 4 inches taller than the self-fertilised. Judging from subsequent measurements, we may assume that the crossed plants were about 28 inches, and the self-fertilised about 24 inches in height; and this will give us a ratio of 100 to 86. Out of a large number of plants, four of the crossed ones flowered before any one of the self-fertilised plants.

Thirty flowers on these crossed plants of the first generation were again crossed with pollen from a distinct plant of the same lot, and yielded twenty-nine capsules, containing on an average 55.62 seeds, with a maximum in one of 110 seeds.

Thirty flowers on the self-fertilised plants were again self-fertilised; eight of them with pollen from the same flower, and the remainder with pollen from another flower on the same plant; and these produced twenty-two capsules, containing on an average 35.95 seeds, with a maximum in one of sixty-one seeds. We thus see, judging by the number of seeds per capsule, that the crossed plants again crossed were more productive than the self-fertilised again self-fertilised, in the ratio of 100 to 65. Both the crossed and self-fertilised plants, from having grown much crowded in the two beds, produced less fine capsules and fewer seeds than did their parents.

CROSSED AND SELF-FERTILISED PLANTS OF THE SECOND GENERATION.

The crossed and self-fertilised seeds from the crossed and self-fertilised plants of the last generation were sown on opposite sides of two pots; but the seedlings were not thinned enough, so that both lots grew very irregularly, and most of the self-fertilised plants after a time died from being smothered. My measurements were, therefore, very incomplete. From the first the crossed seedlings appeared the finest, and when they were on an average, by estimation, 5 inches high, the self-fertilised plants were only 4 inches. In both pots the crossed plants flowered first. The two tallest flower-stems on the crossed plants in the two pots were 17 and 16 1/2 inches in height; and the two tallest flower-stems on the self-fertilised plants 10 1/2 and 9 inches; so that their heights were as 100 to 58. But this ratio, deduced from only two pairs, obviously is not in the least trustworthy, and would not have been given had it not been otherwise supported. I state in my notes that the crossed plants were very much more luxuriant than their opponents, and seemed to be twice as bulky. This latter estimate may be believed from the ascertained weights of the two lots in the next generation. Some flowers on these crossed plants were again crossed with pollen from another plant of the same lot, and some flowers on the self-fertilised plants again self-fertilised; and from the seeds thus obtained the plants of the next generation were raised.

CROSSED AND SELF-FERTILISED PLANTS OF THE THIRD GENERATION.

The seeds just alluded to were allowed to germinate on bare sand, and were planted in pairs on the opposite sides of four pots. When the seedlings were in full flower, the tallest stem on each plant was measured to the base of the calyx. The measurements are given in Table 4/46. In Pot 1 the crossed and self-fertilised plants flowered at the same time; but in the other three pots the crossed flowered first. These latter plants also continued flowering much later in the autumn than the self-fertilised.