After separation the bud is nourished either by the new plant on which it has been grafted, or by means of the roots which it forms immediately when planted in the soil.

90

The eye consists of nodes and leaves in a more or less developed condition, destined to enlarge and expand the growing plant.

In effect, the side twigs which sprout from the nodes may be regarded as distinct little plants, growing on the parent plant just as the latter grows in the earth.

91

The comparison of seed and eye has so often been made, and especially quite recently, with such penetration and exactitude, that we can but appeal to this work with unqualified approbation.

92

We will only state the following: In highly organised plants nature makes a clear difference between eyes and seeds. In more simply formed plants, however, this difference no longer seems apparent, even to the most acute observer. There are seeds which are undoubtedly seeds, and eyes which are undoubtedly eyes, but it is only possible to conceive, and not in any outward way to see, where the line of demarcation lies between properly fertilised seeds, separated from the parent plant by the reproductive process, and propagative buds which simply push their way out from the parent plant and separate from it without any apparent cause.

93

Having weighed this well in our minds we may venture to think that seeds, though they differ from eyes by being completely enclosed, and from propagative buds by the visible cause of their formation and separation from the parent plant, are yet closely related to both.

CHAPTER XIV

FORMATION OF COMPOSITE FLOWERS AND FRUITS

94

We have so far tried to explain by the transformation of the stem-leaves, the formation of single flowers and also seeds produced within a closed capsule. Closer examination will show that in these instances no eyes are developed; indeed there is absolutely no possibility for such a development to take place. To understand the composite flower however, as well as the compound fruit gathered around a single cone, spindle, dies or the like, we must look to the development of eyes.

95

We often see that stems, without preparing long beforehand or reserving their energy for the development of a single flower, bring forth blossoms already at their nodes, often continuing in this way uninterruptedly to the very tip. This may be explained however by the theory already propounded. All flowers developed from eyes may be regarded as distinct plants growing on the parent plant, just as the parent plant grows on the earth. Supplied, however, as they are with purer juices by the nodes, even the first leaves of the little twigs are much more finely formed than the first leaves of the parent plant which came after the cotyledons; indeed, even the immediate formation of calyx and flower is often possible.

96

Even these blossoms that develop out of eyes, had they received more copious nourishment, would have become twigs and have undergone a destiny similar to that of the parent plant.

97

During the development of such flowers from node to node, we notice too that same transformation of the stem-leaves which we observed when the transition to the calyx took place slowly. The leaves contract more and more, until at last they almost disappear. They are then called bracts, and have more or less lost their leaf-like form. Just in the same proportion as the stem becomes thinner, so do the nodes move closer together, and everything that happened in the transition to the calyx happens now, except that no particular terminal flower appears at the tip, because Nature has already fulfilled her task at each successive eye.

98

Now when we have contemplated well such a stem adorned at each node with a blossom, we shall more easily understand a composite flower, especially if we remember what has already been said about the origin of the calyx.

99

Nature forms a composite calyx, (involucre) from a number of leaves by pressing them close to one another and arranging them around an axis. With this same strong impulse of growth she develops, so to speak, one infinite stem, producing all its eyes at the same time and as near together as possible in the form of a flower, each separate floret fructifying the seed-vessel already prepared below it. Nor are the nodal leaves always entirely lost in this tremendous contraction. In thistles for example (compare Dipsacus laciniatus), the little leaf faithfully accompanies the floret which grows from the eye situated close by it. In many grasses, too, each flower has such a leaflet, which in this case is called a glume.

100

So we are led to see that the seeds of a composite flower are true eyes, formed and developed by means of the male and female organs. We shall easily be convinced that this is so if, keeping this idea always in mind, we examine and compare the growth and manner of seeding of various plants.

101

Then, too, we shall not find it difficult to explain the seeds—whether enclosed within a seed-vessel or not—which are produced in the middle of a single flower. For it comes to the same thing if a single flower surrounds a compound ovary, whose united pistils suck in the fertilising juices from the anthers and pass them on to the ovules, or if each ovule has its own pistil, and anthers and petals.

102

We are convinced that with a little practice it would not be difficult to explain in this way the manifold forms of flowers and fruits. But it would of course require complete familiarity with the above stated ideas of expansion and contraction, approximation and anastomosis, to be able to apply them in their right place as one would use algebraic formulae. And as much depends on the exact observation and comparison of the various stages through which Nature passes, both in the forming of genera, species and varieties, and in the growth of each individual plant, a collection of illustrations made for this purpose with explanations of the different parts of the plant in botanical terminology would be both welcome and useful. Two strange instances of proliferous flowers, if we could have them before us, would help most decidedly in upholding this theory.

CHAPTER XV

A PROLIFEROUS ROSE

103

All that we have been seeking to grasp by powers of imagination and thought is shown most clearly in the instance of the proliferous rose. The calyx and corolla are arranged and developed around the axis; but instead of the seed-vessel contracted in the centre of the blossom, with the masculine and feminine organs arranged around, the stem, half red and half green, continues upward, while from it arise in succession smaller, dark red, folded petals, some of them bearing traces of anthers. The stem goes on growing, thorns appear on it again, the coloured petals which now appear singly become smaller and at last transform into variegated stem-leaves, half red and half green; a series of regular nodes is formed and from their eyes small, though imperfect, rosebuds appear once more.

104

This example in particular affords visible proof of our theory, namely, that all calyces are simply leaves, folia floralia, contracted and growing together at the periphery. For in this specimen the calyx, gathered round the axis, consists of five perfectly developed, compound leaves of three or five leaflets, such as are normally produced by rose branches at their nodes.

CHAPTER XVI

A PROLIFEROUS CARNATION

105

Strange as this phenomenon will appear to us when we contemplate it, yet another—a proliferous carnation—is still more remarkable. We see a perfect flower with a calyx and a double corolla; in the centre is a seed-capsule, not, however, quite fully developed. From the sides of the corolla four new and perfect flowers are developed, separated from the parent-flower by stalks three or four nodes or more in length. These new flowers, too, have calyces and double corollas, formed not so much of single petals as of little crowns of petals united at their base, or more often of petals which have developed like little twigs and grown together round a stem. Notwithstanding this monstrous development, filaments and anthers are present in some of these flowers. Fruit capsules are there with their styles, the capsules appearing again in leaf-form. Indeed, in one flower the seed-vessels were united into a perfect calyx and contained the rudiments of another complete, double flower.

106

While the rose was like a half completed flower, from the centre of which the stem again shot upward, bearing stem-leaves as before, the carnation, with a well formed calyx and perfect corolla and a capsule situated properly in the centre, had developed eyes from among the surrounding petals, producing actual twigs and flowers. We see, then, from these two instances, that Nature normally terminates the period of growth in the blossom—adds it up, so to speak, to a sum-total, so that by thus checking the possibility of gradual and infinite growth, she may achieve her aim the more quickly through the forming of seeds.

CHAPTER XVII

LINNAEUS’S THEORY OF ANTICIPATION

107

If here and there I may have stumbled on a path which one of my predecessors, though attempting it under the guidance of his great teacher, describes as so fearful and dangerous; or if I have not quite succeeded in levelling it and clearing it of every obstacle for those who come after me, yet I still hope that this will not have been a fruitless undertaking.

108

At this point it will be right to consider the theory by which Linnaeus sought to explain these phenomena.