The connection between the seeding of plants and their natural death has been recognised for long, and is usually explained as being due to the exhaustion of the plant.

As I am not a botanist, and was anxious to know the views of botanists on natural death, I wrote to Prof. de Vries, as a universally accepted authority. The distinguished botanist replied to me as follows. “Your question is extremely difficult. I do not think that much is known as to the exact cause of the death of annual plants, but it is customary to attribute it to exhaustion.” All the botanists who have expressed opinions on this matter appear to hold a similar view. Hildebrand,[81] the author of a memoir on the duration of life in plants, stated this view again and again. According to him “the life of annuals is usually short because they are exhausted by their extensive production of seeds (p. 116).” “Even amongst plants which produce seeds for several years, there are some which are prematurely exhausted by fructification and which die spontaneously” (p. 67). In the prothallus of many of the higher cryptogams, the formation of a single embryo is followed by natural death; as Goebel[82] points out, the embryo completely absorbs the prothallus.

As plants generally obtain their food with ease, it is natural to ask what is the cause of the exhaustion after seeding. When a plant which cannot resist cold dies after it has produced its seeds in the end of the summer, the event is natural enough. But how can we explain the death of an annual plant which is growing in a rich soil, and which seeds in the beginning of the summer, as being due to exhaustion long before the winter cold. It frequently happens that after harvest new shoots spring up from grains which have fallen. The soil which can support this new vegetation cannot have been exhausted by the cereal in question; and there has been enough warmth for the new crop. It cannot be the external conditions which have caused the death of the parent plant. The explanation of this apparent contradiction has been sought in the constitution of the plant itself. Hildebrand remarks that “certain species have a constitution which tends to early fructification. As soon as the seeds have been set, the strength of the plant is exhausted in the swelling of the grains, so that the plant dies.” “Other species, on the contrary, are so constituted that they vegetate for a long time, before fruiting, after which, however, they also die. A third set of plants have such a constitution that “they do not die after seeding, that they can seed often and live for many years” (p. 113).

Being unable to indicate exactly the intrinsic mechanism of these different “constitutions,” several botanists explain them by a kind of teleological predestination. According to Hildebrand “the nutritive processes of a plant have no other purpose than to make it capable of reproduction; this final end, however, can be reached in different modes and after different periods of time” (p. 132). Goebel sets down similar views. “In heterosporous plants the whole course of the development of prothalli is predetermined. The prothalli, so far as we actually know, to use the phrase of theologians, are predestined; their fate is determined once for all” (p. 403). M. Massart[83] expresses the same kind of view, when he says that “sometimes cells die because their work is finished, and they have no longer any reason for existing.”

Such an interpretation of the facts is quite opposed to determinism, and makes the problem of natural death in the plant world more difficult but more interesting.

The modern scientific conception of the universe excludes the idea of predestination. The relations between fructification and natural death must be regulated by the law of selection, according to which no organism survives if its reproduction is impossible. It occasionally happens that children are born without organs which are indispensable to life. Such monsters of different kinds being non-viable, cannot be said to be predestined to death, as they die because of defects in their structure. Others are born with all that is necessary for life, and survive for that reason, not because they are predestined to life. So also species of plants which develop incompletely and which die before they have produced spores or seeds, cannot survive; whilst those which die after having given birth to the next generation survive in their descendants. However quickly death follow the production of seed, the species will survive equally well. The cause of the natural death of plants must be sought, therefore, not in predestination, but in the mechanism of the organic processes.

Nothing seems more probable than that a plant should die when all its organic forces have been exhausted. It would be interesting, however, to ascertain the mechanism of that exhaustion, and this especially because it is often very difficult to imagine a cause for it. Many plants exist which produce several generations each season, in the same soil, without exhausting it. In perennial plants, some parts, such as the flowers, die periodically, although the plant itself is not exhausted. Everyone has seen that in geraniums some of the flowers wither whilst others are blooming, the process going on throughout the season. We can scarcely attribute such a natural death of the flowers to any exhaustion of the plant which continues to produce new flowers.

The fairly frequent prolongation of the life of plants is also out of harmony with the theory of natural death as the result of exhaustion. It sometimes happens that male plants produce female flowers abnormally; cases of this kind have been observed in willows, stinging-nettles, hops, and especially in maize.[84] Here we have to deal with a kind of monstrosity, differing, however, from the non-viable monsters of the human race, in the respect that the production of female flowers on the male branches results in the prolongation of their lives. Generally the male branches die a natural death as soon as the pollen has been shed, and therefore some time before the death of the female flowers. If, however, a male branch bears a female flower which becomes fertilised, then the life of the branch is prolonged until the seeds ripen. If the natural death of the male flowers is the result of exhaustion due to the development of the pollen, how can we reconcile this with the prolongation of life in a case where the male branch has also female flowers to nourish and seeds to mature?

It is quite clear that natural death, in such cases, is the result of a mechanism more complex than simple exhaustion.

Prof. de Vries has already noted that the duration of life in plants depends on their vital processes. That view implies that there are some qualities inherent in its organisation which can prolong or shorten the life of a plant, and it is here that we ought to find the key to the problem of natural death in the vegetable world. However, to gain exact knowledge of such factors, it would be necessary to have information on many points in plant physiology which unfortunately are very imperfectly known. In this respect, the vital conditions of the simplest plants, such as yeasts and bacteria, have been investigated much more fully. It is true that such low organisms reproduce freely either by division or by budding, so that they are amongst the organisms in which natural death is not inevitable. None the less, in their lives phenomena occasionally present themselves which can be interpreted as cases of natural death.