The sporophyte is always highly organized both as regards form and structure.
(X 8.) The adaptations in the vegetative organs of the sporophyte are similar to those Flowering Plants.
The independent plant which is generally attached to the soil by hair-like structures is the sexual generation, the sporophyte is a stalked or sessile capsule which remains always attached to the gametophyte from which it derives the whole or part of its nourishment.
The sporophyte is the plant which is differentiated into stem, leaf and root, which show a wonderful variety 01 form; the internal structure also shows increased complexity and variety as compared with the other group of vascular plants, the Pteridophyta.
After fertilization the female cell, now called the oospore, divides and part of it develops into the embryo (new sporophyte), which remains dormant for a time still protected by the ovule which has developed to become the seed.
Morphological identity) between the differentiated tissues of an Anthocerotean sporogonium and those of the sporophyte in the higher plants.
Ferns, horse-tails, club mosses, &c., and Phanerogams or Flowering Plants) the main plant-body, that which we speak of in ordinary language as the plant, is called the sporophyte because it bears the asexual reproductive cells or spores.
The body of the sporophyte in the great majority of the vascular plants shows a considerable increase in complexity over that found in the gametophyte of Bryophytes.
The structure of the stomata of the sporophyte of vascular plants is fundamentally the same as that of the stomata on the sporogonium of the true mosses and of the liverwort A nihoceros.
It is confined to the sporophyte, which forms the, leafy plant in these groups, and is known as the vascular system.
In this, as in all morphological inquiries, two lines of investigation have to be followed, the phylogenetic and the ontogenetic. Beginning with its phylogeny, it appears, so far as present knowledge goes, that the differentiation of the shoot of the sporophyte into stem and leaf first occurred in the Pteridophyta; and, in accordance with the views of Bower (Origin of a Land..
Thus in the series Bryophyta, Pteridophyta, Phanerogamia, whilst the sporophyte presents progressive development, the gametophyte presents continuous reduction.
This evolution of the sporophyte is no doubt to be correlated with the great change in the external conditions of life.
There is no conclusive ground for regarding the action of this change as having been direct, it is more reasonable to regard it as indirect, having acted as a general stimulus to which the ever-increasing complexity of the sporophyte was the response.
Concerning the second question, the recent investigations of Buchner ascogenous hyphae with their asci represent the sporophyte since they are derived from the fertilized ascogonium.
The matter is complicated by the apogamous transition from gametophyte to sporophyte in the absence of the ascogonium; also by the fact that there are normally two fusions in the life-history as mentioned earlier.
The last-mentioned case has been regarded as representing an apogamous development of the sporophyte from the gametophyte comparable to the cases of apogamy described in Ferns.
From egg to spore-mother-cell is sporophyte; from spore-mother-cell to egg is gametophyte.
If the sporophyte generation is confined to the cystocarp, is the tetrasporiferous plant, as has been suggested, merely a potential gametophyte reproducing by a process analogous to the budformation of the Bryophyta?
..Bangiaceae - Eti Florideae Eugleneae Chi Iromonadinae Pleurococcaceae - Endosphaeraceae Volvocaceae hlorosphaeraceae ï¿½ CoNJuGA'rAE, Siphonales Tetrasporaceao Ulvaceae Confdyvaleb Characeae in the culminating stage of Fucus, where the oogonium is separated from the stalk-cell, so that unless it be contended that the Fucus is really a sporophyte which does not produce spores, and that the gametophyte is represented merely by the oogonium and antheridium, there is no semblance of alternation of generation in this case.
The complete life-history, with its regular alternation of gametophyte and sporophyte, is now known in all except a few rare genera of recent Pteridophyta, and will be described in connexion with the several groups.
In habit and mode of life of the prothallus these present striking differences, which may be correlated with the situations inhabited by the sporophyte, and are perhaps to be regarded as adaptations which have enabled the species to survive.
Some of the more striking adaptive modifications in the gametophyte and sporophyte, and certain effects of altered external conditions which have been ascertained experimentally, may be briefly mentioned.
Size.) leptophylla is perennial, the sporophyte being annually borne on it.
In some apogamous Ferns sporangia may occur on the prothallus and the vegetative organs of the sporophyte may also occur singly.
On this view the origin of the sporophyte is looked for in the gradual development of sterile tissue in the generation arising from the fertilized ovum, and a consequent postponement of spore-formation.
Although the antithetic theory is supported by many facts regarding the lifehistory and structure of the group of plants under consideration, it is quite possible that a stage in which the sporophyte was wholly dependent on the gametophyte may never have been passed through in their evolution.
Without entering further into the discussion of these alternative theories, for which the literature of the subject must be consulted, it may be pointed out that on the latter view the strobiloid forms of Pteridophyta would not necessarily be regarded as primitive relatively to the large-leaved forms, and also that the early stages of the origin of the sporophyte in the two cases may have proceeded on different lines.
When the young sporophyte first begins its independent lifewhen, that is, it exists in the form of the embryo in the seedits living substance has no power of utilizing the simple inorganic compounds spoken of.
The sporophyte may be considered to begin at the stage of nuclear association and end with the nuclear reduction in the basidium.
As is well known, the dividing nuclei of the cells of the sporophyte generation of the higher plants exhibit a double number of chromosomes, while the dividing nuclei of the cells of the gametophyte generation exhibit the single number.
Upon the evidence it would seem therefore that so far as Nemalion is concerned an alternation occurs comparable with that existing in the lower Bryophyta where the sporophyte is relatively small, being attached to and to some extent parasitic upon the gametophyte.
It has been held by some, however, that the first brood corresponds to the sporophyte generation of the higher plants, and that the rest of the cycle is the gametophyte generation.
Blackman, who also succeeded in showing that the nuclei of the sporophyte generation contain twice as many chromosomes as the nuclei of the gametophyte.
The point common to all Pteridophyta is that from the first the gametophyte is an independent organism, while the sporophyte, though in the first stages of its development it obtains nutriment from the prothallus, becomes physiologically independent when its root develops.
On the one hand from the Bryophyta (in which the sporophyte is throughout its life attached to the gametophyte), and on the other hand from the Gymnosperms and Angiosperms (in which the more or less reduced gametophyte remains enclosed within the tissues of the sporophyte).
The early segmentation of the embryo differs in the several groups, but usually the first leaf or leaves, the apex of the stem and the first root are differentiated early, while a special absorbent organ (the foot) maintains for some time the physiological connexion between the sporophyte and the prothallus.
The main existing groups of the Filicaceae may now be briefly described, with special reference to the characters of gametophyte and sporophyte, which have been found of value in determining affinities.
The series which can be constructed from a study of the sorus is in general supported by the anatomy of the sporophyte, and by the structure and sexual organs of the gametophyte.
This surface layer in the typically subaerial shoot of the sporophyte in Pteridophytes and Phanerogams is known as the epidermis, though the name is restricted by some writers, on account of developmental differences, to the surface layer of the shoot of Angiosperms, and by others extended to the surface layer of the whole plant in both these groups.