The ovule is not enclosed in an ovary, and the usually solitary macrospore becomes filled with a prothallus, in the upper part of which are formed several rudimentary archegonia.
Ovules naked, rarely without carpellary leaves, usually borne on carpophylls, which assume various forms. The single megaspore enclosed in the nucellus is filled with tissue (prothallus) before fertilization, and contains two or more archegonia, consisting usually of a large egg-cell and a small neck, rarely of an egg-cell only and no neck (Gnetum and Welwitschia).
Microspore spherical or oval, with or without a bladder-like extension of the exine, containing a prothallus of two or more cells, one of which produces two non-motile or motile male cells.
The megaspore-nucleus divides repeatedly, and cells are produced from the peripheral region inwards, which eventually fill the sporecavity with a homogeneous tissue (prothallus); some of the superficial cells at the micropylar end of the megaspore increase in size and divide by a tangential wall into two, an upper cell which gives rise to the short two-celled neck of the archegonium, and a lower cell which develops into a large egg-cell.
The megaspore becomes filled with tissue (prothallus), and from some of the superficial cells archegonia are produced, usually three to five in number, but in rare cases ten to twenty or even sixty may be present.
In the genus Sequoia there may be as many as sixty archegonia (Arnoldi and Lawson) in one megaspore; these occur either separately or in some parts of the prothallus they may form groups as in the Cupressineae; they are scattered through the prothallus instead of being confined to the apical region as in the majority of conifers.
Similarly in the Araucarieae and in Widdringtonia the archegonia are numerous and scattered and often sunk in the prothallus tissue.
Cupressineae) or separated from one another by a few cells of the prothallus, each ovum being immediately surrounded by a layer of cells distinguished by their granular contents and large nuclei.
The genus Ephedra, with its prothallus and archegonia, which are similar to those of other Gymnosperms, may be safely regarded as the most primitive of the Gnetales.
In Welwitschia also the megaspore is filled with prothallus-tissue, but single egg-cells take the place of archegonia.
In certain species of Gnetum described by Karsten the megaspore contains a peripheral layer of protoplasm, in which scattered nuclei represent the female reproductive cells; in Gnetum Gnemon a similar state of things exists in the upper half of the megaspore, while the lower half agrees with the megaspore of Welwitschia in being full of prothallus-tissue, which serves merely as a reservoir of food.
The archegonia are separated from one another, as in Pinus, by some of the prothallus-tissue, and the cells next the egg-cells (tapetal layer) contribute food-material to their development.
17, C, z and z'); they then grow into long tubes or proembryos, which make their way towards the prothallus (C, z'), and eventually embryos are formed from the ends of the proembryo tubes.
The megaspore of Welwitschia is filled with a prothallus-tissue before fertilization, and some of the prothallus-cells function as egg-cells; these grow upwards as long tubes into the apical region of the nucellus, where they come into contact with the pollen-tubes.
Green organism is developed; this is the prothallus (gametophyte, sexual generation; fig.
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.
Further, several spores will be likely to germinate together owing to their elaters becoming entangled; a fact of some importance, since the antheridia and archegonia, though occurring sometimes on the same prothallus, are more often borne on separate individuals.
There is some reason to believe that the prothallus of Psilotum resmbles some Lycopodium prothalli, but conclusive evidence is wanting; that of Tmesipteris is unknown.
B, Prothallus bearing young sporophyte.
The spores, when liberated by the dehiscence of the sporangium, give rise to the prothallus, which is now, owing mainly to the investigations of Treub and Bruchmann, known in a number of tropical and temperate species.
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.
A comparison of these various types would appear to indicate that the primitive form of prothallus in the genus was radially symmetrical and contained chlorophyll.
The different forms of the prothallus found in E.
Selago give an idea of how the more extremely modified types could be derived from such a prothallus as that of L.
Cernuum and other forms with superficial green prothalli is attached to the prothallus by a small foot, and develops at first as a tuberous body (the protocorm) bearing rhizoids; this forms a number of simple leaves, and upon it the apex of the shoot arises later.
Its prothallus resembles that of L.
On germination the microspores give rise to a reduced prothallus, consisting of the small cell first cut off and a wall of cells enclosing two to four central ones; "from these latter the biciliate spermatozoids originate.
The megaspore becomes filled with the female prothallus, the formation of cell-walls commencing at the pointed end of the spore, where from the first the nuclei are more numerous, and later extending to the base.
Thus the position of the root in Selaginella is different from what obtains in the other Vascular Cryptogams. A point of interest in this heterosporous genus is that the formation of the prothallus may commence before the megaspore is liberated from the sporangium.
The prothallus of 0.
Those of Ophioglossum are cylindrical, while the dorsiventral prothallus of Botrychium bears the sexual organs on the upper surface.
The prothallus developed from the spore is green and in most cases dorsiventral, bearing the archegonia and antheridia on the under surface.
The dorsiventrality of the prothallus has been shown to depend mainly on the illumination, the filamentous form being retained in feeble light; a similar result is obtained when the prothalli are cultivated in water.
The reproduction of the prothallus by gemmae in species of Trichomanes, Vittaria and Monogramme is another interesting adaptation; the prothallus of Gymnogramme (From Strasburger's Lehrbuck der Bolanik.) FIG.
In some apogamous Ferns sporangia may occur on the prothallus and the vegetative organs of the sporophyte may also occur singly.
A, Prothallus viewed from the lower surface; ar, archegonia; an, antheridia; rh, rhizoids (much enlarged).
The spores produce a green prothallus of large size, the sexual organs of which hardly project from the surface.
The cotyledon and stem grow up vertically through the prothallus, the root turning downwards into the soil.
The prothallus and sexual organs may resemble those of the Polypodiaceae; in Aneimia and Mohria the prothallus, though flattened, is not bilaterally symmetrical, the growing point being on one side; a filamentous type of prothallus is known in Schizaea.
The structure of the prothallus and sexual organs will be evident from figs.
The microspores on germination produce a small, greatly reduced male prothallus bearing one or two antheridia which give rise to a number of spirally coiled, multiciliate spermatozoids.
This, though at first dependent on the prothallus, soon becomes independent.
Mg, Membrane of functional megaspore, which is filled by the prothallus, pr.
Upper part of seed, in longitudinal section; i, integument; mi, micropyle; n, remains of nucellus; p.c, pollen-chamber (containing pollen-grains), with its canal extending up to the micropyle; pr, part of prothallus; ar, archegonia.