Гаметофит и спорофит в жизненном цикле растений и водорослей.

Haploid stage in the life cycle of plants and algae

A gametophyte (/g//ə/'/m//iː//t//ə//f//aɪ//t/) is one of the two alternating multicellular phases in the life cycles of plants and algae. It is a haploid multicellular organism that develops from a haploid spore that has one set of chromosomes. The gametophyte is the sexual phase in the life cycle of plants and algae. It develops sex organs that produce gametes, haploid sex cells that participate in fertilization to form a diploid zygote which has a double set of chromosomes. Cell division of the zygote results in a new diploid multicellular organism, the second stage in the life cycle known as the sporophyte. The sporophyte can produce haploid spores by meiosis that on germination produce a new generation of gametophytes.

In some multicellular green algae (Ulva lactuca is one example), red algae and brown algae, sporophytes and gametophytes may be externally indistinguishable (isomorphic). In Ulva the gametes are isogamous, all of one size, shape and general morphology.

In land plants, anisogamy is universal. As in animals, female and male gametes are called, respectively, eggs and sperm. In extant land plants, either the sporophyte or the gametophyte may be reduced (heteromorphic). No extant gametophytes have stomata, but they have been found on fossil species like the early Devonian Aglaophyton from the Rhynie chert. Other fossil gametophytes found in the Rhynie chert shows they were much more developed than present forms, resembling the sporophyte in having a well developed conducting strand, a cortex, an epidermis and a cuticle with stomata, but were much smaller.

In bryophytes (mosses, liverworts, and hornworts), the gametophyte is the most visible stage of the life cycle. The bryophyte gametophyte is longer lived, nutritionally independent, and the sporophytes are attached to the gametophytes and dependent on them. When a moss spore germinates it grows to produce a filament of cells (called the protonema). The mature gametophyte of mosses develops into leafy shoots that produce sex organs (gametangia) that produce gametes. Eggs develop in archegonia and sperm in antheridia. In some bryophyte groups such as many liverworts of the order Marchantiales, the gametes are produced on specialized structures called gametophores (or gametangiophores).

All vascular plants are sporophyte dominant, and a trend toward smaller and more sporophyte dependent female gametophytes is evident as land plants evolved reproduction by seeds. Those vascular plants, such as clubmosses and many ferns, that produce only one type of spore are said to be homosporous. They have exosporic gametophytes — that is, the gametophyte is free living and develops outside of the spore wall. Exosporic gametophytes can either be bisexual, capable of producing both sperm and eggs in the same thallus (monoicous), or specialized into separate male and female organisms (dioicous). In heterosporous vascular plants (plants that produce both microspores and megaspores), the gametophytes develop endosporically (within the spore wall). These gametophytes are dioicous, producing either sperm or eggs but not both.

In most ferns, for example, in the leptosporangiate fern Dryopteris, the gametophyte is a photosynthetic free living autotrophic organism called a prothallus that produces gametes and maintains the sporophyte during its early multicellular development. However, in some groups, notably the clade that includes Ophioglossaceae and Psilotaceae, the gametophytes are subterranean and subsist by forming mycotrophic relationships with fungi. Homosporous ferns secrete a chemical called antheridiogen.

Extant lycophytes produce two different types of gametophytes. In the homosporous families Lycopodiaceae and Huperziaceae, spores germinate into bisexual free living, subterranean and mycotrophic gametophytes that derive nutrients from symbiosis with fungi. In Isoetes and Selaginella, which are heterosporous, microspores and megaspores are dispersed from sporangia either passively or by active ejection. Microspores produce microgametophytes which produce sperm. Megaspores produce reduced megagametophytes inside the spore wall. At maturity, the megaspore cracks open at the trilete suture to allow the male gametes to access the egg cells in the archegonia inside. The gametophytes of Isoetes appear to be similar in this respect to those of the extinct Carboniferous arborescent lycophytes Lepidodendron and Lepidostrobus.

The seed plant gametophyte life cycle is even more reduced than in basal taxa (ferns and lycophytes). Seed plant gametophytes are not independent organisms and depend upon the dominant sporophyte tissue for nutrients and water. With the exception of mature pollen, if the gametophyte tissue is separated from the sporophyte tissue it will not survive. Due to this complex relationship and the small size of the gametophyte tissue—in some situations single celled—differentiating with the human eye or even a microscope between seed plant gametophyte tissue and sporophyte tissue can be a challenge. While seed plant gametophyte tissue is typically composed of mononucleate haploid cells (1 x n), specific circumstances can occur in which the ploidy does vary widely despite still being considered part of the gametophyte. In gymnosperms, the male gametophytes are produced inside microspores within the microsporangia located inside male cones or microstrobili. In each microspore, a single gametophyte is produced, consisting of four haploid cells produced by meiotic division of a diploid microspore mother cell. At maturity, each microspore derived gametophyte becomes a pollen grain. During its development, the water and nutrients that the male gametophyte requires are provided by the sporophyte tissue until they are released for pollination. The cell number of each mature pollen grain varies between the gymnosperm orders. Cycadophyta have 3 celled pollen grains while Ginkgophyta have 4 celled pollen grains. The megastrobilus sporophytic tissue provides nutrients for the male gametophyte at this stage. After fertilization is complete in all orders, the remaining male gametophyte tissue will deteriorate. Similar to the male gametophyte, the female gametophyte normally is fully dependent on the surrounding sporophytic tissue for nutrients and the two organisms cannot be separated. However, the female gametophytes of Ginkgo biloba do contain chlorophyll and can produce some of their own energy, though, not enough to support itself without being supplemented by the sporophyte. The female gametophyte forms from a diploid megaspore that undergoes meiosis and starts being singled celled. The size of the mature female gametophyte varies drastically between gymnosperm orders. In Cycadophyta, Ginkgophyta, Coniferophyta, and some Gnetophyta, the single celled female gametophyte undergoes many cycles of mitosis ending up consisting of thousands of cells once mature. At a minimum, two of these cells are egg cells and the rest are haploid somatic cells, but more egg cells may be present and their ploidy, though typically haploid, may vary. In select Gnetophyta, the female gametophyte stays singled celled. Mitosis does occur, but no cell divisions are ever made. One cell is the tube cell, and the remaining cell/cells are the sperm cells. The development of the three celled male gametophyte prior to dehiscing has evolved multiple times and is present in about a third of angiosperm species allowing for faster fertilization after pollination. Once pollination occurs, the tube cell grows in size and if the male gametophyte is only 2 cells at this stage, the single sperm cell undergoes mitosis to create a second sperm cell. Just like in gymnosperms, the tube cell in angiosperms obtains nutrients from the sporophytic tissue, and may branch out into the pistil tissue or grow directly towards the ovule. Once double fertilization is completed, the tube cell and other vegetative cells, if present, are all that remains of the male gametophyte and soon degrade. In general, it will then divide by mitosis until it consists of 8 nuclei separated into 1 egg cell, 3 antipodal cells, 2 synergid cells, and a central cell that contains two nuclei. Conversely, some species have 10 celled mature female gametophytes consisting of 16 total nuclei. Once double fertilization occurs, the egg cell becomes the zygote which is then considered sporophyte tissue. Scholars still disagree on whether the fertilized central cell is considered gametophyte tissue. Some botanists consider this endospore as gametophyte tissue with typically 2/3 being female and 1/3 being male, but as the central cell before double fertilization can range from 1n to 8n in special cases, the fertilized central cells range from 2n (50% male/female) to 9n (1/9 male, 8/9th female). In angiosperms, the megagametophyte is reduced to only a few cells, and is sometimes called the embryo sac. A typical embryo sac contains seven cells and eight nuclei, one of which is the egg cell. Two nuclei fuse with a sperm nucleus to form the primary endospermic nucleus which develops to form triploid endosperm, which becomes the food storage tissue in the seed.