Anther and Ovule Development in Tasmannia (Winteraceae)

1992 ◽  
Vol 40 (6) ◽  
pp. 877 ◽  
Author(s):  
N Prakash ◽  
AL Lim ◽  
FB Sampson
Keyword(s):  
Mother Cell ◽  
Female Gametophyte ◽  
Cell Plate ◽  
Basic Type ◽  
Ovule Development ◽  
Linear Tetrad ◽  
Polygonum Type ◽  
Secretory Type ◽  
Mother Cells ◽  
Female Gametophyte Development

Three species of Tasmannia R.Br. ex DC., T. glaucifolia, T. insipida and T. stipitata are studied. The anther is tetrasporangiate and its waU development conforms to the Basic type. The tapetum follows the secretory type of development. Cytokinesis in the microspore mother cells is simultaneous but an evanescent cell plate is present at telophase I and anaphase I1 during meiosis. Pollen tetrads are permanent and tetrahedral. The mature pollen is anaulcerate, reticulate and 2-celled. The ovule. is anatropous, bitegmic and crassinucellate. The micropyle in T. stipitata and T. Glaucifolia is formed by the inner integument only whereas in T. insipida it is formed by both the integuments and is zigzag in outline. Meiosis in the single megaspore mother cell produces a linear or T-shaped megaspore tetrad in T. stipitata and T. glaucifolia but only a linear tetrad in T. insipida. Female gametophyte development is of the monosporic Polygonum type. Fertilisation is porogamous; triple fusion and syngamy occur simultaneously.

The floral morphology and embryology of Themeda australis (R. Br.) Stapf

1964 ◽  
Vol 12 (2) ◽  
pp. 157 ◽  
Author(s):  
PS Woodland
Keyword(s):  
Embryo Sac ◽  
Pollen Grains ◽  
Low Fertility ◽  
Linear Tetrad ◽  
Polygonum Type ◽  
Morphological Variations ◽  
Endosperm Formation ◽  
Secretory Type ◽  
Successive Cytokinesis ◽  
Mother Cells

A comparative study was carried out between diploid and tetraploid races of Themeda australis from Armidale and Cobar, respectively. Some morphological variations occur in both populations, but sporogenesis and gametogenesis are identical. The anther is tetrasporangiate and the development of its four-layered wall is described. The tapetum is of the secretory type and its cells become binucleate at the initiation of meiosis in the adjacent microspore mother cells which undergo successive cytokinesis. Microspore tetrads are usually isobilateral and the pollen grains are three-celled at dehiscence, which takes place by lateral longitudinal slits. The ovule is of a modified anatropous form and bitegmic, the broad micropyle being formed of both integuments. The single hypodermal archesporial cell develops directly into the megaspore mother cell and the nucellar epidermis undergoes periclinal and anticlinal divisions to form a conspicuous epistase. The chalaza1 megaspore of the linear tetrad gives rise to a Polygonum-type embryo sac. Material from the Armidale population showed one embryo sac per ovule, but two to five embryo sacs were present in that from Cobar. Embryogeny is typically graminaceous and endosperm formation is at first free-nuclear, later becoming cellular. Polyembryony follows fertilization of several embryo sacs within the same ovule. The reasons for low fertility of T. australis and poor germination of seeds are discussed.

Ovule and female gametophyte development in the Bromeliaceae: an embryological study of Pitcairnia encholirioides

Botany ◽  
2014 ◽  
Vol 92 (12) ◽  
pp. 883-894 ◽  
Author(s):  
Simone P. Mendes ◽  
Alexandra A. Mastroberti ◽  
Jorge E.A. Mariath ◽  
Ricardo C. Vieira ◽  
Karen L.G. De Toni
Keyword(s):  
Life Cycle ◽  
Female Gametophyte ◽  
Ovule Development ◽  
Filiform Apparatus ◽  
Cell Wall Component ◽  
Polygonum Type ◽  
Gametophyte Development ◽  
Structural Alterations ◽  
Female Gametophyte Development ◽  
Advance Knowledge

Pitcairnia encholirioides L.B.Sm. is an endangered species endemic to the Brazilian Atlantic Forest. This species exhibits limited flowering, late seed germination, and preference for clonal growth. Because little is known about its life cycle and female gametophyte development, the ovule development, gynosporogenesis, and gynogametogenesis were analysed to advance knowledge of the species’ life cycle and structural alterations during ovule and female gametophyte development. Also, identification of embryological characters contributing to systematics of Pitcairnioideae is relevant. The ovules are anatropous, bitegmic, and crassinucellate, the gynosporogenesis is monosporic, and the female gametophyte is a Polygonum type. Different patterns in development of the integuments, nucellus, chalazal appendage, and micropylar channel indicate the potential of these characters for subfamily systematics. In the filiform apparatus, a range of glycan-directed monoclonal antibodies was used; the filiform exhibited a biphasic structure. While only arabinogalactan proteins (AGPs) occurred in the translucent matrix, mannans were the most prevalent glycan in the denser matrix. These phases may have distinct mechanical or signalling properties, as they showed different cell wall component distributions. The distinct spatial distribution between AGPs and other glycans showed that the filiform apparatus is heterogeneous and has a common polymer assemblage for both synergids.

scholarly journals The mac1 Gene: Controlling the Commitment to the Meiotic Pathway in Maize

Genetics ◽  
1996 ◽  
Vol 142 (3) ◽  
pp. 1009-1020 ◽  
Author(s):  
William F Sheridan ◽  
Nadezhda A Avalkina ◽  
Ivan I Shamrov ◽  
Tatyana B Batyea ◽  
Inna N Golubovskaya
Keyword(s):  
Female Gametophyte ◽  
Embryo Sac ◽  
Flowering Plants ◽  
Normal Female ◽  
Ovule Development ◽  
Partial Sterility ◽  
Embryo Sac Formation ◽  
Female Gametophyte Development ◽  
Normal Meiosis ◽  
Pleiotropic Mutation

Abstract The switch from the vegetative to the reproductive pathway of development in flowering plants requires the commitment of the subepidermal cells of the ovules and anthers to enter the meiotic pathway. These cells, the hypodermal cells, either directly or indirectly form the archesporial cells that, in turn, differentiate into the megasporocytes and microsporocytes. We have isolated a recessive pleiotropic mutation that we have termed multiple archesporial cells1 (macl) and located it to the short arm of chromosome 10. Its cytological phenotype suggests that this locus plays an important role in the switch of the hypodermal cells from the vegetative to the meiotic (sporogenous) pathway in maize ovules. During normal ovule development in maize, only a single hypodermal cell develops into an archesporial cell and this differentiates into the single megasporocyte. In macl mutant ovules several hypodermal cells develop into archesporial cells, and the resulting megasporocytes undergo a normal meiosis. More than one megaspore survives in the tetrad and more than one embryo sac is formed in each ovule. Ears on mutant plants show partial sterility resulting from abnormalities in megaspore differentiation and embryo sac formation. The sporophytic expression of this gene is therefore also important for normal female gametophyte development.

Embryology of Isotoma petraea

1970 ◽  
Vol 18 (2) ◽  
pp. 213 ◽  
Author(s):  
IC Beltran
Keyword(s):  
Mother Cell ◽  
Embryo Sac ◽  
Endosperm Development ◽  
Ovule Development ◽  
Polygonum Type ◽  
Development Patterns ◽  
Embryo Formation ◽  
Ring Bivalents ◽  
Form Ring ◽  
Embryo Sac Formation

Ovule development, embryo sac formation, and embryogeny of I. Petraea are described. The ovules are anatropous, unitegmic, and tenuinucellar. Meiosis in the megaspore mother cell is regular and the chromosomes with terminalized chiasmata form ring bivalents at metaphase 1. The Polygonum type embryo sac, Scutellaria type endosperm development, and Solanad embryo formation correspond with development patterns in other members of the Lobeliaceae.

scholarly journals Epigenetic Regulation of Plant Gametophyte Development

2019 ◽  
Vol 20 (12) ◽  
pp. 3051 ◽  
Author(s):  
Vasily V. Ashapkin ◽  
Lyudmila I. Kutueva ◽  
Nadezhda I. Aleksandrushkina ◽  
Boris F. Vanyushin
Keyword(s):  
Mother Cell ◽  
Female Gametophyte ◽  
Male Gametophyte ◽  
Endosperm Development ◽  
Epigenetic Changes ◽  
Gametophyte Development ◽  
Daughter Cells ◽  
Second Stage ◽  
Somatic Tissues ◽  
Mother Cells

Unlike in animals, the reproductive lineage cells in plants differentiate from within somatic tissues late in development to produce a specific haploid generation of the life cycle—male and female gametophytes. In flowering plants, the male gametophyte develops within the anthers and the female gametophyte—within the ovule. Both gametophytes consist of only a few cells. There are two major stages of gametophyte development—meiotic and post-meiotic. In the first stage, sporocyte mother cells differentiate within the anther (pollen mother cell) and the ovule (megaspore mother cell). These sporocyte mother cells undergo two meiotic divisions to produce four haploid daughter cells—male spores (microspores) and female spores (megaspores). In the second stage, the haploid spore cells undergo few asymmetric haploid mitotic divisions to produce the 3-cell male or 7-cell female gametophyte. Both stages of gametophyte development involve extensive epigenetic reprogramming, including siRNA dependent changes in DNA methylation and chromatin restructuring. This intricate mosaic of epigenetic changes determines, to a great extent, embryo and endosperm development in the future sporophyte generation.

Megagametogenesis, fertilization, and embryo development in Larixdecidua

1986 ◽  
Vol 16 (6) ◽  
pp. 1301-1309 ◽  
Author(s):  
Grzegorz Kosiński
Keyword(s):  
Cell Wall ◽  
Sexual Reproduction ◽  
Mother Cell ◽  
Megaspore Mother Cell ◽  
Female Gametophyte ◽  
Nuclear Stage ◽  
Empty Seed ◽  
Development Failure ◽  
Major Factors ◽  
Female Gametophyte Development

The phenology of sexual reproduction in Larixdecidua Mill, varies from year to year, and some intra- and inter-clonal differences were also found. Megaspore mother cell meiosis occurred at the time of pollination, during the second half of April, resulting in three or four megaspores. The free nuclear stage and cell wall and archegonia formation were completed in late May and the first half of June. An average of four archegonia was observed in each ovule, but the number ranged from two to six. Fertilization occurred during the first 20 days of June, about 7 weeks after pollination. A four-tiered, 16-celled proembryo formed. Meristematic regions formed in the embryo from the end of June to mid-July. Fully developed embryos were observed in mid-August. Simple polyembryony and delayed cleavage polyembryony were observed. Lack of pollination, disturbances during megasporogenesis and female gametophyte development, failure of fertilization, and embryo degeneration are the major factors resulting in empty seed.

Sexual reproduction of Larix occidentalis

1979 ◽  
Vol 57 (23) ◽  
pp. 2673-2690 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Female Gametophyte ◽  
Pollen Grains ◽  
Larix Occidentalis ◽  
Embryo Abortion ◽  
Meristematic Tissue ◽  
Micropylar Canal ◽  
Empty Seed ◽  
Mother Cells ◽  
Pollen Cone ◽  
Female Gametophyte Development

Pollen-cone and seed-cone buds broke dormancy about 2 weeks before vegetative buds on the same tree. Pollen mother cells, which had over-wintered at pachytene or the diffuse stage of meiosis, resumed meiosis and tetrads of microspores were formed by mid-March. Wingless five-celled mature pollen developed by mid-to late April when pollination occurred.When development resumed after dormancy a ring of meristematic tissue formed the integument around the nucellus. The integument tip developed a short abaxial tip and a large adaxial lobe on which developed numerous long stigmatic hairs. A slit-like micropyle remained between the two lips. Several pollen grains usually adhered to the stigmatic hairs and then the two lips grew into the micropyle, engulfing the pollen. No pollination drop was observed. Within the micropylar canal, pollen greatly elongated then formed a pollen tube when the elongated pollen contacted the nucellus.Megaspore mother cells underwent meiosis at the time of pollination. Female gametophyte development, which was the same as in most other members of the Pinaceae, was completed in early June and two to five archegonia were formed. Fertilization occurred in early June, 6 to 8 weeks after pollination. A 16-celled proembryo developed. Simple polyembryony was common but cleavage polyembryony was not observed. Embryo development was similar to other members of the Pinaceae. Embryos and seeds were mature by mid-August.Normal appearing but inviable seed is common in L. occidentalis because the ovule is fully enlarged and the seed coat well developed at fertilization. Inviable seed commonly resulted from the absence of pollination, inviable pollen, lack of fertilization, later ovule abortion, or embryo abortion, primarily during early embryonic stages. Flat empty seed also occurred and resulted from abortion of the megaspore mother cell or early female gametophyte.

Pollination, female gametophyte, and embryo and seed development in yellow cedar (Chamaecyparis nootkatensis)

1975 ◽  
Vol 53 (2) ◽  
pp. 186-199 ◽  
Author(s):  
John N. Owens ◽  
Marje Molder
Keyword(s):  
Seed Development ◽  
Female Gametophyte ◽  
Pollen Tubes ◽  
Variable Number ◽  
Male Gametes ◽  
Seed Cone ◽  
Complex Forms ◽  
The One ◽  
Mother Cells ◽  
Female Gametophyte Development

After dormancy, both pollen- and seed-cone buds resume development early in April at higher elevations on Vancouver Island. Pollen, formed the previous fall, is shed at the one-celled stage during the last half of April. Pollination occurs during a 2-week period. Pollen frequently germinates and elongates in the pollination drop within the micropyle before reaching the nucellus. Pollen tubes penetrate most of the nucellus during May and early June, then pollen-tube growth slows or stops until mid-July when the pollen tubes quickly extend to the surface of the neck cells and two large, equal-sized male gametes form. Meiosis of the megaspore mother cells occurs during April and early May. Female gametophyte development, similar to that in other members of the Cupressaceae, occurs from late May until late July. An archegonial complex forms with an average of nine archegonia. Fertilization occurs at the end of July and proembryo development begins immediately. A file of four free nuclei forms. Considerable variation exists in subsequent nuclear divisions and cell-wall formation. This may result from the long, narrow archegonia and highly variable number of archegonia. A four-tiered proembryo forms and cleavage polyembryony occurs. The embryos reach the multicellular or the massive stage with secondary suspensors by October when the cones, containing ovules which were pollinated in April, become dormant. Embryo and seed development resume the next April, 1 year after pollination, and development is usually complete in July or August. Embryo development occurs more rapidly near sea level but is complete by fall of the year after pollination at all elevations studied. Most seed is shed early in the fall, but some seed may not be shed until January. The distinction is made between immature 1-year-old and mature 2-year-old seeds and cones. Cones contained an average of 7.2 seeds, of which only 29% were filled.

Studies on the Monimiaceae. III. Gametophyte development of Laurelia novae-zelandiae A. Cunn. (subfamily Atherospermoideae)

1969 ◽  
Vol 17 (3) ◽  
pp. 425 ◽  
Author(s):  
FB Sampson
Keyword(s):  
Generative Cell ◽  
Embryo Sac ◽  
Radial Wall ◽  
Tetrad Stage ◽  
Polygonum Type ◽  
Gametophyte Development ◽  
Pollen Mother Cells ◽  
Secretory Type ◽  
Mother Cells ◽  
Unusual Type

Floral ontogeny and gametophyte development of the New Zealand endemic species Laurelia novae-zelandiae is described. The microsporangium has three to five wall layers inside the epidermis, including a typically thickened endothecium and a tapetum of the secretory type in which the cells become binucleate during the first meiotic division of pollen mother cells. Cytokinesis of pollen mother cells is of an unusual type in which centrifugal cell plates do not develop until the end of meiosis 11. The generative cell of the pollen grain is cut off against what represents a radial wall of the grain with reference to the tetrad stage. Pollen is two- or three-celled when shed. Ovules are bitegmic, crassinucellate, and anatropous with a Polygonum type of embryo sac development.

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