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.

Floral morphology, embryology, and relationships of the Berberidaceae.

1969 ◽  
Vol 17 (1) ◽  
pp. 69 ◽  
Author(s):  
RLN Sastri
Keyword(s):  
Floral Morphology ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Wall Layer ◽  
Vascular Supply ◽  
Anther Wall ◽  
Polygonum Type ◽  
Innermost Layer ◽  
Secretory Type ◽  
Mother Cells

The floral morphology and development of the gametophytes in Berberis umbellata and Mahonia leschenaultii have been studied. All the perianth members have three traces each in B. umbellata while in M. leschenaultii the members of the outer three whorls have five veins each and those of the fourth three veins each. The vascular supply for the inner two whorls of perianth and the stamens arises as conjoint traces. The wall of the gynoecium is traversed by numerous bundles with some concentrated in the placental region. The dorsal and ventral bundles are differentiated in M. leschenaultii but not in B. umbellata. The tricarpellary interpretation of the gynoecium is shown to be unconvincing. The gynoecium is regarded as monocarpellary. The mature anther wall is five-layered including the epidermis, of which the innermost layer forms the tapetum of secretory type. The tapetal cells are four to eight-nucleate. The hypodermal wall layer develops into a fibrous endothecium in M. leschenaultii. In B. urnbellata, the endothecium develops U-shaped thickenings. Division of pollen mother cells is successive. Pollen tetrads are usually isobilateral. Mature pollen grains are three-colpate and two-celled. The ovule is anatropous, bitegmic, and crassinucellate. In B. umbellata, a rudimentary aril is formed as an outgrowth of the funiculus. The single hypodermal archesporial cell in the young ovule cuts off a parietal cell. Development of the embryo sac is of the Polygonum type. The synergids show filiform apparatus and are persistent. The antipodals are large and persistent in M. leschenaultii and ephemeral in B. umbellata. The relationships of the Berberidaceae (sensu Hutchinson 1959) to the Menispermaceae, Lardizabalaceae, and the Ranunculaceae (sensu lato) are discussed.

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.

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.

Embryology and Reproductive Ecology of the Darling Lily, Crinum flaccidum Herbert

1990 ◽  
Vol 38 (5) ◽  
pp. 433 ◽  
Author(s):  
G Howell ◽  
N Prakash
Keyword(s):  
Pollen Grains ◽  
Mature Embryo ◽  
Microspore Mother Cell ◽  
Polygonum Type ◽  
Binucleate Cells ◽  
Cell Layers ◽  
Nectar Sugar ◽  
Endosperm Formation ◽  
Successive Cytokinesis ◽  
Seed Coats

In Crinum flaccidum the anthers are versatile and tetrasporangiate with a secretory tapetum of binucleate cells. Successive cytokinesis in microspore mother cell results in isobilateral and decussate microspore tetrads. The mature pollen grains are single, spheroidal, disulculate, echinate and 2-celled. In the mature anthers, fibrous thickenings develop not only in the endothecium but also in two or three middle cell layers and the connective tissue before latrorse dehiscence. A lobed tissue in each of the three locules of the ovary serves ovular and placental functions. Each extension of the 5-7 paired lobes represents an ategmic ovule. The development of the female gametophyte conforms to the Polygonum type. Usually only one gametophyte is present in each lobe but occasionally several may occur. Bulb growth is monopodial with normally three umbels produced per plant, each carrying an average of 10 flowers, only two or three of which are open at any one time. Nectar sugar concentration was measured at 14.2% (w/w), of which 44.8% of solids was sucrose and 3.9% either glucose or fructose. The protandrous flowers are phalenophilous, pollinated by sphingid moths. The endosperm formation is of the nuclear type. In the absence of seed coats and the nucellus at maturity, the outer layers of the endosperm become corky following the activity of a phellogen. Embryogeny appears to be of the Asterad type. The mature embryo is straight and chlorophyllous. The large (5.3 g) seeds are 89% water and show no dormancy, germinating without an external supply of water, sometimes while still on the parent plant.

Studies on the Monimiaceae. I. Floral morphology and gametophyte development of Hedycarya arborea J.R. et.G. Forst. (subfamily Monimioideae)

1969 ◽  
Vol 17 (3) ◽  
pp. 403 ◽  
Author(s):  
FB Sampson
Keyword(s):  
Cell Division ◽  
Floral Morphology ◽  
Generative Cell ◽  
Embryo Sac ◽  
Polygonum Type ◽  
Australian Species ◽  
Tapetal Cells ◽  
Pollen Traps ◽  
Secretory Type ◽  
Mother Cells

Inflorescences, flowers, and floral vascularization of the New Zealand endemic species Hedycarya arborea are described. Varying carpel vasculature suggests derivation of the uniovulate condition in Hedycarya from ancestors having multiovulate carpels with ovules in two rows, Floral ontogeny is described and it is noted that the terminal stigmatic region of the carpel develops from a solid terminal meristem, in contrast to many woody Ranales in which the stigma consists of crests surrounding the carpel cleft. The stigmatic surface is a mass of globose projections, apparently serving as pollen traps. No comparable type of stigma has previously been reported in the woody Ranales. The microsporangium has a typically thickened endothecium and a tapetum of the secretory type with tapetal cells becoming binucleate during the first meiotic division of pollen mother cells. Pollen mother cell division is of the successive type with cytokinesis by centrifugally extending cell plates. The generative cell is cut off towards the distal face of the microspore. The pollen, in permanent tetrads, is shed in the two-celled condition. Ovules are bitegmic, crassinucellate, and anatropous with a Polygonum type of embryo sac development. Some comparisons are made with the Australian species Hedycarya angustifolia.

The embryology of Kunzea capitata Reichb

1969 ◽  
Vol 17 (1) ◽  
pp. 97 ◽  
Author(s):  
N Prakash
Keyword(s):  
Outer Integument ◽  
Cell Formation ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Basic Type ◽  
Ring Stage ◽  
Polygonum Type ◽  
Signet Ring ◽  
Mother Cells ◽  
Antipodal Cells

The anther is tetrasporangiate and the development of its wall is of the Basic type. Ubisch granules are formed on the surface of the tapetum at the signet-ring stage of the pollen grains. The anther dehisces by longitudinal slits, and pollen grains are shed at the two-celled stage. The female archesporium is subepidermal and cuts off the primary parietal cell. A six-layered parietal tissue is formed below the nucellar epidermis by the time megasporogenesis is completed. The flowers are protandrous, and in any given bud meiosis in megaspore mother cells follows that in microspore mother cells. Embryo sac development is of the Polygonum type and the antipodal cells are ephemeral. Cell formation in the nuclear endosperm commences at the micropylar end and proceeds towards the chalaza. Embryogeny corresponds to the Onagrad type and no evidence of polyembryony was found. Both the integuments take part in the formation of the seed coat, in which the cells of the outer layer of the outer integument are conspicuously elongated. A comparison is made with the embryological findings in other myrtaceous plants.

A contribution to the life history of Angophora floribunda (Sm.) Sweet (Myrtaceae)

1969 ◽  
Vol 17 (3) ◽  
pp. 457 ◽  
Author(s):  
N Prakash
Keyword(s):  
Floral Development ◽  
Outer Integument ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Flower Buds ◽  
Polygonum Type ◽  
Mature Embryos ◽  
History Of ◽  
Sterile Pollen ◽  
Mother Cells

The flower buds of Angophora floribunda appear in the last week of November and anthesis occurs in the middle of January the following year. There is no prolonged resting phase at any stage during embryology and the seeds are shed during late February to early March. In floral development, the petals are the last structures to be formed. Early anther development precedes corresponding stages in the ovules of the same flower, but events in the ovules proceed more rapidly and meiosis occurs simultaneously in the spore mother cells of both organs. The mature two-celled pollen grains are shed when the ovules contain four-or eight-nucleate embryo sacs. Many flowers bear anthers containing only sterile pollen grains, which occur either singly or as tetrads. Various abnormalities in the development of the pollen are reported, and the anthers containing sterile pollen neither develop fibrous bands in the endothecium nor do they dehisce. The ovules are bitegminal, crassinucellar, and hemianatropous. Occasional bifurcation of the inner integument was observed and a hypostase differentiates at the four-nucleate stage of the embryo sac. The embryo sac follows the Polygonum type of development and is five-nucleate and four-celled when mature. The endosperm is Nuclear in origin, and in about half the seeds examined a granular unidentified substance accumulates in the embryo sac. The development of the embryo is irregular and the seedlings bear a collar-like structure at the junction of the hypocotyl and the radicle. The mature embryos are usually dicotyledonous but rarely tricotyledonous. The seed coat is formed exclusively by the outer integument; in the ripe seed it consists of an outer epidermis of large, palisade-like, thin-walled, tanniniferous cells and an inner crystalliferous layer.

Embryological studies in the compositae. IV. Sporogenesis, gametogenesis, and embryogeny in Brachycome ciliaris (Labill.) Less

1964 ◽  
Vol 12 (2) ◽  
pp. 142 ◽  
Author(s):  
GL Davis
Keyword(s):  
New South ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Egg Cell ◽  
Male Sterile ◽  
Morphological Variations ◽  
Secondary Nucleus ◽  
South Wales ◽  
Mother Cells ◽  
Antipodal Cells

Material of two varieties of Brachycome ciliaris was obtained from several localities in southern Queensland and western New South Wales, and no embryological differences were found between populations in spite of considerable morphological variations. The plant was highly male-sterile, and although development of the anthers was normal up to the formation of microspore mother cells, presumed meiotic abnormalities resulted in failure to form microspore tetrads except in one instance. The formation of plasmodial microspore mother cells and unreduced pollen grains is described and the occurrence of normal pollen grains in two capitula is recorded. In the ovule, meiosis is suppressed and the megaspore mother cell becomes vacuolate and functions directly as the uninucleate embryo sac. Three nuclear divisions precede the formation of an eight-nucleate embryo sac in which the antipodal cells undergo secondary multiplication. There is circumstantial evidence that the polar nuclei divide simultaneously to form the fist four endosperm nuclei and do not first fuse to form a secondary nucleus. The egg cell develops parthenogenetically and cleavages follow the asterad type of development. The eariy stages of embryogeny are completed before the opening of the florets.

Life history of Tetragonia tetragonioides (Pall.) O. Kuntze

1967 ◽  
Vol 15 (3) ◽  
pp. 413 ◽  
Author(s):  
N Prakash
Keyword(s):  
Cell Formation ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Mature Embryo ◽  
Polygonum Type ◽  
Innermost Layer ◽  
Glandular Cells ◽  
History Of ◽  
Mother Cells ◽  
Tetragonia Tetragonioides

Accessory flowers arise from the surface of inferior ovaries in 25 % of the flowers of Tetragonia, suggesting an axial nature of the inferior ovary. The ovary is six to nine-loculed, with a single pendulous ovule in each locule. The anther is tetrasporangiate. The innermost layer of the four-layered wall constitutes a secretory tapetum with multinucleate cells. Cytokinesis in microspore mother cells is simultaneous and results in tetrahedral or decussate tetrads. The pollen grains are shed at the three-celled stage. The ovules are bitegminal, crassinucellar, and anacampylotropus. The funiculus is long and bears an obturator of glandular cells. The inner integument forms the micropyle and forms a collar at the distal end. A nucellar cap is present. The nucellus persists in the seed as perisperm. The archesporium is multicelled, although only a single cell develops. Following meiosis the megaspore mother cell gives rise to a linear row of three or four megaspores, of which only the chalaza1 functions to form an embryo sac of the Polygonum type. The endosperm is of the Nuclear type and eventually assumes a horseshoe shape. Cell formation is restricted to the micropylar region, the rest remaining nuclear until consumed by the embryo. The embryogeny is of the Solanad type, and the mature embryo is curved and dicotyledonous.

Morphological and embryological studies in Nymphaeaceae. II. Brasenia schreberei Gmel. and Nelumbo nucifera Gaertn

1965 ◽  
Vol 13 (3) ◽  
pp. 379 ◽  
Author(s):  
P Khanna
Keyword(s):  
Embryo Sac ◽  
Pollen Grains ◽  
Pollen Sterility ◽  
Nelumbo Nucifera ◽  
Primary Endosperm Nucleus ◽  
Polygonum Type ◽  
Globular Stage ◽  
Compound Pollen ◽  
Mother Cells ◽  
Antipodal Cells

The stamens are whorled in Brasenia schreberei and spirally arranged in Nelumbo nucifera. The anther is tetrasporangiate. Parietal layers are five-celled in thickness in B. schreberei and six-celled in N. nucifera. Endothecial cells contain a tannin-like substance and develop fibrous thickenings in N. nucifera. The middle layers are persistent in N. nucifera and ephemeral in B. schreberei. The tapetal cells become multinucleate and the layer develops cutinization on its inner walls in N. nucifera. It is secretory. Micronuclei are formed at the meiosis in the microspore mother cells. These degenerate in B. schreberei and form micropollen grains in N. nucifera. Polysporads and compound pollen grains occur frequently in the latter. Pollen sterility is common. In B. schreberei the carpel is horseshoe-shaped, unites with its margins, and bears two to three pendulous ovules with lamina1 placentation. The carpel in N. nucifera, however, remains open in its early development, unites by the growth of the interlocking hairs, and contains a single ovule. A single parietal layer is present in B. schreberei, and four to five such layers in N. nucifera. A hypostase is formed in B. schreberei. The nucellus functions as perisperm in the latter and is consumed early in N. nucifera. A linear megaspore tetrad is formed in which the chalazal megaspore is functional. The embryo sac is of the Polygonum type. The antipodal cells are ephemeral in B. Schreberei and persistent with secondary multiplication in N. nucifera. In post-fertilized ovules one of the synergids is persistent. Fertilization is non-synchronous in N. nucifera and simultaneous in B. schreberei. In N. nucifera the antipodal cells become enlarged and multinucleate, and occupy the elongated tube formed by the downward penetration of the embryo sac. They degenerate at the early globular stage of the embryo and are not persistent when the embryo is pear-shaped. In B. schreberei a transverse cytokinesis follows division of the primary endosperm nucleus and two unequal cells are formed. The small chalazal endosperm cell penetrates the nucellus below and forms a long tube-like haustorium occupying three-quarters of the length of the nucellus. Its nucleus subsequently hypertrophies and degenerates completely at the globular stage of the embryo. Endosperm is ab initio cellular in B. schreberei and free nuclear in N. nucifera.

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