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

1969 ◽  
Vol 17 (3) ◽  
pp. 457 ◽  
Author(s):  
N Prakash

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.

1969 ◽  
Vol 17 (1) ◽  
pp. 97 ◽  
Author(s):  
N Prakash

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.


1967 ◽  
Vol 15 (3) ◽  
pp. 413 ◽  
Author(s):  
N Prakash

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.


1969 ◽  
Vol 17 (2) ◽  
pp. 215 ◽  
Author(s):  
N Prakash

In Darwinia the floral parts are differentiated in a "calyx-orolla-gynoeciumandroecium" sequence. In individual buds stages of microsporogenesis markedly precede corresponding stages of megasporogenesis. The anther is tetrasporangiate with all sporangia lying in one plane. The secretory tapetum is one- to three-layered within the same microsporangium and a large number of Ubisch bodies are formed. The anthers dehisce by minute lateral pores and an ingenious mechanism helps disperse the twocelled pollen grains. A basal placenta in the single loculus of the ovary bears four ovules in D. micropetala and two in D. fascicularis. In both species, however, only one ovule is functional after fertilization. The fully grown ovules are anatropous, crassinucellar, and bitegmic; the inner integument forms the micropyle. The parietal tissue is most massive at the completion of megasporogenesis but is progressively destroyed later. The embryo sac follows the Polygonum type of developnlent and when mature is five-nucleate, the three antipodals being ephemeral. Following fertilization, the primary endosperm nucleus divides before the zygote. Subsequent nuclear divisions in the endosperm mother cell are synchronous and lead to a free-nuclear endosperm which becomes secondarily cellular, starting from the micropylar end at the time the globular embryo assumes an elongated shape. Embryogeny is irregular and the mature embryo is straight with a massive radicle and a hypocotyl which terminates in two barely recognizable cotyledons. Sometimes the minute cotyledons are borne on a narrow neck-like extension of the hypocotyl. A suspensor is absent. Both integuments are represented in the seed coat and only the outer layer of the outer and the inner layer of the inner integuments, with their thick-walled tanniniferous cells, remain in the fully grown seed. The ovary wall is demarcated into an outer zone containing oil glands surrounded by cells containing a tannin-like substance and an inner zone of spongy parenchyma. In the fruit this spongy zone breaks down completely but the outer zone is retained. The two species of Darwinia, while closely resembling each other in their embryology, differ significantly from other Myrtaceae. However, no taxonomic conclusions are drawn at this stage, pending enquiry into the life history of other members of the tribe Chamaelaucieae.


1964 ◽  
Vol 12 (2) ◽  
pp. 157 ◽  
Author(s):  
PS Woodland

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.


1969 ◽  
Vol 17 (1) ◽  
pp. 69 ◽  
Author(s):  
RLN Sastri

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.


1965 ◽  
Vol 13 (3) ◽  
pp. 379 ◽  
Author(s):  
P Khanna

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.


Biologia ◽  
2011 ◽  
Vol 66 (2) ◽  
Author(s):  
Abdilkarim Chehregani ◽  
Fariba Mohsenzadeh ◽  
Nayereh Tanaomi

AbstractMale and female gametophytes have special characters that show a great variety in different taxa. In this study, gametophytes of four species belonging to three sections of the genus Onobrychis Mill. were studied with light microscopy. Results showed that the ovular primordium is tetra-zonate and gives rise to an anatropous ovule. The archesporium may consist of one or more archeosporial cells, but only one of them undergoes meiosis, forming a linear or T-shaped tetrad. Normally, only a single megaspore is functional which is located in the chalazal position while the others degenerate very soon. The young ovule is hemi-anatropous but the mature is anatropous, crassinucellar and bitegmic; integuments form a zig-zag micropyle. A 7-celled embryo-sac is formed corresponding to the Polygonum type. Based on our results, the ovular variable characters are the form and condition of ovary, presence or absence of ovary peduncle, the number and condition of ovule in ovary, length and width of ovule, length and width of embryo sac, number of layers in outer integument, condition of megaspore, alignment pattern of the integuments, asymmetrical initiation of the outer integument, shape of tetrad with the presence of one functional megaspore and so on. The separator characters in male gametophyte are including tri-cellular pollen grains and the number of tapetum nuclei. According to our study the female gametophyte characters are more variable than male gametophyte. The present study provides the first report on embryological description in the genus Onobrychis and also in section Heliobrychis.


The Nucleus ◽  
2021 ◽  
Author(s):  
Fajarudin Ahmad ◽  
Yuyu S. Poerba ◽  
Gert H. J. Kema ◽  
Hans de Jong

AbstractBreeding of banana is hampered by its genetic complexity, structural chromosome rearrangements and different ploidy levels. Various scientific disciplines, including cytogenetics, linkage mapping, and bioinformatics, are helpful tools in characterising cultivars and wild relatives used in crossing programs. Chromosome analysis still plays a pivotal role in studying hybrid sterility and structural and numerical variants. In this study, we describe the optimisation of the chromosome spreading protocol of pollen mother cells focusing on the effects of standard fixation methods, duration of the pectolytic enzyme treatment and advantages of fluorescence microscopy of DAPI stained cell spreads. We demonstrate the benefits of this protocol on meiotic features of five wild diploid Musa acuminata bananas and a diploid (AA) cultivar banana “Rejang”, with particular attention on pairing configurations and chromosome transmission that may be indicative for translocations and inversions. Pollen slides demonstrate regular-shaped spores except “Rejang”, which shows fertile pollen grains of different size and sterile pollen grains, suggesting partial sterility and unreduced gamete formation that likely resulted from restitutional meiotic divisions.


1962 ◽  
Vol 10 (1) ◽  
pp. 1 ◽  
Author(s):  
GL Davis

Cotula australis has a discoid heterogamous capitulum in which the outermost three whorls of florets are female and naked. The bisexual disk florets are fully fertile and have a four-lobed corolla with four shortly epipetalous stamens. The anthers contain only two microsporangia. Wall formation and microsporogenesis are described and the pollen grains are shed at the three-celled condition. The ovule is teguinucellate and the hypodermal archesporial cell develops directly as the megaspore mother cell. Megasporogenesis is normal and the monosporio embryo sac develops from the chalazal megaspore. Breakdown of the nucellar epidermis takes place when the embryo sac is binucleate and its subsequent development follows the Polygonum type. The synergids extend deeply into the micropyle and one persists until late in embryogeny as a haustorium. The development of the embryo is of the Asterad type, and the endosperm is cellular. C. coronopifolia agrees with C. australis in the presence of only two microsporangia in each anther and the development of a synergid haustorium.


10.12737/2227 ◽  
2014 ◽  
Vol 8 (4) ◽  
pp. 130-133
Author(s):  
Наимов ◽  
Alisher Naimov ◽  
Меликов ◽  
Kurbonali Melikov ◽  
Партоев ◽  
...  

The article presents the results of a study on the features on the formation of generative organs of potato (Solanum tuberosum L.) in mountainous areas of Tajikistan at a height of over 2700 meters above sea level. There is a difference in formation character of generative system of potato plants, depending on the genotype accessions. It was noted that the formation of flower buds on the total amount of from 5 to 95%, and the number of berries formed 1to 10 units /plant or from 7.7 to 20.6 % of the total number of flowers. Formation of berries of potato varieties in a little due to the amount of viable pollen grains per flower. The number of seeds in a berry varies from 51 to 150 units, and it is associated with the viability of the pollen grains of potato flower. One berry of potatoes in average contains about 96 pieces of seeds. It was determined that 16 % of potato accessions form less than 10 % have viable pollen grains, which is probably due to a partial cytoplasmic sterile pollen.


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