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.

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.

Apomixis and abnormal anther development in Calotis lappulacea Benth. (Compositae)

1968 ◽  
Vol 16 (1) ◽  
pp. 1 ◽  
Author(s):  
GL Davis
Keyword(s):  
New South ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Anther Wall ◽  
Male Gametes ◽  
Globular Stage ◽  
South Wales ◽  
Vertical Division ◽  
Endosperm Formation ◽  
Embryo Sac Formation

A comparative study was made of material collected from four localities in New South Wales and Queensland and a number of embryological aberrations were found to be common to all districts. During microsporogenesis, certain tapetal cells not only failed to contribute to the tapetal periplasmodium but, after increasing in size, they separated from the anther wall and resembled one-, two-, or four-nucleate embryo sacs developing among the microspores. In one anther a structure was present which was very similar to a fully differentiated embryo sac. Although the pollen grains of some anthers contained male gametes, most anthers dehisced when the pollen was two-celled and some shrivelled soon after meiosis. Megasporogenesis was followed by the formation of linear tetrads of megaspores, but embryo sac formation was the result of somatic apospory and C. lappulacea appears to be an obligate apomict. The enlarging somatic cell usually invades the nucellar lobe and replaces the megaspores but one or more such celis commonly develop also in the chalaza, and up to eight embryo sacs were found in one ovule. Enlargement of a chalazal embryo sac sometimes resulted in penetration of the ovular epidermis and its invasion of the loculus as a haustorium-like structure. Extrusion of a developing embryo sac through the micropyle was common. Embryogeny is of the Asterad type, but vertical division of the terminal cell ca was delayed until after the basal cell cb had given rise to superposed cells m and ci. Polyembryony was common but only one embryo in each ovule reached maturity. Endosperm formation was independent of embryogeny but unless it was initiated before the globular stage of the embryo, the embryo sac collapsed and the embryo degenerated.

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.

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.

Evidence of a geographical variation in Mesochaetopterus (Polychaeta: Chaetopteridae) from the Pacific Ocean

2005 ◽  
Vol 85 (6) ◽  
pp. 1409-1423 ◽  
Author(s):  
Michel R. Bhaud
Keyword(s):  
Pacific Ocean ◽  
New South ◽  
Solomon Islands ◽  
New South Wales ◽  
Morphological Variations ◽  
Geographical Variations ◽  
South Wales ◽  
The Pacific ◽  
The Pacific Ocean ◽  
Hard Structures

Specimens of Mesochaetopterus (Chaetopteridae) from seven geographical sources in the Pacific Ocean are compared on the basis of their hard structures: specialized chaetae, uncinal plates and tubes. There geographical variations are investigated both locally (New South Wales and the Solomon Islands) and over the whole Pacific Ocean from Australia (New South Wales) through the Solomon Islands to Galapagos and Hawaii. The most interesting result is the existence of intra-regional morphological variations with the hard structures differing on specimens sampled in two areas from New South Wales or in two areas from the Solomon Islands out of a total of three areas. These newly described morphologies imply that M. minutus, isolated in a first step from M. sagittarius and confined to the Pacific, is a pseudo-sibling species complex. Each element of this complex is morphologically distinguishable. Consequently the generally accepted role of the long-lived planktonic larvae characteristic of Mesochaetopterus, as a source of geographical homogeneity must be re-examined.

Chromosomal Differentiation Among Ecotypes of Phalaris aquatica L.

1980 ◽  
Vol 28 (6) ◽  
pp. 645 ◽  
Author(s):  
E Putievsky ◽  
RN Oram ◽  
K Malafant
Keyword(s):  
Pollen Grains ◽  
F1 Hybrids ◽  
Male Sterile ◽  
Geographic Origins ◽  
Meiotic Irregularities ◽  
Structural Differences ◽  
Two Generations ◽  
Chromosomal Differentiation ◽  
Mother Cells ◽  
F2 Progeny

Seventy-two hybrids of P. aquatica were made among 13 diverse Mediterranean ecotypes and cv. Australian, and five indicators of hybrid abnormality were measured in the first two generations. The proportions of stainable, apparently normal pollen grains formed by F, hybrids varied between 5 and 98% and their spikelet fertility ranged from 19 to 77%. Of the 43 hybrids that were derived from pairs of self-incompatible parents, 13 were highly self-compatible. Crosses between lines from different groups of parents produced F2 progeny containing up to 17% of lethal seedlings and up to 39% of male sterile plants. In the cross between cv. Australian and the Moroccan ecotype, CPI 19331: the frequency ofzebra-striped lethal seedlings was as high as 33% in F2 progenies, but only 0 or 1% in back-crosses to either parent. Hence the zebra-striped phenotype was not caused by a mutation existing in the parents but rather by deletions or duplications generated during meiosis in the F1 hybrids. Many meiotic irregularities were observed in the pollen mother cells of the F1 and F2 hybrids between cv. Australian and CPI 19331. These included small loops, acentric fragments, univalents and multivalents at diakinesis, and bridges at anaphase I, indicating that the genomes of these two lines differed by several inversions and interchanges. These structural differences would lead to a range of duplications and deficiencies in the gametes. and hence could account for each of the five kinds of hybrid abnormality observed in the F1 and F2 generations. One aneuploid F2 plant with 25 chromosomes was found. A dihaploid plant in cv. Australian had an average of 4.3 bivalents per pollen mother cell, whereas virtually all chromosomes in the tetraploid parental lines paired as bivalents. Thus, P. aquatica is a segmental allotetraploid with a system which prevents homoeologous pairing in tetraploids but not in dihaploids. The partial barriers to hybridization between P. aquatica lines are not closely related to their geographic origins or varietal classifications. These barriers may hinder but have not prevented the recombination of parental traits during the development of improved cultivars.

Apospory in Paspalum thunbergii

2004 ◽  
Vol 52 (1) ◽  
pp. 81 ◽  
Author(s):  
Guohua Ma ◽  
Xuelin Huang ◽  
Nanxian Zhao ◽  
Qiusheng Xu
Keyword(s):  
Chromosome Number ◽  
Developmental Stage ◽  
Pollen Viability ◽  
Paraffin Section ◽  
Embryo Sac ◽  
Low Frequency ◽  
The Other ◽  
Egg Cell ◽  
Successive Generations ◽  
Mother Cells

The cytology, development of aposporous embryo sac, pro-embryo and pseudogamy in Paspalum thunbergii Kunth ex Steud. was studied. P. thunbergii was found to be a tetraploid cytotype, with a chromosome number of 40. Meiosis of the pollen mother cells was irregular, pollen viability was low and multiporate pollens were often observed. Megasporogenesis began normally; however, the megaspore deteriorated at the developmental stage of tetrad, while one to five specific nucellar cells became active and began enlarging, and then developed into aposporous embryo sacs. The mature aposporous sacs usually had three nuclei characterised by one egg cell and two polar nuclei. The egg cell developed spontaneously to form pro-embryos prior to anthesis. When several aposporous sacs occurred in the same ovule, usually one sac near the micropyle was involved in pseudogamy, while the other sacs were not involved. Low frequency of twin-embryo seedlings was observed after seeds matured. Examination of three successive generations by paraffin-section and clearing methods revealed that no sexual sac was present. Therefore, the species P. thunbergii is considered to be an obligate apomict that reproduces by apospory.

scholarly journals Development of generative structures of polar Caryophyllaceae plants: the Arctic Cerastium alpinum and Silene involucrata, and the Antarctic Colobanthus quitensis

2017 ◽  
Vol 38 (1) ◽  
pp. 83-104 ◽  
Author(s):  
Wioleta Kellmann-Sopyła ◽  
Justyna Koc ◽  
Ryszard J. Górecki ◽  
Marcin Domaciuk ◽  
Irena Giełwanowska
Keyword(s):  
Embryo Sac ◽  
Single Layer ◽  
Pollen Grains ◽  
The Arctic ◽  
Egg Cell ◽  
Colobanthus Quitensis ◽  
West Antarctic ◽  
The Family ◽  
Electron Microscopes ◽  
Species Specific

AbstractThe embryology of three polar flowering plants of the family Caryophyllaceae was studied using the methods and techniques of the light, normal and fluorescence microscopes, and the electron microscopes, scanning and transmission. The analyzed species wereColobanthus quitensisof West Antarctic (King George Island, South Shetlands Islands) as well asCerastium alpinumandSilene involucrataof the Arctic (Spitsbergen, Svalbard). In all evaluated species, flowering responses were adapted to the short Arctic and Australian summer, and adaptations to autogamy and anemogamy were also observed. The microsporangia of the analyzed plants produced small numbers of microspore mother cells that were differentiated into a dozen or dozens of trinucleate pollen grains. The majority of mature pollen grains remained inside microsporangia and germinated in the thecae. The monosporous Polygonum type (the most common type in angiosperms) of embryo sac development was observed in the studied species. The egg apparatus had an egg cell and two synergids with typical polarization. A well-developed filiform apparatus was differentiated in the micropylar end of the synergids. In mature diaspores of the analyzed plants of the family Caryophyllaceae, a large and peripherally located embryo was, in most part, adjacent to perisperm cells filled with reserve substances, whereas the radicle was surrounded by micropylar endosperm composed of a single layer of cells with thick, intensely stained cytoplasm, organelles and reserve substances. The testae of the analyzed plants were characterized by species-specific primary and secondary sculpture, and they contained large amounts of osmophilic material with varied density. Seeds ofC. quitensis,C. alpinumandS. involucrataare very small, light and compact shaped.

scholarly journals Embryological studies on Anthemis tinctoria L.

2015 ◽  
Vol 46 (4) ◽  
pp. 547-557 ◽  
Author(s):  
K. Bijok ◽  
T. Pawlak ◽  
B. Kreńska
Keyword(s):  
Chromosome Number ◽  
Embryo Development ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Natural Habitats ◽  
Antipodal Cells

The chromosome number of <i>Anthemis tinctoria</i> from natural habitats in Poland is n=9. The development of pollen grains is normal. The embryo-sac is of tetrasporic type and the number of antipodal cells is seven, all derived from one-cellular archespore. The embryo development is of Aster type and the endosperm is of nuclear type.

scholarly journals Studies on the Morphology, Ontogeny and Embryology of the Flowers of Hedycarya Arborea J.R. et G. Forst. (Subfamily Monimioideae) and Laurelia Novae-Zelandiae A. Cunn. (Subfamily Atherospermoideae) of the Family Monimiaceae

2021 ◽  
Author(s):  
◽  
Frederick Bruce Sampson
Keyword(s):  
Generative Cell ◽  
Embryo Sac ◽  
Pollen Grains ◽  
Tetrad Stage ◽  
Pollen Mother Cells ◽  
The Family ◽  
Long Time ◽  
External Part ◽  
Mother Cells ◽  
And Function

<p>The inflorescences, flowers and the vascularization of floral parts of Hedycarya arborea and Laurelia novae-zelandiae were described and comparisons made with other members of the family in an attempt to determine the basic types of inflorescences, flowers and floral vascularization in the family. The vegetative, inflorescence and floral meristems of the two genera were compared. It was concluded that the vegetative apices of both had the tunica-corpus configuration typical of many other woody Ranales and other orders. The inflorescence apices were quite similar to the vegetative ones. The young floral apices are in a state of transition from a tunica-corpus to a mantle-core configuration and older floral apices had the mantle-core configuration, which is typical of the floral apices of many woody Ranales. Unusual features of the floral apices of Hedycarya and Laurelia were the lack of a pronounced rib meristem and the occurrence of relatively frequent divisions within vacuolate cells of the core. The ontogeny of the stamens of Hedycarya and Laurelia was described and comparisons were made. In both genera the micro-sporangium developed in a similar fashions: in Hedycarya 5-6 wall layers are formed inside the epidermis; in Laurelia there are 3-5 layers. Both genera had a typically thickened endothecium and a tapetum of the secretory type in which the tapetal cells become binucleate during the first meiotic division of the pollen mother cells. In Hedycarya the meiotic divisions of the pollen mother cells are of the successive type in which walls form by means of centrifugal cell plates Pollen grains remain in permanent tetrads in this genus. In Laurelia wall formation at the end of meiosis is of a modified simultaneous type, which may not have been hitherto described in the literature. Pollen grains are not in permanent tetrads. When the first division occurs in each microspore in Hedycarya, all four cells of a tetrad are at the same stage of division and the generative cell is cut off towards the distal face of the grain. Each microspore is in the two celled condition when shed. It was deduced that the generative cell is cut off against what represents a radial wall of the grain (with reference to the tetrad stage) in Laurelia. Pollen is shed in either the two or three celled condition. Comparisons were made with the development of microsporangia and male gametophytes in other woody Ranales. A study was made of the ontogeny, structure and function of the staminal appendages of Laurelia. It was found that the appendages function as nectaries, the nectar being predominantly sucrose. After a discussion of the various theories as to the morphological nature of the staminal appendages of the Laurales, it was concluded that they are morphologically staminodes. The carpels of Hedycarya and Laurelia have a basically similar ontogeny in which, as in the Lauraceae, the terminal stigmatic region develops from a solid terminal meristem in contrast to many woody Ranales in which the stigma-consists of crests which surround the external part of the cleft of the carpel. The ovules of Hedycarya and Laurelia resemble those of most other woody Ranales in being bitegmic, crassinucellate and anatropous with a monosporic 8-nucleate embryo sac of the Polygonum type. Both linear and T-shaped megaspore tetrads were found in the two genera. Laurelia has pseudocarps which develop after anthesis and enclose plumose achenes, but in Hedycarya the fruits are drupes. It was concluded that Laurelia and Hedycarya belong to two subfamilies which have been separated from each other for a long time and have undergone considerable evolution in different directions. It was also concluded that the Monimiaceae are closely related to the Lauraceae.</p>

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