Microsporogenesis in the normal and male-sterile stamenIess-2 mutant of tomato (Lycopersicon esculentum)

1988 ◽  
Vol 66 (10) ◽  
pp. 2013-2021 ◽  
Author(s):  
V. K. Sawhney ◽  
S. K. Bhadula

The development of microspores and the associated changes in the tapetum were examined in the normal (+/+) and male-sterile, stamenless-2 (sl-2/sl-2) mutant anthers of tomato (Lycopersicon esculentum). Anthers of eight comparable stages, from the microspore mother cell stage to anthesis, of both lines were processed for light microscopy. Until the formation of tetrads (stage ii), there were no differences in the sporogenous tissue, but the tapetal cells of the mutant were more enlarged than the normal and had, at places, divided to form a bilayer. Later, the tapetal cells in both lines became amoeboid and had sporopollenin-like deposits. At stage iv, whereas the tapetal cells of the normal had started to degenerate, those of the mutant were intact but had large vacuoles. Also at this stage, the deposition of exine was evident in normal microspores, but it was lacking in most mutant microspores, which enlarged considerably and eventually degenerated. From stage v onwards, the normal microspores progressed from the binucleate pollen to pollen containing many vacuoles to mature pollen. In the mutant, tapetum degeneration was delayed until stage v, and later, although some microspores closer to the tapetum appeared normal, most either were empty or had large vacuoles. It is suggested that the delay in tapetum degeneration coupled with the failure of exine deposition, presumably associated with low esterase activity, is responsible for pollen degeneration in the sl-2/sl-2 mutant.

1979 ◽  
Vol 57 (6) ◽  
pp. 578-596 ◽  
Author(s):  
P. C. Cheng ◽  
R. I. Greyson ◽  
D. B. Walden

Anther ontogeny of a genic male-sterile mutant (ms 10/ms 10) and a related fertile cultivar of Zea was studied from the primordial stage through to tassel maturity. From material glutaraldehyde–formalin fixed, OsO4 postfixed, and plastic embedded, light microscopy of 0.7-μm sections revealed no developmental differences between the two until the young microspore stage. Vacuolation or cytoplasmic disintegration of tapetal cells was detected in male-sterile anthers at this stage. Disintegration of microspores was not detected until the intermediate microspore stage. By the young pollen stage, tapetal cells were highly disorganized and degeneration of the middle layer and endothecium was apparent. No endothecial wall thickenings developed in male-sterile anthers.In normal anther development in Zea, endothecial thickenings are found only at the anterior and posterior ends of the anther. A highly ridged anther cuticle, which is essentially absent in male-sterile anthers, is a common feature of fertile flowers. Anther dehiscence involves a separation of the epidermis from the underlying parenchyma of the connective to form a large pollen cavity from the two microsporangial locules. This process does not involve endothecial fibrous wall thickenings as they are not present over the bulk of the anther. Formation of the anterior pore is a separate process which involves changes in the endothecium wall thickenings.During normal anther development starch accumulates in the endothecium and epidermis at the precallose stage and disappears during the young microspore stage. No differences were noted in the male-sterile anthers. During the formation of normal pollen, considerable starch accumulation is evident. However, none is deposited at this late stage in the male-sterile anther.


1970 ◽  
Vol 7 (7) ◽  
pp. 37-40 ◽  
Author(s):  
Mohammed Inamuddin ◽  
Beatrice Were ◽  
Mohammad Saquib

The present investigation deals with morphological and embryological studies of Rhynchelytrum repens (Willd) C.E. Hubbard. The development of anther walls are found to be Monocotyledonous type. The tapetal cells are substantially large, glandular and uninucleate. The middle layer is ephemeral and their cells are small in size. It is sandwiched between endothecial and tapetal layer. The endothecial cells are large and develop fibrous thickenings. The microspore mother cell undergoes two successive reduction divisions, giving rise to isobilateral microspore tetrad. The tetrad separates and give rise to four pollen grains. Occasionally, the anther show degenerating pollen grains before dehiscence. Formation of Ubisch's bodies has also been observed. The pollen grains shed at three celled stage. The exine is thick while intine is thin. The ovule is anatropous, bitegmic and crassinucellate. The female archesporial cell becomes large with dense cytoplasm. It directly functions as megaspore mother cell and undergoes two meiotic divisions to produce a linear megaspore tetrad. The micropylar three cells degenerate and chalazal one becomes functional. The chalazal functional megaspore undergoes three mitotic divisions without wall formation and produces 8-nucleate embryosac. Such 8-nucleate embryosac organizes into Polygonum type of embryosac. It is interesting to note that some somatic cells of the ovule undergo nuclear divisions and give rise to facultative apomictic embryosacs. Key Words: Eldoret; Microsporangium; Ubisch's bodies; Facultative apomixis; Female gametophyte. DOI: 10.3126/sw.v7i7.3822 Scientific World Vol.7(7) 2009 pp.37-40


1990 ◽  
Vol 68 (2) ◽  
pp. 243-257 ◽  
Author(s):  
James W. Kimbrough ◽  
Jack L. Gibson

Cytological observations are made on apothecial tissues of Geopyxis carbonaria, using transmission electron microscopy. Characteristic features of both the medullary and ectal excipula are examined. Changes in ascus apex and wall structures are examined during ascus ontogeny, especially in relation to operculum position and structure. Ultrastructure of septum configuration is observed and compared in the excipulum, ascogenous hyphae, paraphyses, and at the base of young asci. Ascosporogenesis is observed from the ascus mother cell stage and initial spore delimitation until secondary wall formation. The cytological and ultrastructural observations on this species are discussed in relation to their possible taxonomic or phylogenetic value. Key words: ascosporogenesis, Discomycetes, ascospore ultrastructure, septal ultrastructure, cytochemistry.


2009 ◽  
Vol 55 (3) ◽  
pp. 227-234 ◽  
Author(s):  
Shanliang Xu ◽  
Danli Wang

Abstract To explore the life cycle of Craspedacusta, the authors collected male and female specimens of the Craspedacusta sowerbyi xinyangensis in a small fire-fighting pond in Ningbo, Zhejiang Province in July, 2005 and 2006. The development of C. sowerbyi xinyangensis was studied from zygote to medusa by means of light microscopy and digital camera. The zygotes of C. sowerbyi xinyangensis are globular and smooth (90 - 105 μm diameter) and have an equal, total cleavage to the two-cell stage 15 min after fertilization. The embryos enter the four-cell stage after another 15 min and become multicellular embryos after 3h 15 min. At this stage the embryos have a diameter similar to fertilized eggs but have uneven surfaces that are distinct from the smooth surfaces of the uncleaved zygotes. Solid gastrulae are formed 7 h after fertilization. These are spherical planulae with short surface cilia that begin to swim in slow clockwise circles. After 12 h, they lose their cilia, cease swimming and become elongated planulae with one end larger than the other. Rod-like planulae, similar in thickness at both ends, are formed after an additional 7 h. After 4 days, the planulae develop into tiny polyps having two germ layers and a gastrovascular cavity. The polyp mouth is 50 - 62 µm in diameter, lacking tentacles but having nematocysts around the mouth. Planulae become mature polyps after 10 days (15 days after fertilization). Medusa buds (45 - 88 μm diameter) are formed by polyp budding, which soon become free-living medusae with 8 tentacles (380 - 620 μm diameters). Sometimes, the movement of frustules, which are formed by the polyps and similar to planulae in morphology can also be observed.


1974 ◽  
Vol 52 (3) ◽  
pp. 435-441 ◽  
Author(s):  
Harry T. Horner Jr. ◽  
Milton A. Rogers

In the male-fertile line of pepper, microsporogenesis and pollen development are normal. During meiosis, the meiocytes become encased in callose and a locular cavity forms. A rudimentary pollen wall, preceded by primexine deposition, is formed at the tetrad stage around the microspores before their release from the callose. The tapetum remains peripheral in the locule until the vacuolate pollen stage when it disappears. The sporogenous cells of the cytoplasmic male-sterile line complete meiosis, and the callose-encased microspores also deposit a primexine. Further development of the microspores is arrested. Before and during meiosis the tapetal cells become highly vacuolate and remain appressed to the meiocytes; a locular cavity is not formed. After primexine deposition, the tetrads of microspores, which are still encased in callose, seem to collapse as they are encroached upon by the vacuolate tapetum. After abortion of the microspores the outer tapetal layer degenerates, followed by the inner tapetal layer. The aborted mass late in anther development consists of crushed microspore tetrads, primary walls of the sporogenous cells and tapetum, callose, and the collapsed tapetum. The manner of abortion in pepper is compared with previously described mechanisms.


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