Anatomy of the Unpollinated and Pollinated Watermelon Stigma

1982 ◽  
Vol 54 (1) ◽  
pp. 341-355
Author(s):  
M. SEDGLEY

The structure of the watermelon stigma before and after pollination was studied using light and electron microscopy, freeze-fracture and autoradiography. The wall thickenings of the papilla transfer cells contained callose and their presence prior to pollination was confirmed using EM-autoradiography, freeze-fracture and fixation. No further callose thickenings were produced following pollination. Pollination resulted in a rapid increase in aqueous stigma secretion and localized disruption of the cuticle, which appeared to remain on the surface of the secretion. Autolysis of the papilla cells, which had commenced prior to pollination, was accelerated and appeared to take place via cup-shaped vacuoles developed from distended endoplasmic reticulum. The reaction was localized to the papilla cells adjacent to the pollen tube only. Both pollen-grain wall and stigma secretion contained proteins, carbohydrates, acidic polysaccharides, lipids and phenolics.

1975 ◽  
Vol 18 (1) ◽  
pp. 1-17
Author(s):  
A. Pleshkewych ◽  
L. Levine

A prominent cytoplasmic inclusion present in living mouse primary spermatocytes has been observed by both light and electron microscopy. It began to form at prometaphase and continued to increase in thickness and length as the cells developed. By metaphase it was a distinct sausage-shaped boundary that enclosed a portion of the cytoplasm between the spindle and the cell membrane. At the end of metaphase, the inclusion reached its maximum length. At telophase, it was divided between the daughter secondaries. The inclusion persisted as a circular contour in the interphase secondary spermatocyte. Electron microscopy of the same cultured cells that were previously observed with light microscopy revealed that the inclusion was a distinctive formation of membranes. It consisted of agranular cisternae and vesicles, and was therefore a membranous complex. Many of the smaller vesicles in the membranous complex resembled those found in the spindle. The cisternae in the membranous complex were identical to the cisternal endoplasmic reticulum of interphase primary spermatocytes. Nevertheless, the organization of vesicles and cisternae into the membranous complex was unique for the primaries in division stages, since such an organization was not present in their interphase stages.


2012 ◽  
Vol 2012 ◽  
pp. 1-8 ◽  
Author(s):  
M. Gotelli ◽  
B. Galati ◽  
D. Medan

Tapetum, orbicule, and pollen grain ontogeny inColletia paradoxaandDiscaria americanawere studied with transmission electron microscopy (TEM). The ultrastructural changes observed during the different stages of development in the tapetal cells and related to orbicule and pollen grain formation are described. The proorbicules have the appearance of lipid globule, and their formation is related to the endoplasmic reticulum of rough type (ERr). This is the first report on the presence of orbicules in the family Rhamnaceae. Pollen grains are shed at the bicellular stage.


1981 ◽  
Vol 59 (5) ◽  
pp. 908-928 ◽  
Author(s):  
Martha J. Powell ◽  
Charles E. Bracker ◽  
David J. Sternshein

The cytological events involved in the transformation of vegetative hyphae of the zygomycete Gilbertella persicaria (Eddy) Hesseltine into chlamydospores were studied with light and electron microscopy. Thirty hours after sporangiospores were inoculated into YPG broth, swellings appeared along the aseptate hyphae. Later, septa, traversed by plasmodesmata, delimited each end of the hyphal swellings and compartmentalized these hyphal regions as they differentiated into chlamydospores. Nonswollen regions adjacent to chlamydospores remained as isthmuses. Two additional wall layers appeared within the vegetative wall of the developing chlamydospores. An alveolate, electron-dense wall formed first, and then an electron-transparent layer containing concentrically oriented fibers formed between this layer and the plasma membrane. Rather than a mere condensation of cytoplasm, development and maturation of the multinucleate chlamydospores involved extensive cytoplasmic changes such as an increase in reserve products, lipid and glycogen, an increase and then disappearance of vacuoles, and the breakdown of many mitochondria. Underlying the plasma membrane during chlamydospore wall formation were endoplasmic reticulum, multivesicular bodies, vesicles with fibrillar contents, vesicles with electron-transparent contents, and cisternal rings containing the Golgi apparatus marker enzyme, thiamine pyrophosphatase. Acid phosphatase activity was localized cytochemically in a cisterna which enclosed mitochondria and in vacuoles which contained membrane fragments. Tightly packed membrane whorls and single membrane bounded sacs with finely granular matrices surrounding vacuoles were unique during chlamydospore development. Microbodies were rare in the mature chlamydospore, but endoplasmic reticulum was closely associated with lipid globules. As chlamydospores developed, the cytoplasm in the isthmus became highly vacuolated, lipid globules were closely associated with vacuoles, mitochondria were broken down in vacuoles, unusual membrane configurations appeared, and eventually the membranes degenerated. Unlike chlamydospores, walls of the isthmus did not thicken, but irregularly shaped appositions containing numerous channels formed at intervals on the inside of these walls. The pattern of cytoplasmic transformations during chlamydospore development is similar to events leading to the formation of zygospores and sporangiospores.


1969 ◽  
Vol 17 (7) ◽  
pp. 454-466 ◽  
Author(s):  
EDWARD ESSNER

The peroxidase activity of microbodies in fetal mouse liver was studied by light and electron microscopy. Two types of microbodies were present; a small population of bodies that lacked a nucleoid, predominant on the 16th day of gestation, and a larger population of nucleoid-bearing microbodies, predominant on the 19th day, in association with the rough endoplasmic reticulum from which they probably originate. Both types of bodies were visualized when incubated for peroxidase activity but were negative (19th day) for acid phosphatase activity. The findings suggest that the anucleoid- and nucleoid-bearing organelles together constitute the microbody population of the fetal liver.


1973 ◽  
Vol 51 (12) ◽  
pp. 2307-2314 ◽  
Author(s):  
Saeed R. Khan ◽  
Henry C. Aldrich

Termitaria snyderi Thaxter forms small discoid lesions on the exoskeleton of different species of termites. Its conidiogenesis has been studied by light and electron microscopy. The phialides are oriented parallel in a closely packed sporodochium. The conidia are produced endogenously in basipetal succession from a fixed conidiogenous locus and are liberated when the tip is broken off the phialide as a result of the force applied by the formation of new conidia. The area of the phialide beyond the locus forms a tubular collarette. The conidium initial buds out at the locus and after it has received its organelles and reached a certain size it is delimited by a centripetally growing transverse septum. The region of the growing septum has many vesicles which may be involved in cross wall synthesis. Conidia are cylindrical, uninucleate, and double-walled. They have mitochondria, endoplasmic reticulum (ER), conspicuous lipid droplets, and vacuoles. Each conidiophore has long mitochondria, elongate nuclei, and much endoplasmic reticulum. The plasmalemma of the conidiophore is highly convoluted.


1987 ◽  
Vol 105 (4) ◽  
pp. 1649-1662 ◽  
Author(s):  
L Sperling ◽  
A Tardieu ◽  
T Gulik-Krzywicki

Paramecium trichocysts are unusual secretory organelles in that: (a) their crystalline contents are built up from a family of low molecular mass acidic proteins; (b) they have a precise, genetically determined shape; and (c) the crystalline trichocyst contents expand rapidly upon exocytosis to give a second, extracellular form which is also an ordered array. We report here the first step of our study of trichocyst structure. We have used a combination of x-ray powder diffraction, freeze-etching, and freeze-fracture electron microscopy of isolated, untreated trichocysts, and density measurements to show that trichocyst contents are indeed protein crystals and to determine the elementary unit cell of both the compact intracellular and the extended extracellular form.


1990 ◽  
Vol 68 (7) ◽  
pp. 1454-1467 ◽  
Author(s):  
K. M. Fry ◽  
S. B. McIver

Light and electron microscopy were used to observe development of the lateral palatal brush in Aedes aegypti (L.) larvae. Development was sampled at 4-h intervals from second- to third-instar ecdyses. Immediately after second-instar ecdysis, the epidermis apolyses from newly deposited cuticle in the lateral palatal pennicular area to form an extensive extracellular cavity into which the fourth-instar lateral palatal brush filaments grow as cytoplasmic extensions. On reaching their final length, the filaments deposit cuticulin, inner epicuticle, and procuticle sequentially on their outer surfaces. The lateral palatal crossbars, on which the lateral palatal brush filaments insert, form after filament development is complete. At the beginning of development, the organelles involved in plasma membrane and cuticle production are located at the base and middle of the cells. As the filament rudiments grow, most rough endoplasmic reticulum, mitochondria, and Golgi apparatus move to the apex of the epidermal cells and into the filament rudiments. After formation of the lateral palatal brush filaments and lateral palatal crossbars, extensive organelle breakdown occurs. Lateral palatal brush formation is unusual in that no digestion and resorption of old endocuticle occurs prior to deposition of new cuticle. No mucopolysaccharide secretion by the lateral palatal brush epidermis was observed, nor were muscle fibres observed to attach to the lateral palatal crossbars, as has been suggested by other workers.


1990 ◽  
Vol 68 (11) ◽  
pp. 2509-2516 ◽  
Author(s):  
Gamal A. El-Ghazaly ◽  
William A. Jensen

Light and electron microscopy studies show that pollen wall development in plants treated with the gametocide RH0007 and untreated plants was similar until the stage at which sporopollenin is normally deposited on the wall. At this stage, the pollen wall of treated plants is 80% thinner than that of the control. Shortly after this stage, the pollen grains in the treated plants collapse and abort. We conclude that the gametocide clearly acts through the inhibition of sporopollenin formation, which results in pollen death. As sporopollenin is found only in the pollen wall of seed plants and the spores of nonseed plants, harm to other parts of the plant is not expected to occur. Key words: pollen wall development, Triticum aestivum, gametocide.


1983 ◽  
Vol 61 (10) ◽  
pp. 2515-2526 ◽  
Author(s):  
Fred D. Sack ◽  
D. J. Paolillo Jr.

Key protoplasmic features of stomatal development in Funaria hygrometrica Hedw. (Musci) were characterized using light and electron microscopy. Endoplasmic reticulum (ER) cisternae are initially rough and often arranged in parallel arrays. During pore formation, the cytoplasm becomes packed with tubular, smooth ER. Older but still functional stomata contain small amounts of primarily cisternal ER. Lipid bodies decrease in electron density when tubular ER appears. Preliminary observations indicate that two large vacuoles occupy the polar regions of open, but not closed, stomata. Intact plasmodesmata occur in developing but not mature walls. Plastid structure, microtubule distribution, and other protoplasmic features are essentially similar to those described in the stomata of other genera.


1975 ◽  
Vol 53 (24) ◽  
pp. 2958-2977 ◽  
Author(s):  
Jack Maze ◽  
Shu-Chang Lin

In Stipa elmeri Piper & Brodie ex Scribn., the pollen tube enters at the filiform apparatus of the degenerated synergid. The degenerated synergid has electron-dense cytoplasm in which organelles are not discernible. All other cells of the mature megagametophyte have nuclei, endoplasmic reticulum, plastids, mitochondria, dictyosomes, and vacuoles. Starch is found in the persistent synergid (in minute quantities), egg, and central cell. Lipids occur in the persistent synergid, central cell, and antipodals. The filiform apparatuses of the two synergids are hypothesized to perform different functions. In the degenerated synergid, the filiform apparatus serves to increase the surface area of the plasma membrane and thereby to offer a large area for pollen-tube-growth-directing compounds to diffuse out of the synergid. In the persistent synergid, the filiform apparatus is part of a suite of features which indicate that the persistent synergid is involved in the transference of materials into the megagametophyte. Another possible function of the persistent synergid is to aid in establishing the polarity of the egg. The pollen grain and tube have distinctive polysaccharide spheres that serve to delimit the pollen tube cytoplasm after discharge into the degenerated synergid. Associated with the degenerated synergid are bodies of dense materials as seen under electron microscopy, and bodies of RNA and protein as determined histochemically. These are probably the same thing and come from the degenerating synergid. The antipodals are the most cytologically active cells of the megagametophyte. They have some features which are characteristic of transfer cells and possibly function in the transference of materials into the megagametophyte. Other studies (Brink and Cooper 1944) have indicated that grass antipodals are involved in the control of endosperm development. The active cytoplasm of the antipodals may reflect the synthesis or transference of growth-controlling substances.


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