An electron microscopic study of the formation and structure of the periostracum in Astarte (Bivalvia)

1974 ◽  
Vol 52 (12) ◽  
pp. 1463-1471 ◽  
Author(s):  
A. S. M. Saleuddin

An electron microscopic study of the outer and middle folds of the mantle edge of Astarte castanea reveals the fine-structural details of the cells which are involved in the formation of the periostracum. There are four types of cells in the outer fold whereas there is only one type in the middle fold. The role of different cell types in the formation of the periostracum has been discussed. The periostracum originates in the intercellular space between the basal cell of the outer fold and the first cell of the middle fold. Even at the point of origin it consists of two outer membranous layers and the inner dark homogeneous layer. The fibrous translucent layer, which is the third layer of the fully mature periostracum, does not appear until the young periostracum has moved down the periostracal groove at the level of the third cell. As the periostracum matures, the two membranous layers remain remarkably constant in width, whereas the two inner layers, dark homogeneous and fibrous translucent, increase in thickness. Scanning electron microscopy and thin sectioning reveal that the fully mature periostraca of A. castanea and A. elliptica appear uniformly pitted, but the nature of the pits between the two species is different. The fibrils of the fibrous layer show either uniform or random arrangements, depending on the region. It is the innermost part of the fibrous layer of the periostracum that provides the nuclei for calcification.

1968 ◽  
Vol 46 (5) ◽  
pp. 745-747 ◽  
Author(s):  
William W. L. Chang ◽  
Sergio A. Bencosme

A reevaluation of the silver methenamine reaction as an electron stain has ensued from recent use of glutaraldehyde fixation alone. By this technique, three cell types of rat adrenal medulla were found: (i) the norepinephrine-containing cells showed selectively stained, irregular, black granules; (ii) the epinephrine-containing cells showed round, light-grey granules; and (iii) the third cell type showed round granules like those of epinephrine-containing cells, but black in color, similar to those of the norepinephrine-containing cells.


1985 ◽  
Vol 24 (4) ◽  
pp. 457-462 ◽  
Author(s):  
Toshio Matsushima ◽  
Masashi Fukui ◽  
Katsutoshi Kitamura ◽  
Toru Soejima ◽  
Michiya Ohta ◽  
...  

1987 ◽  
Vol 65 (12) ◽  
pp. 2959-2968 ◽  
Author(s):  
Hameed Al-Hajj ◽  
Suha Janakat ◽  
Fahmi Mahmoud

Early differentiation of the spermatid of Agama stellio is demonstrated by two anterior nuclear depressions, occupied by two proacrosomal vesicles, which fuse to form one vesicle. Later, this vesicle exhibits an acrosomal granule in its midposterior portion. The space between the posterior acrosomal membrane and the nuclear envelope is occupied by a subacrosomal fibrous layer which later exhibits a subacrosomal granule posterior to the acrosomal granule. The acrosomal vesicle and the nuclear depression flatten and later elongate. The acrosomal granule spreads and assumes the inverted V shape of the acrosomal vesicle, and the subacrosomal material assumes a feathery shape capping the nuclear prolongation. The subacrosomal granule on top of this feathery material forms a long, cross-striated subacrosomal rod which extends towards the tip of the acrosome. The chromatin material undergoes condensation into spirally oriented fibers, which eventually become homogeneous and dense. This process is accompanied by a change in the orientation of the manchette microtubules, which initially occur as rings around the nucleus and are eventually found parallel to the longitudinal axis of the nucleus.


1986 ◽  
Vol 6 (4) ◽  
pp. 1148-1157 ◽  
Author(s):  
L D Saffer ◽  
O L Miller

An electron microscopic study was made of the replication of rDNA chromatin of Saccharomyces cerevisiae. Two different methods were used to synchronize cells. cdc7-1 cells were raised to a restrictive temperature, whereas A364a cells were blocked with mating factor. Replication bubbles typically opened in the nontranscribed spacers of rDNA repeats in both cell types. The mean position of the center of these bubbles corresponds closely to a position where an autonomously replicating sequence previously has been mapped in an rDNA repeat. Clusters of replication bubbles containing up to four bubbles spaced one to three genes apart were seen opening in early S phase.


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