Studies on the fresh water fairy shrimpChirocephalopsis bundyi (Forbes). II. Histochemistry of egg-shell formation

1960 ◽  
Vol 107 (3) ◽  
pp. 259-283 ◽  
Author(s):  
Harris J. Linder
1971 ◽  
Vol 50 (2) ◽  
pp. 577-580 ◽  
Author(s):  
R.D. Creek ◽  
Pauline Lund ◽  
O.P. Thomas ◽  
W.O. Pollard

1991 ◽  
Vol 32 (4) ◽  
pp. 853-864 ◽  
Author(s):  
A. L. Waddell ◽  
R. G. Board ◽  
V. D. Scott ◽  
S. G. Tullett

Science ◽  
1945 ◽  
Vol 101 (2633) ◽  
pp. 617-618 ◽  
Author(s):  
R. BERNARD ◽  
P. GENEST

Parasitology ◽  
1964 ◽  
Vol 54 (4) ◽  
pp. 699-719 ◽  
Author(s):  
A. O. Anya

The histological anatomy of the female reproductive system of an oxyuroid nematode,Aspiculuris tetraptera, Schulz, has been described.The process of egg-shell formation in this animal has been followed in detail while the structural and chemical characteristics of the egg-shell have been studied by histochemical and other methods. It is shown that there are three layers: a lipoprotein layer, a ‘chitinous’ layer and the so-called vitelline (glycosidal) membrane. Evidence is presented for the exogenous origin of the lipoprotein layer: this being formed by the cells of the upper uterus which are shown to be secretory.The question of quinone-tanning in the egg-shell ofA. tetrapteraand in other oxyuroids and ascarids is considered. It is shown that neither a polyphenol oxidase nor a high concentration of phenolic substances (apart from protein tyrosine) exists in this system. The significance of these and other observations is discussed in relation to the mechanism of tanning as elucidated in insects and trematodes.I have to acknowledge with gratitude the support of many during these investigations. To Dr P. Tate for his encouragement and provision of facilities at the Molteno Institute; to Dr D. L. Lee, for much useful discussion and permission to refer to some of his unpublished electron micrographs of nematodes; to Professor J. D. Smyth, who kindly read through the manuscript; to the Cambridge Philosophical Society for a grant that made possible the translation of Fauré-Frémiet's classical study onAscaris;and to the Department of Technical Cooperation for financial assistance.


1969 ◽  
Vol 111 (5) ◽  
pp. 647-652 ◽  
Author(s):  
K. Simkiss

The intracellular pH of the shell gland of the domestic fowl was calculated at various stages in egg-shell formation. The calculation is based on the distribution of 5,5-dimethyloxazolidine-2,4-dione between intracellular and extracellular water. The results show a rapid fall in intracellular pH at the time of mineralization and this is interpreted as indicating a removal of protons from the site of calcification.


Parasitology ◽  
1976 ◽  
Vol 72 (1) ◽  
pp. 29-39 ◽  
Author(s):  
Michael A. McClure ◽  
A. F. Bird

SummaryOogonia of Meloidogyne javanica are radially arranged around a central rachis to which they are attached by cytoplasmic bridges. As the oocytes mature the rachis disappears and the oocytes pass through the oviduct in tandem. The oviduct-spermatotheca valve is constructed of two rows of tightly packed cells of which there are four per row. The nuclei of these cells are large and contain balloon-shaped cytoplasmic invaginations. The spermatotheca is characterized by microtubules which extend to its lumen and by invaginations of plasmalemma. Cells of the distal uterine region contain large intracytoplasmic spaces bordered by endoplasmic reticulum whereas proximal uterine cells have dense cytoplasm and large areas of compact endoplasmic reticulum. Egg-shell formation begins in the spermatotheca with the modification of the oolemma to form the vitelline layer. The chitinous layer begins in the distal portion of the uterus and appears to originate from the egg. Proline-containing protein is incorporated into the chitinous and lipid layers as the egg passes through the mid-region of the uterus and formation of the lipid layer in this region completes egg development.


Parasitology ◽  
1979 ◽  
Vol 78 (2) ◽  
pp. 131-143 ◽  
Author(s):  
D. A. Wharton

SUMMARYThe ovary of Aspiculuris tetraptera has a prominent terminal cap cell. This is considered to be part of the ovarian epithelium. Oogonia detach from the short rachis and increase in size from 6 to 60 μm; accumulating hyaline granules, shell granules and glycogen. The hyaline granules persist in the egg cytoplasm after shell formation has been completed and are considered to be lipoprotein yolk. The shell granules contribute to the non-chitin fraction of the chitinous layer. A classification of the cytoplasmic inclusions of the nematode oocyte is proposed. Upon fertilization a vitelline membrane is formed which constitutes the vitelline layer of the egg-shell. The chitinous layer is secreted in the perivitelline space, between the vitelline layer and the egg oolemma. Upon completion of chitinous layer synthesis, the egg cytoplasm contracts away from its inner surface. The material of the lipid layer is secreted at the surface of the egg cytoplasm and adheres to the inner surface of the chitinous layer. During secretion of the chitinous and lipid layers by the egg cytoplasm, the uterine cells secrete the unit membrane-like external uterine layer and the crystalline internal uterine layer. A complex system of interconnecting spaces develops in the internal uterine layer. This system is open to the exterior via breaks in the external uterine layer. There is no direct involvement of the uterine cells in the formation of this structure.


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