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Journal ArticleDOI

Structural evidence for two different testicular types in teleost fishes.

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TLDR
Testicular structure in Salmoniformes, perciform, and cypriniform teleosts studied has been examined and reinterpreted on the basis of two different tubular types, distinguished from each other by the intratubular distribution of spermatogonia.
Abstract
Testicular structure in Salmoniformes, Perciformes, Cypriniformes, and Atheriniformes has been examined and reinterpreted on the basis of two different tubular types, distinguished from each other by the intratubular distribution of spermatogonia. In the salmoniform, perciform, and cypriniform teleosts studied, spermatogonia are distributed along the entire length of the testicular tubules. However, in the atheriniform teleosts spermatogonia are restricted to the distal end of the tubule. Sperm development in teleosts is cystic, cysts being comprised of Sertoli-cell processes. In both testicular types described, Sertoli cells phagocytize spermatid residual bodies. Together witb the germ cells, they comprise the only intratubular cell types within the teleostean testis. Boundary cells are located immediately outside of the tubule basement membrane. They do not form a complete layer over the tubule surface; therefore, interstitial Leydig cells and blood vessels may border directly upon the tubular basement membrane.

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6 The Functional Morphology of Teleost Gonads

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Spermatogenesis and spermatology of some teleost fish species

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References
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Journal ArticleDOI

Further Observations on the Blood-Testis Barrier in Monkeys

TL;DR: Electron-opaque tracer studies demonstrate that the initiation of meiosis occurs while the early spermatocytes are still in the basal compartment of the epitheium and may not require the special microenvironment provided by the Sertoli cells in the adluminal compartment.
Journal ArticleDOI

Functional Morphology of the Testis

TL;DR: These sections were used to identify the stages of the cycle of the seminiferous epithelium in the monkey as described by Clermont (1969), and the techniques utilizing intercellular tracer compounds such as lan- thanum nitrate and horseradish peroxidase have been described previously.
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