, Volume 149, Issue 2, pp 245-266

Structure and fine structure of the hypophyseal pars distalis in endigenous African species of the genus Tilapia

Rent the article at a discount

Rent now

* Final gross prices may vary according to local VAT.

Get Access

Summary

The structure and fine structure of the pars distalis hypophyseos was examined in five species of Tilapia fishes (T. alcalica, T. grahami, T. leucosticta, T. zillii, T. nigra) which were collected from lakes of a wide range of salinities. The pars distalis in all the species is composed of 5 granulated (“secretory”) and 1 chromophobic cell types. The rostral pars distalis prolactin cells appear most numerous and active in the fresh water species and smaller and least active in the “soda” lake fish. The evidence from nuclear measurements suggests that the species adapted to hyposmotic media have compensated for the freshwater environment (and the subsequent need for greater prolactin secretion) by increasing the number of prolactin cells rather than by increasing the synthetic activity of individual cells.

In “soda” lake species which were acclimated to fresh water the prolactin cells are markedly hyperactive and degranulated when compared with any other group.

The ACTH cells appear more active in the “soda” lake species than in the fresh water groups, however, these cells are maximally active in “soda” lake fish acclimated to fresh water.

The rostral pars distalis stellate cells are described and discussed in relation to their possible involvement in the release of hormone from the pars distalis “secretory” cells.

The proximal pars distalis somatotrophs appear active in all the species investigated although they were maximally active in fresh water acclimated “soda” lake species. The structure of the proximal pars distalis gonadotrophs and thyrotrophs is variable both within the same animal and between the species but the variation is not consistent with environmental salinity parameters.

The means by which granules are released from the different cell types is discussed.

The work was supported by grants in aid of research from SRC (J.F.L), University of Nairobi (J. F. L. and M. H), NRC (J.F.L.), USPMS (AM 13795, J. N. B.), Munitarp Foundation (M. H.) and by a travel scholarship from the Royal Society (J.F.L.).

The paper is number 091 in the physiology of migration series.

We are indebted to Prof. J. G. Phillips for his support to one of us (J.F.L.) during part of the period of this work. We also wish to thank R. Lindsay, C. Cooper (J.F.L.), Miss S. Khan, M. Crighton, Mrs. A. Shah, Dr. J. Sale, Dr. C. Pennycuik (M. H. and J.F.L.) and Mrs. P. V. Gaitens (J.N.B.) for their help in collecting the fish and/or processing the tissues and D. Hollingworth (J.N.B.) and Mrs. L. Lin (J.F.L.) for their photographic assistance. We also offer our sincere thanks to the representatives of the Magadi Soda Company, the Sagana hatchery and Lake Nakuru National Park for the use of their facilities.