A rationale is presented for a primary nursing strategy and an on-growing strategy for Clarias gariepinus (Burchell) culture in Africa, thus providing a potential model for the development of culture technology for the species. Existing information pertaining to the production strategies identified is reviewed, highlighting the attributes of African catfish for aquaculture. Some of the current deficiencies and inconsistencies in available information pertaining to controlled hatchery production are addressed. The early developmental stages of Clarias gariepinus are defined, in order to promote consistent use of terminology and help farmers better address the changing needs of their developing stock. The pattern of growth and survival of larvae and fry is investigated at higher stocking densities than those used experimentally to provide a database for planning full-scale commercial operations. Tank design and water flow rates appropriate for Clarias gariepinus in hatcheries are investigated and recommendations made. Finally, in order to promote maximal growth rates of hatchery stocks the maximum daily feed intake of larvae in relation to different feeding regimes is estimated based on rates of gastric evacuation and return of appetite. An overview of the controlled hatchery production of Clarias gariepinus is presented.

Thesis (M.S.)--Virginia Polytechnic Institute and State University, 1994. / Vita. Abstract. Includes bibliographical references (leaves 80-88). Also available via the Internet.

Thesis (M.S.)--Auburn University, 2008. / Abstract. Vita. Includes bibliographical references (p. 62-75).

Thesis (Ph. D.)--University of Chicago, 1914. / "Reprinted from the Journal of comparative neurology and psychology, volume 20, no. 4, 1910." Bibliography: p. 389-392.

This thesis represents a detailed investigation into aspects of the biology, ecology and population dynamics of two endemic ariid species, Galeichthys feliceps and G. ater, off the southeast coast of South Africa. The two species are exploited as a by-catch in the commercial ski-boat fishery off Port Alfred, a fishery dominated by highly fecund sparid and sciaenid species. They collectively constitute approximately 10% of the total annual catch in terms of landed mass G. feliceps outnumber G. ater in the catches by a ratio of 3:1. The investigation was designed to provide the biological data required for stock assessment and to determine optimum management strategies for the two populations. The implications of their K-selected life-history styles for exploitation received particular attention. While the two species were sympatric and had similar depth distributions they were found to be allopatric with respect to their foraging habitats. G. feliceps foraged over sandy and muddy substrata in marine and estuarine environments. G. ater fed only on reef-associated species and did not utilise estuaries. Their feeding-associated morphologies were identical and both species preyed primarily on crustaceans (brachyuran crabs and isopods), echiurids, molluscs and polychaetes. The diet of G. ater was broader in terms of the number of species consumed. The two species are mouth-brooders with low fecundity. G. feliceps and G. ater produced a mean of 49 and 32 eggs each, per annum. The buccal incubation period was determined to be in the region of 140 days for G. feliceps. Embryos hatched after approximately 75-80 days and the young began exogenous feeding thereafter. The young fed intra-buccally on detritus provided by the parent. Adult buccal mucus may also have been used as a food source. Young were released at a total length of ± 55mm. Adult males ceased feeding whilst mouth-brooding. Body musculature, abdominal fat and liver reserves provided energy for basal metabolism and males lost approximately 28% of their body mass during buccal incubation. Females expended less reproductive energy than males. Catches were dominated by mature fish (76% in G. feliceps and 97% in G. ater). Females were significantly more abundant in catches during the spawning and mouth-brooding period. The female to male sex ratios were 1.65:1 and 2.23:1 for G. feliceps and G. ater respectively. Age and growth studies revealed that the two species mature at advanced ages (10 and 9 years for G. feliceps and 9 and 7 years for G. ater males and females respectively). They are long-lived, reaching ages in excess of 18 years in G. feliceps and in excess of 15 years in G. ater. Females live longer than males and grow larger. Yield-per-recruit and spawner biomass-per-recruit analyses demonstrated that G. ater were exploited below FO.1 at a level where spawner biomass-per-recruit was reduced to between 45% and 65% of the unexploited level. The G. ater stock was not adversely affected by current levels of fishing effort. For G. feliceps, both sexes were exploited beyond F₀.₁ where spawner biomass-per-recruit was reduced to between 30% and 22% of the unexploited level. G. feliceps were shown to be sensitive to relatively low levels of exploitation, a phenomenon attributed to their highly Kselected life-history style. Should the species become targeted for in the future, effort restrictions in the form of a closed season during the spawning and mouth-brooding period would prove effective in reducing effort and conserving the population sex ratio.

A description is given of the location, anatomy and morphology of the endocrine glands likely to be involved in controlling the reproductive cycle of C. gariepinus. Methods of identifying the secretory tissues in the light and electron microscopes are outlined. A review of the published results on homologous tissues from other teleosts is included and directions for further research on the endocrinology of C. gariepinus are discussed.

No description available.

The need for developing an artificial dry feed for Clarias gariepinus larvae was identified. Dry larval fishfeed requires certain physical properties. Techniques for manufacturing feeds which comply with these requirements were evolved and are recomended for practical use. The techniques that were used for artificial reproduction of C. gariepinus larvae are briefly discussed. The larvae were fed on various dietary formulations and their growth responses were monitored in order to determine their nutritional requirements. A feed was developed which gave superior results to those obtained with natural food organisms. This feed consisted of Torula yeast(69,8%), fishmeal(23,3%), vitamin supplements(O,9%), methionine supplement (150mg/kg), bactericide and preservatives. The feed particles were coated with a lipid supplement which was added at a ratio of 6% to the weight of the feed. The optimum particle size (diameter) for C. gariepinus larvae is 2,2% of their mean total length. The larvae should be given a feed ration of 25% of body weight per day at a frequency of once every four hours. A favourable feed conversion ratio of 1.1g of feed consumed per gram of larval weight gain was experienced. The established dry feed is suitable for use in commercial hatcheries and can be used as a standard and proven food source for further research on the intensive rearing of C. gariepinus larvae.

Corydoras aeneus is an armoured catfish found in the upper amazon regions of South America. It is a member of the family Callichthyidae. Studies done with this species of fish showed that C. aeneus is a tetraploid with a chromosome number of 132 (Scheel et al. , 1972). Dunham et al. (1980) reported 120 chromosomes. The C. aeneus used in this study were bought from direct importers. We had four samples of fishes supposedly coming from Brazil (Belem), Guyana, Peru and Trinidad. During our initial studies in an attempt to karyotype aeneus we came across individuals with a highly reduced chromosome number. A diploid form of C. aeneus was discovered. Only those fishes from our Belem sample were diploid. A comparison of the diploid and tetraploid forms was done. Both forms were karyotyped, the tetraploid form of C. aeneus has 134 chromosomes and the diploid has 56. Physically both forms looked exactly the same. Morphometric as well as meristic data was collected from 131 fishes and analyzed by multivariate, discriminant and contingency chi- square analyses. The results obtained do not suggest any absolute morphological differences between the diploid and the tetraploid forms anymore than between tetraploids. / M.S.

Typescript (photocopy). / Digitized by Kansas Correctional Industries