Thesis (Ph.D.)--McMaster University, 2006. / Supervisor: Sigal Balshine. Includes bibliographical references (p. 183-199).

Thesis (Ph. D.)--University of Hong Kong, 1970. / Also available in print.

Thesis (doctoral)--University of Stockholm, 1983. / Includes bibliographical references.

Thesis (Ph. D.)--University of Wisconsin--Madison, 1973. / Typescript. Vita. eContent provider-neutral record in process. Description based on print version record. Includes bibliographical references.

An account is given of some aspects of the biology of Tilapia mossambica Peters in Lake Sibaya, South Africa. Previous work on Tilapia in Lake Sibaya is reviewed. Apart from brief gillnet surveys, which recorded the species' presence, no research on T. mossambica had been performed at Lake Sibaya before the two-year study of Minshull who collected data on food preferences, depth distribution of juveniles and breeding biology of adults. The main physiographical features of the lake are outlined. Lake Sibaya is a warm shallow coastal lake with extensive shallow terraces in the littoral which shelve abruptly into underwater valleys. The substrate is predominantly sandy. Aquatic macrophytes are generally restricted to water 1-7 m deep. Adult fishes (over 8 cm SL) are usually absent from water deeper than 12 m and shallower than 0.5 m, whereas juveniles may occur at all depths, and fry only in very shallow water. T. mossambica inhabits the littoral in the warm and transition periods (August to April) but moves into deep water in the cool season (May to July). Exposed and sheltered shallow areas are utilised for different purposes by adult fishes, the former for nesting, and the latter for feeding and mouth-brooding. Habitat selection by males was governed by nest site selection. Habitat Nests were most common in sheltered, sparsely vegetated littoral and sublittoral areas, but also present in well-vegetated sheltered areas. Breeding females preferred sheltered littoral areas but ventured onto the terrace to release the young. Juvenile and fry T. mossambica inhabited shallow exposed shores with a temperature gradient which reversed diurnally. The breeding, shoaling and feeding behaviour of T. mossambica is described, and integrated with data on T. mossambica from other systems. The breeding season spans seven months. Shoaling takes place in shallow water probably as a means of protection. T. mossambica is an omnivorous feeder relying largely on diatoms. The main predator is probably the barbel Clarias gariepinus, but avian predators may be more important. A method whereby the time of formation of rings on the scales of T. mossambica is described. The fishes were found to reach maturity after one year at a length of about 8 cm in females, and after two years at 10 cm in males. The breeding population had a standard length mode of 14 cm (females) and 17 cm (males). The maximum final size was about 24 cm SL. An estimate of the standing crop for fishes in the littoral and subiittoral areas of the eastern and southern shores of the south basin is given. The data were derived from a mark and recapture The biology of T. mossambica in Lake Sibaya as revealed by the present study is discussed with reference to data on the same and similar species in other systems. The utilis ation of the available resources in the lake by T. mossambica is commented upon, and reference is made to the significance of stunting, and the import ance of the retention of generalised characters for the successful habitation of the cyclically-renewed habitat of the littoral. Precocious breeding in T. mossambica is regarded as a functional adaptation which increases the proportion of fishes small enough to utilise the rich food resources in shallow water.

Using an experimental pressure chamber the rates of descent and the maximum depths of buoyancy equilibrium of some cichlid fishes were tested. Tilapia mossambica juveniles could descend to depths greater than 30 metres very rapidly. At 22°C small sub adult male fish (length ± 160 mm) could descend to a maximum buoyancy depth of 20 metres, small sub adult females to 13 metres while large adults (length ± 200 mm) of both sexes could descend to 11 metres. The fish generally take 4 to 5 days to reach their maximum equilibration depth. At 30°C mature adult male and female T.mossambica increased their maximum equilibration depth to 20 metres and at 15°C showed a decrease to a maximum depth of 6.7 metres. Temperature affects the rates of descent in a similar manner. T.rendalli can descend to 7.5 metres at 22°C. T.sparmanii can descend to 15 metres at 22°C. Hemihaplochromis philander fry and young juveniles are not affected by pressure. Adult males can descend to 16 metres at 22°C and 20 metres at 30°C. Adult females can descend to 26 metres at 22°C and 27 metres at 30°C. In T.mossambica oxygen appears to be the only gas secreted into the swimbladder to compensate for buoyancy loss. The haemoglobin of T.mossambica showed a marked Bohr and Root effect. Increased rates of descent with increased temperature are believed to be due to increased O₂ uptake, heart output etc. rather than as a direct effect of blood chemistry. The swimbladder wall of T.mossambica is extremely thin (2.8 ∕∪ m) and consequently a large amount of gas is lost through passive diffusion. Diffusion is not affected by temperature, consequently the increased secretory rates at higher temperatures are not balanced by a proportionately higher diffusion loss, thus enabling the fish to maintain a deeper buoyancy equilibrium at higher temperatures. Summary, p. 62-63.

The importance of the cichlid teleost Tilapia mossambica as a protein source, coupled with its remarkable adaptability, has resulted in its introduction into many water systems throughout the tropical, sub-tropical and even temperate regions of the world. However, its successful exploitation of these waters is dependent very largely upon the value of minimum temperatures and their duration. For e.g. Long et al (1961) has drawn attention to the tremendous mortalities of T. mossambica that occur in shallow water bodies during the precipitous temperature decreases that accompany the winter monsoons in Vietnam and other eastern countries, even at temperatures as high as 14 or 16º C. Coehe (1967) does not recommend stocking with T. mossambica where temperatures are not above 14º C all the time. Ailanson et al (1962) conclude, after an experimental study, that low temperatures (13º C or lower) in South African highveld dams in winter are certainly an important factor in the extensive mortalities of T. mossambica that have been reported from these dams. Jubb (1961) also reports that this species is often killed during a severe winter in Rhodesia. Intro., p.1.

The need for developing a dry feed which satisfied the nutrient requirements of Oreochromis mossambicus fry was identified. The spawning and grading techniques which resulted in a higher fecundity and ensured uniformity within and between samples of fry are discussed. Preparation techniques were developed which met the physical requirements of fry feeds. An analysis of the flesh and yolk sac fry for amino acid composition was undertaken. The initial test diet was based on these results, as well as on the natural feeding ecology of the species. Feeding trials were undertaken and growth responses monitored to determine the optimum levels of the various dietary components. A feed was developed which gave superior growth to that obtained with natural food organisms. This feed consisted of Torula yeast (47%), Weider Super Protein (44.39%), Vitamin supplement (0.45% - multivitamin), additional vitamin C supplement (0.16%), Spirulina (5%), and methionine supplement (3%). An optimum particle size range for O. mossambicus fry (between 5 & 25mm) was established at 125-200um. The fry should be fed the following feed ratios depending on age: 30.4% body weight/day up to day 5, 30.6% body weight/day up to day 10 and 25.1% body weight/day up to day 15. An optimum feeding frequency of 8/10hr day was recommended. A feed conversion ratio of 1.24:1 and a protein efficiency ratio of 0.682:1 was obtained. Digestable energy of the feed was determined at 16.1 kj/g feed. The established dry feed is suitable for use in commercial hatcheries, and as a formulation for further research on the intensive rearing of O. mossambicus fry.

The purpose of this thesis is to investigate the taxonomic status of Simochromis and Tropheue. Material for the study wae collected during three visits to Lake Tanganyika in 1976-1977. Tropheus polli G. S . Axelrod 1977, was found and described, and a new species of Simochromis was found and will be described in a forthcoming paper. Nine colour varieties of Tropheus maorii and three colour varieties of Tropheus duboisi were found and described. A diagnosis and description, with colour photographs, is given using morphometries and meristics of the five species of Simochromis and four species of Tropheus. A dissection and cleaning technique tor the pharyngeal apophysis and lower pharyngeal bone is explained, together with a method for the interpretation of relative bone composition of the pharyngeal apophysis. Photographs are included. The dentition is examined, evaluated and figured. Doubt has been cast upon the taxonomic validity of the composition of the pharyngeal apophysis as an indicator of affinity at the sub familial level. This is shown by its seeming lack of functional relationship, apparent arbitrary variation, interspecific variability in Simochromis and Tropheus, and intraspecific variability in S. diagramma and T. duboisi. Thus, the apophysis cannot be considered a reliable cichlid taxonomic characteristic at any level of classification, unless its validity is Substantiated in each instance. Furthermore, it is considered very probable that the Tropheus-Simochromis species complex is a monophyletic assemblage at the genus level, on the basis of similar dentition and mouth form, which is unique in Lake Tanganyika. It is proposed on phyletic grounds that Simochromis and Tropheus be united into the one genus Tropheus, and that Tropheus be divided into the subgenera , Tropheus (Tropheus) and Tropheus (Simochromis), along the lines of its previous division in two separate genera. Characteristics supporting this division include differences in the anal and dorsal fin meristic counts noted in the original descriptions of the genera. In addition, two modifications of the dentition were found during the course of this study which are not mentioned in any previous literature. It is considered probable, that Tropheus (Tropheus) and Tropheus (Simochromis) are monophyletic sister groups within the Tropheus complex. Pseudosimochromis Nelissen 1977 is not considered to be a taxonomically valid genus on either phyletic or gradistic grounds, and is included within Tropheus (Simochromis). The lower pharyngeal bone of T . (S.) diagramma is considered to be plesiomorphic in tooth arrangement, size and shape. A preliminary worKing hypothesis is established on the basis of the conjectures made and other available information which supports the phyletic relationship suggested by Fryer and lIes (1972). An illustration is given.

The nominal species Petrotilapia tridentiger Trewavas, a rock-frequenting fish from Lake Malawi, occurs in three distinct male and female colour forms at Monkey Bay. Field observations on courtship and aggression indicate that the three colour forms are distinct species. The taxonomy of the three species of Petrotilapia that occur at Monkey Bay is revised. R. tridentiger is redescribed and two new species, P. genalutea and P. nigra, are described. The three species are very similar morphologically and are considered to be sibling species. The only morphological character which reliably separates the three sibling species is live coloration: Live coloration is considered to be an important component of the specific mate recognition systems in Petrotilapia species. The coloration of a further fourteen forms of Petrotilapia is described and it is suggested that these forms are valid species. Space resource partitioning plays an important role in facilitating the coexistence of Petrotilapia sibling species. Space is partially partitioned in terms of depth range. In shallow water, where all three species are sympatric, there are differences in the feeding sites used by the various Petrotilapia forms. Changes in niche breadth and overlap, which are associated with changes in the abundance of epilithic algae, indicate that competition for feeding space occurs between the three Petrotilapia species. The Petrotilapia species partition their resources according to a social dominance hierarchy. Dominant forms, such as territorial males, R. tridentiger females and schooling R. genalutea females, have access to rich food supplies which occur within the territories of certain highly aggressive Pseudotronheus species. are facultative and opportunistic .feeders. Petrotilapia species Speciation in allopatry is considered to be the mechanism which adequately explains the current diversity of the genus Petrotilapia. The importance of an integrative approach to future systematic and ecological research on Lake Malawi cichlids is stressed. / KMBT_363 / Adobe Acrobat 9.53 Paper Capture Plug-in