Poenskop Cymatoceps nasutus (Pisces: Sparidae), an endemic South African sparid, is an important angling species being predominantly targeted by the recreational shore and skiboat sector. This species is slow-growing, long-lived, late-maturing and sex-changing, making poenskop acutely sensitive to over-exploitation. Despite interventions, such as the imposition of size and bag limits (currently 50 cm TL and one per licensed fisher per day) by authorities, catch-per-unit-effort trends reflect a severe and consistent stock decline over the last two decades. Poenskop has been identified as a priority species for research and conservation. Although the biology and population dynamics of this species have been well-documented, little is known about the movement behaviour of poenskop. Furthermore, there is a complete lack of information on its genetic stock structure. This thesis aimed to address the current knowledge gaps concerning movement behaviour and genetic stock structure of poenskop, making use of a range of methods and drawing on available information, including available fishery records as well as published and unpublished survey and research data, and data from long-term monitoring programmes. Analysis of available catch data (published and unpublished) revealed a decline in the number of poenskop caught as well as size of fish taken over the last two decades, ultimately reflecting the collapse of the stock (estimated to be at 20% of their pristine level). Improved catch-per-unit-effort data from the Tsitsikamma National Park Marine Protected Area (MPA), and larger poenskop being caught in the no-take areas than adjacent exploited areas of the Pondoland MPA confirmed that MPAs can be effective for the protection and management of poenskop. The current MPA network in South Africa is already wellestablished, and encompasses considerable reef areas, being preferable for poenskop habitation. Conventional dart tagging and recapture information from three ongoing, long-term fishtagging projects, conducted throughout the poenskop’s distribution, indicated high levels of residency at all life-history stages. Coastal region, seasonality and time at recapture did not appear to have a significant effect on the level of movement or distance moved. However, on examining the relationship among coastal movements and fish size and ages, larger and older fish (adults) moved greater distances, with juveniles and sub-adults showing high degrees of residency. An estimation of home-range size indicated smaller poenskop to hold smaller home-ranges, while larger poenskop hold larger home-ranges. Large easterly displacements of a number of adult poenskop is in accordance with previous findings that this species may undertake a unidirectional migration up the coastline of South Africa where they possibly settle in Transkei waters for the remainder of their lives. This high level of residency makes poenskop vulnerable to localised depletion, although they can be effectively protected by suitable MPAs. Despite considerable tagging effort along the South African coastline (2 704 poenskop tagged with 189 recaptures, between 1984 and 2010), there remains limited information on the connectivity of different regions along the South African coastline. This was addressed using mitochondrial DNA sequencing. The mitochondrial DNA control region was used due to its high substitution rate, haploid nature, maternal inheritance and absence of recombination. The mtDNA sequencing showed no evidence of major geographic barriers to gene flow in this species. Samples collected throughout the core distribution of poenskop showed high genetic diversity (h = 0.88, π = 0.01), low genetic differentiation among regions, no spatial structure (ɸST = 0.012, p = 0.208) and no evidence of isolation by distance. The collapsed stock status of poenskop as well as the fact that it is being actively targeted by recreational and commercial fishers suggests that this species requires improved management, with consideration given to its life-history style, residency and poor conservation status. Management recommendations for poenskop, combined with increasing South Africa’s existing MPA network, include the possibility of setting up a closed season (during known spawning periods) as well as the decommercialisation of this species. The techniques used and developed in this study can also be adopted for other overexploited linefish species.

M.Sc. / Hydrocynus vittatus, commonly known as the tigerfish, plays an important role in riverine ecology. It is a top predator which roams the open waters of most larger river systems in southern Africa. Their presence in a freshwater ecosystem has a dramatic impact on the fish community structure. It is known that dams and weirs have a negative effect on the migration of the tigerfish. It is also evident that tigerfish do not occur in certain areas in some of the rivers where they have been present historically. The Olifants and Letaba Rivers in the Kruger National Park (KNP) are two of a few rivers within South Africa where tigerfish do occur. The KNP represents the edge of the most southern distribution of tigerfish in southern Africa. It was therefore expected that the tigerfish do not function optimal in the Olifants and Letaba Rivers as they are subjected to waters with high concentrations of silt and low flow which influences migration and successful breeding. Breeding migrations does however take place during the summer months after which the tigerfish returns to the Massingire Dam in Mozambique to avoid the colder winter temperatures in the rivers. Gonad development coincide with the yearly summer rainfall patterns. A deviation of the expected 1:1 male:female sex ratio to favour the males was experienced in both rivers, which may be the result of over population. Females were found to grow to a larger size than the males and were extremely fecund. Although H. vittatus is believed to be mainly piscivorous, other food items such as invertebrates, played an important role in the diet of small and large tigerfish in both the Olifants and Letaba Rivers. Invertebrates were mostly preyed upon which implies that optimal feeding conditions for the tigerfish does not prevail in these systems and that they have to adapt to satisfy their feeding requirements. Tigerfish is more abundant in the Olifants than in the Letaba River. The overall growth performance or phi prime (4)) values for H. vittatus in the Olifants River was determined and compares well to the overall growth performance of tigerfish in the Okavango River and Lake Kariba. However the maximum length calculated for tigerfish in the Olifants River (Lco = 52.40 cm ) is smaller than the Lco values (56.06 cm) for the Okavango River. The mortality rate of tigerfish in the Olifants River exceeds those in the Letaba River which means that the life expectancy is longer in the Letaba as opposed to the Olifants River. Successful artificial spawning revealed some of the secrets of the reproduction strategy of this species. Tigerfish has semi pelagic eggs, are very small (0.65 mm), negatively buoyant and slightly adhesive for bentic and epibiotic incubation, and it is expected that tigerfish would spawn in open water, on a sandy substrate in the vicinity of aquatic vegetation. First hatching took place at 22h 30 min after fertilization. Vertical movement of the larvae lasts for two days, which allows for downstream movement and dispersement of the larvae. It was found that tigerfish replace their teeth on a regular basis as they grow larger. Transition from conical to functional dentition takes place 45 days after hatching. Replacement of sets of teeth occurs during all phases of its lifespan. It is a quick proses of three to six days during which all teeth are replaced in both the upper and lower jaws.