Many studies have concluded that territoriality is absent in male bushbuck Tragelaphus scriptus but a minority has suggested that some exclusive mechanisms act between adult males. This study provides indirect evidence for the existence of territorial structures between adult male bushbuck by comparing home-range overlap between adult and sub-adult males. The spatial organization of individuals in relation to each other was established by using numerical classification. Location fixes of 52 males, each individual distinguished by a characteristic coat pattern, were taken over a period of 3 years. Home ranges were estimated using the fixed kernel density estimator. Two indices (coefficient of overlap, index of overlap) were applied to compare home-range overlap between the different male age classes. There was a strong home-range overlap up to the 30% home-range core between sub-adult as well as between adult and sub-adult males, while adult male home ranges overlapped up to the 50% home-range core only. It could be shown that home ranges of adult males overlapped significantly less than those of sub-adult males and those between sub-adult and adult males indicating an exclusive use of central core areas (home sites). Sub-adult males form bachelor pools without being permanently associated. With increasing age, sub-adult males challenge territory holders and replace them in order to take over their exclusive areas. These maturing sub-adult males (young adults), often focused on a particular territory holder denoting the young adults as prospects or candidates.

Many species of gazelles (Gazella spp.) are nowadays threatened by hunting, poaching, habitat loss and habitat deterioration. Conservation efforts for this group not only face the problem of maintaining remnant populations, but often natural populations have been extirpated from the wild. In some cases, though, captive breeding programs exist that might provide a valuable source for future reintroductions. A major problem in this context is that phylogeographic relationships among different (potentially locally adapted) populations, and even basic phylogenetic relationships between species, are poorly understood, thus hampering the assignment of management units, breeding groups or stocks for reintroduction projects. Our present study focused on Dorcas gazelles (G. dorcas and G. saudiya) from the species' entire distribution range, with samples originating from western Saharan Africa into Saudi Arabia. In stark contrast to previous studies reporting on pronounced genetic structure in taxa such as Mountain gazelles (G. gazella), we detected low genetic diversity and no evidence for major phylogenetic lineages when analyzing two mitochondrial genetic markers. Using a coalescent approach we infer a steep population decline that started approximately 25,000 years before present and is still ongoing, which coincides with human activities in Saharan Africa. Our phylogenetic analyses, statistical parsimony network analysis and inferred colonization patterns shed doubt on the validity of various described subspecies of G. dorcas.

Intersexual and seasonal variation in foraging behaviour of impala (Aepyceros melampus), was studied in the Lake Mburo National Park, Uganda.There was a moderate seasonal di¡erence in foraging e⁄ciency (as measured by 'acceptable food abundance'), with a minimum in dry season and a maximum in Rainy season. The variation between sexes was more distinct with a pronounced minimum in time spent browsing of males in early wet season. By distinguishing between feeding time spent grazing and feeding time spent browsing the seasonal variation was con¢rmed. The proportion of foraging time spent feeding (expressed as 'food ingestion rate') showed an inverse pattern with a maximum in the late dry season (75.5%), decreasing values throughout the Rainy season and a minimum in early dry season (57.8%). Di¡erences between sexes were explained in terms of reproductive demands and seasonal balance in terms of moderate climate throughout the year. Impala foraging patterns in the bimodal tropics (two Rainy seasons) is discussed and compared with unimodal tropics. The ¢ndings are matched against current ideas on optimal foraging.