In ungulates, rank order is determined by differences in weight, body size, weapon size and age. In the Caprini tribe (Bovidae: Caprinae), adult male Himalayan tahr are unique to show different coat colours, but no sexual dimorphism in weapons. A highly significant correlation between hair colour and rank order was found during the rut: males with a lighter coloured ruff dominated over darker ruffed ones, in both aggressive interactions and access to oestrus females. We studied colour-based dominance in relation to weight, age and testosterone levels, which establish the social rank in most ungulates. No differences in weight and testosterone concentrations were found between adult male colour classes, but males with paler ruffs were significantly younger than darker adult males. The distribution of physical traumas from fights confirmed that younger, lighter-coloured males had a higher rank than older, darker males, a pattern which is unusual amongst ungulates. Coat colour seems to work as a signal of rank in male-male aggressive interactions and it changes according to age, whereas the relevant physiological determinants deserve further research. Intrasexual male competition has not changed weapon size or shape in the Himalayan tahr, but ruff colours are apparently used to signal rank and dominance. Colour patterns of adult males may then be homologous to ritualised weapons, apparently being a unique feature of male tahr amongst mammals.

In ungulates, rank order is determined by differences in weight, body size, weapon size and age. In the Caprini tribe (Bovidae: Caprinae), adult male Himalayan tahr are unique to show different coat colours, but no sexual dimorphism in weapons. A highly significant correlation between hair colour and rank order was found during the rut: males with a lighter coloured ruff dominated over darker ruffed ones, in both aggressive interactions and access to oestrus females. We studied colour-based dominance in relation to weight, age and testosterone levels, which establish the social rank in most ungulates. No differences in weight and testosterone concentrations were found between adult male colour classes, but males with paler ruffs were significantly younger than darker adult males. The distribution of physical traumas from fights confirmed that younger, lighter-coloured males had a higher rank than older, darker males, a pattern which is unusual amongst ungulates. Coat colour seems to work as a signal of rank in male-male aggressive interactions and it changes according to age, whereas the relevant physiological determinants deserve further research. Intrasexual male competition has not changed weapon size or shape in the Himalayan tahr, but ruff colours are apparently used to signal rank and dominance. Colour patterns of adult males may then be homologous to ritualised weapons, apparently being a unique feature of male tahr amongst mammals.

Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium–large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a ‘near-threatened’ caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8–0.9) was high. The decrease of this ratio to 0.1–0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.

Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium–large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a ‘near-threatened’ caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8–0.9) was high. The decrease of this ratio to 0.1–0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.