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We tested the widely accepted hypothesis that spotted hyaenas (Crocuta crocuta) are non-selective in their diet. The prey preference of spotted hyaena was studied in the Addo Elephant National Park (AENP), South Africa. Diet (frequency of occurrence of prey items in the diet) was quantified through the analysis of 55 scats, and compared with available prey. A combination of large- and medium-sized mammals (buffalo (Syncerus caffer), red hartebeest (Alcelaphus buselaphus) and common duiker (Sylvicapra grimmia) were the most preferred prey items. The most abundant species, warthog (Phacochoerus africanus) and kudu (Tragelaphus strepsiceros), were ignored and avoided, respectively. These results show that the assumption that hyaena prey on the most abundant available prey species may be overly simplistic. Predation patterns, such as the ones observed in AENP, may have important ramifications for less common species that are selected by hyaena in small enclosed reserves
Hyaenids reached their peak diversity during the Mio−Pliocene, when an array of carnivorous species emerged alongside dwindling civet−like and mongoose−like insectivorous/omnivorous taxa. Significantly, bone−cracking morphological adaptations were poorly developed in these newly−emerged species. This, their general canid−like morphology, and the absence/rarity of canids in Eurasia and Africa at the time, has led researchers to hypothesise that these carnivorous Mio−Pliocene hyaenas were ecological vicars to modern canids. To shed further light on their diets and foraging strategies, we examine and compare the dental microwear textures of Hyaenictitherium namaquensis, Ikelohyaena abronia, Chasmaporthetes australis, and Hyaenictis hendeyi from the South African Mio−Pliocene site of Langebaanweg with those of the extant feliforms Crocuta crocuta, Acinonyx jubatus, and Panthera leo (caniforms are not included because homologous wear facets are not directly comparable between the suborders). Sample sizes for individual fossil species are small, which limits confidence in assessments of variation between the extinct taxa; however, these Mio−Pliocene hyaenas exhibit surface complexity and textural fill volume values that are considerably lower than those exhibited by the living hyaena, Crocuta crocuta. Dental microwear texture analysis thus supports interpretations of craniodental evidence suggesting low bone consumption in carnivorous Mio−Pliocene hyaenas.
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