The response of spotted hyaenas to long‐term changes in prey populations: functional response and interspecific kleptoparasitism

Abstract

Summary1. Over the last three decades the main prey species (wildebeest Connochaetes taurinus , zebra Equus burchelli , Thomson's gazelle Gazella thomsoni , and Grant's gazelle Gazella granti ) of spotted hyaenas Crocuta crocuta in the Ngorongoro Crater, Tanzania, substantially declined in numbers, whereas buffalo Syncerus caffer numbers increased strongly. This provided a 'natural experiment' to investigate how a generalist predator such as the spotted hyaena responds to long-term changes in prey populations. Here we compare data on the feeding ecology of Crater hyaenas from the late 1990s ( period II) with equivalent data from the late 1960s (period I). 2. Hyaenas showed strong hunting preferences for wildebeest calves and gazelle fawns during both periods I and II. Adult buffaloes, prey difficult to hunt for hyaenas, were rarely hunted in either period despite a large increase in buffalo numbers from period I to II. 3. Hyaenas exhibited a functional response to the changes in prey populations by killing more buffalo calves and adult wildebeest during period II, relatively easy prey categories for hyaenas to hunt. 4. The proportion of carcasses scavenged and acquired by kleptoparasitizing other predators increased from period I to II. This was facilitated by an increase in the relative number of lion kills available to hyaenas during the same period. 5. Hyaenas defended a similar proportion of their kills against kleptoparasitic attempts by lions during both periods. Since the ratio of kills hyaenas kleptoparasitized from lions in relation to kills lost to lions increased from period I to period II, hyaenas obtained more food resources from lions during period II than I. 6. The success of hyaenas kleptoparasitizing lions was influenced by the presence of male lions and the ability of hyaenas to recruit sufficient clan members to appropriate carcasses from lions. 7. This study is the first to demonstrate both a functional response of a predator to changes in the size of prey populations and an associated change in foraging behaviour of the predator.

Late Pleistocene mammalian assemblages of Southeast Asia: New dating, mortality profiles and evolution of the predator–prey relationships in an environmental context

“…Unlike the tiger (~150 kg), the spotted hyena (60-80kg), generally nocturnal or crepuscular, hunts alone, in small groups or sometimes in large packs up to 25 individuals (Kruuk, 1972;Boitani and Bartoli, 1984;Turner and Anton, 1997;Nowak, 1999;Cooper et al, 1999;Höner et al, 2002;Francis, 2008). At Nam Lot, it is obvious that only the formation of large packs compensated for their small body size, when hunting large ungulates.…”

Prey selection and dietary response by wolves in a high-density multi-species ungulate community

“…Secondly, age-related selection patterns of all prey species were analysed according to each species' classification into two age classes: <1-year-old individuals and adults (Höner et al 2002). This analysis was performed using only data from 1993 to 1996 for which the annual sample size was >100 scats.…”

Comprehensive phylogeny of apid bees reveals the evolutionary origins and antiquity of cleptoparasitism

“…Cleptoparasitism (or kleptoparasitism), which involves the stealing of food or nesting material by one animal from another, is a widespread phenomenon found in many animal groups, including birds (6), bees (7), wasps (8), spiders (9), fish (10), and mammals (11). In bees, cleptoparasitic species do not build or provision their own nests; instead, they enter the nests of other bees and lay their eggs in either closed or open, partially provisioned brood cells (12).…”