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Waring Gh,. (1979). Behavioral adaptation as a factor in management of feral equids.
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Connor, R. C. (1995). Altruism among non-relatives: alternatives to the 'Prisoner's Dilemma'. Trends Ecol Evol, 10(2), 84–86.
Abstract: Triver's model of reciprocal altruism, and its descendants based on the Prisoner's Dilemma model, have dominated thinking about cooperation and altruism between non-relatives. However, there are three alternative models of altruism directed to non-relatives. These models, which are not based on the Prisoner's Dilemma, may explain a variety of phenomena, from allogrooming among impala to helping by non-relatives in cooperatively breeding birds and mammals.
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Matsumura, S., & Kobayashi, T. (1998). A game model for dominance relations among group-living animals. Behav. Ecol. Sociobiol., 42(2), 77–84.
Abstract: Abstract We present here an attempt to understand behaviors of dominant individuals and of subordinate individuals as behavior strategies in an asymmetric “hawk-dove” game. We assume that contestants have perfect information about relative fighting ability and the value of the resource. Any type of asymmetry, both relevant to and irrelevant to the fighting ability, can be considered. It is concluded that evolutionarily stable strategies (ESSs) depend on the resource value (V), the cost of injury (D), and the probability that the individual in one role will win (x). Different ESSs can exist even when values of V, D, and x are the same. The characteristics of dominance relations detected by observers may result from the ESSs that the individuals are adopting. The model explains some characteristics of dominance relations, for example, the consistent outcome of contests, the rare occurrence of escalated fights, and the discrepancy between resource holding potential (RHP) and dominance relations, from the viewpoint of individual selection.
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Kavaliers, M., Colwell, D. D., & Choleris, E. (2005). Kinship, familiarity and social status modulate social learning about “micropredators” (biting flies) in deer mice. Behav. Ecol. Sociobiol., 58(1), 60–71.
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Asa Cs,. (1979). Sociosexual behavior in the domestic pony. In Symposium on the Ecology and Behavior of Wild and Feral Equids (pp. 59–70). Laramie: Univ. of Wyoming.
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Houston, A. I., & McNamara, J. M. (1988). Fighting for food: a dynamic version of the Hawk-Dove game. Evol. Ecol., 2(1), 51–64.
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Ben-Shahar, R. (1995). Habitat classification in relation to movements and densities of ungulates in a semi-arid savanna. Afr. J. Ecol., 33, 50–63.
Abstract: Habitat types were classified in a semi-arid nature reserve in South Africa in order to assess the spatial requirements of resident ungulates, namely zebra, wildebeest and impala. Multivariate analyses showed patterns of soil factors and plant species associations that corresponded with variations of local geological formations and the abundance of plants. The response of ungulates to habitats of different degrees of complexity in terms of soils and plant species associations was examined on the basis of annual occurrence. New habitat types were described through merging or subdividing the existing classification. New habitat categories which corresponded with high occurrences of ungulates provided better indications of the resource requirements for large herbivores. Wildebeest were restricted in their habitat requirements and were characterized by high seasonal densities in bottom lands, particularly during the late wet period. There was a considerable overlap in the preference of habitat types between wildebeest and zebra although zebra were aggregated during longer periods within the dolerite formation. Impala had a consistent annual preference for the granite formation where seepage lines and bottom lands were inhabited seasonally by large herd concentrations.
Résumé
On a classifié les types d'habitat dans une réserve naturelle semiaride d'Afrique du Sud, dans le but d'évaluer les exigences spatiales des ongulés qui y vivent, c'est à dire les zèbres, les gnous et les impalas. Des analyses multivariées ont révélé des schémas pour les facteurs du sol et pour les associations d'espèces végétales qui correspondent aux variations des formations géologiques locales et à l'abon-dance des plantes. On a examiné la réponse des ongulés à des habitats de complexité différente en termes de sols et d'associations d'espéces végétales, d'après leur présence annuelle. On a décrit de nouveaux types d'habitats en fusionnant ou en subdivisant la classification existante. Les nouvelles catégories d'habitats qui correspondaient à des présences abondantes d'ongulés ont fourni de meilleures indications sur les ressources exigées par les grands herbivores. Les gnous se limitaient aux endroits qui répondaient a leurs exigences et se caractérisaient par de hautes densités saisonnières dans les régions basses, spécialement pendant la dernière saison des pluies. Il y avait un recouvrement considérable des types d'habitats préferés par les gnous et les zébres, encore que les zébres se rassemblent plus longtemps dans la formation doléritique. Les impalas marquent une préférence annuelle constante pour la formation granitique où les sources et les terres basses sont occupées de façon saisonnière par des hardes très concentrées.
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McNaughton, S. J., & Georgiadis, N. J. (1986). Ecology of African Grazing and Browsing Mammals. Annual Review of Ecology and Systematics, 17, 39–66.
Abstract: INTRODUCTION Africa is the earth's second largest continent, comprising 20% of its surface. Largely tropical, Africa extends as well into temperate zones to 37 N and 35 S. Eastern and southern Africa display steep elevation gradients due to the prevalence there of volcanic orogeny and rifting (29). Local landscapes are distinguished by substantial geological heterogeneity, dissected land forms, and resultant steep gradients of precipitation and vegetation. The consequent pronounced fragnientation of habitats and sharp juxtaposition of distinct vegetation types, combined with climatic oscillations in geological time, contributed to major adaptive radiations of the mammalian fauna (102, 120). Early zoological expeditions recorded that habitat fragmentation and wide spatial variation of animal densities and diversities were distinctive features of African ecosystems (92, 138, 162, 226). Those early records provided the bases of natural history information on animal distributions, habitat preferences, feeding habits, and general ecology; scientific research followed only much later (201). Modem scientific study of African savanna-grassland mammals began in the 1950s (23, 24, 107, 108, 148, 149, 197,203, 204, 210,230), long after the distributions and densities of the major game animals had been affected by growing human populations, colonial land and hunting policies, and virulent exotic diseases that affected the animals both directly and indirectly (57). The mammalian fauna has been increasingly isolated and fragmented within game reserves of varying size, habitat diversity, and animal species diversity; the ability to sustain it in the absence of active management is increasingly questioned (112, 187). For species with population sizes greater than 100 individuals, game reserve area (A) and faunal ...
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Krama, T. [1], & Krams, I. [2]. (2005). Cost of mobbing call to breeding pied flycatcher, Ficedula hypoleuca. Behav. Ecol., 16, 37–40.
Abstract: Mobbing signals advertise the location of a stalking predator to all prey in an area and recruit them into the inspection aggregation. Such behavior usually causes the predator to move to another area. However, mobbing calls could be eavesdropped by other predators. Because the predation cost of mobbing calls is poorly known, we investigated whether the vocalizations of the mobbing pied flycatcher, Ficedula hypoleuca, a small hole nesting passerine, increase the risk of nest predation. We used mobbing calls of pied flycatchers to examine if they could lure predators such as the marten, Martes martes. This predator usually hunts by night and may locate its mobbing prey while resting nearby during the day. Within each of 56 experimental plots, from the top of one nest-box we played back mobbing sounds of pied flycatchers, whereas blank tapes were played from the top of another nest-box. The trials with mobbing calls were carried out before sunset. We put pieces of recently abandoned nests of pied flycatchers and a quail, Coturnix coturnix, egg into each of the nest-boxes. Nest-boxes with playbacks of mobbing calls were depredated by martens significantly more than were nest-boxes with blank tapes. The results of the present study indicate that repeated conspicuous mobbing calls may carry a significant cost for birds during the breeding season.
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ANGLE M, et al. (1979). Androgenes in feral stallions. Laramie.
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