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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Berger, J., & Cunningham, C. (1988). Size-Related Effects on Search Times in North American Grassland Female Ungulates. Ecology, 69(1), 177–183.
Abstract: Feeding and searching (= vigilance) rates arise as a result of many interrelated factors including trophic level, diet, reproductive condition, sex, habitat, body mass, and potential predation pressure. Because of unique ecological conditions in which the confounding influences of all but two of these variables could be minimized, we examined the hypothesis that body mass alone accounts for interspecific differences in search times, and tested it with females of four sympatric native North American ungulates (Bison bison, Antilocapra americana, Ovis canadensis, and Odocoileus hemionus). When the effects of group size were controlled, smaller bodied species were more vigilant (per unit body mass) than larger ones. However, search times (ST) also scaled to body mass, and between 81 and 97% of the ST variance was explained by either exponential or power functions. To remove the potential bias that predators exert different influences on species of varying size, search times of bison in areas with and without their major predator, wolves (Canis lupus), were contrasted; search times did not differ between sites. Our results highlight the importance of designing field research that controls for confounding variables prior to attempting to scale behavioral processes to ecological events. See full-text article at JSTOR
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Berger, J.,. (1988). Social systems, resources, and phylogenetic inertia: an experimental test and its limitations. In C. N. Slobochikoff (Ed.), Ecology of Social Behavior (pp. 157–186). San Diego: Academic Press.
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Edwards, P. J., & Hollis, S. (1982). The Distribution of Excreta on New Forest Grassland Used by Cattle, Ponies and Deer. J Appl Ecol, 19(3), 953–964.
Abstract: (1) The distribution of excreta on areas of reseeded grassland in the New Forest used by free-ranging cattle, ponies and fallow deer was shown to be non-random. Distinct latrine areas were recognized where the faeces of all three herbivore species were concentrated, and where the majority of urinations occurred. The mosaic of latrine and non-latrine areas can be detected in aerial photographs in which non-latrine areas appear as light-grey patches set in a matrix of the dark grey latrine areas. During the 3 years of the study the position of the mosaic proved to be relatively stable. (2) The latrine areas were characterized by an uneven sward about 50 mm tall with abundant thistles (Cirsium spp.) and ragwort (Senecio jacobaea). Non-latrine areas had an even and very closely cropped sward between 10 and 20 mm tall. Soil chemical analysis of the two kinds of area revealed significantly higher levels of exchangeable potassium in latrine areas, and on one site significantly higher levels of magnesium and organic matter. No significant differences were detected in soil reaction, nor in phosphorus or calcium levels. (3) Observations of grazing animals revealed a tendency, at all times of year, for ponies to avoid grazing in latrine areas. In winter and spring this tendency was very slight, but from midsummer until late autumn a substantial majority of grazing ponies were to be found in non-latrine areas. In contrast, only 2% of the cattle observations made over a period of 20 months were of animals grazing in non-latrine areas. (4) The standing crop of dung and the rate of dung production on the two kinds of area were monitored for 12 months on one lawn. The amount of pony dung produced on non-latrine areas was only 16.5% of that in latrine areas, while for cattle the corresponding value was 28.7%. It is argued that the observed pattern has been created by selective grazing and eliminatory behaviour of the ponies, and that the excreta of cattle and deer are largely confined to pony latrine areas because these animals are unable to graze the very short herbage of non-latrine areas.
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Dellert, B., & Ganslosser, U. (1997). Experimental alterations of food distribution in two species of captive equids (Equus burchelli and E. hemionus kulan). Ethol Ecol Evol, 9(1), 1–17.
Abstract: n one group each of Plains zebra (six mares, one foal, one subadult) and Asiatic wild asses (seven mares, two foals) at Nuremberg Zoo, food distribution was experimentally changed from clumped (all food in one standard hay rack) to dispersed (one heap per animal). Both groups were characterized by different social structures, which basically remained during the experiment. Plains zebras had an individually structured system of social relationships in a dominance order, wild asses a more egalitarian system without clear-cut rank differences and low frequencies of agonistic interactions. Access to food accordingly was individually (but consistently) different for zebra mares, almost equal for wild ass mares. During the dispersed feeding situation frequencies of agonistic interactions in both species decreased (however non-significantly), individual distances increased but mares also frequently ''visited'' each others' heaps. Feeding time increased for all wild ass mares. Some individuals (in both groups) behaved ''against the trend'' in agonistic behaviour. The results are discussed with regard to food distribution for ungulates in general, and equid social systems.
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Podos, J. (1964). Early perspectives on the evolution of behavior: Charles Otis Whitman and Oskar Heinroth. Ethol Ecol Evol, 6(4), 467–480.
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Garott, R. A. (1991). Sex Ratios and Differential Survival of Feral Hors. J Anim Ecol, 60(3), 929–936.
Abstract: (1) Sex and age data were collected on 60 111 feral horses (Equus caballus L.) removed from eighty-nine areas in Nevada, Wyoming, and Oregon between 1976 and 1987. (2) Sex ratios of young seldom differed from parity; however, sex ratios of adults were commonly skewed toward females. No evidence of differential capture probability between adult males and females could be detected; therefore, skewed adult sex ratios were attributed to differential survival. (3) Age-specific trends in sex ratios indicated that the proportion of males steadily decreased from near parity in foals, to lows of 0.61-0.77 in the 4-5-year age-classes. The trend then reversed with males becoming predominant (1.08-1.36) in the > 10 years age-class. (4) Population simulations suggest that survival diffentials of 0.05-0.07, favouring females to 4 years of age, and 0.02-0.04 favouring males in older age-classes were required to mimic observed age-specific sex ratio changes. To obtain the high proportion of males in the > 10-years age-class, onset of senescence also had to be earlier for females. (5) Causes for differential survival in the immature age-classes are uncertain, but may relate to behavioural or metabolic differences between the sexes. Differential survival between adult males and females is attributed to differences in the energetic costs of reproduction and disparity in their reproductive life spans.
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Kahurananga, J., & Silkiluwasha, F. (1997). The migration of zebra and wildebeest between Tarangire National Park and Simanjiro Plains, northern Tanzania, in 1972 and recent trends. Afr J Ecol, 35(3), 179–185.
Abstract: In 1972, four aerial censuses were carried out to assess the annual migration of zebra and wildebeest between Tarangire National Park and Simanjiro Plains. About 6000 zebra and 10,000 wildebeest were in the Plains in the middle of the rainy season, in April. During the dry season in August the animals were concentrated in the Park. The migration from the Park to the Plains started at beginning of the rains, in November/December. Recent censuses by Tanzania Wildlife Conservation Monitoring (TWCM, 1991, 1995) indicate that an estimated 23,000 zebra and 11,000 wildebeest migrate into the Park from Simanjiro and other wet season areas. Encroaching cultivation is a threat to the migration corridors and sustainability of the ecosystem . Providing benefits from wildlife to communities around the park would safeguard the future of the wildlife.
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Eisenberg, J. F., & Kleiman, D. G. (1972). Olfactory Communication in Mammals. Annu Rev Ecol Systemat, 3(1), 1–32.
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Kirkpatrick, J. F., & Turner, J. W. (1991). Changes in herd stallions among feral horse bands and the absence of forced copulation and induced abortion. Behav. Ecol. Sociobiol., 29(3), 217–219.
Abstract: Forced copulation and induced abortion were investigated in a herd of feral horses inhabiting a coastal barrier island. Eight mares were diagnosed pregnant in August and October 1989 by means of urinary and fecal steroid metabolites, prior to documented changes in herd stallions. These mares were observed for harassment and forced copulation by the new stallions and for the presence of foals during the spring and summer of 1990. No incidents of harassment or attempts at forced copulation were witnessed and seven of the eight mares produced foals in 1990. These data indicate that forced copulation and induced abortion are not common events among all feral horse herds and suggest reinvestigation of this hypothesized phenomenon.
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