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Penzhorn Bl,. (1988). Equus zebra. Mammalian Species, 314, 1–7.
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Hamilton, C. R., & Vermeire, B. A. (1988). Complementary hemispheric specialization in monkeys. Science, 242(4886), 1691–1694.
Abstract: Twenty-five split-brain monkeys were taught to discriminate two types of visual stimuli that engage lateralized cerebral processing in human subjects. Differential lateralization for the two kinds of discriminations was found; the left hemisphere was better at distinguishing between tilted lines and the right hemisphere was better at discriminating faces. These results indicate that lateralization of cognitive processing appeared in primates independently of language or handedness. In addition, cerebral lateralization in monkeys may provide an appropriate model for studying the biological basis of hemispheric specialization.
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Bednarz, J. C. (1988). Cooperative Hunting Harris' Hawks (Parabuteo unicinctus). Science, 239(4847), 1525–1527.
Abstract: Coordinated hunting by several individuals directed toward the capture and sharing of one Large prey animal has been documented convincingly only for a few mammalian carnivores. In New Mexico, Harris' hawks formed hunting parties of two to six individuals in the nonbreeding season. This behavior improved capture success and the average energy available per individual enabled hawks to dispatch prey larger than themselves. These patterns suggest that cooperation is important to understanding the evolution of complex social behavior in higher vertebrates and, specifically, that benefits derived from team hunting a key factor in the social living of Harris' hawks.
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Schilder, M. B. H. (1988). Dominance relationships between adult Plains zebra stallions in semi – captivity. Behaviour, 104(3-4), 300–319.
Abstract: The relationships between 4-5 adult zebra stallions, living in a safari park, were investigated over a period of 5 years. Asymmetries in the distributions of a number of behaviours could be explained by adopting dominance as an intervening variable. Dominance in stallions was of a bipolar nature with on the one hand behaviours representing subordinance and defence, and on the other hand behaviours reinforcing and confirming dominance. Expression of formal dominance seems to play a minor role. The dyadic relationships of stallions differed as to the number of behaviours reflecting dominance relationships. Although often linear rank-orders could be constructed, these rank-orders were not necessarily identical. This means that the concept of dominance is of only limited value for describing relationships between zebra stallions.
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Rogers, A. R. (1988). Does Biology Constrain Culture? Am Anthropol, 90(4), 819–831.
Abstract: Most social scientists would agree that the capacity for human culture was probably fashioned by natural selection, but they disagree about the implications of this supposition. Some believe that natural selection imposes important constraints on the ways in which culture can vary, while others believe that any such constraints must be negligible. This article employs a “thought experiment” to demonstrate that neither of these positions can be justified by appeal to general properties of culture or of evolution. Natural selection can produce mechanisms of cultural transmission that are neither adaptive nor consistent with the predictions of acultural evolutionary models (those ignoring cultural evolution). On the other hand, natural selection can also produce mechanisms of cultural transmission that are highly consistent with acultural models. Thus, neither side of the sociobiology debate is justified in dismissing the arguments of the other. Natural selection may impose significant constraints on some human behaviors, but negligible constraints on others. Models of simultaneous genetic/cultural evolution will be useful in identifying domains in which acultural evolutionary models are, and are not, likely to be useful.
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Thackeray, J. F. (1988). Zebras from wonderwerk cave, northern Cape province, South Africa: attempts to distinguish Equus burchelli and E. quagga. Suid- Afrikaanse Tydsskrif vir Wetenskap, 84, 99–101.
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Westlin-van Aarde, L. M., van Aarde, R. J., & Skinner, J. D. (1988). Reproduction in female Hartmann's zebra. J Reprod Fert, 84, 505–511.
Abstract: Ovaries, fetuses and plasma were collected from zebra mares shot in the Etosha National Park in Namibia between 15 and 25 August 1983. Ovarian weight was affected by reproductive status and most of the non-pregnant mares were anoestrous. The number of follicles varied between individuals and only pro-oestrous/oestrous mares had follicles larger than 20 mm in diameter. The largest follicle in pregnant mares was only 9 mm in diameter. Corpora lutea and corpora albicantia were found in non-pregnant as well as pregnant mares: 4 pregnant mares had only corpora albicantia. The presence of secondary corpora lutea could not be confirmed in any of the pregnant mares. Implantation was estimated to occur at around 73 days of gestation, and most mares (84%) had conceived between November and April. Peripheral concentrations of plasma progesterone during pregnancy varied from 0·5 to 2·4 ng/ml.
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Penzhorn, B. L., & van der Merwe, N. J. (1988). Testis size and onset of spermatogenesis in Cape mountain zebras (Equus zebra zebra). J Reprod Fert, 83, 371–375.
Abstract: Testis mass of adult Cape mountain zebra stallions (mean 70·0 g) was appreciably less than that of other zebra species and domestic horses. The histological appearance of the testes of 11-, 24- and 29-month-old colts was typically prepubertal. Spermatogenic activity of a 4-year-old stallion obtained at the end of summer was at a very low level, while a 4·5-year-old stallion obtained 6 weeks after the winter solstice showed a marked increase in spermatogenesis compared with the 4-year-old. Stallions 6·5-19 years of age collected in different seasons all showed active spermatogenesis.
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Mackintosh, N. J. (1988). Approaches to the study of animal intelligence. British Journal of Psychology, 79, 509–525.
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Black, J. M. (1988). Preflight Signalling in Swans: A Mechanism for Group Cohesion and Flock Formation. Ethology, 79(2), 143–157.
Abstract: Abstract The preflight behaviour of whooper swans Cygnus cygnus and Bewick's swans Cygnus columbianus bewickii was examined to determine the adaptive significance of the ritual. Analysis of the preflight sequence revealed that the rate of signalling became significantly faster as the time of takeoff approached. This provides the first quantitative evidence that a threshold of excitability is responsible for triggering synchronised flight in social units. Two ultimate and two proximate factors that affect this threshold were uncovered. They are: 1) Maintaining proximity to partners—flight was delayed by birds with non-attentive mates and signalling lasted on average four times longer than those whose mates showed more interest. 2) Maintaining flock cohesiveness—birds which performed signals for longer periods while swimming among uninterested birds were successful in attracting followers 61% of the time. 3) The bird's feeding performance related to dominance status—less successful feeders (potentially hungry birds), flew after little time and few signals. 4) The type of feeding opportunity at the eventual destination—birds which flew to provided feeds (nutritious barley) spent less time performing preflight signals than when they flew to forage on grass fields.
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