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Kaseda Y,. (1983). Seasonal changes in the home range and the size of harem groups of Misaki horses. Jpn J Zootech Sci, 54, 254–262.
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Kaseda Y,. (1983). Seasonal changes in time spent grazing and resting of Misaki horses. Jpn J Zootechn Sci, 54, 464–469.
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Reichholf J,. (1983). Warum sind Zebras gestreift? Das Tier, 3, 10–13.
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Waring, G. H. (Ed.). (1983). Horse Behavior: The Behavioral Traits and Adaptations of Domestic and Wild Horses, Including Ponies. Park Ridge: Noyes Publications.
Abstract: ReviewsSynopsisThe second edition of this informative book remains the most comprehensive and current overview of the behavioral traits and adaptations of horses. The book integrates findings from hundreds of international researchers to provide the reader with a factual synthesis of the behaviour of domestic and feral horses. Building on the strengths of the first edition, the author has thoroughly updated coverage of horse ancestry, development, perception, learning, play, social behavioral manipulation, maintenance activities, and sexual behaviour. Throughout these and other chapters, more emphasis has been given to animal husbandry and management. Additionally, the second edition includes an all-new section on ecological influences on activity patterns, habitat utilization, social behaviour and reproduction. An expanded section on applied ethnology provides behavioral considerations or management and insight regarding the behavioral indicators of horse health and well being. This is followed with an updated appendix listing behavioral symptoms and possible causes. The text contains numerous tables and nearly 100 illustrations and photos. Interesting Facts: Rich with international data, incorporated into text, tables, and figures Two new chapters on ecological influences dealing with interactions between environment feeding, ranging, shelter seeking, reproductive and social behavior, among other topics New chapter on behavioral considerations in horse management, plus updated material on health and well being, surveys atypical symptoms ranging from posture to social behaviour Update appendix provides an extensive listing of behavioral symptoms, with identifications of possible associated problems.
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Berger, J. (1983). Induced abortion and social factors in wild horses. Nature, 303(5912), 59–61.
Abstract: Much evidence now suggests that the postnatal killing of young in primates and carnivores, and induced abortions in some rodents, are evolved traits exerting strong selective pressures on adult male and female behaviour. Among ungulates it is perplexing that either no species have developed convergent tactics or that these behaviours are not reported, especially as ungulates have social systems similar to those of members of the above groups. Only in captive horses (Equus caballus) has infant killing been reported. It has been estimated that 40,000 wild horses live in remote areas of the Great Basin Desert of North America (US Department of Interior (Bureau of Land Management), unpublished report), where they occur in harems (females and young) defended by males. Here I present evidence that, rather than killing infants directly, invading males induce abortions in females unprotected by their resident stallions and these females are then inseminated by the new males.
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Moss, C. J., & Poole, J. H. (1983). Relationships and social structure in African elephants. In R. A. Hinde (Ed.), Primate social relationships: an integrated approach.. Blackwell Science Ltd.
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Markworth, P. (1983). Sportmedizin: Physiologische Grundlagen. Reinbek: Rowohlt.
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Heffner, H. E., & Heffner, R. S. (1983). The hearing ability of horses. Equine Pract, 5, 27–32.
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Zentall, S. S., & Zentall, T. R. (1983). Optimal stimulation: a model of disordered activity and performance in normal and deviant children. Psychol Bull, 94(3), 446–471.
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Hogan, D. E., Zentall, T. R., & Pace, G. (1983). Control of pigeons' matching-to-sample performance by differential sample response requirements. Am J Psychol, 96(1), 37–49.
Abstract: Pigeons were trained on a matching-to-sample task in which sample hue and required sample-specific observing behavior provided redundant, relevant cues for correct choices. On trials that involved red and yellow hues as comparison stimuli, a fixed-ratio 16 schedule (FR 16) was required to illuminate the comparisons when the sample was red, and a differential-reinforcement-of-low-rates 3-sec schedule (DRL 3-sec) was required when the sample was yellow. On trials involving blue and green hues as comparison stimuli, an FR 16 schedule was required when the sample was blue and a DRL 3-sec schedule was required when the sample was green. For some pigeons, a 0-sec delay intervened between sample offset and comparison onset, whereas other pigeons experienced a random mixture of 0-sec and 2-sec delay trials. Test trial performance at 0-sec delay indicated that sample-specific behavior controlled choice performance considerably more than sample hue did. Test performance was independent of whether original training involved all 0-sec delay trials or a mixture of 0-sec and 2-sec delays. Sample-specific observing response requirements appear to facilitate pigeons' matching-to-sample performance by strengthening associations between the observing response and correct choice.
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