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Horrocks, J. A., & Hunte, W. (1983). Rank Relations in Vervet Sisters: A Critique of the Role of Reproductive Value. Am. Nat., 122, 417–421.
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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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Nallan, G. B., Pace, G. M., McCoy, D. F., & Zentall, T. R. (1983). The role of elicited responding in the feature-positive effect. Am J Psychol, 96(3), 377–390.
Abstract: Hearst and Jenkins proposed in 1974 that elicited responding accounts for the feature-positive effect. To test this position, pigeons were exposed to a feature-positive or feature-negative discrimination between successively presented displays--one consisted of a red and a green response key and the other consisted of two green response keys. There were four main conditions: 5-5 (5-sec trials, 5-sec intertrial intervals), 5-30, 30-30, and 30-180. Conditions 5-30 and 30-180 should produce the largest amount of elicited responding, and therefore the largest feature-positive effects. A response-independent bird was yoked to each response-dependent bird to allow direct assessment of the amount of elicited responding generated by each condition. Contrary to the predictions by Hearst and Jenkins's theory, response-dependent birds showed large feature-positive effects in each condition. The largest feature-positive effect was obtained in condition 5-5. Response-independent birds produced similar results, but manifested low response rates.
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Wolfe, J. M. (1983). Hidden visual processes. Sci Am, 248(2), 94–103.
Abstract: Isoluminant stimulus is an image whose edges are defined only by a change in color, not by change in brightness. The stimulus here is imperfect: the blue parts and the green parts of the image are only as nearly equal in brightness as they can be on the printed page. Moreover, the change in brightness beyond the edge of the page is apparent, and so is the fact that the reader is holding the magazine at reading distance. When such cues are removed under laboratory conditions, subjects faced with an isoluminant stimulus prove unable to bring its edges into focus. This deficiency contributes to making a familiar face hard to recognize. The experiment indicates that the brain process underlying visual accommodation (the focusing of the eyes) cannot “see” color; it is a hidden process distinct from the processes that lead to perception. The image shows Groucho Marx as he appeared in the motion picture Horse Feathers.
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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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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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Hinde, R. A. (1983). A conceptural framework. In R. A. Hinde (Ed.), Primate Social Relationships (pp. 1–7). Massechusetts: Sinauer, Sunderland.
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Crook, J. H. (1983). On attributing consciousness to animals. Nature, 303(5912), 11–14.
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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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Langlois, B., Minkema, D., & Bruns, E. (1983). Genetic problems in horse breeding. Livestock Production Science, 10(1), 69–81.
Abstract: The purpose of this paper is to give a short survey of the present problems concerning the genetic improvement of horse breeds. The evolution of these populations in Europe, characterized by a deep change from production of draught horses towards that of leisure horses, is described and the influence of the demographical parameters on the selection of these horse populations, is discussed. The generation interval represents an important handicap only surmounted in the case of racing breeds where a high selection intensity can be practised since all animals are subjected to performance testing. In the other cases, the farmer usually does not use modern breeding techniques, but uses crosses instead, which lead more easily to visible results. The available selection criteria are also dealt with. A distinction is made between direct estimates evaluating the abilities of the animals in practice and the indirect estimates measuring a character in correlation to previous ones. For the former estimates, a distinction is made between those resulting from competitions (handicap, records or earnings) and those resulting from direct in-station measurements (saddle, jumping, dressage abilities, draught power). For the indirect estimates, often used especially for the selection of mares, the most important analysis is obviously that of the conformation. However, in the future early selection criteria according to more physiological data should be sought and developed. Estimation of the breeding value according to a given ability is thereafter pointed out. There are two situations: “the panmictic case” concerning sport and draught horses and “the non-panmictic case” corresponding to racing horses, which give rise to some problems. The setting up of breeding plans is discussed. Due to the different economic situations and various objectives of horse production, conclusions are drawn about the role played by geneticists in the present development of this sector.
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