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Veeckman J,. (1978). Afwijkend sexuell gedrag van een dekhengst. Vlaams Diergeneeskundig Tijdschr, 47, 267–273.
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Veeckman J,. (1978). Preliminary studies on the behavioural detection of oestrus in belgian “warmblood” mares with acoustic and tactile stimuli. Appl Anim Ethol, 4, 109–118.
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Herron, M. A., Martin, J. E., & Joyce, J. R. (1978). Quantitative study of the decussating optic axons in the pony, cow, sheep, and pig. Am. J. Vet .Res., 39(7), 1137–9.
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Murphy, L. B. (1978). The practical problems of recognizing and measuring fear and exploration behaviour in the domestic fowl. Anim. Behav., 26, Part 2, 422–431.
Abstract: In studying behaviour supposedly motivated by fear or by exploration, consideration should be given to the biological functions of these two systems and to the ways in which the experimental environment may affect the performance of ‘natural’ responses. Extreme caution is needed in comparing the effectiveness of different stimuli and the amounts of fear or exploration represented by different responses. In particular, it should never be assumed when making such comparisons that the relative intensities of different stimuli and responses are constant.
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Parker, G. A., & MacNair, M. R. (1978). Models of parent-offspring conflict. I. Monogamy. Anim. Behav., 26, 97–110.
Abstract: Theoretical models for Trivers (1974) concept of parent-offspring conflict are examined for species in which the effects of the conflict are felt by full sibs. A rare conflictor gene will spread if Image , whereÆ’(m) is the fitness gained by a conflictor relative to a non-conflictor offspring (Æ’(m) >1), and m is the amount of parental investment taken by a conflictor relative to m = 1 for a non-conflictor. The range of m alleles which can spread against the parent optimum decreases as the cost to the parent increases until a point is reached where there is no conflict of evolutionary interests. There would be no polymorphism for conflictor: non-conflictor alleles unless special conditions prevail. The conflictor allele which spreads most rapidly as a rare mutant against the parental optimum is not an evolutionarily stable strategy (ESS). The ESS for parent-offspring conflict in monogamous species has m0 = Æ’(m0)/2[dÆ’(m0)/dm0]. The analytical solutions are confirmed throughout by simulations.
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Dickinson, A., & Mackintosh, N. J. (1978). Classical Conditioning in Animals. Annual Review of Psychology, 29(1), 587–612.
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Sorensen, A. B. (1978). Mathematical Models in Sociology. Annual Review of Sociology, 4(1), 345–371.
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Houpt, K. A., Law, K., & Martinisi, V. (1978). Dominance hierarchies in domestic horses. Appl. Animal. Ethol., 4(3), 273–283.
Abstract: Dominance hierarchies were studied in 11 herds of domestic horses and ponies (Equus caballus). A paired feeding test was utilized to establish the dominance--subordination relationship between each pair of animals in a herd. Aggressive actions, threats, bites, kicks and chases were also recorded. In small herds linear hierarchies were formed, but in large herds triangular relationships were observed. Aggression was correlated with dominance rank. Body weight, but not age, appear to affect rank in the equine hierarchy. Juvenile horses were more likely to share feed with each other than were adult horses and were usually subordinate to adult horses. The daughters of a dominant mare were dominant within their own herds.
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Premack D, & Woodruff G. (1978). Does the chimpanzee have a theory of mind? Behav. Brain Sci., 1, 515.
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Stammbach, E. (1978). On Social Differentiation in Groups of Captive Female Hamadryas Baboons. Behaviour, 67(3-4), 322–338.
Abstract: The social differentiation in small groups of captive female hamadryas baboons was examined. Two positions could be distinguished: The highest ranking female, denoted as central individual, monopolized nearly all the presenting, mounting and grooming interactions. The lower ranking females, denoted as peripheral individuals, competed for access to the central female. All dyads of a group were arranged in a rank order according to the amount of sociopositive interaction which they reached within the group. This order of prevalence of dyads was positively correlated with the sum of dominance ranks of the dyad and the mutual attraction as estimated by choice tests. A multiple rank correlation demonstrated that the influence of the sum of ranks and of mutual attraction were nearly independent. If an individual's relationship to the central female had a higher rank of prevalence than that of its rival, it intervened more often and more successfully when the rival tried to interact with the central female. Interventions served to defend rather than to establish relationships. The results are compared with other studies that discuss basic principles governing structuring processes in nonhuman primate groups.
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