Andersson, M. (1984). Producers and Scroungers.
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Teas, J. (1984). Female Primates: Studies by Women Primatologists.
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Bard J,. (1984). Perch la zebra In:Kos;Revista di Cultura e Storia della. Sci Med, Nat e Humane, 1(6).
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Bökönyi, S. (1984). Horse. In Manson (Ed.), Evolution of domesticated animals (Vol. 18, pp. 162–173). Hoboken, NJ: John Wiley & Sons.
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DUNCAN P et al,. (1984). On lactation and associated behaviour in natural herd of horses. Hans Klingels Equine Reference List, 32, 255–263.
Abstract: Developmental changes in time spent suckling and related mother-foal behaviour are described in an unmanaged herd of Camargue horses. Male foals spent about 40% more time suckling than females during the first 8 weeks. Body weight did not differ between the sexes but time-budgets did: males grazed less and were more active. If pregnant, the typical multiparous mare nursed her foals for 35–40 weeks, males and females alike, and weaned them 15 weeks before the next foaling. Primiparae lactated longer and weaned closer to the next foaling by 5 weeks. The mares played an active role in regulating the time spent suckling in early, and particularly in late lactation.
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KASEDA Y et al,. (1984). Separation and independence of offsprings from the harem groups in Misaki horses. Jap J Zootechn Sci, 55, 852–857.
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Kusunose R, S. H. (1984). The behavioral development of thouroughbred foals and the relationship between dams and foals. Jap J Zootechn Sci, 55, 263–271.
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Mccort Wd,. (1984). Behavior of feral horses and ponies. J Anim Sci, 58, 493–499.
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Kacelnik, A., & Houston, A. I. (1984). Some effects of energy costs on foraging strategies. Anim. Behav., 32(2), 609–614.
Abstract: We consider the effect of including energy costs on the optimal strategy for animals exploiting a depleting food resource. In the context of central place foraging this leads to the problem of what load size should be brought back to the central place. Two strategies are discussed: (i) maximize gross rate of energy delivery and (ii) maximize net rate of energy delivery. The optimal load size (or optimal patch time) for net maximizers is not always larger than for gross maximizers, as has been claimed. Instead, the difference in optimal load size has the same sign as the difference between metabolic rates of travelling and foraging. We point out that the influence of costs has not always been correctly incorporated in experimental tests of the theory.
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Wolff, P. R., & Powell, A. J. (1984). Urine patterns in mice: An analysis of male/female counter-marking. Anim. Behav., 32(4), 1185–1191.
Abstract: Counter-marking in mice, Mus musculus was investigated by analysing urine deposition on filter paper marked asymmetrically with urine of the opposite sex. Intact males deposited large numbers of urine spots with a marked angular bias towards previously marked quadrants. More spots were deposited on proestrous and ovariectomized donor urine patterns, their distribution being more centrifugal on oestrous urine and more centripetal in quadrants containing a large female urine spot in a central position. In contrast, castrated male mice deposited very few spots with no angular bias. Female urine patterns showed angular bias in response to intact, but not castrated male donor urine, a larger number of spots being produced by oestrous females. Thus the pattern of deposition offers scope for two-way communication of information about reproductive potential.
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