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Dvoinos, G. M., Kharchenko, V. A., & Zviagnitsova, N. S. (1992). The characteristics of the helminth community in the Turkmen kulan (Equus hemionus). Parazitologiia, 26(3), 246–251.
Abstract: The helminth fauna of 24 kulans from Askaniya-Nova and Badkhyz was studied. 42 species of helminths were found, 34 of which belong to strongylids. The helminth species composition of kulan is similar to that of other species of horses. This is a result of an intensive parasite exchange in the historical past when numerous populations of different Equidae species made long seasonal migrations over steppe inter-river lands of Asia and grazed for some time on common pastures.
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Smith-Funk, E. D., & Crowell-Davis, S. L. (1992). Maternal behavior of draft mares (Equus caballus) with mule foals (Equus asinus x Equus caballus). Appl. Anim. Behav. Sci., 33(2-3), 93–119.
Abstract: Draft mares and their mule foals were observed from the day of birth to Week 17 of each foal's life. The rate of nursing was recorded and the duration of nursing activity to the nearest second. The rate at which foals engaged in nursing activity varied at each age. The duration of nursing bouts varied slightly as the foals matured. Aggression was recorded during both nursing and non-nursing activity for both the mares and foals. Maternal aggression was highest during nursing activity, especially during the pre-nurse nuzzling period. Maternal aggression increased as the foals matured. Mother-directed foal aggression was primarily in response to maternal aggression. Spatial relationships between each focal dyad were recorded when the foals were upright, not nursing and when they were recumbent. Spatial relationships differed based on the foal's state. The activity in which the mare engaged while her foal was recumbent was recorded. The movements of the mares were also recorded during foal recumbency. Mares approached or maintained their distance from their recumbent foal more than they left their recumbent foal in all weeks of the study, except Week 2.
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Pruett-Jones, S. (1992). Independent Versus Nonindependent Mate Choice: Do Females Copy Each Other? Am Nat, 140(6), 1000–1009.
Abstract: There is increasing evidence from both observational and experimental studies that females may copy each other's mating decisions. Female copying can be defined as a type of nonindependent choice in which the probability that a female chooses a given male increases if other females have chosen that male and decreases if they have not. The important characteristic of copying behavior that separates it from other similar processes is that the change in the probability of choice is strictly because of the actions of other females and not the consequences of those actions (e.g., a male's behavior changing as a result of successful matings). A gametheory model suggests that the adaptive significance of female copying may depend primarily on the ratio of the costs to the benefits of active mate choice. Copying behavior, and more generally conspecific cueing, may be important in many behavioral processes beyond mate choice.
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Dugatkin, L. A., & Godin, G. J. (1992). Predator inspection, shoaling and foraging under predation hazard in the Trinidadian guppy,Poecilia reticulata. Environmental Biology of Fishes, 34(3), 265–276.
Abstract: Guppies,Poecilia reticulata, living in stream pools in Trinidad, West Indies, approached a potential fish predator (a cichlid fish model) in a tentative, saltatory manner, mainly as singletons or in pairs. Such behavior is referred to as predator inspection behavior. Inspectors approached the trunk and tail of the predator model more frequently, more closely and in larger groups than they approached the predator's head, which is presumably the most dangerous area around the predator. However, guppies were not observed in significantly larger shoals in the stream when the predator model was present. In a stream enclosure, guppies inspected the predator model more frequently when it was stationary compared to when it was moving, and made closer inspections to the posterior regions of the predator than to its head. Therefore, the guppies apparently regarded the predator model as a potential threat and modified their behavior accordingly when inspecting it. Guppies exhibited a lower feeding rate in the presence of the predator, suggesting a trade-off between foraging gains and safety against predation. Our results further suggest that predator inspection behavior may account for some of this reduction in foraging. These findings are discussed in the context of the benefits and costs of predator inspection behavior.
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Kacelnik, A., & Todd, I. A. (1992). Psychological mechanisms and the Marginal Value Theorem: effect of variability in travel time on patch exploitation. Anim. Behav., 43(2), 313–322.
Abstract: The Marginal Value Theorem (MVT) describes the behaviour that maximizes the ratio of expected gain over expected foraging time in a patchy environment. When travel time is variable, the MVT rationale and its predictions are sensitive only to the mean travel time and not to the spread or skew of the distribution. Two mechanistic arguments contradict these predictions. First, tests of the MVT have previously shown that there is a disproportionate influence of the last travel time, and second, psychological models of information processing suggest that memory for time intervals is strongly dependent on the scatter of the distribution experienced. These mechanistic concepts, combined with Jensen's inequality, suggest that patch exploitation should decrease as the scatter of the travel distribution increases. In a Skinner box experiment with pigeons, Columba livia, the problem was examined by simulating three environments with identical patches and the same mean travel time, but different travel time variability. Patch exploitation decreased with increasing variance in travel time. The results are used to argue in favour of the inclusion of realistic psychological properties as constraints in functional models of behaviour. Although both the MVT and the mechanistic models account for some features of the results, none of them can explain all the findings.
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Caraco, T., Kacelnik, A., Mesnick, N., & Smulewitz, M. (1992). Short-term rate maximization when rewards and delays covary. Anim. Behav., 44(Part 3), 441–447.
Abstract: In nature foragers must exploit resources that vary randomly in both the energy acquired per item (reward) and the time required to pursue, capture and process an item (delay). Furthermore, rewards and delays associated with particular resources may often covary significantly. An analytical model asks how variance-covariance levels for rewards and delays could influence choice of resources when lack of information or cognitive limitation implies that a consumer attempts to maximize its short-term rate of energy gain. Both greater expected reward and reduced expected delay clearly should enhance preference for a resource. The model predicts that increased delay variance and reduced reward-delay covariance should increase a forager's preference for a resource. A forager should be risk-averse towards reward variance when the reward-delay covariance is positive, but should become risk-prone towards reward variance when the reward-delay covariance is negative.
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Brunner, D., Kacelnik, A., & Gibbon, J. (1992). Optimal foraging and timing processes in the starling, Sturnus vulgaris: effect of inter-capture interval. Anim. Behav., 44(4), 597–613.
Abstract: Laboratory experiments with starlings, Sturnus vulgaris, were conducted to investigate the interaction between timing and cost-benefit considerations. The design simulated an environment in which food was distributed in patches. Patches contained a random number of food items (N=0-4) separated by a fixed inter-capture interval or fixed interval. All patches ended with sudden depletion. The time elapsed since the last prey capture was the only way to detect the depletion of the patch. Once the patch was depleted a new patch could be reached by travelling between two perches. Three measures of timing were taken: (1) rate of working for food as function of `waiting' time in a patch, (2) the time of the last response in a patch or `giving-in' time, and (3) the time at which travel was initiated or `moving-on' time. The fixed interval that characterized patches was varied between conditions. The mean time of the peak in working rate was consistently centred around the fixed interval, while the other two measures of timing kept a roughly linear relation to the fixed interval, with slope greater than one. In accordance with Scalar Expectancy Theory, variability in the three forms of timing was proportional to the magnitude of the fixed interval. The birds seemed to take account of this increase in variability as shown by the mean value of their giving-up criterion. These results imply that information-processing constraints are important for modelling behavioural optimality.
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Kabuga, J. D. (1992). Social relationships in N'dama cattle during supplementary feeding. Appl. Anim. Behav. Sci., 34(4), 285–290.
Abstract: Social relationships of 30 N'dama cows during supplementary feeding, post-grazing, were studied over a period of 1.5 years. Dominance ranks determined during idling and feeding periods were strongly correlated (Spearman's rank correlation (rs = 0.964, P < 0.01). The number of animals dominated by a cow during feeding was strongly (P < 0.01) related to liveweight (r = 0.822) and age (r = 0.755). Low status cows ate less frequently than medium and high status animals, while middle ranking cows were ejected more frequently from the feed trough than other dominance groups. Animals had preferences in the use of feed troughs, with social rank being the dominant factor determining the location of feed trough space used. Cows of similar status were generally preferred feeding and movement neighbours and antagonists. However, the dominance rank of an animal and its preferred neighbour during idling were not significantly correlated (rs = 0.220, P > 0.05). Voluntary leadership ranks into and out of the pen were, respectively, related closely (P < 0.01) to feeding dominance ranks (rs = 0.661, 0.640) and idling dominance ranks (rs = 0.621, 0.669).
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Harkins, J. D., Kamerling, S. G., & Church, G. (1992). Effect of competition on performance of thoroughbred racehorses. J Appl Physiol, 72(3), 836–841.
Abstract: The effect of competition and the influence of age and sex on performance were examined in a study of 18 Thoroughbred racehorses. The horses performed two solo and two competitive runs at 1,200 and 1,600 m for a total of eight runs. No group ran faster during competition, which may have been a reflection of the quality of horses used for this study and their susceptibility to stress-induced impairment of performance. Males showed no significant difference between competitive and solo run times, whereas females were consistently slower during competition. Males ran significantly faster than females in all runs. There was no difference in run times due to age, which may have been due to the high mean age (5.9 yr) of the group. The slower competitive run times may have occurred because of an earlier onset of fatigue when compared with solo runs. Plasma lactate was significantly greater for the 1,200-m competitive than for the solo runs.
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Dugatkin, L. A., & Godin, J. G. (1992). Reversal of female mate choice by copying in the guppy (Poecilia reticulata). Proc Biol Sci, 249(1325), 179–184.
Abstract: Ever since Fisher (1958) formalized models of sexual selection, female mate choice has been assumed to be a genetically determined trait. Females, however, may also use social cues to select mates. One such cue might be the mate choice of conspecifics. Here we report the first direct evidence that a female's preference for a particular male can in fact be reversed by social cues. In our experiments using the Trinidadian guppy (Poecilia reticulata), this reversal was mediated by mate-copying opportunities, such that a female (the 'focal' female) is given the opportunity to choose between two males, followed by a period in which she observes a second female (the 'model' female) displaying a preference for the male she herself did not prefer initially. When allowed to choose between the same males a second time, compared with control tests, a significant proportion of focal females reversed their mate choice and copied the preference of the model female. These results provide strong evidence for the role of non-genetic factors in sexual selection and underlie the need for new models of sexual selection that explicitly incorporate both genetic and cultural aspects of mate choice.
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