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Nowak, M. A., & Sigmund, K. (1992). Tit for tat in heterogeneous populations. Nature, 355, 250–253.
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Reeve, H. K. (1992). Queen activation of lazy workers in colonies of the eusocial naked mole-rat. Nature, 358, 147–149.
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Poysa, H. (1992). Group Foraging in Patchy Environments: The Importance of Coarse-Level Local Enhancement. Ornis[ Scand[, 23(2), 159–166.
Abstract: Local enhancement is one way individuals may realize foraging advantages from grouping. A distinction between fine-level and coarse-level local enhancement is made, the latter often being neglected in theoretical research on group foraging. In the former case, an individual has a higher feeding rate as a member of a group because individuals copy other group members' foraging, whereas in the latter, groups simply attract other individuals to patches where food is particularly abundant and copying does not occur within the group. Coarse-level local enhancement may decrease the time needed to find profitable feeding patches in spatially and temporally variable environments. A review of the empirical literature indicated that coarse-level local enhancement is typical in bird species foraging in open habitats and in large groups with relatively little competition between group members whereas the opposite attributes fit the species for which fine-level local enhancement had been documented. Furthermore, species in which coarse-level local enhancement prevails usually forage in temporary groups. However, coarse-level and fine-level local enhancement are not necessarily mutually exclusive, but which one is more important in a particular case may be habitat-dependent.
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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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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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Schmidt, D. (1992). Information Resources in Animal Behavior. Science & Technology Libraries, 12(1), 69–83.
Abstract: The study of animal behavior has been around for many years, but it is divided into several fields which often do not communicate well. These fields of study include (but are not limited to) comparative psychology, ethology, behavioral ecology, and sociobiology. Comparative psychology is more isolated than the other three fields, which share a common biological/evolutionary background. This paper gives a brief background of the four main fields of animal behavior research, along with a list of sources, both specialized and interdisciplinary.
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Seyfarth, R. M., & Cheney, D. L. (1992). Meaning and mind in monkeys. Sci Am, 267(6), 122–128.
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Elzenga, J. W.,. (1992). Why zebras are striped. Swara, 15(4), 28–30.
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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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Mills, M. G. L., & Shenk, M. G. L. (1992). Predator--Prey Relationships: The Impact of Lion Predation on Wildebeest and Zebra Populations. T. J. Anim. Ecol., 61(3), 693–702.
Abstract: 1. The role of lion Panthera leo predation in the dynamics of blue wildebeest Connochaetes taurinus and zebra Equus burchelli populations was investigated through simulation models. The data used in the models were from intensive observations over 4 years in the south-east of the Kruger National Park. 2. Population estimates of wildebeest and zebra were made from aerial surveys, sex and age ratios from ground counts. Lion numbers were determined from observations of marked and radio-collared animals. Predation was studied by following lions for continuous periods of up to 336 h. 3. Two models were constructed. Model 1 ascertained the number of killing lions (adult females) that could be supported by each prey population while remaining stable. A single model was constructed for the sedentary wildebeest population. A summer and winter model was constructed for the semi-migratory zebra population. The sensitivity of the parameters in the model was tested by changing their value by 10%. In model 2, the kill age structure for each species was changed to determine the number of killing lions the altered prey selection parameters could support. 4. There was no difference in the vulnerability of either species to predation. Zebra foals (<1 year) were killed more frequently than expected. No selection for sex or by season could be found for either species. 5. Model 1 predicted that the wildebeest population stabilizes with 7.7 killing lions, close to the number in the study area. The winter zebra population stabilizes with 6.8 killing lions and the summer zebra population with 19.4. Manipulation of kill rate followed by adult fecundity rate had the greatest effect on population size of both species. In model 2, wildebeest predation was made selective towards calves and zebra predation was made non-selective for sex and age. With these parameters the wildebeest population stabilizes with 10.7 killing lions and the zebra population with 5.4 in winter and 15.1 in summer. 6. The models suggest that lion predation affected wildebeest more severely than zebra during the study. This was through the way in which lions selected their prey, and because of the sedentary behaviour of the wildebeest, as opposed to the semi-migratory behaviour of the zebra.
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