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Witte, K., & Ryan, M. J. (2002). Mate choice copying in the sailfin molly, Poecilia latipinna, in the wild. Anim. Behav., 63(5), 943–949.
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Slagsvold, T., & Viljugrein, H. (1999). Mate choice copying versus preference for actively displaying males by female pied flycatchers. Anim. Behav., 57(3), 679–686.
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White, D. J., & Galef Jr, B. G. (1999). Mate choice copying and conspecific cueing in Japanese quail,Coturnix coturnix japonica. Anim. Behav., 57(2), 465–473.
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Dugatkin, L. A. (1998). A comment on Lafleur et al.'s re-evaluation of mate-choice copying in guppies. Anim. Behav., 56(2), 513–514.
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Hoglund, J., Alatalo, R. V., Gibson, R. M., & Lundberg, A. (1995). Mate-choice copying in black grouse. Anim. Behav., 49(6), 1627–1633.
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Richards, S. A., & de Roos, A. M. (2001). When is habitat assessment an advantage when foraging? Anim. Behav., 61(6), 1101–1112.
Abstract: Foragers can often show a broad range of strategies when searching for resources. The simplest foraging strategy is to search randomly within a habitat; however, foragers can often assess habitat quality over various spatial scales and use this information to keep themselves in, or direct themselves to, regions of high resource abundance or low predation risk. We investigated models that describe a population of consumers competing for a renewable resource that is distributed among discrete patches. Our aim was to identify what foraging strategy or strategies are expected to persist within a population, where strategies differ in the degree of habitat assessment (i.e. none, local, or global). We were interested in how the optimal strategies are dependent on the cost of assessment and habitat structure (i.e. the variation in renewal rates and predation risks among patches). The models showed that the simple random foraging strategy (i.e. make no habitat assessments) often persisted even when the cost of habitat assessment was low. Persistence could occur when habitat assessment and population dynamics generated an ideal free distribution because it could be exploited by the random foragers. Habitat assessment was more advantageous when consumers could not achieve ideal free distributions, which was more likely as patches became less productive. When productivity was low we sometimes observed the situation where different foraging strategies generated resource heterogeneities that promoted their coexistence, and this could occur even when all patches were intrinsically identical.
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Richards, M. P. M. (1966). Maternal behaviour in virgin female golden hamsters (Mesocricetus auratus waterhouse): the role of the age of the test pup. Anim. Behav., 14(2-3), 303–309.
Abstract: Summary One hundred and forty-four naive virgin female golden hamsters were each given a single 15 min test with three pups aged from day 1 (<24 hr) to day 18. A group of eight females was tested with each age of pup. Pups aged from day 1 to day 6 were generally attacked like prey, killed and eaten. Pups of intermediate age (day 6 to day 10) were usually initially attacked but this was often followed by maternal responses. The females', behaviour with the oldest pups suggested that they were being treated as strnge adult intruders. This result differs from that of a similar experiment with mice in which the youngest pups were found to be the most effective for eliciting materal responses. An explanation for this difference in terms of the evolutionary history of the golden hamster species is proposed.
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Richards, M. P. M. (1966). Maternal behaviour in the golden hamster: responsiveness to young in virgin, pregnant, and lactating females. Anim. Behav., 14(2-3), 310–313.
Abstract: Summary Three groups of eight female golden hamsters without prior breeding experience were presented with three newborn pups for a 15 min test period. Group V were virgin females, group P pregnant females and group L lactating females. Groups P and L were tested within 24 hr of parturition. Group V attacked and killed all pups presented. Group P showed maternal responses after initial attacks while group L accepted the pups. Groups P and L did not differ significantly on measures of maternal responsiveness but all three groups differed significantly from one another on measures of attacking behaviour and the eating of young.
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Noirot, E., & Richards, M. P. M. (1966). Maternal behaviour in virgin female golden hamsters: Changes consequent upon initial contact with pups. Anim. Behav., 14(1), 7–10.
Abstract: Summary Initial contact with pups of a certain age causes changes in virgin female hamsters' behaviour with pups of another age. This was shown by comparing the behaviour with 5-day-old pups in groups of naive (control) animals and of animals given one previous contact either with 1, 5 or 9-day-old pups. Maternal responses were more intense in the animals previously presented with 1 or 9-day-old pups than in the control animals. Attacking was increased after initial contact with 1-day-old pups and decreased after initial contact with 9-day-old pups. Animals presented twice with the same pattern did not show marked changes in either of the two activities.
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Norris, M. J. (1962). Group effects on the activity and behaviour of adult males of the desert locust (Schistocerca gregaria Forsk.) in relation to sexual maturation. Anim. Behav., 10(3-4), 275–291.
Abstract: During the pre-maturation period crowded males of Schistocerca gregaria are more active than isolated ones but the greater part of their extra activity is not locomotory but consists of the kicking movements made in response to contact with other locusts. Isolated males walk less often during this period but tend to jump (or fly) more than crowded ones. Activity increases with maturity and the increase is greater in the isolated males so that in spite of the absence of mechanical stimulation by other locusts their locomotor activity is now at least as great as that of the crowded ones and their jumping activity greater. Within one batch there is a tendency for those males which are most active during the first two weeks of adult life to mature earliest. The activity of young males crowded with fledglings is at first similar to that of males crowded with older locusts, but after the first two weeks the activity of both mature and immature males is depressed by crowding with fledglings. Mature males habitually isolated become less active when temporarily crowded with fledglings, but not when crowded with mature males. Mature and immature males habitually crowded with fledglings become more active when temporarily isolated and still more active when crowded with each other, or with other mature males. The inhibiting effect of the fledglings on maturation and their depressive effect on activity should in natural conditions promote synchronization of maturation and the cohesion of the group. There was little difference in activity between young males kept in single pairs and in isolation, except that in one experiment the isolated ones jumped more often. Young males kept in pairs with mature males are more active during the first week of adult life than those kept in pairs with each other. The males paired with mature males were also seen feeding much less often than those paired with each other. This was the only treatment in which a significant effect on the frequency of feeding was recorded. The femoral vibrations made by both mature and immature males in response to stimulation by mature males, occur less often in habitually crowded males than in those temporarily crowded or kept with one mature male only. This is presumably the result of habituation to the stimulus. The behaviour of wild Schistocerca males in a large outdoor cage was very similar to that of a low density laboratory group. All results suggest that there is an association between high activity and rapid maturation. This is compatible with the conclusion from earlier work that a low level of feeding is associated with rapid maturation.
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