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Coleman, K.; Wilson, D.S. |
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Title |
Shyness and boldness in pumpkinseed sunfish: individual differences are context-specific |
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Journal Article |
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1998 |
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Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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56 |
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4 |
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927-936 |
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Abstract |
Natural selection often promotes a mix of behavioural phenotypes in a population. Adaptive variation in the propensity to take risks might explain individual differences in shyness and boldness in humans and other species. It is often implicitly assumed that shyness and boldness are general personality traits expressed across many situations. From the evolutionary standpoint, however, individual differences that are adaptive in one context (e.g. predator defence) may not be adaptive in other contexts (e.g. exploration of the physical environment or intraspecific social interactions). We measured the context specificity of shyness and boldness in a natural population of juvenile pumpkinseed sunfish,Lepomis gibbosus, by exposing the fish to a potentially threatening stimulus (a red-tipped metrestick extended towards the individual) and a nonthreatening stimulus (a novel food source). We also related these measures of shyness and boldness to behaviours observed during focal observations, both before and after the introduction of a predator (largemouth bass,Micropterus salmoides). Consistent individual differences were found within both contexts, but individual differences did not correlate across contexts. Furthermore, fish that were scored as intermediate in their response to the metrestick behaved most boldly as foragers and in response to the bass predators. These results suggest that shyness and boldness are context-specific and may not exist as a one-dimensional behavioural continuum even within a single context. |
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2094 |
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Author |
Caraco, T.; Kacelnik, A.; Mesnick, N.; Smulewitz, M. |
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Title |
Short-term rate maximization when rewards and delays covary |
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Journal Article |
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Year |
1992 |
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Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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44 |
Issue |
Part 3 |
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441-447 |
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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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2113 |
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Palagi, E. |
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Title |
Sharing the motivation to play: the use of signals in adult bonobos |
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Journal Article |
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2008 |
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Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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75 |
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3 |
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887-896 |
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bonobo; full play face; Pan paniscus; play face; playful propensity; ritualization; social play; social tolerance; solitary play; visual communication |
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Gestures and facial displays are involved in regulating many aspects of mammal social life such as aggression, dominance-subordinate relationships, appeasement and play. Playful activity is an interesting behaviour for examining the role of signals as intentional communication systems. When animals play they perform patterns that are used in other serious contexts. To avoid miscommunication, many species have evolved signals to maintain a playful mood. Bonobos, Pan paniscus, with their flexible social relationships and playful propensity, may represent a good model species to test some hypotheses on adult play signalling. I analysed the potential roles of facial play expressions and solitary play in soliciting and regulating social play and found that adult bonobos used the play face (relaxed open-mouth display) in a selective manner. Play faces were more frequent during social than solitary play and, within social play, polyadic sessions (even though less frequent than dyadic sessions) were characterized by a higher frequency of signals. Following the rule of play intensity matching, play faces were more frequent when the two players matched in age and size (sessions among adults). Moreover, among dyads there was a positive correlation between the frequency of aggressive interactions performed and the frequency of play signals used, thus suggesting that signals are crucial in play negotiations among individuals showing high baseline levels of aggression. Finally, solitary play, especially when it involved pirouettes and somersaults, had an important role in triggering social play. |
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Equine Behaviour @ team @ |
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4316 |
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Author |
Clutton-Brock, T.H.; Parker, G.A. |
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Title |
Sexual coercion in animal societies |
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Journal Article |
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Year |
1995 |
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Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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Volume |
49 |
Issue |
5 |
Pages |
1345-1365 |
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In a wide range of animal species, males coerce females to mate with them, either by physically forcing them to mate, by harassing them until they mate or by punishing persistent refusal to mate. The first section of this paper argues that the possibility of forced copulation can generate arms races between males and females that may have substantial costs to both sexes. In the second section, it is suggested that sexual harassment commonly represents a `war of attrition' between the sexes; existing game theory models that may apply to sexual conflict over mating decisions are reviewed. The third section develops a simple prospective model for the evolution of intimidation by punishment in situations where males can raise the probability that females will accept their advances in future by punishing them for refusal to mate. Where the benefits of sexual coercion to males are high, all three male strategies may develop to a point where they have substantial costs to females. In the final section, evidence that female behaviour is adapted to minimizing these costs is reviewed. |
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refbase @ user @ |
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757 |
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Powell, A.J.; Wolff, P.R. |
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Title |
Sex differences in mouse urination patterns |
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Journal Article |
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Year |
1982 |
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Animal Behaviour. |
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Anim. Behav. |
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30 |
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4 |
Pages |
1207-1211 |
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When tested in circular open fields male and female mice (Mus musculus) produced strongly centrifugal urination patterns, which showed a clear `edge-dependency' in all the field sizes used. However, striking sex differences in the pattern of deposition were shown in terms of both the number and distribution of the urine spots. Male mice produce large numbers of spots which are regularly dispersed, while females produce relatively fewer spots with a more clumped distribution. It is suggested that a hitherto unsuspected level of intersexual communication may explain these differences. |
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2145 |
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Author |
Mitchell R |
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Title |
Self-recognition, methodology and explanation: a comment on Heyes (1994) |
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Journal Article |
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Year |
1995 |
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Animal Behaviour. |
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Anim. Behav. |
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51 |
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467 |
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Equine Behaviour @ team @ |
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3020 |
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Author |
Anderson JR; Gallup GG |
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Title |
Self-recognition in Saguinus? A critical essay |
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1997 |
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Animal Behaviour. |
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Anim. Behav. |
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54 |
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1563 |
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Equine Behaviour @ team @ |
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2978 |
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Author |
Heyes CM |
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Title |
Self-recognition in primates: irreverence, irrelevance and irony |
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1996 |
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Animal Behaviour. |
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Anim. Behav. |
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51 |
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470 |
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Equine Behaviour @ team @ |
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3007 |
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Heyes CM |
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Title |
Self-recognition in primates: further reflections create a hall of mirrors |
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1995 |
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Animal Behaviour. |
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Anim. Behav. |
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50 |
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1533 |
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Equine Behaviour @ team @ |
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3006 |
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Goldschmidt, T.; Bakker, T.C.M.; Feuth-de Bruijn, E. |
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Title |
Selective copying in mate choice of female sticklebacks |
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Journal Article |
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1993 |
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Animal Behaviour. |
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Anim. Behav. |
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45 |
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3 |
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541-547 |
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There is evidence that female three-spined sticklebacks, Gasterosteus aculeatus L., prefer to mate with males whose nests contain eggs rather than with males with empty nests. While there is consensus on this point, a dispute exists about whether this preference should be attributed to a direct effect of the eggs on the female's entering the nest or, alternatively, to a positive impact of the eggs on the courtship behaviour and breeding coloration of the male. In the field experiment reported here females strongly preferred nests with eggs over empty nests. Additionally, females were less likely to enter risky nests with eggs: nests that contained fewer eggs than one average clutch or more eggs than the average nest content of parental males in this population. However, in the field possible differences in male attractiveness were not controlled for. In supplementary laboratory experiments the effect on female choice of possible changes in male attractiveness (intensified courtship and coloration) as a result of the presence of eggs in the nest was tested. Other differences in male attractiveness as a result of differences in male quality (body size, breeding coloration before the test, territory quality and size) were controlled for. When females had no access to the nests, they showed no preference for males with eggs in their nests in simultaneous choice tests. These results, together with the earlier published data, make it likely that the preference of females for nests with eggs is partly a direct consequence of the eggs themselves. So female sticklebacks are influenced by the mate choice behaviour of other females, but remain selective as to the actual nest content. |
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1818 |
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