Jennings, D. J., Carlin, C. M., & Gammell, M. P. (2009). A winner effect supports third-party intervention behaviour during fallow deer, Dama dama, fights. Anim. Behav., 77(2), 343–348.
Abstract: Male ungulates engage in intense competition for access to females during the breeding season. Although fights are generally dyadic level encounters, they are on occasion disrupted by the intervention of third-party males. We investigated these third-party interventions using predictions derived from Dugatkin's model (Dugatkin 1998, Proceedings of the Royal Society of London, Series B, 265, 433-437) of intervention behaviour. The model argues that when an individual successfully defeats an opponent there is an increase in the probability of winning a subsequent contest: a winner effect. Third-party intervention behaviour is predicted to occur as it serves to prevent either member of a competing dyad from successfully defeating his opponent, achieving a winner effect and subsequently becoming a threat to the intervener. Consistent with model predictions, our results show that intervening males held significantly higher rank than males that did not intervene and were also more likely to be dominant to both of the competing males. Intervening males did not selectively target competitors based on rank, nor did they target males based on overall dyadic rates of aggression between the intervener and competing males. Furthermore, interveners were more likely to have won their interaction immediately prior to intervention and were also likely to win their interaction subsequent to intervention when compared with contest success of the two competing males. Our results are consistent with predictions that support a winner effect for intervention behaviour in fallow deer fights.
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Parker, G. A., & MacNair, M. R. (1978). Models of parent-offspring conflict. I. Monogamy. Anim. Behav., 26, 97–110.
Abstract: Theoretical models for Trivers (1974) concept of parent-offspring conflict are examined for species in which the effects of the conflict are felt by full sibs. A rare conflictor gene will spread if Image , whereÆ’(m) is the fitness gained by a conflictor relative to a non-conflictor offspring (Æ’(m) >1), and m is the amount of parental investment taken by a conflictor relative to m = 1 for a non-conflictor. The range of m alleles which can spread against the parent optimum decreases as the cost to the parent increases until a point is reached where there is no conflict of evolutionary interests. There would be no polymorphism for conflictor: non-conflictor alleles unless special conditions prevail. The conflictor allele which spreads most rapidly as a rare mutant against the parental optimum is not an evolutionarily stable strategy (ESS). The ESS for parent-offspring conflict in monogamous species has m0 = Æ’(m0)/2[dÆ’(m0)/dm0]. The analytical solutions are confirmed throughout by simulations.
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Mulder, R. A., & Langmore, N. E. (1993). Dominant males punish helpers for temporary defection in superb fairy-wrens. Anim. Behav., 45, 830–833.
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Manson, J. H. (1992). Measuring female mate choice in Cayo Santiago rhesus macaques. Anim. Behav., 44, 405–416.
Abstract: Few studies of female mate choice have been carried out among free-ranging non-human primates. To qualify as female mate choice, behaviour by oestrous females must predict the occurrence or rate of potentially fertile copulations, in comparisons between heterosexual dyads. In this paper, data are presented to show three behaviour patterns that meet this criterion in free-ranging rhesus macaques, Macaca mulatta, at the island colony of Cayo Santiago: (1) selective cooperation with male sexual solicitations (hip-grasps), (2) restoration of proximity following attacks on females by intruding males, and (3) proximity maintenance (in one of two study groups). Oestrous females maintained proximity preferentially to lower ranking males, but this appeared to reflect differences in the tactics necessary to achieve copulations with males of different dominance ranks, rather than preference for lower ranking mates. Male-oestrous female dyads showed consistency over two consecutive mating seasons in which partner was responsible for proximity maintenance. Male dominance rank was positively correlated with copulatory rate with fertile females. However, in one study group, males to whom oestrous females maintained proximity more actively had higher copulatory rates with fertile females, independent of the effects of male dominance rank.
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Manson, J. H. (1994). Male aggression: a cost of female mate choice in Cayo Santiago rhesus macaques. Anim. Behav., 48, 473–475.
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Cheney, D. L., & Seyfarth, R. M. (1986). The recognition of social alliances among vervet monkeys. Anim. Behav., 34, 1722–1731.
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Aureli, F., Cossolino, R., Cordischi, C., & Scucchi, S. (1992). Kin-oriented redirection among Japanese macaques: an expression of a revenge system? Anim. Behav., 44(2), 283–291.
Abstract: The ability to recognize the close associates of other group members may permit the display of redirected aggression against the relatives of the former aggressor. However, the dominance structure and the kin-based alliance system of macaque society are expected not to favour the occurrence of this kin-oriented redirection. Nevertheless, within 1 h of being the victim of an attack, Japanese macaques, Macaca fuscata, were more likely to attack the former aggressor's kin than without such a conflict. The conditions under which the victim redirected against the former aggressor's kin were investigated. This kin-oriented redirection did not occur preferentially either after conflicts between individuals with unstable and/or uncertain dominance relationships or after conflicts with individuals that were unlikely to intervene in favour of their kin. Victims redirected against individuals that were younger than the former aggressor and often subordinate to the victim. They also redirected in an opportunistic way by joining polyadic interactions against the former aggressor's kin. The possibility that this kin-oriented redirection may have a long-term function in changing the aggressive attitude of the aggressor towards the victim is also discussed. In addition, the victim's kin also displayed a form of kin-oriented redirection. They were more likely to attack the kin of an individual after it had attacked their own kin.
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Lefebvre, L., Whittle, P., Lascaris, E., & Finkelstein, A. (1997). Feeding innovations and forebrain size in birds. Anim. Behav., 53(3), 549–560.
Abstract: The links between ecology, behavioural plasticity and brain size are often tested via the comparative method. Given the problems in interpretating comparative tests of learning and cognition, however, alternative measures of plasticity need to be developed. From the short notes section of nine ornithological journals, two separate, exhaustive data sets have been collated on opportunistic foraging innovations in birds of North America (1973-1993;N=196) and the British Isles (1983-1993;N=126). Both the absolute and relative frequencies (corrected for species number per order) of innovations differ between bird orders in a similar fashion in the two geographical zones. Absolute and relative frequency of innovations per order are also related to two measures of relative forebrain size in the two zones. The study confirms predicted trends linking opportunism, brain size and rate of structural evolution. It also suggests that innovation rate in the field may be a useful measure of behavioural plasticity.
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Kudo, H., & Dunbar, R. I. M. (2001). Neocortex size and social network size in primates. Anim. Behav., 62(4), 711–722.
Abstract: Primates use social grooming to service coalitions and it has been suggested that these directly affect the fitness of their members by allowing them to reduce the intrinsic costs associated with living in large groups. We tested two hypotheses about the size of grooming cliques that derive from this suggestion: (1) that grooming clique size should correlate with relative neocortex size and (2) that the size of grooming cliques should be proportional to the size of the groups they have to support. Both predictions were confirmed, although we show that, in respect of neocortex size, there are as many as four statistically distinct grades within the primates (including humans). Analysis of the patterns of grooming among males and females suggested that large primate social groups often consist of a set of smaller female subgroups (in some cases, matrilinearly based coalitions) that are linked by individual males. This may be because males insert themselves into the interstices between weakly bonded female subgroups rather than because they actually hold these subunits together.
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Boesch, C. (1994). Cooperative hunting in wild chimpanzees. Anim. Behav., 48(3), 653–667.
Abstract: A model for the evolution of cooperation shows that two conditions are necessary for cooperation to be stable: a hunting success rate that is low for single hunters and increases with group size, and a social mechanism limiting access to meat by non-hunters. Testing this model on TaI chimpanzees, Pan troglodytes, showed that (1) it pays for individuals to hunt in groups of three or four rather than alone or in pairs, and (2) cooperation is stable because hunters gain more at these group sizes than cheaters, owing to a meat-sharing pattern in which hunting, dominance and age, in that order, determine how much an individual gets. In addition, hunters provide cheaters (about 45% of the meat eaters) with the surplus they produce during the hunts. Thus, cooperation in Tai male chimpanzees is an evolutionarily stable strategy, and its success allows cheating to be an evolutionarily stable strategy for Tai female chimpanzees. In Gombe chimpanzees, cooperation is not stable, first, because hunting success is very high for single hunters, and second, because no social mechanism exists that limits access to meat by non-hunters. The analysis showed that some assumptions made when discussing cooperation in other social hunters might be wrong. This might downgrade our general perception of the importance of cooperation as an evolutionary cause of sociality.
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