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Focal Individual (focal + individual)
Selected AbstractsCorrelates of Self-Directed Behaviour in Wild White-Faced CapuchinsETHOLOGY, Issue 4 2000Joseph H. Manson Elevated rates of self-directed behaviour (SDB) such as self-scratching and autogrooming have been widely used in recent years as an indicator of anxiety in catarrhine primates. This study presents the first examination of correlates of SDB rates in a platyrrhine primate. Subjects were 8 wild female white-faced capuchins at Lomas Barbudal, Costa Rica, who were observed for 119 h of focal individual follows. The subjects performed significantly more self-scratching and autogrooming while in close proximity to conspecifics than while alone, irrespective of whether the neighbour was dominant or subordinate to them. This result was attributable to elevated SDB rates during the 30 s preceding and following allogrooming bouts. Furthermore, subjects engaged in more SDB while in proximity to females (a) that were closer to them in dominance rank and (b) with whom they spent a larger proportion of their time in proximity. Self-directed behaviour rates after conflicts did not differ from non-postconflict rates. Nor were SDB rates above baseline levels during the 30 s before subjects descended to the ground. These results may provide support for the view that SDB rates index anxiety in this species, if grooming decisions signal individuals' current allegiances and are therefore a source of anxiety, even if being groomed is, itself, relaxing. Postconflict preparation for further aggression may mitigate against scratching and autogrooming in a fast-moving arboreal species. [source] INDIRECT GENETIC EFFECTS INFLUENCE ANTIPREDATOR BEHAVIOR IN GUPPIES: ESTIMATES OF THE COEFFICIENT OF INTERACTION PSI AND THE INHERITANCE OF RECIPROCITYEVOLUTION, Issue 7 2009Bronwyn H. Bleakley How and why cooperation evolves, particularly among nonrelatives, remains a major paradox for evolutionary biologists and behavioral ecologists. Although much attention has focused on fitness consequences associated with cooperating, relatively little is known about the second component of evolutionary change, the inheritance of cooperation or reciprocity. The genetics of behaviors that can only be expressed in the context of interactions are particularly difficult to describe because the relevant genes reside in multiple social partners. Indirect genetic effects (IGEs) describe the influence of genes carried in social partners on the phenotype of a focal individual and thus provide a novel approach to quantifying the genetics underlying interactions such as reciprocal cooperation. We used inbred lines of guppies and a novel application of IGE theory to describe the dual genetic control of predator inspection and social behavior, both classic models of reciprocity. We identified effects of focal strain, social group strain, and interactions between focal and group strains on variation in focal behavior. We measured ,, the coefficient of the interaction, which describes the degree to which an individual's phenotype is influenced by the phenotype of its social partners. The genetic identity of social partners substantially influences inspection behavior, measures of threat assessment, and schooling and does so in positively reinforcing manner. We therefore demonstrate strong IGEs for antipredator behavior that represent the genetic variation necessary for the evolution of reciprocity. [source] The evolution of cooperation and altruism , a general framework and a classification of modelsJOURNAL OF EVOLUTIONARY BIOLOGY, Issue 5 2006L. LEHMANN Abstract One of the enduring puzzles in biology and the social sciences is the origin and persistence of intraspecific cooperation and altruism in humans and other species. Hundreds of theoretical models have been proposed and there is much confusion about the relationship between these models. To clarify the situation, we developed a synthetic conceptual framework that delineates the conditions necessary for the evolution of altruism and cooperation. We show that at least one of the four following conditions needs to be fulfilled: direct benefits to the focal individual performing a cooperative act; direct or indirect information allowing a better than random guess about whether a given individual will behave cooperatively in repeated reciprocal interactions; preferential interactions between related individuals; and genetic correlation between genes coding for altruism and phenotypic traits that can be identified. When one or more of these conditions are met, altruism or cooperation can evolve if the cost-to-benefit ratio of altruistic and cooperative acts is greater than a threshold value. The cost-to-benefit ratio can be altered by coercion, punishment and policing which therefore act as mechanisms facilitating the evolution of altruism and cooperation. All the models proposed so far are explicitly or implicitly built on these general principles, allowing us to classify them into four general categories. [source] Neighbor effects in marmosets: social contagion of agonism and affiliation in captive Callithrix jacchusAMERICAN JOURNAL OF PRIMATOLOGY, Issue 6 2010Claire F.I. Watson Abstract Researchers have demonstrated the neighbor effect for affiliative and agonistic neighbor vocalizations in captive chimpanzees. We extend the investigation of the neighbor effect to New World monkeys, Callithrix jacchus. We collected data on vocalizations and behaviors of 31 focal individuals and concurrent neighbor vocalization within three behavioral categories: intragroup and intergroup aggression and intragroup affiliation. We investigated whether there was an influence of neighbor vocalizations on focal behavior within the same behavioral category. For data analysis we used approximate randomization of paired-sample t -tests. We found that marmosets performed intergroup aggressive behavior (bristle, anogenital present for neighbor loud shrill only) for significantly longer, and emitted significantly more intergroup agonistic vocalizations (twitter, loud shrill), at a high frequency of intergroup agonistic neighbor vocalizations (twitter, loud shrill) than at low. The marmosets were also significantly more likely to engage in bristle behavior immediately after hearing a neighbor intergroup aggressive call (twitter, loud shrill) than directly beforehand. High neighbor intragroup agonistic calls (chatter) were associated with significantly longer spent in related behavior (composite of: attack, chase, steal food). Affiliative behaviors (share food, grooming invite) were engaged in by marmosets for significantly longer at higher frequencies of affiliative neighbor chirp calls than at low. Marmosets were also significantly more likely to perform food sharing and active affiliative contact immediately after rather than before hearing a neighbor chirp call. Our findings suggest that neighbor vocalizations influence marmoset behavior through social contagion and indicate that the neighbor effect for affiliation and aggression generalizes to the marmoset. Am. J. Primatol. 72:549,558, 2010. © 2010 Wiley-Liss, Inc. [source] Individual variation in nest size and nest site features of the Bornean orangutans (Pongo pygmaeus)AMERICAN JOURNAL OF PRIMATOLOGY, Issue 5 2009Yaya Rayadin Abstract Nest construction is a daily habit of independent orangutans for sleeping or resting. Data on their nests have been used in various ecological studies (e.g., density estimation, ranging behavior, evolution of material culture) because they are the most observable field signs. We investigated nest size and nest site features of Bornean orangutans in the wild during 10 months' fieldwork at three sites in East Kalimantan, Indonesia: Kutai National Park, Birawa, and Meratus. To examine individual variation, we followed 31 individual orangutans and recorded the 92 nests they made for nest size (diameter) and nest site features (height of nest above ground, tree species used for the nest site, the diameter and height of the tree, whether the nest was new or reused, and nest location within the tree). Analyses taking age,sex classes of the focal individuals into consideration showed significant age,sex differences in nest size and location, but not in nest height or nest tree features (diameter, height of tree, and height of lowest branch). Mature orangutans (adult females, unflanged and flanged males) made larger nests than immatures (juveniles and adolescents). Flanged male orangutans with larger nests used stable locations for nesting sites and reused old nests more frequently than immatures. The overall proportion of nests in open (exposed) locations was higher than in closed (sheltered) locations. Flanged males and immatures frequently made open nests, whereas adult females with an infant preferred closed locations. The good correspondence between nest size and age,sex classes indicates that nest size variation may reflect body size and therefore age,sex variation in the population. Am. J. Primatol. 71:393,399, 2009. © 2009 Wiley-Liss, Inc. [source] | ||||||||||