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Ramos-Fernández, G., Boyer, D., Aureli, F., & Vick, L. (2009). Association networks in spider monkeys (Ateles geoffroyi). Behav. Ecol. Sociobiol., 63(7), 999-1013.
Abstract: We use two novel techniques to analyze association patterns in a group of wild spider monkeys (Ateles geoffroyi) studied continuously for 8 years. Permutation tests identified association rates higher or lower than chance expectation, indicating active processes of companionship and avoidance as opposed to passive aggregation. Network graphs represented individual adults as nodes and their association rates as weighted edges. Strength and eigenvector centrality (a measure of how strongly linked an individual is to other strongly linked individuals) were used to quantify the particular role of individuals in determining the network's structure. Female–female dyads showed higher association rates than any other type of dyad, but permutation tests revealed that these associations cannot be distinguished from random aggregation. Females formed tightly linked clusters that were stable over time, with the exception of immigrant females who showed little association with any adult in the group. Eigenvector centrality was higher for females than for males. Adult males were associated mostly among them, and although their strength of association with others was lower than that of females, their association rates revealed a process of active companionship. Female–male bonds were weaker than those between same-sex pairs, with the exception of those involving young male adults, who by virtue of their strong connections both with female and male adults, appear as temporary brokers between the female and male clusters of the network. This analytical framework can serve to develop a more complete explanation of social structure in species with high levels of fission–fusion dynamics.
Keywords: Biomedical and Life Sciences
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James, R., Croft, D., & Krause, J. (2009). Potential banana skins in animal social network analysis. Behav. Ecol. Sociobiol., 63(7), 989-997.
Abstract: Social network analysis is an increasingly popular tool for the study of the fine-scale and global social structure of animals. It has attracted particular attention by those attempting to unravel social structure in fission–fusion populations. It is clear that the social network approach offers some exciting opportunities for gaining new insights into social systems. However, some of the practices which are currently being used in the animal social networks literature are at worst questionable and at best over-enthusiastic. We highlight some of the areas of method, analysis and interpretation in which greater care may be needed in order to ensure that the biology we extract from our networks is robust. In particular, we suggest that more attention should be given to whether relational data are representative, the potential effect of observational errors and the choice and use of statistical tests. The importance of replication and manipulation must not be forgotten, and the interpretation of results requires care.
Keywords: Biomedical and Life Sciences
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Sih, A., Hanser, S., & McHugh, K. (2009). Social network theory: new insights and issues for behavioral ecologists. Behav. Ecol. Sociobiol., 63(7), 975–988.
Abstract: Abstract Until recently, few studies have used social network theory (SNT) and metrics to examine how social network structure (SNS) might influence social behavior and social dynamics in non-human animals. Here, we present an overview of why and how the social network approach might be useful for behavioral ecology. We first note four important aspects of SNS that are commonly observed, but relatively rarely quantified: (1) that within a social group, differences among individuals in their social experiences and connections affect individual and group outcomes; (2) that indirect connections can be important (e.g., partners of your partners matter); (3) that individuals differ in their importance in the social network (some can be considered keystone individuals); and (4) that social network traits often carry over across contexts (e.g., SN position in male–male competition can influence later male mating success). We then discuss how these four points, and the social network approach in general, can yield new insights and questions for a broad range of issues in behavioral ecology including: mate choice, alternative mating tactics, male–male competition, cooperation, reciprocal altruism, eavesdropping, kin selection, dominance hierarchies, social learning, information flow, social foraging, and cooperative antipredator behavior. Finally, we suggest future directions including: (1) integrating behavioral syndromes and SNT; (2) comparing space use and SNS; (3) adaptive partner choice and SNS; (4) the dynamics and stability (or instability) of social networks, and (5) group selection shaping SNS.
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Krause, J., Lusseau, D., & James, R. (2009). Animal social networks: an introduction. Behav. Ecol. Sociobiol., 63(7), 967-973.
Abstract: Network analysis has a long history in the mathematical and social sciences and the aim of this introduction is to provide a brief overview of the potential that it holds for the study of animal behaviour. One of the most attractive features of the network paradigm is that it provides a single conceptual framework with which we can study the social organisation of animals at all levels (individual, dyad, group, population) and for all types of interaction (aggressive, cooperative, sexual etc.). Graphical tools allow a visual inspection of networks which often helps inspire ideas for testable hypotheses. Network analysis itself provides a multitude of novel statistical tools that can be used to characterise social patterns in animal populations. Among the important insights that networks have facilitated is that indirect social connections matter. Interactions between individuals generate a social environment at the population level which in turn selects for behavioural strategies at the individual level. A social network is often a perfect means by which to represent heterogeneous relationships in a population. Probing the biological drivers for these heterogeneities, often as a function of time, forms the basis of many of the current uses of network analysis in the behavioural sciences. This special issue on social networks brings together a diverse group of practitioners whose study systems range from social insects over reptiles to birds, cetaceans, ungulates and primates in order to illustrate the wide-ranging applications of network analysis.
Keywords: Biomedical and Life Sciences
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Hampton, R. R., & Shettleworth, S. J. (1996). Hippocampus and memory in a food-storing and in a nonstoring bird species. Behav Neurosci, 110(5), 946–964.
Abstract: Food-storing birds maintain in memory a large and constantly changing catalog of the locations of stored food. The hippocampus of food-storing black-capped chickadees (Parus atricapillus) is proportionally larger than that of nonstoring dark-eyed juncos (Junco hyemalis). Chickadees perform better than do juncos in an operant test of spatial non-matching-to-sample (SNMTS), and chickadees are more resistant to interference in this paradigm. Hippocampal lesions attenuate performance in SNMTS and increase interference. In tests of continuous spatial alternation (CSA), juncos perform better than chickadees. CSA performance also declines following hippocampal lesions. By itself, sensitivity of a given task to hippocampal damage does not predict the direction of memory differences between storing and nonstoring species.
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Koolhaas, J. M., Korte, S. M., De Boer, S. F., Van Der Vegt, B. J., Van Reenen, C. G., Hopster, H., et al. (1999). Coping styles in animals: current status in behavior and stress-physiology. Neuroscience & Biobehavioral Reviews, 23(7), 925–935.
Abstract: This paper summarizes the current views on coping styles as a useful concept in understanding individual adaptive capacity and vulnerability to stress-related disease. Studies in feral populations indicate the existence of a proactive and a reactive coping style. These coping styles seem to play a role in the population ecology of the species. Despite domestication, genetic selection and inbreeding, the same coping styles can, to some extent, also be observed in laboratory and farm animals. Coping styles are characterized by consistent behavioral and neuroendocrine characteristics, some of which seem to be causally linked to each other. Evidence is accumulating that the two coping styles might explain a differential vulnerability to stress mediated disease due to the differential adaptive value of the two coping styles and the accompanying neuroendocrine differentiation.
Keywords: Coping; Aggression; Stress; Disease; Corticosterone
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Rosell, F., & Sanda, J. I. (2006). Potential risks of olfactory signaling: the effect of predators on scent marking by beavers. Behav. Ecol., 17(6), 897–904.
Abstract: Mammals scent mark their territories to advertise occupancy and ownership. However, signaling with scent for territorial defense can have a negative effect by advertising an individual's presence and location to predators. In this study, we measured responses to a simulated territorial intrusion by conspecific adult male Eurasian beavers (Castor fiber) either in the localized presence or in the absence of odor of a predator to test the hypothesis that the territorial defense of free-living beavers would be disrupted by the presence of predation risk in their natural environment. We predicted that beavers would significantly reduce their willingness to countermark intruder's scent in the presence of the scent of predators (wolf [Canis lupus] and lynx [Lynx lynx]), compared with a control (no odor), as responses are in general stronger to predator scent marks than nonpredator scent. Therefore, we also predicted that the effects of nonpredatory mammal scent (neophobic control) (eland [Taurotragus oryx] and horse [Equus cabalus]) are to be expected somewhere in between the effects of the predator odor and a control. Our results suggest that both predator and nonpredator scents reduce beavers response to a simulated intruder's scent mounds and therefore disrupt their territorial defense. However, predator scent had a stronger effect than nonpredator scent. Beavers may therefore be at great risk on territories with predators present because of the trade-off between predator avoidance and territorial defense. Our study demonstrates the potential of predation risk as a powerful agent of counterselection on olfactory signaling behavior.
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Blokland, A. (1998). Reaction time responding in rats. Neurosci Biobehav Rev, 22(6), 847–864.
Abstract: The use of reaction time has a great tradition in the field of human information processing research. In animal research the use of reaction time test paradigms is mainly limited to two research fields: the role of the striatum in movement initiation; and aging. It was discussed that reaction time responding can be regarded as “single behavior”, this term was used to indicate that only one behavioral category is measured, allowing a better analysis of brain-behavior relationships. Reaction time studies investigating the role of the striatum in motor functions revealed that the initiation of a behavioral response is dependent on the interaction of different neurotransmitters (viz. dopamine, glutamate, GABA). Studies in which lesions were made in different brain structures suggested that motor initiation is dependent on defined brain structures (e.g. medialldorsal striatum, prefrontal cortex). It was concluded that the use of reaction time measures can indeed be a powerful tool in studying brain-behavior relationships. However, there are some methodological constraints with respect to the assessment of reaction time in rats, as was tried to exemplify by the experiments described in the present paper. On the one hand one should try to control for behavioral characteristics of rats that may affect the validity of the parameter reaction time. On the other hand, the mean value of reaction time should be in the range of what has been reported in man. Although these criteria were not always met in several studies, it was concluded that reaction time can be validly assessed in rats. Finally, it was discussed that the use of reaction time may go beyond studies that investigate the role of the basal ganglia in motor output. Since response latency is a direct measure of information processing this parameter may provide insight into basic elements of cognition. Based on the significance of reaction times in human studies the use of this dependent variable in rats may provide a fruitful approach in studying brain-behavior relationships in cognitive functions.
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Custance DM, Whiten A, & Bard KA. (1995). Can young chimpanzees imitate arbitrary actions? Hayes and Hayes (1952) revisited. Behavior, 132, 839.
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Vahl, W. K., Lok, T., van der Meer, J., Piersma, T., & Weissing, F. J. (2005). Spatial clumping of food and social dominance affect interference competition among ruddy turnstones. Behav. Ecol., 16(5), 834–844.
Abstract: In studying the success of foraging animals, studies of interference competition have put emphasis on effects of competitor density, whereas studies of resource defense have focused on the effects of the spatial distribution of food within patches. Very few studies have looked at both factors simultaneously, that is, determined whether the effects of competitor density on foraging success depend on the spatial distribution of food. We studied the behavior and the foraging success of ruddy turnstones (Arenaria interpres) using an experiment in which we varied both the presence of a competitor and the food distribution. Because turnstones may differ strongly in their relative dominance status, we also experimentally varied the foragers' relative dominance status. We found that the presence of a competitor only reduced the foraging success of subordinate birds foraging at the clumped food distribution. At this condition, dominant and subordinate birds differed markedly in their foraging success. Contrary to our expectations, we did not observe more agonistic behavior at the clumped food distribution. This indicates that the amount of agonistic behavior observed may be a bad indicator of interference effects. These findings have specific implications for models of interference competition. Most notably they show that the effects of competitor density on agonistic behavior and foraging success may well depend on the spatial distribution of food and the foragers' relative dominance status. Additionally, our results suggest that social dominance will not be fully understood without considering long-term processes such as the formation and maintenance of social dominance hierarchies.
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