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Lusseau, D., & Conradt, L. (2009). The emergence of unshared consensus decisions in bottlenose dolphins. Behav. Ecol. Sociobiol., 63(7), 1067–1077.
Abstract: Abstract Unshared consensus decision-making processes, in which one or a small number of individuals make the decision for the rest of a group, are rarely documented. However, this mechanism can be beneficial for all group members when one individual has greater knowledge about the benefits of the decision than other group members. Such decisions are reached during certain activity shifts within the population of bottlenose dolphins residing in Doubtful Sound, New Zealand. Behavioral signals are performed by one individual and seem to precipitate shifts in the behavior of the entire group: males perform side flops and initiate traveling bouts while females perform upside-down lobtails and terminate traveling bouts. However, these signals are not observed at all activity shifts. We find that, while side flops were performed by males that have greater knowledge than other male group members, this was not the case for females performing upside-down lobtails. The reason for this could have been that a generally high knowledge about the optimal timing of travel terminations rendered it less important which individual female made the decision.
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Matsumura, S., & Kobayashi, T. (1998). A game model for dominance relations among group-living animals. Behav. Ecol. Sociobiol., 42(2), 77–84.
Abstract: Abstract We present here an attempt to understand behaviors of dominant individuals and of subordinate individuals as behavior strategies in an asymmetric “hawk-dove” game. We assume that contestants have perfect information about relative fighting ability and the value of the resource. Any type of asymmetry, both relevant to and irrelevant to the fighting ability, can be considered. It is concluded that evolutionarily stable strategies (ESSs) depend on the resource value (V), the cost of injury (D), and the probability that the individual in one role will win (x). Different ESSs can exist even when values of V, D, and x are the same. The characteristics of dominance relations detected by observers may result from the ESSs that the individuals are adopting. The model explains some characteristics of dominance relations, for example, the consistent outcome of contests, the rare occurrence of escalated fights, and the discrepancy between resource holding potential (RHP) and dominance relations, from the viewpoint of individual selection.
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Purvis, A. (2006). The h index: playing the numbers game. Trends. Ecol. Evol, 21(8), 422.
Abstract: Article Outline
References
The ‘h index’ was developed recently as a measure of research performance [1]: a researcher's h is the number of his or her papers that have been cited at least h times. In their thoughtful critique of the index, Kelly and Jennions [2] point out many ways in which h is no better than ‘traditional’ bibliometrics, such as total citation counts. However, there is one way in which, for researchers, it could be very much better, especially if (as Hirsch suggests [1]) it is to inform hiring and promotion decisions. The skewed nature of the distribution of citations among publications means that most researchers have several papers that nearly but not quite count. Consequently, h can be distorted much more easily than can total citation count just by finding a subtle way to cite one's own papers that are ‘bubbling under’. Incidentally, bats show broadly the same life-history allometries as other mammalian clades [3].
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Whitehead, H. (2009). SOCPROG programs: analysing animal social structures. Behav. Ecol. Sociobiol., 63(5), 765–778.
Abstract: Abstract SOCPROG is a set of programs which analyses data on animal associations. Data usually come from observations of the social behaviour of individually identifiable animals. Associations among animals, sampling periods, restrictions on the data and association indices can be defined very flexibly. SOCPROG can analyse data sets including 1,000 or more individuals. Association matrices are displayed using sociograms, principal coordinates analysis, multidimensional scaling and cluster analyses. Permutation tests, Mantel and related tests and matrix correlation methods examine hypotheses about preferred associations among individuals and classes of individual. Weighted network statistics are calculated and can be tested against null hypotheses. Temporal analyses include displays of lagged association rates (rates of reassociation following an association). Models can be fitted to lagged association rates. Multiple association measures, including measures produced by other programs such as genetic or range use data, may be analysed using Mantel tests and principal components analysis. SOCPROG also performs mark-recapture population analyses and movement analyses. SOCPROG is written in the programming language MATLAB and may be downloaded free from the World Wide Web.
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Noë, R., & Hammerstein, P. (1995). Biological markets. Trends. Ecol. Evol, 10(8), 336–339.
Abstract: In biological markets, two classes of traders exchange commodities to their mutual benefit. Characteristics of markets are: competition within trader classes by contest or outbidding; preference for partners offering the highest value; and conflicts over the exchange value of commodities. Biological markets are currently studied under at least three different headings: sexual selection, intraspecific cooperation and interspecific mutualism. The time is ripe for the development of game theoretic models that describe the common core of biological markets and integrate existing knowledge from the separate fields.
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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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Conradt, L., & Roper, T. J. (2005). Consensus decision making in animals. Trends Ecol Evol, 20(8), 449–456.
Abstract: Individual animals routinely face decisions that are crucial to their fitness. In social species, however, many of these decisions need to be made jointly with other group members because the group will split apart unless a consensus is reached. Here, we review empirical and theoretical studies of consensus decision making, and place them in a coherent framework. In particular, we classify consensus decisions according to the degree to which they involve conflict of interest between group members, and whether they involve either local or global communication; we ask, for different categories of consensus decision, who makes the decision, what are the underlying mechanisms, and what are the functional consequences. We conclude that consensus decision making is common in non-human animals, and that cooperation between group members in the decision-making process is likely to be the norm, even when the decision involves significant conflict of interest.
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Connor, R. C., Mann, J., Tyack, P. L., & Whitehead, H. (1998). Social evolution in toothed whales. Trends. Ecol. Evol, 13(6), 228–232.
Abstract: Two contrasting results emerge from comparisons of the social systems of several odontocetes with terrestrial mammals. Researchers have identified remarkable convergence in prominent features of the social systems of odontocetes such as the sperm whale and bottlenose dolphin with a few well-known terrestrial mammals such as the elephant and chimpanzee. In contrast, studies on killer whales and Baird's beaked whale reveal novel social solutions to aquatic living. The combination of convergent and novel features in odontocete social systems promise a more general understanding of the ecological determinants of social systems in both terrestrial and aquatic habitats, as well as the relationship between relative brain size and social evolution.
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Ferrari, M. C. O., Capitania-Kwok, T., & Chivers, D. P. (2006). The role of learning in the acquisition of threat-sensitive responses to predator odours. Behav. Ecol. Sociobiol., 60(4), 522–527.
Abstract: The supposition that prey animals respond to a predator with an intensity that matches the risk posed by the predator is known as the threat-sensitive predator avoidance hypothesis. Many studies have provided support for this hypothesis; yet, few studies have attempted to determine how such abilities are acquired by prey species. In this study, we investigated whether fathead minnows (Pimephales promelas) could learn to recognize an unknown predator (northern pike, Esox lucius) in such a way that they could match the intensity of their antipredator response with the threat posed by the predator. We exposed pike-naive minnows to conspecific alarm cues paired with either a high or low concentration of pike odor. The following day, both groups were tested for a response to either high or low concentration of pike odor alone. We found that minnows conditioned with alarm cues paired with a given concentration of pike odor subsequently responded with a higher intensity to higher concentrations of pike odor, and with a lower intensity to lower concentrations of pike odor. These results demonstrate that during a single conditioning trial, minnows learn the identity of the predator in a threat-sensitive manner. Minnows use predator odor concentrations that they experience in subsequent interactions to adjust the intensity of their antipredator behavior. © Springer-Verlag 2006.
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Tibbetts, E. A., & Dale, J. (2007). Individual recognition: it is good to be different. Trends. Ecol. Evol, 22(10), 529–537.
Abstract: Individual recognition (IR) behavior has been widely studied, uncovering spectacular recognition abilities across a range of taxa and modalities. Most studies of IR focus on the recognizer (receiver). These studies typically explore whether a species is capable of IR, the cues that are used for recognition and the specializations that receivers use to facilitate recognition. However, relatively little research has explored the other half of the communication equation: the individual being recognized (signaler). Provided there is a benefit to being accurately identified, signalers are expected to actively broadcast their identity with distinctive cues. Considering the prevalence of IR, there are probably widespread benefits associated with distinctiveness. As a result, selection for traits that reveal individual identity might represent an important and underappreciated selective force contributing to the evolution and maintenance of genetic polymorphisms.
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