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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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Silk, J., Cheney, D., & Seyfarth, R. (2013). A practical guide to the study of social relationships. Evol. Anthropol., 22(5), 213–225.
Abstract: Behavioral ecologists have devoted considerable effort to identifying the sources of variation in individual reproductive success. Much of this work has focused on the characteristics of individuals, such as their sex and rank. However, many animals live in stable social groups and the fitness of individuals depends at least in part on the outcome of their interactions with other group members. For example, in many primate species, high dominance rank enhances access to resources and reproductive success. The ability to acquire and maintain high rank often depends on the availability and effectiveness of coalitionary support. Allies may be cultivated and coalitions may be reinforced by affiliative interactions such as grooming, food sharing, and tolerance. These findings suggest that if we want to understand the selective pressures that shape the social behavior of primates, it will be profitable to broaden our focus from the characteristics of individuals to the properties of the relationships that they form with others. The goal of this paper is to discuss a set of methods that can be used to quantify the properties of social relationships.
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Choleris, E., & Kavaliers, M. (1999). Social Learning in Animals: Sex Differences and Neurobiological Analysis. Pharmacol. Biochem. Behav., 64(4), 767–776.
Abstract: Social learning where an “individual's behavior is influenced by observation of, or interaction with, another animal or its products” has been extensively documented in a broad variety of species, including humans. Social learning occurs within the complex framework of an animal's social interactions that are markedly affected by factors such as dominance hierarchies, family bonds, age, and sex of the interacting individuals. Moreover, it is clear that social learning is influenced not only by important sexually dimorphic social constraints but also that it involves attention, motivational, and perceptual mechanisms, all of which exhibit substantial male-female differences. Although sex differences have been demonstrated in a wide range of cognitive and behavioral processes, investigations of male-female differences in social learning and its neurobiological substrates have been largely neglected. As such, sex differences in social learning and its neurobiological substrates merit increased attention. This review briefly considers various aspects of the study of social learning in mammals, and indicates where male-female differences have either been described, neglected and, or could have a potential impact. It also describes the results of neurobiological investigations of social learning and considers the relevance of these findings to other sexually dimorphic cognitive processes.
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Cantlon, J. F., & Brannon, E. M. (2007). How Much Does Number Matter to a Monkey (Macaca mulatta)? Journal of Experimental Psychology: Animal Behavior Processes, 33(1), 32–41.
Abstract: Although many animal species can represent numerical values, little is known about how salient number is relative to other object properties for nonhuman animals. In one hypothesis, researchers propose that animals represent number only as a last resort, when no other properties differentiate stimuli. An alternative hypothesis is that animals automatically, spontaneously, and routinely represent the numerical attributes of their environments. The authors compared the influence of number versus that of shape, color, and surface area on rhesus monkeys' (Macaca mulatta) decisions by testing them on a matching task with more than one correct answer: a numerical match and a nonnumerical (color, surface area, or shape) match. The authors also tested whether previous laboratory experience with numerical discrimination influenced a monkey's propensity to represent number. Contrary to the last-resort hypothesis, all monkeys based their decisions on numerical value when the numerical ratio was favorable.
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Krama, T. [1], & Krams, I. [2]. (2005). Cost of mobbing call to breeding pied flycatcher, Ficedula hypoleuca. Behav. Ecol., 16, 37–40.
Abstract: Mobbing signals advertise the location of a stalking predator to all prey in an area and recruit them into the inspection aggregation. Such behavior usually causes the predator to move to another area. However, mobbing calls could be eavesdropped by other predators. Because the predation cost of mobbing calls is poorly known, we investigated whether the vocalizations of the mobbing pied flycatcher, Ficedula hypoleuca, a small hole nesting passerine, increase the risk of nest predation. We used mobbing calls of pied flycatchers to examine if they could lure predators such as the marten, Martes martes. This predator usually hunts by night and may locate its mobbing prey while resting nearby during the day. Within each of 56 experimental plots, from the top of one nest-box we played back mobbing sounds of pied flycatchers, whereas blank tapes were played from the top of another nest-box. The trials with mobbing calls were carried out before sunset. We put pieces of recently abandoned nests of pied flycatchers and a quail, Coturnix coturnix, egg into each of the nest-boxes. Nest-boxes with playbacks of mobbing calls were depredated by martens significantly more than were nest-boxes with blank tapes. The results of the present study indicate that repeated conspicuous mobbing calls may carry a significant cost for birds during the breeding season.
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Graf, P., König von Borstel, U., & Gauly, M. (2014). Practical considerations regarding the implementation of a temperament test into horse performance tests: Results of a large-scale test run. Journal of Veterinary Behavior: Clinical Applications and Research, 9(6), 329–340.
Abstract: Abstract Considering the ever-growing demand of various breeding organizations for an objective, inexpensive, reliable, and easily conducted assessment of the behavior of horses, the aim of our study was to implement a novel-object test and a startling test into any kind of breeding performance testing to assess horses' temperament. Additionally, the influence of testing areas (familiar or unfamiliar), riders, and horse factors such as levels of training, breed, and age were of interest. Furthermore, recommendations for the practical implementation concerning the parameters should be given. Therefore, 1,028 horses over a period of 3 years participated in a temperament test consisting of 5 different stimuli. The horses were either ridden (61.8 %) or led by hand (38.2 %) by an unfamiliar professional rider (N = 43) or a familiar rider (N = 20). Live behavioral observations were taken by a trained observer. Overall, horses' scores for reactivity in the present temperament test were distributed over the whole scale, with lower means and higher standard deviations (6.7 ± 2.2-7.6 ± 2.1) than corresponding scores from the conventional personality evaluation in performance tests (7.7 ± 0.8-8.2 ± 0.5; P < 0.01). High correlations (r = 0.3-0.9; P < 0.001) between the scores for reactivity and the other behavioral parameters (emotional expression, activity, time to calm down, rider's aids) show a large influence of these parameters in assessing the horses' temperament. Factors like breed type, sex, and age had significant influences (P < 0.001) on different scores of the temperament test. In most cases, the rider or handler had no influence on the different scores assessed during the temperament test. The training level and the testing modus never had a significant influence on different scores. Only the testing station or location had a small influence on the scores for the stimulus “bridge” in some horses. Based on the results, it could be concluded that an implementation of a temperament tests into performance testing is possible during various types of testing procedure. Especially the assessment of reactivity, emotional expression, interest in the stimulus and rider's aids during and after passing the stimulus, as well as the time to calm down are important parameters for analyzing the horses' personality.
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Berger, A. (2015). Evaluation of living conditions in free running animals by chronobiological analysis of continuously recorded behavioural data. In Proceedings of the 3. International Equine Science Meeting.
Abstract: We developed a biorhythmical method to assess behaviour patterns and to evaluate living conditions of animals. All kinds of continuous and equidistant long-term recordings of behaviour are suitable for this method. As simple behavioural parameters, such as motor activity, can be conveniently recorded by telemetry from wild animals now, it is possible to investigate stressors by analysing its biorhythmic structure. It is the purpose of this report to describe the basic idea, and the procedure, and to give some examples of application measured on Przewalski horses in an Semireserve.
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Giles J.K et al. (1963). Methods of Training Horses.
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Branson, N. J., & Rogers, L. J. (2006). Relationship between paw preference strength and noise phobia in Canis familiaris. J. Comp. Psychol., 120(3), 176–183.
Abstract: The authors investigated the relationship between degree of lateralization and noise phobia in 48 domestic dogs (Canis familiaris) by scoring paw preference to hold a food object and relating it to reactivity to the sounds of thunderstorms and fireworks, measured by playback and a questionnaire. The dogs without a significant paw preference were significantly more reactive to the sounds than the dogs with either a left-paw or right-paw preference. Intense reactivity, therefore, is associated with a weaker strength of cerebral lateralization. The authors note the similarity between their finding and the weaker hand preferences shown in humans suffering extreme levels of anxiety and suggest neural mechanisms that may be involved. (PsycINFO Database Record (c) 2010 APA, all rights reserved)
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Berger, J., & Cunningham, C. (1988). Size-Related Effects on Search Times in North American Grassland Female Ungulates. Ecology, 69(1), 177–183.
Abstract: Feeding and searching (= vigilance) rates arise as a result of many interrelated factors including trophic level, diet, reproductive condition, sex, habitat, body mass, and potential predation pressure. Because of unique ecological conditions in which the confounding influences of all but two of these variables could be minimized, we examined the hypothesis that body mass alone accounts for interspecific differences in search times, and tested it with females of four sympatric native North American ungulates (Bison bison, Antilocapra americana, Ovis canadensis, and Odocoileus hemionus). When the effects of group size were controlled, smaller bodied species were more vigilant (per unit body mass) than larger ones. However, search times (ST) also scaled to body mass, and between 81 and 97% of the ST variance was explained by either exponential or power functions. To remove the potential bias that predators exert different influences on species of varying size, search times of bison in areas with and without their major predator, wolves (Canis lupus), were contrasted; search times did not differ between sites. Our results highlight the importance of designing field research that controls for confounding variables prior to attempting to scale behavioral processes to ecological events. See full-text article at JSTOR
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