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Andrew, R.J. |
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Title |
Changes in visual responsiveness following intercollicular lesions and their effects on avoidance and attack |
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1974 |
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Brain, Behavior and Evolution |
Abbreviated Journal |
Brain Behav Evol |
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10 |
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4-5 |
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400-424 |
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Animals; Chickens; Humans; Male; Mutism; Superior Colliculi/*physiology; Tectum Mesencephali; Testosterone; Visual Fields; Vocalization, Animal |
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In the normal chick, conspicuous visual stimuli induce targetting and pecking together, with vocalization. All three are abolished by lesion of the intercollicular area (ICo) or of connections passing through its medial margin. After such lesions, chicks also cease to treat significant visual stimuli as if they were startling and exciting, and may delay response as a result. However, they are still able to recognise, orient accurately to, and respond appropriately to, a variety of complex visual stimuli (e.g. food grains, copulation object). In addition, they are little affected by strange surroundings. Lesion evidence suggests the mammalian subcollicular area to have similar functions to the ICo and to be homologous with it. A route (present in bird), which is well-known in mammals for its association with threat, defense and escape evoked by strange and frightening objects (amygdala-diencephalic periventricular system-central mesencephalic grey, A-DPS-CMG) is stimuli via the 2 ICo (subcollicular area). Two different mechanisms may be involved caudal to the ICo. One consists of tectal afferents which might modulate the evocation of targetting, pecking and other responses via the tectum. The other is the predorsal system of tectal efferents which may mediate such responses. Classical syndromes of tameness and unresponsiveness produced by various interruptions of the A-DPS-CMG route may depend on interruption of connections to these midbrain mechanisms. Attack is depressed by ICo lesions as one aspect of reduced responsiveness to conspicuous and startling visual stimuli. Avoidance, which is apparently mediated by a separate system, much as in Anura, is facilitated. |
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0006-8977 |
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PMID:1169102 |
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Equine Behaviour @ team @ |
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4626 |
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Lefebvre, L.; Reader, S.M.; Sol, D. |
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Brains, Innovations and Evolution in Birds and Primates |
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2004 |
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Brain, Behavior and Evolution |
Abbreviated Journal |
Brain. Behav. Evol. |
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63 |
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4 |
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233-246 |
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Innovation W Brain evolution W Hyperstriatum ventrale W Neostriatum W Isocortex W Birds W Primates W Tool use W Invasion biology |
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Abstract
Several comparative research programs have focusedon the cognitive, life history and ecological traits thataccount for variation in brain size. We review one ofthese programs, a program that uses the reported frequencyof behavioral innovation as an operational measureof cognition. In both birds and primates, innovationrate is positively correlated with the relative size of associationareas in the brain, the hyperstriatum ventrale andneostriatum in birds and the isocortex and striatum inprimates. Innovation rate is also positively correlatedwith the taxonomic distribution of tool use, as well asinterspecific differences in learning. Some features ofcognition have thus evolved in a remarkably similar wayin primates and at least six phyletically-independent avianlineages. In birds, innovation rate is associated withthe ability of species to deal with seasonal changes in theenvironment and to establish themselves in new regions,and it also appears to be related to the rate atwhich lineages diversify. Innovation rate provides a usefultool to quantify inter-taxon differences in cognitionand to test classic hypotheses regarding the evolution ofthe brain. |
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Equine Behaviour @ team @ |
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4738 |
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Pérez-Barbería, F.J.; Shultz, S.; Dunbar, R.I.M.; Janis, C. |
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Title |
Evidence For Coevolution Of Sociality And Relative Brain Size In Three Orders Of Mammals |
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2007 |
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Evolution |
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61 |
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12 |
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2811-2821 |
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Brain size, carnivores, coevolution, primates, sociality, ungulates |
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Abstract
As the brain is responsible for managing an individual's behavioral response to its environment, we should expect that large relative brain size is an evolutionary response to cognitively challenging behaviors. The “social brain hypothesis†argues that maintaining group cohesion is cognitively demanding as individuals living in groups need to be able to resolve conflicts that impact on their ability to meet resource requirements. If sociality does impose cognitive demands, we expect changes in relative brain size and sociality to be coupled over evolutionary time. In this study, we analyze data on sociality and relative brain size for 206 species of ungulates, carnivores, and primates and provide, for the first time, evidence that changes in sociality and relative brain size are closely correlated over evolutionary time for all three mammalian orders. This suggests a process of coevolution and provides support for the social brain theory. However, differences between taxonomic orders in the stability of the transition between small-brained/nonsocial and large-brained/social imply that, although sociality is cognitively demanding, sociality and relative brain size can become decoupled in some cases. Carnivores seem to have been especially prone to this. |
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doi: 10.1111/j.1558-5646.2007.00229.x |
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Equine Behaviour @ team @ |
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4781 |
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Connor, R.C.; Mann, J.; Tyack, P.L.; Whitehead, H. |
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Title |
Social evolution in toothed whales |
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Journal Article |
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Year |
1998 |
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Trends in Ecology & Evolution |
Abbreviated Journal |
Trends. Ecol. Evol |
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13 |
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6 |
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228-232 |
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odontocetes; toothed whales; social evolution; communication; bottlenose dolphins; sperm whales; long-term studies; foraging |
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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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0169-5347 |
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Equine Behaviour @ team @ |
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4789 |
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Conradt, L.; Roper, T.J. |
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Consensus decision making in animals |
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Journal Article |
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Year |
2005 |
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Trends in Ecology & Evolution (Personal Edition) |
Abbreviated Journal |
Trends Ecol Evol |
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20 |
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8 |
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449-456 |
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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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Department of Biology and Environmental Science, John Maynard Smith Building, University of Sussex, Brighton, UK, BN1 9QG. L.Conradt@sussex.ac.uk |
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0169-5347 |
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PMID:16701416 |
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Equine Behaviour @ team @ |
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4802 |
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Herbert Gintis; Samuel Bowles; Robert Boyd; Ernst Fehr |
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Explaining altruistic behavior in humans |
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Journal Article |
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2003 |
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Evolution and Human Behaviour |
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24 |
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3 |
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153-172 |
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Altruism; Reciprocity; Experimental games; Evolution of cooperation |
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Recent experimental research has revealed forms of human behavior involving interaction among unrelated individuals that have proven difficult to explain in terms of kin or reciprocal altruism. One such trait, strong reciprocity is a predisposition to cooperate with others and to punish those who violate the norms of cooperation, at personal cost, even when it is implausible to expect that these costs will be repaid. We present evidence supporting strong reciprocity as a schema for predicting and understanding altruism in humans. We show that under conditions plausibly characteristic of the early stages of human evolution, a small number of strong reciprocators could invade a population of self-regarding types, and strong reciprocity is an evolutionary stable strategy. Although most of the evidence we report is based on behavioral experiments, the same behaviors are regularly described in everyday life, for example, in wage setting by firms, tax compliance, and cooperation in the protection of local environmental public goods. |
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1090-5138 |
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Equine Behaviour @ team @ S1090-5138(02)00157-5 |
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4943 |
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Noë, R.; Hammerstein, P. |
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Biological markets |
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Journal Article |
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1995 |
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Trends in Ecology & Evolution |
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Trends. Ecol. Evol |
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10 |
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8 |
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336-339 |
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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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Equine Behaviour @ team @ |
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4993 |
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Ishida, N.; Oyunsuren, T.; Mashima, S.; Mukoyama, H.; Saitou, N. |
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Mitochondrial DNA sequences of various species of the genus Equus with special reference to the phylogenetic relationship between Przewalskii's wild horse and domestic horse |
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1995 |
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Journal of Molecular Evolution |
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J Mol Evol |
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41 |
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2 |
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180-188 |
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Animals; Base Sequence; Chromosomes; Conserved Sequence/genetics; DNA, Mitochondrial/*genetics; Evolution; Genetic Variation/*genetics; Horses/*genetics; Molecular Sequence Data; *Phylogeny; RNA, Transfer, Pro/genetics; Sequence Alignment; Sequence Analysis, DNA |
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The noncoding region between tRNAPro and the large conserved sequence block is the most variable region in the mammalian mitochondrial DNA D-loop region. This variable region (ca. 270 bp) of four species of Equus, including Mongolian and Japanese native domestic horses as well as Przewalskii's (or Mongolian) wild horse, were sequenced. These data were compared with our recently published Thoroughbred horse mitochondrial DNA sequences. The evolutionary rate of this region among the four species of Equus was estimated to be 2-4 x 10(-8) per site per year. Phylogenetic trees of Equus species demonstrate that Przewalskii's wild horse is within the genetic variation among the domestic horse. This suggests that the chromosome number change (probably increase) of the Przewalskii's wild horse occurred rather recently. |
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Laboratory of Molecular and Cellular Biology, Japan Racing Association, Tokyo |
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0022-2844 |
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PMID:7666447 |
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Equine Behaviour @ team @ |
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5042 |
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Purvis, A. |
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The h index: playing the numbers game |
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2006 |
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Trends in Ecology & Evolution |
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Trends. Ecol. Evol |
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21 |
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8 |
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422-422 |
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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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0169-5347 |
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Equine Behaviour @ team @ |
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5046 |
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Rands, S.A.; Cowlishaw, G.; Pettifor, R.A.; Rowcliffe, J.M.; Johnstone, R.A. |
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The emergence of leaders and followers in foraging pairs when the qualities of individuals differ |
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2008 |
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BMC Evolutionary Biology |
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BMC Evol Biol |
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8 |
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51 |
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Animals; *Feeding Behavior; *Food Chain; *Models, Biological; *Social Dominance |
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BACKGROUND: Foraging in groups offers animals a number of advantages, such as increasing their likelihood of finding food or detecting and avoiding predators. In order for a group to remain together, there has to be some degree of coordination of behaviour and movement between its members (which may in some cases be initiated by a decision-making leader, and in other cases may emerge as an underlying property of the group). For example, behavioural synchronisation is a phenomenon where animals within a group initiate and then continue to conduct identical behaviours, and has been characterised for a wide range of species. We examine how a pair of animals should behave using a state-dependent approach, and ask what conditions are likely to lead to behavioural synchronisation occurring, and whether one of the individuals is more likely to act as a leader. RESULTS: The model we describe considers how the energetic gain, metabolic requirements and predation risks faced by the individuals affect measures of their energetic state and behaviour (such as the degree of behavioural synchronisation seen within the pair, and the value to an individual of knowing the energetic state of its colleague). We explore how predictable changes in these measures are in response to changes in physiological requirements and predation risk. We also consider how these measures should change when the members of the pair are not identical in their metabolic requirements or their susceptibility to predation. We find that many of the changes seen in these measures are complex, especially when asymmetries exist between the members of the pair. CONCLUSION: Analyses are presented that demonstrate that, although these general patterns are robust, care needs to be taken when considering the effects of individual differences, as the relationship between individual differences and the resulting qualitative changes in behaviour may be complex. We discuss how these results are related to experimental observations, and how the model and its predictions could be extended. |
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Department of Zoology, University of Cambridge, Downing Street, Cambridge CB2 3EJ, UK. sean.rands@bristol.ac.uk |
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1471-2148 |
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PMID:18282297 |
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Equine Behaviour @ team @ |
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5126 |
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