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Author |
Clegg, H.A.; Buckley, P.; Friend, M.A.; McGreevy, P.D. |
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Title |
The ethological and physiological characteristics of cribbing and weaving horses |
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Journal Article |
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2008 |
Publication |
Applied Animal Behaviour Science |
Abbreviated Journal |
Appl. Anim. Behav. Sci. |
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109 |
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1 |
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68-76 |
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Horse; Stereotypy; Digestion; Gut transit; Stress |
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Data were gathered on the behavioural and physiological characteristics of five cribbers, six weavers and six non-stereotypic (control) mature Thoroughbred geldings for a period of 16 weeks. The horses were hired from their owners and stabled individually throughout the trial. Cribbers and weavers had been known to stereotype for at least 12 months prior to commencement of the study. Behavioural data were collected using video surveillance. Cribbers stereotyped most frequently (PÂ <Â 0.001) in the period 2-8Â h following delivery of concentrated food, reinforcing the suggestion that diet is implicated in cribbing behaviour. Weavers stereotyped most frequently (PÂ <Â 0.001) during periods of high environmental activity such as during routine pre-feeding activities and in the hour prior to daily turnout, presumably when anticipation and stimulation were at their highest levels. Cribbers and weavers took longer than control horses to fully consume their ration, suggesting possible differences in motivation to feed, distress levels, satiety mechanisms or abdominal discomfort. Physiological data were collected throughout the trial and there were no differences in oro-caecal transit time, digestibility, plasma cortisol concentration or heart rate among the three behavioural groups. |
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0168-1591 |
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Equine Behaviour @ team @ |
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4768 |
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Clotfelter, E.D.; Paolino, A.D. |
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Title |
Bystanders to contests between conspecifics are primed for increased aggression in male fighting fish |
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Journal Article |
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Year |
2003 |
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Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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66 |
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2 |
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343-347 |
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We performed two experiments in which we allowed a male fighting fish, Betta splendens, designated a bystander, to observe aggressive contests between pairs of male conspecifics. Another male (naive male) observed an empty tank or two nonaggressive males, depending on the experiment. Immediately after these observation periods, we allowed the bystander and naive male to interact in a neutral area. In both experiments, bystander males were dominant over naive males in a significant number of the encounters. Bystander males performed significantly more aggressive behaviours (displays, chases and bites) than did naive males. Differences in dominance were not due to chance differences in body size. These findings demonstrate that exposure to aggression between conspecifics increases aggressive motivation in bystander male fighting fish. We discuss briefly the implications of such social experience on the formation of dominance hierarchies. Copyright 2003 Published by Elsevier Ltd on behalf of The Association for the Study of Animal Behaviour. |
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refbase @ user @ |
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338 |
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Cloutier, S.; Newberry, R.C. |
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Title |
Differences in skeletal and ornamental traits between laying hen cannibals, victims and bystanders |
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Journal Article |
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Year |
2002 |
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Applied Animal Behaviour Science |
Abbreviated Journal |
Appl. Anim. Behav. Sci. |
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77 |
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2 |
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115-126 |
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Domestic fowl; Asymmetry; Skeletal traits; Comb size; Cannibalism |
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We compared the size of skeletal and ornamental traits, and asymmetries in bilateral skeletal traits, between victims of cannibalism, cannibals and bystanders within small groups of caged female White Leghorns at the time of cannibalistic attacks (i.e. injurious pecks resulting in bleeding). We hypothesised that victims of cannibalism have discernible morphological traits that predispose them to cannibalistic attack. We predicted that victims would have smaller skeletal traits (body length, ulna length, metatarsus length and width, toe length), lower body weight, poorer body condition, smaller combs and more asymmetrical bilateral skeletal traits than their flock mates. Contrary to our prediction, victims of cannibalistic attacks to the head/neck area (N=23) tended to have larger combs than their flock mates (Wilcoxon matched-pairs signed-ranks test, S=59, P=0.037, NS after sequential Bonferroni adjustment). Their cannibals were more asymmetrical than non-cannibalistic bystanders (metatarsus length, S=48, P=0.011 and composite asymmetry, S=62.5, P=0.002, significant after sequential Bonferroni adjustment). In agreement with our prediction, victims of cannibalistic attacks to other body parts (N=27), including the back, wings, rump, tail, cloaca, abdomen and toes, were more asymmetrical (composite asymmetry, S=78, P=0.022, significant after sequential Bonferroni adjustment) and tended to have lower body weights (S=79.5, P=0.029, NS after sequential Bonferroni adjustment) than their flock mates. Their cannibals did not differ in skeletal or ornamental traits from the non-participating bystanders. The results suggest that large combs either elicit attacks to the head and neck area or increase vulnerability to injury during such attacks. Attacks to other body parts appear to be directed towards birds with signs of weakness relative to their flock mates. In these attacks, there were no distinguishing features separating cannibals from bystanders, suggesting that the bystanders could all be potential cannibals. |
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2092 |
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Author |
Cloutier, S.; Newberry, R.C.; Honda, K. |
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Title |
Comparison of social ranks based on worm-running and aggressive behaviour in young domestic fowl |
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Journal Article |
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2004 |
Publication |
Behavioural Processes |
Abbreviated Journal |
Behav. Process. |
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65 |
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1 |
Pages |
79-86 |
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Aggression; Social behaviour; Dominance; Play; Chickens; Animal welfare |
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Worm-running is behaviour in which a chick runs carrying a worm-like object while flock mates follow and attempt to grab the object from its beak. We hypothesised that social ranks based on worm-running frequency are stable over time and are positively correlated with social ranks based on success in aggressive interactions when older. At 8-12 days of age, we scored worm-running in 17 groups of 12 female White Leghorn chicks during three 10-min tests. Based on instantaneous scans at 5-s intervals, the bird carrying the `worm' most often was placed in rank one and so on down the rank order. These tests were repeated at 68-70 days of age. An aggression index for each bird was calculated as the number of aggressive acts given, divided by the number given and received, during three 1-h observation periods when the birds were 68-70 days. Ranks obtained in worm-running tests were positively correlated over the two age periods (P<0.05) but were not correlated with ranks based on the aggression index (P>0.05). Our results indicate that worm-running ranks are not predictive of success in aggressive interactions. Instead, worm-running fits some criteria for play. |
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2090 |
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Author |
Cloutier, S.; Newberry, R.C.; Honda, K.; Alldredge, J.R. |
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Title |
Cannibalistic behaviour spread by social learning |
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Journal Article |
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Year |
2002 |
Publication |
Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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63 |
Issue |
6 |
Pages |
1153-1162 |
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We hypothesized that social learning is involved in the spread of cannibalism in domestic fowlGallus gallus domesticus . To investigate this hypothesis without harming birds, we used an inanimate chicken model as our cannibalism stimulus. We randomly assigned flocks of 12 White Leghorn pullets to one of two treatments: (1) flocks with two trained demonstrators (N=9) and (2) control flocks (N=8). Demonstrators were trained to pierce a membrane covering a dish of chicken blood and consume the blood. To assess the effect of access to the cannibalism stimulus during demonstrations, we randomly assigned observer pairs to one of two observer treatments: (1) observe stimulus through a wire mesh partition and (2) observe stimulus within the same enclosure. We conducted five 10-min demonstration sessions, each followed by a 10-min test of each observer pair in the absence of demonstrators, over a period of 15 days when the birds were 41-55 days of age, and two further tests at 63-64 and 91-92 days of age. Pairs that observed demonstrators piercing a membrane and consuming blood were more likely to perform this task when tested than control pairs. Learning of the task was enhanced by direct access to the cannibalism stimulus rather than observing it through a wire mesh partition. Blood consumption during tests was increased by direct access to the cannibalism stimulus during demonstration sessions. The birds made bigger holes in the membrane when tested after observing trained demonstrators and after having direct access to the stimulus. Our results provide the first experimental evidence that social learning can contribute to the spread of cannibalistic behaviour in domestic fowl. We suggest that stimulus enhancement and observational conditioning were the social-learning mechanisms involved. Copyright 2002 The Association for the Study of Animal Behaviour. Published by Elsevier Science Ltd. All rights reserved. |
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2091 |
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Clutton-Brock, J. |
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Title |
Origins of the dog: domestication and early history |
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1995 |
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The Domestic Dog: Its Evolution, Behaviour and Interactions with People |
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Cambridge University Press |
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Cambridge |
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Serpell, J.A. |
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Equine Behaviour @ team @ Clutton-Brock1995 |
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6247 |
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Clutton-Brock, T.H.; Albon, S.D.; Gibson, R.M.; Guinness, F.E. |
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Title |
The logical stag: Adaptive aspects of fighting in red deer (Cervus elaphus L.) |
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1979 |
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Animal Behaviour. |
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Anim. Behav. |
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27 |
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Part 1 |
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211-225 |
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For red deer stags, fighting both has appreciable costs and yields considerable benefits. Up to 6% of rutting stags are permanently injured each year, while fighting success and reproductive success are closely related, within age groups as well as across them. Fighting behaviour is sensitive to changes in the potential benefits of fighting: stags fight most frequently and most intensely where potential benefits are high and tend to avoid fighting with individuals they are unlikely to beat. The relevance of these findings to theoretical models of fighting behaviour is discussed. |
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860 |
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Clutton-Brock, T.H.; Parker, G.A. |
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Title |
Sexual coercion in animal societies |
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1995 |
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Animal Behaviour. |
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Anim. Behav. |
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49 |
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5 |
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1345-1365 |
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In a wide range of animal species, males coerce females to mate with them, either by physically forcing them to mate, by harassing them until they mate or by punishing persistent refusal to mate. The first section of this paper argues that the possibility of forced copulation can generate arms races between males and females that may have substantial costs to both sexes. In the second section, it is suggested that sexual harassment commonly represents a `war of attrition' between the sexes; existing game theory models that may apply to sexual conflict over mating decisions are reviewed. The third section develops a simple prospective model for the evolution of intimidation by punishment in situations where males can raise the probability that females will accept their advances in future by punishing them for refusal to mate. Where the benefits of sexual coercion to males are high, all three male strategies may develop to a point where they have substantial costs to females. In the final section, evidence that female behaviour is adapted to minimizing these costs is reviewed. |
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757 |
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Coleman, K.; Wilson, D.S. |
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Title |
Shyness and boldness in pumpkinseed sunfish: individual differences are context-specific |
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1998 |
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Animal Behaviour. |
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Anim. Behav. |
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56 |
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4 |
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927-936 |
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Natural selection often promotes a mix of behavioural phenotypes in a population. Adaptive variation in the propensity to take risks might explain individual differences in shyness and boldness in humans and other species. It is often implicitly assumed that shyness and boldness are general personality traits expressed across many situations. From the evolutionary standpoint, however, individual differences that are adaptive in one context (e.g. predator defence) may not be adaptive in other contexts (e.g. exploration of the physical environment or intraspecific social interactions). We measured the context specificity of shyness and boldness in a natural population of juvenile pumpkinseed sunfish,Lepomis gibbosus, by exposing the fish to a potentially threatening stimulus (a red-tipped metrestick extended towards the individual) and a nonthreatening stimulus (a novel food source). We also related these measures of shyness and boldness to behaviours observed during focal observations, both before and after the introduction of a predator (largemouth bass,Micropterus salmoides). Consistent individual differences were found within both contexts, but individual differences did not correlate across contexts. Furthermore, fish that were scored as intermediate in their response to the metrestick behaved most boldly as foragers and in response to the bass predators. These results suggest that shyness and boldness are context-specific and may not exist as a one-dimensional behavioural continuum even within a single context. |
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Conradt, L.; Roper, T.J. |
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Title |
Deciding group movements: Where and when to go |
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2010 |
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Behavioural Processes |
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Behav. Process. |
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84 |
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3 |
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675-677 |
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activity synchronisation; aggregation rules; collective decisions; democracy; group decisions; sexual segregation; decision sharing; social choice theory |
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A group of animals can only move cohesively, if group members “somehow” reach a consensus about the timing (e.g., start) and the spatial direction/destination of the collective movement. Timing and spatial decisions usually differ with respect to the continuity of their cost/benefit distribution in such a way that, in principle, compromises are much more feasible in timing decision (e.g. median preferred time) than they are in spatial decisions. The consequence is that consensus costs connected to collective timing decisions are usually less skewed amongst group members than are consensus costs connected to spatial decisions. This, in turn, influences the evolution of decision sharing: sharing in timing decisions is most likely to evolve when conflicts are high relative to group cohesion benefits, while sharing in spatial decisions is most likely to evolve in the opposite situation. We discuss the implications of these differences for the study of collective movement decisions. |
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Equine Behaviour @ team @ |
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5086 |
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