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R. A. J. Taylor |
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The Behavioural Basis of Redistribution I. The Delta -Model Concept |
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1981 |
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The Journal of Animal Ecology |
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T. J. Anim. Ecol. |
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50 |
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2 |
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573-586 |
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(1) A conceptual model is developed in which spatial behaviour is density-dependent. The behaviour is classified as congregatory or migratory according to whether it results in movement towards or away from population concentrations. (2) Spatial behaviour is shown to result from both individual and population interactions. (3) The stability properties of the model are explored and it is shown how, under particular conditions, populations obeying the model have a population density regulating mechanism. (4) The similarity between the model and the potential energy curve of physics is noted, but it is emphasized that this is a behavioural not a physical model. |
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refbase @ user @ |
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720 |
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Garott, R.A. |
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Title |
Sex Ratios and Differential Survival of Feral Hors |
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1991 |
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Journal of Animal Ecology |
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J Anim Ecol |
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60 |
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3 |
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929-936 |
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(1) Sex and age data were collected on 60 111 feral horses (Equus caballus L.) removed from eighty-nine areas in Nevada, Wyoming, and Oregon between 1976 and 1987. (2) Sex ratios of young seldom differed from parity; however, sex ratios of adults were commonly skewed toward females. No evidence of differential capture probability between adult males and females could be detected; therefore, skewed adult sex ratios were attributed to differential survival. (3) Age-specific trends in sex ratios indicated that the proportion of males steadily decreased from near parity in foals, to lows of 0.61-0.77 in the 4-5-year age-classes. The trend then reversed with males becoming predominant (1.08-1.36) in the > 10 years age-class. (4) Population simulations suggest that survival diffentials of 0.05-0.07, favouring females to 4 years of age, and 0.02-0.04 favouring males in older age-classes were required to mimic observed age-specific sex ratio changes. To obtain the high proportion of males in the > 10-years age-class, onset of senescence also had to be earlier for females. (5) Causes for differential survival in the immature age-classes are uncertain, but may relate to behavioural or metabolic differences between the sexes. Differential survival between adult males and females is attributed to differences in the energetic costs of reproduction and disparity in their reproductive life spans. |
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Equine Behaviour @ team @ |
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2294 |
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Mason, W.A.; Hollis, J.H. |
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Title |
Communication between young rhesus monkeys |
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Journal Article |
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1962 |
Publication |
Animal Behaviour. |
Abbreviated Journal |
Anim. Behav. |
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10 |
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3-4 |
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211-221 |
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1. 1. The communication performance of 12 rhesus monkeys was investigated in a situation in which the rewards of both members of a pair of monkeys could not exceed chance levels unless the operator monkey responded to cues provided by the informant monkey which indicated the location of food. Each member of the pair was trained in both operator and informant roles in different phases of the experiment. Communication performance improved progressively to levels consistently above chance. However, communication learning appeared to be specific to the role in which the individual was trained, and when roles were reversed no evidence of transfer was obtained. Tests of foodsharing behaviour showed a substantial increase in the tendency to share food with the partner following communication training. This occurred however, only when the partner was the only social stimulus present; if another monkey was also present there was no evidence of preferential responses to the partner. In all phases of communication training, monkeys which were housed together performed more efficiently than did monkeys housed individually.2. 2. The acquisition of stimulus-producing responses was investigated by causing an opaque screen to remain in front of the informant unless the operator monkey pulled a vertical lever at the front of its restraining cage. Initially, operators responded immediately to the foodcarts, but with further testing there was a steady increase in the tendency to defer the response to the food-carts until the lever had been pulled, revealing the informant monkey.3. 3. Transfer of communication training was tested with new monkey informants, and with two inanimate stimuli, a mechanical puppet, and a stationary plaque. The latter two objects were placed behind the rewarded food-carts before each trial. There was clear evidence of positive transfer to each of these conditions, but marked differences among conditions were obtained. Performance with the monkeys averaged 76 per cent. correct, as compared with 62 and 40 per cent., with the puppet and the plaque, respectively.4. 4. To test the ability of trained operator monkeys to select the appropriate informant on the basis of behavioural cues, the communication situation was arranged so that two informant monkeys were present on all trials. However, on any trial only one of these informants could be rewarded, and the operator's rewards were contingent upon delivering food to this informant. Efficiency of discrimination began at approximately 45 per cent, (chance = 25 per cent. and improved progressively to levels above 75 per cent. |
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Equine Behaviour @ team @ |
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3017 |
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Schmidt, R.; Amrhein, V.; Kunc, H.P.; Naguib, M. |
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The day after: effects of vocal interactions on territory defence in nightingales |
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2007 |
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The Journal of Animal Ecology |
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T. J. Anim. Ecol. |
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76 |
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1 |
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168-173 |
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Aggression; Animals; Male; Songbirds/*physiology; *Territoriality; Time Factors; Vocalization, Animal/*physiology |
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1. Models on territory acquisition and tenure predict that territorial animals benefit by adjusting territorial defence behaviour to previous challenges they had experienced within the socially complex environment of communication networks. 2. Here, we addressed such issues of social cognition by investigating persisting effects of vocal contests on territory defence behaviour in nightingales Luscinia megarhynchos (Brehm). 3. Using interactive playback during nocturnal song of subjects, a rival was simulated to countersing either aggressively (by song overlapping) or moderately (by song alternating) from outside the subjects' territory. Thereby, the time-specific singing strategy provided an experimentally controlled source of information on the motivation of an unfamiliar rival. 4. Expecting that nightingales integrate information with time, the same rival was simulated to return as a moderately singing intruder on the following morning. 5. The results show that the vigour with which male nightingales responded to the simulated intrusion of an opponent during the day depended on the nature of the nocturnal vocal interaction experienced several hours before. 6. Males that had received the song overlapping playback the preceding night approached the simulated intruder more quickly and closer and sang more songs near the loudspeaker than did males that had received a song alternating playback. 7. This adjustment of territory defence strategies depending on information from prior signalling experience suggests that integrating information with time plays an important part in territory defence by affecting a male's decision making in a communication network. |
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Department of Animal Behaviour, Bielefeld University, PO Box 100 131, D-33501 Bielefeld, Germany. rouven.schmidt@uni-bielefeld.de |
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PMID:17184365 |
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Equine Behaviour @ team @ |
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2749 |
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Murray, Martyn G.; Brown, David |
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Title |
Niche Separation of Grazing Ungulates in the Serengeti: An Experimental Test |
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1993 |
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The Journal of Animal Ecology |
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T. J. Anim. Ecol. |
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62 |
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2 |
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380-389 |
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1. The niche separation of three species of alcelaphine antelope (wildebeest, topi and hartebeest) with similar body size was compared by measuring bite weight, bite rate, intake rate and selectivity of tame animals in plots containing grass at different growth stages. 2. On growing swards, hartebeest had a smaller bite weight and lower intake rate, and were also less selective of green leaf, than either topi or wildebeest. On senescent swards, hartebeest were more selective of leaf than the other two species. 3. Wildebeest had a faster bite rate than either topi or hartebeest on swards with low biomass and high protein content of green leaf (green flush). Bite weight and intake rate of wildebeest and topi were similar despite the difference in breadth of their incisor rows. 4. Topi were significantly more selective of green leaf than the other two species and were the only species to maintain a rapid bite rate on swards with high green leaf biomass. 5. The feeding experiments did not reveal significant cross-overs between species in the rate of food intake on different grass types, but each species was most proficient either in leaf selection or bite rate when feeding on grass swards in a particular growth stage. We suggest that growth stage is a primary determinant of niche separation. 6. In Serengeti, grazing ungulates which migrate are specialists of the earlier growth stages of grass which tend to be transient, while those that are residential specialize on late growth stages which are more enduring. The mobility of species, and the spatial and temporal dynamics of pastures containing different growth stages of grass, contribute to niche separation. |
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Equine Behaviour @ team @ |
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3544 |
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Mills, M.G.L.; Shenk, M.G.L. |
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Predator--Prey Relationships: The Impact of Lion Predation on Wildebeest and Zebra Populations |
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1992 |
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The Journal of Animal Ecology |
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T. J. Anim. Ecol. |
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61 |
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3 |
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693-702 |
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1. The role of lion Panthera leo predation in the dynamics of blue wildebeest Connochaetes taurinus and zebra Equus burchelli populations was investigated through simulation models. The data used in the models were from intensive observations over 4 years in the south-east of the Kruger National Park. 2. Population estimates of wildebeest and zebra were made from aerial surveys, sex and age ratios from ground counts. Lion numbers were determined from observations of marked and radio-collared animals. Predation was studied by following lions for continuous periods of up to 336 h. 3. Two models were constructed. Model 1 ascertained the number of killing lions (adult females) that could be supported by each prey population while remaining stable. A single model was constructed for the sedentary wildebeest population. A summer and winter model was constructed for the semi-migratory zebra population. The sensitivity of the parameters in the model was tested by changing their value by 10%. In model 2, the kill age structure for each species was changed to determine the number of killing lions the altered prey selection parameters could support. 4. There was no difference in the vulnerability of either species to predation. Zebra foals (<1 year) were killed more frequently than expected. No selection for sex or by season could be found for either species. 5. Model 1 predicted that the wildebeest population stabilizes with 7.7 killing lions, close to the number in the study area. The winter zebra population stabilizes with 6.8 killing lions and the summer zebra population with 19.4. Manipulation of kill rate followed by adult fecundity rate had the greatest effect on population size of both species. In model 2, wildebeest predation was made selective towards calves and zebra predation was made non-selective for sex and age. With these parameters the wildebeest population stabilizes with 10.7 killing lions and the zebra population with 5.4 in winter and 15.1 in summer. 6. The models suggest that lion predation affected wildebeest more severely than zebra during the study. This was through the way in which lions selected their prey, and because of the sedentary behaviour of the wildebeest, as opposed to the semi-migratory behaviour of the zebra. |
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Equine Behaviour @ team @ |
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2376 |
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Klingel, H. |
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Observations on social organization and behaviour of African and Asiatic Wild Asses (Equus africanus and Equus hemionus) |
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1998 |
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Applied Animal Behaviour Science |
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Appl Anim Behav Sci |
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60 |
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2 |
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103-113 |
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Equus africanus Equus hemionus Territoriality |
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1This paper appears with kind permission of Verlag Paul Parey, Berlin and Hamburg. It was originally published in Z. Tierpsychol., 44, 323-331 (1977), ISSN 0044-3573/ASTM-Coden: ZETIAG.1
Abstract
African and Asiatic Wild Asses (Equus africanus and Equus hemionus) live in unstable groups or herds of variable composition. Some of the adult stallions are territorial in large territories in which they tolerate other ♂♂. The territorial ♂♂ are dominant over all their conspecifics |
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0168-1591 |
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Equine Behaviour @ team @ |
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6173 |
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Call, J. |
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A fish-eye lens for comparative studies: broadening the scope of animal cognition |
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2002 |
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Animal Cognition |
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Anim. Cogn. |
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5 |
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1 |
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15-16 |
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Animals; Behavior, Animal/physiology; Cognition/*physiology; Fishes/*physiology; Species Specificity |
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? is the article no longer available? |
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call@eva.mpg.de |
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1435-9448 |
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PMID:11957396 |
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Equine Behaviour @ team @ |
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2616 |
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Crowell-Davis, S.L.; Houpt, K.A.; Carini, C.M. |
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Mutual grooming and nearest-neighbor relationships among foals of Equus caballus |
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1986 |
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Applied Animal Behaviour Science |
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Appl. Anim. Behav. Sci. |
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15 |
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2 |
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113-123 |
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A 3-year study was carried out on the developmental behavior of foals from birth to 24 weeks of age and the behavior of mares living with foals. Mutual-grooming partners of foals were primarily other foals. The peak frequency of mutual grooming occurred during Weeks 9-12, when fillies mutual-groomed 1.6 times h-1 and colts mutual-groomed 0.9 times h-1. Fillies mutual-groomed more frequently than colts (P < 0.025). Fillies mutual-groomed randomly with colts and other fillies (P < 0.05), whereas colts mutual-groomed almost exclusively with fillies (P = 0.03). At all ages studied, if a foal's nearest neighbor was not its mother, it was more likely to be another foal than would be expected if the foal was associating randomly with non-mother ponies. Fillies were more likely than expected to have a filly rather than a colt as their nearest neighbor (P = 0.01). Thus, during their first few months of life, the foals studied exhibited patterns of behavior which were consistent with the development of the usual social milieu of unmanaged adults, in which several mares form a cohesive herd with one or more stallions associating with them. |
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Equine Behaviour @ team @ |
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2276 |
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Anderson, M.K.; Friend, T.H.; Evans, J.W.; Bushong, D.M. |
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Behavioral assessment of horses in therapeutic riding programs |
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1999 |
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Applied Animal Behaviour Science |
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Appl. Anim. Behav. Sci. |
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63 |
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1 |
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11-24 |
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Horses; Therapeutic riding; Temperament; Cortisol; Catecholamines |
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A behavioral assessment of horses who were being used and not used in therapeutic riding programs was conducted to help determine useful methods of selecting horses for use in therapeutic riding programs. A total of 103 horses (76 horses from five therapeutic riding centers and 27 non-therapeutic riding horses from four sites) were used. Temperament survey for each horse were completed by three riding instructors at each therapeutic riding center or by the individual most knowledgeable about the horse at the other sites. Twenty personality traits from the survey were used to quantify temperament. Concentrations of plasma cortisol, norepinephrine and epinephrine were also measured in each horse. A reactivity test was then conducted which involved introducing three novel stimuli: a walking and vocalizing toy pig placed on a cardboard surface in front of the horse for 20 s; popping a balloon near the horse's flank area; and suddenly opening an umbrella and holding it open in front of the horse for 20 s. Reactions (expressions, vocalizations and movement) to each of the stimuli were scored and used to calculate an average reactivity score for each horse. The therapeutic riding instructors did not often agree on the temperament of their center's horses. The personality trait ratings made by the therapeutic riding instructors at each center were on average significantly correlated (P<0.01, r>0.52) for only 37.8% of the horses for any two instructors and 7.8% for three instructors. No significant correlations were found between temperament, reactivity, and the hormone concentrations (r<0.19), but regression analysis indicated a possibility of predicting temperament from the reactivity score and hormone concentrations (P<0.08). There was also a tendency for relationships between extremes in temperament (desirable vs. undesirable) and the hormone concentrations (P<0.09), and between extremes in reactivity (low vs. high) and the hormone concentrations (P=0.08). The difference in ratings among riding instructors indicates a need for more collaboration between instructors when evaluating horse temperament. This study also indicates that it was very difficult to objectively determine the suitability of horses for therapeutic riding programs regarding their temperament and reactivity, probably because other traits (e.g., smoothness of gait) are also considered very important. |
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Equine Behaviour @ team @ |
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4812 |
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