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Author |
McGreevy, P.D. |
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Title |
Development and Resolution of Behavioural Problems with the |
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Havemeier Workshop |
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The ideals of equestrian technique combine art and science. Therefore students of equitation
encounter measurable variables such as rhythm, tempo and impulsion alongside more ethereal ones
such as outline and harmony. This mixture accounts for many of the idiosyncrasies of equestrianism
including the subjective scoring of performance in dressage tests, the elusiveness of perfection even at
an elite level of competition and the difficulty of expressing equestrian technique in empirical terms
(Roberts, 1992).
This chapter will describe and offer examples of the unwelcome behavioural responses horses
produce under saddle. Two broad sections are then proposed to allow the reader to consider
unwelcome behavioural responses caused directly by humans as distinct from those attributable more
to the horse than the rider. Ultimately the responsibility for problems in the ridden horse lies with
humans since we have undertaken the domestication and exploitation of equids. Therefore it is
accepted that the dichotomy is not absolute. The chapter closes with a |
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471 |
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Author |
Linklater, W. L.; Cameron, E. Z.; Stafford, K. J.; Minot, E. O. |
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Title |
Estimating Kaimanawa feral horse population size and growth |
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SCIENCE & RESEARCH INTERNAL REPORT 185 |
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Animal flight behaviour in response to aircraft could have a profound influence
on the accuracy and precision of aerial estimates of population size but is rarely
investigated. Using independent observers on the ground and in the air we
recorded the presence and behaviour of 17 groups, including 136 individually
marked horses, during a helicopter count in New Zealand’s Kaimanawa
Mountains. We also compared the helicopter count with ground-based
estimates using mark-resight and line-transect methods in areas ranging from
20.5 to 176 km2. Helicopter counts were from 16% smaller to 54% larger than
ground-based estimates. The helicopter induced a flight response in all horse
groups monitored. During flight, horse groups traveled from 0.1 up to 2.75 km
before leaving the ground observer’s view and temporarily changed in size and
composition. A tenth of the horses were not counted and a quarter counted
twice. A further 23 (17%) may have been counted twice but only two of the
three observers’ records concurred. Thus, the helicopter count over-estimated
the marked sub-population by at least 15% and possibly by up to 32%. The net
over-estimate of the marked sub-population corresponded to the 17% and 13%
difference between helicopter counts and ground-based estimates in the central
study area and for the largest area sampled, respectively. Feral horse flight
behaviour should be considered when designing methods for population
monitoring using aircraft. We identify the characteristics of the helicopter
count that motivated horse flight behaviour. We compared our own recent
estimate of population growth from measures of fecundity and mortality (λ =
1.096 with an earlier-published one (λ = 1.182, where r = 0.167) that had been
derived by interpolating between the available history of single counts. Our
model of population growth, standardised aerial counts, and historical estimates
of annual reproduction suggest that the historical sequence of counts since
1979 probably over-estimated growth because count techniques improved and
greater effort was expended in successive counts. We used line-transect, markresight
and dung density sampling methods for population monitoring and
discuss their advantages and limitations over helicopter counts. |
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Author |
Asa Cs, |
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Title |
Sociosexual behavior in the domestic pony |
Type ![sorted by Type field, ascending order (up)](img/sort_asc.gif) |
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1979 |
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Symposium on the Ecology and Behavior of Wild and Feral Equids |
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59-70 |
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Univ. of Wyoming. |
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Laramie |
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from Professor Hans Klingels Equine Reference List |
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900 |
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Author |
Krueger, K. |
![find book details (via ISBN) isbn](img/isbn.gif)
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Title |
Social learning and innovative behaviour in horses |
Type ![sorted by Type field, ascending order (up)](img/sort_asc.gif) |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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social learning, innovative behaviour, Equus caballus, cognitive capacities |
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The evaluation of important parameters for measuring the horses’ cognitive capacities is one of the central topics of the equine behaviour team at Nürtingen-Geislingen University. Social complexity has been said to be one of the settings in which needs for cognitive capacities arise in animals. A variety of studies throughout the last two decades proved the horses’ social complexity to be far more elaborate than previously assumed. Horses form social bonds for the protection of offspring, intervene in encounters of others, identify group mates individually and easily orientate in a fission fusion society.
In such socially complex societies, animals will benefit from learning socially. In many bird and primate species the degree of social complexity correlates nicely with the species abilities for social learning. Social learning was, therefore, argued to be an indicator for elaborate mental capacities in animals. We were delighted to prove that horses actually copy social behaviour and techniques for operating a feeding apparatus from older and higher ranking group members. In a recent study we found young horses, at the age of 3 to 12, to copy the operation of a feeding apparatus from a human demonstrator. Social learning seems to work nicely in horses when the social background of the animals is considered.
The degree to which individual animals adapt to changes in their social or physical environment by finding innovative solution appears to be the other side of the coin, of whether animals adjust to challenges by social learning. It is not very astonishing, that along with the animals’ social complexity and their ability to learn socially also the degree to which they show innovative behaviour was claimed to be one of the most important demonstrations of advanced cognitive capacities. In a recent approach, we started to ask horse owners and horse keepers in many countries to tell us about unusual behaviour of their horses via a web site (http://innovative-behaviour.org). To date, we received 204 cases of innovative behaviour descriptions from which six cases were clear examples of tool use or borderline tool use. We categorized the innovative behaviours into the classes, a) innovations to gain food, b) innovations to gain freedom, c) social innovations, d) innovations to increase maintenance, and e) innovations that could not be clearly assigned to a category. About 20% of the innovative horses showed more than one innovation. These animals could be termed “true innovators”. Again, young horses were more innovative than older ones with the age group 5 – 9 showing the highest number of innovative behaviour descriptions.
In a nutshell, the horses’ cognitive capacities appear to be underestimated throughout the last decades. The horses’ social complexity is far more elaborate than previously assumed, horses learn socially from conspecific and humans, some of them demonstrate innovative behaviour adaptations to their environment and even simple forms of tool use. |
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Krueger, K. |
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Xenophon Publishing |
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Wald |
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in prep |
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978-3-95625-000-2 |
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Equine Behaviour @ team @ |
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5848 |
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Author |
Keiper, R.R.; Moss, M.; Zervanos, S. |
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Title |
Daily and seasonal patterns of feral ponies on Assateague Island. |
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1980 |
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2nd Conference on Scientific Research in the National Parks |
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Equine Behaviour @ team @ |
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2310 |
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Author |
Whiten, A. |
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Social complexity and social intelligence |
Type ![sorted by Type field, ascending order (up)](img/sort_asc.gif) |
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2000 |
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Novartis Foundation Symposium |
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Novartis Found Symp |
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233 |
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185-96; discussion 196-201 |
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Animals; Brain/anatomy & histology/*physiology; Humans; *Intelligence/physiology; Learning; Models, Psychological; Primates; *Social Behavior; Social Problems |
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When we talk of the 'nature of intelligence', or any other attribute, we may be referring to its essential structure, or to its place in nature, particularly the function it has evolved to serve. Here I examine both, from the perspective of the evolution of intelligence in primates. Over the last 20 years, the Social (or 'Machiavellian') Intelligence Hypothesis has gained empirical support. Its core claim is that the intelligence of primates is primarily an adaptation to the special complexities of primate social life. In addition to this hypothesis about the function of intellect, a secondary claim is that the very structure of intelligence has been moulded to be 'social' in character, an idea that presents a challenge to orthodox views of intelligence as a general-purpose capacity. I shall outline the principal components of social intelligence and the environment of social complexity it engages with. This raises the question of whether domain specificity is an appropriate characterization of social intelligence and its subcomponents, like theory of mind. As a counter-argument to such specificity I consider the hypothesis that great apes exhibit a cluster of advanced cognitive abilities that rest on a shared capacity for second-order mental representation. |
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School of Psychology, University of St Andrews, St Andrews, Fife KY16 9JU, UK |
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1528-2511 |
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PMID:11276903 |
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2084 |
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Bos, H |
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Body condition scoring in free living Przewalski horses |
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The International Symposium of the Przewalski Horse |
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1999 |
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Askania Nova |
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Equine Behaviour @ team @ |
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2240 |
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No authors listed |
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Workshop on the geographic spread of Aedes albopictus in Europe and the concern among public health authorities. Proceedings of a workshop held at the Istituto Superiore di Sanita, Rome, Italy, 19-20 December 1994 |
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1995 |
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Parassitologia |
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Parassitologia |
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37 |
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2-3 |
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87-90 |
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*Aedes/growth & development/parasitology/virology; African horse sickness virus; Animals; Commerce; Dengue Virus; Dirofilaria; Disease Reservoirs; Ecology; Europe; Humans; *Insect Vectors/growth & development/parasitology/virology; Italy; *Mosquito Control/methods/organization & administration; Public Health; Rift Valley fever virus |
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0048-2951 |
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PMID:8778669 |
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Equine Behaviour @ team @ |
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2659 |
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[No authors listed] |
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International Conference on Environmental Cadmium: an overview |
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1979 |
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Environmental Health Perspectives |
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Environ Health Perspect |
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28 |
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297-30 |
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Animals; Cadmium/*toxicity; Cadmium Poisoning/metabolism; Congresses; Ecology; Environmental Exposure; Environmental Pollutants/*toxicity; Female; Forecasting; Haplorhini; Horses; Humans; Rats; Waste Disposal, Fluid |
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0091-6765 |
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PMID:39745 |
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Equine Behaviour @ team @ |
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2694 |
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Author |
McCall, C.A.; Hall, S.; McElhenney, W.H.; Cummins, K.A. |
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Title |
EVALUATION AND COMPARISON OF FOUR REACTIVITY TESTS IN HORSES |
Type ![sorted by Type field, ascending order (up)](img/sort_asc.gif) |
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2010 |
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Proc.17th Equine Nutr. Physiol. Symp |
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357 |
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Four methods of ranking horses on reactivity were evaluated and compared: isolation from conspecifics, presentation of a static novel stimulus, traversing a novel stimulus in a runway (isolation, novel stimulus and runways tests, respectively) and assigning subjective emotionality scores. Forty horses performed each of the three tests daily on three different days in a switchback design where treatments were injection of a tranquilizer or vehicle. Horses were randomly assigned a daily test sequence, which was maintained throughout the study. In all tests, heart rates were recorded and behavior was videotaped. To be considered a valid test of reactivity, at least one heart rate and one behavioural measurement in the test had to show a significant difference due to tranquilization, and behavioural measures had to be displayed in at least 75% of the trials. In the runway test, no significant difference in heart rate values in tranquilized and non-tranquilized horses was found, and no behavioural attribute was displayed in more than 52% of the trials; therefore it was rejected as a valid test of reactivity. Both isolation and novel stimulus tests produced valid measurements. Mean heart rate was the most precise physiological measure for these tests, and walking and defecation frequency were the most precise behavioural measures for novel stimulus and isolation tests, respectively. Mean heart rates on the novel stimulus and isolation tests were correlated (rs=0.79, P<0.01) indicating that these tests produced similar rankings based on physiological responses. However, behavioural measures ranked horses differently (rs=0.27, P<0.10) on the tests. Rank correlations between mean heart rates and behavioural measures were higher in the novel stimulus (rs = 0.66, P<0.01) than the isolation test (rs = 0.55, P<0.01), indicating that the novel stimulus test ranked horses based on either physiological or behavioural responses more similarly than did the isolation test. Therefore, the novel stimulus test was considered the more accurate evaluation of reactivity. Subjective emotionality scores were correlated moderately with mean heart rates (rs > 0.33, P<0.01) from the novel stimulus and isolation tests and with walking scores (rs = 0.47, P<0.01) from the novel stimulus test. Assignment of subjective emotionality scores was not as accurate as the novel stimulus or isolation tests in ranking horses for reactivity. Using physiological data alone, combining physiological and behavioural measurements or using more than one behavioural measurement in reactivity tests may reflect the reactivity of the horse better than a single behavioural measurement. |
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Lexington, KY |
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Equine Behaviour @ team @ |
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3689 |
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