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Author |
Krueger, K. |
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Title |
Social learning and innovative behaviour in horses |
Type |
Conference Article |
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Year |
2015 |
Publication |
Proceedings of the 3. International Equine Science Meeting |
Abbreviated Journal |
Proc. 3. Int. Equine. Sci. Mtg |
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Keywords |
social learning, innovative behaviour, Equus caballus, cognitive capacities |
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Abstract |
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 |
Schneider, G.; Krueger, K. |
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Title |
Third-party intervention |
Type |
Conference Article |
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Year |
2012 |
Publication |
Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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73 |
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Third-party intervention is the interruption of a dyadic interaction by a third animal. We observed such interventions in affiliative interactions in free-ranging Esperia-ponies (Equus caballus). It is known that horses intervene in affiliative contexts especially when a preferred partner is involved, probably to protect their social bond to this preferred partner. To prove this hypothesis the present study investigated whether the preferred partner was targeted, i.e. challenged, or supported by the intervener or both randomly. Therefore we examined the social relationship between the intervener and both dyadic interacting individuals. We found that interveners usually supported individuals to which they have stronger social bonds than to other group mates, while they have no particular relationship to the targeted animals. This indicates that interveners in stable horse groups protect their social bonds to the supported animals by challenging their interaction partners. Of all observed horses only some mares showed intervention behaviour. Their social position, reflected by their position in the dominance hierarchy, social networks, and the spatial group structure were investigated. We found that interveners occupy no unique position, but they are involved in a high amount of affiliative interactions, high-ranking, and relatively aggressive. KW - |
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Corporate Author |
Krueger, K. |
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Xenophon Publishing |
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Wald |
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978-3-9808134-26 |
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Equine Behaviour @ team @ |
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5549 |
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Author |
Komárková, M.; Bartošová, J. |
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Title |
Lateralized suckling in domestic horse foals (Equus caballus) |
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Conference Article |
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Year |
2012 |
Publication |
Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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in press |
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Keywords |
laterality; suckling; horse; foal |
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Animals with eyes placed laterally on their head would respond differently to stimuli detected on their different sides. Visual cues from the left eye are processed in the right hemisphere which controls the intensive emotion expression and fast response to the stimuli, while the left hemisphere receiving the information from the contralateral eye is responsible for the routine behaviour and concentration. Different use of left/right eye for exploring environment and evaluation of different stimuli was recently described in domestic horses. They use left eye predominantly for watching novel object or frightening stimulus which indicates specialization of right hemisphere (RH) for appraisal of these types of stimuli. We presumed such lateralisation also in foals during suckling when only monocular vision can be employed for observing surroundings (foals suck mostly in antiparallel body position). Two mutually exclusive hypotheses about the origin of probable foal’s preference for particular suckling side were postulated: 1) visual lateralization, then the foals should suck more often from the mother’s right side (‘from right’), so as potential danger would be detected by the better adapted right hemisphere (i.e. left eye); 2) motor lateralization (the analogous concept as human “handness”), then a foal should suck predominantly from one side, either left or right, more often. Within two seasons, suckling behaviour of 59 Kladruby mares giving birth to 79 foals was observed from deliveries to abrupt weaning (4-7 months of age). From 10 607 recorded suckling solicitations, 50.2% were performed from right, thus there was no preference of the suckling side on a population level. However, we found large variability in the probability of suckling from right among individual foals (p<0.0001); the probability ranged from 0.22-0.98. One third of the foals (35.4%) showed strong, either right (N=13) or left (N=15) side preference which further strengthened with age (interaction suckling side preference*foal’s age: p<0.0001). Other tested variables, i.e. sex of the foal, age of the mother and identity of the herd were not significant. The probability that the mother rejected foal’s suckling solicitation (N=108) did not differ according to the suckling side (right/left) or suckling side preference (right/left/no preference). Suckling bout duration was not significantly influenced neither by the suckling side nor suckling side preference regardless the mother or the foal terminated the suckling bout. In conclusion, only 16 % of the foals revealed significant right side preference for suckling while 19 % left side and 65 % no preference. Thus, we can reject the visual hypothesis because a general trait to suck with left eye open for better danger detection and recognition is unlikely to occur, at least in up to 7 months old foals. Such a young foal is probably fully focused on suckling and relies on mother’s vigilance. Observed individual side preferences indicated more likely a kind of motor lateralization in part of the foals. Further research is needed to clear up the effects of age and individual experience of the foal. Supported by AWIN, EU FP7 project No. 266213. |
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Komárková, M. |
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Xenophon Publishing |
Place of Publication |
Wald |
Editor |
Krueger, K. |
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978-3-9808134-26 |
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Equine Behaviour @ team @ |
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5505 |
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Author |
Klingel, H . |
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Title |
Social Organisation and Social Behaviour of the Equids |
Type |
Conference Article |
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Year |
2012 |
Publication |
Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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in press |
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In contrast to the great similarity in behaviour and ecology of the 6 extant Equid species, 2 distinct types of social organisation have evolved, and both are adapted to life in semi-arid to arid regions where environmental conditions force them to migrate seasonally or opportunistically.
The ranges of the various species overlap: Mountain Zebra Equus zebra and Plains Zebra E. quagga in South Africa and Namibia, Plains Zebra and Grevy's Zebra E. grevyi in Kenya and Ethiopia, Grevy's Zebra and African Wild Ass E. africanus in Ethiopia, Asiatic Wild Ass E. hemionus and Przewalski Horse E. przewalski in Mongolia and China. Although, in the overlap zones, individuals of the different species are using the same resources like water and grazing next to each other, they rarely make closer contacts.
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In the type 1 species, Horse, Plains Zebra and Mountain Zebra, the adults live in non-territorial, stable, one-male families and as single bachelors and in bachelor groups. Family stallions have the exclusive mating rights with the mares in their harems. These consist of up to 6 unrelated mares plus their offspring, totalling up to 20 members.
Mares stay in their harem until death. Stallions' tenure is from age 5-6 years, i.e. when they succeed in controlling a harem, for close to life time, but are replaced when dead or incapacitated. Harems are stable even in the absence of a stallion, indicating voluntary membership. Adolescent mares leave their parental families to become members of another harem.
In Plains Zebra the adolescent mares are abducted, during an oestrus, by suitors who fight the defending family stallion/father. Successful stallions are bachelors who start a family, or family stallions enlarging their harem. Young stallions leave their parental families voluntarily at age 2-3 years and join bachelor stallion groups from where the family stallions are recruited.
An individualised dominance hierarchy excists with the stallion in the alpha position. It is based on individual knowledge and recognition of the members.
In the type 2 species Grevy's Zebra, African Wild Ass and Asiatic Wild Ass adult stallions monopolise territories in which they have the exclusive mating rights. Stallions are tolerant of any conspecifics entering their territory. Bachelor stallions behave subordinately – or fight for the possession of the territory which is a prerequisite for reproduction.
Mares join up to form anonymous and unstable groups or herds. The only stable unit is of a mare and her offspring. In Grevy's Zebra mares with foal join preferentially conspecifics of the same soial status, as do mares without foal.
Matings take place inside the territory. There is no lasting relationship of the mare with a particular stallion, and the mare may be mated by any stallion whose territory she is visiting.
Territories measure up to 10 or more square kilometres, and tenure is for several years.
Grevy Zebra territorial owners leave their territories for a few hours to visit a water hole, or for months when grazing and water conditions are below requirements, and re-occupy it upon return, unchallenged. |
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Corporate Author |
Klingel, H . |
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Publisher |
Xenophon Publishing |
Place of Publication |
Wald |
Editor |
Krueger, K. |
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978-3-9808134-26 |
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IESM 2012 |
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Notes |
Invited speaker IESM 2012 |
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Call Number |
Equine Behaviour @ team @ |
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5436 |
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Author |
Klingel, H . |
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Title |
Soziale Organisation und Sozialverhalten der Equiden |
Type |
Conference Article |
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Year |
2012 |
Publication |
Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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in press |
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Verhalten und Ökologie der 6 rezenten Equiden sind in vieler Hinsicht identisch, jedoch in der Sozialen Organisation haben 2 deutliche verschiedene Formen evoluiert, die beide an das Leben in den semi-ariden und ariden Lebensräumen angepasst sind, wo sie zu säsonalen oder opportunistischen Wanderungen gezwungen sind.
Die Verbreitungsgebiete der verschiedenen Arten überlappen, in Südafrika und Namibia von Bergzebra Equus zebra und Steppenzebra E. quagga, in Kenya und Äthiopien von Steppenzebra und Grevy-Zebra E. grevyi, in Äthipien und Somalia von Grevy-Zebra und Afrikanischem Wildesel E. africanus, in China und der Mongolei Asiatischer Wildesel E. hemionus und Przewalski-Pferd E. przewalskii. Obwohl die Vertreter der verschiedenen Arten in den Überschneidungsgebieten die gleichen Ressourcen wie Wasser und Weide nutzen, nehmen sie kaum Kontakt zueinander auf.
Die Vertreter von Typ 1, Steppenzebra Equus quagga, Bergzebra E..zebra, Pferd E przewalskii, leben in nicht-territorialen , dauerhaften 1- Hengst- Familien, in Hengstgruppen und als Einzelgänger.. Die Familienhengste haben die alleinigen Paarungsrechte mit den Stuten in ihrem Harem. Dieser besteht aus bis zu ca. 6 nicht-verwandten Stuten nebst ihren Nachkommen und kann bis 20 Mitglieder haben.
Stuten bleiben bis zu ihrem Tod im Harem..Hengste können mit 5-6 Jahren einen Harem erobern oder gründen, können gleichfalls bis zum Tod die Familie begleiten, werden aber meist vorher von einem anderen Hengst ersetzt. Harems sind auch ohne Hengst stabil, ein Hinweis, dass die Stuten freiwilling im Harem sind und bleiben.. Junge Stuten verlassen ihre elterliche Familie und schliessen sich einem anderen Harem an..Beim Steppenzebra werden die Jungstuten während eines Östrus (Rosse) von Bewerbern entführt, gegen den Widerstand des Familenhengstes = Vaters. Bewerber sind Junggesellen, die so eine Familie gründen, und Familienhengste, die so ihren Harem vergrössern. Junghengste verlassen mit 2-3Jahren ihre elterliche Familie und schliessen sich Jungesellengruppen an, aus denen sich die Familenhengste rekrutieren.
In der Gruppe besteht eine Rangordnung mit dem Henst in der alpha-Position. Sie beruht aud individuellem Kennen und Erkennen der Mitglieder.
Bei Typ 2, Grevy-Zebra, Afrikanischer und Asiatischer Wildesel, monopolisieren Hengste über Jahre Territorien von 10 und mehr km2 , in denen sie die alleinigen Paarungsrechte haben. Territoriale Hengste tolerieren Artgenossen, auch erwachsene Hengste, soweit diese sich unterlegen verhalten. Oder sie stellen sich zum Kampf um den Besitz des Territoriums, eine Vorbedingung für die Fortpflanzung. Stuten im Östrus können von mehreren Hengsten begattet werden, wenn sie sich in deren Territorien aufhalten bzw diese durchwandern.
Stuten und Fohlen und nicht-territoriale Hengste schliessen sich zu anonymen instabilen Gruppen oder Herden zusammen. Feste dauerhafte Bindungen bestehen nur zwischen Stute und Fohlen. Hengste verlassen ihr Territorium für Stunden, Tage, im Extrem auch Monate, um zu Wasserstellen oder Weidegründen zu ziehen, sind aber bei Rückkehr wieder unangefochtene Besitzer. |
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Corporate Author |
Klingel, H . |
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Publisher |
Xenophon Publishing |
Place of Publication |
Wald |
Editor |
Krueger, K. |
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Deutscht |
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978-3-9808134-26 |
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IESM 2012 |
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Public Day |
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Equine Behaviour @ team @ |
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5437 |
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Author |
Kaplan, G. |
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Title |
Social animals and Communication, with special reference to horses |
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Conference Article |
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2015 |
Publication |
Proceedings of the 3. International Equine Science Meeting |
Abbreviated Journal |
Proc. 3. Int. Equine. Sci. Mtg |
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Kaplan, G. |
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Xenophon Publishing |
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Wald |
Editor |
Krueger, K. |
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Proc. 3. Int. Equine. Sci. Mtg |
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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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5796 |
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Kampmann, S.: A., Hampson, B.A.; Pollitt, C.C. |
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Title |
Population dynamics of Australian feral horses in a semiarid environment |
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Conference Article |
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Year |
2012 |
Publication |
Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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in press |
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Introduction: The feral horse population of Australia is the largest in the world and, in average seasons, increases at a rate of approximately 20% per annum. Recent record rainfall in much of semi-arid Central Australia has led to a population increase in excess of normal rates and this project aimed to document the increase. Uncontrolled feral horse numbers have habitat degradation and horse welfare implications and were the reasons for performing the study. Materials and Methods: The study area was an unmanaged 4,000km2 semi-arid area in Central Australia (Lat 24.50, Long 132.10). The population of feral horses within the study area is estimated to be in excess of 10,000. During an 8 week period at the end of the winter season of 2011, horses were identified by ground searches, movement sensored cameras and from hides positioned at key water holes. The area surveyed represented only a small percentage of the overall habitat. Horses were identified by descriptive features and markings. Where possible, sex and age category were documented. Population growth rate was estimated from the observed sample and was expressed as the number of foals born in the current year, divided by the number of horses older than one year. Results: A total of 1,486 horses were identified and categorised, of which 335 were foals born within the current foaling season. Only 129 juveniles, presumably born in the preceding year, were identified. Of the adult horses, 54% were male and 46% were female. Seventy-four percent of mares (n=452) had a foal at foot and the population growth rate was 29%. Conclusion: With a sustained population growth rate of 29%, this population of feral horses will more than double within 3 years. The high rate of increase is concerning because it will negatively impact on the native fauna and flora and fragile semi-arid ecosystems of Central Australia. In addition the feral horses of the study area have experienced an unusual period of high rainfall and plentiful grazing but a return to normal drought conditions is imminent. Starvation, thirst and death from diminished resources will then be a serious welfare concern for horses. KW - |
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Kampmann, S. |
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Xenophon Publishing |
Place of Publication |
Wald |
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Krueger, K. |
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Equine Behaviour @ team @ |
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5531 |
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Author |
Kaczensky, P. |
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Title |
Conservation of Asiatic wild asses |
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Conference Article |
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2015 |
Publication |
Proceedings of the 3. International Equine Science Meeting |
Abbreviated Journal |
Proc. 3. Int. Equine. Sci. Mtg |
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Kaczensky, P. |
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Xenophon Publishing |
Place of Publication |
Wald |
Editor |
Krueger, K. |
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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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5839 |
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Author |
Jacquot, M.; Grosjean, A., Emrot, C.; Van-Erck-Westergem, E.; Schwartz, C.; Tomberg, C. |
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Title |
Effects of a walk phase at the warm up onset on physiological and behavioural parameters of ridden horses (Equus caballus) |
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Conference Article |
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2015 |
Publication |
Proceedings of the 3. International Equine Science Meeting |
Abbreviated Journal |
Proc. 3. Int. Equine. Sci. Mtg |
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Abstract |
For human athletes, any physical performance classically begins with a warm-up including a phase of cardio-respiratory activation as well as a phase of neuro-muscular mobilization. For the equine athletes similar routines are widely followed despite limited scientific studies addressing its effectiveness. Although physiological bases are of a similar nature in humans and horses, the latter are showing a different “telos” related to their status of prey. Indeed, their survival depends on their ability to detect any predator or potential danger in their environment and to estimate the need to run away. Therefore warm-up techniques should be adapted to this specificity and we added a walk phase preceding the usual warm-up during which the horse was allowed to visually assess its environment without constraint imposed by its rider, reins being long. We assumed that this walk phase would allow a more relaxed mental state and then a decrease in cognitive resources involved in environmental monitoring. Consequently this would release cognitive resources then available for the communication between the horse and the rider.
The autonomous nervous system (ANS) regulates the heart rate via the sympathetic and the parasympathetic nervous systems. The sympathovagal balance and the heart rate variability are considered as good indicators of an acute stress state as well as emotional states. These measures are frequently used to estimate well-being in animals. During the walk phase, we observed a significant decrease of the heart rate (HR), a significant increase of its variability and a significant modification of the sympathovagal balance in favour of a higher contribution of the parasympathetic control. We also measured the non-linear correlation dimension which reflects the degree of freedom of a system. To the best of our knowledge, this method was used until now only in humans to whom it was shown that its decrease is related to stressful events and is associated with a bad prognosis for survival. During the walk phase in horses, the dimension of correlation of cardiac activity was increased.
From a behavioural point of view, we observed a significant decrease of side movements related to head orientation as well as significant changes in ears position, the latter being preferentially directed forwards at the beginning of the walk phase and laterally at the end. As previous research suggests that ears position and head orientation can be involved in attentional mechanisms in horses, our results suggest a decrease of the attention focused on the environment. Furthermore, a significant lowering of the neck was observed as well as a significant decrease of behaviours related to stress.
To conclude our results suggest that a walk phase preceding the usual warm-up of horses would contribute to improve their mental state in favour of more relaxation and of a decrease of the attentional resources invested in environmental monitoring. |
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Jacquot, M. |
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Xenophon Publishing |
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Wald |
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; Krueger, K. |
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978-3-95625-000-2 |
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Equine Behaviour @ team @ |
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5897 |
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Author |
Merkies, K.; Isensee, A.; MacGregor, H.; Koenig von Borstel, U.; Tucker, A.; Carson. J.; Bergeron, R. |
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Title |
Influence of psychological and physiological arousal in humans on horse heart rate and behaviour |
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Conference Article |
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2012 |
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Proceedings of the 2. International Equine Science Meeting |
Abbreviated Journal |
Proc. 2. Int. Equine. Sci. Mtg |
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in press |
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Keywords |
horse-human interaction, heart rate, behaviour, human nervousness |
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Abstract |
The interaction of horses with humans is a dynamic state, but it is not clearly understood how horses perceive humans. Nervousness is transmissible from humans to horses indicated by increased horse heart rate (HR), however no studies have investigated whether horses can differentiate between humans who are physiologicallystressed (eg. after exercising) as opposed to psychologically-stressed (eg. feeling nervous/afraid). Horses (N=10) were randomly subjected to each of four treatments: 1) no human [control], 2) a calm human comfortable around horses [CALM; N=2 humans], 3) a physically-stressed human [PHYS; human exercised to reach 70% of maximum HR; N=2 humans], and 4) a psychologically-stressed human [PSYCH; human who was nervous around horses; N=14 humans]. Humans ranked themselves on a scale of 1-10 for their nervousness around horses. Both humans and horses were equipped with a HR monitor. Behavioural observations of the horses [gait, head position relative to the withers, distance from human, orientation toward human] were recorded live. Horses were allowed to wander loose in a round pen for 5 minutes of baseline recordings, at which time the human subject entered the round pen, stood in the centre and placed a blindfold over his/her eyes. The human remained in the centre of the round pen for an additional 5 minutes. Horse HR during control did not differ from when the human was present in the CALM and PSYCH treatment, and was lower during the PHYS treatment (51a vs 54a vs 55a vs 45b bpm for control, CALM, PSYCH and PHYS respectively; a,b differ p<0.0001). Over the 5 minute test period, horse HR decreased in PHYS and PSYCH (p<0.01) whereas it increased in CALM (p<0.0001). Horse HR decreased with increasing human rank of nervousness around horses (p=0.0156), and horses stood nearer to the human when they faced the human (p<0.0001) regardless of treatment. Horses moved at a faster gait in the control treatment, and their gait was slowest in the PSYCH treatment (p<0.0001), and the horse’s head position was lower in the PHYS and PSYCH treatments compared to CALM or baseline (p< 0.0001). A lower horse head position was positively correlated to a lower horse HR (p<0.0001) and negatively correlated to horse age (p<0.0001). Human HR was affected by treatment, with PHYS having the highest HR (p<0.0001). Human HR increased when the horse was facing away from the human, even though the human was blindfolded (p=0.0395). Overall, horses appear to be influenced by the physiological and psychological state of a human without any direct contact. Horses’ posture does reflect their physiological state. Understanding how horses react to human physiological and psychological states is especially important in equine-assisted activities, where the response of the horse has specific implications for the human participant. |
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Corporate Author |
Isensee, A. |
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Publisher |
Xenophon Publishing |
Place of Publication |
Wald |
Editor |
Krueger, K. |
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978-3-9808134-26 |
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Equine Behaviour @ team @ |
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5545 |
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