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Merkies, K., Isensee, A., MacGregor, H., Koenig von Borstel, U., Tucker, A., Carson. J., et al. (2012). Influence of psychological and physiological arousal in humans on horse heart rate and behaviour. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
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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Kampmann, S.: A., Hampson, B.A., & Pollitt, C. C. (2012). Population dynamics of Australian feral horses in a semiarid environment. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: 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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Klingel, H.. (2012). Social Organisation and Social Behaviour of the Equids. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: 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. . 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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Klingel, H.. (2012). Soziale Organisation und Sozialverhalten der Equiden. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: 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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Komárková, M., & Bartošová, J. (2012). Lateralized suckling in domestic horse foals (Equus caballus). In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: 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.
Keywords: laterality; suckling; horse; foal
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Schneider, G., & Krueger, K. (2012). Third-party intervention. In Proceedings of the 2. International Equine Science Meeting (73). Wald: Xenophon Publishing.
Abstract: 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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Krueger, K. (2012). Konfliktlösungsstrategien der Menschen und Pferde. In Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Abstract Missing KW -
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Kultus, K., & Balzer, H. - U. (2012). Untersuchungen zur Mensch-Pferd-Beziehung. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Abstract Missing KW -
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Kultus, K. B., & Balzer, H. - U. (2012). Analysis of Human-Horse-Relation. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The relation between humans and animals is one of the most famous factors for animal welfare in modern housekeeping systems. Words like intuition and empathy in exposure to the horse are difficult to describe, to measure or to teach. In German speaking countries there is the sentence: a good rider knows what the horse will do before it can do it; a bad rider only reacts to what the horse has done. By using the monitoring systemsmardwatch® in connection with chronobiological regulation diagnostics it becomes possible to get insight in the interaction between human and horse.Thesmardwatch® enables measuring of so called psycho-physiologicalparameters likeskin resistance, skin potential, electromyogram and skin temperature, measured 10 times per second; it also registersbehaviorinformation as 3D-acceleration and -position and over this environment information like temperature, noise and brightness. Cutting hooves, cleaning and riding a horse are monitored for example. The data were analyzed under distinct aspectsby chronobiological regulation diagnostics developed byBalzerand Hecht (2000). The physical and vegetative activities of the human and the animalwhere pointed out separately and in their interactionat different levels. Very interesting is the influence of different humans on one horse or the influence of one human on distinct horses. The synchronies or asynchronies in the behavior of different human-horse-pairs could be proved at the level of their vegetative functions. While riding phases of exhaustion of the horse could be shown just as the increasingactivity of the rider to compensate this exhaustion. The method could be a basic approach to develop new training methods which agree with individual rhythms of riders and horses to optimize their achievement.These analysis are not only important for riding, they also give useful directions for daily contact with horses. So it will be possible to detect harmony/disharmony between human and horse for their pairing in order to teach them and to buy or sell a horse, respectively. KW horse, human, chronobiology, synchronisation, smardwatch
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Lojek, J., Lojek, A., & Zielinska, A. (2012). Certain factors influencing the condition of free-ranging Konik Polski horses (Equus caballus) in the Bierza National Park. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The objective of the study was to analyze certain factors influencing the condition of free-ranging Konik Polski horses in a fenced area measuring 200 ha located in the Biebrza National Park (Biebrza NP). The Body Condition Scoring system (BCS) was used not only as means of assessment of health and fitness of the horses but also for evaluation of the quality and productivity of the grazing area selected for horses, as well as stocking rate. Body Condition Scoring was determine with a 9-point scale by averaging the scores that were assigned to each of the six body areas that are most responsive to changes of body fat (Hennecke, 1983). The condition of horses was assessed 7 times from February 2009 to December 2011 on a total of 59 horses (3 stallions (n= 12 observations), 21 females 3–8 year olds (n=81) and 35 youngsters (up to 2 year olds) (n=88). The number (from 1 to 3) and composition of family bands varied throughout the period of investigation. The horse population in the Biebrza NP consist of horses from 3 different breeding centers. The analysis of variance (GLM) was used to investigate the effects of the fixed factors – weather conditions, family band, breeder of the horses, age and sex, on the mean of BCS points of horses (SPSS, version 19.0). The most important factor influencing the condition of free-ranging Konik Polski horses in the Biebrza NP were weather conditions, what is shown by the data concerning temperature from 3-month period preceding condition scoring (P < 0.01). This factor influenced not only animals, but also vegetation characteristics. The highest BCS means of horses (5.09) were achieved when average temperature during the 3-month period preceding condition scoring amounted between +1 to +8°C, and was better than obtained when average temperature amounted +18°C (4.80). The last temperature seems too high for horses and can be connected also with other factors, like high incidence of insects which could deteriorate grazing activity of animals. The lowest BCS means (4.56) were obtained when mean temperature was below 0°C. Other factors had no significant effect on the BCS means. As concern to breeder, the highest BCS means achieved mares from Popielno (5.08) – the oldest Polish free-ranging population of Konik Polski horses, which confirms that horses from this breeding center are justly considered to be the toughest and well adapting to difficult environmental conditions. The horses from the Biebrza NP achieved also high BCS means (4.79) which prove that they were well suited to the specific conditions of this habitat, which is overgrown mostly with forest – 73,7%, and willow and birch shrubs – 13,3% of area. The grazing area measures about 40 hectares and consists of wetlands dominated by sedges (Carex sp.). The horses moved from the Seven Island Reservation to Biebrza NP achieved the poorest results as far as adaptation to the conditions of the new habitat, and reached the lowest BCS means (4.57). The youngest horses (up to 2 year olds), 3-5 year olds, and 6-8 year olds had similar BCS means (respectively 4.94, 4.83, 4.68) which indicates good acclimatization of horses from different age categories to the grazing resources in the Biebrza NP. The highest means achieved by youngest horses indicate important trait of Konik Polski horses – mare`s careful care of offspring. The BCS means of horses from different family groups show the highest value of horses from family group of the most experienced stallion – Mrok (4.97). In every BCS scoring, stallions achieved the highest means, which was the reason to exclude their results from analysis. The results of this study suggest that the Body Condition Scoring of horses in the Biebrza National Park depends primarily on the acclimatization of horses to harsh environmental conditions and less importantly to belonging to a specific breeder, family band, age or sex.
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