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Bartos, L., Bartosova, J., Pluhacek, J., & Sindelarova, J. (2012). Promiscuous behaviour disrupts pregnancy block in domestic horse (Equus caballus) mares: A counterstrategy against possible male infanticide. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: It is a common practice that the domestic horse mare is removed from her home environment and transported elsewhere for mating. After conceiving she is returned back into her home environment and social group, containing often familiar stallions and geldings. If we presume that the behavioural adaptation for infanticide relevant for wild, or free-ranging horses has not be lost in domestication (and it is clear that it remains at least within feral populations), then we may expect that, unless prevented by fencing or other management measures, the dominant males in the home social group may subsequently attempt infanticide. Foetal loss is a common phenomenon in domestic horses, being usually substantially higher than that in other domestic ungulates reaching up to 40%. One adaptive response to infanticide risk in polygynous populations is the Bruce effect. Pregnant females terminate their pregnancies when exposed to a dominant strange male. Our previous studies on plain zebra suggested the possibility of the Bruce effect also in equids. In this study we therefore tested the presumption that the Bruce effect could explain foetal loss in domestic horses. Based on reproduction records from horse breeders, we have recently published that bringing a pregnant mare which had been mated away from home into a vicinity of a familiar male who was not the father of her foetus increased probability of pregnancy disruption (Behav Ecol Sociobiol DOI: 10.1007/s00265-011-1166-6). These mares aborted in 31% of cases, while none of those mated within the home stable aborted. Repeated sexual activity either by a stallion or dominant gelding from the normal home group was observed shortly after the mare came from away-mating. Pregnant mares isolated from home males by a fence were even seen soliciting them over the fence. Therefore, there is probably some other mechanism than the Bruce effect leading to pregnancy block in the mare. We speculate that, once returned to the home “herd”, and introduced to familiar males, mares were more likely to terminate their pregnancy to save energy and avoid likely future infanticidal loss of their progeny by dominant male(s) of the home social group. Additional data has now showed that if a mare was mated away from home and was brought into an environment containing mares only, she was less likely to abort than a mare returning to an environment containing familiar male or males. This further supports our above hypothesis. Supported by AWIN, EU FP7 project No. 266213.
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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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Lovrovich, P., Sighieri, C., & Baragli, P. (2012). The human-given cues and behavioural plasticity of horses during a delayed three choice task. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Recent studies have tested the ability of horses to understand human gestures. But even at the moment results are rather contradictory. This study was aimed at analyzing ability of horses to understand, remember and use human-given cues in a delayed three choice task. After the training period, sixteen horses had to choose between three blue buckets. One of them hid a carrot. Eight horses (A-group) saw the person hiding the carrot and they had to choose the correct bucket only after the person had hidden carrot and gone away. Control group, eight horses (B-group) did not know where the carrot was, and could only choose the bucket through the use of smell or by random choice. Each horse carried out 10 trials in the same test session. A-group chose the correct bucket to a greater extent on the first try (4.37±1.42), compared to the second (3.00±0.53) and the third try (0.75±0.71). With significant differences between the first and the second try (t14=2.582, p=0.022), the first and the third try (t14=6.508, p=0.000), and between the second and the third try (t14=7.180, p=0.000). Also the B-group chose the correct bucket to a greater extent on the first try (3.87±0.83) compared to the second (3.37±1.51) and the third (1.75±1.49). Anyway, there was no differences between the first and the second try (t14=0.821, p=0.425). As regards the B-group, statistical differences were found between the first and the third try (t14=3.523, p=0.003) and between the second and the third try (t14=2.171, p=0.048). Moreover, A-group showed a negative correlation (r=-0.652, p=0.0409) between the number of correct answers at first trial, and seemed that they used human information during the first half of the trials. As the trials proceeded, the average time required to find carrot decreased, with a negative correlation (r=-0.779, p=0.0079) over trials while, the number of overturned bucket to find carrot increased over trials (r=0.770, p=0.0091). As the trials proceeded, the horses tended to choose at first the bucket where the carrot had been found in the previous trial (r=0.450, p=0.013). Any kind of correlation over trials was found in B-group. In the first trials, the horses we studied seemed to understand human given-cues information, store it and use it appropriately even in absence of a person. As trials proceeded they seemed to change strategy, searching carrots where it had been found in the previous trial. Therefore, horses could use human given-cues or other cognitive strategy depending on the time, energy cost and mental effort required to solve the task. KW -
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Mezei, A., Posta, J., & Mihók, S. (2012). Analysis of eventing competition results of Hungarian Sporthorses. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: The aim of the study was to evaluate the Hungarian Sporthorse population based on eventing competition performance. The database contained the results of 792 horses and 449 riders between 1996 and 2006. The eventing results were gathered from Hungary and other European countries. Blom transformed ranks were used to measure competition performance. Sporthorses competed in fourteen categories but only the easiest category (category ’A’) contained enough result to handle it as a single category (model I.). The other 13 categories were handled together based on professional reasons in a different model (model II.). In model III., all records were analysed together and the results were weighted according to the difficulty of the category. The competition results were classified into eight groups, each group had a weight (0-7) and it was multiplied by a constant 3, and the result of this formula was added to the original Blom score. The linear mixed models included fixed effects for age, sex, breeder, owner, location, year and random effects for animal and rider. The model II. contained one more fix effect for difficulty of the competition level. The distribution of number of horses and number of starts by sex were heterogeneous (P<0.05). For category ’A’ mares and geldings appeared in higher proportion, despite this fact ratio of stallions is greater in higher competition levels. Considering the goodness of fit in each model, model fitting to the weighted Blom scores was the best R2=0.82. In model III. every fix effects (age, sex, breeder, owner, location, year) were significant. Random effects for animal and rider were not significant, but form professional point of view they need to be included in the model. The variance components estimated for the weighted Blom scores were the highest also (0.52 rider effect, 0.09 animal effect), the animal x rider interaction effect was zero. The variance proportion of rider effect exceeded the variance proportion of animal effect in each model. Breeding values of eventing performance were predicted using model III. The reliability of the estimated breeding values was acceptable for only a few stallions. To improve the reliability of breeding values, more progenies should be used in eventing competitions (as a kind of progeny test) and more competition records needed (as a kind of own performance test).
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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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Becker-Birck, M., Biau, S., Aurich, C., Möstl, E., Ille, N., & Aurich, J. (2012). Heart rate and heart rate variability in the horse and its rider: different responses to training and a public equestrian performance. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: While detailed information exists on the cardiovascular response of horses to racing or endurance, much less is known about cardiovascular function of the rider in equestrian sports. Combined analysis of the horse-rider-team has not been investigated so far. In this study, we have analyzed changes in heart rate and heart variability (HRV) variables SDRR (standard deviation of beat-to-beat interval) and RMSSD (root mean square of successive beat-to-beat intervals) both in well-trained horses (n=9) and their highly experienced riders (n=7) during the airs above the ground (sauteurs en liberté of the Cadre noir de Saumur) at a public performance and at an identical, but non-public training session, both lasting for exactly 7 min. Heart rate in the horses and riders increased during the airs above the ground, both in training and in the public performance (p<0.001 over time). In the horses, this increase did not differ between training and public performance (training: from 35±6 in the stable to 97±17 beats/min during riding, performance: from 43±13 to 103±13 beats/min, respectively). In contrast, in the riders, the increase in heart rate was significantly more pronounced (p<0.01) during the public performance (basal value 91±10, maximum 150±15 beats/min) than during training (basal value 94±10, maximum 118±12 beats/min). With regard to HRV in horses, overall SDRR did not change significantly over time and did not differ significantly between training and performance. RMSSD decreased during both training and performance to the same extent, indicating a decrease in parasympathetic (vagal) tone. In the riders, both HRV variables decreased significantly during riding (p<0.001) and for SDRR the decrease was more pronounced (p<0.05) during an equestrian performance compared to a training session. During the performance SDRR decreased from a basal value of 5.0±1.5 to a minimum of 3.2±0.6 msec while respective values for the training session were 5.3±1.1 and 2.3±1.1 msec. Both a public performance and an identical training session of the airs above the ground in the ridden horse caused an increase in heart rate and a decrease in HRV variables. While increases in heart rate are mainly caused by physical activity, decreases in HRV also indicate a stress response. The cardiovascular response in the horses did not differ between a training session and a public performance but clear differences could be demonstrated in the riders. During a public performance, the increase in heart rate and decrease in SDRR were more pronounced than during a similar training session. In conclusion, the presence of an audience thus causes more pronounced sympathoadrenal activity in experienced riders than the same equestrian tasks ridden without spectators present. In contrast, the presence of an audience was without effect on sympathoadrenal activity in experienced horses. KW -
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Flauger, B., Möstl, E., & Krueger., K. (2012). The introduction of horses into new groups: Social interactions and cortisol release. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Domestic horses are kept in so-called “fate societies” where they have to deal with frequent mixing. Several studies have evaluated and discussed the aggression level and injury risk during the introduction of horses into new groups, but nothing is known about the endocrine responses and thus if horses experience stress during introduction.
In this study we analysed the efficiency of four approved introduction techniques and evaluated the introduction of 30 horses into 11 different groups. Horses were introduced: 1) immediately, 2) after observing the new group for several days, 3) together with an “integration horse” after several days of observation, or 4) with a mixed strategy. Aggressive as well as positive social behaviour between the introduced horses and the group members were analysed the two hours following the introduction event. In addition, we focussed on the glucocorticoid production of the newcomer horses by measuring faecal cortisol metabolites (FCM) on the day of the introduction as well as the following three days.
For the four introduction techniques we found significant differences in the horses’ aggressive and submissive behaviour as well as in their total interactions. The introduction together with an integration horse led to significantly lower levels of aggression and less total interactions than the immediate introduction of single horses.
Horses which were introduced immediately or after an observation period showed significantly elevated levels of FCM on the first, second and third day after the introduction. For horses introduced together with an integration horse FCM were already significantly higher on the day of the introduction, indicating a stressful event before the introduction itself. In contrast, FCM levels were always very low when using the mixed technique.
In sum, horses have the ability to deal with conflict when they are introduced to new group members. The introduction event itself appears not to be as stressful as previously assumed. Standing together with an “integration horse” on a separate paddock and not being able to integrate immediately into a new group appears to be stressful for the newcomer. Based on the findings of our study we suggest to introduce new horses in group management together with a new group mate, a so-called “integration horse”. This would reduce the number of total social interactions as well as the aggression level. While this technique may be stressful for the newcomer, it lowers aggressive behaviour between the introduced horse and the group members and consequently reduces injury risks.
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Houpt, K. A. (2012). Horse husbandry and equine stereotypies. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
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Hampson, B. A., de Laat, M. A., Mills, P. C., & Pollitt, C. C. (2012). Distances travelled by feral horses in ‘outback’ Australia. In K. Krueger, & (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Summary Reasons for performing study: The distance travelled by Australian feral horses in an unrestricted environment has not previously been determined. It is important to investigate horse movement in wilderness environments to establish baseline data against which the movement of domestically managed horses and wild equidae can be compared. Objectives: The aim of this study was to determine the travel dynamics of two groups of feral horses in unrestricted but different wilderness environments. Methods: Twelve feral horses living in two wilderness environments (2,000 km2 vs. 20,000 km2) in outback Australia were tracked for 6.5 consecutive days using custom designed, collar mounted global positioning systems (GPS). Collars were attached after darting and immobilising the horses. The collars were recovered after a minimum of 6.5 days by re-darting the horses. Average daily distance travelled was calculated. Range use and watering patterns of horses were analysed by viewing GPS tracks overlaid on satellite photographs of the study area. Results: Average distance travelled was 15.9 ± 1.9 km/day (range 8.1-28.3 km/day). Horses were recorded up to 55 km from their watering points and some horses walked for 12 hours to water from feeding grounds. Mean watering frequency was 2.67 days (range 1 – 4 days). Central Australian horses watered less frequently and showed a different range use compared to horses from central Queensland. Central Australian horses walked for long distances in direct lines to patchy food sources whereas central Queensland horses were able to graze close to water sources and moved in a more or less circular pattern around the central water source. Conclusions: The distances travelled by feral horses were far greater than those previously observed for managed domestic horses and other species of equidae. Feral horses are able to travel long distances and withstand long periods without water allowing them to survive in semi-arid conditions.
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Rubenstein, D. (2012). Wild Equid Movements: Impacts of Habitat Quality, Predation Pressure and Leadership. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Animals spend much of their lives on the move searching for food, shelter and mates. As long-legged, large bodied species, equids are well suited for traveling long distances. Understanding where free-ranging equids go, why they choose particular locations, some near and some far, and what impact such movements have on patterns of sociality, demography and human livelihoods are only now coming into focus. This talk will explore how bottom-up factors, such as the abundance and distribution of key resources, and top-down factors, such as the type and location of predators, interact to shape overall movement patterns of equids, how leadership roles develop and what outcomes such movements are likely to have on human activities.
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