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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.
Abstract: Abstract KW -
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Schneider, A. - C., Melis, A. P., & Tomasello, M. (2012). How chimpanzees solve collective action problems. Proceedings of the Royal Society B: Biological Sciences, .
Abstract: We presented small groups of chimpanzees with two collective action situations, in which action was necessary for reward but there was a disincentive for individuals to act owing to the possibility of free-riding on the efforts of others. We found that in simpler scenarios (experiment 1) in which group size was small, there was a positive relationship between rank and action with more dominant individuals volunteering to act more often, particularly when the reward was less dispersed. Social tolerance also seemed to mediate action whereby higher tolerance levels within a group resulted in individuals of lower ranks sometimes acting and appropriating more of the reward. In more complex scenarios, when group size was larger and cooperation was necessary (experiment 2), overcoming the problem was more challenging. There was highly significant variability in the action rates of different individuals as well as between dyads, suggesting success was more greatly influenced by the individual personalities and personal relationships present in the group.
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MacLean, E., Matthews, L., Hare, B., Nunn, C., Anderson, R., Aureli, F., et al. (2012). How does cognition evolve? Phylogenetic comparative psychology. Anim. Cogn., 15(2), 223–238.
Abstract: Now more than ever animal studies have the potential to test hypotheses regarding how cognition evolves. Comparative psychologists have developed new techniques to probe the cognitive mechanisms underlying animal behavior, and they have become increasingly skillful at adapting methodologies to test multiple species. Meanwhile, evolutionary biologists have generated quantitative approaches to investigate the phylogenetic distribution and function of phenotypic traits, including cognition. In particular, phylogenetic methods can quantitatively (1) test whether specific cognitive abilities are correlated with life history (e.g., lifespan), morphology (e.g., brain size), or socio-ecological variables (e.g., social system), (2) measure how strongly phylogenetic relatedness predicts the distribution of cognitive skills across species, and (3) estimate the ancestral state of a given cognitive trait using measures of cognitive performance from extant species. Phylogenetic methods can also be used to guide the selection of species comparisons that offer the strongest tests of a priori predictions of cognitive evolutionary hypotheses (i.e., phylogenetic targeting). Here, we explain how an integration of comparative psychology and evolutionary biology will answer a host of questions regarding the phylogenetic distribution and history of cognitive traits, as well as the evolutionary processes that drove their evolution.
Keywords: Biomedizin & Life Sciences
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Sigurjonsdottir, H. (2012). How does group stability and composition affect interactions in horse groups? In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Results from studies on the social behaviour of the Icelandic horse kept in different types of groups will be presented. Most groups were studied for more than 75 hours. The groups vary in composition and in stability. Some groups include stallions (6 groups) while others breeding mares and foals (1), geldings, mares, sub-adults and foals (3), geldings, sub-adults and mares (2), geldings and mares (4), one-sex 1year olds (3) and sub-adults (1). In some of the groups the residency of individual horses was similar (stable groups) while in others the composition changed frequently or unfamiliar horses were all put together at the same time. The results show that both negative and positive interactions are more frequent in unstable groups. Also, interesting differences emerged when different group types were compared. The results are important for management and will be discussed in that context. KW -
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Berger, A., & Wolfram, M. (2012). How to come together best? – Studies on integration processes of Przewalski horses into new groups (Equus ferus przewalskii). In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Conservation of endangered species in zoos and other protected areas has saved several species from extinction. The Przewalski horse (Equus ferus przewalskii) is one of that species and, being an attractive large ungulate, it is a “flagship species” for conservation projects. Reintroduction into its former habitat is accompanied by many difficulties and is a great challenge. Semireserves have been defined as enclosures large enough to maintain groups of Przewalski horses throughout all seasons of the year without any supplemental provisioning. The animals are kept isolated from external human influences as far as possible, except for necessary interventions such as veterinary care. Hence, the purpose is not limited to preparing animals for survival under natural conditions, but is equally related to the need to gain experience in establishment of free-ranging populations. Naturally, horses live in groups in which all individuals are long-term acquainted with each other and a stable hierarchical system is established. In conservation management an integration of horses into strange groups is often need but at the same time implies social fights, stress and risks for the animals. We investigated the integration process of 4 Przewalski horses from Zoo Leipzig into the herd of 5 Przewalski horses in the semireserve Liebenthal (Brandenburg, Germany). Before transportation the social structure was determined in both the herd in Zoo Leipzig and in Liebenthal. After transportation the social hierarchy and the individual dominance indices were determined by daily observation. Continuous records of activity and feeding were taken from several individuals using the ETHOSYS-storage telemetry system. The automatically recorded behaviours were analysed for daily and ultradian rhythms and used for stress detection by calculating a value (DFC) representative for regularity and stability of rhythmic structures. In zoo conditions, the behaviour was very regular and the daily pattern nearly identical from day to day as expressed by DFC´s near of 100%. After transportation, the behaviour became much less regular, DFC´s dropped significantly, recovered slowly and stabilised on values typically for semireserve conditions. Social bindings and dominances of the former two herds were mainly retained. As an important result, long lasting and stepwise transition from zoo to natural habitats with special training using new observing techniques can be strongly recommended.
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Windschnurer, I., Zeitlinger, S., Troxler, J., & Waiblinger, S. (2012). Human and horse behaviour during veterinary treatments. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Veterinary treatments are often aversive or painful, resulting in stress, avoidance, or aggressive behaviour. This preliminary study investigated which behaviours horses and humans display during veterinary examinations or treatments and if specific behaviours are shown more often during particular situations . Moreover, possible links between human and equine behaviour were investigated. Behaviours of horses, veterinarians, and assisting people were recorded at 5 clinics during 49 routine treatments that were divided into 111 situations (assigned to 7 categories: giving injections, waiting, leading horses, inspections with light body contact, invasive inspections, leg inspections, spraying/shaving). Behaviours of humans present during a situation were summarised. Behaviours (frequencies/minute) were analysed by Kruskal-Wallis tests and Spearman rank correlations. Horses showed insecurity (stopping, baulking, defecation) with different frequencies in the different categories (Chi2=23.38, df=6, P=0.001), e.g., often during leading. In humans, activating behaviour (e.g., arm waving, whistling, tongue clicking) was displayed with different frequencies (Chi2=20.42, df=6, P=0.002), e.g., frequently during leading. Restlessness in horses (e.g., stepping, head movements) tended to occur with different frequencies (Chi2=12.37, df=6, P=0.054), e.g., often during invasive inspections. Humans applied restraining techniques considered to be painful (e.g., ear twisting) with different frequencies (Chi2=26.20, df=6, P<0.001), e.g., mostly during invasive inspections. Restlessness in horses correlated with negative human interactions (e.g., hitting, talking impatiently, shouting: rs=0.28, P=0.002, n=111) and neutral human interactions (e.g., slight hits, talking dominantly: rs=0.45, P<0.001, n=111) as well as with the use of painful restraint techniques (rs=0.46, P<0.001, n=111). Moreover, avoidance behaviour of the horses (turning and stepping away) correlated with negative human interactions (rs=0.30, P=0.002, n=111). Thus, humans and horses showed certain behaviours in different situations with differing frequencies. Moreover, links between human and animal behaviour were found. Future studies should analyse causal connections, i.e., if the observed animal behaviour is the result of/or the reason for human interactions by sequence analysis. KW -
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Hillgruber, F., & Zipf, G. (2012). Humans and Horses 300.000 years ago – An approach to public presentation in the research and experience centre Schöningen spears. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: We are introducing a new research and experience center located near the stripmine of Schöningen in western Germany, one of the most important archaeological sites in the world, which is scheduled to open its doors in 2013. The 1995 discovery of wooden hunting spears (Thieme 1997) in conjunction with the remains of hunted and butchered horses (Equus mosbachensis) contributed significantly to change the scientific view of early European Hominids being “marginal scavengers” (Binford 1981, Gamble 1987) to skilled hunters. The remains of at least 19 horses were unearthed along a former lakeshore. Initial publications demonstrate early hominid butchery systematics designed to achieve a thorough acquisition of horse products (Voormolen 2008). In order to get a better understanding of the possible hunting scenario (Thieme 2007) knowledge of wild horse behaviour is of primary interest. The exhibit section of the new center is developed to present an experience oriented concept. Access to artefacts, such as the over 300.000 year old spears, is correlated with exhibits concerning Pleistocene horse morphology, group structure and behaviour of modern day wild horses in order to draw a vivid image of the past
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Mshelia, W. P., Abdussamad, A. M., Onoja, I. I., Victoria, S.Q., & Richard, E. E. (2012). Husbandry and Management Practices in Domestic horses in Northern Nigeria and their Clinical Implications. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: This study was conducted to identify common husbandry and management practices associated with domestic horses in Northern Nigeria. Fifty (50) of the horse was purposely selected as units of analysis. Primary data was generated by means of a pre-tested, semi-structured questionnaire administered to the sampled respondents. A simple inductive statistics was applied to the primary data. The study revealed that the whole facilities studied 50(100%) had a prior experience with horses. A large number of horses, mostly West African Dongola and West African Barb are kept solely for pleasure or ceremonial purposes (60%). While the other breeds of horses like Argentine (6%) and South Africa polo ponies (2%) are kept for polo. Recently, the Sudan country-bred (4%) and Western Sudan pony (6%) have found a place in West African polo. Other breeds found within the facilities studied are Argentine criollo; Nigerian ponies and various crosses. Only 10% of the facilities had breeding stocks with only 2% carrying out artificial insemination while 8% do natural mating. The housing management system includes stables (40%) and open fields (60%) where horses are tethered. Bedding materials includes straws (50%); sand (20%) and wood shavings (30%). Feed grade provided include a combination of rations-bran; cracked grain and hay (40%), Bran; cracked grain and legumes (48%) and Bran and hay (12%), all feed combination administered along with fresh grass. Watering and feeding practices involves provision of feed and water twice daily (50%) and while others provide it adlib (25%). Feeding horses with various additives accounted for 19% of the studied facilities. The health status as shown by the body condition score ranges from II-IV/V (88%) of the population studied. Routine dental care is regular (30%) with all the facilities while others (70%) are not irregular. Grooming is common in all the facilities especially within the performance horse circle. Routine hoof care including trimming and shoeing is common in 26% of the facilities while hoof trimming without shoeing is a common practice in 74% of the facilities. Orthodox medicine practiced in 80% of the studied area. While ethnoveterinary consist of 10%, while a combination of orthodox and ethnoveterinary medicine was common in 10% of the study area. Vaccination against African horse sickness equine influenza and tetanus is common in the various equine communities.Though 16% of the population do not vaccinate against any known disease. Parasite control program include pasture hygiene (4%); interval dosing (10%); continuous in-feed (4%); selective dosing (40%) and strategic dosing constitute 42%. Exercise is a common practice but intensity and duration is not strictly adhered to especially during tendon injuries. Manure management differs from facility to facility- some dispose manure within the facilities (40%) while others dispose it outside the facilities (60%). A number of clinical signs like limping, coughing, ocular and nasal discharge, swellings on the body, abnormal mucous membrane, fever, ventral oedema and reluctance to move, foul respiratory odour was observed. Clinical cases like laminitis; pigeon fever; bran disease; colic; African horse sickness; exertional rhabdomyolysis; sinusitis; piroplasmosis; dermatomycosis and tumours was observed. KW -
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Wulf, M., Aurich, C., Nees, M., & Aurich, J. (2012). Identification of horses – hot iron branding versus microchip transponders. In K. Krueger (Ed.), Proceedings of the 2. International Equine Science Meeting (Vol. in press). Wald: Xenophon Publishing.
Abstract: Identification of horses with hot iron branding is one of the most controversial issues in German horse breeding and also discussed in other countries. Traditionally horses have been identified by hot iron branding with breed-specific symbols and additional numbers. Since 2009, European Union legislation requires that all horses born after that year must have a microchip implanted for identification, although some exceptions are possible. So far it has not been tested using scientific criteria to what extent branding and microchips reliably allow identification of individual horses. In this study, the readability of branding symbols and numbers was analyzed by 3 independent investigators in 248 horses participating in an equestrian competition. Microchip transponders implanted into the neck were read in another 182 horses on different breeding farms. Microchip readings were made on both sides of the neck and 3 different commercially available ISO 11785/11785 scanners were compared (A: Minimax II, B: I-MaxPlus, C: Isomax V, all by Virbac, Germany). Correct reading of the branding breed symbol in horses at an equestrian championship by the individual investigators was close to 90% and differed only marginally between the investigators. Correct identification of the breed-specific symbol by all 3 investigators occurred in 84% of cases. The double-digit number branded together with the breed symbol was identified correctly by all 3 investigators in 39% of cases with correct readings by individual investigators ranging from 47 to 54%. Correct identification of the branding signs did not differ significantly between horses of different coat color and age group. Readability of microchips differed between scanners. Best results were obtained with scanner C which allowed microchip reading on the implantation side in 100% and on the contralateral side of the neck in 95% of 182 horses. Time for location of the microchip on the implanted side ranged from 1 to 4 sec (1.1±0.4). Scanner A identified 92 and 25% of microchips on the implanted and contralateral side, respectively while corresponding values for scanner B were 86 and 20%. Readability of microchip transponders on the side contralateral to implantation was influenced by size and thus caliber of the horse. In conclusion, hot iron branding does not allow unique identification of horses and individual branding numbers can be read in less than 40% of the horses. Readability of microchip transponders is more reliable compared to hot iron branding but depends on the type of scanner used. Scanner C allowed identification of all horses tested and gave good results also when used on the contralateral side of the horses` neck. KW -
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Hartmann, E., Søndergaard, E., & Keeling, L. J. (2012). Identifying potential risk situations for humans when removing horses from groups. Appl. Anim. Behav. Sci., 136(1), 37–43.
Abstract: Removing a horse from its social group may be considered risky, both for the handler and the horse, because other horses can interfere in the catching process. The main aim of this study was to identify where and when these risk situations occur while removing a horse from its group. A potential risk situation was defined by the closeness of loose horses in the group or by any physical contact with them. Whether the number of horses following would be influenced by the social rank of the horse being led out, and whether more horses would follow to the gate when a larger proportion of the group was removed compared to when a single horse was taken out were also investigated. Thirty-two mares (1–2 years) were kept in groups of four. All horses were taken out of their home paddock twice alone (64 tests) and twice with a companion (32 tests). One handler (or two handlers when two horses were removed) was asked to approach (phase 1) and catch the target horse (phase 2), walk it to the centre of the paddock and remain stationary at a post for 30 s (phase 3), walk to the paddock entrance (phase 4) and through the gate (phase 5). The number of horses following, and the number of loose horses in proximity (<2 m, 2–5 m) to the target horse and handler was estimated, and horse–horse and horse–human interactions were recorded continuously for the five scoring phases. Significantly more loose horses were within 2 m of a single target horse during the phases approach (mean ± SD: 1.5 ± 0.8), catch (1.6 ± 0.9) and post (1.7 ± 0.7) than during walk (1.0 ± 0.5) and gate (1.1 ± 0.6). Rank did not influence the number of horses following to the gate (high rank: 2.4 ± 0.7; lower rank: 2.0 ± 1.0; P = 0.396) and interactions between horses were rare. A greater proportion of the loose horses followed when two horses (0.9 ± 0.2) were removed compared to when a single horse (0.7 ± 0.3) was taken out (P = 0.011). In conclusion, maintaining a distance to other horses in the group by reducing the time being relatively stationary, so giving loose horses fewer chances to approach, is likely to contribute to improved handler's safety. Removing a small proportion of the group may also decrease the probability of the other horses following.
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