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Warmuth, V.; Eriksson, A.; Bower, M.A.; Barker, G.; Barrett, E.; Hanks, B.K.; Li, S.; Lomitashvili, D.; Ochir-Goryaeva, M.; Sizonov, G.V.; Soyonov, V.; Manica, A. |
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Title |
Reconstructing the origin and spread of horse domestication in the Eurasian steppe |
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Journal Article |
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2012 |
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Proceedings of the National Academy of Sciences |
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Proc Natl Acad Sci U S A |
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Despite decades of research across multiple disciplines, the early history of horse domestication remains poorly understood. On the basis of current evidence from archaeology, mitochondrial DNA, and Y-chromosomal sequencing, a number of different domestication scenarios have been proposed, ranging from the spread of domestic horses out of a restricted primary area of domestication to the domestication of numerous distinct wild horse populations. In this paper, we reconstruct both the population genetic structure of the extinct wild progenitor of domestic horses, Equus ferus, and the origin and spread of horse domestication in the Eurasian steppes by fitting a spatially explicit stepping-stone model to genotype data from >300 horses sampled across northern Eurasia. We find strong evidence for an expansion of E. ferus out of eastern Eurasia about 160 kya, likely reflecting the colonization of Eurasia by this species. Our best-fitting scenario further suggests that horse domestication originated in the western part of the Eurasian steppe and that domestic herds were repeatedly restocked with local wild horses as they spread out of this area. By showing that horse domestication was initiated in the western Eurasian steppe and that the spread of domestic herds across Eurasia involved extensive introgression from the wild, the scenario of horse domestication proposed here unites evidence from archaeology, mitochondrial DNA, and Y-chromosomal DNA. |
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Equine Behaviour @ team @ |
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5612 |
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Kaminski, G.; Gentaz, E.; Mazens, K. |
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Title |
Development of children’s ability to detect kinship through facial resemblance |
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2012 |
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Animal Cognition |
Abbreviated Journal |
Anim. Cogn. |
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15 |
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3 |
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421-427 |
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Biomedizin & Life Sciences |
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Facial features appear to be a prominent kinship cue for ascribing relatedness among human individuals. Although there is evidence that adults can detect kinship in unrelated and unfamiliar individual’s faces, it remains to be seen whether people already possess the ability when they are young. To further understand the development of this skill, we explored children’s ability to detect parent-offspring resemblance in unrelated and unfamiliar faces. To this end, we tested approximately 140 children, aged 5–11, in two photo-matching tasks. We used a procedure that asked them to match one neonate’s face to one of three adults’ faces (Task 1), or to match one adult’s face to one of three neonate’s faces (Task 2). Our findings reveal asymmetrical performance, depending on the tasks assigned (performance of Task 2 is stronger than for Task 1), and on the sex of individuals who made up the parent-offspring pair (male parents are better matched with neonates than female parents, and boys are better matched than girls). The picture that emerges from our study is, on one hand, that the ability to detect kinship is already present at the age of five but continues to improve as one gets older, and on the other, that perception of parent-offspring facial resemblance varies according to the appraisers’ characteristics. |
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Springer Berlin / Heidelberg |
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Equine Behaviour @ team @ |
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5605 |
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MacLean, E.; Matthews, L.; Hare, B.; Nunn, C.; Anderson, R.; Aureli, F.; Brannon, E.; Call, J.; Drea, C.; Emery, N.; Haun, D.; Herrmann, E.; Jacobs, L.; Platt, M.; Rosati, A.; Sandel, A.; Schroepfer, K.; Seed, A.; Tan, J.; van Schaik, C.; Wobber, V. |
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How does cognition evolve? Phylogenetic comparative psychology |
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Journal Article |
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2012 |
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Animal Cognition |
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Anim. Cogn. |
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15 |
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2 |
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223-238 |
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Biomedizin & Life Sciences |
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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. |
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Springer Berlin / Heidelberg |
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1435-9448 |
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Equine Behaviour @ team @ |
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5604 |
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Van de Weerd, H.A.; Seaman, S.; Wheeler, K.; Goddard, P.; Mclean, B. |
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Title |
Use of artificial drinkers by unhandled semi-feral ponies |
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Journal Article |
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2012 |
Publication |
Applied Animal Behaviour Science |
Abbreviated Journal |
Appl. Anim. Behav. Sci. |
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139 |
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1-2 |
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86-95 |
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Semi-feral Dartmoor ponies; Drinking behaviour; Preference tests; Welfare |
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This study investigated drinking behaviour of unhandled, semi-feral Dartmoor ponies. Aspects studied were drinking behaviour, latency to drink from novel unfamiliar drinkers after transport, preferences for different types of artificial water drinkers, effects of mixing with unfamiliar ponies and group size, on drinking behaviour, and the effect of a simulated market on the latency to drink. Ponies were tested in groups of three or six animals, or as individuals in test pens that were equipped with three water drinkers: bucket, automatic drinking bowl, flowing water trough. Behaviour was recorded using time-lapse video. An individual pony drank on average 10 l per day. Ponies also drank, but at a lower rate, during the night. The latencies to drink after 4.5 h of transport showed large variation, but most ponies drank within the first hour after being transported (all groups 80.5 ± 32.94 min, mean ± SEM). In the individual choice tests, the preferred drinkers were the bucket and the flowing water trough, but not the automatic drinking bowl (drinking time 25.2 ± 4.66, 11.5 ± 4.26, 2.4 ± 2.23 min for bucket, trough and bowl respectively, mean ± SEM; paired t-tests, bowl versus other drinkers, all tests p < 0.02). A possible reason for the avoidance of the automatic bowl was the noise it made when filling. After mixing a group of three ponies with a group of three unfamiliar animals, the ponies did not express their individual drinker preferences anymore. The use of the previously preferred bucket decreased significantly and the use of the initially, non-preferred, bowl increased significantly. This was likely caused by the fact that ponies were either intentionally or accidentally obstructing drinkers in certain areas of the pen and unfamiliar ponies did not want to push past them. In the simulated market, the differences in latencies to drink between ponies in the home pen and market groups did not reach significance. No significant effect of group size (groups of three versus six ponies) on drinking behaviour was detected. The results have implications for situations where only automatic water bowls are provided, such as during pony sales at livestock markets. Preventing ponies from expressing their drinking choice, either by offering non-preferred drinkers or by mixing with unfamiliar animals, could adversely affect their welfare especially if this happens in conjunction with other stressful events such as transport and markets, and potentially weaning. |
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0168-1591 |
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Equine Behaviour @ team @ |
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5596 |
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Dumont, B.; Rossignol, N.; Loucougaray, G.; Carrère, P.; Chadoeuf, J.; Fleurance, G.; Bonis, A.; Farruggia, A.; Gaucherand, S.; Ginane, C.; Louault, F.; Marion, B.; Mesléard, F.; Yavercovski, N. |
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When does grazing generate stable vegetation patterns in temperate pastures? |
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2012 |
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Agriculture, Ecosystems & Environment |
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153 |
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50-56 |
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Boolean process; Cattle; Patch stability; Productivity; Stocking density; Temperate pasture |
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The stability of grazing-induced spatial patterns of vegetation was analyzed at two spatial scales (25 m × 20 m areas and 1.6 m × 0.8 m grids) in pastures of contrasting productivity (maximum standing biomass: 130–800 gDM/m2). At both scales, the mosaic of grazed and ungrazed patches was modeled as a Boolean process, calculating cross-variograms to quantify the temporal stability of grazing patterns and its links with local floristic composition were tested. The scale at which stability of vegetation patterns took place in two successive years depended on pasture productivity. Inter-annual stability of large-scale patterns mainly occurred in extensively used fertile pastures grazed by cattle, and in pastures grazed by horses. Less-fertile grasslands were mainly characterized by a fine-scale stability of grazing patterns. Stable fine-scale patterns were often related to the local abundance of legumes and forbs. Stable large-scale patterns of grazing within lightly grazed productive grasslands could result in divergent local vegetation dynamics, which can be seen as an opportunity for restoring biodiversity in fertile grasslands. |
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0167-8809 |
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Equine Behaviour @ team @ |
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5595 |
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Szarka, A.; Nagy, K.; Maros, K. |
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Approaching a horse, approaching a human: Tolerating and seeking human contact in pastured horses |
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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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We tested untrained horses (foals and breeding mares) in 3 different breeding centres. Horses were kept in a pasture during daytime in bigger groups (median 12, min: 6, max 35 / pasture) according to age, gender and breed (hungarian halfbred, hucul, arabian and thoroughbred). To measure their reactions to an unfamiliar person we conducted an active and a passive human test. In the active human test the test person (TP) approached a focal animal in the group from a predetermined direction: from their front, from their side (left or right) or from the rear. As TP reached the horse (of app. 0.5 m distance), she tried to pet the animal’s head. The TP always chose and approached a standing or a grazing horse (ie. those that were not walking, galloping, playing etc.). The horse’s reaction to the approaching human was scored 1-5. Score 1: the horse moved away and the TP could not even approach it within 0.5 m; Score 2: the horse made max. 2 steps away, but could be reached and petted; Score 3 and Score 4: the horse stood in its place but showed different signs of discomfort (head turn – Score 3; backing ears, tail slash – Score 4); Score 5: the horse stood and did not show any sign of discomfort or actively approached the TP. There was no significant difference in the horses’ reaction between approaching from their left or right side. Approaching from their front or from their side (left or right) did not differ significantly either. However, the odds of walking away from the TP (score 1 or 2) was 2.7 (Fisher-test, p=0.039) and 3.3 (p=0.012) times higher when TP approached from the rear compared to approaching from their front or from their side (left or right), respectively. In the passive human test the TP stood immobile for 4 minutes in 5 or 10 m far from the horses during their active (grazing) or inactive (standing idle during noon) period. Horses approached TP significantly sooner (general linear model, p=0.017) when she stood 5m distance (38 ±63 s) compared to 10m (97 ±52 s). The arrival of a second horse after the first horse approached the TP showed significant high correlation with the latency of the first horse arrival (Pearson correlation, r=0.96, p<0.001). The horses were less keen (p=0.008) to approach the human when they were tested in an inactive period (177 ±110 s) compare to active period (38 ±63 s). |
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Maros, K. |
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Xenophon Publishing |
Place of Publication |
Wald |
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Krueger, K.; |
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978-3-9808134-26 |
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Equine Behaviour @ team @ |
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5594 |
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Author |
Lancet, Y.; Dukas, R. |
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Title |
Socially Influenced Behaviour and Learning in Locusts |
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Journal Article |
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Year |
2012 |
Publication |
Ethology |
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118 |
Issue |
3 |
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302-310 |
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As a part of our research on the evolution of social learning in insects, we examined socially influenced behaviour and social learning in desert locust (Schistocerca gregaria) nymphs and adults. In the nymphs, the only positive effect we documented was an increased tendency to feed while in the company of another locust than alone. The adults, on the other hand, showed significant preference for joining others (local enhancement) in both the contexts of feeding and egg laying. Neither nymphs nor adults, however, showed social learning. Our preliminary analyses pointed to locusts as a likely insect that might possess social learning. Our research, when taken together with research on phase-shifts and swarm/marching behaviour of gregarious locusts, suggests that the behavioural dynamics of gregarious locusts may make local enhancement but not social learning beneficial. The possible difference we documented between the nymphs and adults could enable us to further explore the proximate and ultimate mechanisms that underlie socially influenced behaviour. |
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Blackwell Publishing Ltd |
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1439-0310 |
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Equine Behaviour @ team @ |
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5593 |
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Bouskila, A.; de Vries, H.; Hermans, Z.M.; van Dierendonck, M. |
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Title |
Leadership roles in movements of free-roaming Konik horses (Equus caballus) in a Dutch reserve |
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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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We observed the activity and movements of Konik horses (Equus caballus) in order to determine the initiators of movements and the individuals taking the lead in movements of the main groups. We conducted our observations between March-June 2010 along the shores of the Rhine river, in the Blauwe Kamer reserve, in the Netherlands. The horses were introduced to the reserve alongside with cattle to prevent the growth of the forest and maintain the grass habitat. We videotaped all observations on two digital video cameras, one providing the general view of the group and the other scanning and focusing on the individuals, to aid with identification. Horses were recognized based on individual profiles that were created for each one, consisting of photos of both sides and notes of the main characters, such as orientation and coloration of the mane, prominent scars and markings, etc. Twenty three horses (not counting foals) were organized in two harem groups with 11 individuals (two of which were dominant stallions) in the large group and six individuals (one of which was a stallion) in the second group. These two main groups were always within sight of each other, and two bachelor males moved usually in their vicinity. An additional group of three young bachelor males roamed elsewhere in the reserve. We divided the movements of the horses to local movements while grazing and to long-distance movements, in which the horses moved to a different grazing location, to a pond of water, resting area or groups of trees that were used by the horses for scratching themselves. During the local movements, any two of the three oldest females in the large harem group were enough to cause the whole group to follow them and gradually change position within the pasture. The smaller harem always followed the large harem’s movements. The long-distance movements of the large harem were sometimes initiated by one of the harem stallions that herded their group and at other times – by the oldest females. Soon after the movement was clearly initiated, the dominant stallions positioned themselves in the back of the group or in the center and had no influence on the direction of move that was only determined by the leading females. In the long-distance movements too, the small harem followed the large harem group, and the two bachelor males usually followed behind them. Social interactions included aggressive interactions between the two dominant males within the large harem or between dominant stallions and the two bachelor males accompanying the two harems. In addition, dominant males courting or attempting to mate with mares sometimes caused a turmoil that eventually initiated movement of the harems. KW - |
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Corporate Author |
Bouskila, A. |
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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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5592 |
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Author |
Flauger, B.; Krueger, K. |
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Title |
Social feeding decisions in horses (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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Feeding decision; Horse; Rank; Social behaviour |
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Like many other herbivores equids feed on rather evenly distributed resources. Especially in ruminants several studies have proved the influence of social organisations, rank, sex and the depletion of feeding sites on the feeding behaviour of individuals. However, it is not yet understood whether social aspects affect horses´ feeding decisions. Horses roam on vast habitats with constantly changing vegetation. In non-competitive situations domestic horses tend to return to the same feeding site until it is overgrazed. Whereas, for competition over limited food the social status of the individuals appears to be important. Curiosity about the influence of social rank and different social feeding conditions on the horses´ feeding decisions between two buckets, equally filled with high-quality surplus food, led us to create the test situation described here. The observer horses were alternately tested with a dominant and a subordinate demonstrator placed in one of three different positions. We conclude that domestic horses use cognitive strategic decision making in order to decide where to feed in a social feeding situation. When possible they tend to return to the same, continuously supplied feeding site and switch to an “avoidance tendency” when another horse is already feeding from it or in the presence of a dominant horse. Thus the position and the social rank of conspecifics affect the feeding strategy of horses. |
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Corporate Author |
Flauger, B. |
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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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5581 |
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Author |
Ermilina, J.A. |
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Title |
Dominance hierarchy in feral horses in Rostov Region |
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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Keywords |
feral horse, island population, dominance, hierarchy |
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Abstract |
Horses maintain the social structure through the establishment of dominant-subordinate hierarchical relationships, both within and between groups. The object of study was the feral horse population, living on the Vodnyi Isl, Manych-Ghudilo Lake, on the territory of Rostov Region, S Russia the State Nature Biosphere Reserve “Rostov”. The social structure of this population is represented by the harem and bachelor groups, and their variety – the “mixed”groups, the presence and composition of which is atypical for the populations of feral horses. The main objectives of this work were to identify the hierarchical structure of different types of social groups and the role of the stallions in them, defining the dominance rank of animals. The method of continuous logging occurred aggressive reaction, ritualized interaction between stallions, take into account the direction of interactions between individuals. We observed 5 harem, 3 bachelor and 3 mixed groups. Each group was studied for a total of 60 h (8 h per group per days).Behavioral observations were carried out in summer 2009-2011. Based on the number and direction of aggressive interactions the hierarchical coefficient was calculated for individual horses (Ivanov et al, 2007). Harem group consists of an adult stallion (<5 years old) and a few mares with their offspring. Our observations of harem groups confirm the previously known information about this type of social groups (Berger, 1986; Carson, Wood-Gush, 1983, Keiper, 1983). Hierarchical system between mares is close to linear with reversal. The stallion is not included in the hierarchy of the mares; he is the leader and serves to maintain the integrity of the group and inter-group hierarchy, and has reproductive function. Bachelor groups consist of stallions 2-3 years and older who do not have their own harem. It is known that dominance hierarchy in these groups is linear, young males or males who recently had joined the group have low ranks (Berger, 1977; Houpt, Keiper, 1982; Kirillov Paklina, 1990). In observed bachelor groups dominant stallion have a significantly higher rank in the hierarchy. However, among other stallions is not always observed strict linear hierarchy – some individuals have very similar ranks. Function of managing the group and maintaining the intergroup hierarchy can be distributed among the all stallions in the group. Mixed groups are composed of several mature stallions, one or more mares (sometimes with the offspring). In the study population in this type of social groups animals may be mature (age 5 and older) and semi-mature (2-5 years). The hierarchy of these atypical groups has not been studied. In the studied 3 mixed groups stallions have very similar hierarchical rank, dominant and subordinate stallions share a function of managing the group, participation in ritualized interactions. Our studies have revealed the plasticity of the hierarchical structure of groups of horses and the need to further investigate the distribution of social roles among stallions. |
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Ermilina, J.A. |
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Xenophon Publishing |
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Wald |
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Krueger, K.; |
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978-3-9808134-26 |
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Equine Behaviour @ team @ |
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5580 |
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