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Capitani, C.; Chynoweth, M.; Kusak, J.; Çoban, E.; Sekercioglu, Ç.H. |
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Title |
Wolf diet in an agricultural landscape of north-eastern Turkey |
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Journal Article |
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2016 |
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Mammalia |
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Mammalia |
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80 |
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3 |
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329-334 |
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Mammalia |
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80 |
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3 |
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Equine Behaviour @ team @ |
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6687 |
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Author |
Iliopoulos, Y.; Sgardelis, S.; Koutis, V.; Savaris, D. |
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Title |
Wolf depredation on livestock in central Greece |
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Journal Article |
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Year |
2009 |
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Mammal Research |
Abbreviated Journal |
Mamm. Reas. |
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54 |
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1 |
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11-22 |
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We studied wolfCanis lupus Linnaeus, 1758 -- livestock conflict in central Greece by investigating patterns of 267 verified wolf attacks on livestock for 21 months. Wolves attacked adult goats 43% and cattle 218% more than expected, whereas sheep 41% less than expected from their availability. Wolves killed less than four sheep or goats in 79%, and one cow or calf in 74% of depredation events, respectively. We recorded higher attack rates during wolf post-weaning season. Wolf attacks on strayed, or kept inside non predator-proof enclosures, sheep and goats, were on average two to four times respectively more destructive than those when livestock was guarded by a shepherd. Sheepdog use reduced losses per attack. Optimal sheepdog number ranged from 3 to 9 animals depending on flock size. Losses per attack were positively related to the number of wolves involved. Total losses per farm were positively correlated with the size of livestock unit but percentage losses per capita increased with decreasing flock size. Management implications to mitigate livestock depredation are discussed. |
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2199-241x |
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Equine Behaviour @ team @ Iliopoulos2009 |
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6576 |
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Author |
Myslajek, R.W.; Tracz, M.; Tracz, M.; Tomczak, P.; Szewczyk, M.; Niedzwiecka, N.; Nowak, S. |
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Title |
Spatial organization in wolves Canis lupus recolonizing north-west Poland: Large territories at low population density |
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Journal Article |
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Year |
2018 |
Publication |
Mammalian Biology |
Abbreviated Journal |
Mamm. Biol. |
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92 |
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37-44 |
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Wolf recovery; Spatial organization; GPS/GSM telemetry; Central European wolf population |
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Monitoring of the wolf Canis lupus is a demanding task as it lives in low densities, utilizes vast home ranges and disperses over large areas. These factors make obtaining accurate data about population parameters over the whole distribution area of the species impossible. Thus detailed local studies on socio-spatial organization are essential to calibrate information obtained over a larger area. We applied GPS/GSM telemetry, non-invasive genetic sampling, year-round tracking, camera trapping and howling stimulations to determine the number of family groups, population density and home-range sizes of wolves in the Drawa Forest (DF, western Poland, 2500 km2), an area recently recolonized by the species. Home ranges of three collared male wolves ranged from 321.8 to 420.6 km2 (MCP 100%) and from 187.5 to 277.5 km2 (Kernel 95%), but core areas had a size of 30.5-84.7 km2 (MCP50%) and 35.0-88.8 km2 (Kernel 50%). Mean near neighbour distance between centres of 6 tracked pack homesites was 15.3 km. The number of wolves in DF increased from 14 individuals in 2013/2014 to 30 in 2016/2017. The annual rate of increase varied from 43% in 2014/2015 to 7% in the final year. Population density for the whole study area was relatively low (1.2 indiv./100 km2 in 2016/2017), but densities within territories of two packs studied with telemetry were 1.9 and 1.5 indiv./100 km2. Mean pack size varied between 3.5 and 5.6 individuals, with the largest pack comprising 8 wolves. Mean number of pups observed in summers (June-August) was 4.5. Differences in home range sizes between wolves in western and eastern Poland indicate that results of regional studies cannot be freely extrapolated despite close genetic relationships. Thus, decisions related to management of wolf habitats should be based on intensive local studies. |
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1616-5047 |
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Equine Behaviour @ team @ |
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6503 |
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Author |
Kruska, D.C.T. |
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Comparative quantitative investigations on brains of wild cavies (Cavia aperea) and guinea pigs (Cavia aperea f. porcellus). A contribution to size changes of CNS structures due to domestication |
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Journal Article |
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Year |
2014 |
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Mammalian Biology – Zeitschrift für Säugetierkunde |
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Mamm Biol |
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79 |
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4 |
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230-239 |
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Domestication; Allometry; Brain structure volumes; Brain-behavior correlation |
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Intraspecific allometric calculations of the brain to body size relation revealed distinct differences between 127 (67; 60) ancestral wild cavies and 82 (37; 45) guinea pigs, their domesticated relatives. The dependency of both measures from one another remained the same in both animal groups but the brains of guinea pigs were by 14.22% smaller at any net body weight. Consistent with results in other species the domestication of Cavia aperea is also characterized by a decrease of brain size. Fresh tissue sizes of the five brain parts medulla oblongata, cerebellum, mesencephalon, diencephalon and telencephalon were determined for 6 cavies and 6 guinea pigs by the serial section method. Additionally the sizes of 16 endbrain structures and those of the optic tract, the lateral geniculate body and the cochlear nucleus were measured. Different decrease values resulted for all these structures concomitant with domestication as was calculated from the amount of total brain size decrease and average relative structure values in the wild as well as the domesticated brain. The size decrease of the entire telencephalon (-13.7%) was within the range of the mean overall reduction as similarly was the case for the total neocortex (-10.7%) whereas the total allocortex (-20.9%) clearly was more strongly affected. The size decrease of the olfactory bulb (-41.9%) was extreme and clearly higher than found for the secondary olfactory structures (around -11%). The primary nuclei of other sensory systems (vision, audition) were decreased to less extent (lateral geniculate: -18.1%; cochlear nucleus: -12.6%). Mass decreases of pure white matter parts were nearly twice as high in contrast to associated grey matter parts (neocortex white versus grey matter; tractus opticus versus lateral geniculate body). The relatively great decrease values found for the limbic structures hippocampus (-26.9%) and schizocortex (-25.9%) are especially notable since they are in good conformity with domestication effects in other mammalian species. The findings of this study are discussed with regard to results of similar investigations on wild and domesticated gerbils (Meriones unguiculatus), the encephalization of the wild form, the special and species-specific mode and duration of domestication and in connection with certain behavioral changes as resulted from comparative investigations in ethology, socio-biology, endocrinology and general physiology. |
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Admin @ knut @ |
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6401 |
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Cooper, J.J.; Albentosa, M.J. |
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Behavioural adaptation in the domestic horse: potential role of apparently abnormal responses including stereotypic behaviour |
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Journal Article |
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Year |
2005 |
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Livestock Production Science |
Abbreviated Journal |
Livest. Prod. Sci. |
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92 |
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2 |
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177-182 |
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Behavioural adaptation; Horse; Stereotypic behaviour |
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Classically, biologists have considered adaptation of behavioural characteristics in terms of long-term functional benefits to the individual, such as survival or reproductive fitness. In captive species, including the domestic horse, this level of explanation is limited, as for the most part, horses are housed in conditions that differ markedly from those in which they evolved. In addition, an individual horse's reproductive fitness is largely determined by man rather than its own behavioural strategies. Perhaps for reasons of this kind, explanations of behavioural adaptation to environmental challenges by domestic animals, including the capacity to learn new responses to these challenges, tend to concentrate on the proximate causes of behaviour. However, understanding the original function of these adaptive responses can help us explain why animals perform apparently novel or functionless activities in certain housing conditions and may help us to appreciate what the animal welfare implications might be. This paper reviews the behavioural adaptation of the domestic horse to captivity and discusses how apparently abnormal behaviour may not only provide a useful practical indicator of specific environmental deficiencies but may also serve the animal as an adaptive response to these deficiencies in an “abnormal” environment. |
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0301-6226 |
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Equine Behaviour @ team @ |
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4829 |
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Whiten, A.; Horner, V.; Litchfield, C.A.; Marshall-Pescini, S. |
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How do apes ape? |
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Journal Article |
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2004 |
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Learning & Behavior |
Abbreviated Journal |
Learn. Behav. |
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32 |
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1 |
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36-52 |
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Adaptation, Psychological; Animals; Behavior, Animal; Hominidae/*psychology; *Imitative Behavior; Imprinting (Psychology); *Learning; Psychological Theory; *Social Environment; *Social Facilitation |
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In the wake of telling critiques of the foundations on which earlier conclusions were based, the last 15 years have witnessed a renaissance in the study of social learning in apes. As a result, we are able to review 31 experimental studies from this period in which social learning in chimpanzees, gorillas, and orangutans has been investigated. The principal question framed at the beginning of this era, Do apes ape? has been answered in the affirmative, at least in certain conditions. The more interesting question now is, thus, How do apes ape? Answering this question has engendered richer taxonomies of the range of social-learning processes at work and new methodologies to uncover them. Together, these studies suggest that apes ape by employing a portfolio of alternative social-learning processes in flexibly adaptive ways, in conjunction with nonsocial learning. We conclude by sketching the kind of decision tree that appears to underlie the deployment of these alternatives. |
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Centre for Social Learning and Cognitive Evolution, Scottish Primate Research Group, School of Psychology, University of St. Andrews, St. Andrews, Fife, Scotland. a.whiten@st-and.ac.uk |
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English |
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1543-4494 |
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PMID:15161139 |
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no |
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refbase @ user @ |
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734 |
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Author |
Laland K.N. |
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Title |
Social learning strategies |
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Journal Article |
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2004 |
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Learning & Behavior |
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Learn. Behav. |
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32 |
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4-14 |
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In most studies of social learning in animals, no attempt has been made to examine the nature of the strategy adopted by animals when they copy others. Researchers have expended considerable effort in exploring the psychological processes that underlie social learning and amassed extensive data banks recording purported social learning in the field, but the contexts under which animals copy others remain unexplored. Yet, theoretical models used to investigate the adaptive advantages of social learning lead to the conclusion that social learning cannot be indiscriminate and that individuals should adopt strategies that dictate the circumstances under which they copy others and from whom they learn. In this article, I discuss a number of possible strategies that are predicted by theoretical analyses, including copy when uncertain, copy the majority, and copy if better, and consider the empirical evidence in support of each, drawing from both the animal and human social learning literature. Reliance on social learning strategies may be organized hierarchically, their being employed by animals when unlearned and asocially learned strategies prove ineffective but before animals take recourse in innovation. |
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Equine Behaviour @ team @ |
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4193 |
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Author |
Siniscalchi, M.; Padalino, B.; Aubé, L.; Quaranta, A. |
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Title |
Right-nostril use during sniffing at arousing stimuli produces higher cardiac activity in jumper horses |
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Journal Article |
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2015 |
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Laterality: Asymmetries of Body, Brain and Cognition |
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Laterality |
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20 |
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4 |
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483-500 |
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Lateralization in horses, Equus caballus, has been reported at both motor and sensory levels. Here we investigated left- and right-nostril use in 12 jumper horses freely sniffing different emotive stimuli. Results revealed that during sniffing at adrenaline and oestrus mare urine stimuli, horses showed a clear right-nostril bias while just a tendency in the use of the right nostril was observed during sniffing of other odours (food, cotton swab and repellent). Sniffing at adrenaline and urine odours was also accompanied by increasing cardiac activity and behavioural reactivity strengthening the role of the right hemisphere in the analysis of intense emotion and sexual behaviour. |
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Routledge |
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1357-650x |
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doi: 10.1080/1357650X.2015.1005629 |
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Equine Behaviour @ team @ |
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6208 |
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Author |
Osman, F.; Zeitler-Feicht, M.; Fink, G. W.; Arnhard, S.; Krüger, K. |
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Überprüfung der lichten Weiten von Gitterstäben in der Pferdehaltung [Analysing demands for the clear widths of lattice bars in horse husbandry] |
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Journal Article |
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2020 |
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Landtechnik [Agricultural Engineering] |
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75 |
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1 |
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24-33 |
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An Gitterstäben, die in der Pferdehaltung an verschiedenen Stellen verwendet werden, können sich Pferde verletzen, wenn sie ihre Köpfe oder ihre Hufe hindurchstecken und nicht zurückziehen können. Um das Verletzungsrisiko zu reduzieren sind lichte Weiten und Materialstärken von Gitterstäben so zu wählen, dass Pferdeköpfe und -hufe entweder nicht zwischen den Freiräumen hindurchpassen oder aber gefahrlos wieder zurückgezogen werden können. Die bisherige Forschung liefert jedoch keine belastbaren Aussagen zu Stababständen (senkrecht und waagerecht), die für Pferde ungefährlich sind. Die in der Praxis verwendeten und in der Literatur empfohlenen Gitterstababstände beruhen auf Erfahrungswerten und technischen Materialeigenschaften. In der vorliegenden Untersuchung wurden Pferdeköpfe und -hufe von insgesamt 480 Pferden (233 Stuten, 204 Wallache und 43 Hengste) von 23 verschiedenen Rassen vermessen, um auf Grundlage der Anatomie der Pferde Aussagen über die Eignung von marktüblichen Stababständen in der Praxis treffen zu können. Es stellte sich heraus, dass bei senkrechten Gitterstäben eine lichte Weite von nicht mehr als 5 cm für alle Pferde ab einem Stockmaß von 110 cm und einem Alter von zwei Jahren als sicher bezeichnet werden kann. Bei waagerechten Gitterstäben erwies sich eine lichte Weite von genau 17 cm als sicher. Dies gilt für alle Pferde ab einem Alter von zwei Jahren oder ab einem Stockmaß von 148 cm.
Kritisch sind die lichten Weiten von Panels zu beurteilen. Hier zeigte sich, dass die handelsüblichen Abstände der Gitterstäbe für die meisten Pferde eine erhebliche Gefahr darstellen. Wenn die Pferde beispielsweise versuchen außerhalb der Panels zu fressen und dabei ihren Kopf durch die Gitterstäbe stecken, kann es leicht passieren, dass sie sich mit dem Kopf zwischen den Gitterstäben verklemmen.
[At bars, used in various places in horse husbandry, horses can hurt themselves when retracting their heads or hooves after pushing them through the interspaces. In order to reduce the risk of injury, the clear widths and material thicknesses of bars should be chosen so that horse heads and hooves either cannot pass between the spaces or can be retracted safely. However, research to date has not provided any reliable information on bar width (vertical and horizontal) that is safe for horses. Grid bar width used in practice and recommended in the literature is based on empirical values and technical material properties. In this study, heads and hooves of 480 horses (233 mares, 204 geldings and 43 stallions) of 23 breeds were measured for making statements about the suitability of standard bar width, when considering the anatomy of the horse. It turned out that for vertical bars, an interspace of no more than five centimetres can be considered to be safe for all horses of a height of 110 centimetres and an age of two years and more. With horizontal lattice bars, a clear width of exactly 17 centimetres proved to be safe. This applies to all horses of a height of 148 centimetres and an age of two years or more. The clear widths of panels must be considered critical for horse welfare. When horses, for example, try to eat outside the panels and put their head through the bars, they may get stuck.] |
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Equine Behaviour @ team @ |
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6595 |
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Mench, J.A.; Morrow-Tesch, J.; Chu, L.-R. |
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Environmental enrichment for farm animals |
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Journal Article |
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1998 |
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Lab Animal |
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Lab Anim. |
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27 |
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32-36 |
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ISSN : 0093-7355 |
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Equine Behaviour @ team @ |
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6188 |
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