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Author |
Taberlet, P.; Waits, L.P.; Luikart, G. |
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Title |
Noninvasive genetic sampling: look before you leap |
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Journal Article |
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Year |
1999 |
Publication |
Trends in Ecology & Evolution |
Abbreviated Journal |
Trends Ecol. Evol |
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14 |
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8 |
Pages |
323-327 |
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Keywords |
Hairs; Feces; Feathers; Allelic dropout; Individual identification; Conservation genetics; Behavioural ecology; Pilot study; Microsatellites; Probability of identity |
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Noninvasive sampling allows genetic studies of free-ranging animals without the need to capture or even observe them, and thus allows questions to be addressed that cannot be answered using conventional methods. Initially, this sampling strategy promised to exploit fully the existing DNA-based technology for studies in ethology, conservation biology and population genetics. However, recent work now indicates the need for a more cautious approach, which includes quantifying the genotyping error rate. Despite this, many of the difficulties of noninvasive sampling will probably be overcome with improved methodology. |
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0169-5347 |
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Equine Behaviour @ team @ |
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6573 |
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Author |
Krueger, K.; Esch, L.; Byrne, R. |
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Title |
Animal behaviour in a human world: A crowdsourcing study on horses that open door and gate mechanisms |
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Journal Article |
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Year |
2019 |
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Plos One |
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Plos One |
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14 |
Issue |
6 |
Pages |
e0218954 |
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Anecdotal reports of horses opening fastened doors and gates are an intriguing way of exploring the possible scope of horses' problem-solving capacities. The species' natural environment has no analogues of the mechanisms involved. Scientific studies on the topic are missing, because the rate of occurrence is too low for exploration under controlled conditions. Therefore, we compiled from lay persons case reports of horses opening closed doors and gates. Additionally, we collected video documentations at the internet platform YouTube, taking care to select raw data footage of unedited, clearly described and clearly visible cases of animals with no distinct signs of training or reduced welfare. The data included individuals opening 513 doors or gates on hinges, 49 sliding doors, and 33 barred doors and gateways; mechanisms included 260 cases of horizontal and 155 vertical bars, 43 twist locks, 42 door handles, 34 electric fence handles, 40 carabiners, and 2 locks with keys. Opening was usually for escape, but also for access to food or stable-mates, or out of curiosity or playfulness. While 56 percent of the horses opened a single mechanism at one location, 44 percent opened several types of mechanism (median = 2, min. = 1, max. = 5) at different locations (median = 2, min. = 1, max. = 4). The more complex the mechanism was, the more movements were applied, varying from median 2 for door handles to 10 for carabiners. Mechanisms requiring head- or lip-twisting needed more movements, with significant variation between individuals. 74 horses reported in the questionnaire had options for observing the behaviour in stable mates, 183 did not, which indicates that the latter learned to open doors and gates either individually or from observing humans. Experience favours opening efficiency; subjects which opened several door types applied fewer movements per lock than horses which opened only one door type. We failed to identify a level of complexity of door-fastening mechanism that was beyond the learning capacity of the horse to open. Thus, all devices in frequent use, even carabiners and electric fence handles, are potentially vulnerable to opening by horses, something which needs to be considered in relation to keeping horses safely. |
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Public Library of Science |
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Equine Behaviour @ team @ |
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6580 |
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Leliveld, L.M.C.; Düpjan, S.; Tuchscherer, A.; Puppe, B. |
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Title |
Hemispheric Specialization for Processing the Communicative and Emotional Content of Vocal Communication in a Social Mammal, the Domestic Pig |
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Journal Article |
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2020 |
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Frontiers in Behavioral Neuroscience |
Abbreviated Journal |
Front. Behav. Neurosci. |
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14 |
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596758 |
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In humans, speech perception is lateralized, with the left hemisphere of the brain dominant in processing the communicative content and the right hemisphere dominant in processing the emotional content. However, still little is known about such a division of tasks in other species. We therefore investigated lateralized processing of communicative and emotionally relevant calls in a social mammal, the pig (Sus scrofa). Based on the contralateral connection between ears and hemispheres, we compared the behavioural and cardiac responses of 36 young male pigs during binaural and monaural (left or right) playback to the same sounds. The playback stimuli were calls of social isolation and physical restraint, whose communicative and emotional relevance, respectively, were validated prior to the test by acoustic analyses and during binaural playbacks. There were indications of lateralized processing mainly in the initial detection (left head-turn bias, indicating right hemispheric dominance) of the more emotionally relevant restraint calls. Conversely, there were indications of lateralized processing only in the appraisal (increased attention during playback to the right ear) of the more communicative relevant isolation calls. This implies differential involvement of the hemispheres in the auditory processing of vocalizations in pigs and thereby hints at similarities in the auditory processing of vocal communication in non-human animals and speech in humans. Therefore, these findings provide interesting new insight in the evolution of human language and auditory lateralization. |
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1662-5153 |
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Equine Behaviour @ team @ |
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6699 |
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Author |
Nakagawa, S. |
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A farewell to Bonferroni: the problems of low statistical power and publication bias |
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2004 |
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Behav Ecol |
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15 |
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Equine Behaviour @ team @ Nakagawa2004 |
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6294 |
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Range, F.; Möslinger, H.; Virányi, Z. |
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Domestication has not affected the understanding of means-end connections in dogs |
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2012 |
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Anim Cogn |
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15 |
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Equine Behaviour @ team @ Range2012 |
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6322 |
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Author |
Nakagawa, S. |
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Title |
A farewell to Bonferroni: the problems of low statistical power and publication bias |
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2004 |
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Behavioral Ecology |
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beheco |
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15 |
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6 |
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1044-1045 |
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1045-2249 |
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Equine Behaviour @ team @ |
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6560 |
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Author |
Byrne, R.W. |
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Title |
Do larger brains mean greater intelligence? |
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Journal Article |
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Year |
1993 |
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Behavioral and Brain Sciences |
Abbreviated Journal |
Behav. Brain Sci. |
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16 |
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4 |
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696-697 |
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Cambridge University Press |
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1469-1825 |
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Equine Behaviour @ team @ |
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6171 |
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Blakeman, N.E.; Friend, T.H. |
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Visual discrimination at varying distances in Spanish goats |
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1986 |
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Appl Anim Behav Sci |
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16 |
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Equine Behaviour @ team @ Blakeman1986 |
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6251 |
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Van Schaik, C.P.; Isler, K.; Burkart, J.M. |
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Title |
Explaining brain size variation: from social to cultural brain |
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2012 |
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Trends Ecol Evol |
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16 |
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Equine Behaviour @ team @ Van Schaik2012 |
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6304 |
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Janczarek, I.; Stachurska, A.; Kedzierski, W.; Wisniewska, A.; Ryzak, M.; Koziol, A. |
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Title |
The intensity of physiological and behavioral responses of horses to predator vocalizations |
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2020 |
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BMC Veterinary Research |
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16 |
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1 |
Pages |
431 |
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Predatory attacks on horses can become a problem in some parts of the world, particularly when considering the recovering gray wolf populations. The issue studied was whether horses transformed by humans and placed in stable-pasture environments had retained their natural abilities to respond to predation risk. The objective of the study was to determine the changes in cardiac activity, cortisol concentrations, and behavior of horses in response to the vocalizations of two predators: the gray wolf (Canis lupus), which the horses of the breed studied had coevolved with but not been exposed to recently, and Arabian leopard (Panthera pardus nimr), from which the horses had been mostly isolated. In addition, we hypothesized that a higher proportion of Thoroughbred (TB) horse ancestry in the pedigree would result in higher emotional excitability in response to predator vocalizations. Nineteen horses were divided into groups of 75%, 50% and 25% TB ancestry. The auditory test conducted in a paddock comprised a 10-min prestimulus period, a 5-min stimulus period when one of the predators was heard, and a 10-min poststimulus period without any experimental stimuli. |
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1746-6148 |
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Equine Behaviour @ team @ Janczarek2020 |
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6624 |
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