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Author |
Murphy, M.A.; Waits, L.P.; Kendall, K.C.; Wasser, S.K.; Higbee, J.A.; Bogden, R. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
An evaluation of long-term preservation methods for brown bear (Ursus arctos) faecal DNA samples |
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Journal Article |
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Year |
2002 |
Publication |
Conservation Genetics |
Abbreviated Journal |
Conservat. Genet. |
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3 |
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4 |
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435-440 |
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Relatively few large-scale faecal DNA studieshave been initiated due to difficulties inamplifying low quality and quantity DNAtemplate. To improve brown bear faecal DNA PCRamplification success rates and to determinepost collection sample longevity, fivepreservation methods were evaluated: 90%ethanol, DETs buffer, silica-dried, oven-driedstored at room temperature, and oven-driedstored at -20 °C. Preservationeffectiveness was evaluated for 50 faecalsamples by PCR amplification of a mitochondrialDNA (mtDNA) locus (~146 bp) and a nuclear DNA(nDNA) locus (~200 bp) at time points of oneweek, one month, three months and six months. Preservation method and storage timesignificantly impacted mtDNA and nDNAamplification success rates. For mtDNA, allpreservation methods had >= 75% success atone week, but storage time had a significantimpact on the effectiveness of the silicapreservation method. Ethanol preserved sampleshad the highest success rates for both mtDNA(86.5%) and nDNA (84%). Nuclear DNAamplification success rates ranged from 26-88%, and storage time had a significant impacton all methods but ethanol. Preservationmethod and storage time should be importantconsiderations for researchers planningprojects utilizing faecal DNA. We recommendpreservation of faecal samples in 90% ethanolwhen feasible, although when collecting inremote field conditions or for both DNA andhormone assays a dry collection method may beadvantageous. |
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1572-9737 |
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Equine Behaviour @ team @ Murphy2002 |
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6574 |
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Walpole, M.J.; Leader-Williams, N. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Tourism and flagship species in conservation |
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2002 |
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Biodivers Conserv |
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11 |
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Equine Behaviour @ team @ Walpole2002 |
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6446 |
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Sato, S.; Sako, S.; Maeda, A. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Social licking patterns in cattle (<em>Bos taurus</em>): influence of environmental and social factors |
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1991 |
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Applied Animal Behaviour Science |
Abbreviated Journal |
Applied Animal Behaviour Science |
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32 |
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1 |
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3-12 |
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To investigate the functions of social licking in cattle, four calves (one heifer and one steer in each of two herds), known to exhibit frequent social licking were observed continuously for 2 h before sunset for 13 days, using the focal animal sampling method. Calves were observed under various environmental conditions. Social licking significantly decreased on rainy days and tended to increase in a dirty barn and when food was restricted. Solicitation for social licking occurred not only from dominant animals of pairs but also from subordinates. Of the licking interactions, 31% occurred following solicitation, and these accounted for 39% of the total time spent licking. Following solicitation, 78% of social licking was oriented to the head and the neck regions that were inaccessible to self-licking animals. Unsolicited licking, however, was oriented not only to the head and the neck but also to the back and the rump regions, and these two latter regions were the major ones to receive licking. The effect of social relationships on social licking was investigated using least-squares analysis of variance. Social factors investigated were the difference of dominance values, the dominance-subordinance relationship, and kinship and familiarity; the sex of calves involved was also considered. Only familiarity had a significant effect on licking; exchanges of social licking increased with length of cohabitation. We suggest that social licking may have a cleaning effect, a tension-reducing effect and a bonding effect. |
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Elsevier |
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0168-1591 |
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doi: 10.1016/S0168-1591(05)80158-3 |
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Equine Behaviour @ team @ |
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6409 |
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Author |
Breitenmoser, U. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Large predators in the Alps: the fall and rise of man's competitors |
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1998 |
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Biol Conserv |
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83 |
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Equine Behaviour @ team @ Breitenmoser1998 |
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6450 |
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Harrington, F.H. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Aggressive howling in wolves |
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1987 |
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Anim Behav |
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35 |
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Equine Behaviour @ team @ Harrington1987 |
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6457 |
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Tooze, Z.J.; Harrington, F.H.; Fentress, J.C. |
![goto web page (via DOI) doi](img/doi.gif)
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Individually distinct vocalizations in timber wolves, Canis lupus |
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1990 |
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Anim Behav |
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40 |
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Equine Behaviour @ team @ Tooze1990 |
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6468 |
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Amodio, P.; Boeckle, M.; Schnell, A.K.; Ostojic, L.; Fiorito, G.; Clayton, N.S. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Grow Smart and Die Young: Why Did Cephalopods Evolve Intelligence? |
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Journal Article |
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2018 |
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Trends in Ecology & Evolution |
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Trends. Ecol. Evol. |
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Intelligence in large-brained vertebrates might have evolved through independent, yet similar processes based on comparable socioecological pressures and slow life histories. This convergent evolutionary route, however, cannot explain why cephalopods developed large brains and flexible behavioural repertoires: cephalopods have fast life histories and live in simple social environments. Here, we suggest that the loss of the external shell in cephalopods (i) caused a dramatic increase in predatory pressure, which in turn prevented the emergence of slow life histories, and (ii) allowed the exploitation of novel challenging niches, thus favouring the emergence of intelligence. By highlighting convergent and divergent aspects between cephalopods and large-brained vertebrates we illustrate how the evolution of intelligence might not be constrained to a single evolutionary route. |
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Elsevier |
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0169-5347 |
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doi: 10.1016/j.tree.2018.10.010 |
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Equine Behaviour @ team @ |
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6508 |
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Author |
Rosati, A.G. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Foraging Cognition: Reviving the Ecological Intelligence Hypothesis |
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Journal Article |
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2017 |
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Trends in Cognitive Sciences |
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Trends in Cognitive Sciences |
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21 |
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9 |
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691-702 |
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What are the origins of intelligent behavior? The demands associated with living in complex social groups have been the favored explanation for the evolution of primate cognition in general and human cognition in particular. However, recent comparative research indicates that ecological variation can also shape cognitive abilities. I synthesize the emerging evidence that ?foraging cognition? ? skills used to exploit food resources, including spatial memory, decision-making, and inhibitory control ? varies adaptively across primates. These findings provide a new framework for the evolution of human cognition, given our species? dependence on costly, high-value food resources. Understanding the origins of the human mind will require an integrative theory accounting for how humans are unique in both our sociality and our ecology. |
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1364-6613 |
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doi: 10.1016/j.tics.2017.05.011 |
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Equine Behaviour @ team @ |
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6586 |
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Dugnol, B.; Fernández, C.; Galiano, G.; Velasco, J. |
![goto web page (via DOI) doi](img/doi.gif)
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On a chirplet transform-based method applied to separating and counting wolf howls |
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2008 |
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Signal Process |
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88 |
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Equine Behaviour @ team @ Dugnol2008 |
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6466 |
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McGreevy, P.D.; Harman, A.; McLean, A.; Hawson, L. |
![goto web page (via DOI) doi](img/doi.gif)
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Title |
Over-flexing the horse's neck: A modern equestrian obsession? |
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Journal Article |
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2010 |
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Journal of Veterinary Behavior: Clinical Applications and Research |
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Journal of Veterinary Behavior: Clinical Applications and Research |
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5 |
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180-186 |
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We used an opportunistic review of photographs of different adult and juvenile horses walking, trotting, and cantering (n = 828) to compare the angle of the nasal plane relative to vertical in feral and domestic horses at liberty (n = 450) with ridden horses advertised in a popular Australian horse magazine (n = 378). We assumed that horses in advertisements were shown at, what was perceived by the vendors to be, their best. Of the ridden horses, 68% had their nasal plane behind the vertical. The mean angle of the unridden horses at walk, trot, and canter (30.7 ± 11.5; 27.3 ± 12.0; 25.5 ± 11.0) was significantly greater than those of the ridden horses (1.4 ± 14.1; ?5.1 ± ?11.1; 3.1 ± 15.4, P < 0.001). Surprisingly, unridden domestic horses showed greater angles than feral horses or domestic horses at liberty. We compared adult and juvenile horses in all 3 gaits and found no significant difference. Taken together, these findings demonstrate that the longitudinal neck flexion of the degree desirable by popular opinion in ridden horses is not a common feature of unridden horses moving naturally. Moreover, they suggest that advertised horses in our series are generally being ridden at odds with their natural carriage and contrary to the international rules of dressage (as published by the International Equestrian Federation). These findings are discussed against the backdrop of the established doctrine, which states that carrying a rider necessitates changes in longitudinal flexion, and in the context of the current debate around hyperflexion. |
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1558-7878 |
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doi: 10.1016/j.jveb.2010.03.004 |
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Equine Behaviour @ team @ |
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6501 |
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