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Merola, I.; Lazzaroni, M.; Marshall-Pescini, S.; Prato-Previde, E. |
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Social referencing and cat–human communication |
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Journal Article |
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2015 |
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Animal Cognition |
Abbreviated Journal |
Anim. Cogn. |
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18 |
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3 |
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639-648 |
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Social referencing; Cats; Gaze alternation; Social learning; Human–cat communication |
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Cats’ (Felis catus) communicative behaviour towards humans was explored using a social referencing paradigm in the presence of a potentially frightening object. One group of cats observed their owner delivering a positive emotional message, whereas another group received a negative emotional message. The aim was to evaluate whether cats use the emotional information provided by their owners about a novel/unfamiliar object to guide their own behaviour towards it. We assessed the presence of social referencing, in terms of referential looking towards the owner (defined as looking to the owner immediately before or after looking at the object), the behavioural regulation based on the owner’s emotional (positive vs negative) message (vocal and facial), and the observational conditioning following the owner’s actions towards the object. Most cats (79 %) exhibited referential looking between the owner and the object, and also to some extent changed their behaviour in line with the emotional message given by the owner. Results are discussed in relation to social referencing in other species (dogs in particular) and cats’ social organization and domestication history. |
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Springer Berlin Heidelberg |
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English |
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1435-9448 |
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Equine Behaviour @ team @ |
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5885 |
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Meek, P.D.; Ballard, G.-A.; Fleming, P.J.S. |
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Title |
The pitfalls of wildlife camera trapping as a survey tool in Australia |
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Journal Article |
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2015 |
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Australian Mammalogy |
Abbreviated Journal |
Aust. Mammal. |
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37 |
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1 |
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13-22 |
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camera trap constraints, critical review, remote cameras. |
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Camera trapping is a relatively new addition to the wildlife survey repertoire in Australia. Its rapid adoption has been unparalleled in ecological science, but objective evaluation of camera traps and their application has not kept pace. With the aim of motivating practitioners to think more about selection and deployment of camera trap models in relation to research goals, we reviewed Australian camera trapping studies to determine how camera traps have been used and how their technological constraints may have affected reported results and conclusions. In the 54 camera trapping articles published between 1991 and 2013, mammals (86%) were studied more than birds (10%) and reptiles (3%), with small to medium-sized mammals being most studied. Australian camera trapping studies, like those elsewhere, have changed from more qualitative to more complex quantitative investigations. However, we found that camera trap constraints and limitations were rarely acknowledged, and we identified eight key issues requiring consideration and further research. These are: camera model, camera detection system, camera placement and orientation, triggering and recovery, camera trap settings, temperature differentials, species identification and behavioural responses of the animals to the cameras. In particular, alterations to animal behaviour by camera traps potentially have enormous influence on data quality, reliability and interpretation. The key issues were not considered in most Australian camera trap papers and require further study to better understand the factors that influence the analysis and interpretation of camera trap data and improve experimental design. |
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Equine Behaviour @ team @ |
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6704 |
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Medill, S.A; Janz, D.M.; McLoughlin, P.D. |
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Hair testosterone and cortisol concentrations and their relationships to physiological and social status in feral horses (Equus ferus caballus) |
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Conference Article |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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Determining steroid hormone concentrations in hair has been frequently performed in humans, and increasingly in wildlife and domestic animals. Hair hormone concentrations may provide insight on how individuals are responding to their physiological condition or social situation. Cortisol is most frequently measured in hair as a biomarker of long-term stress, while testosterone may be linked with reproductive status in males. These hormones are commonly measured in substances that reflect either current (e.g. blood) or very recent (e.g. saliva, urine, feces) circulating levels. However, these hormones are also incorporated into hair during hair growth and provide a chronological record of circulating hormone levels. Thus, analysis of steroid hormones in hair provides a much longer representation of an animal’s endocrine status than other tissues frequently targeted for non-invasive monitoring.
The feral horse (Equus ferus caballus) population on Sable Island, Nova Scotia, Canada, has been annually censused during the mid-late summer since 2008 to track individual life histories and population dynamics. We collected tail hair (n = 144 females, n = 162 males) from known individuals either opportunistically or from natural or artificial snags to investigate how hair cortisol and testosterone might be associated with physiological state (e.g. lactating vs. non-lactating, body condition, age), as well as their social situation (e.g. dominant band stallion, subordinate band stallion, or bachelor) and measures of sociality. The proximal 5 cm of hair (excluding first 4mm or root region) were ground to a fine powder and hormones extracted with methanol and analyzed by using enzyme-linked immunoassay.
Preliminary analyses of the data showed a general sex based difference in hair cortisol concentrations (females lower than males; t = 3.16, df = 317, P=0.002). Among females, the presence of nursing foals was accompanied by an increase in hair cortisol (z = 2.93, df =140, P = 0.003); however, no significant difference was found in hair cortisol concentrations based on sex of the foal (t = -0.06, df = 82, P = 0.95). Horses in poor body condition tended to have higher hair cortisol than those in good or excellent condition (slope= -0.203, df = 312, P = 0.003). We also observed an increased concentration of hair cortisol as horses increased in age from 3-6 or entered into reproductive maturity. Adult male dominant band stallions did not have significantly less cortisol than bachelors or subordinate stallions but these three groups were significantly greater than young males (aged 3 and 4) who generally do not challenge the older males for reproductive opportunities.
Additionally, we looked at hair testosterone concentrations for n=46 males. Testosterone is known to influence traits and behaviours that enhance sexual selection. Often there is an inverse relationship between cortisol levels and testosterone; in particular, being able to maintain high testosterone and not have elevated cortisol related to the metabolic costs of sexual trait production ensures that traits or behaviours honestly signal the quality of the individual. For this reason we’d expect to see band stallions (those males in a position to mate) have a lower value in the ratio Cortisol: Testosterone. Early indications suggest we see this phenomenon in feral horses.
As a relatively new approach in wildlife research, the use of hair hormone analysis shows promise in contributing to our understanding of physiological aspects of sexual selection and other processes. Additionally, hair hormone analysis may have applications in advancing knowledge of animal husbandry and in particular, welfare. |
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Medill, S.A. |
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Equine Behaviour @ team @ |
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5870 |
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McComb, K. |
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Social cognition and emotional awareness: studies on elephants and horses |
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Conference Article |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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McComb, K. |
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Xenophon Publishing |
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Wald |
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Krueger, K. |
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Proc. 3. Int. Equine. Sci. Mtg |
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in prep |
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978-3-95625-000-2 |
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Equine Behaviour @ team @ |
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5800 |
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Maros, K.; Kovács, R.; Nagy, K. |
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Questionnaire survey personality assessment of horses of different use |
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Conference Article |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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horse, personality, questionnaire, |
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We collected data from 248 horses of different breeds, age, sex and use, forming four groups: 74 trotters, 70 gallop horses, 60 horseback archery horses and 44 police horses. All horses were trained and ridden/driven in a regular base. Caretakers or owners who were familiar with the target animals were asked to assess their horses’ temperament. The temperament scores were obtained with the 7-point scale questionnaire according to the Horse Personality Questionnaire which has 25 items and has previously been shown to be reliable for the assessment of personality in horses. It measures six personality components in horses: Dominance, Anxiousness, Excitability, Protection, Sociability and Inquisitiveness.
Component scores were calculated according to Lloyd, A.S., Martin, J.E., Bornett-Gauci, H.L.I., Wilkinson, R.G. (2008) Horse personality: Variation between breeds. Applied Animal Behaviour Science 112. 369–383. The component scores were compared across the four examined groups using the Kruskal–Wallis test. Post hoc multiple comparisons tests were then carried out to explore specific breed differences on each component. The value of alpha was set at 0.05 for all statistical tests.
Groups differed significantly regarding Anxiousness and Excitability, but no significant differences were found regarding Dominance, Protection, Sociability or Inquisitiveness among groups. This finding is in line with the findings of Lloyd et al. (2008) who showed that Anxiousness and Excitability components have the highest level of variation between breeds.In our study, gallop horses had the highest rank regarding Excitability and they differed significantly from police horses which had the lowest rank for this personality component. Interestingly gallop horses had the lowest rank regarding Anxiousness, and trotters got the highest rank in in this component.
According to our results gallop horses are the most extreme in their personality. It is conceivable that being excitable is a more favourable trait for a race horse than for a working police horse. However, it is interesting that trotters are more anxious than gallop horses since they also have a high thoroughbred ancestry. The effect of work and training on these horses needs further surveys. |
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Maros, K. |
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Xenophon Publishing |
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Wald |
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Krueger, K. |
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978-3-95625-000-2 |
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Equine Behaviour @ team @ |
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5904 |
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Malavasi, R.; Huber, L. |
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Referential communication in the domestic horse (Equus caballus): first exploration in an ungulate species |
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Conference Article |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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domestic horse, referential communication, human-horse communication, intentionality |
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An important question in the study of animal communication is whether non-human animals are able to produce communicative gestures, i.e. nonvocal bodily actions directed to a recipient, physically ineffective but with a meaning shared in the social group [1]. Passive gestures are instrumental, tuned to the mere presence/absence of others, whereas active informers recognize receivers as communicative agents and activate shared-attention mechanisms for identifying their attentional state (SAM [2]; e.g. Schwab and Huber [3]). Six operational criteria must be evaluated to classify a signal as referential and intentional [4]: (1) alternative gazes between the partner and the target; (2) apparent attention-getting behaviours are deployed; (3) an audience is required to exhibit the behaviour; (4) the attentional status of an observer influences the propensity to exhibit behaviours; (5) communication is persistent and (6) there is elaboration of communicative behaviour when apparent attempts to manipulate the partner fail. Dogs [5] and non-human primates (reviewed in Liebal and Call [6]) can tune a human receiver’s attention to the object of interest by combining directional and attention-getting signals, such as turning the head or body, gazing to the receiver, and/or establishing eye contact. Research on other species is scarce.
Horses rely on humans to survive in domestic settings and may have evolved skills for communicating flexibly with them [7]. Horses understand human attentional cues (such as body and head orientation, eyes opened/closed) [8], permanent pointing [9] and, to some extent, gazing [10]. Here we tested the ability of 14 outdoor, herd-living domestic horses to communicate referentially with a human partner about the location of a desired target, a bucket of food out of reach. After the baiting of two buckets placed in opposite, unreachable locations were shown by the experimenter, the subject would walk to one of the two buckets. Because approaching a bucket would reveal that the food is out of reach, we expected the horse to look back to the experimenter, then to the bucket, and alternate this gazing several times to indicate its intention. To test whether our prediction is correct and alternate gazing is indeed the result of the horse's referential communication, we video-recorded the behaviour of the subjects in the test (FORWARD) and three control conditions: (1) FORWARD: experimenter oriented to the center of the arena, (2) BACK: experimenter backward oriented in respect to the arena, (3) ALONE: experimenter absent, (4) MANY: as FORWARD plus a familiar human oriented to the subject behind the bucket (Figure 1). We used a conservative criterion of back gazing by considering only turning the head back more than 90 degrees. The results confirmed our prediction. The horses alternated gazes between the partner and the buck significantly more often in the FORWARD than in all the other conditions (Table 1), thus satisfying operational criteria #1, #3 and #4. They also alternated head nods with gazes to the partner significantly more often during the FORWARD condition. We thus considered head nods not an instrumental signal of arousal, but an attention-getting behaviour with communicative function. Subjects used both head nods and neck stretched toward the buck more often in the FORWARD than in the BACK and the ALONE conditions, thus satisfying criteria #2, #3 and #4. In condition MANY, the frequency of head nods did not differ from condition FORWARD, probably because nods were directed to the additional partner behind the buck. This also satisfies criteria #4. The horses gazed to the partner most often in the FORWARD than in the BACK and the MANY conditions, but not in the ALONE. In this condition, subjects could observe the partner walking further from the test arena. To test for the different functions of gazes in presence and in absence of the partner, we compared their average duration between the two conditions: the significantly longer duration of gazes when the subject was alone suggests the instrumental monitoring function of gazes in this experimental condition.
Altogether, the findings suggest that domestic horses possess the ability to use referential communication in an interspecific context, but additional analyses are needed to test for operational criteria #5 and #6. Flexible and voluntary use of communicative signals reveal sophisticated cognitive processes involved in the strategic emission of these signals, and the finding of referential communication skills in an ungulate species forces us to reconsider the evolutionary path of intelligence. Furthermore, ungulates are used intensively by humans (transportation, meat, agriculture, leisure activities), and their welfare is often compromised. Determining whether ungulates can communicate their needs and preferences is paramount to a proper ethical management. |
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Malavasi, R. |
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Equine Behaviour @ team @ |
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5876 |
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Lovrovich, P.; Sighieri, C.; Baragli, P. |
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Following human-given cues or not? Horses (Equus caballus) get smarter and change strategy in a delayed three choice task |
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2015 |
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Applied Animal Behaviour Science |
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Appl. Anim. Behav. Sci. |
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166 |
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80-88 |
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Highlights
�Horses remember the location of food hidden by the experimenter after a delay.
�They understand the communicative meaning of a human positioned close to the target.
�The same horses are capable of changing their decision-making strategy.
�They are able to shift from accuracy inferred from human given cues to speed.
�Horses can use human cues or not depending on time, cost, experience and reward.
Abstract
To date, horses have seemed capable of using human local enhancement cues only when the experimenter remains close to the reward, since they fail to understand the communicative meaning of the human as momentary local enhancement cue (when the human is not present at the moment of the animal's choice). This study was designed to analyse the ability of horses to understand, remember and use human-given cues in a delayed (10 s) three-choice task. Twelve horses (experimental group) had to find a piece of carrot hidden under one of three overturned buckets after seeing the experimenter hide it. The results were then compared with those of a control group (twelve horses) that had to find the carrot using only the sense of smell or random attempts. At the beginning, the experimental horses made more correct choices at the first attempt, although they took more time to find the carrot. Later the same horses were less accurate but found the carrot in less time. This suggests that the value of the proximal momentary local enhancement cues became less critical. It seemed, in fact, that the experimental and control group had aligned their behaviour as the trials proceeded. Despite this similarity, in the second half of the trials, the experimental group tended to first approach the bucket where they had found the carrot in the immediately preceding trial. Our findings indicate that horses are capable of remembering the location of food hidden by the experimenter after a delay, by using the human positioned close to the target as valuable information. The same horses are also capable of changing their decision-making strategy by shifting from the accuracy inferred from human given cues to speed. Therefore, horses are able to decide whether or not to use human given-cues, depending on a speed-accuracy trade-off. |
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Elsevier |
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doi: 10.1016/j.applanim.2015.02.017 |
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Equine Behaviour @ team @ |
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5849 |
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Lee, P.C.; de Antonio, C. A. |
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Necessity, unpredictability and opportunity: An exploration of ecological and social drivers of behavioral innovation. |
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2015 |
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Animal Creativity and Innovation |
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317- 333 |
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Cambridge |
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Equine Behaviour @ team @ |
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6535 |
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Leadbeater, E. |
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What evolves in the evolution of social learning? |
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2015 |
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Journal of Zoology |
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J Zool |
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295 |
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4-11 |
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social learning; associative learning; social information use |
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Social learning is fundamental to social life across the animal kingdom, but we still know little about how natural selection has shaped social learning abilities on a proximate level. Sometimes, complex social learning phenomena can be entirely explained by Pavlovian processes that have little to do with the evolution of sociality. This implies that the ability to learn socially could be an exaptation, not an adaptation, to social life but not that social learning abilities have been left untouched by natural selection. I discuss new empirical evidence for associative learning in social information use, explain how natural selection might facilitate the associative learning process and discuss why such studies are changing the way that we think about social learning. |
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Equine Behaviour @ team @ |
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6015 |
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König von Borstel, U.; Küllmar, A. |
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A pilot study on horses‘ behaviour and distance travelled in a “Paddock Trail” husbandry system |
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2015 |
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Proceedings of the 3. International Equine Science Meeting |
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Proc. 3. Int. Equine. Sci. Mtg |
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With most modern horse husbandry systems, horses’ locomotory behavior is quantitatively as well as qualitatively considerably altered, compared to the slow and continuous movement shown by horses living under conditions similar to those they have evolved under. This lack of locomotion as well as the change in quality of locomotion is thought to be responsible for a number of health issues seen in present day horses. The aim of the present study was to assess behaviour and particularly locomotion in horses kept in a husbandry system specifically designed to stimulate locomotory behaviour in horses. This type of husbandry system is named “Paddock Trail”, (PT) but is also known as “Paddock Paradise”, and the key concept of this husbandry system involves strategic placement of small portions of feed along a track which is an integral part of this husbandry system. For the present study, 11 horses, not used for riding or other activities and kept in one Paddock Trail husbandry system were available. Seven horses used in equine assisted therapy lessons and housed individually in conventional paddock-boxes (IB) served as a control group. Both groups of horses were composed of a similar mixture of horses with regard to age and breeds. Using time-sampling, behaviour of the horses was observed in 8 bouts (4 morning and 4 afternoon sessions) of 5 hours each. In addition, the average speed and distance covered was assessed in 3 (PT) and 5 (IB) horses, respectively, using a GPS system. Since the GPS signal is blocked by buildings and reliable recording would not be possible indoors, the IB horses were recorded only during their work in the therapy sessions. The behavioural observations revealed that the PT horses allocated a larger proportion of time to locomotory behaviour compared to the IB horses (on average 12 vs 3% of the 5 h observation periods; P<0,05), and in turn resting behaviour was reduced in PT horses compared to IB horses (30 vs. 46%; P<0,05). Time spent grazing (10 vs. 8%) and feeding other than grazing (47 vs. 44%) did not differ significantly between the two groups of horses in the two different husbandry systems (P>0,1). In addition, resting and feeding behaviour was influenced by social rank, such that higher ranking horses spent more time feeding and less time resting compared to horses of lower ranks (both P<0,05). Within the 5 hour observation periods, horses of the PT system covered on average a distance of 2,7 km at an average speed of 0,5 km/h. In comparison, IB horses covered during their work in the therapy sessions on average a distance of 2,1 km at an average speed of 3,6 km/h for a duration of 35 minutes. Although the confounding of groups of horses with husbandry system and although the GPS data does not allow for a direct comparison of the husbandry systems and does not cover the entire 24 hours of a day, these data indicate along with the behavioural observations that the PT system stimulates the horses to increase their locomotory behaviour.
Keywords horse, husbandry, paddock trail, locomotion, behaviour |
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König von Borstel, U. |
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Xenophon Publishing |
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Wald |
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; Krueger, K. |
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978-3-95625-000-2 |
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Equine Behaviour @ team @ |
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5898 |
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