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Streit, S., Zeitler-Feicht, M. H., & Dempfle, L. (2008). Gibt es in der Gruppenhaltung von Pferden bei der Abruffütterung am Automaten mehr Auseinandersetzungen als bei der Fütterung in Fressständen? [Keeping horses in groups, are there more confrontations when feeding is done with automatic feeding systems than with feeding stalls?]. In KTBL-Schriften (Vol. 471). KTBL.
Abstract: Das Droh- und Meideverhalten von 270 Pferden wurde im Fressbereich von 10 Offenlaufställen
mit Fressständen und 11 Offenlaufställen mit computergesteuerten Abrufstationen
anhand von visuellen kontinuierlichen Direktbeobachtungen erfasst. Diese erfolgten je Betrieb
über einen 24-Stunden-Tag, der nach dem Tortenstückverfahren (6x4 Stunden) zusammengesetzt
war.
Insgesamt wurden 6297 agonistische Verhaltensweisen in, vor und hinter den
Fütterungseinrichtungen registriert (Meiden 40,6 %, Verdrängen 12,8 %, Beißen/ Hinterhandschlag/
Angehen 12,7 % und Drohen/ Drohbeißen/ Hinterhanddrohen 33,9 %). In den
Futterstationen wurden 22,5 % dieses Verhaltens beobachtet, vor und hinter den Futterstationen
77,5 %. Bei den Betrieben mit Fressständen fanden 31 % der agonistischen Verhaltensweisen
in den Ständen statt, bei den Betrieben mit Abruffütterung 21 %.
Der Einfl uss des einzelnen Betriebes (innerhalb Fütterungssystem) auf die agonistischen
Verhaltensweisen vor und hinter den Fütterungseinrichtungen war signifi kant. Die Auswertung
ergab, dass Drohgesten im Wartebereich von Abrufstationen häufi ger auftreten
als in dem von Fressständen. Demgegenüber können Pferde in Abrufstationen ungestörter
fressen. Insgesamt betrachtet war jedoch die Anzahl an sozionegativen Interaktionen im
Bereich der Futtereinrichtungen bei beiden Fütterungssystemen gering. Die agonistischen
Verhaltensweisen wurden zusätzlich noch von der Heumenge und dem Konstitutionstyp
beeinfl usst.
Der Betrieb erwies sich als maßgeblicher Einfl ussfaktor. Als Resümee ergibt sich, dass
bei ordnungsgemäßer Gruppenhaltung mit fachgerechtem Management beide Fütterungssysteme
für Pferde im Offenlaufstall geeignet sind.
[The threatening and avoiding behaviour of 270 horses living in run-out sheds was observed
at 10 stables with feeding stalls and at 11 stables with automatic feeding systems for hay
and concentrates. Every group of horses was observed on five succeeding days visually
and immediately for 6 sessions, each of 4 hours. These 6 slices form together 24 hours, a
complete day.
Altogether, 6297 agonistic behaviour patterns were registered in front of, inside and
behind the feeding stations (avoiding behaviour 40.6 %, edging out of others 12.8 %,
Auseinandersetzungen an automatischer Abruffütterung und Fressständen
KTBL-Schrift 471 79
biting/rear leg kicking/charging 12.7 % und threatening/biting threats/rear leg kicking
threats 33.9 %). 22.5 % of these types of behaviour were recorded in the feeding stations,
77.5 % together in front and behind of these. In the stables with feeding stalls there were
31 % of the observed threatening gestures inside the feeding stations, in the stables with
automatic feeders only 21 %.
The individual farm showed signifi cant infl uence on the modes of agonistic behaviour
in front and behind the feeding facilities. Threatening gestures happen more often in the
waiting area of automatic feeders than in that of feeding stalls. On the other hand horses
in computer controlled systems will be less disturbed at eating. All together the number
of negative interactions in the feeding area at both feeding systems was relatively low.
In addition the agonistic behaviour was infl uenced by the quantity of hay and the constitutional
typ of the horses.
Because of the management of the individual stable exercises the most substantial
infl uence on the behaviour of the horses, it can be said, that, correct group keeping with
professional management provided, both feeding systems are suitable for horses in run-in
sheds.]
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Wehnert, C., Schmidt, A., Möstl, E., Aurich, J., Müller, J., & Aurich, C. (2008). Heart rate and cortisol release in horses during road transport. In IESM 2008.
Abstract: In sport horses, equestrian competitions may lead to increased cortisol release. The competition itself but also a new environment or transport to the events can be considered as stressors. In this study, warmblood sport horses (4-16 years, 4 mares, 2 stallions, 18 geldings) were transported by road for one (t1), 3.5 (t3.5) and 8 hours (t8), (n=8 per group). Heart rate (HR) is an indicator of stress and correlates with cortisol release. Heart rate was recorded with a mobile recording system (f810i, Polar, Kempele, Finland), fixed to a girth around the thorax of the horse and was monitored the day before transport, during transport and 12 hours thereafter. In addition, cortisol metabolite concentrations in faeces were determined in order to analyse adrenocortical activation during transport. Faecal samples were collected three times per day. Cortisol metabolite concentrations in faeces are increased approximately 24 hours after an elevation in plasma cortisol concentrations. Basal HR before transport did not differ between groups (45±2 (SEM) beats/min). During the first 30 min of transport, HR increased significantly (84±6, p<0.001, Kruskal-Wallis-H-test) but did not differ between groups. During the remaining part of the transport, HR was 61±6 beats/min (p<0.001 vs. first 30 min). When HR was analysed for the last 30 min of transport, values for groups t1 and t8 were significantly (p<0.05) higher than in group t3.5. HR decreased to baseline values within less than 30 min after transport and did not differ between groups (30-60 min after transport: 44±3 beats/min). Faecal cortisol metabolite concentrations on the day after transport were elevated compared to pre-transport baseline values in all three groups of horses. Significant differences existed between groups (e.g. 18 hours after transport t1: 91±5, t3.5: 110±18, t8: 136±27 ng/g; p<0.05). Based on HR analysis, horses of group t3.5 had adapted to transport, while the prolonged transport in group t8 again was a stressor. In group t1, which was transported only for one hour, the higher heart during the last 3 min of transport was still part of the initial rise in HR. After an initial increase, heart decreases indicating adaptation of the horse to transport. Cortisol metabolite concentrations in faeces indicate that transport causes adrenocortical activation with the amount of cortisol released depending on the duration of transport. Transport over medium distances appears to no major stressor and a negative impact on the performance of the horse is unlikely. Transport over 8 hours caused the most pronounced cortisol release and HR increases again during the last hours of an 8-hour transport. Transports exceeding this time may temporarily affect the subsequent performance of the horse in equestrian sports.
Supported by Stiftung Forschung für das Pferd
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Siniscalchi, M., Quaranta, A., & Rogers, L. J. (2008). Hemispheric specialization in dogs for processing different acoustic stimuli. PloS ONE, 3, e3349.
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Lloyd, A. S., Martin, J. E., Bornett-Gauci, H. L. I., & Wilkinson, R. G. (2008). Horse personality: Variation between breeds. Appl. Anim. Behav. Sci., 112(3-4), 369–383.
Abstract: Anecdotal evidence from horse owners and handlers suggests the existence of breed typical behaviour and personality in horses. This is further supported by current research on heritability of personality characteristics in a range of species. The Horse Personality Questionnaire (HPQ) is a 25-item rating method that has previously been shown to be reliable for the assessment of personality in horses. Principal component analysis on HPQ data has identified six underlying personality components in horses. These are Dominance, Anxiousness, Excitability, Protection, Sociability and Inquisitiveness. Using the HPQ a survey of 1223 horses of eight different breeds was completed. Data were analysed to explore any differences in personality between breeds across the six personality components. Breed differences in personality were identified, and it was noted that variability between breeds varied between personality components. Anxiousness and Excitability showed the most variation between breeds, whilst Dominance and Protection showed the least variance. The results identified breed typical personalities that were comparable to results from previous studies as well as anecdotal evidence provided by the popular equine literature. The results are discussed in terms of the potential selection pressures that may have resulted in these differences.
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Krueger, K., & Heinze, J. (2008). Horse sense: social status of horses (Equus caballus) affects their likelihood of copying other horses` behavior. Anim. Cogn., 11(3), 431–439.
Abstract: Animals that live in stable social groups need to gather information on their own relative position in the group`s social hierarchy, either by directly threatening or challenging others, or in a less costly manner, by observing interactions among others. Such indirect inference of dominance relationships has previously been reported from primates, rats, and birds and fish. Here, we show that domestic horses, Equus caballus, are similarly capable of social cognition. Taking advantage of a specific “following behavior” that horses show towards humans in a riding arena, we investigated whether bystander horses adjust their response to an experimenter according to the observed interaction and their own dominance relationship with the horse whose reaction to the experimenter they had observed before. Horses copied the following behavior towards an experimenter after watching a dominant horse following, but did not follow after observing a subordinate horse or a horse from another social group doing so. The following behavior which horses show towards an experimenter therefore appears to be affected by the demonstrator`s behavior and social status relative to the observer.
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Proops, L., McComb, K., & Reby, D. (2008). Horse-human interactions: Attention attribution and the use of human cues by domestic horses (Equus caballus). In IESM 2008.
Abstract: Recent research has shown that domestic dogs are particularly good at reading human attentional cues, often outperforming chimpanzees and hand reared wolves [1, 2]. It has been suggested that the close evolutionary relationship between humans and dogs has led to the development of this ability, however very few other species have been studied [3]. We tested the ability of 24 domestic horses to discriminate between an attentive and inattentive person when choosing whom to approach for food. While the attentive person faced forwards, the inattentive person either stood with their body turned 180° away from the subject (body orientation condition), stood with their body facing forwards but their head facing away (head orientation condition) or stood facing forwards but with their eyes closed (eyes closed condition). A fourth, mixed condition was included where the attentive person stood with their body facing away from the subjects but their head turned towards the subject while the inattentive person stood with their body facing the subject but their head turned away. Horses chose the attentive person significantly more often using the body cue (n = 24, k = 19, p = 0.003), the head cue (n = 24, k = 18, p = 0.011), and the eye cue (n = 24, k = 19, p = 0.003) but not the mixed cue (n = 24, k = 13, p = 0.42). In an additional pilot study, horses were tested in an object choice task. A human experimenter cued one of two buckets by either tapping the bucket (tap condition), orienting their body towards the bucket and pointing (body and point condition), pointing while facing forwards (point condition) or orienting their body towards the bucket (body condition). If the subjects chose the correct bucket they were rewarded. Subjects were able to use the tap cue (n = 31, k = 21, p = 0.035), body + point cue (n= 31, k = 21, p = 0.035) and the point cue (n = 30, k = 21, p = 0.021) but not the body cue (n = 31, k = 11, p = 0.076). These results taken together suggest that domestic horses are also very sensitive to human attentional cues, including gaze.
Keywords:
social cognition, animal-human interaction, horses, attention attribution, domestication
1. Hare, B., Brown, M., Williamson, C., and Tomasello, M. (2002). The domestication of social cognition in dogs. Science 298, 1634-1636.
2. Gacsi, M., Miklosi, A., Varga, O., Topal, J., and Csanyi, V. (2004). Are readers of our face readers of our minds` Dogs (Canis familiaris) show situation-dependent recognition of human’s attention. Animal Cognition 7, 144-153.
3. Hare, B., and Tomasello, M. (2005). Human-like social skills in dogs? Trends Cogn. Sci. 9, 439-444.
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Hazard, H. (2008). Horses: Companions for Life. In IESM 2008.
Abstract: The Humane Society United States (HSUS) has been partnering with several prominent researchers for over 20 years to assess the potential use of Porcine Zona Pellucida (PZP), a protein used as a fertility control vaccine for wild horses. Past studies on herds located on barrier islands of the eastern United States have demonstrated that PZP prevented pregnancies and was a valuable tool for population management. With the generous support of the Annenberg Foundation and in partnership with the Science and Conservation Center, Tufts University and The University of Toledo, HSUS is conducting a 5-year longitudinal study to assess the effectiveness of immunocontraception on over 600 wild horses in the western United States.
This project involves 2 herds of over 300 wild horses each located in Utah and Colorado. We began gathering pre treatment data in April 2008. Birth rates, band size, and individual horse identifications were recorded. In the winter of 2008/2009 both herds will be captured and all mares that are released will be treated with a 2-year-duration PZP vaccine. Both herds will be closely monitored for reproduction and behavior changes for 3 years. We will record the differences in reproductive success of treated and untreated (not captured) females.
HSUS is also seeking to develop refinements to the PZP vaccine and delivery technologies. HSUS is currently trying to improve the production of the PZP vaccine by producing it with techniques that are more efficient and less costly. Improving delivery methods for the 2 year drug is another goal of this research that may allow herd managers the flexibility of treating mares year round without having to capture it. HSUS also hopes to demonstrate that incorporating this new delivery method and proactively managing wild horse herds will assist in maintaining wild horse populations at a level that is sustainable and manageable.
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Gaunet, F. (2008). How do guide dogs of blind owners and pet dogs of sighted owners ( Canis familiaris ) ask their owners for food? Anim. Cogn., 11(3), 475–483.
Abstract: Abstract Although there are some indications that dogs (Canis familiaris) use the eyes of humans as a cue during human–dog interactions, the exact conditions under which this holds true are unclear. Analysing whether the interactive modalities of guide dogs and pet dogs differ when they interact with their blind, and sighted owners, respectively, is one way to tackle this problem; more specifically, it allows examining the effect of the visual status of the owner. The interactive behaviours of dogs were recorded when the dogs were prevented from accessing food that they had previously learned to access. A novel audible behaviour was observed: dogs licked their mouths sonorously. Data analyses showed that the guide dogs performed this behaviour longer and more frequently than the pet dogs; seven of the nine guide dogs and two of the nine pet dogs displayed this behaviour. However, gazing at the container where the food was and gazing at the owner (with or without sonorous mouth licking), gaze alternation between the container and the owner, vocalisation and contact with the owner did not differ between groups. Together, the results suggest that there is no overall distinction between guide and pet dogs in exploratory, learning and motivational behaviours and in their understanding of their owner’s attentional state, i.e. guide dogs do not understand that their owner cannot see (them). However, results show that guide dogs are subject to incidental learning and suggest that they supplemented their way to trigger their owners’ attention with a new distal cue.
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Pongrácz, P., Vida, V., Bánhegyi, P., & Miklósi, Á. (2008). How does dominance rank status affect individual and social learning performance in the dog (Canis familiaris)? Anim. Cogn., 11, 75–82.
Abstract: Dogs can learn effectively to detour around a V-shaped fence after observing a demonstration from either an unfamiliar human or dog demonstrator. We found earlier that there is substantial individual variation between the dogs' performance, even when using the same experimental conditions. Here, we investigate if the subjects' relative dominance rank with other dogs had an effect on their social learning performance. On the basis of the owners' answers to a questionnaire, subjects from multi-dog homes were sorted into groups of dominant and subordinate dogs. In Experiment 1, dominant and subordinate dogs were tested without demonstration and we did not find any difference between the groups-they had similarly low detour performances on their own. In Experiment 2 and 3, dogs from single dog and multi-dog households were tested in the detour task with demonstration by an unfamiliar dog, or human, respectively. The results showed that social learning performance of the single dogs fell between the dominant and subordinate multi-dogs with both dog and human demonstration. Subordinate dogs displayed significantly better performance after having observed a dog demonstrator in comparison to dominant dogs. In contrast, the performance of dominant and subordinate dogs was almost similar, when they observed a human demonstrator. These results suggest that perceived dominance rank in its own group has a strong effect on social learning in dogs, but this effect seems to depend also on the demonstrator species. This finding reveals an intricate organization of the social structure in multi-dog households, which can contribute to individual differences existing among dogs.
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Milinski, M., & Rockenbach, B. (2008). Human behaviour: Punisher pays. Nature, 452(7185), 297–298.
Abstract: The tendency of humans to punish perceived free-loaders, even at a cost to themselves, is an evolutionary puzzle: punishers perish, and those who benefit the most are those who have never punished at all.
Humans are champions of cooperation. Reciprocity – the idea that, if I help you this time, you'll help me next time1 – is a secret of our success.
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