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Napolitano, F., De Rosa, G., Braghieri, A., Grasso, F., Bordi, A., & Wemelsfelder, F. (2008). The qualitative assessment of responsiveness to environmental challenge in horses and ponies. Appl. Anim. Behav. Sci., 109(2-4), 342–354.
Abstract: The responsiveness of 10 horses and 10 ponies to environmental challenge (represented by an open field test) was assessed using a qualitative approach based on free choice profiling methodology (FCP), which gives observers complete freedom to choose their own descriptive terms. Data were analysed with generalised Procrustes analysis (GPA), a multivariate statistical technique associated with FCP. A cross-validation of the outcomes of this approach to data recorded through quantitative behaviour analysis, and through a questionnaire given to the animals' owner/riding instructor, was also performed using principal component analysis (PCA). Twelve undergraduate students generated their own descriptive vocabularies, by watching 20 horse/pony video clips lasting 2.5 min each. GPA showed that the consensus profile explained a high percentage of variation among the 12 observers, and differed significantly from the mean randomised profile (p < 0.001). Two main dimensions of the consensus profile were identified, explaining 60% and 5.2% of the variation between animals, respectively. The 12 observer word charts interpreting these dimensions were semantically consistent, as they all converged towards the same meaning, albeit using different terms. The most used term to describe the positive end of axis 1 was “quiet”, whereas “attentive” was the best positive descriptor of axis 2. The most frequently used descriptors for the negative ends of axes 1 and 2 were “nervous” and “bored”, respectively. Thus, axis 1 was labelled as “quiet/nervous” and axis 2 was named as “attentive/bored”. A marked effect of animal category was observed on the scores of the animals on the first dimension (p < 0.001). Horses received significantly higher scores, and were thus assessed as more quiet and calm, than ponies. Conversely, ponies tended to receive lower scores on the second dimension (p < 0.12), therefore they appeared less curious and attentive. The results of the PCA showed that the variables from different types of measurement clearly had meaningful relationships. For instance, the variables with the highest loading on the positive end of axis 1 were all indicative of tractable and docile animals, whereas axis 2 showed high loadings on the positive end for variables indicating attentive animals. Qualitative behaviour assessment proved to be an appropriate methodology for the study of horse behavioural responsiveness, in that it provided a multifaceted characterisation of horse behavioural expression that was in agreement with other quantitative and subjective assessments of the animals' behaviour.
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Lansade, L., Pichard, G., & Leconte, M. (2008). Sensory sensitivities: Components of a horse's temperament dimension. Appl. Anim. Behav. Sci., 114(3-4), 534–553.
Abstract: Temperament is an important factor when working with horses. Behavioural tests have already been developed to measure certain dimensions of a horse's temperament (fearfulness, gregariousness, etc.). In order to measure the temperament more precisely, our work aimed to identify a dimension which has already been described in several species but not yet in horses, namely sensory sensitivity. Our study was based on the definition of a temperament dimension as “a behavioural characteristic stable across situations and over time”. We designed several tests for each sense and then determined whether the responses observed were correlated between situations and in time. The principle of the tests was to generate two stimuli of different intensities for each sense (e.g. two different sounds) and to measure the intensity of the horse's response (N = 26). Using Spearman rank correlations, we tested whether the responses to these different stimuli were inter-correlated. We repeated the same tests 5 months later to determine whether the responses were correlated over time. Within each sense, results show that the greater the horses' response to one stimulus, the greater their response to the other. For example, the reaction to the odour of cinnamon (time spent near the source of the odour) was significantly correlated to the reaction to lavender (R = 0.53, p = 0.004). The reactions to two different sounds or to two different tactile stimuli (von Frey filaments, or contact of a brush on the body), were also significantly correlated (R = 0.59, p < 0.0001; R = 0.38, p = 0.029). Finally, the reactions to two different tastes or to two visual stimuli tended to be correlated (R = 0.27, p = 0.09; R = 0.27, p = 0.09). However, there was no significant correlation between the responses to stimuli relating to different senses. Finally, except for the responses to odour, the responses to other sensory stimuli showed stability over a 5-month period (e.g. tactile stimulation: R = 0.71, p < 0.0001). In conclusion, our study revealed characteristics which were stable across situations and over time. The absence of links between the characteristics measured for the different senses suggests that a dimension for each sense exists (e.g. tactile sensitivity) rather than a general sensory sensitivity dimension covering all the senses.
Keywords: Horse; Equus caballus; Temperament; Sensory sensitivity; Behavioural tests
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Bertolucci, C., Giannetto, C., Fazio, F., & Piccione, G. (2008). Seasonal variations in daily rhythms of activity in athletic horses. Animal, 2(07), 1055–1060.
Abstract: Circadian rhythms reflect extensive programming of biological activity that meets and exploits the challenges and opportunities offered by the periodic nature of the environment. In the present investigation, we recorded the total activity of athletic horses kept at four different times of the year (vernal equinox, summer solstice, autumn equinox and winter solstice), to evaluate the presence of seasonal variations of daily activity rhythms. Athletic Thoroughbred horses were kept in individual boxes with paddock. Digitally integrated measure of total activity of each mare was continuously recorded by actigraphy-based data loggers. Horse total activities were not evenly distributed over the day, but they were mainly diurnal during the year. Daily activity rhythms showed clear seasonal variations, with the highest daily amount of activity during the vernal equinox and the lowest during the winter solstice. Interestingly, the amount of activity during either photophase or scotophase changed significantly throughout the year. Circadian analysis of horse activities showed that the acrophase, the estimated time at which the peak of the rhythm occurs, did not change during the year, it always occurred in the middle of the photoperiod. Analysing the time structure of long-term and continuously measured activity and feeding could be a useful method to critically evaluate athletic horse management systems in which spontaneous locomotor activity and feeding are severely limited. Circadian rhythms are present in several elements of sensory motor and psychomotor functions and these would be taken into consideration to plan the training schedules and competitions in athletic horses.
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Fraser, N. O., Schino, G., & Aureli, F. F. (2008). Components of Relationship Quality in Chimpanzees. Ethology, 114(9), 834–843.
Abstract: A novel approach to studying social relationships in captive adult chimpanzees (Pan troglodytes) was taken by using principal components analysis (PCA) to extract three key components of relationship quality from nine behavioural variables. Based on the loadings of the behavioural variables, the components appeared to match previously hypothesized critical aspects of social relationships and were therefore labelled Value, Compatibility and Security. The effects of kinship, sex combination, age difference and time spent together on each of the relationship quality components were analysed. As expected, kin were found to have more valuable, compatible and secure relationships than non-kin. Female2013female dyads were found to be more compatible than male2013male or mixed-sex dyads, whereas the latter were found to be most secure. Partners of a similar age were found to have more secure and more valuable relationships than those with a larger age gap. Individuals that were together in the group for longer were more valuable and more compatible, but their relationships were found to be less secure than individuals that were together in the group for a shorter time. Although some of the results may be unexpected based on chimpanzee socio-ecology, they fit well overall with the history and social dynamics of the study group. The methods used confer a significant advantage in producing quantitative composite measures of each component of relationship quality, obtained in an objective manner. These findings therefore promote the use of such measures in future studies requiring an assessment of the qualities of dyadic social relationships.
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Fabbri-Destro, M., & Rizzolatti, G. (2008). Mirror Neurons and Mirror Systems in Monkeys and Humans. Physiology, 23(3), 171–179.
Abstract: Mirror neurons are a distinct class of neurons that transform specific sensory information into a motor format. Mirror neurons have been originally discovered in the premotor and parietal cortex of the monkey. Subsequent neurophysiological (TMS, EEG, MEG) and brain imaging studies have shown that a mirror mechanism is also present in humans. According to its anatomical locations, mirror mechanism plays a role in action and intention understanding, imitation, speech, and emotion feeling.
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King, A. J., Douglas, C. M. S., Huchard, E., Isaac, N. J. B., & Cowlishaw, G. (2008). Dominance and affiliation mediate despotism in a social primate. Curr Biol, 18(23), 1833–1838.
Abstract: Group-living animals routinely have to reach a consensus decision and choose between mutually exclusive actions in order to coordinate their activities and benefit from sociality. Theoretical models predict “democratic” rather than “despotic” decisions to be widespread in social vertebrates, because they result in lower “consensus costs”-the costs of an individual foregoing its optimal action to comply with the decision-for the group as a whole. Yet, quantification of consensus costs is entirely lacking, and empirical observations provide strong support for the occurrence of both democratic and despotic decisions in nature. We conducted a foraging experiment on a wild social primate (chacma baboons, Papio ursinus) in order to gain new insights into despotic group decision making. The results show that group foraging decisions were consistently led by the individual who acquired the greatest benefits from those decisions, namely the dominant male. Subordinate group members followed the leader despite considerable consensus costs. Follower behavior was mediated by social ties to the leader, and where these ties were weaker, group fission was more likely to occur. Our findings highlight the importance of leader incentives and social relationships in group decision-making processes and the emergence of despotism.
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Rands, S. A., Cowlishaw, G., Pettifor, R. A., Rowcliffe, J. M., & Johnstone, R. A. (2008). The emergence of leaders and followers in foraging pairs when the qualities of individuals differ. BMC Evol Biol, 8, 51.
Abstract: BACKGROUND: Foraging in groups offers animals a number of advantages, such as increasing their likelihood of finding food or detecting and avoiding predators. In order for a group to remain together, there has to be some degree of coordination of behaviour and movement between its members (which may in some cases be initiated by a decision-making leader, and in other cases may emerge as an underlying property of the group). For example, behavioural synchronisation is a phenomenon where animals within a group initiate and then continue to conduct identical behaviours, and has been characterised for a wide range of species. We examine how a pair of animals should behave using a state-dependent approach, and ask what conditions are likely to lead to behavioural synchronisation occurring, and whether one of the individuals is more likely to act as a leader. RESULTS: The model we describe considers how the energetic gain, metabolic requirements and predation risks faced by the individuals affect measures of their energetic state and behaviour (such as the degree of behavioural synchronisation seen within the pair, and the value to an individual of knowing the energetic state of its colleague). We explore how predictable changes in these measures are in response to changes in physiological requirements and predation risk. We also consider how these measures should change when the members of the pair are not identical in their metabolic requirements or their susceptibility to predation. We find that many of the changes seen in these measures are complex, especially when asymmetries exist between the members of the pair. CONCLUSION: Analyses are presented that demonstrate that, although these general patterns are robust, care needs to be taken when considering the effects of individual differences, as the relationship between individual differences and the resulting qualitative changes in behaviour may be complex. We discuss how these results are related to experimental observations, and how the model and its predictions could be extended.
Keywords: Animals; *Feeding Behavior; *Food Chain; *Models, Biological; *Social Dominance
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Hoffmann, & G. (2008). Bewegungsaktivität und Stressbelastung bei Pferden in Auslaufhaltungssystemen mit verschiedenen Bewegungsangeboten.
Abstract: Pferdehaltungssysteme mit angrenzenden Ausläufen gelten als eine sehr tiergerechte
Haltungsform, da sie den Tieren eine gewisse Bewegungsmöglichkeit bieten. Ziel der vorliegenden Untersuchung war es, zu erfassen, ob der angrenzende Auslauf selbst einen ausreichenden Anreiz zur Bewegung darstellt und wie sich verschiedene Bewegungs- und Platzangebote auf die Bewegungsaktivität von Pferden in einer Gruppen-Auslaufhaltung auswirken. Zudem wurde ermittelt, welche Auswirkung die Bewegungsform bzw. –intensität auf das Wohlbefinden der Tiere hat. Der Großteil der in Deutschland gehaltenen Pferde verbringt die meiste Zeit des Tages im Stall, obwohl mittlerweile bekannt ist, dass Pferde unter natürlichen Haltungsbedingungen 12 bis 16 Stunden des Tages in Bewegung verbringen. Der Optimierung der Stallhaltungssysteme gilt daher ein besonderes Interesse. Zu diesem Zweck wurden von September 2004 bis Oktober 2005 Versuche mit 24 Warmblutstuten im Alter von 1½ bis 3½ Jahren in Einzel- und Gruppen- Auslaufhaltungssystemen durchgeführt. Jeweils sechs Pferde bildeten eine Versuchsgruppe. In jeder Gruppe fanden fünf Varianten von einer ca. dreiwöchigen Dauer statt. Die Gruppenhaltung wurde dabei durch drei unterschiedliche Zusatzbewegungsangebote (2 Std. Weide / Tag, 2 Std. unbegrünte Koppel / Tag, 1 Std. Freilauf- Führanlage / Tag) ergänzt. In der Einzel-Auslaufhaltung (Box mit 45 m²-großem angrenzenden Auslauf) und in einer Versuchsvariante der Gruppenhaltung bekamen die Pferde hingegen keine zusätzliche Bewegung außerhalb des Stallhaltungssystems angeboten. Das Gruppenhaltungssystem selbst war durch die räumliche Trennung der Funktionsbereiche (Liegen, Fressen, Trinken, Bewegen) gekennzeichnet und der angrenzende Auslauf war 270 m² groß. In einer zusätzlichen Versuchsphase fand in der Gruppenhaltung eine Erweiterung des permanent zugänglichen Auslaufs auf insg. 540 m² statt. Die Bewegungsaktivität wurde mit Pedometern erfasst, die an jeweils einem Hinterbein der Pferde befestigt wurden und ergänzend fand eine Analyse von Videoaufzeichnungen statt. Zur Beurteilung der Stressbelastung fanden Messungen der Herz192 Zusammenfassung frequenzvariabilität (Parameter HF und SD2) und der fäkalen Cortisolmetabolitenkonzentration statt. Die Auswertung des Bewegungsverhaltens ergab, dass eine zusätzliche zweistündige freie Bewegung der Pferdegruppe auf einer Weide zu einer deutlichen Steigerung der durchschnittlichen Bewegungsaktivität (149,6 Min. / Tag) führt, ebenso wie eine einstündige Bewegung in einer Führanlage (173,0 Min. / Tag). Eine unbegrünte Koppel regte die Pferde der Gruppenhaltung hingegen nicht zu vermehrter Bewegung an (131,6 Min. / Tag), sondern bewirkte z. T. sogar eine Abnahme der Bewegungsaktivität. In der Gruppen-Auslaufhaltung ohne zusätzliches Bewegungsangebot war die Bewegungsaktivität ebenfalls gering (125,8 Min / Tag) und während der Einzel-Auslaufhaltung ohne Zusatzbewegung zeigten die Pferde die geringste Bewegungsaktivität (102,3 Min. / Tag). Bei der alleinigen Analyse der Bewegungszeit im Stallhaltungssystem war kein signifikanter Einfluss der zusätzlichen Bewegung außerhalb des Stallsystems auf die übrige Fortbewegung feststellbar. Auch eine Vergrößerung des an den Stall angrenzenden Auslaufs im Gruppenhaltungssystem hatte keinen steigernden Einfluss auf das Bewegungsverhalten der Pferde. Die Stressbelastung der Pferde war in den Varianten der Gruppenhaltung mit zweistündigem Weidegang (SD2: 82,9 ms; Cortisolmetaboliten: 29,0 nmol / kg Kot) sowie der einstündigen Bewegung in einer Freilauf-Führanlage (SD2: 99,2 ms; Cortisolmetaboliten: 27,7 nmol / kg Kot) am geringsten. Die Untersuchungen zeigten eine Stresszunahme in der Gruppenhaltung mit zweistündigem Auslauf auf einer unbegrünten Koppel ohne Futterangebot (SD2: 101,3 ms; Cortisolmetaboliten: 39,6 nmol / kg Kot) sowie in der Variante der Gruppenhaltung ohne zusätzliches Bewegungsangebot (SD2: 113,3 ms; Cortisolmetaboliten: 38,4 nmol / kg Kot). Dem Mittelwert der Gruppe nach zu folgern hatten die Pferde während der Einzelhaltung ohne Zusatzbewegung eine sehr große Stressbelastung (SD2: 123,8 ms; Cortisolmetaboliten: 37,5 nmol / kg Kot). Ein Vergleich der Gruppen- und Einzelhaltung hinsichtlich der Herzfrequenzvariabilität hat jedoch gezeigt, dass insg. 70 % der Pferde während der Haltung in einer Gruppe weniger Stress empfinden. Es gab aber auch Zusammenfassung 193 Pferde (30 %), die in der Einzelhaltung eine abnehmende Stressbelastung zeigten, wobei hier der Einfluss der Rangordnung eine entscheidende Rolle zu spielen scheint. Durch die Auswertung mehrerer Messparameter (sowohl für Stress- als auch für Bewegungsverhalten) werden gleichgerichtete Tendenzen bei den Versuchsvarianten deutlich, allerdings ist eine eindeutige Gewichtung der Parameter nicht möglich. Somit ist die methodische Vorgehensweise dieser Untersuchung sehr positiv und als notwendig anzusehen, da die Messdaten auch immer gewissen Schwankungen durch externe Einflüsse unterliegen. Allgemein ist festzuhalten, dass Auslaufhaltungssysteme zwar eine gewisse Anregung zur Bewegung bieten, aber mit maximal vier Stunden (insg. 62 – 248 Min.) Bewegung pro Tag war der tägliche Anteil an Bewegung sehr viel geringer als beispielsweise bei Pferden in freier Wildbahn oder ganzjähriger Weidehaltung. Somit deckt ein Auslaufhaltungssystem trotz getrennter Funktionsbereiche und eines großen Auslaufs nicht den Bewegungsbedarf der Pferde, wenn keine zusätzlichen Bewegungsanreize und –möglichkeiten angeboten werden. Eine zusätzliche Bewegung von Pferden ist nicht nur zur Gesunderhaltung des Bewegungsapparates und der Körperfunktionen notwendig, sondern auch um das Wohlbefinden und die Ausgeglichenheit der Pferde zu steigern. [Horse husbandry systems with close-by discharge are considered to be a very livestock- friendly housing form, as they offer a certain movement opportunity for the animals. The aim of the present study was to examine how different movement and space offerings affect the movement activities of horses in a group horse husbandry with close-by discharge, and whether the discharge provides itself an adequate incentive for movement. The impact that the form or rather intensity of movement has on the wellbeing of the animals was also established. Most of the horses held in Germany spend most of the day in the stable, although it is meanwhile known that horses under natural housing conditions are 12 to 16 hours of the day in motion. Therefore the improvement of stable housing systems applies a special interest. For this purpose, 24 warmblood mares, aged from 1½ to 3½ years, were studied in single and group discharge husbandry systems from September 2004 until October 2005. Six horses formed an experimental group. In every group five variants of approximately three weeks were proceeded. Thereby the group husbandry was supplemented with three different additional movement opportunities (2 h pasture / day, 2 h non-grassy pasture land / day, 1 h free range horse walker / day). In the single discharge husbandry (single box with 45 sq. m-large close-by discharge) and in one experimental variant of the group husbandry got the horses, however, offered no additional movement outside the husbandry system. The group husbandry system itself was marked by the spatial division of the functional areas (lying, eating, drinking, moving) and the close-by discharge measured 270 sq. m. In an additional phase of the study, and expansion of the permanently accessible close-by discharge to 540 sq. m was found. The movement activity was documented with pedometers attached respectively to one hind leg of the horse and a supplementary analysis of video documentation. To evaluate the stress exposure measurements of heart frequency variability (parameters HF and SD2) and of the faecal cortisol metabolite concentration were performed. Summary 195 The interpretation of the movement behaviour showed that additional two hours of free movement on a pasture led to a significant increase in the average movement activity (149.6 min / day), as well as one hour movement in a horsewalker did (173.0 min / day). The non-grassy pasture land, however, didn’t inspire the horses of the group husbandry to increased movement (131.6 min / day), but sometimes even caused a decrease in movement activity. In the group discharge husbandry without additional movement opportunities the movement activity was also low (125.8 min / day), and during the single discharge husbandry without additional movement the horses showed the least movement activity (102.3 min / day). In analysing only the movement time in the stable system was no significant impact of the additional movement outside the housing system to the rest of locomotion ascertainable. As well an expansion of the close-by stable discharge in the group husbandry system had no increasing influence on the movement behaviour of the horses. The stress exposure of the horses was least in the variations of group husbandry with two hours on a pasture (SD2: 82.9 ms; cortisol metabolites: 29.0 nmol / kg faeces) as well as one hour of movement in a free range horse walker (SD2: 99.2 ms; cortisol metabolites: 27.7 nmol / kg faeces). The studies showed a rise in stress in group husbandry with two hours of movement on a non-grassy pasture land without feeding opportunity (SD2: 101.3 ms; cortisol metabolites: 39.6 nmol / kg faeces) as well as in the variation of the group husbandry without additional movement offerings (SD2: 113.3 ms; cortisol metabolites: 38.4 nmol / kg faeces). Judging from the mean of the group the horses had a very high stress exposure in the variation of the single husbandry without additional movement offerings (SD2: 123.8 ms; cortisol metabolites: 37.5 nmol / kg faeces). But a comparison of the group and single husbandry in terms of the heart frequency variability showed that alltogether 70 % of the horses experienced less stress if hold in a group. However, some horses (30 %) showed reducing stress in the single husbandry, whereas here the influence of social hierarchy seems to play a decisive role. 196 Summary In consequence of the examination of several measuring parameters (both for stressand for movement behaviour) parallel aligned tendencies become apparent in the experimental variants, however, is a unique weighting of the parameters not possible. Thus, the methodological approach of this study is to be regarde as very positive and necessary, since the data always vary with some fluctuations by external influences. In general it can be established that discharge husbandry systems offer some incentive for the horse to move, but with a maximum of four hours (overall 62 – 248 min) of movement per day, the daily proportion of movement was much less than, for example, in the case of wild horses or year-round pasture keeping. Thus, if no additional movement incentives and possibilities are offered, the discharge husbandry system doesn’t cover the movement needs of the horse despite separate functional areas and a large outside discharge. Additional movement is not only necessary to keep the musculoskeletal system and bodily functions of the horse healthy, but also to ensure the horse’s well being and mental balance.] |
Langbein, J., Siebert, K., & Nuernberg, G. (2008). Concurrent recall of serially learned visual discrimination problems in dwarf goats (Capra hircus). Behav Proc, 79. |
Dugnol, B., Fernández, C., Galiano, G., & Velasco, J. (2008). On a chirplet transform-based method applied to separating and counting wolf howls. Signal Process, 88. |