|
|
Giraldeau, L. - A., Lefebvre, L., & Morand-Ferron, J. (2007). Can a restrictive definition lead to biases and tautologies? Behav. Brain Sci., 30(4), 411–412.
Abstract: We argue that the operational definition proposed by Ramsey et al. does not represent a significant improvement for students of innovation, because it is so restrictive that it might actually prevent the testing of hypotheses on the relationships between innovation, ecology, evolution, culture, and intelligence. To avoid tautological thinking, we need to use an operational definition that is taxonomically unbiased and neutral with respect to the hypotheses to be tested.
|
|
|
|
Wotschikowsky, U. (2007). Wölfe und Jäger in der Oberlausitz. Broschüre, Freundeskreis freilebender Wölfe, .
|
|
|
|
Versace, E., Morgante, M., Pulina, G., & Vallortigara, G. (2007). Behavioural lateralization in sheep (Ovis aries). Behav. Brain. Res., 184(1), 72–80.
Abstract: This study investigates behavioural lateralization in sheep and lambs of different ages. A flock was tested in a task in which the animals were facing an obstacle and should avoid it on either the right or left side to rejoin flock-mates (adult sheep) or their mothers (lambs). A bias for avoiding the obstacle on the right side was observed, with lambs apparently being more lateralized than sheep. This right bias was tentatively associated with the left-hemifield laterality in familiar faces recognition which has been documented in this species. Differences between adult sheep and lambs were likely to be due to differences in social reinstatement motivation elicited by different stimuli (flock-mates or mothers) at different ages. Preferential use of the forelegs to step on a wood-board and direction of jaw movement during rumination was also tested in adult animals. No population bias nor individual-level lateralization was observed for use of the forelegs. At the same time, however, there was a large number of animals showing individual-level lateralization for the direction of jaw movement during rumination even though there was no population bias. These findings highlight that within the same species individual- and population-level lateralization can be observed in different tasks. Moreover, the results fit the general hypothesis that population-level asymmetries are more likely to occur in tasks that require social coordination among behaviourally asymmetric individuals.
|
|
|
|
Zentall, T. R. (2006). Imitation: definitions, evidence, and mechanisms. Anim. Cogn., 9(4), 335–353.
Abstract: Imitation can be defined as the copying of behavior. To a biologist, interest in imitation is focused on its adaptive value for the survival of the organism, but to a psychologist, the mechanisms responsible for imitation are the most interesting. For psychologists, the most important cases of imitation are those that involve demonstrated behavior that the imitator cannot see when it performs the behavior (e.g., scratching one's head). Such examples of imitation are sometimes referred to as opaque imitation because they are difficult to account for without positing cognitive mechanisms, such as perspective taking, that most animals have not been acknowledged to have. The present review first identifies various forms of social influence and social learning that do not qualify as opaque imitation, including species-typical mechanisms (e.g., mimicry and contagion), motivational mechanisms (e.g., social facilitation, incentive motivation, transfer of fear), attentional mechanisms (e.g., local enhancement, stimulus enhancement), imprinting, following, observational conditioning, and learning how the environment works (affordance learning). It then presents evidence for different forms of opaque imitation in animals, and identifies characteristics of human imitation that have been proposed to distinguish it from animal imitation. Finally, it examines the role played in opaque imitation by demonstrator reinforcement and observer motivation. Although accounts of imitation have been proposed that vary in their level of analysis from neural to cognitive, at present no theory of imitation appears to be adequate to account for the varied results that have been found.
|
|
|
|
van Heel, M. C. V., Kroekenstoel, A. M., van Dierendonck, M. C., van Weeren, P. R., & Back, W. (2006). Uneven feet in a foal may develop as a consequence of lateral grazing behaviour induced by conformational traits. Equine. Vet. J., 38(7), 646–651.
Abstract: REASONS FOR PERFORMING STUDY: Conformational traits are important in breeding, since they may be indicative for performance ability and susceptibility to injuries. OBJECTIVES: To study whether certain desired conformational traits of foals are related to lateralised behaviour while foraging and to the development of uneven feet. METHODS: Twenty-four Warmblood foals, born and raised at the same location, were studied for a year. Foraging behaviour was observed by means of weekly 10 min scan-sampling for 8 h. A preference test (PT) was developed to serve as a standardised tool to determine laterality. The foals were evaluated at age 3, 15, 27 and 55 weeks. The PT and distal limb conformation were used to study the relation between overall body conformation, laterality and the development of uneven feet. Pressure measurements were used to determine the loading patterns under the feet. RESULTS: About 50% of the foals developed a significant preference to protract the same limb systematically while grazing, which resulted in uneven feet and subsequently uneven loading patterns. Foals with relatively long limbs and small heads were predisposed to develop laterality and, consequently unevenness. CONCLUSIONS: Conformational traits may stimulate the development of laterality and therefore indirectly cause uneven feet.
|
|
|
|
Gomez Alvarez, C. B., Rhodin, M., Bobber, M. F., Meyer, H., Weishaupt, M. A., Johnston, C., et al. (2006). The effect of head and neck position on the thoracolumbar kinematics in the unridden horse. Equine Vet J Suppl, (36), 445–451.
Abstract: REASONS FOR PERFORMING STUDY: In many equestrian activities a specific position of head and/or neck is required that is dissimilar to the natural position. There is controversy about the effects of these positions on locomotion pattern, but few quantitative data are available. OBJECTIVES: To quantify the effects of 5 different head and neck positions on thoracolumbar kinematics of the horse. METHODS: Kinematics of 7 high level dressage horses were measured walking and trotting on an instrumented treadmill with the head and neck in the following positions: HNP2 = neck raised, bridge of the nose in front of the vertical; HNP3 = as HNP2 with bridge of the nose behind the vertical; HNP4 = head and neck lowered, nose behind the vertical; HNP5 = head and neck in extreme high position; HNP6 = head and neck forward and downward. HNP1 was a speed-matched control (head and neck unrestrained). RESULTS: The head and neck positions affected only the flexion-extension motion. The positions in which the neck was extended (HNP2, 3, 5) increased extension in the anterior thoracic region, but increased flexion in the posterior thoracic and lumbar region. For HNP4 the pattern was the opposite. Positions 2, 3 and 5 reduced the flexion-extension range of motion (ROM) while HNP4 increased it. HNP5 was the only position that negatively affected intravertebral pattern symmetry and reduced hindlimb protraction. The stride length was significantly reduced at walk in positions 2, 3, 4 and 5. CONCLUSIONS: There is a significant influence of head/neck position on back kinematics. Elevated head and neck induce extension in the thoracic region and flexion in the lumbar region; besides reducing the sagittal range of motion. Lowered head and neck produces the opposite. A very high position of the head and neck seems to disturb normal kinematics. POTENTIAL RELEVANCE: This study provides quantitative data on the effect of head/neck positions on thoracolumbar motion and may help in discussions on the ethical acceptability of some training methods.
|
|
|
|
Weishaupt, M. A., Wiestner, T., von Peinen, K., Waldern, N., Roepstorff, L., van Weeren, R., et al. (2006). Effect of head and neck position on vertical ground reaction forces and interlimb coordination in the dressage horse ridden at walk and trot on a treadmill. Equine Vet J Suppl, (36), 387–392.
Abstract: REASONS FOR PERFORMING STUDY: Little is known in quantitative terms about the influence of different head-neck positions (HNPs) on the loading pattern of the locomotor apparatus. Therefore it is difficult to predict whether a specific riding technique is beneficial for the horse or if it may increase the risk for injury. OBJECTIVE: To improve the understanding of forelimb-hindlimb balance and its underlying temporal changes in relation to different head and neck positions. METHODS: Vertical ground reaction force and time parameters of each limb were measured in 7 high level dressage horses while being ridden at walk and trot on an instrumented treadmill in 6 predetermined HNPs: HNP1 – free, unrestrained with loose reins; HNP2 – neck raised, bridge of the nose in front of the vertical; HNP3 – neck raised, bridge of the nose behind the vertical; HNP4 – neck lowered and flexed, bridge of the nose considerably behind the vertical; HNP5 – neck extremely elevated and bridge of the nose considerably in front of the vertical; HNP6 – neck and head extended forward and downward. Positions were judged by a qualified dressage judge. HNPs were assessed by comparing the data to a velocity-matched reference HNP (HNP2). Differences were tested using paired t test or Wilcoxon signed rank test (P<0.05). RESULTS: At the walk, stride duration and overreach distance increased in HNP1, but decreased in HNP3 and HNP5. Stride impulse was shifted to the forehand in HNP1 and HNP6, but shifted to the hindquarters in HNP5. At the trot, stride duration increased in HNP4 and HNP5. Overreach distance was shorter in HNP4. Stride impulse shifted to the hindquarters in HNP5. In HNP1 peak forces decreased in the forelimbs; in HNP5 peak forces increased in fore- and hindlimbs. CONCLUSIONS: HNP5 had the biggest impact on limb timing and load distribution and behaved inversely to HNP1 and HNP6. Shortening of forelimb stance duration in HNP5 increased peak forces although the percentage of stride impulse carried by the forelimbs decreased. POTENTIAL RELEVANCE: An extremely high HNP affects functionality much more than an extremely low neck.
|
|
|
|
Leiner, L. (2006). Vergleich verschiedener Methoden zur Angstextinktion bei Pferden. Diploma thesis, , .
Abstract: Pferde sind Fluchttiere. Ihr Fluchtinstinkt bewirkt, dass sie sich leicht erschrecken und auch in
diversen Situationen mit Flucht reagieren. Diese Tatsache ist den meisten Reitern bekannt,
nur ist es für den Menschen teilweise schwer, mit dieser Eigenschaft auszukommen und sie zu
verstehen oder gar nachzuvollziehen. So kommt es häufig zu Unfällen, die aus der Angst der
Pferde resultieren, jedoch vermeidbar gewesen wären, hätte man ankündigende Signale früher
erkannt. Des Weiteren kann die Angst eines Pferdes auch durch eine (Ver-) Weigerung,
bestimmte Dinge zu tun, sichtbar werden. Diese Weigerung wird in der Reiterei gerne als
„Bockigkeit“ und „Ungehorsam“ des Pferdes interpretiert und führt nicht selten zu einer
Bestrafung. Insgesamt kann man sagen, dass angstauslösende Reize und die Reaktionen des
Pferdes darauf oft falsch eingeschätzt oder falsch interpretiert werden und in der Folge auch
falsch damit umgegangen wird. Ein Grund dafür ist sicher das fehlende Wissen über das
Verhalten des Pferdes. Mit der vorliegenden Diplomarbeit soll ein Beitrag geleistet werden,
das Pferd in seinem Angstverhalten besser zu verstehen. Ziel der Arbeit war es, das Verhalten
des Pferdes bei verschiedenen Intensitäten von Angst zu untersuchen. Des Weiteren wurden
Methoden untersucht, mit denen man die Angst von Pferden vor bestimmten Reizen und
Situationen potentiell lindern kann, was letztendlich auch der Unfallvorbeugung dient.
Die vorliegende Diplomarbeit wurde am Haupt- und Landesgestüt Marbach durchgeführt; 24
Junghengste standen hierfür zur Verfügung. Darunter waren 18 Deutsche Warmblüter, 3
Vollblutaraber und 3 Schwarzwälder Füchse (Kaltblüter), somit war auch ein Rassenvergleich
möglich.
In einem ersten Teil der Arbeit wurde untersucht, wie sich Angst bei Pferden äußert. Hierfür
wurde ausgenutzt, dass Pferde ganz generell vor unbekannten, neuen Gegenständen Angst
haben (= Neophobie). Zur Angstauslösung dienten als Konfrontationsgegenstände ein
Sonnenschirm und eine Plastikplane. Beide Gegenstände waren für die Testpferde unbekannt.
Das Verhalten sowie die Herzrate der Tiere wurden während aller Versuche beobachtet und
quantifiziert. Nacheiner ersten Konfrontation wurden die Pferde an die Objekte gewöhnt
(Extinktionstraining = Angstlöschung) und beobachtet welche Verhaltensymptome sich
während dieser Gewöhnung (= Verlust der Neophobie) verändern. Die Hypothese war, dass
tatsächliche Angstsymptome während der Gewöhnung immer seltener zu beobachten sind.
Zusammenfassung III
Als Verhaltensweisen für Angst konnten Ausweichbewegungen und Flucht, Lautäußerungen
(Prusten und Schnauben), das Anspannen der Halsmuskulatur sowie das Vordrücken der
Oberlippe identifiziert werden. Darüber hinaus wurde gezeigt, dass Abstufungen im
Angstverhalten möglich sind: Bei sehr hohem Angstlevel sind Fluchtreaktionen zu
beobachten. Bei mittlerem Angstlevel treten Ausweichbewegungen im Schritt und
Lautäußerungen (Prusten und Schnauben) auf, bei geringem Angstlevel wird die
Halsmuskulatur angespannt und die Oberlippe vorgedrückt.
Im Zweiten Teil der Arbeit sollten verschiedene Methoden zur Angst-Extinktionauf ihre
Wirksamkeit hin untersucht werden. Verwendet wurde in verschiedenen Testgruppen die
Methode der Desensibilisierung (d.h. leichte, schrittweise stärker werdende Exposition
gegenüber dem angstauslösenden Reiz), die Desensibilisierung mit Gegenkonditionierung
(positive Verstärkung) durch Streicheln bzw. Reiben des Halses und die Desensibilisierung
mit Gegenkonditionierung durch Futterbelohnung. Als Kontrollgruppe dienten Pferde, die
ohne eine Konfrontation mit dem angstauslösenden Reiz nur über den Versuchplatz geführt
wurden.
Während des Extinktionstrainings konnte beobachtet werden, dass die Desensibilisierung mit
Gegenkonditionierung zu einer schnelleren Extinktion führt als ohne Gegenkonditionierung.
Allerdings zeigte ein Vergleich mit der Kontrollgruppe, die das Extinktionstraining nicht
erfahren hatte, den gleichen Verlust an Angstverhalten wie die Gruppen mit Extinktionstraining.
Dieses Ergebnis wurde so interpretiert, dass die wiederholte Exposition gegenüber
angstauslösenden Reizen bei den durchgeführten Verhaltenstests zwar eine Rolle spielt, doch
dass auch allein die Beschäftigung mit den Tieren zu einem Verlust von Angstverhalten führt
(wahrscheinlich auch aufgrund eines wachsenden Vertrauens zur Führperson, die über das
komplette Experiment hin die Gleiche blieb).
|
|
|
|
Fagot, J., & Cook, R. G. (2006). Evidence for large long-term memory capacities in baboons and pigeons and its implications for learning and the evolution of cognition. Proc Natl Acad Sci U S A, 103.
|
|
|
|
Lim, M. M., & Young, L. J. (2006). Neuropeptidergic regulation of affiliative behavior and social bonding in animals. Hormon. Behav., 50(4), 506–517.
Abstract: Social relationships are essential for maintaining human mental health, yet little is known about the brain mechanisms involved in the development and maintenance of social bonds. Animal models are powerful tools for investigating the neurobiological mechanisms regulating the cognitive processes leading to the development of social relationships and for potentially extending our understanding of the human condition. In this review, we discuss the roles of the neuropeptides oxytocin and vasopressin in the regulation of social bonding as well as related social behaviors which culminate in the formation of social relationships in animal models. The formation of social bonds is a hierarchical process involving social motivation and approach, the processing of social stimuli and formation of social memories, and the social attachment itself. Oxytocin and vasopressin have been implicated in each of these processes. Specifically, these peptides facilitate social affiliation and parental nurturing behavior, are essential for social recognition in rodents, and are involved in the formation of selective mother-infant bonds in sheep and pair bonds in monogamous voles. The convergence of evidence from these animal studies makes oxytocin and vasopressin attractive candidates for the neural modulation of human social relationships as well as potential therapeutic targets for the treatment of psychiatric disorders associated with disruptions in social behavior, including autism.
|
|
