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Huebener, E. (2005). Hilfen für Übergänge von einer Gangart in eine andere ? Die Bewegungen von Pferderumpf und -rücken als Zeitgeber für reiterliche Einwirkung. Trakehner Hefte,, 5-11.
Abstract: Übergänge von einer Gangart in eine andere sind nach Ludwig Koch jeweils nur aus einer ganz bestimmten Phase einer Bewegungsfolge (oder Bewegungsfolgen-Hälfte) der einen in eine ganz bestimmte Bewegungsfolge (oder Bewegungsfolgen-Hälfte) der anderen Gangart möglich.
Diese Phasen dauern nur Bruchteile einer Sekunde an. In diesen Momenten muß die Hilfe nach europäischer klassischer Lehre gegeben, nur in diesen Momenten kann sie vom Pferd blitzartig-automatisch umgesetzt werden. Um die Hilfe im “passenden” Moment geben zu können, braucht der Reiter einen Zeitgeber. Den einzigen verfügbaren, zuverlässigen Timer bilden die Bewegungen des Pferderückens und des Pferderumpfes.
Die Zusammenhänge zwischen den Bewegungsphasen in den Grundgangarten, dem mit frei beweglichem Beckenring allen Bewegungen des Pferderückens folgendem Sitz des Reiters, und dem Schenkel, der von Schritt zu Schritt, von Tritt zu Tritt, von Galoppsprung zu Galoppsprung an den wegschwingenden Pferderumpf fallen möchte bis er das im rechten Augenblick – vom Reiter gesteuert – dann auch darf, sind erstmals in piktogrammartigen Miniaturbild-Folgen leicht verständlich dargestellt.
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Huebener, E. (2005). Das Sitzrätsel lösen (Arbeitstitel: So kann der Reiter wirklich “sitzen”!);. Mecl. Pf.erde J., 3, 50–51.
Abstract: Zusammenfassung
Die Bewegungen des Pferderückens und des Pferderumpfes sind aus den Fußfolgen der Grundgangarten ableitbar. Damit gewinnt Sitzschulung ein solides Fundament. Die entscheidenden Merkmale dieser Bewegungen sind hier erläutert.
Einige überwiegend altbekannte Grundlagen der Sitzschulung werden bewertet. Was sich aus neueren Erkenntnissen zu den Bewegungen des Pferderückens und des Pferderumpfes für den Sitz des Reiters ergibt, ist in drei Punkten leichtverständlich erklärt. Prinzipdarstellungen unterstützten dies.
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Huebener, E. (2005). Der Natur abgelauschte Erkenntnisse: Der Weg zum Balancesitz und zum Begreifen des Timers für Signale an das Pferd;. Tierärztl. Umschau, 2, 90–99.
Abstract: Zusammenfassung
Mit dem Beitrag “Die Bewegungen von Pferderumpf und -rücken aus der Sicht des Reiters” (TU 59, 327-334, 2004) wurde um universitäre Forschung zur Ermittlung gemessener Werte für diese Begleiter der Fortbewegung geworben.
Die Entdeckung des Ranges der Rumpf-Rücken-Bewegungen für pferdgerechtes und kultiviertes, feinfühliges Reiten ist mit der Entwicklung des Balancesitzes und der Technik des vom Pferd Zeitvorgaben Empfangens und ihm Signale Sendens (Reiter sagen: des Fühlens und Einwirkens) eng verbunden. Ihre Geschichte läßt sich über viereinhalb Jahrhunderte verfolgen. Ein kurzer Abriß wird hier nachgeliefert.
Er mündet erneut in ein Plädoyer für interdisziplinäres universitäres Forschen, weil auch bei Sitz und Hilfengebung, weiteren Grundlagen des Reitens – im Interesse effektiveren Unterrichts an der Basis unseres “Sports” – dringender Klärungsbedarf besteht.
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Judge, P. G., & Mullen, S. H. (2005). Quadratic postconflict affiliation among bystanders in a hamadryas baboon group. Anim. Behav., 69(6), 1345–1355.
Abstract: The tendency in primate groups for two opponents to affiliate shortly after a fight has been described as dyadic reconciliation. The response has been shown to restore disrupted relationships and curtail ongoing aggression. Rates of self-directed behaviour (e.g. scratching) are positively correlated with anxiety in primates and the rates decline after reconciliation, indicating that the response also functions to reduce postconflict tension. Third parties not involved in an aggressive interaction are also likely to affiliate with one of the combatants subsequent to a fight. Such `triadic' interactions may also promote conflict resolution when, for instance, the relatives of a victim affiliate with their relative's aggressor. Because aggression in a group influences a bystander's behaviour with combatants, we hypothesized that aggression between two animals would also influence a bystander's behaviour with other bystanders. Such `quadratic' postconflict interactions might also function to reduce postconflict tension or occur in patterns among kin subgroups to resolve conflict. We tested for quadratic interactions in an 18-member group of captive hamadryas baboons, Papio hamadryas hamadryas. Immediately following a fight, an uninvolved bystander was randomly selected for observation and its affiliative interactions with other bystanders and its displacement activities were recorded for 3 min. Rates of behaviour during these postconflict periods were compared to rates during 3-min baseline periods not preceded by aggression. Bystanders engaged in quadratic interactions by increasing affiliation with other bystanders following aggression. Bystanders directed affiliation to nonkin bystanders that were their preferred social partners. Displacement activities of bystanders were significantly higher during postconflict intervals compared to baseline intervals, and bystander displacement activity levels before affiliative contact with other bystanders were significantly higher than after contact. Apparently, bystanders become tense or anxious after witnessing aggression and affiliate with preferred partners to reduce the arousal.
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Earley, R. L., Druen, M., & Alan Dugatkin, L. (2005). Watching fights does not alter a bystander's response towards naive conspecifics in male green swordtail fish, Xiphophorus helleri. Anim. Behav., 69(5), 1139–1145.
Abstract: Bystanders are capable of extracting cues from signalling interactions between others and appear to use information gained via eavesdropping when confronted with the watched individuals. A question that has gained little attention is whether observing fights affects bystander behaviour outside the context of interacting with the watched individuals. Our aim was to determine whether watching fights elicits general changes in bystander aggression levels in Xiphophorus helleri. We manipulated the bystanders' ability to witness encounters using clear, one-way-mirror and opaque partitions. After watching (or not watching) an initial contest, the bystanders were pitted against naive conspecifics instead of the animals they had seen fight. Observing fights did not alter the bystanders' propensity to initiate aggression, escalate, or win against naive individuals, indicating that bystanders do not experience general changes in aggressive behaviour after watching a fight. Earlier work in this species, however, has shown that bystanders respond in predictable ways to individuals they have witnessed winning or losing a fight. Taken together, these data support the notion that bystanders consistently modify their behaviour towards previously watched winners or losers in response to information gained via eavesdropping. We discuss our results in light of some recent work on the behavioural and endocrinological responses triggered by watching fights and suggest that comparative approaches to understanding networking phenomena may be productive.
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Shettleworth, S. J., & Sutton, J. E. (2005). Multiple systems for spatial learning: dead reckoning and beacon homing in rats. J Exp Psychol Anim Behav Process, 31(2), 125–141.
Abstract: Rats homed with food in a large lighted arena. Without visual cues, they used dead reckoning. When a beacon indicated the home, rats could also use the beacon. Homing did not differ in 2 groups of rats, 1 provided with the beacon and 1 without it; tests without the beacon gave no evidence that beacon learning overshadowed dead reckoning (Experiment 1). When the beacon was at the home for 1 group and in random locations for another, there was again no evidence of cue competition (Experiment 2). Dead reckoning experience did not block acquisition of beacon homing (Experiment 3). Beacon learning and dead reckoning do not compete for predictive value but acquire information in parallel and are used hierarchically.
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Skov-Rackette, S. I., & Shettleworth, S. J. (2005). What do rats learn about the geometry of object arrays? Tests with exploratory behavior. J Exp Psychol Anim Behav Process, 31(2), 142–154.
Abstract: Six experiments using habituation of exploratory behavior tested whether disoriented rats foraging in a large arena encode the shapes of arrays of objects. Rats did not respond to changes in position of a single object, but they responded to a change in object color and to a change in position of 1 object in a square array, as in previous research (e.g., C. Thinus-Blanc et al., 1987). Rats also responded to an expansion of a square array, suggesting that they encoded sets of interobject distances rather than overall shape. In Experiments 4-6, rats did not respond to changes in sense of a triangular array that maintained interobject distances and angles. Shapes of object arrays are encoded differently from shapes of enclosures.
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Gibson, B. M., & Shettleworth, S. J. (2005). Place versus response learning revisited: tests of blocking on the radial maze. Behav Neurosci, 119(2), 567–586.
Abstract: Neurobiological and behavioral research indicates that place learning and response learning occur simultaneously, in parallel. Such findings seem to conflict with theories of associative learning in which different cues compete for learning. The authors conducted place+response training on a radial maze and then tested place learning and response learning separately by reconfiguring the maze in various ways. Consistent with the effects of manipulating place and response systems in the brain (M. G. Packard & J. L. McGaugh, 1996), well-trained rats showed strong place learning and strong response learning. Three experiments using associative blocking paradigms indicated that prior response learning interferes with place learning. Blocking and related tests can be used to better understand how memory systems interact during learning.
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Shettleworth, S. J. (2005). Taking the best for learning. Behav. Process., 69(2), 147–9; author reply 159–63.
Abstract: Examples of how animals learn when multiple, sometimes redundant, cues are present provide further examples not considered by Hutchinson and Gigerenzer that seem to fit the principle of taking the best. “The best” may the most valid cue in the present circumstances; evolution may also produce species-specific biases to use the most functionally relevant cues.
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Sutton, J. E., & Shettleworth, S. J. (2005). Internal sense of direction and landmark use in pigeons (Columba livia). J Comp Psychol, 119(3), 273–284.
Abstract: The relative importance of an internal sense of direction based on inertial cues and landmark piloting for small-scale navigation by White King pigeons (Columba livia) was investigated in an arena search task. Two groups of pigeons differed in whether they had access to visual cues outside the arena. In Experiment 1, pigeons were given experience with 2 different entrances and all pigeons transferred accurate searching to novel entrances. Explicit disorientation before entering did not affect accuracy. In Experiments 2-4, landmarks and inertial cues were put in conflict or tested 1 at a time. Pigeons tended to follow the landmarks in a conflict situation but could use an internal sense of direction to search when landmarks were unavailable.
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