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Huebener, E. |
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Basis Seat and Leg Aids – Evolution of Knowledge |
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Reiten Lesen Denken @ eberhardhuebener @ |
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1763 |
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Hübener, Eberhard |
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Title |
Horse-Appropriate Aids And Their Timer |
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2007 |
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www.reiten-lesen-denken.de |
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Harmony between man and horse, and the rider`s understanding of the function of a horse`s body and mind – these are things that knowledgeable horsemen have demanded for centuries. Constant, focussed attention enables the horse to understand barely visible signals from its herd leader or its rider (!) and to act upon them instantly. Thus it is not necessary to treat a horse as if it were either unwilling or deaf.
When the rider sits in perfect balance, his leg tends to fall “self-actively” against the horse`s trunk as it swings away when the horse`s hind leg on the same side moves forwards. This is the only moment in which a horse is able to immediately follow the signal from the rider to move forwards, sideways, or to hold back. Video footage proves what we already knew more than a hundred years ago, but which our sports organisations have somehow managed to forget. Of course we should not let our leg fall against the horse all the time, because then the horse will not register this as a signal. It is explained how to “switch on” and “switch off” the leg signals.
For the equestrian standards in this country, it is essential that young riders are familiarized with the “self-active” leg, as soon as they are halfway firm in the saddle. Youngsters learn this easily and never forget it again; it is far more difficult for adults, as the pelvic ring is no longer so flexible. As there is a definite lack of good riding lessons, an instructive video on this subject would be extremely useful. Sponsors are urgently required!
For riders who have mastered the balanced seat and can feel how their leg falls against the horse`s trunk as it swings away, riding becomes primarily a matter of self discipline.
If we do not examine these matters scientifically, we are in danger of loosing the most important elements of the equestrian art. With this thought in mind, the author uses this essay to argue once again for interdisciplinary research of equitation at universities, and for the support of these projects by high ranking organisations. |
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Reiten Lesen Denken @ eberhardhuebener @ |
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Boitani, L. |
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Patterns of homesites attendance in two Minnesota wolf packs |
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1982 |
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Wolves of the World: Perspectives of Behavior, Ecology and Conservation |
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Noyes, Park Ridge |
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New York |
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Harrington, F.H.; Paquet, P.C. |
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Equine Behaviour @ team @ Boitani1982 |
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6474 |
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Zeeb K, |
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Verhaltensweisen beim Dülmener Primitivpferd. Hautpflege – Fortpflanzung – Erkunden und Meiden – Mimik und Ausdrucksbewegungen |
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1969 |
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Wissenschaftlicher Film C 986 Begleittext |
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from Professor Hans Klingels Equine Reference List |
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Rehren, K. D. |
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Untersuchung der „Schiefe“ des Pferdes:Symmetrie von Bewegungsablauf und Hufbelastung |
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2018 |
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Wissenschaftliche Reihe der Klinik für Pferde |
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Ziel der Studie war die Beschreibung der motorischen Lateralität („Schiefe“) gesunder adulter Pferde. Hierzu wurden 14 lahmfreie Pferde (10 Warmblüter, 4 Quarter Horses) auf dem Laufband in Schritt und Trab auf individuelle Abweichungen von der symmetri-schen Bewegung hinsichtlich Abstellung der Hinterhand, Wirbelsäulenform (Biegung), Vor- und Rückführung sowie Belastung von Vorder- und Hintergliedmaßen jeweils simul-tan hochfrequenzkinematographisch und kinetisch mittels resistiver Hufdrucksensoren untersucht. Zusätzlich wurden bevorzugte Abstellung und Biegung sowie Galopppräfe-renz klinisch bzw. reiterlich beurteilt, das Vorliegen einer Weideschrittpräferenz unter-sucht und Freilaufversuche (bevorzugte Abbiegerichtung, Ausweichrichtung um ein Hin-dernis, Galoppräferenz) durchgeführt. Keines der Pferde zeigte Symmetrie über alle Merkmale; zwar wurde bei jedem Merkmal für einzelne Probanden Symmetrie festgestellt, mit Ausnahme des Galopp-Freilaufver-suchs trat Asymmetrie jedoch häufiger auf. 12 Probanden zeigten in der Bewegungsana-lyse eine signifikante seitliche Abstellung (8x rechts (R), 4x links (L), mittlere seitliche Abweichung im Schritt 1,22°±1,09°, im Trab 1,05°±1,03°), 10 eine bevorzugte Biegung (9x L, 1x R), 13 signifikante Asymmetrien der Gliedmaßenvor- bzw. -rückführung und 12 eine signifikante asymmetrische Gliedmaßenbelastung für die normalisierte Spitzenkraft (PFN, peak force) bzw. den Impuls der Belastung (IN) an mindestens einem Beinpaar (alle Merkmale individuell wiederholbar). Linksabgestellte Pferde führten in beiden Gang-arten das rechte Hinterbein signifikant weiter zurück als nach rechts abgestellte Pferde, die tendenziell eher das linke Hinterbein weiter zurückführten. – Die auf dem Laufband festgestellten Asymmetrien traten in beiden Gangarten auf, aber nicht immer überein-stimmend, wobei die Richtung der bevorzugten Abstellung und ebenso der bevorzugten Biegung beim einzelnen Pferd in Schritt und Trab nie gegensätzlich waren. Jeder dieser beiden Parameter wurde daher für das einzelne Pferd über beide Gangarten zusammen-gefasst. Die Richtung von Abstellung und Biegung waren voneinander unabhängig, so-dass die Bewegungsmuster Abstellung ohne Biegung, Biegung ohne Abstellung, Abstel-lung mit Biegung in Laufrichtung (Travers) sowie Abstellung mit Biegung entgegen der Laufrichtung (Schulterherein) vorkamen. Kein Pferd war in beiden Merkmalen symmet-risch; für manche Pferde war neben der einfachen Biegung auch eine S-Form der Wir-belsäule signifikant. Die Belastungssymmetrie der Gliedmaßen war in beiden Gangarten von der Abstellung und der Biegung unabhängig, es gab aber Hinweise auf Zusammen-hänge zwischen bestimmten Kombinationen von Abstellung und Biegung einerseits und der Existenz einer Belastungsasymmetrie der Vorderbeine im Trab andererseits (unge-bogen mit Abstellung laufende und im Schulterherein laufende Pferde belasteten i.d.R. asymmetrisch).
8 Pferde wiesen eine signifikante Weideschrittpräferenz auf (5x L, 3x R), die bei ebenso vorhandener seitlicher Abstellung signifkant häufiger auf der der Abstellung abgewandten Seite auftrat. Sie wies keinen Zusammenhang mit der Rückführung der Hinterbeine im Schritt oder im Trab auf. Das Auftreten einer Weideschrittpräferenz war signifikant vom durch Abstellung und Biegung bestimmten Bewegungsmuster abhängig (Auftreten bei Abstellung ohne Biegung und bei Schulterherein, nicht bei Travers oder Biegung ohne Abstellung). Zudem zeigt die Präferenz der Pferde im Weideschritt eine starke Überein-stimmung mit der Belastungssymmetrie der Vorderbeine im Trab (bevorzugt vorgestelltes Bein wird mehr belastet (IN); symmetrische Belastung bei fehlender Präferenz). Im Hindernisversuch hatten 12 von 13 getesteten Probanden eine signifikant bevorzugte Ausweichrichtung (5x L, 7x R); diese war unabhängig von der gemessenen Wirbelsäulenform, lag aber bei Pferden mit seitlicher Abstellung überwiegend auf der Seite der gemessenen Abstellung. Im Abbiegeversuch zeigten 6 von 12 getesteten Probanden eine signifikant bevorzugte Abbiegerichtung (3x L, 3x R), diese war weder von der Abstellungsrichtung noch von der Wirbelsäulenform, der Weideschrittpräferenz oder der Belastungssymmetrie der Vorderbeine im Trab abhängig. Die meisten Pferde zeigten im Freilauf keine signifikante Galopppräferenz (2x L, 11x gerade (N), 1x R), wogegen reiterlich bei den meisten Pferden eine Präferenz festgestellt wurde; beide Beurteilungen stimmten ebenso wie die Beurteilungen verschiedener Reiter nicht miteinander überein. Die gemessene Abstellungsrichtung ließ sich durch visuelle Beobachtung mit hoher Si-cherheit vorhersagen. Die bevorzugte Wirbelsäulenform stimmte nicht mit der reiterlich oder an der Longe festgestellten Biegung überein, wohl aber mit der Seite, auf die die Mähne fällt. Die vorliegende Studie weist nach, dass individuell stabile motorische Lateralität, weitge-hend bestehend aus den den Merkmalen der reiterlich postulierten „Schiefe“, bei gesun-den Pferden in symmetrischen Gangarten besteht und dass zwischen bestimmten Merkmalen vorhersagbare Zusammenhänge bestehen. Daraus ergeben sich wertvolle Schlussfolgerungen für das reiterliche Geraderichten des Pferdes, für das in Übereinstimmung mit der Reitliteratur insbesondere die Lektion Schulterherein geeignet erscheint. Es ist gelungen, für die wesentlichen Merkmale Abstellung, Biegung und Belastungssymmetrie der Vordergliedmaßen im Trab klinische Tests aufzuzeigen, die mit hoher Sicher-heit die Ergebnisse der Bewegungsanalyse vorhersagen können, wobei Rückschlüsse auf weitere asymmetrische Merkmale möglich sind. Die reiterliche Beurteilung von bevor-zugter Biegung und Galopppräferenz scheint jedoch von weiteren Faktoren außer dem Pferd selbst abhängig zu sein und stimmt häufig nicht mit den messbaren Parametern überein. – In dieser Studie wird erstmals eine wissenschaftlich überprüfte und klinisch anwendbare Methode zur umfassenden Analyse der motorischen Lateralität im Sinne der „Schiefe“ eines Pferdes beschrieben.
Summary -“Crookedness“ in the Horse: Symmetry of Motion and Hoof Loading
The purpose of this study was description of motor laterality (in terms of “crookedness“) of sound adult horses. 14 non-lame horses (10 Warmblood horses, 4 Quarter Horses) were examined walking and trotting on a treadmill for individual motion asymmetry concerning keeping the hindlimbs at an angle (hindlimbs not tracking the frontlimbs, “hindquarter angle”), lateroflexion, pro- and retraction of the limbs as well as loading of front- and hindlimbs. High-speed-kinematography and resistive pressure sensors were used simultanously. The horses were also ridden to evaluate preferred lateroflexion and preferred lead in canter. Moving at an angle towards a preferred side was assessed visually. Laterality of grazing stance was tested, as well as preferred turning direction, obstacle avoidance direction and preferred lead in canter while moving unrestrained in an arena. None of the horses moved symetrically over all traits; although there were symmetrical traits with individual horses, asymmetry was more commen (except for the unrestrained preferred lead test). On the treadmill, 12 horses moved with their hindquarters significantly at a angle (8x right (R), 4x left (L), mean lateral angle 1,22°±1,09° at a walk and 1,05°±1,03° at a trot), 10 showed laterality for lateroflexion (9x L, 1x R), 13 had significant asymmetries for protraction and/ or retraction and 12 for loading of contralateral limbs concerning normalized peak force (PFN) and impulse (IN), respectively, of at least one pair of limbs (all with good repeatibility). Horses keeping their hindquarters to the left showed significantly larger retraction of the right hindlimb compared to horses keeping their hindquarters to the right, who tended to further retract the left hindlimb. – Asymmetries found on the treadmill occurred in both gaits but were not always the same in both gaits, though the direction of the hindquarter angle as well as that of the preferred lateroflexion never contradicted each other within the same individual. Therefore, a specific laterality direction of hindquarter angle and lateroflexion could be assigned to each horse. The direction of preferred hindquarter angle and lateroflexion, respectively, were independent of each other so that the movement patterns “hindquarter angle without lateroflexion”, “lateroflexion without hindquarter angle”, “hindquarter angle with lateroflexion to the same side” (hindquarter-in/ travers) and “hindquarter angle with lateroflexion to opposite sides” (shoulder-in) could be found; no horse moved symmetrical for both traits. The lateroflexion of some horses could even be regarded as a double bend. At both gaits, symmetry of limb loading was independent of hindquarter angle as well as lateroflexion, taken seperately; still, there seems to be a relation between certain combinations of hindquarter angle and lateroflexion, on the one side, and the existence or absence of asymmetric loading of the frontlimbs in trot (horses moving with hindquarter angle, but without lateroflexion, and horses moving in shoulder-in mostly had asymmetric frontlimb loading).
238 7. Summary8 horses displayed laterality for a grazing stance (5x L, 3x R); their hindquarter angle, if they showed one, was significantly more often on the opposite side of their advanced frontleg while grazing. The direction of the grazing stance was independent of hindlimb retraction symmetry in either gait. Occurrence of grazing stance laterality significantly depended on the movement pattern consisting of hindquarter angle and lateroflexion (horses moving with a hindquarter angle, but without lateroflexion, and horses moving in shoulder-in mostly showed grazing stance laterality, while horses moving with lateroflexion, but without a hindquarter angle, and horses moving in hindquarter-in did not). Also, grazing stance laterality was highly predictive of the symmetry of frontlimb loading at trot (advanced frontleg has significantly higher impulse (IN) at trot; horses without grazing stance laterality showed symmetrical impulse). 12 of 13 horses displayed laterality for obstacle avoidance direction (5x L, 7x R) that was independent of the individually preferred lateroflexion but if the horses showed a hindquarter angle it was usually to the same side. 6 of 12 horses showed laterality for turning direction (3x L, 3x R) that had no relation to laterality of either hindquarter angle, lateroflexion, grazing stance or frontlimb loading symmetry at trot. Most horses had no significant lead preference in the unrestrained canter test (2x L, 11x no preference (N), 1x R) even though riders assigned a lead preference to most horses; both ratings did not match, as well as the rating between two different riders did not match. The (measured) direction of hindquarter angle was highly predictable by visual asessment. Preferred (measured) lateroflexion did not match the direction of lateroflexion assigned by either rider or on the long line; it was in agreement with the mane side of the horse, though. This study proves that individual and stable motor laterality exists in sound horses in symmetrical gaits, mostly consisting of the traits that are hypothesized as “crookedness” in riding literature. It also shows that predictible relationships exist between certain traits thereof. This knowledge is valuable since it has implications for the training of riding horses for straightness, wherefore especially riding shoulder-in should be helpful. Relatively easy clinical tests could successfully be found that allow well predicting main features of individual horses ́ motor laterality like hindquarter angle, lateroflexion and frontlimb loading symmetry at trot as measured on the treadmill. Some conclusions can also be drawn for other asymmetrical traits. The asessment of preferred lateroflexion and canter lead performed by riders, though, seems to also underlie other influences than the horse itself and failed to be a predictor of the measured traits. – For the first time, a scientifically proven and clinically applicable method of asessing a horses motor laterality in terms of “crookedness” is presented. |
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http://dnb.d-nb.de |
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Ph.D. thesis |
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Cuvillier Verlag |
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Göttingen |
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Karsten Feige, Peter Stadler,Harald Sieme, Bernhard Ohnesorge |
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Equine Behaviour @ team @ |
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Vallortigara, G.; Chiandetti, C.; Sovrano, V.A. |
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Brain asymmetry (animal) |
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2011 |
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Wiley Interdisciplinary Reviews: Cognitive Science |
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WIREs Cogn Sci |
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2 |
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2 |
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146-157 |
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Once considered a uniquely human attribute, brain asymmetry has been proved to be ubiquitous among non-human animals. A synthetic review of evidence of animal lateralization in the motor, sensory, cognitive, and affective domains is provided, together with a discussion of its development and possible biological functions. It is argued that investigation of brain asymmetry in a comparative perspective may favor the link between classical neuropsychological studies and modern developmental and evolutionary biology approaches. WIREs Cogni Sci 2011 2 146–157 DOI: 10.1002/wcs.100 For further resources related to this article, please visit the WIREs website |
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John Wiley & Sons, Inc. |
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1939-5086 |
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Equine Behaviour @ team @ |
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5687 |
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Van Horik, J.; Emery, N. |
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Evolution of cognition |
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2011 |
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Wiley Interdiscip Rev Cogn Sci |
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Equine Behaviour @ team @ Van Horik2011 |
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6230 |
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Young, R.J. |
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Title |
Environmental Enrichment for Captive Animals |
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2003 |
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Wiley Interdiscip Rev Cogn Sci |
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Environmental enrichment is a simple and effective means of improving animal welfare in any species – companion, farm, laboratory and zoo. For many years, it has been a popular area of research, and has attracted the attention and concerns of animal keepers and carers, animal industry professionals, academics, students and pet owners all over the world. |
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6596 |
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Millspaugh, J.J.; Brundige, G.C.; Gitzen, R.A.; Raedeke, K.J. |
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Herd organization of cow elk in Custer State Park, South Dakota |
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Journal Article |
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2004 |
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Wildlife Society Bulletin |
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Wildl Soc Bull |
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32 |
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2 |
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506-514 |
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Cervus elaphus nelsoni, home range, kernel, Rocky Mountain Elk, social organization, subherd, utilization distribution, volume of intersection |
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nderstanding herd organization is important when considering management alternatives designed to benefit or manipulate elk (Cervus elaphus) populations. We studied the seasonal and annual herd organization of cow elk in Custer State Park, South Dakota from 1993-1997 by examining seasonal subherd range size, spatial arrangement, overlap, and site fidelity. Based on social interaction analyses, we combined locations of radiocol-lared cow elk to delineate subherds. We computed 95% kernel home ranges with least-squares cross validation for each subherd by season and year. Subherd overlap and fidelity by season and year were computed using the Volume of Intersection Index (VI) statistic. We identified 5 relatively discrete, resident cow-calf subherds. We observed little overlap in utilization distributions of adjacent subherds. The mean VI score across all subherds and time points (n=140) was 0.06 (SE=0.009), indicating an average 6% overlap in subherd area utilization. Subherd overlap between pairs was 0.08 in fall (SE= 0.021), 0.06 in winter (SE=0.018), 0.06 in spring (SE=0.2), and 0.05 in summer (SE= 0.016). Range sizes were not different between any pairs of seasons or years (F13,52=0.7, P=0.75). Subherd fidelity ranged from 0.41 (SE=0.033) to 0.60 (SE=0.018) overall, indicating differential use within the subherd boundary across years. The ability to distinguish discrete cow-calf subherd units is consistent with other studies and may aid elk management in Custer State Park. However, use patterns within subherd boundaries were inconsistent across years and may reflect human disturbances (e.g., hunting and logging activities), differences in our sampling approach, or changes in matriarchal leadership. Further evaluation into factors affecting space-use patterns is necessary to predict changes in range use within the subherd boundary. |
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Linklater, W.L.; Cameron, E.Z.; Minot, E.O.; Stafford, K.J. |
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Feral horse demography and population growth in the Kaimanawa Ranges, New Zealand |
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2004 |
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Wildl. Res. |
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2 |
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119-128 |
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Although feral horses are a common management problem in numerous countries, detailed and long-term demographic studies are rare. We measured the age and sex structure, and pregnancy, birth and death rates in a population of 413 feral horses in New Zealand during 1994–98 and used them to construct a model simulating population growth. Survivorship increased with age (0–1 years old = 86.8%, 1–2 = 92.3%, 2–4 = 92.4%, ≥? 4 years old = females 94%, males 97% per annum). Birth sex ratio parity, a slight female bias in the adult sex ratio (92 males per 100 females) and higher adult male survivorship indicated lower average survivorship for young males than females that was not detectable in mortality statistics. Pregnancy and foaling rates for mares ≥? 2 years old averaged 79 and 49%, respectively. Foaling rates increased as mares matured (2–3-year-old mares = 1.9%, 3–4 = 20.0%, 4–5 = 42.1%, ≥? 5 = 61.5% per annum). Young mares had higher rates of foetal and neonatal mortality (95% of pregnancies failed and/or were lost as neonatal foals in 2–3-year-old mares, 70.6% in 3–4, 43.2% in 4–5, and 31% in mares ≥? 5 years old). Population growth was 9.6% per annum (9.5–9.8, 95% CI) without human-induced mortalities (i.e. r = 0.092). Our model, standardised aerial counts, and historical estimates of annual reproduction suggest that the historical sequence of counts since 1979 has overestimated growth by ~50% probably because of improvements in count effort and technique.</p> |
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