|
|
Hunt, G. R., Gray R.D., & Taylor, A. H. (2013). Why is tool use rare in animals? (Boesch C C. J. anz C, Ed.). Cambridge, MA.: Cambridge University Press.
|
|
|
|
Sighieri, C., Tedeschi, D., De Andreis, C., Petri, L., & Baragli, P. (2003). Behaviour Patterns of Horses Can be Used to Establish a Dominant-Subordinate Relationship Between Man and Horse. Animal Welfare, 12(4), 705–708.
Abstract: This paper describes how man can enter the social hierarchy of the horse by mimicking the behaviour and stance it uses to establish dominance. A herd is organised according to a dominance hierarchy established by means of ritualised conflict. Dominance relationships are formed through these confrontations: one horse gains the dominant role and others identify themselves as subordinates. This study was conducted using five females of the Haflinger breed, totally unaccustomed to human contact, from a free-range breeding farm. The study methods were based on the three elements fundamental to the equilibrium of the herd: flight, herd instinct and hierarchy. The trainer-horse relationship was established in three phases: retreat, approach and association. At the end of the training sessions, all of the horses were able to respond correctly to the trainer. These observations suggest that it is possible to manage unhandled horses without coercion by mimicking their behaviour patterns.
|
|
|
|
Rehren, K. D. (2018). Untersuchung der „Schiefe“ des Pferdes:Symmetrie von Bewegungsablauf und Hufbelastung (Bernhard Ohnesorge Harald Sieme P. S. Karsten Feige, Ed.). Ph.D. thesis, Cuvillier Verlag, Göttingen.
Abstract: 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.
|
|
|
|
Reinhardt, I., Kluth, G., Balzer, S., & Steyer, K. (2022). Wolfsverursachte Schäden, Präventions- und Ausgleichszahlungen in Deutschland 2021 (Markus Ritz, Ed.) (Vol. 41). Görlitz, Deutschland: DBBW-Dokumentations- und Beratungsstelle des Bundes zum Thema Wolf.
|
|
|
|
Wallner, B., Palmieri, N., Vogl, C., Rigler, D., Bozlak, E., Druml, T., et al. (2017). Y Chromosome Uncovers the Recent Oriental Origin of Modern Stallions. Current Biology, 27(13), 2029–2035.e5.
Abstract: The Y chromosome directly reflects male genealogies, but the extremely low Y chromosome sequence diversity in horses has prevented the reconstruction of stallion genealogies [1, 2]. Here, we resolve the first Y chromosome genealogy of modern horses by screening 1.46 Mb of the male-specific region of the Y chromosome (MSY) in 52 horses from 21 breeds. Based on highly accurate pedigree data, we estimated the de novo mutation rate of the horse MSY and showed that various modern horse Y chromosome lineages split much later than the domestication of the species. Apart from few private northern European haplotypes, all modern horse breeds clustered together in a roughly 700-year-old haplogroup that was transmitted to Europe by the import of Oriental stallions. The Oriental horse group consisted of two major subclades: the Original Arabian lineage and the Turkoman horse lineage. We show that the English Thoroughbred MSY was derived from the Turkoman lineage and that English Thoroughbred sires are largely responsible for the predominance of this haplotype in modern horses.
|
|
|
|
Reinhardt, I., Kluth, G., Nowak, C., Szentiks, C. A., Krone, O., Ansorge, H., et al. (2019). Military training areas facilitate the recolonization of wolves in Germany. Conservation Letters, 12(3), e12635.
Abstract: Abstract Wolves (Canis lupus) are currently showing a remarkable comeback in the highly fragmented cultural landscapes of Germany. We here show that wolf numbers increased exponentially between 2000 and 2015 with an annual increase of about 36%. We demonstrate that the first territories in each newly colonized region were established over long distances from the nearest known reproducing pack on active military training areas (MTAs). We show that MTAs, rather than protected areas, served as stepping-stones for the recolonization of Germany facilitating subsequent spreading of wolf territories in the surrounding landscape. We did not find any significant difference between MTAs and protected areas with regard to habitat. One possible reason for the importance of MTAs may be their lower anthropogenic mortality rates compared to protected and other areas. To our knowledge, this is the first documented case where MTAs facilitate the recolonization of an endangered species across large areas.
|
|
|
|
López-Bao, J. V., Sazatornil, V., Llaneza, L., & Rodríguez, A. (2013). Indirect Effects on Heathland Conservation and Wolf Persistence of Contradictory Policies that Threaten Traditional Free-Ranging Horse Husbandry. Conservation Letters, 6(6), 448–455.
Abstract: Abstract Conservation agencies within the European Union promote the restoration of traditional land uses as a cost-effective way to preserve biodiversity outside reserves. Although the European Union pursues the integration of the environment into strategic decision-making, it also dictates sectoral policies that may damage farmland biodiversity. We illustrate this point by outlining the socioeconomic factors that allow the persistence of traditional free-ranging horse husbandry in Galicia, northwestern Spain. Free-ranging Galician mountain ponies provide ecological and socioeconomic services including the prevention of forest fires, the maintenance of heathlands and wolves, and the attenuation of wolf-human conflicts. This traditional livestock system may have persisted because it entails negligible costs for farmers. Wolf predation upon Galician mountain ponies does not threaten farmer's economies and seems to be tolerated better than attacks to more valuable stock. Recently, European Union's regulations on animal welfare, carcass management, or meat production put new economic and administrative burdens on farmers, make free-ranging horse rearing economically unsustainable, and incentivize its abandonment. The aim of the European Union to integrate environmental policies may be successful to preserve farmland biodiversity only through careful anticipation of the side effects of apparently unrelated regulations on the fragile equilibrium that sustain traditional land uses.
|
|
|
|
Burton, A. C., Neilson, E., Moreira, D., Ladle, A., Steenweg, R., Fisher, J. T., et al. (2015). REVIEW: Wildlife camera trapping: a review and recommendations for linking surveys to ecological processes. J Appl Ecol, 52(3), 675–685.
Abstract: Summary Reliable assessment of animal populations is a long-standing challenge in wildlife ecology. Technological advances have led to widespread adoption of camera traps (CTs) to survey wildlife distribution, abundance and behaviour. As for any wildlife survey method, camera trapping must contend with sources of sampling error such as imperfect detection. Early applications focused on density estimation of naturally marked species, but there is growing interest in broad-scale CT surveys of unmarked populations and communities. Nevertheless, inferences based on detection indices are controversial, and the suitability of alternatives such as occupancy estimation is debatable. We reviewed 266 CT studies published between 2008 and 2013. We recorded study objectives and methodologies, evaluating the consistency of CT protocols and sampling designs, the extent to which CT surveys considered sampling error, and the linkages between analytical assumptions and species ecology. Nearly two-thirds of studies surveyed more than one species, and a majority used response variables that ignored imperfect detection (e.g. presence?absence, relative abundance). Many studies used opportunistic sampling and did not explicitly report details of sampling design and camera deployment that could affect conclusions. Most studies estimating density used capture?recapture methods on marked species, with spatially explicit methods becoming more prominent. Few studies estimated density for unmarked species, focusing instead on occupancy modelling or measures of relative abundance. While occupancy studies estimated detectability, most did not explicitly define key components of the modelling framework (e.g. a site) or discuss potential violations of model assumptions (e.g. site closure). Studies using relative abundance relied on assumptions of equal detectability, and most did not explicitly define expected relationships between measured responses and underlying ecological processes (e.g. animal abundance and movement). Synthesis and applications. The rapid adoption of camera traps represents an exciting transition in wildlife survey methodology. We remain optimistic about the technology's promise, but call for more explicit consideration of underlying processes of animal abundance, movement and detection by cameras, including more thorough reporting of methodological details and assumptions. Such transparency will facilitate efforts to evaluate and improve the reliability of camera trap surveys, ultimately leading to stronger inferences and helping to meet modern needs for effective ecological inquiry and biodiversity monitoring.
|
|
|
|
Heydebreck, K. von. (1928). Reitlehrer und Reiter in Uniform und Zivil eine Anleitung nach den Grundsätzen der deutschen Reitvorschrift (2., neubearb. Aufl ed.). Berlin: Mittler.
|
|
|
|
Krueger, K., Gruentjens, T., & Hempel, E. (2023). Wolf contact in horses at permanent pasture in Germany. Plos One, 18(8), e0289767.
Abstract: Wolves returned to Germany in 2000, leading to fear in German horse owners that their horses could be in danger of wolf attacks or panic-like escapes from pastures when sighting wolves. However, reports from southern European countries indicate that wolf predation on horses diminishes with increasing presence of wildlife. Therefore, we conducted a long-term, filed observation between January 2015 and July 2022 on 13 non breeding riding horses, mares and geldings, kept permanently on two pastures within the range of wildlife and a stable wolf pack with annual offspring. Wildlife cameras at the fences of the pastures made 984 times recordings of wolves and 3151 times recordings of wildlife in and around the pastures. Between 1 January 2022 and 23 March 2022 we observed two stable horse groups. Pasture 1 was grazed by five horses of mixed breed, four mares and one gelding, with the median age of 8 years (min. = 6y, max. = 29y). Pasture 2 was grazed by eight heavy warmbloods and draught horses, three mares and five geldings, with the median age of 16 years (min. = 13y, max. = 22y). During this period no wolf was recorded at pasture 2, but wild boar several times, whereas at pasture 1, wolves were recorded 89 times, and for the wildlife mostly hare. Wolves may have avoided pasture 2 because of the presence of wild boar or because the large group of older, heavy breed horses may have formed a stable, protective group. The latter needs to be confirmed in a follow-up field observation, which records anti-predator behavior and welfare indicators in horses. In conclusion, wolves did not attack the mature horses on pastures with plenty of wildlife and the horses did not respond to the presence of wolves with visible signs of reduced welfare or panic. This indicates that wolves may prefer to prey on easily accessible wildlife around and at horse pastures and that Central European horses become accustom to the presence of non-hunting wolves.
|
|
