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Smuts Gl,. (1975). Home range sizes for Burchell's Zebra, Equus burchelli antiquorum from the Krüger National Park. Koedoe, 18, 139–146.
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Smuts Gl,. (1975). Pre – and postnatal growth phenomena of Burchell's Zebra, Equus Burchelli Antiquorum. Koedoe, 18, 69–102.
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Sivak, J. G., & Allen, D. B. (1975). An evaluation of the “ramp” retina of the horse eye. Vision Res, 15(12), 1353–1356.
Abstract: Using a rapid freezing and sectioning technique, the distance between the lens and retina of the horse eye was measured. There is no indication of a ramp retina that could serve accommodation. The pupil axis of the eye coincides with the maximum lens to retina distance. The changes in the lens-retina distance are greater below the axis than above it. Calculations were made of refractive power of the horse eye from measurements of curvature and refractive indices of the ocular tissues. These calculations agree both qualitatively and quantitatively with retinoscopic measurements on live horses. Both show that the refractive state shifts in the direction of hyperopia above and below the axis and that this shift is greater below the axis than above it. Some dynamic accommodative ability in the living eye was observed.
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Short Rv,. (1975). The evolution of the horse. J Reprod Fert Suppl, 23, 1–6.
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Schmoldt, A., Benthe, H. F., & Haberland, G. (1975). Digitoxin metabolism by rat liver microsomes. Biochem Pharmacol, 24(17), 1639–1641.
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Scherer, W. F., Madalengoitia, J., Flores, W., & Acosta, M. (1975). Ecologic studies of Venezuelan encephalitis virus in Peru during 1970-1971. Am J Epidemiol, 101(4), 347–355.
Abstract: Venezuelan encephalitis (VE) virus has intermittently produced epidemics and equine epizootics on the dry Pacific coastal plain of Peru since at least the 1930's. However, evidence that the virus exists in the Amazon region of Peru to the east of the Andes mountains was not obtained until antibodies were found in human sera collected in 1965, and 10 strains of the virus were isolated in a forest near the city of Iquitos, Peru during February and March 1971. Eight strains came from mosquitoes and two from dead sentinel hamsters. Three hamsters exposed in forests near Iquitos developed VE virus antibodies suggesting that hamster-benign strains also exist there. Antibody tests of equine sera revealed no evidence that VE virus was actively cycling during the late 1950's or 1960's in southern coastal Peru, where equine epizootics had occurred in the 1930's and 1940's. In northern coastal Peru bordering Ecuador, antibodies were present in equine sera, presumably residual from the 1969 outbreak caused by subtype I virus, since neutralizing antibody titers were higher to subtype I virus than to subtypes III or IV. No VE virus was detected in this northern region during the dry season of 1970 by use of sentinel hamsters. The possibility is considered that VE epidemics and equine epizootics on the Pacific coast of Peru are caused by movements of virus in infected vertebrates traversing Andean passes or in infected vertebrates or mosquitoes carried in airplanes from the Amazon region.
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Ruckebusch Y,. (1975). The hypnogram as an index of adaptation of farm animals to changes in their environment. App Anim Ethol, 2, 3–18.
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Rossdale Pd,. (1975). Das Pferd, Fortpflanzung und Entwicklung. Karger 1975, .
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Pickett Bw, V. J. (1975). Abnormalities of mating behaviour in domestic stallions. J Reprod Fert Suppl, 23, 129–134.
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Owaga Ml,. (1975). The feeding ecology of wildbeest and zebra in Athi – Kaputei plains. E Afr Wildl J, 13, 375–384.
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