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Malcom Jr, L. H. (1975). Notes on wild dogs hunting zebras. Mammalia, 39, 231–240.
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Eisenmann V,. (1975). Nouvelles interpretations des restes d`équides de Nihowan Equus teilhardi Nov.Sp. Geobios, 8, 125–134.
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Jensen, G. D., Gordon, B. N., & Wolfheim, J. (1975). Nursing behavior in infant monkeys: a sequence analysis. Behaviour, 55(1-2), 115–127.
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Mitchell, D., & Allen, W. R. (1975). Observations on reproductive performance in the yearling mare. J. Reprod. Fert.,, (Suppl. 23), 531–536.
Abstract: Reproductive performance was studied in 137 yearling mares run with stallions in small groups for 3 months between June and August in 1968 to 1971 (four breeding seasons). Pregnancy diagnosis by repeated rectal palpation and qualitative tests for PMSG, showed that ninety-five mares conceived of which forty-four aborted spontaneously between days 30 and 160 of gestation. Laboratory examination of twenty-one aborted fetuses failed to show any infectious agents. Serial quantitative and qualitative tests for PMSG in aborting animals gave results similar to those observed in mares with normal pregnancies. Plasma progestagen assays showed marked individual variations although the loss of the conceptus was always associated with a drop in progestagen level. The high incidence of early pregnancy loss in these pubertal mares may also be related to immaturity, inadequate nutrition and physical stress.
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Welsh Da,. (1975). Population, behavioural, and grazing ecology of the Sable Island, Nova Scotia. Ph.D. thesis, Dalhousie University, Halifax.
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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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Bannikov, A. G. (1975). Recent status of the wild ass in Mongolia. IUCN Bulletin, 6(4), 16.
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Feist, J. D., & McCullough, D. R. (1975). Reproduction in feral horses. J Reprod Fertil Suppl, (23), 13–18.
Abstract: A behavioural study of feral horses was conducted on the Pryor Mountain Wild Horse Range in the western United States. All 270 horses on the Range were identified individually. The sex ratio was nearly balanced. Foal to adult female ratio was 43-2:100. Morality was concentrated among foals and old horses. Horses were organized as forty-four harem groups each with a dominant stallion, one to two immature stallions, one to three immature mares, one to three adult mares and their yearling and foal offspring, and 23 bachelor groups of one to eight stallions. Harem groups were quite stable year-round because of dominance and leadership by the stallions and group fidelity by mares and their offsring. Most changes occurred during the breeding season and involved immature females. Defeat of dominant stallions was infrequent. Immature males were tolerated because of their submissive behaviour. Bachelor stallion groups were inherently unstable. Mares came into heat after foaling in May/June, and were mated by harem stallions only.
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Dunn, M. F., & Branlant, G. (1975). Roles of zinc ion and reduced coenzyme in horse liver alcohol dehydrogenase catalysis. The mechanism of aldehyde activation. Biochemistry, 14(14), 3176–3182.
Abstract: 1,4,5,6-Tetrahydronicotinamide adenine dinucleotide (H2NADH) has been investigated as a reduced coenzyme analog in the reaction between trans-4-N,N-dimethylaminocinnamaldehyde (I) (lambdamax 398 nm, epsilonmax 3.15 X 10-4 M-minus 1 cm-minus 1) and the horse liver alcohol dehydrogenase-NADH complex. These equilibrium binding and temperature-jump kinetic studies establish the following. (i) Substitution of H2NADH for NADH limits reaction to the reversible formation of a new chromophoric species, lambdamax 468 nm, epsilonmax 5.8 x 10-4 M-minus 1 cm-minus 1. This chromophore is demonstrated to be structurally analogous to the transient intermediate formed during the reaction of I with the enzyme-NADH complex [Dunn, M. F., and Hutchison, J. S. (1973), Biochemistry 12, 4882]. (ii) The process of intermediate formation with the enzyme-NADH complex is independent of pH over the range 6.13-10.54. Although studies were limited to the pH range 5.98-8.72, a similar pH independence appears to hold for the H2NADH system. (iii) Within the ternary complex, I is bound within van der Waal's contact distance of the coenzyme nicotinamide ring. (iv) Formation of the transient intermediate does not involve covalent modification of coenzyme. Based on these findings, we conclude that zinc ion has a Lewis acid function in facilitating the chemical activation of the aldehyde carbonyl for reduction, and that reduced coenzyme plays a noncovalent effector role in this substrate activating step.
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Zimen, E. (1975). Social dynamics of the wolf pack. In M. W. Fox (Ed.), The wild canids (pp. 336–362). New York: Van Nostrand Reinhold.
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