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Niekerk Van Ch, A. W. (1975). Early embryonic development in the horse. J Reprod Fert Suppl, 23, 495–498.
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Penzhorn Bl,. (1985). Reproductive characteristics of a free – ranging population of Cape mountin zebra. J Reprod Fert, 73, 51–57.
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Penzhorn Bl, L. P. (1987). Comparisons of reproductive parameters of two Cape mountain zebra populations. J Reprod Fert Suppl, 35, 661–663.
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Penzhorn, B. L., & van der Merwe, N. J. (1988). Testis size and onset of spermatogenesis in Cape mountain zebras (Equus zebra zebra). J Reprod Fert, 83, 371–375.
Abstract: Testis mass of adult Cape mountain zebra stallions (mean 70·0 g) was appreciably less than that of other zebra species and domestic horses. The histological appearance of the testes of 11-, 24- and 29-month-old colts was typically prepubertal. Spermatogenic activity of a 4-year-old stallion obtained at the end of summer was at a very low level, while a 4·5-year-old stallion obtained 6 weeks after the winter solstice showed a marked increase in spermatogenesis compared with the 4-year-old. Stallions 6·5-19 years of age collected in different seasons all showed active spermatogenesis.
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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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Rossdale Pd, S. R. (1967). The time of foaling of thoroughbred mares. J Reprod Fert, 13, 342–343.
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Schwarzenberger, F., Mostl, E., Bamberg, E., Pammer, J., & Schmehlik, O. (1991). Concentrations of progestagens and oestrogens in the faeces of pregnant Lipizzan, trotter and thoroughbred mares. J Reprod Fertil Suppl, 44, 489–499.
Abstract: Faecal samples were collected at weekly intervals from pregnant Lipizzan mares during Weeks 7-16 following mating and from Lipizzan, Trotter and Thoroughbred mares during the last 3 months of gestation. After parturition, samples were taken daily from the Thoroughbred mares for another 6 days. Non-pregnant mares served as controls. The concentrations of unconjugated oestrogens (Eg), 20 alpha-OH-progestagens (20 alpha-G) and 20 beta-OH-progestagens (20 beta-G) were measured by enzyme immunoassay. In the faeces of Lipizzan mares, immunoreactive progestagens were significantly (P less than 0.01) elevated above the levels in non-pregnant mares by Week 11, and Eg by Week 13 of pregnancy onwards. During the last 3 months of gestation, concentrations of Eg were significantly higher in Trotter mares than in Lipizzan and Thoroughbred mares. Concentrations of 20 alpha-G and 20 beta-G increased to maximal values in the last month of gestation. There was no significant difference among the 3 breeds with respect to 20 alpha-G but, during the 10 weeks before parturition, concentrations of 20 beta-G in the Lipizzan mares were significantly lower (P less than 0.05) than those in the Thoroughbred mares. They were also significantly lower than those of the Trotter mares during the last 4 weeks of gestation. After parturition, the concentrations of Eg and progestagens had declined to baseline values by Days 3 and 4 respectively. From these results we conclude that high concentrations of progestagens with 20 alpha- and 20 beta-hydroxyl groups are present in the faeces of pregnant mares, especially during the last month of gestation.
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Short Rv,. (1975). The evolution of the horse. J Reprod Fert Suppl, 23, 1–6.
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SUMMERS PM et al,. (1987). Sucessful transfer of the embryos of Przewalski's horses and Grant's zebra to domestic mares. J Reprod Fert, 80, 13–20.
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Turner, J. W. J., & Kirkpatrick, J. F. (1982). Androgens, behaviour and fertility control in feral stallions. J Reprod Fertil Suppl, 32, 79–87.
Abstract: This field study of feral stallions in Montana and Idaho examines and correlates the seasonal pattern of plasma androgens and specific sociosexual behaviour and reports the effect of a long-acting androgenic steroid on this behaviour and on fertility. Plasma testosterone was measured by competitive protein binding assay in samples obtained by jugular venepuncture from captured animals. In samples taken from 34 sexually mature stallions in 6 different months during the year, a definite seasonal pattern in testosterone was present, with a peak in May (3.04 +/- 0.63 ng/ml) and a nadir in December (1.55 +/- 0.34 ng/ml). Values were less than 2.0 ng/ml in non-breeding months and greater than 2.4 ng/ml in breeding months. Behavioural endpoints measured were (1) stallion scent marking in response to elimination by mares (elimination marking), (2) mounting and (3) copulation. The frequencies of each of these endpoints followed closely the seasonal pattern seen for plasma androgens. In the fertility study microcapsulated testosterone propionate (microTP) was administered i.m. to 10 harem stud stallions 3 months before the 1980 breeding season. In these stallions and in 10 control harem studs, the above behavioural endpoints were examined in the 1980 and 1981 breeding seasons, and foal counts were made in 1981. There were no direct inhibitory or stimulatory effects of microTP treatment on any of the behavioural endpoints in either year. In 1981 foals were produced in 87.5% of the control bands and 28.4% of the microTP-treated bands. These results indicate that microencapsulated testosterone propionate can provide effective fertility control in feral horses without causing significant alterations in sociosexual behaviour.
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