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Reed-Smith, J., & Kumpf, M. (1998). Snow leopards (Uncia uncia): family group management alternatives. Anim.Keepers' Forum, 25(10), 386–391.
Abstract: The authors offer insights into creating family groups of snow leopards in zoos. The programs at the Denver Zoo, Denver, Colorado, and at John Ball Zoological Gardens, Grand Rapids, Michigan, are highlighted. lgh.
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Richard, C. (1999). Sectoral Report in Vol II: Developing Strategies for Agriculture and Related Sectors in Ladakh.
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Rieger, I. (1978). Management techniques of captive ounces, (Uncia uncia). Int.Ped.Book of Snow Leopards, 1, 50–70.
Abstract: Presents a comparison of housing and techniques for care and breeding at 16 zoos. Includes comments on factors which may influence breeding
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Rieger, I. (1980). Some difficulty breeding ounces, (Uncia uncia) at zoological gardens. Int.Ped Book of Snow Leopards, 2, 76–95.
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Rieger, I., & Peters, G. (1981). Observations on the mating and vocal behavior of snow leopards (Uncia-uncia) in zoological garden. Zeitschrift Fur Saugetierkunde International Journal of Mamamalian Biology, 46(1), 35–48.
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Roberts, T. J. (1977). The Mammals of Pakistan. London and Tonbridge: Ernest Benn.
Abstract: Brief description of physical characteristics, ecology,status, and distribution of snow leopard in Pakistan
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Rodenburg, W. F. (1977). The Trade in Wild Animal Furs in Afghanistan.
Abstract: Estimated that 70-80 snow leopard pelts were traded annually at the Kabul bazaar.
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Rosenthal, M., & Ott, J. L. (1988). Snow Leopard Captive Mangement Survey. Chicago: Lincon Park Zoological Gardens.
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Roth, T. L., Armstrong, D. L., Barrie, M. T., & Wildt, D. E. (1997). Seasonal effects on ovarian responsiveness to exogenous gonadotrophins and successful artificial insemination in the snow leopard (Uncia uncia). Reprod Fertil Dev, 9(3), 285–295.
Abstract: Ovaries of the seasonally-breeding snow leopard (Uncia uncia) were examined to determine whether they were responsive to exogenous gonadotrophins throughout the year. The potential of laparoscopic artificial insemination (AI) also was assessed for producing offspring. During the non-breeding, pre-breeding, breeding and post-breeding seasons, females (n = 20) were treated with a standardized, dual- hormone regimen given intramuscularly (600 I.U. of equine chorionic gonadotrophin followed 80-84 h later with 300 I.U. of human chorionic gonadotrophin (hCG)). Laparoscopy was performed 45-50 h after administration of hCG, and all ovarian structures were described. Females with fresh corpora lutea (CL) were inseminated, and anovulatory females were subjected to follicular aspiration to examine oocyte quality. Snow leopards responded to exogenous gonadotrophins throughout the year. Mean number of total ovarian structures (distinct follicles mature in appearance plus CL) did not differ (P > or = 0.05) with season, but the proportion of CL: total ovarian structures was greater (P < 0.01) for the breeding season compared with all other seasons. The proportion of females ovulating was greater (P < 0.05) during the breeding and post-breeding seasons than during the pre-breeding and non- breeding seasons respectively. No Grade-1 quality oocytes were recovered from follicles of anovulatory females. Serum concentrations of oestradiol-17 beta appeared elevated in all females, and neither oestradiol-17 beta concentrations nor progesterone concentrations differed (P > or = 0.05) among seasons. Of 15 females artificially inseminated, the only one that was inseminated in the non-breeding season became pregnant and delivered a single cub. This is the first successful pregnancy resulting from AI in this endangered species.
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Roth, T. L., Howard, J. G., Donoghue, A. M., Swanson, W. F., & Wildt, D. E. (1994). Function and culture requirements of snow leopard (Panthera uncia) spermatozoa in vitro. J Reprod Fertil, 101(3), 563–569.
Abstract: Electroejaculates from eight snow leopards were used to determine how the motility of spermatozoa was influenced by (i) type of media (Ham's F10, PBS, human tubal fluid or RPMI-1640); (ii) holding temperature (23 degrees C versus 37 degrees C); (iii) washing of spermatozoa and (iv) a sperm metabolic enhancer, pentoxifylline. The duration of sperm motility was assessed by evaluating samples in each treatment every hour for 6 h and a sperm motility index (a value combining percentage sperm motility and rate of forward progression) calculated. Spermatozoa from the Ham's F10, PBS and PBS plus pentoxifylline treatments were also co-incubated with zona-intact, domestic cat eggs that were fixed and evaluated for spermatozoa bound to the zona pellucida, penetrating the outer and inner layers of the zona pellucida and within the perivitelline space. During the 6 h co-incubation, the sperm motility index in PBS with pentoxifylline was greater (P < 0.05) than in PBS alone which, in turn, was greater (P < 0.05) than in the other three test media. Washing the spermatozoa enhanced (P < 0.05) motility in both PBS and PBS plus pentoxifylline relative to unwashed samples, but there was no effect (P > 0.05) of holding temperature. Pentoxifylline supplementation enhanced (P < 0.05) the proportion of cat eggs with bound, but not penetrated, snow leopard spermatozoa in the inner layer of the zona pellucida, and there were no spermatozoa in the perivitelline space.(ABSTRACT TRUNCATED AT 250 WORDS)
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