|
|
Machado, C., Brown, P., & Turner, R. (1984). Dental crown restorations on a snow leopard. Journal Of Zoo Animal Medicine, 15(4), 146–150.
Abstract: In the spring of 1983 the San Francisco Zoo received a female snow leopard (Panthera uncia) as part of an exotic animal exchange program with the People's Republic of China. Upon examination, it was found that this nine-yea old, seventy-five pound, wild-trapped animal had sustained considerable dental injuries, including fractures of all maxillary and mandibular anterior teeth. The purpose of this paper is to describe the dental procedures undertaken to restore the physiological function of all four canines.
|
|
|
|
Oli, M. K., Taylor, I. R., & Rogers, M. K. (1993). Diet of the snow leopard (Panthera uncia) in the Annapurna Conservation Area, Nepal. Journal of Zoology London, 231(3), 365–370.
Abstract: The diet of the snow leopard (Panthera uncia) was studied from 213 scats collected between April 1990 and February 1991 in the Annapurna Conservation Area, Nepal. Seven species of wild and five species of domestic mammals were taken, as well as an unidentified mammal and birds. Blue sheep (Pseudois nayaur) were the most frequently eaten prey. Himalayan marmots (Marmota himalayana) were also important, except in winter when they were hibernating. During winter, snow leopards ate more Royle's pika (Ochotona roylei) and domestic livestock. Yaks were eaten more frequently than other livestock types.
|
|
|
|
Oli, M. K. (1993). A key for the identification of the hair of mammals of a snow leopard (Panthera uncia) habitat in Nepal. Journal of Zoology London, 231(1), 71–93.
Abstract: Analysis of prey remains in scats, particularly hairs, in widely used to study diet of mammalian predators, but identification of hair is often difficult because hair structures vary considerably both within and between species. Use of photographic reference of diagnostically important hair structures from mammals occurring in a predator's habitat has been found to be convenient for routine identification. A photographic reference key was developed for the identification of hairs of the mammals known to occur in a snow leopard (Panthera uncia) habitat in the Annapurna Conservation Area, Nepal. The key included a photographic reference of the diagnostic hair structures of nine species of wild and five species of domestic mammals. The cross-sectional appearance, shape and arrangement of medulla, the ratio of cortex to medulla, and the form and distribution of pigment in medulla and cortex were important diagnostic aids in the identification of hairs.
|
|
|
|
Kazensky, C. A., Munson, L., & Seal, U. S. (1998). The effects of melengestrol acetate on the ovaries of captive wild felids. Journal-of-Zoo-and-Wildlife-Medicine, 29(1), 1–5.
Abstract: Melengestrol acetate (MGA) is the most widely used contraceptive in zoo felids, but the mechanism of contraception and the pathologic effects have not been investigated. For this study, the effects of MGA on folliculogenesis were assessed, and the association of MGA with ovarian lesions was evaluated. Comparisons were made among the histopathologic findings in the ovaries from 88 captive wild felids (representing 15 species) divided into three groups: 37 currently contracepted with MGA, eight previously exposed to MGA, and 43 never contracepted. Ninety-one percent of the felids evaluated had tertiary follicles, and no differences were noted between contracepted and uncontracepted cats. Some MGA-contracepted cats also had corpora lutea indicating recent ovulation. These results indicate that folliculogenesis is not suppressed by current doses of MGA and ovulation occurred in some cats. Therefore, the contraceptive actions of MGA do not occur by suppressing folliculogenesis, and MGA-contracepted felids likely have endogenous estrogens that may confound progestin effects on the uterus. Cystic rete ovarii was the most common pathologic finding, but they were not more prevalent in MGA-contracepted cats. These findings indicate that MGA is not associated with ovarian disease, including ovarian cancer, in contrast to the uterine lesions noted in MGA-treated cats.
|
|
|
|
Kinsel, M. J., Kovarik, P., & Murnane, R. D. (1998). Gastric spiral bacteria in small felids. Journal-of-Zoo-and-Wildlife-Medicine, 29(2), 214–220.
Abstract: Nine small cats, including one bobcat (Felis rufus), one Pallas cat (F. manul), one Canada lynx (F. lynx canadensis), two fishing cats (F. viverrina), two margays (F. wiedii), and two sand cats (F. margarita), necropsied between June 1995 and March 1997 had large numbers of gastric spiral bacteria, whereas five large cats, including one African lion (Panthera leo), two snow leopards (P. uncia), one Siberian tiger (P. tigris altaica), and one jaguar (P. onca), necropsied during the same period had none. All of the spiral organisms from the nine small cats were histologically and ultrastructurally similar. Histologically, the spiral bacteria were 5-14 mum long with five to nine coils per organism and were located both extracellularly within gastric glands and surface mucus, and intracellularly in parietal cells. Spiral bacteria in gastric mucosal scrapings from the Canada lynx, one fishing cat, and the two sand cats were gram negative and had corkscrew-like to tumbling motility when viewed with phase contrast microscopy. The bacteria were 0.5-0.7 mum wide, with a periodicity of 0.65-1.1 mum in all cats. Bipolar sheathed flagella were occasionally observed, and no periplasmic fibrils were seen. The bacteria were extracellular in parietal cell canaliculi and intracellular within parietal cells. Culture of mucosal scrapings from the Canada lynx and sand cats was unsuccessful. Based on morphology, motility, and cellular tropism, the bacteria were probably Helicobacter-like organisms. Although the two margays had moderate lymphoplasmacytic gastritis, the other cats lacked or had only mild gastric lymphoid infiltrates, suggesting that these organisms are either commensals or opportunistic pathogens.
|
|
|
|
Pohl, J. (1996). Tracking the Big Cat. Juneau Empire (AK), 5.
Abstract: Juneau biologist Tom McCarthy will make one last trip to Mongolla to finish researching snow leopards – which are poached for their pelts and killed for the medicinal value of their bones – so he can recommend ways to preserve the elusive animals and their habitat
|
|
|
|
Chakraborty, R. E., & Chakraborty, S. (1996). Identification of dorsal guard hairs of Indian species of the genus Panthera Oken (Carnivora: Felidae). Mammalia, 60(3), 480.
Abstract: Dorsal guard hairs of four living Indian species of the genus Panthera, viz. P. tigris, P. leo, P. pardus and P. uncia have been studied. It is found that the characters are somewhat overlapping, but identification of the species may be possible from the combination of characters.
|
|
|
|
Fox, J. L., & Chundawat, R. S. (1988). Observations of snow leopard stalking, killing and feeding behavior. Mammalia, 52(1), 137–140.
|
|
|
|
Fox, J. L., Nurbu, C., & Chundawat, R. S. (1991). Tibetian Argali (Ovis ammon hodgsoni). Mammalia, , 48–51.
|
|
|
|
Oli, M. K. (1996). Seasonal patterns in habitat use of blue sheep Pseudois nayaur (Artiodactyla, Bovidae) in Nepal. Mammalia, 60(2), 187–193.
Abstract: Blue sheep (Pseudois nayaur) are the main prey of the endangered snow leopard (Panthera uncia) as well as an important game species in Nepal. A knowledge of how blue sheep utilize their habitat is essential for the scientific management of the sheep and for the conservation of the snow leopard, but we only have a limited understanding of this aspect of blue sheep ecology. I studied the habitat use pattern of blue sheep by direct observation in the Anna-purna Conservation Area, Nepal where they occur sympatrically with the snow leopard. The sheep used grassland habitats more frequently during pre-parturition (spring) and post-parturition (autumn) than other habitat types, but scrub and grassland habitats were used equally frequently during the rut (winter). The sheep used smooth undulating slopes of medium steepness (<40 degrees) on southerly aspects within the elevation range of 4,200-4,600 m most frequently in all seasons, and there was no evidence of seasonal migration along the elevation gradient. When not in broken landforms (e.g., cliff, landslides), the sheep maintained proximity (less than or equal to 150 m) to such features suggesting their importance as escape cover (i.e., from predators). The use of habitat components by blue sheep appeared to be related to the distribution of foraging areas and escape cover.
|
|
