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Wang, X., & Schaller, G. B. (1996). Status of large mammals in Western Inner Mongolia, China. Journal of East China Normal University (Special Issue of Zoology), , 93–104.
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Wang, X., Peng, J., & Zhou, H. (2000). Preliminary observations on the distribution and status of dwarf blue sheep Pseudois schaeferi. Oryx, 34(1), 21–26.
Abstract: Describes the drastic decline of the dwarf blue sheep since the 1950's primarily due to over-hunting. There are an estimated 200 individuals remaining in a 295 square km range in Batang county, China. The authors recommend urgent protection for this species.
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Wangchuk, R., & Jackson, R. (2009). A Community-based Approach to Mitigating Livestock-Wildlife Conflict in Ladakh, India.
Abstract: Livestock depredation by snow leopard and wolf is widespread across the Himalayan region (Jackson et al. 1996, Jackson and Wangchuk 2001; Mishra 1997, Oli et al 1994). For example, in India's Kibber Wildlife Sanctuary, Mishra (1997) reported losses amounting to 18% of the livestock holdings and valued at about US $138 per household. The villagers claimed predation rates increased after establishment of the sanctuary, but
surveys indicated a dramatic increase in livestock numbers accompanying changes in animal husbandry systems (Mishra 2000).
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Wangchuk, T. R. (1992). Snow Leopard: Its Management with Emphasis on Bhutan.
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Ward, A. E. (1921). Game animals of Kashmir and adjacent hill provinces. J.of Bombay Natural Historical Society., 29, 23–35.
Abstract: comments that snow leopard may take blue sheep as prey
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Warren E.Johnson, E. E. (2006). The Late Miocene Radiation of Modern Felidae: A Genetic Assessment (Stephen J.O'Brien Emma Teeling Agostinho Antunes W. J. M. Jill Pecon-Slattery, Ed.) (Vol. 311). Washington D.C.
Abstract: Modern felid species descend from relatively recent (<11 million years ago) divergence and
speciation events that produced successful predatory carnivores worldwide but that have
confounded taxonomic classifications. A highly resolved molecular phylogeny with divergence dates
for all living cat species, derived from autosomal, X-linked, Y-linked, and mitochondrial gene
segments (22,789 base pairs) and 16 fossil calibrations define eight principal lineages produced
through at least 10 intercontinental migrations facilitated by sea-level fluctuations. A ghost lineage
analysis indicates that available felid fossils underestimate (i.e., unrepresented basal branch
length) first occurrence by an average of 76%, revealing a low representation of felid lineages
in paleontological remains. The phylogenetic performance of distinct gene classes showed that
Y-chromosome segments are appreciably more informative than mitochondrial DNA, X-linked,
or autosomal genes in resolving the rapid Felidae species radiation.
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Wasser, S. (1998). Snow Leopard Genetics: New Techniques (Vol. xvi). Seattle: Islt.
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Watanabe, M., Sugano, S., Togashi, T., Imai, J., Uchida, K., Yamaguchi, R., et al. (2000). Molecular cloning and phylogenetic analysis of canine beta-casein. DNA Seq, 11(3-4), 295–300.
Abstract: A canine beta-casein cDNA was isolated from mammary tissue by polymerase chain reaction (PCR) using degenerate primers. It encodes 250 amino acids protein containing the conserved sequence motif of beta- casein. It showed the highest homology with snow-leopard (Uncia uncia (55-62% identity). It also showed 44-53% identity with human, 33-42%, identity with mouse, 29-37%, identity with rat, 43-53% identity with rabbit, 41-48% identity with pig, 44-51% identity with cattle and 44- 50% identity with sheep. A 1.2-kb mRNA was detected in mammary tissue by Northern blot analysis. Phylogenetic analysis revealed that canine beta-casein formed a branch with lesser panda and snow leopard, which were grouped into carnivore.
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Wei, L., Wu, X., & Jiang, Z. (2008). The complete mitochondrial genome structure of snow leopard Panthera uncia.
Abstract: The complete mitochondrial genome (mtDNA) of snow leopard Panthera uncia was obtained by using the polymerase chain reaction (PCR) technique based on the PCR fragments of 30 primers we designed. The entire mtDNA sequence was 16 773 base pairs (bp) in length, and the base composition was: A-5,357ª“,Ž+bp (31.9%); C-4,444ª”,Ž+bp (26.5%); G-2,428ª“,Ž+bp (14.5%); T-4,544ª”,Ž+bp (27.1%). The structural characteristics [0] of the P. uncia mitochondrial genome were highly similar to these of Felis catus, Acinonyx jubatus, Neofelis nebulosa and other mammals. However, we found several distinctive features of the mitochondrial genome of Panthera unica. First, the termination codon of COIII was TAA, which differed from those of F. catus, A. jubatus and N. nebulosa. Second, tRNASer (AGY), which lacked the ''DHU'' arm, could not be folded into the typical cloverleaf-shaped structure. Third, in the control region, a long repetitive sequence in RS-2 (32ª“,Ž+bp) region was found with 2 repeats while one short repetitive segment (9ª”,Ž+bp) was found with 15 repeats in the RS-3 region. We performed phylogenetic analysis based on a 3 816ª",Ž+bp concatenated sequence of 12S rRNA, 16S rRNA, ND2, ND4, ND5, Cyt b and ATP8 for P. uncia and other related species, the result indicated that P. uncia and P. leo were the sister species, which was different from the previous findings. (c) 2008 Springer Science+Business Media B.V.
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Weilemann P. (1982). Experiences in births of snow leopards in Zurich Zoo. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 3 (Vol. 3, pp. 111–116). Helsinki: Helsinki Zoo.
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