|
Oli, M. K. (1997). Winter home range of snow leopards in Nepal. Mammalia, 61(3), 355–360.
Abstract: Because of their low densities, sparse distribution, elusive behavior, and the precipitous habitat they occupy, snow leopards (Uncia uncia) have been the subject of limited study. This study contributes to that limited database with an investigation of the winter home range of 3 radio-collared snow leopards (2 females and 1 male) in the Annapurna Conservation Area, Nepal. Winter home ranges varied from 13.9-22.3 km2 (x = 19.1). Home ranges overlapped extensively within and between sexes, and an area of 8.1 km2 in the core study site was shared by all three leopards.
|
|
|
Khanyari, M., Zhumabai uulu, K., Luecke, S., Mishra, C.,
Suryawanshi, K. (2020). Understanding population baselines: status of mountain ungulate
populations in the Central Tien Shan Mountains, Kyrgyzstan. Mammalia, , 1–8.
Abstract: We assessed the density of argali (Ovis ammon) and ibex
(Capra sibirica) in Sarychat-Ertash Nature Reserve and its neighbouring
Koiluu valley. Sarychat is a protected area, while Koiluu is a human-use
landscape which is a partly licenced hunting concession for mountain
ungulates and has several livestock herders and their permanent
residential structures. Population monitoring of mountain ungulates can
help in setting measurable conservation targets such as appropriate
trophy hunting quotas and to assess habitat suitability for predators
like snow leopards (Panthera uncia). We employed the double-observer
method to survey 573 km2 of mountain ungulate habitat inside Sarychat
and 407 km2 inside Koiluu. The estimated densities of ibex and argali in
Sarychat were 2.26 (95% CI 1.47–3.52) individuals km-2 and 1.54 (95% CI
1.01–2.20) individuals km-2, respectively. Total ungulate density in
Sarychat was 3.80 (95% CI 2.47–5.72) individuals km-2. We did not record
argali in Koiluu, whereas the density of ibex was 0.75 (95% CI
0.50–1.27) individuals km-2. While strictly protected areas can achieve
high densities of mountain ungulates, multi-use areas can harbour
meaningful
though suppressed populations. Conservation of mountain ungulates and
their predators can be enhanced by maintaining Sarychat-like “pristine”
areas interspersed within a matrix of multi-use areas like Koiluu.
|
|
|
Hemmer, H. (1972). Uncia uncia. In Mammalian Species-American Society of Mammalogists (Vol. 20, pp. 1–5).
|
|
|
Fox, J. L., Nurbu, C., & Chundawat, R. S. (1991). Tibetian Argali (Ovis ammon hodgsoni). Mammalia, , 48–51.
|
|
|
Johansson, O., Ausilio, G., Low, M., Lkhagvajav, P., Weckworth,
B., Sharma, K. (2020). The timing of breeding and independence for snow leopard females
and their cubs. Mammalian Biology, .
Abstract: Significant knowledge gaps persist on snow leopard demography
and reproductive behavior. From a GPS-collared population in Mongolia,
we estimated the timing of mating, parturition and independence. Based
on three mother–cub pairs, we describe the separation phase of the cub
from its mother as it gains independence. Snow leopards mated from
January–March and gave birth from April–June. Cubs remained with their
mother until their second winter (20–22 months of age) when cubs started
showing movements away from their mother for days at a time. This
initiation of independence appeared to coincide with their mother mating
with the territorial male. Two female cubs remained in their mothers’
territory for several months after initial separation, whereas the male
cub quickly dispersed. By comparing the relationship between body size
and age of independence across 11 solitary, medium-to-large felid
species, it was clear that snow leopards have a delayed timing of
separation compared to other species. We suggest this may be related to
their mating behavior and the difficulty of the habitat and prey capture
for juvenile snow leopards. Our results, while limited, provide
empirical estimates for understanding snow leopard ecology and for
parameterizing population models.
|
|
|
Valdez, R., Michel, S., Subbotin, A., Klich, D. (). Status and population structure of a hunted population of Marco Polo Argali Ovis ammon polii (Cetartiodactyla, Bovidae) in Southeastern Tajikistan. Mammalia, 80(1), 49–57.
Abstract: Marco Polo sheep (Ovis ammon polii), listed as Near Threatened in the IUCN Red List, were surveyed using vehicles during three summers and three consecutive winters to determine the status and population structure of the subspecies in a hunted population in southeastern Pamirs, Tajikistan. A total of 8649, 8392, and 7663 sheep were observed in each winter survey with densities of 5.42,
4.91, and 4.49 argalis/km2, respectively. The differences in numbers observed in different years were probably due principally to differing dates of surveys among years. The high ratios of lamb for every 100 ewe (53, 38, and 49 during the winter surveys, and 60, 45, and 58 during the summer
surveys) and high percentages (45%–50%) of mature females during winter indicate that offspring recruitment is sufficient to maintain a stable population. The significant
increase in the abundance of Marco Polo sheep in the Tajikistan Pamirs compared with that of previous population surveys may probably be attributed to low numbers of domestic livestock during the winter, low human population density, unfenced and widespread wild sheep habitats,
and rigorous patrolling to limit poaching. The small number (45) of hunting permits has a minimal impact on the male sheep sector. Tajikistan now supports more argali than any other country
|
|
|
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.
|
|
|
Johnson, W. E., Dratch, P. A., Martenson, J. S., & O'Brien, S. J. (1996). Resolution of recent radiations within three evolutionary lineages of Felidae using mitochondrial restriction fragment length polymorphism variation. Journal of Mammalian Evolution, 3(2), 97–120.
Abstract: Patterns of mitochondrial restriction fragment length polymorphism (RFLP) variation were used to resolve more recent relationships among the species of the Felidae ocelot lineage, domestic cat lineage, and pantherine lineage. Twenty-five of 28 restriction enzymes revealed site variation in at least 1 of 21 cat species. The ocelot lineage was resolved into three separate sister taxa groups: Geoffroy's cat (Oncifelis geoffroyi) and kodkod (O. guigna), ocelot (Leopardus pardalis) and margay (L. wiedii), and pampas cat (Lynchailurus colocolo) and most of the tigrina samples (Leopardus tigrina). Within the domestic cat lineage, domestic cat (Felis catus), European wild cat (F. silvestris), and African wild cat (F. libyca) formed a monophyletic trichotomy, which was joined with sand cat (F. margarita) to a common ancestor. Jungle cat (F. chaus) and black-footed cat (F. nigripes) mtDNAs diverged earlier than those of the other domestic cat lineage species and are less closely related. Within the pantherine lineage, phylogenetic analysis identified two distinct groups, uniting lion (P. leo) with leopard (P. pardus) and tiger (P. tigris) with snow leopard (P. uncia).
|
|
|
Schaller, G. B., & Mirza, Z. B. (1971). On the behaviour of Kashmir Markhor (Capra falconeri cashmiriensis). Mammalia, 35, 548–566.
Abstract: Notes snow leopard as main predator in Pakistan study area. Describes content of some snow leopard droppings
|
|
|
Fox, J. L., & Chundawat, R. S. (1988). Observations of snow leopard stalking, killing and feeding behavior. Mammalia, 52(1), 137–140.
|
|