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Saltz, D., Rowen, M., & Rubenstein, D. (2000). The effect of space-use patterns of reintroduced Asiatic wild ass on effective population size. Conservation Biology, 14(6), 1852–1861.
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Korablev, M. P., Poyarkov, A. D., Karnaukhov, A. S., Zvychaynaya, E. Y., Kuksin, A. N., Malykh, S. V., Istomov, S. V., Spitsyn, S. V., Aleksandrov, D. Y., Hernandez-Blanco, J. A., Munkhtsog, B., Munkhtogtokh, O., Putintsev, N. I., Vereshchagin, A. S., Becmurody, A., Afzunov, S., Rozhnov, V. V. (2021). Large-scale and fine-grain population structure and genetic diversity of snow leopards (Panthera uncia Schreber, 1776) from the northern and western parts of the range with an emphasis on the Russian population. Conservation Genetics, .
Abstract: The snow leopard (Panthera uncia Schreber, 1776) population in Russia and Mongolia is situated at the northern edge of the range, where instability of ecological conditions and of prey availability may serve as prerequisites for demographic instability and, consequently, for reducing the genetic diversity. Moreover, this northern area of the species distribution is connected with the western and central parts by only a few small fragments of potential habitats in the Tian-Shan spurs in China and Kazakhstan. Given this structure of the range, the restriction of gene flow between the northern and other regions of snow leopard distribution can be expected. Under these conditions, data on population genetics would be extremely important for assessment of genetic diversity, population structure and gene flow both at regional and large-scale level. To investigate large-scale and fine-grain population structure and levels of genetic diversity we analyzed 108 snow leopards identified from noninvasively collected scat samples from Russia and Mongolia (the northern part of the range) as well as from Kyrgyzstan and Tajikistan (the western part of the range) using panel of eight polymorphic microsatellites. We found low to moderate levels of genetic diversity in the studied populations. Among local habitats, the highest heterozygosity and allelic richness were recorded in Kyrgyzstan (He = 0.66 ± 0.03, Ho = 0.70 ± 0.04, Ar = 3.17) whereas the lowest diversity was found in a periphery subpopulation in Buryatia Republic of Russia (He = 0.41 ± 0.12, Ho = 0.29 ± 0.05, Ar = 2.33). In general, snow leopards from the western range exhibit greater genetic diversity (He = 0.68 ± 0.04, Ho = 0.66 ± 0.03, Ar = 4.95) compared to those from the northern range (He = 0.60 ± 0.06, Ho = 0.49 ± 0.02, Ar = 4.45). In addition, we have identified signs of fragmentation in the northern habitat, which have led to significant genetic divergence between subpopulations in Russia. Multiple analyses of genetic structure support considerable genetic differentiation between the northern and western range parts, which may testify to subspecies subdivision of snow leopards from these regions. The observed patterns of genetic structure are evidence for delineation of several management units within the studied populations, requiring individual approaches for conservation initiatives, particularly related to translocation events. The causes for the revealed patterns of genetic structure and levels of genetic diversity are discussed.
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Robinson, J. J., Crichlow, A. D., Hacker, C. E., Munkhtsog, B., Munkhtsog, B., Zhang, Y., Swanson, W. F., Lyons, L. A., Janecka, J. E. (2024). Genetic Variation in the Pallas’s Cat (Otocolobus manul) in Zoo-Managed and Wild Populations. Diversity, 16(228), 1–13.
Abstract: The Pallas’s cat (Otocolobus manul) is one of the most understudied taxa in the Felidae family. The species is currently assessed as being of “Least Concern” in the IUCN Red List, but this assessment is based on incomplete data. Additional ecological and genetic information is necessary for the long-term in situ and ex situ conservation of this species. We identified 29 microsatellite loci with sufficient diversity to enable studies into the individual identification, population structure, and phylogeography of Pallas’s cats. These microsatellites were genotyped on six wild Pallas’s cats from the Tibet Autonomous Region and Mongolia and ten cats from a United States zoo-managed population that originated in Russia and Mongolia. Additionally, we examined diversity in a 91 bp segment of the mitochondrial 12S ribosomal RNA (MT-RNR1) locus and a hypoxia-related gene, endothelial PAS domain protein 1 (EPAS1). Based on the microsatellite and MT-RNR1 loci, we established that the Pallas’s cat displays moderate genetic diversity. Intriguingly, we found that the Pallas’s cats had one unique nonsynonymous substitution in EPAS1 not present in snow leopards (Panthera uncia) or domestic cats (Felis catus). The analysis of the zoo-managed population indicated reduced genetic diversity compared to wild individuals. The genetic information from this study is a valuable resource for future research into and the conservation of the Pallas’s cat.
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Subbotin, A. E., & Istomov, S. V. (2009). The population status of snow leopards Uncia uncia (Felidae, Carnivora) in the western Sayan Mountain Ridge. Doklady Biologicl Sciences, 425, 183–186.
Abstract: The snow leopard (Uncia uncial Schreber, 1776) is the most poorly studied species of the cat family in the world and, in particular, in Russia, where the northern periphery of the species area (no more than 3% of it) is located in the Altai-Hangai-Sayan range [1]. It is generally known that the existing data on the Russian part of the snow leopard population have never been a result of targeted studies; at best, they have been based on recording the traces of the snow leopard vital activity [2]. This is explained by the snow leopard's elusive behavior, inaccessibility of its habitats for humans, and its naturally small total numbers in the entire species area. All published data on the population status of the snow leopard in Russia, from the first descriptions of the species [3-6] to the latest studies [7, 8] are subjective, often speculative, and are not confirmed by
quantitative estimates. It is obvious, however, that every accurate observation of this animal is of particular interest [9]. The purpose of our study was to determine the structure and size of the population group presumably inhabiting the Western Sayan mountain ridge at the northern boundary of the species area
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Ferretti, F., Lovari, S., Minder, I., Pellizzi, B. (2014). Recovery of the snow leopard in Sagarmatha (Mt.Everest) National Park: effects on main prey. European Journal of Wildlife Research, (60), 559–562.
Abstract: Consequences of predation may be particularly
heavy on small populations of herbivores, especially if they
are threatened with extinction. Over the 2006–2010 period, we
documented the effects of the spontaneous return of the endangered
snow leopard on the population of the vulnerable
Himalayan tahr. The study area was an area of central
Himalaya where this cat disappeared c. 40 years before, because
of persecution by man. Snow leopards occurred mainly
in areas close to the core area of tahr distribution. Tahr was the
staple (56.3 %) of snow leopards. After the arrival of this cat,
tahr decreased by more than 2/3 from 2003 to 2010 (mainly
through predation on kids). Subsequently, the density of snow
leopards decreased by 60%from2007 to 2010. The main prey
of snow leopards in Asia (bharal, marmots) were absent in our
study area, forcing snow leopards to specialize on tahr. The
restoration of a complete prey spectrum should be favoured
through reintroductions, to conserve large carnivores and to
reduce exploitation of small populations of herbivores, especially
if threatened.
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Ahmad, S., Ali, H., Asif, M., Khan, T, Din, N., Rehman, E. U., Hameed, S., Din, J. U., Nawaz, M. A. (2022). Spatial density pattern of Himalayan Ibex (Capra sibirica) in Pakistan. Global Ecology & Conservation, 39(e02288), 1–12.
Abstract: Mountain ungulates perform a key role in maintaining the balance of ecosystems as they are the primary consumers of vegetation and prey for large predators. The mountain ranges of northern Pakistan are home to six species of mountain ungulates, and the Himalayan ibex (Capra sibirica), hereafter ibex, is the most abundant among them. This study was conducted in three administrative regions of northern Pakistan, viz. Gilgit-Baltistan (GB), Azad Jammu and Kashmir (AJK), and Khyber Pakhtunkhwa (KP), to generate a range-wide density pattern map of ibex. A double-observer survey was conducted in 25 study sites during 2018–2021 across the ibex distribution range, covering an area of about 35,307 km2, by walking transects totaling 1647 km. Within the ibex range where the survey was not conducted due to financial and logistical constraints, we obtained species population information from local wildlife departments’ most recent annual survey data. The aim was to generate a density map for the entire ibex range. Using the BBRe-capture package in program R, we estimated an ibex population of 7639 (95 % CI) with a mean density of 0.21/km2 in the surveyed area. Combining with the secondary data from un-surveyed areas, the total population estimate for the country came to 10,242 ibex. The largest population densities were observed in four valleys (Shimshal, Gulkin-Hussaini, Khyber, and Khunjerab) of the Karakoram-Pamir range, followed by the Hindu Kush range (Chitral Wildlife Division [WD]). The central and eastern parts of the Karakoram range had moderate to low densities, while the Himalayan range (e.g., Astore Valley) supported a small population. The mean herd size was 15 individuals (range: 5–41), and the average detection probability of observers A and B was 0.69 and 0.48, respectively. The average male and young ratios per 100 females were estimated to be 75 and 81, respectively. The range-wide density map developed during the study provided an evidence for the impact of trophy hunting programs and an objective tool for range-wide conservation planning of the species.
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Zhirjakov, V. A. (1990). On the ecology of the snow leopard in the Zailisky-Alatau (Northern Tien Shan). Int Ped Book of Snow Leopards, 6, 25–30.
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Smirnov, M. N., Sokolov, G. A., & Zyryanov, A. N. (1990). The Snow Leopard (Uncia Uncia Scherber 1776) in Siberia. Int.Nat.Ped.Book of Snow Leopards, 6, 9–15.
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Koshkarev, E. P. (1990). On the environment-related stability of snow leopard (Uncia uncia) populations in connection with their distribution in the natural habitats and changes for spread within the USSR. Int.Ped.Book of Snow Leopards, 6, 37–50.
Abstract: The stability of animal populations in respect of the influence of the environment is well known to be conditioned by their location in the natural habitat and their ability to establish new territories. In the peripheral regions of natural habitat, however-in the zone that is ecologically least favourable-the situation of the animal is most unstable. This is due to increased pressure of environmental factors which favour neither a high frequency of contacts between individuals belonging to sperate populations nor an increase in the number of such contatcs and their stabilization. In our opinion, this describes the situation that has come about in certain regions inhabited by the snow leopard in the Soviet Union.
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Sokov, A. I. (1990). The present status of the snow leopard population in the south western Pamir-Altai Mountains (Tadzhikistan). Int.Ped.Book of Snow Leopards, 6, 33–36.
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Jackson, R., & Ahlborn, G. (1990). The role of protected areas in Nepal in maintaining viable populations of snow leopards. Int.Ped.Book of Snow Leopards, 6, 51–69.
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Blomqvist, L. (1995). Three decades of Snow Leopards Panthera uncia in Captivity. Int.Zoo Yearbook, 34, 178–185.
Abstract: The author reports the status of the captive population of snow leopards over the last three decades. Genetic and demographic information is also provided. The captive population as of 1992 was 541 leopards. klf. I
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Poyarkov, A. D., Munkhtsog, B., Korablev, M. P., Kuksin, A. N., Alexandrov, D. Y., Chistopolova, M. D., Hernandez-Blanco, J. A., Munkhtogtokh, O., Karnaukhov, A. S., Lkhamsuren, N., Bayaraa, M., Jackson, R. M., Maheshwari, A., Rozhnov, V. V. (2020). Assurance of the existence of a trans-boundary population of the snow leopard (Panthera uncia) at Tsagaanshuvuut – Tsagan- Shibetu SPA at the Mongolia-Russia border. Integrative Zoology, (15), 224–231.
Abstract: The existence of a trans-boundary population of the snow leopard (Panthera uncia) that inhabits the massifs of Tsagaanshuvuut (Mongolia) – Tsagan-Shibetu (Russia) was determined through non-invasive genetic analysis of scat samples and by studying the structure of territory use by a collared female individual. The genetic analysis included species identification of samples through sequencing of a fragment of the cytochrome b gene and individual identification using a panel of 8 microsatellites. The home range of a female snow leopard marked with a satellite Global Positioning System (GPS) collar was represented by the minimum convex polygon method (MCP) 100, the MCP 95 method and the fixed kernel 95 method. The results revealed insignificant genetic differentiation between snow leopards that inhabit both massifs (minimal fixation index [FST]), and the data testify to the unity of the cross-border group. Moreover, 5 common individuals were identified from Mongolian and Russian territories. This finding clearly shows that their home range includes territories of both countries. In addition, regular movement of a collared snow leopard in Mongolia and Russia confirmed the existence of a cross-border snow leopard group. These data support that trans-boundary conservation is important for snow leopards in both countries. We conclude that it is crucial for Russia to study the northern range of snow leopards in Asia.
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Blomqvist, L. (2003). The global snow leopard population in captivity 2001 (Vol. 8).
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Blomqvist, L. (1980). The 1979 world register for the captive population of snow leopards, Panthera uncia. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards (pp. 62–75). Helsinki: Helsinki Zoo.
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Blomqvist, L. (1982). The 1981 annual report of the captive snow leopards (Panthera uncia) population. International Pedigree Book of Snow Leopards, 3.
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Freeman, H. (1980). The snow leopard, today and yesterday. In L. Blomqvist (Ed.), International Pedigree Book of Snow Leopards, Vol. 2 (Vol. 2, pp. 37–43). Helsinki: Helsinki Zoo.
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Blomqvist, L. (1979). The 1978 register for the captive population of snow leopards, Panthera uncia. International Zoo News, 26(7-8), 17–23.
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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.
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Durbach, I., Borchers, D., Sutherland, C., Sharma, K. (2020). Fast, flexible alternatives to regular grid designs for spatial
capture–recapture..
Abstract: Spatial capture–recapture (SCR) methods use the location of
detectors (camera traps, hair snares and live-capture traps) and the
locations at which animals were detected (their spatial capture
histories) to estimate animal density. Despite the often large expense
and effort involved in placing detectors in a landscape, there has been
relatively little work on how detectors should be located. A natural
criterion is to place traps so as to maximize the precision of density
estimators, but the lack of a closed-form expression for precision has
made optimizing this criterion computationally demanding. 2. Recent
results by Efford and Boulanger (2019) show that precision can be well
approximated by a function of the expected number of detected
individuals and expected number of recapture events, both of which can
be evaluated at low computational cost. We use these results to develop
a method for obtaining survey designs that optimize this approximate
precision for SCR studies using count or binary proximity detectors, or
multi-catch traps. 3. We show how the basic design protocol can be
extended to incorporate spatially varying distributions of activity
centres and animal detectability. We illustrate our approach by
simulating from a camera trap study of snow leopards in Mongolia and
comparing estimates from our designs to those generated by regular or
optimized grid designs. Optimizing detector placement increased the
number of detected individuals and recaptures, but this did not always
lead to more precise density estimators due to less precise estimation
of the effective sampling area. In most cases, the precision of density
estimators was comparable to that obtained with grid designs, with
improvement in some scenarios where approximate CV(¬D) < 20% and density
varied spatially. 4. Designs generated using our approach are
transparent and statistically grounded. They can be produced for survey
regions of any shape, adapt to known information about animal density
and detectability, and are potentially easier and less costly to
implement. We recommend their use as good, flexible candidate designs
for SCR surveys when reasonable knowledge of model parameters exists. We
provide software for researchers to construct their own designs, in the
form of updates to design functions in the r package oSCR.
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Suryawanshi, K. R., Bhatnagar, Y., & Mishra, C. (2009). Why should a grazer browse? Livestock impact on winter resource use by bharal Pseudois nayaur
. Oecologia, , 1–10.
Abstract: Many mammalian herbivores show a temporal diet variation between graminoid-dominated and browse dominated diets. We determined the causes of such a diet shift and its implications for conservation of a medium sized ungulate-the bharal Pseudois nayaur. Past studies show that the bharal diet is dominated by graminoids (>80%) during summer, but the contribution of graminoids declines to about 50% in winter. We tested the predictions generated by two alternative hypotheses explaining the decline: low graminoid availability during winter causes bharal to include browse in their diet; bharal include browse, with relatively higher nutritional quality, in their diet to compensate for the poor quality of graminoids during winter. We measured winter graminoid availability in areas with no livestock grazing, areas with relatively moderate livestock grazing, and those with intense livestock grazing pressures. The chemical composition of plants contributing to the bharal diet was analysed. The bharal diet was quantiWed through signs of feeding on vegetation at feeding locations. Population structures of bharal populations were recorded using a total count method. Graminoid availability was highest in areas without livestock grazing, followed by areas with moderate and intense livestock grazing. The bharal diet was dominated by graminoids (73%) in areas with highest graminoid availability. Graminoid contribution to the bharal diet declined monotonically (50, 36%) with a decline in graminoid availability. Bharal young to female ratio was 3 times higher in areas with high graminoid availability than areas with low graminoid availability. The composition of the bharal winter diet was governed predominantly by the availability of graminoids in the rangelands. Our results suggest that bharal include more browse in their diet during winter due to competition from livestock for graminoids. Since livestock grazing reduces graminoid availability, creation of livestock-free areas is necessary for the conservation of grazing species such as the bharal and its predators including the endangered snow leopard in the Trans-Himalaya.
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Reading, R. P., Amgalanbaatar, S., Mix, H., & Lhagvasuren, B. (1997). Argali Ovis ammon surveys in Mongolia's South Gobi. Oryx, 31(4), 285–294.
Abstract: Claims poaching and competition with domestic livestock are threatening the argali's survival in Mongolia. The author's conducted aerial and ground surveys in the South Gobi and estimated a populaton size of approximately 3,900 argali.
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Mallon, D. P., Jackson, R. M. (2017). A downlist is not a demotion: Red List status and reality. Oryx, , 1–5.
Abstract: Assessments of biodiversity status are needed to
track trends, and the IUCN Red List has become the accepted
global standard for documenting the extinction
risk of species. Obtaining robust data on population size is
an essential component of any assessment of a species� status,
including assessments for the IUCN Red List. Obtaining
such estimates is complicated by methodological and
logistical issues, which are more pronounced in the case of
cryptic species, such as the snow leopard Panthera uncia.
Estimates of the total population size of this species have,
to date, been based on little more than guesstimates, but a
comprehensive summary of recent field research indicates
that the conservation status of the snow leopard may be
less dire than previously thought. A revised categorization,
from Endangered to Vulnerable, on the IUCN Red List was
proposed but met some opposition, as did a recent, similar
recategorization of the giant panda Ailuropoda melanoleuca.
Possible factors motivating such attitudes are discussed.
Downlisting on the IUCN Red List indicates that the species
concerned is further from extinction, and is always to be
welcomed, whether resulting from successful conservation
intervention or improved knowledge of status and trends.
Celebrating success is important to reinforce the message
that conservation works, and to incentivize donors.
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Aruge, S., Batool, H., Khan, F. M., Abbas, F. I., Janjua, S. (2019). A pilot study�genetic diversity and population structure of snow leopards of Gilgit-Baltistan, Pakistan, using molecular techniques. PeerJ, (7672), 1–14.
Abstract: Background: The Hindu Kush and Karakoram mountain ranges in Pakistan�s northern areas are a natural habitat of the snow leopard (Panthera uncia syn. Uncia uncia) but the ecological studies on this animal are scarce since it is human shy by nature and lives in dif!cult mountainous tracts. The pilot study is conducted to exploit the genetic diversity and population structure of the snow leopard in this selected natural habitat of the member of the wildcat family in Pakistan.
Method: About 50 putative scat samples of snow leopard from !ve localities of Gilgit-Baltistan (Pakistan) along with a control sample of zoo maintained male snow leopard were collected for comparison. Signi!cant quality and quantity of genomic DNA was extracted from scat samples using combined Zhang�phenol�chloroform method and successful ampli!cation of cytochrome c oxidase I gene (190 bp) using mini-barcode primers, seven simple sequence repeats (SSR) markers and Y-linked AMELY gene (200 bp) was done.
Results: Cytochrome c oxidase I gene sequencing suggested that 33/50 (66%) scat samples were of snow leopard. AMELY primer suggested that out of 33 ampli!ed samples, 21 (63.63%) scats were from male and 12 (36.36%) from female leopards. Through successful ampli!cation of DNA of 25 out of 33 (75.75%) scat samples using SSR markers, a total of 68 alleles on seven SSR loci were identi!ed, showing low heterozygosity, while high gene "ow between population.
Discussion: The low gene flow rate among the population results in low genetic diversity causing decreased diversi!cation. This affects the adaptability to climatic changes, thus ultimately resulting in decreased population size of the species.
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Suryawanshi, K. R., Khanyari, M., Sharma, K., Lkhagvajav, P., Mishra, C. (2019). Sampling bias in snow leopard population estimation studies. Population Eccology, , 1–9.
Abstract: Accurate assessments of the status of threatened species and their conservation
planning require reliable estimation of their global populations and robust monitoring
of local population trends. We assessed the adequacy and suitability of studies
in reliably estimating the global snow leopard (Panthera uncia) population. We
compiled a dataset of all the peer-reviewed published literature on snow leopard
population estimation. Metadata analysis showed estimates of snow leopard density
to be a negative exponential function of area, suggesting that study areas have generally
been too small for accurate density estimation, and sampling has often been
biased towards the best habitats. Published studies are restricted to six of the
12 range countries, covering only 0.3�0.9% of the presumed global range of the
species. Re-sampling of camera trap data from a relatively large study site
(c.1684 km2) showed that small-sized study areas together with a bias towards
good quality habitats in existing studies may have overestimated densities by up to
five times. We conclude that current information is biased and inadequate for generating
a reliable global population estimate of snow leopards. To develop a rigorous
and useful baseline and to avoid pitfalls, there is an urgent need for
(a) refinement of sampling and analytical protocols for population estimation of
snow leopards (b) agreement and coordinated use of standardized sampling protocols
amongst researchers and governments across the range, and (c) sampling
larger and under-represented areas of the snow leopard's global range.
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