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| Author | Chetri, M, Odden, M., Sharma, K., Flagstad, O., Wegge, P | ||||
| Title | Estimating snow leopard density using fecal DNA in a large landscape in north-central Nepal | Type | Journal Article | ||
| Year | 2019 | Publication | Global Ecology and Conservation | Abbreviated Journal | |
| Volume | Issue  |
17 | Pages | 1-8 | |
| Keywords | Panthera uncia, Density, Annapurna-Manaslu landscape, Noninvasive, Spatial scale | ||||
| Abstract | Although abundance estimates have a strong bearing on the conservation status of a species, less than 2% of the global snow leopard distribution range has been sampled systematically, mostly in small survey areas. In order to estimate snow leopard density across a large landscape, we collected 347 putative snow leopard scats from 246 transects (490 km) in twenty-six 5 5km sized sampling grid cells within 4393 km2 in Annapurna- Manaslu, Nepal. From 182 confirmed snow leopard scats, 81 were identified as belonging to 34 individuals; the remaining were discarded for their low (<0.625) quality index. Using maximum likelihood based spatial capture recapture analysis, we developed candidate model sets to test effects of various covariates on density and detection of scats on transects. The best models described the variation in density as a quadratic function of elevation and detection as a linear function of topography. The average density estimate of snow leopards for the area of interest within Nepal was 0.95 (SE 0.19) animals per 100 km2 (0.66e1.41 95% CL) with predicted densities varying between 0.1 and 1.9 in different parts, thus highlighting the heterogeneity in densities as a function of habitat types. Our density estimate was low compared to previous estimates from smaller study areas. Probably, estimates from some of these areas were inflated due to locally high abundances in overlap zones (hotspots) of neighboring individuals, whose territories probably range far beyond study area borders. Our results highlight the need for a large-scale approach in snow leopard monitoring, and we recommend that methodological problems related to spatial scale are taken into account in future snow leopard research. |
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| Notes | Approved | no | |||
| Call Number | SLN @ rakhee @ | Serial | 1478 | ||
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| Author | Pollock, R.V.; Carmichael, L.E. | ||||
| Title | Use of modified live feline panleukopenia virus vaccine to immunize dogs against canine parvovirus | Type | Journal Article | ||
| Year | 1983 | Publication | Am J Vet Res | Abbreviated Journal | |
| Volume | 44 | Issue |
2 | Pages | 169-175 |
| Keywords | Animal; Antibodies; Viral; biosynthesis; Dog; Diseases; microbiology; prevention; control; Dogs; Dose; Response; Relationship; Immunologic; Parvoviridae; immunology; Parvovirus; Feline; growth; development; Support; Non-U.S.Gov't; Vaccines; Attenuated; Virus; veterinary; Replication; browse; 350 | ||||
| Abstract | Modified live feline panleukopenia virus (FPLV) vaccine protected dogs against canine parvovirus (CPV) infection. However, unlike the long- lived (greater than or equal to 20-month) immunity engendered by CPV infection, the response of dogs to living FPLV was variable. Doses of FPLV (snow leopard strain) in excess of 10(5.7) TCID50 were necessary for uniform immunization; smaller inocula resulted in decreased success rates. The duration of immunity, as measured by the persistence of hemagglutination-inhibiting antibody, was related to the magnitude of the initial response to vaccination; dogs with vigorous initial responses resisted oronasal CPV challenge exposure 6 months after vaccination, and hemagglutination-inhibiting antibodies persisted in such dogs for greater than 1 year. Limited replication of FPLV in dogs was demonstrated, but unlike CPV, the feline virus did not spread to contact dogs or cats. Adverse reactions were not associated with living FPLV vaccination, and FPLV did not interfere with simultaneous response to attenuated canine distemper virus. | ||||
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| ISSN | 0002-9645 | ISBN | Medium | ||
| Area | Expedition | Conference | |||
| Notes | Document Type: eng | Approved | no | ||
| Call Number | SLN @ rana @ 69 | Serial | 784 | ||
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| Author | Janecka, J. E., Jackson, R., Munkhtsog, B., Murphy, W. J. | ||||
| Title | Characterization of 9 microsatellites and primers in snow leopards and a species-specific PCR assay for identifying noninvasive samples | Type | Journal Article | ||
| Year | 2014 | Publication | Conservation Genetic Resource | Abbreviated Journal | |
| Volume | 6 | Issue |
2 | Pages | 369:373 |
| Keywords | Microsatellites,Cytochrome b, Snow Leopard, Noninvasive genetics, Individual identification | ||||
| Abstract | Molecular markers that can effectively identify noninvasively collected samples and provide genetic information are critical for understanding the distribution, status, and ecology of snow leopards (Panthera uncia). However, the low DNA quantity and quality in many noninvasive samples such as scats makes PCR amplification and genotyping challenging. We therefore designed primers for 9 microsatellites loci previously isolated in the domestic cat (Felis catus) specifically for snow leopard studies using noninvasive samples. The loci showed moderate levels of variation in two Mongolian snow leopard populations. Combined with seven other loci that we previously described, they have sufficient variation (He = 0.504, An = 3.6) for individual identification and population structure analysis. We designed a species species specific PCR assay using cytochrome b for identification of unknown snow leopard samples. These molecular markers facilitate in depth studies to assess distribution, abundance, population structure, and landscape connectivity of this endangered species. endangered species |
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| Notes | Approved | no | |||
| Call Number | SLN @ rakhee @ | Serial | 1427 | ||
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| Author | Janecka, J. E., Jackson, R., Munkhtsog, B., Murphy, W. J. | ||||
| Title | Characterization of 9 microsatellites and primers in snow leopards and a species-specific PCR assay for identifying noninvasive samples | Type | Journal Article | ||
| Year | 2014 | Publication | Conservation Genetic Resource | Abbreviated Journal | |
| Volume | 6 | Issue |
2 | Pages | 369:373 |
| Keywords | Microsatellites,Cytochrome b, Snow Leopard, Noninvasive genetics, Individual identification | ||||
| Abstract | Molecular markers that can effectively identify noninvasively collected samples and provide genetic information are critical for understanding the distribution, status, and ecology of snow leopards (Panthera uncia). However, the low DNA quantity and quality in many noninvasive samples such as scats makes PCR amplification and genotyping challenging. We therefore designed primers for 9 microsatellites loci previously isolated in the domestic cat (Felis catus) specifically for snow leopard studies using noninvasive samples. The loci showed moderate levels of variation in two Mongolian snow leopard populations. Combined with seven other loci that we previously described, they have sufficient variation (He = 0.504, An = 3.6) for individual identification and population structure analysis. We designed a species species specific PCR assay using cytochrome b for identification of unknown snow leopard samples. These molecular markers facilitate in depth studies to assess distribution, abundance, population structure, and landscape connectivity of this endangered species. |
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| Area | Expedition | Conference | |||
| Notes | Approved | no | |||
| Call Number | SLN @ rakhee @ | Serial | 1428 | ||
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| Author | Roth, T.L.; Armstrong, D.L.; Barrie, M.T.; Wildt, D.E. | ||||
| Title | Seasonal effects on ovarian responsiveness to exogenous gonadotrophins and successful artificial insemination in the snow leopard (Uncia uncia) | Type | Journal Article | ||
| Year | 1997 | Publication | Reprod Fertil Dev | Abbreviated Journal | |
| Volume | 9 | Issue |
3 | Pages | 285-295 |
| Keywords | Animal; Carnivora; anatomy; histology; Blood; physiology; Estradiol; Female; Gonadotropins; administration; dosage; pharmacology; Chorionic; Equine; Human; Insemination; artificial; methods; veterinary; Laparoscopy; Male; Oocytes; cytology; Ovary; drug; effects; Ovulation; Induction; Pregnancy; Progesterone; Seasons; Support; Non-U.S.Gov't; browse; non; us; gov't; government; 400 | ||||
| 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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| Series Volume | Series Issue | Edition | |||
| ISSN | 1031-3613 | ISBN | Medium | ||
| Area | Expedition | Conference | |||
| Notes | Document Type: eng | Approved | no | ||
| Call Number | SLN @ rana @ 325 | Serial | 830 | ||
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| Author | Rothschild, B.M.; Rothschild, C.; Woods, R.J. | ||||
| Title | Inflammatory arthritis in large cats: An expanded spectrum of spondyloarthropathy | Type | Journal Article | ||
| Year | 1998 | Publication | Journal of Zoo and Wildlife Medicine | Abbreviated Journal | |
| Volume | 29 | Issue |
3 | Pages | 279-284 |
| Keywords | Acinonyx-jubatus; cheetah; Felidae; Felis-concolor; mountain-lion; Felis-pardalis; ocelot; Panthera-leo; African-lion; Panthera-onca; jaguar; Panthera-pardus; leopard; Panthera-tigris; tiger; Panthera-uncia; snow-leopard; snow leopard; Acinonyx; jubatus; felis; concolor; mountain; lion; pardalis; panthera; leo; african; onca; pardus; tigris; uncia; browse; 1240 | ||||
| Abstract | Spondyloarthropathy was documented for the first time in 14 (3.7%) of 386 large cats, affecting eight species belonging to three genera. The limited distribution of joint erosions, associated with spine and sacroiliac joint pathology, was indistinguishable from that occurring in humans with spondyloarthropathy of the reactive type. This form of inflammatory arthritis is almost twice as common as osteoarthritis (for felids as a whole), and animal well-being may be enhanced by its recognition and by initiation of specific treatment. | ||||
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| Notes | Document Type: English | Approved | no | ||
| Call Number | SLN @ rana @ 353 | Serial | 832 | ||
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| Author | Roth, T.L.; Howard, J.G.; Donoghue, A.M.; Swanson, W.F.; Wildt, D.E. | ||||
| Title | Function and culture requirements of snow leopard (Panthera uncia) spermatozoa in vitro | Type | Journal Article | ||
| Year | 1994 | Publication | J Reprod Fertil | Abbreviated Journal | |
| Volume | 101 | Issue |
3 | Pages | 563-569 |
| Keywords | Animal; Carnivora; physiology; Cell; survival; Cells; Cultured; Comparative; study; Culture; Media; Female; Male; Pentoxifylline; Sperm; Motility; Ovum; Interactions; Spermatozoa; cytology; Support; Non-U.S.Gov't; U.S.Gov't; P.H.S.; browse; non; us; gov't; government; 190 | ||||
| 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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| ISSN | 0022-4251 | ISBN | Medium | ||
| Area | Expedition | Conference | |||
| Notes | Document Type: eng | Approved | no | ||
| Call Number | SLN @ rana @ 253 | Serial | 828 | ||
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| Author | Ali, S.M. | ||||
| Title | The Cats of India | Type | Journal Article | ||
| Year | 1990 | Publication | Myforest | Abbreviated Journal | |
| Volume | 26 | Issue |
3 | Pages | 275-291 |
| Keywords | lion; clouded-leopard; cheetah; tiger; leopard; snow-leopard; India; Panthera-leo; Neofelis-nebylosa; Acinonyx-jubatus; Panthera-tigris; Panthera-pardus; Panthera-uncia; behavior; ecology; snow leopard; browse; panthera; uncia; pardus; clouded; leo; neofelis; nebylosa; ancinonyx; jubatus; 820 | ||||
| Abstract | Describes the range, behaviour and ecology of lion Panthera leo, tiger P. tigris, leopard P. pardus, snow leopard P. uncia, clouded leopard Neofelis nebylosa and cheetah Acinonyx jubatus. -P.J.Jarvis | ||||
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| Notes | Approved | no | |||
| Call Number | SLN @ rana @ 144 | Serial | 59 | ||
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| Author | Brown, J.L.; Wasser, S.K.; Wildt, D.E.; Graham, L.H. | ||||
| Title | Comparative Aspects of Steroid Hormone Metabolism and Ovarian Activity in Felids, Measured Noninvasively in Feces | Type | Journal Article | ||
| Year | 1994 | Publication | Biol Reprod | Abbreviated Journal | |
| Volume | 51 | Issue |
4 | Pages | 776-786 |
| Keywords | Animal; Carbon; Radioisotopes; Carnivora; Cats; Chromatography; High; Pressure; Liquid; Comparative Study; Estradiol; metabolism; Estrone; feces; chemistry; Female; Ovary; physiology; Pregnancy; Progesterone; Pseudopregnancy; Support; Non-U.S.Gov't; browse; non; government; gov't; us; 170 | ||||
| Abstract | Noninvasive fecal assays were used to study steroid metabolism and ovarian activity in several felid species. Using the domestic cat (Felis catus) as model, the excretory products of injected [14C]estradiol (E2) and [14C]progesterone (P4) were determined. Within 2 days, 97.0 +/- 0.6% and 96.7 +/- 0.5% of recovered E2 and P4 radioactivity, respectively, was found in feces. E2 was excreted as unconjugated estradiol and estrone (40%) and as a non-enzyme- hydrolyzable conjugate (60%). P4 was excreted primarily as non-enzyme- hydrolyzable, conjugated metabolites (78%) and as unconjugated pregnenolone epimers. A simple method for extracting fecal steroid metabolites optimized extraction efficiencies of the E2 and P4 excretion products (90.1 +/- 0.8% and 87.2 +/- 1.4%, respectively). Analysis of HPLC fractions of extracted fecal samples from the radiolabel-injected domestic cats revealed that E2 immunoreactivity coincided primarily with the unconjugated metabolized [14C]E2 peak, whereas progestogen immunoreactivity coincided with a single conjugated epimer and multiple unconjugated pregnenolone epimers. After HPLC separation, similar immunoreactive E2 and P4 metabolite profiles were observed in the leopard cat (F. bengalensis), cheetah (Acinonyx jubatus), clouded leopard (Neofelis nebulosa), and snow leopard (Panthera uncia). Longitudinal analyses demonstrated that changes in fecal E2 and P4 metabolite concentrations reflected natural or artificially induced ovarian activity. For example, severalfold increases in E2 excretion were associated with overt estrus or exogenous gonadotropin treatment, and elevated fecal P4 metabolite concentrations occurred during pregnant and nonpregnant (pseudopregnant) luteal phases. Although overall concentrations were similar, the duration of elevated fecal P4 metabolites during pseudopregnancy was approximately half that observed during pregnancy. In summary, steroid metabolism mechanisms appear to be conserved among these physically diverse, taxonomically related species. Results indicate that this hormone-monitoring approach will be extremely useful for elucidating the hormonal regulatory mechanism associated with the reproductive cycle, pregnancy, and parturition of intractable and endangered felid species. | ||||
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| ISSN | 0006-3363 | ISBN | Medium | ||
| Area | Expedition | Conference | |||
| Notes | Document Type: eng | Approved | no | ||
| Call Number | SLN @ rana @ 251 | Serial | 198 | ||
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| Author | Johnston, L.A.; Donoghue, A.M.; O'Brien, S.J.; Wildt, D.E. | ||||
| Title | Rescue and maturation in vitro of follicular oocytes collected from nondomestic felid species | Type | Journal Article | ||
| Year | 1991 | Publication | Biol Reprod | Abbreviated Journal | |
| Volume | 45 | Issue |
6 | Pages | 898-906 |
| Keywords | Animal; Carnivora; anatomy; histology; physiology; Cells; Cultured; Female; Fertilization; Vitro; inVitro; Male; Oocytes; cytology; growth; development; ovarian; Follicle; Spermatozoa; Support; Non-U.S.Gov't; U.S.Gov't; P.H.S.; browse; non; us; gov't; government; 230 | ||||
| Abstract | The potential for rescuing immature oocytes from the ovaries of females of rare felid species which die or undergo medical ovariohysterectomy was evaluated. Ovaries were recovered from 13 species representing 35 individuals in good-to-poor health. Although the majority of females were 10 yr of age or older and in fair-to-poor health, a total of 846 oocytes were recovered of which 608 (71.9%) were classified as fair-to- excellent quality. One hundred of these oocytes were used for initial maturation classification and as parthogenetic controls. Overall, of the 508 fair-to-excellent quality oocytes placed in culture, 164 (32.3%) matured to metaphase II in vitro. For species in which 3 or more individuals yielded oocytes, mean oocyte maturation rates were as follows: 36.2%, tiger; 27.9% leopard; and 8.3%, cheetah. In vitro insemination of oocytes resulted in fertilization (2 polar bodies, 2 pronuclei, or cleavage) rates of 9.1% to 28.6% (leopard) using homologous fresh spermatozoa and 4.0% (lion) to 40.0% (puma) using homologous frozen-thawed spermatozoa. Inseminations using heterologous (domestic cat) spermatozoa also resulted in fertilized oocytes in the tiger, leopard, snow leopard, puma, serval, and Geoffroy's cat (range in fertilization rate, 5.0% for leopard to 46.2% for puma). Cleaved embryos resulted from the insemination of leopard oocytes with homologous sperm (n = 1 embryo) and puma oocytes with domestic cat sperm (n = 3 embryos). These results demonstrate that immature ovarian oocytes from rare felid species can be stimulated to mature in vitro despite an excision-to-culture interval as long as 36 h.(ABSTRACT TRUNCATED AT 250 WORDS) | ||||
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| ISSN | 0006-3363 | ISBN | Medium | ||
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| Notes | Document Type: eng | Approved | no | ||
| Call Number | SLN @ rana @ 172 | Serial | 503 | ||
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