Abstract: An extraction and assay procedure to measure fecal estradiol-17-beta and progestin concentrations in several cat species was developed and validated for use for noninvasive monitoring of ovarian function. Fecal samples were collected over a range of 3-20 months from female tigers (three), lions (three), snow leopards (three), cheetahs (two), caracals (two), and domestic cats (five). Samples were extracted with 90% methanol, lipids removed with petroleum ether, and the estradiol and progestins in the methanol measured by radioimmunoassay (RIA). High Performance Liquid Chromatography (HPLC) fractionation and subsequent RIA of the fractions indicated that the estradiol-17-beta antiserum cross-reacted primarily with estradiol-17-beta in the feces of lions and tigers and was assumed to be specific for estradiol-17-beta in the feces of other species as well. However, there were several immunoreactive compounds, presumably progesterone metabolites, excreted in the feces which varied both quantitatively and qualitatively among species. The behavior of tigers, lions, cheetahs, and caracals was visually monitored during the collection period and frequency of sexual behaviors was positively correlated with increases in fecal estradiol in all species observed. The mean fecal estradiol-17-beta peaks were as follows: tigers, 128.0 +- 13.1; lions, 186.0 +- 14.8; snow leopards, 136.7 +- 15.9; cheetahs, 140.9 +- 9.0; caracals, 24.5 +- 4.0; and domestic cats 158.9 +- 19.3 ng/gm. Fecal progestin concentrations rose significantly (P lt 0,001) only after breeding or during pregnancy and were as follows: tigers, 5.6 +- 0.6; lions, 1.9 +- 0.1; cheetahs, 8.4 +- 1.1; and caracals, 2.4 +- 0.4 mu-g/gm. Fecal progestins were elevated for one-half to two-thirds of the gestation length during presumed pseudopregnancy but remained elevated throughout successful pregnancies. These results suggest that ovarian function can be monitored noninvasively in the family Felidae by the measurement of fecal estradiol-17-beta and progestin concentrations.

Abstract: A high percentage of rare species in Central Asia experience limited conditions for distribution. Geographic centers with higher species diversity are generally constrained in terms of territory: they are formed when ranges overlap. But in Central Asia and along its borders with Russia, centers of biodiversity overlap at the very marginal edges of ranges. Central Asian species cross into Russian territory, where desert and steppe are replaced by thick forest. Here the northern borders of their ranges are sharply fragmented and isolated. Typical examples for Central Asia are the ranges of the cheetah (Acinonyx jubatus), Asian leopard (Panthera pardus caucasica), striped hyena (Hyaena hyaena), Bukhara deer (Census elaphus bactrianus), markhor (Capra falconeri), blue sheep (Pseudois nayauf) and argali (Ovis ammon). In Russia are the Altai subspecies of argali, the Siberian argali (O.a.ammon), the mountain goat (Capra sibirica), Mongolian gazelle (Procapra gutturosa), snow leopard (Uncia uncia), Pallas' cat (Felis manul), dhole (Cuon alpinus), grey marmot (Marmota baibacina), Mongolian marmot (M. sibirica) and tolai hare (Lepus tolai). Where the numbers o f individuals has fallen to extreme lows, the most effective mechanism for species survival may be supporting the integrity of ranges, in order to preserve population exchanges between neighboring groups. The geographic location of reserves and other protected territories is vitally important for the survival of Central Asian species, given the acute fragmentation of their ranges. These reserves should include significant, viable centers of population the key places. Wherever the creation of permanent protected territories is impossible, a new tactic must be found, such as introducing temporary limitations on the use of land for agriculture and hunting. But all protected territories, whether temporary or permanent, should be connected, forming a core and periphery. The marginal range areas must not be forgotten, if total protection of endangered populations is to be accomplished.

Abstract: The snow leopard Panthera uncia is one of the least studied felids in the world. Little is know about various aspects of the ecology of the snow leopard, which is cryptic in nature and found across 12 countries in Central Asia. Most research on snow leopards has been based on non-invasive methods such as sign surveys for presence (e.g. Jackson and Hunter 1996), scat analyses for diet (e.g. Chundawat and Rawat 1992; Oli et al., 2008, 2010) for population estimation, and studies based on human interviews (Mehta and Heinen 2001; Mishra and Bagchi 2006).
Despite this plethora of studies employing non-invasive techniques, several crucial questions about snow leopard ecology remain unanswered. Information about the animal’s home range, dispersal, corridors, pattern of habitat use, movement patterns, hunting frequency, behavior and intra – specific interactions is not available yet. In order to design population monitoring studies using camera traps or DNA analyses, one needs a good understanding of snow leopard ecology, including the home range and movement patterns (Williams et al., 2002). Telemetry is still the best available method and perhaps much less invasive than direct observations for studying the biology and ecology of cryptic animals.

Abstract: Twenty-five years ago, the snow leopard Uncia uncia, an endangered large cat, was eliminated from what is now Sagarmatha National Park (SNP). Heavy hunting pressure depleted that area of most medium-large mammals, before it became a park. After three decades of protection, the cessation of hunting and the recovery of wild ungulate populations, snow leopards have recently returned (four individuals). We have documented the effects of the return of the snow leopard on the population of its main wild prey, the Himalayan tahr Hemitragus jemlahicus, a 'near-threatened' caprin. Signs of snow leopard presence were recorded and scats were collected along a fixed trail (130 km) to assess the presence and food habits of the snow leopard in the Park, from 2004 to 2006. Himalayan tahr, the staple of the diet, had a relative occurrence of 48% in summer and 37% in autumn, compared with the next most frequent prey, musk deer Moschus chrysogaster (summer: 20%; autumn: 15%) and cattle (summer: 15%; autumn: 27%). In early summer, the birth rate of tahr (young-to-female ratio: 0.8-0.9) was high. The decrease of this ratio to 0.1-0.2 in autumn implied that summer predation concentrated on young tahr, eventually altering the population by removing the kid cohort. Small populations of wild Caprinae, for example the Himalayan tahr population in SNP, are sensitive to stochastic predation events and may be led to almost local extinction. If predation on livestock keeps growing, together with the decrease of Himalayan tahr, retaliatory killing of snow leopards by local people may be expected, and the snow leopard could again be at risk of local extinction. Restoration of biodiversity through the return of a large predator has to be monitored carefully, especially in areas affected by humans, where the lack of important environmental components, for example key prey species, may make the return of a predator a challenging event.