Abstract: Against a background of recovering large carnivore populations in Norway, and many other areas of Europe, it is becoming increasingly important to develop methods to monitor their populations. A variety of parameters can monitored depending on objectives. These parameters include: presence/absense, distribution, population trend indices, minimum counts, statistical estimates of population size, reproductive parameters and health/condition. Three broad categories of monitoring techniques can be recognised each with increasing levels of fieldwork required. The first category includes those techniques that do not require original fieldwork. The second category involves fieldwork, but where individually recognisable carnivores are not available. The third category includes methods where fieldwork has recognisable individuals available. Different mehtods tend to have been used for different species, mainly because of limitations imposed by the different species' ecology. The most precise estimates of population size have been obtained in research projects with relatively small study sites and with the help of radio-telemetry. However, it may be difficult, or impossible, to apply these methods over large monitoring areas. Therefore, in terms of practical management, a combination of minimum counts, supported by an independent index may be more useful than statistical population estimates. All methods should be subject to a careful design process, and power analysis should be conducted to determine the sensitivity of the method to detect changes.
Based on the review of over 200 papers and reports we recommend a package of complementary monitoring methods for brown bear, wolverine, lynx and wolf in Norway. These include the use of observations from the public and reports of predation on livestock to determine broad patterns of distribution, and an index based on hunter observations per hunting day, for all four species. Minimum counts of reproductive units, natal dens, family groups, and packs, should be obtained from snow-tracking for wolverines, lynx and wolves respectively. In addition a track-count index should be obtained for wolverines and lynx. As much data as possible should be obtained of lynx and wolvereines killed in the annual harvest. Brown bears will be difficult to monitor without the use of radio-telemetry, therfore they may require periodic telemetry based, mark-recapture studies. Such a program can easily be constructed within existing central and regional wildlife management structures, but will require extensive involvement from hunters.

Abstract: A full hierarchic system of mammal fauna in the USSR and CIS countries, list of synonyms, comments on taxonomy, and information about geographical distribution are given. Genus Uncia Gray, 1854 includes one species U. uncia (Schreber, 1776) distributed in highlands (up to 5,000 m) of Central Asia (Tibet, Pamir, Tien-Shan, Altai). Synonyms: irbis.

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.

Abstract: The purpose of this study was to determine the molecular basis for a relative deficiency in the cat of cytosolic arylamine N- acetyltransferase (NAT), an enzyme family that is important in the metabolism of xenobiotics and that normally consists of at least two related enzymes, NAT1 and NAT2. N-acetyltransferase in feline liver showed high affinity (mean Km = 2.1 microM) for p-aminobenzoic acid, an NAT1 selective substrate in humans and rabbits, but showed a very poor affinity (mean Km > 10 mM) for sulfamethazine, an NAT2 selective substrate in humans and rabbits. Immunoreactive N-acetyltransferase was detected in feline liver, bladder and colon using an NAT1-specific antipeptide antibody, but was not detected in any tissues using an NAT2- specific antibody. Southern blot analysis of genomic DNA demonstrated a single band in domestic cats using each of six restriction digests; single bands were also found on Southern blot analysis of six wild felids. The deduced amino acid sequence of the central portion of feline N-acetyltransferase, obtained by polymerase chain reaction amplification in both domestic cats and seven wild felids (lion, tiger, lynx, snow leopard, bobcat, Asian leopard cat and cheetah), contained three residues, Phe125, Arg127, and Tyr129, which determine NAT1-like substrate specificity in humans. These results support the conclusion that cytosolic arylamine N-acetylation activity is low in the cat because of the presence of a single N-acetyltransferase that has substrate specificity, immunogenicity and sequence characteristics similar to human NAT1, and that the unusual presence of only a single N- acetyltransferase gene appears to be a family wide trait shared by other felids.