The stable isotope composition of carbon and nitrogen in feces can be a useful tool for reconstructing diet. To examine whether the isotopic composition of feces reflect those of diet, we determined the fractionation of 15N and 13C along the digestive tracts of several species of small mammals. There were significant differences in the δ15N values of digesta in different compartments of the gastrointestinal (GI) tract, with consistent enrichment of 15N in the stomach, intestine, and cecum, and the depletion of 15N in the colon (i.e., feces). Although feces had lower δ15N values than digesta in the cecum, feces of small mammals were significantly more enriched in 15N (by ~2.5‰) than diet. The mechanisms causing this enrichment in the GI tract may arise from the operation of different biochemical pathways within the different GI compartments. The stable carbon isotope composition of digesta in small mammals were similar along the GI tract, but the δ13C values of digesta and feces were significantly lower than reported previously for large ungulates (–3.5‰ vs. –0.5‰). The δ15N and δ13C values of feces did not directly reflect the isotopic compositions of these mammals’ diet. Our data offer evidence for variations in isotopic discrimination effects. This variation can probably be ascribed to metabolism of different body sizes of mammals and the complexities linked with digestive physiology of herbivores.
We assessed patterns and energetic consequences of different overwintering strategies, torpor, and social thermoregulation in the striped skunk (Mephitis mephitis) under natural ambient temperature and photoperiod. Striped skunks entered spontaneous daily torpor, with the lowest torpid body temperature (T(b)) reaching 26.0 degrees C, the lowest recorded T(b) for a carnivore. Patterns of daily torpor differed between solitary and grouped skunks: all solitary skunks regularly entered daily torpor, but only some individuals in communal dens employed torpor. When they did, it was shallow and infrequent. Solitary skunks entered torpor on average 50 times (in 120 d) compared with 6 times for grouped skunks. During torpor, solitary skunks had average minimum T(b) of 26.8 degrees C and bout duration of 7.8 h, whereas grouped skunks had average minimum T(b) of 30.9 degrees C and bout duration of 5.4 h. Torpor by solitary skunks occurred during their activity phase, but grouped skunks' shallow torpor bouts were restricted to their diurnal resting phase. On average, grouped skunks experienced lower percent daily fat loss, and they emerged in spring with higher percent body fat of 25.5%. In contrast, solitary skunks emerged in spring with only 9.3% body fat. In conclusion, the use of daily torpor and social thermoregulation in northern populations of striped skunks represent two strikingly different mechanisms to minimize energetic costs and increase individual fitness in response to unfavorable environmental conditions.
1. Predicting the spatial pattern of disease risk in wild animal populations is important for implementing effective control programmes. We developed a risk model predicting the probability that a deer harvested in a wild population was chronic wasting disease positive (CWD+) and evaluated the importance of landscape connectivity based on deer movements. 2. We quantified landscape connectivity from deer 'resistance' to move across the landscape similar to the flow of electrical current across a hypothetical electronic circuit. Resistance values to deer movement were derived as the inverse of step selection function values constructed using movement data from GPS-collared deer. 3. The top CWD risk model indicated risk increased over time was higher among mule deer Odocoileus hemionus than white-tailed deer Odocoileus virginianus, males than females, and was greater in areas with high stream density and abundant agriculture. A metric of connectivity derived from mule deer movements outperformed models including Euclidean distance, with high connectivity being associated with high CWD risk. 4. The CWD risk model was a good predictor of CWD occurrence among an independent set of surveillance data collected in subsequent years. 5. Synthesis and applications. We found that landscape connectivity was a major contributor to the spatial pattern of chronic wasting disease (CWD) risk on a heterogeneous landscape. For this reason, future disease surveillance programmes and models of disease spread should consider landscape connectivity. In the aspen parkland ecosystem, we recommend managers focus surveillance and control efforts along river valleys surrounded by agriculture where mule deer abound, because of the high risk of CWD infection. Fig. 4. (a) Chronic wasting disease (CWD) risk weighted by species and sex composition within wildlife management unit 730 in Alberta, and (b) forest/shrub cover, streams and agriculture within 730, where streams and agriculture are covariates in the CWD risk model.
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