No description available.

No description available.

Because little is known about juvenile American White Pelicans (Pelecanus erythrorhynchos) this study was conducted to gather more information on disease, general ecology and growth of American White Pelicans from hatching to fledging. In July 2011, American White Pelican regurgitate samples from North and South Dakota sub-colonies were collected/analyzed in preparation for a captive trial. Nutrient content compared between the colonies was found to be significantly different. Concentrations of Immunoglobulin Y and A in regurgitate samples were significantly different between colonies. A captive trial began 29 May 2012 and ended 30 July 2012, in which 16 American White Pelicans were hand raised from hatching to fledging. During the captive trial, various growth parameters, intake and fecal output were examined to determine the effect of the parasite Bolbophorus damnificus in 8 infected and 8 non-infected (parasite free) pelicans. Growth data collected on B. damnificus infected (n = 8) American White Pelicans was compared to previously mentioned parasiteree pelicans (n = 8) to determine effects of the parasite. There were no differences between groups for culmen length (P= 0.214), tarsal length (P = 0.306), body weight (P = 0.884) or intake (P = 0.963). There was also no effect of the parasite on body temperature. Towards the end of the captive trial, several pelicans both on (n = 16) and off (n = 11) trial became naturally infected with West Nile Virus. Clinical symptoms ranged from lethargy and/or wing droop to total paralysis. Progression of disease is detailed in two well-defined case studies with additional information included on clinical signs, physiological parameters, and a review of the pathology of disease for other infected birds.

Moist-soil wetlands that are seasonally flooded provide important habitats for waterfowl in the Mississippi Alluvial Valley (MAV). These wetlands often contain tall and dense vegetation that may constrain waterfowl use before natural openings form. During winters 2006–2009, I estimated abundances of waterbirds, seeds and tubers, and invertebrates in response to autumn, prelooding treatments of light disking, mowing, and no manipulation (control) of vegetation in 26 moist-soil wetlands in the MAV. Seeds and tubers were most abundant in control and mowed plots in late autumn. Decomposition was least and invertebrate abundance was greatest in control plots during winter. Dabbling ducks were most abundant in mowed and disked plots during winter. Lightly disked plots contained ~30% fewer seeds and tubers than mowed and control plots. In late winter, ~260 kg[dry]/ha of seeds and tubers remained among mowed, disked, and control plots. Therefore, autumn mowing of robust moist-soil vegetation can be used to create an interspersion of emergent vegetation and open water attractive to waterfowl and conserve waterfowl foods. Additionally, I identified 6 seed taxa that may not be used for food by dabbling ducks (i.e., Amaranthus spp., Cyperus odoratus, Eleocharis spp., Ipomoea spp., Jacquemontia tamnifolia, Sesbania herbacea) and estimated that removing these and other taxa not reported in diet literature in the MAV resulted in a ~31% reduction in estimated moist-soil food availability for ducks. In other experiments, I estimated that waterfowl reduced experimentally placed Japanese millet (Echinochloa frumentacea) to ~10 kg/ha and other natural seeds and tubers to ~170 kg/ha in experimental plots in mid-winter. However, waterfowl did not abandon wetlands or stop foraging when seed reduction ceased, suggesting residual abundances of seeds and tubers represented a food availability threshold (FAT). Using the median FAT value of 220 kg/ha from both experiments and removing 31% of seed mass that may not be consumed by dabbling ducks, results in a ~70% decrease in moist-soil seed availability in the MAV. Conservation planners should consider reducing the current estimates of seed and tuber availability and recommend increasing active management or implementation of additional managed, moist-soil wetlands in the MAV.

Endotherms living in cold environments must pay the energetic cost of maintaining a high core body temperature. This cost can be potentially alleviated by an important yet often overlooked mechanism: “activity-thermoregulatory heat substitution” (i.e., the use of the heat generated by active skeletal muscles to replace heat that would have been generated by thermogenesis). While substitution has been documented numerous times, the extent of individual variation in substitution has never been quantified. I used a respirometry cage system to repeatedly measure substitution through the concomitant monitoring of metabolic rate (MR) and locomotor activity in 46 female white-footed mice (Peromyscus leucopus) in neutral and cold ambient temperatures. I took a total of 117 measures of substitution by quantifying the difference in the slope of the relationship between MR and locomotor activity speed at two different ambient temperatures. Consistency repeatability (±se) of substitution was 0.313±0.131 – hence, about a third of the variation in substitution occurs at the among-individual level. Including key morphological traits such as trunk surface area, tail mass, heart mass, and body length accounted for the majority of the among-individual variation, suggesting that I have successfully identified traits underlying individual differences in substitution. Overall, my results show that substitution is repeatable and hence might potentially be subject to selection. Future studies should test if substitution conveys fitness advantages directly (by providing energetically cheaper activity which in turn can be utilized for reproduction), or indirectly (i.e., driven by individual differences in morphology). Future studies should also test if there is a trade-off between substitution and dry heat transfer (a thermoregulatory mechanism essential for preventing hyperthermia).

No description available.

No description available.

No description available.

No description available.

Insectivorous bats alter relative use of metabolic substrates to match requirements of their activities, including energetically expensive flight. The “fasting while foraging” hypothesis states that the metabolic demands of flight often exceed energy intake while foraging, hence bats may metabolize fat stores (especially early in the night) to power flight with ketones, a byproduct of the normal oxidation of fatty acids. Previous studies in bats have found increases in the plasma ketone ß-hydroxybutyrate following food consumption paired with or without flight. However, no study has explored whether increases in plasma ß-hydroxybutyrate occur following flight without food consumption. We used metabolite analysis to examine changes in plasma ß-hydroxybutyrate as a function of flight duration in 2 groups (fall and spring) of captive big brown bats (Eptesicus fuscus). We fasted bats for 12 hours prior to flight (exercise treatment) or rest (control), and then collected interfemoral vein blood. Exercise activity was quantified as flight time. For the Fall group, we collected three rest samples and one flight sample. Results for the Fall group were variable; interpretation of data patterns for this group may be complicated by changes in metabolism that occur in the fall when bats physiologically prepare for hibernation. To control for seasonal effects, we tested a second group of bats in the spring, collecting two rest and three flight samples. We found a positive correlation between flight duration and levels of plasma ß-hydroxybutyrate in the Spring group, which supports the fasting while foraging hypothesis. / Thesis / Master of Science (MSc) / The “fasting while foraging” hypothesis states that the metabolic demands of flight can exceed energy intake from recently consumed prey items, so insectivorous bats may metabolize fat stores (especially early in the night) to power flight with ketones, a byproduct of the normal oxidation of fatty acids. Previous studies in bats have found increases in the plasma ketone ß-hydroxybutyrate following food consumption, but no study has explored whether increases in plasma ß-hydroxybutyrate occur following flight without food consumption. We collected and analyzed blood to examine changes in plasma ß-hydroxybutyrate following different flight durations in big brown bats. We explored both seasonal and captivity effects. To explore seasonal effects, we sampled blood from bats in the fall and the spring, times that are biologically significant to big brown bats. The spring is when bats move out of torpor, a form of hibernation, into an active state and the fall is when bats are preparing for entering into torpor. To explore captivity effects, we sampled blood from bats recently introduced to or established to captivity. Bats were fasted for 12 hours prior to flight (exercise treatment) or rest (control), and then blood was collected. We characterized exercise using flight time. We found that plasma ß-hydroxybutyrate increased after longer flight durations, which supports the fasting while foraging hypothesis.