12 research outputs found

    Aerobic and anaerobic energy expenditure during rest and activity in montane Bufo b. boreas and Rana pipiens

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    The relations of standard and active aerobic and anaerobic metabolism and heart rate to body temperature ( T b ) were measured in montane groups of Bufo b. boreas and Rana pipiens maintained under field conditions. These amphibians experience daily variation of T b over 30°C and 23°C, respectively (Carey, 1978). Standard and active aerobic and anaerobic metabolism, heart rate, aerobic and anaerobic scope are markedly temperature-dependent with no broad plateaus of thermal independence. Heart rate increments provide little augmentation of oxygen transport during activity; increased extraction of oxygen from the blood probably contributes importantly to oxygen supply during activity. Development of extensive aerobic capacities in Bufo may be related to aggressive behavior of males during breeding. Standard metabolic rates of both species are more thermally dependent than comparable values for lowland relatives. Thermal sensitivity of physiological functions may have distinct advantages over thermally compensated rates in the short growing season and daily thermal fluctuations of the montane environment.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/47726/1/442_2004_Article_BF00348070.pd

    Factors affecting body temperatures of toads

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    Factors influencing levels and rates of variation of body temperature ( T b ) in montane Bufo boreas boreas and in lowland Bufo boreas halophilus were investigated as an initial step toward understanding the role of natural thermal variation in the physiology and energetics of these ectothermic animals. Body temperatures of boreas can vary 25–30° C over 24-h periods. Such variation is primarily due to both nocturnal and diurnal activity and the physical characteristics of the montane environment. Bufo boreas halophilus are primarily nocturnal except during breeding and are voluntarily active at body temperatures ranging between 10 and 25° C. Despite variation in T b encountered in the field, boreas select a narrow range of T b in a thermal gradient, averaging 23.5 and 26.2° C for fasted individuals maintained under field conditions or acclimated to 20° C, respectively. In a thermal gradient the mean T b of fasted halophilus acclimated to 20° C is 23.9° C. Skin color of boreas varies in the field from very dark to light. The dark skins absorb approximately 4% more radiation than the light ones. Light colored boreas should absorb approximately 5% more radiation than similarly colored halophilus . Evaporative water losses increase directly with skin temperatures and vapor pressure deficit in both subspecies. Larger individuals heat and cool more slowly than smaller ones. Calculation of an enery budget for boreal toads suggests that they could sit in direct sunlight for long periods without fatally overheating, providing the skin was continually moist.Peer Reviewedhttp://deepblue.lib.umich.edu/bitstream/2027.42/47722/1/442_2004_Article_BF00344732.pd

    Data from: Post-metamorphic carry-over effects of larval digestive plasticity

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    For animals with complex life cycles, conditions in the larval environment can have important effects that persist after metamorphosis. These carry-over effects may influence juvenile growth plasticity and have important fitness consequences. Small juvenile red-eyed treefrogs, Agalychnis callidryas, grow faster than larger ones. We examined to what extent this growth pattern is due to carry-over effects of intraspecific larval competition. In particular, we assessed larval gut plasticity and determined whether carry-over effects could persist given the extensive gut remodelling that occurs when herbivorous larvae transition to carnivorous juveniles. We reared larvae in mesocosms at low, medium and high densities and measured the size of both larval and juvenile guts, livers and fat bodies. We also monitored the timing of the onset of juvenile feeding post-metamorphosis and, after the onset of feeding, we measured intake rate and mean diet retention time. Finally, we measured juvenile metabolic rates to determine whether any organ size plasticity contributed to metabolic carry-over effects. Larval density had strong effects on larval morphology with higher densities increasing gut length and decreasing liver and fat body sizes. The effects of this plasticity carried over post-metamorphosis. High larval densities produced smaller juveniles with proportionately longer guts and extremely small livers and fat bodies. There were no apparent carry-over effects on size-specific metabolic rate. Differences in larval density were also associated with differences in post-metamorphic feeding. Small juveniles from high larval densities began feeding even before metamorphosis was complete, whereas large juveniles from low larval densities experienced a significant 2-week delay. Although juvenile body mass varied over threefold across treatments, once feeding was initiated, neither intake nor mean diet retention time scaled with body size. Overall, high larval densities produced small juveniles with very low lipid reserves that may have stimulated hyperphagia relative to larger juveniles. Longer guts carried over from the larval stage could facilitate this by allowing small juveniles to elevate intake without sacrificing diet retention time. Patterns of intake coupled with differences in the onset of feeding explain the size-dependent growth pattern previously reported in this and other species

    Seasonal changes in the diel surfacing behaviour of the bimodally respiring turtle Rheodytes leukops

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    The purpose of this study was to determine whether a relationship existed between the diel surfacing trends of the bimodally respiring freshwater turtle Rheodytes leukops and daily fluctuations in specific biotic and abiotic factors: The, diel surfacing behaviour of adult R. leukops was recorded over four consecutive seasons (Austral autumn 2000 - summer 2001) within Marlborough Creek, central Queensland, Australia, using pressure-sensitive time-depth recorders. Additionally, diurnal variations in water temperature and aquatic Po-2 level, as well as the turtle's behavioural state (i.e., active versus resting), were monitored. In autumn and summer, surfacing frequency increased significantly during the daylight hours, with peak levels normally occurring around dawn (0500-0700) and. dusk (1700-1900). However, no consistent diel surfacing trend was recorded, for the turtles in winter or spring, owing to considerable variation among individual R. leukops. Diurnal surfacing trends recorded for R. leukops in, autumn and summer are attributed to periods of increased activity (possibly associated with foraging) during the daylight hours and not to daily variations in water temperature or aquatic Po-2 level. Turtles generally remained at a depth greater than 1 m throughout the day, where the effect of diel fluctuations in water temperature,

    Tuataras and salamanders show that walking and running mechanics are ancient features of tetrapod locomotion

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    The lumbering locomotor behaviours of tuataras and salamanders are the best examples of quadrupedal locomotion of early terrestrial vertebrates. We show they use the same walking (out-of-phase) and running (in-phase) patterns of external mechanical energy fluctuations of the centre-of-mass known in fast moving (cursorial) animals. Thus, walking and running centre-of-mass mechanics have been a feature of tetrapods since quadrupedal locomotion emerged over 400 million years ago. When walking, these sprawling animals save external mechanical energy with the same pendular effectiveness observed in cursorial animals. However, unlike cursorial animals (that change footfall patterns and mechanics with speed), tuataras and salamanders use only diagonal couplet gaits and indifferently change from walking to running mechanics with no significant change in total mechanical energy. Thus, the change from walking to running is not related to speed and the advantage of walking versus running is unclear. Furthermore, lumbering mechanics in primitive tetrapods is reflected in having total mechanical energy driven by potential energy (rather than kinetic energy as in cursorial animals) and relative centre-of-mass displacements an order of magnitude greater than cursorial animals. Thus, large vertical displacements associated with lumbering locomotion in primitive tetrapods may preclude their ability to increase speed
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