Abstract
Acute stressors such as capture and handling can elicit physiological responses in endothermic animals. One example of such a response is an increase in body temperature (Tb) commonly referred to as stress-induced hyperthermia (SIH). For species that employ torpor, typically an inactive state characterized by a controlled reduction in Tb and metabolic rate, a rapid increase in Tb could be advantageous, especially in the context of escape from predators. We quantified SIH in silver-haired bats (Lasionycteris noctivagans) because they readily enter torpor and often roost in exposed places where they could be vulnerable to predators. We tested the hypothesis that handling stress causes SIH in three separate contexts: a) during the nocturnal, active phase immediately following capture during flight, b) during the diurnal, inactive phase of normothermic bats, and c) during pronounced torpor immediately following exposure to cold ambient temperature. We used a standardized protocol during which Tb was measured (as rectal temperature) immediately upon handling and, again, several minutes later. We found that SIH occurred for inactive, normothermic bats held at a warm temperature. Surprisingly, however, handling stress caused a reduction in Tb for normothermic bats following the active, flight phase and, although in the opposite direction, this cooling rate was indistinguishable from the rate of SIH for normothermic bats during the rest phase. As expected, we observed a large change in Tb during rewarming from torpor following handling. This warming rate was greater than that previously reported in the literature for any heterothermic endotherm. Rapid rewarming by silver-haired bats could reflect their tendency to roost in relatively exposed locations that may be vulnerable to predators. This study provides new information on SIH in an under-studied group of animals and illustrates the need to evaluate the hypothesis that SIH and rewarming from torpor are influenced by predation risk and activity state.
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