A heterothermic spectrum in hummingbirds

Many endotherms use torpor, saving energy by a controlled reduction of their body temperature and metabolic rate. Some species (e.g., arctic ground squirrels, hummingbirds) enter deep torpor, dropping their body temperatures by 23-37°C, while others can only enter shallow torpor (e.g., pigeons, 3-10°C reductions). However, deep torpor in mammals can increase predation risk (unless animals are in burrows or caves), inhibit immune function, and result in sleep deprivation, so even for species that can enter deep torpor, facultative shallow torpor might help balance energy savings with these potential costs. Deep torpor occurs in three avian orders, but the trade-offs of deep torpor in birds are unknown. Although the literature hints that some bird species (mousebirds and perhaps hummingbirds) can use both shallow and deep torpor, little empirical evidence of such an avian heterothermy spectrum within species exists. We infrared imaged three hummingbird species that are known to use deep torpor, under natural temperature and light cycles, to test if they were also capable of shallow torpor. All three species used both deep and shallow torpor, often on the same night. Depending on the species, they used shallow torpor for 5-35% of the night. The presence of a heterothermic spectrum in these bird species indicates a capacity for fine-scale physiological and genetic regulation of avian torpid metabolism.

Facultative variation across a shallow to deep torpor spectrum in hummingbirds

Many small endotherms use torpor, saving energy by a controlled reduction of their body temperature and metabolic rate. Some species (e.g. arctic ground squirrels, hummingbirds) enter deep torpor, dropping their body temperatures by 23-37 °C, while others can only enter shallow torpor (e.g., pigeons, 3-10 °C reductions). However, deep torpor in mammals can increase predation risk (unless animals are in burrows or caves), inhibit immune function, and result in sleep deprivation, so even for species that can enter deep torpor, facultative shallow torpor might help balance energy savings with these potential costs. Deep torpor occurs in three avian orders. Although the literature hints that some bird species can use both shallow and deep torpor, little empirical evidence of such an avian torpor spectrum exists. We infrared imaged three hummingbird species that are known to use deep torpor, under natural temperature and light cycles, to test if they were also capable of shallow torpor. All three species used both deep and shallow torpor, often on the same night. Depending on the species, they used shallow torpor for 5-35% of the night. The presence of a bird torpor spectrum indicates a capacity for fine-scale physiological and genetic regulation of avian torpid metabolism.

Landscape-scale habitat associations of small mammals on the western coast of Hudson Bay

Availability of suitable habitat affects the distribution and abundance of Arctic fauna, influencing how species respond to climate change and disturbance from resource extraction in the region. We surveyed Arctic ground squirrels (Urocitellus parryii Richardson, 1825) using distance sampling transects and concurrently counted microtine rodent burrows. Abundance of Arctic ground squirrels and microtine burrows was positively correlated with terrain ruggedness. Microtine burrows were more abundant inland and in areas with freshwater, while Arctic ground squirrels were more often found at low elevation without freshwater. Arctic ground squirrel abundance was positively related to the normalized difference water index, a proxy for vegetation water content, while microtine burrows were weakly correlated with the normalized difference vegetation index. Our study highlights the habitat associations of ecologically significant small mammals in an underrepresented Arctic study area.