No abstract

Mountain chickadees and juniper titmice from northern Utah were examined to determine metabolic and body-composition characteristics associated with seasonal acclimatization. These species use behavioral adaptations and nocturnal hypothermia, which reduce energetic costs. These adjustments could reduce the need for extensive metabolic adjustments typically found in small passerines that overwinter in cold regions. In addition, these species live at higher altitudes, which may also decrease metabolic acclimatization found in birds. Winter birds tolerated colder test temperatures than summer birds. This improved cold tolerance was associated with an increase in maximal thermogenic capacity or summit metabolism (M sum ). Winter M sum exceeded summer M sum by 26.1% in chickadees and 16.2% in titmice. Basal metabolic rates (BMR) were also significantly higher in winter birds compared with summer birds. Pectoralis wet muscle mass increased 33.3% in chickadees and 24.1% in titmice in winter and paralleled the increased M sum and BMR. Dry mass of contour plumage increased in winter for both species and was associated with decreased thermal conductance in winter chickadees compared to summer chickadees. Chickadees and titmice show metabolic acclimatization similar to other temperate species.

In endotherms, metabolic performance is associated with a wide array of ecological traits, including species distribution. Researchers have suggested that the northern boundaries of North American passerines are limited by their ability to sustain the high metabolic rates required for thermoregulation. Black-capped chickadees (Poecile atricapillus; BC) are year-round residents in most of Canada and the northern half of the United States, whereas Carolina chickadees (Poecile carolinensis; CA) are found exclusively in the southeastern United States. These species hybridize along a narrow contact zone that has been moving northward at a rate of about 1.6 km per decade, coincident with warming temperatures in Ohio. The location of the chickadee hybrid zone in Ohio closely matches air temperature isotherms, further suggesting that metabolic rate may correlate with distribution in these species. We tested the hypothesis that distribution patterns of chickadees are linked with their rate of metabolism. For populations of BC and CA chickadees, we measured basal metabolic rates (BMRs) and cold-induced peak metabolic rates from areas that differ in winter temperatures and supplemented this information with data from other studies. Although our findings suggest a general relationship between lower air temperatures and higher metabolic rate among black-capped chickadee populations, this trend was not robust across all locations. There was no significant relationship between lower air temperatures and metabolism in Carolina chickadees. Within Ohio, hybrids had a significantly higher mass-corrected BMR than either parental species. We suggest that the mtDNA-nDNA mismatch of hybrids may produce less efficient mitochondrial protein complexes, which in turn affects the efficiency of ATP production, thereby increasing rate of oxygen consumption to meet ATP demands.

Passerines that overwinter in temperate climates undergo seasonal acclimatization that is characterized by metabolic adjustments that may include increased basal metabolic rate (BMR) and cold-induced summit metabolism (M(sum)) in winter relative to summer. Metabolic changes must be supported by equivalent changes in oxygen transport. While much is known about the morphology of the avian respiratory system, little is known about respiratory function under extreme cold stress. We examined seasonal variation in BMR, M(sum), and ventilation in seasonally acclimatized house sparrows from Wisconsin. BMR and M(sum) increased significantly in winter compared with summer. In winter, BMR increased 64%, and M(sum) increased 29% over summer values. The 64% increase in winter BMR is the highest recorded for birds. Metabolic expansibility (M(sum)/BMR) was 9.0 in summer and 6.9 in winter birds. The metabolic expansibility of 9.0 in summer is the highest yet recorded for birds. Ventilatory accommodation under helox cold stress was due to changes in breathing frequency (f), tidal volume, and oxygen extraction efficiency in both seasons. However, the only significant difference between summer and winter ventilation measures in helox cold stress was f. Mean f in helox cold stress for winter birds was 1.23 times summer values.

The underlying assumption of the aerobic capacity model for the evolution of endothermy is that basal (BMR) and maximal aerobic metabolic rates are phenotypically linked. However, because BMR is largely a function of central organs whereas maximal metabolic output is largely a function of skeletal muscles, the mechanistic underpinnings for their linkage are not obvious. Interspecific studies in birds generally support a phenotypic correlation between BMR and maximal metabolic output. If the aerobic capacity model is valid, these phenotypic correlations should also extend to intraspecific comparisons. We measured BMR, M sum (maximum thermoregulatory metabolic rate) and MMR (maximum exercise metabolic rate in a hop-flutter chamber) in winter for dark-eyed juncos ( Junco hyemalis ), American goldfinches ( Carduelis tristis; M sum and MMR only), and black-capped chickadees ( Poecile atricapillus ; BMR and M sum only) and examined correlations among these variables. We also measured BMR and M sum in individual house sparrows ( Passer domesticus ) in both summer, winter and spring. For both raw metabolic rates and residuals from allometric regressions, BMR was not significantly correlated with either M sum or MMR in juncos. Moreover, no significant correlation between M sum and MMR or their mass-independent residuals occurred for juncos or goldfinches. Raw BMR and M sum were significantly positively correlated for black-capped chickadees and house sparrows, but mass-independent residuals of BMR and M sum were not. These data suggest that central organ and exercise organ metabolic levels are not inextricably linked and that muscular capacities for exercise and shivering do not necessarily vary in tandem in individual birds. Why intraspecific and interspecific avian studies show differing results and the significance of these differences to the aerobic capacity model are unknown, and resolution of these questions will require additional studies of potential mechanistic links between minimal and maximal metabolic output.