Black bears hibernate for 5 to 7 months a year and, during this time, do not eat, drink, urinate, or defecate. We measured metabolic rate and body temperature in hibernating black bears and found that they suppress metabolism to 25% of basal rates while regulating body temperature from 30° to 36°C, in multiday cycles. Heart rates were reduced from 55 to as few as 9 beats per minute, with profound sinus arrhythmia. After returning to normal body temperature and emerging from dens, bears maintained a reduced metabolic rate for up to 3 weeks. The pronounced reduction and delayed recovery of metabolic rate in hibernating bears suggest that the majority of metabolic suppression during hibernation is independent of lowered body temperature.

Muskoxen (Ovibos moschatus) are an integral component of Arctic biodiversity. Given low genetic diversity, their ability to respond to future and rapid Arctic change is unknown, although paleontological history demonstrates adaptability within limits. We discuss status and limitations of current monitoring, and summarize circumpolar status and recent variations, delineating all 55 endemic or translocated populations. Acknowledging uncertainties, global abundance is ca 170 000 muskoxen. Not all populations are thriving. Six populations are in decline, and as recently as the turn of the century, one of these was the largest population in the world, equaling ca 41% of today's total abundance. Climate, diseases, and anthropogenic changes are likely the principal drivers of muskox population change and result in multiple stressors that vary temporally and spatially. Impacts to muskoxen are precipitated by habitat loss/degradation, altered vegetation and species associations, pollution, and harvest. Which elements are relevant for a specific population will vary, as will their cumulative interactions. Our summaries highlight the importance of harmonizing existing data, intensifying long-term monitoring efforts including demographics and health assessments, standardizing and implementing monitoring protocols, and increasing stakeholder engagement/contributions.

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The microanatomy of healthy beaks and claws in passerine birds has not been well described in the literature, despite the importance of these structures in avian life. Histological processing of hard-cornified tissues is notoriously challenging and only a few reports on effective techniques have been published. An emerging epizootic of beak deformities among wild birds in Alaska and the Pacific Northwest region of North America recently highlighted the need for additional baseline information about avian hard-cornified structures. In this study, we examine the beak and claw of the Black-capped Chickadee (Poecile atricapillus), a common North American passerine that is affected by what has been described as "avian keratin disorder." We use light and scanning electron microscopy and high-magnification radiography to document the healthy microanatomy of these tissues and identify features of functional importance. We also describe detailed methods for histological processing of avian hard-cornified structures and discuss the utility of special stains. Results from this study will assist in future research on the functional anatomy and pathology of hard-cornified structures and will provide a necessary reference for ongoing investigations of avian keratin disorder in Black-capped Chickadees and other wild passerine species.

Black bears overwintering in outdoor hibernacula in Alaska decrease metabolism to as low as 25 % basal rates, while core body temperature (T(b)) decreases from 37 to 38 °C to a mid-hibernation average of 33 °C. T b develops cycles of 1.6-7.3 days length within a 30-36 °C range, with no circadian component. We do not know the mechanism or function underlying behind the T(b) cycles, although bears avoid T(b) of <30 °C and shorter cycles are predicted from higher rates of heat loss in colder conditions. To test this we manipulated den temperatures (T(den)) of 12 hibernating bears with body mass (BM) from 35.5 to 116.5 kg while recording T(b), metabolic rate (M), and shivering. T b cycle length (0.8-11.2 days) shortened as T den decreased (partial R(2) = 0.490, p < 0.001). Large bears with low thermal conductance (TC) showed more variation in T b cycle length with changes in T(den) than did smaller bears with high TC. Minimum T b across cycles was not consistent. At low T(den) bears shivered both during rising and decreasing phases of T(b) cycles, with minimum shivering during the fastest drop in T(b). At higher T den the T b pattern was more irregular. Mean M through T(b) cycles was negatively correlated to T den below lower critical temperatures (1.4-10.4 °C). Minimum M (0.3509 W/kg ± 0.0121 SE) during mid-hibernation scaled to BM [M (W) = 1.217 × BM (kg)(0.6979), R(2) = 0.855, p < 0.001]. Hibernating thermal conductance (TC) was negatively correlated to BM (R(2) = 0.721, p < 0.001); bears with high TC had the same T(b) cycle length as bears with low TC except at high T(den), thus not supporting the hypothesis that cooling rate alone determines T(b) cycle length. We conclude that T(b) cycling is effected by control of thermoregulatory heat production, and T(b) cycling may not be present when hibernating bears use passive thermoregulation. More intense shivering in the rising phase of cycles may contribute to the prevention of muscle disuse atrophy. Bears hibernating in cold conditions use more energy during hibernation than in warmer conditions. At T den below lower critical temperature, no extra energy expenditure results from T b cycling compared to keeping a stable T(b.)