Seasonal changes in the thermoenergetics of the marsupial sugar glider, Petaurus breviceps

Little information is available on seasonal changes in thermal physiology and energy expenditure in marsupials. To provide new information on the subject, we quantified how body mass, body composition, metabolic rate, maximum heat production, body temperature and thermal conductance change with season in sugar gliders (Petaurus breviceps) held in outdoor aviaries. Sugar gliders increased body mass in autumn to a peak in May/June, which was caused to a large extent by an increase in body fat content. Body mass then declined to minimum values in August/September. Resting metabolic rate both below and above the thermoneutral zone (TNZ) was higher in summer than in winter and the lower critical temperature of the TNZ occurred at a higher ambient temperature (Ta) in summer. The basal metabolic rate was as much as 45% below that predicted from allometric equations for placental mammals and was about 15% lower in winter than in summer. In contrast, maximum heat production was raised significantly by about 20% in winter. This, together with an approximately 20% decrease in thermal conductance, resulted in a 13 degrees C reduction of the minimum effective Ta gliders were able to withstand. Our study provides the first evidence that, despite the apparent lack of functional brown adipose tissue, sugar gliders are able to significantly increase heat production in winter. Moreover, the lower thermoregulatory heat production at most TaS in winter, when food in the wild is scarce, should allow them to reduce energy expenditure.     

Seasonal variations in basal metabolic rate, lower critical temperature and responses to temporary starvation in the arctic fox (Alopex lagopus) from Svalbard

Metabolic rates of four resting, post-absorptive male adult summer- and winter-adapted captive arctic foxes (Alopex lagopus) were recorded. Basal metabolic rates (BMR) varied seasonally with a 36% increase from winter to summer, while body mass was reduced by 17% in the same period. The lower critical temperature (T _1c) of the winter-adapted arctic fox was estimated to −7°C, whereas T _lc during summer was 5°C. The similarity of these values, which are much higher than hitherto assumed (e.g. Scholander et al. 1950b), is mainly due to a significantly (P<0.05) lower BMR in winter than in summer. Body core (stomach) temperature was stable, even at ambient temperatures as low as −45°C, but showed a significant (P<0.05) seasonal variation, being lower in winter (39.3±0.33°C) than in summer (39.8±0.16°C). The thermal conductivity of arctic fox fur was the same during both seasons, whereas the thermal conductance in winter was lower than in summer. This was reflected in an increase in fur thickness of 140% from summer to winter, and in a reduced metabolic response to ambient temperatures below T _lc in winter. Another four arctic foxes were exposed to three periods of forced starvation, each lasting 8 days during winter, when body mass is in decline. No significant reduction in mass specific BMR was observed during the exposure to starvation, and respiratory quotient was unchanged at 0.73±0.02 during the first 5 days, but dropped significantly (P<0.05) to 0.69±0.03 at day 7. Locomotor activity and body core (intraperitoneal) temperature was unaltered throughout the starvation period, but body mass was reduced by 18.5±2.1% during these periods. Upon re-feeding, locomotor activity was significantly (P<0.05) reduced for about 6 days. Energy intake was almost doubled, but stabilised at normal levels after 11 days. Body mass increased, but not to the level before the starvation episodes. Instead, body mass increased until it reached the reduced body mass of ad libitum fed control animals. This indicates that body mass in the arctic fox is regulated according to a seasonally changing set point.     

Daily rhythm of oxygen consumption and thermoregulatory responses in some European winter- or summer-acclimatized finches at different ambient temperatures

The oxygen consumption of European finches, the siskin (Carduelis spinus), the brambling (Fringilla montifringilla), the bullfinch (Pyrhulla pyrhulla), the greenfinch (Carduelis chloris) and the hawfinch (Coccothraustes coccothraustes), was recorded continuously while ambient temperature was decreased stepwise from +30 down to-75°C. The oxygen consumption, body temperature (telemetrically), and shivering (integrated pectoral electromyography) of greenfinches were measured simultaneously at ambient temperatures between +30 and-75°C. Maximum heat production, cold limit, lower critical temperature, basal metabolic rate and thermal conductance (of the greenfinch) were determined. The diurnal variation of oxygen consumption of siskins and greenfinches was recorded at thermoneutrality and below the thermoneutral zone in winter- and summer-acclimatized birds. The diurnal variation of body temperature and thermal conductance of greenfinches were also determined. The diurnal variation of heat production was not seasonal or temperature dependent in the siskin and in the greenfinch. Nocturnal reduction of oxygen consumption saved 15–33% energy in the siskin and greenfinch. Body temperature of the greenfinch was lowered by 2.5–3.4°C. The nocturnal reduction of thermal conductance in the greenfinch was 39–48%. The basal metabolic rate was lowest in the largest bird (hawfinch) and highest in the smallest bird (siskin). The values were in the expected range. The heat production capacity of finches in winter was 4.7 times basal metabolic rate in the siskin, 4.2 times in the brambling, 3.5 times in the greenfinch and 2.9 times in the bullfinch and hawfinch. The heat production capacity of the siskin and greenfinch was not significantly lower in summer. The cold limit temperatures (°C) in winter were-61.2 in the siskin,-41.3 in the greenfinch,-37.0 in the bullfinch,-35.7 in the brambling and-28.9 in the hawfinch. The cold limit was 14.3°C higher in summer than in winter in the siskin and 8.7°C in the greenfinch. Thermal insulation of the greenfinch was significantly better in winter than in summer. The shivering of the greenfinch increased linearly when ambient temperature was decreased down to-40°C. Maintenance of shivering was coincident with season. In severe cold integrated pectoral electromyography did not correlate with oxygen consumption as expected. The possible existence of non-shivering thermogenesis in birds is discussed. It is concluded that the acclimatization of European finches is primarily metabolic and only secondly affected by insulation.Abbreviations AAT avian adipose tissue - bm body mass - BMR basal metabolic rate - C _t thermal conductance - EMG electromyogram - HP heat production - HP _max maximum heat production - MR metabolic rate - NST non-shivering thermogenesis - RMR resting metabolic rate - RQ respiratory quotient - T _a ambient temperature - T _b body temperature - T _c colonic temperature - T _1c lower critical temperature - TNZ thermoneutral zone - T _st shivering threshold temperature - V oxygen consumption     

Seasonal effects on thermoregulatory responses of the Rock Kestrel, Falco rupicolis

Thermoregulatory responses are known to differ seasonally in endotherms and this is often dependent on the environment and region they are resident. Holarctic animals are exposed to severe winters and substantial seasonal variation in ambient temperature. In contrast, those in the Afrotropics have less severe winters, but greater variation in temperature, rainfall and net primary production. These environmental factors place different selection pressures on physiological responses in endotherms. In this study, metabolic rate (VO₂) and body temperature (T_b) were measured in captive bred Rock Kestrels (Falco rupicolus) from the Afrotropics after a period of summer and winter acclimatisation. Resting metabolic rate was significantly lower after the winter acclimatisation period than after the summer acclimatisation period, and there was a shift in the thermoneutral zone from 20–33 °C in summer to 15–30 °C in winter. However, no significant difference in basal metabolic rate between summer and winter was found. The results show that Rock Kestrels reduce energy expenditure at low ambient temperatures in winter as expected in an Afrotropical species.     

Do season and distribution affect thermal energetics of a hibernating bat endemic to the tropics and subtropics?

Although many tropical and subtropical areas experience pronounced seasonal changes in weather and food availability, few studies have examined and none have compared the thermal physiology and energetics of a hibernating mammal that is restricted to these regions. We quantified thermal energetics of northern long-eared bats (Nyctophilus bifax; body mass ～10 g) during summer, winter, and spring from a subtropical habitat, and also during winter from a tropical habitat, to determine how N. bifax cope with climate and seasonal changes in weather. We captured bats in the wild and measured metabolic rates via open-flow respirometry. The basal metabolic rate of subtropical bats at an ambient temperature (T(a)) of 32.6 ± 0.7°C was 1.28 ± 0.06 ml O(2)·g(-1)·h(-1) during both summer and winter, similar to other species of Nyctophilus. Resting metabolic rates below the thermoneutral zone increased similarly with decreasing T(a) during all seasons and in both regions. All individuals showed a high proclivity to enter torpor at T(a) values below the thermoneutral zone. Metabolic rates in torpid thermoconforming bats fell with T(a) and body temperature, and mean minimum metabolic rates during torpor were similar during all seasons and in both regions and as predicted from body mass in temperate zone hibernators. At very low T(a), torpid N. bifax thermoregulated, and this threshold T(a) differed significantly between subtropical (T(a) = 3.5 ± 0.3°C) and tropical (T(a) = 6.7 ± 0.7°C) individuals, but not between seasons. Our data show that thermal energetics of N. bifax do not vary seasonally and in many aspects are similar in tropical and subtropical bats; however, torpid individuals from the subtropics allow body temperature to fall to significantly lower values than those from the tropics.     

Seasonal variations in the behavioural thermoregulation of roosting Humboldt penguins ( Spheniscus humboldti) in north-central Chile

We examined the thermoregulatory behaviour (TRB) of roosting Humboldt penguins (Spheniscus humboldti) in north central Chile during summer and winter, when ambient temperatures (T_a) are most extreme. Each body posture was considered to represent a particular TRB, which was ranked in a sequence that reflected different degrees of thermal load and was assigned an arbitrary thermoregulatory score. During summer, birds exhibited eight different TRBs, mainly oriented to heat dissipation, and experienced a wide range of T_a (from 14 to 31°C), occasionally above their thermoneutral zone (TNZ, from 2 to 30°C), this being evident by observations of extreme thermoregulatory responses such as panting. In winter, birds exhibited only three TRBs, mainly oriented to heat retention, and experienced a smaller range of T_a (from 11 to 18°C), always within the TNZ, even at night. The components of behavioural responses increased directly with the heat load which explains the broader behavioural repertoire observed in summer. Since penguins are primarily adapted in morphology and physiology to cope with low water temperatures, our results suggest that behavioural thermoregulation may be important in the maintenance of the thermal balance in Humboldt penguins while on land.     

Environmental profile and critical temperature effects on milk production of Holstein cows in desert climate

The environmental profile of central Arizona is quantitatively described using meteorological data between 1971 and 1986. Utilizing ambient temperature criteria of hours per day less than 21° C, between 21 and 27° C, and more than 27° C, the environmental profile of central Arizona consists of varying levels of thermoneutral and heat stress periods. Milk production data from two commercial dairy farms from March 1990 to February 1991 were used to evaluate the seasonal effects identified in the environmental profile. Overall, milk production is lower during heat stress compared to thermoneutral periods. During heat stress, the cool period of hours per day with temperature less than 21° C provides a margin of safety to reduce the effects of heat stress on decreased milk production. Using minimum, mean and maximum ambient temperatures, the upper critical temperatures for milk production are 21, 27 and 32° C, respectively. Using the temperature-humidity index as the thermal environment indicator, the critical values for minimum, mean and maximum THI are 64, 72 and 76, respectively.     

Torpor is not the only option: seasonal variations of the thermoneutral zone in a small primate

The reddish-gray mouse lemur (Microcebus griseorufus) is one of only a few small mammals inhabiting the spiny forest of southwestern Madagascar. In this study we investigated the physiological adjustments which allow these small primates to persist under the challenging climatic conditions of their habitat. To this end we measured energy expenditure (metabolic rate) and body temperature of 24 naturally acclimatized mouse lemurs, kept in outdoor enclosures, during different seasons (summer, winter, and the transition period between the two seasons). Mouse lemurs displayed two main physiological strategies to compensate seasonal and diurnal fluctuations of ambient temperature. On the one hand, individuals entered hypometabolism with decreasing ambient temperature (T _a) during the transition period and winter, enabling them to save up to 21 % energy per day (92 % per hour) compared with the normal resting metabolic rate at comparable T _a. On the other hand, euthermic mouse lemurs also showed physiological adjustments to seasonality when resting: the lower critical temperature of the thermoneutral zone decreased from summer to winter by 7.5 °C, which allowed mouse lemurs to keep energy demands constant despite colder T _as during winter. In addition, the basal metabolic rate was substantially lowered prior to the winter period, which facilitated accumulation of fat reserves. The combination of physiological modifications during euthermia in addition to hypometabolism, which can be individually adjusted according to external parameters and respective body condition, is important as it allows M. griseorufus to cope with the environmental variability of an energetically challenging habitat.     

Simple roost nests confer large energetic savings for sparrow-weavers

White-browed sparrow-weavers (Plocepasser mahali, body mass 40 g) are group-living passerines adapted to the semi-arid environment of north-eastern and south-western Africa. During winter, the nocturnal ambient temperature of these regions often falls below 0 degrees C. imposing conditions demanding an increase in thermoregulatory heat production. Individuals roost throughout the year in inverted U-shaped roost nests. We investigated the energetic advantages of roosting by measuring nest and ambient temperatures in the field, as well as the resting metabolic rate (RMR) of the birds. The sparrow-weavers exhibited a wide thermoneutral zone (13 degrees C - 32 degrees C). Although RMR at thermoneutrality (40.2 J g.h(-1)) conforms with those of other passerines. the value at 0 degrees C (74.8 J g.h(-1)) is significantly lower than expected. The slope of the line below the lower critical temperature is unexpectedly steep, however, and appears to cause the physiological requirement for nest roosting due to a high cost of thermoregulation at low temperatures, perhaps due to shivering or non-shivering thermogenesis. The nest temperature at 0 degrees C ambient is 5 degrees C. resulting in a saving of some 7% in the energy spent during winter nights when food resources are in short supply compared with the rest of the year.     

Body temperature null distributions in reptiles with nonzero heat capacity: seasonal thermoregulation in the American alligator (Alligator mississippiensis)

Regulation of body temperature may increase fitness of animals by ensuring that biochemical and physiological processes proceed at an optimal rate. The validity of current methods of testing whether or not thermoregulation in reptiles occurs is often limited to very small species that have near zero heat capacity. The aim of this study was to develop a method that allows estimation of body temperature null distributions of large reptiles and to investigate seasonal thermoregulation in the American alligator (Alligator mississippiensis). Continuous body temperature records of wild alligators were obtained from implanted dataloggers in winter (n=7, mass range: 1.6-53.6 kg) and summer (n=7, mass range: 1.9-54.5 kg). Body temperature null distributions were calculated by randomising behavioural postures, thereby randomly altering relative animal surface areas exposed to different avenues of heat transfer. Core body temperatures were predicted by calculations of transient heat transfer by conduction and blood flow. Alligator body temperatures follow regular oscillations during the day. Occasionally, body temperature steadied during the day to fall within a relatively narrow range. Rather than indicating shuttling thermoregulation, however, this pattern could be predicted from random movements. Average daily body temperature increases with body mass in winter but not in summer. Daily amplitudes of body temperature decrease with increasing body mass in summer but not in winter. These patterns result from differential exposure to heat transfer mechanisms at different seasons. In summer, alligators are significantly cooler than predictions for a randomly moving animal, and the reverse is the case in winter. Theoretical predictions show, however, that alligators can be warmer in winter if they maximised their sun exposure. We concluded that alligators may not rely exclusively on regulation of body temperature but that they may also acclimatise biochemically to seasonally changing environmental conditions.     

New national and regional bryophyte records, 32

Abstract

To fully hydrate patches of Crossidium crassinerve in the Mojave Desert, a rain event of at least 2.0 mm was required. When patches were hydrated for at least 3 days, mean daily ambient maximum/minimum temperatures were only 15.6/7.5°C. During the summer, patch temperatures exceeded ambient temperatures, whereas during the cooler months patch temperatures were lower than ambient temperatures, with degree of patch hydration not a factor in patch temperature. During patch hydration, mean surface patch temperature ranged from ?3 to 14°C. With few exceptions, patch hydroperiod (duration of patch hydration) was restricted to the cooler months spanning October to April, with the mean patch hydroperiod (among five patches) ranging from 3.7 to 4.9 days. While the most commonly recorded dry period was <25 days, Crossidium patches experienced longer periods of desiccation on nine occasions, with the longest period being 191 days. During a late winter rain event, patches dried slowly over a period of several days, whereas during a summer rain event, patches dried in as few as 3 h. Over the 4-year period, 248 sporophytes were initiated, with all but four of these from two patches. Only nine of these initiated sporophytes survived to disperse spores, with mortality attributed to embryonic abortion (69%) and capsule herbivory (30%).     

The importance of microhabitat in thermoregulation and thermal conductance in two namib rodents—a crevice dweller, Aethomys namaquensis, and a burrow dweller, Gerbillurus paeba

1. 1.|Thermoregulatory measurements of two Nambi rodents; Gerbillurus paeba, a burrow dweller, and Aethomys namaquensis, a crevice dweller were compared. Both were similar to other small arid-adapted rodents in that basal metabolic rates were reduced, thermoneutral zones narrow and evaporative water losses low. Rates of conductance and thermal lability, however, at ambient temperatures (T_a) below thermoneutral zone, were significantly different (P 0.01).

2. 2.|The rock rat A. namaquensis, living in a microclimate characterized by a large diel range and low humidities, compensates for a reduced basal metabolic rate by having a low rate of conductance. In this way it maintains precise thermoregulatory control. G. paeba, on the other hand, living in a thermally-stable milieu, does not control body temperature precisely. This animal instead utilizes a high rate of conductance to remove metabolic heat produced within the body. This would be advantageous to an animal living in a plugged burrow where the high humidities encountered impede the rate of evaporative cooling.

3. 3.|The energetic responses of both species, above the thermoneutral zone, appear to reflect very closely the environmental conditions which occur in the microhabitat that they rest in during the day. G. paeba shows less tolerance to temperature fluctuations than A. namaquensis, but shows more marked increases in short-term cooling mechanisms at high T_as.

4. 4.|Despite the increased use of evaporative cooling through salivation and panting in addition to pulmocutaneous evaporation, exposure to T_as above 38°C is rapidly lethal to G. paeba.

Thermal ecology of the mudskippers, Periophthalmus koelreuteri (Pallas) and Boleophthalmus boddarti (Pallas) of Kuwait Bay

The annual range of body temperatures (14–35°C) of emergent mudskippers are substantially less than that of air temperatures (10–42°C) as a result of behavioural thermoregulation. In winter, low surface temperatures are avoided by remaining in burrows. Newly emerged mudskippers then bask until body temperatures rise above 14°C before they move onto the mud. In summer, body temperatures are kept lower than ambient by selecting areas where evaporative cooling is high. Body temperatures generally match those of wet mud, which can be 7°C lower than air shade temperatures. The smaller, more terrestrial, Periophthalmus koelreuteri have body temperatures which are mainly lower in summer and higher in winter than Boleophthalmus boddarti .     

Seasonal thermoregulation in the burrowing parrot (Cyanoliseus patagonus)

Birds exposed to seasonal environments are faced with the problem of maintaining thermogenic homoeostasis. Previous studies have established that birds native to the Holarctic increase their Resting Metabolic Rate at different ambient temperatures (RMR_Ta) and Basal Metabolic Rate (BMR) in winter as an adaptation to cold temperature since winters are more severe, while their non-Holarctic counterparts generally decrease their winter BMR as an energy saving mechanism during unproductive and dry winter months. In this study, we examined seasonal thermoregulation in the burrowing parrot (Cyanoliseus patagonus), a colonial psittacine native to the Patagonian region of Argentina, a region with an unpredictable environment. We found significantly higher mass specific RMR_Ta and BMR in summer than in winter. Both summer and winter BMR of the species fell within the predicted 95% confident interval for a parrot of its size. Body mass was significantly higher in winter than in summer. The burrowing parrot had broad thermo-neutral zones in winter and summer. The circadian rhythm of core body temperature (T_b) of burrowing parrots was not affected by season, showing that this species regulated its T_b irrespective of season. These results suggest that the burrowing parrots' seasonal thermoregulatory responses represent that of energy conservation which is important in an unpredictable environment.     

Seasonal trends in body mass, food intake and resting metabolic rate, and induction of metabolic depression in arctic foxes (Alopex lagopus) at Svalbard

 Post-absorptive resting metabolic rates (RMRs), body mass and ad libitum food intake were recorded on an annual cycle in captive arctic foxes (Alopex lagopus) at Svalbard. During the light season in May and in the dark period in November, RMR during starvation and subsequent re-feeding were also measured. In contrast to earlier findings, the present study indicated a seasonal trend in post-absorptive RMR (in W · kg⁻¹ and W · kg^−0.75). The values in the light summer were 15% and 11% higher than the values in the dark winter, suggesting a physiological adaptation aiding energy conservation during winter in arctic foxes. Body mass and ad libitum food intake varied inversely through the year. A significant reduction in RMR (in W and W · kg^−0.75) with starvation (metabolic depression) was recorded both in May and November, indicating an adaptation to starvation in arctic foxes. The lack of metabolic depression during a period of starvation that was concomitant with extremely cold ambient temperatures in November 1994 indicates that metabolic responses to starvation may be masked by thermoregulatory needs. At very low ambient temperatures, arctic foxes may require increased heat production which cannot be achieved via below-average rates of metabolism. Accepted: 7 June 1999     

Metabolism and thermoregulation in the Cabrera vole (Rodentia: Microtus cabrerae)

Metabolism and thermoregulation were studied for the first time in the Cabrera vole (Microtus cabrerae), an endemic and threatened rodent of the Iberian Peninsula. Low values of resting metabolic rate (RMR) were registered (1.13 mlO(2) g(-1) h(-1)) at the lower limit of the thermoneutral zone (TNZ) (around 33.5 degrees C). Body temperature increased near the TNZ up to 37.3 degrees C but remained stable, around 36 degrees C, at ambient temperatures below 25 degrees C. Values of thermal conductance remained quite stable at ambient temperatures of 10-25 degrees C (0.144-0.160 mlO(2) g(-1) h(-1) degrees C) and increased to 0.301 mlO(2) g(-1) h(-1) degrees C at 33.5 degrees C. Data revealed that M. cabrerae developed a highly adaptive ability of conserving energy and lowering the metabolic cost of thermoregulation at high ambient temperatures, allowing the body temperature to approximate that of the environment and exhibiting low resting metabolic rate and high conductance.     

Redefining physiological responses of moose (Alces alces) to warm environmental conditions

We tested the concept that moose (Alces alces) begin to show signs of thermal stress at ambient air temperatures as low as 14 °C. We determined the response of Alaskan female moose to environmental conditions from May through September by measuring core body temperature, heart rate, respiration rate, rate of heat loss from exhaled air, skin temperature, and fecal and salivary glucocorticoids. Seasonal and daily patterns in moose body temperature did not passively follow the same patterns as environmental variables. We used large changes in body temperature (≥1.25 °C in 24hr) to indicate days of physiological tolerance to thermal stressors. Thermal tolerance correlated with high ambient air temperatures from the prior day and with seasonal peaks in solar radiation (June), ambient air temperature and vapor pressure (July). At midday (12:00hr), moose exhibited daily minima of body temperature, heart rate and skin temperature (difference between the ear artery and pinna) that coincided with daily maxima in respiration rate and the rate of heat lost through respiration. Salivary cortisol measured in moose during the morning was positively related to the change in air temperature during the hour prior to sample collection, while fecal glucocorticoid levels increased with increasing solar radiation during the prior day. Our results suggest that free-ranging moose do not have a static threshold of ambient air temperature at which they become heat stressed during the warm season. In early summer, body temperature of moose is influenced by the interaction of ambient temperature during the prior day with the seasonal peak of solar radiation. In late summer, moose body temperature is influenced by the interaction between ambient temperature and vapor pressure. Thermal tolerance of moose depends on the intensity and duration of daily weather parameters and the ability of the animal to use physiological and behavioral responses to dissipate heat loads.     

The roles of energetics,water economy,foraging behavior,and geothermal refugia in the distribution of the bat,Macrotus californicus

Summary Energy metabolism, thermoregulation, and water flux ofMacrotus californicus, the most northerly representative of the Phyllostomidae, were studied in the laboratory using standard methods, and energy metabolism and water fluxes were studied in the field using the doubly labelled water method together with a time budget. Daily energy expenditures of free-living bats averaged 22.8 kJ during the winter study period. Approximately 60% of this was allocated to resting metabolism costs while in the primary roosts (22 h/day).Macrotus californicus is unable to use torpor. The thermoneutral zone (TNZ) in this species is narrow (33 to 40 °C) and metabolic rate increased rapidly as ambient temperature decreased below the TNZ. Basal metabolic rate was 1.25 ml O₂/g·h, or 24 J/g·h. Total thermal conductance below the TNZ. was 1.8 mW/g·°C, similar to values measured for other bats. Evaporative water loss showed a hyperbolic increase with increasing ambient temperature, and was approximately 1% of total body mass/h in the TNZ. The success of these bats as year-round residents in deserts in the southwestern United States is probably not due to special physiological adaptations, but to roosting and foraging behavior. They use geothermally-heated winter roost sites (stable year-round temperatures of approximately 29 °C) which minimize energy expenditures, and they have an energetically frugal pattern of foraging that relies on visual prey location. These seem to be the two major factors which have allowedM. californicus to invade the temperate zone.Abbreviations BMR basal metabolic rate - FMR field metabolic rate - T _a ambient temperature - T _b body temperature - T _lc,T _uc lower and upper critical temperature, respectively - TBW total body water - TNZ thermoneutral zone     

Parallel evolution of thermophilia: daily and seasonal foraging patterns of heat‐adapted desert ants: Cataglyphis and Ocymyrmex species*

In the deserts of northern and southern Africa, respectively, ants of the genera Cataglyphisf oerster (Formicinae) and Ocymyrmexe mery (Myrmicinae) occupy the same ecological niche, which comprises that of a strictly diurnal thermophilic scavenger. Their daily foraging activities exhibit a bimodal pattern in summer and unimodality or complete inactivity in winter. The present study investigates whether these overall patterns are a result of endogenous annual activity rhythms of the colony or are triggered directly by the prevailing ambient temperatures. By exploiting various seasonal temperature regimes and, in particular, by creating near‐nest winter conditions experimentally in summer, it is shown that the latter hypothesis is generally true. However, there are daily and annual variations in the temperature set points at which foraging activities start and finish. These temperatures are lower in the winter than in the summer months and, in summer, they are lower in the morning than in the afternoon. The level of foraging activity in the afternoon reaches maximum values at surface temperatures of 60–63 °C. This means that, in summer months, these thermophilic ants concentrate their foraging activities into a period of almost lethal temperature regimes, during which they have to devote a substantial portion of their time outside the nest to respite (i.e. cooling‐off) behaviour.     

The physiology of hypothermia in the black-capped Chickadee,Parus atricapillus

Summary The shivering, body temperature, and metabolic response to stable and decreasing ambient temperature were measured in winter acclimatized Black-capped Chickadees,Parus atricapillus. Shivering activity, measured by duration and amplitude of bursts, increased curvilinearly from thermoneutral temperatures of 27°C down to 0°C. This parabolic shivering response may be a major component of the curvilinear response of metabolism to decreasing ambient temperature.Birds exposed to 0°C exhibited metabolism 32–45% lower than predicted for a 12-g homeotherm and body temperatures 10°C below the pre-experimental nocturnal body temperature. This hypothermia was not the result of a breakdown in thermoregulation, but was a controlled effort serving to reduce overnight energy expenditure. It is suggested that (1) hypothermia was achieved by decreased shivering by pectoral muscles during exposure to decreasing ambient temperatures, (2) the rate of body temperature decline was moderated by intermittent and reduced bursts during the cooling period, and (3) body temperature was maintained at a particular level during exposure to a stable low ambient temperature by intense bursts lasting one to three minutes.The physiology of hypothermia in chickadees is similar to torpor; however, chickadees did not arouse to a normal diurnal body temperature in the laboratory, and their hypothermia was not induced by inanition or prolonged exposure to cold, as reported for other species capable of torpor.