Seasonal use of torpor by free-ranging Australian owlet-nightjars (Aegotheles cristatus)

With the exception of some data for common poorwills (Phalaenoptilus nuttallii) and anecdotal reports for a few other species, knowledge about the use of torpor by free-ranging birds is limited. Our study was designed to assess the use of torpor by free-ranging Australian owlet-nightjars (Aegotheles cristatus). We selected this species for study because of their relatively small body size (50 g), arthropod diet, nocturnal sedentary nature, taxonomic affiliation with other birds for whom the use of torpor is well documented, use of cavity roosts, and because of the cold winter (mean July minimum ambient temperature [T(a)] of approximately 0 degrees C) in the study area. We tracked 12 owlet-nightjars carrying temperature-sensitive transmitters for a total of 906 bird-days (range of 15-115 d per individual). Five different individuals entered torpor on 96 d in total. Torpor bouts occurred only between May 8 and September 8, the coldest period of the year. The lowest skin temperature (T(skin)) recorded for any bird was 19.6 degrees C, and the lowest core temperature was 22.4 degrees C. Surprisingly, torpor was rarely used at night because birds usually foraged then. Instead, torpor typically began near dawn, even on cold nights. Torpor bouts beginning at dawn lasted approximately 4 h. On 36% of days when torpor was used at dawn, birds reentered torpor later in the day. Torpor was not used during the breeding season, but this period also corresponds to the warm part of the year. There were no distinct daily minimum, maximum, or mean T(a) thresholds that could be used to reliably distinguish days when dawn torpor was used from those when it was not, although torpor was commonly employed when daily minimum T(a) fell below 3.9 degrees C. Our results show that even though Australia is typically thought of as a warm continent, at least some of the avifauna use torpor as a regular means of saving energy. We hypothesise that the reasons for this species' use of torpor include its ability to remain active all night foraging, either for terrestrial arthropods while walking or for flying insects taken on the wing, and/or its habit of roosting in cavities, which allows them to remain hidden in the daytime.     

光照黑暗循环条件下达乌尔黄鼠的冬眠模式和能量消耗

为研究冬眠季节的光照条件对贮脂类冬眠动物入眠的影响,在达乌尔黄鼠腹腔埋植体温记录元件iButton,在体重高峰后的下降阶段置于5℃和12L:12D的光照条件下,观察测定其冬眠模式和能量消耗。达乌尔黄鼠冬眠模式出现深冬眠型、少冬眠型和不冬眠型,蛰眠阵包括深冬眠阵、短冬眠阵和日眠阵。不同冬眠阵中最低体温、冬眠阵的持续时间、阵间产热的持续时间、冷却速率和复温速率差异显著;阵间产热的最高体温基本相同。平均每日能量消耗在日眠阵中最高、短冬眠阵中居中、深冬眠阵中最低。入眠时间多集中于黑暗时相,觉醒时间多集中于光照时相。本实验结果提示,在冬眠季节施加光照黑暗循环条件可减少达乌尔黄鼠冬眠的时间,升高阵间最低体温,缩短冬眠阵与阵间产热的持续时间,降低复温速率;增加冬眠期间能量消耗。入眠与觉醒受光照条件影响,具有明显的光暗节律。     

Exogenous passive heating during torpor arousal in free-ranging rock elephant shrews, <Emphasis Type="Italic">Elephantulus myurus</Emphasis>

In the laboratory rock elephant shrews (Elephantulus myurus; mean body mass 56.6 g) displayed the lowest torpor T_{b min} yet recorded (ca. 5°C) in a placental daily heterotherm. It was unknown whether these low T_bs were characteristic of daily heterothermy in free-ranging animals. It was also unclear how cost effective these low T_bs were since considerable energy is required to arouse from low T_bs on a daily basis. We continuously measured body temperature once every hour for 85 days in 13 free-ranging E. myurus from May to August 2001 (winter) in Weenen Game Reserve, KwaZulu-Natal, South Africa. We recorded a total of 412 torpor bouts. Free-ranging E. myurus had a high propensity for torpor with females displaying higher torpor frequency than males. The lowest T_b recorded was 7.5°C at T_a=2.7°C and the minimum torpor T_b was strongly correlated with ambient temperature. Torpor arousal was tightly coupled with ambient temperature cycles. Low torpor T_{b min} at low T_as was therefore cost-effective because the animals offset the high cost of arousal through exogenous passive heating. Laboratory studies under constant ambient temperatures may therefore underestimate the energetic benefits of torpor in free-ranging small mammals that inhabit regions where seasonality is moderate.     

Summer and winter torpor use by a free-ranging marsupial

Torpor is usually associated with low ambient temperatures (T(a)) in winter, but in some species it is also used in summer, often in response to limited food availability. Since the seasonal expression of torpor of both placental and marsupial hibernators in the wild is poorly documented by quantitative data, we investigated torpor and activity patterns of the eastern pygmy-possum Cercartetus nanus (17.4 g) over two seasons. We used radio telemetry to track animals during winter (n=4) and summer (n=5) in a warm-temperate habitat and found that torpor was used in both seasons. In winter all animals entered periods of short-term hibernation (from 5 to 20 days) containing individual torpor bouts of up to 5.9 days. In summer, torpor bouts were always <1 day in duration, only used by males and were not related to daily mean T(a). Pygmy-possums entered torpor at night as T(a) cooled, and rewarmed during the afternoon as T(a) increased. Individuals interspersed torpor bouts with nocturnal activity and the percentage of the night animals were active was the same in summer and winter. Our study provides the first information on torpor patterns in free-ranging C. nanus, and shows that the use of torpor throughout the year is important for energy management in this species.     

Confirmation of pleisiomorphic daily torpor in mammals: the round-eared elephant shrew Macroscelides proboscideus (Macroscelidea)

The characteristics of daily torpor were measured in the round-eared elephant shrew Macroscelides proboscideus (Macroscelidea) in response to ambient temperature and food deprivation. Elephant shrews are an ancient mammal order within a superordinal African clade including hyraxes, elephants, dugongs and the aardvark. M. proboscideus only employed torpor when deprived of food; torpor did not occur under an ad libitum diet at ambient temperatures of 10, 15 and 25?°C. Torpor bout duration ranged from <1?h to ca. 18?h. The times of entry into torpor were restricted to the scotophase, despite normothermic body temperature patterns indicating a rest phase coincident with the photophase. Full arousal was always achieved within the first 3?h of the photophase. When food deprived, the onset of the rest phase, and hence torpor, advanced with respect to the experimental photoperiod. The lowest torpor body temperature measured was 9.41?°C. Daily torpor in M. proboscideus confirms a pleisiomorphic origin of daily heterothermy. Torpor facilitates risk-averse foraging behaviour in these small omnivores by overcoming long-term energy shortfalls generated by the inherent variability of food availability in their semi-arid, El Niño-afflicted habitats.     

Torpor and activity patterns in free-ranging sugar gliders Petaurus breviceps (Marsupialia)

Almost all studies on daily torpor in mammals have been conducted in the laboratory under constant environmental conditions. We investigated torpor and activity patterns in free-ranging sugar gliders (Petaurus breviceps, 100 g) using temperature telemetry and compared field data with published information obtained in the laboratory. Body and/or skin temperature and activity patterns of 12 sugar gliders were monitored from autumn to spring. Healthy sugar gliders were active between sunset and sunrise, but on cold or rainy nights activity was substantially reduced. Animals in poor condition occasionally foraged during the day. Eleven gliders were monitored for 8–171 days and all of these entered daily torpor. Torpor was observed on 103 days (17% of observation days), usually occurred on rainy or cold nights, and frequency of torpor changed with season. Torpor bouts lasted between 2 and 23 h (average 13 h) and the body temperature fell to a minimum of 10.4°C. Torpor was thus much deeper, longer and more frequent than in laboratory studies on the same species. Our study shows that cold or wet conditions curtail foraging in wild sugar gliders and that they employ daily torpor regularly during adverse weather. This suggests that minimisation of energy loss by the use of torpor in sugar gliders is pivotal for their survival in the wild. Received: 8 July 1999 / Accepted: 23 December 1999     

Energetic consequences and ecological significance of heterothermy and social thermoregulation in striped skunks (Mephitis mephitis)

We assessed patterns and energetic consequences of different overwintering strategies, torpor, and social thermoregulation in the striped skunk (Mephitis mephitis) under natural ambient temperature and photoperiod. Striped skunks entered spontaneous daily torpor, with the lowest torpid body temperature (T(b)) reaching 26.0 degrees C, the lowest recorded T(b) for a carnivore. Patterns of daily torpor differed between solitary and grouped skunks: all solitary skunks regularly entered daily torpor, but only some individuals in communal dens employed torpor. When they did, it was shallow and infrequent. Solitary skunks entered torpor on average 50 times (in 120 d) compared with 6 times for grouped skunks. During torpor, solitary skunks had average minimum T(b) of 26.8 degrees C and bout duration of 7.8 h, whereas grouped skunks had average minimum T(b) of 30.9 degrees C and bout duration of 5.4 h. Torpor by solitary skunks occurred during their activity phase, but grouped skunks' shallow torpor bouts were restricted to their diurnal resting phase. On average, grouped skunks experienced lower percent daily fat loss, and they emerged in spring with higher percent body fat of 25.5%. In contrast, solitary skunks emerged in spring with only 9.3% body fat. In conclusion, the use of daily torpor and social thermoregulation in northern populations of striped skunks represent two strikingly different mechanisms to minimize energetic costs and increase individual fitness in response to unfavorable environmental conditions.     

Torpor in free-ranging tawny frogmouths (Podargus strigoides).

Several small caprimulgiform birds (<80 g) are known to enter torpor, apparently to cope with a fluctuating supply of insect prey. Since the large Australian tawny frogmouth (Podargus strigoides; 381-556 g) is also insectivorous, we investigated its thermoregulatory behaviour and thermal biology to determine whether this species is also heterothermic. In an open woodland at approximately 1,000 m altitude, we equipped eight free-ranging birds with external temperature-sensitive radio transmitters attached to an elastic harness to measure skin temperature (T(skin)). Core body temperature (T(b)) was measured in three of these birds fitted with an additional intraperitoneal transmitter. T(skin) was closely correlated with T(b), although T(skin) was usually several degrees below T(b). During the three coldest months of the year (June-August), shallow torpor with T(b) as low as 29.1 degrees C occurred frequently, whereas during spring and summer, torpor was not recorded. Torpor occurred either during the night and/or during the first half of the day. Night torpor bouts were initiated after a short activity period around dusk and lasted on average for about 7 h. Torpid birds always aroused before sunrise to either commence a second short foraging period or to fly directly to a day roost tree. After birds roosted, T(b) fell again around sunrise, and birds occasionally entered a second dawn torpor bout; however, in most cases, T(b) increased rapidly not long after entry, most likely due to passive heating by the sun. We conclude that despite their large body size and energetically conservative hunting strategy, tawny frogmouths, like several related caprimulgiform species, frequently enter shallow torpor when low T(a) demands high energetic costs for normothermic thermoregulation and likely reduces insect availability.     

Prey availability affects daily torpor by free-ranging Australian owlet-nightjars (Aegotheles cristatus)

Food availability, ambient temperatures (T(a)), and prevailing weather conditions have long been presumed to influence torpor use. To a large extent, this is based on measurements in the laboratory of animals placed on restricted diets and kept at low T (a). Information on the determinants of torpor employment in the field is limited. We assessed winter torpor by insectivorous, free-ranging Australian owlet-nightjars (Aegotheles cristatus; 22 birds, 834 bird-days over six winters). Birds in three habitats were investigated to test whether torpor use is affected by annual T(a), rainfall, and arthropod abundance. Owlet-nightjars entered daily torpor regularly at all sites. Torpor frequency, depth and bout duration were greatest during two periods with lower arthropod abundance, providing rare evidence of the link between food availability and torpor patterns of wild birds. Temporal organization of torpor was similar among sites, and nocturnal torpor was more frequent than previously reported. Our findings quantitatively demonstrate that reduced food resources affect torpor usage independently from T(a), and support the view that food availability is a primary ecological determinant of torpor use in the wild.     

The influence of environment,sex, and innate timing mechanisms on body temperature patterns of free-ranging black-tailed prairie dogs (Cynomys ludovicianus)

Mechanisms that influence body temperature patterns in black-tailed prairie dogs are not well understood. Previous research on both free-ranging and laboratory populations of black-tailed prairie dogs (Cynomys ludovicianus) has suggested that reductions in ambient temperature and food and water deprivation are the primary factors that stimulate torpor in this species. In other species, however, torpor has been shown to be influenced by a multitude of factors, including innate circadian and circannual timing mechanisms, energy status, and reproductive behaviors. Our objective was to clarify the influence of weather, sex, and intrinsic timing mechanisms on the body temperature patterns of free-ranging black-tailed prairie dogs. We monitored body temperatures of eight adult (>1 yr) prairie dogs from November 1999 to June 2000. Prairie dogs showed distinct daily and seasonal body temperature patterns, which reflected changes in ambient temperatures that occurred during these periods. These patterns of daily and seasonal heterothermy suggest that body temperature patterns of black-tailed prairie dogs may be driven by an innate timing mechanism. All prairie dogs entered torpor intermittently throughout winter and spring. Torpor bouts appeared to be influenced by precipitation and reductions in ambient temperature. Our results also suggest that reproductive behaviors and circadian timing may influence torpor in this species.     

Heterothermy in elephant shrews, Elephantulus spp. (Macroscelidea): daily torpor or hibernation?

The physiological parameters of heterothermy (e.g. minimum body temperature and oxygen consumption, percentage metabolic reduction, and bout length) were measured in two species of Elephantulus elephant shrews (Elephantulus myurus and Elephantulus rozeti; Macroscelidea) as a function of ambient temperature. Both species displayed deep torpor whereby the body temperatures of ca. 5 °C and oxygen consumption as low as 2% of basal metabolic rate were attained. Torpor bout length (n=57 bouts) never exceeded 24 h. These data are characteristic of both hibernation (minimum body temperature and metabolism) and daily torpor (bout length), and argue that these two physiological responses may not necessarily have separate evolutionary origins. Accepted: 26 July 2000     

Torpor characteristics and energy requirements of furless Siberian hamsters.

After approximately 10 wk of exposure to decreasing day lengths, Siberian hamsters (Phodopus sungorus) begin to display spontaneous torpor bouts several times each week. Torpor is associated with reduced daily energy expenditure and lower food consumption and ameliorates the thermoregulatory challenges of winter. We tested the extent to which the energy savings conferred by daily torpor depend on the presence of an insulative pelage. Female hamsters were housed in a winter day length (8L:16D) at 5 degrees C; daily food intake and torpor characteristics were recorded for 5 wk in shaved (furless) or normal hamsters. Torpor-bout incidence decreased by 62% in furless hamsters, but the duration of individual bouts and the minimum body temperature attained during torpor were unaffected by loss of pelage. Body temperature declined more rapidly during entry into torpor and increased more slowly during arousal from torpor in furless than in control hamsters. Energy savings per torpor bout, assessed by the amount of food consumed on days that included a torpor bout, was substantially greater in normal than in furless hamsters (16.0% vs. 3.3%); this difference likely reflects the increased cost of thermoregulation during torpor, as well as the increased caloric expenditure incurred by furless hamsters during arousal from torpor. An insulative pelage may be a prerequisite for the energetic benefits derived from heterothermy in this species.     

Body temperature patterns in two syntopic elephant shrew species during winter

We measured body temperature (T_b) in free-ranging individuals of two species of elephant shrews, namely western rock elephant shrews (Elephantulus rupestris) and Cape rock elephant shrews (E. edwardii), during winter in a winter-rainfall region of western South Africa. These syntopic species have similar ecologies and morphologies and thus potential for large overlaps in diet and habitat use. Unexpectedly, they displayed different T_b patterns. Western rock elephant shrews were heterothermic, with all individuals decreasing T_b below 30 °C on at least 34% of nights. The level of heterothermy expressed was similar to other species traditionally defined as daily heterotherms and was inversely related to T_a, as is commonly seen in small heterothermic endotherms. In contrast, Cape rock elephant shrews rarely allowed their T_b to decrease below 30 °C. The level of heterothermy was similar to species traditionally defined as homeotherms and there was no relationship between the level of heterothermy expressed and T_a. In both species, the minimum daily T_b was recorded almost exclusively at night, often shortly before sunrise, although in some individuals minimum T_b occasionally occurred during the day. The interspecific variation in T_b patterns among Elephantulus species recorded to date reiterates the importance of ecological determinants of heterothermy that interact with factors such as body mass and phylogeny.     

Natural use of heterothermy by a small, tree-roosting bat during summer

Little is known about the use of heterothermy by wild bats during summer, especially for tree-roosting species. Because thermal conditions within tree roosts can fluctuate widely with ambient temperature, which affects thermoregulatory energy expenditure during diurnal roosting, we measured skin temperatures of free-ranging male Nyctophilus geoffroyi (8 g) to quantify the relation between summer torpor use and roost thermal conditions. Bats roosted under bark on the northern (sunny) side of trees and entered torpor every day, usually near sunrise. Bats exhibited two bouts of torpor on most days: the first occurred in the morning, was terminated by partially passive rewarming, and was followed by a period of normothermy during the warmest part of the day; a second torpor bout occurred in the late afternoon, with arousal near sunset. On the warmest days, bats had only a single, short morning bout. On the coolest days, bats remained torpid throughout the day, and one 2-d bout was observed. Thus, presumably owing to their poorly insulated roosts and the high energetic cost of normothermy at temperatures below 30 degrees C, the extent and timing of heterothermy was closely related to the cycle of diurnal temperatures. Our study indicates that torpor use is important for energy maintenance during summer diurnal roosting of N. geoffroyi and likely of other small, tree-roosting bats.     

Summer torpor in a free-ranging bat from subtropical Australia

It is widely believed that torpor is mainly an adaptation of endotherms for cold stress and food limitation. We studied torpor use in the wild by a small tree-roosting microbat from a sub-tropical area during summer when food was abundant. Surprisingly, two torpor bouts per day were employed on each roost-day observed. The first bout occurred in the early morning and the second bout in the late afternoon, whilst a period of normothermia was maintained over the warmest part of the day. Torpor likely reduced energy expenditure substantially, and may be common in small microbats whose day-roosts are poorly insulated, even in sub-tropical climates.     

Thermal biology, torpor, and activity in free-living mulgaras in arid zone Australia during the winter reproductive season

Little is known about the energy conservation strategies of free-ranging marsupials living in resource-poor Australian deserts. We studied activity patterns and torpor of free-living mulgaras (Dasycercus blythi) in arid central Australia during the winter of 2006. Mulgaras are small (approximately 75 g), nocturnal, insectivorous marsupials, with a patchy distribution in hummock grasslands. Mulgaras (six males, three females) were implanted intraperitoneally with temperature-sensitive transmitters and monitored for 6-55 d. Temperature profiles for different microhabitats and the thermal properties of soil and a number of burrows were also measured. Air temperature ranged from -3 degrees C at night to 30 degrees C during the day. Although burrows buffered temperature extremes, the thermal diffusivity of the sandy soil was high, and many burrows were shallow. Hence, soil and burrow temperatures averaged about 15 degrees C. The activity of mulgaras was often restricted to a few hours after sunset, before they retired into their burrows. Mulgaras employed torpor frequently, often entering torpor during the night and arousing around midday, with arousals occurring later on cooler days. Shallow burrows allowed cooling below mean T(soil). Consequently, body temperatures as low as 10.8 degrees C were observed. The longest torpor bout was 20.8 h. Torpor patterns changed seasonally and differed between males and females. From June to August, females entered torpor almost daily despite mating and gestation, but from the end of the gestation period onward, they remained normothermic. In contrast, males showed only shallow and short torpor during the mating season, but from mid-July, a transition to more frequent and deeper torpor resembling that of females was observed. Apparently, in both sexes, the reproductive effort entails energetic costs, but torpor, as an energy-saving mechanism, and reproduction are not exclusive in mulgaras. In a resource-poor environment during the least productive part of the year, frequent torpor seems to provide the means to compensate for the increased energetic costs associated with reproduction.     

Hibernation by a free-ranging subtropical bat (Nyctophilus bifax)

Knowledge about torpor in free-ranging subtropical bats is scarce and it is widely believed that low and stable ambient temperatures are necessary for prolonged torpor. We present temperature-telemetry data from free-ranging male (n = 4) and female (n = 4) subtropical vespertilionid bats, Nyctophilus bifax (~10 g), exposed to pronounced daily fluctuations of ambient temperature. All bats used torpor on every day in winter and both males and females exhibited multi-day torpor bouts of up to 5.4 days. Although females were larger than males, patterns of torpor were similar in both sexes. Torpor use was correlated with prevailing weather conditions and, on days when bats remained torpid, maximum ambient temperature was significantly lower than on days when bats aroused. Moreover, the duration of interbout normothermic periods at night increased with increasing average nightly ambient temperature. Skin temperature of torpid bats varied by 10.2 ± 3.6°C day⁻¹ (n = 8, N = 47) and daily minimum skin temperature was positively correlated with the daily minimum ambient temperature. Our study shows that prolonged torpor is an important component of the winter ecology of a subtropical bat and that torpor and activity patterns of N. bifax predominantly reflect prevailing weather conditions.     

Some like it cold: summer torpor by freetail bats in the Australian arid zone

Bats are among the most successful groups of Australian arid-zone mammals and, therefore, must cope with pronounced seasonal fluctuations in ambient temperature (T _a), food availability and unpredictable weather patterns. As knowledge about the energy conserving strategies in desert bats is scant, we used temperature-telemetry to quantify the thermal physiology of tree-roosting inland freetail bats (Mormopterus species 3, 8.5 g, n = 8) at Sturt National Park over two summers (2010–2012), when T _a was high and insects were relatively abundant. Torpor use and activity were affected by T _a. Bats remained normothermic on the warmest days; they employed one “morning” torpor bout on most days and typically exhibited two torpor bouts on the coolest days. Overall, animals employed torpor on 67.9 % of bat-days and torpor bout duration ranged from 0.5 to 39.3 h. At any given T _a, torpor bouts were longer in Mormopterus than in bats from temperate and subtropical habitats. Furthermore, unlike bats from other climatic regions that used only partial passive rewarming, Mormopterus aroused from torpor using either almost entirely passive (68.9 % of all arousals) or active rewarming (31.1 %). We provide the first quantitative data on torpor in a free-ranging arid-zone molossid during summer. They demonstrate that this desert bat uses torpor extensively in summer and often rewarms passively from torpor to maximise energy and water conservation.     

Late-born intermittently fasted juvenile garden dormice use torpor to grow and fatten prior to hibernation: consequences for ageing processes

Torpor is thought to slow age-related processes and to sustain growth and fattening of young individuals. Energy allocation into these processes represents a challenge for juveniles, especially for those born late in the season. We tested the hypothesis that late-born juvenile garden dormice (Eliomys quercinus) fed ad libitum (‘AL’, n = 9) or intermittently fasted (‘IF’, n = 9) use short torpor bouts to enhance growth and fat accumulation to survive winter. IF juveniles displayed more frequent and longer torpor bouts, compared with AL individuals before hibernation. Torpor frequency correlated negatively with energy expenditure and water turnover. Hence, IF juveniles gained mass at the same rate, reached similar pre-hibernation fattening and displayed identical hibernating patterns and mass losses as AL animals. We found no group differences in relative telomere length (RTL), an indicator of ageing, during the period of highest summer mass gain, despite greater torpor use by IF juveniles. Percentage change in RTL was negatively associated with mean and total euthermic durations among all individuals during hibernation. We conclude that torpor use promotes fattening in late-born juvenile dormice prior to hibernation. Furthermore, we provided the first evidence for a functional link between time spent in euthermy and ageing processes over winter.     

Seasonal changes in daily torpor patterns of free-ranging female and male Daubenton’s bats (Myotis daubentonii)

Daily torpor can provide significant energy and water savings in bats during cold ambient temperatures and food scarcity. However, it may reduce rates of foetal and juvenile development. Therefore, reproductive females should optimize development by minimizing times in torpor. To test this hypothesis, the use of torpor by female and male free-ranging Daubenton’s bats (Myotis daubentonii) during reproduction (gestation, lactation, and post-lactation period) was investigated in 1998 and 1999. Temperature-sensitive radio transmitters were attached to the bats to measure skin temperature. Simultaneously, ambient temperature was recorded. While both sexes became torpid during daytime, male bats used daily torpor (>6°C below individual active temperature) significantly more often during reproductive period (mean: 78.4 % of day time in May and 43 % in June) than females. Female bats went into daily torpor, particularly in late summer when juveniles were weaned (mean: 66.6 % of daytime). Lowest skin temperatures occurred in a female bat with 21.0°C during post-lactation. Skin temperatures of male bats fluctuated from 16.8°C in torpor to 37.2°C during times of activity. There was a significant effect of reproductive period on skin temperature in females whereas mean ambient temperature had no significant effect. However, mean ambient temperature affected mean skin temperatures in males. Our findings indicate that female Daubenton’s bats adopt their thermoregulatory behaviour in particular to optimize the juvenile development.