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Flight rapidly modulates body temperature in freely behaving bats



Bats are remarkable in their dynamic control over body temperature, showing both hypothermia with torpor and hyperthermia during flight. Despite considerable research in understanding bats’ thermoregulation mechanisms, knowledge on the relationship between flight and body temperature in bats remains limited, possibly due to technological restraints.


We used onboard dataloggers including a temperature sensor and an inertial sensor (accelerometers) and continuously recorded the flight behavior and skin temperature (Tsk) subcutaneously of a perch-hunting bat, Hipposideros armiger, both in the laboratory and in the field. We provide evidence that flight increases the body temperature of bats. The median of the maximum increase in the Tsk caused by flight bouts was 3.4 °C (between 1.9 and 5.3 °C for different individuals) in the laboratory. The maximum Tsk for the bats was narrowly centered around 40 °C (between 38.5 and 40.9 °C). Moreover, we found that the faster the Tsk rises, the greater the maximum increase in Tsk. Interestingly, bats can slow down the Tsk rises with intermittent fights, during which they perch after brief flight bouts to allow the body temperature to drop rapidly. Similar data were collected from field recordings in free-ranging bats.


We suggest that perch-hunting behavior observed in approximately 200 species of bats that results in intermittent flights may function as a thermoregulatory strategy, in addition to optimizing energy efficiency as demonstrated by previous studies.


Bats are the second largest mammalian order and are widely distributed across the world [1]. Among several remarkable features of bats, dynamic control of body temperature over an extended range has attracted researchers’ attention for decades [2,3,4,5,6,7,8]. From a comparative perspective, several aspects of the body temperature in bats are of interest. First, bats can perform many typical activities in a much larger range of body temperatures than most mammals. For example, several species of bats can fly at a body temperature as low as 24 °C [9, 10], which is more than 10 °C below the homeothermic zone of 35–39 °C. Second, on a daily basis, many species of bats reduce their body temperature by many degrees based on the ambient environment to conserve energy, entering a special physiological status called torpor [5,6,7]. Some bats can also hibernate during the wintertime and their body temperature can be as low as a few degrees Celsius. Third, probably due to their unique ability of powered flight as a mammal, the body temperature of flying bats often surpasses the higher limit of their homeothermic zone [4, 9, 11]. Both hypothermia (torpor and hibernation) and hyperthermia (fever) are hypothesized to be related to the evolution of their exceptional immune system for defending ectoparasites and diseases [12,13,14], in addition to important physiological functions ranging from energy conservation to survival in hot conditions [4, 6, 15].

Over the years, several methods have been used to measure the body temperature of bats. Traditionally, fast-responding thermocouples were used to measure the rectal and skin temperatures for both hanging and flying bats [9, 16]. Thermocouples give instant temperatures and often require manual reading and noting. Thus, the body temperature of flying bats was all measured in a post-flight fashion after catching the bats [9, 10]. Miniature temperature sensors now allow continual body temperature monitoring and have been employed intensively for studying resting bats, particularly bats in hibernation or daily torpor [5, 17,18,19,20,21,22]. A few studies also applied thermal infrared imaging techniques to measure freely flying bats in the field [23,24,25]. These measurements allow detailed temperature comparisons between various body parts, but do not allow tracking an individual’s temperature over time, since they only allow measuring animals directly in front of the device. To date, there have been very few reports of continuous measurements of body temperature in flying bats [26].

In this study, we first conducted a literature review to evaluate the previous use of the available techniques for measuring body temperature in bats. Then, we present pilot data from synchronized measurements of the body temperature and flight behavior of free-flying great roundleaf bats (Hipposideros armiger) in the laboratory and in the wild, using onboard temperature and acceleration dataloggers (Fig. 1). The primary goal was to examine the potential of using onboard temperature sensors to quantify wild bat physiology and to provide new insight into the physiology of bats as they are flying in their natural environment. Early studies with thermocouples have shown that, shortly after flight onsets, the bat’s core body temperature rises [10, 16, 27]. Thus, we were keen to validate these findings in free-flying bats in the real world.

Fig. 1
figure 1

An illustration of the measurements of the body temperature and the flight behavior of a bat in the laboratory. A Z-acceleration can be used to identify the flight bouts of bats. When a bat starts to fly, the z-acceleration is characterized by a sudden increase in amplitude. When the bat stops flying, the z-acceleration amplitude returns to the baseline level. B The synchronized measurement of the Tsk surrounding the flight bouts as shown in A. C, D The zoom-in view and the spectrogram of the acceleration data for the section highlighted in red in A. The energy distribution of the spectrogram for the z-acceleration reflects the wingbeat frequency of the flying bat (which is centered around 6.8 Hz)


Research status of body temperature measurements in bats

Based on the online database Web of Science and our literature library, we identified a total of 179 studies reporting the body (skin) temperature of bats. Body temperature has been measured for 163 bat species from 14 families (Fig. 2A). Bats from the family Vespertilionidae are most intensively studied, representing 39% of the total, which was followed by the family Phyllostomidae and family Pteropodidae. Overall, there was an increase in the number of studies on the body temperature of bats over the years (Fig. 2B). In particular, the number of published studies during the past 30 years (1990–2020) represents 79% of the total studies. Methodologically, three measurement techniques were employed in studying bats’ body temperature: thermocouples, temperature sensors (temperature telemetry and onboard loggers), and thermal infrared-light imaging. Except for eight studies that used thermal infrared-light imaging techniques, all other studies either used thermocouples or temperature sensors. Before 1980, thermocouples were used for all, except one, of the 39 studies. Afterward, miniature temperature sensors were used more and more frequently. For the past two decades, 68 of 93 studies (73%) applied temperature sensors to measure the body temperature of bats. When studies were grouped by the study environment, it revealed that thermocouples were the dominant measurement device for studying bats’ body temperature in the laboratory, while temperature telemetry was the most popular technique for recording bats’ body temperature in the field (Fig. 2C). Regarding the behavioral context of the bats for the body temperature measurements, hanging bats and roosting bats were most commonly studied in the laboratory and the field, respectively (Fig. 2D). Notably, only four studies have recorded the body temperature of flying bats in the field and none of these studies collected flight data in parallel to the body temperature measurements as we did.

Fig. 2
figure 2

Research status on the body temperature of bats. A The proportion of the bat species from different families that the body temperature was measured. ‘Other families’ includes the families in which the number of species is less than six. B Counts of the studies on bat body temperature every decade since the year 1930, as well as the number of studies grouped by the measurement technique for each study. C Counts of the studies based on the measurement technique for both the laboratory and field studies. D Counts of the studies based on the behavior of the bats for both the laboratory and field studies. ‘Roosting’ behavior describes the studies that were carried out for bats at the roost and the bats can show both hanging and flying behavior, although the specific behavior of the bats during the recording was typically unknown. Seven of the studies used two measurement techniques and these studies were counted as two separate studies. Both the ‘Telemetry’ and ‘Onboard logger’ technique rely on miniature temperature sensors attached to the bat

Body temperature and flight behavior of H. armiger in the laboratory

We made synchronized and continuous recordings of the skin temperature (Tsk) and wingbeat behavior of 8 individual bats, using onboard temperature sensors and inertial sensors (accelerometers) in the laboratory. The temperature sensor was implanted subcutaneously, and thus measures an intermediate between the skin and the (core) body temperatures and is affected by ambient temperature to a lesser degree than external sensors (Additional file 1: Fig. S1). Example recordings of both the Tsk and the flight-induced acceleration from a bat are shown in Fig. 1A, B. Based on the change in the amplitude of the z-axis acceleration, flight bouts were identified (see “Methods”). The trace of the Tsk of individual bats is characterized by rapid changes during identified flight bouts (Fig. 1A, B). Across the 8 individuals of bats recorded, the medians of the minimum and maximum Tsk were 34.6 and 39.9 °C, respectively. The median Tsk was 36.0 °C. Both the median and the maximum Tsk were more similar across individuals, compared with the minimum Tsk (Fig. 3B). Specifically, the variation of the median and the maximum Tsk, as measured by the range, were 27% and 19% of the minimum Tsk, respectively (bootstrapping test, both P < 0.05).

Fig. 3
figure 3

Characteristics of the body temperature and the flight behavior for flying bats in the laboratory. A Continuous recording of the Tsk of two bats for the entire experimental session lasting for approximately two and a half hours. Time zero is the beginning time of the recording. B The minimum, median, and maximum Tsk of all eight bats recorded in the laboratory. Grey circles indicate the data of individual bats. C Counts of the wingbeat frequency of the bats based on accelerometer measurements with a bin size of 1 Hz. D Duration of the flight bouts in relation to the wingbeat frequencies. The sample size is indicated by the associated number

We used flight-induced acceleration changes to identify potential flight bouts and identified 55 flight bouts with a wingbeat frequency greater than 5 Hz (Fig. 3C). The flight bouts had a median wingbeat frequency of 7.2 Hz (Fig. 3C) and last on average 47.5 s (Fig. 3D). To quantify the effects of flight on the Tsk, we extracted the Tsk at the beginning of the flight bouts and the maximum Tsk. The time difference between these two temperature points was referred to as the rise time that consists of both the flight time and the short pauses between the flight bouts. As shown in the zoomed-in view of Fig. 4A, within the rise time window there are four identified flight bouts separated by short pauses during which no wingbeat was recorded. The temperature difference between these two temperature points was referred to as the maximum increase in Tsk (Fig. 4A). Additionally, we measured the decay time which was the required time for the maximum Tsk to drop to the level at the beginning of the flight onset (Fig. 4A). The median of the maximum increase in Tsk of individual bats was 3.4 °C, ranging from 1.9 to 5.3 °C (Fig. 4B). It took a median of 9 min for the bats to reach the maximum Tsk, while it took a median of 25 min for the Tsk to drop to the flight onset level (Fig. 4C). The rise time was significantly shorter than the decay time (Paired one-side t-test, t-stat = − 4, P = 0.005). Accordingly, the rate of Tsk change was more rapid for the rising phase than for the decaying phase of the Tsk (Fig. 4D; Paired one-side t-test, t-stat = 2.9, P = 0.018). Note, the decay time could not be estimated for two individuals because the Tsk of the bats remained high for the entire recording session.

Fig. 4
figure 4

Body temperature dynamics in flying bats in the laboratory. A Synchronized recordings of the skin temperature (Tsk) and flight behavior (as reflected by the Z-acceleration data). The rise time is measured as the time difference between the Tsk of the flight onset (left green circle) and the maximum Tsk (center green circle). The decay time is measured as the time difference between the maximum Tsk (center green circle) and the post-flight Tsk that equals to the Tsk at the flight onset (right green circle). The rise time and the decay time (i.e., a measurement of duration) consists of both the flight time and the short pauses between the flight bouts when no wingbeat was recorded. As shown in the zoomed-in view, there are four individual flight bouts separated by short pauses within the rise time window. Nevertheless, the decay time is largely dominated by the time when the bat is resting. (B) The maximum increases in Tsk after the flight events. The grey circles were the data of individual bats. C, D A comparison of the total time length (duration) and the rate of the Tsk changes between the Tsk rising and decaying periods. E, F, G The maximum increases in Tsk seem to be negatively related to the rising time, positively related to the decay time, but unrelated to the flight time. Note, flight time here is the sum of separated flight bouts within the rise time window. For the statistical tests of E and G, the outlier data point was excluded. Note, we had a very small sample size (individuals) that probably limited our ability to detect a statistical significance for data in E and F. The sample size for each group is indicated by the associated number

Subsequently, we analyzed the correlation between the maximum increase in Tsk and three temporal parameters: the rise time, the decay time, and the flight time. We found that the maximum increase in Tsk was negatively related to the rise time, after excluding one outlier data point (Fig. 4E; Pearson correlation, R = -0.87, P = 0.011). In other words, the faster the Tsk rises, the greater the maximum increase in Tsk. There is a strong trend that the greater the maximum increase in Tsk, the longer the decay time (Fig. 4F). However, there was no indication that the maximum increase in Tsk correlated with the total flight time (Fig. 4G; Pearson correlation, R = -0.09, P = 0.85).

Body temperature and flight behavior of free-ranging H. armiger in the field

To study body temperature dynamics in the wild, 10 H. armiger individuals were tagged and released (see “Methods”). In total, we recovered dataloggers from five individuals, four of which had data. Nevertheless, we only identified clear flight bouts from two of these four bats. We plotted the synchronized Tsk and acceleration data for a bat with clear flight bouts (Fig. 5A, B). Figure 5B shows a zoomed-in view of the flight bouts from the field and the laboratory recording. We found that the wingbeat frequencies were similar in these recordings (Fig. 5C; Wilcoxon rank-sum test, z-value = 0.46, P = 0.64). By contrast, the flight bouts in the field were characterized by acceleration with greater amplitude than those in the laboratory (Fig. 5C; Wilcoxon rank-sum test, z-value = -7.6, P < 0.001), although the causes or the implications of this difference are unknown.

Fig. 5
figure 5

Measuring body temperature and flight behavior of free-ranging bats in the field. A Example recordings of Tsk and flight-induced accelerations in a bat with identifiable flight bouts from the field. B Zoomed-in views of flight bouts from the field (highlighted in green of A) and from the laboratory. C Comparisons of the wingbeat frequency and the peak amplitude of z-acceleration between the field and laboratory recordings. The grey circles indicate the data of individual bats. The sample size for each group is indicated by the associated number


Methods for measuring the body temperature of bats

To date, three main techniques have been used to measure the body temperature of bats: thermocouples, light-weight temperature sensors, and thermal infrared imaging cameras. In recent years, light-weight temperature sensors have become a popular and dominant method for studying bats’ body temperature (Fig. 2A). Specifically, for research conducted after 2000, temperature sensors were used in 73% of the studies. One advantage of the temperature sensor, compared to the traditional thermocouples, is its capability for recording the body temperature of freely behaving animals continuously. Although the thermal infrared imaging method also allows measuring the body temperature of freely behaving animals, these cameras are far more expensive. Previous studies have shown that in small animals the Tsk can accurately represent the core body temperature, particularly when the Tsk was measured subcutaneously as in our case [28]. Indeed, our limited calibration data showed that there were on average only 0.4 ºC difference between the core body temperature and Tsk measured subcutaneously (Additional file 1: Fig. S1B). Note, the Tsk measurements are closely related to, but can be different from, the core body temperature as measured rectally [5, 28, 29]. One critical factor that affects the accuracy of the Tsk for representing the core Tb is the air temperature. Thus, a second temperature sensor for measuring the air temperature should be added for studying bats in an environment where the air temperature fluctuates across the recording period.

Effects of flight on body temperature of bats

Bats are the only mammals capable of powered flight. The unique flight capability raises the question of how flapping flight affects bats’ body temperature [9, 30]. Because flight in bats requires on average twice the energy of running mammals of similar body size, both the respiratory rate and the heart rate increase dramatically during the flight [31]. The high metabolic rate of flapping flight in bats poses a danger of overheating [3]. Here, we provide evidence that flight induces an increase in the body temperature of bats, with an amount of 3.4 °C (between 1.9 and 5.3 °C for different individuals) in the laboratory. Assessing the effects of flight on body temperature in the field is more challenging, due to the limited acceleration data available. Nevertheless, as shown in Fig. 5A, it seems that the maximum increase in the body temperature in the free-ranging bats in the field (~ 3 °C) is similar to that in the laboratory. A median of 3.4 °C increase in Tsk associated with flight is similar to reports for some bat species (~ 4 °C) [30], as well as for some birds [32], but slightly smaller than that reported for Phyllostomus hastatus of about 5 °C [4]. If we use the lowest and the median Tsk during the recording session as a reference for calculating the maximum increase in Tsk due to the flight, the median values would be 5.3 and 3.8 °C, respectively. Thus, they become closer to those reported for other bat species.

The maximum Tsk recorded for the bats in the laboratory was narrowly centered at 40 °C (between 38.5 and 40.9 °C). Previous research showed that the Tsk is usually lower than the Tb, but the maximum difference is no greater than 3.3 °C [28]. It was also shown that at an air temperature greater than 20 °C that is true for our measurements, the actual difference between Tsk and Tb would be smaller than 2 °C [29]. Thus, it seems that the bats actively maintained the maximum body temperature below the lethal level of 44–45 °C [31]. Again, the observed maximum body temperatures during the flight are consistent with flying birds [32], as well as a range of non-flying mammals [28].

Several mechanisms have been proposed to facilitate heat dissipation of flying bats to maintain the body temperature below the lethal level, such as the special membrane structure of bat wings and the increased airflow during wing flapping [3]. One interesting finding from this study is that the longer the rise time, the smaller the maximum increase in Tsk. This finding suggests that the bats can potentially slow down the body temperature increase with intermittent flights, as compared with a continuous flight. Indeed, it has been observed that some bat species, such as Pteropus poliocephalus, cannot maintain continuous flight for even a few minutes at an air temperature > 24 ºC [33], although it is unknown whether H. armiger similarly becomes hyperthermic with prolonged flight. H. armiger is a bat species that scan and detect fluttering insects from perches. This perch searching behavior is suggested to be a strategy in conserving energy and serves to compensate for the energetically expensive hunting with the short sallying flights from a perch [34]. Here, we suggest that, in addition to optimizing the energy efficiency, perch-hunting behavior that results in intermittent flights may function as a thermoregulatory strategy to avoid fatal hyperthermia.


In this study, we made synchronized recordings of the body temperature and flight behavior with onboard dataloggers in a perch-hunting bat species. Our data provide evidence that flight affects the body temperature of flying bats and bats regulate the maximum body temperature within a narrow range below the lethal values of hyperthermia. The skin temperature changes induced by flight nicely corroborated earlier studies, thus providing putative evidence that skin temperature measurements used with onboard miniature temperature sensors can be a useful tool for studying flying bat physiology. This study also revealed one interesting and potential behavioral strategy that can be used by the bats to control the body temperature, namely the intermittent flight associated with the perch-hunting behavior of some species of bats. Furthermore, we want to emphasize that bat species that use perch-hunting strategies for foraging, mainly those from the Rhinolophidae and Hipposideridae families, were least studied for thermophysiology, as our literature survey reveals. Lastly, we presented pilot data to show that these dataloggers can be applied to study the effects of flight on body temperature in freely ranging bats in the real world.


Animals and dataloggers

All experiments were performed with permission from the National Research Council of Thailand (NRCT), with the consent of the Department of National Park, Wildlife and Plant Conservation (DNP)—permit number 0002/2865. In total, 18 Hipposideros armiger bats were caught in the Satun cave in Thailand (6°59′34.32"N, 100° 8′26.48"E using hand nets, and each bat was tagged with a miniature data logger (Vesper, ASD Inc. Israel, see for technical specs). The vespers included a synchronized temperature sensor (LMT86, Texas Instruments, Texas, USA) and a 3D accelerometer (Inversense, inc). The device was mounted on the back of the bats right in between the shoulders using surgical cement (Permatype inc.). The temperature sensor, protruding from the device was inserted subcutaneously by making a slit in the skin (0.5 cm long, which was glued using the cement). The temperature sensor sampled the data at a rate of approximately 1200 Hz and the acceleration sensor sampled the data at a rate of approximately 40 Hz. 10 bats were studied in the field and these bats were also mounted with a telemetry unit (Holohil Systems Ltd. Carp, Ontario, Canada) to ease the finding of the GPS device after it falls off the bats. H. armiger is one of the largest echolocating bat species and we only tagged individuals that weighed > 50 g. The device’s average weight was 5 g, thus accounting for ≤ 10% additional loading on the animal’s weight, which was already shown to be feasible for a bat to carry while commuting and foraging [35, 36]. The remaining 8 bats were used for the laboratory study. Here, the animals were released in a 3 × 2 × 2 m3 room and encouraged to fly for a few minutes typically. In between the experiments in the laboratory, the bats were kept in handbags at room temperature and they were released at the capture site on the same day or the next day after removing the tags. They were fed mealworms and offered water. For the field experiment, tags were retrieved within 10 days either by collecting them from the cave’s ground or by recapturing the bats. To our best knowledge, tags did not remain on the bats for more than 10 days.

We validated that the z-acceleration measurements are correlated with wingbeat in four flying bats (Additional file 1: Fig. S2). As shown in Additional file 1: Fig. S2A, a multi-video camera system revealed a wingbeat frequency of 8.2 ± 0.6 Hz in a bat flying in a large flight room (5.5 × 4.5 × 2.5 m). Also, Additional file 1: Fig. S2B shows that the Z-acceleration data are synchronized with the wingtip tracking in another bat species where we had both video and acceleration data [37]. The details for the multi-camera tracking system and motion analysis can be found in a previous study.

Data analysis

All data were analyzed in MATLAB with customer scripts (version 2018b, Mathworks, Natick, MA, USA). The raw data from which specific measurements were made are shown in Fig. 1A–C. Since recordings of the temperature and acceleration data are synchronized with the same sampling clock, the sampling time was used as a reference to examining the relationship between body temperature and flight behavior. For acceleration data, we only analyzed the z-axis recording which reflects the wingbeat cycles [38]. To calculate the wingbeat frequency, short-time Fourier transformation of the z-axis acceleration data was used and the outputs were averaged across time, from which the wingbeat frequency was estimated as the frequency peak (Fig. 1D; 128-point window size with 90% overlapping between adjacent frames). These settings give a frequency resolution of about 0.3 Hz. Wingbeat frequency was estimated for each identified flight bout and manually inspected to confirm the quality. Assuming a flight speed of the bat in the laboratory is 3 m/s, and a body mass of 60 g, the wingbeat frequency predicted based on scaling-laws for our bats is 7.9 Hz [39], which is consistent with empirical measurements from a recent study [40].

We identified the flight bouts from the z-axis acceleration data with a fixed amplitude threshold after applying a 2 Hz high-pass Butterworth filter (4th order) to prevent low-frequency noise. The amplitude threshold was set to 1000 and 5000 for the laboratory and field acceleration data, respectively. We used a higher amplitude threshold for the field recording because the recordings in the field were much greater in amplitude than those in the laboratory. A flight bout was defined as a section of continuous oscillation with the absolute amplitude of the samples exceeding the specified amplitude threshold and its duration no shorter than 4 s. This artificially set duration threshold guaranteed at least 160 data samples (40 Hz sampling frequency for the acceleration data) to perform a 128-point (FFT size) spectral analysis. Within the flight bout, the duration of continuous samples with their amplitude lower than the specified amplitude threshold is no longer than one second. The processes for identifying the flight bouts are essentially the same for identifying acoustic events as described in previous studies [41, 42]. With these criteria, 18 flight bouts had a wingbeat frequency below 5 Hz, which is unusually slow for our bats (see above). Furthermore, despite a dominant lower frequency peak, these low wingbeat flight bouts often contain a secondary frequency peak above 5 kHz of yet smaller amplitudes. Thus, these slow-wingbeat flights were excluded from further analysis.

Literature survey

To better understand the progression of the techniques applied for measuring bat body temperature over the years, we performed a systematic literature survey on studies of the body temperature in bats. Firstly, we used combinations of keywords to identify relevant studies from the database Web of Science ( Specifically, in the Advanced Search window, the search terms TS = ("bats" AND "body temperature") OR TS = ("bats" AND "core temperature") OR TS = ("bats" AND "skin temperature") OR TS = ("bats" AND "active temperature") were used, which returned 509 studies. Subsequently, we went through the title, abstract, and keywords of each study, and excluded 347 studies. We excluded these studies either because no body temperature data were collected or that the study subjects were not bats. Additionally, we excluded one study that the body temperature was measured after scarifying the animal, and six studies in which the body temperature was measured for anesthetized animals. Lastly, we supplemented the identified literature list with relevant studies from our personal library. In total, we identified 179 studies on the body temperature of bats (Additional file 1: Table S1).

Availability of data and materials

The data sets used and analyzed during the current study are available from the corresponding author on request.


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We thank A. Boonman for technical assistance during the project.


JL was funded by the National Natural Science Foundation of China (31970426) and a Career Development Award from the Human Frontier Science Program (CDA00009/2019-C). SG was supported by the Sagol School of Neuroscience, Tel Aviv University.

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SG collected the data, with supports from SB; HY performed the literature survey; OE calibrated the loggers; JL and HY analyzed the data, with support from YY; JL and YY wrote the manuscript. YY supervised the project. All authors read and approved the final manuscript.

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Correspondence to Jinhong Luo or Yossi Yovel.

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Supplementary Information

Additional file 1: Fig. S1.

Calibrated measurements of the skin temperature, core body temperature, and air temperature of a flying H. armiger in the laboratory. Fig. S2. Calibrations of the accelerometers with flying bats. Table S1. The List of studies on the body temperature of bats.

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Luo, J., Greif, S., Ye, H. et al. Flight rapidly modulates body temperature in freely behaving bats. Anim Biotelemetry 9, 45 (2021).

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