Activity patterns of Pipistrelle bats (Pipistrellus pipistrellus) in north-east Scotland

Pipistrellus pipistrellus emerge from their nursery roosts in north-east Scotland about 35 minutes after sunset, at light intensities of between 15 and 35 lux. Cloud cover, windspeed, ambient temperature, rain, light mist and moonlight have no apparent effect on the time or pattern of emergence. Throughout pregnancy and lactation, emergence lasts for about an hour. After weaning, when the adult females have left the roost, their young take about 40 minutes to emerge. The average rate of initial emergence is proportional to colony size, and the maximum rate of emergence occurs half way through the exodus.
During pregnancy in May and June most bats leave the roost once each night soon after dusk and return between midnight and dawn. After parturition in late June the activity pattern becomes bimodal and the numbers of bats outside the roost show peaks after dusk and immediately before dawn. There is intermittent activity in the vicinity of the roost all night and bats make two or three flights each night. After weaning in August the activity pattern gradually ceases to be bimodal, and the number of flights per bat falls to between one and two. The average time spent outside the roost varies between 2–5 and 5 hours during the summer. The recorded activity patterns of night-flying insects are all bimodal, with peaks after dusk and before dawn, corresponding with the maximum number of bats outside the roost during lactation.     

犬蝠夜栖息地及夜栖息巢特征的初步研究

<正>大多数种类的蝙蝠不会整个晚上都进行觅食,通常在觅食期间有一段长短不一的时间停留在临时地休息,此为夜栖息行为(Hatfield,1937;Krutzsch,1954;Barbour and Davis,1969;Kunz,1973,1974;Hirshfeld et al.,1977)。蝙蝠在夜栖息地进食(Vaughan,1976;Funakoshi and Maeda,2003)、休息并消化食物(Brigham,1991;Funakoshi and Maeda,2003),甚至社会交流(Kunz,1982;Kunz and Lumsden,2003)。不同种类的蝙蝠     

Day roost selection in female Bechstein's bats (Myotis bechsteinii): a field experiment to determine the influence of roost temperature

The decision where to live has far-reaching fitness consequences for animals. In contrast to most other mammals or birds that use sheltered nest sites, female Bechstein's bats frequently switch day roosts during one breeding season, and therefore must often decide where to spend the day. Selecting the right roost is important, because roost quality, e.g. microclimatic condition, influences survival and reproduction in bats. Although thermal factors are very important for the quality of roosts occupied by bats, whether bats base their day roost selection directly on roost temperature has not been tested in the field. Over one summer, we examined and tested the roost choice of 21 individually marked female Myotis bechsteinii living in one maternity colony. In a field experiment, we allowed the bats to choose between relatively warm versus cold bat boxes, while controlling for site preferences. We expected females to exhibit a preference for warm roosts during pregnancy and lactation to accelerate gestation and shorten the period of growth of their young. Roost occupancy over 160 census days reflected significant temperature differences among 89 surveyed roosts (14 tree holes and 75 bat boxes), and preferences changed with the season. Females significantly preferred cold roosts before parturition, whereas post-partum, they significantly favoured warm roosts. Temperature preferences were independent of the roost site, and thus roost selection was based directly on temperature. Boxes with significantly different daytime temperatures did not differ significantly at night. Consequently, bats would have to spend at least 1 day in a new roost to test it. Information transfer among colony members might facilitate knowledge of roost availability. Access to many roosts providing different microclimates is likely to be important for successful reproduction in the endangered Bechstein's bat.     

Roost selection by Formosan leaf-nosed bats (Hipposideros armiger terasensis)

Patterns of roost use by Formosan leaf-nosed bats (Hipposideros armiger terasensis) were studied from November 1998 to April 2000. Structural characteristics, microclimates, and disturbance levels of 17 roosts used by H. a. terasensis and 15 roosts either used by other bat species (2) or not occupied by any bat species were compared. Roosts used by these bats were significantly larger in size and had greater areas covered by water compared to unused roosts. Entrances of active roosts were more likely to be east-west oriented. Hibernacula had lower entrances and ceilings than did roosts used only in summer. Higher temperatures were recorded in non-breeding roosts than in breeding roosts, but temperature gradients in these two types of roosts did not differ. In winter, hibernacula were warmer, and the temperature fluctuated less than in non-hibernacula. The relative humidities in summer roosts and hibernacula were nearly 100%. Disturbance levels were significantly higher in non-breeding roosts than in breeding roosts, and in non-hibernacula than in hibernacula. These results suggest that the Formosan leaf-nosed bats are selective of their roosts, but the pattern of their roost selection differs from those reported for bats of temperate regions. The reasons for such differences may be related to differences in body size, behavior, and reproductive strategy of the Formosan leaf-nosed bats living in a subtropical climate in Taiwan.     

Roost use by long-tailed bats in South Canterbury: examining predictions of roost-site selection in a highly fragmented landscape

We studied the roosting ecology of the long-tailed bat (Chalinolobus tuberculatus) during the springautumn months from 1998–2002 at Hanging Rock in the highly fragmented landscape of South Canterbury, South Island, New Zealand. We compared the structural characteristics and microclimates of roost sites used by communally and solitary roosting bats with those of randomly available sites, and roosts of C. tuberculatus occupying unmodified Nothofagus forest in the Eglinton Valley, Fiordland. Roosting group sizes and roost residency times were also compared. We followed forty radio-tagged bats to 94 roosts (20% in limestone crevices, 80% in trees) at Hanging Rock. Roosts were occupied for an average of 1 day and 86% were only used once during the study period. Colony size averaged 9.8 ± 1.1 bats (range 2–38) and colonies were dominated by breeding females and young. Indigenous forest, shrubland remnants and riparian zones were preferred roosting habitats. Communally roosting bats selected roosts in split trunks of some of the largest trees available. Selection of the largest available trees as roost sites is similar to behaviour of bat species occupying unmodified forested habitats. Temperatures inside 12 maternity roosts measured during the lactation period were variable. Five roosts were well insulated from ambient conditions and internal temperatures were stable, whereas the temperatures inside seven roosts fluctuated in parallel with ambient temperature. Tree cavities used by bats at Hanging Rock were significantly nearer ground level, had larger entrance dimensions, were less well insulated, and were occupied by fewer bats than roosts in the Eglinton Valley. These characteristics appear to expose their occupants to unstable microclimates and to a higher risk of threats such as predation. We suggest that roosts at Hanging Rock are of a lower quality than those in the Eglinton Valley, and that roost quality may be one of the contributory factors in the differential reproductive fitness observed in the two bat populations. The value of introduced willows (especially Salix fragilis) as bat roosts should be acknowledged. We recommend six conservation measures to mitigate negative effects of deterioration of roosting habitat: protection and enhancement of the quality of existing roosts, replanting within roosting habitat, provision of high quality artificial roosts, predator control, and education of landowners and statutory bodies.     

The effect of logging on fission-fusion behaviour of tree-dwelling bats explored by an agent-based model

Logging is one of the greatest threats to global biodiversity, while forests are one of the most important habitats for bats. Bats that roost in tree cavities require a large number of potential roosts due to their frequent roost switching. However, the density of tree cavities and hollows sufficient to sustain large populations of bat species in forests is unknown. The fission-fusion dynamics of bat groups in forest environment is associated with ritualised dawn swarming behaviour at potential tree cavities that serves to exchange information in a non-centralised decision-making process. We used a computer model based on the swarm algorithm, SkyBat, that resembles this complex process and aimed to determine how population size changes over time when cavity trees are removed from roosting territory of the local population of Leisler's bats (Nyctalus leisleri), which inhabit a forest habitat in Central Europe. Simulations revealed that social bonds between bats, maintained by frequent switching among groups, play an important role in this highly dynamic system. When strong social contact was not considered, reducing the original number of trees with cavities (20 cavities × ha⁻¹) to 50% was still acceptable to bats, but further interventions and/or increased demand for social contact would have led to local extinction of the species. Results suggest that potential bat roosts in mature forest stands should be preserved as much as possible and that non-intensive logging and management can be beneficial to tree-dwelling bats.     

Sociality influences thermoregulation and roost switching in a forest bat using ephemeral roosts

In summer, many temperate bat species use daytime torpor, but breeding females do so less to avoid interferences with reproduction. In forest‐roosting bats, deep tree cavities buffer roost microclimate from abrupt temperature oscillations and facilitate thermoregulation. Forest bats also switch roosts frequently, so thermally suitable cavities may be limiting. We tested how barbastelle bats (Barbastella barbastellus), often roosting beneath flaking bark in snags, may thermoregulate successfully despite the unstable microclimate of their preferred cavities. We assessed thermoregulation patterns of bats roosting in trees in a beech forest of central Italy. Although all bats used torpor, females were more often normothermic. Cavities were poorly insulated, but social thermoregulation probably overcomes this problem. A model incorporating the presence of roost mates and group size explained thermoregulation patterns better than others based, respectively, on the location and structural characteristics of tree roosts and cavities, weather, or sex, reproductive or body condition. Homeothermy was recorded for all subjects, including nonreproductive females: This probably ensures availability of a warm roosting environment for nonvolant juveniles. Homeothermy may also represent a lifesaver for bats roosting beneath loose bark, very exposed to predators, because homeothermic bats may react quickly in case of emergency. We also found that barbastelle bats maintain group cohesion when switching roosts: This may accelerate roost occupation at the end of a night, quickly securing a stable microclimate in the newly occupied cavity. Overall, both thermoregulation and roost‐switching patterns were satisfactorily explained as adaptations to a structurally and thermally labile roosting environment.     

Effects of Hierarchical Roost Removal on Northern Long-Eared Bat (Myotis septentrionalis) Maternity Colonies

Forest roosting bats use a variety of ephemeral roosts such as snags and declining live trees. Although conservation of summer maternity habitat is considered critical for forest-roosting bats, bat response to roost loss still is poorly understood. To address this, we monitored 3 northern long-eared bat (Myotis septentrionalis) maternity colonies on Fort Knox Military Reservation, Kentucky, USA, before and after targeted roost removal during the dormant season when bats were hibernating in caves. We used 2 treatments: removal of a single highly used (primary) roost and removal of 24% of less used (secondary) roosts, and an un-manipulated control. Neither treatment altered the number of roosts used by individual bats, but secondary roost removal doubled the distances moved between sequentially used roosts. However, overall space use by and location of colonies was similar pre- and post-treatment. Patterns of roost use before and after removal treatments also were similar but bats maintained closer social connections after our treatments. Roost height, diameter at breast height, percent canopy openness, and roost species composition were similar pre- and post-treatment. We detected differences in the distribution of roosts among decay stages and crown classes pre- and post-roost removal, but this may have been a result of temperature differences between treatment years. Our results suggest that loss of a primary roost or ≤ 20% of secondary roosts in the dormant season may not cause northern long-eared bats to abandon roosting areas or substantially alter some roosting behaviors in the following active season when tree-roosts are used. Critically, tolerance limits to roost loss may be dependent upon local forest conditions, and continued research on this topic will be necessary for conservation of the northern long-eared bat across its range.     

Summer tree roost selection by Rafinesque's big-eared bat

Roost requirements of most North American forest bats are well-documented, but questions remain regarding the ultimate mechanisms underlying roost selection. Hypotheses regarding roost selection include provision of a stable microclimate, space for large colonies, protection from predators, and proximity to foraging habitat, among others. Although several hypotheses have been proposed, specific mechanisms likely vary by species and geographic region. Rafinesque's big-eared bat (Corynorhinus rafinesquii) commonly roosts in trees with large basal hollows in the Coastal Plain of the southeastern United States. Our objective was to weigh evidence for hypotheses regarding selection of diurnal summer roosts by Rafinesque's big-eared bat at 8 study sites across the Coastal Plain of Georgia, USA. We used transect searches and radiotelemetry to locate roosts and measured 22 characteristics of trees, tree cavities, and surrounding vegetation at all occupied roosts and for randomly selected unoccupied trees. We evaluated 10 hypotheses using single-season occupancy models and used Akaike's information criterion to select the most parsimonious models. We located 170 tree roosts containing approximately 870 bats for our analysis. The best supported model predicted bat presence from cavity size, interior wall texture, and number of entrances. Because large cavities allow bats to fly and smooth walls impede attacks by terrestrial predators, our results are consistent with the hypothesis that bats select roosts that allow them to evade predators. However, data on predation rates are needed for a conclusive determination. Because trees suitable as roosts for Rafinesque's big-eared bat are rare in the landscape, protection of suitable forested wetland habitat is essential to provide current and long-term roost tree availability. © 2012 The Wildlife Society.     

Social networks based on frequency of roost cohabitation do not reflect association rates of Myotis lucifugus within their roosts

Bats are a group of mammals well known for forming dynamic social groups. Studies of bat social structures are often based upon the frequency at which bats occupy the same roosts because observing bats directly is not always possible. However, it is not always clear how closely bats occupying the same roost associate with each other, obscuring whether associations result from social relationships or factors such as shared preferences for roosts. Our goal was to determine if bats cohabitating buildings were also found together inside roosts by using anti‐collision technology for PIT tags, which enables simultaneous detection of multiple tags. We PIT‐tagged 293 female little brown myotis (Myotis lucifugus) and installed antennas within two buildings used as maternity roosts in Yellowstone National Park. Antennas were positioned at roost entryways to generate cohabitation networks and along regions of attic ceilings in each building to generate intraroost networks based on proximity of bats to each other. We found that intraroost and cohabitation networks of buildings were significantly correlated, with the same bats tending to be linked in both networks, but that bats cohabitating the same building often roosted apart, leading to differing assessments of social structure. Cohabitation rates implied that bats associate with a greater number of their roost‐mates than was supported by observations within the roost. This caused social networks built upon roost cohabitation rates to be denser, smaller in diameter, and contain nodes with higher average degree centrality. These results show that roost cohabitation does not reflect preference for roost‐mates in little brown myotis, as is often inferred from similar studies, and that social network analyses based on cohabitation may provide misleading results.     

Rediscovery of short-tailed bats (

Short-tailed bats (Mystacina sp.) were rediscovered in Nothofagus dominant rainforest in the Eglinton Valley in February 1997, representing the first records of these bats in Fiordland since 1871. Breeding females, adult males and juveniles were captured. This paper presents preliminary observations of taxonomy, echolocation calls, population size, habitat use, activity patterns, home range size, movements, roosting, and singing behaviour. Compared to lesser short- tailed bats (M. tuberculata) on Codfish and Little Barrier Islands, the Fiordland bats were heavier, had larger wings and smaller ears, and were sexually dimorphic. The Mystacina echolocation calls were of low intensity (quiet), making them difficult to detect. Call durations in free-flying bats were only 1.0-2.9 ms long. In a comparative trial the majority of calls that were detected at 25 kHz using the Batbox III bat detector were not recorded at 40 kHz, indicating that there was little overlap with the calls of long-tailed bats (Chalinolobus tuberculatus). In February, roosting groups numbered from 107 to 279 individuals and the bats ranged over 130 km(2) of the valley. Bats began emerging c. 20 minutes after sunset and were active at the roost sites throughout the night. Radio-tagged bats were active for an average of 372 minutes at a time. All roosts were in large diameter (67-146 cm dbh) red beech (N. fusca) trees.     

Influence of night length on home range size in the northern bat Eptesicus nilssonii

The northern bat Eptesicus nilssonii is widespread in Fennoscandia, with breeding populations well above the Arctic Circle. I studied this species at its extreme northern limit, at 69°N in Norway. I radio-tracked 17 bats from 2 maternity roosts during 2003–2006 to study the influence of the midnight sun and increasing lengths of darkness on activity (time spent out of roost) and home range size. Activity and home range was highly correlated with night length (light intensity); both increasing progressively with season. Bats were classified into 3 groups based on the time of the season they were tracked (basically July, August and September–October); short activity (average 1.57 h) and small home range (average 0.91 km²), medium activity (3.69 h) and medium-sized home range (4.58 km²), and long activity (4.80 h) and large home range (17.2 km²). Bats visited roosts several times during the night, and the duration of roost visits increased significantly by group. The number of periods out of roost increased from the first to the second group (1.45 vs. 2.36 flight periods per night), but insignificantly to the third group (2.37 flights). The most significant increase in activity and home range was associated with the first flight of juveniles in early August. These bats appeared to have a threshold level of around 1700 lux for activity out of roost, with little difference between light levels at emergence and return (the second group returned in significantly poorer light than they emerged in). Although the northern bat at this extreme latitude had adapted to the ambient light conditions, the bright nights under the midnight sun and the short season strongly reduced their window of opportunity for activity and may possibly reduce survival and reproductive success.     

Non-parametric entrainment by natural twilight in the microchiropteran bat, Hipposideros speoris inside a cave

The study aimed to determine the influence of repeated natural dawn and dusk twilight pulses in entraining the circadian flight activity rhythm of the microchiropteran bat, Hipposideros speoris, free-running in constant darkness in a natural cave. The bats were exposed to repeated dawn or dusk twilight pulses at eight circadian phases. All bats exposed to dawn twilight pulses were entrained by advancing transients, and the stable entrainment was reached when the onset of activity occurred about 12 h before the lights-on of the pulses, irrespective of the initial phase at which the bats were exposed to twilight. All bats exposed to dusk twilight pulses, however, were entrained by delaying transients, and the stable entrainment was reached when the onset of activity occurred about 1.6 h after the lights-on of the pulses. The entrainment caused by dawn and dusk twilight pulses is discussed in the context of the postulated two photoreceptors: the short wavelength sensitive (S) photoreceptors mediating entrainment via dusk twilight, and the medium wavelength sensitive (M) photoreceptors mediating entrainment via dawn twilight.     

Non‐Parametric Entrainment by Natural Twilight in the Microchiropteran Bat,Hipposideros Speoris Inside a Cave

The study aimed to determine the influence of repeated natural dawn and dusk twilight pulses in entraining the circadian flight activity rhythm of the microchiropteran bat, Hipposideros speoris, free‐running in constant darkness in a natural cave. The bats were exposed to repeated dawn or dusk twilight pulses at eight circadian phases. All bats exposed to dawn twilight pulses were entrained by advancing transients, and the stable entrainment was reached when the onset of activity occurred about 12 h before the lights‐on of the pulses, irrespective of the initial phase at which the bats were exposed to twilight. All bats exposed to dusk twilight pulses, however, were entrained by delaying transients, and the stable entrainment was reached when the onset of activity occurred about 1.6 h after the lights‐on of the pulses. The entrainment caused by dawn and dusk twilight pulses is discussed in the context of the postulated two photoreceptors: the short wavelength sensitive (S) photoreceptors mediating entrainment via dusk twilight, and the medium wavelength sensitive (M) photoreceptors mediating entrainment via dawn twilight.     

Roosting and Foraging Social Structure of the Endangered Indiana Bat (Myotis sodalis)

Social dynamics are an important but poorly understood aspect of bat ecology. Herein we use a combination of graph theoretic and spatial approaches to describe the roost and social network characteristics and foraging associations of an Indiana bat (Myotis sodalis) maternity colony in an agricultural landscape in Ohio, USA. We tracked 46 bats to 50 roosts (423 total relocations) and collected 2,306 foraging locations for 40 bats during the summers of 2009 and 2010. We found the colony roosting network was highly centralized in both years and that roost and social networks differed significantly from random networks. Roost and social network structure also differed substantially between years. Social network structure appeared to be unrelated to segregation of roosts between age classes. For bats whose individual foraging ranges were calculated, many shared foraging space with at least one other bat. Compared across all possible bat dyads, 47% and 43% of the dyads showed more than expected overlap of foraging areas in 2009 and 2010 respectively. Colony roosting area differed between years, but the roosting area centroid shifted only 332 m. In contrast, whole colony foraging area use was similar between years. Random roost removal simulations suggest that Indiana bat colonies may be robust to loss of a limited number of roosts but may respond differently from year to year. Our study emphasizes the utility of graphic theoretic and spatial approaches for examining the sociality and roosting behavior of bats. Detailed knowledge of the relationships between social and spatial aspects of bat ecology could greatly increase conservation effectiveness by allowing more structured approaches to roost and habitat retention for tree-roosting, socially-aggregating bat species.     

Night roosting and the nocturnal time budget of the little brown bat,Myotis lucifugus: Effects of reproductive status,prey density,and environmental conditions

Summary The insectivorous bat Myotis lucifugus typically apportions the night into two foraging periods separated by an interval of night roosting. During this interval, many bats occupy roosts that are used exclusively at night and are spatially separate from maternity roosts. The proportion of the night which bats spend roosting, and thus the proportion spent foraging, vary both daily and seasonally in relation to the reproductive condition of the bats, prey density, and ambient temperature. A single, continuous night roosting period is observed during pregnancy. During lactation, females return to maternity roosts between foraging bouts, and night roosts are used only briefly and sporadically. Maximum use of night roosts occurs in late summer after young become volant. Superimposed upon these seasonal trends is day-to-day variation in the bats' nightly time budget. Long night roosting periods and short foraging periods are associated with cool nights and low prey density. This behavioral response may minimize energetic losses during periods of food scarcity.     

Activity patterns of pipistrelle bats (Pipistrellus pipistrellus) in Oxfordshire

A maternity colony of pipistrelle bats ( Pipisfrellus pipistrellus ), in Oxfordshire, was monitored between 1 March 1989 and 6 October 1989. An infra-red 'automatic bat counter' was installed at the roost, to record the number of bats entering and leaving each minute throughout the night. Air temperature, light intensity at sunset, cloud cover, wind speed and rain were recorded on each night of monitoring. Insect abundance was estimated on 18 nights.
The nightly activity pattern was found to be unimodal in pregnancy, bimodal during lactation and unimodal post-weaning. The mean time that each bat spent outside the roost ranged from 103–483 min, with a mean of 321 min.
Ambient air temperature and length of night were significant factors affecting mean time spent outside the roost. The percentage of the night which the bats spent away from the roost ranged from 22 to 88%, with a mean of 64%. There was a significant positive correlation between ambient air temperature and percentage of the night spent away from the roost. Insect abundance showed no significant correlation with the time that bats spent outside the roost. Wind and rain had no apparent effect on time spent outside the roost.     

Seasonal variation in age,sex, and reproductive status of Mexican free-tailed bats

In North America, Mexican free-tailed bats (Tadarida brasiliensis mexicana) consume vast numbers of insects contributing to the economic well-being of society. Mexican free-tailed bats have declined due to historic guano mining, roost destruction, and bioaccumulation of organochlorine pesticides. Long-distance migrations and dense congregations at roosts exacerbate these declines. Wind energy development further threatens bat communities worldwide and presents emerging challenges to bat conservation. Effective mitigation of bat mortality at wind energy facilities requires baseline data on the biology of affected populations. We collected data on age, sex, and reproductive condition of Mexican free-tailed bats at a cave roost in eastern Nevada located 6 km from a 152-MW industrial wind energy facility. Over 5 years, we captured 46,353 Mexican free-tailed bats. Although just over half of the caught individuals were nonreproductive adult males (53.6%), 826 pregnant, 892 lactating, 10,101 post-lactating, and 4327 nonreproductive adult females were captured. Juveniles comprised 11.5% of captures. Female reproductive phenology was delayed relative to conspecific roosts at lower latitudes, likely due to cooler temperatures. Roost use by reproductive females and juvenile bats demonstrates this site is a maternity roost, with significant ecological and conservation value. To our knowledge, no other industrial scale wind energy facilities exist in such proximity to a heavily used bat roost in North America. Given the susceptibility of Mexican free-tailed bats to wind turbine mortality and the proximity of this roost to a wind energy facility, these data provide a foundation from which differential impacts on demographic groups can be assessed.     

Activity patterns of the Ryukyu flying fox on a subtropical island: responses to seasonal changes in night length

Almost all chiropteran species are nocturnal, but some species are occasionally active during the daytime. We conducted radio-tracking surveys and direct observations of the Ryukyu flying fox, Pteropus dasymallus, in two different habitats—urbanized and forested areas—on a subtropical island from April 2002 to January 2006. We recorded the departure time and return time from/to day roosts as well as behavioral time budgets during the night. The departure and return times shifted in correspondence with seasonal changes in sunset and sunrise times. The Ryukyu flying fox tended to depart earlier in summer when the night length was shorter, suggesting that it adjusts its active period by departing earlier. On the contrary, the amount of foraging performed by the bats in urbanized areas decreased in the summer when fruits of Ficus microcarpa were more abundant, suggesting that the bats adjust their behavioral time budgets in line with local food availability. Daytime activity was observed only in the forested area. In conclusion, the duration of Ryukyu flying fox activity was found to primarily depend on seasonal changes in the light–dark cycle, and this bat may adjust its behavioral time budget according to local food availability and the intensity of human activities.     

Trapped in the darkness of the night: thermal and energetic constraints of daylight flight in bats

Bats are one of the most successful mammalian groups, even though their foraging activities are restricted to the hours of twilight and night-time. Some studies suggested that bats became nocturnal because of overheating when flying in daylight. This is because--in contrast to feathered wings of birds--dark and naked wing membranes of bats efficiently absorb short-wave solar radiation. We hypothesized that bats face elevated flight costs during daylight flights, since we expected them to alter wing-beat kinematics to reduce heat load by solar radiation. To test this assumption, we measured metabolic rate and body temperature during short flights in the tropical short-tailed fruit bat Carollia perspicillata at night and during the day. Core body temperature of flying bats differed by no more than 2°C between night and daytime flights, whereas mass-specific CO(2) production rates were higher by 15 per cent during daytime. We conclude that increased flight costs only render diurnal bat flights profitable when the relative energy gain during daytime is high and risk of predation is low. Ancestral bats possibly have evolved dark-skinned wing membranes to reduce nocturnal predation, but a low degree of reflectance of wing membranes made them also prone to overheating and elevated energy costs during daylight flights. In consequence, bats may have become trapped in the darkness of the night once dark-skinned wing membranes had evolved.