Aerodynamic theory predicts that flight for fixed-wing aircraft requires more energy at low and high speeds compared with intermediate speeds, and this theory has often been extended to predict speed-dependent metabolic rates and optimal flight speeds for flying animals. However, the theoretical U-shaped flight power curve has not been robustly tested for Chiroptera, the only mammals capable of flapping flight. We examined the metabolic rate of seven Seba's short-tailed fruit bats (Carollia perspicillata) during unrestrained flight in a wind tunnel at air speeds from 1 to 7 m s−1. Following intra-peritoneal administration of 13C-labeled Na-bicarbonate, we measured the enrichment in 13C of exhaled breath before and after flight. We converted fractional turnover of 13C into metabolic rate and power, based on the assumption that bats oxidized glycogen during short flights. Power requirements of flight varied with air speed in a U-shaped manner in five out of seven individuals, whereas energy turnover was not related to air speed in two individuals. Power requirements of flight were close to values predicted by Pennycuick's aerodynamic model for minimum power speed, but differed for maximum range speed. The results of our experiment support the theoretical expectation of a U-shaped power curve for flight metabolism in a bat.

Locomotion is a major component of animals' energy expenditure (Dickinson et al., 2000). Flight, in particular, is energetically demanding, and it has been estimated and experimentally confirmed that flight metabolism of bats may be at least twice that of non-volant mammals of comparable size during running (Thomas, 1978; Voigt et al., 2012). This energy expenditure should, according to aerodynamic theory, be strongly speed dependent: a U-shaped curve describes the power–speed relationship, with relatively higher power required for flight at both slowest and fastest speeds than for intermediate speeds (Norberg, 1990; Pennycuick, 1968; Pennycuick, 1975; Pennycuick, 1989; Rayner, 1979; Rayner, 1999; Tucker, 1973). In practice, a variety of factors may influence this theoretical relationship. First, the aerodynamic theory on which this power curve is based was formulated for fixed-wing aircraft, but animals employ flapping flight with potentially many degrees of freedom and hence kinematics of varying complexity (Riskin et al., 2008). As muscle recruitment changes with flight speed, metabolic power could deviate significantly from aerodynamic, mechanical power. Second, the flight power curve formulation assumes steady-state aerodynamics, but many flying animals experience unsteady effects associated with their aerodynamic force production, such as dynamic or delayed stall, attached leading edge vortices, and/or spanwise flow (Birch and Dickinson, 2001; Dickinson, 1996; Muijres et al., 2008; Videler et al., 2004). Additionally, the wings of flying animals are compliant to varying degrees in different taxa, and as a consequence may deform substantially under aerodynamic loading, distinct from flapping motions per se (e.g. Swartz et al., 1996). This compliance, in turn, influences the dynamics of air-speed-dependent force production (Song et al., 2008). Together, these factors suggest that flight power may not be predicted accurately by the conventional model, especially for bats and insects. Predictions may be particularly poor for hovering and slow forward flight, in which unsteady effects are likely to be most pronounced (e.g. Ellington, 1991).

Theory-based predictions for flight energetics have been examined for birds over several decades (e.g. Askew and Ellerby, 2007; Clark and Dudley, 2010; Tobalske et al., 2003; Tucker, 1968), but only rarely for insects (but see Willmott and Ellington, 1997b) or bats (von Busse, 2011; Carpenter, 1985; Carpenter, 1986; Thomas, 1975). In birds, empirical studies of flight metabolism or its correlates have both supported (e.g. Tucker, 1968; Tobalske et al., 2003; Askew and Ellerby, 2007; Clark and Dudley, 2010) and contradicted this hypothesis (Tucker, 1972; Bernstein et al., 1973; Torre-Bueno and Larochelle, 1978; Hudson and Bernstein, 1983; Berger, 1985; Dial et al., 1997; Pennycuick et al., 2000; Ward et al., 2001; Ward et al., 2002; Engel et al., 2006). The diversity of these results could reflect true biological variation among taxa, or some other biological phenomena, such as a body mass dependence of the velocity profile of flight power, with a shallow J-shaped relationship at lower body masses changing to a more U-shaped pattern as body size increases (Voigt and Winter, 1999). However, other factors may contribute to the diverse conclusions observed to date. For example, some studies examined only a limited range of flight speeds (e.g. Bernstein et al., 1973; Hudson and Bernstein, 1983; Ward et al., 2002), and absolute speeds have varied substantially among studies, from hovering (zero forward speed) to 21 m s−1. Measurement technique may also play a key role in defining flight power–velocity relationships. For example, Ward et al. (Ward et al., 2004) assessed flight power by respirometry, doubly labeled water and heat transfer modeling in a single bird species (Sturnus vulgaris) and found a U-shaped relationship when they employed the doubly labeled water method, but a linear increase when using the other measurement techniques.

Few data from bats have contributed to the ongoing debate, largely because it has been difficult to obtain meaningful results from multiple individuals of a single species over a substantial range of flight speeds. In this study we tested quantitatively whether the metabolism of bats is related to speed in a U-shaped manner. We measured flight metabolism using the 13C labeled Na-bicarbonate method (Hambly et al., 2002; Hambly et al., 2004; Voigt and Lewanzik, 2011; Voigt and Lewanzik, 2012) in seven C. perspicillata that flew in a wind tunnel at defined speeds. Based on aerodynamic considerations, we predict that flight metabolism should be higher at low and high speeds than at intermediate speeds.

Study animals

Our study subjects were seven non-reproductive Seba's short-tailed fruit bats [Carollia perspicillata (Linnaeus 1758)] (four males, three females). Animals were maintained in the Animal Care Facilities of Brown University (all components of this study were approved by the Institutional Animal Care and Use Committee at Brown University; IACUC protocol no. 1004016) in a flight room (3.60×2.44×2.18 m). Their diet consisted of fresh fruit and diet formula, following Rasweiler et al. (Rasweiler et al., 2009), with ad libitum access to tap water. Room temperature was 26°C and relative humidity 60%, with a reversed photoperiod of 12 h:12 h dark:light.

Wind tunnel setup

The wind tunnel at the School of Engineering at Brown University is a closed-loop, low-turbulence wind tunnel (Hubel et al., 2009). The test section has a cross-section of 0.60×0.82 m (height × width) and was restricted by mesh frames to a length of approximately 1.50 m. Wind tunnel temperature during experiments was 22.2±1.7°C (mean ± 1 s.d.) and air pressure averaged 101.2±0.4 kPa.

Experimental protocol

We employed the 13C-labeled Na-bicarbonate method (Hambly et al., 2004a; Hambly et al., 2004b; Hambly et al., 2002) modified according to Voigt and Lewanzik (Voigt and Lewanzik, 2011; Voigt and Lewanzik, 2012) for instantaneous measurements of 13C enriched breath. The 13C-labeled Na-bicarbonate method measures the washout of a 13C label previously administered to animals as a sterile and isotonic Na-bicarbonate solution (Hambly et al., 2004a; Hambly et al., 2004b; Hambly and Voigt, 2011; Hambly et al., 2002; Voigt et al., 2010). As the fractional turnover of the label is related to the rate of CO2 production (), it is possible to estimate during flight by measuring the relative loss of 13C in relation to 12C from the body bicarbonate pool during the flight period. Our modified 13C-labeled Na-bicarbonate method used a high-resolution cavity ringdown spectrometer that enabled us to quantify the relative enrichment of 13CO2 in relation to 12CO2 in exhaled breath prior and after the flight interval, applied previously to this species (Voigt and Lewanzik, 2011) and other flying bats (Voigt and Holderied, 2012; Voigt and Lewanzik, 2012; Voigt et al., 2011).

At the beginning of an experimental day, we captured three to five bats in the flight room and transferred them to a 0.5 m3 box in which they were maintained until the experiment commenced. We performed experiments with one bat at a time and one experiment per day for a given bat. However, each bat individual was exposed to six or seven different wind speeds in a random order within the 3 week period of the experiments. After intraperitoneal injection of 100 mg of isotonic Na-bicarbonate solution (0.29 mol l−1; Euriso-Top, Saarbrücken, Germany), we transferred a bat into the 1.4 l respirometry chamber for the pre-flight period. In the chamber, the temperature was kept constant at 30°C. A gas washing bottle filled with NaOH removed the ambient CO2 from the inlet air of the chamber. After label administration, we monitored the increase of 13C enrichment until a plateau value was reached. After the plateau, 13C enrichment declined exponentially. After approximately 5–8 min following the plateau, we released bats singly into the wind tunnel. Trials were performed in random order with respect to wind speed and time of day to avoid any sequential or diurnal effects, respectively, on respirometric measurements. Flight behavior differed among individuals, ranging from almost continuous flight at one location within the test section, to flying at one spot with short bouts of intermittent gliding (non-flapping) in which the bat would be carried backwards by the ambient flow in the test section and would then resume flapping and return to its original position in the test section. Because of these variations in flight behavior, we did not obtain continuous respirometric measurements of a flying bat for a defined wind speed, but instead report net air speed of the wind tunnel. Each individual's flight behavior, however, was consistent throughout the speed range and the mean flight speed of each subject within a trial averaged close to the reported air speed. When bats attempted to land, an investigator interrupted landing approaches to ensure that each subject flew continuously for 1–2 min (mean ± s.d. landing approaches per trial=3.6±4.3).

We recaptured bats after approximately 1–2 min of flight using a handnet. Then, subjects were returned to the respirometry chamber for at least 10 min post-flight. After the experiment, we weighed the bats to the nearest 0.01 g using a precision electronic balance (Denver Instrument, Bohemia, NY, USA). Morphological measurements were made from flight videography captured from directly below the study subjects during experimental flights, from a frame taken from mid-downstroke of flight at 5 m s−1 using ImageJ (http://rsb.info.nih.gov/ij/) following Pennycuick (Pennycuick, 1989). From the wing image, we calculated aspect ratio (wing span squared divided by total wing area) and wing loading (body mass times gravitational force divided by wing area) (Table 1). After experiments, bats were returned to the colony.

Analysis of respirometric and isotopic data

Trials with poor flight performance (e.g. too many landings) or unsteady CO2 levels during pre- or post-flight period, mostly due to high activity of the bat in the respirometry chamber, were excluded from the analysis, and replaced with a subsequent trial for the specific individual and wind tunnel speed. We rejected 24 trials in total (7, 1, 2, 5, 3, 0 and 6 trials for individuals 1 through 7, respectively). We performed blind data analysis to avoid any bias in results, i.e. the person who analyzed the isotopic and respirometric data did not know the air speed of a given trial. For data analysis, we focused on a 20 min period starting approximately 3 min after peak 13C enrichment. This interval consisted of a pre-flight period (~5 min), the flight period (~5 min, including transfers in and out of the wind tunnel) and the post-flight period (~10 min). To calculate the fractional turnover of 13C (kC; min−1) in flying bats, we converted delta values into atom%according to Slater et al. (Slater et al., 2001) and computed linear regressions after the least squares method for the ln-transformed isotopic data against time for the pre- and post-flight period separately. Based on these regressions, we extrapolated the 13C enrichment in the exhaled breath of animals at the onset and end of the flight period. We calculated kC for flying bats according to:
(1)
where xE(13C) is the 13C excess enrichment (in atom%) at the start and stop of the flight trial and t is the flight duration (min). kC (min−1) was multiplied by the total body bicarbonate pool NC (mol) as calculated by the plateau method (Voigt and Lewanzik, 2011), and converted to (ml min 1) by multiplication with 22.4 l mol−1. We applied correction factors based on pre-flight as measured by isotopic and respirometric methods and based on isotopic estimates of during the flight period (Hambly et al., 2004a; Hambly et al., 2004b; Hambly and Voigt, 2011; Hambly et al., 2002; Voigt and Lewanzik, 2011; Voigt and Lewanzik, 2012). A bivariate plot of resting (pre-flight period) supported a high precision of the method (multiple r=0.78). was converted into metabolic power (W) under the assumption that bats exclusively oxidized endogenous glycogen during short flights. Accordingly, we multiplied by 21.1 J ml−1 CO2 produced and divided the result by 60.
Table 1.

Morphological description of experimental subjects

Morphological description of experimental subjects
Morphological description of experimental subjects

Mechanical power prediction

Flight mechanical power arises from the requirement to produce lift and thrust necessary for flight, which creates and thus is embodied in the wake behind a flying animal. To predict mechanical power, we employed Pennycuick's model for vertebrate flight (Pennycuick, 2001). Following helicopter theory, this formulation adopts a momentum jet model for flapping flight mechanics. This model considers the bird or bat as ‘actuator’, a circular disk whose diameter is equal to the wingspan of the animal. The actuator generates downward directed momentum, which must balance the animal's weight in steady level flight. This model ignores the flapping motion of the wings, which generate a pulsed wake. The theoretical estimation of mechanical power is the sum of the induced, parasite and profile power: Pmech=Pind+Ppar+Ppro. Induced power is the rate of work that arises from imparting downward momentum to the air in the production of lift. The parasite power and the profile power are those necessary to overcome the drag of the body and the drag of the wings moving through the air, respectively. In this model, the specific power components are calculated as follows (Pennycuick, 2001):
(2)
where κ is the induced drag factor, m is body mass, g is acceleration due to gravity, ρ is air pressure, Sd is disc area (Sdb2/4) and U is wind speed;
(3)
where A is the flat-plate area A=SbCDb, with Sb equal to body frontal area (Sb=0.00813m2/3, in m2, an empirically determined relationship based on bird flight analysis) and CDb is the body drag coefficient, assigned a value of 0.4; and:
(4)
where Cpp is the profile power constant Cpp=8.4, Pam is the ‘absolute minimum power’, calculated as the minimum value of Pind+Ppar, and AR is the aspect ratio of the wing.

Statistical analysis

To test whether flight metabolism is related to flight speed, we calculated a repeated-measures ANOVA over all individuals and all flight speeds, using Systat (Version 11, Systat Software, Chicago, IL, USA). We conducted two-tailed tests with an alpha value of 5%. Data are presented as means ± 1 s.d. if not stated otherwise.

For statistical testing of the total metabolic rate, we employed a mixed linear model using the GLM procedure in JMP 8.0 (SAS Institute, Cary, NC, USA). The model was constructed including individual as random factor with flight speed as a covariate, and tested for interaction between individual and speed. The relationship between the variable of interest and the covariate were tested as linear and second-order polynomial functions. The best-fit regressions of metabolic power input for the seven individuals were calculated and plotted in OriginPro 8 (OriginLab Corporation, Northampton, MA, USA).

The 13C enrichment in exhaled breath reached peak values after approximately 10–15 min following intraperitoneal injection of 13C-labeled Na-bicarbonate (Fig. 1). usually decreased in resting bats over the course of the experimental period (Fig. 1A). Fractional turnover of the 13C label followed an exponential decline (Fig. 1B).

We calculated both first- and second-order polynomial regression models for the seven individual data sets (Table 2). According to the best fit (highest R2 value, lowest P-value), five out of seven individuals exhibited a U-shaped relationship between metabolic power and air speed, which corresponded to a second-order polynomial fit (Table 2, Fig. 2B–F). Two individuals showed an inverse U-shaped relationship between metabolic rate and air speed; given the lack of predictive theory for such a relationship, we chose to fit the data for these individuals with a linear regression calculated using the least squares method (Table 2, Fig. 2A,G). When data were analyzed by individual, significant regressions were observed in only two subjects (P<0.05; Table 2), two further individuals showed a trend (P<0.1; Table 2). When data for all individuals were pooled, metabolic rate showed a U-shaped relationship with air speed (R2=0.49, P<0.0001, with the metabolic power P=3.05–0.70U+0.10U2); the linear relationship with speed was not significant. Metabolic rate was independent of the number of landings within a trial (repeated-measures ANCOVA, with metabolic rate as a dependent variable, individual as a group factor, number of landings and speed as covariates and number of landings × speed as interaction term; F=1.03, d.f.=10, P=0.44).

Fig. 1.

(A) Concentration (p.p.m.) of 13CO2 (red line) and 12CO2 (black line) in the exhaled breath of Carollia perspicillata during the resting periods of the experiment. The flight period is indicated by a gray box. (B) Atom% enrichment of 13C during the course of the experiment (note logarithmic y-scale). 13C enrichment of exhaled breath at the onset and end of the flight period was extrapolated based on two least squares linear regressions (blue lines) calculated over 3 min of the pre-flight period and 10 min of the post-flight period. The fractional turnover of the 13C label of the flying bat is indicated by the pink dashed line.

Fig. 1.

(A) Concentration (p.p.m.) of 13CO2 (red line) and 12CO2 (black line) in the exhaled breath of Carollia perspicillata during the resting periods of the experiment. The flight period is indicated by a gray box. (B) Atom% enrichment of 13C during the course of the experiment (note logarithmic y-scale). 13C enrichment of exhaled breath at the onset and end of the flight period was extrapolated based on two least squares linear regressions (blue lines) calculated over 3 min of the pre-flight period and 10 min of the post-flight period. The fractional turnover of the 13C label of the flying bat is indicated by the pink dashed line.

Robust statistics show that the medians for metabolic power over all individuals followed a U-shaped curve with respect to speed (Fig. 3). The overall shape of the curve of the medians corresponded to the theoretical prediction derived from Pennycuick's model (Pennycuick, 2001) for flight power from 1 to ~4 m s−1. The model, however, estimates mechanical power, and our study measures metabolic power. We compare these two distinct speed-related power estimates qualitatively; the two y-axes are scaled by eye to best match the value range of flight cost and mechanical flight power because there is no objective, non-arbitrary way to compare the total metabolic power measured empirically with the theoretically predicted mechanical flight power estimates of the model. Pennycuick's model predicts minimum power speed at 5 m s−1 and maximum range speed at ~8.5 m s−1 (Fig. 3). The minimum power speeds derived from the five individuals with U-shaped power curves differed significantly from the minimum power speeds predicted from aerodynamic theory (Mann–Whitney test, h=1, P=0.0025). When only the individuals with significant U-shape and the individual with a trend to a U-shaped relationship are included in the comparison, the significant difference remains (Mann–Whitney test, h=1, P=0.0167). Above 4 m s−1, metabolic rate increased more steeply than mechanical power as predicted by aerodynamic modeling.

Is the bat flight power curve U-shaped?

We investigated the flight speed dependence of power consumption of Seba's short-tailed bats, C. perspicillata, in wind tunnel flight. We used the 13C-labeled Na-bicarbonate method as initially established by Hambly et al. (Hambly et al., 2004a; Hambly et al., 2004b; Hambly et al., 2002), to quantify in bats during unrestrained flight in a wind tunnel over a range of controlled air speeds (1–7 m s−1). A major benefit of the 13C-labeled Na-bicarbonate technique for wind tunnel flight studies is that animals can fly freely without a respirometry mask, and accurate measurements can be made over exercise times of up to several minutes. Thus, these respirometric measurements alter neither the flight behavior of animals nor their characteristic aerodynamics. This technique also made it possible to obtain measurements from a relatively large number of individuals without extended time to train subjects to fly in front of a respirometry mask.

We tested whether metabolic rates follow the predicted U-shaped curve in C. perspicillata, and the degree to which their flight power matched specific predictions of a model developed for birds (Pennycuick, 2001), particularly with regard to two speeds often considered important in the flight ecology community: minimum power flight speed and maximum range speed. Five of seven subjects showed higher metabolic rates at low and high than intermediate flight speeds. In only two individuals was the observed relationship between metabolic rate and flight velocity statistically significant; however, because of the technically challenging nature of these experiments, we collected only a single flight at each speed for each individual, hence the sample size for each individual is quite small. When data for all individuals are pooled, metabolic rate varied significantly with flight velocity, and the best fit to the data was obtained with a second-order polynomial regression. Our results provide support for the U-shaped relationship of flight power to flight speed, but also highlight that individual variation in flight metabolism may be substantial.

Table 2.

Regression coefficients from polynomial regressions for air speed dependence of metabolic power (Fig. 2)

Regression coefficients from polynomial regressions for air speed dependence of metabolic power (Fig. 2)
Regression coefficients from polynomial regressions for air speed dependence of metabolic power (Fig. 2)
Fig. 2.

Relationship between metabolic power (W) and air speed (m s−1) in seven Carollia perspicillata with best-fit regressions (A–G). (H) Summary of data from all trials and individuals.

Fig. 2.

Relationship between metabolic power (W) and air speed (m s−1) in seven Carollia perspicillata with best-fit regressions (A–G). (H) Summary of data from all trials and individuals.

Two kinds of effects could lead to the observed variation of flight metabolism among individuals. One possibility is that individual bats varied in their flight kinematics in subtle ways that were not readily distinguished with the relatively coarse kinematic measurements employed in this study. Flying animals can show significant inter-individual variation in flight mechanics. This phenomenon has been quantified for escape flights in pigeons (Biewener and Dial, 1995) and great tits (Krams, 2002), and weight-carrying in bats (Iriarte-Díaz et al., 2012). This variation extends beyond escape behavior and flying with loads in bats; individual dog-faced fruit bats, Cynopterus brachyotis, show consistent speed-dependent changes in wingbeat kinematics (Hubel et al., 2010). Because bat wings possess a large number of joints under direct muscular control and highly anisotropic, nonlinearly elastic wing membranes with adjustable stiffness (Swartz, 1998; Swartz et al., 1996), bats have greater potential than birds or insects to modulate wing kinematics and hence aerodynamic forces. The second type of effect could be our experimental protocol. Seeking metabolic rate data over as wide a range of flight speeds as possible, we selected bats from our colony that exhibited excellent wind tunnel flight performance. Individuals whose flight performance varied greatly with speed might have been inadvertently deemed ‘poor fliers’, while those with the ability to modulate flight behavior to maintain consistent power consumption in relation to speed would appear as ‘strong fliers’, and would more likely be chosen for wind tunnel experiments. Alternatively, the variation among individuals may have also been influenced by our experimental protocol or some inaccuracies of the 13C-labeled Na-bicarbonate technique. For example, measured metabolic power for a given flight speed may be highly variable within an individual due to the flexible flight behavior of bats. To control for this intrinsic variability, it would have been ideal to perform several experiments for a given flight speed and then calculate average flight metabolic power for each flight speed. However, this was not possible for our experiment because of logistical and time constraints. Another source of inaccuracy is intrinsic to the 13C-labeled Na-bicarbonate technique because 13C enrichments of pre- and post-flight animals are extrapolated based on linear regressions derived from the pre- and post-flight resting period. Small errors in the estimated slopes and intercepts of these regression lines may translate into large biases in the extrapolated 13C enrichments. This may have hampered our ability to record a U-shaped curve in some of the individuals.

Fig. 3.

Metabolic power (W) in relation to air speed in Carollia perspicillata, in comparison to mechanical power versus air speed as predicted by Pennycuick's model. Measured metabolic power is shown in box plots (with minimum and maximum values) for a given air speed, with median values (±median absolute deviation) connected by a solid line. vmp, minimum power speed; vmr, maximum range speed.

Fig. 3.

Metabolic power (W) in relation to air speed in Carollia perspicillata, in comparison to mechanical power versus air speed as predicted by Pennycuick's model. Measured metabolic power is shown in box plots (with minimum and maximum values) for a given air speed, with median values (±median absolute deviation) connected by a solid line. vmp, minimum power speed; vmr, maximum range speed.

Interspecific comparison

Metabolic power has been assessed previously in several bat species, ranging in body mass from ~18 to 800 g (von Busse, 2011; Carpenter, 1985; Carpenter, 1986; Thomas, 1975). Comparison of data from this study with previously published results shows a trend for decrease in mass-specific power with increasing body size, as expected (Fig. 4). Mass-specific metabolic rates of all species studied to date fall in the range of 50 to 150 W kg−1, the same range as observed in birds, and also overlapping the range observed for hawkmoths when mass-specific power is computed from muscle, rather than whole body mass (Willmott and Ellington, 1997a). This comparison also highlights that our study is the first to show a pronounced U-shaped pattern for bats; previous studies suggest a J- or L-shaped curve for metabolic rate–flight speed relationship. These data were collected with respirometric masks, which could have influenced investigators' abilities to obtain data at low and high speeds, limiting exploration of the ascending and descending limbs of the power curve. For larger-bodied species, flight at very low speeds and hovering may be difficult or impossible. We speculate that other species may exhibit a U-shaped power curve when tested with experiments that include higher and/or lower flight speeds, and that our observations on C. perspicillata will not prove unusual.

Fig. 4.

Comparison of mean mass-specific metabolic power (W kg−1) for bats over a range of flight speeds. Data for Eidolon helvum (N=1), Hypsignathus monstrosus (N=1) and Pteropus poliocephalus (N=1 each) (means ± s.e.m.) are from Carpenter (Carpenter, 1985; Carpenter, 1986); data for Phyllostomus hastatus (N=1) and Pteropus gouldii (N=1) (means, calculated from least square fit) are from Thomas (Thomas, 1975); data for Leptonycteris yerbabuenae (N=2) (mean ± s.e.m.) are from von Busse (von Busse, 2011); data for Carollia perspicillata (N=7) (median ± median absolute deviation) are from the present study.

Fig. 4.

Comparison of mean mass-specific metabolic power (W kg−1) for bats over a range of flight speeds. Data for Eidolon helvum (N=1), Hypsignathus monstrosus (N=1) and Pteropus poliocephalus (N=1 each) (means ± s.e.m.) are from Carpenter (Carpenter, 1985; Carpenter, 1986); data for Phyllostomus hastatus (N=1) and Pteropus gouldii (N=1) (means, calculated from least square fit) are from Thomas (Thomas, 1975); data for Leptonycteris yerbabuenae (N=2) (mean ± s.e.m.) are from von Busse (von Busse, 2011); data for Carollia perspicillata (N=7) (median ± median absolute deviation) are from the present study.

Mechanical efficiency

The ratio of mechanical power, the total power of aerodynamic force production, reflected in the wake, to metabolic power, which includes basal metabolism, postural control, etc., is mechanical flight efficiency. This ratio is not necessarily constant over a range of flight speeds, but has the potential to vary with changing wing kinematics, aerodynamic gait, flight mode or muscle efficiency [e.g. intermittent flight in birds reduces the metabolic flight cost (Rayner, 1986; Rayner, 1994; Rayner, 1999); bird pectoralis efficiency changes with flight speed (Morris et al., 2010)]. Based on the theoretical prediction, the mechanical efficiency of C. perspicillata at the minimum power speed is ~12%, close to values previously reported for flying vertebrates. Using the pectoralis muscle as a proxy for the whole organism, Morris and coauthors estimated flight efficiency of cockatiels, Nymphicus hollandicus, at 7–11% (Morris et al., 2010), while somewhat higher values of 12–40% have been proposed for the greater spear-nosed bat, Phyllostomus hastatus, calculated from partial efficiency (Thomas, 1975). Mechanical efficiencies of flying vertebrates are most frequently calculated from metabolic data obtained using respirometry combined with mechanical power estimated from theory (e.g. Bernstein et al., 1973; Dudley and Winter, 2002; Thomas, 1975; Tucker, 1972; Ward et al., 2001), with few authors attempting to employ mechanical power measurements made directly from the flight musculature (but see Morris et al., 2010). These direct measurements yield a lower mechanical power output than the calculations based on aerodynamic theory. However, the method of direct measurements of flight muscle power production may prove inappropriate for bats; unlike birds and insects, which use primarily one or two muscles for force production that are active mostly during the lift-generating downstroke, bats employ multiple muscles for force production and these activity patterns of flight muscles over the wingbeat cycle are complex (e.g. Hermanson and Altenbach, 1985).

Although the minimum power speed predicted by the fixed-wing aerodynamic model lies close to the minimum power speed we observed, beyond this speed, our measurements and the predictions of the model diverge substantially. There are at least two possible explanations for this discrepancy. First, we report metabolic measurements classified by speed as designated by the nominal air speed of the wind tunnel. An individual bat could be flying somewhat faster, advancing with respect to a stationary point in the test section. This would tend to shift the measured curve to the left, and therefore increase the agreement with the predicted curve. Second, wind tunnel flight is not identical to free flight in nature. For example, birds are able to achieve greater speeds in nature than in wind tunnels (Liechti and Bruderer, 2002; Tobalske et al., 1997). If wind tunnel flight incurs an additional energy increment compared with flight in nature, and this increment is greater at higher speeds, we would observe increasing divergence between predicted and observed values with increasing speed. It is also possible, or even likely, that the theoretical model may be appropriate for producing general predictions of bat flight power, but not for precise quantitative estimation. The simplifications and assumptions inherent in this model may more successfully capture adequate detail concerning the physics of bird than bat flight, perhaps in part due to the complex kinematics and wake structure of bat flight (Riskin et al., 2008; Hedenström et al., 2009). The difference between the model and observations may be an empirical indication that this model has not accounted for enough of the relevant energy-consuming phenomena of bat flight to accurately predict minimum power and maximum range speeds for all bats.

In conclusion, we demonstrate that members of the Order Chiroptera exhibit a U-shaped power curve when flying in a wind tunnel over a range of velocities. To assess whether this is true for more species, and to determine the extent of individual variation in the shape of the power curves, studies using the same experimental technique over a wide range of flight speeds with multiple individuals are necessary. Only systematic research can clarify these long-debated questions. Furthermore, experiments to calculate the mechanical power from aerodynamic measurements are called for, to compare theoretical predictions with measurements and to assess mechanical power in animal flight without relying on assumptions based on simplified aerodynamic theory. In this way, improved knowledge of the speed dependence of flight energetics will help advance growing understanding of the ecology and evolution of flying animals.

The authors would like to thank Chen Chiu for her assistance during the experiments and Sohini Ramachandran for her statistical advice. We thank Brock Fenton and an anonymous reviewer for their helpful comments on the manuscript.

FUNDING

Financial support was provided by the National Science Foundation (IOS 0723392 to S.M.S.) and the Air Force Office of Scientific Research (F49620-01-1-0335 and FA9550-12-1-0301 DEF to S.M.S.).

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