Search for: All records

Echolocating bats often encounter clutter as they pursue insect prey. To probe the adaptive behaviors bats employ to mitigate the effects of clutter, this study quantified echolocation call features and head movements of big brown bats (Eptesicus fuscus) as they tracked a moving prey target in the dark. Bats were trained to rest on a perch and track an approaching target for a food reward. Clutter was positioned at different distances and angular offsets from the bat and the path of a moving target. This study hypothesized that bats dynamically adjust call features and head direction to facilitate target localization in the presence of clutter. The results show that bats shortened call duration and interval and increased head movements when the target was close to clutter. The study also revealed that bats increase the production of sonar strobe groups in cluttered environments, which may sharpen sonar spatial resolution. Spectral analysis showed that maximum call power shifted to lower frequencies when clutter was close to the target. These data demonstrate the big brown bat's range of adaptive behaviors that support target tracking in cluttered environments. 

Hearing mediates many behaviours critical for survival in echolocating bats, including foraging and navigation. Although most mammals are susceptible to progressive age-related hearing loss, the evolution of biosonar, which requires the ability to hear low-intensity echoes from outgoing sonar signals, may have selected against the development of hearing deficits in bats. Many echolocating bats exhibit exceptional longevity and rely on acoustic behaviours for survival to old age; however, relatively little is known about the ageing bat auditory system. In this study, we used DNA methylation to estimate the ages of wild-caught big brown bats (Eptesicus fuscus) and measured hearing sensitivity in young and ageing bats using auditory brainstem responses (ABRs) and distortion product otoacoustic emissions (DPOAEs). We found no evidence for hearing deficits in bats up to 12.5 years of age, demonstrated by comparable thresholds and similar ABR and DPOAE amplitudes across age groups. We additionally found no significant histological evidence for cochlear ageing, with similar hair cell counts, afferent and efferent innervation patterns in young and ageing bats. Here, we demonstrate that big brown bats show minimal evidence for age-related hearing loss and therefore represent informative models for investigating mechanisms that may preserve hearing function over a long lifetime. 

ABSTRACT Journal of Experimental Biology has a long history of reporting research discoveries on animal echolocation, the subject of this Centenary Review. Echolocating animals emit intense sound pulses and process echoes to localize objects in dynamic soundscapes. More than 1100 species of bats and 70 species of toothed whales rely on echolocation to operate in aerial and aquatic environments, respectively. The need to mitigate acoustic clutter and ambient noise is common to both aerial and aquatic echolocating animals, resulting in convergence of many echolocation features, such as directional sound emission and hearing, and decreased pulse intervals and sound intensity during target approach. The physics of sound transmission in air and underwater constrains the production, detection and localization of sonar signals, resulting in differences in response times to initiate prey interception by aerial and aquatic echolocating animals. Anti-predator behavioral responses of prey pursued by echolocating animals affect behavioral foraging strategies in air and underwater. For example, many insect prey can detect and react to bat echolocation sounds, whereas most fish and squid are unresponsive to toothed whale signals, but can instead sense water movements generated by an approaching predator. These differences have implications for how bats and toothed whales hunt using echolocation. Here, we consider the behaviors used by echolocating mammals to (1) track and intercept moving prey equipped with predator detectors, (2) interrogate dynamic sonar scenes and (3) exploit visual and passive acoustic stimuli. Similarities and differences in animal sonar behaviors underwater and in air point to open research questions that are ripe for exploration. 

A central aim of neuroethological research is to discover the mechanisms of natural behaviors in controlled laboratory studies. This goal, however, comes with challenges, namely the selection of experimental paradigms that allow full expression of natural behaviors. Here, we explore this problem in echolocating bats that evolved Doppler shift compensation (DSC) of sonar vocalizations to yield close matching between echo frequency and hearing sensitivity. We ask if behavioral tasks influence the precision of DSC in Pratt’s roundleaf bat, Hipposideros pratti , in three classic laboratory paradigms evoking audio-vocal adjustments: Stationary bats listening to echo playbacks, bats transported on a moving pendulum, and bats flying freely. We found that experimental conditions had a strong influence on the expression of the audiovocal frequency adjustments in bats. H. pratti exhibited robust DSC in both free-flying and moving-pendulum experiments but did not exhibit consistent audiovocal adjustments in echo playback experiments. H. pratti featured a maximum compensation magnitude of 87% and a compensation precision of 0.27% in the free flight experiment. Interestingly, in the moving pendulum experiment H. pratti displayed surprisingly high-precision DSC, with an 84% maximum compensation magnitude and a 0.27% compensation precision. Such DSC performance places H. pratti among the bat species exhibiting the most precise audio-vocal control of echo frequency. These data support the emerging view that Hipposiderid bats have a high-precision DSC system and highlight the importance of selecting experimental paradigms that yield the expression of robust natural behaviors. 

ABSTRACT Studies have shown that bats are capable of using visual information for a variety of purposes, including navigation and foraging, but the relative contributions of visual and auditory modalities in obstacle avoidance has yet to be fully investigated, particularly in laryngeal echolocating bats. A first step requires the characterization of behavioral responses to different combinations of sensory cues. Here, we quantified the behavioral responses of the insectivorous big brown bat, Eptesicus fuscus, in an obstacle avoidance task offering different combinations of auditory and visual cues. To do so, we utilized a new method that eliminates the confounds typically associated with testing bat vision and precludes auditory cues. We found that the presence of visual and auditory cues together enhances bats' avoidance response to obstacles compared with cues requiring either vision or audition alone. Analyses of flight and echolocation behaviors, such as speed and call rate, did not vary significantly under different obstacle conditions, and thus are not informative indicators of a bat's response to obstacle stimulus type. These findings advance the understanding of the relative importance of visual and auditory sensory modalities in guiding obstacle avoidance behaviors. 

Animals utilize a variety of active sensing mechanisms to perceive the world around them. Echolocating bats are an excellent model for the study of active auditory localization. The big brown bat ( Eptesicus fuscus ), for instance, employs active head roll movements during sonar prey tracking. The function of head rolls in sound source localization is not well understood. Here, we propose an echolocation model with multi-axis head rotation to investigate the effect of active head roll movements on sound localization performance. The model autonomously learns to align the bat’s head direction towards the target. We show that a model with active head roll movements better localizes targets than a model without head rolls. Furthermore, we demonstrate that active head rolls also reduce the time required for localization in elevation. Finally, our model offers key insights to sound localization cues used by echolocating bats employing active head movements during echolocation.