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      The resting frequency of echolocation signals changes with body temperature in the hipposiderid bat Hipposideros armiger

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          ABSTRACT

          Doppler shift (DS) compensating bats adjust in flight the second harmonic of the constant-frequency component (CF 2) of their echolocation signals so that the frequency of the Doppler-shifted echoes returning from ahead is kept constant with high precision (0.1–0.2%) at the so-called reference frequency ( f ref). This feedback adjustment is mediated by an audio–vocal control system that correlates with a maximal activation of the foveal resonance area in the cochlea. Stationary bats adjust the average CF 2 with similar precision at the resting frequency ( f rest), which is slightly below the f ref. Over a range of time periods (from minutes up to years), variations of the coupled f ref and f rest have been observed, and were attributed to age, social influences and behavioural situations in rhinolophids and hipposiderids, and to body temperature effects and flight activity in Pteronotus parnellii. We assume that, for all DS-compensating bats, a change in body temperature has a strong effect on the activation state of the foveal resonance area in the cochlea, which leads to a concomitant change in emission frequency. We tested our hypothesis in a hipposiderid bat, Hipposideros armiger, and measured how the circadian variation of body temperature at activation phases affected f rest. With a miniature temperature logger, we recorded the skin temperature on the back of the bats simultaneously with echolocation signals produced. During warm-up from torpor, strong temperature increases were accompanied by an increase in f rest, of up to 1.44 kHz. We discuss the implications of our results for the organization and function of the audio–vocal control systems of all DS-compensating bats.

          Abstract

          Summary: In Hipposideros armiger, the variation of body temperature during activation phases results in a concomitant change in emission frequency.

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          Most cited references63

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          The evolution of echolocation in bats.

          Recent molecular phylogenies have changed our perspective on the evolution of echolocation in bats. These phylogenies suggest that certain bats with sophisticated echolocation (e.g. horseshoe bats) share a common ancestry with non-echolocating bats (e.g. Old World fruit bats). One interpretation of these trees presumes that laryngeal echolocation (calls produced in the larynx) probably evolved in the ancestor of all extant bats. Echolocation might have subsequently been lost in Old World fruit bats, only to evolve secondarily (by tongue clicking) in this family. Remarkable acoustic features such as Doppler shift compensation, whispering echolocation and nasal emission of sound each show multiple convergent origins in bats. The extensive adaptive radiation in echolocation call design is shaped largely by ecology, showing how perceptual challenges imposed by the environment can often override phylogenetic constraints.
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            Cochlear outer hair cell motility.

            Normal hearing depends on sound amplification within the mammalian cochlea. The amplification, without which the auditory system is effectively deaf, can be traced to the correct functioning of a group of motile sensory hair cells, the outer hair cells of the cochlea. Acting like motor cells, outer hair cells produce forces that are driven by graded changes in membrane potential. The forces depend on the presence of a motor protein in the lateral membrane of the cells. This protein, known as prestin, is a member of a transporter superfamily SLC26. The functional and structural properties of prestin are described in this review. Whether outer hair cell motility might account for sound amplification at all frequencies is also a critical question and is reviewed here.
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              Die Ultraschall-Ortungslaute der Hufeisen-Flederm�use (Chiroptera-Rhinolophidae) in verschiedenen Orientierungssituationen

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                Author and article information

                Journal
                J Exp Biol
                J Exp Biol
                JEB
                jexbio
                The Journal of Experimental Biology
                The Company of Biologists Ltd
                0022-0949
                1477-9145
                1 February 2022
                3 February 2022
                3 February 2022
                : 225
                : 3
                : jeb243569
                Affiliations
                Animal Physiology, Institute for Neurobiology, Faculty of Science, University of Tübingen , 72076 Tübingen, Germany
                Author notes
                [* ]Author for correspondence ( diana.schoeppler@ 123456uni-tuebingen.de )
                Author information
                http://orcid.org/0000-0002-6712-7036
                Article
                JEB243569
                10.1242/jeb.243569
                8918815
                34989397
                9c13171c-7a3e-4572-8ef8-c5e5bdf6b407
                © 2022. Published by The Company of Biologists Ltd

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.

                History
                : 17 September 2021
                : 26 December 2021
                Funding
                Funded by: Werner Reichardt Centre for Integrative Neuroscience;
                Funded by: University of Tübingen, http://dx.doi.org/10.13039/501100002345;
                Categories
                Research Article

                Molecular biology
                audio–vocal feedback control,auditory fovea,cf-fm echolocation signals,doppler shift compensation,flutter detection

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