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Spatial processing within the mustache bat echolocation system: possible mechanisms for optimization

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Summary

  1. 1.

    The directionality of an echolocation system is determined by the acoustic properties of both the emitter and receiver, i.e., by the radiation pattern of the emitted pulse and the directionally of the external ears. We measured the directionality of the echolocation system of the greater mustache bat (Pteronotus parnellii) at the 30 kHz, 60 kHz and 90 kHz harmonics of its echolocation pulse by summing, at points throughout the frontal sound field, the echo attenuation due to the spread of pulse energy and the attenuation due to the directionality of its external ears. The pulse radiation pattern at the 3 harmonics was measured by comparing the output of a microphone moved throughout the frontal sound field against a second reference microphone at the center of the field. External ear directionality at the 3 harmonics was measured by presenting free-field sounds throughout the frontal sound field, and recording the intensity thresholds of cochlear microphonic potentials, and the intensity thresholds of monaural neurons in the inferior colliculus tuned to one of the 3 harmonics.

  2. 2.

    When compared with ear directionality, the echolocation system was found to be more directional for the center of the sound field in several respects. At all harmonics, attenuation of sounds originating in the peripheral part of the field was increased by 10 to 13 dB. Areas of maximum sound intensity contracted toward the center of the field. Also, the isointensity contours of the echolocation system were more radially symmetrical about the center of the field.

  3. 3.

    At 60 kHz, sound intensity along the azimuth within the echolocation system was nearly constant 26° to either side of the center of the field. This suggests that the radiation pattern of the echolocation pulse and the directionality of the external ears complement one another to produce an acoustic environment at the center of the sound field in which stimulus intensity is stabilized to allow more effective analysis of various aspects of the echolocation target. In particular, we suggest that this intensity stabilization may allow the bat to more effectively resolve the interaural intensity differences it uses to localize prey.

  4. 4.

    Predictions of the azimuthal spatial tuning of binaurally sensitive neurons in the inferior colliculus within the echolocation system were compared with their spatial tuning when only ear directionality is considered. Within the echolocation system, neurons exhibited a sharper spatial tuning in that maximum responses were elicited over a more narrow azimuthal range, and responses decreased more rapidly outside of this range.

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Abbreviations

CF :

constant frequency

IID :

interaural intensity difference

References

  • Bell GP (1982) Behavioral and ecological aspects of gleaning by a desert insectivorous bat, Antrozous pallidus. Behav Ecol Sociobiol 6:217–233

    Google Scholar 

  • Blauert J (1969) Sound localization in the medial plane. Acustica 22:205–213

    Google Scholar 

  • Butler RA (1974) Does tonotopy subserve the perceived elevation of sound? Fed Proc 33:1920–1923

    Google Scholar 

  • Coles RB, Guppy A, Anderson ME, Schlegel P (1989) Frequency sensitivity and directional hearing in the gleaning bat, Plecotus auritus (Linnaeus 1758). J Comp Physiol A 165:269–280

    Google Scholar 

  • Fiedler J (1979) Prey catching with and without echolocation in the False Vampire (Megaderma lyra). Behav Ecol Sociobiol 6:155–160

    Google Scholar 

  • Fuzessery ZM (1986) Speculations on the role of frequency in sound localization Brain Behav Evol 28:95–108

    Google Scholar 

  • Fuzessery ZM, Pollak GD (1985) Determinants of sound location selectivity in bat inferior colliculus: A combined dichotic and free-field stimulation study. J Neurophysiol 54:757–781

    Google Scholar 

  • Fuzessery ZM, Wenstrup JJ, Pollak GD (1985) A representation of horizontal sound location in the inferior colliculus of the mustache bat (Pteronotus p. parnellii). Hearing Res 20:85–89

    Google Scholar 

  • Fuzessery ZM, Wenstrup JJ, Pollak GD (1990) Determinants of horizontal sound location selectivity of binaurally excited neurons in an isofrequency region of the mustache bat inferior colliculus. J Neurophysiol 63:1128–1147

    Google Scholar 

  • Goldman LJ, Henson OW (1977) Prey recognition and selection by the constant frequency bat, Pteronotus p. parnellii. Behav Ecol Sociobiol 2:411–419

    Google Scholar 

  • Grinnell AD, Grinnell VS (1965) Neural correlates of vertical sound localization by echolocating bats. J Physiol (Lond) 181:830–851

    Google Scholar 

  • Grinnell AD, Schnitzler H-U (1977) Directional sensitivity of echolocation in the horseshoe bat, Rhinolophus ferrumequinum. II. Behavioral directionality of hearing. J Comp Physiol 116:63–76

    Google Scholar 

  • Guppy A, Coles RB (1988) Acoustical and neural aspects of hearing in the Australian gleaning bats, Macroderma gigas and Nyctophilus gouldi. J Comp Physiol A 162:653–668

    Google Scholar 

  • Hartley DJ, Suthers RA (1987) The sound emission pattern and the acoustical role of the noseleaf in the echolocating bat, Carollia perspicillata. J Acoust Soc Am 82:1892–1900

    Google Scholar 

  • Hartley DJ, Suthers RA (1989) The emission pattern of the echolocating bat, Eptesicus fuscus. J Acoust Soc Am 85:1348–1351

    Google Scholar 

  • Hartley DJ, Suthers RA (1990) Sonar pulse radiation and filtering in the mustached bat, Pteronotus parnellii rubiginosus. J Acoust Soc Am 87:2756–2772

    Google Scholar 

  • Hartlidge H (1945) Avoidance of obstacles by bats. Nature 156:55

    Google Scholar 

  • Henson OW (1965) The activity and function of the middle ear muscles in echolocating bats. J Physiol (Lond) 180:871–887

    Google Scholar 

  • Henson OW, Bishop A, Keating A, Kobler J, Henson M, Wilson B, Hansen R (1987) Biosonar imaging of insects by Pteronotus p. parnellii, the mustache bat. Natl Geographic Res 3:82–101

    Google Scholar 

  • Kick SA, Simmons JA (1984) Automatic gain control in the bat's sonar receiver and the neuroethology of echolocation. J Neurosci 4:2725–2737

    Google Scholar 

  • Kobler JB, Wilson BS, Henson OW, Bishop AL (1985) Echo intensity compensation by echolocating bats. Hearing Res 20:99–108

    Google Scholar 

  • Lawrence BD, Simmons JA (1982) Measurements of atmospheric attenuation of ultrasonic frequencies and the significance for echolocation by bats. J Acoust Soc Am 71:585–590

    Google Scholar 

  • Marimuthu G, Neuweiler G (1987) The use of acoustical cues for prey detection by the Indian False Vampire Bat, Megaderma lyra. J Comp Physiol A 160:509–515

    Google Scholar 

  • Masters WM, Moffat AJM, Simmons JA (1985) Sonar tracking of horizontally moving targets by the big brown bat Eptesicus fuscus. Science 228:1331–1333

    Google Scholar 

  • Novick A (1963) Pulse duration in the echolocating bat, Pteronotus. Erg Biol 26:21–26

    Google Scholar 

  • Pollak GD, Henson OW, Johnson R (1979) Multiple specializations in the peripheral auditory system of the CF-FM bat, Pteronotus parnellii. J Comp Physiol 131:255–266

    Google Scholar 

  • Shimozawa T, Suga N, Hendler P, Schuetze S (1974) Directional sensitivity of echolocation system in bats producing frequency-modulated signals. J Exp Biol 60:53–69

    Google Scholar 

  • Simmons JA (1987) Directional hearing and sound localization in echolocating animals. In: Yost WA, Gourevitch G (eds) Directional hearing. Springer, New York, pp 214–225

    Google Scholar 

  • Suga N (1984) The extent to which biosonar information is represented in the bat auditory cortex. In: GM Edelman, WE Gall, WM Cowan (eds) Dynamic aspects of neocortical function. Wiley, New York, pp 315–374

    Google Scholar 

  • Suga N, Schlegel P (1972) Neural attenuation of responses to emitted sounds in echolocating bats. Science 177:82–84

    Google Scholar 

  • Tuttle MD, Ryan MJ (1981) Bat predation and the evolution of frog vocalizations in the neotropics. Science 214:677–678

    Google Scholar 

  • Webster FA (1967) Interception performance of echolocating bats in the presence of interference. In: Busnel RG (ed) Animal sonar systems. Lab Physiol Acoustique A, Juny-en-Josas, France, pp 673–713

    Google Scholar 

  • Wenstrup JJ, Fuzessery ZM, Pollak GD (1988) Binaural neurons in the mustache bat's inferior colliculus. II. Determinants of spatial responses among 60-kHz EI neurons. J Neurophysiol 60:1384–1404

    Google Scholar 

  • Zook JM, Winer JA, Pollak GD, Bodenhamer RD (1985) Topology of the central nucleus of the mustache bat's inferior colliculus: correlation of single unit properties and neuronal cytoarchitecture. J Comp Neurol 231:530–546

    Google Scholar 

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Fuzessery, Z.M., Hartley, D.J. & Wenstrup, J.J. Spatial processing within the mustache bat echolocation system: possible mechanisms for optimization. J Comp Physiol A 170, 57–71 (1992). https://doi.org/10.1007/BF00190401

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