JN Fuel your research with LabChart
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 90: 2274-2290, 2003; doi:10.1152/jn.00101.2003
0022-3077/03 $5.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in ISI Web of Science
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via ISI Web of Science (8)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vater, M.
Right arrow Articles by Russell, I. J.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vater, M.
Right arrow Articles by Russell, I. J.

Development of Echolocation Calls in the Mustached Bat, Pteronotus parnellii

M. Vater1, M. Kössl2, E. Foeller2, F. Coro3, E. Mora3 and I. J. Russell4

1 Institute of Biochemistry and Biology, University of Potsdam, 14471 Potsdam; 2 Zoological Institute, University of Frankfurt, 60323 Frankfurt am Main, Germany; 3 Department of Animal Physiology, University of Habana, Calle 25 #455, Vedado, La Habana, Cuba; 4 School of Biology, University of Sussex, Falmer, Brighton BN19QG, United Kingdom

Submitted 3 February 2003; accepted in final form 18 June 2003

Adult mustached bats employ Doppler-sensitive sonar to hunt fluttering prey insects in acoustically cluttered habitats. The echolocation call consists of 4–5 harmonics, each composed of a long constant frequency (CF) component flanked by brief frequency modulations (FM). The 2nd harmonic CF component (CF2) at 61 kHz is the most intense, and analyzed by an exceptionally sharply tuned auditory system. The maturation of echolocation calls and the development of Doppler-shift compensation was studied in Cuba where large maternity colonies are found in hot caves. In the 1st postnatal week, infant bats did not echolocate spontaneously but could be induced to vocalize CF-FM signals by passive body motion. The CF2 frequency emitted by the smallest specimens was at 48 kHz (i.e., 0.4 octaves lower than the adult signal). CF-FM signals were spontaneously produced in the 2nd postnatal week at a CF2 frequency of 52 kHz. The CF2 frequencies of induced and spontaneous calls shifted upward to reach a value of 60.5 kHz in the 5th postnatal week. Standard deviations of CF2 frequency were large (up to ±1.5 kHz) in the youngest bats and dropped to values of ±250 Hz at the end of the 3rd postnatal week. Some individuals in the 4th and 5th postnatal weeks emitted with adultlike frequency precision of about ±100 Hz. In the youngest bats, the 1st harmonic CF component (CF1) was up to 22 dB stronger than CF2. Adultlike relative levels of CF1 (–28 dB relative to CF2) were reached in the 5th postnatal week. In spontaneously emitted CF-FM calls, the duration of the CF2 component gradually increased with age from 5 ms to maximum values of 18 ms. Durations of the CF2 component in induced calls averaged 7 ± 2.6 ms in the 1st postnatal week and 8.2 ± 1.5 ms in the 5th postnatal week. There were no age-related changes in duration of the terminal FM sweep (3 ± 0.4 ms) in both induced and spontaneous calls. The magnitude of the terminal FM sweep in spontaneous calls was not correlated with age (mean 13.5 ± 2 kHz). Values for induced calls slightly increased with age from 11 ± 2 to 13 ± 2 kHz. The emission rate of induced CF-FM signals increased with age from values of 2.5 ± 2 to 17 ± 5 pulses/s. Values for spontaneously emitted calls were 4.4 ± 3 and 9 ± 4.5 pulses/s, respectively. Doppler-shift compensation, as tested in the pendulum task, emerged during the 4th postnatal week in young bats that were capable of very brief active flights, but before the time of active foraging outside the cave.


Address for reprint requests and other correspondence: M. Vater, Institute of Biochemistry and Biology, University of Potsdam, Lennestr. 7a 14471 Potsdam, Germany (E-mail: vater{at}rz.uni-potsdam.de).




This article has been cited by other articles:


Home page
J. Exp. Biol.Home page
D. M. Caspary, L. Ling, J. G. Turner, and L. F. Hughes
Inhibitory neurotransmission, plasticity and aging in the mammalian central auditory system
J. Exp. Biol., June 1, 2008; 211(11): 1781 - 1791.
[Abstract] [Full Text] [PDF]


Home page
J. Neurosci.Home page
I. J. Russell, M. Drexl, E. Foeller, M. Vater, and M. Kossl
The Development of a Single Frequency Place in the Mammalian Cochlea: The Cochlear Resonance in the Mustached Bat Pteronotus parnellii
J. Neurosci., November 26, 2003; 23(34): 10971 - 10981.
[Abstract] [Full Text] [PDF]


Home page
J. Neurophysiol.Home page
M. Kossl, E. Foeller, M. Drexl, M. Vater, E. Mora, F. Coro, and I. J. Russell
Postnatal Development of Cochlear Function in the Mustached Bat, Pteronotus parnellii
J Neurophysiol, October 1, 2003; 90(4): 2261 - 2273.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2003 by the The American Physiological Society.