First published online December 14, 2005
Journal of Experimental Biology 209, 152-157 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.01975
The absence of spatial echo suppression in the echolocating bats Megaderma lyra and Phyllostomus discolor
Maike Schuchmann,
Matthias Hübner and
Lutz Wiegrebe*
Department Biologie II, Universität München,
Großhadernerstrasse 2, 82152 Planegg-Martinsried, Germany

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Fig. 1. Characteristic samples of a Megaderma lyra echolocation call
(left) and a Phyllostomus discolor call (right). The upper panels
show the spectrograms (the shaded bar shows the magnitude in dB); the lower
panels show the oscillograms. M. lyra emits brief (0.5-1.5 ms),
broadband, multi-harmonic echolocation calls. The fundamental frequency is
frequency modulated from about 26 to 19 kHz. The strongest harmonics are the
3rd, 4th or 5th. P. discolor also emits brief (<3 ms), broadband,
multi-harmonic echolocation calls covering the frequency range between 40 and
90 kHz. The fundamental frequency is modulated from about 23.5 to 16 kHz.
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Fig. 2. Experimental designs for Megaderma lyra (A,B) and Phyllostomus
discolor (C). The layout consisted of a starting perch and two ultrasonic
speakers (ls), each of which was associated with a feeding dish (fd) next to
the speakers. The angle between the speakers in the M. lyra
experiments was 90°. This angle was positioned at an elevation of 45°
(B). A microphone (mic) was placed in front of the bat's head to pick up its
ultrasonic emissions. The P. discolor layout was a Y-shaped maze
(45x30 cm; wire mesh); the angle between the two legs was 45°. The
inner width of each leg was 10 cm.
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Fig. 3. Echo suppression in the echolocating bat Megaderma lyra. The
figure shows the percentage decisions towards the first of two reflections
plotted against the lead-lag delay. Chance performance is represented by the
horizontal broken line at 50%; significant performance is represented by the
dotted line at 75%. The bats' performance in the lead-only trials is shown by
the short horizontal lines. A-E show data for individuals; F shows the mean
performance of all bats. The two data plots in A,C,E show a first (solid line)
and second (broken line) data acquisition of these bats. Only one of five
M. lyra individuals spontaneously showed significant preference
(>75%) for the first of two reflections (C; first acquisition).
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Fig. 4. Echo suppression in the echolocating bat Phyllostomus discolor.
The figure shows the decision towards the first of two reflections plotted
against the lead-lag delay. Data are shown in the same format as in
Fig. 3. The two data plots
represent data from the two P. discolor individuals. None of these
showed significant spontaneous preference for the first of two
reflections.
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© The Company of Biologists Ltd 2006