First published online March 30, 2006
Journal of Experimental Biology 209, 1430-1440 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02132
Wind generated by an attacking bat: anemometric measurements and detection by the praying mantis cercal system
Jeffrey D. Triblehorn* and
David D. Yager
Department of Psychology, University of Maryland, College Park, MD
20742, USA

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Fig. 1. (A) Schematic of the flight room setup for the physiological experiments,
viewed from above. The gray region represents the high-speed video-system's
calibrated area for distance measurements. The dark circle marks the location
of the mantis during the experiments. (B) Photo of a trial during the
anemometer measurements of bat-generated wind. The anemometer probe sits
inside the protective cage except for the sensor region positioned about 3 cm
outside the top of the cage. In the photo, the sensor sits 24 cm below the
mealworm target (inside circle) as the flying bat approaches the target just
before capturing it. The photo is from Camera 2 (A) of the high-speed video
system.
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Fig. 2. Implanted electrode recordings of wind-sensitive interneuron activity in
the abdominal connective of a mantis. (A) Neural activity from the mantis
recorded while blowing on the cerci (top) and just before the bat captured the
mantis (bottom). The similarity between the two responses indicates that both
traces result from wind-sensitive interneuron activity. Scale bars: 200 mV, 50
ms. (B) Same trial (shaded area in A) viewed on an expanded time scale. Scale
bars: 200 mV, 20 ms.
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Fig. 3. Five examples of abdominal connective activity recorded by an implanted
electrode during the last 280 ms before a flying, attacking bat captured the
mantis. Arrows mark the beginning of the response in each trial and the
numbers state the time (distance) that the response began before capture. The
examples illustrate that wind-related activity evoked by the bat's approach
was characterized by a sudden increase in neural activity that was sustained
until the bat captured the mantis. Scale bars: 100 mV, 25 ms.
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Fig. 4. Histograms of times (A) and distances (B) before capture when
wind-sensitive interneuron activity began during flying bat attacks.
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Fig. 5. Anemometer output from a single trial where the probe was placed 2 cm from
the mealworm target. Contact occurred as the wind velocity continued to
increase, but possibly before the wind velocity reached its peak. Scale bars:
50 cm s1, 50 ms.
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Fig. 6. Anemometer traces of wind generated by an attacking bat as it approaches a
mealworm target, captures it, and flies away. Since the anemometer was not
directly at the target's location, contact times (arrows) for each trace were
predicted based on the one trial when the anemometer was located at the target
(see Fig. 7). The examples
illustrate the major changes in the anemometer traces as peak velocities
increase; see text for details. The anemometer traces indicate that the bat
generates a short but strong stimulus as it approaches and captures the target
and a longer but weaker stimulus follows as the bat flies away. Scale bars: 50
cm s1, 500 ms.
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Fig. 7. (A) Peak wind velocities measured by the anemometer at distances
2060 cm from the target (N=94). The anemometer was within
1830 cm of the target in 77% of the trials. The shaded boxes indicate
the percentage of measured peak wind velocities that fell between 049,
5099 and >100 cm s1 for the data collected with
the anemometer within 2030 cm of the target only. (B) Distribution of
peak accelerations for 66 of the trials in A. Peak acceleration was calculated
using the onset time of the anemometer detecting the bat-generated wind to the
time of the peak velocity. (C) Comparison of peak velocity and peak
acceleration for each trial in B. For bat-generated wind, peak velocity and
peak acceleration were closely related, with peak acceleration increasing
exponentially with increasing peak velocity. The equation for the exponential
best fit line is
f(x)=4.980398x101*exp(4.814839x102*x).
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© The Company of Biologists Ltd 2006