First published online September 9, 2005
Journal of Experimental Biology 208, 3441-3450 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01766
Sensitivity of the anterior lateral line to natural stimuli in the oyster toadfish, Opsanus tau (Linnaeus)
Lucy M. Palmer1,2,
Max Deffenbaugh2,3 and
Allen F. Mensinger1,2,*
1 Biology Department, University of Minnesota Duluth, Duluth, MN 55812,
USA
2 Marine Biological Laboratory, Woods Hole, MA 02543, USA
3 ExxonMobil Upstream Research Company, PO Box 2189, Houston, TX 77252,
USA

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Fig. 1. Dorsal view of the experimental arena. The recharging habitat and stage
(RECHABS) consists of the cylindrical habitat (H) and octagonal stage (S).
Neural telemetry and tag recharging could transpire when the fish was in the
habitat or over the stage. The black circle (arrow) represents an opaque
barricade that restricted the prey and the toadfish to the stage area. Fish
movements were recorded with an overhead video camera (C). Drawing is not to
scale.
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Fig. 2. The mean normalized neural firing rates of (A) silent (N=4) and
(B) spontaneously active afferent fibers (N=5) of the anterior
lateral line are plotted versus the distance of the innervated
neuromasts to the prey. All firing rates were normalized according to the
maximum firing rate recorded during each trial. Neural activity was analyzed
only when the prey fish was at the same location for greater than 500 ms. All
distances were measured from the insertion point of the nearside prey pectoral
fin to the neuromast that was innervated by the recording. Asterisks indicate
significantly different means from controls (ANOVA). The broken horizontal
line in B represents the mean normalized spontaneous firing rate from
spontaneously active fibers.
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Fig. 3. The probability of a silent fiber (triangles) firing during a prey
encounter and the probability of a spontaneously active fiber increasing its
discharge rate one (filled circle) or two (open circle) standard deviations
above its spontaneous discharge rate during a prey encounter is plotted
versus prey distance. If the silent fiber fired during the event, it
was considered stimulated, and the probability of the silent fibers firing was
calculated as: (stimulated encounters/total encounters)x100. If the
firing activity of the spontaneously active fibers firing increased one and/or
two standard deviations above its mean resting discharge rate it was
considered stimulated and the probability was calculated as: (stimulated
encounters >1 S.D./total encounters)x100 and
(stimulated encounters >2 S.D./total
encounters)x100. The data represent the summary of all trials for each
fiber class, and each point represents a minimum of 15 trials at each
distance. Prey distance was binned into 2 cm segments.
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Fig. 4. The activity of a silent, afferent fiber innervating a superficial
neuromast on the infraorbital lateral line, as monitored during prey movement.
(A) The distance (cm) of the prey fish from the recorded neuromast. (B) The
full neural waveform from the anterior lateral line nerve that was transmitted
via inductive telemetry. Although multiunit activity is visible in
the trace, only the fiber with the greatest amplitude of action potential was
used for data analysis. The fiber had no spontaneous activity and exhibited
maximum firing ( 10 Hz) when the prey fish was within 1 cm of the
neuromast.
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Fig. 5. Neural activity during the approach of a single prey fish. The diagram
depicts the head of the toadfish projecting out of its habitat and the
sequential positions of the approaching prey: (A) 10 cm; (B) 3.5 cm; (C) 1.0
cm. Images were reconstructed from single video frames. The letter next to the
prey fish corresponds to neural activity from a superficial neuromast on the
suborbital portion of the infraorbital lateral line. Although multiunit
activity is visible in the trace, data analysis was restricted to the fiber
with the greatest amplitude of action potential.
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Fig. 6. Firing rates of (A) a spontaneously active afferent fiber and (B) a silent
fiber in response to a prey fish located at variable distances from the
neuromast. Both fibers innervated superficial neuromasts. All distances were
measured from the insertion point of the nearside prey pectoral fin to the
neuromast that was innervated by the recording. The broken horizontal line in
A represents the mean spontaneous activity. All firing rates were normalized
according to the maximum firing rate elicited by prey movements during each
trial. Neural activity was analyzed only when the prey fish was at the same
location for greater than 500 ms.
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Fig. 7. Mean firing rate (± 1 S.E.M.) of
four anterior lateral line afferents fibers [three spontaneous (SP) and one
silent (SL)] immediately before (open) and during (filled) a toadfish prey
strike. Numbers above the bars represent the number of prey strikes that were
averaged for each fiber.
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Fig. 8. Neural activity from an afferent anterior lateral line fiber before, during
and after a prey strike. Vertical lines on the trace indicate individual
action potentials from a single fiber that were discriminated based on spike
amplitude. The arrows indicate initiation of opercular contraction for each
ventilation cycle. The time during the strike, capture and subsequent
expulsion of the prey is boxed in A, and this interval is expanded in B. The
prey was retained in the mouth of the toadfish for approximately 1 s before
being expelled.
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Fig. 9. The picture shows the water movements produced by an 8 cm SL Fundulus
heteroclitus taken with a digital video camera at 1000x1000 pixel
resolution. Each velocity vector represents the average of a 32 pixelx32
pixel window, and the center of each window is spaced 16 pixels apart.
Velocities are presented by pseudo color images. Scale bar, 2 cm.
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Fig. 10. The frequency of attacks by 8 cm SL toadfish at 2 cm SL guppies is plotted
versus the distance between the two fish at the time the toadfish
launched its attack. The total number of attacks analyzed was 78. Modified
from Price and Mensinger
(1999 ).
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© The Company of Biologists Ltd 2005