First published online November 4, 2005
Journal of Experimental Biology 208, 4213-4222 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01896
Response properties of electrosensory afferent fibers and secondary brain stem neurons in the paddlefish
Michael H. Hofmann1,*,
Boris Chagnaud1 and
Lon A. Wilkens2
1 University of Bonn, Institute of Zoology, Poppelsdorfer Schloss, 53115
Bonn, Germany
2 Center for Neurodynamics, Department of Biology, University of Missouri-St
Louis, MO 63121, USA

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Fig. 1. Responses of a DON neuron to a 2 Hz sinuosidal electric field moved at 0.5
cm s-1 along the rostro-caudal axis of the rostrum. (A) Firing rate
as a function of time. (B) As in A, but filtered and multiplied by the 2
Hzstimulus, showing the phase relationship of the response to the
stimulus.
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Fig. 2. Autocorrelation [C(n)] analysis of a primary afferent (PA) fiber
(A) and a dorsal octavolateral nucleus (DON) unit (B). Solid lines, original
data; dotted lines, shuffled data. Only the PA shows long-range
autocorrelation. (C) Autocorrelation index of 30 PA fibers and 60 DON units
plotted against the mean firing rate. Note the lack of higher autocorrelation
values in DON units.
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Fig. 3. Peak firing rate of primary afferent (PA) fibers (A) and dorsal
octavolateral nucleus (DON) units (B) during stimulation with sinusoidal
electric fields of different frequency. The response magnitudes at each
stimulus frequency are similar and the overall frequency tuning curves are not
different between PA fibers and DON units.
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Fig. 4. Phase plots of the responses of 15 primary afferent (PA) fibers (A) and 15
dorsal octavolateral nucleus (DON) units (B) during stimulation with a small
dipole field moved slowly along the rostro-caudal axis of the rostrum. Traces
are sorted by the location of the receptive field. Stimulus frequency was 2 Hz
and the speed 0.5 cm s-1. Stimulus electrodes were oriented
perpendicular to movement direction.
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Fig. 5. Firing rates as a function of time for nine primary afferent (PA) fibers
(A) and nine dorsal octavolateral nucleus (DON) units (B) during stimulation
with a moving DC field (top nine traces); the lowest trace in each panel is
the average. Traces are aligned by the receptive field position to allow
averaging. The x-axis zero point marks the center of the receptive
field. The speed of the DC stimulus was 5 cm s-1. Response
amplitude and shape were similar for PA fibers and DON units.
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Fig. 6. x-y plots of receptive field position of dorsal octavolateral
nucleus (DON) units vs cell location within the DON. The
y-axis represents the normalized receptive field position. Zero is at
the tip of the rostrum and 10 cm is the position of the nose opening just in
front of the eye. Receptive field values for different sized fish were
normalized and projected onto a standard fish with a tip-to-nose distance of
10 cm. (A) The x-axis represents the position of the cell along the
rostro-caudal axis as % of total DON length. Zero represents the rostral end
of the DON, 100 represents the caudal end of the DON. (B) The x-axis
gives the cell position along the medio-lateral extent of the DON in percent.
Zero means the medial border of the DON, 100 its lateral edge. Each symbol
represents a DON unit whose receptive field position was measured. There is no
correlation between the location of a cell in the DON and its receptive field
along the rostro-caudal axis of the rostrum.
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© The Company of Biologists Ltd 2005