First published online August 4, 2005
Journal of Experimental Biology 208, 3121-3131 (2005)
Published by The Company of Biologists 2005
doi: 10.1242/jeb.01742
Ontogenetic changes in the response properties of individual, primary auditory afferents in the vocal plainfin midshipman fish Porichthys notatus Girard
Joseph A. Sisneros1,2,* and
Andrew H. Bass1
1 Department of Neurobiology and Behavior, Cornell University, Ithaca, NY
14853, USA
2 Department of Psychology, University of Washington, Seattle, WA 98195,
USA

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Fig. 1. Dorsal view of midshipman brain and inner ear. Small arrow marks the area
of the VIIIs nerve innervating the saccule where recordings were
made. C, cerebrum; M, midbrain; T, telencephalon.
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Fig. 2. Resting discharge rate histogram of auditory saccular afferent neurons
recorded from juvenile and adult midshipman fish (P. notatus). The
numbers of animals and auditory saccular afferent neurons tested are
indicated, respectively, in parentheses.
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Fig. 3. Relationship of resting discharge rate of auditory saccular afferent
neurons with standard length (SL) recorded from juvenile and adult
midshipman fish. Note that resting discharge rate increases with SL.
Values are means ± S.E.M. for each
animal.
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Fig. 4. Iso-intensity response curves for the entire population of juvenile and
adult midshipman auditory saccular afferent neurons to 130 dB (re 1 µPa)
iso-intensity tones. The numbers of animals and auditory saccular afferent
neurons tested are indicated, respectively, in parentheses. Iso-intensity
curves based on vector strength (VS) of synchronization show VS values for
each frequency tested in terms of the median (black filled symbols), 25th
percentile (bottom bar) and 75th percentile (top bar).
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Fig. 5 Best frequency histogram of auditory saccular afferent neurons recorded
from juvenile and adult midshipman fish (P. notatus). The
distribution of best frequencies (BFs) for auditory saccular afferents is
based on the vector strength of synchronization to iso-intensity tones of 130
dB (re 1 µPa). The numbers of animals and auditory saccular afferent
neurons tested are indicated, respectively, in parentheses.
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Fig. 6. Relationship of auditory threshold (decibels, re 1 µPa) at best
frequency (BF) of auditory saccular afferent neurons with standard length
(SL) recorded from juvenile and adult midshipman fish. Note that
threshold at BF decreases with SL.
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Fig. 7. Relationship of vector strength of synchronization at best frequency (BF)
with resting discharge rate of auditory saccular afferent neurons recorded
from juvenile and adult midshipman fish.
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Fig. 8. (A) Representative example of a single grunt recorded at 16°C from a
nesting type I male midshipman fish. Bar, 10 ms. (B) Comparison of the power
spectrum of the representative grunt shown in A (grey trace) and the frequency
sensitivity of auditory saccular afferent neurons recorded from juvenile
(small and large) and adult (non-reproductive and reproductive) midshipman
fish. (C) Representative example of a growl recorded at 16°C from a
nesting type I male midshipman fish. Bar, 500 ms. (D) Comparison of the power
spectrum of the representative growl in C (grey trace) and the frequency
sensitivity of auditory saccular afferent neurons recorded from juvenile
(small and large) and adult (non-reproductive and reproductive) midshipman
fish. (E) Representative example of a hum recorded at 16°C from a nesting
type I male midshipman fish. Bar, 10 ms. (F) Comparison of the power spectrum
of the representative hum in E (grey trace) and the frequency sensitivity of
auditory saccular afferent neurons recorded from juvenile (small and large)
and adult (non-reproductive and reproductive) midshipman fish. Iso-intensity
response curves are based on vector strength (VS) of synchronization to
iso-intensity tones of 130 dB (re 1 µPa) and show median VS values for
juvenile and adult midshipman (filled circles, squares and triangles from
Fig. 4; open triangle,
non-reproductive female midshipman fish from
Sisneros and Bass, 2003 ).
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© The Company of Biologists Ltd 2005