First published online December 1, 2006
Journal of Experimental Biology 209, 4994-5004 (2006)
Published by The Company of Biologists 2006
doi: 10.1242/jeb.02609
Acoustic communication in territorial butterflyfish: test of the sound production hypothesis
Timothy C. Tricas*,
Stephen M. Kajiura
and
Randall K. Kosaki
Department of Zoology and Hawaii Institute of Marine Biology,
University of Hawaii at Manoa, Honolulu, HI 96822, USA

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Fig. 1. Schematic diagram of the laterophysic system in butterflyfishes of the
genus Chaetodon. This unique anatomical feature is a putative
acoustico-lateralis hearing mechanism located at the junction of the trunk
lateral line (TLL) and head lateral line (HLL) canal systems. The laterophysic
connection is formed by gas-filled horns (H) that extend from the anterior
swim bladder (SB) and a small tympanum (dark circle and X) on the medial edge
of the canal in the supracleithrum bone (S). The swim bladder horns also
project towards the otic capsule. Figure modified with permission from Webb
and Smith (2000 ).
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Fig. 2. Model bottle method used in field experiments to evoke and record motor and
acoustic behaviors produced by Chaetodon multicinctus. One or two
fish (one shown) were collected by divers, placed in a glass jar and
introduced into the territory of a conspecific pair. A hydrophone (H) placed
near the bottle detected sounds that were recorded on the audio channel of an
underwater video camera (VC). The resident pair quickly discovered the
intruders and initiated agonistic acoustic behaviors.
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Fig. 3. Behaviors associated with sound production in the multibanded
butterflyfish, Chaetodon multicinctus. (A) The tail slap behavior
occurs after escalated displays and aggression by territorial residents
towards bottled intruders and is performed within a distance of one body
length from the bottle. The tail slap produces both a low frequency
hydrodynamic pulse and a brief broadband acoustic click. (B) The jump behavior
is displayed by resident fish and involves several movement patterns: the
approach and face (1) and rapid turn (2) are followed by a short swimming
ascent (3) and intense lateral display (4). The rapid turn produces a low
frequency hydrodynamic pulse that is followed by several rapid acoustic
pulses. (C) The pelvic fin flick behavior is produced by both residents and
bottled intruders (illustrated), involves the extension of the pelvic fins and
a single acoustic pulse. (D) The grunt train sound was produced only by
bottled fish when approached by territory residents and may be an alert call
to the mate. No body movements were observed during the production of this
sound. Broken lines indicate sound production.
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Fig. 4. Motor patterns and sounds produced by multiband butterflyfish,
Chaetodon multicinctus during agonistic interactions with bottled
conspecifics. (A) The tail slap starts with a lateral display followed by tail
slap and turn motor patterns (lower panel) that produce acoustic stimuli
(waveform on lower trace). A strong hydrodynamic pulse with signals at 20-60
Hz results from the lateral motion of the body towards the intruder (lower
spectrogram). The tail slap occurs at the end of the turn that produces a
broadband click (upper spectrogram). In this instance the tail slap was
immediately followed by a second lateral display. (B) Jump behavior starts
with a frontal motor display towards the bottled intruders, a rapid turn of
the body, and swimming ascent that is followed by an intense lateral display
(lower panel). The turn and ascend behaviors produce acoustic stimuli that
include a low frequency component made during the turn followed by a pulse
train during the ascent (waveform on lower trace). Note that spectrum of
sounds made during both the turn and ascent are from <100-700 Hz, with
lower frequencies due to the hydrodynamic pulse made during the turn
(spectrogram).
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Fig. 5. Relative frequency of sounds produced during aggressive social interactions
in the multiband butterflyfish, Chaetodon multicinctus. The tail
slap, grunt and dorsal-anal fin (DA) erect acoustic behaviors were produced
exclusively by territory residents and directed towards bottled conspecifics.
Grunt trains were recorded only from bottled fish (most frequently when in
pairs) when territory holders came into view and may be an alert or distress
signal to the mate. The fin flick acoustic pulse was produced by both resident
and bottled fish during confrontations. N values are given beneath
each behavior.
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Fig. 6. Sound production by multiband butterflyfish, Chaetodon
multicinctus, intruders during encounters with conspecific territory
holders. (A) The pelvic flick behavior by an intruder involves the extension
of the pelvic fins that produces an acoustic stimulus during this motion
(waveform on lower trace). This sound has a frequency spectrum just below 200
Hz and is also produced during displays by resident fish towards bottled
intruders. Arrows show start and end of pelvic fin extension. (B) The grunt
train sound is produced by bottled intruder pairs when confronted by territory
residents. Unlike all other acoustic signals observed, the grunt train was not
associated with any visible body movements, thus most likely is caused by
internal muscle movements. This sound included a series of regular spaced
pulses (waveform on lower trace) that have a strong frequency component at
400-500 Hz (spectrogram). Note the harmonics associated with each pulse that
indicate that this internally generated sound may result in part from
resonance of the swim bladder.
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© The Company of Biologists Ltd 2006