SUMMARYTemporary threshold shift (TTS) after loud noise exposure was investigated in a male and a female beluga whale (Delphinapterus leucas). The thresholds were evaluated using the evoked-potential technique, which allowed for threshold tracing with a resolution of ~1min. The fatiguing noise had a 0.5octave bandwidth, with center frequencies ranging from 11.2 to 90kHz, a level of 165dBre.1μPa and exposure durations from 1 to 30min. The effects of the noise were tested at probe frequencies ranging from -0.5 to +1.5octaves relative to the noise center frequency. The effect was estimated in terms of both immediate (1.5min) postexposure TTS and recovery duration. The highest TTS with the longest recovery duration was produced by noises of lower frequencies (11.2 and 22.5kHz) and appeared at a test frequency of +0.5octave. At higher noise frequencies (45 and 90kHz), the TTS decreased. The TTS effect gradually increased with prolonged exposures ranging from 1 to 30min. There was a considerable TTS difference between the two subjects.
Tone-tone masking was used to determine auditory brain-stem response tuning curves in dolphins (Tursiops truncatus) in a simultaneous-masking paradigm. The Q10 of the curves was as large as 16-19 in the frequency range 64-128 kHz. In the range 45-16 kHz, Q10 decreased proportionally to the frequency with the bandwidth of the curves being constant, about 3.5-4 kHz at the 10-dB level. Tuning curves below 45 kHz are supposed to reflect broad spectral bandwidth of the probe's effective part which is no longer than 0.5 ms, irrespective of actual probe duration. Tuning curves above 64 kHz are supposed to reflect the real frequency tuning of the dolphin's auditory system.
Notch-noise masking was used to measure frequency tuning in a dolphin (Tursiops truncatus) in a simultaneous-masking paradigm in conjunction with auditory brain-stem evoked potential recording. Measurements were made at probe frequencies of 64, 76, 90, and 108 kHz. The data were analyzed by fitting the rounded-exponent model of the auditory filters to the experimental data. The fitting parameter values corresponded to the filter tuning as follows: QER (center frequency divided by equivalent rectangular bandwidths) of 35 to 36.5 and Q10 dB of 18 to 19 at all tested frequencies.
In a bottlenose dolphin positions of sound receiving areas on the head surface were determined by comparing the acoustic delays from different sound-source positions. For this investigation, auditory brainstem responses (ABRs) to short tone pips were recorded and their latencies were measured at different sound source positions. After correction for the latency dependence on response amplitude, the difference in ABR latencies was adopted as being the difference of the acoustic delays. These delay differences were used to calculate the position of the sound-receiving point. Measurements were conducted at sound frequencies from 16 to 128 kHz, in half-octave steps. At probe frequencies of 16 and 22.5 kHz, the receiving area was located 21.7-26 cm caudal of the melon tip, which is near the bulla and auditory meatus. At higher probe frequencies, from 32 to 128 kHz, the receiving area was located from 9.3 to 13.1 cm caudal of the melon tip, which corresponds to a proximal part of the lower jaw. Thus, at least two sound-receiving areas (acoustic windows) with different frequency sensitivity were identified.
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