Hearing Sensitivity to Gliding Rippled Spectra in Hearing-Impaired Listeners.

Objectives: Sensitivity to the gliding of ripples in rippled-spectrum signals was measured in both normal-hearing and hearing-impaired listeners.

Methods: The test signal was a 2 oct wide rippled noise centered at 2 kHz, with the ripples gliding downward along the frequency scale. Both the gliding velocity and ripple density were frequency-proportional across the signal band.

Monaural and dichotic forward masking in the dolphin's auditory system.

Short-latency auditory-evoked potentials (AEPs) were recorded non-invasively in the bottlenose dolphin Tursiops truncatus. The stimuli were two sound clicks that were played either monaurally (both clicks to one and the same acoustic window) or dichotically (the leading stimulus (masker) to one acoustic window and the delayed stimulus (test) to the other window). The ratio of the levels of the two stimuli was 0, 10, or 20 dB (at 10 and 20 dB, the leading stimulus was of a higher level).

Forward masking in a bottlenose dolphin Tursiops truncatus: dependence on azimuthal positions of the masker and test sources.

Forward masking was investigated by the auditory evoked potentials (AEP) method in a bottlenose dolphin Tursiops truncatus using stimulation by two successive acoustic pulses (the masker and test) projected from spatially separated sources. The positions of the two sound sources either coincided with or were symmetrical relative to the head axis at azimuths from 0 to ± 90°. AEPs were recorded either from the vertex or from the lateral head surface next to the auditory meatus.

Ripple density resolution dependence on ripple width.

The goal of the study was to investigate how variations in ripple width influence the ripple density resolution. The influence of the ripple width was investigated with two experimental paradigms: (i) discrimination between a rippled test signal and a rippled reference signal with opposite ripple phases and (ii) discrimination between a rippled test signal and a flat reference signal. The ripple density resolution depended on the ripple width: the narrower the width, the higher the resolution.

The rate of cochlear compression in a dolphin: a forward-masking evoked-potential study.

The "active" cochlear mechanism of hearing manifests in the cochlear compression. Investigations of compression in odontocetes help to determine the frequency limit of the active mechanism. The compression may be evaluated by comparison of low- and on-frequency masking.

Rippled-spectrum resolution dependence on frequency: Estimates obtained by discrimination from rippled and nonrippled reference signals.

The resolution of spectral ripples is a useful test for the spectral resolution of hearing. However, the use of different measurement paradigms might yield diverging results because of a paradigm-dependent contribution of excitation-pattern and temporal-processing mechanisms. In the present study, ripple-density resolution was measured in normal-hearing listeners for several frequency bands (centered at 0.

Level-dependent masking of the auditory evoked responses in a dolphin: manifestation of the compressive nonlinearity.

At suprathreshold sound levels, interactions between masking noise and sound signals are liable to compressive nonlinearity in the auditory system. The compressive nonlinearity is a property of the "active" cochlear mechanism. It is not known whether this mechanism is capable to function at frequencies close to or above 100 kHz that are available to odontocetes (toothed whales, dolphins, and porpoises).

Estimates of Ripple-Density Resolution Based on the Discrimination From Rippled and Nonrippled Reference Signals.

Rippled-spectrum stimuli are used to evaluate the resolution of the spectro-temporal structure of sounds. Measurements of spectrum-pattern resolution imply the discrimination between the test and reference stimuli. Therefore, estimates of rippled-pattern resolution could depend on both the test stimulus and the reference stimulus type.

Adaptation processes in the auditory system of a beluga whale Delphinapterus leucas.

The effects of prolonged sound stimuli (tone pip trains) on evoked potentials (the rate following response, RFR) were investigated in a beluga whale. The stimuli (rhythmic tone pips) were of 64 kHz frequency at levels from 80 to 140 dB re 1 μPa. During stimulation, every 1000 ms stimulus level either was kept constant (the steady-state stimulation) or changed up/down by 20 or 40 dB.

Contribution of Cochlear Compression to Discrimination of Rippled Spectra in On- and Low-frequency Noise.

The goal of the study was to assess cochlear compression when rippled-spectrum signals are perceived in noise assuming that the noise might produce both masking and confounding effects. In normal listeners, discrimination between rippled signals with and without ripple phase reversals was assessed in background noise. The signals were band-limited (0.

Hearing sensitivity to gliding rippled spectrum patterns.

The sensitivity of human hearing to gliding rippled spectrum patterns of sound was investigated. The test signal was 2-oct wide rippled noise with the ripples gliding along the frequency scale. Both ripple density and gliding velocity were frequency-proportional across the signal band; i.

Discrimination of rippled-spectrum patterns in noise: A manifestation of compressive nonlinearity.

In normal-hearing listeners, rippled-spectrum discrimination was psychophysically investigated in both silence and with a simultaneous masker background using the following two paradigms: measuring the ripple density resolution with the phase-reversal test and measuring the ripple-shift threshold with the ripple-shift test. The 0.5-oct wide signal was centered on 2 kHz, the signal levels were 50 and 80 dB SPL, and the masker levels varied from 30 to 100 dB SPL.

Auditory sensitivity to local stimulation of the head surface in a beluga whale (Delphinapterus leucas).

Using the auditory evoked response technique, sensitivity to local acoustic stimulation of the ventro-lateral head surface was investigated in a beluga whale (Delphinapterus leucas). The stimuli were tone pip trains of carrier frequencies ranging from 16 to 128 kHz with a pip rate of 1 kHz. For higher frequencies (90-128 kHz), the low-threshold point was located next to the medial side of the middle portion of the lower jaw.

Auditory evoked potentials in the auditory system of a beluga whale Delphinapterus leucas to prolonged sound stimuli.

The effects of prolonged (up to 1500 s) sound stimuli (tone pip trains) on evoked potentials (the rate following response, RFR) were investigated in a beluga whale. The stimuli (rhythmic tone pips) were of frequencies of 45, 64, and 90 kHz at levels from 20 to 60 dB above threshold. Two experimental protocols were used: short- and long-duration.

Frequency Tuning of Hearing in the Beluga Whale.

Data on frequency tuning in odontocetes are contradictory: different authors have reported filter qualities from 2 to almost 50. In this study, frequency tuning was measured in a beluga whale (Delphinapterus leucas) using a rippled-noise test stimulus in conjunction with the auditory evoked potential (AEP) technique. The response to ripple reversions was considered to indicate resolvability of the ripple pattern.

Is Sound Exposure Level a Convenient Metric to Characterize Fatiguing Sounds? A Study in Beluga Whales.

Both the level and duration of fatiguing sounds influence temporary threshold shifts (TTSs) in odontocetes. These two parameters were combined into a sound exposure level (SEL). In the beluga whale Delphinapterus leucas, TTSs were investigated at various sound pressure level (SPL)-to-duration ratios at a specific SEL.

Temporary Threshold Shifts in Naïve and Experienced Belugas: Can Dampening of the Effects of Fatiguing Sounds Be Learned?

In belugas (Delphinapterus leucas), substantial (10-15 dB) differences in temporary threshold shifts (TTSs) were observed between the first and subsequent experimental sessions in the same subjects. In the first session (naïve subject state), the TTSs produced by exposure to fatiguing noises were larger than the TTSs produced in subsequent sessions (experienced subject state). After one to two sessions, the TTSs stabilized.

Hearing Sensitivity to Shifts of Rippled-Spectrum Sound Signals in Masking Noise.

The goal of the study was to enlarge knowledge of discrimination of complex sound signals by the auditory system in masking noise. For that, influence of masking noise on detection of shift of rippled spectrum was studied in normal listeners. The signal was a shift of ripple phase within a 0.

Spectrum pattern resolution after noise exposure in a beluga whale, Delphinapterus leucas: Evoked potential study.

Temporary threshold shift (TTS) and the discrimination of spectrum patterns after fatiguing noise exposure (170 dB re 1 μPa, 10 min duration) was investigated in a beluga whale, Delphinapterus leucas, using the evoked potential technique. Thresholds were measured using rhythmic (1000/s) pip trains of varying levels and recording the rhythmic evoked responses. Discrimination of spectrum patterns was investigated using rippled-spectrum test stimuli of various levels and ripple densities, recording the rhythmic evoked responses to ripple phase reversals.

Frequency tuning of hearing in the beluga whale: discrimination of rippled spectra.

Frequency tuning was measured in the beluga whale (Delphinapterus leucas) using rippled-noise test stimuli in conjunction with an auditory evoked potential (AEP) technique. The test stimulus was a 2-octave-wide rippled noise with frequency-proportional ripple spacing. The rippled-noise signal contained either a single reversal or rhythmic (1-kHz rate) reversals of the ripple phase.