Hearing thresholds can be used to quantify one’s hearing ability. In various masking conditions, hearing thresholds can vary depending on the auditory cues. With comodulated masking noise and interaural phase disparity (IPD), target detection can be facilitated, lowering detection thresholds. This perceptual phenomenon is quantified as masking release: comodulation masking release (CMR) and binaural masking level difference (BMLD). As these measures only reflect the low limit of hearing, the relevance of masking release at supra-threshold levels is still unclear. Here, we used both psychoacoustic and electro-physiological measures to investigate the effect of masking release at supra-threshold levels. We investigated whether the difference in the amount of masking release will affect listening at supra-threshold levels. We used intensity just-noticeable difference (JND) to quantify n increase in the salience of the tone. As a physiological correlate of JND, we investigated late auditory evoked potentials (LAEPs) with electroencephalography (EEG). The results showed that the intensity JNDs were equal at the same intensity of the tone regardless of masking release conditions. For LAEP measures, the slope of the P2 amplitudes with a function of the level was inversely correlated with the intensity JND. In addition, the P2 amplitudes were higher in dichotic conditions compared to diotic conditions. Estimated the salience of the target tone from both experiments suggested that the salience of masked tone at supra-threshold levels may only be beneficial with BMLD.

Comodulated masking noise and binaural cues can facilitate detecting a target sound from noise. These cues can induce a decrease in detection thresholds, quantified as comodulation masking release (CMR) and binaural masking level difference (BMLD), respectively. However, their relevance to speech perception is unclear as most studies have used artificial stimuli different from speech. Here, we investigated their ecological validity using sounds with speech-like spectro-temporal dynamics. We evaluated the ecological validity of such grouping effect with stimuli reflecting formant changes in speech. We set three masker bands at formant frequencies F1, F2, and F3 based on CV combination: /gu/, /fu/, and /pu/. We found that the CMR was little (< 3 dB) while BMLD was comparable to previous findings (∼ 9 dB). In conclusion, we suggest that other features may play a role in facilitating frequency grouping by comodulation such as the spectral proximity and the number of masker bands.

When a target tone is preceded by a noise, the threshold for target detection can be increased or decreased depending on the type of a preceding masker. The effect of preceding masker to the following sound can be interpreted as either the result of adaptation at the periphery or at the system level. To disentangle these, we investigated the time constant of adaptation by varying the length of the preceding masker. For inducing various masking conditions, we designed stimuli that can induce masking release. Comodulated masking noise and binaural cues can facilitate detecting a target sound from noise. These cues induce a decrease in detection thresholds, quantified as comodulation masking release (CMR) and binaural masking level difference (BMLD), respectively. We hypothesized that if the adaptation results from the top-down processing, both CMR and BMLD will be affected with increased length of the preceding masker. We measured CMR and BMLD when the length of preceding maskers varied from 0 (no preceding masker) to 500 ms. Results showed that CMR was more affected with longer preceding masker from 100 ms to 500 ms while the preceding masker did not affect BMLD. In this study, we suggest that the adaptation to preceding masking sound may arise from low level (e.g. cochlear nucleus, CN) rather than the temporal integration by the higher-level processing.