In the sound-induced flash illusion, auditory input affects the perception of visual stimuli with a large inter- and intraindividual variability. Crossmodal influence in this illusion has been shown to be associated with activity in visual and temporal areas. In this electroencephalography study, we investigated the relationship between oscillatory brain activity prior to stimulus presentation and subsequent perception of the illusion on the level of single trials. Using logistic regression, we modeled the perceptual outcome dependent on oscillatory power. We found that 25 Hz to 41 Hz activity over occipital electrodes from 0.17 s to 0.05 s prior to stimulus onset predicted the perception of the illusion. A t-test of power values, averaged over the significant cluster, between illusion and no-illusion trials showed higher power in illusion trials, corroborating the modeling result. We conclude that the observed power modulation predisposes the integration of audiovisual signals, providing further evidence for the governing role of prestimulus brain oscillations in multisensory perception.

Interruptions in auditory input can be perceptually restored if they coincide with a masking sound, resulting in a continuity illusion. Previous studies have shown that this continuity illusion is associated with reduced low-frequency neural oscillations in the auditory cortex. However, the precise contribution of oscillatory amplitude changes and phase alignment to auditory restoration remains unclear. Using electroencephalography, we investigated induced power changes and phase locking in response to 3 Hz amplitude-modulated tones during the interval of an interrupting noise. We experimentally manipulated both the physical continuity of the tone (continuous vs. interrupted) and the masking potential of the noise (notched vs. full). We observed an attenuation of 3 Hz power during continuity illusions in comparison with both continuous tones and veridically perceived interrupted tones. This illusion-related suppression of low-frequency oscillations likely reflects a blurring of auditory object boundaries that supports continuity perception. We further observed increased 3 Hz phase locking during fully masked continuous tones compared with the other conditions. This low-frequency phase alignment may reflect the neural registration of the interrupting noise as a newly appearing object, whereas during continuity illusions, a spectral portion of this noise is delegated to filling the interruption. Taken together, our findings suggest that the suppression of slow cortical oscillations in both the power and phase domains supports perceptual restoration of interruptions in auditory input.

In the ventriloquist illusion, spatially disparate visual signals can influence the perceived location of simultaneous sounds. Previous studies have shown asymmetrical responses in auditory cortical regions following perceived peripheral sound shifts. Moreover, higher-order cortical areas perform inferences on the sources of disparate audiovisual signals. Recent studies have also highlighted top-down influence in the ventriloquist illusion and postulated a governing function of neural oscillations for crossmodal processing. In this EEG study, we analyzed source-reconstructed neural oscillations to address the question of whether perceived sound shifts affect the laterality of auditory responses. Moreover, we investigated the modulation of neural oscillations related to the occurrence of the illusion more generally. With respect to the first question, we did not find evidence for significant changes in the laterality of auditory responses due to perceived sound shifts. However, we found a sustained reduction of mediofrontal theta-band power starting prior to stimulus onset when participants perceived the illusion compared to when they did not perceive the illusion. We suggest that this effect reflects a state of diminished cognitive control, leading to reliance on more readily discriminable visual information and increased crossmodal influence. We conclude that mediofrontal theta-band oscillations serve as a neural mechanism underlying top-down modulation of crossmodal processing in the ventriloquist illusion.