The actionable space surrounding the body, referred to as peripersonal space (PPS), has been the subject of significant interest of late within the broader framework of embodied cognition. Neurophysiological and neuroimaging studies have shown the representation of PPS to be built from visuotactile and audiotactile neurons within a frontoparietal network and whose activity is modulated by the presence of stimuli in proximity to the body. In contrast to single-unit and fMRI studies, an area of inquiry that has received little attention is the EEG characterization associated with PPS processing. Furthermore, although PPS is encoded by multisensory neurons, to date there has been no EEG study systematically examining neural responses to unisensory and multisensory stimuli, as these are presented outside, near, and within the boundary of PPS. Similarly, it remains poorly understood whether multisensory integration is generally more likely at certain spatial locations (e.g., near the body) or whether the cross-modal tactile facilitation that occurs within PPS is simply due to a reduction in the distance between sensory stimuli when close to the body and in line with the spatial principle of multisensory integration. In the current study, to examine the neural dynamics of multisensory processing within and beyond the PPS boundary, we present auditory, visual, and audiovisual stimuli at various distances relative to participants' reaching limit—an approximation of PPS—while recording continuous high-density EEG. We question whether multisensory (vs. unisensory) processing varies as a function of stimulus–observer distance. Results demonstrate a significant increase of global field power (i.e., overall strength of response across the entire electrode montage) for stimuli presented at the PPS boundary—an increase that is largest under multisensory (i.e., audiovisual) conditions. Source localization of the major contributors to this global field power difference suggests neural generators in the intraparietal sulcus and insular cortex, hubs for visuotactile and audiotactile PPS processing. Furthermore, when neural dynamics are examined in more detail, changes in the reliability of evoked potentials in centroparietal electrodes are predictive on a subject-by-subject basis of the later changes in estimated current strength at the intraparietal sulcus linked to stimulus proximity to the PPS boundary. Together, these results provide a previously unrealized view into the neural dynamics and temporal code associated with the encoding of nontactile multisensory around the PPS boundary.

Most evidence on the neural and perceptual correlates of sensory processing derives from studies that have focused on only a single sensory modality and averaged the data from groups of participants. Although valuable, such studies ignore the substantial interindividual and intraindividual differences that are undoubtedly at play. Such variability plays an integral role in both the behavioral/perceptual realms and in the neural correlates of these processes, but substantially less is known when compared with group-averaged data. Recently, it has been shown that the presentation of stimuli from two or more sensory modalities (i.e., multisensory stimulation) not only results in the well-established performance gains but also gives rise to reductions in behavioral and neural response variability. To better understand the relationship between neural and behavioral response variability under multisensory conditions, this study investigated both behavior and brain activity in a task requiring participants to discriminate moving versus static stimuli presented in either a unisensory or multisensory context. EEG data were analyzed with respect to intraindividual and interindividual differences in RTs. The results showed that trial-by-trial variability of RTs was significantly reduced under audiovisual presentation conditions as compared with visual-only presentations across all participants. Intraindividual variability of RTs was linked to changes in correlated activity between clusters within an occipital to frontal network. In addition, interindividual variability of RTs was linked to differential recruitment of medial frontal cortices. The present findings highlight differences in the brain networks that support behavioral benefits during unisensory versus multisensory motion detection and provide an important view into the functional dynamics within neuronal networks underpinning intraindividual performance differences.

The neural underpinnings of perceptual awareness have been extensively studied using unisensory (e.g., visual alone) stimuli. However, perception is generally multisensory, and it is unclear whether the neural architecture uncovered in these studies directly translates to the multisensory domain. Here, we use EEG to examine brain responses associated with the processing of visual, auditory, and audiovisual stimuli presented near threshold levels of detectability, with the aim of deciphering similarities and differences in the neural signals indexing the transition into perceptual awareness across vision, audition, and combined visual–auditory (multisensory) processing. More specifically, we examine (1) the presence of late evoked potentials (∼>300 msec), (2) the across-trial reproducibility, and (3) the evoked complexity associated with perceived versus nonperceived stimuli. Results reveal that, although perceived stimuli are associated with the presence of late evoked potentials across each of the examined sensory modalities, between-trial variability and EEG complexity differed for unisensory versus multisensory conditions. Whereas across-trial variability and complexity differed for perceived versus nonperceived stimuli in the visual and auditory conditions, this was not the case for the multisensory condition. Taken together, these results suggest that there are fundamental differences in the neural correlates of perceptual awareness for unisensory versus multisensory stimuli. Specifically, the work argues that the presence of late evoked potentials, as opposed to neural reproducibility or complexity, most closely tracks perceptual awareness regardless of the nature of the sensory stimulus. In addition, the current findings suggest a greater similarity between the neural correlates of perceptual awareness of unisensory (visual and auditory) stimuli when compared with multisensory stimuli.

Multisensory integration of visual mouth movements with auditory speech is known to offer substantial perceptual benefits, particularly under challenging (i.e., noisy) acoustic conditions. Previous work characterizing this process has found that ERPs to auditory speech are of shorter latency and smaller magnitude in the presence of visual speech. We sought to determine the dependency of these effects on the temporal relationship between the auditory and visual speech streams using EEG. We found that reductions in ERP latency and suppression of ERP amplitude are maximal when the visual signal precedes the auditory signal by a small interval and that increasing amounts of asynchrony reduce these effects in a continuous manner. Time–frequency analysis revealed that these effects are found primarily in the theta (4–8 Hz) and alpha (8–12 Hz) bands, with a central topography consistent with auditory generators. Theta effects also persisted in the lower portion of the band (3.5–5 Hz), and this late activity was more frontally distributed. Importantly, the magnitude of these late theta oscillations not only differed with the temporal characteristics of the stimuli but also served to predict participants' task performance. Our analysis thus reveals that suppression of single-trial brain responses by visual speech depends strongly on the temporal concordance of the auditory and visual inputs. It further illustrates that processes in the lower theta band, which we suggest as an index of incongruity processing, might serve to reflect the neural correlates of individual differences in multisensory temporal perception.

Visual and auditory cortices traditionally have been considered to be “modality-specific.” Thus, their activity has been thought to be unchanged by information in other sensory modalities. However, using functional magnetic resonance imaging (fMRI), the present experiments revealed that ongoing activity in the visual cortex could be modulated by auditory information and ongoing activity in the auditory cortex could be modulated by visual information. In both cases, this cross-modal modulation of activity took the form of deactivation. Yet, the deactivation response was not evident in either cortical area during the paired presentation of visual and auditory stimuli. These data suggest that cross-modal inhibitory processes operate within traditional modality-specific cortices and that these processes can be switched on or off in different circumstances.