ArticleJournal of cognitive neuroscience2018
Probing Electrophysiological Indices of Perceptual Awareness across Unisensory and Multisensory Modalities.
Article in Journal of cognitive neuroscience, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.
What it found
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Who cites it
8 citing papers in PubMed.
- Stimulus-driven and behavior-driving activity along the cortical auditory hierarchy.NeuroImage · 2026Article
- Article
- Consciousness and Energy Processing in Neural Systems.Brain sciences · 2024Article
- Bifurcation in brain dynamics reveals a signature of conscious processing independent of report.Nature communications · 2021Article
- Rapid Recalibration of Peri-Personal Space: Psychophysical, Electrophysiological, and Neural Network Modeling Evidence.Cerebral cortex (New York, N.Y. : 1991) · 2020Article
- Review
- Leveraging Nonhuman Primate Multisensory Neurons and Circuits in Assessing Consciousness Theory.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2019Article
- Peri-personal space encoding in patients with disorders of consciousness and cognitive-motor dissociation.NeuroImage. Clinical · 2019Article
Corrections and comments
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Authors and funding
6 authors.
Funding
Abstract
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.
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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.