Early Visual Responses Predict Conscious Face Perception within and between Subjects during Binocular Rivalry
Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170–800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivari...
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Published in | Journal of cognitive neuroscience Vol. 25; no. 6; pp. 969 - 985 |
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Main Authors | , , , , , |
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Language | English |
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01.06.2013
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Abstract | Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170–800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120–320 msec time range, peaking at the M170 around 180 msec and the P2m at around 260 msec, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. In addition, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals. |
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AbstractList | Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170–800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120–320 msec time range, peaking at the M170 around 180 msec and the P2m at around 260 msec, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. In addition, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals. Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120-320 msec time range, peaking at the M170 around 180 msec and the P2m at around 260 msec, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. In addition, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals. [PUBLICATION ABSTRACT] Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120-320 msec time range, peaking at the M170 around 180 msec and the P2m at around 260 msec, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. In addition, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals.Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800 msec after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120-320 msec time range, peaking at the M170 around 180 msec and the P2m at around 260 msec, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. In addition, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals. Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800ms after stimulus presentation, yet in the majority of these studies changes in conscious experience are confounded with changes in physical stimulation. Using multivariate classification on MEG data recorded when participants reported changes in conscious perception evoked by binocular rivalry between a face and a grating, we showed that only MEG signals in the 120-320ms time range, peaking at the M170 around 180ms and the P2m at around 260ms, reliably predicted conscious experience. Conscious perception could not only be decoded significantly better than chance from the sensors that showed the largest average difference, as previous studies suggest, but also from patterns of activity across groups of occipital sensors that individually were unable to predict perception better than chance. Additionally, source space analyses showed that sources in the early and late visual system predicted conscious perception more accurately than frontal and parietal sites, although conscious perception could also be decoded there. Finally, the patterns of neural activity associated with conscious face perception generalized from one participant to another around the times of maximum prediction accuracy. Our work thus demonstrates that the neural correlates of particular conscious contents (here, faces) are highly consistent in time and space within individuals and that these correlates are shared to some extent between individuals. |
Author | Barnes, Gareth Robert Rees, Geraint Sandberg, Kristian Overgaard, Morten Kanai, Ryota Bahrami, Bahador |
AuthorAffiliation | 3 Wellcome Trust Centre for Neuroimaging, Institute of Neurology, 12 Queen Square, WC1N 3AR London, United Kingdom 4 Interacting Minds Project, Institute of Anthropology, Archaeology, Linguistics, Aarhus University, & Centre of Functionally Integrative Neuroscience, Aarhus University Hospital, Noerrebrogade 44, Building 10 G, 8000 Aarhus C, Denmark 1 Cognitive Neuroscience Research Unit, Aarhus University Hospital, Noerrebrogade 44, Building 10G, 8000 Aarhus C, Denmark 2 UCL Institute of Cognitive Neuroscience, University College London, 17 Queen Square, WC1N 3AR London, United Kingdom |
AuthorAffiliation_xml | – name: 3 Wellcome Trust Centre for Neuroimaging, Institute of Neurology, 12 Queen Square, WC1N 3AR London, United Kingdom – name: 2 UCL Institute of Cognitive Neuroscience, University College London, 17 Queen Square, WC1N 3AR London, United Kingdom – name: 1 Cognitive Neuroscience Research Unit, Aarhus University Hospital, Noerrebrogade 44, Building 10G, 8000 Aarhus C, Denmark – name: 4 Interacting Minds Project, Institute of Anthropology, Archaeology, Linguistics, Aarhus University, & Centre of Functionally Integrative Neuroscience, Aarhus University Hospital, Noerrebrogade 44, Building 10 G, 8000 Aarhus C, Denmark |
Author_xml | – sequence: 1 givenname: Kristian surname: Sandberg fullname: Sandberg, Kristian organization: 2University College London – sequence: 2 givenname: Bahador surname: Bahrami fullname: Bahrami, Bahador organization: 3Aarhus University – sequence: 3 givenname: Ryota surname: Kanai fullname: Kanai, Ryota organization: 2University College London – sequence: 4 givenname: Gareth Robert surname: Barnes fullname: Barnes, Gareth Robert organization: 4Institute of Neurology, London, United Kingdom – sequence: 5 givenname: Morten surname: Overgaard fullname: Overgaard, Morten organization: 1Aarhus University Hospital – sequence: 6 givenname: Geraint surname: Rees fullname: Rees, Geraint organization: 4Institute of Neurology, London, United Kingdom |
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Cites_doi | 10.1523/JNEUROSCI.1575-10.2010 10.1167/8.10.4 10.1016/j.clinph.2009.08.014 10.1038/nn0602-851 10.1023/A:1017925416289 10.1016/j.cub.2005.06.026 10.1016/j.neubiorev.2009.12.002 10.1038/nature04169 10.1002/hbm.20958 10.1016/j.neuroimage.2007.09.048 10.3389/fpsyg.2011.00088 10.1167/11.10.9 10.1016/S1364-6613(00)01482-0 10.1073/pnas.2333622100 10.1126/science.146.3649.1325 10.1016/j.neuroimage.2014.06.023 10.1167/11.2.6 10.2466/pms.1963.17.2.439 10.1002/hbm.20912 10.1167/11.7.3 10.1152/jn.00557.2005 10.1162/089892904322926809 10.1167/7.8.10 10.1523/JNEUROSCI.19-13-05435.1999 10.1162/jocn_a_00189 10.1016/S0042-6989(97)00045-X 10.1073/pnas.0604673103 10.1016/j.visres.2007.07.007 10.1037/h0092990 10.1371/journal.pone.0000343 10.1046/j.1469-8986.2003.00126.x 10.1016/j.neuroimage.2004.05.008 10.1371/journal.pbio.0050260 10.1038/nn1549 10.1016/j.ijpsycho.2008.08.007 10.1126/science.280.5371.1930 10.1371/journal.pone.0001497 10.1167/8.5.4 |
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References | Babiloni (2021072913305991400_R1) 2010; 31 Liddell (2021072913305991400_R24) 2004; 16 Wilke (2021072913305991400_R36) 2006; 103 Cosmelli (2021072913305991400_R8) 2004; 23 Brascamp (2021072913305991400_R3) 2008; 3 Haynes (2021072913305991400_R18) 2005; 15 Carlson (2021072913305991400_R6) 2011; 11 Haxby (2021072913305991400_R16) 2000; 4 Carter (2021072913305991400_R7) 2007; 2 Orbach (2021072913305991400_R27) 1963; 17 Harris (2021072913305991400_R14) 2008; 8 Sandberg (2021072913305991400_R32) Wilson (2021072913305991400_R37) 2003; 100 Pegna (2021072913305991400_R29) 2008; 70 Sergent (2021072913305991400_R34) 2005; 8 Harris (2021072913305991400_R15) 2011; 11 Lansing (2021072913305991400_R22) 1964; 146 Brown (2021072913305991400_R5) 1997; 37 Wilson (2021072913305991400_R38) 2007; 47 Freeman (2021072913305991400_R12) 2005; 94 Kamphuisen (2021072913305991400_R19) 2008; 8 Sandberg (2021072913305991400_R31) 2011; 11 Srinivasan (2021072913305991400_R35) 1999; 19 Breese (2021072913305991400_R4) 1899; 3 Engell (2021072913305991400_R11) 2010; 30 Koivisto (2021072913305991400_R20) 2010; 34 Pegna (2021072913305991400_R28) 2011; 2 Lumer (2021072913305991400_R25) 1998; 280 Noest (2021072913305991400_R26) 2007; 7 Raizada (2021072913305991400_R30) 2012; 24 Friston (2021072913305991400_R13) 2008; 39 Haynes (2021072913305991400_R17) 2005; 438 Del Cul (2021072913305991400_R9) 2007; 5 Blake (2021072913305991400_R2) 2001; 2 Sarnthein (2021072913305991400_R33) 2009; 120 Leopold (2021072913305991400_R23) 2002; 5 Kornmeier (2021072913305991400_R21) 2004; 41 Duncan (2021072913305991400_R10) 2010; 31 |
References_xml | – volume: 30 start-page: 8780 year: 2010 ident: 2021072913305991400_R11 article-title: Selective attention modulates face-specific induced gamma oscillations recorded from ventral occipitotemporal cortex. publication-title: The Journal of Neuroscience: The Official Journal of the Society for Neuroscience doi: 10.1523/JNEUROSCI.1575-10.2010 – volume: 8 start-page: 4.1 year: 2008 ident: 2021072913305991400_R14 article-title: The effects of parts, wholes, and familiarity on face-selective responses in MEG. publication-title: Journal of Vision doi: 10.1167/8.10.4 – volume: 120 start-page: 1835 year: 2009 ident: 2021072913305991400_R33 article-title: High test–retest reliability of checkerboard reversal visual evoked potentials (VEP) over 8 months. publication-title: Clinical Neurophysiology doi: 10.1016/j.clinph.2009.08.014 – volume: 5 start-page: 605 year: 2002 ident: 2021072913305991400_R23 article-title: Stable perception of visually ambiguous patterns. publication-title: Nature Neuroscience doi: 10.1038/nn0602-851 – volume: 2 start-page: 5 year: 2001 ident: 2021072913305991400_R2 article-title: A primer on binocular rivalry, including current controversies. publication-title: Brain and Mind doi: 10.1023/A:1017925416289 – volume: 15 start-page: 1301 year: 2005 ident: 2021072913305991400_R18 article-title: Predicting the stream of consciousness from activity in human visual cortex. publication-title: Current Biology: CB doi: 10.1016/j.cub.2005.06.026 – volume: 34 start-page: 922 year: 2010 ident: 2021072913305991400_R20 article-title: Event-related brain potential correlates of visual awareness. publication-title: Neuroscience & Biobehavioral Reviews doi: 10.1016/j.neubiorev.2009.12.002 – volume: 438 start-page: 496 year: 2005 ident: 2021072913305991400_R17 article-title: Eye-specific effects of binocular rivalry in the human lateral geniculate nucleus. publication-title: Nature doi: 10.1038/nature04169 – volume: 31 start-page: 1556 year: 2010 ident: 2021072913305991400_R1 article-title: Cortical responses to consciousness of schematic emotional facial expressions: A high-resolution EEG study. publication-title: Human Brain Mapping doi: 10.1002/hbm.20958 – volume: 39 start-page: 1104 year: 2008 ident: 2021072913305991400_R13 article-title: Multiple sparse priors for the M/EEG inverse problem. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2007.09.048 – volume: 2 start-page: 88.1 year: 2011 ident: 2021072913305991400_R28 article-title: Early ERP modulation for task-irrelevant subliminal faces. publication-title: Frontiers in Psychology doi: 10.3389/fpsyg.2011.00088 – volume: 11 start-page: 9.1 year: 2011 ident: 2021072913305991400_R6 article-title: High temporal resolution decoding of object position and category. publication-title: Journal of Vision doi: 10.1167/11.10.9 – volume: 4 start-page: 223 year: 2000 ident: 2021072913305991400_R16 article-title: The distributed human neural system for face perception. publication-title: Trends in Cognitive Sciences doi: 10.1016/S1364-6613(00)01482-0 – volume: 100 start-page: 14499 year: 2003 ident: 2021072913305991400_R37 article-title: Computational evidence for a rivalry hierarchy in vision. publication-title: Proceedings of the National Academy of Sciences, U.S.A. doi: 10.1073/pnas.2333622100 – volume: 146 start-page: 1325 year: 1964 ident: 2021072913305991400_R22 article-title: Electroencephalographic correlates of binocular rivalry in man. publication-title: Science (New York, N.Y.) doi: 10.1126/science.146.3649.1325 – ident: 2021072913305991400_R32 article-title: Distinct MEG correlates of conscious experience, perceptual reversals, and stabilization during binocular rivalry doi: 10.1016/j.neuroimage.2014.06.023 – volume: 11 start-page: 1 year: 2011 ident: 2021072913305991400_R31 article-title: The impact of stimulus complexity and frequency swapping on stabilization of binocular rivalry. publication-title: Journal of Vision doi: 10.1167/11.2.6 – volume: 17 start-page: 439 year: 1963 ident: 2021072913305991400_R27 article-title: Reversibility of the Necker cube: I. An examination of the concept of “satiation of orientation”. publication-title: Perceptual and Motor Skills doi: 10.2466/pms.1963.17.2.439 – volume: 31 start-page: 1003 year: 2010 ident: 2021072913305991400_R10 article-title: Identifying spatially overlapping local cortical networks with MEG. publication-title: Human Brain Mapping doi: 10.1002/hbm.20912 – volume: 11 start-page: 3.1 year: 2011 ident: 2021072913305991400_R15 article-title: Sandwich masking eliminates both visual awareness of faces and face-specific brain activity through a feedforward mechanism. publication-title: Journal of Vision doi: 10.1167/11.7.3 – volume: 94 start-page: 4412 year: 2005 ident: 2021072913305991400_R12 article-title: Multistage model for binocular rivalry. publication-title: Journal of Neurophysiology doi: 10.1152/jn.00557.2005 – volume: 16 start-page: 479 year: 2004 ident: 2021072913305991400_R24 article-title: A temporal dissociation of subliminal versus supraliminal fear perception: An event-related potential study. publication-title: Journal of Cognitive Neuroscience doi: 10.1162/089892904322926809 – volume: 7 start-page: 1 year: 2007 ident: 2021072913305991400_R26 article-title: Percept-choice sequences driven by interrupted ambiguous stimuli: A low-level neural model. publication-title: Journal of Vision doi: 10.1167/7.8.10 – volume: 19 start-page: 5435 year: 1999 ident: 2021072913305991400_R35 article-title: Increased synchronization of neuromagnetic responses during conscious perception. publication-title: The Journal of Neuroscience: The Official Journal of the Society for Neuroscience doi: 10.1523/JNEUROSCI.19-13-05435.1999 – volume: 24 start-page: 868 year: 2012 ident: 2021072913305991400_R30 article-title: What makes different people's representations alike: Neural similarity space solves the problem of across-subject fMRI decoding. publication-title: Journal of Cognitive Neuroscience doi: 10.1162/jocn_a_00189 – volume: 37 start-page: 2401 year: 1997 ident: 2021072913305991400_R5 article-title: A method for investigating binocular rivalry in real-time with the steady-state VEP. publication-title: Vision Research doi: 10.1016/S0042-6989(97)00045-X – volume: 103 start-page: 17507 year: 2006 ident: 2021072913305991400_R36 article-title: Local field potential reflects perceptual suppression in monkey visual cortex. publication-title: Proceedings of the National Academy of Sciences, U.S.A. doi: 10.1073/pnas.0604673103 – volume: 47 start-page: 2741 year: 2007 ident: 2021072913305991400_R38 article-title: Minimal physiological conditions for binocular rivalry and rivalry memory. publication-title: Vision Research doi: 10.1016/j.visres.2007.07.007 – volume: 3 start-page: 1 year: 1899 ident: 2021072913305991400_R4 article-title: On inhibition. publication-title: Psychological Monographs doi: 10.1037/h0092990 – volume: 2 start-page: e343 year: 2007 ident: 2021072913305991400_R7 article-title: Onset rivalry: Brief presentation isolates an early independent phase of perceptual competition. publication-title: PloS One doi: 10.1371/journal.pone.0000343 – volume: 41 start-page: 1 year: 2004 ident: 2021072913305991400_R21 article-title: Early neural activity in Necker-cube reversal: Evidence for low-level processing of a Gestalt phenomenon. publication-title: Psychophysiology doi: 10.1046/j.1469-8986.2003.00126.x – volume: 23 start-page: 128 year: 2004 ident: 2021072913305991400_R8 article-title: Waves of consciousness: Ongoing cortical patterns during binocular rivalry. publication-title: Neuroimage doi: 10.1016/j.neuroimage.2004.05.008 – volume: 5 start-page: e260 year: 2007 ident: 2021072913305991400_R9 article-title: Brain dynamics underlying the nonlinear threshold for access to consciousness. publication-title: PLoS Biology doi: 10.1371/journal.pbio.0050260 – volume: 8 start-page: 1391 year: 2005 ident: 2021072913305991400_R34 article-title: Timing of the brain events underlying access to consciousness during the attentional blink. publication-title: Nature Neuroscience doi: 10.1038/nn1549 – volume: 70 start-page: 127 year: 2008 ident: 2021072913305991400_R29 article-title: Electrophysiological evidence for early non-conscious processing of fearful facial expressions. publication-title: International Journal of Psychophysiology doi: 10.1016/j.ijpsycho.2008.08.007 – volume: 280 start-page: 1930 year: 1998 ident: 2021072913305991400_R25 article-title: Neural correlates of perceptual rivalry in the human brain. publication-title: Science (New York, N.Y.) doi: 10.1126/science.280.5371.1930 – volume: 3 start-page: e1497 year: 2008 ident: 2021072913305991400_R3 article-title: Multi-timescale perceptual history resolves visual ambiguity. publication-title: PLoS One doi: 10.1371/journal.pone.0001497 – volume: 8 start-page: 4.1-4.8 year: 2008 ident: 2021072913305991400_R19 article-title: No evidence for widespread synchronized networks in binocular rivalry: MEG frequency tagging entrains primarily early visual cortex. publication-title: Journal of Vision doi: 10.1167/8.5.4 |
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Snippet | Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170–800 msec after stimulus... Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800 msec after stimulus... Previous studies indicate that conscious face perception may be related to neural activity in a large time window around 170-800ms after stimulus presentation,... |
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SubjectTerms | Adult Brain - physiology Classification Consciousness Consciousness - physiology Correlation analysis Eyes & eyesight Face Humans Magnetoencephalography - instrumentation Magnetoencephalography - methods Male Neurons Neuropsychological Tests Neuropsychology Pattern Recognition, Visual - physiology Sensory perception Social Perception Time Factors Vision, Binocular - physiology Young Adult |
Title | Early Visual Responses Predict Conscious Face Perception within and between Subjects during Binocular Rivalry |
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