Skip to main content

Main menu

  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE

User menu

  • Log out
  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • Log out
  • Log in
  • My Cart
Journal of Neuroscience

Advanced Search

Submit a Manuscript
  • HOME
  • CONTENT
    • Early Release
    • Featured
    • Current Issue
    • Issue Archive
    • Collections
    • Podcast
  • ALERTS
  • FOR AUTHORS
    • Information for Authors
    • Fees
    • Journal Clubs
    • eLetters
    • Submit
    • Special Collections
  • EDITORIAL BOARD
    • Editorial Board
    • ECR Advisory Board
    • Journal Staff
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
    • Accessibility
  • SUBSCRIBE
PreviousNext
Articles, Behavioral/Cognitive

Binocular Rivalry: Frontal Activity Relates to Introspection and Action But Not to Perception

Stefan Frässle, Jens Sommer, Andreas Jansen, Marnix Naber and Wolfgang Einhäuser
Journal of Neuroscience 29 January 2014, 34 (5) 1738-1747; https://doi.org/10.1523/JNEUROSCI.4403-13.2014
Stefan Frässle
1Department of Neurophysics, Philipps-University, 35032 Marburg, Germany;
2Section BrainImaging, Department of Psychiatry and Psychotherapy, Philipps-University, 35037 Marburg, Germany;
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jens Sommer
2Section BrainImaging, Department of Psychiatry and Psychotherapy, Philipps-University, 35037 Marburg, Germany;
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Andreas Jansen
2Section BrainImaging, Department of Psychiatry and Psychotherapy, Philipps-University, 35037 Marburg, Germany;
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Marnix Naber
1Department of Neurophysics, Philipps-University, 35032 Marburg, Germany;
3Vision Sciences Laboratory, Harvard University, Cambridge, Massachusetts 02138;
4Cognitive Psychology Unit, Leiden University, 2333AK Leiden, The Netherlands;
5Leiden Institute for Brain and Cognition, Leiden, 2300RC Leiden, The Netherlands and
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Wolfgang Einhäuser
1Department of Neurophysics, Philipps-University, 35032 Marburg, Germany;
6Center for Interdisciplinary Research, 33615 Bielefeld, Germany
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
  • Article
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF
Loading

Article Figures & Data

Figures

  • Tables
  • Figure 1.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 1.

    Binocular rivalry and its objective measures. A, Top, Left, OKN stimulus set consisting of two distinctly colored (red/green) sinusoidal gratings that drifted in opposite lateral directions (i.e., left/right). Bottom, Left, Idealized expected OKN patterns: direction of slow phase follows the perceived direction of motion. Right, Raw horizontal gaze speed (gray), smoothed OKN slow phase speed (black), and button presses (purple vertical lines) during a typical active report rivalry OKN trial. B, Top, Left, Pupil stimulus set consisting of two stationary sinusoidal gratings that differed in orientation (i.e., ±60°), color (red/green) and luminance. Bottom, Left, Example images from eye-tracking video with pupil detection, pupil size adapts to the perceived luminance. Right, Detrended pupil size (black) and button presses (purple vertical lines) during an exemplary active report rivalry pupil trial. C, D, Average OKN speed (mean and SEM over observer median traces; C) and average pupil size (D) across observers temporally aligned to the report of a perceptual transition. The horizontal black bars indicate time periods during which traces representing a perceptual switch from percept A to percept B differed significantly from traces representing a perceptual switch from percept B to percept A. The significance criterion was adjusted to an expected false discovery rate of 0.05 (Benjamini and Hochberg, 1995) to correct for multiple comparisons. E, Median dominance durations (i.e., the time period a single percept was visible until alternated for the competing percept) for OKN and pupil trials and for the different report conditions separately. sb - w, subjective with active report; ob - w, objective with active report; ob - wo, objective with passive viewing). Dominance durations indicated by both objective indicators were shorter than those indicated by subjective report. In addition, the switch rate tended to be increased when observers had to report perceptual alternations.

  • Figure 2.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 2.

    Binocular rivalry versus replay for active report trials. A, “Discrete subjective”: activation pattern shows neural loci that were more activated time-locked to the moment of a subjective report (i.e., button press) during rivalry trials compared with replay trials. R, right hemisphere; L, left hemisphere. B, “Discrete objective”: rivalry-related activation pattern (rivalry > replay) time locked to the moment of an objective alternation (i.e., zero-crossing of OKN or pupil size traces). C, “Continuous objective”: activation pattern indicates neural loci as revealed by the complete OKN and pupil-size traces. D, Pattern indicates neural loci where statistical power was significantly increased when using the “continuous objective” analysis compared with the “discrete subjective” analysis. Results in A–D are thresholded at a conservative cluster-extent threshold of p < 0.01, FWE corrected (voxel level threshold p < 0.001, uncorrected). All active report trials are included in the analyses regardless of whether OKN or pupil stimulus set was presented. Activation patterns were rendered onto the surface of a standard anatomical template image.

  • Figure 3.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 3.

    Influence of active report on the neural network underlying binocular rivalry. A, B, Activation patterns (based on the continuous objective analysis) show neural loci that were identified to be more activated time locked to a perceptual transition during rivalry compared with replay when observers actively reported their percept (A) or just passively experienced rivalry dynamics (B). Results in A and B are thresholded at a cluster-extent threshold of p < 0.01, FWE corrected (voxel level threshold p < 0.001, uncorrected). C, Pattern indicates neural loci where rivalry-related activation (i.e., rivalry > replay) was significantly higher during active report trials compared with passive viewing trials, regardless of the objective measure OKN speed or pupil size (i.e., global null conjunction analysis). Results in C are thresholded at p < 0.001, uncorrected.

Tables

  • Figures
    • View popup
    Table 1.

    Coordinates and z-scores for transient rivalry-related activations (rivalry > replay) time locked to observers' button presses

    Cortical regionMNI coordinatesz-score
    xyz
    Rivalry > replay (button presses)
        Right superior parietal24−66466.03
        Right superior occipital26−66345.74
        Right middle occipital40−82145.72
        Right superior frontal28−2525.66
        Right inf. oper. frontal468165.27
        Right precentral38−2505.23
        Left middle occipital−38−86165.41
        Left inferior occipital−52−68−84.83
        Left cerebellum−26−70−245.05
        Right inferior frontal4042−44.47
        Right middle frontal3836324.32
    • Shown are loci where activation is greater during rivalry compared with replay. Only the most significant peaks within each area of activation are reported. All results are thresholded at a conservative cluster-extent threshold of p < 0.01, FWE corrected (voxel level threshold p < 0.001, uncorrected).

    • View popup
    Table 2.

    Coordinates and z-scores show neural loci for which the continuous objective analysis revealed higher rivalry-related activations (rivalry > replay) when observers actively reported their perception compared with when they passively experienced rivalry

    Cortical regionMNI coordinatesz-score
    xyz
    Active > passive (continuous objective analysis)
        Left superior frontal−204604.31
        Left suppl. motor area−612503.74
        Left middle occipital−20−60364.24
        Left superior parietal−16−58483.98
        Left middle frontal−3632244.24
        Right insula3024104.09
        Left insula−2822124.06
        Left middle temporal−44−6083.99
        Right middle frontal4040343.98
        Right inferior frontal (tris.)4036263.71
        Right superior frontal3044323.41
        Left inferior parietal−52−42383.93
        Right sup. medial frontal824483.91
        Right middle occipital32−74123.74
        Right suppl. motor area1010563.71
        Right precuneus8−54663.68
        Left calcarine−26−60163.30
    • Loci were identified in terms of a global null conjunction analysis to control for any indicator-related artifacts. Therefore, the linear contrast “rivalry > replay” was calculated for each report and indicator condition in every observer separately. Those contrast images entered a random-effects group analysis in which the neural loci were assessed that had higher rivalry-related activation during active report compared with passive viewing trials regardless of rivalry type. Only the most significant peaks within each area of activation are reported and only clusters exceeding 20 voxels in size are reported. All results are thresholded at p < 0.001, uncorrected.

Back to top

In this issue

The Journal of Neuroscience: 34 (5)
Journal of Neuroscience
Vol. 34, Issue 5
29 Jan 2014
  • Table of Contents
  • Table of Contents (PDF)
  • About the Cover
  • Index by author
  • Advertising (PDF)
  • Ed Board (PDF)
Email

Thank you for sharing this Journal of Neuroscience article.

NOTE: We request your email address only to inform the recipient that it was you who recommended this article, and that it is not junk mail. We do not retain these email addresses.

Enter multiple addresses on separate lines or separate them with commas.
Binocular Rivalry: Frontal Activity Relates to Introspection and Action But Not to Perception
(Your Name) has forwarded a page to you from Journal of Neuroscience
(Your Name) thought you would be interested in this article in Journal of Neuroscience.
CAPTCHA
This question is for testing whether or not you are a human visitor and to prevent automated spam submissions.
Print
View Full Page PDF
Citation Tools
Binocular Rivalry: Frontal Activity Relates to Introspection and Action But Not to Perception
Stefan Frässle, Jens Sommer, Andreas Jansen, Marnix Naber, Wolfgang Einhäuser
Journal of Neuroscience 29 January 2014, 34 (5) 1738-1747; DOI: 10.1523/JNEUROSCI.4403-13.2014

Citation Manager Formats

  • BibTeX
  • Bookends
  • EasyBib
  • EndNote (tagged)
  • EndNote 8 (xml)
  • Medlars
  • Mendeley
  • Papers
  • RefWorks Tagged
  • Ref Manager
  • RIS
  • Zotero
Respond to this article
Request Permissions
Share
Binocular Rivalry: Frontal Activity Relates to Introspection and Action But Not to Perception
Stefan Frässle, Jens Sommer, Andreas Jansen, Marnix Naber, Wolfgang Einhäuser
Journal of Neuroscience 29 January 2014, 34 (5) 1738-1747; DOI: 10.1523/JNEUROSCI.4403-13.2014
Twitter logo Facebook logo Mendeley logo
  • Tweet Widget
  • Facebook Like
  • Google Plus One

Jump to section

  • Article
    • Abstract
    • Introduction
    • Materials and Methods
    • Results
    • Discussion
    • Footnotes
    • References
  • Figures & Data
  • Info & Metrics
  • eLetters
  • PDF

Responses to this article

Respond to this article

Jump to comment:

No eLetters have been published for this article.

Related Articles

Cited By...

More in this TOC Section

Articles

  • Memory Retrieval Has a Dynamic Influence on the Maintenance Mechanisms That Are Sensitive to ζ-Inhibitory Peptide (ZIP)
  • Neurophysiological Evidence for a Cortical Contribution to the Wakefulness-Related Drive to Breathe Explaining Hypocapnia-Resistant Ventilation in Humans
  • Monomeric Alpha-Synuclein Exerts a Physiological Role on Brain ATP Synthase
Show more Articles

Behavioral/Cognitive

  • Behavior-Relevant Periodized Neural Representation of Acoustic But Not Tactile Rhythm in Humans
  • Neural Sensitivity to the Heartbeat Is Modulated by Fluctuations in Affective Arousal during Spontaneous Thought
  • Medial Frontal Theta Reduction Impairs Rule Switching via Prediction Error
Show more Behavioral/Cognitive
  • Home
  • Alerts
  • Follow SFN on BlueSky
  • Visit Society for Neuroscience on Facebook
  • Follow Society for Neuroscience on Twitter
  • Follow Society for Neuroscience on LinkedIn
  • Visit Society for Neuroscience on Youtube
  • Follow our RSS feeds

Content

  • Early Release
  • Current Issue
  • Issue Archive
  • Collections

Information

  • For Authors
  • For Advertisers
  • For the Media
  • For Subscribers

About

  • About the Journal
  • Editorial Board
  • Privacy Notice
  • Contact
  • Accessibility
(JNeurosci logo)
(SfN logo)

Copyright © 2025 by the Society for Neuroscience.
JNeurosci Online ISSN: 1529-2401

The ideas and opinions expressed in JNeurosci do not necessarily reflect those of SfN or the JNeurosci Editorial Board. Publication of an advertisement or other product mention in JNeurosci should not be construed as an endorsement of the manufacturer’s claims. SfN does not assume any responsibility for any injury and/or damage to persons or property arising from or related to any use of any material contained in JNeurosci.