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
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE

User menu

  • Log in
  • My Cart

Search

  • Advanced search
Journal of Neuroscience
  • 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
  • EDITORIAL BOARD
  • ABOUT
    • Overview
    • Advertise
    • For the Media
    • Rights and Permissions
    • Privacy Policy
    • Feedback
  • SUBSCRIBE
PreviousNext
Articles, Behavioral/Systems/Cognitive

The Role of Frontal and Parietal Brain Areas in Bistable Perception

Tomas Knapen, Jan Brascamp, Joel Pearson, Raymond van Ee and Randolph Blake
Journal of Neuroscience 13 July 2011, 31 (28) 10293-10301; DOI: https://doi.org/10.1523/JNEUROSCI.1727-11.2011
Tomas Knapen
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Jan Brascamp
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Joel Pearson
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Raymond van Ee
  • Find this author on Google Scholar
  • Find this author on PubMed
  • Search for this author on this site
Randolph Blake
  • 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.

    Stimuli. a, Apparent motion stimulus. A sinusoidal spiral grating was counterphased at 3–4 Hz (left), allowing for perceived motion in the clockwise and counterclockwise directions. However, in addition to these definite percepts of motion direction, participants also observed mixture percepts with no distinct motion direction during prolonged transitions, depicted here by stars (right). b, Binocular rivalry stimulus. When the two eyes are confronted with images that cannot be fused, such as red and green orthogonal gratings (left), they engage in binocular rivalry. The left and right eye image alternate in perception and prolonged transitions often take the form of a traveling wave crossing the stimulus, replacing one exclusive percept with the other.

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

    Imaging results, transition-related and transition-duration-related brain activity. a, Areas responding more strongly to transitions in bistable apparent motion than to baseline activity. b, Areas responding more strongly to bistable apparent motion transitions of longer durations than to shorter ones. These regions strongly overlap with the regions responding more to transitions than to baseline. c, Areas responding more strongly to transitions in binocular rivalry than to baseline activity. d, Areas responding more strongly to binocular rivalry transitions of longer durations than to shorter ones. These regions again show strong overlap with the regions responding more to transitions than to baseline, although this overlap does not include DLPFC or insula for this stimulus.

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

    a, Procedure. Left, Observers reported their ongoing perception of a binocular rivalry display. Right, After a short break, the reported time course was replayed on-screen to simulated perceptual transitions in one of two ways per run: as an almost instantaneous cross-fade regardless of reported duration (instantaneous replay) or as a traveling wave transition replacing one image with the other with the duration of the previously reported transition (duration-matched replay). b, Areas responding more strongly to endogenous transitions than to simulated transitions, replayed as near-instantaneous events. These regions strongly overlap with the regions responding more to transitions than to baseline (Fig. 2c) and are very similar to previous results (Lumer et al., 1998; Sterzer and Kleinschmidt, 2007). c, Areas responding more strongly to endogenous transitions than to duration-matched simulated transitions. Areas in parietal and frontal regions respond indistinguishably to endogenous and simulated transitions. d, Event-triggered averages from right frontal cortex for endogenous perceptual transitions, instantaneous replay transitions, and duration-matched replay transitions. The reason the contrast shown in c does not show frontal and parietal areas is that these event-triggered responses are almost identical.

  • Figure 4.
    • Download figure
    • Open in new tab
    • Download powerpoint
    Figure 4.

    Event-triggered results for binocular rivalry per anatomical ROI. Figure 3d gave a summary result for all relevant areas of the right frontal cortex; here we show the same result split out into more specific anatomical regions. The conclusion of Figure 3d holds for all areas within parietal and right frontal cortex. Note, however, that the event-triggered curves for areas V1–3 may seem at odds with the BOLD contrast of Figure 3c. Whereas the event-triggered curves depicted show a stronger signal for duration-matched replay than for actual binocular rivalry, the BOLD contrast between those conditions (Fig. 3c) revealed voxels in those areas for which the opposite is true. This apparent discrepancy appears to reflect different loci in these brain areas responding differently. Specifically, the activated voxels in Figure 3c correspond to a more foveal representation than the voxels that contribute importantly to the curves of V1–3 in the present plot. Like areas V1–3, extrastriate sensory areas medial temporal (MT) and lateral occipital complex (LOC) also appear to respond more strongly to our duration-matched replay condition than during rivalry. This tendency, although nonsignificant, might reflect the fact that rivalry and replay differ in the sensory stimulation provided. Error regions indicate SEM across observers.

Tables

  • Figures
  • Table 1.
    • View popup
    Table 2.

    Locations of peak Z scores in apparent motion for transition > baseline contrast

    xyzMax Z scorep value (uncorrected)
    Right DLPFC4450105.725.3 × 10−9
    Right FEF6−2565.081.9 × 10−7
    Right TPJ56−40265.267.2 × 10−8
    Right IFG5618124.973.3 × 10−7
    Right/left SPL0−70524.721.2 × 10−6
    • View popup
    Table 3.

    Locations of peak Z-scores in binocular rivalry for transition > baseline, rivalry transition > instantaneous replay transition, and rivalry transition > duration-matched replay transition contrasts

    xyzMax Z scorep value (uncorrected)
    Transition > baseline
        Right IFG5212144.807.9 × 10−7
        Right TPJ58−46464.963.5 × 10−7
        Right MT58−64−104.092.1 × 10−5
        Right FEF12−2604.681.4 × 10−6
        Right DLPFC3854224.827.2 × 10−7
        Left central sulcus−40−14464.914.6 × 10−7
    Rivalry transition > instantaneous replay transition
        Right IPS12−75523.721.0 × 10−3
        Right FEF102705.052.2 × 10−7
        Right IFG546104.151.7 × 10−5
        Right TPJ54−46344.042.7 × 10−5
        Right SPL4−62584.807.9 × 10−7
        Right DLPFC4630344.221.2 × 10−5
        Left insula−5614−24.181.5 × 10−5
        Left SPL−4−64444.721.2 × 10−6
        Left central sulcus−36−24524.904.8 × 10−7
    Rivalry transition > duration-matched replay transition
        Right occipital10−8284.221.2 × 10−5
        Left occipital−8−70−44.376.2 × 10−6
Back to top

In this issue

The Journal of Neuroscience: 31 (28)
Journal of Neuroscience
Vol. 31, Issue 28
13 Jul 2011
  • 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.
The Role of Frontal and Parietal Brain Areas in Bistable 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
The Role of Frontal and Parietal Brain Areas in Bistable Perception
Tomas Knapen, Jan Brascamp, Joel Pearson, Raymond van Ee, Randolph Blake
Journal of Neuroscience 13 July 2011, 31 (28) 10293-10301; DOI: 10.1523/JNEUROSCI.1727-11.2011

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
The Role of Frontal and Parietal Brain Areas in Bistable Perception
Tomas Knapen, Jan Brascamp, Joel Pearson, Raymond van Ee, Randolph Blake
Journal of Neuroscience 13 July 2011, 31 (28) 10293-10301; DOI: 10.1523/JNEUROSCI.1727-11.2011
del.icio.us logo Digg logo Reddit logo Twitter logo Facebook logo Google 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

  • Choice Behavior Guided by Learned, But Not Innate, Taste Aversion Recruits the Orbitofrontal Cortex
  • Maturation of Spontaneous Firing Properties after Hearing Onset in Rat Auditory Nerve Fibers: Spontaneous Rates, Refractoriness, and Interfiber Correlations
  • Insulin Treatment Prevents Neuroinflammation and Neuronal Injury with Restored Neurobehavioral Function in Models of HIV/AIDS Neurodegeneration
Show more Articles

Behavioral/Systems/Cognitive

  • The Laminar Development of Direction Selectivity in Ferret Visual Cortex
  • Individual Differences in Amygdala-Medial Prefrontal Anatomy Link Negative Affect, Impaired Social Functioning, and Polygenic Depression Risk
  • Influence of Reward on Corticospinal Excitability during Movement Preparation
Show more Behavioral/Systems/Cognitive
  • Home
  • Alerts
  • 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 Policy
  • Contact
(JNeurosci logo)
(SfN logo)

Copyright © 2023 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.