Activity in the Visual Cortex is Modulated by Top-Down Attention Locked to Reaction Time

We studied the correlation between perception and hemodynamic activity in the visual cortex in a change detection task. Whenever the observer perceived the location of a change, rightly or wrongly, the blood oxygenation level-dependent signal increased in the primary visual cortex and the nearby extrastriate areas above the baseline activity caused by the visual stimulation. This non-sensory-evoked activity was localized and corresponded to the perceived location of the change. When a change was missed, or when observers attended to a different task, the change failed to evoke such a response. The latency of the nonsensory component increased linearly with subjects' reaction time, with a slope of one, and its amplitude was independent of contrast. Control experiments are compatible with the hypothesis that the nonsensory hemodynamic signal is mediated by top-down spatial attention, linked to (but separate from) awareness of the change.

[1]  Lamme Vaf,et al.  Why visual attention and awareness are different , 2003 .

[2]  D. Heeger,et al.  Neuronal activity in human primary visual cortex correlates with perception during binocular rivalry , 2000, Nature Neuroscience.

[3]  K Ugurbil,et al.  Human primary visual cortex and lateral geniculate nucleus activation during visual imagery , 1998, Neuroreport.

[4]  S. Engel,et al.  Interocular rivalry revealed in the human cortical blind-spot representation , 2001, Nature.

[5]  S Thesen,et al.  Prospective acquisition correction for head motion with image‐based tracking for real‐time fMRI , 2000, Magnetic resonance in medicine.

[6]  R. Blake,et al.  V1 activity is reduced during binocular rivalry. , 2002, Journal of vision.

[7]  C. Koch,et al.  Attention and consciousness: two distinct brain processes , 2007, Trends in Cognitive Sciences.

[8]  C. Koch,et al.  Are we aware of neural activity in primary visual cortex? , 1995, Nature.

[9]  C. Frith,et al.  Neural correlates of change detection and change blindness , 2001, Nature Neuroscience.

[10]  C. Koch The quest for consciousness : a neurobiological approach , 2004 .

[11]  David J. Heeger,et al.  Neuronal correlates of perception in early visual cortex , 2003, Nature Neuroscience.

[12]  J. Changeux,et al.  Ongoing Spontaneous Activity Controls Access to Consciousness: A Neuronal Model for Inattentional Blindness , 2005, PLoS biology.

[13]  S. Kastner,et al.  Stimulus context modulates competition in human extrastriate cortex , 2005, Nature Neuroscience.

[14]  D H Brainard,et al.  The Psychophysics Toolbox. , 1997, Spatial vision.

[15]  Ronald A. Rensink Change detection. , 2002, Annual review of psychology.

[16]  Ravi S. Menon,et al.  Mental chronometry using latency-resolved functional MRI. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[17]  Ronald A. Rensink,et al.  TO SEE OR NOT TO SEE: The Need for Attention to Perceive Changes in Scenes , 1997 .

[18]  Lars Muckli,et al.  Primary Visual Cortex Activity along the Apparent-Motion Trace Reflects Illusory Perception , 2005, PLoS biology.

[19]  Thomas Dierks,et al.  Tracking the Mind's Image in the Brain II Transcranial Magnetic Stimulation Reveals Parietal Asymmetry in Visuospatial Imagery , 2002, Neuron.

[20]  F. Tong,et al.  Decoding the visual and subjective contents of the human brain , 2005, Nature Neuroscience.

[21]  Scott A. Huettel,et al.  Dissociating the Neural Mechanisms of Visual Attention in Change Detection Using Functional MRI , 2001, Journal of Cognitive Neuroscience.

[22]  Leslie G. Ungerleider,et al.  Increased Activity in Human Visual Cortex during Directed Attention in the Absence of Visual Stimulation , 1999, Neuron.

[23]  A. Dale,et al.  The Retinotopy of Visual Spatial Attention , 1998, Neuron.

[24]  E. DeYoe,et al.  A physiological correlate of the 'spotlight' of visual attention , 1999, Nature Neuroscience.

[25]  D. Heeger,et al.  Activity in primary visual cortex predicts performance in a visual detection task , 2000, Nature Neuroscience.

[26]  G. Glover,et al.  Retinotopic organization in human visual cortex and the spatial precision of functional MRI. , 1997, Cerebral cortex.

[27]  Leslie G. Ungerleider,et al.  Neural correlates of change detection and change blindness in a working memory task. , 2004, Cerebral cortex.

[28]  Byoung-Kyong Min,et al.  Prestimulus EEG alpha activity reflects temporal expectancy , 2008, Neuroscience Letters.

[29]  M. Carrasco,et al.  Transient Attention Enhances Perceptual Performance and fMRI Response in Human Visual Cortex , 2005, Neuron.

[30]  A. Grinvald,et al.  Spontaneously emerging cortical representations of visual attributes , 2003, Nature.

[31]  R. Goebel,et al.  Tracking the Mind's Image in the Brain I Time-Resolved fMRI during Visuospatial Mental Imagery , 2002, Neuron.

[32]  J W Belliveau,et al.  Borders of multiple visual areas in humans revealed by functional magnetic resonance imaging. , 1995, Science.

[33]  V. Lamme,et al.  The distinct modes of vision offered by feedforward and recurrent processing , 2000, Trends in Neurosciences.

[34]  Vincent Walsh,et al.  Right parietal cortex plays a critical role in change blindness. , 2006, Cerebral cortex.

[35]  Michael Brady,et al.  Improved Optimization for the Robust and Accurate Linear Registration and Motion Correction of Brain Images , 2002, NeuroImage.