Disparity tuning is a pervasive property of neurons in almost all visual areas in primate cortex. We will use a novel neuroimaging technique to examine the flow of disparity information from V1 to extra- striate areas in human cortex. This technique relies on source localization using high density EEG coupled to structural and functional MRI anatomical measurements. We will measure the neural response to repetitive changes in disparity in four widely separated cortical areas, V1, V3A, V4 and hMT+ - all known to be important in primate disparity processing.
Our first aim examines the sensitivity of the cortical response in these four areas to dynamic random dots, modulated by horizontal or by vertical disparity. We will also explore the response to anti-correlated random dots which are known to drive single units in many cortical areas.
Our second aim evaluates the contribution of disparity-modulation to surface segmentation. We will compare the response patterns produced by monocularly modulated changes in figure-ground segmentation to those generated by disparity modulated changes in figure-ground segmentation.
Our third aim explores how the loss of stereopsis affects the cortical responses of the strabismic observer. We will specifically look for the cortical locus of strabismic suppression, as well as for the locus of the motion asymmetry that is a defining characteristic of infantile esotropia.

Public Health Relevance

Strabismus is a developmental abnormality that affects 3 - 5% of the population, resulting in the loss of stereopsis. The proposed research will measure the cortical response associated with two anomalies of strabismus: strabismic suppression and the motion asymmetry previously observed in VEP measurements. The motion asymmetry is a useful marker for judging the efficacy of treatment, particularly surgery, so understanding its cortical origin will enhance its utility.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
3R01EY018875-01S1
Application #
7853913
Study Section
Central Visual Processing Study Section (CVP)
Program Officer
Steinmetz, Michael A
Project Start
2008-08-01
Project End
2010-05-31
Budget Start
2009-06-01
Budget End
2010-05-31
Support Year
1
Fiscal Year
2009
Total Cost
$16,656
Indirect Cost
Name
Smith-Kettlewell Eye Research Institute
Department
Type
DUNS #
073121105
City
San Francisco
State
CA
Country
United States
Zip Code
94115
Duan, Yiran; Yakovleva, Alexandra; Norcia, Anthony M (2018) Determinants of neural responses to disparity in natural scenes. J Vis 18:21
Lim, Michael; Ales, Justin M; Cottereau, Benoit R et al. (2017) Sparse EEG/MEG source estimation via a group lasso. PLoS One 12:e0176835
Norcia, Anthony M; Gerhard, Holly E; Meredith, Wesley J (2017) Development of Relative Disparity Sensitivity in Human Visual Cortex. J Neurosci 37:5608-5619
Cooper, Emily A; Norcia, Anthony M (2015) Predicting cortical dark/bright asymmetries from natural image statistics and early visual transforms. PLoS Comput Biol 11:e1004268
Cottereau, Benoit R; Ales, Justin M; Norcia, Anthony M (2015) How to use fMRI functional localizers to improve EEG/MEG source estimation. J Neurosci Methods 250:64-73
Norcia, Anthony M; Appelbaum, L Gregory; Ales, Justin M et al. (2015) The steady-state visual evoked potential in vision research: A review. J Vis 15:4
Dmochowski, Jacek P; Norcia, Anthony M (2015) Cortical Components of Reaction-Time during Perceptual Decisions in Humans. PLoS One 10:e0143339
Dmochowski, Jacek P; Greaves, Alex S; Norcia, Anthony M (2015) Maximally reliable spatial filtering of steady state visual evoked potentials. Neuroimage 109:63-72
Duan, Yiran; Norcia, Anthony M; Yeatman, Jason D et al. (2015) The Structural Properties of Major White Matter Tracts in Strabismic Amblyopia. Invest Ophthalmol Vis Sci 56:5152-60
Cottereau, Benoit R; Ales, Justin M; Norcia, Anthony M (2014) The evolution of a disparity decision in human visual cortex. Neuroimage 92:193-206

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