Using intrinsic signal optical imaging, Chen et al. (1) show that disparity information in visual area V2 is decodable from correlated random dot stereograms (cRDSs), but not from anticorrelated RDSs (aRDSs). The authors conclude that "V2 is the initial locus of false matching elimination," indicating that the correspondence problem is solved within or immediately after V2. We disagree with this conclusion based on previous single-unit studies. Two immediate downstream areas of V2, middle temporal area (MT) and V4, still encode disparities of aRDSs. Anticorrelation reduces the disparity selectivity by only ∼50% in MT (2, 3) and ∼60% in V4 (3, 4) (as evaluated by the mean amplitude ratio between the tuning curves for aRDSs and cRDSs). These findings suggest that the stereo correspondence problem is not yet fully solved within or immediately after V2. Although direct projections from V1 to MT might explain retained selectivity in MT (1), this same explanation is less plausible in V4. Relative disparity selectivity progressively develops from V1 through V2 to V4 (5-7), suggesting that V2 is an important area bridging V1 and V4 in disparity processing. Therefore, we suspect that artificial pooling inherent to intrinsic signal optical imaging may have attenuated false-match responses to a greater degree than biological pooling between V2 and V4. Chen et al. list several parameters over which pooling may reduce the responses to false matches. These parameters include preferred orientations, spatial scales, and receptive-field locations. We propose to add another important parameter to this list: the difference in tuning shape (phase) for cRDSs and aRDSs. Fig. 1 depicts a scenario that can explain