Literature DB >> 19757880

Cross-orientation masking is speed invariant between ocular pathways but speed dependent within them.

Tim S Meese1, Daniel H Baker.   

Abstract

In human (D. H. Baker, T. S. Meese, & R. J. Summers, 2007b) and in cat (B. Li, M. R. Peterson, J. K. Thompson, T. Duong, & R. D. Freeman, 2005; F. Sengpiel & V. Vorobyov, 2005) there are at least two routes to cross-orientation suppression (XOS): a broadband, non-adaptable, monocular (within-eye) pathway and a more narrowband, adaptable interocular (between the eyes) pathway. We further characterized these two routes psychophysically by measuring the weight of suppression across spatio-temporal frequency for cross-oriented pairs of superimposed flickering Gabor patches. Masking functions were normalized to unmasked detection thresholds and fitted by a two-stage model of contrast gain control (T. S. Meese, M. A. Georgeson, & D. H. Baker, 2006) that was developed to accommodate XOS. The weight of monocular suppression was a power function of the scalar quantity 'speed' (temporal-frequency/spatial-frequency). This weight can be expressed as the ratio of non-oriented magno- and parvo-like mechanisms, permitting a fast-acting, early locus, as benefits the urgency for action associated with high retinal speeds. In contrast, dichoptic-masking functions superimposed. Overall, this (i) provides further evidence for dissociation between the two forms of XOS in humans, and (ii) indicates that the monocular and interocular varieties of XOS are space/time scale-dependent and scale-invariant, respectively. This suggests an image-processing role for interocular XOS that is tailored to natural image statistics-very different from that of the scale-dependent (speed-dependent) monocular variety.

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Year:  2009        PMID: 19757880     DOI: 10.1167/9.5.2

Source DB:  PubMed          Journal:  J Vis        ISSN: 1534-7362            Impact factor:   2.240


  7 in total

1.  Steady-state contrast response functions provide a sensitive and objective index of amblyopic deficits.

Authors:  Daniel H Baker; Mathieu Simard; Dave Saint-Amour; Robert F Hess
Journal:  Invest Ophthalmol Vis Sci       Date:  2015-01-29       Impact factor: 4.799

2.  Psychometric functions for detection and discrimination with and without flankers.

Authors:  Miguel A García-Pérez; Rocío Alcalá-Quintana; Russell L Woods; Eli Peli
Journal:  Atten Percept Psychophys       Date:  2011-04       Impact factor: 2.199

3.  Orientation bandwidths are invariant across spatiotemporal frequency after isotropic components are removed.

Authors:  John Cass; Sjoerd Stuit; Peter Bex; David Alais
Journal:  J Vis       Date:  2009-11-23       Impact factor: 2.240

4.  Orientation-specificity of adaptation: isotropic adaptation is purely monocular.

Authors:  John Cass; Ameika Johnson; Peter J Bex; David Alais
Journal:  PLoS One       Date:  2012-11-07       Impact factor: 3.240

5.  A reevaluation of achromatic spatio-temporal vision: Nonoriented filters are monocular, they adapt, and can be used for decision making at high flicker speeds.

Authors:  Tim S Meese; Daniel H Baker
Journal:  Iperception       Date:  2011-06-21

6.  Dynamic properties of internal noise probed by modulating binocular rivalry.

Authors:  Daniel H Baker; Bruno Richard
Journal:  PLoS Comput Biol       Date:  2019-06-06       Impact factor: 4.475

7.  Contrast normalization in colour vision: the effect of luminance contrast on colour contrast detection.

Authors:  Kathy T Mullen; Yeon Jin Kim; Mina Gheiratmand
Journal:  Sci Rep       Date:  2014-12-10       Impact factor: 4.379

  7 in total

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