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Neuronal mechanisms underlying differences in spatial resolution between darks and lights in human vision
Author(s) -
Carmen Pons,
Reece Mazade,
Jianzhong Jin,
Mitchell W. Dul,
Qasim Zaidi,
JoséManuel Alonso
Publication year - 2017
Publication title -
journal of vision
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.126
H-Index - 113
ISSN - 1534-7362
DOI - 10.1167/17.14.5
Subject(s) - luminance , mesopic vision , salience (neuroscience) , optics , stimulus (psychology) , physics , visual cortex , perception , artificial intelligence , photic stimulation , computer vision , neuroscience , visual perception , psychology , computer science , retina , cognitive psychology , photopic vision
Artists and astronomers noticed centuries ago that humans perceive dark features in an image differently from light ones; however, the neuronal mechanisms underlying these dark/light asymmetries remained unknown. Based on computational modeling of neuronal responses, we have previously proposed that such perceptual dark/light asymmetries originate from a luminance/response saturation within the ON retinal pathway. Consistent with this prediction, here we show that stimulus conditions that increase ON luminance/response saturation (e.g., dark backgrounds) or its effect on light stimuli (e.g., optical blur) impair the perceptual discrimination and salience of light targets more than dark targets in human vision. We also show that, in cat visual cortex, the magnitude of the ON luminance/response saturation remains relatively constant under a wide range of luminance conditions that are common indoors, and only shifts away from the lowest luminance contrasts under low mesopic light. Finally, we show that the ON luminance/response saturation affects visual salience mostly when the high spatial frequencies of the image are reduced by poor illumination or optical blur. Because both low luminance and optical blur are risk factors in myopia, our results suggest a possible neuronal mechanism linking myopia progression with the function of the ON visual pathway.

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