Literature DB >> 28434862

Consequences of the Oculomotor Cycle for the Dynamics of Perception.

Marco Boi1, Martina Poletti1, Jonathan D Victor2, Michele Rucci3.   

Abstract

Much evidence indicates that humans and other species process large-scale visual information before fine spatial detail. Neurophysiological data obtained with paralyzed eyes suggest that this coarse-to-fine sequence results from spatiotemporal filtering by neurons in the early visual pathway. However, the eyes are normally never stationary: rapid gaze shifts (saccades) incessantly alternate with slow fixational movements. To investigate the consequences of this oculomotor cycle on the dynamics of perception, we combined spectral analysis of visual input signals, neural modeling, and gaze-contingent control of retinal stimulation in humans. We show that the saccade/fixation cycle reformats the flow impinging on the retina in a way that initiates coarse-to-fine processing at each fixation. This finding reveals that the visual system uses oculomotor-induced temporal modulations to sequentially encode different spatial components and suggests that, rather than initiating coarse-to-fine processing, spatiotemporal coupling in the early visual pathway builds on the information dynamics of the oculomotor cycle.
Copyright © 2017 Elsevier Ltd. All rights reserved.

Entities:  

Keywords:  coarse-to-fine; contrast sensitivity; fixational eye movements; magnocellular; microsaccade; ocular drift; parvocellular; retina; saccade; spatial vision

Mesh:

Year:  2017        PMID: 28434862      PMCID: PMC5975250          DOI: 10.1016/j.cub.2017.03.034

Source DB:  PubMed          Journal:  Curr Biol        ISSN: 0960-9822            Impact factor:   10.834


  41 in total

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  19 in total

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Review 8.  Stimulus- and goal-oriented frameworks for understanding natural vision.

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9.  Transient perceptual enhancements resulting from selective shifts of exogenous attention in the central fovea.

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10.  Microsaccade-rhythmic modulation of neural synchronization and coding within and across cortical areas V1 and V2.

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