Literature DB >> 9643554

Neural mechanisms underlying stereoscopic vision.

F Gonzalez1, R Perez.   

Abstract

The progressive frontalization of both eyes in mammals causes overlap of the left and right visual fields, having as a consequence a region of binocular field with single vision and stereopsis. The horizontal separation of the eyes makes the retinal images of the objects lying in this binocular field have slight horizontal and vertical differences, termed disparities. Horizontal disparities are the main cue for stereopsis. In the past decades numerous physiological studies made on monkeys, which have in many aspects a similar visual system to humans, showed that a population of visual cells are capable of encoding the amplitude and sign of horizontal disparity. Such disparity detectors were found in cortical visual areas V1, V2, V3, V3A, VP, MT (V5) and MST of monkeys and in the superior colliculus of the cat and opossum. According to their disparity tuning function, these cells were first grouped into tuned excitatory, tuned inhibitory, near and far sub-groups. Subsequent studies added two more categories, tuned near and tuned far cells. Asymmetries between left and right receptive field position, on and off regions, and intra-receptive field wiring are believed to be the neural mechanisms of disparity detection. Because horizontal disparity alone is insufficient to compute reliable stereopsis, additional information about fixation distance and angle of gaze is required. Thus, while there is unequivocal evidence of cells capable of detecting horizontal disparities, it is not known how horizontal disparity is calibrated. Sensitivity to vertical disparity and information about the vergence angle or eye position may be the source of this additional information.

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Mesh:

Year:  1998        PMID: 9643554     DOI: 10.1016/s0301-0082(98)00012-4

Source DB:  PubMed          Journal:  Prog Neurobiol        ISSN: 0301-0082            Impact factor:   11.685


  30 in total

Review 1.  Early computational processing in binocular vision and depth perception.

Authors:  Jenny Read
Journal:  Prog Biophys Mol Biol       Date:  2005-01       Impact factor: 3.667

2.  Pupillary response induced by stereoscopic stimuli.

Authors:  Zhi Li; Fuchuan Sun
Journal:  Exp Brain Res       Date:  2004-12-03       Impact factor: 1.972

3.  Visual and vergence eye movement-related responses of pursuit neurons in the caudal frontal eye fields to motion-in-depth stimuli.

Authors:  Teppei Akao; Sergei A Kurkin; Junko Fukushima; Kikuro Fukushima
Journal:  Exp Brain Res       Date:  2005-05-28       Impact factor: 1.972

4.  Properties of pupillary responses to dynamic random-dot stereograms.

Authors:  Zhi Li; Peiji Liang; Fuchuan Sun
Journal:  Exp Brain Res       Date:  2005-12-02       Impact factor: 1.972

5.  Coding of stereoscopic depth information in visual areas V3 and V3A.

Authors:  Akiyuki Anzai; Syed A Chowdhury; Gregory C DeAngelis
Journal:  J Neurosci       Date:  2011-07-13       Impact factor: 6.167

6.  Binocular summation for reflexive eye movements.

Authors:  Christian Quaia; Lance M Optican; Bruce G Cumming
Journal:  J Vis       Date:  2018-04-01       Impact factor: 2.240

7.  Effects of diazepam on the latency of saccades for luminance and binocular disparity defined stimuli.

Authors:  Cunguo Wang; Jianliang Tong; Fuchuan Sun
Journal:  Exp Brain Res       Date:  2005-04-08       Impact factor: 1.972

8.  A map for horizontal disparity in monkey V2.

Authors:  Gang Chen; Haidong D Lu; Anna W Roe
Journal:  Neuron       Date:  2008-05-08       Impact factor: 17.173

9.  Understanding the cortical specialization for horizontal disparity.

Authors:  Jenny C A Read; Bruce G Cumming
Journal:  Neural Comput       Date:  2004-10       Impact factor: 2.026

10.  Latency of adaptive vergence eye movements induced by vergence-vestibular interaction training in monkeys.

Authors:  Teppei Akao; Sergei Kurkin; Kikuro Fukushima
Journal:  Exp Brain Res       Date:  2004-07-14       Impact factor: 1.972

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