Literature DB >> 12742108

Short-latency ocular following in humans is dependent on absolute (rather than relative) binocular disparity.

D-S Yang1, F A Miles.   

Abstract

A previous study showed that the initial ocular following responses elicited by sudden motion of a large random-dot pattern were only modestly attenuated when that whole pattern was shifted out of the plane of fixation by altering its horizontal binocular disparity, but the same disparity applied to a restricted region of the dots had a much more powerful effect [Vision Research 41 (2001) 3371]. Thus, if the dots were partitioned into horizontal bands, for example, and alternate bands were moved in opposite directions to the left or right then ocular following was very weak, but if the (conditioning) dots moving in one direction were all shifted out of the plane of fixation (by applying horizontal disparity to them) then strong ocular following was now seen in the direction of motion of the (test) dots in the plane of fixation, i.e., moving images became much less effective when they were given binocular disparity. We sought to determine if the greater impact of disparity with the partitioned images was because there were additional relative disparity cues. We used a similar partitioned display and found that the dependence of ocular following on the absolute disparity of the conditioning stimulus had a Gaussian form with an x-offset that was close to zero disparity and, importantly, this offset was almost unaffected by changing the absolute disparity of the test stimulus. We conclude from this that it is the absolute--rather than the relative--disparity that is important, and that ocular following has a strong preference for moving images whose absolute disparities are close to zero. This is consistent with the idea that ocular following selectively stabilizes the retinal images of objects in and around the plane of fixation and works in harmony with disparity vergence, which uses absolute disparity to bring objects of interest into the plane of fixation [Archives of Ophthalmology 55 (1956) 848].

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Year:  2003        PMID: 12742108      PMCID: PMC2426753          DOI: 10.1016/s0042-6989(03)00146-9

Source DB:  PubMed          Journal:  Vision Res        ISSN: 0042-6989            Impact factor:   1.886


  44 in total

1.  A specialization for relative disparity in V2.

Authors:  O M Thomas; B G Cumming; A J Parker
Journal:  Nat Neurosci       Date:  2002-05       Impact factor: 24.884

2.  Short-latency disparity-vergence eye movements in humans: sensitivity to simulated orthogonal tropias.

Authors:  D-S Yang; E J FitzGibbon; F A Miles
Journal:  Vision Res       Date:  2003-02       Impact factor: 1.886

3.  Disparity sensitivity of neurons in monkey extrastriate area MST.

Authors:  J P Roy; H Komatsu; R H Wurtz
Journal:  J Neurosci       Date:  1992-07       Impact factor: 6.167

4.  Organization of disparity-selective neurons in macaque area MT.

Authors:  G C DeAngelis; W T Newsome
Journal:  J Neurosci       Date:  1999-02-15       Impact factor: 6.167

5.  Short-latency ocular following responses of monkey. I. Dependence on temporospatial properties of visual input.

Authors:  F A Miles; K Kawano; L M Optican
Journal:  J Neurophysiol       Date:  1986-11       Impact factor: 2.714

6.  Neural activity in cortical area MST of alert monkey during ocular following responses.

Authors:  K Kawano; M Shidara; Y Watanabe; S Yamane
Journal:  J Neurophysiol       Date:  1994-06       Impact factor: 2.714

7.  Eye movements and stereopsis during dichoptic viewing of moving random-dot stereograms.

Authors:  C J Erkelens; H Collewijn
Journal:  Vision Res       Date:  1985       Impact factor: 1.886

8.  Direction- and velocity-specific responses from beyond the classical receptive field in the middle temporal visual area (MT).

Authors:  J Allman; F Miezin; E McGuinness
Journal:  Perception       Date:  1985       Impact factor: 1.490

9.  The middle temporal visual area in the macaque: myeloarchitecture, connections, functional properties and topographic organization.

Authors:  D C Van Essen; J H Maunsell; J L Bixby
Journal:  J Comp Neurol       Date:  1981-07-01       Impact factor: 3.215

Review 10.  The neural processing of 3-D visual information: evidence from eye movements.

Authors:  F A Miles
Journal:  Eur J Neurosci       Date:  1998-03       Impact factor: 3.386

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  14 in total

1.  The initial ocular following responses elicited by apparent-motion stimuli: reversal by inter-stimulus intervals.

Authors:  B M Sheliga; K J Chen; E J FitzGibbon; F A Miles
Journal:  Vision Res       Date:  2005-10-18       Impact factor: 1.886

Review 2.  Initial ocular following in humans depends critically on the fourier components of the motion stimulus.

Authors:  K J Chen; B M Sheliga; E J Fitzgibbon; F A Miles
Journal:  Ann N Y Acad Sci       Date:  2005-04       Impact factor: 5.691

3.  Initial ocular following in humans: a response to first-order motion energy.

Authors:  B M Sheliga; K J Chen; E J Fitzgibbon; F A Miles
Journal:  Vision Res       Date:  2005-11       Impact factor: 1.886

4.  Deficits in short-latency tracking eye movements after chemical lesions in monkey cortical areas MT and MST.

Authors:  Aya Takemura; Yumi Murata; Kenji Kawano; F A Miles
Journal:  J Neurosci       Date:  2007-01-17       Impact factor: 6.167

5.  Rotational and translational optokinetic nystagmus have different kinematics.

Authors:  Jing Tian; David S Zee; Mark F Walker
Journal:  Vision Res       Date:  2007-02-22       Impact factor: 1.886

6.  The vergence eye movements induced by radial optic flow: some fundamental properties of the underlying local-motion detectors.

Authors:  Y Kodaka; B M Sheliga; E J FitzGibbon; F A Miles
Journal:  Vision Res       Date:  2007-08-15       Impact factor: 1.886

7.  Spatial summation properties of the human ocular following response (OFR): evidence for nonlinearities due to local and global inhibitory interactions.

Authors:  B M Sheliga; E J Fitzgibbon; F A Miles
Journal:  Vision Res       Date:  2008-07-07       Impact factor: 1.886

8.  Effect of binocular rivalry suppression on initial ocular following responses.

Authors:  Mingxia Zhu; Richard W Hertle; Chang H Kim; Xuefeng Shi; Dongsheng Yang
Journal:  J Vis       Date:  2008-04-23       Impact factor: 2.240

9.  Contrast sensitivity, first-order motion and Initial ocular following in demyelinating optic neuropathy.

Authors:  Janet C Rucker; Boris M Sheliga; Edmond J Fitzgibbon; Frederick A Miles; R John Leigh
Journal:  J Neurol       Date:  2006-04-28       Impact factor: 4.849

10.  Human ocular following initiated by competing image motions: evidence for a winner-take-all mechanism.

Authors:  B M Sheliga; Y Kodaka; E J FitzGibbon; F A Miles
Journal:  Vision Res       Date:  2006-02-20       Impact factor: 1.886

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