Literature DB >> 3153787

Form from motion parallax and form from luminance contrast: vernier discrimination.

D Regan1.   

Abstract

UNLABELLED: Some objects are perfectly camouflaged when stationary, but are clearly visible when moving; the boundaries of such an object are defined entirely by motion parallax. Little is known about the eye's ability to make spatial discriminations between motion-defined objects. In this study, subjects viewed a pseudo-random pattern of dots within which a camouflaged bar was made visible by relative motion of dots. Vernier acuity for the motion-defined bar was 27-45 sec arc for three subjects, much less than the interdot separation of 360 sec arc, much less than the 2 deg receptive field size for motion, and comparable with the foveal intercone separation of 30 sec arc. It is proposed that an opponent-orientation process and an opponent-position process can both contribute to vernier judgements for motion-defined objects. Real-world motion contrast commonly confounds the following cues for figure-ground segregation: (1) different texture velocities on either side of the figure's boundary; (2) in any given time interval, texture in figure and ground moves different distances; and (3) texture continually appears and disappears along the figure's boundary. When cues (2) and (3) were eliminated, thus ensuring figure-ground segregation was achieved entirely by motion-sensitive neural elements, vernier acuity was 44 +/- 5 sec arc compared with 36 +/- 8 sec arc for a dotted bar defined by luminance contrast.
CONCLUSION: Vernier acuity for a dotted bar whose boundary was defined entirely by motion-sensitive neural elements was similar to vernier acuity for a dotted bar whose boundary was defined by luminance contrast.

Mesh:

Year:  1986        PMID: 3153787     DOI: 10.1163/156856886x00106

Source DB:  PubMed          Journal:  Spat Vis        ISSN: 0169-1015


  11 in total

1.  In and out of consciousness: sustained electrophysiological activity reflects individual differences in perceptual awareness.

Authors:  Carson Pun; Stephen M Emrich; Kristin E Wilson; Erene Stergiopoulos; Susanne Ferber
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2.  Single-unit responses to kinetic stimuli in New World monkey area V2: physiological characteristics of cue-invariant neurones.

Authors:  L L Lui; J A Bourne; M G P Rosa
Journal:  Exp Brain Res       Date:  2004-10-23       Impact factor: 1.972

3.  An Orientation Map for Motion Boundaries in Macaque V2.

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Journal:  Cereb Cortex       Date:  2014-09-26       Impact factor: 5.357

4.  Deep tectal cells in pigeons respond to kinematograms.

Authors:  B J Frost; P Cavanagh; B Morgan
Journal:  J Comp Physiol A       Date:  1988-04       Impact factor: 1.836

5.  Processing of motion boundary orientation in macaque V2.

Authors:  Heng Ma; Pengcheng Li; Jiaming Hu; Xingya Cai; Qianling Song; Haidong D Lu
Journal:  Elife       Date:  2021-03-24       Impact factor: 8.140

6.  Local motion processing in the optic tectum of the Japanese toad, Bufo japonicus.

Authors:  M Satou; A Shiraishi
Journal:  J Comp Physiol A       Date:  1991-11       Impact factor: 1.836

7.  Face inversion reduces the persistence of global form and its neural correlates.

Authors:  Lars Strother; Pavagada S Mathuranath; Adrian Aldcroft; Cheryl Lavell; Melvyn A Goodale; Tutis Vilis
Journal:  PLoS One       Date:  2011-04-15       Impact factor: 3.240

8.  Inter-element orientation and distance influence the duration of persistent contour integration.

Authors:  Lars Strother; Danila Alferov
Journal:  Front Psychol       Date:  2014-11-06

9.  Pre-exposure to moving form enhances static form sensitivity.

Authors:  Thomas S A Wallis; Mark A Williams; Derek H Arnold
Journal:  PLoS One       Date:  2009-12-17       Impact factor: 3.240

10.  Visible Persistence of Single-Transient Random Dot Patterns: Spatial Parameters Affect the Duration of Fading Percepts.

Authors:  Maximilian Bruchmann; Kathrin Thaler; Dirk Vorberg
Journal:  PLoS One       Date:  2015-09-08       Impact factor: 3.240

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