Literature DB >> 10393987

The mechanism of isoluminant chromatic motion perception.

Z L Lu1, L A Lesmes, G Sperling.   

Abstract

An isoluminant chromatic display is a color display in which the component colors have been so carefully equated in luminance that they stimulate only color-sensitive perceptual mechanisms and not luminance-sensitive mechanisms. The nature of the mechanism by which isoluminant chromatic motion is perceived is an important issue because color and motion processing historically have been associated with different neural pathways. Here we show that isoluminant chromatic motion (i) fails a pedestal test, (ii) has a temporal tuning function that declines to half-amplitude at 3-6 Hz, and (iii) is perceived equally well when the entire motion sequence is presented monocularly (entire motion sequence to one eye) versus interocularly (the frames of motion sequence alternate between eyes so that neither eye individually could perceive motion). These three characteristics indicate that chromatic motion is detected by the third-order motion system. Based on this theory, it was possible to take a moving isoluminant red-green grating and, by simply increasing the chromatic contrast of the green component, to generate the full gamut of motion percepts, from compelling smooth motion to motion standstill. The perception of motion standstill when the third-order mechanism is nullified indicates that there is no other motion computation available for purely chromatic motion. It follows that isoluminant chromatic motion is not computed by specialized chromatic motion mechanisms within a color pathway but by the third-order motion system at a brain level where binocular inputs of form, color, depth, and texture are simultaneously available and where selective attention can exert a major influence.

Mesh:

Year:  1999        PMID: 10393987      PMCID: PMC22227          DOI: 10.1073/pnas.96.14.8289

Source DB:  PubMed          Journal:  Proc Natl Acad Sci U S A        ISSN: 0027-8424            Impact factor:   11.205


  44 in total

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Journal:  Science       Date:  1988-05-06       Impact factor: 47.728

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Journal:  Vision Res       Date:  1985       Impact factor: 1.886

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Authors:  J Lee; C F Stromeyer
Journal:  J Physiol       Date:  1989-06       Impact factor: 5.182

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  10 in total

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Authors:  T D Albright
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2.  Measuring the amplification of attention.

Authors:  E Blaser; G Sperling; Z L Lu
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3.  Perceptual motion standstill in rapidly moving chromatic displays.

Authors:  Z L Lu; L A Lesmes; G Sperling
Journal:  Proc Natl Acad Sci U S A       Date:  1999-12-21       Impact factor: 11.205

4.  Chromatic sensitivity of neurones in area MT of the anaesthetised macaque monkey compared to human motion perception.

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5.  Motion standstill leads to activation of inferior parietal lobe.

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Journal:  Hum Brain Mapp       Date:  2006-04       Impact factor: 5.038

6.  When motion appears stopped: stereo motion standstill.

Authors:  Chia-huei Tseng; Joetta L Gobell; Zhong-Lin Lu; George Sperling
Journal:  Proc Natl Acad Sci U S A       Date:  2006-09-26       Impact factor: 11.205

7.  Unifying account of visual motion and position perception.

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8.  Human mesenchymal stem cells signals regulate neural stem cell fate.

Authors:  Lianhua Bai; Arnold Caplan; Donald Lennon; Robert H Miller
Journal:  Neurochem Res       Date:  2006-12-27       Impact factor: 3.996

9.  A common framework for the analysis of complex motion? Standstill and capture illusions.

Authors:  Max R Dürsteler
Journal:  Front Hum Neurosci       Date:  2014-12-18       Impact factor: 3.169

10.  Global depth perception alters local timing sensitivity.

Authors:  Nestor Matthews; Leslie Welch; Elena K Festa; Anthony A Bruno; Kendra Schafer
Journal:  PLoS One       Date:  2020-01-23       Impact factor: 3.240

  10 in total

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