Literature DB >> 10837253

Coherent global motion in the absence of coherent velocity signals.

J Ross1, D R Badcock, A Hayes.   

Abstract

It is widely believed that form and motion are analysed separately in mammalian visual systems. Form is confined within a stream that projects ventrally from V1 to the inferotemporal cortex, and motion within a stream that projects more dorsally, to the posterior parietal cortex [1] [2] [3] [4] [5] [6] [7]. Current descriptions suggest that there is little contact between the two streams until the products of their separate analyses are bound together at a late (and still unidentified) stage in perception [3] [8] [9] [10]. There are, however, indications that form and motion signals may interact [11], and that form signals, streaks derived from motion, may assist in the analysis of its direction [12]. Lennie [13] proposes that all image attributes, form and motion included, remain intimately coupled within the same retinotopic map at all stages of visual analysis. Here we show that form, independent of motion, can give coherence to incoherent motion. Sequences of Glass patterns [14] built to a common global rule are devoid of coherent motion signals, but they produce motion consistent with the global rule for form, not with the random velocity components of the pattern sequence.

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Year:  2000        PMID: 10837253     DOI: 10.1016/s0960-9822(00)00524-8

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


  30 in total

1.  The roles of the convex hull and the number of potential intersections in performance on visually presented traveling salesperson problems.

Authors:  Douglas Vickers; Michael D Lee; Matthew Dry; Peter Hughes
Journal:  Mem Cognit       Date:  2003-10

2.  Direct evidence that "speedlines" influence motion mechanisms.

Authors:  David C Burr; John Ross
Journal:  J Neurosci       Date:  2002-10-01       Impact factor: 6.167

3.  Signals in macaque striate cortical neurons that support the perception of glass patterns.

Authors:  Matthew A Smith; Wyeth Bair; J Anthony Movshon
Journal:  J Neurosci       Date:  2002-09-15       Impact factor: 6.167

4.  Magnocellular contributions to impaired motion processing in schizophrenia.

Authors:  Dongsoo Kim; Glenn Wylie; Roey Pasternak; Pamela D Butler; Daniel C Javitt
Journal:  Schizophr Res       Date:  2005-12-01       Impact factor: 4.939

5.  Glass pattern responses in macaque V2 neurons.

Authors:  Matthew A Smith; Adam Kohn; J Anthony Movshon
Journal:  J Vis       Date:  2007-02-27       Impact factor: 2.240

6.  The dynamic-stimulus advantage of visual symmetry perception.

Authors:  Ryosuke Niimi; Katsumi Watanabe; Kazuhiko Yokosawa
Journal:  Psychol Res       Date:  2008-01-24

7.  Distinct effects of attention on the neural responses to form and motion processing: a SSVEP source-imaging study.

Authors:  Melanie Palomares; Justin M Ales; Alex R Wade; Benoit R Cottereau; Anthony M Norcia
Journal:  J Vis       Date:  2012-09-26       Impact factor: 2.240

8.  Default perception of high-speed motion.

Authors:  Mark Wexler; Andrew Glennerster; Patrick Cavanagh; Hiroyuki Ito; Takeharu Seno
Journal:  Proc Natl Acad Sci U S A       Date:  2013-04-09       Impact factor: 11.205

9.  Apparent speed increases at low luminance.

Authors:  Maryam Vaziri-Pashkam; Patrick Cavanagh
Journal:  J Vis       Date:  2008-12-22       Impact factor: 2.240

10.  MEG responses to the perception of global structure within glass patterns.

Authors:  Jennifer B Swettenham; Stephen J Anderson; Ngoc J Thai
Journal:  PLoS One       Date:  2010-11-05       Impact factor: 3.240

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