Literature DB >> 18818907

Positional and directional preponderances in vection.

Takeharu Seno1, Takao Sato.   

Abstract

We examined the biases in vection strength caused by motion direction (temporonasal vs. nasotemporal motion) and position of stimulus presentation (nasal and temporal semi-retinas) to investigate a subcortical contribution to vection. These biases have been identified for optokinetic nystagmus (OKN) and are acknowledged as evidence for a subcortical origin of OKN. In experiments, subjects monocularly observed hemi-field motion stimuli and made magnitude estimations. The results indicated significant directional and positional biases when luminance modulated gratings were used as stimuli. Vection was stronger with nasotemporal motions and nasal retina presentations, but there were no interactions between the two factors. However, these biases disappeared for second-order motion stimuli (contrast modulation), which are presumably processed by the cortex. In addition, when subjects were asked to make subjective ratings of motion impression, there was no significant difference in subjective strength between the stimuli that induced the strongest vection and weakest vection. These results, together, suggest the involvement of the subcortical pathway in vection induction.

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Year:  2008        PMID: 18818907     DOI: 10.1007/s00221-008-1575-6

Source DB:  PubMed          Journal:  Exp Brain Res        ISSN: 0014-4819            Impact factor:   1.972


  28 in total

1.  Directional asymmetry of neurons in cortical areas MT and MST projecting to the NOT-DTN in macaques.

Authors:  K-P Hoffmann; F Bremmer; A Thiele; C Distler
Journal:  J Neurophysiol       Date:  2002-04       Impact factor: 2.714

2.  Effects of spatial arrangement of visual stimulus on inverted self-motion perception induced by the foreground motion: examination of OKN-suppression hypothesis.

Authors:  Shinji Nakamura
Journal:  Vision Res       Date:  2004       Impact factor: 1.886

3.  Reciprocal inhibitory visual-vestibular interaction. Visual motion stimulation deactivates the parieto-insular vestibular cortex.

Authors:  T Brandt; P Bartenstein; A Janek; M Dieterich
Journal:  Brain       Date:  1998-09       Impact factor: 13.501

4.  Optokinetic nystagmus: the effects of stationary edges, alone and in combination with central occlusion.

Authors:  C M Murasugi; I P Howard; M Ohmi
Journal:  Vision Res       Date:  1986       Impact factor: 1.886

5.  The termination of retinal axons in the pretectal region of mammals.

Authors:  F Scalia
Journal:  J Comp Neurol       Date:  1972-06       Impact factor: 3.215

6.  Optokinetic eye movements in the rabbit: input-output relations.

Authors:  H Collewijn
Journal:  Vision Res       Date:  1969-01       Impact factor: 1.886

7.  The cerebral activity related to the visual perception of forward motion in depth.

Authors:  B M de Jong; S Shipp; B Skidmore; R S Frackowiak; S Zeki
Journal:  Brain       Date:  1994-10       Impact factor: 13.501

8.  Motion defined exclusively by second-order characteristics does not evoke optokinetic nystagmus.

Authors:  L R Harris; A T Smith
Journal:  Vis Neurosci       Date:  1992-12       Impact factor: 3.241

9.  Optokinetic and vection responses to apparent motion in man.

Authors:  C M Schor; V Lakshminarayanan; V Narayan
Journal:  Vision Res       Date:  1984       Impact factor: 1.886

10.  Neural correlates of visual-motion perception as object- or self-motion.

Authors:  Andreas Kleinschmidt; Kai V Thilo; Christian Büchel; Michael A Gresty; Adolfo M Bronstein; Richard S J Frackowiak
Journal:  Neuroimage       Date:  2002-08       Impact factor: 6.556

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  1 in total

1.  Larger Head Displacement to Optic Flow Presented in the Lower Visual Field.

Authors:  Kanon Fujimoto; Hiroshi Ashida
Journal:  Iperception       Date:  2019-11-22
  1 in total

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