THESIS
2018
xxi, 217 pages : illustrations (some color) ; 30 cm
Abstract
Visually induced motion sickness (VIMS) is a response commonly reported by viewers exposing
to visual stimulation that can provoke self-motion perception (vection). The VIMS susceptibility
(VIMSS) varies largely in the population and the neural mechanism for the variation is still
unclear. Based on the sensory conflict theory, VIMSS depends on the ability to regulate visual
response and coordinate self-motion information between visual and extra-visual modalities
under vection-inducing stimulation. However, those hypotheses have not yet been systematically
tested. To bridge current research gaps, we need to identify new behavioral and neurological
covariates for both vection and VIMSS. In particular, we need indicators that: 1) are of higher
time resolution; 2) can reflect the d...[
Read more ]
Visually induced motion sickness (VIMS) is a response commonly reported by viewers exposing
to visual stimulation that can provoke self-motion perception (vection). The VIMS susceptibility
(VIMSS) varies largely in the population and the neural mechanism for the variation is still
unclear. Based on the sensory conflict theory, VIMSS depends on the ability to regulate visual
response and coordinate self-motion information between visual and extra-visual modalities
under vection-inducing stimulation. However, those hypotheses have not yet been systematically
tested. To bridge current research gaps, we need to identify new behavioral and neurological
covariates for both vection and VIMSS. In particular, we need indicators that: 1) are of higher
time resolution; 2) can reflect the difference of central and peripheral vision; and 3) can reflect
information coordination between visual and extra-visual modalities. This research comprises four studies to explore both behavioral task performances and electroencephalography (EEG)
signatures that correlate with vection qualitatively (assess the existence of vection) and
quantitatively (assess the magnitude of vection intensity). Study one discovered that under
vection, the visual performance of sustained attention to response task (SART) is impaired in
central vision and strengthened in peripheral vision to facilitate the processing of self-motion
cues. Study two examined the temporal characteristics of transient visually evoked potentials
(VEP) from central visual field under the same peripheral vection-inducing stimulation. Results
suggest that earlier VEP components are more closely associated with vection perception than
VEP components observed later (>350ms). Study three examined the more stable steady-state
VEP with frequency tags at central and peripheral visual field to explore more reliable indicators
along with the spatial properties of effects. Results revealed a shift of visual information
processing emphasis from occipital to parietal under vection. Study four investigated the phase
synchrony between visual and extra-visual regions. Results suggest the information coordination
between parietal regions and other widely distributed regions are strengthened under vection-inducing
stimulation. Furthermore, the magnitudes of those vection associated effects are
negatively associated with the VIMSS of participants, hence, can serve as indicators to
differentiate VIMS susceptible and resistant groups: the more people are resistant to VIMS, the
stronger are the vection effects. In general, our findings support the sensory conflict theory from
the perspective of individual differences. Identified behavioral and EEG signatures can contribute
to not only the better understanding of VIMS, but also the development of new objective vection
measures and VIMS predictors.
Post a Comment