scholarly journals Optic flow in human vision: MEG reveals a foveo-fugal bias in V1, specialization for spiral space in hMSTs, and global motion sensitivity in the IPS

2008 ◽  
Vol 8 (10) ◽  
pp. 17-17 ◽  
Author(s):  
I. E. Holliday ◽  
T. S. Meese
2008 ◽  
Vol 25 (5-6) ◽  
pp. 675-684 ◽  
Author(s):  
CYNTHIA HALL-HARO ◽  
LYNNE KIORPES

AbstractWe studied the development of sensitivity to complex motion using plaid patterns. We hypothesized, based on neurophysiological data showing a dearth of pattern direction–selective (PDS) cells in area medial temporal (MT) of infant macaques, that sensitivity to pattern motion would develop later than other forms of global motion sensitivity. We tested 10 macaque monkeys (Macaca nemestrina) ranging in age from 7 weeks to 109–160 weeks (adult). The monkeys discriminated horizontal from vertical pattern motion; sensitivity for one-dimensional (1D) direction discrimination and detection were tested as control tasks. The results show that pattern motion discrimination ability develops relatively late, between 10 and 18 weeks, while performance on the 1D control tasks was excellent at the earliest test ages. Plaid discrimination performance depends on both the speed and spatial scale of the underlying patterns. However, development is not limited by contrast sensitivity. These results support the idea that pattern motion perception depends on a different mechanism than other forms of global motion perception and are consistent with the idea that the representation of PDS neurons in MT may limit the development of complex motion perception.


Cephalalgia ◽  
2006 ◽  
Vol 26 (8) ◽  
pp. 949-959 ◽  
Author(s):  
AM McKendrick ◽  
A Turpin ◽  
S Webb ◽  
DR Badcock

Some migraineurs have increased thresholds for the detection of global dot motion. We investigated whether migraineurs show consequential abnormalities in the determination of direction of self-motion (heading) from simulated optic flow. The ability to determine heading from optic flow is likely to be necessary for optimal determination of self-motion through the environment. Twenty-five migraineurs and 25 controls participated. Global dot motion coherence thresholds were assessed, in addition to performance on two simulated heading tasks: one with a symmetrical flow field, and the second with differing velocity of optic flow on the left and right sides of the participant. While some migraineurs demonstrated abnormal global motion coherence thresholds, there was no difference in performance on the heading tasks at either simulated walking (5 km/h) or driving (50 km/h) speeds. Increased global motion coherence thresholds in migraineurs do not result in abnormal judgements of heading from 100± coherent optic flow.


2021 ◽  
Vol 15 ◽  
Author(s):  
Serena Micheletti ◽  
Fleur Corbett ◽  
Janette Atkinson ◽  
Oliver Braddick ◽  
Paola Mattei ◽  
...  

Dorsal stream cortical networks underpin a cluster of visuomotor, visuospatial, and visual attention functions. Sensitivity to global coherence of motion and static form is considered a signature of visual cortical processing in the dorsal stream (motion) relative to the ventral stream (form). Poorer sensitivity to global motion compared to global static form has been found across a diverse range of neurodevelopmental disorders, suggesting a “dorsal stream vulnerability.” However, previous studies of global coherence sensitivity in Developmental Coordination Disorder (DCD) have shown conflicting findings. We examined two groups totalling 102 children with DCD (age 5–12 years), using the “Ball in the Grass” psychophysical test to compare sensitivity to global motion and global static form. Motor impairment was measured using the Movement-ABC (M-ABC). Global coherence sensitivity was compared with a typically developing control group (N = 69) in the same age range. Children with DCD showed impaired sensitivity to global motion (p = 0.002), but not global form (p = 0.695), compared to controls. Within the DCD group, motor impairment showed a significant linear relationship with global form sensitivity (p < 0.001). There was also a significant quadratic relationship between motor impairment and global motion sensitivity (p = 0.046), where poorer global motion sensitivity was only apparent with greater motor impairment. We suggest that two distinct visually related components, associated with global form and global motion sensitivity, contribute to DCD differentially over the range of severity of the disorder. Possible neural circuitry underlying these relationships is discussed.


2011 ◽  
Vol 51 (3) ◽  
pp. 352-361 ◽  
Author(s):  
Carlos R. Cassanello ◽  
Mark Edwards ◽  
David R. Badcock ◽  
Shin’ya Nishida

Vision ◽  
2019 ◽  
Vol 3 (2) ◽  
pp. 13
Author(s):  
Pearl Guterman ◽  
Robert Allison

When the head is tilted, an objectively vertical line viewed in isolation is typically perceived as tilted. We explored whether this shift also occurs when viewing global motion displays perceived as either object-motion or self-motion. Observers stood and lay left side down while viewing (1) a static line, (2) a random-dot display of 2-D (planar) motion or (3) a random-dot display of 3-D (volumetric) global motion. On each trial, the line orientation or motion direction were tilted from the gravitational vertical and observers indicated whether the tilt was clockwise or counter-clockwise from the perceived vertical. Psychometric functions were fit to the data and shifts in the point of subjective verticality (PSV) were measured. When the whole body was tilted, the perceived tilt of both a static line and the direction of optic flow were biased in the direction of the body tilt, demonstrating the so-called A-effect. However, we found significantly larger shifts for the static line than volumetric global motion as well as larger shifts for volumetric displays than planar displays. The A-effect was larger when the motion was experienced as self-motion compared to when it was experienced as object-motion. Discrimination thresholds were also more precise in the self-motion compared to object-motion conditions. Different magnitude A-effects for the line and motion conditions—and for object and self-motion—may be due to differences in combining of idiotropic (body) and vestibular signals, particularly so in the case of vection which occurs despite visual-vestibular conflict.


2017 ◽  
Vol 30 (7-8) ◽  
pp. 739-761 ◽  
Author(s):  
Ramy Kirollos ◽  
Robert S. Allison ◽  
Stephen Palmisano

Behavioural studies have consistently found stronger vection responses for oscillating, compared to smooth/constant, patterns of radial flow (the simulated viewpoint oscillation advantage for vection). Traditional accounts predict that simulated viewpoint oscillation should impair vection by increasing visual–vestibular conflicts in stationary observers (as this visual oscillation simulates self-accelerations that should strongly stimulate the vestibular apparatus). However, support for increased vestibular activity during accelerating vection has been mixed in the brain imaging literature. This fMRI study examined BOLD activity in visual (cingulate sulcus visual area — CSv; medial temporal complex — MT+; V6; precuneus motion area — PcM) and vestibular regions (parieto-insular vestibular cortex — PIVC/posterior insular cortex — PIC; ventral intraparietal region — VIP) when stationary observers were exposed to vection-inducing optic flow (i.e., globally coherent oscillating and smooth self-motion displays) as well as two suitable control displays. In line with earlier studies in which no vection occurred, CSv and PIVC/PIC both showed significantly increased BOLD activity during oscillating global motion compared to the other motion conditions (although this effect was found for fewer subjects in PIVC/PIC). The increase in BOLD activity in PIVC/PIC during prolonged exposure to the oscillating (compared to smooth) patterns of global optical flow appears consistent with vestibular facilitation.


2013 ◽  
Vol 84 ◽  
pp. 16-25 ◽  
Author(s):  
Claire V. Hutchinson ◽  
Tim Ledgeway ◽  
Harriet A. Allen ◽  
Mike D. Long ◽  
Amanda Arena

2016 ◽  
Vol 28 (12) ◽  
pp. 1897-1908 ◽  
Author(s):  
Oliver Braddick ◽  
Janette Atkinson ◽  
Erik Newman ◽  
Natacha Akshoomoff ◽  
Joshua M. Kuperman ◽  
...  

Sensitivity to global visual motion has been proposed as a signature of brain development, related to the dorsal rather than ventral cortical stream. Thresholds for global motion have been found to be elevated more than for global static form in many developmental disorders, leading to the idea of “dorsal stream vulnerability.” Here we explore the association of global motion thresholds with individual differences in children's brain development, in a group of typically developing 5- to 12-year-olds. Good performance was associated with a relative increase in parietal lobe surface area, most strongly around the intraparietal sulcus and decrease in occipital area. In line with the involvement of intraparietal sulcus, areas in visuospatial and numerical cognition, we also found that global motion performance was correlated with tests of visuomotor integration and numerical skills. Individual differences in global form detection showed none of these anatomical or cognitive correlations. This suggests that the correlations with motion sensitivity are unlikely to reflect general perceptual or attentional abilities required for both form and motion. We conclude that individual developmental variations in global motion processing are not linked to greater area in the extrastriate visual areas, which initially process such motion, but in the parietal systems that make decisions based on this information. The overlap with visuospatial and numerical abilities may indicate the anatomical substrate of the “dorsal stream vulnerability” proposed as characterizing neurodevelopmental disorders.


2012 ◽  
Vol 68 ◽  
pp. 28-39 ◽  
Author(s):  
Craig Aaen-Stockdale ◽  
Timothy Ledgeway ◽  
Paul McGraw ◽  
Robert F. Hess

Sign in / Sign up

Export Citation Format

Share Document