scholarly journals Self-motion illusions from distorted optic flow in multifocal glasses

iScience ◽  
2021 ◽  
pp. 103567
Author(s):  
Yannick Sauer ◽  
Malte Scherff ◽  
Markus Lappe ◽  
Katharina Rifai ◽  
Niklas Stein ◽  
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Keyword(s):  
2010 ◽  
Vol 103 (4) ◽  
pp. 1865-1873 ◽  
Author(s):  
Tao Zhang ◽  
Kenneth H. Britten

The ventral intraparietal area (VIP) of the macaque monkey is thought to be involved in judging heading direction based on optic flow. We recorded neuronal discharges in VIP while monkeys were performing a two-alternative, forced-choice heading discrimination task to relate quantitatively the activity of VIP neurons to monkeys' perceptual choices. Most VIP neurons were responsive to simulated heading stimuli and were tuned such that their responses changed across a range of forward trajectories. Using receiver operating characteristic (ROC) analysis, we found that most VIP neurons were less sensitive to small heading changes than was the monkey, although a minority of neurons were equally sensitive. Pursuit eye movements modestly yet significantly increased both neuronal and behavioral thresholds by approximately the same amount. Our results support the view that VIP activity is involved in self-motion judgments.


i-Perception ◽  
2021 ◽  
Vol 12 (6) ◽  
pp. 204166952110557
Author(s):  
Diederick C. Niehorster

The concept of optic flow, a global pattern of visual motion that is both caused by and signals self-motion, is canonically ascribed to James Gibson's 1950 book “ The Perception of the Visual World.” There have, however, been several other developments of this concept, chiefly by Gwilym Grindley and Edward Calvert. Based on rarely referenced scientific literature and archival research, this article describes the development of the concept of optic flow by the aforementioned authors and several others. The article furthermore presents the available evidence for interactions between these authors, focusing on whether parts of Gibson's proposal were derived from the work of Grindley or Calvert. While Grindley's work may have made Gibson aware of the geometrical facts of optic flow, Gibson's work is not derivative of Grindley's. It is furthermore shown that Gibson only learned of Calvert's work in 1956, almost a decade after Gibson first published his proposal. In conclusion, the development of the concept of optic flow presents an intriguing example of convergent thought in the progress of science.


2017 ◽  
Vol 17 (10) ◽  
pp. 211
Author(s):  
Jonathan Matthis ◽  
Karl Muller ◽  
Kathryn Bonnen ◽  
Mary Hayhoe

2020 ◽  
Vol 117 (27) ◽  
pp. 16065-16071 ◽  
Author(s):  
Yuli Wu ◽  
Kepu Chen ◽  
Yuting Ye ◽  
Tao Zhang ◽  
Wen Zhou

Human navigation relies on inputs to our paired eyes and ears. Although we also have two nasal passages, there has been little empirical indication that internostril differences yield directionality in human olfaction without involving the trigeminal system. By using optic flow that captures the pattern of apparent motion of surface elements in a visual scene, we demonstrate through formal psychophysical testing that a moderate binaral concentration disparity of a nontrigeminal odorant consistently biases recipients’ perceived direction of self-motion toward the higher-concentration side, despite that they cannot verbalize which nostril smells a stronger odor. We further show that the effect depends on the internostril ratio of odor concentrations and not the numeric difference in concentration between the two nostrils. Taken together, our findings provide behavioral evidence that humans smell in stereo and subconsciously utilize stereo olfactory cues in spatial navigation.


1998 ◽  
Vol 79 (3) ◽  
pp. 1461-1480 ◽  
Author(s):  
Markus Lappe ◽  
Martin Pekel ◽  
Klaus-Peter Hoffmann

Lappe, Markus, Martin Pekel, and Klaus-Peter Hoffmann. Optokinetic eye movements elicited by radial optic flow in the macaque monkey. J. Neurophysiol. 79: 1461–1480, 1998. We recorded spontaneous eye movements elicited by radial optic flow in three macaque monkeys using the scleral search coil technique. Computer-generated stimuli simulated forward or backward motion of the monkey with respect to a number of small illuminated dots arranged on a virtual ground plane. We wanted to see whether optokinetic eye movements are induced by radial optic flow stimuli that simulate self-movement, quantify their parameters, and consider their effects on the processing of optic flow. A regular pattern of interchanging fast and slow eye movements with a frequency of 2 Hz was observed. When we shifted the horizontal position of the focus of expansion (FOE) during simulated forward motion (expansional optic flow), median horizontal eye position also shifted in the same direction but only by a smaller amount; for simulated backward motion (contractional optic flow), median eye position shifted in the opposite direction. We relate this to a change in Schlagfeld typically observed in optokinetic nystagmus. Direction and speed of slow phase eye movements were compared with the local flow field motion in gaze direction (the foveal flow). Eye movement direction matched well the foveal motion. Small systematic deviations could be attributed to an integration of the global motion pattern. Eye speed on average did not match foveal stimulus speed, as the median gain was only ∼0.5–0.6. The gain was always lower for expanding than for contracting stimuli. We analyzed the time course of the eye movement immediately after each saccade. We found remarkable differences in the initial development of gain and directional following for expansion and contraction. For expansion, directional following and gain were initially poor and strongly influenced by the ongoing eye movement before the saccade. This was not the case for contraction. These differences also can be linked to properties of the optokinetic system. We conclude that optokinetic eye movements can be elicited by radial optic flow fields simulating self-motion. These eye movements are linked to the parafoveal flow field, i.e., the motion in the direction of gaze. In the retinal projection of the optic flow, such eye movements superimpose retinal slip. This results in complex retinal motion patterns, especially because the gain of the eye movement is small and variable. This observation has special relevance for mechanisms that determine self-motion from retinal flow fields. It is necessary to consider the influence of eye movements in optic flow analysis, but our results suggest that direction and speed of an eye movement should be treated differently.


2019 ◽  
Vol 32 (3) ◽  
pp. 165-178 ◽  
Author(s):  
Mathieu Koppen ◽  
Arjan C. ter Horst ◽  
W. Pieter Medendorp

Abstract When walking or driving, it is of the utmost importance to continuously track the spatial relationship between objects in the environment and the moving body in order to prevent collisions. Although this process of spatial updating occurs naturally, it involves the processing of a myriad of noisy and ambiguous sensory signals. Here, using a psychometric approach, we investigated the integration of visual optic flow and vestibular cues in spatially updating a remembered target position during a linear displacement of the body. Participants were seated on a linear sled, immersed in a stereoscopic virtual reality environment. They had to remember the position of a target, briefly presented before a sideward translation of the body involving supra-threshold vestibular cues and whole-field optic flow that provided slightly discrepant motion information. After the motion, using a forced response participants indicated whether the location of a brief visual probe was left or right of the remembered target position. Our results show that in a spatial updating task involving passive linear self-motion humans integrate optic flow and vestibular self-displacement information according to a weighted-averaging process with, across subjects, on average about four times as much weight assigned to the visual compared to the vestibular contribution (i.e., 79% visual weight). We discuss our findings with respect to previous literature on the effect of optic flow on spatial updating performance.


2009 ◽  
Vol 102 (6) ◽  
pp. 3606-3618 ◽  
Author(s):  
Kit D. Longden ◽  
Holger G. Krapp

Active locomotive states are metabolically expensive and require efficient sensory processing both to avoid wasteful movements and to cope with an extended bandwidth of sensory stimuli. This is particularly true for flying animals because flight, as opposed to walking or resting, imposes a steplike increase in metabolism for the precise execution and control of movements. Sensory processing itself carries a significant metabolic cost, but the principles governing the adjustment of sensory processing to different locomotor states are not well understood. We use the blowfly as a model system to study the impact on visual processing of a neuromodulator, octopamine, which is known to be involved in the regulation of flight physiology. We applied an octopamine agonist and recorded the directional motion responses of identified visual interneurons known to process self-motion–induced optic flow to directional motion stimuli. The neural response range of these neurons is increased and the response latency is reduced. We also found that, due to an elevated spontaneous spike rate, the cells' negative signaling range is increased. Meanwhile, the preferred self-motion parameters the cells encode were state independent. Our results indicate that in the blowfly energetically expensive sensory coding strategies, such as rapid, large responses, and high spontaneous spike activity could be adjusted by the neuromodulator octopamine, likely to save energy during quiet locomotor states.


2014 ◽  
Vol 10 (5) ◽  
pp. 20140279 ◽  
Author(s):  
Christine Scholtyssek ◽  
Marie Dacke ◽  
Ronald Kröger ◽  
Emily Baird

To detect and avoid collisions, animals need to perceive and control the distance and the speed with which they are moving relative to obstacles. This is especially challenging for swimming and flying animals that must control movement in a dynamic fluid without reference from physical contact to the ground. Flying animals primarily rely on optic flow to control flight speed and distance to obstacles. Here, we investigate whether swimming animals use similar strategies for self-motion control to flying animals by directly comparing the trajectories of zebrafish ( Danio rerio ) and bumblebees ( Bombus terrestris ) moving through the same experimental tunnel. While moving through the tunnel, black and white patterns produced (i) strong horizontal optic flow cues on both walls, (ii) weak horizontal optic flow cues on both walls and (iii) strong optic flow cues on one wall and weak optic flow cues on the other. We find that the mean speed of zebrafish does not depend on the amount of optic flow perceived from the walls. We further show that zebrafish, unlike bumblebees, move closer to the wall that provides the strongest visual feedback. This unexpected preference for strong optic flow cues may reflect an adaptation for self-motion control in water or in environments where visibility is limited.


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.


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