How the visual system extracts surface slant from optic flow

1994 ◽  
Vol 14 (4) ◽  
pp. 440
Author(s):  
T Freeman
2017 ◽  
Vol 27 (21) ◽  
pp. 3225-3236.e3 ◽  
Author(s):  
Kit D. Longden ◽  
Martina Wicklein ◽  
Ben J. Hardcastle ◽  
Stephen J. Huston ◽  
Holger G. Krapp
Keyword(s):  

2020 ◽  
Vol 117 (52) ◽  
pp. 33161-33169
Author(s):  
Charlie S. Burlingham ◽  
David J. Heeger

There is considerable support for the hypothesis that perception of heading in the presence of rotation is mediated by instantaneous optic flow. This hypothesis, however, has never been tested. We introduce a method, termed “nonvarying phase motion,” for generating a stimulus that conveys a single instantaneous optic flow field, even though the stimulus is presented for an extended period of time. In this experiment, observers viewed stimulus videos and performed a forced-choice heading discrimination task. For nonvarying phase motion, observers made large errors in heading judgments. This suggests that instantaneous optic flow is insufficient for heading perception in the presence of rotation. These errors were mostly eliminated when the velocity of phase motion was varied over time to convey the evolving sequence of optic flow fields corresponding to a particular heading. This demonstrates that heading perception in the presence of rotation relies on the time-varying evolution of optic flow. We hypothesize that the visual system accurately computes heading, despite rotation, based on optic acceleration, the temporal derivative of optic flow.


Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 61-61
Author(s):  
A Grigo ◽  
M Lappe

We investigated the influence of stereoscopic vision on the perception of optic flow fields in psychophysical experiments based on the effect of an illusory transformation found by Duffy and Wurtz (1993 Vision Research33 1481 – 1490). Human subjects are not able to determine the centre of an expanding optic flow field correctly if the expansion is transparently superimposed on a unidirectional motion pattern. Its location is rather perceived shifted in the direction of the translational movement. Duffy and Wurtz proposed that this illusory shift is caused by the visual system taking the presented flow pattern as a flow field composed of linear self-motion and an eye rotation. As a consequence, the centre of the expansional movement is determined by compensating for the simulated eye rotation, like determining one's direction of heading (Lappe and Rauschecker, 1994 Vision Research35 1619 – 1631). In our experiments we examined the dependence of the illusory transformation on differences in depth between the superimposed movements. We presented the expansional and translational stimuli with different relative binocular disparities. In the case of zero disparity, we could confirm the results of Duffy and Wurtz. For uncrossed disparities (ie translation behind expansion) we found a small and nonsignificant decrease of the illusory shift. In contrast, there was a strong decrease up to 80% in the case of crossed disparity (ie translation in front of expansion). These findings confirm the assumption that the motion pattern is interpreted as a self-motion flow field: only in the unrealistic case of a large rotational component present in front of an expansion are the superimposed movements interpreted separately by the visual system.


As a basis for understanding the visual system, we need to consider the functions that vision has to perform, which are pre-eminently in the service of activity, and the circumstances in which it normally operates, namely when the head is moving. The fundamental ecological stimulus for vision is not a camera-like time-frozen image but a constantly changing optic array or flow field, the description of which must be in spatio-temporal terms. A mathematical analysis of the optic flow field is presented, revealing the information that it affords for controlling activity - information both about the topography of the environment and about the movement of the organism relative to the environment. Results of human behavioural experiments are also reported. It is suggested that the optic flow field should be the starting point in attempting to discover the physiological workings of the visual system.


Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 50-50
Author(s):  
T C A Freeman ◽  
T S Meese ◽  
M G Harris

A growing body of evidence suggests that optic flow is processed by specialised 2-D motion mechanisms. We asked whether the visual system has parallel, or rapid serial, access to representations of optic flow components in a spatial 4AFC task. Random-dot kinematograms (144 dots per interval) depicting expansion, rotation, deformation (horizontal shear+vertical shear) or one of these components summed with translation, were presented in four spatially abutting circular windows (2.65 deg in diameter), and were temporally modulated by half a cycle of a 300 ms cosine-wave. Within a session, stimuli were of the same type, but the target had opposite sign and was selected with a mouse and cursor with feedback. Systematic local cues were removed by randomising (i) the orientation of the windowing configuration, and (ii) the dot speeds between intervals (speed gradient varied between 2.4% and 6%; translation varied between 16 and 40 min arc s−1). Preliminary results (average SE=3.4%) showed that in the absence of translation, performance was close to chance (25% correct) for rotation (23% correct) and deformation (27% correct), but was good for expansion (61% correct). The addition of translation had no effect on rotation but improved deformation (58% correct) and impaired expansion (22% correct). In experiment 2, unlimited stimulus repetitions were allowed and performance improved (>93%) for all conditions, though, as predicted from experiment 1, reaction times were fastest for expansion and deformation-plus-translation. Importantly, only these two conditions produced unambiguous 3-D perceptions of the stimuli, suggesting that surface slant and motion in depth are coded by mechanisms more rapidly accessible than those subserving general extraction of 2-D motion.


2011 ◽  
Vol 214 (9) ◽  
pp. 1586-1598 ◽  
Author(s):  
B. G. Horseman ◽  
M. W. S. Macauley ◽  
W. J. P. Barnes

2012 ◽  
Vol 107 (12) ◽  
pp. 3446-3457 ◽  
Author(s):  
Pei Liang ◽  
Jochen Heitwerth ◽  
Roland Kern ◽  
Rafael Kurtz ◽  
Martin Egelhaaf

Three motion-sensitive key elements of a neural circuit, presumably involved in processing object and distance information, were analyzed with optic flow sequences as experienced by blowflies in a three-dimensional environment. This optic flow is largely shaped by the blowfly's saccadic flight and gaze strategy, which separates translational flight segments from fast saccadic rotations. By modifying this naturalistic optic flow, all three analyzed neurons could be shown to respond during the intersaccadic intervals not only to nearby objects but also to changes in the distance to background structures. In the presence of strong background motion, the three types of neuron differ in their sensitivity for object motion. Object-induced response increments are largest in FD1, a neuron long known to respond better to moving objects than to spatially extended motion patterns, but weakest in VCH, a neuron that integrates wide-field motion from both eyes and, by inhibiting the FD1 cell, is responsible for its object preference. Small but significant object-induced response increments are present in HS cells, which serve both as a major input neuron of VCH and as output neurons of the visual system. In both HS and FD1, intersaccadic background responses decrease with increasing distance to the animal, although much more prominently in FD1. This strong dependence of FD1 on background distance is concluded to be the consequence of the activity of VCH that dramatically increases its activity and, thus, its inhibitory strength with increasing distance.


PLoS ONE ◽  
2011 ◽  
Vol 6 (4) ◽  
pp. e18731 ◽  
Author(s):  
Corrado Caudek ◽  
Carlo Fantoni ◽  
Fulvio Domini

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