Influences of Motion and Depth on Brightness Induction: An Illusory Transparency Effect?

Perception ◽  
10.1068/p3439 ◽  
2002 ◽  
Vol 31 (12) ◽  
pp. 1449-1457 ◽  
Author(s):  
Kazunori Morikawa ◽  
Thomas V Papathomas

Two experiments were performed to investigate whether motion and binocular disparity influence brightness induction, and whether the effects of motion and binocular disparity, if any, interact with each other. In order to introduce motion, textured backgrounds were used as the inducing field. The results showed that motion and/or crossed disparity reduce brightness induction, whereas uncrossed disparity increases it. The effect of motion and the effect of disparity are independent of each other and additive, which suggests that, to the extent that brightness induction reflects segmentation of objects, motion and binocular disparity serve independently to segment objects from their background. The difference between the effects of crossed and uncrossed disparity can be explained by what we call ‘illusory transparency’.

2021 ◽  
Author(s):  
Ryan Edward O'Donnell ◽  
Kyrie Murawski ◽  
Ella Herrmann ◽  
Jesse Wisch ◽  
Garrett D. Sullivan ◽  
...  

There have been conflicting findings on the degree to which exogenous/reflexive visual attention is selective for depth, and this issue has important implications for attention models. Previous findings have attempted to find depth-based cueing effects on such attention using reaction time measures for stimuli presented in stereo goggles with a display screen. Results stemming from such approaches have been mixed, depending on whether target/distractor discrimination was required. To help clarify the existence of such depth effects, we have developed a paradigm that measures accuracy rather than reaction time in an immersive virtual-reality environment, providing a more appropriate context of depth. Four modified Posner Cueing paradigms were run to test for depth-specific attentional selectivity. Participants fixated a cross while attempting to identify a rapidly masked letter that was preceded by a cue that could be valid in depth and side, depth only, or side only. In Experiment 1, a potent cueing effect was found for side validity and a weak effect was found for depth. Experiment 2 controlled for differences in cue and target sizes when presented at different depths, which caused the depth validity effect to disappear entirely even though participants were explicitly asked to report depth and the difference in virtual depth was extreme (20 vs 300 meters). Experiments 3a and 3b brought the front depth plane even closer (1 m) to maximize effects of binocular disparity, but no reliable depth cueing validity was observed. Thus, it seems that rapid/exogenous attention pancakes 3-dimensional space into a 2-dimensional reference frame.


2015 ◽  
Vol 113 (5) ◽  
pp. 1545-1555 ◽  
Author(s):  
Douglas A. Ruff ◽  
Richard T. Born

Attending to a stimulus modulates the responses of sensory neurons that represent features of that stimulus, a phenomenon named “feature attention.” For example, attending to a stimulus containing upward motion enhances the responses of upward-preferring direction-selective neurons in the middle temporal area (MT) and suppresses the responses of downward-preferring neurons, even when the attended stimulus is outside of the spatial receptive fields of the recorded neurons (Treue S, Martinez-Trujillo JC. Nature 399: 575–579, 1999). This modulation renders the representation of sensory information across a neuronal population more selective for the features present in the attended stimulus (Martinez-Trujillo JC, Treue S. Curr Biol 14: 744–751, 2004). We hypothesized that if feature attention modulates neurons according to their tuning preferences, it should also be sensitive to their tuning strength, which is the magnitude of the difference in responses to preferred and null stimuli. We measured how the effects of feature attention on MT neurons in rhesus monkeys ( Macaca mulatta) depended on the relationship between features—in our case, direction of motion and binocular disparity—of the attended stimulus and a neuron's tuning for those features. We found that, as for direction, attention to stimuli containing binocular disparity cues modulated the responses of MT neurons and that the magnitude of the modulation depended on both a neuron's tuning preferences and its tuning strength. Our results suggest that modulation by feature attention may depend not just on which features a neuron represents but also on how well the neuron represents those features.


Perception ◽  
1974 ◽  
Vol 3 (2) ◽  
pp. 153-168 ◽  
Author(s):  
S M Anstis ◽  
J P Harris

Five subjects adapted for 30 min to a textured disc lying in front of the fixation point with 0·1 deg(1) crossed disparity, which rotated clockwise at 4 rev/min, alternating with a disc behind the fixation point, with 0·1 deg of arc uncrossed disparity, which rotated anticlockwise. A stationary test field then appeared to rotate anticlockwise when it lay in front of the fixation point, and clockwise when it lay behind. Conversely, a test field in the plane of fixation briefly appeared to lie a few millimetres behind the fixation plane when it rotated clockwise, and in front when it rotated anticlockwise. The movement aftereffect contingent on disparity reappeared each time the test disparity was reversed, but the total duration of each successive aftereffect in the series decreased exponentially with elapsed time. Movement aftereffects contingent on disparity were very much stronger than those contingent on colour and won out over them when disparity was pitted against colour.


Author(s):  
Woodrow Barfield ◽  
Craig Rosenberg

The purpose of this study was to investigate the use of three-dimensional display formats for judgments of spatial information using an exocentric frame of reference. Eight subjects judged the azimuth and elevation that separated two computer-generated objects using either a perspective or stereoscopic display. Errors, which consisted of the difference in absolute value between the estimated and actual azimuth or elevation, were analyzed as the response variable. The data indicated that the stereoscopic display resulted in more accurate estimates of elevation, especially for images aligned approximately orthogonally to the viewing vector. However, estimates of relative azimuth direction were not improved by use of the stereoscopic display. Furthermore, it was shown that the effect of compression resulting from a 45--deg computer graphics eye point elevation produced a response bias that was symmetrical around the horizontal plane of the reference cube, and that the depth cue of binocular disparity provided by the stereoscopic display reduced the magnitude of the compression errors. Implications of the results for the design of spatial displays are discussed.


2019 ◽  
Author(s):  
Alessandro La Chioma ◽  
Tobias Bonhoeffer ◽  
Mark Hübener

SummaryBinocular disparity, the difference between left and right eye images, is a powerful cue for depth perception. Many neurons in the visual cortex of higher mammals are sensitive to binocular disparity, with distinct disparity tuning properties across primary and higher visual areas. Mouse primary visual cortex (V1) has been shown to contain disparity-tuned neurons, but it is unknown how these signals are processed beyond V1. We find that disparity signals are prominent in higher areas of mouse visual cortex. Preferred disparities markedly differ among visual areas, with area RL encoding visual stimuli very close to the mouse. Moreover, disparity preference is systematically related to visual field elevation, such that neurons with receptive fields in the lower visual field are overall tuned to near disparities, likely reflecting an adaptation to natural image statistics. Our results reveal ecologically relevant areal specializations for binocular disparity processing across mouse visual cortex.


2020 ◽  
Author(s):  
Alessandro La Chioma ◽  
Tobias Bonhoeffer ◽  
Mark Hübener

AbstractBinocular disparity, the difference between the two eyes’ images, is a powerful cue to generate the three-dimensional depth percept known as stereopsis. In primates, binocular disparity is processed in multiple areas of the visual cortex, with distinct contributions of higher areas to specific aspects of depth perception. Mice, too, can perceive stereoscopic depth, and neurons in primary visual cortex (V1) and higher-order, lateromedial (LM) and rostrolateral (RL) areas were found to be sensitive to binocular disparity. A detailed characterization of disparity tuning properties across mouse visual areas is lacking, however, and acquiring such data might help clarifying the role of higher areas for disparity processing and establishing putative functional correspondences to primate areas. We used two-photon calcium imaging to characterize the disparity tuning properties of neurons in mouse visual areas V1, LM, and RL in response to dichoptically presented binocular gratings, as well as correlated and anticorrelated random dot stereograms (RDS). In all three areas, many neurons were tuned to disparity, showing strong response facilitation or suppression at optimal or null disparity, respectively. This was even the case in neurons classified as monocular by conventional ocular dominance measurements. Spatial clustering of similarly tuned neurons was observed at a scale of about 10 μm. Finally, we probed neurons’ sensitivity to true stereo correspondence by comparing responses to correlated and anticorrelated RDS. Area LM, akin to primate ventral visual stream areas, showed higher selectivity for correlated stimuli and reduced anticorrelated responses, indicating higher-level disparity processing in LM compared to V1 and RL.


2012 ◽  
Vol 107 (9) ◽  
pp. 2335-2341 ◽  
Author(s):  
Kiley J. Seymour ◽  
Colin W. G. Clifford

Motion and binocular disparity are two features in our environment that share a common correspondence problem. Decades of psychophysical research dedicated to understanding stereopsis suggest that these features interact early in human visual processing to disambiguate depth. Single-unit recordings in the monkey also provide evidence for the joint encoding of motion and disparity across much of the dorsal visual stream. Here, we used functional MRI and multivariate pattern analysis to examine where in the human brain conjunctions of motion and disparity are encoded. Subjects sequentially viewed two stimuli that could be distinguished only by their conjunctions of motion and disparity. Specifically, each stimulus contained the same feature information (leftward and rightward motion and crossed and uncrossed disparity) but differed exclusively in the way these features were paired. Our results revealed that a linear classifier could accurately decode which stimulus a subject was viewing based on voxel activation patterns throughout the dorsal visual areas and as early as V2. This decoding success was conditional on some voxels being individually sensitive to the unique conjunctions comprising each stimulus, thus a classifier could not rely on independent information about motion and binocular disparity to distinguish these conjunctions. This study expands on evidence that disparity and motion interact at many levels of human visual processing, particularly within the dorsal stream. It also lends support to the idea that stereopsis is subserved by early mechanisms also tuned to direction of motion.


1962 ◽  
Vol 14 ◽  
pp. 149-155 ◽  
Author(s):  
E. L. Ruskol

The difference between average densities of the Moon and Earth was interpreted in the preceding report by Professor H. Urey as indicating a difference in their chemical composition. Therefore, Urey assumes the Moon's formation to have taken place far away from the Earth, under conditions differing substantially from the conditions of Earth's formation. In such a case, the Earth should have captured the Moon. As is admitted by Professor Urey himself, such a capture is a very improbable event. In addition, an assumption that the “lunar” dimensions were representative of protoplanetary bodies in the entire solar system encounters great difficulties.


1997 ◽  
Vol 161 ◽  
pp. 491-504 ◽  
Author(s):  
Frances Westall

AbstractThe oldest cell-like structures on Earth are preserved in silicified lagoonal, shallow sea or hydrothermal sediments, such as some Archean formations in Western Australia and South Africa. Previous studies concentrated on the search for organic fossils in Archean rocks. Observations of silicified bacteria (as silica minerals) are scarce for both the Precambrian and the Phanerozoic, but reports of mineral bacteria finds, in general, are increasing. The problems associated with the identification of authentic fossil bacteria and, if possible, closer identification of bacteria type can, in part, be overcome by experimental fossilisation studies. These have shown that not all bacteria fossilise in the same way and, indeed, some seem to be very resistent to fossilisation. This paper deals with a transmission electron microscope investigation of the silicification of four species of bacteria commonly found in the environment. The Gram positiveBacillus laterosporusand its spore produced a robust, durable crust upon silicification, whereas the Gram negativePseudomonas fluorescens, Ps. vesicularis, andPs. acidovoranspresented delicately preserved walls. The greater amount of peptidoglycan, containing abundant metal cation binding sites, in the cell wall of the Gram positive bacterium, probably accounts for the difference in the mode of fossilisation. The Gram positive bacteria are, therefore, probably most likely to be preserved in the terrestrial and extraterrestrial rock record.


1994 ◽  
Vol 144 ◽  
pp. 421-426
Author(s):  
N. F. Tyagun

AbstractThe interrelationship of half-widths and intensities for the red, green and yellow lines is considered. This is a direct relationship for the green and yellow line and an inverse one for the red line. The difference in the relationships of half-widths and intensities for different lines appears to be due to substantially dissimilar structuring and to a set of line-of-sight motions in ”hot“ and ”cold“ corona regions.When diagnosing the coronal plasma, one cannot neglect the filling factor - each line has such a factor of its own.


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