competing stimuli
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Author(s):  
Scott A. Middlebrooks ◽  
Xueying Zhao ◽  
Roseanne M. Ford ◽  
Peter T. Cummings




2021 ◽  
Author(s):  
Jonathan D. Schmidt ◽  
John M. Falligant ◽  
Amanda Goetzel ◽  
Shelby Hardisty ◽  
Louis P. Hagopian


2020 ◽  
Vol 20 (7) ◽  
pp. 27
Author(s):  
Alex Hernández-García ◽  
Ricardo Ramos Gameiro ◽  
Alessandro Grillini ◽  
Peter König


i-Perception ◽  
2020 ◽  
Vol 11 (3) ◽  
pp. 204166952092904
Author(s):  
Stuart Anstis ◽  
Grace Hong ◽  
Alan Ho

A test cross that flickers between light yellow and dark blue at 5 to 8Hz looks apparently yellow on a dark gray surround and apparently blue on a light gray surround ( flicker augmented contrast). The achromatic surround cannot be inducing the perceived colors. Instead, the visual system selects the more salient apparent color with the higher Michelson contrast. The same is true for dichoptic vision. When one eye views a steady, light yellow cross and the other eye views a congruent steady dark blue cross, the binocular combination of colors looks apparently yellow on a dark gray surround and apparently blue on a light gray surround. Thus, when competing stimuli are distributed over time (flicker) or space (dichoptic vision), the visual system overweights the stimulus with the higher contrast. To see objects clearly, we accept the best view of any object and downplay inferior alternatives.



Author(s):  
John Michael Falligant ◽  
Ashley Carver ◽  
Jennifer Zarcone ◽  
Jonathan D. Schmidt


2019 ◽  
Author(s):  
Alex Hernández-García ◽  
Ricardo Ramos Gameiro ◽  
Alessandro Grillini ◽  
Peter König

Current computational models of visual salience accurately predict the distribution of fixations on isolated visual stimuli. It is not known, however, whether the global salience of a stimulus, that is its effectiveness in the competition for attention with other stimuli, is a function of the local salience or an independent measure. Further, do task and familiarity with the competing images influence eye movements? Here, we investigated the direction of the first saccade to characterize and analyze the global visual salience of competing stimuli. Participants freely observed pairs of images while eye movements were recorded. The pairs balanced the combinations of new and already seen images, as well as task and task-free trials. Then, we trained a logistic regression model that accurately predicted the location---left or right image---of the first fixation for each stimulus pair, accounting too for the influence of task, familiarity and lateral bias. The coefficients of the model provided a reliable measure of global salience, which we contrasted with two distinct local salience models, GBVS and Deep Gaze. The lack of correlation of the behavioral data with the former and the small correlation with the latter indicate that global salience cannot be explained by the feature-driven local salience of images. Further, the influence of task and familiarity was rather small and we reproduced the previously reported left-sided bias. Summarized, we showed that natural stimuli have an intrinsic global salience related to the human initial gaze direction, independent of the local salience and little influenced by task and familiarity.



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