Conflict-induced perceptual filtering: A mechanism supporting location-specific control?

2020 ◽  
pp. 174702182097701
Author(s):  
Blaire J Weidler ◽  
Emily R Cohen-Shikora ◽  
Julie M Bugg

Cognitive control can adapt to the level of conflict present in the environment in a proactive (pre-stimulus onset) or reactive (post-stimulus onset) manner. This is evidenced by list-wide and location-specific proportion congruence effects, reduced interference in higher conflict lists or locations, respectively. Proactive control in the flanker task is believed to be supported by a conflict-induced-filtering (CIF) mechanism. The goal of the present set of experiments was to test if CIF also supports reactive location-specific control in the flanker task. To measure CIF, we interspersed a visual search task with a flanker task. After reproducing evidence for CIF using a two-location, list-wide proportion congruence manipulation (Experiment 1), we examined if a similar pattern emerges using a location-specific proportion congruence manipulation in Experiments 2 - 5. We found minimal evidence that reactive location-specific control employs a CIF mechanism. What was clear, however, is that the location-specific proportion congruence effect is susceptible to disruption from an intermixed task that dilutes the location-conflict signal. This highlights the need for alternative approaches to elucidate whether CIF or another mechanism supports reactive, location-specific control.

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 147-147
Author(s):  
P Stivalet ◽  
Y Moreno ◽  
C Cian ◽  
J Richard ◽  
P-A Barraud

In a visual search paradigm we measured the stimulus onset asynchrony (SOA) between a stimulus and a mask that was required to reach 90% correct responses. This procedure has the advantage of taking into account the real processing time and excluding the time for the generation of the motor response. Twelve congenitally deaf adult subjects and twelve normal subjects were given a visual search task for a target letter O among a varying number of distractor letters Q and vice-versa. In both groups we found the asymmetrical visual search pattern classically observed with parallel processing for the search for the target Q and with serial processing for the search for the target O (Treisman, 1985 Computer Vision, Graphics, and Image Processing31 156 – 177). The difference between the mean search slopes for an O target was not statistically significant between the groups; this might be due to the variability within the groups. The visual search amidst the congenitally deaf does not seem to benefit from a compensatory effect in relation to the acoustic deprivation. Our results seem to confirm data reported by Neville (1990 Annals of the New York Academy of Science 71 – 91) obtained by an electrophysiological technique based on event-related potentials. Nevertheless, the deaf subjects were 2.5 times faster at the visual search task.


2006 ◽  
Vol 44 (8) ◽  
pp. 1137-1145 ◽  
Author(s):  
Oren Kaplan ◽  
Reuven Dar ◽  
Lirona Rosenthal ◽  
Haggai Hermesh ◽  
Mendel Fux ◽  
...  

2003 ◽  
Vol 41 (10) ◽  
pp. 1365-1386 ◽  
Author(s):  
Steven S. Shimozaki ◽  
Mary M. Hayhoe ◽  
Gregory J. Zelinsky ◽  
Amy Weinstein ◽  
William H. Merigan ◽  
...  

2006 ◽  
Vol 18 (8) ◽  
pp. 1331-1342 ◽  
Author(s):  
Andrea Kübler ◽  
Veronica Dixon ◽  
Hugh Garavan

The ability to exert control over automatic behavior is of particular importance as it allows us to interrupt our behavior when the automatic response is no longer adequate or even dangerous. However, despite the literature that exists on the effects of practice on brain activation, little is known about the neuroanatomy involved in reestablishing executive control over previously automatized behavior. We present a visual search task that enabled participants to automatize according to defined criteria within about 3 hr of practice and then required them to reassert control without changing the stimulus set. We found widespread cortical activation early in practice. Activation in all frontal areas and in the inferior parietal lobule decreased significantly with practice. Only selected prefrontal (Brodmann's areas [BAs] 9/46/8) and parietal areas (BAs 39/40) were specifically reactivated when executive control was required, underlining the crucial role of the dorsolateral prefrontal cortex in executive control to guide our behavior.


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