kanizsa figure
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2019 ◽  
Vol 72 (7) ◽  
pp. 1741-1755 ◽  
Author(s):  
Siyi Chen ◽  
Qi-Yang Nie ◽  
Hermann J Müller ◽  
Markus Conci

Previous work has demonstrated that perceptual grouping modulates the selectivity of attention across space. By contrast, how grouping influences the allocation of attention over time is much less clear. This study investigated this issue, using an attentional blink (AB) paradigm to test how grouping influences the initial selection and the subsequent short-term memory consolidation of a target. On a given trial, two red Kanizsa-type targets (T1 and T2) with varying grouping strength were embedded in a rapid serial visual presentation stream of irrelevant distractors. Our results showed the typical AB finding: impaired identification of T2 when presented close in time following T1. Moreover, the AB was modulated by the T2 grouping—independently of the T1 structure—with stronger grouping leading to a decreased AB and overall higher performance. Conversely, a reversed pattern, namely an increased AB with increasing grouping strength was observed when the Kanizsa figure was not task-relevant. Together, these findings suggest that the grouping benefit emerges at early perceptual stages, automatically drawing attentional resources, thereby leading to either sustained benefits or transient costs—depending on the task-relevance of the grouped object. This indicates that grouping modulates processing of objects in time.


Perception ◽  
2018 ◽  
Vol 47 (12) ◽  
pp. 1153-1165 ◽  
Author(s):  
Michael Kavšek ◽  
Stephanie Braun

The addition of crossed horizontal disparity enhances the clarity of illusory contours compared to pictorial illusory contours and illusory contours with uncrossed horizontal disparity. Two infant-controlled habituation–dishabituation experiments explored the presence of this effect in infants 5 months of age. Experiment 1 examined whether infants are able to distinguish between a Kanizsa figure with crossed horizontal disparity and a Kanizsa figure with uncrossed horizontal disparity. Experiment 2 tested infants for their ability to differentiate between a Kanizsa figure with crossed horizontal disparity and a two-dimensional Kanizsa figure. The results provided evidence that the participants perceived the two- and the three-dimensional illusory Kanizsa contour, the illusory effect in which was strengthened by the addition of crossed horizontal disparity.


2018 ◽  
Vol 44 (9) ◽  
pp. 1399-1413 ◽  
Author(s):  
Siyi Chen ◽  
Stefan Glasauer ◽  
Hermann J. Müller ◽  
Markus Conci

2018 ◽  
Vol 18 (10) ◽  
pp. 1114
Author(s):  
Markus Conci ◽  
Qi-Yang Nie ◽  
Hermann Müller ◽  
Siyi Chen

2014 ◽  
Vol 26 (5) ◽  
pp. 955-969 ◽  
Author(s):  
Annelinde R. E. Vandenbroucke ◽  
Johannes J. Fahrenfort ◽  
Ilja G. Sligte ◽  
Victor A. F. Lamme

Every day, we experience a rich and complex visual world. Our brain constantly translates meaningless fragmented input into coherent objects and scenes. However, our attentional capabilities are limited, and we can only report the few items that we happen to attend to. So what happens to items that are not cognitively accessed? Do these remain fragmentary and meaningless? Or are they processed up to a level where perceptual inferences take place about image composition? To investigate this, we recorded brain activity using fMRI while participants viewed images containing a Kanizsa figure, an illusion in which an object is perceived by means of perceptual inference. Participants were presented with the Kanizsa figure and three matched nonillusory control figures while they were engaged in an attentionally demanding distractor task. After the task, one group of participants was unable to identify the Kanizsa figure in a forced-choice decision task; hence, they were “inattentionally blind.” A second group had no trouble identifying the Kanizsa figure. Interestingly, the neural signature that was unique to the processing of the Kanizsa figure was present in both groups. Moreover, within-subject multivoxel pattern analysis showed that the neural signature of unreported Kanizsa figures could be used to classify reported Kanizsa figures and that this cross-report classification worked better for the Kanizsa condition than for the control conditions. Together, these results suggest that stimuli that are not cognitively accessed are processed up to levels of perceptual interpretation.


2011 ◽  
Vol 49 (9) ◽  
pp. 2456-2464 ◽  
Author(s):  
Markus Conci ◽  
Thomas Töllner ◽  
Marcin Leszczynski ◽  
Hermann J. Müller

Perception ◽  
10.1068/p6272 ◽  
2009 ◽  
Vol 38 (9) ◽  
pp. 1313-1327 ◽  
Author(s):  
Hermann Bulf ◽  
Eloisa Valenza ◽  
Francesca Simion

The aim of the present study was to investigate how perceptual binding and selective attention operate during infants' and adults' visual search of an illusory figure. An eye-tracker system was used to test adults and infants in two conditions: illusory and non-illusory (real). In the illusory condition, a Kanizsa triangle was embedded among distractor pacmen which did not generate illusory contours. In the non-illusory condition, a real triangle was included in the same pacmen's display. The results showed that adults detected both the Kanizsa and the real figure automatically and without focal attention (experiment 1). In contrast, 6-month-old infants showed a pop-out effect only for the real figure (experiment 2). The failure of the illusory figure to trigger infants' attention was not due to infants' inability to perceive the illusory figure per se, as infants preferred the illusory figure over a non-illusory control stimulus in a classical preferential-looking task (experiment 3). Overall, these findings indicate that the illusory Kanizsa triangle triggers visual attention in adults, but not in infants, supporting evidence that at 6 months of age the binding processes involved in the perception of a Kanizsa figure do not operate in an adult-like manner.


2007 ◽  
Vol 69 (8) ◽  
pp. 1278-1294 ◽  
Author(s):  
Markus Conci ◽  
Hermann J. Müller ◽  
Mark A. Elliott

2007 ◽  
Vol 19 (1) ◽  
pp. 91-101 ◽  
Author(s):  
Marianne Maertens ◽  
Stefan Pollmann

Our visual percepts are not fully determined by the physical stimulus input. That is why we perceive crisp bounding contours even in the absence of luminance-defined borders in visual illusions such as the Kanizsa figure. It is important to understand which neural processes are involved in creating these artificial visual experiences because this might tell us how we perceive coherent objects in natural scenes, which are characterized by mutual overlap. We have already shown using functional magnetic resonance imaging [Maertens, M., & Pollmann, S. fMRI reveals a common neural substrate of illusory and real contours in v1 after perceptual learning. Journal of Cognitive Neuroscience, 17, 1553–1564, 2005] that neurons in the primary visual cortex (V1) respond to these stimuli. Here we provide support for the hypothesis that V1 is obligatory for the discrimination of the curvature of illusory contours. We presented illusory contours across the portion of the visual field corresponding to the physiological “blind spot.” Four observers were extensively trained and asked to discriminate fine curvature differences in these illusory contours. A distinct performance drop (increased errors and response latencies) was observed when illusory contours traversed the blind spot compared to when they were presented in the “normal” contralateral visual field at the same eccentricity. We attribute this specific performance deficit to the failure to build up a representation of the illusory contour in the absence of a cortical representation of the “blind spot” within V1. The current results substantiate the assumption that neural activity in area V1 is closely related to our phenomenal experience of illusory contours in particular, and to the construction of our subjective percepts in general.


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