Abstract:We examined whether the processing of discontinuities involved in figure-ground segmentation, like line ends, can be modulated under selective attention conditions. Subjects decided whether a gap in collinear or parallel lines was located to the right or left. Two stimuli were displayed in immediate succession. When the gaps were on the same side, reaction times (RTs) for the second stimulus increased when collinear lines followed parallel lines, or the reverse, but only when the two stimuli shared the same or… Show more
“…# These are sometimes visible, like in the Ehrenstein illusion ( Figure 2, Gove et al, 1995 ;Lesher and Mingolla, 1993 ;von der Heydt and Peterhans, 1989 ;Westheimer and Li, 1996). In our stimuli, perpendicular lines are not consciously perceived, but are nevertheless produced (Giersch, 2001 ;Giersch and Fahle, 2002 ;Giersch and Caparos, 2005 ;Gurnsey et al, 1999 ;von der Heydt and Peterhans, 1989).…”
Section: Collinear Elementsmentioning
confidence: 51%
“…When the gap to be detected is between parallel elements, however, the two line terminations forming the gap produce a perpendicular line that is in exactly the same place as the gap and closes the stimulus (Figure 2b). We have suggested that the processing of line terminations is modulated in healthy volunteers (Giersch and Caparos, 2005 ;Giersch and Fahle, 2002), and that lorazepam affects this modulation (review in Giersch, 2001 ;Lorenceau et al, 2005), which explains why lorazepam-treated subjects separate elements even when they are collinear, at least when contour processing is modulated. Several studies have suggested that the effects of lorazepam on the processing of line terminations thus impairs the binding of the local elements composing the object (Giersch et al, 1997 ;Giersch and Lorenceau, 1999 ;Lorenceau et al, 2005).…”
Section: Collinear Elementsmentioning
confidence: 99%
“…For the sake of simplicity, we focus here on the conditions allowing a modulation of contour processing to be observed, i.e. when the two consecutive stimuli change in form (Giersch and Fahle, 2002 ;Giersch and Caparos, 2005). These are the conditions in which a deleterious effect of an acute dose of lorazepam has been observed (Giersch, 2001).…”
Acute effects of lorazepam on visual information processing, perceptual priming and explicit memory are well established. However, visual processing and perceptual priming have rarely been explored in long-term lorazepam users. By exploring these functions it was possible to test the hypothesis that difficulty in processing visual information may lead to deficiencies in perceptual priming. Using a simple blind procedure, we tested explicit memory, perceptual priming and visual perception in 15 long-term lorazepam users and 15 control subjects individually matched according to sex, age and education level. Explicit memory, perceptual priming, and the identification of fragmented pictures were found to be preserved in long-term lorazepam users, contrary to what is usually observed after an acute drug intake. The processing of visual contour, on the other hand, was still significantly impaired. These results suggest that the effects observed on low-level visual perception are independent of the acute deleterious effects of lorazepam on perceptual priming. A comparison of perceptual priming in subjects with low- vs. high-level identification of new fragmented pictures further suggests that the ability to identify fragmented pictures has no influence on priming. Despite the fact that they were treated with relatively low doses and far from peak plasma concentration, it is noteworthy that in long-term users memory was preserved.
“…# These are sometimes visible, like in the Ehrenstein illusion ( Figure 2, Gove et al, 1995 ;Lesher and Mingolla, 1993 ;von der Heydt and Peterhans, 1989 ;Westheimer and Li, 1996). In our stimuli, perpendicular lines are not consciously perceived, but are nevertheless produced (Giersch, 2001 ;Giersch and Fahle, 2002 ;Giersch and Caparos, 2005 ;Gurnsey et al, 1999 ;von der Heydt and Peterhans, 1989).…”
Section: Collinear Elementsmentioning
confidence: 51%
“…When the gap to be detected is between parallel elements, however, the two line terminations forming the gap produce a perpendicular line that is in exactly the same place as the gap and closes the stimulus (Figure 2b). We have suggested that the processing of line terminations is modulated in healthy volunteers (Giersch and Caparos, 2005 ;Giersch and Fahle, 2002), and that lorazepam affects this modulation (review in Giersch, 2001 ;Lorenceau et al, 2005), which explains why lorazepam-treated subjects separate elements even when they are collinear, at least when contour processing is modulated. Several studies have suggested that the effects of lorazepam on the processing of line terminations thus impairs the binding of the local elements composing the object (Giersch et al, 1997 ;Giersch and Lorenceau, 1999 ;Lorenceau et al, 2005).…”
Section: Collinear Elementsmentioning
confidence: 99%
“…For the sake of simplicity, we focus here on the conditions allowing a modulation of contour processing to be observed, i.e. when the two consecutive stimuli change in form (Giersch and Fahle, 2002 ;Giersch and Caparos, 2005). These are the conditions in which a deleterious effect of an acute dose of lorazepam has been observed (Giersch, 2001).…”
Acute effects of lorazepam on visual information processing, perceptual priming and explicit memory are well established. However, visual processing and perceptual priming have rarely been explored in long-term lorazepam users. By exploring these functions it was possible to test the hypothesis that difficulty in processing visual information may lead to deficiencies in perceptual priming. Using a simple blind procedure, we tested explicit memory, perceptual priming and visual perception in 15 long-term lorazepam users and 15 control subjects individually matched according to sex, age and education level. Explicit memory, perceptual priming, and the identification of fragmented pictures were found to be preserved in long-term lorazepam users, contrary to what is usually observed after an acute drug intake. The processing of visual contour, on the other hand, was still significantly impaired. These results suggest that the effects observed on low-level visual perception are independent of the acute deleterious effects of lorazepam on perceptual priming. A comparison of perceptual priming in subjects with low- vs. high-level identification of new fragmented pictures further suggests that the ability to identify fragmented pictures has no influence on priming. Despite the fact that they were treated with relatively low doses and far from peak plasma concentration, it is noteworthy that in long-term users memory was preserved.
“…The output of this integration process is then forwarded to higher-level regions responding to global pattern structure (e.g., the lateral occipital complex [LOC], more anterior temporal cortex). Consistent with this view, lesions to intermediate visual areas are associated with disorders in the organization of visual elements into recognizable whole patterns (Giersch, 2002;Milner et al, 1991;Riddoch & Humphreys, 1987).…”
Hierarchical models of visual processing assume that global pattern recognition is contingent on the progressive integration of local elements across larger spatial regions, operating from early through intermediate to higher-level cortical regions. Here, we present results from neuropsychological fMRI that refute such models. We report two patients, one with lesions to intermediate ventral regions and the other with damage around the intraparietal sulcus (IPS). The patient with ventral damage showed normal behavioral and BOLD responses to global Glass patterns. The patient with IPS damage was impaired in discriminating global patterns and showed a lack of significant responses to these patterns in intermediate visual regions spared by the lesion. However, this patient did show BOLD activity to translational patterns, where local element relations are important. These results suggest that activation of intermediate ventral regions is not necessary to code global patterns; instead global patterns are coded in a heterarchical fashion. High-level regions of dorsal cortex are necessary to generate global pattern coding in intermediate ventral regions; in contrast, local integration processes are not sufficient.
“…We argue that local–global processing, that is, the classical distinction between the coding of details and global forms (Navon, 1977), is not enough to resolve such cases, because neither pair of individuals corresponds to either local information (one individual) or global information (the crowd). It does not suppress the risk of fragmentation that may occur when two objects that belong to two different groups must be considered as one (Giersch & Caparos, 2005; Giersch & Fahle, 2002). This question is all the more crucial because it can in fact occur quite often in everyday life, for instance, in cases where visual scenes are rich and complex.…”
The study attempted to distinguish automatic grouping processes from top-down processes in a visual perceptual task in 30 patients with schizophrenia and 30 matched controls. Participants decided whether 7 figures were all different or whether 2 adjacent figures were identical. The distance between figures was manipulated to produce 3 separated pairs of figures, the targets belonging to either the same pair (within-group trials) or different pairs (between-groups trials). As controls, patients benefited from proximity for grouping. Top-down processes were explored by manipulating the proportion of within-group and between-groups trials in 3 experimental blocks. In patients, response times (RTs) decreased for within-group trials when within-group trials were more frequent, indicating that performance was correctly adapted to the type of block. Unlike controls, however, this RT decrease was not accompanied by a cost for between-groups trials. Ocular movement recordings revealed that controls were able to focus on between-groups regions selectively when between-groups trials were more frequent, whereas patients were unable to do so. The authors suggest that top-down processes allowing the construction of a selective representation of between-groups regions are impaired in patients with schizophrenia.
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