2,155 research outputs found

    Change blindness: eradication of gestalt strategies

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    Arrays of eight, texture-defined rectangles were used as stimuli in a one-shot change blindness (CB) task where there was a 50% chance that one rectangle would change orientation between two successive presentations separated by an interval. CB was eliminated by cueing the target rectangle in the first stimulus, reduced by cueing in the interval and unaffected by cueing in the second presentation. This supports the idea that a representation was formed that persisted through the interval before being 'overwritten' by the second presentation (Landman et al, 2003 Vision Research 43149–164]. Another possibility is that participants used some kind of grouping or Gestalt strategy. To test this we changed the spatial position of the rectangles in the second presentation by shifting them along imaginary spokes (by ±1 degree) emanating from the central fixation point. There was no significant difference seen in performance between this and the standard task [F(1,4)=2.565, p=0.185]. This may suggest two things: (i) Gestalt grouping is not used as a strategy in these tasks, and (ii) it gives further weight to the argument that objects may be stored and retrieved from a pre-attentional store during this task

    Is the rapid adaptation paradigm too rapid? Implications for face and object processing

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    The final publication is available at Elsevier via http://dx.doi.org/10.1016/j.neuroimage.2012.03.065. © 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/Rapid adaptation is an adaptation procedure in which adaptors and test stimuli are presented in rapid succession. The current study tested the validity of this method for early ERP components by investigating the specificity of the adaptation effect on the face-sensitive N170 ERP component across multiple test stimuli. Experiments 1 and 2 showed identical response patterns for house and upright face test stimuli using the same adaptor stimuli. The results were also identical to those reported in a previous study using inverted face test stimuli (Nemrodov and Itier, 2011). In Experiment 3 all possible adaptor-test combinations between upright face, house, chair and car stimuli were used and no interaction between adaptor and test category, expected in the case of test-specific adaptation, was found. These results demonstrate that the rapid adaptation paradigm does not produce category-specific adaptation effects around 170-200 ms following test stimulus onset, a necessary condition for the interpretation of adaptation results. These results suggest the rapid categorical adaptation paradigm does not work.103305-1/Canadian Institutes of Health Research89822-1/Canadian Institutes of Health ResearchMOP-89822/Canadian Institutes of Health Researc

    Is the rapid adaptation paradigm too rapid? Implications for face and object processing

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    The final publication is available at Elsevier via http://dx.doi.org/10.1016/j.neuroimage.2012.03.065. © 2012. This manuscript version is made available under the CC-BY-NC-ND 4.0 license http://creativecommons.org/licenses/by-nc-nd/4.0/Rapid adaptation is an adaptation procedure in which adaptors and test stimuli are presented in rapid succession. The current study tested the validity of this method for early ERP components by investigating the specificity of the adaptation effect on the face-sensitive N170 ERP component across multiple test stimuli. Experiments 1 and 2 showed identical response patterns for house and upright face test stimuli using the same adaptor stimuli. The results were also identical to those reported in a previous study using inverted face test stimuli (Nemrodov and Itier, 2011). In Experiment 3 all possible adaptor-test combinations between upright face, house, chair and car stimuli were used and no interaction between adaptor and test category, expected in the case of test-specific adaptation, was found. These results demonstrate that the rapid adaptation paradigm does not produce category-specific adaptation effects around 170-200 ms following test stimulus onset, a necessary condition for the interpretation of adaptation results. These results suggest the rapid categorical adaptation paradigm does not work.103305-1/Canadian Institutes of Health Research89822-1/Canadian Institutes of Health ResearchMOP-89822/Canadian Institutes of Health Researc

    Neural responses to dynamic adaptation reveal the dissociation between the processing of the shape of contours and textures

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    This research was supported by a Leverhulme Trust grant (RPG-2016-056) awarded to Elena Gheorghiu (PI) and Jasna Martinovic (co-PI). The C code used to generate the contours, written in conjunction with routines from the VISAGE graphics library (Cambridge Research System) was modified from code originally written by Frederick A. A. Kingdom. We would like to thank Frederick Kingdom for helping with the development of the original C code.Peer reviewedPostprin

    Aerospace medicine and biology: A continuing bibliography with indexes (supplement 333)

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    This bibliography lists 122 reports, articles and other documents introduced into the NASA Scientific and Technical Information System during January, 1990. Subject coverage includes: aerospace medicine and psychology, life support systems and controlled environments, safety equipment, exobiology and extraterrestrial life, and flight crew behavior and performance

    Temporal and spatial localization of prediction-error signals in the visual brain

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    It has been suggested that the brain pre-empts changes in the environment through generating predictions, although real-time electrophysiological evidence of prediction violations in the domain of visual perception remain elusive. In a series of experiments we showed participants sequences of images that followed a predictable implied sequence or whose final image violated the implied sequence. Through careful design we were able to use the same final image transitions across predictable and unpredictable conditions, ensuring that any differences in neural responses were due only to preceding context and not to the images themselves. EEG and MEG recordings showed that early (N170) and mid-latency (N300) visual evoked potentials were robustly modulated by images that violated the implied sequence across a range of types of image change (expression deformations, rigid-rotations and visual field location). This modulation occurred irrespective of stimulus object category. Although the stimuli were static images, MEG source reconstruction of the early latency signal (N/M170) localized expectancy violation signals to brain areas associated with motion perception. Our findings suggest that the N/M170 can index mismatches between predicted and actual visual inputs in a system that predicts trajectories based on ongoing context. More generally we suggest that the N/M170 may reflect a “family” of brain signals generated across widespread regions of the visual brain indexing the resolution of top-down influences and incoming sensory data. This has important implications for understanding the N/M170 and investigating how the brain represents context to generate perceptual predictions

    Prior experience modulates top-down predictive processing in the ventral visual areas

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    Repetition suppression(RS)refers to that the reduction of neural activities for repeated presentations of a given stimulus compared to its first presentation. Summerfield et al(2008) found the magnitude of RS is affected by the repetition probability of stimuli, called as P(rep) effect. Based on the predictive coding theory, prior experience about the sensory inputs is necessary to optimally achieve cognitive processes. But it remains unclear how prior experience modulates predictive processes. To address this issue, in Study I, we estimated the P(rep) effects for Chinese characters and German words in native Chinese and German participants to test whether prior experience affects the P(rep) effect of lexical stimuli. The results showed that the P(rep) effect is only manifest for words of a language with which participants had prior experience. Study II performed fMRI measurements before and after a 10-day perceptual learning (PL) training for cars to test the modulation of short-term experience on the P(rep) effect. The results replicated the P(rep) effect for faces and cars. More interestingly, the P(rep) effect can be temporarily abolished by the short-term PL experience. The third study investigated how prior experience modulates sensory inputs. Study 3a adopted a classic stimulus repetition paradigm to measure RS for faces, together with either concurrent short-term memory (STM) load or a control condition. The results showed that RS is significantly attenuated when visual STM is loaded. Study 3b manipulates attention by a face inversion detection task. The results showed that the RS effect appears in the STM condition when participants attend to faces. The main conclusions: i) predictive processes, as measured by the P(rep) effect, require extensive prior experiences with stimuli, but ii) these can also be modulated by short-term learning experience. Further, iii) STM and attention are two modulators of prior experiences on predictive processes
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