scholarly journals Biological Motion: Perceptual Processing, Neural Mechanisms and Clinical Application

2012 ◽  
Vol 24 (4) ◽  
pp. 357-392
Author(s):  
김제중
Perception ◽  
10.1068/p6320 ◽  
2009 ◽  
Vol 38 (4) ◽  
pp. 613-616 ◽  
Author(s):  
Russell Reid ◽  
Anna Brooks ◽  
Duncan Blair ◽  
Rick van der Zwan

Johansson (1973 Perception & Psychophysics14 201–211) suggested that point-light displays that are static—so-called ‘snapshots’—contain little or no information about the actor or their action. Here we present data that suggest even naive observers can perceive such information from static point-light arrays. Observers were able, at rates better than chance, to discriminate the directions of facing of sagittally viewed static point-light walkers. The data show also that, without feedback, performances improved with experience. Our data have implications for assumptions made in designing experiments with point-light displays and for models of the neural mechanisms mediating biological motion perceptions.


1999 ◽  
Vol 22 (6) ◽  
pp. 956-957
Author(s):  
Glyn W. Humphreys ◽  
M. Jane Riddoch

We discuss the difficulty of measuring the perceptual experience of colour, supporting Palmer's assertion that neuropsychological disorders of colour processing can be informative in this respect. We point out that some disorders seem to affect the perceptual experience of colour over and above the perceptual processing of colour, providing direct insights into the neural mechanisms supporting perceptual experience.


2003 ◽  
Vol 15 (8) ◽  
pp. 1095-1110 ◽  
Author(s):  
Yuhong Jiang ◽  
Nancy Kanwisher

Behavioral evidence supports a dissociation between response selection (RS; stimulus-to-response [S—R] mapping) and perceptual discrimination (PD): The former may be subject to a central processing bottleneck, whereas the latter is not (Pashler, 1994). We previously (Jiang & Kanwisher, 2003) identified a set of frontal and parietal regions involved in RS as those that produce a stronger signal when subjects follow a difficult S—R mapping rule than an easy mapping rule. Here, we test whether any of these regions are selectively activated by RS and not perceptual processing, as predicted by the central bottleneck view. In Experiment 1, subjects indicated which of four parallel lines was unique in length; PD was indexed by a higher BOLD response when the discrimination was difficult versus easy. Stimuli and responses were closely matched across conditions. We found that all regions-of-interest (ROIs) engaged by RS were also engaged by perceptual processing, arguing against the existence of mechanisms exclusively involved in RS. In Experiments 2 and 3, we asked what processes might go on in these ROIs, such that they could be recruited by both RS and perceptual processing. Our data argue against an account of this common activation in terms of spatial processing or general task difficulty. Thus, PD may recruit the same central processes that are engaged by RS.


2021 ◽  
Author(s):  
Arni Kristjansson

Attentional priming involves speeded selection of task-relevant visual search items when search stimuli remain constant from one search to the next. There is a tendency in the literature to interpret diverse priming effects as reflecting activity modulations of the same mechanisms. Priming effects in various different paradigms (from lower-level to higher-level features) have been used interchangeably to study the nature of priming, even when tasks differ vastly in difficulty and neural mechanisms involved. Another view is that priming is a characteristic of all perceptual mechanisms, that operate at different processing levels. Here, this issue was addressed by contrasting time courses and relative sizes of priming effects for repetition of a lower-level and higher-level feature (color vs. facial expression). Attentional priming was tested in two odd-one-out search tasks, one involving discrimination, the other present/absent judgment. Firstly, the sizes of the normalized priming effects were very different for color and expression and secondly, color priming effects lasted for much longer than expression priming, as measured with memory kernel analyses, suggesting that the mechanics behind the effects differ. These two forms of priming should therefore only be compared with great caution. Generally, the results suggest that priming occurs at many levels of processing and can take many forms. This view is highly consistent with research on the neural mechanisms of priming. Priming of attention shifts should be thought of as a general principle of perceptual processing.


eLife ◽  
2018 ◽  
Vol 7 ◽  
Author(s):  
Nadine Dijkstra ◽  
Pim Mostert ◽  
Floris P de Lange ◽  
Sander Bosch ◽  
Marcel AJ van Gerven

Visual perception and imagery rely on similar representations in the visual cortex. During perception, visual activity is characterized by distinct processing stages, but the temporal dynamics underlying imagery remain unclear. Here, we investigated the dynamics of visual imagery in human participants using magnetoencephalography. Firstly, we show that, compared to perception, imagery decoding becomes significant later and representations at the start of imagery already overlap with later time points. This suggests that during imagery, the entire visual representation is activated at once or that there are large differences in the timing of imagery between trials. Secondly, we found consistent overlap between imagery and perceptual processing around 160 ms and from 300 ms after stimulus onset. This indicates that the N170 gets reactivated during imagery and that imagery does not rely on early perceptual representations. Together, these results provide important insights for our understanding of the neural mechanisms of visual imagery.


2017 ◽  
Author(s):  
Nadine Dijkstra ◽  
Pim Mostert ◽  
Floris P. de Lange ◽  
Sander Bosch ◽  
Marcel A. J. van Gerven

Visual perception and imagery rely on similar representations in the visual cortex. During perception, visual activity is characterized by distinct processing stages, but the temporal dynamics underlying imagery remain unclear. Here, we investigated the dynamics of visual imagery in human participants using magnetoencephalography. We show that, contrary to perception, the onset of imagery is characterized by broad temporal generalization. Furthermore, there is consistent overlap between imagery and perceptual processing around 150 ms and from 300 ms after stimulus onset, presumably reflecting completion of the feedforward sweep and perceptual stabilization respectively. These results indicate that during imagery either the complete representation is activated at once and does not include low-level visual areas, or the order in which visual features are activated is less fixed and more flexible than during perception. These findings have important implications for our understanding of the neural mechanisms of visual imagery.


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