scholarly journals Differential magnocellular versus parvocellular pathway contributions to the combinatorial processing of facial threat

Author(s):  
Reginald B. Adams ◽  
Hee Yeon Im ◽  
Cody Cushing ◽  
Jasmine Boshyan ◽  
Noreen Ward ◽  
...  
2019 ◽  
Vol 14 (2) ◽  
pp. 151-162 ◽  
Author(s):  
Cody A Cushing ◽  
Hee Yeon Im ◽  
Reginald B Adams Jr ◽  
Noreen Ward ◽  
Kestutis Kveraga

Author(s):  
Barnaby J. W. Dixson ◽  
Claire L. Barkhuizen ◽  
Belinda M. Craig
Keyword(s):  

1993 ◽  
Vol 04 (01) ◽  
pp. 43-54 ◽  
Author(s):  
CHRISTOPHER HIAN-ANN TING

In the mammalian visual system, magnocellular pathway and parvocellular pathway cooperatively process visual information in parallel. The magnocellular pathway is more global and less particular about the details while the parvocellular pathway recognizes objects based on the local features. In many aspects, Neocognitron may be regarded as the artificial analogue of the parvocellular pathway. It is interesting then to model the magnocellular pathway. In order to achieve "rotation invariance" for Neocognitron, we propose a neural network model after the magnocellular pathway and expand its roles to include surmising the orientation of the input pattern prior to recognition. With the incorporation of the magnocellular pathway, a basic shift in the original paradigm has taken place. A pattern is now said to be recognized when and only when one of the winners of the magnocellular pathway is validified by the parvocellular pathway. We have implemented the magnocellular pathway coupled with Neocognitron parallel on transputers; our simulation programme is now able to recognize numerals in arbitrary orientation.


Author(s):  
Mark Edwards ◽  
Stephanie C. Goodhew ◽  
David R. Badcock

AbstractThe visual system uses parallel pathways to process information. However, an ongoing debate centers on the extent to which the pathways from the retina, via the Lateral Geniculate nucleus to the visual cortex, process distinct aspects of the visual scene and, if they do, can stimuli in the laboratory be used to selectively drive them. These questions are important for a number of reasons, including that some pathologies are thought to be associated with impaired functioning of one of these pathways and certain cognitive functions have been preferentially linked to specific pathways. Here we examine the two main pathways that have been the focus of this debate: the magnocellular and parvocellular pathways. Specifically, we review the results of electrophysiological and lesion studies that have investigated their properties and conclude that while there is substantial overlap in the type of information that they process, it is possible to identify aspects of visual information that are predominantly processed by either the magnocellular or parvocellular pathway. We then discuss the types of visual stimuli that can be used to preferentially drive these pathways.


1996 ◽  
Vol 8 (7) ◽  
pp. 1427-1448 ◽  
Author(s):  
Harry G. Barrow ◽  
Alistair J. Bray ◽  
Julian M. L. Budd

This paper explores the possibility that the formation of color blobs in primate striate cortex can be partly explained through the process of activity-based self-organization. We present a simulation of a highly simplified model of visual processing along the parvocellular pathway, that combines precortical color processing, excitatory and inhibitory cortical interactions, and Hebbian learning. The model self-organizes in response to natural color images and develops islands of unoriented, color-selective cells within a sea of contrast-sensitive, orientation-selective cells. By way of understanding this topography, a principal component analysis of the color inputs presented to the network reveals that the optimal linear coding of these inputs keeps color information and contrast information separate.


2016 ◽  
Vol 33 ◽  
Author(s):  
FILIPP SCHMIDT ◽  
ANDREAS WEBER ◽  
ANKE HABERKAMP

AbstractVisual perception is not instantaneous; the perceptual representation of our environment builds up over time. This can strongly affect our responses to visual stimuli. Here, we study the temporal dynamics of visual processing by analyzing the time course of priming effects induced by the well-known Ebbinghaus illusion. In slower responses, Ebbinghaus primes produce effects in accordance with their perceptual appearance. However, in fast responses, these effects are reversed. We argue that this dissociation originates from the difference between early feedforward-mediated gist of the scene processing and later feedback-mediated more elaborate processing. Indeed, our findings are well explained by the differences between low-frequency representations mediated by the fast magnocellular pathway and high-frequency representations mediated by the slower parvocellular pathway. Our results demonstrate the potentially dramatic effect of response speed on the perception of visual illusions specifically and on our actions in response to objects in our visual environment generally.


Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 9-9 ◽  
Author(s):  
W H A Beaudot

An achromatic neuromorphic model of the vertebrate retina has already accounted for X and Y pathways (Beaudot and Hérault, 1994 Perception23 Supplement, 25) and has shown a temporal ‘coarse-to-fine’ processing of spatial information (Beaudot et al, 1995 Perception24 Supplement, 93). This model has been extended to colour vision. By taking into account the chromatic sensitivities of cones, functional properties of the parvocellular pathway are modelled. Approximating the responses of colour-opponent cells, the model provides a spatial multiplexing of luminance and chrominance information: sustained responses show spatial band-pass behaviour to luminance variations and low-pass behaviour to equiluminant colour changes. In addition the spatiotemporal inseparability for luminance in the parvocellular model leads to a temporal multiplexing of spatial luminance information: at higher temporal frequencies the spatial filtering is low-pass, conveying only luminance information. Demultiplexing this mixed information suggests interactions between retinal channels. By locally combining additive and subtractive mechanisms between opposite parvocellular pathways (eg G+/ R−± R+/ G−), and an inhibition from the magnocellular pathway, the existence of at least three functional subchannels is predicted: (i) a transient, spatially low-pass channel, (ii) a sustained, spatially band-pass channel, dedicated to the analysis of luminance information in a spatiotemporally separable way (eg moving shadows and static textures), and (iii) a spatiotemporally low-pass, colour-opponent channel leading to colour induction, which is little affected by the presence of shadows and is more representative of objects. This hypothesis of spatiotemporal demultiplexing of luminance and chrominance information, which should presumably occur at an early cortical level, is in accordance with the multiple-processing-streams organisation of the primate visual system.


2005 ◽  
Vol 494 (2) ◽  
pp. 260-274 ◽  
Author(s):  
Patricia R. Jusuf ◽  
Paul R. Martin ◽  
Ulrike Grünert

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