JN Ad Instruments
HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
 QUICK SEARCH:   [advanced]


     


J Neurophysiol 95: 2638-2649, 2006. First published December 28, 2005; doi:10.1152/jn.01016.2005
0022-3077/06 $8.00
This Article
Right arrow Full Text
Right arrow Full Text (PDF)
Right arrow All Versions of this Article:
95/4/2638    most recent
01016.2005v1
Right arrow Alert me when this article is cited
Right arrow Alert me if a correction is posted
Right arrow Citation Map
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Download to citation manager
Citing Articles
Right arrow Citing Articles via HighWire
Right arrow Citing Articles via Web of Science (3)
Right arrow Citing Articles via Google Scholar
Google Scholar
Right arrow Articles by Vladusich, T.
Right arrow Articles by Cornelissen, F. W.
Right arrow Search for Related Content
PubMed
Right arrow PubMed Citation
Right arrow Articles by Vladusich, T.
Right arrow Articles by Cornelissen, F. W.

Do Cortical Neurons Process Luminance or Contrast to Encode Surface Properties?

Tony Vladusich1, Marcel P. Lucassen2 and Frans W. Cornelissen1

1Laboratory of Experimental Ophthalmology and NeuroImaging Centre, School of Behavioural and Cognitive Neurosciences, University Medical Centre Groningen, University of Groningen, Groningen 2Department of Human Interfaces, Netherlands Organization for Applied Scientific Research-Human Factors, Soesterberg, The Netherlands

Submitted 27 September 2005; accepted in final form 25 December 2005

On the one hand, contrast signals provide information about surface properties, such as reflectance, and patchy illumination conditions, such as shadows. On the other hand, processing of luminance signals may provide information about global light levels, such as the difference between sunny and cloudy days. We devised models of contrast and luminance processing, using principles of logarithmic signal coding and half-wave rectification. We fit each model to individual response profiles obtained from 67 surface-responsive macaque V1 neurons in a center-surround paradigm similar to those used in human psychophysical studies. The most general forms of the luminance and contrast models explained, on average, 73 and 87% of the response variance over the sample population, respectively. We used a statistical technique, known as Akaike's information criterion, to quantify goodness of fit relative to number of model parameters, giving the relative probability of each model being correct. Luminance models, having fewer parameters than contrast models, performed substantially better in the vast majority of neurons, whereas contrast models performed similarly well in only a small minority of neurons. These results suggest that the processing of local and mean scene luminance predominates over contrast integration in surface-responsive neurons of the primary visual cortex. The sluggish dynamics of luminance-related cortical activity may provide a neural basis for the recent psychophysical demonstration that luminance information dominates brightness perception at low temporal frequencies.


Address for reprint requests and other correspondence: T. Vladusich, Laboratory of Experimental Ophthalmology and NeuroImaging Centre, School of Behavioural and Cognitive Neurosciences, University Medical Centre Groningen, University of Groningen, PO Box 30.001, Groningen 9700 RB, The Netherlands (E-mail: t.vladusich{at}med.umcg.nl)




This article has been cited by other articles:


Home page
J. Neurophysiol.Home page
X. Huang and M. A. Paradiso
V1 Response Timing and Surface Filling-In
J Neurophysiol, July 1, 2008; 100(1): 539 - 547.
[Abstract] [Full Text] [PDF]




HOME HELP FEEDBACK SUBSCRIPTIONS ARCHIVE SEARCH TABLE OF CONTENTS
Visit Other APS Journals Online
Copyright © 2006 by the The American Physiological Society.