Contrast adaptation may enhance contrast discrimination

2002 ◽  
Vol 16 (1) ◽  
pp. 45-58 ◽  
Author(s):  
Giulia Abbonizio ◽  
Colin Clifford ◽  
Keith Langley
2010 ◽  
Vol 51 (2) ◽  
pp. 920 ◽  
Author(s):  
Allison M. McKendrick ◽  
Geoff P. Sampson ◽  
Mark J. Walland ◽  
David R. Badcock

2021 ◽  
Author(s):  
Noga Pinchuk Yacobi ◽  
Dov Sagi

The effects of contrast adaptation and contrast area summation were investigated using a contrast discrimination task. The task consisted of a target of variable size, and a pedestal with a fixed base contrast. Discrimination performance was examined for a condition in which the pedestal size was fixed, equal to the largest target size, and for a condition in which the pedestal size matched the target size and thus varied with it. Repeated performance of the task produced rapid within-session improvements for both conditions. For stimuli with a matching size of target and pedestal, the performance improved only for the larger targets, indicating the development of area summation, which was initially absent for these stimuli. However, the improvements were mostly temporary, and were not fully retained between subsequent sessions. The temporary nature of the sensitivity gains implies that they resulted, at least in part, from rapid adaptation to the stimulus contrast. We suggest that adaptation decorrelates and thus reduces the spatial noise generated by a high-contrast pedestal, leading to improved area summation and better contrast sensitivity. A decorrelation model successfully predicted our experimental results.


2014 ◽  
Vol 112 (11) ◽  
pp. 2834-2849 ◽  
Author(s):  
Yuko Hara ◽  
Justin L. Gardner

Prior information about the relevance of spatial locations can vary in specificity; a single location, a subset of locations, or all locations may be of potential importance. Using a contrast-discrimination task with four possible targets, we asked whether performance benefits are graded with the spatial specificity of a prior cue and whether we could quantitatively account for behavioral performance with cortical activity changes measured by blood oxygenation level-dependent (BOLD) imaging. Thus we changed the prior probability that each location contained the target from 100 to 50 to 25% by cueing in advance 1, 2, or 4 of the possible locations. We found that behavioral performance (discrimination thresholds) improved in a graded fashion with spatial specificity. However, concurrently measured cortical responses from retinotopically defined visual areas were not strictly graded; response magnitude decreased when all 4 locations were cued (25% prior probability) relative to the 100 and 50% prior probability conditions, but no significant difference in response magnitude was found between the 100 and 50% prior probability conditions for either cued or uncued locations. Also, although cueing locations increased responses relative to noncueing, this cue sensitivity was not graded with prior probability. Furthermore, contrast sensitivity of cortical responses, which could improve contrast discrimination performance, was not graded. Instead, an efficient-selection model showed that even if sensory responses do not strictly scale with prior probability, selection of sensory responses by weighting larger responses more can result in graded behavioral performance benefits with increasing spatial specificity of prior information.


1991 ◽  
Vol 87 (1) ◽  
Author(s):  
L.M. M��tt�nen ◽  
J.J. Koenderink

Perception ◽  
1972 ◽  
Vol 1 (3) ◽  
pp. 341-349 ◽  
Author(s):  
I Bodis-Wollner ◽  
C D Hendley ◽  
J J Kulikowski

Contrast-modulated grating patterns were used to compare evoked responses and psychophysical thresholds of contrast modulation. The stimulus consisted of the successive presentation of a grating pattern at a higher and lower contrast. At a modulation rate of 8 Hz it was found that there is correspondence between the two kinds of data for a 6 cycle/degree grating. The just noticeable difference was not constant, and data approximated a Weber's law of contrast discrimination. However, it was found that there is a slight departure from this law, in that the ratio decreases with mean contrast. Both psychophysical and electrophysiological data exclude a model of simple luminance detection and are consistent with the operation of spatial contrast detectors in the human visual system.


2007 ◽  
Vol 98 (3) ◽  
pp. 1287-1296 ◽  
Author(s):  
Kate S. Gaudry ◽  
Pamela Reinagel

Sensory neurons appear to adapt their gain to match the variance of signals along the dimension they encode, a property we shall call “contrast normalization.” Contrast normalization has been the subject of extensive physiological and theoretical study. We previously found that neurons in the lateral geniculate nucleus (LGN) exhibit contrast normalization in their responses to full-field flickering white-noise stimuli, and that neurons with the strongest contrast normalization best preserved information transmission across a range of contrasts. We have also shown that both of these properties could be reproduced by nonadapting model cells. Here we present a detailed comparison of this nonadapting model to physiological data from the LGN. First, the model cells recapitulated other contrast dependencies of LGN responses: decreasing stimulus contrast resulted in an increase in spike-timing jitter and spike-number variability. Second, we find that the extent of contrast normalization in this model depends on model parameters related to refractoriness and to noise. Third, we show that the model cells exhibit rapid, transient changes in firing rate just after changes in contrast, and that this is sufficient to produce the transient changes in information transmission that have been reported in other neurons. It is known that intrinsic properties of neurons change during contrast adaptation. Nevertheless the model demonstrates that the spiking nonlinearity of neurons can produce many of the temporal aspects of contrast gain control, including normalization to input variance and transient effects of contrast change.


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