It is possible to discriminate between grating contrasts over a 300-fold contrast range, whereas V1 neurons have very limited dynamic ranges. Using populations of model neurons with contrast-response parameters taken from electrophysiological studies (cat and macaque), we investigated ways of combining responses to code contrast over the full range. One model implemented a pooling rule that retained information about individual response patterns. The second summed responses indiscriminately. We measured accuracy of contrast identification over a wide range of contrasts and found the first model to be more accurate; the mutual information between actual and estimated contrast was also greatest for this model. The accuracy peak for the population of cat neurons coincided with the peak of the distribution of contrasts in natural images, suggesting an ecological match. Macaque neurons seem better able to code contrasts that are slightly higher on average than those found in the natural environment.
The dipper effect for contrast discrimination provides strong evidence that the underlying neural response is accelerating at low contrasts and saturating at high contrasts. The contrast-response functions of V1 neurons do have this sigmoidal shape, but individual neurons do not generally have a dynamic range wide enough to account for the dipper effect. This paper presents a Bayesian model of neurons in monkey V1, whose contrast-response function is described by a modified Naka-Rushton with multiplicative noise. It is shown that a model of groups of twelve or more neurons gives a reasonable explanation of the psychophysical data of two observers, but there is a large systematic error which is apparently due to the shape of the distribution of the monkey's sensitivity parameter, c50. A further model provides a better fit to the data by sacrificing strict adherence to V1 neuronal parameters and, instead using an arbitrary bimodal c50 distribution, perhaps reflecting differences between M- and P-cells.
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