Back
Acta Physiologica 2011; Volume 203, Supplement 688
The 62nd National Congress of the Italian Physiological Society
9/25/2011-9/27/2011
Sorrento, Italy
CODING OF LUMINANCE CONTRAST BY MACAQUE V4 NEURONS: STIMULUS ENERGY OR BASIC FEATURE?
Abstract number: O56
SANI1,2 I, SANTANDREA1,2 E, GOLZAR3 A, FORGHIERI1,2 M, CHELAZZI1,2 L
1Dept of Neurological, Neuropsychological, Morphological and Movement Sciences, Univ. of Verona Medical School, Verona, Italy
2Italian Institute of Neuroscience, Verona, Italy
3Dept of Physiology, McGill Univ., Montral, Qubec
Contrast is a key ingredient of the visual world and it is indispensable for image perception. A particular form of it is luminance contrast, the physical quantity that specifies the relative variation in luminance of a visual stimulus compared to the background.
Most cortical visual neurons display a sigmoidal increase of their firing with respect to stimulus contrast, which has thus been conceived as a modulation of stimulus energy. However, psychophysical evidence shows that human observers are able to attentively select items of non-maximal contrasts, suggesting that at least a fraction of cortical visual neurons might show a non-monotonic tuning profile in response to varying contrast levels.
To explore this possibility, we recorded responses of individual neurons in macaque area V4d to a set of stimuli spanning the complete range of stimulus contrasts, and we finely explored their contrast response function (CRF) - a critical step in order to achieve a full understanding of the way in which luminance contrast is encoded by the given neuron.
Besides neurons with traditional CRFs, we found neurons which were not appreciably modulated by contrast - a candidate correlate for the phenomenon of contrast invariance in object recognition - and, most crucially, neurons showing a non-monotonic tuning profile in response to varying stimulus contrast for which contrast is to be considered as a feature of the stimulus instead of a factor determining stimulus strength.
To cite this abstract, please use the following information:
Acta Physiologica 2011; Volume 203, Supplement 688 :O56