The overall aim is to understand how mechanisms in the lateral geniculate nucleus (LGN) and visual cortex analyze information about the chromatic properties of objects, and how these mechanisms determine human perceptual capabilities. Three closely connected groups of physiological studies are proposed. The first group will establish, through experiment and modeling, the underlying organization of chromatic selectivity in the receptive fields of neurons in LGN and cortex. The studies will answer the following questions: to what extent do the chromatic properties of a receptive field result from selection of inputs from cones of particular classes vs. selection of inputs from cones in particular positions; how does the silent region surrounding the receptive field shape a neuron's chromatic selectivity; do variations in contrast alter the chromatic selectivity of neurons? The second group of studies will characterize in cortical neurons the relationship between the chromatic properties and the binocular properties of receptive fields. One study will reveal whether and how neurons reconcile the conflicting demands that their two receptive fields have matched spatial properties and also matched chromatic properties; another will reveal how binocularly driven neurons combine different color signals arising in the two eyes. These studies are central to understanding binocular color mixture. The third group of studies will characterize mechanisms of chromatic adaptation that profoundly influence color sensitivity and appearance. One study will analyze the early signal transformations, expressed in LGN neurons, that are brought about by adaptation to mean chromaticity; another will analyze the subsequent transformations that occur in cortex--both those brought about by adaptation to the mean chromaticity, and those brought about by adaptation to chromatic contrast.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY004440-24
Application #
6912718
Study Section
Visual Sciences B Study Section (VISB)
Program Officer
Oberdorfer, Michael
Project Start
1982-07-01
Project End
2007-06-30
Budget Start
2005-07-01
Budget End
2006-06-30
Support Year
24
Fiscal Year
2005
Total Cost
$377,507
Indirect Cost
Name
New York University
Department
Neurology
Type
Schools of Arts and Sciences
DUNS #
041968306
City
New York
State
NY
Country
United States
Zip Code
10012
Goris, Robbe L T; Ziemba, Corey M; Movshon, J Anthony et al. (2018) Slow gain fluctuations limit benefits of temporal integration in visual cortex. J Vis 18:8
Goris, Robbe L T; Ziemba, Corey M; Stine, Gabriel M et al. (2017) Dissociation of Choice Formation and Choice-Correlated Activity in Macaque Visual Cortex. J Neurosci 37:5195-5203
Wang, Helena X; Movshon, J Anthony (2016) Properties of pattern and component direction-selective cells in area MT of the macaque. J Neurophysiol 115:2705-20
Kumbhani, Romesh D; El-Shamayleh, Yasmine; Movshon, J Anthony (2015) Temporal and spatial limits of pattern motion sensitivity in macaque MT neurons. J Neurophysiol 113:1977-88
Goris, Robbe L T; Simoncelli, Eero P; Movshon, J Anthony (2015) Origin and Function of Tuning Diversity in Macaque Visual Cortex. Neuron 88:819-31
Vintch, Brett; Movshon, J Anthony; Simoncelli, Eero P (2015) A Convolutional Subunit Model for Neuronal Responses in Macaque V1. J Neurosci 35:14829-41
Hallum, Luke E; Movshon, J Anthony (2014) Surround suppression supports second-order feature encoding by macaque V1 and V2 neurons. Vision Res 104:24-35
Goris, Robbe L T; Movshon, J Anthony; Simoncelli, Eero P (2014) Partitioning neuronal variability. Nat Neurosci 17:858-65
Freeman, Jeremy; Ziemba, Corey M; Heeger, David J et al. (2013) A functional and perceptual signature of the second visual area in primates. Nat Neurosci 16:974-81
Movshon, J Anthony (2013) Three comments on Teller's ""bridge locus"". Vis Neurosci 30:219-22

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