It is our general goal to relate perception of color and brightness to underlying physiological mechanisms. This program specifically investigates the physiological mechanisms of the primate visual cortex and how groups of neurons work together to process color-contrast and luminance-contrast information. Two experimental methods are employed: (1) microelectrode recording to determine the luminance sensitivities of cortical neurons and (2) the metabolic marker 14C-2-Deoxyglucose (2-DG) for identifying the grouping and patterning of color-sensitive and luminance-sensitive cortical neurons. Building upon the results of our initial experiments using electrophysiological techniques as well as the 14C-2-DG method, we propose to: (1) Describe, by microelectrode recordings, the luminance null point for a large population of cortical neurons stimulated by drifing heterochromatic two-color grating patterns; (2) By scanning microdensitometry, describe the column density profile across the layers of visual cortex induced by color-contrast and luminance-contrast stimulation; (3) By scanning microdensitometry, examine in detail the pattern periodicity following color or luminance visual stimulation; (4) By microdensitometry, examine the cortical mosaics produced by color or luminance stimulation to determine the degree of interleaving of the neuronal aggregation; (5) Compare and contrast (2)-(4) for striate and pre-striate locations; and (6) By computer-assisted stacking of sequential autoradiography re-construct the three dimensional distribution of these stimulus dependent patterns. The general proposition tested by these experiments is that the primate visual cortex is composed of stimulus specific functional elements or columns forming a three dimensional mosaic throughout. These columns are sensitive to luminance-contrast, color-contrast, orientation, motion, etc. and have distinctively different stimulus dependent trans-laminar 2-DG uptake forms.

Agency
National Institute of Health (NIH)
Institute
National Institute of Neurological Disorders and Stroke (NINDS)
Type
Research Project (R01)
Project #
5R01NS019342-06
Application #
3399394
Study Section
Biopsychology Study Section (BPO)
Project Start
1984-04-01
Project End
1993-06-30
Budget Start
1990-07-01
Budget End
1991-06-30
Support Year
6
Fiscal Year
1990
Total Cost
Indirect Cost
Name
University of Texas Health Science Center Houston
Department
Type
Schools of Medicine
DUNS #
City
Houston
State
TX
Country
United States
Zip Code
77225
Crawford, M L; Harwerth, R S; Chino, Y M et al. (1996) Binocularity in prism-reared monkeys. Eye (Lond) 10 ( Pt 2):161-6