| ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Cerebral Cortex 1994; 4:555-572
© Oxford University Press 1994
research-article |
Functional Segregation of Color and Motion Processing in the Human Visual Cortex: Clinical Evidence
Intelligent Systems Laboratory, Departments of Biomedical Engineering and Neurology, Boston University, Boston, Massachusetts 02215, Center for Biological and Computational Learning, Massachusetts Institute of Technology, Boston, Massachusetts, and Departments of Neurology and Surgery, Brigham and Women's Hospital, Harvard Medical School, Boston, Massachusetts 02115
Anatomical and physiological investigations indicate two major distinct functional streams within the extrastriate visual cortex of the macaque monkey, and behavioral observations suggest that the ventral (occipitotemporal) pathway is the cornerstone for object recognition whereas the dorsal (occipitoparietal) pathway is primarily involved in visuospatial perception and visuomotor performance. In the context of this dichotomy we conducted a psychophysical and neuropsychological study of visual perceptual abilities in two stroke patients, each with lesions involving several extrastriate areas. Magnetic resonance imaging demonstrated bilateral lesions; in one patient (E.W.) the lesion involves the ventral medial portions of the occipital and temporal lobes, and in the other (A.F.) the lesion involves dorsally the occipital-parietal area, including the region of the temporal-parietal-occipital junction. E.W. suffers from achromatopsia of central origin, prosopagnosia, visual agnosia, and alexia without agraphia. His depth and motion perception, including recognition of moving objects, are normal. He has superior visual field loss bilaterally, and slightly impaired acuity, and complains that the world appears in a deep twilight even on a sunny day. In contrast, A.F. shows specific deficits of stereopsis, spatial localization, and several aspects of motion perception. He is also impaired at recognizing objects presented from unconventional views, but recognition of prototypical views of objects, and color and form discrimination are normal, as is his ability to recognize faces.
The anatomical characteristics of the lesions of these two patients permit a direct experimental comparison of the effects of lesions confined to the parietal or temporal pathways. E.W.'s and A.F.'s performance on the psychophysical and neuropsychological tasks discussed here supports the functional distinction between a dorsal and a ventral extrastriate system but additionally suggests the existence of a pathway involved in identification-from-motion that is separate from both the dorsal early motion/spatial analysis pathway and the ventral color/static-form pathway.
![]()
CiteULike
Connotea
Del.icio.us What's this?
This article has been cited by other articles:
![]() |
B. R. Conway and D. Y. Tsao Color Architecture in Alert Macaque Cortex Revealed by fMRI Cereb Cortex, November 1, 2006; 16(11): 1604 - 1613. [Abstract] [Full Text] [PDF] |
||||
![]() |
M. Kusunoki, K. Moutoussis, and S. Zeki Effect of Background Colors on the Tuning of Color-Selective Cells in Monkey Area V4 J Neurophysiol, May 1, 2006; 95(5): 3047 - 3059. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Vaina and C. G. Gross Perceptual deficits in patients with impaired recognition of biological motion after temporal lobe lesions PNAS, November 30, 2004; 101(48): 16947 - 16951. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Moutoussis and S. Zeki Responses of Spectrally Selective Cells in Macaque Area V2 to Wavelengths and Colors J Neurophysiol, April 1, 2002; 87(4): 2104 - 2112. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Vaina, J. Solomon, S. Chowdhury, P. Sinha, and J. W. Belliveau Functional neuroanatomy of biological motion perception in humans PNAS, September 5, 2001; (2001) 191374198. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Moutoussis and S. Zeki A psychophysical dissection of the brain sites involved in color-generating comparisons PNAS, June 14, 2000; (2000) 110570897. [Abstract] [Full Text] |
||||
![]() |
S. Zeki, S. Aglioti, D. McKeefry, and G. Berlucchi The neurological basis of conscious color perception in a blind patient PNAS, November 23, 1999; 96(24): 14124 - 14129. [Abstract] [Full Text] [PDF] |
||||
![]() |
P. Giannakopoulos, G. Gold, M. Duc, J.-P. Michel, P. R. Hof, and C. Bouras Neuroanatomic correlates of visual agnosia in Alzheimer's disease: A clinicopathologic study Neurology, January 1, 1999; 52(1): 71 - 71. [Abstract] [Full Text] [PDF] |
||||
![]() |
S. Zeki {blacksquare} REVIEW : Parallel Processing, Asynchronous Perception, and a Distributed System of Consciousness in Vision Neuroscientist, September 1, 1998; 4(5): 365 - 372. [Abstract] [PDF] |
||||
![]() |
A. Puce, T. Allison, S. Bentin, J. C. Gore, and G. McCarthy Temporal Cortex Activation in Humans Viewing Eye and Mouth Movements J. Neurosci., March 15, 1998; 18(6): 2188 - 2199. [Abstract] [Full Text] [PDF] |
||||
![]() |
K. Moutoussis and S. Zeki A psychophysical dissection of the brain sites involved in color-generating comparisons PNAS, July 5, 2000; 97(14): 8069 - 8074. [Abstract] [Full Text] [PDF] |
||||
![]() |
L. M. Vaina, J. Solomon, S. Chowdhury, P. Sinha, and J. W. Belliveau Functional neuroanatomy of biological motion perception in humans PNAS, September 25, 2001; 98(20): 11656 - 11661. [Abstract] [Full Text] [PDF] |
||||





