Abstract
Primate vision relies on retinotopically organized cortical parcels defined by representations of hemifield (upper versus lower visual field), eccentricity (fovea versus periphery), and area (V1, V2, V3, V4). Here we test for functional signatures of these organizing principles. We used fMRI to measure responses to gratings varying in spatial frequency, color, and saturation across retinotopically defined parcels in two macaque monkeys, and we developed a Sparse Supervised Embedding (SSE) analysis to identify stimulus features that best distinguish cortical parcels from each other. Constraining the SSE model to distinguish just eccentricity representations of the voxels revealed the expected variation of spatial frequency and S-cone modulation with eccentricity. Constraining the model according to the dorsal-ventral location and retinotopic area of each voxel provided unexpected functional signatures, which we investigated further with standard univariate analyses. Posterior parcels (V1) were distinguished from anterior parcels (V4) by differential responses to chromatic and luminance contrast, especially of low spatial frequency gratings. Meanwhile, ventral parcels were distinguished from dorsal parcels by differential responses to chromatic and luminance contrast, especially of colors that modulate all three cone types. The dorsal-ventral asymmetry not only resembled differences between candidate dorsal and ventral subdivisions of human V4, but also extended to include all retinotopic visual areas, starting in V1 and increasing from V1 to V4. The results provide insight into the functional roles of different retinotopic areas and demonstrate the utility of Sparse Supervised Embedding as a data-driven tool for generating hypotheses about cortical function and behavior.
Significance Statement This study demonstrates a new analysis, Sparse Supervised Embedding (SSE), which promises to be useful for visualizing and understanding complex neuroimaging datasets. The paper uses SSE to explore the functional roles of retinotopic visual areas (V1, V2, V3, V4, V3a, MT). The results show that retinotopic areas parcellated by representations for eccentricity and upper/lower visual hemifield have functional signatures, which are defined by unique combinations of responses to color, spatial frequency, and contrast. The functional signatures provide hypotheses for the different roles that the parcels play in vision and help resolve apparent differences between human and macaque visual cortex organization.
Footnotes
We thank Rosa Lafer-Sousa for help collecting the fMRI data and Eli Merriam, Chris Baker, Christian Quaia, and two anonymous reviewers for constructive feedback on earlier drafts of this work. We thank L. Wald and A. Mareyam for providing the four-channel magnetic resonance coil. This research was supported by the National Eye Institute Intramural Research Program, as well as grants from the National Science Foundation (0918064 to BRC), the US National Institutes of Health (EY023322 to BRC), the Whitehall Foundation (BRC), and Wellesley College (BRC). The imaging was carried out at the Athinoula A. Martinos Center for Biomedical Imaging at the Massachusetts General Hospital, using resources provided by the Center for Functional Neuroimaging Technologies (P41EB015896) and a P41 Biotechnology Resource grant supported by the National Institute of Biomedical Imaging and Bioengineering. This work also involved the use of instrumentation supported by the US National Institutes of Health Shared Instrumentation Grant Program and/or High-End Instrumentation Grant Program (S10RR021110).
This is an open-access article distributed under the terms of the Creative Commons Attribution 4.0 International license, which permits unrestricted use, distribution and reproduction in any medium provided that the original work is properly attributed.