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Organization of the Human Trichromatic Cone Mosaic
Abstract
Using high-resolution adaptive-optics imaging combined with retinal densitometry, we characterized the arrangement of short- (S), middle- (M), and long- (L) wavelength-sensitive cones in eight human foveal mosaics. As suggested by previous studies, we found males with normal color vision that varied in the ratio of L to M cones (from 1.1:1 to 16.5:1). We also found a protan carrier with an even more extreme L:M ratio (0.37:1). All subjects had nearly identical S-cone densities, indicating independence of the developmental mechanism that governs the relative numerosity of L/M and S cones. L:M cone ratio estimates were correlated highly with those obtained in the same eyes using the flicker photometric electroretinogram (ERG), although the comparison indicates that the signal from each M cone makes a larger contribution to the ERG than each L cone. Although all subjects had highly disordered arrangements of L and M cones, three subjects showed evidence for departures from a strictly random rule for assigning the L and M cone photopigments. In two retinas, these departures corresponded to local clumping of cones of like type. In a third retina, the L:M cone ratio differed significantly at two retinal locations on opposite sides of the fovea. These results suggest that the assignment of L and M pigment, although highly irregular, is not a completely random process. Surprisingly, in the protan carrier, in which X-chromosome inactivation would favor L- or M-cone clumping, there was no evidence of clumping, perhaps as a result of cone migration during foveal development.
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“At 1 degree eccentric from the fovea, the average percentage of cones that were identified as S cones by adaptive optics was 5.72 percent, and the S cones are distributed in a relatively regular hexagonal array (Hofer et al., 2005).”
From The genetics of normal and defective color vision (2011) · cites this paper as Hofer et al., 2005
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“This explains the slight clumpiness that has been observed for the human L/M cone mosaic (Hofer, Carroll, Neitz, Neitz & Williams, 2005).”
From The genetics of normal and defective color vision (2011) · cites this paper as Hofer et al., 2005
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Gene Action in the X-chromosome of the Mouse (Mus musculus L.)
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Sorted by citations
The genetics of normal and defective color vision
Neitz, J., & Neitz, M. (2011) · Vision Research · doi:10.1016/j.visres.2010.12.002 · Cited by 377
Self-citationMelanopsin- and L-cone–induced pupil constriction is inhibited by S- and M-cones in humans
Woelders, T., Leenheers, T., Gordijn, M. C. M., Hut, R. A., Beersma, D. G. M., & Wams, E. J. (2018) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1716281115 · Cited by 81
Metadata
- Authors
- Hofer, H., Carroll, J., Neitz, J., Neitz, M., & Williams, D. R.
- Venue
- The Journal of Neuroscience
- Publisher
- Society for Neuroscience
- Published
- 2005-10-19
- Volume
- 25
- Issue
- 42
- Pages
- 9669-9679
- ISSN
- 0270-6474
- 1529-2401
- Cited by
- 364
- References
- 1
- Language
- en
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