The general goal of the research is to understand how signals that originate in rods and in each of the three types of cone combine in the various pathways that mediate human visual function. Most work in this area has addressed only the signals originating in foveal cones. A more general model requires that we understand how signals from both rods and cones contribute to channels subserving the full range of visual functions. The proposed experiments investigate several aspects of extrafoveal pathways by means of psychophysical experiments using adult human observers. One set of experiments investigates the properties of putative dual scotopic (rod) pathways, with special attention to differences in their involvement with cone signals and in their importance for spatial, temporal and increment sensitivity. The experiments derive from a model that integrates physiological, anatomical, and psychophysical evidence for dual rod pathways. Whether the experiments support or refute the model, they will provide empirical evidence on the general importance of dual rod pathways. A second set of experiments characterizes the separate components of the adaptation processes by which rod signals regulate incremental sensitivity of cone pathways (cone-rod interaction), using probe-on-flash and other psychophysical techniques. The experiments will also separate adaptation mechanisms that operate in local retinal areas from those operating at greater distance by means of lateral pathways. A third set of experiments determines the involvement of rod signals in opponent pathways, including both spectrally- and chromatically-opponent pathways. The experiments aim to resolve presently conflicting evidence, reveal which types of opponent pathways are influenced by rod signals, and investigate the role of rod signals in human color vision. The general strategy of all experiments is to employ variation of psychophysical task and of spectral, spatial and temporal stimulus parameters of select different mechanisms or pathways for study. Psychophysical tasks include measurements of incremental, temporal (flicker), and spatial (grating) sensitivities. Signals from rods and from identifiable cone types can then be used as probes to describe detection and adaptation pathways and the quantitative rules for combination of rod and cone signals.

Agency
National Institute of Health (NIH)
Institute
National Eye Institute (NEI)
Type
Research Project (R01)
Project #
5R01EY003221-12
Application #
2158730
Study Section
Visual Sciences B Study Section (VISB)
Project Start
1987-03-01
Project End
1995-06-30
Budget Start
1993-05-01
Budget End
1995-06-30
Support Year
12
Fiscal Year
1993
Total Cost
Indirect Cost
Name
University of Washington
Department
Psychology
Type
Schools of Arts and Sciences
DUNS #
135646524
City
Seattle
State
WA
Country
United States
Zip Code
98195
Knight, Roger; Buck, Steven L (2002) Time-dependent changes of rod influence on hue perception. Vision Res 42:1651-62
Buck, S L; Knight, R F; Bechtold, J (2000) Opponent-color models and the influence of rod signals on the loci of unique hues. Vision Res 40:3333-44
Verweij, J; Dacey, D M; Peterson, B B et al. (1999) Sensitivity and dynamics of rod signals in H1 horizontal cells of the macaque monkey retina. Vision Res 39:3662-72
Knight, R; Buck, S L; Fowler, G A et al. (1998) Rods affect S-cone discrimination on the Farnsworth-Munsell 100-hue test. Vision Res 38:3477-81
Buck, S L; Knight, R; Fowler, G et al. (1998) Rod influence on hue-scaling functions. Vision Res 38:3259-63
Buck, S L (1997) Influence of rod signals on hue perception: evidence from successive scotopic contrast. Vision Res 37:1295-301
Buck, S L; Knight, R (1994) Partial additivity of rod signals with M- and L-cone signals in increment detection. Vision Res 34:2537-45
Knight, R; Buck, S L (1993) Cone pathways and the pi 0 and pi 0' rod mechanisms. Vision Res 33:2203-13
Buck, S L; Knight, R (1991) Test-additivity experiments: different procedures, different results. J Opt Soc Am A 8:696-8
Buck, S L; Pulos, E (1987) Rod-cone interaction in monocular but not binocular pathways. Vision Res 27:479-82

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