Hostname: page-component-76fb5796d-5g6vh Total loading time: 0 Render date: 2024-04-28T08:38:58.970Z Has data issue: false hasContentIssue false

Effect of sawtooth polarity on chromatic and luminance detection

Published online by Cambridge University Press:  02 June 2009

Paul J. DeMarco Jr
Affiliation:
Visual Sciences Center, The University of Chicago, 939 East 57th St., Chicago
Vivianne C. Smith
Affiliation:
Visual Sciences Center, The University of Chicago, 939 East 57th St., Chicago
Joel Pokorny
Affiliation:
Visual Sciences Center, The University of Chicago, 939 East 57th St., Chicago

Abstract

Psychophysical studies have documented that many observers show lower thresholds for rapid-off than for rapid-on sawtooth luminance modulation. This finding, together with physiological findings from chromatically opponent ganglion cells of the macaque monkey, prompted a search for a similar bias in psychophysical detection of chromatic increments and decrements of light. Using a luminance pedestal in conjunction with a luminance background to favor detection by chromatic mechanisms, we measured spectral sensitivity for rapid-on and rapid-off sawtooth stimuli presented spatially coextensive with the pedestal. There were two different pedestal chromaticities: one broadband, and the second composed only of long-wavelength light to enhance short-wavelength-sensitive, cone-mediated detection. Spectral-sensitivity measurements for different wavelength stimuli revealed no systematic differences across the visible spectrum as a function of sawtooth waveform polarity or pedestal chromaticity. Similarly, temporal contrast-sensitivity functions for hetero-chromatically modulated red-green sawtooth stimuli did not reveal an asymmetry in sensitivity for rapid-red and rapid-green chromatic change. Some of the observers showed a higher sensitivity for luminance modulated rapid-off sawtooth stimuli, as also noted in previous studies. This asymmetry was not found when a white luminance pedestal and background was used. These results suggest that the cone inputs to chromatically opponent ON- and OFF-center cells are sufficiently balanced to provide equivalent psychophysical thresholds for chromatic increments and decrements of light.

Type
Research Articles
Copyright
Copyright © Cambridge University Press 1994

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

Bowen, R.W., Pokorny, J. & Smith, V.C (1989). Sawtooth contrast sensitivity: Decrements have the edge. Vision Research 29, 15011509.Google Scholar
Bowen, R.W., Pokorny, J., Smith, V.C. & Fowler, M.A. (1992). Sawtooth contrast sensitivity: Effects of mean illuminance and low temporal frequencies. Vision Research 32, 12391247.Google Scholar
Cole, G.R., Stromeyer, C.F. & Kronauer, R.E. (1990). Visual interactions with luminance and chromatic stimuli. Journal of the Optical Society of America A 7, 128140.CrossRefGoogle ScholarPubMed
de Monasterio, F.M. (1979). Asymmetry of on- and off-pathways of blue sensitive cones of the retina of macaques. Brain Research 166, 3948.CrossRefGoogle Scholar
Derrington, A.M., Krauskopf, J. & Lennie, P. (1984). Chromatic mechanisms in lateral geniculate nucleus of macaque. Journal of Physiology 357, 241265.Google Scholar
DeValois, R.L. (1965). Analysis of coding of color vision in the primate visual system. Cold Spring Harbor Symposium on Quantitative Biology 30, 567579.Google Scholar
Elsner, A.E., Pokorny, J. & Burns, S.A. (1986). Chromaticity discrimination: Effects of luminance contrast and spatial frequency. Journal of the Optical Society of America A 3, 916920.CrossRefGoogle ScholarPubMed
Famiglietti, E.V., Kaneko, A. & Tachibana, M. (1977). Neuronal architecture of on and off pathways to ganglion cells in carp retina. Science 198, 12671269.CrossRefGoogle Scholar
Foster, D.H. & Snelgar, R.S. (1983). Test and field spectral sensitivities of colour mechanisms obtained on small white backgrounds: Action of unitary opponent-colour processes? Vision Research 23, 787797.Google Scholar
Frumkes, T.E., Lange, G., Denny, N. & Beczkowska, I. (1992). Influence of rod adaptation upon cone responses to light offset in humans: I. Results in normal observers. Visual Neuroscience 8, 8389.Google Scholar
Gouras, P. (1968). Identification of cone mechanisms in monkey ganglion cells. Journal of Physiology (London) 199, 533547.Google Scholar
Hanley, M. & McKay, D.M. (1979). Polarity-sensitive perceptual adaptation to temporal sawtooth modulation of luminance. Experimental Brain Research 35, 3746.Google Scholar
Howell, D.C. (1987). Statistical Methods for Psychology (2nd ed.). Boston, Massachusetts: PWS Publishers.Google Scholar
Kaplan, E. & Shapley, R. (1986). The primate retina contains two types of ganglion cells with high and low contrast sensitivity. Proceedings of the National Academy of Sciences of the U.S.A. 83, 27552757.CrossRefGoogle ScholarPubMed
Kelly, D.H. (1971). Theory of flicker and transient responses. Journal of the Optical Society of America 61, 537546.Google Scholar
Kelly, D.H. (1975). Luminous and chromatic flickering fields have opposite effects. Science 188, 371372.Google Scholar
Kelly, D.H. & van Norren, D. (1977). Two-band model of hetero-chromatic flicker. Journal of the Optical Society of America 67, 10811091.CrossRefGoogle Scholar
Kouyama, N. & Marshak, D.W. (1992). Bipolar cells specific for blue cones in the macaque retina. Journal of Neuroscience 12, 12331252.CrossRefGoogle ScholarPubMed
Krauskopf, J. (1980). Discrimination and detection of changes in luminance. Vision Research 20, 671677.CrossRefGoogle ScholarPubMed
Krauskopf, J., Williams, D.R. & Heeley, D.W. (1982). Cardinal directions of color space. Vision Research 22, 11231131.Google Scholar
Kremers, J., Lee, B.B., Pokorny, J.P. & Smith, V.C. (1993). Responses of macaque ganglion cells to periodic waveforms in relation to psychophysical sensitivity. Vision Research 33, 19972011.Google Scholar
Lee, B.B., Pokorny, J., Smith, V.C, Martin, P.R. & Valberg, A. (1990). Luminance and chromatic modulation sensitivity of macaque ganglion cells and human observers. Journal of the Optical Society of American A 7, 22232236.Google Scholar
Malpeli, J.G. & Schiller, P.H. (1978). Lack of blue off-center cells in the visual system of the monkey. Brain Research 141, 385389.CrossRefGoogle ScholarPubMed
Marshak, D.W., Aldrich, L.B., Del, Valle J. & Yamada, T. (1990). Localization of immunoreactive cholecystokinin precursor to amacrine cells and bipolar cells of the macaque monkey retina. Journal of Neuroscience 10, 30453055.CrossRefGoogle ScholarPubMed
Nacer, A., Murray, I.J. & Carden, D. (1989). Interactions between luminance mechanisms and colour opponency. In Seeing Contour and Color, ed. Kulikowski, J.J., Dickinson, C.M, & Murray, I.J., pp. 357360. Oxford: Pergamon Press.Google Scholar
Nelson, R., Famiglietti, E.V. & Kolb, H. (1978). Intracellular staining reveals different levels of stratification for on- and off-center ganglion cells in cat retina. Journal of Neurophysiology 41, 472483.Google Scholar
Priest, I.G. & Brickwedde, F.G. (1938). Minimum perceptible colorimetric purity as a function of dominant wavelength. Journal of the Optical Society of America 33, 133139.Google Scholar
Purdy, D.M.L. (1931). Spectral hue as a function of intensity. American Journal of Psychology 43, 541559.CrossRefGoogle Scholar
Schiller, P.H. (1984). The connections of the retinal on and off pathways to the lateral geniculate nucleus of the monkey. Vision Research 24, 923932.Google Scholar
Schiller, P.H. (1992). The ON and OFF channels of the visual system. Trends in Neurosciences 15, 8692.Google Scholar
Schiller, P.H., Sandell, J.H. & Maunsell, J.H.R. (1986). Functions of the on and off channels of the visual system. Nature 322, 824825.Google Scholar
Shapley, R.M. & Reid, R.C (1992). Spatial structure of cone inputs to receptive fields in primate lateral geniculate nucleus. Nature 356, 716718.Google Scholar
Smith, E.L., Harwerth, R.S., Crawford, M.J.L. & Duncan, G.C (1989). Contribution of retinal ON channels to scotopic and photopic spectral sensitivity. Visual Neuroscience 3, 225239.Google Scholar
Smith, V.C, Lee, B.B., Pokorny, J., Martin, P.R. & Valberg, A. (1992). Responses of macaque ganglion cells to the relative phase of heterochromatically modulated lights. Journal of Physiology 458, 191221.Google Scholar
Smith, V.C, Pokorny, J. & Lee, B.B. (1991). The contrast gain of P- and M-pathway cells expressed in cone contrast units. Investigative Ophthalmology and Visual Science (Supp.) 32, 1034.Google Scholar
Snelgar, R.S., Foster, D.H. & Scase, M.O. (1987). Isolation of opponent-colour mechanisms at increment threshold. Vision Research 27, 10171027.Google Scholar
Sperling, H.G. & Harwerth, R.S. (1971). Red-green cone interaction in the increment-threshold spectral sensitivity of primates. Science 172, 180184.Google Scholar
Swanson, W.H., Ueno, T., Smith, V.C. & Pokorny, J. (1987). Temporal modulation sensitivity and pulse detection thresholds for chromatic and luminance perturbations. Journal of the Optical Society of America A 4, 19922005.Google Scholar
Switkes, E., Bradley, A. & De Valois, K.K. (1988). Contrast dependence and mechanisms of masking interactions among chromatic and luminance gratings. Journal of the Optical Society of America A 5, 11491162.CrossRefGoogle ScholarPubMed
Ueno, T., Pokorny, J. & Smith, V.C. (1985). Reaction times to chromatic stimuli. Vision Research 25, 16231627.CrossRefGoogle ScholarPubMed
Ueno, T. & Swanson, W.H. (1989). Response pooling between chromatic and luminance systems. Vision Research 29, 325333.Google Scholar
Valberg, A., Lee, B.B. & Tigwell, D.A. (1986). Neurones with strong inhibitory S-cone inputs in the macaque lateral geniculate nucleus. Vision Research 26, 10611064.CrossRefGoogle ScholarPubMed
Valberg, A., Lee, B.B. & Tryti, J. (1987). Simulation of responses of spectrally-opponent neurones in the macaque lateral geniculate nucleus to chromatic and achromatic light stimuli. Vision Research 27, 867882.Google Scholar
Wiesel, T. & Hubel, D.H. (1966). Spatial and chromatic interactions in the lateral geniculate body of the rhesus monkey. Journal of Neurophysiology 29, 11151156.Google Scholar
Wright, W.D. & Pitt, F.H.G. (1937). The saturation-discrimination of two trichromats. Proceedings of the Physical Society (London) 49, 329331.CrossRefGoogle Scholar
Yeh, T., Pokorny, J. & Smith, V.C. (1993). Chromatic discrimination with variation in chromaticity and luminance: Data and theory. Vision Research 33, 18351845.Google Scholar
Zrenner, E. & Gouras, P. (1981). Characteristics of the blue sensitive cone mechanism on primate retinal ganglion cells. Vision Research 21, 16051609.Google Scholar