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C F Stromeyer

Publications and source records attributed to C F Stromeyer.

At least 37 records · Page 2Linked to original sources
PubMed1991

Temporal phase response of the short-wave cone signal for color and luminance.

A chromatic discrimination paradigm was used to measure the temporal phase of the S (short-wave cone) signal relative to the L--M (long-wave cone minus middle-wave cone) signal. Suprathreshold equiluminant red-green flicker that stimulates the L--M mechanism was presented on a steady, intense yellow-green adapting field. Violet flicker that stimulates the S cones was added to the red-green flicker at different temporal phase angles, and the violet modulation depth was varied to achieve a chromatic discrimination threshold. A template was fitted to the data relating thresholds to phase: the location of the template symmetry axis showed that the S signal lagged L--M by about 75-90 degrees at 10 Hz. This is about one half the phase lag obtained for luminance or motion discrimination. The phase discrepancy shows that there are separate luminance and chromatic mechanisms receiving S cone inputs. The hue of the flicker in the present study varied strongly with phase angle, with the positive and negative excursions of the S cone signal producing a reddish-blue and greenish-yellow, respectively, and these colors combined with the reddish and greenish hues produced by the L--M signal. The observed phase shift, and measured color appearance of the combined flicker, account for the colors seen on a radially segmented disk of Munsell hues when rotated: the colors differ strikingly depending on the direction of rotation.

Adaptation, Ocular↗
PubMed1991

Detection uncertainty and the facilitation of chromatic detection by luminance contours.

A suprathreshold luminance flash (1 degree, 200 msec) on a large uniform yellow field facilitates detection of a coincident (1 degree, 200 msec) red or green equiluminant flash and approximately linearizes the psychometric function for detecting the chromatic flash. The facilitation is produced by the suprathreshold contour created by the luminance flash. We tested whether the contour facilitates detection by reducing spatiotemporal uncertainty in detecting the chromatic flash. Uncertainty increase false alarms, and this effect can be factored out by correcting yes-no psychometric functions for guessing. Uncertainty also alters the shape of the receiver operating characteristic. Measurements of yes-no psychometric functions and receiver operating characteristics do not support the uncertainty reduction hypothesis.

Color Perception↗
PubMed1990

Visual interactions with luminance and chromatic stimuli.

The visibility of a 1 degree, 200-msec flash on a large yellow field was measured as a function of the intensity of a coincident pedestal flash (a flash that was the same in both temporal intervals of a two-alternative forced-choice trial). The various flashes were incremental (+Lum) or decremental (-Lum) yellow luminance flashes or green (+Chr) or red (-Chr) isoluminant chromatic flashes. With uncrossed conditions (Lum tests on Lum pedestals or Chr tests on Chr pedestals), we obtained the conventional dipper function, that is, the function of threshold test intensity was highly asymmetric about zero pedestal intensity, and strong pedestals induced strong masking. Crossed conditions produced neither effect: for example, with Chr tests on Lum pedestals, there was no dipper function: the function of threshold test intensity was symmetric about zero pedestal intensity, and strong pedestals produced no masking. Instead, the suprathreshold luminance pedestals facilitated chromatic detection by as much as 2-3X and also linearized the chromatic psychometric function, further enhancing sensitivity to weak chromatic stimuli. (Chromatic sensitivity on the suprathreshold luminance pedestal was approximately 25X higher than luminance sensitivity on the uniform field.) A pedestal consisting of a thin luminance ring that surrounded the chromatic test produced facilitation equal to that of the uniform-luminance pedestal: the pedestal may thus act to demarcate the test spatially and promote chromatic comparison with the surround. Removing the uniform yellow surround eliminated this crossed facilitation but did not eliminate the uncrossed facilitation (the dipper function), suggesting that different mechanisms mediate the crossed and uncrossed facilitations.

Color↗
PubMed1989

Contribution of human short-wave cones to luminance and motion detection.

1. Human short-wave S cone signals are important for colour vision and here we examine whether the S cone signals also contribute to motion and luminance. 2. Detection was measured with moving patterns that selectively stimulated S cones-violet sine-wave gratings of 1 cycle deg-1 on an intense yellowish field. For rates up to 12 Hz, detection was governed by non-directional mechanisms, possibly of a chromatic nature, as shown by three findings: moving gratings had to be suprathreshold for their direction to be identified; the threshold ratio of counterphase flickering versus moving gratings was low; and direction-selective adaptation was essentially absent. 3. Evidence for less sensitive, directional mechanisms includes the following: at high velocity, the direction of movement of the violet gratings can be identified just slightly above the detection threshold; directional adaptation was strong with a suprathreshold test pattern; velocity was seen veridically for clearly suprathreshold patterns; and a counterphase flickering test, added in spatial-temporal quadrature phase to a similar suprathreshold mask, had identical detection and direction-identification thresholds. 4. Interactions of long-wave L cone and S cone signals in direction-selective mechanisms were measured with an orange counterphase grating and a violet counterphase test, both flickering at the same rate and presented in spatial quadrature phase on the yellowish adapting field. Direction identification thresholds, measured as a function of the temporal phase of two gratings, demonstrated both that the S cone signal lags considerably behind the L cone signal (an effect that strongly varies with S cone light adaptation), and more strikingly, the S cone signal summates with a negative sign and thus is effectively inverted in direction-selective mechanisms. 5. Quantitatively similar temporal phase functions were obtained with uniform violet and orange flicker when a luminance discrimination criterion was used: thus the S cone signal summates negatively with the L cone signal for both discrimination of luminance flicker and the direction of motion. 6. The temporal phase functions accurately predicted threshold summation for identifying the direction of motion of a pair of violet and orange gratings moving with the same velocity but with different spatial phase offsets. Once the relative temporal phase lag of the S cones was compensated for, there was linear threshold summation for the violet and orange patterns when presented in effective (physiological) spatial antiphase, and clear cancellation when presented in phase. This and related experiments show a linear summation of S, M and L cone signals for direction detection, with the S cones having a negative sign.(ABSTRACT TRUNCATED AT 400 WORDS)

Humans↗
PubMed1988

Adaptational effects of short wave cone signals on red-green chromatic detection.

The red-green chromatic detection mechanism that responds to the difference of L and M cone test signals was isolated in forced-choice experiments. Detection contours in an L, M cone space were measured with 2 Hz Gabor test signals comprising different amplitude ratios of antiphase flickering red and green lights, which formed the 1.2 degree center of a 7.2 degree uniform adapting field. To compare the effect of short wave cone adapting levels on the red-green detection sensitivity, thresholds were measured on pairs of adapting fields that were shown to be tritanopic metamers for our individual observers: violet and green adapting lights that produce equal quantal catches in M cones and in L cones but very differently stimulate S cones. The degree to which the adapting field stimulated S cones had little effect on the red-green detection sensitivity, although the red appearance of the adapting field varied considerably owing to the S cone stimulation. Thus, while the S cones may affect the red-green hue dimension, S cone signals appear to have little adaptational effect on red-green detection mediated by the difference of L and M cone test signals.

Adaptation, Ocular↗
PubMed1987

Chromatic suppression of cone inputs to the luminance flicker mechanism.

Eisner and MacLeod [J. opt. Soc. Am. 71, 705-718 (1981)] showed that intense green and red chromatic adapting fields may suppress respectively the M and L cone input to the luminance mechanism by a factor considerably greater than Weber's law. We obtained evidence for such chromatic suppression by measuring complete detection contours for different ratios of red and green test lights presented in rapid flicker in the center of a uniform field. The detection contours represent thresholds as the quantal modulation of the M and L cones normalized by the quantal catch owing to the field. Luminance flicker mechanisms were identified by sections of the contours where detection was controlled by a linear sum of the M and L cone test signals. The slope of these sections indicated that intense red fields selectively suppressed the L cone input to the luminance mechanism by a factor greater than Weber's law; evidence was much less firm for an analogous suppression of the M cone input by intense green fields. The shape of the detection contours also suggests that intense red fields, which differentially light-adapt the M and L cones, may produce a moderate temporal phase-shift between the M and L cone signals. The shape of the temporal MTF of the M cone and the L cone input to the luminance mechanism may be determined at the cone stage, with the absolute sensitivity (vertical scaling) being partially dependent on selective chromatic suppression of the cone inputs owing to the intense chromatic field. Luminance and red-green chromatic temporal sensitivity functions are presented in terms of the M and L cone quantal modulations. Chromatic sensitivity progressively rises above luminance sensitivity as temporal frequency is gradually lowered below 15 Hz, with the consequence that 'contrast sensitivity' may be much higher for color than for luminance.

Adaptation, Ocular↗
PubMed1985

Second-site adaptation in the red-green chromatic pathways.

On different chromatic adapting fields, thresholds were measured with a 1.2 deg flash consisting of simultaneous incremental and decremental red and green components that stimulate the M and L cones in any desired ratio. Thresholds were plotted in normalized coordinates in which the quantal change in the M and L cones due to the flash was divided by the quantal catch due to the field. Detection contours for a wide range of test flashes provide evidence for luminance and chromatic mechanisms that respectively respond to the sum and difference of the M and L cone signals. Field color has little influence on the luminance mechanism but strongly affects chromatic detection, with sensitivity being maximal on yellow fields and declining slightly on green fields and declining strongly on red fields. Similar effects were obtained for long (200 msec) and very brief flashes, although the shape of the contours differed considerably. The results provide evidence for a second adaptation site within the red-green chromatic pathways, similar to the second-site in the S cone pathways. Chromatic fields (green and red) polarize the site and reduce sensitivity to chromatic flashes.

Adaptation, Ocular↗
PubMed1984

Adaptive processes controlling sensitivity of short-wave cone pathways to different spatial frequencies.

The sensitivity of the short-wave cone pathways was measured with violet interference gratings on monochromatic adapting fields. Spectral field sensitivity functions for test gratings of 2, 4 and 8 c/deg approximately matched Stiles' pi 3 function, which presumably reflects light-adaptation of the short-wave cones. Previous work had suggested that field sensitivity varies as a function of test spatial frequency, but this now seems an artifact of spatial adaptation. (The present study shows the pathway is highly susceptible to spatial adaptation induced by fine patterns.) For various spatial frequencies that affect the short-wave pathway, signals also pass through a cancellate adaptation site where signals from the short-wave and the middle- and long-wave cones act in opposition. Transient inputs in either opponent direction polarize or desensitize the opponent site. Additional transient inputs of the opposite sign then reduce the polarization and increase sensitivity. Such effects were demonstrated with test gratings as high as 12 c/deg. Transient effects at the opponent site are particularly evident at higher spatial frequencies.

Adaptation, Ocular↗
PubMed1984

Opponent-movement mechanisms in human vision.

A vertical grating that sinusoidally reverses contrast can be synthesized from two identical component gratings that move with equal velocities in opposite directions (leftward and rightward). Such a counterphase grating is used as a suprathreshold masking pattern. When the mask is of low spatial frequency and is modulated rapidly, a test pattern consisting of an increment of the rightward component and an equivalent simultaneous decrement of the leftward component is highly detectable compared with simultaneous increments or decrements of both components. The visibility of the opponent-movement test signal is strongly facilitated by high-contrast masks. This facilitation is accompanied by a high sensitivity for judging the direction of motion of the test. These results show that certain detection mechanisms are highly sensitive to the difference of the rightward and leftward components. However, when the mask is of threshold contrast, the rightward- and leftward-moving test components appear to be detected independently. A high-contrast grating that rapidly moves in one direction strongly masks gratings moving in the same or opposite direction; this shows that moving patterns are not detected by unidirectional mechanisms when contrast is clearly suprathreshold. The results may be explained by a model with mechanisms that are excited by one direction of motion and inhibited by the opposite direction.

Discrimination Learning↗
PubMed1983

Spatial sensitization and desensitization with small adapting fields: interactions of signals from different classes of cones.

Thresholds for brief, tiny flashes were measured on small adapting fields at 5 degrees retinal eccentricity. Rod influences was eliminated by bleaching. Green and red small adapting fields raised the threshold for a green test flash by stimulating both middle and long wave cones-thus spatial desensitization by small adapting fields is not con-specific. However, a small adapting field that strongly stimulated only short wave cones did not affect the visibility of a long wave flash. Spatial sensitization was also measured, using green or red annuli that surrounded a small red field and green test probe. Sensitization was not cone-specific. Possible mechanisms producing desensitization with small fields and annular sensitization are discussed.

Adaptation, Ocular↗
PubMed1983

The cone threshold: spatial interactions of rod and cone adapting signals.

Steady small blue adapting fields that stimulated only rods produced large threshold elevations for a superimposed tiny red flash that stimulated cones. The threshold elevation differed considerably between observers, confirming the results of Buck (Topical Meeting on Recent Advances in Vision, abstract in Technical Digest, 1980; Invest. Ophthal, visual Sci., Suppl. 20, 207, 1981). A red annulus that stimulated cones reduced slightly the threshold elevation produced by the small rod adapting field. Similarly, when the cone threshold was elevated by a small red field that stimulated only cones, a blue annulus that stimulated rods slightly reduced the threshold of the red cone test flash. These effects, although weak, demonstrate lateral sensitizing interactions between a cone center field and rod annulus, and vice versa, when the cone threshold is assessed with a tiny red flash.

Adaptation, Ocular↗
PubMed1982

Lateral interactions in the control of visual sensitivity.

Threshold vs intensity curves for cone vision, measured in the parafoveal retina, quickly saturate if the adapting background is made small (e.g. 19' at 5 degrees eccentricity). Log increment threshold increases at a rate of about 3:1 with log background illuminance at levels as low as 10 td. This shows that lateral interactions are an important process in preserving differential sensitivity in cone vision across the wide range of illuminances over which it normally operates. Parallels between light and dark adaptation in the effect of field size were explored, since effects of comparable magnitude are observed in both. Backgrounds and bleaches equated for their effects at one field size do not have equal effects on threshold at other field sizes, however, with small-area bleaches raising threshold more than predicted. This failure of equivalence was also revealed in a second experiment, in which recovery of sensitivity following small area bleaches was measured in the presence of large steady background fields, which have the effect of lowering threshold. Thresholds following the small bleach were lowered less than expected on the basis of the "equivalent background" hypothesis, a result which we take to mean that signals from bleached cones exceed those produced by a background which has an equivalent effect on threshold (the "equivalent background"). Control experiments examined whether rods contribute to the overloading of cone response by small fields and the possible contribution of such central adaptation processes as spatial frequency adaptation.

Dark Adaptation↗
PubMed1982

Adaptation to polarized light in humans.

Recent investigators reported large adaptational effects in human vision dependent on the plane of linearly polarized light. In the present study, such adaptational effects were observed to be small or insignificant. Our observers adapted to intense homogenous, foveal fields of linearly polarized, orange-red light produced by a beam that entered the side of the pupil. Periodically the plane of polarization of the beam suddenly shifted 90 degrees without there being any change in the spectral distribution of the light or position of the beam in the pupil plane. The change of radiance of the beam could be adjusted to be as low as approx. 0.5%. Signal detection experiments revealed that observers typically could not detect a change of polarization of the field. Results obtained with the method of adjustment showed that the threshold of an increment flash presented on the intense field was not affected by changing the polarization of the field. Physiological implications of these results are discussed.

Adaptation, Ocular↗
PubMed1982

Low spatial-frequency channels in human vision: adaptation and masking.

Previous work showed that adapting to low spatial frequency gratings (below 1.5 cycles/degree) may cause maximal spatial adaptation at a significantly higher spatial frequency. It has been suggested that there are no adaptable spatial-frequency channels tuned to below 1.5 c/deg. Contrary to this view, we found that adaptation and masking with low spatial frequencies (0.12-1.0 c/deg) produced maximal threshold elevations when the test patterns were the same spatial frequency as the adapting or masking pattern. These results were obtained using test patterns that turned on and off gradually or sharply. The results suggest that there are form mechanisms optimally sensitive to very low spatial frequencies. Adaptation was selective to position (phase) and orientation at low spatial frequencies; masking was observed to be selective to orientation at a spatial frequency as low as 0.2 c/deg. A clear dichotomy between transient, motion channels and sustained, form channels at low spatial and temporal frequencies may represent an unrealistic simplification. There may exist directionally-selective motion mechanisms sensitive to very slow motion, and these may play a role in the discrimination of form. The discussion considers the bandwidths of the low spatial frequency mechanisms.

Adaptation, Ocular↗
PubMed1980

Spatial adaptation of short-wavelength pathways in humans.

Color-selective spatial adaptation of the short-wavelength, or blue-sensitive, pathway was demonstrated. The adaptation was orientation selective and strongly monocular. Adaptation was assessed by measuring visibility thresholds for monochromatic gratings in subjects adapted to high-contrast violet gratings designed to stimulate only blue-sensitive cones. The results showed spatially selective, adaptable channels within the short-wavelength pathway.

Adaptation, Physiological↗