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C F Stromeyer

Publications and source records attributed to C F Stromeyer.

17 recordsLinked to original sources
PubMed1992

Peripheral chromatic sensitivity for flashes: a post-receptoral red-green asymmetry.

Thresholds of luminance and red-green chromatic flashes (200 msec) were measured on a yellow adapting field in the fovea and periphery (up to 12 degrees eccentricity for 1 degree flashes and 21 degrees eccentricity for 2 degrees flashes). Chromatic sensitivity (in cone contrast coordinates) is about 7 times higher than luminance sensitivity in the fovea but falls faster with eccentricity, so that luminance and chromatic sensitivities are similar at eccentricities of 20 degrees or less. At eccentricities greater than about 14 degrees, there is a clear asymmetry wherein green chromatic flashes are considerably less detectable than red ones. By measuring complete detection contours for many ratios of incremental and decremental red and green flashes, we isolated the red and green chromatic detection mechanisms, and demonstrated that the red-green asymmetry is not a property of the L- or M-cone response per se, but rather is a property of the post-receptoral, chromatic mechanisms. The peripheral luminance and chromatic mechanisms could be further separated with a suprathreshold luminance flash (a pedestal), since an intense pedestal masks coincident luminance test flashes but facilitates the chromatic flashes. The luminance pedestal approximately linearizes the chromatic detection function (the psychometric function).

Color Perception↗
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↗
PubMed1979

Response of visual mechanisms to stimulus onsets and offsets.

Transient and sustained visual mechanisms were studied with single, flickering bars of various widths. Wide bars were largely detected on the basis of temporal luminance transients whereas thin bars were detected on the basis of the sustained contrast. A rapidly flickering uniform field selectively masked wide flickering bars, which suggests that different mechanisms detect wide versus thin flickering bars. For coarse spatial patterns, stimulus onsets were slightly more visible than stimulus offsets, and the response to onsets and offsets approximately summated.

Darkness↗
PubMed1978

Apparent saturation of blue-sensitive cones occurs at a color-opponent stage.

Response saturation of blue-sensitive cone pathways was studied by measuring increment thresholds for violet test flashes on flashed violet fields in the presence of a steady yellow "auxiliary" field of constant radiance. Adding intense yellow field flashes to the violet field flash could eliminate or reduce response saturation (greatly reduce threshold), whereas "negative" yellow field flashes drove the mechanism to further saturation. The response saturation is thus not, in general, controlled exclusively by independent blue-sensitive cones but by spectrally opponent mechanisms that receive opposite-signed signals from blue-sensitive cones and from green-or red-sensitive cones. These results add to a growing number of studies that demonstrate that detection of signals from blue-sensitive cones is largely through a color-opponent pathway.

Action Potentials↗
PubMed1978

Spatial-frequency masking with briefly pulsed patterns.

Spatial-frequency masking was studied with briefly pulsed (25 ms) vertical gratings. The mask was a noise grating, and the test pattern was a sinusoidal grating. A low-frequency band of noise masked a low- but not high-spatial-frequency test grating when the patterns were presented simultaneously. A high-frequency band of noise did not mask a low-frequency test grating when the patterns were presented simultaneously or when the mask was presented after the test pattern (backward masking). Masking was, however, observed when the mask or test pattern was of sufficiently high contrast so that the stimuli had nonlinear distortion and thus produced DC shifts of the field luminance.

Humans↗
PubMed1978

Form-colour aftereffects: selectivity to local luminance contrast.

For long periods observers fixated low spatial frequency coloured gratings. Black and white test gratings of the same spatial frequency and orientation as the adapting gratings appeared coloured with the hue complementary to the adapting patterns when the dark test stripes fell on retinal areas previously occupied by the dark adapting stripes; no colour or very weak colour was seen when the test gratings were reversed in phase (contrast reversed). No colour aftereffects were produced with coloured gratings that lacked luminance contrast. The selectivity to the polarity of local luminance contrast can be explained by mechanisms that respond conjointly to colour and luminance contrast. The aftereffects are selective to spatial phase.

Afterimage↗
PubMed1978

Form aftereffect contingent upon a colour shift.

After prolonged fixation of coloured gratings of low spatial frequency, images of the gratings can be elicited up to 90 min thereafter when the colour of a spatially homogeneous test field is suddenly changed. Only adapting gratings with luminance contrast induce clear aftereffects. Control experiments rule out afterimages as an explanation of the aftereffects.

Adaptation, Ocular↗
PubMed1978

Detection of red and green flashes: evidence for cancellation and facilitation.

Green and red flashes of light will differentially stimulate the middle- and long-wavelength sensitive cones. Interaction of cone signals was studied by measuring increment thresholds for combinations of green and red flashes on a yellow adapting field. When the yellow adapting field was at 10.000 trolands (td), green and red incremental flashes (1 degree, 200-msec duration) produced cancellation when presented simultaneously and facilitation when presented sequentially. A green incremental flash (1.15 degrees, 200 msec, 5000-td adaptation field) and red decremental flash, or vice versa, produced facilitation when presented simultaneously. The results can be explained by color-differencing, opponent-mechanisms. The cancellation effect for the simultaneous incremental flashes largely disappeared when the flashes were exposed briefly (10 msec) or reduced in size (0.04 degrees). It is unlikely that the stimuli were exclusively detected by achromatic, luminance channels, as suggested by previous work, since observers could partially distinguish the hue of threshold flashes of 570- and 590-nm light (0.04 degrees, 10 msec) on a bright yellow field.

Color Perception↗