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J S Werner

Publications and source records attributed to J S Werner.

At least 37 records · Page 2Linked to original sources
PubMed1997

Spectral mechanisms of spatially induced blackness: data and quantitative model.

Spectral efficiency functions and tests of additivity were obtained with three observers to identify possible chromatic contributions to spatially induced blackness. Stimuli consisted of a series of monochromatic (400-700 nm; 10-nm steps), 52-arcmin circular test lights surrounded by broadband (x = 0.31, y = 0.37), 63-138-arcmin annuli of fixed retinal illuminance. The stimuli were imaged on the fovea in Maxwellian view as 500-ms flashes with 10-s interstimulus intervals. Observers decreased the intensity of the test center until it was first perceived as completely black. Action spectra determined for two surround levels [2.5 and 3.5 log trolands] had three sensitivity peaks (at approximately 440, 540, and 600 nm), However, when monochromatic surrounds were adjusted to induce blackness in a broadband center, action spectra were unimodal and identical to functions obtained by heterochromatic flicker photometry. Tests of additivity revealed that when blackness is induced by broadband surround into a bichromatic center, there is an additivity failure of the cancellation type. This additivity failure indicates that blackness induction is influenced, in part, by signals from opponent-chromatic pathways. A quantitative model is presented to account for these data. This model assumes that blackness induction is determined by the ratio of responses to the stimulus center and the annulus, and while signals form the annulus are based only on achromatic information, responses from the center are based on both chromatic and achromatic properties of the stimulus.

Color Perception↗
PubMed1996

Long-range interactions in visual perception.

Classical receptive-field concepts have been used to explain local perceptual effects such as border contrast and Mach bands, but are not sufficient to explain global perceptual effects. Examples are the perception of illusory contours, area contrast, color constancy, depth planes, coherent motion and texture contrast. These diverse effects require neurophysiological mechanisms within the visual pathways with long-range interactions. Candidate mechanisms are suggested, including converging feedforward projection to account for the emergence of new response properties at higher levels, recruitment of lateral connections to compensate for loss of afference and explain filling-in, and re-entrant projections from higher levels using synchronization of neuronal responses to account for binding.

Animals↗
PubMed1995

Individual differences in contrast sensitivity functions: longitudinal study of 4-, 6- and 8-month-old human infants.

Contrast sensitivity functions (CSFs) of 25 infants were measured longitudinally at 4, 6 and 8 months of age using a preferential-looking method and the method of constant stimuli. Sine-wave gratings varied from 0.27 to 4.32 c/deg, contained eight unattenuated cycles (with edges tapered to uniform gray), and rose to the desired contrast in 2 sec. (1) The average CSF was described on log-log coordinates by a band-pass function. With development it increased in overall sensitivity to contrast, shifted its peak toward slightly higher spatial frequencies, and increased its high frequency cutoff. (2) Log sensitivity at the CSF peak was slightly higher for female than male infants at 6 months, consistent with the hypothesis that vernier acuity (which also may differ between the sexes at this age) is partly mediated by analyzers tuned to low frequencies. (3) Within age groups the individual differences were such that log sensitivities for neighboring spatial frequencies generally correlated more highly than distant frequencies. With development the correlations among distant frequencies below 1.0 c/deg increased. Monte Carlo simulations of a model that shifts spatial analyzers to higher frequencies with age reproduced these results but simulations of adultlike, unshifting analyzers did not. (4) Measures taken 2 months apart tended to correlate more highly than those taken 4 months apart, though some individual differences in the CSF peak remained stable over 4 months.

Aging↗
PubMed1995

Spectral efficiency measured by heterochromatic flicker photometry is similar in human infants and adults.

Spectral efficiency functions based on heterochromatic flicker photometry (HFP) were measured for three adults and 42 infants using a rapid visually-evoked potential (VEP) method. A 5 degrees-diameter, broadband standard (0.6 cd/m2) was presented in square-wave counterphase (15 Hz) with one of 13 monochromatic lights (420-660 nm; 20 nm steps). The intensity of the monochromatic light was continuously varied while extracting the phase-locked VEP amplitude of the fundamental component. HFP functions measured psychophysically by the method of adjustment were also obtained for the adults. Adult HFP functions from the two methods were found to be essentially the same. Both of these functions were compared to Vos'-modified 2 degrees V(lambda) function and the 10 degrees CIEV(lambda) function. The mean adult data were slightly better fit to the 2 degrees V(lambda) function than to the 10 degrees CIEV(lambda) function, although there was an elevation in sensitivity at 420 and 440 nm. Infant HFP functions were similar to Vos' modified V(lambda) except for an elevation in efficiency at short wavelengths. The mean infant HFP function agreed better with the 10 degrees CIEV(lambda) function than Vos'-modified V(lambda) function, but infant sensitivity was elevated by 0.4 log units at 420 nm compared to the 10 degrees CIE observer. The elevation found at short wavelengths for both adults and infants is attributed to individual and age-related variation in the density of the ocular media, and to reduced macular pigment screening resulting from use of a 5 degrees field size.(ABSTRACT TRUNCATED AT 250 WORDS)

Adult↗
PubMed1995

Contributions of neural pathways to age-related losses in chromatic discrimination.

Chromatic-discrimination thresholds were measured for light mixtures lying along individually determined tritan axes and an axis of constant short-wavelength-sensitive- (S-) cone stimulation for 30 color-normal observers (age range 22-77 years). The stimulus was a foveally viewed 2 degrees, circular bipartite field consisting of a standard and a test light. Heterochromatic flicker photometry was used to equate the retinal illuminance of the stimuli at 120 Td for all observers. All stimuli were presented in Maxwellian view. Age-related losses in chromatic discrimination depended on the level of cone stimulation. At relatively lower levels of S- and long-wavelength-sensitive (L-) cone stimulation, discrimination thresholds were elevated for older relative to younger observers. As the level of simulation increased for these two cone types, thresholds converged, on average, for all observers. Application of a model of chromatic discrimination mediated by an S-cone pathway suggests that there is no significant age-related change in Weber fractions and that age-related losses in chromatic discrimination are due, at least in part, to spontaneous neural noise arising in the pathway and/or neural changes that multiplicatively scale all incident light.

Adult↗
PubMed1994

Effect of cataract surgery on contrast sensitivity and glare in patients with 20/50 or better Snellen acuity.

The effect of cataract surgery was assessed in 103 patients whose visual acuity, as measured in dim light and with high contrast Snellen letters, was 20/50 or better. The patients desired cataract surgery. They complained of glare symptoms, had given up driving at night, or both. Contrast sensitivity was measured under simulated night conditions with a calibrated Vistech MCT 8000 device. No patient who had a contrast sensitivity of less than 27 at 6 cycles per degree (20/70 "equivalent acuity") had cataract surgery. The mean preoperative contrast sensitivity function showed abnormally low values for all frequencies (cycles/degree) tested. Postoperatively the values returned to normal. Of 99 patients who answered a postoperative questionnaire, 41 (41%) had been driving at night preoperatively and 80 (80%) were driving at night postoperatively. A control group of 24 noncataractous patients (48 eyes) was in the normal range of the test device used. These results support the view that the benefits of cataract surgery are not well predicted by Snellen acuity, even though functional vision may be significantly reduced.

Aged↗
PubMed1994

Spectral efficiency across the life span: flicker photometry and brightness matching.

Spectral efficiency functions were measured for 50 color-normal observers (aged 19-85 years) by means of heterochromatic flicker photometry (HFP) and heterochromatic brightness matching (HBM). Foveally viewed, circular, 1.2 degrees-diameter stimuli were presented as 3-s flashes (50% duty cycle) in Maxwellian view. Monochromatic lights (420-700 nm; 16 wavelengths) were equated to a 100-Td (trolands), broadband white standard in both procedures. In both HFP and HBM, average sensitivity (specified at the cornea) decreased at short wavelengths with increasing age, consistent with age-related increases in the density of the ocular media. The short-wavelength HBM decline was of lower magnitude than the HFP decline. HFP data were modeled by a weighted additive combination of long- and middle-wavelength-cone inputs and density spectra of the ocular media and macular pigment. HBM data were analyzed with an upper envelope of additive and subtractive combinations of log-transformed cone absorption functions. These analyses indicated that HBM sensitivity, specified at the retina by correction for estimated lens and macular pigment density, increased with age in an approximately wavelength-independent manner over a broad range from 420 to 560 nm.

Adult↗
PubMed1993

Individual differences in contrast sensitivity functions: the first four months of life in humans.

Contrast sensitivity functions of forty 4-month-old human infants were measured using a preferential-looking method and the method of constant stimuli. Circular sinewave gratings varied from 0.27 to 1.08 c/deg, contained eight unattenuated cycles (with edges tapered to uniform gray), and rose to the desired contrast in 2 sec. Log contrast sensitivities for variables close in spatial frequency correlated more highly than those that were farther apart in these data, and in data of 1-, 2-, and 3-month-olds from Banks and Salapatek [(1981) Journal of Experimental Child Psychology, 31, 1-45]. Factor analyses yielded at least two frequency-tuned factors per age group. Monte Carlo simulations of a quantitative model that shifts spatial mechanisms to higher frequencies with age reproduced the results for 4-month-olds, but simulations of adultlike, unshifting mechanisms did not. The data are consistent with the following conclusions: (a) individual differences in the sensitivity of spatial mechanisms may explain some individual differences in CSFs; (b) factor analysis may help to estimate mechanism tuning; and (c) spatial mechanisms may shift to higher frequencies during development.

Contrast Sensitivity↗
PubMed1993

Loci of achromatic points throughout the life span.

Mixtures of monochromatic lights that appear achromatic were measured for 50 normal, trichromatic observers ranging in age from 11 to 78 years. Stimuli were presented to one eye as a 1 degree-diameter, 1-s flash (10-s interstimulus interval) in Maxwellian view. We found the achromatic locus by varying the intensity ratio of each observer's spectral unique blue and unique yellow while maintaining constant overall retinal illuminance. Measurements were made for three levels of retinal illuminance (10, 100, 1000 trolands). Additional verification of the position of the achromatic locus in color space was obtained for 23 subjects with the use of a mixture composed of 600-nm light and its spectral complement. There were no significant changes in the achromatic loci as a function of age. The mean achromatic locus in CIE chromaticity space was x, y = 0.31, 0.31 or u',v' = 0.21, 0.46. These results suggest that partial compensation for age-related changes in visual mechanisms occurs in a way that preserves constancy of the achromatic locus across the life span.

Adolescent↗
PubMed1992

Sites of age-related sensitivity loss in a short-wave cone pathway.

The age-related losses in the sensitivity of a short-wave (S) cone mechanism were determined by measuring the threshold-versus-radiance (t.v.r.) functions for nine older (mean age, 71.0 years) and six younger (mean age, 24.4 years) subjects. Measurements were obtained for a 250-ms, 1.03 degrees-diameter, 440-nm foveally viewed test light presented on 470-nm adapting fields and on a 570-nm auxiliary field. A comparison of t.v.r. functions revealed intensity-dependent sensitivity losses in the older group. By applying a quantitative model of an S-cone pathway to the t.v.r. data obtained from the older subjects, we found that the age-related changes in the ocular media and the receptor sensitivities can account for much but not all of the difference in the sensitivity of an S-cone mechanism demonstrated by eight of our nine older subjects.

Adolescent↗
PubMed1991

The invariance of unique white; a possible implication for normalizing cone action spectra.

The locus of unique white was measured for two observers over a wide range of stimulus intensities, using both direct matching and absolute judgements. Chromaticity coordinates of each observer's unique white were found to be invariant over a range of about 4 log units. This result is discussed in the context of the class of models that explain the intensity-evoked change in perceived color (Bezold-Brücke effect) on the basis of response compression in color channels. Invariance of unique white may be interpreted, then, as evidence for its non-polarizing effect on color channels, including the three classes of cones. On the basis of that assumption we have used unique white as criterion for normalizing cone action spectra. Assuming an equal-energy spectrum for the standard observer's unique-white stimulus, as we found to be consistent with literature data, we calculated the associated coefficients of the conversion formulae between CIE space and cone space (both for XYZ to LMS and LMS to XYZ) of the Vos-Walraven (1971 Vision Research, 11, 799-818) and Smith-Pokorny (1975 Vision Research, 15, 161-171) receptor fundamentals. The action spectra that thus result, intersect at the spectral neutral (achromatic) points of the three classes of dichromats.

Color Perception↗
PubMed1991

Children's sunglasses: caveat emptor.

Spectrophotometric measurements were obtained on 40 pairs of children's sunglasses. Some of these sunglasses provide excellent protection from the potentially damaging effects of ultraviolet radiation (UVR), whereas others fail to provide adequate protection for the crystalline lens and retina. Some labels were ambiguous and misleading with respect to whether the sunglass provided adequate absorption of UVR.

Child↗
PubMed1990

Light, vision, and aging.

Recent research on aging of chromatic and spatial vision processes is reviewed. Changes in these visual processes with advancing age are largely continuous. Age-related declines in visual performance may be explained in terms of reductions in the illuminance of the visual stimulus due to changes in the ocular media and losses of efficiency at a neural level. Thus, some prominent characteristics of the senescent visual system are similar to those of the younger visual system operating at a lower ambient light level. One important determinant of retinal aging may be the light history of the individual, i.e., cumulative exposure to high-energy photons from solar radiation may accelerate retinal aging. If these abstractions from the literature are valid, then it will become more important to control the light environment throughout the life span.

Aged↗
PubMed1990

Additivity of spatially induced blackness.

Tests of additivity of the postreceptoral pathways that mediate the perception of blackness were conducted under conditions of spatial contrast. Observers increased the radiance of a surrounding annulus until a broadband (white) test center appeared completely black. Additivity tests with heterochromatic flicker photometry (HFP) and direct brightness matching were also conducted for each observer. The results indicated that the luminance level of the annulus required to induce blackness did not change with variations in spectral composition. Results consistent with additivity were also obtained for HFP, but the results from brightness matching were not consistent with additivity. The data support the view that the perception of blackness is mediated by neural mechanisms that additively combine the input of middle- and long-wave photoreceptors.

Adult↗
PubMed1990

Loci of spectral unique hues throughout the life span.

Spectral unique hues (blue, green, and yellow) were determined for 50 observers ranging in age from 13 to 74 years. Each unique hue was measured at three luminance levels (0.5-log-unit steps). There were no significant changes in the spectral locations of red-green equilibrium hues (unique blue and yellow) as a function of luminance level or age. In contrast, significant shifts in unique green loci occurred as a function of both age and luminance. Unique green loci shifted toward shorter wavelengths with age. These results are consistent with the hypothesis that with advancing age there is a parallel decline in the input of all three cone types to the red-green chromatic channel and either a selective decline in short-wave-sensitive cone input to the yellow-blue chromatic channel or a change in the way in which cone signals are combined within the yellow-blue channel.

Adolescent↗