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PubMed1988

Illusory contours induced by isoluminant chromatic patterns.

An illusory-contour was induced by abutting colored gratings embedded in the white field under isoluminance condition. The present study specified the stimulus conditions that invoked the just-perceptible illusory contours for the isoluminant chromatic patterns. The results showed that the purity difference between the colored lines and the white field required for the illusory-contour perception gave a function closely resembling in shape the function obtained for saturation discrimination. Increasing the width of lines reduced threshold for the perception of illusory contours, while the line spacing had no significant effect. The dependence of the illusory-contour perception upon saturation could be accounted for by considering the extraction of the edge and colour information by means of the opponent-color processes observed for the cells in the retina and LGN. On the other hand, the effects of the spatial parameters met the response properties observed for the cells in the visual cortex. It is suggested that the perception of illusory contour may result from hierarchical organization from the retina to cortex in the visual system.

Color Perception↗
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↗
PubMed1989

Chromatic opponency in 3-month-old human infants.

A test spectral sensitivity curve was measured on 3-month-old human infants using a steady 8 degrees test light on a 580 nm adapting field. The data show a "Sloan" notch near 580 nm and a peak near 610 nm. The results are compared to standard nonopponent and opponent models of color vision, and it is concluded that 3-month-old infants have a chromatically opponent detection channel.

Adaptation, Ocular↗
PubMed1990

Salience of chromatic basic color terms confirmed by three measures.

Using single color terms of their choice, nine subjects named each of 424 colors twice under carefully-controlled conditions. Compared to any other color names, the chromatic basic color terms (red, green, yellow, blue, orange, purple, brown and pink) are all used more consistently within subjects, with greater consensus between subjects, and with shorter mean response times; there is no overlap between the two categories of color names by any of these criteria. The results are interpreted as supporting the conception that basic color terms refer to fundamental sensations for which there is a specific physiological basis.

Adult↗
PubMed1991

The contribution of chromatic and achromatic valence to spectral saturation.

The spectral efficiency of the achromatic and opponent chromatic channels was measured in three subjects by use of heterochromatic flicker photometry and hue cancellation, respectively. Heterochromatic brightness matching was also used for measuring achromatic spectral efficiency. These data were then used to predict spectral saturation based on Hurvich and Jameson's (1957; Psychological Review, 64, 384-404) opponent colors model. A standard color-naming procedure and a saturation matching technique were used for measures of spectral saturation. The ratio of saturation of short-wave to long-wave lights was found to be less than that predicted by the linear valence model. Allowing for nonlinearity at the opponent site of the yellow-blue channel plus a desaturating signal from the rods provided a good fit between data and theory.

Adult↗
PubMed1992

Spectral sensitivities for illusory contour perception: a manifold linkage of chromatic and achromatic cues with the generation of contours.

Using colored inducing patterns presented as increments upon a white uniform background, the increment thresholds needed for illusory contour perception were measured as a function of the wavelength of inducing pattern. The spectral sensitivity functions were obtained with varying adaptation level and stimulus configuration, high and low background illumination, and line-based and figure-based inducing patterns. The results showed a distinctive feature between the line-based and the figure-based illusory contours. The sensitivity functions for the line-based illusory contours showed the characteristics of non-opponent mechanisms and they were shape invariant with background intensity and spatial variables. On the other hand, the sensitivity functions for the figure-based illusory contours showed non-opponent nature for low background illumination but opponent nature for high background illumination. It is suggested that the generation of illusory contours involves concurrent processing of different cues of luminance and color, and that photopic adaptation level and stimulus configuration control the degree of the contributions of chromatic and achromatic mechanisms to contour formation.

Adaptation, Ocular↗
PubMed1996

Perceived velocity of luminance, chromatic and non-fourier stimuli: influence of contrast and temporal frequency.

We measured perceived velocity as a function of contrast for luminance and isoluminant sinusoidal gratings, luminance and isoluminant plaids, and second-order, amplitude-modulated, drift-balanced stimuli. For all types of stimuli perceived velocity was contrast-invariant for fast moving patterns at or above 4 deg/sec. For slowly moving stimuli the log of perceived velocity was a linear function of the log of the contrast. The slope of this perceived velocity-vs-contrast line (velocity gain) was relatively shallow for luminance gratings and luminance plaids, but was steep for isoluminant gratings and isoluminant plaids, as well as for drift-balanced stimuli. Independent variation of spatial and temporal frequency showed that these variables, and not velocity alone, determine the velocity gain. Overall, the results indicate that slow moving stimuli defined by chromaticity or by second-order statistics are processed in a different manner from luminance defined stimuli. We propose that there are a number of independent mechanisms processing motion targets and it is the interplay of these mechanisms that is responsible for the final percept.

Color Perception↗
PubMed1995

Development of chromatic discrimination in early infancy.

Combining a habituation-recovery paradigm with procedures to minimize brightness cues, we evaluated 1-3-month-olds' ability to discriminate among broadband mid- and long-wavelength stimuli. One-month olds showed evidence of discriminating a red (dominant lambda = 650 nm) from green (dominant lambda = 545 nm) but failed to discriminate either of these from a yellow (dominant lambda = 585 nm). At 2 months, infants showed evidence of discriminating 545-nm green from 585-nm yellow, but only at 3 months do they appear to discriminate 650-nm red from the yellow. Consistent with previous work, these data imply that chromatic discrimination emerges slowly over the first three postnatal months. Moreover, the developmental pattern is consistent with the notion that early human vision is limited by general rather than selective immaturities within the requisite retinal and neural mechanisms.

Color Perception↗
PubMed2004

Orientational contrast sensitivity and chromatic contrast thresholds in multiple sclerosis.

PURPOSE: To investigate abnormalities of orientational contrast sensitivity (CS) and chromatic contrast threshold (CCT) in multiple sclerosis (MS). DESIGN: Case control study. METHODS: Nine subjects (mean age, 42 +/- 11 years; range, 20-62 years) with MS, an expanded disability status scale of 3 or less, and normal visual acuity (VA) (logarithm of the minimum angle of resolution [logMAR] VA less than.1) in the tested eye were age-matched with 20 controls. Achromatic CS and CCT were measured using static, computer-generated sinusoidal gratings displayed on a high-resolution monitor. The CS and CCT of each subject were determined using a randomized double-staircase reversal algorithm; CS was measured at five spatial frequencies with horizontal orientation and three with vertical orientation; CCT was measured along the red-green and tritan confusion axes. The sensitivity thresholds of subjects were examined in relation to the mean sensitivity of controls for each spatial frequency. RESULTS: Two subjects had loss of horizontal and vertical CS, and three had isolated vertical loss. When compared with the control mean, there were significant reductions in red-green (P =.016) and tritan (P =.016) discrimination thresholds. CONCLUSION: This study used a computerized psychophysical test designed to minimize many of the test errors associated with earlier studies. It provides confirmatory evidence that MS may be associated with a loss of orientational CS and color vision, in the absence of reduced VA.

Adult↗
PubMed2006

Evaluating landfill disposal of chromated copper arsenate (CCA) treated wood and potential effects on groundwater: evidence from Florida.

Chromated copper arsenate (CCA) treated wood has been used for more than 50 years. Recent attention has been focused on appropriate disposal of CCA-treated wood when its service life ends. Groups in the US and Europe concerned with the possibility of arsenic migration to groundwater from disposed CCA-treated wood have proposed that consumers be required to dispose of the wood as a hazardous waste, in the most protective of landfills. We examined available data for evidence of arsenic migration from unlined construction and demolition (C&D) debris landfills in Florida, where CCA-treated wood is disposed. Florida was chosen because soil, groundwater, landfill design, weather, and levels of CCA-treated wood use make the state a uniquely sensitive indicator for observing arsenic migration from CCA-treated wood disposal sites, should it occur. We developed and quality-checked a CCA-treated wood disposal model to estimate the amount of wood and associated arsenic disposed. By 2000, an estimated 13 million kg of arsenic in CCA-treated wood was disposed in Florida; however, groundwater monitoring data do not indicate that arsenic is migrating from unlined C&D landfills. Our results provide evidence that highly stringent regulation of CCA-treated wood disposal, such as treatment as a hazardous waste, is unnecessary.

Arsenates↗
PubMed2005

Review of disposal technologies for chromated copper arsenate (CCA) treated wood waste, with detailed analyses of thermochemical conversion processes.

Several alternative methods for the disposal of chromated copper arsenate (CCA) treated wood waste have been studied in the literature, and these methods are reviewed and compared in this paper. Alternative disposal methods include: recycling and recovery, chemical extraction, bioremediation, electrodialytic remediation and thermal destruction. Thermochemical conversion processes are evaluated in detail based on experiments with model compounds as well as experimental and modelling work with CCA treated wood. The latter category includes: determination of the percentage of arsenic volatilised during thermal conversion of CCA treated wood, identification of the mechanisms responsible for arsenic release, modelling of high temperature equilibrium chemistry involved when CCA treated wood is burned, overview of options available for arsenic capture, characterisation of ash resulting from (co-)combustion of CCA treated wood, concerns about polychlorinated dibenzo-p-dioxins/furans (PCDD/F) formation. Finally, the most appropriate thermochemical disposal technology is identified on short term (co-incineration) and on long term (low-temperature pyrolysis or high-temperature gasification).

Air Pollutants↗
PubMed2006

Leaching of chromated copper arsenate (CCA)-treated wood in a simulated monofill and its potential impacts to landfill leachate.

The proper end-of-life management of chromated copper arsenate (CCA)-treated wood, which contains arsenic, copper, and chromium, is a concern to the solid waste management community. Landfills are often the final repository of this waste stream, and the impacts of CCA preservative metals on leachate quality are not well understood. Monofills are a type of landfill designed and operated to dispose a single waste type, such as ash, tires, mining waste, or wood. The feasibility of managing CCA-treated wood in monofills was examined using a simulated landfill (a leaching lysimeter) that contained a mix of new and weathered CCA-treated wood. The liquid to solid ratio (LS) reached in the experiment was 0.63:1. Arsenic, chromium, and copper leached from the lysimeter at average concentrations of 42 mg/L for arsenic, 9.4 mg/L for chromium, and 2.4 mg/L for copper. Complementary batch leaching studies using deionized water were performed on similar CCA-treated wood samples at LS of 5:1 and 10:1. When results from the lysimeter were compared to the batch test results, copper and chromium leachability appeared to be reduced in the lysimeter disposal environment. Of the three metals, arsenic leached to the greatest extent and was found to have the best correlation between the batch and the lysimeter experiments.

Arsenates↗
PubMed2004

Acclimation of Haslea ostrearia to light of different spectral qualities - confirmation of 'chromatic adaptation' in diatoms.

The marine diatom Haslea ostrearia was cultured under light of different qualities, white (WL), blue (BL), green (GL), yellow (YL), red (RL), and far-red (FRL) and at two irradiance levels, low and high (20 and 100 micromolphotonsm(-2)s(-1), respectively). The effects of the different light regimes were studied on growth, pigment content, and photosynthesis, estimated by the modulated fluorescence of chlorophyll, as relative electron transport rate (rETR). For all the light qualities studied, growth rates were higher at high irradiance. Compared to the corresponding WL controls, growth was higher in BL and lower in YL at low irradiance, and lower in YL and GL at high irradiance. Except for YL, almost all the pigment contents of the cells were lower at high irradiance. At low irradiance, cell pigment contents (chlorophyll a and c, fucoxanthin) and pigment ratios (in function of chlorophyll a) were lower in YL, RL, and FRL. Whatever the irradiance level, the maximum PSII quantum efficiency (F(v)/F(m) remained almost constant for WL, BL, and GL. Other fluorescence parameters (photochemical quenching, rETR(max), and alpha, the maximum light utilization coefficient) were lower in GL, YL, RL, and FRL, at low irradiance. Although not statistically significant, BL caused an increase in these fluorescence parameters. These findings are interpreted as evidence that inverse chromatic acclimation occurs in diatoms.

Acclimatization↗
PubMed2006

Chromatic aberration and the roles of double-opponent and color-luminance neurons in color vision.

How does the visual cortex encode color? I summarize a theory in which cortical double-opponent color neurons perform a role in color constancy and a complementary set of color-luminance neurons function to selectively correct for color fringes induced by chromatic aberration in the eye. The theory may help to resolve an ongoing debate concerning the functional properties of cortical receptive fields involved in color coding.

Animals↗
PubMed2004

The addition of chromatic aberration coefficients.

The asymptotic chromatic aberration coefficients of electron lenses may be written as polynomials in reciprocal magnification. Expressions for the polynomial coefficients of a doublet are derived in terms of those of the individual members of the doublet.

Journal Article↗
PubMed2004

Compensation for longitudinal chromatic aberration in the eye of the firefly squid, Watasenia scintillans.

The camera eyes of fishes and cephalopods have come forth by convergent evolution. In a variety of vertebrates capable of color vision, longitudinal chromatic aberration (LCA) of the optical system is corrected for by the exactly tuned longitudinal spherical aberration (LSA) of the crystalline lens. The LSA leads to multiple focal lengths, such that several wavelengths can be focused on the retina. We investigated whether that is also the case in the firefly squid (Watasenia scintillans), a cephalopod species that is likely to have color vision. It was found that the lens of W. scintillans is virtually free of LSA and uncorrected for LCA. However, the eye does not suffer from LCA because of a banked retina. Photoreceptors sensitive to short and long wavelengths are located at appropriate distances from the lens, such that they receive well-focused images. Such a design is an excellent solution for the firefly squid because a large area of the retina is monochromatically organized and it allows for double use of the surface area in the dichromatically organized part of the retina. However, it is not a universal solution since compensation for LCA by a banked retina requires that eye size and/or spectral separation between photopigments is small.

Animals↗
PubMed2004

Chromatic induction in humans: how are the cone signals combined to provide opponent processing?

We investigated the effect of 16 isoluminant chromatic surrounds on the perceived colour of an enclosed grey test-field at photopic (43 cd/m2) conditions. Stimuli were shown on a grey background identical to the test-field. Use of these stimuli implies that activations of receptoral (cS, cM, and cL) and postreceptoral (cM-cL, cS-(cM+cL)) mechanisms by surround colours are known quantitatively. This allows to predict shifts in colour of the test-field in terms of receptoral (adaptation) as well as postreceptoral (contrast) mechanisms assuming a standard two-stage model. Predictions are tested using matching and hue compensation procedures. Both procedures yield comparable results that are consistent with the assumption that postreceptoral mechanisms explain the observed shifts in perceived colour.

Adaptation, Physiological↗
PubMed2004

Is the S-opponent chromatic sub-system sluggish?

The S-opponent pathway has a reputation for being sluggish relative to the L/M-opponent pathway. Cottaris and De Valois [Nature 395 (1998) 896] claim that S-opponent signals are available in Macaque V1 only after 96-135 ms whereas L/M-opponent signals are available after 68-95 ms. Our experiments tested whether this large latency difference could be observed psychophysically. We measured reaction times to S/(L + M) and L/(L + M) increments. Both the equiluminant plane and the tritan line were empirically determined and we used spatio-temporal luminance noise to mask luminance cues. An adaptive staircase progressed according to observers' performance on a 'go, no-go' task and provided concomitant estimates of threshold and of reaction time. When brief stimuli are confined to chromatic channels and presented at equivalent (threshold) levels and when latency is estimated from visually triggered reaction times, we find that the difference between the L/M-opponent and S-opponent sub-systems is, at most, 20-30 ms.

Color Perception↗