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4-ammonio-2,2,6,6-tétraméthylpipéridinium chromate dihydrate.

The title compound, 4-ammonio-2,2,6,6-tetramethylpiperidinium chromate dihydrate, (C9H22N2)[CrO4]*2H2O, crystallizes in the monoclinic system with one organic cation and one chromate anion in the asymmetric unit, together with three independent sites for water molecules, two of which have their O atoms located on twofold axes. The structure is composed of layers built up from CrO4(2-) tetrahedra and water molecules alternating with C9H22N2(2+) cations and additional water molecules. Two types of hydrogen bonds, O-H...O and N-H...O, ensure the cohesion and stability of the structure.

Journal Article↗

X-ray four-quadrant diamond phase-retarder system to compensate for off-axis and chromatic aberrations.

An X-ray transmission-type double phase-retarder system that can compensate for off-axis aberration (phase-shift inhomogeneity due to angular divergence of incident X-rays) has been developed and its advantage over a conventional single transmission-type X-ray phase retarder was demonstrated. However, it was noticed that the transmission-type X-ray phase retarder suffers from not only off-axis aberration but also chromatic aberration (phase-shift inhomogeneity due to energy spread of incident X-rays). In this paper, a transmission-type X-ray four-quadrant phase-retarder system is proposed that can compensate for both off-axis and chromatic aberrations. The X-ray four-quadrant phase-retarder system is composed of four transmission-type X-ray phase retarders. The scattering planes of four phase-retarder diamond crystals are set to be inclined by 45 degree, 135 degree (= 45 degree + 90 degree), 225 degree (= 45 degree + 180 degree) and 315 degree (= 45 degree + 270 degree), respectively, with respect to the plane of incident polarization. Under the conditions of 7709 eV photon energy, 1.5 eV energy spread and 45" angular divergence (FWHM) of incident X-rays, the X-ray four-quadrant phase-retarder system created 0.98 degree of vertical-linear polarization from horizontal-linear polarization. This value was favorably compared to 0.89 and 0.96, which were obtained by the single and double phase-retarder systems, respectively. The principle of the X-ray four-quadrant phase-retarder system will be described together with its advantage over the single and double phase-retarder systems.

Journal Article↗

Accommodation and chromatic aberration: effect of spatial frequency.

When subjects view an edge in white light, a colour fringe, produced by longitudinal chromatic aberration (LCA) of the eye, is formed at the edge. The colour fringe changes with changes in focus, and serves as a complex colour-coded cue for reflex accommodation. Fincham found that 60% of his subjects failed to accommodate appropriately when the colour fringe was removed with an achromatizing lens or by the use of monochromatic light. Our experiment sought to determine the spatial frequencies at which LCA is most effective. We monitored accommodation in 10 subjects while they viewed sinusoidally moving sine-wave gratings (1-3 D at 0.2 Hz; 1-10.5 c/deg) in a Badal optometer. The targets were 'white' gratings with LCA normal, doubled, neutralized or reversed. Doubling the aberration has minimal effect, removing the aberration reduces gain and increases phase-lag, and reversing the aberration severely disrupts accommodation. Sensitivity to these chromatic cues exists at all spatial frequencies tested, but is most prominent between 3 and 5 c/deg. These results support the view that the system monitors focus by comparing contrast in red-green and perhaps blue-yellow colour-opponent mechanisms.

Accommodation, Ocular↗

Chromatic and luminance losses with multiple sclerosis and optic neuritis measured using dynamic random luminance contrast noise.

We measured thresholds for detecting changes in colour and in luminance contrast in observers with multiple sclerosis (MS) and/or optic neuritis (ON) to determine whether reduced sensitivity occurs principally in red-green or blue-yellow second-stage chromatic channels or in an achromatic channel. Colour thresholds for the observers with MS/ON were higher in the red-green direction than in the blue-yellow direction, indicating greater levels of red-green loss than blue-yellow loss. Achromatic thresholds were raised less than either red-green or blue-yellow thresholds, showing less luminance-contrast loss than chromatic loss. With the MS/ON observers, blue-yellow and red-green thresholds were positively correlated but increasing impairment was associated with more rapid changes in red-green thresholds than blue-yellow thresholds. These findings indicate that demyelinating disease selectively reduces sensitivity to colour vision over luminance vision and red-green colours over blue-yellow colours.

Adult↗

Luminous and chromatic flickering patterns have opposite effects.

When stimulated in phase by a sinusoidally flickering, uniform field, the red and green cone systems tend to inhibit each other. This inhibition is minimized by (i) counterphase (luminance) patterns or (ii) red/green (chromaticity) flicker. However, when (i) and (ii) are combined, the usual flickering-pattern effect is reversed: instead of enhancing chromatic flicker, counterphase patterns tend to suppress it.

Color Perception↗

Similarity of a chromatic adaptation sensor to phytochrome and ethylene receptors.

Complementary chromatic adaptation in cyanobacteria acts through photoreceptors to control the biosynthesis of light-harvesting complexes. The mutant FdBk, which appears black, cannot chromatically adapt and may contain a lesion in the apparatus that senses light quality. The complementing gene identified here, rcaE, encodes a deduced protein in which the amino-terminal region resembles the chromophore attachment domain of phytochrome photoreceptors and regions of plant ethylene receptors; the carboxyl- terminal half is similar to the histidine kinase domain of two-component sensor kinases.

Adaptation, Physiological↗

Chromatic valence curves: alternative interpretation derived by the direct matching method.

The amount of red chromatic valence of the red-green opponent colors channel of the human visual system has been reported to be greatly reduced in short wavelengths when the hue-matching method is used to measure red valence instead of the more typical cancellation method. Receptive fields with a silent surround were postulated to explain the reduction, and it was emphasized that the reduced valence curve represented the true chromatic valence curve of the visual system. In the present studies the previous results are interpreted to be a direct consequence of the method and the particular matching stimuli used. It is shown that the reduction can be explained by the existing color-matching data without appealing to the silent surround hypothesis.

Color Perception↗

Disappearance of stabilized chromatic gratings.

When the image of a stationary, sinusoidal luminance grating is stabilized on the retina of a human subject, he becomes unable to detect this stimulus at contrasts that are readily visible in normal, unstabilized vision. At much higher contrasts, such stabilized gratings can still be seen over most of the normal range of spatial frequencies, although the threshold contrast may be increased by as much as 20 or 30 times. When the analogous experiment is performed with an isoluminance chromatic grating, however, there is no contrast that can restore the visibility of the stabilized grating; the threshold elevations for stabilized chromatic gratings are too great to measure. Saturated red/green gratings fade out and disappear at 100 percent contrast (even where this is 45 times the unstabilized threshold), and they do not reappear as long as stabilization is maintained. Without some kind of temporal variation of the proximal stimulus, the opponent-color pathways apparently do not respond to spatial patterns.

Color↗

Analysis of novel soluble chromate and uranyl reductases and generation of an improved enzyme by directed evolution.

Most polluted sites contain mixed waste. This is especially true of the U.S. Department of Energy (DOE) waste sites which hold a complex mixture of heavy metals, radionuclides, and organic solvents. In such environments enzymes that can remediate multiple pollutants are advantageous. We report here evolution of an enzyme, ChrR6 (formerly referred to as Y6), which shows a markedly enhanced capacity for remediating two of the most serious and prevalent DOE contaminants, chromate and uranyl. ChrR6 is a soluble enzyme and reduces chromate and uranyl intracellularly. Thus, the reduced product is at least partially sequestered and nucleated, minimizing the chances of reoxidation. Only one amino acid change, (Tyr)128(Asn), was responsible for the observed improvement. We show here that ChrR6 makes Pseudomonas putida and Escherichia coli more efficient agents for bioremediation if the cellular permeability barrier to the metals is decreased.

Directed Molecular Evolution↗

Biochemical bases of type IV chromatic adaptation in marine Synechococcus spp.

Chromatic adaptation (CA) in cyanobacteria has provided a model system for the study of the environmental control of photophysiology for several decades. All forms of CA that have been examined so far (types II and III) involve changes in the relative contents of phycoerythrin (PE) and/or phycocyanin when cells are shifted from red to green light and vice versa. However, the chromophore compositions of these polypeptides are not altered. Some marine Synechococcus species strains, which possess two PE forms (PEI and PEII), carry out another type of CA (type IV), occurring during shifts from blue to green or white light. Two chromatically adapting strains of marine Synechococcus recently isolated from the Gulf of Mexico were utilized to elucidate the mechanism of type IV CA. During this process, no change in the relative contents of PEI and PEII was observed. Instead, the ratio of the two chromophores bound to PEII, phycourobilin and phycoerythrobilin, is high under blue light and low under white light. Mass spectroscopy analyses of isolated PEII alpha- and beta-subunits show that there is a single PEII protein type under all light climates. The CA process seems to specifically affect the chromophorylation of the PEII (and possibly PEI) alpha chain. We propose a likely process for type IV CA, which involves the enzymatic activity of one or several phycobilin lyases and/or lyase-isomerases differentially controlled by the ambient light quality. Phylogenetic analyses based on the 16S rRNA gene confirm that type IV CA is not limited to a single clade of marine Synechococcus.

Adaptation, Physiological↗

Vaccinia virus interactions with the cell membrane studied by new chromatic vesicle and cell sensor assays.

The potential danger of cross-species viral infection points to the significance of understanding the contributions of nonspecific membrane interactions with the viral envelope compared to receptor-mediated uptake as a factor in virus internalization and infection. We present a detailed investigation of the interactions of vaccinia virus particles with lipid bilayers and with epithelial cell membranes using newly developed chromatic biomimetic membrane assays. This analytical platform comprises vesicular particles containing lipids interspersed within reporter polymer units that emit intense fluorescence following viral interactions with the lipid domains. The chromatic vesicles were employed as membrane models in cell-free solutions and were also incorporated into the membranes of epithelial cells, thereby functioning as localized membrane sensors on the cell surface. These experiments provide important insight into membrane interactions with and fusion of virions and the kinetic profiles of these processes. In particular, the data emphasize the significance of cholesterol/sphingomyelin domains (lipid rafts) as a crucial factor promoting bilayer insertion of the viral particles. Our analysis of virus interactions with polymer-labeled living cells exposed the significant role of the epidermal growth factor receptor in vaccinia virus infectivity; however, the data also demonstrated the existence of additional non-receptor-mediated mechanisms contributing to attachment of the virus to the cell surface and its internalization.

Animals↗

Corner effect in induced hue: evidence for chromatic band-pass filters.

An experiment is described which investigates the spatial determinants of the apparent difference in hue between the central grey patches of chromatic 'H' pattern pairs, an effect similar to that first demonstrated by Wright (1969, The Measurement of Colour, Hilger, London) in coloured gratings. The hue difference is shown to be analogous to the brightness difference in achromatic 'H' patterns demonstrated by Moulden and Kingdom (1989, Vision Res. 29, 1245-1259). The origin of both effects is argued to be the presence of the corner intersections in the 'H' patterns, which are powerful stimuli for cells with circularly-symmetric, centre-surround organization. It is suggested that the results of the experiment with the chromatic 'H' patterns implicates the operation of cells with a spectrally double-opponent, rather than single-opponent receptive field organization.

Color Perception↗

The local and global processing of chromatic Glass patterns.

Glass patterns are a valuable tool to study the cortical stages of form perception. We use circular Glass patterns (cGP) to study the relation between form and color vision. The detection of Glass patterns is thought to be carried out in at least two stages. In the first stage, the local orientation information from the pairs of dots is analyzed. A later stage integrates this local orientation information to yield the global percept of form. Previous work (K. S. Cardinal & D. C. Kiper, 2003) has shown that the second stage is chromatically selective, with a broad tuning in color space. Here we completed our characterization of the integration stage by measuring the size of the spatial integration area. We find that the integration area is similar to the size of V4 receptive fields. Furthermore, we measured the chromatic selectivity and spatial resolution of the first stage mechanisms. First stage mechanisms are more selective for color than the integration stage. Their spatial resolution is consistent with the idea that V1/V2 neurons perform the analysis of the dot pairs' orientation. Our results are consistent with the idea that V1/V2 neurons perform the local analysis, and that spatial integration is achieved at the level of V4.

Color Perception↗

Contribution of chromatic aberrations to color signals in the primate visual system.

We measured responses to red-green color variation in parvocellular (PC) neurons in the lateral geniculate nucleus of dichromatic ("red-green color blind") marmoset monkeys. Although these animals lack distinct visual pigments to distinguish between wavelengths in this range, many of the colored stimuli nevertheless produced robust responses in PC cells. We show that these responses, which are restricted to high stimulus spatial frequencies (fine image details), arise from chromatic aberrations in the eye. The neural signals produced by chromatic aberrations are of comparable magnitude to signals produced by high-frequency luminance (LUM) modulation and thus could influence cortical pathways for processing of color and object recognition. The fact that genetically "color-blind" primates are not necessarily blind to wavelength-dependent contours in the visual world may have enabled red-green color vision to become linked with high-acuity spatial vision during primate evolution.

Animals↗

Higher level chromatic mechanisms for image segmentation.

We used a noise-masking paradigm to investigate the number and properties of chromatic mechanisms involved in image segmentation. Observers were presented with a pattern of dynamic random squares, each independently modulated along a certain direction in DKL color space, either in the isoluminant plane or in the L - M luminance plane. A signal consisting of a rectangular region of squares, oriented horizontally or vertically, was added to the noise. The signal squares were spatially and temporally aligned to the noise squares, excluding the possibility of phase offsets to mediate segmentation performance. Noise and signal color directions were independently varied, and the signal contrast was measured at which an observer could reliably indicate the orientation of the signal. In a second set of experiments, the noise was simultaneously varying in two directions, symmetrically arranged around the signal direction. Masking was generally highest when signal and noise were modulated along the same direction and minimal for orthogonal noise. No difference was found between signals modulated along cardinal directions or intermediate directions. However, measured tuning widths critically depended on the type of noise: Noise modulated along one direction results in narrow tuning, whereas two-sided noise results in broad tuning. A chromatic detection model with multiple broadly tuned mechanisms successfully accounts for the experimental findings, both for narrow and broad tuning curves. Models with four broadly tuned cardinal mechanisms or multiple narrowly tuned mechanisms failed to reproduce the data. Our results suggest an important role for multiple, broadly tuned mechanisms in image segmentation.

Artifacts↗

Visual performance and subjective discomfort in prolonged viewing of chromatic displays.

Visual search and decision-making performance together with subjective fatigue were investigated over a 4-hr time block as a function of display foreground and background chromaticity using colors matched for brightness. Although some small differences in performance related to chromaticity were observed, these were not exacerbated over time. On the basis of the performance data obtained and the subjective reports, there was no support for the general recommendation to avoid the use of red and blue stimuli, either alone or in combination, in CRT displays.

Asthenopia↗

Chromate-induced epimutations in mammalian cells.

Epigenetic gene silencing by aberrant DNA methylation of gene promoter regions is a nonmutagenic but heritable epigenetic mechanism that may mistakenly cause the silencing of important cancer-related tumor suppressor genes. Using a transgenic, V79-derived, mammalian cell line (G12) that contains a bacterial gpt reporter gene in its DNA, we can study carcinogen-induced gene inactivation by mutagenic as well as epigenetic DNA methylation mechanisms. Whereas numerous carcinogens have previously been shown to be mutagenic in these cells, a few carcinogens, including nickel, diethylstilbestrol, and X-rays, are also capable of silencing the G12 cell gpt transgene by aberrant DNA methylation. Here we report for the first time that carcinogenic potassium chromate salts can also induce aberrant DNA methylation in this system. In contrast insoluble barium chromate produced significant level of mutations in these cells but did not cause DNA methylation changes associated with transgene expression.

Animals↗

Chromatism compensation in wide-band nulling interferometry for exoplanet detection.

We introduce the concept of chromatism compensation in nulling interferometry that enables a high rejection ratio in a wide spectral band. Therefore the achromaticity condition considered in most nulling interferometers can be relaxed. We show that this chromatism compensation cannot be applied to a two-beam nulling interferometer, and we make an analysis of the particular case of a three-telescope configuration.

Journal Article↗