Biomedical subjects

R L Vimal

Publications and source records attributed to R L Vimal.

9 recordsLinked to original sources

PubMed2000

Spatial color contrast matching: broad-bandpass functions and the flattening effect.

The contrast matching function (CMF) is the reciprocal of test contrast that perceptually matches the contrast of standard pattern, measured as a function of test spatial frequency (SF). Achromatic CMFs usually flatten as the contrast of the standard is raised, and are broader than the achromatic, bandpass, contrast sensitivity function (CSF). This report investigates whether chromatic CMFs have similar characteristics. For this purpose, the red-green color channel was defined using minimum flicker and hue cancellation techniques. Spatially localized (D6), vertical, equiluminant patterns (SFs: 0.063-8 cpd; contrast: 3-80%) were used to measure the CSF and CMF of isoluminant patterns presented with a temporal Gaussian envelope. CMFs were measured using a randomized double-staircase procedure and the two-interval forced choice technique. Two color-normal observers, whose task was to select the interval that had higher color contrast, participated in experiments. Results show that: (a) the color CMFs are lowpass functions of SF at low standard contrasts (3-12.5%), broad-bandpass at intermediate contrasts (6.25-60%), and near-flat at high contrasts (80%); and (b) isoluminant CMFs have higher upper cut-off frequencies than isoluminant CSFs. It is concluded that: (i) color-contrast-constancy (CMF independent of SF) is partly achieved at high contrasts because color CMFs flatten as contrast increases; (ii) the information processing at suprathreshold levels is different from that at the threshold levels; and (iii) the model that explained achromatic CMFs using achromatic threshold mechanisms could not explain chromatic CMFs using chromatic threshold mechanisms.

Adult↗

PubMed1998

Spatial-frequency tuning of sustained nonoriented units of the red-green channel.

The existence of nonoriented cells but not of sustained orthogonal masking for achromatic stimuli led to an investigation of the spatial-frequency (SF) tuning of sustained nonoriented color units. For this purpose the Red-Green channel was isolated by the minimum flicker and hue cancellation techniques. Chromatic contrast sensitivity functions (CSF's), threshold elevation (TE) curves, and contrast nonlinearities (TE-versus-mask-contrast curves) were measured with spatially localized vertical color tests and sinusoidal orthogonal color masks by the method of constant stimuli under Gaussian temporal presentation. Results show that (1) color CSF's are a low-pass function of SF, whereas TE curves are a bandpass function of mask SF, and (2) a minimum of six SF-tuned color mechanisms (one low pass and five bandpass functions of SF, with peak SF's of 0.13, 0.5, 2, 4, and 8 cycles per degree and bandwidths of 3.9, 4.4, 2.9, 2.1, 1.1, and 1.2 octaves), similar to oblique-masking color mechanisms, are extracted by the multiple-mechanisms model. These data imply that (1) most of the SF tuning of the broadly oriented color units is already present in the circularly symmetric units, and (2) the latter may be an input to the former.

Color↗

PubMed1998

Color-luminance interaction: data produced by oblique cross masking.

Threshold-elevation (TE-) versus-mask-spatial-frequency (SF) curves and TE-versus-mask-contrast curves, produced by the oblique-masking technique, were reported for uncrossed stimuli (color-test-on-color-mask and luminance-test-on-luminance-mask) [Invest. Ophthalmol. Visual Sci. Suppl. 34, 751 (1993) and Vision. Res. 23, 873 (1983)]. The technique minimizes the artifacts that are due to spatial phase effects, spatial beats, spatial probability summation, and local cues. My goal was to measure these curves for crossed stimuli (color-test-on-luminance-mask and luminance-test-on-color-mask) by this oblique-masking technique and to compare the curves with those reported in previous studies. For this purpose threshold contrasts were measured by a yes-no procedure with randomized double staircases. Test targets were vertical spatially localized (D6) patterns, and masks were oblique sinusoidal patterns; both the test and the mask were presented simultaneously, for 2 s (Gaussian window), on a color monitor interfaced with an ATVista system and a Powell achromatizing lens. The test SF's were 0.125, 0.5, 2, 4, and 8 cycles per degree (cpd); mask SF's were 0.031-16 cpd; and mask contrasts were 6.25%-50%. Furthermore, the Red-Green channel was defined by the minimum flicker and the hue cancellation techniques. Results show mostly masking effect (TE > 1) at contrasts above threshold; sometimes, separability (TE = 1) and above-threshold facilitation (TE < 1) effects were also observed, depending on the test SF, the mask SF, the mask contrast, and the subject. In general, the magnitudes of TE's are smaller and the TE-versus-mask-SF curves are slightly narrower for the oblique-cross-masking conditions than those for the respective oblique uncross masking. In addition, the TE-versus-mask-contrast curves for the crossed conditions are mostly shallower than those for the respective uncrossed conditions. Furthermore, mostly the color-luminance asymmetry (color masks luminance more than luminance masks color) is found, in mild form, for SF's > or = 0.5 cpd. For the lower SF of 0.125 cpd, there is either a lack of asymmetry or a very mild asymmetry of the opposite kind (luminance masks color slightly more than color masks luminance) seems to prevail. In general, the oblique-masking data shows mild asymmetry and reduced facilitation; both are consistent with reduced local cues, similar to those shown by randomized phase data, thus making the data suitable for SF analysis; moreover, at high contrast, the masking data are consistent with those reported in previous studies.

Adult↗

PubMed1995

Effects of eye position on auditory localization and neural representation of space in superior colliculus of cats.

The maps of visual and auditory space within the superior colliculus are in approximate register both with each other and with the underlying motor maps associated with orienting responses. The fact that eyes and ears can move independently poses a problem for the sensorimotor organization of these two modalities. By monitoring eye and pinna positions in alert, head-fixed cats, we showed that the accuracy of saccadic eye movements to auditory targets was little affected by eye eccentricity (range +/- 15 deg) at the onset of the sound. A possible neural basis for this behavioral compensation was suggested by recordings from superior colliculus neurons. The preferred sound directions of some neurons in the deep layers of this midbrain nucleus exhibited a shift with the direction of gaze, while in others the response throughout the auditory receptive field was either increased or decreased, suggesting that changes in eye position alter the gain of the auditory response.

Acoustic Stimulation↗

PubMed1989

Foveal cone thresholds.

The method of constant stimuli was used to estimate the psychometric functions for detection of one or two flashes when two light pulses were presented. The test stimulus consisted of two simultaneous 0.5 msec, 1' pulses separated by 17'. Observers reported seeing 0, 1 or 2 flashes. A computer-controlled direct-view apparatus allowed sampling of slightly different foveal locations on each trial. The data were analyzed assuming a binomial probability for sampling of L and M cones and Poisson distributed quantal fluctuation. Under these assumptions, the measurements imply that detection requires a minimum of 5-7 quanta absorbed per cone, and that the effective number of cones illuminated by the 1', 0.5 msec pulse is two. The estimated L/M cone ratio was 1.6 for one observer and 4.0 for the other; each observer's ratio was in general agreement with the value estimated independently by heterochromatic flicker photometry.

Adult↗

PubMed1987

A central binocular mechanism affects chromatic adaptation.

Two experiments explored the role of central binocular mechanisms in color perception. The first experiment examined the effect of adapting to simultaneous, binocularly fused fields. Each eye adapted to a slowly flickering (0.5 Hz) long-wavelength light. The two eyes were adapted either inphase (both eyes stimulated at the same moment) or out-of-phase (only one eye stimulated at any given moment). Both adapting procedures shifted equilibrium yellow toward longer wavelengths, but a significantly greater shift was found when adapting light stimulated both eyes simultaneously. This reveals that a central binocular mechanism affects chromatic adaptation. The second experiment tested whether the binocular mechanism could shift equilibrium yellow measurements made with both eyes (identical, binocularly fused fields presented to each eye) outside of the range of measurements established by left-eye monocular viewing and right-eye monocular viewing. Differences were found between monocular left-eye and monocular right-eye color appearance under conditions of moderate chromatic adaptation, but binocularly fused measurements fell within the range established by the monocular results. This is consistent with the view that central mechanisms serve to keep the two eyes in balance, rather than systematically alter color appearance from colors perceived under monocular viewing.

Adaptation, Ocular↗

PubMed1987

Appearance of steadily viewed lights.

An interocular matching technique was used to investigate the variation of chromaticity and brightness following steady viewing of a chromatic test light (identical adapting and testing color). Adaptation times were of sufficient duration to ensure stable matches. Following chromatic adaptation we found changes in hue, saturation and brightness. The spectral colors appeared desaturated. The hue shift for the spectral region 546 to 570 nm was towards green and for 586 to 670 nm was towards red. The brightness decrease, independent of chromaticity, was 0.8 log unit at 150 td and 0.3 log unit at 8 td. Data were analyzed within a two-process framework of brightness. Bezold-Brücke effect measurements showed chromaticity shifts in the same direction as for dimming caused by continuous adaptation. Changes in saturation were also observed but were usually in the opposite direction from those found for adaptation.

Adaptation, Ocular↗

PubMed1984

Theoretical interpretation of extraction (in brain) of peptides including concentration variations.

The transport properties of several peptides across blood-brain barrier (BBB) have been investigated theoretically in terms of simple diffusion and facilitated diffusion processes. Comparison of the calculated results from the simple diffusion and the experimental data reveals the presence of the facilitated diffusion of these substances which we have conceived of as a carrier-mediated process. The values of the partition coefficients f for these peptides were in the range 7 X 10(-4) less than or equal to f less than or equal to 200 X 10(-4). The calculated f values gave permeabilities, Ps, in lipids between 10(-7) less than or equal to Ps less than or equal to 14 X 10(-7) cm/s. These values were then used to estimate the extraction for peptides from simple diffusion alone which vary from 0.3 to 3.5% compared with the experimental extraction (0.4-12%) indicating the inadequacy of the simple diffusion alone to explain the experimental data. As for the carrier-mediated facilitated diffusion process we have used the activated-complex theory. The extraction in this case depends on the maximal rate of transport (Tmax)f and the reciprocal of the affinity constant Kt for the transport of peptides through BBB. We have deduced that (Tmax)f approximately 0.46 X 10(-3) pmol/g X s and Kt approximately 0.35 nM for Met-enkephalin (Met-ENK), Leu-enkephalin (Leu-ENK), glutathione, carnosine, alpha-MSH and MIF and (Tmax)f approximately 10 X 10(-3) pmol/g X s and Kt approximately 7 nM for AVP, beta LT, beta E and alpha E to explain the observed results. We have also obtained the quantitative variation of extraction with concentration of peptides in the brain-capillary and have established that the extraction decreases with increasing concentration of peptides, tending to a small constant value at high concentrations. It has been inferred that carrier-mediated facilitated diffusion is important for the transport of peptides across BBB.

Animals↗

PubMed1984

Sleep and purposive behavior: inverse deviations from randomness of neuronal firing patterns in the feline thalamus. A new form of homeostasis?

In behaving cats trained to press a bar for small aliquots of milk reward, single neuronal firing patterns were monitored from the nucleus reticularis (NR) thalami during bar bressing (BP), subsequent quiet wakefulness with EEG spindles (S- QW ), grooming behavior (GR) and slow-wave sleep (SWS). The temporal patterns in the neuronal spike trains were analyzed using a non-parametric method based on relative relations between sequential spike intervals. The deviations of pattern occurrences from the random model were quantified. During BP, specific patterns occurred much more often while others occurred much less often than predicted by the random model. Patterns that were dominant during BP, were selectively suppressed or virtually eliminated during S- QW , GR and SWS, despite the increased firing rate; and, vice versa, patterns that were suppressed below chance level during BP, became dominant during S- QW , GR and SWS. The magnitudes of these inversions of the statistical distribution of patterns were not random but graded and positively correlated, thus indicating that they were homeostatically controlled. Since the inversions were already evident shortly after the satiated ceased bar pressing, they may be related to the 'need' for sleep. On the basis of the known mechanisms of pattern generation and changes in receptors for putative transmitters, it was postulated that the inversions of pattern distribution are related to the recuperative function of SWS, i.e. resensitization of receptors that had been desensitized during the animal's stereotypic BP performance. The NR and other neuronal ensembles seem to constitute an oscillatory system with two modes of reciprocal connectivities : one is supporting wakefulness and emission of specific firing patterns, and the other is incompatible with wakefulness and instead is associated with inversion of statistical distribution of firing patterns and recuperative function of SWS.

Animals↗