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J Rovamo

Publications and source records attributed to J Rovamo.

17 recordsLinked to original sources
PubMed1992

The effects of colour adaptation and stimulus size on white perception as a function of eccentricity in man.

We studied how much desaturating complementary colour had to be added to blue, green or red after homochromatic adaptation of short duration in order to perceive white or grey at eccentricities of 0-15 deg in the nasal visual field. The CIE 1931 (x,y) chromaticity coordinates corresponding to achromatic perception were subtracted from the chromaticity coordinates of blue, green and red in order to obtain the threshold differences (dx, dy) in chromaticity coordinates. When the stimulus size was constant at all visual field locations, the absolute values of dx and dy decreased with increasing eccentricity, which means that the desaturation threshold for white or grey perception was higher at the fovea than in the periphery. However, when the stimulus size was M-scaled magnifying its size with increasing eccentricity in inverse proportion to the lowest local sampling density of the human retina (cones and ganglion cells at eccentricities 0-10 and above 10 deg, respectively), dx and dy with blue became independent of visual field location except for the very centre of the fovea. However, M-scaling was unsuccessful with green and red. Although M-scaling with green reduced the change in dx and dy as a function of eccentricity, it had no effect on dx and dy with red colour.

Adaptation, Ocular↗
PubMed1992

The influence of eccentricity on position and movement acuities as revealed by spatial scaling.

The rate of decline with increasing eccentricity of several position and movement acuities was measured using a method of spatial scaling. In this method all stimuli at each visual field location are simply magnified versions of each other. The influence of separation and eccentricity were dissociated by presenting stimuli on an iso-eccentric arc. For each task, the rate of decline in performance was quantified by the parameter E2 which represents the eccentricity at which stimulus size must double in order to maintain performance equivalent to that at the fovea. All tasks were found to obey the concept of spatial scaling in that performance at a given field location could be equated with performance at any other location simply by a change of scale. However, the rate at which performance deteriorated with eccentricity varied over an enormous range (over 100-fold) depending on the task itself. The advantage of such diverse peripheral gradients is clear; the goal is to establish the physiological mechanisms which underlie this phenomenon.

Discrimination, Psychological↗
PubMed1992

Contrast sensitivity as a function of spatial frequency, viewing distance and eccentricity with and without spatial noise.

Using computer graphics and a two-alternative forced-choice method we measured threshold contrast as a function of viewing distance, spatial frequency, and eccentricity for gratings with and without added, white two-dimensional spatial noise. Our experiments showed that in spatial noise contrast sensitivity was independent of viewing distance as long as contrast sensitivity was lower with noise than without. With increasing spatial frequency (f) the grating area (A) was reduced in order to keep the relative grating size (Af2) constant. At all spatial frequencies the test gratings thus had the same amount of detail and contour. Noise spectral density was reduced in direct proportion to grating area in order to keep the physical signal-to-noise ratio constant. An increase in spatial frequency was thus accompanied with reductions in grating area and noise spectral density similar to those produced by a corresponding increase in viewing distance. In agreement, contrast detection in spatial noise was found to be independent of spatial frequency as long as contrast sensitivity was lower with noise than without. The effect of increasing eccentricity on visual performance can be compensated for by reducing the viewing distance (M-scaling). Hence, without M-scaling the effect of increasing eccentricity is similar to that of increasing viewing distance. In agreement, we found that contrast sensitivity in spatial noise was independent of eccentricity as long as contrast sensitivity was lower with noise than without.

Adult↗
PubMed1992

Spatial scaling of vernier acuity tasks.

Vernier acuity thresholds for two abutting lines and for a two-dot stimulus were measured as a function of stimulus magnification at eccentricities of 0, 5, 10 and 15 deg using a spatial scaling technique in which all stimuli are simply magnified versions of each other. The advantage of such a technique is that no prior knowledge of a suitable magnification factor with which to increase the size of peripheral stimuli is required. Thresholds for the line stimulus could be successfully scaled by the application of a magnification factor with an E2 value of 1.23-1.78 deg. Further, provided that the effects of dot separation and eccentricity were dissociated, spatial scaling with an E2 value of 1.06-1.96 deg was also successful in removing eccentricity dependence for two-dot vernier thresholds.

Fovea Centralis↗
PubMed1991

Detection of chromatic deviations from white across the human visual field.

We studied how much blue, green, or red light had to be added to or subtracted from white to obtain veridical hue perception (blue, green, red, or their complementary colours) at various locations in the temporal visual field. The CIE 1931 (x, y) chromaticity coordinates corresponding to a veridical hue perception were subtracted from the chromaticity coordinates of the white (0.35, 0.35) in order to obtain the threshold differences (dx, dy) in chromaticity coordinates. When stimulus size was constant at all visual field locations, dx and dy changed with eccentricity. However, when the stimulus was M-scaled by magnifying its size with increasing eccentricity in inverse proportion to the lowest local sampling density across the human retina (cones and ganglion cells at eccentricities 0-10 and above 10 deg, respectively), dx and dy remained constant at all eccentricities.

Adult↗
PubMed1991

Critical flicker frequency to red targets as a function of luminance and flux across the human visual field.

When the number of cells (cones at eccentricities 0-10 deg and ganglion cells above 10 deg) stimulated at various retinal locations was kept constant by enlarging the stimulus area with increasing eccentricity in the temporal visual field (M-scaling), CFF to red stimuli with dark surround increased as a single function of photopic luminous flux, collected by ganglion-cell receptive-field centres and calculated by multiplying Ricco's area with retinal illuminance at each eccentricity studied. The increase of CFF with the logarithm of photopic flux could be best explained by the Collins logarithmic law, the Kelly square-root law was almost equally good and the Ferry-Porter law was poorest. Adopting the general formulation of Corwin and Dunlap (Vision Research, 27, 2119-2123, 1987) the exponent of CFF is 0, 0.5, and 1 for the Collins, Kelly and Ferry-Porter laws, respectively. The exponent that best explained our results was found to be 0-0.3.

Adult↗
PubMed1990

Cortical acuity and the luminous flux collected by retinal ganglion cells at various eccentricities in human rod and cone vision.

Using areally M-scaled, luminance-modulated orange-red and black-and-white gratings, we measured monocular resolution as a function of luminance at various eccentricities in the temporal visual field. In cone vision the increase of grating acuity with luminance became similar at all eccentricities when (1) acuity values were divided by the human cortical magnification factor to express grating resolution in cortical terms (c mm-1) and (2) retinal illuminance was multiplied by Ricco's area to express luminance in terms of photopic luminous flux. The same MF-scaling procedure also applied to scotopic acuity except that the amount of luminous flux collected by retinal ganglion-cell receptive-fields was in rod vision found to increase with eccentricity faster than photopic Ricco's area.

Adult↗
PubMed1989

Analysis of spatial structure in eccentric vision.

The analysis of spatial structure, ie, the encoding of relative positions between pattern elements, was studied in central and eccentric vision. In a two-alternative forced-choice task the observer had to discriminate between two patterns consisting of short line segments. At each trial the two patterns were flashed for 140 msec and the observer indicated whether the patterns were identical or mirror symmetric. Psychometric functions were measured by changing pattern size at each eccentricity in order to find the threshold size allowing 75% of correct responses. The scaling factor, required for discriminating between mirror symmetric and identical patterns independent of eccentricity, was found to be similar to the size-scaling proposed by Levi et al (Vision Res 25:963, 1985) for vernier acuity tasks.

Differential Threshold↗
PubMed1988

Critical flicker frequency as a function of stimulus area and luminance at various eccentricities in human cone vision: a revision of Granit-Harper and Ferry-Porter laws.

When the photopic luminous flux collected by ganglion cells was kept constant at all retinal locations by reducing average stimulus luminance in inverse proportion to photopic Ricco's area (F-scaling), critical flicker frequency to stimuli of 1.2-88 deg2 in area, presented at various eccentricities along the temporal meridian of the visual field, increased as a single logarithmic function of the number of retinal ganglion cells stimulated. Their number was calculated by multiplying stimulus area by the ganglion cell receptive field density of the human retina. When the number of ganglion cells stimulated was kept constant by enlarging the stimulus area in inverse proportion to the ganglion cell density (M-scaling), the logarithm of CFF to green, yellow, orange and red cone-targets increased as parallel linear functions of logarithmic flux, calculated by multiplying retinal illuminance by photopic Ricco's area.

Adult↗
PubMed1987

Retinal ganglion-cell density and receptive-field size as determinants of photopic flicker sensitivity across the human visual field.

At 1, 10, and 50 Hz, photopic flicker sensitivity to a nonpatterned stimulus of constant area and luminance with a small equiluminous surround tended to decrease when eccentricity increased from 0 to 70 deg. The decrease was steeper for lower flicker frequencies. When the stimulus and surround were M scaled by magnifying them in inverse proportion to retinal ganglion-cell sampling density, flicker sensitivity tended to increase with eccentricity. The increase was steeper for higher flicker frequencies. When the stimulus and surround were F scaled by reducing their average luminance in inverse proportion to Ricco's area, flicker sensitivity again decreased with increasing eccentricity, but now the decrease was steeper for higher flicker frequencies. When the stimulus and surround were MF scaled, flicker sensitivity became independent of eccentricity at all flicker rates tested.

Adult↗
PubMed1987

Texture discrimination at different eccentricities.

Differences in preattentive texture discrimination between central vision and peripheral vision were studied with textures composed of random dots. The subject had to discriminate between two textures whose first-order statistics were kept identical but whose second-order statistics were different. For textures of constant retinal size the discrimination was easy in central vision, but the decrease of visual acuity with increasing eccentricity made the textures unresolvable in peripheral vision. When the textures were scaled by the cortical magnification factor derived from the frequency of retinal ganglion cells so that the calculated neural representations of the textures became similar at different eccentricities, texture discrimination became independent of visual field location. This indicates that preattentive texture discrimination based on differences in second-order statistics of random dots operates similarly in central vision and peripheral vision.

Discrimination, Psychological↗
PubMed1986

Perimetry of critical flicker frequency in human rod and cone vision.

Photopic critical flicker frequency (CFF) to green and yellow-red targets became independent of visual field location when the decrease in the density of retinal ganglion cells and increase in their receptive-field size towards the retinal periphery were compensated for by increasing stimulus area in inverse proportion to the human cortical magnification factor squared (M-scaling) and by reducing stimulus luminance in inverse proportion to Ricco's area (F-scaling). In mesopic and scotopic vision CFF to green targets increased monotonically with eccentricity despite MF-scaling. Instead, CFF to MF-scaled yellow-red targets that predominantly stimulated cones was independent of eccentricity at all luminance levels tested.

Adult↗
PubMed1979

Visual resolution, contrast sensitivity, and the cortical magnification factor.

This study shows that photopic contrast sensitivity and resolution can be predicted by means of simple functions derived by using the cortical magnification factor M as a scale factor of mapping from the visual field into the striate cortex. We measured the minimum contrast required for discriminating the direction of movement or orientation of sinusoidal gratings, or for detecting them in central and peripheral vision. No qualitative differences were found between central and peripheral vision, and almost all quantitative differences observed could be removed by means of a size compensation derived from M. The results indicated specifically that (1) visual patterns can be made equally visible if they are scaled so that their calculated cortical representations become equivalent; (2) contrast sensitivity follows the same power function of the cortical area stimulated by a grating at any eccentricity; (3) area and squared spatial frequency are reciprocally related as determinants of contrast sensitivity; and (4) acuity and resolution are directly proportional to M, and the minimum angle of resolution is directly proportional to M-1. The power law of spatial summation expressed in (2) and (3) suggests the existence of a central integrator that pools the activity of cortical neurons. This summation mechanism makes the number of potentially activated visual cells the most important determinant of visibility and contrast sensitivity. The functional homogeneity of image processing across the visual field observed here agrees with the assumed anatomical and physiological uniformity of the visual cortex.

Brain Mapping↗
PubMed1979

An estimation and application of the human cortical magnification factor.

Comparisons of the published data on the density D of receptive fields of retinal ganglion cells and on the cortical magnification factor M indicated that M2 is directly proportional to D in primates. Therefore, the human M can be estimated for the principal meridians of the visual field from the density-distribution of retinal ganglion cells and from the density of the centralmost cones. Using the previously published empirical data, we estimated the values of the human M and express the values in four simple equations that can be used for finding the value of M for any location of the visual field. The monocular values of M are not radially symmetric. These analytically expressed values of M make it possible to predict contrast sensitivity and resolution for any location of the visual field. We measured contrast sensitivity functions at 25 different locations and found that the functions could be made similar by scaling the retinal dimensions of test gratings by the inverse values of M. Visual acuity and resolution could be predicted accurately for all retinal locations by means of a single constant multiplier of the estimated M. The results indicate that the functional and structural properties of the visual system are very closely and similarly related across the whole retina. Visual acuity, e.g., bears the same optimal relation to the density of sampling executed by retinal ganglion cells at all locations of the visual fields.

Brain Mapping↗
PubMed1978

Receptive field density of retinal ganglion cells and cortical magnification factor in man.

A mathematical relationship is derived between the density or retinal ganglion cell receptive fields and cortical magnification factor. The derivation is based on an assumed constant density of visual fibres entering the striate cortex and on a continuous retinotopic mapping of the visual field thereto. After considering the effect of cortical ocular-dominance columns the human cortical magnification factor along the principal meridians of the visual field is calculated from the empirical estimates of receptive field density of ganglion cells in human retina. The computed estimates of cortical magnification factor agree with experimental data obtained from studies of cortically induced phosphenes, visual migraine hallucinations, and contrast sensitivity functions.

Computers↗