A Comparative Study of the Spatial-Frequency Spectrum of Different Letter Optotypes and its Role in Target Recognition

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 214-214 ◽  
Author(s):  
S A Koskin ◽  
V F Danilichev ◽  
Y E Shelepin
Keyword(s):  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Frequency Spectrum ◽  
Brain Diseases ◽  
Sinusoidal Grating ◽  
Sensitivity Functions ◽  
Spatial Frequencies ◽  
Wide Range ◽  
Narrow Frequency Band ◽  
Spatial Frequency Spectrum

We studied the contrast sensitivity functions (CSFs) in patients with different eye and brain diseases using a computerised sinusoidal grating test with a wide range of frequencies (0.4 – 19.0 cycles deg−1), the Pelli - Robson chart and a new chart with frequency-filtered Snellen optotypes. The patients had different CSF curves with a decrease of contrast sensitivity in the low, middle, or high frequencies depending on their main disease (refraction anomalies, cataract, glaucoma, neuritis of optic nerve, brain tumours, etc). Analysis showed that optotypes in the Pelli - Robson chart have a wide-range spatial-frequency spectrum, and optotype recognition is determined not only by low spatial frequencies. We find that the recognition of standard Sloan's optotypes is determined mostly by sensitivity in the range of 9.4 – 14.0 cycles deg−1. At the same time we measured contrast sensitivity using the new filtered Snellen optotypes. Our calculations support our earlier suggestions that the new filtered optotypes have a narrow-band spatial-frequency spectrum, thus enabling selective measurement of contrast sensitivity in each narrow frequency band.

Contrast Sensitivity and Spatial-Frequency Spectrum After Refractive Surgery

2003 ◽  
Vol 29 (9) ◽  
pp. 1650-1651 ◽  
Author(s):  
Robert Montés-Micó ◽  
Jorge L. Alió ◽  
Gonzalo Muñoz
Keyword(s):  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Frequency Spectrum ◽  
Refractive Surgery ◽  
Spatial Frequency Spectrum

Spatial Integration of Objectively Equiluminous Chromatic Gratings

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 200-200
Author(s):  
M I Kankaanpää ◽  
J Rovamo ◽  
H T Kukkonen ◽  
J Hallikainen
Keyword(s):  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Spatial Integration ◽  
Chromatic Contrast ◽  
Shape Difference ◽  
Sensitivity Functions ◽  
Spatial Frequencies ◽  
Low Pass ◽  
Chromatic Aberrations ◽  
Chromatic Contrast Sensitivity

Contrast sensitivity functions for achromatic and chromatic gratings tend to be band-pass and low-pass in shape, respectively. Our aim was to test whether spatial integration contributes to the shape difference found at low spatial frequencies. We measured binocular chromatic contrast sensitivity as a function of grating area for objectively equiluminous red - green and blue - yellow chromatic gratings. Chromatic contrast refers to the Michelson contrast of either of the two chromatic component gratings presented in counterphase against the combined background. Grating area ( A) varied from 1 to 256 square cycles ( Af2) at spatial frequencies ( f) of 0.125 – 4.0 cycles deg−1. We used only horizontal gratings at low and medium spatial frequencies to minimise the transverse and longitudinal chromatic aberrations due to ocular optics. At all spatial frequencies studied, chromatic contrast sensitivity increased with grating area. Ac was found to be constant at low spatial frequencies (0.125 – 0.5 cycles deg−1) but decreased in inverse proportion to increasing spatial frequency at 1 – 4 cycles deg−1. Thus, spatial integration depends similarly on spatial frequency for achromatic (Luntinen et al, 1995 Vision Research35 2339 – 2346) and chromatic gratings, and differences in spatial integration do not contribute to the shape difference of the respective contrast sensitivity functions.

scholarly journals Practical Color Contrast Sensitivity Functions for Luminance Levels up to 10000 cd/m2

2020 ◽  
Vol 2020 (28) ◽  
pp. 1-6
Author(s):  
Rafał K. Mantiuk ◽  
Minjung Kim ◽  
Maliha Ashraf ◽  
Qiang Xu ◽  
M. Ronnier Luo ◽  
...  
Keyword(s):  
Contrast Sensitivity ◽  
Dynamic Range ◽  
Color Space ◽  
High Dynamic Range ◽  
Model Parameters ◽  
Color Contrast ◽  
Sensitivity Functions ◽  
Spatial Frequencies ◽  
Wide Range ◽  
Opponent Color

We model color contrast sensitivity for Gabor patches as a function of spatial frequency, luminance and chromacity of the background, modulation direction in the color space and stimulus size. To fit the model parameters, we combine the data from five independent datasets, which let us make predictions for background luminance levels between 0.0002 cd/m2 and 10 000 cd/m2, and for spatial frequencies between 0.06 cpd and 32 cpd. The data are well-explained by two models: a model that encodes cone contrast and a model that encodes postreceptoral, opponent-color contrast. Our intention is to create practical models, which can well explain the detection performance for natural viewing in a wide range of conditions. As our models are fitted to the data spanning very large range of luminance, they can find applications in modeling visual performance for high dynamic range and augmented reality displays.

Acuity and contrast sensitivity of the bluegill sunfish and how they change during optic nerve regeneration

2007 ◽  
Vol 24 (3) ◽  
pp. 319-331 ◽  
Author(s):  
D.P.M. NORTHMORE ◽  
D.-J. OH ◽  
M.A. CELENZA
Keyword(s):  
Optic Nerve ◽  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Cutoff Frequency ◽  
Lepomis Macrochirus ◽  
High Spatial Frequency ◽  
Contrast Threshold ◽  
Bluegill Sunfish ◽  
Sensitivity Functions ◽  
Spatial Frequencies

Spatial vision was studied in the bluegill sunfish, Lepomis macrochirus (9.5–14 cm standard length) to assess the limitations imposed by the optics of the eye, the retinal receptor spacing and the retinotectal projection during regeneration. Examination of images formed by the dioptric elements of the eye showed that spatial frequencies up to 29 c/° could be imaged on the retina. Cone spacing was measured in the retina of fresh, intact eyes. The spacing of rows of double cones predicted 3.4 c/° as the cutoff spatial frequency; the spacing between rows of single and double cones predicted 6.7 c/°. Contrast sensitivity functions were obtained psychophysically in normals and fish with one regenerating optic nerve. Fish were trained to orient to gratings (mean luminance = 25 cd/m2) presented to either eye. In normals, contrast sensitivity functions were similar in shape and bandwidth to those of other species, peaking at 0.4 c/° with a minimum contrast threshold of 0.03 and a cutoff at about 5 c/°, which was within the range predicted by cone spacing. Given that the optical cutoff frequency exceeds that predicted by cone spacing, it is possible that gratings could be detected by aliasing with the bluegill's regular cone mosaic. However, tests with high contrast gratings up to 15 c/° found no evidence of such detection. After crushing one optic nerve in three trained sunfish, recovery of visual avoidance, dorsal light reflex and orienting to gratings, were monitored over 315 days. At 64–69 days postcrush, responses to gratings reappeared, and within 2–5 days contrast sensitivity at low (0.15 c/°) and medium (1.0 c/°) spatial frequencies had returned to normal. At a high spatial frequency (2.93 c/°) recovery was much slower, and complete only in one fish.

scholarly journals Sharpening coarse-to-fine stereo vision by perceptual learning: asymmetric transfer across the spatial frequency spectrum

2016 ◽  
Vol 3 (1) ◽  
pp. 150523 ◽  
Author(s):  
Roger W. Li ◽  
Truyet T. Tran ◽  
Ashley P. Craven ◽  
Tsz-Wing Leung ◽  
Sandy W. Chat ◽  
...  
Keyword(s):  
Spatial Frequency ◽  
Perceptual Learning ◽  
Frequency Spectrum ◽  
Three Dimensional ◽  
High Spatial Frequency ◽  
Visual Image ◽  
Spatial Frequencies ◽  
Early Visual Cortex ◽  
Coarse To Fine ◽  
Spatial Frequency Spectrum

Neurons in the early visual cortex are finely tuned to different low-level visual features, forming a multi-channel system analysing the visual image formed on the retina in a parallel manner. However, little is known about the potential ‘cross-talk’ among these channels. Here, we systematically investigated whether stereoacuity, over a large range of target spatial frequencies, can be enhanced by perceptual learning. Using narrow-band visual stimuli, we found that practice with coarse (low spatial frequency) targets substantially improves performance, and that the improvement spreads from coarse to fine (high spatial frequency) three-dimensional perception, generalizing broadly across untrained spatial frequencies and orientations. Notably, we observed an asymmetric transfer of learning across the spatial frequency spectrum. The bandwidth of transfer was broader when training was at a high spatial frequency than at a low spatial frequency. Stereoacuity training is most beneficial when trained with fine targets. This broad transfer of stereoacuity learning contrasts with the highly specific learning reported for other basic visual functions. We also revealed strategies to boost learning outcomes ‘beyond-the-plateau’. Our investigations contribute to understanding the functional properties of the network subserving stereovision. The ability to generalize may provide a key principle for restoring impaired binocular vision in clinical situations.

scholarly journals Are Contrast Sensitivity Functions Impaired in Insulin Dependent Diabetics Without Diabetic Retinopathy?

1999 ◽  
Vol 42 (4) ◽  
pp. 133-138 ◽  
Author(s):  
Vladimír Liška ◽  
Miroslav Dostálek
Keyword(s):  
Visual Acuity ◽  
Diabetic Retinopathy ◽  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Dependent Diabetes Mellitus ◽  
Control Group ◽  
Study Group ◽  
Sensitivity Functions ◽  
Spatial Frequencies ◽  
Insulin Dependent

Purpose: To confirm the influence of multilevel metabolic disturbance of insulin dependent diabetes mellitus (IDDM) on the vision even before the onset of the other changes routinely evaluated by ophthalmologists. Methods: Contrast sensitivity functions (CSFs) were estimated using the VCTS 6500 board. The standardised measurement procedure was performed. The value of the threshold contrast sensitivity was obtained for five spatial frequencies (1.5 - 3 - 6 - 12 - 18 c/deg). Other data was collected (duration of diabetes, BCVA, funduscopy, fluoresceine angiography, HbA1C). The study group consisted of 48 IDDM patients (94 eyes) without diabetic retinopathy and with Snellen BCVA > 1.0. The control group (56 normals, 98 eyes) was age and BCVA matched. Results: Highly statistically significant decrease of the CSFs in all spatial frequencies in the study group was obtained. Correlation between duration of the diabetes and impaired degree of CSFs was present in the middle spatial frequency. No significant changes in CSFs were found among patients with pathological value of glycated hemoglobin HbA1c (>7.8 %). Conclusions: If compared with routinely used Snellen visual acuity, the CSFs are more complex descriptors of the subjects vision abilities. IDDM has an influence on these sensitive functions, especially during examination in the middle spatial frequency of 6 and 12 c/deg, before disturbing visual acuity and before changes in the retinal morphology. Decrease of CSFs was influenced mainly by the patients’ age and partially (in the middle spatial frequency) by the IDDM duration.

Extrageniculostriate vision in the monkey. VII. Contrast sensitivity functions

1980 ◽  
Vol 43 (6) ◽  
pp. 1510-1526 ◽  
Author(s):  
M. Miller ◽  
P. Pasik ◽  
T. Pasik
Keyword(s):  
Spatial Frequency ◽  
Contrast Sensitivity ◽  
Striate Cortex ◽  
Pattern Discrimination ◽  
Sensitivity Threshold ◽  
Sinusoidal Grating ◽  
Frequency Detection ◽  
Spatial Frequencies ◽  
The Mean ◽  
Method Of Constant Stimuli

1. Psychophysical and electrophysiological experiments have indicated the importance of spatial frequency components and their respective contrasts and orientations for the recognition of patterns. It is in the striate cortex where these types of information first converge, a fact that lends support to the accepted crucial role of this structure in pattern discrimination. 2. Monkeys with total bilateral ablation of the striate cortex, however, retain a residual capacity for pattern discrimination and also can differentiate between a vertical and an oblique luminous bar. The present study explores their capacity for spatial frequency detection both as a function of contrast and, by extrapolation, at maximum contrast (visual acuity measure). 3. Monkeys were presented with a forced choice between a homogeneous target and a vertically oriented sinusoidal grating in a pulling-in apparatus. Stimuli were produced by the transillumination of transparencies at spatial frequencies of 0.5, 1.0, 2.0, 4.0, 8.0, 16, and 32 cycles/deg, in 0.1-log unit steps of contrast from 0.79 to 0.006. The stimuli subtended 8 degrees of visual angle and were matched for mean luminance at 20 cd/m2. After mastering the discrimination of one spatial frequency at the highest contrast, contrast thresholds were first estimated by a staircase technique, and then determined by the method of constant stimuli. The procedure was repeated for each spatial frequency before and after histologically verified total bilateral removal of striate cortex and partial damage to circumstriate cortices. 4. Discrimination at all spatial frequencies was mastered by all normal monkeys. Postoperatively, they could solve only problems with frequencies between 0.5 and 4.0 cycles/deg. 5. Contrast sensitivity (threshold-1) functions for normal and destriated monkeys have the characteristic inverted J shape. The high- and low-frequency limbs are related exponentially to spatial frequency, and the peak of the curve is about 2.0 cycles/deg. The dimensions of the functions, however, change significantly following the ablation. Sensitivity is depressed at all spatial frequencies. The mean “visuogram” indicates a 26-dB flat loss. 6. The mean high-frequency cutoff point is 43 cycle/deg preoperatively and 12 cycles/deg postoperatively, equivalent to 0.7' and 2.5' of arc, respectively. The latter value is not worse than 20/80 on the Snellen chart. 7. The variability of the response at each spatial frequency in the staircase method and the slope of the psychometric function derived from the method of constant stimuli provide a measure of “instability” and “precision,” respectively, which are inversely related. Preoperatively, precision is significantly greater at high than at low spatial frequencies. Postoperatively, it is similar at all frequencies, and the values are lower than those determined preoperatively. 8. The results demonstrate that destriated monkeys can detect gratings, although to a lesser degree than normal animals…

Spatial-frequency and orientation tuning in psychophysical end-stopping

1998 ◽  
Vol 15 (4) ◽  
pp. 585-595 ◽  
Author(s):  
CONG YU ◽  
DENNIS M. LEVI
Keyword(s):  
Spatial Frequency ◽  
Frequency Tuning ◽  
Spatial Filter ◽  
Orientation Tuning ◽  
Maximal Strength ◽  
Facilitation Effect ◽  
Spatial Filters ◽  
Spatial Frequency Tuning ◽  
Spatial Frequencies ◽  
Wide Range

A psychophysical analog to cortical receptive-field end-stopping has been demonstrated previously in spatial filters tuned to a wide range of spatial frequencies (Yu & Levi, 1997a). The current study investigated tuning characteristics in psychophysical spatial filter end-stopping. When a D6 (the sixth derivative of a Gaussian) target is masked by a center mask (placed in the putative spatial filter center), two end-zone masks (placed in the filter end-zones) reduce thresholds. This “end-stopping” effect (the reduction of masking induced by end-zone masks) was measured at various spatial frequencies and orientations of end-zone masks. End-stopping reached its maximal strength when the spatial frequency and/or orientation of the end-zone masks matched the spatial frequency and/or orientation of the target and center mask, showing spatial-frequency tuning and orientation tuning. The bandwidths of spatial-frequency and orientation tuning functions decreased with increasing target spatial frequency. At larger orientation differences, however, end-zone masks induced a secondary facilitation effect, which was maximal when the spatial frequency of end-zone masks equated the target spatial frequency. This facilitation effect might be related to certain types of contour and texture perception, such as perceptual pop-out.

Visual Contrast Sensitivity Functions Obtained with Colored and Achromatic Gratings

1979 ◽  
Vol 21 (2) ◽  
pp. 225-228 ◽  
Author(s):  
Michael A. Nelson ◽  
Ronald L. Halberg
Keyword(s):  
Contrast Sensitivity ◽  
Spatial Information ◽  
Sensitivity Functions ◽  
Visual Contrast ◽  
Spatial Frequencies ◽  
Sinusoidal Gratings ◽  
Visual Contrast Sensitivity ◽  
Contrast Thresholds

Threshold contrasts for red, green, and achromatic sinusoidal gratings were measured. Spatial frequencies ranged from 0.25 to 15 cycles/deg. No significant differences in contrast thresholds were found among the three grating types. From this finding it was concluded that, under conditions of normal viewing, no significant differences should be expected in the acquisition of spatial information from monochromatic or achromatic displays of equal resolution.

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