Colour Pools, Brightness Pools, Assimilation, and the Spatial Resolving Power of the Human Colour-Vision System

Perception ◽  
1993 ◽  
Vol 22 (3) ◽  
pp. 343-351 ◽  
Author(s):  
Bernard Moulden ◽  
Fred Kingdom ◽  
Brian Wink
Keyword(s):  
Colour Vision ◽  
Vision System ◽  
Spatial Scales ◽  
Receptive Fields ◽  
Luminance Contrast ◽  
Resolving Power ◽  
Spatial Pooling ◽  
Infant Vision ◽  
Spatial Frequencies ◽  
Normal Colour

A stimulus is described that demonstrates the spatial pooling of colour information in the visual system. Chequerboards (or gratings) consisting of alternating squares (or stripes) of complementary colours become achromatic at particular spatial scales; such stimuli have been named ‘transchromatic’ stimuli. Colour pools are much larger than the receptive fields that respond to luminance contrast. Some measurements are described which form the basis for estimates of the size of the colour pools. The size of colour pools varies according to the colours involved. For red—cyan and green—magenta complementary pairs colour is pooled at spatial frequencies above about 7–8 cycles deg−1, implying pools whose diameter is around 8 min arc. For yellow—blue complementary pairs the corresponding figures are about 4 cycles deg−1 and 15 min arc. Some phenomena of normal colour vision, colour blindness, and the development of infant vision are discussed in the light of these findings.

The response dynamics of primate visual cortical neurons to simulated optical blur

2009 ◽  
Vol 26 (4) ◽  
pp. 411-420 ◽  
Author(s):  
MICHAEL L. RISNER ◽  
TIMOTHY J. GAWNE
Keyword(s):  
Cortical Neurons ◽  
Receptive Fields ◽  
Luminance Contrast ◽  
Form Perception ◽  
Response Dynamics ◽  
V1 Neurons ◽  
Spatial Frequencies ◽  
Wide Range ◽  
Optical Blur ◽  
Visual Cortical

AbstractNeurons in visual cortical area V1 typically respond well to lines or edges of specific orientations. There have been many studies investigating how the responses of these neurons to an oriented edge are affected by changes in luminance contrast. However, in natural images, edges vary not only in contrast but also in the degree of blur, both because of changes in focus and also because shadows are not sharp. The effect of blur on the response dynamics of visual cortical neurons has not been explored. We presented luminance-defined single edges in the receptive fields of parafoveal (1–6 deg eccentric) V1 neurons of two macaque monkeys trained to fixate a spot of light. We varied the width of the blurred region of the edge stimuli up to 0.36 deg of visual angle. Even though the neurons responded robustly to stimuli that only contained high spatial frequencies and 0.36 deg is much larger than the limits of acuity at this eccentricity, changing the degree of blur had minimal effect on the responses of these neurons to the edge. Primates need to measure blur at the fovea to evaluate image quality and control accommodation, but this might only involve a specialist subpopulation of neurons. If visual cortical neurons in general responded differently to sharp and blurred stimuli, then this could provide a cue for form perception, for example, by helping to disambiguate the luminance edges created by real objects from those created by shadows. On the other hand, it might be important to avoid the distraction of changing blur as objects move in and out of the plane of fixation. Our results support the latter hypothesis: the responses of parafoveal V1 neurons are largely unaffected by changes in blur over a wide range.

Cooperative Representation of Visual Borders

Perception ◽  
1992 ◽  
Vol 21 (2) ◽  
pp. 185-193 ◽  
Author(s):  
Geoffrey W Stuart ◽  
Terence R J Bossomaier
Keyword(s):  
Spatial Frequency ◽  
Spatial Scales ◽  
Receptive Fields ◽  
Frequency Content ◽  
Cortical Cells ◽  
Firing Rates ◽  
Spatial Frequencies ◽  
Cooperative Coding ◽  
Stimulus Features ◽  
Visual Cortical

Recently it has been reported that the visual cortical cells which are engaged in cooperative coding of global stimulus features, display synchrony in their firing rates when both are stimulated. Alternative models identify global stimulus features with the coarse spatial scales of the image. Versions of the Munsterberg or Café Wall illusions which differ in their low spatial frequency content were used to show that in all cases it was the high spatial frequencies in the image which determined the strength and direction of these illusions. Since cells responsive to high spatial frequencies have small receptive fields, cooperative coding must be involved in the representation of long borders in the image.

scholarly journals Neural mechanisms mediating responses to abutting gratings: Luminance edgesvs.illusory contours

2006 ◽  
Vol 23 (2) ◽  
pp. 181-199 ◽  
Author(s):  
YUNING SONG ◽  
CURTIS L. BAKER
Keyword(s):  
Spatial Scales ◽  
Receptive Fields ◽  
Low Frequency ◽  
Neuronal Responses ◽  
Motion Direction ◽  
Frequency Responses ◽  
Energy Mechanism ◽  
Nonlinear Responses ◽  
Spatial Frequencies ◽  
Visual Mechanism

The discontinuities of phase-shifted abutting line gratings give rise to perception of an “illusory contour” (IC) along the line terminations. Neuronal responses to such ICs have been interpreted as evidence for a specialized visual mechanism, since such responses cannot be predicted from conventional linear receptive fields. However, when the spatial scale of the component gratings (carriers) is large compared to the neuron's luminance passband, these IC responses might be evoked simply by the luminance edges at the line terminations. Thus by presenting abutting gratings at a series of carrier spatial scales to cat A18 neurons, we were able to distinguish genuine nonlinear responses from those due to luminance edges. Around half of the neurons (both simple and complex types) showed a bimodal response pattern to abutting gratings: one peak at a low carrier spatial frequency range that overlapped with the luminance passband, and a second distinct peak at much higher frequencies beyond the neuron's grating resolution. For those bimodally responding neurons, the low-frequency responses were sensitive to carrier phase, but the high-frequency responses were phase-invariant. Thus the responses at low carrier spatial frequencies could be understoodviaa linear model, while the higher frequency responses represented genuine nonlinear IC processing. IC responsive neurons also demonstrated somewhat lower spatial preference to the periodic contours (envelopes) compared to gratings, but the optimal orientation and motion direction for both were quite similar. The nonlinear responses to ICs could be explained by the same energy mechanism underlying responses to second-order stimuli such as contrast-modulated gratings. Similar neuronal preferences for ICs and for gratings may contribute to the form-cue invariant perception of moving contours.

Responses to sinusoidal gratings of two types of very nonlinear retinal ganglion cells of cat

1989 ◽  
Vol 3 (3) ◽  
pp. 213-223 ◽  
Author(s):  
J. B. Troy ◽  
G. Einstein ◽  
R. P. Schuurmans ◽  
J. G. Robson ◽  
Ch. Enroth-Cugell
Keyword(s):  
Spatial Frequency ◽  
Ganglion Cells ◽  
Cell Model ◽  
Second Harmonic ◽  
Temporal Frequency ◽  
Receptive Fields ◽  
Cell Types ◽  
Luminance Contrast ◽  
Spatial Frequencies ◽  
Low Pass

AbstractPerhaps 35% of all of the ganglion cells of the cat do not have classical center-surround organized receptive fields. This paper describes, quantitatively, the responses of two such cell types to stimulation with sinusoidal luminance gratings, whose spatial frequency, mean luminance, contrast, and temporal frequency were varied independently. The patterns were well-focused on the retina of the anesthetized and paralyzed cat. In one type of cell, the maintained discharge was depressed or completely suppressed when a contrast pattern was imaged onto the receptive field (suppressed-by-contrast cell). In the other type of cell, the introduction of a pattern elicited a burst of spikes (impressed-by-contrast cell).When stimulated with drifting gratings, the cell's mean rate of discharge was reduced (suppressed-by-contrast cell) or elevated (impressed-by-contrast cell) over a limited band of spatial frequencies. There was no significant modulated component of response. The reduction in mean rate of suppressed-by-contrast cells caused by drifting gratings had a monotonic dependence on contrast, a relatively low-pass temporal-frequency characteristic and was greater under photopic than mesopic illuminance. If gratings of spatial frequency, that when drifted evoked a response from these cells, were instead held stationary and contrast-reversed, the mean rate of a suppressed-by-contrast cell was also reduced and that of an impressed-by-contrast cell increased. But, for contrast-reversed gratings, the discharge contained substantial modulation at even harmonic frequencies, the largest being the second harmonic. The amplitude of this second harmonic did not depend on the spatial phase of the grating, and its dependence on spatial frequency, at least for suppressed-by-contrast cells, was similar to that of the reduction in mean rate of discharge. Our results suggest that the receptive fields of suppressed-by-contrast and impressed-by-contrast cells can be modeled with the general form of the nonlinear subunit components of Hochstein and Shapley's (1976) Y cell model.

Modelling the effects of inter-observer variation on colour rendition

2017 ◽  
Vol 51 (1) ◽  
pp. 37-54 ◽  
Author(s):  
MJ Murdoch ◽  
MD Fairchild
Keyword(s):  
Colour Vision ◽  
Spectral Characteristics ◽  
Observer Variation ◽  
Light Sources ◽  
Standard Observer ◽  
Natural Range ◽  
Normal Colour ◽  
Range Of Variation

The colour rendition characteristics of light sources are quantified with measures based on CIE standard observers, which are reasonable representations of population averages. However, even among people with normal colour vision, the natural range of variation in colour sensitivity means any individual may see something different than the standard observer. Modelling results quantify the effects of these inter-observer differences on colour rendition measures defined by IES TM-30-15. In general, inter-observer differences tend to be smaller for light sources with high colour fidelity values, and they are affected by spectral characteristics of different lighting technologies. The magnitude of variation in colour rendition measures, up to 5–10 units in IES TM-30-15 ( Rf, Rg), measures is compared with other sources of variability and ambiguity.

Use of Face Information Varies Systematically From Developmental Prosopagnosics to Super-Recognizers

2018 ◽  
Vol 30 (2) ◽  
pp. 300-308 ◽  
Author(s):  
Jessica Tardif ◽  
Xavier Morin Duchesne ◽  
Sarah Cohan ◽  
Jessica Royer ◽  
Caroline Blais ◽  
...  
Keyword(s):  
Face Recognition ◽  
Spatial Scales ◽  
Face Identification ◽  
Facial Features ◽  
Strongly Correlated ◽  
Identification Task ◽  
Spatial Frequencies ◽  
Recognition Ability ◽  
Neurologically Typical

Face-recognition abilities differ largely in the neurologically typical population. We examined how the use of information varies with face-recognition ability from developmental prosopagnosics to super-recognizers. Specifically, we investigated the use of facial features at different spatial scales in 112 individuals, including 5 developmental prosopagnosics and 8 super-recognizers, during an online famous-face-identification task using the bubbles method. We discovered that viewing of the eyes and mouth to identify faces at relatively high spatial frequencies is strongly correlated with face-recognition ability, evaluated from two independent measures. We also showed that the abilities of developmental prosopagnosics and super-recognizers are explained by a model that predicts face-recognition ability from the use of information built solely from participants with intermediate face-recognition abilities ( n = 99). This supports the hypothesis that the use of information varies quantitatively from developmental prosopagnosics to super-recognizers as a function of face-recognition ability.

Effects of strabismus on responsivity, spatial resolution, and contrast sensitivity of cat lateral geniculate neurons

1984 ◽  
Vol 52 (3) ◽  
pp. 538-552 ◽  
Author(s):  
K. R. Jones ◽  
R. E. Kalil ◽  
P. D. Spear
Keyword(s):  
Contrast Sensitivity ◽  
Spatial Resolution ◽  
Striate Cortex ◽  
Receptive Fields ◽  
Orienting Response ◽  
Lateral Geniculate ◽  
Spatial Frequencies ◽  
Area Centralis ◽  
X Cells ◽  
Y Cells

Rearing cats with esotropia is known to cause a number of deficits in visual behavior tested through the deviated eye. These include a loss of orienting response to stimuli presented in the nasal visual field of the deviated eye, a reduction in visual acuity, and a general reduction in contrast sensitivity at all spatial frequencies. To assess the involvement of the lateral geniculate nucleus (LGN) in these deficits, we measured the following: 1) the visual responsiveness of lamina A1 cells with peripheral (more than 10 degrees from area centralis) receptive fields in three esotropic and three normal cats and 2) the spatial resolution and contrast sensitivity of lamina A X-cells with central (within 5 degrees of the area centralis) receptive fields in six esotropic and six normal cats. For comparison, we also measured LGN X-cell spatial resolutions in four exotropic cats and in two cats raised with an esotropia in one eye and the lids of the other eye sutured shut (MD-estropes). Recordings from the lateral portion of lamina A1 in esotropic cats yielded similar numbers of visually responsive cells with far nasal receptive fields as were seen in normal animals. Peak and mean response rates to a flashing spot also were normal. In addition, no differences were found between esotropes and normals in the percentages of X- and Y-cells encountered. These results suggest that the loss of orienting response to stimuli presented in the nasal field (12, 20) is not due to a loss of neural responses in the LGN of esotropic cats. In addition, they suggest that decreases in cell size in lamina A1 of esotropic cats (13, 36; R. E. Kalil, unpublished observations) are not accompanied by marked functional abnormalities of the cells and that cortical abnormalities ipsilateral to the deviated eye (22) are likely to have their origin within striate cortex itself. Recordings from lamina A cells with receptive fields near area centralis revealed that the average X-cell spatial resolution in esotropes (2.1 cycles/deg) was significantly lower than that in normal cats (3.1 cycles/deg). This reduction was seen in all esotropic cats tested and was due both to an increase in the proportion of X-cells with very low spatial resolution and to a loss of X-cells responding to high spatial frequencies (greater than 3.25 cycles/deg). The average spatial resolution of X-cells driven by the deviated eye in MD-esotropes fell midway between those of esotropes and normals. In exotropes, mean X-cell spatial resolution was normal.(ABSTRACT TRUNCATED AT 400 WORDS)

Diurnal changes in retinula cell sensitivities and receptive fields (two-dimensional angular sensitivity functions) in the apposition eyes of Ligia exotica (Crustacea, Isopoda)

2001 ◽  
Vol 204 (2) ◽  
pp. 239-248 ◽  
Author(s):  
T. Hariyama ◽  
V.B. Meyer-Rochow ◽  
T. Kawauchi ◽  
Y. Takaku ◽  
Y. Tsukahara
Keyword(s):  
Receptive Fields ◽  
Resolving Power ◽  
Pigment Cells ◽  
Diurnal Changes ◽  
Two Dimensional ◽  
Angular Sensitivity ◽  
Pigment Granules ◽  
Screening Pigment ◽  
The Difference ◽  
Night And Day

The structural organization of the retinula cells in the eye of Ligia exotica changes diurnally. At night, the microvilli elongate, losing the regular and parallel alignment characteristic of the day condition. Crystalline cones and distal rhabdom tips are not pushed into each other during the day, but at night the rhabdoms protrude into the crystalline cones by up to 5 microm. Screening pigment granules in the retinula cells disperse during the night, but migrate radially towards the vicinity of the rhabdom during the day. No such displacements of the pigment granules of either distal or proximal screening pigment cells were observed. The sensitivity of the eye, monitored by electroretinogram (ERG) recordings, changes diurnally: values at midnight are, on average, 10 times those occurring during the day. However, intracellular recordings from single retinula cells (50 during the day and 50 at night) indicate that the difference between night and day sensitivities is only 2.5-fold. Two-dimensional angular sensitivity curves, indicative of a single unit's spatial sensitivity, had considerably less regular outlines at night than during the day. If based on the 50 % sensitivity level, day and night eyes possessed receptive fields of almost identical width (approximately 2 degrees), but if sensitivities below the 50 % limit were included, then receptive fields at night were significantly more extensive. We suggest that the morphological adaptations and diurnal changes in chromophore content seen in the apposition eye of L. exotica allow this animal to improve its photon capture at night while preserving at least some of the spatial resolving power characteristic of the light-adapted state. This would explain why this animal is capable of performing complex escape behaviours in the presence of predators both in bright and in very dim light.

A Hospital-Based Cross-Sectional Study to Estimate the Prevalence and Sex Distribution of Colour Vision Deficiency among School Going Children Attending a Tertiary Eye Care Center in Kolkata City, West Bengal, India

2021 ◽  
Vol 8 (32) ◽  
pp. 2962-2967
Author(s):  
Rinki Saha ◽  
Indrajit Sarkar ◽  
Tamojit Chatterjee ◽  
Sandip Samaddar ◽  
Suman Chandra Sen
Keyword(s):  
School Children ◽  
Colour Vision ◽  
Care Center ◽  
Cross Sectional Study ◽  
Sex Distribution ◽  
Cross Sectional ◽  
Colour Vision Deficiency ◽  
Cone Pigments ◽  
Normal Colour ◽  
Colour Blindness

BACKGROUND Colour vision is a function of three types of cone pigments present in the retina. Colour vision deficiency is an important disorder of vision that may pose a handicap to the performance of an affected individual. The prevalence of colour blindness varies in different geographical areas. The identification and estimation of the prevalence of colour vision deficiency in school-going children will help to educate and guide the caregivers to help the children in selecting their profession. This study was done to estimate the prevalence, sex distribution, and types of colour vision deficiency among school-going children of 5 to 15 years. METHODS A cross-sectional observational study was done among 500 students to evaluate the colour vision during the period from 1st January 2018 to 30th June 2019 at the Regional Institute of Ophthalmology, Kolkata. Ishihara’s pseudo isochromatic colour vision chart 38th edition was used to assess the school children for colour vision status. The children who were found to be colour blind were further classified into degree and types of colour vision deficiency. RESULTS A total of 500 students (250 male & 250 female) of surrounding schools, in the age group of 5 years to 15 years, were screened. 480 students (96 %) had normal colour vision while 20 (4 %) students were found to have defective colour vision. Prevalence (4 %) for colour blindness was found to be higher in males (3.6 %) than females (0.4 %). It was observed that out of 20 (4 %) colour-blind subjects 3.6 % were protanopes and 0.4 % were deuteranopes. CONCLUSIONS The present study shows the prevalence of colour blindness found to be quite low (4 %) and more common in males (3.6 %) in comparison to females (0.4 %). Protanomaly (3.6 %) was more common than deuteranomaly (0.4 %). KEYWORDS Colour Blindness, Protanomaly, Deuteranomaly, School Children

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