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D C Burr

Publications and source records attributed to D C Burr.

At least 55 records · Page 3Linked to original sources

Evidence for edge and bar detectors in human vision.

The structure of receptive fields of human visual detectors was investigated by studying their phase response. Observers were required to discriminate between pairs of periodic stimuli that differed in phase by 180 degrees (reversed in contrast). The stimuli comprised 256 harmonics, smoothly filtered in amplitude, and congruent in phase at the origin. Reversal discrimination thresholds were measured as a function of the phase of the harmonics. Thresholds were slightly higher for phases around 45 degrees, consistent with the idea that all discriminations were mediated by independent detectors with 0 or 90 degrees phase response (assuming probability summation between them). Discrimination thresholds were also measured with a pedestal stimulus, of phase complementary to that of the test gratings. For discriminations between 0 and 180 degrees (cosine phase), or 90 and 270 degrees (sine phase), the complementary pedestal had little effect, implying independence of detectors in sine and cosine phase. However, for discrimination between 45 and 225 degrees (stimuli containing both sine and cosine components) the complementary pedestal, which also contained both sine and cosine components, facilitated greatly discrimination thresholds. The results suggest that there exist two classes of detectors, one with a Fourier phase spectrum of 0, the other with a Fourier phase spectrum of 90 degrees. This implies that the receptive fields are symmetric, one class having even-symmetry (line-detectors), the other odd-symmetry (edge-detectors).

Differential Threshold↗

Discrimination of spatial phase in central and peripheral vision.

Sensitivity to relative phase was measured for central and peripheral vision using stimuli comprising 256 harmonics, smoothly filtered in amplitude. With these stimuli, peripheral phase sensitivity was much higher than that previously reported with two-harmonic stimuli. Sensitivity did not depend on the average phase of the stimuli, nor on their second-order statistics, irrespective of the spatial frequency of the stimulus or the position in the visual field. After scaling for size, peripheral sensitivity was as high as central sensitivity. The scaling factor required to equate phase sensitivity was the same as that required to equate contrast sensitivity and grating acuity. These results suggest that phase sensitivity decreases with eccentricity at a similar rate as contrast sensitivity and grating acuity, much more slowly than the positional acuities. This is consistent with the suggestion that phase discrimination is mediated by discriminating the amplitude of the response of quasi-linear filters, and does not require mechanisms that evaluate position. It is suggested that previous measurements on peripheral phase sensitivity may reflect positional uncertainty in the periphery, rather than a deficit in phase sensitivity per se.

Differential Threshold↗

The conditions under which Mach bands are visible.

In this paper we challenge the classical explanation of Mach bands--that they result from lateral inhibitory mechanism operating in the visual system--and present an alternative explanation based on a recent local energy model of feature detection (Morrone & Burr, 1988). A series of experiments was conducted to establish the range of parameters under which Mach bands appear on periodic waveforms of the trapezoid family. The model predicts successfully the conditions under which Mach bands appear, and the contrast necessary to see them. Other models, including those based on lateral inhibition and band-pass filtering fail to do so.

Contrast Sensitivity↗

Receptive field properties of human motion detector units inferred from spatial frequency masking.

This study was designed to investigate the spatial frequency selectivity and spatial structure of receptive fields of motion sensitive mechanisms in human vision. Spatial frequency selectivity was inferred from masking measurements, using dynamic test and mask stimuli. For test frequencies between 0.025 and 15.0 c/deg, maximal masking occurred when the mask frequency matched that of the test, suggesting that the test was detected by mechanisms tuned to (or near to) that frequency. For tests below 0.025 c/deg or above 15.0 c/deg, maximal masking occurred at 0.025 and 15.0 c/deg, respectively, suggesting that there exist no mechanisms selective to frequencies outside these limits. A masking model, suitable for interpreting results obtained with drifting test stimuli, was developed and used to calculate spatial frequency selectivity functions from masking data. Assuming small signal linearity, and a constant phase spectrum, the selectivity functions were inverse-Fourier transformed to yield estimates of the extent and structure of receptive fields. Field width was found to vary with test spatial frequency from 5.8 deg at 0.03 c/deg to 0.05 deg at 10.0 c/deg. These estimates were compared with width estimates previously obtained by a summation technique (Anderson & Burr, 1987), and found to be similar over a wide range of spatial frequencies (2.5 log units). Gabor functions provided a reasonable fit to the calculated field profiles at high spatial frequencies (above 1.0 c/deg), but not at low frequencies.

Fourier Analysis↗

Feature detection in human vision: a phase-dependent energy model.

This paper presents a simple and biologically plausible model of how mammalian visual systems could detect and identify features in an image. We suggest that the points in a waveform that have unique perceptual significance as 'lines' and 'edges' are the points where the Fourier components of the waveform come into phase with each other. At these points 'local energy' is maximal. Local energy is defined as the square root of the sum of the squared response of sets of matched filters, of identical amplitude spectrum but differing in phase spectrum by 90 degrees: one filter type has an even-symmetric line-spread function, the other an odd-symmetric line-spread function. For a line the main contribution to the local energy peak is in the output of the even-symmetric filters, whereas for edges it is in the output of the odd-symmetric filters. If both filter types respond at the peak of local energy, both edges and lines are seen, either simultaneously or alternating in time. The model was tested with a series of images, and shown to predict well the position of perceived features and the organization of the images.

Computer Simulation↗

Cross-orientation inhibition in cat is GABA mediated.

Visual evoked potentials (VEPs) were recorded from cat cortex (area 17) before, during and after application of the GABA blocker bicuculline (iontophoretic or topical). The stimuli comprised a test sinusoidal grating, and a mask grating oriented either parallel or orthogonal to the test. Both test and mask alternated in contrast at different temporal frequencies. VEPs were averaged in synchrony with the test contrast reversal, so the mask did not contribute directly to the averaged VEP response. Before application of bicuculline, both parallel and orthogonal masks attenuated the amplitude of VEPs and changed the phase response, but in different ways. Orthogonal masks lowered the slope of the contrast response curve without affecting extrapolated threshold, while parallel masks caused the curve to shift to the right. Orthogonal masks increased the phase advance, while parallel masks eliminated it. During application of bicuculline, neither parallel nor the orthogonal masks attenuated VEP amplitudes. The results suggest that although the mechanisms for the action of parallel and orthogonal masks are clearly distinct, both are mediated by the GABA-ergic inhibitory system. Given this evidence, measurement of VEP contrast response curves may provide a simple non-invasive technique for monitoring visual inhibition in humans.

Administration, Topical↗

Receptive field size of human motion detection units.

Receptive field sizes of motion detector units in the human visual system were determined using a summation technique. Contrast sensitivity was measured for detecting the direction of motion of a drifting (8 Hz) sinewave grating (0.01-30.0 c/deg) multiplied by a stationary Gaussian envelope, for various widths of the Gaussian envelope. For each test spatial frequency, sensitivity increased linearly with aperture width up to a certain limit, and thereafter at a rate consistent with a model incorporating probability summation over space and between channels. The limit of linear summation designates the limit of the receptive field. Results show that the receptive field size varies with spatial frequency, from 2' arc at high spatial frequencies to as large as 7 deg at low frequencies. The change in field size was progressive. The smallest aperture width (delta W) for directional discrimination was also measured. Results show delta W to vary from 0.03 cycles at low spatial frequencies to 0.30 cycles at high frequencies.

Discrimination, Psychological↗

Implications of the Craik-O'Brien illusion for brightness perception.

Measurements are reported for detection thresholds of high and low-pass filtered squarewaves, and for brightness matches of those waveforms. The threshold measurements agree closely with those of Campbell, Howell and Johnstone [J. Physiol., Lond. 284, 193-201 (1978)]: contrasts at which a high-pass squarewave was indistinguishable from an unfiltered squarewave could be well predicted from detection thresholds for an appropriate low-pass squarewave. However, the brightness of high-pass squarewaves (the "Craik-O'Brien illusion") was not related to the threshold measurements. Brightness was virtually constant with spatial frequency, even at spatial frequencies 10 times higher than the region of the low frequency cut. Brightness depended strongly on contrast, being relatively greater at low than at high contrasts. The results can be well accounted for by a recent theory of edge detection, and the existence of parallel channels in vision.

Humans↗

Electrophysiological correlates of positive and negative afterimages.

We report here measurements of visual evoked potential (VEP) activity after induction of afterimages in human observers. Drifting gratings normally produce no measurable phase synchronized VEP. However, after an afterimage of a high contrast grating of the same orientation and spatial frequency of that of the drifting grating has been flashed on the retina. VEPs in synchrony with the drift frequency are produced. For up to about two minutes after the flash, the VEPs were all clustered in one phase, then declined for a minute or so, to reappear 180 degrees out of phase from the first VEPs. The first group of VEPs coincides with the percept of a positive afterimage, and the second with that of a negative afterimage. Possible explanations for the existence of positive and negative afterimages and the associated VEPs are considered.

Afterimage↗

Inhibitory interactions in the human vision system revealed in pattern-evoked potentials.

1. Visual evoked potentials (v.e.p.s) were recorded from human adults to investigate orientation-specific neural interactions. The stimuli were the sum of two gratings, sinusoidally modulated in space and time at different frequencies. Recordings were made for one grating (test) alone, and with another superimposed grating (mask), oriented parallel or orthogonal to the test. The amplitude and phase of the v.e.p.s at twice the test modulation frequency (second harmonic) was measured as a function of test contrast to produce contrast-response curves. 2. Orthogonal masks attenuated considerably the amplitude of v.e.p.s. The attenuation at any given contrast was approximately proportional, or multiplicative, lowering the slope of the contrast-response curve, without affecting significantly the extrapolated threshold. Parallel masks also attenuated v.e.p. amplitudes but in a different way, leaving the slope of the contrast-response curves unchanged, while elevating threshold. 3. The attenuation by orthogonal masks occurred over a wide range of test spatial frequencies, from 0.8 to 8 cycles/deg. For any given test spatial frequency, the most effective masks were those of spatial frequency similar to or lower than the test. Masks of spatial frequency 1.5 octaves higher than the test did not attenuate v.e.p. amplitudes. 4. The mask temporal frequency for maximal attenuation of v.e.p. amplitude was around 12 Hz, with stationary masks having little effect. 5. Under most conditions, the phase of the second harmonic of the v.e.p., increased with increasing contrast (phase advance). Superimposition of a parallel mask abolished phase advance, while orthogonal masks increased it. 6. Comparisons with single cortical unit and evoked potential recordings in cats suggest that the attenuation by orthogonal masks reflects intracortical inhibitory interactions between cell populations of different orientation preference.

Adult↗

Seeing objects in motion.

This paper reports estimates of the conjoint spatiotemporal tuning functions of the neural mechanisms of the human vision system which detect image motion. The functions were derived from measurements of the minimum contrast necessary to detect the direction of drift of a sinusoidal grating, in the presence of phase-reversed masking gratings of various spatial and temporal frequencies. A mask of similar spatial and temporal frequencies to the test grating reduces sensitivity considerably, whereas one differing greatly in spatial or temporal frequency has little or no effect. The results show that for test gratings drifting at 8 Hz, the tuning function is bandpass in both space and time, peaked at the temporal and spatial frequency (SF) of the test (SFs were 0.1, 1 or 5 c deg-1; c represents cycles throughout). For a grating of 5 c deg-1 drifting at 0.3 Hz, the function is bandpass in space but lowpass in time. Fourier transform of the frequency results yields a function in space-time which we term the 'spatiotemporal receptive field'. For movement detectors (bandpass in space and time) the fields comprise alternating ridges of opposing polarity, elongated in space-time along the preferred velocity axis of the detector. We suggest that this organization explains how detectors analyse form and motion concurrently and accounts, at least in part, for a variety of perceptual phenomena, including summation, reduction of motion smear, metacontrast, stroboscopic motion and spatiotemporal interpolation.

Differential Threshold↗

Smooth and sampled motion.

Stroboscopic or sampled motion is indistinguishable from smooth motion if the frequency of sampling is sufficiently high. We report measurements of the minimum sample frequency for smooth motion of drifting sinusoidal gratings (extended and truncated) which varied in spatial frequency from 0.06 to 24 c/deg, in temporal frequency from 1.5 to 24 Hz and in contrast from 3 to 100 times detection threshold. Threshold sampling frequency for smoothness increased with temporal frequency and contrast, and inversely with spatial frequency. The threshold step size associated with the sampling frequency ranged from 20" arc (for gratings of 24 c/deg) to 6 deg (for gratings of 0.06 c/deg). Calculations of the spurious frequencies introduced by sampling lead us to conclude that motion appears smooth provided that sampling is above the Nyquist limit and that the amplitude of the spurious components is below their independent threshold.

Humans↗

Local and global visual processing.

The fundamental sinusoidal components of a chequerboard pattern are oriented at 45 degrees to the orientation of the chequerboard edges. Removal of one of the fundamental sinusoids (at +45 degrees) creates a useful pattern for studying the mechanisms of visual analysis. Close up, the pattern appears to be oriented +45 degrees, although there is no global energy at that orientation, implying local analysis. At a distance, the perceived diagonality switches to -45 degrees implying access to global information. Measurements show that contrast thresholds for seeing diagonality at +45 degrees follow closely those for detecting the 5th harmonic component of the pattern, over a wide range of spatial frequencies and luminances. Low pass filtering also causes the pattern to be perceived according to its global energy, provided that the cutoff frequency is set to remove the fifth harmonic. We conclude that, at least for this particular stimulus, the visual system performs a local analysis if the fifth harmonic is visible and a global analysis if not.

Form Perception↗

A spatial illusion from motion rivalry.

A new dynamic visual illusion is reported: contrast reversal of a horizontal and vertical plaid pattern (produced by adding two orthogonal sinusoidal gratings) causes the pattern to appear as an array of lustrous diamonds, cut by sharp lines into a diagonal lattice structure. On the basis of computer simulations it is suggested that the illusion results from rivalrous interaction of motion detectors tuned to opposing directions of motion.

Humans↗

Recognition of positive and negative bandpass-filtered images.

A study is reported in which the significance for vision of low- and high-spatial-frequency components of photographic positive and negative images was investigated by measuring recognition of bandpass-filtered photographs of faces. The results show that a 1.5 octave bandpass-filtered image contains sufficient visual information for good recognition performance, provided the filter is centred close to 20 cycles facewidth-1. At low spatial frequencies negatives are more difficult to recognize than positives, but at high spatial frequencies there is no difference in recognition, implying that it is the low-frequency components of negatives which present difficulties for the visual system.

Color Perception↗

Spatial and temporal properties of neurons of the lateral suprasylvian cortex of the cat.

Neurons in the posteromedial lateral suprasylvian cortex (PMLS) of cats were recorded extracellularly to investigate their response to stimulation by bars and by sinusoidal gratings. Two general types of cells were identified: those that modulated in synchrony with the passage of drifting bars and gratings and those that responded with an unmodulated increase in discharge. Both types responded to contrast reversed gratings with a modulation of activity: the cells that modulated to drifting gratings modulated to the first harmonic of contrast reversed gratings (at appropriate spatial phase and frequency), whereas those that did not modulate to drifting gratings always modulated to the second harmonic of contrast reversed gratings. No cell had a clear null point. Nearly all cells were selective for spatial frequency. The preferred frequency ranged from 0.1 to 1 cycles per degree (cpd), and selectivity bandwidths (full width at half height) were around two octaves. Preferred spatial frequency was not correlated with receptive field size, but bandwidth and receptive field size were positively correlated. Preferred spatial frequency decreased with eccentricity, at about 0.05 octaves/deg. The response of all cells increased as a function of grating contrast up to a saturation level. The contrast threshold for response to a grating of optimal parameters was approximately 1% for most cells and the saturation contrast approximately 10%. The contrast gain was approximately 25 spikes/s per log unit of contrast. All cells were tuned for temporal frequency, preferring frequencies from approximately 3 to 10 Hz, with a selectivity bandwidth approximately 2 octaves. For some cells, the spatial selectivity did not depend on the temporal frequency and vice versa. Others were spatiotemporally coupled, with the preferred temporal frequency being lower at high than at low spatial frequencies, and the preferred spatial frequency lower at high than at low temporal frequencies. Previous results showing broad velocity tuning to a bar were replicated and found to be predictable from the combined spatial and temporal tuning of PMLS cells and the Fourier spectrum of a bar. Preferred temporal frequency steadily decreased with eccentricity, at 0.025 octaves/deg. The results for PMLS cells are compared with those of other visual areas. Acuity and spatial preference and selectivity bandwidth is comparable to all areas except area 17, where they are a factor of about two higher. Temporal selectivity in PMLS is as fine as observed in other areas. The possibility that PMLS cells may be involved with motion detection and detection of motion in depth is discussed.

Animals↗

Visual acuity of neurones in the cat lateral suprasylvian cortex.

The spatial acuity was measured for cells of the posteromedial lateral suprasylvian area (PMLS) of the cat. Acuities were found to be 2 cycles/degree (15 mins arc) at best, and 1 cycle/degree (30 mins arc) on average. Both best acuity and average acuity remained constant with receptive field eccentricity within 20 degrees of the area centralis, and then fell gradually with eccentricity. Acuity was good, given receptive field size, and was not correlated with receptive field size. Comparisons are drawn with other visual structures.

Animals↗

Spatial and temporal selectivity of the human motion detection system.

Measurements were made of spatial frequency, orientation and temporal frequency selectivity of the visual motion system. The results suggest: (1) There exists in the motion system mechanisms selective for spatial frequency. The preferred spatial frequency varies considerably and extends down to at least 0.06 c/deg. (2) At all spatial frequencies (from 0.1 to 10 c/deg) there exist detectors selective for orientation which vary in (directed) orientation tuning to encompass 360 degrees. (3) The bandwidth of both spatial frequency and orientation selectivity vary inversely with spatial frequency: the lower the spatial frequency, the broader the bandwidth. (4) There exist two classes of temporally tuned detectors, one lowpass (sustained) and one bandpass (transient), of preferred temporal frequency of 7-13 Hz (depending on spatial frequency).

Form Perception↗