Predictions of U-Shaped Backward Pattern Masking from Considerations of the Spatio-Temporal Frequency Response

Perception ◽  
1975 ◽  
Vol 4 (3) ◽  
pp. 297-304 ◽  
Author(s):  
Bruno G Breitmeyer

The threshold detectability of a briefly presented target stimulus consisting of a vertical sinusoidal grating was affected not only by the spatial frequency content of an equally briefly presented, two-octave-wide masking noise, but also by the time interval separating the onsets of the target and its mask. Over a range of stimulus onset asynchronies, in which the mask onset either preceded, coincided with, or followed the target onset, a mask with a low spatial frequency content had its greatest masking effect on a high spatial frequency target grating when the mask followed the target by 120–180 ms. When the mask had a high spatial frequency content and the target was of low spatial frequency, or when the target was entered on the mask frequency band, optimal masking effects occurred when the onsets of the mask and target coincided. The results are discussed in relation to previous masking studies, particuarly those in which U-shaped backward pattern masking functions are obtained.

Author(s):  
Peter Cawley

Abstract Permanently installed SHM systems are now a viable alternative to traditional periodic inspection (NDT). However, their industrial use is limited and this paper reviews the steps required in developing practical SHM systems. The transducers used in SHM are fixed in location, whereas in NDT they are generally scanned. The aim is to reach similar performance with high temporal frequency, low spatial frequency SHM data to that achievable with conventional high spatial frequency, low temporal frequency NDT inspections. It is shown that this can be done via change tracking algorithms such as the Generalized Likelihood Ratio (GLR) but this depends on the input data being normally distributed, which can only be achieved if signal changes due to variations in the operating conditions are satisfactorily compensated; there has been much recent progress on this topic and this is reviewed. Since SHM systems can generate large volumes of data, it is essential to convert the data to actionable information, and this step must be addressed in SHM system design. It is also essential to validate the performance of installed SHM systems, and a methodology analogous to the model assisted POD (MAPOD) scheme used in NDT has been proposed. This uses measurements obtained from the SHM system installed on a typical undamaged structure to capture signal changes due to environmental and other effects, and to superpose the signal due to damage growth obtained from finite element predictions. There is a substantial research agenda to support the wider adoption of SHM and this is discussed.


Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 362-362
Author(s):  
R J Snowden

Peripheral vision has been modelled as a coarser version of foveal vision. Thus visual behaviour elicited by, say, a 2 cycles deg−1 grating imaged foveally would be reproduced in the periphery by a lower spatial frequency (say 1 cycle deg−1). Tuning for orientation is broader at a low than high spatial frequency (Snowden, 1992 Vision Research32 1965 – 1974). Taken together this leads to the surprising prediction that, given a particular spatial frequency, tuning for orientation is narrower for peripheral viewing! In this study it has also been found that orientation tuning broadens with increasing temporal frequency, but the opposite relationship has been reported for peripheral vision (Sharpe and Tolhurst, 1973 Vision Research13 2103 – 2112). Orientation bandwidths were measured by the method of selective adaptation following the procedures and analysis techniques described by Snowden (1991 Proceedings of the Royal Society of London, Series B246 53 – 59). The results show that orientation bandwidths did indeed narrow as a stimulus was imaged more peripherally, so that its bandwidth in the peripheral retina could be half that of the fovea. However, at a greater eccentricity, bandwidths broadened once more. The results were not influenced by the contrast of the adaptation pattern eliminating visibility as a possible explanation. Increasing temporal frequency broadened orientation bandwidth at all eccentricities.


1986 ◽  
Vol 56 (5) ◽  
pp. 1321-1354 ◽  
Author(s):  
F. A. Miles ◽  
K. Kawano ◽  
L. M. Optican

The ocular following responses elicited by brief unexpected movements of the visual scene were studied in 10 rhesus monkeys. Test patterns were either random dots or sine-wave gratings [spatial frequency (Fs) 0.046-1.06 cycles per degree (c/degree)]. Test stimuli were velocity steps [speed (V) 5-400 degrees/s] of 100-ms duration, applied 50 ms after spontaneous saccades to avoid saccadic intrusions. Eye velocity response profiles were nonmonotonic and idiosyncratic, but consistent and closely time-locked to stimulus onset. Two measures of response amplitude were used: initial peak in eye velocity (ei), and average final eye velocity over the period of 110-140 ms measured from stimulus onset (ef). Using random dot patterns, response latencies were short, e.g., when the criterion for onset was an eye acceleration of 100 degrees/s2, mean latency (+/- SE) for eight monkeys with a 40 degrees/s test ramp was 51.5 +/- 0.6 ms. Using gratings of low spatial frequency (Fs less than 0.5 c/degree), latency was inversely related to, and solely a function of, contrast and temporal frequency, Ft (where Ft = V X Fs). We conclude from the latter that ocular following is triggered by local changes in luminance, and propose a model of the detection mechanism that reproduces all the essential features of these data. Moderate low-pass spatial filtering ("blurring") of the random dot pattern, by interposing a sheet of ground glass between the animal and the scene, progressively increased the response latency and decreased ef, but ei was either little affected or increased. When used with gratings, the ground glass simply reduced the contrast (range: 0.5-0.003), with very similar consequences for ocular following: latency increased and ef decreased, but ei changed little over the first decade of contrast reduction, increased over the second, and began to show attenuation (often pronounced) only at the lowest contrast. We suggest that these anomalous increases in ei with reductions in contrast are secondary to the delay in response onset and might be explained if the motion detectors responsible for triggering ocular following act as a gate for integrated retinal slip inputs to the tracking system proper: the delay in detection causes a buildup in the error signal driving the tracking response. En masse movement of the visual field was not the optimal stimulus for ocular following.(ABSTRACT TRUNCATED AT 400 WORDS)


2001 ◽  
Vol 85 (4) ◽  
pp. 1512-1521 ◽  
Author(s):  
N.S.C. Price ◽  
M. R. Ibbotson

The visual response properties of nondirectional wide-field sensitive neurons in the wallaby pretectum are described. These neurons are called scintillation detectors (SD-neurons) because they respond vigorously to rapid, high contrast visual changes in any part of their receptive fields. SD-neurons are most densely located within a 1- to 2-mm radius from the nucleus of the optic tract, interspersed with direction-selective retinal slip cells. Receptive fields are monocular and cover large areas of the contralateral visual field (30–120°). Response sizes are equal for motion in all directions, and spontaneous activities are similar for all orientations of static sine-wave gratings. Response magnitude increases near linearly with increasing stimulus diameter and contrast. The mean response latency for wide-field, high-contrast motion stimulation was 43.4 ± 9.4 ms (mean ± SD, n = 28). The optimum visual stimuli for SD-neurons are wide-field, low spatial frequency (<0.2 cpd) scenes moving at high velocities (75–500°/s). These properties match the visual input during saccades, indicating optimal sensitivity to rapid eye movements. Cells respond to brightness increments and decrements, suggesting inputs from on and off channels. Stimulation with high-speed, low spatial frequency gratings produces oscillatory responses at the input temporal frequency. Conversely, high spatial frequency gratings give oscillations predominantly at the second harmonic of the temporal frequency. Contrast reversing sine-wave gratings elicit transient, phase-independent responses. These responses match the properties of Y retinal ganglion cells, suggesting that they provide inputs to SD-neurons. We discuss the possible role of SD-neurons in suppressing ocular following during saccades and in the blink or saccade-locked modulation of lateral geniculate nucleus activity to control retino-cortical information flow.


1990 ◽  
Vol 5 (04) ◽  
pp. 321-346 ◽  
Author(s):  
Peter H. Schiller ◽  
Nikos K. Logothetis ◽  
Eliot R. Charles

AbstractThe functions of the primate color-opponent and broad-band channels were assessed by examining the visual capacities of rhesus monkeys following selective lesions of parvocellular and magnocellular lateral geniculate nucleus, which respectively relay these two channels to the cortex. Parvocellular lesions impaired color vision, high spatial-frequency form vision, and fine stereopsis. Magnocellular lesions impaired high temporal- frequency flicker and motion perception but produced no deficits in stereopsis. Low spatial-frequency form vision, stereopsis, and brightness perception were unaffected by either lesion. Much as the rods and cones of the retina can be thought of as extending the range of vision in the intensity domain, we propose that the color-opponent channel extends visual capacities in the wavelength and spatial-frequency domains whereas the broad-band channel extends them in the temporal domain.


2005 ◽  
Vol 55 (3) ◽  
pp. 245-258 ◽  
Author(s):  
◽  
◽  
◽  

AbstractFlickering light can cause adverse effects in some humans, as can rhythmic spatial patterns of particular frequencies. We investigated whether birds react to the temporal frequency of standard 100 Hz fluorescent lamps and the spatial frequency of the visual surround in the manner predicted by the human literature, by examining their effects on the preferences, behaviour and plasma corticosterone of European starlings (Sturnus vulgaris). We predicted that high frequency lighting (> 30 kHz) and a relatively low spatial frequency on the walls of their cages (0.1 cycle cm−1) would be less aversive than low frequency lighting (100 Hz) and a relatively high spatial frequency (2.5 cycle cm−1). Birds had strong preferences for both temporal and spatial frequencies. These preferences did not always fit with predictions, although there was evidence that 100 Hz was more stressful than 30 kHz lighting, as birds were less active and basal corticosterone levels were higher under 100 Hz lighting. Our chosen spatial frequencies had no overall significant effect on corticosterone levels. Although there are clearly effects of, and interactions between, the frequency of the light and the visual surround on the behaviour and physiology of birds, the pattern of results is not straightforward.


2021 ◽  
Vol 2 ◽  
Author(s):  
Arthur Shapiro

Shapiro and Hedjar (2019) proposed a shift in the definition of illusion, from ‘differences between perception and reality’ to ‘conflicts between possible constructions of reality’. This paper builds on this idea by presenting a series of motion hybrid images that juxtapose fine scale contrast (high spatial frequency content) with coarse scale contrast-generated motion (low spatial frequency content). As is the case for static hybrid images, under normal viewing conditions the fine scale contrast determines the perception of motion hybrid images; however, if the motion hybrid image is blurred or viewed from a distance, the perception is determined by the coarse scale contrast. The fine scale contrast therefore masks the perception of motion (and sometimes depth) produced by the coarser scale contrast. Since the unblurred movies contain both fine and coarse scale contrast information, but the blurred movies contain only coarse scale contrast information, cells in the brain that respond to low spatial frequencies should respond equally to both blurred and unblurred movies. Since people undoubtedly differ in the optics of their eyes and most likely in the neural processes that resolve conflict across scales, the paper suggests that motion hybrid images illustrate trade-offs between spatial scales that are important for understanding individual differences in perceptions of the natural world.


Perception ◽  
1982 ◽  
Vol 11 (5) ◽  
pp. 505-528 ◽  
Author(s):  
David Rose ◽  
Ivan Lowe

An investigation has been made into the temporal parameters with which the detection threshold for a sinusoidal grating changes during and after adaptation to the same grating at high contrast. Stationary high-spatial-frequency gratings and a phase-reversing low-spatial-frequency grating have been studied separately. It was found that the threshold continues to rise during adaptation for at least 6 min without sign of levelling off, and that full recovery from 6 min of adaptation can take more than 45 min. Intermittent adaptation and continuous adaptation for the same period produce similar effects. Single-phase and dual-phase exponential fits to the data are rejected, and it is concluded that the level of adaptation of the visual system to spatial contrast changes as a power function of time. However, recovery is not always monotonic, especially after adaptation to phase-reversing gratings. This may be due to inhibitory interactions between channels (in particular, those for pattern and movement information).


1989 ◽  
Vol 3 (6) ◽  
pp. 563-572 ◽  
Author(s):  
John A. Baro ◽  
Stephen Lehmkuhle

AbstractAveraged grating-evoked cortical potentials were recorded from area 17 of awake cats. Peak latency of early components of the visual-evoked potential (VEP) response to stimulus onset increased as a function of spatial frequency, while amplitude tended to be largest at intermediate spatial frequencies. Latency increased and amplitude generally decreased to lower spatial-frequency stimuli (<0.25 cycle/deg) in the presence of a uniform flickering field (UFF). The UFF had a relatively small or opposite effect on peak latency and amplitude for higher spatial-frequency stimuli (>0.50 cycle/deg). The VEP response to stimulus offset was present only at low spatial frequencies and was virtually eliminated by the presence of the UFF. The effects were similar whether the target and UFF background were simultaneously presented or briefly separated; however, the UFF had no effect when the two were spatially separated. The effects of the UFF background on VEP onset response increased with increasing temporal frequency from 2–8 Hz; offset responses were affected similarly at all temporal frequencies. These effects are similar to those observed in humans and suggest that two spatio-temporally tuned mechanisms contribute to the early VEP response. In the cat, the mechanisms seem to correspond to X and Y cells in the dorsal lateral geniculate nucleus.


Sign in / Sign up

Export Citation Format

Share Document