Temporal and Spatial Frequency Tuning of the Flicker Motion Aftereffect

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 12-12
Author(s):  
P J Bex ◽  
F A J Verstraten ◽  
I Mareschal
Keyword(s):  
Spatial Frequency ◽  
Frequency Tuning ◽  
Temporal Frequency ◽  
Motion Aftereffect ◽  
Sine Wave ◽  
Test Grating ◽  
Spatial Frequency Tuning ◽  
Spatial Frequencies ◽  
Low Pass ◽  
Sine Wave Gratings

The motion aftereffect (MAE) was used to study the temporal-frequency and spatial-frequency selectivity of the visual system at suprathreshold contrasts. Observers adapted to drifting sine-wave gratings of a range of spatial and temporal frequencies. The magnitude of the MAE induced by the adaptation was measured with counterphasing test gratings of a variety of spatial and temporal frequencies. Independently of the spatial or temporal frequency of the adapting grating, the largest MAE was found with slowly counterphasing test gratings (∼0.125 – 0.25 Hz). For slowly counterphasing test gratings (<∼2 Hz), the largest MAEs were found when the test grating was of similar spatial frequency to that of the adapting grating, even at very low spatial frequencies (0.125 cycle deg−1). However, such narrow spatial frequency tuning was lost when the temporal frequency of the test grating was increased. The data suggest that MAEs are dominated by a single, low-pass temporal-frequency mechanism and by a series of band-pass spatial-frequency mechanisms at low temporal frequencies. At higher test temporal frequencies, the loss of spatial-frequency tuning implicates separate mechanisms with broader spatial frequency tuning.

Figure and Ground in Space and Time: 2. Frequency, Velocity, and Perceptual Organization

Perception ◽  
1989 ◽  
Vol 18 (5) ◽  
pp. 639-648 ◽  
Author(s):  
Victor Klymenko ◽  
Naomi Weisstein
Keyword(s):  
Spatial Frequency ◽  
Temporal Frequency ◽  
Sine Wave ◽  
Stationary Condition ◽  
Velocity Difference ◽  
Lower Spatial Frequency ◽  
Spatial Frequencies ◽  
Spatiotemporal Tuning ◽  
Sine Wave Gratings ◽  
Ground Organization

The figure – ground organization of an ambiguous bipartite pattern in which the two regions of the pattern contained sine-wave gratings which differed in spatial frequency was examined for two pairs of spatial frequencies: 1 and 4 cycles deg−1, and 1 and 8 cycles deg−1. The region of higher spatial frequency underwent contrast reversal at one of four rates: 0, 3.75, 7.5, or 15 Hz. The region of lower spatial frequency was equated with either the temporal frequency or the velocity of the grating of higher spatial frequency in three sets of conditions: one stationary condition, three in which temporal frequency was equated, and three in which velocity was equated. For the 1 and 4 cycles deg−1 pair, the region of lower spatial frequency tended to be seen as the background a higher percentage of the time. There were significant linear trends for the appearance as background of the region of lower spatial frequency with respect to the magnitude of the velocity difference between the two regions of the pattern. The faster the 1 cycle deg−1 grating moved with respect to the 4 cycles deg−1 grating, the higher the percentage of the time it was seen as the ground. The results for the 1 and 8 cycles deg−1 pair were in some cases unexpected in that the 8 cycles deg−1 grating was seen as the ground behind the 1 cycle deg−1 grating even though it was of a higher spatial frequency and moved at a slower velocity. The spatiotemporal tuning of the visual system is discussed.

Effects of Experience on Spatial Frequency Tuning in the Visual System: Behavioral, Visuocortical, and Alpha-band Responses

2020 ◽  
Vol 32 (6) ◽  
pp. 1153-1169 ◽  
Author(s):  
Wendel M. Friedl ◽  
Andreas Keil
Keyword(s):  
Spatial Frequency ◽  
Undergraduate Students ◽  
Frequency Tuning ◽  
Temporal Frequency ◽  
Alpha Power ◽  
Alpha Band ◽  
Conditioning Paradigm ◽  
Spatial Frequency Tuning ◽  
Spatial Frequencies ◽  
Time Courses

Using electrophysiology and a classic fear conditioning paradigm, this work examined adaptive visuocortical changes in spatial frequency tuning in a sample of 50 undergraduate students. High-density EEG was recorded while participants viewed 400 total trials of individually presented Gabor patches of 10 different spatial frequencies. Patches were flickered to produce sweep steady-state visual evoked potentials (ssVEPs) at a temporal frequency of 13.33 Hz, with stimulus contrast ramping up from 0% to 41% Michelson over the course of each 2800-msec trial. During the final 200 trials, a selected range of Gabor stimuli (either the lowest or highest spatial frequencies, manipulated between participants) were paired with an aversive 90-dB white noise auditory stimulus. Changes in spatial frequency tuning from before to after conditioning for paired and unpaired gratings were evaluated at the behavioral and electrophysiological level. Specifically, ssVEP amplitude changes were evaluated for lateral inhibition and generalization trends, whereas change in alpha band (8–12 Hz) activity was tested for a generalization trend across spatial frequencies, using permutation-controlled F contrasts. Overall time courses of the sweep ssVEP amplitude envelope and alpha-band power were orthogonal, and ssVEPs proved insensitive to spatial frequency conditioning. Alpha reduction (blocking) was most pronounced when viewing fear-conditioned spatial frequencies, with blocking decreasing along the gradient of spatial frequencies preceding conditioned frequencies, indicating generalization across spatial frequencies. Results suggest that alpha power reduction—conceptually linked to engagement of attention and alertness/arousal mechanisms—to fear-conditioned stimuli operates independently of low-level spatial frequency processing (indexed by ssVEPs) in primary visual cortex.

Figure and Ground in Space and Time: 1. Temporal Response Surfaces of Perceptual Organization

Perception ◽  
1989 ◽  
Vol 18 (5) ◽  
pp. 627-637 ◽  
Author(s):  
Victor Klymenko ◽  
Naomi Weisstein
Keyword(s):  
Spatial Frequency ◽  
Temporal Frequency ◽  
Sine Wave ◽  
Response Surfaces ◽  
Viewing Time ◽  
Temporal Response ◽  
Frequency Condition ◽  
Spatial Frequencies ◽  
Sine Wave Gratings ◽  
Ground Organization

The figure – ground organization of an ambiguous bipartite pattern can be manipulated by altering the temporal-frequency content of the two regions of the pattern. Ambiguous patterns in which the two regions of each pattern contained sine-wave gratings of either 8, 4, 1, or 0.5 cycles deg−1 undergoing contrast reversal at rates of 0, 3.75, 7.5, or 15 Hz were tested for figure–ground organization under conditions of equated space-averaged and time-averaged luminance and perceived contrast. All combinations of temporal-frequency differences between the two regions were tested at each spatial frequency. The data are reported for two levels of temporal resolution (15 and 30 s). The pattern region with the relatively higher temporal frequency tended to be seen as the background a higher percentage of the viewing time. There were significant linear trends for the appearance as background of the region of higher temporal frequency with respect to the magnitude of the temporal-frequency difference between the two regions of each pattern for all spatial frequencies and data intervals except the final 15 s interval of the lowest (0.5 cycle deg−1) spatial-frequency condition.

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.

Short-Term Memory for Speed

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 156-156
Author(s):  
P Thompson ◽  
R Stone ◽  
E Walton
Keyword(s):  
Spatial Frequency ◽  
Short Term Memory ◽  
Temporal Frequency ◽  
Frequency Discrimination ◽  
Sine Wave ◽  
Short Term ◽  
Term Memory ◽  
Visual Short Term Memory ◽  
Speed Discrimination ◽  
Sine Wave Gratings

We have measured the retention of information about stimulus speed in visual short-term memory by measuring speed discrimination in a two-interval forced-choice task. We have also measured such discrimination in conditions where a ‘memory masker’ is presented during the interstimulus interval (ISI) in a fashion analogous to the experiment of Magnussen et al (1991 Vision Research31 1213 – 1219). Magnussen et al found that spatial frequency discrimination was disrupted when the mask had a spatial frequency that differed from the test spatial frequency by an octave or more. We have investigated the speed discrimination of 8 Hz, 1 cycle deg−1 drifting sine-wave gratings with the following drifting masks presented in the ISI: (i) 8 Hz 1 cycle deg−1, same direction as the test; (ii) 8 Hz, 8 cycles deg−1, opposite direction to the test; (iii) 8 Hz, 8 cycles deg−1, same direction as the test; (iv) 24 Hz, 3 cycles deg−1, same direction as the test. These masks were chosen to investigate whether the temporal frequency, the spatial frequency, the speed, or the direction of motion of the mask affected retention. We found that in none of these conditions was the discrimination of the test gratings impaired significantly. This pattern of results is therefore different from that found with spatial frequency discrimination and suggests that, whatever mechanism is responsible for the retention of information about speed, it is different from that responsible for the retention of information about spatial frequency.

Stages of Orientation Coding Assessed by the Tilt Aftereffect

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 70-70
Author(s):  
R Anderson ◽  
M A Georgeson
Keyword(s):  
Spatial Frequency ◽  
Frequency Tuning ◽  
Broad Band ◽  
Tilt Aftereffect ◽  
Staircase Procedure ◽  
Test Grating ◽  
Spatial Frequency Tuning ◽  
Adaptation Condition ◽  
Parallel Condition

We investigated orientation coding via the spatial-frequency tuning of the tilt aftereffect (TAE). In the single-adaptation condition, subjects adapted to single gratings of 1 or 8 cycles deg−1, 40% contrast, tilted 15° clockwise or anticlockwise from vertical; in two double-adaptation conditions the 1 and 8 cycles deg−1 gratings were superimposed at opposite orientations (‘plaid’ condition) or at the same orientation (‘parallel’ condition). Test gratings of 1, 2, 4, and 8 cycles deg−1, 20% contrast, were presented for 150 ms in an interleaved staircase procedure that measured the TAE by nulling it, hence making a tilted test grating appear vertical. Initial adaptation was for 3 min, topped up for 2 s between test presentations. Results from the single-grating condition indicated broad spatial-frequency tuning of the TAE, since the effect was still strong when tested three octaves away from the adapter. In the parallel condition, the TAEs were around the average of those reported in the single condition. Negligible TAEs were found in the 1+8 cycles deg−1 plaid condition, indicating that opposing adaptations had effectively cancelled each other out. These findings strengthen the suggestion of Olzak and Thomas (1992 Vision Research32 1885 – 1898) that orientation is encoded via an integrative mechanism which pools or sums the outputs of different spatial-frequency channels, and further imply that much of the adaptation responsible for the TAE occurs at this later broad-band stage.

How Reliable is the Pattern Adaptation Technique? A Modeling Study

2009 ◽  
Vol 102 (4) ◽  
pp. 2245-2252 ◽  
Author(s):  
Jay Hegdé
Keyword(s):  
Spatial Frequency ◽  
Frequency Tuning ◽  
Spatial Vision ◽  
Neural Mechanisms ◽  
System Level ◽  
Sinusoidal Grating ◽  
Tuning Parameters ◽  
Neuronal Ensemble ◽  
Spatial Frequency Tuning ◽  
Spatial Frequencies

Upon prolonged viewing of a sinusoidal grating, the visual system is selectively desensitized to the spatial frequency of the grating, while the sensitivity to other spatial frequencies remains largely unaffected. This technique, known as pattern adaptation, has been so central to the psychophysical study of the mechanisms of spatial vision that it is sometimes referred to as the “psychologist's microelectrode.” While this approach implicitly assumes that the adaptation behavior of the system is diagnostic of the corresponding underlying neural mechanisms, this assumption has never been explicitly tested. We tested this assumption using adaptation bandwidth, or the range of spatial frequencies affected by adaptation, as a representative measure of adaptation. We constructed an intentionally simple neuronal ensemble model of spatial frequency processing and examined the extent to which the adaptation bandwidth at the system level reflected the bandwidth at the neuronal level. We find that the adaptation bandwidth could vary widely even when all spatial frequency tuning parameters were held constant. Conversely, different spatial frequency tuning parameters were able to elicit similar adaptation bandwidths from the neuronal ensemble. Thus, the tuning properties of the underlying units did not reliably reflect the adaptation bandwidth at the system level, and vice versa. Furthermore, depending on the noisiness of adaptation at the neural level, the same neuronal ensemble was able to produce selective or nonselective adaptation at the system level, indicating that a lack of selective adaptation at the system level cannot be taken to mean a lack of tuned mechanisms at the neural level. Together, our results indicate that pattern adaptation cannot be used to reliably estimate the tuning properties of the underlying units, and imply, more generally, that pattern adaptation is not a reliable tool for studying the neural mechanisms of pattern analysis.

scholarly journals Dynamics of spatial frequency tuning in mouse visual cortex

2012 ◽  
Vol 107 (11) ◽  
pp. 2937-2949 ◽  
Author(s):  
Samme Vreysen ◽  
Bin Zhang ◽  
Yuzo M. Chino ◽  
Lutgarde Arckens ◽  
Gert Van den Bergh
Keyword(s):  
Visual Cortex ◽  
Spatial Frequency ◽  
Visual Information ◽  
Frequency Tuning ◽  
Neuronal Response ◽  
Correlation Technique ◽  
Low Frequencies ◽  
Temporal Shift ◽  
Spatial Frequency Tuning ◽  
Spatial Frequencies

Neuronal spatial frequency tuning in primary visual cortex (V1) substantially changes over time. In both primates and cats, a shift of the neuron's preferred spatial frequency has been observed from low frequencies early in the response to higher frequencies later in the response. In most cases, this shift is accompanied by a decreased tuning bandwidth. Recently, the mouse has gained attention as a suitable animal model to study the basic mechanisms of visual information processing, demonstrating similarities in basic neuronal response properties between rodents and highly visual mammals. Here we report the results of extracellular single-unit recordings in the anesthetized mouse where we analyzed the dynamics of spatial frequency tuning in V1 and the lateromedial area LM within the lateral extrastriate area V2L. We used a reverse-correlation technique to demonstrate that, as in monkeys and cats, the preferred spatial frequency of mouse V1 neurons shifted from low to higher frequencies later in the response. However, this was not correlated with a clear selectivity increase or enhanced suppression of responses to low spatial frequencies. These results suggest that the neuronal connections responsible for the temporal shift in spatial frequency tuning may considerably differ between mice and monkeys.

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