Spatial Frequency-Specific Contrast Adaptation Originates in the Primary Visual Cortex

2007 ◽  
Vol 98 (1) ◽  
pp. 187-195 ◽  
Author(s):  
Thang Duong ◽  
Ralph D. Freeman

Adaptation to a high-contrast grating stimulus causes reduced sensitivity to subsequent presentation of a visual stimulus with similar spatial characteristics. This behavioral finding has been attributed by neurophysiological studies to processes within the visual cortex. However, some evidence indicates that contrast adaptation phenomena are also found in early visual pathways. Adaptation effects have been reported in retina and lateral geniculation nucleus (LGN). It is possible that these early pathways could be the physiological origin of the cortical adaptation effect. To study this, we recorded from single neurons in the cat's LGN. We find that contrast adaptation in the LGN, unlike that in the visual cortex, is not spatial frequency specific, i.e., adaptation effects apply to a broad range of spatial frequencies. In addition, aside from the amplitude attenuation, the shape of spatial frequency tuning curves of LGN cells is not affected by contrast adaptation. Again, these findings are unlike those found for cells in the visual cortex. Together, these results demonstrate that pattern specific contrast adaptation is a cortical process.

1990 ◽  
Vol 4 (05) ◽  
pp. 413-426 ◽  
Author(s):  
M.A. Berkley

AbstractAn aftereffects paradigm was used to behaviorally measure contrast sensitivity of cats to gratings of three different test spatial frequencies after adaptation to gratings of various spatial frequencies, contrasts, and durations. Post-adaptation reductions in sensitivity occurred even after short periods of adaptation (<7 s) and could be as large as 1.0 log unit under some conditions. The magnitude of the adaptation effect varied monotonically with (1) adaptation grating contrast, (2) duration, and (3) the contrast sensitivity for the test grating. Average half-width (at half-height) of the spatial-frequency tuning curves constructed from the data was 1.4 octaves, and was not dependent upon the level of adaptation or the spatial frequency of the test grating. Post-adaptation psychometric functions of the cats showed reduced slopes and maxima suggesting that, unlike humans, in cats apparent contrast grows more slowly with increases in physical contrast after contrast adaptation. All of the characteristics observed are in excellent agreement with electrophysiologically measured properties of neurons in striate cortex of cats. In addition, there was a remarkable similarity of the cat tuning functions, both in shape and bandpass, to those measured in man with a similar paradigm suggesting that (1) the two visual systems are sufficiently similar to make the cat a useful spatial vision model and (2) there is a common functional plan to all mammalian visual systems despite significant anatomical differences between species.


2012 ◽  
Vol 107 (11) ◽  
pp. 2937-2949 ◽  
Author(s):  
Samme Vreysen ◽  
Bin Zhang ◽  
Yuzo M. Chino ◽  
Lutgarde Arckens ◽  
Gert Van den Bergh

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.


2021 ◽  
Author(s):  
Felix Bartsch ◽  
Bruce G Cumming ◽  
Daniel A Butts

To understand the complexity of stimulus selectivity in primary visual cortex (V1), models constructed to match observed responses to complex time-varying stimuli, instead of to explain responses to simple parametric stimuli, are increasingly used. While such models often can more accurately reflect the computations performed by V1 neurons in more natural visual environments, they do not by themselves provide insight into established measures of V1 neural selectivity such as receptive field size, spatial frequency tuning and phase invariance. Here, we suggest a series of analyses that can be directly applied to encoding models to link complex encoding models to more interpretable aspects of stimulus selectivity, applied to nonlinear models of V1 neurons recorded in awake macaque in response to random bar stimuli. In linking model properties to more classical measurements, we demonstrate several novel aspects of V1 selectivity not available to simpler experimental measurements. For example, we find that individual spatiotemporal elements of the V1 models often have a smaller spatial scale than the overall neuron sensitivity, and that this results in non-trivial tuning to spatial frequencies. Additionally, our proposed measures of nonlinear integration suggest that more classical classifications of V1 neurons into simple versus complex cells are spatial-frequency dependent. In total, rather than obfuscate classical characterizations of V1 neurons, model-based characterizations offer a means to more fully understand their selectivity, and provide a means to link their classical tuning properties to their roles in more complex, natural, visual processing.


1981 ◽  
Vol 213 (1191) ◽  
pp. 183-199 ◽  

The amplitudes of the responses of over 300 neurons in area 17 of the cat were examined as a function of the spatial frequency of moving sinusoidal gratings. The optimal spatial frequency and the bandwidth of the tuning curves were determined. The bandwidth varied considerably from neuron to neuron. Neurons optimally responsive to high spatial frequencies tended to have narrower tuning curves than those responsive to lower frequencies. Neurons with narrow spatial frequency tuning curves also tended to have narrow orientation tuning curves. These observations suggest that linear spatial summation tends to occur over a relatively constant area of visual field despite marked differences in each neuron’s optimal spatial frequency, a prediction of one model of visual analysis. There was little difference in either the optimal spatial frequencies or the bandwidths of tuning for different functional classes of neuron. Neurons with broad tuning curves tended to be restricted to lamina IV and its environs, being concentrated in the deep part of lamina II–III and the upper part of lamina IV ab. Neurons with very low optimal spatial frequencies were uncommon and tended to be found either at the border of laminae II–III and IV or in lamina V. These laminar distributions are discussed with respect to the laminar differences in the projection of l. g. n. X- and Y- cells to the visual cortex.


2021 ◽  
Author(s):  
William F. Broderick ◽  
Eero P. Simoncelli ◽  
Jonathan Winawer

AbstractNeurons in primate visual cortex (area V1) are tuned for spatial frequency, in a manner that depends on their position in the visual field. Several studies have examined this dependency using fMRI, reporting preferred spatial frequencies (tuning curve peaks) of V1 voxels as a function of eccentricity, but their results differ by as much as two octaves, presumably due to differences in stimuli, measurements, and analysis methodology. Here, we characterize spatial frequency tuning at a millimeter resolution within human primary visual cortex, across stimulus orientation and visual field locations. We measured fMRI responses to a novel set of stimuli, constructed as sinusoidal gratings in log-polar coordinates, which include circular, radial, and spiral geometries. For each individual stimulus, the local spatial frequency varies inversely with eccentricity, and for any given location in the visual field, the full set of stimuli span a broad range of spatial frequencies and orientations. Over the measured range of eccentricities, the preferred spatial frequency is well-fit by a function that varies as the inverse of the eccentricity plus a small constant. We also find small but systematic effects of local stimulus orientation, defined in both absolute coordinates and relative to visual field location. Specifically, peak spatial frequency is higher for tangential than radial orientations and for horizontal than vertical orientations.


1994 ◽  
Vol 11 (5) ◽  
pp. 939-951 ◽  
Author(s):  
Kirk G. Thompson ◽  
Audie G. Leventhal ◽  
Yifeng Zhou ◽  
Dan Liu

AbstractThe cortical contribution to the orientation and direction sensitivity of LGNd relay cells was investigated by recording the responses of relay cells to drifting sinusoidal gratings of varying spatial frequencies, moving bars, and moving spots in cats in which the visual cortex (areas 17, 18, 19, and LS) was ablated. For comparison, the spatial-frequency dependence of orientation and direction tuning of striate cortical cells was investigated employing the same quantitative techniques used to test LGNd cells. There are no significant differences in the orientation and direction tuning to relay cells in the LGNd of normal and decorticate cats. The orientation and direction sensitivities of cortical cells are dependent on stimulus parameters in a fashion qualitatively similar to that of LGNd cells. The differences in the spatial-frequency bandwidths of LGNd cells and cortical cells may explain many of their differences in orientation and direction tuning. Although factors beyond narrowness of spatial-frequency tuning must exist to account for the much stronger orientation and direction preferences of cells in area 17 when compared to LGNd cells, the evidence suggests that the orientation and direction biases present in the afferents to the visual cortex may contribute to the orientation and direction selectivities found in cortical cells.


1998 ◽  
Vol 15 (4) ◽  
pp. 585-595 ◽  
Author(s):  
CONG YU ◽  
DENNIS M. LEVI

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.


Some computational theories of motion perception assume that the first stage en route to this perception is the local estimate of image velocity. However, this assumption is not supported by data from the primary visual cortex. Its motion sensitive cells are not selective to velocity, but rather are directionally selective and tuned to spatio-temporal frequen­cies. Accordingly, physiologically based theories start with filters selec­tive to oriented spatio-temporal frequencies. This paper shows that computational and physiological theories do not necessarily conflict, because such filters may, as a population, compute velocity locally. To prove this point, we show how to combine the outputs of a class of frequency tuned filters to detect local image velocity. Furthermore, we show that the combination of filters may simulate ‘Pattern’ cells in the middle temporal area (MT), whereas each filter simulates primary visual cortex cells. These simulations include three properties of the primary cortex. First, the spatio-temporal frequency tuning curves of the in­dividual filters display approximate space-time separability. Secondly, their direction-of-motion tuning curves depend on the distribution of orientations of the components of the Fourier decomposition and speed of the stimulus. Thirdly, the filters show facilitation and suppression for responses to apparent motions in the preferred and null directions, respect­ively. It is suggested that the MT’s role is not to solve the aperture problem, but to estimate velocities from primary cortex information. The spatial integration that accounts for motion coherence may be postponed to a later cortical stage.


2020 ◽  
Vol 13 (2) ◽  
pp. 72-89
Author(s):  
D.S. Alekseeva ◽  
V.V. Babenko ◽  
D.V. Yavna

Visual perceptual representations are formed from the results of processing the input image in parallel pathways with different spatial-frequency tunings. It is known that these representations are created gradually, starting from low spatial frequencies. However, the order of information transfer from the perceptual representation to short-term memory has not yet been determined. The purpose of our study is to determine the principle of entering information of different spatial frequencies in the short-term memory. We used the task of unfamiliar faces matching. Digitized photographs of faces were filtered by six filters with a frequency tuning step of 1 octave. These filters reproduced the spatial-frequency characteristics of the human visual pathways. In the experiment, the target face was shown first. Its duration was variable and limited by a mask. Then four test faces were presented. Their presentation was not limited in time. The observer had to determine the face that corresponds to the target one. The dependence of the accuracy of the solution of the task on the target face duration for different ranges of spatial frequencies was determined. When the target stimuli were unfiltered (broadband) faces, the filtered faces were the test ones, and vice versa. It was found that the short-term memory gets information about an unfamiliar face in a certain order, starting from the medium spatial frequencies, and this sequence does not depend on the processing method (holistic or featural).


Perception ◽  
1973 ◽  
Vol 2 (1) ◽  
pp. 53-60 ◽  
Author(s):  
J A Movshon ◽  
C Blakemore

An adaptation method is used to determine the orientation specificity of channels sensitive to different spatial frequencies in the human visual system. Comparison between different frequencies is made possible by a data transformation in which orientational effects are expressed in terms of equivalent contrast (the contrast of a vertical grating producing the same adaptational effect as a high-contrast grating of a given orientation). It is shown that, despite great variances in the range of orientations affected by adaptation at different spatial frequencies (±10° to ±50°), the half-width at half-amplitude of the orientation channels does not vary systematically as a function of spatial frequency over the range tested (2·5 to 20 cycles deg−1). Two subjects were used and they showed significantly different orientation tuning across the range of spatial frequencies. The results are discussed with reference to previous determinations of orientation specificity, and to related psychophysical and neurophysiological phenomena.


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