Spatial and temporal response properties of residual vision in a case of hemianopia

1994 ◽  
Vol 343 (1304) ◽  
pp. 157-166 ◽  

Residual vision in subjects with damage of the primary visual cortex (striate cortex) has been demonstrated in many previous studies and is taken to reflect the properties of known subcortical and extrastriate visual pathways. In this report we describe psychophysical experiments carried out on a subject clinically blind in half of his visual field (i.e. homonymous hemianopia) caused by striate cortex dam age. They reveal the existence of two distinct channels mediating such vision. One channel responds to spatial structure and the other to light flux changes. The spatially tuned channel has a peak response at about 1.2 cycles per degree and shows rapid loss of sensitivity at both high and low spatial frequencies. This channel does not respond to diffuse illumination. The light flux channel, however, responds only to sudden increments in light flux levels on the retina and shows extensive spatial summation. Both channels require transient inputs, with a peak sensitivity at about 10 cycles per second and show virtually complete attenuation at temporal frequencies below 2 cycles per second. The spatiotemporal characteristics of these two channels account for much of the reported limits of visual performance attributed to subcortical or extrastriate pathways in some patients, and especially for their relatively good sensitivity for the detection of abrupt, transient stimuli or fast-moving targets. A new method is also applied to the m easurement of the amount of light scatter in the eye. The measurements show that light scatter into the sighted hemifield could not account for the results obtained with the stimuli used to characterize the residual vision of this subject.

1993 ◽  
Vol 69 (4) ◽  
pp. 1091-1117 ◽  
Author(s):  
G. C. DeAngelis ◽  
I. Ohzawa ◽  
R. D. Freeman

1. Most studies of cortical neurons have focused on the spatial structure of receptive fields. For a more complete functional description of these neurons, it is necessary to consider receptive-field structure in the joint domain of space and time. We have studied the spatiotemporal receptive-field structure of 233 simple cells recorded from the striate cortex of adult cats and kittens at 4 and 8 wk postnatal. The dual goal of this study is to provide a detailed quantitative description of spatiotemporal receptive-field structure and to compare the developmental time courses of spatial and temporal response properties. 2. Spatiotemporal receptive-field profiles have been measured with the use of a reverse correlation method, in which we compute the cross-correlation between a neuron's response and a random sequence of small, briefly presented bright and dark stimuli. The receptive-field profiles of some simple cells are space-time separable, meaning that spatial and temporal response characteristics can be dissociated. Other cells have receptive-field profiles that are space-time inseparable. In these cases, a particular spatial location cannot be designated, unambiguously, as belonging to either an on or off subregion. However, separate on and off subregions may be clearly distinguished in the joint space-time domain. These subregions are generally tilted along an oblique axis. 3. Our observations show that spatial and temporal aspects of receptive-field structure mature with clearly different time courses. By 4 wk postnatal, the spatial symmetry and periodicity of simple-cell receptive fields have reached maturity. The spatial extent (or size) of these receptive fields is adult-like by 8 wk postnatal. In contrast, the response latency and time duration of spatiotemporal receptive fields do not mature until well beyond 8 wk postnatal. 4. By applying Fourier analysis to spatiotemporal receptive-field profiles, we have examined the postnatal development of spatial and temporal selectivity in the frequency domain. By 8 wk postnatal, spatial frequency tuning has clearly reached maturity. On the contrary, temporal frequency selectivity remains markedly immature at 8 wk. We have also examined the joint distribution of optimal spatial and temporal frequencies. From 4 wk postnatal until 8 wk postnatal, the range of optimal spatial frequencies increases substantially, whereas the range of optimal temporal frequencies remains largely unchanged. From 8 wk postnatal until adulthood, there is a large increase in optimal temporal frequencies for cells tuned to low spatial frequencies. For cells tuned to high spatial frequencies, the distribution of optimal temporal frequencies does not change much beyond 8 wk postnatal.(ABSTRACT TRUNCATED AT 400 WORDS)


1989 ◽  
Vol 3 (4) ◽  
pp. 351-363 ◽  
Author(s):  
V. D. Glezer ◽  
V. V. Yakovlev ◽  
V. E. Gauzelman

AbstractThe number of subregions in the activity profiles of simple cells varies in different cells from 2–8; that is, the number of cycles in the weighting function varies from 1–4. The distribution of receptive-field (RF) sizes at eccentricities of 0-6 deg are clustered at half-octave intervals and form a discrete distribution with maxima at 0.62, 0.9, 1.24, 1.8, 2.48, and 3.4 deg. The spatial frequencies to which the cells are tuned are also clustered at half-octave intervals, forming a discrete distribution peaking at 0.45, 0.69, 0.9, 1.35, 1.88, 2.7, 3.8, and 5.6 cycles/deg. If we divide the RF sizes by the size of the period of the subregions, then the average indices of complexity (really existing) or the number of cycles in the weighting function form (after normalization) the sequences: 1, 1.41, 2.0, 2.9, 4.15.The relation between the bandwidth of the spatial-frequency characteristic and the optimal spatial frequency is in accordance with predictions of the Fourier hypothesis. The absolute bandwidth does not change with the number of cycles/module. This means that inside the module the absolute bandwidth does not change with the number of the harmonic. The results allow us to suggest the following. A module of the striate cortex, which is a group of cells with RFs of equal size projected onto the same area of central visual field, accounts for the Fourier description of the image. The basis functions of the module are composed of four harmonics only, irrespective of size and position of the module.Besides linear cells (sinusoidal and cosinusoidal elements), the module contains nonlinear cells, performing a nonlinear summation of the responses of sinusoidal and cosinusoidal elements. Such cells are characterized by an index of complexity which is more than the number of cycles in the weighting function and by marked overlap of ON and OFF zones. The analysis of organization suggests that the cells can measure the amplitude and phase of the stimulus.


1984 ◽  
Vol 52 (3) ◽  
pp. 538-552 ◽  
Author(s):  
K. R. Jones ◽  
R. E. Kalil ◽  
P. D. Spear

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)


1997 ◽  
Vol 78 (1) ◽  
pp. 366-382 ◽  
Author(s):  
Earl L. Smith ◽  
Yuzo Chino ◽  
Jinren Ni ◽  
Han Cheng

Smith, Earl L., III, Yuzo Chino, Jinren Ni, and Han Cheng. Binocular combination of contrast signals by striate cortical neurons in the monkey. J. Neurophysiol. 78: 366–382, 1997. With the use of microelectrode recording techniques, we investigated how the contrast signals from the two eyes are combined in individual cortical neurons in the striate cortex of anesthetized and paralyzed macaque monkeys. For a given neuron, the optimal spatial frequency, orientation, and direction of drift for sine wave grating stimuli were determined for each eye. The cell's disparity tuning characteristics were determined by measuring responses as a function of the relative interocular spatial phase of dichoptic stimuli that consisted of the optimal monocular gratings. Binocular contrast summation was then investigated by measuring contrast response functions for optimal dichoptic grating pairs that had left- to right-eye interocular contrast ratios that varied from 0.1 to 10. The goal was to determine the left- and right-eye contrast components required to produce a criterion threshold response. For all functional classes of cortical neurons and for both cooperative and antagonistic binocular interactions, there was a linear relationship between the left- and right-eye contrast components required to produce a threshold response. Thus, for example for cooperative binocular interactions, a reduction in contrast to one eye was counterbalanced by an equivalent increase in contrast to the other eye. These results showed that in simple cells and phase-specific complex cells, the contrast signals from the two eyes were linearly combined at the subunit level before nonlinear rectification. In non-phase-specific complex cells, the linear binocular convergence of contrast signals could have taken place either before or after the rectification process, but before spike generation. In addition, for simple cells, vector analysis of spatial summation showed that the inputs from the two eyes were also combined in a linear manner before nonlinear spike-generating mechanisms. Thus simple cells showed linear spatial summation not only within and between subregions in a given receptive field, but also between the left- and right-eye receptive fields. Overall, the results show that the effectiveness of a stimulus in producing a response reflects interocular differences in the relative balance of inputs to a given cell, however, the eye of origin of a light-evoked signal has no specific consequence.


2016 ◽  
Vol 6 (1) ◽  
Author(s):  
Zhen Ren ◽  
Jiawei Zhou ◽  
Zhimo Yao ◽  
Zhengchun Wang ◽  
Nini Yuan ◽  
...  

Abstract It is well known that, in humans, contrast sensitivity training at high spatial frequency (SF) not only leads to contrast sensitivity improvement, but also results in an improvement in visual acuity as assessed with gratings (direct effect) or letters (transfer effect). However, the underlying neural mechanisms of this high spatial frequency training improvement remain to be elucidated. In the present study, we examined four properties of neurons in primary visual cortex (area 17) of adult cats that exhibited significantly improved acuity after contrast sensitivity training with a high spatial frequency grating and those of untrained control cats. We found no difference in neuronal contrast sensitivity or tuning width (Width) between the trained and untrained cats. However, the trained cats showed a displacement of the cells’ optimal spatial frequency (OSF) to higher spatial frequencies as well as a larger neuronal signal-to-noise ratio (SNR). Furthermore, both the neuronal differences in OSF and SNR were significantly correlated with the improvement of acuity measured behaviorally. These results suggest that striate neurons might mediate the perceptual learning-induced improvement for high spatial frequency stimuli by an alteration in their spatial frequency representation and by an increased SNR.


1996 ◽  
Vol 75 (3) ◽  
pp. 1163-1176 ◽  
Author(s):  
P. Hammond ◽  
J. N. Kim

1. Single binocularly driven complex neurons in cat striate cortex were recorded extracellularly under nitrous oxide-oxygen-halothane anesthesia and muscle relaxant. Orientational/directional tuning was initially derived for each eye in turn, with sine wave gratings of optimal spatial frequency and velocity, while the other eye viewed a uniform field. 2. For the dominant eye, previously concealed suppression was revealed against elevated levels of firing induced with a conditioning grating, drifting continuously in the preferred direction, simultaneously presented to the nondominant eye. During steady-state binocular conditioning, orientational/directional tuning was reestablished for the dominant eye. In a subset of cells, tuning curves during conditioning were also derived for the reverse configuration, i.e., nondominant eye tuning, dominant eye conditioning: results were qualitatively identical to those for conditioning through the nondominant eye. 3. Neurons were initially segregated into five groups, according to the observed suppression profiles induced at nonoptimal orientations/directions during conditioning: Type 1, suppression centered on orthogonal directions; Type 2, suppression around null directions; Type 3, null suppression combined with orthogonal suppression; Type 4, lateral suppression, maximal for directions immediately flanking those inducing excitation; and Type 5, the residue of cells, totally lacking suppression or showing complex or variable suppression. 4. Sharpness of (excitatory) tuning was correlated with directionality and with class of suppression revealed during binocular conditioning. Direction-biased neurons were more sharply orientation tuned than direction-selective neurons; similarly, neurons exhibiting lateral or orthogonal suppression during conditioning were more sharply tuned than neurons with null suppression. 5. Application of suboptimal directions of conditioning weakened the induced suppression but altered none of its main characteristics. 6. The relationship between excitation, suppression, and spatial frequency was investigated by comparing tuning curves for the dominant eye at several spatial frequencies, without and during conditioning. End-stopped neurons preferred lower spatial frequencies and higher velocities of motion than non-end-stopped neurons. Confirming previous reports, suppression in some neurons was still present for spatial frequencies above the cutoff frequency for excitation, demonstrating the tendency for suppression to be more broadly spatial frequency tuned than excitation. 7. Scatterplots of strength of suppression, in directions orthogonal and opposite maximal excitation, partially segregated neurons of Types 1-3. Clearer segregation of Types 1-4 was obtained by curve-fitting to profiles of suppression, and correlating half-width of tuning for suppression with the angle between the directions of optimal suppression and optimal excitation in each neuron. 8. Two interpretations are advanced-the first, based on three discrete classes of inhibition, orthogonal, null and lateral; the second, based on only two classes, orthogonal and null/lateral--in which null and lateral suppression are manifestations of the same inhibitory mechanism operating, respectively, on broadly tuned direction-selective or on sharply tuned direction-biased neurons. Orthogonal suppression may be untuned for direction, whereas lateral and null suppression are broadly direction tuned. Within each class, suppression is more broadly spatial frequency tuned than excitation. 9. It is concluded that orientational/directional selectivity of complex cells at different spatial frequencies is determined by the balance between tuned excitation and varying combinations of relatively broadly distributed or untuned inhibition.


1999 ◽  
Vol 11 (5) ◽  
pp. 502-510 ◽  
Author(s):  
Heinz Schärli ◽  
Alison M. Harman ◽  
John H. Hogben

It is well known that a lesion in the optic radiation or striate cortex leads to blind visual regions in the retinotopically corresponding portion of the visual field. However, various studies show that some subjects still perceive certain stimuli even when presented in the “blind” visual field. Such subjects either perceive stimuli abnormally or only certain aspects of them (residual vision) or, in some cases, deny perception altogether even though visual performance can be shown to be above chance (blindsight). Research on monkeys has suggested a variety of parallel extrastriate visual pathways that could bypass the striate cortex and mediate residual vision or blindsight. In the present study, we investigated a subject with perimetrically blind visual areas caused by bilateral brain damage. Black and white stimuli were presented at many locations in the intact and affected areas of the visual field. The subject's task was to state, using confidence levels, whether the target stimulus was black or white. The results revealed an area in the “blind” visual field in which the subject perceived a light flash when the experimental black stimulus was presented. We hypothesize that a spared region in the visual cortex most likely accounts for these findings.


Perception ◽  
1996 ◽  
Vol 25 (5) ◽  
pp. 523-530 ◽  
Author(s):  
Jonathan S Pointer

Analysis of recently published human contrast-sensitivity data obtained along the cardinal and major oblique visual-field meridians of a single subject has demonstrated a consistently greater sensitivity at a given eccentricity to horizontally oriented as compared with obliquely oriented gratings. This difference was evident not only at foveal but also at several eccentric loci over a range of low to medium spatial frequencies. This observation is to be distinguished in extrafoveal fixation from the well-documented oblique effect, which describes the variation in sensitivity with orientation at a single visual-field locus. With periodic stimuli which were well localised in space and frequency, and had comparable spatial-summation properties, a spatial-frequency dependency of what could be termed the global oblique effect could be demonstrated along isoeccentric contours centred on the fovea (eccentricity 0 deg) out to an eccentricity of at least 40 deg.


Sign in / Sign up

Export Citation Format

Share Document