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At least 325 records · Page 18Linked to original sources

Visual persistence of stereoscopic stimuli: electric brain activity without perceptual correlate.

Dynamic random-dot stereograms (RDS) were used to study cortical neuronal mechanisms related to visual persistence in nine subjects. Electric brain potential components evoked by stereoscopic stimuli were compared to those evoked by conventional checkerboard stimuli with contrast borders. In a pattern-onset/offset presentation visual persistence thresholds were significantly lower for stereoscopic than for contrast stimuli: with temporally modulated patterns stereoscopic stimuli appeared to visually persist at much shorter interstimulus intervals than contrast stimuli. With stereoscopic stimuli all subjects reported not seeing changes of the RDS pattern, while the corresponding evoked potentials showed components related to the stimulus changes indicating a consistent discrepancy between psychophysical and electrophysiological data. The electrical brain activity was not caused by vergence eye movements elicited by the stereoscopic stimulus. In addition, for dynamic RDS stimuli a significant inverse linear relationship between temporal modulation frequency and evoked potential amplitude was found which was not observed with comparable contrast stimuli.

Adult↗

Electro-physiological investigation of edge-selective mechanisms of human vision.

This study investigates the spatial and temporal characteristics of human visual mechanisms that respond selectively to the polarity of edges. The technique was to record steady-state visual evoked-potentials (VEPs) while visually stimulating with a sawtooth waveform (a series of edges of the same polarity) periodically reversing in contrast (and hence edge-polarity) at a suitable frequency. To ensure that phase-locked VEPs resulted from polarity reversal (rather than local luminance modulation) the stimuli were randomly jittered to a new position between each contrast reversal. The jittered stimulus elicited strong and reliable second-harmonic modulation, usually about one-fifth the amplitude of standard VEPs under similar conditions. The amplitude and extrapolated thresholds of polarity-specific VEPs (relative to standard VEPs) did not vary with eccentricity (up to 10 degrees) or with stimulus orientation. The dependency on spatial frequency was similar to that of standard VEPs, but the polarity-specific VEPs tended to peak at lower temporal frequencies. Perhaps the clearest difference in the two types of VEPs was in the estimated response latency, about 140 msec for the polarity VEPs, compared with 90 msec for standard VEPs.

Contrast Sensitivity↗

The phase of PVEP in Maxwellian view: influence of contrast, spatial and temporal frequency.

The temporal phase of the pattern reversal VEP has been investigated using stimulation with laser interference fringes in Maxwellian view. VEP phase was almost constant as function of spatial frequency (2-30 c/deg, 6.5 r/sec, 51 subjects). The phase function however shows a small phase increase at low spatial frequencies consistent with the existence of multiple temporal mechanisms. Contrast variation yields a smaller phase increase with decreasing contrast than conventional stimulation. The phase is linear as function of reversal rate (2-31 r/sec) for low and high spatial frequencies. The indication of more than one temporal mechanism has also been found when the test field diameter was varied. With decreasing test field size the phase increases at 6.5 r/sec, but decreases at 18 r/sec (for 12 c/deg).

Adult↗

Electrophysiological correlates of texture segregation in the human visual evoked potential.

We investigated whether the visual evoked potential (VEP) reflects cortical processing associated with preattentive texture segregation. On a visual display unit we presented stimuli with various arrangements of oriented line segments that either led to the appearance of a "preattentive" checkerboard or did not. Two presentation modes were used (pattern onset at 1 Hz and rapid pattern change at 4.3 Hz), while luminance (57 cd/m2) and contrast (92%) of the line segments remained constant. VEPs were recorded in 7 human subjects. The VEP was analyzed as a linear combination of putative components, which are evoked by either local pattern, quasi-local orientation contrast or global preattentive structure. In the transient VEP, we found a negativity over the posterior pole at a latency between 161 and 225 msec (FWHM) in the linear combination designed to extract segregation-specific components. Peak amplitude reached 3.1 +/- 0.8 microV (mean +/- SEM) at 199 msec. This negative peak appeared only for textures containing orientation contrast. Steady-state analysis of the rapid presentation also revealed a significant component (P = 0.002) associated with texture segregation. These potentials either represent processing of orientation contrast or global processing of texture segregation. The results suggest that specific surface potentials, differing from cognitive potentials, can be derived which are associated with preattentive processing.

Adult↗

Stereopsis and binocularity in the squirrel monkey.

The squirrel monkey lacks anatomically demonstrable ocular dominance columns, and physiologically it has an ocular dominance distribution in V1 that is very different from that of macaques, with far fewer cells that strongly favor one eye over the other. We tested an alert squirrel monkey for physiological responses to stereoscopic stimuli by measuring evoked potentials in response to cytclopean patterns generated in dynamic random-dot stereograms. The monkey showed evoked responses both to changes in disparity and to shifts between correlation and uncorrelation between the two eyes. This result strongly suggests that the squirrel monkey can detect stereoscopic depth, which in turn casts some doubt on the assumption that ocular dominance columns bear an important relation to stereopsis.

Animals↗

A pupillometric correlate of scotopic visual acuity.

While not easily fit into the classic descriptions of the pupillary light reflex, previous studies reported that changes in the spatial composition of the retinal image can evoke a pupillary response. The present study extends this observation by showing that the pupil constricts in response to scotopic as well as photopic spatial patterns. Moreover, the amplitude of the scotopic response decreases with increasing spatial frequencies suggesting a pupillary spatial acuity of about 3 c/deg. The scotopic pupil acuity is similar to the scotopic perceptual visual acuity measured in the same observers.

Adult↗

Spatial-frequency specific contrast gain and flicker masking of human transient VEP.

We studied the effects of grating contrast and luminance-flicker masking on the early waves of human visually evoked potentials (VEPs) recorded at the onset-offset of sinusoidal gratings of varying spatial frequencies (SFs). At high SFs, the response waveform was simple and VEP was dominated by a negative wave (N110). At low SFs, several positive-negative deflections were recorded, the earliest dominating wave being positive (P90). The amplitude of P90 was saturated at a contrast of about 0.1 and it was attenuated by flicker masking. Masking involved to a lesser extent the waves following P90. It was weaker at the flicker frequency of 5 Hz than at 10 and 20 Hz. No flicker masking was found at SFs higher than 2-4 c/deg. At medium and high SFs, VEPs were obtained at higher contrast levels. No saturation (max contrast tested 0.5) and no flicker masking of N110 were observed. These results suggest that the early VEP components recorded at low and high SFs are related to different types of neuronal activity. Correlation between VEP properties and properties of magnocellular and parvocellular pathways is considered with an emphasis on recent morphological data about the human retina.

Adolescent↗

Visual evoked potentials following abrupt contrast changes.

The timing of visual evoked potential (VEP) amplitude and phase changes following abrupt increases or decreases in contrast was examined. Gratings (1 c/deg) were presented at a low contrast for 8 sec, increased to a higher contrast for 8 sec, and then decreased to the initial lower contrast for another 8 sec. Second harmonic VEP amplitude and phase were recorded continuously and averaged in 1 sec epochs. Both amplitude and phase exhibited delays in reaching a stable level following the contrast change. For amplitude, the length of the delay was dependent on the magnitude and direction of the contrast step and on the spatial frequency of the stimulus. Time constants for the change in amplitude following step increases in contrast ranged from 0.2 sec for a 12% contrast step to 1.34 sec for a 37% contrast step. The timing of phase changes, however, was independent of the size of the contrast increases (tau = 0.7 sec). For step decreases in contrast, both amplitude and phase were relatively independent of the size of the change (tau = approx. 0.9 sec for amplitude and tau = 0.15 sec for phase). Amplitude time constants also increased with increasing spatial frequency (tau = 1.2 sec for 1 c/deg, tau = 1.6 sec for 4 c/deg and tau = 2.3 sec for 8 c/deg); phase time constants, however, did not change as a function of spatial frequency (tau = 0.7 for all spatial frequencies). These findings demonstrate that a unitary process may not always be tapped by signal averaging techniques. Additionally, swept stimulus VEP techniques may produce considerable errors in threshold estimation depending on the stimulus spatial frequency and on the slope and direction of the contrast change.

Contrast Sensitivity↗

Differences between stereopsis, interocular correlation and binocularity.

In normal human subjects, evoked potentials in response to depth reversing two-color dynamic random-dot stereograms disappeared or were greatly reduced at equiluminance, whereas responses to shifts between patterns that were correlated and anticorrelated (for the two eyes) were, for most subjects, actually larger at equiluminance than at non-equiluminance. Responses were only slightly diminished at equiluminance to similar texture-shifting patterns that were identical to the two eyes. These results suggest that a significant fraction of cells with input from both eyes can respond to correlation/anticorrelation shifts, yet are not involved in stereopsis. Also, binocular rivalry may gate the responses of these binocular-nonstereoscopic units.

Depth Perception↗

Linear and nonlinear contributions to step responses in cat retinal ganglion cells.

We measured excitatory and inhibitory step responses of cat retinal ganglion cells to square wave contrast reversal of stationary sinusoidal gratings. In most Y-cells the initial increase in firing rate (early peak) of the excitatory responses was followed by a distinct second increase in firing rate (late peak). Analysis of the spatial frequency and spatial phase dependence of the two peaks indicated that the early peak appears to be produced by the spatially linear center mechanism, while the late peak appears to be produced by the rectifying subunits described by Hochstein and Shapley (1976) Journal of Physiology, London, 262, 237-264, 265-284. These results indicate that the presence of two peaks in ganglion cell step responses is the result of two excitatory inputs with different time courses, and that inhibitory inputs are not required to explain the appearance of these responses.

Action Potentials↗

Development of the temporal properties of visual evoked potentials to luminance and colour contrast in infants.

We have studied the development of the temporal characteristics of the pattern visual evoked potentials (P-VEPs) in response to contrast reversal of patterns of low spatial frequency (0.1 c/deg) of either pure luminance contrast (yellow-black plaid patterns) or pure colour contrast (equiluminant red-green plaid patterns) in 15 infants between 6 and 30 weeks of age. High contrast patterns were modulated temporally either sinusoidally at various temporal frequencies to elicit steady-state responses, or abruptly at a low temporal frequency to elicit transient responses. Analysis of both the transient and steady-state responses suggests the existence of three different mechanisms contributing to the infant and adult P-VEP responses at low, medium and high temporal frequencies. The responses at the three different temporal frequency ranges have different time constants, and develop at different rates. The low frequency response predominates at 8 weeks, where it spans the range 1-6 Hz with an apparent latency of about 230 msec, for both colour and luminance stimulation. This response increases in bandwidth and decreases in latency progressively with age, at a similar rate for luminance and colour contrast, up to 14 weeks. After 14 weeks, the luminance response undergoes major changes, with the emergence of a new response with a shorter latency (about 100 msec) and a peak activity near 10 Hz. This mid-frequency response matures further with age, until it dominates the whole response of the adult P-VEP to luminance contrast. It also makes a contribution to the chromatic response at frequencies above 10 Hz, generating the characteristic double-peaked amplitude response in adults. However, its contribution is very limited below 10 Hz, where the response latency is 140 msec in adults, as it was at 14 weeks of age. A third component is evident at very high temporal frequencies of the luminance response as early as 6 weeks, extending up to 15 Hz in 8-week-olds and up to 25 Hz for older infants. It remains apparent up to 18 weeks, thereafter being swamped by the major mid-frequency response. The apparent latency of response over this frequency range is about 70 msec at all ages. The development of transient P-VEPs paralleled that of the steady-state P-VEPs. At all ages there was an early negative component (N70) at about 70 msec, corresponding to the fast steady-state response at high frequencies for luminance contrast. Before 14 weeks, the luminance and chromatic transient response had the same morphology, with a single major peak of similar latency to the apparent latency of the low temporal frequency response. After this age, the morphology of the luminance response changed, particularly in the first 100 msec, consistent with the emergence of the mid-frequency response. We discuss whether the high-frequency component may represent pre- or early post-synaptic cortical activity, already mature by 8 weeks, and how the different maturation rates of the mid and high-frequency components may reflect different intra-cortical circuitry for colour and luminance.

Adult↗

Direct and transcallosal contribution to the cortical visual evoked response in rats.

The averaged visually evoked cortical potential (VECP) in response to contrast reversal of a grating was measured on striate cortex over a range of spatial frequencies and contrasts. The response to binocular or monocular stimulation was almost abolished by unilateral section of the optic tract on the side of the recording, indicating that the transcallosal pathway makes little contribution to the VECP. Additional section of the corpus callosum, and application of spreading depression to the normal hemisphere shows that the small response following tract section was transcallosal. It was confined to stimuli of low spatial frequencies and high contrast.

Animals↗

The effect of eccentricity and colour on negativity in pattern onset visual evoked potentials.

The effects of stimulus size, eccentricity and colour on the amplitudes of N100 and N130 were investigated in pattern onset VEPs. For black-and-white pattern stimulation, the first set of stimuli was derived from a full dartboard pattern. Central stimulation of various extents was produced by patterns with reduced number of outer rings and for eccentric stimuli a number of central rings were removed from the full pattern. It was found that amplitude of N100 was maximal in VEPs to central stimuli and that it was greatly reduced when eccentric stimulation was applied. The amplitude of N130 showed no significant change in relation to the type of stimulus. When checkerboard stimuli of identical configuration were used for black-and-white pattern stimulation instead of dartboards, systematic changes in peak latencies of N100 were observed in relation to check size. In VEPs to centrally presented small checks the emergence of an early negative peak preceding N100 was recorded at 75 msec. In VEPs to coarse checkerboards presented centrally N100 was often observed with a delayed peak latency of 110 msec. Changes in N130 were not regular when checkerboards with different check sizes were presented centrally. For eccentric checkerboard stimulation, both negative peaks N100 and N130 were revealed. Their peak latencies were similar to those observed in the case of dartboard paracentral stimulation. In VEPs to patterns projected through red or blue filters, regular changes were observed in both negative peaks. Introduction of the red filter led to enhancement of the N100 amplitude in VEPs to dartboard and to checkerboards with fine checks, but it caused no effect on N100 in the VEPs to coarse checkerboards. Introduction of the blue filter led to a decrease in the N100 amplitude in VEPs to dartboard and fine checkerboards and to a slight increase of N100 in VEPs to coarse checkerboards. Changes in N130 were observed only when the blue filter was introduced and they corresponded to those which take place when the level of illumination changes from photopic to mesopic.

Color Perception↗

Stationary pattern adaptation and the early components in human visual evoked potentials.

Pattern-onset visual evoked potentials were elicited from humans by sinusoidal gratings of 0.5, 1, 2 and 4 cpd (cycles/degree) following adaptation to a blank field or one of the gratings. The wave forms recorded after blank field adaptation showed an early positive component, P0, which decreased in amplitude with spatial frequency, whereas the immediately succeeding negative component, N1, increased in amplitude with spatial frequency. P0 and N1 components of comparable size were recorded at 1 cpd. Stationary pattern adaptation to a grating of the same spatial frequency as the test grating significantly reduced N1 amplitude at 4, 2 and 1 cpd. The N1 component elicited at 4 cpd was attenuated in log-linear fashion as the spatial frequency of the adaptation grating increased. P0, on the other hand, was unaffected by stationary pattern adaptation at all combinations of test and adapting spatial frequencies, although P0 amplitude is known to be attenuated by adaptation to a drifting grating. Since N1, but not P0, was significantly attenuated following adaptation and testing at 1 cpd, it was concluded that the neurons generating these components are functionally distinct. The use of a common adaptation grating discounted the possibility that N1, but not P0, was affected due to a difference in the rates of retinal image modulation caused by eye movements made while viewing adaptation gratings of different spatial frequencies. The neurons generating N1 were adapted at a lower rate of retinal image modulation than that apparently required for adaptation of the neurons generating P0, which suggests a difference between these neurons in the rate of stimulus modulation necessary for activation.

Adaptation, Ocular↗

Comparison of the pattern reversal visual evoked potential mediated by separate cone systems.

With the purpose of recording responses mediated by the 3 cone systems visual evoked potentials (VEPs) were elicited by the reversal of monochromatic checkerboards superimposed upon strong monochromatic backgrounds (yellow, purple and blue-green). The sensitivity to light of various wave lengths were measured as the reciprocal of the intensity necessary to elicit a VEP amplitude of 3 microV. The spectral sensitivity curves based on this VEP amplitude criterion in the presence of blue-green, purple and yellow adaptation showed peak sensitivities in the red, the green and the blue part of the spectrum, respectively. This indicates that the responses reflect separate modulation of the 3 different cone mechanisms. The potentials obtained with yellow adaptation differed from those obtained with purple and blue-green adaptation. The amplitude versus log intensity function was flatter and the latency of the major positive peak was increased by 20-25 msec. Repeated examinations of 4 subjects suggest that the method yields reliable latency measurements of responses mediated by separate cone mechanisms.

Adult↗

Assessment of the relationship of cerebral hemisphere arousal asymmetry to perceptual asymmetry.

This study examined the hypothesis that characteristic individual differences in cerebral hemisphere arousal asymmetry are related to individual differences in perceptual asymmetry observed in verbally based visual half-field tasks. The study used electrophysiological measures of arousal asymmetry rather than behaviorally derived measures (Levy, Heller, Banich, & Burton, 1983). Measures of alpha asymmetry were obtained from 20 right-handed males during a baseline relaxation condition and during a visual half-field version of the lexical decision task. Reaction time measures of perceptual asymmetry were obtained during this task. The results indicated that a basal arousal asymmetry measured at the temporal recording location during the baseline condition was significantly related to individual perceptual asymmetry during the subsequent lexical decision task. This basal arousal asymmetry was relatively stable across different task conditions. A task-related arousal asymmetry measured at the parietal location during the lexical decision task also made a significant contribution in predicting individual perceptual asymmetry. These two measures of individual arousal asymmetry were able to predict 50% of the variance in perceptual asymmetry. The implications of the results for explaining more wide-ranging individual differences in behavioral style and personality are discussed.

Adult↗