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PubMed1977

Perception of wholes and of their component parts: some configural superiority effects.

Theories of visual pattern recognition frequently assume that processing begins with an analysis of the pattern into component parts, which are often assumed to be line segments of particular orientations, lengths, positions, and curvatures. The present experiments measured discriminability of these simple parts when presented either in isolation or within configural contexts that provided no formal information useful for the discrimination. Certain contexts either impaired or did not affect performance. Other contexts were found, however, which dramatically improved discriminability. Thus, two patterns which differed only in a single part could be discriminated from each other more quickly than could their distinguishing parts shown in isolation. Further experiments suggest that this "configural superiority" effect influences perceptual components of processing rather than memorial components. The mechanism underlying configural superiority appears to be the detection of novel and distinguishing features, such as corners and intersections, which emerge when parts are placed in close proximity to each other. The outlines of a model for preattentive feature discrimination are presented.

Adult↗
PubMed1985

Non-linearity of visual evoked potentials in cerveau isolé and midpontine pretrigeminal cats.

Characteristics of the visual evoked responses to the flickering flash stimulation were studied in the cerveau isolé and midpontine pretrigeminal cats. The flash stimulation frequency was changed stepwise between 1 and 30 Hz in increasing and decreasing order. In all cases of both preparations, with drawing of fixed sweep speed of 200 msec in whole length, P1 and N1 latencies in the successive response slightly prolonged progressively 1 to about 20 Hz and thereafter shortened about 20-30 Hz stimulus frequencies in the course of the increasing phase, and vice versa in the course of the decreasing phase. Moreover, no difference in each latency (P1, N1, P2, N2) was found at the same stimulus frequency during increasing and decreasing phases. In the amplitude taken from the P1-N1 component, the peak was found in 5-9 Hz frequency bands. This peak was higher during the decreasing phase than during the increasing phase, which indicated a hysteresis phenomenon. A peak of power for the 1st harmonics was found at 3-6 Hz driving frequency bands, and that of the 2nd harmonics at 6-10 Hz. In the state without flash stimulus, no peaks or valleys in the power spectrum were found in specific frequencies, for example 3-10 Hz. The peak in the amplitude and that in the power spectrum at 3-10 Hz stimulus frequency bands suggested an entrainment phenomenon induced by forced oscillation. The phenomena of entrainment and hysteresis suggest the existence of a non-linear structure in the oscillation generating systems of visual evoked response.

Animals↗
PubMed1992

Wulst efferents in the little owl Athene noctua: an investigation of projections to the optic tectum.

The efferent projections from the Wulst were studied in the little owl, Athene noctua, using anterograde migration of wheat-germ-agglutinin conjugated horseradish peroxidase (WGA-HRP). Wulst projections were distributed to telencephalic, diencephalic and mesencephalic targets in a general pattern similar to that previously described in other avian species. Our results on the organization of the Wulst-optic tectum pathway in the little owl reveal well defined and laminarly arranged terminal projections into the superficial tectal layers, with a distribution suggestive of topographical relationships between neurons of origin in the Wulst and termination fields in the optic tectum. In contrast to lateral-eyed birds, the little owl possesses conspicuous contralateral projections to the optic tectum. Ipsilateral and contralateral efferents are restricted to different tectal regions, i.e. ipsilateral projections to the caudo-dorsal and contralateral projections to the rostro-ventral optic tectum. In addition, the anterior and posterior Wulst differentially contribute to the ipsilateral and contralateral projections to the optic tectum. This differential organization of Wulst efferents, as well as the presence of substantial contralateral projections, might be related to the high degree of binocular overlap typical of frontal-eyed birds. At a functional level, electric potentials recorded in the optic tectum and evoked by visual stimulation showed that information from one eye can reach the ipsilateral optic tectum. After Wulst ablation, the amplitude of these potentials was significantly reduced, indicating that Wulst efferents may influence visually-evoked activity in the optic tectum.

Animals↗
PubMed1991

[Contrast transfer function of the visual system].

Visually evoked potentials were used to determine the spatial contrast response function of the visual system and the visual acuity of the pigeon. The spatial contrast response describes the relationship between the contrast in a pattern of vertical stripes, whose luminance is a function of position, and the amplitude of the visually evoked response at various spatial frequencies for a given temporal frequency (pattern reversal frequency); it indicates how particular spatial frequencies are attenuated in the visual system. The visually evoked responses were recorded using monopolar stainless steel electrodes inserted into the stratum griseum superficiale of the optic tectum; the depth of penetration was determined on the basis of a stereotactic atlas. The stimulus patterns were generated on a video monitor placed 75 cm in front of the animal's eye perpendicular to the optic axis. The spatial contrast response function measured at 10% contrast and 0.5 Hz reversal frequency shows a peak at a spatial frequency of 0.5 c/deg, corresponding to 1 degree of visual angle, and decreases progressively at higher spatial frequencies. The high-frequency limit (cut-off frequency) for resolution of sinusoidal gratings, estimated from the contrast response function, is 15.5 c/deg, corresponding to a visual acuity of 1.9 min of arc.

Animals↗
PubMed1992

The topographic distribution of the magnetic P100M to full- and half-field stimulation.

Visual evoked magnetic responses were recorded to full-field and left and right half-field stimulation with three check sizes (70', 34' and 22') in five normal subjects. Recordings were made sequentially on a 20-position grid (4 x 5) based on the inion, by means of a single-channel direct current-Superconducting Quantum Interference Device second-order gradiometer. The topographic maps were consistent on the same subjects recorded 2 months apart. The half-field responses produced the strongest signals in the contralateral hemisphere and were consistent with the cruciform model of the calcarine fissure. Right half fields produced upper-left-quadrant outgoing fields and lower-left-quadrant ingoing fields, while the left half field produced the opposite response. The topographic maps also varied with check size, with the larger checks producing positive or negative maximum position more anteriorly than small checks. In addition, with large checks the full-field responses could be explained as the summation of the two half fields, whereas full-field responses to smaller checks were more unpredictable and may be due to sources located at the occipital pole or lateral surface. In addition, dipole sources were located as appropriate with the use of inverse problem solutions. Topographic data will be vital to the clinical use of the visual evoked field but, in addition, provides complementary information to visual evoked potentials, allowing detailed studies of the visual cortex.

Adult↗
PubMed1991

Spatial frequency of the human short-wavelength-sensitive (blue) cone mechanism. Psychophysical studies and pattern-reversal visual evoked potentials.

The interactions of spatial and chromatic processing of the short-wavelength-sensitive cone mechanism were studied in humans with patterned (checkerboard) stimuli of various spatial frequency (10, 22, 44, and 85 min of are respectively), under steady exposure to yellow light (575 nm, 390 cd/m2). Psychophysical studies and pattern-reversal visual evoked potentials were employed. Parameters of the transient pattern-reversal visual evoked potentials (pattern reversal rate of 2.4 s-1) especially observed were the latencies of P2 (P100) and N3 and the amplitude of P2-N3. It was only with the largest applicable check size (85 min of arc) that both the psychophysical studies and visual evoked potentials could succeed in satisfactorily isolating the short-wavelength-sensitive cone mechanism. Pattern-reversal visual evoked potential latencies are recommended in the evaluation of this cone mechanism because of their smaller variance and higher selectivity in isolating the short-wavelength-sensitive cone mechanism than the amplitude. The peak sensitivity of this cone mechanism was shown to be about 449 nm at the corneal level. The short-wavelength sensitive cone mechanism represented the characteristics of low spatial resolution and long latencies of the pattern-reversal visual evoked potentials.

Adult↗
PubMed1991

Visual evoked potential responses of the anesthetized cat to contrast modulation of grating patterns.

Contrast modulation affords independent control of static contrast (C) and changes in contrast (delta C). We found that in anesthetized, paralyzed cats, the visual evoked potential (VEP) was dependent only on magnitude of delta C at each pattern transition, and was independent of the starting or ending contrast level. Increasing modulation frequency to above 2 Hz reduced the VEP monotonically, implying that the time constant for differentiation by the VEP is of the order of 250 msec. The essentially perfect a.c. coupling suppresses standing contrast completely, permitting the full dynamic range of the VEP response system to be used for detection of contrast increments (which results in a decreasing Weber fraction). The difference between our results and those of behavioral studies using contrast modulation can be explained by eye movements present in the behavioral studies which refresh the retinal image of the static contrast in a way uncorrelated to temporal modulation of the stimulus, thus introducing a masking effect.

Anesthesia, General↗
PubMed1992

Analysis of striate activity underlying the pattern onset EP of children.

The checkerboard onset Evoked Potential (EP) does not obtain its adult form before puberty. To determine the site of origin of these processes we studied the origin of the checkerboard onset EP in a group of 10 children between the ages of 6 and 16 years. Since the development of the waveform of the pattern onset EP varies with check size we also studied the dependence of these EPs on check size. The child checkerboard onset EPs described in this paper are dominated by a single source. Following an equivalent dipole source localization approach, the position, orientation and variation in strength of the equivalent dipole is estimated. The position and orientation of this dipole indicates an origin in the primary visual cortex (area 17). The variation in strength of the dipole changes from a single positive deflection, specific for children of 8 years and younger, into a negative-positive complex for the children studied between the age of 9 and 16 years. These changes in waveform must be due to changes in the activity pattern of the striate cortex.

Adolescent↗
PubMed1986

Methods for the identification of evoked response components in the frequency and combined time/frequency domains.

Two prominent frequency components designated f1 and f2 have been identified in the visual evoked response to the transient presentation of sinusoidal luminance gratings in the range of 0.5-8 c/deg. The components occur at temporal frequencies below the alpha band, with the f1 frequency being roughly half that of the f2 frequency. The f1 component is largest at low spatial frequencies with f2 becoming progressively dominant as spatial frequency is increased. The frequency and amplitude of f1 and f2 change substantially over the time course of the response. This has been studied by calculating the temporal frequency spectrum of the transient evoked potential over successive short-time epochs running through the response. Using this technique, the response is shown to consist of narrow-band frequency peaks or 'formants' emerging at different times after stimulus onset. These formants occur at frequencies other than those of the spontaneous EEG and undergo changes in frequency and amplitude over the time course of the response. Two spectrum analysis techniques were employed: the Discrete Fourier Transform and Linear Predictive Coding. Frequency components were successfully identified in single-trial responses using the LPC technique.

Electroencephalography↗
PubMedDate not supplied

Neuronal generators of the visual evoked potentials: intracerebral recording in awake humans.

Flash and pattern reversal visual evoked potentials were recorded in awake patients undergoing stereotactic procedures for severe dyskinetic disorders resistant to medical treatment. The nucleus ventralis lateralis thalami was reached via an occipital approach. VEPs were recorded on the scalp at the entrance of the intracerebral electrode, and serially from sites at different depths. A polarity reversal of the surface recorded wave form took place as the intracerebral electrode was advanced beneath the surface cortical layers. As concerns F-VEPs, most of the scalp activity mirrored the potentials recorded down to the depth of 70-65 mm from the thalamus. The largest amplitude of intracerebral F-VEPs was obtained from recording sites at 50-70 mm from the thalamus, i.e., in the depth of the calcarine fissure. A negative wave, peaking around 47-50 msec, became evident in recording sites at 30-40 mm from the thalamus but vanished as the electrode was advanced farther. In only one patient could we record a small negative wave, peaking at 33 msec, in the vicinity of the corpus geniculatum externum. Furthermore, the oscillatory activity recorded from the scalp appeared to be generated in the cortical layers. PR-VEPs also underwent polarity reversal as the electrode traversed the cortex. PR-VEPs disappeared more superficially than F-VEPs. No PR-evoked activity could be recorded in the vicinity of the corpus geniculatum externum. We conclude that slow and fast components of VEPs recorded from the scalp are entirely generated in cortical layers.

Brain Mapping↗
PubMedDate not supplied

The influence of pattern size on amplitude, latency and wave form of retinal and cortical potentials elicited by checkerboard pattern reversal and stimulus onset-offset.

Transient pattern electroretinograms (PERGs) and visual evoked potentials (VEPs) were recorded with checkerboard pattern reversal and equiluminance stimulus onset-offset, elicited by a high quality moving mirror stimulator. Different sized checkerboard patterns (0.35-4.2 c/deg) were used as stimulus patterns. The wave forms of the equiluminance stimulus onset responses were similar to ERGs evoked with luminance decrease and the stimulus offset PERGs were like ERGs elicited by luminance increase. The PERG c wave and the VEP showed spatial frequency tuning with pattern reversal and stimulus offset. Spatial frequency tuning was not detectable with PERG a and b waves. Pattern reversal and stimulus onset evoked PERGs had no major spectral components above 40 Hz; stimulus offset evoked PERGs contained components up to 55.3 Hz. Retino-cortical time--measured as a latency difference of the PERG b wave to VEP P100--was identical with pattern reversal and stimulus onset and about 12 msec longer with stimulus offset. Our results suggest that the 3 stimulation modes, reversal, onset and offset induce different types of processing at the retinal and cortical levels. PERG a and b waves to our high luminance/contrast stimuli contain no pattern specific information and the c waves are the sum of luminance and pattern specific responses.

Cerebral Cortex↗
PubMed1992

Alterations in rat flash and pattern reversal evoked potentials after acute or repeated administration of carbon disulfide (CS2).

Because solvents may selectively alter portions of visual evoked potentials, we examined the effects of carbon disulfide (CS2) on flash (FEPs) and pattern reversal (PREPs) evoked potentials. Long-Evans rats were administered ip carbon disulfide either acutely or for 30 days. FEPs or PREPs were recorded prior to and 1, 2, 4, 8, or 24 hr after a single dose of CS2 (0, 100, 200, 400, or 500 mg/kg). Flash evoked potentials were also recorded 1, 2, 6, and 24 hr after the last of 30 doses of 200 mg CS2/kg/day. Acute exposure to CS2 consistently decreased the amplitude of FEP peak N160 at 1 hr, depressed peak N30 amplitude over 2-4 hr, and increased the latency of peaks P21, N30, P46, N56, and N160 for up to 4 hr after treatment. Carbon disulfide decreased the amplitude of PREP peaks P65, N83, P88, and N122 4 hr after treatment. Colonic temperature was depressed up to 8 hr after treatment. Administration of 200 mg CS2/kg/day decreased the amplitude of FEP peak N30 and increased the latencies of peaks P21, N30, P46, N56, and N160 up to 24 hr after the last dose. The differential effects of CS2 on portions of FEPs indicate that FEP peaks can be independently modulated. Changes in PREPs were temporally correlated with alterations in early FEP peaks, but FEP peak N160 was depressed at an earlier time point. Repeated CS2 exposure affected FEPs at lower doses and for a longer time than an acute exposure, similar to the reported greater severity of neurological disturbances following repeated CS2 exposures in humans.

Animals↗
PubMed1992

A developmental event-related potential study of picture matching in children, adolescents, and young adults: a replication and extension.

Event-related potentials were recorded in a developmental study of picture matching using an adaptation of Posner's (1978) letter-matching tasks. Subjects ranging in age from 6-39 were asked to decide whether two line drawings, presented sequentially, were the same or different on the basis of physical (physical identity), nominal (name identity), or categorical (category identity) criteria. The amplitude of a negativity at 400 ms (Neg400) increased as the number of dimensions on which the two line drawings differed increased. This effect held for all age groups, and was interpreted as reflecting the degree of semantic and/or physical relationship between the two pictures. However, one finding for Neg400 did suggest a qualitative difference in processing mode between the younger and older subjects. Both Neg400 and P3b latencies showed highly significant linear age trends, decreasing with increasing age. These age-related changes were interpreted as demonstrating quantitative speed of processing differences among age groups. The latencies of both Neg400 and P3b increased as the matching criteria became more complex. Moreover, P3b latency increased as the number of dimensions on which the two pictures differed increased, and this did not interact with age. Although both Neg400 and P3b showed age-related changes in scalp distribution, the fact that each was related to the experimental variables in similar fashion in all age groups suggested that they were homologous components across the age range studied. Taken as a whole, the data support continuity of information processing during these tasks across a wide age range.

Adolescent↗
PubMed1989

Pattern-reversal visual evoked potentials in normal 7- to 15-year-old twins: a correlation analysis.

Pattern-reversal visual evoked potentials (PRVEPs) were tested in 11 sets of monozygotic (MZ) twins and 22 sets of dizygotic (DZ) twins matched on age, sex and educational level. They ranged in age from 7 to 15 years. The PRVEPs of MZ twins exhibited a significantly greater degree of similarity than those of DZ twins. The peak latencies and amplitudes of PRVEP components obtained from MZ twin pairs were significantly correlated. The correlation coefficients for the peak latencies of the P2 (or P100) component were the only ones to differ significantly between the DZ twins of the same sex and DZ twins of opposite sexes. These coefficients, obtained using PRVEPs, were much greater than those obtained with flash visual evoked potentials.

Adolescent↗
PubMed1988

Visual evoked potentials in elderly patients with primary or multi-infarct dementia.

Flash and pattern-reversal visual evoked potentials (VEP) were recorded in 35 elderly patients with dementia, and 19 controls of equivalent age. Dementia produced a slowing of the major positive (P2) component of the flash VEP but did not affect the latency of the flash P1 component or the P100 pattern-reversal component. This unusual type of abnormality was found in both primary and multi-infarct types of dementia, and has previously been found in primary presenile dementia. The results show that the VEP can be used for the diagnosis of multi-infarct, and primary presenile and senile dementias.

Aged↗
PubMed1991

Quantitative analysis of the cross-correlation between pattern ERG and pattern VEP.

The cross-correlation between PVEPs and PERG was investigated. (1) There were high correlations between PVEPs recorded from the inion and those from points Oz, Pz, Cz, and Fz in the range of 75-150 msec following pattern visual stimulation to the eyes although no correlation was found in the range 0-75 msec. (2) PVEPs recorded from the inion highly correlated with PERG in the 75-150 msec range but not in the 0-75 msec range. It suggests that the late negative component included in the PERG reflected the electrotonically spread at the eye level of PVEP. (3) Intra-individual reproducibility was studied. PVEPs showed a high reproducibility in the 75-150 msec range, but not in the 0-75 msec range. The reproducibility of PERG was high in the 0-75 msec range but also in the 75-150 msec range, where PERG reflected PVEPs. These results suggest that the early positive component of PERG was specific to the cell activities in the retina to the pattern visual stimulus, and had an origin different from the brain activity for PVEPs.

Adult↗