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Biomedical subjects

E W Yund

Publications and source records attributed to E W Yund.

At least 19 recordsLinked to original sources

Visual detectability gradients: effect of illiteracy.

When subjects are required to detect a target pattern presented simultaneously with a number of similar non-target patterns in a brief exposure, marked differences of target detectability are observed as a function of the spatial location of the target (Efron, Yund, & Nichols, 1987, 1990a, b, c; Yund, Efron & Nichols, 1990a, b, c). These differences in detectability as a function of retinal locus, referred to collectively as a "detectability gradient," have been attributed to a central serial processing mechanism, which scans the decaying neural representation of the image. There also is evidence suggesting that, at least in some circumstances, this gradient may be influenced by the direction in which subjects normally read (Heron, 1957; Mishkin & Forgays, 1952; Efron et al., 1987). The object of the present experiment was to determine whether the detectability gradient obtained with the non-linguistic stimuli used in our previous experiments would differ as a function of previous reading experience. The experiment was performed on a group of 60 illiterate subjects and on a socioeconomic-matched group of 60 literate subjects. While the overall accuracy of target detection was identical in the two groups, there were significant differences between the detectability gradients of the literate and illiterate subjects. The nature of these differences indicates that reading, or learning to read, causes the scanning mechanisms of literate subjects to adopt more consistent scan paths, from subject to subject, than they would have adopted without this reading experience.

Adult

Visual detectability gradients: effect of high-speed visual experience.

The detectability of a target pattern presented briefly with a number of similar nontarget patterns varies as a function of the spatial location of the target. Previous work attributes these detectability gradients to a visual search process--a non-eye movement serial scan--that examines a decaying neural representation of the image. (Heron, 1957; Efron, Yund, & Nichols, 1987, 1990a,b,c; Yund, Efron, & Nichols, 1990a,b,c). The results reported in the companion paper (Ostrosky-Solis, Efron, & Yund, 1991) indicated that literacy did not affect overall performance levels but did influence scanning behavior: "...reading, or learning to read, caused the scanning mechanisms of literate subjects to adopt more consistent scan paths, from subject to subject, than they would have adopted without this reading experience." The purpose of the present experiment was to determine the effect on this scanning mechanism, if any, of an entirely different type of visual experience--the high-speed visual processing required of tennis players. Unlike reading which requires the linguistic interpretation of a highly structured visual input, tennis skill requires rapid target detection and tracking in three-dimensional visual space as well as large scale visual-motor coordination. As in the previous experiments, subjects were required to detect a vertical stripe pattern among a number of similar non-target patterns. The experiment was performed on a group of 52 tennis players and on an age- and sex-matched group of 52 non-tennis players. The overall accuracy of target detection was greater among the tennis players than among the non-tennis players and, of more interest, there was a significant difference in the detectability gradients. The detection advantage of the tennis group seemed to reach its maximum in the first half of the scan and then to deteriorate as the scan proceeded. These results indicate that visual experience other than reading can affect the habitual activity of the scanning mechanism.

Adult

Detectability gradients as a function of target location.

We examined the ability to detect a specified visual pattern (a target) in a randomly selected location when it was briefly presented with 11 other spatially distributed nontarget patterns and also when it was presented by itself for the same duration (50 msec) on a background of visual noise. Two experiments were designed to measure target detectability as a function of its location in the visual field where all possible target locations were equidistant from the fovea. A right visual field detection superiority was obtained in both experiments. In addition, highly significant detectability differences were observed within the right and left visual fields in both experiments. The origin of these detectability differences are interpreted in terms of parallel and serial processing mechanisms.

Adult

Serial processing of visual spatial patterns in a search paradigm.

Previous experiments in this laboratory employing a search paradigm have found highly significant differences in the detectability of a briefly exposed target pattern as a function of the spatial location of the target when it is presented simultaneously with a number of discriminably different nontarget patterns. These detectability differences, at loci equidistant from the fovea, could not be accounted for by any known variation in retinal spatial resolution or by differential lateral masking effects of the target by nearby nontarget patterns. These observations led to the hypothesis that the target in these experiments was detected by a serial mechanism which "scanned" a persisting but rapidly degrading neural representation of the visual scene with increasing detection failures the later in time the scan processed the location occupied by the target. If this hypothesis is correct, then target detectability should vary inversely with the number of stimuli which must be examined. The present experiment confirmed this expectation. A mathematical model of such a serial scanning process also predicts other, less obvious, effects on target detectability which were observed when the number of nontarget patterns was changed.

Adult

Detectability as a function of spatial location: effects of selective attention.

In a series of previous reports we have described differences in detectability of a target in a background of nontarget patterns as a function of its spatial location. These differences, referred to as a "detectability gradient," have been attributed to target detection accomplished by a serial processing mechanism--a scan. The mathematical model of such a mechanism, developed in the previous report, is equally applicable to a series of attentional shifts or to a perceptual, i.e., a preattentive, mechanism. The present experiments were designed to test the hypothesis that this scan is attentional in nature. The results provide additional evidence for the scanning hypothesis but do not support the view that this scan represents a series of attentional shifts.

Adult

Detectability as a function of target location: effects of spatial configuration.

Marked differences in detectability as a function of spatial location, a "detectability gradient," are observed when subjects are required to detect a briefly exposed target pattern of uncertain location in the presence of a number of nontarget patterns. Target detectability also is inversely related to the number of nontarget patterns which are present in this search paradigm. These previous findings provide strong evidence for a serial process in which increasing probability of error occurs during a scan of a rapidly degrading neural representation of the visual image following a brief exposure to the stimuli. It is not yet established whether this scan is attentional or perceptual in nature. The present experiments test the hypothesis of an attentional scan by presenting the target and nontarget patterns in spatially segregated groups. If the scan is attentional, then target detectability under these circumstances would be expected to exhibit the characteristic phenomenon of "group processing"--a close clustering of detection performance for targets located within a group and large differences in detectability across groups. As no evidence for group processing was observed, the results fail to support the view that the scan is attentional in nature but are fully consistent with a nonattentional scan.

Adult

Target detection in one visual field in the presence or absence of stimuli in the contralateral field by right- and left-handed subjects.

Marked differences in detectability are observed as a function of retinal locus when subjects are required to find a briefly exposed target pattern of uncertain location in the presence of a number of discriminably different nontarget patterns. Our previous studies using this search paradigm have attributed these detectability differences, and the right visual field detectability superiority associated with them, to a serial (scanning) mechanism which tends to examine stimuli in the right field earlier than those in the left. The present experiment, performed on large groups of right- and left-handed subjects, was designed to test the hypothesis that there are two independent serial processors, one in each hemisphere--an hypothesis which might account for the differences in detectability within and between the two half-fields in terms of hemispheric processing differences. The results are inconsistent with the dual independent serial processor hypothesis but are fully consistent with a single serial processor, a scanning mechanism, which has access to the information presented to both visual half-fields.

Adult

Visual detectability gradients: the effect of distractors in contralateral field.

A number of studies involving recognition of tachistoscopically presented words have reported that the typical right visual field performance superiority associated with linguistic stimuli is enhanced by bilateral presentations (simultaneous stimuli in both visual half-fields) compared to unilateral presentations (stimuli in only one half-field on a trial). We have reported the same phenomenon, however, using visual spatial patterns in a search paradigm (E. W. Yund, R. Efron, & D. R. Nichols, 1990c. Brain and Cognition, 12, 117-127) and have accounted for it in terms of the operating characteristics of a visual scanning mechanism which serially examines a decaying neural representation of the stimuli. In the present experiment we attempted to exploit these operating characteristics to influence this difference between unilateral and bilateral presentations. The results not only are consistent with the assumptions of the scanning hypothesis but they also provide new information pertinent to the operating characteristics of this mechanism.

Adult

Scanning the visual field without eye movements--a sex difference.

Subjects identified the location of a briefly exposed target pattern in the presence of five other patterns. Right-handed females, but not males, exhibited a significantly higher error rate in correctly localizing the target pattern when it was in the left visual field, particularly for the left parafoveal region. This unexpected distribution of errors as a function of target location can be accounted for by a sequential (serial) mechanism which scans the visual field. Since the exposure time was too brief for eye movements to have occurred, the results must reflect an internal scan of the neural representation of the information retained in the visual system following the brief stimulus presentation.

Adult

Speech discrimination with an 8-channel compression hearing aid and conventional aids in background of speech-band noise.

The design for a multichannel compression hearing aid was developed from previous experimental and theoretical work in our laboratory concerning pitch perception in normal-hearing subjects. The new hearing aid, implemented with off-line digital signal processing, was tested on twenty subjects with sensorineural hearing loss using speech sounds in a background of speech-spectrum noise. Five signal-to-noise ratios (+15 to -5dB) were used at two noise levels (60 and 70 dB SPL). Hearing-loss subjects listened to these stimuli under three different conditions: a) processed by the new multichannel compression hearing aid; b) processed by a conventional hearing aid; and c) unprocessed. The performance of normal-hearing subjects with the unprocessed stimuli provided another condition against which the performance in the two hearing aid conditions could be evaluated. Both aided conditions provided improved performance over the unprocessed condition and the multichannel compression aid produced better performance than the conventional aid. In the case of 4 of the 20 subjects, with less severe gradually sloping hearing losses, the new multichannel compression aid produced near-normal performance even at low signal-to-noise ratios. Some aspects of the results also suggested that learning to use the aid was more important in the case of the multichannel compression aid than in the case of the conventional aid. These results indicate that a multichannel compression hearing aid can be very effective in some individuals with sensorineural hearing loss and is superior to a conventional hearing aid in most subjects.

Acoustics

An ear asymmetry for gap detection following anterior temporal lobectomy.

A threshold elevation in the performance of auditory temporal order judgment in man has been reported in the ear contralateral to the side of an anterior temporal lobectomy. On the basis of temporal order judgments alone it is not possible to determine whether the deficit is attributable to an impairment of recognition, identification, or temporal resolution. The present monaural experiments compared the performance of the two ears in the detection of a gap in a broad-band noise burst in normal and temporal lobectomized subjects. The results revealed a right-left symmetry in gap detection performance by normal subjects but a significant deficit in gap detection in the ear contralateral to the side of an anterior temporal lobectomy--a finding interpreted as revealing the existence of a bonafide deficit in auditory temporal resolution induced by such resection.

Adult

Central auditory processing. I. Ear dominance--a perceptual or an attentional asymmetry?

The phenomenon of ear dominance for pitch described by Efron and Yund has been attributed by them to an asymmetry of sensory origin in the binaural integration of dichotic tone pairs. An explanation of this phenomenon in terms of an attentional bias is rejected on the basis of two experiments where the possibility of such bias was excluded. These and other experiments indicate that a simple explanation of this ear dominance in terms of a hemispheric specialization in the processing of tonal stimuli also must be rejected.

Attention

Central auditory processing. III. The "cocktail party" effect and anterior temporal lobectomy.

The capacity to selectively attend to only one of multiple, spatially separated. simultaneous sound sources--the "cocktail party" effect--was evaluated in normal subjects and in those with anterior temporal lobectomy using common environmental sounds. A significant deficit in this capacity was observed for those stimuli located on the side of space contralateral to the lobectomy, a finding consistent with the hypothesis that within each anterior temporal lobe is a mechanism that is normally capable of enhancing the perceptual salience of one acoustic stimulus on the opposite side of space, when other sound sources are present on that side. Damage to this mechanism also appears to be associated with a deficit of spatial localization for sounds contralateral to the lesion.

Attention

Central auditory processing. IV. Ear dominance--spatial and temporal complexity.

Ear dominance for dichotically presented tones was measured in 63 righthanded subjects when the frequency difference (delta f) was small compared to the center frequency (fc) and again when it was large. Although two-thirds of the population exhibited a left-ear dominance in both conditions, a shift toward right-ear dominance occurred when the delta f was increased. An additional study, employing the alternating tone illusion described by Deutsch, revealed the same general effect, i.e., a shift toward right-ear dominance with increasing values of delta f/fc. The results of these experiments, coupled with a review of previously published data of other dichotic experiments, indicate that as the ratio of delta f/fc increases, the subjective complexity of the sound image increases, and there is a progressive emergence of a "right-ear advantage" (or ear dominance). A tentative explanation relates these results to the effects of anatomical asymmetries of primary and auditory association cortex and the efferent temporal lobe enhancement mechanism described by R. Efron, P.H. Crandall, B. Koss, P.L. Divenyi, and E.W. Yund (Brain and Language, 1983, 19, 254-263.

Adolescent

The orientation and direction selectivity of cells in macaque visual cortex.

Quantitative data are presented on the orientation and direction specificity of the responses of cells in macaque monkey striate cortex. There is a bimodal distribution of direction-specific and nondirection-specific cells, with similar orientation tuning in each class. Cells range in orientation bandwidth at half amplitude from 6 degrees to 360 degrees (i.e. no orientation tuning), with a median near 40 degrees. Foveal-parafoveal and simple-complex subsamples show similar ranges of orientation bandwidths as well as similar medians (the bandwidths being somewhat broader than those found in cat cortex). The foveal subsample and a high-spatial-frequency subsample have more horizontal and vertical optimal orientations than oblique ones. Most cells show inhibition to some orientations, as well as excitation to others. Minimum-response orientations are generally less than 90 degrees from the optimal orientation--indicating maximum inhibition adjacent to the excitatory orientations. Three simple receptive field models are shown to differ in their abilities to account for these results.

Animals

Responses of striate cortex cells to grating and checkerboard patterns.

1. Cells in visual cortex have been alternately considered as bar and edge detectors, or as spatial-frequency filters responding to the two-dimensional Fourier component of patterns. 2. The responses to gratings and to checkerboards allow one to test these alternate models: the Fourier components of a checkerboard pattern do not occur at the same orientation as the edges, nor do the checkerboard spatial frequencies correspond to the check widths. 3. Knowing the orientation tuning of a cell for gratings, one can precisely predict its orientation tuning to checkerboards from the orientation of the fundamental Fourier components of the patterns, not from the orientation of their edges. This was found for both square and rectangular checkerboards, and held for both simple and complex cortical cells. 4. Knowing the spatial tuning of a cell for sine-wave gratings, one can precisely predict its spatial tuning to square and rectangular checkerboards from the spatial frequencies of the fundamental Fourier components of the patterns, not from the widths of their checks. 5. When presented with checkerboards in which not the fundamental but the upper harmonics were within its spatial bandpass, a cell's orientation tuning was found to be predictable from the (quite different) orientation of the higher Fourier harmonic components, but not from the orientation of the edges. 6. Knowing a cell's contrast sensitivity for gratings, one can predict the cell's contrast sensitivity for checkerboards much more accurately from the amplitudes of the two-dimensional Fourier components of the patterns than from the contrasts of the patterns. 7. The orientation tuning, spatial-frequency tuning and responsiveness of cells to a plaid pattern were also found to be predictable from the pattern's two-dimensional Fourier spectrum. 8. Both simple and complex striate cortex cells can thus be characterized as two-dimensional spatial-frequency filters. Since different cells responsive to the same region in the visual field are tuned to different spatial frequencies and orientations, the ensemble of such cells would fairly precisely encode the two-dimensional Fourier spectrum of a patch of visual space.

Action Potentials