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Biomedical subjects

W H Ehrenstein

Publications and source records attributed to W H Ehrenstein.

At least 19 recordsLinked to original sources
PubMed1999

Development of dynamic vision based on motion contrast.

The development of dynamic vision was investigated in 400 healthy subjects (200 females and 200 males) aged between 4 and 24 years. The test consisted of a computer-generated random-dot kinematogram in which a Landolt ring was briefly presented as a form-from-motion stimulus. Motion contrast between the ring and background was varied in terms of the percentage of dots moving coherently within the ring in four levels (100%, 50%, 30%, and 20%). The subject's task was to indicate the position of a gap in the ring (left, right, top, bottom). Results show a clear increase in performance with age for all motion contrast levels, with the greatest changes for the lowest levels. Adult performance was reached at the age of 15 years. Luminance-based static acuity measured with the Landolt test was poorly correlated with acuity for its form-from-motion analogue.

Adolescent↗
PubMed1998

A computer-assisted test for the electrophysiological and psychophysical measurement of dynamic visual function based on motion contrast.

A new test is described that allows for electrophysiological and psychophysical measurement of visual function based on motion contrast. In a computer-generated random-dot display, completely camouflaged Landolt rings become visible only when dots within the target area are moved briefly while those of the background remain stationary. Thus, detection of contours and the location of the gap in the ring rely on motion contrast (form-from-motion) instead of luminance contrast. A standard version of this test has been used to assess visual performance in relation to age, in screening professional groups (truck drivers) and in clinical groups (glaucoma patients). Aside from this standard version, the computer program easily allows for various modifications. These include the option of a synchronizing trigger signal to allow for recording of time-locked motion-onset visual-evoked responses, the reversal of target and background motion, and the displacement of random-dot targets across stationary backgrounds. In all instances, task difficulty is manipulated by changing the percentage of moving dots within the target (or background). The present test offers a short, convenient method to probe dynamic visual functions relying on surprathreshold motion-contrast stimuli and complements other routine tests of form, contrast, depth, and color vision.

Adolescent↗
PubMed1998

Influence of head-to-trunk position on sound lateralization.

The effect of horizontal head position on the lateralization of dichotic sound stimuli was investigated in four experiments. In experiment 1, subjects adjusted the interaural level difference (ILD) of a stimulus (band-pass noise) to the subjective auditory median plane (SAMP) while simultaneously directing the beam of a laser attached to the head to visual targets in various directions. The adjustments were significantly correlated with head position, shifting in a direction toward the side to which the head was turned. This result was replicated in experiment 2, which employed a two-alternative forced-choice method, in which stimuli of different ILD were presented and left/right judgments were made. In both experiments, the average magnitude of the shift of the SAMP was about 1 dB over the range of head positions from straight ahead to 60 degrees to the side. The shift of the SAMP indicates that any shift in head position induces a change in sound lateralization in the opposite direction, i.e., the intracranial sound image is shifted slightly to the left when the head is directed to the right and to the right when the head is to the left. In experiments 3 and 4, the effect of head position was compared with that of eye position by using the same methods as in experiment 2. Both shifts in SAMP, induced by either head- or eye-position changes, are in the same direction and, on average, of about the same magnitude (experiment 3), and head- and eye-position effects compensate approximately for each other during variations of head position when the gaze remains fixed to a visual target in space (experiment 4).

Acoustic Stimulation↗
PubMed1998

Auditory-visual spatial integration: a new psychophysical approach using laser pointing to acoustic targets.

The alignment of auditory and visual spatial perception was investigated in four experiments, employing a method of laser pointing toward acoustic targets in combination with various tasks of visual fixation in six subjects. Subjects had to fixate either a target LED or a laser spot projected on a screen in a dark, anechoic room and, while doing so, direct the laser beam toward the perceived azimuthal position of the sound stimulus (bandpass-filtered noise; bandwidth 1-3 kHz; 70 dB sound pressure level, duration 10 s). The sound was produced by one of nine loudspeakers, located behind the acoustically transparent screen between 22 degrees to the left and 22 degrees to the right of straight ahead. Systematic divergences between sound azimuth and laser adjustment were found, depending on the instructions given to the subjects. The eccentricity of acoustic targets was generally overestimated by up to 10.4 degrees with an only slight influence of gaze direction on this effect. When the sound source was straight ahead, gaze direction had a substantial influence in that the laser adjustments deviated by up to 5.6 degrees from sound azimuth, toward the side to which the gaze was directed. This effect of eye position decreased with increasing eccentricity of the sound. These results can be explained by the interactive effects of four distinct factors: the lateral overestimation of the auditory eccentricity, the effect of eye position on sound localization, the effect of the retinal eccentricity on visual localization, and the extraretinal effect of eye position on visual localization.

Acoustics↗
PubMed1997

Motion extrapolation and velocity transposition.

A study of the effect of the size of a moving target and the extent of its visible motion on motion extrapolation is reported. Targets (a horizontal pair of dots separated by either 0.2 or 0.8 deg) moved across a 10 deg rectilinear path and were then occluded. Observers pressed a key when they thought the leading dot of a hidden target had reached a randomly specified position (0-12 deg from the point of occlusion). In experiment 1, in agreement with velocity-transposition predictions, at moderate (5 deg s-1) and rapid (10 deg s-1) velocities extrapolation times were longer for large targets than for small ones. At slow velocity (2.5 deg s-1) this effect was reversed. In experiment 2 the effect of target size at moderate velocity was found for a short (2.5 deg) visible path. However, the extrapolation time increased with shorter (2.5 deg versus 10 deg) paths. A proposed account of these effects suggests that the visual system performs a spatiotemporal scaling, according to the velocity-transposition principle, not only of visible motion but also of extrapolated motion.

Adult↗
PubMed1996

Auditory-visual shift in localization depending on gaze direction.

The effect of eye position on the spatial congruence of the perceived direction of auditory and visual cues was investigated, using a two-alternative forced choice method in combination with a visual fixation task. The azimuth of the sound was perceived as slightly shifted to the left of a visual reference when the gaze was directed to the left, and to the right when the gaze was to the right. The maximum magnitude of this relative auditory-visual shift was 4.7 degrees over a range of fixation angles from 45 degrees to the left to 45 degrees to the right. The observed auditory-visual shift may reflect an incomplete transformation of spatial coordinates within auditory and visual neural representations, as suggested by neurophysiological recordings in the primate midbrain.

Adult↗
PubMed1996

Monkey saccadic latency and pursuit velocity show a preference for upward directions of target motion.

Saccadic latency was studied as a function of the direction of sudden target displacements (steps) and of subsequent smooth target motion (ramps) in Macaca fascicularis. The monkey fixated a central spot that suddenly changed its position and then moved constantly at 10 deg s-1, thus eliciting initial saccades and subsequent pursuit eye movements (recorded by a magnetic search-coil technique). Latencies for initial saccades differed markedly in the vertical axis, being shorter in upward than downward directions for both step and ramp components of target motion. Saccadic latency was also related to the mean pursuit velocity, indicating that the oculomotor system accounts for the direction of step and ramp components of target motion in an integrative way.

Animals↗
PubMed1996

The effect of eye position on auditory lateralization.

The present study examines whether the direction of gaze can influence sound lateralization. For this purpose, dichotic stimuli with variable interaural level difference (ILD) were presented under different conditions of visual fixation. In experiment 1, subjects with their head fixed directed their gaze to a given target, simultaneously adjusting the ILD of continuous pure tone or noise stimuli so that their location was perceived in the median plane of the head. The auditory adjustments were significantly correlated with gaze direction. During eccentric fixation, the psychophysical adjustments to the median plane shifted slightly toward the direction of gaze. The magnitude of the shift was about 1-3 dB, over a range of fixation angles of 45 degrees to either side. The eye position effect, measured as a function of pure-tone frequency, was most pronounced at 2 kHz and showed a tendency to decrease at lower and higher frequencies. The effect still occurred, although weaker, even when the eyes were directed to eccentric positions in darkness and without a fixation target. In experiment 2, the adjustment method was replaced by a two-alternative forced-choice method. Subjects judged whether sound bursts, presented with variable ILDs, were perceived on the left or right of the median plane during fixation of targets in various directions. Corresponding to experiment 1, the psychometric functions shifted significantly with gaze direction. However, the shift was only about half as large as that found in experiment 1. The shift of the subjective auditory median plane in the direction of eccentric gaze, observed in both experiments, indicates that dichotic sound is localized slightly to the opposite side, i.e., to the left when the gaze is directed to the right and vice versa. The effect may be related to auditory neurons which exhibit spatially selective receptive fields that shift with eye position.

Acoustic Stimulation↗
PubMed1996

A cross-modal aftereffect: auditory displacement following adaptation to visual motion.

It has been shown earlier that the perceived location of static sound-sources can be displaced (a) during visual motion and (b) following auditory motion. Here we combine these phenomena. The subject adapted to the horizontal visual motion of a surrounding drum, then (with the lights off) localized static sound-sources by setting the direction of a pointer. Adapting motion was clockwise or counterclockwise: the difference between each subject's settings following the opposite directions of adaptation showed small but consistent auditory displacements opposite to the adapting directions. This visual-auditory aftereffect, which is consistent with sensorineural data, challenges a general, if implicit, belief that aftereffects do not cross modalities.

Adolescent↗
PubMed1996

The growing-louder effect in short diotic stimuli.

Previous evidence from short monotic stimuli shows that a steady stimulus is perceived as growing louder; to be perceived as steady, the intensity of the stimulus must decrease. In the present study, 10 subjects heard a sequence of diotic tonal stimuli. Each stimulus lasted 1.5 sec. and increased, decreased, or remained steady in intensity; initial intensity was 40 dB SPL and carrier frequency was 1 kHz. Subjects made forced binary responses of "growing louder" or "growing softer" to each stimulus. Confirming the evidence from monotic stimuli, the mean value of changing intensity eliciting equal numbers of both responses was negative. Possible explanations for this growing-louder effect reside in (a) the percussive nature of many natural sounds and (b) selective responding to approaching sound-sources.

Adult↗
PubMed1995

Varying the strength of the Munker-White effect by stereoscopic viewing.

In the Munker-White effect grey target bars appear lighter when they are flanked by white bars, and darker when they are flanked by black bars. It is shown that the effect is enhanced if the patterns are presented stereoscopically so that the grey bars appear either behind the grating, in which case they are seen as a rectangle that is occluded by the white bars of the grating, or in front of the grating, so that they form a transparent rectangle. These results are explained in terms of object perception: contrast enhances differences between an object and its surroundings, whereas assimilation reduces differences within an object.

Adult↗
PubMed1994

The Simon effect and visual motion.

S-R compatibility and Simon effects were studied for real visual motion. In Experiment 1, two small stimulus lights were constantly visible, 5 degrees to the left and right of fixation; after a random delay, one began to move at 2 degrees/s. In Experiment 2, a single stimulus light moving at 2 degrees/s suddenly appeared 5 degrees to the left or right of fixation, i.e., motion onset and stimulus onset coincided. In both experiments, subjects responded by a key press with their left or right index finger as soon as they detected motion. In Condition A responses were made to the position (left or right) from which the motion started, irrespective of its direction (position compatibility); in Condition B responses were made to the direction of motion (leftward or rightward) irrespective of whether motion started to the left or to the right of fixation (direction compatibility). The results show strong compatibility effects for both position and direction of motion in both experiments. A Simon effect, however, occurred only when position was task irrelevant in Experiment 1; no Simon effect was found in Experiment 2. The data only partly confirm previous results obtained with apparent motion. The selective lack of a Simon effect supports the integrated model of Umiltà and Nicoletti (1992), which requires orienting of attention for the Simon effect to occur. It is specifically assumed that this attention-orienting is triggered only by the saccade program and does not extend to the pursuit program that is initiated by smooth stimulus motion.

Adolescent↗
PubMed1994

Experiments on the afterimages of stimulus change (Dvorák 1870): a translation with commentary.

In 1870 Dvorák rejected Helmholtz's eye-movement account of motion aftereffects (MAEs) on the grounds that it was inconsistent with previous reports of nonuniform rotation in MAEs induced with Plateau spirals. Subsequent observations with spirals that were modified to induce both expanding and contracting MAEs simultaneously, together with the use of stationary negative afterimages during induction and test, were offered as further counter-examples to the eye-movement hypothesis. Dvorák's conjectures that perception (and misperception) of movement involves a unitary perceptual dimension of stimulus change also led him to investigate whether aftereffects comparable to MAEs could be induced along other stimulus dimensions in vision (luminance gradients), and in audition (gradients of pitch and intensity). It is suggested that Dvorák's observations, taken as a whole, may be interpreted as an attempt to provide evidence challenging the Helmholtzian traditions underpinning eye-movement accounts of MAEs. The nature and outcomes of these observations are provided in a translation of the original work, and are subsequently discussed in relation to some contemporary empirical counterparts.

Auditory Perception↗
PubMed1994

Auditory aftereffects following simulated motion produced by varying interaural intensity or time.

Simulated auditory motion, ie step-ramp modulated interaural intensity (delta I) or time (delta t) was presented via headphones as an adapting stimulus (narrow-band signal of 1 kHz mean frequency). After adaptation, settings of a stationary test stimulus were systematically shifted in the opposite direction when the experimental parameter was delta I, but not when it was delta t. Further studies with delta t motion with the use of mean frequencies of 100 Hz or 6 kHz showed an aftereffect only at 6 kHz. Unlike visual motion aftereffects, no counter-motion was observed; rather the test stimulus appeared stationary, but settings of its interaural midline were displaced in a direction opposite to the direction of adaptation (on average by 1.2 dB or 30 microseconds for delta I-stimulated and delta t-stimulated motion, respectively). This displacement effect decayed with time after adaptation. The frequency dependence found for delta t motion suggests that the low-frequency mechanism of directional hearing that uses interaural ongoing-time (phase) differences is not able to adapt. The observed auditory aftereffects may be analogous to visual motion aftereffects since they are direction specific; however, because they lack apparent motion they also resemble disparity-specific stereoscopic aftereffects.

Adolescent↗
PubMed1993

Motion-onset visual-evoked potentials as a function of retinal eccentricity in man.

Visual-evoked potentials were elicited by the motion-onset of a black-and-white square-wave grating of 2.4 cycles/deg that drifted from right to left at a velocity of 3 deg/s. The center of the 2 x 2 deg stimulus field was binocularly viewed either foveally or at eccentricities of 6, 12, or 20 deg in the lower visual field along the vertical meridian. Peak-to-peak amplitudes P1-N2 and N2-P2 were found to decrease non-linearly as a function of eccentricity. The VEP-amplitudes were standardized by setting each foveal value to 100%, and a relative measure was derived for peripheral values given by the ratio of the peripheral to the foveal values. The decrease of the relative VEP-values with eccentricity was significantly smaller than that of the relative cortical magnification factor of striate cortex in man, whereas it agreed fairly well with that of the relative point-image size of the area MT in Macaque monkey. In this respect, the motion-onset VEP is distinct from the pattern-reversal VEP, the amplitude of which decreases much more rapidly with retinal eccentricity; hence, it may involve different generating structures of the brain.

Adolescent↗
PubMed1991

Selective directional sensitivity in visual motion perception.

We present two experiments demonstrating that: (i) the latency of perception of the position of a small visual target moving towards the fovea is shorter than that of the same target moving away from the fovea; (ii) the reaction time (RT) to onset of motion of the same type of target is also shorter when it moves towards the fovea; and (iii) the RT to onset of motion away from the fovea may be shorter when larger, textured stimuli are employed. The relation of the findings to the existence of two systems for visual motion information processing and to recent neurophysiological findings is discussed.

Adult↗
PubMed1991

Perceptual constancy during ocular pursuit: a quantitative estimation procedure.

Perceptual constancy of visual motion is usually described as the degree of correspondence between physical and perceived characteristics of motion in the external world. To study it, one has to assess the relationship between physical motion, its retinal image, and its perception. We describe a quantitative estimation procedure for a measure K denoting the degree of perceptual constancy of background target motions noncollinear to the eye movements during ocular pursuit. The calculation of K is based on three vectors describing the target motion (1) as it is physically, (2) as it is mapped to the retina, and (3) as it is perceived, but only the direction of the perceptual motion vector has to be determined experimentally. K allows for quantitative comparison between experiments with a variety of parameters in visual motion displays.

Eye Movements↗