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Biomedical subjects

W H Ehrenstein

Publications and source records attributed to W H Ehrenstein.

At least 37 records · Page 2Linked to original sources

Dynamic complexity of visuo-motor coordination: an extension of Bernstein's conception of the degrees-of-freedom problem.

Extending Bernstein's spatial conception of the degrees-of-freedom problem in the human motor system, we introduce a method developed from the theory of non-linear dynamics that allows one to quantify the spatio-temporal, i.e. dynamic, complexity of visuo-motor coordination. The correlation dimension D is used to measure the effective number of dynamic degrees of freedom in the coordination that a subject uses when performing a visuo-motor tracking task. The validity of the estimator employed is demonstrated. Visuo-motor coordination had a low-dimensional (mean D-SD=6.07 -0.82) dynamic structure, which was consistent with deterministic chaos rather than with pure stochastic noise. D correlated with tracking performance, P. Both D and P were closely related to the degree of visuo-motor compatibility that the task presented to the subject. However, for short periods of training P increased, but D did not. As these seemingly contradictory results suggest, our dynamic conception of the degrees-of-freedom problem may reveal far more intricate visuo-motor interactions than Bernstein could identify on the basis of his spatial analyses of bodily movement patterns and by the methods of evaluation that were available to him at the time.

Adult↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗

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↗

Visual localization and estimation of extent of target motion during ocular pursuit: a common mechanism?

The ability to localize a visual target and to estimate the distance through which it moves was studied during ocular pursuit. In the first experiment observers had to localize the position of a visually tracked moving target when they heard an acoustic signal. The signal was sounded near the beginning or near the end of the motion. The distance between the perceived positions was shorter than the distance between the corresponding physical positions of the target. The 'shortening' became more pronounced with higher tracking velocity. In another condition the observers estimated the length of the motion path between two successive sound signals, one presented near the beginning and one near the end of the motion. The length of path travelled was underestimated, the effect being stronger with higher tracking velocity. In the second experiment this effect of velocity on the underestimation of distance was shown to exist only during ocular pursuit and not during steady fixation. The hypothesis that localization and estimation of distance during ocular pursuit share a common mechanism is discussed.

Acceleration↗

Spatial S-R compatibility with orthogonal stimulus-response relationship.

Spatial stimulus-response (S-R) compatibility with unimanual two-finger choice reactions was investigated under conditions in which the spatial orientation of response keys was either parallel to or perpendicular to the orientation of the stimuli. Subjects responded to green or red lights in the left or right visual field (irrelevant stimulus location). The response keys were oriented horizontally on the left or right side of the body midline parallel to the stimuli, and were pressed with the palms facing down (Condition A), or were oriented orthogonally to the stimuli in the midsaggital plane, either horizontally and pressed with palms facing down (B) or facing up (C), or vertically and pressed with palms facing the body (D). The results for Condition A demonstrate the usual spatial S-R compatibility effect between field of stimulation and spatial position of responding finger. For Conditions B and D, a strong reaction time advantage still obtained for those stimulus-finger pairings that are compatible under Condition A. Condition C revealed an RT advantage for the opposite pairings. This shift of the compatibility effect from Condition B to Condition C indicates that the left/right distinction of fingers does not follow a simple, fixed spatio-anatomical mapping rule. The results are discussed within the framework of a hierarchical model of spatial S-R compatibility, with spatial coding and spatio-anatomical mapping as factors.

Adult↗