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S Magnussen

Publications and source records attributed to S Magnussen.

At least 19 recordsLinked to original sources
PubMed1992

Retention and disruption of motion information in visual short-term memory.

Velocity discrimination thresholds for drifting luminance gratings were measured as a function of the time interval between test and reference gratings, using a two-interval, forced-choice procedure. Discrimination thresholds, expressed as Weber fractions (delta V/V), were independent of interstimulus intervals (ISIs) ranging from 1-30 s, demonstrating perfect short-term retention of velocity information. When a third grating was briefly presented halfway through a 10-s ISI, memory masking was observed. Discrimination thresholds in memory masking were unaffected by maskers of the same velocity but increased by 100% when test and masker velocity differed by a factor of 2. The results are interpreted with reference to a model where the short-term memory for simple stimulus attributes is assumed to be organized in terms of arrays of memory stores linked in a lateral inhibitory network.

Acceleration↗
PubMed1992

A distribution model for heritability.

A regression model to predict quantiles of narrow sense individual and family mean heritabilities is developed and used to predict confidence intervals either directly or via a generalized beta distribution model. Extensive simulations of balanced sib analysis trials in randomized complete block designs and normal distributed environmental and additive genetic effects confirmed that heritabilities follow a beta distribution even in cases with up to 10% of the data missing at random. The new model is both more accurate and more precise than commonly used alternatives based on "exact" chi 2 distributions and Satterthwaites approximations to the degrees of freedom. Estimates of the expected heritability and a Taylor approximation of the standard error of the heritability are needed as input to the quantile model. Applications of the presented models for estimating confidence intervals and as an aid in the design of experiments are provided.

Genetics, Population↗
PubMed1991

Stimulus-specific mechanisms of visual short-term memory.

The retention of spatial information in visual short-term memory was assessed by measuring spatial frequency discrimination thresholds with a two-interval forced-choice task varying the time interval between the two gratings to be compared. The memory of spatial frequency information was perfect across 10-sec interstimulus intervals. Presentation of a "memory masker" grating during the interstimulus interval may interfere with short-term memory. This interference depends on the relative spatial frequency of the test and masker gratings, with maximum interference at spatial frequency differences of 1-1.5 octaves and beyond. This range of interference with short-term memory is comparable to the bandwidth of sensory masking or adaptation. A change of the relative orientation of test and masker gratings does not produce interference with spatial frequency discrimination thresholds. These results suggest stimulus-specific interactions at higher-level representations of visual form.

Discrimination, Psychological↗
PubMed1991

The time course of adaptation to spatial contrast.

We explored the buildup and decay of threshold elevation during and after adaptation to sinewave gratings in a series of experiments investigating the effects of adapting time, adapting contrast, spatial frequency and retinal eccentricity. Contrast thresholds for vertical sinewave gratings truncated in space by a one-dimensional Gaussian envelope were measured before and after adaptation to a full-field suprathreshold grating of the same spatial frequency and orientation. Thresholds were measured intermittently after adaptation in a "seen/not-seen" single presentation procedure until these thresholds returned to baseline values. The first test grating was presented 300 msec after the offset of the adapting stimulus, and thereafter at regular intervals. At different times after adaptation, contrast thresholds were estimated by off-line analysis of the data using the QUEST algorithm. Adapting time was either 1, 10, 100 or 1000 sec and adapting contrast was either 9, 19, 29 or 39 dB (re. 1%). The test gratings were presented centered either at the fixation point or at 5 and 10 deg eccentricity along the horizontal meridian. The results suggest that up to the saturation level the buildup and the decay of adaptation to contrast is well described by a power function of time. The slope of the best fitting line on log-log axes is fairly constant for the adaptation times tested. As reported earlier, thresholds increased with adapting contrast and these contrast-dependent differences were evident 300 msec after the termination of adaptation. Adaptation at 10 deg eccentricity yielded slightly higher threshold elevations than for central vision. Based on these results, a description is given of the dynamic response of the underlying neural mechanisms.

Adaptation, Ocular↗
PubMed1989

Detection of moving and stationary gratings in the absence of striate cortex.

A 30-yr-old woman whose left occipital lobe had been removed because of an arteriovenous malformation was tested for her ability to detect stationary flashing and moving luminance gratings in the right (blind) visual field. With stationary gratings the performance remained close to chance level, but with moving gratings her performance on a 2AFC task rose to an average of close to 68% during 1200 trials. Signals mediated via midbrain structures might be the basis for the above-chance detection of movement.

Adult↗
PubMed1988

Interactions among spatial frequency and orientation channels adapted concurrently.

Interactions between size and orientation-specific mechanisms in the human visual system were investigated using a sequential adaptation technique. Subjects adapted to a vertical, 4 c/deg high-contrast (0.7) sinewave grating that was interleaved at a rate of 0.5 Hz with another adapting grating differing either in (1) spatial frequency or (2) orientation. Before and after adaptation contrast thresholds were measured for a vertical 4 c/deg sinewave test grating. The resultant elevation in contrast threshold was plotted as a function of the (1) spatial frequency or (2) orientation differences between the first and second adapting gratings. Maximum threshold elevation was found when both adapting gratings shared the same spatial frequency and orientation. Minimum elevations were found when the second grating's spatial frequency or orientation differed by approx. 1.5 octaves or 45 deg, respectively. Beyond these values threshold elevations reapproached the baseline value measured in a control condition, where the 4.0 c/deg adapting grating was interleaved with a blank. The minimum threshold elevations were 0.2-0.3 log units below the baseline level. The results suggest the existence of inhibitory interactions between neural mechanisms tuned to the size and orientation of retinal images.

Adaptation, Ocular↗
PubMed1988

[Blue cone monochromasia: diagnosis, genetic counseling and optical aids].

Cone and rod functions of three blue cone monochromats (age 13-20, male) from three different families were investigated. In contrast to rod monochromats, they lack prominent nystagmus. Color matches as determined using the Nagel anomaloscope came close to those of rod monochromats but the green primary appeared slightly brighter to them. In color discrimination tests (Farnsworth-Munsell 100-hue and Panel D-15 desaturated), maximum confusion followed protan rather than scotopic axes. Measurements of spectral sensitivity revealed action spectra exclusively of blue sensitive cones, even under conditions that should isolate green- or red-sensitive cones. After 20 minutes of dark adaptation, rods determined the spectral sensitivity function. Transient tritanopia, which in normals results from the interaction between cones sensitive to short and long wavelengths, was completely absent in blue cone monochromats. Visual acuity (Snellen charts and contrast gratings) revealed values between 20/200 and 20/60. Recognition of high-spatial low-contrast gratings was improved by blue cut-off filters (Schott BG 28) and considerably worsened by yellow cut-off filters (Schott OG 510). Since alteration of visual acuity induced by cut-off filters was not found in rod monochromats, this two-filter test is a means of differentiating quickly between rod achromats and blue cone monochromats. As the mode of inheritance is autosomal recessive in rod achromats and x-linked recessive in blue cone monochromats, differential diagnosis is important for correct genetic counseling.

Adult↗
PubMed1988

Spatial vision of the achromat: spatial frequency and orientation-specific adaptation.

1. The psychophysical technique of selective adaptation to stationary sine-wave gratings of varying spatial frequency and orientation was used to investigate the central processing of spatial information in the visual system of the complete achromat. 2. For adapting spatial frequencies of 1 and 2 cycles/deg, the spatial frequency and orientation selectivity of contrast threshold elevation is similar for achromatic and trichromatic vision. 3. For adapting frequencies below 1 cycle/deg, the achromat shows threshold elevations of normal magnitude with symmetrical spatial frequency and orientation tuning for adapting frequencies as low as 0.09 cycles/deg with 'bandwidth' estimates similar to those found at high frequencies in the trichromat. Below 0.66 cycles/deg no after-effect could be obtained in the trichromat, and the frequency tuning at 0.66 cycles/deg was skewed towards higher frequencies. 4. The interocular transfer of low-frequency adaptation in the achromat was 50%, which is the same value obtained at higher frequencies. 5. The time course of the decay of low spatial frequency adaptation in the achromat was similar to that found at higher frequencies. 6. Control experiments show no low-frequency adaptation in peripheral vision or in central vision in the dark-adapted trichromat indicating that low spatial frequency adaptation cannot be elicited through the rod system of the trichromat. 7. It is proposed that the observed range shift of adaptable spatial frequency mechanisms in the achromat's visual cortex is the result of an arrest at an early stage of sensory development. The visual cortex of the achromat is comparable, with respect to spatial processing, to that of the young, visually normal human infant.

Adaptation, Ocular↗
PubMed1988

Spatial waveform discrimination following higher-harmonic adaptation.

Campbell and Robson [J. Physiol. (London) 197, 551 (1968)] proposed that a near-threshold square-wave grating can be distinguished from a sine-wave grating of the same spatial frequency and fundamental amplitude when the channel tuned to the third-harmonic component of the square wave reaches its own threshold. To test this hypothesis, we measured waveform discrimination thresholds with two-interval forced-choice methods before and after 4-min adaptation to a high-contrast sine-wave grating, the spatial frequency of which equaled that of the square wave's third harmonic. The results indicate that 3f adaptation has only a negligible effect on discrimination thresholds. In a further experiment, we adapted observers to both 3f and 5f harmonic frequencies of the square-wave test grating presented sequentially over 4 min. Although substantial threshold elevations occurred at the 3f and 5f frequencies, the elevation in waveform discrimination threshold was small. These results suggest that the independent-channel hypothesis alone cannot account for the visibility of complex features (edges) following harmonic adaptation.

Adaptation, Physiological↗
PubMed1987

Saturation of the tilt aftereffect.

The tilt aftereffect increases as a logarithmic function of adapting time, reaches saturation after approx 1 hr and decays on a symmetric, logarithmic time-course. This is similar to the time-course of contrast threshold elevation, suggesting that threshold and suprathreshold aftereffects are based on similar type of adaptation processes.

Adaptation, Ocular↗
PubMed1987

Higher-harmonic adaptation and the detection of squarewave gratings.

Adaptation to a high contrast sinewave grating of 1 c/deg spatial frequency causes a large increase in the contrast threshold for a 1 c/deg test grating, but fails to raise the threshold for a squarewave grating of 0.33 c/deg, although the sensitivity of the "channel" tuned to both the third and fifth harmonic components of the squarewave test grating should be thoroughly suppressed. Following sequential adaptation to sinewave gratings of 1 and 3 c/deg spatial frequency, detection of squarewave gratings at 0.33 c/deg likewise remains unaffected. In contrast, after adaptation to a 0.33 c/deg squarewave grating with missing fundamental the contrast threshold for a squarewave test grating of the same frequency is increased by 0.25 log unit, although the higher harmonic component frequencies are less affected than by sequential sinewave adaptation. The results suggest that independent spatial frequency channels detecting harmonic components are not alone sufficient to account for the visibility of low frequency squarewaves.

Adaptation, Ocular↗
PubMed1986

Temporal aspects of spatial adaptation. A study of the tilt aftereffect.

Growth and decay characteristics of the tilt aftereffect were studied for aftereffects induced by normal or continuous adaptation routines, and for aftereffects induced by successive or spaced adaptation to the same or different orientations on an adapt-partial decay-readapt schedule. In the continuous adaptation condition, growth and decay of the aftereffect were logarithmic functions of time. There was no evidence for saturation after 30 min adaptation. Aftereffect decay following spaced adaptation progresses as by continuous adaptation, but an adapting stimulus introduced during recovery from previous adaptation is more effective on the time scale than when introduced to a fully recovered system, summing approximately linearly with the residual aftereffect and off-setting the recovery process to zero. A second adapting stimulus whose orientation is of opposite sign (ccw vs cw) induces a two-phased decay process consisting of an early cancellation and a later enhancement of the original aftereffect. A two-stage model of adaptation is proposed.

Adaptation, Ocular↗
PubMed1986

Contrast threshold elevation following continuous and interrupted adaptation.

Contrast thresholds for a 6 c/deg sinewave grating were measured following continuous and interrupted adaptation of 10 min duration to a high-contrast (0.6) sinewave grating of the same spatial frequency. Interrupted adaptation was administered as five 2-min segments, and the interadaptation interval (IAI) was varied from 10 to 180 sec. The results indicate that adaptation to spatial contrast can be described by a two-staged process, each stage having a different time constant of adaptation decay.

Adaptation, Ocular↗
PubMed1985

Marathon adaptation to spatial contrast: saturation in sight.

The contrast thresholds for detecting a 6.0 c/deg vertical sinusoidal test grating were tracked during and after 3 hr inspection of a high-contrast adapting grating of the same spatial frequency and orientation. Log contrast threshold increased linearly with log adaptation time, attaining a final stable value after approximately 30 and 60 min of adaptation for the two subjects tested. The recovery function was likewise linear on double logarithmic axes. The results further suggest that adaptation beyond the saturation point had no influence on the subsequent rate of recovery.

Adaptation, Ocular↗
PubMed1985

Visual half-field symmetry in orientation perception.

The perception of orientation in the left and right visual half-fields has been investigated. No evidence for interfield differences was obtained for the discrimination of single lines by line matching or in magnitude of the systematic orientation distortion in orientation contrast and rod-and-frame experiments. Furthermore, increasing the time interval between test and comparison lines in successive matching provides no evidence for a differential operation of short-term spatial memory in the two hemispheres. It is concluded that hemispheric asymmetries do not arise at the level of sensory processing of spatial signals.

Female↗
PubMed1979

A test for contrast-polarity selectivity in the tilt aftereffect.

The tilt aftereffect (TAE) was studied with adapting and test stimuli consisting of black or white bars (experiment 1), and of luminance edges (experiment 2). Both experiments failed to demonstrate selectivity of the TAE to the polarity of luminance contrast.

Adaptation, Ocular↗