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Biomedical subjects

B Crassini

Publications and source records attributed to B Crassini.

At least 19 recordsLinked to original sources

Barber-pole illusions and plaids: the influence of aperture shape on motion perception.

The barber-pole illusion and its influence on plaid perception were investigated in two experiments to test the following expectations: (i) apertures which bias the perception of grating motion in directions consistent with plaid direction will facilitate plaid perception, and (ii) apertures which bias the perception of grating motion in directions inconsistent with plaid direction will disrupt plaid perception. In experiment 1 the barber-pole illusion was measured as a function of grating orientation (20 degrees, 45 degrees, and 70 degrees, clockwise and counterclockwise from horizontal), and aperture shape (vertical, horizontal; at each of three elongations). Barber-pole illusions reported with 45 degrees gratings increased with increased aperture elongation. However, this was not found with 20 degrees and 70 degrees gratings; these were almost always reported as moving in a direction parallel to the side of the aperture with which the gratings formed angles approaching 90 degrees. In experiment 2 this dependence of barber-pole illusions on the relative orientation between gratings and apertures was also evident with 45 degrees gratings in oblique apertures; only oblique directions of grating motion were reported. The influence of the same apertures on the separate contrast thresholds required for initial plaid coherence and initial plaid decomposition was measured. In experiments 1 and 2, coherence thresholds were unaffected by apertures, contrary to expectation (i). However, in both experiments expectation (ii) was confirmed; decomposition thresholds decreased in apertures which biased perceived direction of gratings towards vertical (plaid direction), and increased in apertures which biased grating motion away from vertical. Adaptation of plaid mechanisms during measurement of decomposition thresholds was proposed to explain the discrepancy between coherence and decomposition data. Taken together, the results were interpreted as reflecting interactions between mechanisms mediating the barber-pole illusion and mechanisms mediating plaid perception.

Humans

Anomalous spiral aftereffects: a new twist to the perception of rotating spirals.

Stationary spirals viewed after inspecting rotating sectored disks appear to rotate and to expand or contract radially, even though the rotating disks contain no perceptible components of radial motion. Moreover, the relative directions of illusory rotation and radial motion observed in these instances are 'impossible' under the stimulus constraints normally imposed by the geometry of a spiral under rotation: the stationary spirals appeared to expand/contract in directions opposite to those normally observed under conditions of actual spiral rotation, and under conditions of illusory spiral rotation in classical spiral aftereffects.

Discrimination Learning

Spatial-frequency-contingent color aftereffects: adaptation with one-dimensional stimuli.

The McCollough effect was shown to be spatial-frequency selective by Lovegrove and Over (1972) after adaptation with vertical colored square-wave gratings separated by 1 octave. Adaptation with slide-presented red and green vertical square-wave gratings separated by 1 octave failed to produce contingent color aftereffects (CAEs). However, when each of these gratings was adapted alone, strong CAEs were produced. Adaptation with vertical colored sine-wave gratings separated by 1 octave also failed to produce CAEs, but strong effects were produced by adaptation with each grating alone. By varying the spatial frequency of the test sine wave, CAEs were found to be tuned for spatial frequency at 2.85 octaves after adaptation of 4 cycles per degree (cpd) and at 2.30 octaves after adaptation of 8 cpd. Adaptation of both vertical and horizontal sine-wave gratings produced strong CAEs, with bandwidths ranging from 1.96 to 2.90 octaves and with lower adapting contrast producing weaker CAEs. These results indicate that the McCollough effect is more broadly tuned for spatial frequency than are simple adaptation effects.

Adaptation, Ocular

Spatial-frequency-contingent color aftereffects: adaptation with two-dimensional stimulus patterns.

The spatial-frequency theory of vision has been supported by adaptation studies using checkerboards in which contingent color aftereffects (CAEs) were produced at fundamental frequencies oriented at 45 degrees to the edges. A replication of this study failed to produce CAEs at the orientation of either the edges or the fundamentals. Using a computer-generated display, no CAEs were produced by adaptation of a square or an oblique checkerboard. But when one type of checkerboard (4 cpd) was adapted alone, CAEs were produced on the adapted checkerboard and on sine-wave gratings aligned with the fundamental and third harmonics of the checkerboard spectrum. Adaptation of a coarser checkerboard (0.80 cpd) produced CAEs aligned with both the edges and the harmonic frequencies. With checkerboards of both frequencies, CAEs were also found on the other type of checkerboard that had not been adapted. This observation raises problems for any edge-detector theory of vision, because there was no adaptation to edges. It was concluded that spatial-frequency mechanisms are operating at both low- and high-spatial frequencies and that an edge mechanism is operative at lower frequencies. The implications of these results are assessed for other theories of spatial vision.

Adaptation, Ocular

Spatial summation in young and elderly observers.

We measured detection thresholds for targets over a range of sizes at both photopic and scotopic luminance levels in young and elderly observers, and used these data to estimate spatial summation areas 10 degrees in the retinal periphery. There were differences in detection thresholds between the young and old groups at photopic and scotopic luminances, but no differences in spatial summation areas at either background luminance level.

Adult

Infant response to stimuli of similar hue and dissimilar shape: tracing the origins of the categorization of objects by hue.

This study confirms that infants, like older children, are capable of responding "categorically" to stimuli of different shape if these are similar in hue. 24 infants (mean age 20.0 weeks) were familiarized to a stimulus in 1 hue (dominant wavelength 515 nm) and in either of 2 different shapes (face of a bear or a rabbit) and then presented with 4 main test comparisons in which the familiar stimulus was paired with a novel stimulus in either the familiar or the alternate (novel) shape and in a novel hue from the same or a different category (dominant wavelengths being 548 and 482 nm, respectively, and equally different from the familiar hue). Infants displayed a preference for the novel stimuli only in the new-category hue. Control tasks with a further 40 infants (same mean age as experimental group) eliminated alternative explanations of this pattern of response in terms of differential brightness of the hues, hue preferences, or inability to discriminate the shapes.

Attention

Age-related changes in contrast sensitivity in central and peripheral retina.

Eight young (average age 20.4 years) and eight elderly (average age 64.4 years) observers took part in three experiments designed to study age-related changes in peripheral retinal function. A further eight young (average age 22.3 years) and eight elderly (average age 63.8 years) observers took part in a replication of experiment 3. All observers had normal or better-than-normal visual acuity and no evidence of ocular pathology. All testing was monocular and the eye with better visual acuity was used. In the first experiment contrast sensitivity was measured in central retina and 10 deg temporally, at spatial frequencies of 0.2, 0.8, 2.0, and 5.0 cycles deg-1. Young observers had better contrast sensitivities than older observers, but only at higher spatial frequencies (2.0 and 5.0 cycles deg-1). For both groups, contrast sensitivity was poorer with peripheral presentation of stimuli than with central presentation, but not for the lowest spatial frequency used (0.2 cycle deg-1). In the second experiment observers had to detect the presence of a sharp edge (square-wave luminance profile), while in the third and fourth experiments the target was a "fuzzy' edge (sine-wave profile). Edges were again presented centrally or 10 deg temporally. As expected from the data of experiment 1, young observers were better able to detect the sharp edge than were the older observers in both central and peripheral viewing conditions. For both age groups, edge detection was better during central viewing than during peripheral viewing. However, contrary to expectations based on the results of experiment 1, detection of the fuzzy edge was better for central than for peripheral viewing for both age groups in experiments 3 and 4. The apparent (and expected) equality of performance found in experiment 3 for young and elderly observers in detecting the fuzzy edge was shown to be due to the range of contrast values used. When appropriate contrast values were used in experiment 4, young observers detected fuzzy edges presented in central retina better than did elderly observers. The results of experiment 1 show sparing of the ability to process low spatial frequencies across (i) age and (ii) retinal location, and are discussed in terms of the notion of (i) models of age-related loss of visual function and (ii) cortical magnification. The results of experiments 2, 3, and 4 provide some support for the proposition that the contrast sensitivity of observers may be used to predict their performance on other visual tasks.(ABSTRACT TRUNCATED AT 400 WORDS)

Aging

On the spatial distribution of visual attention.

An implication of the data analysis and presentation of Podgorny and Shepard (1983) is that subjects are able to attend simultaneously to more than one square of a grid display when the squares are separated by unattended areas: Attention to such nonunitary areas produces similar benefits as attention to unitary areas. These benefits are reflected in reaction times (RTs), which were reported by Podgorny and Shepard (1983) as being related to a measure of spatial dispersion (compactness) of the attended areas, but this measure does not signify whether these areas are unitary or not. A reanalysis of part of Podgorny and Shepard's (1983) data shows that RTs to attended and unattended squares are almost identical when the attended areas are nonunitary. This reanalysis also shows that RTs are related to compactness for unitary attended areas but that this relation breaks down when attention is focused on nonunitary areas. In addition, Podgorny and Shepard's (1983) data are presented in a way that demonstrates the importance of the actual grid location of probes on RTs. The failure of compactness to reflect these aspects of the spatial nature of attention suggests that this metric is deficient when applied to the study of the spatial determinants of attention.

Attention

The sensitivity of binocular rivalry suppression to changes in orientation assessed by reaction-time and forced-choice techniques.

Binocular rivalry was induced between two orthogonal square-wave gratings of the same spatial frequency, luminance, contrast, and field size, presented dichoptically. One of the gratings could be instantly replaced by a third grating differing only in orientation. In one experiment subjects were required to respond as soon as an orientation change was noticed, and to withhold response to catch trials (no orientation change). When orientation changes were made to the visible grating, reaction time was found to be a U-shaped function of the magnitude of orientation change. When orientation changes were made to the grating undergoing binocular-rivalry suppression, an overall increase in reaction time was found with the increase being greater for large orientation changes (an asymmetrical U-shaped function). In another experiment subjects were required to detect the direction of a change in orientation in a two-alternative forced-choice procedure. Thresholds were thus obtained for 75% correct performance. It was found that thresholds for orientation changes made to the visible and invisible fields were identical from 20 degrees to 70 degrees orientation change. Outside this range thresholds were higher when orientation changes were made to the field suppressed by binocular rivalry. It is argued that the orientation functions obtained in the two experiments may represent incomplete suppression of either form or transient information during binocular rivalry.

Adaptation, Ocular

Interference effects in recalling movements.

In two experiments, the interaction of location and distance cues in the recall of pre-selected movements was investigated. In Expt 1, separate groups of subjects were required to remember either ther terminal location of, or the distance moved during, a criterion movement pre-selected within a 30 cm response region. Following either a 5 s or 30 s unfilled retention interval, subjects were required to recall the criterion movement using the particular movement cue (i.e. location or distance) in question. In Expt 2, a similar procedure was used, except that recall of the criterion movement followed either a 5 s or a 20 s unfilled, or a 20 s filled (backward counting) retention interval. Systematic manipulation of both the direction and magnitude of the starting position for recall movements revealed the subjects were unable to make the movement uninfluenced by the "unattended' movement cue. The interfering effect of this irrelevant cue was independent of the ongoing activity during the retention interval. The results suggest that memory for preselected movements is based on a combination of the two movement cues generated during production of the criterion movement.

Cues