ODDITY PERFORMANCE IN RETARDATES. II. SIZE DISCRIMINATION FUNCTIONS FROM ODDITY AND VERBAL METHODS.
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1. Rats were maintained on a diet deficient in fat and on a normal diet of rat cubes. 2. Rats were trained to discriminate between vertical and horizontal striations. The minimal stripe width that could be used for discrimination was determined. 3. In bright illumination (0.7 or 4.5 ft.lamberts) both deficient and normal rats had the same ability to discriminate between black and white stripes. 4. With an illuminance of 0.002 ft.lambert, supplemented rats could discriminate as efficiently as at 0.7 ft.lambert, but deficient animals were unable to discriminate at 0.002 ft.lambert. 5. Control rats had 14% of docosahexaenoic acid in their retinal fats but the deficient rats had only 1%. 6. Deficient animals had no vitamin A stores in the liver whereas the control animals had about 190 i.u./g. 7. The visual acuity of the rats used was about 45' of arc.
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A simple stimulus generator has been constructed that permits a small illuminated target to be seen with variable inter-ocular disparity, when superimposed upon the binocular view of an outdoor landscape. This device was applied to several questions involving perception of size, distance and orientation, with the following results: (1) when the apparent distance to an "artificial moon", as perceived through stereopsis, is decreased by about 50-fold (from near horizon to about 60 m), its apparent size is reduced by only a miniscule amount (8% on average); hence, the moon illusion is probably not due to compensation--conscious or subconscious--for its apparent distance; (2) those changes in apparent size known as convergence micropsia vary as a function of the visual surround; for a vergence change of 1 deg, greater perceived change in size of a small target arises when a landscape is seen nearby than with empty sky as surround; (3) when a target is shown somewhat above the horizon against an empty sky, it must be viewed with divergence of the visual axes (image positions for "hyper-infinite" distance), in order to be perceived as vertically above objects on the skyline; this effect implies a strong backward tilt to the apparent vertical and probably reflects an attempt to "null out" the perceptual consequences of the convergence that typically occurs during downward saccades.
We investigated temporal properties of vertical-size and horizontal-size disparity processing for slant perception. Subjects indicated perceived slants for a stereoscopic stimulus in which the two magnitudes of vertical-size or horizontal-size disparities were oscillated stepwise with various frequencies (from 0.2 to 10 Hz). For the stimulus with vertical-size disparity oscillation, two slants corresponding to the two magnitudes of disparity were perceived for low-frequency conditions, whereas only a static mean slant of the two slants was perceived for high frequencies (5 and 10 Hz). For the stimulus with horizontal-size disparity oscillation, two slants were perceived for all the temporal frequency conditions. These results indicate that temporal properties of vertical- and horizontal-size disparity processing are clearly different and vertical-size disparities are temporally integrated over a period of around 500 ms for slant perception.
The effects of the size and eccentricity of the visual stimulus upon visually induced perception of self-motion (vection) were examined with various sizes of central and peripheral visual stimulation. Analysis indicated the strength of vection increased linearly with the size of the area in which the moving pattern was presented, but there was no difference in vection strength between central and peripheral stimuli when stimulus sizes were the same. Thus, the effect of stimulus size is homogeneous across eccentricities in the visual field.
The present study tested the theory that inferotemporal cortex integrates 1) distance information transmitted via superior colliculus-pulvinar afferents, with 2) form information transmitted via striate-prestriate cortex afferents (Gross, 1973a, 1973b). Monkeys were trained to choose the larger of two objects, independent of distance, to obtain a reward. Based on the integration theory, the following predictions concerning this size constancy discrimination were made: 1) monkeys with pulvinar lesions, unable to code distance, should be impaired and adopt strategies based on retinal image size; and 2) monkeys with prestriate lesions, unable to code retinal image size, should be impaired and adopt strategies based on distance. Contrary to these predictions, pulvinar lesions produced no deficit; and although prestriate lesions did produce an impairment, it was due to a failure to code distance in assessing the true size of the object. Thus, monkeys with prestriate lesions consistently responded to retinal image size instead of object size. Replicating an earlier report (Humphrey and Weiskrantz, 1969), inferotemporal lesions also produced an impairment; however, errors made by monkeys with inferotemporal lesions were random and could not be attributed to any consistent strategy. All monkeys reacquired the discrimmination postoperatively, indicating that there are multiple mechanisms available to the brain-damaged animal for the perception of size constancy.
Calculations made using the data of Kruger and Polar [J. opt. Soc. Am. A2, 1832-1835 (1985); Vision Res. 26, 957-971 (1986); Vision Res. 27, 555-567 (1987)] show that for three of the four subjects they studied, size-change and blur cues do not interact linearly in the control of accommodation. A simple non-linear interaction model is shown to fit the data for all four subjects.
The purpose of the study was to develop a battery of tests for use in evaluation of intra- and intersensory development of young children. A battery of 15 tests (4 visual, 4 auditory, 4 tactile-kinesthetic, and 3 intersensory) was administered to 109 normally developing 6- and 8-year-old and 32 slowly developing or learning disabled children. Interdependence of test items within each intrasensory and the intersensory category was determined; intercorrelations ranged from .00 to .78. Reliability estimates were also determined. Face validity was claimed for each item. The effects of age or developmental level on test performance were established. Based upon the interdependence of the tests, reliability estimates, and the capacity of the tests to discriminate among groups classified according to age or developmental level, a battery of 10 intra- and intersensory tests was proposed. The battery has 3 tests of visual perception-visual memory, dynamic depth perception, and size discrimination; 3 tests of auditory perception-auditory discrimination, auditory memory of related syllables, and auditory sequential memory of numbers; 2 tests of tactile-kinesthetic perception-tactile integration and movement awareness; and 2 tests of intersensory integration-auditory-tactile intergration and auditory-visual integration.
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Photic responsiveness of cells in the medial bank of the lateral suprasylvian cortex (Clare-Bishop area) was studied using a three-dimensional visual stimulator that reproduced two visual cues (motion disparity and change in size) for perception of three-dimensional motion of a visual stimulus. About one third of them (48/148) were selectively responsive to motion disparity corresponding to approaching (AP cells, n = 30) or recessive motion (RC cells, N = 18), another half to motion of retinal images in the same direction between the two eyes corresponding to fronto-parallel motion (FP cells, n = 75), and the remaining cells were rather equally responsive to these types of stimuli (NS cells, n = 25). More than a half of the AP (19/30) or RC (11/18) cells were also responsive to increase or decrease in stimulus size, respectively, and they were optimally activated by a combination of the motion and size stimuli while relatively few FP and NS cells were sensitive to change in stimulus size. These findings indicate that the Clare-Bishop cells encode three-dimensional motion on the basis of photic responsiveness to the motion and size cues.
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We compared the role of the red-green, blue-yellow, and luminance post-receptoral mechanisms in the perception of density. The task requires the comparison of densities between two stimuli composed of oriented bandpass elements, pseudo-randomly scattered across an area of constant size. The perception of density differences was measured by a temporal 2AFC procedure for all pairs of mechanisms and for four possible densities. We found that stimuli of identical physical densities are not perceived equally: there is a consistent bias in favour of blue-yellow stimuli which are perceived as significantly more dense than red-green and achromatic stimuli. We considered three factors that could have differentially affected the density perception of blue-yellow stimuli: an increase in the perceived size of the individual blue-yellow elements, a perceived contrast difference, and the presence of local orientation cues. We found that the increased perceived density of the blue-yellow stimuli occurred despite the fact that there was no increase in perceived size of the individual elements, and remained despite corrections for the two other factors. We conclude that the significant increase in perceived density for the blue-yellow mechanism is a global effect, associated with a perceived colour 'melting' of the elements in the array. Our data were fitted with the occupancy model of Allik and Tuulmets (1991, Perception & Psychophysics 49 303-314) and we found that blue-yellow stimuli have a greater 'occupancy' than red-green or achromatic stimuli.
This study explored the relationship between 3 dimensions of organizational structure--centralization, formalization, and size--and perceptions of procedural and interactional fairness. Data from 11 organizations (N = 209) indicated that, as predicted, centralization was negatively related to perceptions of procedural fairness, and organizational size was negatively related to interactional fairness. However, contrary to predictions, formalization was not related to perceptions of procedural fairness. Results suggest that organizational structure and design should play a more prominent role in our thinking about organizational fairness.
Human observers are unable to use disparity information to transform the angular velocity signal into a precise object-based code. The Weber fraction for discriminating changes in objective velocity (cm/sec) is about twice the Weber fraction for discriminating changes in angular velocity (deg/sec), and is substantially higher than predicted from a combination of the errors in judging disparity and angular velocity. By comparison, judgments of the distance traversed by the moving target show excellent size constancy. The discrimination of changes in objective size (cm) is as precise as the discrimination of changes in angular size (deg). The angular velocity signal is useful without transformation into an object-centered signal; it guides eye and body movements, and is the basis of motion parallax judgments. The need to retain this angular signal may explain why there is no efficient mechanism for velocity constancy.
Many subhuman species and human infants, children, and adults can use two-dimensional information of relative rate of angular-size change to anticipate collisions between the self and approaching objects or surfaces. But extant studies have not determined what information is used when subjects view simulated approach events providing two-dimensional information and three-dimensional information (distance and distance change), as well as lower-order visual information contained in real approach events. Three experiments suggest that, given these several possibilities, adults' judgments of collision time are best predicted by two-dimensional spatiotemporal values which are invariant over object sizes, distances traversed, approach velocities, and several lower-order variables such as absolute angular size. However, collision time is substantially underestimated, with absolute amount of underestimation increasing as a function of actual time-to-collision. Large constant errors and loss of judgment linearity beyond about 10 s to contact time suggest that current models of human performances based on use of time-to-collision information require modified assumptions of operator efficiency.
OBJECTIVE: To determine changes in intraperitoneal pressure (IPP) when dialysate fill volume is increased from 2.0 L to 2.5 L to 3.0 L per exchange, and to evaluate the relationship with subjective discomfort perception. DESIGN: Cross-sectional survey. SETTING: Seven Mexican hospital-based dialysis centers. PATIENTS: Eighty-one adult patients on continuous ambulatory peritoneal dialysis (CAPD) without restriction criteria for age, gender, or time on dialysis, were studied. Patients seropositive for HIV or hepatitis B, and those with cancer or receiving immunosuppressive drugs were excluded. Participants were studied as outpatients. MAIN MEASURES: Blindly and in random order, 2.0-, 2.5-, and 3.0-L volumes of dialysate were infused consecutively. Body surface area (BSA) was calculated from patient height and weight. IPP was assessed with the patient lying supine, measuring the height of the dialysate column inside the peritoneal dialysis bag tubing. Blood pressure and subjective discomfort perception (using a visual analog scale of 0-100 mm) were also evaluated and registered after each of the three exchanges. RESULTS: The IPP rose with each increase of dialysate volume and was higher in males than in females for each fill volume level. For males IPP was 18.9 +/- 6.9, 20.8 +/- 7.1, and 22.9 +/- 7.5 cm H2O; and for females it was 16.5 +/- 5.7, 18.4 +/- 5.5, and 19.7 +/- 6.2 cm H2O for 2.0-, 2.5-, and 3.0-L fill volumes respectively (p < 0.01 among fill volumes and between genders). Intraperitoneal pressure showed significant negative correlation with the fill volume corrected for patient body size as reflected by the dialysate volume/ BSA ratio (r= -0.393, p < 0.01; r= 0.319, p < 0.01; and r= -0.274, p < 0.02 for 2.0-, 2.5-, and 3.0-L fill volumes respectively). Discomfort score rose as fill volume rose, with a median of 0, 2.5, and 13.0 for 2.0-, 2.5-, and 3.0-L fill volumes respectively (p< 0.001). It is interesting, however, that with 2.5-L and 3.0-L dialysate infusion volumes, 64% and 44% of the patients, respectively, had no discomfort at all. CONCLUSION: Dialysate volume increase is associated with higher IPP, which is modulated by the gender and body size of the patients. Although the mean discomfort score was higher with larger dialysate volumes, there was no significant correlation between discomfort and IPP or the dialysate volume/BSA ratio. Many patients had no discomfort with 2.5-L or even with 3.0-L dialysate infusions; theoretically, they can be treated with larger volumes.
Three experiments on the effect of density and diameter on haptic perception of rod length are reported. In Experiment 1, the subjects wielded visually occluded rods of different densities. Perceived length was found to be affected by the density of the rod regardless of the actual length. In Experiment 2, three aluminum rods of different lengths with handles of four different diameters were wielded. Perceived length of the rod was found to be shorter as the diameter of the handle with which it was wielded increased. A diameter-length illusion was thereby produced. In Experiment 3, visually occluded rods of different diameters but of the same moment of inertia about the x-axis were wielded with the right hand, and tubes of different diameters were felt with the left hand. The subjects were instructed that their right hand was grasping a handle, and that the actual diameter of the rod could be felt with the left hand. Rods were perceived to be shorter if a larger diameter was felt with the left hand. The results showed that perceived length is not just a function of actual rod length, and that is not accounted for by inertia only. The results are discussed in terms of the nature of invariants and the effect of knowledge on perception.