[Form-color preference in childhood visual perception].
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The games imitating a clinical pathology conference and a session of the therapeutical-control commission are an efficient method of student learning during the biopsy-sectional course. They favour activation of perception, form clinico-anatomical thinking, facilitate the learning of the diagnosis concept and the role of physicians of various profile (therapeutist, surgeon, pathologist, gynecologist, etc.).
Continuous surface boundaries, object shape, and global motion can be perceived from information that is fragmentary in both space and time. The authors report investigations indicating that accretion and deletion of texture is only 1 member of a broader class of element transformations that produce boundaries, shape, and motion, through spatiotemporal boundary formation (SBF). The authors report 4 experiments exploring SBF. The first 3 examine the class of transformations producing SBF, indicating that local element changes in color, orientation, or location are all effective. A 4th experiment examines temporal constraints on SBF. Integration of local element changes to produce boundaries, form, and global motion appears to be confined to a 165-ms window. Two classes of spatiotemporal integration models are considered; the relation between SBF and other cases of boundary interpolation are discussed.
Researchers and clinicians working with various adult populations have no practical, complete, reliable, and valid method of measuring the tactile and kinesthetic functions of their clients. This study gathers preliminary normative information on the performance of adults on the Southern California Kinesthesia and Tactile Tests. Fifty-one normal men and women with a mean age of 26 years were administered the Kinesthesia, Manual Form Perception, Finger Indentification, Graphesthesia, Localization of Tactile Stimuli, and Double Tactile Stimuli Tests in the order in which they were standardized. Test-retest reliability was studied in 41 of these subjects. Results indicated that the assessment of normal adults was hampered by ceiling effects and by low reliability, but that these six tests might well serve a useful function in discriminating between relatively severe dysfunction and normal function in adults. Suggestions were made toward the development of new measurement instruments specifically designed for adults.
A neural network model is developed to explain how visual thalamocortical interactions give rise to boundary percepts such as illusory contours and surface percepts such as filled-in brightnesses. Top-down feedback interactions are needed in addition to bottom-up feed-forward interactions to simulate these data. One feedback loop is modeled between lateral geniculate nucleus (LGN) and cortical area V1, and another within cortical areas V1 and V2. The first feedback loop realizes a matching process which enhances LGN cell activities that are consistent with those of active cortical cells, and suppresses LGN activities that are not. This corticogeniculate feedback, being endstopped and oriented, also enhances LGN ON cell activations at the ends of thin dark lines, thereby leading to enhanced cortical brightness percepts when the lines group into closed illusory contours. The second feedback loop generates boundary representations, including illusory contours, that coherently bind distributed cortical features together. Brightness percepts form within the surface representations through a diffusive filling-in process that is contained by resistive gating signals from the boundary representations. The model is used to simulate illusory contours and surface brightness induced by Ehrenstein disks, Kanizsa squares, Glass patterns, and café wall patterns in single contrast, reverse contrast, and mixed contrast configurations. These examples illustrate how boundary and surface mechanisms can generate percepts that are highly context-sensitive, including how illusory contours can be amodally recognized without being seen, how model simple cells in V1 respond preferentially to luminance discontinuities using inputs from both LGN ON and OFF cells, how model bipole cells in V2 with two colinear receptive fields can help to complete curved illusory contours, how short-range simple cell groupings and long-range bipole cell groupings can sometimes generate different outcomes, and how model double-opponent, filling-in and boundary segmentation mechanisms in V4 interact to generate surface brightness percepts in which filling-in of enhanced brightness and darkness can occur before the net brightness distribution is computed by double-opponent interactions.
The large volumes of digital image data from radiological examinations demand further research and practical solutions in image compression before PACS solutions in large radiological departments are plausible. But another type of compression of image information is also possible, which has, in fact, been somewhat utilized already in analog form, but which has far better possibilities in the digital world. The number of essential images in dynamic X-ray, nuclear medicine, examinations etc. can be greatly reduced. These examinations producing image series are reviewed in terms of compression of information. 3-D displays are very useful in slice imaging, because they provide a means to see easier inside the human body than a number of slice images side by side. We also provide a new method, dynamic pulmonary imaging with digital fluoroscopy, as an example of the digital possibilities to compress a number of images into parametric images, numbers, histograms and curves. These processes also have other positive consequences information is transformed into a more easily perceptible form.
Stereoacuity was investigated in 3- to 5-year-old children and in adults by using four commercially available stereotests (the Frisby, Randot circles, Random-Dot E (RDE), and TNO tests) and by using an experimental stereotest. Comparative reanalysis was also made of data obtained from other studies of the RDE and Titmus circles tests. Stereoacuity norms are proposed for 3- to 5-year-old children for each of the commercially available tests. Factors influencing stereoacuity threshold differences among the different tests are discussed. The results on all tests are consistent with the hypothesis that binocular visual development is incomplete at 5 years of age.
Administered block designs that varied according to two parameters, Task Uncertainty and Perceptual Cohensiveness, to 83 persons 49 years of age or older. Performance was adjusted to remove motor speed differences. Performance changed significantly over the age span as a function of Task Uncertainty. From 49 years up, performance did not change as a function of Perceptual Cohesiveness. An analysis that included a group of 20 persons 30 years of age or younger yielded an interaction of Age and Perceptual Cohesiveness. From 49 years on, analytic or image segmentation processes do not seem to change, but other information processing becomes slower.
An elementary unit of visual pattern and form perception is thought to be the orientation of edges; this element has been studied extensively by neurophysiologists using oriented line segments or bars. These same stimuli have been used in the present study to measure threshold discriminations in cats before and after cortical lesions of areas 17 and/or 18. Control experiments showed that the discriminations were made by using a single cue, orientation, and that other stimulus parameters, width, length and contrast of the bar, were optimized. The extent of the lesions was evaluated anatomically from cell and fiber stained sections through cortex and thalamus, matched to retinotopic maps of Tusa et al. (Cortical Sensory Organization, Vol. 2, Humana Press, pp. 1-31, '81) and Sanderson (Journal of Comparative Neurology 143:101-118, '71), and physiologically from visual field position of receptive fields of cells recorded in areas neighboring the lesions. Lesions involving area 17 and large parts of area 18 produced a marked deficit in orientation discrimination which included a loss in retention, and after retraining a substantial increase in thresholds for up to 3 years when tested with long bars. There was no recovery of discrimination when the animals were tested with short bars. Lesions which involved area 17 plus small parts of 18, or lesions of areas 18 and 19, produced no retention deficit and resulted in an increase in thresholds only at low contrast and narrow width. These experiments revealed an excellent correlation between lesion locus and size and behavioral deficit. They indicate that the cortical representation of bar orientation used for discrimination is distributed within and across areas 17 and 18. The spread of the distribution depends on other stimulus parameters such as bar width and length. Furthermore the experiments show that neither the most narrowly tuned cells nor the X-cell system is required for fine orientation discrimination of a long bar.
Single neurons were recorded from the superficial layers of the superior colliculus of immobilized monkeys (Macaca mulatta and Macaca irus). Two main functional types of neurons were found. The neurons of the first type (Type I neurons) responded well to simple stationary and moving stimuli such as spots, bars or slits of light. The latency of their response was 41 +/- 6 ms. They were not directionally selective and responded to a large range of velocities. The neurons of the second type (Type II neurons) responded very poorly to simple visual stimuli and their activation required real objects or certain two-dimensional patterns. The mean latency of response of these units was 66 +/- 26 ms. Habituation was always present. Type II neurons were located in the lower part of the superficial layers. The characteristics of Type II neurons suggest that in the primate superior colliculus there is a mechanism that allows the recognition of the complexity and the novelty of a stimulus and guides orienting responses to those stimuli that are worth analyzing in detail.
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This article reports three experiments that deal with the source of the difficulty of Wason's (1977) THOG problem. The solution of this problem demands both the postulation of hypotheses and a combinatorial analysis of their consequences. Experiment 1 showed that the generation of the hypotheses is not in itself sufficient to solve the problem. Experiment 2 showed that a version presenting a plausible context for separating the level of data from that of hypotheses produced a better performance than both the original abstract version and a thematic version lacking the plausible context separating the levels. Experiment 3 gave evidence that this context can produce facilitation even with the geometric material of the classic version. This experiment also showed that a pictorial presentation of data and a verbal presentation of hypotheses affect performance negatively. The results demonstrate the role of problem representation in problem solving, and, in particular, the role of homogeneity in representing data and hypotheses in hypothetico-deductive reasoning.
Building on a simple model of a tectal column as the unit of processing in the amphibian tectum, we conduct a computer analysis of the interaction of a linear array of such columns. The model suggests that the inhibitory and excitatory activity in the tectum may have three functions: 1) spatio-temporal facilitation of column activity to a moving stimulus; 2) preference for the head of the stimulus, probably to avoid possible defensive reactions of the prey; and 3) modulating the state of excitation of the column once it has produced a response. The model also shows that the spatio-temporal effects of excitation and inhibition increases the acuity of the animal to the direction of the prey, through processes similar to lateral inhibition.
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