scholarly journals The constant color perception at various illuminations: Could the own cheek and nose permanently occurring on the periphery of observer's visual field provide the visual system with the necessary standard of spectral reflectance?

2010 ◽  
Vol 8 (17) ◽  
pp. 55-55
Author(s):  
V. Gavrik
2019 ◽  
Vol 31 (1) ◽  
pp. 88-96 ◽  
Author(s):  
Wladimir Kirsch ◽  
Roland Pfister ◽  
Wilfried Kunde

An object appears smaller in the periphery than in the center of the visual field. In two experiments ( N = 24), we demonstrated that visuospatial attention contributes substantially to this perceptual distortion. Participants judged the size of central and peripheral target objects after a transient, exogenous cue directed their attention to either the central or the peripheral location. Peripheral target objects were judged to be smaller following a central cue, whereas this effect disappeared completely when the peripheral target was cued. This outcome suggests that objects appear smaller in the visual periphery not only because of the structural properties of the visual system but also because of a lack of spatial attention.


Author(s):  
Christian Wolf ◽  
Markus Lappe

AbstractHumans and other primates are equipped with a foveated visual system. As a consequence, we reorient our fovea to objects and targets in the visual field that are conspicuous or that we consider relevant or worth looking at. These reorientations are achieved by means of saccadic eye movements. Where we saccade to depends on various low-level factors such as a targets’ luminance but also crucially on high-level factors like the expected reward or a targets’ relevance for perception and subsequent behavior. Here, we review recent findings how the control of saccadic eye movements is influenced by higher-level cognitive processes. We first describe the pathways by which cognitive contributions can influence the neural oculomotor circuit. Second, we summarize what saccade parameters reveal about cognitive mechanisms, particularly saccade latencies, saccade kinematics and changes in saccade gain. Finally, we review findings on what renders a saccade target valuable, as reflected in oculomotor behavior. We emphasize that foveal vision of the target after the saccade can constitute an internal reward for the visual system and that this is reflected in oculomotor dynamics that serve to quickly and accurately provide detailed foveal vision of relevant targets in the visual field.


2014 ◽  
Vol 523 (2) ◽  
pp. 226-250 ◽  
Author(s):  
Quirin Krabichler ◽  
Tomas Vega-Zuniga ◽  
Cristian Morales ◽  
Harald Luksch ◽  
Gonzalo J. Marín

2019 ◽  
Author(s):  
Chloé Stoll ◽  
Matthew William Geoffrey Dye

While a substantial body of work has suggested that deafness brings about an increased allocation of visual attention to the periphery there has been much less work on how using a signed language may also influence this attentional allocation. Signed languages are visual-gestural and produced using the body and perceived via the human visual system. Signers fixate upon the face of interlocutors and do not directly look at the hands moving in the inferior visual field. It is therefore reasonable to predict that signed languages require a redistribution of covert visual attention to the inferior visual field. Here we report a prospective and statistically powered assessment of the spatial distribution of attention to inferior and superior visual fields in signers – both deaf and hearing – in a visual search task. Using a Bayesian Hierarchical Drift Diffusion Model, we estimated decision making parameters for the superior and inferior visual field in deaf signers, hearing signers and hearing non-signers. Results indicated a greater attentional redistribution toward the inferior visual field in adult signers (both deaf and hearing) than in hearing sign-naïve adults. The effect was smaller for hearing signers than for deaf signers, suggestive of either a role for extent of exposure or greater plasticity of the visual system in the deaf. The data provide support for a process by which the demands of linguistic processing can influence the human attentional system.


Stroke ◽  
2001 ◽  
Vol 32 (suppl_1) ◽  
pp. 334-334
Author(s):  
Gereon Nelles ◽  
Guido Widmann ◽  
Joachim Esser ◽  
Anette Meistrowitz ◽  
Johannes Weber ◽  
...  

102 Introduction: Restitution of unilateral visual field defects following occipital cortex lesions occurs rarely. Partial recovery, however, can be observed in patients with incomplete lesion of the visual cortex. Our objective was to study the neuroplastic changes in the visual system that underlie such recovery. Methods and Results: Six patients with a left PCA-territory cortical stroke and 6 healthy control subjects were studied during rest and during visual stimulation using a 1.5 T fMRI with a 40 mT gradient. Visual stimuli were projected with a laptop computer onto a 154 x 115 cm screen, placed 90 cm in front of the gantry. Subjects were asked to fixate a red point in the center of the screen during both conditions. During stimulation, a black-and-white checkerboard pattern reversal was presented in each hemifield. For each side, 120 volumes of 48 contiguous axial fMRI images were obtained during rest and during hemifield stimulation in alternating order (60 volumes for each condition). Significant differences of rCBF between stimulation and rest were assessed as group analyses using statistical parametric mapping (SPM 99; p<0.01, corrected for multiple comparison). In controls, strong increases of rCBF (Z=7.6) occurred in the contralateral primary visual cortex V1 (area 17) and in V3a (area 18) and V5 (area 19). No differences were found between the right and left side in controls. During stimulation of the unaffected (left) visual field in hemianopic patients, activation occurred in contralateral V1, but the strongest increases of rCBF (Z>10) were seen in contralateral V3a (area 18) and V5 (area 19). During stimulation of the hemianopic (right) visual field, no activation was found in the primary visual cortex of either hemisphere. The most significant activation (Z=9.2) was seen in the ipsilateral V3a and V5 areas, and contralateral (left) V3a. Conclusions: Partial recovery from hemianopia is associated with strong ipsilateral activation of the visual system. Processing of visual stimuli in the hemianopic side spares the primary visual cortex and may involve recruitment of neurons in ipsilateral (contralesional) areas V3a and V5.


Perception ◽  
10.1068/p3393 ◽  
2003 ◽  
Vol 32 (4) ◽  
pp. 395-414 ◽  
Author(s):  
Marina V Danilova ◽  
John D Mollon

The visual system is known to contain hard-wired mechanisms that compare the values of a given stimulus attribute at adjacent positions in the visual field; but how are comparisons performed when the stimuli are not adjacent? We ask empirically how well a human observer can compare two stimuli that are separated in the visual field. For the stimulus attributes of spatial frequency, contrast, and orientation, we have measured discrimination thresholds as a function of the spatial separation of the discriminanda. The three attributes were studied in separate experiments, but in all cases the target stimuli were briefly presented Gabor patches. The Gabor patches lay on an imaginary circle, which was centred on the fixation point and had a radius of 5 deg of visual angle. Our psychophysical procedures were designed to ensure that the subject actively compared the two stimuli on each presentation, rather than referring just one stimulus to a stored template or criterion. For the cases of spatial frequency and contrast, there was no systematic effect of spatial separation up to 10 deg. We conclude that the subject's judgment does not depend on discontinuity detectors in the early visual system but on more central codes that represent the two stimuli individually. In the case of orientation discrimination, two naïve subjects performed as in the cases of spatial frequency and contrast; but two highly trained subjects showed a systematic increase of threshold with spatial separation, suggesting that they were exploiting a distal mechanism designed to detect the parallelism or non-parallelism of contours.


Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 59-59
Author(s):  
J M Zanker ◽  
M P Davey

Visual information processing in primate cortex is based on a highly ordered representation of the surrounding world. In addition to the retinotopic mapping of the visual field, systematic variations of the orientation tuning of neurons are described electrophysiologically for the first stages of the visual stream. On the way to understanding the relation of position and orientation representation, in order to give an adequate account of cortical architecture, it will be an essential step to define the minimum spatial requirements for detection of orientation. We addressed the basic question of spatial limits for detecting orientation by comparing computer simulations of simple orientation filters with psychophysical experiments in which the orientation of small lines had to be detected at various positions in the visual field. At sufficiently high contrast levels, the minimum physical length of a line whose orientation can just be resolved is not constant when presented at various eccentricities, but covaries inversely with the cortical magnification factor. A line needs to span less than 0.2 mm on the cortical surface in order to be recognised as oriented, independently of the actual eccentricity at which the stimulus is presented. This seems to indicate that human performance for this task approaches the physical limits, requiring hardly more than approximately three input elements to be activated, in order to detect the orientation of a highly visible line segment. Combined with the estimates for receptive field sizes of orientation-selective filters derived from computer simulations, this experimental result may nourish speculations of how the rather local elementary process underlying orientation detection in the human visual system can be assembled to form much larger receptive fields of the orientation-sensitive neurons known to exist in the primate visual system.


2000 ◽  
Vol 12 (6) ◽  
pp. 1001-1012 ◽  
Author(s):  
Erich Kasten ◽  
Dorothe A. Poggel ◽  
Bernhard A. Sabel

In a previously conducted randomized placebo-controlled trial, we were able to demonstrate significant visual field enlargement induced by restitution therapy in patients with cerebral lesions [Kasten, E., Wuest, S., Behrens-Bamann, W., & Sabel, B. A. (1998c). Computer-based training for the treatment of partial blindness. Nature Medicine, 4, 1083-1087.]. Visual field training was performed on a computer monitor for 1 hr per day over a period of 6 months. Since the procedure included only stimulation with white light, in the present study we investigated if this simple detection training had a transfer effect on color or form recognition in the trained area (i.e., in the absence of modality specific training). Answering this question would be crucial for planning optimal restitution therapy: In case there is no transfer of training effects to other visual modalities, a specific treatment of each visual function must be performed in order to achieve maximum benefit. Therefore, we analyzed the data from 32 patients with visual field defects who had participated in the original trial and whose form and color recognition had been investigated. The experimental group (n = 19, restitution training) experienced not only an increase of 12.8% correctly detected stimuli (PeriMa program, p < .05), but also an improvement of 5.6% in pattern recognition (PeriForm) and of 6.1% in color perception (PeriColor), respectively. In contrast, the placebo group (n = 13, fixation training) showed no significant changes from baseline to final outcome in any of the visual modalities (PeriMa: 0.3%; PeriForm: -0.3%; PeriColor: 0.4%). Conventional perimetry yielded an increase of 7.8% detected stimuli in the experimental group, but only of 1.2% in the placebo group (p < .05). For form recognition and color perception, the differences between the results of the experimental and the placebo groups narrowly missed significance. However, correlations of diagnostic results showed that mainly those patients who had achieved visual field enlargement also improved in color and form perception: r = .67 (p < .05) between PeriMa and PeriForm and r = .32 between PeriMa and PeriColor. We conclude that visual restitution training using a simple white light stimulus has at least some influence on improving other visual functions such as color and pattern recognition. This result supports the “bottleneck theory” of visual restitution, i.e., training effects can be explained as a process of perceptual learning and increased processing of information by residual structures surviving lesions of the primary visual pathways.


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