Peripheral Movement, Induced Movement, and Aftereffects from Induced Movement

Perception ◽  
1981 ◽  
Vol 10 (2) ◽  
pp. 173-182 ◽  
Author(s):  
Anthony H Reinhardt-Rutland

Substantial rotatory induced movement and aftereffects associated with induced movement were observed in a large static patterned disc bounded at its periphery by a rotating patterned annulus. The area of the annulus was less than one tenth that of the disc, so its peripheral location seemed to be important in eliciting these phenomena. This was confirmed in two experiments comparing a peripheral annulus and a relatively central annulus in their ability to elicit induced movement and aftereffects in the same large static field. Aspects of the vection (induced self-movement) phenomenon may have been involved in generation of induced movement. This suggested that the motion-inducing properties of the peripheral annulus might have derived from: (i) its eccentric location in the perceiver's visual field; or (ii) its location with regard to the display itself. Two further experiments showed that (ii) was important for the elicitation of both induced movement and the aftereffects, and (i) was important for the elicitation of induced movement. Neurons responsive to relative movement in conjunction with lateral inhibition may provide a partial explanation for these effects. However, they do not explain why the visual system can assign considerable movement to a large static field under the conditions of these experiments.

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.


2006 ◽  
Vol 273 (1601) ◽  
pp. 2681-2686 ◽  
Author(s):  
Joshua A Solomon ◽  
Michael J Morgan

The human visual system exaggerates the difference between the tilts of adjacent lines or grating patches. In addition to this tilt illusion, we found that oblique flanks reduced acuity for small changes of tilt in the centre of the visual field. However, no flanks—regardless of their tilts—decreased sensitivity to contrast. Thus, the foveal tilt illusion should not be attributed to orientation-selective lateral inhibition. Nor is it similar to conventional crowding, which typically does not impair letter recognition in the fovea. Our observers behaved as though the reference orientation (horizontal) had a small tilt in the direction of the flanks. We suggest that the extent of this re-calibration varies randomly over trials, and we demonstrate that this stochastic re-calibration can explain flank-induced acuity loss in the fovea.


2019 ◽  
Author(s):  
Yulia Revina ◽  
Gerrit W Maus

Complete visual information about a scene and the objects within it is often not available to us. For example, objects may be partly occluded by other objects or have sections missing. In the retinal blind spot, there are no photoreceptors and visual input is not detected. However, due to perceptual filling-in by the visual system we often do not perceive these gaps. There is a lack of consensus on how much of the mechanism for perceptual filling-in is similar in the case of a natural scotoma like the blind spot and artificial scotomata such as sections of the stimulus being physically removed. Part of the difficulty in assessing this relationship arises from a lack of direct comparisons between the two cases, with artificial scotomata being tested in different locations in the visual field compared to the blind spot. The peripheral location of the blind spot may explain its enhanced filling-in compared to artificial scotomata, as reported in previous studies. In the present study, we directly compared perceptual filling-in of spatiotemporal information in the blind spot and artificial gaps of the same size and eccentricity. We found stronger perceptual filling-in in the blind spot, suggesting improved filling-in for the blind spot reported in previous studies cannot be simply attributed to its peripheral location.


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

1990 ◽  
Vol 149 (1) ◽  
pp. 281-292 ◽  
Author(s):  
D. Osorio ◽  
M. V. Srinivasan ◽  
R. B. Pinter

The orientation of freely walking flies (female Lucilia cuprina) to lines and stripes in a circular arena is described. The following observations were made. 1. The flies walked straight towards a dark line using the frontal eye region, but a pale line on a dark background was only weakly attractive. 2. In bright conditions flies walked in a curved line towards a black-white edge, the path being convex towards the dark side of the border. The curves indicated that the flies were heading for a point about 5–10 degrees to the dark side of the edge. 3. In dim conditions the edge of a dark region was not especially attractive and flies headed towards any point in the dark area. These observations can be accounted for by assuming that the fly walks towards the darkest region in its visual field (scototaxis). In bright conditions the edges of a dark region become more attractive than its centre. This change could be explained if lateral inhibition creates a ‘Mach-band’ effect, making the edges appear darker than the centre. Thus, fixation behaviour in walking Lucilia females seems to be a simple taxis.


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.


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