On Why Objects Appear Smaller in the Visual Periphery

2019 ◽  
Vol 31 (1) ◽  
pp. 88-96 ◽  
Author(s):  
Wladimir Kirsch ◽  
Roland Pfister ◽  
Wilfried Kunde
Keyword(s):  
Visual Field ◽  
Visual System ◽  
Structural Properties ◽  
Spatial Attention ◽  
Visuospatial Attention ◽  
Peripheral Target ◽  
Perceptual Distortion ◽  
Visual Periphery ◽  
Peripheral Location ◽  
Exogenous Cue

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.

Peripheral Movement, Induced Movement, and Aftereffects from Induced Movement

Perception ◽  
1981 ◽  
Vol 10 (2) ◽  
pp. 173-182 ◽  
Author(s):  
Anthony H Reinhardt-Rutland
Keyword(s):  
Visual Field ◽  
Visual System ◽  
Lateral Inhibition ◽  
Static Field ◽  
Relative Movement ◽  
Partial Explanation ◽  
Peripheral Location

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.

scholarly journals Stronger perceptual filling-in of spatiotemporal information in the blind spot compared to artificial gaps

2019 ◽  
Author(s):  
Yulia Revina ◽  
Gerrit W Maus
Keyword(s):  
Visual Field ◽  
Visual System ◽  
Visual Information ◽  
Blind Spot ◽  
Visual Input ◽  
Spatiotemporal Information ◽  
Peripheral Location

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.

Newborn's Preference for Faces

1996 ◽  
Vol 1 (3) ◽  
pp. 200-205 ◽  
Author(s):  
Carlo Umiltà ◽  
Francesca Simion ◽  
Eloisa Valenza
Keyword(s):  
Visual System ◽  
Structural Properties ◽  
Sensory Properties ◽  
Human Face ◽  
System Experiment ◽  
Face Experiment

Four experiments were aimed at elucidating some aspects of the preference for facelike patterns in newborns. Experiment 1 showed a preference for a stimulus whose components were located in the correct arrangement for a human face. Experiment 2 showed a preference for stimuli that had optimal sensory properties for the newborn visual system. Experiment 3 showed that babies directed their attention to a facelike pattern even when it was presented simultaneously with a non-facelike stimulus with optimal sensory properties. Experiment 4 showed the preference for facelike patterns in the temporal hemifield but not in the nasal hemifield. It was concluded that newborns' preference for facelike patterns reflects the activity of a subcortical system which is sensitive to the structural properties of the stimulus.

scholarly journals Vision as oculomotor reward: cognitive contributions to the dynamic control of saccadic eye movements

2021 ◽  
Author(s):  
Christian Wolf ◽  
Markus Lappe
Keyword(s):  
Eye Movements ◽  
Visual Field ◽  
Visual System ◽  
Dynamic Control ◽  
Saccadic Eye Movements ◽  
Saccade Target ◽  
Cognitive Mechanisms ◽  
Foveal Vision ◽  
Subsequent Behavior ◽  
High Level

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.

The visual system of a Palaeognathous bird: Visual field, retinal topography and retino-central connections in the Chilean Tinamou (Nothoprocta perdicaria)

2014 ◽  
Vol 523 (2) ◽  
pp. 226-250 ◽  
Author(s):  
Quirin Krabichler ◽  
Tomas Vega-Zuniga ◽  
Cristian Morales ◽  
Harald Luksch ◽  
Gonzalo J. Marín
Keyword(s):  
Visual Field ◽  
Visual System ◽  
Retinal Topography ◽  
Nothoprocta Perdicaria

Occipitoparietal alpha-band responses to the graded allocation of top-down spatial attention

2014 ◽  
Vol 112 (6) ◽  
pp. 1307-1316 ◽  
Author(s):  
Isabel Dombrowe ◽  
Claus C. Hilgetag
Keyword(s):  
Visual Field ◽  
Spatial Attention ◽  
Brain Regions ◽  
Alpha Band ◽  
Top Down ◽  
Attentional Resources ◽  
Parietal Lobes ◽  
Visual Spatial ◽  
Entire Visual Field ◽  
Band Activity

The voluntary, top-down allocation of visual spatial attention has been linked to changes in the alpha-band of the electroencephalogram (EEG) signal measured over occipital and parietal lobes. In the present study, we investigated how occipitoparietal alpha-band activity changes when people allocate their attentional resources in a graded fashion across the visual field. We asked participants to either completely shift their attention into one hemifield, to balance their attention equally across the entire visual field, or to attribute more attention to one-half of the visual field than to the other. As expected, we found that alpha-band amplitudes decreased stronger contralaterally than ipsilaterally to the attended side when attention was shifted completely. Alpha-band amplitudes decreased bilaterally when attention was balanced equally across the visual field. However, when participants allocated more attentional resources to one-half of the visual field, this was not reflected in the alpha-band amplitudes, which just decreased bilaterally. We found that the performance of the participants was more strongly reflected in the coherence between frontal and occipitoparietal brain regions. We conclude that low alpha-band amplitudes seem to be necessary for stimulus detection. Furthermore, complete shifts of attention are directly reflected in the lateralization of alpha-band amplitudes. In the present study, a gradual allocation of visual attention across the visual field was only indirectly reflected in the alpha-band activity over occipital and parietal cortexes.

scholarly journals Sign language experience redistributes attentional resources to the inferior visual field

2019 ◽  
Author(s):  
Chloé Stoll ◽  
Matthew William Geoffrey Dye
Keyword(s):  
Visual Field ◽  
Visual Attention ◽  
Visual System ◽  
Visual Fields ◽  
The Body ◽  
Language Experience ◽  
Bayesian Hierarchical ◽  
Signed Languages ◽  
Covert Visual Attention ◽  
Deaf Signers

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.

scholarly journals Cortical reorganization of the visual system in post-stroke hemianopia studied with fMRI

Stroke ◽  
2001 ◽  
Vol 32 (suppl_1) ◽  
pp. 334-334
Author(s):  
Gereon Nelles ◽  
Guido Widmann ◽  
Joachim Esser ◽  
Anette Meistrowitz ◽  
Johannes Weber ◽  
...  
Keyword(s):  
Visual Cortex ◽  
Visual Field ◽  
Visual System ◽  
Primary Visual Cortex ◽  
Visual Stimuli ◽  
Checkerboard Pattern ◽  
Partial Recovery ◽  
Area 18 ◽  
Area 19 ◽  
Stimulation Of

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.

Comparison at a Distance

Perception ◽  
10.1068/p3393 ◽  
2003 ◽  
Vol 32 (4) ◽  
pp. 395-414 ◽  
Author(s):  
Marina V Danilova ◽  
John D Mollon
Keyword(s):  
Visual Field ◽  
Spatial Frequency ◽  
Visual System ◽  
Spatial Separation ◽  
Orientation Discrimination ◽  
Human Observer ◽  
Systematic Effect ◽  
Trained Subjects ◽  
Stimulus Attribute ◽  
The Subject

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.

The Detection of Orientation of Small Objects

Perception ◽  
1997 ◽  
Vol 26 (1_suppl) ◽  
pp. 59-59
Author(s):  
J M Zanker ◽  
M P Davey
Keyword(s):  
Visual Field ◽  
Visual System ◽  
Computer Simulations ◽  
Visual Information ◽  
Human Performance ◽  
Receptive Fields ◽  
Experimental Result ◽  
Orientation Tuning ◽  
Basic Question ◽  
Visual Stream

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.

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