scholarly journals Neural responses to natural visual motion are spatially selective across the visual field, with selectivity differing across brain areas and task

2021 ◽  
Author(s):  
Jason J Ki ◽  
Jacek P Dmochowski ◽  
Jonathan Touryan ◽  
Lucas C Parra

AbstractIt is well established that neural responses to visual stimuli are enhanced at select locations in the visual field. While spatial selectivity and the effects of spatial attention are well-understood for discrete tasks (e.g., visual cueing paradigms), little is known about neural response during a naturalistic visual experience that involves complex dynamic visual stimuli, for instance, driving. In this study, we assess the strength of neural responses across the visual space during a kart race video game. Specifically, we measure the correlation strength of scalp evoked potentials with optical flow magnitude at individual locations on the screen. We find the strongest neural responses for task-relevant locations in visual space, selectively extending to areas beyond the focus of overt attention: while the driver’s gaze is directed upon the heading direction at the center of the screen, we observe robust neural evoked responses also to peripheral areas such as the road and surrounding buildings. Importantly, this spatial selectivity of neural responses differs across scalp locations. Moreover, during active gameplay, the strength of the spatially-selective neural responses are enhanced compared to passive viewing. Spatially selective neural gains have previously been interpreted as an attentional gain mechanism. In this view, the present data suggest that different brain areas focus attention on different task-relevant portions of the visual field, reaching beyond the focus of overt attention.

Author(s):  
Sofia Russo ◽  
Giulia Calignano ◽  
Marco Dispaldro ◽  
Eloisa Valenza

Efficiency in the early ability to switch attention toward competing visual stimuli (spatial attention) may be linked to future ability to detect rapid acoustic changes in linguistic stimuli (temporal attention). To test this hypothesis, we compared individual performances in the same cohort of Italian-learning infants in two separate tasks: (i) an overlap task, measuring disengagement efficiency for visual stimuli at 4 months (Experiment 1), and (ii) an auditory discrimination task for trochaic syllabic sequences at 7 months (Experiment 2). Our results indicate that an infant’s efficiency in processing competing information in the visual field (i.e., visuospatial attention; Exp. 1) correlates with the subsequent ability to orient temporal attention toward relevant acoustic changes in the speech signal (i.e., temporal attention; Exp. 2). These results point out the involvement of domain-general attentional processes (not specific to language or the sensorial domain) playing a pivotal role in the development of early language skills in infancy.


1997 ◽  
Vol 4 (4) ◽  
pp. 318-327 ◽  
Author(s):  
R Wolf ◽  
M Heisenberg
Keyword(s):  

2006 ◽  
Vol 95 (6) ◽  
pp. 3712-3726 ◽  
Author(s):  
Frédéric V. Barthélemy ◽  
Ivo Vanzetta ◽  
Guillaume S. Masson

Visual neurons integrate information over a finite part of the visual field with high selectivity. This classical receptive field is modulated by peripheral inputs that play a role in both neuronal response normalization and contextual modulations. However, the consequences of these properties for visuomotor transformations are yet incompletely understood. To explore those, we recorded short-latency ocular following responses in humans to large center-only and center-surround stimuli. We found that eye movements are triggered by a mechanism that integrates motion over a restricted portion of the visual field, the size of which depends on stimulus contrast and increases as a function of time after response onset. We also found evidence for a strong nonisodirectional center-surround organization, responsible for normalizing the central, driving input so that motor responses are set to their most linear contrast dynamics. Such response normalization is delayed about 20 ms relative to tracking onset, gradually builds up over time, and is partly tuned for surround orientation/direction. These results outline the spatiotemporal organization of a behavioral receptive field, which might reflect a linear integration among subpopulations of cortical visual motion detectors.


1988 ◽  
Vol 60 (3) ◽  
pp. 940-965 ◽  
Author(s):  
M. R. Dursteler ◽  
R. H. Wurtz

1. Previous experiments have shown that punctate chemical lesions within the middle temporal area (MT) of the superior temporal sulcus (STS) produce deficits in the initiation and maintenance of pursuit eye movements (10, 34). The present experiments were designed to test the effect of such chemical lesions in an area within the STS to which MT projects, the medial superior temporal area (MST). 2. We injected ibotenic acid into localized regions of MST, and we observed two deficits in pursuit eye movements, a retinotopic deficit and a directional deficit. 3. The retinotopic deficit in pursuit initiation was characterized by the monkey's inability to match eye speed to target speed or to adjust the amplitude of the saccade made to acquire the target to compensate for target motion. This deficit was related to the initiation of pursuit to targets moving in any direction in the visual field contralateral to the side of the brain with the lesion. This deficit was similar to the deficit we found following damage to extrafoveal MT except that the affected area of the visual field frequently extended throughout the entire contralateral visual field tested. 4. The directional deficit in pursuit maintenance was characterized by a failure to match eye speed to target speed once the fovea had been brought near the moving target. This deficit occurred only when the target was moving toward the side of the lesion, regardless of whether the target began to move in the ipsilateral or contralateral visual field. There was no deficit in the amplitude of saccades made to acquire the target, or in the amplitude of the catch-up saccades made to compensate for the slowed pursuit. The directional deficit is similar to the one we described previously following chemical lesions of the foveal representation in the STS. 5. Retinotopic deficits resulted from any of our injections in MST. Directional deficits resulted from lesions limited to subregions within MST, particularly lesions that invaded the floor of the STS and the posterior bank of the STS just lateral to MT. Extensive damage to the densely myelinated area of the anterior bank or to the posterior parietal area on the dorsal lip of the anterior bank produced minimal directional deficits. 6. We conclude that damage to visual motion processing in MST underlies the retinotopic pursuit deficit just as it does in MT. MST appears to be a sequential step in visual motion processing that occurs before all of the visual motion information is transmitted to the brainstem areas related to pursuit.(ABSTRACT TRUNCATED AT 400 WORDS)


2021 ◽  
Author(s):  
Miao Li ◽  
Bert Reynvoet ◽  
Bilge Sayim

Humans can estimate the number of visually displayed items without counting. This capacity of numerosity perception has often been attributed to a dedicated system to estimate numerosity, or alternatively to the exploitation of various stimulus features, such as density, convex hull, the size of items and occupancy area. The distribution of the presented items is usually not varied with eccentricity in the visual field. However, our visual fields are highly asymmetric, and to date, it is unclear how inhomogeneities of the visual field impact numerosity perception. Besides eccentricity, a pronounced asymmetry is the radial-tangential anisotropy. For example, in crowding, radially placed flankers interfere more strongly with target perception than tangentially placed flankers. Similarly, in redundancy masking, the number of perceived items in repeating patterns is reduced when the items are arranged radially but not when they are arranged tangentially. Here, we investigated whether numerosity perception is subject to the radial-tangential anisotropy of spatial vision to shed light on the underlying topology of numerosity perception. Observers were presented with varying numbers of discs and asked to report the perceived number. There were two conditions. Discs were predominantly arranged radially in the “radial” condition and tangentially in the “tangential” condition. Additionally, the spacing between discs was scaled with eccentricity. Physical properties, such as average eccentricity, average spacing, convex hull, and density were kept as similar as possible in the two conditions. Radial arrangements were expected to yield underestimation compared to tangential arrangements. Consistent with the hypothesis, numerosity estimates in the radial condition were lower compared to the tangential condition. Magnitudes of radial alignment (as well as predicted crowding strength) correlated with the observed numerosity estimates. Our results demonstrate a robust radial-tangential anisotropy, suggesting that the topology of spatial vision determines numerosity estimation. We suggest that asymmetries of spatial vision should be taken into account when investigating numerosity estimation.


2020 ◽  
Author(s):  
Zixuan Wang ◽  
Yuki Murai ◽  
David Whitney

AbstractPerceiving the positions of objects is a prerequisite for most other visual and visuomotor functions, but human perception of object position varies from one individual to the next. The source of these individual differences in perceived position and their perceptual consequences are unknown. Here, we tested whether idiosyncratic biases in the underlying representation of visual space propagate across different levels of visual processing. In Experiment 1, using a position matching task, we found stable, observer-specific compressions and expansions within local regions throughout the visual field. We then measured Vernier acuity (Experiment 2) and perceived size of objects (Experiment 3) across the visual field and found that individualized spatial distortions were closely associated with variations in both visual acuity and apparent object size. Our results reveal idiosyncratic biases in perceived position and size, originating from a heterogeneous spatial resolution that carries across the visual hierarchy.


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.


2008 ◽  
Vol 20 (6) ◽  
pp. 1094-1106 ◽  
Author(s):  
Maria Concetta Morrone ◽  
Andrea Guzzetta ◽  
Francesca Tinelli ◽  
Michela Tosetti ◽  
Michela Del Viva ◽  
...  

We report here two cases of two young diplegic patients with cystic periventricular leukomalacia who systematically, and with high sensitivity, perceive translational motion of a random-dot display in the opposite direction. The apparent inversion was specific for translation motion: Rotation and expansion motion were perceived correctly, with normal sensitivity. It was also specific for random-dot patterns, not occurring with gratings. For the one patient that we were able to test extensively, contrast sensitivity for static stimuli was normal, but was very low for direction discrimination at high spatial frequencies and all temporal frequencies. His optokinetic nystagmus movements were normal but he was unable to track a single translating target, indicating a perceptual origin of the tracking deficit. The severe deficit for motion perception was also evident in the seminatural situation of a driving simulation video game. The perceptual deficit for translational motion was reinforced by functional magnetic resonance imaging studies. Translational motion elicited no response in the MT complex, although it did produce a strong response in many visual areas when contrasted with blank stimuli. However, radial and rotational motion produced a normal pattern of activation in a subregion of the MT complex. These data reinforce the existent evidence for independent cortical processing for translational, and circular or radial flow motion, and further suggest that the two systems have different vulnerability and plasticity to prenatal damage. They also highlight the complexity of visual motion perception, and how the delicate balance of neural activity can lead to paradoxical effects such as consistent misperception of the direction of motion. We advance a possible explanation of a reduced spatial sampling of the motion stimuli and report a simple model that simulates well the experimental results.


Author(s):  
Tianyi Yan ◽  
Jinglong Wu

In humans, functional imaging studies have found a homolog of the macaque motion complex, MT+, which is suggested to contain both the middle temporal (MT) and medial superior temporal (MST) areas in the ascending limb of the inferior temporal sulcus. In the macaque, the motion-sensitive MT and MST areas are adjacent in the superior temporal sulcus. Electrophysiology has identified several motion-selective regions in the superior temporal sulcus (STS) of the macaque. Two of the best-studied areas include the MT and MST areas. The MT area has strong projections to the adjacent MST area and is typically subdivided into the dorsal (MSTd) and lateral (MSTl) subregions. While MT encodes the basic elements of motion, MST has higher-order motion-processing abilities and has been implicated in the perception of both object motion and self motion. The macaque MST area has been shown to have considerably larger receptive fields than the MT area. The receptive fields of MT cells typically extend only a few degrees into the ipsilateral visual field, while MST neurons have receptive fields that extend well into the ipsilateral visual field. This study tentatively identifies these subregions as the human homologs of the macaque MT and MST areas, respectively (Fig. 1). Putative human MT and MST areas were typically located on the posterior/ventral and anterior/dorsal banks of a dorsal/posterior limb of the inferior temporal sulcus. These locations are similar to their relative positions in the macaque superior temporal sulcus.


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