scholarly journals Comparing the influence of stimulus size and contrast on the perception of moving gratings and random dot patterns—A registered report protocol

PLoS ONE ◽  
2021 ◽  
Vol 16 (6) ◽  
pp. e0253067
Author(s):  
Benedict Wild ◽  
Stefan Treue
Keyword(s):  
Motion Perception ◽  
Visual Motion ◽  
Human Subjects ◽  
Motion Processing ◽  
Temporal Area ◽  
Middle Temporal ◽  
Processing Pipeline ◽  
Visual Motion Processing ◽  
Primate Brain ◽  
Random Dot Patterns

Modern accounts of visual motion processing in the primate brain emphasize a hierarchy of different regions within the dorsal visual pathway, especially primary visual cortex (V1) and the middle temporal area (MT). However, recent studies have called the idea of a processing pipeline with fixed contributions to motion perception from each area into doubt. Instead, the role that each area plays appears to depend on properties of the stimulus as well as perceptual history. We propose to test this hypothesis in human subjects by comparing motion perception of two commonly used stimulus types: drifting sinusoidal gratings (DSGs) and random dot patterns (RDPs). To avoid potential biases in our approach we are pre-registering our study. We will compare the effects of size and contrast levels on the perception of the direction of motion for DSGs and RDPs. In addition, based on intriguing results in a pilot study, we will also explore the effects of a post-stimulus mask. Our approach will offer valuable insights into how motion is processed by the visual system and guide further behavioral and neurophysiological research.

Pursuit and optokinetic deficits following chemical lesions of cortical areas MT and MST

1988 ◽  
Vol 60 (3) ◽  
pp. 940-965 ◽  
Author(s):  
M. R. Dursteler ◽  
R. H. Wurtz
Keyword(s):  
Eye Movements ◽  
Visual Field ◽  
Visual Motion ◽  
Ibotenic Acid ◽  
Motion Processing ◽  
Temporal Area ◽  
Target Speed ◽  
Pursuit Eye Movements ◽  
Medial Superior Temporal ◽  
Visual Motion Processing

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)

scholarly journals Motion Perception in the Common Marmoset

2019 ◽  
Vol 30 (4) ◽  
pp. 2659-2673
Author(s):  
Shaun L Cloherty ◽  
Jacob L Yates ◽  
Dina Graf ◽  
Gregory C DeAngelis ◽  
Jude F Mitchell
Keyword(s):  
Motion Perception ◽  
Visual Motion ◽  
Common Marmoset ◽  
Neural Population ◽  
Motion Processing ◽  
Motion Direction ◽  
Visual Motion Processing ◽  
Trade Offs ◽  
Population Codes ◽  
The Common

Abstract Visual motion processing is a well-established model system for studying neural population codes in primates. The common marmoset, a small new world primate, offers unparalleled opportunities to probe these population codes in key motion processing areas, such as cortical areas MT and MST, because these areas are accessible for imaging and recording at the cortical surface. However, little is currently known about the perceptual abilities of the marmoset. Here, we introduce a paradigm for studying motion perception in the marmoset and compare their psychophysical performance with human observers. We trained two marmosets to perform a motion estimation task in which they provided an analog report of their perceived direction of motion with an eye movement to a ring that surrounded the motion stimulus. Marmosets and humans exhibited similar trade-offs in speed versus accuracy: errors were larger and reaction times were longer as the strength of the motion signal was reduced. Reverse correlation on the temporal fluctuations in motion direction revealed that both species exhibited short integration windows; however, marmosets had substantially less nondecision time than humans. Our results provide the first quantification of motion perception in the marmoset and demonstrate several advantages to using analog estimation tasks.

Center-Surround Interactions in the Middle Temporal Visual Area of the Owl Monkey

2000 ◽  
Vol 84 (5) ◽  
pp. 2658-2669 ◽  
Author(s):  
Richard T. Born
Keyword(s):  
Visual Motion ◽  
Receptive Fields ◽  
Visual Area ◽  
Motion Processing ◽  
Wide Field ◽  
Local Motion ◽  
Middle Temporal ◽  
Visual Motion Processing ◽  
Owl Monkey ◽  
Motion Contrast

Microelectrode recording and 2-deoxyglucose (2dg) labeling were used to investigate center-surround interactions in the middle temporal visual area (MT) of the owl monkey. These techniques revealed columnar groups of neurons whose receptive fields had opposite types of center-surround interaction with respect to moving visual stimuli. In one type of column, neurons responded well to objects such as a single bar or spot but poorly to large textured stimuli such as random dots. This was often due to the fact that the receptive fields had antagonistic surrounds: surround motion in the same direction as that preferred by the center suppressed responses, thus rendering these neurons unresponsive to wide-field motion. In the second set of complementary, interdigitated columns, neuronal receptive fields had reinforcing surrounds and responded optimally to wide-field motion. This functional organization could not be accounted for by systematic differences in binocular disparity. Within both column types, neurons whose receptive fields exhibited center-surround interactions were found less frequently in the input layers compared with the other layers. Additional tests were done on single units to examine the nature of the center-surround interactions. The direction tuning of the surround was broader than that of the center, and the preferred direction, with respect to that of the center, tended to be either in the same or opposite direction and only rarely in orthogonal directions. Surround motion at various velocities modulated the overall responsiveness to centrally placed moving stimuli, but it did not produce shifts in the peaks of the center's tuning curves for either direction or speed. In layers 3B and 5 of the local motion processing columns, a number of neurons responded only to local motion contrast but did so over a region of the visual field that was much larger than the optimal stimulus size. The central feature of this receptive field type was the generalization of surround antagonism over retinotopic space—a property similar to other “complex” receptive fields described previously. The columnar organization of different types of center-surround interactions may reflect the initial segregation of visual motion information into wide-field and local motion contrast systems that serve complementary functions in visual motion processing. Such segregation appears to occur at later stages of the macaque motion processing stream, in the medial superior temporal area (MST), and has also been described in invertebrate visual systems where it appears to be involved in the important function of distinguishing background motion from object motion.

Motion Perception: From Detection to Interpretation

2018 ◽  
Vol 4 (1) ◽  
pp. 501-523 ◽  
Author(s):  
Shin'ya Nishida ◽  
Takahiro Kawabe ◽  
Masataka Sawayama ◽  
Taiki Fukiage
Keyword(s):  
Motion Perception ◽  
Visual Motion ◽  
Specular Reflection ◽  
Motion Vector ◽  
Motion Processing ◽  
Local Motion ◽  
Computational Framework ◽  
Motion Signal ◽  
Visual Motion Processing ◽  
Level Of Processing

Visual motion processing can be conceptually divided into two levels. In the lower level, local motion signals are detected by spatiotemporal-frequency-selective sensors and then integrated into a motion vector flow. Although the model based on V1-MT physiology provides a good computational framework for this level of processing, it needs to be updated to fully explain psychophysical findings about motion perception, including complex motion signal interactions in the spatiotemporal-frequency and space domains. In the higher level, the velocity map is interpreted. Although there are many motion interpretation processes, we highlight the recent progress in research on the perception of material (e.g., specular reflection, liquid viscosity) and on animacy perception. We then consider possible linking mechanisms of the two levels and propose intrinsic flow decomposition as the key problem. To provide insights into computational mechanisms of motion perception, in addition to psychophysics and neurosciences, we review machine vision studies seeking to solve similar problems.

scholarly journals Processing of object motion and self-motion in the lateral subdivision of the medial superior temporal area in macaques

2019 ◽  
Vol 121 (4) ◽  
pp. 1207-1221 ◽  
Author(s):  
Ryo Sasaki ◽  
Dora E. Angelaki ◽  
Gregory C. DeAngelis
Keyword(s):  
Visual Cues ◽  
Moving Objects ◽  
Visual Motion ◽  
Object Motion ◽  
Image Motion ◽  
Motion Processing ◽  
Temporal Area ◽  
Medial Superior Temporal ◽  
Visual Motion Processing ◽  
Self Motion

Multiple areas of macaque cortex are involved in visual motion processing, but their relative functional roles remain unclear. The medial superior temporal (MST) area is typically divided into lateral (MSTl) and dorsal (MSTd) subdivisions that are thought to be involved in processing object motion and self-motion, respectively. Whereas MSTd has been studied extensively with regard to processing visual and nonvisual self-motion cues, little is known about self-motion signals in MSTl, especially nonvisual signals. Moreover, little is known about how self-motion and object motion signals interact in MSTl and how this differs from interactions in MSTd. We compared the visual and vestibular heading tuning of neurons in MSTl and MSTd using identical stimuli. Our findings reveal that both visual and vestibular heading signals are weaker in MSTl than in MSTd, suggesting that MSTl is less well suited to participate in self-motion perception than MSTd. We also tested neurons in both areas with a variety of combinations of object motion and self-motion. Our findings reveal that vestibular signals improve the separability of coding of heading and object direction in both areas, albeit more strongly in MSTd due to the greater strength of vestibular signals. Based on a marginalization technique, population decoding reveals that heading and object direction can be more effectively dissociated from MSTd responses than MSTl responses. Our findings help to clarify the respective contributions that MSTl and MSTd make to processing of object motion and self-motion, although our conclusions may be somewhat specific to the multipart moving objects that we employed. NEW & NOTEWORTHY Retinal image motion reflects contributions from both the observer’s self-motion and the movement of objects in the environment. The neural mechanisms by which the brain dissociates self-motion and object motion remain unclear. This study provides the first systematic examination of how the lateral subdivision of area MST (MSTl) contributes to dissociating object motion and self-motion. We also examine, for the first time, how MSTl neurons represent translational self-motion based on both vestibular and visual cues.

Relation of cortical areas MT and MST to pursuit eye movements. I. Localization and visual properties of neurons

1988 ◽  
Vol 60 (2) ◽  
pp. 580-603 ◽  
Author(s):  
H. Komatsu ◽  
R. H. Wurtz
Keyword(s):  
Eye Movements ◽  
Smooth Pursuit ◽  
Visual Motion ◽  
Receptive Fields ◽  
Motion Processing ◽  
Temporal Area ◽  
Pursuit Eye Movements ◽  
Visual Motion Processing ◽  
Visual Areas ◽  
Visual Properties

1. Among the multiple extrastriate visual areas in monkey cerebral cortex, several areas within the superior temporal sulcus (STS) are selectively related to visual motion processing. In this series of experiments we have attempted to relate this visual motion processing at a neuronal level to a behavior that is dependent on such processing, the generation of smooth-pursuit eye movements. 2. We studied two visual areas within the STS, the middle temporal area (MT) and the medial superior temporal area (MST). For the purposes of this study, MT and MST were defined functionally as those areas within the STS having a high proportion of directionally selective neurons. MST was distinguished from MT by using the established relationship of receptive-field size to eccentricity, with MST having larger receptive fields than MT. 3. A subset of these visually responsive cells within the STS were identified as pursuit cells--those cells that discharge during smooth pursuit of a small target in an otherwise dark room. Pursuit cells were found only in localized regions--in the foveal region of MT (MTf), in a dorsal-medial area of MST on the anterior bank of the STS (MSTd), and in a lateral-anterior area of MST on the floor and the posterior bank of the STS (MST1). 4. Pursuit cells showed two characteristics in common when their visual properties were studied while the monkey was fixating. Almost all cells showed direction selectivity for moving stimuli and included the fovea within their receptive fields. 5. The visual response of pursuit cells in the several areas differed in two ways. Cells in MTf preferred small moving spots of light, whereas cells in MSTd preferred large moving stimuli, such as a pattern of random dots. Cells in MTf had small receptive fields; those in MSTd usually had large receptive fields. Visual responses of pursuit neurons in MST1 were heterogeneous; some resembled those in MTf, whereas others were similar to those in MSTd. This suggests that the pursuit cells in MSTd and MST1 belong to different subregions of MST.

scholarly journals White matter deficits correlate with visual motion perception impairments in dyslexic carriers of the DCDC2 genetic risk variant

2021 ◽  
Author(s):  
Daniela Perani ◽  
Paola Scifo ◽  
Guido M. Cicchini ◽  
Pasquale Della Rosa ◽  
Chiara Banfi ◽  
...  
Keyword(s):  
White Matter ◽  
Motion Perception ◽  
Visual Motion ◽  
Visual Analysis ◽  
Temporal Cortex ◽  
Inferior Temporal Cortex ◽  
Motion Processing ◽  
Motion Direction ◽  
Risk Variant ◽  
Visual Motion Processing

AbstractMotion perception deficits in dyslexia show a large intersubjective variability, partly reflecting genetic factors influencing brain architecture development. In previous work, we have demonstrated that dyslexic carriers of a mutation of the DCDC2 gene have a very strong impairment in motion perception. In the present study, we investigated structural white matter alterations associated with the poor motion perception in a cohort of twenty dyslexics with a subgroup carrying the DCDC2 gene deletion (DCDC2d+) and a subgroup without the risk variant (DCDC2d–). We observed significant deficits in motion contrast sensitivity and in motion direction discrimination accuracy at high contrast, stronger in the DCDC2d+ group. Both motion perception impairments correlated significantly with the fractional anisotropy in posterior ventral and dorsal tracts, including early visual pathways both along the optic radiation and in proximity of occipital cortex, MT and VWFA. However, the DCDC2d+ group showed stronger correlations between FA and motion perception impairments than the DCDC2d– group in early visual white matter bundles, including the optic radiations, and in ventral pathways located in the left inferior temporal cortex. Our results suggest that the DCDC2d+ group experiences higher vulnerability in visual motion processing even at early stages of visual analysis, which might represent a specific feature associated with the genotype and provide further neurobiological support to the visual-motion deficit account of dyslexia in a specific subpopulation.

Visual motion processing in the anterior ectosylvian sulcus of the cat

1996 ◽  
Vol 76 (2) ◽  
pp. 895-907 ◽  
Author(s):  
J. W. Scannell ◽  
F. Sengpiel ◽  
M. J. Tovee ◽  
P. J. Benson ◽  
C. Blakemore ◽  
...  
Keyword(s):  
Visual Area ◽  
Motion Processing ◽  
Published Data ◽  
Anterior Ectosylvian Sulcus ◽  
Temporal Area ◽  
Middle Temporal ◽  
Visual Motion Processing ◽  
Pattern Motion ◽  
Middle Temporal Area ◽  
Component Motion

1. Neurons that are selectively sensitive to the direction of motion of elongated contours have been found in several cortical areas in many species. However, in the striate cortex of the cat and monkey, and the extrastriate posteromedial lateral suprasylvian visual area of the cat, such cells are generally component motion selective, signaling only the direction of movement orthogonal to the preferred orientation; a direction that is not necessarily the same as the motion of the entire pattern or texture of which the cell's preferred contour is part. The primate extrastriate middle temporal area is the only cortical region currently known to contain a substantial population of pattern-motion-selective cells that respond to the shared vector of motion of mixtures of contours. 2. From analyzing published data on the connectivity of the cat's cortex, we predicted that the anterior ectosylvian visual area (AEV), situated within the anterior ectosylvian sulcus, might be a higher-order motion processing area and thus likely to contain pattern-motion-selective neurons. This paper presents the results of a study on neuronal responses in AEV. 3. Ninety percent of AEV cells that responded strongly to drifting grating and/or plaid stimuli were directionally selective (directionality index > 0.5). For this group, the mean directionality index was 0.75. Moreover, 55% of these cells were unequivocally classified as pattern motion selective and only one neuron was classified as definitely component motion selective. Thus high-level pattern motion coding occurs in the cat extrastriate cortex and is not limited to the primate middle temporal area. 4. AEV contains a heterogeneous population of directionally selective cells. There was no clear relation between the degree of directional selectivity for plaids or gratings and the degree of selectivity for pattern motion or component motion. Nevertheless, 28% of the highly responsive cells were both more strongly modulated by plaids than gratings and more pattern motion selective than component motion selective. Such cells could correspond to a population of "selection units" signaling the salience of local motion information. 5. AEV lacks global retinotopic order but the preferred direction of motion of neurons (rather than axis of motion, as in the middle temporal area and the posteromedial lateral suprasylvian visual area) is mapped systematically across the cortex. Our data are compatible with AEV being a nonretinotopic, feature-mapped area in which cells representing similar parts of "motion space" are brought together on the cortical sheet.

scholarly journals Motion perception in the common marmoset

2019 ◽  
Author(s):  
Shaun L. Cloherty ◽  
Jacob L. Yates ◽  
Dina Graf ◽  
Gregory C. DeAngelis ◽  
Jude F. Mitchell
Keyword(s):  
Motion Perception ◽  
Visual Motion ◽  
Common Marmoset ◽  
Neural Population ◽  
Motion Processing ◽  
Motion Direction ◽  
Visual Motion Processing ◽  
Trade Offs ◽  
Population Codes ◽  
The Common

AbstractVisual motion processing is a well-established model system for studying neural population codes in primates. The common marmoset, a small new world primate, offers unparalleled opportunities to probe these population codes in key motion processing areas, such as cortical areas MT and MST, because these areas are accessible for imaging and recording at the cortical surface. However, little is currently known about the perceptual abilities of the marmoset. Here, we introduce a paradigm for studying motion perception in the marmoset and compare their psychophysical performance to human observers. We trained two marmosets to perform a motion estimation task in which they provided an analog report of their perceived direction of motion with an eye movement to a ring that surrounded the motion stimulus. Marmosets and humans exhibited similar trade-offs in speed vs. accuracy: errors were larger and reaction times were longer as the strength of the motion signal was reduced. Reverse correlation on the temporal fluctuations in motion direction revealed that both species exhibited short integration windows, however, marmosets had substantially less non-decision time than humans. Our results provide the first quantification of motion perception in the marmoset and demonstrate several advantages to using analog estimation tasks.

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