scholarly journals Task-specific, dimension-based attentional shaping of motion processing in area MT

2016 ◽  
Author(s):  
Bastian Schledde ◽  
F. Orlando Galashan ◽  
Magdalena Przybyla ◽  
Andreas K. Kreiter ◽  
Detlef Wegener
Keyword(s):  
Visual Processing ◽  
Visual Motion ◽  
Color Change ◽  
Visual Stimulation ◽  
Motion Processing ◽  
Specific Response ◽  
Area Mt ◽  
Temporal Area ◽  
Baseline Activity ◽  
Feature Dimension

AbstractNon-spatial selective attention is based on the notion that specific features or objects in the visual environment are effectively prioritized in cortical visual processing. Feature-based attention (FBA) in particular, is a well-studied process that dynamically and selectively enhances neurons preferentially processing the attended feature attribute (e.g. leftward motion). In everyday life, however, behavior may require high sensitivity for an entire feature dimension (e.g. motion). Yet, evidence for feature dimension-specific attentional modulation on a cellular level is lacking. We here investigate neuronal activity in macaque motion-selective medio-temporal area (MT) in an experimental setting requiring the monkeys to detect either a motion change or a color change. We hypothesized that neural activity in MT is enhanced if the task requires perceptual sensitivity to motion. Despite identical visual stimulation, we found that mean firing rates were higher in the motion task, and response variability and latency were lower as compared to the color task. This task-specific response modulation in the processing of visual motion was independent from the relation between attended and stimulating motion direction. It emerged already in the absence of visual input, and consisted of a spatially global and tuning-independent shift of the MT baseline activity. The results provide single cell support for the hypothesis of a feature dimension-specific top-down signal emphasizing the processing of an entire feature class.

scholarly journals Task-specific, dimension-based attentional shaping of motion processing in monkey area MT

2017 ◽  
Vol 118 (3) ◽  
pp. 1542-1555 ◽  
Author(s):  
Bastian Schledde ◽  
F. Orlando Galashan ◽  
Magdalena Przybyla ◽  
Andreas K. Kreiter ◽  
Detlef Wegener
Keyword(s):  
Visual Processing ◽  
Visual Information ◽  
Color Change ◽  
Visual Stimulation ◽  
Motion Processing ◽  
Motion Direction ◽  
Area Mt ◽  
Baseline Activity ◽  
Specific Dimension ◽  
Feature Dimension

Nonspatially selective attention is based on the notion that specific features or objects in the visual environment are effectively prioritized in cortical visual processing. Feature-based attention (FBA), in particular, is a well-studied process that dynamically and selectively addresses neurons preferentially processing the attended feature attribute (e.g., leftward motion). In everyday life, however, behavior may require high sensitivity for an entire feature dimension (e.g., motion), but experimental evidence for a feature dimension-specific attentional modulation on a cellular level is lacking. Therefore, we investigated neuronal activity in macaque motion-selective mediotemporal area (MT) in an experimental setting requiring the monkeys to detect either a motion change or a color change. We hypothesized that neural activity in MT is enhanced when the task requires perceptual sensitivity to motion. In line with this, we found that mean firing rates were higher in the motion task and that response variability and latency were lower compared with values in the color task, despite identical visual stimulation. This task-specific, dimension-based modulation of motion processing emerged already in the absence of visual input, was independent of the relation between the attended and stimulating motion direction, and was accompanied by a spatially global reduction of neuronal variability. The results provide single-cell support for the hypothesis of a feature dimension-specific top-down signal emphasizing the processing of an entire feature class. NEW & NOTEWORTHY Cortical processing serving visual perception prioritizes information according to current task requirements. We provide evidence in favor of a dimension-based attentional mechanism addressing all neurons that process visual information in the task-relevant feature domain. Behavioral tasks required monkeys to attend either color or motion, causing modulations of response strength, variability, latency, and baseline activity of motion-selective monkey area MT neurons irrespective of the attended motion direction but specific to the attended feature dimension.

scholarly journals Population Anisotropy in Area MT Explains a Perceptual Difference Between Near and Far Disparity Motion Segmentation

2011 ◽  
Vol 105 (1) ◽  
pp. 200-208 ◽  
Author(s):  
Finnegan J. Calabro ◽  
Lucia M. Vaina
Keyword(s):  
Visual Cues ◽  
Visual Motion ◽  
Population Distribution ◽  
Normal Population ◽  
Motion Processing ◽  
Area Mt ◽  
Temporal Area ◽  
Motion Discrimination ◽  
Mt Neurons ◽  
Simulated Performance

Segmentation of the visual scene into relevant object components is a fundamental process for successfully interacting with our surroundings. Many visual cues, including motion and binocular disparity, support segmentation, yet the mechanisms using these cues are unclear. We used a psychophysical motion discrimination task in which noise dots were displaced in depth to investigate the role of segmentation through disparity cues in visual motion stimuli ( experiment 1). We found a subtle, but significant, bias indicating that near disparity noise disrupted the segmentation of motion more than equidistant far disparity noise. A control experiment showed that the near-far difference could not be attributed to attention ( experiment 2). To account for the near-far bias, we constructed a biologically constrained model using recordings from neurons in the middle temporal area (MT) to simulate human observers' performance on experiment 1. Performance of the model of MT neurons showed a near-disparity skew similar to that shown by human observers. To isolate the cause of the skew, we simulated performance of a model containing units derived from properties of MT neurons, using phase-modulated Gabor disparity tuning. Using a skewed-normal population distribution of preferred disparities, the model reproduced the elevated motion discrimination thresholds for near-disparity noise, whereas a skewed-normal population of phases (creating individually asymmetric units) did not lead to any performance skew. Results from the model suggest that the properties of neurons in area MT are computationally sufficient to perform disparity segmentation during motion processing and produce similar disparity biases as those produced by human observers.

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)

Transient activity in monkey area MT represents speed changes and is correlated with human behavioral performance

2015 ◽  
Vol 113 (3) ◽  
pp. 890-903 ◽  
Author(s):  
Andreas Traschütz ◽  
Andreas K. Kreiter ◽  
Detlef Wegener
Keyword(s):  
Change Detection ◽  
Visual Stimulation ◽  
Threshold Model ◽  
Human Detection ◽  
Absolute Difference ◽  
Area Mt ◽  
Temporal Area ◽  
Wide Range ◽  
Speed Change ◽  
Neuronal Representation

Neurons in the middle temporal area (MT) respond to motion onsets and speed changes with a transient-sustained firing pattern. The latency of the transient response has recently been shown to correlate with reaction time in a speed change detection task, but it is not known how the sign, the amplitude, and the latency of this response depend on the sign and the magnitude of a speed change, and whether these transients can be decoded to explain speed change detection behavior. To investigate this issue, we measured the neuronal representation of a wide range of positive and negative speed changes in area MT of fixating macaques and obtained three major findings. First, speed change transients not only reflect a neuron's absolute speed tuning but are shaped by an additional gain that scales the tuned response according to the magnitude of a relative speed change. Second, by means of a threshold model positive and negative population transients of a moderate number of MT neurons explain detection of both positive and negative speed changes, respectively, at a level comparable to human detection rates under identical visual stimulation. Third, like reaction times in a psychophysical model of velocity detection, speed change response latencies follow a power-law function of the absolute difference of a speed change. Both this neuronal representation and its close correlation with behavioral measures of speed change detection suggest that neuronal transients in area MT facilitate the detection of rapid changes in visual input.

A Selective History of the Study of Visual Motion Aftereffects

Perception ◽  
1994 ◽  
Vol 23 (10) ◽  
pp. 1111-1134 ◽  
Author(s):  
Nicholas J Wade
Keyword(s):  
Visual Processing ◽  
Visual Motion ◽  
Motion Aftereffect ◽  
Theoretical Research ◽  
Motion Processing ◽  
Visual Science ◽  
Stationary Objects ◽  
Major Review ◽  
Cortical Visual Processing ◽  
Motion Aftereffects

The visual motion aftereffect (MAE) was initially described after observation of movements in the natural environment, like those seen in rivers and waterfalls: stationary objects appeared to move briefly in the opposite direction. In the second half of the nineteenth century the MAE was displaced into the laboratory for experimental enquiry with the aid of Plateau's spiral. Such was the interest in the phenomenon that a major review of empirical and theoretical research was written in 1911. In the latter half of the present century novel stimuli (like drifting gratings, isoluminance patterns, spatial and luminance ramps, random-dot kinematograms, and first-order and second-order motions), introduced to study space and motion perception generally, have been applied to examine MAEs. Developing theories of cortical visual processing have drawn upon MAEs to provide a link between psychophysics and physiology; this has been most pronounced in the context of monocular and binocular channels in the visual system, the combination of colour and contour information, and in the cortical sites most associated with motion processing. The relatively unchanging characteristic of the study of MAEs has been the mode of measurement: duration continues to be used as an index of its strength, although measures of threshold elevation and nulling with computer-generated motions are becoming more prevalent. The MAE is a part of the armoury of motion phenomena employed to uncover the mysteries of vision. Over the last 150 years it has proved itself immensely adaptable to the shifts of fashion in visual science, and it is likely to continue in this vein.

Ventral intraparietal area of the macaque: anatomic location and visual response properties

1993 ◽  
Vol 69 (3) ◽  
pp. 902-914 ◽  
Author(s):  
C. L. Colby ◽  
J. R. Duhamel ◽  
M. E. Goldberg
Keyword(s):  
Visual Motion ◽  
Visual Response ◽  
Intraparietal Sulcus ◽  
Stimulus Motion ◽  
Area Mt ◽  
Temporal Area ◽  
Response Properties ◽  
Preferred Direction ◽  
The Face ◽  
Ventral Intraparietal Area

1. The middle temporal area (MT) projects to the intraparietal sulcus in the macaque monkey. We describe here a discrete area in the depths of the intraparietal sulcus containing neurons with response properties similar to those reported for area MT. We call this area the physiologically defined ventral intraparietal area, or VIP. In the present study we recorded from single neurons in VIP of alert monkeys and studied their visual and oculomotor response properties. 2. Area VIP has a high degree of selectivity for the direction of a moving stimulus. In our sample 72/88 (80%) neurons responded at least twice as well to a stimulus moving in the preferred direction compared with a stimulus moving in the null direction. The average response to stimuli moving in the preferred direction was 9.5 times as strong as the response to stimuli moving in the opposite direction, as compared with 10.9 times as strong for neurons in area MT. 3. Many neurons were also selective for speed of stimulus motion. Quantitative data from 25 neurons indicated that the distribution of preferred speeds ranged from 10 to 320 degrees/s. The degree of speed tuning was on average twice as broad as that reported for area MT. 4. Some neurons (22/41) were selective for the distance at which a stimulus was presented, preferring a stimulus of equivalent visual angle and luminance presented near (within 20 cm) or very near (within 5 cm) the face. These neurons maintained their preference for near stimuli when tested monocularly, suggesting that visual cues other than disparity can support this response. These neurons typically could not be driven by small spots presented on the tangent screen (at 57 cm). 5. Some VIP neurons responded best to a stimulus moving toward the animal. The absolute direction of visual motion was not as important for these cells as the trajectory of the stimulus: the best stimulus was one moving toward a particular point on the face from any direction. 6. VIP neurons were not active in relation to saccadic eye movements. Some neurons (10/17) were active during smooth pursuit of a small target. 7. The predominance of direction and speed selectivity in area VIP suggests that it, like other visual areas in the dorsal stream, may be involved in the analysis of visual motion.

scholarly journals Functional Properties of Neurons in Macaque Area V3

1997 ◽  
Vol 77 (4) ◽  
pp. 1906-1923 ◽  
Author(s):  
Karl R. Gegenfurtner ◽  
Daniel C. Kiper ◽  
Jonathan B. Levitt
Keyword(s):  
Functional Properties ◽  
Visual Processing ◽  
Significant Proportion ◽  
Large Degree ◽  
Visual Signals ◽  
Motion Processing ◽  
Temporal Area ◽  
Area V2 ◽  
Layer 4 ◽  
Contrast Thresholds

Gegenfurtner, Karl R., Daniel C. Kiper, and Jonathan B. Levitt. Functional properties of neurons in macaque area V3. J. Neurophysiol. 77: 1906–1923, 1997. We investigated the functional properties of neurons in extrastriate area V3. V3 receives inputs from both magno- and parvocellular pathways and has prominent projections to both the middle temporal area (area MT) and V4. It may therefore represent an important site for integration and transformation of visual signals. We recorded the activity of single units representing the central 10° in anesthetized, paralyzed macaque monkeys. We measured each cell's spatial, temporal, chromatic, and motion properties with the use of a variety of stimuli. Results were compared with measurements made in V2 neurons at similar eccentricities. Similar to area V2, most of the neurons in our sample (80%) were orientation selective, and the distribution of orientation bandwidths was similar to that found in V2. Neurons in V3 preferred lower spatial and higher temporal frequencies than V2 neurons. Contrast thresholds of V3 neurons were extremely low. Achromatic contrast sensitivity was much higher than in V2, and similar to that found in MT. About 40% of all neurons showed strong directional selectivity. We did not find strongly directional cells in layer 4 of V3, the layer in which the bulk of V1 and V2 inputs terminate. This property seems to be developed within area V3. An analysis of the responses of directionally selective cells to plaid patterns showed that in area V3, as in MT and unlike in V1 and V2, there exist cells sensitive to the motion of the plaid pattern rather than to that of the components. The exact proportion of cells classified as being selective to color depended to a large degree on the experiment and on the criteria used for classification. With the use of the same conditions as in a previous study of V2 cells, we found as many (54%) color-selective cells as in V2 (50%). Furthermore, the responses of V3 cells to colored sinusoidal gratings were well described by a linear combination of cone inputs. The two subpopulations of cells responsive to color and to motion overlapped to a large extent, and we found a significant proportion of cells that gave reliable and directional responses to drifting isoluminant gratings. Our results show that there is a significant interaction between color and motion processing in area V3, and that V3 cells exhibit the more complex motion properties typically observed at later stages of visual processing.

scholarly journals Response properties of MST parafoveal neurons during smooth pursuit adaptation

2016 ◽  
Vol 116 (1) ◽  
pp. 210-217 ◽  
Author(s):  
Seiji Ono ◽  
Michael J. Mustari
Keyword(s):  
Smooth Pursuit ◽  
Time Course ◽  
Visual Motion ◽  
Visual Stimulation ◽  
Critical Role ◽  
Visual Sensitivity ◽  
Large Field ◽  
Target Velocity ◽  
Visual Response ◽  
Temporal Area

Visual motion neurons in the posterior parietal cortex play a critical role in the guidance of smooth pursuit eye movements. Initial pursuit (open-loop period) is driven, in part, by visual motion signals from cortical areas, such as the medial superior temporal area (MST). The purpose of this study was to determine whether adaptation of initial pursuit gain arises because of altered visual sensitivity of neurons at the cortical level. It is well known that the visual motion response in MST is suppressed after exposure to a large-field visual motion stimulus, showing visual motion adaptation. One hypothesis is that foveal motion responses in MST are associated with smooth pursuit adaptation using a small target spot. We used a step-ramp tracking task with two steps of target velocity (double-step paradigm), which induces gain-down or gain-up adaptation. We found that after gain-down adaptation 58% of our MST visual neurons showed a significant decrease in firing rate. This was the case even though visual motion input (before the pursuit onset) from target motion was constant. Therefore, repetitive visual stimulation during the gain-down paradigm could lead to adaptive changes in the visual response. However, the time course of adaptation did not show a correlation between the visual response and pursuit behavior. These results indicate that the visual response in MST may not directly contribute to the adaptive change in pursuit initiation.

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.

scholarly journals Temporal Limits of Visual Motion Processing: Psychophysics and Neurophysiology

2018 ◽  
Author(s):  
Bart G. Borghuis ◽  
Duje Tadin ◽  
Martin J.M. Lankheet ◽  
Joseph S. Lappin ◽  
Wim A. van de Grind
Keyword(s):  
Time Scale ◽  
Visual Motion ◽  
Visual Stimulation ◽  
Ganglion Cells ◽  
Temporal Frequency ◽  
Human Motion ◽  
Optimal Time ◽  
Motion Processing ◽  
Motion Vision ◽  
Visual Motion Processing

Under optimal conditions, just 3–6 ms of visual stimulation suffices for humans to see motion. Motion perception on this time scale implies that the visual system under these conditions reliably encodes, transmits, and processes neural signals with near-millisecond precision. Motivated by in vitro evidence for high temporal precision of motion signals in the primate retina, we investigated how neuronal and perceptual limits of motion encoding relate. Specifically, we examined the correspondence between the time scale at which cat retinal ganglion cells in vivo represent motion information and temporal thresholds for human motion discrimination. The time scale for motion encoding by ganglion cells ranged from 4.6–91 ms, depended nonlinearly on temporal frequency but not on contrast. Human psychophysics revealed that minimal stimulus durations required for perceiving motion direction were similarly brief, 5.6–65 ms, similarly depended on temporal frequency but, above ~10%, not on contrast. Notably, physiological and psychophysical measurements corresponded closely throughout (r = 0.99), despite more than a 20-fold variation in both human thresholds and optimal time scales for motion encoding in the retina. These results demonstrate that neural circuits for motion vision in cortex can maintain and make use of the high temporal fidelity of the retinal output signals.

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