Rapid Processing of Retinal Slip During Saccades in Macaque Area MT

2005 ◽  
Vol 94 (1) ◽  
pp. 235-246 ◽  
Author(s):  
N.S.C. Price ◽  
M. R. Ibbotson ◽  
S. Ono ◽  
M. J. Mustari
Keyword(s):  
Visual Motion ◽  
Single Cells ◽  
Direction Selectivity ◽  
Wide Field ◽  
Evoked Responses ◽  
Area Mt ◽  
Temporal Area ◽  
Retinal Slip ◽  
Passive Viewing ◽  
Direction Tuning

The primate middle temporal area (MT) is involved in the analysis and perception of visual motion, which is generated actively by eye and body movements and passively when objects move. We studied the responses of single cells in area MT of awake macaques, comparing the direction tuning and latencies of responses evoked by wide-field texture motion during fixation (passive viewing) and during rewarded, target-directed saccades and nonrewarded, spontaneous saccades over the same stationary texture (active viewing). We found that MT neurons have similar motion sensitivity and direction-selectivity for retinal slip associated with active and passive motion. No cells showed reversals in direction tuning between the active and passive viewing conditions. However, mean latencies were significantly different for saccade-evoked responses (30 ms) and stimulus-evoked responses (67 ms). Our results demonstrate that neurons in area MT retain their direction-selectivity and display reduced processing times during saccades. This rapid, accurate processing of peri-saccadic motion may facilitate postsaccadic ocular following reflexes or corrective saccades.

scholarly journals Properties of pattern and component direction-selective cells in area MT of the macaque

2016 ◽  
Vol 115 (6) ◽  
pp. 2705-2720 ◽  
Author(s):  
Helena X. Wang ◽  
J. Anthony Movshon
Keyword(s):  
Spatial Frequency ◽  
Visual Motion ◽  
Drift Rate ◽  
Receptive Fields ◽  
Direction Selectivity ◽  
Area Mt ◽  
Direction Tuning ◽  
Pattern Index ◽  
Component Direction ◽  
True Direction

Neurons in area MT/V5 of the macaque visual cortex encode visual motion. Some cells are selective for the motion of oriented features (component direction-selective, CDS); others respond to the true direction of complex patterns (pattern-direction selective, PDS). There is a continuum of selectivity in MT, with CDS cells at one extreme and PDS cells at the other; we compute a pattern index that captures this variation. It is unknown how a neuron's pattern index is related to its other tuning characteristics. We therefore analyzed the responses of 792 MT cells recorded in the course of other experiments from opiate-anesthetized macaque monkeys, as a function of the direction, spatial frequency, drift rate, size, and contrast of sinusoidal gratings and of the direction and speed of random-dot textures. We also compared MT responses to those of 718 V1 cells. As expected, MT cells with higher pattern index tended to have stronger direction selectivity and broader direction tuning to gratings, and they responded better to plaids than to gratings. Strongly PDS cells also tended to have smaller receptive fields and stronger surround suppression. Interestingly, they also responded preferentially to higher drift rates and higher speeds of moving dots. The spatial frequency preferences of PDS cells depended strongly on their preferred temporal frequencies, whereas these preferences were independent in component-selective cells. Pattern direction selectivity is statistically associated with many response properties of MT cells but not strongly associated with any particular property. Pattern-selective signals are thus available in association with most other signals exported by MT.

Area MT Neurons Respond to Visual Motion Distant From Their Receptive Fields

2005 ◽  
Vol 94 (6) ◽  
pp. 4156-4167 ◽  
Author(s):  
Daniel Zaksas ◽  
Tatiana Pasternak
Keyword(s):  
Time Course ◽  
Visual Motion ◽  
Cognitive Task ◽  
Receptive Fields ◽  
Direction Selectivity ◽  
Task Demands ◽  
Visual Signals ◽  
Area Mt ◽  
Mt Neurons ◽  
Stimulus Offset

Neurons in cortical area MT have localized receptive fields (RF) representing the contralateral hemifield and play an important role in processing visual motion. We recorded the activity of these neurons during a behavioral task in which two monkeys were required to discriminate and remember visual motion presented in the ipsilateral hemifield. During the task, the monkeys viewed two stimuli, sample and test, separated by a brief delay and reported whether they contained motion in the same or in opposite directions. Fifty to 70% of MT neurons were activated by the motion stimuli presented in the ipsilateral hemifield at locations far removed from their classical receptive fields. These responses were in the form of excitation or suppression and were delayed relative to conventional MT responses. Both excitatory and suppressive responses were direction selective, but the nature and the time course of their directionality differed from the conventional excitatory responses recorded with stimuli in the RF. Direction selectivity of the excitatory remote response was transient and early, whereas the suppressive response developed later and persisted after stimulus offset. The presence or absence of these unusual responses on error trials, as well as their magnitude, was affected by the behavioral significance of stimuli used in the task. We hypothesize that these responses represent top-down signals from brain region(s) accessing information about stimuli in the entire visual field and about the behavioral state of the animal. The recruitment of neurons in the opposite hemisphere during processing of behaviorally relevant visual signals reveals a mechanism by which sensory processing can be affected by cognitive task demands.

Reaction Time and Time Course of Neuronal Responses in MT and MST at Different Stimulus Contrasts

Perception ◽  
1996 ◽  
Vol 25 (1_suppl) ◽  
pp. 157-157 ◽  
Author(s):  
A Thiele ◽  
K-P Hoffmann
Keyword(s):  
Reaction Time ◽  
Single Cell ◽  
Single Cells ◽  
Direction Selectivity ◽  
Contrast Level ◽  
Population Activity ◽  
Temporal Area ◽  
Population Mean ◽  
The Mean ◽  
Mean Reaction Time

Direction-selective neurons from the middle temporal area (MT) and the middle superior temporal area (MST) were recorded while a monkey performed a direction discrimination task. Stimuli consisted of evenly spaced bars moving in one of the four cardinal directions. Monkey's reaction time, single-cell latency, and direction selectivity were calculated when stimuli of 53%, 24%, and 4% contrast were presented, and the monkey indicated a correct decision. Mean reaction time was 359±77 ms at 53% contrast, 391±107 ms at 24% contrast, and 582±374 ms at 4% contrast. Most neurons exhibiting direction selective responses at 53% contrast was also active at 24% contrast (MT, 99%; MST, 88%). The number of neurons still exhibiting stimulus-related activity at 4% contrast dramatically decreased (MT to 28%; MST to 41%). Shortest latencies were found at high contrast level (53% contrast; MT, 29 ms; population mean, 76±40 ms; MST, 35 ms; population mean, 77±27 ms). Single cell and population latency increased at lower contrast (4% contrast: MT minimum, 86 ms; population mean, 180±76 ms; MST minimum, 97 ms; population mean, 205±56 ms). This indicates that the mean increase in latency at the single-cell level only partially reflects the increase in reaction time (mean reaction time increased by 223 ms, while mean single-cell latency increased by ∼100 ms in MT and MST). We therefore calculated the normalised population response at different contrast levels. The maximal population activity was always found at the highest contrast level and this was set to 1. In MT it took 75 – 80 ms from stimulus onset until half maximal activity (0.5) was reached at 53% contrast. To reach 0.5 took 85 – 90 ms at 24% contrast and 205 – 210 ms at 4% contrast. For MST the respective values were 85 ms (53% contrast), 90 ms (24% contrast) and 255 ms (4%) contrast. Thus the time to reach half the maximal population activity much better reflects the reaction time than the mean of the latencies calculated from single cells.

Motion selectivity in macaque visual cortex. III. Psychophysics and physiology of apparent motion

1986 ◽  
Vol 55 (6) ◽  
pp. 1340-1351 ◽  
Author(s):  
W. T. Newsome ◽  
A. Mikami ◽  
R. H. Wurtz
Keyword(s):  
Apparent Motion ◽  
Cortical Neurons ◽  
Striate Cortex ◽  
Preceding Paper ◽  
Direction Selectivity ◽  
Physiological Data ◽  
Area Mt ◽  
Temporal Area ◽  
Psychophysical Data ◽  
Spatial Interval

We have conducted physiological and psychophysical experiments to identify possible neural substrates of the perception of apparent motion. We used identical sequences of flashed stimuli in both sets of experiments to better compare the responses of cortical neurons and psychophysical observers. Physiological data were obtained from two cortical visual areas, striate cortex (V1) and the middle temporal area (MT). In the previous paper we presented evidence that neuronal thresholds for direction selectivity in extrastriate area MT were similar to psychophysical thresholds for motion perception at the largest effective interflash interval, and thus speed, for a given eccentricity. We now examine physiological and psychophysical thresholds for a broad range of speeds to determine whether such a correspondence exists for speeds below the upper threshold considered in the previous paper. Stimuli were presented in stroboscopic motion of constant apparent speed while the spatial and temporal interflash intervals were systematically varied. For each neuron we measured the largest spatial interval that elicited directionally selective responses at each of several apparent speeds. We calculated the composite performance of neurons in both MT and V1 by averaging the spatial interval necessary for direction selectivity at each apparent speed. We employed the same apparent-motion stimuli for psychophysical experiments with human subjects in which we measured the spatial interval necessary for the perception of motion over a similar range of apparent speeds. We obtained a composite profile of psychophysical performance by averaging thresholds across subjects at each apparent speed. For high apparent speeds, physiological data from MT, but not V1, corresponded closely to the psychophysical data as suggested in the preceding paper. For low apparent speeds, however, physiological data from MT and V1 were similar to each other and to the psychophysical data. It would appear, therefore, that neurons in either V1 or MT could mediate the perceptual effect at low speeds, whereas MT is a stronger candidate for this role at high speeds. We suggest that the neuronal substrate for apparent motion may be distributed over multiple cortical areas, depending upon the speed and spatial interval of the stimulus.

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 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 The contribution of area MT to visual motion perception depends on training

2016 ◽  
Author(s):  
Liu D. Liu ◽  
Christopher C. Pack
Keyword(s):  
Motion Perception ◽  
Visual Motion ◽  
Brain Regions ◽  
Stimulus Motion ◽  
Area Mt ◽  
Temporal Area ◽  
Visual Motion Perception ◽  
Motion Discrimination ◽  
Cortex Area ◽  
Training History

SummaryPerceptual decisions require the transformation of raw sensory inputs into cortical representations suitable for stimulus discrimination. One of the best-known examples of this transformation involves the middle temporal area (MT) of the primate visual cortex. Area MT provides a robust representation of stimulus motion, and previous work has shown that it contributes causally to performance on motion discrimination tasks. Here we report that the strength of this contribution can be highly plastic: Depending on the recent training history, pharmacological inactivation of MT can severely impair motion discrimination, or it can have little detectable influence. Similarly, depending on training, microstimulation can bias motion perception or simply introduce noise. Further analysis of neural and behavioral data suggests that training shifts the readout of motion information between MT and lower-level cortical areas. These results show that the contribution of individual brain regions to conscious perception can shift flexibly depending on sensory experience.

Direction and orientation selectivity of neurons in visual area MT of the macaque

1984 ◽  
Vol 52 (6) ◽  
pp. 1106-1130 ◽  
Author(s):  
T. D. Albright
Keyword(s):  
Direction Selectivity ◽  
Orientation Selectivity ◽  
Orientation Tuning ◽  
Area Mt ◽  
Mt Neurons ◽  
V1 Neurons ◽  
Moving Stimuli ◽  
Preferred Direction ◽  
Visual Area Mt ◽  
Direction Tuning

We recorded from single neurons in the middle temporal visual area (MT) of the macaque monkey and studied their direction and orientation selectivity. We also recorded from single striate cortex (V1) neurons in order to make direct comparisons with our observations in area MT. All animals were immobilized and anesthetized with nitrous oxide. Direction selectivity of 110 MT neurons was studied with three types of moving stimuli: slits, single spots, and random-dot fields. All of the MT neurons were found to be directionally selective using one or more of these stimuli. MT neurons exhibited a broad range of direction-tuning bandwidths to all stimuli (minimum = 32 degrees, maximum = 186 degrees, mean = 95 degrees). On average, responses were strongly unidirectional and of similar magnitude for all three stimulus types. Orientation selectivity of 89 MT neurons was studied with stationary flashed slits. Eighty-three percent were found to be orientation selective. Overall, orientation-tuning bandwidths were significantly narrower (mean = 64 degrees) than direction-tuning bandwidths for moving stimuli. Moreover, responses to stationary-oriented stimuli were generally smaller than those to moving stimuli. Direction selectivity of 55 V1 neurons was studied with moving slits; orientation selectivity of 52 V1 neurons was studied with stationary flashed slits. In V1, compared with MT, direction-tuning bandwidths were narrower (mean = 68 degrees). Moreover, V1 responses to moving stimuli were weaker, and bidirectional tuning was more common. The mean orientation-tuning bandwidth in V1 was also significantly narrower than that in MT (mean = 52 degrees), but the responses to stationary-oriented stimuli were of similar magnitude in the two areas. We examined the relationship between optimal direction and optimal orientation for MT neurons and found that 61% had an orientation preference nearly perpendicular to the preferred direction of motion, as is the case for all V1 neurons. However, another 29% of MT neurons had an orientation preference roughly parallel to the preferred direction. These observations, when considered together with recent reports claiming sensitivity of some MT neurons to moving visual patterns (39), suggest specific neural mechanisms underlying pattern-motion sensitivity in area MT. These results support the notion that area MT represents a further specialization over area V1 for stimulus motion processing. Furthermore, the marked similarities between direction and orientation tuning in area MT in macaque and owl monkey support the suggestion that these areas are homologues.

The response properties of cells in the middle temporal area (area MT) of owl monkey visual cortex

1980 ◽  
Vol 207 (1167) ◽  
pp. 239-248 ◽  
Keyword(s):  
Visual Cortex ◽  
Single Cells ◽  
Area Mt ◽  
Temporal Area ◽  
Middle Temporal ◽  
Owl Monkey ◽  
Monocular Stimulation ◽  
Binocular Stimulation ◽  
Middle Temporal Area ◽  
Monkey Visual Cortex

Recordings from 178 single cells in the middle temporal area (area MT) of owl monkey showed that most cells there are orientation- and direction-selective. They also revealed that a powerful range of binocular inter­actions occur in area MT, with 20% of the cells being responsive to binocular stimulation only, 5% to monocular stimulation only and about 50% of all cells showing some degree of interocular interaction.

Visual activity in areas V3a and V3 during reversible inactivation of area V1 in the macaque monkey

1991 ◽  
Vol 66 (5) ◽  
pp. 1493-1503 ◽  
Author(s):  
P. Girard ◽  
P. A. Salin ◽  
J. Bullier
Keyword(s):  
Visual Stimulation ◽  
Single Cells ◽  
Extrastriate Cortex ◽  
Area 17 ◽  
Visual Responses ◽  
Area Mt ◽  
Reversible Inactivation ◽  
Temporal Area ◽  
Visual Activity ◽  
Residual Vision

1. Behavioral studies in the monkey and clinical studies in humans show that some visuomotor functions are spared in case of a V1 lesion. This residual vision appears to be subserved at least partially by visual activity in extrastriate cortex. Earlier studies have demonstrated that neurons in area V2 lose their visual responses when V1 is reversibly inactivated. On the other hand, Rodman and collaborators have recently shown that neurons in the middle temporal area (area MT) remain visually responsive when V1 is lesioned or inactivated. The purpose of the present study was to determine whether area MT is unique among extrastriate cortical areas in containing visually responsive neurons in the absence of input from area 17. 2. A circular part of the opercular region of area V1 was reversibly inactivated by cooling with a Peltier device. In that condition, 149 sites were recorded in the retinotopically corresponding regions of areas V3 and V3a. 3. About 30% of sites in area V3a still responded to visual stimulation when V1 was inactivated. On the contrary, nearly all sites in area V3 ceased to fire to visual stimulation. Receptive-field properties were assessed with qualitative measures; for most single cells or multiunit sites that responded during V1 inactivation, these properties did not change during cooling. 4. These results suggest that area V3a could take part in spared visuomotor abilities in case of a lesion of V1. Areas V3a and MT are both part of the occipitoparietal pathway, which suggests that the residual vision observed after a lesion of area 17 may depend mostly on this pathway.

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