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Richard T Born

Publications and source records attributed to Richard T Born.

10 recordsLinked to original sources
PubMed2006

Spatiotemporal structure of nonlinear subunits in macaque visual cortex.

The primate visual system is arranged hierarchically, starting from the retina and continuing through a series of extrastriate visual areas. Selectivity for motion is first found in individual neurons in the primate visual cortex (V1), in which many simple cells respond selectively to the direction and speed of moving stimuli. Beyond simple cells, most studies of direction selectivity have focused on either V1 complex cells or neurons in the middle temporal area (MT/V5). To understand how visual information is transferred along this pathway, we have studied all three types of neurons, using a reverse correlation procedure to obtain high spatial and temporal resolution maps of activity for different motion stimuli. Most complex and MT cells showed strong second-order interactions, indicating that they were tuned for particular displacements of an apparent motion stimulus. The spatiotemporal structure of these interactions showed a high degree of similarity between the populations of V1 complex cells and MT cells, in terms of the spatiotemporal limits and preferences for motion and their two-dimensional spatial structure. Much of the structure in the V1 and MT second-order kernels could be accounted for on the basis of the first-order responses of V1 simple cells, under the assumption of a Reichardt or motion-energy type of computation.

Animals↗
PubMed2006

Temporal evolution of 2-dimensional direction signals used to guide eye movements.

The smooth pursuit system must integrate many local motion measurements into a coherent estimate of target velocity. Several laboratories have studied this integration process using eye movements elicited by targets, such as tilted bars, containing conflicts between local motion signals measured along contours [one dimensional (1D)] and those measured at the bar's endpoints, or terminators [two dimensional (2D)]. The general finding is that 1D signals dominate early responses, whereas later components of the behavior are determined by 2D signals. We studied the dynamics of the integration process in macaque monkeys by systematically varying the relative proportions of 1D and 2D signals and the retinal eccentricities at which they appeared. Predictably, longer bars produced greater and longer-lasting contour-induced deviations. The evolution of the 2D response occurred over a period of 50-400 ms, depending on the relative proportions of 1D and 2D signals. As contours were displaced from the fovea the deviation decreased but much less so for early (1st 40 ms) than for late (subsequent 40 ms) pursuit initiation. These bottom-up effects could be overcome to a limited extent by the top-down influence of predictability. Finally, we observed that when animals were free to track any part of the bar, they spontaneously made short-latency saccades to the terminators on most trials, especially when the bars were tilted. This suggests an increased saliency of moving terminators, particularly when discrepancies exist among local motion signals.

Adaptation, Ocular↗
PubMed2005

Structure and function of visual area MT.

The small visual area known as MT or V5 has played a major role in our understanding of the primate cerebral cortex. This area has been historically important in the concept of cortical processing streams and the idea that different visual areas constitute highly specialized representations of visual information. MT has also proven to be a fertile culture dish--full of direction- and disparity-selective neurons--exploited by many labs to study the neural circuits underlying computations of motion and depth and to examine the relationship between neural activity and perception. Here we attempt a synthetic overview of the rich literature on MT with the goal of answering the question, What does MT do?

Animals↗
PubMed2004

Contrast dependence of suppressive influences in cortical area MT of alert macaque.

Visual neurons are often characterized in terms of their tuning for various stimulus properties, such as shape, color, and velocity. Generally, these tuning curves are further modulated by the overall intensity of the stimulus, such that increasing the contrast increases the firing rate, up to some maximum. In this paper, we describe the tuning of neurons in the middle temporal area (MT or V5) of macaque visual cortex for moving stimuli of varying contrast. We find that, for some MT neurons, tuning curves for stimulus direction, speed, and size are shaped in part by suppressive influences that are present at high stimulus contrast but weak or nonexistent at low contrast. For most neurons, the suppression is direction-specific and strongest for large, slow-moving stimuli. The surprising consequence of this phenomenon is that some MT neurons actually fire more vigorously to a large low-contrast stimulus than to one of high contrast. These results are consistent with recent perceptual observations, as well as with information-theoretic models, which hypothesize that the visual system seeks to reduce redundancy at high contrast while maintaining sensitivity at low contrast.

Action Potentials↗
PubMed2004

Taking strategies to task.

In this issue of Neuron, Uka and DeAngelis report a neural signature of the strategy that monkeys' brains developed to solve a visual discrimination task by training them on one version of the task and testing them on another. Extensive training on one version caused decision networks in the animals' brains to ignore certain classes of neurons whose signals would have been useful on the modified version of the task used to test them.

Animals↗
PubMed2004

Integration of Contour and Terminator Signals in Visual Area MT of Alert Macaque.

The integration of visual information is a critical task that is performed by neurons in the extrastriate cortex of the primate brain. For motion signals, integration is complicated by the geometry of the visual world, which renders some velocity measurements ambiguous and others incorrect. The ambiguity arises because neurons in the early stages of visual processing have small receptive fields, which can only recover the component of motion perpendicular to the orientation of a contour (the aperture problem). Unambiguous motion signals are located at end points and corners, which are referred to as terminators. However, when an object moves behind an occluding surface, motion measurements made at the terminators formed by the intersection of the object and the occluder are generally not consistent with the direction of object motion. To study how cortical neurons integrate these different motion cues, we used variations on the classic "barber pole" stimulus and measured the responses of neurons in the middle temporal area (MT or V5) of extrastriate cortex of alert macaque monkeys. Our results show that MT neurons are more strongly influenced by the unambiguous motion signals generated by terminators than to the ambiguous signals generated by contours. Furthermore, these neurons respond better to terminators that are intrinsic to a moving object than to those that are accidents of occlusion. V1 neurons show similar response patterns to local cues (contours and terminators), but for large stimuli, they do not reflect the global motion direction computed by MT neurons. These observations are consistent with psychophysical findings that show that our perception of moving objects often depends on the motion of terminators.

Animals↗
PubMed2003

End-stopping and the aperture problem: two-dimensional motion signals in macaque V1.

Our perception of fine visual detail relies on small receptive fields at early stages of visual processing. However, small receptive fields tend to confound the orientation and velocity of moving edges, leading to ambiguous or inaccurate motion measurements (the aperture problem). Thus, it is often assumed that neurons in primary visual cortex (V1) carry only ambiguous motion information. Here we show that a subpopulation of V1 neurons is capable of signaling motion direction in a manner that is independent of contour orientation. Specifically, end-stopped V1 neurons obtain accurate motion measurements by responding only to the endpoints of long contours, a strategy which renders them largely immune to the aperture problem. Furthermore, the time course of end-stopping is similar to the time course of motion integration by MT neurons. These results suggest that cortical neurons might represent object motion by responding selectively to two-dimensional discontinuities in the visual scene.

Animals↗
PubMed2003

Two-dimensional substructure of stereo and motion interactions in macaque visual cortex.

The analysis of object motion and stereoscopic depth are important tasks that are begun at early stages of the primate visual system. Using sparse white noise, we mapped the receptive field substructure of motion and disparity interactions in neurons in V1 and MT of alert monkeys. Interactions in both regions revealed subunits similar in structure to V1 simple cells. For both motion and stereo, the scale and shape of the receptive field substructure could be predicted from conventional tuning for bars or dot-field stimuli, indicating that the small-scale interactions were repeated across the receptive fields. We also found neurons in V1 and in MT that were tuned to combinations of spatial and temporal binocular disparities, suggesting a possible neural substrate for the perceptual Pulfrich phenomenon. Our observations constrain computational and developmental models of motion-stereo integration.

Animals↗
PubMed2002

Integration of motion cues for the initiation of smooth pursuit eye movements.

To clearly see a moving object, an observer must rotate his or her eyes with a velocity that matches that of the object. Such rotations are called smooth pursuit eye movements, and they depend critically on the ability of the primate brain to integrate information about object velocity from various local motion signals. When the local motion signals are in conflict, it is possible to use smooth pursuit eye movements as a continuous read-out of the motion integration process. This review discusses the results of recent behavioral experiments that have taken this approach, along with relevant neurophysiological and computational studies.

Animals↗