Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity
- 1 May 1983
- journal article
- research article
- Published by American Physiological Society in Journal of Neurophysiology
- Vol. 49 (5), 1148-1167
- https://doi.org/10.1152/jn.1983.49.5.1148
Abstract
1. Electrophysiological recordings were made in the middle temporal visual area (MT) of five macaque monkeys. Binocularity and selectivity for disparity were examined using a computer-driven stimulator to activate each eye independently. Results were obtained from 91 single units in MT. 2. Most units in MT receive approximately balanced inputs from the two eyes, and very few could be driven through only one eye. 3. In one type of test for disparity selectivity, units were examined with stimuli that had different but fixed horizontal disparities, thereby simulating frontoparallel movements at different distances from the animal. About two-thirds of ;the units tested for fixed disparity selectivity (52/76) showed pronounced sensitivity to horizontal disparity. Most of these units could be grouped into the same four classes of disparity-tuned units that have previously been described in V1 and V2 of the macaque: near, far, tuned excitatory, and tuned inhibitory. 4. Twenty units were tested for sensitivity to vertical stimulus disparity, which does not normally contribute to stereopsis. Most were as sensitive to vertical disparities as to horizontal. 5. Units were also tested for selectivity for stimuli that moved with changing disparity, simulating trajectories with components of motion toward or away from the animal (motion in depth). No units were found to be truly selective for motion in depth. Units tuned for fixed disparity could appear to prefer motion in depth if tested only with trajectories whose common center point was far from the unit's optimal fixed disparity. However, we do not consider this to represent genuine selectivity for motion in depth, since 1) the responses ara adequately and more easily explained in terms of selectivity for fixed disparity and 2) the best overall response of these units is to frontoparallel motion at the optimal fixed disparity. This observation bears importantly on the interpretation of motion in depth selectivity in previous investigations. 6. The presence of a substantial degree of selectivity for fixed disparity in MT, together with previously demonstrated selectivities for direction and speed, indicates that MT is well suited for the analysis of motion in three-dimensional space.This publication has 15 references indexed in Scilit:
- Uniformity and diversity of structure and function in rhesus monkey prestriate visual cortex.The Journal of Physiology, 1978
- Neurones in cat parastriate cortex sensitive to the direction of motion in three‐dimensional spaceThe Journal of Physiology, 1978
- Binocular interaction and depth sensitivity in striate and prestriate cortex of behaving rhesus monkeyJournal of Neurophysiology, 1977
- Discrimination of orientation and position disparities by binocularly activated neurons in cat straite cortexJournal of Neurophysiology, 1977
- Binocular visual mechanisms in cortical areas I and II of the sheep.The Journal of Physiology, 1976
- The origin of efferent pathways from the primary visual cortex, area 17, of the macaque monkey as shown by retrograde transport of horseradish peroxidaseJournal of Comparative Neurology, 1975
- Receptive fields and functional architecture of monkey striate cortexThe Journal of Physiology, 1968
- The neural mechanism of binocular depth discriminationThe Journal of Physiology, 1967
- Retinal disparity and diplopiaVision Research, 1966
- XVIII. Contributions to the physiology of vision. —Part the first. On some remarkable, and hitherto unobserved, phenomena of binocular visionPhilosophical Transactions of the Royal Society of London, 1838