Literature DB >> 6864243

Functional properties of neurons in middle temporal visual area of the macaque monkey. II. Binocular interactions and sensitivity to binocular disparity.

J H Maunsell, D C Van Essen.   

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.

Mesh:

Year:  1983        PMID: 6864243     DOI: 10.1152/jn.1983.49.5.1148

Source DB:  PubMed          Journal:  J Neurophysiol        ISSN: 0022-3077            Impact factor:   2.714


  122 in total

1.  Macaque inferior temporal neurons are selective for disparity-defined three-dimensional shapes.

Authors:  P Janssen; R Vogels; G A Orban
Journal:  Proc Natl Acad Sci U S A       Date:  1999-07-06       Impact factor: 11.205

2.  Perceptually bistable three-dimensional figures evoke high choice probabilities in cortical area MT.

Authors:  J V Dodd; K Krug; B G Cumming; A J Parker
Journal:  J Neurosci       Date:  2001-07-01       Impact factor: 6.167

3.  Colour and luminance interactions in the visual perception of motion.

Authors:  Alexandra Willis; Stephen J Anderson
Journal:  Proc Biol Sci       Date:  2002-05-22       Impact factor: 5.349

4.  Cue combination in the motion correspondence problem.

Authors:  P B Hibbard; M F Bradshaw; R A Eagle
Journal:  Proc Biol Sci       Date:  2000-07-07       Impact factor: 5.349

5.  Contribution of middle temporal area to coarse depth discrimination: comparison of neuronal and psychophysical sensitivity.

Authors:  Takanori Uka; Gregory C DeAngelis
Journal:  J Neurosci       Date:  2003-04-15       Impact factor: 6.167

6.  Phase-disparity coding in extrastriate area 19 of the cat.

Authors:  Daniel Mimeault; Valérie Paquet; Franco Lepore; Jean-Paul Guillemot
Journal:  J Physiol       Date:  2002-12-15       Impact factor: 5.182

7.  Short-latency ocular following in humans is dependent on absolute (rather than relative) binocular disparity.

Authors:  D-S Yang; F A Miles
Journal:  Vision Res       Date:  2003-06       Impact factor: 1.886

8.  EEG activity related to preparation and suppression of eye movements in three-dimensional space.

Authors:  Areti Tzelepi; Antoine Lutz; Zoi Kapoula
Journal:  Exp Brain Res       Date:  2004-01-17       Impact factor: 1.972

9.  Global motion perception in 2-year-old children: a method for psychophysical assessment and relationships with clinical measures of visual function.

Authors:  Tzu-Ying Yu; Robert J Jacobs; Nicola S Anstice; Nabin Paudel; Jane E Harding; Benjamin Thompson
Journal:  Invest Ophthalmol Vis Sci       Date:  2013-12-30       Impact factor: 4.799

10.  Impact of chiasma opticum malformations on the organization of the human ventral visual cortex.

Authors:  Falko R Kaule; Barbara Wolynski; Irene Gottlob; Joerg Stadler; Oliver Speck; Martin Kanowski; Synke Meltendorf; Wolfgang Behrens-Baumann; Michael B Hoffmann
Journal:  Hum Brain Mapp       Date:  2014-04-25       Impact factor: 5.038

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