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Journal of Neuroscience, Vol 16, 1486-1510, Copyright © 1996 by Society for Neuroscience
A computational analysis of the relationship between neuronal and behavioral responses to visual motion
MN Shadlen, KH Britten, WT Newsome and JA Movshon
Department of Neurobiology, Stanford University School of Medicine, California 94305, USA.
We have documented previously a close relationship between neuronal
activity in the middle temporal visual area (MT or V5) and behavioral
judgments of motion (Newsome et al., 1989; Salzman et al., 1990; Britten et
al., 1992; Britten et al., 1996). We have now used numerical simulations to
try to understand how neural signals in area MT support psychophysical
decisions. We developed a model that pools neuronal responses drawn from
our physiological data set and compares average responses in different
pools to produce psychophysical decisions. The structure of the model
allows us to assess the relationship between "neuronal" input signals and
simulated psychophysical performance using the same methods we have applied
to real experimental data. We sought to reconcile three experimental
observations: psychophysical performance (threshold sensitivity to motion
stimuli embedded in noise), a trial-by-trial covariation between the neural
response and the monkey's choices, and a modest correlation between pairs
of MT neurons in their variable responses to identical visual stimuli. Our
results can be most accurately simulated if psychophysical decisions are
based on pools of at least 100 weakly correlated sensory neurons. The
neurons composing the pools must include a broader range of sensitivities
than we encountered in our MT recordings, presumably because of the
inclusion of neurons whose optimal stimulus is different from the one being
discriminated. Central sources of noise degrade the signal-to-noise ratio
of the pooled signal, but this degradation is relatively small compared
with the noise typically carried by single cortical neurons. This suggests
that our monkeys base near-threshold psychophysical judgments on signals
carried by populations of weakly interacting neurons; these populations
include many neurons that are not tuned optimally for the particular
stimuli being discriminated.
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S. J. D. Prince, A. D. Pointon, B. G. Cumming, and A. J. Parker
The Precision of Single Neuron Responses in Cortical Area V1 during Stereoscopic Depth Judgments
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S. Furukawa, L. Xu, and J. C. Middlebrooks
Coding of Sound-Source Location by Ensembles of Cortical Neurons
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A. W. Goodwin and H. E. Wheat
Effects of Nonuniform Fiber Sensitivity, Innervation Geometry, and Noise on Information Relayed by a Population of Slowly Adapting Type I Primary Afferents from the Fingerpad
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L. J. Croner and T. D. Albright
Segmentation by Color Influences Responses of Motion-Sensitive Neurons in the Cortical Middle Temporal Visual Area
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R. Azouz and C. M. Gray
Cellular Mechanisms Contributing to Response Variability of Cortical Neurons In Vivo
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K. H. Britten and W. T. Newsome
Tuning Bandwidths for Near-Threshold Stimuli in Area MT
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M. N. Shadlen and W. T. Newsome
The Variable Discharge of Cortical Neurons: Implications for Connectivity, Computation, and Information Coding
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D. Lee, N. L. Port, W. Kruse, and A. P. Georgopoulos
Variability and Correlated Noise in the Discharge of Neurons in Motor and Parietal Areas of the Primate Cortex
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E. Salinas and R. Romo
Conversion of Sensory Signals into Motor Commands in Primary Motor Cortex
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S. C. de Oliveira, A. Thiele, and K.-P. Hoffmann
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V. P. Ferrera and S. G. Lisberger
Neuronal Responses in Visual Areas MT and MST During Smooth Pursuit Target Selection
J Neurophysiol,
September 1, 1997;
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M. Gur, A. Beylin, and D. M. Snodderly
Response Variability of Neurons in Primary Visual Cortex (V1) of Alert Monkeys
J. Neurosci.,
April 15, 1997;
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A. Arieli, A. Sterkin, A. Grinvald, and A. Aertsen
Dynamics of Ongoing Activity: Explanation of the Large Variability in Evoked Cortical Responses
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