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Direct observation of the neural computations underlying a single decision

View ORCID ProfileNatalie A Steinemann, View ORCID ProfileGabriel M Stine, View ORCID ProfileEric M Trautmann, View ORCID ProfileAriel Zylberberg, View ORCID ProfileDaniel M Wolpert, View ORCID ProfileMichael N Shadlen
doi: https://doi.org/10.1101/2022.05.02.490321
Natalie A Steinemann
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
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  • ORCID record for Natalie A Steinemann
Gabriel M Stine
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
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Eric M Trautmann
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
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Ariel Zylberberg
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
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Daniel M Wolpert
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
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Michael N Shadlen
1Department of Neuroscience, Columbia University, New York, NY 10027, USA
2Zuckerman Mind Brain Behavior Institute, Columbia University, New York, NY 10027, USA
3Howard Hughes Medical Institute, Columbia University, New York, NY 10027, USA
4Kavli Institute for Brain Science, Columbia University, New York, NY 10027, USA
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  • For correspondence: shadlen@columbia.edu
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Abstract

Neurobiological investigations of perceptual decision-making have furnished the first glimpse of a flexible cognitive process at the level of single neurons1,2. Neurons in the parietal and prefrontal cortex3–6 are thought to represent the accumulation of noisy evidence, acquired over time, leading to a decision. Neural recordings averaged over many decisions have provided support for the deterministic rise in activity to a termination bound7. Critically, it is the unobserved stochastic component that is thought to confer variability in both choice and decision time8. Here, we elucidate this stochastic, diffusion-like signal on individual decisions by recording simultaneously from hundreds of neurons in the lateral intraparietal cortex (LIP). We show that a small subset of these neurons, previously studied singly, represent a combination of deterministic drift and stochastic diffusion—the integral of noisy evidence—during perceptual decision making, and we provide direct support for the hypothesis that this diffusion signal is the quantity responsible for the variability in choice and reaction times. Neuronal state space and decoding analyses, applied to the whole population, also identify the drift diffusion signal. However, we show that the signal relies on the subset of neurons with response fields that overlap the choice targets. This parsimonious observation would escape detection by these powerful methods, absent a clear hypothesis.

Competing Interest Statement

The authors have declared no competing interest.

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The copyright holder for this preprint is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made available under a CC-BY 4.0 International license.
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Posted May 04, 2022.
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Direct observation of the neural computations underlying a single decision
Natalie A Steinemann, Gabriel M Stine, Eric M Trautmann, Ariel Zylberberg, Daniel M Wolpert, Michael N Shadlen
bioRxiv 2022.05.02.490321; doi: https://doi.org/10.1101/2022.05.02.490321
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Direct observation of the neural computations underlying a single decision
Natalie A Steinemann, Gabriel M Stine, Eric M Trautmann, Ariel Zylberberg, Daniel M Wolpert, Michael N Shadlen
bioRxiv 2022.05.02.490321; doi: https://doi.org/10.1101/2022.05.02.490321

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