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Wyart, V.

Publications and source records attributed to Wyart, V..

2 recordsLinked to original sources

Computational noise in reward-guided learning drives behavioral variability in volatile environments

When learning the value of actions in volatile environments, humans often make seemingly irrational decisions which fail to maximize expected value. We reasoned that these non-greedy decisions, instead of reflecting information seeking during choice, may be caused by computational noise in the learning of action values. Here, using reinforcement learning (RL) models of behavior and multimodal neurophysiological data, we show that the majority of non-greedy decisions stems from this learning noise. The trial-to-trial variability of sequential learning steps and their impact on behavior could be predicted both by BOLD responses to obtained rewards in the dorsal anterior cingulate cortex (dACC) and by phasic pupillary dilation - suggestive of neuromodulatory fluctuations driven by the locus coeruleus-norepinephrine (LC-NE) system. Together, these findings indicate that most of behavioral variability, rather than reflecting human exploration, is due to the limited computational precision of reward-guided learning.

neuroscience

Tracking the Canonical Computations of Perceptual Processing in a Quasi-Continuous Sensory Flow

The canonical computations involved in sensory processing, such as neural adaptation and prediction-error signals, have mainly derived from studies investigating the neural responses elicited by a single stimulus. Here, we test whether these computations can be tracked in a quasi-continuous flow of visual stimulation, by correlating scalp electroencephalography (EEG) recordings to simulations of neuronal populations. Fifteen subjects were presented with ~5,000 visual gratings presented in rapid sequences. Our results show that we can simultaneously decode, from the EEG sensors, up to 4 visual stimuli presented sequentially. Temporal generalization and source analyses reveal that the information contained in each stimulus is processed by a \"visual pipeline\": a long cascade of transient processing stages, which can overall encode multiple stimuli at once. Importantly, our data suggest that the early feedforward activity but not the late feedback responses are marked by an adaptation phenomenon. Overall, our approach demonstrates how theoretically-derived computations, as isolated in single-stimulus paradigms, can be generalized to conditions of a continuous flow of sensory information.

neuroscience