Publications by Year: 2020

2020
Drummond, N., & Niv, Y. (2020). Model-based decision making and model-free learning. Current Biology , 30 (15), 860-865. Publisher's VersionAbstract
Free will is anything but free. With it comes the onus of choice: not only what to do, but which inner voice to listen to — our ‘automatic’ response system, which some consider ‘impulsive’ or ‘irrational’, or our supposedly more rational deliberative one. Rather than a devil and angel sitting on our shoulders, research suggests that we have two decision-making systems residing in the brain, in our basal ganglia. Neither system is the devil and neither is irrational. They both have our best interests at heart and aim to suggest the best course of action calculated through rational algorithms. However, the algorithms they use are qualitatively different and do not always agree on which action is optimal. The rivalry between habitual, fast action and deliberative, purposeful action is an ongoing one.
Rouhani, N., Norman, K. A., Niv, Y., & Bornstein, A. M. (2020). Reward prediction errors create event boundaries in memory. Cognition. PDFAbstract
We remember when things change. Particularly salient are experiences where there is a change in rewards, eliciting reward prediction errors (RPEs). How do RPEs influence our memory of those experiences? One idea is that this signal directly enhances the encoding of memory. Another, not mutually exclusive, idea is that the RPE signals a deeper change in the environment, leading to the mnemonic separation of subsequent experiences from what came before, thereby creating a new latent context and a more separate memory trace. We tested this in four experiments where participants learned to predict rewards associated with a series of trial-unique images. High-magnitude RPEs indicated a change in the underlying distribution of rewards. To test whether these large RPEs created a new latent context, we first assessed recognition priming for sequential pairs that included a high-RPE event or not (Exp. 1: n = 27 & Exp. 2: n = 83). We found evidence of recognition priming for the high-RPE event, indicating that the high-RPE event is bound to its predecessor in memory. Given that high-RPE events are themselves preferentially remembered (Rouhani, Norman, & Niv, 2018), we next tested whether there was an event boundary across a high-RPE event (i.e., excluding the high-RPE event itself; Exp. 3: n = 85). Here, sequential pairs across a high RPE no longer showed recognition priming whereas pairs within the same latent reward state did, providing initial evidence for an RPE-modulated event boundary. We then investigated whether RPE event boundaries disrupt temporal memory by asking participants to order and estimate the distance between two events that had either included a high-RPE event between them or not (Exp. 4). We found (n = 49) and replicated (n = 77) worse sequence memory for events across a high RPE. In line with our recognition priming results, we did not find sequence memory to be impaired between the high-RPE event and its predecessor, but instead found worse sequence memory for pairs across a high-RPE event. Moreover, greater distance between events at encoding led to better sequence memory for events across a low-RPE event, but not a high-RPE event, suggesting separate mechanisms for the temporal ordering of events within versus across a latent reward context. Altogether, these findings demonstrate that high-RPE events are both more strongly encoded, show intact links with their predecessor, and act as event boundaries that interrupt the sequential integration of events. We captured these effects in a variant of the Context Maintenance and Retrieval model (CMR; Polyn, Norman, & Kahana, 2009), modified to incorporate RPEs into the encoding process.
Cai, M. B., Shvartsman, M., Wu, A., Zhang, H., & Ju, X. (2020). Incorporating structured assumptions with probabilistic graphical models in fMRI data analysis. Neuropsychologia. Publisher's VersionAbstract
With the wide adoption of functional magnetic resonance imaging (fMRI) by cognitive neuroscience researchers, large volumes of brain imaging data have been accumulated in recent years. Aggregating these data to derive scientific insights often faces the challenge that fMRI data are high-dimensional, heterogeneous across people, and noisy. These challenges demand the development of computational tools that are tailored both for the neuroscience questions and for the properties of the data. We review a few recently developed algorithms in various domains of fMRI research: fMRI in naturalistic tasks, analyzing full-brain functional connectivity, pattern classification, inferring representational similarity and modeling structured residuals. These algorithms all tackle the challenges in fMRI similarly: they start by making clear statements of assumptions about neural data and existing domain knowledge, incorporate those assumptions and domain knowledge into probabilistic graphical models, and use those models to estimate properties of interest or latent structures in the data. Such approaches can avoid erroneous findings, reduce the impact of noise, better utilize known properties of the data, and better aggregate data across groups of subjects. With these successful cases, we advocate wider adoption of explicit model construction in cognitive neuroscience. Although we focus on fMRI, the principle illustrated here is generally applicable to brain data of other modalities.
Langdon, A. J., & Daw, N. (2020). Beyond the Average View of Dopamine. Trends in Cognitive Sciences. PDFAbstract
Dopamine (DA) responses are synonymous with the ‘reward prediction error’ of reinforcement learning (RL), and are thought to update neural estimates of expected value. A recent study by Dabney et al. enriches this picture, demonstrating that DA neurons track variability in rewards, providing a readout of risk in the brain.
Sharpe, M. J., Batchelor, H. M., Mueller, L. E., Chang, C. Y., Maes, E. J. P., Niv, Y., & Schoenbaum, G. (2020). Dopamine transients do not act as model-free prediction errors during associative learning. Nature Communications , 11 (1), 106. Publisher's Version