ReviewCognition2020
Reward prediction errors create event boundaries in memory.
Review in Cognition, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 58 papers.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
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Who cites it
58 citing papers in PubMed.
- Effects of Initial Experiences on Risky Choice.Quarterly journal of experimental psychology (2006) · 2026Article
- A dynamic affective surprise signal influences episodic memory.Cognition · 2026Article
- The role of context in continuity and segmentation.Nature human behaviour · 2026Article
- Confidence in naturalistic decision making.Neuroscience of consciousness · 2026Article
- Prediction error is out of context: The dominance of contextual stability in structuring episodic memories.Psychonomic bulletin & review · 2025Article
- Neural Representation of Episodic Time.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025Review
- Sequence-to-sequence models with attention mechanistically map to the architecture of human memory search.Communications psychology · 2025Article
- Aberrant neural event segmentation during a continuous social narrative in trauma-exposed older adolescents and young adults.Cognitive, affective & behavioral neuroscience · 2025Article
- Locus coeruleus activation 'resets' hippocampal event representations and separates adjacent memories.bioRxiv : the preprint server for biology · 2025Article
- Prediction of information value influences memory: the effect of predicted and assigned value on memory.Memory (Hove, England) · 2025Article
- Using computational models of learning to advance cognitive behavioral therapy.Communications psychology · 2025Review
- Free recall is shaped by inference and scaffolded by event structure.Communications psychology · 2025Article
- Schemas, reinforcement learning and the medial prefrontal cortex.Nature reviews. Neuroscience · 2025Review
- A Retrieved Context Model of Serial Recall and Free Recall.Computational brain & behavior · 2025Article
- The influence of emotion on temporal context models.Cognition & emotion · 2025Review
- Article
- Event Segmentation Promotes the Reorganization of Emotional Memory.Journal of cognitive neuroscience · 2025Article
- The Relationship between Event Boundary Strength and Pattern Shifts across the Cortical Hierarchy during Naturalistic Movie-viewing.Journal of cognitive neuroscience · 2024Article
- The Ubiquity of Time in Latent-cause Inference.Journal of cognitive neuroscience · 2024Article
- Time after Time: Preserving Temporal Memories When Experiences Repeat.Journal of cognitive neuroscience · 2024Review
Corrections and comments
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Authors and funding
4 authors.
Funding
Abstract
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.
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Registered trials
Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.