Evidence map›Paper›PMID 41996451›Full record

ArticlePLoS biology2026

Neural population dynamics and temporal context cells in macaque medial parietal cortex support temporal order memory.

Shuzhen Zuo, Chenyu Wang, Lei Wang, Zhiyong Jin, Xufeng Zhou, Ning Su, Jianhua Liu, Thomas J McHugh, Makoto Kusunoki, Sze Chai Kwok

Abstract read
In one paragraph

Article in PLoS biology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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.

2 · The registry

The trial behind it

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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Article
  2. Sustained Hippocampal Theta Oscillations Reflect Experience-Dependent Learning in Backward Temporal Order Memory Retrieval.The Journal of neuroscience : the official journal of the Society for Neuroscience · 2025
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Shuzhen ZuoShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Chenyu WangPhylo-Cognition Laboratory, Duke Kunshan University - The First People's Hospital of Kunshan Joint Brain Sciences Laboratory, Division of Natural and Applied Sciences, Digital Innovation Research Center, Duke Institute for Brain Sciences, Duke Kunshan University, Kunshan, Jiangsu, China.
Lei WangShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Zhiyong JinShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Xufeng ZhouShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Ning SuShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Jianhua LiuShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.
Thomas J McHughDepartment of Life Sciences, Graduate School of Arts and Sciences, The University of Tokyo, Tokyo, Japan.
Makoto KusunokiMRC Cognition and Brain Sciences Unit, University of Cambridge, United Kingdom.
Sze Chai KwokShanghai Key Laboratory of Brain Functional Genomics, Key Laboratory of Brain Functional Genomics (Ministry of Education), School of Psychology and Cognitive Science, East China Normal University, Shanghai, China.ORCID https://orcid.org/0000-0002-7439-1193

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Episodic memory involves encoding and remembering the order of events experienced over time. Previous work examining the mechanisms of temporal order memories has focused primarily on the hippocampus and prefrontal cortices, with comparatively less attention paid to population-level memory signals in the medial posterior parietal cortex (mPPC). Combining in vivo multi-unit electrophysiology and a temporal order judgment task with naturalistic cinematic material in macaques, we show that population activity in mPPC exhibits temporally structured dynamics during both encoding and retrieval. During encoding, mPPC neuronal ensembles exhibit gradually evolving activity patterns consistent with temporal context representations embedded in the unfolding video episodes, whereas during retrieval these neurons engage in coordinated, synchronous activity preceding memory-guided decisions. Moreover, trial-by-trial similarity between population activity patterns during encoding and retrieval predicts temporal order judgment performance. A separate control experiment further ruled out eye saccades, fixation patterns, and scan paths as confounding factors contributing to the observed neural dynamics. Together, these findings suggest that mPPC contributes to temporal order memory through population-level representations that integrate temporally extended experience with retrieval-related decision processes, rather than through simple sensory-driven or motor-related responses.

Indexed as

MemoryMemory, EpisodicNeuronsParietal LobeAnimalsMacaca mulattaMaleSaccades

Identifiers

PMID41996451
PMCPMC13108878

What OpenQuestion holds

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LicenceCC BY
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Registered trials

None linked

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.