Cited by 135Memory and Neural MechanismsMemory Processes and InfluencesSpatial Cognition and Navigation

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Dissociable networks involved in spatial and temporal order source retrieval

Ekstrom, Arne D., Copara, Milagros S., Isham, Eve A., Wang, Wei-chun, Yonelinas, Andrew P.·2011·NeuroImage

DOI 10.1016/j.neuroimage.2011.02.033

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Abstract

Space and time are important components of our episodic memories. Without this information, we cannot determine the "where and when" of our recent memories, rendering it difficult to disambiguate individual episodes from each other. The neural underpinnings of spatial and temporal order memory in humans remain unclear, in part because of difficulties in disentangling the contributions of these two types of source information. To address this issue, we conducted an experiment in which participants first navigated a virtual city, experiencing unique routes in a specific temporal order and learning about the spatial layout of the city. Spatial and temporal order information were dissociated in our task such that learning one type of information did not facilitate the other behaviorally. This allowed us to then address the extent to which the two types of information involved functionally distinct or overlapping brain areas. During functional magnetic resonance imaging (fMRI), participants retrieved information about the relative distance of stores within the city (spatial task) and the temporal order of stores from each other (temporal task). Comparable hippocampal activity was observed during these two tasks, but greater prefrontal activity was seen during temporal order retrieval whereas greater parahippocampal activity was seen during spatial retrieval. We suggest that while the brain possesses dissociable networks for maintaining and representing spatial layout and temporal order components of episodic memory, this information may converge into a common representation for source memory in areas such as the hippocampus.

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Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
Episodic memory: from mind to brain
Tulving, E. (2002) · Annual Review of Psychology · doi:10.1146/annurev.psych.53.100901.135114 · Cited by 4,950
Memory and consciousness.
Tulving, E. (1985) · Canadian Psychology / Psychologie canadienne · doi:10.1037/h0080017 · Cited by 4,638
SCRIPTS, PLANS, GOALS, AND UNDERSTANDING
Schank, R. C., & Abelson, R. P. (1988) · Elsevier eBooks · doi:10.1016/b978-1-4832-1446-7.50019-4 · Cited by 4,544
Source monitoring.
Johnson, M. K., Hashtroudi, S., & Lindsay, D. S. (1993) · Psychological Bulletin · doi:10.1037/0033-2909.114.1.3 · Cited by 3,392
Improved assessment of significant activation in functional magnetic resonance imaging (fMRI): use of a cluster-size threshold
Forman, S. D., Cohen, J. D., Fitzgerald, M., Eddy, W. F., Mintun, M. A., & Noll, D. C. (1995) · Magnetic Resonance in Medicine · doi:10.1002/mrm.1910330508 · Cited by 3,202
A cortical representation of the local visual environment
Epstein, R. A., & Kanwisher, N. (1998) · Nature · doi:10.1038/33402 · Cited by 3,083
The organization of learning
Gallistel, C. R. (1990) · Cited by 2,571
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401

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Fried, 1998, The hippocampus and human navigation: technical comment, Science, 282

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Authors: Ekstrom, A. D., Copara, M. S., Isham, E. A., Wang, W.-C., & Yonelinas, A. P.
Affiliations: University of California, Davis (US)
Corresponding author: Ekstrom, Arne D.
ORCID: Ekstrom, Arne D.
Isham, Eve A.
Wang, Wei-chun
Yonelinas, Andrew P.
Venue: NeuroImage
Publisher: Elsevier BV
Published: 2011-06
Volume: 56
Issue: 3
Pages: 1803-1813
ISSN: 1053-8119 (ISSN-L)
DOI: 10.1016/j.neuroimage.2011.02.033
OpenAlex: W2088806161
Cited by: 135
References: 70
Citations by year: 2026: 3 · 2025: 2 · 2024: 5 · 2023: 3 · 2022: 4 · 2021: 8 · 2020: 3 · 2019: 9 · 2018: 10 · 2017: 33 · 2016: 9 · 2015: 19 · 2014: 13 · 2013: 9 · 2012: 5
FWCI: 4.33
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: NeuroImage (publishedVersion)
PubMed (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
Keywords: temporal order memory, episodic memory, source memory, hippocampus, prefrontal cortex, parahippocampal cortex, memory retrieval, spatial configuration
MeSH terms: Adult, Computer Graphics, Computer Simulation, Female, Hippocampus, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Monte Carlo Method, Nerve Net, Photic Stimulation, Psychomotor Performance, Mental Recall, Space Perception, Time Perception, Cluster Analysis, Young Adult

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Dissociable networks involved in spatial and temporal order source retrieval

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