Cited by 191Memory Processes and InfluencesMemory and Neural MechanismsCognitive Functions and Memory

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Medial Temporal Lobe Activity during Source Retrieval Reflects Information Type, not Memory Strength

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Diana, Rachel A., Yonelinas, Andrew P., Ranganath, Charan·2010·Journal of Cognitive Neuroscience

DOI 10.1162/jocn.2009.21335PMC PMC2862119

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Abstract

The medial temporal lobes (MTLs) are critical for episodic memory but the functions of MTL subregions are controversial. According to memory strength theory, MTL subregions collectively support declarative memory in a graded manner. In contrast, other theories assert that MTL subregions support functionally distinct processes. For instance, one view is that perirhinal cortex (PRc) processes item information, parahippocampal cortex (PHc) processes context information, and the hippocampus binds item and context. Here, we report two experiments that tested competing predictions from these models. In these studies, subjects encoded color-word associations by imagining color either as a contextual association (context detail condition) or as a feature of the item to be encoded (item detail condition). Results showed that encoding color information as an item detail improved source recognition in amnesic patients with recollection deficits. Furthermore, event-related fMRI data from healthy subjects revealed PRc activation associated with successful retrieval of item details, whereas activation in the hippocampus and PHc was associated with recollection-based source retrieval. The qualitatively different patterns of results observed in PRc and hippocampus/PHc are inconsistent with a memory strength account and are consistent with the idea that different MTL regions process different types of episodic information.

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Detection Theory: A User's Guide
Macmillan, N. A., & Creelman, C. D. (1991) · Cited by 5,415
The Nature of Recollection and Familiarity: A Review of 30 Years of Research
Yonelinas, A. P. (2002) · Journal of Memory and Language · doi:10.1006/jmla.2002.2864 · Cited by 3,840
Detection theory: A user's guide
Lories, G. (1993) · Behavioural Processes · doi:10.1016/0376-6357(93)90083-4 · Cited by 2,903
The Medial Temporal Lobe and Recognition Memory
Eichenbaum, H., Yonelinas, A. P., & Ranganath, C. (2007) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.30.051606.094328 · Cited by 2,580
Self-citation
Recognition memory: What are the roles of the perirhinal cortex and hippocampus?
Brown, M. W., & Aggleton, J. P. (2001) · Nature reviews. Neuroscience · doi:10.1038/35049064 · Cited by 1,624
Memory, amnesia, and the hippocampal system
(1994) · Choice Reviews Online · doi:10.5860/choice.31-5148 · Cited by 1,533
The hippocampus and memory: insights from spatial processing
Bird, C. M., & Burgess, N. (2008) · Nature Reviews Neuroscience · doi:10.1038/nrn2335 · Cited by 1,313
The Variability of Human, BOLD Hemodynamic Responses
Aguirre, G. K., Zarahn, E., & D’Esposito, M. (1998) · NeuroImage · doi:10.1006/nimg.1998.0369 · Cited by 1,251
Imaging recollection and familiarity in the medial temporal lobe: a three-component model
Diana, R. A., Yonelinas, A. P., & Ranganath, C. (2007) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2007.08.001 · Cited by 1,231
Receiver-operating characteristics in recognition memory: Evidence for a dual-process model.
Yonelinas, A. P. (1994) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037//0278-7393.20.6.1341 · Cited by 1,152

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Wang, W., Dew, I. T. Z., & Cabeza, R. E. L. (2014) · Brain Research · doi:10.1016/j.brainres.2014.09.061 · Cited by 21
Sex and age differentially affect GABAergic neurons in the mouse prefrontal cortex and hippocampus following chronic intermittent hypoxia
Rubin, B. R., Milner, T. A., Pickel, V. M., Coleman, C. G., Marques-Lopes, J., Kempen, T. A. V., Kazim, S. F., McEwen, B. S., Gray, J. D., & Pereira, A. C. (2019) · Experimental Neurology · doi:10.1016/j.expneurol.2019.113075 · Cited by 19
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Duarte, A., & Dulas, M. R. (2020) · Cambridge University Press eBooks · doi:10.1017/9781108552684.013 · Cited by 22
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Ludmer, R., Edelson, M. G., & Dudai, Y. (2014) · Hippocampus · doi:10.1002/hipo.22369 · Cited by 4
Chinese character unitization enhances item memory in addition to associative memory: Evidence from ERP and TFR.
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Dulas, M. R., Schwarb, H. D., Cannavale, C. N., & Cohen, N. J. (2021) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/bs.plm.2021.07.001 · Cited by 3
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Stevenson, C. H. (2011) · ERA · Cited by 4
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Yudhasmara, A., Adani, A. K., Dewi, I. N., Judarwanto, W., & Yudhasmara, S. (2024) · Journal of Social Science (JoSS) · doi:10.57185/joss.v3i2.285 · Cited by 2
Age-related decline in source and associative memory
Sümer, E., & Kaynak, H. (2024) · Cognitive Processing · doi:10.1007/s10339-024-01230-z · Cited by 3
La mémoire déclarative et le modèle de Squire
Jaffard, R. (2011) · Revue de neuropsychologie · doi:10.3917/rne.032.0083 · Cited by 2
The missing link? Testing a schema account of unitizationPreprint
Tibon, R., Greve, A., & Henson, R. N. (2017) · doi:10.31234/osf.io/49pfs · Cited by 2
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Soch, J., Richter, A., Schott, B. H., & Kizilirmak, J. M. (2022) · doi:10.31234/osf.io/u5t82 · Cited by 2
Improving memory through choice and deliberation in decision‐making: Evidence from ERPs
Zhang, J., Dai, J., Tian, L., Xu, Z., Zhang, M., Zhang, P., Guo, C., & Li, Q. (2024) · Psychophysiology · doi:10.1111/psyp.14662 · Cited by 1
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Zhang, Z., Zhou, Y., Zeng, Y., & Xing, Q. (2025) · Psychological Research · doi:10.1007/s00426-025-02182-5 · Cited by 1
Developmental differences in relations between parent-reported executive function and unitized and non-unitized memory representations during childhood
Blankenship, S. L., & Riggins, T. (2015) · Frontiers in Psychology · doi:10.3389/fpsyg.2015.01214 · Cited by 1
Investigating the item recognition in associative memory: A unitization perspective
Zejun, L. I. U., Wang, Y., & Guo, C. (2019) · Advances in Psychological Science · doi:10.3724/sp.j.1042.2019.00490 · Cited by 1
Recognition memory: familiarity signals increase selectively in the lateral entorhinal cortex following hippocampal lesionsPreprint
Mahnke, L., Atucha, E., Kitsukawa, T., & Sauvage, M. M. (2020) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2020.06.16.131763 · Cited by 1
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Hou, M., Hill, P. F., Aktas, A. N. Z., Ekstrom, A. D., & Rugg, M. D. (2024) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2024.06.10.598309 · Cited by 1
Remembering and knowing : exploring subjective report, familiarity, and confidence
Williams, H. L. (2011) · UPT. Syiah Kuala University Library (Syiah Kuala University)
The role of the medial temporal lobe in discriminating complex object and scene stimuli
Shine, J. P. (2013) · ORCA Online Research @Cardiff (Cardiff University)
RECOLLECTION OF EPISODIC MEMORY AND THE HIPPOCAMPUS: EVIDENCE FROM FMRI
Suzuki, M. (2012) · PSYCHOLOGIA · doi:10.2117/psysoc.2012.63
Investigating Familiarity's Contribution to Source Recognition
Mollison, M. V., Mollison, W. M. V., Curran, T., Kim, A., & Miyake, A. (2010) · ProQuest Demo Repository
The Fuld Object Memory Evaluation: A Study of Validity, Clinical Utility, and the Effects of Extending the Delay
Aguilar, C. (2014)
INFLUENCE OF EXECUTIVE FUNCTIONING ON MEMORY FOR CONTEXTUAL DETAILS AND FALSE RECOGNITION
Rollins, L. (2012) · University Libraries (University of Maryland)
DoubleDissociationbetweenHippocampaland ParahippocampalResponsestoObject-Background ContextandSceneNovelty
Howard, L. R., & Ólafsdóttir, H. F. (2011)
ARoleforPerirhinalCortexinMemoryforNovel Object-ContextAssociations
Watson, H. C. (2012)
Separating Patterns of Space and Time: Differences in Memory for Event Duration and Sequential Order
Brunec, I. K. (2015) · TSpace (University of Toronto)
Dynamic integration of conceptual information during learningPreprint
Inhoff, M. C., Libby, L. A., Noguchi, T., Love, B. C., & Charan Ranganath, A. (2018) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/280362
Cognitive Correlates of Anterolateral Entorhinal Cortex Volume Differences in Older Adults
Yeung, L. (2017) · TSpace (University of Toronto)
Gray matter correlates of progression of motor symptoms in patients with Parkinson’s disease
Pal, P., Naduthota, R., Lenka, A., George, L., Jhunjhunwala, K. R., Saini, J. S., Bharath, R., Christopher, R., Yadav, R., & Gupta, A. (2019) · Annals of Movement Disorders · doi:10.4103/aomd.aomd_8_19
How event-based memories change as a function of forgetting and consolidation
Joensen, B. H. (2019) · White Rose eTheses Online (University of Leeds, The University of Sheffield, University of York)
The role of the anterior and posterior medial temporal lobes in episodic memory and object perception
Snytte, J. (2020) · doi:10.82308/53386
Chinese character unitization enhances recollection-based associative recognition: Evidence from fMRI.
Zhao, C.-Y., Peng, Y.-B., Liu, Z.-J., Wei, P., & Guo, C.-Y. (2023) · PsyCh Journal · doi:10.1002/pchj.663
Anxiety, brain structure and socioeconomic status in middle-aged and older adultsPreprint
Johns, S., Lea‐Carnall, C., Shryane, N. M., & Maharani, A. (2025) · medRxiv · doi:10.1101/2025.04.14.25325776
Neurotransmitter-based machine-learning model for distinguishing Alzheimer’s disease and mild cognitive impairment
Zhao, J., Qu, Z., Li, Z., Zhou, L., Hu, Y., Yu, S., Chen, X., Shu, H., & Initiative, A. D. N. (2026) · Journal of International Medical Research · doi:10.1177/03000605251409886
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Contribution à l’étude de la mémoire épisodique dans la schizophrénie : investigations comportementales et électrophysiologiques de l‘effet du traitement du contenu sémantique des stimuli sur la mobilisation des processus de familiarité et de récupération contextuelle chez des personnes atteintes de schizophrénie
Battal-Merlet, L. (2019) · theses.fr (ABES) · doi:10.70675/7e556f24z8bd5z4c89z8632zb1f371c1f12d
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Coppalle, R. (2020) · theses.fr (ABES) · doi:10.70675/374421dcz7d65z480aza1fcz2a44c1c0f8df
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Dautricourt, S. (2021) · theses.fr (ABES) · doi:10.70675/63472a25z31eaz4ebczaebdzd8d2e061b4b8
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Authors: Diana, R. A., Yonelinas, A. P., & Ranganath, C.
Affiliations: University of California, Davis (US)
ORCID: Diana, Rachel A.
Yonelinas, Andrew P.
Venue: Journal of Cognitive Neuroscience
Publisher: MIT Press
Published: 2010-08-01
Volume: 22
Issue: 8
Pages: 1808-1818
ISSN: 0898-929X (ISSN-L)
1530-8898
DOI: 10.1162/jocn.2009.21335
PMC: PMC2862119
OpenAlex: W2099171807
Cited by: 191
References: 47
Citations by year: 2026: 3 · 2025: 3 · 2024: 8 · 2023: 8 · 2022: 4 · 2021: 7 · 2020: 10 · 2019: 16 · 2018: 14 · 2017: 13 · 2016: 8 · 2015: 18 · 2014: 14 · 2013: 13 · 2012: 22
FWCI: 8.39
Type: journal article
Language: en
Open access: green
www.ncbi.nlm.nih.gov
Locations: Journal of Cognitive Neuroscience (publishedVersion)
PubMed (publishedVersion)
PubMed Central (acceptedVersion)
Funders: National Institutes of Health
University of California, Davis
National Institute of Mental Health (MH079621, K99MH083945, MH059352, MH 068721, R01MH083734, R01MH068721, R01MH059352, F32MH079621)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
Keywords: medial temporal lobe, episodic memory, source memory, recollection, perirhinal cortex, parahippocampal cortex, hippocampus, amnesia, event-related fMRI
MeSH terms: Adult, Amnesia, Brain Mapping, Female, Humans, Image Processing, Computer-Assisted, Magnetic Resonance Imaging, Male, Middle Aged, Neuropsychological Tests, Oxygen, Mental Recall, ROC Curve, Temporal Lobe, Recognition, Psychology

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Medial Temporal Lobe Activity during Source Retrieval Reflects Information Type, not Memory Strength

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