Medial temporal lobe activity during complex discrimination of faces, objects, and scenes: Effects of viewpoint
Open accessAbstract
The medial temporal lobe (MTL), a set of heavily interconnected structures including the hippocampus and underlying entorhinal, perirhinal and parahippocampal cortex, is traditionally believed to be part of a unitary system dedicated to declarative memory. Recent studies, however, demonstrated perceptual impairments in amnesic individuals with MTL damage, with hippocampal lesions causing scene discrimination deficits, and perirhinal lesions causing object and face discrimination deficits. The degree of impairment on these tasks was influenced by the need to process complex conjunctions of features: discriminations requiring the integration of multiple visual features caused deficits, whereas discriminations that could be solved on the basis of a single feature did not. Here, we address these issues with functional neuroimaging in healthy participants as they performed a version of the oddity discrimination task used previously in patients. Three different types of stimuli (faces, scenes, novel objects) were presented from either identical or different viewpoints. Consistent with studies in patients, we observed increased perirhinal activity when participants distinguished between faces and objects presented from different, compared to identical, viewpoints. The posterior hippocampus, by contrast, showed an effect of viewpoint for both faces and scenes. These findings provide convergent evidence that the MTL is involved in processes beyond long‐term declarative memory and suggest a critical role for these structures in integrating complex features of faces, objects, and scenes into view‐invariant, abstract representations. © 2009 Wiley‐Liss, Inc.
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Tzourio-Mazoyer, N., Landeau, B., Papathanassiou, D., Crivello, F., Etard, O., Delcroix, N., Mazoyer, B., & Joliot, M. (2002) · NeuroImage · doi:10.1006/nimg.2001.0978 · Cited by 16,319 · see citing works
Statistical parametric maps in functional imaging: A general linear approach
Friston, K. J., Holmes, A. P., Worsley, K. J., Poline, J. ‐., Frith, C. D., & Frackowiak, R. S. J. (1994) · Human Brain Mapping · doi:10.1002/hbm.460020402 · Cited by 9,688 · see citing works
The fusiform face area: a module in human extrastriate cortex specialized for face perception
Kanwisher, N., McDermott, J., & Chun, M. M. (1997) · The Journal of Neuroscience · doi:10.1523/jneurosci.17-11-04302.1997 · Cited by 7,738 · see citing works
A cortical representation of the local visual environment
Epstein, R. A., & Kanwisher, N. (1998) · Nature · doi:10.1038/33402 · Cited by 2,960 · see citing works
Squire, L. R., Stark, C. E. L., & Clark, R. E. (2004) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.27.070203.144130 · Cited by 2,680 · see citing works
Common regions of the human frontal lobe recruited by diverse cognitive demands
Duncan, J., & Owen, A. M. (2000) · Trends in Neurosciences · doi:10.1016/s0166-2236(00)01633-7 · Cited by 2,498 · see citing works
Event-Related fMRI: Characterizing Differential Responses
Friston, K. J., Fletcher, P. C., Josephs, O., Holmes, A., Rugg, M. D., & Turner, R. (1998) · NeuroImage · doi:10.1006/nimg.1997.0306 · Cited by 2,017 · see citing works
Episodic memory, amnesia, and the hippocampal–anterior thalamic axis
Aggleton, J. P., & Brown, M. W. (1999) · Behavioral and Brain Sciences · doi:10.1017/s0140525x99002034 · Cited by 1,879 · see citing works
Two functional components of the hippocampal memory system
Eichenbaum, H., Otto, T., & Cohen, N. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035391 · Cited by 1,094 · see citing works
Becoming a “Greeble” Expert: Exploring Mechanisms for Face Recognition
Gauthier, L., & Tarr, M. J. (1997) · Vision Research · doi:10.1016/s0042-6989(96)00286-6 · Cited by 1,017 · see citing works
Recognition memory and the medial temporal lobe: a new perspective
Squire, L. R., Wixted, J. T., & Clark, R. E. (2007) · Nature reviews. Neuroscience · doi:10.1038/nrn2154 · Cited by 1,013 · see citing works
Classical and Bayesian Inference in Neuroimaging: Theory
Friston, K. J., Penny, W. D., Phillips, C. L. M., Kiebel, S. J., Hinton, G. E., & Ashburner, J. (2002) · NeuroImage · doi:10.1006/nimg.2002.1090 · Cited by 597 · see citing works
Winters, B. D., Forwood, S., Cowell, R. A., Saksida, L. M., & Bussey, T. J. (2004) · Journal of Neuroscience · doi:10.1523/jneurosci.1346-04.2004 · Cited by 588 · see citing works
Memory deficits for implicit contextual information in amnesic subjects with hippocampal damage
Chun, M. M., & Phelps, E. A. (1999) · Nature Neuroscience · doi:10.1038/12222 · Cited by 554 · see citing works
Cabeza, R. E. L., Dolcos, F., Graham, R., & Nyberg, L. H. (2002) · NeuroImage · doi:10.1006/nimg.2002.1063 · Cited by 466 · see citing works
The Long and the Short of It: Relational Memory Impairments in Amnesia, Even at Short Lags
Hannula, D. E., Tranel, D., & Cohen, N. J. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.5222-05.2006 · Cited by 436 · see citing works
Working Memory for Conjunctions Relies on the Medial Temporal Lobe
Olson, I. R., Page, K., Moore, K., Chatterjee, A., & Verfaellie, M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1923-05.2006 · Cited by 426 · see citing works
Medial Temporal Lobe Activity Associated with Active Maintenance of Novel Information
Charan Ranganath, A., & D’Esposito, M. (2001) · Neuron · doi:10.1016/s0896-6273(01)00411-1 · Cited by 391 · see citing works
Perirhinal cortex resolves feature ambiguity in complex visual discriminations
Bussey, T., Saksida, L., & Murray, E. A. (2002) · European Journal of Neuroscience · doi:10.1046/j.0953-816x.2001.01851.x · Cited by 365 · see citing works
The hippocampus is required for short‐term topographical memory in humans
Hartley, T., Bird, C. M., Chan, D., Cipolotti, L., Husain, M., Vargha‐Khadem, F., & Burgess, N. (2006) · Hippocampus · doi:10.1002/hipo.20240 · Cited by 349 · see citing works
An Unexpected Sequence of Events: Mismatch Detection in the Human Hippocampus
Kumaran, D., & Maguire, E. A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040424 · Cited by 324 · see citing works
Perceptual deficits in amnesia: challenging the medial temporal lobe ‘mnemonic’ view
Lee, A. C. H., Bussey, T. J., Murray, E. A., Saksida, L. M., Epstein, R. A., Kapur, N., Hodges, J. R., & Graham, K. S. (2004) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.07.017 · Cited by 308 · see citing works
Self-citationSpecialization in the medial temporal lobe for processing of objects and scenes
Lee, A. C. H., Buckley, M. J., Pegman, S. J., Spiers, H. J., Scahill, V. L., Gaffan, D., Bussey, T. J., Davies, R., Kapur, N., Hodges, J. R., et al. (2005) · Hippocampus · doi:10.1002/hipo.20101 · Cited by 300 · see citing works
Self-citationEffect of unitization on associative recognition in amnesia
Quamme, J., Yonelinas, A., & Norman, K. A. (2007) · Hippocampus · doi:10.1002/hipo.20257 · Cited by 297 · see citing works
The human medial temporal lobe processes online representations of complex objects
Barense, M. D., Gaffan, D., & Graham, K. S. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.05.023 · Cited by 279 · see citing works
Self-citationMatch–Mismatch Processes Underlie Human Hippocampal Responses to Associative Novelty
Kumaran, D., & Maguire, E. A. (2007) · Journal of Neuroscience · doi:10.1523/jneurosci.1677-07.2007 · Cited by 264 · see citing works
Mayes, A. R., Holdstock, J. S., Isaac, C. L., Hunkin, N. M., & Roberts, N. P. (2002) · Hippocampus · doi:10.1002/hipo.1111 · Cited by 262 · see citing works
Hollingworth, A., Richard, A. M., & Luck, S. J. (2008) · Journal of Experimental Psychology General · doi:10.1037/0096-3445.137.1.163 · Cited by 257 · see citing works
Selective Perceptual Impairments After Perirhinal Cortex Ablation
Buckley, M. J., Booth, M. C. A., Rolls, E. T., & Gaffan, D. (2001) · Journal of Neuroscience · doi:10.1523/jneurosci.21-24-09824.2001 · Cited by 249 · see citing works
Functional Specialization in the Human Medial Temporal Lobe
Barense, M. D., Bussey, T. J., Lee, A. C. H., Rogers, T. T., Davies, R., Saksida, L. M., Murray, E. A., & Graham, K. S. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.2704-05.2005 · Cited by 233 · see citing works
Self-citationVisual Working Memory Is Impaired when the Medial Temporal Lobe Is Damaged
Olson, I. R., Moore, K. S., Stark, M., & Chatterjee, A. K. (2006) · Journal of Cognitive Neuroscience · doi:10.1162/jocn.2006.18.7.1087 · Cited by 221 · see citing works
Recognition memory for faces: When familiarity supports associative recognition judgments
Yonelinas, A., Kroll, N., Dobbins, I., & Soltani, M. (1999) · Psychonomic Bulletin & Review · doi:10.3758/bf03212975 · Cited by 204 · see citing works
Retrograde amnesia after hippocampal damage: Recent vs. remote memories in two tasks
Sutherland, R. J., Weisend, M. P., Mumby, D. G., Astur, R. S., Hanlon, F. M., Koerner, A., Thomas, M. J., Wu, Y., Moses, S. N., Cole, C., et al. (2001) · Hippocampus · doi:10.1002/1098-1063(2001)11:1 · Cited by 190 · see citing works
Nichols, E. A., Kao, Y.-C., Verfaellie, M. H., & Gabrieli, J. D. E. (2006) · Hippocampus · doi:10.1002/hipo.20190 · Cited by 180 · see citing works
Pihlajamäki, M., Tanila, H., Könönen, M., Hänninen, T., Hämäläinen, A., Soininen, H., & Aronen, H. (2004) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2004.03282.x · Cited by 156 · see citing works
Activating the medial temporal lobe during oddity judgment for faces and scenes.
Lee, A. C. H., Scahill, V., & Graham, K. (2008) · Cerebral Cortex · doi:10.1093/cercor/bhm104 · Cited by 154 · see citing works
Self-citationWorking Memory for Complex Scenes: Age Differences in Frontal and Hippocampal Activations
Park, D. C., Welsh, R. C., Marshuetz, C., Gutchess, A. H., Mikels, J. A., Polk, T. A., Noll, D. C., & Taylor, S. F. (2003) · Journal of Cognitive Neuroscience · doi:10.1162/089892903322598094 · Cited by 150 · see citing works
Lee, A. C. H., Buckley, M. J., Gaffan, D., Emery, T., Hodges, J. R., & Graham, K. S. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.3157-05.2006 · Cited by 147 · see citing works
Self-citationThe contribution of familiarity to associative memory in amnesia.
Giovanello, K., Keane, M., & Verfaellie, M. (2006) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2006.03.004 · Cited by 143 · see citing works
Working Memory and the Organization of Brain Systems
Shrager, Y., Levy, D. A., Hopkins, R. O., & Squire, L. R. (2008) · The Journal of Neuroscience · doi:10.1523/jneurosci.0710-08.2008 · Cited by 123 · cited 2× · see citing works
“…of short-term memory for stimulus conjunctions in amnesia (Hannula et al., 2006; Nichols et al., 2006; Olson et al., 2006a,b, although see Shrager et al., 2008), and fMRI studies have observed hippocampal activity in tasks typically considered to assess short-term memory (Ranganath and…”
The Dynamics of Hippocampal Activation during Encoding of Overlapping Sequences
Kumaran, D., & Maguire, E. A. (2006) · Neuron · doi:10.1016/j.neuron.2005.12.024 · Cited by 120 · see citing works
Category-specificity in the Human Medial Temporal Lobe Cortex
Litman, L., Awipi, T., & Davachi, L. (2009) · Hippocampus · doi:10.1002/hipo.20515 · Cited by 117 · see citing works
Abnormal Categorization and Perceptual Learning in Patients with Hippocampal Damage
Graham, K. S., Scahill, V. L., Hornberger, M., Barense, M. D., Lee, A. C. H., Bussey, T. J., & Saksida, L. M. (2006) · Journal of Neuroscience · doi:10.1523/jneurosci.1535-06.2006 · Cited by 105 · see citing works
Self-citationPerirhinal Contributions to Human Visual Perception
Devlin, J. T., & Price, C. J. (2007) · Current Biology · doi:10.1016/j.cub.2007.07.066 · Cited by 102 · see citing works
Taylor, K. J., Henson, R. N., & Graham, K. S. (2007) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2007.04.004 · Cited by 100 · see citing works
Self-citationHippocampal activations during encoding and retrieval in a verbal working memory paradigm
Karlsgodt, K. H., Shirinyan, D., van Erp, T. G. M., Cohen, M. S., & Cannon, T. D. (2005) · NeuroImage · doi:10.1016/j.neuroimage.2005.01.038 · Cited by 97 · see citing works
Perirhinal cortex activity during visual object discrimination: An event-related fMRI study
Lee, A. C. H., Bandelow, S., Schwarzbauer, C., Henson, R. N., & Graham, K. S. (2006) · NeuroImage · doi:10.1016/j.neuroimage.2006.06.021 · Cited by 61 · see citing works
Self-citationSaksida, L. M., Bussey, T. J., Buckmaster, C. A., & Murray, E. A. (2006) · Hippocampus · doi:10.1002/hipo.20170 · Cited by 59 · see citing works
Activation and Elaboration Effects in Recognition and Word Priming
Mandler, G., Graf, P., & Kraft, D. (1986) · The Quarterly Journal of Experimental Psychology Section A · doi:10.1080/14640748608401618 · Cited by 50 · see citing works
Worsley (1996) · doi:10.1002/(sici)1097-0193(1996)4:1
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Boccia, M., Piccardi, L., & Guariglia, P. (2015) · BioMed Research International · doi:10.1155/2015/419808 · Cited by 187 · see citing works
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- Authors
- Barense, M. D., Henson, R. N. A., Lee, A. C. H., & Graham, K. S.
- Affiliations
- University of Toronto (CA)
- MRC Cognition and Brain Sciences Unit (GB)
- University of Oxford (GB)
- Cardiff University (GB)
- Corresponding author
- Barense, Morgan D.
- Venue
- Hippocampus
- Publisher
- Wiley
- Published
- 2009-06-04
- Volume
- 20
- Issue
- 3
- Pages
- 389-401
- ISSN
- 1050-9631 (ISSN-L)
- 1098-1063
- PMC
- PMC2912509
- OpenAlex
- W2161210141
- Cited by
- 177
- References
- 50
- Citations by year
- 2026: 5 · 2025: 12 · 2024: 8 · 2023: 11 · 2022: 8 · 2021: 9 · 2020: 7 · 2019: 14 · 2018: 7 · 2017: 6 · 2016: 11 · 2015: 16 · 2014: 10 · 2013: 15 · 2012: 18
- FWCI
- 6.13
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Hippocampus (publishedVersion)
- PubMed (publishedVersion)
- PubMed Central (acceptedVersion)
- TSpace (University of Toronto) (submittedVersion)
- Funders
- Wellcome Trust (082315)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Face Recognition and Perception
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- medial temporal lobe, face discrimination, object discrimination, viewpoints, perirhinal cortex, posterior hippocampus, feature integration, view-invariant representation, amnesia, declarative memory
- MeSH terms
- Adolescent, Adult, Brain Mapping, Face, Female, Hippocampus, Humans, Functional Laterality, Magnetic Resonance Imaging, Male, Memory, Neuropsychological Tests, Orientation, Pattern Recognition, Visual, Photic Stimulation, Space Perception, Parahippocampal Gyrus, Recognition, Psychology, Young Adult
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