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Space in the brain: how the hippocampal formation supports spatial cognition
Open accessAbstract
Over the past four decades, research has revealed that cells in the hippocampal formation provide an exquisitely detailed representation of an animal's current location and heading. These findings have provided the foundations for a growing understanding of the mechanisms of spatial cognition in mammals, including humans. We describe the key properties of the major categories of spatial cells: place cells, head direction cells, grid cells and boundary cells, each of which has a characteristic firing pattern that encodes spatial parameters relating to the animal's current position and orientation. These properties also include the theta oscillation, which appears to play a functional role in the representation and processing of spatial information. Reviewing recent work, we identify some themes of current research and introduce approaches to computational modelling that have helped to bridge the different levels of description at which these mechanisms have been investigated. These range from the level of molecular biology and genetics to the behaviour and brain activity of entire organisms. We argue that the neuroscience of spatial cognition is emerging as an exceptionally integrative field which provides an ideal test-bed for theories linking neural coding, learning, memory and cognition.
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“Some of these spatial strategies necessarily involve complex learning and memory capabilities and require the concurrence of flexible representational mechanisms, the most remarkable of which probably is allocentric navigation based on map-like spatial memory”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“Such hypothetical memory representations presumably encode the spatial relationships between all the known places and landmarks in a common allocentric reference frame or unitary global map, accessible as a whole, and that can operate to infer the spatial relationships between any of the represented elements.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“The hippocampus of tetrapods seems to be essential in tasks requiring the formation of a memory of the spatial relationships of multiple elements and cues of the environment and those demanding the flexible expression of previously acquired spatial knowledge [72,73,75,76].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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“A considerable amount of evidence shows that the medial pallium or hippocampus of land vertebrates plays a central role in allocentric spatial navigation.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
Experimental — accuracy not yet measuredThe source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
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“For example, in mammals [39,57,72,149], birds [97,98,99,150,151,152,153], and reptiles [112,154,155,156,157], the hippocampal lesions produce impairments on spatial tasks that require the use of map-like or relational spatial memory.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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“Mammalian extra-hippocampal cortical areas contain a variety of functionally specialized neurons with presumably distinct roles in the representation of space, i.e., “head direction cells”, “border cells”, and “grid cells”, that likely encode relevant spatial information in egocentric coordinates [72,193,194,195,196].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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“The tolerance to partial losses of spatial information has been proposed to be a key characteristic of the mammalian hippocampus-dependent map-like spatial memory”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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“The “place cells”, i.e., hippocampal neurons that fire when the animal occupies a particular location of the space, have been proposed to be the higher instance of a brain system that builds up map-like spatial memory representations anchored in the external world, contributing to the neural computations required for allocentric navigation [39,72,74,197,198].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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In the citing paper
“These results closely resemble those obtained after hippocampus lesions in mammals, birds, and reptiles [39,57,72,97,98,112,152,157] and demonstrated that the dorsolateral telencephalon of teleost fish is a critical brain center for allocentric navigation based in map-like spatial memory.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [72]
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Cites
Receptive fields, binocular interaction and functional architecture in the cat’s visual cortex
Hubel, D. H., & Wiesel, T. N. (1962) · The Journal of Physiology · doi:10.1113/jphysiol.1962.sp006837 · Cited by 13,680
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
Self-citationBliss, T. V. P., & Gardner-Medwin, A. R. (1973) · The Journal of Physiology · doi:10.1113/jphysiol.1973.sp010274 · Cited by 7,424
LOSS OF RECENT MEMORY AFTER BILATERAL HIPPOCAMPAL LESIONS
Scoville, W. B., & Milner, B. (1957) · Journal of Neurology, Neurosurgery & Psychiatry · doi:10.1136/jnnp.20.1.11 · Cited by 7,322
Cognitive maps in rats and men
Tolman, E. C. (1948) · Psychological Review · doi:10.1037/h0061626 · Cited by 6,641
Place navigation impaired in rats with hippocampal lesions
Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O'Keefe, J. (1982) · Nature · doi:10.1038/297681a0 · Cited by 6,340
Self-citationThe hippocampus as a spatial map. Preliminary evidence from unit activity in the freely-moving rat
O'Keefe, J., & Dostrovsky, J. (1971) · Brain Research · doi:10.1016/0006-8993(71)90358-1 · Cited by 6,151
Self-citationThe hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
Millisecond-timescale, genetically targeted optical control of neural activity
Boyden, E. S., Zhang, F., Bamberg, E., Nagel, G., & Deisseroth, K. A. (2005) · Nature Neuroscience · doi:10.1038/nn1525 · Cited by 5,015
Buzsáki, G. (2006) · doi:10.1093/acprof:oso/9780195301069.001.0001 · Cited by 4,873
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- Milner AD, 1999, The hippocampal and parietal foundations of spatial cognition, 443
- 10.1113/jphysiol.1973.sp010273 · DOI · Paper page
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Sorted by citations
Items 201–300 of 491
Banker, S. M., Pagliaccio, D., Ramphal, B., Thomas, L. V., Dranovsky, A., & Margolis, A. E. (2020) · Hippocampus · doi:10.1002/hipo.23264 · Cited by 19
Waypoint Path Planning With Synaptic-Dependent Spike Latency
Koul, S., & Horiuchi, T. K. (2019) · IEEE Transactions on Circuits and Systems I Regular Papers · doi:10.1109/tcsi.2018.2882818 · Cited by 18
Network instability dynamics drive a transient bursting period in the developing hippocampus in vivo
Graf, J., Rahmati, V., Majoros, M., Witte, O. W., Geis, C., Kiebel, S. J., Holthoff, K., & Kirmse, K. (2022) · eLife · doi:10.7554/elife.82756 · Cited by 15
Conjunctive encoding of exploratory intentions and spatial information in the hippocampus
Zeng, Y., Yang, K., Cui, Y., Zhu, X., Li, R., Zhang, H., Wu, D., Stevens, R. C., Hu, J., & Zhou, N. (2024) · Nature Communications · doi:10.1038/s41467-024-47570-4 · Cited by 14
The hippocampal CA2 region discriminates social threat from social safety
Kassraian, P., Bigler, S., Suarez, D. M. G., Shrotri, N., Barnett, A., Lee, H., Young, W. S., & Siegelbaum, S. A. (2024) · Nature Neuroscience · doi:10.1038/s41593-024-01771-8 · Cited by 21
The Sensory Neocortex and Associative Memory
Aschauer, D. F., & Rumpel, S. (2016) · Current topics in behavioral neurosciences · doi:10.1007/7854_2016_453 · Cited by 17
Models of spatial and temporal dimensions of memory
Hasselmo, M. E., Hinman, J. R., Dannenberg, H., & Stern, C. E. (2017) · Current Opinion in Behavioral Sciences · doi:10.1016/j.cobeha.2017.05.024 · Cited by 18
Distinct regions of the hippocampus are associated with memory for different spatial locations
Jeye, B. M., MacEvoy, S. P., Karanian, J. M., & Slotnick, S. D. (2018) · Brain Research · doi:10.1016/j.brainres.2018.02.029 · Cited by 16
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Ward, A. R., & Capra, R. (2020) · International ACM SIGIR Conference on Research and Development in Information Retrieval (SIGIR) · doi:10.1145/3397271.3401303 · Cited by 16
Emergent neural dynamics and geometry for generalization in a transitive inference task
Kay, K., Biderman, N., Khajeh, R., Beirán, M., Cueva, C. J., Shohamy, D., Jensen, G., Wei, X.-X., Ferrera, V. P., & Abbott, L. F. (2024) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1011954 · Cited by 18
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Moncayo, R., & Ortner, K. (2015) · BBA Clinical · doi:10.1016/j.bbacli.2015.04.002 · Cited by 16
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Zhao, K., Nie, J., Yang, L., Liu, X., Shang, Z., & Wan, H. (2019) · Brain Research Bulletin · doi:10.1016/j.brainresbull.2019.09.005 · Cited by 14
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Glikmann‐Johnston, Y., Mercieca, E., Carmichael, A. M., Alexander, B., Harding, I. H., & Stout, J. C. (2021) · Journal of Neuroscience Research · doi:10.1002/jnr.24966 · Cited by 15
Pietras, B., Schmutz, V., & Schwalger, T. (2022) · PLoS Computational Biology · doi:10.1371/journal.pcbi.1010809 · Cited by 16
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Pilkiw, M., & Takehara‐Nishiuchi, K. (2018) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2018.03.024 · Cited by 18
Andrianova, L., Banks, P. J., Booth, C. A., Brady, E. S., Margetts‐Smith, G., Kohli, S., Cavanagh, J., Bashir, Z. I., McBain, C. J., & Craig, M. T. (2021) · bioRxiv (Cold Spring Harbor Laboratory) · doi:10.1101/2021.09.30.462517 · Cited by 15
Poos, J. M., van der Ham, I. J. M., Leeuwis, A. E., Pijnenburg, Y. A. L., van der Flier, W. M., & Postma, A. (2021) · Brain Sciences · doi:10.3390/brainsci11101350 · Cited by 14
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Balcells, M. C., Aiello, S., Prat, Q., Andueza, J., Crescimanno, G., & Foguet, O. C. (2020) · Physiology & Behavior · doi:10.1016/j.physbeh.2020.112849 · Cited by 14
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Madl, T., Franklin, S., Chen, K., & Trappl, R. (2017) · Cognitive Systems Research · doi:10.1016/j.cogsys.2017.08.002 · Cited by 16
Schurr, R., Nitzan, M., Eliahou, R., Spinelli, L., Seeck, M., Blanke, O., & Arzy, S. (2018) · Frontiers in Computational Neuroscience · doi:10.3389/fncom.2018.00011 · Cited by 17
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Zhou, D., Cai, Q., Luo, J., Yi, Z., Li, Y., Seger, C. A., & Chen, Q. (2021) · Brain and Cognition · doi:10.1016/j.bandc.2021.105756 · Cited by 14
Ma, X., Zheng, C. Y., Chen, Y., Pereira, F., & Li, Z. (2022) · Cerebral Cortex · doi:10.1093/cercor/bhac205 · Cited by 16
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Kobayashi, K. S., & Matsuo, N. (2023) · Cell Reports · doi:10.1016/j.celrep.2022.111989 · Cited by 13
Yuan, M., & Kennedy, K. M. (2023) · The Journal of Prevention of Alzheimer s Disease · doi:10.14283/jpad.2023.18 · Cited by 13
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Knops, A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-811529-9.00011-x · Cited by 13
Santos, T. B., Wallau, A. E., Soares, J. C. K., & Oliveira, M. G. M. (2020) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2020.107216 · Cited by 14
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Santos, T. B., Soares, J. C. K., Favaro, V. M., & Oliveira, M. G. M. (2017) · Neurobiology of Learning and Memory · doi:10.1016/j.nlm.2017.05.003 · Cited by 13
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Noack, H., Schick, W., Mallot, H., & Born, J. (2017) · Learning & Memory · doi:10.1101/lm.043984.116 · Cited by 12
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Meester, G. D., Linden, L. V., Torfs, J. R. R., Pafilis, P., Šunje, E., Steenssens, D., Zulčić, T., Sassalos, A., & Damme, R. V. (2022) · Evolution · doi:10.1111/evo.14618 · Cited by 12
Li, K., Ma, X., Chen, T., Xin, J., Wang, C., Wu, B., Ogihara, A., Zhou, S., Liu, J., Huang, S., et al. (2023) · Digital Health · doi:10.1177/20552076231194938 · Cited by 12
Newell, A. J., Lalitsasivimol, D., Willing, J., Gonzales, K. L., Waters, E. M., Milner, T. A., McEwen, B. S., & Wagner, C. K. (2018) · The Journal of Comparative Neurology · doi:10.1002/cne.24485 · Cited by 15
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Shao, Q., Wang, Y., Xu, X., Wang, Y., Pan, X., Du, Y., & Wang, R. (2025) · Cognitive Neurodynamics · doi:10.1007/s11571-025-10282-6 · Cited by 9
Serino, S., Stramba-Badiale, C., Magni, G., Castegnaro, A., Riva, G., & Tuena, C. (2025) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2025.106379 · Cited by 10
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Trinh, A.-T., Clarke, S. E., Harvey-Girard, E., & Maler, L. (2019) · doi:10.1101/571414 · Cited by 6
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Metadata
- Authors
- Hartley, T., Lever, C., Burgess, N., & O'Keefe, J.
- Affiliations
- University of York (GB)
- Durham University (GB)
- UCL Queen Square Institute of Neurology (GB)
- Sainsbury Wellcome Centre (GB)
- Venue
- Philosophical Transactions of the Royal Society B: Biological Sciences
- Publisher
- The Royal Society
- Published
- 2014-02-05
- Volume
- 369
- Issue
- 1635
- Pages
- 20120510
- ISSN
- 0962-8436 (ISSN-L)
- 1471-2970
- PMC
- PMC3866435
- OpenAlex
- W2146561158
- Cited by
- 495
- References
- 219
- Citations by year
- 2026: 23 · 2025: 43 · 2024: 32 · 2023: 30 · 2022: 41 · 2021: 45 · 2020: 41 · 2019: 44 · 2018: 38 · 2017: 56 · 2016: 42 · 2015: 45 · 2014: 15
- FWCI
- 2.90
- Type
- journal article
- Language
- en
- Open access
- bronze
- doi.org
- Locations
- Philosophical Transactions of the Royal Society B Biological Sciences (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- White Rose Research Online (University of Leeds, The University of Sheffield, University of York) (submittedVersion)
- UCL Discovery (University College London) (submittedVersion)
- Durham Research Online (Durham University) (submittedVersion, cc-by)
- Funders
- Wellcome Trust (095811)
- Medical Research Council
- Biotechnology and Biological Sciences Research Council (BB/G01342X/2, BB/G01342X/1)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Developmental Neuroscience › Neurogenesis and neuroplasticity mechanisms
- Keywords
- hippocampal formation, spatial cognition, place cells, head direction cells, grid cells, boundary cells, theta oscillations, spatial representation, neural coding, computational modelling, memory, learning
- MeSH terms
- Action Potentials, Animals, Cognition, Computer Simulation, Hippocampus, Humans, Models, Neurological, Neurons, Space Perception, Theta Rhythm, Mice, Rats
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