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Space and time in the brain
Open accessAbstract
Nothing is more intuitive, yet more complex, than the concepts of space and time. In contrast to spacetime in physics, space and time in neuroscience remain separate coordinates to which we attach our observations. Investigators of navigation and memory relate neuronal activity to position, distance, time point, and duration and compare these parameters to units of measuring instruments. Although spatial-temporal sequences of brain activity often correlate with distance and duration measures, these correlations may not correspond to neuronal representations of space or time. Neither instruments nor brains sense space or time. Neuronal activity can be described as a succession of events without resorting to the concepts of space or time. Instead of searching for brain representations of our preconceived ideas, we suggest investigating how brain mechanisms give rise to inferential, model-building explanations.
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“Treating space as a sequence is a necessity for humans and other animals because they lack a global positioning system that enables direct sensing of location coordinates.”
From Space is a latent sequence: A theory of the hippocampus (2024) · cites this paper as [9]
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“However, anomalies have been accumulating over the simple view that place cells represent just locations (8, 9, 32, 45, 46).”
From Space is a latent sequence: A theory of the hippocampus (2024) · cites this paper as [9]
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Citations
Cites
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
Remembering the past to imagine the future: the prospective brain
Schacter, D. L., Addis, D. R., & Buckner, R. L. (2007) · Nature Reviews Neuroscience · doi:10.1038/nrn2213 · Cited by 2,394
The organization of recent and remote memories
Frankland, P. W., & Bontempi, B. (2005) · Nature Reviews Neuroscience · doi:10.1038/nrn1607 · Cited by 2,138
A theory of magnitude: common cortical metrics of time, space and quantity
Walsh, V. (2003) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2003.09.002 · Cited by 2,044
Memory consolidation, retrograde amnesia and the hippocampal complex
Nadel, L., & Moscovitch, M. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80010-4 · Cited by 1,924
Memory, navigation and theta rhythm in the hippocampal-entorhinal system
Buzsáki, G., & Moser, E. I. (2013) · Nature Neuroscience · doi:10.1038/nn.3304 · Cited by 1,847
Self-citationHippocampal sharp wave-ripple: A cognitive biomarker for episodic memory and planning
Buzsáki, G. (2015) · Hippocampus · doi:10.1002/hipo.22488 · Cited by 1,759
Self-citationThe Normalization Model of Attention
Reynolds, J. H., & Heeger, D. J. (2009) · Neuron · doi:10.1016/j.neuron.2009.01.002 · Cited by 1,457
Patients with hippocampal amnesia cannot imagine new experiences
Hassabis, D., Kumaran, D., Vann, S. D., & Maguire, E. A. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610561104 · Cited by 1,414
Unilateral Neglect of Representational Space
Bisiach, E., & Luzzatti, C. (1978) · Cortex · doi:10.1016/s0010-9452(78)80016-1 · Cited by 1,390
Internally Generated Cell Assembly Sequences in the Rat Hippocampus
Pastalkova, E., Itskov, V., Amarasingham, A., & Buzsáki, G. (2008) · Science · doi:10.1126/science.1159775 · Cited by 1,301
Self-citationTime and the observer: The where and when of consciousness in the brain
Dennett, D. C., & Kinsbourne, M. (1992) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00068229 · Cited by 1,032
Choice-specific sequences in parietal cortex during a virtual-navigation decision task
Harvey, C. D., Coen, P., & Tank, D. W. (2012) · Nature · doi:10.1038/nature10918 · Cited by 951
Deciphering The Hippocampal Polyglot: the Hippocampus as a Path Integration System
McNaughton, B. L., Barnes, C. A., Gerrard, J. L., Gothard, K. M., Jung, M. W., Knierim, J. J., Kudrimoti, H. S., Qin, Y., Skaggs, W. E., Suster, M. S., et al. (1996) · Journal of Experimental Biology · doi:10.1242/jeb.199.1.173 · Cited by 914
Critical role of the hippocampus in memory for sequences of events
Fortin, N. J., Agster, K. L., & Eichenbaum, H. B. (2002) · Nature Neuroscience · doi:10.1038/nn834 · Cited by 881
The hippocampal memory indexing theory.
Teyler, T. J., & DiScenna, P. (1986) · Behavioral Neuroscience · doi:10.1037/0735-7044.100.2.147 · Cited by 871
Time cells in the hippocampus: a new dimension for mapping memories
Eichenbaum, H. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3827 · Cited by 843
Mapping of a non-spatial dimension by the hippocampal-entorhinal circuit
Aronov, D., Nevers, R., & Tank, D. W. (2017) · Nature · doi:10.1038/nature21692 · Cited by 773
Toward a neurobiology of temporal cognition: advances and challenges
Gibbon, J., Malapani, C., Dale, C. L., & Gallistel, C. R. (1997) · Current Opinion in Neurobiology · doi:10.1016/s0959-4388(97)80005-0 · Cited by 771
Behavior-dependent short-term assembly dynamics in the medial prefrontal cortex
Fujisawa, S., Amarasingham, A., Harrison, M. T., & Buzsáki, G. (2008) · Nature Neuroscience · doi:10.1038/nn.2134 · Cited by 701
Self-citationCan We Reconcile the Declarative Memory and Spatial Navigation Views on Hippocampal Function?
Eichenbaum, H., & Cohen, N. J. (2014) · Neuron · doi:10.1016/j.neuron.2014.07.032 · Cited by 654
Properties of the Internal Clocka
Church, R. M. (1984) · Annals of the New York Academy of Sciences · doi:10.1111/j.1749-6632.1984.tb23459.x · Cited by 541
Influence of the thalamus on spatial visual processing in frontal cortex
Sommer, M. A., & Wurtz, R. H. (2006) · Nature · doi:10.1038/nature05279 · Cited by 520
Multimodal integration for the representation of space in the posterior parietal cortex
Andersen, R. A. (1997) · Philosophical Transactions of the Royal Society of London. Series B: Biological Sciences · doi:10.1098/rstb.1997.0128 · Cited by 515
I of the Vortex: From Neurons to Self
Llinás, R. R. (2000) · Cited by 479
Self-citationI of the Vortex: From Neurons to Self
Llinás, R. R. (2001) · doi:10.7551/mitpress/3626.001.0001 · Cited by 469
Self-citationHead direction cells and the neurophysiological basis for a sense of direction
Taube, J. S. (1998) · Progress in Neurobiology · doi:10.1016/s0301-0082(98)00004-5 · Cited by 468
Saccadic eye movements cause compression of time as well as space
Morrone, M. C., Ross, J., & Burr, D. C. (2005) · Nature Neuroscience · doi:10.1038/nn1488 · Cited by 439
The case of K.C.: contributions of a memory-impaired person to memory theory
Rosenbaum, R. S., Köhler, S., Schacter, D. L., Moscovitch, M., Westmacott, R., Black, S. E., Gao, F., & Tulving, E. (2005) · Neuropsychologia · doi:10.1016/j.neuropsychologia.2004.10.007 · Cited by 433
Grid cells and cortical representation
Moser, E. I., Roudi, Y., Witter, M. P., Kentros, C., Bonhoeffer, T., & Moser, M.-B. (2014) · Nature Reviews Neuroscience · doi:10.1038/nrn3766 · Cited by 335
Theta sequences are essential for internally generated hippocampal firing fields
Wang, Y., Romani, S., Lustig, B. R., Leonardo, A. M., & Pastalkova, E. (2014) · Nature Neuroscience · doi:10.1038/nn.3904 · Cited by 322
Motor and representational framing of space
Paillard, J. (1991) · doi:10.1093/oso/9780198542841.003.0010 · Cited by 321
Sinha, C., Sinha, V. D. S., Zinken, J., & Sampaio, W. B. D. A. (2011) · Language and Cognition · doi:10.1515/langcog.2011.006 · Cited by 306
During Running in Place, Grid Cells Integrate Elapsed Time and Distance Run
Kraus, B. J., Brandon, M. P., Robinson, R. J., Connerney, M. A., Hasselmo, M. E., & Eichenbaum, H. (2015) · Neuron · doi:10.1016/j.neuron.2015.09.031 · Cited by 294
Hippocampal place cell assemblies are speed-controlled oscillators
Geisler, C. E., Robbe, D., Zugaro, M., Sirota, A., & Buzsáki, G. (2007) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.0610121104 · Cited by 286
Self-citationSense of body and sense of action both contribute to self-recognition
van den Bos, E., & Jeannerod, M. (2002) · Cognition · doi:10.1016/s0010-0277(02)00100-2 · Cited by 271
Time and the Brain: How Subjective Time Relates to Neural Time
Eagleman, D. M., Tse, P. U., Buonomano, D. V., Janssen, P., Nobre, A. C., & Holcombe, A. O. (2005) · Journal of Neuroscience · doi:10.1523/jneurosci.3487-05.2005 · Cited by 238
Visual Perception of Direction for Stimuli Flashed During Voluntary Saccadic Eye Movements
Matin, L., & Pearce, D. G. (1965) · Science · doi:10.1126/science.148.3676.1485 · Cited by 217
The Functional Anatomy of Time: What and When in the Brain
Friston, K. J., & Buzsáki, G. (2016) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2016.05.001 · Cited by 192
Self-citationTemporal and Rate Coding for Discrete Event Sequences in the Hippocampus
Terada, S., Sakurai, Y., Nakahara, H., & Fujisawa, S. (2017) · Neuron · doi:10.1016/j.neuron.2017.05.024 · Cited by 186
Phenomenological Space-Time: Toward an Experiential Relativity
DeLong, A. J. (1981) · Science · doi:10.1126/science.7256273 · Cited by 139
REVIEW ■ : Multiple Representations of Space in the Brain
Gross, C. G., & Graziano, M. S. A. (1995) · The Neuroscientist · doi:10.1177/107385849500100107 · Cited by 118
Learning and remembering real-world events after medial temporal lobe damage
Dede, A. J. O., Frascino, J. C., Wixted, J. T., & Squire, L. R. (2016) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.1617025113 · Cited by 106
Finnerty, G. T., Shadlen, M. N., Jazayeri, M., Nobre, A. C., & Buonomano, D. V. (2015) · Journal of Neuroscience · doi:10.1523/jneurosci.2654-15.2015 · Cited by 102
Emergence of Cognition from ActionPreprint
Buzsáki, G., Peyrache, A., & Kubie, J. L. (2014) · Cold Spring Harbor Symposia on Quantitative Biology · doi:10.1101/sqb.2014.79.024679 · Cited by 86
Self-citationBonasia, K., Blommesteyn, J., & Moscovitch, M. (2016) · Hippocampus · doi:10.1002/hipo.22539 · Cited by 84
A Neural Model of the Cortical Representation of Egocentric Distance
Pouget, A., & B, T. J. S. A. (1994) · Cerebral Cortex · doi:10.1093/cercor/4.3.314 · Cited by 82
Rovelli, C. (2014) · Cited by 81
Corollary Discharge and Oculomotor Proprioception: Cortical Mechanisms for Spatially Accurate Vision
Sun, L. D., & Goldberg, M. E. (2016) · Annual Review of Vision Science · doi:10.1146/annurev-vision-082114-035407 · Cited by 75
Dysfunctional counting of mental time in Parkinson’s disease
Honma, M., Kuroda, T., Futamura, A., Shiromaru, A., & Kawamura, M. (2016) · Scientific Reports · doi:10.1038/srep25421 · Cited by 47
Amaral, D. G., Lavenex, P., & Insausti, R. (2025) · Oxford University Press eBooks · doi:10.1093/med/9780190065324.003.0003 · Cited by 24
Muller, R. A. (2016) · International Linear Collider · Cited by 17
Nitz, D. A. (2014) · Springer eBooks · doi:10.1007/978-3-7091-1292-2_2 · Cited by 4
Research works printed but not linked: 4
- E. C. Traugott “On the expression of spatio-temporal relations in language” in Universals of Human Language III J. H. Greenberg C. A. Ferguson E. A. Moravcsik Eds. (Stanford Univ. Press 1978) pp. 369–400.
- J. O’Keefe L. Nadel The Hippocampus as a Cognitive Map (Oxford Univ. Press 1978).
- H. Bergson Duration and Simultaneity R. Durie Ed. (Clinamen Press 1999).
- K. S. Lashley “The problem of serial order in behavior” in Cerebral Mechanisms in Behavior L. A. Jeffress Ed. (Wiley 1951) pp. 112–136.
Cited by
Sorted by citations
Viewpoints: how the hippocampus contributes to memory, navigation and cognition
Lisman, J., Buzsáki, G., Eichenbaum, H., Nadel, L., Ranganath, C., & Redish, A. D. (2017) · Nature Neuroscience · doi:10.1038/nn.4661 · Cited by 851
Self-citationSpace and Time: The Hippocampus as a Sequence Generator
Buzsáki, G., & Tingley, D. (2018) · Trends in Cognitive Sciences · doi:10.1016/j.tics.2018.07.006 · Cited by 461
“If distance and duration are defined and understood with the help of human-made measuring instruments, one may wonder how space and time are computed and comprehended by other animals who cannot read those instruments [9].”
BackgroundInfluentialSelf-citationIntegrating time from experience in the lateral entorhinal cortex
Tsao, A., Sugar, J., Lu, L., Wang, C., Knierim, J. J., Moser, M.-B., & Moser, E. I. (2018) · Nature · doi:10.1038/s41586-018-0459-6 · Cited by 490
The Neural Basis of Timing: Distributed Mechanisms for Diverse Functions
Paton, J. J., & Buonomano, D. V. (2018) · Neuron · doi:10.1016/j.neuron.2018.03.045 · Cited by 469
“It is increasingly well accepted that the ability to tell time, to predict when events will happen, and to process and represent temporal patterns are among the brain’s most important and basic functions (Meck and Ivry, 2016; Buzsáki and Llinás, 2017).”
BackgroundNorthoff, G., Wainio‐Theberge, S., & Evers, K. (2019) · Physics of Life Reviews · doi:10.1016/j.plrev.2019.05.002 · Cited by 272
Metadata
- Authors
- Buzsáki, G., & Llinás, R.
- Affiliations
- New York University (US)
- Corresponding author
- Buzsáki, György
- ORCID
- Buzsáki, György
- Venue
- Science
- Published
- 2017-10-27
- Volume
- 358
- Issue
- 6362
- Pages
- 482-485
- ISSN
- 0036-8075 (ISSN-L)
- 1095-9203
- PMC
- PMC5998813
- OpenAlex
- W2766264103
- Semantic Scholar
- 492d4fdcadcc502d185bd3924176dbf422cf451a
- Cited by
- 175
- References
- 53
- Citations by year
- 2026: 8 · 2025: 13 · 2024: 19 · 2023: 18 · 2022: 17 · 2021: 32 · 2020: 25 · 2019: 23 · 2018: 16 · 2017: 1
- FWCI
- 1.97
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Science (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Funders
- National Institutes of Health (award343774, NS 090583, award343775, NS090526, award343777, NS074015)
- National Institute of Mental Health (award343773, MH54671)
- Simons Foundation (award343778)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural dynamics and brain function
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
- Keywords
- spatial representation, representation of time, neuronal activity, navigation, memory, model development, inference
- MeSH terms
- Animals, Brain, Humans, Neurons, Space Perception, Time Perception, Rats, Memory, Episodic, Spatial Navigation
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