The cognitive map as a hippocampus
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
The dorsolateral telencephalon of teleost fish is a critical brain center for allocentric navigation based on map-like spatial memory.
“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 [39]
Such hypothetical memory representations presumably encode the spatial relationships between all known places and landmarks in a common allocentric reference frame or unitary global map, accessible as a whole, and can operate to infer spatial relationships between any represented elements.
“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 [39]
Some teleost spatial strategies necessarily involve complex learning and memory capabilities and require flexible representational mechanisms, the most remarkable of which is allocentric navigation based on map-like spatial memory.
“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 [39]
As a whole, these results indicate that teleost fish, like mammals, birds, and reptilians, can use allocentric strategies to solve spatial tasks.
“As a whole, these results indicate that teleost fish, like mammals [39,48,65,68,96], birds [97,98,99,100], and reptilians [101,102], can use allocentric strategies to solve spatial tasks.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [39]
Tolerance to partial losses of spatial information has been proposed to be a key characteristic of mammalian hippocampus-dependent map-like spatial memory.
“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 [39]
Shortcutting and detouring behavior has been proposed as key evidence to distinguish allocentric navigation based on cognitive maps or survey representations from more simple navigational strategies.
“shortcutting and detouring behavior has been proposed as a key evidence to distinguish allocentric navigation based on cognitive maps or survey representations from more simple navigational strategies”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [39]
This inferential capability allows animals to plan their paths and to undertake flexible and purposive navigational responses.
“This inferential capability allows the animals to plan their paths and to undertake flexible and purposive navigational responses.”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [39]
The cognitive map view proposes that animals do not merely respond reflexively to cue stimuli, but instead acquire meaningful information about spatial relationships in the environment, enabling them to make inferences about how places are connected through unknown terrains.
“The cognitive map view proposes that the animals do not merely respond reflexively to the cue stimuli, but instead they acquire meaningful information about the spatial relationships in the environment, which enable them to make inferences (or to form “expectations”) about how places are connected through unknown terrains”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [39]
The medial pallium or hippocampus of land vertebrates plays a central role in allocentric spatial navigation.
“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 [39]
Hippocampal lesions in mammals, birds, and reptiles produce impairments on spatial tasks that require the use of map-like or relational spatial memory.
“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 [39]
Place cells, hippocampal neurons that fire when the animal occupies a particular location, are proposed as the higher instance of a brain system that builds map-like spatial memory representations anchored in the external world, contributing to allocentric navigation.
“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 [39]
Cites
Cognitive maps in rats and men
Tolman, E. C. (1948) · Psychological Review · doi:10.1037/h0061626 · Cited by 6,641 · see citing works
Simple memory: a theory for archicortex
Marr, D. (1971) · Philosophical Transactions of the Royal Society of London. B, Biological Sciences · doi:10.1098/rstb.1971.0078 · Cited by 2,771 · see citing works
Mountcastle, V. B., Lynch, J. C., Georgopoulos, A., Sakata, H., & Acuna, C. (1975) · Journal of Neurophysiology · doi:10.1152/jn.1975.38.4.871 · Cited by 2,061 · see citing works
Preliminary analysis of functions of the temporal lobes in monkeys
KLÜVER, H. (1939) · Archives of Neurology And Psychiatry · doi:10.1001/archneurpsyc.1939.02270240017001 · Cited by 1,696 · see citing works
THE NEUROANATOMY OF AMNESIA: A CRITIQUE OF THE HIPPOCAMPAL MEMORY HYPOTHESIS
HOREL, J. A. (1978) · Brain · doi:10.1093/brain/101.3.403 · Cited by 493 · see citing works
Solomon, P. R., & Moore, J. W. (1975) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077183 · Cited by 473 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Cultural neuroscience of the self: understanding the social grounding of the brain
Kitayama, S., & Park, J. (2010) · Social Cognitive and Affective Neuroscience · doi:10.1093/scan/nsq052 · Cited by 335 · see citing works
Solving the detour problem in navigation: a model of prefrontal and hippocampal interactions
Spiers, H. J., & Gilbert, S. J. (2015) · Frontiers in Human Neuroscience · doi:10.3389/fnhum.2015.00125 · Cited by 94 · see citing works
Spatial Cognition in Teleost Fish: Strategies and Mechanisms
Rodríguez, F., Quintero, B., Amores, L., Madrid, D., Salas-Peña, C., & Salas, C. (2021) · Animals · doi:10.3390/ani11082271 · Cited by 59 · see citing works
A population code for spatial representation in the zebrafish telencephalon
Yang, C., Mammen, L., Kim, B., Li, M., Robson, D. N., & Li, J. M. (2024) · Nature · doi:10.1038/s41586-024-07867-2 · Cited by 38 · see citing works
Evaluating Cognitive Maps and Planning in Large Language Models with CogEval
Momennejad, I., Hasanbeig, H., Frujeri, F. V., Sharma, H., Jojic, N., Palangi, H., Ness, R., & Larson, J. (2023) · Advances in Neural Information Processing Systems 36 · doi:10.52202/075280-3056 · Cited by 27 · see citing works
Emergence of Maps in the Memories of Blind Navigation Agents
Wijmans, E., Savva, M., Essa, I., Lee, S., Morcos, A. S., & Batra, D. (2023) · AI Matters · doi:10.1145/3609468.3609471 · Cited by 17 · see citing works
Cognitive Maps for a Non-Euclidean Environment: Path Integration and Spatial Memory on a Sphere
Kim, M., & Doeller, C. F. (2024) · Psychological Science · doi:10.1177/09567976241279291 · Cited by 9 · see citing works
Hope, S. F., Willgohs, K. R., Dittakul, S., & Plotnik, J. M. (2025) · Learning & Behavior · doi:10.3758/s13420-024-00655-y · Cited by 8 · see citing works
Does viewing a top-down map facilitate spatial learning from navigation in a virtual environment?
Ding, J., Chan, H. M., & Saunders, J. A. (2026) · Cognitive Research: Principles and Implications · doi:10.1186/s41235-026-00732-y
Does Spatial Cognition Emerge in Frontier Models?
Ramakrishnan, S. K., Wijmans, E., Kraehenbuehl, P., & Koltun, V. (2024) · arXiv · doi:10.48550/arxiv.2410.06468
- Authors
- O'Keefe, J., & Nadel, L.
- Affiliations
- University College London (GB)
- Dalhousie University (CA)
- Venue
- Behavioral and Brain Sciences
- Publisher
- Cambridge University Press (CUP)
- Published
- 1979-12
- Volume
- 2
- Issue
- 4
- Pages
- 520-533
- ISSN
- 0140-525X (ISSN-L)
- 1469-1825
- OpenAlex
- W2165260182
- Cited by
- 125
- References
- 6
- Citations by year
- 2026: 5 · 2025: 11 · 2024: 4 · 2023: 4 · 2022: 4 · 2021: 1 · 2020: 1 · 2019: 3 · 2018: 1 · 2017: 2 · 2016: 1 · 2015: 4 · 2014: 2 · 2013: 1 · 2012: 2
- FWCI
- 0.23
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioral and Brain Sciences (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Physical Sciences › Engineering › Automotive Engineering › Spatial Cognition and Navigation
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Keywords
- cognitive maps, hippocampus, spatial learning, spatial memory
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review