The DOI matches its Crossref record; 290 of the 291 references it cites were found in a registry or an index.
Associations across time: The hippocampus as a temporary memory store
Abstract
All recent memory theories of hippocampal function have incorporated the idea that the hippocampus is required to process items only of some qualitatively specifiahle kind, and is not required to process items of some complementary set. In contrast, it is now proposed that the hippocampus is needed to process stimuli of all kinds, but only when there is a need to associate those stimuli with other events that are temporally discontiguous. In order to form or use temporally discontiguous associations, it is essential to maintain some memory of the first component until the second component has occurred. When the temporal gap to he spanned is small, and the number of items to be temporarily retained is low, a limited-capacity, short-term store is sufficient to allow associations to be formed. Such a store is presumed to operate in parallel with the hippocampus in normal animals. Hippocampal damage disrupts a much higher-capacity store that has a slower decay rate, and so leaves animals with only a very limited ability to form temporally discontiguous associations. Hippocampal damage, however, is not held to affect the long-term storage of associations of any kind, if they can be formed. Analyses of both new and existing data are presented to show that by classifying tasks in terms of the need to use a temporary memory store to retain temporally discontiguous information one can cut right across existing classifications as well as achieve a better fit to the data. The hippocampus thus seems best described as a high-capacity, intermediate-term memory store.
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“Thus, the mammalian hippocampus seems to be also essential to encode the time and order of events, to associate temporally separate stimuli, and to register non-spatial contextual information [216,217,218,219].”
From Spatial Cognition in Teleost Fish: Strategies and Mechanisms (2021) · cites this paper as [219]
Citations
Cites
Telling more than we can know: Verbal reports on mental processes.
Nisbett, R. E., & Wilson, T. D. (1977) · Psychological Review · doi:10.1037/0033-295x.84.3.231 · Cited by 11,317
Philosophical transactions of the Royal Society of London. B
Press, H. (1886) · Cited by 10,087
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
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
The hippocampus as a cognitive map
Passingham, R. E. (1979) · Neuroscience · doi:10.1016/0306-4522(79)90015-0 · Cited by 5,128
The Psychology of Learning and Motivation
(2021) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(21)x0002-3 · Cited by 5,082
Gray, J. A. (1982) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00013066 · Cited by 4,477
Marr, D. (1969) · The Journal of Physiology · doi:10.1113/jphysiol.1969.sp008820 · Cited by 3,253
The psychology of fear and stress
(1988) · Choice Reviews Online · doi:10.5860/choice.26-2399 · Cited by 3,133
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
Research works printed but not linked: 44
- Wycis, 1972, Psychosurgery
- Weiskrantz, 1975, The hippocampus, vol. 2. Neurophysiology and behavior
- Vanderwolf, 1975, The hippocampus, vol. 2. Neurophysiology and behavior
- Stephan, 1975, Handbuch der mikroskopischen Anatomic des Menschen, 4
- Squire, 1984, Memory Consolidation
- Sharp, 1983, Spontaneous synaptic enhancement in hippocampi of rates exposed to a spatially complex environment, Society for Neuroscience Abstracts, 9, 647
- 10.1037/0735-7044.98.2.211 · DOI
- Roberts, 1984, Animal cognition
- 10.1037/0735-7044.97.6.857 · DOI
- Rao, 1984, Retrograde spatial amnesia gradient following hippocampal LTE, Society for Neuroscience Abstracts, 10, 126
- Pavlov, 1928, Conditioned reflexes
- 10.1037/0735-7044.97.4.595 · DOI
- Maki, 1984, Effects of electroconvulsive shock upon proactively interfering spatial memories
- Jarrard, The hippocampus
- 10.1037/0735-7044.97.6.873 · DOI
- Hughey, 1982, The effects of hippocampal lesions in rats on the learning of a sequence of intra-maze stimuli
- Houk, 1980, Medical physiology, 1
- Honig, 1984, Animal cognition
- Gray, The hippocampus
- Gibbon, 1984, Annals of the New York Academy of Sciences: Timing and time perception, 423
- Geschwind, 1974, Plasticity and recovery of function in the central nervous system
- Farthing, 1973, Cognitive processes in animal behavior
- Dennett, 1978, Brainstorms
- Capaldi, 1967, The psychology of learning and motivation, 1
- Brookes S. (1981) Behavioural aspects of septo-hippocampal function. D. Phil. thesis, Oxford University. [taJNPR]
- Barnes, 1980, The psychobiology of aging: Problems and perspectives
- Baddeley, 1977, Human memory, basic processes
- Brown, 1984, Hippocampal single-unit activity during rats' performance of a visual recognition memory task, Journal of Physiology (London), 350, 74P
- Rawlins, 1982, Behavioral effects of hippocampectomy depend on inter-event intervals, Society for Neuroscience Abstracts, 8, 22
- Weisz, 1980, The hippocampus appears necessary for trace conditioning, Bulletin of the Psychonomic Society Abstracts, 194
- Milner, 1962, Physiologic de l'hippocampe
- Doinikow, 1908, Beitrag zur vergleichenden Histologie des Ammonshorns, Journal für Psychologie und Neurologie, 13, 166
- Gray, 1982, The neuropsychology of anxiety: An enquiry into the functions of the septo-hippocampal system
- Olton, 1984, Animal cognition
- McNaughton, 1979, Cooperativity in the generation of post-tetanic synaptic enhancement appears to require near simultaneity of afferent input, Society for Neuroscience Abstracts, 5, 631
- Barnes, 1983, Where is the cognitive map?, Society for Neuroscience Abstracts, 9, 649
- Gray, 1984, Animal cognition
- Mishkin, 1984, Neuropsychology of memory
- 10.1037/0735-7044.97.1.42 · DOI
- 10.1037/0735-7044.99.2.233 · DOI
- 10.1037/0735-7044.98.6.946 · DOI
- Brierley, 1977, Amnesia
- Cohen, 1984, Neuropsychology of memory
- Revusky, 1971, Animal memory
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Coupled nonlinear maps as models of perceptual pattern and memory trace dynamics
van Leeuwen, C., & Raffone, A. (2001) · IRIS Research product catalog (Sapienza University of Rome) · Cited by 17
Effects of medial septal lesions on an operant delayed go/no-go discrimination in rats
Numan, R., & Klis, D. (1992) · Brain Research Bulletin · doi:10.1016/0361-9230(92)90133-i · Cited by 17
Extending Models of Hippocampal Function in Animal Conditioning to Human Amnesia
Gluck, M. A., Ermita, B. R., Oliver, L. M., & Myers, C. E. (1997) · Memory · doi:10.1080/741941141 · Cited by 17
Evidence for disrupted NMDA receptor function in tissue plasminogen activator knockout mice
Horwood, J. M., Ripley, T. L., & Stephens, D. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(03)00248-1 · Cited by 17
Toumane, A., & Durkin, T. (1993) · Behavioral and Neural Biology · doi:10.1016/0163-1047(93)90243-b · Cited by 17
The NMDA antagonist MK-801 affects nonspatial learning in preweanling rats.
Highfield, D. A., Nixon, K., & Amsel, A. (1996) · Behavioral Neuroscience · doi:10.1037//0735-7044.110.2.300 · Cited by 17
Hippocampus, space, and relations
Nadel, L. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035597 · Cited by 17
Appetitively motivated instrumental learning in SynGAP heterozygous knockout mice.
Muhia, M., Feldon, J., Knuesel, I., & Yee, B. K. (2009) · Behavioral Neuroscience · doi:10.1037/a0017118 · Cited by 18
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Hamilton, V. (1988) · Springer eBooks · doi:10.1007/978-94-009-2792-6_17 · Cited by 16
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Honey, R. C. (2000) · The Quarterly Journal of Experimental Psychology Section B · doi:10.1080/027249900392977 · Cited by 15
Delay-dependent impairment of reversal learning in rats treated with trimethyltin
Bushnell, P. J. (1990) · Behavioral and Neural Biology · doi:10.1016/0163-1047(90)91261-9 · Cited by 15
Nelson, A., Sowinski, P., & Hodges, H. (1997) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1996.3758 · Cited by 15
Hippocampal muscarinic supersensitivity after AF64A medial septal lesion excludes M1 receptors
Dawson, V. L., & Wamsley, J. K. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90076-c · Cited by 15
Temporal and spatial contiguity are necessary for competition between events.
Herrera, E., Alcalá, J. A., Tazumi, T., Buckley, M. G., Prados, J., & Urcelay, G. P. (2022) · Journal of Experimental Psychology Learning Memory and Cognition · doi:10.1037/xlm0001108 · Cited by 23
Myhrer, T., & Johannesen, T. S. (1995) · Brain Research Bulletin · doi:10.1016/0361-9230(94)00237-u · Cited by 14
Tomie, J.-A., & Whishaw, I. Q. (1990) · Physiology & Behavior · doi:10.1016/0031-9384(90)90305-n · Cited by 14
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Warner, T. A., Stafford, N. P., Rompala, G. R., Hoogenstyn, A. J. V., Elgert, E., & Drugan, R. C. (2013) · Pharmacology Biochemistry and Behavior · doi:10.1016/j.pbb.2013.09.014 · Cited by 15
Rachlin, H. C. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040589 · Cited by 13
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Olton, D. S. (1991) · Elsevier eBooks · doi:10.1016/b978-0-12-474993-1.50016-x · Cited by 12
Hippocampal lesions and temporally chained conditioned stimuli in a conditioned suppression paradigm
Leaton, R. N., & Borszcz, G. S. (1990) · Psychobiology · doi:10.3758/bf03327219 · Cited by 12
Myhrer, T., & Andersen, J. M. (2001) · European Journal of Pharmacology · doi:10.1016/s0014-2999(01)01348-6 · Cited by 12
Medial septal lesions impair performance on a preoperatively acquired delayed alternation task
Numan, R. (1991) · Brain Research Bulletin · doi:10.1016/0361-9230(91)90023-d · Cited by 12
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Schmajuk, N. A., & DiCarlo, J. J. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065353 · Cited by 12
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Olton, D. S. (1986) · Elsevier eBooks · doi:10.1016/b978-0-12-474991-7.50016-8 · Cited by 12
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Clarke, R. P. M. (2000) · Medical Hypotheses · doi:10.1054/mehy.2000.1082 · Cited by 9
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Roitblat, H. L., Harley, H. E., & Helweg, D. A. (1989) · Psychobiology · doi:10.3758/bf03337800 · Cited by 10
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Remembering spatial cognition as a hippocampal functional component
Bingman, V. P. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x0003541x · Cited by 8
Olton, D. S. (1989) · The Psychology of learning and motivation/The psychology of learning and motivation · doi:10.1016/s0079-7421(08)60533-2 · Cited by 8
Does it still make sense to develop a declarative memory theory of hippocampal function?
Rawlins, J. N. P., Deacon, R. M. J., Yee, B. K., & Cassaday, H. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035615 · Cited by 7
Self-citationDurkin, T., Cazala, P., & Garcia, R. (2000) · Springer eBooks · doi:10.1007/978-1-4612-1302-4_7 · Cited by 7
Effects of Unilateral Entorhinal Cortex Lesion on Retention of Water Maze Performance
Glasier, M. M., Janis, L. S., Roof, R. L., & Stein, D. G. (1999) · Neurobiology of Learning and Memory · doi:10.1006/nlme.1998.3832 · Cited by 7
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Carlsson, A., & Carlsson, M. L. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065067 · Cited by 7
Rawlins, J. N. P. (1987) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00056764 · Cited by 7
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Myhrer, T., & Iversen, E. G. (1990) · Brain Research Bulletin · doi:10.1016/0361-9230(90)90074-a · Cited by 7
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Kinsbourne, M. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040528 · Cited by 7
Psychoarithmetic or pick your own?
Gray, J. A., Sinden, J. D., & Hodges, H. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035470 · Cited by 7
Dennett, D. C. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040413 · Cited by 7
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Rosenzweig, M. R. (1998) · Elsevier eBooks · doi:10.1016/b978-012475655-7/50002-2 · Cited by 7
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Differential Effects of 8-OH-DPAT on Two Forms of Appetitive Pavlovian Conditioning in the Rat.
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Spatial Learning and Its Neural Basis in Fish ☆
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Higgs, S., Bannerman, D. M., & Rawlins, J. N. P. (2001) · Behavioral Neuroscience · doi:10.1037//0735-7044.115.6.1193 · Cited by 6
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Lattal, K. A., & Abreu‐Rodrigues, J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00033719 · Cited by 6
Smith, J. D. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040632 · Cited by 6
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Revonsuo, A. (1995) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00040607 · Cited by 6
Language Learning and the Brain: A Comprehensive Survey of Recent Conclusions
Munsell, P., Rauen, M. G., & Kinjo, M. (1988) · Language Learning · doi:10.1111/j.1467-1770.1988.tb00412.x · Cited by 6
Selective impairment of fornix‐transected rats on a new nonspatial, odor‐guided task
Hudon, C., Doré, F. Y., & Goulet, S.-M. (2002) · Hippocampus · doi:10.1002/hipo.10061 · Cited by 6
Hippocampus and memory for time
Kesner, R. P. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035548 · Cited by 6
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Gray, J. A., & McNaughton, N. (2003) · Oxford University Press eBooks · doi:10.1093/acprof:oso/9780198522713.003.0005 · Cited by 6
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Dawson, M. E., & Hazlett, E. A. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065110 · Cited by 6
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Eichenbaum, H., Otto, T., & Cohen, N. J. (1994) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00035688 · Cited by 6
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Lubow, R. E. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065237 · Cited by 6
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Weiner, I. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065407 · Cited by 6
Maki, W. S. (1986) · PubMed · Cited by 6
Olton, D. S. (1987) · Springer eBooks · doi:10.1007/978-94-009-3533-4_2 · Cited by 6
Recall of sequences based on the position of the first cue stimulus in rats
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Vorobyov, N. A., & Brown, M. W. (2008) · European Journal of Neuroscience · doi:10.1111/j.1460-9568.2008.06257.x · Cited by 6
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Consciousness does not seem to be linked to a single neural mechanism
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Hunting for consciousness in the brain: What is (the name of) the game?
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Excitatory amino acids, NMDA and sigma receptors: A role in schizophrenia?
Jansen, K. L. R., & Faull, R. L. M. (1991) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00065225 · Cited by 5
Metadata
- Authors
- Rawlins, J. N. P.
- Affiliations
- University of Oxford (GB)
- Corresponding author
- Rawlins, J. N. P.
- Venue
- Behavioral and Brain Sciences
- Publisher
- Cambridge University Press (CUP)
- Published
- 1985-09
- Volume
- 8
- Issue
- 3
- Pages
- 479-497
- ISSN
- 0140-525X (ISSN-L)
- 1469-1825
- OpenAlex
- W1973789361
- Cited by
- 561
- References
- 291
- Citations by year
- 2026: 1 · 2025: 3 · 2024: 3 · 2023: 1 · 2022: 1 · 2021: 4 · 2020: 1 · 2019: 2 · 2018: 4 · 2017: 6 · 2016: 5 · 2015: 5 · 2014: 6 · 2013: 7 · 2012: 6
- FWCI
- 16.74
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Behavioral and Brain Sciences (publishedVersion)
- Topics
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
- Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
- Social Sciences › Psychology › Experimental and Cognitive Psychology › Cognitive Functions and Memory
- Keywords
- hippocampus, temporal association, short-term memory, intermediate-term memory, hippocampal lesions, memory decay, long-term memory, memory theory, task classification
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 ›
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