Spatial localization does not require the presence of local cues

Morris, Richard G.M.

doi:10.1016/0023-9690(81)90020-5

Cited by 2,699Memory and Neural MechanismsSpatial Cognition and NavigationMemory Processes and Influences

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Spatial localization does not require the presence of local cues

Morris, Richard G.M.·1981·Learning and Motivation

DOI 10.1016/0023-9690(81)90020-5

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In mouse behavioral studies, testing paradigms for learning and memory have been widely accepted.
“In mouse behavioral studies, testing paradigms for learning and memory have been widely accepted (Crawley, 2008; Crawley and Paylor, 1997; Morris, 1981).”
From Modeling Autism by SHANK Gene Mutations in Mice (2013) · cites this paper as Morris, 1981

Untitled work
(1978) · UA Campus Repository (The University of Arizona) · Cited by 8,010
The Psychology of Animal Learning
Hill, W. F., & Mackintosh, N. J. (1976) · The American Journal of Psychology · doi:10.2307/1421765 · Cited by 2,397
The Hippocampus as a Cognitive Map
Ranck, J. B. (1979) · American Journal of Psychiatry · doi:10.1176/ajp.136.10.1353 · Cited by 2,373
The psychology of animal learning
Lea, S. E. G. (1975) · Animal Behaviour · doi:10.1016/0003-3472(75)90150-5 · Cited by 2,067
Hippocampus, space, and memory
Olton, D. S., Becker, J. T., & Handelmann, G. E. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00062713 · Cited by 2,018
Remembrance of places passed: Spatial memory in rats.
Olton, D. S., & Samuelson, R. J. (1976) · Journal of Experimental Psychology Animal Behavior Processes · doi:10.1037/0097-7403.2.2.97 · Cited by 1,993
Two-process learning theory: Relationships between Pavlovian conditioning and instrumental learning.
Rescorla, R. A., & Solomon, R. L. (1967) · Psychological Review · doi:10.1037/h0024475 · Cited by 1,487
Some quantitative properties of anxiety.
Estes, W. K., & Skinner, B. F. (1941) · Journal of Experimental Psychology · doi:10.1037/h0062283 · Cited by 1,350
Mechanisms of Animal Discrimination Learning
Bitterman, M. E., Sutherland, N., & Mackintosh, N. J. (1972) · The American Journal of Psychology · doi:10.2307/1420674 · Cited by 954
Orientation of Animals
(1940) · BMJ · doi:10.1136/bmj.2.4169.744-b · Cited by 650
Discrimination of cues in mazes: A resolution of the "place-vs.-response" question.
Restle, F. (1957) · Psychological Review · doi:10.1037/h0040678 · Cited by 390
Context and conditioning: A place for space
Nadel, L., & Willner, J. (1980) · Physiological Psychology · doi:10.3758/bf03332853 · Cited by 379
Fornix lesions selectively abolish place learning in the rat
O'Keefe, J. M., Nadel, L., Keightley, S. J., & Kill, D. (1975) · Experimental Neurology · doi:10.1016/0014-4886(75)90230-7 · Cited by 337
Systematic foraging by a nectar-feeding bird, the amakihi (Loxops virens).
Kamil, A. C. (1978) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077479 · Cited by 295
Hormonal Effects on Ontogeny of Swimming Ability in the Rat: Assessment of Central Nervous System Development
Schapiro, S., Salas, M., & Vukovich, K. R. (1970) · Science · doi:10.1126/science.168.3927.147 · Cited by 234
Experimental Study of the Mental Processes of the Rat. II
Small, W. S. (1901) · The American Journal of Psychology · doi:10.2307/1412534 · Cited by 230
Spatial memory in the rat on a hierarchical maze
Roberts, W. A. (1979) · Learning and Motivation · doi:10.1016/0023-9690(79)90040-7 · Cited by 144
Information processing in space-time by the hippocampus
Moore, J. W. (1979) · Physiological Psychology · doi:10.3758/bf03326630 · Cited by 123
Analysis of behavioural change
Piercy, M. (1970) · Neuropsychologia · doi:10.1016/0028-3932(70)90015-1 · Cited by 114
A Study in Behaviour
Bentley, E. W., & Barnett, S. A. (1963) · Journal of Animal Ecology · doi:10.2307/2612 · Cited by 106
Role of the caudate nucleus in spatial orientation of rats.
Potegal, M. (1969) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0028168 · Cited by 100
Memory for lists of spatial events in the rat
Roberts, W. A., & Smythe, W. E. (1979) · Learning and Motivation · doi:10.1016/0023-9690(79)90036-5 · Cited by 78
Visual sampling after lesions of the superior colliculus in rats.
Milner, A. D., Goodale, M. A., & Morton, M. C. (1979) · Journal of Comparative and Physiological Psychology · doi:10.1037/h0077638 · Cited by 68
The Hippocampus as a Cognitive Map
Routtenberg, A., O'Keefe, J. M., & Nadel, L. (1980) · The American Journal of Psychology · doi:10.2307/1422119 · Cited by 65
Homing and related activities of birds
Watson, J. B., & Lashley, K. S. (1915) · Carnegie Institution of Washington eBooks · doi:10.5962/bhl.title.14554 · Cited by 52
Inner and outer space: the neuroanatomical bases of spatially organized behaviors
Olton, D. S. (1979) · Behavioral and Brain Sciences · doi:10.1017/s0140525x00064153 · Cited by 41
Papers from the department of marine biology of the Carnegie Institution of Washington. Vol. VII, Homing and related activities of birds. The Acquisition of skill in archery
Watson, J. B. (1915) · Cited by 14

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Are the Dorsal and Ventral Hippocampus Functionally Distinct Structures?
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Goldman-Rakic, P. S. (1995) · Neuron · doi:10.1016/0896-6273(95)90304-6 · Cited by 2,663
The human hippocampus and spatial and episodic memory
Burgess, N., Maguire, E. A., & O'Keefe, J. (2002) · Neuron · doi:10.1016/s0896-6273(02)00830-9 · Cited by 2,401
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Muller, R., & Kubie, J. (1987) · The Journal of Neuroscience · doi:10.1523/jneurosci.07-07-01951.1987 · Cited by 1,581
CREB AND MEMORY
Silva, A. J., Kogan, J. H., Frankland, P. W., & Kida, S. (1998) · Annual Review of Neuroscience · doi:10.1146/annurev.neuro.21.1.127 · Cited by 1,462
The value of spontaneous alternation behavior (SAB) as a test of retention in pharmacological investigations of memory
Hughes, R. N. (2004) · Neuroscience & Biobehavioral Reviews · doi:10.1016/j.neubiorev.2004.06.006 · Cited by 641
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Nakazawa, K., McHugh, T. J., Wilson, M. A., & Tonegawa, S. (2004) · Nature Reviews Neuroscience · doi:10.1038/nrn1385 · Cited by 619
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Bannerman, D. M., Grubb, M., Deacon, R. M. J., Yee, B. K., Feldon, J., & Rawlins, J. N. P. (2003) · Behavioural Brain Research · doi:10.1016/s0166-4328(02)00268-1 · Cited by 530
Spatial memory deficits in patients with lesions to the right hippocampus and to the right parahippocampal cortex
Bohbot, V. D., Kalina, M., Stepankova, K., Spackova, N., Petrides, M., & Nadel, L. (1998) · Neuropsychologia · doi:10.1016/s0028-3932(97)00161-9 · Cited by 516
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Social interaction and sensorimotor gating abnormalities in mice lacking Dvl1
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Spaced training induces normal long-term memory in CREB mutant mice
Kogan, J. H., Frankland, P. W., Blendy, J. A., Coblentz, J., Marowitz, Z., Schütz, G., & Silva, A. J. (1997) · Current Biology · doi:10.1016/s0960-9822(06)00022-4 · Cited by 350
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Self-citation
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Owen, E. H., Logue, S. F., Rasmussen, D. L., & Wehner, J. M. (1997) · Neuroscience · doi:10.1016/s0306-4522(97)00165-6 · Cited by 347
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Selcher, J. C., Atkins, C. M., Trzaskos, J. M., Paylor, R., & Sweatt, J. D. (1999) · Learning & Memory · doi:10.1101/lm.6.5.478 · Cited by 341
Bayesian integration of spatial information.
Cheng, K., Shettleworth, S. J., Huttenlocher, J., & Rieser, J. J. (2007) · Psychological Bulletin · doi:10.1037/0033-2909.133.4.625 · Cited by 326
Differential Effects of Ethanol on Memory in Adolescent and Adult Rats
Markwiese, B. J., Acheson, S. K., Levin, E. D., Wilson, W. A., & Swartzwelder, H. S. (1998) · Alcoholism: Clinical and Experimental Research · doi:10.1111/j.1530-0277.1998.tb03668.x · Cited by 320
Fragile X mouse: strain effects of knockout phenotype and evidence suggesting deficient amygdala function
Paradee, W., Melikian, H. E., Rasmussen, D. L., Kenneson, A., Conn, P. J., & Warren, S. T. (1999) · Neuroscience · doi:10.1016/s0306-4522(99)00285-7 · Cited by 305
Double dissociation of function within the hippocampus: Spatial memory and hyponeophagia.
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Authors: Morris, R. G. M.
Affiliations: University of St Andrews (GB)
Corresponding author: Morris, Richard G.M.
ORCID: Morris, Richard G.M.
Venue: Learning and Motivation
Publisher: Elsevier BV
Published: 1981-05
Volume: 12
Issue: 2
Pages: 239-260
ISSN: 0023-9690 (ISSN-L)
DOI: 10.1016/0023-9690(81)90020-5
OpenAlex: W2145107163
Cited by: 2,699
References: 27
Citations by year: 2026: 31 · 2025: 48 · 2024: 66 · 2023: 60 · 2022: 73 · 2021: 77 · 2020: 79 · 2019: 60 · 2018: 69 · 2017: 70 · 2016: 60 · 2015: 87 · 2014: 83 · 2013: 89 · 2012: 59
FWCI: 14.00
Type: journal article
Language: en
Open access: closed
Licence: www.elsevier.com/tdm/userlicense/1.0/ (tdm)
Locations: Learning and Motivation (publishedVersion)
Topics: Life Sciences › Neuroscience › Cognitive Neuroscience › Memory and Neural Mechanisms
Social Sciences › Psychology › Experimental and Cognitive Psychology › Spatial Cognition and Navigation
Life Sciences › Neuroscience › Cognitive Neuroscience › Memory Processes and Influences
Keywords: spatial localization, spatial memory, rats, escape learning, water maze, platform location, transfer of learning, operant conditioning, classical conditioning

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