Classic Mazes
Used in a Cell paper

Morris Water Maze

SKU 3101-04
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Gold standard circular water maze for assessing spatial learning and memory in rodents through hippocampal-dependent navigation tasks.

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Size SKU 3101-04
Color SKU 3101-04
$1,790.00
Unit: Each
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Louise Corscadden, PhD, Director of Science

Louise Corscadden, PhD

Director of Science · ConductScience

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Used in a 2018 paper in the journal Cell

“Dissociable Structural and Functional Hippocampal Outputs via Distinct Subiculum Cell Classes”

From the methods
The water maze (tank: ∼1.2 m diameter, Maze Engineers, Cambridge, MA) was maintained at 24°C, with water made opaque through addition of non-toxic white tempera paint.

Maze Engineers, the maker named in the paper, is part of ConductScience.

See all 13 papers citing this product

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Mouse, Rat
SKU family
3101/3102/3103
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4 Ft (Mouse): Diameter 120 cm · Height 81 cm; 5ft (Intermediate): Diameter 155 cm · Height 89 cm; 6 Ft (Rat): Diameter 180 cm · Height 76 cm
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Classic Mazes
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Category: Classic Mazes

Score this test with ConductVision

ConductVision is our video-tracking software. Record your sessions on video, and it reports the measures listed below.

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Creator Insights

Richard G. M. MorrisDeveloped the Morris Water Maze (1981–1984)University of Edinburgh

About the Creator

Richard G. M. Morris is a British neuroscientist and Professor of Neuroscience at the University of Edinburgh, where much of his career has been spent studying how the brain forms and stores memories. A Fellow of the Royal Society, his research centers on the hippocampus, spatial learning, and the synaptic mechanisms — including NMDA-receptor-dependent long-term potentiation — that underlie memory formation and consolidation. He developed the water maze in the early 1980s to test whether animals could navigate to a hidden goal using distal spatial cues alone, and the task has since become one of the most widely used assays of hippocampus-dependent spatial memory in neuroscience.

To view Richard G. M. Morris’s publications, visit PubMed.

Are you Richard G. M. Morris? to review your photo and bio, and find out how to submit Creator Insights.

ConductScience celebrates method creators: researchers who, through rigorous and often ingenious experiments, develop the tools that reveal how the brain and body work. These are real scientific discoveries that become everyday instruments for the labs that follow.

Foundational papers
  1. Morris, R. G. M. (1981). Spatial localization does not require the presence of local cues. Learning and Motivation, 12(2), 239–260. doi:10.1016/0023-9690(81)90020-5
  2. Morris, R. G. M., Garrud, P., Rawlins, J. N. P., & O’Keefe, J. (1982). Place navigation impaired in rats with hippocampal lesions. Nature, 297(5868), 681–683. doi:10.1038/297681a0
  3. Morris, R. (1984). Developments of a water-maze procedure for studying spatial learning in the rat. Journal of Neuroscience Methods, 11(1), 47–60. doi:10.1016/0165-0270(84)90007-4

§ 1

Introduction

The Morris Water Maze is a hippocampal-dependent spatial learning task in which rodents learn the location of a hidden escape platform using distal room cues. Morris introduced the task as a way to separate place learning from simple cue approach behavior, and it became the reference assay for spatial memory because the platform can be removed during a probe trial to test memory without reinforcement. 1

The paradigm is widely used in Alzheimer disease, traumatic brain injury, stroke, aging, and pharmacology because acquisition curves, search strategy, and probe-trial bias can be measured in the same apparatus. 1 The visible-platform control is essential because motor impairment, visual impairment, thermoregulation, and stress reactivity can all masquerade as memory deficits. 2

A strong MWM methods section therefore needs pool size, platform, cue, and tracking details alongside enough protocol context to avoid swim-stress and motor-confound errors. 1

§ 2

Methods

2.1 Procedure

Hidden-platform acquisition followed by probe and visible-platform control trials.

Pre-test setup

  1. 1.Room cues: Place stable distal cues around the pool before habituation. Do not move cues between acquisition and probe sessions.
  2. 2.Water preparation: Fill the pool with opaque water at the protocol temperature used for all groups, typically 20 to 26 C depending on strain and ethics protocol.
  3. 3.Platform calibration: Set hidden platform 0.5 to 1 cm below the water surface. Confirm the platform cannot be seen from the release points.
  4. 4.Tracking calibration: Calibrate the overhead camera to the pool edge and define quadrant, annulus, wall, and platform zones before the first subject.

Trial sequence

  1. 1.Release subject: Release from pseudo-randomized compass positions facing the pool wall.
  2. 2.Acquire trial: Allow up to 60 seconds to find the hidden platform. If the animal fails, guide it to the platform and score maximum latency.1
  3. 3.Platform dwell: Leave the subject on the platform for 10 to 20 seconds to encode the location.
  4. 4.Inter-trial interval: Dry the animal, maintain temperature, and keep inter-trial intervals consistent within cohort.
  5. 5.Probe trial: Remove the platform and record a 60-second search trial after acquisition reaches criterion.

Critical methodological constraints

  • Motor and vision controls. Always include a visible-platform trial or control phase when genotype, injury, age, or treatment could affect swim speed or vision.3
  • Stress and hypothermia. Water temperature, trial spacing, and drying procedure must be fixed. A cognitive deficit claim is weak if body temperature or floating behavior differs by group.
  • Cue stability. Moving room cues between days converts the task into an uncontrolled reversal problem.
  • Strategy matters. Latency alone can improve through non-spatial chaining or thigmotaxis reduction. Report path efficiency and search strategy alongside latency.

2.2 Measurement & Analysis

Core MWM metrics ConductVision scores from swim trajectories.

Escape Latency

Acquisition curve

Time to reach the hidden platform. Interpretable only with swim speed and visible-platform controls.1

Path Length

Motor-normalized learning

Distance swum before platform discovery. Less sensitive than latency to swim-speed differences.

Target Quadrant Time

Probe memory

Percent of probe trial spent in the former platform quadrant after the platform is removed.2

Platform Crossings

Spatial precision

Number of crossings through the exact former platform location during the probe trial.

Thigmotaxis

Search strategy control

Time near the wall. Persistent wall-hugging can obscure spatial learning and should be reported.

+ Additional metrics: swim speed, heading error, cumulative search error, annulus crossings, quadrant entropy, floating time, and path efficiency.

2.3 target quadrant preference (analysis)

A simple probe-trial index: target quadrant time divided by total quadrant time.

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Full calculator with 95% CI ->
Target preference

40.0%

Formula: target quadrant time / (target quadrant time + other quadrant time) x 100. Chance performance is 25% in a four-quadrant probe. Interpret alongside platform crossings and path strategy. 1

§ 3

Results

3.1 Sample apparatus output

Representative acquisition and probe output from a hidden-platform study.

Table 1 · Per-animal Morris Water Maze scoring output

AnimalGroupLatency (s)Path (m)Target quadrant (s)Preference (%)
MWM-001Control214.82541.7%
MWM-002Control184.22745.0%
MWM-003Control245.02338.3%
MWM-004Impaired448.61626.7%
MWM-005Impaired519.31423.3%
MWM-006Impaired478.91525.0%

Synthetic example for illustration only. Interpret probe preference with platform crossings and visible-platform controls.

§ 4

Discussion

Limitations of the paradigm, methodological caveats, and current directions.

4.1 Common confounds

Variables that can shift Morris Water Maze results apart from the effect under study.

Swim speed

Latency increases when animals swim slowly. Report path length and swim speed before calling a latency change a memory deficit.3

Floating behavior

Floating and passive coping reduce apparent search. Track immobility separately from spatial navigation.

Visual acuity

Visual impairment can impair cue-based navigation. Visible-platform performance is the practical control.

Temperature

Cold water changes motivation and physiology. Keep temperature constant and monitor vulnerable strains or aged animals.

Non-spatial strategies

Chaining, circling, and wall-hugging can reduce latency without true place learning. Strategy labels help separate these cases.

4.2 Construct validity caveats

MWM is powerful because it couples acquisition with a probe trial, but it is also stressful and motor-loaded. 1 Studies involving injury, aging, frailty, or motor phenotypes should report visible-platform controls, swim speed, and path-based endpoints before interpreting latency as cognition. 2

4.3 Special considerations

When should I use Barnes Maze instead?

Use Barnes Maze when swimming stress, hypothermia, motor impairment, or repeated longitudinal testing would confound MWM interpretation. 1

Is escape latency enough?

No. Latency should be paired with path length, swim speed, thigmotaxis, and probe-trial measures because latency can improve through non-spatial strategies.

How many acquisition days are typical?

Many protocols use 4 to 6 acquisition days with several trials per day, then a probe trial after criterion or the final acquisition day. Match schedule to strain, age, and manipulation.

4.4 Current directions

Quarterly editorial review of emerging Morris Water Maze methodology. Q2 2026

Methods

Path strategy classification

Automated strategy labels are increasingly reported with latency to distinguish spatial search from chaining and thigmotaxis.

Emerging

Longitudinal disease models

AD, TBI, and stroke studies increasingly combine MWM with dry-land spatial tasks to separate memory from motor and stress effects.

Methods

Visible-platform normalization

Reviewers expect visible-platform controls when treatments plausibly affect motor function, vision, or motivation.

Emerging

Pose and thermal monitoring

Thermal management and posture-aware scoring are becoming standard for aged and injured cohorts.

§ 5

Background references

10 selected methods and validation studies of the Morris Water Maze, from any lab.

  1. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods. 1984;11(1):47-60. Find source
  2. Vorhees CV, Williams MT. Morris water maze: procedures for assessing spatial and related forms of learning and memory. Nat Protoc. 2006;1(2):848-858. Find source
  3. Vorhees CV, Williams MT. Assessing spatial learning and memory in rodents. ILAR J. 2014;55(2):310-332. Find source
  4. D'Hooge R, De Deyn PP. Applications of the Morris water maze in the study of learning and memory. Brain Res Brain Res Rev. 2001;36(1):60-90. Find source
  5. Barnes CA. Memory deficits associated with senescence: a neurophysiological and behavioral study in the rat. J Comp Physiol Psychol. 1979;93(1):74-104. Find source
  6. Garthe A, Kempermann G. An old test for new neurons: refining the Morris water maze to study adult hippocampal neurogenesis. Front Neurosci. 2013;7:63. Find source
  7. Whishaw IQ. A comparison of rats and mice in a swimming pool place task and matching-to-place task: some surprising differences. Physiol Behav. 1995;58(4):687-693. Find source
  8. Wolfer DP, Lipp HP. Dissecting the behaviour of transgenic mice: is it the mutation, the genetic background, or the environment? Exp Physiol. 2000;85(6):627-634. Find source
  9. Janus C. Search strategies used by APP transgenic mice during navigation in the Morris water maze. Learn Mem. 2004;11(3):337-346. Find source
  10. Hodges H. Maze procedures: the radial-arm and water maze compared. Brain Res Cogn Brain Res. 1996;3(3-4):167-181. Find source
Morris Water Maze
Morris Water Maze
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