Classic Mazes

Morris Water Maze

$1,490.00 - $1,990.00

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

Size: Intermediate
Color: White
$1,690.00
Key Specifications
Automation Levelsemi-automated
SpeciesMouse, Rat
Dimensions1.3 m diameter x 1.3 m diameter x 0.6 m
SKU:3101/3102/3103
Category:Classic Mazes
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Choose your configuration

Validated Morris Water Maze configurations

Pick the apparatus configuration that matches the cohort, species, and protocol. Species-specific adaptations should be interpreted within their own validation literature.

This productRat standard

120 cm Morris Water Maze

120 cm pool diameter, opaque water, adjustable hidden platform

Standard rat configuration for spatial acquisition, probe, reversal, and visible platform control trials.

$1,490

BuyableMouse standard

90 cm Mouse Water Maze

90 cm pool diameter, low-volume water handling, scaled platform

Mouse-sized arena for transgenic and pharmacological spatial-learning studies.

$1,490

SpecialtyHigh-throughput

150 cm Large-Cohort MWM

150 cm pool diameter, larger field of view, modular platform positions

Larger arena for adult rats, strategy analysis, and protocols requiring wider cue separation.

$1,990

§ 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 page must therefore treat the apparatus as both a commercial product and a methods reference: buyers need pool size, platform, cue, and tracking options, while researchers need enough protocol detail 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 cuesPlace stable distal cues around the pool before habituation. Do not move cues between acquisition and probe sessions.
  2. 2.Water preparationFill 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 calibrationSet hidden platform 0.5 to 1 cm below the water surface. Confirm the platform cannot be seen from the release points.
  4. 4.Tracking calibrationCalibrate the overhead camera to the pool edge and define quadrant, annulus, wall, and platform zones before the first subject.

Trial sequence

  1. 1.Release subjectRelease from pseudo-randomized compass positions facing the pool wall.
  2. 2.Acquire trialAllow 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 dwellLeave the subject on the platform for 10 to 20 seconds to encode the location.
  4. 4.Inter-trial intervalDry the animal, maintain temperature, and keep inter-trial intervals consistent within cohort.
  5. 5.Probe trialRemove 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.

Inline calculator

Type the times your tracker recorded.

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

Aggregate publication data, sample apparatus output, and recent findings from the live PubMed feed.

3.1 Publication trends

PubMed volume and co-occurring behavioral methods for spatial-learning studies.

Figure 1 · EPM publications by year (PubMed)

The paradigm has been dominant for 40 years and is still growing.

Live · Weekly

2000201020202026 YTD: 450 papers

Total in PubMed since 1985: 16,237+ papers. Updated 2026-05-04.

Figure 2 · Methods co-occurring with EPM (last 12 months)

Other paradigms most often run alongside EPM in the same paper.

Live

3.2 Sample apparatus output

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

Table 1 · Per-animal EPM scoring output

Download sample CSV →
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.

3.3 Recent findings (live PubMed feed)

  • May 2026PMID: 41865827

    Therapeutic efficacy of engineered exosomes in Alzheimer's disease: A systematic review and meta-analysis of preclinical animal models.

    Li A, Peng W, Wu B, et al.. Neuroscience. 2026 May 25.

    Engineered exosomes are modified extracellular vesicles designed to enhance targeting and cargo delivery, and they have been proposed as a therapeutic strategy for Alzheimer's disease.

  • May 2026PMID: 41933605

    Increased NMDA receptor GluN2A-type ionotropic signaling is sufficient to improve spatial memory in immature mice.

    Boakye-Agyei AS, Rodrigues-Henry DDM, Gonzalez DA, et al.. Neurosci Lett. 2026 May 15.

    Spatial learning and memory are reliant on activation of N-methyl-D-aspartate receptors (NMDARs) at excitatory synapses in the hippocampus. NMDARs at immature synapses contain mostly GluN2B subunits while at mature synapses, more NMDARs contain GluN2A subunits.

  • May 2026PMID: 41865457

    Tetrahydrocoptisine alleviates postoperative delirium with sleep disturbances by modulating the TH/NLRP3 Inflammasome pathway.

    Liu X, Yang C, Wang X, et al.. Int Immunopharmacol. 2026 May 15.

    Postoperative delirium (POD) accompanied by sleep disturbances (SD) represents a significant concern in perioperative neurocognitive health.

  • May 2026PMID: 41687942

    Polygonatum Sibiricum polysaccharide ameliorates Alzheimer's disease by alleviating cuproptosis and activating the PI3K/AKT signaling pathway.

    Wang S, Guo Y, Wang S, et al.. J Ethnopharmacol. 2026 May 10.

    Defined by the selective loss of central nervous system neurons, a progressive neurodegenerative disorder is what Alzheimer's disease (AD) constitutes. It is recognized as the leading cause of dementia globally.

View all 16237 matching papers on PubMed →

§ 4

Discussion

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

4.1 Common confounds

Variables that shift Morris Water Maze results independent of anxiety state.

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

Methodological

Path strategy classification

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

Rising

Longitudinal disease models

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

Methodological

Visible-platform normalization

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

Rising

Pose and thermal monitoring

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

§ 5

References

6 curated Morris Water Maze methods and validation papers. Schema-marked as ScholarlyArticle ItemList.

  1. Morris R. Developments of a water-maze procedure for studying spatial learning in the rat. J Neurosci Methods. 1984;11(1):47-60.
  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.
  3. Vorhees CV, Williams MT. Assessing spatial learning and memory in rodents. ILAR J. 2014;55(2):310-332.
  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.
  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.
  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.
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