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

Gold standard circular water maze for assessing spatial learning and memory in rodents through hippocampal-dependent navigation tasks.
| Automation Level | semi-automated |
| Species | Mouse, Rat |
| Dimensions | 1.3 m diameter x 1.3 m diameter x 0.6 m |
The Morris Water Maze is the gold standard behavioral apparatus for assessing spatial learning and memory in rodents. Originally developed by Richard Morris in 1984, this paradigm exploits the natural aversion of rodents to water and their innate swimming ability to evaluate hippocampal-dependent spatial navigation. The test involves placing animals in a circular pool filled with opaque water containing a hidden platform that provides escape from the water.
This apparatus features a 1.3-meter diameter circular pool with 0.6-meter walls, accommodating both mice and rats. The water level is maintained at 0.4 meters above the base, with the invisible platform positioned 1 cm below the surface at 0.39 meters height. The platform's silvery-white color ensures it remains concealed beneath the opaque water, while a visible black platform at 0.4 meters height serves for control trials and initial training phases.
The Morris Water Maze operates on the principle that rodents possess an innate aversion to water and will actively seek an escape platform. During acquisition trials, animals are placed at various starting positions around the pool perimeter and must navigate to locate the hidden platform using distal visual cues positioned around the testing room. The opaque water prevents animals from seeing the platform directly, forcing reliance on spatial memory and cognitive mapping rather than local visual or olfactory cues.
The hippocampus constructs a cognitive map of the spatial environment through integration of visual landmarks, allowing animals to develop allocentric spatial representations. Performance is measured through latency to platform, path length, swimming speed, and search strategies. Probe trials, conducted with the platform removed, assess memory consolidation by measuring time spent in the target quadrant where the platform was previously located.
Multiple task variants can be implemented using the same apparatus, including reference memory tasks (fixed platform location), working memory protocols (changing platform positions), and reversal learning paradigms. The silvery-white invisible platform and black visible platform allow researchers to alternate between spatial memory testing and control conditions within the same experimental session.
| Feature | This Product | Typical Alternative | Advantage |
|---|---|---|---|
| Pool Diameter | 1.3 meters | Entry-level models often range from 1.0-1.2 meters | Larger diameter provides more spatial area for complex navigation strategies and reduces wall-hugging behavior. |
| Platform System | Dual platforms (visible black, invisible silvery-white) | Basic models may include only one platform type | Enables within-session comparison of spatial versus sensorimotor performance without apparatus changes. |
| Wall Height | 0.6 meters | Standard models typically offer 0.4-0.5 meter walls | Higher walls prevent escape attempts while providing better overhead tracking visibility. |
| Species Compatibility | Optimized for both mouse and rat testing | Many models are species-specific | Single apparatus accommodates diverse research programs without requiring separate equipment purchases. |
| Configuration Flexibility | Compatible with T-Maze, RAM, Y-Maze, Plus Maze variants | Standard models are limited to basic circular configuration | Multiple paradigms possible with same base apparatus, expanding experimental capabilities. |
| Customization Options | Available upon request | Fixed configurations with limited modification options | Accommodates specific research requirements and novel experimental protocols. |
This Morris Water Maze provides comprehensive spatial learning assessment capabilities through its dual platform system, species-flexible design, and configuration versatility. The 1.3-meter diameter and 0.6-meter walls offer optimal dimensions for robust behavioral phenotyping across multiple experimental paradigms.
Verify platform height daily using a ruler to ensure the invisible platform remains exactly 1 cm below water surface.
Why: Platform depth consistency is critical for standardized escape latencies and motivation levels.
Clean pool walls weekly with mild detergent to remove biofilm buildup that could provide tactile navigation cues.
Why: Wall cleanliness maintains reliance on distal visual cues rather than proximal tactile information.
Randomize starting positions across trials while maintaining equal representation of all quadrant entry points.
Why: Balanced start positions prevent development of response strategies that bypass spatial memory formation.
Record ambient room temperature and lighting conditions with each session to identify environmental variables affecting performance.
Why: Environmental consistency ensures that performance changes reflect experimental manipulations rather than testing conditions.
If animals show excessive floating behavior, reduce trial duration and increase inter-trial intervals to maintain motivation.
Why: Floating indicates learned helplessness that compromises spatial learning assessment.
Monitor animals continuously during trials and have towels readily available for immediate drying after platform location.
Why: Rapid drying prevents hypothermia and reduces stress that could influence subsequent trial performance.
Conduct probe trials at consistent time intervals after acquisition to standardize memory consolidation assessment.
Why: Timing consistency enables comparison of memory strength across different experimental groups.
Replace water opacity agents when platform becomes visible from any angle to maintain spatial memory requirements.
Why: Platform visibility compromises the cognitive demands of the task and invalidates spatial memory assessment.
ConductScience provides a one-year manufacturer warranty covering materials and workmanship defects, with technical support for setup and protocol optimization.
Background reading relevant to this product:
What is the Morris Water Maze?
The Morris Water Maze is a behavioral apparatus used to assess spatial learning and memory in rodents. Animals navigate a circular pool of opaque water to locate a hidden submerged platform, relying on external visual cues for orientation.
How does the Morris Water Maze work?
Rodents are placed in a water-filled circular pool where they must swim to find a hidden platform below the surface. Over repeated trials, researchers measure escape latency, path length, and swim patterns to quantify spatial memory acquisition and recall.
What research applications use the Morris Water Maze?
The Morris Water Maze is widely used in Alzheimer's disease research, drug screening for cognitive enhancers, and studies of hippocampal-dependent spatial memory. It is also applied in neurotoxicology and traumatic brain injury models.
Enhance your setup with compatible accessories
Use this apparatus with
Automate path length, quadrant occupancy, platform crossings, and probe trial heatmaps from overhead video.
ConductVision MWM →Acquisition, visible platform, probe, reversal, and working-memory schedules with metric definitions.
ConductMaze MWM Protocol →Free tool for escape latency, path efficiency, target quadrant preference, and probe trial summaries.
MWM Analyzer →Choose your configuration
Pick the apparatus configuration that matches the cohort, species, and protocol. Species-specific adaptations should be interpreted within their own validation literature.
120 cm pool diameter, opaque water, adjustable hidden platform
Standard rat configuration for spatial acquisition, probe, reversal, and visible platform control trials.
$1,490
90 cm pool diameter, low-volume water handling, scaled platform
Mouse-sized arena for transgenic and pharmacological spatial-learning studies.
$1,490
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
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
Hidden-platform acquisition followed by probe and visible-platform control trials.
Critical methodological constraints
Core MWM metrics ConductVision scores from swim trajectories.
Escape Latency
Acquisition curve
Path Length
Motor-normalized learning
Target Quadrant Time
Probe memory
Platform Crossings
Spatial precision
Thigmotaxis
Search strategy control
+ Additional metrics: swim speed, heading error, cumulative search error, annulus crossings, quadrant entropy, floating time, and path efficiency.
A simple probe-trial index: target quadrant time divided by total quadrant time.
§ 3
Aggregate publication data, sample apparatus output, and recent findings from the live PubMed feed.
PubMed volume and co-occurring behavioral methods for spatial-learning studies.
Representative acquisition and probe output from a hidden-platform study.
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.
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.
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.
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.
§ 4
Limitations of the paradigm, methodological caveats, and current directions.
Variables that shift Morris Water Maze results independent of anxiety state.
Latency increases when animals swim slowly. Report path length and swim speed before calling a latency change a memory deficit.3
Floating and passive coping reduce apparent search. Track immobility separately from spatial navigation.
Visual impairment can impair cue-based navigation. Visible-platform performance is the practical control.
Cold water changes motivation and physiology. Keep temperature constant and monitor vulnerable strains or aged animals.
Chaining, circling, and wall-hugging can reduce latency without true place learning. Strategy labels help separate these cases.
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
Use Barnes Maze when swimming stress, hypothermia, motor impairment, or repeated longitudinal testing would confound MWM interpretation. 1
No. Latency should be paired with path length, swim speed, thigmotaxis, and probe-trial measures because latency can improve through non-spatial strategies.
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.
Quarterly editorial review of emerging Morris Water Maze methodology. Q2 2026
Automated strategy labels are increasingly reported with latency to distinguish spatial search from chaining and thigmotaxis.
AD, TBI, and stroke studies increasingly combine MWM with dry-land spatial tasks to separate memory from motor and stress effects.
Reviewers expect visible-platform controls when treatments plausibly affect motor function, vision, or motivation.
Thermal management and posture-aware scoring are becoming standard for aged and injured cohorts.
§ 5
6 curated Morris Water Maze methods and validation papers. Schema-marked as ScholarlyArticle ItemList.