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How does the ermine see?

The ermine (Mustela erminea) is a mammal in the order Carnivora. Its eyes belong to the vision type Night-hunting cat.

Measured in this species: sharpness and night vision. Measured colour or sharpness: a measured receptor set or acuity in this species; other dials come from relatives or group defaults. Every value below carries its evidence level and sources; nothing is typed by hand.

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What stands out

The six dials

Evidence levels: how the tiers work. "Measured" means a value measured in this species; "Estimated" values come from a close relative or an eye-size formula.

Vision values for the ermine (Mustela erminea), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
2 receptor classes: 430 nm (VS/SWS (violet)), 558 nm (LWS (long))
receptor set of nearest measured relative Mustela putorius (same genus Mustela)
Estimated[1][2]
SharpnessAcuity
1.55 cycles per degree
median of 1 behavioural rows (method priority rule)
Measured[3]
Field of viewBinocular overlap
74.5°
median of 2 relatives in genus Mustela: Mustela putorius, Mustela nivalis
Estimated[4][5]
Total field of view
250°
median species-v1 total field of order Carnivora: Canis familiaris
Group default[6]
Sharp zones (foveas)Number of foveas
0
median of 1 relatives in genus Mustela: Mustela putorius
Estimated[7]
Fovea type
area centralis, horizontal streak
Estimated[7]
Night visionActivity pattern
nocturnal
tie ['cathemeral', 'nocturnal'] broken by species-level studies (round-3 tie-break rule 2) (of 5 rows): cathemeral; mixed (nocturnal/crepuscular, cathemeral, crepuscular or diurnal/crepuscular); nocturnal; scotopic
Measured (not re-verified)[8][9][10][11][12]
Rods vs cones
rod-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[8][9][10][11][12]
Motion (flicker fusion)Flicker fusion frequency
76.25 Hz
median of 4 relatives in order Carnivora: Felis catus, Canis lupus, Pagophilus groenlandicus, Canis familiaris
Group default[13][14][15][16]

Related animals

More mammals: all mammals with measured vision data.

Sources

  1. Longcore T. 2023. A compendium of photopigment peak sensitivities and visual spectral response curves of terrestrial wildlife to guide design of outdoor nighttime lighting. Basic Appl Ecol 73:40-50. doi:10.1016/j.baae.2023.09.002. doi.org/10.5281/zenodo.8432720
  2. VPOD in-vivo (MSP / single-cell) lambda max compendium, file scp_cleaned.csv, VPOD GitHub (Frazer et al. 2025 bioRxiv 10.1101/2025.08.22.671864). github.com/VisualPhysiologyDB/visual-physiology-opsin-db/tree/main/scripts_n_notebooks/vpod_ML_workflows/mine_n_match/data_sources/lmax/vpod
  3. Kirk EC, Kay RF 2004. The evolution of high visual acuity in the Anthropoidea. In Anthropoid Origins, Table 1 (behavioural acuity). doi.org/10.1007/978-1-4419-8873-7_20
  4. Heesy CP 2004. On the relationship between orbit orientation and binocular visual field overlap in mammals. Anat Rec 281A:1104, Table 1. doi.org/10.1002/ar.a.20116
  5. Heffner RS, Heffner HE 1992. Visual factors in sound localization in mammals. J Comp Neurol 317:219, Table 1 (via Evo-M1 sensory merge). doi.org/10.1002/cne.903170302
  6. species_v1:Miller & Murphy 1995
  7. Kopania EEK, Clark NL. 2025. Mammalian retinal specializations for high acuity vision evolve in response to both foraging strategies and morphological constraints. Evolution Letters 9: qrae072. Supplementary Tables S1-S2.. doi.org/10.1093/evlett/qrae072
  8. Wilman et al. 2014 EltonTraits 1.0, MamFuncDat.txt. doi.org/10.6084/m9.figshare.3559887.v1
  9. Maor R, Dayan T, Ferguson-Gow H, Jones KE. 2017. Temporal niche expansion in mammals from a nocturnal ancestor after dinosaur extinction. Nature Ecology & Evolution 1:1889-1895. Supplementary Table 1. doi.org/10.1038/s41559-017-0366-5
  10. Jones KE et al. 2009. PanTHERIA: a species-level database of life history, ecology, and geography of extant and recently extinct mammals. Ecology 90:2648. Ecological Archives E090-184. doi.org/10.1890/08-1494.1
  11. Schmitz L, Motani R. 2011. Science 332:705-708, SOM. doi.org/10.1126/science.1200043
  12. Moura et al. 2024. A phylogeny-informed characterisation of global tetrapod traits addresses data gaps and biases. PLoS Biol 22:e3002658. TetrapodTraits v3.0.1.. doi.org/10.5281/zenodo.22536349
  13. Haarlem CS, Hynes C, Jackson AL, Mitchell KJ, O'Connell RG, Healy K. 2026. Pace of ecology drives the tempo of visual perception across the animal kingdom. Nature Ecology & Evolution (doi:10.1038/s41559-026-02994-7). Figshare dataset 10.6084/m9.figshare.30556475. doi.org/10.6084/m9.figshare.30556475
  14. Healy K, McNally L, Ruxton GD, Cooper N, Jackson AL. 2013. Metabolic rate and body size are linked with perception of temporal information. Animal Behaviour 86:685-696. Table 1. doi.org/10.1016/j.anbehav.2013.06.018
  15. Inger R, Bennie J, Davies TW, Gaston KJ. 2014. Potential biological and ecological effects of flickering artificial light. PLoS ONE 9(5): e98631. Table 3. doi.org/10.1371/journal.pone.0098631
  16. Lafitte A, Sordello R, Legrand M, Nicolas V, Obein G, Reyjol Y. 2022. A flashing light may not be that flashy: A systematic review on critical fusion frequencies. PLoS ONE 17(12): e0279718. S10 File (CFF database). doi.org/10.1371/journal.pone.0279718

Every value cites its sources (all sources). Data: catalogue-v1, built 2026-09-29. Accuracy notes: how accurate is this?