How does the reindeer see?
The reindeer (Rangifer tarandus) is a mammal in the order Artiodactyla. Its eyes belong to the vision type Grazing ungulate panorama.
Measured in this species: colour 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
- It has two colour receptor classes (a dichromat): reds and greens fall on one axis, as in red-green colour blindness in people.
- Its sharpest vision resolves 18.48 cycles per degree: the finest stripe pattern it can tell apart from grey.
- Its eyes cover about 350° around the head, with 45° seen by both eyes at once.
- It stops seeing flicker at 60 Hz, against 60 Hz for people in this dataset, so fast motion looks about the same.[14][15]
- Activity pattern: cathemeral.
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.
| Dial | Value | Evidence | Sources |
|---|---|---|---|
| Colour | Colour receptors 2 receptor classes: 439 nm (VS/SWS (violet)), 542 nm (LWS (long)) measured in this species | Measured (not re-verified) | [1][2] |
| Sharpness | Acuity 18.48 cycles per degree median of 1 relatives in family Cervidae: Dama dama | Estimated | [3] |
| Field of view | Binocular overlap 45° median of 4 relatives in order Artiodactyla: Ovis aries, Bos taurus, Capra hircus, Sus scrofa | Group default | [4][5] |
| Total field of view 350° group default: median total field of vision type V04 within phylum Chordata in species-v1: Equus caballus | Group default | [6] | |
| Sharp zones (foveas) | Number of foveas 0 median of 9 relatives in order Artiodactyla: Bos taurus, Bubalus bubalis, Capra hircus, Ovis aries, Camelus dromedarius, Vicugna pacos | Group default | [7] |
| Fovea type anakatabatic area, area centralis, horizontal streak | Group default | [7] | |
| Night vision | Activity pattern cathemeral tie ['cathemeral', 'diurnal'] broken by the broader category (round-3 tie-break rule 3: cathemeral > crepuscular > nocturnal > diurnal) (of 7 rows): cathemeral; diurnal; diurnal/crepuscular; mesopic; ultradian | Measured (not re-verified) | [8][9][10][11][12] |
| Rods vs cones mixed nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated | Derived | [8][9][10][11][12] | |
| Motion (flicker fusion) | Flicker fusion frequency 60 Hz median of 2 relatives in order Artiodactyla: Ovis aries, Sus scrofa | Group default | [13] |
Related animals
- Cow same vision type
- Pig same vision type
- Sheep same vision type
- Goat same vision type
- Arabian camel same vision type
- Giraffe same vision type
More mammals: all mammals with measured vision data.
Sources
- Murphy MJ, Westerman EL. 2022. Evolutionary history limits species' ability to match colour sensitivity to available habitat light. Proc R Soc B 289:20220612. Electronic supplementary Table S1. doi.org/10.1098/rspb.2022.0612
- 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
- Veilleux CC, Kirk EC 2014. Visual acuity in mammals. Brain Behav Evol 83:43, Supplementary Table 1 (cleaned CSV in Evo-M1-Trait-Data). doi.org/10.1159/000357830
- 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
- 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
- species_v1:Timney & Keil 1992
- 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
- Borges R, Johnson WE, O'Brien SJ, Gomes C, Heesy CP, Antunes A (2018) Adaptive genomic evolution of opsins reveals that early mammals flourished in nocturnal environments. BMC Genomics 19:121
- Wilman et al. 2014 EltonTraits 1.0, MamFuncDat.txt. doi.org/10.6084/m9.figshare.3559887.v1
- 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
- Schmitz L, Motani R. 2011. Science 332:705-708, SOM. doi.org/10.1126/science.1200043
- 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
- 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
- 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
- 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
Every value cites its sources (all sources). Data: catalogue-v1, built 2026-09-29. Accuracy notes: how accurate is this?