How does the emu see?
The emu (Dromaius novaehollandiae) is a bird in the order Casuariiformes. Its eyes belong to the vision type Panoramic grain-eater and wader.
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 4 colour receptor classes; people have 3.
- Its sharpest vision resolves 30.2 cycles per degree: the finest stripe pattern it can tell apart from grey.
- Its eyes cover about 338° around the head, with 27.5° seen by both eyes at once.
- It stops seeing flicker at 88.5 Hz, against 60 Hz for people in this dataset, so fast motion looks about 1.5 times slower to it.[28][29]
- Activity pattern: diurnal.
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 4 receptor classes: 405 nm (VS/SWS (violet)), 449 nm (SWS (blue)), 504 nm (MWS (green)), 567 nm (LWS (long)) measured in this species | Measured | [1][2] |
| Sharpness | Acuity 30.2 cycles per degree allometry (Aves): log10(acuity_cpd) = intercept + slope * log10(eye_axial_length_mm); slope 0.9017, intercept 0.1397, R2 0.453, n 99 (fitted in this script; fitted range [4.36, 39.81] mm); eye_axial_length_mm 30.65 mm | Estimated | [3][4][5][6] |
| Field of view | Binocular overlap 27.5° median of 133 relatives in class Aves: Accipiter cooperii, Spatula clypeata, Mareca penelope, Anas platyrhynchos, Ardeola ralloides, Baeolophus bicolor | Group default | [7][8][9][10][11][12][13][14][15] |
| Total field of view 338° group default: median total field of vision type V10 within phylum Chordata in species-v1: Columba livia, Scolopax minor | Group default | [16][17] | |
| Sharp zones (foveas) | Number of foveas 1 median of 48 relatives in class Aves: Branta canadensis, Cardinalis cardinalis, Passerina cyanea, Zenaida macroura, Cyanocitta cristata, Junco hyemalis | Group default | [18][19][20] |
| Fovea type single central fovea (displaced dorso-temporally from retinal centre) | Group default | [18][19][20] | |
| Night vision | Activity pattern diurnal mode of 7 rows (of 7 rows): cathemeral; diurnal; not_nocturnal | Measured (not re-verified) | [21][4][22][23][2][24][25] |
| Rods vs cones cone-dominated nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated | Derived | [21][4][22][23][2][24][25] | |
| Motion (flicker fusion) | Flicker fusion frequency 88.5 Hz median of 17 relatives in class Aves: Bubo virginianus, Melopsittacus undulatus, Passer domesticus, Taeniopygia guttata, Columba livia, Calypte anna | Group default | [26][27][28][29][30] |
Related animals
- Rock pigeon same vision type
- Chicken same vision type
- Canada goose same vision type
- Common ostrich same vision type
- Mallard same vision type
- Manx shearwater same vision type
More birds: all birds with measured vision data.
Sources
- Lind O, Mitkus M, Olsson P, Kelber A. 2014. Ultraviolet vision in birds: the importance of transparent eye media. Proc R Soc B 281:20132209. Table 1. doi.org/10.1098/rspb.2013.2209
- 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
- Ausprey I.J. & Ritland S. 2024. Eye morphology contributes to the ecology and evolution of the avian tree of life [Dataset]. Dryad. Digitised Table 7 of Ritland S. 1982, The allometry of the vertebrate eye, PhD dissertation, University of Chicago. Paper: Ausprey 2024 J Anim Ecol doi:10.1111/1365-2656.14141. doi.org/10.5061/dryad.3xsj3txq7
- Light conditions and the evolution of the visual system in birds (figshare dataset, SupplementaryDataset1). doi.org/10.6084/m9.figshare.22116371.v3
- Olsson P, Lind O, Mitkus M, Delhey K, Kelber A. 2021. Lens and cornea limit UV vision of birds - a phylogenetic perspective. J Exp Biol 224:jeb243129. doi.org/10.1242/jeb.243129
- Vertebrate eye-size compilation in Thomas et al. 2020 Dryad deposit (Thomas_vertebrates.csv). Primary sources: Howland et al. 2004 (n=313); Schmitz & Wainwright 2011 (n=265); Schmitz et al. 2013 (n=237); Hall 2008 (n=116); Veilleux & Kirk 2014 (n=91); Hall & Heesy 2011 (n=88); Liu et al. 2012 (n=66); Werner & Seifan 2006 (n=62); Lisney & Collin 2007 (n=46). doi.org/10.5061/dryad.1zcrjdfq7
- Cantlay JC, Martin GR, McClelland SC, Potier S, O'Brien MF, Fernandez-Juricic E, Bond AL, Portugal SJ 2023. Binocular vision and foraging in ducks, geese and swans (Anatidae). Proc R Soc B 290: 20231213. ESM full data set (figshare collection 6781097).. doi.org/10.1098/rspb.2023.1213
- Lucas EA, Martin GR, Rocamora G, Portugal SJ. 2024. A seabird's eye view: visual fields of some seabirds (Laridae and Procellariidae) from tropical latitudes. The Science of Nature (Naturwissenschaften) 111. ESM 1.. doi.org/10.1007/s00114-024-01926-4
- Vision and foraging in structurally complex habitats: common moorhens (Gallinula chloropus). Ecology and Evolution 2026, e74060.. doi.org/10.1002/ece3.74060
- Pecsics T, Csorgo T. 2023. Ornis Hungarica 31(2):110-124. doi.org/10.2478/orhu-2023-0023
- Portugal SJ, Ozturk R, Murn CP, Potier S, Martin GR. 2023. Current Biology 33:R1142-R1143. doi.org/10.1016/j.cub.2023.09.016
- Potier S, Duriez O, Cunningham GB, et al. 2018. J Exp Biol 221:jeb177295. doi.org/10.1242/jeb.177295
- Potier S, Roulin A, Martin GR, Portugal SJ, Bonhomme V, Bouchet T, de Romans R, Meyrier E, Kelber A. 2023. Binocular field configuration in owls: the role of foraging ecology. Proc R Soc B 290: 20230664. Data figshare.. doi.org/10.1098/rspb.2023.0664
- Tyrrell LP, Moore BA, Loftis C, Fernandez-Juricic E 2017 (data 2017). The hawk-eyed songbird: retinal morphology, eye shape, and visual fields of an aerial insectivore. Am Nat 189(6). Dryad doi:10.5061/dryad.n7140.. doi.org/10.1086/691404
- Tyrrell LP, Fernandez-Juricic E 2017. Avian binocular vision: it's not just about what birds can see, it's also about what they can't. PLoS ONE 12(3): e0173235. S1 Table.. doi.org/10.1371/journal.pone.0173235
- species_v1:Martin & Young 1983
- species_v1:Martin 1994
- Moore BA, Tyrrell LP, Pita D, Bininda-Emonds ORP, Fernandez-Juricic E 2017. Does retinal configuration make the head and eyes of foveate birds move? Sci Rep 7: 38406. Appendix 1.. doi.org/10.1038/srep38406
- Potier S, Mitkus M, Bonadonna F, Duriez O, Isard P-F, Dulaurent T, Mentek M, Kelber A 2017. Eye size, fovea, and foraging ecology in accipitriform raptors. Brain Behav Evol 90: 232-242. Supplementary material (Tables S1, S2).. doi.org/10.1159/000479783
- Rodrigues T, Matter MM, Chiodini A, et al. 2026. Foveal vision in fast-flying birds hunting on the wing. bioRxiv 2026.06.05.730304. doi.org/10.64898/2026.06.05.730304
- Angielczyk KD, Schmitz L 2014. Nocturnality in synapsids predates the origin of mammals by over 100 million years. Proc R Soc B 281: 20141642. Dryad doi:10.5061/dryad.1v8kj.. doi.org/10.1098/rspb.2014.1642
- Choiniere JN, Neenan JM, Schmitz L, Ford DP, Chapelle KEJ, Balanoff AM, Sipla JS, Georgi JA, Walsh SA, Norell MA, Xu X, Clark JM, Benson RBJ. 2021. Evolution of vision and hearing modalities in theropod dinosaurs. Science 372:610-613. doi:10.1126/science.abe7941. Data: https://osf.io/teq73/. doi.org/10.1126/science.abe7941
- Wilman H, Belmaker J, Simpson J, de la Rosa C, Rivadeneira MM, Jetz W. 2014. EltonTraits 1.0: species-level foraging attributes of the world's birds and mammals. Ecology 95:2027. BirdFuncDat.txt. doi.org/10.6084/m9.figshare.3559887.v1
- Schmitz & Motani 2011. Nocturnality in dinosaurs inferred from scleral ring and orbit morphology. Science 332:705. Comparative data redeposited in Xing et al. 2020 supplementary information (Zenodo).. doi.org/10.5281/zenodo.3591994
- 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
- Boström JE, Dimitrova M, Canton C, Håstad O, Qvarnström A, Ödeen A. 2016. Ultra-rapid vision in birds. PLoS ONE 11(3): e0151099. S1 Table. doi.org/10.1371/journal.pone.0151099
- 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
- 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?