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How does the ring-necked pheasant see?

The ring-necked pheasant (Phasianus colchicus) is a bird in the order Galliformes. Its eyes belong to the vision type Panoramic grain-eater and wader.

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 ring-necked pheasant (Phasianus colchicus), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
4 receptor classes: 418 nm (VS/SWS (violet)), 455 nm (SWS (blue)), 507 nm (MWS (green)), 569 nm (LWS (long))
receptor set of nearest measured relative Gallus gallus (same family Phasianidae)
Estimated[1][2]
SharpnessAcuity
12.9 cycles per degree
median of 1 anatomical-ganglion rows (method priority rule)
Measured[3]
Field of viewBinocular overlap
27.5°
median of 133 relatives in class Aves: Accipiter cooperii, Spatula clypeata, Mareca penelope, Anas platyrhynchos, Ardeola ralloides, Baeolophus bicolor
Group default[4][5][6][7][8][9][10][11][12]
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[13][14]
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[15][16][17]
Fovea type
single central fovea (displaced dorso-temporally from retinal centre)		Group default[15][16][17]
Night visionActivity pattern
diurnal
mode of 7 rows (of 7 rows): diurnal; not_nocturnal
Measured (not re-verified)[18][19][20][21][22][23][24]
Rods vs cones
cone-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[18][19][20][21][22][23][24]
Motion (flicker fusion)Flicker fusion frequency
104 Hz
median of 1 relatives in family Phasianidae: Gallus gallus
Estimated[25]

Related animals

More birds: all birds with measured vision data.

Sources

  1. 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
  2. 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
  3. Caves EM, Brandley NC, Johnsen S (2018) Visual acuity and the evolution of signals. Trends Ecol Evol 33:358-372. Supplementary Tables S1-S3.. doi.org/10.1016/j.tree.2018.03.001
  4. 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
  5. 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
  6. Vision and foraging in structurally complex habitats: common moorhens (Gallinula chloropus). Ecology and Evolution 2026, e74060.. doi.org/10.1002/ece3.74060
  7. Pecsics T, Csorgo T. 2023. Ornis Hungarica 31(2):110-124. doi.org/10.2478/orhu-2023-0023
  8. 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
  9. Potier S, Duriez O, Cunningham GB, et al. 2018. J Exp Biol 221:jeb177295. doi.org/10.1242/jeb.177295
  10. 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
  11. 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
  12. 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
  13. species_v1:Martin & Young 1983
  14. species_v1:Martin 1994
  15. 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
  16. 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
  17. 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
  18. Anderson SR, Wiens JJ. 2017. Out of the dark: 350 million years of conservatism and evolution in diel activity patterns in vertebrates. Evolution 71:1944-1959. Dryad doi:10.5061/dryad.fg700. doi.org/10.5061/dryad.fg700
  19. 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
  20. Light conditions and the evolution of the visual system in birds (figshare dataset, SupplementaryDataset1). doi.org/10.6084/m9.figshare.22116371.v3
  21. 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
  22. 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
  23. 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
  24. 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
  25. 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
  26. 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
  27. 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?