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How does the Eurasian jay see?

The Eurasian jay (Garrulus glandarius) is a bird in the order Passeriformes. Its eyes belong to the vision type UV songbird, parrot and hummingbird.

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 Eurasian jay (Garrulus glandarius), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
2 receptor classes: 497 nm (MWS (green)), 565 nm (LWS (long))
receptor set of nearest measured relative Corvus frugilegus (same family Corvidae)
Estimated[1]
SharpnessAcuity
30 cycles per degree
median of 1 behavioural rows (method priority rule)
Measured[2]
Field of viewBinocular overlap
16.5°
median of 8 relatives in family Corvidae: Corvus albus, Corvus brachyrhynchos, Corvus corax, Corvus corone, Corvus frugilegus, Coloeus monedula
Estimated[3][4]
Total field of view
328.5°
median total field (measured, or 360 - blind area) of relatives in family Corvidae: Corvus brachyrhynchos, Aphelocoma californica
Estimated[3]
Sharp zones (foveas)Number of foveas
1
median of 1 relatives in family Corvidae: Cyanocitta cristata
Estimated[5]
Fovea type
single central fovea (displaced dorso-temporally from retinal centre)		Estimated[5]
Night visionActivity pattern
diurnal
mode of 6 rows (of 6 rows): diurnal; not_nocturnal
Measured (not re-verified)[6][7][8][9][10][11]
Rods vs cones
cone-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[6][7][8][9][10][11]
Motion (flicker fusion)Flicker fusion frequency
100 Hz
median of 7 relatives in order Passeriformes: Passer domesticus, Taeniopygia guttata, Molothrus ater, Sturnus vulgaris, Cyanistes caeruleus, Ficedula albicollis
Group default[12][13][14][15]

Other senses

Related animals

More birds: all birds 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. 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
  3. 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
  4. 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
  5. 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
  6. 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
  7. Light conditions and the evolution of the visual system in birds (figshare dataset, SupplementaryDataset1). doi.org/10.6084/m9.figshare.22116371.v3
  8. 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
  9. 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
  10. 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
  11. 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
  12. 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
  13. 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
  14. 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
  15. 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?