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How does the Eurasian skylark see?

The Eurasian skylark (Alauda arvensis) 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 skylark (Alauda arvensis), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
4 receptor classes: 367.5 nm (UVS), 443 nm (SWS (blue)), 502.5 nm (MWS (green)), 570 nm (LWS (long))
receptor set of nearest measured relative Serinus canaria (same order Passeriformes)
Group default[1][2]
Ultraviolet
yes: at least one receptor peaks in the ultraviolet		Group default
SharpnessAcuity
16.95 cycles per degree
median of 2 behavioural rows (method priority rule)
Measured[3][4]
Field of viewBinocular overlap
35°
median of 26 relatives in order Passeriformes: Baeolophus bicolor, Corvus albus, Corvus brachyrhynchos, Corvus corax, Corvus corone, Corvus frugilegus
Group default[5][6]
Sharp zones (foveas)Number of foveas
1
median of 29 relatives in order Passeriformes: Cardinalis cardinalis, Passerina cyanea, Cyanocitta cristata, Junco hyemalis, Melospiza melodia, Melozone crissalis
Group default[7][8]
Fovea type
single central fovea (displaced dorso-temporally from retinal centre)		Group default[7][8]
Night visionActivity pattern
diurnal
mode of 7 rows (of 7 rows): diurnal; not_nocturnal; photopic
Measured (not re-verified)[9][10][11][12][13]
Rods vs cones
cone-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[9][10][11][12][13]
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[14][15][16][17]

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. 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. 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. Caves EM, Fernandez-Juricic E, Kelley LA (2024) Ecological and morphological correlates of visual acuity in birds. J Exp Biol 227(2): jeb246063. Supplementary Table S1.. doi.org/10.1242/jeb.246063
  5. 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
  6. 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
  7. 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
  8. 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
  9. 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
  10. Light conditions and the evolution of the visual system in birds (figshare dataset, SupplementaryDataset1). doi.org/10.6084/m9.figshare.22116371.v3
  11. 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
  12. Schmitz L, Motani R. 2011. Science 332:705-708, SOM. doi.org/10.1126/science.1200043
  13. 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
  14. 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
  15. 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
  16. 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
  17. 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?