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How does the green sea turtle see?

The green sea turtle (Chelonia mydas) is a reptile in the order not recorded. Its eyes belong to the vision type Diurnal reptile tetrachromat.

Measured in this species: colour, night vision and motion (flicker fusion). Measured core: measured values on at least 3 of the 6 dials. 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 green sea turtle (Chelonia mydas), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
4 receptor classes: 360 nm (UVS), 440 nm (SWS (blue)), 502 nm (MWS (green)), 562 nm (LWS (long))
measured in this species
Measured[1]
Ultraviolet
yes: at least one receptor peaks in the ultraviolet
Measured
SharpnessNo value in the catalogue.
Field of viewNo value in the catalogue.
Sharp zones (foveas)Number of foveas
2
group default: mode of tier-A values in vision type V14 within phylum Chordata (1 species: Anolis carolinensis)
Group default[2][3]
Fovea type
central fovea, temporal
Group default[2][3]
Night visionActivity pattern
cathemeral
mode of 4 rows (of 4 rows): arrhythmic/cathemeral; cathemeral; diurnal
Measured (not re-verified)[4][1][5][6]
Rods vs cones
mixed
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[4][1][5][6]
Motion (flicker fusion)Flicker fusion frequency
40 Hz
median of 1 bright-light rows (behavioural/whole-eye ERG rows; all rows: [40.0])
Measured[7]

Related animals

More reptiles: all reptiles 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. Rasys AM, Wegerski A, Trainor PA, Hufnagel RB, Menke DB, Lauderdale JD. 2024. Dynamic changes in ocular shape during human development and its implications for retina fovea formation. BioEssays : news and reviews in molecular, cellular and developmental biology 46(1):e2300054. doi.org/10.1002/bies.202300054
  3. species_v1:Fleishman et al. 1988 / Makaretz & Levine 1980
  4. 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
  5. Oskyrko O, Mi C, Meiri S, Du W. 2024. ReptTraits: a comprehensive dataset of ecological traits in reptiles. Scientific Data 11 (doi:10.1038/s41597-024-03079-5). Dataset v1-2 (includes Meiri 2018 lizard traits). doi.org/10.6084/m9.figshare.24572683.v4
  6. 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
  7. 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
  8. 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?