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How does the green frog see?

The green frog (Lithobates clamitans) is a amphibian in the order Anura. Its eyes belong to the vision type Amphibian motion detector.

Measured in this species: night vision and motion (flicker fusion). One measured dial: a value other than colour or sharpness is measured in this species; colour and sharpness are not measured here. 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 frog (Lithobates clamitans), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
3 receptor classes: 432.5 nm (VS/SWS (violet)), 502 nm (MWS (green)), 575 nm (LWS (long))
receptor set of nearest measured relative Lithobates catesbeianus (same genus Lithobates)
Estimated[1][2]
SharpnessAcuity
2.8 cycles per degree
median of 1 relatives in genus Lithobates: Lithobates pipiens
Estimated[3]
Field of viewNo value in the catalogue.
Sharp zones (foveas)No value in the catalogue.
Night visionActivity pattern
cathemeral
mode of 4 rows (of 4 rows): cathemeral; diurnal and nocturnal; nocturnal
Measured (not re-verified)[4][5][6][7]
Rods vs cones
mixed
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[4][5][6][7]
Motion (flicker fusion)Flicker fusion frequency
21 Hz
median of 1 rows (no bright-light flag) (behavioural/whole-eye ERG rows; all rows: [21.0])
Measured[8]

Related animals

More amphibians: all amphibians 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. Yovanovich CAM, Koskela SM, Nevala N, Kondrashev SL, Kelber A, Donner K. 2017. The dual rod system of amphibians supports colour discrimination at the absolute visual threshold. Phil Trans R Soc B 372:20160066.. doi.org/10.1098/rstb.2016.0066
  3. 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
  4. Oliveira et al. 2017. AmphiBIO, a global database for amphibian ecological traits. Sci Data 4:170123.. doi.org/10.6084/m9.figshare.4644424.v5
  5. 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
  6. Schott RK, Fujita MK, Streicher JW, Gower DJ, Thomas KN, Loew ER, et al. (28 authors, last Bell RC). 2024. Diversity and evolution of frog visual opsins: spectral tuning and adaptation to distinct light environments. Mol Biol Evol 41:msae049.. doi.org/10.1093/molbev/msae049
  7. 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
  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
  9. 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

Every value cites its sources (all sources). Data: catalogue-v1, built 2026-09-29. Accuracy notes: how accurate is this?