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How does the Coquerel's sifaka see?

The Coquerel's sifaka (Propithecus coquereli) is a mammal in the order Primates. Its eyes belong to the vision type Day dichromat mammal.

Measured in this species: foveas and night vision. 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 Coquerel's sifaka (Propithecus coquereli), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
1 receptor class: 558 nm (LWS (long))
receptor set of nearest measured relative Avahi laniger (same family Indriidae)
Estimated[1][2]
SharpnessAcuity
43.25 cycles per degree
median of 28 relatives in order Primates: Aotus azarae, Alouatta caraya, Aotus trivirgatus, Callithrix jacchus, Sapajus apella, Chlorocebus aethiops
Group default[3][4][5][6][7]
Field of viewBinocular overlap
137°
median of 6 relatives in order Primates: Otolemur crassicaudatus, Cephalopachus bancanus, Aotus trivirgatus, Saimiri sciureus, Macaca mulatta, Homo sapiens
Group default[8][9]
Total field of view
200°
median species-v1 total field of order Primates: Homo sapiens
Group default[10]
Sharp zones (foveas)Number of foveas
0
fovea_present / area_centralis_type (retinal topography; count 1 = fovea present, 0 = none)
Measured[11]
Fovea type
area centralis
Measured[11]
Night visionActivity pattern
diurnal
mode of 6 rows (of 6 rows): diurnal
Measured (not re-verified)[3][12][13][14][15]
Rods vs cones
cone-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[3][12][13][14][15]
Motion (flicker fusion)Flicker fusion frequency
69 Hz
median of 3 relatives in order Primates: Macaca mulatta, Macaca nemestrina, Homo sapiens
Group default[16][17][18]

Related animals

More mammals: all mammals 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. Borges R, Johnson WE, O'Brien SJ, Gomes C, Heesy CP, Antunes A (2018) Adaptive genomic evolution of opsins reveals that early mammals flourished in nocturnal environments. BMC Genomics 19:121
  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. Kirk EC, Kay RF 2004. The evolution of high visual acuity in the Anthropoidea. In Anthropoid Origins, Table 1 (behavioural acuity). doi.org/10.1007/978-1-4419-8873-7_20
  6. Kirk & Kay 2004 Table 2 (anatomical acuity). doi.org/10.1007/978-1-4419-8873-7_20
  7. Veilleux CC, Kirk EC 2014. Visual acuity in mammals. Brain Behav Evol 83:43, Supplementary Table 1 (cleaned CSV in Evo-M1-Trait-Data). doi.org/10.1159/000357830
  8. Heesy CP 2004. On the relationship between orbit orientation and binocular visual field overlap in mammals. Anat Rec 281A:1104, Table 1. doi.org/10.1002/ar.a.20116
  9. Heffner RS, Heffner HE 1992. Visual factors in sound localization in mammals. J Comp Neurol 317:219, Table 1 (via Evo-M1 sensory merge). doi.org/10.1002/cne.903170302
  10. species_v1:Campbell & Green 1965
  11. Kopania EEK, Clark NL. 2025. Mammalian retinal specializations for high acuity vision evolve in response to both foraging strategies and morphological constraints. Evolution Letters 9: qrae072. Supplementary Tables S1-S2.. doi.org/10.1093/evlett/qrae072
  12. Wilman et al. 2014 EltonTraits 1.0, MamFuncDat.txt. doi.org/10.6084/m9.figshare.3559887.v1
  13. Maor R, Dayan T, Ferguson-Gow H, Jones KE. 2017. Temporal niche expansion in mammals from a nocturnal ancestor after dinosaur extinction. Nature Ecology & Evolution 1:1889-1895. Supplementary Table 1. doi.org/10.1038/s41559-017-0366-5
  14. Jones KE et al. 2009. PanTHERIA: a species-level database of life history, ecology, and geography of extant and recently extinct mammals. Ecology 90:2648. Ecological Archives E090-184. doi.org/10.1890/08-1494.1
  15. 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
  16. 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
  17. 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
  18. 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?