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How does the ambon damelfish see?

The ambon damelfish (Pomacentrus amboinensis) is a fish in the order Perciformes. Its eyes belong to the vision type Shallow-water fish tetrachromat.

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 ambon damelfish (Pomacentrus amboinensis), catalogue-v1
DialValueEvidenceSources
ColourColour receptors
2 receptor classes: 502 nm (MWS (green)), 560 nm (LWS (long))
receptor set of nearest measured relative Pomacentrus melanochir (same genus Pomacentrus)
Estimated[1][2]
SharpnessAcuity
1.36 cycles per degree
median of 1 behavioural rows (method priority rule)
Measured[3]
Field of viewBinocular overlap
32.85°
group default: median of tier-A values in vision type V18 within phylum Chordata (2 species: Danio rerio, Notemigonus crysoleucas)
Group default[4]
Sharp zones (foveas)Number of foveas
0
mode of species-v1 relatives in order Perciformes: Toxotes jaculatrix
Group default[5]
Fovea type
ventrotemporal area (high rgc density)
Group default[5]
Night visionActivity pattern
diurnal
mode of 1 rows (of 1 rows): diurnal
Measured[6]
Rods vs cones
cone-dominated
nocturnal -> rod-dominated; crepuscular / cathemeral / mixed -> mixed; diurnal -> cone-dominated
Derived[6]
Motion (flicker fusion)Flicker fusion frequency
89 Hz
median of 1 relatives in family Pomacentridae: Acanthochromis polyacanthus
Estimated[7]

Related animals

More fish: all fish with measured vision data.

Sources

  1. Schweikert LE, Fitak RR, Caves EM, Sutton TT, Johnsen S. 2018. Spectral sensitivity in ray-finned fishes: diversity, ecology and shared descent. J Exp Biol 221:jeb189761. Table S1. doi.org/10.1242/jeb.189761
  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, 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. Pita D, Moore BA, Tyrrell LP, Fernandez-Juricic E. 2015. Vision in two cyprinid fish: implications for collective behavior. PeerJ 3:e1113.. doi.org/10.7717/peerj.1113
  5. species_v1:Temple et al. 2010
  6. Froese R. & Pauly D. (eds). FishBase, snapshot v25.04 (morphmet, morphdat, species, families tables), distributed as parquet by C. Boettiger for rfishbase.. fishbase.org
  7. 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
  8. 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
  9. 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?