How does the yangtze finless porpoise see?
The yangtze finless porpoise (Neophocaena asiaeorientalis) is a mammal in the order Cetacea. Its eyes belong to the vision type Small prey mammal (UV).
Measured in this species: foveas. 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
- It has one receptor class for colour, so it sees brightness but no hue.
- Its sharpest vision resolves 2.487 cycles per degree: the finest stripe pattern it can tell apart from grey.
- Both eyes see the same 75° in front of it (binocular overlap), where depth is judged best.
- It stops seeing flicker at 60 Hz, against 60 Hz for people in this dataset, so fast motion looks about the same.[12][13]
- Activity pattern: cathemeral.
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.
| Dial | Value | Evidence | Sources |
|---|---|---|---|
| Colour | Colour receptors 1 receptor class: 524 nm (MWS (green)) receptor set of nearest measured relative Tursiops truncatus (same order Cetacea) | Group default | [1] |
| Sharpness | Acuity 2.487 cycles per degree median of 2 relatives in family Phocoenidae: Phocoena phocoena, Phocoenoides dalli | Estimated | [2][3] |
| Field of view | Binocular overlap 75° median of 41 relatives in class Mammalia: Octodon degus, Octodon lunatus, Equus caballus, Ovis aries, Bos taurus, Capra hircus | Group default | [4][5][6][7] |
| Sharp zones (foveas) | Number of foveas 0 fovea_present / area_centralis_type (retinal topography; count 1 = fovea present, 0 = none) | Measured | [8] |
| Fovea type area centralis | Measured | [8] | |
| Night vision | Activity pattern cathemeral mode of 1 relatives in genus Neophocaena: Neophocaena phocaenoides | Estimated | [9][10] |
| Rods vs cones mixed | Estimated | [9][10] | |
| Motion (flicker fusion) | Flicker fusion frequency 60 Hz median of 21 relatives in class Mammalia: Rattus norvegicus, Cavia porcellus, Mus musculus, Felis catus, Macaca mulatta, Macaca nemestrina | Group default | [11][12][13][14] |
Related animals
- Amazon river dolphin same vision type
- Beluga whale same vision type
- Grey whale same vision type
- Harbor porpoise same vision type
- Killer whale same vision type
- Minke whale same vision type
More mammals: all mammals with measured vision data.
Sources
- Frazer SA, Baghalian M, et al. 2024. Discovering genotype-phenotype relationships with machine learning and the Visual Physiology Opsin Database (VPOD). GigaScience 13:giae073; VPOD v1.3 data release. doi.org/10.5281/zenodo.19051998
- de Sousa AA et al. 2022. A natural history of vision loss: insight from evolution for human visual function. Neurosci Biobehav Rev 134:104550 (mmc, acuity compilation). doi.org/10.1016/j.neubiorev.2022.104550
- Kirk & Kay 2004 Table 2 (anatomical acuity). doi.org/10.1007/978-1-4419-8873-7_20
- 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
- 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
- Vega-Zuniga T, Medina FS, Fredes F, et al. 2013. Does nocturnality drive binocular vision? Octodontine rodents as a case study. PLoS ONE 8: e84199.. doi.org/10.1371/journal.pone.0084199
- Vega-Zuniga T, Medina FS, Marín G, Letelier JC, Palacios AG, Němec P, Schleich CE, Mpodozis J. (2017). Selective binocular vision loss in two subterranean caviomorph rodents: Spalacopus cyanus and Ctenomys talarum. Scientific reports
- 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
- Wilman et al. 2014 EltonTraits 1.0, MamFuncDat.txt. doi.org/10.6084/m9.figshare.3559887.v1
- 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
- Haarlem CS, Hynes C, Jackson AL, Mitchell KJ, O'Connell RG, Healy K. 2026. Pace of ecology drives the tempo of visual perception across the animal kingdom. Nature Ecology & Evolution (doi:10.1038/s41559-026-02994-7). Figshare dataset 10.6084/m9.figshare.30556475. doi.org/10.6084/m9.figshare.30556475
- 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
- 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
- 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?