The DOI matches its Crossref record; 3 of the 3 references it cites were found in a registry or an index.
Resolution of ray-finned fish phylogeny and timing of diversification
Abstract
Ray-finned fishes make up half of all living vertebrate species. Nearly all ray-finned fishes are teleosts, which include most commercially important fish species, several model organisms for genomics and developmental biology, and the dominant component of marine and freshwater vertebrate faunas. Despite the economic and scientific importance of ray-finned fishes, the lack of a single comprehensive phylogeny with corresponding divergence-time estimates has limited our understanding of the evolution and diversification of this radiation. Our analyses, which use multiple nuclear gene sequences in conjunction with 36 fossil age constraints, result in a well-supported phylogeny of all major ray-finned fish lineages and molecular age estimates that are generally consistent with the fossil record. This phylogeny informs three long-standing problems: specifically identifying elopomorphs (eels and tarpons) as the sister lineage of all other teleosts, providing a unique hypothesis on the radiation of early euteleosts, and offering a promising strategy for resolution of the “bush at the top of the tree” that includes percomorphs and other spiny-finned teleosts. Contrasting our divergence time estimates with studies using a single nuclear gene or whole mitochondrial genomes, we find that the former underestimates ages of the oldest ray-finned fish divergences, but the latter dramatically overestimates ages for derived teleost lineages. Our time-calibrated phylogeny reveals that much of the diversification leading to extant groups of teleosts occurred between the late Mesozoic and early Cenozoic, identifying this period as the “Second Age of Fishes.”
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Some molecular phylogenetic studies failed to support Siluriphysi monophyly.
“Nonetheless, some molecular phylogenetic studies (e.g., Figures S2, S4, and S5 in Hughes et al.’s study, and in Near et al.’s and Melo et al.’s studies)54,55,56 failed to support Siluriphysi monophyly.”
From A genomic compendium of hundreds of teleost fishes reveals their evolutionary landscape (2026) · cites this paper as [55]
Although molecular phylogenetic studies have demonstrated frequent discordance between molecular data and morphological expectations, the monophyly of Siluriphysi has generally been maintained in traditional interpretations from early single-locus analyses to recent multiple genomic-scale loci, primarily to conform to morphological predictions.
“Although numerous molecular phylogenetic studies have demonstrated frequent discordance between molecular data and morphological expectations, the monophyly of Siluriphysi has generally been maintained in traditional interpretations, from early single-locus analyses48 to recent multiple genomic-scale loci,49,50,51,52,53,54,55,56 primarily to conform to morphological predictions.”
From A genomic compendium of hundreds of teleost fishes reveals their evolutionary landscape (2026) · cites this paper as [55]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
RAxML-VI-HPC: maximum likelihood-based phylogenetic analyses with thousands of taxa and mixed models
Stamatakis, A. (2006) · Bioinformatics · doi:10.1093/bioinformatics/btl446 · Cited by 15,582
Relaxed Phylogenetics and Dating with Confidence
Drummond, A. J., Ho, S. Y. W., Phillips, M. J., & Rambaut, A. (2006) · PLoS Biology · doi:10.1371/journal.pbio.0040088 · Cited by 6,463
Impacts of the Cretaceous Terrestrial Revolution and KPg extinction on mammal diversification
Meredith, R. W., Janečka, J. E., Gatesy, J., Ryder, O. A., Fisher, C. A., Teeling, E. C., Goodbla, A., Eizirik, E., Simão, T. L. L., Stadler, T., et al. (2011) · Science · doi:10.1126/science.1211028 · Cited by 1,464
Flagged first, then by citations
Research works printed but not linked: 43
- RC Thomson, HB Shaffer, Rapid progress on the vertebrate tree of life. BMC Biol 8, 19 (2010). · DOI
- WN Eschmeyer, R Fricke Catalog of fishes (California Academy of Sciences, San Francisco, 2012).
- JS Nelson Fishes of the World (John Wiley, 4th Ed, Hoboken, 2006).
- SJ Hackett, et al., A phylogenomic study of birds reveals their evolutionary history. Science 320, 1763–1768 (2008). · DOI · Paper page
- MLJ Stiassny, EO Wiley, GD Johnson, MR de Carvalho Assembling the Tree of Life, eds J Cracraft, MJ Donoghue (Oxford Univ Press, New York), pp. 410–429 (2004). · DOI
- IA Hurley, et al., A new time-scale for ray-finned fish evolution. Proc Biol Sci 274, 489–498 (2007).
- GV Lauder, KF Liem, The evolution and interrelationships of the actinopterygian fishes. Bull Mus Comp Zool 150, 95–197 (1983).
- C Patterson, DE Rosen, Review of ichthyodectiform and other Mesozoic teleost fishes and the theory and practice of classifying fossils. Bull Am Mus Nat Hist 158, 85–172 (1977).
- C Patterson, Comments on basal teleosts and teleostean phylogeny, by Gloria Arratia. Copeia 1998, 1107–1109 (1998). · DOI
- G Arratia, Basal teleosts and teleostean phylogeny. Paleo Ichth 7, 5–168 (1997).
- G Arratia, Basal teleosts and teleostean phylogeny: Response to C. Patterson. Copeia 1998, 1109–1113 (1998). · DOI
- WL Fink Ontogeny and Systematic of Fishes, eds HG Moser, et al. (Allen Press, Lawrence, KS), pp. 202–206 (1984).
- GD Johnson, C Patterson Interrelationships of Fishes, eds MLJ Stiassny, LR Parenti, GD Johnson (Academic, San Diego), pp. 251–332 (1996). · DOI
- RM McDowall, CP Burridge, Osteology and relationships of the southern freshwater lower euteleostean fishes. Zoosystematics and Evolution 87, 7–185 (2011). · DOI
- G Nelson The Hierarch of Life, eds B Fernholm, K Bremer, H Jôrnvall (Elsevier, Amsterdam), pp. 325–336 (1989).
- JG Inoue, M Miya, K Tsukamoto, M Nishida, A mitogenomic perspective on the basal teleostean phylogeny: Resolving higher-level relationships with longer DNA sequences. Mol Phylogenet Evol 20, 275–285 (2001). · DOI
- HL Lê, G Lecointre, R Perasso, A 28S rRNA-based phylogeny of the gnathostomes: First steps in the analysis of conflict and congruence with morphologically based cladograms. Mol Phylogenet Evol 2, 31–51 (1993). · DOI
- ME Alfaro, et al., Nine exceptional radiations plus high turnover explain species diversity in jawed vertebrates. Proc Natl Acad Sci USA 106, 13410–13414 (2009). · DOI
- F Santini, LJ Harmon, G Carnevale, ME Alfaro, Did genome duplication drive the origin of teleosts? A comparative study of diversification in ray-finned fishes. BMC Evol Biol 9, 164 (2009). · DOI
- NB Ishiguro, M Miya, M Nishida, Basal euteleostean relationships: A mitogenomic perspective on the phylogenetic reality of the “Protacanthopterygii”. Mol Phylogenet Evol 27, 476–488 (2003). · DOI
- JA Lopez, WJ Chen, G Ortí, Esociform phylogeny. Copeia 2004, 449–464 (2004). · DOI
- J Li, et al., Phylogenetic position of the enigmatic Lepidogalaxias salamandroides with comment on the orders of lower euteleostean fishes. Mol Phylogenet Evol 57, 932–936 (2010). · DOI
- M Miya, et al., Major patterns of higher teleostean phylogenies: A new perspective based on 100 complete mitochondrial DNA sequences. Mol Phylogenet Evol 26, 121–138 (2003). · DOI
- PC Wainwright, et al., The evolution of pharyngognathy: A phylogenetic and functional appraisal of the pharyngeal jaw key innovation in Labroidei and beyond. Syst Biol, 2012). · DOI
- B Li, et al., RNF213, a new nuclear marker for acanthomorph phylogeny. Mol Phylogenet Evol 50, 345–363 (2009). · DOI
- WL Smith, MT Craig, Casting the percomorph net widely: The importance of broad taxonomic sampling in the search for the placement of serranid and percid fishes. Copeia 2007, 35–55 (2007). · DOI
- M Miya, et al., Evolutionary history of anglerfishes (Teleostei: Lophiiformes): A mitogenomic perspective. BMC Evol Biol 10, 58 (2010). · DOI
- K Vandepoele, W De Vos, JS Taylor, A Meyer, Y Van de Peer, Major events in the genome evolution of vertebrates: Paranome age and size differ considerably between ray-finned fishes and land vertebrates. Proc Natl Acad Sci USA 101, 1638–1643 (2004). · DOI
- BG Gardiner, The relationships of the palaeoniscid fishes, a review based on new specimens of Mimia and Moythomasia from Upper Devonian of Western Australia. Bull Brit Mus (Nat Hist) Geol 37, 173–428 (1984).
- JG Inoue, M Miya, K Tsukamoto, M Nishida, Basal actinopterygian relationships: A mitogenomic perspective on the phylogeny of the “ancient fish”. Mol Phylogenet Evol 26, 110–120 (2003). · DOI
- CH Li, GQ Lu, G Ortí, Optimal data partitioning and a test case for ray-finned fishes (Actinopterygii) based on ten nuclear loci. Syst Biol 57, 519–539 (2008). · DOI
- JY Poulsen, et al., Higher and lower-level relationships of the deep-sea fish order Alepocephaliformes (Teleostei: Otocephala) inferred from whole mitogenome sequences. Biol J Linn Soc Lond 98, 923–936 (2009). · DOI
- JM Waters, et al., Phylogenetic placement of retropinnid fishes: Data set incongruence can be reduced by using asymmetric character state transformation costs. Syst Biol 51, 432–449 (2002). · DOI
- TJ Near, et al., Nuclear gene-inferred phylogenies resolve the relationships of the enigmatic Pygmy Sunfishes, Elassoma (Teleostei: Percomorpha). Mol Phylogenet Evol 63, 388–395 (2012). · DOI
- M Nakatani, M Miya, K Mabuchi, K Saitoh, M Nishida, Evolutionary history of Otophysi (Teleostei), a major clade of the modern freshwater fishes: Pangaean origin and Mesozoic radiation. BMC Evol Biol 11, 177 (2011). · DOI · Paper page
- Y Yamanoue, M Miya, JG Inoue, K Matsuura, M Nishida, The mitochondrial genome of spotted green pufferfish Tetraodon nigroviridis (Teleostei: Tetraodontiformes) and divergence time estimation among model organisms in fishes. Genes Genet Syst 81, 29–39 (2006). · DOI
- C Patterson Fossil Record 2, ed MJ Benton (Chapman and Hall, London), pp. 621–656 (1993).
- M Friedman, LC Sallan, Five hundred million years of extinction and recovery: A Phanerozoic survey of large-scale diversity patterns in fishes. Palaeontology 55, 707–742 (2012). · DOI
- P Janvier Early Vertebrates (Oxford Univ Press, New York, 1996). · DOI · Paper page
- CH Li, G Ortí, G Zhang, GQ Lu, A practical approach to phylogenomics: The phylogeny of ray-finned fish (Actinopterygii) as a case study. BMC Evol Biol 7, 44 (2007). · DOI
- R Chaudhary, MS Bansal, A Wehe, D Fernández-Baca, O Eulenstein, iGTP: A software package for large-scale gene tree parsimony analysis. BMC Bioinformatics 11, 574 (2010). · DOI
- J Sukumaran, MT Holder, DendroPy: A Python library for phylogenetic computing. Bioinformatics 26, 1569–1571 (2010). · DOI
- AJ Drummond, A Rambaut, BEAST: Bayesian evolutionary analysis by sampling trees. BMC Evol Biol 7, 214 (2007). · DOI
Cited by
Sorted by citations
Genome-wide interrogation advances resolution of recalcitrant groups in the tree of life
Arcila, D., Ortí, G., Vari, R., Armbruster, J. W., Stiassny, M. L. J., Ko, K. D., Sabaj, M. H., Lundberg, J., Revell, L. J., & Betancur-R., R. (2017) · Nature Ecology & Evolution · doi:10.1038/s41559-016-0020 · Cited by 243
Genome structures resolve the early diversification of teleost fishes
Parey, E., Louis, A., Montfort, J., Bouchez, O., Roques, C., Iampietro, C., Lluch, J., Castinel, A., Donnadieu, C., Desvignes, T., et al. (2023) · Science · doi:10.1126/science.abq4257 · Cited by 87
Colonization of the deep sea by fishes
Priede, I. G., & Froese, R. (2013) · Journal of Fish Biology · doi:10.1111/jfb.12265 · Cited by 81
Davesne, D., Meunier, F. J., Schmitt, A. D., Friedman, M., Otero, O., & Benson, R. B. J. (2019) · Biological Reviews · doi:10.1111/brv.12505 · Cited by 57
Self-citationA genomic compendium of hundreds of teleost fishes reveals their evolutionary landscape
Song, Y., Yuan, Z., Fang, C., Zhang, S., Yang, L., Hu, M., Seim, I., Liu, S., Tian, X., Wang, C., et al. (2026) · The Innovation · doi:10.1016/j.xinn.2025.101177 · Cited by 3
Sudasinghe, H., Matschiner, M., Britz, R., Conway, K. W., Tan, H. H., Salzburger, W., Peichel, C. L., & Rüber, L. (2026) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.2614605123
Metadata
- Authors
- Near, T. J., Eytan, R. I., Dornburg, A., Kuhn, K. L., Moore, J. A., Davis, M. P., Wainwright, P. C., Friedman, M., & Smith, W. L.
- Affiliations
- Department of Ecology and Evolutionary Biology and Peabody Museum of Natural History, Yale University, New Haven, CT 06520;
- Wilkes Honors College, Florida Atlantic University, Jupiter, FL 33458;
- Department of Zoology, Fishes, The Field Museum, Chicago, IL 60605;
- Department of Evolution and Ecology, University of California, Davis, CA 95616; and
- Department of Earth Sciences, University of Oxford, Oxford OX1 3AN, United Kingdom
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2012-08-06
- Volume
- 109
- Issue
- 34
- Pages
- 13698-13703
- ISSN
- 0027-8424
- 1091-6490
- Cited by
- 912
- References
- 3
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review