Convergent camouflage and the non-monophyly of ‘seadragons’ (Syngnathidae: Teleostei): suggestions for a revised taxonomy of syngnathids
2010; Wiley; Volume: 39; Issue: 6 Linguagem: Inglês
10.1111/j.1463-6409.2010.00449.x
ISSN1463-6409
AutoresNerida G. Wilson, Greg W. Rouse,
Tópico(s)Ichthyology and Marine Biology
ResumoZoologica ScriptaVolume 39, Issue 6 p. 551-558 Convergent camouflage and the non-monophyly of 'seadragons' (Syngnathidae: Teleostei): suggestions for a revised taxonomy of syngnathids Nerida G. Wilson, Nerida G. WilsonSearch for more papers by this authorGreg W. Rouse, Greg W. RouseSearch for more papers by this author Nerida G. Wilson, Nerida G. WilsonSearch for more papers by this authorGreg W. Rouse, Greg W. RouseSearch for more papers by this author First published: 10 September 2010 https://doi.org/10.1111/j.1463-6409.2010.00449.xCitations: 19 Corresponding authors: Nerida G. Wilson, The Australian Museum, 6 College Street, Sydney NSW 2010 Australia; and Greg W. Rouse, Marine Biology Research Division, Scripps Institution of Oceanography, University of California San Diego, 9500 Gilman Drive, La Jolla, CA 92093-0202, USA. E-mails: [email protected] and [email protected] Read the full textAboutPDF ToolsRequest permissionExport citationAdd to favoritesTrack citation ShareShare Give accessShare full text accessShare full-text accessPlease review our Terms and Conditions of Use and check box below to share full-text version of article.I have read and accept the Wiley Online Library Terms and Conditions of UseShareable LinkUse the link below to share a full-text version of this article with your friends and colleagues. Learn more.Copy URL Share a linkShare onEmailFacebookTwitterLinkedInRedditWechat Abstract Wilson, N. G. & Rouse, G. W. (2010). Convergent camouflage and the non-monophyly of 'seadragons' (Syngnathidae: Teleostei): suggestions for a revised taxonomy of syngnathids. —Zoologica Scripta, 39, 551–558. The phylogeny and classification of the charismatic Syngnathidae (e.g. pipefish, seahorses) has not been comprehensively examined to date. In particular, we assessed morphological hypotheses that previously suggested the three 'seadragon' genera (Phycodurus, Phyllopteryx, Haliichthys) do not form a monophyletic group. We used three mitochondrial markers to investigate evolutionary relationships within Syngnathidae, and demonstrated that Phycodurus + Phyllopteryx formed a clade that excluded Haliichthys, indicating the elaborate appendages used for camouflage have evolved independently. A time-calibrated tree revealed the divergence of true seadragons as coincident with other kelp-associated fauna. We found evidence for the resurrection of neglected subfamily names, and recovered Doryrhampinae, Nerophinae, Soleganthinae, Phyllopteryginae, Sygnathoidinae and Haliichthyinae as clades. Even after removing these groups from what is currently recognized as Syngnathinae, we showed that the remaining members of Syngnathinae are not monophyletic. In the light of this information, some conclusions about the diversity of reproductive strategies found within 'Syngnathinae' need to be re-examined and further revision of syngnathid classification is needed. Supporting Information Figure S1. Maximum likelihood phylogeny of syngnathids based on three mitochondrial genes, with support tested by 1000 bootstrap replicates. Support below 50 is not shown unless it appears alongside greater support at a node representative of relationships among subfamilial rankings. These nodes also show support values under Bayesian inference (posterior probabilities) and maximum parsimony (jackknife). *Support is for a node that does not include Haliichthys. Square brackets surround H. grayi, indicating likely contamination of Cytb in NCBI. Figure S2. beast (Bayesian evolutionary analysis by sampling trees)-generated chromogram showing relationships among Syngnathidae. 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