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. 2021 Jan 18;19:8. doi: 10.1186/s12915-020-00921-1

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© The Author(s) 2020

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Phylogenetic placement of Ostiactis pearseae. Phylogenetic reconstruction resulting from maximum likelihood analysis using PhyML (RaxML results not shown, but congruent) of the concatenated dataset of three mitochondrial (12S rDNA, 16S rDNA, COIII) and two partial nuclear markers (18S and 28S rDNA). Dotted boxes indicate actiniarian suborders; colored triangles and green box indicate actiniarian superfamilies; empty boxes and arrows indicate relevant actiniarian clades. Position of Ostiactis pearseae specimens from Pescadero Basin vent communities is highlighted in the orange box; the position of an additional sea anemone (unidentified morphospecies Kadosactinidae ‘sp.B’) is indicated by the light orange box. Bootstrap resampling values are indicated by black circles; only support values > 80% are shown