Systema Naturae includes representatives of every major lineage of the animal phylum Cnidaria.  However, Linnaeus did not classify the members of the phylum as is now done, and the diversity of the group is not well represented.  We contrast the Linnaean perspective on cnidarian diversity with the modern, phylogenetic perspective.  For each order, we detail diversity at the family level, providing phylogenetic context where possible.

Sea anemones (order Actiniaria) are among the most diverse and successful members of the anthozoan subclass Hexacorallia, occupying benthic marine habitats across all depths and latitudes. Actiniaria comprises approximately 1,200 species of solitary and skeleton-less polyps and lacks any anatomical synapomorphy. Although monophyly is anticipated based on higher-level molecular phylogenies of Cnidaria, to date, monophyly has not been explicitly tested and at least some hypotheses on the diversification of Hexacorallia have suggested that actiniarians are para- or poly-phyletic. Published phylogenies have demonstrated the inadequacy of existing morphological-based classifications within Actiniaria. Superfamilial groups and most families and genera that have been rigorously studied are not monophyletic, indicating conflict with the current hierarchical classification. We test the monophyly of Actiniaria using two nuclear and three mitochondrial genes with multiple analytical methods. These analyses are the first to include representatives of all three currently-recognized suborders within Actiniaria. We do not recover Actiniaria as a monophyletic clade: the deep-sea anemone Boloceroides daphneae, previously included within the infraorder Boloceroidaria, is resolved outside of Actiniaria in several of the analyses. We erect a new genus and family for B. daphneae, and rank this taxon incerti ordinis. Based on our comprehensive phylogeny, we propose a new formal higher-level classification for Actiniaria composed of only two suborders, Anenthemonae and Enthemonae. Suborder Anenthemonae includes actiniarians with a unique arrangement of mesenteries (members of Edwardsiidae and former suborder Endocoelantheae). Suborder Enthemonae includes actiniarians with the typical arrangement of mesenteries for actiniarians (members of former suborders Protantheae, Ptychodacteae, and Nynantheae and subgroups therein). We also erect subgroups within these two newly-erected suborders. Although some relationships among these newly-defined groups are still ambiguous, morphological and molecular results are consistent enough to proceed with a new higher-level classification and to discuss the putative functional and evolutionary significance of several morphological attributes within Actiniaria.

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Acontia-nematocyst-dense, thread-like extensions of the mesenterial filaments-are the characteristic feature of the actiniarian group Acontiaria. Phylogenetic analyses have shown that acontiate taxa form a clade that also includes some taxa without acontia. We analyse five molecular markers from 85 actiniarians to explore the phylogenetic relationships among families in Acontiaria, including acontiate species assigned to other higher taxa and species without acontia that have been allied to Acontiaria. Based on our results, we redefine the group to accommodate those lineages that have lost acontia, and formalize it as superfamily Metridioidea. Based on stable and well supported clades, we resurrect Phelliidae and Amphianthidae, redefine Kadosactinidae and Actinoscyphiidae, and move two species to new genera: that previously termed Sagartiogeton erythraios belongs in Jasonactis gen. nov.; and that previously termed Anthosactis pearseae belongs in Ostiactis gen. nov., type genus of Ostiactinidae fam. nov. We also synonymized Halcampoididae and Halcampidae (as Halcampidae) and Andvakiidae and Isophelliidae (as Andvakiidae). The results of our phylogenetic analyses indicate that the diagnostic morphological characters used in the family-level taxonomy of acontiate actiniarians such as the nematocysts of the acontia, the marginal sphincter muscle, and mesenteries divisible into macro-and microcnemes, have to be revisited, as these features are highly homoplasious.

Anthozoans (e.g., corals, anemones) are an ecologically important and diverse group of marine metazoans that occur from shallow to deep waters worldwide. However, our understanding of the evolutionary relationships among the ~7,500 species within this class is hindered by the lack of phylogenetically informative markers that can be reliably sequenced across a diversity of taxa. We designed and tested 16,306 RNA baits to capture 720 ultraconserved element loci and 1,071 exon loci. Library preparation and target enrichment were performed on 33 taxa from all orders within the class Anthozoa. Following Illumina sequencing and Trinity assembly, we recovered 1,774 of 1,791 targeted loci. The mean number of loci recovered from each species was 638 ± 222, with more loci recovered from octocorals (783 ± 138 loci) than hexacorals (475 ± 187 loci). Parsimony informative sites ranged from 26 to 49% for alignments at differing hierarchical taxonomic levels (e.g., Anthozoa, Octocorallia, Hexacorallia). The per cent of variable sites within each of three genera (Acropora, Alcyonium, and Sinularia) for which multiple species were sequenced ranged from 4.7% to 30%. Maximum-likelihood analyses recovered highly resolved trees with topologies matching those supported by other studies, including the monophyly of the order Scleractinia. Our results demonstrate the utility of this target-enrichment approach to resolve phylogenetic relationships from relatively old to recent divergences. Redesigning the baits with improved affinities to capture loci within each subclass will provide a valuable toolset to address systematic questions, further our understanding of the timing of diversifications and help resolve long-standing controversial relationships in the class Anthozoa.

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46Anthozoans (e.g., corals, anemones) are an ecologically important and diverse group of 47 marine metazoans that occur from shallow to deep waters worldwide. However, our 48 understanding of the evolutionary relationships among the ~7500 species within this class is 49 hindered by the lack of phylogenetically informative markers that can be reliably sequenced 50 across a diversity of taxa. We designed and tested 16,308 RNA baits to capture 720 51Ultraconserved Element loci and 1,071 exon loci. Library preparation and target enrichment was 52 performed on 33 taxa from all orders within the class Anthozoa. Following Illumina sequencing 53and Trinity assembly, we recovered 1,774 of 1,791 targeted loci. The mean number of loci 54 recovered from each species was 638 ± 222, with more loci recovered from octocorals (783 ± 55 138 loci) than hexacorals (475 ±187 loci). Phylogenetically informative sites ranged from 26-56 49% for alignments at differing hierarchical taxonomic levels (e.g., Anthozoa, Octocorallia, 57 Hexacorallia). The percent of variable sites within each of three genera (Acropora, Alcyonium, 58and Sinularia) for which multiple species were sequenced ranged from 4.7-30%. Maximum 59 likelihood analyses recovered highly resolved trees with topologies matching those supported by 60 other studies, including the monophyly of the order Scleractinia. Our results demonstrate the 61 utility of this target-enrichment approach to resolve phylogenetic relationships from relatively 62 old to recent divergences. Re-designing the baits with improved affinities to capture loci within 63 each sub-class will provide a valuable toolset to address systematic questions and further our 64

Sea anemones of the genus Aiptasia Gosse, 1858 are conspicuous members of shallow-water environments worldwide and serve as a model system for studies of cnidarian-dinoflagellate symbiosis. However, to date there have been no comprehensive analyses investigating the systematics of the group. In addition, previously published phylogenetic studies of sea anemones have shown that the genus is not monophyletic. Herein we revise the genus Aiptasia and the family Aiptasiidae Carlgren, 1924 using newly-collected material. We find that the formerly-named A. pallida (Agassiz in Verrill, 1864) (now Exaiptasia pallida comb. nov.) encompasses a single, widespread species from the tropics and subtropics; we erect a new genus, Exaiptasia gen. nov., for this species primarily based on cnidae, mode of asexual reproduction and symbionts. We also find morphological evidence that supports splitting A. mutabilis into two species: A. couchii (Cocks, 1851) and A. mutabilis. In addition, we find Bellactis Dube, 1983 (formerly placed within Sagartiidae Gosse, 1858) and Laviactis gen. nov. (formerly known Ragactis Andres, 1883, whose familial placement was previously uncertain) belonging within Aiptasiidae. Aiptasiidae is a morphologically homogeneous family whose members (those species in genera Aiptasia, Aiptasiogeton Schmidt, 1972, Bartholomea Duchassaing de Fombressin & Michelotti, 1864, Bellactis, Exaiptasia gen. nov., and Laviactis gen. nov.) are characterized by ectodermal longitudinal muscles in the distal column, rows of cinclides in mid-column, microbasic b-mastigophores in the column, and acontia with basitrichs and microbasic p-amastigophores.