SLICE™ (active ingredient 0.2% emamectin benzoate (EMB)), a feed premix developed by Schering‐Plough Animal Health for the control of sea lice on cultured salmonids, is registered for use in several countries and is being prescribed on an emergency basis in Canada and the United States. The concentration of EMB in feed administered to farmed salmon ranges from 1 to 25 μg g−1. To determine the acute toxicity of the compound to juvenile and adult American lobster (Homarus americanus), commercial salmon feed was coated with SLICE™ at a range of concentrations and provided to the animals for 7 d in the laboratory. The LC50 is estimated to be 644 μg g−1 (95% CI=428, 1275) for adult lobsters and >589 μg g−1 for stage V and VI juvenile lobsters. The consumption of medicated pellets by adult lobsters decreased significantly with increasing concentration of EMB. Adult lobsters that died during the study had a significantly greater concentration of emamectin B1a in their muscle tissue than those that survived. These results support the conclusion that salmon feed medicated with EMB at the concentrations used by the aquaculture industry is unlikely to pose an acute lethal threat to adult and small juvenile American lobsters.

Table 1. Species used in analysis. For each species, the scientific name, type of organism, type of data, number of sequences, and reference of original publication is shown. SpeciesBroad Taxon Type of Data # sequences Original publication Bryopsis sp. Green Algae cpDNA 66 Krellwitz et al. (2001) Gracilaria tikvahiae Red Algae cpDNA 20 Gurgel et al.(2004) Xerula furfuracea Fungi nuDNA 41 Yang et al.(2009) & Petersen and Hughes (2010) & Hao et al.(2016) Sphagnum bartlettianum Bryophyta cpDNA + nuDNA 12 Shaw et al.(2005) Acer rubrum Angiosperm cpDNA 38 McLachlan et al.(2005) Apios americana Angiosperm nuDNA 18 Joly & Bruneau (2004) Dicerandra spp Angiosperm cpDNA 30 Oliveira et al.(2007) Fagus grandifolia Angiosperm cpDNA 23 McLachlan et al.(2005) Liquidambar styraciflua Angiosperm cpDNA 109 Morris et al.(2008) Prunus spp Angiosperm cpDNA 226 Shaw & Small (2005) Tilia americana Angiosperm cpDNA 297 McCarthy and Mason-Gamer (2016) Trillium cuneatum Angiosperm cpDNA 281 Gonzales et al.(2008) Uniola paniculata Angiosperm cpDNA 131 Hodel & Gonzales (2013) Bugula neritina Bryozoa mtDNA 30 McGovern & Hellberg (2003) Daphnia obtusa Crustacean mtDNA 36 Penton et al.(2004) Emerita talpoida Crustacean mtDNA 4 Tam et al.(1996) Farfantepenaeus aztecus Crustacean mtDNA 76 McMillen-Jackson and Bert (2003) Litopenaeus setiferus Crustacean mtDNA 92 McMillen-Jackson and Bert (2003) & Maggioni et al. (2001) &Vazquez-Bader et al.(2004) & Bremer et al.(2010) Pagarus longicarpus Crustacean mtDNA 67 Young et al.(2002) Pagarus pollicaris Crustacean mtDNA 13 Young et al.(2002) Busycon sinistrum Gastropod mtDNA 31 Wise et al.(2004) Lampsilis altilis Mollusk mtDNA 5 Roe et al.(2001) Lampsilis australis Mollusk mtDNA 5 Roe et al.(2001) Lampsilis ovata Mollusk mtDNA 2 Roe et al.(2001) & Campbell et al.(2005) Lampsilis perovalis Mollusk mtDNA 5 Roe et al.(2001) Lampsilis teres Mollusk mtDNA 2 Roe et al.(2001) & Lydeard et al.(2000) Spisula solidissima Mollusk mtDNA 52 Hare and Weinberg (2005) Ambystoma tigrinum Amphibian mtDNA 56 Church et al.(2003) Desmognathus wrightii Amphibian mtDNA 29 Crespi et al.(2003) Eumeces fasciatus Amphibian mtDNA 82 Howes et al.(2006) Eurycea bislineata Amphibian mtDNA 56 Kozak et al.(2006) Eurycea cirrigera Amphibian mtDNA 251 Kozak et al.(2006) Eurycea junaluska Amphibian mtDNA 6 Kozak et al.(2006) Eurycea multiplicata Amphibian mtDNA 46 Bonett & Chippindale (2004) Eurycea tymerensis Amphibian mtDNA 16 Bonett & Chippindale (2004) Eurycea wilderae Amphibian mtDNA 129 Kozak et al.(2006)

Aim:The "sexy shrimp" Thor amboinensis is currently considered a single circumtropical species. However, the tropical oceans are partitioned by hard and soft barriers to dispersal, providing ample opportunity for allopatric speciation. Herein, we test the null hypothesis that T. amboinensis is a single global species, reconstruct its global biogeographical history, and comment on population-level patterns throughout the Tropical Western Atlantic.Location: Coral reefs in all tropical oceans.Methods: Specimens of Thor amboinensis were obtained through field collection and museum holdings. We used one mitochondrial (COI) and two nuclear (NaK, enolase) gene fragments for global species delimitation and phylogenetic analyses (n = 83 individuals, 30 sample localities), while phylogeographical reconstruction in the TWA was based on COI only (n = 303 individuals, 10 sample localities).Results: We found evidence for at least five cryptic lineages (9%-22% COI pairwise sequence divergence): four in the Indo-West Pacific and one in the Tropical Western Atlantic. Phylogenetic reconstruction revealed that endemic lineages from Japan and the South Central Pacific are more closely related to the Tropical Western Atlantic lineage than to a co-occurring lineage that is widespread throughout the Indo-West Pacific. Concatenated and species tree phylogenetic analyses differ in the placement of an endemic Red Sea lineage and suggest alternate dispersal pathways into the Atlantic. Phylogeographical reconstruction throughout the Tropical Western Atlantic reveals little genetic structure over more than 3,000 km.Main conclusions: Thor amboinensis is a species complex that has undergone a series of allopatric speciation events and whose members are in secondary contact in the Indo-West Pacific. Nuclear-and mitochondrial-gene phylogenies show evidence of introgression between lineages inferred to have been separated more than 20 Ma. Phylogenetic discordance between multi-locus analyses suggest that T. amboinensis originated in the Tethys sea and dispersed into the Atlantic and Indo-West Pacific through the Tethys seaway or, alternatively, originated in the Indo-

No abstract

Haloclavidae Verrill, 1899 is a family of burrowing sea anemones grouped within the superfamily Actinioidea (Rafinesque, 1815). Currently, it includes 30 species in 10 genera. Characters given for this family in descriptions of its taxa have not been consistent, with numerous exceptions to the expectations of the familial diagnosis. Previous phylogenetic analyses have shown that Haloclavidae is potentially a polyphyletic group, but resolution of relationships of the few representatives of Haloclavidae included in analyses has been problematic. Here we address questions of monophyly and affinity of Haloclavidae using three mitochondrial and two nuclear markers. We assess the monophyly of Haloclavidae in the context of all major lineages of Actiniaria Hertwig, 1882, emphasizing diversity of superfamily Actinioidea. We use parsimony-based character optimization to interpret the distribution of key traits in the superfamily. We find that Haloclavidae is not monophyletic and propose two new families, Peachiidae fam. nov. and Harenactidae fam. nov., while also retaining some species in the family Haloclavidae, so that taxonomy better reflects relationships and diversity of the group. In addition, we redescribe a species within the newly created Peachiidae, Peachia chilensis Carlgren, 1931. We use recent larval samples obtained in Antofagasta, Chile, and the histological slides from the original description to redescribe P. chilensis, to provide a complete account of cnidae, external, and internal morphology. Finally, we compare P. chilensis to other burrowing anemones found in Chile and provide an understanding of the genus Peachia that reflects recent phylogenetic perspective on diversity of anemones previously assigned to family Haloclavidae.