Correcting sponge names: nomenclatural update of lower taxa level Porifera.

The online World Porifera Database (WPD), the Porifera part of the World Register of Marine Species (WoRMS), lists virtually all published scientific names of sponges. The names of the WPD (as indeed all names in WoRMS) are guided by the Code of the International Comnission on Zoological Nomenclature (ICZN). The WPD names include all currently accepted as well as original combinations, and a majority of non-accepted non-original combinations. Currently, among the accepted names about 200 original lower taxa combinations were found to be accepted by default, usually varieties or formae, which were given that status in the WPD because there was no sufficient published information to support arguments for or against the accepted status. After 1961, varieties and formae are considered infrasubspecific taxa whose names are not regulated by the Code and the names are unavailable, but prior to that date these trinominal taxa are potential available names. It is the purpose of the present study to evaluate these original default accepted combinations and arrive at an argumented judgement on whether they are to be truly accepted or non-accepted. Furthermore, additional lower taxa name violations of the Code are also included. Overall, there are three categories of names of lower taxa treated here, (1) with combinations, which are judged to be accepted with elevated status as (sub)specific taxa, (2) with combinations judged to be junior synonyms, and (3) with combinations, which are violating articles of the Code. Among the last category there are a small number of varietal taxa described after the 1960 cut-off date, which are unavailable but are proposed to have the original name combination retained, but as new names with authorship and year changed to those of the present article. Also, names found to be unavailable for various reasons (four-name combinations, junior homonyms, phylocode names) are in this category. The following 31 new names are proposed (three of which are junior synonyms of senior accepted names, and an additional three are unavailable names made available by employing the same name combination with the present authorship and year): Aaptos hoshinoi nom.nov., Ancorina nanosclera nom.nov., Axinella kurushima nom.nov., Callyspongia (Cladochalina) desqueyrouxfaundezae nom.nov., Cliona carpenteri subsp. hentscheli nom.nov., Callyspongia (Toxochalina) gustavoi nom.nov., Craniella microspira nom.nov., Dictyaulus romani nom.nov., Grantia breitfussi nom.nov., Haliclona alba subsp. albapontica nom.nov., Haliclona aquaeductus subsp. sebastopolensis nom.nov., Haliclona inflata subsp. vladimiri nom.nov., Haliclona informis subsp. voldomaroi nom.nov., Haliclona palmata subsp. pontuseuxiniensis nom.nov., Haliclona (Gellius) arthuri nom.nov., Haliclona (Gellius) godthaabae nom.nov., Haliclona merguiensis nom.nov., Haliclona senjitanitai nom.nov., Iophon hentscheli nom.nov., Leucandra wilsoni nom.nov., Paraleucilla bassensis nom.nov. (= P. saccharata), Pione carpenteri subsp. hentscheli nom.nov., Psammocinia samaaii nom.nov., Protoschmidtia czerniavskyi nom.nov. (= Metschnikowia tuberculata), Reiswiginella nom.nov., Scalarispongia lamarcki nom.nov., Spheciospongia hentscheli nom.nov., Spongia (Spongia) vonlendenfeldi nom.nov. (= S. (S.) lignosa), Suberites austral nom.nov., Suberites dendyi nom.nov., Suberites simae nom.nov., and Timea levii nom.nov.

Effect of mycalolides isolated from a marine sponge Mycale aff. nullarosette on actin in living cells.

Discovery of novel bioactive compounds is important not only for therapeutic purposes but also for understanding the mechanisms of biological processes. To screen bioactive compounds that affect nuclear morphology in marine organism extracts, we employed a microscopy-based assay using DNA staining of human cancer cells. A crude extract from a marine sponge Mycale aff. nullarosette, collected from the east coast of Japan, induced cellular binucleation. Fractionation of the extract led to the isolation of mycalolides A and B, and 38-hydroxymycalolide B as the active components. Mycalolides have been identified as marine toxins that induce depolymerization of the actin filament. Live cell imaging revealed that low concentrations of mycalolide A produce binucleated cells by inhibiting the completion of cytokinesis. At higher concentrations, however, mycalolide A causes immediate disruption of actin filaments and changes in cell morphology, yielding rounded cells. These results suggest that the completion of cytokinesis is a process requiring high actin polymerization activity. Furthermore, luciferase reporter assays with mycalolide A treatments support the view that the level of globular actin can affect transcription of a serum response gene.

Mycale (Oxymycale) klausjanusorum sp. nov. (Porifera: Demospongiae: Poecilosclerida) from Flores Sea deep water, Indonesia.

A new species of the large genus Mycale Gray, 1867 is described, dredged from approximately 300 m depth in the Flores Sea region between the islands of Salayar and Bahuluang, Central Indonesia, during cruises of the Indonesian-Dutch Snellius II Expedition in 1984. Because its megascleres include oxeas the new species is classified as a member of the subgenus Oxymycale Hentschel, 1929, proposed to be named M. (O.) klausjanusorum sp. nov. to honour renowned colleagues Klaus Rützler and Jean ('Janus') Vacelet. It is characterized by an ectosomal skeleton consisting of bouquets of subtylostyle megascleres protruding beyond an ectosomal tangential confused layer of oxeas, which in turn rests on robust choanosomal bundles of mixed oxea and subtylostyle megascleres. The combination of two categories of megascleres, differentiated not only in size but also in morphology, the larger one of which is arranged in ectosomal bouquets, is a unique feature in the genus Mycale. A high diversity of the microscleres and large upper size of the anisochelae (up to 189 µm) are additional features of the new species. The subgenus Oxymycale is reviewed and its status as a monophyletic group of Mycale is discussed.

Sponges of the family Axinellidae (Porifera: Demospongiae) in Indonesia.

Nine species in five genera of the family Axinellidae, including three new species, Axinella badungensis sp. nov., A. balinensis sp. nov. and Phycopsis pesgalli sp. nov. are recorded from Indonesian waters within the limits of the Western Coral Triangle province. Descriptions and discussion of those species are presented here. Four new combinations, Phakettia arbora (Sim, Kim & Byeon, 1990) comb.nov., P. trachys (De Laubenfels, 1954) comb.nov., Echinoclathria retepora (Lendenfeld, 1887) comb.nov. and Amphimedon hispidula (Ridley, 1884) comb.nov. are also established here. The distributions of species previously described are here extended to the study area with the exception of Phakellia atypica which seems so far restricted to Indonesia.

Cytotoxic activities of hexane, ethyl acetate and butanol extracts of marine sponges from Mauritian Waters on human cancer cell lines.

The ocean is an exceptional source of natural products with many of them exhibiting novel structural features and bioactivity. As one of the most interesting phylum with respect to pharmacological active marine compounds, Poriferas have been investigated widely in the last few decades. A total of 60 organic extracts (hexane, ethyl acetate and butanol) from 20 species of marine sponges from Mauritius were screened at 50µg/ml in an in vitro screening assay against 9 human cancer cell lines. From these tested extracts, many exhibited pronounced cytotoxic effect at least in one of the cell lines and cell type cytotoxic specificity was observed. 27% of ethyl acetate, 11% of hexane and 2% of butanol extracts were found to possess a cytotoxicity ≥75% on 9 different cancer cell lines with the sponges Petrosia sp. 1, Petrosia sp. 2, Pericharax heteroraphis and Jaspis sp. being the most active. Overall, the HL-60cells were much more sensitive to most of the extracts than the other cell lines. We further evaluated the properties of the ethyl acetate (JDE) and hexane extract (JDH) of one sponge, Jaspis sp. on KB cells. JDE displayed a smaller IC(50) than JDH. Clonogenic assay confirmed the antiproliferative effect of both extracts while mitochondrial membrane potential change and microscopic analysis demonstrated extracts-induced apoptosis. Treatment with 100ng/ml of JDE led to a significant increase of cells (24h: 4.02%; 48h: 26.23%) in sub-G1 phase. The cytotoxic properties of the tested extracts from these sponges suggest the presence of compounds with pharmacological potential and are currently undergoing fractionation to isolate the active constituents.

Poecillastrin D: a new cytotoxin of the chondropsin class from marine sponge Jaspis serpentina.

Poecillastrin D (2) was isolated together with poecillastrin C (1) from the deep sea sponge, Japsis serpentina. Its structure was elucidated to be that of a macrolide lactam by spectroscopic methods. These compounds showed potent cytotoxicity against various tumor cell lines.

Extending the record of meroditerpenes from Cacospongia marine sponges.

A new meroditerpene, (+)-isojaspic acid (1), along with two known meroditerpenes, cacospongin D (2) and jaspaquinol (3), have been isolated from a marine sponge Cacospongia. Comprehensive taxonomic identification distinguished this Cacospongia apart from morphologically similar Psammocinia. The absolute stereochemistry of 1 was elucidated on the basis of extensive 1D and 2D NMR techniques and analysis of the optical rotation versus (+)-zonarol (8), (+)-isozonarol (9), (-)-dactylosponol (10), and (+)-hyatellaquinone (11). Furthermore, bioactivity evaluation showed that the meroditerpenes isolated significantly inhibited Staphylococcus epidermidis.