Sponges in the verongiid genus Pseudoceratina Carter are well-known producers of bioactive secondary metabolites. Chemical screening of a Tongan P. cf. verrucosa Bergquist using NMR highlighted the presence of aromatic natural products. Subsequent extraction and purification of P. cf. verrucosa yielded a new bromotyrosine, purpuramine R (1), that exhibits moderate (MIC 16 µg/mL) antibacterial activity against Gram-positive Staphylococcus aureus. The E-geometry of the oxime was confirmed using a combination of NMR and computational approaches. Additionally, computational conformational analysis indicates that purpuramine R adopts a hairpin orientation, stabilized by intramolecular hydrogen and halogen bonds. Knowledge of this stabilized conformation can inform synthetic approaches to make analogues of the purpuramines for future SAR studies.

Sponges are an important component of shallow- and deep-water ecosystems enhancing eukaryotic biodiversity via diverse endo- and epibiota and by providing three dimensional habitats for benthic invertebrates and fishes. Sponge biodiversity is particularly high in the waters around New Zealand (Southwest Pacific), where we collected two shallow- and two deep-water sponge species (Tedania sp., Suberea meandrina, Farrea raoulensis, Artemisina sp.) for ex-situ incubation experiments to measure processing of dissolved organic matter (DOM). Several sponge species take up DOM and make it available to other fauna as detritus or as sponge biomass, a process known as sponge loop. However, it is unknown whether the selected sponge species are able to consume dissolved organic carbon (DOC) and/or total dissolved nitrogen (TDN). We measured DOC and TDN fluxes and linked it to the bacterial communities of the sponge holobiont to address research hypothesis 1. It stated that high-microbial abundance (HMA) sponges consume more DOM than low-microbial abundance (LMA) sponges. Changes in fluorescent dissolved organic matter (FDOM) over time were investigated to address research hypothesis 2. It proposed that the fluorescence intensity Fmax of fluorophores decreased in incubations that showed a significant loss in DOM. We assessed the biochemical and phospholipid-derived fatty acids (PLFAs) composition of sponge tissue to address hypothesis 3. It suggested that the PLFLA composition of sponges differs between sponge classes. Finally, we tried to better understand the role of these sponges in nutrient cycling around New Zealand by combining data from all analyses. Based on the community composition of the sponge-associated bacteria, we classified Tedania sp., S. meandrina, and Artemisina sp. as HMA sponges and F. raoulensis as LMA sponge. We did not measure a significant DOC flux and only the release of TDN by Tedania sp. was significantly different from 0 mu mol TDN g org. C-1 d-1. The presence of four fluorophores were detected in the FDOM pool: 2 tryptophan- and protein-like fluorophores (C1, C2), 1 humic-like fluorophore (C3), and 1 tyrosine-like fluorophore (C4). However, we could not validate hypothesis 2, because Fmax of C1 decreased significantly in S. meandrina incubations, whereas Fmax of C2 grew in the same incubations. Fmax of C3 increased in Tedania sp. incubations, in which Fmax of C4 decreased. In comparison, Fmax of C4 in S. meandrina rose. The PLFA composition of sponge tissue was dominated by long-chain fatty acids, saturated fatty acids, and monosaturated fatty acids, and most PLFAs were sponge- and bacteria-specific. We could not confirmed hypothesis 3, either, because the PLFA composition of the

Sponges are an important component of deep-water ecosystems enhancing eukaryotic biodiversity by hosting diverse endo- and epibiota and providing three dimensional habitats for benthic invertebrates and fishes. As holobionts they are important hosts of microorganisms which are involved in carbon and nitrogen cycling. While increasing exploration of deep-water habitats results in new sponge species being discovered, little is known about their physiology and role in nutrient fluxes. Around New Zealand (Southwest Pacific), the sponge biodiversity is particularly high, and we selected six deep-sea sponge genera (Saccocalyx, Suberites, Tedania, Halichondria/Dendoricella, Lissodendoryx) and a member of the Sceptrulophora order for in-situ and ex-situ experiments. We investigated the biochemical composition of the sponges, measured oxygen consumption and inorganic nutrient fluxes, as well as bacterial and phospholipid-derived fatty acid (PLFA) compositions. Our aim was to assess differences in fluxes and fatty acid composition among sponges and linking their bacterial communities to nitrogen cycling processes. All sponges excreted nitrite and ammonia. Nitrate and phosphate excretion were independent of phylum affiliation (Demospongiae, Hexactinellida). Nitrate was excreted by Halichondria/Dendoricella and Lissodendoryx, whereas Suberites, Tedania, and Sceptrulophora consumed it. Phosphate was excreted by Sceptrulophora and Halichondria/Dendoricella and consumed by all other sponges. Oxygen consumption rates ranged from 0.17 to 3.56 +/- 0.60 mmol O2 g C-1 d- 1. The PLFA composition was very sponge-genera dependent and consisted mostly of long-chain fatty acids. Most PLFAs were sponge-specific, followed by bacteria-specific PLFAs, and others. All sponges, except for Suberites, were low-microbial abundance (LMA) sponges whose bacterial community composition was dominated by Proteobacteria, Bacteroidota, Planctomycetota, and Nitrospinota. Suberites consisted of high-microbial abundance (HMA) sponges with Proteobacteria, Chloroflexota, Acidobacteriota, and Actinobacteriota as dominant bacteria. Based on the inorganic nitrogen flux measurements, we identified three types of nitrogen cycling in the sponges: In type 1, sponges (Dendoricella spp. indet., Lissodendoryx) respired aerobically and ammonificated organic matter (OM) to ammonium, fixed N2 to ammonium, and nitrified aerobically heterotrophically produced ammonium to nitrate and nitrite. In type 2, sponges (Halichondria sp., Sceptrulophora, Suberites, Tedania) respired OM aerobically and ammonificated it to ammonium. They also reduced nitrate anaerobically to

Biogenic habitats are foundational habitats for species assemblages and drive a range of ecosystem functions. The Hauraki Gulf/Tiikapa Moana is the most intensively used coastal area in Aotearoa/New Zealand, and decades of commercial fishing, sedimentation and industrialization have degraded biogenic habitats in the Gulf. In response, the marine spatial plan 'Sea Change' includes proposals to create new and extend existing marine protected areas (MPAs) and restrict the area open to mobile bottom-impact fishing methods to conserve and help the recovery of biogenic habitats. To assess the benefits of different spatial planning scenarios for biogenic habitats, information on their spatial distribution is needed, but data limitations are a significant challenge. Here, an approach is detailed that maximized the information extracted from limited species occurrence data, by incorporating expert knowledge to develop and evaluate models of biogenic habitat-forming taxa. Ensemble habitat suitability models (using boosted regression tree and random forest models) were created for 20 biogenic habitat groups. Using withheld data for validation, area under curve (AUC) scores ranged from 0.58 to 0.95 and true skill statistics (TSS) ranged from 0.37 to 0.84, though three models were further evaluated as insufficient representations of known ecological habitats by expert assessors. Models produced here provide substantially increased information to inform progress on implementation of the Sea Change plan. Two stakeholder processes have been held, resulting in the development of spatial plans for bottom trawl mitigation that are currently under public consultation. Systematic surveys that gather abundance and high-resolution environmental data should be a priority to improve the utility of predictive models and inform future management processes in the Hauraki Gulf, and funding has been allocated to support additional data collection to determine the effectiveness of spatial management measures in the Hauraki Gulf.

Sponges are an important component of shallow- and deep-water ecosystems enhancing eukaryotic biodiversity via diverse endo- and epibiota and by providing three dimensional habitats for benthic invertebrates and fishes. Sponge biodiversity is particularly high in the waters around New Zealand (Southwest Pacific), where we collected two shallow- and two deep-water sponge species ( Tedania sp., Suberea meandrina , Farrea raoulensis , Artemisina sp.) for ex-situ incubation experiments to detect whether these sponges may process dissolved organic matter. We assessed the biochemical and phospholipid-derived fatty acids (PLFAs) and measured dissolved organic carbon (DOC) and total dissolved nitrogen (TDN) fluxes. Changes in fluorescent dissolved organic matter (FDOM) over time were analyzed and the results were linked to the bacterial communities of the sponge holobiont. Dried sponge tissue consisted of 17.5 ± 3.75% organic (org.) C and of 4.34 ± 1.02% total nitrogen (TN) with a natural stable isotope composition of -19.0 ±0.25‰ for δ13org. C and of 10.2 ±2.43‰ for δ15TN. None of the DOC fluxes was significant and only the release of TDN by Tedania sp. was significantly different from 0 μmol TDN g org. C-1 d-1. We detected the presence of four fluorophores in the FDOM pool: 2 tryptophan- and protein-like fluorophores (C1, C2), 1 humic-like fluorophore (C3), and 1 tyrosine-like fluorophore (C4). The maximum fluorescence intensity Fmax of C1 decreased significantly in S. meandrina incubations, whereas Fmax of C2 grew in the same incubations. Fmax of C3 increased in Tedania sp. incubations, in which Fmax of C4 decreased. In comparison, Fmax of C4 in S. meandrina rose. The PLFA composition of sponge tissue was dominated by long-chain fatty acids, saturated fatty acids, and monosaturated fatty acids and most PLFAs were sponge- and bacteria-specific. The bacterial community of the demosponges Artemisina sp., S. meandrina and Tedania sp. consisted mostly of Proteobacteria and Chloroflexota, whereas the dominating bacteria phylum of the hexactinellid F. raoulensis was Proteobacteria. We proposed that the holobionts of S. meandrina and Tedania sp. contain bacteria that are involved in the transformation and degradation of DOM. In S. meandrina , Chloroflexota and Poribacteria may degrade tryptophan-like fluorophores to a chemically modified tryptophan-like and protein-like fluorophore, while producing a tyrosine-like fluorophore. In Tedania sp., Chloroflexota may contribute to the release of significant amounts of TDN by producing humic-like fluorophores, while degrading tyrosine-like fluorophores. Farrea raoulensis may not take up DOM due to a lack of Poribacteria and Chloroflexota or may use colloidal instead of truly dissolved DOC. ### Competing Interest Statement The authors have declared no competing interest.

Spectroscopy-guided isolation of extracts of the Tongan marine sponge Hyattella cf. intestinalis (Lamarck, 1814) has resulted in the reisolation of the labdane diterpenoid luakuliide A (1) and one new congener, luakulialactam A (2). In addition to establishing the absolute configuration of 1, synthetic modifications to the luakuliide framework at key positions has created a set of six derivatives (3-8) which were used to interrogate a structure-activity relationship relating to the immunomodulatory effects of luakuliide A. This revealed that compounds 4, 5, and 6, bearing substituted furan motifs, show potent activity in primary macrophages by inhibiting pro-inflammatory cytokine production, while upregulating cellular metabolism and anti-inflammatory IL-10 production at nanomolar concentrations. This is an activity profile consistent with macrophages modulated toward an anti-inflammatory phenotype associated with wound-healing and resolution of inflammation.

The waters of Aotearoa New Zealand span over 4.2 million km2 of the South Pacific Ocean and harbour a rich diversity of seafloor-associated taxa. Due to the immensity and remoteness of the area, there are significant gaps in the availability of data that can be used to quantify and map the distribution of seafloor and demersal biodiversity, limiting effective management. In this study, we describe the development and accessibility of an online atlas of seabed biodiversity that aims to fill these gaps. Species distribution models were developed for 579 taxa across four taxonomic groups: demersal fish, reef fish, subtidal invertebrates and macroalgae. Spatial layers for taxa distribution based on habitat suitability were statistically validated and then, as a further check, evaluated by taxonomic experts to provide measures of confidence to guide the future use of these layers. Spatially explicit uncertainty (SD) layers were also developed for each taxon distribution. We generated layer-specific metadata, including statistical and expert evaluation scores, which were uploaded alongside the accompanying spatial layers to the open access database Zenodo. This database provides the most comprehensive source of information on the distribution of seafloor taxa for Aotearoa New Zealand and is thus a valuable resource for managers, researchers and the public that will guide the management and conservation of seafloor communities. The atlas of seabed biodiversity for Aotearoa New Zealand is freely accessible via the open-access database Zenodo under https://doi.org/10.5281/zenodo.7083642 (Stephenson et al., 2022).

Clostridioides difficile infection (CDI) is a leading cause of antibiotic-associated diarrhoea across the globe. Although treatable with a restricted number of antibiotics, the emergence of resistant variants and high relapse rates necessitate alternative countermeasures. Phage therapy represents an attractive option. However, its implementation is handicapped by the narrow host specificity of the C. difficile bacteriophages isolated to date. One strategy to rationally expand phage host range would be to make appropriate modifications to the phage receptor binding protein (RBP). Here, we identify the tail fibre as the RBP of two Myoviridae phages, ΦCD1801 and ΦCD2301, which were previously isolated and propagated using the C. difficile strains CD1801 (RT078) and CD2301 (RT014), respectively. Contrary to studies into reprogramming the host ranges of phage of other bacterial other species, exchanging the tail fibre genes ( tcf/tfp ) alone between the two phage was insufficient to change host specificity. Rather, alterations to host range were dependent their exchange together with a putative chaperone encoded by hyp , localised adjacent to the tail fibre gene. Capitalising on this discovery, CRISPR/Cas9 was used to change the host range of one phage to that of the other by swapping the respective tcf/tfp and hyp genes. Significantly, one of the resulting mutants, surpassed both parental phages in terms of host range and efficiency of infection. This is the first time that genome engineering has successfully expanded the host range of a C. difficile phage, a prerequisite for implementing phage for the treatment of CDI. Importance Alternatives to antibiotics for treating Clostridioides difficile infection (CDI) are urgently required. Phage therapy presents an attractive option as it has the potential to clear the infection with minimal microbiome disruption and eliminate the possibility of recurrence. However, the C. difficile bacteriophages isolated to date have highly restricted host ranges. Moreover, rational strategies to alter specificity have till now been precluded as the identity of the phage receptor binding proteins involved was largely unknown. Here, we demonstrated that tail fibre proteins and an associated putative chaperone determine the host range of two Myoviridae phage. This enabled the alteration of specificity through CRISPR-mediated genome editing and the creation of a phage derivative with a host range and infection efficiency exceeding that of the parental phages. This is the first time that the host range of a C. difficile phage has been successfully expanded through rational genome engineering.

Historically, sponge classification is based on the interpretation of morphological characters, whose phylogenetic information content is frequently limited, subject to homoplasies, or prone to environmental plasticity (e.g., Chombard et al. 1998). Therefore, the currently accepted order-level classification of its largest class, Demospongiae, has been largely revised with molecular phylogenetic data (Morrow & Cárdenas 2015). Nevertheless, numerous sponge genera with ambiguous or provisoric phylogenetic placement still await definite classification.

In the present study, we describe two new species of Corallistidae from Brazil, comparing them to all valid species of the respective genera. Both are notable Porifera records, with the first specimen of Neophrissospongia Pisera and Lévi, 2002 registered for the Brazilian coast and the first specimen of Awhiowhio Kelly, 2007 registered for the Atlantic Ocean. The specimens were preserved in 80% ethanol and analyzed following classical procedure for Demospongiae, with dissociated spicule mounts, skeletal sections and Scanning Electron Microscopy. Neophrissospongia jorgeorum sp. nov. is differentiated from its congeners by the categories of spicules present, especially the lack of streptasters/amphiasters. Awhiowhio saci sp. nov. is characterized especially by the presence of spiraster-shaped microrhabds and microxeas.

Generating spatial predictionsThe spatial distribution for each taxon was estimated using ensemble SDMs that were generated using the combined outputs from flexible machine learning Boosted Regression Tree (BRT) and Random Forest (RF) models.In subsequent sections we describe the biological data (from four biotic groups: demersal fish, reef fish, subtidal invertebrates and macroalgae), the spatially explicit environmental data, and how these were combined to predict the taxa distributions used in the atlas of seabed biodiversity of Aotearoa New Zealand. Biological samples Demersal fishFish species records (n = 391,198) (including information on research cruise identifier, gear type, date, minimum and maximum depth of trawl, and GPS location) from 1979 -2016 were extracted from the research trawl database 'TRAWL' (Niwa, 2014(Niwa, , 2018)).The data were groomed to only keep those records identified to species level, collected using bottom trawls and within the Aotearoa New Zealand Exclusive Economic Zone (EEZ) and Territorial Sea (TS).To minimise the effect of spatial bias in the occurrence data, species records were aggregated spatially to a 1 km grid resolution (Stephenson et al., 2020).Because of difficulties in correcting for differences in trawl methods, all catch records were converted into presence (Lundquist et al., 2020).To ensure distribution models were robust, only demersal fish species with ≥ 50 unique spatial locations were retained for analysis.The final dataset included presence/absence records of 235 demersal fish taxa at 28,599 unique sampling locations. Reef FishThe relative abundance of reef fishes were obtained from 467 SCUBA dives made around the coast of Aotearoa New Zealand over an 18-year period from November 1986 to December 2004 (for detailed methodology see Smith et al. (2013)).The data were groomed for a previous study by Smith et al. (2013) and all records were provided to species level identification.Species records were aggregated (to presence/absence) spatially to a 250 m grid resolution and included observations of 160 species at 339 unique sampling locations.To ensure distribution models were robust, only reef fish species with ≥ 35 unique spatial locations were retained for analysis.The final dataset included presence/absence records of 51 reef fish taxa at 429 unique sampling locations. Subtidal InvertebratesSubtidal invertebrate occurrence records (n = 127,330) (including GPS location, species name, collection date, and sampling gear used) from 1896 -2019 were extracted from TRAWL (n = 56,841), NIWA invert (n = 59,144), Te Papa (n = 2943) and Auckland Museum (n = 8402) databases.Only those records that had been classified to at least genus level and included information on sampling gear were extracted.Each record included information on the date, GPS location, survey and collection method.Across the four databases, 208 different methods were used to sample subtidal invertebrates, although many of these were name variants of commonly used sampling gears.To account for both the large number of gear types recorded and the differences in sampling parameters, gear types were grouped into catchability categories (Table S1).Catchability was assumed to be influenced by gear size, deployment area and selectivity (Stephenson et al., 2018b).Following categorisation of gear types, four gear classes were retained for species distribution modelling: SMG (small size, medium deployment area, general selectivity), SSG (small size, small deployment area, general selectivity), MMG (medium size, medium deployment

Seamounts on subantarctic New Zealand's Macquarie Ridge, including parts of Australia's Exclusive Economic Zone surrounding Macquarie Island, have been demonstrated to be a rich source of new species of carnivorous sponges (Demospongiae Sollas, Poecilosclerida Topsent, Cladorhizidae Dendy). Four new species of Abyssocladia Lévi, 1964, are described from Macquarie Ridge seamounts and at other disparate locations: Abyssocladia lanceola sp. nov. from Seamounts 7, 8, and 9 (Australia EEZ), Seamount 10 (International Waters), and the South Tasman Rise; Abyssocladia rowdeni sp. nov., first collected from diffuse hydrothermal vent sites at Brothers Seamount on the Southern Kermadec Ridge and recorded here from the non-venting seamounts on Chatham Rise to the east of the South Island of New Zealand; Abyssocladia tumulorum sp. nov., found exclusively on the Chatham Rise; and Abyssocladia sonnae sp. nov. from Monowai Seamount on the Tonga-Kermadec Ridge in International Waters, also found, surprisingly, on Macquarie Ridge's Seamount 8 (Australia EEZ). Patriciacladia gen. nov. has been established for a new species of Cladorhizidae discovered on Macquarie Ridge and Chatham Rise. Patriciacladia enigmatica gen. et sp. nov. is highly unusual in that it possesses palmate isochelae not typically found in Cladorhizidae and has a long branch in phylogenetic analysis of the family, supporting the establishment of a new genus and species for Abyssocladia n. sp. B (QM G339872, was NIWA 41033): 28S rDNA: LN870583, COI: LN870445, Macquarie Ridge) in Hestetun et al. (2016a: table 1; 2017: fig. 15). The discovery of two new species, again from the Macquarie Ridge and other New Zealand locations, expands support for the establishment of a new genus, Australocladia gen. nov., which contains several additional species nested as a monophyletic clade within the large, heterogenous, and paraphyletic Abyssocladia clade in molecular phylogenetic analyses. Australocladia sphaerichela gen. et sp. nov. and Au. alopecura gen. et sp. nov. both possess spherical abyssochelae, funnel-shaped expansions which may contain spermatophores on the body, substrongyles in the attachment base, and a generally southern hemisphere distribution.

Glass sponges (Hexactinellida) constitute important parts of ecosystems on the deep-sea floor worldwide. However, they are still an understudied group in terms of their diversity and systematics. Here, we report on new specimens collected during RV Sonne expedition SO254 to the New Zealand region, which has recently emerged as a biodiversity hotspot for hexactinellids. Examination of the material revealed several species new to science or so far unknown from this area. While formal taxonomic descriptions of a fraction of these were published earlier, we here briefly report on the morphology of the remaining new species and use the collection to greatly expand the molecular phylogeny of the group as established with ribosomal DNA and cytochrome oxidase subunit I markers. In addition, we provide a chemical fingerprinting analysis on a subset of the specimens to investigate if the metabolome of glass sponges contains phylogenetic signal that could be used to supplement morphological and DNA-based approaches.

Clostridioides difficile is an opportunistic gut pathogen which causes severe colitis, leading to significant morbidity and mortality due to its toxins, TcdA and TcdB. Two intra-muscular toxoid vaccines entered Phase III trials and strongly induced toxin-neutralising antibodies systemically but failed to provide local protection in the colon from primary C. difficile infection (CDI). Alternatively, by immunising orally, the ileum (main immune inductive site) can be directly targeted to confer protection in the large intestine. The gut commensal, non-toxigenic C. difficile (NTCD) was previously tested in animal models as an oral vaccine for natural delivery of an engineered toxin chimera to the small intestine and successfully induced toxin-neutralising antibodies. We investigated whether NTCD could be further exploited to induce antibodies that block the adherence of C. difficile to epithelial cells to target the first stage of pathogenesis. In NTCD strain T7, the colonisation factor, CD0873, and a domain of TcdB were overexpressed. Following oral immunisation of hamsters with spores of recombinant strain, T7-0873 or T7-TcdB, intestinal and systemic responses were investigated. Vaccination with T7-0873 successfully induced intestinal antibodies that significantly reduced adhesion of toxigenic C. difficile to Caco-2 cells, and these responses were mirrored in sera. Additional engineering of NTCD is now warranted to further develop this vaccine.

Spatial datasets and associated metadata to support the publication of 'An atlas of seabed biodiversity for Aotearoa New Zealand'. The atlas contains prediction of spatial distribution, with associated uncertainty, of over 600 seafloor associated taxa throughout New Zealand waters and were developed using species distribution modelling approaches. Metadata containing model evaluation, expert appraisal scores and ancillary information for all spatial layers in the 'An atlas of seabed biodiversity for Aotearoa New Zealand' is also provided. A manuscript, accompanying the publication of the atlas, has been submitted under the same title. The abstract for the manuscript is as follows. The waters of Aotearoa New Zealand span over 4.2 million km2 of the South Pacific Ocean and harbour a rich diversity of seafloor associated taxa. Due to the immensity and remoteness of the area, there are significant gaps in the availability of data to quantify and map the distribution of seafloor and demersal biodiversity, limiting effective management. In this study, we describe the development and accessibility of an online atlas of seabed biodiversity that aims to fill these gaps. Species distribution models were developed for 579 taxa across four taxonomic groups: demersal fish, reef fish, subtidal invertebrates and macroalgae. Spatial layers for taxa distribution based on habitat suitability were statistically validated and then, as a further check, evaluated by taxonomic experts to provide measures of confidence to guide the future use of these layers. Spatially explicit uncertainty (SD) layers were also developed for each taxon distribution. We generated layer-specific metadata, including statistical and expert evaluation scores, which were uploaded alongside the accompanying spatial layers to an online open access marine data portal hosted by the New Zealand Department of Conservation. The online atlas is fully interactive, with search and plotting functions, and allows the export of single or multiple spatial layers on seafloor biodiversity. The atlas provides the most comprehensive database on the distribution of seafloor taxa for Aotearoa New Zealand and is thus an invaluable resource for managers, researchers and the general public that will guide the management and conservation of seafloor communities.

Family Latrunculiidae Topsent, 1922 comprises seven genera: Latrunculia Barboza du Bocage, 1869; Sceptrella Schmidt, 1870; Strongylodesma Lvi, 1969; Tsitsikamma Samaai Kelly, 2002; Cyclacanthia Samaai Kelly in Samaai et al. (2004); Bomba and Latrunclava Kelly, Reiswig Samaai in Kelly et al. (2016) (Samaai Kelly 2002; Kelly et al. 2016; Samaai et al. 2020), with 83 valid species predominantly in the Southern Hemisphere (de Voogd et al. 2021). Latrunculiidae are differentiated primarily on the form and ornamentation of the diagnostic discorhabd microscleres (see Fig. 1) which may be anisodiscorhabds (Latrunculia, Bomba), isospinodiscorhabds (Cyclacanthia), and isochiadiscorhabds (Tsitsikamma). These may be accompanied by an additional longer microsclere, the amphiclad sceptre and anisoconicorhabd, in Sceptrella and Latrunclava, respectively. Here we describe a new latrunculid genus and species, Biverticillus tenuissimus gen. et sp. nov., from Walters Shoal on the Madagascar Ridge south of Madagascar in the Western Indian Ocean (Fig. 1A), the diagnostic microscleres of which are anisospinodiscorhabds, with two centrally located equidiametral whorls, equally spaced between each other and the apical whorl and manubrium. The microscleres are aniso- in their form because the apical and basal substructures differ slightly in the angle of repose of the spines.

Marine sponges are exceptionally prolific sources of natural products for the discovery and development of new drugs. Until now, sponges have contributed around 30% of all natural metabolites isolated from the marine environment. Family Latrunculiidae Topsent, 1922 (class Demospongiae Sollas, 1885, order Poecilosclerida Topsent, 1928) is a small sponge family comprising seven genera. Latrunculid sponges are recognized as the major reservoirs of diverse types of pyrroloiminoquinone-type alkaloids, with a myriad of biological activities, in particular, cytotoxicity, fuelling their exploration for anticancer drug discovery. Almost 100 pyrroloiminoquinone alkaloids and their structurally related compounds have been reported from the family Latrunculiidae. The systematics of latrunculid sponges has had a complex history, however it is now well understood. The pyrroloiminoquinone alkaloids have provided important chemotaxonomic characters for this sponge family. Latrunculid sponges have been reported to contain other types of metabolites, such as peptides (callipeltins), norditerpenes and norsesterpenes (trunculins) and macrolides (latrunculins), however, the sponges containing latrunculins and trunculins have been transferred to other sponge families. This review highlights a comprehensive literature survey spanning from the first chemical investigation of a New Zealand Latrunculia sp. in 1986 until August 2020, focusing on the chemical diversity and biological activities of secondary metabolites reported from the family Latrunculiidae. The biosynthetic (microbial) origin and the taxonomic significance of pyrroloiminoquinone related alkaloids are also discussed.

New Zealand's surrounding deep waters have become known as a diversity hotspot for glass sponges (Porifera: Hexactinellida) in recent years, and description and collection efforts are continuing. Here we report on eight rossellids (Hexasterophora: Lyssacinosida: Rossellidae) collected during the 2017 RV Sonne cruise SO254 by ROV Kiel 6000 as part of Project PoribacNewZ of the University of Oldenburg, Germany. The material includes six species new to science, two of which are assigned to a so far undescribed genus; we further re-describe two previously known species. The known extant rossellid diversity from the New Zealand region is thus almost doubled, from nine species in five genera to 17 species in eight genera. The specimens described here are only a small fraction of hexactinellids collected on cruise SO254. Unfortunately, the first author passed away while working on this collection, only being able to complete the nine descriptions reported here. The paper concludes with an obituary to him, the world-leading expert on glass sponge taxonomy who will be greatly missed.