BORDAU 1, Restreint, MAINBAZA, MUSORSTOM 10, MUSORSTOM 3

We inventoried all nine species of the ‘Acanthephyra purpurea’ complex, one of the most abundant and cosmo­ politan group of mesopelagic shrimps. We used 119 specimens at hand and genetic data for 124 specimens from GenBank and BOLD. Phylogenetic analysis of four genes (COI, 16S, NaK, and enolase) showed that the ‘Acan­ thephyra purpurea’ complex is polyphyletic and encompasses two species groups, ‘A. purpurea’ (mostly Atlantic) and ‘A. smithi’ (Indo-West Pacific). The ‘A. purpurea’ species group consists of two major molecular clades A. pelagica and A. kingsleyi – A. purpurea - A. quadrispinosa. Molecular data suggest that hitherto accepted species A. acanthitelsonis, A. pelagica, and A. sica should be considered as synonyms. The Atlantic is inhabited by at least two cryptic genetic lineages of A. pelagica and A. quadrispinosa. Morphological analyses of qualitative and quantitative (900 measurements) characters resulted in a tabular key to species and in a finding of four evolutionary traits. Atlantic species showed various scenarios of diversification visible on mitochondrial gene level, nuclear gene level, and morphological level. We recorded and discussed similar phylogeographic trends in diversification and in distribution of genetic lineages within two different clades: A. pelagica and A. kingsleyi – A. purpurea - A. quadrispinosa.

ATIMO VATAE, MAINBAZA, MD28 (SAFARI II), MUSORSTOM 9, SALOMONBOA 3, Walters Shoal

A small collection of cephalopods collected from the waters off the Wallis and Futuna Islands in the central South Pacific s reported. The collection comprises 17 specimens belonging to 13 taxa in six families. Three forms of Heteroteuthis are present, representing at least two species, including what appears to be a new species which is not named because of the limited material available. A record of Idioteuthis cordiformis represents a considerable range extension. The new species Sepia subplana sp. Novo represents the eastern-most record of any cuttlefish in the Pacific Ocean.

MUSORSTOM 7

A new genus and species, Choneteuthis tongaensis gen. et sp. nov., is described from the waters around Tonga in the central South Pacific Ocean. The new genus does not clearly fit in any of the currently recognized subfamilies of the family Sepiolidae, justifying a reconsideration of the subfamilial subdivision of the family.

BORDAU 2

The first comprehensive phylogenetic study of the family Oplophoridae is based on four molecular markers and 87 morphological characters. We have examined and coded five major groups of morphological characters related to the rostrum (nine characters), the carapace (10), the abdomen and telson (34), the exopods (eight) and the armature of the posteriormost three pereopods (22). Abdomen/telson-linked characters are the most important in support of genus level and species-group level clades; abdomen/telson-linked, rostrum-linked characters and the armature of the last three pereopods explain the main bulk of speciation. Four robustly supported species groups within Systellaspis are designated: the S. debilis species group, the S. cristata species group, the S. braueri species group and the S. pellucida species group. We provide an amended key to all genera, species groups and species of Oplophoridae. We reveal three groups of morphological characters, which are likely coupled with the same locomotive function and thus evolved as a single unit: carapace, abdomen and exopods. We show that the armature of the posteriormost three pereopods evolved independently of other characters and suggest that this group is linked to such biological roles as mating and grooming.

Restreint, BIOPAPUA, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, MUSORSTOM 3, SALOMONBOA 3

Abstract The phylogenetic study of the deep-sea genus Bentheogennema is based on four molecular markers and 79 morphological characters. All four previously recognized species and two new species of Bentheogennema, representatives of all other genera and species groups of Benthesicymidae, and three outgroups were included in the analyses. We have examined and coded six major groups of morphological characters related to the carapace (three characters), the pleon and the telson (14), the mouthparts (nine), the armature of the pereopods (five), the thelycum (27) and the petasma (21). Results of morphological and molecular analyses were similar. Two species were transferred from Bentheogennema to other genera (for one of them a new genus was erected) and two new species of Bentheogennema were described. Three pelagic genera (Gennadas, Bentheogennema and a new genus) created a robust clade. The divergence of this clade is linked to ‘smoothening’ of the body (reduction of the branchiostegal spine on the carapace, reduction and loss of the dorsolateral spines and the end-piece on the telson) and elaboration of the copulatory structures. We provide amended diagnoses of these three pelagic genera and key to species of Bentheogennema.

Restreint, BENTHEDI, BIOGEOCAL, BIOPAPUA, HALIPRO 2, MD32 (REUNION)

Hymenodora represents the most scantily studied branch of the pelagic shrimp belonging to the superfamily Oplophoroidea. We present a phylogenetic revision based on 80 morphological characters and six genes. Molecular and morphological phylogenetic analyses, along with molecular distances calculated with the use of six genes, suggest a family-level status of the clade Hymenodoridae including Hymenodora and Sclerodora, which is also supported by morphological characters linked to the mouthparts. We erect and diagnose a new family and provide a key to families of Oplophoroidea. We tested seven morphological characters, found that only one of them provides a confident identification of Hymenodora gracilis and Hymenodora glacialis complexes. We provide an amended key to species of Hymenodoridae. Molecular trees, along with genetic distances based on COI and 16S genetic markers, showed that H. gracilis and H. glacialis represent complexes of cryptic lineages that cannot be identified on the basis of solitary morphological characters; however, when we included seven morphological characters and ran principal component analysis and generalized linear mixed models, we could distinguish all cryptic lineages confidently. Evolutionary traits of Hymenodoridae are linked to adaptations to feeding in the deep sea (mouthparts), strengthening the membranous carapace (carinae, sulci) and passive defence (shape and proportions of the rostrum and carapace).

ATIMO VATAE, BIOPAPUA, MAINBAZA, NORFOLK 2, Walters Shoal

Abstract The shrimp genera Ephyrina, Meningodora and Notostomus have an unusual carapace strengthened with carinae and a half-serrated mandible, which may suggest a possible monophyly of this group. Here we test this hypothesis and present the first phylogenetic study of these genera based on 95 morphological characters (all valid species coded) and six molecular markers (71% of valid species sequenced). Representatives of all genera of Oplophoridae (sister to Acanthephyridae) were outgroups, 32 species belonging to all genera and potentially different clades of Acanthephyridae were ingroups. Both morphological and molecular analyses retrieve trees with similar topology. Our results reject the hypothesis of a clade formed by Ephyrina + Meningodora + Notostomus. We show that Ephyrina and Notostomus are monophyletic, both on morphological and on molecular trees, Meningodora gains support only on morphological trees. Evolutionary traits in the Ephyrina and Meningodora + Notostomus clades are different. Synapomorphies are mostly linked to adaptations to forward motion in Ephyrina (oar-like meri and ischia of pereopods, stempost-like rostrum) and to progressive strengthening of the carapace and pleon in Meningodora and Notostomus (net of sharp carinae). Unusual mandibles evolved in the clades independently and represent convergent adaptations to feeding on gelatinous organisms.

ATIMO VATAE, Restreint, BIOPAPUA, Restreint, GUYANE 2014, KAVIENG 2014, MAINBAZA, MD20 (SAFARI), MIRIKY, MUSORSTOM 2, MUSORSTOM 3, PAPUA NIUGINI, SALOMONBOA 3, Walters Shoal

This revision of the scissurellid genus Satondella Bandel, 1998 is mainly based on shell characters due to the availability of only a few live collected specimens. There are seven Recent species (two described as new) and one Eocene fossil. Satondella minuta Bandel, 1998, the type species from Indonesia, is redescribed and its range extended to New Caledonia, Solomon and Fiji Islands. Satondella tabulata (Watson, 1886) is only known from type material off Culebra Island (Puerto Rico); lectotype and paralectotypes are here designated, and similar material from the Indo-Pacific is discussed. Satondella brasiliensis (Mattar, 1987) is another W. Atlantic species, ranging from Bermuda to Brazil. Satondella senni (Geiger, 2003) is only known from the E. Pacific (Easter Island) and Satondella danieli Segers, Swinnen & Abreu, 2009 from the NE. Atlantic Ocean (Desertas and Madeira Islands). The two new species are distributed through the E. Indian and W. Pacific oceans (S. cachoi n. sp.) and W. Pacific (S. dantarti n. sp.). The Tongan Eocene fossil S. kondoi (Ladd, 1970) is redescribed and illustrated with SEM images. Satondella brasiliensis and S. cachoi have a typical scissurellid radula, except for uniquely having one cusp on the inner edge of the third lateral. The monophyly of the genus is discussed, since species currently included in Satondella show two clearly different shell patterns but all share the unique chimney-like foramen.

BATHUS 2, BATHUS 3, BENTHEDI, BERYX 11, BIOCAL, BIOGEOCAL, BORDAU 1, CALSUB, EBISCO, MUSORSTOM 10, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, SMIB 3, SMIB 8

LIFOU 2000, MONTROUZIER

Six mid-depth octopuses of the Order Octopoda are reported from the Banda and Arafura Seas off Indonesia and northern Australia, based on material collected through the collaborative French-Indonesian KARuBAR cmise of 1991. Octopod material was collected through benthic trawls at 18 of 91 stations, at depths between 199 and 869 metres. Two new species are described here, Benthoctopus karubar sp. nov. and Octopus pyrum sp. nov. An additional species of the genus Octopus is reported as indeterminate but distinct from O. pyrum. The genus Pteroctopus is reported from IndoPacifie waters for the first time, based on female material collected through the KARuBAR cmise and linked with additional male material collected off New Caledonia and Vanuatu. Eledone palari is recorded as a northerly extension to the Australian distribution reported in the original description for this species. A single submature female of the pelagie octopod, Haliphron atlanticus (previously treated under the name Alloposus mollis), is also reported from the region. The depth distributions and phylogenetic affinities of this fauna are discussed.

KARUBAR

The distribution of dissolved iodine in seawater is sensitive to multiple biogeochemical cycles, including those of nitrogen and oxygen. The iodine-to-calcium ratio (I/Ca) of marine carbonates, such as bulk carbonate or foraminifera, has emerged as a potential proxy for changes in past seawater oxygenation. However, the utility of the I/Ca proxy in deep-sea corals, natural archives of seawater chemistry with wide spatial coverage and radiometric dating potential, remains unexplored. Here, we present the first I/Ca data obtained from modern deep-sea corals, specifically scleractinian and bamboo corals, collected from the Atlantic, Eastern Pacific, and Southern Oceans, encompassing a wide range of seawater oxygen concentrations (10–280 μmol/kg). In contrast to thermodynamic predictions, we observe higher I/Ca ratios in aragonitic corals (scleractinian) compared to calcitic corals (bamboo). This observation suggests a strong biological control during iodate incorporation into deep-sea coral skeletons. For the majority of scleractinian corals, I/Ca exhibits a covariation with local seawater iodate concentrations, which is closely related to seawater oxygen content. Scleractinian corals also exhibit notably lower I/Ca below a seawater oxygen threshold of approximately 160 μmol/kg. In contrast, no significant differences in I/Ca are found among bamboo corals across the range of oxygen concentrations encountered (15–240 μmol/kg). In the North Atlantic, several hydrographic factors, such as temperature and/or salinity, may additionally affect coral I/Ca. Our results highlight the potential of I/Ca ratios in deep-sea scleractinian corals to serve as an indicator of past seawater iodate concentrations, providing valuable insights into historical seawater oxygen levels.

MUSORSTOM 9

Partecosta milesi sp. nov. is described as new and compared to its sole morphological congener in the SW Indian Ocean. The South African members of the genus Gradaterebra are revised of which knowledge of the shell morphology remains only peripheral.

ATIMO VATAE

The deep sea is the largest biome on Earth and hosts the majority of as yet undescribed species; description of these may trigger a new mindset about evolution and function of characters. We describe and diagnose a new genus and species Sclerodora crosnieri sp. nov. belonging to the superfamily Oplophoroidea. We examined and coded 81 characters for morphological analyses and used four gene markers for molecular analyses involving the new taxon and representatives of all other genera of Oplophoroidea. Retrieved morphological and molecular trees were similar and suggested that the new genus is a sister group to Hymenodora and both form a clade sister to the rest of Acanthephyridae. We provide an amended key to all genera of Oplophoroidea. We found an unusual chelate structure on the dactyl of the fifth pereopod, tested and confirmed a hypothesis that this structure is common for the whole family Acanthephyridae. We suggest that this derived structure is linked to an active cleaning of branchia—a function associated with chelipeds in some other carid shrimps. Convergent chelate structures are likely efficient for cleaning branchia, whichever appendage is adapted for these functions. In Oplophoridae (sister to Acanthephyridae), cleaning function is carried out by well-developed epipods.

ATIMO VATAE, Restreint, Restreint, Restreint, Walters Shoal, caride 1

We describe and diagnose a new species of Acanthephyra (Acanthephyridae: Caridea: Decapoda) and provide an amended key to all species of the genus. In order to assess the taxonomic position of the new species, we examined and coded 55 characters in available specimens of Acanthephyra and ran morphological phylogenetic analyses. We also used a COI gene marker for molecular analyses of the new species and other available specimens of Acanthephyra. Both analyses retrieved an unexpected grouping of species that contradicted a recently accepted morphological grouping. We tested a new, quantitative, set of characters and found that three of them may explain the molecular grouping of the genus. These characters are linked to: (1) proportions of the 6th pleonic somite, (2) length of the same against carapace length, and (3) length of the same against length of two preceding somites. We suggest that these characters mirror evolutionary traits in Acanthephyra and discuss their possible adaptive sense.

Restreint, ATIMO VATAE, BENTHAUS, BIOPAPUA, GUYANE 2014, MAINBAZA, MD20 (SAFARI), MD28 (SAFARI II), MIRIKY, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 9, SALOMONBOA 3, Walters Shoal

Abstract A phylogenetic study of deep-sea dendrobranchiate genera Altelatipes, Benthesicymus and Benthonectes based on four molecular markers and 91 morphological characters is presented. All currently recognized species of these genera, representatives of all other genera and species groups of Benthesicymidae, and three outgroups were included in the analyses. The molecular and morphological methods retrieved similar results, the molecular methods provided better resolution of deeper nodes and higher clade support. Both types of analyses showed paraphyly of Benthesicymus, which encompass five robust clades, four of which are diagnosed as new genera (type species in parentheses): Benthesicymus s.s. (B. crenatus), Bathicaris gen. nov. (Benthesicymus brasiliensis), Dalicaris gen. nov. (Benthesicymus altus), Trichocaris gen. nov. (Benthesicymus bartletti) and Maorrancaris gen. nov. (Benthesicymus investigatoris). Altelatipes was found to be monophyletic. The evolution of the major clades of Benthesicymidae is shown to be linked to trophic specialization, while further divergence at the genus level is mainly related to sexual evolution seen in the elaboration of the copulatory structures. We provide amended diagnoses of the previously recognized and new genera, key to species of each of these genera and include an updated key to genera of Benthesicymidae.

Restreint, BENTHEDI, BIOCAL, BIOPAPUA, HALIPRO 2, KARUBENTHOS 2, MD32 (REUNION)

Benthesicymidae is a monophyletic group of Decapoda adapted to a life on the sea-floor, in the near-bottom layer, in the bathy- and in the mesopelagic, within an impressive depth range from a few hundred metres (Gennadas) to several thousand metres (Benthesicymus). Higher taxa are known to conquer all main oceanic biotopes such as the benthic, benthopelagic, and pelagic and a wide depth range but few family-level groups have clades evolved within all these oceanic realms. Therefore, the global fauna of Benthesicymidae provides a rare opportunity for an insight into phylogenetic processes favouring colonisation of all principal oceanic biotopes. The first comprehensive phylogenetic study of Benthesicymidae (all 37 valid species) is based on six molecular markers and 105 morphological characters (including 72 female and male copulatory characters). Analyses resulted in trees with similar topology and the same set of robust clades. Molecular methods based on 167 sequences (84 new) provided better resolution of deeper nodes and generally higher support of the clades, while morphological methods allowed analyses of all valid species of the global fauna. Phylogenetic analyses support the monophyly and robustness of all currently known genera except Gennadas, which was split into Gennadas Bate, 1881, Amalopenaeus Smith, 1882, and Notogennema gen. nov. We also retrieved two major clades for which we erected two new subfamilies: Benthesicyminae subfam. nov. (presumably benthic, genera Altelatipes, Bathicaris, Benthesicymus, and Benthonectes) and Gennadinae subfam. nov. (presumably pelagic, genera Amalopenaeus, Bentheogennema, Benthoecetes, Boreogennema, Gennadas, Maorrancaris, and Notogennema gen. nov.). We revealed two groups of morphological characters, that are interlinked evolutionarily: (1) petasma and thelycum; (2) body, mouthparts, and pereopods. Morphological traits within benthic and pelagic clades are different, a model explaining the differences is proposed. Along with previous studies, our results confirm the idea that the elaboration of the copulatory structures is a key to successful colonisation of the pelagic realm. These results extend our knowledge about evolution in the largest habitual biotope of our planet and phylogenetic processes favouring colonisation of all principal oceanic biotopes.

BENTHEDI, BIOCAL, BIOPAPUA, HALIPRO 2, KARUBENTHOS 2, MAINBAZA, MD32 (REUNION), MIRIKY, MUSORSTOM 8

Leptochela Stimpson (1860) is a shallow-water, benthopelagic genus within the predominantly pelagic superfamily Pasiphaeoidea. We inventoried a global fauna of 17 currently valid species of Leptochela and identified a newly discovered eighteenth species. Our analysis combined both morphological and molecular data, using 13 characters (including two multistate characters) and 5 gene markers, respectively. The results revealed incongruence between the molecular and morphological datasets. However, our phylogenetic conclusions were based on a consensus approach, integrating morphological, molecular, and total evidence trees, which revealed three robust clades. We discuss the evolutionary development of quantitative and qualitative morphological traits in Leptochela and explore the potential causes of the incongruence between morphological and molecular signals, particularly in the context of pelagic eucarids transitioning from pelagic to benthopelagic habitats. Additionally, we describe the new species from Madagascar and provide a key to all known species of Leptochela.

ATIMO VATAE, LAGON, MUSORSTOM 1

Restreint, ANT-XXIX_3, ATIMO VATAE, BATHUS 2, BATHUS 4, Restreint, Restreint, Restreint, BENTHAUS, Restreint, BIOCAL, Restreint, Restreint, Restreint, BIOGEOCAL, BIOMAGLO, BIOPAPUA, Restreint, CEAMARC-AA, CHALCAL 2, CONCALIS, CORINDON 2, Restreint, Restreint, Restreint, Restreint, EBISCO, EXBODI, HALIPRO 2, Restreint, KANACONO, KANADEEP, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MD42 (SIBEX), MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, Restreint, NORFOLK 2, NanHai 2014, Restreint, SALOMON 1, SALOMON 2, SALOMONBOA 3, SPANBIOS, TAIWAN 2000, Restreint, TARASOC, Restreint, Walters Shoal, ZhongSha 2015