105 ???count.stations.label???
MADEEP
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- Corbari Laure (Leg 1)
- Olu‐Le Roy Karine (Leg 1)
- Corbari Laure (Leg 2)
- Samadi Sarah (Leg 2)
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Sat Apr 05 00:00:00 UTC 2014 Madang (Papouasie-Nouvelle-Guinée)???msg.table.location.campaign.stop.label???
Fri May 09 00:00:00 UTC 2014 Madang (Papouasie-Nouvelle-Guinée)| ???msg.field.stage.label??? | ???msg.table.stage.startDate.label??? | ???msg.table.stage.endDate.label??? | ???msg.table.stage.departure.label??? | ???msg.table.stage.arrival.label??? | ???msg.table.stage.ship.label??? |
|---|---|---|---|---|---|
| Leg 1 | Sun Apr 06 00:00:00 UTC 2014 | Fri Apr 18 00:00:00 UTC 2014 | Madang | Madang | Alis |
| Leg 2 | Sun Apr 20 00:00:00 UTC 2014 | Thu May 08 00:00:00 UTC 2014 | Madang | Madang | Alis |
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Partenaires de la mission :
Tropical Deep Sea-Benthos, La Planète Revisitée, Muséum National d'Histoire naturelle, CNRS INEE, Institut de Systématique, Evolution et Biodiversité, University of Papua New Guinea, IFREMER
Remerciements dans les articles :
"The material was collected during the MADEEP expedition (PICORBARI Laure, Karine OLU , Sarah SAMADI, RV Alis, https://doi.org/10.17600/14004000) in Papua New Guinea, as part of the Tropical Deep Sea Benthos and La Planète Revisitée expedition programs. This expedition operated under the regulations then in force in the country in question.
???msg.campaign.menu.bibliographies??? (88) [+] [-]
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Anker A. 2017. A new deep-water species of Alpheopsis Coutière, 1897 from the Indo-West Pacific (Decapoda: Alpheidae). Zootaxa 4226(4): 571-580. DOI:10.11646/zootaxa.4226.4.7
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Bertrand J.A., Borsa P. & Chen W.J. 2017. Phylogeography of the sergeants Abudefduf sexfasciatus and A. vaigiensis reveals complex introgression patterns between two widespread and sympatric Indo-West Pacific reef fishes. Molecular Ecology 26(9): 2527-2542. DOI:10.1111/mec.14044
???msg.biblio.abstract.label??? [+] [-]On evolutionary timescales, sea level oscillations lead to recurrent spatio-temporal variation in species distribution and population connectivity. In this situation, applying classical concepts of biogeography is challenging yet necessary to understand the mechanisms underlying biodiversity in highly diverse marine ecosystems such as coral reefs. We aimed at studying the outcomes of such complex biogeographic dynamics on reproductive isolation by sampling populations across a wide spatial range of a species-rich fish genus: the sergeants (Pomacentridae: Abudefduf). We generated a mutlilocus data set that included ten morpho-species from 32 Indo-West Pacific localities. We observed a pattern of mito-nuclear discordance in two common and widely distributed species: Abudefduf sexfasciatus and Abudefduf vaigiensis. The results showed three regional sublineages (Indian Ocean, Coral Triangle region, western Pacific) in A. sexfasciatus (0.6–1.5% divergence at cytb). The other species, A. vaigiensis, is polyphyletic and consists of three distinct genetic lineages (A, B and C) (9% divergence at cytb) whose geographic ranges overlap. Although A. vaigiensis A and A. sexfasciatus were found to be distinct based on nuclear information, A. vaigiensis A was found to be nested within A. sexfasciatus in the mitochondrial gene tree. A. sexfasciatus from the Coral Triangle region and A. vaigiensis A were not differentiated from each other at the mitochondrial locus. We then used coalescent-based simulation to characterize a spatially widespread but weak gene flow between the two species. We showed that these fishes are good candidates to investigate the evolutionary complexity of the discrepancies between phenotypic and genetic similarity in closely related species.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Campbell M.A., Chanet B., Chen J., Lee M. & Chen W. 2019. Origins and relationships of the Pleuronectoidei: Molecular and morphological analysis of living and fossil taxa. Zoologica Scripta 48(5): 640-656. DOI:10.1111/zsc.12372
???msg.biblio.abstract.label??? [+] [-]Flatfishes (Pleuronectiformes) are a species‐rich and distinct group of fishes characterized by cranial asymmetry. Flatfishes occupy a wide diversity of habitats, including the tropical deep‐sea and freshwaters, and often are small‐bodied fishes. Most scientific effort, however, has been focused on large‐bodied temperate marine species important in fisheries. Phylogenetic study of flatfishes has also long been limited in scope and focused on the placement and monophyly of flatfishes. As a result, several questions in systematic biology have persisted that molecular phylogenetic study can answer. We examine the Pleuronectoidei, the largest suborder of Pleuronectiformes with >99% of species diversity of the order, in detail with a multilocus nuclear and mitochondrial data set of 57 pleuronectoids from 13 families covering a wide range of habitats. We combine the molecular data with a morphological matrix to construct a total evidence phylogeny that places fossil flatfishes among extant lineages. Utilizing a time‐calibrated phylogeny, we examine the timing of diversification, area of origin and ancestral temperature preference of Pleuronectoidei. We find polyphyly or paraphyly of two flatfish families, the Paralichthyidae and the Rhombosoleidae, and support the creation of two additional families—Cyclopsettidae and Oncopteridae—to resolve their non‐monophyletic status. Our findings also support the distinctiveness of Paralichthodidae and refine the placement of that lineage. Despite a core fossil record in Europe, the observed recent diversity of pleuronectoids in the Indo‐West Pacific is most likely a result of the Indo‐West Pacific being the area of origin for pleuronectoids and the ancestral temperature preference of flatfishes is most likely tropical.
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Castro P. 2020. Brachyuran crabs (Crustacea: Brachyura) of eleven families of Dorippoidea, Goneplacoidea, Homoloidea, Palicoidea, Pilumnoidea, and Trapezioidea from Papua New Guinea, Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:141-206, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]Collection of 81 species belonging to 11 families of six superfamilies of brachyuran crabs are reported from expeditions in Papua New Guinea (BIOPAPUA (2010), PAPUA NIUGINI (2012), MADEEP (2014), and KAVIENG 2014 (2014) cruises). The species, belonging to Dorippoidea (Ethusidae), Goneplacoidea (Goneplacidae, Euryplacidae, Progeryonidae), Homoloidea (Latreilliidae), Palicoidea (Crossotonotidae, Palicidae), Pilumnoidea (Pilumnidae Eumedoninae) and Trapezioidea (Domeciidae, Tetraliidae, Trapeziidae) were mostly collected from deep water and are rarely collected and studied. Fifty species are recorded from the island of New Guinea for the first time. Ethusina ocellata Castro, 2005 (Ethusidae) was found to be a junior subjective synonym of Ethusina microspina Chen, 2000, and Ethusa crassipodia Castro, 2005 (Ethusidae) of Ethusa curvipes Chen, 1993. Ethusina exophthalma Castro, 2005 is reassigned to Ethusa Smith, 1884, as Ethusa exophthalma (Castro, 2005) n. comb. The females of Parethusa hylophora Castro, 2005 (Ethusidae) and Thyraplax digitodentata Castro, 2007 (Goneplacidae), respectively, are described for the first time. A neotype is designated for Trapezia rubridactyla Garth, 1971 (Trapeziidae). Color photographs of fresh material of many of the species are published for the first time.
???msg.biblio.biblioSurvey.label??? (21) [+] [-]AURORA 2007, BATHUS 3, BIOPAPUA, BOA1, EXBODI, HALIPRO 1, KARUBAR, KAVIENG 2014, MADEEP, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 8, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, TARASOC, TERRASSES
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Cervantes-Guerra Y.M. 2019. The deep sea tailings placement (DSTP) as alternative for the residuals management in the mining industry. 35: 18
???msg.biblio.abstract.label??? [+] [-]The article aims to clarify how the deep sea tailings depositions have been used worldwide as alternative mining practice. The paper is a checking of case studies where this technology is used. The available information sources were consulted, which included: case reports, scientific papers, theses and reports by proper authorities. It is achieved to expose the fundamental principles of operation and environmental impact of this technology in the marine environment by applying empirical methods and theoretical research, as well as an assessment of main cases in the world.
???msg.biblio.biblioSurvey.label??? (1) [+] [-] -
Corbari L., Frutos I. & Sorbe J.C. 2019. Dorotea gen. nov., a new bathyal genus (Amphipoda, Eusiridae) from the Solomon Sea (Papua New Guinea). Zootaxa 4568(1): 69. DOI:10.11646/zootaxa.4568.1.4
???msg.biblio.abstract.label??? [+] [-]A new species ascribed to a new genus of Eusiridae, Dorotea papuana gen. nov., sp. nov. is described from bathyal bottoms of the Solomon Sea (Papua New Guinea). Closely related to the genus Cleonardo, this new genus can be distinguished from most other known eusirid genera by the presence of a telson distally cleft and distinctly bilobate, of a distal spiniform process on uropod 1 peduncle and of a simple, stout and medium length dactylus on pereopods 5–7. The combination of all these characters can be considered relevant for the affiliation of this species to a new genus within Eusiridae. Due to its very close morphological affinity to Dorotea gen. nov., the bathyal sub-Antarctic species Eusiroides aberrantis Bellan-Santini & Ledoyer, 1987 cannot be maintained in the family Pontogeneiidae and it should be transferred to the family Eusiridae.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Dijkstra H.H. & Maestrati P. 2017. New species and new records of littoral and bathyal living Pectinoidea (Bivalvia: Propeamussiidae, Cyclochlamydidae, Pectinidae) from the western and southwestern Pacific. Zoosystema 39(4): 473-485. DOI:10.5252/z2017n4a3
???msg.biblio.biblioSurvey.label??? (13) [+] [-]BIOCAL, BIOPAPUA, BORDAU 1, DongSha 2014, GEMINI, KARUBAR, KAVIENG 2014, MADEEP, MUSORSTOM 5, NanHai 2014, PAPUA NIUGINI, TAIWAN 2013, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fassio G., Russini V., Buge B., Schiaparelli S., Modica M.V., Bouchet P. & Oliverio M. 2020. High cryptic diversity in the kleptoparasitic genus Hyalorisia Dall, 1889 (Littorinimorpha: Capulidae) with the description of nine new species from the Indo-West Pacific. Journal of Molluscan Studies 86(4): 401-421. DOI:10.1093/mollus/eyaa028
???msg.biblio.abstract.label??? [+] [-]Species in the family Capulidae (Littorinimorpha: Capuloidea) display a wide range of shell morphologies. Several species are known to live in association with other benthic invertebrates—mostly bivalves and sabellid worms, but also other gastropods—and are believed to be kleptoparasitic filter feeders that take advantage of the water current produced by the host. This peculiar trophic ecology, implying a sedentary lifestyle, has resulted in highly convergent shell forms. This is particularly true for the genus Hyalorisia Dall, 1889, which occurs in deep water in the Caribbean and Indo-West Pacific provinces, with two nominal species recognized so far. Combining morphological, ecological and molecular data, we assessed the diversity of the genus, its phylogenetic position inside the family and its association with its bivalve host, the genus Propeamussium de Gregorio, 1884 (Pectinoidea), resulting in the description of nine new cryptic species. When sympatric, species of Hyalorisia are associated with different host species, but the same species of Propeamussium may be the host of several allopatric species of Hyalorisia.
???msg.biblio.biblioSurvey.label??? (17) [+] [-]AURORA 2007, CONCALIS, CORSICABENTHOS 1, EBISCO, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.3, MADEEP, MAINBAZA, MIRIKY, NanHai 2014, PANGLAO 2004, PANGLAO 2005, SALOMON 2, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fassio G., Stefani M., Russini V., Buge B., Bouchet P., Treneman N., Malaquias M.A.E., Schiaparelli S., Modica M.V. & Oliverio M. 2022. Neither slugs nor snails: a molecular reappraisal of the gastropod family Velutinidae. Zoological Journal of the Linnean Society 197(4): 924-964. DOI:10.1093/zoolinnean/zlac091
???msg.biblio.abstract.label??? [+] [-]Abstract The systematics of the marine mollusc family Velutinidae has long been neglected by taxonomists, mainly because their often internal and fragile shells offer no morphological characters. Velutinids are usually undersampled owing to their cryptic mantle coloration on the solitary, social or colonial ascidians on which they feed and lay eggs. In this study, we address the worldwide diversity and phylogeny of Velutinidae based on the largest molecular dataset (313 specimens) to date, accounting for > 50% of the currently accepted genera, coupled with morphological and ecological data. Velutinids emerge as a diverse group, encompassing four independent subfamily-level lineages, two of which are newly described herein: Marseniopsinae subfam. nov. and Hainotinae subfam. nov. High diversity was found at genus and species levels, with two newly described genera (Variolipallium gen. nov. and Pacifica gen. nov.) and ≥ 86 species in the assayed dataset, 58 of which are new to science (67%). Velutinidae show a remarkable morphological plasticity in shell morphology, mantle extension and chromatic patterns. This variability is likely to be the result of different selective forces, including habitat, depth and trophic interactions.
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, BIOMAGLO, BIOPAPUA, CEAMARC-AA, CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, GUYANE 2014, ILES DU SALUT, KANACONO, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, PANGLAO 2004, PAPUA NIUGINI, SAKIZAYA 2019, SANTO 2006, Tuhaa Pae 2013, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A., Puillandre N., Herrmann M., Kantor Y., Oliverio M., Dgebuadze P., Modica M.V. & Bouchet P. 2018. The collapse of Mitra: molecular systematics and morphology of the Mitridae (Gastropoda: Neogastropoda). Zoological Journal of the Linnean Society 20: 1-85. DOI:10.1093/zoolinnean/zlx073/4855867
???msg.biblio.abstract.label??? [+] [-]Alongside confirmation of the monophyly of the gastropod family Mitridae, a recent molecular phylogenetic analysis disclosed multiple inconsistencies with the existing taxonomic framework. In the present study, we expanded the molecular sampling to 103 species, representing 26% of the 402 extant species currently accepted in the family and 16 of the 19 currently accepted extant genera; 83 species were sequenced for four molecular markers [cytochrome c oxidase subunit I (COI), 16S and 12S rRNA, and H3 (Histone 3)]. Molecular analyses were supplemented by morphological studies, focused on characters of the radula and, in a more restricted data set, proboscis anatomy. These data form the basis for a revised classification of the Mitridae. A first dichotomy divides mitrids into two unequal clades, Charitodoron and the Mitridae s.s. Species of Charitodoron show profound differences to all other Mitridae in foregut anatomy (lacking an epiproboscis) and shell morphology (smooth columella, bulbous protoconch of non-planktotrophic type), which leads to the erection of the separate family Charitodoronidae fam. nov. Three traditional subfamilies (Mitrinae, Cylindromitrinae and Imbricariinae) correspond to three of the inferred phylogenetic lineages of Mitridae s.s.; we redefine their contents, reinstate Strigatellinae Troschel, 1869 as valid and establish the new subfamily Isarinae. In the absence of molecular material, a sixth subfamily, Pleioptygmatinae, is included in Mitridae based on morphological considerations only. To resolve the polyphyly of Mitra and Cancilla in their current taxonomic extension, we reinstate the genera Episcomitra Monterosato, 1917, Isara H. & A. Adams, 1853 and Probata Sarasúa, 1989 and establish 11 new genera: Quasimitra, Roseomitra, Fusidomiporta, Profundimitra, Cancillopsis, Pseudonebularia, Gemmulimitra and Neotiara in Mitrinae; Imbricariopsis in Imbricariinae; Carinomitra and Condylomitra are left unassigned to a subfamily. Altogether 32 genera are recognized within the family. Their diversity and distribution are discussed, along with general trends in morphological evolution of the family.
???msg.biblio.biblioSurvey.label??? (26) [+] [-]ATIMO VATAE, AURORA 2007, BIOCAL, BIOPAPUA, BOA1, CONCALIS, CORAIL 2, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, SMIB 4, TARASOC, Tuhaa Pae 2013, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A., Ratti C., Kantor Y. & Puillandre N. 2025. THE CONASPRELLA ORBIGNYI (GASTROPODA: CONIDAE) COMPLEX REVISITED: NEW SPECIES REVEALED BY INCREASED SAMPLING.
???msg.biblio.abstract.label??? [+] [-]The genus Conasprella Thiele, 1929 is the second largest in the family Conidae. It encompasses 161 described species that mainly occur at bathyal depths. Despite this relatively high species diversity, species delimitation and taxonomy of the genus have barely been addressed with molecular data. In the present study, we revisit species delimitation in the Indo-Pacific Conasprella orbignyi complex based on data from a previous study and substantial original data. Integrative taxonomy applied to a dataset comprising 82 specimens revealed ten putative species, and available names were assigned to seven of them. Two unnamed species are new and described here as Conasprella zinaidae Fedosov & Puillandre, n. sp. (represented by a single sequenced specimen from Papua New Guinea) and Conasprella emilieae Puillandre & Fedosov, n. sp. (represented by four sequenced specimens, all from Papua New Guinea). Some populations within the Conasprella orbignyi complex show weak genetic structure but unusually high morphological variation, which overlaps differences among genetically distinct species. This variation renders identification of both new species on conchological grounds problematic. Therefore, we provide DNA-based diagnoses for both new species to facilitate their identification in future studies.
???msg.biblio.biblioSurvey.label??? (18) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, BOA1, EBISCO, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A.E., Caballer Gutierrez M., Buge B., Sorokin P.V., Puillandre N. & Bouchet P. 2019. Mapping the missing branch on the neogastropod tree of life: molecular phylogeny of marginelliform gastropods. Journal of Molluscan Studies 85(4): 439-451. DOI:10.1093/mollus/eyz028
???msg.biblio.abstract.label??? [+] [-]Marginelliform gastropods are a heterogeneous and diverse group of molluscs encompassing over 1,600 living species, among which are the smallest known neogastropods. The relationships of marginelliform gastropods within the order Neogastropoda are controversial, and the monophyly of the two marginelliform families the Marginellidae J. Fleming, 1828 and the Cystiscidae Stimpson, 1865, remains unconfirmed. DNA sequence data have never been used to assess the relationships of the marginelliform gastropods, making this group the only major branch missing in our current understanding of the neogastropod tree of life. Here we report results of the first multilocus phylogenetic analysis of marginelliform gastropods, which is based on a dataset comprising 63 species (20 genera) of Marginellidae and Cystiscidae, and a wide range of neogastropod lineages. The Marginellidae and Cystiscidae form a moderately supported clade that is sister to the family Volutidae. Marginellona gigas appears to be sister to all other marginelliforms. The subfamily Marginellinae was recovered as a well-supported clade, and good resolution of this part of the tree makes it possible to propose amendments to the family-level classification of the group. The relationship between Granulina and other marginelliforms could not be resolved and requires further study. Due to poor resolution of basal relationships within the Marginellidae–Cystiscidae clade, the monophyly of the Cystiscidae was neither confirmed nor convincingly rejected. The shell morphology of most marginellid and cystiscid genera is taxonomically not very informative but, nevertheless, of the traditionally recognized genera only Gibberula and Dentimargo were shown to be polyphyletic. Although a comprehensive systematic revision of the group requires more extensive taxonomic sampling (e.g. with better representation of the type species of nominal genus-group names), our results support the superfamily Volutoidea, comprising four families (Volutidae, Cystiscidae, Marginellidae and Marginellonidae), with the placement of the Granulinidae uncertain for the time being.
???msg.biblio.biblioSurvey.label??? (15) [+] [-]ATIMO VATAE, ???msg.security.private???, DongSha 2014, EXBODI, GUYANE 2014, ILES DU SALUT, INHACA 2011, KANACONO, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MADIBENTHOS, MAINBAZA, PAPUA NIUGINI, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A.E., Malcolm G., Terryn Y., Gorson J., Modica M.V., Holford M. & Puillandre N. 2019. Phylogenetic classification of the family Terebridae (Neogastropoda: Conoidea). Journal of Molluscan Studies 85(4): 359-388. DOI:10.1093/mollus/eyz004
???msg.biblio.abstract.label??? [+] [-]The conoidean family Terebridae is an intriguing lineage of marine gastropods, which are of considerable interest due to their varied anatomy and complex venoms. Terebrids are abundant, easily recognizable and widely distributed in tropical and subtropical waters, but our findings have demonstrated that their systematics requires revision. Here we elaborate the classification of Terebridae based on a recently published molecular phylogeny of 154 species, plus characters of the shell and anterior alimentary system. The 407 living species of the family, including seven species described herein, are assigned to three subfamilies: Pellifroniinae new subfamily, Pervicaciinae and Terebrinae. The Pellifroniinae comprises five deep-water species in two genera, Pellifronia and Bathyterebra n. gen. Pellifroniinae possess a radula of duplex marginal teeth, well-developed proboscis and venom gland, and a very small rhynchodeal introvert. The Pervicaciinae includes c. 50 species in the predominantly Indo-Pacific genera Duplicaria and Partecosta. Pervicaciinae possess salivary glands, a radula of solid recurved marginal teeth and a weakly developed rhynchodeal introvert, but lack proboscis and venom gland. The remaining Terebridae species are classified into 15 genera in the subfamily Terebrinae (including four genera described herein); nine genera are defined on the basis of phylogenetic data and six solely on shell morphology. The Indo-Pacific genera Profunditerebra n. gen., Maculauger n. gen. and Myurellopsis n. gen. each include about a dozen species. The first is restricted to the deep waters of the Indo-West Pacific, while the latter two range widely in both geographic and bathymetric distribution. Neoterebra n. gen. encompasses about 65 species from a range of localities in the eastern Pacific, Caribbean, and Atlantic, and from varying depths. To characterize the highly diversified genera Terebra, Punctoterebra, Myurella and Duplicaria, each of which comprise several morphological clusters, we propose the use of DNA-based diagnoses. These diagnoses are combined with more informative descriptions to define most of the supraspecific taxa of Terebridae, to provide a comprehensive revision of the group.
???msg.biblio.biblioSurvey.label??? (20) [+] [-]ATIMO VATAE, CONCALIS, EXBODI, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MADEEP, ???msg.security.private???, MIRIKY, MUSORSTOM 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006, TERRASSES, ???msg.security.private???, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A.E., Zaharias P., Lemarcis T., Modica M.V., Holford M., Oliverio M., Kantor Y.I. & Puillandre N. 2024. Phylogenomics of Neogastropoda: The Backbone Hidden in the Bush, in Whelan N. (Ed.), Systematic Biology: syae010. DOI:10.1093/sysbio/syae010
???msg.biblio.abstract.label??? [+] [-]Abstract The molluskan order Neogastropoda encompasses over 15,000 almost exclusively marine species playing important roles in benthic communities and in the economies of coastal countries. Neogastropoda underwent intensive cladogenesis in the early stages of diversification, generating a “bush” at the base of their evolutionary tree, which has been hard to resolve even with high throughput molecular data. In the present study to resolve the bush, we use a variety of phylogenetic inference methods and a comprehensive exon capture dataset of 1817 loci (79.6% data occupancy) comprising 112 taxa of 48 out of 60 Neogastropoda families. Our results show consistent topologies and high support in all analyses at (super)family level, supporting monophyly of Muricoidea, Mitroidea, Conoidea, and, with some reservations, Olivoidea and Buccinoidea. Volutoidea and Turbinelloidea as currently circumscribed are clearly paraphyletic. Despite our analyses consistently resolving most backbone nodes, 3 prove problematic: First, the uncertain placement of Cancellariidae, as the sister group to either a Ficoidea-Tonnoidea clade or to the rest of Neogastropoda, leaves monophyly of Neogastropoda unresolved. Second, relationships are contradictory at the base of the major “core Neogastropoda” grouping. Third, coalescence-based analyses reject monophyly of the Buccinoidea in relation to Vasidae. We analyzed phylogenetic signal of targeted loci in relation to potential biases, and we propose the most probable resolutions in the latter 2 recalcitrant nodes. The uncertain placement of Cancellariidae may be explained by orthology violations due to differential paralog loss shortly after the whole genome duplication, which should be resolved with a curated set of longer loci.
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, CORSICABENTHOS 1, DongSha 2014, EXBODI, ILES DU SALUT, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, NanHai 2014, PAPUA NIUGINI, TAIWAN 2013, Tuhaa Pae 2013, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fricke R. 2017. Epigonus okamotoi, a new species of deepwater cardinalfish from New Britain, Papua New Guinea, Solomon Sea, western Pacific Ocean (Teleostei: Epigonidae). FishTaxa 2(3): 116-122
???msg.biblio.abstract.label??? [+] [-]A new species of deepwater cardinalfish, Epigonus okamotoi from off southwestern New Britain, Papua New Guinea, is described on the basis of a single specimen collected with a trawl in 315-624 m depth in Ainto Bay. The new species is characterised by the following characters: dorsal-fin rays VII+I, 9; pectoral-fin rays 15; total gill rakers 22; pyloric caeca 4; pored lateral-line scales 47+4; scales below lateral line 8; vertebrae 10+15; opercular spine present; maxillary mustache-like process absent; ribs absent on last abdominal vertebra; upper margin of pectoral-fin base on level or upper margin of pupil; proximal radial of first anal-fin pterygiophore slender; mouth cavity light grey. The new species is compared with other species in the genus.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Fricke R. 2018. Two new species of stargazers of the genus Uranoscopus (Teleostei: Uranoscopidae) from the western Pacific Ocean. Zootaxa 4476(1): 157-167. DOI:10.11646/zootaxa.4476.1.15
???msg.biblio.abstract.label??? [+] [-]Two new species of stargazers in the Uranoscopus albesca species-complex of the family Uranoscopidae are described from Papua New Guinea, which shares among other characters a concave posterodorsal margin of the pectoral fin. Uranoscopus brunneus n. sp. is described from a single specimen from off southwestern New Britain, and is characterised by lower edge of preopercle with 8 spines; labial fimbriae poorly-developed; anterior nostril with a long tubiform valve, posterior nostril a slit-like pore; supracleithrum with a sharp spine at rear end and five small spines inside; dorsoposterior margin of pectoral fin concave; 62 oblique scale-rows along the sides of the body in adult; pectoral-fin membranes dark brown. Uranoscopus kishimotoi n. sp., described from a single specimen from West Sepik Province, is characterised by the lower edge of preopercle with 3 spines; no labial fimbriae; both anterior and posterior nostrils with long tubiform valves; supracleithrum with a sharp spine at rear end and one additional small spine inside; dorso-posterior margin of pectoral fin concave; 59 oblique scale-rows along the sides of the body in adult; upper pectoral-fin membranes pale, lower membranes brown. The distribution of the species in the U. albesca species-complex is discussed.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]???msg.security.private???, KAVIENG 2014, MADEEP, PAPUA NIUGINI, ???msg.security.private???, SANTO 2006
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Fricke R., Allen G.R., Amon D., Andréfouët S., Chen W.J., Kinch J., Mana R., Russell B.C., Tully D. & White W.T. 2019. Checklist of the marine and estuarine fishes of New Ireland Province, Papua New Guinea, western Pacific Ocean, with 810 new records. Zootaxa 4588(1): 1-360. DOI:10.11646/zootaxa.4588.1.1
???msg.biblio.abstract.label??? [+] [-]A checklist of the marine and estuarine fishes of New Ireland Province is presented, with special emphasis on Kavieng District, combining both previous and new records. After the recent KAVIENG 2014 expedition, a total of 1325 species in 153 families were recorded from the region. The largest families are the Gobiidae, Pomacentridae, Labridae, Serranidae, Apogonidae, Lutjanidae, Chaetodontidae, Blenniidae, Carangidae, Acanthuridae, Scaridae, Holocentridae, Syngnathidae, Lethrinidae and Scorpaenidae. A total of 810 fish species (61.1 % of the total marine and estuarine fish fauna) are recorded from New Ireland for the first time.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Fricke R. 2021. Plectranthias normanby, a new species of perchlet from Papua New Guinea, western Pacific (Teleostei: Serranidae). FishTaxa 20: 25-38
???msg.biblio.abstract.label??? [+] [-]The Normanby perchlet Plectranthias normanby n. sp. is described from off Normanby Island, Milne Bay Province, Papua New Guinea, Solomon Sea, western Pacific Ocean, based on 2 specimens collected at depths of 175-480 metres. The new species is characterised within the Plectranthias inermis species group by the dorsal in with 12 spines and 13 soft rays; no dorsal-fin rays filamentous; fourth dorsal-fin spine the longest, the spine length 2.25-2.34 in head; anal fin with 3 spines and 7 soft rays; pectoral-fin rays 13, none branched; branched caudal fin emarginate without filamentous rays; branched caudal-fin rays 13; no scales on anterior half of interorbital space; gill rakers 7 + 10-11; posterior margin of preopercle with 11-19 serrae, lower margin with 2 antrorse spines; lateral line incomplete, with 17 tubed scales; scales above lateral line to origin of dorsal fin 3½; scales below lateral line to origin of anal fin 9; circumpeduncular scales 14; cheek with ca. 5 diagonal rows of large scales; sides of body with a large, round black blotch, caudal peduncle with two dark brown spots. A key to the species of the Plectranthias-inermis species-group is presented.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Frolová P., Van Der Veer E., Fransen C.H.J.M. & ĎUriš Z. 2024. A review of Palaemonella (Decapoda: Caridea: Palaemonidae), with clarification of the taxonomic status of Cuapetes americanus, Eupontonia and Vir, in Ahyong S. (Ed.), Invertebrate Systematics 38(4). DOI:10.1071/IS23055
???msg.biblio.abstract.label??? [+] [-]The pantropical genus Palaemonella Dana, 1852 (Caridea: Palaemonidae) currently includes 27 species of free-living and symbiotic marine shrimps. The monophyly of Palaemonella with respect to several closely related genera, however, has been questioned by recent analyses. We tested the monophyly of Palaemonella based on multigene phylogenetic analysis and the genus was revealed to be a paraphyletic assemblage by inclusion of species of the genera Eupontonia Bruce, 1971 and Vir Holthuis, 1952, and two genetic lineages of the western Atlantic Cuapetes americanus (Kingsley, 1878). We recognise one of the latter lineages as the previously described Periclimenes rhizophorae Lebour, 1949. Eupontonia and Vir are synonymised with Palaemonella. We also transfer Cuapetes americanus and Periclimenes rhizophorae to Palaemonella. Species previously assigned to Vir were revised; V. colemani Bruce, 2003, V. orientalis (Dana, 1852), V. philippinensis Bruce & Svoboda, 1984 and V. smiti Fransen & Holthuis, 2007 are regarded as valid species of Palaemonella; Vir longidactylus Marin, 2008 is synonymised with P. smiti; and the status of V. euphyllius Marin & Anker, 2005 remains unresolved. Palaemonella is currently regarded as a taxon with variable states of two main diagnostic characters, i.e. the plesiomorphic mandibular palp (fully reduced in P. americana) and the hepatic tooth (fully reduced in former species of Vir and Eupontonia – evidently due to symbiotic modes of life). ZooBank: urn:lsid:zoobank.org:pub:7EEBC655-7EDE-4E46-BCB2-2A3BA16ED7DD
???msg.biblio.biblioSurvey.label??? (11) [+] [-]ATIMO VATAE, BORDAU 1, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, PAKAIHI I TE MOANA, PANGLAO 2004, PAPUA NIUGINI, PROTEUS-GUYANE, SANTO 2006
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Frolová P., Van Der Veer E., Fransen C.H.J.M. & ĎUriš Z. 2024. A review of Palaemonella (Decapoda: Caridea: Palaemonidae), with clarification of the taxonomic status of Cuapetes americanus, Eupontonia and Vir, in Ahyong S. (Ed.), Invertebrate Systematics 38(4). DOI:10.1071/IS23055
???msg.biblio.abstract.label??? [+] [-]The pantropical genus Palaemonella Dana, 1852 (Caridea: Palaemonidae) currently includes 27 species of free-living and symbiotic marine shrimps. The monophyly of Palaemonella with respect to several closely related genera, however, has been questioned by recent analyses. We tested the monophyly of Palaemonella based on multigene phylogenetic analysis and the genus was revealed to be a paraphyletic assemblage by inclusion of species of the genera Eupontonia Bruce, 1971 and Vir Holthuis, 1952, and two genetic lineages of the western Atlantic Cuapetes americanus (Kingsley, 1878). We recognise one of the latter lineages as the previously described Periclimenes rhizophorae Lebour, 1949. Eupontonia and Vir are synonymised with Palaemonella. We also transfer Cuapetes americanus and Periclimenes rhizophorae to Palaemonella. Species previously assigned to Vir were revised; V. colemani Bruce, 2003, V. orientalis (Dana, 1852), V. philippinensis Bruce & Svoboda, 1984 and V. smiti Fransen & Holthuis, 2007 are regarded as valid species of Palaemonella; Vir longidactylus Marin, 2008 is synonymised with P. smiti; and the status of V. euphyllius Marin & Anker, 2005 remains unresolved. Palaemonella is currently regarded as a taxon with variable states of two main diagnostic characters, i.e. the plesiomorphic mandibular palp (fully reduced in P. americana) and the hepatic tooth (fully reduced in former species of Vir and Eupontonia – evidently due to symbiotic modes of life).
???msg.biblio.biblioSurvey.label??? (12) [+] [-]ATIMO VATAE, BORDAU 1, GUYANE 2014, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, PAKAIHI I TE MOANA, PAPUA NIUGINI, PROTEUS-GUYANE, SANTO 2006
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Galil B.S. & Ng P. 2020. New and rare leucosiid crabs (Crustacea: Decapoda: Brachyura) from Papua New Guinea, Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:403-444, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]species are new records for Papua New Guinea: Alox ornatum (Ihle, 1918), A. tormos Galil & Ng, 2009; Arcania tuberculata Bell, 1855; Coralliocryptus caementa Komai & Ng, 2012; Cryptocnemus aberrans Balss, 1938; C. haddoni Calman, 1900; C. stimpsoni Ihle, 1915; Dolos petraeus (A. Milne-Edwards, 1874); Ebalia longispinosa Ihle, 1918; Ixa pulcherrima (Haswell, 1879); Kabutos durandi (Serène, 1955); Leucosia punctata Bell, 1855; Myra brevimana Alcock, 1896; Myrine kessleri (Paul’son, 1875); Nucia speciosa Dana, 1852; Nursia phylloides Ihle; 1918, Nursilia tonsor Alcock, 1896; Oreotlos lagarodes Tan & Ng, 1995; Pseudophilyra tenuipes Ihle, 1918 and Tokoyo cirrata Galil, 2003. Of these, two species, C. stimpsoni and N. phylloides, had only been known from single type specimens collected during the ‘Siboga’ Expedition (1899-1900). The new species of Cryptocnemus Stimpson, 1858, is described, illustrated and compared with congeners. Colour photographs are provided for 26 species.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Goulding T.C., Strong E.E. & Quattrini A.M. 2023. Target‐capture probes for phylogenomics of the Caenogastropoda. Molecular Ecology Resources 23(6): 1372-1388. DOI:10.1111/1755-0998.13793
???msg.biblio.abstract.label??? [+] [-]AbstractTarget‐capture approaches have facilitated a rapid growth in the field of phylogenomics but few probe sets exist for molluscs, an exceptionally rich phylum with unparalleled ecological and morphological diversity. We designed and tested the first universal probe set using Phyluce to capture ultraconserved elements (UCEs) and exon loci from the Subclass Caenogastropoda ‐ one of six major lineages of gastropods. The probe set consists of 29,441 probes designed to target 1142 UCE loci and 1933 exon loci (3075 total). In silico analyses of our probe set yielded an average of 2110 loci from genomes and 1389 loci from transcriptomes of diverse caenogastropods, from which an average of 1669 and 849 loci were retained respectively after screening to remove those that matched multiple contigs. Phylogenetic analyses of the loci extracted from transcriptomes produced well‐supported trees very similar to those published based on transcriptomic analyses. Phylogenetic relationships estimated from loci extracted from genomes recover similar phylogenetic relationships, and indicate that the loci targeted with this probe set are informative for resolving deep phylogenetic relationships. An in vitro analysis of the probe set with the Epitoniidae, a diverse caenogastropod family of uncertain affinity and with poorly resolved evolutionary relationships, recovered a total of 2850 loci. Although preliminary, the analysis of loci captured by our probe set for a small number of epitoniid taxa produced a well‐resolved tree indicating that this probe set is also able to resolve relationships at shallower hierarchical scales. Together, the in silico and in vitro analyses indicate that target‐capture enrichment with this probe set is a useful tool for reconstructing phylogenetic relationships across taxonomic levels and evolutionary time scales.
???msg.biblio.biblioSurvey.label??? (12) [+] [-]ATIMO VATAE, CORSICABENTHOS 2, KANACONO, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, SPANBIOS, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Hanafi-Portier M., Samadi S., Corbari L., Chan T.Y., Chen W.J., Chen J.N., Lee M.Y., Mah C., Saucède T., Borremans C. & Olu K. 2021. When Imagery and Physical Sampling Work Together: Toward an Integrative Methodology of Deep-Sea Image-Based Megafauna Identification. Frontiers in Marine Science 8: 749078. DOI:10.3389/fmars.2021.749078
???msg.biblio.abstract.label??? [+] [-]Imagery has become a key tool for assessing deep-sea megafaunal biodiversity, historically based on physical sampling using fishing gears. Image datasets provide quantitative and repeatable estimates, small-scale spatial patterns and habitat descriptions. However, taxon identification from images is challenging and often relies on morphotypes without considering a taxonomic framework. Taxon identification is particularly challenging in regions where the fauna is poorly known and/or highly diverse. Furthermore, the efficiency of imagery and physical sampling may vary among habitat types. Here, we compared biodiversity metrics (alpha and gamma diversity, composition) based on physical sampling (dredging and trawling) and towed-camera still images (1) along the upper continental slope of Papua New Guinea (sedimented slope with wood-falls, a canyon and cold seeps), and (2) on the outer slopes of the volcanic islands of Mayotte, dominated by hard bottoms. The comparison was done on selected taxa (Pisces, Crustacea, Echinoidea, and Asteroidea), which are good candidates for identification from images. Taxonomic identification ranks obtained for the images varied among these taxa (e.g., family/order for fishes, genus for echinoderms). At these ranks, imagery provided a higher taxonomic richness for hard-bottom and complex habitats, partially explained by the poor performance of trawling on these rough substrates. For the same reason, the gamma diversity of Pisces and Crustacea was also higher from images, but no difference was observed for echinoderms. On soft bottoms, physical sampling provided higher alpha and gamma diversity for fishes and crustaceans, but these differences tended to decrease for crustaceans identified to the species/morphospecies level from images. Physical sampling and imagery were selective against some taxa (e.g., according to size or behavior), therefore providing different facets of biodiversity. In addition, specimens collected at a larger scale facilitated megafauna identification from images. Based on this complementary approach, we propose a robust methodology for image-based faunal identification relying on a taxonomic framework, from collaborative work with taxonomists. An original outcome of this collaborative work is the creation of identification keys dedicated specifically to in situ images and which take into account the state of the taxonomic knowledge for the explored sites.
???msg.biblio.biblioSurvey.label??? (9) [+] [-]BENTHEDI, BIOMAGLO, BIOPAPUA, MADEEP, MAINBAZA, MIRIKY, ???msg.security.private???, ???msg.security.private???, PAPUA NIUGINI
???msg.biblio.codeCollection.label??? IC (Ichtyologie), IE (Échinodermes), IK (Cnidaires), IM (Mollusques), IP (Porifères), IU (Crustacés) -
Hibino Y., Chiu Y.C., Chen H.M. & Shao K.T. 2019. Two new species of the genus Ophichthus from the western central Pacific Ocean, with a redescription of Ophichthus megalops Asano, 1987 (Anguilliformes: Ophichthidae). Zootaxa 4702(1): 140-154. DOI:10.11646/zootaxa.4702.1.17
???msg.biblio.abstract.label??? [+] [-]Two new species similar to Ophichthus megalops Asano, 1987 with dark-tipped anal fins, are described on the basis of one specimen of each species. Ophichthus semilunatus sp. nov. from northeastern Taiwan is characterized by having 176 total vertebrae, three rows of teeth on the maxilla, one + three supraorbital pores, two preopercular pores, a brownish anterior-nostril tube, and a blotch on the anterior margin of anus. Ophichthus brevidorsalis sp. nov. from New Caledonia is characterized by having two preopercular pores, one + three supraorbital pores, smaller eyes 2.7 in head, a short head 9.5% of total length, a long tail 59.8% of total length, a slightly short snout 19.4% of head, and 43 predorsal vertebrae. A redescription of O. megalops is provided based on the holotype and 18 specimens newly collected from Taiwan. Selected characters of all nine Ophichthus with a dark-tipped anal fin are provided. In addition, partial COI sequences of five species is provided.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Houart R. 2017. Description of eight new species and one new genus of Muricidae (Gastropoda) from the Indo-West Pacific. Novapex 18(4): 81-113
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
HUANG S.I. & Lin M.H. 2021. Thirty Trichotropid CAPULIDAE in tropical and subtropical Indo-Pacific and Atlantic Ocean (GASTROPODA). Bulletin of Malacology, Taiwan 44: 23-81
???msg.biblio.abstract.label??? [+] [-]30 new species in the Trichotropid CAPULIDAE in the genera Verticosta, Latticosta n. gen., Torellia and Trichosirius are described from tropical and subtropical deep water of Indo-Pacific and Atlantic Ocean: Verticosta ariane n. sp., Verticosta bellefontainae n. sp., Verticosta milleinsularum n. sp., Verticosta filipinos n. sp., Verticosta plexa n. sp., Verticosta lapita n. sp., Verticosta pyramis n. sp., Verticosta kanak n. sp., Verticosta vanuatuensis n. sp., Verticosta feejee n. sp., Verticosta lilii n. sp., Verticosta sinusvellae n. sp., Verticosta terrasesae n. sp., Verticosta uvea n. sp., Verticosta rurutuana n. sp., Verticosta bicarinata n. sp., Verticosta tricarinata n. sp., Verticosta quadricarinata n. sp., Verticosta cheni n. sp., Verticosta iris n. sp., Verticosta castelli n. sp., Verticosta biangulata n. sp., Verticosta reunionnaise n. sp., Verticosta lemurella n. sp., Verticosta madagascarensis n. sp., Latticosta guidopoppei n. sp., Latticosta tagaroae n. sp., Latticosta magnifica n. sp., Torellia loyaute n. sp. and Trichosirius omnimarium n. sp. Trichotropis townsendi is now Latticosta townsendi n. comb.. Shell material comes from expeditions by MNHN and collections of authors.
???msg.biblio.biblioSurvey.label??? (51) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BENTHEDI, BIOCAL, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 1, BORDAU 2, CONCALIS, EBISCO, EXBODI, GUYANE 2014, HALIPRO 1, INHACA 2011, KANACONO, KARUBAR, KAVIENG 2014, LAGON, LIFOU 2000, MADEEP, MADIBENTHOS, MD32 (REUNION), MIRIKY, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 8, ???msg.security.private???, TAIWAN 2000, TARASOC, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Irwin A.R., Bouchet P., Crame J.A., Harper E.M., Kronenberg G.C., Strong E.E. & Williams S.T. 2024. Molecular phylogenetics of the superfamily Stromboidea (Caenogastropoda): New insights from increased taxon sampling. Zoologica Scripta: zsc.12685. DOI:10.1111/zsc.12685
???msg.biblio.abstract.label??? [+] [-]Abstract The superfamily Stromboidea is a clade of morphologically distinctive gastropods which include the iconic Strombidae, or ‘true conchs’. In this study, we present the most taxonomically extensive phylogeny of the superfamily to date, using fossil calibrations to produce a chronogram and extant geographical distributions to reconstruct ancestral ranges. From these results, we confirm the monophyly of all stromboidean families; however, six genera are not monophyletic using current generic assignments (Strombidae: Lentigo , Canarium , Dolomena , Doxander ; Xenophoridae: Onustus , Xenophora ). Within Strombidae, analyses resolve an Indo‐West Pacific (IWP) clade sister to an East Pacific/Atlantic clade, together sister to a second, larger IWP clade. Our results also indicate two pulses of strombid diversification within the Miocene, and a Tethyan/IWP origin for Strombidae—both supported by the fossil record. However, conflicts between divergence time estimates and the fossil record warrant further exploration. Species delimitation analyses using the COI barcoding gene support several taxonomic changes. We synonymise Euprotomus aurora with Euprotomus bulla , Strombus alatus with Strombus pugilis , Dolomena abbotti with Dolomena labiosa , and Dolomena operosa with Dolomena vittata . We identified cryptic species complexes within Terebellum terebellum , Lambis lambis , “Canarium” wilsonorum , Dolomena turturella and Maculastrombus mutabilis . We reinstate Rimellopsis laurenti as a species (previously synonymised with R. powisii ) and recognise Harpago chiragra rugosus and Lambis truncata sowerbyi valid at the rank of species. Finally, we establish several new combinations to render Lentigo , Dolomena , and Canarium monophyletic: Lentigo thersites , Dolomena robusta , Dolomena epidromis , Dolomena turturella , Dolomena taeniata , Dolomena vanikorensis , D. vittata , “Canarium” wilsonorum , Hawaiistrombus scalariformis , Maculastrombus mutabilis , Maculastrombus microurceus .
???msg.biblio.biblioSurvey.label??? (21) [+] [-]ATIMO VATAE, AURORA 2007, CONCALIS, CORSICABENTHOS 3, ???msg.security.private???, EXBODI, GUYANE 2014, ILES DU SALUT, INHACA 2011, KANACONO, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, KOUMAC 2.1, MADEEP, MADIBENTHOS, MIRIKY, PANGLAO 2004, PAPUA NIUGINI, SANTO 2006, Tuhaa Pae 2013
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y., Fedosov A. & Puillandre N. 2018. New and unusual deep-water Conoidea revised with shell, radula and DNA characters. Ruthenica, Russian Malacological Journal 28(2): 47-82. DOI:10.35885/ruthenica.2018.28(2).1
???msg.biblio.abstract.label??? [+] [-]In the course of preparation of a new molecular phylogeny of Conoidea based on exon-capture some new species and species with notable morphology were revealed. The taxonomy of these species is discussed and the radula of most of them illustrated for the first time. New genera are described: Comispira gen. nov. (Cochlespiridae), type species Leucosyrinx mai Li et Li, 2008; Pagodaturris gen. nov. (Clavatulidae), type species Pleurotoma molengraaffi Tesch, 1915. New species described: Comispira compta gen. et sp. nov., Sibogasyrinx sangeri sp. nov. (both Cochlespiridae), Pagodaturris philippinensis gen. et sp. nov. (Clavatulidae), Horaiclavus micans sp. nov., Iwaoa invenusta sp. nov. (both Horaiclavidae), Lucerapex cracens sp. nov., Lucerapex laevicarinatus sp. nov. (Turridae), Heteroturris kanacospira sp. nov. (Borsoniidae). Epideira Hedley, 1918 is reallocated from Pseudomelatomidae to Horaiclavidae. The radulae of Kuroshioturris nipponica (Shuto, 1961) (Turridae), Leucosyrinx verrillii (Dall, 1881), and Leucosyrinx luzonica (Powell, 1969) comb. nov. are illustrated for the first time.
???msg.biblio.biblioSurvey.label??? (19) [+] [-]AURORA 2007, BIOPAPUA, CEAMARC-AA, CONCALIS, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, MADEEP, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y., Bouchet P., Fedosov A., Puillandre N. & Zaharias P. 2024. Generic revision of the Recent Turridae (Neogastropoda: Conoidea). Journal of Molluscan Studies 90(5): eyae032. DOI:10.1093/mollus/eyae032
???msg.biblio.abstract.label??? [+] [-]ABSTRACT The family Turridae, once considered to encompass the entire diversity of Conoidea, excluding only the cone shells (family Conidae) and the auger shells (family Terebridae), has undergone significant redefinition based on both morphological and molecular data. Prior to this study, it included 15 Recent genera, comprising 209 species. However, a recent comprehensive analysis of an extensive dataset featuring 3,159 cytochrome c oxidase subunit I sequences has unveiled numerous species complexes, new species and previously undiscovered deep lineages. The newly proposed classification of Turridae based on an exon-capture phylogeny recognizes 24 clades, each worthy of genus rank, though only 13 of them had available names. As a result, 11 new genera have been described, namely Thielesyrinx n. gen., Shutogemmula n. gen., Mcleanigemmula n. gen., Pseudogemmula n. gen., Deceptigemmula n. gen., Oliveragemmula n. gen., Powelligemmula n. gen., Kilburnigemmula n. gen., Alisigemmula n. gen., Taylorigemmula n. gen. and Anisogemmula n. gen. With the exception of Thielesyrinx n. gen., species from all of these were previously classified within Gemmula, or Lophiotoma. Notably, some new genera, such as Deceptigemmula n. gen., Kilburnigemmula n. gen., Shutogemmula n. gen. and Taylorigemmula n. gen., cannot be morphologically differentiated, as similar species are found in other genera. Therefore, their distinction relies solely on molecular data. The name Eugemmula is re-instated from the synonymy of Gemmula. Purpuraturris is synonimized with Annulaturris, while Iotyrris with Xenuroturris. In total, we recognize 312 species/primary species hypotheses (PSHs) within the family. Molecular data were obtained for 212 species (among them 15 species complexes comprising in total 45 PSHs), mostly for the first time. A characteristic feature common to the entire family is the position of the relatively narrow anal sinus on the whorl periphery or immediately above it. Radula was examined in representatives of all genera. Although in several cases the radular morphology can aid genus differentiation (e.g. distinguishing Turris from Annulaturris), it is mostly a highly homoplastic structure, with very similar radular types occurring in distantly related genera.
???msg.biblio.biblioSurvey.label??? (33) [+] [-]ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, BOA1, CONCALIS, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2, KARUBENTHOS 2012, KOUMAC 2.1, MADEEP, MADIBENTHOS, MAINBAZA, MUSORSTOM 9, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, TAIWAN 2004, TAIWAN 2013, TARASOC, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y.I., Fedosov A.E., Snyder M.A. & Bouchet P. 2018. Pseudolatirus Bellardi, 1884 revisited, with the description of two new genera and five new species (Neogastropoda: Fasciolariidae). European Journal of Taxonomy 433: 1-57. DOI:10.5852/ejt.2018.433
???msg.biblio.abstract.label??? [+] [-]The genus Pseudolatirus Bellardi, 1884, with the Miocene type species Fusus bilineatus Hörnes, 1853, has been used for 13 Miocene to Early Pleistocene fossil species and eight Recent species and has traditionally been placed in the fasciolariid subfamily Peristerniinae Tryon, 1880. Although the fossil species are apparently peristerniines, the Recent species were in their majority suspected to be most closely related to Granulifusus Kuroda & Habe, 1954 in the subfamily Fusininae Wrigley, 1927. Their close affinity was confirmed by the molecular phylogenetic analysis of Couto et al. (2016). In the molecular phylogenetic section we present a more detailed analysis of the relationships of 10 Recent Pseudolatirus-like species, erect two new fusinine genera, Okutanius gen. nov. (type species Fusolatirus kuroseanus Okutani, 1975) and Vermeijius gen. nov. (type species Pseudolatirus pallidus Kuroda & Habe, 1961). Five species are described as new for science, three of them are based on sequenced specimens (Granulifusus annae sp. nov., G. norfolkensis sp. nov., Okutanius ellenae gen. et sp. nov.) and two (G. tatianae sp. nov., G. guidoi sp. nov.) are attributed to Granulifusus on the basis of conchological similarities to sequenced species. New data on radular morphology is presented for examined species.
???msg.biblio.biblioSurvey.label??? (60) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, BIOCAL, BIOGEOCAL, BORDAU 1, BORDAU 2, CHALCAL 2, CONCALIS, ???msg.security.private???, DongSha 2014, EBISCO, EXBODI, GEMINI, GUYANE 2014, HALICAL 1, HALIPRO 1, KANACONO, KARUBAR, KARUBENTHOS 2012, KAVIENG 2014, LAGON, LIFOU 2000, LITHIST, MADEEP, MD32 (REUNION), MIRIKY, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 1, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SANTO 2006, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, TAIWAN 2000, TARASOC, TERRASSES, VAUBAN 1978-1979, VOLSMAR, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y.I., Castelin M., Fedosov A. & Bouchet P. 2020. The Indo-Pacific Amalda (Neogastropoda, Olivoidea, Ancillariidae) revisited with molecular data, with special emphasis on New Caledonia. European Journal of Taxonomy 706: 1-52. DOI:10.5852/ejt.2020.706
???msg.biblio.abstract.label??? [+] [-]In the ancillariid genus Amalda, the shell is character rich and 96 described species are currently treated as valid. Based on shell morphology, several subspecies have been recognized within Amalda hilgendorfi, with a combined range extending at depths of 150–750 m from Japan to the South-West Pacific. A molecular analysis of 78 specimens from throughout this range shows both a weak geographical structuring and evidence of gene flow at the regional scale. We conclude that recognition of subspecies (richeri Kilburn & Bouchet, 1988, herlaari van Pel, 1989, and vezzaroi Cossignani, 2015) within A. hilgendorfi is not justified. By contrast, hilgendorfi-like specimens from the Mozambique Channel and New Caledonia are molecularly segregated, and so are here described as new, as Amalda miriky sp. nov. and A. cacao sp. nov., respectively. The New Caledonia Amalda montrouzieri complex is shown to include at least three molecularly separable species, including A. allaryi and A. alabaster sp. nov. Molecular data also confirm the validity of the New Caledonia endemics Amalda aureomarginata, A. fuscolingua, A. bellonarum, and A. coriolis. The existence of narrow range endemics suggests that the species limits of Amalda with broad distributions, extending, e.g., from Japan to Taiwan (A. hinomotoensis) or even Indonesia, the Strait of Malacca, Vietnam and the China Sea (A. mamillata) should be taken with caution.
???msg.biblio.biblioSurvey.label??? (41) [+] [-]ATIMO VATAE, BATHUS 1, BATHUS 2, BATHUS 3, BIOCAL, BIOPAPUA, CHALCAL 1, CONCALIS, EBISCO, EXBODI, HALIPRO 1, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2012, KAVIENG 2014, LAGON, MADEEP, MAINBAZA, MIRIKY, MUSORSTOM 4, MUSORSTOM 5, NORFOLK 1, NORFOLK 2, NanHai 2014, PANGLAO 2005, PAPUA NIUGINI, ???msg.security.private???, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 8, TERRASSES, VAUBAN 1978-1979, ???msg.security.private???, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y.I. & Puillandre N. 2021. Rare, deep-water and similar: revision of Sibogasyrinx (Conoidea: Cochlespiridae). European Journal of Taxonomy 773: 19-60. DOI:10.5852/ejt.2021.773.1509
???msg.biblio.abstract.label??? [+] [-]The genus Sibogasyrinx has to date included only four species of rare deep-water Conoidea, each known from few specimens. In shell characters it strongly resembles three distantly-related genera, two of which, Comitas and Leucosyrinx, belong to a different family, the Pseudomelatomidae. A molecular phylogenetic analysis of a large amount of material of Conoidea has revealed the existence of much additional undescribed diversity within Sibogasyrinx from the central Indo-Pacific and temperate Northern Pacific. Based on partial sequences of the mitochondrial cox1 gene and morphological characters of 54 specimens, 10 species hypotheses are proposed, of which six are described as new species: S. subula sp. nov., S. lolae sp. nov., S. maximei sp. nov., S. clausura sp. nov., S. pagodiformis sp. nov. and S. elbakyanae Kantor, Puillandre & Bouchet sp. nov. One of the previously described species was absent in our material. Most of the new species are very similar and are compared to Leucosyrinx spp. Species of Sibogasyrinx are unique among Conoidea on account of the high intrageneric variability in radular morphology. Three distinct radula types are found within Sibogasyrinx, two of which are confined to highly supported subclades.
???msg.biblio.biblioSurvey.label??? (16) [+] [-]AURORA 2007, BIOPAPUA, BOA1, EBISCO, EXBODI, GUYANE 2014, KANADEEP, KAVIENG 2014, MADEEP, MIRIKY, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kim J.N. & Chan T. 2020. Crangonid shrimps (Crustacea: Decapoda: Caridea) from Papua New Guinea, Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:207-238, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]Twenty-seven species of crangonid shrimps are reported from material collected in Papua New Guinea by the recent MNHN expeditions BIOPAPUA (2010), PAPUA NIUGINI (2012), MADEEP (2014), and KAVIENG (2014). All except Metacrangon punctata are first records for Papua New Guinea, including four new species, Metacrangon novaguinea n. sp., M. hayashii n. sp., Parapontophilus grandis n. sp., and Philocheras simulans n. sp.
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Komai T. & Sakiyama H. 2023. A new genus and new species of palaemonid shrimp (Decapoda: Caridea), associated with the deep-sea crinoid Metacrinus rotundus (Echinodermata: Isocrinidae), from Suruga Bay, Japan. Zootaxa 5380(3): 227-246. DOI:10.11646/zootaxa.5380.3.2
???msg.biblio.abstract.label??? [+] [-]Metacrimenes fenestra, a new palaemonid genus and species is described on the basis of an ovigerous female and one juvenile specimen from Suruga Bay, central Japan. The specimens were associated with the stalked crinoid Metacrinus rotundus Carpenter, 1885, collected at a depth of 131–200 m. Photographs taken in situ indicate that the shrimp lives ectosymbiotically on its crinoid host. The greatly reduced bud-like exopod on the third maxilliped links the new genus to Mesopontonia Bruce, 1967 (Indo-West Pacific) and Waldola Holthuis, 1951 (East Pacific), in which the exopod is absent, but the presence of antennal spine on the carapace and the non-elongate, symmetrical second pereopods immediately distinguish Metacrimenes n. gen. from these genera. Molecular phylogenetic analysis using a dataset concatenating two mitochondrial markers (16S rRNA and COI genes) clusters the new genus with Paraclimenes gorgonicola (Bruce, 1967), two species of Mesopontonia and Brucecaris tenuis (Bruce, 1969). However, in Paraclimenes Bruce, 1995 and Brucecaris Marin & Chan, 2006, the third maxilliped exopod is normally developed, flagellum-like. Other differentiating characters between the new taxon and the presumably allied taxa are discussed.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Lavesque N., Daffe G., Glasby C., Hourdez S. & Hutchings P. 2022. Three new deep-sea species of Marphysa (Annelida, Eunicida, Eunicidae) from Papua New Guinea (Bismarck and Solomon seas). ZooKeys 1122: 81-105. DOI:10.3897/zookeys.1122.89990
???msg.biblio.abstract.label??? [+] [-]Three new species of Marphysa Quatrefages, 1866, Marphysa bananasp. nov., Marphysa papuaensissp. nov., and Marphysa zanolaesp. nov. are described from deep-sea sunken vegetation off Papua New Guinea, using both morphology and molecular data (for two species). With the presence of compound spinigers only and the branchiae present over many chaetigers, Marphysa bananasp. nov. belongs to the group B2. This species is characterised by the presence of eyes, the presence of branchiae starting from chaetiger 20, and by the presence of three types of pectinate chaetae and bidentate subacicular hooks starting from chaetigers 13–52. With the presence of compound falcigers only and the branchiae restricted to a short anterior region, Marphysa papuaensissp. nov. belongs to the group C1. This species has a bilobed prostomium but no eyes, has branchiae from chaetigers 7 to 14–16 with up to 16 filaments. Marphysa papuaensissp. nov. is also characterised by the presence of bidentate subacicular hooks from chaetiger 20 and by a single type of pectinate chaetae. Finally, Marphysa zanolaesp. nov. belongs to the group C2, with the presence of compound falcigers only and the branchiae present over many chaetigers. This species is characterised by the absence of eyes, by the presence of branchiae with a single long filament starting from chaetiger 31, by unidentate subacicular hooks starting from chaetiger 28 and finally by one type of pectinate chaetae with very long outer teeth.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IA (Annélides, Polychètes et Sipunculides) -
Lavesque N., Nogueira J.M.M., Daffe G. & Hutchings P. 2024. Five new species of Terebellides (Annelida, Polychaeta, Trichobranchidae) from Papua New Guinea (Bismarck and Solomon seas). Frontiers in Ecology and Evolution 12: 1349362. DOI:10.3389/fevo.2024.1349362
???msg.biblio.abstract.label??? [+] [-]Five new species of Terebellides are described from coastal and deep waters of Papua New Guinea, using both morphology and molecular tools (for four species). Terebellides elenae n. sp. is characterized by the absence of both a glandular lateral region on TC3 and papillae on margins of the branchial lamellae and by the presence of partially fused branchial lobes with conspicuous fifth lobe and dorsal rounded projections until TC6. Terebellides fauchaldi n. sp. has a very large glandular lateral region on the third thoracic chaetiger (TC3), a fifth branchial lobe and partially fused branchial lobes, and conspicuous dorsal rounded projections on TC2–6. Terebellides madeep n. sp. is characterized by a thin glandular region on TC3 and by four free branchial lobes. Terebellides oculata n. sp. is one of the only two species in the world to have eyespots. Finally, T. papillosa n. sp. has geniculate chaetae on TC6 and TC7 and bears a large number of papillae. A majority-rule consensus tree using the 16S gene and an identification key for all Terebellides species described from the Central Indo-Pacific region are provided.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IA (Annélides, Polychètes et Sipunculides) -
Lee B.Y., De Forges B.R. & Ng P.K.L. 2019. Deep-sea spider crabs of the family Epialtidae MacLeay, 1838, from PapuaNew Guinea, with a redefinition of Tunepugettia Ng, Komai & Sato, 2017, and descriptions of two new genera (Crustacea: Decapoda: Brachyura: Majoidea). Zootaxa 4619(1): 1-44. DOI:10.11646/zootaxa.4619.1.1
???msg.biblio.abstract.label??? [+] [-]The deep-water epialtid spider crab (superfamily Majoidea) material collected from recent French expeditions to Papua New Guinea (BIOPAPUA 2010, PAPUA NIUGINI 2012, MADEEP 2014, and KAVIENG 2014) was studied. In addition to several new records for the country, five new species of Oxypleurodon Miers, 1885, Rochinia A. Milne-Edwards, 1875, and Tunepugettia Ng, Komai & Sato, 2017, are described. The taxonomy of Tunepugettia is reappraised, and a new genus, Crocydocinus n. gen., is established, characterised by its smooth ambulatory legs and a distinct male first gonopod structure. Four species from the Bay of Bengal, Sumatra, and Réunion Island, currently placed in Rochinia and Tunepugettia are transferred to Crocydocinus n. gen. and four new species from Papua New Guinea, Philippines, and Vanuatu are described. A new genus, Neophrys n. gen., with one new species from Papua New Guinea, is established, and is characterised by the supraorbital eave being fused with the carapace and the poorly developed pre-orbital angle.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Lee B.Y., Richer de Forges B. & Ng P.K.L. 2021. The generic affinities of the Indo-West Pacific species assigned to Rochinia A. Milne-Edwards, 1875 (Crustacea: Brachyura: Majoidea: Epialtidae). Raffles Bulletin of Zoology 69: 19-44. DOI:10.26107/RBZ-2021-0004
???msg.biblio.abstract.label??? [+] [-]The single most species-rich genus in the majoid family Epialtidae MacLeay, 1838, is Rochinia A. Milne-Edwards, 1875. Ng et al. (2008) listed 34 species and since then the number of species has continued to grow, especially in the Indo-West Pacific region (see Takeda, 2001; Takeda & Komatsu, 2005; Ng & Richer de Forges, 2007; Richer de Forges & Poore, 2008; Takeda, 2009; McLay, 2009; Ng & Richer de Forges, 2013; Richer de Forges & Ng, 2013; Takeda & Marumura, 2014; Lee et al., 2017; Lee et al., 2019). The systematic problems with the genus are well known; Rochinia, as defined by Griffin & Tranter (1986a) was too broad and clearly polyphyletic. Rochinia sensu Griffin & Tranter (1986a) includes four synonyms: Sphenocarcinus A. Milne-Edwards, 1875, Scyramathia A. Milne-Edwards, 1880, Anamathia Smith, 1885, and Oxypleurodon Miers, 1885. Griffin & Tranter (1986a) also transferred three species that were described under Hyastenus White, 1847, and Pugettia Dana, 1851, to Rochinia. Goniopugettia Sakai, 1986, a genus overlooked by Griffin & Tranter (1986a), included Rochinia sagamiensis (Gordon, 1930), and was recognised by Ng et al.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]AURORA 2007, BIOPAPUA, DongSha 2014, KAVIENG 2014, MADEEP, MUSORSTOM 5, NanHai 2014, PANGLAO 2005, SALOMONBOA 3, TARASOC, ZhongSha 2015
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Lee H., Puillandre N., Kano Y., Chen W.J. & Samadi S. 2022. Biodiversity and phylogeny of Cocculinidae (Gastropoda: Cocculinida) in the Indo-West Pacific. Zoological Journal of the Linnean Society 196(1): 366-392. DOI:10.1093/zoolinnean/zlac023
???msg.biblio.abstract.label??? [+] [-]Abstract The family Cocculinidae (Gastropoda: Cocculinida) consists of small, usually colourless benthic limpets living primarily at depths below 100 m, and on decaying plant or animal remains. These habitats are difficult to sample and the knowledge about Cocculinidae species diversity, biogeography, ecology and evolution is therefore poor. To explore the species diversity of the Cocculinidae, we examined 499 specimens collected from 196 sites, mainly explored during expeditions of the ‘Tropical Deep-Sea Benthos’ programme in the Indo-West Pacific (IWP). To propose a species hypotheses, we used an integrated approach to taxonomy in which we combined DNA-based methods, with morphological, geographical and ecological considerations. To classify the species hypotheses into genera, we used a combination of one mitochondrial and two nuclear gene fragments to reconstruct a phylogenetic tree. We then used six morphological characters to diagnose the identified genera. Our results revealed an exceptionally high diversity of IWP Cocculinidae, with 51 species hypotheses that were mostly not assigned to available species names. We also discovered a previously unknown type of copulatory structure in the group. At a higher taxonomic level, we identified ten main clades in the family. Although six of them matched existing genera, four others should be regarded as new genera awaiting formal description.
???msg.biblio.biblioSurvey.label??? (21) [+] [-]AURORA 2007, BIOPAPUA, BOA1, CONCALIS, DongSha 2014, EBISCO, EXBODI, KAVALAN 2018, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2013
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Lee S.H., Lee M.Y., Matsunuma M. & Chen W.J. 2019. Exploring the Phylogeny and Species Diversity of Chelidoperca (Teleostei: Serranidae) From the Western Pacific Ocean by an Integrated Approach in Systematics, With Descriptions of Three New Species and a Redescription of C. lecromi Fourmanoir, 1982. Frontiers in Marine Science 6: 465. DOI:10.3389/fmars.2019.00465
???msg.biblio.abstract.label??? [+] [-]With 11 species, the genus Chelidoperca is a small group of teleost fishes belonging to the Serranidae. They are bottom-dwelling fishes living on continental shelves/slopes in offshore areas or on remote seamounts/banks at depths ranging from around 40–400m mostly in the tropical Indo-West Pacific. Over the past few years, efforts have been made to resolve the taxonomy of Chelidoperca, and subsequently four new species were described. However, these recent advances were made with a traditional approach (i.e., morphology) and limited examinable materials, usually preserved specimens, from ichthyological collections. Further investigations are still needed to address the gaps in our knowledge about their diversity, phylogeny, and biogeography. In this study, we collected 65 new samples, mainly during eight biodiversity expeditions carried out between 2007 and 2016 in the West Pacific under the Tropical Deep-Sea Benthos program. Specimens were photographed after collection to record fresh color patterns, which are essential for species diagnosis. Our analytical approach includes state-of-the-art DNA-based methods for species delimitation. The combined evidence from both molecular and morphological examinations, as well as other information such as geography, is used to test species validity. This reveals 15 species, including six new ones. We formally describe herein C. leucostigmata sp. nov., C. microdon sp. nov., and C. barazeri sp. nov. on the basis of specimens collected on Macclesfield Bank in the South China Sea, on the Chesterfield and Island of Pines plateau of New Caledonia, and off the New Ireland Province of Papua New Guinea, respectively. These new species are morphologically distinct from all other known species of Chelidoperca by body color pattern and combinations of a few identified characters. We also redescribe one of the lesser known species, C. lecromi, from fresh specimens collected close to its type locality and a new site in the Coral Sea. The distributional records for this and other known species are updated accordingly. Genetic references of the species as well as an updated identification key to western Pacific species are also provided.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Lemaitre R., Rahayu D.L. & Komai T. 2018. A revision of “blanket-hermit crabs” of the genus Paguropsis Henderson, 1888, with the description of a new genus and five new species (Crustacea, Anomura, Diogenidae). ZooKeys 752: 17-97. DOI:10.3897/zookeys.752.23712
???msg.biblio.abstract.label??? [+] [-]For 130 years the diogenid genus Paguropsis Henderson, 1888 was considered monotypic for an unusual species, P. typica Henderson, 1888, described from the Philippines and seldom reported since. Although scantly studied, this species is known to live in striking symbiosis with a colonial sea anemone that the hermit can stretch back and forth like a blanket over its cephalic shield and part of cephalothoracic appendages, and thus the common name “blanket-crab”. During a study of paguroid collections obtained during recent French-sponsored biodiversity campaigns in the Indo-West Pacific, numerous specimens assignable to Paguropsis were encountered. Analysis and comparison with types and other historical specimens deposited in various museums revealed the existence of five undescribed species. Discovery of these new species, together with the observation of anatomical characters previously undocumented or poorly described, including coloration, required a revision of the genus Paguropsis. The name Chlaenopagurus andersoni Alcock & McArdle, 1901, considered by Alcock (1905) a junior synonym of P. typica, proved to be a valid species and is resurrected as P. andersoni (Alcock, 1899). In two of the new species, the shape of the gills, length/width of exopod of maxilliped 3, width and shape of sternite XI (of pereopods 3), and armature of the dactyls and fixed fingers of the chelate pereopods 4, were found to be characters so markedly different from P. typica and other species discovered that a new genus for them, Paguropsina gen. n., is justified. As result, the genus Paguropsis is found to contain five species: P. typica, P. andersoni, P. confusa sp. n., P. gigas sp. n., and P. lacinia sp. n. Herein, Paguropsina gen. n., is proposed and diagnosed for two new species, P. pistillata gen. et sp. n., and P. inermis gen. et sp. n.; Paguropsis is redefined, P. typica and its previously believed junior synonym, P. andersoni, are redescribed. All species are illustrated, and color photographs provided. Also included are a summary of the biogeography of the two genera and all species; remarks on the significance of the unusual morphology; and remarks on knowledge of the symbiotic anemones used by the species. To complement the morphological descriptions and assist in future population and phylogenetic investigations, molecular data for mitochondrial COI barcode region and partial sequences of 12S and 16S rRNA are reported. A preliminary phylogenetic analysis using molecular data distinctly shows support for the separation of the species into two clades, one with all five species of Paguropsis, and another with the two species Paguropsina gen. n.
???msg.biblio.biblioSurvey.label??? (28) [+] [-]BATHUS 3, BIOPAPUA, BORDAU 1, BORDAU 2, CORINDON 2, ???msg.security.private???, ???msg.security.private???, EBISCO, KARUBAR, LIFOU 2000, LITHIST, LUMIWAN 2008, MADEEP, MAINBAZA, MIRIKY, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 5, MUSORSTOM 6, NORFOLK 1, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, SALOMON 1, SALOMON 2, ZhongSha 2015
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Lunina A.A., Kulagin D.N. & Vereshchaka A.L. 2018. Oplophoridae (Decapoda: Crustacea): phylogeny, taxonomy and evolution studied by a combination of morphological and molecular methods. Zoological Journal of the Linnean Society. DOI:10.1093/zoolinnean/zly039
???msg.biblio.abstract.label??? [+] [-]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.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]???msg.security.private???, BIOPAPUA, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, MUSORSTOM 3, SALOMONBOA 3
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Macpherson E., Rodríguez-Flores P.C. & Machordom A. 2020. New occurrences of squat lobsters of the genus Eumunida Smith, 1883 (Decapoda, Eumunididae) in New Caledonia, the Solomon Islands and Papua-New Guinea, with the description of a new species. Zootaxa 4786(4): 485-496. DOI:10.11646/zootaxa.4786.4.2
???msg.biblio.abstract.label??? [+] [-]Examination of numerous specimens of squat lobsters of the genus Eumunida Smith, 1883 collected by French cruises along the coasts of New Caledonia, the Solomon Islands and Papua-New Guinea revealed the presence of six species, including a new species. The collection data of all of these species are recorded. The new species, E. turbulenta n. sp., is described and illustrated from New Caledonia and Chesterfield Islands.
???msg.biblio.biblioSurvey.label??? (18) [+] [-]BATHUS 2, BATHUS 3, BERYX 11, BIOPAPUA, CHALCAL 2, EBISCO, EXBODI, HALIPRO 1, HALIPRO 2, KANACONO, KANADEEP, MADEEP, NORFOLK 1, PAPUA NIUGINI, SALOMON 1, SMIB 10, SMIB 8, TERRASSES
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Macpherson E., Rodriguez-Flores P. & Machordom A. 2020. Squat lobsters of the families Munididae and Munidopsidae from Papua New Guinea, Deep-Sea Crustaceans from Papua New Guinea 31. Tropical deep-sea benthos Mémoires du Muséum national d’Histoire naturelle 213, Paris:11-120, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]More than 5000 specimens of squat lobsters belonging to the families Munididae and Munidopsidae were collected during four cruises along the coasts of Papua New Guinea. The study of these specimens revealed the presence of 13 new species (one Babamunida, one Crosnierita, eight Munida, one Paramunida and two Munidopsis). Overall, 109 species of Munididae and 37 of Munidopsidae are recognized. We include the records of all species, describing and illustrating the new species. Furthermore, we provide some new data on the colour patterns for some species. We have also included molecular data from two mitochondrial markers (16S rRNA and COI) to support the taxonomic status of different new species.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Macpherson E., Rodríguez-Flores P.C. & Machordom A. 2023. Integrative approach to describe new species of squat lobsters of the genera Heteronida Baba & de Saint Laurent, 1996 and Torbenella Baba, 2008 (Decapoda, Munididae) from the Southwestern Pacific Ocean. European Journal of Taxonomy 860. DOI:10.5852/ejt.2023.860.2055
???msg.biblio.abstract.label??? [+] [-]Specimens of munidid squat lobsters belonging to the genera Heteronida Baba & de Saint Laurent, 1996 and Torbenella Baba, 2008 were collected in scientific expeditions made by several French cruises along the southwestern Pacific. These specimens were identified as two species (one new) of Heteronida and six species (four new) of Torbenella. The present paper provides systematic accounts of the five new species, along with new locality records of known species shown by this material and color information where available. Molecular data is provided to support the systematic status of each new species. A key to species for each of the genera is also presented.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]BIOPAPUA, BORDAU 2, EBISCO, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, MUSORSTOM 7, PAPUA NIUGINI, SPANBIOS
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Macpherson E., Rodríguez-Flores P.C. & Machordom A. 2024. DNA barcoding and morphology revealed the existence of seven new species of squat lobsters in the family Munididae (Decapoda, Galatheoidea) in the southwestern Pacific. ZooKeys 1188: 91-123. DOI:10.3897/zookeys.1188.114984
???msg.biblio.abstract.label??? [+] [-]Specimens of squat lobsters belonging to the family MunididaeAhyong et al., 2010, representing the genera Garymunida Macpherson & Baba, 2022, Trapezionida Macpherson & Baba, 2022 and Typhlonida Macpherson & Baba, 2022, were collected during several cruises around New Caledonia and Papua New Guinea, Southwest Pacific. The integrative study of these specimens revealed the presence of one new species in Garymunida , five in Trapezionida and one in Typhlonida . We describe and illustrate these new species, providing some new data on the taxonomy of several rare or scarcely studied species of Trapezionida . Molecular data from different markers (mitochondrial and nuclear) was also included, based on data availability, to support the taxonomic status of different species. Finally, a key to species for each genus is also provided.
???msg.biblio.biblioSurvey.label??? (12) [+] [-]BIOPAPUA, EBISCO, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, NORFOLK 2, PAPUA NIUGINI, SPANBIOS, TARASOC, TERRASSES
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Mana R.R. 2020. FOREWORD / PRÉFACE, Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:9-10, ISBN:978-2-85653-913-2
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Modica M.V., Gorson J., Fedosov A.E., Malcolm G., Terryn Y., Puillandre N. & Holford M. 2020. Macroevolutionary Analyses Suggest That Environmental Factors, Not Venom Apparatus, Play Key Role in Terebridae Marine Snail Diversification, in Serb J. (Ed.), Systematic Biology 69(3): 413-430. DOI:10.1093/sysbio/syz059
???msg.biblio.abstract.label??? [+] [-]Abstract How species diversification occurs remains an unanswered question in predatory marine invertebrates, such as sea snails of the family Terebridae. However, the anatomical disparity found throughput the Terebridae provides a unique perspective for investigating diversification patterns in venomous predators. In this study, a new dated molecular phylogeny of the Terebridae is used as a framework for investigating diversification of the family through time, and for testing the putative role of intrinsic and extrinsic traits, such as shell size, larval ecology, bathymetric distribution, and anatomical features of the venom apparatus, as drivers of terebrid species diversification. Macroevolutionary analysis revealed that when diversification rates do not vary across Terebridae clades, the whole family has been increasing its global diversification rate since 25 Ma. We recovered evidence for a concurrent increase in diversification of depth ranges, while shell size appeared to have undergone a fast divergence early in terebrid evolutionary history. Our data also confirm that planktotrophy is the ancestral larval ecology in terebrids, and evolutionary modeling highlighted that shell size is linked to larval ecology of the Terebridae, with species with long-living pelagic larvae tending to be larger and have a broader size range than lecithotrophic species. Although we recovered patterns of size and depth trait diversification through time and across clades, the presence or absence of a venom gland (VG) did not appear to have impacted Terebridae diversification. Terebrids have lost their venom apparatus several times and we confirm that the loss of a VG happened in phylogenetically clustered terminal taxa and that reversal is extremely unlikely. Our findings suggest that environmental factors, and not venom, have had more influence on terebrid evolution.
???msg.biblio.biblioSurvey.label??? (14) [+] [-]ATIMO VATAE, EXBODI, INHACA 2011, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, NanHai 2014, PANGLAO 2005, SALOMON 2, SANTO 2006, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Nappo A. & Cilia D.P. 2025. Taxonomic review of the genus Korrigania Sanders et al., 2020 including a new species description, with comments on Tritonoranella Oyama, 1964 (Gastropoda: Bursidae). Bollettino Malacologico 61(1): 18-55. DOI:10.53559/BollMalacol.2024.17
???msg.biblio.abstract.label??? [+] [-]The taxonomic status of Korrigania Sanders et al., 2020, of the family Bursidae Thiele, 1925, is reviewed. Prior to the present work, the genus included five recent species that demonstrate considerable morphological variation. Herein, the new species Korrigania stefanoelisa n. sp., from New Caledonia and Vanuatu, is added, and K. vianelloi Cossignani, 2023, so far only known from the Philippines, is designated as synonym of K. awatii (Ray, 1950) n. syn. The main morphological characters of Korrigania are described, together with those of the species included. Bursa humilis Beu, 1981 and Bursa natalensis Coelho & Matthews, 1970 are accepted as Tritonoranella humilis (Beu, 1981) n. comb. and Tritonoranella natalensis (Coelho & Matthews, 1970) n. comb.
???msg.biblio.biblioSurvey.label??? (26) [+] [-]BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BIOCAL, BIOMAGLO, CONCALIS, EBISCO, EXBODI, HALICAL 1, KANACONO, KANADEEP, MADEEP, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, SAYA, TERRASSES, VAUBAN 1978-1979, VOLSMAR
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Ng P.K.L. & Richer de Forges B. 2020. A revision of the deep-sea porter crabs of the genus Gordonopsis Guinot & Richer de Forges, 1995 (Crustacea, Decapoda, Brachyura, Homolidae), with descriptions of five new species. Raffles Bulletin of Zoology 68: 267307. DOI:10.26107/RBZ-2020-0023
???msg.biblio.abstract.label??? [+] [-]For the century to 2018, only one species of the deep-water porter crab Gordonopsis Guinot & Richer de Forges, 1995 (Brachyura, Homolidae), the type species, G. profundorum (Alcock & Anderson, 1899), was known, and only from a handful of specimens from the Indian Ocean. In 2019, two species were described from the eastern Indian and western Pacific Oceans. The present revision of available material, most of which was only collected in the last decade, adds five new species to the genus. This explosion in species numbers demonstrates just how poor our understanding is of deep-sea habitats and their constituent fauna.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K.L., Forges B.R.D. & Lee B.Y. 2023. New and rare deep-sea majoid crabs (Crustacea: Brachyura) from Papua New Guinea. Zootaxa 5318(1): 1-44. DOI:10.11646/zootaxa.5318.1.1
???msg.biblio.abstract.label??? [+] [-]Additional spider crab (superfamily Majoidea) material from four major French-led expeditions to the Papua New Guinea region were examined in this study. One new genus and four new species from the families Inachidae and Oregoniidae are described. Dorhynchus profundus n. sp. is close to D. rostratus (Sakai, 1932) but can easily be separated by the shape of the ambulatory dactylus and the proportionately lower protogastric spines. Achaeus pholcus n. sp. is unusual in that it occurs in deeper waters (beyond 500 m), and can be separated from A. lacertosus Stimpson, 1857, A. villosus Rathbun, 1916, and A. brevidactylus Sakai, 1938, by its distinctive carapace shape, structure of the frontal margin, regions of the carapace, antennular fossa, ambulatory dactylus, male pleon, and proportions of the chela. Parapleisticantha aie n. sp. is closest to P. japonica Yokoya, 1933, but differs in its proportionately longer carapace, more elongated basal antennal article, longer third maxilliped ischium and the relatively less curved male first gonopod with the distal part differently structured. A new genus (Orbicantha n. gen.) with one new species (Orbicantha sacrebleu n. gen., n. sp.) is also described; it is allied to Pleistacantha Miers, 1879, Parapleisticantha Yokoya 1933, and Pleisticanthoides Yokoya, 1933, but is distinctive in its subcircular carapace, shorter regions, short pseudorostral spines, possession of spines on the gastric, cardiac and branchial regions, some of which have rounded tips, a short ocular peduncle, a very short third antennal article, a quadrate epistome, and the more reduced P4 and P5. New records from the family Epialtidae are also reported: Griffinia gilloloensis (Rathbun, 1916), Hyastenus borradailei (Rathbun, 1907), and Oxypleurodon luzonicum (Rathbun, 1916). The taxonomy of Grypachaeus tenuicollis Takeda, 1978 (Oregoniidae) and Griffinia lappacea (Rathbun, 1918) (Epialtidae) is also discussed.
???msg.biblio.biblioSurvey.label??? (7) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K. & Richer de Forges B. 2017. On a collection of Homolidae from the South China Sea, with descriptions of two new species of Homologenus A. Milne-Edwards, in Henderson, 1888, and the identities of Homologenus malayensis Ihle, 1912, and Lamoha superciliosa (Wood-Mason, in Wood-Mason & Alcock, 1891). Raffles Bulletin of Zoology 65: 243-268
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Nocella E., Zvonareva S.S., Fassio G., Pica D., Buge B., Villa R., Puillandre N., Modica M.V. & Oliverio M. 2024. Spicy food for the egg-cowries: the evolution of corallivory in the Ovulidae (Gastropoda: Cypraeoidea). Frontiers in Marine Science 10: 1323156. DOI:10.3389/fmars.2023.1323156
???msg.biblio.abstract.label??? [+] [-]Introduction Host-parasite associations provide very useful models to study adaptive processes. We investigated the interaction between carnivorous marine gastropods, the Ovulidae or egg-cowries, and their cnidarian food targets. Ovulidae (Fleming, 1828), is a family of specialized carnivorous caenogastropods that feed by browsing on octocorals (Anthozoa: Octocorallia: Malacalcyonacea and Scleralcyonacea) or, to a much lesser degree, on antipatharians (Anthozoa: Hexacorallia: Antipatharia) and Stylasteridae (Hydrozoa: Hydroidolina: Anthoathecata). Very scanty information is available on the phylogenetic relationships and the degree of specificity of the relationship with the cnidarians of this corallivorous lineage, especially for deep-water taxa. Methods To assess taxonomic identifications and investigate cnidarian/ovulid relationships in the context of their evolution, we generated an extensive molecular dataset comprising two mitochondrial ( cox1 and 16S rDNA ) and one nuclear gene ( 28S rDNA ) from 524 specimens collected worldwide. The coral hosts of the ovulid species have been identified by integrating literature data with new records, employing morphological and/or molecular (the mitochondrial 16S rDNA and mtMSH , and the nuclear ITS2) markers. Results We obtained a molecular phylogenetic framework for the Ovulidae, time-calibrated with nine reliable fossil records. An ancestral state reconstruction allowed to identify Hexacorallia or Hydroidolina as the most likely ancestral cnidarian host for the Ovulidae. Discussion Our phylogenetic hypothesis revealed the existence of groups that do not completely correspond to the currently employed subfamilial arrangement. Concerning trophic ecology, while only pediculariines ( Pedicularia and allied) are associated with hydrozoans (Stylasteridae), our results suggest that some ovulid lineages shifted independently between octocorals and hexacorals.
???msg.biblio.biblioSurvey.label??? (26) [+] [-]ATIMO VATAE, AURORA 2007, BIOMAGLO, CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, SPANBIOS, ZhongSha 2015
???msg.biblio.codeCollection.label??? IK (Cnidaires), IM (Mollusques) -
Okamoto M., Chen W.J. & Shinohara G. 2018. Epigonus okamotoi (Perciformes: Epigonidae), a junior synonym of E. draco, with new distributional records for E. atherinoides and E. lifouensis in the West Pacific. Zootaxa 4476(1): 141-150. DOI:10.11646/zootaxa.4476.1.13
???msg.biblio.abstract.label??? [+] [-]Epigonus okamotoi Fricke, 2017 was originally described on the basis of a single specimen collected from New Britain, Papua New Guinea during one of the exploratory cruises (campaign: MADEEP) in 2014 organized under the Tropical Deep-Sea Benthos program. However, there are no clear differences in the meristic and morphometric characters between the holotype of the new species and specimens of E. draco Okamoto, 2015, including two additional specimens of the species found in the ichthyological collections in the NTUM. The genetic distance (p-distance) between the two “species” at the COI locus was negligible. Accordingly, the holotype of E. okamotoi is considered to be a specimen of E. draco, and the former nominal species is reduced to a junior synonym of E. draco. In addition, we rediagnose and report new distributional records for E. atherinoides (Gilbert, 1905) and E. lifouensis Okamoto & Motomura, 2013 in the West Pacific.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Okamoto M., Chen W.J. & Motomura H. 2020. New distributional records of three deepwater cardinalfishes Epigonus angustifrons, E. denticulatus, and E. exodon (Perciformes: Epigonidae) in the South Indian Ocean. Cybium 44(2): 165-168. DOI:10.26028/CYBIUM/2020-442-008
???msg.biblio.abstract.label??? [+] [-]Two specimens (189.7-210.3 mm in standard length: SL) of Epigonus angustifrons Abramov & Manilo, 1987 and two specimens (120.2-138.6 mm SL) of E. denticulatus Dieuzeide, 1950 (Epigonidae) were collected from the St. Paul Seamount, central South Indian Ocean. Also, a single specimen (131.0 mm SL) of E. exodon Okamoto & Motomura, 2012 was collected off Mayotte, Comoros Archipelago, western South Indian Ocean. These specimens represent the first records of the three species from the two mentioned areas. The present specimen of E. exodon is the third specimen collected since the original description and new morphological data for the species based on this additional specimen are provided.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Pante E., France S.C., Gey D., Cruaud C. & Samadi S. 2015. An inter-ocean comparison of coral endemism on seamounts: the case of Chrysogorgia. Journal of Biogeography 42(10): 1907-1918. DOI:10.1111/jbi.12564
???msg.biblio.biblioSurvey.label??? (10) [+] [-]BIOPAPUA, EXBODI, MADEEP, NORFOLK 2, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SMIB 4, TAIWAN 2013, TERRASSES
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Phuong M.A., Alfaro M.E., Mahardika G.N., Marwoto R.M., Prabowo R.E., Von Rintelen T., Vogt P.W.H., Hendricks J.R. & Puillandre N. 2019. Lack of Signal for the Impact of Conotoxin Gene Diversity on Speciation Rates in Cone Snails, in Serb J. (Ed.), Systematic Biology 68(5): 781-796. DOI:10.1093/sysbio/syz016
???msg.biblio.abstract.label??? [+] [-]Understanding why some groups of organisms are more diverse than others is a central goal in macroevolution. Evolvability, or the intrinsic capacity of lineages for evolutionary change, is thought to influence disparities in species diversity across taxa. Over macroevolutionary time scales, clades that exhibit high evolvability are expected to have higher speciation rates. Cone snails (family: Conidae, $>$900 spp.) provide a unique opportunity to test this prediction because their toxin genes can be used to characterize differences in evolvability between clades. Cone snails are carnivorous, use prey-specific venom (conotoxins) to capture prey, and the genes that encode venom are known and diversify through gene duplication. Theory predicts that higher gene diversity confers a greater potential to generate novel phenotypes for specialization and adaptation. Therefore, if conotoxin gene diversity gives rise to varying levels of evolvability, conotoxin gene diversity should be coupled with macroevolutionary speciation rates. We applied exon capture techniques to recover phylogenetic markers and conotoxin loci across 314 species, the largest venom discovery effort in a single study. We paired a reconstructed timetree using 12 fossil calibrations with species-specific estimates of conotoxin gene diversity and used trait-dependent diversification methods to test the impact of evolvability on diversification patterns. Surprisingly, we did not detect any signal for the relationship between conotoxin gene diversity and speciation rates, suggesting that venom evolution may not be the rate-limiting factor controlling diversification dynamics in Conidae. Comparative analyses showed some signal for the impact of diet and larval dispersal strategy on diversification patterns, though detection of a signal depended on the dataset and the method. If our results remain true with increased taxonomic sampling in future studies, they suggest that the rapid evolution of conid venom may cause other factors to become more critical to diversification, such as ecological opportunity or traits that promote isolation among lineages.
???msg.biblio.biblioSurvey.label??? (21) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, TAIWAN 2013, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Poore G.C.B. 2023. New records, one new genus and 21 new species of Callianassidae (Crustacea, Axiidea) from the Indo-West Pacific. Memoirs of Museum Victoria: 167-255. DOI:10.24199/j.mmv.2023.82.09
???msg.biblio.abstract.label??? [+] [-]Poore, G.C.B. 2023. New records, one new genus and 21 new species of Callianassidae (Crustacea, Axiidea) from the Indo-West Pacific. Memoirs of Museum Victoria 82: 167–255. The collections of ghost shrimps from the Indo-West Pacific that contributed to recent molecular phylogeny and resulting reclassification of Callianassidae (Poore et al., 2019; Robles et al., 2020) provide opportunities to review 11 genera and describe one new genus, redescribe existing species and describe 21 new species. Aqaballianassa aqabaensis (Dworschak, 2003), A. brevirostris (Sakai, 2002), A. lewtonae (Ngoc-Ho, 1994) are rediagnosed and Aqaballianassa papua sp. nov. from Papua New Guinea and Aqaballianassa seychellensis sp. nov. from the Seychelles are described as new. Three new species of Caviallianassa Poore, Dworschak, Robles, Mantelatto and Felder, 2019 are compared in a key with Caviallianassa cavifrons (Komai and Fujiwara, 2012): Caviallianassa arafura sp. nov. from the Arafura Sea, Caviallianassa riwo sp. nov. from Papua New Guinea and Caviallianassa moorea sp. nov. from French Polynesia. Callianassa thailandica Sakai, 2005 is treated as species inquirenda. No species of Cheramus Bate, 1888 occurs in the Indo-West Pacific despite the genus name having been widely used. Five species of Coriollianassa Poore, Dworschak, Robles, Mantelatto and Felder, 2019 are recognised and figured: C. sibogae (De Man, 1905), C. coriolisae (Ngoc-Ho, 2014) and new species, Coriollianassa mainbazae sp. nov. and Coriollianassa maputo sp. nov. from the Mozambique Channel, and Coriollianassa nyinggulu sp. nov. from the North West Australian slope. Darryllianassa felderi gen. et sp. nov. is described from Papua New Guinea. Necallianassa nosybeensis sp. nov. is described as a new species from Madagascar. Praedatrypaea Poore, Dworschak, Robles, Mantelatto and Felder, 2019 is rediagnosed. Thirteen species are recognised and most diagnosed; four species are described as new: Praedatrypaea jangamo sp. nov. and Praedatrypaea mozambiquensis sp. nov. from Mozambique, and Praedatrypaea mandu sp. nov. and Praedatrypaea ningaloo sp. nov. from the North West Shelf of Australia. Callianassa malaccaensis Sakai, 2002 is treated as a junior synonym of P. orientalis (Bate, 1888). A key to separate ten species of Praedatrypaea is presented. Pugnatrypaea Poore, Dworschak, Robles, Mantelatto and Felder, 2019 is rediagnosed and confined to three species. Rayllianassa Komai and Tachikawa, 2008 is rediagnosed and its species discussed. Rayllianassa amboinensis (De Man, 1888), a variable species, is rediagnosed; Callianassa ngochoae Sakai, 1999 and Callianassa sahul Poore, 2008 are treated as synonyms. Rayllianassa aurora sp. nov., Rayllianassa bifida sp. nov. and Rayllianassa huonensis sp. nov. are described as new species; the first two are associated with submerged wood at depths greater than 100 m. Rudisullianassa Poore, Dworschak, Robles, Mantelatto and Felder, 2019 is rediagnosed. Rudisullianassa rudisulcus Komai, Fujita and Maenosono, 2014 is discussed and partially illustrated; Rudisullianassa pandan sp. nov. is described as a new species from submerged wood. Spinicallianassa Poore, Dworschak, Robles, Mantelatto and Felder, 2019 is reviewed and a key is provided to five species; three species are described as new: Spinicallianassa bilbili sp. nov. from Papua New Guinea; Spinicallianassa papetoai sp. nov. from French Polynesia; and Spinicallianassa westralia sp. nov. from Western Australia. Callianassa parvula Sakai, 1988 is treated as a possible synonym of S. spinicauda (Komai, Maenosono and Fujita, 2014). Trypaea Dana, 1852 contains only T. australiensis Dana, 1852 and does not occur in the Indo-West Pacific as sometimes reported.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]AURORA 2007, BIOPAPUA, KAVIENG 2014, MADEEP, MAINBAZA, MUSORSTOM 3, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Poore G.C. 2020. Axiid and micheleid lobsters from Indo-West Pacific deep-sea environments (Crustacea: Decapoda: Axiidea: Axiidae, Micheleidae), Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:259-368, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]Eight species of deep-water porter crabs of the family Homolidae are recorded from Papua New Guinea from three MNHN-led cruises to these waters: Homola orientalis Henderson, 1888, Homola coriolisi Guinot & Richer de Forges, 1995, Homolomannia sibogae Ihle, 1912, Homolomannia occlusa Guinot & Richer de Forges, 1981, Paromolopsis boasi Wood-Mason in Wood-Mason & Alcock, 1891, Lamoha woodmasoni n. sp., Ihlopsis multispinosa (Ihle, 1912) and Latreillopsis gracilipes Guinot & Richer de Forges, 1981. Most are new records for the country, Lamoha woodmasoni n. sp. appears to be the Pacific sister species of the Indian Ocean L. longipes (Alcock & Anderson, 1899). The old records of the latter species from the Solomon Islands are now referred to the new species. The taxonomy of the other species is also discussed. Saint Laurent, 1989: Platyaxius Sakai, 1994; Albatrossaxius Sakai, 2011; Platyaxiopsis Sakai, 2011 and Newzealandaxius Sakai, 2011. Calaxius tungi Zhong, 2000 is synonymised with C. sibogae (De Man, 1925), Eiconaxius bandaensis Sakai, 2011 is synonymised with E. sibogae (De Man, 1925) and Tethisea mindoro Poore, 1997 is synonymised with T. indica Poore, 1994. Acanthaxius clevai Ngoc-Ho, 2006 is transferred to Pillsburyaxius, now Pillsburyaxius clevai (Ngoc-Ho, 2006), new combination.
???msg.biblio.biblioSurvey.label??? (27) [+] [-]BATHUS 1, BIOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 2, ???msg.security.private???, ???msg.security.private???, EBISCO, KARUBAR, KAVIENG 2014, LITHIST, MADEEP, MAINBAZA, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, PAPUA NIUGINI, SALOMON 1, SALOMONBOA 3, VOLSMAR, Walters Shoal
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Poppe G.T., Tagaro S.P. & Huang S.I. 2023. The recent Colloniidae with a study of the Colloniidae collected by various expeditions of the Muséum national 'Histoire naturelle, Paris. ConchBooks, Harxheim, Germany, 372 pp. ISBN:978-3-948603-36-6
???msg.biblio.biblioSurvey.label??? (40) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 2, BATHUS 3, BATHUS 4, BENTHEDI, BERYX 11, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, CHALCAL 1, CONCALIS, EBISCO, EXBODI, KARUBAR, KARUBENTHOS 2, KAVIENG 2014, LAGON, LIFOU 2000, LITHIST, MADEEP, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SMIB 8, TAIWAN 2000, TARASOC, ???msg.security.private???, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Richer de Forges B. & Ng P.K. 2020. The deep-water Homolidae of Papua New Guinea, (Crustacea: Decapoda: Brachyura), with description of a new species of Lamoha Ng, 1998, Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:239-258, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]Eight species of deep-water porter crabs of the family Homolidae are recorded from Papua New Guinea from three MNHN-led cruises to these waters: Homola orientalis Henderson, 1888, Homola coriolisi Guinot & Richer de Forges, 1995, Homolomannia sibogae Ihle, 1912, Homolomannia occlusa Guinot & Richer de Forges, 1981, Paromolopsis boasi Wood-Mason in Wood-Mason & Alcock, 1891, Lamoha woodmasoni n. sp., Ihlopsis multispinosa (Ihle, 1912) and Latreillopsis gracilipes Guinot & Richer de Forges, 1981. Most are new records for the country, Lamoha woodmasoni n. sp. appears to be the Pacific sister species of the Indian Ocean L. longipes (Alcock & Anderson, 1899). The old records of the latter species from the Solomon Islands are now referred to the new species. The taxonomy of the other species is also discussed.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rodríguez-Flores P.C., Macpherson E. & Machordom A. 2019. Revision of the squat lobsters of the genus Leiogalathea Baba, 1969 (Crustacea, Decapoda, Munidopsidae) with the description of 15 new species. Zootaxa 4560(2): 201-256. DOI:10.11646/zootaxa.4560.2.1
???msg.biblio.abstract.label??? [+] [-]The genus Leiogalathea Baba, 1969 currently contains only two benthic species both occurring on the continental shelves and slope: L. laevirostris (Balss, 1913), widely reported in the Indo-Pacific region, and L. agassizii (A. Milne Edwards, 1880), from both sides of the Central Atlantic. A certain degree of morphological variability linked to their geographic distributions was previously noticed, mostly in L. laevirostris. In the present study, we revise numerous specimens collected from the Atlantic, Indian and Pacific Oceans, analysing morphological and molecular characters (COI and 16S rRNA). We found 15 new species; all of them are distinguished from L. laevirostris and L. agassizii by subtle but constant morphological differences and show clear genetic separation. Furthermore, L. imperialis (Miyake & Baba, 1967), previously synonymized with L. laevirostris, was found to be a valid species. All species are described and illustrated. Species of the genus Leiogalathea are morphologically distinguishable on the basis of the spinulation of the carapace, the shape and the armature of the rostrum, the shape of the propodi of the walking legs, and the pattern of the setae covering on rostrum, carapace and chelae. Some species are barely discernible on the basis of these characters but are highly divergent genetically.
???msg.biblio.biblioSurvey.label??? (29) [+] [-]BATHUS 3, BERYX 11, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 2, CHALCAL 2, EBISCO, HALIPRO 2, KANACONO, KANADEEP, KARUBAR, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MUSORSTOM 4, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PAPUA NIUGINI, SALOMON 1, SANTO 2006, SMIB 3, SMIB 4, TARASOC, VOLSMAR
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rodríguez-Flores P.C., Seid C.A., Rouse G.W. & Giribet G. 2023. Cosmopolitan abyssal lineages? A systematic study of East Pacific deep-sea squat lobsters (Decapoda: Galatheoidea: Munidopsidae), in Ahyong S. (Ed.), Invertebrate Systematics 37(1): 14-60. DOI:10.1071/IS22030
???msg.biblio.abstract.label??? [+] [-]Munidopsid squat lobsters are among the most abundant decapods at abyssal depths and the most diverse squat lobster group in the East Pacific region. During recent cruises along the East Pacific, many deep-sea squat lobsters were collected. Among these, we described five new munidopsid species supported both by morphological characters and molecular phylogenetics: Munidopsis girguisi sp. nov., M. nautilus sp. nov., M. testuda sp. nov., M. cortesi sp. nov. and M. hendrickxi sp. nov. We also report new records of several Munidopsis species across the East Pacific that increase the species distribution ranges. Here, we reconstructed the phylogenetic relationships of the East Pacific species in relation to other Galatheoidea using one nuclear and two mitochondrial gene fragment(s); we also performed single locus species delimitation analyses to explore the species status of various East Pacific munidopsid taxa. The new taxa were photographed, illustrated and imaged with micro-computed tomography. The phylogenetic results show that: (1) Janetogalathea californiensis, previously included in the family Galatheidae, nests within Munidopsidae; (2) the phylogenetic position of Phylladiorhynchus and Coralliogalathea as belonging in Galatheidae is not supported; and (3) Munidopsis is paraphyletic, agreeing with recent systematic hypotheses. Short genetic distances and species delimitation analyses suggested that a clade mostly constituted by abyssal species might include fewer species than currently considered, as species show a wider geographic range than previously considered, conforming with traditional hypotheses of cosmopolitanisms in abyssal species.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]BIOMAGLO, GUYANE 2014, HALIPRO 2, KANACONO, KARUBAR, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MUSORSTOM 9, NORFOLK 2, TARASOC
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rodríguez‐Flores P.C., Buckley D., Macpherson E., Corbari L. & Machordom A. 2020. Deep‐sea squat lobster biogeography (Munidopsidae: Leiogalathea) unveils Tethyan vicariance and evolutionary patterns shared by shallow‐water relatives. Zoologica Scripta 49(3): 340-356. DOI:10.1111/zsc.12414
???msg.biblio.abstract.label??? [+] [-]The ecology, abundance and diversity of galatheoid squat lobsters make them an ideal group to study deep-sea diversification processes. Here, we reconstructed the evolutionary and biogeographic history of Leiogalathea, a genus of circum-tropical deep-sea squat lobsters, in order to compare patterns and processes that have affected shallow-water and deep-sea squat lobster species. We first built a multilocus phylogeny and a calibrated species tree with a relaxed clock using StarBEAST2 to reconstruct evolutionary relationships and divergence times among Leiogalathea species. We used BioGeoBEARS and a DEC model, implemented in RevBayes, to reconstruct ancestral distribution ranges and the biogeographic history of the genus. Our results showed that Leiogalathea is monophyletic and comprises four main lineages; morphological homogeneity is common within and between clades, except in one; the reconstructed ancestral range of the genus is in the Atlantic and Indian oceans (Tethys). They also revealed the divergence of the Atlantic species around 25 million years ago (Ma), intense cladogenesis 15–25 Ma and low levels of speciation over the last 5 million years (Myr). The four Leiogalathea lineages showed similar patterns of speciation: allopatric speciation followed by range expansion and subsequent stasis. Leiogalathea started diversifying during the Oligocene, likely in the Tethyan. The Atlantic lineage then split from its Indo-Pacific sister group due to vicariance driven by closure of the Tethys Seaway. The Atlantic lineage is less speciose compared with the Indo-Pacific lineages, with the Tropical Southwestern Pacific being the current centre of diversity. Leiogalathea diversification coincided with cladogenetic peaks in shallow-water genera, indicating that historical biogeographic events similarly shaped the diversification and distribution of both deep-sea and shallow-water squat lobsters.
???msg.biblio.biblioSurvey.label??? (34) [+] [-]BATHUS 3, BERYX 11, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 2, CHALCAL 2, ???msg.security.private???, EBISCO, EXBODI, HALIPRO 2, KANACONO, KANADEEP, KARUBAR, KARUBENTHOS 2, KAVIENG 2014, LAGON, MADEEP, MUSORSTOM 4, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SANTO 2006, SMIB 3, SMIB 4, ???msg.security.private???, TARASOC, VOLSMAR
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rubio F. & Rolán E. 2019. The genus Leucorhynchia Crosse, 1867 (Gastropoda, Skeneidae) in the Tropical Indo-Pacific. Museo de Historia Natural / Universidade de Santiago de Compostela, 287 pp. ISBN:978-84-8158-787-6
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, BATHUS 2, BATHUS 4, BENTHEDI, BIOPAPUA, EBISCO, EXBODI, INHACA 2011, KAVIENG 2014, LAGON, LIFOU 2000, MADEEP, MD32 (REUNION), MIRIKY, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 8, PANGLAO 2004, PAPUA NIUGINI, SALOMON 1, SANTO 2006, TARASOC, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Rubio F. & Rolán E. 2020. Conradiidae Golikov & Starobogatov, 1987 (= Crosseolidae Hickman, 2013) (Gastropoda, Trochoidea) from the Indo-Pacific. III. The genera Conradia and Conjectura. Novapex 21(2-3): 49-91
???msg.biblio.abstract.label??? [+] [-]This is the third contribution to the Indo-Pacific species of the family Conradiidae. In the present work 29 species of the genus Conradia A. Adams, 1860 and one species of the genus Conjectura Finlay, 1927 are studied, 20 of which are considered as new to science, and are described and figured. All these species are compared with the previously known species of these genera. The type material of Conradia carinifera A. Adams, 1860, Conradia cingulifera A. Adams, 1860, Conradia clathrata A. Adams, 1860, Conradia pulchella A. Adams, 1861, Conradia doliaris A. Adams, 1863, Conradia tornata A. Adams, 1863, Conradia (Gottoina) sulcifera A. Adams, 1863 and Conradia (Gottoina) pyrgula A. Adams, 1863 is illustrated for the first time.
???msg.biblio.biblioSurvey.label??? (15) [+] [-]BATHUS 1, BATHUS 2, BENTHEDI, BERYX 11, BOA0, BORDAU 1, EBISCO, MADEEP, MUSORSTOM 10, MUSORSTOM 3, MUSORSTOM 8, PANGLAO 2005, SALOMON 1, SALOMON 2, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Rubio F. & Rolán E. 2021. A review of Lyocyclidae Thiele, 1925 (Gastropoda: Caenogastropoda) from the Indo-Pacific, with the description of one new genus and twenty-eight new species. Iberus 39(1): 33-96. DOI:10.5281/zenodo.4969122
???msg.biblio.abstract.label??? [+] [-]Twenty-eight new upper-bathyal benthic species in Lyocyclidae (Caenogastropoda) from the Indo-Pacific are described, of which twenty-seven new species are assigned to the genus Lyocyclus Thiele, 1925 and one more in the new genus Nescitus n. gen, herein described. All species are illustrated by SEM micrographs and compared with the previously known ones. Photographs of the species described by THIELE (1925) from the Indian Ocean are provided for the first time. Lyocyclus biconcavus Thiele, 1925 is here assigned to the genus Eudaronia Cotton, 1945 and Lyocyclus orientalis Thiele, 1925 to the genus Adeuomphalus Seguenza, 1876, both in the Seguenzioidea superfamily.
???msg.biblio.biblioSurvey.label??? (16) [+] [-]BATHUS 1, BATHUS 2, BIOGEOCAL, BIOPAPUA, BORDAU 1, EXBODI, KAVIENG 2014, MADEEP, MAINBAZA, MUSORSTOM 10, MUSORSTOM 8, NORFOLK 2, SALOMON 1, SALOMON 2, SMIB 8, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Rubio F. & Rolán E. 2022. New species of Vitrinellidae (Gastropoda: Truncatelloidea) from the Indo-Pacific. The genus Circulus Jeffreys, 1865. Museo Nacional de Historia Natural, Universidad de Santiago de Compostela. Museo National de Historia Natural, Universidad de Santiago de Compostela, 422 pp. ISBN:978-84-09-41918-0
???msg.biblio.biblioSurvey.label??? (48) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 4, BENTHAUS, BENTHEDI, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BORDAU 1, BORDAU 2, CORAIL 2, CORINDON 2, EBISCO, EXBODI, INHACA 2011, KANACONO, KARUBAR, KAVIENG 2014, LAGON, LIFOU 2000, MADEEP, MAINBAZA, MD32 (REUNION), MIRIKY, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, ???msg.security.private???, ???msg.security.private???, TAIWAN 2002, TARASOC, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Samadi S., Puillandre N., Pante E., Boisselier M.C., Corbari L., Chen W.J., Maestrati P., Mana R., Thubaut J., Zuccon D. & Hourdez S. 2015. Patchiness of deep‐sea communities in Papua New Guinea and potential susceptibility to anthropogenic disturbances illustrated by seep organisms. Marine Ecology 36(S1): 109-132. DOI:10.1111/maec.12204
???msg.biblio.abstract.label??? [+] [-]The deep-sea part of the ‘Papua Niugini Biodiversity Expedition’ surveyed the deep-sea environments along the coasts of New Guinea Island in the Bismarck Sea, from the Vitiaz Strait to the border between Papua New Guinea (PNG) and Irian Jaya. This expedition was a follow-up of the BIOPAPUA cruise (2010) that gave some of the first insights into the diversity of the deep-sea fauna of the Bismarck and Solomon Seas for environments other than deep-sea hydrothermal vents. The main aims of the cruise were to survey the diversity of the fauna of (i) hard bottoms that are typically found on deep seamounts, (ii) Astrolabe Bay from 200 m to about 1000 m, (iii) the chemosynthetic environments of the deep sea, including cold-seep environments and plant debris. Astrolabe Bay was one of our targets because its topography allows sampling over the complete bathymetric gradient covered by our sampling gear (down to 1000 m depth), and the recent start of nickel refining activities in the bay is a potential threat to its marine fauna for which little reference data are available. Sampling in the bay revealed not only a diversified fauna associated with soft bottoms and plant debris, but also a chemosynthetic fauna typical of coldseep environments (e.g. siboglinid worms and bathymodioline mussels) below the Ramu refinery. Although the refinery activities had officially started just one week before our work in the area, we observed impacts of these activities. Our molecular work indicates that the siboglinid tubeworm species and one of the two mussel species collected below the Ramu refinery have so far only been documented from this location, despite intensive sampling effort. This illustrates the potential destructive effects of human activities in areas where the diversity and uniqueness of deep-sea communities are poorly understood.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IA (Annélides, Polychètes et Sipunculides) -
Siegwald J., Oskars T.R., Kano Y. & Malaquias M.A.E. 2022. A global phylogeny of the deep-sea gastropod family Scaphandridae (Heterobranchia: Cephalaspidea): Redefinition and generic classification. Molecular Phylogenetics and Evolution 169: 107415. DOI:10.1016/j.ympev.2022.107415
???msg.biblio.abstract.label??? [+] [-]We present the most comprehensive phylogeny of a globally distributed deep-sea group of gastropods published to date including over 80% of the recognized diversity of the family Scaphandridae. The definition and taxo nomic composition of the Scaphandridae has been hampered by the lack of a sound phylogenetic framework and definition of synapomorphic traits. We used a combination of molecular phylogenetics (Bayesian Inference and Maximum Likelihood) based on five gene markers (cytochrome c oxidase subunit I, 12S rRNA, 16S rRNA, 18S rRNA, and 28S rRNA) and morpho-anatomical characters to redefine the Scaphandridae and its genera. A new classification is proposed with the three genera Nipponoscaphander, Sabatia, and Scaphander. Main differences between genera lie on the shells (shape, parietal callus, spire) and male reproductive system (prostate). The species Hamineobulla kawamurai is reassigned to the closely related family Eoscaphandridae, currently defined mostly based on pleisiomorphic traits. Biogeographically the genus Nipponoscaphander is restricted to the IndoWest Pacific; Sabatia is mostly circumscribed to the Indo-West Pacific, but has one lineage present in the north Atlantic Ocean. Polyphyly across ocean realms prevails in the specious and globally distributed genus Scaphander with multiple speciation events between Indo-Pacific and Atlantic lineages but also with several episodes of cladogenesis within realms. Two rare cases of species with a broad distribution spanning the Indo-West Pacific and Atlantic realms are confirmed (S. meridionalis and S. nobilis)
???msg.biblio.biblioSurvey.label??? (17) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MAINBAZA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, TARASOC, Walters Shoal
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Summers N. & Watling L. 2021. Upper Bathyal Pacific Ocean biogeographic provinces from octocoral distributions. Progress in Oceanography 191: 102509. DOI:10.1016/j.pocean.2020.102509
???msg.biblio.abstract.label??? [+] [-]Biogeographical classification schemes such as the Marine Ecoregions of the World (MEOW) have been devel oped for continental shelf depths. The lack of faunal data in the deep sea has led to the development of biogeographical units based on oceanographic characteristics. The aim of this study was to propose biogeo graphical schemes for the Upper Bathyal (200–1000 m) across the Pacific Ocean using octocoral distributions. We retrieved over 200 000 octocoral data records from the Deep Sea Coral Data Portal (DSCDP), Ocean Biogeographic Information System (OBIS), Tropical Deep-Sea Benthos program (French National Museum of Natural History), Queensland Museum from the CIDARIS expeditions, and records retrieved from the Siboga expedition reports. We used cluster analysis to examine octocoral distributions against four different biogeo graphical classification schemes. The classification schemes produced mostly concordant patterns with three major faunal distribution barriers: the North Pacific Current isolates the subarctic units by creating a steep temperature gradient; the Subantarctic Front separates the Subantarctic from the rest of the Pacific; and the East Pacific Barrier separates the East Pacific from the Central and West Pacific. Two other smaller but distinct provinces are the Indo-Pacific where Lower Bathyal genera are found in the Upper Bathyal, and Torres Strait/ Coral Sea characterised by mesophotic genera. We propose 12 biogeographic provinces across the Pacific Ocean Upper Bathyal region from 200 to 1000 m depth based on octocoral distributions. The main driver for these units seems to be temperature, a defining feature of water masses. These units could potentially be subdivided into smaller regions based on habitat. Additionally, the clustering of Ecological Marine Units (EMUs) provides evi dence that the Upper Bathyal should in certain regions be divided vertically into two depth zones based on water masses.
???msg.biblio.biblioSurvey.label??? (9) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Suárez-Morales E. & Salazar-Vallejo S.I. 2025. Expanding territories: new host records and four new species of herpyllobiid parasitic copepods (Copepoda: Herpyllobiidae) from Papua New Guinea deep-water polynoid polychaetes (Annelida: Polynoidae). Journal of Natural History 59(13-16): 1017-1047. DOI:10.1080/00222933.2025.2474196
???msg.biblio.abstract.label??? [+] [-]The parasitological examination of polynoid polychaetes collected in deep water substrates (333–780 m) off Papua New Guinea allowed us to detect four infected specimens, including two new annelid host species (Harmothoe samadiae sp. n., Eunoe corbariae sp. n.), Lepidasthenia brunnea sensu Knox, and Harmothoe sp. Three of the parasites were identified as members of the mesoparasitic copepod genus Herpyllobius Steenstrup and Lütken, and one of Gottoniella López-González, Bresciani and Conradi, (Herpyllobiidae). Herpyllobius chambardi sp. n., found on L. brunnea, is distinguished from its con generic species by having a longitudinal constriction dividing its glo bose ectosoma into two symmetrical hemispheres. The second species, H. hourdezi sp. n., on H. samadiae, shows a depressed intergenital margin, lacks sclerotised dots, and exhibits a large endosoma with several thick lobes. Herpyllobius pabloi sp. n., found on E. corbariae, closely resembles its congeneric species H. polynoes, but differs in the endosomal structure and details of the ectosoma. Herpyllobius species are known to infect at least 14 polynoid genera, to which we can now add Lepidasthenia Malmgren, thus expanding its host range among polynoids. These three Papuan species are additional new records of this chiefly cold-temperate copepod genus to be reported from sub tropical latitudes. The discovery of Herpyllobius parasitising a species of Harmothoe confirms its preference for infecting this polynoid genus. The new Gottoniella, also on Harmothoe sp. is the third known species of the genus; it has heavily sclerotised genital swellings, slit-like genital openings, a distinctive fin-like lateral ectosomal process, a short, sclero tised ring, and a pipe-like stalk connecting the endosoma. Both H. chambardi and H. hourdezi are among the deep-living members of Herpyllobius in the Southern Hemisphere, the latter representing the deepest record of the genus (780 m) worldwide.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IA (Annélides, Polychètes et Sipunculides), IU (Crustacés) -
TAYLOR J.D., GLOVER E.A., Yuen B. & Williams S.T. 2022. Closing the gap: a new phylogeny and classification of the chemosymbiotic bivalve family Lucinidae with molecular evidence for 73% of living genera. Journal of Molluscan Studies 88(4): eyac025. DOI:10.1093/mollus/eyac025
???msg.biblio.abstract.label??? [+] [-]New molecular phylogenies of the chemosymbiotic bivalve family Lucinidae, using 18S rRNA, 28S rRNA and cytochrome b genes, include species from genera not previously analysed. Notable additions from Myrteinae are sequences from Rostrilucina, Solelucina and Taylorina species, species of Ustalucina, Gonimyrtea from Leucosphaerinae and additional species of Ctena, Codakia, Lucinoma and Divalucina from Codakiinae. New sequences of Lucininae include the type species of Parvilucina (P. tenuisculpta), Liralucina, Falsolucinoma, Easmithia, Jallenia, Radiolucina and Cardiolucina as well as samples of Loripes orbiculatus from multiple localities. Five major clades, defined as subfamilies, are recognized: Pegophyseminae, Myrteinae, Leucosphaerinae, Codakiinae and Lucininae. Two branches, Fimbriinae and Monitilorinae, are represented by single species. Pegophyseminae are an extremely long-branched group with a sister-group relationship to Leucosphaerinae, while Codakiinae are a sister clade to the Lucininae. In various gene trees, the position of Myrteinae is unstable in relation to Pegophyseminae + Leucosphaerinae, Monitilorinae and Fimbriinae. The Myrteinae are not well resolved, with an ambiguous correlation of molecular and morphological characters. Codakiinae now include Divalucina cumingi, shown to be related to Lucinoma rather than Divaricella and Divalinga of the Lucininae. Leucosphaerinae are a well-supported clade but morphologically disparate, with the positions of Gonimyrtea and Callucina unresolved. Several molecularly distinct subclades are recognized within the Lucininae, especially the Lucinisca, Loripes and Parvilucina groups. Parvilucina species are paraphyletic with P. tenuisculpta, the type species, distinct from the western Atlantic species. Codakia, Ctena and Pegophysema have pan-tropical distributions with former connections disrupted by vicariant events of the closure of the eastern Tethyan and Central American Seaways. Species of Radiolucina, Pleurolucina and Lucinisca are present on either side of the Isthmus of Panama. A new classification of the 96 living lucinid genera is presented, providing a framework for future studies of systematics, ecology, biogeography and bacterial symbioses.
???msg.biblio.biblioSurvey.label??? (24) [+] [-]ATIMO VATAE, BIOPAPUA, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, ILES DU SALUT, INHACA 2011, KARUBAR, KARUBENTHOS 2012, KAVIENG 2014, KOUMAC 2.3, LAGON, MADEEP, MIRIKY, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Taylor J.D., Glover E.A., Smith L., Ikebe C. & Williams S.T. 2016. New molecular phylogeny of Lucinidae: increased taxon base with focus on tropical Western Atlantic species (Mollusca: Bivalvia). Zootaxa 4196(3): 381-398. DOI:10.11646/zootaxa.4196.3.2
???msg.biblio.abstract.label??? [+] [-]A new molecular phylogeny of the Lucinidae using 18S and 28S rRNA and cytochrome b genes includes many species from the tropical Western Atlantic as well as additional taxa from the Indo-West Pacific. This study provides a phylogenetic framework for a new taxonomy of tropical Western Atlantic lucinids. The analysis confirmed five major clades—Pegophyseminae, Leucosphaerinae, Myrteinae, Codakiinae and Lucininae, with Monitilorinae and Fimbriinae represented by single species. The Leucosphaerinae are expanded and include Callucina winckworthi and the W. Atlantic Myrtina pristiphora that groups with several Indo-West Pacific Myrtina species. Within the Codakiinae two abundant species of Ctena from the Western Atlantic with similar shells are discriminated as C. orbiculata and C. imbricatula, while in the Indo-West Pacific Ctena bella is a probable species complex. The Lucininae is the most species rich and disparate subfamily with several subclades apparent. Three species of Lucina are recognized in the W. Atlantic L. aurantia, L. pensylvanica and L. roquesana. Pleurolucina groups near to Cavilinga and Lucina, while Lucinisca muricata is more closely related to the E. Pacific L. fenestrata than to the Atlantic L. nassula. A new species of Parvilucina is identified from molecular analyses having been confounded with Parvilucina pectinata but differs in ligament structure. Also, the former Parvilucina clenchi is more distant and assigned to Guyanella.
???msg.biblio.biblioSurvey.label??? (10) [+] [-]ATIMO VATAE, BIOPAPUA, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, MADEEP, PANGLAO 2004, PAPUA NIUGINI
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Tongboonkua P., Lee M.Y. & Chen W.J. 2018. A new species of sinistral flatfish of the genus Chascanopsetta (Teleostei: Bothidae) from off Papua New Guinea, western Pacific Ocean. Zootaxa 4476(1): 168. DOI:10.11646/zootaxa.4476.1.16
???msg.biblio.abstract.label??? [+] [-]Left-eyed flounders of the genus Chascanopsetta Alcock 1894 (Bothidae) occur in the Indian, Pacific, and Atlantic oceans at depths ranging from 120 to 1500 meters. They possess some unique features in bothid fishes including a strongly compressed and elongated body and a tremendously large mouth. Currently, nine species of Chascanopsetta are recognized, and three of them (C. micrognatha Amaoka & Yamamoto 1984, C. lugubris Alcock 1894 and C. prognatha Norman 1939) are distributed in the West Pacific. We collected 25 specimens of Chascanopsetta during 11 biodiversity expeditions carried out mainly in the West Pacific. Among them, eight specimens taken off Papua New Guinea present morphological features that differ from those of the three nominal species known in the West Pacific. In this study, we examined these eight specimens of unknown affinity and compared their morphology to that of specimens of other congeneric species. Results of these comparisons showed that these specimens represent an undescribed species of Chascanopsetta, named herein, C. novaeguineae sp. nov.. The new species resembles C. elski Foroshchuk 1991, which is known only from the Saya de Malha Bank in the western Indian Ocean, in having a high number of gill rakers (> 13). However, the combination of the following characters further distinguishes C. novaeguineae sp. nov. from C. elski: longer jaws, narrower interorbital width, and number of pseudobranches (21–25 vs. 26–27). The DNA sequences from the mitochondrial cytochrome oxidase subunit I (COI) gene from C. novaeguineae sp. nov. and other species were obtained and compared to confirm its taxonomic status and to infer its tentative phylogenetic position within the Chascanopsetta.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]AURORA 2007, BIOPAPUA, DongSha 2014, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, MADEEP, NanHai 2014, SALOMONBOA 3, ZhongSha 2015
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Vilvens C. 2024. New species and new records of Calliostomatidae (Gastropoda: Trochoidea) from western Pacific (II): Solomon Islands, Papua New Guinea, Indonesia, Philippines and Taiwan. Novapex 25(2): 55-110
???msg.biblio.biblioSurvey.label??? (21) [+] [-]BIOPAPUA, CORINDON 2, EBISCO, KARUBAR, KAVALAN 2018, KAVIENG 2014, MADEEP, MUSORSTOM 3, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, TAIWAN 2000, TAIWAN 2001, TAIWAN 2002, TAIWAN 2004, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Wang S.Y., Chen J.N., Russell B.C. & Chen W.J. 2018. First record of Gauguin's blunt-nose lizardfish, Trachinocephalus gauguini Polanco, Acero & Betancur 2016 (Teleostei: Synodontidae) outside the Marquesas Archipelago. Zootaxa 4476(1): 151-156. DOI:10.11646/zootaxa.4476.1.14
???msg.biblio.abstract.label??? [+] [-]Trachinocephalus gauguini Polanco, Acero & Betancur, 2016 was described based on eighteen specimens collected from off the Marquesas Islands, the only location where this species has been recorded until now. Through morphological and molecular examination of Trachinocephalus specimens collected from an exploratory cruise conducted in June 2014 under the Tropical Deep-Sea Benthos program along the northern coast of the New Ireland Province, Papua New Guinea, we demonstrate the presence of this species in Papua New Guinea waters. This new record suggests a wide distribution for this rarely collected species in the western Pacific Ocean.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
White O.W., Hall A., Price B.W., Williams S.T. & Clark M.D. 2025. A Snakemake Toolkit for the Batch Assembly, Annotation and Phylogenetic Analysis of Mitochondrial Genomes and Ribosomal Genes From Genome Skims of Museum Collections. Molecular Ecology Resources 25(1): e14036. DOI:10.1111/1755-0998.14036
???msg.biblio.abstract.label??? [+] [-]Low coverage ‘genome-skims’ are often used to assemble organelle genomes and ribosomal gene sequences for cost-effective phylogenetic and barcoding studies. Natural history collections hold invaluable biological information, yet poor preservation resulting in degraded DNA often hinders polymerase chain reaction-based analyses. However, it is possible to generate libraries and sequence the short fragments typical of degraded DNA to generate genome-skims from museum collections. Here we introduce a snakemake toolkit comprised of three pipelines skim2mito, skim2rrna and gene2phylo, designed to unlock the genomic potential of historical museum specimens using genome skimming. Specifically, skim2mito and skim2rrna perform the batch assembly, annotation and phylogenetic analysis of mitochondrial genomes and nuclear ribosomal genes, respectively, from low-coverage genome skims. The third pipeline gene2phylo takes a set of gene alignments and performs phylogenetic analysis of individual genes, partitioned analysis of concatenated alignments and a phylogenetic analysis based on gene trees. We benchmark our pipelines with simulated data, followed by testing with a novel genome skimming dataset from both recent and historical solariellid gastropod samples. We show that the toolkit can recover mitochondrial and ribosomal genes from poorly preserved museum specimens of the gastropod family Solariellidae, and the phylogenetic analysis is consistent with our current understanding of taxonomic relationships. The generation of bioinformatic pipelines that facilitate processing large quantities of sequence data from the vast repository of specimens held in natural history museum collections will greatly aid species discovery and exploration of biodiversity over time, ultimately aiding conservation efforts in the face of a changing planet.
???msg.biblio.biblioSurvey.label??? (7) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
White W.T., Mana R.R. & Naylor G.J. 2016. Galeus corriganae sp. nov., a new species of deepwater catshark (Carcharhiniformes: Pentanchidae) from Papua New Guinea. Zootaxa 4205(3): 255-264. DOI:10.11646/zootaxa.4205.3.5
???msg.biblio.abstract.label??? [+] [-]A new species of catshark, provisionally placed in the genus Galeus, is described from Papua New Guinea based on 7 specimens collected during recent deepwater surveys of the region. The new species, Galeus corriganae, is closest to G. priapus from New Caledonia and G. gracilis from northwestern Australia but differs in several morphological characters. A reclassification of the catshark groups is required to revise the familial and generic arrangement of the group.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
White W.T., Mana R.R. & Naylor G.J. 2017. Description of a new species of deepwater catshark Apristurus yangi n.sp (Carcharhiniformes: Pentanchidae) from Papua New Guinea. Zootaxa 4320(1): 25-40. DOI:10.11646/zootaxa.4320.1.2
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
White W.T. & Ko’Ou A. 2018. An annotated checklist of the chondrichthyans of Papua New Guinea. Zootaxa 4411(1): 001-082. DOI:10.11646/zootaxa.4411.1.1
???msg.biblio.abstract.label??? [+] [-]An annotated checklist of the chondrichthyan fishes (sharks, rays, and chimaeras) of Papua New Guinean waters is herein presented. The checklist is the result of a large biodiversity study on the chondrichthyan fauna of Papua New Guinea between 2013 and 2017. The chondrichthyan fauna of Papua New Guinea has historically been very poorly known due to a lack of baseline information and limited deepwater exploration. A total of 131 species, comprising 36 families and 68 genera, were recorded. The most speciose families are the Carcharhinidae with 29 species and the Dasyatidae with 23 species. Verified voucher material from various biological collections around the world are provided, with a total of 687 lots recorded comprising 574 whole specimens, 128 sets of jaws and 21 sawfish rostra. This represents the first detailed, verified checklist of chondrichthyans from Papua New Guinean waters.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Wong M.K., Lee M.Y. & Chen W.J. 2021. Integrative taxonomy reveals a rare and new cusk-eel species of Luciobrotula (Teleostei, Ophidiidae) from the Solomon Sea, West Pacific. European Journal of Taxonomy 750: 52-69. DOI:10.5852/ejt.2021.750.1361
???msg.biblio.abstract.label??? [+] [-]With six valid species, Luciobrotula is a small genus of the family Ophidiidae, commonly known as cusk-eels. They are benthopelagic fishes occurring at depths ranging from 115–2300 m in the Atlantic, Indian, and Pacific Oceans. Among them, Luciobrotula bartschi is the only known species in the West Pacific. Three specimens of Luciobrotula were collected from the Philippine Sea, Bismarck Sea, and Solomon Sea in the West Pacific during the AURORA, PAPUA NIUGINI, and MADEEP expeditions under the Tropical Deep-Sea Benthos program, and all of them were initially identified as L. bartschi. Subsequent examination with integrative taxonomy indicates that they belong to two distinct species, with the specimen collected from the Solomon Sea representing a new species, which is described here. In terms of morphology, Luciobrotula polylepis sp. nov. differs from its congeners by having a relatively longer lateral line (end of the lateral line below the 33rd dorsal-fin ray) and fewer vertebrae (abdominal vertebrae 13, total vertebrae 50). In the inferred COI gene tree, the two western Pacific species of Luciobrotula do not form a monophyletic group. The genetic K2P distance between the two species is 13.8% on average at the COI locus.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Wong M.K. & Chen W.J. 2024. Exploring the phylogeny and depth evolution of cusk eels and their relatives (Ophidiiformes: Ophidioidei). Molecular Phylogenetics and Evolution 199: 108164. DOI:10.1016/j.ympev.2024.108164
???msg.biblio.abstract.label??? [+] [-]With 289 known species in 51 genera, the ophidiiform family Ophidiidae together with their relatives from the Carapidae (36 species in eight genera) of the same suborder Ophidioidei dominate the deep sea, but some occur also in shallow water habitats. Despite their high species diversity in the deep sea and wide bathymetric distributions, their phylogenetic relationships and evolution remain unexplored due in part to sampling difficulties. Thanks to the biodiversity exploratory program entitled “Tropical Deep-Sea Benthos” and joint efforts between Taiwan and French teams for sampling from different localities across the Indo-West Pacific over the last two decades, we are able to compile comprehensive datasets for investigations. In this study, 59 samples representing 36 of 59 known ophidioid genera are selected and used to construct a multi-gene dataset to infer the phylogenetic relationships of ophidioid fishes and their relatives. Our results reveal that the Ophidiidae forms a paraphyletic group with respect to the Carapidae. The four main clades of Ophidioidei resolved are the (1) clade comprising species from the subfamily Brotulinae; (2) clade that includes species in the genera Acanthonus and Xyelacyba; (3) clade grouping Hypopleuron caninum with species from the family Carapidae; and (4) clade containing the species in the subfamily Brotulotaenilinae, Neobythitinae (in part), and Ophidiinae. Accordingly, we suggest the following new revisions based on our results and proposed morphological diagnoses. The subfamily Brotulinae should be elevated to the family level. The genera Xyelacyba and probably Tauredophidium (unsampled in this study) should be included in the newly established family Acanthonidae with Acanthonus. The families Carapidae and Ophidiidae are re-defined. Our time-calibrated phylogenetic and ancestral depth reconstructions enable us to clarify the evolutionary history of ophidiiform fishes and infer past patterns of species distributions at different depths. While Ophidiiformes is inferred to have originated in shallow waters around 96.25 million years ago (Mya), the common ancestor to the Ophidioidei is inferred to have invaded the deep sea around 90.22 Mya, the dates coinciding with the global anoxic event of the OAE2. The observed bathymetric distribution patterns in Ophidioidei most likely point to the mesopelagic zone as the center of origin and diversification. This was followed by multiple events of depth transitions or range expansions towards either shallower waters or greater depth zones, which were likely triggered by past climate changes during the Paleogene-Neogene.
???msg.biblio.biblioSurvey.label??? (19) [+] [-]AURORA 2007, BIOMAGLO, BIOPAPUA, DongSha 2014, EXBODI, KANACONO, KANADEEP, KANADEEP 2, KAVIENG 2014, MADEEP, NanHai 2014, ???msg.security.private???, PAPUA NIUGINI, SAKIZAYA 2019, SAYA, SPANBIOS, TAIWAN 2013, TARASOC, ZhongSha 2015
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Yang C.H., Chan T.Y. & Kumar A.B. 2018. The deep-sea commercial caridean shrimp, Heterocarpus woodmasoni (Crustacea: Decapoda: Panalidae), with description of a new species from the western Pacific Ocean. Bulletin of Marine Science 94(1): 85-99. DOI:10.5343/bms.2017.1119
???msg.biblio.abstract.label??? [+] [-]The availability of fresh specimens of the commercial, deep-sea pandalid shrimp, Heterocarpus woodmasoni Alcock, 1901, from India revealed that material referred to this species from India and the western Pacific Ocean have distinct differences in coloration, morphology, and genetic divergence. Although the syntypes of H. woodmasoni cannot be located now, a color photograph of a typotypic specimen from the Andaman Sea allowed the determination of the Indian form as the true H. woodmasoni. To stabilize the taxonomy in the “H. woodmasoni” species group, a neotype is selected for H. woodmasoni from an Indian specimen with both coloration and molecular barcoding information. The western Pacific form is described as a new species, Heterocarpus fascirostratus sp. nov., which differs from H. woodmasoni in having a banded rostrum, eggs reddish brown instead of greenish brown, lacking rostral crest, armed usually with fewer dorsolateral spines on the telson, the overhanging spine on the abdominal somite III not markedly recurved downwards, and a rather straight postantennal carina.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Zaharias P., Kantor Y.I., Fedosov A.E., Criscione F., Hallan A., Kano Y., Bardin J. & Puillandre N. 2020. Just the once will not hurt: DNA suggests species lumping over two oceans in deep-sea snails (Cryptogemma). Zoological Journal of the Linnean Society 190(2): 532-557. DOI:10.1093/zoolinnean/zlaa010
???msg.biblio.abstract.label??? [+] [-]Abstract The practice of species delimitation using molecular data commonly leads to the revealing of species complexes and an increase in the number of delimited species. In a few instances, however, DNA-based taxonomy has led to lumping together of previously described species. Here, we delimit species in the genus Cryptogemma (Gastropoda: Conoidea: Turridae), a group of deep-sea snails with a wide geographical distribution, primarily by using the mitochondrial COI gene. Three approaches of species delimitation (ABGD, mPTP and GMYC) were applied to define species partitions. All approaches resulted in eight species. According to previous taxonomic studies and shell morphology, 23 available names potentially apply to the eight Cryptogemma species that were recognized herein. Shell morphometrics, radular characters and geographical and bathymetric distributions were used to link type specimens to these delimited species. In all, 23 of these available names are here attributed to seven species, resulting in 16 synonymizations, and one species is described as new: Cryptogemma powelli sp. nov. We discuss the possible reasons underlying the apparent overdescription of species within Cryptogemma, which is shown here to constitute a rare case of DNA-based species lumping in the hyper-diversified superfamily Conoidea.
???msg.biblio.biblioSurvey.label??? (25) [+] [-]ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, CONCALIS, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PANGLAO 2004, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, TAIWAN 2013, TARASOC, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Zaharias P., Kantor Y.I., Fedosov A.E. & Puillandre N. 2024. Coupling DNA barcodes and exon-capture to resolve the phylogeny of Turridae (Gastropoda, Conoidea). Molecular Phylogenetics and Evolution 191: 107969. DOI:10.1016/j.ympev.2023.107969
???msg.biblio.biblioSurvey.label??? (38) [+] [-]ATIMO VATAE, AURORA 2007, BIOMAGLO, BIOPAPUA, BOA1, CONCALIS, CORSICABENTHOS 1, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KANACONO, KANADEEP, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, MAINBAZA, MIRIKY, MUSORSTOM 9, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2004, TAIWAN 2013, TARASOC, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Zhang R., Fau M., Mah C., Eléaume M., Zhang D., Zhou Y., Lu B. & Wang C. 2024. Systematics of deep-sea starfish order Brisingida (Echinodermata: Asteroidea), with a revised classification and assessments of morphological characters. Molecular Phylogenetics and Evolution 191: 107993. DOI:10.1016/j.ympev.2023.107993
???msg.biblio.biblioSurvey.label??? (58) [+] [-]???msg.security.private???, ANT-XXIX_3, ATIMO VATAE, BATHUS 2, BATHUS 4, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, BENTHAUS, ???msg.security.private???, BIOCAL, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, BIOGEOCAL, BIOMAGLO, BIOPAPUA, ???msg.security.private???, CEAMARC-AA, CHALCAL 2, CONCALIS, CORINDON 2, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, EBISCO, EXBODI, HALIPRO 2, ???msg.security.private???, 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, ???msg.security.private???, NORFOLK 2, NanHai 2014, ???msg.security.private???, SALOMON 1, SALOMON 2, SALOMONBOA 3, SPANBIOS, TAIWAN 2000, ???msg.security.private???, TARASOC, ???msg.security.private???, Walters Shoal, ZhongSha 2015
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
ĎUriš Z. & Šobáňová A. 2020. Deep sea palaemonid shrimps of Papua New Guinea (Crustacea: Decapoda: Palaemonidae), Deep-Sea Crustaceans from Papua New Guinea - Tropical Deep-Sea Benthos 31. Mémoires du Muséum national d'histoire naturelle Tome 213. Publications scientifiques du Muséum national d'histoire naturelle, Paris:369-402, ISBN:978-2-85653-913-2
???msg.biblio.abstract.label??? [+] [-]Material collected during the expeditions BIOPAPUA 2010, PAPUA NIUGINI 2012, MADEEP 2014, and KAVIENG 2014, in the waters of the Bismarck and Solomon Seas of Papua New Guinea (PNG) yielded 12 species of deep-sea shrimps of the family Palaemonidae. Besides one new species of the genus Amphipontonia described in this paper, seven others, namely Bathymenes aleator, Echinopericlimenes calcaratus, Palaemonella dolichodactylus, P. komaii, P. spinulata, Periclimenes laccadivensis, and P. uniunguiculatus, are new records for Papua New Guinea. An extension to the known bathymetric range is reported here for the deep-water species Palaemonella dolichodactylus, P. komaii, P. spinulata, and Periclimenes uniunguiculatus, and also for two species previously considered as restricted to shallow water, i.e., Laomenes amboinensis and Ancylomenes sp., collected from depths over 90 and 180 m, respectively. Based on the present molecular analysis and additional GenBank sequences, three deep-water Periclimenes species, i.e., P. boucheti, P. leptunguis, and P. sandybrucei, are formally transferred here to the genus Bathymenes, and B. brevirostris is synonymized with B. aleator.
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés)
???msg.campaign.menu.documents???
- Documents logistiques
- ???msg.connection.private.label??? (1)
- Dossier(s) de préparation de mission
- Demande de campagne - Flotte océanographique Française 2014
- ???msg.connection.private.label??? (1)
- Rapport(s) de mission
- Compte-rendu de la campagne
- Rapport scientifique de la campagne
???msg.campaign.menu.photos???
Collecte : 572 photos
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Organisme : 948 photos
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Substrat : 16 photos
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Débris organiques : 193 photos
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Détritus : 25 photos
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Sur le pont : 22 photos
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???msg.campaign.menu.participants???
???msg.field.stage.byLabel??? :
- Leg 1 (Sun Apr 06 00:00:00 UTC 2014 - Fri Apr 18 00:00:00 UTC 2014) ???msg.table.stage.ship.label??? : Alis
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- Corbari, Laure (Carcinologie, Muséum national d'Histoire naturelle)
- Chef de mission
- Mana, Ralph ( University of Papua New Guinea)
- Observateur
- Olu‐Le Roy, Karine (Ecologie des environnements chimiosynthétiques, Institut Français de Recherche pour l'Exploitation de la Mer)
- Chef de mission
- Quinquis, Renaud ( Genavir)
- Opérateur Scampi
- Sen, Arunima (Analyse d’images sous SIG, Institut Français de Recherche pour l'Exploitation de la Mer)
- Analyse SIG
- Tranvouez, Simon ( Genavir)
- Opérateur Scampi
- Leg 2 (Sun Apr 20 00:00:00 UTC 2014 - Thu May 08 00:00:00 UTC 2014) ???msg.table.stage.ship.label??? : Alis
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- Chambard, Cyril ( Muséum national d'Histoire naturelle)
- Collecte - Tri
- Chen, Janet (Ichtyologie, National Taiwan University, Institute Of Oceanography)
- Collecte - Tri
- Corbari, Laure (Carcinologie, Muséum national d'Histoire naturelle)
- Chef de mission
- Ganzik, Ken ( University of Papua New Guinea)
- Collecte - Tri
- Hourdez, Stéphane (Systématique des annélides, Centre National de la Recherche Scientifique)
- Collecte - Tri
- Samadi, Sarah (Biologie évolutive, Muséum national d'Histoire naturelle)
- Chef de mission
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???msg.campaign.download.kml???
???msg.campaign.menu.stations???
???msg.campaign.menu.taxons???
| ???msg.field.class.label??? | ???msg.security.label??? | ???msg.table.taxons.count.label??? |
|---|---|---|
| Asteroidea | ???msg.security.public??? | 1 |
