161 ???count.stations.label???
EXBODI
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- MNHN - Muséum national d'Histoire naturelle
- IRD - Institut de Recherche pour le Développement
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- Samadi Sarah (Leg 1)
- Corbari Laure (Leg 2)
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Fri Sep 02 00:00:00 UTC 2011 Port-Vila (Vanuatu)???msg.table.location.campaign.stop.label???
Wed Sep 28 00:00:00 UTC 2011 Nouméa (Nouvelle-Calédonie)| ???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 | Fri Sep 02 00:00:00 UTC 2011 | Sun Sep 11 00:00:00 UTC 2011 | Nouméa (Nouvelle-Calédonie) | Nouméa (Nouvelle-Calédonie) | Alis |
| Leg 2 | Mon Sep 12 00:00:00 UTC 2011 | Thu Sep 29 00:00:00 UTC 2011 | Nouméa (Nouvelle-Calédonie) | Nouméa (Nouvelle-Calédonie) | Alis |
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La campagne EXBODI, initialement prévue au Vanuatu, s'est finalement déroulée en Nouvelle-Calédonie. Les objectifs étaient de complèter les échantillonages dans les eaux néo-calédoniennes ainsi que d'étudier la biologie et la diversité des organismes associés aux bois coulés. ???msg.campaign.readMore???
???msg.campaign.menu.info.works??? :
161 opérations ont été réalisées dont 71 traits de chalut à perche et 90 dragages à la drague Warèn.
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???msg.campaign.menu.bibliographies??? (124) [+] [-]
???msg.biblio.toExportPage.label???
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Abdelkrim J., Aznar-Cormano L., Fedosov A.E., Kantor Y.I., Lozouet P., Phuong M.A., Zaharias P. & Puillandre N. 2018. Exon-Capture-Based Phylogeny and Diversification of the Venomous Gastropods (Neogastropoda, Conoidea), in Vidal N. (Ed.), Molecular Biology and Evolution 35(10): 2355-2374. DOI:10.1093/molbev/msy144
???msg.biblio.abstract.label??? [+] [-]Transcriptome-based exon capture methods provide an approach to recover several hundred markers from genomic DNA, allowing for robust phylogenetic estimation at deep timescales. We applied this method to a highly diverse group of venomous marine snails, Conoidea, for which published phylogenetic trees remain mostly unresolved for the deeper nodes. We targeted 850 protein coding genes (678,322 bp) in ca. 120 samples, spanning all (except one) known families of Conoidea and a broad selection of non-Conoidea neogastropods. The capture was successful for most samples, although capture efficiency decreased when DNA libraries were of insufficient quality and/or quantity (dried samples or low starting DNA concentration) and when targeting the most divergent lineages. An average of 75.4% of proteins was recovered, and the resulting tree, reconstructed using both supermatrix (IQ-tree) and supertree (Astral-II, combined with the Weighted Statistical Binning method) approaches, are almost fully supported. A reconstructed fossil-calibrated tree dates the origin of Conoidea to the Lower Cretaceous. We provide descriptions for two new families. The phylogeny revealed in this study provides a robust framework to reinterpret changes in Conoidea anatomy through time. Finally, we used the phylogeny to test the impact of the venom gland and radular type on diversification rates. Our analyses revealed that repeated losses of the venom gland had no effect on diversification rates, while families with a breadth of radula types showed increases in diversification rates, thus suggesting that trophic ecology may have an impact on the evolution of Conoidea.
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CEAMARC-AA, CONCALIS, ???msg.security.private???, DongSha 2014, EXBODI, GUYANE 2014, ILES DU SALUT, INHACA 2011, KARUBENTHOS 2012, KAVIENG 2014, MAINBAZA, NORFOLK 2, NanHai 2014, PANGLAO 2005, PAPUA NIUGINI, ???msg.security.private???, SALOMONBOA 3, TAIWAN 2013, TERRASSES, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Ashrafi Hossein, Ďuriš Zdeněk & Anker Arthur 2024. Description and Phylogenetic Position of a New Genus and Species of Deep-Water Alpheid Shrimp Associated with Glass Sponges off New Caledonia (Decapoda: Caridea). Zoological Studies 無(63). DOI:10.6620/ZS.2024.63-03
???msg.biblio.abstract.label??? [+] [-]Batellopsis paula gen. et sp. nov., a new hexactinellid-associated alpheid shrimp, is described based on a single specimen collected at a depth of 477–503 m north of Île des Pins, New Caledonia. Batellopsis gen. nov. is part of a clade of four genera all containing hexactinellid-associated species, for which a molecular phylogeny is presented. The evolution of several morphological characters, including orbital teeth, a bulge- fossa system on the fingers of the first pereiopod chela, and groups of microserrulate setae on the second pereiopod chela, is discussed in light of phylogenetic results.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Bamber R.N. 2013. Deep-water Pycnogonida from recent cruises to Papua New Guinea and Melanesia, with an appendix of new records from Polynesia and descriptions of five new species. Zoosystema 35(2): 195-214. DOI:10.5252/z2013n2a5
???msg.biblio.abstract.label??? [+] [-]Deep-sea pycnogonid material collected during the N/O Alis Campagnes SalomonBOA 3 to the Solomon Islands in 2007, Terasses to New Caledonia in 2008, Tarasoc to the Tuamoto Archipelago and Tarava Seamounts in 2009, Biopapua to Papua New Guinea in 2010, and Exbodi to New Caledonia in 2011, has been analyzed. This includes the first collection of deep-sea pycnogonids from the waters of Papua New Guinea. The material includes 71 specimens from 14 species in seven genera. Most are frequently-recorded species of the genus Colossendeis, but there are also four species new to science, Ascorhynchus quartogibbus n. sp., Cilunculus roni n. sp., Phoxichilidium alis n. sp., Pycnogonum papua n. sp. A specimen from New Caledonia, identified by Stock in 1997 as Pycnogonum occa Loman, 1908, but not figured or described, has been re-examined, and found also to be a distinct species, Pycnogonum staplesi n. sp.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Bitner A. 2015. Checklist of recent brachiopod species collected during the Terrasses and Exbodi cruises in the New Caledonian region, SW Pacific. ZooKeys 537: 33-50. DOI:10.3897/zookeys.537.6567
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IB (Bryozoaires Brachiopodes) -
Cairns S.D. 2015. Stylasteridae (Cnidaria: Hydrozoa: Anthoathecata) of the New Caledonian Region - Tropica Deep-Sea Benthos 28. Mémoires du Muséum national d'Histoire naturelle 207, 363 pp. ISBN:978-2-85653-767-1
???msg.biblio.biblioSurvey.label??? (31) [+] [-]AZTEQUE, BATHUS 2, BATHUS 3, BATHUS 4, BIOCAL, BIOGEOCAL, CALSUB, CHALCAL 1, CHALCAL 2, CONCALIS, CORAIL 2, EBISCO, EXBODI, HALIPRO 1, LAGON, LITHIST, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, TERRASSES, VAUBAN 1978-1979, VOLSMAR
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Castelin M., Williams S.T., Buge B., Maestrati P., Lambourdière J., Ozawa T., Utge J., Couloux A., Alf A. & Samadi S. 2017. Untangling species identity in gastropods with polymorphic shells in the genus Bolma Risso, 1826 (Mollusca, Vetigastropoda). European Journal of Taxonomy 288: 1-21. DOI:10.5852/ejt.2017.288
???msg.biblio.abstract.label??? [+] [-]In shelled molluscs, assigning valid species names to independent evolutionary lineages can be a difficult task. Most original descriptions are based on empty shells and the high levels of variation in shape, color and pattern in some groups can make the shell a poor proxy for species-level identification. The deep-sea gastropod turbinid genus Bolma is one such example, where species-level identification based on shell characters alone is challenging. Here, we show that in Bolma both traditional and molecular taxonomic treatments are associated with a number of pitfalls that can lead to biased inferences about species diversity. Challenges derive from the few phylogenetically informative characters of shells, insufficient information provided in original descriptions and sampling artefacts, which at the molecular level in spatially fragmented organisms can blur distinctions between genetically divergent populations and separate species. Based on a comprehensive dataset combining molecular, morphological and distributional data, this study identified several cases of shell-morphological plasticity and convergence. Results also suggest that what was thought to be a set of distinct, range-restricted species corresponds instead to a smaller number of more widespread species. Overall, using an appropriate sampling design, including type localities, allowed us to assign available names to evolutionarily significant units.
???msg.biblio.biblioSurvey.label??? (16) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, BORDAU 1, CONCALIS, EBISCO, EXBODI, MAINBAZA, MIRIKY, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, SALOMON 2, SALOMONBOA 3, TAIWAN 2004, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Chan B.K., Chen H.N., Rodriguez Moreno P.A. & Corbari L. 2016. Diversity and biogeography of the little known deep-sea barnacles of the genus Waikalasma Buckeridge, 1983 (Balanomorpha: Chionelasmatoidea) in the Southwest Pacific, with description of a new species. Journal of Natural History 50(47-48): 2961-2984. DOI:10.1080/00222933.2016.1226445
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Chan B.K., Corbari L., Rodriguez Moreno P.A. & Tsang L.M. 2017. Molecular phylogeny of the lower acorn barnacle families (Bathylasmatidae, Chionelasmatidae, Pachylasmatidae and Waikalasmatidae)(Cirripedia: Balanomorpha) with evidence for revisions in family classification. Zoological Journal of the Linnean Society 180: 542-555
???msg.biblio.biblioSurvey.label??? (16) [+] [-]ATIMO VATAE, BIOPAPUA, BORDAU 1, BORDAU 2, EBISCO, EXBODI, MUSORSTOM 10, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, SALOMON 1, SALOMON 2, SANTO 2006, SMIB 3, SMIB 5, TARASOC
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Chan T., Ma K.Y. & Chu K.H. 2013. The deep-sea spiny lobster genus Puerulus Ortmann, 1897 (Crustacea, Decapoda, Palinuridae), with descriptions of five new species, in Ahyong S.T., Chan T., Corbari L. & Ng P.K.(Eds), Tropical Deep-Sea Benthos 27. Mémoires du Muséum national d'Histoire naturelle 204:191-230, ISBN:978-2-85653-692-6
???msg.biblio.abstract.label??? [+] [-]Recent French deep-sea expeditions in the Indo-West Pacific resulted in the collection of abundant material of the deep-sea lobster genus Puerulus Ortmann, 1897 (Palinuridae). Difficulties in identification necessitated a generic revision and as a result, five new species are described, all of which are similar to P. angulatus (Bate, 1888). Puerulus angulatus was thought to have a wide distribution from eastern Africa to Marquesas Islands, but is now restricted to the western Pacific, from Japan to Australia. Of the five new species, P. gibbosus n. sp. is found in eastern Africa, P. mesodontus n. sp. from Japan to Fiji, P. richeri n. sp. from the New Caledonia to Marquesas Islands, while P. sericus n. sp. and P. quadridentis n. sp. mainly occur around New Caledonia. Of the other three previously described species, the distribution of P. velutinus Holthuis, 1963, is extended to Fiji, while P. sewelli Ramadan, 1938, and P. carinatus Borradaile, 1910, are still only known from the northern and western parts of the Indian Ocean, respectively. COI gene sequence differences support the morphological species distinctions.
???msg.biblio.biblioSurvey.label??? (54) [+] [-]AURORA 2007, AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHEDI, BERYX 11, BERYX 2, BIOCAL, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, CHALCAL 1, CHALCAL 2, ???msg.security.private???, EBISCO, EXBODI, HALIPRO 1, KARUBAR, LITHIST, MAINBAZA, ???msg.security.private???, MIRIKY, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PALEO-SURPRISE, PANGLAO 2005, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMCB, SMIB 1, SMIB 2, SMIB 4, SMIB 8, TAIWAN 2001, TARASOC, TERRASSES, VAUBAN 1978-1979, VOLSMAR
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Chen H.P., Lee M.Y. & Chen W.J. 2024. Integrative taxonomy reveals unanticipated hidden diversity in the monotypic goosefish genus Lophiomus (Teleostei, Lophiidae), with description of three new species and resurrection of Chirolophius laticeps Ogilby, 1910. European Journal of Taxonomy 943: 239–287. DOI:10.5852/ejt.2024.943.2599
???msg.biblio.abstract.label??? [+] [-]Thought to be monotypic for decades, the only species in the goosefish genus Lophiomus Gill, Lm. setigerus (Vahl), shows a wide range of morphological variation and is distributed widely in the Indo-West Pacific (IWP). In this study, datasets for two mitochondrial and two nuclear genes sequences obtained from samples of Lophiomus collected in different localities across the IWP were constructed and analyzed to explore the phylogeny and species diversity within the genus. Our integrated approach with multiline evidence unveiled an unanticipated richness of at least six delimited species of Lophiomus. Herein, based on materials already available from museums and new specimens obtained primarily through the Tropical Deep-Sea Benthos program surveying IWP benthic fauna, we formally describe three new species: Lm. immaculioralis sp. nov., Lm. nigriventris sp. nov., and Lm. carusoi sp. nov. Also, we resurrect Lm. laticeps stat. rev. from synonyms of Lm. setigerus. These species can be diagnosed by genetics, body coloration, patterns on the floor of the mouth, peritoneum pigmentation, morphometric measurements, and meristic counts of cranial spines, dorsal-fin spines, and pectoral-fin and pelvic-fin rays from each other and from Lm. setigerus. The species Lm. setigerus, as well as the genus Lophiomus, are re-described accordingly based on the new results. Amended identification keys to the four extant lophiid genera and to species of Lophiomus are also provided.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Chen J.N., Samadi S. & Chen W.J. 2018. Rhodopsin gene evolution in early teleost fishes. PLOS ONE 13(11): e0206918. DOI:10.1371/journal.pone.0206918
???msg.biblio.abstract.label??? [+] [-]Rhodopsin mediates an essential step in image capture and is tightly associated with visual adaptations of aquatic organisms, especially species that live in dim light environments (e.g., the deep sea). The rh1 gene encoding rhodopsin was formerly considered a singlecopy gene in genomes of vertebrates, but increasing exceptional cases have been found in teleost fish species. The main objective of this study was to determine to what extent the visual adaptation of teleosts might have been shaped by the duplication and loss of rh1 genes. For that purpose, homologous rh1/rh1-like sequences in genomes of ray-finned fishes from a wide taxonomic range were explored using a PCR-based method, data mining of public genetic/genomic databases, and subsequent phylogenomic analyses of the retrieved sequences. We show that a second copy of the fish-specific intron-less rh1 is present in the genomes of most anguillids (Elopomorpha), Hiodon alosoides (Osteoglossomorpha), and several clupeocephalan lineages. The phylogenetic analysis and comparisons of alternative scenarios for putative events of gene duplication and loss suggested that fish rh1 was likely duplicated twice during the early evolutionary history of teleosts, with one event coinciding with the hypothesized fish-specific genome duplication and the other in the common ancestor of the Clupeocephala. After these gene duplication events, duplicated genes were maintained in several teleost lineages, whereas some were secondarily lost in specific lineages. Alternative evolutionary schemes of rh1 and comparison with previous studies of gene evolution are also reviewed.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Criscione F., Hallan A., Puillandre N. & Fedosov A. 2021. Snails in depth: integrative taxonomy of Famelica, Glaciotomella and Rimosodaphnella (Conoidea: Raphitomidae) from the deep sea of temperate Australia. Invertebrate Systematics 35(8): 940-962. DOI:10.1071/IS21008
???msg.biblio.abstract.label??? [+] [-]The deep sea of temperate south-eastern Australia appears to be a ‘hotspot’ for diversity and endemism of conoidean neogastropods of the family Raphitomidae. Following a series of expeditions in the region, a considerable amount of relevant DNA-suitable material has become available. A molecular phylogeny based on this material has facilitated the identification of diagnostic morphological characters, allowing the circumscription of monophyletic genera and the introduction of several new genus-level taxa. Both named and new genera are presently being investigated through integrative taxonomy, with the discovery of a significant number of undescribed species. As part of this ongoing investigation, our study focuses on the genera Famelica Bouchet & Warén, 1980, Glaciotomella Criscione, Hallan, Fedosov & Puillandre, 2020 and Rimosodaphnella Cossmann, 1914. We subjected a comprehensive mitochondrial DNA dataset of representative deep-sea raphitomids to the species delimitation methods ABGD and ASAP that recognised 18 and 15 primary species hypotheses (PSHs) respectively. Following additional evaluation of shell and radular features, and examination of geographic and bathymetric ranges, nine of these PSHs were converted to secondary species hypotheses (SSHs). Four SSHs (two in Famelica and two in Rimosodaphnella) were recognised as new, and formal descriptions are provided herein.
???msg.biblio.biblioSurvey.label??? (14) [+] [-]AURORA 2007, BIOPAPUA, BOA1, EXBODI, KANACONO, KAVIENG 2014, MAINBAZA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, TARASOC, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Cunha T.J., Lemer S., Bouchet P., Kano Y. & Giribet G. 2019. Putting keyhole limpets on the map: phylogeny and biogeography of the globally distributed marine family Fissurellidae (Vetigastropoda, Mollusca). Molecular Phylogenetics and Evolution 135: 249-269. DOI:10.1016/j.ympev.2019.02.008
???msg.biblio.abstract.label??? [+] [-]Fissurellidae are marine gastropods with a worldwide distribution and a rich fossil record. We integrate molecular, geographical and fossil data to reconstruct the fissurellid phylogeny, estimate divergence times and investigate historical routes of oceanic dispersal. With five molecular markers for 143 terminals representing 27 genera, we resolve deep nodes and find that many genera (e.g., Emarginula, Diodora, Fissurella) are not monophyletic and need systematic revision. Several genera classified as Emarginulinae are recovered in Zeidorinae. Future work should prioritize emarginuline genera to improve understanding of ancestral traits and the early evolution of fissurellids. Tree calibration with the fossilized birth-death model indicates that crown fissurellids originated around 175 Ma, and generally resulted in younger ages for the earliest nodes than the node dating approach. Model-based biogeographic reconstruction, supported by fossils, infers an Indo-West Pacific origin, with a westward colonization of new oceans via the Tethys Seaway upon the breakup of Pangea. Western Atlantic clades then served as source for dispersal towards other parts of the globe. As the sister group to all other fissurellids, Rimula is ranked in its own subfamily, Rimulinae stat. nov. New synonyms: Hemitominae syn. nov. of Zeidorinae stat. nov.; Cranopsis syn. nov. of Puncturella; Variegemarginula syn. nov. of Montfortula.
???msg.biblio.biblioSurvey.label??? (14) [+] [-]ATIMO VATAE, AURORA 2007, CEAMARC-AA, CONCALIS, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, TARASOC
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Cunha T.J., Lemer S., Bouchet P., Kano Y. & Giribet G. 2019. Putting keyhole limpets on the map: phylogeny and biogeography of the globally distributed marine family Fissurellidae (Vetigastropoda, Mollusca). Molecular Phylogenetics and Evolution 135: 249-269. DOI:10.1016/j.ympev.2019.02.008
???msg.biblio.abstract.label??? [+] [-]Fissurellidae are marine gastropods with a worldwide distribution and a rich fossil record. We integrate molecular, geographical and fossil data to reconstruct the fissurellid phylogeny, estimate divergence times and investigate historical routes of oceanic dispersal. With five molecular markers for 143 terminals representing 27 genera, we resolve deep nodes and find that many genera (e.g., Emarginula, Diodora, Fissurella) are not monophyletic and need systematic revision. Several genera classified as Emarginulinae are recovered in Zeidorinae. Future work should prioritize emarginuline genera to improve understanding of ancestral traits and the early evolution of fissurellids. Tree calibration with the fossilized birth-death model indicates that crown fissurellids originated around 175 Ma, and generally resulted in younger ages for the earliest nodes than the node dating approach. Model-based biogeographic reconstruction, supported by fossils, infers an Indo-West Pacific origin, with a westward colonization of new oceans via the Tethys Seaway upon the breakup of Pangea. Western Atlantic clades then served as source for dispersal towards other parts of the globe. As the sister group to all other fissurellids, Rimula is ranked in its own subfamily, Rimulinae stat. nov. New synonyms: Hemitominae syn. nov. of Zeidorinae stat. nov.; Cranopsis syn. nov. of Puncturella; Variegemarginula syn. nov. of Montfortula.
???msg.biblio.biblioSurvey.label??? (14) [+] [-]ATIMO VATAE, AURORA 2007, CEAMARC-AA, CONCALIS, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, TARASOC
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fassio G., Russo P., Bonomolo G., Fedosov A.E., Modica M., Nocella E. & Oliverio M. 2022. A molecular framework for the systematics of the Mediterranean spindle-shells (Gastropoda, Neogastropoda, Fasciolariidae, Fusininae). Mediterranean Marine Science 23(3): 623-636. DOI:10.12681/mms.29935
???msg.biblio.abstract.label??? [+] [-]A remarkably high diversity of native small spindle-shells (Gastropoda, Fasciolariidae, Fusininae) has been recently inventoried in the Mediterranean Sea, with 23 species identified based on shell morphology. They have almost invariably been classified in the genus Fusinus, and a few of them recently moved to other genera (Aptyxis Troschel 1868, Aegeofusinus Russo, 2017 and Gracilipurpura Jousseaume, 1880), mostly based on the sole shell features. We have reconstructed a molecular phylogenetic framework for the Mediterranean Fusininae, focusing on native species representative of the genus-level taxa. Our results confirmed that Fusinus s.s. (type species Murex colus Linnaeus, 1758) should be restricted to a group of large-shelled species from the Indo-West Pacific and does not fit any of the small-shelled Mediterranean fusinines. We confirm that Murex syracusanus Linnaeus, 1758 represents a distinct lineage, and show that for all the remaining species the pattern is suggestive of a single monophyletic radiation of small Mediterranean fusinines, for which the name Pseudofusus Monterosato, 1884 must be used
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, AURORA 2007, CONCALIS, ???msg.security.private???, EBISCO, EXBODI, GUYANE 2014, KANACONO, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MIRIKY, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, TARASOC, TERRASSES, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedesov A.E., Puillandre N., Herrmann M., Dgebuadze P. & Bouchet P. 2017. Phylogeny, systematics, and evolution of the family Costellariidae (Gastropoda: Neogastropoda). Zoological Journal of the Linnean Society 179(3): 541-626. DOI:https://doi.org/10.1111/zoj.12431
???msg.biblio.abstract.label??? [+] [-]The neogastropod family Costellariidae is a large and successful group of carnivorous marine mollusks that encompasses about 475 living species. Costellariids are most diverse in the tropical Indo-Pacific at a depth interval of 0–200 m, where they are largely represented by numerous species commonly assigned to the genus Vexillum. The present work expands the taxon sampling of a previous phylogeny of the mitriform gastropods to resolve earlier problematic relationships, and thus establish a robust framework of the family, revise its taxonomy, and uncover major trends in the evolution of costellariid morphology. A multicuspidate rachidian is shown to have appeared at least twice in the evolutionary history of the family: it is regarded as an apomorphy of the primarily Indo-Pacific Vexillum–Austromitra–Atlantilux lineage, and has evolved independently in the Nodicostellaria–Mitromica lineage of the western hemisphere. The genera Ceratoxancus and Latiromitra are transferred from the Ptychatractidae to the Costellariidae. Tosapusia, Protoelongata, and Pusia are ranked as full genera, the latter with the three subgenera Pusia, Ebenomitra, and Vexillena. Vexillum (Costellaria) and Zierliana are treated as synonyms of Vexillum. The replacement name Suluspira is proposed for Visaya Poppe, Guillot de Suduiraut & Tagaro, 2006, non Ahyong, 2004 (Crustacea). We introduce four new genera, Alisimitra, Costapex, Turriplicifer, and Orphanopusia, and characterize their anatomy; 14 new species, mostly from deep water in the Indo-Pacific, are described in the genera Tosapusia, Alisimitra, Costapex, and Pusia. At least two species of Costapex gen. nov. have been collected from sunken wood.
???msg.biblio.biblioSurvey.label??? (29) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 3, BENTHAUS, BIOCAL, BIOPAPUA, BOA1, CONCALIS, EBISCO, EXBODI, KARUBENTHOS 2012, KAVIENG 2014, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 2, SMIB 4, TARASOC, TERRASSES, Tuhaa Pae 2013, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Fedosov A., Puillandre N., Kantor Y. & Bouchet P. 2015. Phylogeny and systematics of mitriform gastropods (Mollusca: Gastropoda: Neogastropoda): Phylogeny of Mitriform Gastropods. Zoological Journal of the Linnean Society 175(2): 336-359. DOI:10.1111/zoj.12278
???msg.biblio.abstract.label??? [+] [-]With about 800 Recent species, ‘miters’ are a widely distributed group of tropical and subtropical gastropods that are most diverse in the Indo-West Pacific. They include the two families Mitridae and Costellariidae, similar in shell morphology and traditionally treated as close relatives. Some genera of deep-water Ptychatractidae and Volutomitridae are close to miters in shell morphology, and the term ‘mitriform gastropods’ has been introduced to refer to Mitridae, Costellariidae, and this assortment of convergent forms. The present study aimed at the reconstruction of phylogenetic relationships of mitriform gastropods based on representative taxon sampling. Four genetic markers [cytochrome c oxidase subunit I (COI), 16S and 12S rRNA mitochondrial genes, and H3 (Histone 3) nuclear gene] were sequenced for over 90 species in 20 genera, and the molecular data set was supplemented by studies of radula morphology. Our analysis recovered Mitridae as a monophyletic group, whereas the genus Mitra was found to be polyphyletic. Of 42 mitrid species included in the analysis, 37 formed a well-supported ‘core Mitridae’ consisting of four major clades, three of them consistent with the subfamilies Cylindromitrinae, Imbricariinae, and Mitrinae, and Strigatella paupercula standing out by itself. Basal to the ‘core Mitridae’ are four minor lineages, with the genus Charitodoron recognized as sister group to all other Mitridae. The deepwater family Pyramimitridae shows a sister relationship to the Mitridae, with high support for a Pyramimitridae + Mitridae clade. Our results recover the monophyly of the Costellariidae, which form a wellsupported clade that also includes Ptychatractidae, Columbariinae, and Volutomitridae, but not Mitridae. Most derived and diverse amongst Costellariidae are species of Vexillum, characterized by a bow-shaped, multicuspidate rachidian tooth. Several previously unrecognized deep-water costellariid lineages are revealed. Their members retain some plesiomorphies – in particular a tricuspidate rachidian tooth – that makes them morphologically intermediate between ptychatractids and Vexillum. The taxa of Ptychatractidae included in the analysis are not monophyletic, but form three well-supported, unrelated groupings, corresponding respectively to Ceratoxancus + Latiromitra, Exilia, and Exiliodea. None of them shows an affinity to Pseudolividae.
???msg.biblio.biblioSurvey.label??? (21) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, INHACA 2011, MAINBAZA, MIRIKY, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, ???msg.security.private???, SALOMON 2, SALOMONBOA 3, SANTO 2006, TARASOC, TERRASSES, Tuhaa Pae 2013, ???msg.security.private???
???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. 2015. Centrodraco fidelis (Draconettidae), a new deepwater dragonet species from the southern Loyalty Ridge, southwestern Pacific Ocean. Cybium 39(3): 211-217
???msg.biblio.abstract.label??? [+] [-]Centrodraco fidelis sp. nov. is described from three specimens, which were collected on the southern Loyalty Ridge (New Caledonian EEZ) during the oceanographic cruise EXBODI. The species is characterised by: 14 rays in the second dorsal fin; 13 rays in the anal fin; first dorsal fin with the second spine elongate and filamentous in the male; second dorsal fin very low, without filaments in the male; opercular spine 1.8-2.4 in subopercular spine; body slightly compressed; body depth 7.4-8.5% of SL; body width 7.7-8.8% of SL; pectoral fin short, not reaching to anus when adpressed; pectoral fin length 9.9-11.8% of SL; male body colour pattern pale, with a single grey spot on the beginning of the lower lateral line; filament in first dorsal fin pale, fin with a large basal dark blotch; the male anal fin with three dark blotches. The new species is compared with allied species. A revised key to the genera and species of Draconettidae presented.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Fricke R., Teitelbaum A. & Wantiez L. 2015. Twenty-one new records of fish species (Teleostei) from the New Caledonian EEZ (south-western Pacific Ocean). Marine Biodiversity Records 8: e123. DOI:10.1017/S1755267215000986
???msg.biblio.abstract.label??? [+] [-]New records of fish species are reported from New Caledonia, including Polyipnus aquavitus Baird, 1971 (Sternoptychidae), Porogadus melampeplus (Alcock, 1896) (Ophidiidae), Hoplichthys citrinus Gilbert 1905 (Hoplichthyidae), Plectrogenium nanum Gilbert 1905 (Plectrogeniidae), Lioscorpius trifasciatus Last, Yearsley & Motomura 2005 (Setarchidae), Neomerinthe megalepis Fowler 1938 and Phenacoscorpius megalops Fowler 1938 (Scorpaenidae), Ocosia apia Poss & Eschmeyer, 1975 (Tetrarogidae), Hoplostethus atlanticus Collett 1889 (Trachichthyidae), Zenion longipinnis Kotthaus, 1970 (Zeniontidae), Plectranthias foresti Fourmanoir 1977, Plectranthias pelicieri Randall & Shimizu, 1994, Plectranthias rubrifasciatus Fourmanoir & Randall, 1979 and Rabaulichthys squirei Randall & Walsh, 2010 (Serranidae), Synagrops philippinensis (Gu¨nther 1880) (Acropomatidae), Stegastes insularis Allen & Emery 1995 (Pomacentridae), Cirrhilabrus rubrimarginatus Randall 1992 (Labridae), Pteropsaron neocaledonicus Fourmanoir & Rivaton, 1979 (Percophidae), Centrodraco ornatus (Fourmanoir & Rivaton, 1979) and Draconetta xenica Jordan & Fowler 1903 (Draconettidae), and Acanthurus maculiceps (Ahl 1923) (Acanthuridae). A record of Plectropomus maculatus (Bloch 1790) (Serranidae) from Grande Terre, New Caledonia is confirmed. This paper also includes new depth records of Zenion longipinnis, Plectranthias rubrifasciatus, Synagrops philippinensis, Centrodraco ornatus and Draconetta xenica.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Fricke R. 2022. Obliquogobius bathyalis, a new species of deep-living gobies (Teleostei: Gobiidae) from New Caledonia, southwestern Pacific Ocean. FishTaxa 24: 1-9
???msg.biblio.abstract.label??? [+] [-]A new species of deep-water goby, Obliquogobius bathyalis n. sp. from New Caledonia, is described on the basis of three specimens collected with trawls at 264-350 m depth. The new species is characterised by the following characters: second dorsal-fin rays I, 8; anal-fin rays I,8 or I,9; head length 29.4-36.7% of SL; eye diameter 41.5-52.35 of head length; longitudinal scale rows 24-26; transverse scale rows 9-10; no predorsal scales; no scales on lateral surface of nape; postorbital pore G absent (from anterior oculoscapular canal); gill opening wide; caudal fin asymmetrical dorsoventrally, rays of upper half much longer than those of lower half, giving obliquely pointed appearance; four or five vertical dark bars on lower side of body; first dorsal fin distally with large black blotch; caudal fin distally dark; distinct dark spot on centre of caudal-fin base present. The new species is compared with other species in the genus. A revised key to the species of Obliquogobius is presented.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Galil B.S. 2013. The deep water box crab Calappa karenae (Crustacea: Decapoda: Brachyura): a new record from Melanesia. Marine Biodiversity Records 6(e76): 1-2. DOI:http://dx.doi.org/10.1017/S175526721300050X
???msg.biblio.abstract.label??? [+] [-]Calappa karenae, is here documented from Loyalty Islands, Melanesia, based on a specimen collected in September 2011. This rare deep water box crab was previously known only from a pair of specimens collected in off Guam, Micronesia, a distance of 4000 km away.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Galindo L.A., Puillandre N., Utge J., Lozouet P. & Bouchet P. 2016. The phylogeny and systematics of the Nassariidae revisited (Gastropoda, Buccinoidea). Molecular Phylogenetics and Evolution 99: 337-353. DOI:10.1016/j.ympev.2016.03.019
???msg.biblio.abstract.label??? [+] [-]Nassariidae are a group of scavenging, predominantly marine, snails that are diversified on soft bottoms as well as on rocky shores, and are the subject of numerous research papers in ecology, ecotoxicology or paleontology. A weak and/or apparently continuous variation in shell characters has resulted in an intimidating taxonomy, with complex synonymy lists. Over 1320 extant nominal species have been described, of which 442 are currently regarded as valid. Above species level, the state of the art is equally hazy, with four subfamilies and twelve genera currently accepted, and many other names in the graveyard of synonymy. A molecular analysis based on three mitochondrial (COI, 16S, 12S) and two nuclear (28S, H3) markers was conducted. Our dataset includes 218 putative nassariid species, comprising 9 of the 12 valid genera, and 25 nominal genera represented by their type species. The monophyly of the Nassariidae as classically construed is not confirmed. Species of Antillophos, Engoniophos, Phos, Nassaria, Tomlinia and Anentome (formerly considered Buccinidae) are included inside the Nassariidae clade. Within the Nassariinae, the tree unexpectedly demonstrates that species from the Atlantic and the Indo-Pacific form different clades which represent several independent diversification events. Through an integrative approach, the reconstruction of ancestral states was addressed for eight characters supposedly informative for taxonomy. Using numerous fossil calibration points, Nassariidae appear to have originated 120 MYA ago in Atlantic temperate waters during the Lower Cretaceous. Our results have a profound impact on nassariid taxonomy, especially with regard to the validity of subfamily- and genus-level names.
???msg.biblio.biblioSurvey.label??? (19) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, INHACA 2011, KARUBENTHOS 2012, LIFOU 2000, MAINBAZA, MIRIKY, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, SALOMON 2, SALOMONBOA 3, SANTO 2006, TARASOC, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Hallan A., Criscione F., Fedosov A. & Puillandre N. 2021. Few and far apart: integrative taxonomy of Australian species of Gladiobela and Pagodibela (Conoidea : Raphitomidae) reveals patterns of wide distributions and low abundance. Invertebrate Systematics 35: 181-202. DOI:10.1071/IS20017
???msg.biblio.abstract.label??? [+] [-]The deep-sea malacofauna of temperate Australia remains comparatively poorly known. However, a recent influx of DNA-suitable material obtained from a series of deep-sea cruises has facilitated integrative taxonomic study on the Conoidea (Caenogastropoda : Neogastropoda). Building on a recent molecular phylogeny of the conoidean family Raphitomidae, this study focussed on the genera Gladiobela and Pagodibela (both Criscione, Hallan, Puillandre & Fedosov, 2020). We subjected a representative mtDNA cox1 dataset of deep-sea raphitomids to ABGD, which recognised 14 primary species hypotheses (PSHs), 9 of which were converted to secondary species hypotheses (SSHs). Following the additional examination of the shell and hypodermic radula features, as well as consideration of bathymetric and geographic data, seven of these SSHs were recognised as new to science and given full species rank. Subsequently, systematic descriptions are provided herein. Of these, five are attributed to Gladiobela (three of which are endemic to Australia and two more widely distributed) and two are placed in Pagodibela (one endemic to southern Australia and one widespread in the Pacific). The rarity of many ‘turrids’ reported in previous studies is confirmed herein, as particularly indicated by highly disjunct geographic records for two taxa. Additionally, several of the studied taxa exhibit wide Indo-Pacific distributions, suggesting that wide geographic ranges in deep-sea ‘turrids’ may be more common than previously assumed. Finally, impediments to deep-sea ‘turrid’ taxonomy in light of such comparative rarity and unexpectedly wide distributions are discussed.
???msg.biblio.biblioSurvey.label??? (11) [+] [-]ATIMO VATAE, BIOMAGLO, BIOPAPUA, BOA1, EBISCO, EXBODI, KANACONO, PAPUA NIUGINI, SALOMON 2, TARASOC, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Herbert D.G. 2024. The Umboniinae (Mollusca: Gastropoda: Trochidae) of New Caledonia, with descriptions of two new genera and eight new species, plus an additional new species from the Bismarck Sea. European Journal of Taxonomy 973: 1-143. DOI:10.5852/ejt.2024.973.2765
???msg.biblio.abstract.label??? [+] [-]All species of Umboniinae known to occur in New Caledonia are discussed (19 species, 8 new, belonging to 10 genera, 2 new) and a key to genera is provided. An additional new species is described from the Bismarck Sea. Nine species are perhaps endemic to New Caledonia. The diversity of the fauna is comparable to that of Japan and Australia, both regions of much greater extent and spanning a much broader latitudinal range. Ethalia lampra (Watson, 1880), previously known only from the original HMS Challenger material from Fiji, has been rediscovered in New Caledonia. Re-examination of the type material of Monilea apicina Gould, 1861 has led to a re-interpretation of the application of this name. Type specimens of a number of additional umboniine species examined for comparison are illustrated. Two new genera are proposed: Kanakina gen. nov. and Tylorhaphe gen. nov. Nine new species are described: Ethalia anomphala sp. nov., Ethminolia hickmanae sp. nov., Sericominolia porcata sp. nov., S. safrocincta sp. nov., Talopena maestratii sp. nov., Tylorhaphe alisae gen. et sp. nov., T. fritillaria gen. et sp. nov., T. luteopicta gen. et sp. nov. and T. wallacei gen. et sp. nov. Revised status: Talopena Iredale, 1918 is recognised as a full genus rather than a subgenus or synonym of Monilea Swainson, 1840. Minolia agapeta Melvill & Standen, 1896 is considered a distinct species, no longer to be regarded as a junior synonym of Monilea apicina Gould, 1861. Trochus (Monilea) lifuanus Fischer, 1878 is considered a distinct species, no longer to be regarded as a junior synonym of Monilea vernicosa Gould, 1861. New combinations: Monilea incerta Iredale, 1912 is reassigned to Talopena Iredale, 1918; Monilea apicina Gould, 1861, Monilea menkei A. Adams, 1855, Monilea philippii A. Adams, 1855, Pseudominolia tramieri Poppe, Tagaro & Dekker, 2006, Trochus belcheri Philippi, 1850, Trochus calyculus W. Wood, 1828, and Trochus (Monilea) masoni G. Nevill & H. Nevill, 1874 are all referred to Talopena Iredale, 1918. Minolia glaphyrella Melvill & Standen, 1895 is transferred to Kanakina gen. nov. Type localities: Nouméa, New Caledonia is designated as the type locality for Trochus nucleus Philippi 1850; the type locality ‘Port Jackson’ originally given for Monilea apicina Gould, 1861 is considered erroneous and is emended to Lansdowne Bank. New records for New Caledonian marine ecoregion: Ethalia lampra (Watson, 1880), Talopena apicina (Gould, 1861) and ‘Talopena’ tramieri (Poppe, Tagaro & Dekker, 2006).
???msg.biblio.biblioSurvey.label??? (14) [+] [-]CHALCAL 1, CORAIL 2, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, LAGON, LIFOU 2000, MONTROUZIER, MUSORSTOM 6, SALOMON 1, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Ho H.C. & Chen W.J. 2013. DNA sequences and morphological variation in Lophiodes iwamotoi Ho, Séret & Shao, 2011 based on new material from New Caledonia. Zootaxa 3682(4): 594-598. DOI:10.11646/zootaxa.3682.4.12
???msg.biblio.abstract.label??? [+] [-]Iwamoto’s anglerfish Lophiodes iwamotoi is recorded from New Caledonia for the first time. Study of molecular features further support the validity of the species. Moloecular sequence data from the cytochrome c oxidase subunit-I and Rhodopsin loci, along with morphological variation are provided, as well as information on its fresh coloration.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Houart R. 2015. Four new species of Muricidae (Gastropoda) from New Caledonia, Papua New Guinea and Indonesia. The Nautilus 129(4): 143-155
???msg.biblio.abstract.label??? [+] [-]Four new species of Muricidae are described from New Caledonia, Papua New Guinea and Indonesia and compared with related species. One Timbellus species was collected in New Caledonia. Two other species are described from Papua New Guinea, respectively in Chicopinnatus and Dermomurex. The fourth species, also belonging in Chicopinnatus, originates from Indonesia.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Houart R., Zuccon D. & Puillandre N. 2019. Description of new genera and new species of Ergalataxinae (Gastropoda: Muricidae). Novapex 20(HS 12): 1-52
???msg.biblio.abstract.label??? [+] [-]The recent genetic analysis of the muricid subfamily Ergalataxinae has led to a better understanding of this subfamily, but some species were left without appropriate generic assignments and the classification of others required revision. This knowledge gap is partially filled herein, with new combinations and the description of three new genera. The examination of new material, along with a careful re-examination of and comparison to existing material, resulted also in the identification of nine new species. These new genera and new species are described herein, lectotypes are designated and new combinations are given. The geographical range of all the new species is provided on maps. All new species are compared with related or similar species. The radula of Morula palmeri Powell, 1967 is illustrated for the first time.
???msg.biblio.biblioSurvey.label??? (37) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 2, BENTHEDI, BERYX 11, BIOCAL, BIOMAGLO, BORDAU 2, CHALCAL 2, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBENTHOS 2, LIFOU 2000, MAINBAZA, MD32 (REUNION), ???msg.security.private???, MIRIKY, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SANTO 2006, SMCB, SMIB 3, SMIB 4, SMIB 5, SMIB 8, TERRASSES, Walters Shoal
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Houart R., Heros V. & Zuccon D. 2019. Description of Two New Species of Dermomurex (Gastropoda: Muricidae) with a Review of Dermomurex (Takia) in the Indo-West Pacifc. VENUS 78(1-2): 1-25. DOI:10.18941/venus.78.1-2_1
???msg.biblio.abstract.label??? [+] [-]The subgenus Dermomurex (Takia) is reviewed and one new species, D. (T.) manonae n. sp., is described from New Caledonia. It is distinguished from the similar D. (T.) wareni Houart, 1990 based on genetic differences and a few shell characters. From other species it differs in its shell and intritacalx morphology. The four Indo-West Pacific species are reviewed and illustrated, namely D. (T.) bobyini Kosuge, 1984, D. (T.) infrons Vokes, 1974, D. (T.) wareni Houart, 1990 and D. (T.) manonae n. sp. Dermomurex (subgenus?) paulinae n. sp. is described from New Caledonia in an undetermined subgenus and is distinguished from D. (D.) africanus Vokes, 1978 from South Africa by its shell and intritacalx morphology. Trialatella is synonymized with Dermomurex s.s.
???msg.biblio.biblioSurvey.label??? (32) [+] [-]ATIMO VATAE, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BIOCAL, CHALCAL 2, CONCALIS, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBAR, MIRIKY, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, TAIWAN 2000, TAIWAN 2002, TAIWAN 2004, TERRASSES, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Houart R., Buge B. & Zuccon D. 2021. A TAXONOMIC UPDATE OF THE TYPHINAE (GASTROPODA: MURICIDAE) WITH A REVIEW OF NEW CALEDONIA SPECIES AND THE DESCRIPTION OF NEW SPECIES FROM NEW CALEDONIA, THE SOUTH CHINA SEA AND WESTERN AUSTRALIA. Journal of Conchology 44(2): 103-147
???msg.biblio.abstract.label??? [+] [-]The classification of the subfamily Typhinae is revised based on a molecular phylogenetic analysis. The genera Typhina Jousseaume, 1880, Typhisopsis Jousseaume, 1880 and Typhisala Jousseaume, 1881 are here treated as synonyms, and Typhina is given precedence over Typhisopsis. Trubatsa Dall, 1889 is confirmed as a separate, valid genus, based on morphological shell characters and molecular analysis. Choreotyphis Iredale, 1936 is also regarded as a valid genus but still requires validation by molecular analysis. An appendix of Recent Typhinae includes a short description of each genus. The list of Typhinae recorded from New Caledonia is updated. The validity of Trubatsa lozoueti (Houart, 1991), a species so far known only from the empty collected holotype, is confirmed by the morphological and molecular analysis of a second specimen.
???msg.biblio.biblioSurvey.label??? (26) [+] [-]BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, BIOGEOCAL, CHALCAL 2, CONCALIS, EXBODI, HALIPRO 1, KANACONO, KANADEEP, KOUMAC 2.3, LAGON, LITHIST, MONTROUZIER, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, PALEO-SURPRISE, SMIB 3, TERRASSES, VAUBAN 1978-1979
???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., Roberts N.W., Strong E.E., Kano Y., Speiser D.I., Harper E.M. & Williams S.T. 2024. Evolution of Large Eyes in Stromboidea (Gastropoda): Impact of Photic Environment and Life History Traits, in Esposito L. (Ed.), Systematic Biology: syae063. DOI:10.1093/sysbio/syae063
???msg.biblio.abstract.label??? [+] [-]Abstract Eyes within the marine gastropod superfamily Stromboidea range widely in size, from 0.2 to 2.3 mm—the largest eyes known in any gastropod. Despite this interesting variation, the underlying evolutionary pressures remain unknown. Here, we use the wealth of material available in museum collections to explore the evolution of stromboid eye size and structure. Our results suggest that depth is a key light-limiting factor in stromboid eye evolution; here, increasing water depth is correlated with increasing aperture width relative to lens diameter, and therefore an increasing investment in sensitivity in dim light environments. In the major clade containing all large-eyed stromboid families, species observed active during the day and the night had wider eye apertures relative to lens sizes than species observed active during the day only, thereby prioritizing sensitivity over resolution. Species with no consistent diel activity pattern also had smaller body sizes than exclusively day-active species, which may suggest that smaller animals are more vulnerable to shell-crushing predators, and avoid the higher predation pressure experienced by animals active during the day. Within the same major clade, ancestral state reconstruction suggests that absolute eye size increased above 1 mm twice. The unresolved position of Varicospira, however, weakens this hypothesis and further work with additional markers is needed to confirm this result.
???msg.biblio.biblioSurvey.label??? (9) [+] [-]ATIMO VATAE, CONCALIS, EXBODI, INHACA 2011, KAVIENG 2014, KOUMAC 2.3, MADIBENTHOS, MIRIKY, PAPUA NIUGINI
???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) -
Jangoux M. 2022. The type specimens of extant asteroids (Echinodermata) in the Muséum national d'Histoire naturelle of Paris. Zoosystema 44(11). DOI:10.5252/zoosystema2022v44a11
???msg.biblio.abstract.label??? [+] [-]Since its foundation in 1793, type specimens of 441 asteroid species and subspecies have been deposited in the M uséum national d’Histoire naturelle of Paris. The annotated catalogue of all these taxa is drawn up including species whose type material could not be found in the collection. Today the Paris museum houses 1011 asteroid type specimens representing 398 nominal species and subspecies, most of which were described by Lamarck (1816), Müller & Troschel (1842), Perrier (between 1869 and 1896) and Koehler (between 1895 and 1923). Though originating worldwide, species coming from the Atlantic and Indo-West Pacific Oceans, and Antarctic waters are more numerous. A biographical directory of all those involved either in the descriptions of the species or the collection of new material as well as their dedicatee is annexed to the catalogue. Revision of the Paris collection allows to propose taxonomic changes for two species of Müller & Troschel (Echinaster crassus Müller & Troschel, 1842 and Echinaster gracilis Müller & Troschel, 1842 are synonymized with Echinaster purpureus (Gray, 1840)) and five species of Perrier (Asterias borbonica Perrier, 1875 and Echinaster clouei Perrier, 1869 are synonymized with Echinaster purpureus (Gray, 1840), Oreaster clouei Perrier, 1869 and Oreaster mammosus Perrier, 1869 with Protoreaster lincki (Blainville, 1830) and Ophidiaster chinensis Perrier, 1875 with Ophidiaster granifer Lütken, 1871).
???msg.biblio.biblioSurvey.label??? (27) [+] [-]BATHUS 1, BATHUS 3, BIOCAL, BIOMAGLO, CEAMARC-AA, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, EXBODI, HALIPRO 1, LITHIST, MIRIKY, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 2, SALOMON 2, SANTO 2006, SMIB 4, SMIB 5, SMIB 8, VAUBAN 1978-1979, Walters Shoal
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
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., Lozouet P., Puillandre N. & Bouchet P. 2014. Lost and found: The Eocene family Pyramimitridae (Neogastropoda) discovered in the Recent fauna of the Indo-Pacific. Zootaxa 3754(3): 239-276. DOI:10.11646/zootaxa.3754.3.2
???msg.biblio.abstract.label??? [+] [-]Most neogastropod families have a continuous record from the Cretaceous or Paleogene to the Recent. However, the fossil record also contains a number of obscure nominal families with unusual shell characters that are not adequately placed in the current classification. Some of these are traditionally regarded as valid, and some have been “lost” in synonymy. One such “lost” family is the Pyramimitridae, established by Cossmann in 1901 for the Eocene genus Pyramimitra, and currently included in the synonymy of Buccinidae. Examination of several species of inconspicuous, small turriform gastropods has revealed a radula type so far unknown in Neogastropoda, and their shell characters identify them as members of the "extinct" family Pyramimitridae. Neither the radular morphology nor the anatomy reveal the relationships of this enigmatic, “living fossil” family. Molecular data (12S, 16S, 28S, COI) confirm the recognition of Pyramimitridae as a distinct family, but no sister group was identified in the analysis. The family Pyramimitridae Cossmann, 1901, is thus restored as a valid family of Neogastropoda that includes the genera Pyramimitra Conrad, 1865, Endiatoma Cossmann, 1896, Vaughanites Woodring, 1928, Hortia Lozouet, 1999, and Teremitra new genus. Pyramimitrids occur in the Recent fauna at bathyal depths of the Indo- Pacific from Taiwan to Madagascar and New Zealand, with three genera and nine species (all but one new).
???msg.biblio.biblioSurvey.label??? (12) [+] [-]ATIMO VATAE, BIOCAL, BIOGEOCAL, BIOPAPUA, EXBODI, MUSORSTOM 8, NORFOLK 2, PANGLAO 2005, SALOMON 1, SANTO 2006, TAIWAN 2004, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Kantor Y.I., Fedosov A.E., Puillandre N. & Bouchet P. 2016. Integrative taxonomy approach to Indo-Pacific Olividae: new species revealed by molecular and morphological data. Ruthenica 26(2): 123-143
???msg.biblio.abstract.label??? [+] [-]Five new species of Olivoidea are described based on molecular and morphological evidence: four shallow subtidal Ancilla from Madagascar and Papua New Guinea, and one deep water (500-600 m) Calyptoliva from the Tuamotus. The sympatric – but not syntopic - Ancilla morrisoni and A. kaviengensis, from New Ireland province, are morphologically cryptic, differing mostly in shell colour, but are molecularly distinct. The sympatric – and possibly syntopic – Ancilla atimovatae and A. lhaumeti, belong to a species flock from southernmost Madagascar; A. atimovatae is conchologically nearly indistinguishable from A. ventricosa, but differs markedly in radular morphology. Calyptoliva was previously known only from the Coral Sea; C. bbugae is the first representative of the genus to yield molecular data. The new Ancilla are described based on sequenced holotypes; the type material of the new Calyptoliva includes a sequenced paratype.
???msg.biblio.biblioSurvey.label??? (9) [+] [-]
???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) -
Kitahara M.V. & Cairns S.D. 2021. Azooxanthellate Scleractinia (Cnidaria, Anthozoa) from New Caledonia 32. Mémoires du Muséum national d'histoire naturelle 215. Publications scientifiques du Muséum national d'histoire naturelle, Paris, 722 pp. ISBN:978-2-85653-935-4
???msg.biblio.biblioSurvey.label??? (49) [+] [-]AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BERYX 11, BIOCAL, BIOGEOCAL, BOA0, CHALCAL 1, CHALCAL 2, CONCALIS, CORAIL 2, EBISCO, EXBODI, GEMINI, HALICAL 1, HALIPRO 1, HALIPRO 2, KANACONO, KANADEEP 2, LAGON, LIFOU 2000, LITHIST, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PALEO-SURPRISE, SMIB 1, SMIB 10, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, TERRASSES, VAUBAN 1978-1979, VOLSMAR
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Kool H.H. & Galindo L.A. 2014. Description and Molecular Characterization of Six New Species of Nassarius (Gastropoda, Nassariidae) from the Western Pacific Ocean. American Malacological Bulletin 32(2): 147-164. DOI:10.4003/006.032.0202
???msg.biblio.abstract.label??? [+] [-]Six new species of the genus Nassarius Duméril, 1805 are described, based on material collected from the Coral Triangle and the South Pacific. We combine traditional morphology-based descriptions with the molecular (Cytochrome c oxidase I - COI) signature of the new species. New species are: Nassarius ocellatus sp. Nov. (Philippines to Vanuatu), Nassarius houbricki sp. Nov. (Solomon Islands to Queensland and Tonga), Nassarius radians sp. Nov. (Philippines to Vanuatu), Nassarius vanuatuensis sp. Nov. (Vanuatu), Nassarius velvetosus sp. Nov. (Western Australia to Fiji) and Nassarius martinezi sp. Nov. (Solomon Islands to Tonga).
???msg.biblio.biblioSurvey.label??? (29) [+] [-]AURORA 2007, BATHUS 1, BATHUS 2, BOA1, BORDAU 1, BORDAU 2, CHALCAL 1, CONCALIS, CORAIL 2, EBISCO, EXBODI, KARUBAR, LAGON, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, NORFOLK 2, PALEO-SURPRISE, PANGLAO 2004, PANGLAO 2005, SALOMON 1, SALOMONBOA 3, SANTO 2006, SMIB 6, ???msg.security.private???, TERRASSES, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Lee H., Chen W.J., Puillandre N., Aznar-Cormano L., Tsai M.H. & Samadi S. 2019. Incorporation of deep-sea and small-sized species provides new insights into gastropods phylogeny. Molecular Phylogenetics and Evolution 135: 136-147. DOI:10.1016/j.ympev.2019.03.003
???msg.biblio.abstract.label??? [+] [-]The use of phylogeny with uneven or limited taxon sampling may bias our interpretation of organismal evolution, for instance, the origin(s) of the deep-sea animals. The Mollusca is the second most speciose phylum, in which the Gastropoda forms the largest group. However, the currently proposed hypotheses of gastropod phylogeny are mainly based on part of their taxonomic diversity, notably on the large-sized and shallow-water species. In this study, we aimed at correcting this bias by reconstructing the phylogeny with new mitogenomes of deep-sea gastropods including Anatoma sp., Bathysciadiidae sp., Bayerotrochus teramachii, Calliotropis micraulax, Coccocrater sp., Cocculina subcompressa, Lepetodrilus guaymasensis, Peltospira smaragdina, Perotrochus caledonicus, Pseudococculinidae sp., and Shinkailepas briandi. This dataset provided the first reports of the mitogenomes for the Cocculiniformia, three vetigastropod superfamilies: Pleurotomarioidea, Lepetelloidea, and Scissurelloidea, and the neritimorph family Phenacolepadidae. The addition of deep-sea representatives also allowed us to evaluate the evolution of habitat use in gastropods. Our results showed a strongly supported sister-group relationship between the deep-sea lineages Cocculiniformia and Neomphalina. Within the Vetigastropoda, the Pleurotomarioidea was revealed as the sister-group of the remaining vetigastropods. Although this clade was presently restricted to the deep sea, fossil records showed that it has only recently invaded this habitat, thus suggesting that shallow waters was the ancestral habitat for the Vetigastropoda. The deep-sea Lepetelloidea and Lepetodriloidea formed a well-supported clade, with the Scissurelloidea sister to it, suggesting an early transition from shallow water to deep sea in this lineage. In addition, the switch between different chemosynthetic habitats was also observed in deep-sea gastropod lineages, notably in Neomphalina and Lepetelloidea. In both cases, the biogenic substrates appeared as the putative ancestral habitat, confirming the previously proposed hypothesis of a wooden-step to deep-sea vents scenario of evolution of habitat use for these taxa.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Lemer S., Buge B., Bemis A. & Giribet G. 2014. First molecular phylogeny of the circumtropical bivalve family Pinnidae (Mollusca, Bivalvia): Evidence for high levels of cryptic species diversity. Molecular Phylogenetics and Evolution 75: 11-23. DOI:10.1016/j.ympev.2014.02.008
???msg.biblio.abstract.label??? [+] [-]The family Pinnidae Leach, 1819, includes approximately 50 species of large subtidal and coastal marine bivalves. These commercially important species occur in tropical and temperate waters around the world and are most frequently found in seagrass meadows. The taxonomy of the family has been revised a number of times since the early 20th Century, the most recent revision recognizing 55 species distributed in three genera: Pinna, Atrina and Streptopinna, the latter being monotypic. However, to date no phylogenetic analysis of the family has been conducted using morphological or molecular data. The present study analyzed 306 pinnid specimens from around the world, comprising the three described genera and ca. 25 morphospecies. We sequenced the mitochondrial genes 16S rRNA and cytochrome c oxidase subunit I, and the nuclear ribosomal genes 18S rRNA and 28S rRNA. Phylogenetic analysis of the data revealed monophyly of the genus Atrina but also that the genus Streptopinna is nested within Pinna. Based on the strong support for this relationship we propose a new status for Streptopinna Martens, 1880 and treat it as a subgenus (status nov.) of Pinna Linnaeus, 1758. The phylogeny and the species delimitation analyses suggest the presence of cryptic species in many morphospecies displaying a wide Indo-Pacific distribution, including Pinna muricata, Atrina assimilis, A. exusta and P. (Streptopinna) saccata but also in the Atlantic species A. rigida. Altogether our results highlight the challenges associated with morphological identifications in Pinnidae due to the presence of both phenotypic plasticity and morphological stasis and reveal that many pinnid species are not as widely distributed as previously thought.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Lopes E.P., Santos S., Xavier R., Santos J.L., Cabezas M.P., Sequeira F. & Santos A.M. 2025. Genetic analysis of Pinna rudis L 1758 (Mollusca, Bivalvia, Pinnidae) in the Northwest Cabo Verde Islands (Central-East Atlantic). PeerJ 13: e18328. DOI:10.7717/peerj.18328
???msg.biblio.abstract.label??? [+] [-]The rough pen shell Pinna rudis Linnaeus, 1758 (family Pinnidae) is a mollusc with an Atlantic–Mediterranean distribution, typically inhabiting coarse sandy substrates. Habitat degradation is considered the primary cause of population decline, leading to the designation ‘Vulnerable’ in certain regions. In this study, we conducted a genetic analysis of populations of P. rudis from Cabo Verde and compared them with populations from the Mediterranean and Macaronesia. We based our analysis on two mitochondrial DNA markers, cytochrome oxidase I (COI) and 16S rRNA, and one nuclear marker, 28S rRNA. The results showed a strong genetic structuring among Macaronesia populations, with each island tending to have unique or exclusive haplotypes, though some sharing occurred between islands. We found significant genetic divergence between the population from Cabo Verde and the other sampled population, suggesting that P. rudis is not monotypic, but may include several cryptic species. Bayesian and maximum-likelihood phylogenetic analysis, including all Pinnidae species, indicated that P. rudis from Gorée Island (Senegal) and Baía das Gatas (São Vicente Island) might be undergoing speciation. The high genetic structure found for P. rudis could be influenced by hydrodynamic barriers, local currents and hydrographic isolation, in association with the short larval duration (planktotrophic) reported for this species. Altogether, our findings highlight significant genetic divergence in P. rudis populations, possibly supporting speciation events in the Cabo Verde archipelago among widely distributed taxonomic groups.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]BIOPAPUA, CONCALIS, ???msg.security.private???, EXBODI, INHACA 2011, KARUBENTHOS 2012, PAKAIHI I TE MOANA, ???msg.security.private???
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Lozouet P. & Galindo L.A. 2015. Resolution of the confused classification of some Miocene Nassariidae, and reappraisal of their paleobiodiversity on the French Atlantic seaboard. Archiv für Molluskenkunde 144(1): 31-50. DOI:10.1127/arch.moll/1869-0963/144/031-050
???msg.biblio.biblioSurvey.label??? (4) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Mah C.L. 2017. Overview of the Ferdina-like Goniasteridae (Echinodermata: Asteroidea) including a new subfamily, three new genera and fourteen new species. Zootaxa 4271(1): 1-72. DOI:10.11646/zootaxa.4271.1.1
???msg.biblio.biblioSurvey.label??? (24) [+] [-]ATIMO VATAE, AZTEQUE, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, BIOCAL, BORDAU 1, BORDAU 2, CHALCAL 2, CONCALIS, EBISCO, EXBODI, LITHIST, MIRIKY, MUSORSTOM 4, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, SALOMON 2, SMIB 3, SMIB 4, SMIB 5, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
Mah C.L. 2021. The East Pacific/South Pacific Boundary: New taxa and occurrences from Rapa Nui (Easter Island), New Caledonia and adjacent regions. Zootaxa 4980(3): 401-450. DOI:10.11646/zootaxa.4980.3.1
???msg.biblio.abstract.label??? [+] [-]Recent expeditions to Rapa Nui (also known as Easter Island) and New Caledonia have revealed undescribed species from mesophotic and deeper depths. This includes three new species from Rapa Nui, Hacelia raaraa, Linckia profunda (Ophidiasteridae), Uokeaster ahi (Asterodiscididae) and two new species from New Caledonia, Astroglypha pyramidata n. gen. and Ophidiaster colossus (Ophidiasteridae). The new genus Astroglypha is described for A. pyramidata but the genus also includes the Atlantic Tamaria passiflora, which is reassigned herein. Pauliastra n. gen. is designated as a replacement for the homonym issue with Pauliella. New occurrences and synonymies are addressed for taxa related to New Caledonia, Rapa Nui and adjacent regions. A morphology based phylogenetic analysis agrees with prior work which placed Goniaster among the Asterodiscididae and posits biogeographic relationships among asterodiscidid genera. Implications for the Goniasteridae and placement of Goniaster among asterodiscidid genera are discussed. Biogeography and relationships among taxa from Rapa Nui and New Caledonia are reviewed. In situ observations from species observed from Rapa Nui are included.
???msg.biblio.biblioSurvey.label??? (16) [+] [-]AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, EXBODI, HALIPRO 1, KANACONO, KANADEEP, LITHIST, MUSORSTOM 10, MUSORSTOM 4, NORFOLK 1, ???msg.security.private???, SMIB 4
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
Messing C.G. 2013. A revision of the genus Atelecrinus PH Carpenter (Echinodermata: Crinoidea). Zootaxa 3681(1): 1-43. DOI:10.11646/zootaxa.3681.1.1
???msg.biblio.abstract.label??? [+] [-]The unusual bathyal comatulid crinoid genus Atelecrinus is widespread in the Atlantic and tropical Pacific Oceans and currently includes three recognized species. A re-assessment based on examination of new and existing specimens requires establishment of two new genera and five new species, and returns three junior synonyms to species-level status. Paratelecrinus is erected to accommodate Atelecrinus wyvilli PH Carpenter, A. conifer AH Clark, A. cubensis PH Carpenter, P. orthotriremis, new species, P. amenouzume new species, P. laticonulus new species and P. telo new species. Adelatelecrinus is erected to accommodate Atelecrinus sulcatus AH Clark and Adelatelecrinus vallatus new species. Atelecrinus retains A. balanoides PH Carpenter and A. helgae AH Clark, which restricts the genus to the Atlantic. In both Paratelecrinus and Adelatelecrinus, the basals articulate with the centrodorsal via ligament bundles anchored in deep ring-like interradial pits that project into the centrodorsal cavity, whereas in Atelecrinus the centrodorsal rim has shallow interradial concavities and attaches to the basals via a tight junction with no obvious ligament bundles. The spoon-shaped aboral fossa in the basals of Paratelecrinus appears to be unique among articulate crinoids and differs from the smooth fossa found in both Atelecrinus and Adelatelecrinus. New material extends the range of the family to the Indian Ocean. A few species are now known from enough specimens to identify some ontogenetic and distributional variations. Proximal ray morphology varies substantially with size in P. cubensis and P. orthotriremis. A. balanoides generally occurs in deeper water in the Lesser Antilles than in the Bahamas and Strait of Florida, while P. orthotriremis occurs in shallower water in the Lesser Antilles and deeper in the Bahamas.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
Messing C.G. & Romanowski A. 2022. A Revision Of The Feather Star Genera Poecilometra and Strotometra (Echinodermata: Crinoidea: Charitometridae). Contributions from the Museum of Paleontology, University of Michigan 34(12): 158-192. DOI:10.7302/4815
???msg.biblio.abstract.label??? [+] [-]The chiefly tropical, deep-water (>100 m) feather star family Charitometridae (Echinodermata: Crinoidea: Comatulida) currently consists of 34 species in eight genera and has not been revised since 1950. Recent molecular analyses and the discovery of both new specimens of known species and a new species prompted a morphological re-examination of those genera with abruptly expanded genital pinnules. As a result, Poecilometra is redescribed, and now includes four species, including two formerly placed in Strotometra, plus Poecilometra baumilleri n. sp Poecilometra scalaris is placed in synonymy under P. acoela. Strotometra is redescribed and S. hepburniana placed in synonymy under S. parvipinna. The diagnoses of both genera and their component species are revised.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Modica M.V., Puillandre N., Castelin M., Zhang Y. & Holford M. 2014. A Good Compromise: Rapid and Robust Species Proxies for Inventorying Biodiversity Hotspots Using the Terebridae (Gastropoda: Conoidea), in Kolokotronis S.O. (Ed.), PLoS ONE 9(7): e102160. DOI:10.1371/journal.pone.0102160
???msg.biblio.abstract.label??? [+] [-]Devising a reproducible approach for species delimitation of hyperdiverse groups is an ongoing challenge in evolutionary biology. Speciation processes combine modes of passive and adaptive trait divergence requiring an integrative taxonomy approach to accurately generate robust species hypotheses. However, in light of the rapid decline of diversity on Earth, complete integrative approaches may not be practical in certain species-rich environments. As an alternative, we applied a two-step strategy combining ABGD (Automated Barcode Gap Discovery) and Klee diagrams, to balance speed and accuracy in producing primary species hypotheses (PSHs). Specifically, an ABGD/Klee approach was used for species delimitation in the Terebridae, a neurotoxin-producing marine snail family included in the Conoidea. Delimitation of species boundaries is problematic in the Conoidea, as traditional taxonomic approaches are hampered by the high levels of variation, convergence and morphological plasticity of shell characters. We used ABGD to analyze gaps in the distribution of pairwise distances of 454 COI sequences attributed to 87 morphospecies and obtained 98 to 125 Primary Species Hypotheses (PSHs). The PSH partitions were subsequently visualized as a Klee diagram color map, allowing easy detection of the incongruences that were further evaluated individually with two other species delimitation models, General Mixed Yule Coalescent (GMYC) and Poisson Tree Processes (PTP). GMYC and PTP results confirmed the presence of 17 putative cryptic terebrid species in our dataset. The consensus of GMYC, PTP, and ABGD/Klee findings suggest the combination of ABGD and Klee diagrams is an effective approach for rapidly proposing primary species proxies in hyperdiverse groups and a reliable first step for macroscopic biodiversity assessment.
???msg.biblio.biblioSurvey.label??? (13) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, BOA1, EBISCO, EXBODI, MIRIKY, PANGLAO 2004, PANGLAO 2005, SALOMON 2, SANTO 2006, TERRASSES, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Neiber M.T. & Glaubrecht M. 2019. Oligohalinophila , a new genus for the brackish water assassin snail Canidia dorri Wattebled, 1886 from Vietnam (Buccinoidea: Nassariidae: Anentominae). Journal of Molluscan Studies. DOI:10.1093/mollus/eyy065
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Ng P.K.L. & Castro P. 2020. A revision of Carcinoplax abyssicola (Miers, 1885) and seven related species of Carcinoplax H. Milne Edwards, 1852, with the description of two new species and an updated key to the genus (Crustacea, Decapoda, Brachyura, Goneplacidae). Zoosystema 42(17): 239-284. DOI:10.5252/zoosystema2020v42a17
???msg.biblio.abstract.label??? [+] [-]The identities of the deep-water brachyuran crabs Carcinoplax abyssicola (Miers, 1885), C. longipes (Wood-Mason, 1891), and C. specularis Rathbun, 1914 (family Goneplacidae MacLeay, 1838) are clarified on the basis of the examination of types and of an extensive series of specimens from the Indo-West Pacific region, including colour photographs of fresh specimens. Two species described from the Philippines, C. verdensis Rathbun, 1914 and C. polita Guinot, 1989, and previously synonymised under C. specularis, are shown to be distinct species. Two new species, C. adelphia n. sp. and C. jugum n. sp., are described from Vanuatu and the Philippines, respectively. Carcinoplax adelphia n. sp. differs from the closely allied C. specularis by having a male first gonopod (G1) that is relatively more elongated, particularly the distinctly more slender distal half, than the G1 of C. specularis. Carcinoplax jugum n. sp. is characterized by a suite of characters that includes an epistome with strongly concave lateral margins, a carapace having distinctly swollen gastric and cardiac regions, and a G1 with a subconical distal part. The taxonomies of these seven species, as well as that of the allied C. fasciata Ng & Kumar, 2016 from southwestern India, are revised. A revised, updated key to the 25 known species of Carcinoplax H. Milne Edwards, 1852 is also provided.
???msg.biblio.biblioSurvey.label??? (20) [+] [-]BATHUS 4, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, EXBODI, KARUBAR, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 3, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 6, TAIWAN 2001, TARASOC
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K.L. & Forges B.R.D. 2021. A new species of spider crab of the genus Sakaija (Brachyura: Majidae) from New Caledonia. Crustacean Research 50(0): 95-101. DOI:10.18353/crustacea.50.0_95
???msg.biblio.abstract.label??? [+] [-]A new species of majid crab, Sakaija amicitiae n. sp., is described from New Caledonia Exclusive Economic Zone, Vauban seamount and the Chesterfield Atolls. The species is superficially similar to S. japonica (Rathbun, 1932) and S. santo Ng & Richer de Forges, 2015, from Vanuatu. Specimens from New Caladonia previously referred to S. santo are now referred to the new species. Sakaija amicitiae n. sp. can be distinguished from congeners by features of the carapace spines, proportions of the ambulatory legs and structure of the male first gonopod.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K. & Richer de Forges B. 2013. Samadinia longispina, a new genus and species of deep-sea spider crab from the western Pacific, and a new species of Rochinia A. Milne-Edwards, 1875, from Papua New Guinea (Crustacea: Brachyura: Majoidea: Epialtidae). Zootaxa 3718(4): 357. DOI:10.11646/zootaxa.3718.4.5
???msg.biblio.abstract.label??? [+] [-]A new genus, Samadinia n. gen., and new species, Samadinia longispina n. sp., of deep-water epialtid spider crab is described from French Polynesia and New Caledonia. The new genus is superficially similar to Rochinia A. Milne-Edwards, 1875, but can be distinguished by having the dorsal surface of the carapace covered with small, rounded granules (versus with long spines or strong tubercles), well developed hepatic and lateral branchial spines (versus relatively shorter and weaker), a prominently constricted male thoracic sternite 4 (versus relatively broader with less prominent or without median constriction) and a proportionally broader male abdomen. A new species of Rochinia, R. granulosa n. sp., is also described from Papua New Guinea. It is easily distinguished from congeners its small adult size, the presence of numerous relatively large granules on the carapace and a relatively short hepatic spine.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K. & Richer de Forges B. 2015. Revision of the spider crab genus Maja Lamarck, 1801 (Crustacea: Brachyura: Majoidea: Majidae), with descriptions of seven new genera and 17 new species from the Atlantic and Indo-West Pacific. Raffles Bulletin of Zoology 63: 110-225
???msg.biblio.abstract.label??? [+] [-]The taxonomy of spider crabs of the genus Maja Lamarck, 1801, is revised, and a total of 36 species in 10 genera are now recognised from the eastern Atlantic, Mediterranean and Indo-West Pacific. The present revision describes seven genera and 17 species as new. Two genera previously synonymised under Maja: Paramaya De Haan, 1837, and Paramaja Kubo, 1936, are here treated as valid taxa. The confused nomenclature of Cancer cornutus Linnaeus, 1758, is resolved, and the name replaces Maja capensis Ortmann, 1894, and Mamaia queketti Stebbing, 1908. All genera and species are diagnosed and figured, and keys are provided for their identification.
???msg.biblio.biblioSurvey.label??? (12) [+] [-]AURORA 2007, BIOPAPUA, EBISCO, EXBODI, MIRIKY, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, PANGLAO 2005, SALOMON 1, SALOMON 2, SANTO 2006
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Ng P.K. & Castro P. 2016. Revision of the family Chasmocarcinidae Serène, 1964 (Crustacea, Brachyura, Goneplacoidea). Zootaxa 4209(1): 1-182. DOI:10.11646/zootaxa.4209.1.1
???msg.biblio.abstract.label??? [+] [-]The family Chasmocarcinidae Serène, 1964, is revised based on the examination of the type material of many of its species as well as unidentified and previously identified material from around the world. The revised family now consists of three subfamilies comprising 16 genera (including eight described as new) and 51 species (including 19 described as new). The subfamily Chasmocarciinae Serène, 1964, consists of Amboplax n. gen. with one species; Angustopelta n. gen. with four species, two of which are new; Camatopsis Alcock & Anderson, 1899, with six species, five of which are new; Chasmocarcinops Alcock, 1900, with one species; Chasmocarcinus Rathbun, 1898, with 11 species, one of which is new; Chinommatia n. gen. with five species, two of which are new; Deltopelta n. gen. with one species; Hephthopelta Alcock, 1899, with two species, one of which is new; Microtopsis Komai, Ng & Yamada, 2012, with two species, one of which is new; Notopelta n. gen. with one species; Statommatia n. gen. with five species, two of which are new; and Tenagopelta n. gen. with three species, two of which are new. The subfamily Megaesthesiinae Števčić, 2005, consists of Alainthesius n. gen. with two species, both of which are new; Megaesthesius Rathbun, 1909, with four species, one of which is new. The subfamily Trogloplacinae Guinot, 1986, consists of Australocarcinus Davie, 1988, with three species, and Trogloplax Guinot, 1986, with one species. A neotype is selected for Chasmocarcinus cylindricus Rathbun, 1901. Three nominal species were found to be junior subjective synonyms of other species: Chasmocarcinus panamensis Serène, 1964, of C. longipes Garth, 1940; Chasmocarcinus rathbuni Bouvier, 1917, of C. typicus Rathbun, 1898; and Hephthopelta superba Boone, 1927, of Deltopelta obliqua (Rathbun, 1898). Thirteen chasmocarcinid genera are exclusively found in the Indo-West Pacific region, one (Chasmocarcinus) in both the Western Atlantic and Tropical Eastern Pacific regions, and two (Deltopelta n. gen. and Amboplax n. gen.) exclusively in the Western Atlantic. Chasmocarcinids are remarkable for occurring from depths exceeding 1000 m to shallow water and completely freshwater habitats: chasmocarcinines and megaesthesiines are found from shallow to deep water marine ecosystems, whereas trogloplacines live in freshwater streams, including cave systems.
???msg.biblio.biblioSurvey.label??? (29) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 4, BIOPAPUA, BOA1, BORDAU 1, ???msg.security.private???, CORINDON 2, EXBODI, HALIPRO 1, KARUBAR, KARUBENTHOS 2012, MAINBAZA, MIRIKY, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 8, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMONBOA 3, SANTO 2006
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Nocella E., Fassio G., Zuccon D., Puillandre N., Modica M.V. & Oliverio M. 2024. From coral reefs into the abyss: the evolution of corallivory in the Coralliophilinae (Neogastropoda, Muricidae). Coral Reefs 43(5): 1285-1302. DOI:10.1007/s00338-024-02537-1
???msg.biblio.abstract.label??? [+] [-]In this study, we delved into the interaction between corallivorous marine gastropods, the muricid Coralliophilinae Chenu, 1859, and their cnidarian food targets. Coralliophilinae is a subfamily of specialised corallivorous caenogastropods that feed by browsing on octocorals or hexacorals. Only sparse information is available on the phylogenetic relationships and the degree of specificity of the trophic relationships within this corallivorous lineage. To address these gaps, we generated the largest molecular dataset to date, comprising two mitochondrial (cox1 and 16S rDNA) and one nuclear gene (ITS2 rDNA) from 586 specimens collected worldwide. The coral hosts of coralliophilines were identified through an integrative approach, combining literature data with new records, employing morphological and/or molecular markers, and incorporating data from DNA barcoding of the snail stomach content. Our comprehensive approach unveiled the existence of numerous cryptic species in Coralliophilinae, while the phylogeny showed that most of the currently accepted genera are not monophyletic. The molecular dating confirmed the origin of the Coralliophilinae in Middle Eocene, with diversification of most lineages during the Miocene. Our results indicate that the subfamily’s ancestor evolved in shallow waters in association with Scleractinia. Through the evolutionary history of Coralliophilinae, multiple host shifts to other cnidarian orders were observed, not correlated with changes in the depth range. The results of diversification analyses within the subfamily further suggest that the association with the host has influenced the evolutionary patterns of Coralliophilinae, but not vice versa.
???msg.biblio.biblioSurvey.label??? (27) [+] [-]ATIMO VATAE, BIOMAGLO, CONCALIS, CORSICABENTHOS 2, CORSICABENTHOS 3, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KAVIENG 2014, LIFOU 2000, MADIBENTHOS, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SANTO 2006, TARASOC, TERRASSES, Tuhaa Pae 2013, Walters Shoal, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
O'Hara T.D., Thuy B. & Hugall A.F. 2021. Relict from the Jurassic: new family of brittle-stars from a New Caledonian seamount. Proceedings of the Royal Society B: Biological Sciences 288(1953): 20210684. DOI:10.1098/rspb.2021.0684
???msg.biblio.abstract.label??? [+] [-]The deep-seafloor in the tropical Indo-Pacific harbours a rich and diverse benthic fauna with numerous palaeoendemics. Here, we describe a new species, genus and family of brittle-star (Ophiuroidea) from a single eight-armed specimen collected from a depth between 360 and 560 m on Banc Durand, a seamount east of New Caledonia. Leveraging a robust, fossil-calibrated (265 kbp DNA) phylogeny for the Ophiuroidea, we estimate the new lineage diverged from other ophiacanthid families in the Late Triassic or Jurassic (median = 187–178 Myr, 95% CI = 215–143 Myr), a period of elevated diversification for this group. We further report very similar microfossil remains from Early Jurassic (180 Myr) sediments of Normandy, France. The discovery of a new ancient lineage in the relatively well-known Ophiuroidea indicates the importance of ongoing taxonomic research in the deep-sea, an environment increasingly threatened by human activities.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
Ogino A., Lee S.H., Chen W.J. & Matsunuma M. 2020. Chelidoperca cerasina sp. nov., a new perchlet (Perciformes: Serranidae) from the southwest Pacific Ocean. Ichthyological Research 67(1): 117-132. DOI:10.1007/s10228-019-00714-9
???msg.biblio.abstract.label??? [+] [-]The new serranid fish Chelidoperca cerasina is described on the basis of 13 specimens from the Coral Sea (off New Caledonia and eastern Australia), southwest Pacific Ocean, at depths of 245–338 m. The new species can be readily distinguished from all congeners by having the following combination of characters: an orange spot on pectoral-fin and caudal-fin bases; 4 scale rows between lateral line and base of spinous dorsal fin; cheek scales in 8 or 9 (modally 8) rows; tip of upper caudal-fin lobe elongated, slightly longer than lower lobe in specimens > ca. 100 mm; no longitudinal dark stripe or row of dark blotches laterally on body; interorbital scales extending beyond mid-orbit level, but not reaching anterior margin of orbit; scales on ventral surface of lower jaw restricted to angular, absent on dentary; pelvic fin short, tip not reaching anus when adpressed.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IC (Ichtyologie) -
Pante E., Heestand Saucier E. & France S.C. 2013. Molecular and morphological data support reclassification of the octocoral genus Isidoides. Invertebrate Systematics 27(4): 365-378. DOI:10.1071/IS12053
???msg.biblio.abstract.label??? [+] [-]The rare octocoral genus Isidoides Nutting, 1910 was originally placed in the Gorgonellidae (now the Ellisellidae), even though it showed a remarkable similarity to the Isidae (now the Isididae). Isidoides was not classified in the Isididae mostly because the type specimen lacked skeletal nodes, a defining characteristic of that family. The genus was later assigned to the Chrysogorgiidae based on sclerite morphology. Specimens were recently collected in the south-western Pacific, providing material for genetic analysis and detailed characterisation of the morphology, and allowing us to consider the systematic placement of this taxon within the suborder Calcaxonia.Apreviously reported phylogeny allowed us to reject monophyly with the Chrysogorgiidae, and infer a close relationship with the Isididae subfamily Keratoisidinae. While scanning for molecular variation across mitochondrial genes, we discovered a novel gene order that is, based on available data, unique among metazoans. Despite these new data, the systematic placement of Isidoides is still unclear, as (1) the phylogenetic relationships among Isididae subfamilies remain poorly resolved, (2) genetic distances between mitochondrial mtMutS sequences from Isidoides and Keratoisidinae are characteristic of intra-familial distances, and (3) mitochondrial gene rearrangements may occur among confamilial genera. For these reasons, and because a revision of the Isididae is beyond the scope of this contribution, we amend the familial placement of Isidoides to incertae sedis.
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
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) -
Peñas A. & Rolan E. 2016. Deep water Pyramidelloidea from the Central and South Pacific: 3. The Tribes Eulimellini and Syrnolini ISBN:978-84-16533-79-4
???msg.biblio.biblioSurvey.label??? (23) [+] [-]AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BIOCAL, BOA1, BORDAU 2, CONCALIS, EXBODI, LAGON, MUSORSTOM 10, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PANGLAO 2005, SALOMON 1, SALOMON 2, SANTO 2006, SMIB 8, VAUBAN 1978-1979
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Poppe G.T., Tagaro S.P. & HUANG S.I. 2023. The Recent Colloniidae. ConcBooks, Harxheim, Germany, 372 pp.
???msg.biblio.biblioSurvey.label??? (39) [+] [-]ATIMO VATAE, AURORA 2007, BATHUS 1, BATHUS 2, BENTHAUS, BERYX 11, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, CONCALIS, EBISCO, EXBODI, KARUBAR, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, LIFOU 2000, MAINBAZA, MONTROUZIER, MUSORSTOM 10, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 1, SALOMON 2, SALOMONBOA 3, SMIB 8, TAIWAN 2000, TARASOC, Tuhaa Pae 2013, ???msg.security.private???
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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) -
Rodríguez Flores P.C. & Schnabel K.E. 2023. New records and species of deep-sea squat lobsters (Galatheoidea, Munidopsidae) from the Hawaiian Archipelago: an integrative approach using micro-CT and barcodes. PeerJ 11: e14956. DOI:10.7717/peerj.14956
???msg.biblio.abstract.label??? [+] [-]The Hawaiian Archipelago remains extensively under-sampled for many marine invertebrate taxa, including squat lobsters. During the last few years, several deep-sea expeditions carried out in the Pacific Ocean have conducted opportunistic collections of specimens and image data from the vicinity of Hawai’i. Here we describe a new species: Munidopsis hawaii sp. nov. and provide new records for Munidopsidae in the Archipelago and its associations. We illustrate and describe the new species using an integrative approach including micro-CT 3D imaging. Phylogenetic analyses of the species collected from seamounts from Hawai’i indicate that the new species represents a divergent lineage compared to morphologically similar species such as M. dispar and M. papanui. We also study the genetic distances for the species recorded in Hawai’i and other populations of the same species in the adjacent West Pacific. Three species are now known in the Hawaiian region. We also compiled identifications from images captured with ROVs in the area. These observations suggest that munidopsid species are common in the deep sea of Hawaiian waters below 1,000 m.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rodríguez-Flores P., Macpherson E., Schnabel K., Ahyong S., Corbari L. & Machordom A. 2022. Depth as a driver of evolution and diversification of ancient squat lobsters (Decapoda, Galatheoidea, Phylladiorhynchus). Molecular Phylogenetics and Evolution 171: 107467. DOI:10.1016/j.ympev.2022.107467
???msg.biblio.biblioSurvey.label??? (34) [+] [-]ATIMO VATAE, BENTHAUS, BIOMAGLO, BIOPAPUA, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBAR, KAVIENG 2014, KOUMAC 2.3, LAGON, LIFOU 2000, MD08 (BENTHOS), MD32 (REUNION), MONTROUZIER, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, PAKAIHI I TE MOANA, PALEO-SURPRISE, PAPUA NIUGINI, RAPA 2002, SANTO 2006, TARASOC, Walters Shoal
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Rodríguez-Flores P.C., Macpherson E. & Machordom A. 2021. Revision of the squat lobsters of the genus Phylladiorhynchus Baba, 1969 (Crustacea, Decapoda, Galatheidae) with the description of 41 new species. Zootaxa 5008(1): 1-159. DOI:10.11646/zootaxa.5008.1.1
???msg.biblio.abstract.label??? [+] [-]The genus Phylladiorhynchus Baba, 1969 currently contains 11 species, all occurring in the shallow waters and on the continental shelf of the Indian and Pacific oceans. Recent expeditions in these oceans have resulted in the collection of numerous new specimens in need of analysis. We have studied this material using an integrative approach analysing both morphological and molecular (COI and 16S) characters. We describe 41 new species and resurrect three old names: P. integrus (Benedict, 1902) and P. lenzi (Rathbun, 1907), previously synonymized with P. pusillus (Henderson, 1885), and P. serrirostris (Melin, 1939), previously synonymized with P. integrirostris (Dana, 1852). Most species of the genus are described and illustrated. Some species are barely discernible on the basis of morphological characters but are highly divergent genetically. Species of Phylladiorhynchus are mainly distinguishable by the number of epigastric spines and lateral spines of the carapace, the shape and the armature of the rostrum, the number and pattern of the ridges on the carapace and pleon, the shape of thoracic sternite 3 and the armature of the P2–4 dactyli. A dichotomous identification key to all species is provided.
???msg.biblio.biblioSurvey.label??? (35) [+] [-]ATIMO VATAE, BENTHAUS, BIOMAGLO, BIOPAPUA, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBAR, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, LAGON, LIFOU 2000, MD08 (BENTHOS), MD32 (REUNION), MONTROUZIER, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, PAKAIHI I TE MOANA, PALEO-SURPRISE, PAPUA NIUGINI, RAPA 2002, SANTO 2006, TARASOC, Walters Shoal
???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. 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) -
Sabroux R., Corbari L. & Hassanin A. 2023. Phylogeny of sea spiders (Arthropoda: Pycnogonida) inferred from mitochondrial genome and 18S ribosomal RNA gene sequences. Molecular Phylogenetics and Evolution 182: 107726. DOI:10.1016/j.ympev.2023.107726
???msg.biblio.abstract.label??? [+] [-]The phylogeny of sea spiders has been debated for more than a century. Despite several molecular studies in the last twenty years, interfamilial relationships remain uncertain. In the present study, relationships within Pyc nogonida are examined in the light of a new dataset composed of 160 mitochondrial genomes (including 152 new sequences) and 130 18S rRNA gene sequences (including 120 new sequences), from 141 sea spider mor phospecies representing 26 genera and 9 families. Node congruence between mitochondrial and nuclear markers was analysed to identify the most reliable relationships. We also reanalysed a multilocus dataset previously published and showed that the high percentages of missing data make phylogenetic conclusions difficult and uncertain.
???msg.biblio.biblioSurvey.label??? (23) [+] [-]ATIMO VATAE, BICOSE, BIOCAL, BIOMAGLO, BIOPAPUA, CEAMARC-AA, EXBODI, GUYANE 2014, ILES DU SALUT, KANACONO, KANADEEP, KARUBENTHOS 2012, KAVIENG 2014, MADIBENTHOS, MAINBAZA, MIRIKY, MONTROUZIER, MUSORSTOM 4, MUSORSTOM 8, PAPUA NIUGINI, SALOMONBOA 3, TARASOC, Walters Shoal
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Sanders M.T., Merle D., Laurin M., Bonillo C. & Puillandre N. 2021. Raising names from the dead: A time-calibrated phylogeny of frog shells (Bursidae, Tonnoidea, Gastropoda) using mitogenomic data. Molecular Phylogenetics and Evolution 156: 107040. DOI:10.1016/j.ympev.2020.107040
???msg.biblio.abstract.label??? [+] [-]With 59 Recent species, Bursidae, known as «frog shells», are a small but widely distributed group of tropical and subtropical gastropods that are most diverse in the Indo-West Pacific. The present study is aimed at recon structing phylogenetic relationships of bursid gastropods based on extensive and representative taxon sampling. Five genetic markers (cytochrome c oxidase subunit I (cox1), 16 s and 12 s rRNA mitochondrial genes, 28 s rRNA and Histone H3 nuclear gene) were sequenced for over 30 species in every known genus but Crossata. Furthermore, we sequenced the complete mt-genome of 9 species (10 specimens) (Aspa marginata, Marsupina bufo, Korrigania quirihorai, Korrigania fijiensis, Tutufa rubeta, Bursa lamarckii, Lampasopsis rhodostoma (twice), Bufonaria perelegans and Bursa aff. tuberosissima). Our analysis recovered Bursidae as a monophyletic group, whereas the genus Bursa was found to be polyphyletic. The genera Talisman and Dulcerana are resurrected and the genera Alanbeuella gen. nov. and Korrigania gen. nov. are described. Dating analysis using 21 extinct taxa for node and simplified tip calibrations was performed, showing a diversification of the group in two phases. Diversification may be linked to tectonic events leading to biodiversity relocation from the western Tethys to ward the Indo-Pacific.
???msg.biblio.biblioSurvey.label??? (22) [+] [-]ATIMO VATAE, CONCALIS, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, MAINBAZA, MIRIKY, NORFOLK 1, NORFOLK 2, PAKAIHI I TE MOANA, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006, TERRASSES, Tuhaa Pae 2013, ???msg.security.private???, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Saucier E.H., France S.C. & Watling L. 2021. Toward a revision of the bamboo corals: Part 3, deconstructing the Family Isididae. Zootaxa 5047(3): 247-272. DOI:10.11646/zootaxa.5047.3.2
???msg.biblio.abstract.label??? [+] [-]Bamboo corals are distinguished from most other octocorals by an articulated skeleton. The nodes are proteinaceous and sclerite-free while the internodes are composed of non-scleritic calcium carbonate. This articulation of the skeleton was thought to be unique and a strong synapomorphy for the family Isididae. Our phylogeny, based on the amplification of mtMutS and 18S, shows an articulating skeleton with sclerite-free nodes has arisen independently at least five times during the evolutionary history of Octocorallia rather than being a synapomorphy characteristic of a monophyletic bamboo coral clade. The family Isididae is currently composed of four subfamilies (Circinisidinae, Isidinae, Keratoisidinae, and Mopseinae). Not only is the family polyphyletic, but our genetic analyses suggest also the subfamily Isidinae is polyphyletic based on current taxonomic classifications, and Mopseinae is not monophyletic. The type, Isis, is found outside of the well-supported Calcaxonia – Pennatulacea clade where the other members of Isididae cluster. The current classification of the family Isididae does not reflect the evolutionary history of an articulated skeleton. To better reflect the evolutionary history of these taxa we propose that three of the four the subfamilies, the genus Isidoides, and genera within the subfamily Isidinae, be elevated to family level to produce a classification with five families with a bamboo-like skeleton: Chelidonisididae, Isididae, Isidoidae, Keratoisididae, and Mopseidae.
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
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) -
Sirenko B.I. 2021. Restoration of the genus Squamophora (Mollusca: Polyplacophora: Loricidae). Ruthenica: 51-58
???msg.biblio.abstract.label??? [+] [-]I propose to restore the old genus name Squamophora for S. oviformis and the described herein S. nierstraszi sp. nov.. A new emendation of the genus Squamophora is provided, taking into account the main features of the shell, girdle and radula that distinguish it from the closely-related genus Loricella. The new species differs from the type species by the sculpture of the dorsal scales and the shape of the radula teeth
???msg.biblio.biblioSurvey.label??? (2) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Strong E.E., Galindo L.A. & Kantor Y.I. 2017. Quid est Clea helena? Evidence for a previously unrecognized radiation of assassin snails (Gastropoda: Buccinoidea: Nassariidae). PeerJ 5: e3638. DOI:10.7717/peerj.3638
???msg.biblio.abstract.label??? [+] [-]The genus Clea from SE Asia is from one of only two unrelated families among the megadiverse predatory marine Neogastropoda to have successfully conquered continental waters. While little is known about their anatomy, life history and ecology, interest has grown exponentially in recent years owing to their increasing popularity as aquarium pets. However, the systematic affinities of the genus and the validity of the included species have not been robustly explored. Differences in shell, operculum and radula characters support separation of Clea as presently defined into two distinct genera: Clea, for the type species Clea nigricans and its allies, and Anentome for Clea helena and allies. A five-gene mitochondrial (COI, 16S, 12S) and nuclear (H3, 28S) gene dataset confirms the placement of Anentome as a somewhat isolated offshoot of the family Nassariidae and sister to the estuarine Nassodonta. Anatomical data corroborate this grouping and, in conjunction with their phylogenetic placement, support their recognition as a new subfamily, the Anentominae. The assassin snail Anentome helena, a popular import through the aquarium trade so named for their voracious appetite for other snails, is found to comprise a complex of at least four species. None of these likely represents true Anentome helena described from Java, including a specimen purchased through the aquarium trade under this name in the US and one that was recently found introduced in Singapore, both of which were supported as conspecific with a species from Thailand. The introduction of Anentome “helena” through the aquarium trade constitutes a significant threat to native aquatic snail faunas which are often already highly imperiled. Comprehensive systematic revision of this previously unrecognized species complex is urgently needed to facilitate communication and manage this emerging threat.
???msg.biblio.biblioSurvey.label??? (9) [+] [-]ATIMO VATAE, BIOPAPUA, EXBODI, INHACA 2011, KARUBENTHOS 2012, MAINBAZA, PANGLAO 2004, ???msg.security.private???, SANTO 2006
???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) -
Sumner-Rooney L., Sigwart J.D., McAfee J., Smith L. & Williams S.T. 2016. Repeated eye reduction events reveal multiple pathways to degeneration in a family of marine snails: EYE REDUCTION IN A FAMILY OF MARINE SNAILS. Evolution 70(10): 2268-2295. DOI:10.1111/evo.13022
???msg.biblio.abstract.label??? [+] [-]Eye reduction occurs in many troglobitic, fossorial, and deep-sea animals but there is no clear consensus on its evolutionary mechanism. Given the highly conserved and pleiotropic nature of many genes instrumental to eye development, degeneration might be expected to follow consistent evolutionary trajectories in closely related animals. We tested this in a comparative study of ocular anatomy in solariellid snails from deep and shallow marine habitats using morphological, histological, and tomographic techniques, contextualized phylogenetically. Of 67 species studied, 15 lack retinal pigmentation and at least seven have eyes enveloped by surrounding epithelium. Independent instances of reduction follow numerous different morphological trajectories. We estimate eye loss has evolved at least seven times within Solariellidae, in at least three different ways: characters such as pigmentation loss, obstruction of eye aperture, and “lens” degeneration can occur in any order. In one instance, two morphologically distinct reduction pathways appear within a single genus, Bathymophila. Even amongst closely related animals living at similar depths and presumably with similar selective pressures, the processes leading to eye loss have more evolutionary plasticity than previously realized. Although there is selective pressure driving eye reduction, it is clearly not morphologically or developmentally constrained as has been suggested by previous studies.
???msg.biblio.biblioSurvey.label??? (18) [+] [-]AURORA 2007, BIOPAPUA, BOA1, CONCALIS, EBISCO, EXBODI, KARUBENTHOS 2012, MAINBAZA, MIRIKY, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006, TAIWAN 2001, TARASOC, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Sumner-Rooney L., Kenny N.J., Ahmed F. & Williams S.T. 2019. The utility of micro-computed tomography for the non-destructive study of eye microstructure in snails. Scientific Reports 9(1): 15411. DOI:10.1038/s41598-019-51909-z
???msg.biblio.abstract.label??? [+] [-]Abstract Molluscan eyes exhibit an enormous range of morphological variation, ranging from tiny pigment-cup eyes in limpets, compound eyes in ark clams and pinhole eyes in Nautilus , through to concave mirror eyes in scallops and the large camera-type eyes of the more derived cephalopods. Here we assess the potential of non-destructive micro-computed tomography (µ-CT) for investigating the anatomy of molluscan eyes in three species of the family Solariellidae, a group of small, deep-sea gastropods. We compare our results directly with those from traditional histological methods applied to the same specimens, and show not only that eye microstructure can be visualised in sufficient detail for meaningful comparison even in very small animals, but also that μ-CT can provide additional insight into gross neuroanatomy without damaging rare and precious specimens. Data from μ-CT scans also show that neurological innervation of eyes is reduced in dark-adapted snails when compared with the innervation of cephalic tentacles, which are involved in mechanoreception and possibly chemoreception. Molecular tests also show that the use of µ-CT and phosphotungstic acid stain do not prevent successful downstream DNA extraction, PCR amplification or sequencing. The use of µ-CT methods is therefore highly recommended for the investigation of difficult-to-collect or unique specimens.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Takano T. & Kano Y. 2014. Molecular phylogenetic investigations of the relationships of the echinoderm-parasite family Eulimidae within Hypsogastropoda (Mollusca). Molecular Phylogenetics and Evolution 79: 258-269. DOI:10.1016/j.ympev.2014.06.021
???msg.biblio.abstract.label??? [+] [-]The gastropod family Eulimidae has attracted considerable attention as one of the most diverse groups of parasitic molluscs in terms of number of species and ranges of body plans and parasitic strategies. However, the phylogenetic position of the family has not been established within the Hypsogastropoda and this has hampered the inference of ancestral states in the evolution of the morphology and parasitic strategies. Here we present Bayesian and maximum likelihood phylograms of Hypsogastropoda based on nuclear and mitochondrial loci (18S and 28S rRNA, Histone H3, COI and 16S rRNA) and a better taxonomic sampling than in previous molecular analyses, to determine the position of Eulimidae. The resulting trees suggest Vanikoridae as the sister group of Eulimidae; the two families are collectively placed in the newly redefined superfamily Vanikoroidea, with Truncatelloidea and (potentially paraphyletic) Rissooidea as closest relatives. Vanikorids are protandrous hermaphrodites as are many eulimids and are essentially carnivorous, differing from the mostly gonochoristic and herbivorous/detritivorous Truncatelloidea and Rissooidea. The mode of feeding may have a phylogenetic signal also within Eulimidae, where radula-less species constitute a robust clade. Other new findings include a close affinity of the submarine-cave Pickworthiidae to Cerithioidea and a terminal position of Nystiellidae within the paraphyletic Epitoniidae.
???msg.biblio.biblioSurvey.label??? (1) [+] [-]
???msg.biblio.codeCollection.label??? IE (Échinodermes), IM (Mollusques) -
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) -
Tenorio M.J. & Castelin M. 2016. Genus Profundiconus Kuroda, 1956 (Gastropoda, Conoidea): Morphological and molecular studies, with the description of five new species from the Solomon Islands and New Caledonia. European Journal of Taxonomy 173: 1-45. DOI:10.5852/ejt.2016.173
???msg.biblio.abstract.label??? [+] [-]The genus Profundiconus Kuroda, 1956 is reviewed. The morphological characters of the shell, radular tooth and internal anatomy of species in Profundiconus are discussed. In particular, we studied Profundiconus material collected by dredging in deep water during different scientific campaigns carried out in the Solomon Islands, Madagascar, Papua New Guinea and New Caledonia. We reconstructed a phylogeny of 55 individuals based on partial mitochondrial cox1 gene sequences. The phylogeny shows several clades containing individuals that do not match any of the known species of Profundiconus based on their shell and radular morphologies, and are introduced here as five new species: Profundiconus maribelae sp. nov. from the Solomon Islands; P. virginiae sp. nov. from Chesterfield Plateau (New Caledonia); P. barazeri sp. nov. from Chesterfield Plateau and the Grand Passage area (New Caledonia); P. puillandrei sp. nov. from Norfolk Ridge (New Caledonia), Kermadec Ridge (New Zealand) and possibly Balut Island (Philippines); and P. neocaledonicus sp. nov. from New Caledonia. Furthermore, Profundiconus teramachii forma neotorquatus (da Motta, 1984) is raised to specific status as P. neotorquatus (da Motta, 1984).
???msg.biblio.biblioSurvey.label??? (19) [+] [-]ATIMO VATAE, BATHUS 3, BIOPAPUA, BORDAU 1, CHALCAL 2, CONCALIS, DongSha 2014, EBISCO, EXBODI, MUSORSTOM 6, NORFOLK 1, NORFOLK 2, NanHai 2014, PANGLAO 2005, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 8, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Tenorio M.J., Monnier E. & Puillandre N. 2018. Notes on Afonsoconus Tucker & Tenorio, 2013 (Gastropoda, Conidae), with description of a new species from the Southwestern Indian Ocean. European Journal of Taxonomy(472). DOI:10.5852/ejt.2018.472
???msg.biblio.abstract.label??? [+] [-]Although cone snails are among the most studied group of gastropods, new species are still regularly described. Here, we focus on Afonsoconus Tucker & Tenorio, 2013, a lineage that includes only two species from the Indo-Pacific Ocean. The analysis of molecular (partial mitochondrial cox1 gene sequences) and morphological (shell and radular tooth) characters revealed that the samples collected by dredging in deep water during a recent expedition carried out in the Mozambique Channel are different from the samples collected in the Pacific Ocean. We thus introduce here a new species, Afonsoconus crosnieri sp. nov., from the SW Indian Ocean including records from the Mozambique Channel, the Comoros and Glorieuses Islands, Madagascar, South Africa and Reunion Island.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Tenorio M.J. & Puillandre N. 2023. Revision of the deep-water cone snail fauna from New Caledonia (Gastropoda, Conoidea). European Journal of Taxonomy(896): 1-134. DOI:doi.org/10.5852/ejt.2023.896.2291
???msg.biblio.biblioSurvey.label??? (37) [+] [-]BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, BIOCAL, BIOGEOCAL, CALSUB, CHALCAL 1, CHALCAL 2, CONCALIS, CORAIL 2, EBISCO, EXBODI, HALICAL 1, HALIPRO 1, KANACONO, KANADEEP, LAGON, LITHIST, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, SMIB 10, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, SMIB 9, TERRASSES, VAUBAN 1978-1979, VOLSMAR
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Tu T.H., Dai C.F. & Jeng M.S. 2015. Phylogeny and systematics of deep-sea precious corals (Anthozoa: Octocorallia: Coralliidae). Molecular Phylogenetics and Evolution 84: 173-184. DOI:10.1016/j.ympev.2014.09.031
???msg.biblio.biblioSurvey.label??? (10) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Tu T.H., Dai C.F. & Jeng M.S. 2016. Taxonomic revision of Coralliidae with descriptions of new species from New Caledonia and the Hawaiian Archipelago. Marine Biology Research 12(10): 1003-1038. DOI:10.1080/17451000.2016.1241411
???msg.biblio.abstract.label??? [+] [-]The systematics of Coralliidae has been revised based on molecular phylogenetic analysis and detailed morphological studies. This revision has also revealed the existence of new species. In order to fully accomplish this revision, five new species including Hemicorallium aurantiacum sp. nov., Pleurocorallium bonsaiarborum sp. nov., P. clavatum sp. nov., and P. norfolkicum sp. nov. from New Caledonia, and H. guttatum sp. nov. from the Hawaiian Archipelago are described by integrating the phylogenetic inference and morphological comparisons. Moreover, the type specimens of Corallium tortuosum, H. reginae, H. halmaheirense, P. porcellanum and P. kishinouyei as well as non-type specimens of C. stylasteroides are redescribed. The sclerites of H. reginae, H. halmaheirense, P. porcellanum and C. stylasteroides were first depicted by scanning electron microcopy. A thorough comparison between P. porcellanum and P. kishinouyei indicated that they should be regarded as one species and the former was adopted as the senior synonym. The two new species of Hemicorallium can be separated by morphological features based on the result of multiple factor analysis. A key is proposed for the identification of all existing species of Coralliidae.
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Uribe J.E., Sei M. & Harasewych M.G. 2022. The mitogenome of the sunken wood limpet Notocrater youngi : insights into mitogenome evolution in Lepetellida (Gastropoda: Vetigastropoda). Journal of Molluscan Studies 88(2): eyac009. DOI:10.1093/mollus/eyac009
???msg.biblio.abstract.label??? [+] [-]The complete mitochondrial genome of the pseudococculinid limpet Notocrater youngi was determined using Illumina sequencing and found to be a double-stranded circular molecule 15,915 bp in length. It contains the usual 13 protein-coding genes, 2 ribosomal RNA genes and 22 transfer RNA genes, although with a gene order that differs from those of all other presently known Vetigastropoda, and that is derived within Lepetellida. Phylogenetic analyses based on amino acid sequences join the three pseudococculinid species in a clade and confirm the well-supported clade Scissurelloidea + (Lepetelloidea + Lepetodriloidea) but not a monophyletic Lepetellida as currently understood. Patterns of gene order rearrangements are concordant with these findings.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Vaga C.F., Seiblitz I.G.L., Stolarski J., Capel K.C.C., Quattrini A.M., Cairns S.D., Huang D., Quek R.Z.B. & Kitahara M.V. 2024. 300 million years apart: the extreme case of macromorphological skeletal convergence between deltocyathids and a turbinoliid coral (Anthozoa, Scleractinia), in Collins A. (Ed.), Invertebrate Systematics 38(4). DOI:10.1071/IS23053
???msg.biblio.abstract.label??? [+] [-]The integration of morphological and molecular lines of evidence has enabled the family Deltocyathidae to be erected to accommodate Deltocyathus species that were previously ascribed to the family Caryophylliidae. However, although displaying the same morphological characteristics as other species of Deltocyathus, molecular data suggested that D. magnificus was phylogenetically distant from Deltocyathidae, falling within the family Turbinoliidae instead. To elucidate the enigmatic evolutionary history of this species and skeletal microstructural features, the phylogenetic relationships of Deltocyathidae and Turbinoliidae were investigated using nuclear ultraconserved and exon loci and complete mitochondrial genomes. Both nuclear and mitochondrial phylogenomic reconstructions confirmed the position of D. magnificus within turbinolids. Furthermore, a novel mitochondrial gene order was uncovered for Deltocyathidae species. This gene order was not present in Turbinoliidae or in D. magnificus that both have the scleractinian canonical gene order, further indicating the taxonomic utility of mitochondrial gene order. D. magnificus is therefore formally moved to the family Turbinoliidae and accommodated in a new genus (Dennantotrochus Kitahara, Vaga & Stolarski, gen. nov.). Surprisingly, turbinolids and deltocyathids do not differ in microstructural organisation of the skeleton that consists of densely packed, individualised rapid accretion deposits and thickening deposits composed of fibres perpendicular to the skeleton surface. Therefore, although both families are clearly evolutionarily divergent, macromorphological features indicate a case of skeletal convergence while these may still share conservative biomineralisation mechanisms.
???msg.biblio.biblioSurvey.label??? (6) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
Verheye M.L., Backeljau T. & D'Udekem D'Acoz C. 2017. Locked in the icehouse: Evolution of an endemic Epimeria (Amphipoda, Crustacea) species flock on the Antarctic shelf. Molecular Phylogenetics and Evolution 114: 14-33. DOI:10.1016/j.ympev.2017.05.013
???msg.biblio.biblioSurvey.label??? (10) [+] [-]BATHUS 3, BIOPAPUA, EXBODI, KARUBAR, MAINBAZA, MUSORSTOM 10, MUSORSTOM 8, NORFOLK 2, SALOMON 2, TAIWAN 2000
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Victorero L., Samadi S., O'Hara T.D., Mouchet M., Delavenne J., Leprieur F. & Leroy B. 2023. Global benthic biogeographical regions and macroecological drivers for ophiuroids. Ecography 2023(9): e06627. DOI:10.1111/ecog.06627
???msg.biblio.abstract.label??? [+] [-]Delineating biogeographical regions can provide important insights into the processes shaping large‐scale species distribution patterns. Here we aimed to 1) identify global marine benthic biogeographical regions for ophiuroids extending from shallow waters to the deep sea and 2) quantify the importance of contemporary environmental conditions and geological features in shaping the delineated biogeographical regions. We delineated marine benthic biogeographical regions using a bipartite network analysis applied to a historical dataset of brittle stars. We then examined the faunal exchanges between the regions, and applied random forest models to evaluate the relative role of contemporary environmental conditions and tectonic configuration underlying the proposed biogeographic scheme. We propose ten main large biogeographical regions across the benthos. The biogeographical regions with the highest species richness and endemicity rates were found in the Indo‐Pacific region, Tropical West Atlantic and Southern Ocean, and South America. The key transition regions fall within the subarctic areas of the Pacific and the waters surrounding Southern Australia and New Zealand. Tectonic configuration, surface temperature and salinity were found to be the most important predictors of the ten delineated biogeographical regions. Our biogeographic delineation, including the deep sea, is in partial agreement with those proposed in previous studies. Our results suggest that contemporary environmental conditions (sea water temperature and salinity) strongly influence the modern distribution of ophiuroids, but that plate tectonics left a marked imprint on regional species pools. Future work based on multiple benthic taxa, and with a better understanding of the environmental conditions in the deep sea, are needed to evaluate the robustness of our proposed division.
???msg.biblio.biblioSurvey.label??? (59) [+] [-]ATIMO VATAE, AURORA 2007, AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BERYX 11, BIOCAL, BIOGEOCAL, BIOPAPUA, BOA1, BORDAU 1, BORDAU 2, CHALCAL 1, CHALCAL 2, CORAIL 2, CORINDON 2, DongSha 2014, EBISCO, EXBODI, GUYANE 2014, HALIPRO 1, HALIPRO 2, KANACONO, KANADEEP, KARUBAR, KARUBENTHOS 2, LAGON, LITHIST, MIRIKY, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, PALEO-SURPRISE, PAPUA NIUGINI, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, TAIWAN 2000, TARASOC, VAUBAN 1978-1979, VOLSMAR, Walters Shoal
???msg.biblio.codeCollection.label??? IE (Échinodermes) -
Vilvens C., Williams S.T. & Herbert D.G. 2014. New genus Arxellia with new species of Solariellidae (Gastropoda: Trochoidea) from New Caledonia, Papua New Guinea, Philippines, Western Australia, Vanuatu and Tonga. Zootaxa 3826(1): 255-281. DOI:10.11646/zootaxa.3826.1.8
???msg.biblio.abstract.label??? [+] [-]A new genus, Arxellia, is described in the family Solariellidae. Nine species are referred to this taxon, eight of which are new and are described in this paper (Arxellia trochos n. sp., Arxellia boucheti n. sp., Arxellia herosae n. sp., Arxellia helicoides n. sp., Arxellia tracheia n. sp., Arxellia thaumasta n. sp., Arxellia maestratii n. sp. And Arxellia erythrea n. sp.). The previously described species Bathymophila tenorioi Poppe, Tagaro & Dekker, 2006 is reassigned to Arxellia.
???msg.biblio.biblioSurvey.label??? (17) [+] [-]BATHUS 2, BATHUS 3, BIOCAL, BIOPAPUA, BORDAU 1, BORDAU 2, CHALCAL 2, EXBODI, LITHIST, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, PANGLAO 2005, SMIB 8, VOLSMAR
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Vilvens C. & Williams S.T. 2020. New species of Ilanga (Gastropoda: Trochoidea: Solariellidae) from the Indo-West Pacific. Zootaxa 4732(2): 201-257. DOI:10.11646/zootaxa.4732.2.1
???msg.biblio.abstract.label??? [+] [-]In this study we list and figure a total of 22 species assigned to the genus Ilanga Herbert, 1987 that were collected during recent Paris Museum expeditions, of which 16 are new and described here (listed in the order they appear in the text): Ilanga herberti n. sp., I. euryomphalos n. sp., I. polygramma n. sp., I. stephanophora n. sp., I. harrytaylori n. sp., I. eurystoma n. sp., I. oxeia n. sp., I. cosmia n. sp., I. corrineae n. sp., I. comes n. sp., I. dongshaensis n. sp., I. philia n. sp., I. helicoides n. sp., I. lauensis n. sp., I. mesembrine n. sp. and I. boreia n. sp.. These species occur throughout the Indo-West Pacific, extending the known range of this genus beyond the south west Indian Ocean. We also synonymise Microgaza fulgens Dall, 1907 and Microgaza konos Vilvens, 2009 (syn. nov.) (as I. fulgens). New combinations include Ilanga fulgens and I. navakaensis.
???msg.biblio.biblioSurvey.label??? (42) [+] [-]BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BIOGEOCAL, BIOPAPUA, BOA1, BORDAU 1, BORDAU 2, CONCALIS, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, DongSha 2014, EBISCO, EXBODI, KARUBAR, KAVIENG 2014, LAGON, LIFOU 2000, MAINBAZA, MIRIKY, MUSORSTOM 10, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 1, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2001, TAIWAN 2002, TERRASSES, VAUBAN 1978-1979, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Vilvens C. 2023. New species and new records of Calliostomatidae (Gastropoda: Trochoidea) from western and central Pacific (I): New Caledonia area. Novapex 23(2): 45-76
???msg.biblio.abstract.label??? [+] [-]New records of 21 known Calliostomatidae species from New Caledonia and neighbouring areas are listed, extending the distribution area of some of them. The depth ranges of these species have been completely recalculated based on all the data available for 30 years.
???msg.biblio.biblioSurvey.label??? (15) [+] [-]BATHUS 2, BATHUS 3, BATHUS 4, BIOGEOCAL, CONCALIS, EBISCO, EXBODI, KANACONO, KANADEEP, KANADEEP 2, KOUMAC 2.2, MONTROUZIER, NORFOLK 1, NORFOLK 2, TERRASSES
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Vishnu K., Collot J., Etienne S., Loubrieu B., Patriat M., Tanguy N. & Pertuisot C. 2022. Base de données de sondeurs multifaisceaux et modèles bathymétriques de la Nouvelle-Calédonie – hors lagon
???msg.biblio.biblioSurvey.label??? (9) [+] [-] -
Watling L., Saucier E.H. & France S.C. 2022. Towards a revision of the bamboo corals (Octocorallia): Part 4, delineating the family Keratoisididae. Zootaxa 5093(3): 337-375. DOI:10.11646/zootaxa.5093.3.4
???msg.biblio.abstract.label??? [+] [-]The systematics of bamboo corals of the Family Keratoisididae are evaluated using both DNA sequences and morphological data. Sequence data were obtained from 398 specimens, from which 77 unique haplotypes representing the mtMutS and 18S gene regions were identified. These were aligned with sequences downloaded from GenBank from an additional 12 keratoisids and 6 octocoral outgroups. Phylogenetic analyses recovered seven well-supported major clades, the most recently derived of which consists of several subclades. Each clade and subclade can be characterized by a suite of morphological characters that include axis construction, branching pattern, polyp form, and sclerite type and arrangement. This analysis also shows that keratoisid genera described >100 years ago are paraphyletic and need revision and that a large number of new genera will need to be described.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]
???msg.biblio.codeCollection.label??? IK (Cnidaires) -
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) -
Wicksten M.K. & Guinot D. 2015. Camouflage: carrying behaviour, decoration behaviour, and other modalities of concealment in Brachyura, Treatise on Zoology - Anatomy, Taxonomy, Biology. The Crustacea, Volume 9 Part C (2 vols). Brill:583-638, ISBN:978-90-04-19083-2
???msg.biblio.biblioSurvey.label??? (3) [+] [-]
???msg.biblio.codeCollection.label??? IU (Crustacés) -
Williams S.T., Kano Y., Warén A. & Herbert D.G. 2020. Marrying molecules and morphology: first steps towards a reevaluation of solariellid genera (Gastropoda: Trochoidea) in the light of molecular phylogenetic studies. Journal of Molluscan Studies 86(1): 1-26. DOI:10.1093/mollus/eyz038
???msg.biblio.abstract.label??? [+] [-]The assignment of species to the vetigastropod genus Solariella Wood, 1842, and therefore the family Solariellidae Powell, 1951, is complicated by the fact that the type species (Solariella maculata Wood, 1842) is a fossil described from the Upper Pliocene. Assignment of species to genera has proved difficult in the past, and the type genus has sometimes acted as a ‘wastebasket’ for species that cannot easily be referred to another genus. In the light of a new systematic framework provided by two recent publications presenting the first molecular phylogenetic data for the group, we reassess the shell characters that are most useful for delimiting genera. Shell characters were previously thought to be of limited taxonomic value above the species level, but this is far from the case. Although overall shell shape is not a reliable character, our work shows that shell characters, along with radular and anatomical characters, are useful for assigning species to genera. Sculpture of the early teleoconch (the region immediately following the protoconch) and the columella are particularly useful characters that have not been used regularly in the past to distinguish genera. However, even with the combination of all morphological characters used in this study (shell, radular and eye), a few species are still difficult to assign to genera and in such cases molecular systematic data are essential. In the present study, we discuss 13 genera—12 of which were recovered as well-supported clades in recent molecular systematic studies—and provide morphological characters to distinguish them. We describe several new taxa: Chonospeira n. gen. (referred to as ‘clade B’ in previous molecular systematic studies), Phragmomphalina n. gen. (Bathymophila in part in molecular systematic studies) and Phragmomphalina vilvensi n. sp. (type species of Phragmomphalina n. gen.). We synonymize Hazuregyra Shikama, 1962 with Minolia A. Adams, 1860, Minolia subangulata Kuroda & Habe, 1952 with Minolia punctata A. Adams, 1860 and M. gemmulata Kuroda & Habe, 1971 with M. shimajiriensis (MacNeil, 1960). We also present the following new combinations: Bathymophila bairdii (Dall, 1889), B. dawsoni (Marshall, 1979), B. regalis (Marshall, 1999), B. wanganellica (Marshall, 1999), B. ziczac (Kuroda & Habe in Kuroda, Habe & Oyama, 1971), Chonospeira nuda (Dall, 1896), C. iridescens (Habe, 1961), C. ostreion (Vilvens, 2009), C. strobilos (Vilvens, 2009), Elaphriella corona (Lee & Wu, 2001), E. diplax (Marshall, 1999), E. meridiana (Marshall, 1999), E. olivaceostrigata (Schepman, 1908), E. opalina (Shikama & Hayashi, 1977), Ilanga norfolkensis (Marshall, 1999), I. ptykte (Vilvens, 2009), I. zaccaloides (Vilvens, 2009), Minolia shimajiriensis (MacNeil, 1960), M. watanabei (Shikama, 1962), Phragmomphalina alabida (Marshall, 1979), P. diadema (Marshall, 1999), P. tenuiseptum (Marshall, 1999), Spectamen euteium (Vilvens, 2009), S. basilicum (Marshall, 1999), S. exiguum (Marshall, 1999) and S. flavidum (Marshall, 1999).
???msg.biblio.biblioSurvey.label??? (5) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Williams S.T., Dyal P. & Herbert D.G. 2024. Molecular phylogenetics of the trochid subfamily Umboniinae (Gastropoda: Trochoidea): working towards a new systematic framework. Journal of Molluscan Studies 90(2): eyae008. DOI:10.1093/mollus/eyae008
???msg.biblio.abstract.label??? [+] [-]ABSTRACT We present here the most taxon-rich phylogeny for the trochid subfamily Umboniinae published to date, with representatives from 14 of the 19 known genera, and as a result show that Umboniinae needs comprehensive taxonomic and systematic revision. We identified one clade corresponding to a new genus with four species collected from deeper water than is typical of most umboniine taxa and one new species likely belonging to a second, undescribed genus (all to be described elsewhere). Only four genera, as currently interpreted were recovered, as monophyletic: Umbonium, Lirularia, Monilea and Rossiteria. Zethalia (monotypic for extant taxa), Pseudominolia, Isanda and Parminolia were all represented by a single species (the latter by Gibbula vanwalleghemi; Poppe, Tagaro & Dekker, 2006). Conotalopia, Ethalia, Ethaliella, Ethminolia, Sericominolia and Vanitrochus were all polyphyletic. We formally recognize the following new combinations: Sericominolia glaphyrella (Melvill & Standen, 1895), Sericominolia vitiliginea (Menke, 1843), Vanitrochus ornatus (Sowerby III, 1903) and Parminolia vanwalleghemi (Poppe, Tagaro & Dekker, 2006), although further molecular studies are desirable to confirm these decisions. The first three generic reassignments make Sericominolia and Vanitrochus monophyletic in our tree. We also suggest that Ethaliella cf. rhodomphala (Souverbie, 1875) should be transferred to one of several clades with species previously assigned to Ethminolia, for which an appropriate genus name has not yet been resolved. This decision makes Ethaliella monophyletic. We also identified several cryptic species complexes, including Rossiteria nucleus (Philippi, 1850), the type species of Rossiteria. The phylogeny presented is a first step towards a more resolved systematic framework for Umboniinae and will allow future studies of key morphological innovations.
???msg.biblio.biblioSurvey.label??? (7) [+] [-]
???msg.biblio.codeCollection.label??? IM (Mollusques) -
Williams S.T., Noone E.S., Smith L.M. & Sumner‐Rooney L. 2022. Evolutionary loss of shell pigmentation, pattern, and eye structure in deep‐sea snails in the dysphotic zone. Evolution 76(12): 3026-3040. DOI:10.1111/evo.14647
???msg.biblio.abstract.label??? [+] [-]Adaptations to habitats lacking light, such as the reduction or loss of eyes and pigmentation, have fascinated biologists for centuries, yet have rarely been studied in the deep sea, the earth's oldest and largest light‐limited habitat. Here, we investigate the evolutionary loss of shell pigmentation, pattern, and eye structure across a family of deep‐sea gastropods (Solariellidae). We show that within our phylogenetic framework, loss of these traits evolves without reversal, at different rates (faster for shell traits than eye structure), and over different depth ranges. Using a Bayesian approach, we find support for correlated evolution of trait loss with increasing depth within the dysphotic region. A transition to trait loss occurs for pattern and eye structure at 400–500 m and for pigmentation at 600–700 m. We also show that one of the sighted, shallow‐water species, Ilanga navakaensis, which may represent the “best‐case” scenario for vision for the family, likely has poor spatial acuity and contrast sensitivity. We therefore propose that pigmentation and pattern are not used for intraspecific communication but are important for camouflage from visual predators, and that the low‐resolution vision of solariellids is likely to require high light intensity for basic visual tasks, such as detecting predators.
???msg.biblio.biblioSurvey.label??? (21) [+] [-]BIOPAPUA, BOA1, BORDAU 1, CONCALIS, EBISCO, EXBODI, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, SANTO 2006, TARASOC, TERRASSES, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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 Y., Templado J., Puillandre N. & Zardoya R. 2024. Mitogenomic phylogeny of Nassariidae (Neogastropoda: Buccinoidea). Journal of Molluscan Studies 90(3): eyae020. DOI:10.1093/mollus/eyae020
???msg.biblio.abstract.label??? [+] [-]Mud snails (family Nassariidae) represent a highly diversified lineage within the superfamily Buccinoidea. Recent molecular phylogenies contradicted in some instances the traditional nassariid classification and revealed important levels of homoplasy in phenotypic characters. In order to clarify the boundaries of the family Nassariidae, as well as to inquire on the diversification of the cosmopolitan Nassariinae, a robust phylogenetic framework is needed. Here, the near-complete mitogenomes of 31 species representing almost all lineages of Nassariidae plus several buccinoid outgroups were sequenced. All mitogenomes of buccinoids shared the same gene order, which is identical to the consensus reported for caenogastropods. The monophyly of Nassariidae as previously defined was not confirmed. The reconstructed phylogeny revealed distant relationships between the genera Cyllene, Anentome, Tomlinia, Engoniophos, Phos and Antillophos and the majority of nassariids, represented by Nassariinae + Bullia. Within Nassariinae, a robust phylogeny, which recognized a total of seven regional groups, was reconstructed. The West Atlantic/Mediterranean genus Tritia was divided into three clades. The biogeographical analysis together with the inferred chronogram suggested that Nassariinae might have originated during the late Paleocene in the Indo-Pacific region. Subsequent climate change and continental drift events triggered diversification within the subfamily, leading to the worldwide distribution of current genera.
???msg.biblio.biblioSurvey.label??? (8) [+] [-]ATIMO VATAE, BIOPAPUA, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2012, PAPUA NIUGINI, ZhongSha 2015
???msg.biblio.codeCollection.label??? IM (Mollusques) -
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)
???msg.campaign.menu.documents???
- Devis et factures
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- ???msg.connection.private.label??? (3)
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- Google Earth
- Stations EXBODI, Google Earth
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- ???msg.connection.private.label??? (3)
???msg.campaign.menu.photos???
Collecte : 599 photos
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Organisme : 595 photos
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Substrat : 36 photos
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Débris organiques : 141 photos
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Détritus : 3 photos
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Sur le pont : 10 photos
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???msg.campaign.menu.participants???
???msg.field.stage.byLabel??? :
- Leg 1 (Fri Sep 02 00:00:00 UTC 2011 - Sun Sep 11 00:00:00 UTC 2011) ???msg.table.stage.ship.label??? : Alis
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De gauche à droite : Justine Thubaut, Sarah Samadi, Stéphane Hourdez, Marie-Catherine Boisselier et Laurent Albenga
- Albenga, Laurent ( Muséum national d'Histoire naturelle)
- Collecte - Tri
- Boisselier, Marie-Catherine (Systématique moléculaire, Centre National de la Recherche Scientifique)
- Collecte - Tri
- Hourdez, Stéphane (Biologie évolutive des annélides, Centre National de la Recherche Scientifique)
- Collecte - Tri
- Samadi, Sarah (Biologie évolutive, Institut de Recherche pour le Développement)
- Chef de mission
- Thubaut, Justine (Biologie évolutive, bois coulés, Muséum national d'Histoire naturelle)
- Collecte - Tri
- Leg 2 (Mon Sep 12 00:00:00 UTC 2011 - Thu Sep 29 00:00:00 UTC 2011) ???msg.table.stage.ship.label??? : Alis
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De gauche à droite : Wei-Jen Chen, Eric Pante, Bertrand Richer De Forges, Pierre Lozouet, Laure Corbari et Lee-Ann Galindo
- Chen, Wei-jen (Ichtyologie, National Taiwan Ocean University)
- Collecte - Tri
- Corbari, Laure (Carcinologie, bois coulés, Muséum national d'Histoire naturelle)
- Chef de mission
- Galindo, Lee Ann (Systématique moléculaire, Muséum national d'Histoire naturelle)
- Collecte - Tri
- Lozouet, Pierre (Malacologie, Muséum national d'Histoire naturelle)
- Collecte - Tri
- Pante, Eric (Systématique des Cnidaires, Université de la Rochelle)
- Collecte - Tri
- Richer de Forges, Bertrand (Carcinologie - Benthologie, Muséum national d'Histoire naturelle)
- Collecte - Tri
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| ???msg.field.class.label??? | ???msg.security.label??? | ???msg.table.taxons.count.label??? |
|---|---|---|
| Asteroidea | ???msg.security.public??? | 3 |
| Crinoidea | ???msg.security.public??? | 2 |
