143 stations/gatherings
KARUBENTHOS 2
Référence sismer
http://dx.doi.org/10.17600/15005400Program
General information
Date and place of departure
06/06/2015Date and place of arrival
30/06/2015| Leg | Date of departure | Date of arrival | Departure | Arrival | Ship |
|---|---|---|---|---|---|
| Leg 1 | 07/06/2015 | 16/06/2015 | Antea | ||
| Leg 2 | 21/06/2015 | 29/06/2015 | Antea |
Goals :
Works :
Thanks :
Bibliography (22) [+] [-]
Export the bibliographies
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Baba K. & Wicksten M.K. 2017. Uroptychus nitidus (A. Milne-Edwards, 1880) and related species (Crustacea: Decapoda: Anomura: Chirostylidae) from the western Atlantic. Zootaxa 4221(3): 251-290. DOI:10.11646/zootaxa.4221.3.1
Abstract [+] [-]Eight species of squat lobsters of the genus Uroptychus are reported from the western Atlantic based on the collections of the Museum of Comparative Zoology at Harvard, the Smithsonian Institution and Texas A&M University. Uroptychus nitidus (A. Milne-Edwards, 1880) is reviewed and redescribed, with a syntype taken at Blake Station 200 off Martinique designated as the lectotype. Uroptychus alphonsei n. sp. is named for U. nitidus variety C Chace, 1942, U. fenneri n. sp. for U. nitidus variety A Chace, 1942, and U. janiceae n. sp. for U. nitidus variety B Chace, 1942; U. lindae n. sp. is described on the basis of specimens collected by the Alaminos in the Caribbean Sea off northern Columbia; U. rafai n. sp. is described based on a sole specimen taken from the Straits of Florida; U. reedae n. sp. is described from among the syntypes of U. nitidus; and U. uncifer (A. Milne-Edwards, 1880) is redescribed to elaborate on its specific status, with the designation of lectotype from Blake Station 299 off the coast of Barbados. The number of species of Uroptychus from the western Atlantic now stands at 21. A key to these species is provided.
Accessible surveys cited (1) [+] [-]
Associated collection codes: IU (Crustaceans) -
Chan T.Y., Chakraborty R.D., Purushothaman P., Kuberan G. & Yang C.H. 2018. On Plesionika persica (Kemp, 1925) and P. reflexa Chace, 1985 (Crustacea: Decapoda: Pandalidae) from India. Zootaxa 4382(3): 583-591. DOI:10.11646/zootaxa.4382.3.9
Abstract [+] [-]The availability of Indian specimens of Plesionika persica (Kemp, 1925) and P. reflexa Chace, 1985 provided more information on the taxonomy around these two species. Moreover, it is the first record of P. persica to India. Although P. taiwanica Chan and Yu, 2000 is superficially rather similar to P. persica, there are many differences between them and probably it is inappropriate to establish a species group for these two species. It is likely that all previous records of P. ensis (A. Milne-Edwards, 1881) from India actually represent P. reflexa Chace, 1985. Nevertheless, the present Indian specimens of P. reflexa have more than 10% COI sequence divergence from the topotypic materials of both P. ensis and P. reflexa, and the epipods at the pereiopods III and IV reduced or absent. This data further highlights the confusing taxonomy in the “P. ensis” group.
Accessible surveys cited (2) [+] [-]
Associated collection codes: IU (Crustaceans) -
Chen C.L., Goy J.W., Bracken-grissom H.D., Felder D.L., Tsang L.M. & Chan T.Y. 2016. Phylogeny of Stenopodidea (Crustacea : Decapoda) shrimps inferred from nuclear and mitochondrial genes reveals non-monophyly of the families Spongicolidae and Stenopididae and most of their composite genera. Invertebrate Systematics 30(5): 479-490. DOI:10.1071/IS16024
Abstract [+] [-]The infraorder Stenopodidea is a relatively small group of marine decapod crustaceans including the well known cleaner shrimps, but their higher taxonomy has been rather controversial. This study provides the most comprehensive molecular phylogenetic analyses of Stenopodidea using sequence data from two mitochondrial (16S and 12S rRNA) and two nuclear (histone H3 and sodium–potassium ATPase a-subunit (NaK)) genes. We included all 12 nominal genera from the three stenopodidean families in order to test the proposed evolutionary hypothesis and taxonomic scheme of the group. The inferred phylogeny did not support the familial ranking of Macromaxillocarididae and rejected the reciprocal monophyly of Spongicolidae and Stenopididae. The genera Stenopus, Richardina, Spongiocaris, Odontozona, Spongicola and Spongicoloides are showed to be poly- or paraphyletic, with monophyly of only the latter three genera strongly rejected in the analysis. The present results only strongly support the monophyly of Microprosthema and suggest that Paraspongiola should be synonymised with Spongicola. The three remaining genera, Engystenopus, Juxtastenopus and Globospongicola, may need to be expanded to include species from other genera if their statuses are maintained. All findings suggest that the morphological characters currently adopted to define genera are mostly invalid and substantial taxonomic revisions are required. As the intergeneric relationships were largely unresolved in the present attempt, the hypothesis of evolution of deep-sea sponge-associated taxa from shallow-water free-living species could not be verified here. The present molecular phylogeny, nevertheless, provides some support that stenopoididean shrimps colonised the deep sea in multiple circumstances.
Accessible surveys cited (14) [+] [-]BIOPAPUA, BORDAU 2, EBISCO, GUYANE 2014, KARUBENTHOS 2, KARUBENTHOS 2012, MUSORSTOM 9, NORFOLK 2, Restricted, PALEO-SURPRISE, PAPUA NIUGINI, SALOMON 2, SANTO 2006, Restricted
Associated collection codes: IU (Crustaceans) -
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
Abstract [+] [-]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.
Accessible surveys cited (13) [+] [-]ATIMO VATAE, CEAMARC-AA, CONCALIS, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, TARASOC
Associated collection codes: IM (Molluscs) -
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
Abstract [+] [-]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.
Accessible surveys cited (13) [+] [-]ATIMO VATAE, CEAMARC-AA, CONCALIS, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMON 2, TARASOC
Associated collection codes: IM (Molluscs) -
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
Abstract [+] [-]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.
Accessible surveys cited (20) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MAINBAZA, MIRIKY, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, TARASOC, Tuhaa Pae 2013
Associated collection codes: IM (Molluscs) -
Garrigues B. & Lamy D. 2016. Description de trois nouvelles espèces de Muricidae (Mollusca, Gastropoda) collectées durant l’expédition du MNHN en Guyane Française et réhabilitation de Murex mexicanus Petit de la Saussaye, 1852. Xenophora Taxonomy 12: 30-44
Abstract [+] [-]Trois nouvelles espèces de Muricidae ont été collectées au cours de l’expédition « La Planète Revisitée » en Guyane Française en 2014-2015. Les deux premières, Phyllonotus guyanensis n. sp. et Phyllonotus salutensis n. sp. appartiennent au genre Phyllonotus Swainson, 1833. Dans la région Atlantique Ouest, cinq espèces sont actuellement répertoriées dans ce genre : Phyllonotus pomum (Gmelin, 1791), P. oculatus (Reeve, 1845), P. margaritensis (Abbott, 1958), P. globosus Emmons, 1858 et P. whymani Petuch & Sargent, 2011. Phyllonotus guyanensis n. sp. décrit ici est comparé à deux espèces proches : P. pomum et P. whymani. Phyllonotus pomum est largement répandu de la Caroline du Nord au Nord de l’Amérique du Sud tandis que P. whymani n’est connu que de sa localité-type, Dry Tortuga, Florida Keys. La deuxième espèce, Phyllonotus salutensis n. sp., est comparée à P. margaritensis des Iles du nord-est du Venezuela, P. globosus de la presqu’île du Paraguana au nord-ouest du Venezuela et P. pomum. Murex mexicanus Petit de la Saussaye, 1852, du Golfe du Mexique, (non Murex mexicanus Stearns, 1894 = Chicoreus maurus (Broderip, 1833)) a toujours été confondu avec P. pomum. Il est ici réhabilité sous le taxon de Phyllonotus mexicanus (Petit de la Saussaye, 1852). Phyllonotus oculatus se distingue de toutes les autres espèces nommées ci-dessus par une protoconque multispirale (Houart, 1987) et n’est pas abordé ici. La troisième espèce est une Favartia Jousseaume, 1880, Favartia charlesi n. sp. Elle est comparée avec l’espèce voisine F. hidalgoi (Crosse, 1869) rencontrée du Golfe du Mexique au Sud du Brésil entre 120 et 400 m de profondeur.
Accessible surveys cited (4) [+] [-]
Associated collection codes: IM (Molluscs) -
Garrigues B. & Lamy D. 2017. Description d’une nouvelle espèce de Dermomurex (Muricidae, Muricinae) collectée au cours de l’expédition KARUBENTHOS 2 en Guadeloupe, Antilles Françaises. Xenophora Taxonomy 16: 39-43
Abstract [+] [-]Dermomurex spinosus, nouvelle espèce de Guadeloupe, Antilles Françaises, est décrit dans ce travail. Il a été récolté en juin 2015 au cours de la campagne KARUBENTHOS 2 du Muséum d’Histoire Naturelle de Paris (MNHN) par 312-480 m de profondeur. Sept espèces appartenant au genre Dermomurex sont répertoriées en Guadeloupe: Dermomurex abyssicola (Crosse, 1865), D. boucheti Garrigues & Merle, 2014, D. pruvosti Garrigues & Merle, 2014, D. fajouensis Garrigues & Merle, 2014, D. tararensis Garrigues & Merle, 2014, D. alabastrum (Adams, 1864) et D. worsfoldi Vokes, 1992. Le séquençage a permis de rapprocher avec un bon support statistique la nouvelle espèce de D. boucheti et de D. neglecta (Habe & Kosuge, 1971) publié par Marco et al. en 2010 (N. Puillandre communication personnelle). Dermomurex spinosus n. sp. est comparé à ces deux espèces ainsi qu’à deux autres espèces proches : Dermomurex (Takia) gofasi Houart, 1996 et D. (T.) infrons Vokes, 1974.
Accessible surveys cited (3) [+] [-]
Associated collection codes: IM (Molluscs) -
Garrigues B. & Lamy D. 2018. Muricidae récoltés au cours de la campagne KARUBENTHOS 2 du MNHN dans les eaux profondes de Guadeloupe (Antilles Françaises) et description de trois nouvelles espèces des genres Pagodula et Pygmaepterys (Mollusca, Gastropoda). Xenophora Taxonomy(20): 34-52
Abstract [+] [-]Cet article comprend deux parties. La première est une liste des muricidés récoltés au cours de la campagne KARUBENTHOS 2 (2015) dans les eaux profondes des îles de Guadeloupe. Les Coralliophilinae sont exclus de cette étude et seront traités ultérieurement. Hormis les Coralliophilinae, 28 espèces ont été recensées pour le moment. Parmi elles, quatre étaient nouvelles pour la science. Le Dermomurex spinosus Garrigues & Lamy, 2017 a été récemment décrit. Les trois autres appartenant aux genres Pagodula et Pygmaepterys font l’objet de la deuxième partie.
Accessible surveys cited (2) [+] [-]
Associated collection codes: IM (Molluscs) -
Glover E.A. & Taylor J.D. 2016. Pleurolucina from the western Atlantic and eastern Pacific Oceans: a new intertidal species from Curaçao with unusual shell microstructure (Mollusca, Bivalvia, Lucinidae). ZooKeys 620: 1-19. DOI:10.3897/zookeys.620.9569
Abstract [+] [-]A new shallow water species of the lucinid bivalve Pleurolucina is described from Curaçao in the southern Caribbean Sea and compared with known species of the genus from the western Atlantic and eastern Pacific Oceans. Although confused with the Floridian species P. leucocyma, it is most similar to the eastern Pacific P. undata. As in all studied lucinids, the new species possesses symbiotic bacteria housed in the ctenidia. The shell microstructure is unusual with repeated and intercalated conchiolin layers that have sublayers of ‘tulip-shaped’ calcareous spherules. Predatory drillings by naticid gastropods frequently terminate at the conchiolin layers.
Accessible surveys cited (3) [+] [-]
Associated collection codes: IM (Molluscs) -
Phuong M.A., Alfaro M.E., Mahardika G.N., Marwoto R.M., Prabowo R.E., Von rintelen T., Vogt P.W., Hendricks J.R. & Puillandre N. 2018. Lack of signal for the impact of venom gene diversity on speciation rates in cone snails. bioRxiv 359976. DOI:10.1101/359976
Abstract [+] [-]Understanding why some groups of organisms are more diverse than others is a central goal in macroevolution. Evolvability, or lineages' intrinsic capacity 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 venom 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, 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 whether or not we detected a signal depended on the dataset and the method. If our results remain true with increased sampling in future studies, they suggest that the rapid evolution of Conidae venom may cause other factors to become more critical to diversification, such as ecological opportunity or traits that promote isolation among lineages.
Accessible surveys cited (25) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, CONCALIS, EBISCO, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, KAVIENG 2014, MADEEP, MAINBAZA, MIRIKY, NORFOLK 2, NanHai 2014, Restricted, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, SALOMONBOA 3, SANTO 2006, TAIWAN 2013, TERRASSES, Restricted
Associated collection codes: IM (Molluscs) -
Pinheiro M. & Boos H. 2016. Livro Vermelho dos Crustáceos do Brasil: Avaliação 2010-2014. Sociedade Brasileira de Carcinologia, Porto Alegre, 466 pp. ISBN:978-85-930030-0-4
Accessible surveys cited (1) [+] [-]
Associated collection codes: IU (Crustaceans) -
Poore G.C.B. 2018. Caribbean species of Eiconaxius (Decapoda: Axiidea: Axiidae). Zootaxa 4524(1): 139. DOI:10.11646/zootaxa.4524.1.11
Abstract [+] [-]The type status of specimens of three species of the axiid genus Eiconaxius Bate, 1888 from the Caribbean Sea is clarified. Eiconaxius agassizi Bouvier, 1905, E. borradailei Bouvier, 1905 and E. caribbaeus (Faxon, 1896) are diagnosed and illustrated. Axius (Eiconaxius) communis Bouvier, 1905, Axius (Eiconaxius) rotundifrons Bouvier, 1905, and Axius (Eiconaxius) caribbaeus carinatus Bouvier, 1925, hitherto treated as valid species, are synonymised with E. caribbaeus. Lectotypes are selected for Eiconaxius agassizi Bouvier, 1905 and Eiconaxius borradailei Bouvier, 1905.
Accessible surveys cited (1) [+] [-]
Associated collection codes: IU (Crustaceans) -
Poore G.C.B. & Dworschak P.C. 2018. The Eiconaxius cristagalli species complex (Decapoda, Axiidea, Axiidae). Memoirs of Museum Victoria 77: 105-120. DOI:10.24199/j.mmv.2018.77.06
Abstract [+] [-]Four species of Eiconaxius are known to possess a denticulate median rostral carina: E. antillensis Bouvier, 1905, E. asper Rathbun, 1906, E. cristagalli Faxon, 1893, and E. indicus (De Man, 1907). They are reviewed and two similar new species are described: E. dongshaensis sp. nov., and E. gololobovi sp. nov. A key to distinguish them is presented.
Accessible surveys cited (6) [+] [-]
Associated collection codes: IU (Crustaceans) -
Poupin J. & Corbari L. 2016. A preliminary assessment of the deep-sea Decapoda collected during the KARUBENTHOS 2015 Expedition to Guadeloupe Island. Zootaxa 4190(1): 1-107. DOI:10.11646/zootaxa.4190.1.1
Abstract [+] [-]A preliminary assessment of the deep-sea Decapoda is proposed for Guadeloupe Island based solely on high definition macro photographs taken during the KARUBENTHOS 2015 Expedition to the Island (R/V Antea, 7–29 June 2015). Overall, 190 species are recognized, several of which are depicted with their fresh color for the first time. Previous records in the Lesser Antilles are documented and the geographic distribution of the species in these Islands is given. The historical contribution of the steamer Blake (1878–1879) in the Lesser Antilles is emphasized. All species inventoried during KARUBENTHOS 2015 were already reported in the western Atlantic but 34 of them are new records for the Lesser Antilles and 116 are reported for the first time from Guadeloupe Island. This preliminary inventory is estimated to include about 38% of the deep-sea Decapoda potentially occurring around Guadeloupe Island.
Accessible surveys cited (2) [+] [-]
Associated collection codes: IU (Crustaceans) -
Rodriguez-flores P.C., Macpherson E. & Machordom A. 2018. Three new species of squat lobsters of the genus Munidopsis Whiteaves, 1874, from Guadeloupe Island, Caribbean Sea (Crustacea, Decapoda, Munidopsidae). Zootaxa 4422(4): 569. DOI:10.11646/zootaxa.4422.4.7
Abstract [+] [-]The genus Munidopsis is one of the most diverse genera within squat lobsters. Here, three new species of Munidopsis, M. cornuata n. sp., M. senticosa n. sp., and M. turgida n. sp., from <500 m off Guadeloupe Island (Caribbean Sea), are fully described and illustrated. Among the Atlantic species of the genus, M. cornuata n. sp. belongs to the group of species having the dorsal surface of the carapace with spines and is most similar to M. robusta (A. Milne-Edwards, 1880), from the Gulf of Mexico and Caribbean Sea. Munidopsis senticosa n. sp. resembles M. barbarae (Boone, 1927) from the Bahamas and the Gulf of Mexico and M. penescabra Pequegnat & Williams 1995, from off Georgia and Gulf of Mexico; the three species belong to the group having the carapace covered with sharp spines. Finally, M. turgida n. sp. is characterized by having the dorsal surface of the carapace, abdomen and pereiopods covered by granules; and resembles M. granulens Mayo, 1972, from NW Caribbean Sea. Apart from the morphological evidence, the analysis of mitochondrial genes (COI and 16S) supports establishing these new species, showing very high genetic divergences compared to their congeners (from 14.5 to 17% for COI, and 7.7 to 12.8% for 16S data).
Accessible surveys cited (1) [+] [-] -
Rodríguez-flores P.C., Macpherson E. & Machordom A. 2019. Revision of the squat lobsters of the genus Leiogalathea Baba, 1969 (Crustacea, Decapoda, Munidopsidae) with the description of 15 new species. Zootaxa 4560(2): 201-256. DOI:10.11646/zootaxa.4560.2.1
Abstract [+] [-]The genus Leiogalathea Baba, 1969 currently contains only two benthic species both occurring on the continental shelves and slope: L. laevirostris (Balss, 1913), widely reported in the Indo-Pacific region, and L. agassizii (A. Milne Edwards, 1880), from both sides of the Central Atlantic. A certain degree of morphological variability linked to their geographic distributions was previously noticed, mostly in L. laevirostris. In the present study, we revise numerous specimens collected from the Atlantic, Indian and Pacific Oceans, analysing morphological and molecular characters (COI and 16S rRNA). We found 15 new species; all of them are distinguished from L. laevirostris and L. agassizii by subtle but constant morphological differences and show clear genetic separation. Furthermore, L. imperialis (Miyake & Baba, 1967), previously synonymized with L. laevirostris, was found to be a valid species. All species are described and illustrated. Species of the genus Leiogalathea are morphologically distinguishable on the basis of the spinulation of the carapace, the shape and the armature of the rostrum, the shape of the propodi of the walking legs, and the pattern of the setae covering on rostrum, carapace and chelae. Some species are barely discernible on the basis of these characters but are highly divergent genetically.
Accessible surveys cited (29) [+] [-]BATHUS 3, BERYX 11, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 2, CHALCAL 2, EBISCO, HALIPRO 2, KANACONO, KANADEEP, KARUBAR, KARUBENTHOS 2, KAVIENG 2014, MADEEP, MUSORSTOM 4, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PAPUA NIUGINI, SALOMON 1, SANTO 2006, SMIB 3, SMIB 4, TARASOC, VOLSMAR
Associated collection codes: IU (Crustaceans) -
Rubio F. & Rolán E. 2018. New species of Lyocyclidae Thiele, 1925 (Gastropoda: Caenogastropoda) from the Caribbean. Novapex 19(4): 95-105
Abstract [+] [-]Four new species of the genus Lyocyclus are described from deep waters of the Caribbean. All these species are compared with Lyocyclus pernambucensis (Watson, 1886) the only previously known species living in the South Atlantic.
Accessible surveys cited (2) [+] [-]
Associated collection codes: IM (Molluscs) -
Strong E.E., Puillandre N., Beu A.G., Castelin M. & Bouchet P. 2019. Frogs and tuns and tritons – A molecular phylogeny and revised family classification of the predatory gastropod superfamily Tonnoidea (Caenogastropoda). Molecular Phylogenetics and Evolution 130: 18-34. DOI:10.1016/j.ympev.2018.09.016
Abstract [+] [-]The Tonnoidea is a moderately diverse group of large, predatory gastropods with ∼360 valid species. Known for their ability to secrete sulfuric acid, they use it to prey on a diversity of invertebrates, primarily echinoderms. Tonnoideans currently are classified in seven accepted families: the comparatively well known, shallow water Bursidae, Cassidae, Personidae, Ranellidae, and Tonnidae, and the lesser-known, deep water Laubierinidae and Pisanianuridae. We assembled a mitochondrial and nuclear gene (COI, 16S, 12S, 28S) dataset for ∼80 species and 38 genera currently recognized as valid. Bayesian analysis of the concatenated dataset recovered a monophyletic Tonnoidea, with Ficus as its sister group. Unexpectedly, Thalassocyon, currently classified in the Ficidae, was nested within the ingroup as the sister group to Distorsionella. Among currently recognized families, Tonnidae, Cassidae, Bursidae and Personidae were supported as monophyletic but the Ranellidae and Ranellinae were not, with Cymatiinae, Ranella and Charonia supported as three unrelated clades. The Laubierinidae and Pisanianuridae together form a monophyletic group. Although not all currently accepted genera have been included in the analysis, the new phylogeny is sufficiently robust and stable to the inclusion/exclusion of nonconserved regions to establish a revised family-level classification with nine families: Bursidae, Cassidae, Charoniidae, Cymatiidae, Laubierinidae, Personidae, Ranellidae, Thalassocyonidae and Tonnidae. The results reveal that many genera as presently circumscribed are para- or polyphyletic and, in some cases support the rescue of several genus-group names from synonymy (Austrosassia, Austrotriton, Laminilabrum, Lampadopsis, Personella, Proxicharonia, Tritonoranella) or conversely, support their synonymization (Biplex with Gyrineum). Several species complexes are also revealed that merit further investigation (e.g., Personidae: Distorsio decipiens, D. reticularis; Bursidae: Bursa tuberosissima; Cassidae: Echinophoria wyvillei, Galeodea bituminata, and Semicassis bisulcata). Consequently, despite their teleplanic larvae, the apparently circumglobal distribution of some tonnoidean species is the result of excessive synonymy. The superfamily is estimated to have diverged during the early Jurassic (∼186 Ma), with most families originating during a narrow ∼20 My window in Albian-Aptian times as part of the Mesozoic Marine Revolution.
Accessible surveys cited (20) [+] [-]ATIMO VATAE, AURORA 2007, CONCALIS, EBISCO, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, MAINBAZA, MIRIKY, NORFOLK 2, Restricted, PANGLAO 2004, PANGLAO 2005, SALOMON 2, SANTO 2006, TAIWAN 2004, TERRASSES, Restricted, ZhongSha 2015
Associated collection codes: IM (Molluscs) -
Taylor J.D. & Glover E.A. 2016. Lucinid bivalves of Guadeloupe: diversity and systematics in the context of the tropical Western Atlantic (Mollusca: Bivalvia: Lucinidae). Zootaxa 4196(3): 301-380. DOI:10.11646/zootaxa.4196.3.1
Abstract [+] [-]Intensive sampling of molluscs from the intertidal to depths of 800 m around the islands of Guadeloupe in the Lesser Antilles (KARUBENTHOS 2012, 2015) recovered 25 species of Lucinidae. All the Guadeloupe species are described and illustrated including details of larval shells and the taxonomy revised within the context of the wider western Atlantic fauna and recent classifications. Concurrent molecular analysis has helped separate frequently confounded species. ‘Myrtea’ pristiphora is placed in the Leucosphaerine genus Myrtina previously known from the Indo-West Pacific. A second western Atlantic species of Callucina, C. pauperatus previously known from the Pliocene of Jamaica is recognised from the southern Caribbean and off Brazil. The deeper water species ‘Myrteopis’ lens is placed in Afrolucina previously known from the eastern Atlantic. Lucinids commonly identified as Ctena orbiculata are shown to belong to two distinct species, C. orbiculata in the Gulf of Mexico and Florida and C. imbricatula in the Caribbean. Epicodakia is recognised for the first time in the western Atlantic with E. pectinata widely distributed across the region and E. filiata recorded from deeper water. Three species of Lucina are recognised, Lucina pensylvanica in the Gulf of Mexico and Florida and the similar Lucina roquesana from the Caribbean and Bahamas while the smaller L. aurantia has a wide distribution from central America to the Bahamas. A new species of Parvilucina, P. latens is described; this is similar to P. pectinella but has an internal ligament. The long problematic species ‘Codakia’ cubana is assigned to Ferrocina. A new genus, Guyanella is introduced for Parvilucina clenchi the smallest known lucinid. A critical reassessment of the lucinid fauna of the western Atlantic Ocean identifies 46 species for the region with 33 of these living at depths less than 200 m. Deeper-water habitats have been much less investigated except at sites of hydrocarbon seeps. Some species are widespread throught the whole region but others have more restricted ranges. Notable are species pairs, for example of Ctena, Lucina, Lucinisca and Parvilucina that are either largely Caribbean or Gulf of Mexico/Floridian in distribution. Although extralimital, two problematic species from the mid-south Atlantic island of St Helena are refigured and placed in Cavilinga.
Accessible surveys cited (4) [+] [-]
Associated collection codes: IM (Molluscs) -
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
Abstract [+] [-]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.
Accessible surveys cited (10) [+] [-]ATIMO VATAE, BIOPAPUA, EXBODI, GUYANE 2014, INHACA 2011, KARUBENTHOS 2, KARUBENTHOS 2012, MADEEP, PANGLAO 2004, PAPUA NIUGINI
Associated collection codes: IM (Molluscs) -
Tongboonkua P., Lee M.Y. & Chen W.J. 2018. A new species of sinistral flatfish of the genus Chascanopsetta (Teleostei: Bothidae) from off Papua New Guinea, western Pacific Ocean. Zootaxa 4476(1): 168. DOI:10.11646/zootaxa.4476.1.16
Abstract [+] [-]Left-eyed flounders of the genus Chascanopsetta Alcock 1894 (Bothidae) occur in the Indian, Pacific, and Atlantic oceans at depths ranging from 120 to 1500 meters. They possess some unique features in bothid fishes including a strongly compressed and elongated body and a tremendously large mouth. Currently, nine species of Chascanopsetta are recognized, and three of them (C. micrognatha Amaoka & Yamamoto 1984, C. lugubris Alcock 1894 and C. prognatha Norman 1939) are distributed in the West Pacific. We collected 25 specimens of Chascanopsetta during 11 biodiversity expeditions carried out mainly in the West Pacific. Among them, eight specimens taken off Papua New Guinea present morphological features that differ from those of the three nominal species known in the West Pacific. In this study, we examined these eight specimens of unknown affinity and compared their morphology to that of specimens of other congeneric species. Results of these comparisons showed that these specimens represent an undescribed species of Chascanopsetta, named herein, C. novaeguineae sp. nov.. The new species resembles C. elski Foroshchuk 1991, which is known only from the Saya de Malha Bank in the western Indian Ocean, in having a high number of gill rakers (> 13). However, the combination of the following characters further distinguishes C. novaeguineae sp. nov. from C. elski: longer jaws, narrower interorbital width, and number of pseudobranches (21–25 vs. 26–27). The DNA sequences from the mitochondrial cytochrome oxidase subunit I (COI) gene from C. novaeguineae sp. nov. and other species were obtained and compared to confirm its taxonomic status and to infer its tentative phylogenetic position within the Chascanopsetta.
Accessible surveys cited (11) [+] [-]AURORA 2007, BIOPAPUA, DongSha 2014, KANACONO, KANADEEP, KARUBENTHOS 2, KAVIENG 2014, MADEEP, NanHai 2014, SALOMONBOA 3, ZhongSha 2015
Associated collection codes: IC (Ichthyology)
List of photos
Collecte : 488 photos
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Contexte : 11 photos
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Organisme : 160 photos
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Organisme sur débris organiques : 12 photos
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Substrat : 1 photo
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Débris organiques : 15 photos
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Sur le pont : 99 photos
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Stations map
GoogleEarth file (.kml)
List of stations
Taxonomy by access
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