KOUMAC 2.1
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Bibliographie (11) [+] [-]
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Chow L.H., De grave S., Anker A., Poon K.K.Y., Ma K.Y., Chu K.H., Chan T. & Tsang L.M. 2021. Distinct suites of pre‐ and post‐adaptations indicate independent evolutionary pathways of snapping claws in the shrimp family Alpheidae (Decapoda: Caridea). Evolution 75(11): 2898-2910. DOI:10.1111/evo.14351
Campagnes accessibles citées (4) [+] [-]
Codes des collections associés: IU (Crustacés) -
Fassio G., Stefani M., Russini V., Buge B., Bouchet P., Treneman N., Malaquias M.A.E., Schiaparelli S., Modica M.V. & Oliverio M. 2022. Neither slugs nor snails: a molecular reappraisal of the gastropod family Velutinidae. Zoological Journal of the Linnean Society: 1-41. DOI:10.1093/zoolinnean/zlac091
Résumé [+] [-]Abstract The systematics of the marine mollusc family Velutinidae has long been neglected by taxonomists, mainly because their often internal and fragile shells offer no morphological characters. Velutinids are usually undersampled owing to their cryptic mantle coloration on the solitary, social or colonial ascidians on which they feed and lay eggs. In this study, we address the worldwide diversity and phylogeny of Velutinidae based on the largest molecular dataset (313 specimens) to date, accounting for > 50% of the currently accepted genera, coupled with morphological and ecological data. Velutinids emerge as a diverse group, encompassing four independent subfamily-level lineages, two of which are newly described herein: Marseniopsinae subfam. nov. and Hainotinae subfam. nov. High diversity was found at genus and species levels, with two newly described genera (Variolipallium gen. nov. and Pacifica gen. nov.) and ≥ 86 species in the assayed dataset, 58 of which are new to science (67%). Velutinidae show a remarkable morphological plasticity in shell morphology, mantle extension and chromatic patterns. This variability is likely to be the result of different selective forces, including habitat, depth and trophic interactions.
Campagnes accessibles citées (23) [+] [-]ATIMO VATAE, BIOMAGLO, BIOPAPUA, CEAMARC-AA, CORSICABENTHOS 1, CORSICABENTHOS 2, CORSICABENTHOS 3, GUYANE 2014, ILES DU SALUT, KANACONO, KANADEEP 2, KARUBENTHOS 2, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, MADEEP, MADIBENTHOS, PANGLAO 2004, PAPUA NIUGINI, SAKIZAYA 2019, SANTO 2006, Tuhaa Pae 2013, ZhongSha 2015
Codes des collections associés: IM (Mollusques) -
Fassio G., Bouchet P., Oliverio M. & Strong E.E. 2022. Re-evaluating the case for poecilogony in the gastropod Planaxis sulcatus (Cerithioidea, Planaxidae). BMC Ecology and Evolution 22(1): 13. DOI:10.1186/s12862-022-01961-7
Résumé [+] [-]Background: Planaxis sulcatus has been touted as a textbook example of poecilogony, with members of this wideranging Indo-Pacific marine gastropod said to produce free-swimming veligers as well as brooded juveniles. A recent paper by Wiggering et al. (BMC Evol Biol 20:76, 2020) assessed a mitochondrial gene phylogeny based on partial COI and 16S rRNA sequences for 31 individuals supplemented by observations from the brood pouch of 64 mostly unsequenced individuals. ABGD and bGYMC supported three reciprocally monophyletic clades, with two distributed in the Indo-Pacific, and one restricted to the northern Indian Ocean and Red Sea. Given an apparent lack of correlation between clade membership and morphological differentiation or mode of development, the reported 3.08% maximum K2P model-corrected genetic divergence in COI among all specimens was concluded to represent population structuring. Hence, the hypothesis that phylogenetic structure is evidence of cryptic species was rejected and P. sulcatus was concluded to represent a case of geographic poecilogony. Results: Our goal was to reassess the case for poecilogony in Planaxis sulcatus with a larger molecular dataset and expanded geographic coverage. We sequenced an additional 55 individuals and included published and unpublished sequence data from other sources, including from Wiggering et al. Our dataset comprised 108 individuals (88 COI, 81 16S rRNA) and included nine countries unrepresented in the previous study. The expanded molecular dataset yielded a maximum K2P model-corrected genetic divergence among all sequenced specimens of 12.09%. The value of 3.08% erroneously reported by Wiggering et al. is the prior maximal distance value that yields a single-species partition in ABGD, and not the maximum K2P intraspecific divergence that can be calculated for the dataset. The bGMYC analysis recognized between two and six subdivisions, while the best-scoring ASAP partitions recognized two, four, or five subdivisions, not all of which were robustly supported in Bayesian and maximum likelihood phylogenetic analyses of the concatenated and single gene datasets. These hypotheses yielded maximum intra-clade genetic distances in COI of 2.56–6.19%, which are more consistent with hypothesized species-level thresholds for marine caenogastropods. Conclusions: Based on our analyses of a more comprehensive dataset, we conclude that the evidence marshalled by Wiggering et al. in support of Planaxis sulcatus comprising a single widespread, highly variable species with geographic poecilogony is unconvincing and requires further investigation in an integrative taxonomic framework.
Campagnes accessibles citées (5) [+] [-]
Codes des collections associés: IM (Mollusques) -
Fedosov A.E. & Puillandre N. 2020. Integrative taxonomy of the Clavus canalicularis species complex (Drilliidae, Conoidea, Gastropoda) with description of four new species. Molluscan Research 40(3): 251-266. DOI:10.1080/13235818.2020.1788695
Résumé [+] [-]The conoidean family Drilliidae Olsson, 1964 is a species-rich lineage of marine gastropods, showing a high degree of diversification in comparison to other families of Conoidea. Despite intensive molecular phylogenetic studies during the last decade that have led to notable rearrangements of conoidean systematics, the genus- and species-level taxonomy of Drilliidae has not thus far been affected and remains entirely based on shell features. In the current study we revisit species delimitation in a morphological cluster of species from the Indo-Pacific referred to as the Clavus canalicularis complex, using an integrative taxonomy approach. The species in the complex possess robust thick-walled shells typically over 15 mm in height with sculpture of prominent rounded nodules located at the whorl’s shoulder, sometimes sharp and squamiform, or producing long spines. We find that in addition to five known species, the complex comprises four new species. These are described as Clavus brianmayi n. sp. (New Caledonia), Clavus davidgilmouri n. sp. (the Philippines), Clavus andreolbrichi n. sp. (Vanuatu and New Ireland) and Clavus kirkhammetti n. sp. (Madagascar). Clavus exasperatus (Reeve, 1843), which was previously considered widely distributed in IndoPacific, is shown to be confined to the western Indian Ocean.
Campagnes accessibles citées (5) [+] [-]
Codes des collections associés: IM (Mollusques) -
Feliciano K., Malaquias M.A.E., Stout C., Brenzinger B., Gosliner T.M. & Valdés Á. 2021. Molecular and morphological analyses reveal pseudocryptic diversity in Micromelo undatus (Bruguière, 1792) (Gastropoda: Heterobranchia: Aplustridae). Systematics and Biodiversity: 1-25. DOI:10.1080/14772000.2021.1939458
Campagnes accessibles citées (5) [+] [-]
Codes des collections associés: IM (Mollusques) -
Ghanimi H., Schrödl M., Goddard J.H.R., Ballesteros M., Gosliner T.M., Buske Y. & Valdés Á. 2020. Stargazing under the sea: molecular and morphological data reveal a constellation of species in the Berthella stellata (Risso, 1826) species complex (Mollusca, Heterobranchia, Pleurobranchidae). Marine Biodiversity 50(1): 11. DOI:10.1007/s12526-019-01027-w
Résumé [+] [-]Molecular and morphological evidence support the view that the widely distributed species Berthella stellata (Risso, 1826) is a species complex of at least eight different species. The closely related species Berthella plumula (Montagu, 1803), examined for comparison, is also a complex of two species; the name B. plumula is retained for the Atlantic species and the name Berthella perforata (Philippi, 1844) is proposed for the Mediterranean species. The B. stellata species complex forms a monophyletic group when the Eastern Pacific species Berthella strongi (MacFarland, 1966) is included. Based on a critical review of the literature, the name Berthella stellata is retained for the Eastern Atlantic and Mediterranean species, and the name Berthella pellucida (Pease, 1860) is resurrected for a species found in the Hawaiian Islands. Two new species from the Caribbean region (Berthella nebula sp. nov., Berthella vialactea sp. nov.) and one from the Eastern Pacific (Berthella andromeda sp. nov.) are described herein, but the status of the Brazilian species B. tupala Er. Marcus, 1957 remains uncertain. Two possible new species from the Eastern Pacific, represented by one specimen each, were recovered in the phylogenetic analyses but not formally described. It is hypothesized that additional species of this complex may occur in other parts of the Indo-Pacific tropics, particularly in the Indian Ocean.
Campagnes accessibles citées (1) [+] [-]
Codes des collections associés: IM (Mollusques) -
Goto R., Takano T., Eernisse D.J., Kato M. & Kano Y. 2021. Snails riding mantis shrimps: Ectoparasites evolved from ancestors living as commensals on the host’s burrow wall. Molecular Phylogenetics and Evolution 163: 107122. DOI:10.1016/j.ympev.2021.107122
Résumé [+] [-]The molluscan class Gastropoda includes over 5,000 parasitic species whose evolutionary origins remain poorly understood. Marine snails of the genus Caledoniella (Caledoniellidae) are obligate parasites that live on the abdominal surface of the gonodactylid mantis shrimps. They have highly modified morphological characteristics specialized to the ectoparasitic lifestyle that make it difficult to infer their close relatives, thereby posing a question about their current systematic position in the superfamily Vanikoroidea. In the present study, we performed molecular phylogenetic analyses using three nuclear and three mitochondrial gene sequences to unveil the phylogenetic position of these enigmatic snails. The resulting trees recovered Caledoniella in the su perfamily Truncatelloidea and within a subclade of commensal species that live on the burrow wall of marine benthic invertebrates. More specifically, Caledoniella formed the sister clade to a commensal snail species living in mantis-shrimp burrows and they collectively were sister to Sigaretornus planus (formerly in the family Tornidae or Vitrinellidae), a commensal living in echiuran burrows. This topology suggests that the species of Caledoniella achieved their ectoparasitic mode of life through the following evolutionary pathway: (1) invasion into the burrows of benthic invertebrates, (2) specialization to mantis shrimps, and (3) colonization of the host body surface from the host burrow wall with the evolution of the parasitic nature. The final step is likely to have been accompanied by the acquisition of a sucker on the metapodium, the loss of the radula and operculum, and the formation of monogamous pair bonds. The present molecular phylogeny also suggested parallel evolution of planispiral shells in a subclade of Truncatelloidea and enabled us to newly redefine the families Caledoniellidae, Elachisinidae, Teinostomatidae, Tornidae and Vitrinellidae.
Campagnes accessibles citées (2) [+] [-]
Codes des collections associés: IM (Mollusques) -
Innabi J., Stout C.C. & Valdés Á. 2023. Seven new “cryptic” species of Discodorididae (Mollusca, Gastropoda, Nudibranchia) from New Caledonia. ZooKeys 1152: 45-95. DOI:10.3897/zookeys.1152.98258
Résumé [+] [-]The study of a well-preserved collection of discodorid nudibranchs collected in Koumac, New Caledonia, revealed the presence of seven species new to science belonging to the genera Atagema, Jorunna, Rostanga, and Sclerodoris, although some of the generic assignments are tentative as the phylogeny of Discodorididae remains unresolved. Moreover, a poorly known species of Atagema originally described from New Caledonia is re-described and the presence of Sclerodoris tuberculata in New Caledonia is confirmed with molecular data. All the species described herein are highly cryptic on their food source and in the context of the present study the term “cryptic” is used to denote such species. This paper highlights the importance of comprehensive collecting efforts to identify and document well-camouflaged taxa.
Campagnes accessibles citées (3) [+] [-]
Codes des collections associés: IM (Mollusques) -
Irwin A.R., Strong E.E., Kano Y., Harper E.M. & Williams S.T. 2021. Eight new mitogenomes clarify the phylogenetic relationships of Stromboidea within the caenogastropod phylogenetic framework. Molecular Phylogenetics and Evolution 158: 107081. DOI:10.1016/j.ympev.2021.107081
Résumé [+] [-]Members of the gastropod superfamily Stromboidea (Littorinimorpha) are characterised by their elaborate shell morphologies, distinctive mode of locomotion, and often large and colourful eyes. This iconic group comprises over 130 species, including many large and charismatic species. The family Strombidae is of particular interest, largely due to its commercial importance and wide distribution in tropical and subtropical waters. Although a few strombid mitochondrial genomes have been sequenced, data for the other four Recent families in Strom boidea are lacking. In this study we report seven new stromboid mitogenomes obtained from transcriptomic and genomic data, with taxonomic representation from each Recent stromboid family, including the first mitoge nomes for Aporrhaidae, Rostellariidae, Seraphsidae and Struthiolariidae. We also report a new mitogenome for the family Xenophoridae. We use these data, along with published sequences, to investigate the relationships among these and other caenogastropod groups. All analyses undertaken in this study support monophyly of Stromboidea as redefined here to include Xenophoridae, a finding consistent with morphological and behav ioural data. Consistent with previous morphological and molecular analyses, including those based on mitoge nomes, monophyly of Hypsogastropoda is confirmed but monophyly of Littorinimorpha is again rejected.
Campagnes accessibles citées (4) [+] [-]
Codes des collections associés: IM (Mollusques) -
Kantor Y.I., Fedosov A.E., Kosyan A.R., Puillandre N., Sorokin P.A., Kano Y., Clark R. & Bouchet P. 2022. Molecular phylogeny and revised classification of the Buccinoidea (Neogastropoda). Zoological Journal of the Linnean Society 194(3): 789-857. DOI:10.1093/zoolinnean/zlab031
Résumé [+] [-]Abstract The superfamily Buccinoidea is distributed across the oceans of the world from the Arctic Ocean to the Antarctic and from intertidal to abyssal depths. It encompasses 3351 recent species in 337 genera. The latest taxonomic account recognized eight full families. For the first time, the monophyly of the superfamily and the relationships among the families are tested with molecular data supplemented by anatomical and radula data. Five genetic markers were used: fragments of mitochondrial COI, 16S rRNA, 12S rRNA and nuclear Histone 3 (H3) and 28S rRNA genes (for 225 species of 117 genera). Our analysis recovered Buccinoidea monophyletic in Bayesian analyses. The relationships between the formerly recognized families and subfamilies are drastically revised and a new classification of the superfamily is here proposed, now including 20 taxa of family rank and 23 subfamilies. Five new families (Chauvetiidae, Dolicholatiridae, Eosiphonidae, Prodotiidae and Retimohniidae) and one subfamily of Nassariidae (Tomliniinae) are described. Austrosiphonidae and Tudiclidae are resurrected from synonymy and employed in a new taxonomical extension. All but 40 recent genera are reclassified. Our results demonstrate that anatomy is rather uniform within the superfamily. With exceptions, the rather uniform radular morphology alone does not allow the allocation of genera to a particular family without additional molecular data.
Campagnes accessibles citées (42) [+] [-]ATIMO VATAE, AURORA 2007, BIOPAPUA, BOA1, CEAMARC-AA, CHALCAL 2, CONCALIS, CORSICABENTHOS 1, Restreint, Restreint, DongSha 2014, EBISCO, GUYANE 2014, ILES DU SALUT, INHACA 2011, KANACONO, KARUBENTHOS 2, KARUBENTHOS 2012, KAVALAN 2018, KOUMAC 2.1, KOUMAC 2.3, MADIBENTHOS, MAINBAZA, MIRIKY, MUSORSTOM 4, Restreint, NORFOLK 2, NanHai 2014, PANGLAO 2004, PANGLAO 2005, PAPUA NIUGINI, Restreint, SALOMON 2, SALOMONBOA 3, SANTO 2006, TAIWAN 2000, TAIWAN 2004, TARASOC, TERRASSES, Tuhaa Pae 2013, Restreint, ZhongSha 2015
Codes des collections associés: IM (Mollusques) -
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
Résumé [+] [-]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.
Campagnes accessibles citées (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
Codes des collections associés: IU (Crustacés)
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