-
Ahyong S.T. & Mihara E. 2000. Pisces Pleuronectiformes: Flatfishes from New Caledonia and adjacent waters. Genus Arnoglossus, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 21. Mémoires du Muséum national d'Histoire naturelle 184:783-813, ISBN:2-85653-526-7
Résumé [+]
[-]
Species of the bothid genus Arnoglossus collected from waters around New Caledonia are reviewed. Seven species,
including two new species, two new zoogeographical records and three species already recorded from the region were
identified, being Arnoglossus septemventralis sp. nov. and A. nigrifrons sp. nov., A. tenuis, A. elongatus, and A. macrolophus, A. japonicus and A. polyspilus, respectively. Arnoglossus septemventralis sp. nov., described from ten specimens collected between 230-315 m off southern New Caledonia, is easily separable from all other members of the genus in having seven pelvic rays on both sides. Arnoglossus nigrifrons sp. nov., described from two specimens collected from 300-315 m on the Chesterfield Plateau and northwest of New Caledonia, is characterized by a rounded upper head profile, several anterior dorsal fm rays elongated in males, gill rakers without serrations and a darkened head region.
Arnoglossus tenuis, collected from 10-16 m off New Caledonia, was previously known from southern Japan to the South
China Sea, and A. elongatus, from 250-350 m off New Caledonia, previously only from the Madura Sea and northwestern
Australia. Arnoglossus macrolophus was collected from relatively shallow waters (49-92 m) off New Caledonia, and A. japonicus and A. polyspilus from deeper waters (210-385 m) off New Caledonia, the Loyalty Islands and Chesterfield Plateau.
Campagnes accessibles citées (14) [+]
[-]
BATHUS 1,
BERYX 11,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
HALIPRO 1,
LAGON,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
SMIB 1,
SMIB 4,
SMIB 5,
SMIB 6
Codes des collections associés:
IC (Ichtyologie)
-
Anseeuw P. & Poppe G.T. 2001. Description of Perotrochus boucheti sp. nov. from the South Pacific (Gastropoda: Pleurotomariidae). Novapex 2(4): 125-131
Résumé [+]
[-]
P. boucheti is closely related to other Perotrochus species from the Indo-West Pacific such as P. africanus Tomlin, 1948, P. teramachii Kuroda, 1955, P. tangaroana Bouchet & Métivier, 1982 and P. westralis (Whitehead, 1987). Consistent differences in colour of teleoconch and base, sculptural pattern of basal disc and selenizone, shape of aperture and proportion of surface area covered by the umbilical region callus pad on basal disc allow separation on specific level. This represents the fourth species of living Perotrochus in the South Pacific.
Campagnes accessibles citées (12) [+]
[-]
BATHUS 3,
BERYX 11,
BIOCAL,
CHALCAL 2,
Restreint,
KARUBAR,
LITHIST,
MUSORSTOM 3,
MUSORSTOM 8,
SMIB 3,
SMIB 4,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Aznar-cormano L., Brisset J., Chan T., Corbari L., Puillandre N., Utgé J., Zbinden M., Zuccon D. & Samadi S. 2015. An improved taxonomic sampling is a necessary but not sufficient condition for resolving inter-families relationships in Caridean decapods. Genetica 143(2): 195-205. DOI:10.1007/s10709-014-9807-0
Résumé [+]
[-]
During the past decade, a large number of multi-gene analyses aimed at resolving the phylogeneticrelationships within Decapoda. However relationships among families, and even among sub-families, remain poorly defined. Most analyses used an incomplete and opportunistic sampling of species, but also an incomplete and opportunistic gene selection among those available for Decapoda. Here we test in the Caridea if improving the taxonomic coverage following the hierarchical scheme of the classification, as it is currently accepted, provides a better phylogenetic resolution for the inter-families relationships. The rich collections of the Muse´um National d’Histoire Naturelle de Paris are used for sampling as far as possible at least two species of two different genera for each family or subfamily. All potential markers are tested over this sampling. For some coding genes the amplification success varies greatly among taxa and the phylogenetic signal is highly saturated. This result probably explains the taxon-heterogeneity among previously published studies. The analysis is thus restricted to the genes homogeneously amplified over the whole sampling. Thanks to the taxonomic sampling scheme the monophyly of most families is confirmed. However the genes commonly used in Decapoda appear non-adapted for clarifying inter-families relationships, which remain poorly resolved. Genome-wide analyses, like transcriptome-based exon capture facilitated by the new generation sequencing methods might provide a sounder approach to resolve deep and rapid radiations like the Caridea.
Campagnes accessibles citées (39) [+]
[-]
Restreint,
ATIMO VATAE,
Restreint,
Restreint,
BATHUS 1,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BERYX 2,
BIOCAL,
Restreint,
BIOPAPUA,
Restreint,
Restreint,
Restreint,
Restreint,
Restreint,
Restreint,
HALIPRO 1,
HALIPRO 2,
Restreint,
KARUBAR,
Restreint,
LAGON,
MAINBAZA,
MD08 (BENTHOS),
MD20 (SAFARI),
MIRIKY,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 5,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
SALOMON 2,
SALOMONBOA 3,
SANTO 2006,
SMCB
Codes des collections associés:
IU (Crustacés)
-
Baba K. 2004. Uroptychodes, new genus of Chirostylidae (Crustacea: decapoda: Anomura) with description of three new species. Scientia Marina 68(1): 97-116
Résumé [+]
[-]
Examination of materials collected from Indonesia, New Caledonia and vicinity, now deposited in the Museum National d'Histoire Naturelle, disclosed three additional undescribed species of chirostylids belonging to the Uroplychus spinimarginatus group. The group is now shifted to a distinct genus Uroptychodes. Uroptychus grandirostris Yokoya, 1933, which can be transferred to Uroptychodes, has been a problematic species because of the brevity of the original description and the loss of the type material. However, a recent finding of a specimen, which is in poor condition, very much like the illustration of U. grandirostris by Yokoya (1933: Fig. 29), but different from the description of U. grandirostris given by van Dam (1939) for one of the type specimens, suggests that the type material of U. grandirostris includes at least two species. In this paper a neotype is selected for U. grandirostris. The genus Uroptychodes now contains 10 species. All these species are reviewed and a key to the species of the genus is provided.
Campagnes accessibles citées (7) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Baba K. 2018. Chirostylidae of the Western and Central Pacific: Uroptychus and a new genus (Crustacea: Decapoda: Anomura). Tropical Deep-Sea Benthos 30. Mémoires du Muséum National d'Histoire Naturelle 212, 612 pp. ISBN:978-2-85653-822-7
Campagnes accessibles citées (50) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
EBISCO,
GEMINI,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
SALOMON 1,
SALOMON 2,
SANTO 2006,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Bach P., Farinole F., Grandperrin R., Jomessy T., Mou-tham G. & Pantaloni L. 1999. Campagne ZoNéCo 6 de chalutages et de pêches à la palangre de fond dans l'ouest de la zone économique de Nouvelle-Calédonie (N.O. Alis de l'IRD, 1-14 décembre 1998). Rapport de campagne, IRD, 37 pp.
Résumé [+]
[-]
The exploratory fishing survey ZoNéCo 6 was canied out on board the R.Y. Alis of the IRD (Institut de Recherche pour le Développement) from 1-14 Décember 1998. lts main objective was to show whether commercial fish resources are present at depths between 300 and 800 m on the outer reef slopes of the Fairway-Lansdowne Bank and the Chesterfield Atoll. Two fishing techniques were used, bottom trawling and bottom longlining. The choice of fishing spots was based on both acoustic surveys using a 28 kHz FURUNO FCY 292 and the bathymetric charts produced during the seabed mapping survey ZoNéCo 4 canied out by the R.Y. L'Atalante. The duration of the trip was splitted into 41, l % devoted to transit, 27 % to bathymetry, 22.3 % to fishing and 9,6 % to waste of time due to bad weather conditions. 17 fishing stations were completed of which 9 were trawl hauls and 8 bottom longline sets amounting to a fishing effort close to 5000 hooks. Three trawl stations and 3 longline sets were made on the slopes of the Chesterfield Atoll whilst 6 trawl stations and 5 longline sets were completed on the slopes of the Fairway-Lansdowne Bank. The total catch was 822 kg of which 243 kg were caught with the trawl and 579 kg with the longline. The trawl did not catch any commercial species, shark amounting to 42 % of the catch, bone fishes 40 %, Crustaceans 9 % and Cephalopods 9 %. The average trawl catch rate was 0,6 tonne/km2 (6,06 kg/ha). The only commercial species caught with the longline were « red snappers» Etelis . carbunculus and E coruscans amounting to 211 kg (36,4 % of the total weight) with a catch rate of 4,3 kg/100 hooks. Sharks dominated the catch both in terms of number and weight (320 kg amounting to 55,3 % of the catch). Gnly one Beryx splendens was caught. With the exception of « red snappers », the survey did not show the presence of commercial target resources within the 300-800 m depth range of the prospected area.
Campagnes accessibles citées (6) [+]
[-]
-
Bailly N., Hureau J.C. & Pruvost P. 1999. Catalogue critique des types de poissons du Muséum national d'Hisqtoire naturelle (et des Musées d'Histoire naturelle en région). Ordre des Gadiformes. Cybium 23(3): 219-245
Résumé [+]
[-]
Ce catalogue recense les spécimens-types de l'ordre des Gadiformes (sensu Patterson et Rosen, 1989) dans les collections ichtyologiques du Muséum national d'histoire naturelle à Paris (MNHN), du Musée océanographique de Monaco (MOM), de l'Université Claude Bernard de Lyon (UCBL) et du Musée zoologique de Strasbourg (MZS).
Plusieurs articles traitant de la phylogénie des Gadiformes sont regroupés dans Cohen (1989). Les Zoarcoidei et les Ophidioidei ont été séparés des Gadiformes (voir Patterson et Rosen, 1989, pour un historique). Les premiers sont maintenant classés dans les Perciformes, les seconds dans un autre ordre de Paracantbopterygies, les Ophidiiformes
(Lecointre, 1994: Nelson. 1994). Les catalogues correspondant restent à compiler.
Le tableau 1 présente les récentes classifications des Gadiformes que nous avons
consultées (Markle in Cohen, 1989; Cohen et al. , 1990; Nelson, 1994). Nous les avons
comparées avec celles qui sont données par Eschmeyer (1990, 1998). Elles se recouvrent
très largement, abstraction faite du niveau taxinomique des catégories utilisées. Markle
les élève presque toutes au rang familial; Cohen et al. Ne distinguent ni les Steindachneriinae
ni les Ranicipitinae; par rapport à Cohen et al. (1990), Eschmeyer (1990) incluait
les Parabrotulidae dans les Gadiformes ( 1990), mais les place aujourd'hui dans les Ophidüdae
(Ophidiiformes) (1998) comme les autres auteurs. Et élève les Phycinae et les Lotinae
au rang familial. Néanmoins, la définition des Lotidae et des Phycidae varie d'un auteur
à l'autre (Tableau Il). La liste des Gadiformes actuels est en grande partie donnée dans
Cohen et al. (1990).
Les Gadiformes et les Pleuronectiformes sont les deux grands ordres de Poissons
qui n'ont pas été revus par Cuvier et Valenciennes dans leur monumental travail ( 1829-
1849). La liste des exemplaires historiques de l' annexe A comprend seulement des exemplaires
conservés en herbier. Provenant de Risso et d' Adan son, ainsi que quelques exemplaires
anciens conservés en alcool.
Les types d'herbier de Risso avaient été revus par Bertin (1945). Les types des
espèces de Macrouridae décrites par Vaillant en 1888 (Expéditions scientifiques du
"Travailleur" et du "Talisman") avaient été revus par Bauchot et al. (1972). Nous avons
intégralement repris leurs conclusions. Certains des types de Moridae ont été revus par
Cohen en 1964 et 1966, et par Paulin en 1989.
Campagnes accessibles citées (9) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Bamber R.N. 2004. Pycnogonids (Arthropoda: Pycnogonida) from French cruise to Menalesia. Zootaxa 551: 1-27
Résumé [+]
[-]
Seventy specimens of pycnogonid from New Caledonia and the Solomon Islands, collected during cruises from the Paris Museum, are described. No pycnogonids have been recorded previously from the Solomon Islands. Of the sixteen species identified, three ammotheids, Bathyzetes umbrella, Cilunculus cymobostrychos and C. mergus, are new to science. The distinctions of the sibling species Colossendeis pipetta Stock, 1991 and C. sinuosa Stock, 1997 are analyzed morphometrically. The pycnogonid fauna of the Melanesia-Micronesia-Polynesia region is summarized.
Campagnes accessibles citées (7) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Beu A.G. 1998. Indo-West Pacific Ranellidae, Bursidae and Personidae (Mollusca: Gastropoda). A monograph of the New Caledonian fauna and revisions of related taxa - Résultats des campagnes MUSORSTOM 19. Mémoires du Muséum national d'Histoire naturelle 178, 256 pp. ISBN:2-85653-517-8
Résumé [+]
[-]
The Ranellidae, Bursidae and Personidae from the New Caledonia region (including the Loyalty Islands, the Coral Sea and the New Hebrides Arc) are monographed based on the results of an extensive collecting effort totalling more than 1000 stations. Seventy-three species are recorded, with numerous range extensions. One of the more remarkable aspects of this fauna is the uniquely diverse deep-water tonnoidean assemblage, dominated by species such as Bursa fijiensis, B. latitudo, B. quirihorai, species of Distorsio, Sassia remensa, and less common small personids in the genera Distorsionella and Personopsis. The number of species of New Caledonian Personidae is the highest yet recorded. The Personopsis species are the first modem ones correctly referred to the genus. Revisions are provided of Biplex, Gyrineum, Cyinatium (Gelagna), the Cymatium vespaceum, C. tenuiliratum and Bursa latitudo species groups, of southwest Pacific species of Sassia, and of several Cymatium (Ranularia) and Distorsio species. New genera proposed are Halgyrineum (Ranellidae) and Distorsomina (Personidae). Seven new species are proposed: Biplex bozzettii (from Somalia and southem India), Gyrineum longicaudatum (from the tropical westem Pacific), Cymatium pemiiketi (from Oman), Distorsio parvimpedita, Distorsionella pseudaphera, Personopsis purpurata and P. trigonaperta (all from New Caledonia). The nomenclature of numerous taxa is stabilized by the designation of neotypes and lectotypes for nominal species named by A. Adams & Reeve, Broderip, Deshayes, Dillwyn, Dunker, Fulton, Gmelin, Gould, Gray, Iredale, Jousseaume, Kuenen. Küster, Lamarck, Linné, Martin. Mighels, d'Orbigny, Perry, Reeve, Röding, Salis Marschlins, Schepman, Schumacher, G B. Sowerby II, and Wood.
Campagnes accessibles citées (40) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
GEMINI,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
MD32 (REUNION),
MONTROUZIER,
MUSORSTOM 1,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMCB,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
SMIB 9,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Bouchet P. & Petit R.E. 2002. New species of deep-water Cancellariidae (Gastropoda) from the southwestern Pacific. The Nautilus 116(3): 95-104
Résumé [+]
[-]
One new genus and nine new species of Cancellariidae are described from New Caledonia from depths between 200 and 600 meters. They are: Africotriton adelphum new species, Mirandaphera new genus, Mirandaphera cayrei new species, Mirandaphera maestratii new species, Merica marisca new species, Sveltia rocroii new species, Sveltia splendidula new species, Nipponaphera pardalis new species, Nipponaphera cyphoma new species, and Nipponaphera goniata new species. Africotriton adelphum new species is the first species in that genus known from outside South Africa and Australia. The new genus Mirandaphera is characterized by its broad, non-umbilicate shell with very large crenulated axial ribs, and axial columella. The genus is composed of the new species described herein, Mirandaphera maestratii new species and M. cayrei new species, and two other species: M. tosaensis (Habe, 1961) new combination and M. arafurensis (Verhecken, 1997) new combination, from deep water off Japan and the Arafura Sea respectively. Trigonaphera teramachii Habe, 1961 and Agatrix. nodosivaricosa Petuch, 1979 are transferred to Nipponaphera. New species of Merica, Sveltia, and Nipponaphera are the deepest dwelling known representatives in their respective genera.
Campagnes accessibles citées (18) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CALSUB,
CHALCAL 2,
HALICAL 1,
HALIPRO 1,
LAGON,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 2,
SMIB 3,
SMIB 5,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Bouchet P. & Kantor Y.I. 2004. New Caledonia: The major centre of biodiversity for volutomitrid molluscs (Mollusca: Neogastropoda: Volutomitridae). Systematics and Biodiversity 1(4): 467-502. DOI:10.1017/S1477200003001282
Résumé [+]
[-]
Recent deep-sea explorations in the South Pacific have documented around New Caledonia the most diverse fauna of gastropods of the family Volutomitridae anywhere in the world. Fourteen species (nine new, two remaining unnamed) are recorded, all essentially confined to the 250–750 m depth range. The high number of species in the New Caledonia region does not appear to be an effect of sampling intensity, but appears to result from four factors: regional spatial heterogeneity, frequency of hard substrates, syntopy, and a historical heritage shared with Australia and New Zealand, which until now ranked as the major centre of volutomitrid diversity. In the New Caledonia region, volutomitrids show a marked preference for hard bottoms and up to three species may cooccur in the same dredge haul. Many species appear to have extremely narrow geographical distributions within the region (e.g. a single seamount or a single submerged plateau); conversely, Microvoluta joloensis, the only non-endemic volutomitrid present in New Caledonia, ranges from the Mozambique Channel to Tonga.
Campagnes accessibles citées (29) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
CORAIL 2,
HALICAL 1,
HALIPRO 1,
LAGON,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
NORFOLK 1,
PALEO-SURPRISE,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Bouchet P., Héros V., Lozouet P. & Maestrati P. 2008. A quarter-century of deep-sea malacological exploration in the South and West Pacific: Where do we stand? How far to go?, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:9-40, ISBN:978-2-85653-614-8
Résumé [+]
[-]
The Institut de Recherche pour le Développement (IRD, formerly ORSTOM) and Muséum national d’Histoire naturelle (MNHN) launched in the early 1980s a suite of oceanographic expeditions to sample the deep-water benthos of the tropical South and West Pacific, with emphasis on the 100-1,500 m bathymetric zone. This paper reviews the development of this programme to date. It describes the procedures involved in curating the material collected and the involvement of an international network of taxonomic experts to identify, describe and name the molluscan fauna. So far, 1,028 species of molluscs have been recorded from the New
Caledonia Exclusive Economic Zone from depths below 100 m, and 601 of these (58.4%) were new species. An additional 142 new species have been described from other South Pacifi c island groups (Solomon Islands, Vanuatu, Fiji, Wallis and Futuna, Tonga, Marquesas Islands and Austral Islands). However, the hyper-diverse families have essentially remained untouched. Regional differences among island groups are high, and New Caledonia, which has been sampled best, shows several discrete areas of micro-endemism.
We speculate that the deep-sea mollusc fauna of New Caledonia may amount to 15-20,000 species, and the corresponding number for the whole South Pacifi c may be in the order of 20-30,000 species.
Campagnes accessibles citées (63) [+]
[-]
AURORA 2007,
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CONCALIS,
CORAIL 2,
CORINDON 2,
GEMINI,
HALICAL 1,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
LUMIWAN 2008,
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 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
SMIB 9,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2004,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Boyer F. 2001. Espèces nouvelles de Marginellidae du niveau bathyal de la Nouvelle-Calédonie. Novapex 2(4): 157-169
Résumé [+]
[-]
Ten new species of Marginellidae are described from bathyal levels of New Caledonia and attributed to five different genera. The phyletic relationships dealt with recent or fossil close species are discussed.
Campagnes accessibles citées (6) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Boyer F. 2002. Description of five new marginellids from bathyal levels of southern New Caledonia. Novapex 3(2-3): 87-96
Résumé [+]
[-]
One species of Gibberula, three species of Dentimargo, and one species of Protoginella are described as new from bathyal levels south from New Caledonia. Dentimargo caledonicus (Cossignani, 2001) is redescribed and a new type locality is proposed. Some elements are given about the apparent distribution of the six species.
Campagnes accessibles citées (9) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Boyer F. 2008. The genus Serrata Jousseaume, 1875 (Caenogastropoda: Marginellidae) in New Caledonia, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:389-436, ISBN:978-2-85653-614-8
Résumé [+]
[-]
Thirty five species attributed to Serrata Jousseaume, 1875 are recognized from the bathyal zone of New Caledonia. Four of these, S. beatrix (Cossignani, 2001), S. tuii (Cossignani, 2001), S. stylaster (Boyer, 2001) and S. boucheti (Boyer, 2001), were previously described in other genera, and 31 other species are here described as new. This series of 35 Serrata species from New Caledonia increases
fi ve-fold the Recent specifi c diversity recognized in the genus. The diversity of Serrata species from New Caledonia is inferred to be very partially known, based on the fact that 31% of the identifi ed species are represented in the collections by only one specimen and that 51% were collected at only single stations. The important Serrata fauna documented here has an asymmetrical geographical
distribution in New Caledonia, the highest diversity of species being found off far southern New Caledonia and on the northern Norfolk Ridge. The Serrata fauna from New Caledonia, the Loyalty Ridge and the Norfolk Ridge appears to be isolated in the southwest Pacifi c, but it has affi nities with several species occurring in the fossil or Recent fauna of Australia and New Zealand. The fossil distribution of Serrata extends from the Eocene of Alabama to the Pliocene of New Zealand. The distribution of the genus in
the Recent seems to be restricted mostly to the southern Indo-Pacifi c latitudes from Cape Agulhas to the Tuamotu Islands, with maximum diversity from the Australian Platform to the Norfolk and New Caledonia Ridges. The fossil genera Euryentome Cossmann, 1899 and Conuginella Laseron, 1957 and the Recent genera Deviginella Laseron, 1957 and Serrataginella Coovert & Coovert, 1995 are proposed as junior synonyms of Serrata. Marginella anatina Lea, 1833 is used instead of Euryentome silabra Palmer, 1937 as the valid name for the type species of the genus Euryentome. The fossil genus Strombiginella Laseron, 1957 is placed in synonymy with the recent genus Hydroginella Laseron, 1957. Serrata and Hydroginella do not seem more closely related to each other than they are to Volvarina-Prunum or to the Austroginella and Dentimargo groups. The “Serrata Group” sensu Coovert & Coovert 1995, composed of Hydroginella, Serrata and 3 synonymous genera, is rejected as being a possibly polyphyletic assemblage. The high disparity in the specifi c shell morphologies of Serrata, the frequent combination of features found as typical in Volvarina and Dentimargo in the
Recent, the occurrence of many morphological intergrades between these genera since the Mid-Eocene of the western Tethys sea, and the higher specifi c frequency of the plesiomorphic character of a radula with numerous cusps, together suggest that the genus Serrata may be situated near the base of the common stem from which most of the Recent groups of the Volvarina-Dentimargo complex
have differentiated.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 2,
LAGON,
MUSORSTOM 4,
MUSORSTOM 6,
NORFOLK 1,
PALEO-SURPRISE,
SMIB 3,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Bracken-grissom H.D., Ahyong S.T., Wilkinson R.D., Feldmann R.M., Schweitzer C.E., Breinholt J.W., Bendall M., Palero F., Chan T., Felder D.L., Robles R., Chu K.H., Tsang L.M., Kim D., Martin J.W. & Crandall K.A. 2014. The Emergence of Lobsters: Phylogenetic Relationships, Morphological Evolution and Divergence Time Comparisons of an Ancient Group (Decapoda: Achelata, Astacidea, Glypheidea, Polychelida). Systematic Biology 63(4): 457-479. DOI:10.1093/sysbio/syu008
Résumé [+]
[-]
Lobsters are a ubiquitous and economically important group of decapod crustaceans that include the infraorders
Polychelida, Glypheidea, Astacidea andAchelata. They include familiar forms such as the spiny, slipper, clawed lobsters and crayfish and unfamiliar forms such as the deep-sea and “living fossil” species. The high degree of morphological diversity among these infraorders has led to a dynamic classification and conflicting hypotheses of evolutionary relationships. In this study, we estimated phylogenetic relationships among the major groups of all lobster families and 94% of the genera using six genes (mitochondrial and nuclear) and 195 morphological characters across 173 species of lobsters for the most comprehensive sampling to date. Lobsters were recovered as a non-monophyletic assemblage in the combined (molecular + morphology) analysis. All families were monophyletic, with the exception of Cambaridae, and 7 of 79 generawere recovered as poly- or paraphyletic. A rich fossil history coupled with dense taxon coverage allowed us to estimate and compare divergence times and origins of major lineages using two drastically different approaches. Age priors were constructed and/or included based on fossil age information or fossil discovery, age, and extant species count data. Results from the two approaches were largely congruent across deep to shallow taxonomic divergences across major lineages. The origin of the first lobster-like decapod (Polychelida) was estimated in the Devonian (∼409–372 Ma) with all infraorders present in the Carboniferous (∼353–318 Ma). Fossil calibration subsampling studies examined the influence of sampling density (number of fossils) and placement (deep, middle, and shallow) on divergence time estimates. Results fromour study suggest including at least 1 fossil per 10 operational taxonomic units (OTUs) in divergence dating analyses.
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Buckeridge J.S. 1998. A new coral inhabiting barnacle of the genus Chionelasmus (Cirripedia, Balanomorpha) from New Caledonia, Southwest Pacific. Zoosystema 20(2): 167-176
Résumé [+]
[-]
This paper describes Chionelasmus crosnieri n. sp., from a guyot on the northern part of Norfolk Ridge, to the south of New Caledonia. This new species, within the previously monospecific genus Chionelasmus, inhabits a living octoral, Muricides sp. indet. Comments on the distribution and habitat of the new species are provided, including a proposal for the method by which the cyprid larva of C. crosnieri gained access to the axial skeleton of the octocoral.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Burukovsky R.N. 2000. Taxonomy of Nematocarcinus (Decapoda, Nematocarcinidae). 3. Description of new species. Zoologicheskii Zhurnal 79(6): 662-668
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Cairns S. & Kitahara M. 2012. An illustrated key to the genera and subgenera of the Recent azooxanthellate Scleractinia (Cnidaria, Anthozoa), with an attached glossary. ZooKeys 227: 1-47. DOI:10.3897/zookeys.227.3612
Résumé [+]
[-]
The 120 presently recognized genera and seven subgenera of the azooxanthellate Scleractinia are keyed using gross morphological characters of the corallum. All genera are illustrated with calicular and side views
of coralla. All termes used in the key are defined in an illustrated glossary. A table of all species-level keys,
both comprehensive and faunistic, is provided covering the last 40 years.
Campagnes accessibles citées (21) [+]
[-]
BATHUS 1,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CONCALIS,
EBISCO,
HALIPRO 2,
LAGON,
LIFOU 2000,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
SMIB 10,
SMIB 5,
TERRASSES
Codes des collections associés:
IK (Cnidaires)
-
Castelin M., Puillandre N., Lozouet P., Sysoev A., Richer de forges B. & Samadi S. 2011. Molluskan species richness and endemism on New Caledonian seamounts: Are they enhanced compared to adjacent slopes?. Deep Sea Research Part I: Oceanographic Research Papers 58(6): 637-646. DOI:10.1016/j.dsr.2011.03.008
Résumé [+]
[-]
Seamounts were often considered as‘hotspots of diversity’ and ‘centers of endemism’,but recently this opinion has been challenged. After 25 years of exploration and the work of numerous taxonomists, the Norfolk Ridge (Southwest Pacific) is probably one of the best-studied seamount chains worldwide.
However,even in this intensively explored area, the richness and the geographic patterns of diversity
are still poorly characterized. Among the benthic organisms,the post-mortem remains of mollusks can supplement live records to comprehensively document geographical distrbutions. Moreover, the
accretionary growth of mollusk shells informs us about the lifes pan of the pelagic larva.To compare
diversity and level of endemism between the Norfolk Ridge seamounts and the continental slopes of
New Caledonia we used species occurrence data drawn from (i) the taxonomic literature on mollusks
and (ii) a raw dataset of mainly undescribed deep-sea species of the hyperdiverse Turridae. Patterns of endemism and species richness were analyzed through quantitative indices of endemism and species richness estimates or metrics.To date, 403 gastropods and bivalves species have been recorded on the Norfolk Ridge seamounts. Of these, at least 38 species(10%) are potentially endemic to the seamounts
and nearly all of 38 species have protoconchs indicating lecithotrophic larval development. Overall, our results suggest that estimates of species richness and endemism ,when sampling effort is taken into account, were not significantly different between slopes and seamounts. By including in our analyses
347 undescribed morphospecies from the Norfolk Ridge, our results also demonstratet he influence of
taxonomic bias on our estimates of species richness and endemism.
Campagnes accessibles citées (16) [+]
[-]
AZTEQUE,
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOCAL,
CHALCAL 2,
HALIPRO 2,
LITHIST,
NORFOLK 1,
NORFOLK 2,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
TERRASSES
Codes des collections associés:
IM (Mollusques)
-
Castro P. 1997. Trapeziid crabs (Brachyura: Xanthoidea: Trapeziidae) of New Caledonia, eastern Australia and the Coral Sea, Les fonds meuble des lagons de Nouvelle-Calédonie (Sédimentologie, Benthos) 3. Etudes et thèses:59-107
Résumé [+]
[-]
An examination of extensive collections made in New Caledonia and nearby islands by the ORSTOM Center in Nouméa, New Caledonia, of collections kept at various museums, and collections of live material made by the author in New Caledonia and in Queensland, Australia, has revealed that a total of 20 species belonging to five genera of trapeziid crabs inhabit the Coral Sea region. Two of the species belonging to the genus Trapezia are described as new. The taxonomic status of several species, particularly Trapezia cymhce (Herbst, 1801), is also revised.
Campagnes accessibles citées (18) [+]
[-]
BATHUS 2,
BATHUS 3,
BERYX 11,
CALSUB,
CHALCAL 1,
CORAIL 2,
GEMINI,
HALIPRO 1,
LAGON,
MONTROUZIER,
MUSORSTOM 2,
MUSORSTOM 6,
MUSORSTOM 8,
Restreint,
SMIB 1,
SMIB 3,
SMIB 8,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Castro P. 2000. Crustacea Decapoda: A revision of the Indo-West Pacific species of palicid crabs (Brachyura Palicidae)), in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 21. Mémoires du Muséum national d'Histoire naturelle 184:437-610, ISBN:2-85653-526-7
Résumé [+]
[-]
The taxonomy of the crabs belonging to the family Palicidae Bouvier, 1898 from the Indo-west Pacific region is revised. On the basis of extensive material collected by French expeditions in the Coral Sea and other regions of the Pacific and Indian oceans, as well as material from numerous museums, including most of the types, the present study recognizes two subfamilies, 10 genera, and 43 species. Of these taxa, four are new genera: Exopalicus, Miropalicus, Paliculus, and Rectopalicus. Manella is synonymized with Crossotonotus A. Milne Edwards, 1873. Parapleurophricoides Nobili, 1906, sometimes believed to be a palicid, is a xanthoid and it is removed from the Palicidae. Nine nominal species described by previous authors are synonymized and an additional 17 species are described.
Campagnes accessibles citées (36) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
LITHIST,
MONTROUZIER,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
Restreint,
SMCB,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Castro P., Williams A.B. & Cooper L.L. 2003. Revision of the family Latreilliidae Stimpson, 1858 (Crustacea, Decapoda, Brachyura). Zoosystema 25(4): 601-634
Campagnes accessibles citées (32) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
Restreint,
CORINDON 2,
HALIPRO 1,
KARUBAR,
LAGON,
LIFOU 2000,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
MUSORSTOM 9,
PALEO-SURPRISE,
SMIB 4,
SMIB 5,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Castro p. 2007. A reappraisal of the family Goneplacidae MacLeay, 1838 (Crustacea, Decapoda, Brachyura) and revision of the subfamily Goneplacinae, with the description of 10 new genera and 18 new species. Zoosystema 29(4): 609-774
Résumé [+]
[-]
A reappraisal of the taxonomy of the brachyuran crabs belonging to the family Goneplacidae MacLeay, 1838 sensu lato has resulted in the revision of the subfamily Goneplacinae, which combines the subfamilies Goneplacinae MacLeay, 1838 and Carcinoplacinae H. Milne Edwards, 1852. Most of the 66 species of Goneplacinae sensu stricto that are listed herein inhabit relatively deep water and are infrequently collected. The subfamily Goneplacinae sensu stricto now consists of 17 genera of which 10 are being described as new: Carcinoplax H. Milne Edwards, 1852, with 18 species of which four are new; Entricoplax n. gen., monotypic; Exopheticus n. gen., with two species; Goneplacoides n. gen., monotypic; Goneplax Leach, 1814, with four species; Hadroplax n. gen., monotypic; Menoplax n. gen., monotypic; Microgoneplax n. gen., with five species of which four are new; Neogoneplax n. gen., with three species of which two are new; Neommatocarcinus Takeda & Miyake, 1969, monotypic; Notonyx A. Milne-Edwards, 1873, with three species; Ommatocarcinus White, 1852, with four species; Paragoneplax n. gen., monotypic; Psopheticus Wood-Mason, 1892, with four species; Pycnoplax n. gen., with five species of which one is new; Singhaplax Serene & Soh, 1976, with seven species of which four are new; and Thyraplax n. gen., with five species of which three are new. All goneplacine genera are exclusive to the Indo-West Pacific region (plus contiguous temperate areas) except Goneplax, which is so far known mostly from the Atlantic and Mediterranean regions. Four nominal species described by other authors were found to be junior subjective synonyms for other species: Carcinoplax verdensis Rathbun, 1914 and C polita Guinot, 1989 synonymous of C specularis Rathbun, 1914; Goneplax megalops Komatsu & Takeda, 2003 of Goneplacoides marivenae (Komatsu & Takeda, 2003) n. comb.; and Psopheticus insolitus Guinot, 1990 of P stridulans Wood-Mason, 1892.
Campagnes accessibles citées (44) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
EBISCO,
HALIPRO 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
PANGLAO 2004,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
SMCB,
SMIB 3,
SMIB 5,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2004,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Cecalupo A. & Perugia I. 2017. Cerithiopsidae and Newtoniellidae (Gastropoda: Triphoroidea) from New Caledonia, Western Pacific. Visaya Suppl. 7: 1-175
Campagnes accessibles citées (17) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BERYX 11,
CORAIL 2,
EBISCO,
LAGON,
LIFOU 2000,
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 6,
NORFOLK 1,
NORFOLK 2,
PALEO-SURPRISE,
SANTO 2006,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Chan T. 2004. The ‘‘Plesionika rostricrescentis (Bate, 1888)’’ and ‘‘P. lophotes Chace, 1985’’ species groups of Plesionika Bate, 1888, with descriptions of five new species (Crustacea: Decapoda: Pandalidae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:293-318, ISBN:2-85653-557-7
Résumé [+]
[-]
Before the present study, Plesionika rostricrescentis (Bate, 1888) and P. lophotes Chace, 1985 were the two Plesionika species unique in having a high basal rostral crest. A recently described species, P. erythrocyclus Chan & Crosnier, 1997 has a low basal rostral crest but is evidently related to P. rostricrescentis. Close examination of the abundant material collected during the MUSORSTOM expeditions and from Taiwan revealed that there are at least eight species in this ‘‘P. rostricrescentis-P. lophotes’’ species complex. These taxa are morphologically very similar but can be distinguished by their very distinctive colorations, which are often striking and consist of large circular spots. In the ‘‘P. rostricrescentis’’ group, which has the dorsal margin of the rostrum unarmed between the anteriormost tooth of the basal rostral crest and the subapical teeth, five species are recognized. Plesionika rostricrescentis is still known only by the holotype from the Kai Islands. Two new species, P. hsuehyui and P. suffusa, closely similar to P. rostricrescentis, are described. Plesionika hsuehyui is widely distributed from Taiwan to Fiji, while P. suffusa has only been found off New Caledonia. Plesionika erythrocyclus, previously known only from Taiwan and French Polynesia, occurs widely in the southern Pacific. Another new species, P. bimaculata, which closely resembles P. erythrocyclus, is distributed off New Caledonia and in adjacent areas. Three species are recognized in the ‘‘P. lophotes’’ group, which bear dorsal rostral teeth between the basal rostral crest and subapical teeth. Plesionika lophotes is restricted to the area between Japan and northwestern Australia. Two further closely similar new species, P. rufomaculata and P. scopifera are described, the former widely distributed from Okinawa to Futuna Island, the latter only off New Caledonia and Tonga. Although coloration is very important in distinguishing these species, species with similar color patterns do not necessarily belong to the same species group. Morphologically, these species are mainly separated by the height of the basal rostral crest, the number of rostral teeth, and the length of the stylocerite and the dactyli of the posterior three pereiopods. However, there is sexual dimorphism in the development of the basal rostral crest in these species, sometimes making positive identification of males and young specimens difficult.
Campagnes accessibles citées (29) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
HALICAL 1,
LAGON,
LITHIST,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
VOLSMAR
Codes des collections associés:
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (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,
Restreint,
EBISCO,
EXBODI,
HALIPRO 1,
KARUBAR,
LITHIST,
MAINBAZA,
Restreint,
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
Codes des collections associés:
IU (Crustacés)
-
Cleva R. 1997. Crustacea Decapoda : Stylodactylidae récoltés en Indonésie, aux îles Wallis et Futuna et au Vanuatu (campagne KARUBAR, MUSORSTOM 7 et 8). Données complémentaires sur les Stylodactylidae de Nouvelle-Calédonie, in Crosnier A. & Bouchet P.(Eds), Campagne Franco-Indonésienne KARUBAR - Résultats des campagnes MUSORSTOM 16. Mémoires du Muséum national d'Histoire naturelle 172:385-407, ISBN:2-85653-506-2
Résumé [+]
[-]
During the French-Indonesian expedition KARUBAR off Kai and Tanimbar Islands (Moluccas) in 1991, eight species of Stylodactylidae were collected. One of these species, Parastylodactylus moluccensis was new. Two other species, Parastylodactylus richeri Cleva, 1990, and Neostylodactylus affinis Hayashi & Miyake, 1968, are recorded from the region for the first time and the remaining five species, Stylodactylus tokarensis Zarenkov, 1968, S. multidentatus Kubo, 1942, S. libratus Chace, 1983, Parastylodactylus bimaxillaris (Bate, 1888), and Stylodactylus licinus Chace, 1983, are already known from the Indonesian area, the last one having been recorded recently by TAKEDA and HANAMURA (1994).
On the other hand, some specimens, at first identified doubtfully as Stylodactylus libratus, and related to Stylodactylus pubescens Burukovsky, 1990, have been causing trouble to us, and we have not find till now a satisfying solution: they are mentionned here as Stylodactylus sp. Stylodactylus brevidactylus Cleva, 1990, considering the variability observed through 49 specimens of S. multidentatus Kubo collected during this cruise, is synonymised with this species.
We added to the indonesian material, for each different species, the specimens collected recently from Wallis and Futuna, the Vanuatu and New-Caledonia. The species from these three countries which have not been collected during the KARUBAR expedition are mentionned at the end of this study.
Campagnes accessibles citées (13) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 2,
HALIPRO 1,
KARUBAR,
MONTROUZIER,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 8
Codes des collections associés:
IU (Crustacés)
-
Cleva R. 2004. Stylodactylidae and Bathypalaemonellidae from Taiwan (Crustacea: Decapoda: Caridea). Raffles Bulletin of Zoology 52(2): 497–511
Résumé [+]
[-]
Seven shrimp species of the family Stylodactylidae are reported here from Taiwanese waters, four of which represent new records for the area. Only three species of this family were previously known from Taiwan: Stylodactylus in multidentatus Kubo, 1942, and Parastylodactylus bimaxillaris (Bate, 1888), both present in the collection studied here, and Bathystylodactylus inflatus Hanamura & Takeda, 1996, no material in the present collection. Stylodactylus major Hayashi & Miyake, 1968, is recorded for the second time. The other species are: Stylodactylus libratus Chace, 1983, Stylodactylus licinus Chace, 1983, and Stylodactylus tokarensis Zarenkov, 1968. On another hand, the status of a seventh species, related to Stylodactylus pubescens Burukovsky 1990, is left unresolved. The rare deep-sea shrimp family Bathypalaemonellidae is added to the Taiwanese decapod fauna, being represented by four species, one of which is new: Bathypalaemonella hayashii Komai, 1995; Bathypalaemonetes brevirostris (Bruce, 1986); Bathypalaemonetes pilosipes (Bruce, 1986) and Bathypalaemonetes chani, new species.
Campagnes accessibles citées (19) [+]
[-]
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
KARUBAR,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 4,
MUSORSTOM 8,
MUSORSTOM 9,
SALOMON 1,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2003
Codes des collections associés:
IU (Crustacés)
-
Cleva R., Guinot D. & Albenga L. 2007. Annotated catalogue of brachyuran type specimens (Crustacea, Decapoda, Brachyura) deposited in the Muséum national d’Histoire naturelle, Paris. Part I. Podotremata. Zoosystema 29(2): 229-279
Résumé [+]
[-]
The greatest part of the types of the brachyuran crabs (Crustacea, Decapoda) in the Crustacea collection of the Museum national d'Histoire naturelle, Paris, is already catalogued on registers and is to be gradually published. This first annotated catalogue lists the nominal species belonging to the Podotremata (i.e. crabs with coxal male and female gonopores, and spermathecae): families Homolodromiidae, Dromiidae, Dynomenidae, Homoliclae, Poupiniidae, Cycloclorippidae, Cymonomidae, Phyllotymolinidae and Raninidae. The names of the taxa are presented in their original combination. The erroneous references to specimens as "types" have been noted and corrected in conformity with the International Code of Zoological Nomenclature. The types of a total of 104 species are listed herein, out of about 370 known species of podotreme crabs. Photographs of most of the type specimens are also provided. A bibliography and an index are included.
Campagnes accessibles citées (35) [+]
[-]
Restreint,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BENTHEDI,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
HALICAL 1,
KARUBAR,
LAGON,
LIFOU 2000,
MD32 (REUNION),
Restreint,
MUSORSTOM 1,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
Restreint,
SALOMON 1,
SMCB,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6
Codes des collections associés:
IU (Crustacés)
-
Crosnier A. 1994. SPHAERODROMIA LAMELLATA ESPECE NOUVELLE DE NOUVELLE-CALEDONIE (DECAPODA, BRACHYURA, DROMIIDAE). Crustaceana 67(3): 341-348
Résumé [+]
[-]
A new species belonging to the genus Spkaerodromia, S. lamellata, is described. It was caught by trawling off the SE of New Caledonia at a depth of 400 m. This species can be recognized, at first glance, from the four other species of the genus by the lamellated anterolateral margins of the carapace.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Crosnier A. 1997. Crustacea Decapoda : Pseudopandalus curvirostris, genre et espèce nouveaux (Pandalidae) de Nouvelle Calédonie, Résultats des campagnes MUSORSTOM 18. Mémoires du Muséum national d'Histoire naturelle 176:169-176, ISBN:2-85653-511-9
Campagnes accessibles citées (10) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Crosnier A. 2002. Révision du genre Parathranites Miers, 1886 (Crustacea, Brachyura, Portunidae). Zoosystema 24(4): 799-825
Résumé [+]
[-]
Based on rather abundant material from the Indo-West Pacific, the number of species in the genus Parathranites Miers, 1886 is elevated from two to eight. The six new species are P. granosus n. sp., P. tuberosus n. sp., P. tuberogranosus n. sp., P. ponens n. sp., P. intermedius n. sp. and P. parahexagonum n. sp. Examination of the type series of the type species for the genus, P. orientalis Miers, 1886, shows that it contains two species; a lectotype is designated for P. orientalis. The main morphological characters used for differentiating the species are the breadth/length ratio of the carapace (correlated with the length of the fifth anterolateral teeth of the carapace) which can vary from 1.3 to 2.1, the presence or absence of a median tubercle on the posterior part of the cardiac area, the granulation of the carapace and the shape of the first male pleopods. An identification key for members of this genus is proposed.
Campagnes accessibles citées (23) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
HALIPRO 1,
KARUBAR,
LAGON,
LITHIST,
MD32 (REUNION),
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
PALEO-SURPRISE,
SMCB,
SMIB 6,
TAIWAN 2000
Codes des collections associés:
IU (Crustacés)
-
Crosnier A. & Dall W. 2004. Redescription of Hymenopenaeus obliquirostris (Crustacea, Decapoda, Penaeoidea, Soleneceridae) and descriptions of two new species of Hymenopenaeus from the Indo-West Pacific. Zootaxa 600: 1-26
Résumé [+]
[-]
Hymenopenaeus obliquirostris ( Bate, 1881), a relatively poorly known species, is redescribed, figured and compared with H. halli Bruce, 1966. Two other species of Hymenopenaeus, H. methalli from the southwest Pacific and H. fallax from Hawaii, are described as new. All these species are closely related to one another. They are distinguished essentially by the presence or absence of a postrostral carina, the presence or absence of a fixed spine on the merus of the first pereopods, and the shape of parts of the thelycum and petasma.
Campagnes accessibles citées (12) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 2,
HALIPRO 1,
HALIPRO 2,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8
Codes des collections associés:
IU (Crustacés)
-
Crosnier A. 2006. Penaeopsis Bate, 1881 (Crustacea, Decapoda, Penaeidae) récoltées dans le Pacifique sud-ouest par les campagnes françaises depuis 1976. Description d'une espèce nouvelle. Zoosystema 28(2): 331-340
Résumé [+]
[-]
Penaeopsis (Crustacea, Decapoda, Penaeidae) collected in the south-west Pacific by French expeditions since 1976. Description of a new species. This work is based on collections made in the south-west Pacific by IRD (ex ORSTOM) and the Museum national d'Histoire naturelle, Paris. It deals with four species of Penaeopsis Bate, 188 1: P challengeri de Man, 1911, P eduardoi Perez Farfante, 1977, P rectacuta (Bate, 188 1), and a new species, P mclaughlinae n. sp. Depth zones and geographic distributions of the three known species are revised, especially those of P challengeri. Penaeopsis mclaughlinae n. sp. is closely related to P eduardoi but it is easily distinguished by the more sinuous shape of the distal part of the ventrolateral lobules of the petasma, and the large rounded protuberance on the median plate of the thelycum.
Campagnes accessibles citées (26) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
CORINDON 2,
HALIPRO 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
PALEO-SURPRISE,
SALOMON 1,
SMIB 10
Codes des collections associés:
IU (Crustacés)
-
Crosnier a. 2001. Grapsidae (Crustacea, Decapoda, Brachyura) d’eau profonde du Pacifique sud-ouest. Zoosystema 23(4): 783-796
Campagnes accessibles citées (21) [+]
[-]
AZTEQUE,
BATHUS 2,
BATHUS 3,
BERYX 11,
BERYX 2,
CHALCAL 2,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 3,
MUSORSTOM 4,
SMCB,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Crosnier a. 2003. Sicyonia (Crustacea, Decapoda, Penaeoidea, Sicyoniidae) de l’Indo-ouest Pacifique. Zoosystema 25(2): 197-348
Résumé [+]
[-]
This work deals with 31 species of Sicyonia H. Milne Edwards, 1830, based on the collections made by the IRD (ex ORSTOM) and the Museum national d'Histoire naturelle, Paris, and on the collections of 28 other museums. Nineteen species are considered valid: S. australiensis Hanamura Wadley, 1998; S. benthophila de Man, 1907; S. bispinosa de Haan, 1850; S. curvirostris Balss, 1913; S. fallax de Man, 1907; S. furcata Miers, 1878; S. inflexa (Kubo, 1949); S. japonica Balss, 1914; S. laevis Bate, 1881; S. lancifer (Olivier, 1811); S. longicauda Rathbun, 1906; S. nasica Burukovsky, 1990; S. ocellata Stimpson, 1860; S. parafallax Crosnier, 1995; S. parvula de Haan, 1850; S. rectirostris de Man, 1907; S. trispinosa de Man, 1907; S. truncata (Kubo, 1949) and S. vitulans (Kubo, 1949). Four species are considered to be synonyms: S. cristata (de Haan, 1844) = S. lancifer; S. formosa (Chan & Yu, 1985) = S. furcata; S. ommanneyi Hall, 1961 = S. ocellata; S. nebulosa Kubo, 1949 = S. laevis. Twelve species are described as new: S. abathophila n. sp., S. adunca n. sp., S. altirostrum n. sp., S. dejouanneti n. sp., S. komai n. sp., S. longicornis n. sp., S. metavitulans n. sp., S. parajaponica n. sp., S. robusta n. sp., S. rocroi n. sp., S. rotunda n. sp. and S. taiwanesis n. sp. Some forms, near S. australiensis and S. dejouanneti n. sp., are mentioned but not named because the material available is insufficient. An attempt is made to classify the Indo-West Pacific species of Sicyonia into eight groups. Some groups are coherent, while others are certainly artificial. Some species cannot be placed in any of the groups and the placement of several species known from one sex only remains hazardous. An identification key is presented. Particular care was taken in illustrating the genitalia, which provide the most important characters for recognizing the species. Colour photographs show the coloration of living specimens of 17 species. Depth zones and geographic distributions of all the species are presented in tabular form. As with previous studies, high species diversity of the Philippines-Indonesia fauna is evident, as well as the reduction of the number of species when one moves away from the area, except for New Caledonian area because of the unusually high h density of the samples collected in this area.
Campagnes accessibles citées (49) [+]
[-]
Restreint,
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
MONTROUZIER,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
PALEO-SURPRISE,
Restreint,
Restreint,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
SMIB 9,
Restreint,
TAIWAN 2000,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
D'auria V., Giannini C., Minale L., Zampella A., Debitus C. & Frostin M. 1997. Bengamides and Related New Amino Acid Derivatives from the New Caledonian Marine Sponge Jaspis carteri. Journal of natural products 60(8): 814-816
Résumé [+]
[-]
Five new amino acid derivatives were isolated from the New Caledonian sponge Jaspis carteri, together with known bengamides A and B. The structures of the new compounds were determined by interpretation of their spectral data and by comparison with spectral data of known bengamides. Compounds 4-7 are simply the tridecanoate and pentadecanoate analogues of the original bengamides A and B, whereas compound 8 is a caprolactam formamide derivative of bengamide B.
Campagnes accessibles citées (2) [+]
[-]
Codes des collections associés:
IP (Porifères)
-
De saint laurent M. & Mclaughlin P.A. 1999. A new genus and species of hermit crabs (Decapoda, Anomura, Paguridae) from the western Pacific. Zoosystema 21(1): 77-92
Résumé [+]
[-]
A new genus is porposed for a new species widely distributed in the western Pacific Ocean from the Philippine Islands in the northwestern Pacific south to Kermadec Islands of New Zeland. Jacquesia n. genus, bears considerable similarity to Iridopagurus de Saint Laurent-Dechancé, 1966, in lacking an accessory tooth on the crista dentata of the third maxilliped, but having eleven pairs of quadriserial gills, slender elongate and subequal chelipeds and a well-developed left male sexual tube. It is distinguished from Iridopagurus by he presence of paired fisrt pleopods in females. The new species is a very distinct, but morphologically variable species. Theses variations, however, do not appear to be correlated with either size or sex.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 4,
BERYX 11,
CHALCAL 1,
CHALCAL 2,
HALICAL 1,
MUSORSTOM 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Del cerro L. & Lloris D. 1997. Gurnard Fishes (Scorpaeniformes, Triglidae) from off New Caledonia with description of five new species, in Séret B.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:91-124, ISBN:2-85653-500-3
Campagnes accessibles citées (8) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Dijkstra H.H. 2001. Bathyal Pectinoidea (Bivalvia: Propeamussiidae, Entoliidae and Pectinidae) from Wallis and Futuna Islands, Vanuatu Archipelago and New Caledonia, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:73-95, ISBN:2-85653-527-5
Résumé [+]
[-]
Material from recent expeditions off Vanuatu and Wallis and Futuna islands (NE of Fiji) include new records of deep water Pectinoidea. The 20 species recorded from Vanuatu are shared with New Caledonia (80%), Indonesia (70%) and Wallis and Futuna (60%), and the 24 species recorded from Wallis and Futuna are shared with New Caledonia (75%), Indonesia (63%) and Vanuatu (54%). Parvamussium musorstomi sp. novo is described from Wallis and Futuna. The New Caledonia records of Propeamussium maorium are revised and reidentified as P. investigatoris. Parvamussium cristatellum and Propeamussium siratama are recorded and P. richeri sp. novo is described from New Caledonia. A lectotype is designated for Propeamussiwn jefjreysii.
Campagnes accessibles citées (10) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Dolin L. 2001. Les Triviidae (Mollusca : Caenogastropoda) de l’Indo-Pacifique : Révision des genres Trivia, Dolichupis et Trivellona, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep-Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:201-241, ISBN:2-85653-527-5
Résumé [+]
[-]
The Indo-Pacific species of Trivia, Dolichupis and Trivellona are revised, based on the most abundant and
comprehensive material ever brought together and reveals a previously unsuspected diversity of Triviinae in the upper
bathyal zone (200-500 m) of the tropical West Pacific. The description of this fauna gives an opportunity to reevaluate
the validity of numerous species- and genus-group taxa recognized earlier, both in the littoral and deep water zones. The
present paper deals with Trivia Broderip, 1837, Decoriatrivia Cate, 1979, Dolichupis Iredale, 1930, and Trivellona
Iredale, 1931. A forthcoming study will deal with Trivirostra Jousseaume, 1884, Cleotrivia Iredale, 1930, and Semitrivia
Cossmann, 1903. By First Reviser action, Ellatrivia Iredale, 1931 is given precedence over Fossatrivia Iredale, 193 I . Decoriatrivia is treated as a subgenus of Trivia; Dolichupis is regarded as generically distinct from Pusula; the nominal
genus Pseudotrivia is synonymized with Trivellona. Trivia (T.) cylindrica sp. novo from the Philippines, and Trivia (T.)
vitrosphaera sp. nov., from New Caledonia, represent the first records of Trivia (T.) in the Indo-Pacific. Their deep-water
occurrence contrasts with that of the six or so species from the littoral of the temperate and tropical eastern Atlantic.
Dolichupis malvabasis sp. nov., a deep water species from the Philippines, is closely related to the type species and sole
other representative of Dolichupis, D. producta (Gaskoin, 1836). Nine named and six new species are recognized in
Trivellona: T. bulla sp. nov., T. conjonctiva sp. nov., T. oligopleura sp. nov., T. syzygia sp. novo and T. galea sp. nov.,
all from New Caledonia, and T. eglantina sp. novo from the Philippines. Trivia valerieae Hart, 1996 [= Erato tetatua Hart,
1996, syn. Nov.; First Reviser] is treated as a SW Pacific subspecies of T. paucicostata (Schepman, 1909); T.
Shimajiriiensis McNeil, 1961, described from the Pliocene of Okinawa, is now recorded in the Recent fauna of the
Philippines. Pusula niasensis Wissema, 1948 is a new synonym of Dolichupis producta (Gaskoin, 1836), Pseudotrivia
sagamiensis KUI'oda & Habe, 1971 is a new synonym of T. sibogae (Schepman, 1909), and Fossatrivia suduirauti Lorenz,
1996 is a new synonym of T. speciosa (Kuroda & Cate, 1979). Three nominal species described by Cate (1979)
supposedly from the Philippines are shown to be wrongly localized and synonyms of Atlantic taxa: Pseudotrivia
samarensis is synonymized with Trivia (T.) arctica (Pulteney, 1799) from Europe, and Pseudotrivia dumaliensis and
Niveria (Cleotrivia) aquatanica are both synonymized with Niveria (N) nix Schilder, 1922 from the Caribbean.
Decoriatrivia halians Cate, 1979 and D. but'ius Cate, 1979 are both synonymized with Trivia (Decoriatrivia) pauci!irata
Sowerby, 1870 from the Panamic Province.
Campagnes accessibles citées (27) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
GEMINI,
KARUBAR,
LAGON,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Duhamel G. 1997. Notopogon xenosoma Regan, 1914 (Teleostei, Macroramphosidae) en limite de distribution subtropicale aux abords de la Nouvelle-Calédonie et de Madagascar, in Séret B.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:83-89, ISBN:2-85653-500-3
Résumé [+]
[-]
The Macroramphosid fish Notopogon xenosoma Regan 1914 is recorded on the northern part of the Norfolk ridge and the
southern shelf of New Caledonia from ORSTOM trawl surveys. It becomes the most northernly distribuuon m the south-west
Pacific Ocean for this subtropical species. Other specimens have been identified from Madagascar collections and induces the
same conclusion for the south-west Indian Ocean.
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Faber M.J. 2013. Ten new species of Rissoinidae from the Central Indo-Pacific (Gastropoda: Rissooidea). Miscellanea Malacologica 6(2): 15-34
Résumé [+]
[-]
From the Philippines, Vanuatu, and New Caledonia, ten new species of Rissoinidae are described, namely Ailinzebina laticostata, A. sleursi, Rissoina aspera, R. guttulata, R. limicola, R. maestratii, R. neptis, R. opalia, R. quasimodo, and Takirissoina crocata. The material was obtained by various cruises organized by, or in cooperation with, the Muséum National d’Histoire Naturelle in Paris. The new species are compared with other rissoinids that are already known. Their vertical distribution varies from 2 to 430 m below sea-level.
Campagnes accessibles citées (5) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Fedesov A.E. & Kantor Y.I. 2008. Toxoglossan gastropods of the subfamily Crassispirinae (Turridae) lacking a radula, and a discussion of the status of the subfamily Zemaciinae. Journal of Molluscan Studies 74(1): 27-35. DOI:10.1093/mollus/eym042
Résumé [+]
[-]
Two new species of Horaiclavus, lacking radula, venom gland and proboscis, are described. The genus is placed in the subfamily Crassispirinae (Turridae). Both species possess a peculiar foregut structure, the muscular rhynchodaeal outgrowth situated in the rhynchocoel. The possible function of the rhynchodaeal outgrowth is discussed. Other studied species of Horaiclavus possess a radula of a typical ‘crassispirine’ type but lack the outgrowth. The anatomy of the foregut of the new species is superficially similar to that of Zemacies excelsa (Turridae: Zemaciinae), which also possesses an additional structure of the rhynchocoel, namely the ‘pyriform gland’. Conchologically, there is no resemblance between Zemacies and Horaiclavus and it is concluded that similar foregut arrangement appeared independently in both lineages. A new monotypic subfamily Zemaciinae was erected mostly on the basis of the unique foregut arrangement of Zemacies excelsa. We express doubts concerning the importance of these characters in establishing a new taxon of subfamilial rank and therefore the validity of the subfamily Zemaciinae.
Campagnes accessibles citées (12) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
LAGON,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
NORFOLK 1,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Fehse D. 2017. Contributions to the knowledge of the Triviidae, XXIX -J. New Triviidaefrom the Solomones. Visaya(Suppl. VIII): 65-94
Campagnes accessibles citées (12) [+]
[-]
BERYX 11,
CONCALIS,
EBISCO,
LAGON,
LIFOU 2000,
LITHIST,
MUSORSTOM 6,
NORFOLK 1,
NORFOLK 2,
SALOMON 1,
SALOMON 2,
SALOMONBOA 3
Codes des collections associés:
IM (Mollusques)
-
Fehse D. 2017. Contributions to the knowledge of the Triviidae, XXIX-G. New Triviidae from Tonga Islands. Visaya Suppl. VIII: 5-30
Campagnes accessibles citées (14) [+]
[-]
BENTHAUS,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CONCALIS,
EBISCO,
LIFOU 2000,
LITHIST,
MUSORSTOM 5,
MUSORSTOM 6,
NORFOLK 1,
NORFOLK 2,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Fraussen K., Kantor Y.I. & Hadorn R. 2007. Amiantofusus gen. nov. for Fusus amiantus Dall, 1889 (Mollusca: Gastropoda: Fasciolariidae) with description of a new extensive Indo-West Pacific radiation. Novapex 8(3-4): 79-101
Résumé [+]
[-]
In the present paper we describe the new genus Amiantofusus gen. nov. to accommodate the Atlantic species Fusus amiantus Dall, 1889. The genus belongs to Fasciolariidae and this family is confirmed as distinct from Buccinidae, based on anatomical differences. We add an Indo-West Pacific fauna of seven species described as new to science: miantofusus pacificus sp. nov. (North Fiji Basin, New Caledonia, southern Coral Sea, south West Pacific), A. gloriabundus sp. nov. (North Fiji Basin, Vitiaz Zone), A. sebalis sp. nov. (New Caledonia, Loyalty Islands, Vanuatu), A. candoris sp. nov. (Chesterfield Islands, Fairway), A. maestratii sp. nov. (New Caledonia), A. borbonica sp. nov. (Reunion) and A. cartilago sp. nov. (Mozambique Channel). In addition we add two unnamed species: A. species 1 (North Fiji Basin) and A. species 2 (Vanuatu). Fusus thielei Schepman, 1911 is briefly discussed, the generic placement is still uncertain.
Campagnes accessibles citées (27) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
Restreint,
BIOCAL,
BIOGEOCAL,
BORDAU 2,
CHALCAL 2,
CORAIL 2,
EBISCO,
HALIPRO 1,
MD32 (REUNION),
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
Restreint,
SMIB 3,
SMIB 4,
SMIB 8,
TAIWAN 2000,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Fraussen K. & Stahlschmidt P. 2016. The extensive Indo-Pacific deep-water radiation of Manaria E. A. Smith, 1906 (Gastropoda: Buccinidae) and related genera, with descriptions of 21 new species, in Héros V., Strong E.E. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 29. Mémoires du Muséum national d’Histoire naturelle 208. Muséum national d'Histoire naturelle, Paris:363-456, ISBN:978-2-85653-774-9
Résumé [+]
[-]
The tropical deep-water Cominellinae commonly assigned to the genera Manaria E. A. Smith, 1906 and Eosipho Thiele, 1929 are revised. While the taxonomic details at the generic level were discussed by Kantor et al. (2013), the species level is discussed here. Twentyone new species are described: Manaria astrolabis n. sp. (French Polynesia), M. borbonica n. sp. (Réunion), M. circumsonaxa n. sp. (Papua New Guinea and the Solomons), M. corindoni n. sp. (Indonesia), M. corporosis n. sp. (the Solomons, Vanuatu, Coral Sea and New Caledonia), M. explicibilis n. sp. (Papua New Guinea and the Solomons), M. excalibur n. sp. (Indonesia and Western Australia), M. fluentisona n. sp. (the Solomons, Fiji, Wallis and Tonga), M. hadorni n. sp. (Papua New Guinea and New Caledonia), M. indomaris n. sp. (India), M. loculosa n. sp. (Fiji), M. lozoueti n. sp. (North Fiji Basin), M. terryni n. sp. (Mozambique Channel), M. tongaensis n. sp. (Tonga), M. tyrotarichoides n. sp. (Mozambique Channel), Calagrassor bacciballus n. sp. (Philippines), C. delicatus n. sp. (New Zealand), C. hespericus n. sp. (Mozambique), C. pidginoides n. sp. (Philippines, Papua New Guinea, the Solomons and Vanuatu), Enigmaticolus marshalli n. sp. (Kermadec Ridge, Monowai Caldera), and E. voluptarius n. sp. (New Caledonia). Considerable range extensions are recorded: Manaria kuroharai Azuma, 1960 is recorded from the Solomons, New Caledonia, Vanuatu and Tonga; M. brevicaudata (Schepman, 1911) is recorded from Taiwan, the Philippines, the Solomons and Fiji; and Calagrassor poppei (Fraussen, 2001) is recorded from Indonesia and the Solomons. Lathyrus jonkeri Koperberg, 1931, a fossil described from Indonesia, is recorded from the Recent fauna of Indonesia, Philippines and Fiji and is redescribed and placed in Manaria. Sipho jonkeri Koperberg, 1931, another fossil described from Indonesia in the same work, is a secondary homonym of Manaria jonkeri (Koperberg, 1931) and is renamed Manaria koperbergae nom. nov.
Campagnes accessibles citées (51) [+]
[-]
AURORA 2007,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BIOCAL,
BIOGEOCAL,
Restreint,
BIOPAPUA,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CONCALIS,
CORAIL 2,
CORINDON 2,
Restreint,
Restreint,
Restreint,
EBISCO,
HALIPRO 1,
KARUBAR,
MAINBAZA,
MIRIKY,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
SALOMONBOA 3,
SANTO 2006,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2004,
TARASOC,
TERRASSES,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
García E.F. 2004. On the genus Cycloscala Dall, 1889 (Gastropoda: Epitoniidae) in the Indo-Pacific, with comments on the type species, new records of known species, and the description of three new species. Novapex 5(2-3): 57-68
Résumé [+]
[-]
All described Indo-Pacific taxa referable to the epitoniid genus Cycloscala Dall, 1889 are listed and evaluated. The type species, Cycloscala echinaticosta (d'Orbugny, 1842) is discussed. Four described Inod-Pacific Cycloscala species, considered valid herewith, are treated: Cycloscala crenulata Pease, 1867; C. gazae Kilburn, 1985; C. hyalina Sowerby II, 1844; and C. revoluta Hedley, 1899. Three new species are described: Cycloscala armata, C. sardella, and C. montrouzieri.
Campagnes accessibles citées (15) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOGEOCAL,
BORDAU 2,
LIFOU 2000,
MD32 (REUNION),
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 3,
MUSORSTOM 6,
MUSORSTOM 8,
MUSORSTOM 9,
Restreint
Codes des collections associés:
IM (Mollusques)
-
Geiger D.L. 2012. Monograph of the little slit shells. Volume 1. Introduction, Scissurellidae 1. Santa Barbara Museum of Natural History Monographs 7. Santa Barbara Museum of Natural History, Santa Barbara, CA, 1-728 ISBN:978-0-936494-45-6
Campagnes accessibles citées (23) [+]
[-]
ATIMO VATAE,
AURORA 2007,
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
CONCALIS,
MAINBAZA,
MUSORSTOM 10,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
SMIB 8,
TARASOC
Codes des collections associés:
IM (Mollusques)
-
Geiger D.L. 2012. Monograph of the little slit shells. Volume 2. Anatomidae, Larocheidae, Depressizonidae, Sutilizonidae, Temnocinclidae 2. Santa Barbara Museum of Natural History Monographs 7. Santa Barbara Museum of Natural History, Santa Barbara, CA, 729-1291 ISBN:978-0-936494-45-6
Campagnes accessibles citées (23) [+]
[-]
ATIMO VATAE,
AURORA 2007,
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
CONCALIS,
MAINBAZA,
MUSORSTOM 10,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
SMIB 8,
TARASOC
Codes des collections associés:
IM (Mollusques)
-
Geiger D.L. & Marshall B.A. 2012. New species of Scissurellidae, Anatomidae, and Larocheidae (Mollusca: Gastropoda: Vetigastropoda) from New Zealand and beyond. Zootaxa 3344: 1-33
Résumé [+]
[-]
Thirteen new species of Scissurellidae (Scissurella regalis n. sp., Sinezona mechanica n. sp., Sinezona platyspira n. sp., Sinezona enigmatica n. sp., Sinezona wanganellica n. sp., Satondella azonata n. sp., Satondella bicristata n. sp.), Anatomidae (Anatoma amydra n. sp., Anatoma kopua n. sp., Anatoma megascutula n. sp., Anatoma tangaroa n. sp.), and Larocheidae (Larochea spirata n. sp., Larocheopsis macrostoma n. sp.) are described, all of which occur in New Zealand waters. The greatest geographic source of new taxa is the islands and underwater features off northern New Zealand. The new shell-morphological term "sutsel" is introduced for the area between the SUTure and the SELenizone.
Campagnes accessibles citées (22) [+]
[-]
AURORA 2007,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CONCALIS,
EBISCO,
HALIPRO 2,
MUSORSTOM 7,
NORFOLK 1,
NORFOLK 2,
PANGLAO 2004,
PANGLAO 2005,
SALOMON 1,
SANTO 2006,
SMIB 8,
TARASOC
Codes des collections associés:
IM (Mollusques)
-
Gomon M.F. & Struthers C.D. 2015. Three new species of the Indo-Pacific fish genus Hime (Aulopidae, Aulopiformes), all resembling the type species H. japonica (Günther 1877). Zootaxa 4044(3): 371. DOI:10.11646/zootaxa.4044.3.3
Résumé [+]
[-]
Descriptions of three new species of the aulopid genus Hime from the central and western Pacific and presumably the easternmost Indian Ocean are presented. Hime surrubea sp. nov., confined to the Hawaiian Island region, has been misidentified in species accounts and faunal lists as H. japonica and although resembling it is separable from that species by its shorter caudal peduncle, slightly larger head, larger eye, especially relative to head size, and slightly smaller pectoral and pelvic fins. Hime capitonis sp. nov. is known conclusively only from seamounts off the southern tip of New Caledonia and Vanuatu, and is distinguishable by its distinctively large head (32.3–35.6% SL) and eyes (orbital diameter 10.8–13.0% SL) and relatively few scales between the anus and anal fin origin (7–9). The Indonesian H. caudizoma sp. nov. is so far known from only 8 specimens, acquired in markets in southeastern Lombok and presumably caught nearby in what would be regarded the eastern reaches of the Indian Ocean. The species is recognisable by its dorsal fin of rather uniform moderate height with nearly straight distal margin and 17 rather than 16 rays, none of which is filamentous in either sex, the second penultimate ray rather than anterior rays the longest in males. Like the other two described here, H. caudizoma has among the largest head and eyes of the family. Observations on the dorsal fin form and other features of H. microps Parin & Kotlyar, 1989 are provided based on a large male specimen collected at Rapa Iti, Austral Islands and a re-evaluation of the original description.
Campagnes accessibles citées (6) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Grandperrin R., Baron J., Cillauren E., David G., Kulbicki M., Lehodey P., Thollot P. & Wantiez L. 1994. Travaux realises par le Centre Orstom de Noumea dans le domaine halieutique, in VINGT-CINQUIEME CONFERENCE TECHNIQUE REGIONALE SUR LES PECHES, 14-18 mars 1994, Nouméa, Commission du Pacifique Sud: 1-9
Campagnes accessibles citées (5) [+]
[-]
-
Grandperrin R. & Richer de forges B. 1999. Programme «Monts sous-marins» (1990-2000) Bilan final. IRD, Nouméa, 49 pp.
Résumé [+]
[-]
Le programme «Monts sous-marins» s'est déroulé au centre IRD de Nouméa depuis 1990 sous la direction de René GRANDPERRIN. Ses objectifs étaient l'étude faunistique des pentes récifales externes, des monts sous-marins et du domaine bathyal supérieur (200-1500 m) et l'évaluation de leurs potentialités halieutiques. 32 campagnes représentant un total de 446 jours de mer ont été effectuées. 18 d'entre elles ont été consacrées à l'halieutique, 13 aux études faunistiques et une à des essais de sondeur. 1496 opérations de prélèvement ont été réalisées (445 pour l'halieutique et 1051 pour la faunistique) avec les engins suivants: casier, chalut à crevettes, chalut de fond à poissons, grand chalut de fond à poissons néo-zélandais, chalut à perche, chalut pélagique à poissons, drague épibenthique, drague à roche, drague Waren et palangre de fond. En ce qui concerne l'halieutique, les ressources des pentes externes (100-600 m) ont été étudiées en Nouvelle-Calédonie et à Vanuatu, archipel pour lequel un atlas des pêches est sous presse. Les monts sous-marins agissent comme des dispositifs de concentration de poissons pour les espèces démersales. En Nouvelle-Calédonie, ils abritent une ressource en Beryx splendens qui fit l'objet d'une exploitation commerciale. Une étude scientifique, basée sur Il campagnes, a pennis de déterminer les paramètres biologiques et dynamiques de l'espèce et de modéliser sa distribution en fonction de la profondeur. Pour la première fois, une corrélation liant la croissance d'un poisson de profondeur avec le phénomène ENSO a été établie. Des travaux de génétiques des populations sont en cours sur cette espèce. Par ailleurs, le programme «Monts sous-marins» collabora étroitement avec le programme ZoNéCo d'identification et d'évaluation des ressources marines de la zone économique de Nouvelle-Calédonie. Deux synthèses portant sur les données thonières et sur les poissons profonds furent réalisées. Un halieute participa aux campagnes de bathymétrie mettant en œuvre un sondeur multifaisceaux à bord du N.O. L'Atalante. Cinq campagnes d'exploration des ressources halieutiques profondes furent effectuées à bord du N.O. Alis à l'aide de chaluts et de palangres de fond. Elles mirent en évidence l'existence de certaines ressources jusque là ignorées des pêcheurs. Les collectes de la faune bathyale ont été réalisées dans le cadre d'opérations conjointes IRD et Muséum national d'Histoire naturelle (MNHN). L'analyse des prélèvements a été possible grâce à un réseau de taxonomistes mis en place par l'IRD (Centre de Nouméa et Antenne du MNHN) et le MNHN ; il compte 181 chercheurs appartenant à 92 institutions de 24 nations différentes, ce qui représente un effort de recherche internationale exceptionnel! Les résultats obtenus dans le Pacifique sud-ouest, et notamment en Nouvelle-Calédonie, ont révolutionné la connaissance de la biodiversité des faunes profondes. 20 volumes des Résultats des campagnes MUSORSTOM qui paraissent dans la série des Mémoires du Muséum national d'Histoire naturelle sont déjà parus (environ 10 000 pages) et un autre est sous presse. Ils traitent de plus de 4500 espèces dont plus de 1300 étaient nouvelles pour la science. 126 genres nouveaux ont été créés de même que 7 familles nouvelles. Au sein de cette étude, la Nouvelle-Calédonie apparaît comme particulièrement riche en espèces et d'une très grande originalité puisque sur-les 1619 espèces actuellement publiées, 60,7 % étaient nouvelles pour la science. Des études phylogénétiques ont été réalisées sur certains groupes zoologiques en utilisant soit des techniques de biologie moléculaire (ADN), soit des méthodes de microscopie électronique. Il s'agit des Crustacés, des Echinodermes (Crinoïdes) et des Brachiopodes, parmi lesquels plusieurs formes panchroniques ont été découvertes. L'accessibilité aux faunes de profondeurs au cours du programme «Monts sous-marins» a permis de récolter des organismes qui ont fait l'objet d'analyses par le programme de pharmacologie (Substances Marines d'Intérêt Biologique: SMIB). Deux bases de données sont directement issues des travaux du programme «Monts sous-marins». Elles concernent les données halieutiques et les données faunistiques. Les premières ont été stockées à la Structure de Gestion et de Valorisation Locale (SGVL) du programme ZoNéCo. Les secondes le sont à l'IRD. Pour chacune d'elles, une procédure de création de sites INTERNET est en cours. Le problème majeur rencontré par le programme fut la disponibilité en personnel. En effet, avec une moyenne de 6 personnes, dont un chercheur et un ingénieur d'étude à plein temps, les effectifs ne dépassèrent jamais un total de 9! Le programme disposa en moyenne de 318 kFlan, dont 40 % sur fonds IRD et 60 % sur financements extérieurs. Les financements extérieurs furent de trois types: FIDES section locale du Territoire de Nouvelle-Calédonie, programme ZoNéCo et, dans une moindre mesure, MAE. Le nombre de publications réalisées par les ressortissants du programme a été de 214, dont 139 pour lesquelles le premier auteur est un membre du programme.
Campagnes accessibles citées (40) [+]
[-]
Restreint,
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
CALSUB,
CHALCAL 1,
CHALCAL 2,
GEMINI,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
SMIB 9,
VAUBAN 1978-1979,
VOLSMAR
-
Guinot D., Jamieson B.G.M. & Richer de forges B. 1994. Relationship of Homolidae and Dromiidae: Evidence from Spermatozoal Ultrastructure (Crustacea, Decapoda). Acta Zoologica (Stockholm) 75(3): 255-267
Résumé [+]
[-]
The homolid spermatozoon, as exemplified by Homola sp., Paromola sp. and Paromola petterdi, differs markedly from spermatozoa of crabs of the Heterotremata-Thoracotremata assemblage but agrees with the sperm of dromiids, in the strongly anteroposteriorly depressed acrosome (apomorphy?) and the capitate form of the perforatorium (a major synapomorphy seen nowhere else in the Crustacea). These similarities support inclusion of the Dromiidae and Homolidae in a single grouping, the Podotremata. The homolid perforatorium differs from that of dromiids in the autapomorphic spiked-wheel form of the anterior expansion. Homolid spermatozoa show nuclear arms symplesiomorphic of all investigated crabs (small or questionably sometimes absent in Dromiidae), and corresponding loss of purely microtubylar arms seen in other reptants. Homolid sperm agree with those of dromiids (synapomorphy?), raninids, higher heterotremes and thoracotremes (homoplasies?) but differ from lower heterotremes, in lacking microtubules in the nuclear arms. A posterior median process of the nucleus in homolids, not seen in dromiids, is shared with anomurans and lower heterotremes. No featlires in the ultrastructure of homolid or dromiid sperm have been detected which associate them exclusively with either the Raninidae or the heterotreme and thoracotreme Brachyura.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Guinot D. & Richer de forges B. 1995. Crustacea Decapoda Brachyura : Révision de la famille des Homolidae de Haan, 1839, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 13. Mémoires du Muséum national d'Histoire naturelle 163:283-517, ISBN:2-85653-224-1
Résumé [+]
[-]
Crustacea Decapoda Brachyura : Revision of the family Homolidae de Haan, 1839.
Collections made by scientists from ORSTOM and during French expeditions, resulting from the cooperation of
ORSTOM and the Muséum national d'Histoire naturelle, in the upper bathyal zone of the Indo-West-Pacific (Madagascar,
Seychelles, Indonesia, the Philippines, New Caledonia, Chesterfield Islands, Wallis and Futuna Islands) have accumulated
abundant crustacean material. We have added to it the collections by various Australian, German and Soviet expeditions
in regions poorly explored until now. We have studied also specimens taken by deep traps near atolls in French
Polynesia and in french Anfilles. We have also been able to examine almost all the Homolidae deposited in the large
museums of the world, reference and unidentified collections, and thereby to prepare an account of the Hawaiian,
Japanese, Indian, African, South African and American faunas. From all these collections it has been possible to revise
and restructure the Homolidae world-wide. Examination of all type specimens has been necessary, as has that of all
specimens mentioned in the literature; practically all references and all identifications have been verified.
The Homolidae comprise now 14 genera, studied in terms of their phylogenetic affinities : eight genera already
known (Homola Leach, Paromolopsis Wood-Mason, Paromola Wood-Mason, Latreillopsis Henderson, Homolochunia
Doflein, Hypsophrys Wood-Mason, Homolomannia Ihle, Homologenus A. Milne Edwards) ; two former subgenera
elevated to generic rank (Homolax Alcock, Moloha Bamard) ; and four new genera (Dagnaudus, Ihlopsis, Yaldwynopsis,
Gordonopsis).
Until now quite poor in species, the family now contains in the whole 57 species : it is increased by 17 new species ;
in addition, about ten uncertain species are leaven apart. In the cases of two genera considered amphi-Atiantic, Homola
and Homologenus, a new taxon is described ; Homola minima sp. Nov. Is separated from H. barbata (Fabricius), typically
Mediterranean ; and Homologenus boucheti sp. Nov. Is separated from H. rostratus (A. Milne Edwards), from the American Atlantic. Three other new species are added to Homola : H. eldredgei, H. coriolisi and H. ranunculus. The genus Paromola is confined to some species close to P. cuvieri (Risso) and two new taxa are added : P. bathyalis and P. crosnieri. Six species are attributed to Moloha of which the former is the type species M. alcocki (Stebbing), another one the ancient Latreillopsis major of KUBO (validated) ; it is augmented by two new species, M. alisae and M. grandperrini, and also The genus Latreillopsis receives three new species : L. daviei, L. cornuta and L. antennata. The new genus
Ihlopsis includes, besides I. multispinosa (Ihle) (formely in Latreillopsis), one new species, I. tirardi. A third species, H. gadaletae, is added to Homolochunia. Only one species is added to Hypsophrys, H. futuna, but the genus is certainly
more diverse. Three new species, H. boucheti, H. levii and H. wallis are described in the genus Homologenus. The genus Homolax, poorly known, is well defined.
For each genus adiagnosis, an illustration of the principal characteristics and homologies, plus a key to all species
are given. Each genus has been strictly redefined with respect to its type species and to all its species. For the numerous
poorly known species a description or summary of characters differentiating it from the nearest taxon is presented
H has been made by a synthetic study of all important morphological criteria ; we have reviewed all the principal arrangements and structures of Homolidae to understand their homologies and reach rigorous the nomenclature of the grooves and ornamentation of the carapace which have been often confused in the past. Some phylogenetic hypotheses are briefly presented. The place of the Homolidae in Homoloidea is commented on with a key to the three members of the superfamily. Short remarks, which will be completed in another work, on fossil representatives are outlined.
Lastly, geographic and bathymétrie distribution of the genera and species are discussed.
Each species is represented often with drawings and always by several photographs.
Campagnes accessibles citées (36) [+]
[-]
AZTEQUE,
Restreint,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BENTHEDI,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
Restreint,
HALIPRO 1,
KARUBAR,
LAGON,
MD08 (BENTHOS),
MD32 (REUNION),
MUSORSTOM 1,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
SMCB,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IU (Crustacés)
-
Hadorn R. & Fraussen K. 2003. The deep-water Indo-Pacific radiation of Fusinus (Chryseofusus subgen. nov.) (Gastropoda: Fasciolariidae). Iberus 21(1): 207-240
Résumé [+]
[-]
A number of fusinids from the Indo-Pacific deep-water fauna are studied to get more insight in the distribution and variability. The subgenus Chryseofusus (Gastropoda: Fasciolariidae: Fusinus Rafinesque, 1815) is described as new to accommodate a number of species sharing conchological characteristics different from typical Fusinus. Their separation from Fusinus s.s. is based on differences in axial sculpture (usually absent on body whorl), spiral sculpture (weak, close-set, regular, crossed by distinct growth lines), shape (shorter spire, shorter siphonal canal, less convex whorls with subsutural concavity, less constricted suture) and parietal callus (inner lip smooth, parietal wall covered with an extended, adherent thin layer as callus). Fusinus (Chryseofusus) bradneri (Drivas and Jay, 1990), F. (C.) chrysodomoides (Schepman, 1911), F. (C.) graciliformis (Sowerby, 1880), F. (C.) hyphalus M. Smith, 1940, F. (C.) jurgeni Hadorn and Fraussen, 2002, F. (C.) kazdailisi Fraussen and Hadorn, 2000 and F. (C.) subangulatus (von Martens, 1901) are briefly described and their taxonomic placement in the new subgenus is discussed. To avoid further taxonomic complications, a lectotype is designated for the correct F. (C.) chrysodomoides. F. (C.) acherius (west Madagascar, Mozambique Channel, 1475-1530 m), F. (C.) alisae (north New Caledonia, 444-452 m), F. (C.) artutus (Philippines, Bohol, deep water), F. (C.) cadus (south New Caledonia, 460-470 m), F. (C.) dapsilis (Vietnam, deep water), F. (C.) riscus (New Caledonia, Norfolk Ridge, 394-401 m), F. (C.) scissus (south New Caledonia, 535 m), F. (C.) wareni ( New Caledonia, 480 m), and F. (C.) westralis (northwest Australia, off Port Hedland, 450 m) are described as new to science.
Campagnes accessibles citées (27) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
CORINDON 2,
KARUBAR,
MD32 (REUNION),
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
Restreint,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Hadorn R. & Fraussen K. 2005. Revision of the genus Granulifusus Kuroda & Habe 1954, with description of some new species (Gastropoda : Prosobranchia : Fasciolariidae). Archiv für Molluskenkunde 134(2): 129-171. DOI:10.1127/arch.moll/0003-9284/134/129-171
Résumé [+]
[-]
The genus Granulifusus is distributed over the upper continental shelves in the Indo-West Pacific. The 27 species (21 Recent, 6 fossil) are characterized and separated from Fusinus by a granulated surface sculpture, the Recent also by a small round operculum which does not fill the aperture. Fusus (Sipho) libratus Watson 1886 and Latirus staminatus Garrard 1966 are placed in Granulifusus, their transfer based on the above mentioned conchological characteristics and on radular evidence. Granulifusus niponicus (E.A. Smith 1879), G. kiranus Shuto 1958, G. rubrolineatus (Sowerby II 1870), G. staminatus (Garrard 1966) and G. libratus (Watson 1886) were collected during the Musorstom expeditions and the material is extensively reported on. G. bacciballus sp. nov. (North New Caledonia, 444-452 m), G. benjamini sp. nov. (Coral Sea, Chesterfield, 400 m), G. balbus sp. nov. (South New Caledonia, 470 m), G. amoenus sp. nov. (Vanuatu, 480-544 m), G. geometricus sp. nov. (Tonga Islands, 427-436 m), G. monsecourorum sp. nov. (Madagascar, 240 m) and G. babae sp. nov. (Indonesia, Tanimbar Islands, 206-210 m) were also collected by the Musorstom expeditions and are added to this fauna and described as new species. From the collection of the Australian Museum, Sydney (AMS), one additional Recent species (G. lochi sp. nov., Western Australia, 301-310 m) and one fossil species (G. nakasiensis sp. nov., Nakasi Sandstone Beds, Late Pliocene, Fiji) are described. Lots of the remaining 8 species are studied with the exception of G. captivus (E.A. Smith 1899). The remaining 5 fossil species are listed and compared. G. rufinodis (Von Martens 1901) is tentatively regarded as a distinct species and a lectotype is selected.
Campagnes accessibles citées (32) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORINDON 2,
HALICAL 1,
HALIPRO 2,
KARUBAR,
MUSORSTOM 1,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 8,
SMIB 9,
TAIWAN 2000,
TAIWAN 2001,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Hayashi K.I. 2004. Revision of the Pasiphaea cristata Bate, 1888 species group of Pasiphaea Savigny, 1816, with descriptions of four new species, and referral of P. australis Hanamura, 1989 to Alainopasiphaea Hayashi, 1999 (Crustacea: Decapoda: Pasiphaeidae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:319-373, ISBN:2-85653-557-7
Résumé [+]
[-]
The Pasiphaea cristata species group is treated herewith, as the second part of the revision of genus Pasiphaea Savigny, 1816. The group is primarily characterized by presence of a complete gill formula, unarmed posterior margin of the merus of the first pereopod, and unarmed posterior margin of the ischium and basis of the second pereopod. The group comprises twenty two species, four of which are new species from MUSORSTOM material. Pasiphaea nishiei Iwasaki proves to be a junior synonym of P. merriami Schmitt, and P. vereschhaka Burukovsky is probably a junior synonym of P. amplidens Bate. Pasiphaea australis Hanamura has the same pereopodal armatures as this group, but entirely lacks arthrobranchs and is referred to Alainopasiphaea Hayashi. The genus Pasiphaea is redefined by including Phye Wood-Mason as a synonym. A key to the species of P. cristata group is presented. Each species is defined and most species are redescribed and/or refigured.
Campagnes accessibles citées (17) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
MUSORSTOM 1,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 7,
MUSORSTOM 8,
SMCB
Codes des collections associés:
IU (Crustacés)
-
Ho H.C., Séret B. & Shao K.T. 2011. Records of anglerfishes (Lophiiformes: Lophiidae) from the western South Pacific Ocean, with descriptions of two new species. Journal of Fish Biology 79(7): 1722-1745. DOI:10.1111/j.1095-8649.2011.03106.x
Campagnes accessibles citées (12) [+]
[-]
BERYX 11,
BERYX 2,
BIOCAL,
CHALCAL 2,
LITHIST,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 2,
SALOMON 2
Codes des collections associés:
IC (Ichtyologie)
-
Ho H.C., Roberts C.D. & Stewart A.L. 2013. A review of the anglerfish genus Chaunax (Lophiiformes: Chaunacidae) from New Zealand and adjacent waters, with descriptions of four new species. Zootaxa 3620(1): 89-111. DOI:10.11646/zootaxa.3620.1.4
Résumé [+]
[-]
Species of the anglerfish genus Chaunax Lowe, 1846 from the New Zealand region are taxonomically reviewed with six species recognized and described: Chaunax penicillatus McCulloch; C. nudiventer Ho & Shao, a new record for New Zealand; and four species new to science. Chaunax flavomaculatus sp. nov. distinguished by having its skin covered with a mix of numerous bifurcated and simple spinules, large yellow spots on dorsal surface of fresh specimens, and brownish coloured escal cirri; Chaunax mulleus sp. nov. by having a uniformly pink body with a deep red colour on ventral surfaces of the outer pectoral-fin and pelvic-fin, and lower part of caudal fin; Chaunax reticulatus sp. nov. by having cirri on the dorsal surface of head, and a pale reticulate colour pattern on a greyish background dorsally; and Chaunax russatus sp. nov. by its very wide illicial trough that is usually as wide or wider than the diameter of the pupil, and uniformly deep red
body colour with creamy white to fuzzy greyish spots or patches on its dorsal surface. A key to species recognized from the study area is given.
Campagnes accessibles citées (4) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Ho H.C., Roberts C.D. & Shao K.T. 2013. Revision of batfishes (Lophiiformes: Ogcocephalidae) of New Zealand and adjacent waters, with description of two new species of the genus Malthopsis. Zootaxa 3626(1): 188-200. DOI:10.11646/zootaxa.3626.1.8
Résumé [+]
[-]
Examination and taxonomic review of the batfishes collected from New Zealand and adjacent waters reveals five nominal species: Halieutopsis bathyoreos and Malthopsis mitrigera are recorded from New Zealand for the first time; the synonymy of Halieutaea maoria with H. stellata is confirmed, and two new species are described. Malthopsis asparata sp. nov. is unique in having stout principal bucklers with prominent spines. Malthopsis parva sp. nov. differs from congeners in having a naked abdomen, a short rostral spine directed upward, and all principal bucklers blunt.
Campagnes accessibles citées (2) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Holthuis L.B. 2002. The Indo-Pacific scyllarine lobsters (Crustacea, Decapoda, Scyllaridae). Zoosystema 24(3): 499-683
Résumé [+]
[-]
A revision is provided of the Indo-Pacific species of the subfamily Scyllarinae. All of these species were formerly placed in the genus Scyllarus Fabricius, 1775, but a closer study revealed that several genera could be distinguished within the subfamily. The 13 new genera now recognized in the Indo-Pacific biogeographic region are as follows: Acantharctus n. gen., Antarctus n. gen., Antipodarctus n. gen., Bathyarctus n. gen., Biarctus n. gen., Chelarctus n. gen., Crenarctus n. gen., Eduarctus n. gen., Galearctus n. gen., Gibbularctus n. gen., Petrarctus n. gen., Remiarctus n. gen. and Scammarctus n. gen. Diagnoses and keys are provided for all the genera and their species. New and insufficiently known species have been described extensively, for the others additional morphological details are given. New species are: Bathyarctus chani n. gen., n. sp., B. steatopygus n. gen., n. sp., Petrarctus veliger n. gen., n. sp., Chelarctus crosnieri n. gen., n. sp., Eduarctus pyrrhonotus n. gen., n. sp., E. marginatus n. gen., n. sp., E. perspicillatus n. gen., n. sp. and E. reticulatus n. gen., n. sp. Furthermore efforts were made to provide each species with a complete synonymy, a description of the colour, its biology, habitat and geographical distribution. All the material examined is listed in detail. Where appropriate, remarks are provided on nomenclature, published data on the larval development and other topics.
Campagnes accessibles citées (37) [+]
[-]
Restreint,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BORDAU 1,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
Restreint,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 6,
MUSORSTOM 8,
MUSORSTOM 9,
PALEO-SURPRISE,
Restreint,
Restreint,
SMIB 3,
SMIB 6,
SMIB 8,
Restreint,
Restreint,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Houart R. 2001. Ingensia gen. nov. and eleven new species of Muricidae (Gastropoda) from New Caledonia, Vanuatu, and Wallis and Futuna Islands, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep-Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:243-269, ISBN:2-85653-527-5
Résumé [+]
[-]
Maculotriton ingens Houart, 1987 is transfen'ed from Ergalataxinae to Ingensia gen. novo in Muricinae. Phyllocoma
Tapparone Canefri, 1881 is tentatively assigned to Muricinae, and Pagodula Monterosato, 1884, a hitherto Mediterranean
and eastern Atlantic monotypic genus, is here used to include several Indo-West Pacific, eastern, and western Atlantic
species formerly assigned to Trophonopsis Bucquoy & Dautzenberg, 1882 or to Trophon S. l. Additional records of
previously described and I or recorded species of Pterynotus Swainson, 1833, Actinotrophon Dall, 1902, Leptotrophon
Houart, 1995, and Pagodula Monterosato, 1884 from the New Caledonia region are noted. Eleven new species are
described. Five are representatives of Muricinae: Pterynotus (Pterynotus) rubidus sp. nov., Dermomurex (Trialatella)
triclotae sp. nov., and Ingensia brithys gen. novo and sp. nov., from New Caledonia, Phyllocoma platyca sp. novo from
off Wallis Island, and Poirieria (Actinotrophon) tenuis sp. novo from Vanuatu and off Wallis; one is a muricopsine:
Muricopsis (Murexsul) micra sp. novo from New Caledonia; four are trophonine: Leptotrophon alis sp. nov., L. chlidanos
sp. nov., L. perclarus sp. nov., and Pagodula procera sp. nov., from New Caledonia; one is a rapanine: Thais (Mancinella)
grossa sp. nov., from New Caledonia and Vanuatu.
Campagnes accessibles citées (17) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 2,
HALIPRO 1,
LAGON,
MONTROUZIER,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Houart R. 2012. The Timbellus richeri complex (Gastropoda: Muricidae) in the southwest Pacific. Novapex 13(3-4): 91-101
Résumé [+]
[-]
Two new species of Timbellus are described from the Coral Sea and the New Caledonia region with extension to Fiji, Tonga and the Kermadec Islands for one species. Both species are compared to T. richeri (Houart, 1987) and T. vespertilio (Kuroda, 1959). Nine species of the genus Timbellus are recorded from the Coral Sea and the New Caledonia region. Ouly one, T. bilobatus n. sp. Is known from other localities in the Indo-West Pacific province.
Campagnes accessibles citées (20) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CONCALIS,
EBISCO,
LITHIST,
MUSORSTOM 5,
MUSORSTOM 6,
NORFOLK 1,
NORFOLK 2,
SMIB 2,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (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),
Restreint,
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
Codes des collections associés:
IM (Mollusques)
-
Iwamoto T. & Merrett N.R. 1997. Pisces Gadiformes: Taxonomy of grenadiers of the New Caledonian region, southwest Pacific, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 18. Mémoires du Muséum national d'Histoire naturelle 176:473-570, ISBN:2-85653-511-9
Résumé [+]
[-]
Studies of recent bathyal collections mainly made during MUSORSTOM cruises have shown an extremely diverse
grenadier fauna in the New Caledonian region. A total of 932 grenadier specimens (families Bathygadidae and
Macrouridae) representing 49 species in 16 genera were collected from 102 samples taken from depths between 395 and
2105 m (mid-depth sounding). Of the 49 species, 15 (31%) were found to be new (one recently described) and two are
treated as indeterminate. The collections were dominated by the genera Caelorinchus (14 spp., 5 new), Ventrifossa
(7 spp., 2 new, but one not named), Hymenocephalus (sensu lato) (7 spp., 2 new), and Nezumia (5 spp., 3 new). This
paper reports the taxonomic findings on the collections. A subsequent paper will report on aspects of the distribution
and biology of grenadiers in the New Caledonian region.
Campagnes accessibles citées (15) [+]
[-]
AZTEQUE,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
CHALCAL 2,
CORAIL 2,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
SMIB 1,
SMIB 3,
VOLSMAR
Codes des collections associés:
IC (Ichtyologie)
-
Jamieson B.G.M., Guinot D. & Richer de forges B. 1993. The spermatozoon of Calocarcinus africanus (Heterotremata, Brachyura, Crustacea): ultrastructural synapomorphies With xanthid sperm. Invertebrate Reproduction and Development 24(3): 189-196
Résumé [+]
[-]
Features of the spermatozoon of Calocarcinus apicanus which are general for heterotremes and endorse its inclusion in the Heterotremata are: extension of the subacrosomal chamber almost to the anterior apex of the sperm, presence of an acrosome ray zone, and presence of a thickened ring where the capsule surrounds the base of the subacrosomal chamber. A feature shared with ,highern heterotremes is the restriction of cytoplasm to the periacrosomal region, the arms being nuclear only, in contrast with invasion of their chromatin with cytoplasm and microtubules in majids; and loss of a posterior median process, containing chromatin, which is present in majids as in raninids and homolids. The relationship of Calocarcinus with xanthids is unequivocally apported b y (1) presence of a posterior circumperforatorialz one, the xanthid ring; (2) the precise form of the acrosome ray mne which is wide anteriorly and sends a long acrosome zone; (4) division of the operculum complex into a distinct upper zone and a lower, subopercular zone of lesser diameter; and (5)presence of an accessory ring around the in Calocarcinus may indicate origin of thoracotremes from a related xanthoid stock. A difference of Calocarcinus sperm from those of xanthids is the (plesiomorphic) presence of centrioles, also seen in some heterotremes and thoracotremes. No synapomorphies which are not common to other heterotremes are shared between Calocarcinus and trapeziid sperm. nTrapeziid sperm (plesiomorphically?) lack the xanthid ring, the posterior extension of the acrosome ray zone and the irregular margin of the outer acrosome mne of Calocarcinus and xanthids. Apomorphic features of the Calocarcinus africanus sperm include a spiral Configurationn of the contents of the outer acrosome zone (autapomorphy?), as seen in cross-section, and presence of a periopercular rim. A well developed periopercular rim is known elsewhere only in Potamonautes (family Potamidae), but a rudiment occurs in some xanthids (e.g., Etisus). The periopercular rim is probably a true synapomorphy indicative of relationship of potamids to xanthoids (represented by Calocarcinus) which has been postulated elsewhere on morphological grounds.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Jones D.S. 2000. Crustacea Cirripedia Thoracica: Chionelasmatoidea and Pachylasmatoidea (Balanimorpha) of New Caledonia, Vanuatu and Wallis and Futuna Islands, with a review of all currently assigned taxa, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 21. Mémoires du Muséum national d'Histoire naturelle 184:141-283, ISBN:2-85653-526-7
Résumé [+]
[-]
Balanomorph barnacles of the superfamilies Chionelasmatoidea and Pachylasmatoidea collected by various French deep-sea expeditions in the waters of New Caledonia, Vanuatu, and the Wallis and Futuna Islands are discussed. One sample from the Marianas Islands is also included. Of the 21 species reported herein, 18 are new to science, 2 are recognised as relictual, and 1 represents a northward range extension within the waters of the southwestern Pacific Ocean. In addition 4 new genera and 1 new subfamily are described. An exceptional diversity of species occurs in the subfamilies Pachylasmadnae and Hexelasmadnae of the family Pachylasmatidae. The number of new pachylasmatines described represents 46% of the known species and that of the new hexelasmatines 40%, indicating the richness of these waters. Of the 17 new species described from the waters of New Caledonia, Vanuatu, and the Wallis and Futuna Islands, 14 are considered presently to be endemic to the Vanuatu/New Caledonian region and the remaining 3 occur in a broader area which includes the Futuna and Wallis Islands region. The richest fauna occurs at the Loyalty Islands (15 species), the Norfolk Ridge (11 species) and New Caledonia (11 species). The occurrence of 2 relictual species, the chionelasmaune Chionelasmus darwini and the eolasmatineWaite/aima boucheti, in the waters of the New Caledonian region supports the hypothesis that the southwestern Pacific is a relictual area.
Campagnes accessibles citées (22) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
BIOCAL,
CHALCAL 2,
CORAIL 2,
HALIPRO 2,
LAGON,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Kantor Y.I. & Bouchet P. 1997. The anatomy and systematics of Ceratoxancus, a genus of deep-water Ptychatractinae (Gastropoda: Turbinellidae) with labral spine. The Veliger 40(2): 101-120
Résumé [+]
[-]
The anatomy of Ceratoxancus is characterized by a short or very short proboscis, the presence of an accessory sali vary gland, the ventral odontophoral retractor passing through the nerve ring, and the position of the buccal mass at the proboscis base in contracted condition. These characters are shared by other representatives of the subfamily and confirm the classification of Ceratoxancus in the Ptychatractinae, until now based on shell and radula characters. Ceratoxancus Kuroda, 1952, comprises six species of which four are described as new from the New Caledonia region in deep water (530-830 m). Ceratoxancus elongatus Sakurai, 1958, is removed from the synonymy of C. teramachii Kuroda, 1952, and both species are recorded from the south west Pacific. Species of Ceratoxancus with a long labral spine present numerous shell breakages, while toothless species have mu ch fewer scars, and it is hypothesized that the tooth and outer lip are used in prey capture with accompanying shell breakage.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Kantor Y.I. & Bouchet P. 2007. Out of Australia: Belloliva (Neogastropoda: Olividae) in the Coral Sea and New Caledonia. American Malacological Bulletin 22(1): 27-73. DOI:10.4003/0740-2783-22.1.27
Campagnes accessibles citées (16) [+]
[-]
BATHUS 1,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 1,
CORAIL 2,
EBISCO,
LAGON,
LIFOU 2000,
MONTROUZIER,
MUSORSTOM 4,
MUSORSTOM 5,
NORFOLK 1,
PALEO-SURPRISE,
SMIB 5,
SMIB 8
Codes des collections associés:
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (60) [+]
[-]
ATIMO VATAE,
AURORA 2007,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
CONCALIS,
Restreint,
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,
Restreint
Codes des collections associés:
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
Campagnes accessibles citées (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
Codes des collections associés:
IK (Cnidaires)
-
Komai T. 2004. A review of the Indo-West Pacific species of the genus Glyphocrangon A. Milne-Edwards, 1881 (excluding the G. caeca species group) (Crustacea: Decapoda: Caridea: Glyphocrangonidae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:375-610, ISBN:2-85653-557-7
Résumé [+]
[-]
A review of the species of the caridean genus Glyphocrangon A. Milne-Edwards, 1881 from the Indo-West Pacific Oceans is presented based on rich collections formed during French expeditions to various regions, and supplemented by extensive material deposited in various institutions throughout the world. The genus is divided into two informal groups primarily based on the development of the eye and the presence or absence of arthrobranchs on the first and second pereopods. This study treats species characterized by a well-developed eye and the presence of arthrobranchs on the first and second pereopods (herein called the Glyphocrangon spinicauda species group). A total of 54 species are recognized in the G. spinicauda species group from the Indo-West Pacific region. Of these, the following 28 are new to science: G. albatrossae (Philippines), G. amblytes (Madagascar and South Africa), G. armata (New Caledonia, Vanuatu, Fiji, Wallis and Futuna islands), G. boletifera (Gulf of Aden), G. chacei (Philippines), G. confusa (Indonesia), G. cornuta (New Caledonia), G. crosnieri (Madagascar), G. conodactylus (New Caledonia), G. dimorpha (New Caledonia), G. ferox (Madagascar), G. formosana (Taiwan and East China Sea), G. indonesiensis (Philippines and Indonesia), G. kapala (eastern Australia), G. saintlaurentae (western Indian Ocean), G. major (New Caledonia), G. lineata (Indonesia and northwestern Australia), G. parva (Philippines), G. perplexa (Japan and Taiwan), G. proxima (Philippines and Indonesia), G. punctata (Philippines), G. richeri (Wallis and Futuna islands), G. robusta (Philippines), G. rubricinctuta (Wallis and Futuna islands), G. runcinata (East China Sea), G. similior (Coral Sea), G. speciosa (New Caledonia), and G. tasmanica (Tasman Sea). Glyphocrangon andamanensis Wood-Mason & Alcock, 1891 and G. mabahissae Calman, 1939, which have been considered to be synonymous with G. investigatoris Wood-Mason in Wood-Mason & Alcock, 1891 and G. dentata Barnard, 1926 respectively, are found to be distinct species. Glyphocrangon juxtaculeata Chace, 1984, the holotype of which is a juvenile, is considered to be a junior subjective synonym of G. regalis Bate, 1888. Glyphocrangon joani Allen & Butler, 1994 is treated as a junior synonym of G. fimbriata Komai & Takeuchi, 1994. Plastocrangon Alcock, 1901 is interpreted as a synonym of Glyphocrangon. The new species are fully described and illustrated, and all but three of the previously known species are redescribed and illustrated: G. gilesii and G. smithii being diagnosed on the basis of published information, G. unguiculata Wood-Mason in Wood-Mason & Alcock, 1891 on published information and provisionally identified material from the western Pacific. One obscurely diagnosed species, G. wagini Burukovsky, 1990 from the southeastern Pacific, is also redescribed in order to establish its affinities. Lectotypes are designated for G. acuminata Bate, 1888, G. pugnax de Man, 1918, G. assimilis de Man, 1918, G. sibogae de Man, 1918, and G. megalophthalma de Man, 1918. Identification key, separated by sex, is provided. This study reveals that most Glyphocrangon species have restricted geographical ranges, with only G. caecescens occurring in both the western Pacific and Indian oceans. The geographic and bathymetric distributions of the treated species are summarized.
Campagnes accessibles citées (24) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
Restreint,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
MD28 (SAFARI II),
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8
Codes des collections associés:
IU (Crustacés)
-
Komai T. 2006. Revision of the Glyphocrangon caeca species group (Crustacea, Decapoda, Glyphocrangonidae), in Richer de forges B. & Justine J.L.(Eds), Tropical Deep-Sea Benthos 24. Mémoires du Muséum national d'Histoire naturelle 193:243-264, ISBN:2-85653-585-2
Résumé [+]
[-]
A review of the species of the Glyphocrangon caeca Wood-Mason & Alcock, 1891 group is presented based on samples obtained during French expeditions to the southwestern Pacific and western Indian Ocean, and supplemented with materials deposited in various museums and institutions in the world. Eight species are now recognized in this species group. The two previously described species, G. caeca from the Bay of Bengal and G. cerea Alcock & Anderson, 1894 from the Laccadive Sea, are rediagnosed based on literature, as types or supplemental topotypic specimens of these two species have not been available for study. Six new species are described: G. brevis n. sp. from Madagascar, G. demani n. sp. from Indonesia, G. humilis n. sp. from Japan and Taiwan, G. musorstomia n. sp. from Wallis and Futuna Islands, Vanuatu, Fiji and Chesterfield Islands, G. parviocullus n. sp. from New Caledonia, and G. rudis n. sp. from the Solomon Islands. Species of this group occur exclusively in the Indo-West Pacific. The horizontal and bathymetric distributions of the species are briefly summarized. The available data suggests that species of the group are highly localized.
Campagnes accessibles citées (12) [+]
[-]
BERYX 11,
BIOCAL,
BIOGEOCAL,
HALIPRO 1,
HALIPRO 2,
MUSORSTOM 10,
MUSORSTOM 5,
MUSORSTOM 7,
MUSORSTOM 8,
SALOMON 1,
TAIWAN 2001,
TAIWAN 2002
Codes des collections associés:
IU (Crustacés)
-
Kool H.H. 2004. Nassarius olomea Kay, 1979, revalidated (Gastropoda, Caenogastropoda, Nassariidae). Basteria 68: 21-24
Résumé [+]
[-]
Contrary to data in the literature, Nassarrius alomea Kay, 1979, has a much wider distribution than only the Hawaiian Islands. It occurs also in parts of the southwestern Pacific. Nassarius alamen and N. crebricostatus (Schepman, 1911) are shown to be separate species.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOGEOCAL,
LITHIST,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
PALEO-SURPRISE,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Kool H.H. 2005. Two new western Pacific deep water species of Nassarius (Gastropoda: Prosobranchia: Nassariidae): Nassarius herosae sp. nov. and Nassarius vanpeli sp. nov. Gloria Maris 44(3-4): 46-54
Résumé [+]
[-]
During several expeditions by the Museum National d'Histoire Naturel, Paris, two hereby described deep water species of Nassarius were collected.
Campagnes accessibles citées (19) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
SALOMON 1,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Kosuge S. & Oliverio M. 2001. A new Coralliophiline species from the Southwest Pacific (Neogastropoda : Muricidae : Coralliophilinae). Journal of Conchology 37(3): 285-290
Résumé [+]
[-]
A new coralliophiline species with striking morphological features is described from several stations sampled in deep waters off New Caledonia. It is compared with related species of Babelomurex and Hirtomurex. It is currently known only from a restricted area in the south-west Pacific.
Campagnes accessibles citées (10) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Lamprell K.L. & Healy J.M. 2001. Spondylidae (Bivalvia) from New Caledonian and adjacent waters, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep-Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:111-163, ISBN:2-85653-527-5
Résumé [+]
[-]
Thirty-two species of Spondylus (Spondylidae) including eight previously undescribed, are recorded from material collected
off New Caledonia and adjacent waters. Most of the species live in shallow water in coral reef and lagoonal environments, but
at least four species have their main distribution at depths around 200 m, with one species occurring at 700 m. Spondylus
exiguus sp. novo is the smallest known species in the family, with a maximum size of 6.4 mm. Spondylus flabellum Reeve, 1856
is placed into the synonymy of S. anacanthus Mawe, 1823. Confusion surrounding usage of the names Spondylus anacanthus
and S. sanguineus Dunker, 1852 is finally resolved. The name Spondylus anacanthus, which has previously been applied to
S. occidens Sowerby, 1903, is shown to be a prior and validly proposed name for S. sanguineus. Despite being well figured by
MAWE, the absence of any documented type material for Spondylus anacanthus necessitates the establishment of a neotype for
this species. Lectotypes are designated for Spondylus albibarbatus, S. butleri, S. castus, S. flabellum, S. ocellatus, S. pacificus,
S. plurispinosus, and S. rubicundus, all of Reeve, 1856. By First Reviser action, the name Spondylus nicobaricus Schreibers,
1793 is given precedence over S. pseudochama Schreibers, 1793.
Campagnes accessibles citées (24) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
LAGON,
MONTROUZIER,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
SMIB 10,
SMIB 3,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Last P.R., Séret B. & Pogonosk J.J. 2007. Part 3—Squalus bucephalus sp. nov., a new short-snout spurdog from New Caledonia, in Last P.R., White W.T. & Pogonosk J.J.(Eds), Descriptions of new Dogfishes of the genus Squalus (Squaloidea: Squalidae) 14. Descriptions of new Dogfishes of the genus Squalus (Squaloidea: Squalidae):23-29
Résumé [+]
[-]
A new species of spurdog, Squalus bucephalus sp. nov., is described from deepwater south
of New Caledonia in the northern Tasman Sea. It belongs to the ‘megalops-cubensis group’ but differs from
Australian forms of S. megalops in having a broader head, larger dorsal-fin spines and reaches a larger
adult size. It also differs in several other meristic and morphometric details and is the only Squalus known
to possess both unicuspid and multicuspid denticles in adults. It is morphologically similar to the newly
described S. crassispinus from the eastern Indian Ocean, but differs in having a lower, strongly raked first dorsal fin, more vertebrae, and more slender dorsal-fin spines.
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Lehodey P., Richer de forges B., Nauges C., Grandperrin R. & Rivaton J. 1992. Campagne BERYX 11 de pêche au chalut sur six monts sous-marins du Sud-Est de la Zone Economique de Nouvelle-Calédonie (N.O. "Alis", 13 au 23 octobre 1992). Rapport de missions, Rapports de missions Sciences de la Mer Biologie marine 22, ORSTOM, Nouméa, 96 pp.
Campagnes accessibles citées (1) [+]
[-]
-
Lehodey P. & Grandperrin R. 1994. A STUDY OF THE FISHERY AND BIOLOGY OF BERYX SPLENDENS (ALFONSIN) IN NEW CALEDONIA. SPC Fisheries Newsletter 71: 30-36
Campagnes accessibles citées (2) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Lehodey P. 1994. Les monts sous-marins de Nouvelle-Calédonie et leurs ressources halieutiques. Doctoral, Université française du Pacifique, Nouméa, 415 pp.
Campagnes accessibles citées (2) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Lehodey P. & Grandperrin R. 1996. Age and growth of the alfonsino Beryx splendens over the seamounts off New Caledonia. Marine Biology 125: 249-258
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Lehodey P. & Grandperrin R. 1996. Swath Mapping of the Deep-Bottom Fisheries Seafloor and its Application in New Caledonia. Marine Geophysical Researches 18: 449-458
Campagnes accessibles citées (2) [+]
[-]
-
Lehodey P., Marchal P. & Grandperrin R. 1997. Reproductive biology and ecology of a deep-demersal fish, alfonsino Beryx splendens, over the seamounts off New Caledonia. Marine Biology 128: 17-27
Résumé [+]
[-]
The reproductive biology of the alfonsino Beryx splendens was studied by histological examinations, gonadosomatic index and macroscopic scales of maturation of a large sample of gonads. Alfonsino is a gonochoric species. The size-frequency distribution of the sex ratio was bimodal and considered to be due to size dimorphism. In New Caledonia, the breeding period of this species occurs during the southern summer, with a peak in December to January. The spawning stage is attained at a minimum fork length of 28 cm for females and 33 cm for males. The size at which 50% of the population attain sexual maturity (FL50) is 33.2 cm for females and 34.5 cm for males. Maximum potential fecundity is estimated to lie between 270 000 to 675 000 eggs for ®sh between 34 and 40 cm in fork length. It was possible to differentiate vegetative zones, in which juvenile alfonsino grow until they reach maturity, from reproductive zones (®shing grounds) which are inhabited by mature individuals. The larvae and juveniles could be carried from the reproductive zone to the vegetative zone by currents in an oceanic eddy system.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Lemaitre R. 2004. A review of Strobopagurus Lemaitre, 1989 (Crustacea: decapoda: Paguroidea: Parapaguridae), with description of a new species. Scientia Marina 68(3): 355-372
Résumé [+]
[-]
Species of the parapagurid genus Strobopagurus Lemaitre, 1989 are reviewed based primarily on abundant specimens obtained during French campaigns across the Indo-Pacific region. A new species, S. breviacus, is described. The genus contains two other species, S. gracilipes (A. Milne-Edwards, 1891), the type of the genus, and S. sibogae (de Saint Laurent, 1972). One taxon, Parapagurus kilburni Kensley, 1973, originally described from off eastern Africa, has been found to be a junior synonym of S. sibogae. An updated diagnosis of the genus, and diagnoses and comparative illustrations of all three species, are presented together with a key to aid in their identification. Information on live coloration is provided for S. gracilipes and S. sibogae; live coloration of S. breviacus is not known.
Campagnes accessibles citées (35) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
HALIPRO 1,
LIFOU 2000,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
PALEO-SURPRISE,
SALOMON 1,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2003,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Lemaitre R. 2004. A worldwide review of hermit crab species of the genus Sympagurus Smith, 1883 (Crustacea: Decapoda: Parapaguridae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:85-149, ISBN:2-85653-557-7
Résumé [+]
[-]
A review of species of the genus Sympagurus Smith, 1883 (sensu Lemaitre) from the world oceans is presented. The study is based on the rich collections obtained during French campaigns in the Pacific and Indian Oceans, and on additional material in various museums and research institutions throughout the world. The 17 species recognised in this genus occur most frequently between 500 and 1000 m depth, and range from 80 to 2537 m. Some live in striking symbiosis with anthozoan or zoanthid coelenterates that can produce pseudo-shells. Three new species, S. aurantium, S. chani and S. symmetricus, are fully described and illustrated here. Sympagurus rectichela (Zarenkov 1990), a taxon originally described in Parapagurus Smith, 1879, has been found to be a junior synonym of S. dofleini (Balss, 1912); and S. papposus Lemaitre, 1996 is a junior synonym of S. burkenroadi Thompson, 1943. All previously known Sympagurus species are diagnosed or redescribed and illustrated, and data on habitat, symbiotic associations, and coloration are provided. A key to aid in the identification of all Sympagurus species is presented, and their bathymetric and geographic distributions are summarised. The geographic distribution of 14 species (82.3%) includes the Pacific Ocean, 9 (52.9.%) the Indian Ocean, and 3 (1.8%) the Atlantic Ocean. New Caledonia and adjacent islands have the highest number of Sympagurus species in the world, with 12 species known to occur there.
Campagnes accessibles citées (24) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 2,
CHALCAL 2,
CORAIL 2,
HALIPRO 1,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8,
TAIWAN 2000,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Lemaitre R. 2013. The genus Paragiopagurus Lemaitre, 1996 (Crustacea, Decapoda, Anomura, Paguroidea, Parapaguridae): A worldwide review and summary, with descriptions of five new species, in Ahyong S.T., Chan T.Y., Corbari L. & Ng P.K.(Eds), Tropical Deep-Sea Benthos 27. Mémoires du Muséum national d'Histoire naturelle 204:311-421, ISBN:978-2-85653-692-6
Résumé [+]
[-]
A review of the deep-water hermit crab species of the genus Paragiopagurus Lemaitre, 1996 from the world oceans is presented. The core specimen base for this study has come primarily from the abundant collections of species of this genus obtained during French campaigns over the last four decades, and complemented with numerous specimens from many other deep-sea expeditions and deposited in various museum holdings around the world. Paragiopagurus is one of the most speciose genus among the Parapaguridae Smith, 1882, although it is considered a phylogenetically heterogeneous assemblage and does not appear to have an apomorphy of its own. Bathymetrically, the species range in depth from 36 to 2034 m, although they occur most frequently between 200 and 1000 m. The species utilize as housing, gastropod shells (or rarely scaphopod shells, siliceous sponges, or hollow pieces of wood) that may or may not be colonized by actinians or zoanthids. In this review, 24 species are recognized, of which five are new, P. laperousei n. sp., P. orthotenes n. sp., P. oxychelos n. sp., P. trilineatus n. sp., and P. umbonatus n. sp. The new species are fully described and illustrated. All previously known species of the genus are diagnosed or redescribed, and previously published illustrations of important taxonomic characters assembled and complemented, when useful, with new illustrations. The treatment of each species includes a full synonymy, materials examined (type and non-types), colouration, habitat or type of housing used, distribution, and remarks on taxonomy and morphological affinities. Colour photographs are included for 14 of the species. Parapagurus curvispina de Saint Laurent, 1974, a species tentatively moved after its description to Sympagurus Smith, 1883 and then to Paragiopagurus, is herein transferred with certainty to Oncopagurus
Lemaitre, 1996. Parapagurus spinimanus Balss, 1911, a species that had been incorrectly placed in Paragiopagurus, is herein moved to Sympagurus. Parapagurus sculptochela Zarenkov, 1990, a taxon previously considered a junior synonym of Paragiopagurus boletifer (de Saint Laurent, 1972), is herein resurrected as a valid species of Paragiopagurus. The bathymetric and geographic distributions of Paragiopagurus species are summarized and briefly discussed, including a summary table, graph, and map with generalized distribution patterns.
Campagnes accessibles citées (52) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
EBISCO,
HALICAL 1,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
SALOMON 1,
SALOMON 2,
SANTO 2006,
SMCB,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2003,
TAIWAN 2004,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Lemaitre R. 2014. A worldwide taxonomic and distributional synthesis of the genus Oncopagurus Lemaitre, 1996 (Crustacea: Decapoda: Anomura: Parapaguridae), with descriptions of nine new species. The Raffles Bulletin of Zoology 62: 210–301
Résumé [+]
[-]
A worldwide taxonomic and distributional synthesis of the deep-water hermit crab genus Oncopagurus
Lemaitre, 1996 is presented. This genus, originally defined for 10 species is set apart from other Parapaguridae as well as other Paguroidea, by one synapomorphy: the presence of an upwardly curved epistomial spine. This study is based on a large amount of specimens deposited in major museums and collected during deep-sea sampling across the world oceans since the late 1800s, with the bulk of material coming from French campaigns in the Indo-Pacific, central and south Pacific during the last 40 years. A total of 24 species are recognised in this investigation, nine of which are new and fully described and illustrated. All previously known species are diagnosed or re-described, including figures assembled from recent published accounts or newly illustrated, of the most important morphological features useful for identifi cations. Information for each species includes a synonymy (full or abbreviated if a synonymy has recently been published), material examined (type and non-types), variations when signifi cant, colouration when available, habitat or type of housing used, distribution, and remarks on taxonomy and morphological affinities. Rare colour photographs are included for five species. Species of Oncopagurus range in depth from the Continental Shelf (50 m) to the Continental Rise (2308 m), although they are most commonly found in 50–500 m. Individuals of the majority of species in this genus are minute in size (< 3 mm in shield length), species differ in subtle morphological characters, and often exhibit the same broad morphological variations related to sex and size that has been documented in species of other genera of Parapaguridae. Oncopagurus mironovi Zhadan, 1997, a taxon reported from the Nazca and Sala-y-Gómez Ridges, is considered a junior synonym of the widely distributed O. indicus (Alcock, 1905). The bathymetric and geographic distributions of Oncopagurus species are summarised and briefly discussed, complemented with a summary table, graph, and map with generalised distribution patterns. The scant phylogenetic knowledge of this genus is summarised.
Campagnes accessibles citées (46) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORINDON 2,
EBISCO,
HALIPRO 1,
KARUBAR,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
SALOMON 1,
SALOMON 2,
SANTO 2006,
SMCB,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 8,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
TAIWAN 2003,
TAIWAN 2004,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Li X. & Bruce A.J. 2006. Further Indo-West Pacific palaemonoid shrimps (Crustacea: Decapoda: Palaemonoidea), principally from the New Caledonian region. Journal of Natural History 40(11-12): 611-738. DOI:10.1080/00222930600763627
Résumé [+]
[-]
Based on the material deposited in the Museum national d'Histoire naturelle, Paris, collected from the Indo-West Pacific, principally from the New Caledonian region, the present paper reports 117 palaemonoid shrimp species, which belong, respectively, to Anchistioididae ( one genus, one species), Gnathophyllidae ( one genus, one species), Palaemonidae Palaemoninae ( seven genera, nine species), and Palaemonidae Pontoniinae ( 30 genera, 106 species), including eight new species. The new species are all Pontoniinae: Mesopontonia brevicarpalis sp. nov., Palaemonella komaii sp. nov., Periclimenes crosnieri sp. nov., Periclimenes forgesi sp. nov., Periclimenes loyautensis sp. nov., Periclimenes paralcocki sp. nov., Periclimenes paraleator sp. nov., and Periclimenes pseudalcocki sp. nov. The last six new species are members of the deep-water "Periclimenes alcocki species complex'', which has more than two ( usually four) pairs of dorsolateral telson spines anterior to the posterior telson margin, the cornea is usually reduced, the dactyl of the major second chela is generally flanged and the chela is sometimes covered with small tubercles. The complex is usually found at more than 200m depth in the West Pacific. The species can be distinguished from each other by the armature of ambulatory propod and dactyl, diameter of cornea, rostrum shape and the number of pairs of dorsolateral telson spines. Mesopontonia brevicarpalis sp. nov., from the southeast coast of Africa, is the seventh species of the genus. Palaemonella komaii sp. nov. is very similar to Palaemonella dolichodactylus Bruce, 1991 and Palaemonella hachijo Okuno, 1999. These three species share the features of very long and slender ambulatory pereiopods with the dactyl more than eight times longer than its basal depth and with several long setae on the dorsal dactylar margin.
Campagnes accessibles citées (33) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LIFOU 2000,
LITHIST,
MD32 (REUNION),
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
PALEO-SURPRISE,
Restreint,
SALOMON 1,
SALOMON 2,
SMIB 8,
Restreint,
Restreint
Codes des collections associés:
IU (Crustacés)
-
Lorenz F. 2002. New worldwide Cowries. Descriptions of new taxa and revisions of selected groups of living Cypraeidae (Mollusca: Gastropoda) 19. ConcBooks, Hackenheim, Germany, 292 pp. ISBN:3-925919-59-7
Résumé [+]
[-]
This book describes taxa of cowries, some of which are new to science; others have to date been known only by taxonomically invalid forma-names: valid species: aenigma, colligata, deforgesi. New species by revision and promoting of rank: valid species: aenigma, colligata, deforgesi. New species by revision and lifting of rank: boucheti, gilvella, johnsonorum. New subspecies: caurica samoensis, citrina dauphinensis, coronata debruini, decipiens suprasinum, exmouthensis abrolhoensis, e. magnifica, jeaniana thalamega, katsuae guidoi, maculifera martybealsi, m. scindata, mappa admirabilis, teramachii polyphemus, langfordi cavatoensis, stolida brianoi, subteres violacincta, teres janae, and new subspecies by taxonomic validation: bregeriana pervelata, cinerea brasilensis, connelli peelae, cribraria australiensis, exmouthensis rottnestensis, fimbriata marquesana, fuscodentata grohorum, f sphaerica, mappa aliwalensis, pellucens panamensis, porteri nigromaculata, rosselli latistoma, r. satiata, scurra mundula, teramachii neocaledonica. Taxonomically valid names of other authors are elevated to species rank: exmouthensis, geographica, pellucens, and in some cases, to subspecies rank: cribraria zadela, fuscorubra gondwanalandensis, teres alveolus. Some genera and species-complexes are discussed in detail: the Leporicypraea mappacomplex, some species of the deep-water genus Nesiocypraea, the Western Australian members of Cribrarula, the genus Cypraeovula and its zoogeography, Erronea caurica and its subspecies, and the Blasicrura (Talostolida) teres species-complex. The distributions of all new taxa and related species-complexes are shown. In an illustrated checklist, all species, subspecies and commonly used forma-names of the living Cypraeidae are listed, including the new species and subspecies described herein.
Campagnes accessibles citées (21) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
CHALCAL 2,
LAGON,
LIFOU 2000,
LITHIST,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
SMIB 4,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Lorenz F. & Fehse D. 2009. The living Ovulidae: a manual of the families of allied cowries: Ovulidae, Pediculariidae and Eocypraeidae. ConchBooks, Hackenheim, 651 pp. ISBN:978-3-939767-21-3 3-939767-21-2
Campagnes accessibles citées (29) [+]
[-]
BATHUS 1,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
EBISCO,
KARUBAR,
LAGON,
MD32 (REUNION),
MONTROUZIER,
MUSORSTOM 2,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
Restreint,
Restreint,
SMIB 8,
TAIWAN 2000,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Luque Á.A., Geiger D.L. & Rolán E. 2011. A revision of the genus Satondella Bandel, 1998 (Gastropoda, Scissurellidae). Molluscan Research 31(1): 1-14
Résumé [+]
[-]
This revision of the scissurellid genus Satondella Bandel, 1998 is mainly based on shell characters due to the availability of only a few live collected specimens. There are seven Recent species (two described as new) and one Eocene fossil. Satondella minuta Bandel, 1998, the type species from Indonesia, is redescribed and its range extended to New Caledonia, Solomon and Fiji Islands. Satondella tabulata (Watson, 1886) is only known from type material off Culebra Island (Puerto Rico); lectotype and paralectotypes are here designated, and similar material from the Indo-Pacific is discussed. Satondella brasiliensis (Mattar, 1987) is another W. Atlantic species, ranging from Bermuda to Brazil. Satondella senni (Geiger, 2003) is only known from the E. Pacific (Easter Island) and Satondella danieli Segers, Swinnen & Abreu, 2009 from the NE. Atlantic Ocean (Desertas and Madeira Islands). The two new species are distributed through the E. Indian and W. Pacific oceans (S. cachoi n. sp.) and W. Pacific (S. dantarti n. sp.). The Tongan Eocene fossil S. kondoi (Ladd, 1970) is redescribed and illustrated with SEM images. Satondella brasiliensis and S. cachoi have a typical scissurellid radula, except for uniquely having one cusp on the inner edge of the third lateral. The monophyly of the genus is discussed, since species currently included in Satondella show two clearly different shell patterns but all share the unique chimney-like foramen.
Campagnes accessibles citées (15) [+]
[-]
BATHUS 2,
BATHUS 3,
BENTHEDI,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
CALSUB,
EBISCO,
MUSORSTOM 10,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
SMIB 3,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Macpherson E. 1996. Crustacea Decapoda : New records of species of the genera Munida Leach, 1820 and Paramunida Baba, 1988 (Galatheidae) from the New Caledonia, with the descriptions of three new species, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 15. Mémoires du Muséum national d'Histoire naturelle 168:423-431, ISBN:2-85653-501-1
Campagnes accessibles citées (5) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Macpherson E. 2004. Species of the genus Munida Leach, 1820 and related genera from Fiji and Tonga (Crustacea: Decapoda: Galatheidae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:231-292, ISBN:2-85653-557-7
Campagnes accessibles citées (23) [+]
[-]
BATHUS 1,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 2,
CORAIL 2,
HALIPRO 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SMIB 3,
SMIB 4,
SMIB 8
Codes des collections associés:
IU (Crustacés)
-
Macpherson E., Richer de forges B., Schnabel K., Samadi S., Boisselier M.C. & Garcia-rubies A. 2010. Biogeography of the deep-sea galatheid squat lobsters of the Pacific Ocean. Deep Sea Research Part I: Oceanographic Research Papers 57(2): 228-238. DOI:10.1016/j.dsr.2009.11.002
Résumé [+]
[-]
We analyzed the distribution patterns of the galatheid squat lobsters (Crustacea, Decapoda, Galatheidae) of the Pacific Ocean. We used the presence/absence data of 402 species along the continental slope and continental rise (200-2000 m) obtained from 54 cruises carried out in areas around the Philippines, Indonesia, Solomon, Vanuatu, New Caledonia, Fiji, Tonga, Wallis and Futuna and French Polynesia. The total number of stations was ca. 3200. We also used published data from other expeditions carried out in the Pacific waters, and from an exhaustive search of ca. 600 papers on the taxonomy and biogeography of Pacific species. We studied the existence of biogeographic provinces using multivariate analyses, and present data on latitudinal and longitudinal patterns of species richness, rate of endemism and the relationship between body sizes with the size of the geographic ranges. Latitudinal species richness along the Western and Eastern Pacific exhibited an increase from higher latitudes towards the Equator. Longitudinal species richness decreased considerably from the Western to the Central Pacific. Size frequency distribution for body size was strongly shifted toward small sizes and endemic species were significantly smaller than non-endemics. This study concludes that a clear separation exists between the moderately poor galatheid fauna of the Eastern Pacific and the rich Western and Central Pacific faunas. Our results also show that the highest numbers of squat lobsters are found in the Coral Sea (Solomon-Vanuatu-New Caledonia islands) and Indo-Malay-Philippines archipelago (IMPA). The distribution of endemism along the Pacific Ocean indicates that there are several major centres of diversity, e.g. Coral Sea, IMPA, New Zealand and French Polynesia. The high proportion of endemism in these areas suggests that they have evolved independently. (C) 2009 Elsevier Ltd. All rights reserved.
Campagnes accessibles citées (36) [+]
[-]
AURORA 2007,
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CONCALIS,
CORAIL 2,
EBISCO,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
TERRASSES
Codes des collections associés:
IU (Crustacés)
-
Macpherson E. 2012. New deep-sea squat lobsters of the genus Galathea Fabricius, 1793 (Decapoda, Galatheidae) from Vanuatu and New Caledonia. Zoosystema 34(2): 409-427. DOI:10.5252/z2012n2a13
Résumé [+]
[-]
During two cruises to Vanuatu, MUSORSTOM 8 (September-October 1994) and SANTO 2006 (September-October 2006), numerous specimens of deep-sea galatheids belonging to the genus Galathea Fabricius, 1793 were collected. The specimens were caught at stations at depths between 180 and 702 m. These collections contain five new species (G. barbellata n. sp., G. echinata n. sp., G. profunda n. sp., G. raventosae n. sp. and G. sanctae n. sp.), all of which are also found in other collections obtained by French cruises to New Caledonia. Galathea barbellata n. sp., G. echinata n. sp. and G. profunda n. sp. are closely related to G. robusta Baba, 1990, from Madagascar, G. raventosae n. sp. resembles G. consobrina De Man, 1902, from Indonesia, the Philippines, South China Sea and SW Australia, and G. sanctae n. sp. is very close to G. multilineata Balss, 1913, from Japan, East China Sea, Taiwan and the Philippines.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 3,
BATHUS 4,
BERYX 11,
BOA0,
HALIPRO 1,
MD32 (REUNION),
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 8,
NORFOLK 2,
SANTO 2006,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 8
Codes des collections associés:
IU (Crustacés)
-
Macpherson E., Rodríguez-flores P.C. & Machordom A. 2020. New occurrences of squat lobsters of the genus Eumunida Smith, 1883 (Decapoda, Eumunididae) in New Caledonia, the Solomon Islands and Papua-New Guinea, with the description of a new species. Zootaxa 4786(4): 485-496. DOI:10.11646/zootaxa.4786.4.2
Résumé [+]
[-]
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.
Campagnes accessibles citées (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
Codes des collections associés:
IU (Crustacés)
-
Mah C. 1999. Taxonomy of the South Pacific brisingidan Brisingaster robillardi (Asteroidea) with new ontogenetic and phylogenetic Information. Zoosystema 21(3): 535-546
Résumé [+]
[-]
New material of Brisingaster robillardi de Loriol 1883, including juveniles, allows a more complete description of the species. Papulae, obscured in the holotype and previously unknown for this taxon, are present. Abactinal plate arrangements provide new autapomorphies for the genus Brisingaster. Scanning electronic microscope photographs of pedicellariae are described and compared with those of Novodinia antillensis. The range of B. robillardi is extended to New Caledonia, Western Australia and Amami-o-shima, Japan. Morphological variation is present between material from the Pacific and the Indian Ocean. Novodinia helenae Rowe, 1989 is synonymized with B. robillardi. New phylogenetic evidence also supporrs a new family, the Brisingasteridae, which tentatively includes Brisingaster and Novodinia.
Campagnes accessibles citées (5) [+]
[-]
Codes des collections associés:
IE (Échinodermes)
-
Mah C. 2005. A phylogeny of Iconaster and Glyphodiscus (Echinodermata, Asteroidea, Valvatida, Goniasteridae) with descriptions of four new species. Zoosystema 27(1): 137-161
Résumé [+]
[-]
A phylogenetic analysis of 11 taxa and 31 characters resulted in a single most parsimonious tree that supports monophyly of the goniasterid genera Iconaster and Glyphodiscus. Four new species, Glyphodiscus magnificus n. sp., Glyphodiscus pentagonalis n. sp., Iconaster uchelbeluuensis n. sp., and Iconaster vanuatuensis n. sp., are described and two species are synonymized. At least three species within the genus Iconaster appear to have invaded shallower water from a deeper-water ancestry. Glassy tubercles, similar to those interpreted as photoreceptors in ophiuroids and other goniasterids, are present in the shallow-water Iconaster clade. Glassy tubercles are largely absent in the deeper-water sister and outgroup taxa, suggesting their occurrence is related to photic zone or shallow-water occupation. Biogeographic patterns as presently known suggest that diversification in Iconaster and Glyphodiscus has been restricted to the central and south Pacific regions.
Campagnes accessibles citées (14) [+]
[-]
BATHUS 1,
BATHUS 3,
BERYX 11,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 6,
MUSORSTOM 8,
SMIB 3,
SMIB 5,
SMIB 8
Codes des collections associés:
IE (Échinodermes)
-
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
Campagnes accessibles citées (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
Codes des collections associés:
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (16) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
EXBODI,
HALIPRO 1,
KANACONO,
KANADEEP,
LITHIST,
MUSORSTOM 10,
MUSORSTOM 4,
NORFOLK 1,
Restreint,
SMIB 4
Codes des collections associés:
IE (Échinodermes)
-
Matsuura K. & Tyler J.C. 1997. Tetraodontiform fishes, mostly from deep water, of New Caledonia, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:173-208, ISBN:2-85653-500-3
Campagnes accessibles citées (8) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Mclaughlin P.A. & Forest J. 1997. Crustacea Depapoda: Diacanthurus gen. nov., a new genus of hermit crabs (Paguridae) with both Recent and fossil representation, and the description of two new species, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 18. Mémoires du Muséum national d'Histoire naturelle 176:235-259, ISBN:2-85653-511-9
Résumé [+]
[-]
The new genus, Diacanthurus, is proposed for a group of three Recent and one fossil species formeriy assigned to the
heterogeneous genus Pagurus Fabricius. In addition to the transfer of Pagurus clifdenensis Hyden & Forest (fossil),
P. spinulimanus (Miers), P. rubricatus (Henderson), and P. ophthalmicus (Ortmann), two new species, Diacanthurus
ecphyma sp. nov. from New Caledonia and Western Australia, and D. richeri sp. nov. from New Caledonia are assigned to
this new genus. Expanded diagnoses or descriptions and illustrations of all Recent species are provided.
Campagnes accessibles citées (10) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Mclaughlin P.A. 2000. Crustacea Decapoda: Porcellanopagurus Filhol and Solitariopagurus Türkay (Paguridae), from the New Caledonia area, Vanuatu and the Marquesas: new records, new species, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 21. Mémoires du Muséum national d'Histoire naturelle 184:389-414, ISBN:2-85653-526-7
Résumé [+]
[-]
The very interesting and rather specialized hermit crab genera Porcellanopagurus and Solitariopagurus are represented in collections from the MUSORSTOM cruises to New Caledonia and the Marquesas by four species of the former and three of the latter. Among the species of Porcellanopagurus, three species, P. tridentatus Whitelegge, P. filholi de Saint Laurent & McLaughlin, and P. chiltoni de Saint Laurent & McLaughlin have heretofore been reported only from Australia and New Zealand; P. haptodactylus sp. nov. is a distinctive species, new to science. Solitariopagurus triprobulus Poupin& McLaughlin is reported for the first time beyond the islands of French Polynesia, and the range of S. tuerkayi McLaughlin is extended from the Kai and Tanimbar Island of Indonesia to New Caledonia, Vanuatu and Okinawa. A new species, S. trullirostris sp. nov., is described from New Caledonia and the Marquesas. The similarities and differences of the two new genera are elucidated, and an apparently rare attribute, a terminal anus, common to some species of both is discussed. The new species are fully described and illustrated, while diagnoses and illustrations of principal diagnostic characters are provided for the previously described species. Keys to the Indo- and western Pacific species of Porcellanopagurus and to the genus Solitariopagurus are included.
Campagnes accessibles citées (12) [+]
[-]
BATHUS 1,
BERYX 11,
BIOCAL,
CHALCAL 2,
MONTROUZIER,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 9,
SMIB 2,
SMIB 5,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Mclaughlin P.A. 2004. A review of the hermit crab genus Nematopagurus A. Milne-Edwards and Bouvier, 1892 and the descriptions of five new species (Crustacea: Decapoda: Paguridae), in Marshall B.A. & Richer de forges B.(Eds), Tropical Deep-Sea Benthos 23. Mémoires du Muséum national d'Histoire naturelle 191:151-229, ISBN:2-85653-557-7
Résumé [+]
[-]
The hermit crab genus Nematopagurus, erected by A. Milne-Edwards & Bouvier (1892) for a single Atlantic species, has vastly larger reported representation in the Indo-Pacific region. However, the majority of species have been described on the basis of one or only a few specimens. The Musorstom expeditions to the south central Pacific and Philippine Islands, supplemented by the surveys of the United States Fish Commission steamer Albatross in Hawaiian, Philippine and Japanese waters, have provided not only a substantial amount of new material, but sufficient representation of most described species to permit the evaluation of intraspecific morphological variation. As a result, although five new species have been recognized, three recently described species have proven to be junior synonyms of previously known, but poorly represented, species. Nematopagurus holthuisi McLaughlin & Hogarth and N. pilosus Komai are synonymous with N. gardineri Alcock, while N. shinnyoae Komai is synonymous with N. kosiensis McLaughlin. The range of N. diadema Lewinsohn, reported previously from the Red Sea, the eastern coast of South Africa, and the South China Sea, has been extended to Fiji, while that of N. meiringae McLaughlin, known from eastern South Africa and the South and East China Seas, has been extended to the Philippine Islands. Nematopagurus kosiensis McLaughlin, previously known only from eastern South Africa has been found not only in Japanese waters, but also as far east as the Hawaiian Islands. Species identified by several authors as N. squamichelis Alcock and N. muricatus (Henderson) have been reexamined and correctly reassigned to other taxa. Descriptions and illustrations are presented for all species, together with a key for their recognition.
Campagnes accessibles citées (31) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
HALIPRO 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Mclay C.L. 1999. Crustacea Decapoda: Revision of the Family Dynomenidae, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 20. Mémoires du Muséum national d'Histoire naturelle 180:427-569, ISBN:2-85653-520-3
Résumé [+]
[-]
The Dynomenidae are a group of small, uncommon, primitive crabs, which are often associated with corals. They inhabit depths down to around 500 m, between latitudes 40°N and 40°S. All genera and species are revised and redescribed, and the genus Dynomene Desmarest, 1823 is divided into two additional genera. As a result, there are thirteen known species belonging to five genera: Dynomene Desmarest, 1823 [D. hispida Guérin-Méneville, 1832, D. praedator A. Milne Edwards, 1879, D. pugnatrix de Man, 1889, D. filholi Bouvier, 1894, and D. pilumnoides Alcock, 1900], Hirsutodynomene gen. nov. [H. spinosa (Rathbun, 1911), and H. ursula (Stimpson, li>60)], Metadynomene gen. nov. [Ai. devaneyi (Takeda, 1977), M. tanensis (Yokoya, 1933), and M. crosnieri sp. nov.], Acanlliodromia A. Milne Edwards, 1880 [A. erinacea A. Milne Edwards, 1880, and A. margarita (Alcock, 1899)], and Paradynomene Sakai, 1963 [P. tuberculata Sakai, 1963]. A key is provided to identify these species. In addition nine fossil genera, dating from the Upper Jurassic, are known: Stephanonietopon Bosquet, 1854, Dromiopsis Reuss, 1859, Palaeodromites A. Milne Edwards, 1865, Cyamocarcinus Bittner, 1883, Graptocarcinus Roemer, 1887, Cyclothyreus Remes, 1895, Gemmellarocarcinus Checchia-Rispoli, 1905, Glyptodynomene Van Straelen, 1944, Trachynotocarcinus Wright & Collins, 1972. Some extinct species have also been placed in the genus Dynomene. The definition of the family Dynomenidae given by ALCOCK (1901) is updated and expanded in order to allow fossil species to be more accurately determined. Because of overlap with the Dromiidae, there has been some uncertainty about true family affinities of some fossils. Although these genera are in need of revision, this is not undertaken in this paper. The status oi Dynomene pilumnoides is established as a valid species, D. pugnatrix brevimana Rathbun. 1911 is synonymized with D. pugnatrix de Man, 1889, D. granulobata Dai, Yang & Lan, 1981 is a synonym of D. hispida, while D. sinensis Chen, 1979, D. tenuilobata Dai, Yang & Lan, 1981, and D. huangluensis Dai, Cai & Yang, 1996 are all synonyms of D. praedator. Dynomenids are reported from Australia for the first time in D. pilumnoides, and Hirsutodynomene spinosa. The status of Metadynomene tanensis (Yokoya, 1933) is established as a widespread Pacific species and shown to be part of the fauna of Japan, where it has been confused with D. praedator. Paradynomene tuberculata, previously known from Japan and New Caledonia, is now recorded from the Gulf of Aden, Indian Ocean. P. tuberculata as well as D. praedator and H. spinosa, are reported from Guam. The Atlantic Ocean and the Indo-Pacific share genera of dynomenids but not species. The biogeographic history of dynomenids is interpreted in the liglit of tfieir present distribution and in relation to plate tectonics. Ancestral dynomenids are assumed to have been tethyan crabs and D. filholi and Acanthodromia erinacea, two insular Atlantic species, are shown to be tethyan relicts. By contrast, Hirsutodynomene ursula from the eastem Pacific, seems to be a species of quite recent origin. In redescribing the species particular attention is paid to some new characters: setae, gills, epipods and gill cleaning mechanisms, the subchelate structure of the last pereopods and the male pleopods. This work was undertaken using a scanning electron microscope. Differences in the gross appearance of setae can be used to separate species and there are substantial differences in setal structure at the microscopic level. The standard branchial formula for dynomenids is shown to be nineteen gills plus seven epipods. There is little variation in gill numbers but substantial variation in gill shape between species. Although dynomenid gills are often said to be "transitional" they are arranged as in phyllobranchs but with the epibranchial part divided into varying numbers of lobes which gives them a trichobranch-like appearance. Acanthodromia has gills which are almost identical to the phyllobranchs of the Dromiidae but which retain the "dynomenid notch" on each side which, in cross section, give each gill plate a violin shape. The gill cleaning mechanism in dynomenids is complex, being carried out by no less than eight appendages (long setae on the posterior margin of the scaphognatbite and the seven epipods) as well as stiff setae on the posterior hypobranchial wall of the gill chamber. In eubrachyurans only three appendages (maxillipodal epipods) are used. In dynomenids the last pereopod is very reduced (on average less than one-third the length of the fourth pereopod) and carried in a horizontal position alongside the posterolateral carapace margin above the base of the preceding pereopod. They are not, as it has been commonly described, carried subdorsally. Using a scanning electron microscope it was revealed that this limb is sexually dimorphic: in males the dactyl has the normal shape of a tiny claw, but in females the dactyl is a flattened plate, bearing five to sixteen spines which are opposable to an extension of the propodus. In both males and females the propodal extension is armed with spines but in Hirsutodynomene. Metadynomene and Paradynotnene, females have a significantly larger number of spines, which are armed with tiny teeth. Males of three species have an additional small spine on the outer margin of the dactyl. This is a character, previously only known amongst the Dromiidae, which suggests that the last pereopod of dynomenids may have evolved from a camouflagecarrying limb. This limb appears to be vestigial and it is difficult to know what its function may have been amongst the dynomenid ancestors. However its most likely former role appears to be as a cleaning appendage, but certainly not for carrying pieces of camouflage as it is found amongst the dromiids and homolids. All dynomenids, except Acanthodromia, lack an effective abdominal locking mechanism and both sexes have five pairs of pleopods. The female has vestigial, uniramous first pleopods followed by four pairs of normal biramous pleopods, while the male has the normal first two pairs of pleopods as well as three pairs of rudimentary pleopods on segments three to five. These rudimentary pleopods can be uniramous or bifid. In Metadynomene tatiensis 17% of females were gynandromorphs with small male first pleopods but the remaining pleopods were normal. The diet of dynomenids seems to consist of food obtained by sieving fine sediment or perhaps coral mucus. The bunches of sfiff setae on the inner margins of the cheliped fingers and third maxillipeds are probably used to separate fine organic fragments. Most of their gut contents are unidentifiable soft organic material along with small amounts of chopped chitinous fragments perhaps coming from hydroids or other crustaceans. Dynomenids appear to be deposit feeders. Dynomenids have a broadcast reproductive strategy, with indirect development, laying small eggs (mean diameter = 0.49 mm) which probably produce planktonic larvae. Dynomenid larvae have never been reported in plankton samples. Males are on average 19% larger than females which become sexually mature at 5-8 mm CW for small species, or 9-13 mm CW for large species. Egg numbers increase logarithmically with body size. Given the sister group relationship with homolodromiids (which have very abbreviated development) it is implied that dynomenids and dromiids evolved from ancestors which had large eggs and perhaps a brooding strategy. This conclusion is contrary to accepted wisdom, but it is the most parsimonious answer. Some dromiids have retained the brooding strategy but others have independently evolved a broadcast strategy. The evolution of such a strategy in both these families is probably related to their colonization of the shallow water habitat. Both dynomenids and dromiids are mostly crabs of the continental shelf whereas homolodromiids are crabs of the continental slope. Using morphological characters the phylogenetic relafionships of the Dynomenidae are examined. Both the Dynomenidae and the Dromiidae are monophylefic, sharing significant apomorphies. The resemblance of some dynomenids and dromiids is shown to be the result of convergent evolution within these families. The Homolodromiidae are also monophyletic but are defined almost exclusively by plesiomorphies. Monophyly of the Dromiacea de Haan, 1833 is supported by morphological characters with the Dynomenidae and Dromiidae together being the sister group of the Homolodromiidae. The ancestor of these three families was probably a camouflage carrying crab, using both of the last two pairs of pereopods. A controversial aspect of the sister group relationships of the dromiaceans is the need to assume that in dynomenids the fourth pereopod has reverted to a locomotory role and the fifth pereopod became a cleaning limb. Monophyly of the Podotremata Guinot, 1977 is also supported. This analysis suggests that camouflage-carrying behaviour has evolved independently in the Dromiidae (and probably in the Homolodromiidae) and the Homolidae. Dromiids carry pieces of sponges or ascidians as well as shells, using the last two pairs of pereopods, while homolids carry sponges or anemones, using only the last pair of pereopods. The ancestor of the Dromiacea and Archaeobrachyura was probably an inhabitant of deeper waters and not a camouflage carrying crab.
Campagnes accessibles citées (28) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHEDI,
BERYX 11,
BIOCAL,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
HALICAL 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
MUSORSTOM 9,
SMCB,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Mcmillan P. & Iwamoto T. 2014. Descriptions of four species of grenadier fishes of the genera Hymenocephalus and Hymenogadus (Teleostei, Gadiformes, Macrouridae) from the New Zealand region and Tasman Sea, including two new species of Hymenocephalus. Zootaxa 3856(1): 117-134. DOI:10.11646/zootaxa.3856.1.5
Résumé [+]
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Two new species of Hymenocephalus are described from the New Zealand region and Tasman Sea. Hymenocephalus fuscus
sp. n. has 11–12 pelvic fin rays, is darkly pigmented, with enlarged bony ridges on the dorsal aspects of head, lacks a chin barbel, has few (16–19) gill rakers on inner side of first arch and is similar to other species in the H. aterrimus species group. Hymenocephalus maculicaudus sp. n. has 8 pelvic fin rays, a mid-lateral line of melanophores on body and tail that
extends about a head length posterior to anal fin origin, a short (7–16 % HL) chin barbel and is similar to other species in the H. megalops species group. Hymenocephalus nascens has 12–14 pelvic fin rays, lacks a chin barbel, has a mid-lateral
stripe of silvery (fresh) or brownish (preserved) pigment running along trunk and tail. Hymenogadus gracilis has a serrated (weak, near tip) first dorsal fin spine, 7–9 pelvic fin rays, long (20–30% HL) chin barbel, and one row of enlarged melanophores along lateral mid-line of the tail. Hymenocephalus nascens and Hymenogadus gracilis are recorded for the first time from the New Zealand region. A key to the known New Zealand species of Hymenocephalus and Hymenogadus is provided.
Campagnes accessibles citées (1) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
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Monsecour K. & Monsecour D. 2016. Deep-water Columbellidae (Mollusca: Gastropoda) from New Caledonia, in Héros V., Strong E.E. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 29. Mémoires du Muséum national d’Histoire naturelle 208. Muséum national d'Histoire naturelle, Paris:291-362, ISBN:978-2-85653-774-9
Campagnes accessibles citées (30) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CONCALIS,
EBISCO,
HALIPRO 2,
LAGON,
LIFOU 2000,
LITHIST,
MD32 (REUNION),
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
NORFOLK 1,
NORFOLK 2,
PALEO-SURPRISE,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 8,
TERRASSES,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
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Nielsen J.G. 1997. Deepwater ophidiiform fishes from off New caledonia with six new species, in Séret B.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:51-82, ISBN:2-85653-500-3
Résumé [+]
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During the ORSTOM explorations (1985-92) off New Caledonia 149 specimens of the order Ophidiiformes were caught.
They represent 24 species of which the following are new: Neobythites bimaculatus, N. longiventralis, N. neocaledoniensis,
N. pallidus, N. zonatus and Parasciadonus pauciradiatus. All 24 species are illustrated and a key is provided
Campagnes accessibles citées (9) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
O'hara T.D. 2008. Bioregionalisation of the waters around Lord Howe and Norfolk Islands using brittle stars (Echinodermata: Ophiuroidea). Department of the Environment, Water, Heritage and the Arts
Résumé [+]
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Ophiuroid assemblages were successfully predicted from current museum sample data using presence-only modeling techniques and a multivariate classification on the resulting species occurrence probabilities across the Coral and Tasman Seas (20-37°S, 148-172°E). The classification involves two-stages. The first uses a non-hierarchical clustering technique to reduce the number of data points (map-pixels) to a manageable number that can be analysed in a second stage with a hierarchical classification method. For both steps, the Bray-Curtis similarity statistic is used.
Campagnes accessibles citées (12) [+]
[-]
BATHUS 3,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CHALCAL 2,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
SMIB 1,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
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O'hara T.D. 2008. Bioregioalisation of the waters around Lord Howe and Norfolk Islands using brittle stars (Echinodermata: Ophiuroidea). Department of the Environment, Water, Heritage and the Arts, 55 pp. ISBN:978-0-0642-55462-8
Campagnes accessibles citées (11) [+]
[-]
BATHUS 3,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CHALCAL 2,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 5,
SMIB 1,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
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O'hara T.D., Rowden A.A. & Bax N.J. 2011. A Southern Hemisphere Bathyal Fauna Is Distributed in Latitudinal Bands. Current Biology 21(3): 226-230. DOI:10.1016/j.cub.2011.01.002
Résumé [+]
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The large-scale spatial distribution of seafloor fauna is still poorly understood. In particular, the bathyal zone has been identified as the key depth stratum requiring further macro- ecological research [ 1 ], particularly in the Southern Hemi- sphere [ 2 ]. Here we analyze a large biological data set derived from 295 research expeditions, across an equator- to-pole sector of the Indian, Pacific, and Southern oceans, to show that the bathyal ophiuroid fauna is distributed in three broad latitudinal bands and not primarily differentiated by oceanic basins as previously assumed. Adjacent faunas form transitional ecoclines rather than biogeographical breaks. This pattern is similar to that in shallow water despite the order-of-magnitude reduction in the variability of environmental parameters at bathyal depths. A reliable biogeography is fundamental to establishing a representative network of marine reserves across the world’s oceans [1, 3].
Campagnes accessibles citées (33) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
GEMINI,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SALOMON 1,
SALOMON 2,
SALOMONBOA 3,
SANTO 2006,
SMIB 2,
SMIB 4,
SMIB 5,
Restreint,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
-
Oliverio M. 2008. Coralliophilinae (Neogastropoda: Muricidae) from the southwest Pacific, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:481-585, ISBN:978-2-85653-614-8
Résumé [+]
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This is a regional revision of the Coralliophilinae (Neogastropoda: Muricidae) from the southwest Pacifi c, based on the material collected during recent expeditions to New Caledonia (including the Coral Sea, mainland New Caledonia, and the Loyalty Islands), Vanuatu, Wallis and Futuna, Fiji and Tonga. It is the fi rst revision of a tropical coralliophiline fauna based on large and extensive sampling, and it yielded a total of 97 coralliophiline species, 13 of them new: Coralliophila candidissima n. sp., C. bathus n. sp., C. norfolk n. sp., C. xenophila n. sp., C. cancellarioidea n. sp., Babelomurex natalabies n. sp., B. pallox n. sp., B. depressispiratus n. sp., B. macrocephalus n. sp., Hirtomurex marshalli n. sp., Mipus tonganus n. sp., M. alis n. sp., and M. boucheti n. sp. A lectotype is selected
for Purpura monodonta Blainville, 1832. In addition, this survey resulted in new biogeographical records for 37 species from the southwest Pacifi c fauna. Regional endemicity may be as high as 17.5% (17 out of 97 species). The protoconchs of 47 species are fi gured by SEM. At least 68 species have planktotrophic development, while 10 species are probably lecithotrophic, either with a short pelagic phase or with a totally intracapsular develoment.
Campagnes accessibles citées (36) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
CORAIL 2,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
LIFOU 2000,
LITHIST,
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
PALEO-SURPRISE,
Restreint,
SALOMON 1,
SMIB 10,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
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O’hara T. & Stöhr S. 2006. Deep water Ophiuroidea (Echinodermata) of New Caledonia: Ophiacanthidae and Hemieuryalidae, in Richer de forges B. & Justine J.L.(Eds), Tropical Deep-Sea Benthos 24. Mémoires du Muséum national d'Histoire naturelle 193:33-141, ISBN:2-85653-585-2
Résumé [+]
[-]
Ophiuroids of the families Ophiacanthidae (46 species) and Hemieuryalidae (2 species) are monographed for the region around New
Caledonia in the southwest Pacific Ocean. Ophiohamus nanus n. gen. n. sp. is described in the Ophioplinthacinae. New species are also
described in the following genera: Ophiacantha (O. fuscina n. sp., O. richeri n. sp.), Ophioplinthaca (O. amezianeae n. sp.), Ophiomitrella (O.
mensa n. sp., O. parviglobosa n. sp.), Ophiothamnus (O. biocal n. sp.) and Ophiurothamnus (O. eleaumei n. sp.). The genus Ophiocyclus is
synonymised with Ophiurothamnus, Ophiomelina with Ophiacantha, Toporkovia with Ophiolimna, Ophiomytis with Ophioplinthaca, and
Ophiogyptis with Ophiomoeris. Ophiomelina moniliformis (Koehler, 1904) thus becomes a junior homonym of Ophiacantha moniliformis
Lütken & Mortensen, 1899 and the replacement name Ophiacantha renekoehleri n. nom. is proposed. In addition there are 37 new
species-level synonymies and 19 other new genus-species combinations. A key is provided for all genera and all tropical Indo-West Pacific
species of the Ophiacanthidae. The results show that the biogeographical relationship of the ophiacanthid fauna of New Caledonia is with
the tropical Indo-Pacific. Less than ten percent of the fauna is shared with Southern Australia and fifteen percent with New Zealand. More
broadly, there appears to be a single ophiacanthid fauna at upper to middle slope depths (200-2500 m) across the Indo-West Pacific from
Africa to Hawaii, with limited east-west differentiation. This fauna grades into distinct temperate bathyal faunas near South Africa,
China/Japan and Australia/New Zealand, until there is an almost complete changeover of species by 45° latitude in both hemispheres.
Campagnes accessibles citées (15) [+]
[-]
BATHUS 3,
BERYX 11,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CHALCAL 2,
HALIPRO 2,
MUSORSTOM 1,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
Restreint,
SMIB 1,
SMIB 4,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
-
O’hara T.D. 2007. Seamounts: centres of endemism or species richness for ophiuroids?. Global Ecology and Biogeography 16(6): 720-732. DOI:10.1111/j.1466-8238.2007.00329.x
Campagnes accessibles citées (31) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
GEMINI,
HALIPRO 1,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SALOMON 1,
SALOMON 2,
SALOMONBOA 3,
SANTO 2006,
SMIB 2,
SMIB 4,
SMIB 5,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
-
O’hara T.D. & Tittensor D.P. 2010. Environmental drivers of ophiuroid species richness on seamounts: Ophiuroid seamount species richness. Marine Ecology 31(Suppl. 1): 26-38. DOI:10.1111/j.1439-0485.2010.00373.x
Campagnes accessibles citées (28) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
GEMINI,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
SMIB 2,
SMIB 4,
SMIB 5,
VOLSMAR
Codes des collections associés:
IE (Échinodermes)
-
Paulin C.D. & Roberts C.D. 1997. Review of the morid cods (Teleostei, Paracanthopterygii, Moridae) of New Caledonia, southwest Pacific Ocean, with description of a new species of Gadella, in Séret B.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:17-41, ISBN:2-85653-500-3
Résumé [+]
[-]
Morid cods, family Moridae, of the New Caledonian Exclusive Economic Zone are reviewed based on fresh specimens
obtained during exploratory fishing by ORSTOM and preserved specimens held in research collections in Paris, Nouméa and
Wellington, The following eleven species in six genera are described: Gadella brocca new species, endemic; Gadella norops
Paulin, southern Indian Ocean and southwestern Pacific Ocean; Laemonema filodorsale Okamura, new record, western Pacific;
Laemonema palauense Okamura, western Pacific Ocean; Lepidion inosimae (Günther), new record, western Pacific Ocean;
Mora moro (Risso), new record, northwest Atlantic Ocean, Mediterranean Sea, southern Indian Ocean and South Pacific
Ocean; Physicidus longifilis Weber, new record, Flores Sea and northern Australia; Physicidus luminosus Paulin, new record,,South Pacific Ocean; Physiculus roseus Alcock, new record, Indian Ocean, South China Sea, Phillipines; Physiculus
therosideros Paulin, southwestern Pacific Ocean; Tripterophycis svetovidovi Sazanov & Shcherbachev, new record, warm
temperate South Atlantic, Indian and Pacific Oceans. A key to the species is provided.
Campagnes accessibles citées (9) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Poppe G.T., Tagaro S.P. & Huang S.I. 2023. The Recent Colloniidae. ConcBooks, Harxheim, Germany, 372 pp.
Campagnes accessibles citées (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,
Restreint
Codes des collections associés:
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, 188 pp. ISBN:978-3-948603-36-6
Campagnes accessibles citées (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,
Restreint,
ZhongSha 2015
Codes des collections associés:
IM (Mollusques)
-
Poutiers J.M. 2006. Two new species of protocardiine cockles (Mollusca, Bivalvia, Cardiidae) from the tropical Southwest Pacific. Zoosystema 28(3): 635-654
Résumé [+]
[-]
The two new species described in this paper are widely distributed in the tropical south-western Pacific; they have been found on the upper continental shelf of the area, around New Caledonia, westward to Chesterfield Islands and Lord Howe Ridge, southward to northern part of Norfolk Ridge, north- and eastward to Vanuatu, Fiji and Tonga islands. They belong to two often confused genera of subfamily Protocardiinae (sensu Keen 1980), Frigidocardium Habe, 1951 and Microcardium Th iele, 1934, that are briefly characterized herein. Frigidocardium valdentatum n. sp. is characterized by the peculiar sculpture of mid-posterior slope ending in strongly dentate margin. Frigidocardium kirana is a similar species with lower outer sculpture, more asymmetrical shape and rather strong umbonoventral fold; it is first recorded here from the tropical Southwest Pacific and Mascarene islands. Diagnostic features of Microcardium trapezoidale n. sp. include rather high trapezoidal shape and posterior sculptural area extending on 2/5 of shell length, with an anterior limit almost parallel to radial ribs in the adult and well-developed, non lamellous sculpture in the rib interstices. A comparative review of all Recent Microcardium species in the Indo-West Pacific is given, to place the new species in the context of the genus. Five Microcardium species are presently known in this area: M. gilchristi from southern Africa, M. simillimum n. comb. (for Cardium (Fragum) simillimum) from Sri Lanka and Mascarene Plateau, M. sakuraii from Japan and the Philippines (new record), M. aequiliratum from the Philippines, and M. tenuilamellosum from the Philippines and Solomon Islands (new record).
Campagnes accessibles citées (22) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CORAIL 2,
HALIPRO 1,
LAGON,
LIFOU 2000,
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
NORFOLK 1,
SMIB 2,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Richer de forges B. 1995. NOUVELLES RÉCOLTES ET NOUVELLES ESPÈCES DE MAJIDAE DE PROFONDEUR DU GENRE OXYPLEURODON MIERS, 1886. Crustaceana 68(1): 43-60
Campagnes accessibles citées (7) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Richer de forges B. & Laboute P. 1996. Langoustes, langoustines et cigales de mer de Nouvelle-Calédonie, in Richer de forges B.(Ed.), Les fonds meubles des lagons de Nouvelle-Calédonie (Sédimentologie, benthos). 2. Etudes et thèses:45-82
Résumé [+]
[-]
This work is a summary of what is known on lobster living in New Caledonia. After general informations about the biology and taxonomy, with keys, each species is described. Several large species of lobsters are mentionned for the first time in New Caledonia : Palinurellus wieneckii, Palinustus unicornutus, Puerulus angulatus, Linuparus sordidus, Justitia chani, J. japonica, Ibacus brucei, Thaumastocheles japonicus. A bibliographic analysis of the Indo-Pacific lobster fisheries, compare the New Caledonia to other Pacific island countries.
Campagnes accessibles citées (4) [+]
[-]
Codes des collections associés:
IU (Crustacés)
-
Richer de forges B. 1998. La diversité du benthos marin de Nouvelle-Calédonie : de l'espèce à la notion de patrimoine. Doctoral, Muséum national d'Histoire naturelle - Paris Ecole Doctorale Sciences de la Nature et de l'Homme, Paris, 327 pp.
Campagnes accessibles citées (37) [+]
[-]
AZTEQUE,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
BIOCAL,
BIOGEOCAL,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
CORINDON 2,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
SMIB 9,
VOLSMAR
-
Roberts C.D. & Paulin C.D. 1997. First record of the Eucla cod, Euclichtys polynemus McCulloch (Teleostei, Paracanthopterygii, Euclichthyidae) from New Caledonia, southwest Pacific Ocean, with notes on morphological characters, in Séret B.(Ed.), Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:43-50, ISBN:2-85653-500-3
Résumé [+]
[-]
The Australasian Eucla cod, Euclichthys polynemus McCulloch, family Euclichthyidae, is described for the first time from
the New Caledonian Exclusive Economic Zone where it appears to be restricted to seamount "B" (24°55'S, 168°21 'E) on the
northern Norfolk Ridge southeast of New Caledonia. The Eucla cod is superficially very similar to morid cods (family Moridae), but can be distinguished by a long filamentous pelvic fin with four to six distal elements, an unequally divided anal fin, and an asymmetrical caudal fin.
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Roberts C.D. & Stewart A.L. 1997. Gemfishes (Scombroidei, Gempylidae, Rexea) of New Caledonia, southwest Pacific Ocean, with description of a new species, Résultats des campagnes MUSORSTOM 17. Mémoires du Muséum national d'Histoire naturelle 174:125-141, ISBN:2-85653-500-3
Résumé [+]
[-]
Gemfishes of the genus Rexea from the New Caledonia Exclusive Economic Zone (EEZ) are reviewed based on fresh and
preserved specimens. Three species are recognized: Rexea aniefurcata Parin, 1989, confirming recent records (previously also
recorded as R. prometheoides), distinguished by the presence of small scales on the caudal peduncle and extending anteriorly
along the edges of the lower lateral line, lateral line branching below the 4th-5th dorsal fm spines, a long pectoral fm, and dusky
colour of spinous dorsal fm membrane and (in adults) pectoral fm; R. bengalensis (Alcock, 1894), first record, distinguished by
its small maximum size, lateral line branching below the 5th-6th dorsal fin spines, long pectoral fin, and naked body (except
lateral line); and R. alisae sp. nov., endemic, distinguished by 3-4 dorsal finlets and 4 anal finlets, lateral line branching below
the 6th to 7th dorsal fin spines, posterior extent of the upper lateral line, its naked body (except lateral line), and coloration. A
key to New Caledonian gemfishes {Rexea spp., Rexichthys johnpaxtoni and Promethichthys prometheus) is provided.
Campagnes accessibles citées (5) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (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
Codes des collections associés:
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
Résumé [+]
[-]
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.
Campagnes accessibles citées (34) [+]
[-]
BATHUS 3,
BERYX 11,
BIOGEOCAL,
BIOMAGLO,
BIOPAPUA,
BOA1,
BORDAU 2,
CHALCAL 2,
Restreint,
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,
Restreint,
TARASOC,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Rubio F. & Rolán E. 2020. Conradiidae Golikov & Starobogatov, 1987 (= Crosseolidae Hickman, 2013) (Gastropoda, Trochoidea) from the Indo-Pacific. III. The genera Conradia and Conjectura. Novapex 21(2-3): 49-91
Résumé [+]
[-]
This is the third contribution to the Indo-Pacific species of the family Conradiidae. In the present work 29 species of the genus Conradia A. Adams, 1860 and one species of the genus Conjectura Finlay, 1927 are studied, 20 of which are considered as new to science, and are described and figured. All these species are compared with the previously known species of these genera. The type material of Conradia carinifera A. Adams, 1860, Conradia cingulifera A. Adams, 1860, Conradia clathrata A. Adams, 1860, Conradia pulchella A. Adams, 1861, Conradia doliaris A. Adams, 1863, Conradia tornata A. Adams, 1863, Conradia (Gottoina) sulcifera A. Adams, 1863 and Conradia (Gottoina) pyrgula A. Adams, 1863 is illustrated for the first time.
Campagnes accessibles citées (15) [+]
[-]
BATHUS 1,
BATHUS 2,
BENTHEDI,
BERYX 11,
BOA0,
BORDAU 1,
EBISCO,
MADEEP,
MUSORSTOM 10,
MUSORSTOM 3,
MUSORSTOM 8,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Röckel D., Richard G. & Moolenbeek R.G. 1995. Deep-water cones (Gastropoda: Conidae) from the New Caledonia region, Résultats des campagnes MUSORSTOM 14. Mémoires du Muséum national d'Histoire naturelle 167:557-594, ISBN:2-85653-217-9
Résumé [+]
[-]
The New Caledonian species of Cones with a main distribution below 100 m are surveyed. This fauna consists of 39 species, of which 5 are new and 18 represent significant range extensions. In addition, eight species, mostly represented by single specimens, remain unidentified. Ten species (Conus boucheti, C. kanakinus, C. luciae, C. plinthis, C. richeri, and the five new ones) are so far only known from the New Caledonia region and may be endemic. Conus smirna and C. profundorum are regarded as distinct, and two additional species are described in this species complex: C. vaubani sp. Nov., from South of New Caledonia and of the New Hebrides Arc in 440-775 m; and C. loyahiensis sp. Nov. From the Loyalty Islands in 480-575 m.
Three other new species, and one subspecies, are named: Conus alisi sp. Nov. From the New Caledonia area, in 200-525 m; C. estivali sp. Nov. From the Chesterfield Islands, Coral Sea, in 355-410 m; C. gondwanensis sp. Nov. From the Norfolk Ridge, South New Caledonia, in 170-260 m; and C. orbignyi coriolisi ssp. Nov., from the Coral Sea, New Caledonia and Loyalty Islands, in 225-550 m.
Campagnes accessibles citées (21) [+]
[-]
BERYX 11,
BIOCAL,
BIOGEOCAL,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
GEMINI,
LAGON,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Saito T. & Komai T. 2008. A review of species of the genera Spongicola de Haan, 1844 and Paraspongicola de Saint Laurent & Cleva, 1981 (Crustacea, Decapoda, Stenopodidea, Spongicolidae). Zoosystema 30(1): 87-147
Résumé [+]
[-]
A review of species of the deep-sea sponge-associated shrimp genera Spongicola de Haan, 1844 and Paraspongicola de Saint Laurent & Cleva, 1981 (Decapoda, Stenopodidea) is presented on the basis of rich collections made by French expeditions in the Indo-West Pacific, supplemented by collections preserved in various institutions in the world. Seven species are recognized in Spongicola, of which three are new to science: S. venustus de Haan, 1844, S. andamanicus Alcock, 1901, S. levigatus Hayashi & Ogawa, 1987, S. parvispinus Zarenkov, 1990, S. depressus n. sp. from Loyalty Islands, S. goyi n. sp. from Japan, Indonesia, New Caledonia and Vanuatu, and S. robustus n. sp. from Mauritius and Mozambique. Subspecific division of S. andamanicus Alcock, 190 1, proposed by de Saint Laurenr & Cleva (198 1), is abandoned, since our morphological analysis strongly suggests that the division does not reflect a population structure of the species; S. holthuisi de Saint Laurent & Cleva, 198 1, is also reduced to a junior synonym of S. andamanicus. Two species are recognized in Paraspongicola, both previously described, viz. P. pusillus de Saint Laurent & Cleva, 1981 and P. inflatus (de saint Laurent & Cleva, 198 1) n. comb., of which the latter is here transferred from Spongicola. Keys in aid for identification are provided for each genus. Geographic and bathymetric distributions of species are briefly discussed. Association with host sponges was verified for some species.
Campagnes accessibles citées (27) [+]
[-]
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 2,
EBISCO,
HALIPRO 2,
KARUBAR,
LIFOU 2000,
LITHIST,
MUSORSTOM 1,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
NORFOLK 2,
SMIB 1,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IU (Crustacés)
-
Salisbury R. & Guillot de suduiraut E. 2003. Three new deep-water miters (Gastropoda: Prosobranchia: Mitridae) from the Western Indo-Pacific with a new name for Mitra millepunctata Schepman, 1911. Novapex 4(1): 1-9
Résumé [+]
[-]
Domiporta dianneae n. sp. Is described from the Indo-Pacific and compared to Domiporta sigillata (Azuma, 1965). Scabricola splendidula n. sp., from the Philippines and Solomon Islands is compared to Scabricola coriacea (Reeve, 1845), Neocancilla clathnis clathrus (Gmelin, 1791) and Neocancilla maciilosa (Gmelin, 1791). Mitra {Mitra) heinickei n. sp. From the Philippine Islands is compared to Mitra {Mitra) maui Kay, 1979 and Ziba? Rehderi (J. H. Webb, 1958). A new record and range for Mitra (Mitra) maui Kay, 1979 is reported. Mitra (Mitra) millepunctata Schepman, 1911 (non Mitra millepunctata Sowerby, 1889) is given a new name: Mitra (Mitra) schepmani.
Campagnes accessibles citées (14) [+]
[-]
BATHUS 2,
BATHUS 3,
BERYX 11,
BIOCAL,
BORDAU 1,
CHALCAL 2,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 5,
SMIB 8,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Scarabino V. 2008. New species and new records of scaphopods from New Caledonia, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:215-268, ISBN:978-2-85653-614-8
Résumé [+]
[-]
Previous work that recorded 75 species of Scaphopoda in New Caledonian waters is augmented with study of new material from several expeditions. The number of species in the region is increased to 115. Of the 40 additional taxa, 28 are described as new, 7 are new records and 5 remain unidentifi ed. Material from New Caledonia previously identifi ed as Antalis phaneum (Dall, 1895) is now determined as A. albatrossae n. sp.; material previously identifi ed as Compressidentalium sedecimcostatum (Boissevain, 1906) is now determined as C. clathratum (Martens, 1881); Episiphon virgula (Hedley, 1903), formerly treated as a synonym of Dentalium subrectum Jeffreys, 1883, is revalidated; material previously identifi ed as Entalina mirifi ca (Smith, 1895) is now determined as E.
dorsicostata Lamprell & Healy, 1998; Fissidentalium transversostriatum (Boissevain, 1906), previously synonymized with F. shoplandi (Jousseaume, 1894), is revalidated and the material previously reported from New Caledonia as the latter in fact belongs to the former. New synonyms: Episiphon jamiesoni Lamprell & Healy, 1998 is synonymized with Gadilina insolita (Smith, 1894); Dentalium
subrectum Jeffreys, 1883 and D. bisinuatum André, 1896 are synonymized with Laevidentalium eburneum (Linné, 1767); Laevidentalium
arnoldi Lamprell & Healy, 1998 is synonymized with L. houbricki Scarabino, 1995; Bathoxiphus steineri Lamprell & Healy, 1998
and B. stanisici Lamprell & Healy, 1998 are synonymized with Solenoxiphus striatulus Chistikov, 1983. New records from the New
Caledonian region: Striodentalium thetidis (Hedley, 1903), Fissidentalium waterhousae Lamprell & Healy, 1998, Calliodentalium
crocinum (Dall, 1907), Gadilina pachypleura (Boissevain, 1906), Laevidentalium eburneum (Linné, 1767), Laevidentalium (?) sominium
Okutani, 1964, Megaentalina mediocarinata (Boissevain, 1906).
Campagnes accessibles citées (22) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
BIOCAL,
BORDAU 2,
HALIPRO 1,
KARUBAR,
LAGON,
LIFOU 2000,
MONTROUZIER,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
PALEO-SURPRISE,
Restreint,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Simone L.R.L. & Cunha C.M. 2008. Supplementary data for a recent revision of the genus Spinosipella (Bivalvia, Septibranchia). Strombus 15(1): 8-14
Résumé [+]
[-]
A supplementary list of material examined is provided, completing the list given in a recently published paper revising the genus Spinosipella worldwide (Simone & Cunha, 2008). Most of the material belongs to the Muséum National d’Histoire Naturelle, Paris, France.
Campagnes accessibles citées (27) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
HALIPRO 1,
HALIPRO 2,
LITHIST,
MUSORSTOM 10,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
NORFOLK 1,
PANGLAO 2005,
SALOMON 1,
SMIB 3,
SMIB 4,
SMIB 8,
Restreint,
TAIWAN 2000,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Sirenko B.I. 2008. Bathyal chitons (Mollusca, Polyplacophora) from off New Caledonia and Vanuatu: families Callochitonidae, Ischnochitonidae and Loricidae, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep-Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:41-75, ISBN:978-2-85653-614-8
Résumé [+]
[-]
Study of deep-water chitons from around New Caledonia and Vanuatu has revealed 35 species, of which 25 species were identified to species and 10 only to genus. This article includes 7 new records for this area of which 4 are described as new species: Ischnochiton crassus Kaas, 1985, Stenosemus robustus Kaas, 1991, S. herosae n. sp., Connexochiton discernibilis Kaas, 1991, Loricella
vanbellei n. sp., L. eernissei n. sp. and L. dellangeloi n. sp. In addition, Vermichiton vermiculus Kaas, 1991 is reviewed. Based on available biogeographic data it is proposed that Loricella originated off South Australia during the Oligocene, in a time of global cooling.
Later, Loricella extended its range north up to Taiwan and east to Tonga, most likely remaining in the bathyal zone. These new discoveries add to the already high diversity and high proportion of endemics known from this region, and a speculative interpretation of these patterns is offered in conclusion.
Campagnes accessibles citées (15) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CALSUB,
CHALCAL 2,
LITHIST,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 8,
NORFOLK 1,
SMIB 3,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Stock J.H. 1997. Pycnogonida collected in recent years around New Caledonia and Vanuatu, in Crosnier A.(Ed.), Résultats des campagnes MUSORSTOM 18. Mémoires du Muséum national d'Histoire naturelle 176:389-409, ISBN:2-85653-511-9
Campagnes accessibles citées (12) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
KARUBAR,
MONTROUZIER,
MUSORSTOM 5,
MUSORSTOM 8,
SMIB 4,
SMIB 8
Codes des collections associés:
IU (Crustacés)
-
Stöhr S. & O'hara T.D. 2003. Deep-sea ophiuroids of New Caledonia - a preliminary report, in Féral J.P. & David B.(Eds), Echinoderm research 2001: proceedings of the sixth European Conference on Echinoderm Research, Banyuls-sur-Mer, France, 3-7 September 2001. Swets & Zeitlinger, Lisse ; Exton, PA:49-52, ISBN:978-90-5809-528-2
Résumé [+]
[-]
A short preliminary report ofan ongoing study of the New Caledonian deep-sea ophiuroid fatma
is presented with a list of39 genera of79 species, including six previously undescribed species and a new gel1lls.
Three species (Astrogynmotes hamishia Baker et al. , 2001, Astrothamnus sp., Ophioli/J/na antarctica (Lyman,
1879)) representing the main groups Ophiomyxidae, Euryalida, and Ophiacanthidae are presented briefly, illustrated
with scanning electron micrographs, as examples of the Im·ger work that will be published elsewhere after
the project will be finished.
Campagnes accessibles citées (14) [+]
[-]
BATHUS 1,
BATHUS 3,
BERYX 11,
BIOCAL,
CHALCAL 1,
CHALCAL 2,
HALIPRO 1,
KARUBAR,
MUSORSTOM 1,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 8,
SMIB 4
Codes des collections associés:
IE (Échinodermes)
-
Sysoev A.V. & Bouchet P. 2001. New and uncommon turriform gastropods (Gastropoda:Conoidea) from the South-West Pacific, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep-Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:271-320, ISBN:2-85653-527-5
Résumé [+]
[-]
Several hundred species of turriform gastropods (Drilliidae, Turridae, Conidae) have been collected at bathyal depths in New Caledonia and other South-West Pacific archipelagoes. Seventeen new species are here described in the genera Drillia (Drilliidae), Inquisitor, Funa, Zemacies, Comitas (Turridae), Benthofascis, Bathytomq Glyphostoma, Daphnella, Spergo, Gymnobela, Teretiopsis, and Rocroithys gen. Novo (Conidae). The genus Zemacies, until now known from Paleocene to Pliocene deposits in New Zealand and Australia, is recognized for the first time in the Recent fauna, and includes Z. excelsa sp. Novo from New Caledonia, and Z. queenslandica (Powell, 1969) comb. nov., from Queensland to Papua. Benthofascis lozoueti sp. Nov., from the Norfolk Ridge, is the second confirmed species of the genus. Bathytoma boholica Parth, 1994 is synonymized with B. atractoides (Watson, 1881), and the validity of B. hedlandensis Tippett & Kosuge, 1994 is questioned. The range of Spergo fusiformis (Kuroda & Habe, 1961), hitherto known only from Japan, is shown to extend to Madagascar and the South-West Pacific. Daphnella itonis, which has been known under that name in the Japanese literature for more than 40 years, is formally described for the first time, based on specimens from New Caledonia. The species has very long radular teeth and, like molluscivorous species of cones, appears to be feeding on gastropods.
Campagnes accessibles citées (33) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
CHALCAL 2,
Restreint,
Restreint,
HALICAL 1,
HALIPRO 1,
KARUBAR,
LAGON,
MUSORSTOM 1,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Séret B., Grandperrin R. & Rivaton J. 1997. Poissons de profondeur et ressources halieutiques de la zone économique de la Nouvelle-Calédonie. Cybium 21(1 suppl.): 99-106
Campagnes accessibles citées (14) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BERYX 2,
CHALCAL 1,
CHALCAL 2,
HALICAL 1,
HALIPRO 1,
HALIPRO 2,
MUSORSTOM 4,
MUSORSTOM 6,
MUSORSTOM 8
Codes des collections associés:
IC (Ichtyologie)
-
Séret B. & Last P.R. 2008. Asymbolus galacticus sp. nov., a new species of spotted catshark (Carcharhiniformes: Scyliorhinidae) from New Caledonia. Cybium 32(2): 137–143
Résumé [+]
[-]
A new species of catshark of the genus Asymbolus is described from 19 specimens collected on seamounts
off southern New Caledonia. It is clearly distinguished from all other Asymbolus species by a striking, variegated colour pattern, comprised of numerous milky white blotches surrounded by rusty-brown spots and blotches, faint dusky dorsal saddles on a light brown dorsal ground colour.
Campagnes accessibles citées (3) [+]
[-]
Codes des collections associés:
IC (Ichtyologie)
-
Tenerio M.J. 2015. Notes on Profundiconus smirna (Bartsch & Rehder, 1943) with description of a new species: Profundiconus smirnoides sp. nov. (Gastropoda, Conilithidae). Xenophora Taxonomy 7: 3-15
Campagnes accessibles citées (13) [+]
[-]
BATHUS 3,
BERYX 11,
CALSUB,
CHALCAL 2,
EBISCO,
LITHIST,
MUSORSTOM 4,
NORFOLK 1,
NORFOLK 2,
SMIB 3,
SMIB 4,
SMIB 8,
TERRASSES
Codes des collections associés:
IM (Mollusques)
-
Valdés Á. 2001. Deep-water phyllidiid nudibranchs (Gastropoda: Phyllidiidae) from the tropical south-west Pacific Ocean, in Bouchet P. & Marshall B.A.(Eds), Tropical Deep-Sea Benthos 22. Mémoires du Muséum national d'Histoire naturelle 185:331-368, ISBN:2-85653-527-5
Résumé [+]
[-]
Material collected by deep-sea expeditions in the south-west Pacific Ocean reveals a previously unrecognized radiation of the family Phyllidiidae into deeper waters, with a couple of species having a bathymetric range confined below 500 m. Whereas the shallow-water « 100 m) radiation consists mainly of species of Phyllidia, species of Phyllidiopsis make over 70% of the fauna in the 100-500 m interval, and the only two taxa recorded in the 500-750 m interval are species of Phyllidiopsis. A parallel pattern is observed in the Atlantic. There are no consistent anatomical differences between congeneric shallow and deep-water species, but taxa from deeper water are paler and have a simpler dorsal morphology. Twelve new species are described: Phyllidia orstomi sp. novo (Norfolk Ridge, 270-300 m), Phyllidiopsis brunckhorsti sp. novo (New Caledonia, 290350 m), P. anomalasp. Novo (Norfolk and Loyalty Ridges, 240-310 m), P. holothuriana sp. novo (Norfolk Ridge and Vanuatu, 110-240 m), P. macrotuberculata sp. novo (Norfolk Ridge, 270-300 m), P. futunai sp. novo (off Futuna 1., NE of Fiji, 165 245 m),P. crucifera sp. novo (off Futuna 1.,105-160 m), P. lozoueti sp. Novo (Norfolk Ridge, 235 m), P. richeri sp. novo (Norfolk Ridge, 510-750 m), P. circularis sp. novo (Norfolk Ridge, 510-530 m), P. vanuatuensis sp. novo (off Tanna 1., Vanuatu, 410 m), and P. neocaledonica sp. novo (New Caledonia, 315 m). Phyllidia varicosa var.quadrilineata Bergh, 1905, unrecorded since its description from the Flores Sea, Indonesia, is recognized as a valid species of Phyllidiopsis and recorded from Vanuatu in 160 -180 m.
Campagnes accessibles citées (11) [+]
[-]
BATHUS 1,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 2,
HALIPRO 1,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
SMIB 8
Codes des collections associés:
IM (Mollusques)
-
Valdés Á. 2002. Phylogenetic systematics of " Bathydoris " s.l. Bergh, 1884 (Mollusca, Nudibranchia), with the description of a new species from New Caledonian deep waters. Canadian Journal of Zoology 80(6): 1084-1099. DOI:10.1139/z02-085
Résumé [+]
[-]
There are six valid species in the traditional genus Bathydoris, all of them found in polar or deep waters: Bathydoris abyssorum Bergh, 1884 (from the deep equatorial Pacific Ocean), Bathydoris ingolfiana Bergh, 1899 (from Greenland), Bathydoris hodgsoni Eliot, 1907 (from Antarctic and subantarctic waters), Bathydoris clavigera Thiele, 1912 (from the Argentinean deep-sea basin and Antarctica), Bathydoris aioca Ev. Marcus and Er. Marcus, 1962 (from deep waters off California), and a new species, Bathydoris spiralis (from deep waters off New Caledonia). Bathydoris patagonica Kaiser, 1980 and Bathydoris violacea Baranets, 1993 are regarded as synonyms of B. hodgsoni and B. clavigera, respectively. Bathydoris spiralis is clearly distinguishable from other members of the genus mainly in having a triaulic reproductive system and a very elongated, spirally coiled deferent duct. Examination of the holotype of B. violacea revealed that it is a synonym of B. clavigera. Bathydoris vitjazi Minichev, 1969 is most likely a synonym of B. hodgsoni, but is provisionally regarded as nomen dubium until more material becomes available. The phylogenetic hypothesis supports the monophyly of the Anthobranchia but shows that the genus Bathydoris is paraphyletic. Species of Bathydoris are divided into two clades, one of them also containing the phanerobranch and cryptobranch dorids. Bathydoris type species B. abyssorum retains its name and diagnosis, but B. clavigera and B. spiralis are excluded from this genus. They are, however, provisionally maintained in "Bathydoris" s.l., a likely paraphyletic group. This result shows some incongruities between the traditional nomenclatural system and phylogenetic systematics.
Campagnes accessibles citées (5) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Valdés Á. 2008. Deep-sea “cephalaspidean” heterobranchs (Gastropoda) from the tropical southwest Pacific, in Héros V., Cowie R.H. & Bouchet P.(Eds), Tropical Deep Sea Benthos 25. Mémoires du Muséum national d'Histoire naturelle 196:587-792, ISBN:978-2-85653-614-8
Résumé [+]
[-]
One hundred and twenty-one species of deep sea “cephalaspidean” heterobranchs belonging to the genera Acteon, Crenilabium, Obrussena, Rictaxis, Japonacteon, Maxacteon, Bullina, Diaphana, Toledonia, Cylichna, Scaphander, Sabatia, Roxania, Cylichnium, Acteocina, Truncacteocina, Philine, Retusa, Pyrunculus, Volvulella, Relichna, Micratys, Gastropteron, Aglaja and Philinopsis are reported from the tropical southwest Pacifi c. Thirty-nine of these species are new: Acteon ionfasciatus, Acteon chrystomatus, Rictaxis sanguinea, Japonacteon longissimus, “Acteon” editus, “Acteon” buccinus, “Acteon” ringiculoides, “Acteon” boteroi, “Acteon” loyautensis, “Acteon” rhektos, “Acteon” profundus, “Acteon” osexiguus, “Acteon” aphyodes, “Acteon” herosae, “Acteon” comptus, “Acteon” chauliodous, “Acteon” cohibilis, Bullina rubropunctata, Toledonia neocaledonica, Toledonia epongensis, Cylichna tanyumphalos, Cylichna grovesi, Sabatia pyriformis, Roxania smithae, Cylichnium mucronatum, Cylichnium nanum, Acteocina lata, Philine habei, Philine babai, Philine abyssicola, Retusa diaphana, Retusa insolita, Retusa lenis, Retusa abyssicola, Retusa trunca, Volvulella onoae, Volvulella multistriata, Relichna hadra and Micratys wareni. A previously described species, Acteon aequatorialis, is included in the new genus Bathyacteon. Three species are assigned provisionally to already described species until more material becomes available: Acteon cf. nakayamai, Maxacteon cf. kawamurai, “Acteon” laetus. Thirty-eight species remain unnamed because of the absence of adequate information, but the shells are illustrated. Most species are described based on conchological data. Fourteen species of Acteonidae and two of Retusidae are provisionally assigned to the artifi cial taxa “Acteon” and “Retusidae” until anatomical data become available. The present collecting effort in the southwest Pacifi c has produced large numbers of previously undocumented species. The largest number of species was found in the area comprising the Coral Sea, New Caledonia, Vanuatu, Fiji, Tonga and Wallis and Futuna, which is probably a consequence of a greater collecting effort. The list of species refl ects a high degree of endemism in the deep sea fauna from the southwest Pacifi c. Only a few widespread Indo-Pacific species have been found in the deep sea. It also appears that there is some sort of isolation between the Coral Sea, New Caledonia, Vanuatu, Fiji, Tonga and Wallis and Futuna region and the Philippines and Indonesia region, which is refl ected in the small number of species shared between these two areas. Most species of “cephalaspidean” heterobranchs studied here have broad bathymetric ranges compared to other groups of opisthobranchs, which may be a result of a higher ecological adaptability of this group, or may be an artifact caused by transport of empty shells. When only specimens collected alive are considered, the bathymetric ranges of most species are considerably narrower. Most species studied are exclusively found in the deep sea, but a small number of shallow water species have been recorded here for the fi rst time in deep waters. When the ranges of empty shells are examined there appears to be a turnover of “cephalaspidean” heterobranch species at about 1000-1200 m depth and a blurry transition between shallow waters and the deep sea. When only specimens collected alive are considered, there is a sharp boundary at about 200 m that clearly separates the shallow water and the deep sea faunas. “Cephalaspidean” heterobranch species are more common relative to other groups of opisthobranchs in deep waters than in shallow waters, but this result may be an artefact caused by the collecting techniques.
Campagnes accessibles citées (35) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
Restreint,
CORINDON 2,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
LITHIST,
MUSORSTOM 10,
MUSORSTOM 2,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
PALEO-SURPRISE,
SMIB 2,
SMIB 3,
SMIB 5,
SMIB 8,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Vermeij G.J. & Bouchet P. 1998. New Pisaniinae (Mollusca, Gastropoda, Buccinidae) from New Caledonia, with remarks on Cantharus and related genera. Zoosystema 20(3): 471-485
Résumé [+]
[-]
The genera Cantharus Röding, 1798, Pollia Gray in Sowerby, 1834, and Cancellopollia n.g. (type species : C. gracilis n. sp.) are pisaniine buccinids having a small tooth (labral spine) at the edge of the crenulated outer lip. As defined and restricted here, these genera have a mainly Indo-West Pacific distribution. Cantharus septemcostatus n. sp. , Pollia pellita n. sp., Cancellopollia gracilis n. sp. , and C. ustulata n. sp., are reported from deep water in the New Caledonia region, and Cantharus leucotaeniatus Kosuge, 1985 and Pollia vicdani (Kosuge, 1984) n. comb. are from the Vanuatu. Despite a narrow bathymetric (4154-560 m) and horizontal (northernmost Norfolk Ridge) distribution, Cancellopollia gracilis exhibits remarkable variation, with highly localised morphs.
Campagnes accessibles citées (16) [+]
[-]
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
CHALCAL 2,
LAGON,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
SMIB 1,
SMIB 2,
SMIB 3,
SMIB 6,
SMIB 8,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Vidal J. & Kirkendale L. 2007. Ten new species of Cardiidae (Mollusca, Bivalvia) from New Caledonia and the tropical western Pacific. Zoosystema 29(1): 83-107
Résumé [+]
[-]
The fauna of the tropical Indo-west Pacific is exceptionally diverse but poorly known with even relatively well-studied faunal components yielding new species after careful study, novel approaches (e.g., delineation of cryptic species via molecular analyses) and/or rigorous collection efforts. In an attempt to quantify the biodiversity of the western Pacific molluscan fauna, comprehensive, systematic collecting expeditions have been made since 1978, with a focus on New Caledonia. Building on earlier studies of cardiids from the western Pacific, we report one new genus of cardiid (Pseudofulvia n. gen.) and 10 new cardiid taxa from the area: Acrosterigma capricorne n. sp., Fulvia (Fulvia) colorata n. sp., F. (F.) vepris n. sp., F. (Laevifulvia) subquadrata n. sp., F. (L.) imperfecta n. sp., Pseudofulvia caledonica n. gen., n. sp., P. arago n. gen., n. sp., Ctenocardia gustavi n. sp., C. fi jianum n. sp., C. (Microfragum) subfestivum n. sp. The new species are easily differentiated from conspecifics in details of hinge, dentition, lunular shape and area, rib number and/or rib ornamentation, but often diff er in gross morphological features, such as coloration, shape and size as well. Ctenocardia gustavi n. sp., C. (Microfragum) subfestivum n. sp. and Pseudofulvia caledonica n. gen., n. sp. are relatively large-bodied, with a wide distribution throughout the western Pacifi c. In contrast, Acrosterigma capricorne n. sp. and Pseudofulvia arago n. gen., n. sp. are known only from the Austral Islands and considering the intensive collecting efforts in the region, they appear restricted in their distributions.
Campagnes accessibles citées (26) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CORAIL 2,
LAGON,
LIFOU 2000,
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
PANGLAO 2004,
SALOMON 1,
SMIB 2,
Restreint,
VAUBAN 1978-1979
Codes des collections associés:
IM (Mollusques)
-
Vilvens C. & Maestrati P. 2006. New records and three new species of Thysanodonta (Gastropoda: Calliostomatidae: Thysanodontinae) from New Caledonia. Novapex 7(1): 1-11
Résumé [+]
[-]
New records of Thysanodonta from New Caledonia area are listed. Thysanodonta diadema n. sp., T. pileum n. sp. and T. cassis n. sp. are described and compared with similar Thysanodonta species from New Caledonia that are also illustrated. Seven Thysanodonta species are recognised by now in New Caledonia, a eighth species occuring in the neighbouring Chesterfield Islands.
Campagnes accessibles citées (10) [+]
[-]
Codes des collections associés:
IM (Mollusques)
-
Vilvens C. 2007. New species and new records of Calliotropis (Gastropoda: Chilodontidae: Calliotropinae) from Indo-Pacific. Novapex 8(H.S. 5): 1-72
Résumé [+]
[-]
New records of 25 Calliotropis species from the Indo-Pacific area are listed, extending the distribution area of some of them. 30 new species and 1 new subspecies are described and compared with similar Calliotropis species : C. conoeides n. sp.; C. helix n. sp.; C. cynee n. sp.; C. chalkeie n. sp.; C. ptykte n. sp.; C. solomonensis n. sp.; C. pistis n. sp.; C. echidnoides n. sp.; C. cycloeides n. sp.; C. pyramoeides n. sp.; C. coopertorium n. sp.; C. asphales n. sp.; C. nux n. sp.; C. oros n. sp.; C. oros marquisensis n. ssp.; C. zone n. sp.; C. hysterea n. sp.; C. stegos n. sp.; C. oregmene n. sp.; C. cooperculum n. sp.; C. keras n. sp.; C. denticulus n. sp.; C. dicrous n. sp.; C. rostrum n. sp.; C. pheidole n. sp.; C. siphaios n. sp.; C. nomisma n. sp.; C. nomismasimilis n. sp.; C. elephas n. sp.; C. ostrideslithos n. sp.; C. trieres n. sp.
Campagnes accessibles citées (39) [+]
[-]
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BORDAU 1,
BORDAU 2,
CALSUB,
CHALCAL 1,
CHALCAL 2,
CORAIL 2,
HALICAL 1,
HALIPRO 1,
HALIPRO 2,
KARUBAR,
LAGON,
MUSORSTOM 10,
MUSORSTOM 4,
MUSORSTOM 5,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
PALEO-SURPRISE,
SALOMON 1,
SMIB 1,
SMIB 10,
SMIB 2,
SMIB 3,
SMIB 4,
SMIB 5,
SMIB 6,
SMIB 8,
TAIWAN 2000,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Vilvens C. 2017. New species and new records of Chilodontidae (Gastropoda: Vetigastropoda: Seguenzioidea) from the Pacific Ocean. Novapex 18(HS 11): 1-67
Résumé [+]
[-]
New records of Chilodontidae species described from various Pacific localities are listed, extending their distribution.
15 new species are described from New Caledonia, Fiji, French Polynesia, Solomon Islands and Taiwan, and compared with similar species: Vaceuchelus cavernoides n. sp., V. phaios n. sp., V. rapaensis n. sp., Herpetopoma pantantoi n. sp., H. vitilevuense n. sp., H. hivaoaense n. sp., Euchelus polysarkon n. sp., Ascetostoma pteroton n. sp., Clypeostoma chranos n. sp., C. adelon n. sp., Pholidotrope asteroeides n. sp., P. choiseulensis n. sp., Danilia stroggylon n. sp., Perrinia cantharidoides n. sp. and P. guadalcanalensis n. sp.
Two new synonymies are established: Vaceuchelus saguili Poppe, Tagaro & Dekker, 2006 from the Philippines is synonymized with V. favosus (Melvill & Standen, 1896), and V. vangoethemi Poppe, Tagaro & Dekker, 2006 from the Philippines is synonymized with V. clathratus (A.Adams, 1853)
Campagnes accessibles citées (49) [+]
[-]
AURORA 2007,
BATHUS 1,
BATHUS 2,
BATHUS 3,
BATHUS 4,
BENTHAUS,
BERYX 11,
BIOCAL,
BIOGEOCAL,
BOA0,
BOA1,
BORDAU 1,
BORDAU 2,
CHALCAL 1,
CHALCAL 2,
CONCALIS,
CORAIL 2,
EBISCO,
KARUBAR,
LAGON,
LIFOU 2000,
Restreint,
MONTROUZIER,
MUSORSTOM 10,
MUSORSTOM 3,
MUSORSTOM 4,
MUSORSTOM 6,
MUSORSTOM 7,
MUSORSTOM 8,
MUSORSTOM 9,
NORFOLK 1,
NORFOLK 2,
PALEO-SURPRISE,
PANGLAO 2004,
PANGLAO 2005,
RAPA 2002,
SALOMON 1,
SALOMON 2,
SALOMONBOA 3,
SANTO 2006,
SMIB 3,
SMIB 8,
Restreint,
Restreint,
TAIWAN 2000,
TAIWAN 2001,
TAIWAN 2002,
VAUBAN 1978-1979,
VOLSMAR
Codes des collections associés:
IM (Mollusques)
-
Williams S.T., Smith L., Herbert D.G., Marshall B.A., Warén A., Kiel S., Dyal P., Linse K., Vilvens C. & Kano Y. 2013. Cenozoic climate change and diversification on the continental shelf and slope: evolution of gastropod diversity in the family Solariellidae (Trochoidea). Ecology and Evolution 3(4): 887-917. DOI:10.1002/ece3.513
Résumé [+]
[-]
Recent expeditions have revealed high levels of biodiversity in the tropical deep-sea, yet little is known about the age or origin of this biodiversity, and large-scale molecular studies are still few in number. In this study, we had access to the largest number of solariellid gastropods ever collected for molecular studies, including many rare and unusual taxa. We used a Bayesian chronogram of these deep-sea gastropods (1) to test the hypothesis that deep-water communities arose onshore, (2) to determine whether Antarctica acted as a source of diversity for deep-water communities elsewhere and (3) to determine how factors like global climate change have affected evolution on the continental slope. We show that although fossil data suggest that solariellid gastropods likely arose in a shallow, tropical environment, interpretation of the molecular data is equivocal with respect to the origin of the group. On the other hand, the molecular data clearly show that Antarctic species sampled represent a recent invasion, rather than a relictual ancestral lineage. We also show that an abrupt period of global warming during the Palaeocene Eocene Thermal Maximum (PETM) leaves no molecular record of change in diversification rate in solariellids and that the group radiated before the PETM. Conversely, there is a substantial, although not significant increase in the rate of diversification of a major clade approximately 33.7Mya, coinciding with a period of global cooling at the EoceneOligocene transition. Increased nutrients made available by contemporaneous changes to erosion, ocean circulation, tectonic events and upwelling may explain increased diversification, suggesting that food availability may have been a factor limiting exploitation of deep-sea habitats. Tectonic events that shaped diversification in reef-associated taxa and deep-water squat lobsters in central Indo-West Pacific were also probably important in the evolution of solariellids during the Oligo-Miocene.
Campagnes accessibles citées (19) [+]
[-]
AURORA 2007,
BENTHAUS,
BERYX 11,
BIOPAPUA,
BOA1,
BORDAU 1,
CONCALIS,
EBISCO,
MAINBAZA,
MIRIKY,
NORFOLK 1,
NORFOLK 2,
PANGLAO 2004,
PANGLAO 2005,
SALOMON 1,
SALOMON 2,
TAIWAN 2001,
TARASOC,
TERRASSES
Codes des collections associés:
IM (Mollusques)
-
Yang C.H., Chen I.S. & Chan T. 2011. A new slipper lobster of the genus Galearctus Holthuis, 2002 (Crustacea, Decapoda, Scyllaridae) from New Caledonia. Zoosystema 33(2): 207-217. DOI:10.5252/z2011n2a4
Résumé [+]
[-]
Material previously identified as Galearctus kitanoviriosus (Harada, 1962) from New Caledonia has been found to consist of two distinct species. These species differ in the shape of the gastric tooth, third pereiopod propodus, antennal segment IV and thoracic sternum. The shallow water form is the true G. kitanoviriosus, while the deep-water form is new to science. Genetic comparison of the sequence of the barcoding gene, mitochondrial cytochrome c oxidase subunit (COI), also supports the separation.
Campagnes accessibles citées (7) [+]
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Codes des collections associés:
IU (Crustacés)
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Yang C.H., Bracken-grissom H., Kim D., Crandall K.A. & Chan T.Y. 2012. Phylogenetic relationships, character evolution, and taxonomic implications within the slipper lobsters (Crustacea: Decapoda: Scyllaridae). Molecular Phylogenetics and Evolution 62(1): 237-250. DOI:10.1016/j.ympev.2011.09.019
Résumé [+]
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The slipper lobsters belong to the family Scyllaridae which contains a total of 20 genera and 89 species distributed across four subfamilies (Arctidinae, Ibacinae, Scyllarinae, and Theninae). We have collected nucleotide sequence data from regions of five different genes (16S, 18S, COI, 28S, H3) to estimate phylogenetic relationships among 54 species from the Scyllaridae with a focus on the species rich subfamily Scyllarinae. We have included in our analyses at least one representative from all 20 genera in the Scyllaridae and 35 of the 52 species within the Scyllarinae. Our resulting phylogenetic estimate shows the subfamilies are monophyletic, except for Ibacinae, which has paraphyletic relationships among genera. Many of the genera within the Scyllarinae form non-monophyletic groups, while the genera from all other subfamilies form well supported clades. We discuss the implications of this history on the evolution of morphological characters and ecological transitions (nearshore vs. offshore) within the slipper lobsters. Finally, we identify, through ancestral state character reconstructions, key morphological features diagnostic of the major clades of diversity within the Scyllaridae and relate this character evolution to current taxonomy and classification. (C) 2011 Elsevier Inc. All rights reserved.
Campagnes accessibles citées (2) [+]
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Codes des collections associés:
IU (Crustacés)