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.

???msg.security.private???, ATIMO VATAE, ???msg.security.private???, ???msg.security.private???, BATHUS 1, BATHUS 3, BATHUS 4, BENTHAUS, BERYX 11, BERYX 2, BIOCAL, ???msg.security.private???, BIOPAPUA, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, ???msg.security.private???, HALIPRO 1, HALIPRO 2, ???msg.security.private???, KARUBAR, ???msg.security.private???, 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

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

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.

???msg.security.private???, BERYX 11, BERYX 2, HALICAL 1, HALIPRO 1, HALIPRO 2

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.

AZTEQUE, BATHUS 1, BERYX 11, BERYX 2, BIOCAL, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 7, SMIB 3

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.

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

The description and comparative characteristic of three vicariated Indo-West Pacific species from the genus Nematocarcinus (N. tenuirostris Bate 1888 and N. pseudocersor Burukovsky, 1990 are previously known; N. alisae Burukovsky s. n. is new) are given. They are distinguished from other known species of the genus by similarity in structure of the distro-ventral organ of the 6th abdominal segment. In these species, spots of the distro-ventral organ are located on an original protuberance forming in the distal quarter of ventral segment surface - blister. The spots are always located in close proximity to each other. These species are primarily distinguished by their rostrum structure.

BATHUS 1, BATHUS 3, BERYX 2, BIOCAL, HALIPRO 1, HALIPRO 2, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 5, MUSORSTOM 7, MUSORSTOM 8

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.

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

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.

AURORA 2007, AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHEDI, BERYX 11, BERYX 2, BIOCAL, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, CHALCAL 1, CHALCAL 2, ???msg.security.private???, EBISCO, EXBODI, HALIPRO 1, KARUBAR, LITHIST, MAINBAZA, ???msg.security.private???, MIRIKY, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PALEO-SURPRISE, PANGLAO 2005, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006, SMCB, SMIB 1, SMIB 2, SMIB 4, SMIB 8, TAIWAN 2001, TARASOC, TERRASSES, VAUBAN 1978-1979, VOLSMAR

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

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.

???msg.security.private???, 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, ???msg.security.private???, ???msg.security.private???, SMIB 1, SMIB 10, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, SMIB 9, ???msg.security.private???, TAIWAN 2000, VAUBAN 1978-1979, VOLSMAR

AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BERYX 2, BIOCAL, CHALCAL 1, CHALCAL 2, GEMINI, HALIPRO 1, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, SMCB, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, VOLSMAR

BERYX 11, BERYX 2, BIOCAL, CHALCAL 1, CHALCAL 2, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6

AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 11, BERYX 2, BIOCAL, BIOGEOCAL, CHALCAL 1, CHALCAL 2, CONCALIS, CORAIL 2, EBISCO, HALICAL 1, HALIPRO 2, LAGON, LIFOU 2000, LITHIST, MONTROUZIER, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, SMIB 8

BERYX 2

BERYX 11, BERYX 2, CHALCAL 1, HALIPRO 1, LAGON

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.

???msg.security.private???, 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

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.

AZTEQUE, ???msg.security.private???, BATHUS 1, BATHUS 2, BATHUS 3, BENTHEDI, BERYX 11, BERYX 2, BIOCAL, BIOGEOCAL, CHALCAL 1, CHALCAL 2, CORAIL 2, CORINDON 2, ???msg.security.private???, 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

BERYX 11, BERYX 2, BIOCAL, CHALCAL 2, LITHIST, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 2, SALOMON 2

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.

BERYX 11, BERYX 2, CHALCAL 2, LITHIST

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.

BERYX 11, BERYX 2

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.

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

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.

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

BATHUS 2, BATHUS 3, BATHUS 4, BERYX 2, BIOCAL, CHALCAL 2, CORAIL 2, HALIPRO 2, LAGON, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, ???msg.security.private???, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, VAUBAN 1978-1979, VOLSMAR

Members of the benthopelagic fish family Euclichthyidae, also known as the Eucla cods, occur on the upper continental slopes off Australasia at 220–1040 m depths. Euclichthyids essentially differ from other gadiform fishes in a combination of two almost contiguous dorsal fins with the second much longer based, a deeply notched anal fin with its anterior portion greatly elevated, jugular pelvic fins consisting of 3 partly united filiform upper rays and 3 free filamentous lower rays, an asymmetrical caudal fin with 5 hypurals fused into two plates, and no chin barbel, or vomerine and palatine tooth patches. Additional characters attributed to the group by other published studies include: no horizontal diaphragm within the posterior chamber of the swim bladder, no swim bladder-auditory capsule connection, presence of a luminous organ, and cranial muscle adductor arcus palatini divided by a strong ligament running from the lateral ethmoid and palatine to the medial face of the hyomandibular. Widely considered to be monotypic since its erection in 1984, the group consists of a single genus and three allopatric species, Euclichthys polynemus McCulloch, 1926 (Western and southern Australia, New Zealand), and two new taxa, E. microdorsalis sp. nov. (northeastern Australia) and E. robertsi sp. nov. (eastern Australia and New Caledonia). Eucla cods are morphologically conservative with both new species superficially resembling the type species, E. polynemus. Euclichthys microdorsalis sp. nov. is the most anatomically and morphologically divergent member of the group in having a shorter first dorsal fin, longer snout, relatively small eye compared to its interorbital width, and fewer caudal-fin rays and primary rakers on the outer gill arch than its congeners. Euclichthys robersti sp. nov. differs from E. polynemus in being smaller with a more slender head, and having a smaller eye, longer anal-fin base and tail, smaller scales, fewer primary rakers on the outer gill arch, more elongate oval otoliths, and usually having a X and/or Y bone in the caudal skeleton (both absent in other Euclichthys). Little is known of their biology but available material suggest that early juveniles remain pelagic in the open ocean with adults benthopelagic near the sea floor. Diagnoses and a key are provided for the three species.

BERYX 2, CHALCAL 2

BERYX 11, BERYX 2

BERYX 11, BERYX 2

AZTEQUE, BERYX 11, BERYX 2

BERYX 11, BERYX 2

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.

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

A molecular phylogenetic analysis of the genus Hippasteria, rooted against Evoplosoma, has provided the basis for taxonomic revisions and provided insight into the biogeography of a widely occurring, cold-water group of corallivorous asteroids. Herein, we describe three new species, Hippasteria mcknighti sp. nov., Hippasteria muscipula sp. nov., and Hippasteria tiburoni sp. nov., from deep-water settings. Additionally, in light of taxonomic changes, we further elaborate on distribution data for multiple species. Range extensions for Hippasteria phrygiana and Hippasteria californica are included. Discussions about biogeography, cladogenic events, and morphology are also presented.(c) 2014 The Linnean Society of London

BERYX 2, MD08 (BENTHOS), MD24 (BIOMASS), MD30 (BIOMASS CROZET), MD42 (SIBEX), SALOMONBOA 3

BERYX 11, BERYX 2, BIOCAL, CHALCAL 1, CHALCAL 2, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6

The larvae of two species of the pylochelid genus Trizocheles are described from prematurely hatched specimens and compared with earlier described larvae of Pylocheles (Pylocheles) and Pomatocheles. Although all are lecithotrophic and exhibit marked advanced development, differences in the larval morphology among the three genera are profound. Consideration is given to these differences as they relate to development in the entire Paguroidea, and the possible impact they may have on pylochelid phylogeny. As one of the Trizocheles species is undescribed, adults as well as larvae are described and illustrated.

BERYX 2, BIOCAL, CHALCAL 2, EBISCO, NORFOLK 2, SALOMON 2, SMIB 3, SMIB 4

A new classification is presented based on the results of the recently completed cladistic analysis of the Pylochelidae. The subfamilies Pylochelinae and Pomatochelinae are retained, the latter with the genera Pylocheles and Cheiroplatea; however, the subgenera Xylocheles and Bathycheles are elevated to generic rank together with the nominal subgenus Pylocheles. In addition, one new species, B. phenax, is described in Bathycheles and B. profundus is shown to be conspecific with B. integer. The subfamilies Parapylochelinae, Cancellochelinae, Trizochelinae, and Mixtopagurinae are reduced to ranks of tribes and included in the subfamily Trizochelinae. A new genus Forestocheles is proposed in the tribe Trizochelini. Within the genus Trizocheles, subspecific rank for T. spinosus bathamae is deemed unjustified and this taxon is placed in synonymy with the nominal subspecies T spinosus spinosus. The correct identity of Trizocheles balssi is established and the species mistakenly thought to represent that taxon is described as T. hoensonae, new species. Trizocheles gracilis is found to be conspecific with T. boasi and an additional new species, T. mendanai, is added to the genus. The superfamilial ranks of Cheiroplateoidea, Pomatocheloidea, Pylocheloidea, and Cancellocheloidea proposed by Watabe (2007) are rejected, as is Birgusoidea.

AURORA 2007, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHEDI, BERYX 2, BIOCAL, BIOGEOCAL, BORDAU 1, BORDAU 2, CHALCAL 2, CORINDON 2, EBISCO, HALIPRO 1, LAGON, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, NORFOLK 2, PANGLAO 2004, PANGLAO 2005, SALOMON 1, SALOMON 2, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 8, TAIWAN 2000, TAIWAN 2002, TAIWAN 2003, TAIWAN 2004, VAUBAN 1978-1979

Although this paper concerns a large collection of dromiid crabs from the Philippine Islands and New Caledonia, with a few specimens from Indonesia and Hawaii, the opportunity is taken to review and revise most of the genera of the Dromiidae. The basis of the revision involves a much wider range of characters than have been used before. Excessive emphasis on the nature of the female sternal grooves is abandoned, and more attention is paid to relative dimensions and ornamentation of the carapace, arrangement of spines on and around the dactyli of all the legs, fusion of the last two segments of the abdomen, and size of the uropod plates. A new set of characters describing the second antenna and the male abdominal locking mechanism are also used. The impxDrtance of the cheliped epipod character is discussed and is shown to be variable in some genera. A total of 28 genera are defined or redefined and a key to their identification is provided, along with keys to the identification of 99 species in these genera. The following genera are restricted and/or redefined : Cryptodromia Stimpson, 1858, Cryptodromiopsis Borradaile, 1903, Dromia Weber, 1795, Dromidia Stimpson, 1858, Dromidiopsis Borradaile, 1900, Epigodromia (a replacement name for Epidromia Kossmann, 1818, which is preoccupied), Homalodromia Miers, 1884, Paradromia Balss, 1921, Petalomera Stimpson, 1858, and Pseudodromia Stimpson, 1858, resulting in the creation of 10 new genera. Ascidiophilus Richters, 1880, Conchoecetes Stimpson, 1858, Epipedodromia Andre, 1932, Eudromidia Barnard, 1947, Exodromidia Stebbing, 1905, Hemisphaerodromia Barnard, 1954, Hypoconcha Guerin-M6neville, 1854, Speodromia Barnard, 1947, and Sphaerodromia Alcock, 1899, remain unmodified. After the elimination of many synonyms and together with the new material described herein, the Dromiidae now includes 29 genera and 109 species. The generic revision has major implications for the dromiid crabs of, not only the Philippines and New Caledonia but also, the rest of the Indo-Pacific region, Australia, South Africa, and the Atlantic. Until now only six species of dromiid crabs were known from New Caledonia and the Philippine Islands. This number is increased to 29 species belonging to 13 genera. The most common species are Lauridromia intermedia (Laurie, 1906) nov. comb., Petalomera pulchra Miers, 1884, Cryptodromia coronata Stimpson, 1858, Dromidiopsis dubia Lewinsohn, 1984, and Epigodromia areolata (Ihle, 1913) nov. comb. Most of these dromiids come from shallow water, less than 100 m, and the maximum number of sp)ecies occurs in the depth interval of 30-60 m. The greatest depth of 437 m is shown by Frodromia atypica (Sakai, 1936) nov. comb. There is a large range of body size from a few millimetres, for Homalodromia coppingeri, to around 200 mm CW, for Dromia dormia. Egg size ranges from 0.4 mm to 1.1 mm diameter but there is no evidence of direct development amongst these dromiids. The apparent biogeographic affinities of the dromiids from New Caledonia and the Philippines are, in decreasing order, with Japan, Indian Ocean, Indonesia, and Australia. The apparent affinity with Japan may well be an artifact of more intensive collecting. The most wide ranging species are Lauridromia intermedia (Laurie, 1906), Dromia dormia (Linnaeus, 1763), D. wilsoni (Fulton & Grant, 1902) nov. comb., Cryptodromiopsis unidentata (Riippell, 1830) nov. comb., Cryptodromia hilgendorfi De Man, 1888, and C. fallax (Lamarck, 1818) nov. comb. These species also represent the most wide ranging genera. The collection of species largely consists of widely distributed species typical of an island fauna.

BERYX 2, CHALCAL 1, CORAIL 2, KARUBAR, LAGON, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, SMIB 5, SMIB 6, VOLSMAR

Two new deep water Coelorinchus species were captured during a joint Australia/New Zealand marine fauna survey of the West Norfolk and South Norfolk Ridges and south Lord Howe Rise in May-June 2003. Coelorinchus Osipullus sp. Nov. Is similar to the Australasian C. celaenostomus McMillan and Paulin and had been mistakenly identified as such in French collection surveyx off New Caledonia and the Loyalty Islands, but the new species has pale to dusky lips and mouth compared to the intense black markings of C. celaenostomus. It is also very similar to C. sheni Chiou, Shao, and Iwamoto from Taiwan, but has shorter and narrower snout and blackish gums compared to the pale gums of C. sheni. Coelorinchus obscuratus sp. Nov. Is most similar to C. occa (Goode and Bean) from the western North Atlantic, but the latter has a larger orbit, lacks a blackish orbital rim, and has much more coasely spinnulated scales.

BERYX 2, HALIPRO 2

Deep-water trawl surveys on seamounts around New Caledonia yielded 62 specimens of the little-known genus, Scaeurgus. Members of this genus of octopuses typically occur at depths of 200-500 m in temperate and tropical latitudes worldwide. Prior to this study, Scaeurgus was considered to contain one to two species. The new material from New Caledonia contained a surprising diversity of Scaeurgus species from a small area: three distinct new species are described and limited material of a further two taxa is reported. A pygmy member of this genus is reported for the first time. Distributions of these new taxa are consistent with reports of high endemism on the seamount systems in this region. Fifty-eight of the 62 specimens were collected from seamounts, with four of the five taxa unique to a single seamount.

BATHUS 3, BERYX 2, CHALCAL 1, LITHIST, MUSORSTOM 5, NORFOLK 1, SMIB 8

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.

AZTEQUE, BATHUS 1, BERYX 11, BERYX 2, CHALCAL 2, MUSORSTOM 4, MUSORSTOM 5, SMIB 3, SMIB 4

BERYX 2

AZTEQUE, BERYX 2, GEMINI, SMIB 5, SMIB 6, VOLSMAR

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

A rapid panorama of the deep sea fauna knowledge, deeper than 100 m, is shown, positioning the specific richness and sampling New Caledonia effort in the Indo-Pacific. A detailled presentation of the french exploration oceanographic cruises is done. Since 1984, no less than 1468 benthic samples in the New Caledonia EEZ have been done. All these data are now integrated in the "Océane" database at IRD Center in Noumea. This document give an inventory of 2515 deep sea species from New Caledonia, presented by zoological groups and families by alphabetic order. 1322 new species were described from New Caledonia (52.5%). ln annexe is given: a complete list of references corresponding to the description of this fauna and the list of taxonomists involved (155 scientists from 21 countries); the bathymetric maps of the main seamounts.

AZTEQUE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BERYX 2, BIOCAL, BIOGEOCAL, BORDAU 1, BORDAU 2, CHALCAL 1, CORAIL 2, CORINDON 2, ???msg.security.private???, GEMINI, HALIPRO 1, KARUBAR, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, VOLSMAR

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.

BERYX 11, BERYX 2, CHALCAL 2

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.

BERYX 11, BERYX 2, CHALCAL 2, MUSORSTOM 4, MUSORSTOM 5

The Australasian sandfish, Gonorynchus forsteri Ogilby, is recorded for lhe first time from the New Caledonian Exclusive Economic Zone (EEZ). The record is based on two adult specimens, one running ripe female and one spent or resting male, captured at 960-1233 m depth on the Loyalty Island Ridge and Lord Howe Rise. Their presence in bathyal depths over 700 nautical miles from the nearest known populations is discussed and compared with the occurrence of the species in New Zealand waters. It is hypothesized that adult sandfish migrate along oceanic ridges to spawn in southern New Caledonian waters.

BERYX 2, HALIPRO 2

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).

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, ???msg.security.private???, SMIB 8

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

Secondary metabolites often play an important role in the adaptation of organisms to their environment. However, little is known about the secondary metabolites of ancient organisms and their evolutionary history. Chemical analysis of exceptionally well-preserved colored fossil crinoids andmodern crinoids from the deep sea suggests that bioactive polycyclic quinones related to hypericin were, and still are, globally widespread in post-Paleozoic crinoids. The discovery of hypericinoid pigments both in fossil and in presentday representatives of the order Isocrinida indicates that the pigments remained almost unchanged since the Mesozoic, also suggesting that the original color of hypericinoid-containing ancient crinoids may have been analogous to that of their modern relatives. The persistent and widespread occurrence, spatially as well as taxonomically, of hypericinoid pigments in various orders during the adaptive radiation of post-Paleozoic crinoids suggests a general functional importance of the pigments, contributing to the evolutionary success of the Crinoidea.

BERYX 2, PANGLAO 2005, VAUBAN 1978-1979