Taxonomic and ecological interest in squat lobsters has grown considerably over the last two decades. A checklist of the 870 current valid species of squat lobsters of the world (families Chirostylidae, Galatheidae and Kiwaidae) is presented. The compilation includes the complete taxonomic synonymy and geographical distribution of each species plus type information (type locality, repository and registration number). The numbers of described species in the world's major ocean basins are summarised.

BENTHAUS, BIOCAL, Restricted, BORDAU 1, BORDAU 2, CHALCAL 2, CORAIL 2, Restricted, HALIPRO 2, Restricted, KARUBAR, MD32 (REUNION), 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, SMCB, SMIB 3, SMIB 4, SMIB 5, SMIB 8, VOLSMAR

In a previous phylogenetic analysis of numerous species of the genus Munida and related genera from the West Pacific based on molecular and morphological data, the monophyly of this group with the exception of M. callista was established. Morphologically, M. callista is closely related to M. brucei, M. javieri, M. hystrix and M. plexaura showing morphological differences in the shape of the rostrum, the supraocular spines, and the ridges on the epistome with respect to the genus Munida. Moreover, the analysis of the mitochondrial genes 16S rRNA and COI showed an independent and monophyletic lineage from the genus Munida. Therefore a new genus, Babamunida, is proposed to accommodate these five species, based on morphological characters and molecular data.

BENTHAUS, BIOCAL, KARUBAR, MUSORSTOM 9, NORFOLK 2, SALOMON 2

The family Galatheidae is among the most diverse families of anomuran decapod crustaceans, and the South-West Pacific is a biodiversity hot spot for these squat lobsters. Attempts to clarify the taxonomic and evolutionary relationships of the Galatheidae on the basis of morphological and molecular data have revealed the existence of several cryptic species, differentiated only by subtle morphological characters. Despite these efforts, however, relationships among genera are poorly understood, and the family is in need of a detailed systematic review. In this study, we assess material collected in different surveys conducted in the Solomon Islands, as well as comparative material from the Fiji Islands, by examining both the morphology of the specimens and two mitochondrial markers (cytochrome oxidase subunit 1, COI, and 16S rRNA). These two sources of data revealed the existence of eight new species of squat lobster, four of which were ascribed to the genus Munida, two to the genus Paramunida, one to the genus Plesionida, and the last species was ascribed to the genus Agononida. These eight species are described along with phylogenetic relationships at the genus level. Our findings support the taxonomic status of the new species, yet the phylogenetic relationships are not yet fully resolved. Further molecular analysis of a larger data set of species, and more conserved genes, will help clarify the systematics of this group. (C) 2009 The Linnean Society of London, Zoological Journal of the Linnean Society, 2009, 156, 465-493.

BATHUS 1, BORDAU 1, HALIPRO 1, HALIPRO 2, MUSORSTOM 10, SALOMON 1, SALOMON 2

The genus Paramunida belongs to the family Galatheidae, one of the most species rich families among anomuran decapod crustaceans. In spite of the genus has received substantial taxonomic attention, subtle morphological variations observed in numerous samples suggest the existence of undescribed species. The examination of many specimens collected during recent expeditions and morphological and molecular comparisons with previously described species have revelaled the existence of eleven new lineages. All of them are distinguished by subtle and constant morphological differences, which are in agreement with molecular divergences reported for the mitochondrial markers ND1 and 16S rRNA. Here, we describe and illustrate the new species, providing brief redescriptions for the previously known species, and a dichotomous identification key for all species in the genus.

BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BIOCAL, BOA0, BORDAU 1, BORDAU 2, CORINDON 2, EBISCO, HALIPRO 1, KARUBAR, LIFOU 2000, MAINBAZA, MD08 (BENTHOS), 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 2005, SALOMON 1, SALOMON 2, SANTO 2006, TAIWAN 2004

The genus Allogalathea was established by Baba in 1969 to include the well-known species Galathea elegans. This species is widely distributed across the Indo-West Pacific Ocean, and is characterized by living in close association with crinoids, and by its conspicuous coloration. Although the genus is considered monospecific, different colour patterns and discrete morphological variations mainly associated with the rostrum and chelipeds have been reported. These differences could point to cryptic species, thereby questioning Allogalathea as a monotypic taxon. To address this issue, we sequenced the mitochondrial cytochrome oxidase I (COI; 658 bp) and 16S rRNA (882 bp) genes and the nuclear gene phosphoenolpyruvate carboxykinase (PEPCK; 598 bp) in numerous specimens from eight different localities, and also examined their morphological characters. DNA sequences were analysed using maximum-parsimony, maximum-likelihood, and Bayesian approaches of phylogenetic inference. The resulting trees were combined with morphological evidence to test species boundaries. Our molecular data revealed four deeply divergent clades, which can be distinguished by subtle morphological differences in the spinulation and length: breadth ratio of the P1 carpus, spinulation of the walking legs, and shape of the rostrum. Our findings indicated that Allogalathea elegans is in fact a species complex comprising four different species, which, although genetically very distinct, are morphologically very similar. We provide morphological descriptions and a key to these four species of the genus.

CORAIL 2, LAGON, LIFOU 2000, MAINBAZA, MD32 (REUNION), MONTROUZIER, MUSORSTOM 3, SANTO 2006, SMIB 5, VAUBAN 1978-1979

The diversification of Indo-Pacific marine fauna has long captivated the attention of evolutionary biologists. Previous studies have mainly focused on coral reef or shallow water-associated taxa. Here, we present the first attempt to reconstruct the evolutionary historyphylogeny, diversification, and biogeographyof a deep-water lineage. We sequenced the molecular markers 16S, COI, ND1, 18S, and 28S for nearly 80% of the nominal species of the squat lobster genus Paramunida. Analyses of the molecular phylogeny revealed an accelerated diversification in the late OligoceneMiocene followed by a slowdown in the rate of lineage accumulation over time. A parametric biogeographical reconstruction showed the importance of the southwest Pacific area, specifically the island arc of Fiji, Tonga, Vanuatu, Wallis, and Futuna, for diversification of squat lobsters, probably associated with the global warming, high tectonic activity, and changes in oceanic currents that took place in this region during the OligoceneMiocene period. These results add strong evidence to the hypothesis that the Neogene was a period of major diversification for marine organisms in both shallow and deep waters.

BATHUS 2, BATHUS 4, BENTHAUS, BOA0, BORDAU 1, BORDAU 2, EBISCO, HALIPRO 1, KARUBAR, LIFOU 2000, MD08 (BENTHOS), MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, SALOMON 1, SALOMON 2, SANTO 2006

The genus Paramunida belongs to the most diverse family of galatheoids and it is commonly reported from the continental slope across the Indian and Pacific Oceans. Examination of material collected by the NOAA RV Townsend Cromwell Cruise near Christmas (Kiritimati) Island, Kiribati, revealed the existence of a new species of Paramunida (P. haigae), which represents the fourth record of the genus for the Central Pacific. Furthermore, recent efforts to unravel phylogenetic relationships and diversification patterns in Paramunida revealed P. granulata (Henderson, 1885) to be the most basally diverging taxon within the genus. This species is clearly distinguished from other species of Paramunida by the spinulation of the carapace and the length of the distomesial spine of the second antennal peduncle article, which in combination with a high level of genetic divergence suggest that this species represents a separate monotypic lineage. A new genus, Hendersonida gen. n., is proposed to accommodate this species based on morphological and molecular evidence. An updated dichotomous identification key for all species of Paramunida is presented.

BATHUS 2

The genus Eumunida, belonging to the family Chirostylidae, is represented in New Caledonia and Chesterfield Islands by seven species, ail of them new to Science : Eumunida keijii, E. sternomaculata, E. annulosa, E. capillata, E. parva, E. minor and E. marginata. Four species (E. sternomaculata, E. annulosa, E. capillata, and E. parva) are very common at depths between 400 and 600 meters, being currently caught at the same stations. The other species are scarce, and hâve been collected either at the same depths (E. keijii), or in shallower waters (E. minor and E. marginata). The high abundance of thèse species could be related to the présence on the bottom of hydrocorallians of the family Stylasteridae. Three species (E. keijii, E. annulosa and E. sternomaculata) belong to the group A after GORDON (1930), characterized by a spine on either side of the sternal segment bearing the chelipeds. The latter two of thèse species hâve a pad on the ventral surface of the palm. E. keijii is closely related to E. pacifica Gordon, 1930, from the south of Timor, but, among other différences, the two are readily distinguished by the size of the first hepatic spine, the médian sinus of the third thoracic sternite and the scales on the sternal segments. E. sternomaculata resembles E. sp., from southeast Australia (E. picta, GORDON, 1930, in part) ; both are nevertheless easily distinguished by the shape of the frontal part of the carapace, the direction of the supraorbital spines and the relative lengths of the anterolateral spines and antennal peduncles. E. annulosa is close to E. sternomaculata. Thèse two species are differentiated by the shape of the rostral spines, the ornamentation of the carapace, the length and shape of the chelipeds and the présence or absence of a disto-mesial spine on the carpus of the chelipeds. E. marginata, E. capillata, E. parva and E. minor belong to the group B, after GORDON, that has no spine on either side of the sternal segment bearing the chelipeds. With the exception of E. parva, ail the other species are provided with a pad on the ventral surface of the palm. E. parva is closely related to E. smithii Henderson, 1883, from the south of Timor, and to E. propior Baba, 1988, from the Philippines. A discussion about the identity of the material of E. smithii from différent expéditions and the relationships between the three species is provided. The maies of thèse three species are characterized by the présence of pleopods on the second to fifth abdominal segments. E. capillata is very close to E. parva, but can be easily distinguished from it by a number of characters. The main différence is the présence of a pad on the ventral surface of the cheliped palm in capillata, and its absence in parva. E. minor is the smallest représentative of the genus. The species is clearly distinguishable from ail the others of the group B by the présence of two prominent spines on the merus of the third maxillipeds, and of four longitudinal rows of spines on the merus of the cheliped. Its closest relative is E. balssi Gordon, 1930. E. marginata is related to E. gordonae Baba, 1973, from Japan. However, the length and the spinulation of the pereopods are very different.

BIOCAL, CHALCAL 2, LAGON, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, SMIB 1, SMIB 2, SMIB 3

The first zoeal stages of the galatheids Neonida grandis, Agononida squamosa and Munida javieri, and the chirostylids Eumunida annulosa and E. capillata are described and illustrated from laboratory-hatched material obtained from ovigerous females collected from south western Pacific. The morphologies of the first zoeae are compared with the same larval stage of other known anomuran species. The larval characters of Agononida squamosa and Neonida grandis are similar to those described for Agononida incerta. Munida javieri exhibits features not present in other described species of Munida such as the setation of the endopod of the maxillule and the antennal morphology. Eumunida annulosa and E. capillata do not show abbreviated development as in other described chirostylids such as Uroptychus and Gastroptychus, and its larval morphology is equivalent to the first stage of galatheid zoeae. However, many morphological characters of E umunida species are typically pagurid, such as the two terminal plumose setae of the antennal endopod, the three-segmented endopod of the maxillule, the posterior margin of the carapace without spines, and the scaphognathite with 5 plumose setae and without a posterior lobe.

BOA1, NORFOLK 2

BATHUS 2, BATHUS 3, BATHUS 4, BIOCAL, BORDAU 1, CHALCAL 2, HALICAL 1, HALIPRO 2, LAGON, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, SALOMON 1, SMIB 8

Unravelling the evolutionary history of taxa requires solid delimitation of the traits characterising these. This can be challenging especially in groups with a highly complex taxonomy. The squat lobster family Munididae contains more than 450 species distributed among 21 genera, Munida being the most speciose (~300 species). Previous phylogenetic studies, based on a small part of the diversity of the group, have suggested polyphyletic origins for Munida and the paraphyly of Munididae. Here, we use an integrative approach based on multi-locus phylogenies (two mito­ chondrial and three nuclear markers) paired with 120 morphological characters, to resolve taxonomic and evolutionary relationships within Munididae. Our study covers ~60% of the family’s known diversity (over 800 specimens of 291 species belonging to 19 of the 21 genera collected from the Atlantic, Indian and Pacific oceans). Using this information, we confirm the validity of most genera, proposing new ones in cases where the genetic analyses are compatible with morphological characters. Four well-defined munidid clades were recovered, suggesting that new genera should be erected in the currently recognised Munididae (three for the genus Agononida and eleven in Munida), and the genus Grimothea is resurrected. A key to all genera of the family is presented. Molecular clock estimates and ancestral biogeographic area recon­ structions complement the taxonomic profiles and suggest some explosive diversification within Munididae during the Cretaceous and the Palaeogene. Further anagenetic events and narrow sympatry accounting for changes in distribution indicate a more limited dispersal capacity than previously considered. Our study unravels how diversification may occur in deep waters and further highlights the importance of the integrative approach in accurately delineating species in understanding the history of a family and the factors driving the evolution.

CALSUB, KANACONO, KANADEEP, MAINBAZA, MUSORSTOM 4, MUSORSTOM 8, SANTO 2006, SMCB, SMIB 5, TERRASSES

Munida vassilyi sp.n. and M. hastata sp.n. are described from Kei Islands, Indonesia. Munida vassilyi sp.n. is morphologically related to M. runcinata, from New Caledonia, Vanuatu, Wallis and Futuna, Fiji and Tonga, whereas M. hastata sp.n. is more similar to M. aurantiaca from Papua – New Guinea. Pairwise genetic distances estimated using the COI and 16S rRNA gene fragments indicated high levels of sequence divergence between each new species and their most closely related allies.

KARUBAR

Munida vassilyi sp.n. and M. hastata sp.n. are described from Kei Islands, Indonesia. Munida vassilyi sp.n. is morphologically related to M. runcinata, from New Caledonia, Vanuatu, Wallis and Futuna, Fiji and Tonga, whereas M. hastata sp.n. is more similar to M. aurantiaca from Papua – New Guinea. Pairwise genetic distances estimated using the COI and 16S rRNA gene fragments indicated high levels of sequence divergence between each new species and their most closely related allies.

KARUBAR

Nephropidae collected by expeditions to several localities in the Indian and West Pacific coeans have been examined. One species of Acathacaris, five species of Metanephrops and eight species of Pephropsis have been identified. In addiation, a new species of Metanephrops (M. mozambicus) and two new species of Nephropsis (N. acanthura and N. sulcata) are described. A revision of the genus Nephropsis in the Indian and Pacific oceans is also provided.

BIOCAL, BIOGEOCAL, CORINDON 2, Restricted, MD28 (SAFARI II), MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 5

Lithodes megacantha, a new species from the French Polynesia, in the Central Pacific, is described and illustrated. The species is caracterised by the presence of very long spines on the carapace and walking legs. The species is closely related to L. longispina Sakai, 1971, from Japan.

SMCB

Galatheid crustaceans of the genus Munida collected in several localities in French Polynesia have been studied. The collection contains 14 species, all of them here described a new: Munida amathea, M ducoussoi, M.evarne, M.hystrix, M.lenticularis, M. longicheles, M. ocellata, M. pasithea, M.plexaura, M. polynoe, M.profunda, M.pulchra, M. rubella, and M.rubrovata. An identification key for all these species is provided.

SMCB

In order to clarify the systematic status of Munida japonica Stimpson, 1858, which has been mixed with several other species constituting a complex, a neotype of this species from Kagoshima, Japan, is selected and described. Examination of the type materials of M. heteracantha Ortmann, 1892, M. semoni Ortmann, 1894 (previously merged with M. heteracantha) and M. honshuensis Benedict, 1902 (previously considered synonymous with M. japonica), discloses that they are valid species. Comparison of these species with numerous specimens from the Philippines, Indonesia, Japan, and the western Indian Ocean yields 13 new relatives species to be described.

BIOCAL, CORINDON 2, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3

Fifteen species of galatheid crustaceans belonging to the genus Munida Leach, 1820 are reported from the Philippines and Indonesia. Six of these species are described as new : M. analoga, M. gilii, M. minuta, M. parvula, M. pusiola and M. sacksi.

CORINDON 2, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4

Galatheid crustaceans of the genus Paramunida Baba, 1988, collected in the Philippines, Indonesia and New Caledonia, have been studied. The collection contains 12 species, seven of which are described as new : P. belone, P. evexa, P. pictura, P. polita, P. pronoe, P. stichas, and P. thalie. An identification key for all of the species of the genus is provided.

BIOCAL, CHALCAL 1, CHALCAL 2, CORINDON 2, KARUBAR, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, SMIB 6, VOLSMAR

A large collection of species of the genus Munida has been examined and found to contain 56 undescribed species. The specimens examined were caught mainly off New Caledonia, Chesterfield Islands, Loyalty Islands, Matthew and Hunter Islands. Several samples from Kiribati, the Philippines and Indonesia have also been included. The specimens were collected between 6 and 2 049 m. Some species previously known in the area (Af. Gracilis, M. haswelli, M. microps, M. spinicordata and M. tubercidata) have been illustrated. These results point up the high diversity of this genus in the region and the importance of several characters in species identification (e.g., size and number of lateral spines on the carapace, ornamentation of the thoracic sternites, size of antennular and antennal spines, colour pattern).

AZTEQUE, BATHUS 3, BIOCAL, BIOGEOCAL, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, CORINDON 2, LAGON, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, SMIB 1, SMIB 2, SMIB 3, SMIB 4, SMIB 5, SMIB 6, SMIB 8, VAUBAN 1978-1979, VOLSMAR

BATHUS 1, BATHUS 4, BERYX 11, HALIPRO 1, MUSORSTOM 4

MUSORSTOM 7

Twenty six species of gaiatheid crustaceans belonging to the genera Agononida Baba & de Saint Laurent, 1995 and Munida Leach, 1820, were caught off the Molucca archipelago, during the KARUBAR Cruise (October-November, 1991). Three species are described as new: A. emphereia. M. compacta and M. punctata.

CORINDON 2, KARUBAR, MUSORSTOM 1, MUSORSTOM 2

A new genus, Crosnierita is established for three species of galatheid, crustaceans. C. dicata n.sp., Minida urizaeu Macpherson, 1994 ans M.yante Macpherson, 1994, the latter two having been transfered to the genus Agononida. The new genus is characterized by the abscence of male pleopods on the firt abdominal segment, the frontal margin deeply concave, the lateral margin of the basal antennular segment bearing two spines in addition to the distal spines, the third and fourth segments of the antennal peduncle reduced in size and the merus of the third maxilliped very short. All these characters suggest that the new genus approaches Bathymunida Balss, 1914 and its relatives.

MUSORSTOM 6, MUSORSTOM 8

Galatheid crustaceans of the genera Agononida Baba & de Saint Laurent, 1996 and Munida Leach, 1820 collected in Vanuatu, during the MUSORSTOM 8 cruise (September-October, 1994) have been studied. The collection contains 8 species of the genus Agononida and 25 belonging to the genus Munida. Two species are described as new: A. alisae and M. congesta. A. alisae, close to A. callirhoe (Macpherson, 1994), can be distinguished easily by the spines of the carapace and the antennal peduncle. M. congesta is close to M. miliaris Henderson, 1855, but is distinguished by the shape and the spines of the chelipeds.

MUSORSTOM 8

MUSORSTOM 9

A new galatheid genus, Raymunida, is established for two known species, Munida elegantissima de Man, 1902, and M. bellior Miyake and Baba, 1967, and one new species, R. cagnetei from the Marquesas Islands (French Polynesia, Pacific Ocean). This new genus is easily distinguished from the genus Munida Leach, 1820, and other galatheid genera by the following combination of characters: (1) the presence of epipods on first, second, and third pereiopods; (2) one spine on the frontal margin between supraocular and anterolateral spines; (3) one distal spine on the flexor margin of the carpus of the third maxilliped; (4) the merus of the second pereiopod clearly more slender than those of third and fourth pereiopods; and (5) the presence of several long marginal spines on the endopod of the uropods. Raymunida cagnetei, new species and type species of the genus, is clearly distinguishable from the other species of the genus by the colour pattern, the presence of long setae on the carapace and abdomen, the length of the propodus of the walking legs, and the number of striae on the abdominal somites.

MUSORSTOM 9

Six species of litholid crabs from New Caledonia, Vanuatu, Fiji and French Polynesia are studied. Two new species, Paralomis arae n. sp. and P. dawsoni n. sp., are described. Four other species, Lithodes richeri, Neolithodes brodiei, N. nipponensis and Neolithodes sp., are reported fot the first time from these localities. P. arae n. sp. has the carapace and the abdomen surfaces covered with small granules of various size and it is caracterized by the presence of few scattered spines on the gastric region. The walking legs are moderately long, having well-developed spines along dorsal and ventral margins of merus and propodus. The closest species is P. verrilli from the northeastern Pacific (Bering Sea to California), but they are differentiated by the shape and armature of the carapace and the lenght of the dactylus of the walking legs. P. dawsoni n. sp. has the carapace, abdomen and pereipods surfaces covered with clusters of rounded granules of different sizes. This new species is closely related to P. granulosa from the southern coasts of Argentina and Chile. Both species are easily distinguished by the armature of the carapace, scaphocerite and pereipods and the length of the walking legs.

BORDAU 1, MUSORSTOM 10, MUSORSTOM 8, MUSORSTOM 9

The species of the genus Raymunida from the Pacific and Indian oceans are revised using morphological characters and the mitochondrial cytochrome oxidase subunit I sequences. Four new species are described (R. confundens. R. dextralis, R. erythrina, and R. insulata), and the status of R. bellior and R. elegantissima are revised. The species of Raymunida can be identified by subtle morphological characters, which match differences in mitochondrial nucleotide sequences. Therefore. the sequence divergences confirm the specific and phylogenetic value of some morphological characters (e.g., length of the mesial spine on the basal antennal segment, length of the walking legs). Furthermore. they confirm the importance of the color pattern as a diagnostic character. The widespread species (R. elegantissima), known from the Philippines to Fiji, shows minimal divergence between specimens from different localities (maximum of 3 nucleotide differences or 0.2% mean divergence). The phylogenetic reconstruction agreed with the monophyletic condition of Raymunida and its differentiation with respect to the genus Munida (in which Raymunida species had previously been included) and Agononida.

BATHUS 3, BIOCAL, CHALCAL 1, HALIPRO 1, LAGON, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, SMIB 8

We studied species of the genus Munida Leach collected during several cruises carried out off the Reunion and Aldabra Islands (western Indian Ocean) and Crozet, Saint Paul and New Amsterdam Islands (southern Indian Ocean). Four new species (M. foresti, M. muscae, M. shaula, and M. spicae) are described and illustrated and the taxonomic position of additional material from the John Murray Expedition is also discussed. A key to the species of the genus Munida from the western and southern Indian Ocean is also included.

BENTHEDI, MD08 (BENTHOS), MD30 (BIOMASS CROZET), MD32 (REUNION), Restricted

Four species of Litholid crabs from the Solomon Islands were collected during the Solomon I cruise carried out off the Solomon Islands. One new species, Paralomis mendagnai, is described and illustrated. Three other species, Neolithodes nipponensis, Paralomis dawsoni and P. haigae, are reported for the first time from these islands. The new species of Paralomis closely resembles P. medipacifica Takeda, 1974, from Midway Islands (Central Pacific) and is characterised by the dorsal surface of the carapace thickly covered with rounded, more or less prominent granules of different sizes. Both species are easily distinguished by the armature of the scaphocerite and pereiopods. A key to the species of the genus Paralomis from the western and central Pacific Ocean is presented.

SALOMON 1

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

Three cryptic species of the genus Munida from New Caledonia, previously identified as M. tuberculata Henderson, 1885, M. notata Macpherson, 1994 and M. clinata Macpherson, 1994, are described and illustrated. The three species are identified by subtle and constant morphological characters, which match clear differences in molecular sequences (16S rDNA and COI genes). The results also confirm the importance of several of these characters (e.g. length of the antennular and antennal spines) in the taxonomy of the genus Munida.

BIOCAL, MUSORSTOM 6, NORFOLK 1, NORFOLK 2

During the cruise BENTHAUS (November 2002) to the Austral Archipelago (French Polynesia), numerous specimens of galatheids belonging to the genera Agononida Baba & de Saint Laurent, 1996, Munida Leach, 1820, Paramunida Baba, 1988 and Raymunida Macpherson & Machordom, 2000 were collected. The present collection comprises four Agononida species, 26 Munida, two Paramunida and one Raymunida. A new genus, Setanida, is described. The specimens from BENTHAUS cruise were caught in 68 stations between 50 and 1300 m. Additional material from French Polynesia has also been considered. The collection contains 17 new species: Agononida aequabilis, A. imitata, A. simillima, Munida antliae, M. apheles, M. arae, M. columbae, M. descensa, M. erugata, M. fasciata, M. fornacis, M. ignea, M. llenasi, M. oblonga, Paramunida spatula, Raymunida limbata and Setanida cristata.

BENTHAUS, BORDAU 2, SMCB

Four new species of the genera Eumunida Smith, 1883 (E. spinosa n. sp.), Munida Leach, 1820 (M. aulakodes n. sp., M. devestiva n. sp.) and Torbenia Baba, 2005 (T. calvata n. sp.) are described and illustrated from specimens collected during recent cruises carried out off New Caledonia. Eumunida spinosa n. sp. has two well developed spines on the anterior border of the fourth thoracic sternite (subgenus Eumunida de Saint-Laurent & Poupin, 1996), the posterior region of the carapace with complete striae, the carapace with two pairs of anterolateral spines, no ventral pad on the propodus of the chelipeds, and two rows of well developed spines on the palm of the cheliped. Munida aulakodes n. sp. is characterized by the presence of three spines on the branchial lateral margins of the carapace, spines on the anterior ridge of the second abdominal somite, and two carinae separated by a furrow, on each lateral part of the seventh thoracic sternite. Munida devestiva n. sp. has a carapace without complete transverse ridges, small eyes, with the corneae barely wider than the eyestalk, and the abdominal segments unarmed. Torbenia calvara n. sp. is easily differentiated from the other species of the genus by the absence of spines on the anterior ridge of the second abdominal segment, and the small size of the first anterolateral spine of the carapace. A new occurrence of the rare species Pseudomunida fragilis Haig, 1979 is also reported.

CHALCAL 2, HALIPRO 2, NORFOLK 2

Three new species of squat lobsters are described and illustrated from specimens collected during recent cruises carried out in the Southwest and Central Pacific. Anoplonida patae n. sp. has a well developed cardiac process, pairs of both epigastric spines and postcervical processes, one or two flexor marginal spines on the mxp 3 merus, and a single distolateral spine on the antennular basal article. Bathymunida avatea n. sp. is characterized by the dorsal surface of the carapace having numerous scale-like ridges, the distomesial spine of the basal article of the antennal peduncle reaching the end of article 2, and the distolateral spine of article 2 reaching the mid-length of article 3. Heteronida clivicola n. sp. has each posterior branchial region of the carapace without a distinct elevation, the gastric process being low and rounded, and the disto lateral margin of antennal article 2 strongly produced, nearly reaching the end of article 3. New records of seven species (Anoplonida inermis, Bathymunida sibogae, Heteronida aspinirostris, Neonida grandis, Onconida modica, O. tropis and Plesionida psyla) also are reported.

BENTHAUS, BORDAU 1, BORDAU 2, MUSORSTOM 7, SALOMON 1, SALOMON 2

Sixty-six species of the genus Munidopsis have been studied using specimens collected during numerous French expeditions carried out in the last decades in the deep-waters of the southwest Indian and southwest Pacific Oceans, between 140 and 4400 m. Twenty-five new species are described, and the diagnoses and illustrations of some relatively rare species (M. africana, M. debilis, M. lenzii, M. moresbyi, M. orcina, M. sinclairi, M. stylirostris and M. wardeni) are provided. The reestablishment of the genus Galacantha is proposed, including the descriptions/diagnoses and a key to all species. The genus contains nine species, including three new species (G. bellis, G. diomedeae, G. quiquei n. sp., G. rostrata, G. spinosa, G. subrostrata n. sp., G. subspinosa n. sp., G. trachynotus and G. valdiviae). The number of species collected by station is very small (usually one species), probably related to their low densities. However, in some samples, as many as five species have been found. The highest number of species have been observed in the Banda Sea (Indonesia) and Solomon Islands. The new records of some species greatly extend the previously known distribution range of the species.

BATHUS 1, BATHUS 2, BENTHAUS, BENTHEDI, BIOCAL, BIOGEOCAL, BOA0, BOA1, BORDAU 1, CHALCAL 2, CORINDON 2, Restricted, Restricted, Restricted, Restricted, Restricted, Restricted, Restricted, HALIPRO 2, KARUBAR, MD20 (SAFARI), MD32 (REUNION), MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 4, MUSORSTOM 7, MUSORSTOM 8, NORFOLK 2, PANGLAO 2005, SALOMON 1, SALOMON 2, VOLSMAR, Restricted, Restricted

Seven species of Lithodid crabs were collected during cruises off Taiwan and Guam. One new species, Lithodes paulayi is described and illustrated. Neolithodes nipponensis, Lithodes sp., Paralomis arae, P. dofleini and P. truncatispinosa are reported from these islands for the first time, extending the distributional range in each case. Lithodes paulayi closely resembles L. longispina Sakai, 1971, from off Japan and the central Pacific, but can be differentiated by the branchial region possessing two long dorsal spines and only one long marginal spine, whereas L. longispina has only one long dorsal spine, situated at level of cardiac spines, and two long marginal spines. The description of a juvenile of P. arae Macpherson, 2001, is also included.

TAIWAN 2001, TAIWAN 2002

Two new species of squat lobsters are described. Agononida rubrizonata n. sp. from Taiwan, Vanuatu, New Caledonia, Queensland and New South Wales, is distinguished from A. incerta (Henderson, 1888) by the male telson with a strong anterolateral process and different color pattern, although females of the two species are not morphologically separable. In order to establish the taxonomic status of A. incerta originally described from a female holotype, topotypic material is described. Paramunida leptotes n. sp. from the Izu Islands off Honshu, Japan, the Kyushu-Palau Ridge, off Amami-oshima of the Ryukyus, and Taiwan is distinguished from P. proxima (Henderson, 1885) by the absence instead of presence of a spine on the posterior ridge of the fourth abdominal somite and much narrower and more elongate third antennal segment that is at least 1.5 times longer than instead of as long as broad and about half instead of two-thirds as broad as the article 2.

BATHUS 1, CORAIL 2, KARUBAR, MUSORSTOM 10, MUSORSTOM 6, SANTO 2006

Seven new species of the genera Munida Leach, 1820 (M. acola n. sp., M. clevai n. sp., M. jubata n. sp., M. mica n. sp., M. pauxilla n. sp. and M. squarrosa n. sp.) and Raymunida Macpherson & Machordom, 2000 (R. vittata n. sp.) are described and illustrated from specimens collected during recent cruises carried out off Vanuatu. Munida acola n. sp. has the second abdominal somite unarmed, distal spines of the antennular peduncle unequal in size, and the P2-P4 dactyli with spines along the entire ventral border. Munida clevai n. sp. has small eyes, and spines on the anterior ridge of second abdominal somite. Munida jubata n. sp. is characterized by the presence of spines on the second abdominal somite, and unequally sized distal spines of antennular peduncle. Munida mica n. sp. and M. pauxilla n. sp. have the frontal margin oblique, abdominal somites Unarmed, and distal spines of antennular peduncle of different size. Munida squarrosa n. sp. has the second abdominal segment with spines, and the distal half of the ventral border of P2-P4 dactyli unarmed. Raymunida vittata n. sp. belongs to a group of species having the mesial spine of first antennal segment not reaching the end of the basal segment of antennular peduncle, and mero-carpal articulation of P4 nearly reaching the frontal margin of the carapace.

BOA1, LIFOU 2000, SANTO 2006

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 revision of the genus Sadayoshia Baba, 1969 (type species: S. miyakei Baba, 1969) is carried out based on more than 460 specimens from numerous localities in the Indo-Pacific, revealing the existence of seven species. Sadayoshia edwardsii (Miers, 1884) is redescribed using material collected near the type locality (SW Indian Ocean) and from numerous localities from the Indian and Pacific Oceans. The three previously described species (S. acroporae, S. balica, and S. miyakei) proved to be valid species. Four additional species are described here as new to science: S. latisternata n. sp. from French Polynesia, Loyalty Islands and Mauritius Island; S. lipkei n. sp. from French Polynesia, Solomon Islands, Vanuatu, New Caledonia, Loyalty Islands and Chesterfield Islands; S. inermis n. sp. from Solomon Islands, Vanuatu and New Caledonia; and S. tenuirostris n. sp. from Japan, South China Sea, Palau Islands, Philippines, Indonesia, Solomon Islands, Vanuatu and New Caledonia.

BENTHAUS, CHALCAL 1, CORAIL 2, LAGON, LIFOU 2000, MONTROUZIER, NORFOLK 2, PALEO-SURPRISE, PANGLAO 2004, SALOMON 1, SANTO 2006, SMIB 5

ATIMO VATAE

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.

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

Careful examination of the morphology of recently obtained specimens as well as previously reported specimens of the genus Sadayoshia, initiated by unpublished molecular data that suggest the existence of several different species, led us to describe six new species. The species are very similar to one another and distinguished by very slight morphological differences. Some of the characters that were previously considered as intraspecifically variable in some species, proved to be valid for species discrimination. A dichotomous key to all species of the genus is provided.

CHALCAL 1, CORAIL 2, LAGON, LIFOU 2000, SALOMON 1, SANTO 2006

ATIMO VATAE, CORAIL 2, LAGON, LIFOU 2000, MIRIKY, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 7, NORFOLK 2, PANGLAO 2004, SALOMON 1, SANTO 2006, SMIB 5

During the cruise TARASOC (September and October 2009) to the Tarava Seamounts, and Tuamotu and Society Archipelagos (French Polynesia), numerous specimens of squat lobsters belonging to the family Munididae (Agononida Baba & de Saint Laurent, 1996, Babamunida Cabezas et al., 2008, Bathymunida Balss, 1914, Heteronida Baba & de Saint Laurent, 1996, Munida Leach, 1820, Onconida Baba & de Saint Laurent, 1996, Paramunida Baba, 1988) and the family Eumunididae (Eumunida Smith, 1883) were collected. The study of these specimens revealed the presence of 27 species. Three species are described as new: Bathymunida corniculata n. sp., Munida atarapa n. sp. and M. rona n. sp.

TARASOC

The genus Galathea is one of the most speciose and unwieldy groups in the family Galatheidae. The examination of more than 9000 specimens of 144 species collected in the Indian and Pacific Oceans using morphological and molecular characters, has revealed the existence of 92 new species. The specimens examined during this study were obtained by various French expeditions supplemented by other collections from various sources, and including the type specimens of some previously described species. Most of the new species are distinguished by subtle but constant morphological differences, which are in agreement with molecular divergences of the mitochondrial markers COI and/or 16S rRNA. Here, we describe and illustrate the new species and redescribe some previously described species for which earlier accounts are not sufficiently detailed for modern standards. Furthermore we include a dichotomous identification key to all species in the genus from the Indian and Pacific Oceans.

ATIMO VATAE, BATHUS 1, BATHUS 2, BATHUS 3, BATHUS 4, BENTHAUS, BENTHEDI, BIOCAL, BIOPAPUA, BOA0, BOA1, BORDAU 1, BORDAU 2, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, Restricted, CORINDON 2, Restricted, Restricted, EBISCO, HALIPRO 1, KARUBAR, LAGON, LIFOU 2000, MAINBAZA, MD32 (REUNION), MIRIKY, MONTROUZIER, MUSORSTOM 1, MUSORSTOM 10, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 5, MUSORSTOM 6, MUSORSTOM 7, MUSORSTOM 8, MUSORSTOM 9, NORFOLK 1, NORFOLK 2, PAKAIHI I TE MOANA, PALEO-SURPRISE, PANGLAO 2004, PAPUA NIUGINI, Restricted, RAPA 2002, Restricted, SALOMON 1, SALOMON 2, SANTO 2006, SMIB 5, SMIB 8, Restricted, Restricted, TERRASSES

ATIMO VATAE, BENTHEDI, MAINBAZA, MD08 (BENTHOS), MD32 (REUNION), MIRIKY

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.

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

More than 5000 specimens of squat lobsters belonging to the families Munididae and Munidopsidae were collected during four cruises along the coasts of Papua New Guinea. The study of these specimens revealed the presence of 13 new species (one Babamunida, one Crosnierita, eight Munida, one Paramunida and two Munidopsis). Overall, 109 species of Munididae and 37 of Munidopsidae are recognized. We include the records of all species, describing and illustrating the new species. Furthermore, we provide some new data on the colour patterns for some species. We have also included molecular data from two mitochondrial markers (16S rRNA and COI) to support the taxonomic status of different new species.

BIOPAPUA, EBISCO, EXBODI, KANADEEP, KAVIENG 2014, MADEEP, PAPUA NIUGINI, SALOMONBOA 3

ATIMO VATAE, BIOMAGLO, MAINBAZA, MIRIKY, Walters Shoal

Specimens of munidid squat lobsters belonging to the genera Heteronida Baba & de Saint Laurent, 1996 and Torbenella Baba, 2008 were collected in scientific expeditions made by several French cruises along the southwestern Pacific. These specimens were identified as two species (one new) of Heteronida and six species (four new) of Torbenella. The present paper provides systematic accounts of the five new species, along with new locality records of known species shown by this material and color information where available. Molecular data is provided to support the systematic status of each new species. A key to species for each of the genera is also presented.

BIOPAPUA, BORDAU 2, EBISCO, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, MUSORSTOM 7, PAPUA NIUGINI, SPANBIOS

Specimens of squat lobsters belonging to the family MunididaeAhyong et al., 2010, representing the genera Garymunida Macpherson & Baba, 2022, Trapezionida Macpherson & Baba, 2022 and Typhlonida Macpherson & Baba, 2022, were collected during several cruises around New Caledonia and Papua New Guinea, Southwest Pacific. The integrative study of these specimens revealed the presence of one new species in Garymunida , five in Trapezionida and one in Typhlonida . We describe and illustrate these new species, providing some new data on the taxonomy of several rare or scarcely studied species of Trapezionida . Molecular data from different markers (mitochondrial and nuclear) was also included, based on data availability, to support the taxonomic status of different species. Finally, a key to species for each genus is also provided.

BIOPAPUA, EBISCO, EXBODI, KANACONO, KANADEEP, KAVIENG 2014, MADEEP, NORFOLK 2, PAPUA NIUGINI, SPANBIOS, TARASOC, TERRASSES

Specimens of squat lobsters belonging to the family Galatheidae, representing the genera Galathea and Nanogalathea, were collected during several cruises carried out in New Caledonia, Papua New Guinea, the Philippines and Phoenix Islands. The study of these specimens integrating molecular and morphological data revealed the presence of eight new species in Galathea and one in Nanogalathea. We describe and illustrate these new species. Molecular data from mitochondrial markers were also included to support the taxonomic status of the species. Finally, a key to species for the genus Galathea from the Indian and Pacific Oceans is also provided.

BIOPAPUA, KANACONO, KAVIENG 2014, KOUMAC 2.3, MUSORSTOM 3, MUSORSTOM 8, PAPUA NIUGINI, SPANBIOS

Several species of litholid crabs from the Western Pacific were studied. One new species (Lithodes richeri) from New Caledonia is described. The five other species (Neolithodes vinogradovi, Lithodes turritus, Paralomis segranti, Paralomis haigae and Paralomis sp.) are reported for the first time in the area and their taxonomic position is discussed.

BIOCAL, BIOGEOCAL, MUSORSTOM 3

Squat lobsters have a worldwide distribution and are highly visible crustaceans living in a broad range of habitats. In this study, partial sequences of two mitochondrial DNA genes (16S rRNA and COI) and a nuclear gene (H3) were obtained for all but one of the known species of the shallow-water genera Sadayoshia (Munididae) and Lauriea, Macrothea and Triodonthea (Galatheidae). Lauriea siagiani appeared to be phylogenetically closer to Triodonthea and Macrothea than to other Lauriea species, suggesting the need for taxonomic re-evaluation of these taxa. All species of Sadayoshia formed a monophyletic group that would have diverged during the Paleogene (around 50 Mya). Our results support the hypothesis that the late Paleogene–Neogene transition was a period of rapid diversification for shallowwater species of both Galatheidae and Munididae in the Indo-Pacific region. This is probably related to high tectonic activity among the Eurasian, Philippine Sea, Indo-Australian and Pacific plates and corresponding changes in distribution of habitats and ocean currents during the late Paleogene. Finally, the tropical south-west Pacific province is identified as a major diversification centre for shallow-water squat lobsters, from where species dispersed to other Pacific and Indian Ocean regions.

ATIMO VATAE, BENTHAUS, CHALCAL 1, CORAIL 2, LAGON, LIFOU 2000, MIRIKY, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 7, SALOMON 1, SANTO 2006, SMIB 5

The primary purpose of DNA-barcoding projects is to generate an efficient expertise and identification tool. This is an important challenge to the taxonomy of the 21st century, as the demand increases and the expert capacity does not. However, identifying specimens using DNA-barcodes requires a preliminary analysis to relate molecular clusters to available scientific names. Through a case study of the genus Eumunida (Decapoda : Eumunididae), we illustrate how naming molecule-based units, and thus providing an accurate DNA-based identification tool, is facilitated by sequencing type specimens. Using both morphological and unlinked molecular markers (COI and 28S genes), we analysed 230 specimens from 12 geographic areas, covering two-thirds of the known diversity of the genus, including type specimens of 13 species. Most hypotheses of species delimitation are validated, as they correspond to molecular units linked to only one taxonomic name (and vice versa). However, a putative cryptic species is also revealed and three entities previously named as distinct species may in fact belong to a single one, and thus need to be synonymised. Our analyses, which integrate the current naming rules, enhance the a-taxonomy of the genus and provide an effective identification tool based on DNA-barcodes. They illustrate the ability of DNA-barcodes, especially when type specimens are included, to pinpoint where a taxonomic revision is needed.

BIOCAL, CHALCAL 1, KARUBAR, LITHIST, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 7, NORFOLK 1, NORFOLK 2, SALOMON 1, SMCB

BATHUS 1, BORDAU 1, HALIPRO 1, KAVIENG 2014, MUSORSTOM 10, MUSORSTOM 8, PAPUA NIUGINI, SANTO 2006

The genus Munidopsis is one of the most diverse genera within squat lobsters. Here, three new species of Munidopsis, M. cornuata n. sp., M. senticosa n. sp., and M. turgida n. sp., from <500 m off Guadeloupe Island (Caribbean Sea), are fully described and illustrated. Among the Atlantic species of the genus, M. cornuata n. sp. belongs to the group of species having the dorsal surface of the carapace with spines and is most similar to M. robusta (A. Milne-Edwards, 1880), from the Gulf of Mexico and Caribbean Sea. Munidopsis senticosa n. sp. resembles M. barbarae (Boone, 1927) from the Bahamas and the Gulf of Mexico and M. penescabra Pequegnat & Williams 1995, from off Georgia and Gulf of Mexico; the three species belong to the group having the carapace covered with sharp spines. Finally, M. turgida n. sp. is characterized by having the dorsal surface of the carapace, abdomen and pereiopods covered by granules; and resembles M. granulens Mayo, 1972, from NW Caribbean Sea. Apart from the morphological evidence, the analysis of mitochondrial genes (COI and 16S) supports establishing these new species, showing very high genetic divergences compared to their congeners (from 14.5 to 17% for COI, and 7.7 to 12.8% for 16S data).

KARUBENTHOS 2

ATIMO VATAE, BENTHAUS, BIOMAGLO, BIOPAPUA, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBAR, KAVIENG 2014, KOUMAC 2.3, LAGON, LIFOU 2000, MD08 (BENTHOS), MD32 (REUNION), MONTROUZIER, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, PAKAIHI I TE MOANA, PALEO-SURPRISE, PAPUA NIUGINI, RAPA 2002, SANTO 2006, TARASOC, Walters Shoal

KAVIENG 2014, LAGON, LIFOU 2000, PAPUA NIUGINI, SANTO 2006

Abstract During two deep-sea expeditions off the island of Guadeloupe, French West Indies, several specimens belonging to MunidaLeach, 1820 and MunidopsisWhiteaves, 1874 (Galatheoidea) were collected. Further study, integrating morphological and molecular data, indicated that some of the specimens belonged to three undescribed species, one to Munida and two to Munidopsis. Munida anteaen. sp. is morphologically closely related to the Atlantic species M. microphthalma A. Milne-Edwards, 1880. Both species can be easily distinguished morphologically and represent independent evolutionary lineages. The closest relative to Munidopsis balconin. sp. is M. glabraPequegnat & Williams, 1995 from the Gulf of Mexico. They can be distinguished by the armature of the carapace and pereiopods, among other differences. Munidopsis pholidotan. sp. is sister to M. squamosa (A. Milne-Edwards, 1880) and both are considered cryptic species, distinguished only by molecular characters and subtle morphological differences like the number of epipodites. Our phylogenetic results show some monophyletic groups within Munidopsis and Munida, and the existence of morphological convergences.

IRPM (ex SMCB) Guadeloupe, KARUBENTHOS 2

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.

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

The taxonomy of Munida Leach, 1820 from the north-eastern Atlantic and Mediterranean Sea was studied using a comparative analysis of morphological characters and molecular markers (mitochondrial and nuclear). Generalized Mixed Yule Coalescence and the Poisson tree process models were used to delimit two groups of closely related species associated with uncertain nomenclature and taxonomic status: (1) Munida intermedia A. Milne Edwards & Bouvier, 1899, M. rugosa (Fabricius, 1775), M. sarsi Huus, 1935 and M. tenuimana Sars, 1872 and (2) M. rutllanti Zariquiey-Álvarez, 1952 and M. speciosa von Martens, 1878. We found that M. tenuimana is restricted to northern Atlantic waters (north of approx. 48° N), while Mediterranean and Bay of Biscay specimens previously assigned to this taxon actually belong to a different species, indicating that the name Munida perarmata A. Milne Edwards & Bouvier, 1894 should be resurrected. Furthermore, M. rutllanti is shown to be a junior synonym of M. speciosa, a species that has thus far only been reported along western Africa. In addition, three species are re-described and a key to European Munida is provided. The validity of the morphological characters used to distinguish the different species is discussed. Phylogenetic analyses revealed three independent lineages with unsolved relationships among them, including high genetic distances for some species. These findings indicate highly divergent lineages of the European Munida and several events of colonization along the eastern Atlantic.

GUYANE 2014

The genus Phylladiorhynchus Baba, 1969 currently contains 11 species, all occurring in the shallow waters and on the continental shelf of the Indian and Pacific oceans. Recent expeditions in these oceans have resulted in the collection of numerous new specimens in need of analysis. We have studied this material using an integrative approach analysing both morphological and molecular (COI and 16S) characters. We describe 41 new species and resurrect three old names: P. integrus (Benedict, 1902) and P. lenzi (Rathbun, 1907), previously synonymized with P. pusillus (Henderson, 1885), and P. serrirostris (Melin, 1939), previously synonymized with P. integrirostris (Dana, 1852). Most species of the genus are described and illustrated. Some species are barely discernible on the basis of morphological characters but are highly divergent genetically. Species of Phylladiorhynchus are mainly distinguishable by the number of epigastric spines and lateral spines of the carapace, the shape and the armature of the rostrum, the number and pattern of the ridges on the carapace and pleon, the shape of thoracic sternite 3 and the armature of the P2–4 dactyli. A dichotomous identification key to all species is provided.

ATIMO VATAE, BENTHAUS, BIOMAGLO, BIOPAPUA, CALSUB, CHALCAL 1, CHALCAL 2, CORAIL 2, EBISCO, EXBODI, KANACONO, KANADEEP, KARUBAR, KAVIENG 2014, KOUMAC 2.1, KOUMAC 2.3, LAGON, LIFOU 2000, MD08 (BENTHOS), MD32 (REUNION), MONTROUZIER, MUSORSTOM 1, MUSORSTOM 2, MUSORSTOM 3, MUSORSTOM 4, MUSORSTOM 6, MUSORSTOM 8, MUSORSTOM 9, PAKAIHI I TE MOANA, PALEO-SURPRISE, PAPUA NIUGINI, RAPA 2002, SANTO 2006, TARASOC, Walters Shoal

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.

BATHUS 3, BERYX 11, BIOGEOCAL, BIOMAGLO, BIOPAPUA, BOA1, BORDAU 2, CHALCAL 2, Restricted, 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, Restricted, TARASOC, VOLSMAR

This study was carried out to test the hypothesis that benthic communities on seamounts are distinct from those of other deep-sea habitats at comparable depths. Analysis of the squat lobster fauna of deep-sea habitats in the Southwestern Pacific revealed that the species composition of assemblages on seamounts was not statistically dissimilar from assemblages on slope and plateau habitat at comparable depths. However, compositional differences were observed between seamount and rise and ridge habitat. Differences in assemblage composition between seamount and ridge habitat were statistically significant for two of the four ridge systems examined. Assemblages on seamounts that were distinct from non-seamount ridge habitat were typically dominated by small-bodied species with an abbreviated larval stage. Various environmental variables were correlated with the observed assemblage patterns observed; depth-related variables may account for differences between seamount and rise assemblages, whilst differences in POC flux likely play a role in determining the assemblage compositional patterns between seamount and non-seamount ridge habitat. Extensive pre-analysis data treatment was required to ensure that multivariate analyses of assemblage data from seamount and non-seamount habitats were robust. Our results confirm the findings of recent studies that found no compositional differences in assemblages from seamount and slope habitats, and support the idea that dissimilarity between seamount assemblages on different ridge systems increases with geographic distance. Further research will be required before the generality of these findings can be confirmed.

BOA0, BOA1, BORDAU 1, BORDAU 2, MUSORSTOM 10, MUSORSTOM 8, SALOMON 1, SALOMON 2, SALOMONBOA 3, SANTO 2006

Previous studies have suggested that the high diversity associated with the Norfolk seamounts (Southwest Pacific) could reflect endemism resulting from limited dispersal due to hydrological phenomena. Crustaceans of the family Galatheidae are thoroughly studied in the New Caledonia economic zone permitting the analysis of species distribution pattern between the New Caledonia slope and Norfolk ridge seamounts. This analysis has shown that, qualitatively, the same species are sampled on seamounts and on the New Caledonia slope. Local endemism was never detected. However, on each seamount, and therefore on a small surface, a very high number of species are usually sampled, suggesting that seamounts are biodiversity hot spots. Then, to evaluate whether the seamounts constitute patches of isolated habitat, we explore the pattern of genetic diversity within several species of crustaceans and gastropods. Analysis of the intra-specific genetic structure using the mitochondrial marker COI reveals that populations of two Galatheidae species (Munida thoe and Munida zebra), polymorphic for this marker, are genetically not structured, both among seamounts and between the seamounts and the island slope. The genetic structure over a similar sampling scheme of two Eumunida species (Chirostylidae, the sister family of Galatheidae) and a planktotrophic gastropod (Sassia remensa) reveals a similar pattern. Population structure is observed only in Nassaria problematica, a non-planktotrophic gastropod with limited larvae dispersal. Thus, the limitation of gene flow between seamounts appears to be observed only for species with limited dispersal abilities. Our results suggest that the Norfolk seamounts rather than functioning as areas of endemism, instead, may be highly productive zones that can support numerous species in small areas.

NORFOLK 1, NORFOLK 2