The morphology and taxonomy of the Antarctic species of Tritonia Cuvier, 1797 (Nudibranchia: Dendronotoidea)

The external morphology and anatomy of the Antarctic nudibranchs Tritonia vorax Odhner, 1926, and Tritonia antarctica Pfeffer in Martens & Pfeffer, 1886, is redescribed in detail and compared with other nominal tritoniids from the Antarctic and Subantarctic waters. Tritonia appendiculata Eliot, 1905, T. challengeriana Eliot, 1907a, non Bergh, 1884, T. chalkngeriana Odhner 1926, non Bergh, 1884, and Marionia cmullata Vicente & Arnaud 1974, non (Couthouy, in Gould 1852), are shown to be synonymous with T. antarctica. Only Tritonia antarctica is a true High Antarctic species, with a distribution around the continental shelf, Antarctic Peninsula and South Georgia. T. vorax is confined to South Georgia and Subantarctic waters.     

THE DISTRIBUTION OF SOME ENDEMIC ANTARCTIC NUDIBRANCHIA

The distribution of six endemic Antarctic nudibranch speciesis described, using both published data and new results fromrecent expeditions to the Atlantic sector of the South PolarSea. Notaeolidia schmekelae Wägele, 1990 is restrictedto the Weddell Sea, and N. gigas Eliot, 1905 to the AntarcticPeninsula and the Scotia Arc. N. depressa Eliot, 1905 is theonly member of the family Notaeolidiidae Odhner, 1926 with acircumpolar distribution. Localities of Pseudotritonia quadrangularisThiele, 1912 and Telarma antarctica Odhner, 1934, are knownaround the Antarctic Continent, whereas Pseudotritonia gracilidensOdhner, 1944 was only collected at the Antarctic Peninsula.The biogeographical divisions, discussed by several authors,do not coincide in all aspects with the distribution patternsof the Nudibranchia. According to my results, the AntarcticPeninsula forms a separate faunal zone, with transitional elementsof the High Antarctic and Subantarctic zone. South Georgia hasno endemic nudibranchs. (Received 30 March 1990; accepted 23 September 1990)     

A phylogenetic analysis and systematic revision of the cryptobranch dorids (Mollusca, Nudibranchia, Anthobranchia)

The phylogenetic relationships of the cryptobranch dorids are studied based on morphological characters of species belonging to all previously described genera. The phylogenetic hypothesis supports the cryptobranch dorids as a monophyletic group. There are two major clades within the Cryptobranchia: the radula‐less dorids (Porostomata), and the radula‐bearing dorids ( Labiostomata new taxon ). Labiostomata consists of those taxa sharing a more recent common ancestor with Actinocyclus than with Mandelia, and includes several monophyletic groups: Actinocyclidae, Chromodorididae, Dorididae and Discodorididae. The traditional group Phanerobranchia is probably paraphyletic. The new classification proposed for the Cryptobranchia addresses concepts of phylogenetic nomenclature, but is in accordance with the rules of the International Code of Zoological Nomenclature. The following genera of cryptobranch dorids are regarded as valid: Doris Linnaeus, 1758, Asteronotus Ehrenberg, 1831, Atagema J. E. Gray, 1850, Jorunna Bergh, 1876, Discodoris Bergh, 1877, Platydoris Bergh, 1877, Thordisa Bergh, 1877, Diaulula Bergh, 1878, Aldisa Bergh, 1878, Rostanga Bergh, 1879, Aphelodoris Bergh, 1879, Halgerda Bergh, 1880, Peltodoris Bergh, 1880, Hoplodoris Bergh, 1880, Paradoris Bergh, 1884, Baptodoris Bergh, 1884, Geitodoris Bergh, 1891, Gargamella Bergh, 1894, Alloiodoris Bergh, 1904, Sclerodoris Eliot, 1904, Otinodoris White, 1948, Taringa Er. Marcus, 1955 , Sebadoris Er. Marcus & Ev. Marcus, 1960, Conualevia Collier & Farmer, 1964, Thorybopus Bouchet, 1977, Goslineria Valdés, 2001, Pharodoris Valdés, 2001, Nophodoris Valdés & Gosliner, 2001. Several genera previously considered as valid are here regarded as synonyms of other names: Doridigitata d’Orbigny, 1839, Doriopsis Pease, 1860, Staurodoris Bergh, 1878, Fracassa Bergh, 1878, Archidoris Bergh, 1878, Anoplodoris Fischer, 1883, Etidoris Ihering, 1886, Phialodoris Bergh, 1889, Montereina MacFarland, 1905, Ctenodoris Eliot, 1907, Carryodoris Vayssière, 1919, Austrodoris Odhner, 1926, Guyonia Risbec, 1928, Erythrodoris Pruvot‐Fol, 1933, Neodoris Baba, 1938, Siraius Er. Marcus, 1955, Tayuva Ev. Marcus & Er. Marcus, 1967, Nuvuca Ev. Marcus & Er. Marcus, 1967, Doriorbis Kay & Young, 1969, Pupsikus Er. Marcus & Ev. Marcus, 1970, Percunas Ev. Marcus, 1970, Verrillia Ortea & Ballesteros, 1981 . The genera Artachaea Bergh, 1882, Carminodoris Bergh, 1889 and Homoiodoris Bergh, 1882 have been poorly described and no type material is known to exist. They are regarded as incertae sedis until more material becomes available. The genus names Xenodoris Odhner in Franc, 1968 and Cryptodoris Ostergaard, 1950 are unavailable within the meaning of the Code. Hexabranchus Ehrenberg, 1831 is not a cryptobranch dorid, as suggested by other authors, because of the lack of a retractile gill. Other nomenclatural and taxonomic problems are discussed, and several type species, neotypes and lectotypes are selected. © 2002 The Linnean Society of London. Zoological Journal of the Linnean Society, 2002, 136 , 535?636.     

A new tritoniid species (Mollusca: Opisthobranchia) from Bouvet Island

Tritoniid sea slugs (Mollusca, Gastropoda, Opisthobranchia) are reported for the first time from Bouvet Island. Tritonia dantarti sp. n. shows morphological and anatomical differences with regard to the two previously known tritoniids reported from Antarctica and Sub-Antarctica, Tritonia vorax (Odhner 1926) and Tritonia challengeriana Bergh, 1884. Regarding the external morphology, T. dantarti sp. n. is characterized by a very bright orange coloration in the dorsum, white dorsal crests, highly ramified dendritic gills (the largest vertically orientated and the rest laterally orientated), and a quadrangular cross section. The radula presents very long, thin lateral teeth and the jaws present mainly unicuspidate, striated denticles. The seminal receptacle is large, pear-shaped and its grey pigmentation differs from the rest of the genital system. The Antarctic species T. challengeriana was also found in waters off Bouvet Island, while the Subantarctic species T. vorax was not found.     

Die Gattung Bathydoris Bergh, 1884 (Gnathodoridacea) im phylogenetischen System der Nudibranchia (Opisthobranchia, Gastropoda)

The genus Bathydoris Bergh, 1884 (Gnathodoridacea) in the phylogenetic system of the Nudibranchia (Opisthobranchiu, Gastropoda) The position of the genus Bathydoris Bergh, 1884 in the phylogenetic system of the Nudibranchia is discussed. Doridoxa Bergh, 1900, a genus which is assigned to the taxon Gnathodoridacea together with the genus Bathydoris, is taken out from this taxon, lacking snapomorphies. Doridoxa is considered to be a sister grou of the Euctenidiacea, with the transrormation of the right digestive gland into a caecum as the only synaomorphy with the latter. The Gnathodoridacea with the one enus Bathydoris is removed from the taxon Doridacea and considered to be the sister group or the latter. Gnathodoridacea and Doridacea form the taxon Euctenidiacea with the synapomorphy “dorsomedial position of anus and nephroproct”.     

ON THE STATUS OF THE GENERIC NAMES OF THE NUDIBRANCH GENERA CATRIONA, CRATENA, HERVIA, RIZZOLIA AND TRINCHESIA

The genus Catriona Winckworth (1941) is synonymous with TrinchesiaPruvot-Fol (1951) but not with Trinchesia von Jhering (1879). It has priority over Trinchesia Pruvot-Fol. The genus Cratena Bergh (1864) is valid and synonymous withRizzolia Trinchese (1877) but not with Hervia Bergh (1871). The genus Hervia Bergh (1871) is synonymous with Facelina Alderand Hancock (1855), but not all species of Hervia can be includedin the latter genus, and these should, therefore, be distributedamong other genera, some of which are listed. (Received 8 October 1954;     

Revision of the Antarctic genus Notaeolidia (Gastropoda, Nudibranchia), with a description of a new species

New material from the Atlantic sector of the Antarctic Ocean allows a revision of the Antarctic genus Notaeolidia Eliot, 1905. One new species (Notaeolidia schmekelae sp.n.) is described. N. depressa Eliot, 1905 and N. gigas Eliot, 1905, which arc poorly known, arc redescribed. N. rufopicta Thiele, 1912, N. robsoni Odhner, 1934, N. subgigas Odhner, 1944, N. alutacea Minichev, 1972 and N. flava Minichev, 1972 are synonymized with N. depressa. N. purpurea Eliot, 1905 is synonymized with N. gigas. The monogeneric family Notaeolidiidae Odhner, 1926. is characterized by the following autapomorphy: "nephroproct in front of the genital apertures". Too little is known to elaborate the phylogenetic position of the family Notaeolidiidae within the cladobranch Nudibranchia.     

Anatomical and taxonomical studies of the Antarctic nudibranchsAustrodoris kerguelenensis (Bergh, 1884) andA. georgiensis n. sp. from the Scotia Sea

During the expedition ANTARTIDA 8611 to the Scotia Sea, organized by the Spanish Oceanographic Institute, several specimens ofAustrodoris were collected. Although nearly all have been identified asAustrodoris kerguelenensis (Bergh, 1884), one of them shows some anatomical features, mainly related to the reproductive system, that allows us to identify this specimen as a new species, which we have namedA. georgiensis. Therefore, with the aim of clarifying the taxonomical value of this species, a comparative study of the anatomy ofA. kerguelenensis andA. georgiensis is presented. Some new data on the diet ofA. kerguelenensis are also presented.     

Systematics and phylogeny of the caryophyllidia-bearing dorids (Mollusca, Nudibranchia), with descriptions of a new genus and four new species from Indo-Pacific deep waters

The phylogenetic relationships of the caryophyllidia-bearing dorids are studied, based on the examination of the type species of all the genera previously described. The phylogenetic hypothesis supports that the caryophyllidia-bearing dorids are a monophyletic group and the sister group of the clade formed by Astemnotus Ehrenberg, 1831 and Halgerda Bergh, 1880. Several genera previously considered as valid or regarded as uncertain are here synonymized: Peronodoris Bergh, 1904, Trippa Bergh, 1877, Phlegmodoris Bergh, 1878, Petelodoris Bergh, 1881, Kentrodoris Bergh, 1876, Audura Bergh, 1878, Centrodoris P. Fischer, 1883, Anisodoris Bergh, 1898, Awuka Er. Marcus, 1955, Rhabdochiia P. Fischer, 1883, Boreodoris Odhner, 1939, Dictyodoris Bergh, 1880, Gravieria Vayssiere, 1912, Aporodoris Ihering, 1886. The following genera are regarded as valid: Astemnotus, Atagema J.E. Gray, 1850, Jorunna Bergh, 1876, Platydoris Bergh, 1877, Diaulula Bergh, 1878, Rostanga Bergh, 1879, Halgerda Bergh, 1880, Baptodoris Bergh, 1884, Gargamella Bergh, 1894, Alloiodoris Bergh, 1904, Sclerodoris Eliot, 1904, Taringa Er. Marcus, 1955, Thorybopus Bouchet, 1977. The new genus Nophodoris is described based on two new species from New Caledonia deep waters. Two additional new species from New Caledonia belonging to the genera Atagema and Gargamella are also described. Nomenclatural and taxonomic problems are discussed, and several type species, neotypes and lectotypes are selected.     

A NEW SPECIES OF RUNCINELLA ODHNER, 1924 (GASTROPODA: OPISTHOBRANCHIA) FROM THE GALAPAGOS ISLANDS

Runcinella thompsoni new species (Gastropoda: Opisthobranchia)is described on the basis of material collected in the GalapagosIslands. This new species differs from R. zelandica Odhner,1924, both in colour, reddish in the former, dark green withwhite freckles in the latter, and radular tooth morphology,mainly the first lateral teeth. The species is also comparedwith other red runcinids both from Atlantic and Pacific localities. (Received 28 October 1991; accepted 4 January 1993)     

THE DISTRIBUTION OF SOME ANTARCTIC NUDIBRANCHS (OPISTHOBRANCHIA)

The circumpolar distribution of the four revised species ofdoridacean nudibranchs: Aegires albus, Bathydoris hodgsoni,B. clavigera and Austrodoris kerguelenensis, is demonstrated,taking into consideration the known data from the literatureand new localities from the Atlantic sector of the Antarctic.A. albus and B. hodgsoni are restricted to the High AntarcticZone. A. kerguelenensis is widely distributed in the High Antarcticand Subantarctic Zone, whereas localities of B. clavigera arerestricted to the High Antarctic Zone and the Atlantic sectorof the Subantarctic Zone. (Received 13 November 1986;     

Descriptions of digeneans from <Emphasis Type="Italic">Sardina pilchardus</Emphasis> (Walbaum) (Clupeidae) off the Algerian coast of the western Mediterranean,with a complete list of its helminth parasites

Five species of digeneans parasitic in the pilchard Sardina pilchardus (Walbaum), a little studied host, from off the Algerian coast of the western Mediterranean are redescribed. These are Parahemiurus merus (Linton, 1910) Manter, 1940, Aphanurus stossichii (Monticelli, 1891) Looss, 1907, Aphanurus virgula Looss, 1907, Lecithaster confusus Odhner, 1905 and Pronoprymna ventricosa (Rudolphi, 1819) Poche, 1926. One of these, A. virgula, is a new record for this host. One other digenean, Hemiurus luehei Odhner, 1905, was also recorded from this host. A complete checklist of the helminth parasites of S. pilchardus throughout its distributional range, comprising 104 host-parasite records of 39 taxa, is presented.     

NORTH ATLANTIC SPURILLID NUDIBRANCHS, WITH A DESCRIPTION OF A NEW SPECIES, SPURILLA COLUMBINA, FROM THE ANDALUSIAN COAST OF SPAIN

The new species Spurilla columbina differs from its Europeancongeners in coloration and the shape of its cerata. Comparativedata derived from S. norvegica (Odhner, 1939), S. coerulescens(Laurillard, 1830) and S. verrucicornis (Costa, 1864) are tabulated. ^* T. E. Thompson died in a car accident 1 January 1990 (Received 10 January 1989; accepted 4 July 1989)     

PHYLOGENY OF THE GENUS ROSTANGA (NUDIBRANCHIA), WITH DESCRIPTIONS OF THREE NEW SPECIES FROM SOUTH AFRICA

Rostanga elandsia sp. nov., Rostanga aureamala sp. nov. andRostanga phepha sp. nov. are characterized by having the radulawith slender innermost lateral teeth, which lack denticles onthe inner side of the cusp and have a single denticle on theouter side. The outermost lateral teeth of these three speciesare elongate, but shorter than in other species of the genus.In addition, R. aureamala is the only species of the genus withrachidian teeth and R. phepha is unique within the genus Rostanga byvirtue of its white coloration with dark spots. A phylogenetic analysis shows that the three new species fromSouth Africa and Rostanga setidens (Odhner, 1939) are the sistergroup of the rest of the genus. The species from Japan and MarshallIslands (North Pacific Ocean) are basal in the sister cladecontaining the other species of Rostanga Bergh, 1879. The tropicalIndo-Pacific species of Rostanga are not monophyletic. The Atlanticand Eastern Pacific species form a monophyletic, derived clade,being the sister group of Rostanga australis Rudman & Avern,1989, which has a narrow range restricted to south eastern Australia.The widespread Indo-Pacific species Rostanga bifurcata Rudman& Avern, 1989, is the sister group of Rostanga dentacus Rudman& Avern, 1989, also widesprad in the tropical western Pacific. This phylogeny suggest s a viariant origin of the Sourth African, Atlantic-EasternPacific, and probably North Pacific species, whereas in thetropical Indo-Pacific most sister speceis are sympatric. (Received 16 May 1999; accepted 31 July 2000)     

Reassessment of the Systematic Status of Miamira Bergh, 1875 and Orodoris Bergh, 1875 (Nudibranchia: Chromodorididae) in Light of Phylogenetic Analysis

The external morphology and anatomy of the opisthobranch gastropodsMiamira sinuata (van Hasselt, 1824) and Orodoris miamiranaBergh, 1875, the type species of the genera Miamira Bergh, 1875and Orodoris Bergh, 1875, and their phylogenetic relationshipsare studied. The phylogeny obtained supports the placement ofM. sinuata and O. miamirana in the genus Ceratosoma J. E. Gray, 1850.Therefore, Miamira and Orodoris become synonyms of the seniorvalid name Ceratosoma. In addition, the family name MiamiridaeBergh, 1891, based on Miamira, is newly recognized as a synonymof Chromodorididae Bergh, 1891. Ceratosoma sinuata and C. miamirana are more closely relatedto the highly derived Ceratosoma alleni than to other membersof the genus. C. miamirana appears to present reversal to theplesiomorphic state in the body shape and has secondarily lostits mantle glands. (Received 5 January 1998; accepted 23 April 1998)