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.     

Phylogeny of the radula-less dorids (Mollusca, Nudibranchia), with the description of a new genus and a new family

This paper studies the phylogenetic relationships of the nudibranch dorids that lack a radula. Numerous specimens belonging to 29 different species, representing all genera of this group and other related taxa, were examined anatomically. Details of the foregut were examined with SEM. From this anatomical study a total of 62 characters were considered. These characters have been polarized using the genus Berthella as the outgroup. Eight species of dorids with a radula and the genus Armina have been also included in the analysis for comparative purposes. The phylogeny obtained supports the hypothesis that the radula has been lost once in the Doridina and that the radula-less dorids are a monophyletic group. Cryptobranchia is monophyletic when the radula-less dorids are included. The new genus Mandelia , introduced on the basis of a new species from South Africa, is the sister group of the rest of the radula-less dorids, and is described as a new family, Mandeliidae. The radula-less dorids (currently placed in a separate superfamily) actually constitute an internal branch of other cryptobranch dorids. Phyllidia has no synapomorphies that distinguish if from Fryeria , which has one autoapomorphy, the ventral position of the anus. Therefore, both genera are regarded as synonyms. The evolution of several characters among the radula-less dorids is discussed, and the present phylogeny is compared with prior studies.     

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 taxonomy and biology of further aeolidacean and arminacean nudibranch molluscs with symbiotic zooxanthellae

The occurrence of symbiotic zooxanthellae in further aeolid and arminacean nudibranch molluscs is described for the first time. The aeolid Aeolidiopsis ransoni Pruvot-Fol is redescribed, and a new species of Aeolidiopsis , also feeding on the colonial zoantharian Palythoa , is described. Both have symbiotic zooxanthellae. The taxonomy of the family Aeolidiidae is discussed and the genus Berghia Trinchese, 1877 is considered a synonym of Spurilla Bergh, 1864. Spurilla major (Eliot, 1903) and a new species of Spurilla are reported to have zooxanthellae while another new species of Spurilla is without zooxanthellae. The glaucid aeolid Pteraeolidia ianthina (Angas) is shown to have symbiotic zooxanthellae, as is the arminacean Doridomorpha gardineri Eliot, which is reported to feed on the alcyonarian blue coral, Heliopora. In all cases, the morphological adaptations developed for this symbiosis are described. Further notes on the Porites-fetding arminacean Pinufius rebus Marcus & Marcus and the aeolid Phestilla lugubris (Bergh) are included and a facultative symbiosis with zooxanthellae is suggested for the latter. The tion of symbiosis with zooxanthellae within nudibranchs is discussed and it is suggested that the relationship has evolved independently on several occasions.     

Two new species of nudibranchiate molluscs from the west coast of North America, with a revision of the family Cuthonidae

Two species of nudibranch molluscs are described from the northeastern Pacific Ocean on the west coast of North America. These are: a new aeolid species of Cuthona Alder & Hancock, 1855 (family Cuthonidae) from the Oregonian marine zoogeographical province and a new dorid species of Acanthodoris Gray, 1850 (family Onchidorididae) from the Panamic province in the Gulf of California. The internal anatomy and external features of each species are compared with related species. Differences in structure of the radula, reproductive system and other morphological aspects are described. A revision of the family Cuthonidae is included. Evidence is presented to include the genera Trinchesia Ihering, 1879, and Precuthona Odhner, 1929, within the genus Cuthona. Cuthona alpha Baba & Hamatani, 1963, is synonymized with Catriona columbiana (O'Donoghue, 1922). We consider the New World Cuthonidae to be composed of the following five genera: Catriona Winckworth, 1941; Cuthona Alder & Hancock, 1855; Embletonia Alder & Hancock, 1851; Tenellia Costa, 1877; and Tergipes Cuvier, 1805.     

Systematic revision of Jorunna Bergh, 1876 (Nudibranchia: Discodorididae) with a morphological phylogenetic analysis

The genus Jorunna is characterized by a dorsum covered withcaryophyllidia, a prostate with two sections, a penis usuallyunarmed but occasionally armed with hooks, a copulatory spine,the presence of an accessory gland and a labial cuticle smoothor armed with jaw elements. The examination of 216 non-typespecimens, 30 types, and a review of the literature show thatthere are 16 valid species of the genus Jorunna: J. tomentosa(Cuvier, 1804); J. funebris (Kelaart, 1859); J. pantherinaAngas,1864; J. rubescens (Bergh, 1876); J. labialis (Eliot, 1908);J. parva (Baba, 1938); J. spazzola (Marcus, 1955); J. hartleyi(Burn, 1958); J. alisonaeMarcus, 1976; J. lemchei (Marcus, 1976);J. evansi (Eliot, 1906); J. pardusBehrens & Henderson, 1981;J.ramicolaMiller, 1996 and J. onubensis Cervera, García-Gómez& García, 1986. In addition, two new species fromthe Eastern Pacific are described: J. osae n. sp. and J. tempisquensisn. sp. We propose two new combinations: Jorunna parva and J.evansi. New records for the genus Jorunna are provided fromItaly, Algeria, Seychelles, Madagascar, Thailand, Marshall Islands,New Caledonia, Île de la Réunion, Sudan, PapuaNew Guinea, Indonesia, Panama, Costa Rica, Bahamas, and SouthernMexico. We present the first preliminary phylogenetic analysisof this cryptobranch dorid genus, based on morphological anatomicaldata, and discuss the biogeography and evolution of severalcharacters in this group. The phylogeny supports the hypothesisthat the genus Jorunna is a monophyletic group and shows thatKentrodoris is nested within it. (Received 31 December 2004; accepted 10 January 2008)     

细花萤科分类概述与中国种类名录（鞘翅目：郭公总科）

介绍了细花萤科的识别特征,总结了该科分类历史,提供了属级检索表,编制了中国已知种类名录。基于标本检视信息,对一些物种地理分布地进行了补充,包括 Lobonyx guerryi (Pic, 1920)、Prionocerus bicolor Redtenbacher, 1868、P. coeruleipennis Perty,1831、Idgia deusta Fairmaire,1878和I. flavirostris Pascoe,1860。     

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;     

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.     

Aeolid nudibranchs (Gastropoda: Opisthobranchia) of the families Flabellinidae and Eubranchidae from New Zealand waters

Four aeolid species, all newly recorded for New Zealand waters, are described. Three are known species; they are Tularia bractea (Burn) and Eubranchus rubeolus Burn from Australia and Eubranchus agrius Marcus from Chile; the New Zealand specimens show slight variation. The fourth species, Coryphella albomarginata sp. nov. , is distinguished from close relatives by the opaque white band along the margin of the foot, two centrally placed (in relation to the main reproductive ducts) bursae copulatrices and several small, blunt denticles on the outer edge of the lateral teeth of the radula. The families to which these species belong, the Flabellinidae (Coryphella albomarginata, Tularia bractea) and Eubranchidae (Eubranchus agrius, E. rubeolus), are recognized and defined and the constituent genera examined and reduced in number. A new genus, Paracoryphella , and family, the Paracoryphellidae, are created for Coryphella islandica Odhner. The classification of the aeolids is reviewed:Odhner's order Aeolidacea is considered a very satisfactory major category, but his grouping of the families into tribes is discarded on the grounds that the diagnostic character, the position of the anus in relation to the cerata, is too variable within individual families.     

Studies on the morphology and anatomy of the Antarctic nudibranch genera Pseudotritonia Thiele, 1912 and Telarma Odhner, 1934 with a discussion of the family Gharcotiidae Odhner, 1926 (Nudibranchia: Opisthobranchia)

The external morphology and anatomy of the Antarctic nudibranchs Pseudotritonia quadrangularis Thiele, 1912, P. gracilidens Odhner, 1944 and Telarma antarctica Odhner, 1934 are redescribed. Both genera, which were only known by two or one specimen, do not possess a cnidosac, but there is a terminal swelling at the termination of the digestive glandular ramifications in P. gracilidens. This sac is composed of cells with a large vacuole. A glandular stripe on the right side of the body above the genital openings, nephroproct and anal papilla is considered to be a synapomorphy for both genera. The validity of the family Charcotiidae and the affinities to the aeolid genus Notaeolidia Eliot, 1905 and taxa of the Arminacea are discussed.     

On the anatomy and zoogeography of Tritoniella belli Eliot, 1907 (Opisthobranchia,Nudibranchia) and the synonymy of T. sinuata Eliot, 1907

Summary Rich material of the genus Tritoniella (Opisthobranchia, Nudibranchia) from the Atlantic sector of the Antarctic Ocean demonstrates that the features of the internal anatomy are fairly constant in contrast to those of the external morphology and the cuticularized structures (radula and jaws). There are specimens intermediate between the two known species of the genus: T. belli Eliot, 1907 and T. sinuata Eliot, 1907. These specimens either show a combination of features characteristic for T. belli and T. sinuata, or of features which lie in between. Therefore T. sinuata is considered to be synonymous with T. belli. The monotypic genus Tritoniella has a circumpolar distribution with an extension of its range to the Subantarctic (South Georgia).     

Species names and metaphyly: a case study in Discodorididae (Mollusca, Gastropoda, Euthyneura, Nudibranchia, Doridina)

Dayrat, B. & Gosliner, T. M. (2005). Species names and metaphyly: a case study in Discodorididae (Mollusca, Gastropoda, Euthyneura, Nudibranchia, Doridina) —Zoologica Scripta, **, ***–***. Absence of resolution in phylogenetic trees, or metaphyly, is a common phenomenon. It mainly results from the fact that each data set has its own limit and can hardly be expected to reconstruct alone an entire hierarchy. Because metaphyly helps point out which regions of a tree merit further investigation, one should not avoid metaphyly but rather should try to detect it by addressing carefully node reliability. In this paper we explore the implication of metaphyly for species names. We present a phylogenetic analysis of Discodorididae (Mollusca, Gastropoda, Nudibranchia, Doridina), with an emphasis on relationships among species of Discodoris and its traditionally close ‘allies’ such as Peltodoris and Anisodoris. We demonstrate that some species must be transferred to different discodoridid subclades with which they share synapomorphies, but that many species form a metaphyletic group at the base of Discodorididae, and therefore cannot be placed in any taxon of genus level. We demonstrate that the current International Code of Zoological Nomenclature does not allow taxonomists to handle this situation because it requires selecting a taxon name of genus rank for every species binomial. Then we evaluate the results provided by new forms of species names, both in a rank‐based system, such as the current nomenclature, and a rank‐free system. All solutions considered would cause radical changes to the ‘spirit’ of the current ICZN (and, by extension, to the other current codes). In a rank‐free system of nomenclature, such as the PhyloCode, the best result is obtained with an epithet‐based form that does not mention supra‐specific relationships. Under this method, official species names would take the form ‘boholiensis Bergh, 1877’, although page numbers and letters can be added for uniqueness purposes. Taxonomists would then be free to add supra‐specific taxon names in ‘common’ species names, such as Discodorididae boholiensis Bergh, 1877 or simply Discodorididae boholiensis. Here we wish to stimulate discussion of a problem that we believe merits wide debate: absence of resolution in phylogenetic reconstruction and its impact on species nomenclature.     

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)