Observations on Australian Glaucidae (Mollusca:Opisthobranchia)

Glaucilla Bergh, 1868 is positively recorded for the first time from eastern Australia, together with Glaucur Forster, 1777. The former is allocated to G. mrginuta Bergh, 1868 and the latter to G. atlanticuc Forster, 1777. Glaucilla has multiseriate ceratal clusters (uniseriate in Glaucus) , an unarmed penis (armed with a chitinous spine in Glaucas ) and several anatomical peculiarities. Glaucid nudibranchs feed upon species of Velella, Physalia and Porpita ; nematocysts of Physalia are subsequently employed for defence. Both Glaucus and Glaucilla are potentially harmful to man.     

Aeolid nudibranchs (Gastropoda: Opisthobranchia) of the family Glaucidae from New Zealand waters

Two new species of aeolid, a new genus being created for one of them, are described along with another two species, one Phidiana militaris (Alder & Hancock) (= Learchis militaris ) a new record for New Zealand, the other, Glaucus atlanticus , found only once before. Jason mirabilis gen. et sp. nov. is distinguished by a ventral tongue-like process with a ridged chitinous covering which replaces the radula (still present but vestigial) and by the greatly subdivided rhinophoral lamellae. Babaina caprinsulensis sp. nov. differs from its Californian relative in having papillate rhinophores. The New Zealand specimens of Phidiana militaris differ slightly in colouration from those described for elsewhere in the Indo-Pacific.
The Glaucidae is enlarged to include the Babainidae, Facelinidae and Favorinidae, the main familial characteristics being the simple oral glands, sharp radular tooth and pugnacious behaviour. Possible evolutionary trends within the family based on the arrangement of the cerata and penial structure are traced out. The Babaininae, pleuroproctic with a notal ridge and irregular disposition of the cerata, is considered the most primitive subfamily and the Hervellinae, with cerata in single rows, the most advanced. The many facelinid genera previously recognized are reduced to two, Antionetta Schmekel and Phidiana Gray.     

The anatomy and biology of alcyonarian-feeding aeolid opisthobranch molluscs and their development of symbiosis with zooxanthellae

The anatomy of seven species of aeolid opisthobranch molluscs is described. They are all considered to be specialized feeders on alcyonarian coelenterates and to belong to one genus Phyllodesmium (Glaucidae; Favorininae). Two species are considered to be new. Favorinus horridus Macnae, Aeolidia poindimiei Risbec, Cratena macphersonae Burn and another species not studied in this paper, Hervia serrata Baba, are transferred to Phyllodesmium from the genera in which they are currently placed. Myrrhine Bergh, Babaiella Risso-Dominguez and Phyllodesmiopsis Risso-Dominguez are considered synonyms of Phyllodesmium. The two new species feed on Xenia and P. poindimiei feeds on Telesto. It is shown that the species of Phyllodesmium exhibit an evolutionary series in the development of symbiosis with zooxanthellae. The zooxanthellae are obtained from the alcyonarians upon which the aeolids feed. Morphological peculiarities present in some members of the genus are considered to be associated with the symbiosis.     

Insights gained from a web-based atlas of halocyprid ostracods of the Southern Ocean

Planktonic ostracods are an important, but poorly studied component of open ocean plankton communities, which inhabit all depths and play a significant role in detrital cycles. A web-based atlas (http://ocean.iopan.gda.pl/ostracoda) of the distribution of Southern Ocean planktonic ostracods has been developed compiling all extractable published data together with a considerable amount of unpublished data from samples collected during Discovery investigations (1929–1952). The northern boundary of the Southern Ocean was taken pragmatically as 52°S. The website includes information that includes distributional maps, taxonomic drawings (mostly original), size data and systematic notes on 47 species. All the data are freely downloadable as PDF files and are thus available to anyone, anywhere, with access to the web.Published data are subject to a number of errors generated by faulty identifications and changes in the taxonomy. Most, but not all, published data could be included in drawing up the maps. Not all publications have included detailed positional data and from those that included distributional maps, it was not always possible to relate the plotted distributions to the published station listings. A lack of archived data and specimens for some of the records meant dubious records could not be validated. Data are now generally archived by national oceanographic data centres, but unless supported by voucher specimens further confusion may arise for those current species which are found to include cryptic species after classical morphological studies or molecular studies.One species (Boroecia antipoda) had an apparently anomalous distribution; specimens archived in the Copenhagen Museum were reexamined and the anomalies were shown to result from the fact that some of the specimens belong to a novel species. Generally, the limits to the distributional ranges of the species showed little coherence with major oceanographic features, such as the Antarctic convergence and hence, biogeographical provinces; possible reasons are discussed. Despite these possible inherent errors, the website not only provides a resource for species identification, but is also proving to be a powerful tool for generation of hypotheses and highlighting taxonomic problems.     

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.     

Issue Information

Aeolidia papillosa (Linnaeus, 1761 ) is a well‐known aeolidiid species that has been reported to have a worldwide distribution in cold–temperate waters, mainly from the northern hemisphere. Molecular tools have recently shown that most cosmopolitan species usually belong to a taxonomic species complex. Here we used integrative taxonomy to test the range of distribution of A. papillosa, and to assess the existence of a putative species complex that has been traditionally included as a single species under the name A. papillosa. Maximum‐likelihood and Bayesian analyses of partial DNA sequences of the mitochondrial cytochrome c oxidase subunit I and 16S rRNA genes, and the nuclear gene histone 3, were used to infer phylogenetic trees. Automatic Barcode Gap Discovery (ABGD) species delimitation analyses and morphological study complemented the phylogenetic approach. Our results show that A. papillosa is a cosmopolitan and an amphi‐Atlantic species, being distributed in the eastern and western Atlantic as well as in the eastern Pacific; however, some specimens from the UK and the Netherlands, together with specimens from Portugal, Galicia, and France, as well as the Californian and Oregon populations, emerge as two pseudocryptic species described herein: Aeolidia filomenae  sp. nov. and Aeolidia loui  sp. nov. , respectively. Finally, the specimens from Chilean coasts, previously attributed to A. papillosa, belong to a different species, Aeolidia campbellii (Cunningham, 1871 ), that is a senior synonym of Aeolidia serotina Bergh, 1873 .     

On some species of Chelidonura (Opisthobranchia:Aglajidae) from Zanzibar and Fiji

The anatomy of specimens of Chelidonura philinopsis Eliot, 1903 and a new species of Chelidonura collected in Zanzibar, are described. Preserved specimens of Chelidonura, from Fiji, most probably C. varians Eliot, 1903 (=C. velutina Bergh, 1905) are discussed. Chelidonura philinopsis is compared with C. hirundinina {Quoy & Gaimard, 183 2) and it is suggested that at this stage they should remain as distinct species. C. punctata Eliot, 1903, the other species of the genus recorded from Zanzibar, is compared with two similarly coloured species from Japan, C. fulvipunctata, Baba, 1938 and C. tsurugensis, Baba & Abe, 1959.
The species suggest that the structure of the alimentary canal and the reproductive system (excluding the penis) are constant within the genus.     

Further studies on the anatomy and ecology of opisthobranch molluscs feeding on the scleractinian coral Pontes

Three further species of opisthobranch molluscs are reported to feed on the scleractinian coral Pontes in Tanzania. Further information on Cuthona poritophages Rudman, 1979, is also included. The anatomy of the aeolid Phestilla lugubris {Bergh, 1870, = P. sibogae Bergh, 1905) and a new species of Phestilla is described, as is the anatomy of the arminacean Pinufius rebus. The new species of Phestilla , and Pinufius , are, for the first time, reported to feed on Porites. Notes on the anatomy of the type-species of Phestilla, P. melanobrachia Bergh, 1874, are included to make possible a definition of the genus Phestilla.
Aspects of the feeding biology, life history, defence mechanisms and habitat specificity of the four Porites-feeding opisthobranchs are described and discussed. The four species are shown to have evolved radular teeth of remarkably similar shape. Each species utilizes a different part of the coral tissue as food. The three aeolids have replaced functional cnidosacs at the tip of their cerata with batteries of large secretory cells.
Phestilla lugubris and Pinufius rebus are also reported for the first time from the Great Barrier Reef, Queensland and the new species of Phestilla is reported from Queensland and Hawaii.     

Born‐digital biodiversity data: Millions and billions

Given the dramatic pace of change of our planet, we need rapid collection of environmental data to document how species are coping and to evaluate the impact of our conservation interventions. To address this need, new classes of “born digital” biodiversity records are now being collected and curated many orders of magnitude faster than traditional data. In addition to the millions of citizen science observations of species that have been accumulating over the last decade, the last few years have seen a surge of sensor data, with eMammal's camera trap archive passing 1 million photo‐vouchered specimens and Movebank's animal tracking database recently passing 1.5 billion animal locations. Data from digital sensors have other advantages over visual citizen science observation in that the level of survey effort is intrinsically documented and they can preserve digital vouchers that can be used to verify species identity. These novel digital specimens are leading spatial ecology into the era of Big Data and will require a big tent of collaborating organizations to make these databases sustainable and durable. We urge institutions to recognize the future of born‐digital records and invest in proper curation and standards so we can make the most of these records to inform management, inspire conservation action and tell natural history stories about life on the planet.     

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.     

Nesippus orientalis Heller, 1868 (Pandaridae: Siphonostomatoida): descriptions of the adult, young and immature females, a first description of the male and aspects of their functional morphology

Nesippus orientalis Heller, 1868, a cosmopolitan species found in the mouth and on the gill-arches of a number of shark hosts, is distinguished from other species by the presence of dorsal plates on the fourth thoracic segment. Specimens were collected from various sharks caught in the nets of the Natal Sharks Board, off the coast of KwaZulu-Natal, South Africa. Collected specimens were preserved in 70% ethanol and studied using the wooden slide technique and scanning electron microscopy. Careful examination of adult females revealed features previously not described in detail. Furthermore, some female specimens were still grasping the placoid scales of their hosts. These specimens showed how the maxillipeds are used to clasp the host. Immature, young females and males, some still attached to the young females, were also collected. The males use their maxillipeds, which have a slightly different structure to those of the female, to hold onto the females.     

Tripterygion atlanticus sp. nov. (Teleostei–Tripterygiidae) the first record of a tripterygiid fish in North-Western Europe

A northward extension of the range of the family Tripterygiidae is reported. Several specimens have been captured in the vicinity of Roscoff, North Finisterrc on the coast of Britanny, and presumed sight records from the English coast of the English Channel are reported. These specimens differ sufficiently from the four recognized European species to be regarded as taxonomically distinct. The name Tripterygion atlanticus is proposed for this species which is formally described.     

A Preliminary Account of the Tardigrades of Newfoundland

This is the first published report of tardigrades in Newfoundland and Labrador. Twenty-six species have been identified so far, including four new records for Canada and one new record for North America. Although there is some overlap of species with those found in earlier Canadian studies, there are some interesting discrepancies. The rare occurrence and restricted distribution of the very few heterotardigrades (three species and 30 specimens) found so far in Newfoundland is noteworthy, as is the occurrence of several tardigrade species whose former records have been mainly for Greenland. It appears the environmental conditions in Newfoundland can support a number of species that would normally be restricted to a more northerly distribution. A comparison of the species found in Newfoundland with those of a number of other northern countries suggests that the Newfoundland species are most similar to those found in Greenland and mainland Canada.     

角姬蜂属一新种(膜翅目：姬蜂科)

角姬蜂属CosmoconusFoerster,1868隶属柄卵姬蜂亚科Tryphoninae[1]、柄卵姬蜂族Tryphonini。迄今为止,全世界已知23种,其中东洋区1种,古北区13种,新北区9种。我国已知3种[2,3]：中国角姬蜂C．chinensisKasparyan,1973分布于西藏;中角姬蜂C．meridionatorAubert,1963分布于内蒙古及欧洲;西藏角姬蜂C．tibeticusKasparyan,1971分布于西藏和甘肃。属征：前翅第2脉在中央上方强度锯齿形曲折;额中央有一个角状突或乳状突。本文报道来自沈阳的本属一新种。模式标本保存在林业部森林病虫害防治总站。沈阳角姬问Cosm。sshenyangensi…     

宽额甲属分类研究(鞘翅目,拟步甲科)

对宽额甲属Ascelosodis昆虫进行了分类研究.描述采自中国西藏3新种,即小粒宽额甲A.granata sp.nov.,郑氏宽额甲A.zhengi sp.nov.和班戈宽额甲A.baingoinana sp.nov..给出了已知种名录和检索表.模式标本保存于河北大学博物馆.