European journal of taxonomy : EJT
Paris : Muséum National d'Histoire Naturelle
ISSN: 2118-9773
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Review of Neurepyris Kieffer, 1905 (Hymenoptera, Bethylidae), a new synonym of Pristocera Klug, 1808
(2011)
The genus Neurepyris Kieffer, 1905 is revised. The adult male holotypes N. rufiventer Kieffer, 1913 from Eritrea and N. tagala (Ashmead, 1905) from the Philippines are redescribed and illustrated. Both species are transferred from the subfamily Epyrinae to Pristocerinae because they have the metanotum well developed medially. Neurepyris rufi venter is transferred to Pristocera Klug, 1808 because the hypopygium is deeply divided into two apical lobes, the subdiscoidal and cubital veins do not reach the border of the forewing, the pronotal disc has the anterior region slightly elevate medially, and the stigma is elongate. Neurepyris tagala is transferred to Apenesia Westwood, 1874 because the basal tooth of mandible is not curved inward, the median lobe of clypeus is not depressed near the antennal insertions, and the aedeagus consists of one lamina. The genus Neurepyris is considered a junior synonym of Pristocera because its type species is N. rufiventer.
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We are very pleased and proud to announce the launch of the European Journal of Taxonomy. The EJT is an international, online, fast-track, peer-reviewed, open access journal in descriptive taxonomy,covering subjects in zoology, entomology, botany, and palaeontology, owned and run by a Consortium of European Natural History Institutes. EJT is a collaborative project outcome of the EDIT network.
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A new gymnophthalmid lizard of the genus Anadia Gray, 1845 is described from the summit of Abakapá-tepui, Bolívar State, Venezuela, between 2200-2242 m elevation. The new species, Anadia mcdiarmidi sp. nov., is endemic to the Chimantá Massif and seemingly also occurs on Amurí-tepui and Murei-tepui. The new taxon is mainly distinguished from all known congeners by the following combination of characters: body fairly robust, dorsal scales small and quadrangular, middorsal scales 53-57, suboculars large, subequal in size, with sometimes one scale slightly protruding downward between 4th and 5th supralabial, nasal entire, without sub-nostril groove, body uniform beige or greyish to bluish brown in life, devoid of any conspicuous pattern in males, venter immaculate golden grey in life, femoral pores 9-10 on each side in males, preanal pores absent, hemipenis globose, weakly bilobed, bordered by numerous fl ounces (>20) bearing comblike rows of minute weakly mineralized spinules. The presence of a species of Anadia, a primarily Andean genus, on the top of tepuis is of considerable interest to the understanding of the Pantepui biogeography.
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A new common deep-sea species of Halirages Boeck, 1871 closely related to H.qvadridentatus G.O. Sars, 1877, H.cainae sp. nov., is described after specimens collected in the Norwegian Sea during the MAREANO 2009-111 cruise. Examination of the syntypes of H. elegans Norman, 1882 demonstrates that Norman's species is a junior synonym of H.qvadridentatus G.O. Sars, 1877 and that the species usually named H.elegans in literature was actually undescribed. The name H.stappersi sp. nov. is proposed for that species. A key to and a checklist of Halirages species is given.
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New species Campsicnemus flavissimus sp. nov., C. meridionalis sp. nov., and C. sanctaehelenae sp. nov. are described from St. Helena. A review and key to seven Campsicnemus species inhabiting Azores, Canary Is., Madeira and St. Helena are provided. A new status (as subspecies of C. armatus Zetterstedt, 1849) for C. caffer Curran, 1926 stat. nov. is proposed.
18
Sponges belonging to the genera Amphilectus Vosmaer, Esperiopsis Carter and Ulosa de Laubenfels of the family Esperiopsidae were collected during 1986 and 1988 expeditions of the Netherlands Centre for Biodiversity Naturalis (at that time the National Museum of Natural History at Leiden and the Zoological Museum of Amsterdam) in waters off the coasts of Mauritania and the Cape Verde Islands. Four new species, Amphilectus utriculus sp. nov., Amphilectus strepsichelifer sp. nov., Esperiopsis cimensis sp. nov., Ulosa capblancensis sp. nov., and two already known species, Amphilectus cf. fucorum (Esper) and Ulosa stuposa (Esper) are described and discussed.
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An account of the taxonomic position of the genus Bracon Fabricius, 1804 is presented. In his monograph Wesmael (1838: 7-58) made a survey of 48 nominal species of Bracon occurring in Belgium. Out of the 48 species thirty-seven were described by Wesmael himself as new species, eleven more species had previously been described by Fabricius (three species), Nees (seven species) and Spinola (one species). The Bracon material studied by Wesmael is deposited in the Royal Belgian Institute of Natural Sciences, Brussels. Type (holo-, lecto-, paralectotype) designations are made for Wesmael’s species and neotype designations for Nees sensu Wesmael’s species. Redescriptions, comments on distributions and their taxonomic positions are presented. Palpibracon subgen. nov. is established (type species Bracon delibator Haliday, 1833) for fi ve Bracon species with long maxillary palpi in the Holarctic (four species) and Ethiopian Region (one species). The following fifteen Bracon species names proved to be junior synonyms (valid names in italics): B. dichromus Wesmael, 1838 = B. carpaticus Niezabitowski, 1910 syn. nov.; B. erraticus Wesmael, 1838 = B. bellicosus Papp, 1971 syn. nov., = B. exarator Marshall, 1885 syn. nov., = B. praetermissus Marshall, 1885 syn. nov., B. vectensis Marshall, 1885 syn. nov.; B. fuscicornis Wesmael, 1838 = B. levicarinatus Niezabitowski, 1910 syn. nov.; B. immutator Nees, 1834 = B. breviusculus Wesmael, 1838 syn. nov.; B. intercessor Nees, 1834 = B. laetus Wesmael, 1838 syn. nov.; B. larvicida Wesmael, 1838 = B. crassiusculus Szépligeti, 1901 syn. nov.; B. longicollis Wesmael, 1838 = B. subcylindricus Wesmael, 1838 syn. nov.; B. megapterus Wesmael, 1838 = B. biimpressus Telenga, 1936 syn. nov.; B. nigratus Wesmael, 1838 = B. orbicularis Niezabitowski, 1910 syn. nov.; B. osculator Nees, 1811 = B. coniferarum Fahringer, 1927 (Schmiedeknecht in litt.) syn. nov.; B. picticornis Wesmael, 1838 = B. vitripennis Ratzeburg, 1852 syn. nov.; B. titubatus Wesmael, 1838 = B. fuscipennis Wesmael, 1838 syn. nov. The species Bracon (Lucobracon) turolus Papp, 1984 is revalidated (suppressed under the name B. (Glabrobracon) nigriventris Wesmael, 1838 by Tobias & Belokobylskij 2000: 162). A historic discussion of the subgeneric division of the Bracon species is given.
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Australia is predicted to have a high number of currently undescribed ostracod taxa. The genus Bennelongia De Deckker & McKenzie, 1981 (Crustacea, Ostracoda) occurs in Australia and New Zealand, and has recently shown potential for high speciosity, after the description of nine new species from Western Australia. Here, we focus on Bennelongia from eastern Australia, with the objectives of exploring likely habitats for undiscovered species, genetically characterising published morphological species and scanning classical species for cryptic diversity. Two traditional (morphological) species are confi rmed to be valid using molecular evidence (B. harpago De Deckker & McKenzie, 1981 and B. pinpi De Deckker, 1981), while three new species are described using both morphological and molecular evidence. Two of the new species belong to the B. barangaroo lineage (B. dedeckkeri sp. nov. and B. mckenziei sp. nov.), while the third is a member of the B. nimala lineage (B. regina sp. nov.). Another species was found to be genetically distinct, but is not formally described here owing to a lack of distinguishing morphological features from the existing species B. cuensis Martens et al., 2012. Trends in diversity and radiation of the genus are discussed, as well as implications these results have for the conservation of temporary pool microfauna and our understanding of Bennelongia’s evolutionary origin.
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The present study describes five new free-living nematode species and provides three new species records of the family Comesomatidae (genera Cervonema Wieser, 1954, Dorylaimopsis Ditlevsen, 1918, Hopperia Vitiello, 1969, and Kenyanema Muthumbi et al., 1997) from the continental margin of New Zealand, Southwest Pacific. Dichotomous identification keys are provided for all known species of Dorylaimopsis and Hopperia. Cervonema shiae Chen & Vincx, 2000 is recorded for the first time outside the type locality (Beagle Channel, Chile). C. kaikouraensis sp. nov. is characterised by amphideal fovea with 5.5 turns situated at 1.7 head diameter from anterior end, jointed outer labial setae, equal in length to cephalic setae, sperm dimorphism, and 5-6 small pre-cloacal supplements. C. multispira sp. nov. is characterised by amphideal fovea with 8.0-8.5 turns situated at 2.6-4.0 head diameter from anterior end, cephalic setae 2-3 μm long, slightly shorter than outer labial setae, presence of six uninucleated cells in males (potentially pseudocoelomocytes or supplementary excretory cells), 5 small pre-cloacal supplements, and strongly cuticularised, arcuate spicules with capitulum. C. proberti sp. nov. is characterised by amphideal fovea with 5 turns and located at < 1 head diameter from anterior end, cephalic setae 1.6-2.0 times longer than outer labial setae, and 8 small pre-cloacal supplements. Dorylaimopsis nodderi sp. nov. is characterised by cuticle with lateral differentiation consisting of three longitudinal rows of larger dots in the pharyngeal and caudal regions, two rows of larger dots in middle region of body, and spicules with rounded ventral projection at one third of spicule length from distal end, giving appearance of a joint. Hopperia ancora sp. nov. is characterised by short conical cephalic setae, spicules with hook-like projection at distal end, gubernaculum with bent apophyses, and 11-13 pre-cloacal supplements. H. beaglense Chen & Vincx, 1998 is recorded from Kaikoura Canyon, the fi rst record of this species outside the type locality (Beagle Channel, Chile). Kenyanema monorchis Muthumbi et al., 1997 is also recorded for the first time outside the type locality (Indian Ocean).