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Thirty-six species of various thecate hydroids occur in two recent, deep-water collections from off New Caledonia. Of these, nine are new, namely Solenoscyphus subtilis Galea, sp. nov., Hincksella immersa Galea, sp. nov., Synthecium rectangulatum Galea, sp. nov., Diphasia alternata Galea, sp. nov., Dynamena opposita Galea, sp. nov., Hydrallmania clavaformis Galea, sp. nov., Symplectoscyphus acutustriatus Galea, sp. nov., Symplectoscyphus elongatulus Galea, sp. nov. and Zygophylax niger Galea, sp. nov. The male and female gonothecae of Caledoniana decussata Galea, 2015, the female gonothecae of Caledoniana microgona Galea, 2015, as well as the gonothecae of both sexes of Solenoscyphus striatus Galea, 2015 are described for the first time. The systematic position of the genera Solenoscyphus Galea, 2015 and Caledoniana Galea, 2015 is discussed on both morphological and molecular grounds, and both are confidently placed within the family Staurothecidae Maronna et al., 2016. In light of the molecular data, the genera Billardia Totton, 1930 and Dictyocladium Allman, 1888 are assigned to the families Syntheciidae Marktanner-Turneretscher, 1890 and Symplectoscyphidae Maronna et al., 2016, respectively. The previously undescribed gonothecae of Hincksella neocaledonica Galea, 2015, and the male gonothecae of Sertularella tronconica Galea, 2016, were found. Thyroscyphus scorpioides Vervoort, 1993, a peculiar hydroid with putative stem nematothecae, is redescribed and assigned to the new genus Tuberocaulus Galea, gen. nov. Noteworthy new records from the study area are: Tasmanaria edentula (Bale, 1924), Hincksella sibogae Billard, 1918, Dictyocladium reticulatum (Kirchenpauer, 1884), Salacia sinuosa (Bale, 1888) and Billardia hyalina Vervoort & Watson, 2003. Most species are illustrated to facilitate their identification, and the morphology of the new ones is compared to that of their related congeners.
The Swedish species of Ophion Fabricius, 1798 are revised. More than 4800 specimens and relevant type material were studied; 234 sampled specimens produced COI sequences. The study recognises 41 species, 18 of which are described as new to science, mainly from Fennoscandian material: Ophion angularis Johansson & Cederberg sp. nov., Ophion arenarius Johansson sp. nov., Ophion autumnalis Johansson sp. nov., Ophion borealis Johansson sp. nov., Ophion broadi Johansson sp. nov., Ophion brocki Johansson sp. nov., Ophion confusus Johansson sp. nov., Ophion ellenae Johansson sp. nov., Ophion inclinans Johansson sp. nov., Ophion kallanderi Johansson sp. nov., Ophion matti Johansson sp. nov., Ophion norei Johansson sp. nov., Ophion paraparvulus Johansson sp. nov., Ophion paukkuneni Johansson sp. nov., Ophion splendens Johansson sp. nov., Ophion sylvestris Johansson sp. nov., Ophion tenuicornis Johansson sp. nov. and Ophion vardali Johansson sp. nov. Barcoding analysis also indicated the possible presence of at least three additional, partly cryptic species, but these cannot be separated morphologically with certainty at this point. Ophion costatus Ratzeburg, 1848 and Ophion artemisiae Boie, 1855 are interpreted and defined. Ophion slaviceki Kriechbaumer, 1892 is excluded from synonymy with Ophion luteus Linnaeus, 1758 stat. rev. Ophion polyguttator (Thunberg, 1824) stat. rev. and Ophion variegatus Rudow, 1883 stat. rev. are excluded from synonymy with O. obscuratus Fabricius, 1798. Ophion variegatus is redescribed and a neotype is designated. Ophion albistylus Szépligeti, 1905 (syn. nov.) is synonymized with Ophion pteridis Kriechbaumer, 1879 and Ophion frontalis Strobl, 1904 (syn. nov.) is synonymized with Ophion areolaris Brauns, 1889 syn. nov. Eleven species are reported from Sweden for the first time: Ophion artemisiae, Ophion crassicornis Brock, 1982, Ophion costatus, Ophion dispar Brauns, 1895, Ophion forticornis Morley, 1915, Ophion kevoensis Jussila, 1965, Ophion ocellaris Ulbricht, 1926, Ophion perkinsi Brock, 1982, Ophion subarcticus Hellén, 1926, Ophion variegatus Rudow, 1883 and Ophion wuestneii Kriechbaumer, 1892. The study shows that a number of species that previously have been treated as highly variable taxa, actually consist of several valid species that are separable using morphological characters. An illustrated key for the determination of the Swedish Ophion species is provided.
We present an updated, subjective list of the extant, non-marine ostracod genera and species of the world, with their distributions in the major zoogeographical regions, as well as a list of the genera in their present hierarchical taxonomic positions. The list includes all taxa described and taxonomic alterations made up to 1 July 2018. Taxonomic changes include 17 new combinations, 5 new names, 1 emended specific name and 11 new synonymies (1 tribe, 4 genera, 6 species). Taking into account the recognized synonymies, there are presently 2330 subjective species of non-marine ostracods in 270 genera. The most diverse family in non-marine habitats is the Cyprididae, comprising 43.2% of all species, followed by the Candonidae (29.0%), Entocytheridae (9.1%) and the Limnocytheridae (7.0%). An additional 13 families comprise the remaining 11.8% of described species. The Palaearctic zoogeographical region has the greatest number of described species (799), followed by the Afrotropical region with 453 species and the Nearctic region with 439 species. The Australasian and Neotropical regions each have 328 and 333 recorded species, respectively, while the Oriental region has 271. The vast majority of non-marine ostracods (89.8%) are endemic to one zoogeographical region, while only six species are found in six or more regions. We also present an additional list with 'uncertain species', which have neither been redescribed nor re-assessed since 1912, and which are excluded from the main list; a list of taxonomic changes presented in the present paper; a table with the number of species and % per family; and a table with numbers of new species described in the 20-year period between 1998 and 2017 per zoogeographical region. Two figures visualize the total number of species and endemic species per zoogeographical region, and the numbers of new species descriptions per decade for all families and the three largest families since 1770, respectively.
Macrostemum is the second largest genus of Macronematinae with about 104 described species distributed in the Neotropical (18), Afrotropical (20), Australasian (7), Palearctic (2), Nearctic (3) and Oriental (54) regions. Despite its great diversity, knowledge about its immature stages is scarce: worldwide, only 7 species (6.7%) have larvae and/or pupae described. From the Neotropics, only one species, Macrostemum ulmeri (Banks, 1913), has described larvae and pupae. The objectives of this study are to describe and illustrate a new species, Macrostemum araca sp. nov., based on adult males and females from Serra do Aracá, Amazonas, Brazil, and the larvae and pupae of M. brasiliense (Fischer, 1970) from an Atlantic Forest fragment in São Paulo state using the metamorphotype method. In addition, this species is recorded for the first time for Minas Gerais state.
This paper describes a set of guidelines for the citation of zoological and botanical specimens in the European Journal of Taxonomy. The guidelines stipulate controlled vocabularies and precise formats for presenting the specimens examined within a taxonomic publication, which allow for the rich data associated with the primary research material to be harvested, distributed and interlinked online via international biodiversity data aggregators. Herein we explain how the EJT editorial standard was defined and how this initiative fits into the journal's project to semantically enhance its publications using the Plazi TaxPub DTD extension. By establishing a standardised format for the citation of taxonomic specimens, the journal intends to widen the distribution of and improve accessibility to the data it publishes. Authors who conform to these guidelines will benefit from higher visibility and new ways of visualising their work. In a wider context, we hope that other taxonomy journals will adopt this approach to their publications, adapting their working methods to enable domain-specific text mining to take place. If specimen data can be efficiently cited, harvested and linked to wider resources, we propose that there is also the potential to develop alternative metrics for assessing impact and productivity within the natural sciences.
The New Caledonia archipelago is known for its high level of endemism in both faunal and floral groups. Thus far, only 12 species of non-marine ostracods have been reported. After three expeditions to the main island of the archipelago (Grande Terre), about four times as many species were found, about half of which are probably new. Here, we describe a new species, Cyprinotus drubea sp. nov., which is characterised mainly by the hyper-developed dorsal hump on the right valve, much larger than in any other known Recent species in this genus. After a literature study of the other presumed species in Cyprinotus Brady, 1886, we retain seven Recent species in the genus, including the present new species. Cyprinotus crenatus (Turner, 1893), C. dentatus (Sharpe, 1910), C. flavescens Brady, 1898, C. inconstans Furtos, 1936, C. newmexicoensis Ferguson, 1967, C. ohanopecoshensis Ferguson, 1966, C. pellucidus (Sharpe, 1897), C. scytodus (Dobbin, 1941) and C. sulphurous Blake, 1931 are here all referred to the genus Heterocypris s. lat. Claus, 1892. Cyprinotus unispinifera Furtos, 1936 is assigned to the genus Cypricercus Sars, 1895. Cyprinotus tenuis Henry, 1923, C. fuscus Henry, 1919 and C. carinatus (King, 1855) are here classified as doubtful species. A checklist of the 14 non-marine ostracods, now including Cyprinotus drubea sp. nov. and Cypris granulata (Daday, 1910), thus far reported from New Caledonia, is provided. Herpetocypris caledonica Méhes, 1939 and H. caledonica var. minor Méhes, 1939 are synonymised with Candonocypris novaezelandiae (Baird, 1843).
We provide the first comprehensive taxonomic revision of the poorly known South American butterfly genus Zischkaia Forster, 1964, hitherto regarded as including three described species. A phylogenetic analysis based on DNA sequence data shows that Zischkaia is monophyletic and consists of two morphologically diagnosable clades. Morphological characters and DNA 'barcodes' support the recognition of twelve species in the genus, a significant increase even for the relatively poorly studied subtribe Euptychiina. Consequently, nine new species are described and named herein, including Z. arctoa Nakahara, sp. nov., Z. chullachaki Nakahara & Zacca, sp. nov., Z. baku Zacca, Dolibaina & Dias, sp. nov., Z. arenisca Nakahara, Willmott & Hall, sp. nov., Z. argyrosflecha Nakahara, L. Miller & Huertas, sp. nov., Z. abanico Nakahara & Petit, sp. nov., Z. josti Nakahara & Kleckner, sp. nov., Z. mielkeorum Dolibaina, Dias & Zacca, sp. nov. and Z. warreni Dias, Zacca & Dolibaina, sp. nov. In addition, a neotype is designated for Satyrus pacarus Godart, [1824], and lectotypes are designated for Euptychia amalda Weymer, 1911, Euptychia fumata Butler, 1867 and Euptychia saundersii Butler, 1867.
The world species of Netomocera Bouček, 1954 (Hymenoptera Linnaeus, 1758: Pteromalidae Dalman, 1820), excluding those from the Oriental region, are revised. The Oriental species are excluded because their types could not be examined, the species limits could not be reliably assessed based on original descriptions and available Oriental material was scarce. Eighteen species, including 11 species described as new, are recognized: N. africana Hedqvist, 1971; N. alboscapus Hedqvist, 1971; N. amethysta sp. nov.; N. celebensis sp. nov.; N. cyanocephala sp. nov.; N. desaegeri sp. nov.; N. formiciformis sp. nov.; N. gloriosa sp. nov.; N. irregularis sp. nov.; N. masneri sp. nov.; N. merida sp. nov.; N. meridionalis sp. nov.; N. nearctica Yoshimoto, 1977; N. ramakrishnai Sureshan, 2010; N. rufa Hedqvist, 1971; N. sedlaceki Bouček, 1988; N. setifera Bouček, 1954; N. virgata sp. nov. The female brachypterous form of N. nearctica and the male of N. alboscapus are described for the first time. A key to both sexes is provided, as well as diagnoses, descriptions and illustrations for all treated species. The genus is reported for the first time in the Neotropical region. For several species, new distributional records are also given.
Telegeusinae is a small subfamily of Elateroid beetles presently attached to the Omethidae family. Pseudotelegeusis Wittmer, 1976 is composed of three species, two occurring in northern South America and one in Mexico. Here we describe the fourth species for the genus, Pseudotelegeusis meloi sp. nov., collected in a Malaise sample from the region of Madre de Dios, Peru. The new species is diagnosed mainly by the antennae serrate from antennomeres III to X, eyes occupying half of head width in lateral view and vertex occupying 3/5 of head in dorsal view. This new species is close to the other two South American species, P. howdeni Wittmer, 1976 and P. oculatus Wittmer, 1976, according to the serrate antennae and number of ventrites. The three South American species differ from the Mexican species, P. jiliotupaensis Zaragoza-Caballero, 2008, by the different antennae and the number of ventrites, which indicates that the Mexican species should possibly be classified in a different genus. The main morphological characters, including maxillar palpi, tentorial pits and male genitalia, are illustrated, and an updated key to the species of Pseudotelegeusis is given, as well as distribution maps.
Twenty-two samples of Leptoclinides Bjerkan, 1905 collected along the Brazilian coast between 1998 and 2017 were examined. Herein we describe two new species (Leptoclinides coronatus sp. nov. and Leptoclinides lotufoi sp. nov.). We also extend the distribution of L. latus F. Monniot, 1983 and report that, for the first time, L. torosus F. Monniot, 1983 was found outside its type locality.
The genus Corambis Simon, 1901 includes five species; three of them, C. jacknicholsoni sp. nov., C. logunovi sp. nov. and C. pantherae sp. nov., are described here as new. The female of the C. foeldvarii Szűts, 2002 is described for the first time and a new generic diagnosis is proposed. The distribution and relationships of Corambis are discussed in terms of the geological and bioclimatic history of New Caledonia.
Two new nematode species of the genus Tobrilus Andrássy, 1959 from Lake Baikal are described and illustrated. The first species Tobrilus elginus sp. nov. was found in the littoral zone of Maloye More Bays. The second species Tobrilus juliae sp. nov. dwells on bodies of dead sponges Lubomirskia baicalensis (Pallas, 1776). Tobrilus elginus sp. nov. is most similar to T. amabilis Tsalolikhin, 1974 and T. bekmanae Tsalolikhin, 1975. In contrast to the first species it has a shorter body and spicules, longer gubernaculum and a shorter supplements row. Its body is shorter and thinner, tail and supplement row are shorter and the vulva is more posterior as compared to the second species. The body size of Tobrilus juliae sp. nov. is most similar to T. securus Gagarin & Naumova, 2011 and T. saprophagus Naumova & Gagarin, 2017. From the first of these species it differs by the thinner body, shorter tail, comparatively shorter outer labial setae and shorter spicules. It differs from the second species by a thinner body, shorter male tail and shorter labial setae.
Two new species of the genus Lepidocyrtus Bourlet, 1839 from southern China are described here: L. (Acrocyrtus) huizhouensis sp. nov. from Guangdong Province and L. (Setogaster) wanningensis sp. nov. from Hainan Province. Lepidocytus (Acrocyrtus) huizhouensis sp. nov. is the fourth species of the subgenus reported from China and L. (Setogaster) wanningensis sp. nov. is the first report of the subgenus from China.
The majority of Ceraphronoidea (Insecta: Hymenoptera) species were described in the late 1800s and early 1900s, with most of these early descriptions relying on text alone. Few type specimens have been illustrated and even fewer have been photographed, posing a challenge to taxonomists working on the group today. Here, we attempt to remove the barriers obstructing Ceraphronoidea research by creating a photographic catalog of the type specimens present at the Muséum national d'Histoire naturelle (MNHN) in Paris, France. We discuss the history of the ceraphronoid specimens present in the collection and provide comments on unpublished species notes from former Ceraphronoidea taxonomist Paul Dessart. We synonymize Ceraphron myrmecophilus Kieffer, 1913 syn. nov. with Aphanogmus abdominalis (Thomson, 1858) (Hymenoptera: Ceraphronidae) based on the male genitalia morphology, body shape and presence of foveae on the median length of the mesoscutellum. We also report the discovery of the missing male holotype of Ceraphron testaceus (Risbec, 1953) (Hymenoptera: Ceraphronidae) and several potential types of Aphangomus aphidi (Risbec, 1955) (Hymenoptera: Ceraphronidae).
The taxa of Cryptocephalinae (Clytrini), Synetinae and part of Galerucinae introduced by Carl Peter Thunberg are reviewed based on the examination of primary type specimens deposited in the Museum of Evolution, Uppsala University. The following taxonomic changes are proposed: Coptocephala unifasciata unifasciata (Scopoli, 1763) = Cryptocephalus melanocephalus Thunberg, 1787 syn. nov.; Melitonoma decemnotata (Thunberg, 1787) comb. nov. (from Cryptocephalus Geoffroy, 1762); Miopristis flexuosa (Thunberg, 1821) = Miopristis namaquensis Medvedev, 1993 syn. nov.; Protoclytra ( Lacordairella) taeniata (Thunberg, 1821) comb. nov. (from Camptolenes Chevrolat, 1836) = Camptolenes fastuosa (Lacordaire, 1848) syn. nov.; Smeia undata (Thunberg, 1821) comb. nov. (from Miopristis Lacordaire, 1848) = Smeia virginea (Lacordaire, 1848) syn. nov. = Melitonoma pictipennis Jacoby, 1898 syn. nov.; Teinocera catenata (Thunberg, 1821) comb. nov. (from Miopristis) = Teinocera subclathrata (Lacordaire, 1848) syn. nov.; Exosoma lusitanica (Linnaeus, 1767) = Crioceris haemorrhoa Thunberg, 1827 syn. nov.; Megalognatha festiva (Fabricius, 1781) = Crioceris virens Thunberg, 1827 syn. nov.; Monolepta bioculata (Fabricius, 1781) = Cryptocephalus bioculatus Thunberg, 1827 syn. nov.; Monolepta melanogaster (Wiedemann, 1823) = Cryptocephalus capensis Thunberg, 1827 syn. nov.; Palaeophylia tricolor (Fabricius, 1781) = Crioceris tetrapuncta Thunberg, 1787 syn. nov. = Crioceris dimidiata Thunberg, 1827 syn. nov. Lectotypes are designated for Cryptocephalus bioculatus Thunberg, 1827 and Crioceris dimidiata Thunberg, 1827. Melitonoma decemnotata comb. nov. is redescribed. Labidostomis insidiosa Péringuey, 1888 is resurrected from synonymy with Teinocera catenata comb. nov. and provisionally placed as a valid species in the genus Miopristis Lacordaire, 1848. Crioceris betulina Thunberg, 1787 is proposed as nomen oblitum for Syneta betulae (Fabricius, 1792) (nomen protectum). Colour photographs of the type specimens of all taxa are provided.
Five new species of the genus Drosophila Fallén, 1823 belonging to the tripunctata group are described and illustrated: D. warmi sp. nov., D. kurillakta sp. nov., D. chichu sp. nov., D. saraguru sp. nov. and D. ayauma sp. nov. from the forests of Podocarpus National Park. The first species is ascribed to subgroup II of Frota-Pessoa (1954), the second species to subgroup IV, and the last three species are not assigned to any subgroup. The flies were captured using plastic bottles containing pieces of yeast fermented banana.
The African shieldbug genus Afrius Stål, 1870 is revised. Cantheconidea migratoria Distant, 1913 and A. williamsi Miller, 1952 are proposed as junior synonyms of A. (Subafrius) flavirostrum (Signoret, 1861) whereas Canthecona marmorata Dallas, 1851, Canthecona annulipes Dallas, 1851 and A. rubromarginatus Bergroth, 1903 are proposed as junior synonyms of A. (Afrius) purpureus (Westwood, 1837) based on the general morphology and genitalia of the species. The three valid species, viz. A. (Subafrius) flavirostrum, A. (Afrius) kolleri Schouteden, 1911 and A. (Afrius) purpureus, are redescribed with details of male and female genitalia morphology, and a lectotype is designated for A. (Afrius) kolleri. A key to identify the species as well as an update of the geographical distribution for each species are provided, including new records for A. (Afrius) purpureus.
The new genus and species Campydoroides manautei Holovachov gen. et sp. nov. is placed in the suborder Campydorina and is characterised by a transversely striated cuticle without lateral alae, body pores or epidermal glands; somatic sensilla only on pharyngeal region and on tail; a truncate labial region with papilliform inner labial, outer labial and cephalic sensilla; a stirrup-shaped amphid with transverse slit-like opening; a conoid stoma with strongly cuticularised walls and large protrusible dorsal tooth; a cylindrical pharynx with distinct basal bulb but without valves; a large ovoid cardia; didelphic, amphidelphic female gonads with antidromously reflexed ovaries and without spermatheca; a transverse vulva; a straight vagina without pars refringens vaginae or epiptygmata; an elongate tail with caudal glands and spinneret. The new genus is similar to the genera Campydora Cobb, 1920 and Udonchus Cobb, 1913 in having papilliform labial and cephalic sensilla, a stirrup-shaped amphid with a transverse slit-like opening, a stoma with a well-developed protrusible dorsal tooth, and a muscular pharynx with a strongly developed basal bulb, but can be easily separated from both in details of a stoma morphology. The systematics of the suborder Campydorina is revised. Halirhabdolaimus Siddiqi, 2012 is synonymised with Syringolaimus de Man, 1888.
Polysyncraton Nott, 1892 is the second largest genus of didemnid ascidians; it has a wide distribution ranging from temperate to tropical waters. Seventy-one specimens of Polysyncraton from eight museum collections and recently collected samples were analyzed. This resulted in the description of three new species (P. cabofriense Oliveira & Rocha sp. nov. from Brazil, P. globosum Oliveira & Rocha sp. nov. from Australia and P. snelliusi Oliveira & Rocha sp. nov. from Suriname) and emended descriptions of three further species (P. amethysteum (Van Name, 1902), P. magnilarvum (Millar, 1962) and P. purou C. Monniot & F. Monniot, 1987).
Several taxonomic groups within Empidoidea Latreille, 1809 have been subject to unclear phylogenetic assignments along with multiple parallel hypotheses causing difficulties in classification and morphological identification. This study reviews the internal classification of the Ragadidae and includes a diagnosis and description of all included subfamilies and genera based on the results of an analysis of morphological characters using maximum parsimony. Illustration of important characters and a key to all genera in the family is given. The genus Hormopeza Zetterstedt, 1838 is found to be most closely related to Anthepiscopus Becker, 1891 and Iteaphila Zetterstedt, 1838, and the subfamily Iteaphilinae Wahlberg & Johanson, 2018 is therefore expanded to also include that genus. Hormopeza is consequently excluded from Ragadinae Sinclair, 2016. This study provides diagnoses, descriptions and keys in a contribution to a thorough classification of the empidoid groups and increased ease in morphological recognition.