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Drepanosticta kosterini sp. nov. (holotype ♂, from Gunung Penrissen, Kuching Division, Sarawak, Malaysian Borneo, deposited in RMNH) is described from both sexes. It is the sister species of D. actaeon Laidlaw, 1934; a fresh description of the male of D. actaeon and the first description of the female are given, along with discussion of variation in this species. Both D. actaeon and D. kosterini are considered to belong to a species group also including D. rufostigma (Selys, 1886) and a preliminary discussion of variation in this species is given, along with illustrations of both sexes. A neighbour joining COI gene tree for D. actaeon and D. kosterini is presented. The relationships of D. actaeon, D. kosterini and D. rufostigma to other members of the Platystictidae are briefly discussed.
The New World genus Chariessa Forster (Coleoptera: Cleroidea: Cleridae) is revised and includes C. catalina Opitz, new species, C. elegans Horn, C. dichroa (LeConte), C. floridana Schaeffer, C. pilosa (Forster), C. texana Wolcott, C. ramicornis Perty, C. vestita (Chevrolat), and C. duponti (Spinola). Enoplium pilosa var. marginata Say is synonymized with Chariessa pilosa Forster. Lectotypes are designated for C. pilosa (Forster), C. ramicornis Perty, and C. vestita (Chevrolat). Available information indicates that Chariessa adult and immature individuals are predatory on lignicolous insects with a particular affinity for cerambycids and buprestids that infest species of oak. It is postulated that Pleistocene speciation generated the North American components of Chariessa with more ancient southern species generated during the Middle Tertiary; after closures of the Middle American portals and orogeny of the South American Andes. Included in this treatise is a discussion of natural history, key to species, narratives of zoogeography and phylogeny, one diagram of a phylogenetic tree, 35 line drawings, eight SEM micrographs, twelve habitus photographs, nine photographs of male genitalia, and five distributional maps.
Three new scale insect species, Coccidohystrix daedalea Gavrilov-Zimin sp. nov., Mirococcopsis ptilura Gavrilov-Zimin sp. nov. (both from the family Pseudococcidae) and Cryptinglisia millari Gavrilov-Zimin sp. nov. (family Coccidae), are described and illustrated from the Western Cape Province of South Africa.
Five species of the terrestrial diatom genus Luticola D.G.Mann were found during a taxonomic survey of two small volcanic islands, Ile Amsterdam and Ile Saint-Paul (Southern Indian Ocean). Apart from the two already known Luticola species L. beyensii Van de Vijver et al. and L. subcrozetensis Van de Vijver et al., two new species are described: L. ivetana Chattová & Van de Vijver sp. nov. and L. vancampiana Chattová & Van de Vijver sp. nov. Finally, one, up to now unknown, Luticola species is briefly discussed and illustrated. Detailed morphological descriptions of these taxa are provided based on both light and scanning electron microscopy observations. Morphological features of the new species are compared to morphologically similar taxa, and notes on their ecology and biogeography are added.
We review the three species currently placed in the genus Xylopertha Guérin-Méneville, 1845, and describe a new species, Xylopertha elegans sp. nov., from Turkey. We propose the following new synonymy: Xylopertha Guérin-Méneville, 1845 (= Paraxylogenes Damoiseau, 1968); Xylopertha reflexicauda (Lesne, 1937) (= Paraxylogenes pistaciae Damoiseau, 1968). We give details of the sexual dimorphism, and summarise information on the distribution and biology of all species. A key to the species of Xylopertha is provided.
Siamopsis gen. nov., described here, belongs to a group of genera with the right valve overlapping the left valve in the subfamily Cypridopsinae Kaufmann, 1900 of the family Cyprididae Baird, 1845. The distinguishing characters of the new genus are in the morphology of its valves and soft parts. The postero-dorsal margin of the internal left valve is plate-like protruded. The morphology of this plate varies in different species, e.g., some species bear a tooth-like tubercle on the plate. The posterior margin of the right valve is recurved inwardly at ca mid-height, resulting in the occurrence of a lobe-like expansion that can clearly be seen in the dorsal and caudal views of the carapace. In addition, the other diagnostic soft part features of the new genus are the cylindrical caudal ramus, the presence of two t-setae on the female A2 penultimate segment, the very elongated terminal segment of the Mx1 palp, the morphology of the two large bristles (tooth bristles) of the Mx1 third endite (one smooth, one serrated) and the absence of d-seta on T1. In the present paper, five new species are described under this new genus: Siamopsis renateae gen. et sp. nov., S. suttajiti gen. et sp. nov., S. conspecta gen. et sp. nov., S. khoratensis gen. et sp. nov. and Siamopsis planitia gen. et sp. nov. A key to the species of Siamopsis gen. nov. is also provided.
Two species of the nematode family Diplopeltidae are described from Skagerrak. The new genus Belgopeltula gen. nov. is proposed for Diplopeltula belgica Vincx & Gourbault, 1992 and is characterised by: amphidial fovea circular in female and double-loop-shaped in male; excretory pore located at the level of cephalic setae bases; oral opening on the dorsal side of the body; pharynx subdivided into strongly muscularised fusiform corpus and weakly muscularised narrow and long postcorpus; female didelphic with antidromously reflexed ovaries; supplements absent. Mudwigglus micramphidium sp. nov. is characterised by: a body of 0.6 mm long; cephalic sensilla 1.5 μm long; amphidial fovea loop-shaped, 8 μm long and 3.5 μm wide; gymnostom without cuticularised ring; tail elongate conoid, with subcylindrical distal part; terminal setae absent; spicules 15 μm long; gubernaculum present; two midventral precloacal setae. It is distinguished from M. macramphidium Leduc, 2013 in having shorter amphidial fovea, shorter spicules and presence of two precloacal setae. Redescription of Diplopeltis cylindricauda Allgén, 1932 is provided based on type material. Diplopeltula minuta Vitiello, 1972 is transferred to the genus Mudwigglus Leduc, 2013. Diplopeltis cylindricauda Allgén, 1932, Diplopeltula laminata Vitiello, 1972 and Diplopeltula cassidaignensis Vitiello, 1972 are transferred to the genus Pseudaraeolaimus Chitwood, 1951.
Two Mastogloia Thwaites ex W.Sm. taxa were found during a survey of the diatom flora of Lac de Guiers, Senegal. Based on all currently available literature, one taxon could be identified as M. belaensis M.Voigt, a species formerly described from Pakistan. The second species showed some resemblance to M. braunii Grunow. Analysis of the type of M. braunii revealed, however, important morphologic differences, leading to the description of a new species from the Senegal population: M. senegalensis Van de Vijver, Fofana, Sow & Ector sp. nov. The present paper describes this new species and discusses and illustrates the morphology of M. belaensis and the type of M. braunii. All taxa are discussed with morphologically similar taxa.
Revision of the genus Spilopteron Townes, 1965 (Hymenoptera: Ichneumonidae: Acaenitinae) from Japan
(2017)
Ten Japanese species of the genus Spilopteron Townes, 1965 are recognized. Five new species, S. albiventre sp. nov., S. brachyurum sp. nov., S. nigrum sp. nov., S. oblongulum sp. nov. and S. pseudonigrum sp. nov., are described from Japan. Morphological discrimination between most Japanese species is confirmed by sequence analysis of the mitochondrial COI gene, which indicates the following relationships: S. oblongulum sp. nov. + S. apicale (Matsumura, 1912), S. brachyurum sp. nov. + S. nigrum sp. nov. + S. pseudonigrum sp. nov., and S. tosaense (Uchida, 1934) + S. luteum (Uchida, 1930). A key to the Japanese species of Spilopteron is provided. This genus seems to have its center of diversity in the mid-latitude area of East-Asia.
Species of Mortoniella are revised for the northern and Andean part of the South American continent, including the countries of Bolivia, Peru, Ecuador, Colombia, Venezuela, and Guyana. All previously described species from the region are reillustrated and redescribed, except for Mortoniella santiaga Sykora, 1999 and M. quinuas Harper and Turcotte, 1985, whose types could not be located, and M. tranquilla Martynov, 1912, whose type is based on a female specimen and thus is currently unidentifiable. Included in the revision are 35 described species and 59 new species. Mortoniella similis Sykora, 1999 is considered a junior synonym of M. roldani Flint, 1991, and M. macuta (Botosaneanu, 1998) is considered a junior synonym of M. limona (Flint, 1981). A new subgenus, Nanotrichia, is recognized to accommodate species previously referred to as members of the ormina and velasquezi groups. Mexitrichia pacuara Flint, 1974 is designated the type species for the subgenus. Species previously referred to as members of the bilineata and leroda species groups are retained in the nominate subgenus, along with additional taxa not previously placed to species group, and treated within a number of subgroups. Previously described species of M. (Mortoniella) which are redescribed and reillustrated include: M. angulata Flint, 1963; M. apiculata Flint, 1963; M. atenuata (Flint, 1963); M. bifurcata Sykora, 1999; M. bilineata Ulmer, 1906; M. bolivica (Schmid, 1958); M. chicana Sykora, 1999; M. denticulata Sykora, 1999; M. elongata (Flint, 1963); M. enchrysa Flint, 1991; M. flinti Sykora, 1999; M. foersteri (Schmid, 1964); M. hodgesi Flint, 1963; M. iridescens Flint, 1991; M. leei (Flint, 1974); M. limona (Flint, 1981); M. marini (Rueda Martín and Gibon, 2008); M. paralineata Sykora, 1999; M. paraenchrysa Sykora, 1999; M. pocita (Flint, 1983); M. punensis (Flint, 1983); M. roldani Flint, 1991; M. simla (Flint, 1974); M. spinulata (Flint, 1991); M. squamata Sykora, 1999; M. unilineata Sykora, 1999; and M. wygodzinskii (Schmid, 1958). New species described in M. (Mortoniella), followed by their respective areas of distribution, include: M. acutiterga (Ecuador); M. adamsae (Peru); M. akrogeneios (Ecuador); M. applanata (Peru); M. auricularis (Colombia); M. barinasi (Venezuela); M. biramosa (Venezuela); M. bothrops (Peru); M. brevis (Ecuador, Venezuela); M. bulbosa (Peru); M. catherinae (Peru); M. chalalan (Peru); M. cornuta (Peru); M. cressae (Venezuela); M. croca (Peru); M. curtispina (Venezuela); M. curvistylus (Ecuador); M. dentiterga (Ecuador); M. dinotes (Peru); M. draconis (Ecuador); M. emarginata (Ecuador, Colombia); M. esrossi (Colombia); M. flexuosa (Colombia); M. furcula (Ecuador); M. gilli (Ecuador); M. gracilis (Venezuela); M. grandiloba (Venezuela); M. guyanensis (Guyana); M. hamata (Colombia); M. langleyae (Ecuador); M. longiterga (Ecuador); M. membranacea (Bolivia); M. monopodis (Colombia, Ecuador); M. parameralda (Ecuador); M. pica (Ecuador); M. proakantha (Ecuador); M. prolata (Peru); M. quadrispina (Ecuador); M. rectiflexa (Ecuador); M. ruedae (Bolivia); M. schlingeri (Colombia); M. silacea (Colombia, Ecuador); M. sinuosa (Bolivia, Peru); M. spatulata (Venezuela); M. tanyrhabdos (Venezuela); M. tridens (Peru); M. triramosa (Bolivia); M. tusci (Venezuela); and M. variabilis (Venezuela, Colombia). Species assigned to the subgenus M. (Nanotrichia) which are redescribed and reillustrated include: M. aequalis (Flint, 1963); M. aries (Flint, 1963); M. collegarum (Rueda Martín and Gibon, 2008); M. eduardoi (Rueda Martín and Gibon, 2008); M. macarenica (Flint, 1974); M. pacuara (Flint, 1974); M. usseglioi (Rueda Martín and Gibon, 2008); and M. velasquezi (Flint, 1991). Previously described species of Mortoniella, outside the area of coverage, that are transferred to the subgenus M. (Nanotrichia) include: M. alicula Blahnik and Holzenthal, 2011; M. bocaina Blahnik and Holzenthal, 2011; M. catarinensis (Flint, 1974); M. froehlichi Blahnik and Holzenthal, 2011; M. ormina (Mosely, 1939); M. rodmani Blahnik and Holzenthal, 2008; and M. tripuiensis Blahnik and Holzenthal, 2011. New species in the subgenus M. (Nanotrichia), followed by their respective areas of distribution, include: Mortoniella cognata (Ecuador, Venezuela); M. coheni (Ecuador); M. licina (Ecuador); M. paucispina (Peru); M. quadridactyla (Venezuela); M. simplicis (Venezuela); M. spangleri (Ecuador); M. triangularis (Ecuador); M. venezuelensis (Venezuela); and M. zamora (Ecuador). A key to the males of species from the region is also provided, as well as a key to females for the major subgroups and a species key to females of the velasquezi group. Finally, a partially resolved phylogeny of the species is presented, along with a discussion of evolutionary trends within the genus.
The eight species in the genus Tomarus Erichson (Coleoptera: Scarabaeidae) in Argentina, Chile, and Uruguay are reviewed. Tomarus roigjunenti new species and Tomarus spinipenis new species are described from Argentina. We include a key to species, representative habitus illustrations for all species, character illustrations, and distribution maps for each, as well as commentary about the natural history and distributions for each species. Diagnostic characters are discussed for each species, and species relationships are hypothesized based on the analysis of internal and external morphological characters. The male of T. bidentulus (Fairmaire) is described for fi rst time. The following taxonomic changes are made: Tomarus guianucai Dechambre and Lumaret, 1985 is a new junior synonym of Tomarus rubripes (Boheman, 1858), which was formerly and incorrectly cited as occurring in Argentina.
The first myrmecophilous fl ea beetle genus (Myrmeconycha Konstantinov and Tishechkin, new genus) with four new species (M. erwini Konstantinov and Tishechkin, new species – Ecuador, M. gordoni Konstantinov and Tishechkin, new species – Brazil, M. pakaluki Konstantinov and Tishechkin, new species – Panama, and M. pheidole Konstantinov and Tishechkin, new species – Costa Rica) is described and illustrated. It is compared with fl ea beetles of the subtribe Disonychina (Coleoptera: Chrysomelidae: Galerucinae: Alticini) and may be easily differentiated based on the external and internal features, which include the waxy surface of the head and pronotum, reticulated surface of the pronotum, and four longitudinal ridges on each elytron.
Species of Mortoniella are revised for the northern and Andean part of the South American continent, including the countries of Bolivia, Peru, Ecuador, Colombia, Venezuela, and Guyana. All previously described species from the region are reillustrated and redescribed, except for Mortoniella santiaga Sykora, 1999 and M. quinuas Harper and Turcotte, 1985, whose types could not be located, and M. tranquilla Martynov, 1912, whose type is based on a female specimen and thus is currently unidentifiable. Included in the revision are 35 described species and 59 new species. Mortoniella similis Sykora, 1999 is considered a junior synonym of M. roldani Flint, 1991, and M. macuta (Botosaneanu, 1998) is considered a junior synonym of M. limona (Flint, 1981). A new subgenus, Nanotrichia, is recognized to accommodate species previously referred to as members of the ormina and velasquezi groups. Mexitrichia pacuara Flint, 1974 is designated the type species for the subgenus. Species previously referred to as members of the bilineata and leroda species groups are retained in the nominate subgenus, along with additional taxa not previously placed to species group, and treated within a number of subgroups. Previously described species of M. (Mortoniella) which are redescribed and reillustrated include: M. angulata Flint, 1963; M. apiculata Flint, 1963; M. atenuata (Flint, 1963); M. bifurcata Sykora, 1999; M. bilineata Ulmer, 1906; M. bolivica (Schmid, 1958); M. chicana Sykora, 1999; M. denticulata Sykora, 1999; M. elongata (Flint, 1963); M. enchrysa Flint, 1991; M. flinti Sykora, 1999; M. foersteri (Schmid, 1964); M. hodgesi Flint, 1963; M. iridescens Flint, 1991; M. leei (Flint, 1974); M. limona (Flint, 1981); M. marini (Rueda Martín and Gibon, 2008); M. paralineata Sykora, 1999; M. paraenchrysa Sykora, 1999; M. pocita (Flint, 1983); M. punensis (Flint, 1983); M. roldani Flint, 1991; M. simla (Flint, 1974); M. spinulata (Flint, 1991); M. squamata Sykora, 1999; M. unilineata Sykora, 1999; and M. wygodzinskii (Schmid, 1958). New species described in M. (Mortoniella), followed by their respective areas of distribution, include: M. acutiterga (Ecuador); M. adamsae (Peru); M. akrogeneios (Ecuador); M. applanata (Peru); M. auricularis (Colombia); M. barinasi (Venezuela); M. biramosa (Venezuela); M. bothrops (Peru); M. brevis (Ecuador, Venezuela); M. bulbosa (Peru); M. catherinae (Peru); M. chalalan (Peru); M. cornuta (Peru); M. cressae (Venezuela); M. croca (Peru); M. curtispina (Venezuela); M. curvistylus (Ecuador); M. dentiterga (Ecuador); M. dinotes (Peru); M. draconis (Ecuador); M. emarginata (Ecuador, Colombia); M. esrossi (Colombia); M. flexuosa (Colombia); M. furcula (Ecuador); M. gilli (Ecuador); M. gracilis (Venezuela); M. grandiloba (Venezuela); M. guyanensis (Guyana); M. hamata (Colombia); M. langleyae (Ecuador); M. longiterga (Ecuador); M. membranacea (Bolivia); M. monopodis (Colombia, Ecuador); M. parameralda (Ecuador); M. pica (Ecuador); M. proakantha (Ecuador); M. prolata (Peru); M. quadrispina (Ecuador); M. rectiflexa (Ecuador); M. ruedae (Bolivia); M. schlingeri (Colombia); M. silacea (Colombia, Ecuador); M. sinuosa (Bolivia, Peru); M. spatulata (Venezuela); M. tanyrhabdos (Venezuela); M. tridens (Peru); M. triramosa (Bolivia); M. tusci (Venezuela); and M. variabilis (Venezuela, Colombia). Species assigned to the subgenus M. (Nanotrichia) which are redescribed and reillustrated include: M. aequalis (Flint, 1963); M. aries (Flint, 1963); M. collegarum (Rueda Martín and Gibon, 2008); M. eduardoi (Rueda Martín and Gibon, 2008); M. macarenica (Flint, 1974); M. pacuara (Flint, 1974); M. usseglioi (Rueda Martín and Gibon, 2008); and M. velasquezi (Flint, 1991). Previously described species of Mortoniella, outside the area of coverage, that are transferred to the subgenus M. (Nanotrichia) include: M. alicula Blahnik and Holzenthal, 2011; M. bocaina Blahnik and Holzenthal, 2011; M. catarinensis (Flint, 1974); M. froehlichi Blahnik and Holzenthal, 2011; M. ormina (Mosely, 1939); M. rodmani Blahnik and Holzenthal, 2008; and M. tripuiensis Blahnik and Holzenthal, 2011. New species in the subgenus M. (Nanotrichia), followed by their respective areas of distribution, include: Mortoniella cognata (Ecuador, Venezuela); M. coheni (Ecuador); M. licina (Ecuador); M. paucispina (Peru); M. quadridactyla (Venezuela); M. simplicis (Venezuela); M. spangleri (Ecuador); M. triangularis (Ecuador); M. venezuelensis (Venezuela); and M. zamora (Ecuador). A key to the males of species from the region is also provided, as well as a key to females for the major subgroups and a species key to females of the velasquezi group. Finally, a partially resolved phylogeny of the species is presented, along with a discussion of evolutionary trends within the genus.
Recent expeditions (NANHAI 2014, DONGSHA 2014 and ZHONGSHA 2015) conducted in deep waters of the South China Sea obtained interesting material of various spider crabs (Majoidea) including several new records for the area, and two new species of epialtids of the genera Oxypleurodon Miers, 1885 and Stegopleurodon Richer de Forges & Ng, 2009. Two poorly known species, previously only known from their types, Rochinia strangeri Serène & Lohavanijaya, 1973 and R. kagoshimensis (Rathbun, 1932) comb. nov., are redescribed, refigured, and their taxonomy discussed.
A new genus and eight new species of urocyclid snails are described from eastern South Africa. The supra-specific taxa Kerkophorus Godwin-Austen, 1912 and Microkerkus Godwin-Austen, 1912 are considered distinct from Sheldonia Ancey, 1887 and are treated as separate genera. The diagnostic morphological features of all three genera are detailed and a fourth genus, for which there is no existing name, is described as new: Selatodryas gen. nov. A provisional key to genus-level taxa within Sheldonia s.l. is provided. Eight species are described as new: Kerkophorus piperatus sp. nov., K. vittarubra sp. nov., K. scrobicolus sp. nov., K. terrestris sp. nov., Microkerkus sibaya sp. nov., Selatodryas roseosoma gen. et sp. nov., S. luteosoma gen. et sp. nov. and Sheldonia fingolandensis sp. nov.
The genus Synaldis Foerster, 1863 is recorded in the Neotropical region for the first time. Five new Neotropical species, S. brasiliense Peris-Felipo, sp. nov., S. fritzi Peris-Felipo, sp. nov., S. longiflagellaris Peris-Felipo, sp. nov., S. magnioculis Peris-Felipo, sp. nov., and S. novateutoniae Peris-Felipo, sp. nov., are described and illustrated. The original combination for Synaldis ulmicola Ashmead, 188
Big and beautiful: the Megaxyela species (Hymenoptera, Xyelidae) of East Asia and North America
(2017)
Megaxyela Ashmead, 1898 comprises 13 species, four of which are described as new and one is removed from synonymy: Megaxyela euchroma Blank, Shinohara & Wei sp. nov. from China (Zheijang), M. fulvago Blank, Shinohara & Wei sp. nov. from China (Hunan, Jiangsu, Zhejiang), M. inversa Blank & D.R. Smith sp. nov. from the USA (West Virginia), M. langstoni Ross, 1936 sp. rev. from the eastern USA, and M. pulchra Blank, Shinohara & Sundukov sp. nov. from China (Hubei, Jilin, Liaoning, Shaanxi, Tibet), South Korea (Kangwon-do) and Russia (Primorskiy Kray). The male of M. parki Shinohara, 1992 is described for the first time. A lectotype is designated for M. gigantea Mocsáry, 1909. A cladogram, based on COI sequences of seven species, is presented and interpreted in view of selected morphological characters. Records of M. fulvago sp. nov. from Hunan and of M. pulchra sp. nov. from Tibet extend the known distribution of Megaxyela in the Old World 600 kilometers farther south and 2500 kilometers farther west than previous records.
A new species of the genus Teinobasis Kirby is described from the Muller Range in Western Province, Papua New Guinea. Its male is distinguished from all other Teinobasis species by having a pale labrum, an extensively bright orange thorax, and ventrally bowed superior anal appendages that are markedly shorter than the plump, apically rounded inferiors. Characters of the male are illustrated, and the affinities of the new species are discussed.
Species descriptions, keys to genera and species, and geographical distributions are presented for 43 species of the family Bruchidae (Coleoptera: Chrysomeloidea) for Chile. Of these species, seven are described as new:
Acanthoscelides aricae sp. nov., Lithraeus chillan sp. nov., L. comptus sp. nov., L. elguetai sp. nov., L. limari sp. nov., L. lonquimay sp. nov., and L. penai sp. nov. Eight species are endemic to Chile. A list of true host plants and floral records for those with known host associations is presented. Habitus photographs and drawings of pertinent body parts, including male genitalia, are provided. References pertaining to the previously described species are listed.
Many nomenclatural changes are implemented in the beetle families Georissidae, Histeridae, Hydraenidae, Hydrochidae, Hydrophilidae, Ptiliidae, Leiodidae and especially Staphylinidae, of the beetle series Staphyliniformia (Coleoptera), in preparation for making a world catalog of this group available online. Limited taxonomic changes are also made in the staphylinid subfamilies Osoriinae and Staphylininae.
At the level of family-group taxa, Article 29.4 of the current (1999) Zoological Code is reviewed and the original spellings of two tribal names, Nymphisterini Tishechkin (Histeridae) and Cryptonotopsisini Pace (Staphylinidae), are resurrected. The tribal name Stictocraniini Jakobson (Staphylinidae) is also resurrected as the valid name for its new synonym Fenderiini Scheerpeltz.
Changes at the genus-group level in Histeridae include placing Contipus Marseul as a new synonym of Hister Linnaeus due to the current placement of its validly designated type species C. subquadratus Marseul; proposal of Contipides Newton gen. nov. (type species Contipus digitatus Marseul) for the 10 species that had remained in Contipus of authors; and new designation of Idolia laevigata Lewis as type species of Idolia Lewis. In Ptiliidae, Rodwayia ovata Lea is newly designated as type species of Rodwayia Lea, and Throscidium germainii Matthews is newly designated as type species of Throscidium Matthews. In Staphylinidae, Paramichrotus Naomi is resurrected as a valid subgenus of Hesperosoma Scheerpeltz with Hemihesperosoma Hayashi placed as a new synonym of it; Sonoma corticina Casey is reaffi rmed as the type species of Sonoma Casey in place of Faronus tolulae LeConte; Stanosthetus Dejean is recognized as an available name and junior synonym of Euplectus Kirby; Taplandria Pace (type species T. guyanensis Pace) is recognized as a junior homonym and new synonym of Taplandria Pace (type species T. fl ava Pace); and Termitobiella Wasmann is resurrected as the valid name for the genus Felda Blackwelder. Replacement names for preoccupied generic or subgeneric names include in Histeridae Bellatricides Newton nom. nov. for Pachylister (Bellatrix) Mazur, junior homonym of Bellatrix Boie; and in Staphylinidae Foxiides Newton nom. nov. for Foxia Pace, junior homonym of Foxia Ashmead, and Xenasterides Newton nom. nov. for Xenaster Bierig, junior homonym of Xenaster Simonwitsch. Taxonomic changes at the generic level in Staphylinidae include proposal of Prolibia Newton gen. nov. (type species Lispinus californicus LeConte) for four Nearctic species recently placed in Clavilispinus Bernhauer; placement of Heterotrochinus Coiffait and its synonym Heterotrochus Coiffait as new synonyms of Eulibia Cameron; placement of the generic or subgeneric names Chapmaniella Bernhauer, Glenothorax Bierig, Euryolinus Bernhauer and Plesiolinus Bernhauer as new synonyms of Platydracus Thomson; and transfer of the subgenus Poikilodracus Scheerpeltz from Staphylinus Linnaeus to Platydracus. First reviser actions are used to select Georissites Ponomarenko (Georissidae) as the correct original spelling over the alternate original spelling Georyssites, and Kyrtusa Pace (Staphylinidae) as correct original spelling over Kirtusa.
Several hundred nomenclatural and taxonomic changes at the species group level are briefl y summarized here but are too numerous to list completely. Replacement names for preoccupied species or subspecies names in current use are proposed in Histeridae (3), Hydrochidae (1), Hydrophilidae (1), Leiodidae (2), Ptiliidae (3) and Staphylinidae (180); an additional staphylinid replacement name, Phloeopora nilgiriensis, is newly proposed by G. Paśnik. New or resurrected combinations are proposed for either nomenclatural or taxonomic reasons in the following genera (with indication of how many names in each genus): in Histeridae, Contipides Newton (10); in Staphylinidae, Abemus Mulsant and Rey (4), Allotrochus Fagel (6), Atheta Thomson (1), Cheilocolpus Solier (4), Eulibia Cameron (4), Foxiides Newton (1), Lispinus Erichson (3), Loncovilius Germain (2), Nacaeus Blackwelder (119), Naddia Fauvel (1), Neohypnus Coiffait and Sáiz (8), Neolosus Blackwelder (1), Ocypus Leach (2), Ontholestes Ganglbauer (1), Platydracus Thomson (59), Prolibia Newton (4) Termitobiella Wasmann (10), Thyreocephalus Guérin-Méneville (4), Xenasterides Newton (1), and Zeoleusis Steel (3). First reviser actions are used to resolve the correct original spellings (of two or more original spellings) of two species of Hydraena Kugelann (Hydraenidae) and 21 species of Staphylinidae. Changes in priority or availability of names are cited to establish the following names as valid over one or more new synonyms each: Acrotrichis rotundata (Haldeman) and Acrotrichis glabricollides Newton sp. nov. in Ptiliidae, Nemadiopsis franki Perreau in Leiodidae, and Gyrophaena nigra Kraatz, Heterothops fumigatus LeConte, Loncovilius germaini (Scheerpeltz), Philonthus upotovus Newton, sp. nov., Stenus fulviventris Rougemont, and nine species of Homalota Mannerheim in Staphylinidae. Finally, the species Eleusis lata Coiffait and Eleusis microlestiformis Coiffait are noted as not belonging to the genus Eleusis Laporte de Castelnau or to Staphylinidae, and are transferred without generic assignment to the subfamily Inopeplinae of the family Salpingidae.
A systematic redefinition of the species belonging to the genus Geomyphilus Gordon and Skelley, 2007 (Coleoptera: Scarabaeidae: Aphodiinae) of Mexico and neighboring countries is presented. The new species G. tuzincola of Mexico is described and figured. The new combination Coelotrachelus macgregori (Islas, 1955) is proposed.
This study reviews the taxonomy of the ant genus Nesomyrmex Wheeler, 1910 in the Afrotropical region. Previous revisionary studies are discussed and four species groups are proposed on the basis of external morphology. The N. angulatus group contains seven species that are widely distributed throughout the whole Afrotropical region, with one species also occurring in the Palaearctic and Malagasy regions. The N. cataulacoides group is monotypic, with one morphologically bizarre species found in Equatorial rain forests. The N. humerosus group is also monotypic and occurs in East Africa. The last and by far most species-rich group is the N. simoni group that contains 17 species, all of which are endemic to South Africa. The four groups are defined for the first time for the region, and an illustrated identification key is provided. Furthermore, the N. angulatus group is more thoroughly reviewed. One new species from Mozambique is described, N. inhaca sp. nov., and species accounts for the other six are provided. Also, an illustrated identification key to the species of the N. angulatus group is presented.
The genus Hybovalgus Kolbe, 1904 is represented by eight species on the Chinese mainland, many of which also inhabit northern Vietnam and Laos. Species of Hybovalgus are endemic to this area, and to the island of Taiwan. Until now, there is a lot of confusion in our knowledge of Hybovalgus on mainland China, due to erroneous descriptions of new species by European entomologists and incorrect identifications of specimens by local entomologists. Study of more material and many types has clarified this situation by better defining the species, synonymizing some of them, describing one new species, Hybovalgus calvus sp. nov. and recognizing the fact that females of two species were included in the new genus Excisivalgus Endrödi, 1952, which is here synonymized with Hybovalgus.
Haplosclerid sponges possessing a unique asymmetric flagelliform type of sigmoid microsclere have been reported from all global oceans. This peculiar spicule, characterized by a circular or elliptical shape, with a longer and sharper curved ending at one side and a shorter and more gradually curved ending at the opposing side, is proposed to be termed ‘flagellosigma’. These sponges invariably also possess smaller normal sigmas while their skeletal structure of oxea megascleres is markedly confused. They are assigned to the large genus Haliclona Grant, 1841 (family Chalinidae) in a new subgenus, Haliclona (Flagellia) subgen. nov. The species belonging to the new subgenus are reviewed and four species new to science are described, Haliclona (Flagellia) indonesiae subgen. et sp. nov., H. (F.) amirantensis subgen. et sp. nov., H. (F.) hiberniae subgen. et sp. nov. and H. (F.) hajdui subgen. et sp. nov. One species, H. (F.) hentscheli nom. nov., is given a new name on account of secondary homonymy caused by its transfer to the genus Haliclona. One species remains unnamed because of paucity of material. Already known species, reassigned to the new subgenus are H. (F.) hamata subgen. et comb. nov., H. (F.) flagellifera subgen. et comb. nov., H. (F.) porosa subgen. et comb. nov., H. (F.) edaphus subgen. et comb. nov. and H. (F.) anataria subgen. et comb. nov. Additional species are likely hiding among many erroneous records of ‘Gellius flagellifer’ from wide ranging parts of the global oceans.
The southeastern Australian millipede genus Pogonosternum Jeekel, 1965 is revised. Pogonosternum nigrovirgatum (Carl, 1902), P. adrianae Jeekel, 1982 and P. laetificum Jeekel, 1982 are redescribed; P. jeekeli Decker, sp. nov. and P. montanum Decker, sp. nov. are described from Victoria, New South Wales and Tasmania. P. nigrovirgatum infuscum Jeekel, 1982 and P. coniferum Jeekel, 1965 are junior synonyms of P. nigrovirgatum (Carl, 1902). An updated key to all five species of the genus is presented.
Fungivorous gall midges of the subfamilies Lestremiinae, Micromyinae, Winnertziinae and Porricondylinae were largely neglected in previous inventories of the Diptera faunas of the Czech and Slovak Republics. A taxonomic-faunistic study focusing on these subfamilies identified a total of 80 species, of which 49 are new records for the Czech Republic and 33 are new records for Slovakia. Species that have never before been found in central Europe are Aprionus dalarnensis Mamaev, 1998, A. oligodactylus Jaschhof, 2009, A. pigmentalis Mamaev, 1998, Asynapta inflata Spungis, 1988, Camptomyia gigantea Spungis, 1989, Cassidoides fulviventris (Mamaev, 1964), Claspettomyia hamata (Felt, 1907), Dendrepidosis longipennis (Spungis, 1981), Dicerura dispersa Jaschhof, 2013, Divellepidosis lutescens (Spungis, 1981), D. pallescens (Panelius, 1965), D. vulgata Jaschhof, 2013, Ekmanomyia svecica Jaschhof, 2013, Holoneurus ciliatus Kieffer, 1896, Monepidosis pectinatoides Jaschhof, 2013, Neocolpodia gukasiani (Mamaev, 1990), Neurolyga acuminata Jaschhof, 2009, Neurolyga interrupta Jaschhof, 2009, Parepidosis planistylata Jaschhof, 2013, Peromyia bidentata Berest, 1988, Porricondyla errabunda Mamaev, 2001, P. microgona Jaschhof, 2013, P. tetraschistica Mamaev, 1988, Schistoneurus irregularis Mamaev, 1964, Spungisomyia fenestrata Jaschhof, 2013, S. media (Spungis, 1981), Tetraneuromyia lamellata Spungis, 1987, T. lenticularis (Spungis, 1987), and Winnertzia parvispina Jaschhof, 2013. A new genus including a single new species of Porricondylini is described and named Glossostyles perspicua Jaschhof & Sikora gen. et sp. nov. on the basis of specimens collected in the Czech Republic and Sweden. Adult morphology suggests that Glossostyles gen. nov. is a close relative of Claspettomyia Grover, 1964.
Twelve new species are assigned to the genus Otitoma Jousseaume, 1898 in the family Pseudomelatomidae Morrison, 1966 and herein described: O. hadra sp. nov., O. neocaledonica sp. nov., O. rubiginostoma sp. nov and O. tropispira sp. nov. from New Caledonia; O. boucheti sp. nov., O. nereidum sp. nov. and O. sororcula sp. nov. from the Fiji Islands; O. xantholineata sp. nov. from the Solomon to the Fiji Islands; O. crassivaricosa sp. nov. from Fiji to Hiva Oa Island (Marquesas Archipelago); O. philpoppei sp. nov. from the Philippines but also reported from the Fiji Islands; O. elegans sp. nov. from the Fiji Islands and O. philippinensis sp. nov. from the Philippines. New data on O. carnicolor (Hervier, 1896) are provided. Otitoma mitra (Kilburn, 1986), from Southern Mozambique, is here considered a synonym of O. cyclophora (Deshayes, 1863). Drillia batjanensis Schepman, 1913, previously assigned to the genus Maoritomella Powell, 1942 in the family Borsoniidae Bellardi, 1875, is here assigned to the genus Otitoma. Photographs of the holotype of Drillia batjanensis are provided for the first time. In addition, color photographs of the type specimens of the following species are provided: Drillia kwandangensis Schepman, 1913, D. timorensis Schepman, 1913 and Mitrellatoma mitra Kilburn, 1986.
Contributions to the knowledge of the mite genus Stigmaeus Koch, 1836 (Acari: Stigmaeidae) of Turkey
(2017)
Based on the mite specimens collected within the scope of a study on Erzincan (Turkey) mite biodiversity, two species of the genus Stigmaeus are described and illustrated here: S. bifurcus sp. nov. as new to science and S. miandoabiensis Bagheri & Zarei, 2012 as a new record for Turkey. Some morphological abnormalities in the new species are noted. The deutonymph of S. miandoabiensis is described for the first time in this study. Discovery of this stage from soil and litter under Pinus sylvestris in Turkey adds more data to our knowledge of the species.
Ichneumonopsis Hardy,1973, a genus of oriental fruit flies, is revised and two new species, I. hancocki sp. nov. (from Peninsular Malaysia) and I. taiwanensis sp. nov. (from Taiwan), are described. A key to the three species of Ichneumonopsis is presented. In northern Thailand larvae of I. burmensis Hardy, 1973 develop in bamboo shoots of Pseudoxytenanthera albociliata (Munro) Nguyen and Dendrocalamus strictus (Roxburgh) Nees (Poaceae), not Melocalamus compactiflorus as previously reported. The recently discovered association of I. burmensis with bamboo substantiates our previous assumption assigning Ichneumonopsis to the primarily bamboo-inhabiting tribe Gastrozonini. Hence, we synonymize Ichneumonopsidini under Gastrozonini (syn. nov.).
The Chimarra lehibemavo species-group, new and endemic to Madagascar (Trichoptera, Philopotamidae)
(2017)
The Chimarra lehibemavo group is described to include thirteen new species: Chimarra lehibemavo sp. nov., C. cebegepi sp. nov., C. fenoevo sp. nov., C. forcellinii sp. nov., C. fotobohitra sp. nov., C. gattolliati sp. nov., C. gensonae sp. nov., C. jejyorum sp. nov., C. hamatra sp. nov., C. makiorum sp. nov., C. moramanga sp. nov., C. saha sp. nov. and C. tamara sp. nov. The adults are easily recognizable by their large size, yellow colour and the structure of the male genitalia. The membranous tergum IX and the absence of the mesal lobe of tergum X are observed in other lineages, but the strong asymmetrical deformation of the phallotheca is apomorphic. The group is monophyletic with unknown affinities, but a preliminary phylogenetic placement is suggested following genetic analysis of two specimens. With one exception, the species have restricted geographical distributions in Madagascar and inhabit rivers in eastern pristine rainforests.
Examination of leucothoid amphipods of the Red Sea has revealed seven species not previously reported from this location. Leucothoe minoculis sp. nov., Leucothoe pansa sp. nov., Leucothoe reimeri sp. nov., and Paranamixis sommelieri sp. nov. are described and the range of Leucothoe predenticulata Ledoyer, 1978, L. acutilobata Ledoyer, 1978 and L. squalidens Ledoyer, 1978 is expanded to include the Red Sea. Clarification of reports of L. acanthopus Schellenberg, 1928 and L. bannwarthi (Schellenberg, 1928) is provided and Leucothoe alani sp. nov. is described from outside the Red Sea.
We describe a new minute species of the genus Pristimantis, P. boucephalus sp. nov., from the Yanachaga-Chemillén National Park, Región Pasco, Peru. The description is based on a freshly collected male specimen found at 2950 m a.s.l. in a cloud forest and four previously unidentified museum specimens consisting of two adult males, one subadult female and a juvenile from the Yanachaga-Chemillén National Park. The new species is mainly characterized by a snout–vent length of 13.4–14.5 mm in adult males (n = 3), and 12.5 mm in the only known subadult female, and is compared morphologically and genetically with other taxonomically and biogeographically relevant species of Pristimantis. The new species is characterized by its small size, disproportionally large head with short snout, absence of a tympanic annulus and membrane, and reddish-copper iris. Phylogenetically it belongs to a speciose clade, an as yet unnamed species group, comprising both montane (Andes, Guiana Shield) and lowland (Amazon) taxa from the northern part of South America. The new species is genetically close to the sympatric P. cruciocularis. Species of Pristimantis occurring in the Cordillera Yanachaga region in the Andes of central Peru are members of six divergent phylogenetic lineages.
The genus Koiulus gen. nov. and its type-species, Koiulus interruptus gen. et sp. nov., are described from the Russian Far East. The new genus is compared with other genera of Mongoliulidae, in particular with Ussuriiulus Golovatch, 1980, also from the Russian Far East, with which it shares the absence of ozopores from individual body rings distributed along the body, a condition so far otherwise unknown in the superorder Juliformia. A synoptic table of genera and a list of species of Mongoliulidae are presented.
Japanese species of the genus Intybia are revised taxonomically, with the examination of the endophallic structure. Eight species, including one new species Intybia donan sp. nov. from Yonagunijima, are recognized. All species are described or redescribed with a key and figures. The endophallic structure contains one primary sclerite (gonoporal piece), three secondary sclerites (ligula, semigonoporal piece, and spinous plate) in some species, and a membranous basal area densely covered with many spines (spinous area). Based on the structures of the endophallus, the Japanese members of the genus are divided into two species groups (the histrio and pelegrini groups). The pelegrini species group is furthermore subdivided into three subgroups (subgroups 1–3). New distributional records are as follows: I. histrio from Hachijô-jima and Tanega-shima; I. niponica from Sakhalin and I. takaraensis from Tokuno-shima and Amami-Ôshima.
The Afrotropical planthopper genus Centromeriana Melichar, 1912 (Hemiptera, Fulgoromorpha, Dictyopharidae, Dictyopharinae, Orthopagini) is revised. Four species are included: C. jocosa (Gerstaecker, 1895) (the type species, with confirmed records from Cameroon, Equatorial Guinea and Gabon), C. lindbergae sp. nov. (described from Sierra Leone), C. rhinoceros sp. nov. (described from Togo) and C. simplex Melichar, 1912 (so far only known from Equatorial Guinea, Bioko island). Lectotypes are designated for C. jocosa and C. simplex and both species are redescribed including habitus photographs and detailed illustrations of the male and female genitalia which are published for the first time. A key for identification of the species of Centromeriana is provided. As far as known, the genus is endemic to the (Guineo-)Congolian region of western Africa.
A new genus is erected within the Cetoniini to describe a newly discovered species with characters shared between Heteroclita Burmeister, 1842, Ichnestoma Gory & Percheron, 1833 and Meridioclita Krikken, 1982. Neoclita pringlei gen. et sp. nov. exhibits a simple clypeal structure without specialized armour, along with hypertrophic and hairy tarsal segments as well as a fully winged female. The new species also exhibits an aedeagal structure closest to Meridioclita, with dorsal lobes of parameres substantially narrower than the ventral ones. The species appears to be restricted to high altitudes in the southwestern peri-Drakensberg area of the Eastern Cape Province, South Africa. Similarly to other mountain relicts known from the southern African region, adults emerge only after major rainfall events during the late spring to early summer season and do not show any evidence of feeding. It appears that flying activity may be temporarily interrupted following soil desiccation, to resume promptly after the next rainfall.
In this work we present a revision of the genus Ommatoiulus Latzel, 1884 in Portugal. Based on recently collected material and older museum samples, including type specimens, we describe six new species to science, viz. Ommatoiulus alacygni sp. nov., O. camurus sp. nov., O. denticulatus sp. nov., O. litoralis sp. nov., O. staglae sp. nov. and O. stellaris sp. nov. The species O. alacygni sp. nov., O. denticulatus sp. nov. and O. staglae sp. nov. described from the Algarve are outstanding by their extremely reduced mesomerital process. The species O. porathi (Verhoeff, 1893) and O. andalusius (Attems, 1927) are recorded and redescribed for the first time after their original description. The finding of O. andalusius – originally described from Andalusia in Spain – constitutes a new record for Portugal together with two species, viz. O. fuentei (Brolemann, 1920) and O. martensi Mauriès, 1969. The taxonomic status of several species is revised. Thus Archiulus (Schistocoxitus) cingulatus Attems, 1927 is here considered as a junior synonym of Ommatoiulus lusitanus (Verhoeff, 1895) while Schizophyllum cervinum Verhoeff, 1910 is synonymized with Ommatoiulus moreleti (Lucas, 1860). An identification key to all hitherto known Portuguese species of Ommatoiulus is presented as well as a distribution map illustrating the various species occurrences in the country.
Two new genera and species of tiger beetles from Baltic amber (Coleoptera: Carabidae: Cicindelinae)
(2017)
Two fossil tiger beetle species (Coleoptera, Carabidae, Cicindelinae) are described from Eocene Baltic amber using light microscopic and X-ray microscopic techniques. Both species are considered representatives of the subtribe Iresina Rivalier, 1971 due to the shared combination of character states: glabrous head, six labral and four suborbital setae, and glabrous pronotum. Palaeopronyssiformia groehni Wiesner, Will, and Schmidt, new genus, new species, is characterized by a glabrous and furrowed head with six labral setae, large eyes, presence of two supraorbital setae on each side, mandibles with two teeth of the incisor region, and a glabrous and furrowed pronotum. Palaeoiresina cassolai Wiesner, Will, and Schmidt, new genus, new species, is characterized by a unicolored, undentated labrum, mandibles with two teeth of the incisor region, glabrous head with six labral setae, two clypeal setae, two supraorbital setae on each side, and a glabrous pronotum, mesepisternum, mesepimeron, and metepisternum. The species described here represent the only known tiger beetle fossils preserved in Baltic amber.
From a moss sample collected in the Manabí Province in Ecuador, we extracted 96 specimens of a new species of eutardigrade. No eggs were found. In order to obtain eggs, an in vitro culture was prepared. In total, 136 specimens (including ten simplex), one exuvia and 44 eggs (including two with embryos) of the new species were obtained. In addition to the traditional taxonomic description with morphometrics, light and scanning microscopy imaging, we also provide nucleotide sequences of three nuclear (18S rRNA, 28S rRNA, ITS-2) and one mitochondrial (COI) DNA fragments of the new species. Macrobiotus polypiformis sp. nov. belongs to the hufelandi group and is most similar to Ma. paulinae Stec, Smolak, Kaczmarek & Michalczyk, 2015, but differs from it mainly by the lack of dorso-lateral patches of granulation on the cuticle, egg processes with longer and more numerous filaments and in some morphometric characters of both eggs and adults. Moreover, we provide a short discussion on the modifications/abnormalities of the claws in eutardigrades and the possible consequences on the taxonomic status of Mesobiotus armatus (Pilato & Binda, 1996), suggesting its consideration as species inquirenda (with uncertain taxonomic status).