Refine
Year of publication
Document Type
- Part of Periodical (11)
- Article (10)
- Book (1)
Language
- English (22)
Has Fulltext
- yes (22) (remove)
Is part of the Bibliography
- no (22) (remove)
Keywords
- new combinations (22) (remove)
Type specimens of Oedionychina Chapuis, 1875 described by Fabricius from the Kiel collection are examined and illustrated. Lectotypes are designated for the following species: Chrysomela albicollis Fabricius, 1787; Chrysomela nobilitata Fabricius, 1787; Chrysomela quadrifasciata Fabricius, 1787; Chrysomela quadriguttata Fabricius, 1781; Galleruca atomaria Fabricius, 1801; Galleruca decemguttata Fabricius, 1801; Galleruca fasciata Fabricius, 1798; Galleruca humeralis Fabricius, 1801; Galleruca lunata Fabricius, 1801; Galleruca nitida Fabricius, 1801; Galleruca obsoleta Fabricius, 1801; Galleruca petaurista Fabricius, 1801; Galleruca quadrinotata Fabricius, 1798; Galleruca sellata Fabricius, 1801. The species status is restored for Chrysomela quadriguttata Fabricius, 1781 and Alagoasa areata (Germar, 1824) comb. nov. The following new combinations are proposed: Phenrica quadriguttata (Fabricius, 1781), Asphaera nitida (Fabricius, 1801), Phenrica obsoleta (Fabricius, 1801), Alagoasa areata areata (Germar, 1824), Alagoasa areata decempunctata (Latreille, 1833), Alagoasa areata escuintla Bechyné, 1955, Alagoasa areata macromela Bechyné, 1958, Alagoasa areata praecessa Bechyné, 1959, Alagoasa areata recuperata Bechyné, 1959; all comb. nov. New placement: Galleruca avicenniae Fabricius, 1792 is removed from Alticini and placed in Galerucini incertae sedis; Galleruca trifasciata Fabricius, 1801 is removed from Chrysomelidae and placed in genus Ora Clark, 1865 (Scirtidae Fleming, 1821).
We simultaneously considered morphology and molecular phylogeny to modify the generic classification of the ‘pyropterine clade’ (Lycidae, Erotinae, Dictyopterini). To place species previously included in Benibotarus Kôno, 1932 in reciprocally monophyletic genera, we propose Gomezzuritus gen. nov. with the type-species Dictyopterus alternatus Fairmaire, 1856. Further, we transfer Gomezzuritus alternatus (Fairmaire, 1856) comb. nov., G. longicornis (Reiche, 1878) comb. nov., and G. rubripes (Pic, 1897) comb. nov. from Benibotarus to Gomezzuritus gen. nov. The pyropterine clade contains five genera in the Palaearctic region: Pyropterus Mulsant, 1838, Gomezzuritus gen. nov., Helcophorus Fairmaire, 1891, Greenarus Kazantsev, 1995, and Benibotarus Kôno, 1932. The arrangement of longitudinal elytral costae proved misleading for consideration of relationships. Two genera in distant positions share only four primary costae (Pyropterus and Helcophorus), and three similarly distant genera share the shortened primary costa 3, resulting in three primary and four secondary longitudinal costae (Gomezzuritus, Greenarus, and Benibotarus). The larva of Gomezzuritus alternatus is described in detail, and it is compared with the larvae of other Dictyopterini, including the presumed larva of G. longicornis.
An annotated list, including information on type species, distribution, and number of species, is provided for all of the non-flea-beetle galerucine genera known to occur in the New World (tribes Galerucini, Metacyclini, and Luperini). A diagnostic key to the genera is provided. Habitus illustrations are provided for most genera. The following new genera are proposed: Amplioluperus gen. nov., Cornuventer gen. nov., Geethaluperus gen. nov., Megarhabda gen. nov., Mexiluperus gen. nov., Monoaster gen. nov., Pyesexora gen. nov., Texiluperus gen. nov., Trachyelytron gen. nov. and Yingabruxia gen. nov. The following new taxonomic placements are proposed: Microbrotica Jacoby, 1887 is transferred from the tribe Metacyclini to the section Diabroticites Chapuis, 1875 (tribe Luperini, subtribe Diabroticina Chapuis, 1875); Pteleon Jacoby, 1888 is transferred from the section Exosomites Wilcox, 1973 (tribe Luperini, subtribe Luperina Gistel, 1848) to the section Scelidites Chapuis, 1875 (subtribe Luperina). The following new combinations are proposed: Luperodes histrio Horn, 1895, Luperus maculicollis LeConte, 1884, and Scelolyperus cyanellus Horn, 1895 are transferred from Pseudoluperus Beller & Hatch, 1932 to Amplioluperus; Luperodes tuberculatus Blake, 1942 is transferred from Pseudoluperus to Cornuventer; Luperus flavofemoratus Jacoby, 1888 is transferred from Pseudoluperus to Geethaluperus; Trirhabda obscurovittata Jacoby, 1886 is transferred from Trirhabda LeConte, 1865 to Megarhabda; Cneorane nigripes Allard, 1889 is transferred from Scelida Chapuis, 1875 to Metacycla Baly, 1861; Luperodes wickhami Horn, 1893 and Luperus dissimilis Jacoby, 1888 are transferred from Pseudoluperus to Mexiluperus; Scelolyperus tenuimarginatus Bowditch, 1925, is transferred from Scelida to Mimastra Baly, 1865 and is synonymized with Mimastra semimarginata Jacoby, 1886 syn. nov.; Pseudoluperus fulgidus Wilcox, 1965 and Pseudoluperus linus Wilcox, 1965 are transferred from Pseudoluperus to Monoaster; Crioceris detrita detrita Fabricius, 1801, Malacosoma detrita laevicollis Jacoby, 1887, Pyesia detrita meridionalis Bechyné, 1958, Pyesia elytropleuralis elytropleuralis Bechyné, 1958, and Pyesia elytropleuralis subalutacea Bechyné, 1958 are transferred from Pyesia Clark, 1865 to Pyesexora; Luperodes spretus Horn, 1893 and Luperodes texanus Horn, 1893 are transferred from Pseudoluperus to Texiluperus; Chthoneis smaragdipennis Jacoby, 1888 is transferred from Platymorpha Jacoby, 1888 to Trachyelytron; Luperus albomarginatus Jacoby, 1888 is transferred from Pseudoluperus to Trichobrotica Bechyné, 1956; and Galleruca sordida LeConte, 1858, Monoxia apicalis Blake, 1939, Monoxia batisia Blatchley, 1917, and Monoxia brisleyi Blake, 1939 are transferred from Monoxia LeConte, 1865 to Yingabruxia; all comb. nov. Pseudoluperus decipiens (Horn, 1893), originally described in Scelolyperus Crotch, 1874, is reduced to a junior synonym of Pseudoluperus longulus (LeConte, 1857), syn. nov. Trachyscelida dichroma Viswajyothi & Clark is proposed as a nom. nov. for Racenisa bicolor Bechyné, 1958 (not Agelastica bicolor LeConte, 1884), as both species are currently placed in the genus Trachyscelida Horn, 1893.
The present study aims to resolve the taxonomic confusion involving several taxa within Mycetophagidae Leach, 1815, originating from the introduction of the genus Atritomus Reitter, 1877, and then by its subsequent controversial interpretation. A detailed overview of the taxonomic and nomenclatural history of the taxa previously linked to Atritomus is provided. The authors propose the introduction of Stereophilus Biscaccianti, Audisio & Esser gen. nov. for Atritomus filicornis Reitter, 1887, and the restoration of Entoxylon Ancey, 1869 at the genus rank, together with some rectifications regarding the authorship and the date of publication of both Entoxylon and its type species, E. abeillei Ancey, 1869. Moreover, the Ethiopian species Atritomus vicinus Grouvelle, 1908 is herein transferred to the genus Typhaeola Ganglbauer, 1899 based on the examination of the holotype. The following new combinations are proposed: Entoxylon baudii (Seidlitz, 1889) comb. nov. (from Esarcus Reiche, 1864), Entoxylon besucheti (Dajoz, 1964) comb. nov. (from Esarcus subg. Entoxylon), Entoxylon franzi (Dajoz, 1964) comb. nov. (from Esarcus subg. Entoxylon), Entoxylon inexpectatus (Dajoz, 1964) comb. nov. (from Esarcus subg. Entoxylon), Entoxylon martini (Reitter, 1887) comb. nov. (from Esarcus), Stereophilus filicornis (Reitter, 1887) gen. et comb. nov. (from Atritomus), Typhaeola vicina (Grouvelle, 1908) comb. nov. (from Atritomus).
This paper deals with the brachypterous Meconematini, including three new genera, Acosmetides gen. nov., Neocyrtopsides gen. nov. and Macrocosmetura gen. nov. Five new species are described: Acosmetides peltates gen. et sp. nov., Acosmetides dilobosa gen. et sp. nov., Acosmetides platycerca gen. et sp. nov., Neocyrtopsides bispina gen. et sp. nov. and Macrocosmetura truncata gen. et sp. nov. Two new combinations are proposed: Acosmetides trigentis (Wang, Bian & Shi, 2016) gen. et comb. nov. and Neocyrtopsides platycata (Shi & Zheng, 1994) gen. et comb. nov.
The classification of the superfamily Psylloidea is revised to incorporate findings from recent molecular studies, and to integrate a reassessment of monophyla primarily based on molecular data with morphological evidence and previous classifications. We incorporate a reinterpretation of relevant morphology in the light of the molecular findings and discuss conflicts with respect to different data sources and sampling strategies. Seven families are recognised of which four (Calophyidae, Carsidaridae, Mastigimatidae and Triozidae) are strongly supported, and three (Aphalaridae, Liviidae and Psyllidae) weakly or moderately supported. Although the revised classification is mostly similar to those recognised by recent authors, there are some notable differences, such as Diaphorina and Katacephala which are transferred from Liviidae to Psyllidae. Five new subfamilies and one new genus are described, and one secondary homonym is replaced by a new species name. A new or revised status is proposed for one family, four subfamilies, four tribes, seven subtribes and five genera. One tribe and eight genera / subgenera are synonymised, and 32 new and six revised species combinations are proposed. All recognised genera of Psylloidea (extant and fossil) are assigned to family level taxa, except for one which is considered a nomen dubium.
The species of Stenothemus Bourgeois, 1907 from Southeast China are reviewed. Stenothemus fukienensis Wittmer, 1974 and S. kuatunensis Wittmer, 1979 are supplementarily described. Two new species are described, S. longicornis Y. Yang & H. Liu sp. nov. (China: Guangdong) and S. flavus Y. Yang & X. Yang sp. nov. (China: Zhejiang). Five new combinations are established: S. biimpressiceps (Pic, 1930) comb. nov. (from Cantharis L.), S. chinensis (Wittmer, 1982) comb. nov., S. limbatipennis (Pic, 1926) stat. rev. et comb. nov., S. nigriceps (Wittmer, 1955) comb. nov. and S. pallicolor (Wittmer, 1951) comb. nov. (from Lycocerus Gorham). Leiothorax atrosanguineus Švihla, 2005 syn. nov. is synonymized with S. chinensis, Lycocerus limatus Kazantsev, 2007 syn. nov. with S. limbatipennis. The above species are illustrated with habitus photos, aedeagi, abdominal sternites VIII and internal genitalia of female. A key for the identification of the above species is provided.
Neofidia Strother nom. nov., is proposed as the replacement name for Fidia Baly, 1863, a junior homonym of Fidia Motschulsky, 1861 (not 1860, Griffin 1936). A list of the included species of Neofidia Strother nom. nov. and Fidia Motschulsky, 1861 is provided for clarity. Fidia medvedevi nom. nov. is the new replacement name proposed for Lypesthes vietnamicus Medvedev, 2015. Fidia kanaraensis (Jacoby, 1895) is redescribed and habitus, male and female genitalia are figured. Cashew (Anacardium occidentale L.) is reported as a new host of F. kanaraensis and partial information on the life history is provided. Eggs are laid singly on the surface of soil, and are covered with excreta and soil. Larvae tunnel into the tender roots. Adults are nocturnal and feed on tender leaves.
Five new species of Peltonotellini (Caliscelinae) are described and illustrated: Bruchomorpha pseudodorsata sp. nov., Fitchiella brachyrhina sp. nov., Protrocha nigrilutea sp. nov. and P. punctatosa sp. nov. from Mexico, and Fitchiella zahniseri sp. nov. from Panama. Additionally, five previously described species are redescribed based on newly collected specimens: Aphelonema brevata Caldwell, 1945 (proposed original combination), Bruchomorpha decorata Metcalf, 1923, Bruchomorpha mormo Kirkaldy, 1907, Nenema virgata (Doering, 1941) and Protrocha nesolitaria (Caldwell, 1945). Bruchomorpha decorata is recorded from Panama for the first time. Redescriptions provide new information on the distribution of sensory pits and the first detailed descriptions of male and female terminalia for these species.
Olpidiopsis is a genus of obligate holocarpic endobiotic oomycetes. Most of the species classified in the genus are known only from their morphology and life cycle, and a few have been examined for their ultrastructure or molecular phylogeny. However, the taxonomic placement of all sequenced species is provisional, as no sequence data are available for the type species, O. saprolegniae, to consolidate the taxonomy of species currently placed in the genus. Thus, efforts were undertaken to isolate O. saprolegniae from its type host, Saprolegnia parasitica and to infer its phylogenetic placement based on 18S rDNA sequences. As most species of Olpidiopsis for which sequence data are available are from rhodophyte hosts, we have also isolated the type species of the rhodophyte-parasitic genus Pontisma, P. lagenidioides and obtained partial 18S rDNA sequences. Phylogenetic reconstructions in the current study revealed that O. saprolegniae from Saprolegnia parasitica forms a monophyletic group with a morphologically similar isolate from S. ferax, and a morphologically and phylogenetically more divergent species from S. terrestris. However, they were widely separated from a monophyletic, yet unsupported clade containing P. lagenidioides and red algal parasites previously classified in Olpidiopsis. Consequently, all holocarpic parasites in red algae should be considered to be members of the genus Pontisma as previously suggested by some researchers. In addition, a new species of Olpidiopsis, O. parthenogenetica is introduced to accommodate the pathogen of S. terrestris.