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An overview of the genus Psephenops Grouvelle (Coleoptera: Psephenidae: Psepheninae) is provided with geographic distributions of the species. The taxonomic history of Psephenops smithi Grouvelle, the type species from Grenada and St. Vincent, and junior synonym Xexanchorinus latus Grouvelle from Grenada, is discussed, and lectotypes and paralectotypes are designated for both. Photographs of the type series and a non-type specimen with illustrated male genitalia, along with new distributional information for the species, are provided. The male, female, and associated larva of Psephenops trini Barr and Shepard, new species, are described and illustrated, as is the habitat of this species in Trinidad and Tobago. The Peruvian species Psephenus robacki Spangler is transferred from Psephenus Haldeman to Psephenops as Psephenops robacki (Spangler) new combination. Photographs of the female holotype are included, and possible new distributional records from Peru are reported.
ZooBank registration. urn:lsid:zoobank.org:pub:5C9ECB63-6A77-4FF6-8391-BF0F77BE5674
Though recent investigations have contributed substantially to our understanding of the Alpine-Dinaric radiation of the genus Zospeum Bourguignat, 1856, its southernmost member, Zospeum troglobalcanicum Absolon, 1916, has remained a taxonomic ghost. The assumed absence of type material, the insufficient original description, and the lack of new samples from its Western Balkan type locality have stymied further clarification. The recent discovery of a single syntype shell housed at the Natural History Museum Vienna now enables the first morphological assessment via 3D X-ray and SEM imaging. Based on this image data, different characters for assessing the southernmost members of the genus are determined and a lectotype is designated. Eleven allied species from 15 Western Balkan populations are described from museum material and recent sampling efforts: Z. amplioscutum Jochum & Ruthensteiner sp. nov., Z. biokovoense Jochum & Ruthensteiner sp. nov., Z. constrictum Jochum & Ruthensteiner sp. nov., Z. dubokidoense Jochum & Ruthensteiner sp. nov., Z. intermedium Jochum & Ruthensteiner sp. nov., Z. kolbae Jochum, Inäbnit, Kneubühler & Ruthensteiner sp. nov., Z. neuberti Jochum & Ruthensteiner sp. nov., Z. njegusiense Jochum & Ruthensteiner sp. nov., Z. njunjicae Jochum, Schilthuizen & Ruthensteiner sp. nov., Z. tortuosum Jochum & Ruthensteiner sp. nov. and Z. tumidum Jochum, Schilthuizen & Ruthensteiner sp. nov. One species, Z. kolbae, is described using DNA sequence data and one species, Z. simplex Inäbnit, Jochum & Neubert, 2021 for which DNA sequence data is already available, is supported by morphological data presented in this study. The DNA sequence dataset (COI, 16S and H3) is included here and implemented in the most recent phylogenetic reconstruction of the genus. A translation of Karel Absolon’s notes from the Balkan scientific expeditions is provided.
Taxonomic revision of the African assassin bug genus Fusius (Heteroptera: Reduviidae: Peiratinae)
(2023)
The African assassin bug genus Fusius Stål, 1862 is revised after the examination of type specimens with redescriptions of four species. Lectotypes of Pirates (Fusius) H-flavum Reuter, 1881 and Pirates rubricosus Stål, 1855 are designated. The status of P. (Fusius) H-flavum Reuter, 1881 is revalidated with its current name as F. hflavus (Reuter, 1881) stat. rev. et comb. nov. Seven new synonyms are proposed: F. dilutus Miller, 1957 = F. gowdeyi Miller, 1957 syn. nov. = F. liberiensis Miller, 1957 syn. nov. = F. dilutus anonymus Dispons, 1969 syn. nov. = F. dilutus vicinus Dispons, 1969 syn. nov.; F. distinctus Miller, 1957 = F. sylvestris Miller, 1957 syn. nov.; F. hflavus (Reuter, 1881) = F. hargreavesi Miller, 1957 syn. nov.; F. rubricosus (Stål, 1855) = F. ugandensis Miller, 1957 syn. nov. A key is provided to separate the four species of this genus. Diagnosis and distribution of Fusius are briefly discussed.
The species of Aphaniosoma Becker, 1903 described from Egypt by Collin in 1949 are reviewed and lectotypes designated for Aphaniosoma creperum Collin, 1949, A. fissum Collin, 1949, A. lamellatum Collin, 1949 and A. sodalis Collin, 1949. All species known from the eastern Mediterranean and the Middle East are reviewed, with annotations, distributions and a key to species. The following 19 species are described as new and illustrated: A. acitergum sp. nov., A. aegyptium sp. nov., A. angulitergum sp. nov., A. captiosum sp. nov., A. cristatum sp. nov., A. curvistylus sp. nov., A. daedalum sp. nov., A. denticulosum sp. nov., A. flavipyga sp. nov., A. freidbergi sp. nov., A. interispina sp. nov., A. kravchenkoi sp. nov., A. longilingua sp. nov., A. lucidum sp. nov., A. meltseri sp. nov., A. miricercus sp. nov., A. palestinense sp. nov., A. praeditum sp. nov. and A. yaromi sp. nov. Biology and ecology are commented upon.
The genus Zingiber contains about 180 species distributed mainly in tropical regions. Several species of Zingiber are cultivated globally for their medicinal and culinary value, such as true gingers (Z. officinale), bitter gingers (Z. zerumbet), and Z. purpureum. In Taiwan, two endemic species and one incompletely known taxon were recorded in the last edition of Flora of Taiwan, and several taxonomic issues still remain unresolved. Therefore, we revised the Taiwanese Zingiber based on morphological, palynological, anatomical, and molecular evidence, as well as their distribution. The results showed that floral characters such as labellum, fertile bracts, and corolla tubes are of great taxonomic value in distinguishing taxa of Zingiber of Taiwan. Accordingly, five species are treated in the present study, namely Z. chengii Y.H.Tseng, C.M.Wang & Y.C.Lin, Z. mioga Thunb., Z. oligophyllum K.Schum., Z. pleiostachyum K.Schum., and Z. shuanglongense C.L.Yeh & S.W.Chung. Zingiber mioga might be a newly naturalized species to Taiwan. Zingiber kawagoii Hayata and Z. koshunense C.T.Moo are treated as synonyms of Z. pleiostachyum.
Arcola malloi (Pastrana, 1961) is a junior subjective synonym of Macrorrhinia endonephele (Hampson, 1918) syn. nov. (Lepidoptera: Pyralidae). The species is a biological control agent introduced in United States and Australia to control alligatorweed, Alternanthera philoxeroides (Mart.) Griseb. (Amaranthaceae). The synonymy is recognized by comparison of type specimens, genitalic dissections, and DNA COI barcoding. Vogtia Pastrana, 1961 syn. nov. and Arcola Shaffer, 1995 syn. nov. are synonymized with Macrorrhinia Ragonot, 1887. Macror-rhinia megajuxta (Neunzig and Goodson, 1992) comb. nov. is transferred from Ocala Hulst, 1892. Lectotypes are designated for Divitiaca ochrella Barnes and McDunnough, 1913, and Divitiaca simulella Barnes and Mc-Dunnough, 1913.
The genus Ochodaeus in Italy: taxonomy and distribution (Coleoptera: Scarabaeoidea: Ochodaeidae)
(2020)
The author provides a taxonomic, nomenclatural and distributional review of the genus Ochodaeus Dejean, 1821 (Coleoptera: Scarabaeoidea: Ochodaeidae) in Italy. All Italian populations have been confirmed to belong to a single species, O. chrysomeloides (Schrank, 1781). After the study of a syntype, O. cychramoides Reitter, 1892, formerly considered an Italian endemic, is confirmed to be a junior synonym of O.chrysomeloides. Type material of O. chrysomeloides is believed to be destroyed, therefore a neotype is here designated and deposited at the Natural History Museum of Vienna, Austria. A lectotype is here designated for O. cychramoides and deposited in the Hungarian Natural History Museum of Budapest, Hungary. The Italian distribution of O. chrysomeloides is given in detail and illustrated by a map.
Nisitrus Saussure, 1878 is a diurnal and monophyletic group of eneopterine crickets found in parts of Southeast Asia. Species often have vivid colourations which make them charismatic photograph subjects among macro photographers. However, their taxonomy has not been revised since their original descriptions, whereas there are also species awaiting to be discovered and described. A synoptic revision is therefore needed prior to studying the phylogenetic relationships of the genus, and before undertaking more precise studies on biogeography and evolution of traits. By holistically incorporating information about general morphology, male and female genitalia, and bioacoustics, we revise the taxonomy of these crickets and recognise 10 valid species of Nisitrus. Five new species are described: N. crucius Robillard & Tan sp. nov. from Borneo; N. danum Robillard & Tan sp. nov. from Borneo; N. hughtani Robillard & Tan sp. nov. from Sumatra; N. malaya Robillard & Tan sp. nov. from Malay Peninsula; and N. rindu Robillard & Tan sp. nov. from Borneo. We redescribe N. brunnerianus and N. insignis; describe the calls of N. malaya sp. nov., N. musicus and N. vittatus. We consider N. sumatrensis as a junior synonym of N. insignis; and N. marginata as a junior synonym of N. vittatus. Nisitrus hyalinus requires further revision. We also consider N. maculosus as a dubious name.
Many early taxonomic works on North American bees were published by Europeans using specimens collected in the New World, some with type locations so imprecise that uncertainty on the nomenclatural status remains to this day. Two examples come from Fabricius (1745–1808) who described Andrena virescens Fabricius, 1775 and Apis viridula Fabricius, 1793 from “America” and “Boreal America”, respectively. The former species of Agapostemon Guérin-Méneville, 1844 occurs across most of the United States and southern Canada, the latter presumed an endemic to Cuba. The type materials of these two taxa have never been compared to each other, though a morphology-based phylogenetic analysis placed both in distinct species groups. Here we synonymize Apis viridula under Ag. virescens, thereby making Ag. femoralis (Guérin-Méneville, 1844) available as the name for the Cuban species. A lectotype for Ag. femoralis (the type species for the genus Agapostemon) is hereby designated to stabilize this taxonomy. We also synonymize Ag. obscuratus Cresson, 1869 under Ag. femoralis, suggesting that it represents a dark colour polymorphism. As Ag. cubensis Roberts, 1972 is a junior secondary homonym of Ag. cubensis (Spinola, 1851), we offer Ag. robertsi as a replacement name for the former.