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... Falsocis Pic is a distinct genus, which seems to be restricted to the Neotropical Region. Falsocis opacus Pic and the subspecies Falsocis opacus flavus Pic were originally described from French Guiana (Pic 1916(Pic , 1922, but the species also occurs in northern Brazil. Blackwelder (1945) and Abdullah (1973) referred to this genus as "Falcocis" and "Falcosis", respectively, and derived the specific and subspecific epithets as the genus name were feminine. ...
... 30.1.2). Since the works of Pic (1916Pic ( , 1922, and the citations of Blackwelder (1945) and Abdullah (1973), few references to the genus are found in the literature. Lawrence (2001) informally cited the genus to Costa Rica. ...
... Unfortunately, most of the primary types of Brazilian ciids are deposited in institutions outside of Brazil (mainly in European museums), and some are even lost (e.g. the types of Trichapus Friedenreich; see Lawrence 1987). The primary types of Brazilian species described by Lawrence (1987), and the ones described by my colleagues and I Lopes-Andrade & Zacaro 2003a, b;Lopes-Andrade et al. 2003;Almeida & Lopes-Andrade 2004;Lopes-Andrade & Lawrence 2005) Pic, 1916 Falsocis opacus flavus Pic, 1922 Falsocis brasiliensis sp. nov. ...
Article
The genus Falsocis Pic is redescribed based on F. opacus Pic and F. brasiliensis sp. nov. an endangered Brazilian species. A key to males of the species of Falsocis is provided, together with a description of the external morphology of adults and of the morphology of male genitalia of both species. In addition, the female genitalia of F. brasiliensis sp. nov. are described. Falsocis is included in the tribe Ciini, and its relationship with Acanthocis Miyatake and other Ciidae genera is discussed. Falsocis brasiliensis sp. nov. is known from only three Atlantic Forest remnants, all surrounded by urban areas, pastures or agriculture, and is probably one of the most endangered Brazilian ciids.
... This placement to be considered tentative. (Pic, 1911) (Fig. 34) = Anthicus pietschmi Pic, 1938Anthicus luristanicus Pic, 1911b. Anthicus Pietschmi Pic, 1938: 11 (description . ...
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Description of 3 new species in collaboration with Telnov D., within the work: Telnov 2022. Revisional notes on the genus Microhoria Chevrolat, 1877 (Insecta: Coleoptera: Anthicidae) from the Eastern Mediterranean and Turkey, with new descriptions, an annotated catalogue, and a key. Baltic J. Coleopterol., 22(2): 195–312
... This placement to be considered tentative. (Pic, 1911) (Fig. 34) = Anthicus pietschmi Pic, 1938Anthicus luristanicus Pic, 1911b. Anthicus Pietschmi Pic, 1938: 11 (description (Fig. 35, 55B-C) urn:lsid:zoobank.org:act:82BF1EFA-DDFB-442D-B93B-EC44CB15998B ...
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The species of Microhoria Chevrolat, 1877 from the Eastern Mediterranean including Turkey and Sinai Peninsula, are reviewed, keyed, and catalogued for the first time. Status change is proposed for Microhoria rubronotata (Pic, 1896) stat. nov. New synonyms are proposed for Microhoria emaciata (Pic, 1896) (= Anthicus leuthneri var. creticus Pic, 1903 syn. nov.), M. latipennis (Pic, 1892) (= A. leuthneri var. dissimilis Pic, 1897 syn. nov.), M. ottomana (LaFerté-Sénectère, 1849) (= A. tenebricosus Pic, 1897 syn. nov.), and M. rubronotata (Pic, 1896) stat. nov. (= A. humerifer Pic, 1902 syn. nov.). Lectotypes are designated for the following 11 taxa: Microhoria akbesiana (Pic, 1896), M. angulapex (C. Koch, 1935), M. boyadjeani (Pic, 1904), M. corallicollis (Reitter, 1889), M. delagrangei (Pic, 1892), M. emaciata (Pic, 1896), M. inobscura (Pic, 1908), M. ionica (Pic, 1901), M. kaifensis (Pic, 1896), M. rubriceps (Pic, 1896), and M. schmiedeknechti (Pic, 1899). The following ten species new to science are described: Microhoria bremeri sp. nov., M. capreolus Telnov & Degiovanni sp. nov., M. janssoni sp. nov., M. machairodus Telnov & Degiovanni sp. nov., M. punctatissima sp. nov., M. quercus sp. nov., M. walkeri sp. nov. (all from Turkey), M. muehlei Telnov & Degiovanni sp. nov., M. orbitalis sp. nov. (both from Iran), and M. paxvobiscum sp. nov. (Iraq). Taxonomic status of Anthicus terminatus var. latebrunneus Pic, 1901 is discussed. Illustrations of numerous taxa are provided for the first time. In total, 41 species confirmed from the Eastern Mediterranean and records of another six species require further confirmation. In addition, several new faunistic records are provided.
... South India; Thailand; West Malaysia, East Malaysia; Indonesia: Sumatra, Mentawei; Brunei. (Pic, 1922) Heteroscapha tonkineum Pic, 1922: 1. Bironium tonkineum;Löbl, 1990: 616 (differential characters). ...
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The Asian species of Bironium are reviewed and three new species are described: B. lobatumsp. nov. and B. yunnanumsp. nov. from South China and B. sulcatumsp. nov. from Thailand. Bironium atripenne (Pic) and B. amicale Löbl are placed in synonymy with B. grouvellei (Achard) and B. elegans Löbl, respectively. Lectotypes are designated for B. atripenne (Pic), B. distinctum (Achard), B. grouvellei (Achard) and B. sumatranum (Achard). Redescriptions are provided for B. biplagatum (Achard), B. feai (Achard), B. grouvellei (Achard), B. minutum (Achard), B. nigrolineatum (Pic), B. rufonotatum (Pic), B. sumatranum (Achard), and B. tonkineum (Pic); otherwise, original descriptions are appended with new characters. New collecting records significantly expand the known distribution ranges of many species. A key to the Asian species is given. A cladistic analysis based 27 characters that included all but four species of Bironium (29 species) rooted with Baeocera and Birocera was poorly resolved but indicated that there were at least three dispersal events from mainland Asia east through Wallacea towards Papua New Guinea (PNG). One potential dispersal event is represented by a clade that includes an undescribed species from Sulawesi, and others that may have undergone subsequent vicariance. The PNG fauna is represented by two lineages, one dispersal that involves B. flavapex Löbl, the only known species from the Moluccas that is the sister taxon of B. maculatum Löbl from PNG and B. nepalense Löbl from Nepal; the other is a monophyletic lineage of PNG species placed within a paraphyletic group of mainly mainland Asian taxa.
... Diboma Thomson, 1864 Remarks: Thomson (1864) proposed the genus Diboma with the type species Diboma tranquilla Thomson, 1864 in the beetles family Cerambycidae. Unfortunately, the generic name was already preoccupied by Walker (1863) Pic, 1925;Donysia Gressitt, 1940 andSybrocentrura Breuning, 1947 are the junior synonyms of Diboma Thomson, 1864(Kusama & Takakuwa, 1984Heffern, 2005). So I propose to substitute name Zotalemimon Pic, 1925 that is available and the senior synonym of the generic name Diboma Thomson, 1864 for Diboma Thomson, 1864. ...
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A replacement name, Fehmii nom. nov. is proposed for the preoccupied genus name Damiria Fairmaire, 1900 (Cerambycidae: Cerambycinae: Cleomenini). Also, a clarification on the validity of the generic name Zotalemimon Pic, 1925 is presented. Remarks: The name Damiria was initially introduced by Keller (1891) for a genus of the sponges family Acarnidae (with the type species Damiria simplex Keller, 1891). For the present, Anisotylacanthaea Vacelet, 1969; [Damira] de Laubenfels (lapsus) and Xytopsene de Laubenfels, 1936 are the junior names of Damiria Keller, 1891 (Hooper, 2000). Subsequently, Fairmaire (1900) described a beetle genus of the family Cerambycidae (with the type species Damiria perrieri Fairmaire, 1900 by monotypy) under the same generic name. Thus, the genus Damiria Fairmaire, 1900 is a junior homonym of the genus Damiria Keller, 1891. According to Article 60 of the International Code of Zoological Nomenclature, I propose for the genus Damiria Fairmaire, 1900 the new replacement name Fehmii nom. nov. The name dedicated to Fehmi Özdikmen. The name is masculine in gender.
... Remarks. The new species is similar to Homoeogenus obscurum (Pic, 1923), Homoeogenus chinense Lee and Yang, 1993, and Homoeogenus maai Lee and Yang, 1997 from China, but can be distinguished by the following characteristics: body light brown and smaller; antennomeres 3 and 4 serrate, antennomeres 5e10 pectinate; apical maxillary palpomere elongate and slightly produced apically; apical labial palpomere stout, rounded anterior margin in lateral view produced apically; prosternal process slender, narrowing at apex; mesoventral process obtuse, blunt at apex. Penis more or less subparallel-sided, almost gradually tapering toward pointed apex. ...
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The water penny beetles (Coleoptera: Psephenidae) of the Korean Peninsula are reviewed based on their external morphology and mitochondrial cytochrome c oxidase subunit I gene sequences. Four subfamilies, four genera, and four species, including a new species described herein, are recognized: Eubrianax ramicornis Kiesenwetter, 1874 (Eubrianacinae), Homoeogenus coreanicum sp. nov. (Eubriinae), Malacopsephenoides japonicus (Masuda, 1935) (Psephenoidinae), and Mataeopsephus japonicus (Matsumura, 1916) (Psepheninae). The psephenid subfamily Eubriinae and the genus Homoeogenus Waterhouse, 1880 are here recorded from the Korean Peninsula for the first time. Analyses of the cytochrome c oxidase subunit I gene sequences of larvae and adults of the four Korean species produced a bootstrap support of 100% for each species. Descriptions, habitat data, habitus photographs, line-drawings of male genitalia, and keys to the adults and larvae of the Korean species of Psephenidae are provided.
... Hope, 1831: 28 -Nepaul;Gahan, 1906: 171 -Nepal;Heller, 1924a: 33 -Nepal;Weigel, 2006: 499 -Nepal;Weigel, 2010: 204 -Nepal;Niisato & Lin, 2013: 74, 81 -Nepal;Kariyanna et al., 2017: 74 -Nepal. nigriceps A. White, 1855: 181 (Heliomanes) inapicalis Pic, 1922a: 23 Weigel, 2006Weigel, 2010: 204 -Nepal;Niisato & Lin, 2013: 75, 81 -Nepal;Niisato & Yokoi, 2016: 41 -Nepal;Kariyanna et al., 2017: 74 -Nepal;"Dhankuta, east. Nepal -24.6.2013" ...
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The Catalogue includes all 505 Cerambycidae species of Nepal fauna known up to 2019 with the references to the original descriptions and regional records; 52 species are newly recorded for Nepal fauna.
... Corticeus subalutaceus(Pic, 1924). A. Habitus. ...
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A determination key of the 28 species of Corticeus of Madagascar, the Mascarene Islands and the Comores is outlined. Most of the species are illustrated and annotations on their distribution are provided. Key words. Coleoptera, Tenebrionidae, Hypophlaeini, Corticeus, Afrotropical Region, Madagascar, Comore Islands, La Réunion, Mauritius, determination key, illustration.
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Three species of the genus Plateros Bourgeois, 1879—P. manaliensis (Bocáková, 1997), P. atrosuturalis Kazantsev, 2011, and P. gavryushini Kazantsev, 2017—previously known only from northern India, northern Myanmar and Indochina, respectively, are reported from Nepal for the first time. Plateros anguliplanatus Kazantsev, 2021, syn. nov. is synonymised with P. gurkha Kazantsev, 2001. Fourteen species of Plateros from Nepal—P. atrosuturalis Kazantsev, 2011, P. brancuccii Kazantsev, 1991, P. cimicoides Kleine, 1928, P. cinereus Kazantsev, 1991, P. dentifer Kazantsev, 1991, P. harmandi Bourgeois, 1928, P. karnaliensis Kazantsev, 2011, P. kumatai Nakane, 1983, P. laterculus Kazantsev, 1991, P. macrosuturalis Kazantsev, 1991, P. manaliensis (Bocáková, 1997), P. nepalensis Kazantsev, 1991, P. suturalis Pic, 1928, and P. wittmerianus Kazantsev, 1991—are illustrated with colour photographs of their habitus and aedeagi for the first time. A comprehensive list of Plateros species in Nepal is presented, now encompassing a total of 36 species.
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Chlorophorus Chevrolat, 1863, one of the most species-rich genera of Clytini, comprises 36 subgenera and 302 species/subspecies, with some species being of significant economic importance. To assess the monophyly and subgeneric system of this genus, we newly obtained mitochondrial genomic data from 21 species of Chlorophorus via high-throughput sequencing and reconstructed the phylogeny of this genus using ML and BI methods. The mitochondrial genomes of all sequenced Chlorophorus species were found to comprise 13 protein-coding genes (PCGs), 22 transfer RNAs (tRNAs), two ribosomal RNAs (rRNAs), and one non-coding region (control region, CR), reflecting a highly conserved gene arrangement. The mitochondrial genomes of the 21 Chlorophorus species range from 15,387 bp to 15,779 bp in length, and all exhibited AT bias. Analysis of the non-synonymous and synonymous substitution rates revealed that ATP8 has the highest evolution rate, whereas COI has the lowest. Further, phylogenetic analyses were performed based on different datasets (13 PCGs + 2 rRNAs, 13 PCGs + 2 rRNAs + 22 tRNAs, PCG123, PCG12) using maximum likelihood (ML) and Bayesian inference (BI) methods. The results indicate that Chlorophorus is monophyletic, but the subgenera Humeromaculatus Özdikmen, 2011; Immaculatoides Özdikmen, 2022; Brevenotatus Özdikmen, 2022; and Chlorophorus (s. str.) Chevrolat, 1863, are not monophyletic. Based on the comparison of male genitalia, we found that the sclerites of the endophallus may exhibit phylogenetic signals for the genus.
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Chlorophorus fainanensis Pic, 1918 is redescribed. Four species, C. coniperda Holzschuh, 1992, C. diversicolor Holzschuh, 2016, C. orbatus Holzschuh, 1991 and C. pinguis Holzschuh, 1992 are newly reported from China. A new synonymy, Chlorophorus arciferus (Chevrolat, 1863) = Chlorophorus semisinuatus Pic, 1949, syn. nov. is proposed.
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A contribution to the knowledge of the malachiine genus Intybia Pascoe, 1866 from China is given. Two new species groups: Intybia klapperichi group and Intybia eversi group are defined and described. A new species, Intybia hainanensis Wang & Liu, sp. nov., of the Intybia klapperichi group is described from Hainan Province. Intybia erectodentatus (Wittmer, 1982) and Intybia concha Asano, 2015 are redescribed based on new materials collected in mainland China. A key to species groups of the genus Intybia Pascoe, 1866 in China is provided.
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A new species group of Lilioceris Reitter, 1913 is proposed and reviewed, the semipunctata group. It includes eleven species: L. atrilateralis Kimoto & Takizawa, 1973, L. consentanea (Lacordaire, 1845), L. dentifemoralis Long, 1988, L. discrepens (Baly, 1879), L. jianfenglingensis Long, 1988, L. latissima (Pic, 1932), L. lianzhouensis Long, 2000a, L. rondoni Kimoto & Gressitt, 1979, L. rufometallica (Pic, 1923), L. semipunctata (Fabricius, 1801), and L. yuae Long, 2000b. Lilioceris discrepens and L. rondoni were new records from China. Two synonyms are proposed: Lilioceris xinglongensis Long, 1988, syn. nov. of L. consentanea (Lacordaire, 1845), and Crioceris rufimembris Pic, 1921, syn. nov. of L. semipunctata . An identification key, descriptions, habitus photographs, geographic distributions, host plants and habitats (if available), are provided for these species.
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The genus Pseudocerocoma Pic, 1919 (Coleoptera: Cantharidae: Ichthyurini) was previously recognized as a monotypic genus. Based on material from Antioquia, Colombia, we describe and illustrate Pseudocerocoma tulenapa sp. nov. It differs from the other known species of the genus in the shape of the antennae and the abdominal segment 8, as well as in some aspects of coloration. This new species provides additional evidence for the position of Pseudocerocoma Pic, 1919 as a separate genus from Malthoichthyurus Pic, 1919, also represents the first record of the tribe Ichthyurini in Colombia and shows the importance of the conservation actions carried out in the only known locality, the Tulenapa Biological Station of the Universidad de Antioquia.
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The tribes Goniaderini Lacordaire, 1859 and Lupropini Lesne, 1926 within the tenebrionid subfamily Lagriinae Latreille, 1825 have previously been shown to be non-monophyletic by molecular phylogenetic analyses. The tribes and constituent genera are here reviewed and redefined morphologically. As part of tribal redefinitions, we establish Prateini New Tribe with type genus Prateus LeConte, 1862. We reestablish the subtribe Phobeliina Ardoin, 1961 Revised Status , which is transferred from Goniaderini and placed as a subtribe of Lagriini Latreille, 1825 where it is comprised of Phobelius Blanchard, 1842, and Rhosaces Champion, 1889 (previously in Lagriini: Statirina Blanchard, 1845). The fossil tribe Archaeolupropini Nabozhenko, Perkovsky, & Nazarenko, 2023 is transferred from Lagriinae to Tetratomidae: Tetratominae Billberg, 1820. Keys to extant tribes and subtribes of Lagriinae and genera of Goniaderini, Lupropini, and Prateini are provided. Generic and species-level changes from this work are as follows: Prateini is comprised of the following 15 genera: Antennoluprops Schawaller, 2007, Ardoiniellus Schawaller, 2013, Bolitrium Gebien, 1914, Enicmosoma Gebien, 1922, Indenicmosoma Ardoin, 1964, Iscanus Fauvel, 1904, Kuschelus Kaszab, 1982, Lorelopsis Champion, 1896, Mesotretis Bates, 1872, Microcalcar Pic, 1925, Micropedinus Lewis, 1894, Paratenetus Spinola, 1845, Prateus , Terametus Motschulsky, 1869, and Tithassa Pascoe, 1860. Lorelus Sharp, 1876 is Returned to Synonymy with Prateus , resulting in the following 49 New Combinations : Prateus angulatus (Doyen & Poinar, 1994), P. angustulus (Champion, 1913), P. armatus (Montrouzier, 1860), P. biroi (Kaszab, 1956), P. blairi (Kaszab, 1955), P. brevicornis (Champion, 1896), P. breviusculus (Champion, 1913), P. caledonicus (Kaszab, 1982), P. carolinensis (Blair, 1940), P. chinensis (Kaszab, 1940), P. clarkei (Kulzer, 1957), P. crassicornis (Broun, 1880), P. crassepunctatus (Kaszab, 1982), P. cribricollis (Kaszab, 1940), P. curvipes (Champion, 1913), P. dybasi (Kulzer, 1957), P. fijianus (Kaszab, 1982), P. fumatus (Lea, 1929), P. glabriventris (Kaszab, 1982), P. greensladei (Kaszab, 1982), P. guadeloupensis (Kaszab, 1940), P. hirtus (Kaszab, 1982), P. ivoirensis (Ardoin, 1969), P. kanak (Kaszab, 1986), P. kaszabi (Watt, 1992), P. laticornis (Watt, 1992), P. latulus (Broun, 1910), P. longicornis (Kaszab, 1982), P. mareensis (Kaszab, 1982), P. marginalis (Broun, 1910), P. niger (Kaszab, 1982), P. norfolkianus (Kaszab, 1982), P. obtusus (Watt, 1992), P. ocularis (Fauvel, 1904), P. opacus (Watt, 1992), P. palauensis (Kulzer, 1957), P. politus (Watt, 1992), P. priscus (Sharp, 1876), P. prosternalis (Kaszab, 1982), P. pubescens (Broun, 1880), P. pubipennis (Lea, 1929), P. punctatus (Watt, 1992), P. quadricollis (Broun, 1886), P. queenslandicus (Kaszab, 1986), P. rugifrons (Champion, 1913), P. solomonis (Kaszab, 1982), P. tarsalis (Broun, 1910), P. unicornis (Kaszab, 1982), and P. watti (Kaszab, 1982). Microlyprops Kaszab, 1939 is placed as a New Synonym of Micropedinus resulting in the following New Combinations : Micropedinus ceylonicus (Kaszab, 1939) and M. maderi (Kaszab, 1940). Lorelopsis Revised Status is revalidated as a genus and eight species formerly in Lorelus are transferred to it resulting in the following six New Combinations : Lorelopsis bicolor (Doyen, 1993), L. glabrata (Doyen, 1993), L. exilis (Champion, 1913), L. foraminosa (Doyen & Poinar, 1994), L. minutulis (Doyen & Poinar, 1994), L. trapezidera (Champion, 1913), and L. wolcotti (Doyen, 1993). Lorelopsis pilosa Champion, 1896 becomes a Restored Combination . In Goniaderini, Aemymone Bates, 1868 Revised Status and Opatresthes Gebien, 1928 Revised Status , which were recently considered as subgenera of Goniadera Perty, 1832, are restored as valid genera based on new character analysis resulting in the following New Combinations : Aemymone hansfranzi (Ferrer & Delatour, 2007), A. simplex (Fairmaire, 1889), A. striatipennis (Pic, 1934) and Restored Combinations : Aemymone cariosa (Bates, 1868), A. crenata Champion, 1893, and A. semirufa Pic, 1917. Gamaxus Bates, 1868 is Returned to Synonymy with Phymatestes Pascoe, 1866, and the type species Gamaxus hauxwelli Bates, 1868 is placed as a New Synonym of Phymatestes brevicornis (Lacordaire, 1859). The following seven genera are placed as New Synonyms of Anaedus Blanchard, 1842: Microanaedus Pic, 1923, Pengaleganus Pic, 1917, Pseudanaedus Gebien, 1921, Pseudolyprops Fairmaire, 1882, Spinolyprops Pic, 1917, Spinadaenus Pic, 1921, and Sphingocorse Gebien, 1921. Fourteen species described by Pic in Aspisoma Duponchel & Chevrolat, 1841 (not Aspisoma Laporte, 1833) are returned to Tenebrionidae as valid species of Anaedus . These synonymies necessitate the following 51 New Combinations : Anaedus albipes (Gebien, 1921), A. amboinensis (Kaszab, 1964), A. amplicollis (Fairmaire, 1896), A. anaedoides (Gebien, 1921), A. angulicollis (Gebien, 1921), A. angustatus (Pic, 1921), A. australiae (Carter, 1930), A. bartolozzii (Ferrer, 2002), A. beloni Fairmaire, 1888), A. biangulatus (Gebien, 1921), A. borneensis (Pic, 1917), A. carinicollis (Gebien, 1921), A. conradti (Gebien, 1921), A. cribricollis (Schawaller, 2012), A. gabonicus (Pic, 1917), A. himalayicus (Kaszab, 1965), A. inaequalis (Pic, 1917), A. jacobsoni (Gebien, 1927), A. lateralis (Pic, 1917), A. latus (Pic, 1917), A. longeplicatus (Gebien, 1921) , A. maculipennis (Schawaller, 2011), A. major (Pic, 1917), A. nepalicus (Kaszab, 1975), A. nigrita (Gebien, 1927), A. notatus (Pic, 1923), A. pakistanicus (Schawaller, 1996), A. pinguis (Gebien, 1927), A. punctatus (Carter, 1914), A. raffrayi (Pic, 1917), A. rufithorax (Pic, 1917), A. rufus (Pic, 1917), A. serrimargo (Gebien, 1914), A. sumatrensis (Pic, 1917), A. terminatus (Gebien, 1921), A. testaceicornis (Pic, 1921), A. testaceipes (Pic, 1917), A. thailandicus (Schawaller, 2012), A. trautneri (Schawaller, 1994); and 13 restored combinations: Anaedus boliviensis (Pic, 1934), A. claveri (Pic, 1917), A. diversicollis (Pic, 1917), A. elongatus (Pic, 1934), A. guyanensis (Pic, 1917), A. holtzi (Pic, 1934), A. inangulatus (Pic, 1934), A. inhumeralis (Pic, 1917), A. mendesensis (Pic, 1917), A. minutus (Pic, 1917), A. rufimembris (Pic, 1932), A. rufipennis (Pic, 1917), A. subelongatus (Pic, 1932). The new synonymies with Anaedus necessitate the following six New Replacement Names Anaedus maculipennis (for Spinolyprops maculatus Kulzer, 1954), A. grimmi (for Aspisoma forticornis Pic, 1917), A. minimus (for Anaedus minutus Pic, 1938), A. merkli (for Anaedus diversicollis Pic, 1938), A. ottomerkli (for Anaedus lateralis Pic, 1923), A. schawalleri (for Anaedus nepalicus Schawaller, 1994). Capeluprops Schawaller, 2011 is removed from Lupropini and provisionally placed in Laenini Seidlitz, 1895. Plastica Waterhouse, 1903 is transferred from Apocryphini Lacordaire, 1859 to Laenini. Paralorelopsis Marcuzzi, 1994 is removed from Lupropini and provisionally placed in Lagriinae incertae sedis. Pseudesarcus Champion, 1913 is transferred from Lagriinae incertae sedis to Diaperinae incertae sedis. Falsotithassa Pic, 1934 is transferred from Lupropini to Leiochrinini Lewis, 1894 (Diaperinae). Mimocellus Wasmann, 1904 is transferred from Lupropini to Tenebrionidae incertae sedis, and likely belongs in either Diaperinae or Stenochiinae.
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Osphya Illiger (Melandryidae: Osphyinae) as a species-poor insect group, exhibits a widespread distribution in the Northern Hemisphere, however, the research of the genus is poorly documented especially in East Asia. Herein, an interesting species is discovered in Shennongjia National Natural Reserve (Hubei, China). The examination of morphological characters and comparisons with others show it to be a new member of Osphya, which is described under the name of O. sinensis sp. n. The characteristic photos and a key to the species of Osphya from East Asia are provided. Meanwhile, the mitochondrial genome of O. sinensis sp. n. is sequenced and annotated. Based on this obtained mitogenome and the publicly available data, we reconstructed the phylogeny of Tenebrionoidea by different cladistics methods to investigate the relationships between the new species with others. The results consistently recover O. sinensis sp. n. sister to O. bipunctata (Fabricius) with high supporting values, which further confirm the placement of the new species in the genus Osphya. This is the first time reporting the genus Osphya, the only representative genus of melandryid Osphyinae from mainland China, which enriches the diversity of beetles from the Chinese fauna at both generic and subfamilial levels.
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A review of genus-group names for darkling beetles in the family Tenebrionidae (Insecta: Coleoptera) is presented. A catalogue of 4122 nomenclaturally available genus-group names, representing 2307 valid genera (33 of which are extinct) and 761 valid subgenera, is given. For each name the author, date, page number, gender, type species, type fixation, current status, and first synonymy (when the name is a synonym) are provided. Genus-group names in this family are also recorded in a classification framework, along with data on the distribution of valid genera and subgenera within major biogeographical realms. A list of 535 unavailable genus-group names (e.g., incorrect subsequent spellings) is included. Notes on the date of publication of references cited herein are given, when known. The following genera and subgenera are made available for the first time: Anemiadena Bouchard & Bousquet, subgen. nov. (in Cheirodes Gené, 1839), Armigena Bouchard & Bousquet, subgen. nov. (in Nesogena Mäklin, 1863), Debeauxiella Bouchard & Bousquet, subgen. nov. (in Hyperops Eschscholtz, 1831), Hyperopsis Bouchard & Bousquet, subgen. nov. (in Hyperops Eschscholtz, 1831), Linio Bouchard & Bousquet, subgen. nov. (in Nilio Latreille, 1802), Matthewsotys Bouchard & Bousquet, gen. nov. , Neosolenopistoma Bouchard & Bousquet, subgen. nov. (in Eurynotus W. Kirby, 1819), Paragena Bouchard & Bousquet, subgen. nov. (in Nesogena Mäklin, 1863), Paulianaria Bouchard & Bousquet, gen. nov. , Phyllechus Bouchard & Bousquet, gen. nov. , Prorhytinota Bouchard & Bousquet, subgen. nov. (in Rhytinota Eschscholtz, 1831), Pseudorozonia Bouchard & Bousquet, subgen. nov. (in Rozonia Fairmaire, 1888), Pseudothinobatis Bouchard & Bousquet, gen. nov. , Rhytinopsis Bouchard & Bousquet, subgen. nov. (in Thalpophilodes Strand, 1942), Rhytistena Bouchard & Bousquet, subgen. nov. (in Rhytinota Eschscholtz, 1831), Spinosdara Bouchard & Bousquet, subgen. nov. (in Osdara Walker, 1858), Spongesmia Bouchard & Bousquet, subgen. nov. (in Adesmia Fischer, 1822), and Zambesmia Bouchard & Bousquet, subgen. nov. (in Adesmia Fischer, 1822). The names Adeps Gistel, 1857 and Adepsion Strand, 1917 syn. nov. [= Tetraphyllus Laporte & Brullé, 1831], Asyrmatus Canzoneri, 1959 syn. nov. [= Pystelops Gozis, 1910], Euzadenos Koch, 1956 syn. nov. [= Selenepistoma Dejean, 1834], Gondwanodilamus Kaszab, 1969 syn. nov. [= Conibius J.L. LeConte, 1851], Gyrinodes Fauvel, 1897 syn. nov. [= Nesotes Allard, 1876], Helopondrus Reitter, 1922 syn. nov. [= Horistelops Gozis, 1910], Hybonotus Dejean, 1834 syn. nov. [= Damatris Laporte, 1840], Iphthimera Reitter, 1916 syn. nov. [= Metriopus Solier, 1835], Lagriomima Pic, 1950 syn. nov. [= Neogria Borchmann, 1911], Orphelops Gozis, 1910 syn. nov. [= Nalassus Mulsant, 1854], Phymatium Billberg, 1820 syn. nov. [= Cryptochile Latreille, 1828], Prosoblapsia Skopin & Kaszab, 1978 syn. nov. [= Genoblaps Bauer, 1921], and Pseudopimelia Gebler, 1859 syn. nov. [= Lasiostola Dejean, 1834] are established as new synonyms (valid names in square brackets). Anachayus Bouchard & Bousquet, nom. nov. is proposed as a replacement name for Chatanayus Ardoin, 1957, Genateropa Bouchard & Bousquet, nom. nov. as a replacement name for Apterogena Ardoin, 1962, Hemipristula Bouchard & Bousquet, nom. nov. as a replacement name for Hemipristis Kolbe, 1903, Kochotella Bouchard & Bousquet, nom. nov. as a replacement name for Millotella Koch, 1962, Medvedevoblaps Bouchard & Bousquet, nom. nov. as a replacement name for Protoblaps G.S. Medvedev, 1998, and Subpterocoma Bouchard & Bousquet, nom. nov. is proposed as a replacement name for Pseudopimelia Motschulsky, 1860. Neoeutrapela Bousquet & Bouchard, 2013 is downgraded to a subgenus ( stat. nov. ) of Impressosora Pic, 1952. Anchomma J.L. LeConte, 1858 is placed in Stenosini: Dichillina (previously in Pimeliinae: Anepsiini); Entypodera Gerstaecker, 1871, Impressosora Pic, 1952 and Xanthalia Fairmaire, 1894 are placed in Lagriinae: Lagriini: Statirina (previously in Lagriinae: Lagriini: Lagriina); Loxostethus Triplehorn, 1962 is placed in Diaperinae: Diaperini: Diaperina (previously in Diaperinae: Diaperini: Adelinina); Periphanodes Gebien, 1943 is placed in Stenochiinae: Cnodalonini (previously in Tenebrioninae: Helopini); Zadenos Laporte, 1840 is downgraded to a subgenus ( stat. nov. ) of the older name Selenepistoma Dejean, 1834. The type species [placed in square brackets] of the following available genus-group names are designated for the first time: Allostrongylium Kolbe, 1896 [ Allostrongylium silvestre Kolbe, 1896], Auristira Borchmann, 1916 [ Auristira octocostata Borchmann, 1916], Blapidocampsia Pic, 1919 [ Campsia pallidipes Pic, 1918], Cerostena Solier, 1836 [ Cerostena deplanata Solier, 1836], Coracostira Fairmaire, 1899 [ Coracostira armipes Fairmaire, 1899], Dischidus Kolbe, 1886 [ Helops sinuatus Fabricius, 1801], Eccoptostoma Gebien, 1913 [ Taraxides ruficrus Fairmaire, 1894], Ellaemus Pascoe, 1866 [ Emcephalus submaculatus Brême, 1842], Epeurycaulus Kolbe, 1902 [ Epeurycaulus aldabricus Kolbe, 1902], Euschatia Solier, 1851 [ Euschatia proxima Solier, 1851], Heliocaes Bedel, 1906 [ Blaps emarginata Fabricius, 1792], Hemipristis Kolbe, 1903 [ Hemipristis ukamia Kolbe, 1903], Iphthimera Reitter, 1916 [ Stenocara ruficornis Solier, 1835], Isopedus Stein, 1877 [ Helops tenebrioides Germar, 1813], Malacova Fairmaire, 1898 [ Malacova bicolor Fairmaire, 1898], Modicodisema Pic, 1917 [ Disema subopaca Pic, 1912], Peltadesmia Kuntzen, 1916 [ Metriopus platynotus Gerstaecker, 1854], Phymatium Billberg, 1820 [ Pimelia maculata Fabricius, 1781], Podoces Péringuey, 1886 [ Podoces granosula Péringuey, 1886], Pseuduroplatopsis Pic, 1913 [ Borchmannia javana Pic, 1913], Pteraulus Solier, 1848 [ Pteraulus sulcatipennis Solier, 1848], Sciaca Solier, 1835 [ Hylithus disctinctus Solier, 1835], Sterces Champion, 1891 [ Sterces violaceipennis Champion, 1891] and Teremenes Carter, 1914 [ Tenebrio longipennis Hope, 1843]. Evidence suggests that some type species were misidentified. In these instances, information on the misidentification is provided and, in the following cases, the taxonomic species actually involved is fixed as the type species [placed in square brackets] following requirements in Article 70.3 of the International Code of Zoological Nomenclature: Accanthopus Dejean, 1821 [ Tenebrio velikensis Piller & Mitterpacher, 1783], Becvaramarygmus Masumoto, 1999 [ Dietysus nodicornis Gravely, 1915], Heterophaga Dejean, 1834 [ Opatrum laevigatum Fabricius, 1781], Laena Dejean, 1821, [ Scaurus viennensis Sturm, 1807], Margus Dejean, 1834 [ Colydium castaneum Herbst, 1797], Pachycera Eschscholtz, 1831 [ Tenebrio buprestoides Fabricius, 1781], Saragus Erichson, 1842 [ Celibe costata Solier, 1848], Stene Stephens, 1829 [ Colydium castaneum Herbst, 1797], Stenosis Herbst, 1799 [ Tagenia intermedia Solier, 1838] and Tentyriopsis Gebien, 1928 [ Tentyriopsis pertyi Gebien, 1940]. The following First Reviser actions are proposed to fix the precedence of names or nomenclatural acts (rejected name or act in square brackets): Stenosis ciliaris Gebien, 1920 as the type species for Afronosis G.S. Medvedev, 1995 [ Stenosis leontjevi G.S. Medvedev, 1995], Alienoplonyx Bremer, 2019 [ Alienolonyx ], Amblypteraca Mas-Peinado, Buckley, Ruiz & García-París, 2018 [ Amplypteraca ], Caenocrypticoides Kaszab, 1969 [ Caenocripticoides ], Deriles Motschulsky, 1872 [ Derilis ], Eccoptostira Borchmann, 1936 [ Ecoptostira ], † Eodromus Haupt, 1950 [† Edromus ], Eutelus Solier, 1843 [ Lutelus ], Euthriptera Reitter, 1893 [ Enthriptera ], Meglyphus Motschulsky, 1872 [ Megliphus ], Microtelopsis Koch, 1940 [ Extetranosis Koch, 1940, Hypermicrotelopsis Koch, 1940], Neandrosus Pic, 1921 [ Neoandrosus ], Nodosogylium Pic, 1951 [ Nodosogilium ], Notiolesthus Motschulsky, 1872 [ Notiolosthus ], Pseudeucyrtus Pic, 1916 [ Pseudocyrtus ], Pseudotrichoplatyscelis Kaszab, 1960 [ Pseudotrichoplatynoscelis and Pseudotrichoplatycelis ], Rhydimorpha Koch, 1943 [ Rhytimorpha ], Rhophobas Motschulsky, 1872 [ Rophobas ], Rhyssochiton Gray, 1831 [ Ryssocheton and Ryssochiton ], Sphaerotidius Kaszab, 1941 [ Spaerotidius ], Stira Agassiz, 1846 (Mollusca) [ Stira Agassiz, 1846 (Coleoptera)], Sulpiusoma Ferrer, 2006 [ Sulpiosoma ] and Taenobates Motschulsky, 1872 [ Taeniobates ]. 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