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Based on molecular and morphological data of four specimens of Pareas Wagler, 1830 collected from the type locality of P. yunnanensis (Vogt, 1922), along with examination of the type specimens of P. yunnanensis, we revalidate this poorly known, secretive species. Furthermore, based on molecular and morphological lines of evidence we also describe a new species of Pareas from Xishuangbanna Prefecture, Yunnan Province, China. Morphologically, the new species closely resembles its sister species P. nigriceps Guo & Deng, 2009. However, the new species is divergent from the latter in cytochrome b mtDNA gene sequences, and can be distinguished from all congeners by the following combination of morphological characteristics: single preocular, postocular fused with subocular, loreal not bordering orbit, vertebral scales enlarged, 3–5 rows of mid-dorsal scales keeled at the middle of the body, ventral scales 160–171; subcaudals 62–64, dorsal surface of head solid black or reddish-brown, dark nuchal band present, iris brownish-black or reddish-brown.
New distribution and host records plus additional notes are provided for North American species in the genus Chrysobothris Eschscholtz (Coleoptera: Buprestidae). Forty-one species are treated. The occurrence of Chrysobothris bicolor Horn in the USA is refuted. Chrysobothris breviloboides Barr is newly synonymized with Chrysobothris breviloba Fall. The southernmost record for Chrysobothris piuta Wickham, from Baja California, Mexico, is established. A specimen of the Argentinian Chrysobothris rugosa Gory and Laporte labeled from Florida is reported. A lectotype for Chrysobothris vulcanica LeConte is newly designated.
ZooBank registration. urn:lsid:zoobank.org:pub:FDB5C4A4-548C-4436-92BB-59AE3183378C
Juga is a genus of freshwater snails distributed from northern Washington to central California. The taxonomy and classification of the genus has a long and complex history, driven mainly by the features of their highly variable shells. The number of recognized species has fluctuated from ~9 to 11; however, it has been claimed that the actual diversity may be three times that number. We here present a systematic revision using a recently published molecular phylogeny as a framework, which supported the interpretation that there are only nine valid species. Comprehensive review of type material and original descriptions for all available species-group names indicates that almost all species previously considered valid were para- or polyphyletic grades of organization in shell morphology. Most species previously suggested to be putatively new were confirmed to be morphological variants of species already described. Species accounts include complete synonymies and partial chresonymies; the shells and radulae are illustrated and described. Lectotypes are designated for Melania plicifera Lea, 1838, M. silicula Gould, 1847, and M. rudens Reeve, 1860. Three species, Juga caerulea sp. nov., J. canella sp. nov., and J. douglasi sp. nov., are described as new and one species is excluded from the genus. The subgenera Calibasis D.W. Taylor, 1966 and Idabasis D.W. Taylor, 1966 are synonymized with Juga.
A taxonomic review of tenebrionid platyopoid genera of the subfamily Pimeliinae from Eastern Europe, Central Asia, Afghanistan, Iran and Pakistan is given. This group of taxa was known before 1994 as the tribe Platyopini Motschulsky, 1849, which is now interpreted as a junior synonym of Pimeliini Latreille, 1802. The group is different from other Pimeliini in having dorso-lateral eyes, located above the level of the genae, and it includes the following ultrapsammophilic genera at least from Central and Southern Asia: Apatopsis Semenov, 1891, Habrochiton Semenov-Tjan-Shansky, 1907, Habrobates Semenov, 1903 [= Kawiria Schuster, 1935 syn. nov.], Dietomorpha Reymond, 1938, Przewalskia Semenov, 1893, Mantichorula Reitter, 1889, Platyope Fischer von Waldheim, 1820 [= Homopsis Semenov, 1893 syn. nov.], Earophanta Semenov, 1903. These genera are distributed in almost all large deserts of Palaearctic Asia: Karakum, Kyzylkum, Muyunkum, Taklamakan, Gobi, Registan, Dasht-e-Kawir, Dasht-e-Lut, as well as in other arid and semi-arid sandy landscapes from European Russia to the south of Eastern Siberia. The group of platyopoid genera is polyphyletic. We propose at least two monophyletic branches: the Habrobates genus group (the first four genera mentioned above), which represents the subtribe Habrobatina Nabozhenko & S. Chigray subtrib. nov. and the Platyope genus group (latter four genera) within the nominotypical subtribe. A new species is described from Pakistan (Balochistan): Dietomorpha gonzalesi S. Chigray & Nabozhenko sp. nov. Platyope granulata Fischer von Waldheim, 1820 is recorded for Kazakhstan for the first time. The following synonymy is resurrected: Apatopsis grombczewskii Semenov, 1890 = Apatopsis conradti Semenov, 1890, syn. resurr. Two new combinations resulting from the synonymy of genera are given: Habrobates gabrieli Schuster, 1935 comb. nov. (from Kawiria), Platyope grumi Semenov, 1893 comb. nov. (from Homopsis). Lectotypes are designated for the following taxa: Apatopsis grombczewskii (Semenov, 1891), Apatopsis conradti Semenov, 1891, Habrochiton vernus Semenov-Tjan-Shansky, 1907, Habrobates vernalis Semenov, 1903, Kawiria gabrieli Schuster, 1935, Platyope dilatata Reitter, 1887; Mantichorula semenowi Reitter, 1889, Mantichorula grandis Semenov, 1893, Homopsis grumi Semenov, 1893, Platyope serrata Semenov, 1893, Platyope planidorsis Reitter, 1889, Platyope tomentosa Semenov, 1893. Additional information for type specimens studied by the authors is given for Habrochiton primaeveris Semenov-Tjan-Shansky, 1907 (holotype), Habrobates vejisovi Kelejnikova, 1977, Platyope ordossica Semenov-Tjan-Shansky, 1907 (holotype), Earophanta autumnalis Semenov, 1903 (holotype, junior synonym of E. planidorsis Reitter, 1889), Earophanta loudoni Semenov, 1903 (holotype, junior synonym of Earophanta pilosissima Reitter, 1895), Earophanta pubescens Skopin, 1960 (holotype, paratypes), Earophanta beludzhistana Bogatchev, 1957 (holotype).
The following new species of Eupogonius LeConte, 1852 (Coleoptera: Cerambycidae: Lamiinae) are described: E. tlanchinolensis Wappes and Santos-Silva (Mexico, Hidalgo); E. albofasciatus Wappes and Santos- Silva (Mexico, Puebla); E. sonorensis Wappes and Santos-Silva (Mexico, Sonora); E. guerrerensis Wappes and Santos-Silva (Mexico, Guerrero); E. boteroi Wappes and Santos-Silva (Mexico, Guerrero); E. nascimentoi Wappes and Santo-Silva (Mexico, Jalisco and Colima); and E. monzoni Wappes and Santos-Silva (Guatemala, Alta Verapaz). Additionally, a detailed description of the female of Eupogonius fulvovestitus Schaeffer, 1905 is provided for the first time, along with notes on the likely host of the species. New state records in Mexico are provided for Eupogonius comus Bates, 1885, and E. stellatus Chemsak and Noguera, 1995. Other taxonomic or nomenclatural actions included herein are: Eupogonius knabi Fisher, 1925 is transferred to Atelodesmis Chevrolat, 1841, new combination; the gender of the species-group name in Eupogonius azteca Martins, Santos-Silva and Galileo, 2015 is commented on; notes on the geographical distribution of Eupogonius affinis Breuning, 1942, and the problematic morphology of E. infimus (Thomson, 1868) are presented; Eupogonius subaeneus Bates, 1872, and E. marmoratus Fisher, 1925 are revalidated, and E. columbianus Breuning, 1942 is a new synonym of E. subaeneus”.
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.
New species and taxonomical notes in Gorybia Pascoe, 1866 (Coleoptera: Cerambycidae: Cerambycinae)
(2019)
Three new Gorybia Pascoe, 1866 (Coleoptera: Cerambycidae: Cerambycinae: Piezocerini), species from Bolivia are described: G. martinsi Wappes, Botero and Santos-Silva new species; G. galileoae Wappes, Botero and Santos-Silva, new species; and G. clarkeorum Wappes, Botero and Santos-Silva, new species. In addition, G. bispinosa Martins, Galileo and Limeira-de-Oliveira, 2009 is proposed as a synonym of G. castanea (Gounelle, 1909) and G. maculosa Martins, 1976 as a synonym of G. apatheia Martins, 1976.
Morphological and cytochrome oxidase 1 (Cox1) data show that Aphis floridanae Tissot (Hemiptera: Aphididae) is not synonymous with A. nasturtii Kaltenbach. Instead, A. floridanae matches the morphological characters of A. impatientis Thomas. Additionally, the range of cytochrome oxidase 1 (Cox1) pair-wise distance of the multiple collections of A. impatientis on Cornus spp., Impatiens spp. and Erechtites hieraciifolius (L.) Raf. ex DC. is 0–0.39%. Therefore, we conclude that A. floridanae Tissot, 1933 is a junior synonym of A. impatientis Thomas, 1878, new synonymy. In addition, A. impatientis is re-described, including first descriptions of the ovipara and alate male of that species.
The present study redescribes four species of Neanthes Kinberg, 1865 (Nereididae de Blainville, 1818) based on their type specimens collected from different worldwide localities: Neanthes chilkaensis (Southern, 1921) from India, N. galetae (Fauchald, 1977) from Panama, N. helenae (Kinberg, 1865) from St Helena Island, and N. mossambica (Day, 1957) from Mozambique. The morphology of the types was re-examined for the first time after the species were originally described, and incorporated the recent improvements in the standards and terminology for describing nereidid features. The arrangement of paragnaths on area VI stood out among the diagnostic features used to distinguish these four species. Neanthes chilkaensis and N. helenae are the unique nereidids bearing p-bar paragnaths on the area VI. Both species are also distinctive as the former species only exhibited p-bar paragnaths on the area VII–VIII and the latter ventrolateral projections on the apodous segment. Further examination revealed that N. nanciae (Day, 1949) from St Helena is a junior synonym of N. helenae. Moreover, N. galetae and N. mossambica are distinguishable from other species also by the development of dorsal cirri, neuropodial postchaetal lobe and ventral ligule, the presence/absence of merged paragnaths on area IV, paired oesophageal caeca, among other features. This study has further contributed to the morphological delimitation of the species in Neanthes as a first step towards revising the genus.