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Within the central European opilionid fauna the widely used species names Leiobunum rupestre Herbst, 1799 and Leiobunum tisciae Avram, 1968 pose taxonomic and distributional problems. In addition, Nelima apenninica Martens, 1969 is close to L. tisciae in terms of external and genital morphology, but is specifically distinct. While coxal denticulation is largely lacking in N. apenninica, the validity of the genus Nelima Roewer, 1910 is questioned again. In addition, Leiobunum subalpinum Komposch, 1998, a recently described novelty from the eastern Alps, is closely related to L. rupestre. The four species are combined as the morphologically defined Leiobunum rupestre species group. Except for L. subalpinum, they were found to be allopatrically distributed from the Carpathians across central and Northwest Europe to the south-western Alps. The latter species is locally sympatric and partly elevationally parapatric to L. rupestre. Leiobunum tisciae is a recently introduced name and here recognized as a junior synonym of a number of taxa described much earlier, of which L. gracile Thorell, 1876 is re-introduced as oldest available name. Detailed morphological and distributional data for all taxa are presented.
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.
Arising from a number of 2019 IUCN Red List assessments for a subset of Chinese Odonata, a series of corrections and taxonomic revisions were made to the World Odonata List. The rationale for these amendments is provided here. Paragomphus wuzhishanensis Liu, 1988 is shown to be a junior synonym of Paragomphus pardalinus Needham (1942). Epophthalmia kuani Jiang 1998 is synonymised as a junior synonym of Epophthalmia. elegans (Brauer, 1865) and Epophthalmia bannaensis Zha & Jiang, 2010 is treated as a junior synonym of Epophthalmia vittata Burmeister, 1839. Idionyx pseudovictor Xu, 2013 is shown to be junior synonym of Idionyx claudia Ris, 1912 and Sympetrum anomalum Needham, 1930 is treated as a junior synonym of Sympetrum maculatum Oguma, 1922.
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.
We revise the genus Attemsostreptus Verhoeff, 1941 based on type material of the type species, A. costatus Verhoeff, 1941, synonymise A. orobius (Kraus 1958) with A. costatus and describe a second species of the genus, A. reflexus sp. nov., collected from Kimboza Forest Reserve in Tanzania, and discuss the dubious tribe Trachystreptini.
A revision was done on the species of Enteromius Cope, 1867 (Cypriniformes: Cyprinidae) from the Lake Edward system with a smooth, flexible third unbranched dorsal fin ray without serrations. Specimens with these characteristics had previously been attributed to E. perince and E. stigmatopygus. A combination of a genetic (COI, mtDNA) and a morphometric approach was used. Based on the COI gene, we found two groups with a distance of 8.5%, though neither of the two corresponded to E. perince or E. stigmatopygus. One group revealed to be conspecific with E. alberti, previously a synonym of E. stigmatopygus, described from the Rutshuru River, May-Ya-Moto (DRC, Lake Edward system), and revalidated here. In addition, E. cercops, described from the Nzoia River (Kenya, Lake Victoria basin), is put in synonymy with E. alberti. The second group was most similar to E. mimus, but differed morphologically somewhat from the types of E. mimus. Therefore, specimens of this group were identified as E. cf. mimus. Morphologically, E. alberti can be separated from E. cf. mimus based on a higher number of lateral line scales and smaller values for interorbital width, pre-pelvic distance, body depth, maximum and minimum caudal peduncle depth, head width and head depth.
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.
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.
This paper presents an improved diagnosis and definition of the genus Stenaelurillus Simon, 1886, with new taxonomic and faunistic data for 23 species. The genera Microheros Wesołowska & Cumming, 1999 and Mashonarus Wesołowska & Cumming, 2002 are synonymized with Stenaelurillus. Six new species are described: Stenaelurillus bandama sp. nov. (♂♀, from Côte d’Ivoire), S. belihuloya sp. nov. (♂, from Sri Lanka), S. jocquei sp. nov. (♂♀, from Cameroon), S. pseudoguttatus sp. nov. (♂, from Namibia), S. senegalensis sp. nov. (♂♀, from Senegal), and Stenaelurillus siyamae sp. nov. (♀, from Sudan). Lectotypes are designated for two species: S. albopunctatus Caporiacco, 1949 (♂) from Kenya and S. werneri Simon, 1906 (♀) from South Sudan. Six new combinations are proposed: Aelurillus ambiguus (Denis, 1966), comb. nov. (ex Stenaelurillus); Evarcha werneri (Simon, 1906), comb. nov. (ex Stenaelurillus); Phlegra davidi (Caleb, Mungkung & Mathai, 2015), comb. nov. (ex Mashonarus); Stenaelurillus brandbergensis (Wesołowska, 2006), comb. nov. (ex Mashonarus); Stenaelurillus guttatus (Wesołowska & Cumming, 2002), comb. nov. (ex Mashonarus); and S. termitophagus (Wesołowska & Cumming, 1999), comb. nov. (ex Microheros). Two species names are synonymized: Evarcha elegans Wesołowska & Russell-Smith, 2000 with E. werneri comb. nov.; and Aelurillus sahariensis Berland & Millot, 1941 with Stenaelurillus nigricaudus Simon
Parasitoid wasps new to Britain (Hymenoptera: Platygastridae,
Eurytomidae, Braconidae & Bethylidae)
(2014)
One genus and five species are recorded as new to Britain: Fidiobia, Fidiobia hispanica, Macroteleia bicolora (Platygastridae); Sycophila binotata (Eurytomidae); Schizoprymnus collaris (Braconidae); and Laelius pedatus (Bethylidae). Keys to British Macroteleia and Laelius are provided.
Provisional synonymy is proposed between Macroteleia minor and M. brevigaster, and synonymy is proposed between Laelius femoralis, L. microneurus and L. nigricrus. The possible mode of introduction of Sycophila binotata is discussed. A lectotype is designated for Schizoprymnus collaris.
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”.
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.
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
Bees of the genus Lasioglossum (Hymenoptera: Halictidae) from Greater Puerto Rico, West Indies
(2018)
The species of Lasioglossum from Greater Puerto Rico are reviewed. Nine species are recognized, including five new species described herein: asioglossum (Dialictus) genaroi sp. nov., L. (D.) dispersum sp. nov., L. (D.) enatum sp. nov., L. (D.) monense sp. nov. and L. (D.) amona sp. nov. The latter two are known only from Mona Island. Keys and images are provided to assist in identification. Details of nesting biology, floral hosts and distribution are provided where available. Three species, L. (D.) parvum (Cresson, 1865), L. (D.) busckiellum (Cockerell, 1915), and L. (D.) mestrei (Baker, 1906) are removed from the list of species for Puerto Rico. Details on their revised distribution are provided. Three new records for Haiti, L. (D.) gundlachii (Baker, 1906), L. (D.) ferrerii (Baker, 1906) and L. (D.) busckiellum are documented. Notes on other species in the Greater Antilles are provided, including the synonymy of Lasioglossum bruesi (Cockerell, 1912) and L. jamaicae (Ellis, 1914) under L. gemmatum (Smith, 1853).
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.
Within the tribe Coelidiini, subfamily Coelidiinae (Cicadellidae: Hemiptera), fragmentation of the genera Calodia Nielson, Olidiana McKamey and Taharana Nielson established the following 13 new genera: Cladolidia, type-species, Lodiana cladopenis Zhang; Creberulidia, type-species, Calodia paucita Nielson; Glaberana, type-species, Glaberana spadix, sp. nov.; Hamusolidia, type-species, Hamusolidia introrsa, sp. nov.; Hiatusorus, typespecies, Taharana schonhorsti Nielson; Laosolidia, type-species, Laosolidia complexa, sp. nov.; Orbisolidia, typespecies, Calodia spinocava Nielson; Singillatus, type-species, Lodiana furcata Nielson; Trinoridia, type-species, Trinoridia calcaris, sp. nov.; Tripesidia, type-species, Calodia warei Nielson; Tumidorus, type-species, Lodiana nielsoni Zhang; Webbolidia, type-species, Taharana webbi Nielson and Zhangolidia, type-species, Lodiana polyspinata Zhang. Nineteen genera in the tribe are treated.
The following 62 new species in 12 genera are described, illustrated and photographed: Calodia bicompressa (India); C. birama (Philippines); C. propennata (India); C. sichuanensis (China); C. sinuata (Laos); C. vincula (China, Vietnam); Creberulidia corniger (Laos); C. inflata (Thailand); C. multipenicula (Cambodia); C. ordospinosa (Thailand); C. penicula (Thailand); Glaberana ampla (Thailand); G. dentilamina (Thailand); G. longilamina (Thailand); G. penita (Laos); G. spadix (Laos); G. stylafurcata (Indonesia); Hamusolidia introrsa (Laos); Hiatusorus aviformus (Laos); H. robustus (China); H. supraspinosus (Thailand); Laosolidia complexa (Laos); L. tuberis (Laos); L. longiserrata (Laos); Olidiana tuberis (Vietnam); O. bispiculata (Laos); O. filiata (Thailand); O. implicata (Thailand); O. inaequabilia (Thailand); O. lata (Laos); O. parafringa (Laos); O. pennata (Laos); O. tonkinensis (Vietnam); O. vincula (Vietnam); Singillatus gracilius (Indonesia); S. ventrospinatus (India); Taharana abstrusa (Thailand); T. angusta (Vietnam); T. biavicula (Thailand); T. biunca (Thailand); T. brevicutata (Thailand); T. caverna (Malaysia); T. exiquitas (Thailand); T. forcipia (Thailand); T. gracilata (Thailand); T. incisura (Thailand); T. intimacalcara (Thailand); T. lacertosa (Thailand); T. mediolata (Thailand); T. minutura (Thailand); T. oblongiserrata (Laos); T. subspinata (Thailand); T. sublamina (Thailand); T. phetchahabunesis (Thailand); T. protriangulata (Thailand); T. subtumida (Thailand); T. truncata (Thailand); Trinoridia calcaris (India); T. trifida (Malaysia); Tripesidia kubani (Laos); Webbolidia kristenseni (Thailand); W. magna (Laos).
Taxonomy of all the genera is elucidated with a revised key to genera and species. The following formerly suppressed species are herein reinstated: Olidiana (Lodiana) flavofasciana Li, 1989, Olidiana (Lodiana) nigritibiana Li, 1987, Olidiana rufofasciana Li and Wang, 1989 and Webbolidia (Taharana) uniaristata Zhang, 1990. The following 3 species are new junior synonyms: Calodia flavinota Cai and Kuoh, 1993: 220 [= Calodia patricia (Jacobi), 1944:49], Olidiana yangi McKamey 2006: 502 [= Lodiana (Olidiana) hamularis Xu, 2000: 220] and Taharana yinggenensis Zhang and Zhang, 1994: 96 [= Taharana (Coelidia) sparsa (Stål) 1854: 254]. Taharana hainana Zhang 1994: 132 is a nomen nudum based on the same name in Zhang’s thesis (1988) which name was cited later by Li and Wang 1991: 275. Lodiana hainana Cai and He 2002: 139 is also a nomen nudum. A replacement name proposed herein is caii, nom. nov. in the genus Olidiana; Zhang’s 1994: 71 illustrations of subgenital plate (I) and aedeagus (M) of “fasciana Li” does not appear to represent the respective illustrations in Li 1991: 357 and may represent a new species in the genus Glaberana. The name of Olidiana nigridorsum (Cai and Shen) is changed to Olidiana nigridorsa (Cai and Shen) to agree with gender. Among 12 genera, 102 species are proposed in new combinations. Lodiana reductusi Xu and Kuoh, 1997 and Lodiana spicata Xu and Kuoh, 1997 are declared incertae sedis after attempts failed to locate the original descriptions and type specimens. Both species are provisionally assigned to the genus Olidiana. Two syntype specimens of Jassus egregius Schumacher, previously thought to be lost, were located in the Senckenberg Deutsches Entomologisches Institut, Müncheberg, Germany. The male specimen is designated lectotype herein. Six species in the Olidiana brevis (Walker) interspecific variation complex are elucidated with illustrations of male genitalia features.
New records, an updated checklist and a synoptic catalogue are also provided. All taxa including 264 valid species and 304 names are indexed.
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).
Indian spider species currently assigned to Storena Walckenaer, 1805 are revised mostly based on the type material available in the National Zoological Collection, Zoological Survey of India, Kolkata. A new genus, Laminion gen. nov. is proposed to include four species; three are transferred from Storena: Laminion arakuensis (Patel & Reddy, 1989) gen. et comb. nov., Laminion birenifer (Gravely, 1921) gen. et comb. nov. and Laminion debasrae (Biswas & Biswas, 1992) gen. et comb. nov., whereas the fourth species is from Suffasia Jocqué, 1991: Laminion gujaratensis (Tikader & Patel, 1975) gen. et comb. nov. The species Storena tikaderi Patel & Reddy, 1989 syn. nov. is synonymised with L. birenifer gen. et comb. nov. Storena dibangensis Biswas & Biswas, 2006 and Storena indica Tikader & Patel, 1975 are transferred to Mallinella Strand, 1906. All the type material examined are imaged and redescribed. In addition, images of the type material of Storenomorpha joyaus (Tikader, 1970) are presented.