scholarly journals Resolution of some taxonomic and nomenclatural issues in a recent revision of Ceraeochrysa (Neuroptera: Chrysopidae)

Zootaxa ◽  
2010 ◽  
Vol 2565 (1) ◽  
pp. 55 ◽  
Author(s):  
CATHERINE A. TAUBER ◽  
OLIVER S. FLINT, JR.

With the purpose of promoting nomenclatural stability, this paper addresses a number of errors, omissions, and controversial conclusions in a recent revision of the green lacewing genus Ceraeochrysa by Freitas et al. (2009). 1. Valid species, new combinations and synonymies: (a) We identified Ceraeochrysa chiricahuae Freitas and Penny (in Freitas et al. 2009), Chrysopa forreri Navás, and Chrysopa intacta Navás as subjective synonyms. Thus, Ceraeochrysa intacta, a species that was previously synonymized under Ceraeochrysa placita (Banks), becomes the valid name of the species [New status, new combination]. Chrysopa forreri is now synonymized under Cer. intacta, not Cer. placita [New synonymy]. And, Cer. chiricahuae becomes a junior synonym of Cer. intacta, not a valid species of Ceraeochrysa [New synonymy]. (b) We enumerate specific internal and external features of the Chrysopa cornuta Navás type that identify it as conspecific with Ceraeochrysa caligata (Banks), not Ceraeochrysa cincta (Schneider) as proposed by Freitas et al. (2009). Thus, Ceraeochrysa cornuta (Navás), which has priority, is reinstated as the valid name [Reinstated status, reinstated combination], and Ceraeochrysa caligata (Banks) is reinstated as a junior subjective synonym of Cer. cornuta, not a valid species [Reinstated synonymy]. (c) We provide documented evidence for reinstating three synonymies that Freitas et al. had reversed [Reinstated synonymies]: (i) Allochrysa parvula Banks is a junior subjective synonym of Ceraeochrysa lineaticornis (Fitch); (ii) Chrysopa columbiana Banks is a junior subjective synonym of Ceraeochrysa lineaticornis (Fitch); (iii) Chrysopa rochina (Navás) is a junior subjective synonym of Ceraeochrysa cincta (Schneider). 2. Generic assignments: (a) Visual evidence is provided for the placement of Ceraeochrysa laufferi (Navás) in Ungla. Therefore, Ungla laufferi (Navás) is reinstated as the valid name [Reinstated combination]. (b) We question Freitas et al.’s rationale for including Cer. placita (Banks) and Cer. intacta (Navás) (as Cer. chiricahuae Freitas and Penny) in the genus Ceraeochrysa; female and larval features of the two species differ markedly from those used to characterize Ceraeochrysa species. As an alternative that recognizes the uncertainty surrounding the generic placement of these species and that avoids additional, unnecessary name changes, we propose including the caveat “genus incertae sedis” with the names, as follows: Ceraeochrysa placita (Banks), genus incertae sedis, and Ceraeochrysa intacta (Navás), genus incertae sedis. 3. Type designations: (a) Errors concerning the Chrysopa furculata Navás type in the Muséum national d’Histoire naturelle, Paris (MNHN), are corrected, and doubts raised by Freitas et al. (2009) concerning the identification of this specimen as the holotype are removed. (b) The earlier designation of the Chrysopa rochina (Navás) type in the MNHN as the lectotype (not holotype) is verified.

Zootaxa ◽  
2019 ◽  
Vol 4683 (3) ◽  
pp. 301-335 ◽  
Author(s):  
FRANK E. ETZLER

The genus Limonius Eschscholtz, 1829 was last treated as a whole by Candèze (1860). Since then, members have been placed in eight other genera: Cidnopus Thomson, 1859; Gambrinus LeConte, 1853; Elathous Reitter, 1890; Kibunea Kishii, 1966; Limoniscus Reitter, 1905; Nothodes LeConte, 1861; Pheletes Kiesenwetter, 1858; and Solskyana Dolin, 1978. Based on the examination of adult and larval characters, five genera are recognized: Elathous Reitter, 1890; Gambrinus LeConte, 1853; Limonius Eschscholtz, 1829; Pheletes Kiesenwetter, 1858; and Tetralimonius new genus. Limoniscus Reitter, 1905 and Sichuanelater Platia and Gudenzi, 2006 are new synonymies of Gambrinus LeConte, 1853; Micrathous Lane, 1971, Neoathousius Schimmel and Platia, 1991 and Solskyana Dolin, 1978 are all new synonymies of Limonius. A total of 84 new combinations are proposed: Nearctic: Elathous huguenini (Van Dyke, 1932) new combination; Gambrinus angulatus (Motschulsky, 1859) new combination; Gambrinus bicolor (Van Dyke, 1932) new combination; Gambrinus clypeatus (Motschulsky, 1859) new combination; Gambrinus confusus (LeConte, 1853) new combination; Gambrinus cribriceps (Van Dyke, 1943) new combination; Gambrinus crotchii (Horn, 1872) new combination; Gambrinus flavomarginatus (Knull, 1938) new combination; Gambrinus fulvipilis (Candèze, 1860) new combination; Gambrinus griseus (Beauvois, 1805) new combination; Gambrinus humidus (Lane, 1941) new combination; Gambrinus interstitialis (Melsheimer, 1846) new combination; Gambrinus lanchesteri (Lane, 1941) new combination; Gambrinus meridianus (Knull, 1947) new combination; Gambrinus mirus (LeConte, 1853) new combination; Gambrinus norahae (Al Dhafer, 2009) new combination; Gambrinus olentangyi (Knull, 1947) new combination; Gambrinus plebejus (Say, 1825) new combination; Gambrinus propexus (Candèze, 1860) new combination; Gambrinus rudis (Brown, 1933) new combination; Gambrinus rufihumeralis (Lane, 1941) new combination; Gambrinus seminudus (Van Dyke, 1932) new combination; Gambrinus shircki (Lane, 1965) new combination; Gambrinus sinuifrons (Fall, 1907) new combination; Gambrinus snakensis (Lane, 1965) new combination; Gambrinus stigma (Herbst, 1806) new combination; Gambrinus pictus (Van Dyke, 1932) new combination; Gambrinus ulkei (Horn, 1871) new combination; Gambrinus ursinus (Van Dyke, 1932) new combination; Gambrinus venablesi (Wickham, 1913) new combination; Limonius brevis (Van Dyke, 1932) new combination; Limonius sordidus (Van Dyke, 1932) new combination; Pheletes lecontei (Lane, 1971) new combination; Tetralimonius definitus (Ziegler, 1845) new combination; Tetralimonius humeralis (Candèze, 1860) new combination; Tetralimonius maculicollis (Motschulsky, 1860) new combination; Tetralimonius nimbatus (Say, 1825) new combination; Tetralimonius ornatulus (LeConte, 1857) new combination. Palearctic: Gambrinus elegans (Buysson, 1891) new combination; Gambrinus gibbosus (Platia and Gudenzi, 2006) new combination. Gambrinus henanensis (Schimmel, 2006) new combination; Gambrinus hinakurai (Kishii, 1998) new combination; Gambrinus katoi (Kishii, 2002) new combination; Gambrinus kawaharai (Kishii, 2002) new combination; Gambrinus kucerai (Schimmel, 2006) new combination; Gambrinus nanshanensis (Arimoto and Hiramatsu, 2013) new combination; Gambrinus naomii (Kishii, 1997) new combination; Gambrinus shaanxiensis (Schimmel, 2006) new combination; Gambrinus suturalis (Gebler, 1844) new combination; Gambrinus takabai (Kishii, 1997) new combination; Gambrinus violaceus (Müller, 1821) new combination; Gambrinus wittmeri (Chassain, 1998) new combination; Gambrinus yamato (Kishii, 1998) new combination; Gambrinus yujii (Arimoto, 2013) new combination; Gambrinus zhejiangensis (Schimmel, 2015) new combination; Limonius brancuccii (Schimmel and Platia, 1991) new combination; Limonius decorus (Gurjeva, 1975) new combination; Limonius exiguus (Schimmel and Platia, 1991) new combination; Limonius hartmanni (Schimmel, 1998) new combination; Limonius hiermeieri (Schimmel and Platia, 1991) new combination; Limonius hirtus (Dolin, 1978) new combination; Limonius hubeiensis (Kishii and Jiang, 1996) new combination; Limonius kubani (Schimmel, 1996) new combination; Limonius loebli (Schimmel and Platia, 1991) new combination; Limonius longicornis (Schimmel and Platia, 1991) new combination; Limonius macedonicus (Cate and Platia, 1989) new combination; Limonius marginellus brusteli (Leseigneur, 2004) new combination; Limonius manaliensis (Schimmel and Platia, 1991) new combination; Limonius miandamensis (Schimmel and Platia, 1991) new combination; Limonius minusculus (Schimmel and Platia, 1991) new combination; Limonius nigronitidus (Han and Lee, 2012) new combination; Limonius platiai (Mertlik, 1996) new combination; Limonius pseudopilosus (Platia and Gudenzi 1985) new combination; Limonius recticornis (Schimmel and Platia, 1991) new combination; Limonius riesei (Platia, 1988) new combination; Limonius rusticus (Schimmel and Platia, 1991) new combination; Limonius schurmanni (Platia and Gudenzi, 1998) new combination; Limonius sinensis (Schimmel and Platia, 1994) new combination; Limonius singularis (Schimmeland Platia, 1991) new combination; Limonius stapfi (Schimmel, 2007) new combination; Limonius turcicus (Platia, 2004) new combination; Limonius wittmeri (Schimmel and Platia, 1991) new combination; Tetralimonius quercus (Olivier, 1790) new combination; Tetralimonius reitteri (Gurjeva, 1976) new combination. The following 12 North American species are removed from synonymy and recognized as valid species: Gambrinus interstitialis (Melsheimer, 1846) status resurrected; Gambrinus propexus (Candèze, 1860) status resurrected; Gambrinus shircki (Lane, 1965) status resurrected; Gambrinus snakensis (Lane, 1965) status resurrected; Gambrinus ulkei (Horn, 1871) status resurrected; Limonius anceps LeConte, 1853 status resurrected; Limonius dubitans LeConte, 1853 status resurrected; Limonius infuscatus Motschulsky, 1859 status resurrected; Limonius pilosulus Candèze, 1891 status resurrected; Limonis semianeus LeConte, 1853 status resurrected. Tetralimonius humeralis (Candèze, 1860) status resurrected; Tetralimonius maculicollis (Motschulsky, 1860) status resurrected. New replacement names are proposed for three homynyms: Limonius schimmeli Etzler new name for Neoathousius ferrugineus Schimmel and Platia, 1991; Elathous malatyanus Etzler new name for Elathous bicolor Platia, 2010, not Elathous bicolor (LeConte, 1853); and Microdesmes carteri Etzler new name for Limonius angulatus Carter, 1939 (= Microdesmes angulatus). Limonius kondratieffi Al Dhafer, 2009 is a new synonymy of Elathous bicolor (LeConte, 1853). A key to genera, generic descriptions, notes on species, and definitions of important characters are provided. 


Zootaxa ◽  
2021 ◽  
Vol 4966 (2) ◽  
pp. 215-225
Author(s):  
LAURA BREITKREUZ ◽  
PETER DUELLI ◽  
JOHN OSWALD

Apertochrysa Tjeder, 1966, is identified as a new senior subjective synonym of the large, subcosmopolitan, green lacewing genus currently known under the name Pseudomallada Tsukaguchi, 1995. Apertochrysa is rediagnosed and the taxonomic consequences of the new synonymy are reviewed. New combinations are created in Apertochrysa for 165 species formerly placed in Pseudomallada and for two species formerly placed in Mallada; three species are transferred from Pseudomallada back to previously-established combinations in Apertochrysa; and 13 additional species are retained in Apertochrysa from previous placements. This brings the total number of Apertochrysa species to 183. 


Zootaxa ◽  
2012 ◽  
Vol 3376 (1) ◽  
pp. 1 ◽  
Author(s):  
MAR FERRER-SUAY ◽  
JORDI PARETAS-MARTÍNEZ ◽  
JESÚS SELFA ◽  
JULI PUJADE-VILLAR

The Charipinae (Cynipoidea: Figitidae) are a small group of Hymenoptera biologically characterized as being secondary parasitoids of aphids and psyllids (Hemiptera) (Menke & Evenhuis, 1991).  A total of 281 species of Charipinae have been described since the first species was described by Westwood (1833) (including two fossils, one of them recently transferred in a new family, Protimaspidae). An updated world catalogue of the Charipinae is presented here, with 168 valid species: 111 included in Alloxysta Förster, 31 in Phaenoglyphis Förster, 13 in Dilyta Förster, 5 in Apocharips Fergusson, 4 in Thoreauana Girault, and 1 in Dilapothor Paretas-Martínez & Pujade-Villar, Lobopterocharips Paretas-Martínez & Pujade-Villar, Lytoxysta Kieffer and †Protocharips Kovalev. Eight species are considered as nomen nudum: Allotria fusca Dahlbom, 1842; Allotria thoreyi Dahlbom, 1842; Xystus xanthocephala Dahlbom, 1842; Allotria pusillina Giraud, 1877; Charips aphidiinaecida de Santis, 1937; Alloxysta keudelli Hedicke, 1927; Allotria amygdali Buckton, 1879 and  Allotria polita Provancher, 1881. Six as nomen dubium: Allotria (Allotria) recticornis atra Kieffer, 1902; Allotria (Allotria) brevicornis Kieffer, 1902;  Allotria (Allotria) orthocera Kieffer, 1902; Xystus femoralis Hartig, 1841; Charipsella laevigata Brèthes, 1913; Dilyta (Alloxysta) ignorata Kieffer, 1900. Three species are incertae sedis: Charips silvicola Belizin, 1928, Cynips atriceps Buckton, 1879 and Allotria (Allotria) testaceipes Kieffer, 1902. Two species are here synonymized: Alloxysta discreta (Förster, 1869) with A. ramulifera (Thomson, 1862) and A. megaptera (Cameron, 1889) with A. ruficollis (Cameron, 1883). Two species are raised from synonymy and considered here as valid species: Alloxysta cameroni (Cameron, 1883) and A. marshalliana (Kieffer, 1900). New names for species of Alloxysta are presented for homonimies with other Alloxysta species derived from the new combinations: Alloxysta ionescui Pujade-Villar & Ferrer-Suay new name for Alloxysta luteipes (Ionescu, 1969) n. comb., Alloxysta forshagei Pujade-Villar & Ferrer-Suay new name for Alloxysta bicolor (Ionescu, 1959) n. comb., and Alloxysta mattiasi Pujade-Villar & Ferrer-Suay new name for Alloxysta luteipes (Ionescu, 1959) n. comb. Also a new name to Phaenoglyphis is presented for the same reason before mentioned but without new combination: Phaenoglyphis hedickei Pujade-Villar & Ferrer-Suay new name for Phaenoglyphis longicornis Hedicke, 1928 and two new combinations are presented: Alloxysta rufa (Ionescu, 1959) n. comb and Alloxysta consobrina (Zetterstedt, 1838) Forshage n. comb. This catalogue includes: (i) a diagnosis of the subfamily with the most important taxonomic characters for species recognition, and illustrations of these characters; (ii) a key to genera; (iii) a list of all authors describing species of Charipinae; and (iv) a host table. The distribution of the Charipinae includes 106 Palaearctic species, 37 Nearctic, 11 Neotropical, 10 Afrotropical, 7 Oriental and 11 Australian. The species Alloxysta victrix (Westwood, 1833), A. fuscicornis (Hartig, 1841) and Phaenoglyphis villosa (Hartig, 1841) are cosmopolitan.


Zootaxa ◽  
2021 ◽  
Vol 4966 (2) ◽  
pp. 127-144
Author(s):  
VASILISA G. CHEMYREVA ◽  
DAVID G. NOTTON ◽  
ALEJANDRO ZALDÍVAR-RIVERÓN

A revision of the Palaearctic species of the genus Idiotypa Förster is provided. The genus Eunuchopria Szabó, 1961 is a junior synonym of Idiotypa Förster, 1856 syn. n. and the new combination Idiotypa nitens (Szabó, 1961) comb. n., is established. Dublicate original spellings I. marii and I. mariae are resolved by first reviser action; I. mariae is now the correct original spelling. Lectotypes are designated for Idiotypa mariae and I. maritima. New synonymy is proposed: I. maritima (Haliday, 1833) = I. rufiventris (Thomson, 1858) syn. n.; = I. nigriceps Kieffer, 1909 syn. n.; = I. nigriceps Kieffer, 1911 syn. n. The three valid species I. mariae Gregor, 1939, I. maritima (Haliday, 1833) and I. nitens (Szabó, 1961) are redescribed, illustrated and keyed. 


Zootaxa ◽  
2019 ◽  
Vol 4613 (2) ◽  
pp. 327
Author(s):  
LAURENCE A. MOUND ◽  
DESLEY J. TREE

The genus Xylaplothrips is re-diagnosed, 11 species are listed as appropriately included in this genus of which three are new combinations from Haplothrips (X. acaciae; X. collyerae; X. gahniae). A further six species are listed as incertae sedis within Xylaplothrips and a key is provided to the four species of this genus known from Australia including X. anarsius sp.n. The genus Mesandrothrips is recalled from synonymy with Xylaplothrips, and a list is provided of 20 appropriately included species of which 14 are new combinations from Xylaplothrips (M. caliginosus; M. clavipes; M. darci; M. dubius; M. emineus; M. flavitibia; M. flavus; M. inquilinus; M. montanus; M. pictipes; M. pusillus; M. reedi; M. subterraneus; M. tener), and one is a new combination from Haplothrips (M. inquinatus). A key is provided to 10 species of this genus known from Australia, including three species transferred from Haplothrips, together with M. austrosteensia sp.n., M. googongi sp.n., M. kurandae sp.n., M. lamingtoni sp.n. and M. oleariae sp.n. The type species, M. inquilinus, is widespread across Southeast Asia as an invader of thrips galls, and Haplothrips darci Girault based on a single female from Queensland is considered closely related. 


Zootaxa ◽  
2018 ◽  
Vol 4449 (1) ◽  
pp. 1 ◽  
Author(s):  
MARIANA CHANI-POSSE ◽  
ALFRED F. NEWTON ◽  
ASLAK KAPPEL HANSEN ◽  
ALEXEY SOLODOVNIKOV

A checklist of all described species of Philonthina, a subtribe of the staphylinid tribe Staphylinini, known to occur in Central and South America (CASA) is presented. Included for each species, and for synonyms known from CASA, is a reference to the original description, type locality and type depository, and for each species the known distribution within and outside CASA. Type material was sought in the main European and American collections where it is deposited (BMNH, MNHUB, IRSNB and FMNH) and is summarized for all indigenous CASA species, with lectotypes designated for 16 names and confirmation of holotypes and prior designation of lectotypes when necessary. Based on recent phylogenetic work in Philonthina and our revision of types of CASA species of Philonthus Stephens, 1829 and Belonuchus Nordmann, 1837, some taxonomic changes are proposed. Thirty-one species of Philonthus are transferred to Belonuchus (16), Gabrius Stephens 1829 (14), and Bisnius Stephens 1829 (one) resulting in the following new combinations: B. abnormalis (Sharp 1885), B. celatus (Sharp 1885), B. corticalis (Sharp 1885), B. extremus (Sharp 1885), B. infimus (Sharp 1885), B. iteratus (Sharp 1887), B. latecinctus (Sharp 1885), B. lucilius (Sharp 1885), B. muticus (Sharp 1876), B. optatus (Sharp 1885), B. platypterus (Sharp 1885), B. rufiventris (Sharp 1887), B. rufocaudus (Sharp 1885), B. rufopygus (Sharp 1885), B. serraticornis (Sharp 1876), B. supernus (Herman 2001), G. approximans (Sharp 1885), G. armatipes (Sharp 1885), G. atricolor (Sharp 1885), G. championi (Sharp 1885), G. dampfi (Bernhauer 1929), G. elegans (Sharp 1885), G. forsterianus (Scheerpeltz 1960), G. misellus (Sharp 1885), G. nugax (Sharp 1885), G. ovaticeps (Sharp 1885), G. peruvianus (Bernhauer 1916), G. planulatus (Sharp 1885), G. rusticus (Sharp 1885), G. serpens (Sharp 1885) and Bi. subaeneipennis (Bernhauer 1916). Endeius nitidipennis Solier 1849 is transferred to Gabrius, resulting in the following new combination, G. nitidipennis (Solier 1849). Leptopeltus carchiensis Chani-Posse & Asenjo 2013 is proposed as junior synonym of Philonthus divisus Sharp 1891, which is transferred to Leptopeltus Bernhauer 1906 resulting in a new combination: Leptopeltus divisus (Sharp 1891). Belonuchus penetrans Silvestri 1946 is transferred to Pridonius Blackwelder 1952 as a new combination. Lectotypes are designated for Atopocentrum mirabile Bernhauer 1906, Philonthus armatipes Sharp 1885, Ph. atricolor Sharp 1885, Ph. championi Sharp 1885, Ph. misellus Sharp 1885, Ph. planulatus Sharp 1885, Ph. rusticus Sharp 1885, Ph. serpens Sharp 1885, Ph. abnormalis Sharp 1885, Ph. celatus Sharp 1885, Ph. infimus Sharp 1885, Ph. latecinctus Sharp 1885, Ph. muticus Sharp 1876, Ph. platypterus Sharp 1885, Ph. rufocaudus Sharp 1885 and Ph. rufopygus Sharp 1885. Of the 543 currently known species of Philonthina reported from CASA, at least 14 are believed to be adventive from elsewhere, 56 may occur naturally elsewhere, and 473 (87%) are evidently endemic to this region. Of the 31 genera represented by these described species, 20 (65%) are endemic to CASA. One genus, Gabronthus Tottenham 1955, is adventive. However, the actual philonthine fauna of CASA will undoubtedly be much larger, and the generic composition highly modified, when the fauna is fully explored and studied within a phylogenetical framework. 


2021 ◽  
Vol 38 ◽  
pp. 1-22
Author(s):  
Rodrigo S. Bouzan ◽  
Luiz Felipe M. Iniesta ◽  
João Paulo P. Pena-Barbosa ◽  
Antonio D. Brescovit

This study concerns the diplopod genus Eucampesmella Schubart, 1955, widespread in Brazil. After this work, the genus includes 12 valid species, and three incertae sedis: E. pugiuncula (Schubart, 1946), E. brunnea Kraus, 1959 and E. schubarti Kraus, 1957. The type-species, Eucampesmella tricuspis (Attems, 1931), is redescribed based on the holotype, and the following six new Brazilian species are added: Eucampesmella macunaima sp. nov. from the states of Rondônia, Pará, and Piauí; E. capitu sp. nov. from the states of Piauí and Paraíba; E. brascubas sp. nov. from the state of Sergipe; E. iracema sp. nov. from the state of Pernambuco; E. pedrobala sp. nov. from the state of Ceará; and E. lalla sp. nov. from the state of Rio Grande do Norte. Furthermore, E. lartiguei ferrii (Schubart, 1956) is recognized as a junior synonym of E. lartiguei lartiguei (Silvestri, 1897), which also had its status changed, and E. sulcata (Attems, 1898) is revalidated, prevailing under the name Leptodesmus tuberculiporus Attems, 1898. In addition, drawings, diagnoses, and distribution maps for all species of the genus are provided.


Zootaxa ◽  
2021 ◽  
Vol 4985 (4) ◽  
Author(s):  
LIJIE CHEN ◽  
JICHUN XING

The soft scale insect genus Scythia (Hemiptera: Coccomorpha: Coccidae) was established by Kiritchenko (1938) with the type species Scythia craniumequinum Kiritchenko, 1938 from Ukraine. Later, Borchsenius (1957) placed Mohelnia Šulc, 1941 (type species: Mohelnia festuceti Šulc, 1941) as a junior subjective synonym of Scythia Kiritchenko, 1938, and proposed new combination: Scythia festuceti (Šulc, 1941). Ben-Dov (1993) followed Borchsenius (1957) in treating Mohelnia as a junior synonym of Scythia.


Zootaxa ◽  
2020 ◽  
Vol 4822 (1) ◽  
pp. 101-112
Author(s):  
YUNLONG MA ◽  
XINGKE YANG ◽  
XINGYUE LIU

A taxonomic study of the green lacewing genus Austrochrysa Esben-Petersen, 1928 from China is presented. Three species of Austrochrysa are recorded from China. Two new species, Austrochrysa lihongyui sp. nov. and Austrochrysa angusta sp. nov., which are described in this study, and a new combination, i.e. Austrochrysa tropica (Yang & Wang, 1994) comb. nov., is proposed. The genus Yunchrysopa Yang & Wang, 1994 is here considered as a junior synonym of Austrochrysa Esben-Petersen, 1928. 


Zootaxa ◽  
2019 ◽  
Vol 4655 (1) ◽  
pp. 1-104 ◽  
Author(s):  
ALLEN F. SANBORN

The known cicada fauna of Bolivia is identified. Adusella Haupt, 1918 rev. stat. is resurrected and redescribed being elevated from junior synonym status with Odopoea Stål, 1861. Edholmbergi Delétang, 1919 rev. stat, n. syn. is elevated from junior synonymy of Odopoea and synonymized with Adusella rev. stat. Adusella insignifera (Berg, 1879) n. comb., Adusella signata Haupt, 1918 n. comb., and Adusella venturii (Distant, 1906c) n. comb. are transferred or returned to Adusella rev. stat. Carineta bilineosa Walker 1858b rev. stat., Carineta obtusa Walker 1858b rev. stat., Carineta tenuistriga Walker 1858c rev. stat. and Carineta diplographa Berg 1879 rev. stat. are removed from junior synonymy with Carineta fasciculata (Germar, 1821). Carineta obtusa rev. stat., n. syn., Carineta tenuistriga rev. stat., n. syn. and Carineta diplographa Berg 1879 rev. stat., n. syn. are considered junior synonyms of Carineta bilineosa rev. stat. Carineta limpida Torres 1948a n. syn. is shown to be a junior synonym of Carineta fasciculata. Carineta turbida Jacobi, 1907 is transferred to the genus Herrera Distant, 1905c to become Herrera turbida (Jacobi, 1907) n. comb. The genera Diceroprocta Stål, 1870, Orialella Metcalf, 1952, Quesada Distant, 1905c, and Nosola Stål, 1866a are assigned to the Guyalnina Boulard & Martinelli, 1996 within the Fidicinini Distant, 1905d. Tympanoterpes virgulata n. sp., Cracenpsaltria nana n. sp., Guyalna dasyeia n. sp., Guyalna fasciata n. sp., Guyalna polypaga n. sp., Parnisa santacruzensis n. sp., Carineta ensifera n. sp., Carineta hamata n. sp., Carineta pictilis n. sp., Carineta uncinata n. sp., Herrera concolor n. sp., Herrera freiae n. sp., Herrera melanomesocranon n. sp., Herrera phyllodes n. sp., and Herrera signifera n. sp. are described as new. The first records of Adusella insignifera (Berg, 1879) n. comb., Adusella venturii (Distant, 1906c) n. comb., Fidicina christinae Boulard & Martinelli, 1996, Fidicina ethelae (Goding, 1925), Fidicina robini Boulard & Martinelli 1996, Fidicinoides descampsi Boulard & Martinelli, 1996, Fidicinoides pauliensis Boulard & Martinelli, 1996, Fidicinoides sucinalae Boulard & Martinelli, 1996, Proarna alalonga Sanborn & Heath, 2014, Proarna bergi (Distant, 1892a), Proarna grisea (Fabricius, 1775), Proarna guttulosa (Walker, 1858b), Proarna insignis Distant, 1881a, Proarna strigicollis Jacobi, 1907, Guyalna distanti (Goding, 1925) Guyalna glauca (Goding, 1925), Guyalna platyrhina Sanborn & Heath, 2014, Guyalna viridifemur (Walker, 1850), Majeorona lutea Distant, 1906d, Carineta bilineosa Walker 1858b rev. stat., Carineta cearana Distant, 1906c, Carineta detoulgoueti Champanhet, 2001, Carineta doxiptera Walker, 1858a, Carineta maculosa Torres, 1948a, Carineta pilifera Walker, 1858c, Carineta rufescens (Fabricius, 1803), Carineta tetraspila Jacobi, 1907, and Herrera turbida (Jacobi, 1907) n. comb. are provided. The records for Adusella insignifera (Berg, 1879) n. comb. and Adusella venturii (Distant, 1906c) n. comb. are the first records of the tribe Zammarini Distant, 1905b, subtribe Zammarina Distant, 1905a, and genus Adusella, Tympanoterpes virgulata n. sp. is the first record of the genus Tympanoterpes Stål, 1861, Majeorona lutea Distant, 1906d is the first record for the genus Majeorona Distant, 1905d, Parnisa santacruzensis n. sp. is the first record of the genus Parnisa Stål, 1862a for Bolivia, specimens in the type series of Cracenpsaltria nana n. sp. represent the first record of the genus Cracenpsaltria Sanborn, 2016c in Ecuador, and the specimens of Herrera concolor n. sp., Herrera freiae n. sp., Herrera melanomesocranon n. sp., Herrera phyllodes n. sp., and Herrera signifera n. sp., and Herrera turbida (Jacobi, 1907) n. comb. and the new combinations to the genus are the first records of the genus Herrera Distant, 1905c for Bolivia, Brazil, French Guiana, and Peru. New records are provided to expand the ranges of Proarna alalonga Sanborn & Heath, 2014 and Carineta gemella to include Paraguay, the range of Dorisiana noriegai Sanborn & Heath, 2014 to include Paraguay and French Guiana, the range of Guyalna platyrhina to include Brazil, and the range of Carineta cearana to include Colombia. Previous records of Proarna bufo Distant, 1905d and Carineta fasciculata (Germar, 1821) are considered to be misidentifications P. bergi (Distant, 1892a) and Carineta bilineosa Walker 1858b rev. stat. so that P. bufo and C. fasciculata are removed from the cicada fauna of Bolivia as is Hemisciera maculipennis (de Laporte, 1832) which is shown to have been mistakenly attributed to Bolivia and Argentina. The non-Bolivian Carineta criqualicae Boulard 1986a, Carineta guianaensis Sanborn, 2011a, Carineta quinimaculata Sanborn, 2011a, and Carineta tigrina Boulard 1986a are reassigned to the genus Herrera to become Herrera criqualicae (Boulard, 1986a) n. comb., Herrera guianaensis (Sanborn, 2011a) n. comb., Herrera quinimaculata (Sanborn, 2011a) n. comb., and Herrera tigrina (Boulard, 1986a) n. comb., respectively. A discussion on the species status of Carineta fasciculata (Germar, 1821) is provided to clarify the taxon along with the new synonymy. The currently known Bolivian cicada fauna is comprised of 83 described species from 21 genera, seven tribes and three subfamilies with the new records and new species presented here increasing the known fauna by 107.5%. 


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