Generic Reclassification of Limonius Eschscholtz, 1829 (Elateridae: Dendrometrinae) sensu Candèze 1860 of the World

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. 

1979 ◽  
Vol 111 (8) ◽  
pp. 949-954 ◽  
Author(s):  
Leonard A. Kelton

AbstractBrooksella n. gen. is described (type-species, Asciodema inconspicua Uhler). Lectotypes are designated for Asciodema inconspicua Uhler and Orthotylus viridicatus Uhler. The following North American species currently in Melanotrichus Reuter are transferred to Brooksella: Asciodema inconspicua Uhler (= M. atricornis Knight, n. syn.), M. chelifer Knight (= M. brevirostris Knight, M. custeri Knight, n. syn.), M. azteci Knight, M. incurvus Knight, M. malvastri Knight, M. nevadensis Knight, M. nicholi Knight, M. shoshonea Knight, Orthotylus althaeae Hussey, O. ferox Van Duzee, O. tibialis Van Duzee, and O. viridicatus Uhler. Male genitalia and tergal process are illustrated for each species and a key to separate them is provided.


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.


1935 ◽  
Vol 67 (1) ◽  
pp. 15-18
Author(s):  
Eric Hearle

In 1929 the writer described a British Columbian blackfly pupa with most unusual characteristics—unique among North American species in that the customary slender respiratory filaments are replaced by a closed, ringed, club-like horn with tw-o short, curved basal spurs. An examination of the literature at our disposal of the pupae known from Europe, Africa, Asia, Australasia and South America, indicates that a number of other unusual forms have been described, especially from Africa. Although the valid species of Simuliidae in the world fauna probably number more than three hundred and fifty, only about twelve of the known pupae of which we have records have breathing organs that are not of the filamentous type. In Northern Europe, Simulium equinum L., as described by Edwards and Puri, has breathing organs consisting of wide, thin-walled tubes, the basal and main branches of which form a ring on the thorax.


1979 ◽  
Vol 111 (2) ◽  
pp. 127-141 ◽  
Author(s):  
K.G.A. Hamilton

AbstractKeys are provided to the five genera and 12 species of Philaenini in North America. Philaenus (Stål) is redefined to include only two species, one of which, spumarius L., 1758 (= rubra Capanni, 1894, = aurata Capanni, 1894, new synonymies) is represented in North America by three introduced subspecies: quadrimaculatus (Sch.) in eastern and western continental America, spumarius s.s. in Newfoundland, and tesselatus (Mel.) from one locality in southern Ontario. Philaenus parallels Stearns is removed to Paraphilaenus Vilb. as its sole Nearctic representative (new combination) and Philaenus lineatus (L.) belongs to the distinctive genus Neophilaenus Hpt. Philaronia Ball is represented in North America by five species: abjecta (Uhl.), canadensis (Wal.), fuscovaria (Stål) new combination, pauca n. sp. and superba n. sp. Philaenarcys new genus includes three species: bilineata (Say), 1831, new combination (= Ptyelus basivitta Wlk., 1851, new synonymy), killa n. sp., and spartina n. sp.


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 ◽  
2019 ◽  
Vol 4671 (2) ◽  
pp. 195-222 ◽  
Author(s):  
JOHN W. BROWN

Seven new genera of North American Cochylina are described and illustrated: Anacochylidia Brown, new genus (type species: Anacochylidia maderana Brown, new species); Atroposia Pogue, new genus (type species: Conchylis oenotherana Riley, 1881), resulting in Atroposia oenotherana (Riley), new combination; Cagiva Pogue, new genus (type species: Phalonia cephalanthana Heinrich, 1921), resulting in Cagiva cephalanthana (Heinrich), new combination; Cybilla Pogue, new genus (type species: Phalonia hubbardana Busck, 1907), resulting in Cybilla hubbardana (Busck), new combination; Honca Pogue, new genus (type species: Phalonia grandis Busck, 1907), resulting in Honca grandis (Busck), new combination; Nycthia Pogue, new genus (type species: Phalonia pimana Busck, 1907), resulting in Nycthia pimana (Busck), new combination, and N. yuccatana (Busck, 1907), new combination; and Pogospinia Brown, new genus (type species: Pogospinia floridana Brown, new species), with three new combinations: Pogospinia spinifera (Razowski, 1967), new combination; P. veracruzanus (Razowski and Becker, 1986); new combination, and P. signata (Razowski, 1967), new combination. The Palearctic genus Cochylichroa Obraztsov & Swatschek, 1958, revised status (type species: Eupoecilia atricapitana Stephens, 1852), is redefined based on North American congeners, resulting in the following new combinations: Cochylichroa arthuri (Dang, 1984), new combination; C. atricapitana (Stephens, 1852), revised status; C. aurorana (Kearfott, 1907), new combination; C. avita (Razowski, 1997), new combination; C. foxcana (Kearfott, 1907), new combination; C. hospes (Walsingham, 1884), new combination; C. hoffmanana (Kearfott, 1907), new combination; C. temerana (Busck, 1907), new combination; and C. viscana (Kearfott, 1907), new combination. Monoceratuncus Razowski, 1992, is reported for the first time from the U.S.A. as Monoceratuncus lantana Pogue, new species. Mimcochylis Razowski, 1985, is reported for the first time from the U.S.A. as Mimcochylis fulvotinctana (Walsingham, 1884), new combination and senior synonym of M. planola Razowski, 1985, new synonym. One new species is described in Aethes Billberg, 1820 (i.e., A. triassumenta Pogue, new species), and one new combination (i.e., A. ringsi (Metzler, 2000), new combination, is proposed. Two other new combinations are proposed: Thyraylia wiscana (Kearfott, 1907), new combination, and Eupinivora parotanus (Razowski and Becker, 2010), new combination. 


1967 ◽  
Vol 45 (7) ◽  
pp. 1041-1046 ◽  
Author(s):  
Margaret E. Barr

This report on the occurrence of a number of western North American species of Loculoascomycetes includes the new combinations and the new name: Wettsteinina andromedae var. cassiopes (Dearn and House) Barr, W. sieversiae (Peck) Barr, and Leptosphaeria hesperia Barr.


1978 ◽  
Vol 9 (1) ◽  
pp. 75-76
Author(s):  
Leif Lyneborg

AbstractNeotherevella n.gen. is proposed as a replacement for Neothereva Kröber sensu Lyneborg (1976). Neothereva Kröber, 1912, is placed in new synonymy with Thereva Latreille, 1796, as the consequence of an overlooked designation of a type-species for Neothereva Kröber, 1912, by Kröber (1935). Neotherevella is fully described. Five specific names are placed in new combination with Neotherevella, which is known from Namibia, Mauritania, Algeria, Sudan, Egypt, Israel, Uzbechistan and Mongolia. It is demonstrated that two species described in combination with Neothereva by Zaitzev (1970) do not belong to Neotherevella.


1961 ◽  
Vol 39 (1) ◽  
pp. 21-33 ◽  
Author(s):  
C. Frankton ◽  
R. J. Moore

The morphology and specific differences of Cirsium undulatum (Nutt.) Spreng. and of C. flodmanii (Rydb.) Arthur are described and their Canadian distributions are reported in detail. The chromosome numbers are C. undulatum f. undulatum and f. album Farwell, 2n = 26; C. flodmanii f. flodmanii and f. albiflorum D. Löve, 2n = 22. The origin of four North American species of Cirsium that do not follow the world-wide base number 17 is discussed; it is postulated that reduction in number has occurred by translocations. The chromosomes of species with reduced numbers are larger than those of the unreduced species but the total length of the chromosomes of both groups is approximately the same.


Botany ◽  
2016 ◽  
Vol 94 (10) ◽  
pp. 917-939 ◽  
Author(s):  
Amanda M. Savoie ◽  
Gary W. Saunders

Sequence data (COI-5P and rbcL) for North American members of the tribe Pterosiphonieae were compared with collections from around the world. Phylogenetic analyses resolved Pterosiphonia as polyphyletic and many species required transfer to other genera. In our analyses Pterosiphonia sensu stricto included only the type species P. cloiophylla (C. Agardh) Falkenberg and P. complanata (Clemente) Falkenberg, as well as the South African species P. stegengae sp. nov. A new genus, Xiphosiphonia gen. nov., was described for X. ardreana (Maggs & Hommersand) comb. nov., X. pennata (C. Agardh) comb. nov., and X. pinnulata (Kützing) comb. nov. Some Asian, European and North American species previously attributed to Pterosiphonia were transferred to Symphyocladia including S. baileyi (Harvey) comb. nov., S. dendroidea (Montagne) comb. nov., S. plumosa nom. nov. (for P. gracilis Kylin), and S. tanakae (S. Uwai & M. Masuda) comb. nov. We also described two new North American species, Symphyocladia brevicaulis sp. nov. and S. rosea sp. nov. Other species formed a well-supported clade for which the genus name Polyostea Ruprecht was resurrected. Included in Polyostea were P. arctica (J. Agardh) comb. nov., P. bipinnata (Postels & Ruprecht) Ruprecht, P. hamata (E.S. Sinova) comb. nov., and P. robusta (N.L. Gardner) comb. nov.


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