Addenda and corrigenda to the "Annotated catalogue of the Laniatores of the New World (Arachnida, Opiliones)"

Zootaxa ◽  
2011 ◽  
Vol 3034 (1) ◽  
pp. 47 ◽  
Author(s):  
ADRIANO B. KURY ◽  
MIGUEL A. ALONSO-ZARAZAGA

Amendments are made to inconsistencies, mistakes and omissions in the catalogue of American Laniatores by Kury (2003). Discrepancies between dates given in Kury (2003) and Neave’s Nomenclator and the Zoological Record are discussed. Accurate issue dates for relevant publications are used to define priorities. Etymologies are surveyed for generic names, establishing their grammatical gender, so specific names are inflected according to the provisions of the Code. Unavailable generic names are: Messa Sørensen, 1932, Zarax Sørensen, 1932, Prasia Sørensen, 1932, Angistrisoma Roewer, 1932, Angistrisoma Mello-Leitão, 1935, Bunoweyhia Mello-Leitão, 1935, Batomites Mello-Leitão, 1931, Euminua Sørensen, 1932, Minua Sørensen, 1932, Ilhastygnus Roewer, 1943, Fonteboatus Roewer, 1931, Malea Sørensen, 1932, Chersobleptes Sørensen, 1932 and Jimeneziella Avram, 1970. Hernandria Banks, 1909 is unavailable and must be placed as an “incorrect subsequent spelling” of Hernandaria Sørensen, 1884. The valid genus name is Parahernandria Goodnight & Goodnight, 1947 (stat. res.). Zaraxolia Strand, 1942 (stat. res.) is revalidated from the synonymy of Neocynorta Roewer, 1915 with Zarax devians Sørensen, 1932 as type species. Friburgoia Mello-Leitão, 1932 [December] is deemed a junior subjective synonym of Schenkelibunus Strand, 1932 [September] (stat. res.) (inverted precedence between synonyms). Liops Mello-Leitão, 1940 (non Fieber, 1870, nec Gidley, 1906) is a junior homonym and is replaced by its first available synonym, Corcovadesia Soares & Soares, 1954 (stat. res.). The following unavailable generic names are formally described as new: (1) Jimeneziella Kury & Alonso-Zarazaga, gen. nov. (type species: Jimeneziella decui Avram, 1973); (2) Euminua Kury & Alonso-Zarazaga, gen. nov. (type species: Euminua brevitarsa Sørensen, 1932). The following homonym generic names are replaced: (1) Cranellus Roewer 1932, with Narcellus Kury & Alonso-Zarazaga, nom. nov., (2) Metapachylus Pickard-Cambridge, 1905, with Pyropharynx Kury & Alonso-Zarazaga, nom. nov.; (3) Ovalia González-Sponga, 1987, with Oo Kury & Alonso-Zarazaga, nom. nov.; (4) Tiara González-Sponga, 1987 with Mitraia Kury & Alonso-Zarazaga, nom. nov.; (5) Limonia González-Sponga, 1998, with Manuelangelia Kury & Alonso-Zarazaga, nom. nov. Gonyleptes melloleitaoi Kury & Alonso-Zarazaga, nom. nov. is a replacement name for Gonyleptes curvicornis Mello-Leitão, 1932. Discocyrtus confusus Kury, 2003 is unavailable, so this species is here re-described as Discocyrtus confusus Kury n. sp. New combinations are: Parahernandria spinosa (Banks, 1909) (from Hernandaria), Schenkelibunus impar (Mello-Leitão, 1932) (from Friburgoia), Schenkelibunus perditus (Mello-Leitão, 1927) (from Friburgoia), Narcellus balthazar (Roewer, 1932) (from Cranellus), Narcellus montgomeryi (Goodnight & Goodnight, 1947) (from Cranellus), Pyropharynx gracilis (Pickard-Cambridge, 1905) (from Metapachylus), Oo spinosum (GonzálezSponga, 1999) (from Ovalia), Mitraia unispina (González-Sponga, 1987) (from Tiara), Manuelangelia tuberosa (González-Sponga, 1998) (from Limonia), Zaraxolia devians (Sørensen, 1932) (from Zarax), Corcovadesia hexabunus (Mello-Leitão, 1940) (from Liops) and Corcovadesia venefica (H. Soares, 1966) (from Liops). The following genera of Pachylinae, which appeared in conflicting subfamilies in Kury 2003, are formally transferred to the Ampycinae: Ampycella Roewer, 1929, Glysterus Roewer, 1931, Hernandarioides Pickard-Cambridge, 1905, Parahernandria Goodnight & Goodnight, 1947 and Hutamaia Soares & Soares, 1977. A list of taxa described in 2003 is interpolated. A complementary list of the 2004–2009 systematic literature on the subject is given.

1993 ◽  
Vol 125 (S166) ◽  
pp. 3-85 ◽  
Author(s):  
J.M. Campbell

AbstractThe American species of the genera Bryoporus Kraatz and Bryophacis Reitter are revised for America north of Mexico. Two new related genera are described: Bolitopunctus (type species Bryoporus muricatulus Hatch) and Neobolitobius (type species Lordithon varians Hatch).The following new species are described: Bryoporus niger, Bolitopunctus punctatissimus, Bryophacis arcticus, Bryophacis canadensis, and Bryophacis smetanai. Six new combinations are created: Bolitopunctus muricatulus (Hatch) [from Bryoporus], Neobolitobius varians (Hatch) [from Lordithon], Bryophacis discalis (Hatch) [from Mycetoporus], Bry. punctatissimus (Hatch) [from Mycetoporus], Bry. punctulatus (Hatch) [from Mycetoporus], and Bry. rubescens (Hatch) [from Lordithon].Use of the generic names Bryoporus Kraatz and Bryophacis Reitter is discussed. Lectotypes are designated for Bryoporus rufescens LeConte and its junior synonyms B. rubidus LeConte and B. flavipes LeConte, and Bryoporus testaceus LeConte and its junior synonym B. parvulus Casey.All species of Bryoporus, Bryophacis, Bolitopunctus, and Neobolitobius are described and illustrated with line drawings and scanning electron photomicrographs. Keys are provided to distinguish all genera of North American Bolitobiini and all species of the genera treated in this revision. The New World distribution of each species treated is mapped. The biology of each species, if known, is discussed.


Zootaxa ◽  
2017 ◽  
Vol 4263 (1) ◽  
pp. 1 ◽  
Author(s):  
SAMUEL D. J. BROWN

The taxonomy of the New Zealand weevil genus Irenimus Pascoe, 1876 is revised, resulting in a narrower concept of the genus than has been considered in recent decades. In total, the genus now contains only seven species. In addition to the type species, I. parilis Pascoe, 1876, the genus contains I. duplex (Broun, 1904) and five newly described species: I. aniptus new species (type locality, Oamaru, DN), I. crinitus new species (type locality, Hakataramea Valley, SC), I. minimus new species (type locality, Alexandra, CO), I. stichus new species (type locality, Tekapo, MK) and I. thoracicus new species (type locality, Oamaru, DN). The genus Chalepistes new genus is established to contain the majority of species previously described in the genus Catoptes Schönherr, 1842, but also including species described in Brachyolus White, 1846; Irenimus Pascoe, 1876; Inophloeus Pascoe, 1875; and Nicaeana Pascoe, 1877. A total of 27 valid described species are new combinations with Chalepistes: C. aequalis (Broun, 1895) (from Irenimus), C. albosparsus (Broun, 1917) (from Irenimus), C. apicalis (Broun, 1923) (from Catoptes), C. asperatus (Broun, 1914) (from Brachyolus), C. compressus (Broun, 1880) (from Irenimus), C. costifer (Broun, 1886) (from Inophloeus), C. curvus (Barratt & Kuschel, 1996) (from Irenimus), C. dehiscens (Broun, 1917) (from Catoptes), C. dugdalei (Barratt & Kuschel, 1996) (from Irenimus), C. egens (Broun, 1904) (from Irenimus), C. inaequalis (Sharp, 1886) (from Brachyolus), C. instabilis (Marshall, 1931) (from Catoptes), C. latipennis (Broun, 1893) (from Catoptes), C. limbatus (Broun, 1909) (from Catoptes), C. lobatus (Broun, 1921) (from Catoptes), C. patricki (Barratt & Kuschel, 1996) (from Irenimus), C. pensus (Broun, 1914) (from Inophloeus), C. placidus (Broun, 1914) (from Nicaeana), C. posticalis (Broun, 1893) (from Irenimus), C. rhesus (Pascoe, 1875) (from Inophloeus), C. rubidus (Broun, 1881) (from Inophloeus), C. similis (Barratt & Kuschel, 1996) (from Irenimus), C. spectabilis (Broun, 1914) (from Catoptes), C. spermophilus (Broun, 1895), revised status (from Irenimus), C. stolidus (Broun, 1886) (from Irenimus), C. tenebricus (Broun, 1893) (from Catoptes), C. vastator (Broun, 1893) (from Irenimus). Numerous new synonyms with species of Chalepistes are also proposed: Brachyolus fuscipictus Broun, 1914 and Brachyolus terricola Broun, 1917 are junior subjective synonyms of Chalepistes asperatus (Broun); Brachyolus cervalis Broun, 1903 and Brachyolus sylvaticus Broun, 1910 are junior subjective synonyms of Chalepistes costifer (Broun); Inophloeus tricostatus Broun, 1915 is a junior subjective synonym of Chalepistes pensus (Broun); Catoptes pallidipes Broun, 1917, Catoptes flaviventris Broun, 1917 and Catoptes nigricans Broun, 1917 are junior subjective synonyms of Chalepistes placidus (Broun); Inophloeus longicornis Broun, 1904, Inophloeus medius Broun, 1893, Inophloeus sulcicollis Broun, 1914 and Inophloeus suturalis Broun, 1893 are junior subjective synonyms of Chalepistes rhesus (Pascoe); Inophloeus albonotata Broun, 1893, Catoptes asperellus Broun, 1893, Irenimus bicostatus Broun, 1886, Catoptes caliginosus Broun, 1893, Catoptes chalmeri Broun, 1893, Catoptes decorus Broun, 1893, Inophloeus discrepans Broun, 1904, Catoptes fumosus Broun, 1914, Catoptes furvus Broun, 1893, Catoptes humeralis Broun, 1893, Catoptes longulus Sharp, 1886, Inophloeus nigellus Broun, 1881, Irenimus pilosellus Broun, 1886 and Catoptes scutellaris Sharp, 1886 are junior subjective synonyms of Chalepistes rubidus (Broun); Catoptes subnitidus Broun, 1914 and Catoptes curvatus Broun, 1914 are junior subjective synonyms of Chalepistes spermophilus (Broun); Catoptes brevicornis Sharp, 1886 and Catoptes vexator Broun, 1904 are junior subjective synonyms of Chalepistes stolidus (Broun); and Catoptes aemulator Broun, 1893 and Catoptes argentalis Broun, 1914 are junior subjective synonyms of Chalepistes tenebricus (Broun). Additional new combinations include Inophloeus robustus (Broun, 1917) (from Catoptes) and Nicaeana fraudator (Marshall, 1931) (from Catoptes), while Catoptes postrectus Marshall, 1931 is a new synonym of Protolobus obscurus Sharp, 1886.


2019 ◽  
Vol 323 (Supplement 8) ◽  
pp. 1-594 ◽  

Hymenoptera is one of the largest insect orders, with a world fauna approximately of 160 thousand species in more than 8420 genera from 94 extant families, a Palaearctic fauna of 50–60 thousand estimated species, and a Russian fauna of 15.3 thousand species in 1999 genera from 78 families. The modern classification of Hymenoptera is given. The second volume treats the all recent groups of parasitoids (11 superfamilies, 43 families, 1466 genera, about 10.6 thousand species) recorded in the fauna of Russia. The sections for each of the 43 families include characteristics, number of taxa, references, and an annotated catalogue of the genera and species (subspecies) recorded from the fauna of Russia. For each valid genus, the type species, synonymy, short characterization, and number of species are given. For each valid species the synonymy, known host (often to genus or family level only) or sometimes host plants and distribution (in Russia and in general) are provided. The book is illustrated using geoschemes for Russia, Europe, and China. The large bibliography helps to assess the level of study of each family. The index of scientific names of Hymenoptera (more than 21 thousand names) will be useful for parasitoid taxa searching.


Zootaxa ◽  
2018 ◽  
Vol 4471 (1) ◽  
pp. 1
Author(s):  
JULIA J. MLYNAREK ◽  
TERRY A. WHEELER

The phylogenetic relationships of the chloropid tribe Elachipterini were analysed. Sixty-eight exemplar species and seven outgroup species were included in a cladistic analysis based on 76 morphological characters of adult specimens in order to test existing, non-phylogenetic, classifications of the tribe. Nine genera are recognized in the Elachipterini: Allomedeia Mlynarek & Wheeler, Alombus Becker, Anatrichus Loew, Ceratobarys Coquillett, Disciphus Becker, Elachiptera Macquart, Goniaspis Duda, Melanochaeta Bezzi and Sepsidoscinis Hendel. Myrmecosepsis Kertesz is synonymised with Anatrichus, and Togeciphus Nishijima and Cyrtomomyia Becker are synonymised with Elachiptera. Ceratobarys is removed from synonymy with Elachiptera and all Neotropical species and two Nearctic species previously assigned to Elachiptera are transferred to Ceratobarys. Melanochaeta is a valid genus; the type species Melanochaeta capreolus clusters with other species of Melanochaeta and not Oscinella. New combinations include Anatrichus hystrix (Kertesz, 1914) (Myrmecosepsis); Anatrichus taprobane (Andersson, 1977) (Myrmecosepsis), Ceratobarys attenuata (Adams, 1908) (Elachiptera); Ceratobarys cultrata (Wheeler & Forrest, 2002) (Elachiptera); Ceratobarys flavida (Williston, 1896) (Elachiptera); Ceratobarys melinifrons (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys fucosa (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys queposana (Mlynarek & Wheeler, 2008) (Elachiptera); Ceratobarys rubida (Becker, 1912) (Elachiptera); Ceratobarys sacculicornis (Enderlein, 1911) (Elachiptera); Ceratobarys willistoni (Sabrosky, 1948)  (Elachiptera), Elachiptera ensifer (Sabrosky, 1951) (Cyrtomomyia); Elachiptera ericius (Kanmiya, 1983) (Togeciphus); Elachiptera katoi (Nishijima, 1955) (Togeciphus); Elachiptera maculinervis (Becker, 1910) (Cyrtomomyia); Elachiptera punctulata (Becker, 1912) (Cyrtomomyia); Elachiptera subelongata (Kanmiya, 1983) (Disciphus); Elachiptera truncatus (Liu & Yang, 2012) (Togeciphus); Elachiptera tuberculata (Adams, 1905) (Cyrtomomyia) and all the species that were placed in Lasiochaeta are returned to Melanochaeta. A key to genera of the tribe Elachipterini is provided and diagnoses are provided for all genera. The tribe is divided into two geographically distinct clades: the Anatrichus clade includes the Old World tropical genera Allomedeia, Alombus, Anatrichus, Disciphus and Sepsidoscinis; the Elachiptera clade includes the primarily Neotropical genera Goniaspis and Ceratobarys and the widespread, but primarily Holarctic, genera Elachiptera and Melanochaeta. 


2017 ◽  
Vol 26 (2) ◽  
pp. 337-368 ◽  
Author(s):  
M. von Tschirnhaus

The taxonomic history for all species of a species-rich genus of the Chloropidae (Diptera) is briefly presented for the first time, by the example of the genus Elachiptera Macquart, 1835. Here, all names of the species-group ever combined with the generic name Elachiptera are listed together with the references and the first page of their descriptions, their first transfer into the valid genus, their senior and junior synonyms and further important references to their taxonomical status. In addition, all names of the genus group that have ever been associated with these species names are listed together with their type species. Thirty new combinations are introduced in order to transfer species from Melanochaeta Bezzi, 1906 (a synonym of Oscinella Becker, 1909) to the valid genera Lasiochaeta Corti, 1909 and Gampsocera Schiner, 1862. The known zoogeographical distribution of each of the 81 valid Elachiptera species and 74 valid species in other genera is briefly summarized. Selected exemplary data on larval habitats of Elachiptera are discussed.


1962 ◽  
Vol 40 (3) ◽  
pp. 447-490 ◽  
Author(s):  
Roy F. Cain

Podospora is the valid genus for a group of coprophilous species in which the ascospores have appendages but no gelatinous sheaths. The type species is P. fimicola Cesati. The following new species found on dung are described and illustrated: P. absimilis, Tautira; P. brasiliensis, Brazil; P. castorinospora, Panama Canal Zone; P. comatospora, Venezuela, Tautira, and Moorea; P. curvuloides, Brazil; P. inflatula, Tautira and Brazil; P. nannopodalis, New York; P. ostlingospora, Mexico; P. papilliformis, Venezuela and Mexico; P. prethopodalis, Tautira, Moorea, and Paea. The following are transferred from Pleurage as new combinations in Podospora: P. adelura (Griff.), P. anomala (Griff.), P. arizonensis (Griff.), P. collapsa (Griff.), P. gwynne-vaughaniae (Page), P. heterochaeta (Griff.), P. hyalopilosa (Stratton), P. immersa (Stratton), P. kansensis (Griff.), P. longicaudata (Griff.), P. taenioides (Griff.) and P. unicaudata (C. & M. Moreau). The following are transferred from Sordaria as new combinations in Podospora: P. araneosa (Cain), P. cervina (Cain), P. coronifera (Grove), P. curvispora (Cain), P. dubia (Hansen), P. eminens (Cain), P. fimbriate, (Bayer), P. globosa (Massee & Salmon), P. glutinans (Cain), P. inaequalis (Cain), P. inaequilateralis (Cain), P. kilimandscharica (A. Schmidt), P. leporina (Cain), P. linguiformis (Cain), P. ontariensis (Cain), P. perplexens (Cain), P. pilosa (Mouton), P. piriformis (Bayer), P. tetraspora (Winter). The following are transferred from Philocopra as new combinations in Podospora: P. coeruleotecta (Rehm) and P. millespora (A. Schmidt).


2000 ◽  
Vol 18 (1) ◽  
pp. 115-117
Author(s):  
Jan-Peter Frahm

The type species of Atractylocarpus has revealed to be a species of a genus which was later introduced as Camylopodiella. To avoid taxonomic confusions, it was proposed to keep the current use of Atractylocarpus and Campylopodiella by amending the genus Atractylocarpus. This proposal was rejected by the ICBN committee. Therefore the valid genus for all species so far comprised in Atractylocarpus is Metzleria and all species so far included in Campylopodiella must be transferred to Atractylocarpus. Accoringly, all necessary new combinations are introduced here: Atractylocarpus himalayanus (Broth.) J.-P. Frahm , Atractylocarpus malagensis (Herz.) J.-P. Frahm Metzleria comosa (Dix.) J.-P. Frahm, Metzleria madagascariensis (Thér.) J.-P. Frahm, Metzleria nana (Williams) J.-P. Frahm, Metzleria patagonica (Herz. et Thér.) J.-P. Frahm.


2017 ◽  
Vol 321 (Supplement 6) ◽  
pp. 1-475 ◽  

Hymenoptera is one of the largest insect orders, with a world fauna of 155.5 thousand species in 8423 genera from 94 extant families, a Palaearctic fauna of 50–60 thousand estimated species, and a Russian fauna of more than 15 thousand estimated species in more than 1500 genera from 78 families. The modern classification of Hymenoptera is given. The first volume treats the sawflies (13 families, 170 genera, 1546 species), wasps (15 families, 253 genera, 1695 species), ants (1 family, 44 genera, 264 species) and bees (6 families, 66 genera, 1216 species) which together, in Russia, comprise 4721 species in 533 genera. The sections for each of the 35 families include characteristics, number of taxa, references, and an annotated catalogue of the genera and species recorded from the fauna of Russia. For each valid genus the type species, synonymy, short characterization, and number of species are given. For each valid species the synonymy, known host plants, hosts or prey, and distribution (in Russia and general) are provided. The book is illustrated using geoschemes for Russia, Europe, and China. The large bibliography helps to assess the level of study of each family. The index of scientific names of Hymenoptera (more than 16000 names) will be useful for taxon searching.


Zootaxa ◽  
2003 ◽  
Vol 211 (1) ◽  
pp. 1 ◽  
Author(s):  
ARTHUR V. EVANS

A checklist and bibliography of the New World Melolonthinae are presented. As of 31 December 2002, the New World melolonthine fauna consists of 11 tribes, 122 genera, and 2,705 valid species, including 11 fossil species. The checklist is a synthesis of the tribal classifications of Blackwelder (1944), Britton (1978) and Evans (2002). Seven new combinations, eleven replacement names, and eight new synonymsare recognized. Thirteen varietal names were evalutated and determined to be subspecific in rank. The type species of 21 genera are here designated. Three genera and one species are listed as incertae sedis. Since the catalogs of Dalla Torre (1912, 1913) and Blackwelder (1944) two genera and two species have been removed from the New World Melolonthinae. Sericoides nossi Martínez, 1971 and Sericoides rechencqui Martínez, 1971 are nomina nuda.


1970 ◽  
Vol 102 (12) ◽  
pp. 1489-1507
Author(s):  
Eugene Munroe ◽  
Akira Mutuura

AbstractThe genus Placosaris Meyrick, type-species P. leucula Meyrick, Sangir, is redescribed. Xanthelectria Meyrick, type-species X. beatrix Meyrick of Java, is sunk as a subjective synonym of Placosaris. The following additional named species are referred to the genus as new combinations: Pyrausta cricophora West, Philippine Is.; Pyr. homoeides West, Philippine Is.; Pyr. triticalis Kenrick, New Guinea; Botys egerialis Snellen, Java, with Xanthelectria beatrix Meyrick as a new subjective synonym; Botys turiusalis Walker, Sarawak, with subjective synonyms B. eriggusalis Walker, Sarawak, B. broesialis Walker, Sarawak, and B. miniatalis Swinhoe, Sumatra; Opsibotys coorumba Hampson, Pyrausta auranticilialis Caradja, Canton; Pyr. subfuscalis Car.; Pachyzancla callistalis Hampson, Assam; Ebulea ochripunctalis Warren, Khasia Hills; Pachyzancla ustulalis Hampson, Ceylon; Ebulea intensalis Swinhoe, Khasia Hills; Psara tiawannalis Shibuya, Taiwan; Ps. intensalis rubellalis Caradja, Lienping, China; this last is considered specifically distinct from Placosaris intensalis. The following new species of Placosaris are described: P. steelei, Burma; P. swanni, Burma; P. lindgreni, Nagrispur; P. dohertyi, Assam; P. arjunoalis, Java and Bali; P. udealis, Assam; P. bornealis, Sarawak and Borneo; P. perakalis, Perak; P. apoialis, Mindanao; P. galogalis, Mindanao. Although the new species are mostly extralimital to Temperate East Asia, they are mostly related to Chinese species.


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