Revision of the genus Leptopilina Förster, 1869, with notes on the status of some other genera (Hymenoptera, Cynipoidea: Eucoitidae)

1980 ◽  
Vol 11 (4) ◽  
pp. 428-453 ◽  
Author(s):  
Göran Nordlander

AbstractThe genus Leptopilina Förster is revised on a world basis. The identity of 31 nominal species, including type species of four other genera, is discussed and 15 lectotypes are designated. Valid species of Leptopilina are L. longipes (Hartig) [type species], L. clavipes (Hartig) n. comb., L. heterotoma (Thomson) n. comb., L. fimbriata (Kieffer) n. comb., L. rufipes (Cameron) n. comb., L. atraticeps (Kieffer) n. comb., L. mahensis (Kieffer) n. comb., L. boulardi (Barbotin et al.) n. comb., and L. cupulifera (Kieffer) n. comb. Leptopilina heterotoma is the valid name for the well-known Drosophila parasitoid currently referred to as Pseudeucoila bochei (Weld). Leptopilina is not synonymous with Ganaspis Förster. Tryhliographa Förster is a senior synonym of Episoclu Förster n. syn. and of Pseudeucoila Ashmead (synonymy confirmed). Leptopilina is described and compared with related genera (Cothonaspis, Rhoptromeris, Odonteucoila). L. victoriae n. sp. is described from the Seychelles. The five Leptopilina occurring in Europe are redescribed on modern material and a key is given to them.

Zootaxa ◽  
2007 ◽  
Vol 1418 (1) ◽  
pp. 1-628 ◽  
Author(s):  
CARL J. FERRARIS

A checklist of Recent and fossil catfishes (Order Siluriformes) is presented, summarizing taxonomic literature published through 2005. From 4624 nominal species group names and 810 genus group names, 3093 species are recognized as valid, and are distributed among 478 genera and 36 families. Distributional summaries are provided for each species, and nomenclatural synonymies, including relevant information on all name-bearing types, are included for all taxa. One new name is proposed herein: Clariallabes teugelsi, as a replacement for Clarias (Allabenchelys) dumerili longibarbis David & Poll, 1937, which is preoccupied by Clarias longibarbis Worthington, 1933, but has been treated as a valid species of Clariallabes by Teugels. Acrochordonichthys melanogaster Bleeker, 1854, is designated as type species of Acrochordonichthys Bleeker, 1857, inasmuch as no earlier valid designation has been found. A new genus Pseudobagarius, is proposed for the “pseudobagarius group” of species formerly placed in Akysis. The status of 228 species group names remains unresolved and 31 names based on otoliths ascribed to catfishes are listed but not placed into the checklist. The current emphasis given to catfish taxonomy at present is likely to result in a dramatic increase in the total number of valid taxa as well as major changes in the membership of some of the higher level taxa recognized here.


2012 ◽  
Vol 144 (1) ◽  
pp. 169-181 ◽  
Author(s):  
Thomas Pape ◽  
Krzysztof Szpila

AbstractThe nominal taxon Tachina macularis Wiedemann is revised and redescribed from the adult and first instar larva. It is transferred from its current status as a valid species of Protomiltogramma Townsend to a position as a valid species of Eremasiomyia Rohdendorf, comb. nov. and senior synonym of Setulia luteicornis Villeneuve, syn. nov., Eremasiomyia setulioides Rohdendorf, syn. nov., and Eremasiomyia orientalis Verves, syn. nov. The nominal species Sphecapatodes maroccana Séguy is revised and redescribed from the adult, and is shown to belong to Miltogramma Meigen, comb. nov. The nominal genus-group taxon Capnopteron Rohdendorf was originally proposed as a subgenus of Miltogramma with the type species Miltogramma maculigerum Speiser sensu Rohdendorf). However, the latter is shown to be a misidentification of Miltogramma maroccana (Séguy), which herewith is fixed as the type species of Capnopteron.


1991 ◽  
Vol 123 (S160) ◽  
pp. 3-341 ◽  
Author(s):  
Jean-François Landry

AbstractGenera and previously described species of Nearctic Scythrididae are revised for the first time, based on the study of adult structures. About 90 percent of the Nearctic fauna known in collections consists of undescribed species. The supraspecific taxa treated in this work encompass less than half of the Nearctic species diversity. Only six new species are described, all within the largest and structurally most diverse genus. The status of all nominal species is revised. Valid species are redescribed and their features illustrated. General problems in the systematics of the Scythrididae are discussed. A description of adult features of the family Scythrididae is providad. Extra-limital genera are briefly reviewed. A key to the Nearctic genera and informal supraspecific lineages is provided.Six genera, including three new, are treated: Areniscythris Powell, 1976, Arotrura Walsingham, 1888, Asymmetrura gen. nov., Neoscythris gen. nov., Rhamphura gen. nov., and Scythris s. str. Hübner, [1825]. Areniscythris includes a single described species, Areniscythris brachypteris Powell, but is defined more broadly to account for a number of undescribed species. Arotrura is divided into nine informal species groups with the following included species: Arotrura atascosa sp. nov., Arotrura balli sp. nov., Arotrura divaricata (Braun) comb, nov., Arotrura eburnea Walsingham, Arotrura formidabilis sp. nov., Arotrura hymenata sp. nov., Arotrura longissima sp. nov., Arotrura oxyplecta (Meyrick) comb, nov., Arotrura powelli sp. nov., and Arotrura sponsella (Busck) comb. nov. Asymmetrura includes: Asymmetrura albilineata (Walsingham) comb. nov., Asymmetrura graminivorella (Braun) comb. nov., Asymmetrura impositella (Zeller) comb. nov. and type species, Asymmetrura matutella (Clemens) comb, nov., Asymmetrura reducta (Braun) comb, nov., and Asymmetrura scintillifera (Braun) comb. nov. Neoscythris includes: Neoscythris confinis (Braun) comb, nov., Neoscythris euthia (Walsingham) comb. nov., Neoscythris fissirostris (Meyrick) comb. nov. and type species, and Neoscythris planipenella (Chambers) comb. nov. Rhamphura includes: Rhamphura altisierrae (Keifer) comb, nov., Rhamphura ochristriata (Walsingham) comb. nov. and type species, Rhamphura perspicillella (Walsingham) comb. nov., Rhamphura suffusa (Walsingham) comb. nov., and the extra-limital Rhamphura immunis (Meyrick) comb. nov. from Peru. Scythris s. str. includes: Scythris immaculatella (Chambers) rev. stat., Scythris limbella (Fabricius), Scythris mixaula Meyrick, Scythris trivinctella (Zeller), and Scythris ypsilon Braun. A further eight species are phylogenetically distinct from Scythris s. str. but provisionally are only assigned to five informal monophyletic lineages until their cladistic relationships are more firmly established. These are: the Scythris basilaris lineage including Scythris basilaris (Zeller), Scythris eboracensis (Zeller), and Scythris fuscicomella (Clemens); the Scythris interrupta lineage including Scythris interrupta Braun; the Scythris inspersella lineage including Scythris inspersella (Hübner) and Scythris noricella (Zeller); the Scythris anthracina lineage including Scythris anthracina Braun; and the Scythris charon lineage including Scythris charon Meyrick. Three species are incertae sedis: Scythris inornatella (Chambers) comb, nov., Scythrispilosella (Zeller), and Scythris piratica Meyrick.Coleophora albacostella Chambers and Coleophora inornatella Chambers are transferred from the Coleophoridae. Scythris arizoniella (Kearfott) is transferred to the Coleophoridae [Coleophora arizoniella (Kearfott) comb. nov.].The following new synonymy is proposed: Colinita Busck, 1907 = Arotrura Walsingham, 1888; Gelechia aterrimella Walker, 1864 and Scythris epilobiella McDunnough, 1942 = Scythris inspersella [Hübner, (1817)]; Scythris magnatella Busck, 1904 = Scythris noricella (Zeller, 1843); Scythris pacifica McDunnough, 1927 = Scythris immaculatella (Chambers, 1875); Coleophora albacostella Chambers, 1875 and Scythris hemidictyas Meyrick, 1928 = Neoscythris planipenella (Chambers, 1875).A cladistic definition of the family is presented for the first time. The monophyly of the Scythrididae is supported by the following synapomorphies: very narrow ductus bursae, broad ductus seminalis anastomosed with the oviduct and the corpus bursae, lack of signum, unique shape of the apophyses of the metathoracic furca, tarsomeres 1–4 with two subapical spurs, aedeagus ankylosed, and origin of forewing veins R4 and R5 on a common stalk with R4 extended to the costa and R5 to the termen. Relationships of the Scythrididae within the Gelechioidea are discussed. Based on the cladistic analysis of 52 structural characters, phylogenetic relationships of supraspecific taxa are inferred. Two cladograms, one for the genera and one for the species groups of Arotrura, are presented and used in deriving the classification.


Zootaxa ◽  
2019 ◽  
Vol 4685 (1) ◽  
pp. 1-67 ◽  
Author(s):  
IRENE LOBATO-VILA ◽  
JULI PUJADE-VILLAR

A taxonomic revision of the tribe Ceroptresini (Hymenoptera: Cynipidae) is conducted for the first time. Prior to this study, the total number of valid species of Ceroptres, the only genus within Ceroptresini to date, was 23. As a result of this revision, 15 Ceroptres species are retained as valid and one species, Amblynotus ensiger Walsh, 1864, is desynonymized from Ceroptres petiolicola (Osten-Sacken, 1861), being considered here as a valid Ceroptres species: C. ensiger (Walsh, 1864) status verified and comb. nov. An additional five new species are described from Mexico: Ceroptres junquerasi Lobato-Vila & Pujade-Villar sp. nov.; C. lenis Lobato-Vila & Pujade-Villar sp. nov.; C. mexicanus Lobato-Vila & Pujade-Villar sp. nov.; C. nigricrus Lobato-Vila & Pujade-Villar sp. nov.; C. quadratifacies Lobato-Vila & Pujade-Villar sp. nov., increasing the total number of valid Ceroptres species to 21. Ceroptres masudai Abe, 1997 is synonymized with C. kovalevi Belizin, 1973. Ceroptres niger Fullaway, 1911 is transferred to Andricus (Andricus confusus Lobato-Vila & Pujade-Villar comb. nov. and nom. nov.). Five species (Amblynotus inermis Walsh, 1864; Cynips quercusarbos Fitch, 1859; Cynips querficus Fitch, 1859; Cynips quercuspisum Fitch, 1859; and Cynips quercustuber Fitch, 1859) are not considered as valid Ceroptres. The status of Ceroptres quereicola (Shinji, 1938), previously classified as an unplaced species, is commented on. In addition, a Nearctic species from the USA, Ceroptres politus Ashmead, 1896, is here proposed as the type species of a new genus within Ceroptresini: Buffingtonella Lobato-Vila & Pujade-Villar gen. nov. Redescriptions, biological and distribution data, illustrations and keys to genera and species within Ceroptresini are provided. The diagnostic morphological traits of Ceroptresini, Ceroptres and the new genus are discussed. 


Zootaxa ◽  
2011 ◽  
Vol 2992 (1) ◽  
pp. 1-51
Author(s):  
PATRICK DAVID ◽  
GERNOT VOGEL ◽  
ALAIN DUBOIS

This paper analyzes the consequences of the non-respect of the Rules of the Code to ascertain the valid subsequent designation of the nucleospecies (type species) of the nominal genus Trimeresurus Lacépède, 1804. The long accepted designation was invalid because it was based on a nominal species which was not among the prenucleospecies (originally included species) of the nominal genus. In contrast with the commonly accepted viewpoint which makes the Indian taxon Coluber gramineus Shaw, 1802 the nucleospecies of the genus, we show that this role is played by Trimeresurus viridis Lacépède, 1804, a species inhabiting the Lesser Sunda Islands and Timor and, as a nomen oblitum, a senior synonym of Trimeresurus albolabris insularis Kramer, 1977, a taxon now considered a distinct species. The important nomenclatural implications of this finding are discussed here, especially with regard to the recent splitting of the genus Trimeresurus. The generic nomen Trimeresurus should be associated with the Trimeresurus albolabris group of species currently placed in the genus or subgenus Cryptelytrops Cope, 1860. A lectophoront (lectotype) is selected and described for Trimeresurus viridis Lacépède, 1804. Coluber viridis Bechstein, 1802 is an invalid objective junior synonym of Coluber gramineus Shaw, 1802. The current content of the genus Trimeresurus and of its eight subgenera is provided. Some clarifications or improvements to the Code are suggested.


2019 ◽  
Vol 39 ◽  
pp. 39-76 ◽  
Author(s):  
Hiroshi Kajihara

The taxonomic identity of the palaeonemertean Cephalothrix linearis (Rathke, 1799) has been obscure for nearly two centuries, because its original description applies to almost any congeners, including Cephalothrix filiformis (Johnston 1828) and Cephalothrix rufifrons (Johnston, 1837), which occur commonly in the North Sea and adjacent waters. In this paper, I redescribe C. linearis based on two topotypes from Bergen, one herein designated as the neotype for C. linearis, because Rathke’s original material is not extant; I invoke Article 70.3.2 of the International Code of Zoological Nomenclature to fix Planaria linearis Rathke, 1799 as the type species of Cephalothrix Örsted, 1843 for the sake of stability. From the neotype, I determined sequences of the 28S rRNA, 16S rRNA, and cytochrome c oxidase subunit I (COI) genes. Using the COI sequence, I inferred the phylogenetic position of C. linearis along with 316 cephalotrichid sequences currently available in public databases. A tree-based species delimitation analysis detected 43 entities among them, with 34 in Cephalothrix and nine in eitherBalionemertes or Cephalotrichella. I apply valid species names to 12 of the 34 entities in Cephalothrix. I tabulated a total of 36 nominal species that are likely the members of the genus; the following five were excluded even though their specific names were originally combined with Cephalothrix: Cephalothrix armata Ulyanin, 1870 [Monostilifera, possibly Emplectonema gracile (Johnston, 1837)], Cephalothrix fragilis Bürger, 1892 [now Cephalotrichella signata (Hubrecht, 1879)], Cephalothrix signata Hubrecht, 1879 [now in Cephalotrichella], Cephalothrix unipunctata Parfitt, 1867 [now Tetrastemma melanocephalum (Johnston, 1837) (Monostilifera)], and Cephalothrix viridis Chapuis, 1886 [possibly Heteronemertea]. The five names cephalothrix Diesing, 1850 (as Borlasia cephalothrix), kroyeri Diesing, 1850 (as Cephalothrix kroyeri), linearis Diesing, 1850 (as Borlasia linearis), lineata Claparède, 1862 (as Cephalothrix lineata), and oerstedii Diesing, 1850 (as Cephalothrix oerstedii) aredeclared nomenclaturally unavailable.


Zootaxa ◽  
2007 ◽  
Vol 1627 (1) ◽  
pp. 1-22 ◽  
Author(s):  
CARLOS J.A. CAMPOS ◽  
ANTONIO C. MARQUES ◽  
ALVARO E. MIGOTTO

The hydrozoan genus Zyzzyzus is revised based on reexaminations of all available type specimens and on additional material. The taxon includes four valid species: Zyzzyzus spongicolus (von Lendenfeld, 1884), from the eastern Indian and southwest Pacific oceans; the type species, Z. warreni Calder, 1988, from the Atlantic, western Indian, and western Pacific oceans; and Z. floridanus Petersen, 1990 and Z. robustus Petersen, 1990, both from the northwest Atlantic. Although type specimens of Z. calderi Petersen, 1990 could not be located, it has been assigned here to the synonymy of Z. warreni because of similarities between the two in nematocyst dimensions, in number and structure of endodermal canals, and in external morphology of the hydrocaulus and hydrorhiza. A sixth nominal species (Corymorpha iyoensis Yamada, 1958) has on one occasion been assigned to the genus, but detailed studies of the type material are needed to resolve its taxonomic affinities.


Bionomina ◽  
2021 ◽  
Vol 21 (1) ◽  
pp. 123-139
Author(s):  
DIETRICH KADOLSKY

Nomenclatural issues pertaining to selected non-marine gastropods of Cretaceous and Tertiary age are discussed and resolved as follows. [1] Viviparus hammeri (Defrance, 1825) is reinstated; Helicites viviparoides Schlotheim, 1820 is a nomen nudum, made available as Paludina viviparoides Bronn, 1848, a new objective synonym. [2] Viviparus frauenfeldi Le Renard, 1994 is a new objective synonym of Viviparus oulchyensis Wenz, 1919. [3] Lorus is proposed as a nomen novum for Liris Conrad, 1871 [nec Fabricius, 1804]. [3] Wesselinghia is proposed as a nomen novum for Longosoma Wesselingh & Kadolsky, 2006 [nec Hartman, 1944]. [4] Hydrobia incerta (Deshayes, 1862) is reinstated; Hydrobia antoni Le Renard, 1994 is a new objective synonym of this nomen. [5] The species Paludina frauenfeldi Hoernes, 1856 is designated as type species of Sarmata B. Dybowski & Grochmalicki, 1920. [6] The misidentified type species of Annulifer Cossmann, 1921, so far known as ‘Paludina protracta sensu Cossmann 1921, non Eichwald, 1850’, is fixed under Article 70.3 of the Code as understood by Cossmann (1921), and renamed Annulifer annulifer new species. [7] Pomatias turgidulus (Sandberger, 1872) is reinstated; P. turonicus Wenz, 1923 and Cyclostoma squamosum Peyrot, 1932 are its new objective synonyms. [8] Valvata inflata Sandberger, 1875 is reinstated; V. gaudryana Wenz, 1928 [nec Mortillet, 1863] is its new objective synonym. [8] Catinella? montana Pierce, new species, originally published as “[Succineidae] montana Pierce, 1992”, is made available by associating the species epithet with a generic nomen. [9] Proalbinaria subantiqua (d’Orbigny, 1850) is reinstated; its senior synonym Pupa antiqua Matheron, 1832 is a primary junior homonym of Pupa muscorum antiqua Eichwald, 1830. [10] The type species of Palaeostoa Andreae, 1884 is Pupa fontenayi Sandberger, 1871 by subsequent designation by Cossmann (1905), which has precedence over the designation of Clausilia crenata Sandberger, 1871 by Wenz (1923). [11] Palaeostoa elongata (Melleville, 1843), whose original combination was Pupa elongata, is a primary junior homonym of Pupa elongata Bouillet, 1836, an unused name for an unidentified nominal species; pending more information on the taxon at stake, maintenance of the existing usage is recommended. [12] Scalaxis columnella (Deshayes, 1863) is reinstated, with Scalaxis sinister Wenz, 1923 as its new synonym. [13] Eurystrophe olla (Serres, 1844) is reinstated, with Helix janthinoides Noulet, 1868 [nec Helix janthinoides Serres, 1829, a nomen nudum] as its new synonym.


2005 ◽  
Vol 19 (6) ◽  
pp. 557 ◽  
Author(s):  
Cinthya S. G. Santos ◽  
Fredrik Pleijel ◽  
Paulo Lana ◽  
Greg W. Rouse

Nereididae Johnston, 1865, part of the large clade Phyllodocida, is one of the best-known annelid groups. Presently, there are some 500 nominal species grouped into 42 genera, although there is little consensus among different authors as to how they should be classified. The relationships of nereidids were assessed in a morphology-based parsimony analysis of 41 terminal taxa, with members of Chrysopetalidae and Hesionidae used as outgroups. Type species for the majority of currently recognised nereidid genera were used as terminal taxa, and character information was based on examination of type and non-type specimens, together with literature descriptions. High degrees of homoplasy were found for several features that are traditionally applied to delineate subgroups of Nereididae, including the presence of paragnaths and the distribution of different kinds of chaetae. Six major groups were recovered: Namanereidinae, including Namalycastis and Namanereis, characterised by spherical shape of palpostyles and ventrally displaced notoaciculae; one clade corresponding in part to previous authors concepts of Nereidinae, including Nereis, Eunereis, Hediste and Platynereis (the relationships of several well known nereidids, such as Neanthes and Perinereis, commonly referred to Nereidinae, could not be unambiguously resolved); one unnamed and not previously recognised clade (A), including Australonereis, Laeonereis, Dendronereides and Olganereis, characterised by the presence of papillae on the maxillary ring; a second unnamed clade (B), including Leptonereis, Sinonereis, Tylonereis and Tylorrhynchus, characterised by enlarged notopodial ligulae; a well supported Gymnonereidinae, restricted to Ceratocephale, Gymnonereis, Tambalagamia and Micronereides; and a third unnamed clade (C), including Ceratonereis, Solomononereis, Unanereis, Cheilonereis and Websterinereis, characterised by unilobated neuropodial postchaetal lobes. Among these groups we found good support for the Namanereidinae, the Gymnonereidinae and for the whole of Nereididae. The subfamilies Dendronereidinae and Notophycinae (based on Micronereis, senior synonym of Notophycus) are regarded here as monotypic.


Zootaxa ◽  
2019 ◽  
Vol 4706 (2) ◽  
pp. 255-274 ◽  
Author(s):  
FELISTA KASYOKA KILUNDA ◽  
WERNER CONRADIE ◽  
DOMNICK VICTOR WASONGA ◽  
JIE-QIONG JIN ◽  
MIN-SHENG PENG ◽  
...  

Historically Panaspis wahlbergi (Smith, 1849) has been the only assignable species present in Kenya. Recent studies have shown that it comprises multiple cryptic species and the nominal species is now restricted to southern Africa. Newly collected mitochondrial data (16S rRNA) helped to resolve the status of the Kenyan populations, which revealed the presence of two distant related species. Pairwise distances show average 5.87% differences between the two Kenyan species, and 3.58–5.27% and 8.62–9.15% to nominal P. wahlbergi and P. maculicollis Jacobsen & Broadley, 2000 respectively. Ablepharus massaiensis Angel, 1924 was described from the Maasai plains near Nairobi, but has long been considered a junior synonym of P. wahlbergi. We herein resurrect Panaspis massaiensis comb. nov. as a valid species and describe a new species, Panaspis tsavoensis sp. nov. from the Tsavo Conservation Area in south-eastern Kenya. Morphological examinations of specimens reveal minor differences from each other as well as nominal forms of P. wahlbergi and P. maculicollis. Panaspis massaiensis comb. nov. shares with the P. wahlbergi group a white ventrolateral stripe but can be distinguished by the presence of 26 midbody scale rows versus 24. Panaspis tsavoensis sp. nov. on the other hand, lacks the white ventrolateral stripe, most similar to the P. maculicollis group but differs in that P. maculicollis breeding males have a black patch on the neck with diagonal rows of white spots. Panaspis massaiensis comb. nov. is widespread in the Kenyan and northern Tanzanian highlands, isolated dryland montane forests and rocky hills, while P. tsavoensis sp. nov. occur in the expansive arid lowlands of Tsavo Conservation Area and should be present in similar arid lowlands in northern Kenya as well as in adjacent Tanzania. 


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