scholarly journals A revision ofHaematodesLaporte andWeiserianumBernhauer (Coleoptera: Staphylinidae: Staphylininae: Xanthopygina)

PeerJ ◽  
2018 ◽  
Vol 6 ◽  
pp. e4582 ◽  
Author(s):  
Adam J. Brunke ◽  
Stylianos Chatzimanolis

The species of poorly known but charismatic generaHaematodesLaporte, 1835 andWeiserianumBernhauer, 1927 are revised.Weiserianumsyn. nov.is considered a junior synonym ofHaematodes, withHaematodes kuntzeni(Scheerpeltz, 1936)comb. nov.Weiserianum woltersiBernhauer, 1927syn. nov.is treated as a synonym ofHaematodes tenuipesKraatz, 1858.Haematodes myterossp. nov., is described from Paraguay and Brazil. As the type series ofHaematodes bicolorLaporte, 1835 is considered lost, a neotype, selected from the original type locality is designated. We also designate a lectotype forH. tenuipesKraatz, 1858 to stabilize nomenclature for this species, which is similar toH. myteros. As far as known,Haematodesis restricted to the southern Neotropical region and may be nest parasites withinAcromyrmexandAttaant nests as are species of the related genusScariphaeus, but no direct observations are yet available. We provide a key to the four known species ofHaematodesand illustrate their diagnostic features.

2020 ◽  
Vol 29 (1) ◽  
pp. 33-57
Author(s):  
V.M. Loskot ◽  
G.B. Bakhtadze

Geographic distribution and habitat preferences of Saxicola rubicola rubicola (Linnaeus, 1766), S. maurus variegatus (S.G. Gmelin, 1774), and S. m. armenicus (Stegman, 1935) inhabiting the Caucasian Isthmus and adjacent areas are described in detail. We examined the individual, sexual, age, seasonal and geographical variations of seven main diagnostic features of both plumage and morphometrics (exactly, the length of wing and tail) using 381 skin specimens. Substantially improved diagnoses of S. m. variegatus and S. m. armenicus are provided. After a thorough examination of the materials and history of the expedition of Samuel Gmelin in 1768–1774, and his description of Parus variegatus, it was concluded that the type locality of this taxon was the vicinity of Shamakhi in Azerbaijan not Enzeli in North-Western Turkey. It is also shown the fallacy of the recently proposed attribution of the holotype of the northern subspecies S. m. variegatus to the southern taxon S. m. armenicus and synonymisation of these names, as well as the replacement of the name S. m. variegatus by its junior synonym S. m. hemrichii Ehrenberg, 1833 for the northern subspecies.


2012 ◽  
Vol 35 (1) ◽  
pp. 99-106
Author(s):  
A. Martínez-Ortí ◽  
◽  
F. Robles ◽  

To determine the taxonomic identity of some of the species included in the genus Iberus, we reviewed the type series described by Rossmässler (1854) and deposited at the Senckenberg Forschungsinstitut und Naturmuseum of Frankfurt (Germany). We concluded that Helix alcarazana (currently Iberus alcarazanus) is a junior synonym of Iberus alonensis (Férussac, 1821). The type localities of Helix guiraoana and Helix alcarazana were discussed and modified and the lectotypes of Helix guiraoana, Helix guiraoana var. angustata, Helix alcarazana and Helix loxana were designated. In addition, we reviewed the type series of Helix alonensis Férussac, 1821 (currently Iberus alonensis) deposited at the Muséum national d’Histoire naturelle of Paris, France and we selected its lectotype. The locality of Alicante has been designated as the restricted type locality of this species.


Zootaxa ◽  
2007 ◽  
Vol 1554 (1) ◽  
pp. 67-68
Author(s):  
BRADLEY J. SINCLAIR

During the latter stages of revisionary work on the genus Clinocera Meigen (Sinclair in prep.), the type series of most species were examined. In an earlier paper Sinclair (1999) compared European and North American types of the C. appendiculata group, which resulted in several redefinitions and synonyms. In this short correspondence, the results of an examination of a series of specimens from the original type series of C. rufipes Bezzi and the remaining syntype of C. nigra Meigen are also reported


Zootaxa ◽  
2009 ◽  
Vol 2112 (1) ◽  
pp. 65-67
Author(s):  
SCOTT E. BROOKS ◽  
JEFFREY M. CUMMING

Thambemyia Oldroyd is a marine shore dolichopodid genus in the aphrosyline subgroup of the subfamily Hydrophorinae. The genus was erected by Oldroyd (1956) based on the greatly elongated proboscis of the Malaysian species T. pagdeni Oldroyd. Since the early 1980’s the generic limits of Thambemyia have been in flux as a result of differing opinions regarding the proposed synonymy of the related genus Conchopus Takagi, 1965 by Meuffels & Grootaert (1984). Masunaga et al. (2005) argued to retain the generic status of Conchopus in a much restricted sense (i.e., the rectus species group of Takagi), but did not provide evidence to support that classification, however later Masunaga in Zhu et al. (2005) appears to have reversed this decision. Recent catalogs have all treated Conchopus as a junior synonym of Thambemyia (Bickel & Dyte 1989; Pollet et al. 2004; Yang et al. 2006). Presently Thambemyia (sensu Meuffels & Grootaert 1984) includes 24 described species from Japan, China and the Hawaiian Islands (Yang et al. 2006). Masunaga & Saigusa (2006) reported an additional five undescribed species (as Conchopus) from the Hawaiian Islands.


2015 ◽  
Vol 147 (6) ◽  
pp. 665-673 ◽  
Author(s):  
Eduardo M. Shimbori ◽  
Scott R. Shaw ◽  
Angélica M. Penteado-Dias

AbstractSpecies of theAleiodes compressor(Herrich-Schaeffer) species group (Hymenoptera: Braconidae: Rogadinae) from the New World are revised. Two new species are described (Aleiodes mantiqueirensisnew speciesandAleiodes marinoniinew species) and geographical range of the species group is extended into the Neotropical Region. Both new species are known only from the type locality in Brazil. Including the current descriptions, there are six species within theAleiodes compressorspecies group, four of them from the New World. Some new diagnostic characters for the group are proposed such as the relative length of antenna and the shape of ovipositor sheaths. The males of this group are difficult to distinguish from males of theAleiodes gastritor-circumscriptusspecies group because most diagnostic features are found only in females.


1992 ◽  
Vol 23 (3) ◽  
pp. 249-273 ◽  
Author(s):  
C.A. Viraktamath

AbstractThe type series of 18 out of 19 species of Nirvaninae described by C. F. Baker in nine genera were examined and lectotypes designated. Jassonirvana lineata Baker and Stenometopius mindanaoensis Baker are removed from the Nirvaninae as they belong to Deltocephalinae. Each of the remaining species and Kana maculata Baker (based on specimen collected from the type locality) are redescribed with respect to the male and female genitalia wherever available and are illustrated. Keys to included genera and species are also provided. Pseudonirvana Baker is treated as a junior synonym of Sophonia Walker. New combinations proposed are Sophonia marginata (Baker) (from Ophiuchus), Pactana picea (Baker) (from Kana), Nirvana sanguinolineata (Baker) and Nirvana davaoensis (Baker) (both from Pseudonirvana). The latter species is treated as a junior synonym of Nirvana philippinensis Baker. The genera Nirvanoides Baker, Pythonirvana Baker and Pactana Linnavuori are redescribed.


Zootaxa ◽  
2011 ◽  
Vol 2900 (1) ◽  
pp. 51 ◽  
Author(s):  
DAN A. POLHEMUS

New distribution records are provided for the following 16 taxa of Gyrinidae on New Guinea, some of which have not been documented since their original type series were collected in the late 1800s or early 1900s: Porrorhynchus (Rhomborhynchus) depressus depressus Régimbart; Porrorhynchus (Rhomborhynchus) depressus misoolensis Ochs new combination; Dineutus (Rhombodineutus) pectoralis pectoralis Régimbart; Dineutus (Rhombodineutus) pectoralis biakensis Brinck; Dineutus (Rhombodineutus) pectoralis monticola Ochs; Dineutus (Rhombodineutus) heurni Zimmerman; Dineutus (Rhombodineutus) silenus Brinck; Dineutus (Rhombodineutus) sinuaticollis Zimmerman; Dineutus (Rhombodineutus) virescens Ochs; Dineutus (Rhombodineutus) chalybeus Zimmerman; Dineutus (Rhombodineutus) helleri stueberi Ochs; Dineutus (Rhombodineutus) tetracanthus tetracanthus Régimbart; Dineutus (Merodineutus) archboldianus Ochs; Dineutus (Merodineutus) loriae Régimbart; Dineutus (Merodineutus) macrochirus Régimbart; and Dineutus (Spinosodineutes) neohollandicus Ochs. New distribution records are also provided for Dineutus (Dineutus) regimbarti regimbarti Régimbart from East Timor. The type-locality of Dineutus (Rhombodineutus) chalybeus is constrained to Yule Island, on the Gulf of Papua. Updated distribution maps are provided for all the New Guinea species above, a table is included summarizing currently documented ranges of elevation and water temperature for all species treated, and a checklist of all species of Gyrinidae currently known from New Guinea and nearby islands is provided, with species assigned to putative areas of freshwater endemism within the island.


Zootaxa ◽  
2019 ◽  
Vol 4560 (3) ◽  
pp. 554 ◽  
Author(s):  
RENATA STOPIGLIA ◽  
ALAIN DUBOIS ◽  
FLÁVIO A. BOCKMANN ◽  
MARCOS A. RAPOSO

Different authors have suggested that Anabates pulvericolor Sclater, 1858 might be the valid nomen for Synallaxis propinqua Pelzeln, 1859 or for Synallaxis gujanensis huallagae Cory, 1919. However, due to doubts regarding the taxonomic identity of Anabates pulvericolor Sclater, 1858, of which the unique type is lost, neither of these nomina has been displaced by the senior nomen pulvericolor. Our analysis of the case reveals that Anabates pulvericolor Sclater, 1858 is correctly identifiable with Synallaxis gujanensis huallagae Cory, 1919, of which it is a senior subjective synonym. According to the Code, the senior subjective synonym Synallaxis gujanensis pulvericolor (Sclater, 1858) should be adopted. Given the fact that the holotype of Anabates pulvericolor Sclater, 1858 is missing and that it has been impossible to identify it from its description until now, we designate a neotype from“Río Napo, Ecuador”, its original type locality. 


Zootaxa ◽  
2020 ◽  
Vol 4750 (3) ◽  
pp. 432-436
Author(s):  
ROMAIN JATTIOT ◽  
BENJAMIN LATUTRIE ◽  
ANDRÉ NEL

The discovery of the first damselfly Lestes regina Théobald, 1937 from Monteils (Gard, France) supports the identity of late Eocene age of this outcrop with the historical outcrop of Célas, type locality for the type series of this species. Lestes regina is also documented from the late Eocene Isle of Wight basin, confirming the presence of significant contacts between this southern area and the anglo-Parisian lacustrine basin at that time. Nearly all the Eocene and Oligocene fossil Lestes from Western Europe have a particular character, viz. the presence of a supplementary row of cells between the veins MP and CuA. This character is much less frequent in extant Lestes and is still unknown among Neogene representatives of the genus. 


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. 


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