scholarly journals On the taxonomical identity of some taxa of the Iberian endemic genus Iberus Montfort, 1810 (Gastropoda, Helicidae)

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.

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.


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.


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.


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. 


PeerJ ◽  
2021 ◽  
Vol 9 ◽  
pp. e11682
Author(s):  
Caio Gueratto ◽  
Alípio Benedetti ◽  
Ricardo Pinto-da-Rocha

The type species of Mischonyx Bertkau 1880, Mischonyx squalidus, was described based on a juvenile. The holotype is lost. Based on a revision of publications, the genus includes 12 species, all in Brazil. The objectives of this research are: to propose a phylogenetic hypothesis for Mischonyx based on Total Evidence (TE); propose taxonomic changes based on the phylogeny; and analyze the phylogenetic hypothesis biogeographically. Using the exemplar approach to taxon selection, we studied 54 specimens, 15 outgroups and 39 ingroup taxa using seven molecular markers (28S, 12S and 16S ribosomal genes, citochrome oxidase subunit I gene, carbamoyl-phosphate synthetase gene, internal transcribed spacer subunit 2 and histone H3 gene), totaling 3,742 bp, and 128 morphological characters. We analyzed the dataset under three optimality criteria: Maximum likelihood (ML), Maximum parsimony (MP) and Bayesian. We discuss the transformation of character states throughout the phylogeny, the different phylogenetic hypotheses using different datasets and the congruence of evidence between the clades obtained by the phylogenetic analysis and the biogeographical hypothesis for the Atlantic Forest areas of endemism. We estimate that Mischonyx clade diverged 50.53 Mya, and inside the genus there are two major clades. One of them cointains species from Paraná, Santa Catarina, South of São Paulo and Serra do Mar Areas of Endemism and the other has species from Espinhaço, Bocaina, South coast of Rio de Janeiro and Serra dos Órgãos Areas of Endemism. The first split inside these two clades occurred at 48.94 and 44.80 Mya, respectively. We describe three new species from Brazil: Mischonyx minimus sp. nov. (type locality: Petrópolis, Rio de Janeiro), Mischonyx intervalensis sp. nov. (type locality: Ribeirão Grande, São Paulo) and Mischonyx tinguaensis sp. nov (type locality: Nova Iguaçu, Rio de Janeiro). The genus Urodiabunus Mello-Leitão, 1935 is considered a junior synonym of Mischonyx. Weyhia spinifrons Mello-Leitão, 1923; Weyhia clavifemur Mello-Leitão, 1927 and Geraeocormobius reitzi Vasconcelos, 2005 were transferred to Mischonyx. Mischonyx cuspidatus (Roewer, 1913) is a junior synonym of M. squalidus Bertkau, 1880. In the results of the phylogenetic analyses, Gonyleptes antiquus Mello-Leitão, 1934 (former Mischonyx antiquus) does not belong in Mischonyx and its original combination is re-established. As it is now defined, Mischonyx comprises 17 species, with seven new combinations.


Zootaxa ◽  
2021 ◽  
Vol 4915 (2) ◽  
pp. 201-236
Author(s):  
PRAKASH C. PATHANIA ◽  
CORNELIS GIELIS ◽  
APURVA DAS ◽  
KAILASH CHANDRA

A catalogue of the species of superfamily Pterophoroidea from India is presented. The documented fauna comprises 108 species belonging to two families, Macropiratidae (one species), and Pterophoridae (107 species in 38 genera). Four subfamilies of Pterophoridae are recognized: i) Agdistinae (one species), ii) Deuterocopinae (five species in one genus), iii) Ochyroticinae (three species in one genus), and iv) Pterophorinae (98 species in 35 genera). The present catalogue is based primarily on the literatures in which Indian pterophoroids have been mentioned or described. For each species, the type-locality, geographical distribution (within and outside of India), host plants, and synonyms are provided. Pterophorus karmawangdi Gielis & Wangdi, syn. n., is new subjective junior synonym of Pterophorus tinsuki Kovtunovich, 2003. 


Crustaceana ◽  
2019 ◽  
Vol 92 (5) ◽  
pp. 513-536
Author(s):  
Huiming Li ◽  
Shea K. P. Guinto ◽  
Rey D. S. Papa ◽  
Bo-Ping Han ◽  
Francis S. Magbanua ◽  
...  

Abstract The original description of Diaptomus vexillifer Brehm, 1933, endemic to Lake Danao (Leyte Island), was elementary and lacking taxonomically satisfactory characters. In this paper, we redescribe the Philippine-endemic genus Filipinodiaptomus Lai, Mamaril Sr. & Fernando, 1979 and the species D. vexillifer collected from its type locality, using light and scanning electron microscopy and an analysis of the mtCOI gene and the ITS of the nuclear 18S operon. We found that D. vexillifer is the second species under this endemic genus. A neotype and paraneotypes are hereby designated. Also a detailed morphological comparison is made between Filipinodiaptomus vexillifer (Brehm, 1933) comb. nov. and Filipinodiaptomus insulanus (Wright, 1928). Their taxonomic characters, interspecies relationship, and biogeography are likewise discussed.


Zootaxa ◽  
2015 ◽  
Vol 4058 (1) ◽  
pp. 145 ◽  
Author(s):  
JOSÉ A. LANGONE ◽  
ESTEBAN O. LAVILLA ◽  
RAFAEL O. DE SÁ ◽  
DARÍO CARDOZO

Zootaxa ◽  
2007 ◽  
Vol 1653 (1) ◽  
pp. 57-68 ◽  
Author(s):  
EIJIROH NISHI ◽  
KATSUHIKO TANAKA ◽  
YOSHIMI FUJIOKA ◽  
MASANORI SATO

Sigambra hanaokai (Kitamori 1960), originally described from Japan, was regarded as a junior synonym of S. tentaculata (Treadwell 1941), described from the Northwestern Atlantic Ocean. We studied Japanese materials and compared them with a recent redescription of S. tentaculata and with S. phuketensis Licher and Westheide, 1997, another similar species. The validity of S. hanaokai is confirmed. In order to avoid any further confusion, we redescribe the species based on topotype specimens collected in Hiroshima, Seto Inland Sea, Japan, the type locality of the species. Additionally, we emphasize the differences between S. hanaokai and S. phuketensis, particularly in regard to the relative length of the median antenna. Lastly, we summarize the recent systematic status of all species of the genus, and provide a table summarizing taxonomic characters.


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