Reinstatement of Sigambra hanaokai (Kitamori, 1960) (Polychaeta, Pilargidae), with an overview of the literature on the genus

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.

Zootaxa ◽  
2019 ◽  
Vol 4608 (1) ◽  
pp. 90
Author(s):  
JOANA SANDES ◽  
RADHARANNE RECINOS ◽  
ULISSES PINHEIRO ◽  
GUILHERME MURICY

The demosponge genus Endectyon is characterized by the presence of acanthostyles with recurved or clavulate spines. Two subgenera are recognized, Endectyon and Hemectyon, distinguished mainly by the acanthostyles being located only in the periphery of the axial skeleton in Endectyon, or forming the ectosomal brushes in Hemectyon. Sixteen species are known worldwide, of which only two were reported from the Western Atlantic Ocean. However, the type locality of Endectyon xerampelina is uncertain, and it could be located either in the Western Atlantic or in Australia. In the present study, we describe new records of E. xerampelina from the Brazilian coast and propose that Raspailia (R.) johnhooperi from the Guyana shelf is a junior synonym of E. xerampelina. Our results support the hypothesis that the type locality of E. xerampelina is located somewhere in the Tropical Western Atlantic Ocean and also that the species belongs to the subgenus Endectyon (Endectyon). We amended the diagnosis of the subgenus Endectyon (Endectyon) to account for the variability of acanthostyle shape in E. (E.) xerampelina, assigning greater taxonomic value to the position of the echinating megascleres than to their shape and pattern of spination. 


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 ◽  
2017 ◽  
Vol 4254 (3) ◽  
pp. 357 ◽  
Author(s):  
DANIEL CHIRIVI JOYA

We present the description of Phrynus calypso sp. nov. from Trinidad and Tobago, and Venezuela This species is very similar to Phrynus pulchripes (Pocock), however after examining Colombian specimens of P. pulchripes (ca. type locality), many differences were found. Characters commonly used in diagnosis of Phrynus species are variable and make identification difficult. Differences in a few structures, like pedipalpal spines, could not be enough to provide a useful diagnosis.  It is necessary to account for variation of similar species in conjunction, and select non overlapping groups of characters. Observations in the variation in both species are presented, pointing out sources of confusion, and suggesting alternative characters to support diagnoses. At the moment, details about variation in many species in Phrynus, like that of P. pulchripes, are poorly known, and for this reason a redescription is provided. 


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. 


Zootaxa ◽  
2005 ◽  
Vol 916 (1) ◽  
pp. 1 ◽  
Author(s):  
LUIS E. ACOSTA

The long neglected scorpion species Orobothriurus bivittatus (Thorell) stat. n., comb. n. (Bothriuridae), formerly considered a subspecies of Urophonius brachycentrus (Thorell) and more recently placed under synonymy of the type species of Orobothriurus Maury, O. alticola (Pocock), is revalidated and redescribed on a male captured in the Sierra del Tontal, west Argentina. It proved to be a close relative of O. alticola, from which it can be separated by some details of the hemispermatophore morphology (e.g. relative length of the lamina apex, lobular expansions at the inflexion point of the front crest). This species is probably a high altitude endemic to the Precordillera, a range separated from the Andes (where O. alticola was collected) by a narrow valley. The type locality for O. bivittatus stat. n., comb. n. (and also for Telegonus weijenberghi Thorell) is restricted to the upper belts of the mentioned range, as thoroughly discussed. To ensure nomenclatural stability, it is proposed to set aside the existing holotype and to designate the studied male as neotype.


Zootaxa ◽  
2020 ◽  
Vol 4742 (3) ◽  
pp. 401-441
Author(s):  
BENEDITO MENDES NUNES ◽  
LOURIVAL DIAS CAMPOS ◽  
MARIA THAYANE DA SILVA MENDONCA ◽  
EDUARDO VICTOR DE PAIVA CUNHA ◽  
JOSE ANTONIO MARIN FERNANDES

Hypoxys is one of four subgenera of Edessa (Fabricius, 1787) together with Aceratodes (De Geer, 1773), Dorypleura (Lepeletier & Serville, 1825) and Edessa (Fabricius, 1787). This taxon has a very confusing taxonomy due to incorrect use of the names available, imprecise descriptions, and large number of very similar species. To illustrate the confusion, Hypoxys potentially includes a large number of species of Edessa, but actually contains only the type species, according to the most recent catalogue. The name E. quadridens Fabricius, 1803, type species of Hypoxys, was used for more than a century as a label to identify a large group of similar species. In this work we continue revising Edessa elevating Hypoxys to genus based on the following morphological characters: proximal part of costal margin black; evaporatorium with a deep notch on lateral margin; anterior arms of metasternal process acuminate; pygophore longer than wide and subrectangular or barrel-shaped in dorsal view; dorsal rim of pygophore well-projected, almost reaching posterolateral angles and finishing in a small lobe; and posterolateral angles of pygophore not developed. Hypoxys is being divided in four species groups to include 17 species transferred from Edessa. H. quadridens group comprises: Hypoxys quadridens (Fabricius, 1803) (type species), H. boerneri (Breddin, 1904) comb. nov., H. claricolor (Breddin, 1907) comb. nov., H. dolosus (Breddin, 1907) comb. nov., H. eburatulus (Breddin, 1907) comb. nov., H. necopinatus (Breddin, 1907) comb. nov., H. offuscatus (Breddin, 1907) comb. nov. and H. trabeculus (Breddin, 1907) comb. nov. H. triangularis group comprises: H. triangularis (Dallas, 1851) comb. nov. (type species), H. capito (Breddin, 1904) comb. nov. and H. subrastratus (Bergroth, 1891) comb. nov. H. oxyacanthus group comprises: H. oxyacanthus (Breddin, 1904) comb. nov. (type species), H. brachyacanthus (Breddin, 1904) comb. nov., H. infulatus (Breddin, 1904) comb. nov., H. leptacanthus (Breddin, 1904) comb. nov. and H. tragelaphus (Breddin, 1903) comb. nov. H. balteatus group comprises only H. balteatus (Walker, 1868) comb. nov. These groups of species will be useful to organize the new species of Hypoxys that will be described in upcoming papers. Descriptions, measurements, photos of genitalia of both sexes; photos in dorsal and ventral views of the species; and distribution maps are provided. Males of H. capito, H. claricolor, H. eburatulus, H. infulatus, and H. subrastratus are described for the first time. Female of H. necopinatus is described for the first time. Edessa jugalis is considered a junior synonym of H. quadridens; E. rimata a junior synonym of H. offuscatus; E. scabriventris and E. leprosula junior synonyms of H. triangularis; E. pachyacantha a junior synonym of H. tragelaphus; E. orba a junior synonym of E. oxyacanthus. A key to the species of Hypoxys is also provided. 


2011 ◽  
Vol 102 (1) ◽  
pp. 43-50 ◽  
Author(s):  
M. Gebiola ◽  
M. Giorgini ◽  
P. Navone ◽  
U. Bernardo

AbstractWe provide a karyological study of 12 species of the genus Pnigalio in an attempt to evaluate the taxonomic utility of karyotypes at the species level. For all species of Pnigalio examined the number of chromosome was 2n=12. Karyotype formulae presented mainly metacentric and submetacentric chromosomes, although a pair of acrocentrics or subtelocentrics, shorter than biarmed chromosomes, was present in some species. The analysis of karyotypes of Pnigalio showed frequent but not general interspecific variability of the chromosome traits. Although most of the studied species revealed concordance between morphological and karyological characters (centromeric index and relative length), two other categories have been identified: morphologically distinct species without reciprocal differences in karyotype structure, and morphologically similar species that strongly differ in chromosomal characters.


Zootaxa ◽  
2018 ◽  
Vol 4471 (2) ◽  
pp. 245 ◽  
Author(s):  
VÍCTOR M. CONDE-VELA

Pseudonereis gallapagensis Kinberg, 1865 and P. variegata (Grube & Kröyer in Grube, 1858) are the only two species of this genus commonly recorded along Atlantic American coasts, but their type localities are in the Eastern Pacific, and their morphology differs. Two new Pseudonereis species are described from Eastern Mexico: P. brunnea sp. n. from the Gulf of Mexico, and P. citrina sp. n. from the Caribbean Sea, previously confused with P. gallapagensis. In order to facilitate comparisons, descriptions based on specimens from near the type locality for P. gallapagensis (Peru and Ecuador), and topotypes for P. variegata (Valparaiso, Chile), are included. Based on these comparisons and current descriptions, the synonymies of Nereis ferox Hansen, 1882 described from Brazil with P. variegata, and of Pseudonereis formosa Kinberg, 1865 described from Hawaii with P. gallapagensis, are rejected. Consequently, both are regarded as distinct species and revised diagnoses are provided for them. The record of P. ferox from the Gulf of Guinea proved to be an undescribed species, and is herein described as P. fauveli sp. n. The number of paragnath rows in nereidid pharynx areas VII–VIII has been interpreted in several ways, leading to confusion; an alternative method to determine the number of bands and rows is proposed. The midventral region, the division of areas VII–VIII in furrow and ridge regions, and the description of the arrangement based on the pattern of paragnaths in such regions, are proposed. Further, the terms shield-shaped and pointed (P-bars) bars are redefined, and a new term, crescent-shaped bars, is proposed for paragnaths in the areas VI in some Pseudonereis and Perinereis species. A key for all Pseudonereis species is also included. 


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