Rediscovery and redescription of the Andean earth-snake Atractus wagleri (Reptilia: Serpentes: Colubridae)

Zootaxa ◽  
2009 ◽  
Vol 1969 (1) ◽  
pp. 59-68 ◽  
Author(s):  
PAULO PASSOS ◽  
JUAN C. ARREDONDO

Atractus wagleri was described based on a single specimen from Humbo, Department of Boyacá on the western Cordillera Oriental of Colombia, and since its original description there is no further record for the species. In the course of examination of Colombian collections the holotype of the Atractus wagleri could not be found and it is probable that it was lost, but we found three additional specimens of this poorly known snake from localities relatively close to the type locality. In this paper, we describe these specimens, and report data on meristics, morphometrics, and hemipenial variation for the species.

Check List ◽  
2013 ◽  
Vol 9 (4) ◽  
pp. 820
Author(s):  
Adriana Almirón ◽  
Jorge Casciotta ◽  
María Cecilia Bruno ◽  
Lubomír Piálek ◽  
Klára Doubnerová ◽  
...  

Leporinus amae is known from the Rio Apuaê (type locality), Rio Canoas and Rio Caveiras tributaries of the Uruguay River basin, in Brazil. The original description of this species was mainly based on a single specimen lacking intraspecific variation in meristic and morphometric of most characters. We expand the range of distribution and report the first occurrence of Leporinus amae in Misiones Province, Argentina. Additionally, we provide a supplementary description of the species.


Zootaxa ◽  
2019 ◽  
Vol 4543 (2) ◽  
pp. 295
Author(s):  
PETER GEISSLER ◽  
ALEXANDER KUPFER

The species Lygosoma (Keneuxia) dubium was described by Franz Werner (1909) based on a single specimen from the Royal Natural History Cabinet (Königliches Naturalienkabinett) in Stuttgart, collection number 3651. According to the original description the specimen was collected by “Direktor Mayer” in Yokohama, Japan in 1897. Much later Nakamura & Ueno (1963) transferred the species to the Genus Dasia Gray, 1839, without further comments. Recently Uetz et al. (2018) questioned the type locality given by Werner (1909) and suggested that the name Lygosoma dubium is likely to be a synonym of Dasia grisea (Gray, 1845) referring to a personal comment of T. Hikida in 2014. However the actual taxonomic status of the species still remains unresolved. 


ENTOMON ◽  
2019 ◽  
Vol 44 (1) ◽  
pp. 23-32 ◽  
Author(s):  
P. C. Sujitha ◽  
G. Prasad ◽  
R. Nitin ◽  
Dipendra Nath Basu ◽  
Krushnamegh Kunte ◽  
...  

Eurema nilgiriensis Yata, 1990, the Nilgiri grass yellow, was described from Nilgiris in southern India. There are not many published records of this species since its original description, and it was presumed to be a high-elevation endemic species restricted to its type locality. Based on the external morphology (wing patterns) as well as the male genitalia, the first confirmed records of the species from Agasthyamalais and Kodagu in the southern Western Ghats, is provided here. This report is a significant range extension for the species outside the Nilgiris, its type locality. Ecological data pertaining to this species as well as the field identification key to all known Eurema of Western Ghats are also presented.


2015 ◽  
Vol 42 (2) ◽  
pp. 226-235 ◽  
Author(s):  
G. N. H. Waller

Eight species of mesoplodont whales (genus Mesoplodon Gervais, 1850) named during the nineteenth century are based on valid descriptions. A checklist with the original description and type material for each of these species is provided. Additional data given may include type locality and illustrative sources, type material holding institution and type registration number(s). The only type specimen for which a record of external morphology was published relates to the 1803 stranding of Sowerby's beaked whale (Mesoplodon bidens).


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. 


2018 ◽  
Vol 26 ◽  
pp. 55-66
Author(s):  
Boyan Vagalinski ◽  
Kaibaryer Meng ◽  
Darina Bachvarova ◽  
Pavel Stoev

We redescribe the poorly known Chinese millipede Skleroprotopusmembranipedalis Zhang, 1985 recorded from Shi-Hua (Stone Flower) Cave, Fangshan County, Beijing. The species’ original description is in Chinese in an obscure outlet which significantly hampers its recognition from its congeners. Here, based on newly collected material, we provide the first scanning electron micrographs of important taxonomic traits. In addition to its type locality, we report the species also from Yun-Shui (Cloud Water) Cave, situated in the same county, some 18 km away. We propose the genus Senbutudoiulus Miyosi, 1957 to be a junior subjective synonym of Skleroprotopus Attems, 1901, syn. n., and introduce the following new combination: Skleroprotopusplatypodus (Miyosi, 1957), comb. n. (former Senbutudoiulus).


Crustaceana ◽  
2018 ◽  
Vol 91 (6) ◽  
pp. 677-731
Author(s):  
Yenumula Ranga Reddy

Abstract Only eight groundwater crustacean species were known in India till the end of 20th century. Analysis of about 4000 samples collected during 2000-2016 from diverse groundwater habitats, especially in certain pockets of the deltaic belt of the Rivers Krishna and Godavari in the southeastern peninsular India, has so far yielded about 90 new crustacean taxa. Of these, 67 new species have been described formally, which include, respectively, 34, 27, 3, 2 and 1 species each of Copepoda, Bathynellacea, Amphipoda, Isopoda and Ostracoda. The updated checklist presented herein includes a total of 87 species in 45 genera, 22 families and 8 orders. For each species, the reference to its original description, type locality, distribution, and ecological notes, co-occurring fauna, if any, and sampling method(s) are given. Besides map-pointing the type localities of the species, brief notes are given on the biogeography and conservation.


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 ◽  
2012 ◽  
Vol 3475 (1) ◽  
pp. 86 ◽  
Author(s):  
ALBERTINA P. LIMA ◽  
LUCIANA K. ERDTMANN ◽  
ADOLFO AMÉZQUITA

Allobates crombiei was described by Morales, “2000” [2002] based on specimens collected by Ronald I. Crombie from Cachoeira do Espelho, on the right bank of the Xingu River, Pará State, Brazil. The original description was short and did not include the call or colour in life. Rodrigues & Caramaschi (2004) suggested that the taxonomic status of this species need be clarified. We are confident that the species collected and recorded by us is Allobates crombiei (Morales) “2000” [2002] because this is the only species of Allobates found calling in forest near Cachoeira do Espelho, and the character diagnosis in preserved specimens is similar, except that, based on preserved specimens, Morales (2002) considered the ventrolateral and the oblique lateral stripes to be absent. This may be because they are imperceptible in preserved specimens. However, unlike recent authors, Morales (2002) also considered the oblique lateral stripe to be absent in Allobates brunneus, Allobates gasconi and Allobates ornatus, in which he illustrated diffuse spots.


Zootaxa ◽  
2019 ◽  
Vol 4623 (3) ◽  
pp. 595-600 ◽  
Author(s):  
JHONATTAN VANEGAS-GUERRERO ◽  
ANGELE MARTINS ◽  
ESTEBAN QUIÑONES-BETANCURT ◽  
JOHN D. LYNCH

The fossorial snake genus Anomalepis Jan 1860 currently comprises four species with distribution restricted to the Neotropics, occurring from Nicaragua to trans-Andean Peru. Species of Anomalepis occur on the mainland from sea level to about 2,700 m elevation in habitats that range from xerophyte vegetation to tropical wet forests (Kofron 1988; McDiarmid et al. 1999; Uetz et al. 2019; Wallach et al. 2014). Kofron (1988) performed a taxonomic review of the genus Anomalepis, recognizing two phenotypic clusters of species: the A. mexicanus Jan 1860 composed exclusively by its nominal form, and the A. aspinosus Taylor 1939 group consisting of the former species, A. colombia Marx 1953 (Fig. 1) and A. flavapices Peters 1957. While Anomalepis aspinosus occurs in xerophytic formation from 500–2700 above sea level (asl hereafter) along the Peruvian Andes (Kofron 1988; McDiarmid et al. 1999; Wallach et al. 2014), and Anomalepis flavapices is found in the coastal rainforest plains of northwestern Ecuador (Kofron 1988; Wallach et al. 2014), Anomalepis mexicanus presents the most widespread distribution amongst its congeners, occurring in northeastern Honduras, Nicaragua, Costa Rica and Panama from sea level to 725 m altitude. Even though this species has previously been recorded for Peru (Kofron, 1988), it seems unlikely that this specimen belongs to A. mexicanus due to its distinct meristic features (see Kofron 1988) and its outlandish record (see Fig. 2). Marx (1953) described Anomalepis colombia based on a single specimen collected in 1946 by Kjell von Sneidern at La Selva (05º25’23N, 74º57’44W; 1700 m asl), municipality of Pueblo Rico, department of Caldas, Colombia. As far as we know, since its original description, no additional specimen of A. colombia has been reported in literature (cf. Kofron 1988; McDiarmid et al. 1999; Wallach et al. 2014). 


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