Vanapina lineata de Vis 1905 Is a Junior Synonym of the New Guinean Snake Toxicocalamus longissimus Boulenger, 1896

Copeia ◽  
1989 ◽  
Vol 1989 (3) ◽  
pp. 753 ◽  
Author(s):  
Glen J. Ingram
Keyword(s):  
1991 ◽  
Vol 2 (2) ◽  
pp. 52
Author(s):  
Olof Biström ◽  
Mario Franciscolo ◽  
Nino Sanfilippo
Keyword(s):  

Entomologica Fennica. Vol. 2:52. 27.VIII.1991


2020 ◽  
Vol 71 (2) ◽  
pp. 149-150
Author(s):  
David Agassiz

The case for retaining Paraswammerdamia ruthiella Steuer, 1993 as a good species is reviewed. It should be regarded as a junior synonym of P. albicapitella (Scharfenberg, 1805), since there is no further evidence that it is a distinct species.


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 ◽  
2012 ◽  
Vol 3280 (1) ◽  
pp. 1 ◽  
Author(s):  
AMAZONAS CHAGAS-JÚNIOR

Three new species of Otostigmus Porat, 1876 from Brazilian Atlantic Forest are described. Otostigmus beckeri sp. n. andO. lanceolatus sp. n. are described from the state of Bahia and O. giupponii sp. n. from the state of Espírito Santo. InBrazil, the otostigmine scolopendrid genus Otostigmus comprises 22 species. A summary of Brazilian Otostigmus speciesis presented with new distribution records, taxonomic remarks when appropriate and an identification key. Otostigmus sul-catus Meinert, 1886 is recorded for the first time from Brazil; the Andean Otostigmus silvestrii Kraepelin 1903, previouslyrecorded from Brazil, is here considered not to be present in this country. Eight nominal species are regarded here as newsynonyms. Five of them—Otostigmus pradoi Bücherl, 1939, O. longistigma Bücherl, 1939, O. longipes Bücherl, 1939,O. langei Bücherl, 1946 and O. dentifusus Bücherl, 1946—are based on females of O. tibialis Brölemann, 1902. O. latipesBücherl, 1954 is conspecific with and is considered a junior synonym of O. sulcatus Meinert, 1886; O. limbatus diminutusBücherl, 1946 is a junior synonym of O. limbatus Meinert, 1886 and O. fossulatus Attems, 1928 is a junior synonym of O. goeldii Brölemann, 1898. A lectotype is designated for O. goeldii.


Zootaxa ◽  
2019 ◽  
Vol 4646 (1) ◽  
pp. 124-144
Author(s):  
FERNANDO MASSAYUKI ASSEGA ◽  
JOSÉ LUÍS OLIVAN BIRINDELLI

A taxonomic revision of Anostomoides is herein presented based on a comprehensive revision of specimens deposited in fish collections and the literature. The present revision proposes that A. laticeps is a junior synonym of A. atrianalis, while A. passionis is a junior synonym of Leporinus nattereri, and the latter is thus transferred to Anostomoides, forming the new combination Anostomoides nattereri. Principal Components Analysis (PCA) showed that examined specimens form two distinct morphotypes, corroborating the validity of both A. atrianalis and A. nattereri. Anostomoides nattereri is distinguished from A. atrianalis by having four branchiostegal rays (vs. three), three pores in infraorbital one (vs. four), 37–39 pored lateral-line scales (vs. 41–44), lower lip with rounded dermal papillae (vs. forming ridges), three dark  rounded midlateral blotches (vs. three or four vertically elongated blotches and/or a faded dark longitudinal stripe), dark lines between scale series on posterior half of body on specimens smaller than 150 mm SL (vs. dark lines absent), a greater body depth (27.6–36.2 % vs. 24.5–38.7% of SL) and smaller interorbital distance (34.4–53.8 % vs. 42.6–67.3 % of HL). Anostomoides nattereri is distributed across several tributaries of the Amazon and Orinoco rivers, whereas A. atrianalis is widespread throughout the Amazon, Orinoco, and Essequibo basins. The genus Anostomoides is currently diagnosed based on a combination of non-exclusive characters: upturned or slightly upturned mouth with four premaxillary teeth including symphyseal tooth bicuspid or with blunt cutting edge, remaining teeth slightly tricuspid (with medial cuspid distinctly larger); four dentary teeth, symphyseal tooth with truncate cutting edge (without cusps); second tooth with a single large cusp, and two lateral teeth with three or slightly more small cusps. 


2021 ◽  
pp. 1-2
Author(s):  
Philip M. Novack-Gottshall ◽  
Roy E. Plotnick

The horseshoe crab Limulus polyphemus (Linnaeus, 1758) is a famous species, renowned as a ‘living fossil’ (Owen, 1873; Barthel, 1974; Kin and Błażejowski, 2014) for its apparently little-changed morphology for many millions of years. The genus Limulus Müller, 1785 was used by Leach (1819, p. 536) as the basis of a new family Limulidae and synonymized it with Polyphemus Lamarck, 1801 (Lamarck's proposed but later unaccepted replacement for Limulus, as discussed by Van der Hoeven, 1838, p. 8) and Xyphotheca Gronovius, 1764 (later changed to Xiphosura Gronovius, 1764, another junior synonym of Limulus). He also included the valid modern genus Tachypleus Leach, 1819 in the family. The primary authority of Leach (1819) is widely recognized in the neontological literature (e.g., Dunlop et al., 2012; Smith et al., 2017). It is also the authority recognized in the World Register of Marine Species (WoRMS Editorial Board, 2021).


Zootaxa ◽  
2009 ◽  
Vol 2318 (1) ◽  
pp. 566-588 ◽  
Author(s):  
DANIEL WHITMORE

An account is given of the species of Sarcophaga Meigen, 1826 subgenus Heteronychia Brauer & Bergenstamm, 1889 known from the island of Sardinia (Italy). Most of the nearly 1,400 specimens examined were collected in the SW part of the island during 2003–2006 as part of a project investigating the arthropod diversity of the Monti Marganai and Montimannu areas (respectively Carbonia-Iglesias and Medio Campidano provinces). The study resulted in the finding of eight species of Heteronychia, six of which are recorded from Sardinia for the first time. Sarcophaga (Heteronychia) penicillata Villeneuve, 1907, previously mentioned in the literature, is excluded from the fauna of the island. Sarcophaga (Heteronychia) thirionae (Lehrer, 1976) is recorded for the first time from Europe and North Africa (Algeria). One species, Sarcophaga (Heteronychia) gabrielei sp. nov., from various sites in the limestone massif of Marganai, is described as new. Previously unpublished records from other Italian regions and from other countries (Algeria, Canary Islands, Greece) are also given for several species. Sarcophaga (Heteronychia) schnabli Villeneuve, 1911 is recognized as a junior synonym of S. (H.) consanguinea Rondani, 1860 syn. nov. The possible synanthropy of Sarcophaga (Heteronychia) pandellei (Rohdendorf, 1937) is briefly discussed. A key to males and females of all known Sardinian and Corsican species of Sarcophaga (Heteronychia) is provided.


Zootaxa ◽  
2011 ◽  
Vol 2983 (1) ◽  
pp. 39 ◽  
Author(s):  
IVAN L. F. MAGALHÃES ◽  
ADALBERTO J. SANTOS

In this paper, M. yanomami n. sp., from Brazilian Amazonia, Chaetacis bandeirante n. sp., from Central Brazil, and the males of M. gaujoni Simon, 1897 and M. ruschii (Mello-Leitão, 1945) n. comb. , respectively from Ecuador and Brazil, are described and illustrated for the first time. An ontogenetic series of the last development stages of both sexes of Micrathena excavata (C. L. Koch, 1836) is illustrated and briefly described. Adult females are larger and have longer legs and larger abdomens than adult males. Probably females undergo at least one additional moult before adulthood, compared to males. Micrathena ornata Mello-Leitão, 1932 is considered a junior synonym of M. plana (C. L. Koch, 1836), and M. mastonota Mello-Leitão 1940 is synonymized with M. horrida (Taczanowski, 1873). Acrosoma ruschii Mello-Leitão, 1945 is revalidated, transferred to Micrathena and considered a senior synonym of M. cicuta Gonzaga & Santos, 2004. Chaetacis necopinata (Chickering, 1960) is recorded for Brazil for the first time. Chaetacis incisa (Walckenaer, 1841) is considered a nomen dubium.


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