A new replacement name for Bezverkhovia Gorochov, 2018 (Orthoptera: Gryllidae: Podoscirtinae)

2020 ◽  
Vol 29 (1) ◽  
pp. 58-59
Author(s):  
A.V. Gorochov ◽  
V.V. Izerskyy

The generic name Bezverkhovia Gorochov, 2018 assigned to the cricket genus from South America is a junior homonym of the generic name in Vietnamese Lepidoptera. The new replacement name Eubezverkhovia nom. nov. is proposed here instead of the aforementioned homonymic name. The following new combinations are also suggested: Eubezverkhovia lydia (Gorochov, 2018), comb. nov. and E.? huanchaca (Gorochov, 2017), comb. nov.

Phytotaxa ◽  
2013 ◽  
Vol 146 (1) ◽  
pp. 1 ◽  
Author(s):  
PETER B. HEENAN ◽  
ROB D. SMISSEN

The generic taxonomy of the Nothofagaceae is revised. We present a new phylogenetic analysis of morphological characters and map these characters onto a recently published phylogenetic tree obtained from DNA sequence data. Results of these and previous analyses strongly support the monophyly of four clades of Nothofagaceae that are currently treated as subgenera of Nothofagus. The four clades of Nothofagaceae are robust and well-supported, with deep stem divergences, have evolutionary equivalence with other genera of Fagales, and can be circumscribed with morphological characters. We argue that these morphological and molecular differences are sufficient for the four clades of Nothofagaceae to be recognised at the primary rank of genus, and that this classification will be more informative and efficient than the currently circumscribed Nothofagus with four subgenera.        Nothofagus is recircumscribed to include five species from southern South America, Lophozonia and Trisyngyne are reinstated, and the new genus Fuscospora is described. Fuscospora and Lophozonia, with six and seven species respectively, occur in New Zealand, southern South America and Australia. Trisyngyne comprises 25 species from New Caledonia, Papua New Guinea and Indonesia. New combinations are provided where necessary in each of these genera.


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. 


2020 ◽  
Vol 14 (2) ◽  
pp. 241-253
Author(s):  
David J. Mabberley

The vexing literary relationship between Kurt Sprengel and Friedrich Dietrich appears to have led to some of Dietrich’s work being willfully disregarded and subsequently forgotten/extinguished/suppressed. Examination of Dietrich’s oeuvre leads to the rehabilitation of fifteen of his new combinations, making securer by up to 175 years, some names in current use for largely New World plants. To take into account Dietrich’s work as a whole, four new combinations and three nomina nova are proposed with the help of authorities in the germane plant groups: Caamembeca andina (A.W. Benn.) J.F.B. Pastore & Mabb. (Bolivia), Callicarpa ekmanii I.E. Méndez & Mabb. (Cuba), Clematis wangiana Mabb., (Madagascar), Coleataenia pulchra (F. Dietr.) Mabb. & LeBlond (USA), Packera dubia (Spreng.) Trock & Mabb. (USA), Piper samainianum Mabb. (Peru), Rostellularia vahliana (Schult.) Mabb. (south Asia), for which a lectotype is designated, with other adjustments of names in Besleria (B. formosa now B. amabilis, tropical America), Oxalis (O. eckloniana now O. biloba, South Africa), Passiflora (P. arborea now P. magnoliifolia, Colombia), Ribes (R. ruizii now R. sylvestre, Chile), and possibly Tocoyena (South America), while further work on Lupinus is called for.


Zootaxa ◽  
2009 ◽  
Vol 2139 (1) ◽  
pp. 23-42
Author(s):  
PASCHOAL C. GROSSI ◽  
M. J. PAULSEN

The genus Sclerostomus Burmeister (Lucanidae: Lucaninae) of South America is redefined and restricted to species with a complex male genital capsule. Subgenera of Sclerostomus that lack this character are elevated to generic status, including Altitatiayus Weinreich with 5 species, Chileistomus Weinreich with 1 species, and Sclerostomulus Weinreich with 2 species. These genera are redescribed, and 2 new monotypic genera are created for species of Sclerostomus that cannot be accommodated into these existing genera. The subgenus Sclerostominus Weinreich is synonymized with Sclerostomus. Three species with simple male genitalic capsules are transferred to the genus Onorelucanus Bartolozzi & Bomans, resulting in the new combinations O. boileaui (Weinreich), O. marujae (Arnaud, Noguchi, & Bomans), and O. noguchii (Arnaud & Bomans). One species is transferred to Onorelucanus from the genus Scortizus Westwood, resulting in the combination O. pulverosus (Westwood). Scortizus ismaeli Fukinuki is placed in synonymy with O. pulverosus (Westwood).


Phytotaxa ◽  
2013 ◽  
Vol 96 (1) ◽  
pp. 63 ◽  
Author(s):  
S.K. SINGH

The subgenus Otigoniolejeunea Spruce (1884: 77) of Lejeunea Lib. (1820: 372) was initially described with five species, viz. L. acanthotis Spruce (1884: 227), L. cyrtotis Spruce (1884: 227), L. quinqueumbonata Spruce (1884: 227), L. schizotis Spruce (1884: 227) and L. xiphotis Spruce (1884: 227), all from South America. A few years later, the subgenus was upgraded to genus level by Schiffner (1895) who made the combinations Otigoniolejeunea xiphotis (Spruce) Schiffn. (1895: 125) and O. schizotis (Spruce) Schiffn. (1895: 125). The former species was designated as the lectotype of Otigoniolejeunea by Vanden Berghen (1948).


Phytotaxa ◽  
2020 ◽  
Vol 477 (2) ◽  
pp. 102-150
Author(s):  
ANA MARIA GIULIETTI

Previous morphological and molecular studies indicate that the genus Leiothrix is a monophyletic and well supported clade in Eriocaulaceae. A taxonomic revision of the genus for the Flora Neotropica is in progress, but with the Flora do Brasil 2020 project now in its final stages, this synopsis became necessary to present an updated list of accepted species, their synonyms and typifications. Protologues and types of 122 previously published names have been reviewed. The genus now includes 39 species and six varieties, adding up to 42 taxa endemic to Brazil, occurring especially in the Espinhaço Range in Minas Gerais and Bahia States. One species extends from Brazil to other countries of northern South America and one species and one variety are found only in Venezuela. In this paper I propose 34 new synonyms, five new combinations, three changes of status, one neotype and 49 lectotypes.


Zootaxa ◽  
2007 ◽  
Vol 1458 (1) ◽  
pp. 1-80 ◽  
Author(s):  
ANDREW B.T. SMITH ◽  
PAUL E. SKELLEY

The 27 Aphodiinae (Coleoptera: Scarabaeidae) species that occur in southern South America are reviewed. This study region consists of the southern parts of Argentina and Chile including the Central Chilean, Patagonian, and Subantarctic biogeographical provinces. Keys, illustrations, and distributional records with maps for all species are presented. Seventeen species are native to southern South America, nine species are introduced, and the status of one species could not be determined due to a lack of study material. Nine of the 17 native species are endemic to southern South America, and the relationship between these endemic species and similar Australian groups is discussed. A number of classification and nomenclatural changes are made. Paranimbus Schmidt and Pseudopodotenus Dellacasa are considered to subgenera of Podotenus Schmidt. As a result, the following new combinations are created: Podotenus (Paranimbus) longitarsis (Harold), Podotenus (Paranimbus) penai (Petrovitz), Podotenus (Paranimbus) peruanus (Erichson), Podotenus (Paran- imbus) zoiai (Dellacasa), and Podotenus (Pseudopodotenus) fulviventris (Fairmaire and Germain). Ataenius chilensis (Solier) is removed from synonymy with Ataenius gracilis (Melsheimer) and is considered a valid species. Ataenius modestus Schmidt is synonymized under Ataenius chilensis (Solier). Psammobius indefensus Schmidt is transferred to the genus Leiopsammodius and Leiopsammodius chilensis Rakovic is placed in synonymy with this name. Lectotypes are designated for the following names: Aphodius chilensis Solier (now Ataenius chilensis), Aphodius reflexus Schmidt (now Orodaliscoides reflexus), Ataenius modestus (now a synonym of Ataenius chilensis), and Psammobius indefensus Schmidt (now Leiopsammodius indefensus). A neotype is designated for Aphodius angustus Philippi and Philippi, a synonym of Pleurophorus caesus (Panzer). Records considered to be erroneous for several Aphodiinae species in southern South America are also discussed.


Zootaxa ◽  
2010 ◽  
Vol 2607 (1) ◽  
pp. 1
Author(s):  
KEVIN M. PITZ

Herein I describe 16 new species of Capitonius and formally transfer and redescribe the species Foenomorpha bicolor Szépligeti, F. senlura Braet and Achterberg, and F. rufa Braet and Achterberg to Capitonius as Capitonius bicolor, C. senlura, and C. rufa, new combinations. The following new species are described: Capitonius bellaptera Pitz n. sp. from Brazil, C. boringi Pitz n. sp. from South America, C. catemacoensis Pitz n. sp. from Mexico, C. flavusassumentum Pitz n. sp. from Argentina, C. lateventris Pitz n. sp. from Brazil, C. negrolabiatus Pitz n. sp. from Central and South America, C. nigrum Pitz n. sp. from South America, C. robertsonae Pitz n. sp. from Brazil, C. rondoniaensis Pitz n. sp. from Brazil, C. sarmientoi Pitz n. sp. from Colombia, C. seltmannae Pitz n. sp. from Colombia, C. sharkeyi Pitz n. sp. from Colombia, C. stramentopetiolus Pitz n. sp. from French Guyana, C. stramentosura Pitz n. sp. from Central and South America, C. venezuelaensis Pitz n. sp. from Venezuela, and C. venustus Pitz n. sp. from South America. A key to species of subgenus Foenomorpha is provided.


2020 ◽  
Vol 62 (3-4) ◽  
pp. 293-307
Author(s):  
S. Y. Kondratyuk ◽  
L. Lőkös ◽  
M.-H. Jeong ◽  
S.-O. Oh ◽  
A. S. Kondratiuk ◽  
...  

Three genera new for science, i.e. Candelinella S. Y. Kondr. for the Candelariella makarevichiae group, Opeltiella S. Y. Kondr. for the Candelaria fraudans group, as well as Protocandelariella Poelt, D. Liu, J.-S. Hur et S. Y. Kondr. for the Candelariella subdeflexa group are proposed for robust monophyletic branches of the Candelariaceae on the basis of three-gene phylo- geny (i.e. concatenated nrITS, 12S mtSSU and 28S nrLSU sequences). Eight new combinations, i.e. Candelinella makarevichiae (for Candelariella makarevichiae S. Y. Kondr., L. Lokos et J.-S. Hur), Candelinella deppeanae (for Candelariella deppeanae M. Westb.), Opeltiella fraudans (for Candelaria fraudans Poelt et Oberw.), Opeltiella fibrosoides (for Candelaria fibrosoides M. Westb. et Froden), Opeltiella rubrisoli (for Candelariella rubrisoli D. Liu et J.-S. Hur), Opeltiella canadensis (for Candelariella canadensis H. Magn.), Protocandelariella subdeflexa (for Lecanora subdeflexa Nyl.), Protocandelariella blastidiata (for Candelariella blastidiata L. Yakovchenko) are provided.Molecular data provided for Candelinella makarevichiae (including holotype and iso- type), as well as additional specimens of Candelaria asiatica from South Korea for the first time. The latter species (Candelaria asiatica) from China, as well as’Candelaria’ murrayi from Argentina, South America are recorded for the first time. Voucher of Candelariella vitellina from Antarctica is also identified based on molecular phylogeny. It is for the first time shown that ’Candelaria’murrayi is positioned in the outermost position to Candelaria s. str. branch of the phylogenetic tree of the Candelariaceae, and may belong to another genus. Status of the ’Candelariella’medians group, the’Candelariella’ placodizans group, as well as single species ’Candelariella’reflexa and’Candelaria’ pacifica, forming separate branches outside the Candelariella s. str. and Candelaria s. str. clades, will be clarified when additional molecular data will be accumulated. Candelariella subsquamulosa D. Liu et Hur, recently described from South Korea (Liu et al. 2019), proved to be a new synonym of Candelinella makarevichiae.


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