A revised and geo-referenced list of type localities for termites in South America

Zootaxa ◽  
2019 ◽  
Vol 4638 (3) ◽  
pp. 389-409
Author(s):  
REGINALDO CONSTANTINO

A revised, geo-referenced, and cross-referenced list of 270 termite type localities in South America is presented. A total of 543 nominal species-group extant taxa are listed, 442 of them valid and 97 synonyms. The type-locality comprising the greatest number of nominal taxa in South America is Kartabo, Guyana (A.E. Emerson study site), with 59 taxa, followed by Cuiabá, Brazil (F. Sivestri), with 34, and Ribeirão Cascalheira, Brazil (Xavantina-Cachimbo Expedition, A.G.A. Mathews) with 26. 

Acarologia ◽  
2021 ◽  
Vol 61 (4) ◽  
pp. 1023-1035
Author(s):  
Henri M. André

An online database on the taxonomy of Tydeoidea is described and is available on the Wikispecies platform at https://species.wikimedia.org/wiki/Tydeoidea. It counts 1 324 records or pages, 724 records for the Tydeidae, 334 for the Ereynetidae, 203 for the Iolinidae and 63 for the Triophtydeidae. For each taxon are detailed the parent taxa as well as the child taxa which are listed. A nec subsection lists names of child taxa that are not recommended. Subjective and objective synonymies as well as homonymies are given for each taxon. Notes provide historical aspects of past studies. The type locality and habitat of the name-bearing type and its repository are added for the nominal species-group taxa. Fossil species, species inquirendae and nomina nuda are also reported. References and external links end up a record. Tetranychus viburni Koch is resurrected from synonymy with Tetranychus urticae Koch and placed in Tydeidae; it might be a senior synonym of Tydeus goetzi Schruft. Replacement names are provided for Aureliana and Tydides (homonymy) and for Paratydaeolus clavatus (synonymy).


Zootaxa ◽  
2019 ◽  
Vol 4576 (3) ◽  
pp. 439 ◽  
Author(s):  
ANTOINE FOUQUET ◽  
JEAN-PIERRE VACHER ◽  
ELODIE A. COURTOIS ◽  
CHLOÉ DESCHAMPS ◽  
PAUL OUBOTER ◽  
...  

Anomaloglossus is a species-rich genus of frogs endemic to the Guiana Shield that still harbors several unnamed species. Within the A. stepheni species group (which includes four valid nominal species), A. baeobatrachus has an uncertain taxonomic status, notably because the holotype was an unvouchered specimen depicted in a popular journal. Another member of this group, A. leopardus, was only superficially described, lacking information on the sex of specimens in the type series and on advertisement call. Therefore, these two taxa need clarifications in order to allow the description of the extant undescribed species. In this paper, we redescribe A. baeobatrachus based on newly collected material from the species type locality and provide information about its reproductive ecology. We also provide an amended definition of A. leopardus using newly collected material from its type locality. These two species form a clade along with a third species from the Eastern Guiana Shield, which is also described herein. The reproductive biology of A. baeobatrachus and A. stepheni is very similar. Both species have endotrophic and nidicolous tadpoles, despite being distantly related, suggesting independent evolution of this breeding mode. The new species and A. leopardus, on the other hand, have exotrophic tadpoles. 


2006 ◽  
Vol 35 ◽  
Author(s):  
Keti M.R. Zanol

In the General Catalogue of the Homoptera (METCALF, 1967)contains 36 genera and 215 Neotropical species, including north ofMexico distributed within 10 tribes (two genera and six species inEuscelini, one genera and one species in Colladonini, one genusand one species in Goniagnathini, four genera and 52 species inAcinopterini, one genus and one species in Cicadulini, four generaand 80 species in Scaphytopiini, five genera and 32 species inBalcluthini, one genus and one species in Macrostelini, three   genera and five species in Platymetopiini and 14 genera and 82 species in Scaphoideini). However, since 1967 many papers on Neotropical Deltocephalinae have been published including classification and nomenclatorial alterations, new taxa and geographical distribution. The complete bibliography of the leafhopper literature up to 1955 can be found in the General Catalogue of the Homoptera, Fascicle VI, Part 10 (METCALF, 1962-1968). OMAN et al. (1990) published a complete list of the world genera of Cicadellidae and the bibliography between 1955-1985. In this work are recorded 21 Neotropical subfamilies, 16 Neotropical tribes and 184 Neotropical genera (one genus in Acinopterini, one genus in Cicadullini, one genus in Cerrillini, six genera in Hecalini, one genus in Luheriini, two genera in  Doraturini, two genera in Stenometopiini, four genera in Scaphytopiini, two genera in Platymetopiini, six genera in Scaphoideini, one genus in Balcluthini, seven genera in Macrostelini, two genera in Opsiini, one genus in Penthimiini, 40 genera in Deltocephalini and 107 genera in Athysanini); eight genera without references about the tribe. Another subfamily and genus were added by GODOY & WEBB (1994). This catalogue is an attempt to offer the names and bibliographic references for taxa of Deltocephalinae (Caribbean, Central America and South America). After each species-group name, the type locality, and anabbreviation of the institution where the type is deposited, are given. The geographical distribution is based upon previously published records. Each species-group name is followed by the informations including of the author (s), publication year and page and when not strictly taxonomical, an abbreviated indication of the matter treated such as: cat. — catalogue, desc. — description, distr. — geographical distribution, ill. — illustration, rev. — revision, syn. — synonymy, tax. — taxonomy.


Zootaxa ◽  
2020 ◽  
Vol 4789 (2) ◽  
pp. 523-553
Author(s):  
MIGUEL A. MONNÉ ◽  
ANTONIO SANTOS-SILVA ◽  
MARCELA L. MONNÉ

A key for identification of the 45 genera of Acanthocinini with erect setae on the elytra and which occur in South America is provided. A new synonymy is proposed for Trichonyssodrys Gilmour, 1957 (junior synonym of Pentheochaetes Melzer, 1932), resulting in new combinations for the following species: Pentheochaetes aureopilosa (Monné, 1990), P. cincta (Delfino, 1981), P. maculata (Gilmour, 1957), P. melasma (Delfino, 1981), and P. nessimiani (Monné & Monné, 2012). The gender of the species-group names in Pentheochaetes is corrected. Diagnosis for each genus is provided, as well as type-locality and geographical distribution of the type-species. 


2019 ◽  
Vol 40 (1) ◽  
pp. 45-50
Author(s):  
Carlos R. Vilela ◽  
Gerhard Bächli

The male terminalia of a non-type Diathoneura longipennis (Malloch 1926) specimen,collected in Peru, were dissected and analyzed. The aedeagus and associated sclerites were found tohave been fixed at a late stage of protrusion, resulting in a different morphology, when compared to thetwo previous publications, which were fixed at earlier stages. Consequently, additional details of certainanatomical parts were observed and a better understanding of the aedeagus protruding process was attained.Diathoneura longipennis has been previously identified in San Mateo, Alajuela, Costa Rica (type locality)and Panama, and this specimen represents the first record of this species in South America.


Zootaxa ◽  
2012 ◽  
Vol 3373 (1) ◽  
pp. 1 ◽  
Author(s):  
HOUHUN LI ◽  
KLAUS SATTLER

The genus Mesophleps Hübner (Lepidoptera: Gelechiidae) is revised; 54 available names (including one unjustifiedemendation), one junior primary homonym and one unavailable name were considered; type material of 44 previouslydescribed nominal species was examined. Nine new species are described: M. acutunca sp. nov., M. bifidella sp. nov., M.unguella sp. nov., M. gigantella sp. nov., M. coffeae sp. nov., M. parvella sp. nov., M. aspina sp. nov., M. truncatella sp.nov. and M. undulatella sp. nov. Two possibly new species are discussed but not formally named for lack of material.Twenty-five new combinations are introduced: M. safranella (Legrand, 1965) comb. nov., M. epichorda (Turner, 1919)comb. nov., M. tabellata (Meyrick, 1913) comb. nov., M. crocina (Meyrick, 1904) comb. nov., M. ochracella (Turati,1926) comb. nov., M. geodes (Meyrick, 1929) comb. nov., M. catericta (Meyrick, 1927) comb. nov., M. tephrastis(Meyrick, 1904) comb. nov., M. cycnobathra (Lower, 1898) comb. nov., M. tetrachroa (Lower, 1898) comb. nov., M.ochroloma (Lower, 1901) comb. nov., M. trichombra (Lower, 1898) comb. nov., M. mylicotis (Meyrick, 1904) comb. nov.,M. macrosemus (Lower, 1900) comb. nov., M. apentheta (Turner, 1919) comb. nov., M. meliphanes (Lower, 1894) comb.nov., M. chloranthes (Lower, 1900) comb. nov., M. centrothetis (Meyrick, 1904) comb. nov., M. chloristis (Meyrick,1904) comb. nov., M. argonota (Lower, 1901) comb. nov., Megacraspedus arnaldi (Turati & Krüger, 1936) comb. nov.,Aponoea cinerellus (Turati, 1930) comb. nov., Pycnobathra acromelas (Turner, 1919) comb. nov., Sarotorna mesoleuca(Lower, 1900) comb. nov., S. dentata Meyrick, 1904, comb. nov. One species, Nothris mesophracta Turner, 1919, isremoved from Mesophleps but no current genus is available. Fourteen new synonymies (one genus, 13 species-group taxa)are established: Bucolarcha Meyrick, 1929, syn. nov. of Mesophleps Hübner, [1825]; Stiphrostola longinqua Meyrick,1923, syn. nov. and Brachyacma trychota Meyrick, 1929, syn. nov. of M. ioloncha (Meyrick, 1905); Lipatia crotalariellaBusck, 1910, syn. nov. of M. adustipennis (Walsingham, 1897); Brachyacma epichorda Turner, 1919, syn. nov. of M.epiochra (Meyrick, 1886); Mesophleps pudicellus var. apicellus Caradja, 1920, syn. nov. and Mesophleps silacellus subsp.calaritanus Amsel, 1939, syn. nov. of M. silacella (Hübner, 1796); Mesophleps lala Agenjo, [1961], syn. nov. of M.corsicella (Herrich-Schäffer, 1856); Crossobela barysphena Meyrick, 1923, syn. nov. of M. trinotella Herrich-Schäffer,1856; Mesophleps orientella Nel & Nel, 2003, syn. n. and Mesophleps gallicella Varenne & Nel, 2011, syn. nov. of M.ochracella (Turati, 1926); Nothris centrothetis Meyrick, 1904, syn. nov. and Nothris chloristis Meyrick, 1904, syn. nov.of M. chloranthes (Lower, 1900); Mesophleps cinerellus Turati, 1930, syn. nov. of Aponoea obtusipalpis Walsingham,1905. One genus and one species are recalled from synonymy: Pycnobathra Lower, 1901, gen. rev., and M. ioloncha(Meyrick, 1905) sp. rev. Lectotypes are designated, in accordance with the Code, article 74.7.3, for 14 species: Gelechiapalpigera Walsingham, 1891; Paraspistes ioloncha Meyrick, 1905; Lathontogenus adustipennis Walsingham, 1897;Brachyacma epichorda Turner, 1919; Nothris crocina Meyrick, 1904; Nothris ochracella Turati, 1926; Nothris tephrastisMeyrick, 1904; Ypsolophus ochroloma Lower, 1901; Ypsolophus macrosemus Lower, 1900; Nothris centrothetis Meyrick,1904; Nothris chloristis Meyrick, 1904; Ypsolophus argonota Lower, 1901; Mesophleps arnaldi Turati & Krüger, 1936,and Mesophleps cinerellus Turati, 1930. Mesophleps is a widely distributed Old World genus, except for one New Worldspecies, with seed-feeding larvae on Cupressaceae, Cistaceae, Cruciferae (Brassicaceae), Leguminosae (Fabaceae), Rubiaceae and doubtfully Dipterocarpaceae.


Zootaxa ◽  
2021 ◽  
Vol 4942 (4) ◽  
pp. 583-591
Author(s):  
FABIANO STEFANELLO

The giant water bug fauna from tropical South America remains poorly known. Three species of Belostoma Latreille (Belostoma fittkaui De Carlo, B. sayagoi De Carlo and B. hirsutum Roback & Nieser) have been cited only a few times in the literature. These three species are remarkable since they represent an extreme variation for the genus, with article II of the labium distinctly shorter than article III. Here, the synonymy of B. hirsutum with B. sayagoi is proposed based on examination of type material and additional specimens. Further, B. fittkaui and B. sayagoi are redescribed, including discussion about comparative morphology with congeners. A new species group is proposed for these species and a key to the Belostoma species groups is provided. Distribution records are also updated. 


2009 ◽  
Vol 99 (4) ◽  
pp. 431-436 ◽  
Author(s):  
Filipe A. C. do Nascimento ◽  
Marcelo G. de Lima ◽  
Gabriel O Skuk ◽  
Rafael O. de Sá

The tadpole of Hypsiboas atlanticus (Caramaschi & Velosa, 1996) is described from the municipality of Maceió, State of Alagoas, Brazil. At stage 36 the larvae have an overall elliptical body in lateral and dorsal views, oral disc anteroventral, spiracular tube sinistral, and labial tooth row formula 2(1,2)/3(1). The oral disc is surrounded, almost completely (anterior medial gap present) by a single row of marginal papillae. Described tadpoles of the H. punctatus species group can be differentiated by a combined disc oral features. Additional descriptions of H. punctatus (Schneider, 1799) tadpoles from populations throughout South America may be helpful in determining the status of these populations.


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. 


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