scholarly journals Catálogo dos Deltocephalinae (Hemiptera: Cicadellidae) neotropicais (incluíndo o norte do México). Parte I — Athysanini e Deltocephalini excluídos

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. 


2020 ◽  
Vol 28 (2) ◽  
pp. 108-142
Author(s):  
Charlotte M. Taylor ◽  
Jomar G. Jardim

Review of specimens and names of Faramea Aubl. (Rubiaceae, Coussareeae) has required new nomenclatural combinations, clarified the identities of some previously described species, and discovered some new taxa. Here we transfer two Faramea names, F. suaveolens Duchass. and F. panurensis Müll. Arg., to Coussarea Aubl.; review the identities of F. cuencana Standl., F. multiflora A. Rich., F. oblongifolia Standl., F. parvibractea Steyerm., F. spathacea Müll. Arg. ex Standl., and F. suerrensis (Donn. Sm.) Donn. Sm.; lectotypify F. multiflora and F. panurensis; transfer to Faramea and lectotypify Rudgea scandens K. Krause; and describe 13 new species and two new subspecies: F. camposiana C. M. Taylor of Ecuador and Peru, F. foreroana C. M. Taylor of Colombia, F. fosteri C. M. Taylor of western South America, F. galerasana C. M. Taylor of Ecuador, F. grayumiana C. M. Taylor of Central America, F. kampauicola C. M. Taylor of Ecuador and Peru, F. neilliana C. M. Taylor of western South America, F. premontana C. M. Taylor of Ecuador, F. quijosana C. M. Taylor of Ecuador, F. ramosiana C. M. Taylor of Colombia, F. reyneliana C. M. Taylor of Peru, F. stoneana C. M. Taylor with two subspecies from Central and western South America, F. suerrensis subsp. miryamiae C. M. Taylor from Colombia, and F. vernicosa C. M. Taylor of Ecuador and Peru.


Author(s):  
Loïc Epelboin ◽  
Carole Eldin ◽  
Pauline Thill ◽  
Vincent Pommier de Santi ◽  
Philippe Abboud ◽  
...  

Abstract Purpose of Review In this review, we report on the state of knowledge about human Q fever in Brazil and on the Guiana Shield, an Amazonian region located in northeastern South America. There is a contrast between French Guiana, where the incidence of this disease is the highest in the world, and other countries where this disease is practically non-existent. Recent Findings Recent findings are essentially in French Guiana where a unique strain MST17 has been identified; it is probably more virulent than those usually found with a particularly marked pulmonary tropism, a mysterious animal reservoir, a geographical distribution that raises questions. Summary Q fever is a bacterial zoonosis due to Coxiella burnetii that has been reported worldwide. On the Guiana Shield, a region mostly covered by Amazonian forest, which encompasses the Venezuelan State of Bolivar, Guyana, Suriname, French Guiana, and the Brazilian State of Amapá, the situation is very heterogeneous. While French Guiana is the region reporting the highest incidence of this disease in the world, with a single infecting clone (MST 117) and a unique epidemiological cycle, it has hardly ever been reported in other countries in the region. This absence of cases raises many questions and is probably due to massive under-diagnosis. Studies should estimate comprehensively the true burden of this disease in the region.


Author(s):  

Abstract A new distribution map is provided for Phaeoisariopsis bataticola (Cif. & Bruner) M.B. Ellis. Host: sweet potato (Ipomoea spp.). Information is given on the geographical distribution in NORTH AMERICA, USA, Florida, CENTRAL AMERICA & WEST INDIES, Cuba, Dominican Republic, Puerto Rico, SOUTH AMERICA, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Spiroplasma kunkelii Whitcomb, Chen et al. Bacteria. Hosts: maize (Zea mays), sweetcorn (Zea mays subsp. mays), teosinte (Zea mexicana) and perennial teosinte (Zea perennis). Information is given on the geographical distribution in North America (Mexico, USA, California, Florida, Louisiana, Michigan, Mississippi, Ohio, Texas), Central America and Caribbean (Belize, El Salvador, Guatemala, Honduras, Jamaica, Nicaragua, Panama), South America (Argentina, Bolivia, Brazil, Mato Grosso do Sul, Minas Gerais, Colombia, Paraguay, Peru, Venezuela).


Author(s):  

Abstract A new distribution map is provided for Phomopsis elaeidis Punith. Hosts: oil palm (Elaeis guineensis). Information is given on the geographical distribution in AFRICA, Guinea, Nigeria, Tanzania, Zaire, ASIA, Malaysia, E. Malaysia, India, AUSTRALASIA & OCEANIA, Australia, NT, Solomon Islands, CENTRAL AMERICA, Dominica, SOUTH AMERICA, Ecuador.


Author(s):  

Abstract A new distribution map is provided for Epitrix fasciata Blatchley (Epitrix parvula(F.)) (Col., Chrysomelidae). Host Plants: Potato, tobacco, tomato, brinjal. Information is given on the geographical distribution in PACIFIC ISLANDS, Hawaii, Society Islands, NORTH AMERICA, Mexico, USA, CENTRAL AMERICA and WEST INDIES, SOUTH AMERICA, Argentina, Brazil, Colombia, Guyana, Surinam, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Typophorus nigritus (Fabricius) Coleoptera: Chrysomelidae, Eumolpinae. Attacks sweet-potato. Information is given on the geographical distribution in CENTRAL AMERICA and CARIBBEAN, Costa Rica, Cuba, Grenada, Grenadine Islands, Guatemala, Honduras, Mexico, Nicaragua, Panama, St. Vincent, Trinidad, SOUTH AMERICA, Argentina, Bolivia, Brazil, Colombia, Equador, French Guiana, Guyana, Paraguay, Peru, Uruguay, Venezuela.


Author(s):  

Abstract A new distribution map is provided for Alabama argillacea (Hb.) (Cotton Leafworm). Hosts: Cultivated and wild cottons (Gossypium spp.), Thespesia populnea. Information is given on the geographical distribution in NORTH AMERICA, Canada, Mexico, U.S.A., CENTRAL AMERICA and WEST INDIES, Guatemala, Nicaragua, Salvador, West Indies, SOUTH AMERICA, Argentina, Brazil, British Guiana, Colombia, Dutch Guiana, Ecuador, Paraguay, Peru, Venezuela.


Author(s):  
J. M. Pérez

Abstract A description is provided for Sporisorium paspali-notati. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: Spikelet development is prevented in infected plants. HOSTS: Paspalum dilatatum, P. notatum, P. plicatulum, P. proliferum, P. urvillei and P. vaginatum (Poaceae). GEOGRAPHICAL DISTRIBUTION: NORTH AMERICA: Mexico. CENTRAL AMERICA: Cuba, Trinidad & Tobago. SOUTH AMERICA: Brazil. TRANSMISSION: Probably by air-borne teliospores. Wind is the most common dispersal mode of smut teliospores.


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