scholarly journals Human Q Fever on the Guiana Shield and Brazil: Recent Findings and Remaining Questions

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 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 Diaprepes abbreviatus (L.) (Col., Curculionidae) (Citrus Weevil). Host Plants: Citrus, cassava, maize, sugar cane. Information is given on the geographical distribution in NORTH AMERICA, USA, WEST INDIES, SOUTH AMERICA, French Guiana.


Author(s):  
J. M. Pérez

Abstract A description is provided for Leucocintractia scleriae. Information is included on the disease caused by the organism, its transmission, geographical distribution, and hosts. DISEASE: Development of spikelets is prevented in infected plants. HOSTS: Rhynchospora corymbosa, R. gigantea and R. triflora (Cyperaceae). GEOGRAPHICAL DISTRIBUTION: AFRICA: Congo, Zaire. NORTH AMERICA: Mexico. CENTRAL AMERICA: Costa Rica, Cuba, Honduras, Puerto Rico. SOUTH AMERICA: Colombia, French Guiana, Guyana [as British Guiana], Paraguay, Venezuela. ASIA: China (Taipei), India, Indonesia, Singapore, Taiwan. AUSTRALASIA: Australia (Queensland). TRANSMISSION: Not studied; probably by teliospores dispersed by wind and water.


Zootaxa ◽  
2020 ◽  
Vol 4806 (1) ◽  
pp. 1-144
Author(s):  
STEFFEN BAYER ◽  
HUBERT HÖFER ◽  
HEIKO METZNER

We propose a revision of the spider genus Corythalia C.L. Koch, 1850 (Salticidae: Euophryini) with a revised genus diagnosis based on examination of all species available to us. In this paper we redescribe all previously described species from South America with revised species diagnoses and describe 20 new species from South America (and the nearby islands). For C. latipes, the type species of the genus Corythalia, a neotype is designated. In total, 52 nominal species of the genus are herein treated, 46 species are recognized as valid. The females of C. waleckii Taczanowski, 1871, C. luctuosa Caporiacco, 1954 and C. latipes (C.L. Koch, 1846) are described for the first time. Corythalia sellata Simon, 1901, erroneously considered as nomen nudum in the present version of the World Spider Catalog, is here recognised as a valid species. Corythalia fulgipedia Crane, 1948 is also considered a valid species and is removed from the synonymy of C. tropica (Mello-Leitão, 1939). One name is considered a nomen dubium (Corythalia variegata Caporiacco, 1954), two are nomina nuda (C. major Simon, 1901; C. dimidiata Simon, 1901). Two species are transferred to other genera: C. argyrochrysos (Mello-Leitão, 1946) to Pachomius Peckham & Peckham, 1896 as Pachomius argyrochrysos (Mello-Leitão, 1946), comb. nov. and C. heliophanina (Taczanowski, 1871) to Neonella Gertsch, 1936, as Neonella heliophanina (Taczanowski, 1871), comb. nov. under incertae sedis. One species is synonymised: C. barbipes (Mello-Leitão, 1939) is a junior synonym of C. cincta (Badcock, 1932), syn. nov. The new Corythalia species are: C. conferta sp. nov. (♂♀, Brazil), C. concinna sp. nov. (♀, Brazil), C. drepane sp. nov. (♂♀, Brazil), C. drepanopsis sp. nov. (♀, Brazil), C. antepagmenti sp. nov. (♂♀, Brazil), C. ricti Bayer, sp. nov. (♂, Guyana), C. protensa sp. nov. (♂, Brazil), C. gasnieri sp. nov. (♂, Brazil), C. verhaaghi sp. nov. (♀, Brazil), C. scutellaris Bayer, sp. nov. (♂♀, Ecuador), C. dakryodes Bayer, sp. nov. (♀, Colombia), C. foelixi Bayer, sp. nov. (♂♀, French Guiana), C. longiducta sp. nov. (♀, Brazil), C. latior sp. nov. (♂, Bolivia), C. trochophora Bayer, sp. nov. (♂, Ecuador), C. lineata Bayer, sp. nov. (♂, Guyana), C. hamulifera Bayer, sp. nov. (♂, Ecuador), C. tribulosa sp. nov. (♂, Colombia), C. flagrans sp. nov. (♂, Brazil) and C. fragilis sp. nov. (♂♀, Brazil). Illustrations are provided for all of the new species and for all (primary) type specimens of the species re-described. Hypotheses of possible relationships among the different species of Corythalia are discussed. 


2017 ◽  
Vol 47 (2) ◽  
pp. 95-102
Author(s):  
Rodrigo Schütz RODRIGUES

ABSTRACT Rapateaceae is a monocot family centered in the Guiana Shield region of South America. This article reports four generic additions to the Rapateaceae of Rondônia, a state in northern Brazil. Cephalostemon gracilis (Poepp. & Endl.) R.H.Schomb., Duckea cyperaceoidea (Ducke) Maguire, Monotrema xyridoides Gleason, and Schoenocephalium cucullatum Maguire were recorded in lowland savannas and open white-sand ecosystems in the state. These findings extend significantly the known diversity of the Rapateaceae taxa occurring in Rondônia, and represent an extension of their geographical distribution to a Brazilian state with no part of its territory in the Guiana Shield.


1994 ◽  
Vol 5 (3) ◽  
pp. 113-118 ◽  
Author(s):  
Monique Goyette ◽  
André Poirier ◽  
Jean Bouchard ◽  
Eric Morrier

Q fever, a zoonosis acquired by inhalation of the rickettsiaCoxiella burnetii, is rarely diagnosed in Canada. The world incidence has been increasing since 1960, because of progressive dissemination of this microorganism in animal populations, particularly domestic ruminants. Some recent outbreaks were caused by cats. Of 14 cases reported in Quebec between 1989 and the beginning of 1993, nine occurred successively in an 18-month period in the rural region surrounding Trois-Rivières, after contact with livestock or cats. These cases are reported here, with the results of serological screening of the workers of an abattoir where one of the cases worked. Five additional cases reported in Quebec during the same period are briefly reviewed.


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.


Check List ◽  
2020 ◽  
Vol 16 (2) ◽  
pp. 387-390
Author(s):  
Eudi Bonfim do Nascimento ◽  
Éder dos Santos Souza ◽  
Vinicius Fernandes de Paiva ◽  
Érica Cristina da Silva Chagas ◽  
Cleber Galvão

Cavernicola pilosa Barber, 1937 is a wild triatomine species that generally lives in caves but has been found invading dwellings. It feeds mostly on bat blood. This vector has a wide geographical distribution throughout Central and South America, including Brazil, Ecuador, Colombia, French Guiana, Panamá, Peru, and Venezuela. In Brazil, C. pilosa occurs in the states of Bahia, Pará, Tocantins, Espírito Santo, Goiás, Mato Grosso do Sul, Minas Gerais, Paraná, and Maranhão. We report for the first time its presence in Amazonas state, Brazil. 


Author(s):  

Abstract A new distribution map is provided for Meloidogyne hispanica Hirschmann. Secernentea: Tylenchida: Meloidogynidae. Hosts: polyphagous. Information is given on the geographical distribution in Europe (Greece, Portugal, Spain), Asia (China, Hainan, Iran), Africa (Burkina Faso, Malawi, South Africa), Central America & Caribbean (Costa Rica, Guadeloupe, Martinique), South America (Brazil, Bahia, Pernambuco, French Guiana), Oceania (Australia).


Author(s):  

Abstract A new distribution map is provided for Bactrocera carambolae Drew & Hancock Diptera: Tephritidae carambola fly. Attacks a wide range of fruits particularly carambola (Averrhoa carambola). Information is given on the geographical distribution in ASIA, Andaman Islands, Brunei, Indonesia, Java, Lombok, Sumbawa, Malaysia, Sabah, Peninsular Malaysia, Singapore, Thailand, SOUTH AMERICA, French Guiana, Guyana, Surinam.


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