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Registro completo
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Biblioteca (s) : |
INIA Las Brujas. |
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Fecha : |
21/02/2014 |
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Actualizado : |
22/02/2014 |
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Autor : |
Johnson, R.T. ; Alexander, J.T. ; Rush, G.E. ; Hawkes, G.R. |
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Título : |
Advances in sugarbeet production : principles and practices |
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Fecha de publicación : |
1971 |
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Fuente / Imprenta : |
Iowa (USA): Iowa State University, 1971. |
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Páginas : |
470p. |
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ISBN : |
ISBN 0-8138-1415-4 |
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Idioma : |
Español |
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Thesagro : |
ABONOS FOSFATADOS; ABONOS NITROGENADOS; ABONOS POTASICOS; ABSORCION DE SUSTANCIAS NUTRITIVAS; BETA VULGARIS; CONTROL DE ENFERMEDADES; CONTROL DE INSECTOS; CONTROL DE NEMATODOS; COSECHA; ENFERMEDADES DE LAS PLANTAS; ESCARDA; FACTORES AMBIENTALES; INSECTOS DAÑINOS; OLIGOELEMENTOS; ORDENACION DE AGUAS; ORDENACION DE CULTIVOS; PLANTAS AZUCARERAS; PRODUCCION; PRODUCCION DE SEMILLAS; REMOLACHA AZUCARERA; RIEGO; TRATAMIENTO PRECOSECHA; VARIEDADES. |
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Asunto categoría : |
-- |
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Marc : |
LEADER 01184nam a2200421 a 4500
001 1000143
005 2014-02-22
008 1971 bl uuuu u00u1 u #d
100 1 $aJOHNSON, R.T.
245 $aAdvances in sugarbeet production$bprinciples and practices
260 $aIowa (USA): Iowa State University$c1971
300 $a470p.
650 $aABONOS FOSFATADOS
650 $aABONOS NITROGENADOS
650 $aABONOS POTASICOS
650 $aABSORCION DE SUSTANCIAS NUTRITIVAS
650 $aBETA VULGARIS
650 $aCONTROL DE ENFERMEDADES
650 $aCONTROL DE INSECTOS
650 $aCONTROL DE NEMATODOS
650 $aCOSECHA
650 $aENFERMEDADES DE LAS PLANTAS
650 $aESCARDA
650 $aFACTORES AMBIENTALES
650 $aINSECTOS DAÑINOS
650 $aOLIGOELEMENTOS
650 $aORDENACION DE AGUAS
650 $aORDENACION DE CULTIVOS
650 $aPLANTAS AZUCARERAS
650 $aPRODUCCION
650 $aPRODUCCION DE SEMILLAS
650 $aREMOLACHA AZUCARERA
650 $aRIEGO
650 $aTRATAMIENTO PRECOSECHA
650 $aVARIEDADES
700 1 $aALEXANDER, J.T.
700 1 $aRUSH, G.E.
700 1 $aHAWKES, G.R.
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Registro original : |
INIA Las Brujas (LB) |
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 | Acceso al texto completo restringido a Biblioteca INIA Tacuarembó. Por información adicional contacte bibliotb@tb.inia.org.uy. |
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Registro completo
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Biblioteca (s) : |
INIA Tacuarembó. |
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Fecha actual : |
21/02/2014 |
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Actualizado : |
01/10/2019 |
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Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
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Circulación / Nivel : |
Internacional - -- |
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Autor : |
STEWART, J.E.; ROSS-DAVIS, A.L.; GRAÇA, R.N.; ALFENAS, A.C.; PEEVER, T.L.; HANNA, J.W.; UCHIDA, J.Y.; HAUFF, R.D.; KADOOKA, C.Y.; KIM, M.S.; CANNON, P.G.; NAMBA, S.; SIMETO, S.; PÉREZ, C.A.; RAYMAJHI, M.B.; LODGE, D.J.; ARGUEDAS, M.; MEDEL-ORTIZ, R.; LÓPEZ-RAMIREZ, M.A.; TENNANT, P.; GLEN, M.; MACHADO, P.S.; MCTAGGART, A.R.; CARNEGIE, A.J.; KLOPFENTEIN, N.B. |
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Afiliación : |
1Department of Bioagricultural Science and Pest Management, Colorado State University, USA.; USDA Forest Service, Rocky Mountain Research Station, Moscow Forestry Sciences Laboratory, USA.; FuturaGene Brasil Tecnologia Ltda, Brazil.; Department of Plant Pathology, Universidade Federal de Viçosa, Brazil.; Department of Plant Pathology, Washington State University, USA.; USDA Forest Service, Rocky Mountain Research Station, Moscow Forestry Sciences Laboratory, USA.; Department of Plant and Environmental Protection Sciences, University of Hawaii at Manoa, USA.; Division of Forestry and Wildlife, Department of Lands and Natural Resources, Honolulu, USA.; Department of Plant and Environmental Protection Sciences, University of Hawaii at Manoa, Honolulu, USA.; Department of Forestry, Environment and Systems, Kookmin University, Seoul, South Korea.; USDA Forest Service, Forest Health Protection, USA.; Department of Agricultural and Environmental Biology, The University of Tokyo, Japan.; SOFIA SIMETO FERRARI, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; Departamento de Protección Vegetal, EEMAC, Facultad de Agronomía, Universidad de la República, Paysandú, Uruguay.; USDA, Agricultural Research Service, Invasive Plant Research Laboratory, Fort Lauderdale, FL, USA.; USDA Forest Service, Northern Research Station, Luquillo, Puerto Rico.; Escuela de Ingeniería Forestal, Instituto Tecnológico de Costa Rica, Cartago, Costa Rica.; Instituto de Investigaciones Forestales, Universidad Veracruzana, Xalapa, Mexico.; Instituto de Investigaciones Forestales, Universidad Veracruzana, Xalapa, Mexico.; The Biotechnology Centre, University of the West Indies, Mona, Jamaica.; Tasmanian Institute of Agriculture, University of Tasmania, Hobart, Australia.; Department of Plant Pathology, Universidade Federal de Viçosa, Brazil.; Queensland Alliance for Agriculture and Food Innovation, The University of Queensland, Brisbane, Australia.; NSW Department of Primary Industries, NSW Forest Science, Parramatta, Australia.; USDA Forest Service, Rocky Mountain Research Station, Moscow Forestry Sciences Laboratory, Moscow, USA. |
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Título : |
Genetic diversity of the myrtle rust pathogen (Austropuccinia psidii) in the Americas and Hawaii: Global implications for invasive threat assessments. |
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Fecha de publicación : |
2017 |
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Fuente / Imprenta : |
Forest Pathology, v. 48, no. 1, 2017. |
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DOI : |
10.1111/efp.12378 |
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Idioma : |
Inglés |
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Notas : |
Article history: Received: 14 February 2017 // Accepted: 3 August 2017. |
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Contenido : |
Since the myrtle rust pathogen (Austropuccinia psidii) was first reported (as Puccinia psidii) in Brazil on guava (Psidium guajava) in 1884, it has been found infecting diverse myrtaceous species. Because A. psidii has recently spread rapidly worldwide with an extensive host range, genetic and genotypic diversities were evaluated within and among A. psidii populations in its putative native range and other areas of myrtle rust emergence in the Americas and Hawaii. Microsatellite markers revealed several unique multilocus genotypes (MLGs), which grouped isolates into nine distinct genetic clusters [C1?C9 comprising C1: from diverse hosts from Costa Rica, Jamaica, Mexico, Puerto Rico, and USA-Hawaii, and USA-California; C2: from eucalypts (Eucalyptus spp.) in Brazil/Uruguay and rose apple (Syzygium jambos) in Brazil; C3: from eucalypts in Brazil; C4: from diverse hosts in USA-Florida; C5: from Java plum (Syzygium cumini) in Brazil; C6: from guava and Brazilian guava (Psidium guineense) in Brazil; C7: from pitanga (Eugenia uniflora) in Brazil; C8: from allspice (Pimenta dioica) in Jamaica and sweet flower (Myrrhinium atropurpureum) in Uruguay; C9: from jabuticaba (Myrciaria cauliflora) in Brazil]. The C1 cluster, which included a single MLG infecting diverse host in many geographic regions, and the closely related C4 cluster are considered as a ?Pandemic biotype,? associated with myrtle rust emergence in Central America, the Caribbean, USA-Florida, USA-Hawaii, Australia, China-Hainan, New Caledonia, Indonesia and Colombia. Based on 19 bioclimatic variables and documented occurrences of A. psidii contrasted with reduced sets of specific genetic clusters (subnetworks, considered as biotypes), maximum entropy bioclimatic modelling was used to predict geographic locations with suitable climate for A. psidii which are at risk from invasion. The genetic diversity of A. psidii throughout the Americas and Hawaii demonstrates the importance of recognizing biotypes when assessing the invasive threats posed by A. psidii around the globe. MenosSince the myrtle rust pathogen (Austropuccinia psidii) was first reported (as Puccinia psidii) in Brazil on guava (Psidium guajava) in 1884, it has been found infecting diverse myrtaceous species. Because A. psidii has recently spread rapidly worldwide with an extensive host range, genetic and genotypic diversities were evaluated within and among A. psidii populations in its putative native range and other areas of myrtle rust emergence in the Americas and Hawaii. Microsatellite markers revealed several unique multilocus genotypes (MLGs), which grouped isolates into nine distinct genetic clusters [C1?C9 comprising C1: from diverse hosts from Costa Rica, Jamaica, Mexico, Puerto Rico, and USA-Hawaii, and USA-California; C2: from eucalypts (Eucalyptus spp.) in Brazil/Uruguay and rose apple (Syzygium jambos) in Brazil; C3: from eucalypts in Brazil; C4: from diverse hosts in USA-Florida; C5: from Java plum (Syzygium cumini) in Brazil; C6: from guava and Brazilian guava (Psidium guineense) in Brazil; C7: from pitanga (Eugenia uniflora) in Brazil; C8: from allspice (Pimenta dioica) in Jamaica and sweet flower (Myrrhinium atropurpureum) in Uruguay; C9: from jabuticaba (Myrciaria cauliflora) in Brazil]. The C1 cluster, which included a single MLG infecting diverse host in many geographic regions, and the closely related C4 cluster are considered as a ?Pandemic biotype,? associated with myrtle rust emergence in Central America, the Caribbean, USA-Florida, USA-Hawaii, Australia, China-... Presentar Todo |
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Thesagro : |
PATOLOGIA FORESTAL. |
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Asunto categoría : |
H20 Enfermedades de las plantas |
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Marc : |
LEADER 03365naa a2200445 a 4500
001 1028016
005 2019-10-01
008 2017 bl uuuu u00u1 u #d
024 7 $a10.1111/efp.12378$2DOI
100 1 $aSTEWART, J.E.
245 $aGenetic diversity of the myrtle rust pathogen (Austropuccinia psidii) in the Americas and Hawaii$bGlobal implications for invasive threat assessments.$h[electronic resource]
260 $c2017
500 $aArticle history: Received: 14 February 2017 // Accepted: 3 August 2017.
520 $aSince the myrtle rust pathogen (Austropuccinia psidii) was first reported (as Puccinia psidii) in Brazil on guava (Psidium guajava) in 1884, it has been found infecting diverse myrtaceous species. Because A. psidii has recently spread rapidly worldwide with an extensive host range, genetic and genotypic diversities were evaluated within and among A. psidii populations in its putative native range and other areas of myrtle rust emergence in the Americas and Hawaii. Microsatellite markers revealed several unique multilocus genotypes (MLGs), which grouped isolates into nine distinct genetic clusters [C1?C9 comprising C1: from diverse hosts from Costa Rica, Jamaica, Mexico, Puerto Rico, and USA-Hawaii, and USA-California; C2: from eucalypts (Eucalyptus spp.) in Brazil/Uruguay and rose apple (Syzygium jambos) in Brazil; C3: from eucalypts in Brazil; C4: from diverse hosts in USA-Florida; C5: from Java plum (Syzygium cumini) in Brazil; C6: from guava and Brazilian guava (Psidium guineense) in Brazil; C7: from pitanga (Eugenia uniflora) in Brazil; C8: from allspice (Pimenta dioica) in Jamaica and sweet flower (Myrrhinium atropurpureum) in Uruguay; C9: from jabuticaba (Myrciaria cauliflora) in Brazil]. The C1 cluster, which included a single MLG infecting diverse host in many geographic regions, and the closely related C4 cluster are considered as a ?Pandemic biotype,? associated with myrtle rust emergence in Central America, the Caribbean, USA-Florida, USA-Hawaii, Australia, China-Hainan, New Caledonia, Indonesia and Colombia. Based on 19 bioclimatic variables and documented occurrences of A. psidii contrasted with reduced sets of specific genetic clusters (subnetworks, considered as biotypes), maximum entropy bioclimatic modelling was used to predict geographic locations with suitable climate for A. psidii which are at risk from invasion. The genetic diversity of A. psidii throughout the Americas and Hawaii demonstrates the importance of recognizing biotypes when assessing the invasive threats posed by A. psidii around the globe.
650 $aPATOLOGIA FORESTAL
700 1 $aROSS-DAVIS, A.L.
700 1 $aGRAÇA, R.N.
700 1 $aALFENAS, A.C.
700 1 $aPEEVER, T.L.
700 1 $aHANNA, J.W.
700 1 $aUCHIDA, J.Y.
700 1 $aHAUFF, R.D.
700 1 $aKADOOKA, C.Y.
700 1 $aKIM, M.S.
700 1 $aCANNON, P.G.
700 1 $aNAMBA, S.
700 1 $aSIMETO, S.
700 1 $aPÉREZ, C.A.
700 1 $aRAYMAJHI, M.B.
700 1 $aLODGE, D.J.
700 1 $aARGUEDAS, M.
700 1 $aMEDEL-ORTIZ, R.
700 1 $aLÓPEZ-RAMIREZ, M.A.
700 1 $aTENNANT, P.
700 1 $aGLEN, M.
700 1 $aMACHADO, P.S.
700 1 $aMCTAGGART, A.R.
700 1 $aCARNEGIE, A.J.
700 1 $aKLOPFENTEIN, N.B.
773 $tForest Pathology$gv. 48, no. 1, 2017.
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