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Biblioteca(s): |
Biblioteca Rui Tendinha. |
Data corrente: |
20/12/2016 |
Data da última atualização: |
20/12/2016 |
Autoria: |
MENEZES SOBRINHO, J. A. de (Org.). |
Título: |
Cultivo do alho (Allium sativum). |
Edição: |
3. ed. rev. amp. |
Ano de publicação: |
1997 |
Fonte/Imprenta: |
Brasília, DF : EMBRAPA-CNPH, 1997. |
Páginas: |
23 p. |
Série: |
(EMBRAPA-CNPH. Instruções Técnicas da Embrapa Hortaliças, 2). |
Idioma: |
Português |
Conteúdo: |
Exigências climáticas. Preparo do solo e calagem. Adubação. Deficiências nutricionais. Cultivares e épocas de plantio. Plantio. Cobertura morta. Irrigação. Manejo de plantas daninhas. Doenças. Ferrugem. Mancha-púrpura ou queima-das-folhas. Podridão-branca. Mofo-azul. Queima-bacteriana. Advertência quanto ao controle químico. Nematóides. Pragas. Tripes. Ácaro do bulbo. Traças. Pragas secundárias. Recomendações gerais sobre o uso de agrotóxicos e segurança de aplicação. Colheita. Armazenamento e cura. Classificação e comercialização. Coeficientes técnicos para cálculo do custo de produção (para 1 ha). |
Palavras-Chave: |
Adubação; Agrotóxico; Alho; Allium sativum; Armazenamento; Brasil; Calagem; Centro Nacional de Pesquisa de Hortali?as(Brasilia; Clima; Cobertura morta; Colheita; Comercialização; Cropping systems; Cultivation; Cultivo; Custo de produção; DF); Doença de planta; EMBRAPA; Erva daninha; Farming systems; Garlic; Gerlic; Irrigação; Plantio; Praga de planta; Producao; Sistema de produ?Æo; Sistema de producao; Solo; Variedade. |
Categoria do assunto: |
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Marc: |
LEADER 01964nam a2200517 a 4500 001 1013741 005 2016-12-20 008 1997 bl uuuu u0uu1 u #d 100 1 $aMENEZES SOBRINHO, J. A. de (Org.). 245 $aCultivo do alho (Allium sativum). 250 $a3. ed. rev. amp. 260 $aBrasília, DF : EMBRAPA-CNPH$c1997 300 $a23 p. 490 $a(EMBRAPA-CNPH. Instruções Técnicas da Embrapa Hortaliças, 2). 520 $aExigências climáticas. Preparo do solo e calagem. Adubação. Deficiências nutricionais. Cultivares e épocas de plantio. Plantio. Cobertura morta. Irrigação. Manejo de plantas daninhas. Doenças. Ferrugem. Mancha-púrpura ou queima-das-folhas. Podridão-branca. Mofo-azul. Queima-bacteriana. Advertência quanto ao controle químico. Nematóides. Pragas. Tripes. Ácaro do bulbo. Traças. Pragas secundárias. Recomendações gerais sobre o uso de agrotóxicos e segurança de aplicação. Colheita. Armazenamento e cura. Classificação e comercialização. Coeficientes técnicos para cálculo do custo de produção (para 1 ha). 653 $aAdubação 653 $aAgrotóxico 653 $aAlho 653 $aAllium sativum 653 $aArmazenamento 653 $aBrasil 653 $aCalagem 653 $aCentro Nacional de Pesquisa de Hortali?as(Brasilia 653 $aClima 653 $aCobertura morta 653 $aColheita 653 $aComercialização 653 $aCropping systems 653 $aCultivation 653 $aCultivo 653 $aCusto de produção 653 $aDF) 653 $aDoença de planta 653 $aEMBRAPA 653 $aErva daninha 653 $aFarming systems 653 $aGarlic 653 $aGerlic 653 $aIrrigação 653 $aPlantio 653 $aPraga de planta 653 $aProducao 653 $aSistema de produ?Æo 653 $aSistema de producao 653 $aSolo 653 $aVariedade
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Biblioteca Rui Tendinha (BRT) |
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| Acesso ao texto completo restrito à biblioteca da Biblioteca Rui Tendinha. Para informações adicionais entre em contato com biblioteca@incaper.es.gov.br. |
Registro Completo |
Biblioteca(s): |
Biblioteca Rui Tendinha. |
Data corrente: |
13/01/2015 |
Data da última atualização: |
13/01/2015 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 1 |
Autoria: |
MARRACCINI, P.; VINECKY, F.; ALVES, G. S. C.; RAMOS, H. J. O.; ELBELT, S.; VIEIRA, N. G.; CARNEIRO, F. A.; SUJII, P. S.; ALEKCEVETCH, J. C.; SILVA, V. A.; DaMATTA, F. M.; FERRÃO, M. A. G.; LEROY, T.; POT, D.; VIEIRA, L. G. E.; SILVA, F. R. da; ANDRADE, A. C. |
Afiliação: |
Maria Amélia Gava Ferrão, Incaper/Embrapa Café. |
Título: |
Differentially expressed genes and proteins upon drought acclimation in tolerant and sensitive genotypes of Coffea canephora. |
Ano de publicação: |
2012 |
Fonte/Imprenta: |
Journal of Experimental Botany, Oxford v. 63, n. 11, p. 4191-4212, 2012. |
Idioma: |
Inglês |
Conteúdo: |
The aim of this study was to investigate the molecular mechanisms underlying drought acclimation in coffee plants by the identification of candidate genes (CGs) using different approaches. The first approach used the data generated during the Brazilian Coffee expressed sequence tag (EST) project to select 13 CGs by an in silico analysis (electronic northern). The second approach was based on screening macroarrays spotted with plasmid DNA (coffee ESTs) with separate hybridizations using leaf cDNA probes from drought-tolerant and susceptible clones of Coffea canephora var. Conilon, grown under different water regimes. This allowed the isolation of seven additional CGs. The third approach used two-dimensional gel electrophoresis to identify proteins displaying differential accumulation in leaves of drought-tolerant and susceptible clones of C. canephora. Six of them were characterized by MALDI-TOF-MS/MS (matrix-assisted laser desorption-time of flight-tandem mass spectrometry) and the corresponding proteins were identified. Finally, additional CGs were selected from the literature, and quantitative real-time polymerase chain reaction (qPCR) was performed to analyse the expression of all identified CGs. Altogether, >40 genes presenting differential gene expression during drought acclimation were identified, some of them showing different expression profiles between drought-tolerant and susceptible clones. Based on the obtained results, it can be concluded that factors involved a complex network of responses probably involving the abscisic signalling pathway and nitric oxide are major molecular determinants that might explain the better efficiency in controlling stomata closure and transpiration displayed by drought-tolerant clones of C. canephora. MenosThe aim of this study was to investigate the molecular mechanisms underlying drought acclimation in coffee plants by the identification of candidate genes (CGs) using different approaches. The first approach used the data generated during the Brazilian Coffee expressed sequence tag (EST) project to select 13 CGs by an in silico analysis (electronic northern). The second approach was based on screening macroarrays spotted with plasmid DNA (coffee ESTs) with separate hybridizations using leaf cDNA probes from drought-tolerant and susceptible clones of Coffea canephora var. Conilon, grown under different water regimes. This allowed the isolation of seven additional CGs. The third approach used two-dimensional gel electrophoresis to identify proteins displaying differential accumulation in leaves of drought-tolerant and susceptible clones of C. canephora. Six of them were characterized by MALDI-TOF-MS/MS (matrix-assisted laser desorption-time of flight-tandem mass spectrometry) and the corresponding proteins were identified. Finally, additional CGs were selected from the literature, and quantitative real-time polymerase chain reaction (qPCR) was performed to analyse the expression of all identified CGs. Altogether, >40 genes presenting differential gene expression during drought acclimation were identified, some of them showing different expression profiles between drought-tolerant and susceptible clones. Based on the obtained results, it can be concluded that factors involved a... Mostrar Tudo |
Palavras-Chave: |
Candidate gene; Coffea canephora; Differential expression; Drought acclimation; Genética; Proteomic; Proteômica; Real time PCR. |
Thesagro: |
Café; Coffea canephora; Genetics. |
Categoria do assunto: |
-- |
Marc: |
LEADER 03034naa a2200445 a 4500 001 1004907 005 2015-01-13 008 2012 bl uuuu u00u1 u #d 100 1 $aMARRACCINI, P. 245 $aDifferentially expressed genes and proteins upon drought acclimation in tolerant and sensitive genotypes of Coffea canephora.$h[electronic resource] 260 $c2012 520 $aThe aim of this study was to investigate the molecular mechanisms underlying drought acclimation in coffee plants by the identification of candidate genes (CGs) using different approaches. The first approach used the data generated during the Brazilian Coffee expressed sequence tag (EST) project to select 13 CGs by an in silico analysis (electronic northern). The second approach was based on screening macroarrays spotted with plasmid DNA (coffee ESTs) with separate hybridizations using leaf cDNA probes from drought-tolerant and susceptible clones of Coffea canephora var. Conilon, grown under different water regimes. This allowed the isolation of seven additional CGs. The third approach used two-dimensional gel electrophoresis to identify proteins displaying differential accumulation in leaves of drought-tolerant and susceptible clones of C. canephora. Six of them were characterized by MALDI-TOF-MS/MS (matrix-assisted laser desorption-time of flight-tandem mass spectrometry) and the corresponding proteins were identified. Finally, additional CGs were selected from the literature, and quantitative real-time polymerase chain reaction (qPCR) was performed to analyse the expression of all identified CGs. Altogether, >40 genes presenting differential gene expression during drought acclimation were identified, some of them showing different expression profiles between drought-tolerant and susceptible clones. Based on the obtained results, it can be concluded that factors involved a complex network of responses probably involving the abscisic signalling pathway and nitric oxide are major molecular determinants that might explain the better efficiency in controlling stomata closure and transpiration displayed by drought-tolerant clones of C. canephora. 650 $aCafé 650 $aCoffea canephora 650 $aGenetics 653 $aCandidate gene 653 $aCoffea canephora 653 $aDifferential expression 653 $aDrought acclimation 653 $aGenética 653 $aProteomic 653 $aProteômica 653 $aReal time PCR 700 1 $aVINECKY, F. 700 1 $aALVES, G. S. C. 700 1 $aRAMOS, H. J. O. 700 1 $aELBELT, S. 700 1 $aVIEIRA, N. G. 700 1 $aCARNEIRO, F. A. 700 1 $aSUJII, P. S. 700 1 $aALEKCEVETCH, J. C. 700 1 $aSILVA, V. A. 700 1 $aDaMATTA, F. M. 700 1 $aFERRÃO, M. A. G. 700 1 $aLEROY, T. 700 1 $aPOT, D. 700 1 $aVIEIRA, L. G. E. 700 1 $aSILVA, F. R. da 700 1 $aANDRADE, A. C. 773 $tJournal of Experimental Botany, Oxford$gv. 63, n. 11, p. 4191-4212, 2012.
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