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| Registros recuperados : 91 | |
| 8. |  | ANDRADE JÚNIOR, S. de; VENANCIO, F. C. D.; AMARAL, J. F. T. do; ESPINDULA, M. C.; VERDIN FILHO, A. C. Recipientes e substratos para produção de mudas de Coffea SP. In: FERREIRA, A.; LOPES, J. C.; FERREIRA, M. F. da S.; SOARES, T. C. B. (Org.). Tópicos Especiais em Produção Vegetal VI. Alegre, ES: CAUFES, 2016. p. 316 - 341.| Biblioteca(s): Embrapa Rondônia. |
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| 9. | | GONZALES, R. V.; ZAMBOLIM, L.; ALMEIDA, D. P.; CAIXETA, E. T.; ROSADO, R. D. S.; VERDIN-FILHO, A. C. Prospects for achieving multiple disease resistance with Coffea canephora clones. Australasian Plant Pathology, v. 52, n. 5, p. 451-462, 2023.| Biblioteca(s): Embrapa Café. |
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| 12. | | FERRAO, M. A. G.; FERRÃO, R. G.; FONSECA, A. F. A. da; SOUZA, E. M. R.; VERDIN FILHO, A. C.; VOLPI, P. S. Cruzamentos dialélicos em café conilon. In: SIMPÓSIO DE PESQUISA DOS CAFÉS DO BRASIL, 6., 2009, Vitória. Inovação científica, competitividade e mudanças climáticas: anais... Vitória: Consórcio Pesquisa Café, 2009.| Biblioteca(s): Embrapa Café. |
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| 13. | | FERRÃO, R. G.; FERRAO, M. A. G.; VOLPI, P. S.; FONSECA, A. F. A. da; VERDIN FILHO, A. C.; COMÉRIO, M. Cultivares de café conilon e robusta. Informe Agropecuário, v. 41, n. 309, p. 17-25, 2020.| Biblioteca(s): Embrapa Café. |
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| 14. | | FONSECA, A. F. A. da; FERRÃO, R. G.; FERRAO, M. A. G.; VOLPI, P. S.; VERDIN FILHO, A. C.; FAZUOLI, L. C. Cultivares de café robusta. In: CARVALHO, C. H. S. de (Ed.). Cultivares de café: origem, características e recomendações. Brasília, DF: Embrapa Café, 2008. 334 p. il. p. 255-280| Biblioteca(s): Embrapa Café. |
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| 15. | | FERRÃO, R. G.; FERRAO, M. A. G.; VOLPI, P. S.; FONSECA, A. F. A. da; VERDIN FILHO, A. C.; COMÉRIO, M. Cultivares de cafés Conilon e Robusta. Informe Agropecuário, v.41, n.309, p.17-25, 2020.| Biblioteca(s): Embrapa Café. |
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| 16. | | FERRÃO, R. G.; FERRAO, M. A. G.; FONSECA, A. F. A. da; MISTRO, J. C.; VOLPI, P. S.; VERDIN FILHO, A. C.; LANI, J. A. Cultivares. In: FONSECA, A. F. A. da; SAKIYAMA, N. S.; BORÉM, A. (Ed.). Café conilon: do plantio à colheita. Viçosa: Ed. UFV, 2015. p. 29-49| Biblioteca(s): Embrapa Café. |
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| 17. | | FONSECA, A. F. A. da; FERRÃO, M. A. G.; FERRÃO, R. G.; VERDIN FILHO, A. C.; VOLPI, P. S.; ZUCATELI, F. 'Conilon Vitória - Incaper 8142' : improved Coffea canephora var. kouillou clone cultivar for the state of Espírito Santo. Crop Breeding and Applied Biotechnology, Viçosa, MG, v. 4, n. 4, p. 503-505, Dec. 2004. Cultivar release.| Biblioteca(s): Embrapa Arroz e Feijão. |
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| 18. | | FONSECA, A. F. A. da; FERRÃO, M. A. G.; FERRÃO, R. G.; VERDIN FILHO, A. C.; VOLPI, P. S.; ZUCATELI, F. Conilon Vitória "Incaper 8142": variedade clonal de café Conilon. Vitória: Incaper, 2007; Brasília, DF: Embrapa Café, 2004. 23 p. il. Color. (Incaper. Documentos, 127).| Biblioteca(s): Embrapa Semiárido; Embrapa Unidades Centrais. |
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| Registros recuperados : 91 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Café. Para informações adicionais entre em contato com biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Café. |
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Data corrente: |
28/11/2023 |
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Data da última atualização: |
07/12/2023 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
A - 4 |
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Autoria: |
GONZALES, R. V.; ZAMBOLIM, L.; ALMEIDA, D. P.; CAIXETA, E. T.; ROSADO, R. D. S.; VERDIN-FILHO, A. C. |
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Afiliação: |
RAFAEL V. GONZALES, UNIVERSIDADE FEDERAL DE VIÇOSA; LAÉRCIO ZAMBOLIM, UNIVERSIDADE FEDERAL DE VIÇOSA; DÊNIA P. ALMEIDA, UNIVERSIDADE FEDERAL DE VIÇOSA; EVELINE TEIXEIRA CAIXETA MOURA, CNPCa; RENATO D. S. ROSADO, UNIVERSIDADE FEDERAL DE VIÇOSA; ABRAÃO C. VERDIN-FILHO, INSTITUTO CAPIXABA DE PESQUISA, ASSISTÊNCIA TÉCNICA E EXTENSÃO RURAL. |
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Título: |
Prospects for achieving multiple disease resistance with Coffea canephora clones. |
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Ano de publicação: |
2023 |
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Fonte/Imprenta: |
Australasian Plant Pathology, v. 52, n. 5, p. 451-462, 2023. |
|
DOI: |
https://doi.org/10.1007/s13313-023-00933-9 |
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Idioma: |
Inglês |
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Conteúdo: |
In the present work, it was phenotyped 29 Coffea canephora clones for resistance to Hemileia vastatrix races II and XXXIII and investigated the presence of molecular markers associated with Coffee Leaf Rust (CLR) and Coffee Berry Disease (CBD) resistance loci in 67 clones. Phenotyping for resistance was performed by evaluating six components of quantitative resistance using the leaf disc technique. The averages of the components were submitted to the Scott-Knott test and to the multivariate analysis to obtain the generalized Mahalanobis distance, which was used to group the clones by the unweighted pair-group method using arithmetic averages. In screening resistance to CLR, molecular markers were evaluated associated with two resistance loci. Three sequence characterized amplified regions (SCAR) and a simple sequence repeats (SSR) markers associated with the locus of SH3 gene (Locus A); a SCAR and a cleaved amplified polymorphic site (CAPS) associated with a locus of resistance to races I, II and pathotype 001 of H. vastatrix (Locus B). For screening resistance to CBD, two SSRs were associated with the locus of the resistance Ck-1 gene (Locus C) were evaluated. The phenotyped clones were grouped into five resistance classes for each H. vastatrix race. Fifteen clones have locus of resistance to races I, II, and the pathotype 001 of H. vastatrix. Three clones have the Ck-1 gene. These results support growers to choose resistant clones for crop composition and indicate potential sources of CLR and CBD resistance for C. canephora breeding programs. MenosIn the present work, it was phenotyped 29 Coffea canephora clones for resistance to Hemileia vastatrix races II and XXXIII and investigated the presence of molecular markers associated with Coffee Leaf Rust (CLR) and Coffee Berry Disease (CBD) resistance loci in 67 clones. Phenotyping for resistance was performed by evaluating six components of quantitative resistance using the leaf disc technique. The averages of the components were submitted to the Scott-Knott test and to the multivariate analysis to obtain the generalized Mahalanobis distance, which was used to group the clones by the unweighted pair-group method using arithmetic averages. In screening resistance to CLR, molecular markers were evaluated associated with two resistance loci. Three sequence characterized amplified regions (SCAR) and a simple sequence repeats (SSR) markers associated with the locus of SH3 gene (Locus A); a SCAR and a cleaved amplified polymorphic site (CAPS) associated with a locus of resistance to races I, II and pathotype 001 of H. vastatrix (Locus B). For screening resistance to CBD, two SSRs were associated with the locus of the resistance Ck-1 gene (Locus C) were evaluated. The phenotyped clones were grouped into five resistance classes for each H. vastatrix race. Fifteen clones have locus of resistance to races I, II, and the pathotype 001 of H. vastatrix. Three clones have the Ck-1 gene. These results support growers to choose resistant clones for crop composition and indicate potentia... Mostrar Tudo |
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Thesaurus NAL: |
Coffea canephora var. laurentii; Coffee berry disease; Genetic markers; Genetic resistance; Leaf rust; Phenotype. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02388naa a2200265 a 4500
001 2158783
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008 2023 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.1007/s13313-023-00933-9$2DOI
100 1 $aGONZALES, R. V.
245 $aProspects for achieving multiple disease resistance with Coffea canephora clones.$h[electronic resource]
260 $c2023
520 $aIn the present work, it was phenotyped 29 Coffea canephora clones for resistance to Hemileia vastatrix races II and XXXIII and investigated the presence of molecular markers associated with Coffee Leaf Rust (CLR) and Coffee Berry Disease (CBD) resistance loci in 67 clones. Phenotyping for resistance was performed by evaluating six components of quantitative resistance using the leaf disc technique. The averages of the components were submitted to the Scott-Knott test and to the multivariate analysis to obtain the generalized Mahalanobis distance, which was used to group the clones by the unweighted pair-group method using arithmetic averages. In screening resistance to CLR, molecular markers were evaluated associated with two resistance loci. Three sequence characterized amplified regions (SCAR) and a simple sequence repeats (SSR) markers associated with the locus of SH3 gene (Locus A); a SCAR and a cleaved amplified polymorphic site (CAPS) associated with a locus of resistance to races I, II and pathotype 001 of H. vastatrix (Locus B). For screening resistance to CBD, two SSRs were associated with the locus of the resistance Ck-1 gene (Locus C) were evaluated. The phenotyped clones were grouped into five resistance classes for each H. vastatrix race. Fifteen clones have locus of resistance to races I, II, and the pathotype 001 of H. vastatrix. Three clones have the Ck-1 gene. These results support growers to choose resistant clones for crop composition and indicate potential sources of CLR and CBD resistance for C. canephora breeding programs.
650 $aCoffea canephora var. laurentii
650 $aCoffee berry disease
650 $aGenetic markers
650 $aGenetic resistance
650 $aLeaf rust
650 $aPhenotype
700 1 $aZAMBOLIM, L.
700 1 $aALMEIDA, D. P.
700 1 $aCAIXETA, E. T.
700 1 $aROSADO, R. D. S.
700 1 $aVERDIN-FILHO, A. C.
773 $tAustralasian Plant Pathology$gv. 52, n. 5, p. 451-462, 2023.
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