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Registro Completo |
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Biblioteca(s): |
Embrapa Hortaliças. |
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Data corrente: |
03/06/2019 |
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Data da última atualização: |
03/06/2019 |
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Tipo da produção científica: |
Resumo em Anais de Congresso |
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Autoria: |
MACEDO, A. G.; PINHEIRO, J. B.; BISCAIA, D.; SOUZA, R. L.; BARBOSA, A. V. S.; SILVA, M. G.; MELLO, A. F. S.; SILVA, G. O. da. |
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Afiliação: |
A. G. MACEDO, UNIVERSIDADE DE BRASÍLIA; JADIR BORGES PINHEIRO, CNPH; DANIELLE BISCAIA, CNPH; R. L. SOUZA, ICESP; A. V. S. BARBOSA, ICESP; M. G. SILVA, UNIVERSIDADE DE BRASÍLIA; ALEXANDRE FURTADO SILVEIRA MELLO, CNPH; GIOVANI OLEGARIO DA SILVA, CNPH. |
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Título: |
Reação de cultivares comerciais e clones experimentais de Ipomoea batatas L. em campo naturalmente infestado com Meloidogyne javanica e M. incognita raça 1. |
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Ano de publicação: |
2019 |
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Fonte/Imprenta: |
In: CONGRESSO BRASILEIRO DE NEMATOLOGIA, 36, 2019, Caldas Novas. Nematoides: da Ciência ao Campo. [Anais, palestras e resumos]. Campinas: Infobibos, 2019. |
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Idioma: |
Português |
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Notas: |
Resumo. |
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Conteúdo: |
O objetivo deste trabalho foi avaliar a reação de cultivares e clones experimentais de batata-doce ao nematoide-das-galhas, a fim de incrementar a variabilidade de materiais disponíveis no mercado com resistência a este patógeno de solo. |
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Thesagro: |
Batata Doce; Meloidogyne spp; Nematóide. |
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Categoria do assunto: |
-- |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/198043/1/Resumo36CBN-0021.pdf
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Marc: |
LEADER 01108nam a2200241 a 4500
001 2109570
005 2019-06-03
008 2019 bl uuuu u00u1 u #d
100 1 $aMACEDO, A. G.
245 $aReação de cultivares comerciais e clones experimentais de Ipomoea batatas L. em campo naturalmente infestado com Meloidogyne javanica e M. incognita raça 1.$h[electronic resource]
260 $aIn: CONGRESSO BRASILEIRO DE NEMATOLOGIA, 36, 2019, Caldas Novas. Nematoides: da Ciência ao Campo. [Anais, palestras e resumos]. Campinas: Infobibos$c2019
500 $aResumo.
520 $aO objetivo deste trabalho foi avaliar a reação de cultivares e clones experimentais de batata-doce ao nematoide-das-galhas, a fim de incrementar a variabilidade de materiais disponíveis no mercado com resistência a este patógeno de solo.
650 $aBatata Doce
650 $aMeloidogyne spp
650 $aNematóide
700 1 $aPINHEIRO, J. B.
700 1 $aBISCAIA, D.
700 1 $aSOUZA, R. L.
700 1 $aBARBOSA, A. V. S.
700 1 $aSILVA, M. G.
700 1 $aMELLO, A. F. S.
700 1 $aSILVA, G. O. da
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Registro original: |
Embrapa Hortaliças (CNPH) |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Florestas. Para informações adicionais entre em contato com cnpf.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Florestas. |
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Data corrente: |
04/01/2022 |
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Data da última atualização: |
04/03/2022 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Circulação/Nível: |
B - 1 |
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Autoria: |
TORRES-DINI, D.; DELGADO-CERRONE, L.; LUNA, L.; RESQUIN, F.; AGUIAR, A. V. de; SEBBENN, A. M. |
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Afiliação: |
DIEGO TORRES-DINI, INIA; LEONARDO DELGADO-CERRONE, Clemente Estable Biological Research Institute; LORENA LUNA, Centro Universitario de Tacuarembó; FERNANDO RESQUIN, INIA; ANANDA VIRGINIA DE AGUIAR, CNPF; ALEXANDRE MAGNO SEBBENN, Instituto Florestal. |
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Título: |
The traceability of Eucalyptus clones using molecular markers. |
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Ano de publicação: |
2021 |
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Fonte/Imprenta: |
Silvae Genetica, v. 70, p. 217-225, 2021. |
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DOI: |
https://doi.org/10.2478/sg-2021-0019 |
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Idioma: |
Inglês |
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Conteúdo: |
The improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (PI) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( o H ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is structured in four clusters, while the E. globulus population consists of two clusters. MenosThe improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (PI) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( o H ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is structured in f... Mostrar Tudo |
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Palavras-Chave: |
Clone certification; Identity; Multiplex; Nurseries. |
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Thesagro: |
Eucalipto. |
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Thesaurus NAL: |
Clones; Eucalyptus; Genotyping; Traceability. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 02383naa a2200301 a 4500
001 2138721
005 2022-03-04
008 2021 bl uuuu u00u1 u #d
024 7 $ahttps://doi.org/10.2478/sg-2021-0019$2DOI
100 1 $aTORRES-DINI, D.
245 $aThe traceability of Eucalyptus clones using molecular markers.$h[electronic resource]
260 $c2021
520 $aThe improvement of Eucalyptus clones plays a crucial role in modern silviculture. This study used a set of 17 microsatellite loci to analyze the genetic diversity and structure of 107 elite clones (80 E. grandis and 27 E. globulus). All clones were cultivated in Uruguay and were sourced from three different providers. Using the fingerprinting technique, an exclusive molecular profile was assigned for each clone, and the genotyping reaction showed differences between the two species. The cumulative probability of identifying two random individuals that share the same genotype (PI) with all 17 loci, was estimated as low for E. grandis (1.18×10-15) and E. globulus (4.03×10-14). The combined PIsibs was (1.05×10-5) and (2.17×10-5) for E. grandis and E. globulus, respectively. A total of 180 alleles were detected for E. grandis and 100 for E. globulus. We found a high mean number of alleles per locus (10 for E. grandis and 6 for E. globulus), and the results for mean polymorphic information content ( PIC ) were (0.648) and (0.548), respectively. The observed heterozygosity ( o H ) ranged from 0.216 to 0.838 (mean = 0.509) for E. grandis and 0 to 1 (mean = 0.566) for E. globulus. Two core sets of seven EST-SSR loci were identified for each species. These markers revealed unambiguous fragment amplification, providing a minimum number of SSRs for effective clonal identification. The genetic structure analysis suggests that the germplasm of the E. grandis population is structured in four clusters, while the E. globulus population consists of two clusters.
650 $aClones
650 $aEucalyptus
650 $aGenotyping
650 $aTraceability
650 $aEucalipto
653 $aClone certification
653 $aIdentity
653 $aMultiplex
653 $aNurseries
700 1 $aDELGADO-CERRONE, L.
700 1 $aLUNA, L.
700 1 $aRESQUIN, F.
700 1 $aAGUIAR, A. V. de
700 1 $aSEBBENN, A. M.
773 $tSilvae Genetica$gv. 70, p. 217-225, 2021.
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