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 | Acesso ao texto completo restrito à biblioteca da Embrapa Soja. Para informações adicionais entre em contato com valeria.cardoso@embrapa.br. |
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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
18/12/2020 |
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Data da última atualização: |
18/12/2020 |
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Tipo da produção científica: |
Artigo em Periódico Indexado |
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Autoria: |
BRAGA, P.; CRUSIOL, L. G. T.; NANNI, M. R.; CARANHATO, A. L. H.; FUHRMANN, M. B.; NEPOMUCENO, A. L.; NEUMAIER, N.; FARIAS, J. R. B.; KOLTUN, A.; GONÇALVES, L. S. A.; MERTZ-HENNING, L. M. |
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Afiliação: |
P. Braga, Universidade Estadual de Londrina, UEL, Londrina, PR.; L. G. T. Crusiol, Universidade Estadual de Maringá (UEM), Maringá, PR.; M. R. Nanni, Universidade Estadual de Maringá (UEM), Maringá,PR.; A. L. H. Caranhato, Universidade Estadual de Londrina, UEL, Londrina, PR.; M. B. Fuhrmann, Universidade Estadual de Londrina, UEL, Londrina, PR.; ALEXANDRE LIMA NEPOMUCENO, CNPSO; NORMAN NEUMAIER, CNPSO; JOSE RENATO BOUCAS FARIAS, CNPSO; A. Koltun, niversidade Estadual de Maringá (UEM), Maringá, PR.; L. S. A. Gonçalves, Universidade Estadual de Londrina, UEL, Londrina, PR.; LILIANE MARCIA MERTZ HENNING, CNPSO. |
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Título: |
Vegetation indices and NIR-SWIR spectral bandsas a phenotyping tool for water status determination in soybean |
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Ano de publicação: |
2020 |
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Fonte/Imprenta: |
Precison agriculture, v. 1, 2020. |
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Páginas: |
18 p. |
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DOI: |
10.1007/s11119-020-09740-4 |
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Idioma: |
Inglês |
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Palavras-Chave: |
Fenotipagem de alto rendimento; High-throughput phenotyping. |
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Thesagro: |
Deficiência Hídrica; Glycine Max; Rendimento; Seca; Sensoriamento Remoto; Soja. |
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Thesaurus Nal: |
Drought; Remote sensing. |
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Categoria do assunto: |
F Plantas e Produtos de Origem Vegetal |
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Marc: |
LEADER 01084naa a2200373 a 4500
001 2128428
005 2020-12-18
008 2020 bl uuuu u00u1 u #d
024 7 $a10.1007/s11119-020-09740-4$2DOI
100 1 $aBRAGA, P.
245 $aVegetation indices and NIR-SWIR spectral bandsas a phenotyping tool for water status determination in soybean$h[electronic resource]
260 $c2020
300 $a18 p.
650 $aDrought
650 $aRemote sensing
650 $aDeficiência Hídrica
650 $aGlycine Max
650 $aRendimento
650 $aSeca
650 $aSensoriamento Remoto
650 $aSoja
653 $aFenotipagem de alto rendimento
653 $aHigh-throughput phenotyping
700 1 $aCRUSIOL, L. G. T.
700 1 $aNANNI, M. R.
700 1 $aCARANHATO, A. L. H.
700 1 $aFUHRMANN, M. B.
700 1 $aNEPOMUCENO, A. L.
700 1 $aNEUMAIER, N.
700 1 $aFARIAS, J. R. B.
700 1 $aKOLTUN, A.
700 1 $aGONÇALVES, L. S. A.
700 1 $aMERTZ-HENNING, L. M.
773 $tPrecison agriculture$gv. 1, 2020.
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Registro original: |
Embrapa Soja (CNPSO) |
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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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