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| Registros recuperados : 13 | |
| 2. |  | HUNGRIA, M.; LOUREIRO, M. F.; MENDES, I. C.; CAMPO, R. J.; GRAHAM, P. H. Inoculant preparation, production and application. In: WERNER, D.; NEWTON, W. E. (ed.). Nitrogen fixation in agriculture, forestry, ecology, and the environment. Dordrecht: Springer, 2005. p. 223-253.| Biblioteca(s): Embrapa Agrobiologia; Embrapa Soja. |
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| 3. | | CRISPINO, C. C.; FRANCHINI, J. C.; ARIHARA, J.; LOUREIRO, M. F.; CAMPO, R. J.; HUNGRIA, M. Inoculation and N-fertilizer application in the soybean crop. In: CONGRESSO BRASILEIRO DE SOJA, 2.; MERCOSOJA 2002, 2002, Foz do Iguaçu. Perspectivas do agronegócio da soja: resumos. Londrina: Embrapa Soja, 2002. p. 206. (Embrapa Soja. Documentos, 181). Organizado por Odilon Ferreira Saraiva, Clara Beatriz Hoffmann-Campo.| Biblioteca(s): Embrapa Soja. |
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| 4. | | TRALDI, A. de S.; LOUREIRO, M. F. P.; CAPEZZUTO, A.; MAZORRA, A. L. Métodos de controle da atividade reprodutiva em caprinos. Revista Brasileira de Reprodução Animal, Belo Horizonte, v. 31, n. 2, p. 254-260, abr./jun., 2007. Palestra apresentada no XVII Congresso Brasileiro de Reprodução Animal, maio de 2007, Curitiba.| Biblioteca(s): Embrapa Caprinos e Ovinos. |
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| 10. | | SANTOS, A. B. dos; REIS JÚNIOR, F. B. dos; LOPES, A. C.; MENDES, I. C.; SIMON, M. F.; FARIA, S. M. de; LOUREIRO, M. F.; GROSS, E.; ELLIOTT, G. N.; BONTEMPS, C. Avaliação da capacidade simbiótica de estirpes de "beta-rizóbios" isoladas de nódulos de diferentes espécies de Mimosa. In: SIMPÓSIO NACIONAL CERRADO, 9.; SIMPÓSIO INTERNACIONAL SAVANAS TROPICAIS, 2., 2008, Brasília, DF. Desafios e estratégias para o equilíbrio entre sociedade, agronegócio e recursos naturais: anais... Planaltina, DF: Embrapa Cerrados, 2008. 1 CD-ROM.| Biblioteca(s): Embrapa Cerrados. |
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| 11. | | HUNGRIA, M.; CAMPO, R. J.; ANDRADE, D. S.; MENDES, I. C.; CHUEIRE, L. M. O.; GRANGE, L.; FERREIRA, M. C.; ALBERTON, O.; KASCHUK, G.; LOUREIRO, M. F.; PEDROSA, F. O. Genetic diversity of symbiotic rhizobia in brazilian soils. In: REUNIÃO ANUAL DA SOCIEDADE BRASILEIRA DE BIOQUÍMICA E BIOLOGIA MOLECULAR, 31., 2002, Caxambu. Programa e resumos. São Paulo : SBBq, 2002. p.29.| Biblioteca(s): Embrapa Soja. |
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| 12. | | JAMES, E. K.; ELLIOTT, G. N.; CHEN, W. -M.; BONTEMPS, C.; YOUNG, J. P. W.; FARIA, S. M. de; REIS JR. F. B. dos; SIMON, M. F.; GROSS, E.; LOUREIRO, M. F.; REIS, V. M.; PERIN, L.; BODDEY, R. M.; HUGHES, C. E.; MOULIN, L.; PRESCOTT, A. R.; SPRENT, J. I. Infection of legumes by beta-rhizobia In: DAKORA, F.D. et al. (ed.). INTERNATIONAL NITROGEN FIXATION CONGRESS, 15th., INTERNATIONAL CONFERENCE OF THE AFRICAN ASSOCIATION FOR BIOLOGICAL NITROGEN FIXATION, 12th., 2008, South Africa. Biological nitrogen fixation: towards poverty alleviation through sustainable agriculture: proceedings... Heidelberg: Springer, 2008. (Current Plant Science and Biotechnology in Agriculture, 42)| Biblioteca(s): Embrapa Agrobiologia; Embrapa Cerrados. |
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| 13. | | REIS JUNIOR, F. B. dos; SIMON, M. F.; GROSS, E.; BODDEY, R. M.; ELLIOT, G. N.; NETO, N. E.; LOUREIRO, M. F.; QUEIRÓZ, L. P.; CHEN, W. M.; NOREN, A.; FARIA, S. M. de; BONTEMPS, S. M.; BONTEMPS, C.; GOI, S. R.; YOUNG, J. P. W.; YOUNG, J. P. W.; SPRENT, J. I.; JAMES, E. K. Nodulation of mimosoid and other legumes by B-rhizobia: taxonomic and geographical aspects. In: CONGRESSO BRASILEIRO DE FISIOLOGIA VEGETAL, 12., 2009, Fortaleza. Resumos... Fortaleza: Sociedade Brasileira de Fisiologia Vegetal, 2009.| Biblioteca(s): Embrapa Agrobiologia. |
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| Registros recuperados : 13 | |
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 | Acesso ao texto completo restrito à biblioteca da Embrapa Agrobiologia. Para informações adicionais entre em contato com cnpab.biblioteca@embrapa.br. |
Registro Completo
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Biblioteca(s): |
Embrapa Agrobiologia. |
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Data corrente: |
25/01/1999 |
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Data da última atualização: |
25/01/1999 |
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Autoria: |
LOUREIRO, M. F.; JAMES, E. K.; SPRENT, J. I.; FRANCO, A. A. |
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Título: |
Stem and root nodules on the tropical wetland legume Aeschynomene flu minensis. |
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Ano de publicação: |
1995 |
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Fonte/Imprenta: |
New Phytologist, Oxford, v. 130, n. 4, p. 531-544, 1995. |
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Idioma: |
Inglês |
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Conteúdo: |
Aeschynomene fluminensis Vell., originally obtained from flooded areas of the Pantanal Matogrossense region of Brazil, was grown under stem-flooded or non-floodeed conditions for 70 d after inoculation with isolates of photosynthetic stem nodule rhizobia obtained from native A. fluminensis. Stem nodules formed only on submerged stems of flooded plants (mean of 25 per plant), and did not form on aerial parts, although they were capable of growing and fixing N2 after drainage of the stems. Root nodules formed on both non-flooded and flooded plants but were usually decreased in number by flooding (from means of 124 to 51 per plant, respectively). Flooding (and stem-nodulation) resulted in an increase in shoot (and a decrease in root) dry weight, regardless of rhizobial isolate. Stem nodules were attached by a wide collar of aerenchymatous tissue at the base of the nodule. There were large air spaces in the stem where nodules were subtended and these were continuous with nodule aerenchyma/outer cortex. In addition, aerenchyma and spongy tissue at the base of the nodule connected both flooded and non-flooded root nodules to large intercellular spaces in the root cortex. The stem and root nodules were ovoid in shape, and essentially aeschynomenoid in type, i.e. the central infected tissue was without uninfected, interstitial cells. Root nodules had a similar structure to stem nodules (although stem nodules were generally larger), and flooded root nodules were approximately twice the size of non-flooded nodules. The infected tissue of root and stem nodules consisted of spherical, bacteroid-containing cells containing one or two rod-shaped bacteroids per peribacteroid unit and prominent organelles. Infection threads were observed in root but not in stem nodules. The cortex of stem and root nodules had an apparent oxygen diffusion barrier, consisting of concentric layers of small cells with interlocking cell walls and few intercellular spaces. Cell layers external to these consisted of larger cells and intercellular spaces, with some spaces being occluded with an electron-dense material that contained a glycoprotein recognized by the monoclonal antibodies MAC236 and MAC265. The amount of glycoprotein occlusions did not appear to differ between nodule types or treatments, although stem nodules contained intracellular glycoprotein vesicles adjacent to cells walls. The exterior of the nodules consisted of an epidermis of thin flattened cells with occasional lenticels. Amyloplasts were common in lower stem and hypocotyl nodules, but fewer in flooded or non-flooded root nodules. Upper stem nodules (i.e. those within 6 cm of the water surface) differed from more profoundly submerged stem nodules by having chloroplasts throughout the cortex. Root nodules did not contain chloroplasts, and undifferentiated plastides were found mainly in lower stem nodules. MenosAeschynomene fluminensis Vell., originally obtained from flooded areas of the Pantanal Matogrossense region of Brazil, was grown under stem-flooded or non-floodeed conditions for 70 d after inoculation with isolates of photosynthetic stem nodule rhizobia obtained from native A. fluminensis. Stem nodules formed only on submerged stems of flooded plants (mean of 25 per plant), and did not form on aerial parts, although they were capable of growing and fixing N2 after drainage of the stems. Root nodules formed on both non-flooded and flooded plants but were usually decreased in number by flooding (from means of 124 to 51 per plant, respectively). Flooding (and stem-nodulation) resulted in an increase in shoot (and a decrease in root) dry weight, regardless of rhizobial isolate. Stem nodules were attached by a wide collar of aerenchymatous tissue at the base of the nodule. There were large air spaces in the stem where nodules were subtended and these were continuous with nodule aerenchyma/outer cortex. In addition, aerenchyma and spongy tissue at the base of the nodule connected both flooded and non-flooded root nodules to large intercellular spaces in the root cortex. The stem and root nodules were ovoid in shape, and essentially aeschynomenoid in type, i.e. the central infected tissue was without uninfected, interstitial cells. Root nodules had a similar structure to stem nodules (although stem nodules were generally larger), and flooded root nodules were approximately twice ... Mostrar Tudo |
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Palavras-Chave: |
Aeschynomene fluminensis; BNF; FBN; Fixação biologica de nitrogênio; Nitrogen fixing bacteria; O2. |
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Thesagro: |
Caule; Drenagem; Oxigênio; Solo Úmido. |
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Thesaurus NAL: |
drainage; oxygen; stems; wetlands. |
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Categoria do assunto: |
-- |
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Marc: |
LEADER 03729naa a2200325 a 4500
001 1620970
005 1999-01-25
008 1995 bl uuuu u00u1 u #d
100 1 $aLOUREIRO, M. F.
245 $aStem and root nodules on the tropical wetland legume Aeschynomene flu minensis.
260 $c1995
520 $aAeschynomene fluminensis Vell., originally obtained from flooded areas of the Pantanal Matogrossense region of Brazil, was grown under stem-flooded or non-floodeed conditions for 70 d after inoculation with isolates of photosynthetic stem nodule rhizobia obtained from native A. fluminensis. Stem nodules formed only on submerged stems of flooded plants (mean of 25 per plant), and did not form on aerial parts, although they were capable of growing and fixing N2 after drainage of the stems. Root nodules formed on both non-flooded and flooded plants but were usually decreased in number by flooding (from means of 124 to 51 per plant, respectively). Flooding (and stem-nodulation) resulted in an increase in shoot (and a decrease in root) dry weight, regardless of rhizobial isolate. Stem nodules were attached by a wide collar of aerenchymatous tissue at the base of the nodule. There were large air spaces in the stem where nodules were subtended and these were continuous with nodule aerenchyma/outer cortex. In addition, aerenchyma and spongy tissue at the base of the nodule connected both flooded and non-flooded root nodules to large intercellular spaces in the root cortex. The stem and root nodules were ovoid in shape, and essentially aeschynomenoid in type, i.e. the central infected tissue was without uninfected, interstitial cells. Root nodules had a similar structure to stem nodules (although stem nodules were generally larger), and flooded root nodules were approximately twice the size of non-flooded nodules. The infected tissue of root and stem nodules consisted of spherical, bacteroid-containing cells containing one or two rod-shaped bacteroids per peribacteroid unit and prominent organelles. Infection threads were observed in root but not in stem nodules. The cortex of stem and root nodules had an apparent oxygen diffusion barrier, consisting of concentric layers of small cells with interlocking cell walls and few intercellular spaces. Cell layers external to these consisted of larger cells and intercellular spaces, with some spaces being occluded with an electron-dense material that contained a glycoprotein recognized by the monoclonal antibodies MAC236 and MAC265. The amount of glycoprotein occlusions did not appear to differ between nodule types or treatments, although stem nodules contained intracellular glycoprotein vesicles adjacent to cells walls. The exterior of the nodules consisted of an epidermis of thin flattened cells with occasional lenticels. Amyloplasts were common in lower stem and hypocotyl nodules, but fewer in flooded or non-flooded root nodules. Upper stem nodules (i.e. those within 6 cm of the water surface) differed from more profoundly submerged stem nodules by having chloroplasts throughout the cortex. Root nodules did not contain chloroplasts, and undifferentiated plastides were found mainly in lower stem nodules.
650 $adrainage
650 $aoxygen
650 $astems
650 $awetlands
650 $aCaule
650 $aDrenagem
650 $aOxigênio
650 $aSolo Úmido
653 $aAeschynomene fluminensis
653 $aBNF
653 $aFBN
653 $aFixação biologica de nitrogênio
653 $aNitrogen fixing bacteria
653 $aO2
700 1 $aJAMES, E. K.
700 1 $aSPRENT, J. I.
700 1 $aFRANCO, A. A.
773 $tNew Phytologist, Oxford$gv. 130, n. 4, p. 531-544, 1995.
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