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Registro Completo |
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Biblioteca(s): |
Embrapa Soja. |
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Data corrente: |
11/09/2003 |
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Data da última atualização: |
28/04/2006 |
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Autoria: |
EL-HUSNY, J. C.; ANDRADE, E. B. de; ALMEIDA, L. A. de; AGUILA, R. M.; KLEPKER, D.; MEYER, M. C.; SILVEIRA FILHO, A. |
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Título: |
Indicação de cultivares de soja para microrregião de Paragominas - PA. |
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Ano de publicação: |
2003 |
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Fonte/Imprenta: |
In: REUNIÃO DE PESQUISA DE SOJA DA REGIÃO CENTRAL DO BRASIL, 25., 2003, Uberaba. Resumos... Londrina: Embrapa Soja: EPAMIG: Fundação Triângulo, 2003. |
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Páginas: |
p. 92. |
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Série: |
(Embrapa Soja. Documentos, 209). |
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Idioma: |
Português |
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Notas: |
Organizado por Odilon Ferreira Saraiva, Regina Maria Villas Boas de Campos Leite. |
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Conteúdo: |
A microrregião de Paragominas, Estado do Pará, face ao interesse de Produtores Rurais e do Governo do Estado pelo incentivo à produção de soja, vem crescendo sua área plantada, e se constituindo em polo produtor de grãos no estado. A Embrapa Amazônia Oriental e a Embrapa Soja em atenção a essa demanda vem conduzindo experimentos visando avaliar o comportamento de cultivares de soja na região. Os experimentos foram instalados no campo experimental da Embrapa Amazônia Oriental que fica a cerca de 12 Km da cidade de Paragominas, a qual está localizada a 02º 57' 24" latitude Sul e altitude é de 85 m. A umidade relativa e a precipitação média anual na região é de 81% e 1.801 mm, respectivamente. Em experimentos conduzidos no período de 1997 a 2002, destacaram-se as cultivares: BRS Sambaíba, BRS Tracajá, BRS Babaçu, BRS Seridó RCH, com rendimentos médios de 3.861, 3.768, 3.431 e 3.258 kg/ha, respectivamente. Propõe-se com estes resultados, manter a indicação dessas cultivares para cultivo na microrregião de Paragominas.
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Categoria do assunto: |
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Marc: |
LEADER 01874naa a2200229 a 4500
001 1465007
005 2006-04-28
008 2003 bl uuuu u00u1 u #d
100 1 $aEL-HUSNY, J. C.
245 $aIndicação de cultivares de soja para microrregião de Paragominas - PA.
260 $c2003
300 $ap. 92.
490 $a(Embrapa Soja. Documentos, 209).
500 $aOrganizado por Odilon Ferreira Saraiva, Regina Maria Villas Boas de Campos Leite.
520 $aA microrregião de Paragominas, Estado do Pará, face ao interesse de Produtores Rurais e do Governo do Estado pelo incentivo à produção de soja, vem crescendo sua área plantada, e se constituindo em polo produtor de grãos no estado. A Embrapa Amazônia Oriental e a Embrapa Soja em atenção a essa demanda vem conduzindo experimentos visando avaliar o comportamento de cultivares de soja na região. Os experimentos foram instalados no campo experimental da Embrapa Amazônia Oriental que fica a cerca de 12 Km da cidade de Paragominas, a qual está localizada a 02º 57' 24" latitude Sul e altitude é de 85 m. A umidade relativa e a precipitação média anual na região é de 81% e 1.801 mm, respectivamente. Em experimentos conduzidos no período de 1997 a 2002, destacaram-se as cultivares: BRS Sambaíba, BRS Tracajá, BRS Babaçu, BRS Seridó RCH, com rendimentos médios de 3.861, 3.768, 3.431 e 3.258 kg/ha, respectivamente. Propõe-se com estes resultados, manter a indicação dessas cultivares para cultivo na microrregião de Paragominas.
700 1 $aANDRADE, E. B. de
700 1 $aALMEIDA, L. A. de
700 1 $aAGUILA, R. M.
700 1 $aKLEPKER, D.
700 1 $aMEYER, M. C.
700 1 $aSILVEIRA FILHO, A.
773 $tIn: REUNIÃO DE PESQUISA DE SOJA DA REGIÃO CENTRAL DO BRASIL, 25., 2003, Uberaba. Resumos... Londrina: Embrapa Soja: EPAMIG: Fundação Triângulo, 2003.
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Registro original: |
Embrapa Soja (CNPSO) |
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Biblioteca(s): |
Embrapa Meio Ambiente. |
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Data corrente: |
02/02/2016 |
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Data da última atualização: |
02/02/2016 |
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Tipo da produção científica: |
Artigo em Anais de Congresso |
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Autoria: |
DURÁN, N.; MARTINEZ, D. S. T.; JUSTO, G. Z.; LIMA, R. de; CASTRO, V. L. S. S. de; UMBUZEIRO, G. de A.; BARBIERI, E.; DURÁN, M.; MELO, P. da S.; ALVES, O. L.; FÁVARO, W. J. |
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Afiliação: |
NELSON DURAN, IQ-UNICAMP; DIEGO STEFANI TEODORO MARTINEZ, LNNANO-CNPEM; GISELLE ZENKER JUSTO, UNIFESP; RENATA DE LIMA, UNISO; VERA LUCIA SCHERHOLZ S DE CASTRO, CNPMA; GISELA DE ARAGAO UMBUZEIRO, Faculdade de Tecnologia - UNICAMP; EDSON BARBIERI, Instituto de Pesca - SP; MARCELA DURAN, IQ-UNICAMP; PATRICIA DA SILVA MELO, METROCAMP; OSVALDO LUIZ ALVES, IQ-UNICAMP; WAGNER JOSE FAVARO, IQ-UNICAMP. |
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Título: |
Interlab study on nanotoxicology of representative graphene oxide. |
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Ano de publicação: |
2015 |
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Fonte/Imprenta: |
Journal of Physics, Bristol, v. 617, p. 1-9, 2015. Edition of the proceedings 4th International Conference on Safe Production and Use Nanomaterials (Nanosafe 2014) 18-20 November 2014, held a Grenoble, France. |
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Idioma: |
Inglês |
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Conteúdo: |
Abstract: The graphene sample GO:Single-layer graphene oxide, purity 99%, thickness 0.7-1.2 nm (AFM); ~300-800nm X&Y dimensions is the standard size <450 nm & 1-20 ?m lateral dimensions. Cheap Tubes Inc., Bratleboro, USA was selected for our study. Exhaustive characterization of GO was afforded. It exhibited thermal stability over 60oC and it was suspended in deionized water after ultrasonication (1 mg/mL) (stable 10 days). All the biological fluids used in the different assays were used as control of the colloidal suspension stability. Then, all the studies were carried out within that stability period. The cytotoxicity assays were carried out by the Alamar Blue (Resazurin) reduction, MTT and flow cytometry assays in mouse embryonic fibroblast cells (3T3), human keratinocytes (HaCaT), colorectal cancer cells (Caco-2/HCT 116), Lewis lung cancer cells (3LL), acute myeloid leukemia cells (KG-1, Jurkat, Kasumi-1) and chronic myeloid leukemia cells (K562, Lucena) and no significant toxicity was found after exposition to 0.1-100 ug/mL for 24 and 48 h. Breast cancer cells, MCF-7, showed a 20% reduction on cell viability at 24 and 48 h. No cytotoxicity were found in lymphocytes, Chinese hamster ovary cells (CHO) and human macrophage cell line (U937) at 0.1-50 ug/mL, but 30-50% survival inhibition was observed at 100 ug/mL. A dose-dependent increase in apoptosis was observed in some cells (Kasumi-1, Jurkat and K562 cells). In the case of CHO and 3T3 cells, greater levels of necrosis with increasing concentrations of GO (>50 ug/mL) were observed. Genotoxic study using the Comet assay showed slight DNA damage in lymphocytes at all concentrations tested, while more significant effects was observed in CHO cells. Econanotoxicity was carried out by lethality assays in the nematode Caenorhabditis elegans,d in the freshwater coelenterate Hydra, Daphania amd in Shrimp with no signs of toxicity at concentrations varying from 0.1-100 ug/mL of GO. However, death and disintegration of Hydra was observed after exposition to 100 ug/mL for 72 h. In in vivo studies, no changes in biochemical parameters of Fischer 344 rats were observed after the i.p. administration of GO. Some black agglomerates were found in the intraperitoneal cavity of rats injected with GO. However, in Fisher 344 rats-bearing prostate tumors, treatment with GO (up to 100 ug/mL) negatively affected the hepatic parameters, whilst in the renal ones, an improvement was observed. Studies are in progress to understand the mechanisms involved in the uptake of GO by RES. GO appears as a potential non-toxic in vitro and in vivo assays at the concentrations used in this interlab experiments. MenosAbstract: The graphene sample GO:Single-layer graphene oxide, purity 99%, thickness 0.7-1.2 nm (AFM); ~300-800nm X&Y dimensions is the standard size <450 nm & 1-20 ?m lateral dimensions. Cheap Tubes Inc., Bratleboro, USA was selected for our study. Exhaustive characterization of GO was afforded. It exhibited thermal stability over 60oC and it was suspended in deionized water after ultrasonication (1 mg/mL) (stable 10 days). All the biological fluids used in the different assays were used as control of the colloidal suspension stability. Then, all the studies were carried out within that stability period. The cytotoxicity assays were carried out by the Alamar Blue (Resazurin) reduction, MTT and flow cytometry assays in mouse embryonic fibroblast cells (3T3), human keratinocytes (HaCaT), colorectal cancer cells (Caco-2/HCT 116), Lewis lung cancer cells (3LL), acute myeloid leukemia cells (KG-1, Jurkat, Kasumi-1) and chronic myeloid leukemia cells (K562, Lucena) and no significant toxicity was found after exposition to 0.1-100 ug/mL for 24 and 48 h. Breast cancer cells, MCF-7, showed a 20% reduction on cell viability at 24 and 48 h. No cytotoxicity were found in lymphocytes, Chinese hamster ovary cells (CHO) and human macrophage cell line (U937) at 0.1-50 ug/mL, but 30-50% survival inhibition was observed at 100 ug/mL. A dose-dependent increase in apoptosis was observed in some cells (Kasumi-1, Jurkat and K562 cells). In the case of CHO and 3T3 cells, greater levels of necrosis... Mostrar Tudo |
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Palavras-Chave: |
Fraphene oxide; Grafeno; Nanotecnologia. |
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Thesagro: |
Toxidez. |
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Thesaurus NAL: |
Nanomaterials; Nanoparticles; Toxicity. |
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Categoria do assunto: |
S Ciências Biológicas |
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URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/138246/1/2015AA038.pdf
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Marc: |
LEADER 03692nam a2200313 a 4500
001 2035854
005 2016-02-02
008 2015 bl uuuu u00u1 u #d
100 1 $aDURÁN, N.
245 $aInterlab study on nanotoxicology of representative graphene oxide.$h[electronic resource]
260 $aJournal of Physics, Bristol, v. 617, p. 1-9, 2015. Edition of the proceedings 4th International Conference on Safe Production and Use Nanomaterials (Nanosafe 2014) 18-20 November 2014, held a Grenoble, France.$c2015
520 $aAbstract: The graphene sample GO:Single-layer graphene oxide, purity 99%, thickness 0.7-1.2 nm (AFM); ~300-800nm X&Y dimensions is the standard size <450 nm & 1-20 ?m lateral dimensions. Cheap Tubes Inc., Bratleboro, USA was selected for our study. Exhaustive characterization of GO was afforded. It exhibited thermal stability over 60oC and it was suspended in deionized water after ultrasonication (1 mg/mL) (stable 10 days). All the biological fluids used in the different assays were used as control of the colloidal suspension stability. Then, all the studies were carried out within that stability period. The cytotoxicity assays were carried out by the Alamar Blue (Resazurin) reduction, MTT and flow cytometry assays in mouse embryonic fibroblast cells (3T3), human keratinocytes (HaCaT), colorectal cancer cells (Caco-2/HCT 116), Lewis lung cancer cells (3LL), acute myeloid leukemia cells (KG-1, Jurkat, Kasumi-1) and chronic myeloid leukemia cells (K562, Lucena) and no significant toxicity was found after exposition to 0.1-100 ug/mL for 24 and 48 h. Breast cancer cells, MCF-7, showed a 20% reduction on cell viability at 24 and 48 h. No cytotoxicity were found in lymphocytes, Chinese hamster ovary cells (CHO) and human macrophage cell line (U937) at 0.1-50 ug/mL, but 30-50% survival inhibition was observed at 100 ug/mL. A dose-dependent increase in apoptosis was observed in some cells (Kasumi-1, Jurkat and K562 cells). In the case of CHO and 3T3 cells, greater levels of necrosis with increasing concentrations of GO (>50 ug/mL) were observed. Genotoxic study using the Comet assay showed slight DNA damage in lymphocytes at all concentrations tested, while more significant effects was observed in CHO cells. Econanotoxicity was carried out by lethality assays in the nematode Caenorhabditis elegans,d in the freshwater coelenterate Hydra, Daphania amd in Shrimp with no signs of toxicity at concentrations varying from 0.1-100 ug/mL of GO. However, death and disintegration of Hydra was observed after exposition to 100 ug/mL for 72 h. In in vivo studies, no changes in biochemical parameters of Fischer 344 rats were observed after the i.p. administration of GO. Some black agglomerates were found in the intraperitoneal cavity of rats injected with GO. However, in Fisher 344 rats-bearing prostate tumors, treatment with GO (up to 100 ug/mL) negatively affected the hepatic parameters, whilst in the renal ones, an improvement was observed. Studies are in progress to understand the mechanisms involved in the uptake of GO by RES. GO appears as a potential non-toxic in vitro and in vivo assays at the concentrations used in this interlab experiments.
650 $aNanomaterials
650 $aNanoparticles
650 $aToxicity
650 $aToxidez
653 $aFraphene oxide
653 $aGrafeno
653 $aNanotecnologia
700 1 $aMARTINEZ, D. S. T.
700 1 $aJUSTO, G. Z.
700 1 $aLIMA, R. de
700 1 $aCASTRO, V. L. S. S. de
700 1 $aUMBUZEIRO, G. de A.
700 1 $aBARBIERI, E.
700 1 $aDURÁN, M.
700 1 $aMELO, P. da S.
700 1 $aALVES, O. L.
700 1 $aFÁVARO, W. J.
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