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Registro Completo |
Biblioteca(s): |
Embrapa Amapá. |
Data corrente: |
17/08/2007 |
Data da última atualização: |
14/10/2022 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Autoria: |
OLIVEIRA, L. P. S. de; SOUZA, G. D. de; SILVA, R. A. da. |
Afiliação: |
LANA PATRICIA SANTOS DE OLIVEIRA, UNIVERSIDADE FEDERAL DO AMAPÁ; GIZELLE DIAS DE SOUZA, UNIVERSIDADE FEDERAL DO AMAPÁ; RICARDO ADAIME DA SILVA, CPAF-AP. |
Título: |
Cerconota anonella (Sepp., 1830) (Lepidoptera: oecophoridae), a principal praga da gravioleira. |
Ano de publicação: |
2004 |
Fonte/Imprenta: |
Revista Científica Eletrônica de Agronomia, v. 3, n. 5, jun. 2004. |
Idioma: |
Português |
Conteúdo: |
O presente trabalho objetiva reunir informações sobre Cerconota anonella (Sepp., 1830) (Lepidoptera: Oecophoridae), a praga mais importante da gravioleira no Brasil. |
Thesagro: |
Annona Muricata; Dano; Praga. |
Categoria do assunto: |
O Insetos e Entomologia |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/178326/1/CPAF-AP-2004-Cerconota-anonella.pdf
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Marc: |
LEADER 00701naa a2200181 a 4500 001 1345272 005 2022-10-14 008 2004 bl uuuu u00u1 u #d 100 1 $aOLIVEIRA, L. P. S. de 245 $aCerconota anonella (Sepp., 1830) (Lepidoptera$boecophoridae), a principal praga da gravioleira. 260 $c2004 520 $aO presente trabalho objetiva reunir informações sobre Cerconota anonella (Sepp., 1830) (Lepidoptera: Oecophoridae), a praga mais importante da gravioleira no Brasil. 650 $aAnnona Muricata 650 $aDano 650 $aPraga 700 1 $aSOUZA, G. D. de 700 1 $aSILVA, R. A. da 773 $tRevista Científica Eletrônica de Agronomia$gv. 3, n. 5, jun. 2004.
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Embrapa Amapá (CPAF-AP) |
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Registro Completo
Biblioteca(s): |
Embrapa Unidades Centrais. |
Data corrente: |
16/10/1998 |
Data da última atualização: |
30/07/2019 |
Autoria: |
CONCEICAO, A. da S.; MATSUMOTO, K.; BAKRY, F.; BERND, R. B. |
Afiliação: |
ALEXANDRE DA SILVA CONCEIÇÃO, CENARGEN; KAZUMITSU MATSUMOTO, CENARGEN; FREDERIC BAKRY, CIRAD/FLHOR; REGINA BEATRIZ BERND, Cenargen. |
Título: |
Plant regeneration from long-term callus culture of aaa-group dessert banana. |
Ano de publicação: |
1998 |
Fonte/Imprenta: |
Pesquisa Agropecuária Brasileira, Brasília, DF, v. 33, n. 8, p. 1291-96, ago. 1998 |
Idioma: |
Inglês |
Notas: |
Título em português: Regeneração de plantas de bananeira do grupo AAA a partir de calos cultivados durante longo período. |
Conteúdo: |
The banana plant is one of the most widely cultivated crops in the world. However, banana breeding has been a slow process, due to the low seed set and low germination rates. Selection of useful somaclonal variations and genetic transformation in cells or calluses are promising techniques to accelerate the breeding process. Therefore, callus culture was carried out, aiming the establishment of one protocol for plant regeneration, to be used in banana breeding program. Leaf sheath disks of 'Nanicao' banana (Musa sp., AAA group, Cavendish subgroup) were cultured on a Murashige and Skoog (MS) basal medium supplemented with activated charcoal (0.2%), MES (2 [N-morpholino] ethanesulfonic acid) (15.3 mM) arginine (300 mM), Picloram (414 M) and 2iP (2-isopenteny adenine) (492 M). Globular calluses developed on the leaf tissue were subcultured in the same medium, acquiring a friable and translucid appearance after one and a half year of culture. The friable calluses were transferred to the medium without growth regulators and arginine, and supplemented with casein hydrolysate (0.05%), where they formed embryo-like structures after transference to light. From these structures, shoots with roots were obtained and plantlets developed. The plant regeneration protocol shown here may be useful to banana breeding via somaclonal variation. |
Palavras-Chave: |
Cultura de tecidos. |
Thesaurus NAL: |
Musa; tissue culture. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/item/45031/1/PLANT-REGENERATION-FROM.pdf
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Marc: |
LEADER 02051naa a2200205 a 4500 001 1095718 005 2019-07-30 008 1998 bl uuuu u00u1 u #d 100 1 $aCONCEICAO, A. da S. 245 $aPlant regeneration from long-term callus culture of aaa-group dessert banana. 260 $c1998 500 $aTítulo em português: Regeneração de plantas de bananeira do grupo AAA a partir de calos cultivados durante longo período. 520 $aThe banana plant is one of the most widely cultivated crops in the world. However, banana breeding has been a slow process, due to the low seed set and low germination rates. Selection of useful somaclonal variations and genetic transformation in cells or calluses are promising techniques to accelerate the breeding process. Therefore, callus culture was carried out, aiming the establishment of one protocol for plant regeneration, to be used in banana breeding program. Leaf sheath disks of 'Nanicao' banana (Musa sp., AAA group, Cavendish subgroup) were cultured on a Murashige and Skoog (MS) basal medium supplemented with activated charcoal (0.2%), MES (2 [N-morpholino] ethanesulfonic acid) (15.3 mM) arginine (300 mM), Picloram (414 M) and 2iP (2-isopenteny adenine) (492 M). Globular calluses developed on the leaf tissue were subcultured in the same medium, acquiring a friable and translucid appearance after one and a half year of culture. The friable calluses were transferred to the medium without growth regulators and arginine, and supplemented with casein hydrolysate (0.05%), where they formed embryo-like structures after transference to light. From these structures, shoots with roots were obtained and plantlets developed. The plant regeneration protocol shown here may be useful to banana breeding via somaclonal variation. 650 $aMusa 650 $atissue culture 653 $aCultura de tecidos 700 1 $aMATSUMOTO, K. 700 1 $aBAKRY, F. 700 1 $aBERND, R. B. 773 $tPesquisa Agropecuária Brasileira, Brasília, DF$gv. 33, n. 8, p. 1291-96, ago. 1998
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