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Registro Completo |
Biblioteca(s): |
Embrapa Amazônia Oriental. |
Data corrente: |
20/11/2023 |
Data da última atualização: |
20/11/2023 |
Tipo da produção científica: |
Resumo em Anais de Congresso |
Autoria: |
ROSÁRIO, R. G. A. do; OLIVEIRA, M. do S. P. de; BENCHIMOL, R. L. |
Afiliação: |
RAQUEL GISELLI ASSIS DO ROSÁRIO; MARIA DO SOCORRO P DE OLIVEIRA, CPATU; RUTH LINDA BENCHIMOL, CPATU. |
Título: |
Laboratório de Fitopatologia da Embrapa Amazônia Oriental: diagnóstico de doenças fúngicas em açaizeiro no ano de 2022. |
Ano de publicação: |
2023 |
Fonte/Imprenta: |
In: SEMINÁRIO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA AMAZÔNIA ORIENTAL, 25., 2022, Belém, PA. Anais... Belém, PA: Embrapa Amazônia Oriental, 2023. |
Páginas: |
p. 48-49. |
Série: |
(Embrapa Amazônia Oriental. Eventos técnicos & científicos, 1). |
Idioma: |
Português |
Palavras-Chave: |
Bipolaris bicolor; Lasiodiplodia theobramae. |
Thesagro: |
Açaí; Colletotrichum Gloeosporioides; Doença de Planta; Doença Fúngica; Euterpe Oleracea. |
Thesaurus Nal: |
Pestalotiopsis. |
Categoria do assunto: |
-- |
URL: |
https://ainfo.cnptia.embrapa.br/digital/bitstream/doc/1158584/1/Pibic2022-49-50.pdf
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Marc: |
LEADER 00950nam a2200241 a 4500 001 2158584 005 2023-11-20 008 2023 bl uuuu u00u1 u #d 100 1 $aROSÁRIO, R. G. A. do 245 $aLaboratório de Fitopatologia da Embrapa Amazônia Oriental$bdiagnóstico de doenças fúngicas em açaizeiro no ano de 2022.$h[electronic resource] 260 $aIn: SEMINÁRIO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA AMAZÔNIA ORIENTAL, 25., 2022, Belém, PA. Anais... Belém, PA: Embrapa Amazônia Oriental$c2023 300 $ap. 48-49. 490 $a(Embrapa Amazônia Oriental. Eventos técnicos & científicos, 1). 650 $aPestalotiopsis 650 $aAçaí 650 $aColletotrichum Gloeosporioides 650 $aDoença de Planta 650 $aDoença Fúngica 650 $aEuterpe Oleracea 653 $aBipolaris bicolor 653 $aLasiodiplodia theobramae 700 1 $aOLIVEIRA, M. do S. P. de 700 1 $aBENCHIMOL, R. L.
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Embrapa Amazônia Oriental (CPATU) |
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| Acesso ao texto completo restrito à biblioteca da Embrapa Mandioca e Fruticultura. Para informações adicionais entre em contato com cnpmf.biblioteca@embrapa.br. |
Registro Completo
Biblioteca(s): |
Embrapa Mandioca e Fruticultura. |
Data corrente: |
25/09/2018 |
Data da última atualização: |
25/09/2018 |
Tipo da produção científica: |
Artigo em Periódico Indexado |
Circulação/Nível: |
A - 2 |
Autoria: |
SEREJO, J. A. dos S.; GARDINGO, J. R.; MONDIN, M.; AGUIAR-PERECIN, M. L. R. |
Afiliação: |
JANAY ALMEIDA DOS SANTOS SEREJO, CNPMF; JOSÉ R. GARDINGO, ESALQ; MATEUS MONDIN, ESALQ; MARGARIDA L. R. AGUIAR-PERECIN, ESALQ. |
Título: |
Alterations in heterochromatic knobs in maize callus culture by breakage-fusion-bridge cycle and unequal crossing over. |
Ano de publicação: |
2018 |
Fonte/Imprenta: |
Cytogenetic and Genome Research, v.154, p.107-118,2018. |
ISSN: |
1424-859X |
Idioma: |
Inglês |
Conteúdo: |
The meiotic and mitotic behavior of regenerated plants derived from a long-term callus culture, designated 12-F, was analyzed. This culture was heterozygous for an amplification of the heterochromatic knob on the long arm of chromosome 7 (K7L). We aimed to investigate if the amplification resulted from a breakage-fusion-bridge (BFB) cycle or from unequal sister chromatid recombination. Therefore, C-banded mitotic metaphases and pachytene, diakinesis, and anaphase I of regenerated plants were analyzed. Additionally, the occurrence of alterations in K7L was investigated in C-banded metaphases from short-term callus cultures derived from lines related to the donor genotype of the 12-F culture. As a result, plants homozygous and heterozygous for the amplification were detected. Meiosis was normal with few abnormalities, such as a low frequency of univalents at diakinesis. In the callus cultures a chromosome 7 with knobs of different sizes in the sister chromatids was detected and interpreted as a result of unequal crossing over. Other chromosomal alterations were consistent with the occurrence of BFB cycles. The finding of unequal crossing over in the cultures supports the conclusion that the amplification in the culture 12-F would be derived from this mechanism. If the amplification was derived from a BFB cycle, the terminal euchromatic segment between knob and the telomere would be deleted, and possibly, homozygous plants would not be viable. |
Thesagro: |
Milho. |
Thesaurus NAL: |
Callus culture. |
Categoria do assunto: |
-- |
Marc: |
LEADER 02071naa a2200193 a 4500 001 2096257 005 2018-09-25 008 2018 bl uuuu u00u1 u #d 022 $a1424-859X 100 1 $aSEREJO, J. A. dos S. 245 $aAlterations in heterochromatic knobs in maize callus culture by breakage-fusion-bridge cycle and unequal crossing over.$h[electronic resource] 260 $c2018 520 $aThe meiotic and mitotic behavior of regenerated plants derived from a long-term callus culture, designated 12-F, was analyzed. This culture was heterozygous for an amplification of the heterochromatic knob on the long arm of chromosome 7 (K7L). We aimed to investigate if the amplification resulted from a breakage-fusion-bridge (BFB) cycle or from unequal sister chromatid recombination. Therefore, C-banded mitotic metaphases and pachytene, diakinesis, and anaphase I of regenerated plants were analyzed. Additionally, the occurrence of alterations in K7L was investigated in C-banded metaphases from short-term callus cultures derived from lines related to the donor genotype of the 12-F culture. As a result, plants homozygous and heterozygous for the amplification were detected. Meiosis was normal with few abnormalities, such as a low frequency of univalents at diakinesis. In the callus cultures a chromosome 7 with knobs of different sizes in the sister chromatids was detected and interpreted as a result of unequal crossing over. Other chromosomal alterations were consistent with the occurrence of BFB cycles. The finding of unequal crossing over in the cultures supports the conclusion that the amplification in the culture 12-F would be derived from this mechanism. If the amplification was derived from a BFB cycle, the terminal euchromatic segment between knob and the telomere would be deleted, and possibly, homozygous plants would not be viable. 650 $aCallus culture 650 $aMilho 700 1 $aGARDINGO, J. R. 700 1 $aMONDIN, M. 700 1 $aAGUIAR-PERECIN, M. L. R. 773 $tCytogenetic and Genome Research$gv.154, p.107-118,2018.
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