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2. | | SANTOS, F. G. R. dos; OLIVEIRA, L. B. de; GONÇALVES, J. de L.; MACIEL, M. do V.; SILVA, J. K. da; CAVALCANTE, A. C. R. Famílias botânicas presentes em três sítios de pastejo. In: ENCONTRO DE INICIAÇÃO CIENTÍFICA DA EMBRAPA CAPRINOS E OVINOS, 4., 2015, Sobral. Anais... Sobral: Embrapa Caprinos e Ovinos, 2015. p. 24-25. Biblioteca(s): Embrapa Caprinos e Ovinos. |
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4. | | TEIXEIRA, C. de J. V.; PEREIRA, H. S.; MELO, L. C.; VIANELLO, R. P.; BORBA, T. C. de O. Análise de polimorfismo de locos microssátelites em feijoeiro comum. In: SEMINÁRIO JOVENS TALENTOS, 5., 2011, Santo Antônio de Goiás. Resumos apresentados. Santo Antônio de Goiás: Embrapa Arroz e Feijão, 2011. p. 15. (Embrapa Arroz e Feijão. Documentos, 270). Biblioteca(s): Embrapa Arroz e Feijão. |
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6. | | MOITAS, M. L.; FARINAS, C. S.; BERTUCCI NETO, V.; COURI, S. Caracterização do extrato de enzimas hidrolíticas produzido por fermentação semi-sólida. In: JORNADA DE INICIAÇÃO CIENTÍFICA E TECNOLÓGICA; CONGRESSO DE INICIAÇÃO CIENTÍFICA, 16.; CONGRESSO DE INICIAÇÃO EM DESENVOLVIMENTO TECNOLÓGICO E INOVAÇÃO, 1., 2008, São Carlos, SP. Anais de Eventos da UFSCar... São Carlos: UFSCar, 2008. v. 4 p. 176. Resumo. Biblioteca(s): Embrapa Instrumentação. |
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7. | | SILVA, J. J. da; DANIEL, O.; PADOVAN, M. P. Sistemas Agroflorestais para a Mesorregião Sudoeste de Mato Grosso do Sul: um estudo propositivo. In: SEMINÁRIO DE AGROECOLOGIA DE MATO GROSSO DO SUL, 2., 2008, Dourados. A construção participativa da agroecologia em Mato Grosso do Sul: anais. Dourados: Embrapa Agropecuária Oeste, 2008. 1 CD-ROM. Organizado por: Alberto Feiden, Milton Parron Padovan, Adalgiza Inês Campolim, Aurélio Vinícius Borsato, Ivo de Sá Motta, João Batista Catto, Tércio Jacques Fehlauer. Biblioteca(s): Embrapa Agropecuária Oeste. |
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13. | | NOGUEIRA, O. L.; CALZAVARA, B. B. G.; MULLER, C. H.; CARVALHO, C. J. R. de; GALVAO, E. U. P.; SILVA, H. M. e; RODRIGUES, J. E. L. F.; CARVALHO, J. E. U. de; OLIVEIRA, M. do S. P. de; ROCHA NETO, O. G. da; NASCIMENTO, W. M. O. do. A cultura da pupunha. Brasília, DF: EMBRAPA-SPI; Belém, PA: EMBRAPA-CPATU, 1995. 50 p. il. (Coleção plantar, 25). Biblioteca(s): Embrapa Acre; Embrapa Agroindústria de Alimentos; Embrapa Algodão; Embrapa Amazônia Ocidental; Embrapa Amazônia Oriental; Embrapa Meio Norte / UEP-Parnaíba; Embrapa Pantanal; Embrapa Recursos Genéticos e Biotecnologia; Embrapa Rondônia; Embrapa Roraima; Embrapa Solos; Embrapa Unidades Centrais; Embrapa Uva e Vinho. MenosEmbrapa Acre; Embrapa Agroindústria de Alimentos; Embrapa Algodão; Embrapa Amazônia Ocidental; Embrapa Amazônia Oriental; Embrapa Meio Norte / UEP-Parnaíba; Embrapa Pantanal; Embrapa Recursos Genéticos e Biotecnologia; Embrapa Rondônia; Embrapa Roraima... Mostrar Todas |
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14. | | GAYET, J. P.; BLEINROTH, E. W.; MATALLO, M.; GARCIA, E. E. C.; GARCIA, A. E.; ARDITO, E. F. G.; BORDIN, M. R. Abacate para exportação: procedimentos de colheita e pós-colheita. Brasília, DF: MAARA; EMBRAPA-SPI, 1995. 37 p. (Publicações técnicas FRUPEX, 15). Biblioteca(s): Embrapa Agroindústria Tropical; Embrapa Agropecuária Oeste; Embrapa Amapá; Embrapa Amazônia Oriental; Embrapa Clima Temperado; Embrapa Mandioca e Fruticultura; Embrapa Meio Ambiente; Embrapa Meio Norte / UEP-Parnaíba; Embrapa Meio-Norte; Embrapa Pantanal; Embrapa Rondônia; Embrapa Roraima; Embrapa Semiárido; Embrapa Solos; Embrapa Tabuleiros Costeiros; Embrapa Unidades Centrais; Embrapa Uva e Vinho. MenosEmbrapa Agroindústria Tropical; Embrapa Agropecuária Oeste; Embrapa Amapá; Embrapa Amazônia Oriental; Embrapa Clima Temperado; Embrapa Mandioca e Fruticultura; Embrapa Meio Ambiente; Embrapa Meio Norte / UEP-Parnaíba; Embrapa Meio-Norte; Embrapa Pantanal... Mostrar Todas |
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Registros recuperados : 18 | |
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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: |
07/04/1994 |
Data da última atualização: |
16/11/2023 |
Autoria: |
PORTO. M. C. M. |
Afiliação: |
EMBRAPA-CNPMF. |
Título: |
Physiological mechanisms of drought tolerance in cassava (Manihot esculenta Crantz). |
Ano de publicação: |
1983 |
Fonte/Imprenta: |
Arizona: University of Arizona, 1983. |
Páginas: |
114p. |
Série: |
Tese Doutorado |
Idioma: |
Inglês |
Conteúdo: |
The response of cassava (Manihot esculenta Crantz) to water stress was evaluated in two experiments conducted in Tucson, Arizona and Santander de Quilichao, Colombia, involving five cultivars (Mven 218, CMC 40, MCol 22, Mita 1158 and MCol 1684). In both experiments stress was imposed in a given stage of the plant cycle. A third experiment, conducted in Palmira, Colombia, evaluated the relationship existng between photosynthesis, relative humidity and yields of cassava. Cultivar MCol 1684 reduced its transpirating area by either reducing leaf formation (stress given to 3-month-old plants) or increasing leaf fall (6-month-old plants). A reduction in plant growth and leaf expansion rates is attributed to reducing the plant's total leaf area. Water stress imposed in Tucson also showed reductions in plant growth, leaf formation, extension and final leaf size (except for MVen 218). Plants of MCol 1684 in Santander de Quilichao, like MVen 218 in Tucson, did not change their final leaf leaf sizes due to stress. Dry matter production was more reduced when stress was imposed early in the plant growth cycle. Dry matter partitioning was also altered by stress given to 3-month-old plants of MCol 1684. The stressed plants delayed the allocation of dry matter to the storage roots. Noon and afternoon values of leaf coductance and transpiration of MCol 1684 were reduced after 40 days of stress. Interestingly, leaf temperatures of non-stressed plants were higher than those of the stressed plants. This can be attributed to an increase in leaf reflectance in the stressed plants by changing the angle of orientation of their leaves in relation to the sun. Leaf coductances of non-stressed plants were correlated to photosynthesis, leaf temperatures and vapor pressure deficits in measurements taken at 3:00 PM. In the stressed plants conductances were also correlated to photosynthesis leaf temperatures, air moisture and transpiration. Leaf water potentials were slightly reduced by stress in Tucson, except for MVen 218. Plants of MCol 1684, in Quilichao, did not show significant reduction in L due to stress. In contrast, noon and mid-afternoon values of L were lower in the non-stressed plants after 30-40 days of treatment. This suggests the occurrence of higher daily water stresses in non-stressed plants, because of elevated transpiration rates. The effect of air humidity on the stomatal functioning of MCol 1684 seems to be strong, as proved the dependence of transpiration, conductances and photosynthesis on relative humidity. MenosThe response of cassava (Manihot esculenta Crantz) to water stress was evaluated in two experiments conducted in Tucson, Arizona and Santander de Quilichao, Colombia, involving five cultivars (Mven 218, CMC 40, MCol 22, Mita 1158 and MCol 1684). In both experiments stress was imposed in a given stage of the plant cycle. A third experiment, conducted in Palmira, Colombia, evaluated the relationship existng between photosynthesis, relative humidity and yields of cassava. Cultivar MCol 1684 reduced its transpirating area by either reducing leaf formation (stress given to 3-month-old plants) or increasing leaf fall (6-month-old plants). A reduction in plant growth and leaf expansion rates is attributed to reducing the plant's total leaf area. Water stress imposed in Tucson also showed reductions in plant growth, leaf formation, extension and final leaf size (except for MVen 218). Plants of MCol 1684 in Santander de Quilichao, like MVen 218 in Tucson, did not change their final leaf leaf sizes due to stress. Dry matter production was more reduced when stress was imposed early in the plant growth cycle. Dry matter partitioning was also altered by stress given to 3-month-old plants of MCol 1684. The stressed plants delayed the allocation of dry matter to the storage roots. Noon and afternoon values of leaf coductance and transpiration of MCol 1684 were reduced after 40 days of stress. Interestingly, leaf temperatures of non-stressed plants were higher than those of the stressed pla... Mostrar Tudo |
Palavras-Chave: |
Drought resistance; Estados Unidos; Estresse hidrico; Palmira; Plant water relations; Quilichao; Relative umidity; Tolerancia a seca; Tucson; Whater stress. |
Thesagro: |
Deficiência Hídrica; Fisiologia; Fotossíntese; Mandioca; Manihot Esculenta; Matéria Seca; Produtividade; Relação Água-Planta; Resistência a Seca; Umidade Relativa. |
Thesaurus NAL: |
Arizona; cassava; Colombia; drought tolerance; dry matter content; Manihot; photosynthesis; physiology; United States; yields. |
Categoria do assunto: |
-- F Plantas e Produtos de Origem Vegetal |
Marc: |
LEADER 03829nam a2200493 a 4500 001 1651391 005 2023-11-16 008 1983 bl uuuu m 00u1 u #d 100 1 $aPORTO. M. C. M. 245 $aPhysiological mechanisms of drought tolerance in cassava (Manihot esculenta Crantz). 260 $aArizona: University of Arizona$c1983 300 $a114p. 490 $aTese Doutorado 520 $aThe response of cassava (Manihot esculenta Crantz) to water stress was evaluated in two experiments conducted in Tucson, Arizona and Santander de Quilichao, Colombia, involving five cultivars (Mven 218, CMC 40, MCol 22, Mita 1158 and MCol 1684). In both experiments stress was imposed in a given stage of the plant cycle. A third experiment, conducted in Palmira, Colombia, evaluated the relationship existng between photosynthesis, relative humidity and yields of cassava. Cultivar MCol 1684 reduced its transpirating area by either reducing leaf formation (stress given to 3-month-old plants) or increasing leaf fall (6-month-old plants). A reduction in plant growth and leaf expansion rates is attributed to reducing the plant's total leaf area. Water stress imposed in Tucson also showed reductions in plant growth, leaf formation, extension and final leaf size (except for MVen 218). Plants of MCol 1684 in Santander de Quilichao, like MVen 218 in Tucson, did not change their final leaf leaf sizes due to stress. Dry matter production was more reduced when stress was imposed early in the plant growth cycle. Dry matter partitioning was also altered by stress given to 3-month-old plants of MCol 1684. The stressed plants delayed the allocation of dry matter to the storage roots. Noon and afternoon values of leaf coductance and transpiration of MCol 1684 were reduced after 40 days of stress. Interestingly, leaf temperatures of non-stressed plants were higher than those of the stressed plants. This can be attributed to an increase in leaf reflectance in the stressed plants by changing the angle of orientation of their leaves in relation to the sun. Leaf coductances of non-stressed plants were correlated to photosynthesis, leaf temperatures and vapor pressure deficits in measurements taken at 3:00 PM. In the stressed plants conductances were also correlated to photosynthesis leaf temperatures, air moisture and transpiration. Leaf water potentials were slightly reduced by stress in Tucson, except for MVen 218. Plants of MCol 1684, in Quilichao, did not show significant reduction in L due to stress. In contrast, noon and mid-afternoon values of L were lower in the non-stressed plants after 30-40 days of treatment. This suggests the occurrence of higher daily water stresses in non-stressed plants, because of elevated transpiration rates. The effect of air humidity on the stomatal functioning of MCol 1684 seems to be strong, as proved the dependence of transpiration, conductances and photosynthesis on relative humidity. 650 $aArizona 650 $acassava 650 $aColombia 650 $adrought tolerance 650 $adry matter content 650 $aManihot 650 $aphotosynthesis 650 $aphysiology 650 $aUnited States 650 $ayields 650 $aDeficiência Hídrica 650 $aFisiologia 650 $aFotossíntese 650 $aMandioca 650 $aManihot Esculenta 650 $aMatéria Seca 650 $aProdutividade 650 $aRelação Água-Planta 650 $aResistência a Seca 650 $aUmidade Relativa 653 $aDrought resistance 653 $aEstados Unidos 653 $aEstresse hidrico 653 $aPalmira 653 $aPlant water relations 653 $aQuilichao 653 $aRelative umidity 653 $aTolerancia a seca 653 $aTucson 653 $aWhater stress
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