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| Acceso al texto completo restringido a Biblioteca INIA Las Brujas. Por información adicional contacte bibliolb@inia.org.uy. |
Registro completo
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Biblioteca (s) : |
INIA Las Brujas. |
Fecha : |
15/10/2014 |
Actualizado : |
10/02/2020 |
Tipo de producción científica : |
Artículos en Revistas Indexadas Internacionales |
Autor : |
CAMPI, P.; GARCIA, C. |
Afiliación : |
CLAUDIO CESAR GARCIA GALLARRETA, Instituto Nacional de Investigación Agropecuaria (INIA), Uruguay. |
Título : |
Effects of irrigation management and nitrogen fertilization on the yield and quality of 'Gala' apple. |
Fecha de publicación : |
2011 |
Fuente / Imprenta : |
Acta Horticulturae, 2011, no.889, p.249-256. |
Serie : |
(Acta Horticulturae; 889) |
ISSN : |
0567-7572 |
DOI : |
10.17660/ActaHortic.2011.889.29 |
Idioma : |
Inglés |
Notas : |
Article history: November 2, 2009. In: Acta Horticulturae (ISHS) 889: VI International Symposium on Irrigation of Horticultural Crops. Editors: S. Ortega-Farias, G. Selles.
Location: Viña del Mar (Chile). Begin date: November 2, 2009. End date: November 6, 2009. |
Contenido : |
ABSTRACT.
Fertilizers application in irrigation water (Fertigation) is considered to be an efficient method of fertilizing fruit trees, but some information is needed on the relationship between irrigation depth and nitrogen (N). The objective of this work was to know the response of apple tree to different levels of irrigation depth based on maximum crop evapotranspiration (ET c) and N fertilization. The experiment was carried out in 2008-09 summer growing season of apple trees Malus x domestica Borkh 'Gala', with a row spacing of 4×1 m (2500 pl. ha -1), seven years old, on the M9 rootstock, in a silt loam soil. The experimental design was split plots with two factors, with four complete randomized blocks. A main plot was irrigation depth according ET c: 0% (only rainfall), 50, 75 and 100% of the ET c, and a submain plot was three N fertilization levels: 0, 110 and 220 kg N ha -1. Soil water content (0-20 cm of soil depth), leaf minerals content (N, P, K, Ca, Mg), trunk section diameter, fruit total number, fruit diameter, weight, colour and firmness were measured. Different leaf mineral contents for N, K and P according irrigation depth were observed at pre-harvest. Nitrogen fertilization, however, only affected the leaf N content. Results indicate that it was a significant differences in yield, fruit diameter and weight response to the supplemental irrigation application. Yield for irrigation at 100% ET c, reached 40 t ha -1 and, for non-irrigation plants 27 t ha -1. Fruit diameters average was 71.53 and 62.69 mm for 100% ET c and non-irrigation treatments, respectively; and there were 70.97 and 67.88 mm for 220 kg N ha -1 and non-nitrogen treatments respectively. The differences in N fertilization on yield and fruit quality variables were not observed. Nitrogen application rates only affected fruit diameter but not yield. MenosABSTRACT.
Fertilizers application in irrigation water (Fertigation) is considered to be an efficient method of fertilizing fruit trees, but some information is needed on the relationship between irrigation depth and nitrogen (N). The objective of this work was to know the response of apple tree to different levels of irrigation depth based on maximum crop evapotranspiration (ET c) and N fertilization. The experiment was carried out in 2008-09 summer growing season of apple trees Malus x domestica Borkh 'Gala', with a row spacing of 4×1 m (2500 pl. ha -1), seven years old, on the M9 rootstock, in a silt loam soil. The experimental design was split plots with two factors, with four complete randomized blocks. A main plot was irrigation depth according ET c: 0% (only rainfall), 50, 75 and 100% of the ET c, and a submain plot was three N fertilization levels: 0, 110 and 220 kg N ha -1. Soil water content (0-20 cm of soil depth), leaf minerals content (N, P, K, Ca, Mg), trunk section diameter, fruit total number, fruit diameter, weight, colour and firmness were measured. Different leaf mineral contents for N, K and P according irrigation depth were observed at pre-harvest. Nitrogen fertilization, however, only affected the leaf N content. Results indicate that it was a significant differences in yield, fruit diameter and weight response to the supplemental irrigation application. Yield for irrigation at 100% ET c, reached 40 t ha -1 and, for non-irrigation plants 27 t ha -1. Fru... Presentar Todo |
Palabras claves : |
Evapotranspiration; Growing fruit; Irrigation depth; Malus x domestica; Nitrate. |
Thesagro : |
EVAPOTRANSPIRACIÓN; MANZANA; RIEGO. |
Asunto categoría : |
F06 Riego |
Marc : |
LEADER 02913naa a2200277 a 4500 001 1051110 005 2020-02-10 008 2011 bl uuuu u00u1 u #d 022 $a0567-7572 024 7 $a10.17660/ActaHortic.2011.889.29$2DOI 100 1 $aCAMPI, P. 245 $aEffects of irrigation management and nitrogen fertilization on the yield and quality of 'Gala' apple.$h[electronic resource] 260 $c2011 490 $a(Acta Horticulturae; 889) 500 $aArticle history: November 2, 2009. In: Acta Horticulturae (ISHS) 889: VI International Symposium on Irrigation of Horticultural Crops. Editors: S. Ortega-Farias, G. Selles. Location: Viña del Mar (Chile). Begin date: November 2, 2009. End date: November 6, 2009. 520 $aABSTRACT. Fertilizers application in irrigation water (Fertigation) is considered to be an efficient method of fertilizing fruit trees, but some information is needed on the relationship between irrigation depth and nitrogen (N). The objective of this work was to know the response of apple tree to different levels of irrigation depth based on maximum crop evapotranspiration (ET c) and N fertilization. The experiment was carried out in 2008-09 summer growing season of apple trees Malus x domestica Borkh 'Gala', with a row spacing of 4×1 m (2500 pl. ha -1), seven years old, on the M9 rootstock, in a silt loam soil. The experimental design was split plots with two factors, with four complete randomized blocks. A main plot was irrigation depth according ET c: 0% (only rainfall), 50, 75 and 100% of the ET c, and a submain plot was three N fertilization levels: 0, 110 and 220 kg N ha -1. Soil water content (0-20 cm of soil depth), leaf minerals content (N, P, K, Ca, Mg), trunk section diameter, fruit total number, fruit diameter, weight, colour and firmness were measured. Different leaf mineral contents for N, K and P according irrigation depth were observed at pre-harvest. Nitrogen fertilization, however, only affected the leaf N content. Results indicate that it was a significant differences in yield, fruit diameter and weight response to the supplemental irrigation application. Yield for irrigation at 100% ET c, reached 40 t ha -1 and, for non-irrigation plants 27 t ha -1. Fruit diameters average was 71.53 and 62.69 mm for 100% ET c and non-irrigation treatments, respectively; and there were 70.97 and 67.88 mm for 220 kg N ha -1 and non-nitrogen treatments respectively. The differences in N fertilization on yield and fruit quality variables were not observed. Nitrogen application rates only affected fruit diameter but not yield. 650 $aEVAPOTRANSPIRACIÓN 650 $aMANZANA 650 $aRIEGO 653 $aEvapotranspiration 653 $aGrowing fruit 653 $aIrrigation depth 653 $aMalus x domestica 653 $aNitrate 700 1 $aGARCIA, C. 773 $tActa Horticulturae, 2011, no.889, p.249-256.
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| Acceso al texto completo restringido a Biblioteca INIA Las Brujas. Por información adicional contacte bibliolb@inia.org.uy. |
Registro completo
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Biblioteca (s) : |
INIA Las Brujas. |
Fecha actual : |
01/11/2021 |
Actualizado : |
01/11/2021 |
Tipo de producción científica : |
Capítulo en Libro Técnico-Científico |
Autor : |
FERREIRA, V.; GONZÁLEZ-ARCOS, M.; PIANZZOLA, M.J.; COLL, N.S.; SIRI, M.I.; VALLS, M. |
Afiliación : |
VIRGINIA FERREIRA, Área Microbiología, Departamento de Biociencias (DEPBIO), Facultad de Química, Universidad de la República, Montevideo, Uruguay; MATIAS GONZÁLEZ-ARCOS, INIA (Instituto Nacional de Investigación Agropecuaria), Uruguay; MARÍA JULIA PIANZZOLA, Área Microbiología, Departamento de Biociencias (DEPBIO), Facultad de Química, Universidad de la República, Montevideo, Uruguay; NÚRIA S. COLL, Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain; MARÍA INÉS SIRI, Área Microbiología, Departamento de Biociencias (DEPBIO), Facultad de Química, Universidad de la República, Montevideo, Uruguay; MARC VALLS, Centre for Research in Agricultural Genomics (CSIC-IRTA-UAB-UB), Bellaterra, Catalonia, Spain; Department of Genetics, University of Barcelona, Bellaterra, Catalonia, Spain. |
Título : |
Molecular detection of Ralstonia solanacearum to facilitate breeding for resistance to bacterial wilt in potato. |
Fecha de publicación : |
2021 |
Fuente / Imprenta : |
In: Dobnik D., Gruden K., Ram?ak ?., Coll A. (eds). Solanum tuberosum. Methods in Molecular Biology, 2021, vol 2354. Humana, New York, NY. doi: https://doi.org/10.1007/978-1-0716-1609-3_18 |
Serie : |
eBook Packages Springer Protocols, (Methods in Molecular Biology, volume 2354). |
ISBN : |
978-1-0716-1608-6 (print) / 978-1-0716-1609-3 (e-book) |
ISSN : |
1064-3745 (print) / 1940-6029 (electronic) |
DOI : |
10.1007/978-1-0716-1609-3_18 |
Idioma : |
Inglés |
Notas : |
Article history: First Online 27 August 2021. |
Contenido : |
ABSTRACT. - Potato bacterial wilt is caused by the devastating bacterial pathogen Ralstonia solanacearum. Quantitative resistance to this disease has been and is currently introgressed from a number of wild relatives into cultivated varieties through laborious breeding programs. Here, we present two methods that we have developed to facilitate the screening for resistance to bacterial wilt in potato. The first one uses R. solanacearum reporter strains constitutively expressing the luxCDABE operon or the green fluorescent protein (gfp) to follow pathogen colonization in potato germplasm. Luminescent strains are used for nondestructive live imaging, while fluorescent ones enable precise pathogen visualization inside the plant tissues through confocal microscopy. The second method is a BIO-multiplex-PCR assay that is useful for sensitive and specific detection of viable R. solanacearum (IIB-1) cells in latently infected potato plants. This BIO-multiplex-PCR assay can specifically detect IIB-1 sequevar strains as well as strains belonging to all four R. solanacearum phylotypes and is sensitive enough to detect without DNA extraction ten bacterial cells per mL in complex samples. The described methods allow the detection of latent infections in roots and stems of asymptomatic plants and were shown to be efficient tools to assist potato breeding programs. © 2021, Springer Science+Business Media, LLC, part of Springer Nature. |
Palabras claves : |
Bacterial wilt; Disease resistance; Plant breeding; Potato brown rot; Ralstonia solanacearum; Solanum tuberosum. |
Asunto categoría : |
F30 Genética vegetal y fitomejoramiento |
Marc : |
LEADER 02607naa a2200301 a 4500 001 1062509 005 2021-11-01 008 2021 bl uuuu u00u1 u #d 022 $a1064-3745 (print) / 1940-6029 (electronic) 024 7 $a10.1007/978-1-0716-1609-3_18$2DOI 100 1 $aFERREIRA, V. 245 $aMolecular detection of Ralstonia solanacearum to facilitate breeding for resistance to bacterial wilt in potato.$h[electronic resource] 260 $c2021 490 $aeBook Packages Springer Protocols, (Methods in Molecular Biology, volume 2354). 500 $aArticle history: First Online 27 August 2021. 520 $aABSTRACT. - Potato bacterial wilt is caused by the devastating bacterial pathogen Ralstonia solanacearum. Quantitative resistance to this disease has been and is currently introgressed from a number of wild relatives into cultivated varieties through laborious breeding programs. Here, we present two methods that we have developed to facilitate the screening for resistance to bacterial wilt in potato. The first one uses R. solanacearum reporter strains constitutively expressing the luxCDABE operon or the green fluorescent protein (gfp) to follow pathogen colonization in potato germplasm. Luminescent strains are used for nondestructive live imaging, while fluorescent ones enable precise pathogen visualization inside the plant tissues through confocal microscopy. The second method is a BIO-multiplex-PCR assay that is useful for sensitive and specific detection of viable R. solanacearum (IIB-1) cells in latently infected potato plants. This BIO-multiplex-PCR assay can specifically detect IIB-1 sequevar strains as well as strains belonging to all four R. solanacearum phylotypes and is sensitive enough to detect without DNA extraction ten bacterial cells per mL in complex samples. The described methods allow the detection of latent infections in roots and stems of asymptomatic plants and were shown to be efficient tools to assist potato breeding programs. © 2021, Springer Science+Business Media, LLC, part of Springer Nature. 653 $aBacterial wilt 653 $aDisease resistance 653 $aPlant breeding 653 $aPotato brown rot 653 $aRalstonia solanacearum 653 $aSolanum tuberosum 700 1 $aGONZÁLEZ-ARCOS, M. 700 1 $aPIANZZOLA, M.J. 700 1 $aCOLL, N.S. 700 1 $aSIRI, M.I. 700 1 $aVALLS, M. 773 $tIn: Dobnik D., Gruden K., Ram?ak ?., Coll A. (eds). Solanum tuberosum. Methods in Molecular Biology, 2021, vol 2354. Humana, New York, NY. doi: https://doi.org/10.1007/978-1-0716-1609-3_18
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