Ocorrência de Fusarium oxysporum f. sp. lycopersici raça 3 em tomate no Brasil e seleção de novas fontes de resistência ao patógeno.

A murcha-de-fusário, causada por Fusarium oxysporum f. sp. lycopersici (FOL), é uma importante doença do tomateiro (Lycopersicon esculentum Mill.) no mundo. Existem três raças identificadas do patógeno, sendo que a raça 3 ainda não havia sido registrada no Brasil. Este trabalho teve dois objetivos: comunicar a presença da raça 3 de FOL no Brasil e selecionar fontes de resistência às três raças do patógeno. Nove isolados de FOL foram obtidos de dois híbridos de tomate (Carmen e Alambra) com sintomas de mrucha, provenientes de três lavouras localizadas nos municípios de Venda Nova do Imigrante - Espírito Santo e Domingos Martins 9ES). Estes dois híbridos comerciais de tomate são considerados resistentes ás raças 1 e 2 de FOL. O teste de virul��ncia foi feito com as cultivares: Ponderosa (suscetível a todasa as raças), IPA-5 (resistente à raça 1), Floradade (resistente às raças 1 e 2) e BHRS-2,3 (resistente às raças 1, 2 e 3). Todos os isolados foram virulentos às cultivares Ponderosa, IPA-R e Floradade e ainda infectaram algumas plantas de BHRS-2,3. O teste de virul��ncia foi repetido com as mesmas cultivares mas também incluindo o acesso 'LA 716' da espécie selvagem L. pennellii. Foram obtidos resultados semelhantes para as cultivares, enquanto L. pennellii apresentou uma reação de imunidade ao patógeno. Estes resultadaos comprovam que os novos isolados de ES pertencem à raça 3 de FOL. Uma coleção de germoplasma de acessos de Lycopersicon spp. da Embrapa Hortaliças foi inicialmente avaliada quanto à reação de um dos isolados da raça 3 e uma parte deles às raças 1 e 2. Novas fontes de resistência múltipla foram identificadas em acessos de L. chilense, l. hirsutum e L. peruvianum, sendo dez genótipos imunes às raças 2 e 3 e cinco às três raças. A identificação destas fontes de resistência peermite que os programas de melhoramento de tomate antecipem potenciais problemas, inclusive a emergência de novas raças de FOL, al��m das raças 1, 2 e 3.

Resistência de acessos de Lycopersicon a Stemphylium solani e S. lycopersici.

A mancha-de-estenfílio, causada por Stemphylium solani e/ou S. lycopersici, é uma conhecida doença do tomateiro que voltou a ser importante, principalmente porque os atuais híbridos plantados no país não apresentam resistência. O controle da mancha-de-estenfílio se baseia no uso de cultivares resistentes ou outras medidas de manejo como o controle químico e a rotação de cultura. Este trabalho teve como objetivo selecionar novas fontes de resistência à doença in Lycopersicon. Entre os acessos de Lycopersicon avaliados para resistência 18 (54,5%) comportaram-se como suscetíveis, três (9,1%) comportaram-se como intermediários e 12 (36,4%) foram resistentes para as duas espécies fúngicas. Todos os acessos resistentes a S. solani também foram resistentes a S. lycopersici. Foram identificados acessos resistentes e intermediários nas espécies L. esculentum (muito provavelmente portando o gene Sm), L. peruvianum e L. hirsutum.

Microscopia eletrônica de varredura da interação Alternaria solani - tomateiro suscetível e resistente.

Objetivando analisar os eventos iniciais das interações A. solani - L. hirsutum var. glabratum e A. solani - L. esculentum ev. Miller, será realizado um trabalho utilizando processamento para microscopia eletrônica de varredura.

Resistência de genótipos de tomateiro ao ácaro rajado

Avaliou-se a resistência de genótipos de tomateiro selvagens [Lycopersicon pennellii (LA 716), L. hirsutum var. glabratum (PI 126449, PI 134417), L. hirsutum (PI 127826, PI 127827), L. peruvianum (CGO 6707), L. peruvianum var. dentatum (WYR 2020, LA 111), L. peruvianum var. glandulosum (LA 1113-1, LA 1113-2)] e comerciais [(L. esculentum) Gem Pride, Santa Clara, e híbridos Bruna VFN, Carmem, Fortaleza, Débora Plus VFN] ao ácaro rajado (Tetranychus urticae). O número médio de ovos, fases imaturas (larvas, protoninfas e deutoninfas) e adultos por fol��olo foi contado; o índice de preferência para oviposição (IPO) foi calculado. O delineamento experimental foi blocos ao acaso, com 6 repetições. Os genótipos LA 716, PI 126449, PI 134417, PI 127827, PI 127826 e Gem Pride apresentaram não-preferência para oviposição do ácaro rajado, sendo deterrentes quanto à classificação do IPO, enquanto os genótipos LA 111, WYR 2020, LA 1113-2 e LA1113-1 foram os mais preferidos para a oviposição e foram considerados como estimulantes pelo IPO.

Nonpreference of whitefly for oviposition in tomato genotypes

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Tipos de tricomas em genótipos de Lycopersicon

Fundação de Amparo à Pesquisa do Estado de São Paulo (FAPESP)

Improving the affinity of tomato grafted on Solanum torvum using an intermediate rootstock

Most of the interspecific rootstocks (Lycopersicum esculentum × L. hirsutum) used in grafted Spanish tomato crops are resistant to Meloidogyne nematodes, but the 'Mi' resistance gene does not work well at high soil temperatures. Ralstonia solanacearum is a bacterial disease usual in tropical areas, but recently identified with low incidence in several European countries. This disease could be controlled by grafting tomato on Solanum torvum, which is also resistant to Meloidogyne. However, S. torvum and tomato have low grafting affinity, which could be improved using an intermediate rootstock. Some cultivars of eggplant have a relatively good affinity with tomato and complete affinity with S. torvum. In this study we compared two tomato cultivars (one resistant to Verticillium dalihae, Fusarium oxysporum v. lycopersici race 2 and Meloidogyne spp., and one non-resistant) grafted onto 'Beaufort' (Lycopersicum esculentum × L. hirsutum), 'Torvum Vigor' (Solanum torvum) and also with an intermediate grafting of eggplant ('Cristal') between tomato and S. torvum, with nongrafted plants as controls. This arrangement was carried out in two cropping cycles (winter-spring and summer-autumn). In both cycles, plants grafted onto S. torvum, both single or double grafted, yielded less than those grafted onto 'Beaufort' or nongrafted plants. In the spring cycle, no differences were found between single and double-grafted plants using S. torvum rootstocks, but in the autumn cycle double grafted plants had higher yields than the single grafted plants. The severity of nematode infections, in terms of reducing yields, and/or hypothetical infections of Ralstonia, will determine the utility of this technique in tomato production.

Ancient origin of pathogen recognition specificity conferred by the tomato disease resistance gene Pto

We have investigated the origin of the Pto disease resistance (R) gene that was previously identified in the wild tomato species Lycopersicon pimpinellifolium and isolated by map-based cloning. Pto encodes a serine-threonine protein kinase that specifically recognizes strains of Pseudomonas syringae pv. tomato (Pst) that express the avirulence gene avrPto. We examined an accession of the distantly related wild species Lycopersicon hirsutum var. glabratum that exhibits avrPto-specific resistance to Pst. The Pst resistance of L. hirsutum was introgressed into a susceptible Lycopersicon esculentum background to create the near-isogenic line 96T133-3. Resistance to Pst(avrPto) in 96T133-3 was inherited as a single dominant locus and cosegregated with a restriction fragment length polymorphism detected by the Pto gene. This observation suggested that a member of the Pto gene family confers Pst(avrPto) resistance in this L. hirsutum line. Here we report the cloning and characterization of four members of the Pto family from 96T133-3. One gene (LhirPto) is 97% identical to Pto and encodes a catalytically active protein kinase that elicits a hypersensitive response when coexpressed with avrPto in leaves of Nicotiana benthamiana. In common with the Pto kinase, the LhirPto protein physically interacts with AvrPto and downstream members of the Pto signaling pathway. Our studies indicate that R genes of the protein kinase class may not evolve rapidly in response to pathogen pressure and rather that their ability to recognize specific Avr proteins can be highly conserved.

Nitrous oxide emissions from fertilized, irrigated cotton (Gossypium hirsutum L.) in the Aral Sea Basin, Uzbekistan : influence of nitrogen applications and irrigation practices

Nitrous oxide emissions were monitored at three sites over a 2-year period in irrigated cotton fields in Khorezm, Uzbekistan, a region located in the arid deserts of the Aral Sea Basin. The fields were managed using different fertilizer management strategies and irrigation water regimes. N2O emissions varied widely between years, within 1 year throughout the vegetation season, and between the sites. The amount of irrigation water applied, the amount and type of N fertilizer used, and topsoil temperature had the greatest effect on these emissions. Very high N2O emissions of up to 3000 μg N2O-N m−2 h−1 were measured in periods following N-fertilizer application in combination with irrigation events. These “emission pulses” accounted for 80–95% of the total N2O emissions between April and September and varied from 0.9 to 6.5 kg N2O-N ha−1.. Emission factors (EF), uncorrected for background emission, ranged from 0.4% to 2.6% of total N applied, corresponding to an average EF of 1.48% of applied N fertilizer lost as N2O-N. This is in line with the default global average value of 1.25% of applied N used in calculations of N2O emissions by the Intergovernmental Panel on Climate Change. During the emission pulses, which were triggered by high soil moisture and high availability of mineral N, a clear diurnal pattern of N2O emissions was observed, driven by daily changes in topsoil temperature. For these periods, air sampling from 8:00 to 10:00 and from 18:00 to 20:00 was found to best represent the mean daily N2O flux rates. The wet topsoil conditions caused by irrigation favored the production of N2O from NO3− fertilizers, but not from NH4+ fertilizers, thus indicating that denitrification was the main process causing N2O emissions. It is therefore argued that there is scope for reducing N2O emission from irrigated cotton production; i.e. through the exclusive use of NH4+ fertilizers. Advanced application and irrigation techniques such as subsurface fertilizer application, drip irrigation and fertigation may also minimize N2O emission from this regionally dominant agro-ecosystem.

Stunted cotton (Gossypium hirsutum L.) fully recovers biomass and yield of seed cotton after delayed root inoculation with spores of an arbuscular mycorrhizal fungus (Glomus mosseae)

In the northern grain and cotton region of Australia, poor crop growth after long periods of fallow, called 'long-fallow' disorder, is caused by a decline of natural arbuscular-mycorrhizal fungi (AMF). When cotton was grown in large pots containing 22 kg of Vertisol from a field recently harvested from cotton in Central Queensland, plants in pasteurised soil were extremely stunted compared with plants in unpasteurised soil. We tested the hypothesis that this extreme stunting was caused by the absence of AMF and examined whether such stunted plants could recover from subsequent treatment with AMF spores and/or P fertiliser. At 42 days after sowing, the healthy cotton growing in unpasteurised soil had 48% of its root-length colonised with AMF, whereas the stunted cotton had none. After inoculation with AMF spores (6 spores/g soil of Glomus mosseae) and/or application of P fertiliser (50 mg P/kg soil) at 45 days after sowing, the stunted plants commenced to improve about 25 days after treatment, and continued until their total dry matter and seed cotton production equalled that of plants growing in unpasteurised soil with natural AMF. In contrast, non-mycorrhizal cotton grown without P fertiliser remained stunted throughout and produced no bolls and only 1% of the biomass of mycorrhizal cotton. Even with the addition of P fertiliser, non-mycorrhizal cotton produced only 64% of the biomass and 58% of the seed cotton (lint + seed) of mycorrhizal cotton plants. These results show that cotton is highly dependent on AMF for P nutrition and growth in Vertisol (even with high rates of P fertiliser), but can recover from complete lack of AMF and consequent stunting during at least the first 45 days of growth when treated with AMF spores and/or P fertiliser. This corroborates field observations in the northern region that cotton may recover from long-fallow disorder caused by low initial levels of AMF propagules in the soil as the AMF colonisation of its roots increases during the growing season.

Efecto de rotación de cultivos y métodos de control de malezas sobre la cenosis de las malezas y el crecimiento, desarrollo y rendimiento de los cultivos de soya (Glycine max (L) Merr.) c.v Cristalina y algodón (Gossypium hirsutum) c.v H 373

Se determinó la influencia de las prácticas de rotación de cultivos y control de malezas sobre la dinámica de las malezas, y el crecimiento, desarrollo y rendimiento en el cultivo de Soya y Algodón, en terrenos del Centro Experimental del Algodón, ubicado en el municipio de Posoltega, Departamento de Chinandega, se estableció el presente ensayo durante la época de postrera de Agosto 1991 a Enero 1992. Se utilizó un diseño bifactorial en parcelas divididas en bloques completamente al azar con cuatro repeticiones siendo los factores en estudios los siguientes: Factor A: Rotación de cultivos (Soya sin inocular-Algodón, soya inoculada-algodón, soya inocutada-soya inoculada, soya sin inocular-soya sin inocular, Ajonjol��-Algodón.) Factor B: Métodos de control de malezas (Control químico, control período crítico, control limpia periódica.). Las rotaciones de soya redujeron la abundancia total de malezas predominando la especie Desmodiun canum. La menor cobertura y menor biomasa fue reflejada por la rotación Soya sin inocular-Soya sin inocular, no obstante la menor diversidad se encontró en la rotación Soya inoculada-Soya inoculada. El control limpia periódica disminuyó la cobertura y abundancia, pero presentó una biomasa intermedia respecto a los otros controles y una diversidad similar. En el cultivo de soya para la variable de altura de planta, diámetro de tallo, número de nódulos por planta y número de nudos no existen diferencias significativas, lo mismo para las variables de rendimientos. En el cultivo del algodón se obtuvo diferencias significativas para las variables de crecimiento y rendimiento. En cuanto a las variables de crecimiento y rendimiento la rotación ajonjol��-algodón reflejó los siguientes valores diámetro de tallo (4.1 mm), altura de planta (134.0 cm), rendimiento Kg/ha (1758). La rotación Soya sin inocular-Soya sin inocular reflejó diámetro de tallo (4.3 mm). altura de planta (65.7 cm) y rendimiento de 1553 kg/ha registrando los mejores resultados.

Periodos criticos de competencia de malezas en algodon (Gossypium hirsutum L.)

Este estudio fue realizado en el Centro experimental de Algodón (C.E.A), Nicaragua; con el propósito de determinar el periodo crítico de competencia en algodón (Gossypium hirsutum L.) y las malezas. Dos experimentos fueron sembrados en agosto de 1991. En el experimento 1 (períodos libres de malezas) los tratamientos, 7 en total, consistieron en mantener parcelas libres de malezas desde la siembra hasta 14, 28, 42, 56, 70 días después de la siembra. Un tratamiento fue dejado enmalezado durante todo el ciclo y otro fue dejado libre de maleza. En el experimento 2 (períodos con competencia) a las malezas les fue permitido competir por diferentes períodos comenzando los controles a los 14, 28, 42, 56 y 70 días después de la siembra. un tratamiento fue dejado enmalezado durante todo el ciclo y otro fue dejado libre de maleza. Los resultados obtenidos muestran que bajo las condiciones experimentales, el algodón necesita 70 días libres de malezas para obtener buenos rendimientos y es capaz de soportar 42 días de competencia sin ver mermado sus rendimientos de manera significativa. El período crítico de competencia encuentra entre 42 y 70 días después de la siembra. El mejor resultado fue obtenido cuando las malezas fueron controladas en dos ocasiones, la primera 42 días después de la siembra y la segunda 70 días después de la siembra.

Influencia de diferentes cultivos antecedentes y métodos de control de malezas sobre la cenosis: el crecimiento, desarrollo y rendimiento del algodonero (Gossypium hirsutum L.) var. CEA H-373

Durante el ciclo agrícola 1988 -1989 en el centro experimental del Algodón Ubicado en la localidad de Posooltega, Chinandega se realizó un estudio con el propósito de determinar la influencia de diferentes cultivos antecedentes y métodos de control de malezas a la dinámica de las malezas y al crecimiento, desarrollo y rendimiento del cultivo del algodonero; utilizando la variedad CEA H 373.. se utilizo el diseño de parcelas divididas en bloques al azar con cuatro repeticiones y nueve tratamientos los cuales corresponden a las combinaciones de tres antecesores con tres métodos de control de malezas: se usaron los cultivos antecesores Soya sin inoculación (al), Soya inoculada (a2), Ajonjol�� (a3) y los métodos de control Fluometuron 1425 cc de i.a./ha mas una limpia (b1), 2, limpia (b2) y limpias repetidas(b3). No se encontraron diferentes significativas en la influencia de los cultivos antecesores Soya sin inoculación (a1), se exibe una menor abundancia total de malezas, menor cobertura y menor biomasa permitiendo al cultivo un mejor comportamiento en su crecimiento y desarrollo. Contrario a esto el cultivo antecesor Soya sin inoculada (a2) manifestó el menor rendimiento, mayor cobertura y una abundancia total y biomasa de malezas superadas tan solo ligeramente por la originada en la influencia del cultivo antecesor Ajonjol�� (a3). No hubo diferencias sustanciales en la diversidad de malezas por efecto de los diferentes cultivos procedentes como de los métodos de control de malezas. Se logró de terminar que hubo diferencias significativas en el rendimiento del algodonero en los métodos de control de malezas resultando los métodos de control químico (b1) y limpias periódicas (b3) los de mejor comportamiento. Con las limpias periódicas (b3) se produce la menor abundancia total de malezas menor a cobertura y menor biomasa. Opuesto a estos resultados, el método de una sola limpia (b2) origino la mayor abundancia total, y mayor cobertura de malezas. Al mismo tiempo este mismo método (b2) presento los menores valores para las variables de rendimientos de algodonero. Finalmente el rendimiento del algodonero se vio influenciado negativamente en 31.19 y 21.17 por la biomasa y abundancia de las malezas respectivamente.

Producción de Paecilomyces fumosoroseus Brown & Smith y evaluación de su efectividad biólogica contra Bemisia argentifolii Bellows & Perring en cultivo de algodón Gossypium hirsutum L.

Tesis (Doctorado en Ciencias con especialidad en Biotecnología) U.A.N.L., Facultad de Ciencias Biol��gicas, 2007.

Influence of sodium chloride on seed germination and seedling root growth of cotton (Gossypium hirsutum L.)

Response of cotton (Gossypium hirsutum L. cv. NIAB-78) to salinity, in terms of seed germination, seedling root growth and root Na+ and K+ content was determined in a laboratory experiment. Cotton seeds were exposed to increasing salinity levels using germination water with Sodium chloride concentrations of 0, 50, 100, 150 and 200 mM, to provide different degrees of salt stress. Germinated seeds were counted and roots were harvested at 24, 48, 72 and 96 h after the start of the experiment. It appeared that seed germination was only slightly affected by an increase in salinity (in most cases the differences between treatment were non-significant), whereas root length, root growth rate, root fresh and dry weights were severely affected, generally highly significant differences in these variables were found for comparisons involving most combinations of salinity levels, in particular with increased incubation period. K+ contents decreased with increasing salinity levels, although differences in K+ content were only significant when comparing the control and the 4 salinity levels. Na+ content of the roots increased with increasing levels of NaCl in the germination water, suggesting an exchange of K+ for Na+. The ratio K+/Na+ strongly decreased with rising levels of salinity from around 4.5 for the control to similar to 1 at 200 mM NaCl.