769 resultados para potato apyrase


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Iniciou-se em 1986, em Anápolis, um programa de desenvolvimento de cultivares de batata adaptadas ao clima de altitude do Brasil Central, partindo-se de 15.000 genótipos, resultantes de 200 famílias obtidas pela Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA) Hortaliças em 1985 e 1986. No primeiro ciclo, em 1986, foram selecionados 5.000 genótipos, considerando-se aspectos fenológicos, incidência de doenças, qualidade dos tubérculos e potencial de produção. Esses mesmos critérios foram adotados nas gerações posteriores, selecionando-se, anualmente, 15-20% de genótipos superiores. em 1990 avaliaram-se 52 destes clones, tendo como testemunhas as cultivares Achat e Bintje; Destes foram selecionados 28 clones promissores que foram submetidos à cultura de ápices caulinares e à indexação para os vírus PLRV, PVY e PVX na Empresa Brasileira de Pesquisa Agropecuária (EMBRAPA) Hortaliças. No período de 1995 a 1997 foram avaliados em Goiás, nos municípios de Anápolis, Morrinhos, Pirenópolis e Urutaí, e em Jaboticabal. Os dados foram submetidos à análise de variância, e aqueles referentes a 14 genótipos em 7 ambientes, à regressão pelo método de Eberhart & Russell. Os clones BAT 2, BAT 3, BAT 4, BAT 19, BAT 27 e BAT 28 destacaram-se entre os mais produtivos, considerando-se, também, as características de tubérculos para o consumo. Os genótipos responderam proporcionalmente à melhoria do ambiente. O clone BAT 19 foi o mais estável.

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Estudou-se o efeito de concentrações de bissulfureto de carbono sobre a brotação de mini-tubérculos de batata. O ensaio foi instalado no esquema fatorial 5 x 7, onde as variáveis constaram de quatro diferentes doses de bissulfureto de carbono (10; 20; 30 e 40 mg L-1) além do controle e sete cultivares de batata (Bintje, Jaete Bintje, Atlantic, Cupido, Ágata, Monalisa e Mondial). Os tratamentos com bissulfureto de carbono foram aplicados durante um período de 72 horas, após o qual os mini-tubérculos de batata foram colocados em bandejas de isopor para brotação. de forma geral, todas as concentrações de bissulfureto de carbono estimularam a brotação. As cultivares Bintje e Atlantic responderam de forma positiva ao bissulfureto de carbono, onde o aumento da concentração levou ao aumento do número de brotos por tubérculo. As cultivares Ágata e Mondial responderam positivamente à concentração de 10 mg L-1, sendo que o acréscimo nas concentrações pouco interferiu no número de brotos por tubérculo. As cultivares Jaete Bintje e Monalisa só responderam às concentrações de 20 e 30 mg L-1, e na de 40 mg L-1 o bissulfureto de carbono provocou a queima de gemas.

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Avaliou-se a resistência (e antibiose) de genótipos de batata, comerciais e em fase de melhoramento, ao pulgão Myzus persicae, em ensaios efetuados com plantas em vasos, sem chance de escolha, em Jaboticabal (SP). Foram efetuados seis experimentos, utilizando-se um total de 16 genótipos, a saber: 'Achat', 'Apuã', 'Aracy', 'Aracy Ruiva', 'Bintje', 'Ibitu Açu', 'Itararé', 'N 140-201', 'NYL 235-4', '288.719-13', '288.764-26', '288.776-3', '288.776-6', '288.794-19', '288.801-6' e '288.814-7'. em cada experimento foram utilizadas combinações variadas dos mesmos. Nos dois primeiros experimentos as plantas foram infestadas com 30 pulgões adultos por planta, distribuídos em três folhas, com três avaliações realizadas em semanas subseqüentes à infestação, contando-se o número de indivíduos por planta. O terceiro experimento foi conduzido aprisionando-se duas fêmeas adultas no interior de pequenas gaiolas fixadas na face abaxial dos folíolos, em número de dez por planta, avaliando-se a reprodução do pulgão após sete dias, em dois plantios. No quarto experimento efetuou-se a infestação da planta com 15 pulgões, avaliando-se o crescimento da população na planta toda durante três semanas consecutivas. No quinto experimento foi avaliada a descendência de uma única fêmea adulta por folíolo e no sexto experimento avaliou-se o peso dos pulgões aos sete dias de vida. Os tricomas glandulares presentes nos folíolos e a funcionalidade dos mesmos também foram avaliados. A cultivar 'Ibitu Açu' apresentou elevado grau de antibiose a M. persicae; os genótipos '288.776-3' e '288.794-19' também apresentaram esse tipo de resistência, em grau moderado; '288.719-13' e '288.764-26' foram resistentes ao pulgão, provavelmente devido à presença de tricomas glandulares funcionais, dos tipos A e B, em seus folíolos (antixenose); entre os mais suscetíveis destacaram-se 'Bintje' e '288.801-6'.

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

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O presente trabalho objetivou investigar se meios de cultura utilizados em teste de viabilidade afetam a germinação de conídios de cinco isolados de Lecanicillium lecanii, cinco de Beauveria bassiana e quatro de Paecilomyces fumosoroseus. Os testes foram realizados em lâminas de microscopia contendo um dos seguintes meios de cultura: Ágar-água (AA), Meio Mínimo (MM), Batata, dextrose e ágar (BDA), Batata, dextrose, ágar e 1% de extrato de levedura (BDAL), Sabouraud, dextrose, ágar e extrato de levedura (SDAL) e Meio Completo (MC). Delimitaram-se três áreas por lâmina e em cada uma aplicou-se 0,05mL de uma suspensão com concentração de 5,5 x 105 conídios ml-1. Para cada isolado foi realizado um bioensaio, com seis tratamentos e cinco repetições. Avaliou-se a germinação 15 horas após incubação, a 26±0,5ºC. Os meios de cultura influíram na capacidade de germinação das três espécies estudadas, ocorrendo variações inter e intraespecíficas. Verificou-se que os meios Completo e BDA proporcionaram as maiores porcentagens de germinação dos isolados de L. lecanii, sendo que e as menores foram obtidas nos meios SDAL e AA. Os meios ricos em nutrientes (BDA, BDAL e Completo) favoreceram a germinação dos isolados de B. bassiana, o que não ocorreu com os meios pobres (AA e MM). Nos meios Completo e BDA foram obtidas as maiores porcentagens de germinação dos isolados de P. fumosoroseus. As menores percentagens, por sua vez, foram obtidas no meio SDAL. Entretanto, alguns isolados apresentaram alta germinação em meios pobres em nutrientes (AA e MM).

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Inúmeros trabalhos têm demonstrado o efeito benéfico da adubação com silício sobre o acréscimo da produção de diversas culturas, como, por exemplo, arroz, cana-de-açúcar e batata. No entanto, são escassas as informações sobre os benefícios nutricionais do silício para a cultura do milho. Desta maneira, objetivou-se, neste estudo, avaliar o efeito de doses e épocas de aplicação de silício, via foliar, nas características agronômicas e na produtividade do milho, cultivado no ano agrícola 2007/2008. O delineamento experimental adotado foi o de blocos casualizados, em esquema fatorial (4 x 3) + 1, com quatro repetições, envolvendo doses de silício (130, 260, 390 e 520 g ha-1 de Si) aplicadas via foliar, épocas de aplicação (2, 5 e 8 folhas expandidas) e uma testemunha (sem aplicação de Si). As variáveis analisadas foram altura das plantas e a inserção da primeira espiga, diâmetro de colmo, índice de clorofila foliar, teor foliar de silício, número de grãos por espiga, massa de 100 grãos e produtividade de grãos. O silício aplicado via foliar influenciou somente o teor foliar de Si.

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

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Brazilian isolates of Colletotrichum spp. from citrus orchards affected by postbloom fruit drop were examined for colony colour, mycelial growth, benomyl-resistance, pathogenicity, and genetic variability by random amplified polymorphic DNA (RAPD) analysis. All isolates were obtained from flowers and persistent calyxes from different citrus hosts from São Paulo, Brazil. DNA polymorphisms detected after amplification with random 10-mer primers were used to classify the isolates into two groups. Group I isolates grew rapidly on potato-dextrose agar (PDA) and were sensitive to benomyl, and group II isolates grew slowly on PDA and were benomyl-resistant. Colletotrichum acutatum was analyzed by RAPD and had high genetic similarity with group II isolates of Colletotrichum from citrus. Probably, the group I is C, gloeosporioides and group II is C. acutatum.

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Twelve isolates of Paracoccidioides brasiliensis generated cerebriform colonies at room temperature on potato glucose agar slants (PDA). These isolates contained abundant chlamydospores and yeast-like cells and are a subset of the 65 isolates obtained from nine-banded armadillos (Dasypus novemcinctus). They grew as a yeast form with typical multiple buddings at 37 degreesC on brain heart infusion agar supplemented with 1% glucose. After replating on PDA and culturing at room temperature for 2 months, the mutants appeared as cottonous colonies, which indicated that the morphological characteristics were unstable.

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Colletotrichum spp. cause anthracnose in various fruits post-harvest and are a particularly important problem in tropical and subtropical fruits. The disease in fruits of avocado, guava, papaya, mango and passion fruit has been reported to be caused by C. gloeosporioides, and in banana by C. musae. In subtropical and temperate crops such apple, grape, peach and kiwi, the disease is caused by C. acutatum. The variation in pathogenic, morphological, cultural and molecular characteristics of Brazilian isolates of Colletotrichum acutatum Simmonds and isolates from post-harvest decays of avocado, banana, guava, papaya, mango and passion fruit was evaluated. The fruits were inoculated with mycelium of C. acutatum, Colletotrichum spp. and C. musae on a disc of potato dextrose agar. The morphological, cultural and molecular characteristics studied were conidia morphology, colony growth at different temperatures, colony coloration and PCR with primers CaInt2 and ITS4 for C. acutatum and CgInt and ITS4 for C. gloeosporioides. C. acutatum was pathogenic to avocado, guava, papaya, mango and passion fruit, but it was not pathogenic to banana. The morphological, cultural and molecular studies indicated that the avocado, papaya, mango and passion fruit isolates were C. gloeosporioides. The natural guava isolate was identified as C. acutatum, which had not been found previously to produce anthracnose symptoms on guava in Brazil.

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Several statistical models can be used for assessing genotype X environment interaction (GEI) and studying genotypic stability. The objectives of this research were to show how (i) to use Bayesian methodology for computing Shukla's phenotypic stability variance and (ii) to incorporate prior information on the parameters for better estimation. Potato [Solanum tuberosum subsp. andigenum (Juz. & Bukasov) Hawkes], wheat (Triticum aestivum L.), and maize (Zea mays L.) multi environment trials (MET) were used for illustrating the application of the Bayes paradigm. The potato trial included 15 genotypes, but prior information for just three genotypes was used. The wheat trial used prior information on all 10 genotypes included in the trial, whereas for the maize trial, noninformative priors for the nine genotypes was used. Concerning the posterior distribution of the genotypic means, the maize MET with 20 sites gave less disperse posterior distributions of the genotypic means than did the posterior distribution of the genotypic means of the other METs, which included fewer environments. The Bayesian approach allows use of other statistical strategies such as the normal truncated distribution (used in this study). When analyzing grain yield, a lower bound of zero and an upper bound set by the researcher's experience can be used. The Bayesian paradigm offers plant breeders the possibility of computing the probability of a genotype being the best performer. The results of this study show that although some genotypes may have a very low probability of being the best in all sites, they have a relatively good chance of being among the five highest yielding genotypes.

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Several clean-up procedures which included the use of glass chromatography columns (silica gel, alumina, Florisil, silanized Celite-charcoal), Sep-Pak cartridges and standard solutions were compared for the determination of the following N-methylcarbamate (NMC) insecticides: aldicarb, carbaryl, carbofuran, methomyl and propoxur. According to recovery results of the compounds after elution in a glass column, the most efficient systems employed 4.6% deactivated alumina and a silanized Celite-charcoal (4:1) as adsorbents, using dichloromethane-methanol (99:1) and toluene-acetonitrile (75:25) mixtures, respectively, as binary eluents. The recoveries of the compounds studied varied from 84 to 120%. Comparable recoveries (75-100%) for Sep-Pak cartridges in normal phase (NH2, CN) and reversed phase (C-8) were observed. Different temperatures were tested during the concentration step in a rotary evaporator, and we verified a strong influence of this parameter on the stability of some compounds, such as carbofuran and carbaryl. Recovery studies employing the best clean up procedures were performed at the Brazilian agricultural level in potato and carrot samples; Validation methodology of the US Food and Drug Administration was adapted for the N-methylcarbamate analysis. Their recoveries ranged between 79 and 93% with coefficients of variation of 2.3-8%. (C) 1998 Elsevier B.V. B.V.

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Background: the soil fungus Rhizoctonia solani anastomosis group 3 (AG-3) is an important pathogen of cultivated plants in the family Solanaceae. Isolates of R. solani AG-3 are taxonomically related based on the composition of cellular fatty acids, phylogenetic analysis of nuclear ribosomal DNA (rDNA) and beta-tubulin gene sequences, and somatic hyphal interactions. Despite the close genetic relationship among isolates of R. solani AG-3, field populations from potato and tobacco exhibit comparative differences in their disease biology, dispersal ecology, host specialization, genetic diversity and population structure. However, little information is available on how field populations of R. solani AG-3 on potato and tobacco are shaped by population genetic processes. In this study, two field populations of R. solani AG-3 from potato in North Carolina (NC) and the Northern USA; and two field populations from tobacco in NC and Southern Brazil were examined using sequence analysis of two cloned regions of nuclear DNA (pP42F and pP89).Results: Populations of R. solani AG-3 from potato were genetically diverse with a high frequency of heterozygosity, while limited or no genetic diversity was observed within the highly homozygous tobacco populations from NC and Brazil. Except for one isolate (TBR24), all NC and Brazilian isolates from tobacco shared the same alleles. No alleles were shared between potato and tobacco populations of R. solani AG-3, indicating no gene flow between them. To infer historical events that influenced current geographical patterns observed for populations of R. solani AG-3 from potato, we performed an analysis of molecular variance (AMOVA) and a nested clade analysis (NCA). Population differentiation was detected for locus pP89 (Phi(ST) = 0.257, significant at P < 0.05) but not for locus pP42F (Phi(ST) = 0.034, not significant). Results based on NCA of the pP89 locus suggest that historical restricted gene flow is a plausible explanation for the geographical association of clades. Coalescent-based simulations of genealogical relationships between populations of R. solani AG-3 from potato and tobacco were used to estimate the amount and directionality of historical migration patterns in time, and the ages of mutations of populations. Low rates of historical movement of genes were observed between the potato and tobacco populations of R. solani AG-3.Conclusion: the two sisters populations of the basidiomycete fungus R. solani AG-3 from potato and tobacco represent two genetically distinct and historically divergent lineages that have probably evolved within the range of their particular related Solanaceae hosts as sympatric species.

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A competitive enzyme-linked immunosorbent assay (ELISA) method for carbaryl quantitation in crop extracts was validated by liquid chromatography (LC) with diode array detection (DAD). For this purpose, six crops (banana, carrot, green bean, orange, peach and potato) were chosen for recovery and reproducibility studies. The general sample preparation included extraction with methanol followed by liquid-liquid partitioning and clean-up on Celite-charcoal adsorbent column of the vegetable extracts. ELISA samples consisted of a diluted LC extract in assay phosphate buffer (pH 7.5). The potential effect of methanol in these samples was evaluated. It was observed that a maximum content of 10% methanol present in the assay buffer could be tolerated without expressive losses in the ELISA performance. Under these conditions, a IC50 similar to 1.48 mu g l(-1) was obtained. A minimum matrix effect with a 1:50 dilution of the methanolic extracts in assay buffer was noticed, except for green bean samples that inhibited completely the assay. For the vegetable extracts, the ELISA sensitivities varied from 3.9 to 5.7 mu g l(-1), and good recoveries (82-96%) with R.S.D.s ranging from 5.7 to 12.1% were found. An excellent correlation between the LC-DAD and ELISA techniques was obtained. The confirmation of the carbaryl in less concentrated samples was achieved by LC-mass spectrometry interfaced with atmospheric pressure chemical ionisation. The [M + H](+)= 202 and [M + H-57](+)=145 ions, equivalent to the protonated molecular and l-naphthol ions, respectively, were used to carbaryl identification in these samples. (C) 1998 Elsevier B.V. B.V. All rights reserved.

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Starches from six different species (cassava, arrowroot, sweet potato, yam, canna and ginger) were isolated and some structural and physicochemical characteristics analysed and correlated. Phosphorous and amylose contents were determined using a colorimetric method and measuring iodine affinity, respectively. Molecular weight distributions of starches were analysed by Sepharose CL 2B. Granular shape and size distribution were performed using an image analyser system attached to a light microscope. Swelling power was determined at 60, 70, 80 and 90 degrees C. Pasting and thermal properties were measured using a rapid viscoanalyser, and a differential scanning calorimeter, respectively. Phosphorous content varied from 0.007 to 0.031% for cassava and canna starches, respectively. Yam, canna and ginger starches displayed higher amylose contents (32.6, 31.7 and 26.5%, respectively) than cassava, arrowroot and sweet potato starches (19.8, 20.8 and 22.6%, respectively). These last three starches displayed amylose molecules of higher molecular weight than those shown for yam, canna and ginger starches. Canna starch showed higher proportions of longer branch chains of amylopectin than others starches. The size and shape of granules were quite variable among all starches and the average size of granules varied from 13.9 to 42.3 mu m for sweet potato and canna, respectively. Swelling power, pasting, and thermal properties were affected by structural characteristics of the starches.