996 resultados para métodos de análise de solo


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O objetivo deste trabalho foi avaliar possíveis alterações na densidade e na porosidade total do solo, em razão do pisoteio de cordeiros, sob diferentes manejos, após as culturas de verão em plantio direto. O experimento foi realizado em Argissolo Vermelho distrófico argiloso, nas camadas 0-2,5, 2,5-5 e 5-10 cm, em pastagem de azevém anual manejada com ofertas de forragem de 2,5 ou 5,0 vezes o potencial de consumo dos animais, em lotação contínua e rotacionada. Como testemunha, utilizou-se uma área não pastejada. As intensidades de pastejo e os métodos de pastoreio não tiveram efeito sobre a densidade e a porosidade total do solo. É possível utilizar, durante o inverno, áreas com este tipo de textura do solo, com culturas de cobertura para pastejo de cordeiros, sem que as alterações nos atributos físicos do solo, pelo pisoteio animal, atinjam níveis prejudiciais para as culturas subsequentes.

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O objetivo deste trabalho foi avaliar, por meio da análise dos componentes principais, a redução na dimensionalidade de atributos químicos e físicos do solo para a compreensão da variabilidade espacial e temporal da produtividade de culturas de grãos. A área experimental, de 54 ha, é manejada em agricultura de precisão há oito anos. Com base em seis mapas de colheita (soja - safra 2000/2001; milho - 2001/2002; soja - 2002/2003; trigo - 2003; soja - 2003/2004; e milho - 2004/2005), a área foi dividida em três zonas de produtividade de grãos (alta, média e baixa). Foram definidos 15 pontos georreferenciados representativos, para determinação de atributos químicos e físicos do solo, o que totalizou 63 variáveis analisadas. Entre os atributos químicos, o elevado teor de K no solo é o que melhor explica a variabilidade espacial da produtividade das culturas de grãos, provavelmente em razão do desbalanço das relações Ca:K e Mg:K. A zona de baixa produtividade apresentou baixa qualidade física do solo. Neste caso, a infiltração de água no solo, isoladamente, é a variável que melhor explica o desempenho das culturas de grãos. A análise dos componentes principais dos atributos químicos e físicos do solo é estratégia eficiente para explicar a variabilidade espacial e temporal da produtividade de culturas de grãos.

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O objetivo deste trabalho foi avaliar a perda de solo de área de nascentes da Microbacia do Córrego do Tijuco, SP. Foi utilizada a análise espacial dos fatores da equação universal da perda de solo (EUPS), em integração com análise de componentes principais e geoestatística. A perda de solo média, estimada para a área, foi de 118,5 Mg ha‑1 por ano, considerada alta. Próximo à zona urbana, houve alta interação dos fatores erosividade da chuva e práticas conservacionistas, o que evidencia grande perda de solo, em razão da concentração da água proveniente da camada impermeabilizada urbana, com alta velocidade de escoamento. Nos divisores de águas, a atuação da erodibilidade foi proeminente, em contraste com o fator topográfico. Foram observadas áreas com atuação conjunta destes fatores, inclusive em locais de inclinação suave, porém com alto potencial natural de erosão. A interação das análises multivariadas e geoestatística permite a estratificação da área, identifica locais com propriedades específicas quanto à perda de solo, e espacializa os fatores do processo erosivo e suas interações ao longo do relevo.

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The FTIR spectroscopy has been used to quantify the secondary structures of proteins, using amide I band (1600 - 1700 cm-1). The resolution enhancement methods have been used to resolve the individual components of this band that correlate to the secondary structure. In this paper we discuss the methods of derivative, Fourier deconvolution and fitting with simulated spectra. The results shows that they have serious problems and can be used only as a qualitative or semiquatitative method.

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One of the major interests in soil analysis is the evaluation of its chemical, physical and biological parameters, which are indicators of soil quality (the most important is the organic matter). Besides there is a great interest in the study of humic substances and on the assessment of pollutants, such as pesticides and heavy metals, in soils. Chemometrics is a powerful tool to deal with these problems and can help soil researchers to extract much more information from their data. In spite of this, the presence of these kinds of strategies in the literature has obtained projection only recently. The utilization of chemometric methods in soil analysis is evaluated in this article. The applications will be divided in four parts (with emphasis in the first two): (i) descriptive and exploratory methods based on Principal Component Analysis (PCA); (ii) multivariate calibration methods (MLR, PCR and PLS); (iii) methods such as Evolving Factor Analysis and SIMPLISMA; and (iv) artificial intelligence methods, such as Artificial Neural Networks.

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The objective of this study was to evaluate a flow injection system for determination of residual CO3(2-) in soil amended with lime material. It was used a closed system were the CO2 released from soil sample acidified with 0.5 mol L-1 HCl was capted in a 0.2 mol L-1 NaOH solution. After 16h the capted CO2 was determined by conductivimetry using a flow injection system. The results obtained by the proposed method were significantly correlated with those reported in soil samples used by the International Soil Analytical Exchange Programe. The regression equation was: y = 0.987x -- 0.075 r = 0.996, P > 0.01. For acid soils amended with CaCO3 the method showed a deviation error of 2.7%, detection limit was 0.077 mmol kg-1 of CO3(2-), and a recovery of 99.7% of the total CO3(2-) added in soil sample. The method was easily adapted for routine determination of residual CO3(2-) in soil samples with an analytical frequency of 40 samples per hour.

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One of the main problems in quantitative analysis of complex samples by x-ray fluorescence is related to interelemental (or matrix) effects. These effects appear as a result of interactions among sample elements, affecting the x-ray emission intensity in a non-linear manner. Basically, two main effects occur; intensity absorption and enhancement. The combination of these effects can lead to serious problems. Many studies have been carried out proposing mathematical methods to correct for these effects. Basic concepts and the main correction methods are discussed here.

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Relevant aspects of proposed mechanisms of the chemiluminescent reaction of luminol are presented and commented to emphasize its perspectives for kinetic analysis. A careful search for analytical applications of this reaction is discussed in order to point out new trends of the studies. Kinetic analysis using the luminol reaction is proposed to be a very attractive due to the good performance of the reaction in analytical applications and the positive characteristics of kinetic analysis, such as low cost and sensibility. It is pointed out that kinetic analysis using the chemiluminescent reaction of luminol should be encouraged.

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In the present work, we analyzed the accuracy of distinct theoretical methods to reproduce the solid state structures of cyclodextrins. The a, b and g-cyclodextrins (CD) were considered and also their hydrates with included water molecules: a-CD.2H2O, b-CD.10H2O and g-CD.12H2O. The geometries were fully optimized using Molecular Mechanics (MM2), semiempirical (AM1 and PM3) and ab initio (HF/3-21G) methods and quantitatively compared with experimental data from X ray diffraction. The results obtained from the classical MM2 method were in best agreement with the experiment. The semiempirical and ab initio structures were also in satisfactory accordance with the experimental data. In general, the PM3 method was found to be more suitable than the AM1 to describe the CD geometries, mainly when the intramolecular hydrogen bonds are considered.

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Immunoassay techniques provide simple, powerful and inexpensive methods for analysis of environmental contaminants. However, the acceptance of immunoassays is dependent on the clear demonstration of quality and validity compared to more traditional techniques. In this review, primarily, the understanding and the fundamentals of immunoassay methods are given in order to make good use of immunoassays, especially of EIA tests. Special attention is given to the concepts related to the enzyme-linked immunosorbent assay (ELISA) formats, such as inhibition concentration at 50% (IC50), detection limit (LOD), cross-reactivity (CR %). It is also explained why some immunoassays are quantitative methods whereas others can only be used as screening methods. A list of main commercial kits for detection of priority pollutants is given in order to help analysts. Others formats, such as flow-injection immunoassay analysis (FIIA), immunoassay chromatography and immunosensors are also cited.

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Analysis of diazepam (DZP) and its active metabolite nordiazepam (NDZP) in plasma is commonly performed in clinical medicine to ensure proper therapeutic effects while minimizing the incidence of toxicity. This study aimed to optimize analytical parameters and compare two pre-treatment techniques, liquid-liquid (LLE) and solid phase extraction (SPE), as well as liquid chromatographic conditions to analyze simultaneously DZP and NDZP in plasma from 20 patients treated with a daily dose of 10 mg. Both techniques showed to be well in line with the international criteria for analytical validation, which permitted to quantify DZP (66.2 - 1148.6 ng mL-1) and NDZP (138.5 - 808.6 ng mL -1) in all samples. The correlation coefficients between SPE and LLE were respectively 0.9729 for DZP and 0.9643 for NDZP.

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Complex B vitamins are present in some cereal foods and the ingestion of enriched products contributes to the recommended dietary intake of these micronutrients. To adapt the label of some products, it is necessary to develop and validate the analytical methods. These methods must be reliable and with enough sensitivity to analyze complex B vitamins naturally present in food at low concentration. The purpose of this work is to evaluate, with validated methods, the content of vitamins B1, B2, B6 and niacin in five cereal flours used in food industry (oat, rice, barley, corn and wheat).

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This work presents a review of sampling and analytical methods that can be applied to atmospheric traces of reduced sulphur compounds (RSC) in the atmosphere. Sampling methodology involving discontinuous methods with preconcentration is mostly used. For the most part, adsorption on solids and cryogenic capture are applied as a procedure. The analysis of these compounds has been done mainly by gas chromatography with FPD, fluorescence and spectrophotometry. Advantages and disadvantages of the methodologies are also mentioned in this paper, aiming to guide the reader towards the most appropriate choice of a sampling and analytical method for RSCs.

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The humic substances were extracted from sediments, water and soil close to the Lagoa dos Patos-MS. The characterization was performed through fluorescence emission. In the HSs it is possible to see strong indications of incorporation of compounds originating from lignin degradation, confirmed by fluorescence emission (EEM and synchronous spectra). These differences observed in HSs may be due to tropical regions displaying a great variety of vascular plants and aquatic macrophytes that contribute natural organic matter. The seasonality effect also causes the entrance of pedogenic material and the suspension of sediments by the action of winds.

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The validation of analytical methods is an important step in quality control. The main objective of this study is to propose an HPLC experiment to verify the parameters of validation of chromatographic methods, based on green chemistry principles, which can be used in experimental courses of chemistry and related areas.