Medida indireta da clorofila e sua relação com o manejo da adubação nitrogenada em plantas cítricas fertirrigadas

O planejamento da programação nutricional na citricultura requer a avaliação da disponibilidade de nutrientes através de análises de solo e folha, e também leva em consideração a expectativa de produtividade e a exportação de nutrientes pela colheita. A disponibilidade de nitrogênio (N) não tem sido eficientemente avaliada através de análises do solo e, em algumas áreas de cultivo de plantas cítricas, o N-foliar vem sendo empregado como guia para recomendação de N. O objetivo deste estudo foi avaliar a sensibilidade da medida indireta da clorofila como um método de monitoramento dos níveis de N em plantas cítricas. Para isso, um trabalho experimental de campo foi conduzido em Reginópolis-SP, durante dois anos, com as variedades de copa Valência e Hamlim, ambas sobre porta-enxerto citrumelo Swingle. Os tratamentos consistiram em cinco doses de N aplicadas via fertirrigação: 0; 35; 70; 140 e 280 kg ha-1 de N, na forma de nitrato de amônio. Todas as parcelas foram devidamente fertilizadas com fósforo, potássio e micronutrientes também através da fertirrigação. A medida indireta da clorofila foi avaliada pelo clorofilômetro, modelo SPAD-502, em folhas recém-maduras (3ª e 4ª folhas), nos quatro quadrantes, e na altura mediana da planta. As mesmas folhas foram utilizadas para a determinação do teor de N-foliar. As medidas de leitura SPAD e o teor de N na folha apresentaram respostas quadráticas às doses de N aplicadas. Correlação de 0,95 (p < 0,05) foi observada entre a medida indireta da clorofila e o teor de N foliar. Durante os estádios de desenvolvimento da cultura, os valores médios de leitura SPAD variaram em 11 unidades, e os teores médios de N foliar, em 5 unidades (g kg-1). Leituras SPAD abaixo de 70 e acima de 75 estiveram relacionadas, respectivamente, com plantas muito responsivas e não responsivas a N, enquanto plantas com leituras intermediárias devem ser adubadas com doses de N próximas daquelas extraídas com a colheita. Baseado em duas safras completas, conclui-se que a medida indireta da clorofila pode ser empregada como ferramenta rápida e não destrutiva no monitoramento e na avaliação da disponibilidade de N em plantas cítricas

Clorofila e carotenoides em maracujazeiro-amarelo irrigado com águas salinas no solo com biofertilizante bovino

Os efeitos deletérios provocados pelo estresse salino resultam em modificações nos mecanismos bioquímicos e fisiológicos das plantas, alterando, dentre outros, os teores foliares de clorofila e carotenoides, comprometendo a atividade fotossintética e, consequentemente, o crescimento, o desenvolvimento, a produção e a adaptabilidade aos ambientes adversos. O objetivo do trabalho foi avaliar os efeitos de diferentes condutividades elétricas da água de irrigação (CEai), associadas às épocas de aplicação de biofertilizante, sobre os teores de pigmentos fotossintéticos para a determinação dos pigmentos cloroplastídicos (clorofila a, b, total e carotenoides) do maracujazeiro-amarelo. Os tratamentos foram distribuídos em arranjo fatorial 5 x 4, referentes aos valores de CEai: 0,5; 1,5; 2,5; 3,5 e 4,5 dS m-1, em quatro épocas de aplicação do biofertilizante: sem biofertilizante (SB); aplicação uma semana antes do transplantio (1SAT); a cada 90 dias, a partir do transplantio (90DAT); uma semana antes e a cada 90 dias, após o transplantio (1SAT+90DAT). O aumento da concentração salina da água de irrigação reduziu a eficiência fotossintética nas folhas do maracujazeiro-amarelo, sendo mais drástico na condutividade superior a 2,5 dS m-1. As frequências de aplicação do biofertilizante não influenciaram nas concentrações dos pigmentos fotossintéticos.

Teor de clorofila e índice SPAD no abacaxizeiro cv. vitória em função da adubação nitrogenada

Tendo em vista a demanda do mercado por novas variedades e a necessidade de melhoria no manejo nutricional do abacaxizeiro, realizou-se este experimento com objetivo de avaliar o teor de clorofila e o índice SPAD no abacaxizeiro 'Vitória' em função da adubação nitrogenada com ureia e cama de frango. Para o efeito, foi instalado um experimento no delineamento em blocos casualizados, com quatro repetições. Os tratamentos consistiram em cinco doses de N, em duas fontes, orgânica (cama de frango) e mineral (ureia), totalizando nove combinações geradas através da matriz Composto Central de Box: T1, 44 e 2,91; T2, 152 e 0; T3, 0 e 10; T4, 44 e 17,1; T5, 260 e 2,91; T6, 152 e 10; T7, 152 e 20; T8, 304 e 10; e T9, 260 e 17,1 g planta-1. Foram avaliados o índice SPAD, o teor de clorofila na folha e o teor de N na folha D. Para o teor relativo de clorofila (SPAD), estimou-se o máximo valor com as doses de 16,37 g planta-1 de ureia e 200,69 g planta-1 de cama de frango. Para o teor de clorofila na folha D, obteve-se o valor máximo estimado com 19,4 g planta-1 de ureia. O índice SPAD possui correlação positiva com o teor de clorofila e com o teor de N na folha.

A técnica da reflectância difusa aplicada ao estudo da fluorescência de 2,3-naftalimidas n-substituídas com grupos alquila incluídas em b-ciclodextrina e adsorvidas em celulose microcristalina

The solution fluorescence of N-alkyl-2,3-naphthalimides (1-4) in polar protic and aprotic solvents was compared to the emission from solid samples resulting from the imide complexation with b-cyclodextrin or adsorption on the surface of microcrystalline cellulose. Solid samples of the inclusion complex 2,3-naphthalimides/b-cyclodextrin show maximum for fluorescence emission significantly different to the observed in methanolic solution. Beside this, a clear effect on the alkyl chain length could be observed for these samples which is probably due to differences in probe location inside the cyclodextrin cavity. The constancy for fluorescence quantum yield and fluorescence lifetime for the imides 1 - 4 adsorbed on microcrystalline cellulose suggests that, independently of the polarity of the solvent used for sample preparation, the probe is preferentially located on the cellulose surface. An increase of fluorescence quantum yield and fluorescence lifetime for solid samples, when compared to the values obtained in solution for the different solvents employed in this study (acetonitrile, methanol and water), is fully in accordance with a decrease of the probe mobility due to inclusion in b-cyclodextrin or to adsorption on cellulose.

Implementação de um sistema de eletroforese capilar com detecção de fluorescência induzida por laser

A capillary electrophoresis system using laser induced fluorescence detection is described. A Raman system equipped with a microscope has been used to focus the laser beam on the capillary giving a lateral resolution of 1.5 mm. The fluorescence signal of the analyte (ZnPcTS - tetrasulfonated zinc-phthalocyanine) was collected by the microscope objectives and analysed by a monochromator with confocal characteristics equipped with a CCD detector. Electropherograms obtained with this system were compared to those obtained on a commercial instrument, showing that the described system presents a lower detection limit and better resolution.

Métodos matemáticos para correção de interferências espectrais e efeitos interelementos na análise quantitativa por fluorescência de raios-X

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.

Extração por fluido supercrítico de alguns inseticidas carbamatos em amostras de batata, com determinação por HPLC/fluorescência e confirmação por HPLC/espectrometria de massas

Six supercritical fluid extraction (SFE) methods were tested, by varying the following operational parameters: CO2 pressure, time and temperature of extraction, type and proportion of static modifier, and Hydromatrix®/sample rate into cell. Firstly, insecticide carbamates were extracted from spiked potatoes samples (fortification level of 0,5 mg.Kg-1) by using SPE procedures, and then final extracts were analyzed HPLC/fluorescence. Good performance was observed with SFE methods that operated with values of temperature and CO2 pressure of 50 ºC and 350 bar, respectively. Best efficiency was obtained when it was used acetonitrile as a modifier (3% on the cell volume), and Hydromatrix®/sample rate of 2:1. Static time was of 1 min; total extraction time was of 35 min; dynamic extraction was performed with 15 mL of CO2, and it was used methanol (2 mL) for the dissolution of the final residue. In such conditions, pesticide recoveries varied from 72 to 94%, depending on the analyzed compound. In higher extraction temperatures, a rapid degradation was observed for some compounds, such as aldicarb and carbaryl; presence of their metabolites was further confirmed by HPLC-APCI/MS in positive mode. Detection limits for chromatographic analysis varied from 0,2 to 1,3 ng.

Aplicação de alguns modelos quimiométricos à espectroscopia de fluorescência de raios-X de energia dispersiva

The objective of this work was to accomplish the simultaneous determination of some chemical elements by Energy Dispersive X-ray Fluorescence (EDXRF) Spectroscopy through multivariate calibration in several sample types. The multivariate calibration models were: Back Propagation neural network, Levemberg-Marquardt neural network and Radial Basis Function neural network, fuzzy modeling and Partial Least Squares Regression. The samples were soil standards, plant standards, and mixtures of lead and sulfur salts diluted in silica. The smallest Root Mean Square errors (RMS) were obtained with Back Propagation neural networks, which solved main EDXRF problems in a better way.

Construção e avaliação de célula de fluxo para estudo da tensão interfacial dinâmica da interface fluxo líquido - sólido por despolarização da fluorescência

A simple low-cost flow cell was developed, built and optimized in order to observe dynamic interfacial tension of continuous flow systems. Distinct materials can be used in one of the cell walls in order to observe the intermolecular forces between the flowing liquid and the chemical constitution of the walls. The fluorescence depolarization was evaluated using Rhodamine B as fluorescent probe seeded in ethylene glycol. The effects of the positioning angles on the data acquired across the cell are reported. The reproducibility of the data was evaluated with a spectrometer assembled in-house and the relative standard deviation was below 3%.

Determinação de arsênio em águas contaminadas usando fluorescência de raios-X por energia dispersiva

This work proposes a simple, fast and inexpensive method to determine As in natural waters, using X-ray fluorescence. 50 µL of each sample containing 100 mg L-1 of yttrium as internal standard were deposited over a 2.5 µm thickness MylarTM film. The samples were dried at 50 °C for 2 h. X-ray spectra were obtained using an EDXRF apparatus. The accuracy was determined by analyte addition/recovery and by comparison with Hydride Generation Atomic Absorption Spectrometry (HG AAS). A recovery of about 100% was obtained and the results were in good agreement with HG AAS. The method showed a relative standard deviation of 6.8% and a detection limit of 10.5 µg L-1 of As.

Um novo método para quantificar mercúrio orgânico (Hg orgânico) empregando a espectrometria de fluorescência atômica do vapor frio

In this work a simple and sensitive procedure to extract organic mercury from water and sediment samples, using methylene chloride in acidic media followed by CVAFS quantification has been developed. The method was evaluated for possible interferents, using different inorganic mercury species and humic acid, no effects being observed. The detection limit for organic mercury was 160 pg and 396 pg for water and sediment samples respectively. The accuracy of the method was evaluated using a certified reference material of methylmercury (BCR-580, estuarine sediment). Recovery tests using methylmercury as surrogate spiked with 1.0 up to 30.0 ng L-1 ranged from 90 up to 109% for water samples, whereas for sediments, recoveries ranged from 57 up to 97%.

Desenvolvimento e validação de um método analítico para a determinação de histamina em vinhos utilizando cromatografia líquida de alta eficiência com detecção por fluorescência

A rapid and efficient method for the analysis of histamine in wines using HPLC with fluorescence detection after derivatization was developed and validated. The method LOD and LOQ values were 0.25 and 0.50 mg L-1 respectively. The repeatability and intermediary precision for the instrument and for the method presented RSD values of 3.7 and 2.9%, and 6.0 and 5.6%, respectively. The recoveries were 95.5 and 89.9% for the fortification levels of 2 and 10 mg L-1. The method was applied to determine the histamine content in Cabernet Sauvignon wines, which presented values between 1.2 and 5.7 mg L-1.

Análise arqueométrica de cerâmica Tupiguarani da região central do Estado do Rio Grande do Sul, Brasil, usando fluorescência de raios X por dispersão de energia (EDXRF)

Energy dispersive X-ray fluorescence methodology (EDXRF) was used to determine Al, Ba, Ca, Cr, Fe, K, Mn, Pb, Rb, S, Si, Sr, Ti, V, Zn in pottery sherds from seven archaeological sites in the central region of Rio Grande do Sul State, Brazil. The potteries' chemical fingerprints from Ijuí River, Ibicuí Mirim River, Vacacaí Mirim River and Jacuí River were identified. Interactions between sites from the Jacuí River, Vacacaí Mirim River and Ibicui Mirim River could have occurred because some samples from these sites are overlapping in a principal component analysis (PCA) graphic. The pottery provenance could be the same.

Análise de fluorescência de substâncias húmicas extraídas da água, solo e sedimento da Lagoa dos Patos - MS

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.

Determinação de 3,4-metilenodioximetanfetamina (MDMA) em comprimidos de Ecstasy por cromatografia líquida de alta eficiência com detecção por fluorescência (CLAE-DF)

This paper describes the development and validation of simple and selective analytical method for determination of 3.4-methylenedioxymethamphetamine (MDMA) in Ecstasy tablets, using high performance liquid chromatography with fluorescence detection. Analysis was performed in a reversed phase column (LiChrospher 100 C18, 150 x 4.6 mm, 5 µm), isocratic elution with phosphate buffer 25 mmol/L pH 3.0 and acetonitrile (95:5, v/v). The method presents adequate linearity, selectivity, precision and accuracy. MDMA concentration in analyzed tablets showed a remarkable variability (from 8.5 to 59.5 mg/tablet) although the tablet weights were uniform, indicating poor manufacturing control thus imposing additional health risks to the users.