A aplicação de ar quente em videiras foi primeiramente realizada na fazenda do Sr. Florenzo Lazo, localizada no Chile, onde havia a necessidade de combater os efeitos negativos das freqüentes geadas que resultava em severos danos à lavoura. Por este motivo o Sr. Florenzo inventou uma máquina que aplicava ar quente com baixa umidade e tinha por objetivo dispersar o ar frio proveniente das geadas. Após certo tempo, foi observado pelo produtor que no local onde a máquina havia operado com maior frequência as plantas apresentavam-se com uma coloração mais escura e com sinais de maior vitalidade. Seguindo estas observações, relacionamos estes efeitos a um possível aumento nos fito-hormônios relacionados ao estresse vegetal e à SAR (Systemic Resistence Adquired), como o ácido salicílico (AS), ácido jasmônico (AJ) e ácido abscísico (ABA), além de fazer uma correlação com alguns resultados de pós-colheita importantes para a comercialização, como: Sólidos solúveis, firmeza e coloração. Para isso foi montado um experimento que foi conduzido em duas parcelas, sendo uma com tratamento TPC e outra apenas com o tratamento convencional com distância padronizada em 3,2 metros entre linhas por 2,0 metros entre planta. As amostras eram coletadas diariamente e devidamente acondicionadas. Ao final da safra, as amostras foram transportadas para o laboratório de estresse e neurofisiologia da universidade de São Paulo (LEPSE), onde foram novamente armazenadas em um Ultra-freezer - 86ºC. As analises fisiológicas de pós-colheita foram realizadas no departamento de pós-colheita da universidade de São Paulo onde foram analisados os teores de sólidos solúveis, coloração e firmeza das bagas de uva. As amostras de folhas foram maceradas e uniformizadas no LEPSE e enviadas para o laboratório de ecotoxicologia do Centro de Energia Nuclear na Agricultura (CENA) onde foram mensurados os teores dos fito-hormônios pelo método de espectrometria de massa. Para ambas as analises foram feitos testes estatísticos utilizando o programa SAS®. Não houve alteração de SS e firmeza entre os dois tratamentos para as características fisiológicas de póscolheita. Entretanto foi notado uma redução na coloração avermelhada para os cachos tratados com TPC seguindo o sistema de colorimetria proposto pelo CIE. Não houve alterações significantes para as variáveis ABA, AJ e AS para o efeito tratamento e para a analise de correlação. Entretanto notou-se significância entre o efeito dias para as variáveis ABA e AJ. Não foi notada significância para o efeito dias para a variável AS. Por se tratar de um estresse rápido, a TPC parece não causar estresse imediato nas plantas, entretanto notou-se indução de estresse ao longo do tempo, possivelmente devido à resposta lenta de ABA que aparentemente está envolvida com RNA e à síntese de proteínas S e R- ABA que são igualmente efetivas. Já para o AJ sugere-se que houve a produção de H2O2 por derivados de oligogalacturonideos, liberados por ação da enzima poligalacturonase, e um segundo mensageiro que ativam genes defensivos (genes tardios). O aumento na biossíntese do ABA e do AJ parece ter suprimido genes envolvidos na biossíntese do AS. / The application of hot air in grapevines was first held on the farm of Mr. Florenzo Lazo, located in Chile, to combat the negative effects of frequent frosts that resulted in severe damage to the crop. For this reason Mr. Florenzo invented a machine that applied hot air with low humidity and aimed to disperse the cold air from the frost. After a while, it was observed by the producer that where the machine had operated more frequently plants showed up with a darker and more signs of vitality. Following these observations, these effects relate to a possible increase in phytohormones related to plant stress and SAR (Systemic Resistance Adquired), such as salicylic acid (AS), jasmonic acid (AJ) and abscisic acid (ABA), besides making a correlation with results of some important postharvest for marketing, such as soluble solids, firmness and color. For this experiment was created that was conducted in two installments, the first one was treated with TPC and second one was applied only conventional treatment with standardized distance of 3.2 meters between lines by 2.0 meters between plant . The samples were collected daily and properly packed. At the end of the season, samples were transported to the laboratory stress and neurophysiology from the University of São Paulo (LEPSE), where they were again stored in an Ultra-freezer - 86 degrees. The physiological analyses of post-harvest were performed at the Department of Postharvest in University of Sao Paulo where we analyzed the levels of soluble solids, firmness and color in grape berries. The leaf samples were uniform macerated at LEPSE and sent to the laboratory of ecotoxicology in the Center for Nuclear Energy in Agriculture (CENA) where we measured the levels of the phytohormones by the method of mass spectrometry. For both analyzes were performed statistical tests using SAS ® program. There wasn`t change between the two treatments on physiological post-harvest characteristics. There was no change of SS and firmly between the two treatments for the physiological of post-harvest characteristics. However it was noted a reduction in red color for bunches treated with TPC following the colorimetry system by CIE. There were no significant changes to the variables ABA, AJ and AS for the treatment effect and to analyze the correlation. However significance was noted between the effect variables ABA days and AJ. No significant effect was noted for days variable for AS. Since it is a stress fast TPC does not seem to cause immediate stress in plants but it was noticed induction of stress over time, possibly due to slow response to ABA which apparently is involved in the synthesis of RNA and proteins S and R-ABA that are equally effective. As for AJ suggests that there was the production of H2O2 by derivatives of oligogalacturonides, released by action of the enzyme polygalacturonase, and a second messenger that activates defensive genes (late genes). The increase in ABA biosynthesis and AJ appears to have deleted genes involved in the biosynthesis of AS.

Atmospheric aerosols have adverse effects on human health, air quality, and visibility and frequently result in severe pollution events, particularly in urban areas. However, the sources of aerosols and the processes governing their behaviour in the atmosphere, including those which lead to high concentrations, are not well understood thus limit our ability to accurately assess and forecast air quality. Presented here are the first long-term chemical composition measurements from an urban environment using an Aerodyne compact Time-of-Flight Aerosol Mass Spectrometer (cToF-AMS). Organic aerosols (OA) were observed to account for a significant fraction (44%) of the total non-refractory submicron mass during 2012 at the urban background site in North Kensington, London, followed by nitrate (28%), sulphate (14%), ammonium (13%), and chloride (1%). The sources and components of OA were determined using Positive Matrix Factorisation (PMF) and attributed as hydrocarbon-like OA (HOA), cooking OA (COA), solid fuel OA (SFOA), type 1 oxygenated OA (OOA1), and type 2 oxygenated OA (OOA2), where HOA, COA, and SFOA were observed to be of equal importance across the year. The concentration of secondary OA increased during the summer yet the extent of oxidation, as defined by the oxygen content, showed no variability during the year. The main factors governing the diurnal, monthly, and seasonal trends observed in all organic and inorganic species were meteorological conditions, specific nature of the sources, and availability of precursors. Regional and transboundary pollution influenced total aerosol concentrations and high concentration events were observed to be governed by different factors depending on season. High-Resolution ToF-AMS measurements were used to further probe OA behaviour, where two SFOA factors were derived from PMF analysis in winter, which likely represent differences in burn conditions. In the summer an OA factor was identified, likely of primary origin, which was observed to be strongly associated with organic nitrates and anthropogenic emissions. This work uses instruments and techniques that have not previously been used in this way in an urban environment, where the results further the understanding of the chemical components of urban aerosols. Aerosol sources are likely to change in the future with increases in solid fuel burning as vehicular emissions decrease, with significant implications on air quality and health. Thus it is important to understand aerosol sources and behaviour in order to develop effective pollution abatement strategies.

No description available.

Ion traps used in mass spectrometers are of two classes. One class consists of traps having three electrode geometries which have rotational symmetry about central axis. They are called axially symmetric ion traps. Paul trap, Cylindrical Ion Trap(CIT) are examples in this class. Other class of traps contain 2D electric field inside them which has same profile along the central axis due to translational symmetry. Linear Ion Trap(LIT) and Rectilinear Ion Trap(RIT) are examples in this class. In the ideal hyperbolic geometries of Paul trap and LIT, electric field is a perfectly linear function of distance from the center of the trap. But when these ideal geometries are simplified in to simpler geometries of the CIT and the RIT for ease in machining, linearity of field, which is a specialty of Paul trap and LIT is lost. In this thesis, an effort is made to optimize the field within the traps by using split electrodes. The ring electrode of the CIT and both pairs of electrodes in the RIT are divided into more number of parts. Suitable voltages are applied on these parts to improve the linearity of the field. This thesis contains six chapters. Chapter 1 contains a background information about mass spectrometry. Chapter 2 discusses the Boundary Element Method (BEM) used to calculate charge distribution and Nelder-Mead method used for optimization. It also shows the calculation of multipoles. In Chapter 3, two new geometries namely split-electrode RIT and split-electrode CIT are considered with the objective of improving the linearity of electric field inside them. It is shown here that by applying certain external potential on various parts of split electrodes of these geometries, it is possible to improve the linearity of electric field inside them. In Chapter 4, capacitor models of new geometries proposed in chapter 3 are discussed. The use of external capacitors as a replacement to external power supply is also discussed in this chapter. InChapter5, study similar to that ofChapter3is carried out by splitting the geometries in more number of parts. The possibility of improved field profile is investigated by applying full potential to some of these parts and keeping other parts at ground potential. In Chapter 6, concluding remarks are discussed.

Neste trabalho foram estudados vinhos provenientes de microvinificações das variedades Merlot e Cabernet Sauvignon das sub-regiões de Pinto Bandeira, Vale dos Vinhedos, Nova Pádua e Monte Belo do Sul, nas safras de 2005 e 2006. Foram determinadas as razões isotópicas 13C/12C do etanol e 18O/16O da água e do etanol, buscando possível diferenciação entre as variedades e safras de produção, e provável relação entre o local de origem e suas características geográficas (altitude e latitude) e climatológicas (temperatura, precipitação pluviométrica e umidade). Utilizou-se um espectrômetro de massas de razão isotópica (IRMS) acoplado a um analisador elementar, para análise de 13C/12C do etanol e 18O/16O da água e a um cromatógrafo gasoso, para análise de 18O/16O do etanol. Em relação aos valores de δ13C, observou-se que a diferenciação entre as sub-regiões amostrais são menos seletivas e não seguem mesma ordem estatística encontrada para as análises δ18O, porém a análise de δ13C do etanol pode servir para diferenciar sub-regiões que não são diferenciadas estatisticamente pelas análises de δ18O. O comportamento dos valores de δ18O da água e do etanol obedecem mesma ordem estatística de diferenciação. Independente da variedade de uva utilizada neste trabalho, foi possível diferenciar as sub-regiões através da análise isotópica de δ18O, nas duas safras de produção, com exceção do Vale dos Vinhedos e Monte Belo do Sul, safra 2005, que não apresentaram diferenças estatísticas. As latitudes das diferentes sub-regiões apresentaram diferença estatística e demonstraram influência principalmente nos valores de δ18O da água. As análises de δ18O da água e do etanol do vinho mostraram-se mais seletivas e eficientes na discriminação das sub-regiões de cultivo do que as análises de δ13C do etanol. Foi observada uma forte correlação entre os valores de δ18O da água e do etanol. A altitude e a latitude influenciam principalmente os valores de δ18O da água e do etanol. As influências climáticas são mais marcantes na distinção entre safras de produção do que sub-regiões de cultivo. / In this work, wines provided by micro-winemakings of the variety Merlot and Cabernet Sauvignon of the sub-regions of Pinto Bandeira, Vale dos Vinhedos, Nova Pádua and Monte Belo do Sul in the 2005 and 2006 harvest have been studied. It has been established the isotopic ratios 13C/12C of the ethanol and 18O/16O of the water and ethanol, seeking for a possible differentiation among the varieties and production harvests, and a possible relation between the place of origin and its geographic features (altitude and latitude) and climatological conditions (temperature, precipitation and humidity). It has been used a isotope ratio mass spectrometer (IRMS) coupled to an elementar analyzer for the analysis of the 13C/12C of the ethanol and 18O/16O of the water and to a gas chromatograph for the analysis of 18O/16O of the ethanol. In relation to the values of δ13C, it is observed that the differentiation among the sampling sub-regions are less selective and do not follow the same statistical order found for the analysis of δ18O, however, the analysis of δ13C of the ethanol may be used to differentiate sub-regions that are not differentiated statistically by the analysis of δ18O. The value behaviors of δ18O of the water and the ethanol follow the same statistical order of differentiation. Regardless of the grape variety used in this work, it has been possible to differentiate the sub-regions through the isotopic analysis of the δ18O, in both production harvests, except for the Vale dos Vinhedos and Monte Belo do Sul, 2005 harvest, which did not present statistical differences. The latitudes of the different sub-regions presented statistical differences and demonstrated an influence mainly in the values of δ18O of the water. The analysis of δ18O of the water and the ethanol of the wine conveyed to be more selective and efficient in the discrimination of the cultivation sub-regions than the analysis of δ13C of the ethanol. It has been observed a strong correlation between the values of δ18O of the water and the ethanol. The altitude and latitude influence mainly the values of δ18O of the water and the ethanol. The climate influences are more noteworthy in distinguishing the production harvests than the cultivation sub-regions.

This thesis describes the design and implementation of control applications for the deposition interface and mass spectrometer. The paper describes the working principle of these devices and their hardware specifications. It also describes how the design and the conception of the application. Developed applications are tested on real devices at the end.

No description available.

A Direct Simulation Monte Carlo fluid dynamics code named FENIX has been employed to study gas flow-through properties of the inductively coupled plasma mass spectrometer (ICP-MS). Simulation data have been tested against the Navier-Stokes and heat equations in order to see if FENIX functions properly. The Navier-Stokes and heat equations have been constructed from simulation data and are compared term by term. This comparison shows that FENIX is able to correctly reproduce fluid dynamics throughout the ICP-MS simulation, with an exception immediately behind the ICP-MS sampler cone, where the continuum criterion for the Navier-Stokes equation is not met. Testing the data produced by Fenix also shows that this DSMC method correctly produces momentum and thermal boundary layer phenomenon as well. FENIX output data produce statistical fluctuations of about 2%. Limitations occur from fitting data near surfaces, incurring a relative error of about 5%, and fitting data to take second derivatives where fluid velocity gradients are steep, introducing a relative error of about 10%.

No description available.

O Brasil possui a sétima maior reserva geológica de urânio do mundo, com aproximadamente 310 mil toneladas. A Província Uranífera de Lagoa Real, na região de Caetité e Lagoa Real, situado no centro sul da Bahia, é considerada a mais importante província monominerálica do Brasil. A população urbana que vive no distrito uranífero nas cidades de Caetité, Lagoa Real e Livramento de Nossa Senhora usa água potável oriunda do abastecimento público. Na área rural, caracterizada por freqüentes secas, os moradores recebem água de poços escavados e perfurados como também, de pequenas barragens e reservatórios abastecidos pelas chuvas. Este trabalho determinou os níveis de radioatividade alfa e beta total e as concentrações de urânio em diversos tipos de água consumidas pela população urbana e rural da Província Uranífera de Lagoa Real. As atividades α e β total foram determinadas com detector proporcional de fluxo gasoso e baixa radiação de fundo. As concentrações de urânio foram determinadas com o Espectrômetro de Massa com Fonte de Plasma Indutivo (ICP-MS). Os resultados obtidos foram comparados com as recomendações recentes de 2011 da Organização Mundial da Saúde, a portaria nº 2914 de 12/12/2011 do Ministério da Saúde e as resoluções do CONAMA. Os níveis de radiação natural variaram de 0,0041 ± 0,0004 Bq.L-1 a 0,80 ± 0,04 Bq.L-1 para a atividade alfa total e de 0,045 ± 0,003 a 3,0 ± 0,2 Bq.L-1 para a atividade beta total. Tendo como parâmetro a OMS e o MS, apenas duas amostras de água subterrânea, uma localizada na cidade de Lagoa Real e outra na cidade de Caetité apresentaram concentrações alfa total acima do valor de 0,5 Bq.L-1 descrito em suas recomendações, 0,80 ± 0,04 Bq.L-1 e 0,57 ± 0,03 Bq.L-1respectivamente. Para beta total, três amostras apresentaram níveis de radioatividade acima do limite de 1 Bq.L-1 recomendado pela Organização Mundial de Saúde e estabelecido pelo Ministério da Saúde; 3,0 ± 0,2 Bq.L-1; 1,63 ± 0,13 Bq.L-1 e 1,19 ± 0,07 Bq.L-1 todos situados no município de Lagoa Real. Duas amostras de água subterrânea no município de Caetité apresentaram concentrações de urânio acima do valor de 15 μg.L-1 determinado pelo CONAMA, 20,3 ± 0,3 μg.L-1 e 17,1± 0,3 μg.L-1. Em Lagoa Real, uma amostra apresentou níveis de urânio seis vezes superior ao limite estabelecido pelo Conselho Nacional de Meio Ambiente, 89,5 ± 1,5 μg.L-1. A Organização Mundial da Saúde em 2004 estabeleceu em suas recomendações o limite de 15 μg.L-1 como a concentração máxima de urânio na água potável. Em 2011 a OMS aumentou este limite para 30 μg.L-1. Levando-se em consideração as atuais recomendações da OMS, apenas a concentração de uma amostra de água apresentou níveis de urânio acima do recomendado, 89,5 ± 1,5 μg.L-1 no município de Lagoa Real. / Brazil has the seventh greatest geological uranium reserve in the world with approximately 310 thousand tons. The Lagoa Real Uranium Province, in the region of Caetité and Lagoa Real, situated in South Center Bahia, is considered the most important monomineralic province in Brazil. Urban population who lives in the uranium district in the cities of Caetité, Lagoa Real and Livramento de Nossa Senhora uses drinking water originated from public supply. In the rural area, characterized by frequent draughts, residents receive water from digged and drilled wells and from small dams and reservoirs, as well, which are supplied by the rains. This work determined the levels of total alpha and beta radioactivity and the uranium concentrations in several kinds of water consumed by urban and rural population from the Lagoa Real Uranium Province. Total α e β activities were determined with a low-level gas flow proportional detector. The uranium concentrations were determined with an inductive coupled plasma-mass spectrometer (ICP-MS). The results obtained were confronted with the latest World Health Organizations recommendations from 2011, the ordinance number 2914 of December 12 2011 from the Health Ministry and CONAMAs resolutions. Natural radiation levels varied from 0,0041 ± 0,0004 Bq.L-1 to 0,80 ± 0,04 Bq.L-1 for total alpha activity and from 0,045 ± 0,003 to 3,00 ± 0,2 Bq.L-1 for total beta activity. Having the WHO and the HM as parameter, just two underground water samples, one located in the city of Lagoa Real and the other in the city of Caetité presented total alpha concentration above the value of 0,5 Bq.L-1 described in its recommendations, 0,80 ± 0,040 Bq.L-1 and 0,57 ± 0,03 Bq.L-1 respectively. For total beta three samples presented radioactivity levels above the 1 Bq.L-1 limit recommended by the WHO and established by the Health Ministry; 3,00 ± 0,2 Bq.L-1; 1,63 ± 0,13 Bq.L-1 and 1,19 ± 0,07 Bq.L-1., all of them situated in the Lagoa Real town. Two samples of underground water from Caetité presented uranium concentrations above the value of 15 μg.L-1 determined by CONAMA, 20,3 ± 0,3 μg.L-1 and 17,1± 0,3 μg.L-1. In Lagoa Real one sample presented uranium levels six times over the limit established by the Environment National Council 89,5 ± 1,5 μg.L-1. In 2004 the World Health Organization established in its recommendations the 15 μg.L-1 limit as the maximum uranium concentration in drinking water. In 2011 the WHO increased that limit to 30 μg.L-1. Taking into account the current WHO recommendations only the concentration of one water sample presented uranium levels above the recommended, 89,5 ± 1,5 μg.L-1 in Lagoa Real.