Opalas gemológicas do Piauí: gênese revelada por microtermometria e minerais associados

As opalas de Pedro II e Buriti dos Montes, no estado do Piauí, constituem as mais importantes ocorrências brasileiras dessa gema, tanto em termos de volume quanto pela qualidade gemológica, que é comparável à das famosas opalas australianas. No entanto, a informalidade na extração e comercialização destas opalas, assim como a falta de informações quanto à gênese destes depósitos não permitem a prospecção por novas jazidas e o estabelecimento de um certificado de procedência para as opalas do Piauí que permitisse sua inserção formal no mercado gemológico internacional. Alguns autores têm se dedicado ao estudo dessas opalas, revelando fortes evidências de sua origem hidrotermal, mas até então, nenhum trabalho abordou as características físico-químicas dos fluidos que teriam originado esses depósitos de opalas. Diante disso, o principal objetivo deste trabalho foi entender o sistema hidrotermal responsável pela gênese das opalas do Piauí, ou seja, caracterizar os fluidos que originaram a mineralização e mostrar sua relação com o contexto geológico da região. Os municípios de Pedro II e Buriti dos Montes se localizam na porção nordeste do estado do Piauí, a aproximadamente 230 km a leste da capital Teresina, e as ocorrências de opala se encontram na porção basal da Bacia do Parnaíba, constituindo veios e vênulas nos arenitos dos grupos Serra Grande (Buriti dos Montes) e Canindé (Pedro II), os quais são seccionados por soleiras e diques de diabásio da Formação Sardinha. Elas também ocorrem cimentando brechas e como depósitos coluvionares e de paleocanal. Associados às opalas, localmente encontram-se veios de quartzo, calcedônia, barita e hematita (ou goethita). De maneira geral, as opalas de Pedro II apresentam jogo de cores, são predominantemente brancas ou azuladas com aspecto leitoso, semitranslúcidas a opacas e com inclusões sólidas pouco aparentes. Em contrapartida, as opalas de Buriti dos Montes não apresentam jogo de cores, a cor varia entre amarelo claro e vermelho amarronzado, são semitransparentes a translúcidas e contêm grande variedade de inclusões sólidas. Os dados obtidos revelam que as opalas de Pedro II são tipicamente do tipo amorfo (opala-A), enquanto as opalas de Buriti dos Montes variam entre amorfas e cristobalita-tridimita (opala-CT). Na opala preciosa, o típico jogo de cores é causado pelo arranjo regular das esferas de sílica que as constituem. A ausência de cimento opalino entre as esferas reforça a beleza desse efeito. Em contrapartida, as opalas laranja não apresentam jogo de cores, mas têm maior transparência devido ao diminuto tamanho das esferas. As inclusões sólidas também produzem belos efeitos nas opalas estudadas, principalmente na variedade laranja, que é mais transparente. Além disso, o conjunto de inclusões sólidas revela características intrínsecas aos processos hidrotermais que originaram as opalas estudadas. Agregados botrioidais, dendríticos e nodulares são exemplos de inclusões formadas por fragmentos dos arenitos hospedeiros carreados pelos fluidos hidrotermais que geraram as opalas. As inclusões sólidas também têm relação direta com a cor das opalas. Nas opalas de Buriti dos Montes, os tons de vermelho, laranja e amarelo são produzidos pela dissolução parcial das inclusões constituídas por oxihidróxidos de Fe. De maneira semelhante, a cor verde nas opalas preciosas está relacionada aos microcristais de Co-pentlandita inclusos nas mesmas. O conjunto de minerais associados às opalas conduz a uma assinatura mineralógicogeoquímica marcada pelos elevados teores de Fe e Al nas opalas com inclusões de hematita/goethita e caulinita, e assim também com aumento considerável dos teores de elementos terras raras nas opalas em que se concentram as inclusões de caulinita e apatita. Entre os elementos-traço, Ba é o mais abundante, e provavelmente foi incorporado pelo fluido hidrotermal, tendo em vista que veios de barita são encontrados com frequência nessa região da Bacia do Parnaíba. Várias feições como estruturas de fluxo nas opalas, corrosão e dissolução parcial dos cristais de quartzo hialino e de inclusões mineralógicas, vênulas de quartzo hidrotermal sobrecrescidas aos grãos detríticos, e zoneamento dos cristais de quartzo confirmam que essas opalas têm origem hidrotermal. A ruptura do Gondwana teria provocado um vasto magmatismo básico fissural, que por sua vez foi responsável pelo aporte de calor que gerou as primeiras células convectivas de fluidos quentes. A água contida nos arenitos certamente alimentou o sistema e se enriqueceu em sílica através da dissolução parcial ou total dos próprios grãos de quartzo dos arenitos. Este fluido hidrotermal foi posteriormente aprisionado em sistemas de fraturas e nelas se resfriou, precipitando a opala e minerais associados.

Uso da padronização interna em espectrometria de absorção atômica em forno de grafite na determinação de 'SE' e 'NI' em bebidas não alcoólicas

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Obtenção e avaliação das potencialidades biológicas de complexos metálicos de 'ZN' e 'CO' contendo proteínas hidrolisadas do soro do leite

Pós-graduação em Química - IQ

Soil microbial biomass after two years of the consecutive application of composted tannery sludge

Because the agricultural use of tannery sludge may cause increased risks to soils, composting is recognized as one of the most suitable alternative for tannery sludge recycling. Experiments were conducted under field conditions to evaluate the effects of composted tannery sludge (CTS) on the soil microbial biomass and trace elements after two years of consecutive applications. The following five treatments were used: 0 (without CTS application), 5, 10, 20 and 40 ton ha-1 of CTS (dry basis). Soil samples were collected at 60 days after the CTS application at 0-20 cm depth. The CTS application promoted changes in the soil microbial biomass C (SMB-C) and N (SMB-N). In the first year, significant increases in the SMB-C and SMB-N were observed with the application of 10 ton ha-1. Furthermore, CTS application increased the Cr content in the soil after two years of application.

Cross linked Poly (4-Vinylpyridine-Ethylene Glycol Dimethacrylate) Used for Preconcentration of Cd(II) and its Determination by Flow Injection Flame Atomic Absorption Spectrometry

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Heavy metals in cowpea (Vigna unguiculata L.) after tannery sludge compost amendment

Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq)

Heavy metals and yield of cowpea cultivated under composted tannery sludge amendment

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

Blood and seminal plasma concentrations of selenium, zinc and testosterone and their relationship to sperm quality and testicular biometry in domestic cats

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

Elementos-traço em dois latossolos após aplicações anuais de lodo de esgoto por treze anos

This experiment aim was to evaluate the contamination of the trace elements (TE) arsenic, barium, cadmium, chromium, copper, mercury, molybdenum, nickel, lead, selenium, and zinc considered in the CONAMA resolution 375 after 13 years long using sewage sludge (SS) as fertilizer in two soils: an Eutroferric Clayed Red Latosol (Rhodic Eutrudox - RE) and a Dystrophic Red Latosol (Typic Haplorthox - TH). Experiment in the field under maize cultivation had four treatments (0, 5, 10, and 20 t of SS ha(-1), dry weight), five replications and an experimental design in randomized blocks. The agrochemicals (dolomitic limestone, single superphosphate, and potassium chloride), SS, soils, and the certified reference materials were digested according to the USEPA 3051A method and the chemical elements were quantified by ICP OES. The TE contents found in the agrochemicals used should not cause immediate environmental impact. The higher TE values were found in the RE and they did not reach the agricultural (more stringent) Investigation Level (IL) yet, according to 420 CONAMA resolution. Persisting the actual SS fertilization amount applied in the soil and the TE concentration in the SS is foreseen that Ba, Cd, Cr, Cu, Ni, and Zn will be the first elements to reach the IL in the RE.

Quimioestratigrafia do vulcanismo ácido mesozóico da província magmática do Paraná: porção SE do estado de Santa Catarina

The Mesozoic acid volcanism of the Paraná-Etendeka Province can be considered as one of the biggest events of its kind in the Earth's surface, and its study have attracted special interest in characterizing the end of magmatism that preceded the rupture process and the formation of continental Africa and South America Although significant, the acid volcanism featuring Members Chapecó Palmas and Serra Geral Formation represents only 2.5% of the total generated by the magmatic rocks and perhaps therefore the existing literature on these rocks is well less significant than that on the basalts. However, there are still aspects still unclear about the origin and evolution of these rocks in relation to the associated basalts. Thus, two profiles were selected, called RA and TA, which be a systematic collection of samples from the base where the Botucatu Formation sandstones occur at the top, where they observe Palmas acid rock type. These samples should be analyzed for major, minor and trace elements and treated in specific diagrams to define the vertical variation lithochemistry and their possible relationships with the associated basalts

A simple method based on ICP-MS for estimation of background levels of arsenic, cadmium, copper, manganese, nickel, lead, and selenium in blood of the Brazillian population

Throughout the world, biomonitoring has become the standard for assessing exposure of individuals to toxic elements as well as for responding to serious environmental public health problems. However, extensive biomonitoring surveys require rapid and simple analytical methods. Thus, a simple and high-throughput method is proposed for the determination of arsenic (As), cadmium (Cd), copper (Cu), manganese (Mn), nickel (Ni), lead (Pb), and selenium (Se) in blood samples by using inductively coupled plasma–mass spectrometry (ICPMS). Prior to analysis, 200 ml of blood samples was mixed with 500 ml of 10% v/v tetramethylammonium hydroxide (TMAH) solution, incubated for 10 min, and subsequently diluted to 10 ml with a solution containing 0.05% w/v ethylenediamine tetraacetic acid (EDTA) + 0.005% v/v Triton X-100. After that, samples were directly analyzed by ICP-MS (ELAN DRC II). Rhodium was selected as an internal standard with matrix-matching calibration. Method detection limits were 0.08, 0.04, 0.5, 0.09, 0.12, 0.04, and 0.1 mg//L for As, Cd, Cu, Mn, Ni, Pb, and Se, respectively. Validation data are provided based on the analysis of blood samples from the trace elements inter-\comparison program operated by the Institut National de Santé Publique du Quebec, Canada. Additional validation was provided by the analysis of human blood samples by the proposed method and by using electrothermal atomic absorption spectrometry (ETAAS). The method was subsequently applied for the estimation of background metal blood values in the Brazilian population. In general, the mean concentrations of As, Cd, Cu, Mn, Ni, Pb, and Se in blood were 1.1, 0.4, 890, 9.6, 2.1, 65.4, and 89.3 mg/L, respectively, and are in agreement with other global populations. Influences of age, gender, smoking habits, alcohol consumption, and geographical variation on the values were also considered. Smoking habits influenced the levels of Cd in blood. The levels of Cu, Mn, and Pb were significantly correlated with gender, whereas Cu and Pb were significantly correlated with age. There were also interesting differences in Mn and Se levels in the population living in the north of Brazil compared to the south.

Fracionamento geoquímico de metais em sedimentos e avaliação da qualidade da água do Rio Bento Gomes, Pantanal de Poconé, Mato Grosso

Pós-graduação em Química - IQ

Chromium in soil organic matter and cowpea after four consecutive annual applications of composted tannery sludge

Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES)

Hydrochemical and stable isotopes (H, O, S) signatures in deep groundwaters of Parana basin, Brazil

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

Homogeneity of the geochemical reference material BRP-1 (paranábasin basalt) and assessment of minimum mass

Reference materials (RM) are required for quantitative analyses and their successful use is associated with the degree of homogeneity, and the traceability and confidence limits of the values established by characterisation. During the production of a RM, the chemical characterisation can only commence after it has been demonstrated that the material has the required level of homogeneity. Here we describe the preparation of BRP-1, a proposed geochemical reference material, and the results of the tests to evaluate its degree of homogeneity between and within bottles. BRP-1 is the first of two geochemical RM being produced by Brazilian institutions in collaboration with the United States Geological Survey (USGS) and the International Association of Geoanalysts (IAG). Two test portions of twenty bottles of BRP-1 were analysed by wavelength dispersive-XRF spectrometry and major, minor and eighteen trace elements were determined. The results show that for most of the investigated elements, the units of BRP-1 were homogeneous at conditions approximately three times more rigorous than those strived for by the test of sufficient homogeneity. Furthermore, the within bottle homogeneity of BRP-1 was evaluated using small beam (1 mm(2)) synchrotron radiation XRF spectrometry and, for comparison, the USGS reference materials BCR-2 and GSP-2 were also evaluated. From our data, it has been possible to assign representative minimum masses for some major constituents (1 mg) and for some trace elements (1-13 mg), except Zr in GSP-2, for which test portions of 74 mg are recommended.