Levels of cadmium, mercury, and lead in Magellanic penguins (Spheniscus magellanicus) stranded on the Brazilian coast.

Cadmium (Cd), mercury (Hg), and lead (Pb) were determined in samples of liver and breast muscles of first-year Magellanic penguins (Spheniscus magellanicus), from two different areas on the Brazilian coast, 35 on the Rio de Janeiro coast and 12 on the Rio Grande do Sul coast. In both areas, Cd concentrations in muscle samples were <0.025 microg/g. However, the Cd and Hg concentrations found in liver and Hg concentrations found in muscle showed a significant difference between the two regions. The geometric mean of the concentrations was higher in the specimens from Rio de Janeiro (Cd--6.8 microg/g; Hg--liver, 1.6 microg/g, and muscle, 0.4 microg/g wet weight) than in those from Rio Grande do Sul (Cd--2.3 microg/g; Hg--liver, 0.9 microg/g, and muscle, 0.1 microg/g wet weight). The site differences could be related to differences in diet influenced by geographic factors. Brazil's southeastern coast is highly urbanized, and its coastal waters are contaminated by the waste of agricultural and industrial activities. There is a lack of information on the levels of heavy metals in S. magellanicus, however, their wide distribution and top position in the trophic chain make the use of stranded specimens an attractive source of information for monitoring heavy metals in the South Atlantic coast.

An overview of mercury contamination research in the Amazon basin with an emphasis on Brazil.

This article provides an overview of research on mercury contamination in the Amazon Basin and its evolution from 1990 to 2005. The assessment was based on an extensive and systematic review using bibliographic databases available online and a review of projects by research groups. Brazilian research groups were identified using the database of the Brazilian National Research Council (CNPq). A geographic information system was used to determine the location of the studies. Different aspects of mercury contamination were evaluated (environmental studies, impacts on human health, technological improvements). For 1990-2005, a total of 455 publications were identified. The main advances and remaining gaps in relation to environmental issues and human health were identified and discussed. Although the scientific output varied considerably over the period, there was a general increase in the total number of publications per year from the early 1990s (fewer than 20) until 2005 (more than 30), considering the articles published in indexed journals.

Non-chromatographic speciation of toxic arsenic in vegetables by hydride generation-atomic fluorescence spectrometry after ultrasound-assisted extraction.

A non-chromatographic, sensitive and simple analytical method has been developed for the determination of toxic arsenic species in vegetable samples by hydride generation-atomic fluorescence spectrometry (HG-AFS). As(III), As(V), dimethylarsinic acid (DMA) and monomethylarsonic acid (MMA) were determined by hydride generation-atomic fluorescence spectrometry using a series of proportional equations. The method is based on a single extraction of the arsenic species considered from vegetables through sonication at room temperature with H(3)PO(4) 1 mol L(-1) in the presence of 0.1% (w/v) Triton XT-114 and washing of the solid phase with 0.1% (w/v) EDTA, followed by direct measurement of the corresponding hydrides in four different experimental conditions. The limit of detection of the method was 3.1 ng g(-1) for As(III), 3.0 ng g(-1) for As(V), 1.5 ng g(-1) for DMA and 1.9 ng g(-1) for MMA, in all cases expressed in terms of sample dry weight. Recovery studies provided percentages greater than 91% for all considered species in spiked samples of chards and aubergines. Total toxic As found in the aforementioned samples was at the level of 90 ng g(-1); As(III) is followed by As(V), DMA and MMA which are the main species of As in chards being As(V) the main As compound in aubergines.

An overview of mercury contamination research in the Amazon basin with an emphasis on Brazil / Uma revisão das pesquisas sobre contaminação por mercúrio na Amazônia com ênfase no território brasileiro

This article provides an overview of research on mercury contamination in the Amazon Basin and its evolution from 1990 to 2005. The assessment was based on an extensive and systematic review using bibliographic databases available online and a review of projects by research groups. Brazilian research groups were identified using the database of the Brazilian National Research Council (CNPq). A geographic information system was used to determine the location of the studies. Different aspects of mercury contamination were evaluated (environmental studies, impacts on human health, technological improvements). For 1990-2005, a total of 455 publications were identified. The main advances and remaining gaps in relation to environmental issues and human health were identified and discussed. Although the scientific output varied considerably over the period, there was a general increase in the total number of publications per year from the early 1990s (fewer than 20) until 2005 (more than 30), considering the articles published in indexed journals.

Esta pesquisa apresenta uma visão geral dos estudos desenvolvidos sobre a contaminação por mercúrio na bacia Amazônica e a evolução destes estudos no período 1990-2005. O estudo baseou-se em extensiva e sistemática revisão utilizando bases de dados bibliográficas disponíveis na Internet e em uma revisão dos projetos de pesquisa realizados por grupos de pesquisa. Além disso, os grupos de pesquisa brasileiros foram identificados pela base de dados do Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq). Um sistema de informação geográfica foi usado para localizar os estudos conduzidos. Diferentes aspectos da contaminação por mercúrio na Amazônia foram analisados (estudos ambientais, impactos na saúde humana, melhorias tecnológicas). No período de 1990-2005, foram identificadas 455 publicações. As principais realizações e as lacunas existentes em relação aos estudos ambientais e de saúde humana foram identificadas e discutidas. Apesar de variações, há um aumento geral do número total de publicações por ano desde o começo da década de 1990 (menos de 20) para o final do período estudado (mais de 30), expresso por meio dos artigos publicados em revistas indexadas.

Antifungal Pisum sativum defensin 1 interacts with Neurospora crassa cyclin F related to the cell cycle.

Plant defensins, components of the plant innate immune system, are cationic cysteine-rich antifungal peptides. Evidence from the literature [Thevissen, K., et al. (2003) Peptides 24, 1705-1712] has demonstrated that patches of fungi membrane containing mannosyldiinositolphosphorylceramide and glucosylceramides are selective binding sites for the plant defensins isolated from Dahlia merckii and Raphanus sativus, respectively. Whether plant defensins interact directly or indirectly with fungus intracellular targets is unknown. To identify physical protein-protein interactions, a GAL4-based yeast two-hybrid system was performed using the antifungal plant peptide Pisum sativum defensin 1 (Psd1) as the bait. Target proteins were screened within a Neurospora crassa cDNA library. Nine out of 11 two-hybrid candidates were nuclear proteins. One clone, detected with high frequency per screening, presented sequence similarity to a cyclin-like protein, with F-box and WD-repeat domains, related to the cell cycle control. GST pull-down assay corroborated in vitro this two-hybrid interaction. Fluorescence microscopy analysis of FITC-conjugated Psd1 and DAPI-stained fungal nuclei showed in vivo the colocalization of the plant peptide Psd1 and the nucleus. Analysis of the DNA content of N. crassa conidia using flow cytometry suggested that Psd1 directed cell cycle impairment and caused conidia to undergo endoreduplication. The developing retina of neonatal rats was used as a model to observe the interkinetic nuclear migration during proliferation of an organized tissue from the S toward the M phase of the cell cycle in the presence of Psd1. The results demonstrated that the plant defensin Psd1 regulates interkinetic nuclear migration in retinal neuroblasts.

Determination of copper and nickel in vegetable oils by direct sampling graphite furnace atomic absorption spectrometry.

The quality of food products has been receiving great attention due to its influence on human nutrition and health. In this sense, the determination of trace metals in foods has turned an important field on food analysis. Concerning vegetable oils, its metal trace composition is an important criterion for the assessment of their quality once it is known that trace metals affect their rate of oxidation, influencing freshness, keeping properties as well as storage. In the present work an analytical method which enables the direct determination of Cu and Ni in vegetable oils by graphite furnace atomic absorption spectrometry (GFAAS), using a "solid" sample strategy is presented: in nature, samples are directly weighed on the graphite platform boat and inserted in the graphite tube. An adequate temperature program permitted the calibration by external aqueous analytical curves. Good concordance between the proposed procedure and EPA procedures was found in the analysis of real samples. Limits of detection of 0.001 and 0.002mugg(-1) were found for Cu and Ni, respectively, in the original samples, and they were comfortably below the concentrations found.

The determination of molybdenum in water and biological samples by graphite furnace atomic spectrometry after polyurethane foam column separation and preconcentration.

A system for molybdenum separation and enrichment aiming its determination in water and biological samples by graphite furnace atomic absorption spectrometry (GFAAS) is proposed. The procedure is based on the sorption of the molybdenum (VI) thiocyanate complex onto a mini-column packed with polyurethane foam (PUF). The elution is accomplished by a 3.0 mol l(-1) nitric acid solution. Flow variables were optimized and an enrichment factor of 10 as well as a limit of detection (LOD) (3 s) of 0.08 mug l(-1) in the sample solution were achieved. The coefficient of variation showed values of 3 and 2% for molybdenum solutions of 2.0 and 10.0 mug l(-1), respectively. The accuracy of the method was confirmed by the good concordance between found and certified values in the analysis of certified reference materials (CRMs) (CASS-3 Nearshore Seawater, NIST 1547 Peach Leaves, NIST 1515 Apple Leaves and NIST 1572 Citrus Leaves). The procedure was also applied for the molybdenum determination in mineral waters as well as in produced water samples. The results obtained for the mineral water samples compared well with those obtained by ICP-MS. Concerning the produced water samples, in spite of their large salinity, recoveries of 90 to 120% at the 1 mug l(-1) were observed.

Cadmium uptake by hydroxyapatite synthesized in different conditions and submitted to thermal treatment.

This paper intends to evaluate the uptake of cadmium ions from aqueous solution by 21 hydroxyapatite samples which have been synthesized in different conditions. It has been determined thatthe variation on the hydroxyapatite sorption capacity is neither related to sample solubility nor to hydroxyapatite Ca/P molar ratio. Cd2+ sorption is controlled by sample BET surface area, which shows a direct dependence on the hydroxyapatite crystallite dimensions. The hydroxyapatite pore distribution presented modes at 1000 and 60,000 A, corresponding to intracrystallite voids and voids between the agglomerate of these crystallites, respectively. Pores belonging to the former mode immobilize the major part of Cd2+. The influence of sample thermal treatment on Cd2+ sorption efficiency has been studied using hydroxyapatite samples calcined at temperatures ranging from 500 to 1140 degrees C. Similarly to nonthermally treat samples, the Cd2+ sorption on calcined hydroxyapatite could be described by Langmuir isotherms. The results showed that the maximum sorption capacity decreased from 0.631 mmol g(-1) for the noncalcined sample to 0.150 mmol g(-1) for the one calcined at 900 degrees C. This drop in the sorption capacity could also be explained by a reduction in its specific surface area, which is induced bythe increase of the crystal size.

Estudo comparativo dos efeitos da utilizaçao de mercúrio por dentistas / Comparative study on the effects of mercury utilization by dentists

Foi realizado um estudo comparativo dos efeitos do mercúrio entre dentistas e médicos que trabalhamna Universidade Federal do Rio de Janeiro. Os resultados obtidos mostraram que os dentistas apresentavam um número estatisticamente maior de morbidade referida por rins e aparelho digestivo e sinais e sintomas de alteraçoes de sistema nervoso. Outrossim, nao houve diferenças significativas entre os dois grupos em relaçao aos teores de mercúrio no cabelo, o que pode ser explicado por alteraçoes recentes no processo de trabalho dos dentistas

Teores de mercúrio no cabelo: um estudo comparativo em trabalhadores da lavoura de cana-de-açucar com exposiçäo pregressa aos fungicidas organo-mercuriais no município de Campos - RJ / Levels of mercury in the hair: a comparative study in agricultural workers of sugar caane platations previons exposureto the organo-mercurial fungicidas in the municpality of Campos - RJ

Como parte de uma tese de doutoramento, foi realizado um estudo comparativo dos teores de mercúrio no cabelo de un grupo de trabalhadores que tinham deixado de manipular os fungicidas organo-mercuriais há pelo menos dois anos com outro semelhante, porém sem a história de manipulaçäo prévia destes fungicidas. Embora näo tenham sido encontradas diferenças estatisticamente significantes entre os grupos, os dados apresentados sugerem que pode ter havido contaminaçäo ambiental por mercúrio em trabalhadores, pelo menos dois anos depois da proibiçäo do uso dos fungicidas organo-mercuriais no Brasil