RESUMO

Herbicide use, mainly glyphosate, has been intense in worldwide agriculture, including in the Brazilian Amazon region. This study aimed to validate a method for determining glyphosate and its degradation product, AMPA, and glufosinate by HPLC-FL in 58 water samples collected at the Santarém plateau region (Planalto Santareno), in the western of Pará state, Brazil. The method involves filtration and direct injection in the HPLC-FL for AMPA analysis, or previous concentration (10×) by lyophilization for glufosinate and glyphosate analysis. Analytes were oxidized and complexed with o-phthalaldehyde and 2-mercaptoethanol in a post-column reaction before fluorescence detection. LOQs for AMPA, glyphosate and glufosinate were established at 0.5, 0.2 and 0.3 µg L-1, respectively. A total of 58 samples were collected. Glyphosate and glufosinate were not detected in any of the 30 surface water samples collected in 2015 (

Assuntos

RESUMO

Numerous articles have reported the occurrence of arsenic in drinking water in Argentina, and the resulting health effects in severely affected regions of the country. Arsenic in drinking water in Argentina is largely naturally occurring due to elevated background content of the metalloid in volcanic sediments, although, in some regions, mining can contribute. While the origin of arsenic release has been discussed extensively, the problem of drinking water contamination has not yet been solved. One key step in progress towards mitigation of problems related with the consumption of As-containing water is the availability of simple detection tools. A chemical test kit and the ARSOlux biosensor were evaluated as simple analytical tools for field measurements of arsenic in the groundwater of Rafaela (Santa Fe, Argentina), and the results were compared with ICP-MS and HPLC-ICP-MS measurements. A survey of the groundwater chemistry was performed to evaluate possible interferences with the field tests. The results showed that the ARSOlux biosensor performed better than the chemical field test, that the predominant species of arsenic in the study area was arsenate and that arsenic concentration in the studied samples had a positive correlation with fluoride and vanadium, and a negative one with calcium and iron.

Assuntos

RESUMO

The aim of this study was to investigate the relationship between the concentrations of heavy metals in well water and bioaccumulation of the most abundant metals in chicken tissues in some areas in the province of Mecca Almokaramah, Saudi Arabia. Among the heavy metals (Cd, Zn, Cr, Mn, Cu Hg, Pb and Ni) studied, mercury (Hg) revealed highest in concentration in well waters. The concentration of mercury in the ground water, beside in liver, kidney, muscle and blood samples of ten chickens from each of four poultry- production farms were estimated using atomic absorption spectrophotometer. The results showed that the kidney followed by liver had the highest bioaccumulation of mercury in all farm samples. The level of mercury in the ground water was 7.06µg/L. The relationship between mercury accumulation levels in the kidney and those in the liver tissues were proportionally correlated and altered with elevation in the antioxidant enzyme activities such as AST and ALT. These elevated enzymatic activities were induced by the level of toxicity. There was a significant elevation in the level of liver and kidney malondialdhyde (MDA), while the activities of antioxidant enzymes superoxide dismutase and catalase (SOD and CAT) were significantly decreased. Biochemical observations were supplemented by histopathological examination of liver and kidney sections.

RESUMO

Anomalous concentrations of hexavalent chromium have been detected in ground-water of the Adamantina Aquifer inat least 54 municipalities located in the northwestern region of the State of São Paulo, southeast Brazil, occasionallyexceeding the permitted limit for human consumption (0.05 mg.L-1). An investigation was conducted in the municipality of Urânia, where the highest concentrations of chromium were detected regionally. It was defined that the originof this contamination is natural, since high concentrations of chromium were detected in aquifer sandstones (averageof 221 ppm) and also in pyroxenes (6000 ppm), one of the main heavy minerals found in the sediments. Besides, noother possible diffuse or point sources of contamination were observed in the study area. Stratification of ground-waterquality was observed and the highest concentrations of Cr6+ were detected at the base of the aquifer (0.12 mg.L-1),where ground-water shows elevated values for redox potential (472.5 mV) and pH (8.61). The origin of Cr6+ in water may be associated with the weathering of pyroxene (augite), followed by the oxidation of Cr3+ by manganese oxides. The highest concentrations of Cr6+ are probably related to desorption reactions, due to the anomalous alkaline pHfound in ground-water at the base of the aquifer.

Concentrações anômalas de cromo hexavalente foram detectadas em águas subterrâneas do Aqüífero Adamantina em pelo menos 54 municipalidades localizadas na região noroeste do Estado de São Paulo, sudeste do Brasil, algumas vezes ultrapassando o limite máximo permitido para consumo humano (0,05 mg.L-1). Um estudo foi realizado no município de Urânia, onde as mais elevadas concentrações de cromo da região foram detectadas. A origem da contaminação foi definida como natural, pois foram detectadas concentrações de cromonos arenitos do aqüífero (média 221 ppm) e em piroxênios (6000 ppm), um dos principais minerais pesados encontrados nos sedimentos. Além disso, não foram observadas outras possíveis fontes de contaminação difusas ou pontuais naárea de estudo. Uma estratificação da qualidade da água no aqüífero foi observada e as mais elevadas concentrações de Cr6+ foram detectadas na base do aqüífero (0,12 mg.L-1), onde as águas subterrâneas apresentam valores elevados de potencial redox (Eh = 472,5 mV) e de pH (8,61). A origem do Cr6+ na água deve estar associada com o intemperismo do piroxênio (augita), seguida da oxidação do Cr3+ pelos óxidos de manganês. As maiores concentrações de Cr6+ estão provavelmente ligadas com reações de desorção, devido ao pH anomalamentealcalino da água subterrânea na base do aqüífero.