Aims Phytosiderophore-chelated Zn can be absorbed in grasses. Root exudates of dicotyledonous plants can mobilize soil Zn but it is unclear how this affects Zn bioavailability. Stable Zn isotope shifts can indicate exudate-facilitated Zn uptake, since complexation of Zn 2+ by organic ligands in solution yields a small, but detectable, enrichment of the heavy Zn isotope due to thermodynamic fractionation. Methods Tomato seedlings were grown in resinbuffered nutrient solution in which free Zn 2+ concentrations are buffered, in a factorial design of two Zn levels and two solution volumes. The latter factor allowed altering the exudate concentrations in the solution. Dissolved Cu concentrations in the resin buffered system were used as a sensitive index of metal mobilization resulting from root activity. In addition, seedlings were grown in Zn deficient soil with and without Zn addition. Results The dissolved Cu concentration increased with Zn deficiency and was highest at the lowest solution volume, suggesting metal mobilization by root exudates. At low Zn supply, Zn in the plant was enriched in heavy Zn (66 Zn) and this was most pronounced at small solution volume. Similarly, Zn deficiency in soil enriched tomato shoot Zn with heavy isotope in this plant. Interpretation Zinc deficiency increases the contribution of Zn-exudate complexes, which are enriched in the heavy isotope compared to the free ion, to Zn uptake by transporting Zn from the bulk solution or soil to the roots where they likely dissociate and release Zn 2+ .

Non-alcoholic fatty liver disease (NAFLD), defined by the American Liver Society as the buildup of extra fat in liver cells that is not caused by alcohol, is the most common liver disease in North America. Obesity and type 2 diabetes are viewed as the major causes of NAFLD. Environmental contaminants have also been implicated in the development of NAFLD. Northern populations are exposed to a myriad of persistent organic pollutants including polychlorinated biphenyls, organochlorine pesticides, flame retardants, and toxic metals, while also affected by higher rates of obesity and alcohol abuse compared to the rest of Canada. In this study, we examined the impact of a mixture of 22 contaminants detected in Inuit blood on the development and progression of NAFLD in obese JCR rats with or without co-exposure to10% ethanol. Hepatosteatosis was found in obese rat liver, which was worsened by exposure to 10% ethanol. NCM treatment increased the number of macrovesicular lipid droplets, total lipid contents, portion of mono- and polyunsaturated fatty acids in the liver. This was complemented by an increase in hepatic total cholesterol and cholesterol ester levels which was associated with changes in the expression of genes and proteins involved in lipid metabolism and transport. In addition, NCM treatment increased cytochrome P450 2E1 protein expression and decreased ubiquinone pool, and mitochondrial ATP synthase subunit ATP5A and Complex IV activity. Despite the changes in mitochondrial physiology, hepatic ATP levels were maintained high in NCM-treated versus control rats. This was due to a decrease in ATP utilization and an increase in creatine kinase activity. Collectively, our results suggest that NCM treatment decreases hepatic cholesterol export, possibly also increases cholesterol uptake from circulation, and promotes lipid accumulation and alters ATP homeostasis which exacerbates the existing hepatic steatosis in genetically obese JCR rats with or without co-exposure to ethanol.

Increased interest in measuring uranium isotope ratios in environmental samples (biological materials, soils, dust particles, water) has come from the necessity to assess the health impact of the use of depleted uranium (DU) based ammunitions during recent military conflicts (e.g., Gulf war, Kosovo) and from the need to identify nondeclared nuclear activities (nuclear safeguards). In this context, very important decisions can arise which have to be based on measurement data of nondisputable uncertainty. The present study describes the certification to 2.5% (k = 2) relative combined uncertainty of n(235U)/n(238U) at ultralow uranium levels (approximately 5-20 pg g(-1)) in human urine samples. After sample decomposition and matrix separation, the isotope ratios were measured by means of a single-detector magnetic sector-field inductively coupled plasma mass spectrometry instrument fitted with an ultrasonic nebulizer. Correction for mass discrimination effects was obtained by means of the certified isotopic reference material IRMM-184. The analytical procedure developed was validated in three complementary ways. First, all major sources of uncertainty were identified and propagated together following the ISO/GUM guidelines. Second, this quality was controlled with a matrix matching NUSIMEP-3 sample (approximately 0.06-0.7% difference from certified). Third, the instrumental part of the procedure was proven to be reproducible from the confirmation of the results obtained for three samples remeasured 7 months later (approximately 1.5% difference). The results obtained for 33 individuals indicated that none seemed to have been exposed to contamination by DU.

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