Copper and zinc concentrations in human hair and popular foodstuffs in China

<p>Concentrations of copper (Cu) and zinc (Zn) were determined in 383 human hair samples and in 445 food samples purchased in 11 Chinese cities. The concentrations of Cu were 7.91, 5.39, 2.27 and 2.20 mg kg⁻¹ and those of Zn were 47.2, 24.8, 52.8 and 30.2 mg kg⁻¹ in vegetables, cereals, meat and fish, respectively. The overall mean concentrations of hair Cu and Zn were 8.97 and 128 mg kg⁻¹, respectively. Hair Cu and Zn concentrations were higher in females than in males, especially in the 13–19 and 20–50 year age groups. Hair Cu concentration increased with increasing age and these changes occurred mainly in males. In contrast, 51–65 years old females had the lowest hair Zn concentrations. Residents of rural areas had similar hair Cu or Zn concentrations to people in urban areas. There were no significant correlations between hair concentration and food intake in terms of Cu and Zn among the cities. The results indicate that hair Cu and Zn concentrations and their changes with biological and environmental factors cannot be explained satisfactorily by the estimated food intakes in the cities sampled.</p

Molecular-Scale Investigation with ESI-FT-ICR-MS on Fractionation of Dissolved Organic Matter Induced by Adsorption on Iron Oxyhydroxides

Adsorption by minerals is a common geochemical process of dissolved organic matter (DOM) which may induce fractionation of DOM at the mineral-water interface. Here, we examine the molecular fractionation of DOM induced by adsorption onto three common iron oxyhydroxides using electrospray ionization coupled with Fourier-transform ion cyclotron resonance mass spectrometry (ESI-FT-ICR-MS). Ferrihydrite exhibited higher affinity to DOM and induced more pronounced molecular fractionation of DOM than did goethite or lepidocrocite. High molecular weight (>500 Da) compounds and compounds high in unsaturation or rich in oxygen including polycyclic aromatics, polyphenols and carboxylic compounds had higher affinity to iron oxyhydroxides and especially to ferrihydrite. Low molecular weight compounds and compounds low in unsaturation or containing few oxygenated groups (mainly alcohols and ethers) were preferentially maintained in solution. This study confirms that the double bond equivalence and the number of oxygen atoms are valuable parameters indicating the selective fractionation of DOM at mineral and water interfaces. The results of this study provide important information for further understanding the behavior of DOM in the natural environment

Toxicity effects of di-(2-ethylhexyl) phthalate to <i>Eisenia fetida</i> at enzyme, cellular and genetic levels

<div><p>Di-(2-ethylhexyl) phthalate (DEHP) is a dominant phthalic acid ester (PAE) that has aroused public concern due to its resistance to degradation and its toxicity as an endocrine-disrupting compound. Effects of different concentrations of DEHP on <i>Eisenia fetida</i> in spiked natural soil have been studied in the body of the earthworm by means of soil cultivation tests 7, 14, 21 and 28 days after exposure. The results indicated that, in general, superoxide dismutase (SOD) activity, malondialdehyde (MDA) content, metallothionein (MT) content, the expression of heat shock protein 70 (HSP 70) and all the tested geno-toxicity parameters are promoted as time elapses and with increasing concentration of DEHP. However, peroxidase (POD) activity, neutral red retention time (NRRT) and mitochondrial membrane potential difference values were found to decrease even at a low concentration of DEHP of 1 mg kg^-1 soil (<i>p</i><0.05). Clear toxic effects of DEHP on <i>E</i>. <i>fetida</i> have been generally recognized by means of the disturbance of antioxidant enzyme activity/content and critical proteins, cell membrane and organelle disorder and DNA damage estimated by length of tail, tail DNA ratio, and tail moment parameters. A concentration of DEHP of 3 mg kg^-1 may be recommended as a precaution against the potential risk of PAEs in soils and for indicating suitable threshold values for other soil animals and soil micro-organisms.</p></div

Dissolution and Microstructural Transformation of ZnO Nanoparticles under the Influence of Phosphate

The toxicity and fate of nanoparticles (NPs) have been reported to be highly dependent on the chemistry of the medium, and the effects of phosphate have tended to be ignored despite the wide existence of phosphate contamination in aqueous environments. In the present study the influence of phosphate on the dissolution and microstructural transformation of ZnO NPs was investigated. Phosphate at a low concentration rapidly and substantially reduced the release of Zn²⁺ into aqueous solution. Synchrotron X-ray absorption spectroscopy and X-ray diffraction analysis reveal that interaction between ZnO NPs and phosphate induced the transformation of ZnO into zinc phosphate. Transmission electronic microscopy observation shows that the morphology of the particles changed from structurally uniform nanosized spherical to anomalous and porous material containing mixed amorphous and crystalline phases of ZnO and zinc phosphate in the presence of phosphate. To our knowledge, this is the first study in which the detailed process of phosphate-induced speciation and microstructural transformation of ZnO NPs has been analyzed. In view of the wide existence of phosphate contamination in water and its strong metal-complexation capability, phosphate-induced transformations may play an important role in the behaviors, fate, and toxicity of many other metal-based nanomaterials in the environment

Phytoremediation of diphenylarsinic-acid-contaminated soil by <i>Pteris vittata</i> associated with <i>Phyllobacterium myrsinacearum</i> RC6b

<p>A pot experiment was conducted to explore the phytoremediation of a diphenylarsinic acid (DPAA)-spiked soil using <i>Pteris vittata</i> associated with exogenous <i>Phyllobacterium myrsinacearum</i> RC6b. Removal of DPAA from the soil, soil enzyme activities, and the functional diversity of the soil microbial community were evaluated. DPAA concentrations in soil treated with the fern or the bacterium were 35–47% lower than that in the control and were lowest in soil treated with <i>P. vittata</i> and <i>P. myrsinacearum</i> together. The presence of the bacterium added in the soil significantly increased the plant growth and DPAA accumulation. In addition, the activities of dehydrogenase and fluorescein diacetate hydrolysis and the average well-color development values increased by 41–91%, 37–78%, and 35–73%, respectively, in the treatments with <i>P. vittata</i> and/or <i>P. myrsinacearum</i> compared with the control, with the highest increase in the presence of <i>P. vittata</i> and <i>P. myrsinacearum</i> together. Both fern and bacterium alone greatly enhanced the removal of DPAA and the recovery of soil ecological function and these effects were further enhanced by <i>P. vittata</i> and <i>P. myrsinacearum</i> together. Our findings provide a new strategy for remediation of DPAA-contaminated soil by using a hyperaccumulator/microbial inoculant alternative to traditional physicochemical method or biological degradation.</p

Does phytoextraction with <i>Sedum plumbizincicola</i> increase cadmium leaching from polluted agricultural soil?

Sedum plumbizincicola is a cadmium (Cd) and zinc hyperaccumulator that can activate Cd by rhizosphere acidification. However, there is little understanding of the Cd leaching risk from polluted soil during phytoextraction process. Here, pot and column experiments were conducted to monitor soil Cd leaching characteristics under different rainfall simulation conditions during S. plumbizincicola phytoextraction. Soil Cd leaching increased significantly with increasing simulated rainfall intensity. Compared with normal rainfall (NR), weak rainfall (WR) resulted in a 34.3% decrease in Cd uptake by S. plumbizincicola and also led to a 68.7% decline in Cd leaching. In contrast, Cd leaching under heavy rainfall (HR) was 2.12 times that of NR in the presence of S. plumbizincicola. After two successive growing periods, phytoextraction resulted in a 53.5–66.4% decline in the amount of soil Cd leached compared with controls in which S. plumbizincicola was absent. Even compared with maize cropping as a control, S. plumbizincicola did not instigate a significant increase in Cd leaching. The contribution of Cd leaching loss to the decline in soil total Cd concentration was negligible after phytoextraction in the pot experiment. Overall, the results contribute to our understanding of soil Cd leaching risk by phytoextraction with S. plumbizincicola. Repeated phytoextraction by hyperaccumulator Sedum plumbizincicola is an important remediation technology to remove Cd from contaminated soils. At the same time, Sedum plumbizincicola can also activate soil Cd by rhizosphere acidification. However, studies on the leaching risk of soil activated Cd during the phytoextraction process are very few. This study looked at the effects of Sedum plumbizincicola growth on soil Cd leaching with the changes in rainfall simulation and plant type. Results showed that repeated phytoextraction with Sedum plumbizincicola did not increase Cd leaching from contaminated soil.</p

Correlation between seasonal CO₂ emission and carbon input.

<p>Carbon input was calculated from current-season aboveground biomass only (A); and calculated from straw return of the previous season and the aboveground biomass in the current season (B); the abbreviations of the treatment are shown in the footnotes in <a href="http://www.plosone.org/article/info:doi/10.1371/journal.pone.0080887#pone-0080887-g002" target="_blank">Fig. 2</a>.</p