Are Chinese consumers at risk due to exposure to metals in crayfish? A bioaccessibility-adjusted probabilistic risk assessment

Freshwater crayfish, the world's third largest crustacean species, has been reported to accumulate high levels of metals, while the current knowledge of potential risk associated with crayfish consumption lags behind that of finfish. We provide the first estimate of human health risk associated with crayfish (Procambarus clarkii) consumption in China, the world's largest producer and consumer of crayfish. We performed Monte Carlo Simulation on a standard risk model parameterized with local data on metal concentrations, bioaccessibility (phi), crayfish consumption rate, and consumer body mass. Bioaccessibility of metals in crayfish was found to be variable (68-95%) and metal-specific, suggesting a potential influence of metal bioaccessibility on effective metal intake. However, sensitivity analysis suggested risk of metals via crayfish consumption was predominantly explained by consumption rate (explaining >92% of total risk estimate variability), rather than metals concentration, bioaccessibility, or body mass. Mean metal concentrations (As, Cd, Cu, Ni, Pb, Se and Zn) in surveyed crayfish samples from 12 provinces in China conformed to national safety standards. However, risk calculation of phi-modified hazard quotient (HQ) and hazard index (HI) suggested that crayfish metals may pose a health risk for very high rate consumers, with a HI of over 24 for the highest rate consumers. Additionally, the phi-modified increased lifetime risk (ILTR) for carcinogenic effects due to the presence of As was above the acceptable level (10(-5)) for both the median (ILTR = 2.5 x 10(-5)) and 90th percentile (ILTR = 1.8 x 10(-4)), highlighting the relatively high risk of As in crayfish. Our results suggest a need to consider crayfish when assessing human dietary exposure to metals and associated health risks, especially for high crayfish-consuming populations, such as in China, USA and Sweden.HZ by the National Natural Science Foundation of China (41273087). LN was supported by European Union Marie Curie Actions, Grant FP People 2010 “IRSES Electroacross” and BG by the SAGE-IGERT Fellowship (US National Science Foundation)

Recycled household ceramic waste in eco-efficient cement: a case study

The ceramic wastes can cause strong damage to the environment. In this article, the experimental study was concentrated on the pozzolanic activity of household ceramic waste and clay bricks waste. The possibility of the partial replacement of Portland cement blended with ceramic waste powder without further heating treatment in different ratios was analyzed. The ceramic waste powder was mixed in samples in various ratios. The evaluation of the ceramic waste powder was performed by grain-size analyses using Laser granulometry, XRD, XRF, Frattini test and strength activity index (SAI) method. The results indicate that the pozzolanic activity of household ceramic waste was higher than that of clay bricks waste. The 15% of HC powder addition could be a possible upper bound for an effective substitution and may also be very cost-efficient for industrial application.The authors acknowledge the National Natural Science Foundation of China: Grant 51578109, and Fundação para a Ciência e a Tecnologia (SFRH/BPD/22680/2005)

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Selected results of environmental chamber experiments carried out in the new large indoor environmental chamber at the University of California at Riverside (UCR) that are relevant to quantifying ozone impacts of volatile organic compounds (VOCs) are described. Issues and data needs for quantification of VOC reactivities towards ground-level ozone are described. The ability of the current SAPRC-99 chemical mechanism to simulate recent data from this chamber concerning the ozone formation from irradiations of an ambient reactive organic gas (ROG)- NOx mixture and several new aromatics experiments are discussed. It was found that the mechanism consistently underpredicts ozone formation in ambient surrogate- NOx experiments at low ROG/NOx ratios, and also underpredicts the effects of adding CO to aromatic- NOx irradiations. The two problems may be related and suggest problems with the formulation of current mechanisms for atmospheric reactions of aromatics. Background Many different types of volatile organic compounds (VOCs) are emitted into the atmosphere, where they can affect photochemical ozone formation and other measures of air quality. Because they can react in the atmospheres at different rates and with differen