In this study, the top-down NOx emissions estimated from satellite observations of NO2 vertical column densities over North Korea from 1996 to 2009 were analyzed. Also, a bottom-up NOx emission inventory from REAS 1.1 from 1980 to 2005 was analyzed with several statistics. REAS 1.1 was in good agreement with the top-down approach for both trend and amount. The characteristics of NOx emissions in North Korea were quite different from other developed countries including South Korea. In North Korea, emissions from industry sector was the highest followed by transportation sector in the 1980s. However, after 1990, the NOx emissions from other sector, mainly agriculture, became the 2nd highest. Also, no emission centers such as urban areas or industrial areas were distinctively observed. Finally, the monthly NOx emissions were high during the warm season.

The AQUATOX model considers the direct toxic effects of chemicals and their indirect effects through foodwebs. For this study, the AQUATOX model was applied to evaluating the ecological risk of Polybrominated diphenyl ethers (PBDEs) in a highly anthropogenically disturbed lake-Baiyangdian Lake. Calibration and validation results indicated that the model can adequately describe the dynamics of 18 biological populations. Sensitivity analysis results suggested that the model is highly sensitive to temperature limitation. PBDEs risk estimate results demonstrate that estimated risk for natural ecosystems cannot be fully explained by single species toxicity data alone. The AQUATOX model could provide a good basis in ascertaining ecological protection levels of “chemicals of concern” for aquatic ecosystems. Therefore, AQUATOX can potentially be used to provide necessary information corresponding to early warning and rapid forecasting of pollutant transport and fate in the management of chemicals that put aquatic ecosystems at risk.

The knowledge deficit of organic aerosol (OA) composition has been identified as the most important factor limiting our understanding of the atmospheric fate and implications of aerosol. The efforts to chemically characterize OA include the increasing utilization of nuclear magnetic resonance spectroscopy (NMR). Since 1998, the functional composition of different types, sizes and fractions of OA has been studied with one-dimensional, two-dimensional and solid state proton and carbon-13 NMR. This led to the use of functional group ratios to reconcile the most important sources of OA, including secondary organic aerosol and initial source apportionment using positive matrix factorization. Future research efforts may be directed towards the optimization of experimental parameters, detailed NMR experiments and analysis by pattern recognition methods to identify the chemical components, determination of the NMR fingerprints of OA sources and solid state NMR to study the content of OA as a whole.

We aimed to assess the dynamics of pore water concentrations of Cd, Co, Cu, Ni, Zn and their controlling factors (EH, pH, DOC, Fe, Mn, and SO42−) in a contaminated floodplain soil under different flood-dry-cycles. Two parallel undisturbed groundwater lysimeters (mean values presented) were used for long term (LT; 94 days) and short term (ST; 21 days) flood-dry-cycles. Reducing conditions under LT lead to low EH and pH, while DOC, Co, Fe, Mn, and Ni increased. Cadmium, Cu, Zn, and SO42− increased under oxidizing conditions during ST. Cobalt and Ni revealed a similar behavior which seem to governed by EH/pH, Mn, Fe, and DOC. Cadmium, Cu, and Zn reveal a similar fate; their dynamics were affected by EH/pH, DOC, and SO42−. Our findings suggest that a release of Cd, Cu, Co, Fe, Mn, Ni, and Zn under different flood-dry-cycles can assumed what might create potential environmental risks in using metal-enriched floodplain soils.

Sediment and polyethylene sampler-based estimates of polychlorinated dibenzo-p-dioxin/dibenzofuran (PCDD/F) concentrations in Newark Bay, New Jersey (USA) benthic biota were compared. Biota concentrations based on sediment were estimated using an organic carbon (OC)-water partitioning model and an OC and black carbon (BC)-water dual model. Biota concentrations based on polyethylene were estimated from samplers deployed in the Newark Bay water column and samplers immersed in a sediment/porewater slurry in the laboratory. Porewater samplers provided the best estimates of biota concentrations (within 3.1×), with best results achieved for deposit-feeders (within 1.6×). Polyethylene deployed in deep water also provided good estimates of biota concentrations (within 4×). By contrast, OC-water partitioning overestimated biota concentrations by up to 7×, while OC and BC combined underestimated biota concentrations by up to 13×. We recommend passive samplers such as polyethylene for estimating concentrations of hydrophobic organic contaminants in field biota given its simplicity and relatively lower uncertainty compared to sediment equilibrium partitioning.

The aim of this study was to estimate the bioavailability of essential (Zn, Cu) and non-essential metals (Cd, Pb) to the earthworm Lumbricus rubellus exposed to soils originating from a gradient of metal pollution in Southern Poland. Metal uptake and elimination kinetics were determined and related to soils properties. Experimental results were compared with tissue metal concentrations observed in earthworms from the studied transect. Cd and Pb were intensively accumulated by the earthworms, with very slow or no elimination. Their uptake rate constants, based on 0.01 M CaCl2-extractable concentrations in the soils, increased with soil pH. Internal concentrations of Cu and Zn were maintained by the earthworms at a stable level, suggesting efficient regulation of these metals by the animals. The estimated uptake and elimination kinetics parameters enabled fairly accurate prediction of metal concentrations reached within a life span of L. rubellus in nature.

Particle reactive organic contaminants in estuarine sediments can lead to various environmental problems affecting ecosystem and public health. In this study, the occurrence and homologous distribution pattern of quaternary ammonium compounds (QACs) in the surficial sediments collected from the Pearl River Estuary (PRE), China were examined along with polychlorinated biphenyls (PCBs) and polybrominated diphenylethers (PBDEs). The composition pattern of the QACs was found to be uniform in most of the sediments analyzed throughout the PRE, and the average composition pattern was identical to that determined in the sewage sludge from Guangzhou, the biggest city in the PRE. Dialkyldimethylammonium compounds, the most abundant type of QACs, positively correlated to the total concentrations of PCBs and PBDEs in most of the sediments with similar composition patterns. Therefore, the QACs are proposed as potential tracers to evaluate the transport of sewage-derived pollution in estuarine environments.

Phthalates strongly and adversely affect reproduction, development and liver function. We did a cumulative risk assessment for simultaneous exposure to nine phthalates using the hazard index (HI) and the levels of nine phthalates in 1200 foodstuff samples. DEHP (di-2-ethylhexyl phthalate) present the highest level (mean: 0.443 mg/kg) in 1200 samples, and the highest average daily dose (ADD) was found in DEHP, ΣDBP(i + n) (the sum of dibutyl phthalate [DBP] isomers [DnBP + DiBP]) posed the highest risk potential of all the phthalates. In seven phthalates, the 95th percentiles of the ADDs for ΣDBP(i + n) in 0–6-yr-old children accounted for 91% (79–107%) of the tolerable daily intake, and the 95th percentiles of the HIs for the anti-androgenic effects of five phthalates in 0–3-yr-old children and 4–6-yr-old girls were >1. We conclude that the health of younger Taiwanese may be adversely affected by overexposure of phthalate-contaminated foods.

Styrene sulfonate (SS) and polystyrene sulfonates (PSSs) were used as surrogates of natural organic matter to study the effect of molecular weight (from 206.2 to 70,000 Da) on their sorption by a multiwalled carbon nanotube (MWCNT) and an activated carbon (AC) and on their stabilization of MWCNT suspension. Results indicate that surface-diffusion through the liquid-sorbent boundary was the rate-controlling step of the kinetic sorption of both MWCNTs and AC, and surface-occupying and pore-filling mechanisms respectively dominated the thermodynamic sorption of MWCNTs and AC. Sorption rates and capacities of MWCNTs and AC in molecular concentration of SS and PSS decreased with increasing molecular weight. The PSSs but not SS facilitated the stabilization of MWCNT suspension because of the increased electrosteric repulsion. The PSSs with more monomers had greater capabilities to stabilize the MWCNT suspension, but the capabilities were comparable after being normalized by the total monomer number.