Organochlorine pesticides (OCPs) and stable isotopes were measured in muscle from 4 bird and 5 fish species from the Ethiopian Rift Valley region where DDT is used for malaria control and vast agricultural activities are carried out. We investigated the bioaccumulation of OCPs such as DDTs, HCHs, chlordanes, and heptachlors between the species, and examined the potential risk posed by these compounds for bird species. Significant differences in contaminant profiles and levels were observed within the species. Levels of total OCPs ranged from 3.7 to 148.7 μg/g lipid in bird and 0.04 to 10.9 μg/g lipid in fish species. DDTs were the predominant contaminant, and a positive relationship between δ15N and ΣDDT concentrations was found. The main DDT metabolite, p,p′-DDE was the most abundant and significantly greater concentrations in bird species (up to 138.5 μg/g lipid), which could have deleterious effects on survival and/or reproduction of birds.

The spatial distribution of metal bioavailability (Ni, Cu, Zn, and Pb) was first evaluated within the waters of Daliao River watershed, using the diffusive gradient in thin films (DGT) and chemical equilibrium models. To assess potential risks associated with metal bioavailability, site-specific 95% protection levels (HC5), risk characterizations ratios (RCR) and ratios of DGT-labile/HC5 were derived, using species sensitivity distribution (SSD). The highest bioavailability values for metals were recorded in the main channel of the Daliao River, followed by the Taizi River. Dynamic concentrations predicted by WHAM 7.0 and NICA-Donnan for Cu and Zn agreed well with DGT results. The estuary of the Daliao River was found to have the highest risks related to Ni, Cu, and Zn. The number of sites at risk increased when considering the total toxicity of Ni, Cu, and Zn.

Perchlorate (ClO4−) interferes with uptake of iodide in humans. Emission inventories do not explain observed distributions. Ozone (O3) is implicated in the natural origin of ClO4−, and has increased since pre-industrial times. O3 produces ClO4−in vitro from Cl−, and plant tissues contain Cl− and redox reactions. We hypothesize that O3 exposure may induce plant synthesis of ClO4−. We exposed contrasting crop species to environmentally relevant O3 concentrations. In the absence of O3 exposure, species exhibited a large range of ClO4− accumulation but there was no relationship between leaf ClO4− and O3, whether expressed as exposure or cumulative flux (dose). Older, senescing leaves accumulated more ClO4− than younger leaves. O3 exposed vegetation is not a source of environmental ClO4−. There was evidence of enhanced ClO4− content in the soil surface at the highest O3 exposure, which could be a significant contributor to environmental ClO4−.

Constructed wetlands remove trace organic contaminants via synergistic processes involving plant biomass that include hydrolysis, volatilization, sorption, biodegradation, and photolysis. Wetland design conditions, such as hydraulic loading rates (HLRs) and carbon loading rates (CLRs), influence these processes. Contaminant of emerging concern (CEC) removal by wetland plants was investigated at varying HLRs and CLRs. Rate constants and parameters obtained from batch-scale studies were used in a mechanistic model to evaluate the effect of these two loading rates on CEC removal. CLR significantly influenced CEC removal when wetlands were operated at HLR >5 cm/d. High values of CLR increased removal of estradiol and carbamazepine but lowered that of testosterone and atrazine. Without increasing the cumulative HLR, operating two wetlands in series with varying CLRs could be a way to improve CEC removal.

Surface sediments and corals (Acropora sp. and Montipora sp.) from the coastline of Kenting were analyzed in 2009 and 2010 for content levels of polycyclic aromatic hydrocarbons (PAHs) using gas chromatography-mass spectrometry. The total PAH concentrations (t-PAH) in corasls (143–1715 ng g−1 dw) were significantly higher than in the ambient sediments (2–59 ng g−1 dw) indicating the bioaccumulation of PAHs in corals. The spatial and seasonal variation in PAH levels suggested that land-loaded contaminants may be the main source of PAHs in the Kenting coral reefs. Based on molecular indices, PAHs were substantially of petroleum origin. The major PAH components were phenanthrene, pyrene and fluorine, but PAH congeners in corals and sediments still have characteristic composition patterns which would be altered by the bio/accumulation mechanisms. Further study is essential to assess and understand the impacts of these chemicals on coral reefs.

Various sources supply PAHs that accumulate in soils. The methodology we developed provided an evaluation of the contribution of local sources (road traffic, local industries) versus remote sources (long range atmospheric transport, fallout and gaseous exchanges) to PAH stocks in two contrasting subcatchments (46–614 km²) of the Seine River basin (France). Soil samples (n = 336) were analysed to investigate the spatial pattern of soil contamination across the catchments and an original combination with radionuclide measurements provided new insights into the evolution of the contamination with depth. Relationships between PAH concentrations and the distance to the potential sources were modelled. Despite both subcatchments are mainly rural, roadside areas appeared to concentrate 20% of the contamination inside the catchment while a local industry was found to be responsible for up to 30% of the stocks. Those results have important implications for understanding and controlling PAH contamination in rural areas of early-industrialized regions.

Carbon nanotubes (CNT) are strong sorbents for organic micropollutants, but changing environmental conditions may alter the distribution and bioavailability of the sorbed substances. Therefore, we investigated the effect of green algae (Chlorella vulgaris) on sorption of a model pollutant (diuron, synonyms: 3-(3,4-Dichlorophenyl)-1,1-dimethylurea, DCMU) to CNT (multi-walled purified, industrial grade, pristine, and oxidized; reference material: Diesel soot). In absence of algae, diuron sorption to CNT was fast, strong, and nonlinear (Freundlich coefficients: 105.79–106.24 μg/kgCNT·(μg/L)−n and 0.62–0.70 for KF and n, respectively). Adding algae to equilibrated diuron-CNT mixtures led to 15–20% (median) diuron re-dissolution. The relatively high amorphous carbon content slowed down ad-/desorption to/from the high energy sorption sites for both industrial grade CNT and soot. The results suggest that diuron binds readily, but – particularly in presence of algae – partially reversibly to CNT, which is of relevance for environmental exposure and risk assessment.

Pharmaceutical compounds (PCs) are introduced into agricultural soils via irrigation with treated wastewater (TWW). Our data show that carbamazepine, lamotrigine, caffeine, metoprolol, sulfamethoxazole and sildenafil are persistent in soils when introduced via TWW. However, other PCs, namely diclofenac, ibuprofen, bezafibrate, gemfibrozil and naproxen were not detected in soils when introduced via TWW. This is likely due to rapid degradation as confirmed in our microcosm studies where they exhibited half-lives (t1/2) between 0.2–9.5 days when soils were spiked at 50 ng/g soil and between 3 and 68 days when soils were spiked at 5000 ng/g soil. The degradation rate and extent of PCs observed in microcosm studies were similar in soils that had been previously irrigated with TWW or fresh water. This suggests that pre-exposure of the soils to PCs via irrigation with TWW does not enhance their biodegradation. This suggests that PCs are probably degraded in soils via co-metabolism.

The traditional way to study Sources–Receptor Relationships (SRRs) of wet deposition is based on sensitivity simulation, which has weakness in dealing with the non-linear secondary formation pollutants (e.g. ozone and nitrate). An on-line source tracking method has been developed in the Nested Air Quality Prediction Modeling System (NAQPMS) coupled with cloud-process module for the first time. The new model can not only quantify the total volume of the sulfate, nitrate and ammonium wet deposition with more accuracy, but also trace these acidic species to their emitted precursors. Compared with previous studies, our result clearly shows: (1) East China and Central China, which are the two primary export regions, have 15–30% and 10% effect on wet deposition in other areas, respectively; (2) Besides the above two regions, the total acid deposition in Southwestern and Northeastern China have reached or exceeded the critical loads under their own environmental conditions.

We studied the bonding and release kinetics of Cd, Cu and Pb from different soils in the older metropolitan area of Copenhagen. Total Cd, Cu and Pb concentrations were elevated 5–27 times in the urban soils compared to an agricultural reference soil, with Cd and Pb in mainly mobilisable pools and Cu in strongly bound pools. The soils were subjected to accelerated leaching studies in Ca(NO3)2 or HNO3 solutions resulting in release up to 78, 18 and 15% of total Cd, Cu and Pb soil concentrations over a period of 15 weeks. The relative initial Cd and Pb release rates increased 10 fold when pH decreased 2 and 3 units, respectively, while increases in Cu release rates were only seen at pH below 4. The total leachable Cu and Pb pools were higher in urban soils compared the agricultural reference soil but not for Cd.