In order to better understand air pollution in deve-loping regions, such as China, it is important to investigate the wet deposition behavior of atmospheric trace metals and its sources in the subtropical watershed. This paper studies the seasonal change of trace metal concentrations in precipitation and other potential sources in a typical subtropical watershed (Jiazhuhe watershed) located in the downstream of the Yangtze River of China. The results show that typical crustal elements (Al, Fe) and trace element (Zn) have high seasonal variation patterns and these elements have higher contents in precipitation as compared to other metals in Jiazhuhe watershed. In addition, there is no observed Pb in base flow in this study, and the concentration magnitudes of Al, Ba, Fe, Mn, Sr, and Zn in base flow are significantly higher than that of other metals. During different rainfall events, the dynamic export processes are also different for trace metals. The various trace metals dynamic export processes lead to an inconsistent mass first flush and a significant accumulative variance throughout the rainfall events. It is found that in this region, most of the trace metals in precipitation are from anthropogenic emission and marine aerosols brought by typhoon and monsoon.

This study investigated organic matter (OM) and nutrient removal efficiency of mixed algal species from slaughterhouse wastewater (SWW) by using photo-bioreactor. For this purpose, different dilution multiples of 10, 4, and 2 were applied to the SWW, and pure wastewater was finally used for algal cultivation. OM and nutrient removal performance in an algal photo-bioreactor were severely affected by the dilution ratio. After 7 days of cultivation, the highest removal percentages of total organic carbon (TOC), total nitrogen (TN), and total phosphorus (TP) were 89.6, 70.2, and 96.2 %, respectively. Furthermore, the changes in eukaryotic algae and cyanobacterial species in the algal photo-bioreactors were investigated using polymerase chain reaction (PCR) and denaturing gradient gel electrophoresis (DGGE) techniques. The results indicated that cyanobacterial species were more efficient than eukaryotic species in removing nutrients from the SWW. This study suggests that mixed algal photo-bioreactors could be used efficiently in the treatment of SWW.

In this study, miscible displacement experiment and batch sorption experiments were performed with sulfadimethoxine, dye tracer, Brilliant Blue FCF (BB) and a conservative tracer (bromide) to depict, analyse and interpret transport paths of sulfadimethoxine in undisturbed and disturbed soil columns. Batch sorption experiment revealed that sorption potential increased in the order: Brilliant Blue FCF > sulfadimethoxine > bromide. The horizontal spatial patterns of sulfadimethoxine and the tracers were analysed in each depth, and selective samples were taken in horizontal cross-section. Non-adsorbable and conservative tracer, bromide spread more widely into longitudinal and horizontal direction than sulfadimethoxine and Brilliant Blue FCF, since adsorption reduced transversal dispersion of the sulfadimethoxine and dye. In non-stained area, residual concentrations of sulfadimethoxine were relatively lower than in stained areas. Therefore, Brilliant Blue FCF distribution can be used to approximate sulfadimethoxine movement in soil. However, presence of preferential flow networks found in undisturbed soil cores can enhance mobility of sulfadimethoxine and the tracers, due to faster flow velocities and non-equilibrium adsorption. Our findings showed that other dye tracers may also be applicable to identify transport pathways of various organic contaminants, of which physico-chemical properties are similar to those of the dye tracers. Preferential flow should be considered for drinking water managements and transport modelling, since this allows faster pollutants transport from their sources, and create critical consequences for groundwater quality and solute transport modelling.

This paper reports the results of the first geomechanical laboratory experiments carried out on the polluted submarine clayey sediments of the Mar Piccolo in Taranto (South of Italy). The study had to face with extreme difficulties for the very soft consistency of the sediments and the contaminants. The mineralogy, composition and physical properties of the sediments were analysed, along with their compression and shearing behaviour. The investigation involved sediments up to about 20 m below the seafloor, along three vertical profiles in the most polluted area of the Mar Piccolo, facing the Italian Navy Arsenal. The experimental results were used to derive a preliminary geotechnical model of the site, necessary for the selection and design of the most sustainable in situ mitigation solutions. Moreover, the experimental data reveal that the clayey sediments of the most polluted top layer do not follow the classical geotechnical correlations for normally consolidated deposits. This seems to open interesting perspectives about the effects of pollutants on the geotechnical behaviour of the investigated sediments.

Polybrominated diphenyl ethers (PBDEs) were measured in air (TSP and PM₂.₅) and dust samples collected from 16 households and the corresponding workplaces of eight volunteer citizens in Shanghai, China. The PBDEs concentrations in the workplace air (mean: 281 ± 126 pg m⁻³) were over two times higher than those in the household (121 ± 44.0 pg m⁻³), while the mean levels of PBDEs in dust were 995 ± 547 and 544 ± 188 ng g⁻¹ for workplace and household, respectively. BDE209 was the most abundant congener in all samples. PBDEs appeared to be composed of mostly small particles. The C ₚₐᵣₜᵢcₗₑ/C dᵤₛₜ ratios of less brominated PBDEs in PM₂.₅ were higher than those in TSP, while the values were approximately constant for the more brominated PBDEs. A correlation analysis by network indicated different sources and behavior of the PBDE congeners. The results of a cluster analysis were displayed on a heat map that specified the source and abundance of each PBDE congener. The daily PBDE exposure via dust ingestion was the predominant part of the total intake and was more than 10 times higher than the intake via inhalation.

Diffusive gradients in thin films (DGT)-induced flux in sediments (DIFS) (DGT-DIFS) model for phosphorus (P) has been investigated to provide a numerical simulation of a dynamic system of the DGT–pore water–sediment in Dianchi Lake (China). Kinetic parameter—T C (33–56,060 s), distribution coefficient—K d (134.7–1536 cm³g⁻¹), and resupply parameter—R (0.189–0.743) are derived by DGT measurement, the sediment/pore water test, and the DIFS model. The changes of dissolved concentration in DGT diffusive layer and pore water and sorbed concentration in sediment, as well as the ratio of C DGT and the initial concentration in pore water (R) and mass accumulated by DGT resin (M) at the DGT–pore water–sediment interface (distance) of nine sampling sites during DGT deployment time (t) are derived through the DIFS simulation. Based on parameter and curves derived by the DIFS model, the P release-transfer character and mechanism in sediment microzone were revealed. Moreover, the DGT-DIFS parameters (R, T C , K ₋₁ , C DGT), sediment P pool, sediment properties (Al and Ca), and soluble reactive P (SRP) in overlying water can be used to assess “P eutrophication level” at different sampling sites with different types of “external P loading.” The DGT-DIFS model is a reliable tool to reveal the dynamic P release in sediment microzone and assess “internal P loading” in the plateau lake Dianchi.

We aimed at assessing the effects of four wetland plant species commonly used in constructed wetland systems: Typha, Phragmites, Iris and Juncus for removing ibuprofen (IBU) and iohexol (IOH) from spiked culture solution and exploring the mechanisms responsible for the removal. IBU was nearly completely removed by all plant species during the 24-day experiment, whereas the IOH removal varied between 13 and 80 %. Typha and Phragmites were the most efficient in removing IBU and IOH, respectively, with first-order removal rate constants of 0.38 and 0.06 day⁻¹, respectively. The pharmaceuticals were taken up by the roots and translocated to the aerial tissues. However, at the end of the experiment, plant accumulation constituted only up to 1.1 and 5.7 % of the amount of IBU and IOH spiked initially. The data suggest that the plants mainly function by facilitating pharmaceutical degradation in the rhizosphere through release of root exudates.

One technique applied to restore degraded or contaminated soils is to use amendments made of different types of waste materials, which in turn may contain metals such as Cu, Pb and Zn. For this reason, it is important to determine the capacity of the soil to retain these materials, and to compare the sorption capacity between an amended soil and another unamended soil. The aim of this study was to determine the mobility and availability of these metals in the soil after applying the amendment, and how it affected the soil’s sorption capacity. Sorption isotherms were compared with the empirical models of Langmuir and Freundlich to estimate the sorption capacity. The overall capacity of the soils to sorb Cu, Pb or Zn was evaluated as the slope Kr. The amendments used in this study were a mixture made of compost and biochar in different proportions (20, 40, 60, 100 %), which were applied to the mine tailing from a settling pond from a copper mine. The mine tailing that were amended with the mixture of compost and biochar had a higher sorption capacity than the mine tailing from the unamended pond, and their sorption isotherms had a greater affinity towards Cu, Pb and Zn than the mine tailing that was studied. Therefore, the results obtained show that adding a mixture of compost and biochar favours the retention of Cu, Pb and Zn in mine tailing.

Gas phase polycyclic aromatic hydrocarbons (PAHs) in Hexi Corridor, Northwest China were determined during heating and non-heating seasons, respectively, using passive air samplers. Polyurethane foam (PUF) disks were chosen as the sampling medium. Fifteen PAHs out of the 16 PAHs classified by the United States Environmental Protection Agency (U.S. EPA) were detected in this field sampling investigation. The atmospheric levels of sampled PAHs were higher at urban sites than that at rural sites among 14 sampling sites and increased during heating season. The highest concentration (11.34 ng m⁻³) was observed in Lanzhou during the heating season, the capital and largest industrial city of Gansu Province. PAH contamination in air was dominated by three aromatic ring congeners. Possible sources of PAHs were apportioned using PAH species ratios and the principle component analysis (PCA) combined with a multiple linear regression (MLR) method. Fossil fuel consumption was identified to be the predominant source of PAHs over Hexi Corridor, accounting for 43 % of the concentration of total (15) PAHs. Backward and forward trajectory and cluster analysis were also carried out to identify potential origins of PAHs monitored at several urban and rural sites. Lung cancer risk of local residents to gas phase PAHs via inhalation exposure throughout the province was found to be around a critical value of the lung cancer risk level at 10⁻⁶ recommended by the U.S. EPA risk assessment guideline.

The photodegradation of diethyl phthalate (DEP) by UV/H₂O₂ and UV/TiO₂ is studied. The DEP degradation kinetics and multiple crucial factors effecting the clearance of DEP are investigated, including initial DEP concentration ([DEP]₀), initial pH values (pH₀), UV light intensity, anions (Cl⁻, NO³⁻, SO₄ ²⁻, HCO₃ ⁻, and CO₃ ²⁻), cations (Mg²⁺, Ca²⁺, Mn²⁺, and Fe³⁺), and humic acid (HA). Total organic carbon (TOC) removal is tested by two treatments. And, cytotoxicity evolution of DEP degradation intermediates is detected. The relationship between molar ratio ([H₂O₂]/[DEP] or [TiO₂]/[DEP]) and degradation kinetic constant (K) is also studied. And, the cytotoxicity tests of DEP and its degradation intermediates in UV/H₂O₂ and UV/TiO₂ treatments are researched. The DEP removal efficiency of UV/H₂O₂ treatment is higher than UV/TiO₂ treatment. The DEP degradation fitted a pseudo-first-order kinetic pattern under experimental conditions. The K linearly related with molar ratio in UV/H₂O₂ treatment while nature exponential relationship is observed in the case of UV/TiO₂. However, K fitted corresponding trends better in H₂O₂ treatment than in TiO₂ treatment. The Cl⁻ is in favor of the DEP degradation in UV/H₂O₂ treatment; in contrast, it is disadvantageous to the DEP degradation in UV/TiO₂ treatment. Other anions are all disadvantageous to the DEP degradation in two treatments. Fe³⁺ promotes the degradation rates significantly. And, all other cations in question inhibit the degradation of DEP. HA hinders DEP degradation in two treatments. The intermediates of DEP degradation in UV/TiO₂ treatment are less toxic to biological cell than that in UV/H₂O₂ treatment.