The Tibetan Plateau is suggested to be an important indicator region to study the global long-range atmospheric transport of persistent organic pollutants. In this study, atmospheric polycyclic aromatic hydrocarbons (PAHs) were studied in Lhasa City in the Tibetan Plateau, China. Air samples in gas and particle phases were concurrently collected by a modified high-volume air sampler from 5 August 2008 to 13 July 2009. The concentration of ∑16PAHs ranged from 18 to 160 ng m(-3) (with a geometric mean of 68 ng m(-3)). The most abundant PAHs were phenanthrene and benzo(b)fluoranthene in gas and particle phases, respectively. Compared with other two similar studies in Beijing and Harbin, different temporal trends were found between gas and particle phases PAHs in Lhasa. The influences of meteorological parameters (ambient temperature and relative humidity) and air masses from China, India, Southeast Asia, and West Asia were the two important reasons for explaining the difference, which was confirmed by the 5-day backward trajectories. This is the first comprehensive study to provide the evidence for the different influences of long-range atmospheric transport on gas and particle phases PAHs pollution in the Tibetan Plateau.

Iron and arsenic have been found to coexist in a water environment and the fate of arsenite in the aquatic system is influenced by iron. Goethite is a form of iron hydroxide, which is commonly found in sediments. In previous studies, we have used iron complexes to degrade organic pollutants. Results have shown that some organic pollutants could be totally degraded by iron complexes and our work indicated that iron might cause conversion of arsenic when irradiated. This work attempts to investigate the conversion of arsenite [As(III)] using natural goethite, as the iron source, to quantify the effect of various factors on photooxidation. We also consider the possible mechanism for photooxidation of As(III) using a suspension of natural goethite. The As(III) concentration variation under illumination was compared with the one in the dark to quantify the contribution of light to As(III) oxidation to As(V) in goethite suspended solution. The experiments under N₂ and air atmosphere confirmed the participation of dissolved oxygen. The photooxidation efficiency of As(III) under different conditions was compared to determine the effect of different environmental factors such as pH value, goethite concentration, and humic acid concentration on the photooxidation reaction. In the solution containing 100 μg L⁻¹ arsenite and 0.1 g L⁻¹ suspended goethite at pH 3.0, nearly 80 % of As(III) was photooxidized after irradiation by a 250-W metal halogen lamp (λ ≥ 313 nm) after 6 h. The effects of initial pH and goethite concentration and humic acid concentration were all examined. The results show that the greatest efficiency of photooxidation of As(III) was at pH 3.0. The extent of photooxidation decreased with increasing goethite concentration and fell sharply in the presence of humic acid under the conditions in this work. Although about 80 % of As(III) was photooxidized after irradiation by a 250-W halogen lamp at pH 3.0 in the presence of goethite suspension, photooxidation was also affected by factors such as pH, concentration of goethite, and presence of humic acid. The scavenger experiments showed that the HO• radical and photogenerated hole are the predominant oxidants in this system responsible for 87.1 % oxidation of As(III), while HO ₂ • /O ₂ •⁻ is responsible for 12.9 % oxidation of As(III).

This paper presents the results of wet precipitation chemistry from September 2009 to August 2010 at a high-altitude forest site in the southeastern Tibetan Plateau (TP). The alkaline wet precipitation, with pH ranging from 6.25 to 9.27, was attributed to the neutralization of dust in the atmosphere. Wet deposition levels of major ions and trace elements were generally comparable with other alpine and remote sites around the world. However, the apparently greater contents/fluxes of trace elements (V, Co, Ni, Cu, Zn, and Cd), compared to those in central and southern TP and pristine sites of the world, reflected potential anthropogenic disturbances. The almost equal mole concentrations and perfect linear relationships of Na⁺and Cl⁻suggested significant sea-salts sources, and was confirmed by calculating diverse sources. Crust mineral dust was responsible for a minor fraction of the chemical components (less than 15 %) except Al and Fe, while most species (without Na⁺, Cl⁻, Mg²⁺, Al, and Fe) arose mainly from anthropogenic activities. High values of as-K⁺(anthropogenic sources potassium), as-SO₄²⁻, and as-NO₃⁻observed in winter and spring demonstrated the great effects of biomass burning and fossil fuel combustion in these seasons, which coincided with haze layer outburst in South Asia. Atmospheric circulation exerted significant influences on the chemical components in wet deposition. Marine air masses mainly originating from the Bay of Bengal provided a large number of sea salts to the chemical composition, while trace elements during summer monsoon seasons were greatly affected by industrial emissions from South Asia. The flux of wet deposition was 1.12 kg N ha⁻¹ year⁻¹for NH₄⁺–N and 0.29 kg N ha⁻¹ year⁻¹for NO₃⁻–N. The total atmospheric deposition of N was estimated to be 6.41 kg N ha⁻¹ year⁻¹, implying potential impacts on the alpine ecosystem in this region.

Three different combinations of treatment techniques, i.e. electrocoagulation combined with microfiltration (EMR), membrane bioreactor (MBR) and electrocoagulation integrated with membrane bioreactor (hybrid MBR, (HMBR)), were analysed and compared for the treatment of tannery wastewater operated for 7 days under the constant trans-membrane pressure of 5 kPa. HMBR was found to be most suitable in performance as well as fouling reduction, with 94 % of chemical oxygen demand (COD) removal, 100 % chromium removal and 8 % improvement in percentage reduction in permeate flux compared to MBR with only 90 % COD removal and 67 % chromium removal. The effect of mixed liquor suspended solids on fouling was also investigated and was found to be insignificant. EMR was capable of elevating the flux but was not as efficient as HMBR and MBR in COD removal. Fouling reduction by HMBR was further confirmed by SEM-EDX and particle size analysis.

A 2-year sampling campaign was conducted in three wastewater treatment plants of various sizes in the Rome area to assess the occurrence of nutrients and micropollutants among primary, secondary and digested sludge. The primary purpose was to evaluate the quality of different sludge types and their suitability for agricultural use. Primary sludge was consistently more polluted than secondary in terms of organic micropollutants, whereas heavy metals partitioned equally among the sludge types. In digested sludge, the heavy metal concentrations were always below limit values proposed for agricultural utilisation. In contrast, organic micropollutants concentrated during anaerobic digestion and affected the quality of the digested sludge. Secondary sludge resulted less polluted and richer in nitrogen and phosphorus (up to three times) than primary sludge and is hence more suitable for agricultural use. Separate processing of primary and secondary sludge might therefore be an innovative option for sludge management that could maximise the possibilities of agricultural use of secondary sludge and limit disposal problems only to primary sludge. In fact, primary sludge could be easily treated and disposed of by conventional processes including thickening, anaerobic digestion, centrifugation and incineration, whereas the difficult digestibility of secondary sludge could be improved by disintegration pre-treatment before stabilisation.

Six antibiotics, tetracyclines (TCs), and quinolones (QNs) in farmland soils from four coastal cities in Fujian Province of China were investigated. Oxytetracycline was most frequently detected, followed by enrofloxacin, ciprofloxacin, chlorotetracycline, ofloxacin, and tetracycline, with maximum concentrations of 613.2, 637.3, 237.3, 2668.9, 205.7, and 189.8 μg kg(-1), respectively. Samples from Putian City contained the highest maximum concentration of ∑TCs (3,064.2 μg kg(-1)), whereas those from Fuzhou City contained the highest maximum concentration of ∑QNs (897.8 μg kg(-1)). It is noteworthy that the ∑TCs and ∑QNs in 46.4 and 28.6 % of samples exceeded the ecotoxic effect trigger value (100 μg kg(-1)), respectively. The concentrations of these antibiotics and five tetracycline resistance genes in four soil plots at depth profiles were quantified thereafter. In most cases, both antibiotics and resistance genes decreased with the increase of depth. Some antibiotics can be detected at a depth of 60-80 cm where the abundance of tetO, tetM, and tetX reached up to 10(7) copies g(-1). Additionally, the sum of all tet genes (normalized to 16S rRNA genes) correlated with ∑TCs significantly (r = 0.676). Our results suggest that resistance determinants can migrate to deeper soil layers and would probably contaminate groundwater by vertical transport.

In this study, the effect of the biostimulation of the autochthonous microbial community on the depletion of polychlorinated biphenyls (PCBs) in historically contaminated sediments (6.260 ± 9.3 10⁻³ μg PCB/ g dry weight) has been observed. Biostimulation consisted of (1) the amendment of an electron donor to favor the dehalogenation of the high-chlorinated PCBs and (2) the vegetation of sediments with Sparganium sp. plants to promote the oxidation of the low-chlorinated PCBs by rhizodegradation. The effects of the treatments have been analyzed in terms of both PCB depletion and changes of the autochthonous bacterial community structure. The relative abundance of selected bacterial groups with reference to untreated sediments has been evaluated by quantitative real-time PCR. The amendment of acetate determined the enrichment of anaerobic dechlorinators like Dehalococcoides sp. Vegetation with Sparganium sp. plants determined the enrichment of either (3) the dechlorinators, Dehalococcoides and the Chloroflexi o-17/DF-1 strains or (4) the Acidobacteria, β-Proteobacteria, Actinobacteria, α-Proteobacteria, Bacteroidetes, and Firmicutes. The combination of the two biostimulation strategy determined the 91.5 % of abatement of the initial PCB content.

Provincial-level data for population, livestock, land use, economic growth, development of sewage systems, and wastewater treatment rates were used to construct a river nitrogen (N) export model in this paper. Despite uncertainties, our results indicated that river N export to coastal waters increased from 531 to 1,244 kg N km(-2) year(-1) in the Changjiang River basin, 107 to 223 kg N km(-2) year(-1) in the Huanghe River basin, and 412 to 1,219 kg N km(-2) year(-1) in the Zhujiang River basin from 1980 to 2010 as a result of rapid population and economic growth. Significant temporal changes in water N sources showed that as the percentage of runoff from croplands increased, contributions of natural system runoff and rural human and livestock excreta decreased in the three basins from 1980 to 2010. Moreover, the nonpoint source N decreased from 72 to 58 % in the Changjiang River basin, 80 to 67 % in the Huanghe River basin, and 69 to 51 % in the Zhujiang River basin, while the contributions of point sources increased greatly during the same period. Estimated results indicated that the N concentrations in the Changjiang, Huanghe, and Zhujiang rivers during 1980-2004 were higher than those in the St. Lawrence River in Canada and lower than those in the Thames, Donau, Rhine, Seine, and Han rivers during the same period. River N export will reduce by 58, 54, and 57 % for the Changjiang River, Huanghe River, and Zhujiang River in the control scenario in 2050 compared with the basic scenario.

The purpose of this study was to investigate ozone, variations, and its correlation with meteorological parameters at a remote location on the Mali Lošinj Island, which has been a tourist and health resort area in the northern Adriatic. The measured data are discussed in relation to the EU guidelines (Directive 2002/3/EC; Directive 2008/50/EC). In order to characterize ambient air with respect to ozone vegetation injury and photochemical pollution, we calculated accumulated dose over a threshold of 40 parts per billion index and two photochemical pollution indicators. The influence of local meteorological parameters on the measured ozone volume fractions was also investigated. We used the multivariate technique principal component analysis to trace correlations between measured ozone concentration and meteorological parameters.