Purpose Hexachlorocyclohexane (HCH) isomers (α-, β- and γ- (Lindane)) were recently included as new persistent organic pollutants (POPs) in the Stockholm Convention, and therefore, the legacy of HCH and Lindane production became a contemporary topic of global relevance. This article wants to briefly summarise the outcomes of the Stockholm Convention process and make an estimation of the amount of HCH waste generated and dumped in the former Lindane/HCH-producing countries. Results In a preliminary assessment, the countries and the respective amount of HCH residues stored and deposited from Lindane production are estimated. Between 4 and 7 million tonnes of wastes of toxic, persistent and bioaccumulative residues (largely consisting of alpha- (approx. 80%) and beta-HCH) are estimated to have been produced and discarded around the globe during 60 years of Lindane production. For approximately 1.9 million tonnes, information is available regarding deposition. Countries are: Austria, Brazil, China, Czech Republic, France, Germany, Hungary, India, Italy, Japan, Macedonia, Nigeria, Poland, Romania, Slovakia, South Africa, Spain, Switzerland, Turkey, The Netherlands, UK, USA, and former USSR. The paper highlights the environmental relevance of deposited HCH wastes and the related POPs' contaminated sites and provides suggestions for further steps to address the challenge of the legacy of HCH/Lindane production. Conclusion It can be expected that most locations where HCH waste was discarded/stockpiled are not secured and that critical environmental impacts are resulting from leaching and volatilisation. As parties to the Stockholm Convention are legally required to take action to stop further POPs pollution, identification and evaluation of such sites are necessary.

Vertical profiles of carbon monoxide (CO) and ozone retrieved from Tropospheric Emission Spectrometer have been analyzed during two super cyclone systems Mala and Sidr. Super cyclones Mala and Sidr traversed the Bay of Bengal (BOB) region on April 24-29, 2006 and November 12-16, 2007 respectively. The CO and ozone plume is observed as a strong enhancement of these pollutants in the upper troposphere over the BOB, indicating deep convective transport. Longitude-height cross-section of these pollutants shows vertical transport to the upper troposphere. CO mixing ratio ~90 ppb is observed near the 146-mb level during the cyclone Mala and near 316 mb during the cyclone Sidr. Ozone mixing ratio ~60-100 ppb is observed near the 316-mb level during both the cyclones. Analysis of National Centers for Environmental Prediction (NCEP) reanalysis vertical winds (omega) confirms vertical transport in the BOB.

Background, aim, and scope The Jiangsu section of the Yangtze River is the downstream of the whole river, serving as an important drinking water source. Persistent toxic substances (PTS), from the industries such as automobile, textile, chemical, and electronic production, are not listed in the National Standard yet and not monitored and controlled. However, pollution of PTS can threaten the environment and human health. In order to understand the pollution status of the PTS contamination and recommend future rationalization of countermeasure, the PTS including organochlorine pesticides (OCPs), polyaromatic hydrocarbons (PAHs), polychlorobiphenyls (PCBs), and phthalates (PAEs) were investigated. Materials and methods Samples were collected at 15 sites from five main stream sections of the Yangtze River in Jiangsu Province. PTS were extracted using solid phase extract method. The analysis of OCPs, PCBs was performed using GC/ECD and PAHs, PAEs was performed by GC/MS. Results and discussions The method detection limits are low and the recoveries are from 58.1% to 110.3%. The total concentrations of OCPs, PCBs, PAHs, and PAEs were 0.27∼2.15 ng l⁻¹, <0.21∼44.4 ng l⁻¹, 0.012∼3.576 μg l⁻¹ and 0.178∼1.474 μg l⁻¹, respectively. γ-HCH, PCB28, PCB101, phenanthrene, anthracene, di-n-butyl phthalate, diethyl phthalate, and di-(2-ethylhexyl) phthalate are the major detected PTS. The concentration of most of the PTS was below the environmental quality standards for surface water of China. Conclusions The pollution status of OCPs, PCBs, PAHs, and PAEs were analyzed. PTS contamination levels of the five main stream sections were relatively low.

INTRODUCTION: Acid orange 52 (AO52), extensively used in textile industries, was decolorized by Pseudomonas putida mt-2. AO52 azoreduction products such as N,N′-dimethyl-p-phenylenediamine (DMPD) and 4-aminobenzenesulfonic acid (4-ABS), were identified in the static degradation mixture. These amines were identified only in media of static incubation, which is consistent with their biotransformation under shaken incubation (aerobic conditions). MATERIALS AND METHODS: Tests with azo products were carried out, and whole cells were found able to easily degrade DMPD contrary to 4-ABS. However, this last could be attacked by cell extract, and an oxygen uptake was observed during the reaction. RESULTS: Degradation of DMPD by entire cells led to the formation of catechol. These results show that P. putida was able to decolorize AO52 and metabolize its derivative amines. In addition, the ability of tested compounds was evaluated in vitro to reduce human plasma butyrylcholinesterase (BuChE) activity. CONCLUSION: Azoreduction products seem to be responsible for BuChE inhibition activity observed in static biodegradation extract. However, toxicity of AO52 completely disappears after shaken incubation with P. putida, suggesting that bacterium has a catabolism which enables it to completely degrade AO52 and especially, to detoxify the dye mixture.

Background The impact of shipping emissions on urban agglomerations close to major ports and vessel routes is probably one of the lesser understood aspects of anthropogenic air pollution. Little research has been done providing a satisfactory comprehension of the relationship between primary pollutant emissions, secondary aerosols formation and resulting air quality. Materials and methods In this study, multi-year (2003-2007) ambient speciated PM₁₀ and PM₂.₅ data collected at four strategic sampling locations around the Bay of Algeciras (southern Spain), and positive matrix factorisation model were used to identify major PM sources with particular attention paid to the quantification of total shipping emissions. The impact of the emissions from both the harbour of Algeciras and vessel traffic at the Western entrance of Mediterranean Sea (Strait of Gibraltar) were quantified. Ambient levels of V, Ni, La and Ce were used as markers to estimate PM emitted by shipping. Results and discussion Shipping emissions were characterised by La/Ce ratios between 0.6 and 0.8 and V/Ni ratios around 3 for both PM₁₀ and PM₂.₅. In contrast, elevated La/Ce values (1-5) are attributable to emissions from refinery zeolitic fluid catalytic converter plant, and low average V/Ni values (around 1) result mainly from contamination from stainless steel plant emissions. The direct contribution from shipping in the Bay of Algeciras was estimated at 1.4-2.6 μg PM₁₀/m³ (3-7%) and 1.2-2.3 μg PM₂.₅/m³ (5-10%). The total contribution from shipping (primary emissions + secondary sulphate aerosol formation) reached 4.7 μg PM₁₀/m³ (13%) and 4.1 μg PM₂.₅/m³ (17%).

INTRODUCTION: A greenhouse experiment was conducted to determine if Cucurbita pepo ssp. pepo (pumpkin) root exudates could increase the uptake of polychlorinated biphenyls (PCBs) into plants. Contaminated soil was pre-treated with pumpkin root exudates by first growing pumpkins in the soil. Plants (pumpkins and weeds) were grown in the pre-treated (root exudate group) and non-treated (control group) contaminated soils. Seeds from five weed species collected from two contaminated sites were germinated in sufficient quantities (n ≥ 6) for three seedlings to be planted in two groups. DISCUSSION: Plants from both the control group and the root exudate group extracted a combined total of ∼1.2% PCBs from soil. Differences in root concentrations between groups were observed for Bidens cernua (beggar’s tick) and in total PCBs extracted into the roots for pumpkins. This is the first report of significant changes in the PCB phytoextraction ability of multiple plant species due to the presence of root exudates. In addition, slight differences were also observed for root and shoot concentrations and extractions by several other species, though these were not statistically different at α = 0.05. While the mechanism of phytoextraction is still unknown, this study indicates that the root exudates of C. pepo ssp. pepo can affect the uptake and transport of contaminants within specific plant species.

Background, aim, and scope A rapid increase in anthropogenic nitrogen inputs has a strong impact on terrestrial and aquatic ecosystems. We have estimated net anthropogenic nitrogen accumulation (NANA) as an index of nitrogen (N) pollution potential in the Beijing metropolitan region, China. Our research provides a basis for understanding the potential impact of anthropogenic N inputs on environmental problems, such as nation-wide water quality degradation under the current rapid urban expansion in modern China. Methods The NANA estimation is based on an inventory of atmospheric N deposition, N fertilizer use, consumption of human food and animal feed, N fixation, and riverine N import and export. We calculated N accumulation values for the years 1991, 1997, 2003, and 2007. Results and discussion The average NANA values for the urban and suburban areas from 1991 to 2007 were 24,038 and 13,090 kg N km⁻² year⁻¹, respectively. NANA is higher in eastern and southern areas than in northern and western areas, and higher in the urban area than in the suburban area. The overall average NANA in Beijing has a downward trend from 15,187 kg N km⁻² year⁻¹ in 1991 to 11,606 kg N km⁻² year⁻¹ in 2007, but is still two to five times as that of developed countries. N input from nitrogenous fertilizer is the largest source of NANA, accounting for 44.4% (6,764 kg N km⁻² year⁻¹) of the total N input, followed by atmospheric N deposition and N in human food and animal feed. NANA is closely related to land use, on average 23,140 kg N km⁻² year⁻¹ in densely populated developed land, 17,904 kg N km⁻² year⁻¹ in agricultural land, and 10,445 kg N km⁻² year⁻¹ in forest land. Human population density is the best single predictor of NANA.

Background and purpose Surfactant-assisted soil washing and photocatalysis are well-known remediation processes of environmental concern. The application of photocatalysis to treat soil washing extracts containing 4-methylphenol, 4-ethylphenol and 4-tert-butylphenol in the presence of nonionic (C₁₂E₈ and C₁₂E₂₃) and anionic (SDS) surfactants and some of their binary mixtures was investigated in this work by studying the pollutants degradation in the presence of TiO₂ dispersions irradiated with simulated solar light. Materials and methods Clean soil samples were spiked with the investigated alkylphenols. Aqueous solutions of the chosen surfactants were placed in contact for some hours with the spiked soil samples in a rotatory mixer. The pollutants recoveries were evaluated via HPLC analysis. Photocatalytic experiments were performed in solarbox on aqueous solutions and on aqueous surfactant solutions containing the pollutants. Results The pollutants removal from the soil was proven effective using the examined surfactant solutions. The photocatalytic treatment of the wastes was faster using Brij 35, but also SDS and C₁₂E₈-SDS mixtures can be applied. After 2-5 h the complete pollutants abatement was obtained, depending on the surfactant chosen and on the amount of TiO₂ employed. On the contrary, the treatment of wastes containing C₁₂E₈ was an extremely slow process. Conclusions The photocatalytic approach can be applied to remove the examined aromatic pollutants from the washing wastes, confirming the viable coupling between this advanced oxidation method and the surfactant-based soil remediation treatments. Surfactant adsorption onto TiO₂ and micelles concentration play a dominant role.

Background and aim Many rivers have to receive treated or untreated wastewater as the main water sources in the world, especially in the countries facing with water shortage. For instance, the Haihe and Huaihe River Basin, which are among areas facing crises for water resources in China, receive 33,400 million tons of wastewater per year. As the sediment has large capacity for sorbing hydrophobic organic pollutants such as polycyclic aromatic hydrocarbons (PAHs), it can act as a natural repository for the contaminants. This means pollutants can release into water phase again under some conditions, such as resuspension, sediment dredging, etc. The objective of this research was to study the trends of PAH release from sediments in rivers receiving much wastewater, such as Yongding New River (YD), Northsewer (NS), and Southsewer (SS) from Haihe River Basin. These rivers received most of the wastewater from Tianjin, China and merge into Bohai Bay finally. Methods Sediments (namely YD, NS, and SS) were collected from Yongding New River, Northsewer, and Southsewer, respectively. The physical and chemical properties of the sediments, including particle size distribution, total organic carbon (TOC) and black carbon (BC) contents, elemental compositions, organic functional groups analyzed from Fourier transformed infrared (FTIR), and nuclear magnetic resonance (NMR) spectra, were characterized. PAH desorption from the sediments was measured with the Tenax shaken slurry desorption method. Results The NS sediment had a greatly higher TOC and BC contents, while lower BC-to-TOC ratio than YD and SS sediments. NMR and FTIR analysis showed that aliphatic carbons were more abundant in NS sediment than SS sediment. The desorption experiments showed that PAHs desorbed more rapidly from YD and NS sediments than from SS sediment. PAH fraction desorbed after each interval during the experiment except 0.8 day was significantly correlated with PAH properties among all the three sediments. Discussion The higher BC-to-TOC ratio in SS sediment corresponded to slower desorption rate and less desorption extent of PAHs from SS sediment among the three sediments. This probably could be explained by the extremely strong sorption ability of BC. It also proved that the sequestration of PAHs in sediment was not simply the result of higher organic carbon content. Conclusions Considering the physical and chemical characterization of the sediments and PAH desorption properties comprehensively, BC-to-TOC ratio was a more important factor controlling the behavior of PAHs in sediments than absolute TOC or BC content.