Polycyclic aromatic hydrocarbon transport processes on the scale of a flood event in the rural watershed of Le Bebec, France

Transport processes of polycyclic aromatic hydrocarbons (PAHs) were investigated in a rural watershed in France, which led to new quantitative results on the scale of a flood event. For that purpose, principal components analysis (PCA) combined with signal decomposition of PAH Breakthrough curves were used. The results obtained by PCA enabled us to distinguish (i) the transport of low molecular weight PAHs in dissolved form and (ii) the transport of high molecular weight PAHs in particulate form. The intermediate molecular weight PAHs are distributed in these two clusters. The application of a signal decomposition method confirms the results of PCA and makes it possible to quantify the mass PAH resulting, respectively, from resuspension (13.3mg, i.e. 77% of the total mass) and from direct transfer (2.8mg=16% of the total mass). For the resuspension phase, desorption of PAH (38% of the total exported mass) could be also distinguished from sediment resuspension (39%).     

Sequential treatment via Trametes versicolor and UV/TiO2/Ru(x)Se(y) to reduce contaminants in waste water resulting from the bleaching process during paper production

An efficient sequential, biological and photocatalytic treatment to reduce the pollutant levels in wastewater due to the bleaching process during paper production is reported. For a biological pre-treatment, 800 ml of non-sterilized effluent was inoculated with Trametes versicolor immobilized in polyurethane foam, with 25 g l(-1) glucose, 6.75 mM CuSO(4), and 0.22 mM MnSO(4) added, and cultured at 25 degrees C with an air flow of 800 ml min(-1) for 8d. The fungus did not inhibit growth of the heterotropic populations of the effluent. After 4d of culture, the chemical oxygen demand (COD) reduction and colour removal (CR) were 82% and 80%, respectively, with laccase (LAC) and manganese peroxidase (MnP) activities of 345 U l(-1) and 78 U l(-1), respectively. The COD reduction and CR correlated positively (p<0.0001) with LAC and MnP activities. Chlorophenol removal was 99% of pentachlorophenol, 99% of 2,3,4,6-tetrachlorophenol (2,3,4,6-TCP), 98% of 3,4-dichlorophenol (3,4-DCP) and 77% of 4-chlorophenol (4-CP), while 2,4,5-trichlorophenol (2,4,5-TCP) increased to 0.2 mg l(-1). The pre-treated effluent was then exposed to a photocatalytic treatment. The treatment with photolysis resulted in 9% CR and 46% COD reduction, 42% CR and 60% COD reduction by photocatalysis, and 62% CR and 85% COD reduction by heterogeneous photocatalysis with the system TiO(2)/Ru(x)Se(y) (Fig. 4). With this treatment the bacterial and fungal populations also decreased by 5 logarithmic units with respect to the biological treatment alone (Fig. 5). The total sequential treatment resulted in a 92% CR (from 5800 UC), 97% COD reduction (from 59 g l(-1)) and 99% chlorophenol removal at 96 h and 20 min.     

Chemical and biological characteristics of streams in the Owabi watershed

In this investigation, concentrations of physico-chemical and bacteriological qualities of water samples from the major streams within the Owabi watershed in Kumasi, Ghana, were measured at five different locations. The streams were moderately soft and neutral, having a mean pH range of 7.08 ± 0.2 to 7.88 ± 0.6. Total dissolved solids, total suspended solids, grease and oil, alkalinity, and the major ion levels varied significantly at each sampling site. Nutrient levels were however low and did not show any clear variation at sample locations. The bacteriological quality of the water was poor, rendering it unsafe for domestic purposes without treatment. The poor bacteriological quality was due to direct contamination by animal and human wastes. The streams have an appreciable self-purification capacity which is stressed by persistent pollution overloads caused by expanding human activities within the catchment. Cluster analysis performed on the data to determine pollution patterns between the streams depicts that River Owabi was less polluted, Rivers Akyeampomene and Sukobri were moderately polluted, while River Pumpunase was highly polluted.     

Seasonal source influence on river mass flows of benzotriazoles

The anticorrosive agents 1H-benzotriazole (1H-BT), 4-methyl-1H-benzotriazole (4 Me-BT) and 5-methyl-1H-benzotriazole (5 Me-BT), which are usually added to dishwasher detergents, automotive antifreeze formulations and aircraft de-icing/anti-icing fluids (ADAFs), were measured in river water. Samples were collected from 15 sampling sites in the mainstream and selected tributaries of a medium-sized catchment area during summer and winter periods. The aim of this study was to assess a seasonal source influence on mass flows of benzotriazoles (BTs). The study area was representatively selected for an area with a possible influence of airport surface runoff. River discharge measurements were also performed. Moreover, BT concentrations were measured in an anti-icing and a de-icing fluid used at German airports as well as in several dishwasher detergents. The highest concentrations of all three compounds in river water were measured during the winter seasons. The maximum BT mass flows were calculated for all three substances in January when the mean monthly air temperature was the lowest; mass flows were the lowest in July when the mean monthly air temperature was the highest. A significant seasonal influence on BT mass flows in river water was observed for monitoring stations with a possible influence of airport surface runoff and for sampling locations where such an influence could be excluded. This indicates an input of BTs from other temperature-dependent applications, e.g. the use of antifreeze formulations in automotive windscreen wiper or cooling systems. 1H-BT was detected in two dishwasher tablets; 4 Me-BT and 5 Me-BT were not detected. BTs were measured in the anti-icing fluid with concentrations of 715 ng g(-1) (1H-BT), 1425 ng g(-1) (4 Me-BT) and 536 ng g(-1) (5 Me-BT); none of the BTs were detected in the de-icing fluid. Distribution patterns of BTs in ADAF and dishwasher detergents differed from those in river water.     

Correction to: Documenting lemming population change in the Arctic: Can we detect trends?

Ambio - In the original published article, some of the symbols in figure 1A were modified incorrectly during the typesetting and publication process. The correct version of the figure is provided...     

Characterization of endocrine disruptors from a complex matrix using estrogen receptor affinity columns and high performance liquid chromatography–high resolution mass spectrometry

Complex mixtures of contaminants with potential adverse effects on human health and wildlife are found in the environment and in the food chain. These mixtures include numerous anthropogenic compounds of various origins and structures, which may behave as endocrine disruptors. Mixture’s complexity is further enhanced by biotic and abiotic transformations. It is therefore necessary to develop new strategies allowing the identification of the structure of known, as well as unknown, nuclear receptor (NR) ligands present in complex matrices. We explored the possibility to use NR-based affinity columns to characterize the presence of bioactive molecules in environmental complex mixtures. Estrogen receptor α (ERα)-based affinity columns were used to trap and purify estrogenic substances present in surface sediment samples collected in a French river under mixed anthropogenic pressure. We combined biological, biochemical and analytical approaches to characterize the structure of ligands retained on columns and demonstrate the presence of known active molecules such as bisphenol A and octylphenol, but also of unexpected ERα ligands (n-butylparaben, hydroxyl-methyl-benzofuranone). High resolution mass spectrometry results demonstrate that ERα affinity columns can be used for the isolation, purification and identification of known as well as unknown estrogenic contaminants present in complex matrices.     

Using the chemical mass balance model to estimate VOC source contributions in newly built timber frame houses: a case study

Basing on the material emission data obtained in a test chamber, chemical mass balance (CMB) was used to assess the source apportionment of volatile organic compound (VOC) concentrations in three newly built timber frame houses. CMB has been proven to be able to discriminate the source contributions for two contrasted environmental conditions (with and without ventilation). The shutdown of the ventilation system caused an increase in the VOC concentrations due to the increased contribution of indoor surface materials like the door material and furniture explaining together over 65% of total VOCs. While the increase in formaldehyde concentration is mainly due to furniture (contribution of 70%), the increase in α-pinene concentration is almost exclusively attributable to the emission of door material (up to 84%). The apportionment of VOC source contributions appears as highly dependent on the position of source materials in the building (surface materials or internal materials) and the ventilation conditions explaining that the concentrations of compounds after the shutdown of ventilation system do not increase in equivalent proportion. Knowledge of indoor sources and its contributions in real conditions may help in the selection of materials and in the improvement of construction operations to reduce the indoor air pollution.