Predicting the transfer of contaminants in soils is often hampered by lacking validation of mathematical models. Here, we applied Hydrus-2D software to three agricultural soils for simulating the 1900–2005 changes of zinc and lead concentration profiles derived from industrial atmospheric deposition, to validate the tested models with plausible assumptions on past metal inputs to reach the 2005 situation. The models were set with data from previous studies on the geochemical background, estimated temporal metal deposition, and the 2005 metal distributions. Different hypotheses of chemical reactions of metals with the soil solution were examined: 100% equilibrium or partial equilibrium, parameterized following kinetic chemical extractions. Finally, a two-site model with kinetic constant values adjusted at 1% of EDTA extraction parameters satisfactory predicted changes in metal concentration profiles for two arable soils. For a grassland soil however, this model showed limited applicability by ignoring the role of earthworm activity in metal incorporation.

PURPOSE: Persistent organic pollutants (POPs) are of global concern due to their ubiquitous presence and toxicity. The occurence of polychlorinated dibenzo-p-dioxins (PCDDs), -dibenzofurans (PCDFs), co-planar biphenyls (PCBs), hexachlorocyclohexanes (HCH), dichlorodiphenyltrichloroethanes (DDT), and organochlorine pesticides (OCPs) in forest soil collected from Taurus mountains may have adverse effects on the environment and health. The aim of the study was to investigate the outcome and distribution of POPs in the environment and the possible grasshopper effect along an altitude transect from sea level up to nearly 2,000 m a.s.l at a spatial distance of about 60 km in the southeastern Turkish Mediterranean Sea. METHODS: The samples were collected at a height of 121, 408, 981, 1,225, 1,373, 1,639, and 1,881 m above sea level from Taurus Mountains, Turkey. The results were confirmed using high-resolution gas chromatography–high-resolution mass spectrometry. RESULTS: The levels of the PCDD in forest soil from Taurus Mountains varied from nearly 4 to 12 pg g−1 dry weight (dw). PCDF concentrations ranged from 2 to 7 pg g−1 dw. Considerably high DDT levels detected in five stations indicated (3,223–24,564 pg g−1) its extensive local application or atmospheric transport. PCB levels were determined between 80 and 288 pg g−1 dw. HCH concentrations ranged from 141 to 1,513 pg g−1 dw. The other OCP was between 102 and 731 pg g−1. CONCLUSION: Although the use of POPs has been banned, our results show that they could still be found in Turkey. Their presence may be attributed to the degradation of pesticides which are newly banned and, as well as to the atmospheric migration and deposition. The lattitude of sampling sites, the chemical, and physical parameters of soil have observed no effect on the fate of POPs in the environment.

Bioaccumulation is essential for gaining insight into the impact of exposure to organic micropollutants in aquatic fauna. Data are currently available on the bioaccumulation of persistent organic pollutants, but there is very little documentation on the bioaccumulation of pharmaceuticals and personal care products (PPCPs). The bioconcentration of selected PPCPs was studied in marine mussels (Mytilus galloprovincialis). The selected PPCPs were two organic UV filters, i.e., 2-ethylhexyl-4-trimethoxycinnamate (EHMC) and octocrylene (OC), and two benzodiazepines (BZP), i.e., diazepam (DZP) and tetrazepam (TZP). Laboratory experiments were performed in which M. galloprovincialis was exposed to these compounds either directly from water, for the less lipophilic substances (BZP) or via spiked food for lipophilic UV filters. M. galloprovincialis uptook and eliminated BZP following first-order kinetics. The biological half-life (t ₁/₂) of TZP was 1.4 days, resulting in a bioconcentration factor of 64 and 99 mL g⁻¹ dry weight (dw), respectively, for 2.3 and 14.5 μg L⁻¹ of exposure, while the biological half-life (t ₁/₂) of DZP was 0.4 days, resulting in a bioconcentration factor of 51 mL g⁻¹ dw for 13.2 μg L⁻¹ of exposure. The uptake of UV filter was rapid in mussels, followed by elimination within 24 h. EHMC increased from 15 to 138 ng g⁻¹ dw in 1 h and decreased to 25 ng g⁻¹ after 24 h for 11.9 μg L⁻¹ exposure. OC reached 839 ng g⁻¹ dw after 1 h and decreased to 33 ng g⁻¹ after 24 h for 11.6 μg L⁻¹ exposure. However, EHMC and OC were slightly accumulated in 48 h, i.e., 38 and 60 ng g⁻¹ dw, respectively.

OBJECTIVE: Due to its high elevation, rare human activities and proximity to south Asia where industries are highly developed, it is required to investigate the fragile environment of the Tibetan Plateau. We are aiming to obtain the concentration level, source, spatial distribution, temporal variation and potential environmental risk of Tibetan soils. METHODS: A total of 128 surf ace soil samples were collected and analyzed f or V, Cr, Mn, Co, Ni, Cu, Zn, As, Cd and Pb, and an additional 111 samples were analyzed f or Hg and total organic carbon. Concentration comparisons coupled with multivariate statistics were used to analysis the sources of elements of soils. We also carried out Risk assessment on the soils. RESULTS: Concentrations of Hg, Cr, Ni, Cd and Pb are slightly higher than those of the late 1970s. Concentrations of Cr and Ni are higher than averaged world background values. Tibetan soils present a high natural As concentration level. DISCUSSION: Anthropogenic sources may partly contribute to the elevated Hg, Cd and Pb concentrations. Cr and Ni are mainly originated from soil parent materials. Soil elements in Anduo and Qamdo regions may threaten the health of local people. CONCLUSION: Heavy metal elements of Tibetan Plateau are mainly from the natural source. Arsenic present a high background level. Soil elements in Anduo and Qamdo regions may threaten the health of local people, which should be of concern to scientists and the government.

BACKGROUND: The photocatalytic degradation of pyrene under UV (125 W Hg-Arc, 10.4 mW/cm2) irradiation of TiO2 aqueous suspension has been found to be highly improved with the dissolved transition metal ions like Cu2+, Fe3+, Ag+, and Au3+, etc. As the reduction potential of these metals lies below the conduction band (CB) position (−0.1 eV) of TiO2, the photoexcited electron transfer occurs more readily and reduces electron–hole recombination rate. Therefore, it has a beneficial influence on the photocatalytic ability of TiO2 because of rapid Fermi energy equilibrium between the CB of TiO2 and its surface adsorbed metal ions. RESULTS AND DISCUSSION: The Fermi level is referred to as the electrochemical potential and plays an important role in the band theory of solids. When metal and semiconductor are in contact, electron migration from photoirradiated semiconductor to the deposited metal occurs at the interface until two Fermi levels equilibrate and enhanced the photocatalytic activity of semiconductor photocatalyst. Ni2+ having more negative reduction potential (−0.25 eV) than the CB of TiO2 imparts negligible co-catalytic activity to TiO2 photoreaction. It also revealed that loading of Au3+ ions displayed higher degradation rate of pyrene than Au photodeposition. Furthermore, when the amount of dissolved Fe+3 and Au3+ ions gradually increases from 0.1 to 2 wt.%, the pyrene photodecomposition rate also become faster.

Chaohu Lake, one of the most eutrophicated lakes in China, has been suffering from long-term outside pollution, urban sewage, river outflows, and agricultural runoff which expectedly have been the main contributors of hydrocarbons. However, the contributions from these various sources have not been specified. The present study is aimed at identifying the potential sources of hydrocarbons in surface sediment around the whole lake and assessing the relative contributions using principal components analysis–multiple linear regression (PCA-MLR). Sixty-one surface sediments covering the whole Chaohu Lake and three main estuaries of inflowing rivers were collected, dried, extracted, and analyzed for 27 normal alkanes (n-alkanes, from C12 to C38, defined Σ27AH) and unresolved complex mixture (UCM) by GC/MS. Diagnostic ratios and PCA-MLR were utilized to apportion their sources. The concentrations of Σ27AH and UCM ranged from 434 to 3,870 ng/g and 11.9 to 325 μg/g dry weight, respectively, for all samples. The concentrations of Σ27AH in western region and estuary of Nanfei River were slightly higher but without statistical significance than those from eastern region and estuaries of Yuxi River and Hangbu River. The concentration of UCM from western region was significantly higher than that obtained from eastern region. These results reflect the importance of input of urban runoff by Nanfei River and serious eutrophication in western region. Aliphatic hydrocarbons in Chaohu Lake were mainly derived from high plant wax with mixed sources of phytoplankton and petroleum. Weak microbial decomposition of n-alkanes would be expected to occur from the low ratios of isoprenoid hydrocarbons pristine (pri) and phytane (phy) to n-C17 and n-C18, respectively. Higher plant, fossil combustion, petroleum residue, and phytoplankton were proposed as the main origines of aliphatic hydrocarbons by PCA while the contributions of individual n-alkane homologues, pri and phy from the identified sources (31 % from higher plant, 30 % from fossil combustion, 26 % from petroleum, and 19 % from phytoplankton) were well predicted using MLR. The distribution profile and corresponding diagnostic ratios of normal alkanes show the promising potential as a useful proxy for estimating the source and loading of pollutants in Chaohu Lake.

The aim of this study was to establish the temporal trends and spatial distribution of Polycyclic Aromatic Hydrocarbons (PAHs) in Ria de Vigo by means of studying the PAH burden in wild mussels. The samples were collected in eight sites along the margins of the Ria de Vigo during November from 1998 to 2008 and Polycyclic Aromatic Hydrocarbon contents were determined using high performance liquid chromatography–fluorescence derivatization (HPLC–FLD). Quality of chemical analysis was guaranteed by participation in QUASIMEME intercalibration exercises carried out during the period of analysis. The concentrations for the sum of 13 PAHs were in the range 24–480 μg/kg dw, typical of an urban and industrialized area (50–500 μg/kg dw) except for a punctual input in La Guía in 1998 that led to a concentration above 1,000 μg/kg dw. In general, the sites in the outermost section of the estuary (ría) showed the lowest values, with an increasing gradient in the medium and inner parts of the ría. Temporal patterns show, in general, a downward trend. The relative proportion of 3 and 4 ring PAHs also varies with the site, the former being predominant in the outermost area and the latter in the medium and inner parts of the ría. This is consistently related with the sources and processes taking place in different areas of the estuary.

PURPOSE: When fossil fuels on the Earth are used up, which kind of green energy can be used to replace them? Do every bioenergy generation or crop food chain results in environmental pollution? These questions are major concerns in a world facing restricted supplies of energy and food as well as environmental pollutions. To alleviate these issues, option biogases are explored in this paper. MATERIALS AND METHODS: Two types of biogas generators were used for modifying the traditional crop food chain [viz. from atmospheric CO2 photosynthesis to crops, crop stem/husk biowastes (burnt in cropland or as home fuels), to livestock droppings (dumping away), pork and people foods, then to CO2], via turning the biowaste pollutants into green bioenergies. By analyzing the traditional food chain via observation method, the drawbacks of by-product biowastes were revealed. Also, the whole cycle chain was further analyzed to assess its “greenness,” using experimental data and other information, such as the material balance (e.g., the absorbed CO2, investment versus generated food, energy, and wastes). RESULTS AND DISCUSSION: The data show that by using the two types of biogas generators, clean renewable bioenergy, crop food, and livestock meat could be continuously produced without creating any waste to the world. The modification chain largely reduced CO2 greenhouse gas and had a low-cost investment. The raw materials for the gas generators were only the wastes of crop stems and livestock droppings. Thus, the recommended CO2 bioenergy cycle chain via the modification also greatly solved the environmental biowaste pollutions in the world. CONCLUSIONS: The described two type biogases effectively addressed the issues on energy, food, and environmental pollution. The green renewable bioenergy from the food cycle chain may be one of suitable alternatives to fossil and tree fuels for agricultural countries.

PURPOSE: This study had an objective to identify the most potent chromium-resistant bacteria isolated from tannery effluent and apply them for bioremediation of chromium in tannery effluents. METHODS: Two such strains (previously characterized and identified by us)—Enterobacter aerogenes (NCBI GenBank USA Accession no. GU265554) and Acinetobacter sp. PD 12 (NCBI GenBank USA Accession no. GU084179)—showed powerful chromium resistivity and bioremediation capabilities among many stains isolated from tannery waste. Parameters such as pH, concentration of hexavalent chromium or Cr (VI), and inoculum volume were varied to observe optimum bioconversion and bioaccumulation of Cr (VI) when the said strains were grown in M9 minimal salt media. E. aerogenes was used to remediate chromium from tannery effluents in a laboratory level experiment. RESULTS: Observation by Scanning Electron Microscope and chromium peak in Energy Dispersive X-ray Spectroscopic microanalysis revealed that E. aerogenes helped remediate a moderate amount of Cr (VI) (8–16 mg L−1) over a wide range of pH values at 35–37°C (within 26.05 h). High inoculum percentage of Acinetobacter sp. PD 12 also enabled bioremediation of 8–16 mg L−1 of Cr (VI) over a wide range of temperature (25–37°C), mainly at pH 7 (within 63.28 h). The experiment with real tannery effluent gave very encouraging results. CONCLUSION: The strain E. aerogenes can be used in bioremediation of Cr (VI) since it could work in actual environmental conditions with extraordinarily high capacity.

INTRODUCTION: A chemometric evaluation has been done to classify metal ions in soils and to determine whether or not the gastric and intestinal phases of a physiologically based extraction test bear any relation to any of the phases of the four-stage Community Bureau of Reference (BCR) extraction protocol. MATERIALS AND METHODS: Nine trace analytes (As, Ba, Cd, Cr, Cu, Mn, Ni, Pb and Zn) were determined in extracts obtained from the BCR sequential extraction procedure as well as from in vitro gastro-intestinal experiments. The results showed that high As, Pb, Zn and Cd concentrations were found in these soils. Principal component analysis (PCA) and linear discriminant analysis were used as classification techniques. Stepwise multiple linear regression analysis was applied to the data set to determine how the bioaccessibility of a metal is linked to the operationally defined fractions of metal speciation in soil. RESULTS AND DISCUSSION: This analysis showed that the metal concentrations in the intestinal and gastric extracts are mainly dependent on the concentrations found in BCR phases 1 and 2 for each metal ion except for Cr, which was mainly dependent on the concentrations found in BCR phase 3. From the chemometric technique of correlation analysis, it was concluded that the metals extracted using BCR phases 1 and 2 are more likely to be bioaccessible, i.e. are also extracted by gastric and intestinal digestion solutions. When the correlation and PCA results were interpreted together, it indicated that the bioaccessiblity of Zn, Pb, Mn and Cd were higher than As, Ba, Cr, Ni and Cu for these soils.