In this study, the characteristics of organic phosphorus (Po) fractions in sediments of six lakes from the middle and lower reaches of Yangtze River region and Southwestern China Plateau, China were investigated using a soil Po fractionation scheme, and the relationships between Po, inorganic phosphorus (Pi) and pollution status were also discussed. The results show that the rank order of Po fractions was: residual Po > HCl-Po > fulvic acid-P > humic acid-P > NaHCO3-Po, with their average relative proportion 8.7:4.6:3.2:2.1:1.0. Po fractions, especially nonlabile Po, were significantly correlated with organic matter, Po and NaOH-Pi. Different distribution patterns of P fractions were observed in those two different regions. Po fractions in the heavily polluted sediments were higher than those in moderately and no polluted sediments, it is suggested that Po should be paid more attention in the lake eutrophication investigation. Organic phosphorus fractions in sediments from 6 different trophic Chinese lakes were characterized using an improved fractionation scheme.

Inorganic arsenic is a chronic exposure carcinogen. Analysis of UK baby rice revealed a median inorganic arsenic content (n = 17) of 0.11 mg/kg. By plotting inorganic arsenic against total arsenic, it was found that inorganic concentrations increased linearly up to 0.25 mg/kg total arsenic, then plateaued at 0.16 mg/kg at higher total arsenic concentrations. Inorganic arsenic intake by babies (4-12 months) was considered with respect to current dietary ingestion regulations. It was found that 35% of the baby rice samples analysed would be illegal for sale in China which has regulatory limit of 0.15 mg/kg inorganic arsenic. EU and US food regulations on arsenic are non-existent. When baby inorganic arsenic intake from rice was considered, median consumption (expressed as μg/kg/d) was higher than drinking water maximum exposures predicted for adults in these regions when water intake was expressed on a bodyweight basis. Median consumption of organic arsenic levels for UK babies from baby rice is above threshold considered safe.

This study determines spatial trends and congener patterns of 2378-substituted polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) in surficial sediments of Lakes Erie and Ontario. Sediments are enriched in 2378-PCDFs in Lake Ontario, and the PCDD/F concentrations increased from shallow near-shore sediments towards deep-water depositional zone sediments. In Lake Erie, sediments were dominated by octachlorodibenzo-p-dioxin, and the highest PCDD/F concentrations were observed in the western basin and the southern shoreline of the central basin with a decrease towards the eastern basin and the northern shoreline of the central basin. Principal components analysis revealed that chemical manufacture and disposal of chemical waste along the Niagara River has been a major PCDD/F source to Lake Ontario; while PCDD/Fs in Lake Erie are from multiple sources including industrial sources along the Detroit River, major tributaries along the southern shoreline of the lake, and atmospherically-derived material from the upper lakes and connecting channels. Lake-wide 2378-PCDD/F congener patterns are first reported in L. Erie and L. Ontario sediments.

Chemical extractions have been shown to measure the biodegradable fraction of aromatic contaminants in soil; however, there is little research on the chemical prediction of aliphatic hydrocarbon degradation. The aim of this study was to investigate the potential for cyclodextrin extractions to predict hexadecane biodegradation in soil. Soils were amended with 10 or 100 mg kg−1 of a model alkane n-hexadecane and 100 Bq g−1 14C-n-hexadecane. Correlations between the extents of mineralisation and extractions of the 14C-contaminant were determined. Solvent shake extractions and aqueous CaCl2 extractions were poor predictors of hexadecane bioaccessibility. However, the novel HP-α-CD shake extraction showed close correlation (r2 = 0.90, n = 36, p < 0.05) to the mineralisation data. This novel extraction technique has the potential to be used to assess the biodegradable aliphatic hydrocarbon fraction in contaminated soils. Cyclodextrin shake extractions have the potential to predict the bioaccessibility of aliphatic hydrocarbons in soil.

To clarify the groundwater–soil–crop relationship with respect to arsenic (As) contamination, As concentration was measured in tubewell (TW) water, surface soil from farmyards and paddy fields, and fresh taro (Colocasia esculenta) leaves from farmyards in the farming villages of Bangladesh. The As concentration in TW water from farmyards was at least four times higher than the Bangladesh drinking water standard, and the concentration in fresh taro leaves was equal to or higher than those reported previously for leafy vegetables in Bangladesh. As concentration of surface soils in both farmyards and paddy fields was positively correlated with that of the TW water. Further, the concentration in surface soil was positively correlated with levels in fresh taro leaves in the farmyard. This study, therefore, clarified the groundwater–soil–crop relationship in farmyards and the relationship between groundwater–soil in paddy fields to assess the extent of As contamination in Bangladeshi villages. By extracting arsenic contaminated groundwater from a well, surface soil surrounding the well and crops planted in the surface soil became contaminated with arsenic.

The evaluation of microbial availability of contaminants is of high importance for better reflecting the processes governing contaminant fate in soil and for establishing the risk associated with contaminated sites. A sub-critical water extraction technique was assessed for its potential to determine the microbially degradable fraction of [14C]phenanthrene-associated activity in two dissimilar soils at three different ageing times (14, 28 and 49 days). For the majority of determinations, no significant (p > 0.05) difference between sub-critical water-extracted 14C-activity at 160 °C and the fraction mineralized by catabolically active Pseudomonas sp. was observed. Collectively, the results suggested that the sub-critical water extraction technique was an appropriate technique for predicting the biodegradable fraction of phenanthrene-associated 14C-activity in dissimilar soils following increasing soil-contaminant contact time. Sub-critical water extraction reflects phenanthrene bioaccessibility in the soil.

Most available exposure–response relationships for assessing crop loss due to elevated ozone (O3) have been established using data from chamber and open-top chamber experiments, using a simulated constant O3 concentration exposure (square wave), which is not consistent with the diurnal variation of O3 concentration that occurs in nature. We investigated the response of oilseed rape (Brassica napus L.) to O3 as affected by two exposure regimes: one with a diurnal variation (CF100D) and another with a constant concentration (CF100). Although the two exposure regimes have the same mean O3 concentration and accumulated O3 concentration above 40 ppb (AOT40), our results show that O3 at CF100D reduced biomass and number of pods/plant more than O3 at CF100. Both O3 exposures resulted in larger seed weights/100 pods compared to CF. Numbers of seeds/100 pods were reduced by CF100, while numbers of seeds/100 pods in the CF100D chambers were comparable to those in CF. Our results suggest that chamber experiments that use a constant O3 exposure may underestimate O3 effects on biomass and yields. Diurnal variation of O3 concentration should be considered when designing O3 exposure experiment.

After flooding, iron reduction in riverine wetlands may cause the release of large quantities of phosphorus. As phosphorus is an important nutrient causing eutrophication in aquatic systems, it is important to have a tool to predict this potential release. In this study we examined the P release to the soil pore water in soil cores from floodplains in the Netherlands and from less anthropogenically influenced floodplains from Poland. During the inundation experiment, concentrations of P in the pore water rose to 2–90 times the initial concentrations. P release was not directly related to the geographic origin of the soils. An important predictor variable of P release was found in the ratio between the concentration of iron-bound P and amorphous iron. This ratio may provide a practical tool for the selection of new areas for wetland creation, and for impact assessment of plans for riverine wetland restoration and floodwater storage. Mobilisation of phosphorus in floodplain wetland soils can be predicted with easily measurable soil characteristics.

In the San Bernardino Mountains of southern California, ozone (O(3)) concentrations have been elevated since the 1950s with peaks reaching 600 ppb and summer seasonal averages >100 ppb in the 1970s. During that period increased mortality of ponderosa and Jeffrey pines occurred. Between the late 1970s and late1990s, O(3) concentrations decreased with peaks approximately 180 ppb and approximately 60 ppb seasonal averages. However, since the late 1990s concentrations have not changed. Monitoring during summers of 2002-2006 showed that O(3) concentrations (2-week averages) for individual years were much higher in western sites (58-69 ppb) than eastern sites (44-50 ppb). Potential O(3) phytotoxicity measured as various exposure indices was very high, reaching SUM00 - 173.5 ppmh, SUM60 - 112.7 ppmh, W126 - 98.3 ppmh, and AOT40 - 75 ppmh, representing the highest values reported for mountain areas in North America and Europe.