Tree canopies are believed to act as a sink of atmospheric ammonia (NH₃). However, few studies have compared the uptake efficiency of different tree species. This study assessed the uptake of ¹⁵N-labelled NH₃ at 5, 20, 50 and 100 ppbᵥ by leaves and twigs of potted silver birch, European beech, pedunculate oak and Scots pine saplings in June, August and September 2008. Additionally, foliar uptake of ¹³C-labelled carbon dioxide (¹³CO₂) and leaf stomatal characteristics were determined per species and treatment date and the relation with ¹⁵NH₃ uptake and estimated stomatal ¹⁵NH₃ uptake were assessed. Both ¹⁵NH₃ and ¹³CO₂ uptake were affected by tree species and treatment date, but only ¹⁵NH₃ uptake was influenced by the applied NH₃ concentration. Depending on the treatment date, ¹⁵NH₃ uptake by leaves and twigs was highest at 5 (September), 20 (June) or 50 (August) ppbᵥ. Birch, beech and oak leaves showed the highest uptake in August, while for pine needles this was in June and, except at 5 ppbᵥ in June, the ¹⁵NH₃ uptake was always higher for the deciduous species than for pine. For all species except beech ¹³CO₂ uptake was highest in August and on every treatment date the ¹³CO₂ uptake by leaves of deciduous species was significantly higher than by pine needles. Leaf characteristics and ¹³CO₂ uptake did not provide a strong explanation for the observed differences in ¹⁵NH₃ uptake. This study shows that on the short-term a high interspecific variability exists in NH₃ uptake, which depends on the time in the growing season.

In epidemiological studies, ultrafine particle (UFP) data from a single monitoring site are generally used as a measure of population exposure potentially resulting in exposure misclassification. From August 2009 to October 2010, 1-week campaigns were conducted during each season. The temporal and spatial variations of UFP number size distributions were investigated at 12 monitoring sites distributed across a 9 × 9 km urban area in Rochester, New York using a Fast Mobility Particle SizerTM spectrometer. The overall average number concentrations of 5.6- to 560-nm particles in summer, winter, spring, and fall were 9,025, 10,939, 4,955, and 14,485 cm−3, respectively. Coefficients of divergence and correlation coefficients were calculated between site pairs to assess the spatial heterogeneity in the particle number size distributions. Moderate spatial divergence and uniform temporal variation were found for the chosen sites. Elevated UFP number concentrations were observed near highways, off-road diesel engines, and residential wood combustion sources, indicating significant contributions to the UFP exposure of people living adjacent to these sources. Our results suggest that one stationary monitoring site may not represent the actual human UFP exposure over a whole urban area.

Studies were conducted to examine the effect of flue gas carbon dioxide (CO₂) on solubility and availability of different metals in fly ash of Powder River Basin (PRB) coal, Wyoming, USA. Initial fly ash (control) was alkaline and contains large amounts of water-soluble and exchangeable metals. Reaction of flue gas CO₂ with alkaline fly ash resulted in the formation of carbonates which minimized the solubility of metals. Results for metal fractionation studies also supported this fact. The present study also suggested that most of the water-soluble and exchangeable metals present in the control (untreated) fly ash samples decreased in the flue gas-treated samples. This may be due to the transfer of the above two forms to more resistant forms like carbonate bound (CBD), oxide bound (OXD), and residual (RS). Geochemical modeling (Visual MINTEQ) of water solubility data suggested that the saturation index (SI) values of dolomite (CaMg(CO₃)₂) and calcite (CaCO₃) were oversaturated, which has potential to mineralize atmospheric CO₂ and thereby reduce leaching of toxic metals from fly ash. Results from this study also showed that the reaction of flue gas CO₂ with alkaline fly ash not only control the solubility of toxic metals but also form carbonate minerals which have the potential to fix CO₂.

The historical trend of heavy metal pollution recorded in sediment cores from Lake Shinji, western Japan, was investigated to evaluate the contribution of increasing long-range transport of heavy metals from the Asian continent in recent years. The concentrations of Cd, Co, Cr, Cu, Ni, Pb, Sb, and Zn and lead isotope ratios were determined for sediment cores collected at two sites in the lake. Among the metals, Cd, Sb, and Zn showed markedly high concentrations since the 1970s. Moreover, a high Pb concentration and less radiogenic lead isotope ratios have been observed since the 1980s in the core from a site close to the mouth of a major river. Air masses from the Asian continent, including China, Russia, and South Korea, have less radiogenic lead isotope ratios than those from Japan. This suggests that the recent increase in Pb concentration in the sediment core is primarily due to the long-range transport of heavy metals from the Asian continent, followed by their deposition in the catchment area of the river. The concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of the sediment around 2000 were calculated on the basis of the metal concentrations in excess of those before 1940. They were then compared with the volume-weighted annual average concentration ratios of Pb/Cd, Pb/Sb, and Pb/Zn of rain samples collected on the shore of the lake for 1999–2001. The result showed that the ratios of the former to the latter are 1.0 for Cd, 0.69 for Sb, and 0.31 for Zn. Thus, it is likely that the long-range transport of Cd and Sb from the Asian continent also contributes significantly to the recent increase in the concentrations of these metals in the sediment core from Lake Shinji. For Zn, however, the contribution from the Asian continent was evaluated to be small, suggesting the importance of local sources such as effluent discharges.

The Loxahatchee National Wildlife Refuge (Refuge) developed throughout millennia as a system with waters low in nutrients. Today, the Refuge wetlands are impacted by inflows containing elevated nutrient concentrations originating from agricultural sources. Surface water samples were collected monthly at 48 marsh and five canal sites from June, 2004 through May, 2011 and analyzed water quality trends by sampling perimeter, transition, and the interior zones based on distance from the canal towards the Refuge interior. Nutrient, inorganic ion, and C concentrations generally decreased with distance from the canal to the Refuge interior. These water quality parameters also decreased from the canal to the Refuge interior, but less sharply. This finding suggests that there has been less canal water intrusion into the Refuge during the sampling period. The origin of the high Ca and Cl concentrations in canal water is most likely from intrusion of connate seawater into the canal. The reason for the improved water quality from June, 2004 to June 2011 can be attributed to an improved STA1-East performance since 2005. Additionally, canal water that originally by-passed treatment in STA1-East and STA1-West, and flowed into the L-7 canal through the S-6 pump, is now diverted farther south into STA2 for treatment.

This study investigated the formation of volatile carbonaceous disinfection by-products (DBPs) and nitrogenous DBPs from chlorination of oxytetracycline. Six DBPs were identified including chloroform (CF), 1,1-dichloroacetone, 1,1,1-trichloroacetone (TCP), dichloroacetonitrile (DCAN), trichloroacetonitrile, and trichloronitromethane. DBP yields varied with different reaction conditions, including chlorine concentration, reacting time, pH, and bromide concentration. The highest DBP yields were found at Cl₂/C mass ratio and reaction time of 5 and 3 days, respectively. The solution pH had significant influence on CF, DCAN, and 1,1,1-TCP formation. The concentration of CF increased with the increase of pH, while DCAN and 1,1,1-TCP yields were high at acidic pH and decreased greatly under alkaline conditions. In the presence of bromide, the DBP composition shifted to multiple bromide compounds, including bromodichloromethane, dibromochloromethane, bromoform, bromochloroacetonitrile, and dibromoacetonitrile.

Crosslinking carboxymethyl starch (CCMS) powder of degree of substitution (DS) 0.43–0.59 was prepared by the process of two steps of alkali addition synthesis. The technique of powder coupling with ultrafiltration was used to absorb Cu2+, Zn2+, Ni2+, Pb2+, and Cd2+ from aqueous solutions. FTIR was used to demonstrate the successfully grafting of carboxymethyl groups, and the technique of microwave plasma torch atomic emission spectrometer was applied in rapid determination of the aforementioned heavy metals ions. The results revealed that the removal sequence of heavy metal ions followed the order of Pb2+>Cu2+>Cd2+>Zn2+>Ni2+. By assistant of diethylene triamine penlaacetic acid, the quaternary system of Pb2+/Ni 2+/Cd2+/Cu2+ mixture solution could have the ideal separation. Besides, the influence of pH, ζ potential, DS value, and membranes molecular weight cut-off on removal of 20 mg L−1 Pb2+ or Ni2+ was also investigated.

The present study evaluated the short-term toxicity of seven selected pesticides: four insecticides (chlorpyrifos, dieldrin, diazinon and pirimiphos-methyl) and three herbicides (diuron, alachlor and atrazine). With this aim, a standard toxicity test with the highly sensitive early life stages (ELS) of a marine fish was used. The turbot, Psetta maxima, is abundant in shallow estuarine and costal habitats and is currently the most commonly cultivated fish species in Galicia, NW Spain. According to the turbot ELS test results, chlorpyrifos was the most toxic pesticide tested for both embryos and larvae and was followed in order of decreasing toxicity by dieldrin, pirimiphos-methyl, diazinon, alachlor, atrazine and diuron. Larvae were more sensitive than embryos to the seven pesticides. The median lethal concentrations of the selected pesticides during a 48- and a 96-h exposure for turbot embryos and larvae were, respectively (in micrograms per litre): chlorpyrifos, 116.6 and 94.65; dieldrin, 146 and 97; pirimiphos-methyl, 560 and 452; diazinon, 1,837 and 1,230; alachlor, 2,177 and 2,233; diuron, 10,076 and 7,826; and atrazine, 11,873 and 9,957. According to their acute toxicity, the insecticides were more toxic than the herbicides. Furthermore, all insecticides and herbicides appear to be teratogenic to turbot ELS.

The impact of thermal pollution of leachate from a post-coal mine heap on three macrophyte species: Phragmites australis, Typha latifolia, and Scirpus sylvaticus was examined over the entire vegetation season. Hydrological measurements showed that the temperature of the leachate was ca 50 °C at the site of leachate inflow and decreased to ca 15 °C at the end of discharge canal. The annual temperature and conductivity of leachate from the two control sites, a polluted water stream in the vicinity of the waste tip and an unpolluted stream, differ significantly. However, only the temperature explained the differences in plant traits. In April, and in some cases in May, plants in the leachate were significantly higher than in those on the control sites in terms of biomass and plant height. Thermal pollution caused a phenological shift in all species and also caused Scirpus plants to die out more quickly. Temperature also affected the proportion flowering vs. vegetative individuals, e.g., none of Scirpus plants started to bloom.

Principal component analysis has been used as a tool for the detection of potentially outlying observations in multivariate data sets of polycyclic aromatic hydrocarbon concentrations (PAHs) in ambient air. The outlier statistic developed is the vector distance of each observation at a given site from the origin of principal component space. It is shown that the success of this technique relies on the usually very strong correlation of concentrations of different PAHs in ambient air, such that any deviation from this correlation is noteworthy. Indeed, it is so strong that the first principal component has been omitted from the technique since it is related mostly to absolute concentration. The method has been successful in detecting observations with unusually high concentrations of one or more PAHs. Moreover, it has been possible to identify periods where the UK pollution climate was abnormal during periods of extreme weather. Advice and guidance for the practical use of the technique is also given.