Urban–rural differences in atmospheric mercury speciation

Measurements of gaseous elemental mercury (GEM), particulate mercury (Hg_p), and reactive gaseous mercury (RGM) were concurrently recorded at an urban site in Detroit and a rural site in Dexter, both in Michigan for the calendar year 2004. Their average concentrations (±standard deviation) for the urban area were 2.5 ± 1.4 ng m^?3, 18.1 ± 61.0 pg m^?3, and 15.5 ± 54.9 pg m^?3, respectively, while their rural counterparts were 1.6 ± 0.6 ng m^?3, 6.1 ± 5.5 pg m^?3, and 3.8 ± 6.6 pg m^?3, respectively. The medians of urban-to-rural ratios of Hg concentrations indicate approximately 1-fold, 2-fold, and 3-fold gradients between Detroit and Dexter for GEM, Hg_p, and RGM, respectively. The urban–rural differences in Hg also varied considerably on different temporal scales and with wind flow patterns, which was most evident in RGM. Our results show that while Hg at both sites was impacted by regional sources, meteorological conditions, and photochemical transformations, the extent of variations in the observed urban-to-rural gradients, particularly in RGM, cannot be fully accounted for by these processes. Both analyses of the annual data and case studies indicate that the more variable and episodic nature of Hg, particularly RGM, seen in Detroit compared with Dexter, was the result of direct impact from local anthropogenic sources.     

Survey of Laboratory Performance Analysis of Simulated Ambient S02 Bubbler Samples

The Quality Control Branch of the Quality Assurance and Environmental Monitoring Laboratory, National Environmental Research Center, Research Triangle Park, N. C, coordinated a nationwide interlaboratory study which surveyed the ability of participating laboratories to analyze simulated ambient sulfur dioxide samples. The purposes of the study were (1) to provide participating laboratories with a means for self evaluation of their performance, and (2) to begin to acquire information which indicates the quality of ambient SO₂ data being reported.

Sample vials of sodium sulfite in mannitol were distributed to 134 laboratories throughout the country that routinely analyze for atmospheric SO₂. No restrictions were placed on the method of analysis other than that the normal absorbing solution used with the analysis be a tetrachloromercurate II solution. Each sample set contained five separate vials. Each vial, when mixed properly with absorbing reagent, simulated a 24 hour bubbler sample. The range of concentrations in each set extended from approximately the lower detectable limit of the pararosaniline method to approximately the alert level as described in Federal Regulations.     

Reference conditions for rivers of the German Baltic Sea catchment: reconstructing nutrient regimes using the model MONERIS

We introduce an approach for establishing reference conditions (RC) for rivers of the German Baltic Sea catchment, based on predictive modelling. An extensive data set of statistics from the year 1880 was coupled with literature data, providing a comprehensive basis for the calculation of regional historical nutrient emissions into rivers, river nutrient concentrations, and nutrient loading into the sea. Four different scenarios were calculated: scenario 1 assumed RC following previously established criteria for lakes (Poikane et al. in Environ Manag 45(6):1286–1298, 2010), scenario 4 applied the nutrient emission conditions of 1880 (considering non-intensive land usage, the presence of tile drainage systems, sewer systems, and the human population from 1880), and scenarios 2 and 3 considered intermediate conditions. Our results showed that nutrient emissions from scenario 1 accounted for approximately one-tenth of the currently observed total nitrogen (TN) and total phosphorus (TP) emissions. The nutrient emissions calculated for 1880 (scenario 4) were found to be 47 % (TN) and 55 % (TP) higher than those calculated considering reference lake conditions (scenario 1). Our results suggest that RC nutrient concentrations in rivers in the German Baltic Sea catchment were clearly below 0.05 mg/l for TP and 1 mg/l for TN. This range is in accordance with historical and calculated pristine nutrient concentrations from other rivers in similar catchments.     

The conversion of chicken manure to biooil by fast pyrolysis II. Analysis of chicken manure, biooils, and char by curie-point pyrolysis-gas chromatography/mass spectrometry (Cp Py-GC/MS)

The initial chicken manure and the three fractions derived from it by fast pyrolysis, that is, the two biooils Fractions I and II as well as the residual char were analyzed by Curie-point pyrolysis-gas chromatography/mass spectrometry (Cp Py-GC/MS). The individual compounds identified were grouped into the following six compound classes: (a) N-heterocyclics; (b) substituted furans; (c) phenol and substituted phenols; (d) benzene and substituted benzenes; (e) carbocyclics; and (f) aliphatics. Of special interest were the relatively high concentrations of N-heterocyclics in biooil Fraction II which was obtained in the highest yield and had the highest calorific value. Prominent N-heterocyclics in biooil Fraction II were methyl-and ethyl-substituted pyrroles, pyridines, pyrimidine, pyrazines, and pteridine. Also noteworthy was the high abundance of aliphatics in biooil Fraction I and the char. The alkanes and alkenes in biooil Fraction I ranged from n-C7 to n-C18 and C7:1 to C18:1, respectively, and those in the char from n-C7 to n-C19 and C7:1 to C19:1, respectively. The N-heterocyclics in the two biooil Fractions came from the chicken manure, from proteinaceous materials during fast pyrolysis or were formed during the fast pyrolysis manure conversion by the Maillard reaction which involved the formation of N-heterocyclics by amino acids interacting with sugars.     

Arsenaufnahme von Wildpflanzen auf einem kampfstoffkontaminierten Rüstungsaltlastenstandort

The risk assessment of former ammunition factories, where chemical weapons consisting of diphenylarsenic compounds have been produced or stored is difficult because of the lack of data concerning bioavailability and metabolism of the residues of these sternutators. In order to estimate the contamination of fodder plants by typical pollutants of the former Heeresmunitionsanstalt Löcknitz, the total concentration of arsenic was determined in 186 samples of wild plants. The total arsenic concentration in plants of high feed value did not exceed 1 ppm, whereas 15% of the samples of plants of middle and little value in regard to animal fodder showed arsenic concentrations above 1ppm. The uptake of arsenic by wild plants, however, appears to be comparably low taken the high-grade contamination of the soil into account. A final toxicological evaluation of the risk potential is not yet possible because it requires the characterization of the anorganic and organic arsenic compounds in these plants.