Persulfate oxidation was validated as a method to predict
polycyclic aromatic hydrocarbon (PAH) bioavailability in
soils and sediments. It was demonstrated for 14 field
contaminated soils and sediments that residual PAH
concentrations after a short (3 h) persulfate oxidation
correspond well to residual PAH concentrations after 21
days of biodegradation. Persulfate oxidation of samples that
had first been subjected to biodegradation yielded only
limited additional PAH oxidation. This implies that oxidation
and biodegradation removed approximately the same
PAH fraction. Persulfate oxidation thus provides a good
and rapid method for the prediction of PAH bioavailability.
Thermogravimetric analysis of oxidized and untreated
samples showed that persulfate oxidation primarily affected
expanded organic matter. The results indicate that this
expanded organic matter contained mainly readily bioavailable
PAHs.
After dredged sediments have settled in a temporary upland disposal site, ripening starts, which turns waterlogged sediment into aerated soil. Aerobic biological mineralization of organic matter (OM) and chemical oxidation of reduced sulfur compounds are the major biochemical ripening processes. Quantitative data describing these processes are scarce. Therefore, aerobic oxidation and mineralization of five previously anaerobic dredged sediments were studied during a 160-d laboratory incubation experiment at 30 degrees C. A double exponential decay model could adequately describe sulfur oxidation and OM mineralization kinetics. During the first 7 d of incubation, 23 to 80% of the total sulfur was oxidized, after which no further sulfur oxidation was observed. Oxygen used for sulfur oxidation amounted up to 95% of the total oxygen uptake in the first 7 d and up to 45% of the oxygen uptake during the entire incubation period. Mineralization rates of the rapidly mineralizable OM fractions that degraded during the first 14 to 28 d of incubation were 10(2) to 10(3) times higher than the mineralization rates of the slowly mineralizable OM during the remaining period. First-order mineralization rates of the slowly mineralizable OM were 0.22 x 10(-3) to 0.54 x 10(-3) d(-1) and can be compared with those of terrestrial soils. Yields of biomass on substrate ranged from 0.08 to 0.45 g C(biomass)/g C(OM) and appeared to be higher for rapidly mineralizing OM than for slowly mineralizing OM. The results of this study can be used to optimize conditions during temporary disposal of sediments, to estimate the potential decrease in OM, and for future studies on the possible link between OM mineralization and degradation of hydrophobic organic contaminants.
AquaTerra is one of the first environmental projects within the 6th Framework program by the European Commission. It began in June 2004 with a multidisciplinary team of 45 partner organizations from 13 EU countries, Switzerland, Serbia, Romania and Montenegro. Results from sampling and modeling in 4 large river basins (Ebro, Danube, Elbe and Meuse) and one catchment of the Brévilles Spring in France led to new evaluations of diffuse and hotspot input of persistent organic and metal pollutants including dynamics of pesticides and polycyclic aromatic hydrocarbons, as well as metal turnover and accumulation. While degradation of selected organic compounds could be demonstrated under controlled conditions in the laboratory, turnover of most persistent pollutants in the field seems to range from decades to centuries. First investigations of long-term cumulative and degradation effects, particularly in the context of climate change, have shown that it is also necessary to consider the predictions of more than one climate model when trying to assess future impacts. This is largely controlled by uncertainties in climate model responses. It is becoming evident, however, that changes to the climate will have important impacts on the diffusion and degradation of pollutants in space and time that are just at the start of their exploration. contaminants / organic / inorganic / European river basins / climate change / sorption / biodegradation / soil / sediment / ground-and surface water / heavy metals / review / pesticides / atrazine / isoproturon / alkyphenol / acetochlor / chlortoluron / organochlorine / Br diphenyl ethers / drugs / TOF mass spectrometry / 87Sr * Corresponding author: johannes.barth@uni-tuebingen.de 2 J.A.C. Barth et al.
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