ALBERT

Description: Mass balance studies in forested catchments in the northeastern USA show that S losses via streamwater SO42- exceed measured atmospheric S inputs. Possible sources of the excess S loss include underestimated dry deposition, mineralization of organic S in soils, desorption of soil sulphate, oxidation of recently formed sulphides and mineral weathering. Evaluating the relative contribution of these sources and processes to SO42- export is important to our understanding of S cycling as well as to policy makers in their evaluation of the efficacy of S emission controls. In order to evaluate the potential for mineral weathering contributions to SO42- export, we measured concentration and isotopic composition (δ34S and δ18O) of SO42- in stream water, and concentration and δ34S values of four S fractions in bedrock and soil parent material in catchments of varying geological composition. Geological substrates with low S concentrations were represented by catchments underlain by quartzite and granite, whereas geological substrates with high S concentrations were represented by catchments underlain by sulphidic slate, schist and metavolcanic rocks. Catchments with S-poor bedrock had stream-water SO42- concentrations 〈100 μeq L-1 and isotopic values consistent with those of atmospheric SO42- that had been cycled through the organic soil pool. Catchments with S-rich bedrock had stream-water SO42- concentrations ranging from 56 to 229 μeq L-1. Isotopic values deviated from those of SO42- in atmospheric deposition, clearly indicating a mineral weathering source in some cases, whereas in others spatial variability of mineral δ34S values precluded the isotopic detection of a weathering contribution. These results, along with evidence suggesting formation of secondary sulphate minerals in bedrock weathering rinds, indicate that mineral weathering may be an important source of S in the surface waters of some forested catchments in the northeastern USA. © 2004 John Wiley and Sons, Ltd.