A combination of sequential extraction with stable isotope ratio measurements of Se might offer new insights into biogeochemical processes governing Se turnover in soils. Therefore, we determined the Se partitioning among three operationally defined sequential extracts (0.1 mol L"' KjHPO^-KHjPO^ at pH 7,0.05 mol L"' NaOH, cone.HNOj) and the stable isotope ratios of total Se (^''^''^Se values) in 10 topsoils under 5 different land uses (alluvial grasslands, forests, house gardens, parks, and roadside grassland) from the city of Bayreuth (ca. 73,000 inhabitants) in Germany. Furthermore, we detetmined S and SO^^" concentrations and stable isotope ratios of total S (ä'^S values) to support our interpretation ofthe Se concentrations and isotope ratios because of the chemical similarity of Se and S. All topsoils had low total Se concentrations (0.09-0.52 mg kg~ ). The latgest conttibution to total Se was extracted with NaOH compdsing up to 42%,which is thought to be associated with organic matter and metal oxides. The 5 ' Se values of total Se in the topsoils were close to the bulk Earth composition with an average J82//65Ç value of -0.03 + SD 0.38%c suggesting that there was no or linle Se isotope fractionation in soil. We attribute the small isotope fractionation to the low bioavailability of Se as a consequence ofthe presence of Fe oxides (adsorbing the dominating Se(IV) forms strongly), organic matter, and SO^ (prevents biouptake ofthe Se(IV) forms) in the study soils. Small Se isotope fractionations of-0.59 to -0.35%o in mainly forest soils and of 0.26 to 0.45%o in mainly alluvial soils were presumably caused by soil/plant-recycling and Se contamination by river water, respectively In spite ofthe similarities in the assimilation of S and Se by organisms, the total S and Se isotope ratios in soil were not correlated. Our results demonstrate that Se in urban soils developed ftom Se-poor substrates is minimally cycled through the biosphere likely because of low bioavailability and competition with SO, 2-