| Abstract: | To test whether synchrotron‐based spectromicroscopy can be used to identify spatial patterns of sulfur (S) and iron (Fe) speciation as well as relationships between the speciation of S and Fe in soil colloids or aggregates at the micrometre and sub‐micrometre level, an anoxically prepared dissected soil aggregate (size ～1 mm3) was analyzed by µ‐XANES at the K‐edges of S (2472 eV) and Fe (7112 eV). The experiment included (i) elemental mapping at the S K‐edge (S, Si, Al) and the Fe K‐edge (Fe, Si), (ii) acquisition of 300 µm × 300 µm images of the region of interest with X‐ray energies of 2474 eV (addressing reduced organic and inorganic S), 2483 eV (total S), 7121 eV (divalent Fe) and 7200 eV (total Fe), as well as (iii) acquisition of S and Fe µ‐XANES spectra at two different positions, where image analysis suggested the dominance of reduced and oxidized S and Fe, respectively. Image analysis revealed a heterogeneous distribution of total Si, S and Fe as well as of different S and Fe species in the aggregate. Microregions which were either enriched in reduced or in oxidized S and Fe could be identified. A microregion with a large contribution of oxidized S (sulfate, sulfonate) to total S contained exclusively Fe(III) oxyhydroxides (probably ferrihydrite) as S‐bearing phase, whereas another microregion with a large contribution of reduced organic S (thiol, organic disulfide) to total S contained a small amount of Fe(II)‐bearing silicate in addition to the dominating Fe(III) oxyhydroxides. Our results show that combined S and Fe µ‐XANES is a powerful tool for studying microscale spatial patterns of S and Fe speciation as well as microscale relationships between the speciation of S and Fe in soil aggregates. |
