Dissimilatory NO 3؊ reduction in sediments is often measured in bulk incubations that destroy in situ gradients of controlling factors such as sulfide and oxygen. Additionally, the use of unnaturally high NO 3 ؊ concentrations yields potential rather than actual activities of dissimilatory NO 3 ؊ reduction. We developed a technique to determine the vertical distribution of the net rates of dissimilatory nitrate reduction to ammonium (DNRA) with minimal physical disturbance in intact sediment cores at millimeter-level resolution. This allows DNRA activity to be directly linked to the microenvironmental conditions in the layer of NO 3 ؊ consumption. The water column of the sediment core is amended with 15 NO 3 ؊ at the in situ 14 NO 3 ؊ concentration. A gel probe is deployed in the sediment and is retrieved after complete diffusive equilibration between the gel and the sediment pore water. The gel is then sliced and the NH 4 ؉ dissolved in the gel slices is chemically converted by hypobromite to N 2 in reaction vials. The isotopic composition of N 2 is determined by mass spectrometry. We used the combined gel probe and isotopic labeling technique with freshwater and marine sediment cores and with sterile quartz sand with artificial gradients of 15 NH 4 ؉ . The results were compared to the NH 4 ؉ microsensor profiles measured in freshwater sediment and quartz sand and to the N 2 O microsensor profiles measured in acetylene-amended sediments to trace denitrification.Nitrate accounts for the eutrophication of many humanaffected aquatic ecosystems (19,21). Sediment bacteria may mitigate NO 3 Ϫ pollution by denitrification and anaerobic ammonium oxidation (anammox), which produce N 2 (13, 18). However, inorganic nitrogen is retained in aquatic ecosystems when sediment bacteria reduce NO 3 Ϫ to NH 4 ϩ by dissimilatory nitrate reduction to ammonium (DNRA) (5,12,16,39). Hence, DNRA contributes to rather than counteracts eutrophication (23). DNRA may be the dominant pathway of dissimilatory NO 3 Ϫ reduction in sediments that are rich in electron donors, such as labile organic carbon and sulfide (4,8,17,38,55). High rates of DNRA are thus found in sediments affected by coastal aquaculture (8, 36) and settling algal blooms (16).DNRA, denitrification, and the chemical factors that control the partitioning between them (e.g., sulfide) should ideally be investigated in undisturbed sediments. The redox stratification of sediments involves vertical concentration gradients of pore water solutes. These gradients are often very steep, and their measurement requires high-resolution techniques, such as microsensors (26, 42) and gel probes (9, 54). If, for instance, the influence of sulfide on DNRA and denitrification is to be investigated, one wants to know exactly the sulfide concentration in the layers of DNRA and denitrification activity, as well as the flux of sulfide into these layers. This information can easily be obtained using H 2 S and pH microsensors (22,43). It is less trivial to determine the vertical distribution of DNRA...