Sulfate-reducing prokaryotes (SRP) cause severe problems like microbial corrosion and reservoir souring in seawater-injected oil production systems. One strategy to control SRP activity is the addition of nitrate to the injection water. Production waters from two adjacent, hot (80°C) oil reservoirs, one with and one without nitrate treatment, were compared for prokaryotic community structure and activity of SRP. Bacterial and archaeal 16S rRNA gene analyses revealed higher prokaryotic abundance but lower diversity for the nitratetreated field. The 16S rRNA gene clone libraries from both fields were dominated by sequences affiliated with Firmicutes (Bacteria) and Thermococcales (Archaea). Potential heterotrophic nitrate reducers (Deferribacterales) were exclusively found at the nitrate-treated field, possibly stimulated by nitrate addition. Quantitative PCR of dsrAB genes revealed that archaeal SRP (Archaeoglobus) dominated the SRP communities, but with lower relative abundance at the nitrate-treated site. Bacterial SRP were found in only low abundance at both sites and were nearly exclusively affiliated with thermophilic genera (Desulfacinum and Desulfotomaculum). Despite the high abundance of archaeal SRP, no archaeal SRP activity was detected in [35 S]sulfate incubations at 80°C. Sulfate reduction was found at 60°C in samples from the untreated field and accompanied by the growth of thermophilic bacterial SRP in batch cultures. Samples from the nitrate-treated field generally lacked SRP activity. These results indicate that (i) Archaeoglobus can be a major player in hot oil reservoirs, and (ii) nitrate may act in souring control-not only by inhibiting SRP, but also by changing the overall community structure, including the stimulation of competitive nitrate reducers.During the process of secondary oil recovery in offshore oil fields, most often sulfate-rich seawater is injected into the reservoir to increase pressure and enhance recovery. The supply of large amounts of sulfate as an electron acceptor and the presence of oil organics and their degradation products as electron donors facilitate the enrichment and growth of sulfate-reducing prokaryotes (SRP) in the reservoir, as well as in piping and topside installations (51, 54). The activity of SRP causes severe economic problems due to the reactivity and toxicity of the produced hydrogen sulfide (H 2 S). In addition to microbiologically influenced corrosion and reservoir souring, the efficiency of oil production is decreased due to plugging by SRP biomass and precipitated metal sulfides (12,39). Besides the use of broadspectrum biocides or inhibitors for sulfate reduction, the addition of nitrate effectively decreased the net production of H 2 S in model column studies (15,20,38) and field trials (7, 53). The mechanisms by which nitrate addition might affect souring control are (i) the stimulation of heterotrophic nitrate-reducing bacteria (hNRB) that outcompete SRP for electron donors, (ii) the activity of nitrate-reducing, sulfide-oxidizing bacteria (NR-SOB...