Previous studies have demonstrated the potential for removal of U(VI) from solution via precipitation of U(VI)-bearing calcium-phosphate (Ca-P) minerals coupled to microbial hydrolysis of glycerol phosphate compounds. We evaluated this process in circumneutral-pH groundwater from Area 2 of the U.S. Department of Energy Field Research Center at Oak Ridge National Laboratory. Area 2 groundwater contains high concentrations of dissolved calcium (ca. 4 mM), and thus, release of phosphate during glycerol phosphate metabolism has the potential to create conditions favorable for U(VI) sequestration in Ca-P minerals. Microbial enumeration and isolation studies verified the presence of aerobic and nitrate-reducing glycerol 3-phosphate (G3P)-metabolizing microorganisms in Area 2 sediments. Coprecipitation of U(VI) with Ca-P minerals coupled to microbial G3P hydrolysis was demonstrated in artificial groundwater under aerobic and nitratereducing conditions. Transmission electron microscopy analysis and mineral-washing experiments demonstrated that U(VI) was incorporated into the structure of the insoluble Ca-P mineral hydroxyapatite [Ca 5 (PO 4 ) 3 OH]. Our results support the idea that U(VI) can be effectively removed from solution in contaminated aquifers through stimulation of microbial organophosphate metabolism.Reductive precipitation of U(VI) through stimulation of anaerobic, dissimilatory metal-reducing microbial activity is a demonstrated method for in situ immobilization of uranium in subsurface environments (3,41). This is an attractive approach for aquifers that are naturally low in dissolved O 2 and NO 3 Ϫ , e.g., the uranium-contaminated aquifer adjacent to the Colorado River in Rifle, CO (3). Alternative uranium remediation approaches may be called for in uranium-contaminated subsurface environments that contain significant concentrations of O 2 and NO 3 Ϫ entering through vertical recharge or lateral transport. One such potential strategy is immobilization of uranium through precipitation of U(VI)-bearing calcium-phosphate (Ca-P) phases (6, 39). Uranium incorporation into Ca-P minerals is a naturally occurring process. For example, U(VI)-phosphate phases at a weathered portion of the Coles Hill, VA, uranium ore deposit maintain groundwater U(VI) concentrations at ca. 0.06 M (11, 12). The shallow portion of this deposit exhibits a sharp Fe redox front with U(IV) assemblages (containing uraninite, UO 2 ) located on the reduced side and U(VI) assemblages [containing autunite, Ca(UO 2 ) 2 (PO 4 ) 3 , and other uranium-bearing Ca-P phases] on the weathered oxidized side. Interestingly, uranium concentrations on both oxidized and reduced sides of the redox front are similar, suggesting no significant uranium loss as a result of oxidation and weathering.A major limitation for engineering uranium immobilization through coprecipitation with Ca-P minerals is the potential decrease in hydraulic conductivity of sediments due to rapid mineral precipitation at or near the point of P i injection. In order to avoid this, P i...