We recently reported the first multiple oxygen isotope composition of nitrate (NO3-) in ice cores (Alexander et al., 2004). Postdepositional photolysis and volatilization may alter the isotopic signatures of snowpack nitrate. Therefore the precise assessment of the geochemical/atmospheric significance of O-isotopic signatures requires information on the relative rates of photolysis (λ > 300 nm) of N16O3-, N16O217O-, and N16O218O- in ice. Here we report on 17O- and 18O-fractionation in the 313-nm photolysis of 10-mM aqueous solutions of normal Fisher KNO3 (i.e., Δ17O = -0.2 ¿ 0.2?) and 17O-enriched USGS-35 NaNO3 (Δ17O = 21.0 ¿ 0.4?) between -30¿ and 25¿C. We found that Fisher KNO3 undergoes mass-dependent O-fractionation, i.e., a process that preserves Δ17O = 0. In contrast, Δ17O in USGS-35 NaNO3 decreased by 1.6 ¿ 0.4? and 2.0 ¿ 0.4? at 25¿C, 1.2 ¿ 0.4? and 1.3 ¿ 0.4? at -5¿C, and 0.2 ¿ 0.4? and 1.1 ¿ 0.4? at -30¿C, after 12 and 24 hours, respectively. Since the small quantum yield (~0.2%) of NO3- photodecomposition into (NO2 + OH) is due to extensive cage recombination of the primary photofragments rather than to intramolecular processes, the observed Δ17O decreases likely reflect competitive O-isotope exchange of geminate OH-radicals with H2O (Δ17O = 0) and escape from the solvent cage, in addition to residual O-isotope mixing of the final photoproducts NO, NO2, NO2-, with H2O. At the prevailing low temperatures, photochemical processing will not impair the diagnostic value of O-isotopic signatures in tracing the chemical ancestry of nitrate in polar ice.