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Monitoring changes in stable oxygen isotope ratios in molecular oxygen allows for studying many fundamental processes in bio(geo)chemistry and environmental sciences. While the measurement of 18O/16O ratios of O2 in gaseous samples can be carried out conveniently and from extracting moderately small aqueous samples for analyses by continuous-flow isotope ratio mass spectrometry (CF-IRMS), oxygen isotope signatures, δ18O, could be overestimated by more than 6‱ because of interferences from argon in air. Here, we systematically evaluated the extent of such Ar interferences on 18O/16O ratios of O2 for measurements by gas chromatography/IRMS and GasBench/IRMS and propose simple instrumental modifications for improved Ar and O2 separation as well as post-measurement correction procedures for obtaining accurate δ18O. We subsequently evaluated the consequences of Ar interferences for the quantification of O isotope fractionation in terms of isotope enrichment factors by continuous-flow isotope ratio mass spectrometry.