The most commonly used tracers to probe the atmospheric and biogeochemical cycles of CO 2 are 16 17 O over δ 18 O alone lies on the sensitivity of the former to the rates of biogeochemical processes involving multiple water reservoirs with spatial and temporal isotopic heterogeneities. To employ all the three oxygen isotopes for estimating fluxes of CO 2 , sources and processes affecting their partitioning have to be identified and quantified. Here, we measured ∆ 17 O values in near surface atmospheric CO 2 from Taiwan in urban and semi-urban areas and over the South China Sea. Strong spatiotemporal variation was seen, with an average ∆ 17 O value of 0.332‰ and a mean variation of 0.043‰ (relative to V-SMOW; 1-σ standard deviation for a total of 140 samples). The large variation reflects combinations of distinct air masses carrying CO 2 from sources having different ∆
17O values: negative from combustion emissions, positive from the stratosphere, and a positive water-CO 2 equilibration value from isotope exchange with leaf/soil/ocean waters. We observed that the variation of the semi-urban ∆ 17 O values is largely affected by local biogeochemistry and stratospheric intrusion with only minor influence from anthropogenic emissions. This is the first oxygen anomaly study for near surface CO 2 covering diverse source characteristics and has enormous potential in air CO 2 source identification and constraining the global carbon budget.