[1] High-resolution in situ CO 2 measurements were conducted aboard the NASA DC-8 aircraft during the ARCTAS/POLARCAT field campaign, a component of the wider [2007][2008] International Polar Year activities. Data were recorded during large-scale surveys spanning the North American sub-Arctic to the North Pole from 0.04 to 12 km altitude in spring and summer of 2008. Influences on the observed CO 2 concentrations were investigated using coincident CO, black carbon, CH 3 CN, HCN, O 3 , C 2 Cl 4 , and D 14 CO 2 data, and the FLEXPART model. In spring, the CO 2 spatial distribution from 55°N to 90°N was largely determined by the long-range transport of air masses laden with Asian anthropogenic pollution intermingled with Eurasian fire emissions evidenced by the greater variability in the mid-to-upper troposphere. At the receptor site, the enhancement ratios of CO 2 to CO in pollution plumes ranged from 27 to 80 ppmv ppmv −1 with the highest anthropogenic content registered in plumes sampled poleward of 80°N. In summer, the CO 2 signal largely reflected emissions from lightning-ignited wildfires within the boreal forests of northern Saskatchewan juxtaposed with uptake by the terrestrial biosphere. Measurements within fresh fire plumes yielded CO 2 to CO emission ratios of 4 to 16 ppmv ppmv −1 and a mean CO 2 emission factor of 1698 ± 280 g kg