Dissolved inorganic carbon (DIC) is an important parameter to characterize the biogeochemical processes in sea ice and across the ocean-sea ice-atmosphere interface. The main challenge in bulk sea ice processing for DIC analysis is to melt the ice core without exposure to the air, which otherwise might contaminate the sample. A common practice is to seal the ice core in a gas-tight plastic bag and remove the air gently using a syringe or a hand pump. However, this procedure is time-consuming and the uncertainty in DIC concentration processed in this way has not been fully accessed. In this study, we modified the method by using a vacuum sealer and evaluated this procedure by examining the impact of ice sample processing, biological activity, gaseous CO 2 initially present in sea ice, and the presence of ikaite (CaCO 3 Á6H 2 O) crystals. The results show that no loss or gain in DIC occurs during the evacuation and ice melting process and that it might not be necessary to pre-poison the ice samples during the ice melting process. In addition, gaseous CO 2 initially present in sea ice has a negligible impact on DIC analysis. If detectable ikaite crystals are present in sea ice, the measurement results should be referred to total inorganic carbon instead of DIC. The field test at Station Nord in Greenland demonstrates that the modified method is simple and quick to use even under the most remote and extreme environments.When sea ice grows, most of the brine is expelled to the under-ice seawater due to gravity drainage, while a small portion stays trapped in the ice matrix (Niedrauer and Martin 1979). The chemical composition of brine is primarily a function of salinity and temperature, but can be modified by biological activity and abiotic processes such as gas exchange and mineral formation (Papadimitriou et al. 2007).Dissolved inorganic carbon (DIC) in sea ice, the measurement of which could include gaseous CO 2 in the bubbles of the ice, is an important parameter to describe the ocean-sea ice-atmosphere CO 2 flux. As described in Tison et al. (2002), sea ice was for many years considered as a lid over seawater preventing CO 2 exchange between the atmosphere and ocean. Some observations suggest that sea ice can be an active source or sink for CO 2 (e.g., Nomura et al. 2010;Miller et al. 2011). A more recent study shows that the effective gas velocity decreases in proportion to sea ice cover, suggesting that CO 2 flux through sea ice could be minor (Butterworth and Miller 2016). However, direct measurements of the CO 2 flux on sea ice based on the chamber method and eddy covariance tend to largely disagree as pointed out in Geilfus et al. (2013). Since the ice-atmosphere CO 2 flux is limited by the DIC stocks in sea ice (Moreau et al. 2015), improved measurements of DIC in sea ice are needed to better understand the air-ice CO 2 flux. Rysgaard et al. (2011) proposed a conceptual model describing the role of sea ice in controlling air-sea CO 2 exchange (i.e., sea ice carbon pump), and noted that a large data...