Abstract. The complexity of dissolved gas cycling in the ocean presents a challenge for mechanistic understanding and can hinder model intercomparison. One helpful approach is the conceptualization of dissolved gases as the sum of multiple, strictly defined components. Here we decompose dissolved inorganic carbon (DIC) into four components: saturation (DIC sat ), disequilibrium (DIC dis ), carbonate (DIC carb ), and soft tissue (DIC soft ). The cycling of dissolved oxygen is simpler, but can still be aided by considering O 2 , O 2 sat , and O 2 dis . We explore changes in these components within a large suite of simulations with a complex coupled climatebiogeochemical model, driven by changes in astronomical parameters, ice sheets, and radiative forcing, in order to explore the potential importance of the different components to ocean carbon storage on long timescales. We find that both DIC soft and DIC dis vary over a range of 40 µmol kg −1 in response to the climate forcing, equivalent to changes in atmospheric pCO 2 on the order of 50 ppm for each. The most extreme values occur at the coldest and intermediate climate states. We also find significant changes in O 2 disequilibrium, with large increases under cold climate states. We find that, despite the broad range of climate states represented, changes in global DIC soft can be quantitatively approximated by the product of deep ocean ideal age and the global export production flux. In contrast, global DIC dis is dominantly controlled by the fraction of the ocean filled by Antarctic Bottom Water (AABW). Because the AABW fraction and ideal age are inversely correlated among the simulations, DIC dis and DIC soft are also inversely correlated, dampening the overall changes in DIC. This inverse correlation could be decoupled if changes in deep ocean mixing were to alter ideal age independently of AABW fraction, or if independent ecosystem changes were to alter export and remineralization, thereby modifying DIC soft . As an example of the latter, we show that iron fertilization causes both DIC soft and DIC dis to increase and that the relationship between these two components depends on the climate state. We propose a simple framework to consider the global contribution of DIC soft + DIC dis to ocean carbon storage as a function of the surface preformed nitrate and DIC dis of dense water formation regions, the global volume fractions ventilated by these regions, and the global nitrate inventory.