The dissolution rates of olivine have been considered by a plethora of studies in part due to its potential to aid in carbon storage and its ease in obtaining pure samples for laboratory experiments. Due to the relative simplicity of its dissolution mechanism, most of these studies provide mutually consistent results such that a comparison of their rates can provide insight into the reactivity of silicate minerals as a whole. Olivine dissolution is controlled by the breaking of octahedral M 2+-oxygen bonds at or near the surface, liberating adjoining SiO4 4tetrahedra to the aqueous fluid. Aqueous species that adsorb to these bonds apparently accelerate their destruction. For example, the absorption of H + , H2O and, at some conditions, selected aqueous organic species will increase olivine dissolution rates. Nevertheless, other factors can slow olivine dissolution rates. Notably, olivine dissolution rates are slowed by lowering the surface area exposed to the reactive aqueous fluid, by for example the presence and/or growth on these surfaces of either microbes or secondary phases. The degree to which secondary phases decelerate rates