Speciation controls on Ni adsorption to birnessite and organo-birnessite

Nickel (Ni) is an essential micronutrient for phytoplankton. Its importance to both the modern and ancient Earth system has encouraged development of Ni and its isotopes as biogeochemical tracers. To interpret these signatures however, understanding of how Ni and its isotopes are recorded in marine archives is required. Here we simulate different inorganic and organic Ni species in seawater and investigate their adsorption behaviours to variably crystalline phyllomanganates and organo-mineral phyllomanganate. We conduct pH adsorption edge experiments to determine the binding affinity of the different Ni species to the minerals and then perform desorption experiments to operationally define Ni bonding strength. We also use thermodynamic surface complexation modelling to constrain Ni adsorption mechanisms. From the adsorption edges and stability constants generated from our modelling, the binding affinity increases in the order of Ni-formate+ (aq) < NiCl+ (aq) < Ni2+ (aq). From the desorption experiments, desorption at pH 8 is non quantitative and increases in the opposite order of Ni-formate+ (aq) > NiCl+ (aq) ∼ Ni2+ (aq). For the organo-mineral however, Ni desorption at pH 8 is non quantitative and similar for all three experiments, and is significantly higher compared to the variably crystalline phyllomanganates. Although both our adsorption and desorption experiments were performed over 48 h, it is possible that desorption is somewhat slower than adsorption such that a longer desorption period may result in further Ni loss to solution and thus greater adsorption reversibility. Taken together however, the Ni-formate+ (aq) and Ni organo-birnessite desorption experiments suggest that Ni bonding strength is decreased by the presence of organic carbon, compared to NiCl+ (aq) and Ni2+ (aq). Because bonding strength governs equilibrium stable isotope fractionation, we use our experimental findings to suggest how Ni speciation in seawater might influence Ni isotope behaviour during adsorption to phyllomanganate. We find that our suggestions are consistent with isotopic measurements from natural sediments. Although the balance of Ni adsorption versus incorporation during uptake to phyllomanganates may play a greater part in explaining the variation in the Ni isotope composition in Mn-rich sediments, Ni speciation and the presence of organics might increase the range of δ60Ni values measured in natural settings.