The mineral-water interface exhibits great diversity in surface functional group composition and associated reactivity towards inorganic and organic solutes that occur in natural soil, sediment and water. [1,2] Chemical processes of environmental significance involving oxidation-reduction, adsorption-desorption, and dissolution-nucleation are promoted by these interfaces because of their propensity for acid-base, ion-or ligandexchange, and redox reactions. Mineral surface hydroxyl groups of iron, aluminium and manganese (oxyhydr)oxides and siloxane groups of layered aluminosilicates, for example, are known to exhibit a range in affinities for reaction with protons, hydroxyl ions, metals, oxyanions, and aqueous organic species and their complexes. [3] The environmental implications of mineral surface chemistry are manifold and diverse. They include atmospheric CO 2 drawdown associated with silicate mineral dissolution, [4,5] removal from solution of adsorptive metal and oxyanion contaminants, [6] nutrient retention for plant growth [7] and organic matter stabilisation against microbial biodegradation. [8] Through a combination of macroscopic experiments, molecular spectroscopy studies, and molecular modelling, environmental chemists are developing an improved understanding of the molecular-scale controls over the rates and extents of mineral surface reactions.This Research Front presents six contributions discussing various aspects of mineral surface reactions and their environmental relevance using experimental, spectroscopic and simulation methods. The Research Front begins with a review by Casey [9] on the mechanisms and kinetics of ligand exchange reactions at mineral surfaces. This paper discusses reactivity trends for ligand and oxygen isotope exchanges in nanometresized molecular clusters and larger mineral structures from the perspective of coordination chemistry. It provides examples of how an understanding of exchange reactions in the molecular clusters can shed light on reaction kinetics of broad environmental relevance, such as those for mineral dissolution and metal-ligand complex formation in aqueous solutions.The second paper, a review by Stack and Kent, [10] discusses how computational modelling, specifically molecular dynamics and quantum chemical simulations, can be used to build insightful kinetic models of mineral surface reactions. Illustrative examples are presented for water ligand exchange, adsorption, crystal growth, dissolution and electron transfer. Interfacial reactions are strongly affected by the speciation of aqueous phase reactants as shown in the third paper, authored by Carbonaro and Stone. [11] This study, which evaluates mineralsurface-mediated rates of Cr III oxidation to Cr VI during surface reaction with hydrous Mn IV oxide, shows that Cr III -chelating ligands alter the pH-dependent kinetics of oxidation. This is important, because most soil systems contain natural organic matter (NOM) that can form stable complexes with polyvalent metals.The fourth paper by Pasakarnis et a...