From a simple conceptual model, the behaviour and source of trace elements in a sandy aquifer in the Netherlands is explained. Groundwater from multilevel well screens in a sandy fresh water aquifer was analyzed by ICP-MS, resulting in a comprehensive set of trace elements analyses that could be interpreted in terms of saturation, co-dissolution/ precipitation, and input and cation exchange. Pure phase equilibrium modelling explained few major and trace elements (Al, P, Ca, Mn, Fe, Ba, and U). Arsenic is explained by codissolution from Fe hydroxides, and Ba and Sr by dissolution of calcite. For Mn coprecipitation with Fe controls concentrations in reduced siderite saturated water. Molybdenum, U, Mn, and possibly Sb are separately controlled by redox conditions. In shallow parts of infiltration areas, weathering of Al-silicates caused by acidification results in anomalous concentrations of Ni, Co, Zn, Be, Cd, Tl, Ga, and REY. Many elements were found to be best explained by source-term limitation from surfacial input, where the sorption complex starts acting as the control upon a disturbance. This enabled identification of anomalies related to specific environments or processes: enhanced Co, Ni, and Zn in acid, reduced waters; mobilization of Ni and Co at reduction and buffering boundaries; slow incongruent release of Li, Rb, and Cs; and pollution (e.g. B, Ti, Cu, Rb, Sb, Tl, Pb).