We investigated groundwaters in the vicinity of a coal ash site near an electric generating station in the western U.S.A. The purpose of the study was to ascertain why fine particles or colloids appear in some subsurface water samples there. If such fine particles are merely introduced during bailing or pumping operations which suspend otherwise immobile soil colloids, we should exclude these particulate materials from the water samples before analysis intended to quantify what is moving through the aquifer. However, if the colloids were truly suspended and moving with the groundwater flow in situ, then we should includes their contribution to our assessment of the mobile loads. Application of very careful sampling techniques (slow pumping rates, no atmospheric exposure) did not cause the large quantities of colloids observed previously to disappear from well water in which they occured. Additionally, the same sampling procedures did not cause similar abundances of colloids to appear in waters collected from neighboring wells installed and developed in the same manner and in the same geologic strata. Thus we believe sampling artifacts do not explain the colloids' presence in the groundwater samples. On the other hand, the groundwater chemistry and the nature of the suspended colloids (size, composition) strongly suggest these fine particles were suspended and therefore moving with the groundwater flow. At wells exhibiting large amounts of suspended colloids (≈10–100 mg L −1), the water was enriched in CO 2 and depleted in O 2 relative to nearby locations. The colloids were typically between 0.1 and 2 μm in size and were primarily silicates. These results suggest to us that, where infiltrating water is percolating through a site that has been mixed with coal ash, the secondary carbonate mineral in the soils are being dissolved; removal of this cementing carbonate phase may consequently release soil silicate colloids to be carried in the flowing water. Such processes may enhance contaminant transport in groundwater by augmenting the pollutant load moving in the groundwater, and increasing the permeability of the porous medium to pollutant infiltration with water water and/or rainwater.