“…Water extracts are too complex to carry out successful qualitative analyses of mutagens, and some form of separation/fractionation is required. In studies where mutagens in neutral drinking water extracts have been fractionated, the original activity has been distributed among several subfractions, and further fractionation has suffered from difficulties in detecting the diluted activity (21)(22)(23). However, Meier et al (24) found that when the muta-genicity of the extract of strong acids, obtained from an aqueous solution of chlorinated humic acids was fractionated by C18 column HPLC, the activity was concentrated in two distinct subfractions: the fraction collected in the middle of the chromatographic run being twice as active as the fraction which eluted later.…”