This study uses fluorescence spectroscopy to better understand the role of environmental metal ions in the interaction of charged herbicides with biochemical degradation product Suwannee River fulvic acid (SRFA). The interactions between the widely-used herbicide dichlorprop (2-(2,4-dichlorophenoxy)propionic acid) (DCPPA) with Al(3+) and the comparative metal Er(3+) were probed at pH 4.0. Fluorescence experiments on binary solutions at pH 4.0 clearly indicated that Al(3+) and Er(3+) strongly interact with both SRFA and DCPPA alone in solution as demonstrated by fluorescence quenching with DCPPA and enhancement with SRFA by Al(3+) and fluorescence quenching of both SRFA and DCPPA fluorescence by Er(3+). Titrating Al(3+) or Er(3+) to SRFA-DCPPA quenched SRFA fluorescence as compared to the SRFA-metal ion binary complexes. Formation constants were determined using the Ryan-Weber model for the titration data. The DCPPA fluorescence results strongly support the formation of DCPPA-Al(3+) and DCPPA-Er(3+) complexes at pH values above the pK(a) (3.0) of DCPPA. Excitation and emission data obtained on ternary solutions of SRFA-Al(3+)-DCPPA and SRFA-Er(3+)-DCPPA complexes at pH 4.0 suggest that at this pH where the predominant DCPPA species is negatively-charged, Al(3+) and Er(3+) metal ions may function to "bridge" negatively-charged fulvic acids to negatively-charged pesticides. Fluorescence data collected on UV-irradiated ternary complexes indicate that both metals can also bridge DCPPA interactions with SRFA under those conditions. The results of our studies suggest that creation of a herbicide-free boundary corridor is recommended near mines and runoff areas with metal ions in surface waters to control possible complexation among fulvic acids, DCPPA and metal ions that maintains these molecules in a bioavailable state to plants and animals.

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http://dx.doi.org/10.1016/j.jinorgbio.2011.08.009DOI Listing

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