Abstract
Leachate from the North Bay municipal landfill has contaminated an unconfined, sandy aquifer throughout the 700 m flow system from the site to a discharge zone at a creek. The major organic contaminants identified are aromatic hydrocarbons, especially substituted benzenes. The high groundwater velocity of about 75 m yr −1 and the low organic sorption properties of the sand have permitted non-transformed contaminants to spread throughout the total flow system. There is considerable temporal and spatial variability in groundwater chemistry. Most of the aqueous organic carbon has a nominal molecular weight of <2000 and the general decrease in the mass of this fraction relative to Cl indicates it is being mineralized significantly during transport. IR spectra indicate a general trend of increased aromaticity and decreased OH content of organic matter along the flow system. The aqueous organic matter has a significant apparent complexing capacity and so it is somewhat surprising that toxic metal concentrations in leachate-impacted groundwaters are low. In the leachate plume, this complexing capacity is taken up by major cations and H + and to a far lesser extent by toxic metals such as Pb, Cd or Zn. Dispersion is clearly responsible for considerable decrease in contaminant concentration along the flow system. Biotransformation under strictly anaerobic conditions has probably caused 1,1,1-trichloroethane and trichloroethylene to be restricted to the immediate vicinity of the landfill. A simple method of comparing the concentrations of pairs of organics at points along the flow system provides relative transformation rates for pairs of organics even with variable inputs from the landfill and dispersive dilution. Relative to ethylbenzene, o-xylene is rapidly lost from this system. O-xylene may be less persistent than m- or p-xylene; a result unexpected from previous studies of these dimethylbenzenes. In the initial, strictly anarobic segment of the flow system 1,2,4-trimethylbenzene and 1,4-dichlorobenzene are equally persistent, but in the final, less anaerobic segment, the former appears to be degraded more rapidly than the latter. Contaminant distributions in aquifers reflect the results of a number of processes integrated in a complex manner and so are difficult to interpret in terms of specific processes. However, they do provide evidence for what processes are most significant in real groundwater systems and they will also provide critical tests of how well laboratory-derived information relates to real groundwater contamination situations.
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