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• <br /> Dry Wells Remedial Investigation <br /> Lawrence Livermore National <br /> Laboratory Site 300 <br /> San Joaquin County -2- 21 September 1990 <br /> Please note that the State Action Levels listed in RI Table 4 and Addendum Table 2 for <br /> the halogenated volatile organic compounds should be in ug/l , not in mg/l . <br /> Cleanup Levels <br /> LLNL inappropriately persists in using the Title 22 Soluble Threshold Limit <br /> Concentrations (STLC) as pollutant cleanup levels in soils. On the contrary, the STLC <br /> and the Total Threshold Limit Concentrations (TTLC) establish the line between <br /> nonhazardous and hazardous wastes for disposal purposes; for example, hazardous wastes <br /> require disposal in a Class I landfill , while nonhazardous waste may be disposed of <br /> less restrictively. Cleanup levels should be established via site-specific <br /> environmental fate analyses and risk assessments outlined in the Department of Health <br /> Services' Decision Tree Manual , Marshack 's staff report, and other sources. <br /> Additionally, the STLC should not be used as a cleanup criterion because it provides <br /> insufficient information on constituent distribution between the adsorbed, dissolved, <br /> and fixed phases in the polluted soils. The leachable constituent concentrations are <br /> measured, via the Waste Extraction Test (WET) specified in §66700, for comparison to <br /> the STLC criteria listed in Title 22 §66699. The constituent fraction leached into the <br /> test extract provides no information regarding the phase distribution mentioned above. <br /> An adequate environmental fate analysis should be able to consider this distribution <br /> to estimate the extent a constituent may migrate or react in the soil . <br /> Finally, the WET extractant (citric acid - citrate buffer solution) can cause major <br /> changes in the soil environment of the sample, rendering the results of the test <br /> unrepresentative. For metals, in particular, <br /> "These gross alterations result from the fact that the extractants can (a) <br /> selectively dissolve soil minerals, (b) impede crystallization and formation of <br /> aluminum hydroxides and other soil minerals while causing structural distortions <br /> in newly formed minerals , (c) perturb hydrolytic reactions of aluminum, and (d) <br /> desorb, via mass action, elements and organics from soil adsorption sites which may <br /> not normally be desorbed. Because the extractants cause gross alterations in the <br /> chemical properties of soil systems, the data derived from these test methods, when <br /> the soil is utilized as the solid phase, cannot be extrapolated to actual field <br /> conditions. Therefore, they should not be used as soil cleanup criteria [for] <br /> spills of hazardous materials. " [James Dragun, The Soil Chemistry of Hazardous <br /> Materials, Hazardous Materials Control Research Institute, 1988] <br /> Altering the soil chemistry with the extractant may also affect the phase distribution <br /> in the soil of the halogenated volatile and other organic compounds further <br /> invalidating use of the STLC as cleanup levels for these compounds. <br /> Sources of Drinking Water <br /> In both the reports reviewed, LLNL states "the nearest water body to be protected is <br /> the regional water-bearing zone, which lies at least 100 feet beneath the dry wells". <br /> In 1988, the State Water Resources Control Board adopted Resolution No. 88-63 <br />