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"19, 63, 212, 319". If the values listed on Plate 19 are correct,then the result of the <br /> Acid/Base Accounting Flowsheet on Plate 25 (assuming oxidation of the vadose zone) <br /> would be 88 million tons CaCO3 equivalent exiting the Carlton Tunnel (rather than 30 <br /> million tons). Please correct or explain this discrepancy. <br /> RESPONSE. The set of values cited by DRMS differ because the Plate 19 values refer to <br /> the total rockmass, while the Plate 25 values refer to the unmined vadose zone rockmass. <br /> The difference is the mined vadose zone rockmass, which is accounted for separately in <br /> Plate 25 under the column "Mined Rock Acid Generation (million tons CaCO3)". The <br /> ABA results have been further checked as a result of this question, and are correct. <br /> Additionally, in the Acid Neutralization Computation table, for Cell 2: Vadose Zone Rock, <br /> under the column Vadose Zone Acid Neutralization(million tons CaCO3), the first four <br /> values listed are"7, 15, 56, 181". However, on Plate 20—Acid Neutralizing Potential,the <br /> values associated with these elevations are listed as"9, 21, 61, 191". If the values listed on <br /> Plate 20 are correct(and the values above for Vadose Zone Acid Generation are corrected <br /> to the values listed on Plate 19),then the result of the Acid/Base Accounting Flowsheet on <br /> Plate 25 (assuming oxidation of the vadose zone)would be 64 million tons CaCO3 <br /> equivalent exiting the Carlton Tunnel(rather than 30 million tons). Please correct or <br /> explain this discrepancy. <br /> RESPONSE. The set of values in cited by DRMS differ because the Plate 19 values refer <br /> to the total rockmass, while the cited Plate 25 values refer to the unmined vadose zone <br /> rockmass. The difference is the mined vadose zone rockmass, which is accounted for <br /> separately in Plate 25 under the column "Mined Rock Acid Neutralization (million tons <br /> CaCO3)". The ABA results have been further checked as a result of this question, and are <br /> correct. <br /> 4.2.3 Static Evaluation of Performance of the Groundwater Neutralizing System <br /> • Page 24: The text summarizes that"the acid generated by the mined material to the <br /> completion of AM-I I will be readily neutralized by the in-situ inventory of calcium <br /> carbonate." And that the "very slow—natural weathering rate—oxidation of the material <br /> in the vadose zone can also be accommodated by the system neutralization, providing <br /> permanent protection against the flow from the Carlton Tunnel turning acidic."The rocks <br /> of the mining district are, in general,net acid producing with twice as much acid <br /> generating potential than acid neutralizing potential,and the system neutralization is based <br /> solely on the currently saturated bedrock remaining saturated. Therefore, as mentioned <br /> above, if the diatreme water table were to drop,there may be a significant loss in the <br /> system's neutralization potential, potentially creating acid rock drainage at the Carlton <br /> Tunnel portal. In this case,there would be no "permanent protection from the flow from <br /> the Carlton Tunnel turning acidic". Have you developed a plan to mitigate impact to <br /> Fourmile Creek if this situation were to occur during the operation,or post-mining? <br /> RESPONSE.DRMS is not entirely correct in stating that "the system neutralization is <br /> based solely on the currently saturated bedrock remaining saturated. " The system <br /> neutralization in the long-term case is based on all the material in the system yielding its <br /> entire neutralizing capacity, which is considered to be reasonable in the long term. It is <br /> the system acidification that is dependent on the location of the water table: if the water <br /> table were to drop below the current average elevation (which is estimated to be 7,500 ft <br /> amsl in these computations and is likely higher, but can never be lower than 6,985 ft amsl, <br /> the elevation of the Carlton Tunnel), then more sulfide would be exposed to potential <br /> oxidation—at natural geological rates—and there would be a somewhat larger shortfall <br /> Page 12 of 28 <br />