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Dames & Moore, 1999 - USDA Forest Service

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The pH to copper relationship (Figure 6.4-12) shows some indication of pH controls. Copper is higher in<br />

concentration in the west area of the site than the east area. The abandoned mill building, portal drainage<br />

and waste rock piles indicate a negative correlation between copper and pH implying a constraint on<br />

copper concentrations for these data. In comparison, much lower copper concentrations are seen in the<br />

tailings pile seeps. The data do not have sufficient pH range to demonstrate a relationship between<br />

copper and pH, though tailings pile 1 has lower copper concentrations at higher pH. The tailings pile data<br />

probably indicate a limit to the availability of copper in the tailings but also possibly indicate the effects<br />

of co-precipitation of ferric hydroxides. In the case of limited copper availability in tailings, the<br />

correlation of pH and copper reflects only the increased leaching of copper by stronger acidic solutions.<br />

Copper concentrations in surface waters of Railroad Creek are very low and do not appear to be<br />

controlled by the solubility of copper secondary minerals. Coprecipitation and adsorption on iron<br />

coatings and other materials on stream sediments is expected to attenuate copper concentrations in stream<br />

waters.<br />

The plot of pH and zinc (Figure 6.4-13) is similar to copper except that the mill building, portal drainage<br />

and waste rock piles appear to have relatively stable zinc concentrations (between 0.1 and 1 m a). This<br />

may imply a mineral solubility constraint, although zinc minerals are far more soluble than indicated by<br />

these data. The tailings pile data appear to indicate a limit to the availability of zinc, as zinc would be<br />

expected to occur at much higher concentrations in low pH water (by extrapolation of the pH to zinc trend<br />

for the mill building, portal drainage, and waste rock piles). The correlation of zinc and pH may, like<br />

copper, be caused by co-precipitation of zinc with ferric hydroxides, with the effect decreasing as pH<br />

decreases. omp par is on of sulfate and aluminum also supports the general conclusion of buffering by<br />

alumino-silicates (Figure 6.4-9) shown by examination of magnesium and potassium concentrations.<br />

sulfate is correlated with aluminum at high aluminum and sulfate concentrations indicating that<br />

generation of acid, represented by sulfate results in attack on alumino-silicates releasing aluminum in<br />

proportion to acidity. However, aluminum concentrations are lowered by aluminum hydroxides<br />

precipitation, hence the relationship is only stable at higher sulfate and lower pH. Aluminum is removed<br />

rather than sulfate as pH increases introducing scatter in the relationship between the parameters in Figure<br />

6.4-9.<br />

The cadmium to pH relationship is similar to Zn-pH indicating that zinc and cadmium show similar<br />

geochemical behavior (Figure 6.4- 14).<br />

Water ch'emistry indicates that pH is controlled by the formation of amorphous hydroxide precipitates of<br />

iron and aluminum. The formation of these precipitates constrains pH, which allows copper to remain in<br />

solution, but precipitation also allows attenuation by co-precipitation and provides a substrate for<br />

adsorption.<br />

6.4.6 Conclusions<br />

Evaluation of water chemistry .indicates that geochemical behavior consistent with the well-known<br />

processes discussed in Section 6.3 is occurring throughout the Holden Mine Site. Conclusions fiom this<br />

section are as follows:<br />

Consistent geochemical processes are occurring throughout the Site, specifically iron<br />

sulfide oxidation, sphalerite and chalcopyrite oxidation, buffering and metal attenuation.<br />

\\DM-SEA I\VOLI\COMMOMWP\~W)~~2\n160.dos 6-23<br />

17693-005-019Vuly 27.<strong>1999</strong>.4:ll PMDRAFf FINAL RI REPORT

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