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Dames & Moore, 1999 - USDA Forest Service

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Evidence of significant surface and channel erosion in Site drainages was not observed and therefore,<br />

there does not appear to be a direct water borne pathway for significant quantities of metal-containing<br />

sediments to enter Railroad Creek fiom the Site. Under extreme flow events, bank erosion in Railroad<br />

Creek and channel shifting with subsequent erosion of tailings in Copper Creek can potentially transport<br />

tailings into Railroad Creek. Channel scour and re-suspension of flocculent and fine particulates<br />

originating as iron oxide (and other) metal precipitates, and which settle into the Railroad Creek<br />

streambed, is also a transport mechanism which can carry metals downstream. Although large channel<br />

scour events in Railroad Creek which transport bed material long distances downstream are not common<br />

(due to the size of the dominant bed material and bed armoring), transport of iron-oxides as fine<br />

suspended material was observed several times during high flow events in 1997.<br />

63 GEOCHEMISTRY INTERPRETATION TOOLS<br />

Interaction of minerals with the atmosphere and the formation of new minerals control the chemistry of<br />

waters originating from the Site. A critical component of the geochemical interpretation is therefore the<br />

determination of which minerals in the rocks are controlling the original source of the water, and which<br />

new minerals are forming and removing metals from solution. These two groups of minerals are referred<br />

to as primary, indicating that they are present in the rocks, and secondary, indicating that they are formed<br />

when metals released from the primary minerals react with other dissolved or solid constituents. The first<br />

group does not include all minerals in the rocks because some minerals are inherently unreactive.<br />

The following subsections describe the interpretative tools that were used to evaluate chemical processes<br />

occurring at the Site.<br />

6.2.1 Contribution of Primary Minerals<br />

Subsection 6.1.1 described the types of primary minerals reported to be present in the rocks within the<br />

Holden Mine. The processes that contribute the components of primary minerals to mine water chemistry<br />

are introduced below and described in more detail in'subsection 6.3.<br />

The controlling process on water chemistry at the Site is the oxidation of iron sulfide (pyrite),<br />

summarized as:<br />

The acid (IT) produced by this reaction, can then dissolve other minerals, for example, calcite:<br />

or, other more abundant minerals (for example, potassium feldspar):<br />

It can be seen from reaction (6-1) that each mole of pyrite produces two moles of sulfate ion and four<br />

moles of hydrogen ions (representing acidity). Reactions (6-2) and (6-3) indicate that these four hydrogen<br />

ions then react with calcite and produce two ions of calcium or four ions of potassium. Therefore, if<br />

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