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Dames & Moore, 1999 - USDA Forest Service

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Set 1B: RI stations located in Holden Creek, Big Creek, Copper Creek, Ten Mile Creek<br />

and Stehekin were pooled.<br />

The number of data points for Sets 1A and 1B are shown below. The specific data points used for the<br />

analyses are shown in Tables 5.3-2 through 5.3-14.<br />

Aluminum<br />

Arsenic<br />

Beryllium<br />

Cadmium<br />

Chromium<br />

Copper<br />

Iron<br />

Lead<br />

Magnesium<br />

Manganese<br />

Selenium<br />

Silver<br />

Zinc<br />

Metal<br />

Set lA<br />

Railroad Creek<br />

# Data Points<br />

30<br />

11<br />

21<br />

28<br />

22<br />

2 1<br />

27<br />

22<br />

27<br />

27<br />

10<br />

28<br />

3 1<br />

Set lB<br />

Other Background<br />

# Data Points<br />

13<br />

8<br />

13<br />

13<br />

12<br />

12<br />

13<br />

13<br />

13<br />

9<br />

6<br />

13<br />

13<br />

The Ecology guidance notes that MTCA has no provisions for excluding statistical outliers that have not<br />

resulted from apparent errors. For this reason, all results for the selected sample points that were reported<br />

above the detection limit were included in the statistical calculations. However, due to the wide.range of<br />

detection limits reported historically and during the RI, some data points (reported as not detected) were<br />

omitted if the detection limits reported were due to apparent methodology differences that resulted in high<br />

detection limits that were well above the other reported data. Historically and during the RI, method<br />

changes were made in an effort to reduce detection limits so that the data were more meaningful when<br />

compared to water quality criteria (WQC). Tables 5.3-1 through 5.3-14 show the data points actually<br />

used for each analysis as well as those considered for analysis but omitted.<br />

During RI data collection in 1997, lead results in upstream stations were generally at or just above the<br />

detection limit of the method used for analysis. Due to continuous method blank contamination in the<br />

laboratory, detected surface water sample lead results were artificially influenced. This, in combination<br />

with the need to clearly delineate lead concentrations above chronic water quality criteria, resulted in a<br />

revision to the lead method in 1998 to reduce the detection limit by an order of magnitude. Detection<br />

limits ranged from 0.01 1 to 1 pg/L in sample data collected during the RI. Due to the wide range of<br />

concentrations representing the detection limit, the 90th percentile calculated for lead in all three data sets<br />

did not include detection limits greater than or equal to 1.0 pg/L. Inclusion of these detection limits<br />

skewed the 90th percentile lead concentration. Table 5.3-9 provides a list'of sample data points that were<br />

considered but were omitted from the statistical calculations.<br />

An additional item considered during the. statistical analysis for zinc was the impact of field filtration<br />

during April, May, June, and July 1997. During this timeframe, it was determined that field filtration had<br />

potentially artificially enhanced the zinc results. For statistical purposes, the total results were used where<br />

the data for dissolved zinc clearly indicated artificially introduced zinc. These instances include only the<br />

\UlM-SEA I\VOLI\COMMOMWP\WPDATAU)O5\REPORTSWOLDEN-2UUU doc 5- 1 7 DAMES & MOORE<br />

17693-005-019Uuly 28. <strong>1999</strong>;11:09 AM:DRAFT FINAL RI REPORT

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