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Dames & Moore, 1999 - USDA Forest Service

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December 1 1, 1998<br />

Sediment Data, Fall 1998, Holden Minc<br />

Page 4<br />

2. Initial Calibration - Acceptable<br />

3.<br />

Applicable to AVS and TOC analyses only.<br />

' Continuing Calibration - Acceptable<br />

Applicable to AVS and TOC analyses only.<br />

4. Blanks - Acceptable<br />

5. Laboratory Control Sample (LCS) - Acceptable<br />

Applicable to pH, AVS, and TOC analyses only.<br />

6. Laboratory Sample Duplicate - Acceptable . .<br />

Per PSEP guidelines for grain size analysis, one sample was analyzed in triplicate.<br />

7. Field Duplicate - Acceptable<br />

Field replicates were collected and labeled LUC-SED-101598-1A; -1 B, and -1 C. Results<br />

indicate that total solids are similar. TOC, N S, AVS, and pH results indicate variability. The results did<br />

not indicate variability related specifically to a sample but variability by analytical method from sample to<br />

sample. It appears that the variability is not due to sampling technique but specifically to individual<br />

sample content. Data were not qualified based on field replicate results.<br />

8. Matrix Spike (MS) -Acceptable<br />

Applicable to AVS and TOC analyses only.<br />

9. Detection Limits - Acceptable<br />

10. Type of Review - Summary<br />

1 1. Overall Assessment of Data<br />

The u.sefulness of the data is based on EPA guidance documents listed above. Upon<br />

consideration of the information presented above, the data are acceptable except where flagged with<br />

data qualifiers that modify the usefulness of the individual values.<br />

Data Qualifiers<br />

U The analyte was analyzed for, but was not detected above the reported sample quantitation limit.<br />

J The analyte was positively identified; 'the associated numerical value is the approximate<br />

concentration of the analyte in the sample.<br />

UJ The analyte was not detected above the reported sample quantitation limit. However, the<br />

'<br />

reported quantitation limit is approximate and may or may not represent the actual limit of<br />

quantitation necessary to accurately and precisely measure the analyte in the sample..<br />

DAMES & MOORE

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