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Red Creek Quarry Baseline Water Investigation Section 4 <br /> <br /> <br />4-7 <br />DRAFT for review purposes only. Use of contents on this sheet is subject to the limitations specified at the end of this document. <br />Laboratory deionized water, devoid of all dissolved ions, was generated by SGS Laboratories. <br />Commercially available distilled water is produced through boiling then condensing water to remove <br />ions and impurities. A sample of the commercially available distilled water used to generate the <br />equipment blank was collected during the May 2023 sampling event to evaluate the level of <br />constituents in the commercially available distilled water for comparison with the equipment blank <br />results. The distilled water blank was field filtered, preserved, analyzed for the same suite of <br />constituents as the equipment blank sample. <br />Results from the equipment blank and distilled water analysis indicate the commercially available <br />distilled water contains low concentrations of ammonia, boron, magnesium, sodium, and manganese <br />(Appendix E). The concentrations of these metals/metalloids in the distilled water are either orders <br />of magnitude below water quality standards or no standard exists for the analyte. Results from the <br />field blanks indicate low concentrations of ammonia, barium, boron, iron, fluoride, sodium, <br />manganese, zinc and total dissolved solids (TDS). Analytes detected in the equipment blanks are <br />flagged as estimated due to the very low concentrations detected between the method detection and <br />reporting limit. Low concentrations of constituents in the equipment blanks may be due to residual <br />groundwater on the water level meter after decontamination or the water used to clean the <br />equipment. The low concentrations in the equipment blank samples compared to the groundwater <br />well samples indicate the decontamination processes used were affective at preventing cross <br />contamination between groundwater wells. <br />4.5.3 Data Validation and Data Review Procedures <br />Laboratory analytical data were reviewed for completeness and validated as described in the QAPP. <br />Data were validated according to the protocols and QC requirements of the specific analytical <br />methods, including a review of the following criteria: <br />• Data completeness <br />• Holding times and sample preservation <br />• Field duplicate accuracy <br />• Surrogate recoveries <br />• Laboratory control sample recoveries <br />• MS and MSDs <br />• Method and field blank contamination <br />• Initial and continuing calibration summaries <br />• Compound quantitation <br />• Reporting limits <br />• Sample comments and laboratory quality control summaries <br />Results qualified as estimated (J flagged) or rejected as unusable (R flagged) were assigned reason <br />codes to indicate any QC parameter that did not meet the data objectives. Data qualified as <br />estimated are considered usable for the intended purpose; however, the reported result may not be <br />accurate or precise. <br />Sampling results, including data qualifiers, are discussed further in the data validation reports <br />(Appendix E). <br />