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Site Investigation Work Plan Data Acquisition <br /> Carousel Cleaners, Sacramento, California and QA/QC <br /> 5.3.2 Accuracy <br /> Accuracy is a measure of bias in a measurement system. The closer that the value of the measurement <br /> agrees with the true value,the more accurate the measurement. This value will be expressed as the <br /> percent recovery for any spikes (LCSs and surrogates)as well as calibration recoveries. <br /> 5.3.3 Representativeness for Standard Reference Material <br /> Representativeness is a qualitative parameter that expresses the degree to which sample data accurately <br /> and precisely represent a characteristic of a population,variations at a sampling point, or an <br /> environmental condition. The purpose for sampling, selection of the sampling locations,number of <br /> samples to be collected, ambient conditions, frequencies and times for sample collection, and sampling <br /> techniques have been designed to ensure that the environmental conditions will be sufficiently <br /> represented. <br /> 5.3.4 Comparability <br /> Comparability is a qualitative parameter expressing the confidence with which one data set can be <br /> compared to another. Sample data will be collected and reported consistently,to be comparable with other <br /> measurement data for similar site samples and sample conditions. This goal will be achieved by using <br /> standard operating procedures to collect and analyze representative samples,reporting analytical results in <br /> appropriate and consistent units, and meeting similar accuracy and precision acceptance criteria. <br /> 5.3.5 Completeness <br /> Completeness is defined as the percentage of valid measurements to planned measurements.Valid data <br /> are values that are not rejected for any reason, including deviations from QC requirements. An objective <br /> of the sampling program is to establish the quantity of data needed to support the investigation. This <br /> objective will be achieved by obtaining samples for all types of analyses required at each individual <br /> location; a sufficient volume of sample material to complete the analyses; samples that represent all <br /> possible contaminant situations under investigation; and samples at critical data locations, such as <br /> background and control samples. Completeness will take into consideration adverse environmental <br /> conditions and the potential for justifiable change with respect to schedule and sample locations. The <br /> completeness goal for this project is 90 percent. <br /> 5.4 Quality Control Samples and Procedures <br /> 5.4.1 QC Checks <br /> The QC checks of both field and laboratory sample analysis will be used to assess and document data <br /> quality, and to identify discrepancies in the measurement process that need correction. Field QC samples <br /> may consist of field replicates(duplicates),trip blanks, and temperature blank samples. Laboratory QC <br /> may consist of method calibration,LCS,method blanks, surrogate spikes, and matrix spike/matrix spike <br /> duplicate samples. The analytical laboratory also will report any QC failures, such as calibration check <br /> samples that exceed control limits. <br /> 5-2 <br />