Laserfiche WebLink
Cleanup in Vulnerable Communities'Initiative Final Project Reference:Bobson Cleaners <br /> Discovery and Enforcement Discovery Project Number:60688620-5.1 <br /> Investigation Work Plan <br /> Accuracy of laboratory analyses will be assessed by laboratory control samples, surrogate standards, matrix spikes, <br /> and initial and continuing calibrations of instruments. Laboratory accuracy is expressed as the percent recovery(%R). <br /> Accuracy limits are statistically generated by the laboratory, required by specified USEPA methods. If the percent <br /> recovery%R is determined to be outside of acceptance criteria, associated data will be qualified. The calculation of <br /> percent recovery%R is provided below: <br /> % R= 100 (Xs—X)/T, <br /> where Xs is the measured value of the spiked sample,X is the measured value of the unspiked sample, and <br /> T is the true value of the spike solution added. <br /> Field accuracy will be assessed through the analysis of field equipment blanks,where appropriate.Analysis of blanks <br /> will monitor errors associated with the sampling process including equipment decontamination procedures,field <br /> contamination,sample preservation, and sample handling. The DQO for field equipment blanks is that all values are <br /> less than the reporting limit for each target constituent. If contamination is reported in the field equipment blanks, data <br /> will be qualified. <br /> 4.2.3 Representativeness <br /> Representativeness is the degree to which data accurately and precisely represent a characteristic, an environmental <br /> condition, or a population. It relates both to the area of interest and to the method of taking the individual sample. <br /> Representativeness of data collection is addressed by careful preparation of sampling and analysis programs, <br /> including use of procedures to avoid false negatives and false positives (USEPA 2004).This Work Plan addresses <br /> representativeness by specifying sufficient and proper numbers and locations of samples; incorporating appropriate <br /> sampling methodologies; specifying and performing proper sample collection and preservation techniques; <br /> performing required decontamination procedures; selecting appropriate laboratory methods to prepare and analyze <br /> soil, soil gas, and groundwater samples; and establishing proper field and laboratory QA/QC procedures for the <br /> parameters of interest. <br /> 4.2.4 Completeness <br /> Completeness is the amount of valid data obtained compared to the amount expected under ideal conditions. The <br /> number of valid results divided by the number of possible results,expressed as a percentage, determines the <br /> completeness of the data set.The DQO for completeness is to obtain valid results for at least 90 percent of the <br /> planned analytical results.The formula for calculation of percent completeness is presented below: <br /> % Completeness= 100 x(number of valid results)/(number of expected results) <br /> 4.2.5 Comparability <br /> Comparability is an expression of confidence with one data set compared to another. This QA/QC plan addresses <br /> comparability by specifying laboratory methods that are consistent with the current standards of practice as approved <br /> by the USEPA and the DTSC,which will allow the data to be evaluated for trends or changes(in space or time)at the <br /> Site(USEPA 2004). In addition, comparability is also addressed by specifying that associated standard units of <br /> measurement will be used for data reports. <br /> 4.2.6 Method Detection Limits <br /> Method detection limits(MDLs)should be below the screening levels, or else there is no way to know whether non- <br /> detect results are above or below the action level. For this DI,the ultimate action levels will be health-based criteria <br /> calculated in accordance with the methodology set forth in Programmatic QAPP using available cancer potency slope <br /> factors and non-cancer reference doses established by the California Office of Environmental Health Hazard <br /> Assessment(OEHHA), USEPA, or other organizations. However, it is impracticable to calculate all of these action <br /> levels in advance for all of the analytes.Therefore,for the purposes of this QAPP plan,the planned MDLs for <br /> groundwater samples have been compared with the Preliminary Remediation Goals (PRGs)published by USEPA <br /> Region IX(including the Cal/EPA-modified PRGs)to verify that all MDLs are below their respective PRGs, with the <br /> exception of arsenic(typical background concentrations of arsenic in California soil are above the MDL,so the <br /> arsenic MDL is considered acceptable).The planned MDLs for soil gas samples comply with the Programmatic <br /> QAPP. <br /> Prepared for: Department of Toxic Substances Control AECOM <br /> 25 <br />