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<br />r,~11?7 <br />t..;J.x.. ~.... <br /> <br />Table 8. Bulk atmospheric-deposition sampling sites <br /> <br />[Identification number is latitude and longitude of the site with a two-digit sequence number at the end; see figure 8 for site location] <br /> <br />Site <br />code <br />PAY <br />GRAV <br />A <br />B <br />C <br />D <br />E <br />F <br />G <br />H <br />J <br />K <br /> <br />u.s. Geological Survey <br />Identlflcallon number <br />394044105420200 <br />393609105423400 <br />392813105403200 <br />392822105410600 <br />393152105434701 <br />393300105431100 <br />393413105432700 <br />393506105430601 <br />393516105430701 <br />393612105423801 <br />394113105420000 <br />394116105414900 <br /> <br />QUALITY ASSURANCE <br /> <br />USGS quality-assurance procedures are standard- <br />ized. Equipment and water-quality meters are regularly <br />checked and calibrated in the field. Deionized water <br />used in cleaning and processing is monitored for purity <br />(Horowitz and others, 1994). <br />Cleaning procedures are rigorous and are designed <br />to prevent contamination of samples. Prior to sample <br />collection. all sampling equipment and materials were <br />cleaned according to standard procedures described in <br />Horowitz and others (1994). The procedures involve a <br />soak and wash in non-phosphorus detergent, soak and <br />rinse in tapwater, followed by a soak and rinse in a <br />5-percent hydrochloric acid solution, and a final soak and <br />rinse in deionized water. The procedure was perfonned <br />for all sampler parts that contact the samples, chum <br />splitter, and the pump tubing for sample filtration. Other <br />procedures for ensuring against sample contamination <br />included clean sample-processing areas, two-person <br />sampling crews, disposable capsule filters, and ultrapure <br />concentrated nitric acid stored in teflon containers for use <br />in sample preservation. <br />Two field blanks were collected during the year, <br />although the results for only one field blank were <br />available. A field blank is produced from water that does <br />not contain the substances in the analysis. Specific types <br />of blank water are used for inorganic and organic blank <br />samples. The field blank showed all analytes to be within <br />the precision of the method, except the dissolved organic <br />carbon sample. Methanol was being used in the field <br />cleaning process for the fIlter apparatus and could not be <br /> <br />Site <br />name <br />Green Lake paved site near Georgetown. Colorado <br />South Clear Creek gravel site near Georgetown, Colorado <br />Grant road site near Grant, Colorado <br />Grant reference site near Grant, Colorado <br />Road site below Mill Gulch near Grant, Colorado <br />Road site above Mill Gulch near Grant, Colorado <br />Geneva Basin Ski Area road site near Grant, Colorado <br />Road site above Duck Lake near Grant. Colorado <br />Road site near Duck Lake near Grant. Colorado <br />Road site below Guanella Pass near Georgetown. Colorado <br />Road site above Georgetown Reservoir near Georgetown. Colorado <br />Clear Creek reference site near Georgetown, Colorado <br /> <br />adequately rinsed from the filter cylinder when consecu- <br />tive samples were being processed. Samples contami- <br />nated by methanol showed up in the analytical data as <br />dissolved organic carbon with a higher value than total <br />organic carbon. The erroneous results were not used, and <br />methanol was eliminated from the cleaning process. <br />A field spike sample was prepared, in addition to a <br />field blank, for each of the trace organic water samples <br />collected. A field spike is prepared by adding a precise <br />amount of a prepared solution containing several of the <br />analytes of interest to organic blank water and analyzing <br />the sample for the percentage recovered. The lab analysis <br />recovered an acceptable amount of the spiked substances <br />in all samples. The results of the field-trace organic <br />blanks indicated that all analytes were less than the <br />reporting limit. <br />When questionable results for a particular analyte <br />were received from the lab. a repeat analysis of the same <br />sample was requested. If the second analysis was more <br />consistent with known characteristics of the site or the <br />particular sample, the new result was used instead of the <br />previous result. There are several samples in which the <br />dissolved concentration of a trace element was reported <br />to be higher than the total recoverable concentration. <br />These inconsistencies are within the precision of the <br />methods used and are due, in part, to the differences in <br />the analytical technique used for dissolved (ICP-MS) <br />and total recoverable trace elements (GF AA or AA), and <br />the differences between particular aliquots of sample. <br />The analytical quality-assurance practices and procedures <br />of the National Water Quality Laboratory are described <br />in Friedman and Erdmann (1982). <br /> <br />QUALITY ASSURANCE 19 <br />