USGS
 Environmental Geochemistry and Sediment Quality in Lake Pontchartrain

Continuous Sediment Sampling and Analysis System

Appendix A.  Quality Assurance and Control

Several steps were taken to ensure that the systems used to perform the survey were operating properly at all times. The methods for the quality assurance and control were documented in the QAPP (CAIS, 1997) for this project. The topics addressed during the quality control measures are addressed in the following text.

    • Precision and accuracy
    • Total sample concentrations
    • Interlab sample comparison

A.1  Precision and Accuracy

A replicate sample analysis was performed for the NIST 2704 wafer. Table A-1 shows the results of the replicate analyses processed from the NIST Standard 2704. The precision and accuracy results were generated by repeating XRF analysis on the same wafer at least five times. All analytes for the filter sample were within the expected range of precision and accuracy.

Table A-1. XRF Data Quality Measurements for Filters

System Analyte Precisiona Precisionb Precisionc Accuracyc
XRF
wt%
Al ±2.4% ±2.3% ±25% ±25%
Si ±1.4% ±5.6% ±25% ±25%
  S ±5.4% ±8.5% ±25% ±25%
  Fe ±1.2% ±1.8% ±25% ±25%
  Ca ±1.6% ±3.6% ±25% ±25%
  K ±0.7% ±N/A ±25% ±N/A
  Ti ±1.0% ±3.7% ±25% ±25%
  Mg ±4.9% ±2.8% ±25% ±25%
           
ppm Cr ±4.7% ±3.9% ±25% ±25%
  Mn ±2.6% ±1.7% ±25% ±25%
  Ni ±19.3% ±10.2% ±25% ±25%
  Cu ±1.8% ±0.4% ±25% ±25%
  Zn ±1.5% ±0.2% ±25% ±25%
  Zr ±9.0% ±3.9% ±25% ±25%
  Sr ±6.8% ±3.9% ±25% ±25%
  Cd ±28.4% ±12.2% ±40% ±40%
  Sb ±37.9% ±9.0% ±40% ±40%
  Sn ±14.6% ±13.9% ±40% ±40%
  Ba ±8.3% ±3.7% ±25% ±25%
  Pb ±2.3% ±1.7% ±25% ±25%

a Relative standard deviation based on replicate analysis of NIST 2704 filter.
b Difference from true value based on replicate analysis of NIST 2704 filter.
c Acceptance/rejection values.


A.2  Total Sample Concentration

Analytical totals for the samples analyzed from the 1997 Lake Pontchartrain survey ranged from approximately 85% to 115%. This range in totals was reflected in the individual elemental concentrations and caused a scatter effect in the final results. When the data was plotted in a metal to metal format that generally show correspondence, there was only scatter showing little to no correlation. The problem of variable total concentration has been solved by normalizing the data to a 90% total. By normalizing the data to 90%, the variation is greatly reduced and the data plots show considerably less scatter. Figure A-1 gives an example of the relationship of Al to Si for the 1997 Lake Pontchartrain data. With the exception of a few samples, the correlation gives a reasonable regression. In addition, mean Al values for normalized 1997 data (6.51 wt%) and for normalized 1996 data (6.89 wt%) are very close. The 1997 Al range was 3.1 to 9.89 wt% as compared to 2.0 to 9.19 wt% for the 1996 data.

While 90% is somewhat arbitrary, it was chosen because the structural H2O was determined to be relatively consistent at 8% to 9%, and elemental Na values were consistently between 0.5% and 2%. The consideration of the structural H2O and Na, along with the remaining analytes should account for >99% of the elemental makeup of the sample.

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Figure A-1. Normalized Al to Si plot for the 1997 Lake Pontchartrain data.

 

A.3  Interlab Sample Comparison

In order to test the quality of the data, six samples from the 1997 Lake Pontchartrain survey were sent to two labs, the XRF lab at Georgia State University (GSU) and the analytical lab at Skidaway Institute of Oceanography (Skidaway). The samples were chosen not because of quality or location, but because of extra sediment collected at these particular stations. The samples were collected during the 1997 survey as bulk sediment slurry samples from the CS³ processor at approximately the same time that the corresponding CS³ filter sample was collected. These samples were dried and archived for future use. Figure A-2 shows the results of the interlab comparison of the six Lake Pontchartrain samples. Five of the samples show a good correlation. One sample, CAIS Sample 244, appeared to be out of line with the other Sample 244s analyzed by GSU and Skidaway. Upon reanalyses, the Al concentration remained the same as previously reported. Since this sample was originally analyzed in 1997, and now in 1998 with the same results, it is mostly likely not a random error on the part of the XRF. Analytical methods, such as, XRF and Atomic Absorption, may not always agree usually reflecting the differences in sample preparation. However, it was shown by Figure A-2 that the data reflects the same relative difference from one method to another.

The GSU samples were processed into fused glass disks and analyzed by a Rigaku 3070 wavelength-dispersive spectrometer utilizing a side-window Rh target X-ray tube (XRF). The sediment was fused using lithium borate flux by heating in a furnace at 1100°C. The ratio of flux to sediment was 9:1, producing a glass disk that was essentially a borate glass with sediment dissolved in it.

The Skidaway samples were processed using a lithium metaborate fusion and analyzed by an atomic absorption spectrophotometer (AA) following EPA Method 7020. Approximately 250 mg of sample was placed in a clean alumina crucible and heated at 900°C for 30 minutes. After cooling, the sample was reweighed and percent loss on ignition was calculated. The ratio of lithium metaborate flux to sample powder is 4:1. A total of 100 mg of ashed sample with 400 mg flux was thoroughly mixed and then placed in a graphite crucible. The crucible was then placed into a muffle furnace at 1050°C for 8 minutes, removed, swirled, and returned to the oven for another 7 minutes. The glass beads from the crucibles were poured directly into a wide-mouth bottle containing 50 ml of 1.5N HNO3 spiked with 10 ppm Ge. The sample was vigorously shaken until all the glass was dissolved. The sample was then analyzed by the AA for Al content.

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Figure A-2. Interlab sample comparison.

 

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