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Appendix E
Field, Sampling, and Data Analysis
Quality Assurance / Quality Control
• Field and Sampling Quality Assurance /
Quality Control Procedures
• Data Analysis Quality Assurance/
Quality Control Procedures
Field and Sampling
Quality Assurance/Quality Control Procedures
Documentation of field activities was completed using a combination of logbooks, field data
records (FDRs), sample tracking systems, and sample custody records. Site and field logbooks
were completed to provide a general record of activities and events that occur during each field
task. FDRs have been designated for each exploration and sample collection task, to provide a
complete record of data obtained during the activity.
Field Logbooks
The field logbooks provided a daily handwritten account of field activities. Logbooks were
hardcover books that were permanently bound. All entries were made in indelible ink, and
corrections were made with a single line with the author initials and date. Each page of the
logbook was dated and initialed by the person completing the log. Partially completed pages
will have a line drawn through the unused portion at the end of each day with the author’s
initials. The following information was generally entered into the field logbooks:
• The date and time of each entry. The daily log generally begins with the Pre-Job Safety
Brief;
• A summary of important tasks or subtasks completed during the day;
• A description of field tests completed in association with the daily task;
• A description of samples collected including documentation of any quality control
samples that were prepared (rinse blanks, duplicates, matrix spike, split samples, etc.);
• Documentation of equipment maintenance and calibration activities;
• Documentation of equipment decontamination activities; and
• Descriptions of deviations from the work plan.
Field Data Records
Sample FDRs contain sample collection and/or exploration details. An FDR was completed
each time a field sample was collected. The goal of the FDR was to document exploration and
sample collection methods, materials, dates and times, and sample locations and identifiers.
Field measurements and observations associated with a given exploration or sample collection
task were recorded on the FDRs. FDRs were maintained throughout the field program in files
that become a permanent record of field program activities.
Sample Identification
In order to ensure that each number for every field sample collected was unique, samples were
identified by the sample location and depth interval, if applicable (e.g., MW-11S (5-6’). Samples
were numbered in accordance with their sample location.
Field Equipment Calibration
Field sampling equipment (e.g., water quality meter) was properly maintained and calibrated
prior to and during continued use to assure that measurements were accurate within the
limitations of the equipment. Personnel will follow the manufacturers’ instructions to determine
if the instruments were functioning within their established operation ranges. The calibration
data was recorded on a FDR.
To be acceptable, a field test must be bracketed between acceptable calibration results.
• The first check may be an initial calibration, but the second check must be a continuing
verification check.
• Each field instrument must be calibrated prior to use.
• Verify the calibration at no more than 24-hour intervals during use and at the end of the
use if the instrument will not be used the next day or time periods greater than 24 hours.
• Initial calibration and verification checks must meet the acceptance criteria
recommended by each instrument manufacturer.
• If an initial calibration or verification check fails to meet the acceptance criteria,
immediately recalibrate the instrument or remove it from service.
• If a calibration check fails to meet the acceptance criteria and it was not possible to
reanalyze the samples, the following actions must be taken:
• Report results between the last acceptable calibration check and the failed calibration
check as estimated (qualified with a “J”);
• Include a narrative of the problem; and
• Shorten the time period between verification checks or repair/replace the instrument.
• If historically generated data demonstrate that a specific instrument remains stable for
extended periods of time, the interval between initial calibration and calibration checks
may be increased.
• Acceptable field data must be bracketed by acceptable checks. Data that was not
bracketed by acceptable checks must be qualified.
• Base the selected time interval on the shortest interval that the instrument maintains
stability.
• If an extended time interval was used and the instrument consistently fails to meet the
final calibration check, then the instrument may require maintenance to repair the
problem or the time period was too long and must be shortened.
• For continuous monitoring equipment, acceptable field data must be bracketed by
acceptable checks or the data must be qualified.
Sampling or field measurement instrument determined to be malfunctioning was repaired or was
replaced with a new piece of equipment.
Sample Custody Requirements
A program of sample custody was followed during sample handling activities in both field and
laboratory operations. This program was designed to assure that each sample was accounted
for at all times. The appropriate sampling and laboratory personnel will complete sample FDRs,
chain-of-custody records, and laboratory receipt sheets.
The primary objective of sample custody procedures was to obtain an accurate written record
that can trace the handling of all samples during the sample collection process, through
analysis, until final disposition.
Field Sample Custody
Sample custody for samples collected during each sampling event was maintained by the
personnel collecting the samples. Each sampler was responsible for documenting each sample
transfer, maintaining sample custody until the samples were shipped off-site, and sample
shipment. The sample custody protocol followed by the sampling personnel involves:
• Documenting procedures and amounts of reagents or supplies (e.g., filters) which
become an integral part of the sample from sample preparation and preservation;
• Recording sample locations, sample bottle identification, and specific sample acquisition
measures on appropriate forms;
• Using sample labels to document all information necessary for effective sample
tracking; and,
• Completing sample FDR forms to establish sample custody in the field before sample
shipment.
Prepared labels were normally developed for each sample prior to sample collection. At a
minimum, each label will contain:
• Sample location and depth (if applicable);
• Date and time collected;
• Sampler identification; and,
• Analyses requested and applicable preservative.
A manually-prepared chain-of-custody record was initiated at the time of sample collection. The
chain-of-custody record documents:
• Sample handling procedures including sample location, sample number, and number of
containers corresponding to each sample number;
• The requested analysis and applicable preservative;
• The dates and times of sample collection;
• The names of the sampler(s) and the person shipping the samples (if applicable);
• The date and time that samples were delivered for shipping (if applicable);
• Shipping information (e.g., FedEx Air Bill); and,
• The names of those responsible for receiving the samples at the laboratory.
Chain-of-custody records were prepared by the individual field samplers.
Sample Container Packing
Sample containers were packed in plastic coolers for shipment or pick up by the laboratory.
Bottles were packed tightly to reduce movement of bottles during transport. Ice was placed in
the cooler along with the chain-of-custody record in a separate, resealable, air tight, plastic bag.
A temperature blank provided by the laboratory will also be placed in each cooler prior to
shipment if required for the type of samples collected and analyses requested.
Quality Assurance and Quality Control Samples
The following Quality Assurance/Quality Control samples were collected during the proposed
field activities:
• Equipment rinse blanks (one per day or one per 20 samples);
• Field Duplicates (one per 20 samples for field and lab duplicates)
Equipment rinse blanks were collected from non-dedicated equipment used between wells and
from drilling equipment between soil samples. The field equipment was cleaned following
documented cleaning procedures. An aliquot of the final control rinse water was passed over
the cleaned equipment directly into a sample container and submitted for analysis. The
equipment rinse blanks enable evaluation of bias (systematic errors) that could occur due to
decontamination.
A field duplicate was a replicate sample prepared at the sampling locations from equal portions
of all sample aliquots combined to make the sample. Both the field duplicate and the sample
were collected at the same time, in the same container type, preserved in the same way, and
analyzed by the same laboratory as a measure of sampling and analytical precision.
Field QA/QC samples were analyzed for the same constituents as proposed for the soil and
groundwater samples.
Decontamination Procedures
Decontamination Pad
A decontamination pad was constructed for field cleaning of drilling equipment. The
decontamination pad will meet the following requirements:
• The pad was constructed in an area believed to be free of surface contamination.
• The pad was lined with a water-impermeable material with no seams within the pad.
The material should be easily replaced (disposable) or repairable.
• If possible, the pad was constructed on a level, paved surface to facilitate the removal of
decontamination water. This may be accomplished by either constructing the pad with
one corner lower than the rest, or by creating a lined sump or pit in one corner.
• Sawhorses or racks constructed to hold field equipment while being cleaned were high
enough above ground to prevent equipment from being contacted by splashback during
decontamination.
Decontamination water was allowed to percolate into the ground adjacent to the
decontamination pad. Containment and disposal of decontamination water was not required.
At the completion of field activities, the decontamination pad was removed and any sump or pit
was backfilled with appropriate material.
Decontamination of Field Sampling Equipment
Field sampling equipment was decontaminated between sample locations using potable water
and phosphate-and-borax-free detergent solution and a brush, if necessary, to remove
particulate matter and surface films. Equipment will then be rinsed thoroughly with tap water to
remove detergent solution prior to use at the next sample location.
Decontamination of Drilling Equipment
Any downhole drilling equipment was steam cleaned between boreholes. The following
procedure was used for field cleaning augers, drill stems, rods, tools, and associated downhole
equipment.
• Hollow-stem augers, bits, drilling rods, split-spoon samplers and other downhole
equipment was placed on racks or sawhorses at least two feet above the floor of the
temporary decontamination pad. Soil, mud, and other material were removed by hand,
brushes, and potable water. The equipment was steam cleaned using a high pressure,
high temperature steam cleaner.
• Downhole equipment was rinsed thoroughly with potable water after steam cleaning.
The clean equipment will then be removed from the decontamination pad and either placed on
the drill rig, if mobilizing immediately to the next boring, or placed on and covered with clean,
unused plastic sheeting if not used immediately.
Data Analysis
Quality Assurance/Quality Control Procedures
Duke Energy – Dan River Speciation Page 1 of 3
DAN RIVER
DATA VALIDATION AND USABILITY REPORT
(SPECIATION)
HEXAVALENT CHROMIUM in WATER by BRL IC-ICP-DRC-MS
ARSENIC SPECIATION in WATER by BRL IC-ICP-CRC-MS
SELENIUM SPECIATION in WATER by BRL IC-ICP-CRC-MS
IRON SPECIATION in WATER by BRL IC-ICP-CRC-MS and FERROUS IRON by the
FERROZINE PROCEDURE
MANGANESE SPECIATION in WATER by BRL IC-ICP-CRC-MS
Project: Duke Energy: Dan River Site Investigation
Project/Task Number: 392-246418
Sample Data Package: J15060723, J15060893, J15060897, J15070090, J15070099,
J15070100, J15070130, J15070273
Laboratory: Brooks Rand Laboratory, Bothell, WA
Sample Matrix: Equipment and Pump Blanks (Aqueous)
Sampling Dates: 18 June through 1 July 2015
Validation Guidelines: Project Work Plan (Proposed Groundwater Assessment Work Plan
(Rev.1) [HDR, December 2014]), United States Environmental
Protection Agency (USEPA) Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods, 3rd edition (SW-846), National
Functional Guidelines for Inorganic Data Review, EPA-540-R-013-
001 [EPA, August 2014], and professional judgment
Validation Level: Steps I (verification), IIa (validation) and III (data usability)
Data Reviewer: Todd Wilson, Al Vetrovs, Hailey Fitterer, Ian Welch, Steve Nyman
HDR
SUMMARY
Laboratory data were acceptable with qualification as noted below. Completeness was greater
than 95%, which met the goal of 90% for the project.
I. SAMPLE RECEIPT / CHAIN OF CUSTODY
Samples were received generally within a temperature of -1-6 oC. Minimal qualification was
required.
II. HOLDING TIMES
All holding time criteria were met and a number of qualifications were required for the ferrous iron
and hexavalent chromium analyses. Samples were qualified as J- or UJ due to missed holding
times.
III. SAMPLES ANALYZED
All planned samples were collected and all scheduled analyses were performed. The correct
analyte lists were reported. No qualification was required.
IV. BLANKS
METHOD (PREPARATION) BLANKS
Target analytes were generally not detected in method blanks except as discussed below.
Duke Energy – Dan River Speciation Page 2 of 3
Chromium (VI): Chromium generally contained low level detections. Qualification as blank
contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
Arsenic (III and VI): Arsenic was generally non-detect in the method blanks. Qualification as blank
contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
Selenium (IV and VI): Selenium was generally non-detect in the method blanks. Qualification as
blank contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
Iron (II and III): Iron was generally non-detect in the method blanks. Qualification as blank
contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
Manganese (II and IV): Manganese (total and dissolved) was generally detected in the method
(preparation) blanks. Qualification as blank contamination was provided as UJ or J+, unless the
result was greater than 10 x the blank concentration.
INITIAL AND CONTINUING CALIBRATION BLANKS
The ICB and CCB information was not provided by the laboratory as a Level II data package. The
text within each of the data package indicated the ICB and CCB were within acceptable criteria.
Chromium (VI): Initial and Continuing Calibration Blanks were acceptable. No qualification was
required.
Arsenic (III and VI): Initial and Continuing Calibration Blanks were acceptable. No qualification
was required.
Selenium (IV and VI): Initial and Continuing Calibration Blanks were acceptable. No qualification
was required.
Iron (II and III): Initial and Continuing Calibration Blanks were acceptable. No qualification was
required.
Manganese (II and IV): Initial and Continuing Calibration Blanks were acceptable. No qualification
was required.
EQUIPMENT (PUMP) BLANKS
Target analytes were detected in the equipment and pump blanks (EB or PB).
All Analyses: A number of the EBs contained detections of metals. Concentrations of the detected
metals were not qualified if less than 10 times concentrations detected in the soil results. If the
results were less than 10 times the blank concentration, data were qualified as UJ or J+.
V. LABORATORY CONTROL SAMPLES (LCS)
Recoveries and relative percent differences (RPDs) were generally within the laboratory’s
control limits. If the LCS was outside of the acceptable criteria of 75-125% recovery the data
were qualified. Data were qualified as J- if the LCS recovery was less than 75% and J+ if the LCS
recovery was greater than 125%.
Duke Energy – Dan River Speciation Page 3 of 3
V. INITIAL CALIBRATION VERIFICATION SAMPLES (ICV)
Brooks Rand Lab provided a combination of ICV and Certified Reference Materials to provide
an indication of compliance. In general, the ICV and Certified Reference Materials were within
acceptable criteria. Data were qualified as J- if the LCS recovery was less than 90% and J+ if
the LCS recovery was greater than 110%.
VI. MATRIX SPIKE / MATRIX SPIKE DUPLICATE (MS/MSD)
A sample was not designated on the COCs for MS/MSD analysis. An MS/MSD was analyzed
on every batch. If a site-specific MS/MSD sample was completed, a comparison of the RPDs
was completed. If a site-specific sample was not available, the MS/MSD was not evaluated.
VIII. FIELD DUPLICATES
Field duplicates were designated, but in some instances the sample pair could not be
determined based on the naming convention used in the field (fictitious name, DUP-X, Date-
Duplicate, etc.). If a field duplicate could be determined, the RPDs were calculated and
comparability between the field and duplicate samples completed. If the RPD was greater than
20% RPD, the field and duplicate analytes were qualified as J.
IX. LABORATORY (MATRIX) DUPLICATES
Laboratory duplicate (LD) analyses were performed on the samples and were generally within
acceptable criteria, and minimal qualification was required.
X. INSTRUMENT CALIBRATION
Instrument calibrations were not provided; however, the laboratory indicated the calibrations were
within acceptable criteria and requirements were met. No qualification was required.
XII. SAMPLE REPORTING LIMITS
All RLs were at or below either the regulatory criteria for human health criteria. The RLs were
generally at or below the ecological criteria, if available for metals speciation.
XIII. SAMPLE RESULTS / TRANSCRIPTION VERIFICATION
Transcription between the data package and the EDDs was verified. Results reported between
the MDLs and RLs were qualified as estimated (J).
Duke Energy – Dan River Water Page 1 of 4
DAN RIVER
DATA VALIDATION AND USABILITY REPORT
(SEEP/GROUNDATER/SURFACE WATER)
TOTAL AND DISSOLVED METALS in WATER by USEPA Method 200.7/200.8
TOTAL AND DISSOLVED MERCURY in WATER by USEPA Method 245.1
LOW-LEVEL MERCURY BY USEPA Method 1631E
NITROGEN/NITRATE + NITRITE by USEPA Method 353.2
SULFIDE by Standard Method 4500-S2D
TOTAL ORGANIC CONTENT by Standard Method 5310B
METHANE by USEPA RSK SOP-175
SULFATE, CHLORIDE, and NITRATE as N by EPA Method 300.0
ALKALINITY/BICARBONATE and CARBONATE by Standard Method 2320B
TOTAL SUSPENDED SOLIDS by Standard Method 2540D
TOTAL DISSOLVED SOLIDS by Standard Method 2540C
Project: Duke Energy: Dan River Site Investigation
Project/Task Number: 392-246418
Sample Data Package: J15050761, J15060083, J15060152, J15060207, J15060251,
J15060338, J15060369, J15060372, J15060434, J15060566,
J15060580, J15060630, J15060664, J15060739, J15060742,
J15060745, J15060747, J15060749, J15060752, J15060813,
J15060815, J15060816, J15060817, J15060857, J15060859,
J15060910, J15060911, J15060913, J15060958, J15060968,
J15070016, J15070018, J15070020, J15070062, J15070065,
J15070088
Laboratory: PACE Laboratories (Asheville, Green Bay, Minneapolis, Ormond
Beach), Shealy Environmental Services, West Columbia, South
Carolina, and Element One, Huntersville, North Carolina
Sample Matrix: Equipment and Filter Blanks (Aqueous)
Sampling Dates: 27 May through 1 July 2015
Validation Guidelines: Project Work Plan (Proposed Groundwater Assessment Work Plan
(Rev.1) [HDR, December 2014]), United States Environmental
Protection Agency (USEPA) Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods, 3rd edition (SW-846), National
Functional Guidelines for Inorganic Data Review, EPA-540-R-013-
001 [EPA, August 2014], and professional judgment
Validation Level: Steps I (verification), IIa (validation) and III (data usability)
Data Reviewer: Todd Wilson, Al Vetrovs, Hailey Fitterer, Ian Welch, Craig Osborn
HDR
SUMMARY
Laboratory data were acceptable with qualification as noted below. Completeness was greater
than 95%, which met the goal of 90% for the project.
I. SAMPLE RECEIPT / CHAIN OF CUSTODY
Samples were received generally within a temperature of 0-6 oC. Minimal qualification was
required.
Duke Energy – Dan River Water Page 2 of 4
II. HOLDING TIMES
All holding time criteria were met and minimal qualification was required, except for nitrate
samples. All of the samples were qualified as J- or UJ due to missed holding times.
III. SAMPLES ANALYZED
All planned samples were collected and all scheduled analyses were performed. The correct
analyte lists were reported. No qualification was required.
IV. BLANKS
METHOD BLANKS
Target analytes were generally not detected in method blanks except as discussed below.
Total and Dissolved Metals (including Mercury): Method blanks were generally non-detect for the
metals of interest. Qualification as blank contamination was provided as UJ or J+, unless the result
was greater than 10 x the blank concentration.
Nitrogen, Nitrate, Sulfate, and Chloride: Nitrate, sulfate and chloride were generally non-detect in
the method blanks. Qualification as blank contamination was provided as UJ or J+, unless the
result was greater than 10 x the blank concentration.
Total Organic Carbon: Total Organic Carbon (TOC) was generally non-detect in the method
blanks. No qualification was required.
Methane: Methane was generally non-detect in the method blanks. Qualification as blank
contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
Sulfide: Sulfide was generally non-detect in the method blanks. Qualification as blank
contamination was provided as UJ or J+, unless the result was greater than 10 x the blank
concentration.
TDS/TSS and Alkalinity: These methods were generally non-detect in the method blanks.
Qualification as blank contamination was provided as UJ or J+, unless the result was greater than
10 x the blank concentration.
INITIAL AND CONTINUING CALIBRATION BLANKS
The ICB and CCB information was not provided by the laboratory as a Level II data package. The
text within each of the data package indicated if the ICB and CCB was within acceptable criteria.
Total and Dissolved Metals: Initial and Continuing Calibration Blanks were acceptable. No
qualification was required.
Nitrogen, Nitrate, Sulfate, and Chloride: Initial and Continuing Calibration Blanks were acceptable.
No qualification was required.
Total Organic Carbon: Initial and Continuing Calibration Blanks were acceptable. No qualification
was required.
Methane: Initial and Continuing Calibration Blanks were acceptable. No qualification was required.
Sulfide: Initial and Continuing Calibration Blanks were acceptable. No qualification was required.
Duke Energy – Dan River Water Page 3 of 4
TDS/TSS and Alkalinity: Initial and Continuing Calibration Blanks were acceptable. No
qualification was required.
EQUIPMENT BLANKS
Target analytes were detected in the equipment blanks (EB).
Total Metals: A number of the EBs contained detections of metals. Concentrations of the detected
metals were not qualified if less than 10 times concentrations detected in the soil results. If the
results were less than 10 times the blank concentration, data were qualified as UJ or J+.
V. LABORATORY CONTROL SAMPLES (LCS)
Recoveries and relative percent differences (RPDs) were generally within the laboratory’s
control limits. If the LCS was outside of the acceptable criteria of 75-125% recovery the data
were qualified. Data were qualified as J- if the LCS recovery was less than 75% and J+ if the LCS
recovery was greater than 125%.
VI. MATRIX SPIKE / MATRIX SPIKE DUPLICATE (MS/MSD)
A sample was not designated on the COCs for MS/MSD analysis. An MS/MSD was analyzed
on every batch. If a site-specific MS/MSD sample was completed, a comparison of the RPDs
was completed. If a site-specific sample was not available, the MS/MSD was not evaluated.
Total and Dissolved Metals: Samples were diluted due to interferences with the ICPMS method
for all associated metals and samples up to 100X. Non-detect values may be diluted. The
recoveries of total and dissolved metals were generally acceptable, and limited qualification of
data was required.
Nitrogen, Nitrate, Sulfate, and Chloride: The recoveries of nitrate, sulfate and chloride were
generally acceptable, and minimal qualification of data was required.
Total Organic Carbon: The recoveries of TOC were generally acceptable, and minimal
qualification of data was required.
Methane: The recoveries of Methane were generally acceptable, and minimal qualification of data
was required.
Sulfide: The recoveries of sulfide were generally acceptable, and minimal qualification of data was
required.
TDS/TSS and Alkalinity: The recoveries of TOC were generally acceptable, and minimal
qualification of data was required.
VIII. FIELD DUPLICATES
Field duplicates were designated, but in some instances the sample pair could not be
determined based on the naming convention used in the field (fictitious name, DUP-X, Date-
Duplicate, etc.). If a field duplicate could be determined, the RPDs were calculated and
comparability between the field and duplicate samples completed. If the RPD was greater than
20% RPD, the field and duplicate analytes were qualified as J.
IX. LABORATORY DUPLICATES
Laboratory duplicate (LD) analyses were performed on the chloride, sulfate, nitrate, and pH
samples and were generally within criteria, and minimal qualification was required.
Duke Energy – Dan River Water Page 4 of 4
X. INSTRUMENT CALIBRATION
Instrument calibrations were not provided; however, the laboratory indicated the calibrations were
within acceptable critieria and requirements were met. No qualification was required.
XII. SAMPLE REPORTING LIMITS
All RLs were at or below either the regulatory criteria for human health criteria. The RLs were
generally at or below the ecological criteria.
XIII. SAMPLE RESULTS / TRANSCRIPTION VERIFICATION
Transcription between the data package and the EDDs was verified. Results reported between
the MDLs and RLs were qualified as estimated (J).
Duke Energy – Dan River Radiological Page 1 of 2
DATA VALIDATION AND USABILITY REPORT
U233, U234, U236 and U238 by USEPA SW-846 Method 6020A
Ra-226 by USEPA Method 903.1 Modified
Ra-228 by USEPA Method 904.0/SW-846 Method 9320 Modified
Project: Duke Energy Dan River Radiological
Project/Task Number: 392-246415-001
Sample Data Package: J15060861, J15060949, J15060992, J15060993, J15060997,
J15070051
Laboratory: GEL Laboratories, LLC (Charleston, SC)
Sample Matrix: Groundwater (Aqueous)
Sampling Dates: 23-30 June 2015
Validation Guidelines: Project Work Plan (Proposed Groundwater Assessment Work Plan
(Rev.1) [HDR, December 2014]), United States Environmental
Protection Agency (USEPA) Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods, 3rd edition (SW-846), Method
903.1, Method 904.4, National Functional Guidelines for Inorganic
Data Review, EPA-540-R-013-001 [EPA, August 2014], and
professional judgment
Validation Level: Stage 2A
Data Reviewer: Lynn K. Lutz, HDR
SUMMARY
Laboratory data were acceptable with qualification as noted below. No data were rejected.
Completeness was 100%.
I. SAMPLE RECEIPT / CHAIN OF CUSTODY
Samples were received at 1°C, 5°C, 21°C and 23°C. These are acceptable temperatures for
metals. Methods 903.1 and 904.0 state that no sample icing is required. No qualification was
required.
II. HOLDING TIMES
All holding time criteria of less than 180 days were met and no qualification was required.
III. SAMPLES ANALYZED
All planned samples were collected and all scheduled analyses were performed. The correct
analyte lists were reported. No qualification was required.
IV. BLANKS
METHOD BLANKS
Target analytes were not detected in the method blanks and no qualification was required.
EQUIPMENT BLANKS
There were no equipment blanks associated with these samples and no qualification was
required.
V. LABORATORY CONTROL SAMPLES (LCS)
Recoveries and relative percent differences (RPDs) were within the laboratory’s control limits.
Qualification was not required.
Duke Energy – Dan River Radiological Page 2 of 2
VI. MATRIX SPIKE / MATRIX SPIKE DUPLICATE (MS/MSD)
Some project samples were spiked for MS/MSD analysis. Recoveries and RPDs were within
control limits and no qualification was required.
VII. FIELD DUPLICATES
A field duplicate (FD) sample of MW-11 was collected as MW-11Dup. Control limits of 20% RPD,
or less than the MRL for results less than five times the MRL, as suggested in the Functional
Guidelines, were used. All results were within the control limits and no qualification was required.
VIII. LABORATORY DUPLICATES
Laboratory duplicate (LD) analyses were performed on some samples from this project. Control
limits of 20% RPD, or less than the MRL for results less than five times the MRL, as suggested
in the Functional Guidelines, were met and no qualification was required except as noted below.
U238: The RPD between the parent sample MW-11DUP and its LD was 67%, above the control
limit, and this result has been qualified as estimated with a possible low bias (J-), as the
reported value was the lower of the two.
IX. INSTRUMENT CALIBRATION
Instrument calibration information was not assessed, as it was not included in the data packages.
X. SAMPLE RESULTS / TRANSCRIPTION VERIFICATION
Transcription between the data package and the EDDs was verified. Results reported between
the MDLs and RLs were qualified as estimated (J).
Duke Energy – Dan River Sediments Page 1 of 2
DATA VALIDATION AND USABILITY REPORT
TOTAL METALS by USEPA SW-846 Method 6010/6020/7471
CHLORIDE, NITRATE as N, SULFATE by USEPA SW-846 Method 9056
TOTAL ORGANIC CONTENT by USEPA SW-846 Method 9060
pH by USEPA SW-846 Method 9045
CATION EXCHANGE CAPACITY (CEC) by USEPA SW-846 Method 9081
OXIDATION-REDUCATION POTENTIAL (ORP) by METHOD G200-9
Project: Duke Energy Dan River Sediments
Project/Task Number: 392-246415-001
Sample Data Package: J15050764, J15070108, J15070112, J15070641
Laboratory: Access Analytical, Inc. (Atlanta, GA) (CEC, ORP)
PACE Laboratories (Asheville, Green Bay, Ormond Beach)
Sample Matrix: Sediment
Sampling Dates: 27 May, 30 June and 16 July 2015
Validation Guidelines: Project Work Plan (Proposed Groundwater Assessment Work Plan
(Rev.1) [HDR, December 2014]), United States Environmental
Protection Agency (USEPA) Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods, 3rd edition (SW-846), National
Functional Guidelines for Inorganic Data Review, EPA-540-R-013-
001 [EPA, August 2014], and professional judgment
Validation Level: Stage 2A (CEC and ORP Stage 1)
Data Reviewer: Todd Wilson and Lynn K. Lutz, HDR
SUMMARY
Laboratory data were acceptable with qualification as noted below. No data were rejected.
Completeness was 100%.
I. SAMPLE RECEIPT / CHAIN OF CUSTODY
Samples were received at the correct temperature (between 0°C and 6°C). No qualification was
required.
II. HOLDING TIMES
All holding time criteria were met and no qualification was required, except for all samples for ORP
and nitrate as N; these sample results were qualified as J, J- or UJ due to missed holding times.
III. SAMPLES ANALYZED
All planned samples were collected and all scheduled analyses were performed. The correct
analyte lists were reported. No qualification was required.
IV. BLANKS
METHOD BLANKS
Target analytes were not detected in method blanks and no qualification was required.
EQUIPMENT BLANKS
Equipment blanks were not collected and no qualification was required.
V. LABORATORY CONTROL SAMPLES (LCS)
Duke Energy – Dan River Sediments Page 2 of 2
Recoveries and relative percent differences (RPDs) were within the laboratory’s control limits
and no qualification was required except as noted below.
Mercury: The LCS recovery of mercury at 133% was above the control limits. Mercury was
detected in both samples and was qualified as estimated with a possible high bias (J+).
VI. MATRIX SPIKE / MATRIX SPIKE DUPLICATE (MS/MSD)
Some project samples were spiked for MS/MSD analysis. Recoveries and RPDs were generally
within control limits and no qualification was required except as noted below.
Nitrate as N: The recoveries of nitrate in samples S-2 and S-3 were below the control limits. Nitrate
was not detected in both samples and was qualified as non-detect estimated (UJ)
The recoveries of chloride and nitrate in sample SW-3 were below control limits, and these non-
detect results have been qualified as non-detect estimated (UJ) in the parent sample.
VII. FIELD DUPLICATES
Field duplicate (FD) samples were not collected and no qualification was required.
VIII. LABORATORY DUPLICATES
Laboratory duplicate (LD) analyses were performed on some samples from this project. Control
limits of 20% RPD, or less than the MRL for results less than five times the MRL, as suggested
in the Functional Guidelines, were met and no qualification was required.
IX. INSTRUMENT CALIBRATION
Instrument calibration requirements were met, according to the case narrative. No qualification was
required.
X. SAMPLE REPORTING LIMITS
Most RLs were at or below the regulatory criteria (soil RSLs) for human health and the
ecological criteria (soil ESVs) except as noted in the table below. When an MDL is above the
regulatory criterion, results reported as non-detect cannot be assured to be below the criterion.
Analyte RL (mg/Kg) MDL (mg/Kg) RSL (mg/Kg) ESV (mg/Kg)
Antimony 8.5 4.3 ok 3.5
Arsenic 8.5 4.3 3.0 ok
Boron 21 10.7 ok 0.50
Chromium 2.1 1.1 ok 0.40
Molybdenum 4.3 2.1 ok 2.0
Selenium 8.5 4.3 ok 0.81
Thallium 8.5 4.3 1.2 1.0
Vanadium 8.5 4.3 ok 2.0
XI. SAMPLE RESULTS / TRANSCRIPTION VERIFICATION
Transcription between the data package and the EDDs was verified. Results reported between
the MDLs and RLs were qualified as estimated (J).
Duke Energy – Dan River Soil and Ash Page 1 of 7
DATA VALIDATION AND USABILITY REPORT
TOTAL METALS by USEPA SW-846 Method 6010/6020/6020A/7470A/7471
CHLORIDE, NITRATE as N, SULFATE by USEPA SW-846 Method 9056
TOTAL ORGANIC CARBON by USEPA SW-846 Method 9060
pH by USEPA SW-846 Method 9045
CHLORIDE by STANDARD METHOD SM4500-Cl-E (SPLP)
NITRATE NITROGEN by USEPA Method 353.2 (SPLP)
SULFATE by USEPA Method 300.0 (SPLP)
Project: Duke Energy Dan River Soil and Ash
Project/Task Number: 392-246415-001
Sample Data Package: J15030688, J15040062, J15040306, J15040619, J15050050,
J15050287, J15050569, J15050662, J15050764, J15060079,
J15060274, J15060635, J15060944, J15060950, J15070112
Laboratory: PACE Laboratories (Asheville, Green Bay, Minneapolis, Ormond
Beach)
Sample Matrix: Soil, Ash, Ash by SPLP, and Equipment Blanks (Aqueous)
Sampling Dates: 21 March to 30 June 2015
Validation Guidelines: Project Work Plan (Proposed Groundwater Assessment Work Plan
(Rev.1) [HDR, December 2014]), United States Environmental
Protection Agency (USEPA) Test Methods for Evaluating Solid
Waste, Physical/Chemical Methods, 3rd edition (SW-846), National
Functional Guidelines for Inorganic Data Review, EPA-540-R-013-
001 [EPA, August 2014], and professional judgment
Validation Level: Stage 2A
Data Reviewer: Todd Wickert, Hailey Fitterer and Lynn K. Lutz, HDR
SUMMARY
Laboratory data were acceptable with qualification as noted below. Antimony and selenium in
sample BG-5D(1-2) had very low (less than 10%) MS/MSD recoveries and these results in this
sample were qualified as rejected (R). No other data were rejected. Completeness was 100%
except for antimony and selenium; due to the large number of samples in this project,
completeness for these analytes was essentially 100%.
I. SAMPLE RECEIPT / CHAIN OF CUSTODY
Samples were received at the correct temperature (between 0°C and 6°C). No qualification was
required.
II. HOLDING TIMES
All holding time criteria were met and no qualification was required except as noted below.
Mercury: Mercury in sample DUP-1 collected on 4/13/2015 was analyzed 19 days past the 28 day
holding time, and this result has been qualified as estimated with a possible low bias (J-).
Mercury in sample AS-2D(3-5) was analyzed one day past the 28 day holding time, and this result
has been qualified as non-detect estimated (UJ).
Mercury in the SPLP analysis of sample AB-25BR(0-2) was analyzed two days past the 28 day
holding time, and this result has been qualified as estimated with a possible low bias (J-).
Duke Energy – Dan River Soil and Ash Page 2 of 7
Anions: All nitrate as N in soil and some nitrate nitrogen in aqueous samples were analyzed past
their 48 hour holding time, and these sample results were qualified as estimated with a possible
low bias (J-) or non-detect estimated (UJ).
Chloride and sulfate in sample DUP-1 collected on 4/13/2015 was analyzed 11 days past the 28
day holding time, and these results have been qualified as non-detect estimated (UJ).
TOC: TOC in sample Duplicate (4/28/15) was analyzed two days past the 28 day holding time, and
this result has been qualified as estimated with a possible low bias (J-).
pH: All samples for pH in soil were analyzed past the holding time and these sample results were
qualified as estimated (J)., except for, all nitrate as N in soil, and some nitrate nitrogen in aqueous
samples; these sample results were qualified as J, J- or UJ due to missed holding times.
III. SAMPLES ANALYZED
All planned samples were collected and all scheduled analyses were performed. The correct
analyte lists were reported. No qualification was required.
IV. BLANKS
METHOD BLANKS
Target analytes were generally not detected in method blanks (MB) except as noted below.
Metals: Copper and lead in three equipment blanks (collected 4/29/2015, 4/30/2015 and 5/1/2015)
was detected at less than 10 times the MB concentration, and these results have been qualified as
estimated with a possible high bias (J+).
SPLP Metals: Sodium in the SPLP analysis of sample AB1D (24.0-26.0) was detected at less than
10 times the MB concentration, and this result has been qualified as estimated with a possible high
bias (J+).
Lead in the SPLP analysis of sample MW-318BR(19-20) was detected at less than 10 times the
MB concentration, and this result has been qualified as estimated with a possible high bias (J+).
Mercury in the SPLP analysis of sample AB-35BR(18-19.5) was detected at less than 10 times the
MB concentration, and this result has been qualified as estimated with a possible high bias (J+).
SPLP Anions: Sulfate in the SPLP analysis of several samples was detected at less than 10 times
the MB concentration, and these results have been qualified as estimated with a possible high bias
(J+). The samples were:
AB15D (24.0-26.0) MW-306BR(70-71.5) MW-318BR(19-20)
AB-25BR(0-2) MW-314BR(30-31.5) MW-301BR(3-4)
AB-10D(20-21.5) AB-35BR(18-19.5) AB-35BR(20-21.5)
Nitrate nitrogen in the SPLP analysis of samples MW-301BR(3-4) and AB-25BR(0-2) was detected
at less than 10 times the MB concentration, and these results have been qualified as estimated
with a possible high bias (J+).
EQUIPMENT BLANKS
Target analytes were generally not detected in equipment (rinsate) blanks (EB) except as noted
below.
Duke Energy – Dan River Soil and Ash Page 3 of 7
Metals: Metals in several samples were detected at less than 10 times the MB concentration, and
these results have been qualified as estimated with a possible high bias (J+). The samples and
metals were:
MW-301BR(3-4) Zinc MW-310BR(10-11.5) Calcium
MW-301BR(5-7) Zinc MW-317BR(10-11) Calcium
MW-301BR(15-16) Zinc MW-317BR(15-16) Sodium
MW-301BR(30-31) Zinc GWA-8D(5-10) Calcium
MW-306BR(55-56.5) Zinc GWA-8D(15-20) Sodium
MW-306BR(40-41.5) Zinc AB-5D(20-21.5) Boron
MW-306BR(70-71.5) Zinc AB-5D(25-26.5) Boron
GWA-12D(10-11.5) Sodium GWA-9D(55-56.5) Boron
GWA-12D(20-21) Sodium GWA-9D(20-21.5) Calcium
MW315BR(3.0-4.5) Sodium GWA-9D(30-31.5) Calcium
MW315BR(21-22.5) Sodium AB-10D(30-31.5) Boron
GWA-12D(15-15.2) Sodium DUP-4 (4/12/2015) Boron
SPLP Metals: Several metals in the SPLP analysis of several samples were detected at less than
10 times the MB concentration, and these results have been qualified as estimated with a possible
high bias (J+). The samples and metals were:
MW-301BR(3-4)
Chromium
Copper
Iron
Lead
Manganese
Molybdenum
Nickel
Zinc
MW-306BR(70-71.5) Molybdenum
Zinc
MW-318BR(19-20)
Aluminum
Chromium
Lead
Manganese
Nickel
Potassium
MW-314BR(30-31.5)
Boron
Copper
Lead
Manganese
Potassium
Anions: Sulfate in MW-314BR(30-31.5) and AB-10D(20-21.5) was detected at less than 10 times
the MB concentration, and these results have been qualified as estimated with a possible high bias
(J+).
V. LABORATORY CONTROL SAMPLES (LCS)
Recoveries and relative percent differences (RPDs) were within the laboratory’s control limits
and no qualification was required except as noted below.
Duke Energy – Dan River Soil and Ash Page 4 of 7
Metals: Cadmium recovery was below control limits in one LCS, and cadmium in the associated
samples was non-detect and qualified as non-detect estimated (UJ). The samples were:
GWA-1D(30-31.5) GWA-2D(24-25) MW-314BR(10-11.5)
GWA-1D(40-40.5) GWA-2D(49-50) MW-314BR(20-21.5)
AB-5D(20-21.5) GWA-9D(20-21.5) MW-314BR(30-31.5)
AB-5D(25-26.5) GWA-9D(30-31.5) MW-314BR(40-41.5)
AB-5D(30-31.5) GWA-9D(40-41.5) MW-314BR(45.0-50.45)
GWA-1D(102-104) GWA-9D(55-56.5)
GWA-2D(19-20) AB-10D(30-31.5)
VI. MATRIX SPIKE / MATRIX SPIKE DUPLICATE (MS/MSD)
Recoveries and relative percent differences (RPDs) were within the laboratory’s control limits
and no qualification was required except as noted below. Only parent samples were qualified.
the
Sample ID Analyte Recoveries High or
Low?
Qualifier
GWA-11D(10-11.5) Molybdenum Low UJ
GWA-11D(25-26.5) Antimony
Arsenic
Selenium
Low
Low
Low
UJ
J-
J-
AS-4D(11-12.5) Mercury Low J-
GWA-1D(30-31.5) Antimony
Arsenic
Barium
Chloride
Sulfate
Low
Low
Low
Low
Low
UJ
J-
J-
UJ
UJ
MW-301BR(3-4) Chloride
Sulfate
Low
Low
UJ
UJ
MW-301BR(30-31) Beryllium
Calcium
Mercury
Nickel
Zinc
Low
High
Low
Low
Low
J-
J+
J-
J-
J-
MW-306BR(55-56.5) Antimony
Cobalt
Thallium
Low
High
Low
UJ
J+
UJ
MW-303BR(90-91.5) Antimony
Beryllium
Cadmium
Cobalt
Molybdenum
Nickel
Selenium
Strontium
Low
Low
Low
High
Low
High
Low
Low
UJ
J-
UJ
J+
UJ
J+
J-
J-
DUP-1 (collected
4/13/2015)
Antimony
Arsenic
Barium
Boron
Cadmium
Chloride
Chromium
Low (<10%)
Low
High
Low
Low
Low
High
R
J-
J+
UJ
UJ
UJ
J+
Duke Energy – Dan River Soil and Ash Page 5 of 7
Sample ID Analyte Recoveries High or
Low?
Qualifier
Copper
Manganese
Molybdenum
Selenium
Thallium
High
High
Low
Low
Low
J+
J+
UJ
J-
UJ
SB-3(1-2) Antimony
Arsenic
Cobalt
Magnesium
Molybdenum
Low
Low
Low
Low
Low
UJ
J-
J-
J-
UJ
SB-3(10-11) TOC High J+
MW-310BR(25-26.5) Antimony
Arsenic
Molybdenum
Potassium
Selenium
Strontium
Low
Low
Low
Low
Low
Low
UJ
J-
UJ
J-
J-
J-
MW-317BR(15-16) Antimony
Arsenic
Boron
Chloride
Selenium
Low
Low
Low
Low
Low
UJ
UJ
J-
UJ
J-
SB-1(25-26.5) Chloride
Sulfate
Low
Low
UJ
J-
GWA-1D(30-31.5) Antimony
Arsenic
Barium
Chloride
Sulfate
Low
Low
Low
Low
Low
UJ
J-
J-
UJ
UJ
BG-1D(2) Antimony
Arsenic
Barium
Cobalt
Lead
Magnesium
Thallium
Low
Low
High
High
High
High
Low
UJ
UJ
J+
J+
J+
J+
UJ
BG-5D(1-2) Antimony
Arsenic
Barium
Boron
Cadmium
Chromium
Cobalt
Selenium
Thallium
Low (<10%)
Low
High
Low
Low
Low
Low
Low (<10%)
Low
R
J-
J+
UJ
UJ
J-
J-
R
UJ
AS-2D(3-5) Antimony
Arsenic
Cadmium
Nickel
Selenium
Low
Low
Low
High
Low
UJ
UJ
UJ
J+
J-
Duke Energy – Dan River Soil and Ash Page 6 of 7
Sample ID Analyte Recoveries High or
Low?
Qualifier
AB15D (26.0-26.5) TOC Low J-
AB-25BR(0-2) SPLP Strontium (SPLP) High J+
EB(5/30/15) Aluminum High J+
RINSATE-20150512 Boron Low J-
EB(5/06/15) Aluminum
Calcium
High
High
J+
J+
EB(5/05/15)
EB(5/07/15)
EB(5/09/15)
Aluminum
Calcium
Iron
High
High
High
J+
J+
J+
EB(5/04/15)
EB(5/08/15)
EB(5/11/15)
Aluminum
Calcium
Iron
Zinc
High
High
High
High
J+
J+
J+
J+
BG-1D(2) Aluminum RPD High J
MW-301BR(30-31) Barium RPD High J
MW-303BR(90-91.5) Calcium RPD High J
DUP-1 (collected
4/13/2015)
Aluminum
Iron
RPD High
RPD High
J
J
SB-3(1-2) Arsenic RPD High J
GWA-1D(30-31.5) Manganese RPD High J
VII. FIELD DUPLICATES
Field duplicate (FD) samples were collected. RPDs were not evaluated.
VIII. LABORATORY DUPLICATES
Laboratory duplicate (LD) analyses were performed on some samples from this project. Control
limits of 20% RPD, or less than the MRL for results less than five times the MRL, as suggested
in the Functional Guidelines, were met. No qualification was required.
IX. INSTRUMENT CALIBRATION
Instrument calibration requirements were met and no qualification was required except as noted
below.
Metals: Iron in one continuing calibration was recovered above control limits. Iron in the associated
sample MW-317BR(15-16) has been qualified as estimated with a possible high bias (J+).
X. SAMPLE REPORTING LIMITS
Most RLs were at or below the regulatory criteria (RSLs) for human health and the ecological
criteria (ESVs) except as noted in the table below. When an MDL is above the regulatory
criterion, results reported as non-detect cannot be assured to be below the criterion. In most
cases for these analytes, they were not reported as non-detect.
Analyte RL (mg/Kg) MDL (mg/Kg) RSL (mg/Kg) ESV (mg/Kg)
Antimony 3.7 1.9 ok 3.5
Arsenic 3.7 1.9 3.0 ok
Boron 18.7 9.4 ok 0.50
Chromium 1.9 0.94 ok 0.40
Thallium 3.7 1.9 1.2 1.0
Vanadium 3.7 1.9 ok 2.0
Duke Energy – Dan River Soil and Ash Page 7 of 7
XI. SAMPLE RESULTS / TRANSCRIPTION VERIFICATION
Transcription between the data package and the EDDs was verified. Results reported between
the MDLs and RLs were qualified as estimated (J).
TOC: The RSD for the quadruplicate analyses of TOC was above the control limit of 40% in
several samples, and these results have been qualified as estimated (J).
MW-306BR(40-41.5) [49.3%] MW-314BR(30-31.5) [86.6%]
MW-303BR(10-11.5) GWA-4D(28) [59%]
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l
m
g
/
l
m
g
/
l
m
g
/
l
m
g
/
l
u
g
/
l
m
g
/
l
D
T
D
T
D
T
D
T
N
N
N
T
N
0.
1
5
0
.
1
5
0
.
1
U
0
.
0
1
9
J
0
.
3
4
J
+
1
U
0
.
0
1
4
J
+
0
.
0
1
2
J
+
6
.
5
6
.
5
5
U
8
4
2
0
1
0
.
4
0.
7
4
0
.
7
9
0
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1
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0
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1
U
1
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1
.
3
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0
0
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0
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6
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1
8
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9
4
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8
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0
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4
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2
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1
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a
b
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1
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a
m
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l
e
s
-
F
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l
d
D
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i
c
a
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s
(
2
0
1
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1
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x
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Page 4 of 5
TA
B
L
E
E
-
1
QC
S
A
M
P
L
E
S
-
F
I
E
L
D
D
U
P
L
I
C
A
T
E
S
-
G
R
O
U
N
D
W
A
T
E
R
DA
N
R
I
V
E
R
S
T
E
A
M
S
T
A
T
I
O
N
DU
K
E
E
N
E
R
G
Y
C
A
R
O
L
I
N
A
S
,
L
L
C
,
E
D
E
N
,
N
C
Sa
m
p
l
e
N
a
m
e
S
a
m
p
l
e
I
D
P
a
r
e
n
t
I
D
AB
-
3
0
S
/
D
U
P
9
2
2
5
6
5
8
9
0
0
5
9
2
2
5
6
5
8
9
0
0
1
MW
-
3
0
6
B
R
D
U
P
2
0
1
5
0
1
9
7
4
6
2
0
1
5
0
1
9
7
4
5
Ge
n
e
r
a
l
N
o
t
e
s
:
ug
/
l
-
m
i
c
r
o
g
r
a
m
s
p
e
r
l
i
t
e
r
NA
-
N
o
t
a
n
a
l
y
z
e
d
o
r
n
o
t
r
e
p
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d
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-
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e
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o
t
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s
:
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-
-
N
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t
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t
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c
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t
.
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-
-
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-
E
s
t
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.
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Ma
g
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t
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2
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l
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s
NO
3
Po
t
a
s
s
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o
d
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To
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Ca
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To
t
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l
D
i
s
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o
l
v
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d
So
l
i
d
s
Total Suspended Solids
74
3
9
-
9
5
-
4
N
O
2
-
N
O
3
7
4
4
0
-
0
9
-
7
7
4
4
0
-
2
3
-
5
1
4
8
0
8
-
7
9
-
8
1
8
4
9
6
-
2
5
-
8
T
O
C
T
D
S
T
S
S
ug
/
l
m
g
/
l
u
g
/
l
u
g
/
l
m
g
/
l
m
g
/
l
m
g
/
l
m
g
/
l
m
g
/
l
T
N
T
T
N
N
N
N
N
53
0
0
0
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0
1
2
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0
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7
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4
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1
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0
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7
6
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1
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2
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29
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6
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x
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Page 5 of 5
TA
B
L
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E
-
1
QC
S
A
M
P
L
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-
F
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L
D
D
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L
I
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DA
N
R
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A
T
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DU
K
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G
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C
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S
,
L
L
C
,
E
D
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N
,
N
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e
N
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m
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t
I
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DU
P
-
1
2
0
1
5
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0
6
1
6
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5
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0
6
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0
DU
P
-
4
2
0
1
5
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1
5
5
2
4
2
0
1
5
0
1
5
5
0
4
DU
P
L
I
C
A
T
E
(
5
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9
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1
5
)
2
0
1
5
0
1
4
2
5
0
2
0
1
5
0
1
4
2
4
8
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p
l
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c
a
t
e
(
4
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2
8
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1
5
)
2
0
1
5
0
1
3
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2
0
1
5
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1
3
1
8
8
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p
l
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t
e
(
6
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7
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1
5
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0
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5
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8
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1
2
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5
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1
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1
9
Ge
n
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r
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s
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k
g
-
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l
l
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e
74
3
9
-
9
6
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5
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3
9
-
9
7
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6
7
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3
9
-
9
8
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4
0
-
0
2
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0
7
7
8
2
-
4
9
-
2
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2
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6
2
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6
6
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7
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0
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1
6
8
8
7
-
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-
6
7
4
3
9
-
9
5
-
4
1
4
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9
7
-
5
5
-
8
mg
/
k
g
m
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/
k
g
m
g
/
k
g
m
g
/
k
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m
g
/
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m
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g
m
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/
k
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k
g
m
g
/
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m
g
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g
T
T
T
T
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T
N
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N
32
.
5
J
+
0
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0
1
5
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-
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3
U
J
1
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8
3
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6
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2
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3
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3
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J
63
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x
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Page 2 of 3
TA
B
L
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-
1
QC
S
A
M
P
L
E
S
-
F
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D
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L
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P
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4
DU
P
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E
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5
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p
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Ge
n
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r
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s
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l
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)
.
x
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s
Page 4 of 18
TA
B
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-
2
QC
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A
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P
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S
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Q
U
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Page 5 of 18
TA
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Page 6 of 18
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Page 7 of 18
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Page 9 of 18
TA
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.
x
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Page 13 of 18
TA
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Page 14 of 18
TA
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Page 15 of 18
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Page 16 of 18
TA
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c:
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k
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\
t
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d
0
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(
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0
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)
.
x
l
s
Page 18 of 18