HomeMy WebLinkAboutNC0004774_CSA Report_20150823Comprehensive Site Assessment Report
Buck Steam Station Ash Basin
Site Name and Location
Groundwater Incident No.
NPDES Permit No.
Date of Report
Permittee and Current Property Owner
Consultant Information
Latitude and Longitude of Facility
Buck Steam Station
1555 Dukeville Road
Salisbury, NC 28146
Not Assigned
NC0004774
August 23, 2015
Duke Energy Carolinas, LLC
526 South Church St
Charlotte, NC 28202-1803
704.382.3853
HDR Engineering, Inc. of the Carolinas
440 South Church St, Suite 900
Charlotte, NC 28202
704.338.6700
350 71' 19" N, 800 37; 69" W
This document has been reviewed for accuracy and quality
commensurate with the intended application.
Thomas M. Yanoschak, P.E.
Senior Engineer
to DUKE
ENERGY
■aaneoar-
Malcolm Schaeffer, L.C.
Senior Geologist
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
EXECUTIVE SUMMARY
Executive Summary - Buck Steam Station
On August 20, 2014, the North Carolina General Assembly passed Session Law 2014-122, the
Coal Ash Management Act of 2014 (CAMA). N.C. Gen. Stat. § 130A-309.211 requires the
owner of a coal combustion residuals surface impoundment to submit a Groundwater
Assessment Plan (Work Plan) to the North Carolina Department of Environment and Natural
Resources (NCDENR) no later December 31, 2014 and a Groundwater Assessment Report
(herein referred to as a Comprehensive Site Assessment [CSA]) no later than 180 days
following approval of the Work Plan.
Duke Energy submitted a Work Plan to NCDENR on September 25, 2014 establishing proposed
site assessment activities and schedules for the implementation, completion, and submission of
a CSA report in accordance with 15A NCAC 02L .0106(g) for the Buck Steam Station (Buck).
NCDENR reviewed the Work Plan and provided Duke Energy with initial comments on
November 4, 2014. A revised Work Plan was subsequently submitted to NCDENR on
December 30, 2014 and NCDENR provided final comments and conditional approval of the
revised Work Plan on February 24, 2015. This CSA was prepared to comply with the CAMA and
is submitted to NCDENR within the allotted 180-day timeframe. Data generated during the CSA
will be used in development of the Corrective Action Plan (CAP), due 90 days after submittal of
this CSA. The purpose of this CSA is to characterize the extent of contamination resulting from
historical production and storage of coal ash, evaluate the chemical and physical characteristics
of the contaminants, investigate the geology and hydrogeology of the Site including factors
relating to contaminant transport, and examine risk to potential receptors and exposure
pathways. This CSA was prepared in general accordance with requirements outlined in the
following statutes, regulations and documents:
• Groundwater Classification and Standards, Title 15A North Carolina Administrative Code
(NCAC), Subchapter 2L
• Coal Ash Management Act of 2014, N.C. Gen. Stat. §§130A-309.200 et. seq.,
• Notice of Regulatory Requirements (NORR) issued by NCDENR on August 13, 2014,
• Conditional Approval of Revised Groundwater Assessment Work Plan issued by
NCDENR on February 24, 2015, and
• Subsequent meetings and correspondence between Duke Energy and NCDENR.
For this CSA, the source area is defined as the ash basin, which consists of the active ash basin
and the inactive ash basin. Source characterization was performed to identify physical and
chemical properties of ash, ash basin surface water, ash porewater, and ash basin seeps. The
ash, ash basin surface water, ash porewater, and seep analytical results were compared to 2L
Standards, IMACs, and other regulatory screening levels for the purpose of identifying
constituents of interest (COls). These COls are considered to be associated with potential
impacts to soil and groundwater from the ash basin.
This CSA also identifies constituents that exceeded 2L Standards or IMACs from groundwater
sample locations outside the ash basin boundary. For the purposes of this report, these
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constituents were also identified as COls. Some COls (e.g., iron and manganese) are present in
background and upgradient monitoring wells and thus require careful examination to determine
whether their presence downgradient of the ash basin is naturally occurring or a result of ash
handling and storage. Descriptions of COls outside the ash basin boundary are identified in
Section 10 (Groundwater Characterization) and Section 11 (Hydrogeological Investigation) of
this CSA. This inclusive approach to identification of COls will be refined during development of
the CAP to focus on those constituents that are attributable to the ash basin. COls were also
evaluated in the human health and ecological screening level risk assessment in Section 12.0.
In addition to evaluating the distribution of constituents across the Buck site, significant factors
affecting constituent transport, and the geological and hydrogeological features influencing the
movement and chemical and physical character of the COls were also evaluated.
Some Cols (e.g., antimony, cobalt, chromium, iron, manganese and vanadium) are also
present in background monitoring wells and thus require careful examination to determine
whether their presence downgradient of the ash basin or ash storage areas is naturally
occurring or a result of ash handling and storage.
The IMACs were issued in 2010, 2011 and 2012; however, NCDENR has not established a 2L
Standard for these constituents as described in 15A NCAC 2L.0202(c). For this reason, the
IMACs noted in this report are for reference only.
In addition to evaluating the distribution of constituents across the Buck site, significant factors
affecting constituent transport, the geological and hydrogeological features influencing the
movement and the chemical -physical character of the COls were also evaluated. The
assessment consisted of the following activities:
• Completion of soil and rock borings and installation of groundwater monitoring wells to
faciliatate collection and analysis of chemical, physical, and hydrogeological parameters
of subsurface materials encountered within and beyond the waste and compliance
boundaries.
• Evaluation of testing data to supplement the Site Conceptual Model (SCM).
• Revision to the Receptor Survey previously completed in 2014.
• Completion of a Screening -level Risk Assessment.
Based on scientific evaluation of historical and new data obtained during completion of the
above -referenced activities, the following conclusions can be drawn:
• No imminent hazard to human health or the environment has been identified as a result
of groundwater migration from the ash basin or ash storage areas.
• Recent groundwater assessment results are generally consistent with previous results
from historical and routine compliance boundary monitoring well data although some
new COls were identified due to a more robust sampling program.
• Upgradient, background monitoring wells contain naturally occurring metals and other
constituents at concentrations that exceeded their respective 2L Standards or IMACs.
This information is used to evaluate whether concentrations in groundwater
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downgradient of the basin and ash storage area are also naturally occurring, originate
from upgradient sources or might be influenced by migration of constituents from the ash
basin and ash storage area. Examples of naturally occuring metals and consituents
include antimony, chromium, cobalt, iron, manganese, and vanadium, which were all
detected in background groundwater samples at concentrations greater than 2L
Standards or IMACs.
Groundwater flow is predominately in the north direction toward the Yadkin River and is
downgradient from and not towards off -site receptors. However, there also is a
component of groundwater flow to the west of Cell 1 and there is localized flow in an
area east of the source that requires further evaluation (between Cells 2 and 3).
No information gathered as part of this CSA suggests that water supply wells or springs
within the 0.5-mile radius of the compliance boundary are impacted by the source, aside
from the single permitted well owned by Duke Energy.
The U.S. Environmental Protection Agency (USEPA) has identified constituents for
groundwater detection monitoring programs that can be used as indicators of
groundwater contamination from coal combustion residuals which may be evaluated for
statistically significant increases over background with time. Specifically, boron and
sulfate would be expected to migrate rapidly and would provide early detection as to
whether contaminants were migrating from the ash basin system. The horizontal and
vertical migration of boron best represents the groundwater flow and potential transport
system at the site. Sulfate, while generally a good indicator, can occasionally occur
naturally above its applicable standards and should be used as an indicator with more
caution. Sulfate exceedances at well locations outside the waste boundary appear to be
unrelated to the ash basin, and may be related to the bedrock geology. This is indicated
by the unique geochemistry and lack of boron observed at certain wells exhibiting
exceedances of sulfate, as well as the general lack of sulfate exceedances in ash basin
porewater. Figure ES-1 indicates the estimated horizontal extent of 2L Standard
exceedances for boron in the shallow, deep, and bedrock monitoring layers at the site.
The horizontal migration of boron in the flow layers best represent the dominant flow and
transport system in the vicinity of the ash basin and ash storage area. Vertical migration
of constituents is impeded but not eliminated by underlying bedrock. Boron is highly
soluble and was identified by the USEPA as one of the leading indicators for releases of
contaminants from ash. Because of these characteristics, boron can be used to
represent the general extent of the shallow, deep, and bedrock flow layers impacted by
the ash basin and ash storage area.
The approximate extent of groundwater impacted with COI exceedances attributable to
CCRs, such as boron, is limited to the shallow, deep, and bedrock flow layers beneath
the ash basin and ash storage area, and areas immediately downgradient of the ash
basin and ash storage area located to the north. Based on available data, it appears
groundwater impacted by the ash basin and ash storage area is contained within the
Duke Energy property boundary.
• There are no indications of boron exceedances of the 2L Standards or IMACs
upgradient from the Buck site.
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• The assessment identified potential soil and groundwater impacts. The approximate
extent of measured constituents is primarily limited to an area within the ash basin
compliance boundary and the area north of the compliance boundary to the Yadkin
River. There also appears to be a smaller component of groundwater flow west of ash
basin Cell 1 (and within the property boundary) resulting in potential movement of
constituents beyond the western compliance boundary between Cell 1 and the unnamed
tributary to the Yadkin River near the western extent of the Buck site.
• NCDENR identified seeps and CSA-identified seeps that contained water were sampled
during the CSA field program. The one NCDENR seep that could be sampled
(BSWW002 S001) did not exhibit USEPA ash indicator exceedances of the 2L
Standards.Samples obtained from CSA-identified seeps S-9 and TERRACOTTA PIPE
#1, both located near the base of the Cell 1 dam, were reported above the 2L Standard
for boron.
• Sediment was sampled at 14 active and dry seep locations. The only USEPA ash
related COI that exhibited an exceedance of the North Carolina Industrial Health and
Protection of Groundwater Preliminary Soil Remediation Goal (PSRG) was boron which
occurred at location TERRACOTTO PIPE #1.
• The data included in this CSA are to be used in the development of a Corrective Action
Plan, due 90 days after submittal of this CSA. This will include groundwater modeling to
evaluate the site's suitability to use monitored natural attenuation (MNA). If not
applicable, additional measures such as active remediation by hydraulic capture and
treatment, among others, would be evaluated. When properly applied, alternatives such
as these can provide effective long term management of sites requiring corrective action.
Brief summaries of essential portions of the CSA are presented in the following sections.
ESA Source Information
Duke Energy owns and formerly operated the Buck station, located on the Yadkin River in
Rowan County near the town of Salisbury, North Carolina. Buck began operation in 1926 as a
coal-fired generating station. The Buck Combined Cycle Station (BCCS) natural gas facility was
constructed at the site and began operating in late 2011. Subsequently, Buck was
decommissioned and taken offline in April 2013. The coal ash residue from Buck's coal
combustion process was historically disposed of in the station's ash basin system located
adjacent to the station and the Yadkin River. The discharge from the ash basin system is
permitted by the North Carolina Department of Environment and Natural Resources (NCDENR)
Division of Water Resources (DWR) under the National Pollutant Discharge Elimination System
(NPDES) Permit NC0004774.
Since 2006, Duke Energy has implemented voluntary and NPDES permit -required groundwater
monitoring at Buck. Twice per year voluntary groundwater monitoring around the Buck ash
basin was performed from November 2006 until May 2010, with analytical results submitted to
the NCDENR DWR. Compliance groundwater monitoring as required by the NPDES permit
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began in March 2011. From March 2011 through July 2015, the compliance groundwater
monitoring wells at Buck have been sampled three times per year for a total of 14 times.
The Buck ash basin system is located near the Yadkin River and comprises three cells
designated as Cell 1, Cell 2, and Cell 3, and associated embankments and outlet works. The
ash basin is located to the south (Cell 1) and southeast (Cells 2 and 3) of the retired Buck Units
through 6 and the BCCS. An area between Cell 1 and Cell 2 has also been utilized for storage
of dredged ash from Cell 1 and is referred to as the ash storage area. This unlined storage area
is located topographically upgradient and adjacent to the east side of Cell 1. The dry ash
storage area was constructed in 2009 by excavating ash within the eastern half of Cell 1 in
order to provide additional capacity for sluiced ash and covers approximately 14 acres.
All coal ash from Buck was disposed of in the ash basin from approximately 1957 until 2013. Fly
ash precipitated from flue gas and bottom ash collected in the bottom of the boilers were sluiced
to the ash basin using conveyance water withdrawn from the Yadkin River.
The ash basin system is operated as an integral part of the station's wastewater treatment
system, which receives permitted and variable discharges from the ash removal system, coal
pile runoff, landfill leachate, the station yard drain sump, and site stormwater.
ES.2 Initial Abatement and Emergency Response
No imminent hazard to human health or the environment has been identified; therefore, initial
abatement and emergency response actions are not required.
ES.3 Receptor Information
Properties located within a 0.5-mile radius of the Buck ash basin compliance boundary generally
consist of residential, agricultural, and undeveloped properties located in Rowan County to the
west, south, and east of the ash basin. The Yadkin River flows east along the northern
boundary. Hunting and game lands are located north of the ash basin system across the Yadkin
River in Davidson County.
Duke Energy submitted a receptor survey to NCDENR (HDR 2014a) in September 2014, and
subsequently submitted to NCDENR a supplement to the receptor survey (HDR 2014b) in
November 2014 based on the CSA Guidelines. The update included contacting and/or
reviewing the agencies/records to identify public and private water supply sources identified and
reviewing questionnaires that were received after the submittal of the November 2014
supplement to the September 2014 receptor survey (i.e. questionnaires received after October
31, 2014).
The purpose of the receptor survey was to identify the exposure locations that are critical to be
considered in the groundwater transport modeling and human health risk assessment.
The CSA receptor survey activities included contacting and/or reviewing the following
agencies/records to identify public and private water supply sources, confirm the location of
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wells, and/or identify any wellhead protection areas located within a 0.5-mile radius of the Buck
ash basin compliance boundary:
• NCDENR Division of Water Resources (DWR) Public Water Supply Section's (PWSS)
most current Public Water Supply Water Sources GIS point data set;
• NCDENR DWR Source Water Assessment Program (SWAP) online database for public
water supply sources;
• Environmental Data Resources (EDR) local/regional water agency records review;
• Rowan County Health Department Environmental Health Division;
• Davidson County Health Department;
• Salisbury -Rowan Utilities Department; and
• USGS National Hydrography Dataset.
The review of these records identified a total of 166 private water supply wells within a 0.5-mile
radius of the Buck ash basin compliance boundary. The Rowan County Health Department had
records for 28 of the 166 identified private water supply wells. Ten additional private water
supply wells are assumed to exist since well houses could not be visually observed at these
residences located within a 0.5-mile radius of the Buck ash basin compliance boundary. Two
public water supply wells were identified within a 0.5-mile radius of the Buck ash basin
compliance boundary. One water supply well was identified within the Duke Energy property
boundary that supplies drinking water to the site.. Several unnamed tributaries of the Yadkin
River were identified within a 0.5-mile radius of the ash basin, and several surface water
features that flow toward the Yadkin River were identified within a 0.5-mile radius of the Buck
ash basin.
ESA Sampling / Investigation Results
ES.4.1 Background Findings
As part of the CSA, Duke Energy installed seven additional nested wells (three shallow, two
deep, one upper bedrock, and one bedrock monitoring well) in selected areas of the site
upgradient from the ash basin and ash storage area to supplement the existing nested shallow
and deep monitoring wells (installed in 2006) by providing additional background soil and
groundwater quality data. The COI concentration range in background groundwater samples
which exceeded the 2L Standard are provided below.
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
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EXECUTIVE SUMMARY
Constituent of Interest
Groundwater 2L Standard
or IMACs (Ng/L)
Range of Exceedances
Antimony
1
3.8 pg/L to 5.8 Ng/L
Chromium
10
0.22J pg/L to 10.3 pg/L
Cobalt
1
4 Ng/L to 7.2 pg/L
Iron
300
306J Ng/L to 1,900 pg/L
Manganese
50
54 pg/L to 850 Ng/L
Vanadium
0.3
0.86J pg/L to 26.6 pg/L
These COls were found to be present within groundwater monitoring wells at several locations
across the site. Their presence within the background wells at concentrations exceeding the 2L
or IMAC Standards requires analysis to determine whether downgradient exceedances are due
to natural condition or impacts from the ash basin and ash storage area.
ES.4.2 Nature and Extent of Contamination
Soil and groundwater beneath the ash basin and ash storage area has been impacted by ash
handling and storage at the Buck site. Concentrations of several COls appear to exceed their
respective 2L Standards or IMACs in groundwater beyond the compliance boundary toward the
Yadkin River, although some of these COls also exceed 2L in the background wells. These
exceedances appear contained on Duke Energy Property. Samples obtained from on -site
seeps also exhibit concentrations of COls exceeding their respective 2L Standards or IMACs.
ES.4.2.1 Groundwater - Shallow Flow Layer
Within the shallow flow layer (including beneath the ash storage area), there are five Cols
identified as in the groundwater in multiple groundwater samples: cobalt, chromium, iron,
manganese, and vanadium. All of these COls also appear within one or more of the background
well locations at concentrations exceeding the applicable groundwater standard. Almost all of
the iron exceedances within the shallow aquifer (12 of 13) occurred within unfiltered samples
indicating the source of the iron within the shallow groundwater samples is primarily suspended
solids. Six other COls identified in the shallow flow layer are antimony, boron, nickel, selenium,
sulfate, and Total Dissolved Solids, but they are in isolated locations.
ES.4.2.2 Groundwater - Deep Flow Layer
Within the deep flow layer (including beneath the ash basin and ash storage area), there are
seven COls identified in the groundwater (D wells): antimony, boron, chromium, cobalt, iron,
manganese, and vanadium. Vanadium also appears within three of the deep flow layer
background well locations at concentrations exceeding the applicable 2L Standard or IMAC.
Almost all of the iron exceedances within the deep flow layer (10 of 12) occurred within
unfiltered samples indicating the source of the iron within the deep flow layer groundwater
samples is primarily suspended solids. Two other COls identified in the deep flow layer are
sulfate and TDS, but they are in isolated locations.
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ES.4.2.3 Groundwater — Bedrock Flow Layer
Within the bedrock flow layer (including beneath the ash basin), there are four COls identified in
the groundwater (BR and BRU wells): antimony, chromium, iron, manganese, and vanadium.
None of these COls appear within the bedrock background well location (BG-3BRU) at a
concentration exceeding the applicable groundwater standard. All eight of the iron exceedances
within the bedrock flow layer occurred within unfiltered samples indicating the source of the iron
within the bedrock groundwater samples is primarily suspended solids. Six other COls identified
in the bedrock flow layer are barium, boron, cobalt, selenium, sulfate and TDS, but they are in
isolated locations.
ES.4.2.4 Seep Samples
Seep sampling results at the Buck site have identified nine Cols in the seep water: antimony,
arsenic, boron, chromium, cobalt, iron, manganese, thallium, and vanadium. Comparing COI
concentrations in the seep water to the maximum COI concentrations encountered in
groundwater sampled from the background wells indicates nine seep locations (BSWW002
S001, Terracotta Pipe #1, Culvert Discharge, S-1, S-2, S-3, S-5, S-8, and S-9) where at least
one seep COI concentration exceeded the maximum background groundwater COI
concentration (arsenic, boron, chromium, cobalt, iron, manganese, thallium, and vanadium) .
ES.4.2.5 Soil, Rock and Sediment Concentrations
Soil samples were obtained from 29 separate locations during CSA drilling activities within the
Buck site (including locations beneath the ash basin and ash storage area). Eight Cols were
identified in soil samples obtained from these locations: arsenic (5 locations), barium (1
location), boron (4 locations), cobalt (29 locations), iron (29 locations), manganese (29
locations), selenium (5 locations), and vanadium (29 locations). With the exception of barium, all
of these COls appear in one or more of the background well locations at concentrations
exceeding the most restrictive PSRG standard. The COI concentrations observed in the soil
from the various locations within the Buck site generally bracket the concentrations observed in
soil samples from the background locations or within reasonable proximity of the bracketed
background concentrations.
Rock samples (including partially weathered rock [PWR] samples) were obtained from ten
separate locations during CSA drilling activities within the Buck site, including locations beneath
the ash basin and ash storage area. Five COls were identified in rock samples obtained from
these locations: arsenic (1 location), cobalt (8 locations), iron (10 locations), manganese (9
locations), and vanadium (8 locations). With the exception of arsenic, all of these COls appear
within the background location where rock was obtained (BG-2) at concentrations exceeding the
most restrictive PSRG standard.
Sediment samples were obtained from 14 seep locations at the Buck site. Seven COls were
identified in the sediment samples: arsenic (4 locations), boron (1 location), cobalt (all
locations), iron (all locations), manganese (13 locations), selenium (1 location) and vanadium
(all locations). A background sediment location (SW-2) was not obtained due to dry conditions
at the time of sampling; therefore a comparison of these results with background conditions is
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not possible at this time. Such a comparison may be possible after completion of the second
comprehensive sampling event and will be included in the CSA supplement.
ES.4.3 Maximum Contaminant Concentrations
The maximum contaminant concentrations reported in groundwater, ash porewater, seep water,
and ash basin surface water samples collected during the CSA are listed below.
Maximum Constituent of Interest (COI) Concentrations
COI
Background
wells
Groundwater
(Ng/L)
Ash Porewater
(N9/L)
Seep Water
(N9/L)
Ash Basin Surface
Water
(Ng/L)
Aluminum
160
n/a
n/a
n/a
13,000
Antimony
5.8
19.3
24.4
1.8
n/a
Arsenic
11
14.9
1,350
38.6
71.3
Barium
86
830
720
n/a
n/a
Boron
49J
3,000
6,500
820
n/a
Cadmium
0.025J
n/a
n/a
n/a
0.37
Chromium
10.3
65.4
n/a
32.7
n/a
Cobalt
6.8
356
44.7
41.1
23.9
Copper
45.8
n/a
n/a
n/a
32.4
Iron
1,900
27,900
44,700
34,900
n/a
Lead
0.24
n/a
n/a
n/a
12.7
Manganese
850
4,100
3,900
3,900
n/a
Nickel
10.9
107
n/a
n/a
n/a
Selenium
0.39J
30.3
n/a
n/a
n/a
Sulfate
22,700
703,000
n/a
n/a
n/a
TDS
175,000
1,046,000
565,000
n/a
n/a
Thallium
0.032J
0.24
0.67
n/a
0.45
Vanadium
26.6
67.9
347
132
n/a
Zinc
77
n/a
n/a
n/a
50
J = Estimated Concentration
ES.4.4 Source Characterization
Source characterization was performed through the completion of borings and installation of
groundwater monitoring wells within the footprint of the ash basin cells, ash storage area,
associated solid matrix (ash), and aqueous sample (ash porewater),and the collection and
analysis of samples. Ash samples were collected for analysis of physical characteristics (e.g.,
grain size, porosity, etc.) to provide data for evaluation of retention/transport properties within
and beneath the ash basin and ash storage area. Ash samples were collected for analysis of
chemical characteristics (e.g., total inorganics, leaching potential, etc.). The results of the
characterization will be used to refine the CSM and to provide data for use in the CAP.
Review of laboratory analytical results of ash samples collected from the ash basin and ash
storage area identified eight COls including arsenic, cobalt, barium, boron, cobalt, iron,
manganese, selenium, and vanadium. COls identified in ash basin porewater include antimony,
arsenic, barium, boron, cobalt, iron, manganese, thallium, and vanadium. COls identified in ash
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basin surface water include aluminum, antimony, arsenic, cadmium, cobalt, copper, lead,
thallium, and zinc.
SPLP (Synthetic Precipitation Leaching Procedure) testing was conducted to evaluate the
leaching potential of Cols from ash. Although SPLP analytical results are being compared to
the 2L Standards and IMACs, these samples do not represent groundwater samples. The
results of SPLP analyses indicated that the following COls exceeded their 2L Standards:
antimony, arsenic, chromium, cobalt, iron, manganese, selenium, thallium, and vanadium.
However, many factors influence the transport of these COls and any potential impacts to
groundwater over time will be investigated through modeling as part of the CAP.
There are 14 seeps (S-1 through S-10, Culvert Discharge, Wet Area Near Pump House,
Terracotta Pipe #1, and Terracotta Pipe #2) located within the Duke Energy property boundary
and three seeps (S-1 A, S-1 B, and S-1 C) located outside of the Duke Energy property boundary
associated with the ash basin at the Buck site, excluding the "NCDENR seeps." Duke Energy
was not able to obtain permission from the property owner to obtain off -site seep samples S-1A,
S-1 B, and S-1 C; therefore these seeps were not sampled. Twelve of the 14 on -site seeps were
sampled as the remaining seeps (Wet Area Near Pump House and Terracotta Pipe #2) were
dry on the day of sampling. Of the seep locations sampled in time for this report, seven COls
were reported exceeding the 2L Standards: boron, chromium, cobalt, iron, manganese, thallium,
and vanadium.
There are six NCDENR seep locations identified at Buck for sampling. Only one seep,
BSWWO02 S001, was active on the day of sampling and the rest were dry. Samples collected
from BSWWO02 S001 exceeded the 2L or IMAC Standards for the following COls: antimony,
arsenic, iron, manganese, and vanadium.
ES.4.5 Regional Geology and Hydrogeology
The Buck site is within the Charlotte terrane, one of a number of tectonostratigraphic terranes
that have been defined in the southern and central Appalachians and is in the western portion of
the larger Carolina superterrane (Horton et al. 1989; Hibbard et al. 2002; Hatcher et al. 2007).
On the northwest side, the Charlotte terrane is in contact with the Inner Piedmont zone along
the Central Piedmont suture along its northwest boundary and is distinguished from the Carolina
terrane to the southeast by its higher metamorphic grade and portions of the boundary may be
tectonic in origin (Secor et al. 1998; Dennis et al. 2000).
The Charlotte terrane is dominated by a complex sequence of plutonic rocks that intrude a suite
of meta -igneous rocks (amphibolite metamorphic grade) including mafic gneisses, amphibolites,
meta-gabbros, and metavolcanic rocks with lesser amounts of granitic gneiss and ultramafic
rocks with minor metasedimentary rocks including phyllite, mica schist, biotite gneiss, with
quartzite and marble along its western portion (Butler and Secor 1991; Hibbard et al. 2002). The
general structure of the belt is primarily a function of plutonic contacts.
The groundwater system in the Piedmont region is described as being comprised of two
interconnected layers, or two -medium system: 1) residual soil/saprolite and weathered fractured
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rock (regolith) overlying 2) fractured crystalline bedrock. The regolith layer is a thoroughly
weathered and structureless residual soil that occurs near the ground surface with the degree of
weathering decreasing with depth. The residual soil grades into saprolite, a coarser grained
material that retains the structure of the parent bedrock. Beneath the saprolite, partially
weathered/fractured bedrock occurs with depth until sound bedrock is encountered. This mantle
of residual soil, saprolite, and weathered/fractured rock is a hydrogeologic unit that covers and
crosses various types of rock (LeGrand 1988). This regolith layer serves as the uppermost zone
of the unconfined groundwater system and provides an intergranular medium through which the
recharge and discharge of water to and from the underlying fractured rock occurs. A transition
zone (TZ) of higher hydraulic conductivity at the base of the regolith is present in many areas of
the Piedmont (Schaeffer 2014a).
Typically, the residual soil/saprolite is partially saturated and the water table fluctuates within it.
Water movement is generally preferential through the overlying soil and saprolite and
weathered/fractured bedrock of the TZ. The character of such layers results from the combined
effects of the rock type, fracture system, topography, and weathering. Topography exerts an
influence on both weathering and the opening of fractures, while the weathering of the
crystalline rock modifies both transmissive and storage characteristics.
ES.4.6 Site Geology and Hydrogeology
The Buck site and its associated ash basin and ash storage areas are located in the Charlotte
terrane. The Charlotte terrane consists of an igneous complex of Neoproterozoic to Paleozoic
ages (Hibbard et al, 2002) that range from felsic to mafic in composition (Butler and Secor
1999). The Charlotte terrane is bordered on the east and southeast by the Carolina terrane and
to the west and northwest by the Inner Piedmont (Cat Square and Tugaloo terranes) and the
Kings Mountain terrane. The structural contact of the Inner Piedmont and Charlotte terrane is
the Central Piedmont Shear Zone.
The Buck site is underlain by interbedded felsic, intermediate, and mafic metavolcanic rocks.
The felsic metavolcanic rocks are fine- to medium -grained, locally coarse -grained or
agglomeritic, rhyolitic to dacitic metatuffs. The intermediate and mafic metavolcanic rocks are
fine- to medium -grained, locally coarse -grained or agglomeritic rocks of basaltic, andesitic, and
dacitic compositions. They are primarily tuffs and flows and with minor hypabyssal intrusives
present. The rocks are metamorphosed to the upper amphibolite grade of metamorphism.
Based on the site investigation, the groundwater system in the natural materials (alluvium, soil,
soil/saprolite, and bedrock) at Buck is consistent with the Piedmont regolith-fractured rock
system and is an unconfined, connected system of three flow layers. In general, groundwater
within the shallow, deep (TZ), and bedrock layers flows radially from the ash basins and
nouthward toward the Yadkin River.
ES.4.7 Existing Groundwater Monitoring Data
Twelve monitoring wells were installed by Duke Energy in 2006 as part of a voluntary
groundwater monitoring system near the ash basin. Voluntary monitoring wells MW-2S and
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MW-2D were abandoned during construction of the Buck Combined Cycle Station. With the
exception of MW-6S, MW-6D, MW-3S, and MW-3D, no samples are currently being collected
from the voluntary wells, and as a result, they are not included in this CSA.
Compliance groundwater monitoring as required by the Buck NPDES Permit NC0004774 began
in March 2011 and includes 14 wells. NPDES Permit Condition A (11), Version 1.1, dated June
15, 2011, lists the groundwater monitoring wells to be sampled, the parameters and constituents
to be measured and analyzed, and the requirements for sampling frequency and reporting
results (provided in Table 2-1). Locations for the compliance groundwater monitoring wells were
approved by the NCDENR DWR or it predecessor.
One or more groundwater quality standards (2L Standards) have been exceeded in
groundwater samples collected from each of the compliance monitoring wells. Exceedances
have occurred for boron, chromium, iron, manganese, pH, sulfate, and total dissolved solids
(TDS).
ES.4.8 Screening -Level Risk Assessment
The prescribed goal of the human health and ecological screening level risk assessments is to
evaluate the analytical results from the COI sampling and analysis effort and using the various
criteria taken from applicable guidance, determine which of the COls may present an
unacceptable risk, in what media, and therefore, should be carried through for further evaluation
in a baseline human health or ecological risk assessment or other analysis, if required.
Constituents of Probable Concern (COPCs) are those COls that have been identified as having
possible adverse effects on human or ecological receptors that may have exposure to the
COPCs at or near the site. The COPCs serve as the foundation for further evaluation of
potential risks to human and ecological receptors.
To support the CSA effort and inform corrective action decisions, a screening level evaluation of
potential risks to human health and the environment to identify preliminary, media -specific
COPCs has been performed in accordance with applicable federal and state guidance, including
the Guidelines for Performing Screening Level Ecological Risk Assessments within the North
Carolina Division of Waste Management (NCDENR, 2003). The criteria for identifying COPCs
vary by the type of receptor (human or ecological) and media, as shown in the comparison of
contaminant concentrations in various media to corresponding risk -based screening levels
presented in Tables 12-1 through 12-9.
COls were not screened out as COPCs based on a comparison to background concentrations,
as the NCDENR Division of Waste Management's Screening Level Environmental Risk
Assessment guidance (2003) does not allow for screening based on background. Site -specific
background concentrations will be considered in the uncertainty section of the baseline
ecological risk assessment, if determined to be necessary.
This initial screening, does not specifically identify that health or environmental risks are
present, rather the results indicate constituents in the environmental media for further
investigation by a site -specific risk assessment. It should be noted that the observed levels of
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certain COls in the naturally occurring background at Buck would also warrant consideration of
a BERA. N
ES.4.9 Development of Conceptual Site Model
The human health and ecological risk assessment conceptual site models, illustrating potential
pathways of exposure from source to receptors are provided in this report.
In the initial site conceptual hydrogeologic model presented in the Work Plan, the geological and
hydrogeological features influencing the movement, chemical, and physical characteristics of
contaminants were related to the Piedmont hydrogeologic system at the site.
A hydrogeological site conceptual model was developed from data generated during previous
assessments, existing groundwater monitoring data, and 2015 groundwater assessment
activities. Groundwater flow is predominately in the north direction toward the Yadkin River and
is downgradient from and not towards off -site receptors. However, there also is a component of
groundwater flow to the west of Cell 1 and there is localized flow in an area east of the source
that requires further evaluation (between Cells 2 and 3).
ES.4.10 Identification of Data Gaps
Through completion of groundwater assessment field activities and evaluation of data collected
during those activities, Duke Energy has identified data gaps that will require further evaluation
to refine the CSM. The data gaps have been separated into three groups: 1) data gaps resulting
from temporal constraints, 2) data gaps resulting from evaluation of data collected during the
CSA, and 3) data gaps resulting from other sources.
ES.4.10.1 Data Gaps Resulting from Temporal Constraints
Data gaps identified in this category are generally present due to insufficient time to collect,
analyze, or evaluate data collected during the CSA activities. It is expected that the majority of
these data gaps will be remedied in a CSA supplement to be submitted to NCDENR following
completion of the second comprehensive groundwater sampling event.
• Mineralogical Characterization of Soil and Rock — a total of 16 soil, three TZ, and 9
bedrock samples were submitted to three third -party mineralogical testing laboratories
for analysis of soil and rock composition. As of the date of this report, Duke Energy has
not received all of the results of this testing; however, results will be provided in the CSA
supplement.
• Additional Speciation of Monitoring Wells — In order to meet the requirements of the
NORR, Duke Energy conducted speciation of groundwater samples for arsenic,
chromium, iron, manganese, and selenium from selected wells along inferred
groundwater flow transects. Adjustments to the speciation sampling are proposed in
Section 15.0, the results of which will be reported in the CSA supplement.
• Dry Sampling Locations — Due to dry conditions at the time of the initial sampling event,
several proposed surface water and seep sampling locations were dry and could not be
sampled. Another attempt to sample these locations will be made during the second
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comprehensive groundwater sampling event. If successful, the results will be provided in
the CSA supplement. These locations include:
o Surface water locations SW-1 and SW-2 located along an unnamed tributary to the
Yadkin River on the east side of the Buck site.
o On -site seeps:. Seeps identified as Wet Area Near Pump House and Terracotta
Pipe #2 were dry and could not be sampled.
o NCDENR seep locations BS SWO01 AA S001, BS SWO03AA S001, BSSWO01 S001,
BSSW074SO01, and BSSW074SO01.
ES.4.10.2 Data Gaps Resulting from Review of Data Obtained During CSA Activities
• A shallow groundwater monitoring well in the nest of GWA-2BRU and GWA-2BR would
assist with the groundwater flow direction determination in this location. Additional
monitoring well nests nortwest and southwest of GWA-2BRU/BR would assist in refining
groundwater flow direction in this area and provide information regarding constituent
concentrations between the Cell 2 Primary Pond and the southern pond associated with
the Cell 3 Secondary Pond.
• The bedrock background monitoring well BG-1 BR could not be sampled due to
insufficient water in the well during the sampling event. A replacement bedrock
background well in this location may be warranted if BG-1 BR is not a viable well. Also, a
bedrock well installed at the BG-3S/D would provide additional data regarding
background bedrock concentrations at the site.
• Groundwater samples were not collected from all of the onsite voluntary wells or existing
monitoring wells that were installed during the site closure investigation. During
subsequent sampling events, groundwater elevations will be measured and groundwater
samples will be collected from these wells in conjunction with the newly installed
assessment monitoring wells.
• The vanadium method reporting limit provided by the analytical laboratory was 1.0 ug/L.
The IMAC for vandium is 0.3 ug/L. The vanadium results reported at concentrations less
than the laboratory method reporting limit are estimated. During subsequent monitoring
events, a laboratory method reporting equal to or less than the IMAC should be utilized.
• Review of Non -Ash Contamination Information: Review of information regarding areas of
non -ash contamination (i.e., petroleum -contaminated areas) to evaluate potential
interference with remedial methods is needed, if applicable.
• Obtain soil samples located outside of the ash basin for SPLP analysis to compare
results against SPLP analysis of ash.
• Perform mineralogy analysis of soil and rock samples in wells where COls are present
above 2L or IMAC Standards to determine if constituents occur naturally
ES.4.10.3 Data Gaps Resulting from Other Sources
• Sampling of Off -Site Seeps — the Work Plan included obtaining a surface water sample
(S-1A) and samples at two seep locations (S-1 B and S-1 C) associated with an off -site
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pond located near the eastern extent of Duke Energy's property boundary. Duke Energy
was not able to obtain permission from the property owner to collect these samples.
ES.5 Conclusions
The CSA found that the source and cause of impacts (as shown on figure ES-1) for certain
parameters in some areas of the site is the coal ash contained in the ash basin and ash storage
area. The cause of this contamination, shown on the referenced figure, is leaching of
constituents from the coal ash into the underlying soil and groundwater and subsequent
transport of the groundwater downgradient from the ash basin. However, some groundwater,
surface water and soil standards were also exceeded due to naturally occurring elements found
in the subsurface.
The CSA found no imminent hazards to public health and safety; therefore, no actions to
mitigate imminent hazards are required. However, corrective actions at the Buck site are
required to address soil and groundwater contamination shown on Figure ES-1. These will be
addressed as part of the CAP.
The CSA identified the horizontal and vertical extent of groundwater contamination within the
compliance boundary (as shown in figure ES-1), and found that the source and cause of the
groundwater exceedances within that boundary is a result of both natural conditions and the
coal ash contained in the ash basin and ash storage area. In general, COls exceeding 2L
Standards or IMACs on the northern side of the waste boundary are judged to be highly
influenced by the source. Some of these exceedances were measured outside the compliance
boundary, although within the Duke Energy property boundary.
Background monitoring wells contain naturally occurring metals and other constituents at
concentrations that exceeded their respective 2L Standards or IMACs. Examples of naturally
occurring constituents include antimony, cobalt, iron, manganese, and vanadium. Some of these
naturally occurring constituents were also detected in newly installed background monitoring
well groundwater samples at concentrations greater than 2L Standards or IMACs.
The horizontal and vertical extent of groundwater impacts above 2L Standards or IMACs is
shown, with exception of the areas associated with the data gaps identified in Section 14.1 on
Figures 10-10 through 10-51. Groundwater contamination is considered to be present where the
analytical results were greater than the site background concentrations and in excess of the 2L
Standards or IMACs. The assessment found COI groundwater concentrations above
background concentrations for antimony, arsenic, barium, boron, chromium, cobalt, iron,
manganese, nickel, selenium, thallium, vanadium, sulfate, and TDS. The approximate extent of
groundwater contamination is shown on these figures and is generally limited to an area within
the ash basin compliance boundary and the area north of the compliance boundary near the
Yadkin River (within the Duke Energy property boundary). Exceedances measured south, east,
and west of the waste boundary are judged to be predominately related to natural conditions,
although some source related exceedances were identified. All source related exceedances are
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judged to be within the compliance boundary in these areas; however, some data gaps were
identified as discussed in Section 17.
The CSA found that the primary direction of flow and mobile contaminant transport is
predominately to the north toward the Yadkin River (within the Duke Energy property
boundaries) and not towards other off -site receptors. No information gathered as part of this
CSA suggests that water supply wells or springs within the 0.5-mile radius of the compliance
boundary are impacted by the source.
This CSA also identified the horizontal and vertical extent of soil contamination as shown on
Figures 8-1 through 8-4. Soil contamination is considered to be present where analytical results
for COls were in excess of the maximum site soil background concentrations and in excess of
the most restrictive PSRG for each COI. The approximate contaminated soil extent is shown on
these figures. The assessment found the soil contaminants in excess of the maximum
background soil COI concentrations are arsenic, barium, boron, and iron.
Groundwater flow is predominately in the north direction toward the Yadkin River. However,
there also is a component of groundwater flow to the west of Cell 1 and there is localized flow in
an area east of the source that requires further evaluation (between Cells 2 and 3).
Exceedances of COls have been observed in monitoring wells in these areas and near the ash
basin west compliance boundary. The exceedances, however, do not include COls identified by
the USEPA as indicators of CCR related contamination. Further, the constituents identified with
exceedances to the south, east and west of the source have also been identified in the
background wells.
In accordance with CAMA, Duke Energy is required to implement closure and remediation of the
Buck ash basin no later than August 1, 2029. Closure for the Buck ash basin was not defined in
CAMA. However, CAMA does require Duke Energy to submit a proposed CAP such that
NCDENR can prioritize site closure based on risk classifications.
No later than December 31, 2015, NCDENR is to develop proposed classifications for all coal
combustion residuals surface impoundments, including active and retired sites, for the purpose
of closure and remediation. At which time a schedule for closure and required remediation that
is based on the degree of risk to public health, safety and welfare, the environment, and natural
resources posed by the impoundments and that gives priority to the closure and required
remediation of impoundments that pose the greatest risk (CAMA 2014).
The classification for the Buck ash basin will be based upon this CSA and the corrective action
plan (CAP) which is to be submitted within 90 days of submittal of the CSA. The risk
classifications as described in CAMA include:
(1) High -risk impoundments shall be closed as soon as practicable, but no later than
December 31, 2019. A proposed closure plan for such impoundments must be submitted
as soon as practicable, but no later than December 31, 2016.
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(2) Intermediate -risk impoundments shall be closed as soon as practicable, but no later
than December 31, 2024. A proposed closure plan for such impoundments must be
submitted as soon as practicable, but no later than December 31, 2017.
(3) Low -risk impoundments shall be closed as soon as practicable, but no later than
December 31, 2029. A proposed closure plan for such impoundments must be submitted
as soon as practicable, but no later than December 31, 2018.
Following NCDENR's risk classification determination, a Closure Plan for the ash basin is to be
submitted for NCDENR's approval (CAMA 2014).
Based on the findings of this CSA report, the future CAP, NCDENR's risk classification, and the
approved Closure Plan, appropriate action will be taken for ash basin closure.
In the subsequent CAP, Duke Energy will pursue corrective action under 15A NCAC 02L .0106
(k) or (1) depending on the results of the groundwater modeling and the evaluation of the site's
suitability to use MNA. This would potentially require evaluation of MNA using the approach
found in Monitored Natural Attenuation of Inorganic Contaminants in Groundwater, Volumes 1
and 2 (EPA Reference) and the potential modeling of groundwater surface water interaction. If
these approaches are found to not be satisfactory, additional measures such as active
remediation by hydraulic capture and treatment, among others, would be evaluated. When
properly applied, alternatives such as these can provide effective long term management of
sites requiring corrective action.
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TABLE OF CONTENTS
Table of Contents
Section Page No.
1.0
Introduction........................................................................................................................1
1.1
Purpose of Comprehensive Site Assessment................................................................1
1.2
Regulatory Background..................................................................................................2
1.2.1 NCDENR Requirements..........................................................................................2
1.2.2 Notice of Regulatory Requirements........................................................................3
1.2.3 Coal Ash Management Act Requirements..............................................................3
1.3
NCDENR-Duke Energy Correspondence.......................................................................4
1.4
Approach to Comprehensive Site Assessment..............................................................4
1.4.1 NORR Guidance.....................................................................................................5
1.4.2 USEPA Monitored Natural Attenuation Approach...................................................5
1.4.3 ASTM Conceptual Site Model Guidance.................................................................5
1.5
Limitations and Assumptions..........................................................................................6
2.0
Site History and Description...............................................................................................8
2.1
Site Location, Acreage, and Ownership.........................................................................8
2.2
Site Description..............................................................................................................8
2.3
Adjacent Property, Zoning, and Surrounding Land Uses...............................................9
2.4
Adjacent Surface Water Bodies and Classifications.......................................................9
2.5
Meteorological Setting..................................................................................................10
2.6
Hydrologic Setting........................................................................................................10
2.7
Permitted Activities and Permitted Waste....................................................................11
2.8
NPDES and Surface Water Monitoring........................................................................12
2.9
NPDES Flow Diagram..................................................................................................12
2.10
History of Site Groundwater Monitoring........................................................................12
2.10.1 Voluntary Groundwater Monitoring Wells..............................................................13
2.10.2 Compliance Groundwater Monitoring Wells..........................................................13
2.11
Assessment Activities or Previous Site Investigations..................................................14
2.12
Decommissioning Status..............................................................................................14
3.0
Source Characteristics.....................................................................................................16
3.1
Coal Combustion and Ash Handling System................................................................16
3.2
Description of Ash Basins and Ash Storage Area........................................................16
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3.2.1 Ash Basin..............................................................................................................17
3.2.2 Ash Storage Area..................................................................................................18
3.2.3 Dams.....................................................................................................................18
3.3 Physical Properties of Ash............................................................................................19
3.4 Chemical Properties of Ash..........................................................................................19
4.0 Receptor Information........................................................................................................22
4.1 Summary of Previous Receptor Survey Activities........................................................22
4.2 Summary of CSA Receptor Survey Activities and Findings.........................................23
4.3 NCDENR Well Water Testing Program........................................................................25
5.0 Regional Geology and Hydrogeology..............................................................................26
5.1 Regional Geology.........................................................................................................26
5.2 Regional Hydrogeology................................................................................................26
6.0 Site Geology and Hydrogeology......................................................................................29
6.1 Site Geology.................................................................................................................29
6.1.1 Soil Classification..................................................................................................29
6.1.2 Rock Lithology.......................................................................................................30
6.1.3 Structural Geology.................................................................................................30
6.1.4 Geologic Mapping.................................................................................................30
6.1.5 Fracture Trace Study.............................................................................................31
6.1.6 Effects of Geologic Structure on Groundwater Flow.............................................32
6.1.7 Soil and Rock Mineralogy and Chemistry.............................................................32
6.2 Site Hydrogeology........................................................................................................33
6.2.1 Groundwater Flow Direction..................................................................................33
6.2.2 Hydraulic Gradient.................................................................................................33
6.2.3 Effects of Geologic/Hydrogeologic Characteristics on Contaminants ...................34
6.2.4 Site Hydrogeologic Conceptual Model..................................................................34
7.0 Source Characterization...................................................................................................36
7.1 Ash Basin.....................................................................................................................37
7.1.1 Ash (Sampling and Chemical Characteristics)......................................................37
7.1.2 Ash Basin Surface Water (Sampling and Chemical Characteristics) ....................38
7.1.3 Ash Porewater (Sampling and Chemical Characteristics).....................................38
7.1.4 Ash Porewater Speciation.....................................................................................
39
7.1.5 Radiological Laboratory Testing............................................................................39
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7.2 Ash Storage Area.........................................................................................................39
7.2.1 Ash (Sampling and Chemical Characteristics)......................................................39
7.2.2 Ash Porewater (Sampling and Chemical Characteristics).....................................40
7.3 Seeps...........................................................................................................................40
7.3.1 Review of NCDENR March 2014 Sampling Results.............................................40
7.3.2 CSA Seep Sampling Results.................................................................................41
7.3.3 Comparison of Exceedances to 2B Standards......................................................41
7.3.4 Observed Ranges of 2B Standard COI Concentrations........................................42
7.3.5 Discussion of Results for Constituents without 2B Standards...............................42
7.4 Surface Water Speciation.............................................................................................43
7.5 Leaching Potential of Ash.............................................................................................43
7.6 Constituents of Interest.................................................................................................44
7.6.1 COls in Ash (based on total inorganics analysis, as shown in Table 7-2).............44
7.6.2 COls in Ash Basin Surface Water (based on water quality analysis (totals), as
shownin Table 7-4).............................................................................................................44
7.6.3 COls in Ash Porewater (based on water quality analysis (totals), as shown in
Table7-5)............................................................................................................................45
7.6.4 COls in Seeps (based on water quality analysis (totals), as shown in Table 7-10)
45
7.6.5 Summary of COls from Source Characterization..................................................46
8.0 Soil and Rock Characterization........................................................................................47
8.1 Background Sample Locations.....................................................................................47
8.2 Analytical Methods and Results...................................................................................47
8.3 Comparison of Soil Results to Applicable Levels.........................................................47
8.4 Comparison of Soil Results to Background..................................................................48
8.4.1 Background Soil....................................................................................................48
8.4.2 Soil Beneath Ash Basin.........................................................................................48
8.4.3 Soil Beneath Ash Storage Area.............................................................................48
8.4.4 Soil Outside the Waste Boundary .........................................................................49
8.5 Comparison of PWR and Bedrock Results to Background...........................................49
8.5.1 Background PWR and Bedrock.............................................................................49
8.5.2 PWR and Bedrock Beneath Ash Basin.................................................................49
8.5.3 PWR and Bedrock Beneath Ash Storage Area.....................................................50
8.5.4 PWR and Bedrock Outside Waste Boundary ........................................................50
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9.0 Sediment Characterization...............................................................................................51
9.1 Sediments.....................................................................................................................51
10.0 Groundwater Characterization.........................................................................................52
10.1 Regional Groundwater Data for Constituents of Interest..............................................52
10.1.1 Antimony...............................................................................................................52
10.1.2 Arsenic..................................................................................................................53
10.1.3 Barium...................................................................................................................53
10.1.4 Boron.....................................................................................................................
54
10.1.5 Chromium..............................................................................................................54
10.1.6 Cobalt....................................................................................................................
55
10.1.7 Iron........................................................................................................................55
10.1.8 Manganese............................................................................................................55
10.1.9 Nickel.....................................................................................................................56
10.1.10 Selenium............................................................................................................57
10.1.11 Sulfate................................................................................................................58
10.1.12 TDS....................................................................................................................58
10.1.13 Thallium.............................................................................................................59
10.1.14 Vanadium...........................................................................................................59
10.1.15 pH......................................................................................................................60
10.2 Background Wells.........................................................................................................60
10.3 Discussion of Redox Conditions...................................................................................62
10.4 Groundwater Analytical Results...................................................................................62
10.4.1 Ash Basin..............................................................................................................64
10.4.2 Ash Storage Area..................................................................................................64
10.4.3 Outside the Waste Boundary................................................................................64
10.5 Comparison of Results to 2L Standards and IMACs....................................................65
10.6 Comparison of Results to Background.........................................................................65
10.6.1 Background Wells MW-6S and MW-6D................................................................65
10.6.2 Newly Installed Background Wells........................................................................66
10.6.3 Regional Groundwater Data..................................................................................66
10.6.4 Groundwater Beneath the Ash Basin....................................................................67
10.6.5 Groundwater Beneath the Ash Storage Area........................................................67
10.6.6 Groundwater Beyond the Waste Boundary...........................................................67
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10.7 Cation and Anion Water Quality Data...........................................................................70
10.8 CCR Rule Groundwater Detection and Assessment Monitoring Parameters...............70
11.0 Hydrogeological Investigation..........................................................................................73
11.1 Hydrostratigraphic Layer Development........................................................................73
11.2 Hydrostratigraphic Layer Properties.............................................................................74
11.2.1 Borehole In -Situ Tests...........................................................................................74
11.2.2 Monitoring Well and Observation Well Slug Tests................................................75
11.2.3 Laboratory Permeability Tests...............................................................................76
11.2.4 Hydrostratigraphic Layer Parameters....................................................................76
11.3 Hydraulic Gradients......................................................................................................76
11.4 Groundwater Velocity...................................................................................................77
11.5 Contaminant Velocity....................................................................................................77
11.6 Plume's Physical and Chemical Characterization........................................................77
11.7 Groundwater / Surface Water Interaction.....................................................................80
11.8 Estimated Seasonal High and Seasonal Low Groundwater Elevations — Compliance
andVoluntary Wells................................................................................................................81
12.0 Screening -Level Risk Assessment...................................................................................82
12.1 Human Health Screening.............................................................................................82
12.1.1 Introduction............................................................................................................
82
12.1.2 Conceptual Site Model..........................................................................................83
12.1.3 Human Health Risk -Based Screening Levels.......................................................85
12.1.4 Site -Specific Risk Based Remediation Standards.................................................86
12.1.5 NCDENR Receptor Well Investigation..................................................................86
12.1.6 Human Health Risk Screening Summary ..............................................................86
12.2 Ecological Screening....................................................................................................87
12.2.1 Introduction............................................................................................................
87
12.2.2 Ecological Setting..................................................................................................87
12.2.3 Fate and Transport Mechanisms...........................................................................92
12.2.4 Comparison to Ecological Screening Levels.........................................................92
12.2.5 Uncertainty and Data Gaps...................................................................................94
12.2.6 Scientific/Management Decision Point..................................................................
94
12.2.7 Ecological Risk Screening Summary....................................................................95
13.0 Groundwater Modeling.....................................................................................................96
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13.1 Fate and Transport Groundwater Modeling..................................................................96
13.2
Batch Geochemical Modeling.......................................................................................97
13.3
Geochemical Site Conceptual Site Model....................................................................97
14.0
Data Gaps — SCM Uncertainties....................................................................................100
14.1
Data Gaps..................................................................................................................100
14.1.1 Data Gaps Resulting from Temporal Constraints................................................100
14.1.2 Data Gaps Resulting from Review of Data Obtained During CSA Activities .......
100
14.1.3 Data Gaps Resulting from Other Sources...........................................................101
14.2
Site Heterogeneities...................................................................................................101
14.3
Impact of Data Gaps and Site Heterogeneities..........................................................101
15.0
Planned Sampling for CSA Supplement........................................................................102
15.1
Sampling Plan for Inorganic Constituents..................................................................102
15.2
Sampling Plan for Speciation Constituents................................................................102
16.0
Interim Groundwater Monitoring Plan............................................................................103
16.1
Sampling Frequency...................................................................................................103
16.2
Constituent and Parameter List..................................................................................103
16.3
Proposed Interim Sampling Locations........................................................................103
16.4
Proposed Interim Background Wells..........................................................................103
17.0
Discussion......................................................................................................................104
17.1
Summary of Completed and Ongoing Work...............................................................104
17.2
Nature and Extent of Contamination..........................................................................105
17.2.1 Groundwater and Seep Contamination...............................................................105
17.2.2 Soil, Rock, and Sediment Contamination............................................................106
17.3
Maximum Contaminant Concentrations.....................................................................106
17.4
Contaminant Migration and Potentially Affected Receptors.......................................108
18.0
Conclusions....................................................................................................................109
18.1
Source and Cause of Contamination..........................................................................109
18.2
Imminent Hazards to Public Health and Safety and Actions Taken to Mitigate them in
Accordance to 15A NCAC 02L .0106(f)................................................................................109
18.3
Receptors and Significant Exposure Pathways..........................................................109
18.4
Horizontal and Vertical Extent of Soil and Groundwater Contamination and Significant
Factors Affecting Contaminant Transport..............................................................................109
18.5
Geological and Hydrogeological Features influencing the Movement, Chemical, and
Physical Character of the Contaminants...............................................................................111
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
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TABLE OF CONTENTS
18.6 Proposed Continued Monitoring.................................................................................112
18.7 Preliminary Evaluation of Corrective Action Alternatives............................................112
19.0 References.....................................................................................................................114
Vii
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
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LIST OF FIGURES
List Of Figures (organized by CSA report section)
Executive Summary
• Figure ES-1: Plan View — General Groundwater Flow Direction, Location of
Receptor Wells, Constituent Plume Characterization
1.0 Introduction
<No Figures>
2.0 Site History and Description
• Figure 2-1: Site Location Map
• Figure 2-2: Site Layout Map
• Figure 2-3: Pre -Ash Basin USGS Map
• Figure 2-4: Site Features Map
• Figure 2-5: Site Vicinity Map
• Figure 2-6: Buck Steam Station Flow Schematic Diagram
• Figure 2-7: Compliance and Voluntary Monitoring Wells
3.0 Source Characteristics
• Figure 3-1: Photo of Fly Ash and Bottom Ash
• Figure 3-2: Elemental composition for bottom ash, fly ash, shale, and volcanic ash
• Figure 3-3: Coal Ash TCLP Leachate Concentration vs Regulatory Limits
• Figure 3-4: Trace Elements in Fly Ash vs Soil (EPRI)
• Figure 3-5: Trace Elements in Bottom Ash vs Soil (EPRI)
4.0 Receptor Information
• Figure 4-1: USGS Receptor Map
• Figure 4-2: Receptor Map - Aerial Base
• Figure 4-3: Ash Basin Underground Features
• Figure 4-4: Surface Water Bodies
• Figure 4-5: Properties Contiguous to the Ash Basin Waste Boundary
5.0 Regional Geology and Hydrogeology
• Figure 5-1: Tectonostratigraphic Map of the Southern and Central Appalachians
• Figure 5-2: Regional Geologic Map
• Figure 5-3: Interconnected, Two -Medium Piedmont Groundwater System
• Figure 5-4: Conceptual Variations of the Transition Zone due to Rock Type and
Structure
• Figure 5-5: Piedmont Slope -Aquifer System
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
Buck Steam Station Ash Basin
LIST OF FIGURES
6.0 Site Geology and Hydrogeology
• Figure 6-1: Site Geologic Map
• Figure 6-2: Monitoring Well and Sample Locations
• Figure 6-3: Topographic Lineaments and Rose Diagram
• Figure 6-4: Aerial Photography Lineaments and Rose Diagram
• Figure 6-5: Water Table Surface - Shallow Wells (S) (7/6 & 7, 2015)
• Figure 6-6: Potentiometric Surface - Deep Wells (D) (7/6 & 7, 2015)
• Figure 6-7: Potentiometric Surface - BR - Bedrock Groundwater Elevations (7/6 & 7,
2015)
7.0 Source Characterization
Figure 7-1: Source Characterization Sample Location
8.0 Soil and Rock Characterization
• Figure 8-1: Soil Analytical Results — Plan View (PSRG Exceedances)
• Figure 8-2.1: Cross Section A -A' with Solid Matrix Analytical Results
• Figure 8-2.2: Cross Section A -A' with Solid Matrix Analytical Results
• Figure 8-3: Cross Section B-B' with Solid Matrix Analytical Results
• Figure 8-4: Cross Section C-C' with Solid Matrix Analytical Results
9.0 Surface Water and Sediment Characterization
• Figure 9-1: Seep and Surface Water Sample Locations (show NPDES seeps)
• Figure 9-2: NCDENR March 2014 Sample Location
10.0 Groundwater Characterization
• Figure 10-1: Arsenic Concentrations in Groundwater
• Figure 10-2: Iron Concentrations in Groundwater
• Figure 10-3: Regional Groundwater Quality - Manganese
• Figure 10-4: Regional Groundwater Quality
• Figure 10-5: Thallium Distribution in Soil
• Figure 10-6: Regional Groundwater Quality - Vanadium
• Figure 10-7: Monitoring Well and Sample Locations
• Figure 10-8: Typical Well Construction Details
• Figure 10-9: Groundwater Analytical Results — Plan View (21- and IMAC Standard
Exceedances)
• Figure 10-10: Antimony Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-11: Antimony Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-12: Antimony Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-13: Arsenic Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-14: Arsenic Isoconcentration Contour Map — Shallow Aquifer (D Wells)
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
Buck Steam Station Ash Basin
LIST OF FIGURES
• Figure 10-15: Arsenic Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-16: Barium Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-17: Barium Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-18: Barium Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-19: Boron Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-20: Boron Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-21: Boron Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-22: Chromium Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-23: Chromium Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-24: Chromium Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-25: Cobalt Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-26: Cobalt Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-27: Cobalt Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-28: Iron Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-29: Iron Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-30: Iron Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-31: Manganese Isoconcentration Contour Map — Shallow Aquifer (S
Wells)
• Figure 10-32: Manganese Isoconcentration Contour Map — Shallow Aquifer (D
Wells)
• Figure 10-33: Manganese Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-34: Nickel Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-35: Nickel Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-36: Nickel Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-37: Selenium Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-38: Selenium Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-39: Selenium Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-40: Sulfate Isoconcentration Contour Map — Shallow Aquifer (S Wells)
• Figure 10-41: Sulfate Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-42: Sulfate Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-43: Thallium Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-44: Thallium Isoconcentration Contour — Shallow Aquifer (S Wells)
• Figure 10-45: Thallium Isoconcentration Contour — Shallow Aquifer (D Wells)
• Figure 10-46: Total Dissolved Solids Isoconcentration Contour Map — Shallow
Aquifer (S Wells)
• Figure 10-47: Total Dissolved Solids Isoconcentration Contour Map — Shallow
Aquifer (D Wells)
• Figure 10-48: Total Dissolved Solids Isoconcentration Contour — Deep Aquifer (BR
Wells)
• Figure 10-49: Vanadium Isoconcentration Contour Map — Shallow Aquifer (S Wells)
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
Buck Steam Station Ash Basin
LIST OF FIGURES
• Figure 10-50: Vanadium Isoconcentration Contour Map — Shallow Aquifer (D Wells)
• Figure 10-51: Vanadium Isoconcentration Contour Map — Deep Aquifer (BR Wells)
• Figure 10-52: Cross Section A -A' with Groundwater Analytical Results
• Figure 10-53: Cross Section A -A' with Groundwater Analytical Results
• Figure 10-54: Cross Section B-B' with Groundwater Analytical Results
• Figure 10-55: Cross Section C-C' with Groundwater Analytical Results
• Figure 10-56: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Background Monitoring Wells
• Figure 10-57: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Seeps
• Figure 10-58: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Downgradient Shallow (S) Monitoring Wells
• Figure 10-59: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Downgradient Deep (D) Monitoring Wells
• Figure 10-60: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Downgradient Upper Bedrock (BRU) Monitoring Wells
• Figure 10-61: Piper Diagram — Ash Basin Porewater and Ash Basin Surface Water
and Downgradient Bedrock (BR) Wells
• Figure 10-62: Piper Diagram — Background Shallow (S) Monitoring Wells with
Downgradient Shallow (S) Monitoring Wells
• Figure 10-63: Piper Diagram — Background Deep (D) Monitoring Wells with
Downgradient Deep (D) Monitoring Wells
• Figure 10-64: Cation/Anion Concentrations (bar chart) — Ash basin porewater
• Figure 10-65: Cation/Anion Concentrations (bar chart) — Ash basin surface water
• Figure 10-66: Cation/Anion Concentrations (bar chart) — Background wells
• Figure 10-67: Cation/Anion Concentrations (bar chart) — Seep wells
• Figure 10-68: Cation/Anion Concentrations (bar chart) — Downgradient S (1 of 2)
• Figure 10-69: Cation/Anion Concentrations (bar chart) — Downgradient S (2 of 2)
• Figure 10-70: Cation/Anion Concentrations (bar chart) — Downgradient D (1 of 2)
• Figure 10-71: Cation/Anion Concentrations (bar chart) — Downgradient D (2 of 2)
• Figure 10-72: Cation/Anion Concentrations (bar chart) — Downgradient BRU
• Figure 10-73: Cation/Anion Concentrations (bar chart) — Downgradient BR
• Figure 10-74: Sulfate:Chloride Ratio in Ash basin porewater
• Figure 10-75:
Sulfate:Chloride Ratio in Ash basin surface water
• Figure 10-76:
Sulfate:Chloride Ratio in Background well
• Figure 10-77:
Sulfate:Chloride Ratio in Seep well
• Figure 10-78:
Sulfate:Chloride Ratio in Downgradient S well (1 of 2)
• Figure 10-79:
Sulfate:Chloride Ratio in Downgradient S well (2 of 2)
• Figure 10-80:
Sulfate: Chloride Ratio in Downgradient D well (1 of 2)
• Figure 10-81:
Sulfate:Chloride Ratio in Downgradient D well (2 of 2)
• Figure 10-82:
Sulfate:Chloride Ratio in Downgradient BRU well
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF FIGURES
• Figure 10-83: Sulfate:Chloride Ratio in Downgradient BR well
• Figure 10-84: Stacked Time Series Plot: Boron
• Figure 10-85: Stacked Time Series Plot: Chromium
• Figure 10-86: Stacked Time Series Plot: Iron
• Figure 10-87: Stacked Time Series Plot: Manganese
• Figure 10-88: Stacked Time Series Plot: pH
• Figure 10-89: Stacked Time Series Plot: Sulfate
• Figure 10-90: Stacked Time Series Plot: TDS
• Figure 10-91: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: Boron
• Figure 10-92: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: Chromium
• Figure 10-93: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: Iron
• Figure 10-94: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: Manganese
• Figure 10-95: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: Sulfate
• Figure 10-96: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: pH
• Figure 10-97: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6D) vs Deep wells: TDS
• Figure 10-98: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6S) vs Shallow wells: Boron
• Figure 10-99: Stacked Time Series Plot: Compliance Wells — Background well (MW-
6S) vs Shallow wells: Chromium
• Figure 10-100: Stacked Time Series Plot: Compliance Wells — Background well
(MW-6S) vs Shallow wells: Iron (tot)
• Figure 10-101: Stacked Time Series Plot: Compliance Wells — Background well
(MW-6S) vs Shallow wells: Manganese
• Figure 10-102: Stacked Time Series Plot: Compliance Wells — Background well
(MW-6S) vs Shallow wells: pH
• Figure 10-103: Stacked Time Series Plot: Compliance Wells — Background well
(MW-6S) vs Shallow wells: Sulfate
• Figure 10-104: Stacked Time Series Plot: Compliance Wells — Background well
(MW-6S) vs Shallow wells: TDS
• Figure 10-105: Stacked Time Series Plot: Boron vs Turbidity: MW — 11 D
• Figure 10-106: Stacked Time Series Plot: Chromium vs Turbidity: MW-12S
• Figure 10-107: Stacked Time Series Plot: Iron vs Turbidity: MW-6S
• Figure 10-108: Stacked Time Series Plot: Iron vs Turbidity: MW-7D
• Figure 10-109: Stacked Time Series Plot: Iron vs Turbidity: MW-8S
• Figure 10-110: Stacked Time Series Plot: Iron vs Turbidity: MW-8D
xii
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
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LIST OF FIGURES
• Figure 10-111: Stacked Time Series Plot: Iron vs Turbidity: MW-9S
• Figure 10-112: Stacked Time Series Plot: Iron vs Turbidity: MW-9D
• Figure 10-113: Stacked Time Series Plot: Iron vs Turbidity: MW-10D
• Figure 10-114: Stacked Time Series Plot: Iron vs Turbidity: MW-11S
• Figure 10-115: Stacked Time Series Plot: Iron vs Turbidity: MW-11 D
• Figure 10-116: Stacked Time Series Plot: Iron vs Turbidity: MW-12S
• Figure 10-117: Stacked Time Series Plot: Iron vs Turbidity: MW-12D
• Figure 10-118: Stacked Time Series Plot: Iron vs Turbidity: MW-13D
• Figure 10-119: Stacked Time Series Plot: Manganese vs Turbidity: MW-6S
• Figure 10-120: Stacked Time Series Plot: Manganese vs Turbidity: MW-7S
• Figure 10-121: Stacked Time Series Plot: Manganese vs Turbidity: MW-7D
• Figure 10-122: Stacked Time Series Plot: Manganese vs Turbidity: MW-8S
• Figure 10-123: Stacked Time Series Plot: Manganese vs Turbidity: MW-9S
• Figure 10-124: Stacked Time Series Plot: Manganese vs Turbidity: MW-10D
• Figure 10-125: Stacked Time Series Plot: Manganese vs Turbidity: MW-11 S
• Figure 10-126: Stacked Time Series Plot: Manganese vs Turbidity: MW-11 D
• Figure 10-127: Stacked Time Series Plot: Manganese vs Turbidity: MW-12S
• Figure 10-128: Stacked Time Series Plot: pH vs Turbidity: MW-6S
• Figure 10-129: Stacked Time Series Plot: pH vs Turbidity: MW-6D
• Figure 10-130: Stacked Time Series Plot: pH vs Turbidity: MW-7S
• Figure 10-131: Stacked Time Series Plot: pH vs Turbidity: MW-7D
• Figure 10-132: Stacked Time Series Plot: pH vs Turbidity: MW-8S
• Figure 10-133: Stacked Time Series Plot: pH vs Turbidity: MW-8D
• Figure 10-134: Stacked Time Series Plot: pH vs Turbidity: MW-9S
• Figure 10-135: Stacked Time Series Plot: pH vs Turbidity: MW-9D
• Figure 10-136: Stacked Time Series Plot: pH vs Turbidity: MW-10D
• Figure 10-137: Stacked Time Series Plot: pH vs Turbidity: MW-11 S
• Figure 10-138: Stacked Time Series Plot: pH vs Turbidity: MW-11 D
• Figure 10-139: Stacked Time Series Plot: pH vs Turbidity: MW-12S
• Figure 10-140: Stacked Time Series Plot: pH vs Turbidity: MW-12D
• Figure 10-141: Stacked Time Series Plot: pH vs Turbidity: MW-13D
• Figure 10-142: Stacked Time Series Plot: TDS vs Turbidity: MW-10D
• Figure 10-143: 40 CFR 257 Appendix III Detection Monitoring Constituents
Detected in Shallow Wells
• Figure 10-144: 40 CFR 257 Appendix III Detection Monitoring Constituents
Detected in Deep Wells
• Figure 10-145: 40 CFR 257 Appendix III Constituents Detected in Bedrock Wells
• Figure 10-146: 40 CFR 257 Appendix IV Assessment Monitoring Constituents
Detected in Shallow
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF FIGURES
• Figure 10-147: 40 CFR 257 Appendix IV Assessment Monitoring Constituents
Detected in Deep Wells
• Figure 10-148: 40 CFR 257 Appendix IV Assessment Monitoring Constituents
Detected in Bedrock Wells
11.0 HydrogeologicalInvestigation
• Figure 11-1: Major Flow Transects
12.0 Screening -Level Risk Assessment
• Figure 12-1: Human Health Screening Conceptual Site Model
• Figure 12-2: Ecological Conceptual Site Model
13.0 Groundwater Modeling
<No Figures>
14.0 Data Gaps — Conceptual Site Model Uncertainties
<No Figures>
15.0 Planned Sampling for CSA Supplement
<No Figures>
16.0 Interim Groundwater Monitoring Plan
<No Figures>
17.0 Discussion
<No Figures>
18.0 Conclusions
<No Figures>
19.0 References
<No Figures>
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF TABLES
List Of Tables (organized by CSA report section)
Executive Summary
<No Tables>
1.0 Introduction
• Table 1-1: Comparison of Sampling Data to Federal and State Regulatory
Standards
2.0 Site History and Description
• Table 2-1: NPDES Groundwater Monitoring Requirements
• Table 2-2: Exceedances of 2L Standards at Compliance Wells (March 2011-March
2015)
• Table 2-3: Summary of Onsite Environmental Incidents
3.0 Source Characteristics
• Table 3-1: Range (10th percentile — 90th percentile) in Bulk Composition of Fly Ash,
Bottom Ash, Rock, and Soil
4.0 Receptor Information
• Table 4-1: Public and Private Water Supply Well Information within 0.5-mile Radius
of Ash Basin Compliance Boundary
• Table 4-2: Property Owner Addresses Contiguous to the Ash Basin Waste Boundary
5.0 Regional Geology and Hydrogeology
<No Tables>
6.0 Site Geology and Hydrogeology
• Table 6-1: Soil Mineralogy Results
• Table 6-2: Soil Chemistry Results, Oxides
• Table 6-3: Soil Chemistry Results, Elemental
• Table 6-4: Transition Zone Mineralogy
• Table 6-5: Oxide Composition of Transitional Zone Samples
• Table 6-6: Elemental Composition of Transitional Zone Samples
• Table 6-7: Whole Rock Chemistry Results, Oxides.xlsx
• Table 6-8: Whole Rock Chemistry Results, Elemental
• Table 6-9: Assessment Monitoring Well Construction Information
• Table:6-10: Compliance and Voluntary Monitoring Well Construction Information
• Table 6-11: Summary of Hydraulic Gradient Calculations
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Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
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LIST OF TABLES
7.0 Source Characterization
• Table 7-1: Soil and Ash Parameters and Analytical Methods
• Table 7-2: Ash Sample Results
• Table 7-3: Ash Basin Surface Water, Porewater and Seep Parameters and Analytical
Methods
• Table 7-4: Ash Basin Surface Water Sample Results
• Table 7-5: Ash Basin Porewater Sample Results
• Table 7-6: Ash Sample SPLP Results
• Table 7-7: Ash Basin Porewater Sample Results - Speciation
• Table 7-8; Groundwater Radiological Sample Results
• Table 7-9: NCDENR March 2014 Sampling Results
• Table 7-10: Seep Sample Results
• Table 7-11: Surface Water Sample Results - Speciation
8.0 Soil and Rock Characterization
• Table 8-1: Environmental Exploration and Sampling Plan
• Table 8-2: Solid and Ash Parameters and Analytical Methods
• Table 8-3: Total Inorganic Results — Background Soil
• Table 8-4: Total Inorganic Results — Background PWR and Bedrock
• Table 8-5: Total Inorganic Results - Soil
• Table 8-6: Total Inorganic Results - PWR and Bedrock
• Table 8-7: Frequency and Concentration Ranges in Soil for COI Exceedances of
North Carolina PSRGs
• Table 8-8: Frequency and Concentration Ranges in PWR and Bedrock for COI
Exceedances of North Carolina PSRGs
• Table 8-9: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — Soil Beneath Ash Basin
• Table 8-10: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — Soil Beneath Ash Storage Area
• Table 8-11: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — Soil Outside the Waste Boundary
• Table 8-12: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — PWR and Bedrock Beneath Ash Basin
• Table 8-13: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — PWR and Bedrock Beneath Ash Storage
Area
• Table 8-14: Range of Constituent Concentrations and Comparison to Range of
Reported Background Concentrations — PWR and Bedrock Outside of Waste
Boundary
9.0 Surface Water and Sediment Characterization
0 Table 9-1: Total Inorganic Results - Sediment
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
Buck Steam Station Ash Basin
LIST OF TABLES
10.0 Groundwater Characterization
• Table 10-1: State and Federal Drinking Water Standards
• Table 10-2: Constituents in Private Wells
• Table 10-3: Iron and Manganese Concentrations
• Table 10-4: Redox Conditions — General Redox Category
• Table 10-5: Groundwater Sample Results — Background — Total and Dissolved
• Table 10-6: Groundwater Sample Results — Total and Dissolved
• Table 10-7: Groundwater Sample Results — Background — Speciation
• Table 10-8: Groundwater Sample Results — Speciation
• Table 10-9: Range of COI Concentrations in Groundwater Beneath the Ash Basin
• Table 10-10: Range of COI Concentrations in Groundwater Beneath the Ash
Storage Area
• Table 10-11: Range of COI Concentrations in Groundwater Outside the Waste
Boundary
11.0 HydrogeologicalInvestigation
• Table 11-1: Soil/Material Properties for Ash, Fill, Alluvium, Soil/Saprolite
• Table 11-2: Field Permeability Test Results
• Table 11-3: Slug Test Permeability Results
• Table 11-4: Historic Slug Test Permeability Results
• Table 11-5: Laboratory Permeability Test Results
• Table 11-6: Historic Laboratory Permeability Test Results
• Table 11-7: Total Porosity for Upper Hydrostratigraphic Units (A, F, S, M1, and M2)
• Table 11-8: Estimated Effective Porosity/Specific Yield and Specific Storage for
Upper Hydrostratigraphic Units (A, F, S, M1, and M2)
• Table 11-9: Hydrostratigraphic Layer Properties — Horizontal Hydraulic Conductivity
• Table 11-10: Hydrostratigraphic Layer Properties — Vertical Hydraulic Conductivity
• Table 11-11: Total Porosity, Secondary (Effective) Porosity/Specific Yield, and
Specific Storage for Lower Hydrostratigraphic Units (TZ and BR)
• Table 11-12: Groundwater Seepage Velocities
• Table 11-13: Hydraulic Gradients — Vertical
12.0 Screening -Level Risk Assessment
• Table 12-1: Selection of Human Health COPCs — Groundwater
• Table 12-2: Selection of Human Health COPCs — Soil
• Table 12-3: Selection of Human Health COPCs — Sediment
• Table 12-4: Contaminants of Potential Human Health Concern
• Table 12-5: Selection of Ecological COPCs — Soil
• Table 12-6: Selection of Ecological COPCs — Sediment
• Table 12-7: Contaminants of Potential Ecological Concern
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF TABLES
Table 12-8: Threatened and Endangered Species in Rowan County
13.0 Groundwater Modeling
<No Tables>
14.0 Data Gaps — Conceptual Site Model Uncertainties
<No Tables>
15.0 Planned Sampling for CSA Supplement
• Table 15-1: CSA Supplemental Sampling Plan
16.0 Interim Groundwater Montoring Plan
• Table 16-1: Recommended Parameters and Constituents
• Table 16-2: Sample Locations in Interim Groundwater Monitoring Plan
17.0 Discussion
<No Tables>
18.0 Conclusions
<No Tables>
19.0 References
<No Tables>
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report ��
Buck Steam Station Ash Basin
LIST OF APPENDICES
List of Appendices
Appendix A: Introduction
• NCDENR NORR Letter
• Summary of Work Plan Submittals and NCDENR-Duke Energy Correspondence
• Revised Groundwater Assessment Work Plan
Appendix B: Receptor Information
• Updated Receptor Survey Report
• NCDENR Well Water Sampling Results
• NCDENR Water Supply Well Tracking Spreadsheet
• Background Water Supply Well Analytical Results
Appendix C: Source Characterization
• Drilling Procedures
• Drilling and Installation Variances
Appendix D: Soil and Rock Characterization
• Sampling Procedures
• Sampling Variances
Appendix E: Field and Sampling Quality Control / Quality Assurance
• Field Sampling Quality Assurance/Quality Control Procedures
• Data Analysis Quality Assurance/Quality Control Procedures
Appendix F: Surface Water, Seep and Sediment Characterization
• Sampling Procedures
• Sampling Variances
Appendix G: Groundwater Characterization
• Well Development Procedure
• Well Development Forms
• Well Abandonment Forms
• Sampling Procedures
• Sampling Forms
• Sampling Variances
• Evaluation of Turbidity in Existing Voluntary and Compliance Wells
• Evaluation of Need for Off -site Monitoring Wells
• Statistical Analysis of Groundwater Results
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF APPENDICES
Appendix H: Hydrogeological Investigation
• Boring Logs
• Well Construction Records
• Historical Boring Logs and Well Construction Records
• Soil Physical Lab Reports
• Mineralogy Lab Reports
• Slug Test Procedures
• Slug Test Reports
• Field Permeability Data
• Fetter -Bear Diagrams — Porosity
• Estimated Seasonal High Groundwater Elevations Calculation
Appendix I: Screening -Level Risk Assessment
• Trustee Letters and Responses
• Checklist for Ecological Assessments/Sampling
Appendix J: Historical Analytical Result Tables
Appendix K: Laboratory Reports (Compact Disc)
Appendix L: Soil Sample and Rock Core Photographs
Appendix M: CSA Certification Form
Duke Energy Carolinas, LLC I Comprehensive Site Assessment Report
Buck Steam Station Ash Basin FN
LIST OF ACRONYMS AND ABBREVIATIONS
List of Acronyms and Abbreviations
pg/L micrograms per liter
2L Standards 15A NCAC 02L .0202 Groundwater Quality Standards
AMEC
AMEC Environment & Infrastructure
AST
Aboveground Storage Tank
ASTM
American Society for Testing and Materials
BG
Background
bgs
Below ground surface
BR
Bedrock
Buck
Buck Steam Station
CAMA
Coal Ash Management Act
CAP
Corrective Action Plan
CCR
Coal Combustion Residuals
COI
Constituent of Interest
COPC
Contaminant of Potential Concern
CSA
Comprehensive Site Assessment
CSM
Conceptual Site Model
CY
Cubic Yards
DEH
NCDENR Department of Environmental Health
DO
Dissolved oxygen
DORS
Distribution of Residuals Solids
DTW
Depth to Water
Duke Energy
Duke Energy Carolinas, LLC
DWR
NCDENR Division of Water Resources
EDR
Environmental Data Resources
EPD
Georgia Environmental Protection Division
EPRI
Electric Power Research Institute
ESH
Estimated Seasonal High
ESL
Estimated Seasonal Low
GSCM
Geochemical Site conceptual model
GIS
Geographic Information Systems
HFO
Hydrous ferric oxide
HQ
Hazard Quotient
IMAC
Interim Maximum Allowable Concentration
Kd
Sorption Coefficient
MCL
Maximum Contaminant Levels
mD
millidarcies
MDL
Method detection limit
XXI
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LIST OF ACRONYMS AND ABBREVIATIONS
mg/kg
Milligrams per kilogram
mm
milligrams
MNA
Monitored Natural Attenuation
MRL
Maximum Reporting Level
MW
Megawatt
N
Standard Penetration Testing Values
NRCS
Natural Resources Conservation Service
NCAC
North Carolina Administrative Code
NCDENR
North Carolina Department of Environment and Natural Resources
NCDHHS
North Carolina Department of Health and Human Services
NCNHP
North Carolina Natural Heritage Program
NCWRC
North Carolina Wildlife Resources Commission
ng/L
Nanograms per liter
NHD
USGS National Hydrography Dataset
NORR
Notice of Regulatory Requirements
NPDES
National Pollutant Discharge Elimination System
NTU
Nephelometric Turbidity Unit
INURE
National Uranium Resource Evaluation
PL
Prediction Limit
PMCL
Primary Maximum Contaminant Level
ppb
parts per billion
ppm
parts per million
PSRG
Preliminary Soil Remediation Goal
PWR
Partially Weathered Rock
PWSS
NCDENR DWR Public Water Supply Section
RCRA
Resource Conservation and Recovery Act
REC
Recovery
RL
Reporting Limit
RQD
Rock Quality Designation
RSL
USEPA Regional Screening Level
SCM
Site Conceptual Model
SCS
U.S. Department of Agriculture Soil Conservation Service
SLERA
Screening Level Ecological Risk Assessment
SMCL
Secondary Maximum Contaminant Level
SMDP
Scientific/Management Decision Point
SPLP
Synthetic Precipitation Leaching Procedure
SQL
Sample Quantitation Limit
SWAP
NCDENR DWR Source Water Assessment Program
TCLP
Toxicity Characteristic Leaching Procedure
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LIST OF ACRONYMS AND ABBREVIATIONS
TDS
Total Dissolved Solids
TZ
Transition Zone
UNC
University of North Carolina
UNCC
University of North Carolina at Charlotte
USCS
Unified Soil Classification System
USDA
U.S. Department of Agriculture
USEPA
U.S. Environmental Protection Agency
USGS
U.S. Geological Survey
UST
Underground Storage Tank
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1.0 INTRODUCTION
1.0 Introduction
Duke Energy Carolinas, LLC (Duke Energy) owns and formerly operated the Buck Steam
Station (Buck), located on the Yadkin River in Rowan County near Salisbury, North Carolina.
Buck began operation in 1926 as a coal-fired generating station. The Buck Combined Cycle
Station (BCCS) natural gas facility was constructed at the site and began operating in late 2011.
Subsequently, Buck was decommissioned and taken offline in April 2013. The coal ash residue
from Buck's coal combustion process was historically disposed of in the station's ash basin
located adjacent to the station and the Yadkin River. The entire site includes Buck, BCCS, the
ash basin (which consists of three cells), and an ash storage area.
Duke Energy has implemented voluntary and National Pollutant Discharge Elimination System
(NPDES) permit -required compliance groundwater monitoring at Buck. Twice per year voluntary
groundwater monitoring around the Buck ash basin was performed from November 2006 until
May 2010, with analytical results submitted to the North Carolina Department of Environment
and Natural Resources (NCDENR) Division of Water Resources (DWR). Compliance
groundwater monitoring, required by the NPDES permit, began in March 2011. From March
2011 through July 2015, the compliance groundwater monitoring wells at Buck have been
sampled a total of 14 times as part of three times per year sampling required in the NPDES
permit and have been submitted to DWR.
Recent monitoring events have indicated exceedances of 15A NCAC 02L .0200 Groundwater
Quality Standards (2L Standards) at Buck, prompting NCDENR's requirement for Duke Energy
to perform a groundwater assessment at the site and prepare a Comprehensive Site
Assessment (CSA) report. The Coal Ash Management Act of 2014 (CAMA), NC Session Law
2014-122, also directed owners of coal combustion residuals (CCR) surface impoundments to
conduct groundwater monitoring and assessment and submit a Groundwater Assessment
Report. This CSA is submitted to meet the requirements of both NCDENR and CAMA.
1.1 Purpose of Comprehensive Site Assessment
The purpose of this CSA is to characterize the extent of contamination resulting from historical
production and storage of coal ash, evaluate the chemical and physical characteristics of the
contaminants, investigate the geology and hydrogeology of the site including factors relating to
contaminant transport, and examine risk to potential receptors and exposure pathways. This
CSA was prepared in general accordance with requirements outlined in the following regulations
and documents:
• Groundwater Classifications and Water Quality Standards, 15A NCAC Subchapter 2L;
• Coal Ash Management Act of 2014, N.C. Gen.Stat. §§130A-309.200 et seq.;
• Notice of Regulatory Requirements (NORR) issued by NCDENR on August 13, 2014;
• Conditional Approval of Revised Groundwater Assessment Work Plan issued by
NCDENR on February 24, 2015; and
• Subsequent meetings and correspondence between Duke Energy and NCDENR.
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1.0 INTRODUCTION
Constituents in groundwater were compared to the 2L Standards or Interim Maximum Allowable
Concentrations (IMACs) established by NCDENR pursuant to 15A NCAC 2L.0202(c). The
IMACs were issued in 2010, 2011 and 2012; however, NCDENR has not established a 2L
Standard for these constituents as described in 15A NCAC 2L.0202(c). For this reason, the
IMACs noted in this report are for reference only.
This assessment includes evaluation of possible impacts from the ash basins and related ash
storage facilities, and consisted of the following activities:
• Completion of soil borings, installation of groundwater monitoring wells and collection of
seep samples to faciliatate collection and analysis of chemical, physical, and
hydrogeological parameters of subsurface materials encountered within and beyond the
waste and compliance boundaries;
• Evaluation of testing data to supplement the site conceptual model (SCM);
• Update of the receptor survey previously completed in 2014; and
• Completion of a screening -level risk assessment.
For this CSA, the source area is defined as the ash basin and ash storage area. Source
characterization was performed through the completion of soil borings, installation of monitoring
wells, and collection and analysis of associated solid matrix and aqueous samples to identify
physical and chemical properties of ash, ash basin surface water, ash porewater, and ash basin
seeps. The ash, ash basin surface water, ash porewater, and seep analytical results were
compared to 2L Standards, IMACs, and other regulatory screening levels for the purpose of
identifying constituents of interest (COls). These COls are considered to be associated with
potential impacts to soil and groundwater from the ash basin and storage area.
In addition, this CSA also identifies constituents that exceeded 2L Standards or IMACs from
groundwater sample locations outside the ash basin boundary. For the purposes of this report,
these constituents were also identified as COls. It is important to recognize that certain COls
(e.g., iron and manganese) may be naturally occurring and may be found in background
monitoring wells and thus require careful examination to determine whether their presence near
or downgradient of the ash basin or ash storage areas is a naturally occurring condition or a
result of ash handling and storage. Occurrences of Cols outside the waste boundary are
identified in Sections 10.0 (Groundwater Characterization) and 11.0 (Hydrogeological
Investigation) of this CSA. This inclusive approach to identification of Cols will be refined during
development of the CAP to focus on those constituents that are attributable to the ash basin.
COls were also evaluated in the human health and ecological screening level risk assessment
in Section 12.0.
1.2 Regulatory Background
1.2.1 NCDENR Requirements
The NCDENR DWR regulates wastewater discharges from coal ash ponds to state waters,
streams, and lakes, and requires groundwater monitoring and stormwater management at these
facilities. The agency also has regulatory responsibility for facilities that contain fly and bottom
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1.0 INTRODUCTION
ash from coal burning power operations. Duke Energy's coal-fired power facilities are also
regulated through federal NPDES wastewater permits. As part of these permits, the facilities
must also comply with the state water quality standards and U.S. Environmental Protection
Agency (USEPA) water quality criteria.
Groundwater monitoring is performed at Duke Energy facilities in accordance with approved
monitoring plans and NPDES permits for each site. Included in these monitoring evaluations is a
determination if site -specific background concentrations (i.e., naturally occurring constituents in
the soil profile and groundwater) for various constituents are contributing to reported
concentrations. For each facility, if it is determined that activities on the property are causing
noncompliance with NCDENR regulatory requirements, the agency will require the permittee to
perform an assessment and to develop and implement a Corrective Action Plan (CAP) in
accordance with state regulations.
1.2.2 Notice of Regulatory Requirements
On August 13, 2014, NCDENR issued a Notice of Regulatory Requirements (NORR) letter
notifying Duke Energy that exceedances of the 2L Standards were reported at 14 coal ash
facilities owned and operated by Duke Energy, including Buck. The NORR stipulated that for
each ash facility, Duke Energy shall conduct a CSA following submittal of a Groundwater
Assessment Work Plan (Work Plan) and receptor survey. In accordance with the NORR
requirements, a Work Plan was developed, a receptor survey was performed to identify all
receptors within a 0.5-mile radius (2,640 feet) of the Buck ash basin compliance boundary, and
a CSA was conducted for each coal ash facility. The NORR letter is included as Appendix A.
1.2.3 Coal Ash Management Act Requirements
The Coal Ash Management Act (CAMA) of 2014 (N.C. Gen. Stat. §130A-309.200 et seq.)
requires that coal combustion residuals (CCRs) in high priority impoundments be removed and
disposed in a landfill, used in a structural fill, or used for beneficial reuse. As a component of
implementing this objective, CAMA provides instructions for owners of CCR surface
impoundments to perform various groundwater monitoring and assessment activities. Section
§1 30A-309.21 1 of CAMA specifies groundwater assessment and corrective actions, drinking
water supply well surveys and provisions of alternate water supply, and reporting requirements
as follows:
(a) Groundwater Assessment of Coal Combustion Residuals Surface Impoundments.
— The owner of a coal combustion residuals surface impoundment shall conduct
groundwater monitoring and assessment as provided in this subsection. The
requirements for groundwater monitoring and assessment set out in this
subsection are in addition to any other groundwater monitoring and assessment
requirements applicable to the owners of coal combustion residuals surface
impoundments.
(1) No later than December 31, 2014, the owner of a coal combustion residuals
surface impoundment shall submit a proposed Groundwater Assessment
Plan for the impoundment to the Department for its review and approval. The
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1.0 INTRODUCTION
Groundwater Assessment Plan shall, at a minimum, provide for all of the
following:
a. A description of all receptors and significant exposure pathways.
b. An assessment of the horizontal and vertical extent of soil and
groundwater contamination for all contaminants confirmed to be present
in groundwater in exceedance of groundwater quality standards.
c. A description of all significant factors affecting movement and transport
of contaminants.
d. A description of the geological and hydrogeological features influencing
the chemical and physical character of the contaminants.
e. A schedule for conitnued groundwater monitoring.
f. Any other information related to groundwater assessment required by the
Department.
2) The Department shall approve the Groundwater Assessment Plan if it
determines that the Plan complies with the requirements of this subsection
and will be sufficient to protect public health, safety, and welfare; the
environment; and natural resources.
(3) No later than 10 days from approval of the Groundwater Assessment Plan,
the owner shall begin implementation of the Plan.
(4) No later than 180 days from approval of the Groundwater Assessment Plan,
the owner shall submit a Groundwater Assessment Report to the Department.
The Report shall describe all exceedances of groundwater quality standards
associated with the impoundment.
1.3 NCDENR-Duke Energy Correspondence
In response to both the NORR letter and CAMA requirements, Duke Energy submitted a Work
Plan to NCDENR DWR on September 25, 2014 establishing proposed site assessment
activities and schedules for the implementation, completion, and submission of a CSA report in
accordance with 15A NCAC 02L .0106(g). NCDENR DWR reviewed the Work Plan and
provided Duke Energy with initial comments on November 4, 2014. A revised Work Plan was
subsequently submitted to NCDENR DWR on December 30, 2014 and NCDENR DWR
provided final comments and conditional approval of the revised Work Plan on February 24,
2015. In addition, Duke Energy submitted proposed adjustments to the CSA guideline and
requested clarifications regarding groundwater sampling and speciation of selected constituents
to NCDENR DWR on May 14 and May 22, 2015. NCDENR DWR provided responses to these
proposed revisions and clarifications in June 2015. Copies of relevant correspondence including
Work Plan submittals are included in Appendix A.
1.4 Approach to Comprehensive Site Assessment
The CSA approach was developed based on the NORR guidelines and CAMA requirements.
Development of the SCM is based on several documents including but not limited to USEPA's
Monitored Natural Attenuation tiered approach, ASTM 1689-95 (2014) Standard Guide for
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1.0 INTRODUCTION
Developing Site Conceptual Models for Contaminated Sites, and comments received by
NCDENR.
1.4.1 NORR Guidance
The NORR letter (Appendix A) outlined general guidelines for the CSA report, including
guidance from 15A NCAC 02L .0106(g) as described in Section 1.1. The NORR letter also
included Guidelines for Comprehensive Site Assessment for those involved in the investigation
of contaminated soil and/or groundwater. The components included in the NORR guidelines
were used in developing the site Work Plan and this CSA report.
1.4.2 USEPA Monitored Natural Attenuation Approach
In accordance with NCDENR requirements and the February 16, 2015 Conditional Approval
letter (Appendix A), the elements of the USEPA's Monitored Natural Attenuation (MNA) tiered
approach has been utilized as part of the investigation associated with the CSA. This approach
is described in its guidance document entitled "Monitored Natural Attenuation of Inorganic
Contaminants in Groundwater" (Vols. 1 & 2) (October 2007). MNA may be used as a
component to meet corrective action requirements if site conditions meet the requirements
associated with use of MNA. The approach involves a detailed analysis of site characteristics
controlling and sustaining attenuation to support evaluation and selection of MNA as part of a
cleanup action for inorganic contaminant plumes in groundwater (USEPA 2007). The site
characterization is conducted in a step -wise manner to facilitate collection of data necessary to
progressively evaluate the effectiveness of natural attenuation processes within the site
aquifer(s). Four general elements are included in the tiered site analysis approach:
• Demonstration of active contaminant removal from groundwater and dissolved plume
stability;
• Determination of the mechanism and rate of attenuation;
• Determination of the long-term capacity for attenuation and stability of immobilized
contaminants, before, during, and after any proposed remedial activities; and
• Design of performance monitoring program, including defining triggers for assessing the
remedial action strategy failure, and establishing a contingency plan.
Duke Energy will evaluate the USEPA MNA approach further during preparation of the CAP.
1.4.3 ASTM Conceptual Site Model Guidance
ASTM standard guidance document E1689-95 (ASTM 2014) "Standard Guide for Developing
Conceptual Site Models for Contaminated Sites" (ASTM 2014)" was used as a general
component of this CSA. The guidance document provides direction in developing conceptual
site models used for the integration of technical information from multiple sources, selection of
sampling locations to establish background concentrations of substances, identification of data
needs and guidance of data collection activities, and evaluation of risks to human and
environmental health posed by a contaminated site. According to ASTM E1689-95, six basic
activities are associated with developing a conceptual site model:
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1.0 INTRODUCTION
• Identification of potential contaminants;
• Identification and characterization of the source(s) of contaminants;
• Delineation of potential migration pathways through environmental media, such as
groundwater, surface water, soils, sediment, biota, and air;
• Establishment of background areas of contaminants for each contaminated medium;
• Identification and characterization of potential environmental receptors (human and
ecological); and
• Determination of the limits of the study area or system boundaries.
Development of a conceptual site model is typically iterative and the complexity of the model
should be consistent with the complexity of the site and available data. Information gained
through site investigation activities is used to characterize existing physical, biological, and
chemical systems at a site. The conceptual site model describes and integrates processes that
determine contaminant releases, contaminant migration, and environmental receptor exposure
to contaminants. Development of the model is essential to determine potential exposure routes
and identifying possible impacts to human health and the environment (ASTM 2014).
The conceptual site model is used to integrate site information, identify data gaps, and
determine whether additional information is needed at the site. The model is also used to
facilitate selection of remedial alternatives and effectiveness of remedial actions in reducing the
exposure of environmental receptors to contaminants (ASTM 2014).
This CSA was conducted in accordance with the conditionally approved Work Plan to meet the
NCDENR, NORR, and CAMA regulatory requirements described in Section 1.2, and using the
NORR, USEPA, and ASTM approaches described above. This assessment information will be
used to develop a CAP, to be submitted separately, for the Buck site that will provide a
demonstration of these criteria in support of the recommended site remedy.
Data obtained from sampling during this CSA are compared to federal and state regulatory
standards shown in Table 1-1. Beginning in Section 7.0, laboratory results are compared to the
above -referenced regulatory standards and discussed as either "exceeding" or "not exceeding"
those standards. The evaluation of exceedances of these standards forms the basis for
determining the need for additional work later in this document
1.5 Limitations and Assumptions
Development of this CSA is based on information provided to HDR by both public and private
entities including universities, federal, state and local governments, and information and
analytical reports generated by Duke Energy. HDR assumes the information in these
documents to be accurate and reliable. This information was used to estimate exposure routes
and migration pathways in the subsurface. This CSA was developed using a standard of care
ordinarily used by engineering practice under the same or similar circumstances, but may
include assumptions based on the accuracy and reliability of data from various entities. CAMA
Section §1 30A-309.21 1 (a) requires that "No later than 180 days from approval of the
Groundwater Assessment Plan, the owner shall submit a Groundwater Assessment Report to
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1.0 INTRODUCTION
the Department". The schedule dictated by CAMA is compressed; therefore, data interpretation
is limited and subject to change upon receipt of additional data in subsequent rounds of
sampling and additional data collected to resolve data gaps identified in Section 14.0. The
additional data will be used to inform the corrective actions identified in the CAP.
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2.0 SITE HISTORY AND DESCRIPTION
2.0 Site History and Description
This section provides a description of the Buck site based on relevant historical data and
representative information. The purpose of this characterization is to familiarize readers with the
site and use the general information as part of the overall ASTM conceptual site model
development approach.
2.1 Site Location, Acreage, and Ownership
The Buck site is located northwest of Leonard Road on the south bank of the Yadkin River near
Spencer, Rowan County, North Carolina (Figure 2-1). The Buck site occupies approximately
640 acres (Figure 2-2), and is owned by Duke Energy. As of the date of this report, site
ownership and land use prior to Duke Energy could not be determined from available records.
2.2 Site Description
Buck was a six -unit coal-fired electricity generating facility along the Yadkin River. Buck began
operation of Units 1 and 2 in 1926 as a coal-fired generating station with a capacity of 256
megawatts (MW). Units 1 and 2 were retired in 1979. Units 3 and 4 at Buck, 113 MW combined,
were retired in mid-2011 and Units 5 and 6, 143 MW combined, were retired in April 2013.
There are no coal-fired units currently in operation at Buck. Construction of the 620 MW BCCS
natural gas facility began in 2008. Commercial operation of the natural gas facility began in late-
2011. Three combustion turbine units formerly operated adjacent to the coal-fired units and
were retired in October 2012. Buildings and other structures associated with power production
are generally located in the northwestern section of the site. The eastern portion of the site is
generally wooded with the exception of the remaining ponded areas of the ash basin.
The ash basin system at Buck consists of three cells, associated earthen dikes, discharge
structures, and two canals. The cells are designated as Cell 1 Additional Primary Pond (Cell 1),
Cell 2 Primary Pond (Cell 2), and Cell 3 Secondary Pond (Cell 3). The ash basin is located to
the south (Cell 1) and southeast (Cells 2 and 3) of Buck, with a final NPDES permitted outfall
that discharges into the Yadkin River on the northeast side of Buck. A 1953 topographic map
depicting the site prior to construction of the ash basin features is provided as Figure 2-3. The
original ash basin at Buck began operation in 1957 and was formed by constructing a dam
across a tributary of the Yadkin River, and occupied the approximate combined footprint of Cells
2 and 3. The original ash basin was eventually divided into two cells (Cells 2 and 3) in 1977 by
construction of a separate divider dam and raising the western portion of the original dam. In
1982, additional storage was created by construction of Cell 1, separate from the other cells, by
building a new dam upgradient from Cell 2.
An unlined dry ash storage area is located on the eastern side of Cell 1 and contains dewatered
ash that was excavated from Cell 1 in 2009 to provide additional volume for sluiced ash. The
ash storage area is located with the footprint of and drainage area of Cell 1 and has a soil cover
that is vegetated.
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2.0 SITE HISTORY AND DESCRIPTION
Topography at the Buck site ranges from an approximate high elevation of 734 feet (NAVD 88)
at the communications cell tower near the southwest edge of the property to an approximate low
elevation of 620 feet at the Yadkin River on the northern margin of the site, with a total elevation
change of approximately 114 feet over an approximate distance of 0.9 miles. Surface water
drainage flow generally follows site topography from the south to north across the site except
where natural drainage patterns have been modified by the ash basin or other construction
features (refer to Section 3.2). A site features map is shown in Figure 2-4.
2.3 Adjacent Property, Zoning, and Surrounding Land Uses
Properties located within a 0.5-mile radius of the Buck ash basin compliance boundary generally
consist of residential, agricultural, and undeveloped properties located in Rowan County to the
west, south, and east of the ash basin. The Yadkin River flows from west to east along the
northern boundary. Hunting and game lands are located north of the ash basin across the
Yadkin River in Davidson County.
Buck is zoned as Industrial (IND) by Rowan County. Properties to the east and south are zoned
Rural Agricultural (RA). Properties to the west are zoned as either Rural Agricultural with
Agricultural Overlay (RA -AO) or 1-85 Economic Development District (85-ED-2). Figure 2-5
depicts the properties surrounding Buck and zoning designations.
2.4 Adjacent Surface Water Bodies and Classifications
Surface water features located at the Buck site are shown in Figure 2-2. The site is located
within the Yadkin -Pee Dee River basin about two miles northwest of High Rock Lake. Surface
water classifications in North Carolina are promulgated in Title15A NCAC Subchapter 2B. The
Yadkin River at Buck has a classification of WS-V. Class WS-V waters are protected as water
supply sources which are generally upstream and draining to Class WS-IV waters or waters
used by industry to supply their employees with drinking water or as waters formerly used as
water supply. These waters are also protected for Class C uses which include secondary
recreation, fishing, wildlife, fish consumption, aquatic life including propagation, survival and
maintenance of biological integrity, and agriculture. Secondary recreation includes wading,
boating, and other uses involving human body contact with water where such activities take
place in an infrequent, unorganized, or incidental manner (NCDENR 2015).
Three small farm ponds are located on adjacent properties south of the Buck site. The
easternmost pond is the source of a stream that drains from south to north across the
easternmost portion of the site into the Yadkin River. The western farm ponds both drain from
south to north into the southern end of Cell 1. An unnamed stream also exists near the western
edge of the Buck site near a transmission line corridor and drains into the Yadkin River. Portions
of Cells 1, 2, and 3 of the ash basin also currently contain ponded areas of water. None of these
ponds or streams is classified.
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2.5 Meteorological Setting
In winter, the average temperature in Rowan County is 42°F and the average daily minimum
temperature is 31 °F. In summer, the average temperature is 770F and the average daily
maximum temperature is 89°F (USDA-NRCS 2004). The total average annual precipitation in
Rowan County is 46 inches. Thunderstorms occur approximately 41 days each year (USDA-
NRCS 2004). The average relative humidity in midafternoon is approximately 54 percent, with
humidity reaching higher levels at night. The prevailing wind is from the southwest, and average
wind speed is highest (8.8 miles per hour) in March and April (USDA-NRCS 2004).
2.6 Hydrologic Setting
The general direction of groundwater flow can be approximated from the ground surface
topography with groundwater discharge to streams and the Yadkin River, and from groundwater
elevation measurements. Two unnamed tributaries of the Yadkin River are located along the
eastern and western sides of the Buck site. A topographic divide is located approximately along
Leonard Road, to the south of the ash basin. The topographic divide likely also functions as a
groundwater hydrologic boundary. The Yadkin River is located to the north of Buck. The
predominant direction of groundwater flow from the ash basin is in a northerly direction,
generally towards the Yadkin River, with localized components of flow toward the unnamed
tributaries on the eastern and western sides of the site.
Water level data within Cell 1, Cell 2, and Cell 3 were reviewed from the time period between
January 1985 and March 2015. During this time period, all three cells were in operation. Cell 1
surface water levels generally exhibited gradual increases as would be expected as the level of
ash within the cell increased. Water elevations within Cell 1 remained relatively steady at
approximately 693 feet from January 1985 until April 1986 when the water elevation was raised
to 694.3 feet. The water elevations within Cell 1 remained between 694 and 695 feet until
January 2005 when the elevation was raised to 700.2 feet, and elevations thereafter remained
relatively steady between approximately 699 and 700 feet until October 2006. The water
elevations were subsequently raised to approximately 701.5 feet in October 2006, 703 feet in
January 2007, 704 feet in February 2007, and 705 feet from July 2008 through January 2009.
Water elevations varied from approximately 689 to 705 feet from January 2009 through January
2010, which included the time period when ash was being excavated out of the eastern side of
Cell 1 and into the ash storage area. Water elevations then remained relatively steady at
approximately 705 feet until dropped to approximately 700 feet in October 2013. The last coal-
fired units at Buck were retired in April 2013. Since October 2013, the water elevation within Cell
1 has remained relatively constant at approximately 701 feet through March 2015. This last drop
in water levels was initiated by Duke Energy to improve access within Cell 1 for the field
activities associated with the CSA. There have been no dam construction or modifications for
Cell 1 since before January 1985; therefore, the noted changes in water elevations were
achieved by removing and adding stop logs. Smaller variations in water elevations could be
attributed to variations in the flows from the stations and storm events.
Im
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2.0 SITE HISTORY AND DESCRIPTION
Cell 2 and Cell 3 surface water elevations have shown less variability than within Cell 1 between
January 1985 and March 2015, which is due to the use of Cell 1 as the primary means of ash
storage during this time period. Cell 2 water elevations generally fluctuated between
approximately 680 and 683 feet. Cell 3 water elevations generally fluctuated between 673 and
675 feet. These variations are likely attributed to the addition/removal of stop logs, variability in
station operations, precipitation, and /or evapotranspiration.
The ash basin affects the local groundwater elevations that underlie the ash basin. Water level
measurements recorded downgradient of the ash basin cells indicate localized groundwater
mounding due to the presence of the ash basin. Water level measurements recorded upgradient
(south) of the ash basin cells indicate that groundwater flow is to the north (toward the ash
basin).
Groundwater recharge in the area is derived entirely from infiltration of local precipitation.
Groundwater recharge occurs in areas of higher topography (i.e., hilltops) and groundwater
discharge occurs in lowland areas bordering surface water bodies, marshes, and floodplains
(LeGrand 2004). Of the average annual precipitation of 42 to 46 inches in the Piedmont area of
North Carolina, mean annual recharge ranges from 4.0 to 9.7 inches per year (Daniel 2001).
The hydrologic setting is described in greater detail in Section 5.0.
2.7 Permitted Activities and Permitted Waste
Duke Energy is authorized to discharge treated wastewater from Buck to receiving waters
designated as the Yadkin River in the Yadkin -Pee Dee River Basin in accordance with NPDES
Permit NC0004774, which was most recently renewed on January 1, 2012. Any other point
source discharge to surface waters of the state is prohibited unless it is an allowable non-
stormwater discharge or is covered by another permit, authorization, or approval.
The NPDES permit authorizes the following discharges in accordance with effluent limitations,
monitoring requirements, and other conditions set forth in the permit:
• Once -through non -contact condenser cooling water (CCW) for Buck is discharged to the
Yadkin River through Outfall 001;
• Make-up water process wastes, boiler cleaning water, stormwater flows from the yard
Buck are discharged into the ash basin and then into the Yadkin River through Outfall
002;
• Discharges from the BCCS wastewater collection sump (yard and floor drains from the
generation equipment areas and auxiliary systems, water treatment building area, fire
protection system, sanitary waste system, condenser circulating system, cooling tower
blow down) are discharged into the ash basin and then into the Yadkin River through
Outfall 002;
• Yard sump overflow from Buck is discharged into the Yadkin River through Outfall 002A;
• Outfall 003 has been eliminated;
• Intake screen backwash from Buck is discharged into the Yadkin River through Outfall
004; and
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2.0 SITE HISTORY AND DESCRIPTION
• Miscellaneous equipment cooling water from Buck is discharged into the Yadkin River
through Outfall 005.
Most of the discharges listed above as associated with Buck have been reduced or eliminated
as a result of decommissioning Buck.
There are no active or inactive permitted solid waste facilities (landfills) at the site.
NPDES and Surface Water Monitoring
The NPDES program regulates wastewater discharges to surface waters to ensure that surface
water quality standards are maintained. The NPDES permitting program requires that permits
be renewed every five years. The most recent NPDES permit renewal for Buck was issued on
January 1, 2012 and expires on August 31, 2016.
The current permit cited above requires surface water monitoring as part of the permit
conditions. Surface water samples are required to be collected associated with Outfalls 001,
002, and 002A. The sample locations, parameters, and constituents to be measured and
analyzed, and the requirements for sampling frequency and reporting results are outlined in the
permit.
2.9 NPDES Flow Diagram
The NPDES flow diagram for Buck is provided in Figure 2-6. This diagram shows the current
inflows and outflows to the ash basin. The decommissioning of Buck has significantly reduced
flows from Buck to the ash basin. Stormwater from the Buck yard drainage sump and runoff
from the basin watershed is estimated to result in an average flow of 0.364 million gallons per
day (MGD) to the basin. The estimated average sanitary waste flow from Buck to the basin is
0.002 MGD. Other remaining flows from Buck to the ash basin are relatively minor.
Current inflows into the ash basin from BCCS include approximately 1.18 MGD from the cooling
towers and condenser system, 0.040 MGD from the chiller system, and 0.073 MGD from the
plant sumps. There is also a minor flow from the BCCS septic system into the ash basin. The
contributing sources to these inflows are depicted on Figure 2-6.
Figure 2-6 indicates a total outflow of 4.4 MGD from the ash basin, which includes ash sluice
and other flows that are no longer directed to the ash basin since the decommissioning of the
Buck. Based on the current outflows described above, the current discharge from the ash basin
is approximately 1.66 MGD.
2.10 History of Site Groundwater Monitoring
The location of the ash basin voluntary and compliance monitoring wells, the approximate ash
basin waste boundary, and the compliance boundary are shown in Figure 2-7. The compliance
boundary for groundwater quality at the Buck ash basin site is defined in accordance with Title
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2.0 SITE HISTORY AND DESCRIPTION
15A NCAC 02L .0107(a) as being established at either 500 feet from the waste boundary or at
the property boundary, whichever is closer to the waste.
2.10.1 Voluntary Groundwater Monitoring Wells
Monitoring wells MW-1 S, MW-1 D, MW-2S, MW-2D, MW-3S, MW-3D, MW-4S, MW-4D, MW-5S,
MW-5D, MW-6S, and MW-6D were installed by Duke Energy in 2006 as part of the voluntary
monitoring system for groundwater near the ash basin. The existing voluntary wells are shown
on Figure 2-7. Duke Energy performed biannual voluntary groundwater monitoring around the
Buck ash basin from November 2006 until May 2010. During this period, twelve voluntary
groundwater monitoring wells were sampled biannually and the analytical results were
submitted to NCDENR DWR.
Voluntary monitoring wells MW-2S and MW-2D were abandoned during construction of BCCS.
With the exception of MW-6S, MW-6D, MW-3S, and MW-3D, no samples are currently being
collected from the voluntary wells and they are not included in this CSA.
2.10.2 Compliance Groundwater Monitoring Wells
Compliance groundwater monitoring, as required by the Buck NPDES Permit NC0004774,
includes 14 compliance wells and began in March 2011. NPDES Permit Condition A (11),
Version 1.1, dated June 15, 2011, lists the groundwater monitoring wells to be sampled, the
parameters and constituents to be measured and analyzed, and the requirements for sampling
frequency and reporting results (provided in Table 2-1). Locations for the compliance
groundwater monitoring wells were approved by the former NCDENR DWR Aquifer Protection
Section.
The compliance groundwater monitoring system for the Buck ash basin consists of the following
monitoring wells: MW-6S, MW-6D, MW-7S, MW-7D, MW-8S, MW-8D, MW-9S, MW-9D, MW-
10D, MW-11 S, MW-11 D, MW-12S, MW-12D, and MW-13D. Compliance groundwater
monitoring wells were installed in December 2010. All compliance monitoring wells are sampled
three times per year (in March, July, and November) for constituents listed in Table 2-1...
Analytical results are submitted to the NCDENR DWR before the last day of the month following
the month of sampling for all compliance monitoring wells. The compliance groundwater
monitoring is performed in addition to the current NPDES monitoring of surface water
discharges from Buck.
From March 2011 through July 2015, the compliance groundwater monitoring wells at Buck
have been sampled a total of 14 times. During this period, these monitoring wells were sampled
in:
• March, July, and November 2011
• March, July, and November 2012
• March, July, and November 2013
• March, July, and November 2014
• March and July 2015
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One or more 2L Standards have been exceeded in groundwater samples collected from each of
the compliance monitoring wells. Exceedances have occurred at least once in one or more wells
for boron, chromium, iron, manganese, pH, sulfate, and total dissolved solids (TDS), although
some of the analytes are naturally occurring in the regional geology. Table 2-2 presents
exceedances measured from March 2011 through March 2015.
Monitoring wells MW-6S, MW-7S, MW-8S, MW-9S, MW-11 S, and MW-12S were installed with
10-foot to 15-foot well screens placed above auger refusal to monitor the shallow aquifer within
the saprolite layer. These wells were installed to total depths ranging from 13.8 feet below
ground surface (bgs) at MW-9S to 21 feet bgs at MW-8S.
Monitoring wells MW-6D, MW-7D, MW-8D, MW-9D, MW-1 OD, MW-11 D, MW-12D, and MW-
13D were installed with 5-foot to 15-foot well screens placed in the uppermost region of the
fractured rock transition zone. These wells were installed to total depths ranging from 29.2 feet
bgs at MW-9D to 108.5 feet bgs at MW-6D.
Monitoring wells MW-6S and MW-6D are located to the southeast of Cell 1 at the compliance
boundary and are considered to represent background water quality conditions at the site. The
other ash basin compliance monitoring wells were also installed at or near the compliance
boundary.
2.11 Assessment Activities or Previous Site Investigations
Between 1987 and 2012, several historical onsite investigations have been conducted in
response to fuel oil, diesel, and gasoline releases linked to the piping, aboveground storage
tanks (ASTs), and underground storage tanks (USTs) associated with operations at Buck. A
summary of the historical environmental incidents on -site is provided in Table 2-3.
In September 2013, Duke Energy commenced implementation of a geotechnical and
environmental field exploration program at Buck in support of development of a conceptual
closure plan for the ash basin and ash storage area. The work performed as part of this effort
included the installation of 29 borings in and around the Buck ash basin. Monitoring wells were
installed within ash, soil, and bedrock for the purpose of environmental sampling and to
measure groundwater elevations at the site. Samples of ash pore water, groundwater, ash, soil,
and surface water were analyzed. Geotechnical testing was also performed on samples of ash
and soil. The results from this field exploration and testing program were summarized in a
conceptual design data report for the Buck ash basin closure (HDR 2014c). Pertinent
information contained within the data report is included within this CSA report to supplement
data obtained from the recent field activities.
2.12 Decommissioning Status
Initial decommissioning activities at Buck began in 2013 and involved relocation of remaining
coal by truck, relocation of plant equipment, removal of combustion turbine units and coal
handling equipment, asbestos removal, and modifications to select gas plant systems. Ongoing
decommissioning activities include relocation of electrical equipment and demolition of auxiliary
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2.0 SITE HISTORY AND DESCRIPTION
buildings and structures (scheduled to be completed by the end of 2015), removal of remaining
powerhouse equipment and material for salvage and demolition of powerhouse and chimneys
(scheduled to begin in 2016), and restoration of the Buck (scheduled to begin in 2017).
In conjunction with decommissioning activities and in accordance with CAMA requirements,
Duke Energy will permanently close the Buck ash basin. The required date of closure depends
on the risk ranking classification assigned to the basin by NCDENR. DENR is required to submit
their recommended risk ranking classification to the Coal Ash Commission no later than
December 31, 2015.
Classification of the Buck ash basin as a high -risk impoundment would require the basin to be
excavated and closed as soon as practical, but no later than December 31, 2019, and a
proposed closure plan must be submitted to NCDENR no later than December 31, 2016. A
high -risk classification would require the basin to be excavated and closed by either converting
the impoundment to a lined industrial landfill or by removal of all CCR from Buck and placement
within an off -site landfill, structural fill, or other beneficial use allowed by law.
Classification of the Buck ash basin as an intermediate -risk impoundment would require the
basin to be excavated and closed as soon as practical, but no later than December 31, 2024. A
proposed closure plan for such a classification must be submitted to NCDENR as soon as
practical, but no later than December 31, 2017. An intermediate -risk classification would require
the basin to be excavated and closed by one of the same options listed for high -risk
impoundments.
Classification of the Buck ash basin as a low -risk impoundment would require the basin to be
closed as soon as practical, but no later than December 31, 2029. A proposed closure plan for
such a classification must be submitted to NCDENR as soon as practical, but no later than
December 31, 2018. A low -risk classification would allow the basin to be closed by one of the
same options listed for high -risk impoundments but will also allow closure in -place by
construction of a cap system over the CCR designed to minimize infiltration and erosion. The
final USEPA CCR rule (U.S. Environmental Protection Agency 2015), however, requires
breaching of the impoundment dike and stabilization of the ash within the impoundment if
saturated ash is present within the impoundment.
Per the requirements of the USEPA CCR Rule, Duke Energy is preparing a Closure Plan that
will be required to be posted on an external website by October 2016. The insights gained from
this CSA and the associated CAP will inform the closure plan development.
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3.0 SOURCE CHARACTERISTICS
3.0 Source Characteristics
This section provides a general description of the Buck coal combustion and ash handling
system, a description of the ash basin and ash storage area, and provides a discussion on the
general physical and chemical properties of ash.
3.1 Coal Combustion and Ash Handling System
Coal ash is produced from the combustion of coal. The coal is dried, pulverized, and conveyed
to the burner area of a boiler. The smaller particles produced by coal combustion, referred to as
fly ash, are carried upward in the flue gas and are captured by an air pollution control device,
such as an electrostatic precipitator. The larger particles of ash that fall to the bottom of the
boiler are referred to as bottom ash.
Coal ash residue from the coal combustion process was disposed in the Buck ash basin from
approximately 1957 until the last coal-fired generating units were retired in April 2013. Fly ash
from the electrostatic precipitators was collected in hoppers. Bottom ash and boiler slag was
collected in the bottom of the boilers. After collection, both fly ash and bottom ash/boiler slag
were sluiced to the ash basin using conveyance water withdrawn from the Yadkin River. The
sluice lines originally discharged the water/ash slurry and other flows into the northwest section
of Cell 2. After Cell 1 was constructed in 1982, the discharge lines from Buck were redirected
into the northeast section of Cell 1. Refer to Figure 2-2 for a depiction of these features.
During operation of the coal-fired units, the ash basin received variable inflows from the ash
removal system and other permitted discharges. Currently, the ash basin receives variable
inflows from the Buck station yard drain sump, stormwater flows, and miscellaneous low volume
wastes. The basin also receives variable inflows from the BCCS wastewater collection sump.
Duke Energy is in the process of evaluating alternatives for removing these flows from the ash
basin to allow total decommissioning of the ash basin system.
3.2 Description of Ash Basins and Ash Storage Area
The Buck ash basin system is located near the Yadkin River and comprises three cells
designated as Cell 1, Cell 2, and Cell 3 (as previously described in Section 2.2), and associated
embankments and outlet works, as shown in Figure 2-2. The ash basin is located to the south
(Cell 1) and southeast (Cells 2 and 3) of the retired Buck Units 1 through 6 and the BCCS. An
area between Cell 1 and Cell 2 has also been utilized for storage of dredged ash from Cell 1
and is referred to as the ash storage area. Buck historically produced approximately 100,000
tons of ash per year. Note that this quantity is an estimate and actual quantities fluctuated
based on generation rates, outages, coal mineralogy, and other factors. The ash basin system
will sometimes be referred to collectively as the ash basin or source for convenience in this
report.
Beyond Cell 1, Cell 2, Cell 3 and the ash storage area adjacent to Cell 1, no other CCR waste
storage or disposal areas are known to exist at the Buck site.
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3.0 SOURCE CHARACTERISTICS
3.2.1 Ash Basin
The original ash basin at Buck began operation in 1957 and was formed by constructing a dam
across a tributary of the Yadkin River with a crest elevation of 680 feet. The footprint of the
original ash basin was the approximate current footprint of Cells 2 and 3. As the ash basin
capacity diminished over time, the original basin was eventually divided into two ash basins
(Cells 2 and 3) by construction of a separate intermediate dike over ash and raising the
elevation of the western portion of the earthen dike along the Yadkin River by 10 feet in 1977.
In 1982, additional storage was created by construction of Cell 1, separate and upgradient from
Cell 2, by building a new dike with a crest elevation of 710 feet. Until Cell 1 was constructed,
ash generated from the coal combustion process at Buck was sluiced (via ash discharge lines)
into the northwest section of Cell 2. Following construction of Cell 1, discharge of sluiced ash
into the ash basin system was rerouted from Cell 2 to the northeast section of Cell 1.
All coal ash from Buck was disposed of in the ash basin from approximately 1957 until 2013. Fly
ash precipitated from flue gas and bottom ash collected in the bottom of the boilers were sluiced
to the ash basin using conveyance water withdrawn from the Yadkin River.
The discharge flow from Cell 1 enters Cell 2 via the Cell 1 discharge tower. Flow from Cell 2
enters Cell 3 via the Cell 2 discharge tower. Flow is discharged through NPDES Outfall 002 to
the Yadkin River through the Cell 3 discharge tower located at the north end of Cell 3. The Cell
3 concrete discharge tower drains through a 36-inch-diameter corrugated metal pipe.
The approximate current basin elevations (obtained June 2015) for the three ash basin cells
are: Cell 1 — pond elevation 701 feet; Cell 2 — pond elevation 682 feet; Cell 3 — pond elevation
673 feet. The elevation of the Yadkin River near the site is approximately 620 feet. The ash
basin pond elevations are controlled by the use of concrete stop logs in the three discharge
towers.
The area contained within the waste boundary for Cell 1 encompasses approximately 90 acres.
For purposes of delineating the waste boundary, Cells 2 and 3 are considered a single unit, with
the area contained within this portion of the waste boundary encompassing approximately 80.7
acres. The ash basin waste boundary is shown on Figure 2-2.
The quantity of ash contained within the ash basin was estimated by comparing the digitized
pre -basin topographic survey of the site to a topographic and bathymetric survey of the basin,
dated November 2013, which was after the last coal-fired generating unit was retired. The
estimated in -place quantities of ash are: Cell 1 — 2,366,000 cubic yards (cy), Cell 2 — 1,624,000
cy, and Cell 3 — 227,000 cy. Actual ash quantities may vary from those calculated since soil
borrow operations are known to have taken place within the ash basin boundaries prior to the
deposition of ash.
During operation of the coal-fired units, the ash basin received variable inflows from the ash
removal system and other permitted discharges. Currently, the ash basin receives variable
inflows from the station yard drain sump, stormwater flows, and BCCS wastewater and no
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3.0 SOURCE CHARACTERISTICS
longer receives sluiced ash. Duke Energy is evaluating alternatives for removing these flows
from the ash basin in order to allow total decommissioning of the ash basin system.
Cell 3 and the southern portion of Cell 2 continue to serve as treatment units for the ash basin
system. Trees and other vegetation have naturally established in the northern portion of Cell 2.
The water level within Cell 1 has been lowered such that there is relatively little ponding
occurring within the cell.
3.2.2 Ash Storage Area
An unlined ash storage area is located topographically upgradient and adjacent to the east side
of Cell 1 (Figure 2-2). The dry ash storage area was constructed in 2009 by excavating ash
within the eastern half of Cell 1 in order to provide additional capacity for sluiced ash and covers
approximately 14 acres. Following the completion of excavation and stockpiling, the dry ash
storage area was graded to drain to Cell 1 and a minimum of 18 and 24 inches of soil cover
were placed on the top slopes and sideslopes, respectively, and vegetation was established.
The estimated in -place quantity of ash stored at this location is 209,000 cy based on a
comparison of original site topography and the topographic survey of the site from November
2013.
3.2.3 Dams
There are five regulated earthen dams within the Buck ash basin system. These include the Cell
2/Cell 3 main dam located adjacent to the Yadkin River, the Cell 1 dam located south of the
BCCS, an intermediate dam that divides Cell 2 and Cell 3, and the small dams associated with
the Cell1 and Cell 2 discharge towers.
The Cell 2/Cell 3 main dam was constructed in 1956 and was formed by constructing a dam
across a tributary of the Yadkin River with a crest elevation of 680 feet and a total height at its
deepest point of approximately 60 feet. As the ash basin capacity diminished over time, the
original basin was eventually divided into two cells (Cells 2 and 3) by construction of a separate
intermediate dike over ash and raising the elevation of the western portion of the earthen dike
along the Yadkin River by 10 feet (in 1977). At this same time, the canal for the Cell 2 discharge
tower was excavated and the dam associated with the discharge tower was constructed with a
base elevation at 670 feet and a crest elevation of 690 feet. In 1979, the intermediate dam
dividing Cell 2 and Cell 3 was reinforced by constructing an earthen embankment with a crest
elevation of 682 feet over ash on the downstream side of the dam. The embankment has a
washed stone blanket drain between the soil and underlying ash.
In 1982, additional storage was created by construction of Cell 1 with a crest elevation of 710
feet and a total height at its deepest point of approximately 60 feet. At this same time, the canal
for the Cell 1 discharge tower was excavated and the dam associated with the discharge tower
was constructed with a base elevation at 685 feet and a crest elevation of 710 feet.
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3.3 Physical Properties of Ash
Ash in the Buck ash basin consists of fly ash and bottom ash produced from the combustion of
coal. The physical and chemical properties of coal ash are determined by reactions that occur
during the combustion of the coal and subsequent cooling of the flue gas. In general, coal is
dried, pulverized, and conveyed to the burner area of a boiler for combustion. As described in
Section 3.1, material that forms larger particles of ash and falls to the bottom of the boiler is
referred to as bottom ash. Smaller particles of ash, known as fly ash, are carried upward in the
flue gas and are captured by an air pollution control device
Approximately 70 to 80 percent of the ash produced during coal combustion is fly ash (EPRI
1993). Typically 65 to 90 percent of fly ash has particle sizes that are less than 0.010 millimeter
(mm). In general, fly ash has a grain size distribution similar to that of silt. The remaining 20 to
30 percent of ash produced is considered to be bottom ash. Bottom ash consists of angular
particles with a porous surface and is normally gray to black in color. Bottom ash particle
diameters can vary from approximately 0.05 to 38 millimeters. In general, bottom ash has a
grain size distribution similar to that of fine to medium sand (EPRI 1995).
Based on published literature not specific to this site, the specific gravity of fly ash typically
ranges from 2.1 to 2.9 and the specific gravity of bottom ash typically ranges from 2.3 to 3.0.
The permeability of fly ash and bottom ash vary based on material density, but would be within
the range of sand -gravel with a similar gradation and density (EPRI 1995). Permeability and
other physical properties of the ash found in the Buck ash basin are presented later in this
report.
3.4 Chemical Properties of Ash
In general, the specific mineralogy of coal ash varies based on many factors including the
chemical composition of the coal, which is directly related to the geographic region where the
coal was mined, the type of boiler where the combustion occurs (i.e., thermodynamics of the
boiler), and air pollution control technologies employed.
The overall chemical composition of coal ash resembles that of siliceous rocks from which it
was derived, particularly shale. Oxides of silicon, aluminum, iron, and calcium make up more
than 90 percent of most siliceous rocks, soils, fly ash, and bottom ash. Other major and minor
elements (sulfur, sodium, potassium, magnesium, titanium) make up an additional 8 percent,
while trace constituents account for less than 1 percent. The following constituents are
considered to be trace elements: arsenic, barium, cadmium, chromium, lead, mercury,
selenium, copper, manganese, nickel, lead, vanadium, and zinc (EPRI 2010).
According to Duke Energy, the specific coal sources used at Buck were low sulfur coal from
central Appalachia, comprised of eastern Kentucky, southern West Virginia, and southwestern
Virginia.
The majority of fly ash particles are glassy spheres mainly composed of amorphous or glassy
aluminosilicates, crystalline matter, and carbon. Figure 3-1 presents a photograph of ash
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3.0 SOURCE CHARACTERISTICS
collected from the ash basin at Duke Energy's Cliffside Steam Station, which is similar to Buck
ash. The figure shows a mix of fly ash and bottom ash at 10 pm and 20 pm magnifications. The
glassy spheres can be observed in the photograph. The glassy spheres are generally resistant
to dissolution. During the later stages of the combustion process and as the combustion gases
are cooling after exiting the boiler, molecules from the combustion process condense on the
surface of the glassy spheres. These surface condensates; however, consist of soluble salts
(e.g. calcium (Ca2+), sulfate (S042-), metals (copper (Cu), zinc (Zn), and other minor elements
(e.g. boron (B), selenium (Se), and arsenic (As)) (EPRI 1994).
The major elemental composition of fly ash (approximately 95 percent by weight) is composed
of mineral oxides of silicon, aluminum, iron, and calcium. Oxides of magnesium, potassium,
titanium and sulfur comprise approximately 4 percent by weight (EPRI 1995). Trace elemental
composition typically is approximately 1 percent by weight and may include arsenic, antimony,
barium, boron, cadmium, chromium, copper, manganese, mercury, nickel, lead, selenium,
silver, thallium, zinc, and other elements. For comparison, Figure 3-2 shows the elemental
composition of fly ash and bottom ash compared with typical values for shale and volcanic ash.
Table 3-1 shows the bulk composition of fly ash and bottom ash compared with typical values
for soil and rock. In addition to these constituents, fly ash may contain unburned carbon.
Bituminous coal ash typically yields slightly acidic to alkaline solutions with pH levels ranging
from approximately 5 to 10 on contact with water.
The geochemical factors controlling the reactions associated with leaching of ash are complex.
Factors such as the chemical speciation of the constituent, solution pH, solution -to -solid ratio,
and other factors control the chemical concentration of the resultant solution. Constituents that
are held on the glassy surfaces of fly ash such as boron, arsenic, and selenium may initially
leach more readily than other constituents. As noted in Table 3-1, aluminum, silicon, calcium,
and iron represent the larger fractions of fly ash and bottom ash by weight. The presence of
calcium may limit the release of arsenic by forming calcium -arsenic precipitates. Formation of
iron hydroxide compounds may also sequester arsenic and retard or prevent release of arsenic
to the environment. Similar processes and reactions may affect other constituents of concern;
however, certain constituents such as boron and sulfate will likely remain highly mobile.
In addition to the variability that might be seen in the mineralogical composition of the ash,
which is based on different coal types, different age of ash in the basin, and other factors, it is
anticipated that the chemical environment of the ash basin varies over time, distance, and
depth.
EPRI (2010) reports that 64 samples of coal combustion products (including fly ash, bottom ash,
and flue gas desulfurization residue) from 50 different power plants were subjected to USEPA
Method 1311 Toxicity Characteristic Leaching Procedure (TCLP) (USEPA 2008) leaching and
no TCLP result exceeded the TCLP hazardous waste limit. Figure 3-3 provides the results of
that testing. The report also presents the trace element concentrations for fly ash and bottom
ash compared to USEPA Residential Soil Screening Levels (RSLs) for ingestion and dermal
exposure. Figure 3-4 shows the 10th to 90th percentile range for trace element concentrations
(mg/kg) in fly ash and the associated USEPA RSLs. The trace element concentrations for
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3.0 SOURCE CHARACTERISTICS
arsenic were greater than the RSL for arsenic. The RSLs of the remaining constituents were
greater than or within the 10th to 90th percentile range for their trace element concentrations.
Figure 3-5 shows similar data for bottom ash. As with fly ash, the trace element concentrations
for arsenic in bottom ash were greater than the RSL for arsenic. The RSL for chromium was
within the 101h to 90th percentile range of concentrations for chromium in bottom ash. The 10th to
90th percentile range for the remaining constituents were below their respective RSLs.
Site -specific ash data is discussed in Section 7.0 of this report.
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4.0 RECEPTOR INFORMATION
4.0 Receptor Information
Section §130A-309.201(13) of the CAMA defines receptor as "any human, plant, animal, or
structure which is, or has the potential to be, affected by the release or migration of
contaminants. Any well constructed for the purpose of monitoring groundwater and contaminant
concentrations shall not be considered a receptor." In accordance with the NORR CSA
guidance, receptors cited in this section refer to public and private water supply wells (including
irrigation wells and unused wells) and surface water features. Refer to Section 12.0 for a
discussion of non -water supply wells and other receptors that were evaluated as part of this
CSA effort.
The NORR CSA receptor survey guidance requirements include listing and depicting all water
supply wells, public or private, including irrigation wells and unused wells (other than those that
have been properly abandoned in accordance with 15A NCAC 2C.0113) within a minimum of
1,500 feet of the known extent of contamination. In NCDENR's June 2015 response to Duke
Energy's proposed adjustments to the CSA guidelines, NCDENR DWR acknowledged the
difficulty with determining the known extent of contamination at this time and stated that they
expected all drinking water wells located 2,640 feet (0.5-miles) downgradient from the
established compliance boundary to be documented in the CSA reports as specified in the
CAMA requirements. The approach to the receptor survey in this CSA includes listing and
depicting all water supply wells (public or private, including irrigation wells and unused wells)
within a 0.5-mile radius of the ash basin compliance boundary.
An additional receptor survey requirement in the NORR CSA guidance is that subsurface
utilities are to be mapped within 1,500 feet of the known extent of contamination in order to
evaluate the potential for preferential pathways. Drawings of underground utilities were not
readily available for review; however, underground utilities are typically located at relatively
shallow depths below the ground surface. It is assumed that any underground utilities present at
the site would not act as potential preferential pathways for contaminant migration through
underground utility corridors to these water supply well receptors because the Yadkin River
serves as the down -gradient hydrologic divide for groundwater flow from potentially impacted
areas. Therefore, the mapping of underground features that would serve as preferential
pathways was limited to underground piping and drains located between the ash basin waste
boundaries and these surface water features.
4.1 Summary of Previous Receptor Survey Activities
Duke Energy submitted a receptor survey to NCDENR (HDR 2014a) in September 2014, and
subsequently submitted to NCDENR a supplement to the receptor survey (HDR 2014b) in
November 2014. The purpose of the receptor survey was to identify the potential exposure
locations that are critical with regard to groundwater transport modeling and human health risk
assessment. The supplementary information was obtained from responses to water supply well
survey questionnaires mailed to property owners within a 0.5-mile (2,640-foot) radius of the
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4.0 RECEPTOR INFORMATION
Buck ash basin compliance boundary requesting information on the presence of water supply
wells and well usage.
The previous survey activities included contacting and/or reviewing the following
agencies/records to identify public and private water supply sources, confirm the location of
wells, and/or identify any wellhead protection areas located within a 0.5-mile radius of the Buck
ash basin compliance boundary:
• NCDENR DWR Public Water Supply Section's (PWSS) most current Public Water
Supply Water Sources GIS point data set;
• NCDENR DWR Source Water Assessment Program (SWAP) online database for public
water supply sources;
• Environmental Data Resources (EDR) local/regional water agency records review;
• Rowan County Health Department Environmental Health Division;
• Davidson County Health Department;
• Salisbury -Rowan Utilities Department; and
• USGS National Hydrography Dataset.
In addition, a field reconnaissance was performed on March 11, 2014 to identify public and
private water supply wells (including irrigation wells and unused or abandoned wells) and
surface water features located within a 0.5-mile radius of the Buck ash basin compliance
boundary. A windshield survey was conducted from public roadways to identify water meters,
fire hydrants, valves, and any potential well heads/well houses. Duke Energy site personnel
provided information regarding water supply wells located on Duke Energy property.
During the week of October 8, 2014, 254 water supply well survey questionnaires were mailed
to property owners requesting information on the presence of water supply wells and well usage
information for each property. The mailing list was compiled from a query of the parcel
addresses included in the Rowan County GIS database utilizing the 0.5-mile offset.
Between July 30 and August18, 2015, several of the agencies/records listed above were
contacted to provide additional update information. Updated information is provided in Appendix
B.
4.2 Summary of CSA Receptor Survey Activities and Findings
As part of this CSA report, the previously completed Receptor Survey activities were updated
based on the CSA Guidelines. The update included contacting and/or reviewing the
agencies/records to identify public and private water supply sources identified in Section 4.1 and
reviewing questionnaires that were received after the submittal of the November 2014
supplement to the September 2014 receptor survey (i.e. questionnaires received after October
31, 2014).
A summary of the receptor survey findings is provided below. The identified water supply wells
are shown in the USGS receptor map in Figure 4-1 and on an aerial photograph on Figure 4-2.
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Figure 4-3 presents underground utility features near the ash basin system while Figure 4-4
presents surface water features identified on and surrounding the Buck site, Available property
and well information for the identified water supply wells is provided in Table 4-1. Table 4-2
provides names and addresses of property owners contiguous to the ash basin waste boundary
which corresponds to the parcels depicted on Figure 4-5.
• A total of 166 private water supply wells were identified within a 0.5-mile radius of the
Buck ash basin compliance boundary. The Rowan County Health Department had
records for 28 of the 166 identified private water supply wells.
• Ten additional private water supply wells are assumed at residences located within a
0.5-mile radius of the Buck ash basin compliance boundary based on the absence of
municipal water lines.
• Two public water supply wells were identified within a 0.5-mile radius of the Buck ash
basin compliance boundary. PWS 0180647 is owned by Duke Energy and resides east
of the BCCS.
• One water supply well (PWS ID: 0180647)) (including irrigation wells and unused or
abandoned wells) was identified within the Buck ash basin potential area of interest on
Duke Energy property.
• One previously identified public water supply well (PWS NC0180630) has been
determined to exist outside of the 0.5-mile radius of the Buck compliance boundary and
has been removed from Figures 4-1, 4-2, and Table 4-1. The location that was
erroneously assigned to this well (Bethel Methodist Church) was determined to no longer
be considered to have a public water supply well and therefore is now listed as a
location with a reported private water supply well (Well ID 173) on Figure 4-1, Figure 4-2,
and Table 4-1.
• One previously identified public water supply well (PWS NC0180630) was an error and
the property is now listed as having an assumed private water supply well (Well ID 176)
on Figure 4-1, Figure 4-2, and Table 4-1.
• A new house was identified within the 0.5-mile radius of the Buck ash basin compliance
boundary and is now listed as having an assumed private water supply well (Well ID
174) on Figure 4-1, Figure 4-2, and Table 4-1.
• No wellhead protection areas were identified within a 0.5-miles radius of the Buck ash
basin compliance boundary.
• Several unnamed tributaries of the Yadkin River were identified within a 0.5-mile radius
of the ash basin.
• Several surface water features that flow toward the Yadkin River were identified within a
0-5-mile radius of the Buck ash basin.
Based on the returned water supply well questionnaires since October 31, 2014, the following
revisions were noted:
• Four of the previously reported 86 "field identified" private water supply wells were
confirmed to have private water supply wells located on the properties. These wells are
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now identified as "reported" private water supply wells on Figure 4-1, Figure 4-2 and
Table 4-1. The Well IDs with revised identifications are 61,124, 152, and 166.
One new well has been identified based on information provided in the returned
questionnaires. This well is now identified as a "reported" private water supply wells on
Figure 4-1, Figure 4-2 and Table 4-1. The new Well ID is 175.
Further details of HDR's receptor survey activities and findings are presented in Appendix B
4.3 NCDENR Well Water Testing Program
Section § 130A-309.211 (c) of the CAMA requires the owner of a coal combustion residuals
surface impoundment to conduct a Drinking Water Supply Well Survey that identifies all drinking
water supply wells within 0.5-mile down -gradient from the established compliance boundary of
the impoundment and submit the Well Survey to NCDENR. Since the direction of groundwater
flow was not fully established at the site, NCDENR required the sampling to include all potential
drinking water receptors within 0.5-mile of the compliance boundary in all directions. Between
February and July 2015, NCDENR arranged for independent analytical laboratories to collect
and analyze water samples obtained from private wells identified during the Well Survey, if the
owner agreed to have their well sampled.
Appendix B provides tabulated sampling results provided by Duke Energy from NCDENR, a
water supply well tracking spreadsheet provided by NCDENR, and well sample results provided
by NCDENR for wells outside of the 0.5-mile radius that would be considered to represent
background results.
For many of the wells sampled in this program, as with standard practice, samples were split for
analysis by Duke Energy's certified (North Carolina Laboratory Certification #248) laboratory.
The results were judged by Duke Energy to be substantially the same as the NCDENR results
and have been excluded.
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5.0 Regional Geology and Hydrogeology
5.1 Regional Geology
North Carolina is divided into three physiographic provinces: the Atlantic Coastal Plain,
Piedmont, and Blue Ridge (Fenneman 1938). The Buck site is located in in the Piedmont
Province. The Piedmont province is bounded to the east and southeast by the Atlantic Coastal
Plain and to the west by the escarpment of the Blue Ridge Mountains, with a width of 150 to 225
miles in the Carolinas (LeGrand 2004).
The topography of the Piedmont region is characterized by low, rounded hills and long, rolling,
northeast -southwest trending ridges (Heath 1984). Stream valley to ridge relief in most areas
ranges from 75 to 200 feet. Along the Coastal Plain boundary, the Piedmont region rises from
an elevation of 300 feet above mean sea level, to the base of the Blue Ridge Mountains at an
elevation of 1,500 feet (LeGrand 2004).
The Buck site is within the Charlotte terrane, one of a number of tectonostratigraphic terranes
that have been defined in the southern and central Appalachians and is in the western portion of
the larger Carolina superterrane (Figure 5-1; Horton et al. 1989; Hibbard et al. 2002; Hatcher et
al. 2007). On the northwest side, the Charlotte terrane is in contact with the Inner Piedmont
zone along the Central Piedmont suture along its northwest boundary and is distinguished from
the Carolina terrane to the southeast by its higher metamorphic grade and portions of the
boundary may be tectonic (Secor et al. 1998; Dennis et al. 2000).
The Charlotte terrane is dominated by a complex sequence of plutonic rocks that intrude a suite
of metaigneous rocks (amphibolite metamorphic grade) including mafic gneisses, amphibolites,
metagabbros, and metavolcanic rocks with lesser amounts of granitic gneiss and ultramafic
rocks with minor metasedimentary rocks including phyllite, mica schist, biotite gneiss, and
quartzite with marble along its western portion (Butler and Secor 1991; Hibbard et al. 2002). The
general structure of the belt is primarily a function of plutonic contacts. A geologic map of the
area around the Buck site is shown in Figure 5-2.
The fractured bedrock is overlain by a mantle of unconsolidated material known as regolith. The
regolith includes residual soil and saprolite zones and, where present, alluvial deposits.
Saprolite, the product of chemical weathering of the underlying bedrock, is typically composed
of clay and coarser granular material and reflects the texture and structure of the rock from
which it was formed. The weathering products of granitic rocks are quartz -rich and sandy
textured. Rocks poor in quartz and rich in feldspar and ferro-magnesium minerals form a more
clayey saprolite.
5.2 Regional Hydrogeology
The groundwater system is described as being comprised of two interconnected layers, or two -
medium system: 1) residual soil/saprolite and weathered fractured rock (regolith) overlying 2)
fractured crystalline bedrock (Heath 1980; Harried and Daniel 1992; Figure 5-3). The regolith
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layer is a thoroughly weathered and structureless residual soil that occurs near the ground
surface with the degree of weathering decreasing with depth. The residual soil grades into
saprolite, a coarser grained material that retains the structure of the parent bedrock. Beneath
the saprolite, partially weathered/fractured bedrock occurs with depth until sound bedrock is
encountered. This mantle of residual soil, saprolite, and weathered/ fractured rock is a
hydrogeologic unit that covers and crosses various types of rock (LeGrand 1988). This regolith
layer serves as the uppermost zone of the unconfined groundwater system and provides an
intergranular medium through which the recharge and discharge of water from the underlying
fractured rock occurs. Within the fractured crystalline bedrock layer, the fractures control both
the hydraulic conductivity and storage capacity of the rock mass. A transition zone (TZ) at the
base of the regolith has been interpreted to be present in many areas of the Piedmont. Harned
and Daniel (1992) describe the TZ as consisting of partially weathered/fractured bedrock and
lesser amounts of saprolite that grades into bedrock and they described the zone as "being the
most permeable part of the system, even slightly more permeable than the soil zone". Harned
and Daniel (1992) suggested the TZ may serve as a conduit of rapid flow and transmission of
contaminated water.
Until recently, most of the information supporting the existence of the TZ was qualitative based
on observations made during the drilling of boreholes and water -wells, although some
quantitative data is available for the Piedmont region (Stewart 1964; Stewart et al. 1964; Nutter
and Otton 1969; Harned and Daniel 1992). Schaeffer (2009; 2014a), using a database of 669
horizontal hydraulic conductivity measurements in boreholes at six locations in the Carolina
Piedmont, statistically showed that a TZ of higher hydraulic conductivity exists in the Piedmont
groundwater system when considered within Harned and Daniel's (1992) two types of bedrock
conceptual framework.
The TZ is described as being comprised of partially weathered rock, open, steeply dipping
fractures, and low angle stress relief fractures, either singly or in various combinations below
refusal (auger, roller cone, or casing advancer; Schaeffer 2011; 2014b). The TZ has less
advanced weathering relative to the regolith and generally the weathering has not progressed to
the development of clay minerals that would decrease the permeability of secondary porosity
developed during weathering, (i.e., the new fractures developed during the weathering process,
and /or the enhancement of existing fractures). The characteristics of the TZ can vary widely
based on the interaction of rock type, degree of weathering, degree of systematic fracturing,
presence of stress -relief fracturing, and the general characteristics of the bedrock
(foliated/layered, massive, or in between). The TZ is not a continuous layer between the regolith
and bedrock; it thins and thickens within short distances and is absent in places (Schaeffer
2011; 2014b). The absence, thinning, and thickening of the TZ is related to the characteristics of
the underlying bedrock (Schaeffer 2014b).
As previously mentioned, the TZ may vary due to different rock types and associated rock
structure. Harned and Daniel (1992) further divided the bedrock into two conceptual models: 1)
foliated/layered (metasedimentary and metavolcanic sequences) and 2) massive/plutonic
(plutonic and metaplutonic complexes) structures (Figure 5-4). Strongly foliated/layered rocks
are thought to have a well -developed TZ due to the breakup and weathering along the foliation
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planes or layering, resulting in numerous rock fragments (Harned and Daniel 1992). More
massive rocks are thought to develop an indistinct TZ because they do not contain
foliation/layering and tend to weather along relatively widely spaced fractures (Harned and
Daniel 1992). Schaeffer (2014a) proved Harned and Daniel's (1992) hypothesis that
foliated/layered bedrock would have a better developed TZ than plutonic/massive bedrock. The
foliated/layered bedrock TZ has a statistically significant higher hydraulic conductivity than the
massive/plutonic bedrock TZ (Schaeffer 2014a).
LeGrand's (1988; 1989) conceptual model of the groundwater setting in the Piedmont
incorporates Daniel and Harned's (1992) above two -medium system into an entity that is useful
for the description of groundwater conditions. That entity is the surface drainage basin that
contains a perennial stream (LeGrand 1988). Each basin is similar to adjacent basins and the
conditions are generally repetitive from basin to basin. Within a basin, movement of
groundwater is generally restricted to the area extending from the drainage divides to a
perennial stream (Slope -Aquifer System; Figure 5-5; LeGrand 1988; 1989; 2004). Rarely does
groundwater move beneath a perennial stream to another more distant stream or across
drainage divides (LeGrand 1989). The crests of the water table underneath topographic
drainage divides represent natural groundwater divides within the slope -aquifer system and may
limit the area of influence of wells or contaminant plumes located within their boundaries. The
concave topographic areas between the topographic divides may be considered as flow
compartments that are open-ended down slope.
Therefore, the groundwater system is a two medium system generally restricted to the local
drainage basin. The groundwater occurs in a system composed of two interconnected layers:
residual soil/saprolite and weathered rock overlying fractured sedimentary rock. The systems
are separated by the TZ portion of the residual soil, saprolite, and weathered rock. Typically, the
residual soil/saprolite is partially saturated and the water table fluctuates within it. Water
movement is generally preferential through the weathered/fractured and fractured bedrock of
the TZ (i.e., enhanced permeability zone). The character of such aquifers results from the
combined effects of the rock type, fracture system, topography, and weathering. Topography
exerts an influence on both weathering and the opening of fractures, while the weathering of the
crystalline rock modifies both transmissive and storage characteristics.
The igneous and metamorphic bedrock in the Piedmont consist of interlocking crystals and
primary porosity is very low, generally less than 3 percent. Secondary porosity of crystalline
bedrock due to weathering and fractures ranges from 1 to 10 percent (Freeze and Cherry 1979);
but, porosity values of 1 to 3 percent are more typical (Daniel and Sharpless 1983). Daniel
(1990) reported that the porosity of the regolith ranges from 35 to 55 percent near land surface
but decreases with depth as the degree of weathering decreases.
Groundwater flow paths in the Piedmont are almost invariably restricted to the zone underlying
the topographic slope extending from a topographic divide to an adjacent stream. Under natural
conditions, the general direction of groundwater flow can be approximated from the surface
topography (LeGrand 2004).
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6.0 Site Geology and Hydrogeology
6.1 Site Geology
The Buck site and its associated ash basin system are located in the Charlotte terrane. The
Charlotte terrane consists of an igneous complex of Neoproterozoic to Paleozoic ages (Hibbard
et al. 2002) that range from felsic to mafic in composition (Butler and Secor 1999). The
Charlotte terrane is bordered on the east and southeast by the Carolina terrane and to the west
and northwest by the Inner Piedmont (Cat Square and Tugaloo terranes) and the Kings
Mountain terrane. The structural contact of the Inner Piedmont and Charlotte terrane is the
Central Piedmont Shear Zone.
The Charlotte terrane is dominated by plutonic rocks with some large areas of metavolcanic
rocks, but few metasedimentary rocks are present. The oldest rocks in the belt consist of
metamorphosed volcanic -plutonic complexes that range in composition from ultramafic to felsic
and from coarse -grained plutonic rocks through porphyritic hypabyssal rocks including extrusive
volcanic flows and tuffs. Rock types include mafic gneiss, amphibolite, metagabbro, and
metavolcanicrocks with lessor amounts of biotite gneiss, granitic gneiss, mica schist, quartzite,
and ultramafic rocks. These rocks have been intruded by a complex sequence of plutonic rocks.
The plutonic rocks are extensive and compositions include granite, diorite, monzonite, gabbro,
norite, and pyroxenite.
The Buck site is underlain by a metavolcanic complex ranging in composition from felsic to
mafic (Figure 6-1).
The installed well and sample locations are shown on Figure 6-2.
6.1.1 Soil Classification
The following soils/materials were encountered in the boreholes:
• Ash — Ash was encountered in borings advanced within the ash basin and ash storage
areas, as well as through dikes. Ash was generally described as gray to dark gray, non -
plastic, loose to medium dense, dry to wet, fine to coarse grained.
• Fill — Fill material generally consisted of re -worked silts, clays, and sands that were
borrowed from one area of the site and re -distributed to other areas. Fill was generally
classified as silty sand, clay with sand, clay, and sandy clay on the boring logs. Fill was
used in the construction of dikes, and as cover for ash storage area.
• Alluvium —Alluvium encountered in borings during the project was classified as clay and
sand with clay. In some cases alluvium was logged beneath ash.
• Residuum (Residual soils) — Residuum is the in -place weathered soil that consists
primarily of silt with sand, clayey sand, sandy clay, clay with gravel, and clayey silts.
Residuum varied in thickness and was relatively thin compared to the thickness of
saprolite.
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• Saprolite/Weathered Rock — Saprolite is soil developed by in -place weathering of rock
that retains remnant bedrock structure. Saprolite consists primarily of medium dense to
very dense silty sand, sandy silt, sand, sand with gravel, sand with clay, clay with sand,
and clay. Sand particle size ranges from fine to coarse grained. Much of the saprolite is
IHIMM-181W19
M
Geotechnical property testing was completed for disturbed and undisturbed samples in
accordance with American Society for Testing and Materials (ASTM) standards. Forty-one
undisturbed ('Shelby Tube') samples were submitted for geotechnical testing. Geotechnical
property testing for undisturbed samples comprised Unified Soil Classification System (USCS)
classification (ASTM D 2487), natural moisture content (ASTM D 2216), Atterberg Limits (ASTM
D 4318), grain size distribution, including sieve analysis and hydrometer (ASTM D 422), total
porosity calculated from Specific Gravity (ASTM D 854), and hydraulic conductivity (ASTM D
5084). Two undisturbed samples were unable to receive the full suite of index property tests due
to low recovery, wax and gravel mixed in the tube, loose material, or damaged tubes. Thirty-
three disturbed ('Split Spoon,' or'Jar') samples received grain size distribution with hydrometer
(ASTM D 422), and natural moisture content (ASTM D 2216).
The results are presented in Table 11-1.
6.1.2 Rock Lithology
The Buck site is underlain by interbedded felsic, intermediate, and mafic metavolcanic rocks.
The felsic metavolcanic rocks are fine- to medium -grained, locally coarse -grained or
agglomeritic, rhyolitic to dacitic metatuffs. The intermediate and mafic metavolcanic rocks are
fine- to medium -grained, locally coarse -grained or agglomeritic rocks of basaltic, andesitic, and
dacitic compositions. They are primarily tuffs and flows and with minor hypabyssal intrusives
present. The rocks are metamorphosed to upper amphibolite grade of metamorphism.
6.1.3 Structural Geology
The major structures in the rock are layering/foliation of the various volcanic units. The rock
ranges from non-foliation/massive to intensely foliated with steep dips. Shear zones occur along
the contacts of the volcanic units and suggesting shearing along limbs of tight isoclinal folds.
Fracture zones occur in the rock core and are generally healed with later greenschist
metamorphic minerals, primarily epidote and chlorite. Fractures and joints below refusal in the
boreholes exhibit iron and manganese staining that is indicative of water movement. The strike
orientation of the fracture zones cannot be determined from examination of the rock core but is
likely parallel to the strike of the volcanic units (northeast). Suitable rock/saprolite exposures for
determining structural orientations were not located during field reconnaissance near the site.
6.1.4 Geologic Mapping
A site visit was conducted in April 2015 to identify (and map if present) outcrops at the site and
within a 2-mile radius of the site. No rock outcrops were identified at the Buck site or within a 2-
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mile radius of the site. The geologic map presented in Figure 6-1 is based on mapping by
Goldsmith et al. (1988) with the first encountered rock type in the new boreholes shown.
6.1.5 Fracture Trace Study
6.1.5.1 Introduction
Fracture trace analysis is a remote sensing technique used to identify lineaments on
topographic maps and aerial photography that may correlate to locations of bedrock fractures
exposed at the earth's surface. Although fracture trace analysis is a useful tool for identify
potential fracture locations, and hence potential preferential pathways for infiltration and flow of
groundwater near a site, results are not definitive. Lineaments identified as part of fracture trace
analysis may or may not correspond to actual locations of fractures exposed at the surface, and
if fractures are present, it cannot be determined from fracture trace analysis whether these are
open or healed. Healed fractures intruded by diabase are common in the vicinity of the site.
Strongly linear features at the earth's surface are commonly formed by weathering along steeply
dipping to vertical fractures in bedrock. Morphological features such as narrow, sharp crested
ridges, narrow linear valleys, linear escarpments, and linear segments of streams otherwise
characterized by dendritic patterns are examples. Linear variations in vegetative cover are also
sometimes indicative of the presence of exposed fractures, though in many cases these result
from unrelated human activity or other geological considerations (e.g., change in lithology).
Straight (as opposed to curvilinear) features are commonly associated with the presence of
steeply dipping fractures. Curvilinear features in some cases are associated with exposed
moderately -dipping fractures, but these also can be a result of preferential weathering along
lithologic contacts, or along foliation planes or other geologic structure. As part of this study,
only strongly linear features were considered, as these are far more commonly indicative of
steeply dipping or vertical fractures.
The effectiveness of fracture -trace analysis in the eastern United States, including in the
Piedmont, is commonly hampered by the presence of dense vegetative cover, and oftentimes
extensive land -surface modification owing to present and past human activity. Aerial -
photography interpretation is most affected, as identification of small-scale features can be
rendered difficult or impossible in developed areas. Substantial surface alteration occurs over
an estimated 30 percent of the aerial -photography study area for the Buck site.
6.1.5.2 Methods
Available geologic maps for the area were consulted prior to performance of aerial photography
and topographic map interpretation to identify lithologies and structures in the area, and likely
fracture orientations. Low -altitude aerial photography provided by Duke Energy (from WSP
Global, Inc.) covering approximately 5 square miles, and USGS 1:24000 scale topographic
maps covering an area of approximately 38 square miles were examined.
Maps examined included portions of the Salisbury, N.C. and Southmont, N.C. USGS 7.5'
(1:24,000 scale) topographic quadrangles. Digital copies of the quadrangles were obtained and
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viewed on a monitor at up to 7x magnification. Lineaments identified were plotted directly on the
digital images. Lineaments identified from topographic map are shown and lineament trends
indicated by a rose diagram are included on Figure 6-3. Photography provided for review
included 1"=600' scale, 9 x 9 inch black -and -white (grayscale) contact prints dated April 17,
2014. Stereo coverage was complete across the area shown on Figure 6-4. The photography
was examined using a Lietz Sokkia MS-27 mirror stereoscope with magnifying binocular
eyepiece. Lineaments identified on the photographs were marked on hard copies of scanned
images (600dpi resolution), and subsequently compiled onto a photomosaic base.
Rose diagrams were prepared for lineament trends identified from both aerial -photography and
topographic -map interpretation and are included as inserts on the respective figures.
6.1.5.3 Results
Lineaments identified from topographic maps are shown, and lineament trends indicated by a
rose diagram, are included on Figure 6-3. Geologic structures, including fractures, are not well
preserved in the deeply weathered, saprolitic soil underlying the site and its immediate vicinity.
A total of 12 topographic lineaments were identified, with tends predominantly toward the north-
northeast. These occur within the metavolcanic unit and likely parallel the layering/foliation of
the metavolcanic sequence, a joint set that strikes parallel to the layering/foliation, or shear
zones (discussed in Section 6.1.3).
Lineaments identified from aerial photography are shown and lineament trends indicated by a
rose diagram are included on Figure 6-4. A total of 4 lineaments were identified, all in the form
of linear stream courses. One of these was also identified as part of topographic -maps
interpretation as noted in the preceding paragraph. Two of the lineaments trend northeast, and
the remaining two trend north-northeast.
Extensive alteration of the land surface in the study area has greatly impacted the ability to
identify small scale lineaments on aerial photography with confidence. Due to the extensive land
alterations results of aerial -photography interpretation were inconclusive. Five lineaments were
identified as shown on Figure 6-4.
6.1.6 Effects of Geologic Structure on Groundwater Flow
The most important effects of geologic structure on groundwater flow is likely along the contacts
of metavolcanic units and the fractures and shears zones noted in the rock core that are parallel
to the contacts.
6.1.7 Soil and Rock Mineralogy and Chemistry
Soil mineralogy is complete and soil chemistry analyses are incomplete as of the date of this
report. Soil and mineralogy and chemistry results through August 17, 2015 are shown in Table
6-1 (mineralogy), Table 6-2 (chemistry, % oxides), and Table 6-3 (chemistry, elemental
composition). Completed laboratory analyses of the mineralogy and chemical composition of TZ
materials are presented in Tables 6-4 (mineralogy), 6-5 (chemistry, % oxides), and 6-6
(chemistry, elemental). Rock chemistry results are complete and are presented in Table 6-7
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(chemistry, % oxides) and Table 6-8 (chemistry, elemental).The petrographic analysis of nine
rock samples (thin -sections) and the remaining soil chemistry analyses will be included in a
Buck CSA Supplement.
The dominant minerals in the soils are quartz, feldspar (both alkali and plagioclase feldspars),
kaolinite, biotite, and amphibole. Other minerals identified include mullite, vermiculite, illite, and
illite/smectites. The major oxides in the soils are Si02 (46.25% - 70.47%), A1203 (14.93% -
28.07%), and Fe203 (2.70% - 14.95%). MnO ranges from 0.02% to 0.30%. The dominant
minerals in the TZ are quartz, feldpar (both alkali and plagioclase feldspars), biotite, chlorite and
amphibolite. The major oxides in the TZ are Si02 (58.27% - 65.72%), AI203 (14.36% - 14.85%),
and Fe203 (5.87% - 9.63%). MnO ranges from 0.11 % to 0.16%. The major oxides in the rock
samples are Si02 (46.50% - 64.69%), AI203 (11.86% - 19.21 %), and Fe203 (5.62% - 11.62 %).
6.2 Site Hydrogeology
6.2.1 Groundwater Flow Direction
Based on the site investigation, the groundwater system in the natural materials (alluvium, soil,
soil/saprolite, and bedrock) at the Buck site is consistent with the regolith-fractured rock system
and is generally an unconfined, connected aquifer system without confining layers as discussed
in Section 5.2. The groundwater system at the Buck site is divided into three layers referred to in
this report as the shallow, deep (TZ), and bedrock flow layers, so as to distinguish flow layers
within the connected aquifer system.
Voluntary, compliance, and groundwater assessment monitoring wells were gauged for depth to
water and total well depth during a comprehensive groundwater elevation measurement event
on July 6 and 7, 2015. Depth to water measurements were subtracted from surveyed top of well
casing elevations to produce groundwater elevations in shallow, deep, and bedrock monitoring
wells. Groundwater flow direction was estimated by contouring these groundwater elevations.
The location of each well relative to groundwater flow from the ash basin (i.e., whether
upgradient or downgradient) is shown for the newly installed groundwater assessment wells in
Table 6-9 and for the voluntary and compliance wells in Table 6-10
In general, groundwater within the shallow wells (S), wells in the TZ (D), and wells in fractured
bedrock (BR) flow from the ash basins and toward the Yadkin River. Ground water flow for the
shallow, TZ, and fractured bedrock flow zones are shown on Figures 6-5, 6-6, and 6-7,
respectively.
6.2.2 Hydraulic Gradient
Horizontal hydraulic gradients were derived for the shallow aquifer, TZ, and fractured bedrock
wells by calculating the difference in hydraulic head over the length of the flow path between
two wells with similar well construction (e.g., both wells having 15-foot screens within the same
water —bearing unit). The following equation was used to calculate horizontal hydraulic gradient:
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1= dh / dl
where i is the hydraulic gradient; dh is the difference between two
hydraulic heads (measured in feet); and dl is the flow path length
between the two wells (measured in feet).
Applying this equation to wells installed during the CSA activities yields the following average
horizontal hydraulic gradients (measured in feet/foot):
• S and SL wells: 0.037 ft/ft
• D and BRU wells: 0.029 ft/ft
• BR wells: 0.027 ft/ft
A summary of hydraulic gradient calculations is presented in Table 6-11.
6.2.3 Effects of Geologic/Hydrogeologic Characteristics on Contaminants
Migration, retardation, and attenuation of COls in the subsurface is a factor of both physical and
chemical properties of the media in which the groundwater passes. Soil samples were collected
and analyzed for grain size, total porosity, soil sorption (Kd), and anions/cations to provide data
necessary for completion of the three-dimensional groundwater model discussed in Section
13.0. As previously agreed upon with NCDENR, the results of the groundwater model will be
presented in the CAP.
6.2.4 Site Hydrogeologic Conceptual Model
The hydrogeologic site conceptual model (SCM) is a conceptual interpretation of the processes
and characteristics of a site with respect to the groundwater flow and other hydrologic
processes at the site. The NCDENR document, "Hydrogeologic Investigation and Reporting
Policy Memorandum," dated May 31, 2007 was used as general guidance to developing the
model. General components of the SCM consist of developing and describing the following
aspects of the site: geologic/soil framework, hydrologic framework, and the hydraulic properties
of site materials. More specifically, the SCM describes how these aspects of the site affect the
groundwater flow at the site. In addition to these site aspects, the SCM:
• Describes the regional and site geology and hydrogeology (Sections 5.0, 5.1, 6.1 and
6.2);
• Presents longitudinal and transverse cross -sections showing the hydrostratigraphic
layers, (Section 8.2);
• Develops the hydrostratigraphic layer properties required for the groundwater model,
(Section 11.2);
• Presents a groundwater contour map showing the potentiometric surface of the shallow
aquifer, (Section 6.2.1); and
• Presents information on horizontal (Section 6.2.2) and vertical groundwater gradients
(Section 11.3).
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The SCM serves as the basis for developing and understanding the hydrogeologic
characteristics of the site and for developing a groundwater flow and transport model. Historic
site groundwater elevations and ash basin water elevations were used to develop a historic
estimated seasonal high groundwater contour map for the site. A fracture trace analysis was
also performed for the site, as well as onsite/near-site geologic mapping, to better understand
site geology and to confirm and support the SCM.
An updated SCM, based on data obtained during the CSA activities and refined through
completion of groundwater modeling, will be presented in the CAP after submittal of this CSA
report.
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7.0 Source Characterization
For purposes of this assessment the source area is defined by the ash waste boundary as
depicted on Figure 2-2. Buck sources include the ash basin system and ash storage area.
Source characterization was performed to identify the physical and chemical properties of the
ash in the source area. The source characterization involved developing selected physical
properties of ash, identifying the constituents found in ash, measuring concentrations of
constituents present in the ash porewater, and performing laboratory analyses to estimate
constituent concentrations resulting from the leaching process. The physical and chemical
properties developed as part of this characterization will be used to better understand impacts to
soil and groundwater from the source area and will also be utilized as part of the groundwater
modeling and other evaluations to be performed in the CAP.
Buck source characterization was performed through the completion of soil borings, installation
of monitoring wells, and associated solid matrix and aqueous sample collection and analysis.
Ash samples were collected for analysis of physical characteristics (e.g., grain size, porosity,
etc.) to provide data for evaluation of retention/transport properties within and beneath the ash
basin and ash storage area. Ash samples were collected for analysis of chemical characteristics
(e.g., total inorganics, leaching potential, etc.) to provide data for evaluation of constituent
concentrations and distribution. Samples were collected in general accordance with the Work
Plan. Source characterization procedures and variances are documented in Appendix C. Field
parameters are documented in Appendix H.
For the purpose of this section of the report, COls are any constituents that exceeded their
applicable regulatory standard in the ash, ash basin surface water, and ash porewater. Sample
results were compared to the following regulatory standards or criteria for the purpose of
identifying COIs:
• Ash — NCDENR DWM IHSB Preliminary Industrial Health and/or Protection of
Groundwater PSRGs'
• Ash basin surface water — 2B Standards
• Ash basin porewater — 2L Standard or IMAC
These comparisons are useful in understanding potential impacts to soil, groundwater, and
surface water. However, the exceedances of standards or criteria identified in this comparison
do not necessarily indicate that exceedances of groundwater, surface water, or soil standards
are present outside the ash basin. For example, comparison of analytical results for ash
samples to cleanup standards for soil can provide insight to the types of constituents and the
concentrations present in ash relative to those standards; however, an exceedance of a PSRG
value in an ash sample does not necessarily indicate that exceedances are present in the
underlying soil.
North Carolina Department of Environment and Natural Resources Division of Waste Management
Inactive Hazardous Sites Branch Preliminary Soil Remediation Goals March 2015.
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Ash, ash basin surface water, ash porewater, and seep sample locations used for source
characterization are shown on Figure 7-1. Ash porewater refers to water samples collected from
wells installed within the ash basin and ash storage area and screened in the ash layer and
although compared to 2L Standards, porewater is not considered to be groundwater. A
summary of constituents and laboratory methods used for analysis of solid matrix samples (soil
and ash) are presented in Table 7-1. Laboratory results of total inorganic and anion/cation
analyses of ash samples collected from the ash basins and ash storage area are presented in
Table 7-2.
Laboratory parameters and analytical methods for aqueous matrix (i.e., ash basin surface water,
porewater, and seeps) are presented in Table 7-3. Laboratory results of ash basin surface water
samples are presented in Table 7-4. Ash basin porewater sample results are presented in Table
7-5. Synthetic Potential Leaching Procedure (SPLP) analyses of ash samples are presented in
Table 7-6.
As described in the approved Work Plan, both unfiltered and filtered (0.45 um filter) porewater,
surface water, and seep samples were collected for analyses of constituents whose results may
be biased by the presence of turbidity.2 Unless otherwise noted, concentration results discussed
are for the unfiltered samples and represent total concentrations.
7.1 Ash Basin
7.1.1 Ash (Sampling and Chemical Characteristics)
Twenty borings (AB-1 D, AB-2S/SL/D/BR, AB-3S/D, AB-4S/SL/BRU/BR, AB-5S/SL/BRU, AB-
6BRU, AB-7S/SL/BRU, and AB-8S/D) were advanced within the ash basin waste boundary to
obtain ash samples for chemical analyses. Most of the ash samples were obtained from Deep
(D) or Upper Bedrock (BRU) borings, although some samples were obtained from the other
borings when there were recovery issues.
Eight COls were reported above the North Carolina PSRGs for Industrial Health and/or
Protection of Groundwater Standards within the ash basin waste boundary: arsenic, barium,
boron, cobalt, iron, manganese, selenium, and vanadium (see Table 7-2).
Arsenic exceeded its Industrial Health and Protection of Groundwater PSRGs in all but one of
the ash basin ash samples, and the single non-exceedance was below a detection level greater
than both PSRGs. Iron and vanadium exceeded their respective Protection of Groundwater
PSRGs in all of the ash basin ash samples but did not exceed any of their Industrial Health
PSRGs. With the exception of four samples that were below a detection level greater than the
Protection of Groundwater PSRG, cobalt exceeded its Protection of Groundwater PSRG in all of
the ash basin ash samples but did not exceed its Industrial Health PSRG in any of those
samples. Manganese exceeded its Protection of Groundwater PSRG in roughly half of the ash
samples collected but did not exceed its Industrial Health PSRG in any of the samples.
2 The USEPA (EPA 2002) recommends that when possible, especially when sampling for contaminants
that may be biased by the presence of turbidity, the turbidity reading is desired to stabilize at a value
below 10 Nephelometric Turbidity Units (NTUs)
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Selenium exceeded its Protection of Groundwater PSRG in roughly one quarter of ash basin
ash samples but did not exceed its Industrial Health PSRG in any of the samples. Note that all
of the selenium exceedances were estimated below laboratory reporting limits. Boron only
slightly exceeded its Protection of Groundwater PSRG in one sample from AB-6BRU but did not
exceed its Industrial Health PSRG in that sample. Barium only exceeded its Protection of
Groundwater PSRG in two samples from AB-2D and AB-7BRU but did not exceed its Industrial
Health PSRG in those samples. All other constituents were less their applicable PSRGs for all
ash basin ash samples analyzed.
7.1.2 Ash Basin Surface Water (Sampling and Chemical Characteristics)
Seven ash basin surface water samples (SW-AB1, SW-AB2, SW-AB3, SW-AB4, SW-AB5, SW-
A136, and SW-AB7) were collected from the surface of ponded areas within the ash basin.
Sample SW-AB1 was collected within Cell 1. Samples SW-AB2 and SW-AB3 were collected
from Cell 2. Samples SW-AB4 through SW-AB7 were collected from Cell 3.
Fourteen COIs: aluminum, antimony, arsenic, cadmium, chromium, cobalt, copper, iron, lead,
manganese, thallium, vanadium, zinc, and TDS had results exceeding 2B Standards in ash
basin surface water within the ash basin system. However, the only constituents that exceeded
2B Standards in dissolved phase samples were arsenic (at all locations except SW-AB1),
antimony (SW-AB3), and copper (SW-AB3), indicating that turbidity/suspended solids may have
influenced the totals results. All other constituents were below their respective 2B Standards in
dissolved phase samples collected at all seven ash basin surface water locations. The ash
basin water is compared to the 2B and 2L Standards or IMACs for comparative purposes and is
not considered surface water or groundwater.
7.1.3 Ash Porewater (Sampling and Chemical Characteristics)
Ash porewater refers to water samples collected from wells installed within the ash basin area
that are screened within the ash layer. HDR does not consider porewater results to be
representative of groundwater. Ten porewater monitoring wells (AB-2S/SL, AB-3S, AB-4S/SL,
AB-5S/SL, AB-7S/SL, and AB-8S) were installed within the ash basin waste boundary and
screened within the ash layer. These wells are not considered to be representative of
groundwater.
Ten COls were reported above 2L Standards or IMACs in ash porewater samples collected
from wells within the ash basin waste boundary: antimony, arsenic, barium, boron, cobalt, iron,
manganese, thallium, TDS, and vanadium. Ash porewater sample locations are shown on
Figure 7-1 and 2L Standard or IMAC exceedances are listed in Table 7-5. Exceedances of the
2L Standard or IMAC for arsenic, manganese and vanadium were observed in nearly all ash
porewater samples. Exceedances of the 2L Standard for boron were observed in roughly half of
the ash porewater samples in both totals and dissolved analyses. Exceedances of the 2L
Standard or IMAC for antimony, cobalt, and iron were observed in the majority of ash porewater
samples in totals analyses but in roughly half of ash porewater samples in the dissolved phase
(i.e., turbidity/suspended solids appear to have had an effect on certain ash porewater
samples). Exceedances of the IMAC for thallium were observed in three ash porewater samples
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(AB-2S, AB-3S, and A13-8S). An exceedance of the 2L Standard for barium was observed in a
single ash porewater sample (AB-2SL), but the dissolved phase result was less than the 2L
Standard. A single exceedance of the 2L Standard for TDS was observed in a single ash
porewater sample (AB-2S).
7.1.4 Ash Porewater Speciation
Speciation is the analysis of the composition of a particular analyte in a system. Speciation is
important for understanding the fate and transport of COIs. Ten locations, AB-2S/SL, AB-3S,
AB-4S/SL, AB-5S/SL, AB-7S/SL, and AB-8S, were sampled for chemical speciation analyses of
arsenic (III), arsenic (V), chromium (III), chromium (VI), iron (II), iron (III), manganese (ll),
manganese (IV), selenium (II), selenium (IV), and selenium (VI). Results for chemical speciation
of porewater samples are presented in Table 7-7. Further evaluation of chemical speciation
results will be included in the CAP.
7.1.5 Radiological Laboratory Testing
Dissolved radionuclides from naturally occurring sources (e.g. soil or rock) may exist in water.
The USEPA regulates various radionuclides in drinking water. For purposes of this assessment,
radium-226, radium-228, uranium-233, uranium-234, uranium-236, and uranium-238 were
analyzed. Three locations, BG-1 D, BG-1 S, and MW-3D were sampled for the analytes listed
above. Results for radiological laboratory testing of porewater samples are presented in Table
7-8. Further evaluation of radiological laboratory testing results will be included in the CAP.
7.2 Ash Storage Area
7.2.1 Ash (Sampling and Chemical Characteristics)
Five borings (AS-1 S/D, AS-2D, and AS-3S/D) were advanced within the ash storage area waste
boundary to obtain ash samples for chemical analyses.
Six COls were reported above the North Carolina PSRGs for Industrial Health and/or Protection
of Groundwater Standards within the ash storage area waste boundary: arsenic, cobalt, iron,
manganese, selenium, and vanadium (see Table 7-2). Arsenic exceeded its Industrial Health
and Protection of Groundwater PSRGs in all of the ash basin ash samples collected. Cobalt,
iron and vanadium exceeded their respective Protection of Groundwater PSRGs in all of the ash
basin ash samples but did not exceed any of their Industrial Health PSRGs. Manganese
exceeded its Protection of Groundwater PSRG in the majority of the ash samples collected but
did not exceed its Industrial Health PSRG in any of the samples. Selenium exceeded its
Protection of Groundwater PSRG in only one of the six ash samples analyzed from the ash
storage area but did not exceed its Industrial Health PSRG in that sample. All other constituents
were less than their applicable PSRGs for all ash storage area samples analyzed.
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7.2.2 Ash Porewater (Sampling and Chemical Characteristics)
Monitoring wells installed within the ash storage area were constructed with screened intervals
set below ash since the water tables encountered at the time of drilling were below the ash/soil
interface. Thus, ash porewater within the ash storage area was not evaluated.
7.3 Seeps
7.3.1 Review of NCDENR March 2014 Sampling Results
NCDENR performed a water sampling event at Buck in March 2014. This sampling event
included only seeps. The locations and analytical results of this sampling event were provided
by NCDENR to Duke Energy and are assumed to be accurate. The location of these samples is
presented on Figure 7-1. Seep water sample identifiers and their location relative to site
features are:
• BS SWO01AA S001 (seep near Cell 3 discharge to Yadkin River)
• BS SWO03AA S001 (toe of Cell 1 dam)
• BS WWO02 S001 (Cell 3 discharge to Yadkin River)
• BSSW001 S001 (west of BCCS)
• BSSW074SO01 (east of the BSS powerhouse on bank of Yadkin River)
• BSSW076SO01(east of the BSS powerhouse on bank of Yadkin River)
Four COls exceeded their respective 2B Standards: aluminum, arsenic, selenium, and sulfate.
However, it appears that all results were for total inorganic metals and that dissolved analyses
were not performed.
March 2014 sampling results and measured field parameters were also compared to 2L
Standards and IMACs (see Table 7-9). Six COls exceeded their respective 2L standards:
arsenic, boron, iron, manganese, sulfate, and TDS.
The NCDENR seep water sample results were reviewed prior to site assessment activities and
select seep samples with exceedances of the 2B Standards and/or 2L Standards or IMAC were
identified to be re -sampled as part of the CSA assessment activities. A discussion of the seep
re -sampling results is provided below.
7.3.1.1 Resampling of NCDENR Seeps
One of the seeps was resampled in June 2015 as part of this CSA (BS WWO02 S001). The
other five seeps were dry during this sampling event and no samples were collected.
Samples collected from BS WWO02 S001 exceeded the 2L Standards or IMACs for the
following COls: antimony, arsenic, iron, manganese and vanadium (see Table 7-10).
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7.3.2 CSA Seep Sampling Results
7.3.2.1 Seeps
There are fourteen seeps (S-1 through S-10, Culvert Discharge, Wet Area Near Pump House,
Terracota Pipe #1, and Terracota Pipe #2) located within the Duke Energy property boundary
and three planned seep and surface water sampling locations (S-1A, S-1 B, and S-1 C) located
outside of the Duke Energy property boundary at Buck, excluding the previously described
NCDENR seeps. Seeps S-1 through S-4 are associated with an unnamed tributary to the
Yadkin River along the eastern property boundary and downgradient of ash basin Cell 3. Seep
S-5, Culvert Discharge, and Wet Area Near Pump House are located near the toe of Cell 2 and
Cell 3 main dam. Seep S-6 is located between ash basin Cell 2 and the Yadkin River. Seeps
Terracota Pipe #1 and Terracota Pipe #2 are located at the base of the main dam northwest of
ash basin Cell 1. Seeps S-7 through S-10 are associated with an unnamed tributary to the
Yadkin River near the western property boundary and downgradient of ash basin Cell 1. Seep
locations are shown on Figure 7-1.
Duke Energy was not able to obtain permission from the property owner to obtain off -site seep
samples S-1 A, S-1 B, and S-1 C; therefore these samples were not sampled. Seep locations Wet
Area Near Pump House and Terracota Pipe #2 were dry during the sampling event.
Of the seep locations sampled, ten COls were reported exceeding the 2L Standards or IMACs:
antimony, arsenic, boron, chromium, cobalt, iron, lead, manganese, thallium, and vanadium
(see Table 7-10). However, it is important to note that the dissolved concentrations of chromium
and iron were below their 2L Standards for all of the seep samples. Therefore, the exceedances
of these constituents in the totals phase may be due to turbidity/suspended solids. Results for
many of the seep samples indicated these same significant differences between the totals and
dissolved analyses for many constituents expected to be found above PSRGs in native soils.
The USEPA (EPA 2002) recommends that when possible, especially when sampling for
contaminants that may be biased by the presence of turbidity, the turbidity reading is desired to
stabilize at a value below 10 Nephelometric Turbidity Units (NTUs)
7.3.3 Comparison of Exceedances to 2B Standards
Samples of seep surface water obtained from around the perimeter of the ash basin exceeded
the 2B Standard for aluminum at each location with the exception of S-10. Aluminum
exceedances in the totals phase may be related to turbidity/suspended solids, as the
concentration at each location, except S-1, was below the aluminum 2B Standard in the
dissolved phase. Arsenic exceeded the 2B Standard at seep location BSWWO02 S001 only.
Cadmium exceeded the 2B Standard at seep locations S-2 and S-3. Chromium exceeded the
2B Standard at seep location S-2. Chromium exceedances in the totals phase may be related to
turbidity/suspended solids, as the concentration at each location was below the chromium 2B
Standard in the dissolved phase. Cobalt exceeded the 2B Standard at seep locations S-1, S-2,
S-3, S-5, and S-8 although the 2B Standard was only exceeded in the dissolved phase at S-1,
S-5 and S-8. Copper exceeded the 2B Standard at seep locations S-1, S-2, S-3, S-5, S-7, and
S-9. Copper exceedances in the totals phase may be related to turbidity/suspended solids, as
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the concentration at each location was below the copper 213 Standard in the dissolved phase.
Lead exceeded the 213 Standard at seep locations BSWWO02 S001, S-1, S-2, S-3, S-5, and S-
9. Lead exceedances in the totals phase may be related to turbidity/suspended solids, as the
concentration at each location was below the lead 213 Standard in the dissolved phase. Nickel
exceeded the 213 Standard at seep location S-2. Nickel exceedance in the totals phase may be
related to turbidity/suspended solids, as the concentration at this location was below the nickel
213 Standard in the dissolved phase. Zinc exceeded the 213 Standard at seep locations S-2, S-3,
and S-7. Zinc exceedances in the totals phase may be related to turbidity/suspended solids, as
the concentration at each location, except S-7, was below the zinc 213 Standard in the dissolved
phase. Constituents which exceeded the 213 Standards in the seep water samples have been
identified as seep water COIs. Sulfide was not detected in any of the seep water samples.
7.3.4 Observed Ranges of 2B Standard COI Concentrations
7.3.4.1 Background Surface Water
The background surface water location is identified as SW-2. This location was dry during the
sampling event, therefore, no observed ranges for background analytical results are available
for comparison to surface water samples from other sampling locations.
7.3.4.2 Seeps
Seep locations are identified as S-1 and S-10, Culvert Discharge, and Terracotta Pipe #1.
Ranges of totals phase concentrations for COls exceeding 213 standards are presented below.
• Aluminum
14.8 pg/L to 18,700 pg/L
• Arsenic
0.23J pg/L to 50 pg/L
• Cadmium
<0.08U pg/L to 0.21 pg/L
• Chromium
0.3J fag/L to 34.7 pg/L
• Cobalt
0.18J pg/L to 1,050 pg/L
• Copper
0.27J pg/L to 85 pg/L
• Lead
<0.1 U pg/L to 21.9 pg/L
• Nickel
0.47J pg/L to 21.8 pg/L
• Thallium
0.019J pg/L to 1.1 pg/L (single occurrence)
• Zinc
5.2J fag/L to 260 pg/L
7.3.5 Discussion of Results for Constituents without 2B Standards
Surface water samples were also analyzed for the following constituents that do not have 2B
Standards: boron, calcium, iron, manganese, mercury, selenium, and vanadium. Each of these
constituents was detected in at least one surface water sample.
7.3.5.1 Background Surface Water
The background surface water location is identified as SW-2. This location was dry during the
sampling event, therefore, no observed ranges for background analytical results for constituents
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without 2B Standards are available for comparison to surface water samples from other
sampling locations.
7.3.5.2 Seeps
Seep locations are identified as S-1 and S-10. Ranges of totals phase concentrations for Cols
without 2B Standards are presented below.
• Boron
36J fag/L and 820 fag/L
• Calcium
6,990 pg/L and 62,800 pg/L
• Iron
19.3J pg/L and 34,900 pg/L
• Manganese
3J fag/L and 6,300 pg/L
• Mercury
0.00174 pg/L and 0.87 pg/L
• Selenium
0.21 J pg/L and 10.9 pg/L
• Vanadium
1.6 pg/L and 132 pg/L
7.4 Surface Water Speciation
Speciation is the analysis of the composition of a particular analyte in a system. Speciation is
important for understanding the fate and transport of COls. Ten locations, S-1 A, S-1 B, S-1 C, BS
SW001 AA S001, BS SWO03AA S001, BS WWO02 S001, BSSW001 S001, BSSW0745001,
BSSW076S001, and BS Outfall 002 were designated to be sampled for chemical speciation
analyses of arsenic (III), arsenic (V), chromium (III), chromium (VI), iron (II), iron (III),
manganese (II), manganese (IV), selenium (II), selenium (IV), and selenium (VI). Locations S-
1 A, S-1 B, and S-1 C are associated with an off site small pond located southeast of Cell 3.
These samples could not be collected since an access agreement could not be negotiated with
the property owner. Of the remaining surface water speciation sample locations, only BS
WWO02 S001 and BS Outfall 002 could be sampled since the other locations were dry at the
time of sampling. Results for surface water speciation are presented in Table 7-11.
7.5 Leaching Potential of Ash
In addition to total inorganic testing of ash samples, 8 ash samples collected from borings
completed within the ash basin and ash storage area were analyzed for leachable inorganics
using SPLP (see Table 7-6). The purpose of the SPLP testing is to evaluate the leaching
potential, of COls that may result in impacts to groundwater above the 2L Standards or IMACs.
Although SPLP analytical results are being compared to the 2L Standards, these samples do
not represent groundwater samples. The results of the SPLP analyses indicated that the
following COI exceeded their 2L Standards or IMAC at locations shown in Figure 7-1: antimony,
arsenic, chromium, cobalt, iron, manganese, selenium, thallium, and vanadium. Leaching of
constituents from ash stored in the ash storage area will likely be different from the leaching that
occurs when ash is stored in a saturated condition, as found in the ash basins. The ash in these
two different storage environments would experience differences in the time of exposure to the
leaching solution, the liquid to solid ratio, and the chemical properties of leaching liquid. This
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would likely lead to differences in the constituents leached in the two differing environments and
in the concentrations of the leached constituents.
In general the infiltration for the ash storage area will be variable and intermittent, as infiltration
is precipitation induced. The infiltration rate is dependent on a number of factors with the
primary factors being climate, vegetation, and soil properties. The precipitation and air
temperature are the two aspects of climate that most directly affect groundwater infiltration.
Vegetation affects the infiltration rate through interception and by means of transpiration. The
primary soil properties that affect infiltration are represented by the hydraulic conductivity of the
material.
For areas where saturated conditions exist, the infiltration and subsequent groundwater
recharge would be represented by Darcy's law. However, in the case of an ash basin the
recharge flow rate calculation is complicated by the flow through the earthen dike, and through
the material underlying the ash basin (saprolite, transition zone, and bedrock). An area where
the surface is saturated or where water is present in the ash basin will receive constant
infiltration with the rate being controlled by the factors described above.
The potential migration of contaminants from the ash basin and ash storage area will occur by
the movement of ash leachate into the underlying soil layers and groundwater through
infiltration. The infiltration of precipitation for the ash storage area and the infiltration of the ash
basin water into the underlying soil material will be modeled in the groundwater model being
prepared for the CAP.
7.6 Constituents of Interest
Based on evaluation of the ash, ash basin surface water, and ash porewater sampling data, the
following COls were identified:
7.6.1 COls in Ash (based on total inorganics analysis, as shown in Table 7-2)
• Arsenic
• Barium
• Boron
• Cobalt
• Iron
• Manganese
• Selenium
• Vanadium
7.6.2 COls in Ash Basin Surface Water (based on water quality analysis (totals), as
shown in Table 7-4)
• Aluminum*
• Antimony
• Arsenic
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• Cadmium*
• Chromium*
• Cobalt*
• Copper
• Iron*
• Lead*
• Manganese*
• Thallium*
• Vanadium*
• Zinc*
• TDS
Ash basin surface water COls listed with an asterisk (*) above exhibited a significant difference
between the totals and dissolved analyses which led to the dissolved concentrations all
measured below applicable standards.
7.6.3 COls in Ash Porewater (based on water quality analysis (totals), as shown in
Table 7-5)
• Antimony
• Arsenic
• Barium*
• Boron
• Cobalt
• Iron
• Manganese
• Thallium
• TDS
• Vanadium
Ash porewater COls listed with an asterisk (*) above exhibited a significant difference between
the totals and dissolved analyses which led to the dissolved concentrations all measured below
applicable standards.
7.6.4 COls in Seeps (based on water quality analysis (totals), as shown in Table 7-10)
• Antimony
• Arsenic
• Boron
• Chromium*
• Cobalt
• Iron
• Lead*
• Manganese
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• Thallium*
• Vanadium
Ash porewater COls listed with an asterisk (*) above exhibited a significant difference between
the totals and dissolved analyses which led to the dissolved concentrations all measured below
applicable standards.
7.6.5 Summary of COIs from Source Characterization
• Antimony — exceeded relative standards in ash basin surface water, ash porewater, and
seeps.
• Aluminum — exceeded 2B Standard in apparently turbid ash basin surface water only
(i.e., no exceedances in dissolved phase)
• Antimony — exceeded relative standards in ash basin surface water, ash porewater, and
seeps
• Arsenic — exceeded relative standards in ash samples, ash basin surface water, ash
porewater, and seeps
• Barium — exceeded relative standards in ash samples and ash porewater
• Boron — exceeded relative standards in ash samples, ash porewater, and seeps
• Cadmium - exceeded 2B Standard in a single, apparently turbid ash basin surface water
only (i.e., did not exceed in dissolved phase)
• Chromium — exceeded 2B Standard in two apparently turbid seep samples (i.e., no
exceedances in dissolved phase)
• Cobalt — exceeded relative standards in ash samples, ash basin surface water, ash
porewater, and seeps
• Copper — exceeded 2B Standard in apparently turbid ash basin surface water only (i.e.,
no exceedances in dissolved phase)
• Iron — exceeded relative standards in ash samples, ash porewater, ash porewater, and
seeps
• Lead — exceeded 2B Standard in apparently turbid ash basin surface water and one
seep sample only (i.e., no exceedances in dissolved phase)
• Manganese — exceeded relative standards in ash samples, ash basin surface water, ash
porewater, and seeps.
• Selenium — exceeded relative standards in ash samples.
• TDS — exceeded relative standards in ash basin surface water and ash porewater.
• Vanadium — exceeded relative standards in ash samples, ash basin surface water, ash
porewater, and seeps.
• Zinc — exceeded 2B Standard in apparently turbid ash basin surface (i.e., no
exceedances in dissolved phase)
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8.0 SOIL AND ROCK CHARACTERIZATION
8.0 Soil and Rock Characterization
The purpose of soil and rock characterization is to characterize the soil and rock on the site for
corrective action and compare to applicable cleanup levels. Soil and rock samples were
collected and analyzed in general accordance with the procedures and methods described in
the Work Plan. Refer to Appendix D for a detailed description of these methods and variances
from the sampling plan outlined in the Work Plan, and Appendix E for field and sampling quality
control / quality assurance protocol.
Soil, PWR, and bedrock samples were collected from background locations, beneath the ash
basin ash storage area, and from locations beyond the waste boundary.
Table 8-1 summarizes the soil and rock sampling plan utilized for groundwater assessment
activities. Variances from the proposed sampling plans are presented in Appendix D. The boring
locations are shown on Figure 8-1.
8.1 Background Sample Locations
Background (BG) boring locations were identified based on the CSM at the time the Work Plan
was submitted. The BG locations (BG-1, BG-2 and BG-3) were chosen in areas assumed not to
be impacted by and topographically upgradient of the ash basin and ash storage area. Based
on the groundwater contours shown in Figures 6-5 through 6-7, and the CSM, the background
locations are considered to be hydrologically upgradient of the ash basin and ash storage area.
As a result, the BG boring locations are considered to be representative of background soil
conditions at the site.
8.2 Analytical Methods and Results
Parameters and laboratory methods used for analysis of solid matrix samples are presented in
Table 8-2. Total inorganic results for background soil samples are presented in Table 8-3. Total
inorganic results for background PWR and bedrock samples are presented in Table 8-4. Total
inorganic results for soil samples are presented in Table 8-5. Total inorganic results for PWR
and bedrock samples are presented in Table 8-6.
Figure 8-1 depicts the total inorganic results for soil, PWR, and bedrock analysis. Cross -
sections presenting the vertical distribution of COls along the transects are depicted on Figures
8-2 through 8-4.
8.3 Comparison of Soil Results to Applicable Levels
The soil analytical results are compared to the North Carolina Preliminary Soil Remediation
Goals (PSRGs) for Industrial Health and Protection of Groundwater Standards presented in
Tables 8-3 through 8-6. Frequency and concentration ranges in soil for COI exceedances of
North Carolina PSRGs are presented in Table 8-7. Frequency and concentration ranges in
PWR and bedrock for COI exceedances of North Carolina PSRGs are presented in Table 8-8.
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The subsections below provide a summary of COls that exceeded the North Carolina PSRGs in
at least one of the samples analyzed. Parameters not listed below were not reported at
concentrations exceeding the North Carolina PSRGs in the collected soil samples.
Comparison of Soil Results to Background
In addition to comparison of results to regulatory criteria, soil sample results have also been
compared to background concentrations observed in samples collected from the BG sample
locations. Boring locations are shown on Figure 8-1.
8.4.1 Background Soil
Background soil locations are identified as BG-1 D, BG-21D, and BG-3BRU. Background soil
concentration ranges are listed below for constituents that exceeded the North Carolina PSRGs
in at least one soil sampling location at the Buck site. Results with a J qualifier indicate an
estimated concentration reported between the laboratory method detection limit and the method
reporting limit. Total inorganic results for background soil samples are presented in Table 8-3.
• Arsenic
<1.7J mg/kg to <8.8U mg/kg
• Boron
46.3 mg/kg to 56.3 mg/kg
• Cobalt
7.3J mg/kg to 257 mg/kg
• Iron
18,400 mg/kg to 68,800 mg/kg
• Manganese
238 mg/kg to 3,620 mg/kg
• Selenium
4.8J mg/kg to 7.2J mg/kg
• Vanadium
70.1 mg/kg to 197 mg/kg
8.4.2 Soil Beneath Ash Basin
Soil samples within the ash basin boundary were obtained from AB-1 D, AB-21D, AB-31D, AB-
4BRU, AB-5BRU, AB-6BRU, AB-7BRU, AB-81D, AB-91D, and AB-10D/GTB. The range of
constituent concentrations in soils beneath the ash basin, along with a comparison to the range
of reported background soil concentrations, is provided in Table 8-9.
Constituent concentrations of soils beneath the ash basin tend to be generally similar to
background concentrations for all constituents. With the exception of two samples taken
beneath ash at AB-81D, barium concentrations beneath the ash basin are similar to background
concentrations.
8.4.3 Soil Beneath Ash Storage Area
Soil samples beneath the ash storage area were obtained from AS-1 D, AS-21D, and AS-3S. The
range of constituent concentrations in soil samples beneath the ash storage area, along with a
comparison to the range of reported background soil concentrations, is provided in Table 8-10.
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Constituent concentrations of soils beneath the ash storage area generally tend to be slightly
higher than background concentrations for boron and iron. Concentrations for other constituents
generally tend to be similar to background soil concentrations.
8.4.4 Soil Outside the Waste Boundary
Soil samples outside the waste boundary were obtained from GWA-1 S/D, GWA-2BRU, GWA-
3D, GWA-4D, GWA-5S/BRU, GWA-6BRU, GWA-7D, GWA-8D, GWA-9D, GWA-10D, GWA-
11 D, GWA-12S/BRU, and GWA-22D. The range of constituent concentrations in soils outside
the waste boundary, along with a comparison to the range of reported background soil
concentrations is provided in Table 8-11.
Constituent concentrations for soils outside the waste boundary tend to be similar to
background soil concentrations for all constituents.
Comparison of PWR and Bedrock Results to Background
In addition to comparison of results to regulatory criteria, PWR, and bedrock sample results
have also been compared to background concentrations as discussed below.
8.5.1 Background PWR and Bedrock
Background PWR and bedrock samples were obtained from BG-1 BR and BG-2D. Background
PWR and bedrock sample concentration ranges are listed below for constituents that exceeded
the North Carolina PSRGs in at least one PWR or bedrock sampling location at Buck. Results
with a J qualifier are estimated concentrations.
• Cobalt 6.3J mg/kg to 8.1 mg/kg
• Iron 1,170 mg/kg to 12,400 mg/kg
• Manganese 178 mg/kg to 235 mg/kg
• Vanadium 20.5 mg/kg to 43.2 mg/kg
Note that these background PWR and bedrock concentrations are based on three samples
obtained from two boring locations. It is therefore difficult to draw conclusions regarding
background conditions based on this limited data.
8.5.2 PWR and Bedrock Beneath Ash Basin
PWR and bedrock samples beneath the ash basin were obtained from AB-1 D, AB-2D/BR, AB-
3D, AB-413R. AB-5BRU, AB-6BRU, AB-7BRU, AB-8D, and AB-913R. The range of constituent
concentrations in PWR and bedrock samples beneath the ash basin, along with a comparison to
the range of reported background PWR and bedrock concentrations, are provided in Table 8-12.
Constituent concentrations for PWR and bedrock beneath the ash basin tend to be generally
similar to background soil concentrations for cobalt, iron, manganese, and vanadium.
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8.5.3 PWR and Bedrock Beneath Ash Storage Area
PWR and bedrock samples beneath the ash storage area were obtained from AS-1 D and AS-
2D. The range of constituent concentrations in PWR and bedrock samples beneath the ash
storage area, along with a comparison to the range of reported background PWR and bedrock
concentrations, is provided in Table 8-13
Constituent concentrations for PWR and bedrock beneath the ash storage area tend to be
higher than background soil concentrations for cobalt, iron, manganese, and vanadium. Note
that the maximum concentrations of arsenic, iron and manganese in PWR and bedrock beneath
the ash basin were observed in a sample obtained from 83.5 to 84.0 feet below ground surface
at AS-21D, which is well below the bottom of ash. Otherwise, arsenic, iron and manganese
concentrations were similar to background.
8.5.4 PWR and Bedrock Outside Waste Boundary
PWR and bedrock samples outside the waste boundary were obtained from GWA-31D, GWA-
5D, GWA-6D, GWA-91D, and GWA-11 D. The range of constituent concentrations in PWR and
bedrock samples outside the waste boundary, along with a comparison to the range of reported
background PWR and bedrock concentrations is provided in Table 8-14.
Constituent concentrations for PWR and bedrock outside the waste boundary tend to be higher
than background PWR and bedrock concentrations for iron, manganese, and vanadium.
Concentrations for cobalt tend to be similar to background soil concentrations.
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9.0 SEDIMENT CHARACTERIZATION
9.0 Sediment Characterization
The purpose of sediment characterization is to evaluate whether storage of ash has resulted in
impacts to surface waters in the vicinity of the ash basin and ash storage area at Buck. The
sediment characterization was performed in general accordance with the procedures described
in the Work Plan. Sampling methodology and variances from the procedures are summarized in
Appendix F. Sediment sample locations are shown on Figure 7-1.
9.1 Sediments
Sediment samples were collected coincidentally with each of the seep samples at seep
locations S-1 through S-10, BSWW002, Culvert Discharge, Terracotta Pipe #1, and Wet Area
Near Pump House. Sediment samples were analyzed for the constituent and parameter list
used for soil and rock characterization (see Table 8-2). In the absence of NCDENR sediment
criteria, the sediment sample results were compared to North Carolina PSRGs for Protection of
Groundwater and Industrial Soil. Exceedances of North Carolina PSRGs are summarized in
Table 9-1. Sediment sample locations are shown on Figure 7-1.
Seep sediment sample constituents cobalt, iron, and vanadium exceeded the North Carolina
PSRGs for Protection of Groundwater in all sediment samples but did not exceed the PSRGs
for Industrial Soil for any sample. Arsenic exceeded the PSRG for Protection of Groundwater at
sediment sample S-6 and exceeded the PSRG for Industrial Soil at sediment samples
BSWWO02 S001, S-6, Culvert Discharge, and Wet Area Near Pump House. Boron exceeded
the PSRG for Groundwater Protection at only Terracotta Pipe #1. Manganese exceeded the
PSRGs for Protection of Groundwater at each location with the exception of S-10 but did not
exceed the PSRGs for Industrial Soil at any location. Selenium exceeded the PSRG for
Groundwater Protection at only the Wet Area Near Pump House location. Antimony, cadmium,
and thallium were not detected in sediment samples collected at Buck.
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10.0 Groundwater Characterization
The purpose of groundwater characterization is to compare groundwater at the site to 2L
Standards or IMACs, and to inform the corrective actions identified in the CAP. Groundwater
sampling methods and the rationale for sampling locations were in general accordance with the
procedures described in the Work Plan. Refer to Appendix G for a detailed description of these
methods. Variances from the proposed well installation locations, methods, quantities, and well
designations are presented in Appendix G.
10.1 Regional Groundwater Data for Constituents of Interest
Individual sampling events serve to characterize the hydrogeologic and chemical conditions at a
particular monitoring location at a particular time. When interpreting the results from a sampling
event, a number of factors that affect the sample results should be taken into consideration.
Among these are the geologic and hydrogeologic setting, the location of the sample points in
the regional groundwater flow system, potential interactions between suspected contaminants
and the geological and biological constituents present in the formation (Barcelona 1985).
As a result of these factors it may be possible that the analytical results for a given constituent
are influenced by naturally occurring conditions as opposed to conditions caused by releases
from the ash basin. This section presents an overview of the regional and statewide
groundwater conditions for COls found at Buck that have promulgated state or federal
standards.
The 2L Standards recognize that the concentrations of naturally occurring substances in
groundwater may exceed the standard established in .0202(g). Rule .0202(b)(3) states that
when this occurs, the Director of the DWR will determine the standard.
North Carolina 2L Standards and IMACs are established by NCDENR, whereas primary and
secondary Maximum Contaminant Levels (MCLs and SMCLs) are established by the USEPA.
Primary MCLs are legally enforceable standards for public water supply systems set to protect
human health in drinking water. Secondary MCLs are non -enforceable guidelines set to account
for aesthetic considerations, such as taste, color, and odor (USEPA 2014).
Table 10-1 lists COls at the Buck site, along with their associated 2L Standards, IMACs, and
federal drinking water standards (MCLs and SMCLs). Regional background information on COls
at the Buck site are provided (in alphabetical order) below in Section 10.11 through 10.1.13. In
additional, regional background information on pH is also provided in Section 10.1.14 as pH
levels can affect the leachability of metal ions in groundwater.
10.1.1 Antimony
Antimony is a silvery -white, brittle metal. In nature, antimony combines with other elements to
form antimony compounds. Small amounts of antimony are naturally present in rocks, soils,
water, and underwater sediments.
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Only a few ores of antimony have been encountered in North Carolina. Antimony has been
found in combination with other metals, and is found most commonly in Cabarrus County and
other areas of the Carolina Slate Belt (Chapman 2013).
In a USGS study of naturally occurring trace minerals in North Carolina, 57 private water supply
wells were sampled to obtain trace mineral data. Of the wells sampled, no wells contained
antimony above the USEPA primary MCL (Chapman 2013). Antimony is compared to IMAC
since no 2L Standard has been established for this constituent by NCDENR.
10.1.2 Arsenic
Natural arsenic occurs commonly and comes mainly from the soil. The USEPA estimates that
the amount of natural arsenic released into the air as dust from the soil is about equal to the
amount of arsenic released by all human activities (EPRI 2008).
In a statistical summary of groundwater quality in North Carolina, the Superfund Research
Program at the University of North Carolina (UNC) analyzed private well water samples in North
Carolina. These samples were tested by the North Carolina State Laboratory of Public Health
from 1998-2010. The Buck site is located in Rowan County, North Carolina near the border of
Davidson County. Data collected from 2,341 private wells across Rowan and Davidson counties
indicated that 43 samples had arsenic concentrations exceeding the federal drinking water
primary MCL, which is the same as the 2L Standard for arsenic (NC DHHS 2010). The
summary statistics for both counties are provided in Table 10-2.
In a state-wide investigation into arsenic concentrations in private wells, Sanders et al. (2011)
found strong geological patterns in arsenic concentrations in groundwater across the state of
North Carolina (Figure 10-1). The Buck site is located in an area where concentrations of
naturally occurring arsenic in groundwater range from 1.1 - 5.0 pg/L.
10.1.3 Barium
Two forms of barium, barium sulfate and barium carbonate, are often found in nature as
underground ore deposits. Barium is sometimes found naturally in drinking water and food.
However, since certain barium compounds (barium sulfate and barium carbonate) do not mix
well with water, the amount of barium found in drinking water is typically small.
Barium compounds such as barium acetate, barium chloride, barium hydroxide, barium nitrate,
and barium sulfide dissolve more easily in water than barium sulfate and barium carbonate, but
because they are not commonly found in nature, they do not usually occur in drinking water
unless the water is contaminated by barium compounds that are released from waste sites
(EPRI 2008).
Barium is naturally released into the air by soils as they erode in wind and rain, and is released
into the soil and water by eroding rocks. Barium released into the air by human activities comes
mainly from barium mines, metal production facilities, and industrial boilers that burn coal and
oil. Anthropogenic sources of barium in soil and water include copper smelters and oil drilling
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waste disposal sites. Industries reporting to the USEPA released 119,646 tons of barium and
barium compounds into the environment in 2005 (EPRI 2008).
Regional metamorphic greenschist to upper amphibolite facies rocks in the Piedmont's King's
Mountain Belt contains deposits of barium sulfate (barite). Barium is especially common as
concretions and vein fillings in limestone and dolostone, which are not common geologic rocks
in the North Carolina Piedmont; however, at various times in the past century and a half, the
Carolinas have been major producers of barite (USEPA 2014).
In a statistical summary of groundwater quality in North Carolina, the Superfund Research
Program at UNC analyzed private well water samples in North Carolina. These samples were
tested by the North Carolina State Laboratory of Public Health from 1998-2010. Since the Buck
site is located near the border of Rowan and Davidson counties, statistics for both are included
here. Data collected from 1,042 private wells across Rowan and Davidson counties from 1998-
2010 indicated that no samples had barium concentrations exceeding the primary MCL of 2,000
pg/L (NC DHHS 2010). The summary statistics for both counties are provided in Table 10-2.
10.1.4 Boron
While boron is relatively abundant on the earth's surface, boron and boron compounds are
relatively rare in all geological provinces of North Carolina. Natural sources of boron in the
environment include volatilization from seawater, geothermal vents, and weathering of clay -rich
sedimentary rocks. Total contributions from anthropogenic sources are less than contributions
from natural sources. Anthropogenic sources of boron include agriculture, refuse, coal and oil -
burning power plants, by-products of glass manufacturing, and sewage and sludge disposal
(EPRI 2005).
Boron is usually present in water at low concentrations. Surface waters typically have
concentrations of 0.001 to 5 mg/L, with an average concentration of about 0.1 mg/L.
Background boron concentrations in groundwater near power plants were compiled from data
presented in EPRI technical reports, and ranged from <0.01 to 0.59 mg/L with a median
concentration of 0.07 mg/L (EPRI 2005).
10.1.5 Chromium
Chromium is a blue -white metal found naturally only in combination with other substances. It
occurs in rocks, soil, plants, and volcanic dust and gases (EPRI 2008) Background
concentrations of chromium in groundwater generally vary according to the media in which they
occur. Most chromium concentrations in groundwater are low, averaging less than 1.0 pg/L
worldwide. Chromium tends to occur in higher concentrations in felsic igneous rocks (such as
granite and metagranite) and ultramafic igneous rocks; however, it is not a major component of
the igneous or metamorphic rocks found in the North Carolina Piedmont or the Blue Ridge
(Chapman 2013).
In a statistical summary of groundwater quality in North Carolina, the Superfund Research
Program at UNC analyzed private well water samples in Rowan and Davidson counties. The
samples were tested by the North Carolina State Laboratory of Public Health from 1998-2010.
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This study found average chromium concentrations were 5.6 pg/L and 5.3 pg/L in Rowan and
Davidson counties, respectively (NC DHHS 2010). Statistics for both counties are included in
Table 10-2.
10.1.6 Cobalt
The concentration of cobalt in surface and groundwater in the United States is generally low —
between 1 and 10 parts of cobalt in 1 billion parts of water (ppb) in populated areas. The
concentration may be hundreds or thousands of times higher in areas that are rich in cobalt -
containing minerals or in areas near mining or smelting operations. In most drinking water,
cobalt levels are less than 1 to 2 ppb (USGS 1973). Cobalt is compared to IMAC since no 2L
Standard has been established for this constituent by NCDENR.
10.1.7 Iron
Iron is a naturally occurring element that may be present in groundwater from the erosion of
natural deposits (NC DHHS 2010). According to Harden (2009), iron commonly exceeds state
and federal regulatory standards in North Carolina groundwater. Iron exceedances occurred in
over half of the state's 10 geozones. The average concentration of iron detected in North
Carolina private well water from sampling conducted in 2010 (NC DHHS 2010) is shown in
Figure 10-2. A study by the Superfund Research program at UNC found that only 15 of the 100
counties in North Carolina had average concentrations below the SMCL of 300 pg/L. The
average iron concentrations in Rowan and Davidson counties were 125,698 pg/L and 531 pg/L,
respectively (Table 10-2).
A 2015 study by DENR (Summary of North Carolina Surface Water Quality Standards 2007-
2014) found that while concentrations vary regionally, "iron occurs naturally at significant
concentrations in the groundwaters of NC," with a statewide average concentration of 1,320
pg/L. The study found the regional variations summarized in Table 10-3.
10.1.8 Manganese
Manganese is a naturally occurring silvery -gray transition metal that resembles iron, but is more
brittle and is not magnetic. It is found in combination with iron, oxygen, sulfur, or chlorine to form
manganese compounds. Manganese occurs naturally in soils, saprolite, and bedrock and is
thus a natural component of groundwater (EPRI 2008).
Manganese concentrations tend to cluster by soil system and geozone throughout North
Carolina, as shown in Figure 10-3. The Carolina Slate and Milton geozones have the highest
proportions of manganese-exceedances, although six other geozones exceeded the state
standard as well (Gillespie 2013). Geozones with magmatic -arc rocks and low-grade
metamorphic rocks, seen in Figure 10-3, tend to include abundant manganese -bearing mafic
minerals likely to contribute manganese for subsurface water cycling (Gillespie 2013). These
rock types are distributed throughout North Carolina and contribute to spatial variations of
manganese concentrations throughout the state. High manganese concentrations are
associated with silty soils, and sedimentary, unconsolidated, or weathered lithologic units. Low
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concentrations are associated with non -weathered igneous bedrock and soils with high
hydraulic conductivity (Polizzotto 2014, Gillespie 2013).
Manganese is most readily released to the groundwater through the weathering of mafic or
siliceous rocks (Gillespie 2013). When manganese -bearing minerals in saprolite, such as biotite,
are exposed to acidic weathering, the metal can be liberated from the host -mineral and released
to groundwater. It can then migrate through pre-existing fractures during the movement of
groundwater through bedrock. If this aqueous -phase manganese is exposed to higher pH in the
groundwater system, it will precipitate out of solution. This results in preferential pathways
becoming "coated" in manganese oxides and introduces a concentrated source of manganese
into groundwater (Gillespie 2013).
Manganese (II) in suspension of silt or clay is commonly oxidized by microorganisms present in
soil, leading to the precipitation of manganese minerals (ATSDR 2012).
Roughly 40-50% of North Carolina wells have manganese concentrations higher than the state
drinking water standard (Gillespie 2013). Concentrations are spatially variable throughout the
state, ranging from less than 0.01 mg/L to more than 2 mg/L. This range of values reflects
naturally derived concentrations of the constituent and is largely dependent on the bedrock's
mineralogy and extent of weathering (Gillespie 2013).
In a 2015 study by DENR (Summary of North Carolina Surface Water Quality Standards 2007-
2014) it was found that concentrations vary regionally, however "manganese occurs naturally at
significant concentrations in the groundwater of NC," with a statewide average concentration of
102 pg/L. The study found the regional variations summarized in Table 10-3.
Using the USGS National Uranium Resource Evaluation (NURE) database, all manganese tests
within a 20-mile radius of the Buck site are shown on Figure 10-4. These samples were taken at
depths ranging from 7-360 feet bgs, and the manganese concentrations ranged from below
detection limits to 439.9 pg/L. Manganese concentrations in the three locations nearest to the
Buck site are less than the SMCL and 2L Standard of 50 pg/L.
10.1.9 Nickel
Nickel is a hard, lustrous, silvery -white metal that resists corrosion. It occurs in all types of soils,
and is frequently in rocks and underwater sediments (EPRI 2008). Nickel combines easily with
other metals to form mixtures called alloys. For example, nickel mixed with steel forms stainless
steel, a common alloy that resists rust and corrosion. The U.S. nickel coin contains 25% nickel
mixed with copper. Nickel and its alloys are also used in batteries, spark plugs, electrical
resistance wires, metal jewelry, cookware, and textile dyes (EPRI 2008).
While nickel can exist in oxidation states -1 through +4, the only important oxidation state is
Ni(II) under normal environmental conditions (EPRI 2008).
Sulfide deposits are by far the most important present source of nickel, in regard to both
quantity of nickel and number of deposits; however, North Carolina's nickel is frequently found
in iron and aluminum -rich soil called laterite (USGS 1973, Horton et al. 1991). Laterite is formed
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by the weathering of iron- and magnesium -rich rocks in humid, tropical to sub -tropical areas.
The repeated processes of dissolution and precipitation lead to a uniform dispersal of nickel that
is not amenable to concentration by physical means; therefore, these ores are concentrated by
chemical means such as leaching (ATSDR 2012).
There has been interest in a few small residual nickel laterites in the Blue Ridge Mountains
geologic province of southwestern North Carolina. The nickeliferous soils form above alpine
peridotites and duniites. In general, the anomalous nickel values (as high as 1 to 3% nickel)
consist of garnierite and genthite in small veinlets in lateritic soils and in the upper portion of
underlying bedrock. The veinlets themselves run as high as 10% nickel. The largest
concentration is found in one million tons of 1 % nickel soils near Webster, North Carolina
(Horton et al. 1991). Despite this abundance, there are no nickel mining operations currently in
the U.S., as U.S. supplies are imported or recycled (ATSDR 2012).
Nickel is a natural constituent of soil and is transported into streams and waterways in runoff
either from natural weathering or from disturbed soil. Much of this nickel is associated with
particulate matter. Nickel also enters bodies of water through atmospheric deposition (ATSDR
2012). The primary source of nickel in drinking -water is leaching from metals in contact with
drinking -water, such as pipes and fittings (WHO 2007).
Nickel concentrations in groundwater depend on the soil use, pH, and depth of sampling. Once
nickel is in surface and ground water systems, physical and chemical interactions
(complexation, precipitation/dissolution, adsorption/desorption, and oxidation/reduction) occur
that will determine its fate and that of its constituents (USEPA 2009). Acid rain increases the
mobility of nickel in the soil and thus might increase nickel concentrations in groundwater (WHO
2007).
10.1.10 Selenium
Selenium is a semi -metallic gray metal that commonly occurs naturally combined with rocks and
soil. It is common to find trace amounts of selenium in food, drinking water, and air -borne dust.
Over geologic time, selenium has been introduced to the earth's surface and atmosphere
through volcanic emissions and igneous extrusions. Weathering and transport partition the
element into residual soils, where it is available for plant uptake, or to the aqueous environment,
where it may remain dissolved, enter the aquatic food chain, or redeposit within a sedimentary
rock such as shale (EPRI 2008).
Groundwater containing selenium is typically the result of either natural processes or industrial
operations. Naturally, selenium's presence in groundwater is from leaching out of selenium -
bearing rocks. It is most common in shale ranging from 0.6 to 103 mg/kg. Anthropogenically,
selenium is released as a function of the discharge from petroleum and metal refineries and
from ore mining and processing facilities. Ore mining may enhance the natural erosive process
by loosening soil, creating concentrations in erodible tailings piles, and exposing selenium
containing rock to runoff (Martens 2002, USEPA 2014).
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In a statistical summary of groundwater quality in North Carolina, the Superfund Research
Program at UNC analyzed 1,040 private well water samples in Rowan and Davidson counties
from 1998-2010. The concentrations ranged from 2.5 to 74.3 pg/L, and one sample exceeded
the 50 pg/L primary MCL for selenium. The mean selenium concentration measured in these
counties was 2.7 pg/L (NC DHHS 2010). Selenium summary statistics are reported in Table 10-
2.
10.1.11 Sulfate
Sulfates are naturally occurring substances that are found in minerals, soil, and rocks. They are
present in ambient air, groundwater, plants, and food. The principal commercial use of sulfate is
in the chemical industry. Sulfates are discharged into water in industrial wastes and through
atmospheric deposition (USEPA 2003).
While sulfate has a SMCL, and no enforceable maximum concentration set by the USEPA,
ingestion of water with high concentrations of sulfate may be associated with diarrhea,
particularly in susceptible populations, such as infants and transients (USEPA 2012).
In the Piedmont and Blue Ridge Aquifers chapter of the USGS Groundwater Atlas of the United
States, the groundwater of this region as a whole is described as "generally suitable for
drinking... but iron, manganese, and sulfate locally occur in objectionable concentrations,"
(USGS 1997).
10.1.12 TDS
Groundwater contains a wide variety of dissolved inorganic constituents as a result of chemical
and biochemical interactions between the groundwater and the elements in the soil and rock
through which it passes. Total Dissolved Solids (TDS) mainly consist of cation and anion
particles (e.g., calcium, chlorides, nitrate, phosphorus, iron, sulfur, and others) that can pass
through a 2 micron filter (USEPA, 1997). TDS is therefore a measure of the total amount of
dissolved ions in the water, but does not identify specific constituents, or explain the nature of
ion relationships.
TDS concentrations in groundwater can vary over many orders of magnitude and generally
range from 0 — 1,000,000 µg/L. The ions listed below are referred to as the major ions as they
make up more than 90 percent of the TDS in groundwater. TDS concentrations resulting from
these constituents are commonly greater than 5,000 µg/L (Freeze and Cherry, 1979).
• Sodium (Na')
• Magnesium (Mg2+)
• Calcium (Ca2+)
• Chloride (CI-)
• Bicarbonate (HCO3 )
• Sulfate (SO42-)
Minor ions in groundwater include: boron, nitrate, carbonate, potassium, fluoride, strontium,
and iron. TDS concentrations resulting from minor ions typically range between 10 — 1,000 µg/L
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(Freeze and Cherry, 1979). Trace constituents make up an even smaller portion of TDS in
groundwater and include: aluminum, antimony, arsenic, barium, beryllium, cadmium, chromium,
cobalt, lead, manganese, nickel, selenium, thallium, vanadium, and zinc among others. TDS
concentrations resulting from trace constituents are typically less than 100 µg/L (Freeze and
Cherry, 1979). In some cases, contributions from anthropogenic sources can cause some of the
elements listed as minor or trace constituents to occur as contaminants at concentration levels
that are orders of magnitude above the normal ranges indicated above.
Because TDS is not considered a hazard to human health, it has no USEPA-defined MCL. The
USEPA has established an SMCL for TDS because elevated levels are associated with
negative aesthetic effects, such as taste and odor of drinking water. Water containing more than
2,000,000 — 3,000,000 µg/L TDS is generally too salty to drink (the TDS of seawater is
approximately 35,000,000 µg/L) (Freeze and Cherry, 1979).
In the April 2015 CCR Rule, the USEPA listed TDS as an indicator constituent (along with
boron, calcium, chloride, fluoride, pH, and sulfate). USEPA defines indicator constituents as
those that are present in CCR and would rapidly move through the surface layer, relative to
other constituents, and thus provide an early detection of whether contaminants are migrating
from the CCR unit (USEPA CCR Rule, 2015).
10.1.13 Thallium
Pure thallium is a soft, bluish white metal that is widely distributed in trace amounts in the
earth's crust. In its pure form, it is odorless and tasteless. It can be found in pure form or mixed
with other metals in the form of alloys. It can also be found combined with other substances
such as bromine, chlorine, fluorine, and iodine to form salts (EPRI 2008).
Traces of thallium naturally exist in rock and soil. As rock and soil is eroded, small amounts of
thallium end up in groundwater. In a USGS study of trace metals in soils, the variation in
thallium concentrations in A (i.e., surface) and C (Le, substratum) soil horizons was estimated
across the United States. The overall thallium concentrations range from <0.1 mg/kg to 8.8
mg/kg. North Carolina concentrations from this study are depicted in Figure 10-5. Thallium is
compared to an IMAC since no 2L Standard was established for this constituent by NCDENR.
In a study by the Georgia Environmental Protection Division (EPD) of the Blue Ridge Mountain
and Piedmont aquifers, 120 sites were sampled for various constituents. Thallium was not
detected at any of these sites (MRL=1 pg/L) (Donahue 2007).
10.1.14 Vanadium
Vanadium is widely distributed in the earth's crust at an average concentration of 100 ppm
(approximately 100 mg/kg), similar to that of zinc and nickel. Vanadium is the 22nd most
abundant element in the earth's crust. Occurrence of vanadium in groundwater is known to be
limited to its soluble oxidation state, V(V). In their study on regional distribution of vanadium in
groundwater, Wright et al. (2010) found that high levels of vanadium in groundwater were
almost always associated with oxic and alkaline groundwater conditions. Vanadium is compared
an IMAC of 0.3 pg/L since no 2L Standard has been established for this constituent by
NCDENR.
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In a study by the Georgia EPD, 120 sites in the Blue Ridge and Piedmont physiographic regions
(regions shared with North Carolina) were sampled and detectible traces of vanadium were
found in six samples (with a reporting limit of 10 tag/L). Only two of these samples were in basic
pH groundwater while the rest were sampled in more acidic waters (see Figure 10-6).
Using the USGS NURE database, all vanadium tests within a 20-mile radius of the Buck site are
shown on Figure 10-6. Concentrations in this region range from <0.10 to 42.9 pg/L.
10.1.15 pH
The pH scale is used to measure acidity or alkalinity. A pH value of 7 indicates neutral water. A
value lower than the USEPA-established SMCL range (<6.5 Standard Units) is associated with
bitter, metallic tasting water, and corrosion. A value higher than the SMCL range (>8.5 Standard
Units) is associated with a slippery feel, soda taste, and deposits in the water (USEPA, 2013).
In a statistical summary of groundwater quality in North Carolina, the Superfund Research
Program at UNC analyzed 2,341 private well water samples for pH in Rowan and Davidson
counties. The samples were analyzed by the North Carolina State Laboratory of Public Health
from 1998-2010. This study found that 13.74% of wells in Rowan County and 20.25% of wells in
Davidson County had a pH result outside of the EPA's SMCL range (NC DHHS 2010).
Using the USGS NURE database, pH values within a 20-mile radius of the Buck site generally
ranged between 6.01 and 8.0.
10.2 Background Wells
Background (BG) monitoring well locations were identified based on the SCM at the time the
Work Plan was submitted. The BG locations were selected to be installed in areas of the site
that are topographically upgradient and assumed not to be impacted by the ash basin and ash
storage area. Based on the groundwater contours (Figures 6-7 through 6-9) and the updated
SCM, the BG locations are considered to be hydrologically upgradient of the ash basin and ash
storage area. Therefore, the BG monitoring well locations are considered to be representative of
background groundwater quality conditions at the Buck site.
BG monitoring wells include two existing groundwater monitoring wells MW-6S/D, and seven
newly installed groundwater monitoring wells BG-1 S/D/BR, BG-2S/D, and BG-3S/BRU. BG
monitoring wells are depicted on Figure 10-7. Well construction details are summarized in
Tables 6-8 and 6-9. A generalized well construction diagram for newly installed wells is shown
on Figure 10-8. Well installation procedures are documented in Appendix G, along with
variances from the Work Plan. Boring logs are provided in Appendix H.
BG wells MW-6S/D were installed in 2006 as compliance monitoring wells to evaluate
background water quality at the site and are located at the southern extent of the ash basin
compliance boundary. MW-6S was installed to a depth of 28 feet bgs and screened from 18 to
28 feet bgs. MW-6D was installed to a depth of 108.5 feet bgs and screened from 103.5 to
108.5 feet bgs. Groundwater flow in the vicinity of MW-6S/D is to the northeast towards the ash
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basins and to the Yadkin River. Historical groundwater data for MW-6S/D dates back to
November 2006. The compliance monitoring wells are sampled three times a year (January,
May, and September) and 20 sampling events have been conducted to date. This is considered
sufficient data to adequately perform statistic analysis of the background concentrations (see
Appendix G). Duke Energy recognizes that the NCDENR DWR Director is responsible for
establishing site -specific background levels for groundwater as stated in 15A NCAC 02L
.0202(a)(3). The concentrations in the statistical report are provided as information to aid in this
determination, and for comparative purposes for groundwater at the site.
Monitoring well MW-6S had antimony (dissolved fraction) and cobalt reported at concentrations
greater than their IMACs. Monitoring well MW-6D had vanadium reported at a concentration
exceeding the IMAC. Concentrations of arsenic and boron were less than the laboratory
reporting limits for the samples collected from both of these wells. Concentrations of chloride,
calcium, and sulfate were reported at concentrations similar to or less than the newly installed
background wells. The existing background monitoring well results do not exhibit ash related
constituents at elevated levels compared to the porewater sample results and the ash basin
water results. The concentrations of constituents associated with coal ash in monitoring wells
MW-6S and MW-6D are similar to, or less than, the concentrations reported in the newly
installed background wells.
Newly installed background monitoring wells BG-1 S/D/BR, BG-2S/D, and BG-3S/BRU were
installed to evaluate background water quality in the regolith, TZ, and bedrock. BG-1 S was
installed to 30 feet bgs and screened from 15 to 30 feet bgs. BG-1 D was installed to 104 feet
bgs and screened from 99 to 104 feet bgs. BG-1 BR was installed to 141 feet bgs and screened
from 136 to 141 feet bgs; however, the well had insufficient water in the well at the time of
sampling to collect a groundwater sample. BG-2S was installed to 32.10 feet bgs and screened
from 17.10 to 32.10 feet bgs. BG-2D was installed to 104 feet bgs and screened from 99 to 104
feet bgs. BG-3S was installed to 40.30 feet bgs and screened from 25.30 to 40.30 feet bgs. BG
3BRU was installed to 75 feet bgs and screened from 70 to 75 feet bgs.
Currently, insufficient data is available to qualify BG-1 S/D/BR, BG-2S/D, and BG-3S/BRU as
background monitoring wells and provide associated statistical analysis. As data become
available, statistical analysis will be performed and determination made as to whether these
wells qualify as background monitoring wells.
Based on review of available information, the number of background wells located within the
property boundary of the site is adequate for monitoring background groundwater quality;
however, background monitoring well BG-1 BR may not be a viable bedrock background well
due to the lack of water in the well at the time of sampling. A replacement bedrock background
well may be necessary if BG-1 BR continues to produce inadequate amounts of water for
sample collection. The background wells are located hydrologically upgradient and were
strategically placed to maximize physical separation from the ash basin and ash storage area.
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10.3 Discussion of Redox Conditions
Determination of the reduction/oxidation (redox) condition of groundwater is an important
component of groundwater assessments, and helps to understand the mobility, degradation,
and solubility of contaminants. By applying the framework of the Excel Workbook for Identifying
Redox Processes in Ground Water (Jurgens, McMahon, Chapelle, and Eberts 2009) to the
analytical results in the following sections, the predominant redox process or category was
assigned to samples collected during the groundwater assessment. Categories include oxic,
suboxic, anoxic, and mixed. Assignment of redox category was based upon concentrations of
DO, nitrate as nitrogen, manganese (II), iron (II), sulfate, and sulfide as inputs. Constituent
criteria appropriate for inputs to the Excel Workbook, as well as an explanation of the redox
assignments, can be found in Tables 1 and 2, respectively, of the USGS Open File Report
2009-1004 (Jurgens, et al. 2009).
Redox assignment results are presented in Table 10-4.
10.4 Groundwater Analytical Results
A total of 64 groundwater monitoring wells were installed at Buck between March and July 2015
as part of the groundwater assessment program. Groundwater monitoring well locations are
shown on Figure 10-7. Monitoring well information is provided in Tables 6-8 and 6-9. Monitoring
wells were installed in general accordance with procedures described in the Work Plan and a
detailed description is provided in Appendix H. Boring logs and field parameters are also
provided in Appendix H.
Groundwater sample results are compared to the North Carolina 2L Standards and IMACs.
Background groundwater sample field parameters and laboratory analytical results for totals and
dissolved constituents are summarized in Table 10-5 and background speciation groundwater
laboratory results are summarized in Table 10-7. Groundwater sample field parameters and
laboratory results for totals and dissolved constituents are summarized in Table 10-6 and
assessment well groundwater speciation laboratory results are summarized in Table 10-8.
Groundwater sampling results are depicted on Figure 10-9. Variances from the proposed
sampling plans are presented in Appendix G. Field and sampling quality control / quality
assurance protocols are provided in Appendix E.
Duke Energy conducted speciation of groundwater samples for arsenic, chromium, iron,
manganese, and selenium from selected wells along inferred groundwater flow transects.
Speciation results for background groundwater and groundwater samples are provided in the
above referenced tables and the remaining results will be included in the CSA supplement.
Well designations and descriptions for the installed assessment monitoring wells include:
• AB - Ash Basin — Monitoring wells installed to provide water quality data in and beneath
the ash basins and ash basin dikes.
• AS — Ash Storage Area — Monitoring wells installed to provide water quality data beneath
the ash storage area.
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• GWA — Groundwater Assessment — Monitoring wells installed outside of the waste
boundary for use in groundwater modeling (i.e., to evaluate the horizontal and vertical
extent of potentially impacted groundwater outside the waste boundary).
• BG — Background — Monitoring wells installed to provide information on background
water quality.
• S — Shallow - Monitoring wells installed in regolith or ash that were screened to bracket
the water table surface at the time of installation.
• SL — Shallow Lower - Monitoring wells installed with the bottom of the well screen set
above the ash-regolith interface.
• D — Deep - Monitoring wells installed with the screened interval within the partially
weathered/fractured bedrock transistion zone at the base of the regolith.
• BRU — Bedrock Upper - Monitoring wells that were originally proposed to be "D" wells;
however, a partially weathered/fractured bedrock transition zone was not encountered in
the boring. These wells were screened within the first 15 feet of fresh, competent
bedrock encountered below the regolith.
• BR — Bedrock - Monitoring wells screened across water -bearing fractures within fresh
competent bedrock after continuous coring of at least 50 feet into competent bedrock.
Groundwater monitoring wells were developed prior to sampling activities in general accordance
with well development procedures detailed in Appendix G. The well development forms are also
included in Appendix G. Groundwater samples were collected and analyzed in general
accordance with the procedures and methods described in the Work Plan and in Duke Energy's
Low Flow Sampling Plan, Duke Energy Facilities, Ash Basin Groundwater Assessment
Program, dated May 22, 2015. Refer to Appendix D for a detailed description of these methods.
Appendix D also includes a summary of variances from the well development and sampling
plans. Appendix E includes the field and sampling quality control / quality assurance protocols.
Groundwater samples were collected from background locations, beneath the ash basin,
beneath the ash storage area, and from locations outside the waste boundary. Groundwater
samples were also collected from pre-existing voluntary and compliance wells on the site. Field
parameters are documented in Appendix H.
Groundwater isoconcentration contours with respect to each COI are depicted in Figures 10-10
through 10-51. Cross -sections presenting horizontal and vertical distribution of COls are
depicted on Figures 10-52 through 10-55. COI concentrations along the flow transects will be
modeled in the CAP.
The USEPA recommends that when possible, especially when sampling for constituents that
may be biased by the presence of turbidity, that turbidity values in the stabilized well should be
less than 10 Nephelometric turbidity units (NTUs) (USEPA 2002). Compliance monitoring wells
with analytical results exceeding the 2L Standards have been individually plotted with the
associated turbidity values (Figures 10-105 through 10-143). Maximum contaminant
concentrations for groundwater can be found in Section 17.3.
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10.4.1 Ash Basin
10.4.1.1 Beneath the Ash Basin Waste Boundary
A total of 25 groundwater monitoring wells (8 shallow, 4 shallow lower, 3 deep, 7 upper bedrock,
and 3 bedrock) were installed beneath the ash basin system. These monitoring wells include
AB-1 D, AB-2S/SL/BRU/BR, AB-3S/D, AB-4S/SL/BRU/BR, AB-5S/SL/BRU, AB-6D, AB-
7S/SL/BRU, AB-8S/BRU, AB-9S/BRU/BR, and AB-1 OS/D. These groundwater monitoring wells
were installed to evaluate groundwater quality beneath the ash basin.
Installed groundwater monitoring wells were developed prior to sampling activities in general
accordance with well development procedures detailed in Appendix G. Well development forms
are also included in Appendix G. Groundwater monitoring wells were subsequently collected
and analyzed in general accordance with the procedures and methods described in the Work
Plan and in Duke Energy's Low Flow Sampling Plan, Duke Energy Facilities, Ash Basin
Groundwater Assessment Program, dated May 22, 2015. Any variances from the proposed
development and groundwater sampling plans are included in Appendix G.
Groundwater samples were collected from background locations (described above), locations
upgradient of the ash basin, beneath the ash basin, and downgradient of the ash basin.
Groundwater samples were also collected from select existing voluntary and compliance
monitoring wells. Parameters and constituent analytical methods for the groundwater samples
collected are provided in Table 7-3. Laboratory results for groundwater samples were compared
to 2L Standards and IMACs. Background groundwater results are presented in Table 10-5.
Groundwater sample results (for total and dissolved constituents and other parameters) for
monitoring wells located upgradient of the ash basin (not considered background), beneath the
ash basin, and downgradient of the ash basin are presented in Table 10-6. Field parameters
collected at the time of sampling are provided in Appendix H. Groundwater analytical results for
constituents that exceed 2L Standards or IMACs are depicted on Figure 10-9. Field and
sampling quality control / quality assurance protocols are provided in Appendix E.
10.4.2 Ash Storage Area
A total of 5 groundwater monitoring wells (2 shallow and 3 deep) were installed within the ash
storage area. These monitoring wells include AS-1 S/D, AS-2D, and AS-3S/D. These
groundwater monitoring wells were installed to evaluate groundwater quality beneath the ash
storage area.
10.4.3 Outside the Waste Boundary
A total of 27 groundwater monitoring wells (10 shallow, 8 deep, 5 bedrock upper, and 4
bedrock) were installed outside the waste boundary of the ash basin and ash storage area.
These included wells downgradient, side -gradient and upgradient of the ash basin. These
monitoring wells include the following: GWA-1 S/D, GWA-2D/BRU, GWA-3S/BRU/BR, GWA-
4S/D, GWA-5S/BRU, GWA-6S/BRU/BR, GWA-7S/D, GWA-8D, GWA-9S/D/BR, GWA-10S/D,
GWA-11 S/D, GWA-12S/BRU, and GWA-22D. The groundwater monitoring wells located
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outside the waste boundary, were installed to evaluate the impact of the ash basin and ash
storage area on groundwater quality.
A total of 14 existing groundwater monitoring wells, compliance and voluntary, were sampled to
supplement groundwater quality data for this groundwater assessment. These borings include
the following: MW-3S/D, MW-7S/D, MW-8S/D, MW-9S/D, MW-1OD, MW-11S/D, MW-12S/D,
and MW-13D. Time series plots, time history plots, stacked time series plots and correlation
plots for existing wells are depicted in Figures 10-84 to 10-142.
10.5 Comparison of Results to 2L Standards and IMACs
Groundwater results were compared to their respective 2L Standards or IMACs and
exceedances are summarized below. Table 10-6 and Figure 10-9 present the groundwater
results with exceedances of 2L Standards or IMACs.
10.6 Comparison of Results to Background
10.6.1 Background Wells MW-6S and MW-6D
Background monitoring well MW-6S and MW-6D concentrations were selected for comparison
based on the information presented in Section 10.2, the amount of historical data available, and
a location hydraulically upgradient of the ash basin and ash storage area. With the exception of
antimony, cobalt, iron, manganese, and vanadium, the results for all other constituents have
been reported at less than their respective 2L Standard and IMACs at these wells throughout
their monitoring history. The background concentration ranges for the constituents that are
considered Cols at Buck are provided below. Results with J qualifiers are estimated
concentrations less than the laboratory method reporting limit.
• Antimony 0.58 pg/L to 3.8 pg/L
• Arsenic 0.5U lag/L to 2U lag/L
• Barium
23 pg/L to 86 pg/L
• Boron
50U pg/L
• Chromium
1.1 lag/L to 3.0 pg/L
• Cobalt
0.51J lag/L to 4 pg/L
• Iron
10 pg/L to 1,270 pg/L
• Manganese
15 pg/L to 228 pg/L
• Nickel
0.5U pg/L to 8 pg/L
• Selenium
0.21J lag/L to 0.5U pg/L
• Thallium
0.03J pg/L to 0.2U lag/L
• Vanadium
1.3J lag/L to 9 lag/L
• Sulfate
140 lag/L to 2,400 lag/L
• TDS
21,000 lag/L to 140,000 lag/L
Notes:
pg/L = micrograms per liter
J = Estimated concentration
U = Not detected
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10.6.2 Newly Installed Background Wells
Recently installed background monitoring wells are designated BG-1 S/D/BR, BG-2S/D, and BG-
3S/BRU. Newly installed background wells will be compared to the Buck well network in the
future after additional analysis. With the exception of antimony (one exceedance), chromium
(one exceedance), cobalt (two exceedances), iron (three exceedances), manganese (two
exceedances), and vanadium (six exceedances), the results for all other constituents were
reported at less than the 2L Standards or IMACs. The background concentration ranges in the
newly installed background wells for constituents that are considered COls at Buck are provided
below. Concentrations with J qualifiers are estimated concentrations less than the laboratory
method reporting limits.
•
Antimony
0.23J pg/L to 3.8 pg/L
•
Arsenic
0.26 pg/L to 1 J pg/L
•
Barium
6.4 pg/L to 55 pg/L
•
Boron
38J pg/L to 50U pg/L
•
Chromium
0.42J pg/L to 10.3 pg/L
•
Cobalt
0.15J pg/L to 7.2 pg/L
•
Iron
110 pg/L to 1,900 pg/L
•
Manganese
3.1 J pg/L to 770 pg/L
•
Nickel
0.84 pg/L to 10.9 pg/L
•
Selenium
0.27J pg/L to 0.51LI pg/L
•
Thallium
0.032J pg/L to 0.1 U pg/L
•
Vanadium
0.86J pg/L to 26.6 pg/L
•
Sulfate
860J pg/L to 22,700 pg/L
•
TDS
51,000 pg/L to 175,000 pg/L
Notes:
pg/L =
micrograms per liter
J = Estimated
concentration
U = Not detected
10.6.3 Regional Groundwater Data
The details regarding the regional groundwater data are presented in Section 10.1. Average
chromium concentrations reported for Rowan and Davidson counties were 5.6 pg/L and 5.3
pg/L, respectively. Average iron concentrations reported for Rowan and Davidson counties were
125,698 pg/L and 531 pg/L, respectively. Selenium concentrations reported in Rowan and
Davidson counties ranged from 2.5 pg/L to 74.3 pg/L. Vanadium concentrations reported within
a 20 mile radius of Buck ranged from <0.10 pg/L to 42.9 pg/L. The state of North Carolina
average for manganese is reported at 102 pg/L.
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10.6.4 Groundwater Beneath the Ash Basin
Groundwater monitoring locations beneath the ash basin were obtained from AB-1 D, AB-
2D/BR, AB-31D, AB-4D/BR, AB-5BRU, AB-6BRU, AB-7BRU, AB-8, AB-9S/BRU/BR, and AB-
1 OS/D. The range of COI concentrations along with a comparison to the range of reported
background groundwater in monitoring wells MW-6S and MW-6D and the regional groundwater
data, is provided in Table 10-9.
COls in groundwater beneath the ash basin with concentrations higher than background and/or
regional concentrations include: arsenic, boron, chromium, cobalt, iron, manganese, and
selenium. Antimony, and vanadium concentrations in groundwater beneath the ash basin are
within or below the range of background and/or regional concentrations.
10.6.5 Groundwater Beneath the Ash Storage Area
Groundwater beneath the ash storage area was obtained from monitoring wells AS-1 S/D, AS-
2D, and AS-3S/D. The range of COI concentrations, along with a comparison to the range of
reported background groundwater and the regional groundwater data, is provided in Table 10-
10.
COls in groundwater beneath the ash storage area with concentrations higher than background
and/or regional concentrations include: boron, chromium, cobalt, iron, manganese, nickel,
sulfate, and TDS. Constituents in groundwater beneath the ash storage area with
concentrations that are within or below the range of background and/or regional concentrations
include: antimony, selenium, thallium and vanadium.
10.6.6 Groundwater Beyond the Waste Boundary
Groundwater samples collected from beyond the waste boundary were obtained from MW-
3S/D, MW-7S/D, MW-8S/D, MW-9S/D, MW-10S/D, MW-11 S/D, MW-12S/D, MW-13D, GWA-
1 S/D, GWA-2BRU/BR, GWA-3S/BRU/BR, GWA-4S/D, GWA-5S/BRU, GWA-6S/BRU/BR,
GWA-7S/D, GWA-81D, GWA-9S/D/BR, GWA-10S/D, GWA-11 S/D, GWA-12S/BRU and GWA-
22D. The range of COI concentrations, along with a comparison to the range of reported
background groundwater and the regional groundwater data, is provided in Table 10-11.
To evaluate how COI concentrations varied around and beyond the ash basin waste boundary,
analyses of sampling results for several groupings of monitoring wells were compared to
background monitoring well constituent concentration ranges.
10.6.6.1 Groundwater South of Ash Basin Cell 1
Groundwater monitoring wells located to the south (or upgradient) of Cell 1 include MW-7S/D,
MW-8S/D and GWA-1 S/D. Background well pair MW-6S/D is also located upgradient of and to
the south of Cell 1. Groundwater samples from one or more of these wells exceeded the 2L
Standards or IMACs for chromium, cobalt, iron, manganese, and/or vanadium. Groundwater
samples from the background monitoring wells MW-6S/D exceeded the IMACs for cobalt and
vanadium for the CSA sampling, but had no other exceedances. Groundwater COI
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concentrations for monitoring wells south of Cell 1 were all within or below the background
monitoring well concentration ranges. All of these wells are located within the compliance
boundary.
10.6.6.2 Groundwater West of Ash Basin Cell 1
Groundwater monitoring wells located to the west of Cell 1 include MW-9S/D, GWA-10S/D,
GWA-11 S/D, and GWA-22D. These wells are located between Cell 1 and the stream located to
the west of Cell 1 and are located within the compliance boundary. Groundwater samples from
one or more of these wells exceeded the 2L Standards or IMACs for chromium, cobalt, iron,
manganese, and vanadium. Newly installed background monitoring wells BG-1 S/D and BG-
2S/D are located approximately 2000 feet and topographically upgradient of the southeast end
of Cell 1. Samples from these background monitoring wells exceeded the 2L Standards or
IMACs for antimony, chromium, cobalt, iron, manganese, and vanadium. Groundwater COI
concentrations for wells west of Cell 1 were higher than the background monitoring well
concentration ranges for cobalt and vanadium. All other 2L or [MAC exceedance concentrations
were similar to or below the background monitoring well concentrations. Additional evaluation
related to natural soil/rock mineralogy and chemistry is discussed in Section 14 Data Gaps.
10.6.6.3 Groundwater East of Ash Basin Cells 1, 2, and 3
Groundwater monitoring wells located to the south and east of Cells 2 and 3 are either side -
gradient and/or downgradient to groundwater flow direction near Cells 2 and 3, depending on
location. It is likely that regional groundwater flow is from the divide along Leonard Road
towards Cells 1, 2, and 3, and flow is combined with an element of a local groundwater gradient
with flows from Cell 1 to Cell 2 and on to Cell 3. The measured water levels in wells MW-12S/D
is slightly higher that the water level measured in the adjacent Cell 2, indicating groundwater
flow is towards Ce112. The water measured in MW-13D is slightly higher that the water level
measured in the adjacent Cell 3 indicating groundwater flow is towards Cell 3. Groundwater
samples results in from these two wells exceeded the 2L Standards or IMAC for iron,
manganese, and/or vanadium. Groundwater samples from the background monitoring wells BG-
3S and BG-3BRU also exceeded the 2L Standards or IMAC for these COIs.
Wells GWA2BR and GWABRU are located along the compliance boundary near the dike
between Cell 2 and Cell 3. The water levels measured in these two wells shows an upward
vertical gradient indicating that groundwater in this area is discharging into the ash basin region.
These wells had exceedances of 2L standards or IMACs for antimony, barium, chromium, TDS,
vanadium, and/or iron. Wells GWA-2BRU/BR and GWA-3S/BRU/BR. GWA-2BRU/BR are
located in an area where insufficient data exists to fully evaluate groundwater flow direction (this
data gap is discussed further in Section 14.0).
Wells GWA-3S, GWA-313R, and GWA-3BRU are located to the east of Cell 3 and are
downgradient of Cell 3. These wells are located inside of the compliance boundary on the east
side of a small stream. These wells had exceedances of 2L standards or IMACs for cobalt, iron,
manganese, and/or vanadium. The iron, cobalt, and vanadium concentrations are in the range
of the results from MW-6S/D.
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10.6.6.4 Groundwater North of Ash Basin Cells 1, 2, and 3
Groundwater monitoring wells located to the north of the ash basin are all downgradient of Cells
1, 2, and 3 and generally are located between Cells 1, 2, and 3 and the Yadkin River. These
wells include: GWA-9S/D/BR, GWA-81D, GWA-7S/D, MW-10S/D, GWA-12S/BRU, GWA-
6S/BR/BRU, MW-3S/D, GWA-5S/BRU, MW-11 S/D, and GWA-4S/D. Groundwater samples
from these wells exceeded the 2L Standards or IMACs for antimony, boron, chromium, cobalt,
iron, manganese, sulfate, TDS, and vanadium. The background monitoring wells also exceeded
the 2L Standards or IMACs for all of these COls except boron, sulfate, and TDS.
Boron exceeded the 2L Standard in MW-11 D and in MW-3S (an estimated concentration);
sulfate and TDS exceeded their 2L Standards in GWA-6S/BR/BRU and MW-101D.
Groundwater COI concentrations for downgradient wells north of Cells 1, 2, and 3 were higher
than the background monitoring well concentration ranges for boron, chromium, cobalt, iron,
sulfate, TDS, and vanadium. Source related measured constituent levels above 2L Standards or
IMACs were measured outside the compliance boundary. This includes boron which is shown
on Figure ES-1.
10.6.6.5 Groundwater within Various Layers Beneath the Site
Within the shallow layer (including beneath the ash storage area), there are ten COls identified
in the groundwater within the shallow flow layer (S wells not screened within ash): boron, cobalt,
chromium, iron, manganese, nickel, sulfate, thallium, TDS and vanadium. Chromium, cobalt,
iron, manganese, and vanadium also appear in one or more of the background wells at
concentrations exceeding the applicable 2L Standard or IMACs. Most of these measurements
occurred beneath or within the source and north of the source, with constituents to the north
(above applicable standards and background measurements) being boron, chromium, iron,
manganese, sulfate and TDS. Almost all of the iron exceedances in the shallow layer (12 of 13)
and chromium exceedances (3 of 3) occurred in unfiltered samples indicating the source of the
iron and chromium in the shallow groundwater samples is primarily suspended solids. Six COls
identified in the shallow layer (antimony, boron, nickel, selenium, sulfate, and TDS) are in
isolated locations.
Within the deep flow layer (D wells) (including beneath the ash basin and ash storage area),
there are nine COls identified in the groundwater: antimony, boron, chromium, cobalt, iron,
manganese, sulfate, TDS, and vanadium. Most of these measurements occurred beneath the
source or north of the source, with constituents to the north (above applicable standards and
background measurements) being boron, iron, sulfate, TDS, and vanadium. Almost all of the
iron exceedances within the deep flow layer (10 of 12) occurred within unfiltered samples
indicating the source of the iron within the deep flow layer groundwater samples is primarily
suspended solids. Two of the COls identified in the deep flow layer (sulfate and TDS) are in
isolated locations.
Within the bedrock flow layer (including beneath the ash basin), there are eleven COls in the
groundwater within the bedrock flow layer (BR and BRU wells): antimony, barium, boron,
chromium, cobalt, iron, manganese, selenium, sulfate, TDS and vanadium. Most of these
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measurements occurred north of the source, with constituents to the north (above applicable
standards and background measurements) being sulfate, TDS, and vanadium. None of these
COls appear within the bedrock background well location (BG-3BRU) at a concentration
exceeding the applicable groundwater standard, although it is worth noting that there is little
background information for deep samples and some of the chemical and mineralogical for rock
samples has not been received from the lab for evaluation. All eight of the iron exceedances
within the bedrock flow layer occurred within unfiltered samples indicating the source of the iron
within the bedrock groundwater samples is primarily suspended solids. Six of the COls identified
in the bedrock flow layer (barium, boron, cobalt, selenium, sulfate and TDS) are in isolated
locations. No boron was identified in the bedrock flow layer and sulfate levels may be the result
of natural conditions. This is discussed further in Section 14 Data Gaps.
10.7 Cation and Anion Water Quality Data
Cations and anions are used in hydrogeological investigations to assess naturally occurring ions
in groundwater. Cations are positively charged ions whereas anions are negatively charged
ions. There are eight ions commonly used to evaluate groundwater. These ions consist of four
cations: calcium, magnesium, sodium, and potassium and four anions: chloride, sulfate,
carbonate, and bicarbonate. Geochemical makeup of groundwater aids in aquifer
characterization. Piper diagrams are used to graphically depict geochemistry of groundwater
samples collected at a particular site.
Cation and anion concentrations at Buck from groundwater monitoring wells and ash basin
groundwater monitoring wells are shown in Figures 10-64 and 10-83. In general, calcium and
sulfate are elevated.
Piper diagrams were generated for Buck show comparison of geochemistry between ash basin
porewater, ash basin water, seeps, upgradient and downgradient groundwater monitoring wells
and background groundwater monitoring wells. Ash basin water and ash basin porewater are
generally higher in sulfate and chloride percentages compared to the background groundwater
monitoring wells. Ash basin water tends to have high percentages of sodium and potassium,
while ash basin porewater tends to have a high percentage of calcium. Piper diagrams are
shown in Figures 10-56 to 10-63.
10.8 CCR Rule Groundwater Detection and Assessment
Monitoring Parameters
Appendix III to Part 257 Constituents for Detection Monitoring and Appendix IV to Part
257 Constituents for Assessment Monitoring
On April 17, 2015, the USEPA published its final rule "Disposal of Coal Combustion Residuals
from Electric Utilities" to regulate the disposal of coal combustion residuals (CCR) as solid
waste under subtitle D of the Resource Conservation and Recovery Act (RCRA). Among other
requirements, the final rule establishes requirements for a groundwater monitoring program
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consisting of detection monitoring and, if necessary, assessment monitoring and corrective
action.
USEPA selected constituents to be used in the groundwater detection monitoring program as
indicators of groundwater contamination from CCR. USEPA selected constituents for detection
monitoring that are present in CCR, would be expected to migrate rapidly, and that would
provide early detection as to whether contaminants were migrating from the disposal unit. (80
FIR 74: 21397).
As stated in the FIR (80 FIR 74: 21342):
These detection monitoring constituents or inorganic indicator parameters are:
boron, calcium, chloride, fluoride, pH, sulfate and total dissolved solids (TDS).
These inorganic indicator parameters are known to be leading indicators of
releases of contaminants associated with CCR and the Agency strongly
recommends that State Directors add these constituents to the list of indicator
parameters to be monitored during detection monitoring of groundwater if and
when a MSWLF decides to accept CCR. (Emphasis added)
NCDENR requested that figures be included in the CSA report that depict groundwater
analytical results for the constituents in 40 CFR 257, Appendix III detection monitoring and 40
CFR 257, Appendix IV assessment monitoring.
Detection monitoring constituents in 40 CFR 257 Appendix III are:
• Boron
• Calcium
• Chloride
• Fluoride (this constituent was not analyzed for in the CSA)
• pH
• Sulfate
• TDS
The analytical results for the detection monitoring constituents are found on Figures 10-144 to
10-146.
Constituents for assessment monitoring listed in 40 CFR 257 Appendix IV include:
• Antimony
• Arsenic
• Barium
• Beryllium
• Cadmium
• Chromium
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• Cobalt
• Fluoride (not analyzed for the CSA)
• Lead
• Lithium (not analyzed for the CSA)
• Mercury
• Molybdenum
• Selenium
• Thallium
• Radium 226 and 228 combined
The analytical results for the assessment monitoring constituents are found on Figures 10-147
to 10-149.
Aluminum, copper, iron, manganese, and sulfide were included in the Appendix IV constituents
in the draft rule; USEPA removed these constituents in the final rule. These constituents were
removed because they lack MCLs and were not shown to be constituents of concern based on
either the risk assessment conducted for the CCR Rule or the damage cases reference in the
CCR Rule. Therefore, these constituents are not included on the above referenced figures. In
addition, NCDENR requested that vanadium be included on these figures. Figure 10-9 shows
vanadium as well as other constituents where they exceeded the relevant regulatory standards.
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11.0 Hydrogeological Investigation
The purpose of the hydrogeological investigation is to characterize site hydrogeological
conditions including groundwater flow direction, hydraulic gradient and conductivity,
groundwater and contaminant velocity, and slug test results. The hydrogeological investigation
was performed in general accordance with the procedures described in the Work Plan. Refer to
Appendix H for a description of these methods.
11.1 Hydrostratigraphic Layer Development
The following materials were encountered during the site exploration and are consistent with
material descriptions from previous site exploration studies:
• Ash — Ash was encountered in borings advanced within the ash basin and ash storage
areas, as well as through dikes. Ash was generally described as gray to dark gray,
non -plastic, loose to medium dense, dry to wet, fine to coarse -grained.
• Fill — Fill material generally consisted of re -worked silts, clays, and sands that were
borrowed from one area of the site and re -distributed to other areas. Fill was generally
classified as silty sand, clay with sand, clay, and sandy clay on the boring logs. Fill was
used in the construction of dikes, and as cover for ash storage area.
• Alluvium —Alluvium encountered in borings during the project was classified as clay
and sand with clay. In some cases alluvium was logged beneath ash.
• Residuum (Residual soils) — Residuum is the in -place weathered soil that consists
primarily of silt with sand, clayey sand, sandy clay, clay with gravel, and clayey silts.
Residuum varied in thickness and was relatively thin compared to the thickness of
saprolite.
• Saprolite/Weathered Rock — Saprolite is soil developed by in -place weathering of rock
that retains remnant bedrock structure. Saprolite consists primarily of medium dense to
very dense silty sand, sandy silt, sand, sand with gravel, sand with clay, clay with
sand, and clay. Sand particle size ranges from fine to coarse grained. Much of the
saprolite is micaceous.
• Partially Weathered/Fractured Rock — Partially weathered (slight to moderate) and/or
highly fractured rock encountered below auger refusal.
• Bedrock — Sound rock in boreholes, were generally slightly weathered to fresh and
relatively unfractured.o
Based on the CSA site investigation, the groundwater system is consistent with the regolith-
fractured bedrock system discussed in Section 5.2. To define the hydrostratigraphic units, the
classification system of Schaeffer (2014a) used to show that the TZ is present in the Piedmont
groundwater system (discussed in Section 5-2) was modified to define the hydrostratigraphic
layers of the natural groundwater system. The classification system is based on Standard
Penetration Testing values (N) and the Recovery (REC) and Rock Quality Designation (RQD)
collected during the drilling and logging of the boreholes (Borehole/Well logs in Appendix H).
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The ash, fill, and alluvial layers are as encountered at the site. The natural system (except
alluvium) includes the following layers:
• M1 — Soil/Saprolite: N<50
• M2 — Saprolite/Weathered Rock: N>50 or REC<50%
• TZ — Transition Zone: REC>50% and RQD<50%
• BR — Bedrock: REC>85% and RQD>50%.
Rock core runs that fell between the values for TZ and BR (REC<85% and RQD>50% or
REC>85% and RQD<50%) were assigned a hydrostratigraphic layer based on a review of the
borehole logs, rock core photographs, and geologic judgment. The same review was performed
in making the final determination of the thickness of the TZ as it could extend into the next core
run that meets the BR criterion because of potential core loss or fractured/jointed rock with
indications of water movement (iron/manganese staining).
The above layer designations (M1, M2, TZ, and BR) are used on the geologic cross -sections
with transect locations shown on Figure 11-1. The ash, fill and alluvial layers are represented by
A, F, and S, respectively on the cross -sections and tables.
11.2 Hydrostratigraphic Layer Properties
The material properties required for the groundwater flow and transport model, total porosity,
effective porosity, specific yield and specific storage for ash, fill, alluvium, and soil/saprolite were
developed from laboratory testing (Table 11-1; test data in Appendix H), historic laboratory
testing (Table 1-1 in Appendix H), and published data (Domenico and Mifflin 1965). Table 11-1
has a column labeled `Estimated Specific Yield/Effective Porosity' and the values are estimated
from the laboratory soil data (grain size analysis) utilizing Fetter -Bear diagrams (worksheets in
Appendix H), as described by Johnson (1967) and published data. This technique provides a
simple method to estimate specific yield; however, there are limitations to the method that may
not provide an accurate determination of the specific yield of a single sample (Robson 1993).
Specific yield/effective porosity were determined for a number of samples of the A, F, S, M1,
and M2 layers to provide an average and range of expected values. The effective porosity
(primarily fracture porosity) and specific storage of the TZ and bedrock were estimated from
published data (Sanders 1998; Domenico and Mifflin 1965).
Hydraulic conductivity (horizontal and vertical) of all layers, except vertical hydraulic conductivity
for the TZ and bedrock (BR), was developed utilizing site historic permeability data in -situ
permeability testing (falling head, constant head, and packer testing where appropriate), slug
tests in completed monitoring wells, and laboratory testing of undisturbed samples (ash, fill,
soil/saprolite: test results in Appendix H) during this investigationo
11.2.1 Borehole In -Situ Tests
In -situ horizontal (open hole) and vertical (flush bottom) permeability tests, either falling or
constant head as appropriate, for field conditions, were performed in each of the
hydrostratigraphic units above refusal, ash, fill, alluvium, and soil/saprolite. In -situ borehole
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horizontal permeability tests, either falling or constant head tests as appropriate for field
conditions, were performed just below refusal in the first 5 feet of a rock cored borehole (TZ, if
present).
The flush bottom test involves advancing the borehole through the overburden with a casing
advancer until the test interval is reached. The cutting tool is removed from the casing and the
casing is filled with water to the top and the drop of the water level in the casing is measured
over a time period of 60 minutes. In the open hole test, after the top of the test interval is
reached, the cutting tool but not the casing, is advanced an additional number of feet (five feet
in the majority of tests) and drop of the water level in the casing is measured over a time period
of 60 minutes. The constant head test is similar except the water level is kept at a constant level
in the casing and the water flow -in is measured over a period of 60 minutes. The constant head
test was only used when the water level in the borehole was dropping too quickly back to the
static water level such that the time interval was insufficient to calculate the hydraulic
conductivity. The results from the field permeability testing are summarized in Table 11-2 and
the worksheets are provided in Appendix H.
Packer tests (shut-in and pressure tests) were conducted in a minimum of five boreholes. The
shut-in test is performed by isolating the zone between the packers (in effect, a piezometer) and
measuring the resulting water level over time until the water level is stable. The shut-in test
provides an estimate of the vertical gradient during the test interval. The pressure test involves
forcing water under pressure into rock through the walls of the borehole providing a means of
determining the apparent horizontal hydraulic conductivity of the bedrock. Each interval is tested
at three pressures with three steps of 20 minutes up and two steps of 5 minutes back down. The
pressure test results are summarized in Table 11-2 and the shut-in and packer tests worksheets
are provided in Appendix H.
Where possible, tests were conducted at borehole locations specified in the Work Plan and at
test intervals based on site -specific conditions at the time of the groundwater assessment work.
The U.S. Bureau of Reclamation (1995) test method and calculation procedures, as described
in Chapter 10 of their Ground Water Manual (2nd Edition, were used for the field permeability
and packer tests.
11.2.2 Monitoring Well and Observation Well Slug Tests
Hydraulic conductivity (slug) tests were completed in monitoring wells and observation wells
under the direction of the Lead Geologist/Engineer. Slug tests were performed to meet the
requirements of the May 31, 2007 NCDENR Memorandum titled, Performance and Analysis of
Aquifer Slug Tests and Pumping Tests Policy, . Water level change during the slug tests was
recorded by a data logger. The slug test was performed for no less than 10 minutes, or until
such time as the water level in the test well recovered 95 percent of its original pre-tests level,
whichever occurred first. Slug tests were terminated after 60 minutes even if the 95 percent pre-
test level was not achieved. Slug test field data was analyzed using the Aqtesolv (or similar)
software and the Bouwer and Rice method.
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The slug test results are presented in Table 11-3 and the Slug Test Report is provided in
Appendix H. Historic slug test data is presented in Table 11-4.
11.2.3 Laboratory Permeability Tests
Laboratory permeability tests were conducted on undisturbed samples (Shelby tubes) of ash,
fill, soil, and saprolite collected during the field investigation. The tests were performed in
accordance with ASTM D 5084 (ASTM 2010). Results of the laboratory permeability tests are
presented in Table 11-5 and historic laboratory permeability tests are presented in Table 11-6
11.2.4 Hydrostratigraphic Layer Parameters
The soil material parameters for the A (ash), F (fill), S (alluvium), M1 (soil/saprolite), and M2
(saprolite/weathered rock) were developed by grouping the data into their respective
hydrostratigraphic unit and calculating the mean, median, and standard deviation of the different
parameters. Estimated values for total porosities for the Hydrostratigraphic layers A, F, S, M1,
and M2 are presented in Table 11-7. Values for estimated effective porosity/specific yield are
presented in Table 11-8. The values for specific storage presented in Table 11-8 are based on
published data (Domenico and Mifflin 1965).The hydraulic conductivity parameters were
developed by grouping the data into their respective hydrostratigraphic units and calculating the
geometric mean, median, and standard deviation of the different parameters. Vertical hydraulic
conductivity values are not available for the TZ and BR units, but are unlikely to be equal. As an
initial assumption, vertical hydraulic conductivity for these units can be considered to be equal to
the horizontal hydraulic conductivity and adjusted as necessary during flow model calibration.
Horizontal and vertical hydraulic conductivity parameters are presented Tables 11-9 and 11-10,
respectively. The values of secondary (effective) porosity and specific storage for the TZ and
BR units are based on published values (Sanders 1998; Domenico and Mifflin 1965) and are
presented in Table 11-11.
Further development of the above parameters and others required for the flow and contaminant
transport model will be provided in the CAP.
11.3 Hydraulic Gradients
Horizontal hydraulic gradient is calculated by taking the difference in hydraulic head over the
distance between two wells with similar well construction. Section 6.2.2 provides additional
details for horizontal hydraulic gradients calculated for the site.
Vertical hydraulic gradient was calculated by taking the difference in groundwater elevation in a
deep and shallow well pair over the difference in total well depth of the deep and shallow well
pair. A positive output indicates upward flow and a negative output indicates downward flow.
Thirteen well pair locations, each consisting of a shallow and deep groundwater monitoring well,
were used to calculate vertical hydraulic gradient across the site. Based on review of the results,
vertical gradient of groundwater is generally downward across the site. Vertical gradient
calculations are summarized in Table 11-13.
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11.4 Groundwater Velocity
Darcy's Law is an equation that describes the flow rate or flux of fluid through a porous media.
To calculate the velocity that water moves through a porous medium, the specific discharge, or
Darcy flux, is divided by the effective porosity, ne. The result is the average linear velocity or
seepage velocity of groundwater between two points.
The following equation was used to calculate groundwater velocities through each
hydrostratigraphic unit present at the site:
v = Ki
ne
where vis velocity; Kis horizontal hydraulic conductivity; i is
horizontal hydraulic gradient; and ne is the effective porosity
Seepage velocities for groundwater were calculated using horizontal hydraulic gradients
established in Section 6.2.2, horizontal hydraulic conductivity values for each hydrostratigraphic
unit established in Table 11-9 and effective porosity values established in Tables 11-8 and 11-
11. Hydrostratigraphic layers are defined in Section 11.1. Average groundwater seepage
velocity results are summarized in Table 11-12. The rate of groundwater migration varies with
the hydraulic conductivity and porosity of the site soil and rock materials and ranged from 5.3
ft/yr to 91.8 ft/yr in soils, and 4.0E+2 ft/yr to 2.29E+5 ft/yr in rock.
11.5 Contaminant Velocity
Contaminant velocity depends on factors such as; the rate of groundwater flow, the effective
porosity of the flow layer material, and the soil -water partition coefficient, or Kd term. Site
specific Kd terms will be developed using samples collected during the site investigation. The
testing to develop the Kd terms is still underway and the results will be presented in the CAP.
The groundwater modeling to be performed in the CAP will present the velocities for the
modeled contaminants.
11.6 Plume's Physical and Chemical Characterization
Plume physical and chemical characterization is detailed below for each constituent detected in
porewater and groundwater samples, and is based on the isoconcentration maps (Figures 10-
10 through 10-51 and cross sections (Figures 8-2 through 8-4). These descriptions are based
on a single groundwater sampling event described in the approved Work Plan, both unfiltered
and filtered (0.45 pm filter) samples were collected for analyses of constituents whose results
may be biased by the presence of turbidity.3 Unless otherwise noted, concentration results
discussed are for the unfiltered samples and represent total concentrations.
3 The USEPA (EPA 2002) recommends that when possible, especially when sampling for contaminants
that may be biased by the presence of turbidity, the turbidity reading is desired to stabilize at a value
below 10 Nephelometric Turbidity Units (NTUs)
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• Antimony concentrations were not reported above the IMAC in monitoring wells screened
within the shallow flow layer except at background locations BG-1 S and MW-6S. Antimony
concentrations in monitoring wells screened within the deep flow layer exceeded the IMAC
within the ash storage area at AS-2D and north of the ash basin compliance boundary at
GWA-7D. Antimony concentrations in the bedrock flow layer exceeded the IMAC within ash
basin Cells 2 and 3 at AB-4BR, AB-6BRU, AB-7BRU, and AB-9BRU, as well as near the
compliance boundary east of Cell 2 at GWA-2BR and GWA-2BRU.Wells within the bedrock
flow layer had more exceedances than wells within the deep and shallow flow layer.
• Arsenic concentrations were not reported above 2L Standards in monitoring wells screened
within the shallow or deep flow layers. Arsenic concentration in monitoring wells screened
within the bedrock flow layer exceeded the 2L Standards within ash basin Cell 2 at AB-4BR
only.
• Barium concentrations were not reported above 2L Standards in monitoring wells screened
within the shallow flow layer or deep flow layer. Barium concentrations in monitoring wells
screened within the bedrock flow layer exceeded the 2L Standards near the compliance
boundary east of ash basin Cell 2 at GWA-2BR only.
• Boron concentrations in monitoring wells screened within the shallow flow layer exceeded the
2L Standard beneath the ash storage area at AS-1 S and at voluntary well MW-3S located
near the toe of the ash basin Cell 2/3 main dam. Boron concentrations in monitoring wells
screened within the deep flow layer exceeded the 2L Standard within ash basin Cell 1 at AB-
1 D and AB-1 OD, and at compliance well MW-11 D located at the toe of the ash basin Cell 2/3
main dam. Boron concentrations in monitoring wells screened within the bedrock flow layer
exceeded the 2L Standards at AB-9BRU near the ash basin Cell 2/3 main dam.
• Chromium concentrations in monitoring wells screened within the shallow flow layer
exceeded the 2L Standard at background well BG-1 S; near the compliance boundary north of
ash basin Cell 2 at GWA-6S and GWA-7S; and near the compliance boundary west of ash
basin Cell 1 at GWA-11 S. Chromium concentrations in the S wells generally exhibited a
significant difference between unfiltered and filtered concentrations, indicating that some
exceedances may be related to turbidity. Chromium concentrations in monitoring wells
screened within the deep flow layer exceeded the 2L Standard within ash basin Cell 1 at AB-
1 OD, beneath the ash storage area at AS-31D, near the compliance boundary west of ash
basin Cell 1 at GWA-11 D, and near the compliance boundary south of Cell 1 at GWA-1 D.
Chromium concentrations in monitoring wells screened within the bedrock flow layer
exceeded the 2L Standards within ash basin Cells 2/3 at AB-6BRU, AB-7BRU, and AB-9BR;
and near the compliance boundary east of Cell 2 at GWA-2BR.
Cobalt concentrations in monitoring wells screened within the shallow flow layer exceeded
the 2L Standard at all locations, including the background locations, with the exception of
GWA-1 S, GWA-1OS, MW-7S, MW-9S, and, MW-12S. Cobalt concentrations in monitoring
wells screened within the deep flow layer exceeded the IMAC beneath the ash storage area
at AS-2D; near the compliance boundary north of ash basin Cell 1 at GWA-81D, GWA-91D, and
GWA-22D; near the compliance boundary south of Cell 1 at MW-7D and MW-8D; and near
the compliance boundary north of ash basin Cell 3 at GWA-41D. Cobalt concentrations in
monitoring wells screened within the bedrock flow layer exceeded the IMAC within ash basin
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Cell 2 at A13-613RU and near the compliance boundary north of Cell 2 at GWA-613RU. Cobalt
has more exceedances in the shallow flow layer than in the deep and beadrock flow layer.
• Iron concentrations in monitoring wells screened within the shallow flow layer exceeded the
2L Standard at all locations with the exception of BG-2S, MW-6S, MW-9S, MW-12S, AS-1 S,
GWA-1 S, and GWA-10S. Iron concentrations in monitoring wells screened within the deep
flow layer exceeded the 2L Standard beneath the ash storage area at AS-21D and AS-31D;
near the compliance boundary north of ash basin Cell 1 at MW-91D, GWA-81D, and GWA-9D;
near the compliance boundary south of Cell 1 at MW-71D and MW-8D; near the compliance
boundary north of ash basin Cell 3 at GWA-4D; and near the compliance boundary west of
ash basin Cell 2 at GWA-71D. Iron concentrations in monitoring wells screened within the
bedrock flow layer exceeded the 2L Standards within ash basin Cell 2 at AB-413RU, AB-
613RU, and AB-9BR; within ash basin Cell 3 at A13-713RU; near the compliance boundary east
of Cell 3 at GWA-313RU; near the compliance boundary east of Cell 3 at GWA-2BRU; and
near the compliance boundary north of Cell 2 at GWA-513RU and GWA-6BRU. Iron exhibited
a significant difference between unfiltered and filtered analyses, indicating that
turbidity/suspended solids may be affecting unfiltered iron analyses.
• Manganese concentrations in monitoring wells screened within the shallow flow layer
exceeded the 2L Standard at all locations with the exception of BG-3S, MW-6S, MW-7S,
MW-9S, GWA-1 S, and GWA-10S. Manganese concentrations in monitoring wells screened
within the deep flow layer exceeded the 2L Standard beneath the ash storage area at AS-21D;
within ash basin Cell 1 at AB-2D; near the compliance boundary south of Cell 1 at MW-7D;
near the compliance boundary north of Cell 1 at GWA-81D, GWA-91D, and GWA-22D; and
near the compliance boundary north of ash basin Cell 2 at MW-10D. Manganese
concentrations in monitoring wells screened within the bedrock flow layer exceeded the 2L
Standard within ash basin Cell 2 at AB-613RU; within ash basin Cell 3 at A13-713RU; and north
of Cell 2 at GWA-513RU, GWA-6BRU, and GWA-12BRU. Manganese concentrations
generally tend to be highest in shallow wells on the northern portion of the site. Manganese
generally tends to be higher in S wells than in D/BR wells across the site.
• Nickel concentrations in monitoring wells screened within the shallow flow layer exceeded the
2L Standard within the ash storage area at AS-1S. No other excedances of nickel were noted
within the deep or bedrock flow layer monitoring wells.
• Selenium concentrations in monitoring wells screened within the shallow flow layer exceeded
the 2L Standard within the ash storage area at AS-1 S. There were no selenium
concentrations exceeding the 2L Standard in monitoring wells screened within the deep flow
layer. Selenium concentrations in monitoring wells screened within the bedrock flow layer
exceeded the 2L Standards within ash basin Cell 2 at A13-413R.
• Sulfate concentrations in monitoring wells screened within the shallow flow layer exceeded
the 2L Standard within the ash storage area at AS-1 S and near the compliance boundary
north of ash basin Cell 2 at GWA-6S. Sulfate concentrations in monitoring wells screened
within the deep flow layer exceeded the 2L Standard near the compliance boundary north of
ash basin Cell 2 at MW-10D. Camparing the ionic composition of groundwater samples from
GWA-6S and MW-10D to ash porewater samples (see Section 10.7) indicates the
groundwater and porewater exhibit different hydrochemical facies which may indicate sulfate
exceedances in these wells may not be due to the ash basin. Sulfate concentrations in
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monitoring wells screened within the bedrock flow layer exceeded the 2L Standard near the
compliance boundary north of ash basin Cell 2 at GWA-6BR and GWA-6BRU and near the
compliance boundary east of Cell 2 at GWA-2BR. Comparing the ionic composition of
groundwater samples from GWA-6BR, GWA-6BRU, and GWA-2BR to ash porewater
samples (see Section 10.7) indicates the groundwater and porewater exhibit different
hydrochemical facies which may indicate that the sulfate exceedances in these wells may not
be due to the ash basin.
• TDS concentrations in monitoring wells screened within the shallow flow layer exceeded the
2L Standard within the ash storage area at AS-1 S and near the compliance boundary north
of ash basin Cell 2 at GWA-6S. TDS concentrations in monitoring wells screened within the
deep flow layer exceeded the 2L Standard near the compliance boundary north of ash basin
Cell 2 at MW-10D. TDS concentrations in monitoring wells screened within the bedrock flow
layer exceeded the 2L Standard near the compliance boundary north of ash basin Cell 2 at
GWA-6BR and GWA-6BRU, and near the compliance boundary east of Cell 2 at GWA-2BR.
Locations of these TDS exceedances match locations where sulfate exceeded its 2L
standard.
• Thallium concentrations in monitoring wells screened within the shallow flow layer exceeded
the 2L Standard within the ash storage area at AS-1 S. There were no thallium concentrations
exceeding the 2L Standard in monitoring wells screened within the deep or bedrock flow
layers.
• Vanadium concentrations exceeded the IMAC in all wells screened within the shallow, deep,
and bedrock flow layers with the exception of MW-6S. The relative concentrations of
vanadium are generally higher in the deep then in the bedrock wells and shallow wells.
11.7 Groundwater / Surface Water Interaction
As discussed in Section 5.2, shallow and deep groundwater flow typically follows the
topographic gradient and shallow groundwater generally discharges to nearby surface water
bodies (i.e. streams).
Groundwater/surface water interaction is evident at the site based on the potentiometric surface
maps for the shallow flow layer, and to a lesser extent, for the deep flow layer in Figures 6-5 and
6-7. These figures illustrate a mounding effect where the ponded water within the ash basin is
driving groundwater flow towards the Yadkin River and toward the unnamed tributaries to the
Yadkin River located near the eastern and western extents of Buck. The ponded areas are
areas of recharge to the underlying flow layers as indicated by groundwater elevations near the
ponded areas generally correlating with the ponded water elevations.
Fluctuations in water level within the Yadkin River will not have a significant effect on
groundwater flow at Buck except at locations immediately adjacent to the river. The topographic
relief in the area is such that the typically minor fluctuations in river stage are small compared to
the elevations of the ash ponds. A survey performed in July 2015 indicated the stage within the
Yadkin River was at approximately elevation 620 feet while ponded water elevations within Cells
1, 2, and 3 of the ash basin were approximately 700, 682, and 673 feet, respectively.
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11.8 Estimated Seasonal High and Seasonal Low Groundwater
Elevations — Compliance and Voluntary Wells
Estimated Seasonal Low (ESL) and Estimated Seasonal High (ESH) groundwater elevations
were calculated using historical groundwater elevations for select compliance and voluntary
wells at the site. The calculated ESL and ESH depth to water (DTW) was performed statistically
by multiplying the standard deviation of the historical DTW measurements by a factor of 1.2
then adding to the mean DTW measurement. To obtain the site modification factors for ESL and
ESH conditions, the calculated ESL and ESH DTW in the historical site wells were compared to
the current groundwater levels on site and the difference was calculated. The difference
between ESH and ESL DTW and current conditions was then averaged for the representative
site wells to create a modification factor to add to current DTW. Compliance wells MW-8S, MW-
9S, MW-1OD, MW-11S, MW-12S and MW-13D were selected as the most representative
shallow wells for natural seasonal fluctuations at the site, as they are located away from the ash
basin and are, therefore, less likely to be influenced by the water level in the ash basin system.
Appendix H summarizes calculated ESH and ESL groundwater elevations for newly installed
groundwater monitoring wells.
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12.0 Screening -Level Risk Assessment
The prescribed goal of the human health and ecological screening level risk assessments is to
evaluate the analytical results from the COI sampling and analysis effort and using the various
criteria taken from applicable guidance, determine which of the COls may present an
unacceptable risk, in what media, and therefore, should be carried through for further evaluation
in a baseline human health or ecological risk assessment or other analysis, if required.
Contaminants of Potential Concern (COPCs) are those COls that have been identified as
having possible adverse effects on human or ecological receptors that may have exposure to
the COPCs at or near the site. The COPCs serve as the foundation for further evaluation of
potential risks to human and ecological receptors.
To support the CSA effort and inform corrective action decisions, a screening level evaluation of
potential risks to human health and the environment to identify preliminary, media -specific
COPCs has been performed in accordance with applicable federal and state guidance, including
the Guidelines for Performing Screening Level Ecological Risk Assessments within the North
Carolina Division of Waste Management (NCDENR, 2003). The criteria for identifying COPCs
vary by the type of receptor (human or ecological) and media, as shown in the comparison of
contaminant concentrations in various media to corresponding risk -based screening levels
presented in Tables 12-1 through 12-8.
In the human health and ecological screening level risk assessments, the maximum
concentrations detected for all COls, [or other appropriate data point (i.e., the analytical
reporting limit [RL]) in the 2015 sampling and analyses for coal ash detection and assessment
monitoring analytes were compared against established and conservative human health and
ecological screening toxicity reference values, likely to be protective for even the most sensitive
types of receptors.
These comparisons are used to determine which COls present a potentially unacceptable risk to
human and/or ecological receptors and may warrant further evaluation. Those COls determined
to pose a potential for adverse impacts are identified as preliminary COPCs.
Other factors that will be considered qualitatively in the evaluation of final COPCs that would be
incorporated into a baseline risk assessment include frequency of detection and a comparison
to background. Site- and media -specific risk -based remediation standards may be calculated,
pending additional sample collection, if and where additional sampling and site -specific
standards are deemed necessary.
12.1 Human Health Screening
12.1.1 Introduction
This screening level human health risk assessment has been prepared in accordance with
applicable NCDENR and USEPA guidance and the approved Work Plan.
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12.1.2 Conceptual Site Model
The Conceptual Site Model (CSM) is a dynamic tool for understanding site conditions and
potential exposure scenarios for human receptors that may be exposed to site -related
contamination. The CSM provides graphical representation of the following:
• A source and mechanism of chemical release;
• A retention or transport medium for COPCs;
• A point of contact between the human receptor and the medium; and
• A route of exposure to constituents for the potential human receptor at the contact point.
An exposure pathway is considered complete only if all four "source to receptor" components
are present. A CSM has been prepared illustrating potential exposure pathways from the source
area to possible receptors (see Figure 12-1). The information in the CSM has been used in
conjunction with the analytical data collected as part of the CSA to determine COPCs for the
site.
Potential receptors are defined as human populations that may be subject to contaminant
exposure. Both current and future land and water use conditions were considered when
determining exposure scenarios. Current and future land use of the Buck site and associated
ash basin and ash storage area is expected to remain predominantly industrial while
decommissioning of the coal-fired generating station is in progress (HDR 2014d). The BCCS
natural gas facility will remain in active use for the foreseeable future. Lands surrounding the
site include residential, undeveloped and recreational areas, as well as Yadkin River, which
supplies water to various municipalities.
The following potential receptors are identified in the CSM:
• Current/future on -site construction worker with potential exposure to groundwater in
trenches, surface and subsurface soil and surface water;
• Current/future on -site outdoor worker with potential exposure to surface soil and surface
water;
• Current/future adult and child off -site resident with potential exposure to surface soil and
groundwater; and
• Current/future on -site trespasser with potential exposure to surface soil, surface water
and sediment.
Other exposure pathways for all potential receptors were evaluated and it was determined that
they would not have a significant impact on the risk assessment (e.g., outdoor worker inhalation
of inorganics in surface water in open air). Other exposure scenarios will also serve as
surrogates that will provide information about the magnitude of these potential risks.
The following presents a description of each receptor and potentially complete exposure
pathway:
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12.1.2.1 Current/Future Construction Worker
It was assumed that construction activities during decommissioning and restoration of Buck
could take place on -site and that construction workers would potentially be exposed to COPCs
in various media during this timeframe. The potentially complete exposure pathways include
incidental ingestion, dermal contact and particulate inhalation exposure to surface and
subsurface soil. Construction workers in a trench with contact to groundwater may have
inhalation of metal COPCs with inhalation toxicity criteria and incidental ingestion of and dermal
contact (over limited parts of the body) with groundwater. Given the presence of the ash basin
and ash storage area, dermal contact and incidental ingestion exposure to surface water would
also be considered a potentially complete exposure pathway for this receptor.
12.1.2.2 Current/Future Outdoor Worker
Outdoor workers are assumed to be involved with non -intrusive activities (e.g., landscapers that
will maintain the site). This receptor reflects a longer timeframe and different exposure pathways
than that of construction workers. Outdoor workers are assumed to have incidental ingestion,
dermal contact and particulate inhalation exposure to surface soil as well as dermal contact and
incidental ingestion exposure to surface water (e.g., ash basins).
Exposure to COPCs in groundwater is not identified in the CSM because outdoor workers are
assumed not to ingest untreated water; any COPCs aerosols or fumes will dissipate in open air,
and there is limited opportunity for dermal contact. Construction worker exposure scenarios are
considered a conservative surrogate to estimate the potential risk from groundwater to outdoor
workers.
12.1.2.3 Current/Future Off -Site Resident (Adult/Child)
The potential for off -site residents to be exposed to COPCs in untreated groundwater is
included in the CSM, as approximately 170 private water supply wells and springs were
identified in Rowan County within a 0.5-mile radius of the ash basin compliance boundary south
of the Buck site, as described in Section 4.0 above and the 2014 Drinking Water Supply Well
and Receptor Survey and its Supplement (HDR 2014a and b) (Figure 4-1). These exposures
will consider all on and off -site monitoring well data, excluding the receptor survey data, which is
being handled independent of this risk analysis.
Exposure routes are to include ingestion of groundwater (not incidental, but potable use) as well
as dermal contact during bathing/showering and inhalation during bathing/showering for those
metals in groundwater with available inhalation -based toxicity criteria.
Residents are potentially exposed to contaminants in surface soil during non -intrusive outdoor
activities (e.g., lawn mowing); the potential exposure pathways include ingestion, dermal and
inhalation of soil particulates.
The Yadkin River is a public drinking water supply that is treated before consumption (Salisbury -
Rowan Utilities, 2015); therefore, residential exposure to COPCs in untreated surface water has
not been evaluated.
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12.1.2.4 Current/Future Trespasser (Adolescent/Adult)
Trespassers may come into direct contact with or incidentally ingest surface water and sediment
while on -site and near the Yadkin River during what is assumed to be predominantly
recreational activity. This will occur at different rates depending on the specific activity and
setting. The exposure parameters for this scenario will be determined and will incorporate all on -
and off -site data for these media.
Exposure routes are to include incidental ingestion, dermal contact and particulate inhalation of
surface soil, as well as incidental ingestion and dermal contact with surface water and sediment.
This receptor reflects greater exposure to surface water, sediment and soil COPCs compared to
potential exposures of similar potential receptors (e.g., off -site recreator).
12.1.3 Human Health Risk -Based Screening Levels
A comparison of contaminant concentrations in various media to corresponding risk -based
screening levels has been made and is presented in Tables 12-1 through 12-5. These include:
• Groundwater: USEPA tap water RSLs, NCDENR 2L Standards, and North Carolina
interim maximum allow concentration (IMAC) criteria
• Soil: USEPA industrial soil Regional Screening Levels (RSLs) at a target cancer risk of
1 E-06 and noncancer Hazard Quotient of 0.1
• Surface water: USEPA National Recommended Water Quality Criteria and NCDENR 2B
Standards, considering the surface water classification for local water bodies
• Sediment: USEPA residential soil RSLs
Table 12-1 presents the Comparison of Groundwater Sample Concentrations to USEPA Tap
water Regional Screening Levels, NCDENR 2L Standards and IMAC criteria; Table 12-2, the
Comparison of Soil Sample Concentrations to USEPA Residential and Industrial Soil Regional
Screening Levels; and Table 12-3, the Comparison of Sediment Sample Concentrations to
USEPA Residential Soil Regional Screening Levels.
Table 12-4 present a summary of the COls that were detected at concentrations exceeding their
relevant human health or other applicable criteria on a media -specific basis, in groundwater,
surface water, sediment, and soil.
Those COls exceeding relevant screening criteria are identified as COPCs for purposes of this
human health risk assessment.
• In groundwater, lead, titanium and zinc were eliminated as COPCs. With the exception
of sodium, which was retained because no screening value were available for
comparison, all other COls exceeded their respective screening value. See Table 12-1
for maximum concentrations detected, the detailed screening results, identification of
COPCs and contaminant categories.
• Arsenic, cobalt, iron and manganese were detected at concentrations exceeding the
industrial soil screening levels and are determined to be COPCs. Sodium was retained
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by default, because the RL for this analyte exceeded the screening value. See Table 12-
2 for the soil COI maximum concentrations, COPCs and contaminant category data.
Aluminum, arsenic, cobalt, iron, manganese and vanadium are determined to be COPCs
based on exceedances of screening values. Antimony and thallium are retained because
the RL was used as maximum detected value or the RL exceeded screening values;
sodium was retained because no comparison criteria were available. Sediment COPCs
and contaminant categories are presented in Table 12-3.
COls were not screened out as COPCs based on a comparison to background concentrations,
as USEPA recommends all COls exceeding risk -based screening levels be considered in a
baseline risk assessment (USEPA 2002). Statistical background concentrations have been
developed as Prediction Limits (PLs), calculated for each COI using groundwater data in site
background wells. PLs are a calculation of the upper limit of possible future values based on the
Statistical Analysis of Groundwater Monitoring Data at RCRA Facilities Unified Guidance
(USEPA, March 2009). If concentrations of COI detected exceed the PL, then the groundwater
concentrations are assumed to have increased above background levels. Site -specific
background concentrations will be considered in the uncertainty section of the baseline risk
assessment, if determined to be required.
12.1.4 Site -Specific Risk Based Remediation Standards
Based on the results of the comparison to risk -based screening levels, media -specific
remediation standards will be calculated in accordance with the Eligibility Requirements and
Procedures for Risk -Based Remediation of Industrial Sites Pursuant to North Carolina General
Statute 130A-310.65 to 310.77 should additional sample collection and site -specific standards
be deemed necessary.
12.1.5 NCDENR Receptor Well Investigation
Approximately 90 off -site private water supply wells and one public water supply well were
sampled and analyzed for constituents as part of the NCDENR well testing program, as
described in Section 4.0. At Buck, vanadium ranged from 1.63--97.86 pg/L in the wells sampled;
iron from 323-5720 fag/L; manganese, 80.5-108 pg/L; and zinc from 2090 to 2600 pg/L.
Vanadium, iron, lead, manganese and zinc concentrations exceeded applicable drinking water
standards. NCDENR recommended that 74 wells not be utilized for drinking water due to
presence of vanadium, hexavalent chromium, iron, manganese, sodium, sulfate, and/or cobalt
in one or more of these wells. All of the off -site private water supply wells are upgradient of the
ash basin.
12.1.6 Human Health Risk Screening Summary
A human health CSM was developed to identify potential pathways of exposure from COPC
source to receptor populations; including several possible exposure scenarios. Maximum
concentrations of COls were compared to media -specific screening levels; COls exceeding
screening levels and those having no screening levels or issues with RLs were retained as
COPCs, in accordance with guidance.
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As a result of the screening, three COls, lead, titanium and zinc were excluded as COPCs in
groundwater. Arsenic, cobalt, iron and manganese were retained as COPCs as a result of
exceeding their respective screening values; sodium was retained by default due to a lack of
screening criteria.
Six COls (i.e., aluminum, arsenic, cobalt, iron, manganese and vanadium) are determined to be
COPCs based on exceedances of their screening values in sediment.
12.2 Ecological Screening
12.2.1 Introduction
This screening -level ecological risk assessment (SLERA) has been prepared in accordance with
the Guidelines for Conducting a Screening Level Ecological Risk Assessments within the North
Carolina Division of Waste Management (NCDENR, 2003). An ecological CSM has been
developed for this site and is provided as Figure 12-2.
12.2.2 Ecological Setting
12.2.2.1 Site Summary
Refer to Section 2.0 for a description of the Buck site.
12.2.2.2 Regional Ecological Setting
The site is located in the Southern Outer Piedmont eco-region of North Carolina adjacent to
Yadkin River; this eco-region is bordered by the Northern Inner Piedmont and Carolina Slate
Belt eco-regions (Griffith et al. 2002).
12.2.2.3 Description of the Eco-Region and Expected Habitats
The region consists of irregular plains and low to moderate gradient streams with less
precipitation and elevation than the Inner Piedmont. The common rock types include gneiss,
schist and granite covered by deep saprolite and mostly red, clayey subsoil. Land cover
consists of mixed white oak forests, croplands and pastures, as well as pine plantations (Griffith
et al. 2002).
12.2.2.4 Watershed in which the Site is Located
The site is located in the Yadkin — Pee Dee River Basin watershed. The North Carolina portion
of the river basin encompasses approximately 7,200 miles.
12.2.2.5 Average Rainfall
The average annual precipitation for Salisbury has been 42.81 inches over the past 30 years.
The average for the State of North Carolina is 48.87 inches (Weather DB, 2015).
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12.2.2.6 Average Temperature
The average temperature for Salisbury is 59.55' F. The average winter temperature is 46.60 F.
The average spring temperature is 55' F. The average summer temperature is 75.5° F and
average fall temperature is 61.10 F (Weather DB, 2015).
12.2.2.7 Length of Growing Season
According to the North Carolina State University Cooperative Extension, the average growing
season for Rowan County is 201 days, with a standard deviation of 16 days.
12.2.2.8 Threatened and Endangered Species that use Habitats in the Eco-Region
A list of threatened and endangered species for Rowan County is provided in Table 12-8.
12.2.2.9 Site -Specific Ecological Setting
An ecological checklist and habitat figure has been completed for this site and is provided in
Appendix I.
The site is located on the Yadkin River (headwater of High Rock Lake) in Rowan County near
the town of Salisbury, North Carolina. The June 2015 AMEC Natural Resources Technical
Report identified ten potential jurisdictional wetland areas on the site measuring a total of
approximately 13.9 acres. No open water areas were identified. There were 11 potential
jurisdictional drainage features; nine intermittent and two perennial streams.
Portions of the Buck site adjacent to High Rock Lake are within the regulated 100-year
flood zone (AMEC, 2015).
Requests for information were submitted to several federal and state agencies, in accordance
with the North Carolina Guidelines for Performing Screening Level Ecological Risk
Assessments (NCDENR, 2003). A copy of the requests and responses are provided in
Appendix I and a summary of the information is provided, as follows.
North Carolina Department of Cultural Resources
In a letter dated June 23, 2015, the North Carolina Department of Cultural Resources indicated
that there are "no historic resources which would be affected by the project'.
North Carolina Natural Heritage Program
In a letter dated June 9, 2015, the North Carolina Natural Heritage Program (NCNHP) provided
information obtained from their database, both for the Buck site and within a one -mile radius of
the site (see Appendix 1).
According to the NCNHP database, High Rock Reservoir Wetlands, a Natural Area, is located
within the site. One Managed Area, North Carolina Agricultural Development and Farmland
Preservation Trust Fund Easement, is located within the site.
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Two Natural Areas, Leonard Road Slopes and Yadkin River/Grants Creek Forests, are within a
one -mile radius of the site. Managed Areas, Linwood Game Land and two North Carolina
Agriculture Development and Farmland Preservation Trust Fund Easements, are within a one -
mile radius of the site.
North Carolina Wildlife Resources Commission
In a letter dated June 19, 2015, the North Carolina Wildlife Resources Commission reported the
following:
• The site drains to High Rock Lake in the Yadkin -Pee Dee River basin.
• There are records for the federal species of concern and state special concern Eastern
small -footed bat (Myotis leibii) and the state threatened Eastern lampmussel (Lampsilis
radiata) near the site. In addition, there are historical records for the federal species of
concern and state special concern — vulnerable Carolina birdfoot-trefoil (Acmispon
helleri) near the site.
• Bald eagles nest and forage in the area.
• The site is breeding and roosting habitat for migratory waterfowl species including, but
not limited to, gadwall, mallard, green -winged teal, ring-necked duck, American black
duck, and wood duck. Other species that have been documented in the area, but not
necessarily on the site, include: hooded merganser, ruddy duck, canvasback, scaup,
bufflehead, and redhead. In addition, the Buck site is nesting habitat for Osprey and
there are records for colonial wading bird colonies (great blue heron and great blue
heron/great egret) on or adjacent to the site.
• The site is used by migratory waterfowl (see species list above).
• There is recreational fishing in High Rock Lake. Recreational species include: striped
bass, largemouth bass, channel catfish, white crappie, black crappie, bluegill, white
bass, and flathead catfish.
United States Department of Agriculture, National Forests in North Carolina
In an email dated May 28, 2015, it was reported that there are no Designated and Proposed
Federal Wilderness and Natural Areas, National Preserves and Forests, or Federal Land
Designated for the Protection of Natural Ecosystems with a half -mile of Buck .
United States Department of the Interior, National Park Service
In an email dated June 3, 2015, the United States Department of the Interior, National Park
Service indicated that "the NPS has not identified any resource concerns at this time".
12.2.2.10 On -site and Off -site Land Use
On -site land use is approximately 30% heavy industrial, 5% light industrial, 55% undisturbed,
and 10% water bodies and cleared areas. Land use within a one -mile radius of the site is 50%
undisturbed, 20% residential, 20% agricultural, and 10% waterbodies (including the Yadkin
River).
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12.2.2.11 Habitats within the Site Boundary
Based on HDR's July 8, 2015 site visit, the following habitats are present on the Buck site.
• 166 acres of Mixed Hardwoods
• 40 acres of Pine Plantation
• 37 acres of Bottomland Hardwoods
10 acres of Shrub/Scrub
126 acres of Open Fields
• Aquatic features including ash basins, streams, and wetlands
For a detailed description of habitats, refer to the Checklist for Ecological Assessments located
in Appendix I.
12.2.2.12 Description of Man-made Units that may Act as Habitat
A 171-acre ash basin system (i.e., three cells) is present on site and may act as man-made
habitat.
12.2.2.13 Site Layout and Topography
The natural topography at the Buck site ranges from an approximate high elevation of 740 feet
near the southwest edge of the property near Dukeville Road to an approximate low elevation of
620 feet at the interface with the Yadkin River on the northern extent of the site. Topography
generally slopes from a south to north direction with an elevation loss of approximately 120 feet
over an approximate distance of 1.1 miles. Surface water drainage generally follows site
topography and flows from the south to the north across the site except where natural drainage
patterns have been modified by the ash basin or other construction (HDR, 2014).
12.2.2.14Surface Water Runoff Pathways
Swales, drainage ditches, and groundwater seeps were observed during HDR's July 8, 2015
site visit. Unnamed drainage features are located near the western and eastern edges of the site
and generally flow south to the Yadkin River.
12.2.2.15Soil Types
Based on lithological data obtained from soil boring and well installation activities conducted by
HDR during ash basin closure assessment activities (HDR, 2014C), subsurface stratigraphy
consists of the following material types: fill, ash, residual soil, saprolite, alluvium, PWR, and
bedrock. In general, residual soil, saprolite, and PWR were encountered on most areas of the
Buck site. Ash was encountered within the ash basin and ash storage area, while alluvium was
restricted to areas adjacent to historical drainage features in the northwest portion of ash basin
Cell 1 and the northeast portion of Cell 3 (i.e., near the Cell 1 and Cell 3 dams). Bedrock was
encountered between 67 feet and 113 feet in several deep borings completed within ash basin
Cells 1, 2, and 3 (HDR, 2014).
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During AMEC's review of the National Resource Conservation Service (NRCS) Soil Survey
indicated the presence of a number of soil map units, including Cecil sandy loam (CcC), Cecil
sandy clay loam (CeB2 and CeC2), Chewacla (ChA), Enon fine sandy loam (EnB and EnC),
Hiwassee clay loam (HwB2 and HwC2), Mecklenburg clay loam (MeB2 and McC2), Pacolet
sandy loam (PaD), Pacolet sandy clay loam (PcC2), Poindexter-Mocksville complex (PxD),
loamy Udorthents (Ud), Vance sandy loam (VaB and VaC), Vance sandy clay loam (VnB2),
Wahee loam (WaA), and open water (W) (AMEC, 2015).
12.2.2.16Species Normally Expected to Use Site under Relatively Unaffected Conditions
Terrestrial communities occur in both natural and disturbed habitats in the study area; these
may support a diversity of wildlife species. Information on the species that would normally be
expected to use this and similar sites in the Piedmont eco-region under relatively unaffected
conditions was obtained from relevant literature, mainly the Biodiversity of the Southeastern
United States, Upland Terrestrial Communities (Wiley and Sons, 1993).
Mammal species that may be present include eastern cottontail (Sylvilagus floridanus), gray
squirrel (Sciurus carolinensis), various vole, rat and mice species, red (Vulpes vulpes) and gray
fox (Urocyon cinereoargenteus), raccoon (Procyon lotor), Virginia opossum (Didelphis
virginiana), and white-tailed deer (Odocoileus virginiana).
Avian species are the most diverse. Canopy dwellers include the great crested flycatcher
(Myiarchus crinitus), Carolina chickadee (Parus carolinensis), tufted titmouse (P. bicolor), white
breasted nuthatch (Sitta carolinensis), blue -gray gnatcatcher (Polioptila caerulea), red -eyed
vireo (Vireo olivaceus), yellow -throated vireo (V. flavifrons), various warblers and tanagers, and
American redstart (Setophaga ruticilla).
Subcanopy species include a variety of woodpeckers, eastern pewee (Contopus virens),
Acadian flycatcher (Empidonax virescens), American crow (Corvus brachyrhynchos), blue jay
(Cyanocitta cristata), and Carolina wren (Thryothorus ludovicianus).
Catbirds (Dumetella carolinensis), brown thrashers (Toxostoma rufum), and mockingbirds
(Mimus polyglottos) are found along adjacent brushy edges, fields, and thickets.
Understory species include wood thrush (Hylocichla mustelina), American robin (Turdus
migratorius), white -eyed vireo (Virea griseus), Kentucky warbler (Oporornis formosus), common
yellow -throat (Geothlypis trichas), and yellow breasted chat (Icteria virens). Predatory birds
include several hawk and owl species, and the turkey vulture (Cathartes aura).
Amphibians and reptiles that tend to be associated with the terrestrial -aquatic interface in
streams, rivers, and open waters may include certain turtles (e.g., the Striped Mud and Gulf
Coast Spiny Softshell turtles); and frogs, snakes, and amphibians such as the Three -lined
salamander. For a more detailed description, see Appendix I.
Streams of the southeastern piedmont support a range of aquatic benthic macroinvertebrate
groups including mayflies (Ephemeroptera), stoneflies (Plecoptera), caddisflies (Trichoptera),
water beetles (Coleoptera), dragonflies and damselflies (Odonata), dobsonflies and alderflies
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(Megaloptera), true flies (Diptera), worms (Oligochaeta), crayfish (Crustacea), and clams and
snails (Molluscs).
Streams, rivers, ponds, and reservoirs support populations of game fish that may include
redbreast sunfish (Lepomis auritus), bluegill (Lepomis macrochirus), warmouth (Lepomis
gulosus), and largemouth bass (Micropterus salmoides). The most widespread non -game fish
species are American eel (Anguilla rostrata), eastern silvery minnow (Hybognathus regius),
bluehead chub (Nocomis leptocephalus), golden shiner (Notemigonus crysoleucas), spottail
shiner (Notropis hudsonius), whitefin shiner (N. niveus), swallowtail shiner (N. procne), creek
chub (Semotilus atromaculatus), creek chubsucker (Erimyzon oblongus), silver redhourse
(Moxostoma anisurum), yellow bullhead (Ictalurus natalis), flat bullhead (I. platycephalus),
margined madtom (Noturus insignis), and tessellated darter (Etheostoma olmstedi).
12.2.2.17 Species of Special Concern
For a detailed list of species of special concern that may be present, see Table 12-8.
12.2.2.18 Nearby Critical and/or Sensitive Habitats
For a detailed description, see Section III.D of the Ecological Checklist provided in Appendix I.
12.2.3 Fate and Transport Mechanisms
Potential fate and transport mechanisms at/near Buck include erosion, seeps, stormwater runoff
and flow of surface water bodies. An Ecological CSM (Figure 12-2) has been prepared
illustrating potential exposure pathways from the source area to possible ecological receptors.
The information in the Ecological CSM has been used in conjunction with the analytical data
collected as part of the CSA to develop an understanding of the sources, pathways and media
of exposure as well as the receptors potentially impacted by site -related COPCs.
12.2.4 Comparison to Ecological Screening Levels
The sampling and analysis program completed as part of the Buck CSA investigation is
described earlier in this report. Media of primary concern for ecological receptors, i.e., surface
water, sediment and soil have been sampled extensively, in accordance with the NCDENR
approved Work Plan.
The results of the comparison of COI concentrations in various media to risk -based screening
levels are presented in the following tables:
• Table 12-5, a Comparison of Soil Sample Concentrations to USEPA Ecological Soil
Screening Levels and USEPA Region IV Recommended Ecological Screening Values;
• Table 12-6, the Comparison of Sediment Sample Concentrations to USEPA Region IV
Recommended Ecological Screening Values;
These tables include the COPCs' respective category 1-5 determination (as applicable) and as
described in Section 12.1.3 above.
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The potential for ecological risk was also estimated by calculating screening hazard quotients
(HQ) using the appropriate screening value of each contaminant and comparing that value to
the USEPA Region IV Ecological Screening Values. COls having a HQ greater than or equal to
1 are identified as COPCs.
Table 12-7 presents a summary of the COls that were detected at concentrations exceeding
their relevant ecological screening media -specific or other criteria. Those COls exceeding the
relevant criteria are identified as ecological COPCs for purposes of the SLERA.
Note that NCDENR SLERA guidance does not allow for exclusion of COls as COPCs based on
a comparison to background concentrations.
NCDENR guidance requires a determination of which contaminant category the COPCs fall into
as a result of the data comparison to screening levels and is also presented in the ecological
COPC tables (Tables 12-6 through 12-8). These include:
• Category 1 — Contaminants whose maximum detection exceeds the media specific
ecological screening value included in the COPC tables.
• Category 2 — Contaminants that generated a laboratory SQL that exceeds the USEPA
Region IV media -specific ecological screening value for that contaminant.
• Category 3 — Contaminants that have no USEPA Region IV ecological screening value,
but were detected above the laboratory SQLs.
• Category 4 — Contaminants that were not detected above the laboratory SQLs and have
no USEPA Region IV ecological screening value.
In soil, all COls except cadmium, lead and mercury, were determined to be COPCs. Aluminum,
barium, beryllium, boron, total chromium, cobalt, copper, iron, manganese, molybdenum, nickel,
selenium, vanadium and zinc were detected at concentrations exceeding their respective
ecological soil screening levels. The other COls were retained based on issues regarding their
respective RL exceeding the screening values or a lack of criteria for comparison. These have
been retained as COPCs by default. See Table 12-5 for detailed information, including the
maximum concentrations detected. For several COPCs, the exceedances are greater than one
order of magnitude above the screening levels; these include aluminum, boron, total chromium,
iron, and vanadium.
COPCs identified in sediment based on a comparison of maximum detected concentrations to
available criteria include total chromium, copper, nickel and zinc; aluminum, antimony, arsenic,
barium, beryllium, boron, cadmium, cobalt, iron, manganese, molybdenum, selenium, sodium,
strontium, thallium, and vanadium were retained due to issues related to their RL exceeding the
screening value or there being no screening value available. Lead and mercury have been
excluded as COPCs. Details on the COPC screening and contaminant category are provided in
Table 12-6.
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COls were not screened out as COPCs based on a comparison to background concentrations,
as NCDENR SLERA guidance does not allow for screening based on background. Site -specific
background concentrations, discussed above in Section 12.1.3, will be considered in the
uncertainty section of the baseline ecological risk assessment, if determined to be necessary.
12.2.5 Uncertainty and Data Gaps
There are uncertainties inherent in any environmental investigation and risk evaluation that
involve the natural heterogeneity of the media, nature, and extent of constituents in the
environment, due to their individual fate and transport characteristics, and varied, site -specific
conditions. These uncertainties are considered in developing the sampling and analysis plan,
data quality assurance processes, and understanding of the site.
These screening level assessments are designed to be very conservative in identifying potential
COPCs that would be carried forward into a baseline human health, and/or ecological risk
assessment. They include all on- and off -site analytical data, and use the maximum
concentration detected as the comparison point to applicable screening criteria. Also, no COls
were eliminated as COPCs based on background levels; this will be evaluated in the baseline
risk assessment, if they are required to be performed. These are highly unlikely to be the actual
exposure concentrations, given the natural attenuation, dilution, and distances to potential
receptors.
There is a high level of confidence that any constituent with potential to impact human health or
ecological receptors has been identified as a result of these assessments.
12.2.6 Scientific/Management Decision Point
If through the HQ analysis it is determined that COls have been detected at maximum
concentrations that exceed applicable screening criteria, that is an indication that additional
assessment of potential risks is warranted. This does not mean that impacts are in fact,
occurring; only that further data collection or evaluation should be considered.
This determination is known as the Scientific/Management Decision Point (SMDP) and the
conclusion reached must be one of the following:
• There is adequate information to conclude that the ecological risks are neglibible; or
• Site has inadequate data to complete the risk characterization. Data gaps need to be
filled prior to completion of the screening process; or
• The information indicates a potential for adverse ecological effects and a more thorough
assessment is warranted.
Given that several COPCs have been identified as having a HQ of greater than 1 in soil, surface
water and sediment, there is adequate information indicating a potential for adverse effects to
occur and further assessment may be warranted. The need for further evaluation should be
considered in light of the other ongoing or planned environmental impact studies for this site.
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12.2.7 Ecological Risk Screening Summary
Cadmium, lead and mercury are the only COls that have been excluded as COPCs in soil;
several COPCs exceed their respective screening criteria by one or more orders of magnitude.
Fewer COPCs have been identified in sediment and several of those are retained by default for
having no criteria or due to RL issues, not due to maximum concentrations actually exceeding
screening criteria. Impacts from limited ecological receptor groundwater exposure are minimal
and have not been evaluated. For Buck, identification of potential data gaps and overall
coordination of further ecological risk assessment efforts, specifically for surface water and
sediment impacts, should consider the other activities that are ongoing related to ash basin
closure activities to avoid duplication of effort.
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13.0 GROUNDWATER MODELING
13.0 Groundwater Modeling
Groundwater modeling will be performed and submitted in the CAP in accordance with
NCDENR's Conditional Approval letter. The groundwater modeling will consist of groundwater
flow and fate and transport modeling, performed with MODLFOW and MT3DMS, and batch
geochemical modeling, performed with PHREEQC. The following section presents an overview
of the fate and transport modeling, the batch geochemical modeling and the site geochemical
conceptual model.
The CAP will also present a discussion of the geochemical properties of the COls and how
these properties relate to the retention and mobility of these constituents.
13.1 Fate and Transport Groundwater Modeling
A three-dimensional groundwater flow and contaminant fate and transport model
(MODFLOW/MT3DMS Model) will be developed for the ash basin site. The objective of the
modeling will be to predict the following in support of the CAP:
• Predict concentrations of the COls at the compliance boundary or other locations of
interest over time,
• Estimate the groundwater flow and constituent loading to surface water discharge areas,
and
• Predict approximate groundwater elevations in the ash for the proposed corrective action
The model and model report will be developed in general accordance with the guidelines found
in the memorandum Groundwater Modeling Policy, NCDENR DWQ, May 31, 2007.
The groundwater model will be developed from the hydrogeologic conceptual model presented
in the CSA, from existing wells and boring information provided by Duke Energy, and from
information developed during the site investigation. The model will also be supplemented with
additional information developed by HDR from other Piedmont sites, as applicable. The site
conceptual model (SCM) is a conceptual interpretation of the processes and characteristics of a
site with respect to the groundwater flow, boundary conditions, and other hydrologic processes
at the site.
Although the site is anticipated in general to conform to the LeGrand conceptual groundwater
model, due to the configuration of the ash basin and the boundary conditions present at the site,
a three-dimensional groundwater model is warranted.
The groundwater modeling will be performed under the direction of Dr. William Langley, P.E.,
Department of Civil and Environmental Engineering, University of North Carolina Charlotte
(UNCC). Groundwater flow and constituent fate and transport will be modeled using Visual
MODFLOW 2011.1 (flow engine USGS MODFLOW 2005) and MT3DMS.
The modeling process, the development of the model, the development of the hydrostratigraphic
layers, the model extent (or domain), and the proposed model boundary conditions were
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described in Section 7.0 of the work plan. To date, no changes to the proposed model
development are warranted based on data collected during the site investigation.
The MUDMS model will use site specific Kd values developed from samples collected along
the major flow transects. The testing to develop the Kd terms is underway, but is not complete
at this time; therefore, the results of that testing will be presented in the CAP. The methods used
to develop the Kd terms was presented in Section 7.7.2 of the work plan.
13.2 Batch Geochemical Modeling
As described in the work plan, batch geochemical simulations using PHREEQC will be used to
estimate sensitivity of the proposed sorption constants used with MT3DMS and to assist in
understanding the mechanisms involved in attenuation of selected constituents. Geochemical
modeling using PHREEQC can be used to indicate the extent to which a COI is subject to
solubility constraints, a variable Kd, or other processes. PHREEQC can also identify postulated
solid phases calculation of their respective saturation indices. The specific locations where the
batch geochemical modeling will be performed will be determined after the development of the
Kd terms and a review of the site data.
13.3 Geochemical Site Conceptual Site Model
SCMs are developed to be a representation of what is known or suspected about contamination
sources, release mechanisms, transport, and fate of those contaminants.4 An SCM can be a
written and/or graphic presentation of site conditions to reflect the current understanding of the
site, identify data gaps, and be updated as new information is collected throughout the project.
SCMs can be utilized to develop understanding of the different aspects of site conditions, such
as a hydrogeologic conceptual site model, to help understand the site hydrogeologic condition
affecting groundwater. SCMs can also be used in a risk assessment to understand contaminant
migration and pathways to receptors.
On June 25, 2015, NCDENR made the following request:
Since speciation of groundwater and surface water samples is a critical component of
both the site assessments and corrective action, the Division expects a geochemical site
conceptual site model (CSM) developed as a subsection in the Comprehensive Site
Assessment (CSA) Reports. The geochemical CSM should provide a summary of the
geochemical interactions between the solution and solid phases along the groundwater
flowpath that impact the mobility of metal constituents. At a minimum, the geochemical
CSM will describe the adsorption/desorption and mineral precipitation/dissolution
processes that are believed to impact dissolved concentrations along the aquifer
flowpaths away from the ash basin sources. The model descriptions should include the
data upon which the conceptual model is based and any calculations (such as mineral
saturation indices) that are made to develop the site -specific model.
4 EPA MNA Volume 1
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Metal speciation analyses cover a broad aspect of metals' geochemistry, including
solution complexation with other dissolved species and specific association with aquifer
solids, such as a metal adsorbed onto HFO or precipitated as a sulfate mineral. A
comprehensive speciation analysis that requires a relatively complete groundwater
analysis is expected that includes use of an ion speciation computer code (such as
PHREEQC) capable of calculating solution complexes, surface complexation onto HFO,
and mineral saturation indices. This type of speciation calculation is necessary for the
development of a geochemical SCM and understanding metal mobility in an aquifer.
In previous correspondence, NCDENR agreed that the proposed geochemical modeling
described in the Work Plan, to be performed using PHREEQC, will be included in the CAP.
Specifically, the model descriptions and calculations, such as mineral saturation indices, will be
provided in the CAP. This approach will allow completion of the testing to develop the site -
specific Kd terms and site mineralogy, and will allow the geochemical modeling to be
coordinated with the groundwater flow and transport model.
Elements of the geochemical site conceptual site model (GSCM) described below will be
incorporated into the fate and transport and the geochemical modeling performed for the CAP.
The GSCM will be updated as additional data and information associated with contaminants,
site conditions, or processes such as migration of contaminants is developed. The GSCM will
be useful in understanding the transport and attenuation factors that affect the mobility of
contaminants at the site and the long-term capacity of the site for attenuation and stability of
immobilized contaminants.
The GSCM will describe the geochemical aspects of the site sources that influence contaminant
transport. Site sources at Buck consist of the ash basin and ash storage area. These source
areas are subject to different processes that generate leachate migrating into the underlying soil
layers and into the groundwater. For example, the ash storage area would generate leachate as
a result of infiltration of precipitation, while the ash basin would generate leachate based on the
pond elevation in the basin. General factors affecting the geochemistry of the site are as follows:
Factors Affecting Ash Formation (Primary Source):
• Chemical and mineralogical composition of coal
• Thermodynamics of coal combustion process
Factors Affecting Leaching in the Ash Basins (Primary Source Release Mechanism):
• Chemical composition of ash
• Mineral phase of ash
• Physical characteristics of ash
• Inflow of water into/out of basin
• Period of time ash has been in basin
• Geochemical conditions in ash basin
• Precipitation -dissolution reactions
• Sorptive properties of materials in ash
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Factors Affecting Leaching in the Ash Storage Area (Primary Source Release
Mechanism):
• Chemical composition of ash in storage area
• Mineral phase of ash in storage area
• Physical characteristics of ash in storage area
• Inflow of precipitation in to ash storage area
• Period of time ash has been in storage
• Geochemical conditions in ash storage area
• Precipitation -dissolution reactions
• Sorptive properties of materials in ash
Factors Affecting Sorption and Precipitation of Constituents onto Soil/Aquifer Materials
Beneath Ash (Secondary Source Release Mechanism):
• Chemical composition of soil
• Physical composition of soil
• Rate of infiltration/percolation of porewater
• Chemical composition of leachate infiltrating into soil
• Sorption capacity of soil
• Geochemistry of groundwater flowing beneath unit
Factors Affecting Desorption and Dissolution of Constituents From Soil/Aquifer Materials
Beneath Ash (Secondary Source Release Mechanism):
• Chemical composition of soil
• Physical composition of soil
• Rate of infiltration/percolation of porewater
• Attenuation capacity of soil
• Chemical composition of leachate or precipitation infiltrating into soil
• Geochemistry of groundwater flowing beneath unit
The results of the Kd testing, the results from the site mineralogy testing, and the geochemical
modeling developed in the CAP will be used to refine the GSCM.
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14.0 DATA GAPS — CONCEPTUAL SITE MODEL UNCERTAINTIES
14.0 Data Gaps — SCM Uncertainties
14.1 Data Gaps
Through completion of groundwater assessment field activities and evaluation of data collected
during those activities, Duke Energy has identified data gaps that will require further evaluation
to refine the SCM. The data gaps have been separated into three groups: 1) data gaps resulting
from temporal constraints, 2) data gaps resulting from evaluation of data collected during the
CSA, and 3) data gaps resulting from other sources.
14.1.1 Data Gaps Resulting from Temporal Constraints
Data gaps identified in this category are generally present due to insufficient time to collect,
analyze, or evaluate data collected during the CSA activities. It is expected that the majority of
these data gaps will be remedied in a CSA supplement to be submitted to NCDENR following
completion of the second comprehensive groundwater sampling event.
• Mineralogical Characterization of Soil and Rock: a total of 16 soil, three TZ, and nine
bedrock samples were submitted to three third -party mineralogical testing laboratories
for analysis of soil and rock composition. As of the date of this report, Duke Energy has
not received all of the results of this testing; however, results should be available for
inclusion in the CSA Supplement. This data is important with regard to evaluating some
of the COI concentrations measured above 2L Standards or IMACs and above the
background well concentrations. These measured constituent concentrations were
identified in cross- or downgradient wells north and west of the source.
• Dry Sampling Locations: Due to dry conditions at the time of the initial sampling event,
several proposed sampling locations could not be sampled. These locations included
NCDENR seep locations (BS SWO01AA S001, BS SWO03AA S001, BSSW074SO01,
and BSSW074SO01), two other seep locations noted above (Wet Area Near Pump
House and Terracotta Pipe #2), and surface water locations along an unnamed tributary
to the Yadkin river located on the east side of the Buck site (SW-1 and SW-2). Two
groundwater monitoring wells were also dry at the time of sampling (BG-1 BR and AB-
5D). Another attempt to sample these locations will be made and results will be provided
in the CSA Supplement.
14.1.2 Data Gaps Resulting from Review of Data Obtained During CSA Activities
A shallow groundwater monitoring well in the nest of GWA-2BRU and GWA-2BR would
assist with the groundwater flow direction determination at this location. Two additional
monitoring well nests, consisting of a shallow and deep well each, located nortwest and
southwest of GWA-2BRU/BR would assist in refining groundwater flow direction in this
area and provide information regarding constituent concentrations between Cell 2 and
the Cell 3 ponds.
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• The bedrock background monitoring well BG-1 BR could not be sampled due to
insufficient water in the well during the sampling event. A replacement bedrock
background well in this location may be warranted if BG-1 BR is not a viable well.
• Groundwater samples were not collected from all of the onsite voluntary wells or existing
monitoring wells that were installed during the site closure investigation. During
subsequent sampling events, groundwater elevations will be measured and groundwater
samples will be collected from these wells in conjunction with the newly installed
assessment monitoring wells.
• Obtain soil samples located outside of the ash basin for SPLP analysis to compare
results against SPLP analysis of ash.
• Perform minerology analysis of soil and rock samples in wells where COls are present
above 2L Standards or IMACs to determine if constituents occur naturally.
14.1.3 Data Gaps Resulting from Other Sources
Sampling of Off -Site Seeps: The Work Plan included obtaining a surface water sample
(S-1 A) and samples at two seep locations (S-1 B and S-1 C) associated with an off -site
pond located near the eastern extent of Duke Energy's property boundary. Duke Energy
was not able to obtain permission from the property owner to gather these samples.
Permission to obtain these samples should be pursued for future sampling events.
14.2 Site Heterogeneities
Heterogeneities, with regard to groundwater flow, were not identified during completion of the
CSA. In general, groundwater within the shallow flow layer, TZ material, and fractured bedrock
flows toward small streams/drainage features located near the western and eastern extents of
Buck or north toward the Yadkin River.
Heterogeneities, with regard to COI concentrations, were not identified during completion of this
CSA. However, heterogeneities may be identified following completion of the groundwater
model for Buck.
14.3 Impact of Data Gaps and Site Heterogeneities
Certain data gaps can be addressed with additional groundwater and surface water sampling at
existing wells. As discussed in Section 15, the second comprehensive groundwater sampling
event is planned for August/September 2015. A plan for interim groundwater sampling between
submittal of the CSA and implementation of the anticipated CAP is proposed in Section 16 and
will further supplement the existing data.
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15.0 PLANNED SAMPLING FOR CSA SUPPLEMENT
15.0 Planned Sampling for CSA Supplement
The specifics of a second comprehensive sampling event at the Buck site are currently under
discussion between NCDENR and Duke Energy. The second sampling event will be conducted
to:
• Supplement data obtained during the initial sampling event;
• Evaluate seasonal variation in groundwater results; and
• Potentially collect additional samples for chemical speciation of arsenic, chromium, iron,
manganese and selenium, although such additional samples are not currently needed
for CAP development or further risk assessment.
15.1 Sampling Plan for Inorganic Constituents
All samples collected will be analyzed for total inorganic compounds. Samples with
exceedances of 2L Standards or IMACs during the initial sampling event will also be analyzed
for dissolved -fraction inorganics. The scope of the second event sampling is anticipated to be
the following:
• Collection of second set of data for all new site assessment wells, seeps and surface
water for CSA Work Plan parameters (including total and dissolved metals using 0.45
pm filters);
• Locations that were previously dry will be re-evaluated and sampled if sufficient water is
present to do so; and
• Collection of dissolved metals data using 0.1 pm filters from the flow transect wells
selected for geochemical modeling.
15.2 Sampling Plan for Speciation Constituents
Duke Energy and NCDENR are currently conducting discussions concerning the specifics of the
requirements for sampling associated with speciation. A summary of the proposed sampling
program for the second comprehensive sampling event is included on Table 15-1.
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16.0 INTERIM GROUNDWATER MONITORING PLAN
16.0Interim Groundwater Monitoring Plan
CAMA requires a schedule for continued / interim groundwater monitoring. In addition, Duke
Energy is required to implement closure and remediation of the Buck ash basin, which is not yet
defined in CAMA. However, CAMA does require Duke Energy to submit a proposed closure
plan such that NCDENR can prioritize site closure based on risk classifications. As such, Duke
Energy plans to conduct interim groundwater monitoring at select wells identified in Table 15-1
to bridge the gap between completion of CSA activities and implementation of the proposed
CAP.
16.1 Sampling Frequency
Interim groundwater sampling is planned to occur two additional times during 2015/early 2016
(timing will be such that the samples are not auto -correlated), then quarterly until the CAP is
approved by NCDENR and implemented by Duke Energy. This sampling frequency will allow for
evaluation of seasonal fluctuations in COI concentrations, as well as provide additional data for
statistical analysis of site -specific background concentrations.
16.2 Constituent and Parameter List
The proposed constituents and parameters for analysis remain the same and are presented in
Table 7-3
16.3 Proposed Interim Sampling Locations
The proposed sampling locations are to remain the same and are shown on Figure 6-2.
16.4 Proposed Interim Background Wells
The proposed background wells are BG-1 S/D/BR, BG-2S/D, BG-3S/BRU, and MW-6S/D. Note
that outside of this Interim Groundwater Monitoring Plan, background wells are planned to be
sampled a total of four times in 2016.
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17.0Discussion
17.1 Summary of Completed and Ongoing Work
To date, the following activities have been completed in support of this CSA:
• Installation of 64 groundwater monitoring wells within the ash basin and ash storage
area, beyond the waste boundary, and in background locations;
• Completion of topographic and well/boring location surveys;
• Collection of ash samples from borings completed within the waste boundary and
analysis for total inorganics, TOC, anions/cations, SPLP, and physical properties;
• Collection of soil samples from borings completed within the waste boundary, beyond
the waste boundary, and background locations and analysis for total inorganics, TOC,
anions/cations, and physical properties;
• Collection of PWR and bedrock samples from borings completed within the waste
boundary, beyond the waste boundary, and background locations and analysis for total
inorganics, TOC, and anions/cations;
• Collection of soil samples for analysis of chemistry and mineralogy;
• Collection of rock samples for chemical analysis;
• Collection of rock samples for petrographic analysis (thin -sections);
• Performance of in -situ horizontal (open hole) and vertical (flush bottom) permeability
tests;
• Completion of packer tests in 6 bedrock borings;
• Completion of rising- and falling -head slug tests in 61 newly installed monitoring wells;
• Collection of groundwater samples from 78 newly installed, compliance, voluntary, and
previously installed monitoring wells, and analysis of samples for total and dissolved
inorganics, and anions/cations;
• Speciation of groundwater samples for arsenic, chromium, iron, manganese, and
selenium in groundwater samples collected from 46 monitoring wells installed along
anticipated groundwater flow transects;
• Collection of 7 surface water samples, 13 groundwater seep samples, and 14 sediment
samples, and analysis for total inorganics and anions/cations;
• Speciation of 21 groundwater seep sample for arsenic, chromium, iron, manganese and
selenium;
• Evaluation of solid and aqueous matrix laboratory data;
• Completion of an updated Receptor Survey; and
• Completion of fracture trace analysis; and
• Preparation of this CSA Report.
The following activities are on -going (as described in more detail in Section 14.1.1) and will be
provided to NCDENR in the CSA Supplement:
Analysis of soil samples for chemistry and mineralogy and rock samples for chemistry
and petrography;
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• Evaluation of the need for additional groundwater monitoring wells in the vicinity of the
GWA-2 monitoring well cluster to better define groundwater flow and the horizontal and
vertical extent of COls in the area.
• Additional speciation testing, if necessary, to support groundwater modeling activities;
and
17.2 Nature and Extent of Contamination
Soil and groundwater beneath the ash basin and ash storage area have been impacted by ash
handling and storage at Buck as shown on Figure ES-1. Concentrations of several COls
exceeded their respective 2L Standards or IMACs in groundwater beyond the compliance
boundary as shown on this figure. Samples obtained from on -site seeps also exhibit
concentrations of Cols exceeding their respective 2L Standards or IMACs.
As noted on Figure 10-9, exceedances of the 2L Standards and IMACs were observed in nearly
all monitoring wells across the site, including in monitoring wells located at the outermost extent
of the monitoring well system. Many of these COls were also identified in the background wells
and are not related to the ash basin or ash storage area. Preliminary review of these
exceedances indicates, in most cases, the exceedances observed at the outermost extent of
the monitoring well system are related to background water quality, naturally occurring
conditions, and/or sampling conditions. However, in areas downgradient of the source,
particularly north of the waste boundary, measured COI concentrations exceeded the 2L
Standards or IMACs and were higher than concentrations in background wells. Boron was also
measured outside of the compliance boundary on the north side of the site. Since
measurements of coal ash indicator COls for upgradient and side -gradient wells were similar to,
or below the measured ranges or concentrations in the background wells, there does not appear
to be coal ash related contamination south, east or west of the compliance boundary. A second
round of sampling will be performed at all locations sampled during the CSA. The results from
the CSA sampling, the second round of sampling, and the site -specific background
concentrations will be used to further define the source of these observed exceedances at the
site. The results of this evaluation will be presented in the CSA supplement.
17.2.1 Groundwater and Seep Contamination
COls identified in the source and above background and 2L Standards / IMACs were measured
in wells predominately downgradient of the sources. Some of these constituent levels were
measured in areas east and west of the source; however, most of these measurements were
made north of the source. With the flow direction being predominately south to north, with a
western component, the source does not appear to be impacting COI concentrations toward off -
site receptors immediately south and east of the of the Buck site; however, additional water
level information would be beneficial to better characterize the potentiometric surfaces in the
region southeast of GWA-2S/BR.
Seep sampling results at the Buck site have identified nine Cols in the seep water: antimony,
arsenic, boron, chromium, cobalt, iron, manganese, thallium, and vanadium. Comparing COI
concentrations in the seep water to the maximum COI concentrations encountered in
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groundwater sampled from the background wells indicates seven seep locations (BSWW002
S001, Terracotta Pipe #1, Culvert Discharge, S-2, S-3, S-5, and S-9) where at least one seep
COI concentration exceeded the maximum background groundwater COI concentration. Almost
all of the iron exceedances within the seep samples (9 of 10) occurred within unfiltered samples
indicating the source of the iron within the seep water is primarily suspended solids. Six COls
identified in the seep water (antimony, arsenic, boron, chromium, lead and thallium) occur at
concentrations exceeding the applicable groundwater standard at only one or two locations
each.
17.2.2 Soil, Rock, and Sediment Contamination
Soil samples were obtained from 29 separate drilling locations during CSA drilling within the
Buck site (including locations beneath the ash basin and ash storage area). For purposes of
this discussion, each drilling location is considered to include all borings drilled at the location
(i.e., all S, D, and BRU well borings). Within soil samples obtained from these locations, there
are eight COls identified in the soil: arsenic (5 locations), barium (1 location), boron (4
locations), cobalt (29 locations), iron (29 locations), manganese (29 locations), selenium (5
locations), and vanadium (29 locations). With the exception of barium, all of these COls appear
within one or more of the background well locations at concentrations exceeding the applicable
groundwater standard. The COI concentrations observed in the soil from the various locations
within the Buck site generally bracket the concentrations observed within soil samples from the
background locations or within a reasonable proximity of the bracketed background
concentrations.
Rock samples (including PWR samples) were obtained from ten separate drilling locations
during CSA drilling within the site (including locations beneath the ash basin and ash storage
area). For purposes of this discussion, each drilling location is considered to include all borings
drilled at the location (i.e., all S, D, and BRU well borings). Within rock samples obtained from
these locations, there are five COls identified in rock: arsenic (1 location), cobalt (8 locations),
iron (10 locations), manganese (9 locations), and vanadium (8 locations). With the exception of
arsenic, all of these Cols appear within the background location where rock was obtained (BG-
2) at concentrations exceeding the applicable groundwater standard.
Sediment samples were obtained from 14 seep locations at the Buck site. Within the sediment
samples, there are seven COls identified as constituents in sediment: arsenic (4 locations),
boron (1 location), cobalt (14 locations), Iron (14 locations), manganese (13 locations), selenium
(1 location), and vanadium (14 locations). A background sediment location (SW-2) was not
obtained due to dry conditions at the time of sampling; therefore a comparison of these results
with background conditions is not possible at this time. Such a comparison may be possible
after completion of the second comprehensive sampling event and will be included in the CSA
supplement.
17.3 Maximum Contaminant Concentrations
The maximum contaminant concentrations reported in groundwater, ash porewater, seep water,
and ash basin water samples collected during the CSA are listed below.
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Maximum Contaminant Concentrations for COls in groundwater are shown below:
• Antimony: 19.3 pg/L (GWA-2BR)
• Arsenic: 14.9 pg/L (AB-4BR)
• Barium: 830 pg/L (GWA-2BR)
• Boron: 3000 pg/L (AS-1 S)
• Chromium: 65.4 pg/L (GWA-7S)
• Cobalt: 356 pg/L (AS-1 S)
• Iron: 27,900 pg/L (AB-9S)
• Manganese: pg/L 4,100 ug/L (AS-1S)
• Nickel: 107 pg/L (AS-1S)
• Selenium: 30.3 pg/L (AB-4BR)
• Sulfate: 703,000 pg/L (AS-1S)
• Thallium 0.24 pg/L (AS-1 S)
• TDS: 1,040,000 pg/L (GWA-6BR)
• Vanadium 67.9 pg/L (GWA-11S)
Maximum Contaminant Concentrations for COls in porewater are shown below:
• Antimony: 24.4 pg/L (AB-2S)
• Arsenic: 1,350 pg/L (AB-2SL)
• Barium: 720 pg/L (AB-2SL)
• Boron: 6,500 pg/L (AB-4SL)
• Cobalt: 14.2 pg/L (AB-4S)
• Iron: 14,400 pg/L (AB-5SL)
• Manganese: 3,900 pg/L (AB-5SL)
• Thallium 0.67 pg/L (AB-8S)
• TDS: 565,000 pg/L (AB-2S)
• Vanadium: 347 pg/L (AB-2S)
Maximum Contaminant Concentrations for COls in seep water are shown below:
• Antimony: 2 pg/L (BSWW002 S001)
• Arsenic: 50 pg/L (BSWW002 S001)
• Boron: 1,000 pg/L (Terracotta Pipe #1)
• Chromium: 34.7 pg/L (Culvert Discharge)
• Cobalt: 1,050 pg/L (Culvert Discharge)
• Iron: 34,900 pg/L (S-2)
• Lead 21.9 pg/L (Culvert Discharge)
• Manganese: 6,300 pg/L (S-1)
• Thallium: 1.1 pg/L (Culvert Discharge)
• Vanadium: 174 pg/L (Culvert Discharge)
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Maximum Contaminant Concentrations for COls in ash basin surface water are shown below:
• Aluminum: 13,000 pg/L (SW-AB2)
• Antimony: 5.7 fag/L (SW-AB3)
• Arsenic: 71.3 fag/L (SW-AB4)
• Cadmium: 0.37 fag/L (SW-AB4)
• Chromium: 11.3 fag/L (SW-AB4)
• Cobalt: 23.9 fag/L (SW-AB2)
• Copper: 32.4 fag/L (SW-AB2)
• Iron: 35,000 fag/L (SW-AB4)
• Lead: 12.7 fag/L (SW-AB2, SW-AB4)
• Manganese: 640 fag/L (SW-AB4)
• Thallium: 0.45 fag/L (SW-AB2)
• Vanadium: 65.8 fag/L (SW-AB4)
• Zinc: 50 fag/L (SW-AB4)
• TDS: 560,000 fag/L (SW-AB3)
17.4 Contaminant Migration and Potentially Affected Receptors
Groundwater at the Buck site generally flows from south to north toward to the Yadkin River with
components of flow to the east and west toward unnamed tributaries to the Yadkin River located
near the eastern and western extents of the site.
A comparison of COls within samples of seep water to the maximum Cols in groundwater
samples obtained from background wells indicates eight seep locations where at least one COI
exceeded the maximum background groundwater COI concentration. The seep COls that
exceeded background groundwater COls include arsenic, boron, chromium, cobalt, iron, lead,
manganese, and vanadium. These seeps drain to either the unnamed tributaries to the Yadkin
River located near the eastern and western extents of the Buck site or directly to the Yadkin
River near the base of the ash basin Cell 2/3 dam. Based on this information, contaminated
groundwater is migrating to these surface water features.
A comparison of COls within samples of groundwater obtained from monitoring wells installed
near the ash basin compliance boundary to the maximum Cols in groundwater samples
obtained from background wells indicates 13 well locations where at least one COI exceeded
the maximum background COI concentration. For purposes of this discussion, each well
location is considered to include all borings drilled at the location (i.e., all S, D, and BRIJ well
borings). These well locations include MW-3, MW-10, MW-11, GWA-1, GWA-2, GWA-3, GWA-
4, GWA-5, GWA-6, GWA-7, GWA-9, and GWA-11. Based on this information, groundwater
impacted by the ash basin and ash storage area is migrating downgradient beyond the
compliance boundary.
The human health and ecological CSMs, provided as Figures 12-1 and 12-2 illustrate the
potentially affected receptors; these will be reviewed and revised as necessary based on
information indicated above.
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18.0 CONCLUSIONS
18.0 Conclusions
18.1 Source and Cause of Contamination
The CSA found that the source and cause of impacts (as shown on Figure ES-1) for certain
parameters in some areas of the site is the coal ash contained in the ash basin and ash storage
area. The cause of this contamination, shown in the referenced figure, is leaching of
constituents from the coal ash into the underlying soil and groundwater and subsequent
transport of the groundwater downgradient from the ash basin. However, some groundwater,
surface water and soil standards were also exceeded due to naturally occurring elements found
in the subsurface.
18.2 Imminent Hazards to Public Health and Safety and Actions
Taken to Mitigate them in Accordance to 15A NCAC 02L
.0106(f)
15A NCAC 02L .0106(g)(2) requires the site assessment to identify any imminent hazards to
public health and safety and the actions taken to mitigate them in accordance with Paragraph (f)
of .0106(g). The CSA found no imminent hazards to public health and safety; therefore, no
actions to mitigate imminent hazards are required. However, corrective actions at the Buck site
are required to address soil and groundwater contamination shown on Figure ES-1. These will
be addressed as part of the CAP.
18.3 Receptors and Significant Exposure Pathways
The requirement contained in the NORR and the CAMA concerning receptors was completed
with the results provided in Section 4.0. A screening level human health risk assessment and
screening level ecological risk assessment was performed with the results provided in Section
12.0. The identified receptors and significant exposure pathways are identified in the human
health and ecological CSMs (Figures 12-1 and 12-2).
18.4 Horizontal and Vertical Extent of Soil and Groundwater
Contamination and Significant Factors Affecting
Contaminant Transport
The CSA identified the horizontal and vertical extent of groundwater contamination within the
compliance boundary (as shown on Figure ES-1), and found that the source and cause of the
groundwater exceedances within that boundary is a result of both natural conditions and the
coal ash contained in the ash basin and ash storage area. In general, COls exceeding 2L
Standards or IMACs on the northern side of the waste boundary are judged to be highly
influenced by the source. Some of these exceedances were measured outside the compliance
boundary, although within the Duke Energy property boundary.
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18.0 CONCLUSIONS
Background monitoring wells contain naturally occurring metals and other constituents at
concentrations that exceeded their respective 2L Standards or IMACs. Examples of naturally
occurring constituents include antimony, cobalt, iron, manganese, and vanadium. Some of these
naturally occurring constituents were also detected in newly installed background monitoring
well groundwater samples at concentrations greater than 2L Standards or IMACs.
The horizontal and vertical extent of groundwater impacts above 2L Standards or IMACs is
shown, with exception of the areas associated with the data gaps identified in Section 14.1 on
Figures 10-10 through 10-51. Groundwater contamination is considered to be present where the
analytical results were greater than the site background concentrations and in excess of the 2L
Standards or IMACs. The assessment found COI groundwater concentrations above
background concentrations for antimony, arsenic, barium, boron, chromium, cobalt, iron,
manganese, nickel, selenium, thallium, vanadium, sulfate, and TDS. The approximate extent of
groundwater contamination is shown on these figures and is generally limited to an area within
the ash basin compliance boundary and the area north of the compliance boundary near the
Yadkin River (within the Duke Energy property boundary). Exceedances measured south, east,
and west of the waste boundary are judged to be predominately related to natural conditions,
although some source related exceedances were identified. All source related exceedances are
judged to be within the compliance boundary in these areas; however, some data gaps were
identified as discussed in Section 17.
The CSA found that the primary direction of flow and mobile contaminant transport is
predominately to the north toward the Yadkin River and not towards other off -site receptors. No
information gathered as part of this CSA suggests that water supply wells or springs within the
0.5-mile radius of the compliance boundary are impacted by the source.
This CSA also identified the horizontal and vertical extent of soil contamination as shown on
Figures 8-1 through 8-4. Soil contamination is considered to be present where analytical results
for COls were in excess of the maximum site soil background concentrations and in excess of
the most restrictive PSRG for each COI. The approximate contaminated soil extent is shown on
these figures. The assessment found the soil contaminants in excess of the maximum
background soil COI concentrations are arsenic, barium, boron, and iron.
The significant factors affecting contaminant transport are those factors that determine how the
contaminant reacts with the soil/rock matrix, resulting in retention by the soil/rock matrix and
removal of the contaminant from groundwater. The interaction between the contaminant and the
retention by soils are affected by the chemical and physical characteristics of the soil, the
geochemical conditions present in the matrix (if present), the matrix materials, and the chemical
characteristics of the contaminant. Migration of each contaminant is related to the groundwater
flow direction, the groundwater flow velocity, and the rate at which a particular contaminant
reacts with materials in the respective soil/rock matrix. The data indicates that geologic
conditions present beneath the ash basin impedes the vertical migration of contaminants.
The two primary mechanisms that immobilize metals (iron and manganese) and semi -metals
(arsenic, boron, and selenium) and prevent their movement in groundwater are sorption and
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18.0 CONCLUSIONS
precipitation (Ref NCDENR). The major attenuation mechanism for sulfate, a non-metal, is
sorption (EPRI). In these processes, the contaminant is in effect removed from groundwater and
partitions onto the surface of the soil/rock matrix (adsorption) or precipitates into a solid phase,
in both cases, removing the contaminant from groundwater.
A number of factors specific to the constituent and to site conditions are involved in determining
which of these mechanisms occur and how much of the contaminant partitions out of the
groundwater.
Sections 7.0, 8.0, 9.0, and 10.0 present the results of testing performed to evaluate the
chemical, physical, and mineralogical characteristics of the soil and aquifer materials and the
site groundwater. As described above, the determination of the mechanism and the amount of
the contaminant removed from the groundwater depends on a number of site specific factors.
The adsorptive capacity of the site soils and aquifer materials to the specific groundwater
contaminants is evaluated by development of site specific partition coefficient Kd terms, as
described in Section 13.0. The Kd testing provides site specific values for the ability and
capacity of site soils to remove contaminants from groundwater and will assist in understanding
the mechanisms affecting contaminant transport at the site. The Kd tests and the associated
groundwater modeling also allow for evaluation of the long-term contaminant loading and the
capacity of the site soil and aquifer material to attenuate this loading. The results of this testing,
the groundwater modeling, and the evaluation of the long term groundwater conditions at the
site will be presented in the CAP.
18.5 Geological and Hydrogeological Features influencing the
Movement, Chemical, and Physical Character of the
Contaminants
Groundwater flow is predominately in the north direction toward the Yadkin River. However,
there also is a component of groundwater flow to the west of Cell 1 and there is localized flow in
an area east of the source that requires further evaluation (between Cells 2 and 3).
Exceedances of COls have been observed in monitoring wells in these areas and near the ash
basin west compliance boundary. The exceedances, however, do not include COls identified by
the USEPA as indicators of CCR related contamination. Further, the constituents identified with
exceedances to the south, east and west of the source have also been identified in the
background wells.
The initial site conceptual hydrogeologic model presented in the Work Plan, dated December
30, 2014, indicated the geological and hydrogeological features influencing the movement,
chemical, and physical characteristics of contaminants are related to the Piedmont
hydrogeologic system present at the site. The movement of the contaminants is related to the
groundwater flow direction, the groundwater flow velocity, and the rate at which a particular
contaminant reacts with materials in the aquifer. The rate of groundwater movement varies with
the hydraulic conductivity and porosity of the site soil and rock materials and ranged from 5.3
ft/yr to 91.8 ft/yr in soils, and 4.0E-2 ft/yr to 2.29E-5 ft/yr in rock.
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Other factors include redox conditions, the concentration of the solution, the chemical
composition of the solution and the contaminant, and the mineralogy of the soil or rock matrix.
The influence of these factors as determined by the chemical, physical, hydrologic, and
mineralogical characterization of the ash, ash basin porewater, the groundwater, and the site
soil and rock will be incorporated into the groundwater modeling discussed in Section 13.0.
Geological and hydrogeological features at the site do not influence the physical character of
the constituents other than through the process of sorption and precipitation. The Kd term
development and the leaching test results, that will be presented in the CAP, will be key to
understanding the influences of the site soils and rock on the constituents.
The groundwater model will provide information to allow evaluation of the capacity of the site
soil and aquifer material to attenuate the loading imposed by the conditions modeled for the
proposed corrective action.
18.6 Proposed Continued Monitoring
A plan for continued monitoring of select monitoring wells and parameters/constituents is
presented in Section 16.0 and will be implemented following approval of this CSA report.
18.7 Preliminary Evaluation of Corrective Action Alternatives
In accordance with CAMA, Duke Energy is required to implement closure and remediation of the
Buck ash basin no later than August 1, 2029. Closure for the Buck ash basin was not defined in
CAMA. However, CAMA does require Duke Energy to submit a proposed CAP such that
NCDENR can prioritize site closure based on risk classifications.
No later than December 31, 2015, NCDENR is to develop proposed classifications for all coal
combustion residuals surface impoundments, including active and retired sites, for the purpose
of closure and remediation. At which time a schedule for closure and required remediation that
is based on the degree of risk to public health, safety and welfare, the environment, and natural
resources posed by the impoundments and that gives priority to the closure and required
remediation of impoundments that pose the greatest risk (CAMA 2014).
The classification for the Buck ash basin will be based upon this CSA and the corrective action
plan (CAP) which is to be submitted within 90 days of submittal of the CSA. The risk
classifications as described in CAMA include:
(1) High -risk impoundments shall be closed as soon as practicable, but no later than
December 31, 2019. A proposed closure plan for such impoundments must be submitted
as soon as practicable, but no later than December 31, 2016.
(2) Intermediate -risk impoundments shall be closed as soon as practicable, but no later
than December 31, 2024. A proposed closure plan for such impoundments must be
submitted as soon as practicable, but no later than December 31, 2017.
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(3) Low -risk impoundments shall be closed as soon as practicable, but no later than
December 31, 2029. A proposed closure plan for such impoundments must be submitted
as soon as practicable, but no later than December 31, 2018.
Following NCDENR's risk classification determination, a Closure Plan for the ash basin is to be
submitted for NCDENR's approval (CAMA 2014).
Based on the findings of this CSA report, the future CAP, NCDENR's risk classification, and the
approved Closure Plan, appropriate action will be taken for ash basin closure.
In the subsequent CAP, Duke Energy will pursue corrective action under 15A NCAC 02L .0106
(k) or (1) depending on the results of the groundwater modeling and the evaluation of the site's
suitability to use MNA. This would potentially require evaluation of MNA using the approach
found in Monitored Natural Attenuation of Inorganic Contaminants in Groundwater, Volumes 1
and 2 (EPA Reference) and the potential modeling of groundwater surface water interaction. If
these approaches are found to not be satisfactory, additional measures such as active
remediation by hydraulic capture and treatment, among others, would be evaluated. When
properly applied, alternatives such as these can provide effective long term management of
sites requiring corrective action.
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19.0 REFERENCES
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