In Re: Methyl Tertiary Butyl Ether ("MTBE") Products Liability Litigation
Filing
4625
MEMORANDUM OF LAW in Opposition re: (609 in 1:08-cv-00312-VSB-DCF) MOTION to Dismiss . . Document filed by New Jersey Department of Environmental Protection, The Commissioner of the New Jersey Department of Environmental Protection. (Attachments: # 1 Exhibit 1, # 2 Exhibit 2 part 1 of 4, # 3 Exhibit 2 part 2 of 4, # 4 Exhibit 2 part 3 of 4, # 5 Exhibit 2 part 4 of 4, # 6 Exhibit 3, # 7 Exhibit 4, # 8 Exhibit 5, # 9 Exhibit 6, # 10 Exhibit 7)Filed In Associated Cases: 1:00-cv-01898-VSB, 1:08-cv-00312-VSB-DCF.(Kaufmann, Leonard)
Exhibit 6
aquilogic, Inc.
245 Fischer Avenue, Suite D‐2
Costa Mesa, CA 92626, USA
Tel. +1.714.770.8040
Web: www.aquilogic.com
environment ● water ● strategy
REVISED SITE SUMMARY
ID # ‐ 8857 EXXON SERVICE
STATION #31310
Livingston Township, Essex County, New Jersey
Prepared on behalf of:
New Jersey Department of Environmental Protection (NJDEP)
The Commissioner of the NJDEP
The Administrator of the New Jersey Spill Compensation Fund
For:
The Office of the Attorney General of New Jersey
and
Miller, Axline & Sawyer
The Law Office of John K. Dema
Berger & Montague
Cohn Lifland Pearlman Herrmann & Knopf
Project No.: 003‐01
January 2013
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ID # ‐ 8857 Exxon Service Station #31310
January 2013
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TABLE OF CONTENTS
1.0
INTRODUCTION .......................................................................... 1
1.1
1.2
Project Objectives ............................................................................................. 2
History of MTBE Use in New Jersey .................................................................. 3
2.0
REGIONAL SETTING .................................................................... 5
2.1
2.2
2.3
2.4
2.5
Geologic Setting ................................................................................................ 5
Hydrogeologic Setting ....................................................................................... 6
Topography ....................................................................................................... 7
Climatic Setting ................................................................................................. 7
Groundwater Quality and Use .......................................................................... 8
3.0
SITE SETTING .............................................................................. 9
3.1
3.2
3.3
Site Description ................................................................................................. 9
Site Location ...................................................................................................... 9
Surface Cover and Drainage ............................................................................. 9
.
4.0
SITE HISTORY ............................................................................ 10
4.1
4.2
Operational History ......................................................................................... 10
Environmental Investigation and Remediation Chronology........................... 10
5.0
HYDROGEOLOGIC SETTING ....................................................... 32
5.1
5.2
5.2.1
5.2.2
5.2.3
5.2.4
5.3
5.3.1
5.3.1.1
5.3.1.2
5.3.2
5.3.2.1
5.3.2.2
5.3.3
5.3.3.1
Site Geology and Hydrogeology ...................................................................... 32
Unconsolidated Wells ..................................................................................... 33
Depth/Elevation .............................................................................................. 33
Flow Direction and Gradient ........................................................................... 34
Hydraulic Properties ....................................................................................... 34
Velocity ........................................................................................................... 34
Bedrock Wells ................................................................................................. 34
Zone A Wells ................................................................................................... 34
Zone A Depth/Elevation .................................................................................. 34
A Zone Flow Direction and Gradient .............................................................. 34
.
Zone B Wells.................................................................................................... 35
Zone B Depth/Elevation .................................................................................. 35
Zone B Flow Direction and Gradient ............................................................... 35
Zone C Wells ................................................................................................... 35
.
Zone C Depth/Elevation .................................................................................. 35
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5.3.3.2
5.3.4
5.3.4.1
5.3.4.2
5.3.5
5.3.6
Zone C Flow Direction and Gradient ............................................................... 36
Zone D Wells ................................................................................................... 36
Zone D Depth/Elevation ................................................................................. 36
.
Zone D Flow Direction and Gradient .............................................................. 36
Bedrock Hydraulic Properties ......................................................................... 36
Velocity ........................................................................................................... 37
6.0
CONTAMINANT CONDITIONS ................................................... 38
6.1
6.2
6.2.1
6.2.2
6.2.3
6.3
6.3.1
6.3.2
6.3.3
6.4
6.4.1
6.4.2
6.4.2.1
6.4.2.2
6.4.3
6.4.3.1
6.4.3.2
6.4.3.3
Chemicals of Concern ..................................................................................... 38
Soil and Soil Vapor Contamination ................................................................. 38
Nature ............................................................................................................. 38
Magnitude ....................................................................................................... 38
Extent .............................................................................................................. 39
LNAPL .............................................................................................................. 40
Nature ............................................................................................................. 40
Magnitude ....................................................................................................... 40
Extent .............................................................................................................. 40
Groundwater Contamination ......................................................................... 41
.
Nature ............................................................................................................. 41
Magnitude ....................................................................................................... 41
Unconsolidated Sediment Wells ..................................................................... 41
Bedrock Wells ................................................................................................. 42
Extent .............................................................................................................. 43
Unconsolidated Sediments ............................................................................. 43
Bedrock ........................................................................................................... 44
Summary of Plume Dimensions ...................................................................... 46
7.0
REMEDIATION .......................................................................... 48
8.0
FATE AND TRANSPORT ............................................................. 50
8.1
8.2
8.3
8.4
8.5
8.5.1
8.5.2
8.5.3
Physical and Chemical Properties of COCs ..................................................... 50
Sources ............................................................................................................ 51
Pathways ......................................................................................................... 52
Receptors ........................................................................................................ 53
Site Conceptual Model .................................................................................... 54
Hydrogeology .................................................................................................. 54
Releases .......................................................................................................... 54
Investigation and Remediation ....................................................................... 54
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8.5.4
8.5.5
8.5.6
8.5.7
COC Magnitude and Extent ............................................................................ 55
.
Pathways ......................................................................................................... 55
Receptors ........................................................................................................ 55
Summary ......................................................................................................... 56
9.0
DATA GAPS ............................................................................... 57
9.1
9.2
9.2.1
9.2.2
Hydrogeology .................................................................................................. 57
Contamination ................................................................................................ 57
Soil and Soil Vapor .......................................................................................... 57
Groundwater ................................................................................................... 57
10.0
KEY OPINIONS .......................................................................... 59
11.0
REFERENCES ............................................................................. 61
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LIST OF TABLES
1
Well Construction Details
2
Summary of Depth to Water
3
Regional Supply Well Analytical Results Summary
4
Chemical Properties of Fuel Oxygenates
5
Summary of Key Site Data
6
Summary of Key Opinions
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LIST OF FIGURES
1
Site Location Map
2
Site Plan
a Site Plan Detail
3
Site Characterization and Remedial Action Chronology
4
Regional Geological Map
5
Regional Cross Section
6
Site Cross Section
a Cross Section A‐A’
b Cross Section B‐B’
7
Groundwater Flow Direction
a Rose Diagram
i
Unconsolidated Sediments
b Groundwater Elevation
8
i
Unconsolidated Sediments
ii Bedrock
Summary of Analytical Results – MTBE in Groundwater
a Initial Assessment
b Pre‐Remediation
d Most Recent
9
Summary of Analytical Results – TBA in Groundwater
a Initial Assessment
b Pre‐Remediation
d Most Recent
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LIST OF APPENDICES
A
Groundwater Analytical Results (By Well)
B
Groundwater Analytical Results (By Date)
C
Time‐Series Hydrographs
D
Soil Data Table/s
E
Soil Vapor Table/s
F
Groundwater Contour Map
G
Kleinfelder Cross Sections, May 2009
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ACRONYMS AND ABBREVIATIONS
AG
AMSL
bgs
BTEX
BWA
CO
COCs
EDR
F
FS
GWP&T
GWQS
i
IAS
IASL
IGWSCC
K
kg
L
LEL
LNAPL
LPH
MCL
µg
µg/kg
µg/L
µg/m3
mg
mg/kg
MTBE
ne
NAAQS
NFA
NJDEP
NJPDES
NOD
O2
PA/SI
PCE
%
PID
ppb
PSW
RASR
Attorney General
above mean sea level
below ground surface
benzene, toluene, ethyl benzene, and total xylenes
Bureau of Water Allocation
carbon monoxide
chemicals of concern
Environmental Data Resources
Fahrenheit
Feasibility Study
groundwater pump and treat
groundwater quality standard
gradient
indoor air sampling
indoor air screening level
Impact to Groundwater Soil Cleanup Criteria
hydraulic conductivity
kilograms
Liter
lower explosive limit
light non‐aqueous phase liquid
liquid phase hydrocarbon
maximum contaminant level
micrograms
micrograms per kilogram
micrograms per Liter
micrograms per meter cubed
milligrams
milligrams per kilogram
methyl tertiary‐butyl ether
porosity
National Ambient Air Quality Standards
No Further Action
New Jersey Department of Environmental Protection
New Jersey Pollutant Discharge Elimination System
Notice of Deficiency
oxygen
Preliminary Assessment/Site Investigation
tetrachloroethene
percent
photo ionization detector
parts per billion
Public Supply Well
Remedial Action Selection Report
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RAW
RAWA
RDCSRS
RFG
RIR
RIW
SCM
SGSL
SRRA
SRS
State
STP
SVE
TBA
TCE
TIC
TPHg
USEPA
USGS
UST
VIIW
VOCs
WOF
WSW
Remedial Action Workplan
Remedial Action Workplan Addendum
Remedial Direct Contact Soil Remediation Standards
Reformulated Gasoline
Remedial Investigation Report
Remedial Investigation Workplan
site conceptual model
soil gas screening level
Site Remediation Reform Act
sensitive receptor survey
State of New Jersey
submersible turbine pump
soil vapor extraction
tert‐butyl alcohol
trichloroethene
Tentatively Identified Compound
total petroleum hydrocarbons gasoline
United States Environmental Protection Agency
United States Geological Survey
underground storage tank
Vapor Intrusion Investigation Workplan
volatile organic compounds
Wintertime Oxygenated Fuel
Water Supply Well
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1.0
INTRODUCTION
The State of New Jersey (the State) is blessed with precious and invaluable water resources ‐
both surface water and groundwater. These resources are held in trust, and used in many ways,
for the benefit of the people of the State. They also provide a safe, reliable, and sustainable
water supply for industrial, agricultural, and domestic purposes. In addition, these resources
sustain vibrant and valuable ecological habitats and have an inherent aesthetic value.
There are numerous facilities throughout the State that refine, store, or sell petroleum products.
Many of these facilities have documented releases of these products to the environment. In
many cases, these releases have polluted water resources.
In general, petroleum products, such as gasoline, are a mix of many individual chemical
compounds. The chemicals in gasoline are predominantly aliphatic and aromatic hydrocarbon
compounds (comprised of carbon and hydrogen atoms) derived from the refining of crude oil.
In addition, other chemicals are then added to gasoline to improve its performance.
Most of the hydrocarbon compounds in gasoline have a relatively limited impact on water
resources due to their fate and transport properties; that is, they do not migrate very far in the
environment and naturally biodegrade. However, due to its fate and transport properties (see
section 8.1), methyl tertiary butyl ether (MTBE) has a significant impact on water resources
when gasoline containing the chemical is released to the environment.
Given the widespread historical use of MTBE in gasoline in the State of New Jersey and the
propensity of the systems that store gasoline to leak, significant MTBE contamination of water
resources exists throughout the State. In particular, MTBE has been detected in numerous
public and private water supply wells (WSWs) across the State.
The State, notably the Department of Environmental Protection (NJDEP), has the authority and
responsibility to manage, protect and, where necessary, restore water resources in the State in
the interests of present and future citizens. The NJDEP directs those parties responsible for
pollution of water resources to implement programs to investigate and remediate their
contaminant releases.
Given the magnitude of the damage to water resources from MTBE contamination, and the
ongoing threat this contamination poses, the State Office of the Attorney General (AG) filed a
lawsuit on behalf of the people of the State against various companies considered responsible
for the contamination.
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The AG retained the following outside counsel to support them in this ligation: Miller, Axline &
Sawyer; the Law Offices of John K. Dema; Berger & Montague; and Cohn Lifland Pearlman
Herrmann & Knopf (collectively referred to herein as Plaintiff counsel).
Contamination by MTBE and tert‐butyl alcohol (TBA) has been detected at thousands of facilities
throughout the State. Addressing all of these facilities in one trial is impractical; therefore, a
finite number of “trial sites” have been selected by the defendants and plaintiffs to be the
subject of the first phase of litigation in this matter. The trial sites include 19 facilities and
defined areas in the immediate vicinity of the facilities where contamination is, or may be,
present.
1.1
Project Objectives
Amongst other things, the litigation brought by the State against the parties responsible for
MTBE contamination seeks to recover damages; that is, money or equitable relief, to restore
water resources impacted by MTBE and TBA.
Aquilogic has been retained by Plaintiff counsel to conduct the following:
1. Review available information about the 19 trial sites including, but not limited to, files from
the NJDEP and information provided by defendants;
2. Review available information for public and private WSWs in the vicinity of the trial sites
including, but not limited to, pumping records and chemical analyses;
3. Summarize available information and data for the above;
4. Analyze release history, hydrogeology, and contaminant presence at the trial sites;
5. Evaluate the nature, magnitude, and extent of contamination;
6. Develop a site conceptual model (SCM) that considers contaminant sources, pathways, and
receptors;
7. Identify data gaps and other deficiencies in the investigation and remediation programs
implemented at the trial sites;
8. Evaluate the programs needed to restore water resources impacted by releases at the trial
sites to their pre‐impacted condition;
9. Develop costs to implement these restoration programs; and
10. Proffer opinions at trial related to the above.
Therefore, the ultimate objective of our work is to develop costs (i.e. damages) to implement
programs to restore water resources contaminated by MTBE and TBA at the trial sites.
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This report addresses items 1 through 7 above, and presents opinions related to that work.
Supplemental documents (e.g. remediation feasibility studies [FS], restoration costs) address
items 8 and 9.
1.2
History of MTBE Use in New Jersey
MTBE usage in New Jersey began in the late 1970s (NJDEP, 2001). It was used as an octane
enhancer throughout the 1980s at low concentrations, primarily in high‐octane grade gasoline
(NJDEP, 2001). During this time, concentrations of MTBE in premium grade gasoline ranged
from 2% to 8%; regular grade gasoline contained a lower percentage (NJDEP, 2001).
In 1990, Congress passed amendments to the Clean Air Act (CAA) that mandated the use of
reformulated gasoline (RFG) and wintertime oxygenated fuel (WOF) in areas that had failed to
reduce ambient air quality to the National Ambient Air Quality Standards (NAAQS) (NJDEP,
2001). Specifically, the use of WOF during winter months was mandated for 39 urban areas
(including 2 areas comprising 21 counties in New Jersey) throughout the country to limit
emissions of carbon monoxide (CO), and RFG was mandated for 9 urban areas (including all but
2 counties in New Jersey) to limit emissions of contaminants that lead to the formation of ozone
(NJDEP, 2001). These fuels require the presence of oxygen at 2.7% by weight for WOF and 2%
by weight for RFG (NJDEP, 2001). MTBE was the primary gasoline additive used to meet the
mandated oxygen percentage (NJDEP, 2001). To meet the weight requirements, MTBE would
need to account for 15% by volume of WOF (almost 2.5 cups per gallon) and 11% by volume of
RFG (about 1.75 cups per gallon) (NJDEP, 2001).
The use of RFG was required beginning January 1, 1995. Although two counties were exempted
from this requirement, New Jersey mandated its use statewide in order to streamline gasoline
distribution (NJDEP, 2001).
The WOF program was established in the winter of 1992‐1993 in both northern and southern
New Jersey (NJDEP, 2001). In 1995, southern New Jersey attained the NAAQS for CO and
discontinued the WOF program (NJDEP, 2001). In 1997, the NJDEP submitted requests to the
United States Environmental Protection Agency (USEPA) to suspend the WOF program in
northern New Jersey, citing findings of MTBE risk to water supplies and citizen concerns about
the use of MTBE in gasoline (NJDEP, 2001). In 1999, the request was approved with the
condition that RFG would be sold during all months throughout New Jersey (NJDEP, 2001).
Upon initiating the WOF program, the state of New Jersey received numerous complaints
regarding MTBE (NJDEP, 2001). In 1995, citizens claimed that they felt sick when exposed to the
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15% MTBE WOF gasoline in fall and winter, and felt “great” during spring and summer months
when 11% MTBE RFG gasoline was used (NJDEP, 2001).
In 1996, the New Jersey drinking water, health‐based Maximum Contaminant Level (MCL) for
MTBE of 70 micrograms per Liter (µg/L) was established (NJDEP, 2001). An MCL of 70 µg/L is
also used for groundwater and surface water contamination (NJDEP website, 2012).
MTBE was first detected in a drinking WSWs in the 1980s (NJDEP, 2001). Sampling of public
WSWs collected during 1985 and 1986 indicated MTBE concentrations as high as 81 µg/L
(NJDEP, 2001). Regular sampling of public WSWs for MTBE commenced in 1997 upon
establishing the drinking water MCL (NJDEP, 2001). A survey conducted from 1997 to 1998 of
New Jersey water supplies indicated the presence of MTBE in 15% of the systems sampled
(NJDEP, 2001). Many individuals can smell and/or taste MTBE in drinking water at levels well
below 70 parts per billion (ppb) (NJDEP, 2007).
A survey of private drinking water supplies conducted in four areas of New Jersey in 1998
indicated the presence of MTBE in 35% of the wells sampled (NJDEP, 2001). Concentrations
ranged from 0.10 µg/L to 30.2 µg/L (NJDEP, 2001).
Studies conducted from 1994 to 1999 by the United States Geological Survey (USGS) indicated
the regular detection of MTBE in streams and lakes throughout New Jersey, with concentrations
ranging from 0.2 µg/L to 30 µg/L, all below the MCL (NJDEP, 2001).
In 2001, New Jersey estimated the number of gasoline underground storage tanks (USTs) in the
state to be around 34,000 (NJDEP, 2001). With an average capacity of 5,000 gallons (NJDEP,
2001) and a required 11% by volume of MTBE in RFG gasoline, this would account for
18,700,000 gallons of MTBE in USTs at any given time in 2001. New Jersey further reports that
half of the USTs closed in the state result in a reported discharge of hazardous substances and
half of the discharges impact groundwater (NJDEP, 2001). In 2001, MTBE was present at
concentrations above the MCL in 80% of the leaking UST cases in which groundwater had been
impacted (NJDEP, 2001).
In 2005, the New Jersey Legislature passed legislation banning the sale of gasoline that contains
more than 0.5% MTBE (NJDEP website, 2012). This law was effective January 1, 2009. Since
2006, most gasoline refiners have switched to using ethanol to increase oxygen percentage in
order to meet RFG standards (NJDEP website, 2012).
Reportedly, TBA has not been added to RFG, but is present in RFG as a bi‐product of the MTBE
refining process (0.02% on average) (EIA website, 2012), and as a breakdown product of MTBE.
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2.0
REGIONAL SETTING
The Livingston Exxon Service Station (the Site) is located at 38 East Mount Pleasant Avenue, in
Livingston Township, Essex County, New Jersey. The Site is within the Piedmont Physiographic
Province of New Jersey (Pristas, 2002). This province is a 1,600 square mile region bordered to
the northwest by the Highlands Province of New Jersey, to the northeast by the State of New
York and the Hudson River, to the southeast by the Coastal Plain Province of New Jersey, and to
the southwest by the state of Pennsylvania. The Site is approximately 15 miles west of
Manhattan, New York.
2.1
Geologic Setting
Bedrock geology of the Piedmont Physiographic province is characterized by normal‐faulted and
moderately dipping Late Triassic to Early Jurassic sedimentary rocks of the Newark Supergroup.
Locally, these strata are gently warped and broken by a few large faults and many small ones.
Newark Basin sediments mostly dip about 5 to 25 degrees to the northwest (Olsen, 1980). The
sedimentary rocks of the Newark Supergroup are fluvial and lacustrine deposits that in places
exceed 20,000 feet in thickness. Typical rock types include red conglomerate, sandstone, arkose
siltstone, shale, and argillite (Kleinfelder, 2010A,). The uppermost bedrock beneath the
Livingston Exxon Site is part of the Towaco Formation (NJDEP/NJGS, 2009), which is Lower
Jurassic in age and occurs in the middle of the Brunswick Group stratigraphic sequence (NJGS,
1990).
Paul E. Olsen, who is quoted on the Bedrock Geologic Map of the Caldwell Quadrangle of Essex
and Morris Counties, New Jersey, describes the lithology of the Towaco Formation as “reddish‐
brown to brownish‐purple sandstone, buff, olive‐tan, or light olive‐gray, fine‐ to medium‐
grained, micaceous sandstone, siltstone, silty mudstone in fining‐upward sequences 3 to 10 feet
thick… Siltstone is commonly planar laminated or bioturbated and indistinctly laminated to
massive.” Olsen’s published paper on the Triassic and Jurassic Formations of the Newark Basin,
details this formation as consisting of “laterally continuous symmetrical sedimentary cycles
about three to ten feet thick consisting of red, black, and gray sedimentary rocks with a central
black or gray microlaminated calcareous siltstone bound above and below by gray sandstone
and siltstone beds arranged in fining‐upwards cycles. Siltstone is commonly planar laminated or
bioturbated, but can be indistinctly laminated to massive” (Olsen, 1980). The regional siltstones
generally strike N45E with dips from 7 to 12 degrees and commonly have vertical fractures and
horizontal partings along bedding plains (Drake et aI., 1996).
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The unconsolidated surficial sediment at the Site is mapped as Late Wisconsinan glacial
lacustrine‐fan deposits of Pleistocene age (NJDEP/NJGS, 2009). The Surficial Geology Map for
the Caldwell Quadrangle (Stanford, 2005) identifies these deposits as fine‐ to coarse‐ sand and
pebble‐to‐cobble gravels, with minor fines, deposited during the Moggy Hollow stage of Lake
Passaic. Regionally, these deposits are up to 110 feet thick, but beneath the Site they range
from 25 to 50 feet thick, as described in Section 5.0.
2.2
Hydrogeologic Setting
Groundwater is supplied to the region from the Brunswick Aquifer and is stored and transmitted
within fractures in the Passaic, Towaco, Feltville, and Boonton formations (Herman et al., 1998).
The consolidated rocks of the Brunswick Aquifer contain both primary and secondary porosity;
however, the majority of the Brunswick Group has permeability due to secondary porosity (Sloto
et. aI., 1995). Well‐sorted and poorly cemented beds have the highest primary porosity;
whereas, poorly‐sorted and well cemented units have greatly reduced primary porosity. This
cementing causes the beds to be hard and brittle and contributes to the development of
fractures and joints (secondary porosity) (Kleinfelder, 2010A; SITE213‐008978).
The interbedded shales and sandstones of the Brunswick Aquifer are relatively impermeable
except where secondary porosity is present. Consequently, the interbedded shales and
sandstones have a low storativity and transmissivity. The fractures and joints that contribute to
this porosity constitute a small fraction of the total volume of rock, but are generally believed to
provide the principal conduits for groundwater flow (Kleinfelder, 2010A; SITE213‐008978).
“Fractured shales of the Brunswick Formation provide a major aquifer in the most industrialized
region of New Jersey. Numerous cases of ground water contamination have been documented in
this formation. However, effectiveness of monitoring and remediation efforts is often hampered
by the use of inappropriate concepts regarding ground water flow controls in this complex
aquifer system. One such concept presumes that near‐vertical fractures parallel to the strike of
beds provide principal passages for the flow and produce an anisotropic response to pumping
stress. Field evidence presented… confirms that the Brunswick Formation hosts a gently dipping,
multiunit, leaky aquifer system that consists of thin water‐bearing units and thick intervening
aquitards. The water‐bearing units are associated with major bedding partings and/or intensely
fractured seams. Layered heterogeneity of such a dipping multiunit aquifer system produces an
anisotropic flow pattern with preferential flow along the strike of beds….The commonly used
hydrogeologic model of the Brunswick as a one‐aquifer system, sometimes with vaguely defined
"shallow" and "deep" zones, often leads to the development of inadvertent cross‐flows within
monitoring wells. If undetected, cross‐flows may promote contaminant spread into deeper units
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and impair the quality of hydrogeologic data. Hydrogeologic characterization of the Brunswick
shales at any given site should be aimed primarily at identification of the major water‐bearing
and aquitard units” (Michalski, 1990). This model is based on the concept that hydraulic
connection occurs predominantly along more fractured stratigraphic units, i.e. discrete zones
controlled by bedding (Carswell and Rooney, 1976; Michalski, 1990; Hewitt, 1990).
A leaky multi‐unit aquifer system fits the flow patterns and heterogeneity of the individual beds
more closely than a one‐aquifer system with shallow and deep zones. The major bedding
partings and/or intensely fractured seams are the water bearing units within the system and are
separated by thick intervening aquitards (Kleinfelder, 2010A; SITE213‐008978).
2.3
Topography
The Site is situated at an elevation of approximately 325 feet above mean sea level (AMSL)
within a north‐south trending valley, between the second Watchung Ridge (elevation of about
600 feet AMSL) approximately two miles east of the Site, and a lower ridge (elevation about 450
feet AMSL) 0.7 miles to the west. The Site is located within the Upper Passaic River watershed
(Kleinfelder, 2010A; SITE213‐008978). Canoe Brook, which trends northeast to southwest near
the Site, is the nearest surface water at 800 feet to the southeast to 1,200 feet to the south
(USGS, 2011).
2.4
Climatic Setting
New Jersey has a moist, temperate climate with temperature variations throughout the year of
below 0 degrees Fahrenheit (F) to 100 degrees F or above. The northwestern Valley and Ridge
Physiographic Province will generally be slightly cooler due to its high altitude, while the densely
populated Piedmont Physiographic Province, where this Site is located, is slightly warmer due to
its lower elevation and urban heat island effects. The coldest regions in the state (the Northern
Highlands) have an average of 163 freeze free days, while the mild coastal regions have 217
freeze free days. Most regions in New Jersey receive between 43 and 47 inches of precipitation
annually. Although the Fall is the driest season in New Jersey, nor’easter low pressure systems
often form offshore, move up the coast, and inundate New Jersey with flooding rains and high
winds that can lead to considerable property damage and power outages between October and
April. Intense thunder storms and occasional tornadoes also occur in the spring and summer
(Rutgers University website, 2012).
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2.5
Groundwater Quality and Use
The groundwater from the Brunswick Aquifer is generally fresh, hard, slightly alkaline, and non‐
corrosive (Herman et al., 1998) and the local Livingston Township Water Department is currently
using 1,000,014,000 gallons of groundwater and 392,859,000 gallons of imported water from NJ
American (aquilogic, personal communication, September 12, 2012). Therefore, approximately
72% of water being used by the Livingston Township Water Department is from local
groundwater and 28% is imported.
A well search for the vicinity of the Site identified a public supply well (PSW), Livingston Well #11
(screened 54 to 423 feet below ground surface (bgs)), located approximately 1,750 feet to the
west‐northwest of the Site (Figure 1). A maximum MTBE concentration of 28.7 µg/L was
detected at this well on November 19, 2009. MTBE was not detected in subsequent samples
through May 2011 (Table 3). In addition, the closest commercial supply well is approximately
700 feet southwest of the Site at 19 South Livingston Avenue. A maximum MTBE concentration
of 14.5 µg/L was detected on October 28, 2004 at this well. The water in this well is used for
commercial cooling purposes. The well is screened from 28 to 298 feet bgs. There is also a
domestic supply well within 1,000 feet of the Site located at 35 N. Livingston Avenue, though it
is not currently in service as the owners of the well are using publicly provided water
(Kleinfelder, 2010A; SITE213‐008969).
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3.0
SITE SETTING
3.1
Site Description
The Site is an active Exxon Service Station with automotive repair services. The Site is located in
a mixed commercial and residential area of Livingston, New Jersey (Figure 1). The service
station is on a 0.39 acre parcel and consists of a service station building with garage bays, two
dispenser islands, and three USTs. Currently there is one 8,000‐, one 10,000‐, and one 12,000‐
gallon single‐walled fiberglass gasoline USTs located on the eastern portion of the station
(Kleinfelder, 2010A; SITE213‐008977 and SITE213‐008502).
3.2
Site Location
The Site is located at 38 East Mount Pleasant Avenue in Essex, New Jersey on the southwestern
corner of East Mount Pleasant and Sherbrooke Parkway (Figure 2). Commercial properties are
located to the east and west of the Site along East Mount Pleasant Avenue and residential
properties are located to the south. The area to the north of the Site across East Mount
Pleasant is a mix of commercial properties and residential condominiums. The notable
commercial property to the north of the Site is the Livingston Town Center (formerly known as
Livingston Manor and Park Plaza). Adjacent properties include a Prudential Insurance office
building to the east, residential properties to the south, and a retail strip mall to the west,
containing a shoe repair store, toy store, children's clothing store, and cellular service store
(Kleinfelder, 2010A; SITE213‐008977 to ‐008978).
3.3
Surface Cover and Drainage
The majority of the property is paved with either concrete or asphalt; however, there are a few
non‐paved landscaped areas located around the perimeter of the property (Kleinfelder, 2010A;
SITE213‐008977). There are three wide driveways connecting the Site to East Mount Pleasant
Avenue and Sherbrooke Parkway. Surface water drains to the north and west off Site to the
municipal storm water conveyance system along East Mount Pleasant Avenue (Kleinfelder,
2010A; SITE213‐008978).
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4.0
SITE HISTORY
4.1
Operational History
Historical records and the Essex County Assessor's office indicate that the Site operated as a
gasoline service station since at least 1934 (Kleinfelder, 2010B; SITE213‐009190). A 1934
Sanborn map indicates that the Site consisted of an eastern and western lot and three USTs
were located on the eastern parcel along East Mount Pleasant Avenue. The 1950 and 1962
Sanborn Maps indicate the Site still served as a gasoline station; however, the number and
locations of the USTs were not shown. In 1994, the township of Livingston updated their
property lot and block numbers and these two lots were combined into the current Block and
Lot number for this Site (Kleinfelder, 2010B; SITE213‐009200).
An Environmental Data Resources (EDR) City Directory search identified the Site as an Exxon
Service Station from at least 1975 (Kleinfelder, 2010B; SITE213‐009191). An ExxonMobil record
from 1979 indicated a total of six 4,000‐gallon steel gasoline USTs in the approximate location of
the current gasoline UST field, and a 1986 record showed three fiberglass USTs proposed for the
same location (Kleinfelder, 2010B; SITE213‐009193). The records suggest that the six steel tanks
were removed in October 1986 and were replaced with the three single‐walled (NJDEP, 2004B;
SITE213‐008782) fiberglass gasoline USTs (one 8,000‐, one 10,000‐ and one 12,000‐gallon) on
January 1, 1987. According to NJDEP records, these three gasoline tanks are still in use at the
Site (Figure 2a). (Kleinfelder, 2010B; SITE213‐009200).
In March of 2004, five 1,000‐gallon gasoline USTs that were previously abandoned‐in‐place were
identified and removed from the Site (Kleinfelder, 2010B; SITE213‐009200).
4.2
Environmental Investigation and Remediation Chronology
The following is a chronology of investigation and remediation activities that have been
conducted at the Site. Summaries of Site operations and characterization/remedial actions are
illustrated on Figure 3. Well construction details are summarized in Table 1, a summary of
depth to water for Site associated wells in Table 2, and regional well data is in Table 3.
Analytical results for Site associated wells are provided in Appendix A (by Well) and Appenidx B
(by Date).
Date/Period
October 1986
Activity
Six 4,000‐gallon steel unleaded gasoline USTs were reportedly removed
from the Site and replaced with three fiberglass gasoline USTs (one 8,000‐
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gallon, one 10,000‐gallon, and one 12,000‐gallon). These three USTs are
currently in use at the Site. Based on review of historical documents, it is
believed that the current fiberglass USTs were installed in the same location
as the six 4,000‐gallon steel USTs (Kleinfelder, 2010A; SITE213‐008969).
December 1993
A 1,000‐gallon fiberglass waste oil UST was removed under closure # C93‐
2553 (Kleinfelder, 2010A; SITE213‐008969).
February 1995
A UST Closure Assessment Report was submitted to the NJDEP on
February 23, 1995 for the December 1993 removal of a 1,000‐gallon waste
oil UST (Kleinfelder, 2010A; SITE213‐008969).
May 1995
A letter from the NJDEP dated May 8, 1995 granted No Further Action (NFA)
for the former waste oil UST that was removed on December 7, 1993 under
closure # C93‐2553. The NFA was based on analytical results of the soil
samples collected at the time of the UST removal. This letter referenced
NJDEP case # 94‐12‐09‐1551. The details of this NJDEP case number are not
known (Kleinfelder, 2010A; SITE213‐008969).
May 2001
A drive‐off at the regular dispenser occurred at the Site. “Less than one
gallon of gasoline was discharged to the pavement and to the pea gravel
beneath the dispenser island. The NJDEP was notified and case # 01‐05‐04‐
1325‐59 was assigned to the Site” (Kleinfelder, 2010A; SITE213‐008969).
The NJDEP Communication Center Notification Report noted a customer
drive off and a resulting spill of an unknown quantity and the presence of
soil contamination.
November 2001
A release of unknown quantity was reported when the 8,000‐gallon
gasoline UST was found to be leaking. Case # 01‐11‐13‐0846‐55 was
assigned (McCusker et al., 2005; SITE213‐008513).
Repairs were conducted on the flex line for the 10,000‐gallon UST.
Approximately one ton of pea gravel was removed from around the flex line
and hauled off Site for disposal (Kleinfelder, 2010A; SITE213‐008969).
December 2001
Site investigation activities commenced at the Site with the advancement of
14 geoprobe soil borings (SB‐1 through SB‐14) around the UST field and
dispenser islands. Results of the soil sampling indicated that benzene was
detected at concentrations exceeding the NJDEP Impact to Groundwater
Soil Cleanup Criteria (IGWSCC) in soil samples collected from soil borings
SB‐8, SB‐9, and SB‐13 (Kleinfelder, 2010A; SITE213‐008969). These borings
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were terminated due to refusal between 10 and 20 feet bgs, and no
groundwater was encountered.
January 2002
To characterize groundwater conditions at the Site, three monitoring wells
(MW‐1, MW‐2, and MW‐3) were installed using an air rotary rig in the
locations of geoprobe borings SB‐8, SB‐13, and SB‐4, respectively
(Kleinfelder, 2010A; SITE213‐008969). Groundwater was sampled on
January 29, 2002. MTBE was detected at concentrations of 153,000 µg/L
(MW‐1), 187,000 µg/L (MW‐2), and 11,000 µg/L (MW‐3).
February 2002
Light non‐aqueous phase liquids (LNAPL) was detected in monitoring well
MW‐1 (0.09 feet) located north of the current tank pit (Kleinfelder, 2010A;
SITE213‐008969).
Although LNAPL was not measured in MW‐2, benzene concentrations in
excess of 10,000 µg/L were detected in groundwater indicating the likely
presence of LNAPL to the south of the current tank pit.
As part of redevelopment activities at the property called Livingston Manor
(currently called Livingston Town Center), located northwest across Mount
Pleasant Avenue, three bedrock groundwater monitoring wells MW‐1
through MW‐3 were installed to total depths ranging from approximately
108.5 to 141 feet bgs. For purposes of this report, we have renamed these
wells as LMW‐1 through LMW‐3 to avoid confusion with on‐site wells
MW‐1, MW‐2, and MW‐3.
March 2002
A NJDEP Bureau of Water Allocation (BWA) well search (March 2002) and a
1,000‐feet radius manual well canvass (August 2002) were conducted as
part of a sensitive receptor survey (SRS) (Kleinfelder, 2010A; SITE213‐
008969). Several sensitive receptors were identified, including a total of five
public supply wells and two commercial supply wells within one mile of the
Site, and one domestic supply well within 1,000 feet of the Site. The
nearest public supply well, Livingston Well #11, is located 1,750 feet to the
northwest of the Site and screened from 54 to 423 feet bgs. “Based on
discussions with the property owner, the domestic supply well, located to
the northwest of the Site at 35 North Livingston Avenue, is not in service,
and the property is connected to public water.” The closest commercial
supply well is located approximately 700 feet southwest of the Site
at 19 South Livingston Avenue and is an active commercial supply well used
for machinery cooling purposes. This well is completed to a depth of 298
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feet with a screen interval from 28 to 298 feet bgs (Kleinfelder, 2010A;
SITE213‐008969).
Livingston Town Center bedrock monitoring wells LMW‐1 to LMW‐3 were
analyzed for benzene and a concentration of 21 µg/L was detected in
LMW‐3. The wells were not analyzed for MTBE during this sampling event.
May, June, and
LNAPL bailing events were conducted in May, June, and September 2002 to
address the LNAPL measured in MW‐1 (Kleinfelder, 2010A; SITE213‐
September 2002
008969). A total of 3.5 gallons of LNAPL were removed during these events
(Geologic Services Corporation, 2004A; SITE213‐001128).
January 2003
Six soil borings (SB‐15 through SB‐20) were advanced to further delineate
soil contamination detected at soil borings SB‐8 (MW‐2), SB‐9 and SB‐13
(MW‐2). Results of the soil sampling indicate that benzene, ethylbenzene,
and/or total xylenes were detected at concentrations above the NJDEP
IGWSCC or Remedial Direct Contact Soil Remediation Standards (RDCSRS) in
soil samples collected from soil borings SB‐15 through SB‐18 and SB‐20.
Three monitoring wells (MW‐4 through MW‐6) were installed to further
characterize groundwater conditions beneath the Site (Kleinfelder, 2010A;
SITE213‐008970). The Site soil data table is provided in Appendix D, herein.
February 2003
Livingston PSW #11 (screened from 54 to 423 feet bgs and located
approximately 1,750 feet west of the Site), was restarted by the Livingston
Water Department (Kleinfelder, 2010A; SITE213‐008970).
March 2003
LNAPL was detected in monitoring wells MW‐4 (0.17 feet) and MW‐6 (0.10
feet) (Kleinfelder, 2010A; SITE213‐008970).
MW‐4 is located approximately 33 feet northwest of MW‐1 near the
northeast corner of the property. MW‐6 is located on the western Site
property line, 146 feet southwest (down‐gradient) of MW‐1 and MW‐4.
Well MW‐6 is approximately 124 feet west of MW‐2. Therefore, it is likely
that LNAPL was present under much of the Site at this time.
Due to detections of benzene in LMW‐3 during the previous well sampling
at this Site, the property owner of Livingstone Manor, located across East
Mount Pleasant Avenue, installed additional wells MW‐4 and MW‐5. For
purposes of this report these wells have been renamed as LMW‐4 and
LMW‐5.
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April 2003
Activity
Groundwater samples from Livingston Manor wells LMW‐1 through LMW‐5
were analyzed for benzene, MTBE, and TBA. Three wells had MTBE and TBA
detections: LMW‐1 (screened 84 to 107 feet bgs), LMW‐2 (screened 110 to
135 feet bgs), and LMW‐3 (screened 115 to 141 feet bgs). The highest
concentrations were detected in Well LMW‐3: 5,500 µg/L MTBE and
1,800 µg/L TBA (EcolSciences, 2003; SITE213‐003506). LMW‐3 was located
350 feet down‐gradient (to the northwest) of Exxon well MW‐5 in the
direction of Livingston PSW #11. Well LMW‐2 was located 400 feet down‐
gradient of MW‐5; that is, 50 feet further down gradient from LMW‐3.
3,300 µg/L MTBE and 1,100 µg/L TBA were detected at LMW‐2.
Although a former gasoline service station was located on the Livingston
Manor property at the corner of North Livingston Avenue and East Pleasant
Avenue, it only operated until the 1940’s. MTBE was introduced to gasoline
in the late 1970’s (NJDEP, 2005; SITE790‐000347). Therefore, the MTBE and
TBA detected in groundwater cannot be associated with a release of
gasoline at this former station. No other sources for MTBE were identified
on the Livingston Manor property (NJDEP, 2005; SITE790‐000347).
ExxonMobil received notification that the Livingston PSW #11 was brought
back on‐line. ExxonMobil then initiated weekly gauging and bailing events
on the Site monitoring wells (Kleinfelder, 2010A; SITE213‐008970). During
the weekly LNAPL removal events, between April of 2003 and April 2004, a
total of 358 gallons of a mixture of LNAPL and groundwater was removed
from the Site.
During the initial LNAPL removal event at MW‐4, a maximum of 1.18 feet of
LNAPL was measured (4/30/2003).
May 2003
A dual‐phase extraction (DPE) pilot test was conducted at the Site to
determine if DPE was an appropriate remedial technology for the Site
(Kleinfelder, 2010A; SITE213‐008970).
Groundwater pump and treat (GWP&T) and soil vapor extraction (SVE)
feasibility tests were conducted on May 6, 2003 and June 11, 2003 to
evaluate the effectiveness of GWP&T and SVE as remedial technologies for
the Site (Kleinfelder, 2010A; SITE213‐008970).
Rising head slug testing was conducted using unconsolidated sediment
monitoring wells MW‐1, MW‐3, and MW‐6 as the test wells. The average
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hydraulic conductivity for the unconsolidated sediment aquifer was
calculated to be 3.805 feet per day (Kleinfelder, 2010A; SITE213‐008970).
June 2003
Bedrock monitoring well MW‐5D was installed to further characterize
groundwater conditions at the Site (Kleinfelder, 2010A; SITE213‐008970).
MTBE was detected at 21,000 µg/L at MW‐5D (screened 55 to 70 feet bgs)
during the initial sampling on July 1, 2003. This concentration is higher than
the maximum concentration ever detected in neighboring unconsolidated
sediment well MW‐5 (screened 25 to 45 feet bgs).
July 2003
Unconsolidated sediment monitoring wells MW‐7 and MW‐8 were installed
to delineate hydrocarbon and oxygenate impacted groundwater on‐Site
and for use in conjunction with the future GWP&T and SVE systems
(Kleinfelder, 2010A; SITE213‐008970).
LNAPL was detected in MW‐7 during groundwater sampling and LNAPL
bailing events. The maximum thickness of LNAPL detected in this well was
0.25 feet (8/19/2003). Although LNAPL was not detected in MW‐8, a
maximum benzene concentration of 13,100 µg/L (9/3/2003) was detected,
indicating that LNAPL was also likely present in the vicinity of this well. Both
MW‐7 and MW‐8 are located on‐site, down‐gradient of MW‐1, MW‐2, and
MW‐4 and up‐gradient of MW‐6.
September 2003
Up‐gradient well MW‐9 was installed in Sherbrooke Parkway.
November 2003
General Air Permit # GEN030001 was obtained from the NJDEP
Environmental Regulation, Air Permitting Program on November 13, 2003
(Kleinfelder, 2010A; SITE213‐008970).
March 2004
From March 19 to 30, 2004, five 1,000‐gallon gasoline USTs that were
previously abandoned‐in‐place were identified and removed from the Site
(Kleinfelder, 2010A; SITE213‐008970).
Bedrock monitoring well MW‐5D2 (screened 80 to 101 feet bgs) was
installed to further characterize deep groundwater conditions beneath the
Site. MW‐12D (screened 80 to 101 feet bgs) was installed to the northwest
of the Site across East Mount Pleasant Avenue on the Former Livingston
Manor property, in the direction of Livingston PSW #11. (Kleinfelder,
2010A; SITE213‐008970).
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During the April 2004 sampling event, MTBE concentrations were detected
at 2,810 µg/L in MW‐5D2 and at 1,070 µg/L in MW‐12D.
On March 25, 2004, the NJDEP issued a letter requiring ExxonMobil to
install at least eight additional groundwater monitoring wells to delineate
the horizontal and vertical extent of contamination in groundwater (NJDEP,
2004A; SITE213‐008899).
April 2004
Semi‐annual sampling of the commercial supply well (screened 28 to 298
feet bgs) located at the Bottle King liquor store (19 South Livingston
Avenue, 700 feet southwest of the Site) was initiated (Kleinfelder, 2010A;
SITE213‐008970). Benzene and MTBE were detected during this first
sampling event at 0.26 µg/L and 13.9 µg/L, respectively.
Semi‐annual vapor surveys began for subsurface utilities surrounding the
Site. Utility manholes and vaults were monitored for vapor organic carbons
(VOCs), % oxygen (O2), and % of lower explosive limit (LEL). (Kleinfelder,
2010A; SITE213‐002038). In April of 2006, these surveys became monthly
events until at least November 2006 where it appears that they became less
periodic. Further reporting of these events seem to be sporadic. Data
indentified for these activities is found in Appendix E.
May 2004
A field violation was issued by the NJDEP noting: “inaccurate registration”,
“liquid/free product in spill bucket”, and “Other: Delivery Ban. Do not fill
tanks. Contaminated soil found… run enhanced tracer test for UST system.”
(McCusker et al., 2005; SITE213‐008522)
“On May 26, 2004 Salomone Bros. Inc. conducted a visual inspection of all
Submersible Turbine Pump (STP) heads. Including the regular STP swift
check. The system was shut‐down and restarted for various portions of the
inspection. No visible spraying of liquid was observed at any STP. A weep
was observed at the regular STP swift check. A loose fitting was tightened
and the weeping ended… Less than one cubic foot of pea gravel was
removed during this work” (Drake, 2004; SITE213‐008910)
June 2004
At the request of the homeowner of 16 Sheerbrooke Parkway located
directly to the south of the Site, seven surface soil samples (Vitulli‐1
through Vitulli‐7) were collected at the residential property. The surface soil
sample analytical results indicated that the compounds analyzed were not
detected at or above their laboratory method detection limits (Kleinfelder,
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2010A; SITE213‐008970).
A soil data table indicated that all seven samples were collected from 0.5 to
1.0 feet bgs (Kleinfelder 2010C, SITE213‐009133).
July 2004
A New Jersey Pollutant Discharge Elimination System (NJPDES) Discharge to
Storm Sewer Permit request was submitted to the NJDEP ‐ Division of
Water Quality to discharge treated groundwater from the proposed
GWP&T system (Kleinfelder, 2010A; SITE213‐008970).
A last round of groundwater samples were collected from five monitoring
wells on the former Livingston Manor property prior to their abandonment
for the re‐development of the Site. MTBE was detected at concentrations
of 1,950 µg/L and 752 µg/L at wells LMW‐2 and LMW‐3, respectively. TBA
was detected at concentrations of 1,210 µg/L and 278 µg/L at wells LMW‐2
and LMW‐3, respectively.
No wells were ever installed down‐gradient of LM‐3 in the direction of
Livingston PSW #11.
The SVE system was installed and started using groundwater monitoring
wells MW‐1 through MW‐8 (Kleinfelder, 2010A; SITE213‐008970). The SVE
system was still operating as of September 2010. As of that time, a total of
12,475 lbs of hydrocarbons had been removed from the Site.
August 2004
Three indoor air samples were collected from 16 Sherbrooke Parkway using
24‐hour flow regulated summa canisters. Two air samples were collected
from inside the residential home, and one was collected from outside the
residential home. Results of the indoor air sampling indicate that MTBE was
detected above the NJDEP Indoor Air Screening (lAS) value. (Kleinfelder,
2010A; SITE213‐008970).
September 2004
The NJPDES B4B permit was approved by the NJDEP ‐ Division of Water
Quality (Kleinfelder, 2010A; SITE213‐008970).
A NJDEP letter was received requesting additional indoor air sampling,
sampling of the water within the basement sump, and a soil and
groundwater investigation at 16 Sherbrooke Parkway (Kleinfelder, 2010A;
SITE213‐008970).
Up‐gradient off‐site bedrock monitoring well MW‐9D (screened 55 to 80
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feet bgs) was installed in Sherbrooke Parkway and on‐site bedrock
monitoring well MW‐5D3 (screened 112 to 121 feet bgs) was installed.
Well MW‐5D3 was the deepest bedrock monitoring well ever installed, as
part of investigations at the Site. During the first sampling of MW‐5D3
(10/28/2004), MTBE was detected at a concentration of 24.2 µg/L in deep
bedrock groundwater on‐site. A year later, the maximum MTBE
concentration detected in this well was 512 µg/L.
October 2004
A geophysical investigation, including a down‐hole camera survey of the
open‐hole intervals within bedrock monitoring wells MW‐5D, MW‐5D2,
MW‐5D3, MW‐9D, and MW‐ 12D, was conducted to characterize bedrock
geology at the Site (Kleinfelder, 2010A; SITE213‐008971).
The limited data collected was inadequate to explain the hydrogeologic
conditions beneath the site; however, this study did note some high‐angle
fractures and an abundance of low‐angle “hairline fractures”.
MTBE and benzene were detected at 14.5 µg/L and 0.39 µg/L , respectively,
at the private well at 19 South Livingston Avenue, located approximately
700 feet to the southwest of the Site. These were the maximum
contaminant detections at this well.
As requested within the September 8, 2004 NJDEP letter, five air samples
were collected from 16 Sherbrooke Parkway utilizing 24‐hour flow
regulated summa canisters. Results of the indoor air sampling indicate that
MTBE was detected above the NJDEP Indoor Air Sampling (IAS) value in the
air samples collected from the basement, basement crawl space, the first
floor, sub‐slab and outside the house (Kleinfelder, 2010A; SITE213‐008971).
A water sample was collected from the basement sump of 16 Sherbrooke
Parkway. “The water sample analytical results indicated that targeted
compounds analyzed were either not detected at or above the laboratory
method detection limits or were detected at concentrations below the
NJDEP (Groundwater Quality Standard) GWQS” (Kleinfelder, 2010A;
SITE213‐008971).
November 2004
The Therm‐Tech CATVAC 25E catalytic‐oxidation (Cat‐Ox) SVE unit was shut
down due to a mechanical failure (Kleinfelder, 2010A; SITE213‐008971).
“A soil and groundwater investigation commenced at 16 Sherbrooke
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Parkway but was not completed due to encountered subsurface conditions.”
Soil samples for SB‐22 and SB‐23 were collected. The soil sample from SB‐23
had detections of ethylbenzene and xylenes between 14.5 to 15 feet bgs.
(Kleinfelder, 2010A; SITE213‐008971).
December 2004
The GWP&T system was activated utilizing eight groundwater monitoring
wells as extraction wells at a maximum pumping rate of two gallons per
minute (Kleinfelder, 2010A; SITE213‐008971). Groundwater was recovered
from MW‐1 through MW‐8 utilizing submersible pumps. All unconsolidated
sediment monitoring wells were converted to groundwater extraction wells
and no dedicated groundwater monitoring wells were ever reinstalled.
A drive‐off at a dispenser and a 5‐gallon release occurred at the Site. The
NJDEP was notified and case # 04‐ 12‐15‐1558‐52 was assigned (Kleinfelder,
2010A; SITE213‐008971).
January 2005
A Falco 300 Cat‐Ox unit was installed and started (Kleinfelder, 2010A;
SITE213‐008971).
A NJDEP letter was received requesting additional investigation of the
indoor air quality at 16 Sherbrooke Parkway (Kleinfelder, 2010A; SITE213‐
008971).
March 2005
A soil and groundwater investigation at 16 Sherbrooke Parkway was
conducted. Fourteen soil samples were collected from soil borings SB‐24
through SB‐30. The soil quality analytical results indicated that soil sample
SB‐25 (13.5‐14.0) was above the NJDEP IGWSCC for total xylenes. A
temporary passively‐placed, narrow diameter point was installed in soil
boring SB‐24 to collect a groundwater sample. The groundwater analytical
results indicated that benzene, total xylenes and tentatively identified
compounds (TICs) were detected at concentrations above the NJDEP
GWQS. (Kleinfelder, 2010A; SITE213‐008971).
April 2005
As requested within the January 28, 2005 NJDEP letter, five indoor air
samples were collected from 16 Sherbrooke Parkway. Results of the air
analysis indicate that benzene was detected above the IAS value in the air
samples collected from the basement. MTBE was detected above the NJDEP
IAS value in the air samples collected from the bathroom, and PCE was
detected above the NJDEP IAS value in the air samples collected from the
bathroom and the basement (4.4 micrograms per meter cubed (µg/m3))
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(Kleinfelder, 2010A; SITE213‐008971 to‐008972).
May 2005
A packer test was conducted on bedrock monitoring well MW‐5D2 to
determine the integrity of the seal between the steel casing and the
bedrock that extended to approximately 80 feet bgs. “Groundwater
samples were collected from above and below the packer to compare
groundwater quality concentrations. Results of the packer test indicated
that historical groundwater samples collected from MW‐SD2 may not be
representative of the groundwater quality from the open hole section of the
well and may be the result of the mixing of water leaking from the steel
casing and water entering the well from the vertical fracture at 95 to 97 feet
below grade” (Kleinfelder, 2010A; SITE213‐008972).
Although the groundwater may have been leaking from the upper casing,
it cannot be necessarily concluded that the groundwater traveling through
the vertical fracture at 95 to 97 is not impacted. In order to prove that the
water in the vertical fracture is not contaminated, a new well screened in
this interval must be installed properly. No well was reinstalled in this
area with the screen interval capturing the vertical fracture from 95 to 97
feet bgs.
August 2005
Monitoring wells MW‐10 (screened 8 to 30 feet bgs), MW‐10D (screened 50
to 72), MW‐11 (screen 9 to 30 feet bgs) and MW‐11D (screened 50 to 75)
were installed at 20 East Mount Pleasant Avenue to further characterize
groundwater conditions (Kleinfelder, 2010A; SITE213‐008972).
Although these wells were installed down‐gradient of known impacted
wells, none of these new wells were screened deep enough to delineate
lateral MTBE concentrations detected in MW‐5D2 (screened 80 to 101 feet
bgs) or MW‐5D3 (112 to 121 feet bgs). Except for three monitoring events
in MW‐10, both MW‐10 and MW‐11 were consistently dry.
September 2005
Monitoring well MW‐13 was installed on the property located at 16
Sherbrooke Parkway to further characterize groundwater conditions to the
south of MW‐2 (Kleinfelder, 2010A; SITE213‐008972).
MW‐13 was successful in delineating shallow groundwater contamination in
unconsolidated sediments cross‐gradient of the Site to the south. However,
as vertical delineation in the vicinity of MW‐2 and MW‐13 had not been
demonstrated, bedrock groundwater contamination is not delineated to the
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south of the Site.
December 2005
On December 8, 2005, a meeting was held between representatives of the
NJDEP, ExxonMobil, and Kleinfelder. ExxonMobil and the NJDEP agreed that
additional monitoring wells would be installed along strike and down dip
from the Site and that indoor air monitoring would be conducted at the
commercial property to the west of the Site (Kleinfelder, 2010A; SITE213‐
008972).
April 2006
The NJDEP Bureau of Emergency Response prepared a report regarding a
request for assistance. A Bell fiber optic cable box was reported to have
50% LEL readings in the area of a gas station located at 38 East Mount
Pleasant Avenue. A map showing these concentrations is included in
Appendix E.
UST system upgrade activities were conducted, including replacement of
the dispensers and product piping to the top of the USTs. A total of 122.33
tons of soil were removed from the Site. A total of 14 soil samples (DI‐1
through DI‐6 and PP‐1 through PP‐8) were collected from beneath the
dispensers and product piping (Kleinfelder, 2010A; SITE213‐008972].
May 2006
Indoor air screening, utilizing a portable photo ionization detector (PID),
was conducted in the basements of the commercial properties located at 20
and 24 East Mount Pleasant Avenue. Results of the air screening indicate
that VOCs were not detected above background levels in either basement
(Kleinfelder, 2010A; SITE213‐008972).
August 2006
“Representatives of the NJDEP, Kleinfelder, and Verizon, conducted a Site
visit on August 23, 2006 to investigate the Verizon utility/manholes (MH‐3
through MH‐6). Manholes MH‐3 through MH‐6, MH‐11 and MH‐12 were
screened for percent LEL. LEL readings for each manhole were 0%. In
addition, water samples were collected from each manhole and analyzed for
VO+10. Based on the results of the manhole water sampling, the compounds
analyzed in each manhole water sample were not detected at or above their
laboratory method detection limits” (Kleinfelder, 2010A; SITE213‐008972).
October 2006
Bedrock monitoring well MW‐5D2 (screened from 80 to 100 feet bgs) was
abandoned due to the integrity of the grout seal around the steel casing.
Bedrock monitoring well MW‐5D2R (screened 70 to 85 feet bgs) was
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installed to replace MW‐5D2 (Kleinfelder, 2010A; SITE213‐008972).
The casing of MW‐5D2 was determined to have been leaking since
May 2005; however, it was not abandoned until October of 2006. If
indeed the casing was leaking groundwater from shallower zone into the
screen interval, Well MW‐5D2 could have been functioning as a conduct
for contaminant migration into the deeper aquifer for up to 31 months
(well abandoned). In addition, when MW‐5D2R was replaced, the screen
interval was different and did not capture the vertical fracture between
95 and 97 which was noted during the packer test as a potentially
transmissive interval for groundwater flow. No fluid logging or other in‐
well tests were conducted to determine groundwater occurrence prior to
bedrock well installation.
Monitoring well MW‐15S (screened 10 to 30 feet bgs) and bedrock
monitoring well MW‐15D (screened 40 to 65 feet bgs) were installed at 6
West Mount Pleasant Avenue (Federated Church of Livingston) to further
characterize groundwater conditions off‐site to the west.
Soil boring SB‐31 was advanced in Sherbrooke Parkway to complete
horizontal delineation of the adsorbed‐phase hydrocarbon contamination
to the east of former soil boring SB‐25. (Kleinfelder, 2010A; SITE213‐
008972).
January 2007
“Step‐drawdown and constant‐rate pumping tests, using MW‐5D as the
extraction well, were conducted on January 15 and 16, 2007, respectively.
Results of the pumping tests indicate the maximum sustainable pumping
rate for MW‐5D was 2.5 gallons per minute and that the water‐bearing
fractures in monitoring wells MW‐5D (screened 55 to 70 feet bgs), MW‐9D
(screened 55 to 80 feet bgs) and MW‐11D (screen 50 to 75 feet bgs)
exhibited connectivity. Hydraulic conductivity and specific storage for the
bedrock aquifer fractures were estimated to be 0.9378 foot per day and
6.88E‐12 per foot, respectively, and hydraulic conductivity and specific
storage for the bedrock aquifer matrix were estimated to be 9.678E‐6 foot
per day and 2.837E‐8 per foot, respectively. Monitoring well MW‐5D3
(screened 112‐121 feet bgs) did not exhibit a water level response during
the pumping test and the fractures in this well do not appear to be
connected to those in MW‐5D (screened 55 to 70 feet bgs). Data collected
from monitoring wells MW‐5, MW‐5D2R, MW‐10D, MW‐12D and MW‐15D
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were inconclusive.” (Kleinfelder, 2010A; SITE213‐008972 and ‐008973)
May 2007
“On May 10, 2007, a meeting was held between representatives of the
NJDEP, ExxonMobil, and Kleinfelder. ExxonMobil and the NJDEP agreed that
additional monitoring wells would be installed along strike from the Site and
an evaluation of vapor intrusion of chlorinated solvents into the commercial
property to the west of the Site would be conducted” (Kleinfelder, 2010A;
SITE213‐008972).
“Active remediation of the bedrock aquifer did not begin until May 2007,
when monitoring well MW‐5D was connected to the GWP&T system as an
extraction well for the shallow bedrock aquifer.”(Kleinfelder, 2010A;
SITE213‐008992). An email dated November 28, 2007 from Gary A. Slater
from the NJDEP asked William E. Gottobrio from Kleinfelder if they had
begun “pumping from 5D yet?” Gottobrio responded that they had “been
pumping from MW‐5D since November 8, 2007.”
July 2007
Off‐site unconsolidated sediment monitoring well MW‐14S and bedrock
monitoring well MW‐14D were installed at 53 East Mount Pleasant Avenue
to further characterize groundwater conditions up‐gradient (Kleinfelder,
2010A; SITE213‐008973).
August 2007
A Remedial Action Workplan (RAW)/ Remedial Investigation Report (RIR)/
Remedial Investigation Workplan (RIW) was submitted to the NJDEP
(Kleinfelder, 2010A; SITE213‐008973).
April 2008
Two soil borings, SB‐34 and SB‐35, were advanced on April 29, 2008 to
delineate adsorbed phase hydrocarbon contamination. Soil samples were
collected at depths ranging from 11.5 to 19.0 feet bgs. The sample from SB‐
34 at 13 to 13.5 feet bgs had toluene concentrations above NJDEP IGWSCC
(Kleinfelder, 2010A; SITE213‐008973).
October 2008
The scheduled semi‐annual sampling at the commercial supply well was not
conducted in October 2008 due to property access issues. An amendment
to the access negotiated for monitoring well installation in the Bottle King
parking lot was prepared by ExxonMobil’s outside legal counsel (Kleinfelder,
2010A; SITE213‐008973).
A voicemail was left for the NJDEP Case Manager on October 13, 2008,
informing him of the access issues related to the commercial supply well
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sampling at the Bottle King property (Kleinfelder, 2010A; SITE213‐008973).
A meeting between representatives of the Livingston Town Center and
Kleinfelder was held to initiate access for the installation of a monitoring
well on the Livingston Town Center property (Kleinfelder, 2010A; SITE213‐
008973).
November 2008
Four bedrock monitoring wells MW‐16D (screened 50 to 70 feet bgs), MW‐
16D2 (screened 75 to 95 feet bgs), MW‐17D (screened 50 to 70 feet bgs),
and MW‐17D2 (screened 75 to 95 feet bgs) were installed along strike on
the Bottle King property to further delineate dissolved‐phase contamination
down‐gradient of the Site (Kleinfelder, 2010A; SITE213‐008973).
A Notice of Deficiency (NOD) dated November 13, 2008 for the RAW dated
August 29, 2007, and RIR/RIWs dated August 29, 2008; August 30, 2007;
March 5, 2007; September 3, 2006 and August 29, 2005 was issued by the
NJDEP on November 25, 2008 (Kleinfelder, 2010A; SITE213‐008973). In
summary, the letter required the following: re‐installation of MW‐10 and
MW‐11, re‐installation of Livingston Manor Wells MW‐2 and MW‐3 (LMW‐2
and LMW‐3), installation of vapor monitoring points to evaluate the
effectiveness of the SVE system, submission of a bedrock surface contour
map, a cross section of MW‐11 to MW‐14 with the building basement
footprint, and a proposal for an acceptable remedial action for the bedrock
aquifer.
December 2008
A RIW was submitted to the NJDEP on December 23, 2008 in response to
the November 13, 2008 NOD (Kleinfelder, 2010A; SITE213‐008973).
January 2009
A letter dated January 16, 2009 was received from the NJDEP approving the
December 23, 2008 RIW (Kleinfelder, 2010A; SITE213‐008973).
February 2009
Legal access to the Bottle King building to resume sampling of the
commercial supply well was obtained (Kleinfelder, 2010A; SITE213‐008973).
March 2009
Access to the properties located at 20‐24 East Mount Pleasant Avenue for
the purposes of conducting a vapor intrusion investigation, was granted on
March 5, 2009 (Kleinfelder, 2010A; SITE213‐008974).
A building walkthrough of the properties located at 20 ‐ 24 East Mount
Pleasant Avenue was conducted on March 24, 2009 as part of the vapor
intrusion investigation at the retail properties located adjacent to the Site
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to the west (Kleinfelder, 2010A; SITE213‐008974).
Two soil borings (SB‐38 and SB‐39) were advanced on March 27, 2009 via
direct push drilling techniques to depths of 19 and 20 feet bgs, respectively,
where refusal was encountered. Four soil samples were collected and
submitted for laboratory analysis for VO+10 (Kleinfelder, 2010A; SITE213‐
008974). The analytical data for oxygenates was not reported on soil data
tables and the laboratory report could not be located.
No hydrocarbons were detected in the soil samples from SB‐38. Low
detections of toluene, ethylbenze, and xylenes were detected in SB‐39 at
16.0 to 16.5 feet bgs.
Monitoring wells MW‐10 and MW‐11 which were consistently dry since
installation in August 2009, were redrilled to a depth of 49 feet bgs on
March 27 and 30, 2009. Open hole intervals were verified by the NJDEP via
phone conversations on March 27, 2009, prior to completion. The
replacement wells are identified as MW‐10R and MW‐11R, respectively.
MW‐10R and MW‐11R were not developed at the time of installation
because an insufficient amount of water was present in the wells
(Kleinfelder, 2010A; NJDEP‐SITE213‐008974).
April 2009
“MW‐10R and MW‐11R were sampled on April 14, 2009. Attempts were
made to develop the two monitoring wells prior to sampling, but were
unsuccessful due to an insufficient amount of water in the wells, and poor
recharge” (Kleinfelder, 2010A; SITE213‐008974). It is unclear if these wells
were ever properly developed.
Semi‐annual sampling of the commercial supply well at the Bottle King
resumed on April 14, 2009 (Kleinfelder, 2010A; SITE213‐008974).
May 2009
Soil borings SB‐36 was drilled and sampled within East Mount Pleasant
Avenue. SB‐37 through SB‐39 were completed as vapor monitoring points
VP‐1 through VP‐3 (Kleinfelder, 2010A; SITE213‐008974). These vapor
monitoring points were requested by the NJDEP to augment the monitoring
of the remedial system performance on a monthly basis (Kleinfelder,
2010A; SITE213‐008986).
A RIR/ Remedial Action Selection Report (RASR)/ RIW was submitted to the
NJDEP on May 21, 2009, in response to the November 13, 2008 NOD.
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(Kleinfelder, 2010A; SITE213‐008974).
June 2009
A Vapor Intrusion Investigation Workplan (VIIW) for the properties located
at 20 ‐ 24 East Mount Pleasant Avenue was submitted to the NJDEP on
June 25, 2009 (Kleinfelder, 2010A; SITE213‐008974).
July 2009
A SCM report was submitted to the NJDEP based on the data collected
during the 2004 down‐hole geophysical logging and the results of the 2007
aquifer testing. This report summarized the three‐dimensional bedrock
model of the Site and surrounding areas and summarized that the bedding
plane fractures recorded in MW‐5D3 could be projected to intersect former
wells LMW‐2 and LMW‐3 (Kleinfelder, 2010A; SITE213‐008974). “The
current conceptual model for groundwater flow within the bedrock is
predominately along strike with a lesser flow component down dip… the
former LMI (Livingston Manor) wells were located down dip” (Kleinfelder,
2009A; SITE213‐003268). The report recommended the installation of
groundwater monitoring wells on the former Livingston Manor property to
characterize bedrock groundwater flow and contaminant transport.
No wells have been installed on the former Livingston Manor property to
date.
August 2009
A RIR and a RIW was submitted.
The former Livingston Manor Wells MW‐1 through MW‐5 (LMW‐1 through
LMW‐5) were relabeled as PLAZA‐1 to PLAZA‐5 by the Site consultant and
PLAZA‐4 and PLAZA‐5 (LMW‐4 and LMW‐5) were miss‐located
approximately 200 feet to the west on the consultant’s figures.
September 2009
A letter dated September 15, 2009 which approved the June 25, 2009 VIIW
was received from the NJDEP on September 25, 2009 (Kleinfelder, 2010A;
SITE213‐008974).
October 2009
Indoor air and ambient air samples were collected from the properties
located at 20 – 24 East Mount Pleasant Avenue on October 19, 2009. The
collection of sub‐slab vapor samples was initiated on October 20, 2009, but
was cancelled due to painting occurring in one of the units. The results of
the vapor intrusion investigation activities were submitted to the NJDEP on
November 16, 2009 via electronic mail (Kleinfelder, 2010A; SITE213‐008974
to 008975).
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Activity
A maximum detection of 28.7 µg/L MTBE was detected in groundwater
sampled from Livingston PSW #11.
“A request for an extension of the deadline to submit a revised RAW from
December 31, 2009 to June 30, 2010 was submitted to the NJDEP on
November 16, 2009.” (Kleinfelder, 2010A; SITE213‐008975).
“Kleinfelder met the NJDEP Case Manager on Site on November 17, 2009 to
conduct a walkthrough of the commercial properties located at 20 ‐ 24 East
Mount Pleasant Avenue, and discuss the sampling locations. Kleinfelder re‐
mobilized to the properties located at 20 ‐ 24 East Mount Pleasant Avenue
to conduct a second round of indoor air and ambient air sampling, in
conjunction with sub‐slab vapor sampling during the period of November 19
‐ 21, 2009. The results of the vapor intrusion investigation activities were
submitted to the NJDEP on December 8, 2009 via electronic mail.”
(Kleinfelder, 2010A; SITE213‐008975).
December 2009
Kleinfelder contacted the NJDEP regarding the status of the
November 16, 2009 extension request for the revised RAW submittal on
December 29, 2009. The NJDEP case manager stated that due to the Site
Remediation Reform Act (SRRA) regulation changes, extension requests for
report deadlines were being automatically approved, unless the NJDEP
specifically issued a letter denying the extension request. The NJDEP case
manager stated that a denial of the extension request for the revised RAW
was not being prepared (Kleinfelder, 2010A; SITE213‐008975).
January 2010
A NOD dated January 11, 2010 was issued by the NJDEP. The NOD stated
that further evaluation of the vapor intrusion pathway to determine the
source of trichloroethene (TCE) detected in indoor air and sub‐slab vapor
samples was necessary. The NOD required a RIW to evaluate potential
sources of the elevated TCE concentrations detected in indoor air and sub‐
slab vapor samples collected from the properties located at 20 ‐ 24 East
Mount Pleasant Avenue within 30 days of receipt of the letter. The NOD
also required a site investigation to determine the source of PCE and TCE
detected in groundwater at the Site within 270 days of the date of the letter
(Kleinfelder, 2010A; SITE213‐008975).
February 2010
A Vapor Migration RIW/NOD Response report was submitted to the NJDEP
on February 12, 2010 in response to the January 11, 2010 NOD.
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“Six soil borings were advanced at the Site, and a total of eight soil samples
were collected as part of Phase II divestment activities during the period of
February 12, 2010 through February 16, 2010. Analytical results of the soil
samples indicated that benzene, ethyl benzene, total xylenes and TICs were
detected at concentrations exceeding the NJDEP and/or NJDEP RDCSCC in
soil samples SB‐1 (16.5‐17) and SB‐2 (17.5‐18). The targeted analytes were
not detected at concentrations exceeding the applicable NJDEP Soil Cleanup
Criteria in the remaining six soil samples.” (Kleinfelder, 2010A; SITE213‐
008975).
Both SB‐1 (2010) and SB‐2 (2010) are in the vicinity of the current USTs.
March 2010
Groundwater samples were collected from existing Site monitoring wells as
part of the Phase II divestment activities on March 30, 2010. Analytical
results of the soil samples indicated that benzene, toluene, ethyl benzene,
total xylenes (BTEX) and/or MTBE were detected in samples collected from
monitoring wells MW‐1 through MW‐4, MW‐7, and MW‐8 at
concentrations exceeding the NJDEP GWQS. Additionally, lead was detected
in the sample collected from MW‐4 at a concentration of 14.9 ug/L,
exceeding the NJDEP GWQS of 5 ug/L (Kleinfelder, 2010A; SITE213‐008975).
April 2010
A meeting between the NJDEP, ExxonMobil and Kleinfelder was held at
Kleinfelder's office on April 29, 2010. The SCM and proposed monitoring
well locations on the Livingston Town Center property were discussed. It
was Kleinfelder's and ExxonMobil's understanding that the NJDEP would
rank the list of well locations discussed during the meeting based on their
preference of location(s) (Kleinfelder, 2010A; SITE213‐008975).
May 2010
The May 21, 2009 RIR/ RASR/ RIW was approved in a letter from the NJDEP
dated May 6, 2010 (Kleinfelder, 2010A; SITE213‐008975).
The February 12, 2010, Vapor Migration RIW/NOD Response report was
approved in a letter from the NJDEP dated May 6, 2010 (Kleinfelder, 2010A;
SITE213‐008975).
A Remediation Timeframe Extension Request Form was submitted to the
NJDEP on May 27, 2010. This form requested an extension of the submittal
date for the RAW from June 30, 2010 to December 31, 2010 (Kleinfelder,
2010A; SITE213‐008976).
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June 2010
Activity
A meeting between Kleinfelder and EcolSciences (consultant for the
Livingston Town Center) was held at Kleinfelder's office on June 2, 2010.
The SCM and proposed monitoring well locations on the Livingston Town
Center property were discussed (Kleinfelder, 2010A; SITE213‐008976).
“Kleinfelder met with the owners of the properties located at 20 ‐ 24 East
Mount Pleasant Avenue on June 14, 2010 to discuss the scopes of work
proposed in the May 21, 2009 RIR/ RASR/ RIW and the February 12,2010
Vapor Migration RIW/NOD Response, which were approved by the NJDEP in
letters dated May 6, 2010. During this meeting, the property owners
requested that the vapor migration investigation work be postponed until
the findings of the (Preliminary Assessment/Site Investigation) PA/SI were
available, and that the system upgrade activities proposed to be conducted
on their property be delayed until approximately October 2010. The NJDEP
was informed of the property owners' requests on June 15, 2010”
(Kleinfelder, 2010A; SITE213‐008976).
July 2010
An email correspondence was received from the NJDEP on July 22, 2010
regarding the vapor migration investigation and system upgrade work
proposed to be conducted on the property located at 20 ‐ 24 East Mount
Pleasant Avenue. The email indicated that the NJDEP had facilitated access
to this property. The NJDEP required an updated schedule of activities
associated with the vapor migration investigation within seven days.
Requests for access were sent to the owners of the property located at
20‐24 East Mount Pleasant Avenue on July 26, 2010 for the purpose of
conducting the vapor migration investigation activities proposed in the
February 12, 2010 Vapor Migration RIW/ NOD Response report. Signed
access agreements were received from the property owners on August 6,
2010 and August 12, 2010 (Kleinfelder, 2010A; SITE213‐008976).
An updated schedule of activities for the vapor migration investigation and
system upgrade was submitted to the NJDEP via email on July 29, 2010
(Kleinfelder, 2010A; SITE213‐008976).
August 2010
The owner of the property located at 20 East Mount Pleasant Avenue
contacted Kleinfelder on August 17, 2010 and indicated that he was
entering the busiest time of year with back to school sales, and could not
afford the loss of parking spots or disruption to the business for at least the
next three weeks. The property owner indicated that the utility mark out
could proceed, but that drilling would not be permitted at that time, and
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that he would contact the NJDEP case manager directly to discuss the issue.
The NJDEP was notified of this on August 18, 2010 (Kleinfelder, 2010A;
SITE213‐008976).
Kleinfelder met with the owners of the property located at 20 ‐ 24 East
Mount Pleasant Avenue on August 26, 2010. A date of October 11, 2010
was agreed upon as the date when subsurface work for the vapor migration
investigation and remediation system upgrade would commence on that
property. The NJDEP was notified on September 1, 2010 (Kleinfelder,
2010A; SITE213‐008976).
A soil investigation was conducted as part of the SI in response to the
January 11, 2010 NOD during the period of August 31 to September 2,
2010. Seven borings were advanced to investigate potential impact from
historical automotive repair operations at the Site, the reported former
waste oil UST, associated oil‐water separator, and sewer line. Two surficial
soil samples were collected ‐ one from beneath each of two hydraulic lift
vents ‐ along the southern side of the station building (Kleinfelder, 2010A;
SITE213‐008976).
September 2010
A RIR/ RAW Addendum was submitted to the NJDEP on September 29, 2010
with a proposal to install an extraction well in the southeast corner of the
property located at 20 ‐ 24 East Mount Pleasant Avenue, and to connect off
Site monitoring wells MW‐10D, MW‐10R, MW‐11D, MW‐11R and a newly
installed extraction well to the existing GWP&T system. (Kleinfelder, 2010A;
SITE213‐008996). “… dissolved phase hydrocarbon recovery trend graphs
prepared for the GWP&T… indicate that hydrocarbon mass recovery has not
reached asymptotic conditions…” (Kleinfelder, 2010A; SITE213‐008986).
The former Livingston Manor Wells LMW‐1 through LMW‐5 continued to
be miss‐located approximately 200 feet to the west on the consultant’s
figures.
January 2011
A Site Status Update was submitted by ExxonMobil indicating that a new
recovery well, and the MW‐10 and MW‐11 cluster wells, would be added to
the remediation system. The new recovery well named RW‐18 was installed
to 78 feet bgs; however, “initial review of the completed well indicates that
RW‐18 may not be viable, as on November 18, 2010 the well was gauged to
a terminal depth of 62.5 feet bgs on mud. This suggests that either the
open‐hole interval collapsed or it has become impacted with sediment from
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the formation during the stabilization period” (ExxonMobil, 2011; SITE213‐
008523).
February 2011
An Initial Receptor Survey Evaluation Form was submitted. Eight residences
were located within 200 feet of the Site. Additionally, the supporting
documents indicated that four vapor probes (VP‐4 to VP‐7) had been
installed on the property to the west of the Site at 20‐24 Mount Pleasant in
October of 2010. After installation, they were not deemed as appropriate
vapor points by ExxonMobil as they were observed to be under vacuum by
the remediation system (Kleinfelder, 2011; SITE213‐008448).
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5.0
HYDROGEOLOGIC SETTING
5.1
Site Geology and Hydrogeology
The geology beneath the Site consists of unconsolidated silt and fine sand grading to coarse
sand up to an approximate depth of 30 feet bgs and then coarse sands and gravels to bedrock at
approximately 45 feet bgs. Underlying these unconsolidated sediments are the interbedded
gray and red to reddish‐brown siltstones of the Towaco Formation. The siltstones are generally
located with upward fining sequences one to three meters thick and are commonly planar‐ or
cross‐ laminated. “Bedrock topography in the vicinity of the Site is irregular with the top‐of‐
bedrock elevation ranging from around 300 to 250 feet AMSL” (Kleinfelder, 2010A). Siltstones
commonly have vertical fractures and horizontal partings along bedding planes (Drake et aI.,
1996). The United States Geological Survey (USGS) Bedrock geology map for Essex and Morris
Counties by R. A. Volkert shows the nearest measured attitude of the Towaco Formation being a
¼ mile to the west with a strike of N14E and dip of 7° to the northwest with the mean strike of
the sedimentary bedding in these counties reported as N19E (Volkert, 2006) with a dip between
7 and 12°(Drake et aI., 1996). Regional geology is presented on Figure 4 and a regional cross
section is illustrated on Figure 5.
The nature of groundwater occurrence and flow characteristics have not been adequately
assessed beneath the Site; however, publications describe the Brunswick Aquifer as primarily
having secondary porosity with the majority of the fractures and joints providing the principal
passages for groundwater flow and occurrence (Sloto et. aI., 1995). Two pumping tests have
been performed at the Site. The first evaluated the hydrologic properties of the unconsolidated
sediments while the second focused on bedrock. Neither test provided information on the
hydraulic communication between the shallow groundwater located in the unconsolidated
sediments and the saturated bedrock. Site boring logs indicate an absence of an aquiclude
between the unconsolidated sediments and the bedrock allowing for the vertical migration of
contaminants in groundwater from the unconsolidated sediments into lower bedrock units.
Cross Section A‐A’ on Figure 6a, shows the dipping siltstone units in relation to the
unconsolidated sediments. Cross Section B‐B’ on Figure 6b is constructed along the strike of the
bedrock. Cross‐Sections from the May 2009 RIR/ RASR/ RIW are included in Appendix G which
depict the vertical and horizontal fractures concluded from the October 2004 bedrock study.
For the purposes of this report, the wells associated with this Site have been grouped based on
specific characteristics. Unconfined groundwater is present in the unconsolidated sediments
and wells screened within these sediments are designated as “Unconsolidated Wells”. Wells
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screened within the siltstone bedrock are designated “Bedrock Wells”. The Bedrock Wells are
then divided into groups that intersect the same general bedding planes stratigraphically. This
division of wells is based on the premise that the Brunswick Aquifer primarily has secondary
porosity with the majority of the fractures and joints providing the principal passages for
groundwater flow and occurrence (Sloto et. aI., 1995), that fractures and partings occur along
bedding planes (Drake et aI., 1996), and “Ground water occurs along bedding surfaces, joints…”
(NJDEP, 1990).
Aquilogic assigned the groundwater zones beneath the Site the arbitrary names: Zone A,
Zone B, Zone C, and Zone D. To the northwest of the Site, a Zone Z exists above Zone A. Note:
Some wells within the same zone have differing screen intervals because the bedrock is dipping.
Those wells that extend through the boundaries of two zones and extend greater than 5 feet
into both zones have been designated as dual‐zoned (e.g. Zone B/C) accordingly. These wells
have not been used for examining groundwater gradients. Examples of the naming convention
are shown below, pictorially on cross section A‐A’ and B‐B’ (Figures 6a and 6b), and the zone
designations for each well are on Table 1.
MW‐10R – Zone A
MW‐5D – Zone B
MW‐5D2R – Zone C
MW‐5D3 – Zone D
MW‐12D – Zone B
MW‐16D – Zone B/C
Groundwater monitoring and flow information for each bedrock zone is in Section 5.3. The
anomalously high groundwater elevations from the June 8, 2010 groundwater monitoring event
were not used for analyzing average groundwater gradients. The most recent groundwater
elevation data is on Figures 7bi and 7bii.
5.2
Unconsolidated Wells
5.2.1
Depth/Elevation
The depth to water in the Unconsolidated Wells has ranged from a minimum of ~ 27 to a
maximum of ~42 feet bgs corresponding to an elevation of 286 to 300 feet AMSL (Table 2). All
of the on‐site unconsolidated wells are currently being used for remedial extraction. This wide
elevation range between wells in close proximity is likely due to a combination of seasonal
recharge variations, remediation activities, and off‐site groundwater pumping.
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5.2.2
Flow Direction and Gradient
“Groundwater flow direction in the overburden aquifer was determined to be towards the west
or northwest during the four most recent sampling events, which is consistent with historical
data.” (Kleinfelder, 2010A; SITE213‐008983) However, based on data prior to the initiation of
the groundwater extraction system in December 2004 and the use of the on‐site unconsolidated
wells as extraction wells, the groundwater in the unconsolidated sediments generally flows to
the southwest as depicted on the rose diagram, Figure 7ai. Hydraulic gradients are generally
steep between 0.067 feet/foot and 0.125 feet/foot with an average gradient of 0.092 feet/foot.
5.2.3
Hydraulic Properties
As part of a “GWP&T and SVE feasibility tests” conducted from May to June 2003, “Rising head
slug testing was conducted using MW‐1, MW‐3, and MW‐6 as the test wells. The average
hydraulic conductivity for the overburdened aquifer was calculated to be 3.805 feet per day”
(Kleinfelder, 2010B; SITE213‐009217). The average depth to water in the unconsolidated zone is
34 feet bgs (290.87 feet AMSL).
5.2.4
Velocity
Using 0.33 as a representative effective porosity (ne) for fine sand (McWorter and Sunada,
1977), the above average hydraulic gradient (i) (0.092 feet/ foott), and the calculated hydraulic
conductivity (K) (3.805 feet/day), the average linear velocity in the unconsolidated sediments is
1.06 feet/day (387 feet/year) per the equation:
V = K*i/ne
5.3
Bedrock Wells
5.3.1
Zone A Wells
5.3.1.1
Zone A Depth/Elevation
There are no on‐site Zone A monitoring wells. Two off‐site wells MW‐10R and MW‐11R are
screened within this zone. Depth to water in MW‐10R has ranged from 41.39 to 43.56 feet bgs
with a corresponding elevation of 278.40 to 280.57 feet AMSL. Depth to water in MW‐11R
ranged from 46.80 to 48.15 feet bgs with a corresponding elevation of 273.50 to 274.85 feet
AMSL.
5.3.1.2
A Zone Flow Direction and Gradient
Groundwater flow and gradient cannot be determined using the data reviewed.
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5.3.2
5.3.2.1
Zone B Wells
Zone B Depth/Elevation
On‐site extraction well MW‐5D and off‐site monitoring wells MW‐10D, MW‐11D, and MW‐12D
are screened within this zone. MW‐5D is an extraction well and has not been used in this
analysis as the field procedures used to determine the depth to groundwater in remediation
wells is unknown.
The following is the most recent data in which all three wells were measured on the same day:
MW‐10D
Date
(Feet AMSL)
12/2/2009
282.32
9/29/2009
283.12
6/11/2009
282.47
3/10/2009
281.17
5.3.2.2
MW‐11D
(Feet AMSL)
265.94
263.05
270.29
268.95
MW‐12D
(Feet AMSL)
263.53
265.64
264.70
258.16
Zone B Flow Direction and Gradient
Based on these groundwater monitoring events, the groundwater flow direction in the Zone B is
predominately toward the southwest from the Site, which is along the general strike of the
bedrock. Based on the above data, the average hydraulic gradient is steep and estimated at
0.118 feet/foot.
5.3.3
5.3.3.1
Zone C Wells
Zone C Depth/Elevation
On‐site monitoring well MW‐5D2 was replaced by well MW‐5D2R in October 2006 (Kleinfelder,
2010A; SITE213‐008972). On‐site well MW‐5D2R and off‐site wells MW‐9D and MW‐17D are
screened within Zone C.
The following is the most recent data in which all three wells were measured on the same day:
MW‐5D2R
Date
(Feet AMSL)
12/14/2010
260.35
9/15/2010
260.60
12/9/2009
264.10
9/29/2009
265.50
MW‐9D
(Feet AMSL)
275.82
274.37
274.74
273.13
MW‐17D
(Feet AMSL)
262.43
264.81
267.40
271.37
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5.3.3.2
Zone C Flow Direction and Gradient
Based on these groundwater monitoring events, the groundwater flow direction in Zone C is to
the northwest from the Site, which corresponds with the general dip of the bedrock. Based on
the above data, the average hydraulic gradient is steep and estimated at 0.080 feet/foot.
5.3.4
5.3.4.1
Zone D Wells
Zone D Depth/Elevation
On‐site groundwater monitoring well MW‐5D3 and off‐site well MW‐17D2 are the only Zone D
groundwater monitoring wells at the Site. Depth to water in MW‐5D3 has ranged from 90.79 to
119.84 feet bgs with a corresponding elevation of 205.17 to 234.22 feet AMSL. Depth to water
in MW‐17D2 ranged from 81.72 to 92.80 feet bgs with a corresponding elevation of 217.70 to
228.78 feet AMSL. The large fluctuation in groundwater elevations likely reflect pumping
activity in nearby WSWs.
5.3.4.2
Zone D Flow Direction and Gradient
Groundwater flow and gradient cannot be determined with the available data.
5.3.5
Bedrock Hydraulic Properties
The SCM prepared by Kleinfelder in 2009 states that the “current conceptual model for
groundwater beneath the Site is predominately along strike from Exxon Site #31310 to the
southwest of the site towards the Bottle King property, with a lesser flow component down dip.”
Anisotropic flow within the bedrock units is expected within this formation. Within wells
associated with this Site, average depth to groundwater increases from 54 (271 feet AMSL) to
104 feet bgs (221 Feet AMSL) between Zone B and Zone D, respectively.
In January 2007, step‐drawdown and constant‐rate pumping tests were conducted using Zone B
well MW‐5D as the extraction well and Zone B monitoring wells MW‐10D and MW‐11D and
Zone C well MW‐9D as monitoring wells. “Results of the pumping tests indicate the maximum
sustainable pumping rate for MW‐5D was 2.5 gallons per minute and that the water‐bearing
fractures in monitoring wells MW‐5D, MW‐9D and MW‐11D exhibited connectivity. Hydraulic
conductivity and specific storage for the bedrock aquifer fractures were estimated to be 0.9378
foot per day and 6.88E‐12 per foot, respectively.” (Kleinfelder, 2008; SITE213‐006564 and ‐
006565). “… constant‐rate pumping test was conducted utilizing MW‐5D as the extraction well…
Based on the results of the aquifer testing, hydraulic conductivity and specific storage for the
bedrock aquifer matrix were estimated to be 9.678E‐6 foot per day and 2.837E‐8 per foot,
respectively. Drawdown was detected in observation wells MW‐9D and MW‐11D, which
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indicates that the fractures in MW‐5D, MW‐9D and MW‐11D exhibited connectivity.”
(Kleinfelder, 2007; SITE213‐001984 and ‐001985). Based on the connectivity of MW‐5D and
MW‐11D, as determined during the January 2007 aquifer testing, groundwater flow in the Zone
B bedrock aquifer is predominately along strike to the southwest. Based on the observed water
levels during the test at MW‐5D and MW‐9D it was concluded that hydraulic connection exists
between Bedrock Zone B and C.
5.3.6
Velocity
The wells used for the calculation of the hydraulic conductivity of the bedrock are screened in
the Zone B and Zone C aquifer units. These units have different groundwater elevations,
gradients, and flow directions. Therefore, the estimated hydraulic conductivity is probably not
representative of a single hydrogeologic zone. Given that, and the anisotropic nature of fracture
dominated flow, velocity cannot be estimated based on existing information. However, it is
likely higher than that estimated for the overlying unconsolidated sediments; that is, greater
than 1 foot/day.
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6.0
CONTAMINANT CONDITIONS
6.1
Chemicals of Concern
The principle chemicals of concern (COCs) are MTBE, TBA, and benzene. It should be noted that
elevated concentrations of lead have also been detected in groundwater beneath the Site.
Groundwater analytical results are summarized in Appendix A (by well) and Appendix B (by
date). A summary of key groundwater data is illustrated on Table 5.
6.2
Soil and Soil Vapor Contamination
6.2.1
Nature
Soil sampling was limited to exploratory borings using direct push methods. All of the wells
were drilled with air‐rotary drill rigs and consequently no soil samples were collected. Soil
samples were collected during piping and tank upgrades and as part of Phase 2 divestment
activities. Soil data tables do not report fuel oxygenate results for those soil samples collected.
Soil boring locations are located on Figure 2 and Figure 2a and soil analytical data is in Appendix
D.
6.2.2
Magnitude
The data does not indicate that soil samples at the Site were analyzed for MTBE and TBA. Soil
samples were analyzed for aromatic hydrocarbons (BTEX) and a few soil samples were analyzed
for total petroleum hydrocarbons as gasoline (TPHg). The following are the maximum
concentrations of benzene and TPHg in soil samples collected as part of investigations at the
Site:
Benzene: 49.0 milligrams per kilogram (mg/kg) in a sample collected from SB‐9 at 15 to
15.5 feet bgs on December 14, 2001 (Kleinfelder, 2010A; SITE213‐009083).
TPHg: 3,540 micrograms per kilogram (mg/kg) in a sample collected from SB‐2 (2010) at
17.5 to 18.0 feet bgs (Kleinfelder, 2010A; SITE213‐009083).
Several episodes of indoor air monitoring were conducted at the private residence directly to
the south of the Site at 16 Sherbrooke Parkway. Indoor air monitoring was also conducted to
the west of the Site at the commercial building at 20 to 24 East Mount Pleasant Avenue. Copies
of soil vapor tables are in Appendix E.
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Vapor samples collected on August 5, 2004 from the private property at 16 Sherbrooke Parkway
located directly south of the Site had MTBE detections above the NJDEP Indoor Air Screening
Levels (IASLs). Again on October 14, 2004, air samples were collected from this private
residence and MTBE was detected above the IASL in the basement, basement crawl space, the
first floor and the outside of the house. A third vapor sampling event was conducted on April 21,
2005. Benzene was detected above the IASL in the basement and MTBE was detected above
the IASL in the bathroom. In a document prepared by Kleinfelder on February 23, 2011, it states
“Exceedances of the NJDEP Soil Gas Screening Levels (SGSL) were not detected in the sub‐slab
soil gas samples collected during the vapor intrusion investigation activities described above.
Because the house has an attached garage where automobiles, gasoline cans and other
potential sources of the gasoline‐related compounds detected in indoor air samples could be
present; and because exceedances of the NJDEP SGSL were not detected (in the sub‐slab
samples), ExxonMobil has not proposed further vapor intrusion investigation activities at 16
Sherbrooke Parkway” (Kleinfelder, 2011; SITE213‐008399). Results of the indoor air sampling at
16 Sherbrooke Parkway are provided in Appendix E. No additional vapor sampling has been
conducted at 16 Sherbrooke Parkway since April 2005.
Indoor Air sampling was conducted at 20 to 24 East Mount Pleasant Avenue in the commercial
buildings on October 19, 2009 and on November 19 through 21, 2009. Benzene was detected at
levels exceeding the IASL. TCE and PCE were also detected, and these chlorinated solvents are
not typically associated with gasoline contamination. The NJDEP required ExxonMobil to
conduct an investigation in the vicinity of the auto repair shop to determine if a source for the
TCE and PCE was at the Site. No source at the Site was located (Kleinfelder, 2011; SITE213‐
008401). No additional vapor sampling has been conducted at 20 to 24 East Mount Pleasant
Avenue.
In April 2006, the NJDEP Bureau of Emergency Response responded to a request for assistance
when 50% LEL readings were detected in Bell fiber optic cable boxes approximately 40 feet to
the northwest of MW‐4 (NJDEP Bureau of Emergency Response Region I, 2011; SITE213‐008383
to ‐008388).
6.2.3
Extent
The magnitude and extent of MTBE and TBA within the vadose zone beneath the Site appears to
not have been investigated. No analytical data for these constituents has been included in any
soil data tables associated with site reports; therefore, the extent of contamination cannot be
determined.
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Benzene: In January 2003, benzene was detected in a saturated soil sample collected from
34.0 to 34.5 feet bgs (SB‐20) at a concentration of 2.01 mg/kg. This is the deepest soil
sample collected at the Site and indicated that benzene contamination in soil extended to
groundwater in 2003. The maximum concentration of benzene detected at the Site (49.0
mg/kg) was from SB‐9 at a depth of 15 to 15.5 feet bgs. A more recent boring SB‐2 (2010)
was drilled in February of 2010 and was located 15 feet south of SB‐9. SB‐2 (2010) had the
second highest concentration of benzene ever detected at the Site with a concentration of
45.5 mg/kg at a depth of 17.5 to 18. From this data, benzene contamination is currently
present to the east of the current Site USTs to at least 18 feet bgs. Another boring SB‐1
(2010) which was also drilled recently, but to the west of the current USTs, had a benzene
concentration of 11.8 mg/kg (16.5 to 17 feet bgs). This data indicates that benzene is also
present to at least 17 feet to the west of the current USTs. Currently, benzene is not
delineated laterally in soil and likely still extends to groundwater at the Site.
TPHg: Only samples collected from piping and dispenser island upgrades, and the most
recent borings SB‐1 (2010) through SB‐6 (2010), were tested for TPHg. TPHg was detected
in SB‐1 (2010), SB‐2 (2010), and SB‐3 (2010) from 17 to 20 feet bgs. From this data, it
appears that TPHg contamination currently exists in the vicinity of former and current USTs
to at least 20 feet bgs, and extends to groundwater. Currently, TPHg is not delineated
vertically and laterally at the Site.
6.3
LNAPL
6.3.1
Nature
LNAPL was measured in unconsolidated sediment groundwater monitoring wells immediately
after installation in January 2002 and persisted until September 2007.
6.3.2
Magnitude
A maximum LNAPL thickness of 1.18 feet was observed at on‐site monitoring well MW‐4 on
April 4, 2003 (Geologic Services Corporation, 2004A; SITE213‐001131).
6.3.3
Extent
LNAPL was measured in MW‐1, MW‐2, MW‐4, and MW‐7 and once in MW‐6. The majority of
the LNAPL plume has been in the eastern half of the Site in the vicinity of at least three
generations of USTs. There have been no dedicated unconsolidated sediment groundwater
monitoring wells at the Site since July 2004 (all wells are connected to the on‐site remediation
system) and no unconsolidated sediment wells installed off‐site down‐gradient of the Site.
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“(Liquid phase hydrocarbon) LPH bailing events were conducted from May 6, 2003 through
February 2004 and approximately 354 gallons of groundwater and LPH were recovered.”
(Kleinfelder, 2008; SITE213‐006565). A total of 198.5 gallons of LNAPL were removed from well
MW‐4 alone which is located in the northeastern area of the Site. All wells that contained LNAPL
are now connected to the remediation system. LNAPL has not been detected in any bedrock
wells; however, no bedrock wells have been installed on the eastern half of the site near the
USTs.
6.4
Groundwater Contamination
6.4.1
Nature
Petroleum hydrocarbon impacts to groundwater were detected with the installations of the first
wells in January of 2002. Contaminant concentrations at on‐site wells have diminished over time
as a result of on‐site remediation and off‐site contaminant migration. MTBE analytical results
are shown on Figures 8a, 8b, and 8d and TBA analytical results are on Figures 9a, 9b, and 9d.
Time‐Series Hydrographs for each well are provided in Appendix C.
6.4.2
6.4.2.1
Magnitude
Unconsolidated Sediment Wells
Benzene
●
Initial: Benzene was first detected at a concentration of 39,400 µg/L in a sample collected
from MW‐1 on January 29, 2002. MW‐1 is located to the northeast of the USTs.
●
Maximum: The maximum historic detection of benzene in unconsolidated groundwater was
46,400 µg/L in a sample collected from MW‐1 on September 3, 2003.
●
Current: Remediation wells MW‐2 through MW‐4 were not sampled during the most recent
sampling event for which we have data (December 2010). However, using the sampling
data from September 2010 and December 2010, the maximum detection of benzene in
unconsolidated groundwater was 510 µg/L in a sample collected from MW‐3. MW‐3 is
located to the west of the dispenser island near the northern property line.
MTBE
●
Initial: MTBE was first detected at a concentration of 187,000 µg/L in a sample collected
from MW‐2 on January 29, 2002. MW‐2 is located south of the current operating USTs near
the southern property line.
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●
Maximum: The maximum historic detection of MTBE in unconsolidated groundwater was
234,000 µg/L in a sample collected from MW‐1 on July 1, 2003. MW‐1 is located to the
northeast of the current operating tanks.
●
Current: The maximum detection of MTBE in unconsolidated groundwater during the most
recent sampling event for which we have data (December 2010) was 98.4 µg/L in a sample
collected from MW‐1. MW‐1 is located to the northeast of the current operating tanks.
TBA
●
Initial: TBA was first detected at a concentration of 80,100 µg/L in a sample collected from
MW‐2 on January 29, 2002. MW‐2 is located south of the current operating USTs near the
southern property line.
●
Maximum: TBA was detected at a maximum concentration of 118,000 µg/L in a sample
collected from unconsolidated sediment monitoring well MW‐2 on July 11, 2002. MW‐2 is
located south of the current operating USTs near the southern property line.
●
Current: The maximum detection of TBA in unconsolidated groundwater during the most
recent sampling event for which we have data (December 2010) was 2,990 µg/L in a sample
collected from MW‐1. MW‐1 is located to the northeast of the current operating tanks.
6.4.2.2
Bedrock Wells
Benzene
●
Initial: MTBE was first detected in bedrock groundwater at a concentration of 3,370 µg/L in
a sample collected from on‐site well MW‐5D on July 1, 2003. Well MW‐5 is located near the
western property line.
●
Maximum: The maximum historic detection of benzene in bedrock groundwater was 5,970
µg/L in a sample collected from MW‐5D on June 9, 2004.
●
Current: The maximum detection of benzene in bedrock groundwater during the most
recent sampling event for which we have data (December 2010) was 308 µg/L in a sample
collected from MW‐5D.
MTBE
●
Initial: MTBE was first detected in bedrock groundwater at a concentration of 21,000 µg/L
in a sample collected from MW‐5D on July 1, 2003.
●
Maximum: The maximum historic detection of MTBE in bedrock groundwater was 33,700
µg/L in a sample collected from MW‐5D on June 9, 2004.
●
Current: The maximum detection of MTBE in bedrock groundwater during the most recent
sampling event for which we have data (December 2010) was 195 µg/L in a sample collected
from MW‐16D. Well MW‐16D is located 250 feet southwest of the property line.
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TBA
●
Initial: TBA was first detected in bedrock groundwater at a concentration of 10,700 µg/L in a
sample collected from MW‐5D on July 1, 2003.
●
Maximum: The maximum historic detection of TBA in bedrock groundwater was also 24,200
µg/L in a sample collected from MW‐5D on July 14, 2003.
●
Current: The maximum detection of TBA in bedrock groundwater during the most recent
sampling events for which we have data (December 2010) was 5,350 µg/L in a sample
collected from MW‐5D.
6.4.3
6.4.3.1
Extent
Unconsolidated Sediments
Unconsolidated sediment groundwater monitoring well MW‐10 only contained enough water to
sample on three occasions and MW‐11 was dry for all sampling events. These wells were
re‐drilled entirely into shallow bedrock as MW‐10R and MW‐11R and are now considered
Zone A bedrock monitoring wells based on the lithology recorded on the boring logs.
Benzene
Benzene has been detected in groundwater samples collected from unconsolidated monitoring
wells MW‐1 through MW‐9. There are no off‐site, down‐gradient unconsolidated sediment
monitoring wells. Wells MW‐1 through MW‐8 were converted to remediation extraction wells.
In the unconsolidated sediments, the groundwater flow is to the southwest. Therefore, benzene
is delineated up‐gradient by unconsolidated groundwater monitoring wells MW‐14S and MW‐9
and delineated cross‐gradient (to the south) by MW‐13 and cross‐gradient to the west by
MW‐15. No off‐site groundwater monitoring wells screened within the unconsolidated
sediments have been installed to the southwest of MW‐7 and MW‐8; therefore, the lateral
extent of benzene contamination is not delineated down‐gradient of the Site.
MTBE
MTBE has been detected in unconsolidated sediment groundwater samples collected from wells
MW‐1 through MW‐8 and MW‐13. Wells MW‐1 through MW‐8 are located on‐site and MW‐13
cross‐gradient to the south of the Site. Wells MW‐1 through MW‐8 were converted to
remediation extraction wells. MTBE was not detected in MW‐9 above the estimated value of
0.42 µg/L and was not detected in MW‐14S and MW‐15S. Groundwater flows to the southwest
in the unconsolidated sediments and MTBE was delineated in the unconsolidated groundwater
up‐gradient (to the north) by MW‐14S and cross‐gradient (to the west) by MW‐15S. The
maximum MTBE detected in MW‐13 has been 4.1 µg/L (3/21/2006), reasonably delineating
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MTBE contamination cross‐gradient (to the south). No groundwater monitoring wells screened
within the unconsolidated sediments have been installed to the southwest of MW‐7 and MW‐8;
therefore, the lateral extent of MTBE contamination is not delineated down‐gradient of the Site.
TBA
TBA has been detected in unconsolidated sediment groundwater samples collected from wells
MW‐1 through MW‐8. Wells MW‐1 through MW‐8 are located on the Site; however, these
wells were converted to remediation extraction wells. TBA was not detected in MW‐9, MW‐13,
MW‐14S, and MW‐15S. Groundwater flows to the southwest in the unconsolidated sediments
and TBA was delineated in the unconsolidated groundwater up‐gradient (to the north) by
MW‐14S, and cross‐gradient (to the west) by MW‐15S. The maximum TBA detected in MW‐13
has been 4.1 µg/L (3/21/2006), reasonably delineating TBA contamination cross‐gradient (to the
south). No groundwater monitoring wells screened within the unconsolidated sediments have
been installed to the southwest of MW‐7 and MW‐8; therefore, the lateral extent of TBA
contamination is not delineated down‐gradient of the Site.
6.4.3.2
Bedrock
Bedrock Zone A
Two wells have been installed into the uppermost Bedrock Zone A, off‐site wells MW‐10R and
MW‐11R. Groundwater flow in this zone cannot be estimated; however, it is likely to the
southwest. Benzene, MTBE, and TBA have been detected in both wells. Current benzene
concentrations are 268 µg/L in MW‐10R and 138 µg/L in MW‐11R. MTBE is currently not
detected in MW‐10R and is 26.7 µg/L in MW‐11R. Current TBA concentrations are 168 µg/L in
MW‐10R and 462 µg/L in MW‐11R. In Zone A, benzene, MTBE, and TBA contamination is
currently at least 170 feet off‐site to the southwest and is not delineated in this direction.
Bedrock Zone B
Four wells have been installed into Bedrock Zone B, on‐site well MW‐5D and off‐site wells
MW‐10D, MW‐11D, and MW‐12D. Benzene has been detected in all wells except MW‐12D. The
maximum current detection in this zone is 180 feet to the southwest of the Site. Groundwater in
Zone B flows predominately to the southwest and appears to be delineated cross‐gradient to
the northwest by MW‐12D; however, the benzene contamination is not delineated up‐gradient
to the northeast, cross‐gradient to the southeast, or down‐gradient to the southwest. In Zone B,
benzene is currently at least 170 feet off‐site to the southwest (MW‐11D).
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MTBE has been detected in all wells and is not delineated in any direction. In Zone B, MTBE
contamination is currently at least 270 feet off‐site to the northwest (MW‐12D) and 170 feet off‐
site to the southwest (MW‐11D).
TBA has been detected in all wells; however, during the last sampling of MW‐10D in September
of 2010, TBA was not detected. During the June 2010 sampling event, TBA was detected at
538 µg/L at MW‐10D. TBA contamination is not delineated in any direction in Bedrock Zone B. In
Zone B, TBA is currently at least 270 feet off‐site to the northwest (MW‐12D) and 170 feet off‐
site to the southwest (MW‐11D).
Bedrock Zone B/C
Two off‐site wells have been installed with screens that extend into both Zones B and C.
MW‐14D is located 320 feet up‐gradient to the northeast, and benzene, MTBE, or TBA have not
been detected at this well. MW‐16D is located 250 feet southwest of the Site, and benzene,
MTBE, and TBA concentrations of 26.5, 195, 726 µg/L , respectively, have been detected at this
well. In Bedrock Zone B/C, benzene, MTBE, and TBA contamination extends at least 250 feet
southwest of the Site. Former Livingston Manor well LMW‐2 was screened within the Zone B
and C and benzene, MTBE, and TBA concentrations were detected at this well. If this data is
taken into consideration, it can be inferred that these COCs also extend at least 400 feet to the
northwest of the Site.
Bedrock Zone C
Four wells have been installed into Bedrock Zone C, on‐site former well MW‐5D2 and
replacement well MW‐5D2R, and off‐site wells MW‐9D and MW‐17D. Benzene, MTBE, and TBA
have been detected at both MW‐5D2 and MW‐5D2R. Benzene and TBA, and only low
concentrations of MTBE have been detected at MW‐9D. Historically, benzene has not been
detected at MW‐17D, but MTBE and TBA have been detected up to 124 µg/L and 47 µg/L,
respectively. TBA was not detected and MTBE concentrations were low at MW‐17D during the
most recent groundwater sampling event in December of 2010. Groundwater in Zone C flows
predominately to the northwest and appears to be delineated up‐gradient to the east by MW‐
9D and cross‐gradient to the southwest by MW‐17D. No wells screened within Zone C have
been installed off‐site to the northwest down‐gradient of MW‐5D2R; therefore, the lateral
extent of contamination to the northwest is not delineated. However, Livingston Manor well
LMW‐3 which was screened into Zone C, can be used to infer that benzene, MTBE, and TBA
extended at least 300 feet to the northwest of the Site in 2004.
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Bedrock Zone D
Two wells have been installed into Bedrock Zone D, on‐site well MW‐5D3 and off‐site wells MW‐
17D2. Low MTBE concentrations and no TBA has been detected at MW‐5D3. However, this well
had maximum detections of 512 µg/L MTBE and 411 µg/L TBA in October of 2005. Benzene,
MTBE, and TBA have been not been detected in MW‐17D2. Groundwater flow direction in this
zone cannot be determined, and the extent of contamination is unknown.
6.4.3.3
Summary of Plume Dimensions
Benzene
The data suggests that the benzene plume is limited to the Unconsolidated Zone groundwater
and bedrock groundwater in Zone A and B, with the exception being Zone B/C at Well MW‐16D.
This plume measures at least 250 feet long to the southwest (MW‐16D) by 120 feet wide, with a
depth of approximately 70 feet bgs at MW‐16D (the bottom of the MW‐16D well screen).
MTBE
The data indicates that the MTBE plume extends from the on‐site Unconsolidated Zone to the
southwest, and to the southwest and northwest along strike and dip of the various bedrock
units. MTBE has been detected in the deepest on‐site well installed to date (MW‐5D3) and has
been detected down strike in a southwesterly direction in Zone A, B, B/C, and C wells to the
most distant well installed from the Site (MW‐17D). MTBE contamination does not appear to
extend along strike to the depth of the Zone D groundwater at MW‐17D2. Based on this data
the plume extends at least 460 feet down strike (southwest) to a depth of at least 70 feet bgs.
The predominant groundwater flow direction is down dip to the northwest of the Site in Zone C.
MTBE is not delineated down‐gradient of Zone C well MW‐5D2R. However, Zone B well MW‐12D
has MTBE contamination. Based on this data, the plume extends at least 270 feet to the
northwest to a depth of at least 101 feet bgs (the bottom of the screen interval for MW‐12D). If
the data collected from Former Livingston Manor wells are taken into consideration, the MTBE
plume in 2004 extended at least 400 feet to the northwest of the Site to a depth of 141 feet bgs
(bottom of screened interval for LMW‐3).
TBA
Historically, the TBA plume has similar dimensions to the MTBE plume extending to at least 460
feet down strike to the southwest and to a depth of 70 feet bgs. Currently, TBA contamination
extends at least 250 feet down strike (southwest) to the most distal well MW‐16D (726 µg/L).
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The predominant groundwater flow direction is down dip to the northwest of the Site in Zone C,
and TBA is not delineated down‐gradient of Zone C well MW‐5D2R. However, Zone B well
MW‐12D has TBA contamination. Based on this data, the plume extends at least 270 feet to the
northwest to a depth of at least 101 feet bgs (the bottom of the screen interval for MW‐12D). If
the data collected from Former Livingston Manor wells are taken into consideration, the TBA
plume in 2004 extended at least 400 feet to the northwest of the Site to a depth of 141 feet bgs
(bottom of screened interval for LMW‐3).
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7.0
REMEDIATION
Remediation at the Site has consisted of soil excavation, bailing events to remove LNAPL, SVE,
and GWP&T, as discussed below. According to available reports, all remediation activities had
only occurred on‐site as of December 2010.
In October 1986, “Approximately five tons of soil and 765 gallons of liquid were disposed of
during the UST removal activities.” (Kleinfelder, 2010B; SITE213‐009217).
In May 2001, a drive‐off at a dispenser discharged less than a gallon of gasoline to the
pavement and to the pea gravel beneath the dispenser island. In November of the same
year, approximately one ton of pea gravel was removed from around a gasoline flex line and
hauled off‐site for disposal (Kleinfelder, 2010B; SITE213‐009217).
“LPH bailing events were conducted from May 6, 2003 through February 2004 and
approximately 354 gallons of groundwater and LPH were recovered.” (Kleinfelder, 2008;
SITE213‐006565).
In March 2004, five previously abandoned‐in‐place USTs and the associated product piping
were removed (Geologic Services Corporation, 2004B; SITE213‐000403 and ‐000404). “135
tons of soil were removed from the site.” (Kleinfelder, 2008; SITE213‐006565).
In May and June 2003, GWP&T and SVE feasibility tests were conducted to evaluate the
effectiveness of GWP&T and SVE as remedial technologies for the Site (Kleinfelder, 2010A;
SITE213‐008970). “These results indicate that a GWPT/SVE system would be effective at
remediating and inhibiting the migration of dissolved phase hydrocarbon downgradient of
the dispenser island and UST area. Based on test data, an effective radius of influence (ROI)
for SVE system is estimated at 45 feet at an applied vacuum of 55 inches of water. In
addition, groundwater recovery and observed drawdown data indicates a groundwater
capture ROI of approximately 51 feet which is anticipated to be sufficient to inhibit off site
migration.” Based on this data, an extraction well network was constructed using the
existing groundwater monitoring wells MW‐1 through MW‐8. Monitoring wells MW‐5D and
MW‐5D2 were added to the remedial system piping layout due to “recent groundwater
concentrations, and initially will not be hooked up to the GWPT/SVE system, but are added
for potential future use.” (Geologic Services Corporation, 2004A; SITE213‐001102).
The SVE system was installed and started in July 2004 extracting from on‐site
unconsolidated groundwater monitoring wells MW‐1 through MW‐8. The SVE system was
shut down in November with the failure of the catalytic‐oxidation unit. These wells were
screened from an average of 22 to 42 feet bgs with the average depth to water at
approximately 33 feet bgs. The SVE system has operated through at least December 2010
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according to the last available information, and a total of 12,475 pounds of hydrocarbons
had been removed as of September 2010. No additional vapor extraction wells were
installed at the Site.
In December 2004, The GWP&T system was activated utilizing eight groundwater
monitoring wells, MW‐1 through MW‐8, as extraction wells at a maximum pumping rate of
two gallons per minute (Kleinfelder, 2010A; SITE213‐008971). Groundwater is recovered
from MW‐1 through MW‐8 utilizing submersible pumps. The catalytic‐oxidation unit was
replaced in January 2005 and the system restarted (Kleinfelder, 2008; SITE213‐006563).
“Active remediation of the bedrock aquifer did not begin until May 2007, when monitoring
well MW‐5D was connected to the GWP&T system as an extraction well for the shallow
bedrock aquifer.”(Kleinfelder, 2010A; SITE213‐008992). However, an e‐mail dated
November 28, 2007 from Gary A. Slater (NJDEP) asked William E. Gottobrio (Kleinfelder) if
they had begun “pumping from 5D yet?” Gottobrio responded that they had “been pumping
from MW‐5D since November 8, 2007” (Gottobrio, 2007; SITE213‐008558). As of September
2010, the GWP&T system has removed 191 pounds of dissolved phase hydrocarbon and
1,311,183 gallons of groundwater. “The dissolved phase hydrocarbon recovery trend for the
GWP&T system indicates that hydrocarbon mass recovery has not reached asymptotic
conditions”. (Kleinfelder, 2010A; SITE213‐008985 to ‐008987).
“During UST system upgrade activities conducted in April 2006, 122.33 tons of soils were
removed from the site.” (Kleinfelder, 2008; SITE213‐006565)
A Site Status Update was prepared by ExxonMobil in January of 2011, “Assuming approval of
the September 2010 Remedial Action Workplan Addendum (RAWA) by the New Jersey
Department of Environmental Protection (NJDEP), the MW‐10 and MW‐11 cluster wells are
expected to be brought on‐line with the existing onsite remedial system in the first quarter of
2011” (ExxonMobil, 2011; SITE213‐008524). No additional information was obtained.
As of December 2010, on‐site SVE and on‐site GWP&T had been operating at the Site for
approximately six years, and had not reached asymptotic levels. The on‐site remedial activities
were not designed to address the complete lateral and vertical extent of the hydrocarbon and
fuel oxygenate detections in soil and groundwater. As of December of 2010, no off‐site
remediation had been conducted to contain and mitigate contaminant migration off‐site and at
depth.
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8.0
FATE AND TRANSPORT
8.1
Physical and Chemical Properties of COCs
The environmental fate and transport of benzene, MTBE and TBA in groundwater at the Site can
be estimated from the release histories at the source site(s), the hydrogeology and groundwater
flow conditions beneath the source site(s), and the chemical properties of these constituents
(Table 4).
The aqueous solubility of the constituents at their respective volume in gasoline will determine
their partitioning into groundwater after a release; that is, the rate at which dissolution will
occur and the resulting magnitude of the contaminant concentration in groundwater. MTBE
and TBA are considerably more soluble than benzene. Benzene is the least soluble constituent.
In addition, unleaded gasoline generally contains between 0.12% and 3.5% benzene and 11%
and 15% MTBE (for oxygenated gasoline) (State of California, 1988; Chevron, 1993). Therefore,
the mole fraction solubility for MTBE versus benzene will be even higher than the aqueous
solubility. Given this, one would expect MTBE to dissolve in groundwater much faster than the
other constituents and be present at much higher dissolved concentrations, followed by TBA.
Dispersion will tend to spread the contaminants within the aquifers in the transverse,
longitudinal, and vertical directions. This results in dilution of the contamination, but
longitudinal dispersion also allows some contaminant to migrate faster than the average
velocity. However, various physical and chemical processes can act to slow the movement and
reduce the concentration of these constituents in groundwater. The combination of all of these
processes is commonly referred to as chemical attenuation. Attenuation of benzene, TBA, and
MTBE in groundwater is controlled primarily by three processes: adsorption, volatilization, and
biological degradation.
Among the COCs, benzene is expected to be attenuated more strongly by adsorption relative to
MTBE and TBA. MTBE and TBA are commonly considered to be unaffected by adsorption,
possessing a partitioning coefficient that is three to six times lower than benzene. Thus, MTBE
and TBA migration normally occurs at approximately the same speed as groundwater.
All of the contaminants are susceptible to attenuation by volatilization from the water table
(controlled by the Henry’s constant). However, this volatilization will not have a significant
effect on contaminant migration in groundwater. Benzene is the most susceptible to
volatilization.
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All of the contaminants are known to undergo biological degradation under certain conditions.
Benzene is known to undergo biological degradation in groundwater under aerobic (oxygen‐
rich) and anaerobic (oxygen‐poor) conditions. TBA and MTBE are primarily susceptible to
biological decay under aerobic conditions. However, they degrade at rates three to five times
slower than benzene (Howard, 1991).
Based on the aforementioned summary of fate and transport properties, it is expected that
MTBE and TBA should move without significant attenuation within the groundwater. MTBE
would also be present at relatively high concentrations and persist longer. Benzene is the most
attenuated of these constituents and therefore, would migrate slower than MTBE in
groundwater. This observation appears to be supported by the occurrence and distribution of
COCs in groundwater beneath the Site.
8.2
Sources
The following sources of petroleum hydrocarbon contamination, including MTBE and TBA, were
identified from the data reviewed. Based on the timing of these referenced releases, they are
likely to have contained MTBE. No off‐site sources of petroleum hydrocarbon contamination
have been identified.
In May 2001, a drive‐off at the regular dispenser occurred at the Site. “Less than one gallon
of gasoline was discharged to the pavement and to the pea gravel beneath the dispenser
island. The NJDEP was notified and case # 01‐05‐04‐1325‐59 was assigned to the Site”
(Kleinfelder, 2010A; SITE213‐008969). The NJDEP Communication Center Notification Report
noted a customer drive‐off and a resulting spill of an unknown quantity and the presence of
soil contamination.
In November 2001, a release of unknown quantity was reported when the 8,000‐gallon
gasoline UST was found to be leaking. Case # 01‐11‐13‐0846‐55 (McCusker et al., 2005;
SITE213‐008513) was assigned. Repairs were conducted on the flex line for the 10,000‐
gallon UST. Approximately one ton of pea gravel was removed from around the flex line and
hauled off‐site for disposal (Kleinfelder, 2010A; SITE213‐008969).
In May 2004, a field violation was issued noting: “inaccurate registration”, “liquid/free
product in spill bucket”, and “Other: Delivery Ban. Do not fill tanks…Contaminated soil
found… run enhanced tracer test for UST system.” (McCusker et al., 2005; SITE213‐008522)
In December 2004, a drive‐off at a dispenser and a 5‐gallon release occurred at the Site. The
NJDEP was notified and case # 04‐ 12‐15‐1558‐52 was assigned (Kleinfelder, 2010A; SITE213‐
008971).
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In April 2006, UST system upgrade activities were conducted, including replacement of the
dispensers and product piping to the top of the USTs. A total of 122.33 tons of soil were
removed from the Site.
Concentrations of MTBE detected in wells (and LNAPL volumes) during the initial sampling of
MW‐1 through MW‐3 sampling on January 29, 2002 were inconsistent with the initial reported
release of 1‐gallon of gasoline. Therefore, it is likely that at least one undocumented release of
RFG had occurred at the Site prior to the sampling on January 29, 2002. In addition, there is
evidence of a much older release of leaded gasoline, as a groundwater sample from MW‐4 in
March of 2010 contained 14.9 µg/L of lead.
8.3
Pathways
Petroleum hydrocarbons, including MTBE and TBA, were released at the Site and impacted the
vadose zone in the vicinity of the current and former USTs. Given the depth to groundwater and
permeable unconsolidated sediments beneath the Site, releases rapidly entered the
unconsolidated groundwater zone. This contaminated groundwater migrated down‐gradient to
the southwest in the unconsolidated sediments towards the commercial well located at 19
South Livingston Avenue.
Contamination from the vadose zone and the unconsolidated groundwater has resulted in
detections of COCs in soil vapor. Soil vapor contamination has migrated to nearby utility man
holes/vaults and caused indoor vapor intrusion issues. Periodically, the subsurface utilities
surrounding the Site have had detections of COCs. Indoor vapor intrusion and vapor migration
studies have detected contaminants at the adjacent properties.
A downward vertical hydraulic gradient exists in the vicinity of the Site resulting from recharge
and the regional pumping of bedrock aquifers. There is also no aquitard between the
unconsolidated sediments and the bedrock beneath the site. Therefore, contaminated
groundwater in unconsolidated sediments migrates into the bedrock aquifer and flows through
fractures in the bedrock zones. Fractures within the bedrock include both sub‐vertical high‐angle
fractures and low‐angle fractures/ partings along bedding planes. In addition, former “leaking”
well MW‐5D2 could have provided a vertical pathway for contaminant migration into deeper
aquifer zones. Pumping tests utilizing a Bedrock Zone B extraction well and Bedrock Zone B and
Zone C monitoring wells established that the Bedrock Zones B and C exhibited hydraulic
connectivity.
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Groundwater flow within the vertical to orthogonal bedrock fractured zones appears to be
predominately along ‐strike (southwest) in the siltstones in the upper bedrock units (Zones A
and B) and down‐dip (northwest) along the bedding plane fractures/partings in the lower
bedrock units (Zones C and D). Therefore, the groundwater in the upper bedrock units flows
along‐strike (southwest) towards the commercial well at 19 South Livingston Avenue (Bottle
King); whereas, the groundwater in the lower bedrock units flows down‐dip (northwest)
towards Livingston PSW #11.
8.4
Receptors
Releases at the Site have contaminated groundwater resources, which constitute a receptor. In
addition, the following additional receptors are threatened or impacted:
nearby residents, building occupants, and utility workers through vapor intrusion; and
WSWs both domestic and public.
COCs have been detected at subsurface utilities and in indoor air samples at adjacent
properties. The private residence at 16 Sherbrooke Parkway has not been monitored since April
of 2005. There is no indication that additional private residences to the south have been
monitored for vapor intrusion. Benzene has been detected in indoor air samples at commercial
properties at 20 – 24 East Mount Pleasant Avenue located directly west of the Site. In April of
2006, 50% LEL readings were reported in Bell fiber optic cable boxes just north of the site.
The analysis of impacts to groundwater from MTBE released at the Site has been limited by the
Court to a delineated area in order to efficiently present evidence. Contamination released at
the Site will continue to migrate with groundwater and, without remediation, the contamination
may migrate beyond the delineation boundaries.
There is a Livingston Township PSW and two commercial/domestic supply wells well near the
Site (Figure 1). Of these WSWs, two are known to be contaminated with MTBE (Table 3). On
October 28, 2004, a maximum MTBE concentration of 13.9 µg/L was detected at the nearby
commercial supply well at 19 South Livingston Avenue. This commercial supply well is located
approximately 700 feet southwest and down‐gradient (i.e., Unconsolidated Zone and Bedrock
Zone B) of the Site. On November 19, 2009, MTBE was detected at a maximum concentration of
28.7 µg/L in Livingston PSW #11. Livingston Township Well # 11 is located approximately 1,750
feet to the northwest and down‐gradient (i.e., Bedrock Zone C and D) of the Site.
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8.5
Site Conceptual Model
8.5.1
Hydrogeology
The Site is underlain by unconsolidated sediment to a depth up to 45 feet bgs. Groundwater in
these sediments is present at an average elevation of 291 feet AMSL (approximately 36 feet
bgs). Siltstone bedrock units underlie the unconsolidated sediments with a strike of northeast‐
southwest and dip to the northwest between 7 and 14°. The Siltstone bedrock contains both
high‐angled fractures and fractures along bedding planes. The average groundwater elevation
decreases with increasing depth from an average of 271 (Zone B) to 221 (Zone D) feet AMSL.
This indicates a high downward vertical gradient likely due to recharge and regional pumping.
Groundwater flows to the southwest in the unconsolidated sediments and upper bedrock units,
and to the northwest in the lower bedrock units. See Section 5.0.
8.5.2
Releases
The Site is reported to have operated as a gasoline service station since 1934. During the long
history of Site operations, there were no reported releases of gasoline until May 2001 when
1‐gallon of reformulated gasoline was reported to have been spilled. The magnitude and
distribution of groundwater contamination in 2002 indicates that a larger release of gasoline
containing MTBE occurred prior to 2002. See Section 8.2.
8.5.3
Investigation and Remediation
Since early 2002, a total of 14 unconsolidated sediment and 16 bedrock groundwater
monitoring wells have been installed in association with this Site. All the unconsolidated
sediment wells on‐site have been converted to remediation wells and no down‐gradient wells
have been installed in unconsolidated sediments. Contaminated groundwater in the bedrock
aquifer is not delineated to the southwest and northwest.
A SVE system began operation in July 2004 extracting from on‐site unconsolidated monitoring
wells MW‐1 through MW‐8. As of December 2010, a total of 12,475 pounds of hydrocarbons
were removed using this system. A P& T system began operation in December 2004 using MW‐1
through MW‐8 and MW‐5D. As of December 2010, approximately 191 pounds of dissolved
phase hydrocarbons and 1,311,183 gallons of groundwater were removed. As of December
2010, asymtopic concentrations have not been achieved with the P&T system, and no off‐site
remediation has been conducted at the Site.
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8.5.4
COC Magnitude and Extent
The lateral and vertical extent of COCs in vadose zone soil beneath the Site has not been fully
investigated. There has been no analysis for MTBE or TBA in soil samples.
The maximum historic detection of MTBE in unconsolidated groundwater was 234,000 µg/L in a
sample collected from MW‐1 on July 1, 2003. The maximum historic detection of MTBE in
bedrock groundwater was 33,700 µg/L in a sample collected from MW‐5D on June 9, 2004.
Given the historically high MTBE concentrations on‐site (up to three orders of magnitude
greater than current MTBE concentrations), the MTBE plume likely extends off‐site and down‐
gradient (southwest) of the Site within the unconsolidated groundwater. No unconsolidated
groundwater monitoring wells have been installed down‐gradient of the Site; therefore, the
extent of MTBE contaminated groundwater within the unconsolidated sediments is unknown.
MTBE has migrated vertically on‐site in the groundwater to Bedrock Zones B, C, and D, and off‐
site to Bedrock Zones A, B, and C. MTBE has also migrated off‐site to the southwest along‐strike
of the bedrock (Zone B) and down‐dip to the northwest (Zone C). The MTBE plume is at least
600 feet long (southwest), 300 feet wide (northwest), and 121 feet deep. The majority of the
MTBE mass, as determined by observed concentrations, is currently present down‐gradient of
the Site and vertically distributed in all of groundwater Bedrock Zones. The full vertical and
horizontal extent of MTBE contamination in bedrock is unknown. See Section 6.0.
8.5.5
Pathways
COCs migrated from vadose zone soils rapidly into groundwater in the unconsolidated
sediments. COCs then migrated off‐site in the unconsolidated groundwater to the southwest.
Under the downward vertical hydraulic gradient, groundwater contamination migrated
vertically from unconsolidated sediments into the bedrock aquifer zones (A, B, C, and D).
Contaminated groundwater flows within fractures to the southwest in bedrock Zones A and B
and to the northwest in Zones C and D. See Section 8.3.
8.5.6
Receptors
COCs have been detected at subsurface utilities and in indoor air samples at adjacent
properties. MTBE concentrations have been detected at the commercial supply well at 19 South
Livingston Avenue (700 feet to the southwest) and Livingston Township PSW #11 (1,750 feet to
the northwest). See Section 8.4.
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8.5.7
Summary
COCs were released at the Site prior to 2002 and quickly migrated to groundwater in the
unconsolidated sediments beneath the Site. Contamination migrated off‐site down‐gradient to
the southwest in the groundwater in unconsolidated sediments, and within the fractured
bedrock to the southwest and northwest. The extent of contamination in groundwater has not
been delineated in the unconsolidated sediments nor in the bedrock. The neighboring
properties to the south and west of the Site have had vapor intrusion of COCs above indoor‐air
screening levels. MTBE has been detected at the commercial supply well at 19 South Livingston
Avenue and Livingston PSW #11. A SVE system and a groundwater P&T system have operated
on the Site; however, asymptotic concentrations have not been reached. No off‐site
remediation activities have been conducted to mitigate off‐site contamination.
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9.0
DATA GAPS
The following section describes data gaps and recommendations for additional Site assessment
and remediation, based on the information reviewed.
9.1
Hydrogeology
A fracture lineament assessment is needed to identify zones of increased fracture density,
and fracture orientation and depth. These features act as primary groundwater (and
contaminant) transport pathways.
Too few monitoring wells have been installed discretely in Bedrock Zones A through D to
accurately evaluate the hydraulic conditions beneath the Site and off‐site. Additional
discretely screened bedrock wells need to be installed to characterize hydrogeologic
conditions in the bedrock aquifer.
No pumping tests were conducted to evaluate hydraulic properties in the various
hydrogeologic units, and the hydraulic connectivity between specific bedrock zones and
between the unconsolidated sediments and the bedrock. Aquifer testing must be
conducted at the Site using wells that are discretely screened in specific hydrogeologic
zones.
9.2
Contamination
9.2.1
Soil and Soil Vapor
The lateral and vertical extent of petroleum hydrocarbons and fuel oxygenates in soil has
not been fully investigated. No analysis of soil samples for MTBE and TBA was identified.
Additional soil sampling should be conducted on‐site to determine if residual contaminant
mass remains in the vadose zone.
The potential health risks to building occupants, residents, and utility workers posed by soil
vapor intrusion into the service station building, the adjacent properties, and utility
manholes have not been fully investigated. Additional vapor intrusion studies should be
conducted at the neighboring properties.
9.2.2
Groundwater
The magnitude and extent of COCs in groundwater in the unconsolidated sediments on‐site
and down‐gradient of the Site is unknown. Additional off‐site, down‐gradient, groundwater
monitoring wells should be installed, monitored, and sampled within the unconsolidated
groundwater.
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The lateral and vertical extent of COCs in the bedrock aquifer is unknown, especially to the
southwest of the Site along the strike of the siltstone bedrock and to the northwest along
the dip of the siltstone bedrock. Additional discretely screened on‐ and off‐site bedrock
monitoring wells should be installed, monitored, and sampled.
Given the currently observed magnitude and extent of off‐site groundwater contamination,
and the likely full extent once delineation is complete, off‐site remediation is required to: 1)
Limit impact to WSWs; 2) Limit risks from indoor vapor intrusion; and 3) Restore the
groundwater resource to its pre‐impacted condition.
MTBE has been detected at concentrations as high as 28.7 µg/L at the Livingston Township
PSW #11, located approximately 1,750 feet northwest of the Site. Given the detection of
MTBE at this public well, a well‐head treatment system should be designed and permitted.
The system need not be installed at this time, but should be ready for immediate installation
should MTBE and/or other COCs be consistently detected at PSW #11.
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10.0 KEY OPINIONS
The following summarizes the key findings of the investigative and remedial activities conducted
to date, and our opinions based on the data reviewed:
1. Releases of gasoline containing MTBE have occurred at the Site. Gasoline releases have
been reported at the Site in May 2001, November 2001, May 2004, and April 2006. The
magnitude and distribution of groundwater contamination in 2002 indicates that a larger
release of gasoline containing MTBE occurred prior to 2002. See Section 8.2.
2. MTBE has impacted soil and groundwater beneath the Site. MTBE contamination was first
detected in groundwater beneath the Site in January 2002. See Section 6.2.
3. TBA has impacted soil and groundwater beneath the Site. TBA contamination was first
detected in groundwater beneath the Site in January 2002. See Section 6.2.
4. MTBE has migrated off‐site beyond the Site boundaries. MTBE contamination in
groundwater was first detected in October 2005 in off‐site well MW‐10D. See Section 6.4.
5. TBA has migrated off‐site beyond the Site boundaries. TBA contamination in groundwater
was first detected in October 2005 in off‐site well MW‐10D. See Section 6.4.
6. Groundwater contamination has not co‐mingled with releases from nearby facilities. There
is no indication that contamination from the Site has co‐mingled with releases of gasoline at
other facilities.
7. Investigations have failed to delineate the extent of MTBE contamination in groundwater
laterally. MTBE contamination is not delineated in groundwater to the southwest of the Site
in the unconsolidated sediments. MTBE contamination is not delineated in bedrock
groundwater to the southwest and northwest of the Site. See Section 6.4.3.
8. Investigations have failed to delineate MTBE in groundwater vertically. MTBE contamination
has been detected in Zone D bedrock groundwater monitoring wells. No deeper bedrock
zones have been installed and sampled. See Section 6.4.3.
9. Investigations have failed to delineate the extent of TBA contamination in groundwater
laterally. TBA contamination is not delineated in groundwater to the southwest of the Site in
the unconsolidated sediments. TBA contamination is not delineated in bedrock
groundwater to the southwest and northwest of the Site. See Section 6.4.3.
10. Investigations have failed to delineate TBA in groundwater vertically. TBA contamination has
been detected in Zone D bedrock groundwater monitoring wells. No deeper bedrock zones
have been installed and sampled. See Section 6.4.3.
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January 2013
aquilogic
11. MTBE contamination in groundwater exists beyond the current monitoring network. MTBE
contamination has been detected in the most down‐gradient groundwater monitoring wells.
See Section 6.4.3.
12. TBA contamination in groundwater exists beyond the current monitoring network. TBA
contamination has been detected in the most down‐gradient groundwater monitoring wells.
See Section 6.4.3.
13. Remediation performed to date has failed to fully address on‐site groundwater
contamination. Asymptotic concentrations have not been achieved by the on‐site P&T
system. Additional investigation is required to further evaluate the effectiveness of the on‐
site remediation system.
14. Remediation performed to date has failed to effectively control the off‐site migration of
groundwater contamination. Contamination has migrated off‐site in unconsolidated
sediments to the southeast and in bedrock to the southwest and northwest. See Section
6.4.3.
15. Remediation performed to date has failed to effectively remediate off‐site groundwater
contamination. To date, no off‐site remedial actions have been implemented. See Section
6.4.3.
16. Additional off‐site investigation is required. Groundwater contamination is not delineated to
the southwest and northeast of the Site. See Section 6.4.3.
17. Investigation of deeper groundwater zones is required. Contamination has been detected in
Zone D bedrock groundwater monitoring wells. No deeper bedrock zones have been
installed and sampled. See Section 6.4.3.
18. Additional on‐site remediation of groundwater is required. The on‐site remediation systems
have not reached asymptotic levels.
19. Additional off‐site remediation of groundwater is required. To date, no off‐site
groundwater remediation has been conducted at the site. The magnitude and extent of
contamination in groundwater warrants remediation. See Section 6.4.3.
20. Releases pose a threat to deeper aquifers. Contaminants have been detected to a depth of
121 feet bgs on‐site within the deepest bedrock unit investigated. MTBE has been detected
in a commercial supply well at 19 South Livingston Avenue (screened to a depth of 298 feet).
MTBE has been detected at PSW #11 (screened from 54 to 423 feet bgs). See Section 6.4.3,
8.3, 8.4.
21. Releases pose a threat to, and have impacted, WSWs. MTBE contamination has been
detected in a commercial supply well 700 feet to the southwest and a PSW located 1,750
feet to the northwest. Additional vapor intrusion studies are needed to evaluate the risks to
nearby building occupants. See Section 8.5.
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Revised Site Summary Report
ID # ‐ 8857 Exxon Service Station #31310
January 2013
aquilogic
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