PUBLIC HEALTH ASSESSMENT
NEW HAMPSHIRE PLATING COMPANY
MERRIMACK, HILLSBOROUGH COUNTY, NEW HAMPSHIRE ENVIRONMENTAL CONTAMINATION AND OTHER HAZARDS
The tables in this section list the contaminants of concern. The contaminants are evaluated in subsequent sections of this public health assessment, and it is determined whether exposure to them has public health significance. ATSDR selects and discusses contaminants using the following factors:
In the data tables in the On-site and Off-site Contamination subsections, the fact that a contaminant is listed does not mean that it will cause illness or injury if exposures occur. Instead, the list specifies contaminants that will be further evaluated in the public health assessment.
The data tables include the following abbreviations:
CREG = Cancer Risk Evaluation Guide
EMEG = ATSDR Environmental Media Evaluation Guide
MCLG = EPA Maximum Contaminant Level Goal
MCL = EPA Maximum Contaminant Level
ppm = parts per million
ppb = parts per billion
RfD = EPA Reference Dose
RfC = EPA Reference Concentration
RMEG = Reference Dose Media Evaluation Guide
AHA = American Heart Association
ATSDR health assessment comparison values are contaminant concentrations in specific media used to select contaminants for further evaluation. Those values include environmental media evaluation guides (EMEGs), cancer risk evaluation guides (CREGs), reference dose media evaluation guides (RMEGs) and other relevant guidelines.
EMEGs are media-specific comparison values that are used to select contaminants of concern at hazardous waste sites. EMEGs are derived from the Minimal Risk Levels (MRLs) presented in the ATSDR Toxicological Profiles. An MRL is an estimate of daily human exposure to a chemical that is likely to be without a substantial risk of harmful (noncancerous) effects over a specified duration of exposure. EPA's reference dose (RfD) and reference concentration (RfC) are estimates of the daily exposure to a contaminant unlikely to cause illness or injury. RMEGs are media-specific comparison values that are used when EMEGs are not available. RMEGs are derived from RfDs.
CREGs are estimated contaminant concentrations based on the incidence of one excess cancer in a million persons exposed over a lifetime. CREGs are calculated from EPA's cancer slope factors. EPA's maximum contaminant level goal (MCLG) is a drinking water health goal. Maximum contaminant levels (MCLs) are contaminant concentrations in water that EPA deems protective of public health (considering the availability and economics of water treatment technology) over a lifetime (70 years) at an ingestion exposure rate of 2 liters of water per day. MCLs are regulatory concentrations; MCLGs are not.
Between 1981 and 1991, various samples from on-site environmental media were analyzed. The collection and analyses of the samples were initiated by NHPC, NHDES, or EPA.
For purposes of this public health assessment, on site is considered within the site perimeter fence.
Waste Material-Lagoon Surface Water and Effluent (wastewater)
Between September 1981 and July 1986, 41 samples of lagoon water and 28 samples of effluent
were analyzed. Between September 1983 and October 1984, samples of effluent from the NHPC
operation, which discharged into the NHPC lagoon, and surface waters of the Lagoon #1 were
collected monthly and analyzed for cyanide. Most of the other samples collected from those
media were analyzed for volatile organic compounds (VOC) and for selected inorganic
compounds (1). The maximum contaminant concentrations for the on-site lagoon surface water
and effluent are shown in Table 1. The data reflect contaminant levels before lagoon remediation
(i.e., removal) began.
Table 1. Maximum Contaminant Concentration in On-site Waste
Materials-Lagoon
Surface Water and Effluent Water
Contaminant | Maximum Concentration (ppm) |
Ref | Comparison Valuea | |
(ppm) | Source | |||
Cadmium | 17.0 | 1 | .007 | EMEG |
Chromium (VI) | 5.3b | 1 | .050 | EMEG |
Chromium-total | 15.0 | 7 | 10.0 | EMEG |
Copper | 7.0 | 7 | 1.30 | MCL |
Nickel | 90.0 | 7 | .100 | MCL |
Zinc | 95.0 | 7 | 3.0 | RMEG |
Total Cyanide | 140.0 | 7 | .200 | RMEG |
Tin | 24.2 | 1 | NA | NA |
Carbon tetrachloride |
95 | 7 | .0003 | CREG |
1,2-Dichloroethane | 261 | 7 | .0004 | CREG |
1,1,1-Trichlorethane | 238 | 7 | .200 | MCL |
Trichloroethene | 52 | 7 | .003 | CREG |
a- EMEG and RMEG comparison values reported for children.
b- Value for chromium +6 obtained from one sample of effluent--corresponding total chromium
value was reported at 9.8 ppb.
NA- Not Available.
Waste Material-Lagoon Sludge
Between 1981 and early 1989, about 24 samples of lagoon sludge were obtained and analyzed primarily for selected heavy metals and cyanide. The most comprehensive sampling of the extent of contamination in the lagoon area was performed by EPA in October 1989. One objective of that sampling was to determine the vertical and lateral extent of contamination in the four on-site lagoons. A total of 163 sludge samples, at depths ranging from 0-12 feet, were obtained in a grid fashion from the four lagoons (12). The 0-foot samples were obtained within the first three inches of sludge (13). Of the 163 samples, 117 were analyzed for selected heavy metals (i.e., cadmium, chromium, lead, nickel, and zinc); 34 samples were analyzed for selected heavy metals and cyanide; and 12 samples were analyzed for cyanide only (12). On January 21, 1991, EPA collected five grab samples of lagoon sludge to determine concentrations of chromium (VI) in relation to total chromium concentrations. The results of that limited sampling indicate that most of the chromium in the lagoon sludge at the time of sampling was in the less toxic form (i.e., Cr (III)). The maximum contaminant concentrations in on-site lagoon sludge are shown in Table 2. Those data reflect contaminant levels before lagoon remediation (i.e., removal) began.
Soil
In May 1987, five soil samples were obtained from beneath the NHPC facility building. The
composite samples were obtained at a maximum depth of 18 inches (2). In addition, during the
comprehensive sampling of the lagoon sludge, which was performed by EPA in October 1989,
some 34 samples were collected to determine the extent of contamination in the soil adjacent to
the lagoons, and as part of an ecological study (11,12). Samples were collected at depths ranging
from 0-12 feet. Surface soil samples were collected at a depth of 0-3 inches (13). The 1987 soil
samples were analyzed for selected heavy metals and cyanide. Of the 34 samples collected in
October 1989, 27 were analyzed for selected heavy metals, four for the same heavy metals and
cyanide, and three for cyanide only (12).
Table 2. Maximum Contaminant Concentrations of Waste Material-Lagoon Sludge
Contaminant | Maximum Concentration (ppm) |
Ref. | Comparison Valuea | |
(ppm) | Source | |||
Cadmium | 89,200b/16,000c | 1,12 | 40 | EMEG |
Chromium-total | 28,000c | 12 | 300d/50,000e | RMEG |
Copper | 62,000b | 1 | 300f | RMEG |
Lead | 1,100b/430c | 12 | NA | NA |
Nickel | 16,000c | 12 | 1,000g | RMEG |
Tin | 26,000c | 12 | NA | NA |
Zinc | 160,000c | 12 | 20,000 | RMEG |
Total Cyanide | 23,700c | 12 | 1,000 | RMEG |
a- EMEG and RMEG comparison values reported for children.
b- Depth of sample containing maximum concentration not known.
c- Surface sludge sample obtained from a depth of 0 - 3 inches.
d- RMEG for chromium (VI).
e- RMEG for chromium (III).
f- RMEG for copper cyanide.
g- RMEG for nickel.
NA- Not Available.
During April and May 1990, EPA investigated the extent and degree of soil contamination by
VOCs and heavy metals at the site. The NHPC site (excluding lagoons) was partitioned into
three plots of land, on which a 50-foot-square grid system was established. Soil samples (156)
were collected by removing 2-4 inches of soil; the samples were screened on site for heavy
metals. Soil samples (173) were collected at a depth of 2-2.5 feet and screened on site for VOCs.
Thirty-two duplicate soil samples were collected and sent to the EPA laboratory for VOC
analysis; 17 duplicate soil samples were sent to the EPA laboratory for heavy metal analysis.
Three of the soil samples were also analyzed for cyanide (14). The maximum on-site surface soil
contaminant concentrations are summarized in Table 3. Those values are for contaminant
concentrations in soil that have not been remediated and remain on site.
Table 3. Maximum Contaminant Concentrations in On-site Surface Soil Samples
(0-3 inches)
Contaminant | Maximum Concentration (ppm) |
Ref. | Comparison Valuea | |
(ppm) | Source | |||
Cadmium | 370 | 11 | 40 | EMEG |
Chromium-total | 470/800b | 11 | 300c/50,000d | RMEG |
Lead | 448 | 14 | NA | NA |
Tin | 102/3,000b | 14 | NA | NA |
Zinc | 2,100/2,500b | 11 | 20,000 | RMEG |
a- EMEG and RMEG comparison values reported for children.
b- Value represents an on-site screening concentration only-- sample was not sent to laboratory
for confirmation.
c- RMEG for chromium +6.
d- RMEG for chromium +3.
Building Interior Contamination
On February 2, 1990, EPA collected four interior building samples from the NHPC facility. Three samples were taken from the laboratory, main shop, and the line and zinc room by sweeping dusts and other small particles; one sample was taken from the office vacuum cleaner. The samples were analyzed by X-ray fluorescence for selected heavy metals (total chromium, lead, nickel, zinc, cadmium, and tin) (15). In addition, on May 4, 1990, EPA entered the NHPC building. Ambient air throughout the building was screened for VOCs and combustible gases--no VOCs were detected above background, and oxygen levels were in the normal range.
Soil samples were taken from a trench in the NHPC building. Four soil samples were collected and screened for VOCs; three soil samples were collected and screened for heavy metals; and one duplicate sample was collected and sent to the EPA laboratory for VOC and heavy metal analysis. In addition, four bulk asbestos samples were taken--two from an air-cell-type pipe insulation and two from ceiling tiles. Asbestos was found at a maximum 30 % in one pipe insulation sample--the type of asbestos found was chrysotile. Asbestos was not found in two ceiling tile samples (14). The maximum contaminant concentrations in the NHPC building were detected in samples of dust and other small particles--those data are summarized in Table 4.
Table 4. Maximum Contaminant Concentrations in NHPC Building
Interior
Contaminant | Maximum Concentration (ppm) |
Ref. | Comparison Valuea | |
(ppm) | Source | |||
Cadmium | 3,430 | 7 | 500 | EMEG |
Chromium-total | 16,520 | 7 | 4,000b/700,000c | RMEG |
Zinc | 60,650 | 7 | 200,000 | RMEG |
Nickel | 3,220 | 7 | 10,000 | RMEG |
Tin | 8,210 | 7 | NA | NA |
a- EMEG and RMEG comparison values reported for an adult.
b- RMEG for chromium +6.
c- RMEG for chromium +3.
NA- Not Available.
On-Site Groundwater - Monitoring Wells
Between 1981 and 1990, groundwater quality has been investigated on numerous occasions. During that period, about 20 on-site overburden (shallow) aquifer monitoring wells were installed and sampled. In addition, two on-site bedrock monitoring wells were installed and sampled. Sampling of those wells was initiated by NHPC, NHDES, and EPA. In June 1990, 13 on-site monitoring wells were analyzed for total cyanide, dissolved metals (filtered samples), and VOCs; some were also analyzed for base neutral and acid extractable compounds (i.e., semi-volatile organic compounds)(16). Most of the samples collected before June 1990 were analyzed for VOCs, heavy metals, and total cyanide--those samples were not filtered before analysis. Groundwater samples from on-site bedrock monitoring wells were not analyzed for heavy metals. Samples collected in December, 1993 as part of the RI/FS were analyzed for VOCs, total metals and cyanide. Five metals and eight VOCs were detected at levels above their respective MCLs.
The maximum contaminant concentrations detected in on-site groundwater samples were from
the overburden aquifer (Table 5). Some of the maximum inorganic contaminant concentrations
reported in Table 5 were detected in unfiltered samples. Several contaminants of concern were
also detected in samples of water from the bedrock aquifer. Trichloroethene (115 ppb) was the
only VOC detected at levels above comparison values in samples of on-site bedrock aquifer
groundwater (Table 5). Cyanide and 1,1,1-trichloroethane were detected, but were not above
comparison values.
Table 5. Maximum Contaminant Concentrations in On-site
Groundwater Monitoring Wells
Contaminant | Maximum Concentration (ppb) |
Ref | Comparison Valuea | |
(ppb) | Source | |||
Arsenic | 230 | 42 | 0.2 | CREG |
Cadmium | 529 | 42 | 7 | EMEG |
Chromium-total | 536 | 1 | 50b/10,000c | RMEG |
Lead | 200 | 1 | 0/15d | MCLG/MCL |
Manganese | 2,130 | 1 | 50 | RMEG |
Mercury | 5 | 1 | 2 | LTHA |
Selenium | 46 | 1 | 30 | EMEG |
Tin | 12,000 | 7 | NA | NA |
Zinc | 530 | 7 | 2,000 | LTHA |
Total Cyanide | 1,550 | 7 | 200e | RMEG |
Sodium | 220,000 | 1 | 20,000 | AHA |
Benzene | 32.9 | 1 | 1.0 | CREG |
Cyclohexane | 77.4 | 1 | NA | NA |
Chloroform | 234 | 1 | 6.0 | CREG |
Xylenes-o and p | 1,500 | 1 | 10,000 | LTHA |
1,1-Dichloroethane | 1,840 | 7 | 81 | DPHS |
1,1-Dichlorethene | 920 | 7 | .06 | CREG |
1,2-Dichlorethene | 121 | 7 | 70 | MCL |
Isobutyl ketone | 357 | 7 | NA | NA |
Tetrachloroethene | 37.9 | 1 | 0/5 | MCLG/MCL |
Trichloroethene | 7500 | 42 | 3 | CREG |
1,1,1-Trichlorethane | 3,264 | 1 | 200 | LTHA |
a- EMEG and RMEG values reported for children.
b- RMEG for chromium (VI)
c- RMEG for chromium (III)
d- EPA Action Level
e- RMEG for free cyanide
NA- Not Available
On-Site Ambient Air
During the excavation and treatment of soils and sludge material performed by EPA from June to
November 1990, ambient air samples were collected. A system of 11 on-site and five off-site
(perimeter) monitoring stations was designed. On any given day, only part of the monitoring
system would operate, depending on the location of on-site activities and wind direction.
Real-time measurements were also obtained on-site to measure organic vapors and hydrogen
cyanide generation. No detectable concentrations of organic vapors or hydrogen cyanide were
measured. One of the off-site monitoring stations is located directly behind the nearby child
daycare center. The monitoring devices at those stations sampled for cadmium, chromium, and
cyanide dusts. Conditions during collection of most samples were hot (greater than 80 oF)and
dry(18). Such conditions probably are a worst-case scenario for generation of VOCs and dusts
(particulates). A summary of the contaminant concentration ranges for on-site ambient air is
shown in Table 6.
Table 6. Range of Contaminant Concentrations in On-site Air Samples
Contaminant | Concentration Range (mg/m3) |
Ref. | Comparison Value | |
(mg/m3) | Source | |||
Total Cyanide | ND-0.032 | 9 | NA | NA |
Total Chromium | ND-0.003 | 9 | 8.0X10-8 | CREGa |
Cadmium | ND | 9 | 6.0X10-7 | CREG |
a- CREG reported for chromium (VI). B. Off-site Contamination
ND- Not Detected.
NA- Not Available.
Off-Site Surface Water
Between 1982 and 1990, NHDES collected 24 surface water samples from Horseshoe Pond, which were analyzed for VOCs, selected heavy metals, and cyanide (1,18). The 1982 samples from Horseshoe Pond contained the three highest concentrations of cyanide found in any sample of water from Horseshoe Pond (i.e., 50, 160, and 580 ppb). One 1982 pond sample contained cadmium at 2 ppb. A more recent analyses of water from Horseshoe Pond carried out under the RI/FS in July of 1993 yielded non-detect results for cyanide, VOCs and metals including cadmium (18).
Between 1986 and 1988, NHDES collected five water samples from the Merrimack River
upstream from, adjacent to, and downstream of the site. Those samples also were analyzed for
VOCs, selected heavy metals and cyanide. One sample from the Merrimack River taken prior to
the RI/FS showed cyanide at a concentration of 12 ppb (1). Sampling of Merrimack river surface
water during the RI/FS detected no cyanide, VOCs or metals. Contaminant concentrations in
off-site surface water are summarized in Table 7.
Table 7. Range of Contaminant Concentrations in Off-Site Surface Water
Contaminant | Concentration Range (ppba) |
Ref | Comparison Valueb | |
(ppb) | Source | |||
Cadmium | ND-2 | 1,18 | 7 | EMEG |
Chromium-total | ND | 1,18 | 50c/10,000d | RMEG |
Total cyanide | ND-580 | 1,18 | 200d | RMEG |
Volatile organic compounds | ND | 1,18 | NR | NR |
a-Maximum concentrations reported were detected in 1982
samples from Horseshoe Pond
b- EMEG and RMEG values reported for children
c- RMEG for chromium +6
d- RMEG for chromium +3
e- RMEG for free cyanide
NR- Not Relevant
ND- Not Detected
Off-Site Sediment
During February 1991, EPA collected ten grab samples of sediment from the Merrimack River.
The samples were taken upstream from, adjacent to, and downstream of the site. The samples
were analyzed for cadmium, total chromium, chromium +6, and total cyanide (19). Sediment
sampling of Horseshoe Pond was conducted in July of 1993 as part of the RI/FS. Sediment
samples were taken in a radial pattern around the pond and analyzed for metals, cyanide, VOCs
and semi-volatile organic chemicals (SVOCs)(42). Contaminant concentrations in off-site
sediment from the Merrimack River and Horseshoe Pond are summarized in Table 8.
Table 8.Range of Contaminant Concentrations in Off-Site Sediment
Contaminant | Concentration Range (ppm) |
Comparison Valuea | |
(ppm) | Source | ||
Arsenic | 1.5-15.0 | 0.4 | CREG |
Benzo(a)anthracened | 0.93 | NA | NA |
Benzo(a)pyrened | 0.069 | 0.1 | CREG |
Benzo(b)flouranthened | 0.140 | NA | NA |
Bis(2-ethylhexyl)Phthalated | 0.240 | NA | NA |
Cadmium | ND-0.76 | 40 | EMEG |
Chromium (VI) | ND | NA | NA |
Chromium-total | 5.9-53.3 | 50,000b | RMEG |
Chrysened | 0.089 | NA | NA |
Copper | ND-37.6 | 300c | RMEG |
Lead | 4.0-107.0 | NA | NA |
Nickel | ND-24.1 | 1,000 | RMEG |
Phenanthrened | 0.067 | NA | NA |
Pyrened | 0.180 | 2,000 | RMEG |
Total cyanide | ND | NA | NA |
1,1,1-Trichloroethane | 0.006 | NA | NA |
Zinc | 14.6-167.0 | 20,000 | RMEG |
a- EMEG and RMEG comparison values reported for children.
b- EMEG for chromium +3
c- RMEG for copper cyanide
d- PAH detected in single Horseshoe Pond sediment sample(HP-07)
ND- Not Detected
NA- Not Available
Off-Site Soil
During on-site sampling by EPA in 1990, three samples of off-site soil were collected adjacent to Wright Avenue across the street from NHPC (i.e., the YMCA property). Those off-site samples were obtained and screened in the same manner as on-site soil samples. One duplicate sample was sent to the EPA laboratory for heavy metal analysis and confirmation. Heavy metals were not detected above background levels in any of the three off-site samples.
Off-Site Ambient Air
See the discussion concerning on-site ambient air for details of off-site air sampling performed at
the site. During the June through August 1990 excavation period, cyanide was detected eight
times at off-site monitoring stations. Cyanide was detected three times at the day care center
monitoring station; the maximum cyanide value detected was 0.026 mg/m3--this was the
maximum value detected off-site. Cadmium was detected in only one on- or off-site sample--the
day care center (17). Contaminant concentration ranges for off-site ambient air are summarized in
Table 9.
Table 9.Range of Contaminant Concentrations in Off-site Air Samples
Contaminant | Concentration Range (mg/m3) |
Ref. | Comparison Value | |
(mg/m3) | Source | |||
Total cyanide | BD-0.026 | 17 | NA | NA |
Total Chromium | BD | 17 | 8.3X10-8 | CREGa |
Cadmium | BD-0.0003 | 17 | 5.6X10-7 | CREG |
Off-Site Groundwater - Monitoring Wells
Between 1981 and 1990, groundwater quality near the site had been investigated on numerous occasions. During that period, 36 off-site surficial aquifer monitoring wells were installed and sampled. In addition, three off-site bedrock monitoring wells were installed and sampled. One bedrock production well, used by Jones Chemical Inc. as a source of industrial cooling water, was also sampled. Off-site sampling of the monitoring wells was initiated by NHPC, NHDES, EPA, and several commercial entities that abut the NHPC property. In June of 1990, 32 samples from off-site monitoring wells were analyzed for total cyanide, dissolved metals (filtered samples), and VOCs. Some were also analyzed for base neutral and acid extractable compounds (i.e., semi-volatile organic compounds) (16). Most of the samples collected before June 1990 were analyzed for VOCs, heavy metals, and total cyanide. Further sampling was carried out in December, 1993 as part of the RI/FS. The maximum contaminant concentrations detected in off-site groundwater were from samples taken from the overburden aquifer--those concentrations are shown in Table 10.
Several VOCs were detected above their comparison values in groundwater samples from off-site bedrock monitoring wells (Table 10). The VOCs detected included chloroform (8 ppb), 1,2-dichloroethene (2 ppb), and trichloroethene (115 ppb) (1). The 1,2-dichloroethene and the trichloroethene were detected in water samples from the Jones Chemical Production well. Several heavy metals and cyanide were detected at concentrations below their respective comparison values in groundwater samples drawn from the bedrock aquifer.
Off-Site Public and Private Water Supply Wells
In March 1990, samples from a private drinking water well and the Jones Chemical production well, both on Daniel Webster Highway, were analyzed for VOCs. The private well was resampled in August of 1993 (43). Two nearby MVWD municipal water supply wells are monitored monthly for lead and copper and annually for VOCs, radon, and other priority compounds (20). No contaminants were detected in samples from these two off-site municipal wells.
Maximum contaminant concentrations detected in the two samples taken from the off-site private
well are summarized in Table 11. VOC contamination was also detected in the Jones Chemical
supply well but is not included in the table below since this well is not used for domestic
purposes. No contaminants detected in the Jones Chemical production well exceeded their
respective MCLs.
Table 10. Maximum Contaminant Concentrations in Off-site
Groundwater Monitoring Wells
Contaminant | Maximum Concentration (ppb) |
Ref. | Comparison Valuea | |
(ppb) | Source | |||
Arsenic | 190 | 1 | 0.2 | CREG |
Cadmium | 112 | 16 | 7 | EMEG |
Chromium-total | 180 | 1 | 50b/10,000c | RMEG |
Lead | 20 | 1 | 0/50 | MCLG/MCL |
Manganese | 1,290 | 1 | 50 | RMEG |
Mercury | 2.2 | 1 | 2 | LTHA |
Total Cyanide | 390 | 1 | 200 | RMEG |
Sodium | 4,300,000 | 1 | 20,000 | AHA |
Bromochloromethane | 45 | 1 | 90 | LTHA |
Carbon tetrachloride | 61 | 1 | 0.3 | CREG |
Chloroform | 3,200 | 1 | 6.0 | CREG |
1,1-Dichloroethane | 50 | 1 | 81 | DPHS |
1,1-Dichlorethene | 63 | 42 | .06 | CREG |
Tetrachloroethene | 180 | 1 | 0/5 | MCLG/MCL |
Trichloroethene | 2,000 | 7 | 3 | CREG |
1,1,1-Trichlorethane | 3,225 | 1 | 200 | LTHA |
Table 11. Maximum Contaminant Concentrations in Off-site
Private Water Supplies
Contaminant | Maximum
Concentrationa (ppb) |
EPA Cancer Class |
Ref. | Comparison Value | |
(ppb) | Source | ||||
1,1-Dichloroethane | 0.93 | C | 43 | 81 | DPHS |
1,1-Dichloroethene | 1.5 | C | 7 | .06/7 | CREG/MCL |
1,1,2,2-Tetrachloroethane | 2.6 | C | 7 | 0.2 | CREG |
1,1,1-Trichloroethane | 4.3 | NA | 42 | 200 | MCL |
Tetrachloroethene | 3.6 | B2-C | 42 | 0.7/5 | CREG/MCL |
Trichloroethene | 1.2 | B2-C | 43 | 3/5 | CREG/MCL |
Trichloromethane (chloroform) |
1.2 | B2 | 43 | 6.0/100 | CREG/MCL |
a- Maximum concentrations reported for two samples from the off-site private drinking water
well on Daniel Webster Highway.
C. Toxic Release Inventory Data
To identify facilities that could contribute to the air, surface water, and soil contamination near
the NHPC site, ATSDR searched the 1987, 1988, and 1989 Toxic Release Inventory (TRI). TRI
is a database developed by EPA from chemical release (air, water, and soil) information provided
by certain industries. In this case, TRI contained information about air releases in the Merrimack
area and in the zip code in which the site is located. However, because these releases were from
facilities at least one mile from the site, and the most significant release was from a facility at
least two miles from the site, it is not likely that those contaminants affected air quality in the
vicinity of the NHPC site (21).
D. Quality Assurance and Quality Control
Data on quality assurance/quality control (QA/QC) techniques used during preparation of this
public health assessment were not available for review. It is believed, however, that most of the
data in this assessment were produced by qualified laboratories contracted by NHDES or EPA.
Furthermore, all of the samples collected or analyzed by the NHDES or EPA contractors have
passed strict QA/QC requirements.
E. Physical and Other Hazards
No physical hazards were apparent at the site. Any remaining equipment or other hazards in the
NHPC building are well secured.
PATHWAYS ANALYSES
To determine whether nearby residents are exposed to on-site contaminants or to those migrating from a site, ATSDR evaluates the environmental and human components that lead to human exposure. This pathways analysis consists of five elements: source of contamination; transport through an environmental medium; a point of exposure; a route of exposure, and an exposure population. The first three elements pertain to environmental pathways,--the two remaining elements pertain to human exposure pathways.
ATSDR categorizes exposure pathways as either completed or potential. For a completed
pathway to exist, five elements must be present and there must be evidence that exposure to a
contaminant has occurred, is occurring, or will occur. A pathway is potential when at least one
of the five elements is missing, but could exist. Potential pathways indicate that exposure to a
contaminant could have occurred, could be occurring, or could occur in the future. An exposure
pathway is eliminated if at least one of the five elements is missing and will never be present.
Table 12 identifies the completed exposure pathways at NHPC; Table 13 identifies the site's
potential exposure pathways. The discussion following the two tables address only pathways
important and relevant to the site. Also discussed are some of the eliminated pathways and those
about which there is community concern.
TABLE 12. COMPLETED EXPOSURE PATHWAYS
PATHWAY NAME | EXPOSURE PATHWAY ELEMENTS | TIME | ||||
SOURCE | ENVIRONMENTAL MEDIA | POINT OF EXPOSURE | ROUTE OF EXPOSURE | EXPOSED POPULATION | ||
NHPC Waste Material |
NHPC Effluent/ NHPC On-site activities |
Sludge Soils Surface water |
On-site Lagoons and Soils |
Ingestion Skin contact |
Children playing on site (20) |
Past |
Ambient Air | NHPC Lagoons |
Air | Day Care Center | Inhalation | Children (20) | Past |
NHPC Building |
Interior NHPC Building |
Dusts and Other small particles | Work Surfaces Interior NHPC Building | Ingestion | NHPC workers (30) |
Past |
Private Well (Daniel Web. Hwy) |
Site-unrelated | Groundwater | Residential (tap) |
Ingestion Inhalation Skin contact |
Residents using
private well (12) |
Past Present Future |
( ) - Estimated exposed population.
TABLE 13. POTENTIAL EXPOSURE PATHWAYS
PATHWAY NAME | EXPOSURE PATHWAY ELEMENTS | TIME | ||||
SOURCE | ENVIRONMENTAL MEDIA | POINT OF EXPOSURE | ROUTE OF EXPOSURE | EXPOSED POPULATION | ||
NHPC Waste Material |
Lagoon Waste Material Soils |
Air | On-site Lagoons | Inhalation | Children Playing On-site | Past |
Private Wells | NHPC | Groundwater | Private Wells (Litchfield) |
Ingestion Inhalation Skin contact |
Users of Private wells in Litchfield |
Past Present Future |
Merrimack River | NHPC | Fish Sediment Surface Water |
Merrimack River | Ingestion Skin contact |
Recreational use of Merrimack River | Past Present Future |
NHPC Workers | Work Surfaces/ Interior NHPC Building | Air | Interior NHPC Building | Inhalation | NHPC workers | Past |
Horseshoe Pond (Surface water and Sediment) |
NHPC | Sediment Surface water | Horseshoe Pond | Ingestion Skin contact |
Recreational users of Horseshoe Pond | Past Present Future |
Horseshoe Pond (Fish) | Site-unrelated mercury | Groundwater Sediment Surface Water |
Fish | Ingestion | Consumers of fish from Horseshoe Pond | Past Present Future |
A. Completed Exposure Pathways
NHPC Waste Material Pathway
Since children played on-site before site restrictions were in place, they were probably exposed to on-site waste material. Waste materials included lagoon sludge, soils, and surface water. The greatest exposure to contaminants was from the waste materials in the lagoon system, although soils at other on-site locations also were probable points of exposure. It is likely that exposure to lagoon sludge contaminants varied depending on the dryness of the sludges (Table 12).
The lagoon system, soils near the lagoon, and the undefined wetlands are contaminated primarily because of the discharge of effluent to the lagoon system. When the lagoon system overflowed, that discharge contaminated the near lagoon soils and the undefined wetlands. Contamination of other on-site soils probably resulted from other disposal methods or from leaks from pipes or storage tanks. The results of the extensive characterization of on-site soils near the perimeter of the site and the lack of a mechanism for transport of contaminants to off-site soils indicate that most, if not all, of the soil contamination is confined to on-site areas.
Soil ingestion is an important route of exposure for children who played on-site, particularly for children younger than 6 years (22). Soil ingestion typically is greater for young children because of their greater hand/mouth activity. Because the ages of the children who played on site are not known, however, it is difficult to determine the amount of soil they might have incidentally ingested. Furthermore, given the climatic conditions of New Hampshire, it is likely that cold weather and snow precluded recreational activities and contact with contaminated media at the site during part of the years that children probably were exposed. Children could have been exposed to contaminants at the site from the early 1960s until 1987-1989, when the lagoon fence was erected and remedial actions began. The number of children who played on site and how often they played there are not known. Given current conditions at the site, it is highly improbable that children now have appreciable exposure.
As shown in Tables 2 and 3, on-site surface sludge and soils have been contaminated with high levels of heavy metals and cyanide. In addition, high levels of VOCs and heavy metals were found in the NHPC effluent and in surface water in the lagoons (Table 1). EPA has remediated the most significant contaminant concentrations in the lagoon system (Table 2). The contaminant concentrations shown in Table 3 remain on site.
Ambient Air Pathway
Children who attended the Former Avanti Day Care Center that abuts the NHPC site possibly were exposed in the past to contaminated ambient air during site remediation activities that occurred during summer, 1990 (Table 12). According to ambient air monitoring data at an off-site sampling location behind the day care center, however, contaminants were detected only four times during this time period. Cyanide was detected three times at a maximum value of 0.026 mg/m3; cadmium was detected once at a concentration of 0.0003 mg/m3. Those concentrations probably reflect a worst-case scenario of off-site dust generation at the site because they were detected during remedial activity (i.e., when soils are disturbed) and during hot and dry conditions. When remediation was not taking place on site, the lagoons were usually wet because of discharge from the NHPC site and because they are natural water discharge areas. Localized dust generation during dry periods was reported when remedial workers walked on the dried lagoon sludge. There were no reports, however, of dust bowl-like conditions at the site.
NHPC Building Pathway
Former workers at the NHPC facility were probably exposed to high concentrations of heavy metals (Table 4) through ingestion of dusts and other small particles on work surfaces in the building (Table 12). The number of employees who worked at the site during its years of operation is not known. No future exposure pathways exist as the building was demolished in December of 1994.
Private Well Pathway
Contaminated water from one private well, located one-half mile southwest of the site represents possible past, current, and future exposure pathways (Table 12). That well is believed to be drawing water from the overburden aquifer. Since most, if not all, of the contaminated overburden groundwater is being discharged to the Merrimack River and Horseshoe Pond, it is not likely that contamination of the private well is related to the NHPC site. Therefore, it is likely that another unknown source of contamination exists and is contributing to the contamination of this well. No private wells used for domestic purposes or public water wells are believed to exist in the area of overburden groundwater contamination.
Since the contaminated private well is believed to supply a multiplex dwelling (presumably four
residential units), ATSDR estimates that approximately 12 persons were exposed to several
volatile organic chemicals (VOCs) by ingestion, inhalation, and skin contact. Since those
contaminants evaporate into the air from water during showers or baths, people are exposed as
they breathe the air in their homes. In addition, the contaminants are absorbed through the skin
during showers and/or baths, increasing exposure (23). Although the source of the private well
contamination is not known, and only two water samples from the well have been analyzed, it is
impossible to determine the duration and actual concentrations of exposure over time. Hence,
additional sampling and analyses of water from the private well are needed to completely
characterize this pathway.
B. Potential Exposure Pathways
NHPC Waste Material Pathway
Because children played on site before site restrictions were in place, it is possible that children breathed VOCs and soil dusts containing heavy metals and cyanide (Table 13). The source of the VOCs was the effluent and surface water in the lagoons; the soil dusts were from the lagoon sludge, near-lagoon soils, and other on-site areas with soil contamination. The primary points of exposure were the waste materials in the lagoon system and other on-site areas with soil contamination. Table 12 and the Completed Exposure Pathways section provide additional details on the exposure of children who once played on site.
No ambient air data for VOCs and soil dust are available to characterize the concentrations to which the children might have been exposed. Because this pathway relates, in part, to localized ambient air contamination in the past, sometimes caused by the use of all-terrain vehicles (ATVs) on site, those data will never be available. Given the high concentrations of heavy metals and VOCs in the on-site soils, sludge, effluent, and surface water (Tables 1-3), however, it is reasonable to assume that the ambient air pathway contributed to the total exposure of children who once played on site.
Private Well Pathway
The results of groundwater monitoring in the overburden and bedrock aquifers indicate that on- and off-site groundwater is contaminated with VOCs, heavy metals, and cyanide. Contaminated groundwater in the overburden aquifer has migrated from on-site source areas south, east, and southeast. The direction of contaminant migration is consistent with groundwater hydrology in the site area. The direction of contaminant migration in the fractured bedrock aquifer is not known. The bedrock aquifer monitoring network consists of two on-site and four off-site wells. Because the fractured bedrock is expected to influence groundwater flow in the bedrock aquifer, the localized movement of contaminants in groundwater cannot be characterized (1). Since the bedrock and overburden aquifers intercept to form one aquifer system, however, it is likely that some contaminated groundwater moves in the same direction as groundwater in the overburden aquifer (1). Hence, it is possible that contaminated bedrock groundwater has moved toward and under the Merrimack River; it is not known if the bedrock aquifer discharges to the river.
There are 43 private wells across the river in Litchfield, New Hampshire that are within a half-mile radius of the site. These wells represent potential points of exposure to contaminated groundwater, particularly if they are bedrock wells (Table 13). The current bedrock monitoring network does not, however, allow for characterizing that pathway. The Draft RI/FS has not adequately addressed this issue. It is unlikely that the two Litchfield public water wells, which are operated by the SNHWC, could become contaminated because they are about 3-4 miles from the site, and they do not draw water from the bedrock aquifer.
Groundwater contamination has been detected in monitoring wells on the YMCA property. A future potential exposure pathway exists for this property relative to the installation and use of drinking water wells.
Merrimack River Pathway
Surface Water and Sediment
The results of groundwater monitoring and hydrogeologic investigations indicate that groundwater contaminated with VOCs, cyanide, and possibly heavy metals, has migrated from on-site contaminant source areas to off-site areas east and southeast of the site. Some of those contaminants have probably discharged into the Merrimack River. To date, surface water and sediment monitoring data have not shown elevated levels of site-related contaminants, except cyanide in one surface water sample (12 ppb). Sampling of Merrimack River surface water conducted during the RI/FS yielded non-detect levels of VOCs, metals and cyanide. Sediment samples taken from the river during the RI/FS were non-detect for VOCs and within background ranges for metals.
Fish
Potential past, present, and future exposure to site contaminants that may bioaccumulate in fish is possible for individuals who have eaten or eat fish from the Merrimack River (Table 13). As indicated previously, however, the only contaminant detected at elevated levels in sediment and surface water samples from the Merrimack River was cyanide, at 12 ppb. Fish bioaccumulate very little cyanide into their bodies (24). Cyanide was detected in surface water only once at low levels; it was not detected at all in sediment samples. Therefore, it is not likely that fish are bioaccumulating cyanide at levels of public health concern.
NHPC Workers Pathway
Former NHPC workers might have been exposed in the past by way of inhalation of heavy metal-contaminated particles in indoor air (Table 13).
Data exist estimating ingestion exposure to dusts and other small particles in the NHPC building. However, no known data exist on dust in air inside the building to determine potential workers' exposure while NHPC was operating. Complete analysis of the indoor air pathway is not possible because current indoor air conditions do not represent conditions when the facility was operating (i.e., when workers were exposed). Specifically, remedial actions in the building have probably reduced ambient air dust levels; it is likely that the highest levels of contaminated dusts in ambient air were generated when workers disturbed contaminated work surfaces. Furthermore, given the high concentrations of heavy metals on work surfaces, ambient air exposure could have been significant.
Horseshoe Pond Pathway
Surface Water and Sediment
Results of groundwater monitoring and hydrogeologic investigations indicate that groundwater containing VOCs, cyanide, and possibly heavy metals has migrated from on-site contaminant source areas to off-site areas south of the site. Contaminated groundwater probably discharges at the northern shore of the outer bank of Horseshoe Pond. People swim near residential areas about 500 feet across the lake from the discharge point (Figure 1).
Surface water samples obtained in 1982 showed elevated levels of cyanide (up to 580 ppb). Cadmium was detected in one sample at 2 ppb. Analyses of the most recent surface water samples taken during the RI/FS in July, 1993 did not detect VOCs, metals or cyanide above detection limits. Sediment sampling of Horseshoe Pond was conducted in July, 1993 as part of the RI/FS. Samples were taken in a radial pattern around the pond. Several metals were detected at concentrations similar to background levels. Arsenic detected in one sample at a slightly higher level than background (15.6 ppm) is thought to result from naturally occurring sources. No on-site source of arsenic has been identified.
Based on Horseshoe Pond sediment and surface water sampling, past, current and future exposures to contaminants in these media are expected to be minimal.
Fish
As indicated previously, the only contaminants detected at elevated levels in surface water samples from Horseshoe Pond were cyanide and cadmium. Fish bioaccumulate very little cyanide (24). Since some fish species are bottom feeders, they are in close contact with sediment; therefore, the potential exists for fish to bioaccumulate site-related contaminants (e.g., cadmium) discharging into Horseshoe Pond.
This potential is estimated to be minimal based on recent sediment and surface water sampling. Sediment samples taken from Horseshoe Pond during the RI/FS were analyzed for several metals including arsenic, cadmium, chromium, copper, lead, nickel and zinc. Cadmium was not detected in any samples. Slight elevations in lead (HP-04) and arsenic (HP-06) concentrations were noted when compared to a representative background sample (HP-01). These increases are most likely due to background variability and do not represent a site related source. Lead and arsenic do not bioaccumulate in in the edible portion of fish and do not represent a hazard via this pathway.
It should be noted that NH DPHS has issued a health advisory for the ingestion of mercury in largemouth bass taken from Horseshoe Pond (see Appendix D-5). Mercury was not analyzed for in any sediment or surface water samples and is not thought to be a site related contaminant.
PUBLIC HEALTH IMPLICATIONS
A. Toxicological Evaluation
This section discusses health outcome data, health effects in individuals exposed to particular contaminants, and specific community health concerns. To evaluate health effects, ATSDR has developed minimal risk levels (MRLs) for contaminants commonly found at hazardous waste sites. The MRL is an estimate of a level of daily human exposure to a contaminant below which non cancerous adverse health effects are unlikely. MRLs are developed for each route of exposure (e.g., ingestion and inhalation) and for the length of exposure (e.g., acute, less than 14 days; intermediate, 15 - 364 days; and chronic, 365 days or more). Because ATSDR has no methodology to determine amounts of chemicals absorbed through the skin, the Agency does not have MRLs for skin exposure. ATSDR presents information on MRLs in its series of Toxicological Profiles on hazardous substances. These chemical-specific profiles provide information on health effects, environmental transport, human exposure, and regulatory status. The following discussion uses information obtained from the ATSDR Toxicological Profiles to identify health effects that might be related to site exposures.
Children Playing on the Site
ATSDR has determined that children playing on site were exposed to several contaminants (Table 14). Each contaminant is discussed by route of exposure. To estimate exposure dose, it was assumed that the children would ingest 200 milligrams (mg) of soil or sludge (dried), during an exposure period of 4 days. Exposures were estimated for 6-month periods. A surface water ingestion rate of 5 ml was used to estimate incidental ingestion of surface water by children playing in the lagoons.
Cadmium
Children were exposed to cadmium at the site through ingestion of NHPC surface water/effluent, NHPC waste material/lagoon sludge, and surface soil. Ingesting very high cadmium levels (0.07 mg/kg, estimated dose for children weighing 35 kg or approximately 77 pounds) severely irritates the stomach, leading to vomiting and diarrhea. Cadmium build up causes kidney damage in some people, and can lead to problems in calcium metabolism. As a result, bones become fragile and break easily. Skin contact with cadmium is not known to cause illness or injury in people or animals. The kidney is the main target organ of cadmium toxicity after extended oral exposure (27). Human studies have shown that prolonged cadmuim exposure can lead to a high incidence of abnormal kidney function, indicated by protein in the urine and a decrease in kidney function. Kidney abnormalities may increase in severity even after exposure has ended. Growing children are particularly sensitive to cadmium exposure.
As shown in Table 14 (at the end of this section), children were exposed to cadmium in dried sludge, and their estimated exposure dose exceeded the chronic MRL of 0.0002 mg/kg/day for cadmium ingestion. The estimated dose suggests that there is a possibility of mild kidney damage, indluding proteinuria, to occur. Proteinuria is the presence of increased protein in the urine. The estimated exposure dose for cadmium in the surface water and soil was below the chronic MRL for ingestion. However, that dose exceeds the emetic dose of 0.07 mg/kg/day and may lead to vomiting in some cases. No severe illness or injury would be expected. No evidence exists that people or animals exposed orally to cadmium have an increased incidence of cancer.
Chromium
Chromium, a naturally occurring element found in animals, plants, rocks, and soil and in volcanic dust and gases, was found in surface water, sludge, and soil on site. Chromium exists in three forms: chromium (II), chromium (III), and chromium (IV) Chromium (III) compounds are stable and are found in aerobic environments (e.g., top soil, surface water, ground water). Chromium (III) is an essential nutrient that helps the body use sugar, protein, and fat (28). Chromium (VI) is the second most stable form; it is found naturally in anaerobic environments, such as sediments. Chromium (IV) compounds are readily reduced to chromium (III) in the presence of oxidizable organic matter.
Inhaling or ingesting small amounts of chromium will not cause illness or injury. ATSDR does not have an intermediate or chronic MRL for chromium. EPA has set its reference dose (RfD) for chronic ingestion of chromium (VI) at 0.005 mg/kg/day and for chronic ingestion of chromium (III) at 1.00 mg/kg/day (28). An RfD is an estimate of the daily human exposure to a contaminant, over a lifetime, below which non-cancer health effects are unlikely to occur. Chromium ingestion by children playing on site should not cause illness or injury, except in individuals who are chromium sensitive. Those individuals may have dermatitis or skin irritation and inflammation. Chromium sensitivity, which is uncommon, usually develops after prolonged contact.
Copper
Copper, a reddish metal that occurs naturally in rock, soil, water, sediment, and air, as well as in plants and animals, is an essential element for all known living organisms including people and other animals. Food naturally contains copper. An individual typically will ingest about 1mg copper a day through normal eating and drinking. Children at NHPC were exposed to copper in surface water and sludge on the site. ATSDR does not have MRLs for copper, and EPA has no RfD for its ingestion. Children playing in surface water and sludge at NHPC should not experience severe health effects as a result of their copper exposure. Minor health effects that could occur following infrequent exposure to copper include diarrhea, abdominal pain, and vomiting (29).
Lead
Lead, a naturally occurring bluish-gray metal found in small amounts in the earth's crust, was found in sludge and soils at NHPC. Lead exposure is particularly dangerous for unborn children and young children because they are more sensitive to it during their development (25). The American Academy of Pediatrics considers lead a significant hazard to the health of children in the United States (30). The Centers for Disease Control (CDC) guidance on blood lead levels in children is 10 g/dl. ATSDR has no MRL, and EPA has no RfD for lead. Blood lead levels were not measured in children who played on the site. However, estimates of blood lead levels for children exposed to maximum lead levels in surface soil/sludge are not expected to reach 10 g/dl. Therefore, exposure to lead from on-site sources at NHPC are not expected to result in adverse health effects (44).
Nickel
Nickel, a hard, silvery white metal with no characteristic odor or taste, has properties that make it desirable for combining with other metals to form mixtures called alloys. Nickel is frequently alloyed with iron, copper, chromium and zinc (31). Rivers and lakes normally have low concentrations of nickel. Children at the site were exposed to nickel in surface water and sludge in lagoon areas at the site. Children could have been exposed to nickel in soil at the site by getting it on their skin or by eating it in dirt.
ATSDR does not have MRLs for nickel; they will be derived when sensitive endpoints (target organs) can be established. EPA does have an RfD for nickel (soluble salts) ingestion. The estimated doses of nickel to which children at the site were exposed do not exceed the RfD. Skin contact may cause red, irritated skin. Studies have shown that inhalation of nickel refinery dust and nickel subsulfide may cause cancer. No human or animal studies indicate that nickel ingestion can cause cancer. Children playing on the site are not expected to become ill or injured as a result of nickel exposure.
Tin
Tin , a soft, white, silvery metal found in small amounts in the earth's crust, is insoluble in water. Because simple tin compounds enter and leave the body rapidly, they are not usually associated with harmful effects. Too much exposure to tin compounds can cause stomachaches, blood changes, liver and kidney effects, and skin and eye irritation (32). Children playing at NHPC were exposed to tin in surface water and sludge on site. No specific populations unusually susceptible to health effects of inorganic tin compounds have been identified. ATSDR does not have MRLs for tin. EPA's RfD for tin ingestion is 0.62 mg/kg/day (32). The estimated doses of the children's tin exposure were well below the RfD; therefore, illness or injury are not expected.
Zinc
Zinc, one of the most abundant trace metals in humans, is found in all tissues and tissue fluids and is part of many enzyme systems (33). Children were exposed to zinc at NHPC in surface water, dried sludge, and soil on site. The children's estimated exposure to zinc in the lagoon sludge was lower than the RfD comparison values for ingestion of zinc. Therefore, no illness or injury from exposure to the estimated dose is expected.
Many different metals and nutrients affect the absorption, distribution, and excretion of zinc. Information about interactions resulting in increased zinc toxicity or increased toxicity of other substances in the presence of zinc was not found (33).
Cyanides
Cyanides are compounds composed of a common structure, which is formed when elemental nitrogen and carbon are combined. They are produced by certain bacteria, fungi, and algae and are found in many foods and plants. Of the cyanide compounds, hydrogen cyanide, sodium cyanide, and potassium cyanide are those most likely to be found in the environment as a result of industrial activities. Cyanide salts and hydrogen cyanide are used in electroplating (24). Cyanide is a powerful and rapid-acting poison. Exposure to high levels (1.52 mg/kg) for a short time damages the brain, lungs, and heart, and may cause coma and death. Cyanide's effects, regardless of exposure route, are similar after inhalation, ingestion, or skin contact (34).
Children playing at NHPC were exposed to cyanide in surface water and sludge. Although the exact half-life of cyanide in water is not known, it is believed to be short (24). Most cyanides in water form hydrogen cyanide and evaporate. Some cyanides in water are transformed into less harmful chemicals by microorganisms in the water or by forming a complex with metals, such as iron. ATSDR does not have MRLs for cyanide ingestion. The estimated dose of cyanide to which children playing on the site were exposed does not exceed the chronic oral RfD of 0.02 mg/kg/day. No data indicate that cyanides are carcinogenic. EPA has assigned cyanide a D classification, i.e., it is not possible to determine the potential of cyanide to cause cancer in people. The children's ingestion of cyanide at the estimated dose is not expected to cause illness or injury.
Carbon Tetrachloride (CCL4)
CCL4, a clear, heavy liquid with a sweet odor, evaporates readily; therefore, CCl4 is not often found in liquid form in the environment. Most CCl4 is found as a gas in the atmosphere. Small amounts also are found dissolved in water. In air, CCL4 concentrations of 0.1 ppb are common around the world; higher concentrations (0.2 to 0.6 ppb) are found in cities (35). Children at the NHPC site were exposed to CCl4 as a result of ingesting surface water and contacting (skin) surface water on the site. The acute oral MRL for CCL4 is 0.2 mg/kg/day; the intermediate MRL is 0.007 mg/kg/day (35). ATSDR does not have a chronic MRL; EPA's RfD is 0.0007 mg/kg/day. The estimated dose of children who contacted surface water containing CCl4 does not exceed either the MRLs or the RfD. Hence, no non-carcinogenic adverse health effects are expected after exposure at the estimated doses to CCL4 at the site.
Although CCL4 is classified by the EPA as a Group B2 probable human carcinogen, the estimated exposure to this compound is expected to result in a negligible increase in carcinogenic risk.
1,2-Dichloroethane (1,2-DCE)
1,2-DCE, a clear, synthetic liquid not found naturally in the environment, evaporates at room temperature; it has a pleasant smell and sweet taste. Small amounts of 1,2-DCE released into water or onto soil first evaporate into the air. Since it is readily broken down by sunlight, 1,2-DCE does not stay in the air very long. 1,2-DCE remaining on soil after a spill or improper disposal can move through the ground into water; it can remain in water or soil for long periods. ATSDR does not have intermediate and chronic MRLs for ingestion of 1,2-DCE; the acute MRL is 0.005 mg/kg/day (36). The estimated dose of 1,2-DCE to which people may have been exposed in surface water was less than the acute MRL. Neither illness or injury is expected following acute exposure to 1,2-DCE at the estimated dose.
1,1,1-Trichloroethane (1,1,1-TCA)
1,1,1-TCA is a colorless synthetic chemical. In the environment, it can be a liquid or a vapor, or exist dissolved in water and other chemicals. It also may exist as a liquid in soil and as a vapor in air. 1,1,1-TCA has a sweet yet sharp odor. Animal studies have not shown that 1,1,1-TCA in the air or water causes cancer or affects reproduction; however, some studies are not complete. Swallowing large amounts of 1,1,1-TCA has caused liver damage and death in animals and could be harmful to humans. EPA has assigned 1,1,1-TCA a carcinogenic classification of D, i.e., it cannot be classified with regard to whether it causes cancer in humans.
There are no MRLs or RfDs for 1,1,1-TCA, but because 1,1,1-TCA levels in NHPC surface water were very low, any ingestion by children playing on the site would have been negligible. Therefore, exposure at the dose estimated to have existed at NHPC would not be expected to cause illness or injury.
Trichloroethene (TCE)
TCE is a nonflammable, colorless liquid at room temperature with an odor similar to ether or
chloroform. The nervous system is probably most susceptible to illness or injury as a result of
chronic TCE exposure. TCE exposure at the NHPC site occurred by way of ingestion and by
skin contact with surface water. The most recent monitoring study at NHPC found levels of 0.04
ppm in surface water and 0.03 ppm in groundwater. ATSDR has derived an intermediate MRL
for TCE ingestion of 0.1 mg/kg/day, using what is known about TCE's ability to cause liver
damage. An EPA workgroup is reviewing the oral reference dose (RfD) for TCE. EPA
classified TCE as B2, a potential human carcinogen, i.e., TCE has caused cancer in one animal
species; that classification has since been withdrawn pending further review. The estimated dose
of TCE from surface water believed to have existed at NHPC is much lower than the
intermediate MRL. Therefore, no non-carcinogenic adverse health effects are anticipated as a
result of this type of exposure. Carcinogenic risk from this type of TCE exposure is expected to
be negligible.
Table 14.Comparison of Estimated Exposure Dose of Children Playing on Site to Health
Guidelines
Contaminant | Exposure Pathway | Health Guideline for Ingestion (mg/kg/day) | ||
Value | Source | Exceeded by Estimated Exposure Dose? | ||
Cadmium | Lagoon Surface Water | 0.0007 | Chronic Oral MRL | No |
Cadmium | Sludge | 0.0007 | Chronic Oral MRL | Yes |
Cadmium | Surface Soil | 0.0007 | Chronic Oral MRL | No |
Chromium (VI) | Surface Water | 0.005 | Chronic Oral RfD Cr(VI) |
No |
Chromium-Total | Surface Water | 0.005/ 1.00 | Chronic Oral RfD Cr(VI)/Cr(III) |
No/No |
Chromium Total | Sludge | 0.005/ 1.00 | Chronic Oral RfDCr(VI)/Cr(III) |
No/No |
Chromium Total | Soil | 0.005/ 1.00 | Chronic Oral RfD Cr(VI)/Cr(III) |
No/No |
Lead | Sludge depth unknown | NA | NA | NA |
Lead | Sludge | NA | NA | NA |
Lead | Soil | NA | NA | NA |
Nickel | Surface Water | 0.02 | Chronic Oral RfD | No |
Nickel | Sludge | 0.02 | Chronic Oral RfD | No |
Tin | Surface Water | 0.62 | Oral RfD | No |
Tin | Sludge | 0.62 | Oral RfD | No |
Zinc | Surface Water | 0.3 | Oral RfD | No |
Zinc | Sludge | 0.3 | Oral RfD | No |
Zinc | Soil | 0.3 | Oral RfD | No |
Cyanide | Surface Water | 0.02 | Chronic Oral RfDa | No |
Cyanide | Sludge | 0.02 | Chronic Oral RfDa | No |
CCl4 | Surface Water | 0.2 0.007 |
Acute MRL Inter. MRL |
No No |
1,2-DCE | Surface Water | 0.02 | Chronic Oral RfD | No |
TCE | Surface Water | 0.7 | Inter. MRL | No |
a = Free Cyanide and Hydrogen Cyanide
NA = Not available
Children at the Former Avanti Day Care Center
Children at the Former Avanti day care center were occasionally exposed to cyanide and cadmium during site remediation. Exposure was by way of inhalation.
Cyanide
As reported earlier in this public health assessment, cyanide was detected in ambient air three times at the day care center monitoring station; the maximum concentration measured was 0.026 mg/m3. There are no MRLs for acute, intermediate, or chronic exposure to cyanide by way of inhalation; similarly, EPA has no RfDs for cyanide. At least nine states, however, have regulations and/or guidelines for acceptable ambient air concentrations of cyanide and its derivatives (34). The amount of cyanide detected at the day care center is well below the lowest reported state regulation (0.1 mg/m3 for a 1-hour exposure, 0.2 mg/m3 for an 8-hour exposure, and 0.08 mg/m3 for a 24-hour exposure). It is unlikely that cyanide exposure at those concentrations could cause illness or injury.
Cadmium
Cadmium was also detected in ambient air at the day care monitoring station (maximum
concentration: 0.0003 mg/m3) (Table 15). Although the maximum concentration detected
exceeds the chronic MRL, cadmium was detected only once in the ambient air around the day
care center probably as a result of ongoing remedial activities at the time. Based on this data, no
adverse health effects are anticipated to result from cadmium exposure of children at the Avanti
Day Care Center.
Table 15.Comparison of Estimated Exposure Doses of Children at the Day Care Center to
Health Guidelines
Contaminant | Exposure Pathway | Health Guideline (mg/m3) | ||
Value | Source | Exceeded by Estimated Exposure Dose? | ||
Cadmium | Off-site Ambient Air |
0.0002 | Chronic Inhal. MRL |
Yes |
Cyanidea | Off-site Ambient Air |
NA | NA | NA |
a There are no health guidelines for comparison with estimated exposure doses.
NA = Not available
Workers at NHPC
Workers at the NHPC site were exposed to cadmium, chromium, zinc, nickel, and tin (Table 16). Before operations ceased in 1985, exposure to contaminants occurred by way of ingestion of dust and other small particles over an estimated 20 year period beginning in 1962. To estimate ingestion exposure, it was assumed that the typical worker ingested about 200 mg of dust/day during 260 days of exposure over the course of a year. Indoor air monitoring data were not provided to ATSDR; as a result, an estimated inhalation dose could not be calculated.
Cadmium
Workers who inhale cadmium for a long period (chronic inhalation) may have an increased chance of developing lung cancer (27). The estimated exposure dose of adults working in the facility exceeded ATSDR's chronic ingestion MRL of 0.0002 mg/kg/day. Since the estimated exposures were high, those persons may have experienced (and may continue to experience) illness or injury, although none have been reported to ATSDR. Proteinuria, kidney tubule dysfunction, and reduced urine are some expected effects of exposure (27). Cigarette smoke exposes the general population to higher than average levels of cadmium. Smokers with occupational exposure to cadmium are at highest risk for illness or injury. Although cadmium is classified as a probable carcinogen when exposure is by way of inhalation, neither human nor animal studies provide sufficient evidence to determine whether cadmium causes cancer when exposure is oral.
Chromium
NHPC workers were exposed to chromium by ingesting dusts and other small particles at the facility. More data are available on the effects of chronic inhalation exposure in people and animals than there are on the effects of oral exposure. ATSDR was not provided with data on chromium concentrations in air inside NHPC. The respiratory system and the skin are the primary target organs for occupational exposure to chromium and its compounds (28).
The literature did not report any target organ toxicity in animals from chronic oral exposure to chromium (III) and chromium (VI) compounds. This lack of toxicity may have been because of the poor absorption of chromium through the gastrointestinal tract. The estimated exposure dose of chromium of workers at the NHPC facility exceeded the chronic RfD for ingestion of chromium (VI). However, exposure at the estimated doses is not expected to cause illness or injury, except in chromium sensitive sub-populations. In that population, skin irritation is expected. Chromium is classified as a human carcinogen, and occupational inhalation studies indicate a correlation between long-term exposure to chromium (VI) compounds and lung cancer. Occupational studies generally are concerned with inhalation exposures. Cancer studies have shown that chronic inhalation of chromium (VI) compounds is carcinogenic in mice. Conversely, chronic oral exposure to chromium (VI) did not have significant carcinogenic effects (28).
Although there are no data on indoor air quality at NHPC, it can be assumed that workers were exposed to chromium by way of inhalation. Lung cancer may occur long after exposure has ended. It is not clear which form(s) of chromium cause lung cancer in workers. Chromium (VI) is believed to be primarily responsible for increased lung cancer rates in workers exposed to high levels of chromium in air. Occupational exposure to chromium (III) compounds may not be as great a concern as chromium (VI) exposure. Oral exposure to chromium is not believed to cause cancer.
Nickel
Workers were exposed to nickel inside the NHPC facility. Cancer of the lung and nasal sinus is the most serious effect of chronic nickel exposure in humans, but it also effects the heart, blood, and kidneys, and may cause allergic reactions. The literature reports an increased death rate from lung diseases in people who inhaled nickel while working (31). An increased rate of cancers of the lung and the nose were also observed in workers exposed to nickel. EPA classifies nickel refinery dust and nickel subsulfide as Group A human carcinogens while nickel carbonyl is classified as a Group B2 carcinogens.
ATSDR does not have MRLs for nickel ingestion. EPA's RfD (oral) for soluble nickel compounds is 0.02 mg/kg/day. The estimated dose of nickel ingested by workers at NHPC, however, is much less than the RfD and should not cause non-carcinogenic adverse health effects.
Tin
Workers at the NHPC facility also were exposed to tin by ingesting dust and other small particles. ATSDR does not have MRLs for tin ingestion. EPA's oral RfD for inorganic tin is 0.62 mg/kg/day. The estimated exposure dose for workers at the NHPC facility was much less than that value, therefore, neither illness nor injury is expected.
Zinc
Workers also were exposed to zinc inside the NHPC facility. No relationship between the
occurrence of cancer in humans and occupational exposure (primarily by way of inhalation) to
zinc has been demonstrated (33). No data were available on respiratory effects in people or
animals following oral exposure to zinc or zinc compounds. Several studies have suggested that
ingestion of zinc may cause symptoms of gastrointestinal distress or alterations in
gastrointestinal tissues (33). The type of zinc compound at the NHPC facility is unknown;
however, the estimated ingestion dose of zinc at NHPC does not exceed the RfD comparison
value of 0.3 mg/kg/day; therefore, no illness or injury is expected.
Table 16.Comparison of Estimated Exposure Dose of NHPC Workers to Health Guidelines
Contaminant | Exposure Pathway (Ingestion) |
Health Guideline (mg/kg/day) | ||
Value | Source | Exceeded by Estimated Exposure Dose? | ||
Cadmium | Dust/Small particles | 0.004 0.0007 |
Acute MRL Chronic Oral MRL |
Yes Yes |
Chromium | Dust/Small particles | 0.005 | Chronic Oral MRL | Yes |
Zinc | Dust/Small particles | 0.3 | Oral RfD | No |
Nickel | Dust/Small particles | 0.02 | Chronic Oral RfD |
No |
Tin | Dust/Small particles | 0.62 | Oral RfD | No |
Recreators at Horseshoe Pond/Merrimack River
Sediment and Surface Water
Exposure to Merrimack River surface water and sediment contaminant levels in areas proximal to the site is not expected to result in adverse health effects. Concentrations of VOCs, metals and cyanide in Merrimack River surface water and sediment were either below detection or within the range of normal background.
Exposure to Horseshoe Pond sediment and surface water is not expected to results in any adverse health effects. Current levels of site related contaminants are either below detection or within the range of normal background. Maximum concentrations of cadmium (2 ppb) and cyanide (580 ppb) detected in Horseshoe Pond surface water during 1982 sampling are not expected to cause adverse health effects for recreators who have used the pond in the past.
Fish
Based on surface water and sediment sampling data, fish in the Horseshoe Pond and Merrimack River are not expected to bioaccumulate site related contaminants. However, it should be noted that NHDPHS has issued a Fish Ingestion Advisory for Horseshoe Pond based on elevated mercury levels in found in largemouth bass. The elevated mercury levels detected in Horseshoe Pond fish are not thought to be related to the NHPC site.
Private Well Users
Residents who use water from the private well on Daniel Webster Highway were exposed to 1,1-dichloroethane, 1,1-dichloroethene (DCE), 1,1,2,2-tetrachloroethane, 1,1,1-trichloroethane tetrachloroethene (PCE), and trichloromethane (chloroform) by way of inhalation, ingestion and/or dermal contact. Available MRLs and RfDs which are listed below for these VOCs were not exceeded and thus no non-carcinogenic adverse health effects are anticipated to result from the use of this well.
Based on the March, 1990 sample of this private well, an ATSDR Health Consultation concluded that no adverse health effects would result from use of this well. An additional sample taken in August, 1993 detected similar VOC contamination with some VOCs detected at higher levels than the previous sample. Although VOC levels detected in this more recent sampling are still not expected to result in non-carcinogenic adverse health effects, the continued presence of multiple carcinogenic VOCs at the levels detected indicate a low increase in carcinogenic risk. This prompted NHDPHS to recommend that the well not be used for drinking purposes and that showering use be minimized (43).
B. Health Outcome Data Evaluation
Health outcome data were not evaluated for this site because the population of concern (50-75
residents) is very small. As a result, it would be very unlikely that any health effects associated
with the site could be detected. No previous health studies on the population near the NHPC site
were identified during the gathering of data for this public health assessment, and no community
concerns were expressed about possible health outcomes.
Table 17.Comparison of Estimated Exposure Dose of Private Well Users to Health
Guidelines
Contaminant | Exposure Pathway (Ingestion) |
Health Guideline (mg/kg/day) | ||
Value | Source | Exceeded by Estimated Exposure Dose? | ||
1,1-dichloroethane | Private Well | NA | NA | NA |
DCE | Private Well | 0.20 0.009 |
Inter. MRL Chronic MRL |
No No |
1,1,2,2-Tetrachloroethane | Private Well | NA | NA | NA |
1,1,1-trichloroethane | Private Well | NA | NA | NA |
PCE | Private Well | 0.1 0.01 |
Inter. MRL Oral RfD |
No No |
chloroform | Private Well | 0.01 | chronic MRL | No |
NA = Not available
C. Community Health Concerns Evaluation
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