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PUBLIC HEALTH ASSESSMENT

CARTER-LEE LUMBER COMPANY
INDIANAPOLIS, MARION COUNTY, INDIANA



ENVIRONMENTAL CONTAMINATION AND OTHER HAZARDS

The tables in this section list the contaminants of concern. We evaluate these chemicals and present our findings in subsequent sections of this public health assessment. We determine whether exposure to the chemicals has occurred, and if so, we discuss the public health significance of those exposures. ATSDR selects and discusses a chemical as a contaminant of concern based upon the following factors:

  1. comparison of on-site and off-site contaminant concentrations with contaminant concentrations for environmental media derived from values used to evaluate noncarcinogenic and carcinogenic health endpoints;

  2. no comparison value exists for the contaminant in an environmental medium and the toxic properties are not known;

  3. an evaluation of the field data quality, laboratory data quality, and sample design; and

  4. community health concerns related to a particular chemical.

In the data tables presented in the On-Site Contamination and Off-Site Contamination subsections, the listed chemical does not mean that it will cause adverse health effects because it is present above a comparison value. Instead, the list indicates which chemicals are evaluated further.

The ATSDR definition of subsurface soil is: any soil sample collected at 3 inches or deeper. In contrast the definition of subsurface soils reported in the RI is 6 inches or greater. The data tables in this document reflect the ATSDR definition. We evaluated the sample data reported in the final RI report.

Data tables include the following acronyms:

CREG = Cancer Risk Evaluation Guide. CREGs are estimated contaminant concentrations based on one excess cancer in a million people exposed over a lifetime. They are calculated from EPA's cancer slope factors.
EMEG = Environmental Media Evaluation Guide. EMEGs are media-specific comparison values that are used to select chemicals of concern at hazardous waste sites. They are derived from the minimal risk level.
LTHA = Lifetime Health Advisory (for drinking water). The LTHA is derived from the Drinking Water Equivalent Levels (DWEL) for noncarcinogens. For noncarcinogenic organic and inorganic compounds, LTHAs are 20% and 10%, respectively, of the DWEL. For possible carcinogens, the LTHA is divided by an additional factor of 10.
MCL = Maximum Contaminant Level (for drinking water). MCLs represent contaminant concentrations that EPA deems protective of public health (considering the availability and economics of water treatment technology) over a lifetime (70 years) at an exposure rate of 2 liters of water per day. While MCLs are regulatory concentrations, Proposed Maximum Contaminant Level Goals and Maximum Contaminant Level Goals are not.
NAS = National Academy of Sciences. NAS determined that water supplies containing more than 20 ppm sodium may pose problems for people who are on sodium-restricted diets of 1 gram per day.
ppm = Parts per million.
ppb = Parts per billion.
RfD = Reference Dose. EPA's estimate of the daily exposure to a contaminant that is unlikely to cause noncancer adverse health effects.
RMEG = Reference Dose Media Evaluation Guide. RMEGs are media-specific comparison values that are used to select chemicals of concern at hazardous waste sites. They are derived from the reference dose.

The Toxic Chemical Release Inventory (TRI) is an EPA database that contains information on chemical releases from industries in the United States. It is used to determine the potential sources of contamination near NPL sites. The TRI includes only chemical releases that have been reported since the database was initiated in 1987. A computer search was conducted by zipcode (46222) of all available toxic release inventory (TRI 87-93) data to determine the number of industries within this zipcode that potentially emit chemicals into the environment which are in common with the Carter-Lee Lumber Company site.

The TRI listed eight facilities within this zipcode which emit the following chemicals into the air: ammonia, nitric acid, phosphoric acid, sodium hydroxide, sulfuric acid, 1,1,1-trichloroethane, tetrachloroethane, aluminum oxide, and cobalt. No water or land emissions were reported for those chemicals.

EPA conducted a remedial investigation in two phases between November 1992 (Phase I) and June/September 1993 (Phase II).

Phase I sampling was conducted for on-site surface soil (CLSS01-03), on-site soil boring (CLSBO1-12), off-site subsurface soil (CLBK01-02, 07-17), on-site groundwater (CLMW01, 03, 04, 05), off-site groundwater (CLMW02), and off-site (upgradient) groundwater (CLMW01). Subsurface soil sample CLBK02 was collected from a garden at a single residence.

Phase II focused on off-site subsurface soil (CLBK03 & CLBK06) and off-site groundwater (CLMW02) monitoring.

A. On-Site and Off-Site Soil Samples

On-site subsurface soil samples (see Figure 2) were analyzed for volatile organic compounds (VOCs), semi-volatile organic compounds (SVOCs), pesticides, polychlorinated biphenyls (PCBs), inorganic chemicals, and cyanide. Phase I (November 1992), on-site soil boring samples were analyzed for VOCs, SVOCs, pesticides, PCBs, inorganic chemicals, and cyanide. The results of the analyses are summarized in Table 1.

Off-site subsurface soil samples (see Figure 3) were analyzed for SVOCs and inorganic chemicals. Because the four primary samples of the off-site analyses were for inorganic chemicals and polycyclic aromatic hydrocarbons (PAHs) only, selected samples were analyzed for VOCs, pesticides, PCBs, and cyanide. All chemicals that were detected off site at a level exceeding comparison values are listed in Table 1.

In addition, two off-site subsurface soil samples (CLBK03 & 06; see Figure 3) were collected during Phase II (June/September 1993). Off-site subsurface soil samples were analyzed for VOCs, SVOCs, pesticides, PCBs, inorganic chemicals, and cyanide. All off-site chemicals that were detected at a level above comparison values during the June/September 1993 sampling are listed in Table 2.

B. Groundwater Samples

On- and off-site groundwater samples were analyzed for VOCs, SVOCs, pesticides, PCBs, inorganic chemicals, and cyanide. In November 1992, Phase I results identified the presence of 15 inorganic chemicals in on-site groundwater samples and 8 inorganic chemicals in off-site groundwater samples.

In June and September 1993, during Phase II, two additional rounds of on- and off-site groundwater collection and analyses were conducted (see Figure 4). In addition, two off-site subsurface soil samples (CLBK03, 06) were collected.

On- and off-site groundwater samples were analyzed for VOCs, SVOCs, pesticides, PCBs, inorganic chemicals, and cyanide. In June and September 1993, Phase II results identified the presence of 3 inorganic chemicals in on-site groundwater samples and 3 inorganic chemicals in off-site groundwater samples. All chemicals that were detected in on- and off-site groundwater at a level of concern are listed in Table 3.

Figure 2
Figure 2. On-Site Soil Sample Location Map

Figure 3
Figure 3. Off-site Soil Sample Location Map



Table 1. Phase I On- Site and Off-Site Soil Sample Results, November 1992

Chemical On-site Sampling Off-site Sampling Comparison Value
Depth 0 - 18 Feet Depth 0 - 20 Feet Depth 0 -16 Feet
Sample
Location
Sample
Depth
(Feet)
Maximum
Concentration
Range (ppm)
Sample
Location
Sample
Depth
(Feet)
Maximum
Concentration
Range (ppm)
Sample
Location
Sample
Depth
(Feet)
Maximum
Concentration
Range (ppm)
ppm Source
aluminum CLSS03 & CLSS01 1 - 18 3,030 - 5,510 CLSB12 & CLSB05 0 - 10 2,310 -
14,900
CLBK13 & CLBK14 0 - 0.5 2,820 - 16,000 0.8 RMEG
antimony - - - CLSB7,8,9 & CLSB05 0 - 4 3.5 - 10 - - - 0.8 RMEG
arsenic CLSS01 & CLSS03 0 - 18 12.8 - 14.4 CLSB09 & CLSB05 0 - 4 6.6 - 197 CLBK15 & CLBK17 0 - 0.5 4 - 59.5 0.6 EMEG
barium CLSS03 & CLSS01 0 - 18 20.9 - 63 CLSB08 & CLSB11 0 - 5 1.2 - 158 CLBK13 & CLBK14 0 - 0.5 14.9 - 198 100 RMEG
benzo(a)anthracene CLSS02 & CLSS03 0 - 18 0.71 - 0.79 CLSB01 & CLSB11 0 - 20 0.4 - 2.4 CLBK12 & CLBK09 0 - 0.5 0.5 - 360 * -
benzo(a)pyrene CLSS03 0 - 18 0.71 CLSB01 & CLSB11 0 - 20 0.39 - 2.1 CLBK12 & CLBK09 0 - 0.5 0.48 - 360 0.1 CREG
benzo(b)fluoranthene CLSS03 & CLSS02 0 - 18 0.68 - 1.6 CLSB01 & CLSB04,11 0 - 20 0.47 - 2.4 CLBK13 & CLBK09 0 - 0.5 0.38 - 290 * -
benzo(g,h,i)perylene CLSS02 0 - 1 0.53 CLSB07 0 - 2 1.4 CLBK15 & CLBK09 0 - 0.5 1.2 - 140 * -
benzo(k)fluoranthene CLSS03 0 - 18 0.61 CLSB11 3 - 5 2 CLBK11,12 & CLBK09 0 - 0.5 0.45 - 290 * -
beryllium CLSS02 & CLSS01 0 - 1 0.36 - 0.48 CLSB12 & CLSB08 0 - 10 0.29 - 151 CLBK04,13 & CLBK12 0 - 0.5 0.25 - 1.2 0.2 CREG
cadmium CLSS02 & CLSS03 0 - 18 0.89 - 1.2 CLSB10 & CLSB04,12 0 - 16 0.07 - 0.9 CLBK13 & CLBK09 0 - 0.5 0.85 - 5.6 1 EMEG
calcium CLSS02 0 - 1 102,000 CLSB05 & CLSB10 0 - 16 4,460 - 198,000 - - - * -
carbazole - - - - - - CLBK15 & CLBK16 0 - 0.5 0.37 - 1.2 * -
chromium CLSS02 0 - 1 11.2 CLSB04 & CLSB10 2 - 16 10.2 - 439 CLBK01 0 - 16 10.2 10 RMEG
chrysene CLSS03 & CLSS02 0 - 18 0.74 - 0.8 CLSB01 & CLSB11 0 - 20 0.39 - 2.6 CLBK13 & CLBK11 0 - 0.5 0.4 - 0.79 * -
cobalt CLSS02 & CLSS01, CLSS03 0 - 18 4 - 4.4 CLSB12 & CLSB10 0 - 10 3.3 - 15.3 CLBK13 & CLBK02** 0 - 0.5 3.3 - 16.3 * -
copper CLSS02 & CLSS01 0 - 1 22 - 25.6 CLSB11 & CLSB05 0 - 5 17.2 - 114 CLBK13 & CLBK04 0 - 0.5 13.2 - 6,970 * -
dibenz(a,h)anthracene - - - - - - CLBK15 & CLBK10 0 - 0.5 0.5 - 1.3 * -
dibenzofuran - - - - - - CLBK16 0 - 0.5 0.45 * -
fluoranthene CLSS02 & CLSS03 0 - 18 0.99 - 1.4 CLSB10 & CLSB11 2 - 6 0.65 - 5 CLBK02** & CLBK09 0 - 0.5 0.37 - 790 80 RMEG
indeno(1,2,3-cd)pyrene CLSS03 0 - 18 0.4 CLSB03 & CLSB11 0 - 18 0.36 - 0.97 CLBK12 & CLBK10 0 - 0.5 0.4 - 2.9 * -
iron CLSS02 0 - 1 8,860 CLSB12 & CLSB05 0 - 10 6,510 - 161,000 CLBK01 0 - 16 12,900 * -
lead - - - CLSB07 & CLSB08 0 - 2 18.4 - 376 - - - * -
magnesium CLSS03 & CLSS01 0 - 18 27,800 - 50,100 CLSB10 & CLSB09 0 - 6 605 - 25,100 CLBK07 & CLBK04 0 - 0.5 4,080 - 39,400 * -
manganese CLSS03 & CLSS01 0 - 18 275 - 404 CLSB09 & CLSB06 0 - 4 314 - 1,280 CLBK04 & CLBK02** 0 - 0.5 276 - 1,400 300 RMEG
2-methyl naphthalene - - - - - - CLBK17 0 - 0.5 0.42 * -
nickel CLSS03 & CLSS01 0 - 18 9.9 - 14.1 CLSB12 & CLSB07 0 - 10 9.5 - 173 CLBK13 & CLBK14 0 - 0.5 7 - 33.3 40 RMEG
phenanthrene CLSS02 & CLSS03 0 - 18 0.75 - 1.1 CLSB01 & CLSB09 0 - 20 0.41 - 2.8 CLBK01,14 & CLBK09 0 - 16 0.5 - 370 * -
potassium CLSS02 & CLSS01 0 - 1 465 - 775 CLSB10 & CLSB05 0 - 6 169 - 1,250 CLBK09 & CLBK14 0 - 0.5 511 - 2,130 * -
pyrene CLSS02 & CLSS03 0 - 18 0.99 - 1.8 CLSB06 & CLSB04 0 - 16 0.63 - 2.6 CLBK13 & CLBK09 0 - 0.5 0.4 - 800 60 RMEG
sodium CLSS03 & CLSS01 0 - 18 103 - 139 CLSB10 & CLSB08 0 - 6 29.3 - 197 CLBK07 & CLBK14 0 - 0.5 47.9 - 1,510 20 NAS
thallium - - - CLSB07,08,09 & CLSB10 0 - 6 0.11 - 0.36 CLBK13 & CLBK17 0 - 0.5 0.21 - 0.45 * -
vanadium CLSS03 & CLSS01 0 - 18 9.7 - 164 CLSB10 & CLSB05 0 - 6 5.3 - 88.6 CLBK13 & CLBK14 0 - 0.5 10.5 - 45.9 6 EMEG

* No comparison value available
**Sample # CLBK02 is a sample taken from a garden.
Single concentration indicates that only one sample was collected.
- Indicates that no sample was analyzed for that contaminant.


Table 2. Phase II Off-site Subsurface Soil Sample Results (Depth 0 - 1 Foot), June/September 1993

Chemical Sample Location Sample
Depth
Maximum
Concentration
Range (ppm)
Comparison Value
ppm Source
aluminum CLBK03 & CLBK06 0 - 1 3.58 - 4.94 * -
benzo(a)anthracene CLBK06 & CLBK03 0 - 1 0.44 - 1.2 * -
benzo(a)pyrene CLBK06 & CLBK03 0 - 1 0.44 - 1.9 0.1 CREG
benzo(b)fluoranthene CLBK06 & CLBK03 0 - 1 1.2 - 4 * -
benzo(g,h,i)perylene CLBK03 0 - 1 0.99 * -
benzo(k)fluoranthene CLBK06 & CLBK03 0 - 1 0.73 - 2 * -
chrysene CLBK06 & CLBK03 0 - 1 0.67 - 1.8 * -
dibenz(a,h)anthracene CLBK03 0 - 1 0.4 * -
indeno(1,2,3-cd)pyrene CLBK03 0 - 1 1.2 * -
2-methyl naphthalene CLBK03 0 - 1 0.7 * -
naphthalene CLBK03 0 - 1 0.63 * -
phenanthrene CLBK06 & CLBK03 0 - 1 0.81 - 1.7 * -

Single concentration indicates that only one sample was collected
* No comparison value available
- Not applicable because no comparison value is available


Figure 4. Groundwater Monitoring Well Locations

Table 3. Phases I & II On-Site and Off-Site Groundwater Sample Results; November 1992, June 1993, and September 1993

Chemical On-site Sampling Off-site Sampling (Upgradient) Comparison
Value
Sample
Location
Sample
Dates
Maximum
Concentration
Range (ppb)
Sample
Location
Sample
Dates
Maximum
Concentration
Range (ppb)
ppb Source
aluminum CLMW03 & CLMW01 11/92 26,500 - 32,300 - - - 4 RMEG
arsenic CLMW04 & CLMW05 11/92 1,100 - 1,500 CLMW02 11/92 1,600 3 EMEG
barium CLMW04 & CLMW05 11/92 44,800 - 68,500 CLMW02 11/92 67,000 700 RMEG
beryllium CLMW03 11/92 1,100 - - - .008 CREG
calcium CLMW01 & CLMW05 09/93 & 11/92 116,000 - 19,700,000 CLMW02 09/93 101,000 * -
iron CLMW03 & CLMW04 11/92 10,600 - 23,500 - - - * -
lead CLMW03, CLMW05 & CLMW01 11/92 1,200 - 1,400 CLMW02 06/93 5.5 15 MCL
magnesium CLMW05 & CLMW04 06/93 & 11/92 28,200 - 40,200,000 CLMW02 06/93 31,400 * -
manganese CLMW01 & CLMW05 09/93 & 11/92 27 - 90,600 CLMW02 11/92 7,800 50 RMEG
nickel CLMW03 & CLMW05 11/92 8,900 - 11,400 CLMW02 11/92 11,400 200 RMEG
potassium CLMW01 & CLMW04 11/92 3,840,000 - 4,490,000 CLMW02 11/92 4,400,000 * -
selenium CLMW03 & CLMW05 11/92 1,300 - 3,700 CLMW02 11/92 3,000 20 EMEG
sodium CLMW05 & CLMW04 11/92 24,800,000 - 53,200,000 CLMW02 11/92 31,200,000 20 NAS
thallium CLMW03 11/92 1,000 CLMW02 11/92 1,400 0.4 LTHA
zinc CLMW03 11/92 4,600 - - - 3,000 RMEG

Single concentration indicates only one sample
* No health comparison value available
- Not applicable because no comparison value exists

No surface water or ambient air monitoring were conducted during the RI.

C. Quality Assurance and Quality Control (QA/QC)

Data from the sampling events used in the preparation of this report were reviewed, and they fulfilled the requirements for QA/QC. All duplicates, blanks, reference standards, associated retention times, matrix spike and matrix spike duplicates, and surrogate detection limits were met.

No estimated or qualified values were used in the preparation of this report.

D. Physical and Other Hazards

The Carter-Lee Lumber Company presently uses the area of contamination for temporary lumber storage. The piles of lumber present a trip and fall hazard; however, this area is restricted by a 8-foot fence and personnel working in this area are aware of the hazards of working around piles of lumber.


PATHWAYS ANALYSES

To determine whether nearby residents are exposed to contaminants migrating from the site, ATSDR evaluates the environmental and human components that lead to human exposure. An exposure pathway consists of five elements: 1) a source of contamination, 2) transport of contaminants through an environmental medium, 3) a point of exposure, 4) a route of human exposure, and 5) an exposed population.

ATSDR categorizes exposure pathways as complete, potential, or eliminated. All five pathway elements are present in completed pathways. The exposure either occurred in the past, is occurring, or will occur in the future. If at least one of the five elements is missing, the exposure pathway is potential if the missing element is likely to exist, but we do not have data to substantiate the missing element. Exposure to a contaminant could have occurred in the past, could be occurring, or could occur in the future. An exposure pathway can be eliminated if at least one of the five elements is missing and will never be present. No completed exposure pathways were identified. Table 4 identifies potential exposure pathways. The discussion that follows Table 4 incorporates only those pathways that are important and relevant to the site.

A. Completed Exposure Pathways

We did not identify any completed human exposure pathways.

B. Potential Exposure Pathways

On-site and off-site groundwater

Residents in this area use a municipal water supply that is monitored according to federal regulations. No municipal wells are within a 1-mile radius of the site. The closest drinking water well is approximately 3,500 feet away, west of and upgradient from the site. However, on-site monitoring wells contain very high levels of lead and arsenic.

Marion County occasionally supplements its municipal supply with groundwater pumped from the same aquifer monitored at the site. This well field is approximately 7 miles south of the site and should not be influenced by site contaminants.

If people used old, existing private wells on or in the near vicinity of the site, those people could be exposed to site-related contaminants through direct ingestion or dermal contact. People may have used those wells in the past, but we do not know what levels of contaminants may have been present when the wells may have been used. Furthermore, if the wells did exist, they were likely abandoned and would be difficult to locate for testing. Additionally, we would not know if contaminants that may be present today reflect what may have been in the well water when they were used. People are not using the wells presently but could use the wells in the future if allowed.

Eleven industrial wells were identified downgradient of the site. The well owners surveyed have wells screened in the same aquifer sampled on site. We believe that the industries use municipal water for their drinking water supply and only use their industrial wells for industry processes. Those workers are not believed to be exposed to site-related contaminants.


Table 4. Potential Exposure Pathways

PATHWAY
NAME
EXPOSURE PATHWAY ELEMENTS TIME
SOURCE ENVIRONMENTAL
MEDIA
POINT OF
EXPOSURE
ROUTE OF
EXPOSURE
EXPOSED
POPULATION
Groundwater Carter-Lee
Lumber
Groundwater On Site
Off Site
Ingestion
Dermal Contact
Residents Past
Future

C. Eliminated Exposure Pathways

Although contamination exists in on-site subsurface soil, no one is expected to come into contact with that soil. The contaminated areas are covered with clean top soil, gravel, and asphalt.


PUBLIC HEALTH IMPLICATIONS

In this section, we discuss the health effects of people exposed to specific chemicals, evaluate state and local health databases, if available, and address any existing community health concerns.

A. Toxicological Evaluation

This subsection of the public health assessment describes the public health implications of exposure to contaminants that are associated with the site. ATSDR developed toxicological profiles for several chemicals that have been found at this site. These profiles provide information on health effects, environmental transport, human exposure, and regulatory status. No completed exposure pathways were identified; therefore, no one is expected to experience site-related adverse health effects. We did identify a potential exposure pathway through use of contaminated groundwater.

People may have been exposed to contaminants in the past through drinking contaminated water in on-site and nearby off-site wells. If allowed, people may use contaminated well water in the future. No one is using private well water for drinking or household purposes at the present time. Although a number of contaminants exceeded comparison values in groundwater, we will discuss only arsenic and lead because the toxicity of those two chemicals is better known. Should future investigations indicate that people are being exposed to contaminated groundwater, ISDH will further evaluate other contaminants in the water. Because a community member was concerned about contaminants in soil carried to their home for use in a garden, we did evaluate the garden soil for contaminants. We did not find any contaminants that exceeded comparison values in the garden soil. Therefore, people who garden at that home are not expected to experience any adverse health effects as a result of that activity.

Arsenic

Long-term oral exposure to inorganic arsenic may cause a pattern of skin changes. Skin changes include darkening of the skin and the appearance of small corns or warts on the palms, soles, and torso. While these skin changes are not considered to be a health concern, a small number of the corns may ultimately develop into skin cancer. Swallowing arsenic has also been reported to increase the risk of cancer of the liver, bladder, kidneys, and lungs (3).

Arsenic was found at 1,600 ppb and 1,500 ppb in the off-site and on-site groundwater, respectively. Possible health effects associated with ingesting the groundwater in this area are irritation of the stomach and intestines with symptoms such as pain, nausea, vomiting, and diarrhea (3).

Lead

Lead is found in the earth's crust as a naturally occurring metal. Because lead has been widely used, such as in leaded gasoline, lead is found in air, drinking water, rivers, lakes, oceans, dust, soil, and in animals and plants. Lead can enter the body through inhalation (lead dust), ingestion (lead contaminated foods), but only small portions will absorb through the skin (5).

Lead is partitioned first in the soft tissues (liver, kidneys, lungs, brain, spleen, muscles, and heart). After several weeks it travels to and is stored in bone and teeth. Symptoms associated with lead exposure at high levels include possible decrease in memory; weakness in the fingers, wrists, or ankles; and anemia (5).

Children are more sensitive to the effects of lead than adults. Lead exposure can cause premature birth, smaller babies, decreased intelligent quotient and damage to the male reproductive system in adults, and brain and kidney damage in both children and adults (5). We do not know how much lead will cause these effects, but the Centers for Disease Control and Prevention (CDC) recommends that children's blood lead levels not exceed 10 micrograms per deciliter (5).

Lead was found at 376 ppm in the on-site soil. Soil in this area of the United States typically contains 10-300 ppm of lead. The level found in the on-site soil is within guidelines for residential soils. Lead was found in the on-site groundwater at 1,400 ppb and 5.5 ppb in the off-site groundwater. EPA has established an Action Level for lead in public drinking water supplies at 15 ppb. That means if a public water supply contains lead at 15 ppb, then action must be taken to lower the level of lead. EPA's Maximum Contaminant Level Goal for lead is zero.

ATSDR has not derived a minimum risk level (MRL) for lead. A RfD does not exist for lead because no thresholds (safe levels) have been demonstrated. Therefore, ATSDR recommends that people avoid lead exposure whenever possible (5).

B. Health Outcome Data Evaluation

No completed exposure pathways have been identified. For that reason, no adverse health effects related to site contamination are expected, and no one has reported experiencing adverse health effects they feel may be a result of exposure. For those reasons, we did not evaluate any health outcome data.

C. Community Health Concerns Evaluation

  1. I took soil from the site for my garden. My children may have been exposed to this dirt. Should I be concerned?

    Soil samples taken from garden dirt showed very low levels of contaminants. In fact, the levels found are comparable to what is found in most urban soils. Several factors determine whether a contaminant in the environment will pose a health risk. A few of these factors include how much of the contaminant is there, how often a person is exposed to that level, and whether the person touches, breathes, or ingests the contaminant.

    We feel that young children likely ingest more soil than adults and older children because of their hand to mouth activities. For that reason, we use very conservative ingestion rates when we calculate how much of a contaminant a young child might ingest. Although the levels of contaminants in the soil in your garden are low, we feel you should continue to encourage healthy habits in your children such as washing of hands before eating. If you have very young children in your home, you may want to observe your children at play to determine any unusual play habits such as eating dirt. Some children have a rare condition called pica, which is a craving for unnatural things (dirt, clay, chalk), caused by lack of specific nutrients in the body. If you feel your child may have pica, you should consult with your family doctor.

  2. Is it safe to eat vegetables grown in soil taken from this site?

    Most contaminants do not readily accumulate in the edible portions of plants. The contaminants that are known to accumulate in edible plant tissue were not found in the garden soil sample at levels that would cause problems. For instance, a study of carrots grown in chemically contaminated soils indicated that small amounts of contaminants were found only in the peelings of the carrot and not in the interior of the root. Surface absorption appears to be the major means whereby certain chemicals accumulate in crops. In the carrot study, leaf samples contained only small amounts of contaminants, but scientists were not clear whether the contaminant found on the leaves was the result of uptake through the root system or from soil particles on the surface of the leaves (6). For that reason, we recommend that, regardless of where fruits and vegetables are grown, you wash your vegetables thoroughly and peel any root vegetables such as beets, carrots, radishes, and potatoes.

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