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' Human Health Screening Evaluation <br /> Surland Homes—Bridle Creek February 12,2009 <br /> incremental lifetime cancer risk; EPA, 1989). The potential carcinogenic health risks for each <br /> individual chemical in an exposure pathway were summed to estimate an overall cancer risk for <br /> each exposure pathway. Cancer risks across all evaluated exposure pathways were then summed <br /> to estimate incremental lifetime cancer risk for the individual. <br /> Potential future non-cancer health hazards were likewise calculated for on-site residential child <br /> ' receptors. Hazards were estimated by comparing estimated potential on-site doses to an <br /> acceptable reference-dose exposure. The calculated ratio of the potential estimated dose to the <br /> reference dose (the hazard quotient) was calculated for potential exposure to each COPC. The <br /> potential health hazards for each chemical in an exposure pathway were summed to estimate the <br /> total heath hazard for each exposure pathway. Health hazards across all evaluated exposure <br /> pathways were then summed to estimate the total hazard index for the receptor. <br /> In accordance with the National Contingency Plan, an incremental lifetime cancer risk of 1E-06 <br /> was used as a point of departure, and an excess cancer risk equal to or below this threshold was <br /> ' considered to be insignificant. If the excess cancer risk is within the acceptable range between <br /> 1E-04 and 1E-06, DTSC will make risk management decisions on a site-specific basis. For non- <br /> carcinogenic hazard indices, a hazard index of 1 or less is considered to be an acceptable health <br /> ' hazard level. If the regulatory criteria are exceeded based on the screening evaluation, this <br /> evaluation identifies the chemical and the exposure pathways contributing to the elevated risks or <br /> hazards, which can be more precisely assessed in a site-specific refined health risk assessment, if <br /> ' warranted. <br /> 5.1 RESIDENTIAL CANCER RISKS <br /> For potential on-site residential receptors, the oral and dermal cancer risks and inhalation cancer <br /> risks for exposure to on-site soils were calculated using the following equations: <br /> Oral and Dermal Cancer Risks for Direct Contact with Soil (PEA Guidance Manual, Figure 2.3): <br /> Risksoii = (SFo x Cs x [1.57E-06]) + (SFo x Cs x [1.87E-05] x ABS) <br /> Where: <br /> Risksoit = oral and dermal cancer risks from direct soil exposure <br /> SFo =oral cancer slope factor, (mg/kg-day)-1 <br /> Cs = concentration in soil, mg/kg <br /> ABS = dermal absorption fraction, dimensionless <br /> ' Table 8 shows the oral and dermal cancer risk calculations for potential residential exposures to <br /> soil at the site. Potential cancer risks were estimated for BTEX, PAHs, and metals, and then <br /> summed among chemicals for oral and dermal exposures. <br /> Inhalation Cancer Risks for Air (PEA Guidance Manual, Figure 2.4): <br /> Riskeir = SFi x Ca x 0.1.49 <br /> Where: <br /> 7 '-__ <br /> MENOMW`® <br /> From Science!o Solutions <br />