1. THE DECLARATION


  1. Site Name and Location
  2. Statement of Basis and Purpose
  3. Assessment of Site
  4. Description of the Selected Remedy
  5. Statutory Determinations

1.1. Site Name and Location

The Lawrence Livermore National Laboratory (LLNL) Livermore site, located at 7000 East Avenue, Livermore, California, is a research and development facility owned by the U.S. Department of Energy (DOE) and operated by the University of California. LLNL was placed on the U.S. Environmental Protection Agency's (EPA) National Priorities List (NPL) in 1987. Currently, about 10,000 people use ground water blended from several downtown Livermore municipal supply wells as their primary drinking water supply. Contaminants from LLNL are currently about 1.6 miles from these supply wells. U.S. EPA, in conjunction with the California Department of Toxic Substances Control (DTSC) and the California Regional Water Quality Control Board (RWQCB), oversees LLNL's investigations and cleanup activities in accordance with Section 120 of the Comprehensive Environmental Response, Compensation, and Liability Act of 1980 (CERCLA), as amended.


1.2. Statement of Basis and Purpose

This decision document presents the selected remedial actions for the LLNL Livermore site, in Livermore, California, which were chosen in accordance with CERCLA, as amended by the Superfund Amendments and Reauthorization Act of 1986 (SARA), and, to the extent practicable, the National Oil and Hazardous Substances Pollution Contingency Plan (NCP). This decision document is based on the administrative record for this site.

The U.S. EPA, the RWQCB, and the DTSC of the California Environmental Protection Agency, formerly the California Department of Health Services (DHS), concur with the selected remedies.


1.3. Assessment of Site

The identified compounds of concern, if not addressed by the selected remedies or other considered measures, may present a potential risk to public health as discussed in the Proposed Remedial Action Plan (PRAP) for the site.


1.4. Description of the Selected Remedy

The Feasibility Study (FS) evaluated many potential remedies for the LLNL site. Those remedies were divided into two general groups, according to whether the chemical contaminants are in ground water or in unsaturated sediment (i.e., sediment above the water table where pore spaces are only partially filled with water). Three alternatives were evaluated for the ground water plume, and two remedies were evaluated for the unsaturated zone (i.e., the interval above the water table where pore spaces are only partially filled with water).

The selected remedy for ground water is Remedial Alternative No. 1 from the FS, which includes:

The selected remedy for treating the unsaturated zone is Remedial Alternative No. 1 from the FS. This alternative includes using a process called vacuum-induced venting to extract the contaminants in vapor form from the unsaturated sediments, and treating the vapors by catalytic oxidation and activated carbon.

The selected remedies address the principal concerns at the LLNL site by removing contaminants in ground water and soil vapor and treating them at the surface to levels protective of human health and the environment.

This Record of Decision (ROD) applies to all known contaminants in ground water and unsaturated sediment originating from activities at the LLNL site. An additional potential source of hazardous materials (i.e., the Trailer 5475/East Taxi Strip Area) was identified after completion of the PRAP on the LLNL site. If future investigations identify additional public health or environmental risks from this or other potential sources, this ROD may be augmented through CERCLA/SARA and the NCP to address any additional action.


1.5. Statutory Determinations

The selected remedies are protective of human health and the environment, comply with Federal and State requirements that are legally applicable or relevant and appropriate to the remedial action, and are cost-effective. The remedies utilize permanent solutions and alternative treatment technology, to the maximum extent practicable, and satisfy the statutory preference for remedies that employ treatment that reduces toxicity, mobility, or volume as a principal element. Because these remedies may result in hazardous materials remaining onsite above health-based levels until cleanup is complete, a review will be conducted within 5 years after commencement of remediation to assure that the remedies continue to provide adequate protection of human health and the environment.



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October 1, 2007

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