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Page Title: USEPA Environmental Response Team (Cont.)
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This document describes, with examples, eight steps for doing an ecological risk
assessment. Steps 1 and 2 of the EPA guidance are designed to allow risk
assessors and risk managers to quickly determine whether a site poses a risk to the
environment.
Step 1 - Screening-level problem formulation and ecological effects evaluation
In the problem formulation component of Step 1, all parties involved in the
risk assessment, including site managers, risk assessors, the Biological Technical
Assistance Group (BTAG), the Potentially Responsible Party (PRP), and
stakeholders, work together to define the goals of the assessment and to propose a
scope for remedial action. This problem formulation step is critical to focus the
scope of work for the risk assessment. Step 1 also includes a toxicity evaluation to
determine what specific component of the ecosystem could be adversely affected
by contaminants from the site (ecological effects evaluation).
Step 2 - Screening-level estimate and risk calculation
The goal of this step is to decide whether a significant ecological risk has been
identified, based on screening assessment results, or if a more detailed risk
assessment should be conducted. At the end of Step 2 is a scientific/management
decision point (SMDP). SMDPs occur at defined points in the assessment process.
The purpose of SMDPs is to guide work, discuss the uncertainty of risk
assessment, and to keep lines of communication open between parties working on
the assessment. In this way, SMDPs ensure that time and money are not wasted
due to flawed decisions, miscommunication, or misunderstandings while
conducting the risk assessment.
Step 3 - Baseline risk assessment and problem formulation
If the results of the screening-level assessment from Steps 1 and 2 prove
insufficient to rule out risk to the environment or if they indicate that some
significant risk is present, then the assessment proceeds to Step 3. This step uses
the screening assessment results in conjunction with more site-specific
information to refine the problem formulation and expand on ecological issues of
concern. Specifically, assessment endpoints, exposure pathways, and risk
questions are developed. Step 3 also involves the development of a site conceptual
model, which integrates the above three components. The purpose of the SMDP at
the end of Step 3 is to determine if this conceptual model is acceptable.
Step 4 - Study design and data quality objective process
Step 4 uses the conceptual model developed in Step 3 to define measurement
endpoints, data quality objectives (DQOs), and the study design. These
components are directly integrated into the products of Step 4, an ecological risk
assessment work plan (WP) and a sampling and analysis plan (SAP). The WP and
SAP are critical to be able to gather enough information for the risk assessor to
A10
Appendix A Summary of Federal, State, and Regional Guidance

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