An official website of the United States government.

We've made some changes to EPA.gov. If the information you are looking for is not here, you may be able to find it on the EPA Web Archive or the January 19, 2017 Web Snapshot.

EPA EcoBox

EPA EcoBox Tools by Effects - Effects In ERA

Planning and Problem Formulation Phase: Identifying Potential Ecological Effects

According to U.S. EPA’s Guidelines for Ecological Risk Assessment (1998), problem formulation is a process for generating and evaluating preliminary hypotheses about why ecological effects have occurred—or may occur—from human activities. The process of problem formulation offers a systematic approach for organizing and evaluating available information on stressorsHelpstressorsAny physical, chemical, or biological entity that can induce an adverse response (synonymous with agent). and possible effects. During this process, the following questions related to ecological effects might be considered.

  • What are the type and extent of available ecological effects information (e.g., field surveys, laboratory tests, or structure-activity relationships)?
  • Given the nature of the stressor(s) (if known), which effects are expected to be elicited by the stressor(s)?
  • Under what circumstances will effects occur?

A plan for analyzing and characterizing ecological risks is determined based on the integration of available information on sources, stressors, effects, and ecosystem and receptor characteristics.

Analysis Phase: Characterizing Effects

During the analysis phase—which comprises exposure assessment and effects assessment—ecological effects are characterized. As described in U.S. EPA’s Guidelines for Ecological Risk Assessment (1998), to characterize ecological effects associated with a stressor, assessors do the following:

Top of Page

For narrowly defined assessments of a single stressor and effect, the calculated relationship may be expressed as a stressor-response curveHelpstressor-response curveA graphic, quantitative representation of the relationship between a stressor and an ecological effect. or summarized as a single reference value (a point on the curve [e.g., LD50]). In many cases, however, more complex interrelationships are present. Effect levels can be expressed in terms of lethality (e.g., LC50 or LD50) or effects other than lethality like growth and reproduction (e.g., EC50 or ED50). In conducting a toxicity test, an assessor might choose to establish no-effect stressor level (e.g., NOAEL) or lowest-effect stressor level (e.g., LOAEL) based on comparisons between experimental treatments and controls.

Top of Page

Below is a simple example of a stressor-response curve that shows a range of responses for increasing stressor intensity. The points represent lethal dose (LD) levels for a given percent of the population. The shape of the stressor-response curve may be needed to determine the presence or absence of thresholdsHelpthresholdsA concentration above which some effect (or response) will be produced and below which it will not. for significant effects or to evaluate incremental risks (U.S. EPA, 1998). The lower bound of a threshold would be based on consistent conservative assumptions and NOAEL toxicity values. The upper bound would be based on observed impacts or predictions that ecological impacts could occur. This upper bound would be developed using consistent assumptions, site-specific data, LOAEL toxicity values, or an impact evaluation (U.S. EPA, 1997; 1996).

Increase Intensity of Stressor

EPA estimates the toxicity or hazard of a stressor by evaluating ecological effects tests that vary from short-term (acute) to long-term (chronic) laboratory studies and might also include field studies. In these tests, animals and plants are exposed to different amounts of a stressor, and their responses to these varying concentrations are measured. The results of these tests may be used to establish a dose-response or cause-and-effect relationship between the amount of stressor to which the organism is exposed and the effects on the organism.

Some of the impacts or ecological effects that are measured in ecotoxicity tests include:

  • mortality,
  • reduction in growth,
  • reproductive impairment,
  • changes in numbers of species,
  • bioaccumulation of residues in non-target organisms, and
  • disruption of community and ecosystem-level functions.

The table below provides examples of toxicity endpoints that might be used in a screening assessment to calculate risk for aquatic and terrestrial receptors.

Assessment Type Example Endpoint Ecological Effects Test Guidelines1
Aquatic
Acute aquatic assessment Lowest tested EC50 or LC50 for freshwater fish and invertebrates and estuarine/marine fish and invertebrates from acute toxicity tests. OCSPP 850.1010
Aquatic Invertebrate Acute Toxicity Test, Freshwater Daphnids

OCSPP 850.1075
Freshwater and Saltwater Fish Acute Toxicity
Chronic aquatic assessment Lowest NOAEL for freshwater fish and invertebrates and estuarine/marine fish and invertebrates from early life-stage or full life-cycle tests. OCSPP 850.1300
Daphnid Chronic Toxicity Test

OCSPP 850.1400
Fish Early Life Stage Toxicity Test
Aquatic vascular plant and algae Lowest EC50 for vascular and algae. OCSPP 850.4400
Aquatic Plant Toxicity Test Using Lemna spp.

OCSPP 850.4500
Algal Toxicity
Terrestrial
Acute avian assessment Lowest LD50 (single oral dose) and LC50 (subacute dietary). OCSPP 850.2100
Avian Acute Oral Toxicity Test

OCSPP 850.2200
Avian Dietary Toxicity Test
Chronic avian assessment Lowest NOAEL for 21-week avian reproduction test. OCSPP 850.2300
Avian Reproduction Test
Acute mammalian assessment Lowest LD50 from single oral dose test. OCSPP 850.2400
Wild Mammal Toxicity Testing
Chronic mammalian assessment Lowest NOAEL for two-generation reproduction test. OCSPP 850.2400
Wild Mammal Toxicity Testing
Terrestrial non-endangered plant Lowest EC25 values from both seedling emergence and vegetative vigor for monocots and dicots. OCSPP 850.4150
Vegetative Vigor
Terrestrial endangered plant Lowest EC5 or NOAEL for both seedling emergence and vegetative vigor for monocots and dicots. OCSPP 850.4150
Vegetative Vigor

1Ecological Effects Test Guidelines (Series 850) are available at Series 850 - Ecological Effects Test Guidelines.

Literature reviews, laboratory toxicity tests, and field studies are measure-of-effect tools to help link contaminant concentrations to effects on ecological receptors (see table). These tools provide “dose-response” information: that is, how much toxicant is associated with how much of an adverse effect (U.S. EPA, 1991). Adverse ecological effects are changes that are considered undesirable because they alter valued structural or functional characteristics of ecosystems or their components. An evaluation of adversity may consider the type, intensity, and scale of the effect as well as the potential for recovery (U.S. EPA, 1998).

Measure of Effect Considerations
Literature reviews Literature reviews can provide specific dose-response information for a particular receptor. By comparing measured concentrations of contaminants in site media with literature values for adverse effects, investigators can decide whether they need to proceed with site-specific field studies or toxicity tests (U.S. EPA, 1991).
Laboratory toxicity tests

Toxicity tests evaluate the effects of stressors on the survival, growth, reproduction, and metabolism of test species. In reviewing test results along with data on stressor levels and biological observations from field studies, ecologists might find evidence that observed or predicted effects are attributable to the presence of the stressor. Toxicity tests could be used to demonstrate spatial extent of contamination and identify areas of high contaminant concentrations (U.S. EPA, 1991; 1994a; 1994b).

Because conditions can be controlled in laboratory studies, responses may be less variable and smaller differences easier to detect. However, the controls may limit the range of responses (e.g., animals cannot seek alternative food sources), so they may not reflect responses in the environment. In addition, there are multiple stressors in natural systems and larger-scale processes are difficult to replicate in the laboratory. Frequently, risk assessors extrapolate from laboratory toxicity test data to field effects (U.S. EPA, 1998).

Ecological field studies

Ecological field studies (surveys) offer direct or corroborative evidence of a link between a stressor and ecological effects. Evidence could include: reduction in population sizes of species, absence of species normally occurring in the habitat, presence of species associated primarily with stressed habitats, changes in community diversity or trophic structure, and incidence of lesions, tumors, or other pathologies. Ecologists might compare data on observed adverse effects to information obtained from a reference area not affected by the stressor (U.S. EPA, 1991; 1994c).

Field studies measure biological changes in uncontrolled situations. Field surveys usually represent exposures and effects (including secondary effects) better than estimates generated from laboratory studies or theoretical models. Field data are more important for assessments of multiple stressors or where site-specific factors significantly influence exposure. They are also often useful for analyses of larger geographic scales and higher levels of biological organization. Risks to organisms in field situations are best estimated from studies at the site of interest. However, such data are not always available. Field surveys are most useful for linking stressors with effects when stressor and effect levels are measured concurrently. The presence of confounding factors can make it difficult to attribute observed effects to specific stressors (U.S. EPA, 1998).

Top of Page

Risk Characterization: Quantifying Effects in Ecological Risks

The risk characterization quantifies the links between exposure to stressorsHelpstressorsAny physical, chemical, or biological entity that can induce an adverse response (synonymous with agent). and effects to ecological receptors and characterizes the types, extent, and severity of those risks. Completing risk characterization allows risk assessors to reach conclusions regarding the occurrence of exposure and the adversity of existing or anticipated effects (U.S. EPA, 1998).

During risk characterization, exposure and stressor-response profilesHelpstressor-response profilesThe product of characterization of ecological effects in the analysis phase of ecological risk assessment. The stressor-response profile summarizes the data on the effects of a stressor and the relationship of the data to the assessment endpoint. are integrated through the risk estimation process. The final product is a risk description in which the results of the integration are presented, including an interpretation of ecological adversity and descriptions of uncertainty and lines of evidence. The acceptability of adverse effects is determined by risk managers. In characterizing adversity, primary (direct) and secondary (indirect) effects are considered, and sometimes the impact of the secondary effects can outweigh that of the primary effect (U.S. EPA, 1998).

A common approach to quantifying ecological risks to receptors is to compare exposure concentrations of a stressor in an environmental medium by a toxicity reference value (TRV)—a concentration which if exceeded is expected to result in adverse ecological effects. Where exposure-response functions are not available or developed, the quotient method of comparing an estimated exposure concentration to a threshold for response can be used (U.S. EPA, 1997). Typically, the ratio (or quotient) is expressed as an exposure concentration divided by an effects concentration. Quotients are commonly used for chemical stressors for which reference or benchmark toxicity values are widely available (U.S. EPA, 1998).

References

Top of Page

Resources that provide information related to effects in ecological risk assessments are provided below.

Some content on this page requires JavaScript in order to be viewed. If you wish to view content on this page, you must have JavaScript enabled.

Top of Page