40 C.F.R. § 797.1330
(b)
Definitions. The definitions in section 3 of the Toxic Substances Control Act (TSCA), and the definitions in
part 792 Good Laboratory Practice Standards of this chapter apply to this test guideline. In addition, the following definitions apply to this guideline:
(1)
Brood stock means the animals which are cultured to produce test organisms through reproduction.
(2)
Chronic toxicity test means a method used to determine the concentration of a substance in water that produces an adverse effect on a test organism over an extended period of time. In this test guideline, mortality and reproduction (and optionally, growth) are the criteria of toxicity.
(3)
EC— 50 means that experimentally derived concentration of test substance in dilution water that is calculated to affect 50 percent of a test population during continuous exposure over a specified period of time. In this guideline, the effect measured is immobilization.
(4)
Ephippium means a resting egg which develops under the carapace in response to stress conditions in daphnids.
(5)
Flow-through means a continuous or intermittent passage of test solution or dilution water through a test chamber or culture tank with no recycling.
(6)
Immobilization means the lack of movement by daphnids except for minor activity of the appendages.
(7)
Loading means the ratio of daphnid biomass (grams, wet weight) to the volume (liters) of test solution in a test chamber at a point in time or passing through the test chamber during a specific interval.
(8)
MATC (Maximum Acceptable Toxicant Concentration) means the maximum concentration at which a chemical can be present and not be toxic to the test organism.
(9)
Renewal system means the technique in which test organisms are periodically transferred to fresh test solution of the same composition.
(e)
Reporting. The sponsor shall submit to the U.S. Environmental Protection Agency all data developed by the test that are suggestive or predictive of chronic toxicity and all associated toxicologic manifestations. In addition to the reporting requirements prescribed in the
part 792—Good Laboratory Practice Standards of this chapter the reporting of test data shall include the following:
(1)
The name of the test, sponsor, testing laboratory, study director, principal investigator, and dates of testing.
(2)
A detailed description of the test substance including its source, lot number, composition (identity and concentration of major ingredients and major impurities), known physical and chemical properties, and any carriers or other additives used and their concentrations.
(3)
The source of the dilution water, its chemical characteristics (e.g., conductivity, hardness, pH), and a description of any pretreatment.
(4)
Detailed information about the daphnids used as brood stock, including the scientific name and method of verification, age, source, treatments, feeding history, acclimation procedures, and culture methods. The age of the daphnids used in the test shall be reported.
(5)
A description of the test chambers, the volume of solution in the chambers, the way the test was begun (e.g., conditioning, test substance additions), the number of test organisms per test chamber, the number of replicates per treatment, the lighting, the renewal process and schedule for the renewal chronic test, the test substance delivery system and flow rate expressed as volume additions per 24 hours for the flow-through chronic test, and the method of feeding (manual or continuous) and type of food.
(6)
The concentration of the test substance in test chambers at times designated for renewal and flow-through tests.
(7)
The number and percentage of organisms that show any adverse effect in each test chamber at each observation period.
(8)
The cumulative adult and offspring immobilization values and the progeny produced at designated observation times, the time (days) to first brood and the number of offspring per adult in the control replicates and in each treatment replicate.
(9)
All chemical analyses of water quality and test substance concentrations, including methods, method validations and reagent blanks.
(10)
The data records of the culture, acclimation, and test temperatures.
(11)
Any deviation from this test guideline, and anything unusual about the test, (e.g., dilution failure, temperature fluctuations).
(12)
The MATC to be reported is calculated as the geometric mean between the lowest measured test substance concentration that had a significant (p≤0.05) effect and the highest measured test substance concentration that had no significant (p≤0.05) effect on day 21 of the test. The most sensitive of the test criteria (number of adult animals immobilized, the number of young per female and the number of immobilized young per female) is used to calculate the MATC. The criterion selected for MATC computation is the one which exhibits an effect (a statistically significant difference between treatment and control groups; p≤0.05) at the lowest test substance concentration for the shortest period of exposure. Appropriate statistical tests (analysis of variance, mean separation test) shall be used to test for significant test substance effects. The statistical tests employed and the results of these tests shall be reported.
(13)
Concentration-response curves utilizing the average measured test substance concentration shall be fitted to cumulative adult immobilization data at 21 days. A statistical test of goodness-of-fit shall be performed and the results reported.
(14)
An EC50 value based on adult immobilization with corresponding 95 percent confidence limits when sufficient data are present for day 21. These calculations shall be made using the average measured concentration of the test substance.
Notes, amendments, and revision history
Amendments
[50 FR 39321, Sept. 27, 1985, as amended at 52 FR 19060, May 20, 1987]
Authority
Authority: 15 U.S.C. 2603.
Source
Source: 50 FR 39321, Sept. 27, 1985, unless otherwise noted.
Amendments
[50 FR 39321, Sept. 27, 1985, as amended at 52 FR 19060, May 20, 1987]