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Homepage>ASTM Standards>07>07.080>ASTM E1022-22 - Standard Guide for Conducting Bioconcentration Tests with Fishes and Saltwater Bivalve Mollusks
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Released: 01.04.2022

ASTM E1022-22 - Standard Guide for Conducting Bioconcentration Tests with Fishes and Saltwater Bivalve Mollusks

Standard Guide for Conducting Bioconcentration Tests with Fishes and Saltwater Bivalve Mollusks

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Standard number:ASTM E1022-22
Released:01.04.2022
Status:Active
Pages:19
Section:11.06
Keywords:bioaccumulation; bioconcentration; bioconcentration factor (BCF); bivalve mollusks; depuration phase; fishes; uptake phase ;
DESCRIPTION

1.1 This guide describes procedures for obtaining laboratory data concerning bioconcentration of a test material added to dilution water—but not to food—by freshwater and saltwater fishes and saltwater bivalve mollusks using the flow-through technique. These procedures also should be useful for conducting bioconcentration tests with other aquatic species, although modifications might be necessary.

1.2 Other modifications of these procedures might be justified by special needs or circumstances. Although using appropriate procedures is more important than following prescribed procedures, the results of tests conducted using unusual procedures are not likely to be comparable to those of many other tests. The comparison of results obtained using modified and unmodified versions of these procedures might provide useful information concerning new concepts and procedures for conducting bioconcentration tests.

1.3 These procedures are applicable to all chemicals that can be measured accurately at the necessary concentrations in water and in appropriate tissues. Bioconcentration tests are usually conducted on individual chemicals but can be conducted on mixtures if appropriate measurements can be made. Some techniques described in this guide were developed for tests on non-ionizable organic chemicals (see 11.1.2.1) and might not apply to ionizable or inorganic chemicals.

1.4 Results of bioconcentration tests should usually be reported in terms of apparent steady-state and projected steady-state bioconcentration factors (BCFs) and uptake and depuration rate constants. Results should be reported in terms of whole body for fishes and in terms of total soft tissue for bivalve mollusks. For fishes and scallops consumed by humans, some results should also be reported in terms of the edible portion, especially if ingestion of the test material by humans is a major concern. For tests on organic and organometallic chemicals, the percent lipids of the tissue should be reported.

1.5 This guide is arranged as follows:

 

Section

Referenced Documents

2

Terminology

3

Summary of Guide

4

Significance and Use

5

Safety Precautions

7

Apparatus

6

 Facilities

6.1

 Construction Materials

6.2

 Metering System

6.3

 Test Chambers

6.4

 Cleaning

6.4.4

 Acceptability

6.5

Dilution Water

8

 Requirements

8.1

 Source

8.2

 Treatment

8.3

 Characterization

8.4

Test Material

9

 General

9.1

 Radiolabeled Material

9.2

 Stock Solution

9.3

 Test Concentration(s)

9.4

Test Organisms

10

 Species

10.1

 Size

10.2

 Source

10.3

 Care and Handling

10.4

 Feeding

10.5

 Disease Treatment

10.6

 Holding

10.7

 Acclimation

10.8

 Quality

10.9

Procedure

11

 Experimental Design

11.1

 Dissolved Oxygen

11.2

 Temperature

11.3

 Loading

11.4

 Beginning the Test

11.5

 Care of Organisms

11.6

 Feeding

11.7

 Cleaning

11.8

 Biological Data

11.9

 Measurements on Test Solutions

11.10

Analytical Methodology

12

Acceptability of Test

13

Calculation of Results

14

Documentation

15

Keywords

16

1.6 The values stated in SI units are to be regarded as standard. No other units of measurement are included in this standard.

1.7 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety, health, and environmental practices and determine the applicability of regulatory limitations prior to use.Specific precautionary statements are given in Section 7.

This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

1.8 This international standard was developed in accordance with internationally recognized principles on standardization established in the Decision on Principles for the Development of International Standards, Guides and Recommendations issued by the World Trade Organization Technical Barriers to Trade (TBT) Committee.