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Interlaboratory Comparison of Three Sediment Bioaccumulation Tests

Standard bioaccumulation tests are commonly conducted using Macoma nasuta (clam), and Alitta virens (polychaete) for marine tests, and Lumbriculus variegatus (an oligochaete) for freshwater tests. Because the interlaboratory variability associated with these tests is unknown, four experienced labora...

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Autores principales: Lotufo, Guilherme R., Biedenbach, James M., Farrar, J. Daniel, Chanov, Michael K., Hester, Brian W., Warbritton, C. Ryan, Steevens, Jeffery A., Netchaev, Jenifer M., Bednar, Anthony J., Moore, David W.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310598/
https://www.ncbi.nlm.nih.gov/pubmed/35349191
http://dx.doi.org/10.1002/etc.5300
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author Lotufo, Guilherme R.
Biedenbach, James M.
Farrar, J. Daniel
Chanov, Michael K.
Hester, Brian W.
Warbritton, C. Ryan
Steevens, Jeffery A.
Netchaev, Jenifer M.
Bednar, Anthony J.
Moore, David W.
author_facet Lotufo, Guilherme R.
Biedenbach, James M.
Farrar, J. Daniel
Chanov, Michael K.
Hester, Brian W.
Warbritton, C. Ryan
Steevens, Jeffery A.
Netchaev, Jenifer M.
Bednar, Anthony J.
Moore, David W.
author_sort Lotufo, Guilherme R.
collection PubMed
description Standard bioaccumulation tests are commonly conducted using Macoma nasuta (clam), and Alitta virens (polychaete) for marine tests, and Lumbriculus variegatus (an oligochaete) for freshwater tests. Because the interlaboratory variability associated with these tests is unknown, four experienced laboratories conducted standard 28‐day bioaccumulation tests with the above species using sediments contaminated with polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs). Chemical analysis of tissue samples was performed by a single laboratory. The intralaboratory variance among replicates was relatively low for PCB tissue concentrations, with coefficients of variation (CVs) ranging from 9% to 28% for all laboratories and species, with the exception of one laboratory reporting higher variability for L. variegatus (CV = 51%). Intralaboratory variance for PCB tissue concentrations was higher than interlaboratory variance for A. virens and L. variegatus, and the magnitude of difference (MOD) for laboratory means ranged from 1.4 to 2.0 across species. Intralaboratory variability was also low for lipid content, and lipid normalization of PCB and PAH body residues generally had little impact on variability. In addition to variability across bioassay laboratories, analytical variability was evaluated by different laboratories measuring the concentration of PCBs and total lipids in a subsample of tissue homogenate of sediment‐exposed test organisms. Variability associated with tissue analysis was higher than bioassay laboratory variability only in tests with L. variegatus. Statistical differences between samples may be observed due to the low intralaboratory variability; however, the biological significance of these differences may be limited because the MOD is low. Considering the MOD when comparing bioaccumulation across treatments accounts for uncertainty related to inherent variability of the test in the interpretation of statistically significant results. Environ Toxicol Chem 2022;41:1260–1275. © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC. This article has been contributed to by US Government employees and their work is in the public domain in the USA.
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spelling pubmed-93105982022-07-29 Interlaboratory Comparison of Three Sediment Bioaccumulation Tests Lotufo, Guilherme R. Biedenbach, James M. Farrar, J. Daniel Chanov, Michael K. Hester, Brian W. Warbritton, C. Ryan Steevens, Jeffery A. Netchaev, Jenifer M. Bednar, Anthony J. Moore, David W. Environ Toxicol Chem Environmental Toxicology Standard bioaccumulation tests are commonly conducted using Macoma nasuta (clam), and Alitta virens (polychaete) for marine tests, and Lumbriculus variegatus (an oligochaete) for freshwater tests. Because the interlaboratory variability associated with these tests is unknown, four experienced laboratories conducted standard 28‐day bioaccumulation tests with the above species using sediments contaminated with polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs). Chemical analysis of tissue samples was performed by a single laboratory. The intralaboratory variance among replicates was relatively low for PCB tissue concentrations, with coefficients of variation (CVs) ranging from 9% to 28% for all laboratories and species, with the exception of one laboratory reporting higher variability for L. variegatus (CV = 51%). Intralaboratory variance for PCB tissue concentrations was higher than interlaboratory variance for A. virens and L. variegatus, and the magnitude of difference (MOD) for laboratory means ranged from 1.4 to 2.0 across species. Intralaboratory variability was also low for lipid content, and lipid normalization of PCB and PAH body residues generally had little impact on variability. In addition to variability across bioassay laboratories, analytical variability was evaluated by different laboratories measuring the concentration of PCBs and total lipids in a subsample of tissue homogenate of sediment‐exposed test organisms. Variability associated with tissue analysis was higher than bioassay laboratory variability only in tests with L. variegatus. Statistical differences between samples may be observed due to the low intralaboratory variability; however, the biological significance of these differences may be limited because the MOD is low. Considering the MOD when comparing bioaccumulation across treatments accounts for uncertainty related to inherent variability of the test in the interpretation of statistically significant results. Environ Toxicol Chem 2022;41:1260–1275. © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC. This article has been contributed to by US Government employees and their work is in the public domain in the USA. John Wiley and Sons Inc. 2022-03-29 2022-05 /pmc/articles/PMC9310598/ /pubmed/35349191 http://dx.doi.org/10.1002/etc.5300 Text en © 2022 The Authors. Environmental Toxicology and Chemistry published by Wiley Periodicals LLC on behalf of SETAC. This article has been contributed to by US Government employees and their work is in the public domain in the USA https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ (https://creativecommons.org/licenses/by-nc-nd/4.0/) License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Environmental Toxicology
Lotufo, Guilherme R.
Biedenbach, James M.
Farrar, J. Daniel
Chanov, Michael K.
Hester, Brian W.
Warbritton, C. Ryan
Steevens, Jeffery A.
Netchaev, Jenifer M.
Bednar, Anthony J.
Moore, David W.
Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title_full Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title_fullStr Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title_full_unstemmed Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title_short Interlaboratory Comparison of Three Sediment Bioaccumulation Tests
title_sort interlaboratory comparison of three sediment bioaccumulation tests
topic Environmental Toxicology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9310598/
https://www.ncbi.nlm.nih.gov/pubmed/35349191
http://dx.doi.org/10.1002/etc.5300
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