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Derivation of algal acute to chronic ratios for use in chemical toxicity extrapolations.
Brill, Jessica L; Belanger, Scott E; Barron, Mace G; Beasley, Amy; Connors, Kristin A; Embry, Michelle; Carr, Greg J.
Afiliação
  • Brill JL; The Procter and Gamble Company, 8700 Mason Montgomery Rd. Cincinnati, Ohio, 45040, USA. Electronic address: brill.jl@pg.com.
  • Belanger SE; The Procter and Gamble Company, 8700 Mason Montgomery Rd. Cincinnati, Ohio, 45040, USA. Electronic address: belanger.se@pg.com.
  • Barron MG; United States Environmental Protection Agency, 1 Sabine Dr. Gulf Breeze, FL, 32561, USA. Electronic address: Barron.Mace@epa.gov.
  • Beasley A; The Dow Chemical Company, 2030 Dow Center Employee Ctr. Midland, MI, 48674, USA. Electronic address: ABeasley@dow.com.
  • Connors KA; The Procter and Gamble Company, 8700 Mason Montgomery Rd. Cincinnati, Ohio, 45040, USA. Electronic address: connors.ka@pg.com.
  • Embry M; Health and Environmental Sciences Institute, 1 Thomas Cir NW STE9, Washington, DC, 20005, USA. Electronic address: membry@hesiglobal.org.
  • Carr GJ; The Procter and Gamble Company, 8700 Mason Montgomery Rd. Cincinnati, Ohio, 45040, USA. Electronic address: carr.gj@pg.com.
Chemosphere ; 263: 127804, 2021 Jan.
Article em En | MEDLINE | ID: mdl-33297001
ABSTRACT
Algal toxicity studies are required by regulatory agencies for a variety of purposes including classification and labeling and environmental risk assessment of chemicals. Algae are also frequently the most sensitive taxonomic group tested. Acute to chronic ratios (ACRs) have been challenging to derive for algal species because of the complexities of the underlying experimental data including a lack of universally agreed upon algal inhibition endpoints; evolution of experimental designs over time and by different standardization authorities; and differing statistical approaches (e.g., regression versus hypothesis-based effect concentrations). Experimental data for developing globally accepted algal ACRs have been limited because of data availability, and in most regulatory frameworks an ACR of 10 is used regardless of species, chemical type or mode of action. Acute and chronic toxicity (inhibition) data on 17 algal species and 442 chemicals were compiled from the EnviroTox database (https//envirotoxdatabase.org/) and a proprietary database of algal toxicity records. Information was probed for growth rate, yield, and final cell density endpoints focusing primarily on studies of 72 and 96 h duration. Comparisons of acute and chronic data based on either single (e.g., growth rate) and multiple (e.g., growth rate, final cell density) endpoints were used to assess acute and chronic relationships. Linear regressions of various model permutations were used to compute ACRs for multiple combinations of taxa, chemicals, and endpoints, and showed that ACRs for algae were consistently around 4 (ranging from 2.43 to 5.62). An ACR of 4 for algal toxicity is proposed as an alternative to a default value of 10, and recommendations for consideration and additional research and development are provided.
Assuntos

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Químicos da Água Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: Chemosphere Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Poluentes Químicos da Água Tipo de estudo: Etiology_studies / Risk_factors_studies Idioma: En Revista: Chemosphere Ano de publicação: 2021 Tipo de documento: Article