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Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter
The freshwater flagellate alga Euglena agilis Carter was exposed to the polycyclic aromatic hydrocarbon (PAH) anthracene for 96 h under optimal photosynthetically active radiation (PAR), and responses of growth, photosynthetic pigment production, and photosynthetic efficiency were assessed. Anthrace...
Autores principales: | , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814832/ https://www.ncbi.nlm.nih.gov/pubmed/31653882 http://dx.doi.org/10.1038/s41598-019-51451-y |
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author | Kottuparambil, Sreejith Park, Jihae |
author_facet | Kottuparambil, Sreejith Park, Jihae |
author_sort | Kottuparambil, Sreejith |
collection | PubMed |
description | The freshwater flagellate alga Euglena agilis Carter was exposed to the polycyclic aromatic hydrocarbon (PAH) anthracene for 96 h under optimal photosynthetically active radiation (PAR), and responses of growth, photosynthetic pigment production, and photosynthetic efficiency were assessed. Anthracene reduced the growth rate (μ) and levels of chlorophyll a (Chl a), chlorophyll b (Chl b), and total carotenoids. The growth rate was more sensitive than photosynthetic parameters, with a median effective concentration (EC(50)) of 4.28 mg L(−1). Between 5 and 15 mg L(−1), anthracene inhibited the maximum quantum yield (F(v)/F(m)) of photosystem II (PSII) and the maximum photosynthetic electron transport rate through PSII (rETR(max)) with EC(50) values of 14.88 and 11.8 mg L(−1), respectively. At all anthracene concentrations, intracellular reactive oxygen species (ROS) were elevated, indicating increased oxidative stress. Anthracene presumably reduced the PSII efficiency of photochemical energy regulation and altered the photochemistry through intracellular ROS formation. Acute exposure to PAHs may induce severe physiological changes in phytoplankton cells, which may influence vital ecological processes within the aquatic environments. Additionally, growth and Chl a content may serve as sensitive risk assessment parameters of anthracene toxicity in water management since EC(50) values for both overlap with anthracene levels (8.3 mg L(−1)) permitted by the US Environmental Protection Agency (USEPA). |
format | Online Article Text |
id | pubmed-6814832 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-68148322019-10-30 Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter Kottuparambil, Sreejith Park, Jihae Sci Rep Article The freshwater flagellate alga Euglena agilis Carter was exposed to the polycyclic aromatic hydrocarbon (PAH) anthracene for 96 h under optimal photosynthetically active radiation (PAR), and responses of growth, photosynthetic pigment production, and photosynthetic efficiency were assessed. Anthracene reduced the growth rate (μ) and levels of chlorophyll a (Chl a), chlorophyll b (Chl b), and total carotenoids. The growth rate was more sensitive than photosynthetic parameters, with a median effective concentration (EC(50)) of 4.28 mg L(−1). Between 5 and 15 mg L(−1), anthracene inhibited the maximum quantum yield (F(v)/F(m)) of photosystem II (PSII) and the maximum photosynthetic electron transport rate through PSII (rETR(max)) with EC(50) values of 14.88 and 11.8 mg L(−1), respectively. At all anthracene concentrations, intracellular reactive oxygen species (ROS) were elevated, indicating increased oxidative stress. Anthracene presumably reduced the PSII efficiency of photochemical energy regulation and altered the photochemistry through intracellular ROS formation. Acute exposure to PAHs may induce severe physiological changes in phytoplankton cells, which may influence vital ecological processes within the aquatic environments. Additionally, growth and Chl a content may serve as sensitive risk assessment parameters of anthracene toxicity in water management since EC(50) values for both overlap with anthracene levels (8.3 mg L(−1)) permitted by the US Environmental Protection Agency (USEPA). Nature Publishing Group UK 2019-10-25 /pmc/articles/PMC6814832/ /pubmed/31653882 http://dx.doi.org/10.1038/s41598-019-51451-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Kottuparambil, Sreejith Park, Jihae Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title | Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title_full | Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title_fullStr | Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title_full_unstemmed | Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title_short | Anthracene phytotoxicity in the freshwater flagellate alga Euglena agilis Carter |
title_sort | anthracene phytotoxicity in the freshwater flagellate alga euglena agilis carter |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6814832/ https://www.ncbi.nlm.nih.gov/pubmed/31653882 http://dx.doi.org/10.1038/s41598-019-51451-y |
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