Journal of Water and Environment Technology
Online ISSN : 1348-2165
ISSN-L : 1348-2165
Original Articles
An Analytical Method for Simultaneous Measurement of Various Cyanotoxins Using Stable Isotope-Labeled Surrogates and a Microbial Flora Analysis to Assign Each Cyanotoxin to its Source
Masaya MatsukiNobuhiro ShimizuKazuhiro TobiishiYoshito TanakaHaruyo YamaguchiTomoharu Sano
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ジャーナル オープンアクセス

2022 年 20 巻 6 号 p. 261-272

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Cyanotoxins produced by blue-green algae in lakes are among the most serious threats to water quality worldwide. As global warming rapidly extends the locations and timing of blue-green algae blooms, a simple and accessible method for the detection and quantification of cyanotoxins in fresh water is increasingly necessary. Here, a quick, simple and accessible simultaneous analytical method for five cyanotoxins (cylindrospermopsin, anatoxin-a, microcystin-RR, YR and LR) is reported. This method has three advantages. First, it does not require complicated operations, such as a concentration operation. Second, it employs an HPLC column without high pressure. Third, the use of stable isotope-labeled surrogates enables correct identification and precise quantification of cyanotoxins. The method was applied to the lakes of Fukuoka Prefecture in Japan, and four of the five above-named cyanotoxins (i.e., all but cylindrospermopsin) were detected. The limits of quantification were 20–43 ng/L, which were considerably lower than the WHO guideline values. The recovery levels were 97–104%. Microbial flora analysis revealed that the sources of anatoxin-a were Pseudanabaena limnetica and Cuspidothrix issatschenkoi, and the source of microcystins was the group A1 of Microcystis aeruginosa. This study provides a quick, easy and accessible method for the worldwide monitoring of cyanotoxin levels.

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© 2022 Japan Society on Water Environment

This is an open-access article distributed under the terms of the Creative Commons Attribution Non-Commercial (CC BY-NC) 4.0 License.
https://creativecommons.org/licenses/by-nc/4.0/deed.ja
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