{"title":"微泡臭氧氧化降低铜绿微囊藻的毒性","authors":"Gwiwoong Nam, M. Jeon, Yoon-E Choi, Jinho Jung","doi":"10.1080/01919512.2022.2052013","DOIUrl":null,"url":null,"abstract":"ABSTRACT The aim of this study was to investigate microbubble ozonation for the removal of toxic cyanobacteria, Microcystis aeruginosa. The microbubble ozonation (30 min) at 3.47 mg O3 L−1 decreased the M. aeruginosa concentration from 1.5 × 107 to 0.8 × 107 cell mL−1. However, the acute toxicity (48 h) to Daphnia magna (<24 h old) was considerably increased after the microbubble ozonation, possibly owing to the release of intracellular microcystins (MCs). Considering the release of toxic MCs, the microbubble ozonation was optimized at an environmentally relevant concentration (1.74 × 106 cell mL−1) of M. aeruginosa. Microbubble ozonation at 0.26–1.92 mg O3 L−1 for 30 min removed M. aeruginosa by 26 to 83% without any acute toxicity on D. magna. Moreover, D. magna feeding enhanced the removal rate from 85 to 100% for 48 h. These findings suggest that microbubble ozonation, possibly combined with D. magna biomanipulation, can be a promising tool to control toxic cyanobacteria in ambient water.","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2022-03-13","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"2","resultStr":"{\"title\":\"Toxicity Reduction of Microcystis Aeruginosa Using Microbubble Ozonation\",\"authors\":\"Gwiwoong Nam, M. Jeon, Yoon-E Choi, Jinho Jung\",\"doi\":\"10.1080/01919512.2022.2052013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"ABSTRACT The aim of this study was to investigate microbubble ozonation for the removal of toxic cyanobacteria, Microcystis aeruginosa. The microbubble ozonation (30 min) at 3.47 mg O3 L−1 decreased the M. aeruginosa concentration from 1.5 × 107 to 0.8 × 107 cell mL−1. However, the acute toxicity (48 h) to Daphnia magna (<24 h old) was considerably increased after the microbubble ozonation, possibly owing to the release of intracellular microcystins (MCs). Considering the release of toxic MCs, the microbubble ozonation was optimized at an environmentally relevant concentration (1.74 × 106 cell mL−1) of M. aeruginosa. Microbubble ozonation at 0.26–1.92 mg O3 L−1 for 30 min removed M. aeruginosa by 26 to 83% without any acute toxicity on D. magna. Moreover, D. magna feeding enhanced the removal rate from 85 to 100% for 48 h. These findings suggest that microbubble ozonation, possibly combined with D. magna biomanipulation, can be a promising tool to control toxic cyanobacteria in ambient water.\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2022-03-13\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"2\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"93\",\"ListUrlMain\":\"https://doi.org/10.1080/01919512.2022.2052013\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"93","ListUrlMain":"https://doi.org/10.1080/01919512.2022.2052013","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
Toxicity Reduction of Microcystis Aeruginosa Using Microbubble Ozonation
ABSTRACT The aim of this study was to investigate microbubble ozonation for the removal of toxic cyanobacteria, Microcystis aeruginosa. The microbubble ozonation (30 min) at 3.47 mg O3 L−1 decreased the M. aeruginosa concentration from 1.5 × 107 to 0.8 × 107 cell mL−1. However, the acute toxicity (48 h) to Daphnia magna (<24 h old) was considerably increased after the microbubble ozonation, possibly owing to the release of intracellular microcystins (MCs). Considering the release of toxic MCs, the microbubble ozonation was optimized at an environmentally relevant concentration (1.74 × 106 cell mL−1) of M. aeruginosa. Microbubble ozonation at 0.26–1.92 mg O3 L−1 for 30 min removed M. aeruginosa by 26 to 83% without any acute toxicity on D. magna. Moreover, D. magna feeding enhanced the removal rate from 85 to 100% for 48 h. These findings suggest that microbubble ozonation, possibly combined with D. magna biomanipulation, can be a promising tool to control toxic cyanobacteria in ambient water.