Comparison of different algicides on growth of Microcystis aeruginosa and microcystin release, as well as its removal pathway in riverways
Naiyu Wang, Kai Wang, Can Wang
Comparison of different algicides on growth of Microcystis aeruginosa and microcystin release, as well as its removal pathway in riverways
Aluminum silicate is the most effective algicide on Microcystis aeruginosa control.
Algicides increased MC-LR concentration by disrupting M. aeruginosa cells.
Acute biotoxicity and extracellular MC-LR concentration were positively correlated.
MC-LR was mainly removed by benthal sludge and UV-rays under natural conditions.
Eutrophication with a large number of Microcystis aeruginosa commonly occurs worldwide, thereby threatening the aquatic ecosystem and human health. In this study, four kinds of algicides were tested to explore their influence on cell density and chlorophyll-a of M. aeruginosa. Results showed that aluminum silicate agent, which inhibited more than 90% cell growth compared with the control group, demonstrated the strongest inhibition effect immediately on M. aeruginosa growth. Furthermore, the production and release of microcystin (MC)-LR were investigated. Aluminum silicate, CuSO4, and Emma-11 were more effective than pyrogallic acid in disrupting the cells of M. aeruginosa, thereby increasing the extracellular MC-LR concentration. Aluminum silicate caused the highest extracellular MC-LR concentration of more than 45 mg·L−1. Biotoxicity was also detected to evaluate the environmental risks of MC-LR release, which were related to the usages of different algicides. Extracellular MC-LR concentration mostly increased when the biotoxicity of algae solution increased. The experiments were also designed to reveal the effects of physical conditions in riverways, such as natural sunlight, aeration and benthal sludge, on MC-LR degradation. These findings indicated that UV rays in sunlight, which can achieve a MC-LR removal efficiency of more than 15%, played an important role in MC-LR degradation. Among all the physical pathways of MC-LR removal, benthal sludge adsorption presented the optimal efficiency at 20%.
Microcystis aeruginosa / MC-LR release / Algicides / MC-LR degradation / Biotoxicity
[1] |
de FigueiredoD R, AzeiteiroU M, EstevesS M, GonçalvesF J M, PereiraM J. Microcystin-producing blooms--a serious global public health issue.Ecotoxicology and Environmental Safety, 2004, 59(2): 151–163
CrossRef
Pubmed
Google scholar
|
[2] |
ShengJ, HeM, YuS, ShiH, QianY. Microcystin-LR detection based on indirect competitive enzyme-linked immunosorbent assay.Frontiers of Environmental Science & Engineering, 2007, 1(3): 329–333
CrossRef
Google scholar
|
[3] |
XiaoC B, YanH, WangJ F, WeiW, NingJ, PanG. Microcystin-LR biodegradation by Sphingopyxis sp. USTB-05.Frontiers of Environmental Science & Engineering, 2011, 5(4): 526–532
CrossRef
Google scholar
|
[4] |
OuH, GaoN, DengY, QiaoJ, WangH. Immediate and long-term impacts of UV-C irradiation on photosynthetic capacity, survival and microcystin-LR release risk of Microcystis aeruginosa.Water Research, 2012, 46(4): 1241–1250
CrossRef
Pubmed
Google scholar
|
[5] |
CoddG A. Cyanobacterial toxins: occurrence, properties and biological significance.Water Science and Technology, 1995, 32(4): 149–156
CrossRef
Google scholar
|
[6] |
MoweM A D, AbbasF, PorojanC, MitrovicS M, LimR P, FureyA, YeoD C J. Roles of nitrogen and phosphorus in growth responses and toxin production (using LC-MS/MS) of tropical Microcystis ichthyoblabe and M. flos-aquae.Journal of Applied Phycology, 2016, 28(3): 1543–1552
CrossRef
Google scholar
|
[7] |
CoddG, BellS, KayaK, WardC, BeattieK, MetcalfJ. Cyanobacterial toxins, exposure routes and human health.European Journal of Phycology, 1999, 34(4): 405–415
CrossRef
Google scholar
|
[8] |
CarmichaelW W. Cyanobacteria secondary metabolites—The cyanotoxins.Journal of Applied Bacteriology, 1992, 72(6): 445–459
CrossRef
Pubmed
Google scholar
|
[9] |
PhelanR R, DowningT G. A growth advantage for microcystin production by MicrocystisPCC7806 under high light.Journal of Phycology, 2011, 47(6): 1241–1246
CrossRef
Pubmed
Google scholar
|
[10] |
WiednerC, VisserP M, FastnerJ, MetcalfJ S, CoddG A, MurL R. Effects of light on the microcystin content of Microcystis strain PCC 7806.Applied and Environmental Microbiology, 2003, 69(3): 1475–1481
CrossRef
Pubmed
Google scholar
|
[11] |
RapalaJ, RobertsonA, NegriA P, BergK A, TuomiP, LyraC, ErkomaaK, LahtiK, HoppuK, LepistöL. First report of saxitoxin in Finnish lakes and possible associated effects on human health.Environmental Toxicology, 2005, 20(3): 331–340
CrossRef
Pubmed
Google scholar
|
[12] |
UenoY, NagataS, TsutsumiT, HasegawaA, WatanabeM F, ParkH D, ChenG C, ChenG, YuS Z. Detection of microcystins, a blue-green algal hepatotoxin, in drinking water sampled in Haimen and Fusui, endemic areas of primary liver cancer in China, by highly sensitive immunoassay.Carcinogenesis, 1996, 17(6): 1317–1321
CrossRef
Pubmed
Google scholar
|
[13] |
GuoL. Doing battle with the green monster of Taihu Lake.Science, 2007, 317(5842): 1166
CrossRef
Pubmed
Google scholar
|
[14] |
ErikssonJ E, ToivolaD, MeriluotoJ A O, KarakiH, HanY G, HartshorneD. Hepatocyte deformation induced by cyanobacterial toxins reflects inhibition of protein phosphatases.Biochemical and Biophysical Research Communications, 1990, 173(3): 1347–1353
CrossRef
Pubmed
Google scholar
|
[15] |
KotakB G, KenefickS L, FritzD L, RousseauxC G, PrepasE E, HrudeyS E. Occurrence and toxicological evaluation of cyanobacterial toxins in Alberta lakes and farm dugouts.Water Research, 1993, 27(3): 495–506
CrossRef
Google scholar
|
[16] |
FujikiH, SuganumaM. Tumor promoters—microcystin-LR, nodularin and TNF-a and human cancer development.Anti-cancer Agents in Medicinal Chemistry, 2011, 11(1): 4–18
CrossRef
Pubmed
Google scholar
|
[17] |
XuP, ZhangX X, MiaoC, FuZ, LiZ, ZhangG, ZhengM, LiuY, YangL, WangT. Promotion of melanoma cell invasion and tumor metastasis by microcystin-LR via phosphatidylinositol 3-kinase/AKT pathway.Environmental Science & Technology, 2013, 47(15): 8801–8808
Pubmed
|
[18] |
ZhangY S, ShaoY S, GaoN Y, ChuW H, SunZ W. Removal of microcystin-LR by free chlorine: identify of transformation products and disinfection by-products formation.Chemical Engineering Journal, 2015, 287: 189–195
CrossRef
Google scholar
|
[19] |
ChangJ, ChenZ L, WangZ, KangJ, ChenQ, YuanL, ShenJ M. Oxidation of microcystin-LR in water by ozone combined with UV radiation: the removal and degradation pathway.Chemical Engineering Journal, 2015, 276: 97–105
CrossRef
Google scholar
|
[20] |
LiaoW, MurugananthanM, ZhangY. Electrochemical degradation and mechanistic analysis of microcystin-LR at boron-doped diamond electrode.Chemical Engineering Journal, 2014, 243(243): 117–126
CrossRef
Google scholar
|
[21] |
ZhanJ J, ZhangQ, QinM M, HongY. Selection and characterization of eight freshwater green algae strains for synchronous water purification and lipid production.Frontiers of Environmental Science & Engineering, 2016, 10(3): 548–558
CrossRef
Google scholar
|
[22] |
ZhouS Q, ShaoY S, GaoN Y, ZhuS M, LiL, DengJ, ZhuM Q. Removal of microcystis aeruginosa by potassium ferrate (VI): impacts on cells integrity, intracellular organic matter release and disinfection by-products formation.Chemical Engineering Journal, 2014, 251(5): 304–309
CrossRef
Google scholar
|
[23] |
RodríguezE, OnstadG D, KullT P J, MetcalfJ S, AceroJ L, von GuntenU. Oxidative elimination of cyanotoxins: comparison of ozone, chlorine, chlorine dioxide and permanganate.Water Research, 2007, 41(15): 3381–3393
CrossRef
Pubmed
Google scholar
|
[24] |
WangX, UtsumiM, YangY N, ShimizuK, LiD W, ZhangZ Y, SugiuraN. Removal of microcystins (-LR, -YR, -RR) by highly efficient photocatalyst Ag/Ag3PO4 under simulated solar light condition.Chemical Engineering Journal, 2013, 230: 172–179
CrossRef
Google scholar
|
[25] |
LiaoW, ZhangY, ZhangM, MurugananthanM, YoshiharaS. Photoelectrocatalytic degradation of microcystin-LR using Ag/AgCl/TiO2 nanotube arrays electrode under visible light irradiation.Chemical Engineering Journal, 2013, 231: 455–463
CrossRef
Google scholar
|
[26] |
NicholsonB C, RositanoJ, BurchM D. Destruction of cyanobacterial peptide hepatotoxins by chlorine and chloramine.Water Research, 1994, 28(6): 1297–1303
CrossRef
Google scholar
|
[27] |
BergK, CarmichaelW W, SkulbergO M, BenestadC, UnderdallB. Investigation of a toxic water-bloom of Microcystis aeruginosa (Cyanophyceae) in Lake Akersvatn, Norway.Hydrobiologia, 1987, 144(2): 97–103
CrossRef
Google scholar
|
[28] |
SunL, LiY, LiA. Treatment of actual chemical wastewater by a heterogeneous fenton process using natural pyrite.Environment Research and Public Health, 2015, 12(11): 13762–13778
CrossRef
Pubmed
Google scholar
|
[29] |
PhoungthongK, XiaY, ZhangH, ShaoL M, HeP J. Leaching toxicity characteristics of municipal solid waste incineration bottom ash.Frontiers of Environmental Science & Engineering, 2016, 10(2): 399–411
CrossRef
Google scholar
|
[30] |
LiuY, SongL, LiX, LiuT. The toxic effects of microcystin-LR on embryo-larval and juvenile development of loach, Misguruns mizolepis Gunthe.Toxicon, 2002, 40(4): 395–399
CrossRef
Pubmed
Google scholar
|
[31] |
Kurki-HelasmoK, MeriluotoJ. Microcystin uptake inhibits growth and protein phosphatase activity in mustard (Sinapis albaL.) seedlings.Toxicon, 1998, 36(12): 1921–1926
CrossRef
Pubmed
Google scholar
|
[32] |
BøeR, GjertsenB T, VintermyrO K, HougeG, LanotteM, DøskelandS O. The protein phosphatase inhibitor okadaic acid induces morphological changes typical of apoptosis in mammalian cells.Experimental Cell Research, 1991, 195(1): 237–246
CrossRef
Pubmed
Google scholar
|
[33] |
MellgrenG, VintermyrO K, BøeR, DøskelandS O. Hepatocyte DNA replication is abolished by inhibitors selecting protein phosphatase 2A rather than phosphatase 1.Experimental Cell Research, 1993, 205(2): 293–301
CrossRef
Pubmed
Google scholar
|
/
〈 | 〉 |