Uso de Myriophyllum aquaticum para inibir o crescimento de Microcystis aeruginosa e remover microcistina-LR

Autores

DOI:

https://doi.org/10.5327/Z2176-94781309

Palavras-chave:

alelopatia; cianobactérias; cianotoxinas; macrófitas aquáticas submersas; soluções baseadas na natureza.

Resumo

Florações de cianoabactérias são consideradas um dos maiores desafios na preservação de fontes hídricas, especialmente quando estão presentes espécies como Microcystis aeruginosa. A descoberta de alternativas de remediação faz-se necessária, e uma delas é o uso de macrófitas aquáticas, como as espécies do gênero Myriophyllum, que apresentam atividades alelopáticas para o controle fitoplanctônico. Diante disso, este trabalho teve como objetivos avaliar a inibição do crescimento de células de M. aeruginosa em uma coexposição com Myriophyllum aquaticum e avaliar a remoção de microcistina-LR. Os experimentos foram conduzidos com cultivos de M. aeruginosa (1x106células mL-1) em coexposição com M. aquaticum por sete dias. Os efeitos inibitórios foram investigados por contagem celular. Os efeitos nos pigmentos fotossintéticos foram mensurados, além da quantificação de microcistina-LR no último dia experimental. Para avaliar possíveis efeitos de competição por nutrientes e espaço, realizou-se a quantificação da concentração de ortofosfato total e utilizou-se um tratamento com planta de plástico. Os experimentos com M. aquaticum apresentaram inibição total do crescimento de M. aeruginosa e redução significativa na concentração dos pigmentos fotossintéticos (> 98%). Além disso, foi constatada redução na concentração de microcistina-LR (79%) nos testes com macrófitas quando comparadas ao grupo controle. Não foi observada competição por espaço e nutrientes, o que demonstra que os efeitos sobre M. aeruginosa foram causados pela presença da macrófita aquática. Dessa forma, estes resultados podem demonstrar que M. aquaticum gerou a inibição no crescimento de cianobactérias por efeitos alelopáticos, além de remover a microcistina-LR das águas.

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Referências

Almeida, A.R.D.; Passig, F.H.; Pagioro, T.A.; Nascimento, P.T.H.D.; Carvalho, K.Q.D., 2016. Remoção de microcistina-LR da Microcystis aeruginosa utilizando bagaço de cana-de-açúcar in natura e carvão ativado. Revista Ambiente & Água, v. 11(1), 188-197. https://doi.org/10.4136/ambi-agua.1785.

Calado, S.L.M.; Esterhuizen-Londt, M.; Silva de Assis, H.C.; Pflugmacher, S., 2019. Phytoremediation: green technology for the removal of mixed contaminants of a water supply reservoir. International Journal of Phytoremediation, v. 21, (4), 372-379. http://doi.org/10.1080/15226514.2018.1524843.

Chapman, D.J.; Kremer, B.P. 1988. Experimental phycology: a laboratory manual. Cambridge: Cambridge University Press, 308 pp.

Chen, J.Q.; Guo, R.X., 2014. Inhibition effect of green alga on cyanobacteria by the interspecies interactions. International Journal of Environmental Science and Technology, v. 11, (3), 839-842. https://doi.org/10.1007/s13762-013-0208-1.

Cheng, W.; Xuexiu, C.; Hongjuan, D.; Difu, L.; Junyan, L., 2008. Allelopathic inhibitory effect of Myriophyllum aquaticum (Vell.) Verdc. on Microcystis aeruginosa and its physiological mechanism. Acta Ecologica Sinica, v. 28, (6), 2595-2603. https://doi.org/10.1016/S1872-2032(08)60061-X.

Ferreira, T.F.; Crossetti, L.O.; Marques, D.M.M.; Cardoso, L.; Fragoso Jr., C.R.; van Nes, E.H., 2018. The structuring role of submerged macrophytes in a large subtropical shallow lake: Clear effects on water chemistry and phytoplankton structure community along a vegetated-pelagic gradient. Limnologica, v. 69, 142-154. https://doi.org/10.1016/j.limno.2017.12.003.

Gorham, P.R.; McLachlav, J.R.; Hammer, V.T.; Kim, W.K., 1964. Isolation culture of toxic strains of Anabaena flos-aquae (Lyngb.) Internationale Vereinigung für theoretische und angewandte Limnologie: Verhandlungen. v. 15, (2), 796-804. https://doi.org/10.1080/03680770.1962.11895606.

Gross, E.M. 2003. Differential response of tellimagrandin II and total bioactive hydrolysable tannins in an aquatic angiosperm to changes in light and nitrogen. Oikos, v. 103, (3), 497-504. https://doi.org/10.1034/j.1600-0706.2003.12666.x.

Gross, E.M.; Meyer, H.; Schilling, G., 1996. Release and ecological impact of algicidal hydrolysable polyphenols in Myriophyllum spicatum. Phytochemistry, v. 41, (1), 133-138. https://doi.org/10.1016/0031-9422(95)00598-6.

Huang, S.; Zhu, J.; Zhang, L.; Peng, X.; Zhang, X.; Ge, F.; Liu, B.; Wu, Z., 2020. Combined Effects of Allelopathic Polyphenols on Microcystis aeruginosa and Response of Different Chlorophyll Fluorescence Parameters. Frontiers in Microbiology, v. 11, 614570. https://doi.org/10.3389%2Ffmicb.2020.614570.

Kakade, A.; Salama, E.S.; Han, H.; Zheng, Y.; Kulshrestha, S.; Jalalah, M.; Harraz, F.A.; Alsareii, S.A.; Li, X., 2021. World eutrophic pollution of lake and river: Biotreatment potential and future perspectives. Environmental Technology & Innovation, v. 23, 101604. https://doi.org/10.1016/j.eti.2021.101604.

Kitamura, R.S.A.; Silva, A.R.; Pagioro, T.A.; Martins, L.R.R., 2021. Bioatividade alelopática de extratos metanólicos de Myriophyllum aquaticum (Vell.) Verdc. sobre Microcystis aeruginosa. Enciclopédia Biosfera, v. 18, (37), 116-128. https://doi.org/10.18677/EnciBio_2021C10.

Kudela, R.M.; Palacios, S.L.; Austerberry, D.C.; Accorsi, E.K.; Guild, L.S.; Torres-Perez, J., 2015. Application of hyperspectral remote sensing to cyanobacterial blooms in inland waters. Remote Sensing of Environment, v. 167, 196-205. https://doi.org/10.1016/j.rse.2015.01.025.

Leu, E.; Krieger-Liszkay, A.; Goussias, C.; Gross, E.M., 2002. Polyphenolic allelochemicals from the aquatic angiosperm Myriophyllum spicatum inhibit photosystem II. Plant Physiology, v. 130, (4), 2011-2018. https://doi.org/10.1104/pp.011593.

Li, B.; Yin, Y.; Kang, L.; Feng, L.; Liu, Y.; Du, Z.; Tian, Y.; Zhang, L. 2021. A review: Application of allelochemicals in water ecological restoration – algal inhibition. Chemosphere, v. 267, 128869. https://doi.org/10.1016/j.chemosphere.2020.128869.

Li, J.; Liu, Y.; Zhang, P.; Zeng, G.; Cai, X.; Liu, S.; Yin, Y.; Hu, X; Tan, X., 2016. Growth inhibition and oxidative damage of Microcystis aeruginosa induced by crude extract of Sagittaria trifolia tubers. Journal of Environmental Sciences, v. 43, 40-47. https://doi.org/10.1016/j.jes.2015.08.020.

Lichtenthaler, H.K.; Wellburn, A.R., 1983. Determinations of total carotenoids and chlorophylls a and b of leaf extracts in different solvents. Biochemical Society Transactions, v. 11, (5), 591-592. https://doi.org/10.1042/bst0110591.

Lu, Z.; Sha, J.; Tian, Y.; Zhang, X.; Liu, B.; Wu, Z., 2017. Polyphenolic allelochemical pyrogallic acid induces caspase-3 (like)-dependent programmed cell death in the cyanobacterium Microcystis aeruginosa. Algal Research, v. 21, 148-155. https://doi.org/10.1016/j.algal.2016.11.007.

McColl, R., 2018. Phycobiliproteins. California: CRC Press, 224 p.

Meng, P.; Pei, H.; Hu, W.; Liu, Z.; Li, X.; Xu, H., 2015. Allelopathic effects of Alianthus altissima extracts on Microcystis aeruginosa growth, physiological changes and microcystins release. Chemosphere, v. 141, 219-226. https://doi.org/10.1016/j.chemosphere.2015.07.057.

Mohamed, Z.A., 2017. Macrophytes-cyanobacteria allelopathic interactions and their implications for water resources management: a review. Limnologica, v. 63, 122-132. https://doi.org/10.1016/j.limno.2017.02.006.

Munoz, M.; Cirés, S.; Pedro, Z.M.; Colina, J.Á.; Velásquez-Figueroa, Y.; Carmona-Jiménez, J.; Caro-Borrero, A.; Salazar, A.; Fuster, M.S.M.; Contreras, D.; Perona, E.; Quesada, A.; Casas, J.A., 2021. Overview of toxic cyanobacteria and cyanotoxins in Ibero-American freshwaters: challenges for risk management and opportunities for removal by advanced technologies. Science of the Total Environment, v. 761, 143197. https://doi.org/10.1016/j.scitotenv.2020.143197.

Nakai, S.; Zou, G.; Okuda, T.; Nishijima, W.; Hosomi, M.; Okada, M., 2012. Polyphenols and fatty acids responsible for anti-cyanobacterial allelopathic effects of submerged macrophyte Myriophyllum spicatum. Water Science and Technology, v. 66, (5), 993-999. https://doi.org/10.2166/wst.2012.272.

Pflugmacher, S.; Kühn, S.; Lee, S.H.; Choi, J.W.; Baik, S.; Kwon, K.S.; Contardo-Jara, V., 2015. Green Liver Systems® for water purification: using the phytoremediation potential of aquatic macrophytes for the removal of different cyanobacterial toxins from water. American Journal of Plant Sciences, v. 6, (9), 1607-1618. https://doi.org/10.4236/ajps.2015.69161.

Qian, Y.; Xu, N.; Liu, J.; Tian, R., 2018. Inhibitory effects of Pontederia cordata on the growth of Microcystis aeruginosa. Water Science and Technology, v. 2017, (1), 99-107. https://doi.org/10.2166/wst.2018.090.

Ramya, M.; Umamaheswari, A.; Elumalai, S., 2020. Global health concern of cyanotoxins in surface water and its various detection methods. Current Botany, v. 11, 65-74. https://doi.org/10.25081/cb.2020.v11.6059.

Tanvir, R.U.; Hu, Z.; Zhang, Y.; Lu, J., 2021. Cyanobacterial community succession and associated cyanotoxin production in hypereutrophic and eutrophic freshwaters. Environmental Pollution, v. 290, 118056. https://doi.org/10.1016/j.envpol.2021.118056

Tazart, Z.; Caldeira, A.T.; Douma, M.; Salvador, C.; Loudiki, M., 2021. Inhibitory effect and mechanism of three macrophytes extract on Microcystis aeruginosa growth and physiology. Water and Environment Journal, v. 35, (2), 580-592. https://doi.org/10.1111/wej.12653.

Torres, M.A.; Micheletto, J.; Liz, M.V.; Pagioro, T.A.; Martins, L.R.R.; Freitas, A.M. 2020. Microcystis aeruginosa inactivation and microcystin-LR degradation by the photo-Fenton process at the initial near-neutral pH. Photochemical & Photobiological Sciences, v. 19, (10), 1470-1477. https://doi.org/10.1039/d0pp00177e.

Touzet, N.; McCarthy, D.; Gill, A.; Fleming, G.T.A., 2016. Comparative summer dynamics of surface cyanobacterial communities in two connected lakes from the west of Ireland. Science of the Total Environment, v. 553, 416-428. https://doi.org/10.1016/j.scitotenv.2016.02.117.

Valderrama, J.C., 1981. The simultaneous analysis of total nitrogen and total phosphorus in natural waters. Marine Chemistry, v. 10, (2), 109-122. https://doi.org/10.1016/0304-4203(81)90027-X.

Wang, H.; Liu, F.; Luo, P.; Li, Z.; Zheng, L.; Wang, H.; Zou, D.; Wu, J., 2017a. Allelopathic effects of Myriophyllum aquaticum on two cyanobacteria of Anabaena flos-aquae and Microcystis aeruginosa. Bulletin of environmental contamination and toxicology, v. 98, (4), 556-561. https://doi.org/10.1007/s00128-017-2034-5.

Wang, H.Q.; Zhang, L.Y.; Fang, X.M.; Zhang, A.N. 2017b. Modified water treatment residual as flocculant for Microcystis aeruginosa removal and water purification. International Journal of Environmental Science and Technology, v. 14 (11), 2543-2550. https://doi.org/10.1007/s13762-017-1381-4.

Zohdi, E.; Abbaspour, M., 2019. Harmful algal blooms (red tide): a review of causes, impacts and approaches to monitoring and prediction. International Journal of Environmental Science and Technology, v. 16, (3), 1789-1806. https://doi.org/10.1007/s13762-018-2108-x.

Zhu, J.; Liu, B.; Wang, J.; Gao, Y.; Wu, Z., 2010. Study on the mechanism of allelopathic influence on cyanobacteria and chlorophytes by submerged macrophyte (Myriophyllum spicatum) and its secretion. Aquatic Toxicology, v. 98, (2), 196-203. https://doi.org/10.1016/j.aquatox.2010.02.011.

Zhu, X.; Dao, G.; Tao, Y.; Zhan, X.; Hu, H., 2021. A review on control of harmful algal blooms by plant-derived allelochemicals. Journal of Hazardous Materials, v. 401, 123403. https://doi.org/10.1016/j.jhazmat.2020.123403.

Publicado

06-09-2022

Como Citar

Kitamura, R. S. A., da Silva, A. R. S., Pagioro, T. A., & Martins, L. R. R. (2022). Uso de Myriophyllum aquaticum para inibir o crescimento de Microcystis aeruginosa e remover microcistina-LR. Revista Brasileira De Ciências Ambientais, 57(3), 434–441. https://doi.org/10.5327/Z2176-94781309

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