Effects of cadmium on mineral metabolism and antioxidant enzyme activities in Salix matsudana Koidz

• Autorzy: Zou J. , Shang X. , Li C. , Ouyang J. , Li B. , Liu X.
• Języki publikacji: EN

Abstrakty

EN

Salix matsudana Koidz was exposed to different concentrations of Cd (0, 10, 50, and 100 µmol/L) to study the effects of Cd on mineral metabolism and antioxidant enzyme activities. The results showed that plant height and root length were inhibited by 50 and 100 µmol/L Cd, except the one under 10 µmol/L Cd treatment. The Cd content accumulated in different organs of S. matsudana, gradually increasing with increased Cd concentrations and prolonged treatment times. The root was the main organ for absorbing and accumulating Cd. Cd inhibited the accumulation of Fe, Zn, Mn, and Cu. In addition, the activities of antioxidant enzymes and the contents of reactive oxygen species were also changed by different concentrations of Cd. The results obtained here can provide scientific and objective data for the use of S. matsudana in the remediation of Cd-contaminated soil.

• Wydawca: -
• Czasopismo: Polish Journal of Environmental Studies
• Rocznik: 2019
• Tom: 28
• Numer: 2
• Opis fizyczny: p.989-999,fig.,ref.

Twórcy

autor

Zou J.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

autor

Shang X.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

autor

Li C.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

autor

Ouyang J.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

autor

Li B.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

autor

Liu X.

• Tianjin Key Laboratory of Animal and Plant Resistance, College of Life Sciences, Tianjin Normal University, Tianjin, China

Bibliografia

• 1. ELOBEID M., GOBEL C., FEUSSNER I., POLLE A. Cadmium interferes with auxin physiology and lignification in poplar. J. Exp. Bot. 63, 1413, 2012.
• 2. ERMAKOV V.V, PETRUNINA N.S., TYUTIKOV S.F., DANILOVA V.N., KHUSHVAKHTOVA S.D., DEGTYAREV A.P., KRECHETOVA E.V. Concentrating metals by plants of the genus Salix and their importance for identification of Cd anomalies. Geochemistry International, 53, 951, 2015.
• 3. MARTÍNEZ-LÓPEZ S., MARTÍNEZ-SÁNCHEZ M.J., PÉREZ-SIRVENT C., BECH J., GÓMEZ MARTINEZ M.C., GARCÍA-FERNANDEZ A.J. Screening of wild plants for use in the phytoremediation of mining-influenced soils containing arsenic in semiarid environments. J. Soils Sediments 14, 794, 2014.
• 4. YANG J.X., LI X.L., HU Y.B., GAO L.M., YAO D.X. Enrichment Characteristics of heavy metal cadmium in woody plants system. Kem. Ind. 64, 283, 2015.
• 5. EKMEKCI Y., TANYOLAC D., AYHAN B. Effects of cadmium on antioxidant enzyme and photosynthetic activities in leaves of two maize cultivars. J. Plant Physiol. 165, 600, 2008.
• 6. ZOU J.H., WANG G., JI J., WANG J.Y., WU H.F., OU Y.J., LI B.B. Transcriptional, physiological and cytological analysis validated the roles of some key genes linked Cd stress in Salix matsudana Koidz. Environ. Experi. Bot. 134, 116, 2017.
• 7. IORI V., ZACCHINI M., PIETRINI F. Growth, physiological response and phytoremoval capability of two willow clones exposed to ibuprofen under hydroponic culture. J. Hazard. Mater 262, 796, 2013.
• 8. HERNÁNDEZ J.A., JIMÉNEZ A., MULLINEAUX P., SEVILLA F. Tolerance of pea (Pisum sativum L.) to longterm salt stress is associated with induction of antioxidant defenses. Plant Cell Environ. 23, 853-862, 2000.
• 9. DINAKAR C., ABHAYPRATAP V., YEARLA S.R., RAGHAVENDRA A.S., PADMASREE K. Importance of ROS and antioxidant system during the beneficial interactions of mitochondrial metabolism with photosynthetic carbon assimilation. Planta 231, 461, 2010.
• 10. JIA Y., TANG S.R., WANG R.G., JU X.H., DING Y.Z., TU S.X., SMITH D.L. Effects of elevated CO2 on growth, photosynthesis, elemental composition, antioxidant level, and phytochelatin concentration in Lolium mutiforum and Lolium perenne under Cd stress. J. Hazard. Mater. 180, 384, 2010.
• 11. JIN C.W., MAO Q.Q., LUO B.F., LIN X.Y., DU S.T. Mutation of mpk6 enhances cadmium tolerance in Arabidopsis plants by alleviating oxidative stress. Plant Soil 371, 387, 2013.
• 12. DAT J.F., VANDENABEELE S., VRANOVA E., VAN M.M., INZE D., VANBREUSEGEM F. Dual action of the active oxygen species during plant stress responses. Cell Mol. Life Sci. 57, 779, 2000.
• 13. WU H.F., WANG J.Y., OU Y.J., JIANG W.S., LIU D.H., ZOU J.H. Characterisation of early responses to cadmium in roots of Salix matsudana Koidz [J]. Toxicol. Environ. Chem. 99, 913, 2017.
• 14. WU H.F., WANG J.Y., LI B.B., ZOU J.H. Salix matsudana Koidz tolerance mechanisms to cadmium: uptake and accumulation, subcellular distribution, and chemical forms [J]. Pol. J. of Environ. Stud. 25, 1739, 2016.
• 15. ZOU J.H., YUE J.Y., JIANG W.S., LIU D.H. Effects of cadmium stress on root tip cells and some physiological indexes in Allium cepa var. agrogarum L. Acta Biol. Cracov. Bot. 54, 129, 2012.
• 16. LUX A., MARTINKA M., VACULIK M., WHITE P.J. Root responses to cadmium in the rhizosphere: a review. J. Exp. Bot. 62, 21, 2011.
• 17. ZACCHINI M., PIETRINI F., MUGNOZZA G.S., IORI V., PIETROSANTI L., MASSACCI A. Metal tolerance, accumulation and translocation in poplar and willow clones treated with cadmium in hydroponics.Water Air Soil Poll. 197, 23, 2009.
• 18. VONDRÁČKOVÁ S., TLUSTOŠ P., HEJCMAN M., SZÁKOVÁ J. Regulation of macro, micro, and toxic element uptake by Salix × smithiana using liming of heavily contaminated soils. J. Soils Sediments 17, 1279, 2017.
• 19. BAKER A.J.M., BROOKS R.R., BAKER N.A. Terrestrial higher plants which hyperaccumulate metallic elements - a review of their distribution, ecology and phytochemistry. ScienceOpen Inc., Boston, 81, 1989.
• 20. BAKER A.J.M., WHITING S.N. In search of the Holy Grail - a further step in understanding metal hyperaccumulation? New Phytol. 155, 1, 2002.
• 21. POLLARD A.J., POWELL K.D., HARPER F.A., SMITH J.A.C. The genetic basis of metal hyperaccumulation in plants. Crit. Rev. Plant Sci. 21, 539, 2002.
• 22. BAKER A.J.M., MCGRATH S.P., REEVES R.D., SMITH J.A.C. Metal hyperaccumulator plants: a review of the ecology and physiology of a biological resource for phytoremediation of metal-polluted soils. In: Terry, N., Bañuelos, G.S. (Eds.), Phytoremediation of Contaminated Soil and Water. CRC Press Inc., Boca Raton, FL, USA, 857, 2000.
• 23. ZÁRUBOVÁ P., HEJCMAN M., VONDRÁČKOVÁ S., MRNKA L., SZÁKOVÁ J., TLUSTOŠ P. Distribution of P, K, Ca, Mg, Cd, Cu, Fe, Mn, Pb and Zn in wood and bark age classes of willows and poplars used for phytoextraction on soils contaminated by risk elements. Environ. Sci. Pollut. R. 22, 18801, 2015.
• 24. CLEMENS S. Molecular mechanisms of plant metal tolerance and homeostasis. Planta 212, 475, 2001.
• 25. CLEMENS S., PALMGREN M.G., KRÄMER U. A long way ahead: understanding and engineering plant metal accumulation.Trends Plant Sci. 7, 309, 2002.
• 26. SEBASTIANI L., SCEBBA F., TOGNETTI R. Heavy metal accumulation and growth responses in poplar clones Eridano (Populus deltoides × maximowiczii) and I-214 (P. × euramericana) exposed to industrial waste. Environ. Exp. Bot. 52, 79, 2004.
• 27. ASTOLFI S., ORTOLANIA M.R., CATARCIONEA G., PAOLACCIA A.R., CESCOB S., PINTON R., CIAFFI M. Cadmium exposure affects iron acquisition in barley (Hordeum vulgare) seedlings. Physiol. Plantarum 152, 646, 2014.
• 28. MIKKELSEN M.D., PEDAS P., SCHILLER M., VINCZE E., MILLS.R.F., BORG S., MOLLER A., SCHJOERRING J.K., WILLIAMS L.E., BAEKGAARD L., HOLM P.B., PALMGREN M.G. Barley HvHMA1 is a heavy metal pump involved in mobilizing organellar Zn and Cu and plays a role in metal loading into grains. Plos One 7, e49027, 2012.
• 29. DUBEY R.S. Metal toxicity, oxidative stress and antioxidative defense system in plants. In: Gupta SD (ed) Reactive oxygen species and antioxidants in higher plants. Science Publishers, CRC Press,Taylor and Francis Group, USA, 177, 2010.
• 30. GALLEGO S.M., PENA L.B., BARCIA R.A., AZPILICUETA C.E., IANNONE M.F., ROSALES E.P., ZAWOZNIK M.S., GROPPA M.D., BENAVIDES M.P. Unravelling cadmium toxicity and tolerance in plants: insight into regulatory mechanisms. Environ. Exp. Bot. 83, 33, 2012.
• 31. SHARMA P., JHA A.B., DUBEY R.S., PESSARAKLI M. Reactive oxygen species, oxidative damage, and antioxidative defense mechanism in plants under stressful conditions. J Bot. 2012, 217037, 2012.
• 32. LI D.D., ZHOU D.M., WANG P., WENG N.Y., ZHU X.D. Subcellular Cd distribution and its correlation with antioxidant enzymatic activities in wheat (Triticum aestivum) roots. Ecotox. Environ. Safe 74, 874, 2011.

Identyfikatory

DOI

10.15244/pjoes/81697