Home Accumulation and physiological response of cadmium in Hydrocharis dubia
Article
Licensed
Unlicensed Requires Authentication

Accumulation and physiological response of cadmium in Hydrocharis dubia

  • Haiyan Yang , Wenlong Wu EMAIL logo , Weilin Li and Guoxin Shi
Published/Copyright: February 28, 2017
Become an author with De Gruyter Brill

Abstract

The effects of increasing concentrations of cadmium (Cd) on the ultrastructure, Cd accumulation, nutrient elements contents, levels of chlorophyll pigments, hydrogen peroxide (H2O2), malondialdehyde (MDA), antioxidants, as well as the activities of antioxidant enzymes were investigated in the leaves of Hydrocharis dubia (Bl.) Backer. Cd exposure resulted in significant damage in chloroplasts and mitochondria, suggesting that Cd hastened the senescence of the tested plants. The accumulation of Cd was found to increase in a concentration dependent manner with a maximum of 1088 μg g−1 at 80 μM. The levels of Ca, P and Cu declined and the levels of Mg increased under all Cd concentrations, but K and Fe contents increased initially and decreased thereafter. Pigment content decreased with the rise of the Cd concentrations. H2O2 content enhanced gradually at all Cd concentrations. MDA content increased progressively up to 60 μM Cd, followed by a decline at higher concentration. The effect of Cd application on ascorbate (AsA) and reduced glutathione (GSH) contents was similar to that seen for H2O2 content. Peroxidase (POD) and catalase (CAT) activities first increased and then decreased, while superoxide dismutase (SOD) activity markedly decreased. Results suggest that Cd-induced oxidative damage in H. dubia is closely associated with the efficiency of its intrinsic antioxidant mechanisms, both the disorder of nutrient elements and the damage to the ultrastructure were indicative of general disarray in the cellular functions exerted by Cd.

Acknowledgements

The research was supported in part by the grant from Jiangsu Agricultural Science and Technology Innovation Fund Project (No.CX(16)1035).

References

Alscher R.G., Erturk N. & Heath L.S. 2002. Role of superoxide dismutases (SODs) in controlling oxidative stress in plants. J. Exp. Bot. 53: 1331–1341.10.1093/jexbot/53.372.1331Search in Google Scholar

Anderson M.E. 1985. Determination of glutathione and glutathione disulfide in biological samples. Methods Enzymol 113: 545–548.10.1016/S0076-6879(85)13073-9Search in Google Scholar

Austin J.R., Frost E., Vidi P.A., Kessler F. & Stehelin L. 2006. Plastoglobules are lipoprotein subcompartments of the chloroplast that are permanently coupled to thylakoid membranes and contain biosynthetic enzymes. Plant Cell 18: 1693–1703.10.1105/tpc.105.039859Search in Google Scholar

Benavides M.P., Gallego S.M. & Tomaro M.L. 2005. Cadmium toxicity in plants. Braz. J. Plant Physiol. 17: 21–34.10.1590/S1677-04202005000100003Search in Google Scholar

Chaoui A., Mazhoudi S., Ghorbal M.H. & Ferjana E.E. 1997. Cadmium and zinc induction of lipid peroxidation and effects on antioxidant enzyme activities in bean (Phaseolus vulgaris L.). Plant Sci. 127: 139–147.10.1016/S0168-9452(97)00115-5Search in Google Scholar

Ding B.Z., Shi G.X., Xu Y., Hu J.Z. & Xu Q.S. 2007. Physiological responses of Alternanthera philoxeroides (Mart.) Griseb leaves to cadmium stress. Environ. Pollut. 147: 800–803.10.1016/j.envpol.2006.10.016Search in Google Scholar PubMed

Dong J., Wu F.B. & Zhang G.P. 2006. Influence of cadmium on antioxidant capacity and four microelement concentrations in tomato seedlings (Lycopersicon esculentum). Chemosphere 64: 1659–1666.10.1016/j.chemosphere.2006.01.030Search in Google Scholar PubMed

Douchiche O., Soret-Morvan O., Chadbi W., Morvan C. & Paynel F. 2010. Characteristics of cadmium tolerance in ‘Hermes’ flax seedlings: contribution of cell walls. Chemosphere 81: 1430–1436.10.1016/j.chemosphere.2010.09.011Search in Google Scholar PubMed

Elloumi N., Zouari M., Chaari L., Jomni C., BenRouina B. & BenAbdallah F. 2014. Ecophysiological responses of almond (Prunus dulcis) seedlings to cadmium stress. Biologia 69: 604–609.10.2478/s11756-014-0348-xSearch in Google Scholar

Fatima R.A. & Ahmad M. 2005. Certain antioxidant enzymes of Allium cepa as biomarkers for the detection of toxic heavy metals in wastewater. Sci. Total Environ. 346: 256–273.10.1016/j.scitotenv.2004.12.004Search in Google Scholar PubMed

Foyer C.H. & Noctor G. 2005. Redox homeostasis and antioxidant signaling: a metabolic interface between stress perception and physiological responses. Plant Cell 17: 1866–1875.10.1105/tpc.105.033589Search in Google Scholar

Ghnaya T., Slama I., Messedi D., Grignon C., Ghorbel M.H. & Abdelly C. 2007. Effects of Cd2+ on K+, Ca2+ and N Uptake in Two Halophytes Sesuvium portulacastrum and Mesembryanthemum crystallinum: Consequences on Growth. Chemosphere 67: 72–79.10.1016/j.chemosphere.2006.09.064Search in Google Scholar

Góth L. 1991. A simple method for determination of serum catalase activity and revision of reference range. Clin. Chim. Acta 196: 143–152.10.1016/0009-8981(91)90067-MSearch in Google Scholar

Groppa M.D., Tomaro M.L. & Benavides M.P. 2001. Polyamines as protectors against cadmium or copper-induced oxidative damage in sunflower leaf discs. Plant Sci. 161: 481–488.10.1016/S0168-9452(01)00432-0Search in Google Scholar

Khan S. Chao C., Waqas M., Arp H.P.H. & Zhu Y.G. 2013. Sewage sludge biochar influence upon rice (Oryza sativa L) yield, metal bioaccumulation and greenhouse gas emissions from acidic paddy soil. Environ. Sci. Technol. 47: 8624–8632.10.1021/es400554xSearch in Google Scholar

Law M.Y., Charles S.A. & Halliwell B. 1983. Glutathione and ascorbic acid in spinach (Spinacia oleracea) chloroplasts. The effect of hydrogen peroxide and of paraquat. Biochem. J. 210: 899–903.10.1042/bj2100899Search in Google Scholar

Liang T.S., Ding H., Wang G.D., Kang J.Q., Pang H.X. & Lv J.Y. 2016. Sulfur decreases cadmium translocation and enhances cadmium tolerance by promoting sulfur assimilation and glutathione metabolism in Brassica chinensis L. Ecotox. Environ. Safe 124: 129–137.10.1016/j.ecoenv.2015.10.011Search in Google Scholar

Lichtenthaler H.K. 1987. Chlorophylls and Carotenoids: Pigments of Photosynthetic Membranes. Methods Enzymol. 148: 350–382.10.1016/0076-6879(87)48036-1Search in Google Scholar

Liu Y.G., Wang X., Zeng G.M., Qu D., Gu J.J., Zhou M. & Chai L.Y. 2007. Cadmium-induced oxidative stress and response of the ascorbate–glutathione cycle in Bechmeria nivea (L.) Gaud. Chemosphere 69: 99–107.10.1016/j.chemosphere.2007.04.040Search in Google Scholar PubMed

Liu Z.L., He X.Y., & Chen W. 2011. Effects of cadmium hyperaccumulation on the concentrations of four trace elements in Lonicera japonica Thunb. Ecotoxicology 20: 698–705.10.1007/s10646-011-0609-1Search in Google Scholar PubMed

Maehly A.C. 1955. Plant peroxidase. Methods Enzymol 2: 801–813.10.1016/S0076-6879(55)02307-0Search in Google Scholar

Mishra S., Srivastava S., Tripathi R.D., Govindarajan R., Kuriakose S.V. & Prasad M.N.V. 2006. Phytochelatin synthesis and response of antioxidants during cadmium stress in Bacopa monnieri L. Plant Physiol. Biochem. 44: 25–37.10.1016/j.plaphy.2006.01.007Search in Google Scholar PubMed

Monteiro M.S., Santos C., Soares A.M.V.M. & Mann R.M. 2009. Assessment of biomarkers of cadmium stress in lettuce. Ecotox. Environ. Safe 7: 811–818.10.1016/j.ecoenv.2008.08.002Search in Google Scholar PubMed

Mobin M. & Khan N.A. 2007. Photosynthetic activity, pigment composition and antioxidative response of two mustard (Brassica juncea) cultivars differing in photosynthetic capacity subjected to cadmium stress. J. Plant Physiol. 164: 601–610.10.1016/j.jplph.2006.03.003Search in Google Scholar PubMed

Parmar P., Kumari N. & Sharma V. 2013. Structural and functional alterations in photosynthetic apparatus of plants under cadmium stress. Bot. Stud. 54: 45.10.1186/1999-3110-54-45Search in Google Scholar PubMed PubMed Central

Singh S., Eapen S. & D’Souza S.F. 2006. Cadmium accumulation and its influence on lipid peroxidation and antioxidative system in an aquatic plant, Bacopa monnieri L. Chemosphere 62: 233–246.10.1016/j.chemosphere.2005.05.017Search in Google Scholar PubMed

Srivastava S., Tripathi R.D. & Dwivedi U.N. 2004. Synthesis of phytochelatins and modulation of antioxidants in response to cadmium stress in Cuscuta reflexa - An angiospermic parasite. J. Plant Physiol. 161: 665–674.10.1078/0176-1617-01274Search in Google Scholar PubMed

Stewert R.C. & Bewley J.D. 1980. Lipid peroxidation associated with accelerated aging of soybean axes. Plant Physiol. 65: 45–248.10.1104/pp.65.2.245Search in Google Scholar PubMed PubMed Central

Sun Q., Ye Z.H., Wang X.R. & Wong M.H. 2007. Cadmium hyperaccumulation leads to an increase of glutathione rather than phytochelatins in the cadmium hyperaccumulator Sedum alfredii. J. Plant Physiol. 164: 1489–1498.10.1016/j.jplph.2006.10.001Search in Google Scholar PubMed

Szőllősi R., Varga I.S., Erdei L. & Mihalik E.B. 2009. Cadmiuminduced oxidative stress and antioxidative mechanisms in germinating Indian mustard (Brassica juncea L.) seeds. Ecotox. Environ. Safe 72: 1337–1342.10.1016/j.ecoenv.2009.04.005Search in Google Scholar PubMed

Wang X., Shi G.X., Xu Q.S. & Hu J.Z. 2007. Exogenous polyamines enhance copper tolerance of Nymphoides peltatum. J. Plant Physiol. 164: 1062–1070.10.1016/j.jplph.2006.06.003Search in Google Scholar PubMed

Xu Q.S., Hu J.Z., Xie K.B., Yang H.Y., Du K.H. & Shi G.X. 2010. Accumulation and acute toxicity of silver in Potamogeton crispus L. J. Hazard Mater. 173: 186–193.10.1016/j.jhazmat.2009.08.067Search in Google Scholar PubMed

Received: 2016-5-18
Accepted: 2016-11-29
Published Online: 2017-2-28
Published in Print: 2017-2-1

© 2017 Institute of Botany, Slovak Academy of Sciences

Downloaded on 10.10.2025 from https://www.degruyterbrill.com/document/doi/10.1515/biolog-2017-0013/html
Scroll to top button