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Cadmium uptake by the water hyacinth: Effects of root mass, solution volume, complexers and other metal ions1

dc.contributor.authorHardy, James K.en_US
dc.contributor.authorO'Keeffe, David H.en_US
dc.date.accessioned2006-04-07T19:15:05Z
dc.date.available2006-04-07T19:15:05Z
dc.date.issued1985en_US
dc.identifier.citationHardy, James K., O'Keeffe, David H. (1985)."Cadmium uptake by the water hyacinth: Effects of root mass, solution volume, complexers and other metal ions1." Chemosphere 14(5): 417-426. <http://hdl.handle.net/2027.42/25899>en_US
dc.identifier.urihttp://www.sciencedirect.com/science/article/B6V74-488882M-20/2/1d40863719c53ab7d8613ebc5d5a624ben_US
dc.identifier.urihttps://hdl.handle.net/2027.42/25899
dc.description.abstractAt a fixed Cd2+ concentration water hyacinth () plants with greater root mass (dry weight) take up more metal ions as a function of time, and more metal ions are taken up by a plant as the solution volume is increased. Experiments in which several different metal ion complexers were present suggest that (1) the roots possess sites which initially reversibly bind free Cd2+, (2) some added complexers can compete with these root sites for free Cd2+, and (3) with time Cd2+ bound to the roots is translocated into into the root tissues effectively removing it from the equilibrium processes in solution. Many metal ions are taken up by the plant but only the micronutrient Zn2+ competes well with Cd2+ for uptake. Thus, there may be binding sites on the roots for specific metal ions.en_US
dc.format.extent477652 bytes
dc.format.extent3118 bytes
dc.format.mimetypeapplication/pdf
dc.format.mimetypetext/plain
dc.language.isoen_US
dc.publisherElsevieren_US
dc.titleCadmium uptake by the water hyacinth: Effects of root mass, solution volume, complexers and other metal ions1en_US
dc.typeArticleen_US
dc.rights.robotsIndexNoFollowen_US
dc.subject.hlbsecondlevelNatural Resources and Environmenten_US
dc.subject.hlbsecondlevelEcology and Evolutionary Biologyen_US
dc.subject.hlbtoplevelScienceen_US
dc.description.peerreviewedPeer Revieweden_US
dc.contributor.affiliationumDepartment of Chemistry The University of Michigan-Flint, Flint, MI 48503, USAen_US
dc.contributor.affiliationotherDepartment of Chemistry and the Center for Environmental Studies The University of Akron, Akron, OH 44325, USAen_US
dc.description.bitstreamurlhttp://deepblue.lib.umich.edu/bitstream/2027.42/25899/1/0000462.pdfen_US
dc.identifier.doihttp://dx.doi.org/10.1016/0045-6535(85)90236-Xen_US
dc.identifier.sourceChemosphereen_US
dc.owningcollnameInterdisciplinary and Peer-Reviewed


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