Literature DB >> 24453019

Elevated CO2 concentration increase the mobility of Cd and Zn in the rhizosphere of hyperaccumulator Sedum alfredii.

Tingqiang Li1, Qi Tao, Chengfeng Liang, Xiaoe Yang.   

Abstract

The effects of elevated CO2 on metal species and mobility in the rhizosphere of hyperaccumulator are not well understood. We report an experiment designed to compare the effects of elevated CO2 on Cd/Zn speciation and mobility in the rhizosphere of hyperaccumulating ecotype (HE) and a non-hyperaccumulating ecotype (NHE) of Sedum alfredii grown under ambient (350 μl l(-1)) or elevated (800 μl l(-1)) CO2 conditions. No difference in solution pH of NHE was observed between ambient and elevated CO2 treatments. For HE, however, elevated CO2 reduced soil solution pH by 0.22 unit, as compared to ambient CO2 conditions. Elevated CO2 increased dissolved organic carbon (DOC) and organic acid levels in soil solution of both ecotypes, but the increase in HE solution was much greater than in NHE solution. After the growth of HE, the concentrations of Cd and Zn in soil solution decreased significantly regardless of CO2 level. The visual MINTEQ speciation model predicted that Cd/Zn-DOM complexes were the dominant species in soil solutions, followed by free Cd(2+) and Zn(2+) species for both ecotypes. However, Cd/Zn-DOM complexes fraction in soil solution of HE was increased by the elevated CO2 treatment (by 8.01 % for Cd and 8.47 % for Zn, respectively). Resin equilibration experiment results indicated that DOM derived from the rhizosphere of HE under elevated CO2 (HE-DOM-E) (90 % for Cd and 73 % for Zn, respectively) showed greater ability to form complexes with Cd and Zn than those under ambient CO2 (HE-DOM-A) (82 % for Cd and 61 % for Zn, respectively) in the undiluted sample. HE-DOM-E showed greater ability to extract Cd and Zn from soil than HE-DOM-A. It was concluded that elevated CO2 could increase the mobility of Cd and Zn due to the enhanced formation of DOM-metal complexes in the rhizosphere of HE S. alfredii.

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Year:  2014        PMID: 24453019     DOI: 10.1007/s11356-014-2560-1

Source DB:  PubMed          Journal:  Environ Sci Pollut Res Int        ISSN: 0944-1344            Impact factor:   4.223


  32 in total

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