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      Microbial siderophores and root exudates enhanced goethite dissolution and Fe/As uptake by As-hyperaccumulator Pteris vittata

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      Environmental Pollution
      Elsevier BV

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          Abstract

          Arsenic (As) in soils is often adsorbed on Fe-(hydro)oxides surface, rendering them more resistant to dissolution, which is undesirable for phytoremediation of As-contaminated soils. Arsenic hyperaccumulator Pteris vittata prefers to grow in calcareous soils where available Fe and As are low. To elucidate its mechanisms of acquiring Fe and As from insoluble sources in soils, we investigated dissolution of goethite with pre-adsorbed arsenate (AsV; As-goethite) in presence of four organic ligands, including two root exudates (oxalate and phytate, dominant in P. vittata) and two microbial siderophores (PG12-siderophore and desferrioxamine B). Their presence increased As solubilization from As-goethite from 0.03 to 0.27-5.33 mg L-1 compared to the control. The siderophore/phytate bi-ligand treatment released 7.42 mg L-1 soluble Fe, which was 1.2-fold that of the sum of siderophore and phytate, showing a synergy in promoting As-goethite dissolution. In the ligand-mineral-plant system, siderophore/phytate was most effective in releasing As and Fe from As-goethite. Moreover, the continuous plant uptake induced more As-goethite dissolution. The continued release of As and Fe significantly enhanced their plant uptake (from 0.01 to 0.43 mg plant-1 As and 2.7-14.8 mg plant-1 Fe) and plant growth (from 1.2 to 3.1 g plant-1 fw) in P. vittata. Since microbial siderophores and root exudates often coexist in soil rhizosphere, their synergy in enhancing dissolution of insoluble As-Fe minerals may play an important role in efficient phytoremediation of As-contaminated soils.

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          Author and article information

          Journal
          Environmental Pollution
          Environmental Pollution
          Elsevier BV
          02697491
          April 2017
          April 2017
          : 223
          : 230-237
          Article
          10.1016/j.envpol.2017.01.016
          28108165
          c5aae54b-414b-45b0-a3d3-65949c3ab395
          © 2017

          https://www.elsevier.com/tdm/userlicense/1.0/

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