Aluminium-organic acid interactions in acid soils: II. Influence of solid phase sorption on organic acid-Al complexation and Al rhizotoxicity
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In: Plant and Soil, Vol. 182, No. 2, 05.1996, p. 229-237.
Research output: Contribution to journal › Article › peer-review
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T1 - Aluminium-organic acid interactions in acid soils
T2 - II. Influence of solid phase sorption on organic acid-Al complexation and Al rhizotoxicity
AU - Jones, Davey L.
AU - Prabowo, Abdul M.
AU - Kochian, L.V.
PY - 1996/5
Y1 - 1996/5
N2 - Malic acid has been implicated as an inducible root mechanism for the detoxification of rhizotoxic Al. The chemical reactions of malate were therefore investigated in four acid soils ranging in pH from 4.30 to 5.00. All the soils behaved similarly, with malate predominantly complexing Al in solution in favor of other metal cations (Fe, Mn, Cu, Zn, Ca and Mg). Comparison of experimental extraction results with theoretical predictions made using Geochem-PC showed a similar agreement, indicating that the behavior of Al and malate in soil was similar to their behavior in an ideal solution. Competitive anion sorption studies with synthetic Fe and Al(OH)3(s) gels showed similar sorption sites for phosphate, citrate and malate, however, malate was weakly sorped in comparison to phosphate and citrate. Sorption was little affected by solution pH. Malate sorption did not appear to be largely influenced by metal complexation in soils; however, sorption onto Fe and Al(OH)3 gels was markedly reduced in the presence of complexing metal cations. The implications of these results in understanding the role of malate exudation from the root in Al detoxification in the rhizosphere are discussed.
AB - Malic acid has been implicated as an inducible root mechanism for the detoxification of rhizotoxic Al. The chemical reactions of malate were therefore investigated in four acid soils ranging in pH from 4.30 to 5.00. All the soils behaved similarly, with malate predominantly complexing Al in solution in favor of other metal cations (Fe, Mn, Cu, Zn, Ca and Mg). Comparison of experimental extraction results with theoretical predictions made using Geochem-PC showed a similar agreement, indicating that the behavior of Al and malate in soil was similar to their behavior in an ideal solution. Competitive anion sorption studies with synthetic Fe and Al(OH)3(s) gels showed similar sorption sites for phosphate, citrate and malate, however, malate was weakly sorped in comparison to phosphate and citrate. Sorption was little affected by solution pH. Malate sorption did not appear to be largely influenced by metal complexation in soils; however, sorption onto Fe and Al(OH)3 gels was markedly reduced in the presence of complexing metal cations. The implications of these results in understanding the role of malate exudation from the root in Al detoxification in the rhizosphere are discussed.
KW - aluminium
KW - chemistry
KW - malate
KW - organic acids
KW - rhizosphere
U2 - 10.1007/BF00029054
DO - 10.1007/BF00029054
M3 - Article
VL - 182
SP - 229
EP - 237
JO - Plant and Soil
JF - Plant and Soil
SN - 0032-079X
IS - 2
ER -