1987
DOI: 10.1016/0016-7037(87)90072-x
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Rare earth element complexation by carbonate and oxalate ions

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Cited by 454 publications
(197 citation statements)
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“…Although the REE are quantitatively transferred from the source to the sediment (e.g., McLennan et al, 1993), intense weathering produces LREE/HREE fractionation (e.g., Mongelli, 1998), possibly due to preferential HREE retention in solution (e.g., Cantrell and Byrne, 1987). For instance carbonate complexes show an increase in stability with increasing atomic number and a preferential retention of HREE in solution as carbonate ions may cause an increase in the (La/Yb) ch and slight alkaline conditions may also favour a preferential LREE retention via adsorption onto particle surfaces (Sholkovitz, 1995).…”
Section: Source-area Weatheringmentioning
confidence: 99%
“…Although the REE are quantitatively transferred from the source to the sediment (e.g., McLennan et al, 1993), intense weathering produces LREE/HREE fractionation (e.g., Mongelli, 1998), possibly due to preferential HREE retention in solution (e.g., Cantrell and Byrne, 1987). For instance carbonate complexes show an increase in stability with increasing atomic number and a preferential retention of HREE in solution as carbonate ions may cause an increase in the (La/Yb) ch and slight alkaline conditions may also favour a preferential LREE retention via adsorption onto particle surfaces (Sholkovitz, 1995).…”
Section: Source-area Weatheringmentioning
confidence: 99%
“…In the marine environment, La is known as the most reactive element of the trivalent REEs (Cantrell and Byrne, 1987;Sholkovitz et al, 1994;Lerche and Nozaki, 1998). An average La concentration in 0-1000 m depth in the North Pacific was reported to be 20 pmol/kg (Zhang et al, 1994).…”
Section: Sc Th and Rees As Indicators Of The Origin Of Aluminosilicatesmentioning
confidence: 99%
“…The literature abounds with studies on REE fractionation due to bindings to different common ligands such as carbonates, sulphates, phosphates, acetates, oxalates, etc. The readers may be referred to the works of Evans [36], Cantrell and Byrne [37], Millero [38], Tao et al [39], among many others. The enrichment in LREEs in the plants studied here can be explained as resulting from high concentrations of low-molecular organic ligands, such as citrates, malates and oxalates, in the rhizosphere solutions [40][41][42], whereas the enrichment in HREEs could result from their complexation with intrinsic chelators in the xylem.…”
Section: The Ree Contents and Distributionmentioning
confidence: 99%