Time evolution of the mineralogical composition of Mississippi Valley loess over the last 10 kyr: Climate and geochemical modeling

被引:52
作者
Godderis, Yves [1 ]
Williams, Jennifer Z. [2 ]
Schott, Jacques [1 ]
Pollard, Dave [2 ]
Brantley, Susan L. [2 ]
机构
[1] Univ Toulouse, Lab Etud Mecanismes & Transferts Geol, CNRS, Toulouse, France
[2] Penn State Univ, Ctr Environm Kinet Anal, Earth & Environm Syst Inst, University Pk, PA 16802 USA
关键词
SOIL CO2 CONCENTRATIONS; GIBBS FREE-ENERGIES; DISSOLUTION KINETICS; FELDSPAR DISSOLUTION; ALUMINUM SPECIATION; CHEMICAL AFFINITY; CLAY-MINERALS; RATES; PH; TEMPERATURE;
D O I
10.1016/j.gca.2010.08.023
中图分类号
P3 [地球物理学]; P59 [地球化学];
学科分类号
0708 ; 070902 ;
摘要
Anthropogenic and natural climate change affect processes in the atmosphere, biosphere, hydrosphere, and pedosphere. The impact of climate on soil evolution has not been well-explored, largely due to slow rates and the complexity of coupled processes that must be observed and simulated. The rates of mineral weathering in loess deposited 23 kyr ago and experiencing soil formation for 13 kyr are explored here using the WITCH model for weathering and the GENESIS model for climate simulation. The WITCH model, which uses rigorous kinetic parameters and laws with provision for the effect on rates of deviation from equilibrium, can successfully simulate the depletion profiles in the soil for dolomite and albite if soil CO2 is assumed to rise over the last 10 kyr up to about 30-40x the present atmospheric pressure, and if the solubility product of the Ca-smectite is assumed equal to that of an Fe(III)-rich Ca-montmorillonite. Such simulations document that dissolution behavior for silicates and carbonates are strongly coupled through pH, and for Ca-smectite and feldspars through dissolved silica. Such coupling is not incorporated in simple geometric and analytical models describing mineral dissolution, and therefore probably contributes to the long-standing observation of discrepancies among laboratory and field mineral dissolution rates. (C) 2010 Elsevier Ltd. All rights reserved.
引用
收藏
页码:6357 / 6374
页数:18
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