4.7 Article

The temperature dependence of feldspar dissolution determined using a coupled weathering-climate model for Holocene-aged loess soils

期刊

GEODERMA
卷 156, 期 1-2, 页码 11-19

出版社

ELSEVIER
DOI: 10.1016/j.geoderma.2009.12.029

关键词

Loess; Feldspar; Weathering kinetics; Climosequence; Activation energy; Global Climate Model

资金

  1. National Science Foundation [CHE-0431329]
  2. Center for Environmental Kinetics Analysis
  3. Bunton-Waller Graduate Award
  4. Charles E. Knopf Scholarship

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Soils developed over the last 10-13 ky on Peoria loess along a transect parallel to the Mississippi River spanning similar to 1600 km from north to south were investigated to estimate the effects of climate on rates of chemical weathering. In the 22 soils, Na concentrations generally decreased from parent composition to the surface, defining depletion profiles that document the weathering of plagioclase. The integrated fraction of Na (f) dissolved from each profile varied from similar to 0 in the north to 26% in the south. This variation is attributed to an increase in average precipitation and temperature from the north (today's average values: 0.5 m/y, 7.5 degrees C) to the south (1.2 m/y, 20.3 degrees C). We used the output from the GENESIS v2 Global Climate Model (GCM) to calculate the mean annual temperature, precipitation, and porefluid advection velocity, v, through the soils for three time points during the last 13,000 y in order to quantify the effect of temperature on Na depletion. To interpret the soils quantitatively, the Na concentration-depth profiles were fit to a sigmoidal model equation that yielded three fit parameters: (i) a lumped kinetic parameter related to the reaction front thickness (K), (ii) the Na concentration in soil at the surface (C-z=0), and (iii) the Na concentration at depth in the parent (C-o). The product Kv, the fraction f, and the concentration difference, C-o-C-z=0, were all observed to vary with temperature along the transect. According to the derivation and assumptions of the sigmoidal model, these values are all functionally related to the dissolution rate constant of albite. The variation in temperature can be explained for Kv and (C-o-C-z=0) based on laboratory values of the activation energy, E-a, for albite dissolution. In contrast, for the case off, the temperature dependence is larger than E-a because it incorporates contributions from both E-a and the reaction enthalpy, Delta H, of albite dissolution. Furthermore, the temperature dependence determined from C-o-C-z=0 yields the best estimate of activation energy for albite dissolution, E-a = 75 +/- 14 kJ/mol, because it is not dependent upon the assumptions of soil texture. Such quantitative interpretations of soil profiles will be useful in predicting the effects of climate on soil chemistry. (C) 2010 Elsevier B.V. All rights reserved.

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