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首页> 外文期刊>American Journal of Science >REPLY TO COMMENT BY ROBERT A. BERNER ON 'EFFECT ECT OF ORGANIC LIGANDS AND HETEROTROPHIC BACTERIA ON WOLLASTONITE DISSOLUTION KINETICS',AMERICAN JOURNAL OF SCIENCE,V. 309, P. 731-772
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REPLY TO COMMENT BY ROBERT A. BERNER ON 'EFFECT ECT OF ORGANIC LIGANDS AND HETEROTROPHIC BACTERIA ON WOLLASTONITE DISSOLUTION KINETICS',AMERICAN JOURNAL OF SCIENCE,V. 309, P. 731-772

机译:答复罗伯特·A·伯纳关于“有机液体和异养细菌对硅灰石溶解动力学的影响”的评论。 309,第731-772页

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摘要

R. A. Berner is right saying that the last statement of our paper should have been clarified to apply only to non-aluminous basic silicates. Indeed, by "basic, Ca-Mg bearing silicates" we mean pyroxenes, olivines and pyroxenoids. We also agree that Fe release from olivine and pyroxenes is influenced by the presence of organic acids and chelators as also demonstrated by works on Fe and trace element mobilization from basalt (Hausrath and others, 2009). We further agree with R. A. Berner that the use of wollastonite as an example for the weathering of most basic igneous rocks is misleading for a number of reasons. First, wollastonite forms much thicker Si-rich, Ca-depleted layers, compared to other Ca, Mg-bearings silicates; this altered layer may control overall reactivity of the mineral (Schott and others, 2009). Secondly, alumosilciate minerals, which dominate many weathering systems are likely to be more affected by thepresence of soil biota because organic ligands may decrease the aqueous activity of Al~3+ thus: i) increasing the chemical affinity of the dissolving phase and ii) increasing the solubility of secondary phases so more dissolved constituents remain in solution and move to the ocean (Oelkers and Schott, 1998).
机译:R. A. Berner说的没错,我们的文件的最后声明应该已经澄清,仅适用于无铝碱性硅酸盐。实际上,“含Ca-Mg的碱性硅酸盐”是指辉石,橄榄石和辉石类化合物。我们还同意,橄榄石和辉石中的铁释放受有机酸和螯合剂的存在的影响,铁和玄武岩中微量元素的动员也证明了这一点(Hausrath等人,2009)。我们进一步同意R. A. Berner的观点,使用硅灰石作为大多数基本火成岩风化的例子有许多误导性。首先,与其他含钙,镁的硅酸盐相比,硅灰石形成的硅富集,贫钙层要厚得多。这种改变的层可以控制矿物的整体反应性(Schott等,2009)。其次,在许多风化系统中占主导地位的铝硅酸盐矿物可能更受土壤生物区系的影响,因为有机配体可能会降低Al〜3 +的水活度,因此:i)增加溶解相的化学亲和力; ii)增加第二相的溶解度,使更多溶解的成分保留在溶液中并移至海洋(Oelkers和Schott,1998年)。

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