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首页> 外文期刊>Aquatic geochemistry >Application of Gibbs Energy Minimization to Model Early-Diagenetic Solid-Solution Aqueous-Solution Equilibria Involving Authigenic Rhodochrosites in Anoxic Baltic Sea Sediments
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Application of Gibbs Energy Minimization to Model Early-Diagenetic Solid-Solution Aqueous-Solution Equilibria Involving Authigenic Rhodochrosites in Anoxic Baltic Sea Sediments

机译:Gibbs能量最小化在模拟缺氧波罗的海沉积物中自生菱锰矿的早期成岩固溶水-溶液平衡中的应用

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摘要

The natural early-diagenetic environment "anoxic porewater-authigenic mineral phases" has been characterized in sediment of the Gotland Deep. Baltic Sea, by a closed-system model. Occurrence of carbonate precipitates as thin almost pure white laminae was considered as a natural experiment for long-term equilibration between these phases and porewater. Plots of distribution coefficients indicate that metastable equilibrium exists between porewater and the authigenic Ca-rich rhodochrosite phases below 7 cm depth. A thermodynamic model of porewater geochemistry at in situ P = 25 bar and T = 5 ℃ was developed using the Gibbs energy minimization (GEM) approach. The values of isobaric-isothermal potentials of Mn, Ca, Fe, Mg, Sr, Ba, C, and O, calculated from the porewater composition, were used in a new "dual thermodynamic" calculation approach to estimate solid activity coefficients of the end-members in the non-ideal solid solution (Mn, Ca, Mg, Sr, Ba, Fe)CO_3, i.e., at full major and minor multi-component complexity. The regular Margules interaction parameters for the composing binaries estimated by this model were #alpha#_(Mn-Ca) = 1.9 +- 0.5, #alpha#_(Mn-Mg) = 0.6, #alpha#_(Ca-Mg) = 3.7, #alpha#_(Mn-Fe) = 0.2, #alpha#_(Ca-Fe) = 2.8, #alpha#_(Mn-Sr) = 9.7, #alpha#_(Ca-Sr) = 2.15, #alpha#_(Mn-Ba)= 4.0, #alpha#_(Ca-Ba) = 1.4, validating the theoretical predictions given by Lippmann in his pioneering 1980's paper. The strictly thermodynamic equilibrium model is not only able to match both the measured porewater and carbonate solid-solution composition, but also to predict that the porewater pH, pe, alkalinity, and dissolved Mn, Fe, and S concentrations are controlled by the authigenic mineral buffering assemblage mackinawite-greigite-rhodochrosite. Our model is only compatible with the idea of ACR formation with typical composition (X_(Mn) between 70-75%) in the topmost sediment layer which, however, needs a major source of Mn_(aq)~(II). This is provided by reduction of particulate Mn oxides precipitated in significant amounts in the water column upon major inflow events in the Baltic Sea. The model enables also to set up scenarios of changing environmental conditions, e.g., to predict the non-linear response of the carbonate solid-solution composition to changes in Mn loading, alkalinity and salinity of the sediment-water system. The results suggest that the major and especially minor element contents (Sr, Mg, Ba) in authigenic carbonates can be applied as an environmental paleoproxy.
机译:在哥得兰岛深部沉积物中已表征出天然的早期成岩环境“缺氧孔隙-自生矿物相”。波罗的海,采用封闭系统模型。碳酸盐沉淀物的出现是几乎纯白色的薄薄层,被认为是这些相和孔隙水之间长期平衡的自然实验。分布系数图表明,在低于7 cm深度的孔隙水和自生的富含Ca的菱锰矿相之间存在亚稳态平衡。利用吉布斯能量最小化(GEM)方法建立了原位P = 25 bar,T = 5℃的孔隙水地球化学热力学模型。由孔隙水成分计算出的Mn,Ca,Fe,Mg,Sr,Ba,C和O的等压等温势值被用于一种新的“双重热力学”计算方法中,以估算末端的固体活度系数非理想固溶体(Mn,Ca,Mg,Sr,Ba,Fe)CO_3中的碳原子数,即具有完全的主要和次要的多组分复杂度。此模型估算的组成二进制文件的常规Margules相互作用参数为#alpha #_(Mn-Ca)= 1.9 +-0.5,#alpha #_(Mn-Mg)= 0.6,#alpha #_(Ca-Mg) = 3.7,#alpha #_(Mn-Fe)= 0.2,#alpha #_(Ca-Fe)= 2.8,#alpha #_(Mn-Sr)= 9.7,#alpha #_(Ca-Sr)= 2.15 ,#alpha #_(Mn-Ba)= 4.0,#alpha #_(Ca-Ba)= 1.4,验证了Lippmann在其1980年的开创性论文中给出的理论预测。严格的热力学平衡模型不仅能够匹配测得的孔隙水和碳酸盐固溶体成分,而且能够预测孔隙水的pH,pe,碱度以及溶解的Mn,Fe和S浓度受自生矿物的控制。缓冲组合物马氏体-钙铁矿-菱锰矿。我们的模型仅与在最顶层沉积层中具有典型成分(X_(Mn)在70-75%之间)的ACR形成的想法兼容,但是该沉积层需要Mn_(aq)〜(II)的主要来源。这是由于波罗的海发生重大流入事件而减少了在水柱中大量沉淀的颗粒状锰氧化物的提供的。该模型还可以设置变化的环境条件,例如,预测碳酸盐固溶体成分对沉积物-水系统中锰含量,碱度和盐度变化的非线性响应。结果表明,自生碳酸盐中主要和特别是次要元素含量(Sr,Mg,Ba)可以用作环境古过氧化物。

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