scholarly journals Silicon Isotope Geochemistry: Fractionation Linked to Silicon Complexations and Its Geological Applications

Molecules ◽  
2019 ◽  
Vol 24 (7) ◽  
pp. 1415 ◽  
Author(s):  
Wang ◽  
Wei ◽  
Jiang ◽  
Liu ◽  
Lei ◽  
...  

The fundamental advances in silicon isotope geochemistry have been systematically demonstrated in this work. Firstly, the continuous modifications in analytical approaches and the silicon isotope variations in major reservoirs and geological processes have been briefly introduced. Secondly, the silicon isotope fractionation linked to silicon complexation/coordination and thermodynamic conditions have been extensively stressed, including silicate minerals with variable structures and chemical compositions, silica precipitation and diagenesis, chemical weathering of crustal surface silicate rocks, biological uptake, global oceanic Si cycle, etc. Finally, the relevant geological implications for meteorites and planetary core formation, ore deposits formation, hydrothermal fluids activities, and silicon cycling in hydrosphere have been summarized. Compared to the thermodynamic isotope fractionation of silicon associated with high-temperature processes, that in low-temperature geological processes is much more significant (e.g., chemical weathering, biogenic/non-biogenic precipitation, biological uptake, adsorption, etc.). The equilibrium silicon isotope fractionation during the mantle-core differentiation resulted in the observed heavy isotope composition of the bulk silicate Earth (BSE). The equilibrium fractionation of silicon isotopes among silicate minerals are sensitive to the Si–O bond length, Si coordination numbers (CN), the polymerization degrees of silicate unites, and the electronegativity of cations in minerals. The preferential enrichment of different speciation of dissoluble Si (DSi) (e.g., silicic acid H4SiO40 (H4) and H3SiO4− (H3)) in silica precipitation and diagenesis, and chemical weathering, lead to predominately positive Si isotope signatures in continental surface waters, in which the dynamic fractionation of silicon isotope could be well described by the Rayleigh fractionation model. The role of complexation in biological fractionations of silicon isotopes is more complicated, likely involving several enzymatic processes and active transport proteins. The integrated understanding greatly strengthens the potential of δ30Si proxy for reconstructing the paleo terrestrial and oceanic environments, and exploring the meteorites and planetary core formation, as well as constraining ore deposits and hydrothermal fluid activity.

2010 ◽  
Vol 295 (3-4) ◽  
pp. 487-496 ◽  
Author(s):  
Karen Ziegler ◽  
Edward D. Young ◽  
Edwin A. Schauble ◽  
John T. Wasson

2014 ◽  
Vol 142 ◽  
pp. 95-114 ◽  
Author(s):  
Sonja Geilert ◽  
Pieter Z. Vroon ◽  
Desiree L. Roerdink ◽  
Philippe Van Cappellen ◽  
Manfred J. van Bergen

2015 ◽  
Vol 164 ◽  
pp. 403-427 ◽  
Author(s):  
Sonja Geilert ◽  
Pieter Z. Vroon ◽  
Nicole S. Keller ◽  
Snorri Gudbrandsson ◽  
Andri Stefánsson ◽  
...  

1991 ◽  
Vol 55 (380) ◽  
pp. 303-315 ◽  
Author(s):  
Paul B. Barton

AbstractOver the past several decades, thinking about chemical processes in rocks had been dominated by experimental and theoretical treatments of mineral equilibrium, which is the state from which the time variable has been excluded. But, to an extent exceeding that of any of our sister sciences, we in geology are concerned with the behaviour of things as a function of time; thus equilibrium is but one of several interesting boundary conditions. Textures, (defined as the spatial relations within and among minerals and fluids, regardless of scale or origin) provide a means to sort out and identify successive states. In fact, it is the pattern of evolution of those states that enables us to deduce the processes. We may well draw the analogy with thermodynamics and kinetics, respectively:equilibrium textures and phase assemblages, via thermodynamic analysis → definition of conditions of equilibration,whereaskinetics, as displayed in disequilibrium textures → sequence of events and processes of mineralization.The interpretation of textures is one of the most difficult yet important aspects of the study of rocks and ores, and there are few areas of scientific endeavour that are more subject to misinterpretation. Although the difficulties are many, the opportunites for new understanding are also abundant. Textural interpretations have many facets: some are well established and accepted; some that are accepted may be wrong; others are recognised to be speculative and controversial; and we trust that still other textural features remain to be described and interpreted. This paper will deal principally with low-temperature, epigenetic ore deposits, and will emphasise silica and sphalerite; but extension to other materials is not unreasonable.Ore and gangue minerals react internally, or with their environment, at widely ranging rates, ranging from the almost inert pyrite, arsenopyrite, well-crystallised quartz, and tourmaline to the notoriously fickle copper/iron and copper/silver sulfides. Arrested or incomplete reactions may be identifed by textural criteria and, when appropriately quantified, can provide guides to the duration of geological processes.In recent years so much emphasis has been placed on isotopes, fluids, chemistry, and deposit and process models that the textural features have been ignored. In part this oversight occurs because we have grown accustomed to using superposition, cross-cutting, pseudomorphism, mutual intergrowths, exsolution and so on as off-the-shelf tools, to be grasped and applied without evaluation or even description. Surely science must build on previous work without constant and exhaustive reassessment, but for mineral textures a little reassessment may yield substantial benefit.


Elements ◽  
2020 ◽  
Vol 16 (6) ◽  
pp. 401-406 ◽  
Author(s):  
Andreas Audétat ◽  
Marie Edmonds

Magmatic-hydrothermal fluids play a key role in a variety of geological processes, including volcanic eruptions and the formation of ore deposits whose metal content is derived from magmas and transported to the site of ore deposition by means of hydrothermal fluids. Here, we explain the causes and consequences of fluid saturation in magmas, the corresponding fluid-phase equilibria, and the behavior of metals and ligands during the transition from magma to an exsolved hydrothermal fluid. Much of what we know about magmatic-hydrothermal systems stems from the study of fluid inclusions, which are minute droplets of fluids trapped within minerals during mineral growth.


Langmuir ◽  
2016 ◽  
Vol 32 (35) ◽  
pp. 8872-8881 ◽  
Author(s):  
Wei Wang ◽  
Hai-Zhen Wei ◽  
Shao-Yong Jiang ◽  
Christopher J. Eastoe ◽  
Qi Guo ◽  
...  

Author(s):  
F. LELONG ◽  
Y. TARDY ◽  
G. GRANDIN ◽  
J.J. TRESCASES ◽  
B. BOULANGE

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