scholarly journals Experimental constraints on Li isotope fractionation during the interaction between kaolinite and seawater

2021 ◽  
Vol 292 ◽  
pp. 333-347
Author(s):  
Xu (Yvon) Zhang ◽  
Giuseppe D. Saldi ◽  
Jacques Schott ◽  
Julien Bouchez ◽  
Marie Kuessner ◽  
...  
2019 ◽  
Vol 15 (2) ◽  
pp. 635-646 ◽  
Author(s):  
Holly L. Taylor ◽  
Isaac J. Kell Duivestein ◽  
Juraj Farkas ◽  
Martin Dietzel ◽  
Anthony Dosseto

Abstract. Lithium (Li) isotopes in marine carbonates have considerable potential as a proxy to constrain past changes in silicate weathering fluxes and improve our understanding of Earth's climate. To date the majority of Li isotope studies on marine carbonates have focussed on calcium carbonates. The determination of the Li isotope fractionation between dolomite and a dolomitizing fluid would allow us to extend investigations to deep times (i.e. Precambrian) when dolostones were the most abundant marine carbonate archives. Dolostones often contain a significant proportion of detrital silicate material, which dominates the Li budget; thus, pretreatment needs to be designed so that only the isotope composition of the carbonate-associated Li is measured. This study aims to serve two main goals: (1) to determine the Li isotope fractionation between Ca–Mg carbonates and solution, and (2) to develop a method for leaching the carbonate-associated Li out of dolostone while not affecting the Li contained within the detrital portion of the rock. We synthesized Ca–Mg carbonates at high temperatures (150 to 220 ∘C) and measured the Li isotope composition (δ7Li) of the precipitated solids and their respective reactive solutions. The relationship of the Li isotope fractionation factor with temperature was obtained: 103ln⁡αprec-sol=-(2.56±0.27)106(1)/T2+(5.8±1.3) Competitive nucleation and growth between dolomite and magnesite were observed during the experiments; however, there was no notable effect of their relative proportion on the apparent Li isotope fractionation. We found that Li isotope fractionation between the precipitated solid and solution is higher for Ca–Mg carbonates than for Ca carbonates. If the temperature of a precipitating solution is known or can be estimated independently, the above equation could be used in conjunction with the Li isotope composition of dolostones to derive the composition of the solution and hence make inferences about the past Li cycle. In addition, we also conducted leaching experiments on a Neoproterozoic dolostone and a Holocene coral. Results show that leaching with 0.05 M hydrochloric acid (HCl) or 0.5 % acetic acid (HAc) at room temperature for 60 min releases Li from the carbonate fraction without a significant contribution of Li from the siliciclastic detrital component. These experimental and analytical developments provide a basis for the use of Li isotopes in dolostones as a palaeo-environmental proxy, which will contribute to further advance our understanding of the evolution of Earth's surface environments.


Elements ◽  
2020 ◽  
Vol 16 (4) ◽  
pp. 247-252
Author(s):  
Horst R. Marschall ◽  
Ming Tang

The field of high-temperature Li isotope geochemistry has been rattled by major paradigm changes. The idea that Li isotopes could be used to trace the sources of fluids, rocks, and magmas had to be largely abandoned, because Li diffusion causes its isotopes to fractionate at metamorphic and magmatic temperatures. However, diffusive fractionation of Li isotopes can be used to determine timescales of geologic processes using arrested diffusion profiles. High diffusivity and strong kinetic isotope fractionation favors Li isotopes as a tool to constrain the durations of fast processes in the crust and mantle, where other geochronometers fall short. Time may be the parameter that high-temperature Li isotope studies will be able to shed much light on.


2010 ◽  
Vol 74 (2) ◽  
pp. 241-255 ◽  
Author(s):  
B. M. Shabaga ◽  
M. Fayek ◽  
F. C. Hawthorne

AbstractThe Li and B isotopic compositions of gem-quality Cu-bearing tourmalines were used (1) to distinguish among Paraiba tourmalines from Brazil and Cu-bearing tourmalines from Nigeria and Mozambique; and (2) to identify the likely source of Li and B for these gem-quality tourmalines. The δ11B values of tourmaline from Paraiba, Brazil, range from –42.4‰ to –32.9‰, whereas the δ11B values of Cu-bearing tourmaline from Nigeria and Mozambique range from –30.5‰ to –22.7‰ and –20.8‰ to –19.1‰ respectively. Tourmalines from each locality have relatively homogeneous δ11B values and display no overlap. There is slight overlap between δ7Li values of Paraiba tourmaline (+24.5‰ to +32.9‰) and Cu-bearing tourmaline from Nigeria (+32.4‰ to +35.4‰), and δ7Li values of Cu-bearing tourmaline from Nigeria and Mozambique (+31.5‰ to +46.8‰). Nevertheless, Cu-bearing tourmalines from each locality can be fingerprinted using a combination of their δ11B and δ7Li values. The very small δ11B values are consistent with a non-marine evaporite source, and are among the smallest reported for magmatic systems, expanding the global range of B isotopicc omposition for tourmaline by 12‰. The corresponding large δ7Li values are among the largest reported, although they are less diagnostic of the source of the Li. The large δ7Li values in conjunction with the small δ11B values suggest a non-marine evaporite or brine as a source for Li and B, either as constituent(s) of the magma source region or, by assimilation during magma ascent. The large range in δ11B and δ7Li values suggests that B and Li isotope fractionation occurred during magmatic degassing and late-stage magmatic-hydrothermal evolution of the granite-pegmatite system.


2008 ◽  
Vol 72 (3) ◽  
pp. 780-792 ◽  
Author(s):  
N. Vigier ◽  
A. Decarreau ◽  
R. Millot ◽  
J. Carignan ◽  
S. Petit ◽  
...  

2019 ◽  
Vol 60 (10) ◽  
pp. 1963-1990 ◽  
Author(s):  
Afifé El Korh ◽  
Etienne Deloule ◽  
Béatrice Luais ◽  
Marie-Christine Boiron ◽  
Luc Bastian ◽  
...  

Abstract Ophiolites and high-pressure/low-temperature (HP–LT) terranes are important sites for the study of geochemical cycling in ancient oceanic lithosphere. We have analysed Li abundances and isotope composition in a series of ultrabasic and basic rocks from the Variscan Limousin ophiolite, as well as in basic and pelitic rocks from the Ile de Groix HP–LT terrane. Both bulk and in situ analyses are employed to evaluate Li mobility and isotope fractionation in the oceanic lithosphere during fluid–rock interactions related to seafloor and sub-seafloor hydrothermal alteration, subduction and exhumation processes. In the Limousin ophiolite, early stages of high-temperature (high-T) hydrothermal alteration of oceanic ultrabasic rocks produced serpentine with low Li abundances (0·9–4·6 ppm) and low δ7Li (–8·9‰). The δ7Li increase from –2·2 to +4·2‰ in the following generations of serpentine during late-stage hydrothermal alteration results from changes in the fluid composition and temperature conditions. Therefore, even if dehydrating subducted serpentinites generate high amounts of fluids during subduction, abyssal serpentinites do not constitute an important source of Li for Li-rich metabasic rocks. In the associated amphibolites, hornblende displays typical Li contents (3·1–8·2 ppm) and isotopic compositions (+3·5 to +12·5‰) similar to hydrothermally altered sheeted dykes and gabbros. In contrast, the low Li abundances and extremely high δ7Li values recorded by omphacite and pargasitic amphibole in the ultrahigh-pressure (UHP) zoisite-eclogite from the Limousin probably reflect interaction with a heavy-Li sediment-derived fluid. The HP–LT metabasites of the Ile de Groix record different Li behaviour, with high Li abundances and low δ7Li. They contain Li abundances significantly higher than fresh mid-ocean ridge basalts (MORB) (16–124 ppm), indicating a metasomatic overprint by fluids derived from the neighbouring Li-rich mica-schist (15–52 ppm) in addition to seawater during the early stages of subduction. Lithium is mainly hosted by (1) glaucophane and omphacite in blueschists and eclogites, (2) chlorite and albite in retrograde greenschists, and (3) phengite and chlorite in mica-schists. The metabasites have δ7Li values of –4·8 to +3·2‰ that are generally lower than those of fresh and altered MORB. The intercalated mica-schists display δ7Li values ranging from –1·7 to +0·2‰ that are typical of subducted sediments. The δ7Li decrease from blueschists to eclogites from +1·8 to –4·8‰, as well as the rimward δ7Li decrease in glaucophane from MORB-like δ7Li values to negative values in blueschists (core: –2·4 to +8·8‰; rims: –7·1 to +2·2‰), reveals that significant fluid-induced Li isotope fractionation occurred at the transition from the lawsonite-blueschist facies to the epidote-blueschist facies, and may be triggered by prograde lawsonite breakdown. In eclogites, the low δ7Li measured in whole-rocks (–4·8 to –2·5‰), omphacite (–22·4 to +3·3‰) and glaucophane (–6·9 to +1·4‰) indicates that Li isotope kinetic fractionation had stronger effects under eclogite-facies conditions. The δ7Li increase toward positive values in the most retrogressed greenschist samples suggests Li mineral–fluid isotopic exchange during rehydration reactions and interaction with a Li-heavy fluid that is probably derived from the dehydrating metabasites. Thus, lithium isotope fractionation in the HP–LT rocks of the Ile de Groix highlights migration of heavy-Li fluids along the oceanic crust–mantle interface in the subduction zone.


2019 ◽  
Vol 250 ◽  
pp. 219-237 ◽  
Author(s):  
Ruth S. Hindshaw ◽  
Rebecca Tosca ◽  
Thomas L. Goût ◽  
Ian Farnan ◽  
Nicholas J. Tosca ◽  
...  

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