scholarly journals Stable C, O, and S Isotope Record of Magmatic-Hydrothermal Interactions Between the Falémé Fe Skarn and the Loulo Au Systems in Western Mali

2020 ◽  
Vol 115 (7) ◽  
pp. 1537-1558
Author(s):  
James S. Lambert-Smith ◽  
Andrew Allibone ◽  
Peter J. Treloar ◽  
David M. Lawrence ◽  
Adrian J. Boyce ◽  
...  

Abstract The Gara, Yalea, and Gounkoto Au deposits of the >17 Moz Loulo mining district, largely hosted by the Kofi series metasediments, are located several kilometers to the east of the 650-Mt Fe skarn deposits in the adjacent Falémé batholith. The Au deposits are interpreted to have formed through phase separation of an aqueous-carbonic fluid, which locally mixed with a hypersaline brine of metaevaporite origin. Recognition of an intrusive relationship between the Falémé batholith and Kofi series opens the possibility that the Fe skarns and Au deposits are part of the same mineral system. In this paper, we combine new δ13C, δ18O, and δ34S data from the Karakaene Ndi skarn, Au occurrences along the western margin of the Kofi series, and zircons within plutonic rocks of the Falémé batholith. We combine these with existing data from the Loulo Au deposits to model the contribution of magmatic volatiles to Au mineralization. C and O isotope compositions of auriferous carbonate-quartz-sulfide veins from the Loulo Au deposits have wide ranges (δ13C: –21.7 to –4.5‰ and δ18O: 11.8 to 23.2‰), whereas values from carbonate veins in Kofi series Au prospects close to the Falémé batholith and the Karakaene Ndi Fe skarn deposit have more restricted ranges (δ13C: –16.8 to –3.7‰, δ18O: 11.4 to 17.2‰, and δ13C: –3.0 ± 1‰, δ18O: 12.6 ± 1‰, respectively). Kofi series dolostones have generally higher isotopic values (δ13C: –3.1 to 1.3‰ and δ18O: 19.1 to 23.3‰). Pyrite from Kofi series Au prospects adjacent to the Falémé batholith have a wide range of δ34S values (–4.6 to 14.2‰), similar to pyrite from the Karakaene Ndi skarn (2.8 to 11.9‰), whereas δ34S values of pyrite and arsenopyrite from the Loulo deposits are consistently >6‰. Comparison of the C and O isotope data with water-rock reaction models indicates the Loulo Au deposits formed primarily through unmixing of an aqueous carbonic fluid derived from the devolatilization of sedimentary rocks with an organic carbon component. Isotopic data are permissive of the hypersaline brine that enhanced this phase separation including components derived from both Kofi series evaporite horizons interlayered with the dolostones and a magmatic-hydrothermal brine. This magmatic-hydrothermal component is particularly apparent in O, C, and S isotope data from the Gara deposit and Au prospects immediately adjacent to the Falémé batholith.

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Yuyin Xi ◽  
Ronald S. Lankone ◽  
Li-Piin Sung ◽  
Yun Liu

AbstractBicontinuous porous structures through colloidal assembly realized by non-equilibrium process is crucial to various applications, including water treatment, catalysis and energy storage. However, as non-equilibrium structures are process-dependent, it is very challenging to simultaneously achieve reversibility, reproducibility, scalability, and tunability over material structures and properties. Here, a novel solvent segregation driven gel (SeedGel) is proposed and demonstrated to arrest bicontinuous structures with excellent thermal structural reversibility and reproducibility, tunable domain size, adjustable gel transition temperature, and amazing optical properties. It is achieved by trapping nanoparticles into one of the solvent domains upon the phase separation of the binary solvent. Due to the universality of the solvent driven particle phase separation, SeedGel is thus potentially a generic method for a wide range of colloidal systems.


2021 ◽  
Vol 22 (2) ◽  
pp. 677
Author(s):  
Tausif Altamash ◽  
Wesam Ahmed ◽  
Saad Rasool ◽  
Kabir H. Biswas

Intracellular ionic strength regulates myriad cellular processes that are fundamental to cellular survival and proliferation, including protein activity, aggregation, phase separation, and cell volume. It could be altered by changes in the activity of cellular signaling pathways, such as those that impact the activity of membrane-localized ion channels or by alterations in the microenvironmental osmolarity. Therefore, there is a demand for the development of sensitive tools for real-time monitoring of intracellular ionic strength. Here, we developed a bioluminescence-based intracellular ionic strength sensing strategy using the Nano Luciferase (NanoLuc) protein that has gained tremendous utility due to its high, long-lived bioluminescence output and thermal stability. Biochemical experiments using a recombinantly purified protein showed that NanoLuc bioluminescence is dependent on the ionic strength of the reaction buffer for a wide range of ionic strength conditions. Importantly, the decrease in the NanoLuc activity observed at higher ionic strengths could be reversed by decreasing the ionic strength of the reaction, thus making it suitable for sensing intracellular ionic strength alterations. Finally, we used an mNeonGreen–NanoLuc fusion protein to successfully monitor ionic strength alterations in a ratiometric manner through independent fluorescence and bioluminescence measurements in cell lysates and live cells. We envisage that the biosensing strategy developed here for detecting alterations in intracellular ionic strength will be applicable in a wide range of experiments, including high throughput cellular signaling, ion channel functional genomics, and drug discovery.


Minerals ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 94
Author(s):  
Xiaoxue Tong ◽  
Kaarel Mänd ◽  
Yuhao Li ◽  
Lianchang Zhang ◽  
Zidong Peng ◽  
...  

Banded iron formations (BIFs) are enigmatic chemical sedimentary rocks that chronicle the geochemical and microbial cycling of iron and carbon in the Precambrian. However, the formation pathways of Fe carbonate, namely siderite, remain disputed. Here, we provide photomicrographs, Fe, C and O isotope of siderite, and organic C isotope of the whole rock from the ~2.52 Ga Dagushan BIF in the Anshan area, China, to discuss the origin of siderite. There are small magnetite grains that occur as inclusions within siderite, suggesting a diagenetic origin of the siderite. Moreover, the siderites have a wide range of iron isotope compositions (δ56FeSd) from −0.180‰ to +0.463‰, and a relatively negative C isotope composition (δ13CSd = −6.20‰ to −1.57‰). These results are compatible with the reduction of an Fe(III)-oxyhydroxide precursor to dissolved Fe(II) through microbial dissimilatory iron reduction (DIR) during early diagenesis. Partial reduction of the precursor and possible mixing with seawater Fe(II) could explain the presence of siderite with negative δ56Fe, while sustained reaction of residual Fe(III)-oxyhydroxide could have produced siderite with positive δ56Fe values. Bicarbonate derived from both DIR and seawater may have provided a C source for siderite formation. Our results suggest that microbial respiration played an important role in the formation of siderite in the late Archean Dagushan BIF.


Polymers ◽  
2020 ◽  
Vol 12 (7) ◽  
pp. 1576
Author(s):  
Biswaroop Mukherjee ◽  
Buddhapriya Chakrabarti

Surface segregation of the low molecular weight component of a polymeric mixture is a ubiquitous phenomenon that leads to degradation of industrial formulations. We report a simultaneous phase separation and surface migration phenomena in oligomer–polymer ( O P ) and oligomer–gel ( O G ) systems following a temperature quench that induces demixing of components. We compute equilibrium and time varying migrant (oligomer) density profiles and wetting layer thickness in these systems using coarse grained molecular dynamics (CGMD) and mesoscale hydrodynamics (MH) simulations. Such multiscale methods quantitatively describe the phenomena over a wide range of length and time scales. We show that surface migration in gel–oligomer systems is significantly reduced on account of network elasticity. Furthermore, the phase separation processes are significantly slowed in gels leading to the modification of the well known Lifshitz–Slyozov–Wagner (LSW) law ℓ ( τ ) ∼ τ 1 / 3 . Our work allows for rational design of polymer/gel–oligomer mixtures with predictable surface segregation characteristics that can be compared against experiments.


2021 ◽  
Vol 50 (2-3) ◽  
Author(s):  
Micha Horacek ◽  
Milan Radulovic ◽  
Dejan Jancic ◽  
Stefan Wyhlidal ◽  
Golub Culafic

The potential threat of a landfill projected on a high karst plateau in southwest Montenegro is investigated with respect to the subjacent nearby springs. The locality is called Duboki do. As the springs are used for drinking water supply this investigation is urgently needed. For the springs exist two hypotheses concerning their catchment area: I) from the high karst plateau, or II) from a topographically lower area. The stable H- and O-isotope ratios of water samples from the springs are compared with precipitation isotope data, to reveal the catchment area of the springs. The isotope results indicate that the catchment area of the springs is at higher altitude fitting to, and in good agreement with, winter precipitation from the high karst plateau of the planned land-fill locality.


2017 ◽  
Vol 331 ◽  
pp. 1-15 ◽  
Author(s):  
Raffaella Silvia Iovine ◽  
Fabio Carmine Mazzeo ◽  
Ilenia Arienzo ◽  
Massimo D'Antonio ◽  
Gerhard Wörner ◽  
...  

2021 ◽  
Author(s):  
Jana von Freyberg ◽  
Julia L. A. Knapp ◽  
Andrea Rücker ◽  
Bjørn Studer ◽  
Massimiliano Zappa ◽  
...  

<p>Off-the-shelf portable automatic water samplers, such as the 6712 full-size portable sampler (Teledyne ISCO, Lincoln, USA), are often used in remote locations to collect precipitation or streamwater for subsequent analysis of deuterium and oxygen-18.  The bottles inside these automatic samplers remain open during the full duration of sampler deployment and the collected water samples can thus be subjected to evaporation and vapor exchange.  Both processes are known to alter the isotope composition of the water sample, and thus the questions arise as to 1) how credible the isotope measurements from automatically collected water samples are and 2) how can these isotope effects in the automatic water sampler be reduced?</p><p>We evaluated these questions through laboratory and field experiments in which we quantified the change in isotope composition in the water samples with respect to ambient conditions (air temperature and relative humidity), storage duration, and sample volume.  We found that isotope fractionation in the water samples was substantial under very warm and dry condition, when sample volumes are small or when sample storage exceeded 10 days.  To address these problems, we have designed an evaporation protection method which modifies autosampler bottles using a syringe housing and silicone tube.  We performed paired experiments with open vs. evaporation-protected bottles in Teledyne ISCO 6712 full-size portable samplers to evaluate our design.  We could show that the evaporation protection successfully reduced isotope fractionation in the water samples for storage durations of up to 24 days and for a wide range of ambient conditions; e.g., while deuterium concentrations in the water samples in open bottles changed by ca. 3‰ under very warm and dry conditions, no isotope effect was measured in the bottles equipped with the evaporation protection. Because our design is very cost efficient it can easily be implemented to upgrade Teledyne ISCO’s 6712 full-size portable samplers or other similar devices for collecting more reliable isotope data.</p>


Sign in / Sign up

Export Citation Format

Share Document