Search results for "Carbonate minerals"
showing 10 items of 14 documents
A record of seafloor methane seepage across the last 150 million years
2020
<p>Methane seepage at the seafloor is a source of carbon in the marine environment and has long been recognized as an important window into the deep geo-, hydro-, and bio-spheres. However, the processes and temporal patterns of natural methane emission over multi-million-year time scales are still poorly understood. The microbially-mediated methane oxidation leads to the precipitation of authigenic carbonate minerals within subseafloor sediments, thus providing a potentially extensive record of past methane emission. In this study, we used data on methane-derived authigenic carbonates to build a proxy time series of seafloor methane emission over the last 150 My. We quantitat…
In situ carbon and oxygen isotopes measurements in carbonates by fiber coupled laser diode-induced calcination: A step towards field isotopic charact…
2021
International audience; Natural stable isotopes ratios (δ13Ccarb and δ18Ocarb) of carbonates archived in the geological record are routinely used to reconstruct local and global paleo temperatures and the secular evolution of the biogeochemical carbon cycle. The state-of-the-art technique, employed since the mid 20th century, to measure these isotopic ratios starts with field sampling followed by several steps of physical and chemical laboratory preparation including: (i) microdrilling and/or sawing and crushing, (ii) CO2 release by wet acid digestion, (iii) gas equilibration, purification and transfer, before (iv) gas phase IRMS measurements. While these steps are time and resource consumi…
Sedimentology and isotope geochemistry of Carnian deep-water marl/limestone deposits from the Sicani Mountains, Sicily: Environmental implications an…
1995
Abstract The upper Triassic Halobia-bearing marl/limestone deposits from the Sicani Mountains (Sicily) record the sedimentary evolution of the Sicanian Basin through the middle and late Carnian time. Dark marls and interbedded grey calcilutites of Julian age are characterized by abundant pyrite, sparse bioturbation and negative carbonate carbon δ13C values. They accumulated in a basin with dominantly anoxic to dysaerobic bottom waters. Lower Tuvalian dark-grey pyritic marls and calcilutites, which contain carbonate minerals with relatively high Mn contents and widely fluctuating δ13C signatures, were deposited under dysaerobic conditions. Middle and upper Tuvalian cherty limestones show int…
The influence of natural trace element distribution on the mobility of radionuclides. The exemple of nickel in a clay-rock
2015
International audience; The natural distribution of nickel (Ni) in the Callovian–Oxfordian clay-rich rock of Bure (France) was investigated, together with that of cobalt (Co), zinc (Zn) and lead (Pb). The most Ni-enriched phases are pyrite (∼400 × 10−6 g g−1 Ni), sphalerite (∼300 × 10−6 g g−1), chlorite (∼285 × 10−6 g g−1), organic matter (∼300 × 10−6 g g−1), muscovite (100–200 × 10−6 g g−1) and possibly carbonate minerals (mainly calcite and minor dolomite, ∼10 × 10−6 g g−1). Despite their high abundance (up to ∼80% in the upper part of the formation), carbonate minerals are quantitatively a minor Ni reservoir; most of the Ni is borne by chlorite and pyrite, which are minor mineral phases.…
Zirconium and hafnium fractionation and distribution of Rare Earth Elements in neutral–alkaline waters: Case study of Lake Van hydrothermal system, T…
2021
International audience; We investigated the distribution of Zr, Hf, and rare earth elements (REE) as the sum of lanthanides plus Y in the hydrothermal system in the Lake Van area of south-eastern Turkey. This system is characterised by water with variable pH in alkaline conditions resulting from hydrothermal CO2 upraise and neoformation of calcite minerals in near equilibrium with the interacting waters. Zr, Hf, and REE determinations were carried out for aqueous phases and suspended solids in lake water and surrounding thermal springs. We found that dissolved Hf is partitioned relative to Zr during calcite formation and that such fractionation is a function of the Ca2+ activity in warm wat…
Dissolution and precipitation of gypsum and carbonate minerals in soils on evaporite deposits, central Sicily: isotope geochemistry and microfabric a…
1993
Abstract Soil profiles developed from carbonate- and sulphate-rich deposits of the Gessoso-Solfifera Formation (Miocene) were sampled in central Sicily (544 mm annual precipitation and a strongly seasonal rainfall regime). Carbon and oxygen isotope data supported by mineralogical and thin section investigations indicate that meteoric waters and groundwaters dissolve and repricipitate carbonates and gypsum in the soil profiles. The boundary between the C horizon and the overlying one is the formation site of 18O depleted carbonates (calcite and/or dolomite) presumably precipitated from percolating waters during wet periods. Greater δ18O values of carbonates in the shallower horizons suggest …
The effects of drip rate and geometry on the isotopic composition of speleothems: Evaluation with an advection-diffusion-reaction model
2022
Abstract The curvature and slope of speleothem surfaces have been shown to affect the reaction rates in the aqueous carbonate system by altering the thickness of the CaCO3-precipitating solution. However, the effects of speleothem geometry and drip rate on the speleothem’s carbon and oxygen isotopic composition have yet to be investigated. Over more strongly sloping surfaces, solutions are thinner and flow faster. The effects of thinner and faster-flowing solutions on the isotopic composition of carbonate minerals precipitated from these solutions are of opposite sense. Thinner solutions enhance rates of CO2 degassing and mineral formation, increasing the degree of isotopic distillation of …
Geochemical characteristics of waters in mineralised area of Peloritani Mountains (Sicily, Italy)
2009
Abstract This paper presents the results of a study on the geochemistry of waters circulating in the mineralised area of the south-eastern sector of Mt. Peloritani (north-eastern Sicily, Italy), aimed at basic understanding of the geochemical processes influencing their chemical composition. Chemico-physical parameters and data on 26 major and minor chemical elements are reported for 103 water samples. Water chemistry is mainly dominated by dissolution of carbonates and hydrolysis of aluminosilicate minerals. Total dissolved salts (TDS) range from 80 to 1398 mg/L. All the waters exhibit E H characteristic of an oxygenated environment. Excluding two samples, which show very high H + activity…
Three-dimensional solvation structure of ethanol on carbonate minerals
2020
Calcite and magnesite are important mineral constituents of the earth’s crust. In aqueous environments, these carbonates typically expose their most stable cleavage plane, the (10.4) surface. It is known that these surfaces interact with a large variety of organic molecules, which can result in surface restructuring. This process is decisive for the formation of biominerals. With the development of 3D atomic force microscopy (AFM) it is now possible to image solid–liquid interfaces with unprecedented molecular resolution. However, the majority of 3D AFM studies have been focused on the arrangement of water at carbonate surfaces. Here, we present an analysis of the assembly of ethanol – an o…
Formation of secondary carbonates and native sulphur in sulphate-rich Messinian strata, Sicily
2010
Abstract Microbially formed authigenic carbonates accompanied by native sulphur are present in the ‘Calcare Solfifero’ below a thick succession of gypsum deposited during the Messinian salinity crisis in Sicily. We sampled these carbonates and associated sulphur in five former sulphur mines to subject them to a detailed petrographic and geochemical study in order to explore their different modes of formation. Native sulphur formed in conjunction with microbial sulphate reduction, which is reflected in its depletion in 34S (δ34S values as low as − 2‰ vs. V-CDT) and an enrichment of 34S in the residual sulphate (δ34S values as high as + 61‰). The oxidation of organic matter by sulphate reduct…