Search results for "δ34S"

showing 9 items of 9 documents

Multiple sulfur and carbon isotope composition of sediments from the Belingwe Greenstone Belt (Zimbabwe): A biogenic methane regulation on mass indep…

2013

Abstract To explore the linkage between mass-independent sulfur isotope fractionation (MIF-S) and δ13Corg excursions during the Neoarchean, as well as the contemporary redox state and biogeochemical cycling of carbon and sulfur, we report the results of a detailed carbon and multiple sulfur (δ34S, δ33S, δ36S) isotopic study of the ∼2.7 Ga Manjeri and ∼2.65 Ga Cheshire formations of the Ngezi Group (Belingwe Greenstone Belt, Zimbabwe). Multiple sulfur isotope data show non-zero Δ33S and Δ36S values for sediments older than 2.4 Ga (i.e. prior to the Great Oxidation Event, GOE), indicating MIF-S thought to be associated with low atmospheric oxygen concentration. However, in several 2.7–2.5 Ga …

Great Oxygenation EventArcheanGeochemistrychemistry.chemical_elementMass-independent fractionationSulfurchemistry.chemical_compoundδ34SIsotope fractionationchemistryGeochemistry and PetrologyIsotopes of carbonSulfateGeologyGeochimica et Cosmochimica Acta
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A 2600-year record of past polycyclic aromatic hydrocarbons (PAHs) deposition at Holzmaar (Eifel, Germany)

2014

Polycyclic aromatic hydrocarbons (PAHs) are a proxy for climate- and human-related historical fire activity which has rarely been used beyond 1800 AD. We explored the concentration and composition patterns of PAHs together with other proxies (charcoal, C, N, S, δ13C, δ15N, and δ34S) in a sediment core of Holzmaar as indicators of variations in climate and anthropogenic activity over the past 2600 years. The concentrations of pyrogenic PAHs remained low (< 500 ng g− 1) from the pre-Roman Iron Age (600 BC) until the first significant increases to ca. 1000–1800 ng g− 1 between 1700 and 1750 AD related to regional iron production. The highest increases in pyrogenic PAH concentrations occurred w…

δ13Cbusiness.industryPaleontologyδ15NOceanographyδ34SIron AgeEnvironmental chemistryvisual_artvisual_art.visual_art_mediumSedimentary organic matterCoalPolycyclic HydrocarbonsbusinessCharcoalEcology Evolution Behavior and SystematicsGeologyEarth-Surface ProcessesPalaeogeography, Palaeoclimatology, Palaeoecology
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Sulfur isotope's signal of nanopyrites enclosed in 2.7 Ga stromatolitic organic remains reveal microbial sulfate reduction.

2018

18 pages; International audience; Microbial sulfate reduction (MSR) is thought to have operated very early on Earth and is often invoked to explain the occurrence of sedimentary sulfides in the rock record. Sedimentary sulfides can also form from sulfides produced abiotically during late diagenesis or metamorphism. As both biotic and abiotic processes contribute to the bulk of sedimentary sulfides, tracing back the original microbial signature from the earliest Earth record is challenging. We present in situ sulfur isotope data from nanopyrites occurring in carbonaceous remains lining the domical shape of stromatolite knobs of the 2.7-Gyr-old Tumbiana Formation (Western Australia). The anal…

ArcheanBiogeochemical cycleGeologic Sediments010504 meteorology & atmospheric sciencesIronGeochemistrychemistry.chemical_elementSulfides010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundδ34S[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/Geochemistry[ SDV.MP ] Life Sciences [q-bio]/Microbiology and ParasitologySulfur IsotopesMicrobial matAnaerobiosisstromatoliteSulfateEcology Evolution Behavior and Systematics0105 earth and related environmental sciencesGeneral Environmental SciencebiologyChemistrySulfatessulfur biogeochemical cycleWestern Australiabiology.organism_classification[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/GeochemistrySulfurDiagenesisTumbiana FormationStromatolite13. Climate actionAnaerobic oxidation of methaneGeneral Earth and Planetary SciencesOxidation-Reductionmicrobial sulfate reduction
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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…

GypsumSettore GEO/02 - Geologia Stratigrafica E Sedimentologica010504 meteorology & atmospheric sciences[SDU.STU.GP]Sciences of the Universe [physics]/Earth Sciences/Geophysics [physics.geo-ph]StratigraphyAlkalinityGeochemistryCarbonate minerals[PHYS.PHYS.PHYS-GEO-PH]Physics [physics]/Physics [physics]/Geophysics [physics.geo-ph]engineering.material010502 geochemistry & geophysics01 natural scienceschemistry.chemical_compoundδ34SMessinian salinity crisiSicilyComputingMilieux_MISCELLANEOUS0105 earth and related environmental sciencesSettore GEO/06 - MineralogiaAnhydriteGeologyAuthigenicSettore GEO/01 - Paleontologia E PaleoecologiaNative sulphurSettore GEO/08 - Geochimica E VulcanologiaDiagenesischemistry13. Climate actionengineeringCarbonateMicrobial sulphate reductionAuthigenic carbonateGeology
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Multi O- and S-isotopes as tracers of black crusts formation under volcanic and non-volcanic atmospheric conditions in Sicily (Italy)

2020

International audience; The deterioration of monument or building stone materials is mostly due to the growth of black crusts that cause blackening and disaggregation of the exposed surface. This study reports on new oxygen (δ17O, δ18O and Δ17O) and sulphur (δ33S, δ34S, δ36S, Δ33S and Δ36S) isotopic analyses of black crust sulphates formed on building stones in Sicily (Southern Italy). The measurements are used to identify the possible influence of volcanic emissions on black crust formation. Black crusts were mostly sampled on carbonate stone substrate in different locations subject to various sulphur emission sources (marine, anthropogenic and volcanic). Unlike atmospheric sulphate aeroso…

Environmental Engineering010504 meteorology & atmospheric sciencesδ18OGeochemistrychemistry.chemical_elementΔ17O anomaly010501 environmental sciences01 natural sciencesIsotopes of oxygenchemistry.chemical_compoundδ34SEnvironmental Chemistryskin and connective tissue diseasesWaste Management and DisposalSettore GEO/09 -Georis. Miner.e Appl.Mineral.-Petrogr. per l'Ambi.ed i B.Cult.0105 earth and related environmental sciences[PHYS.PHYS.PHYS-AO-PH]Physics [physics]/Physics [physics]/Atmospheric and Oceanic Physics [physics.ao-ph]Volcanic emissiongeographygeography.geographical_feature_categoryintegumentary systemfood and beveragesCrustSulphur isotopePollutionSulfurOxygen isotopeDeposition (aerosol physics)chemistryVolcanoBlack crust13. Climate actionCarbonateGeologyStone degradation
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An enormous sulfur isotope excursion indicates marine anoxia during the end-Triassic mass extinction

2020

The role of ocean anoxia as a cause of the end-Triassic marine mass extinction is widely debated. Here, we present carbonate-associated sulfate δ34S data from sections spanning the Late Triassic–Early Jurassic transition, which document synchronous large positive excursions on a global scale occurring in ~50 thousand years. Biogeochemical modeling demonstrates that this S isotope perturbation is best explained by a fivefold increase in global pyrite burial, consistent with large-scale development of marine anoxia on the Panthalassa margin and northwest European shelf. This pyrite burial event coincides with the loss of Triassic taxa seen in the studied sections. Modeling results also indica…

Extinction eventBiogeochemical cycleMultidisciplinaryExtinction010504 meteorology & atmospheric sciencesIsotopefungiengineering.material010502 geochemistry & geophysics01 natural sciencesPerturbation (geology)sulfure isotope end Triassic mass extinctionhumanitieschemistry.chemical_compoundPaleontologyδ34SchemistryengineeringPyriteSulfateGeology0105 earth and related environmental sciences
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Isotopic composition of dissolved sulphate and hydrogen sulphide from some thermal springs of Sicily

1982

Samples of some thermal springs from Sicily have been analysed for the isotopic composition of sulphur-bearing species. The values of δ34S(SO42− (range: +7.3, +31.7‰), δ34S(H2S) (range: −12.2, +27.8), δ34S(S°) (range: +1.9, +24.5) and δ18O(SO42−) (range: −2.5, +23.9) obtained show such a remarkable variability in data as to hypothesize different genetic processes concerning these species. Furthermore, from the available experimental data, the relationship between the isotopic composition of the sulphur in the dissolved sulphate and in the associated hydrogen sulphide (ΔSO42− - H2S = 25 – 30‰) seems to indicate the bacterial reduction of sulphate ion as one of the processes most significantl…

Genetic ProcessesRenewable Energy Sustainability and the EnvironmentChemistryδ18ORange (biology)chemistry.chemical_elementMineralogyGeologyHydrogen sulphideGeotechnical Engineering and Engineering GeologySulfurIsotopic compositionδ34SSulphate IonEnvironmental chemistryGeothermics
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Hydrothermalism in the Tyrrhenian Sea: Inorganic and microbial sulfur cycling as revealed by geochemical and multiple sulfur isotope data

2011

15 pages; International audience; The Palinuro volcanic complex and the Panarea hydrothermal field, both located in the Tyrrhenian Sea (Italy), are associated with island arc magmatism and characterized by polymetallic sulfide mineralization. Dissolved sulfide concentrations, pH, and Eh measured in porewaters at both sites reveal a variable hydrothermal influence on porewater chemistry. Multiple sulfur isotopic measurements for disseminated sulfides (CRS: chromium reducible sulfur) extracted from sediments at Palinuro yielded a broad range in δ34S range between −29.8 and +10.2‰ and Δ33S values between+0.015 and+0.134‰. In contrast, sediments at Panarea exhibit a much smaller range in δ34SCR…

010506 paleontologySulfide[SDE.MCG]Environmental Sciences/Global ChangesGeochemistrychemistry.chemical_elementDisproportionationengineering.material010502 geochemistry & geophysics01 natural sciencesHydrothermal circulationchemistry.chemical_compoundδ34S[SDU.STU.GC]Sciences of the Universe [physics]/Earth Sciences/GeochemistryMassive sulfide complexGeochemistry and PetrologyHydrothermalism14. Life underwaterMultiple sulfur isotopesSulfate0105 earth and related environmental scienceschemistry.chemical_classificationgeographygeography.geographical_feature_categorySulfur cyclingGeology[ SDU.STU.GC ] Sciences of the Universe [physics]/Earth Sciences/GeochemistrySulfur[ SDE.MCG ] Environmental Sciences/Global ChangeschemistryVolcano13. Climate actionengineeringPyriteGeologyChemical Geology
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Tracing the source of gypsum in New Caledonian soils by REE contents and SSr isotopic compositions

1998

Gypsum minerals forming in pedogenic environments in New Caledonia were examined for their S and Sr isotope compositions and REE distributions. Three possible sources were identified: volcanic, soil-derived and marine. However, differentiation based only on the REE contents and normalized patterns was not possible, but, the best preserved volcanic sample yields a negative EuEu∗ anomaly and the lowest GdNYbN ratio due to the high content of organic matter. Mixing calculations of the δ34S values and 87Sr86Sr ratios confirmed that the marine gypsum has a δ34S value close to + 21‰ and an 87Sr86Sr ratio close to 0.70912, and that the volcanic gypsum has a δ34S value of 0‰ and an 87Sr86Sr ratio o…

chemistry.chemical_classificationgeographyGypsumgeography.geographical_feature_categoryGeochemistryMineralogyGeologyFractionationengineering.materialδ34SPedogenesischemistryVolcanoSource rockGeochemistry and PetrologySoil waterengineeringOrganic matterGeologyChemical Geology
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