Search results for " petrology"

showing 10 items of 1353 documents

Effects of organic matter complexation on partitioning of transition metals into calcite: Cave-analogue crystal growth experiments

2022

We highlight the potential for first row transition metals to carry paleohydrological signals in speleothems, and argue that these metals constitute valuable proxies for climate reconstructions. Metal availability to speleothems is hypothesised to be restricted by organic complexation, which strongly limits the free ion activity of transition metals (Co2+, Ni2+ and Cu2+) in dripwater, thereby creating a kinetic overprint on metal concentrations and isotope ratios in speleothem calcite. This study presents the results of the first cave-analogue experiments of transition metal partitioning into calcite in the absence and presence of organic ligands. The Geological Microclimate (GeoMic) system…

chemistry.chemical_classificationCalcitegeographyAqueous solutiongeography.geographical_feature_categoryInorganic chemistryNitrilotriacetic acidSpeleothemF800Metalchemistry.chemical_compoundchemistryTransition metalGeochemistry and Petrologyvisual_artvisual_art.visual_art_mediumOrganic matterChelation
researchProduct

Stabilization of polynuclear plutonium(IV) species by humic acid

2014

Abstract Although the formation of tetravalent plutonium (Pu(IV)) polymers with natural organic matter was previously observed by spectroscopy, there is no quantitative evidence of such reaction in batch experiments. In the present study, Pu(IV) interaction with humic acid (HA) was investigated at pH 1.8, 2.5 and 3, as a function of HA concentration and for Pu total concentration equal to 6 × 10−8 M. The finally measured Pu(IV) concentrations ([Pu(IV)]eq) are below Pu(IV) solubility limit. Pu(IV)–HA interaction can be explained by the complexation of Pu(IV) monomers by HA up to [Pu(IV)]eq ∼ 10−8 M. However, the slope of the log–log Pu(IV)–HA binding isotherm changes from ∼0.7 to ∼3.5 for hi…

chemistry.chemical_classificationChemistrychemistry.chemical_elementPlutoniumchemistry.chemical_compoundHydrolysisMonomerTetramerGeochemistry and PetrologyHumic acidSolubilitySpectroscopyStoichiometryNuclear chemistryGeochimica et Cosmochimica Acta
researchProduct

Structurally bound lipids in peat humic acids

2001

Humic acids from highly decomposed peat were subjected to oxidation with alkaline cupric oxide (CuO) at 170°C (single oxidation). Oxidation products were isolated as three fractions, oxidized humic acids, fulvic acids and lipophilic compounds. Isolated oxidized humic acids were subsequently re-oxidized (sequential oxidation) under the same conditions, and released lipophilic compounds were isolated. Lipids released during single and sequential oxidations were determined using capillary gas chromatography and mass spectrometry. Identified compounds accounted for 3.3 and 0.12 wt.% of humic acid content, respectively. Lipid profiles of lipophilic fractions released during single and sequential…

chemistry.chemical_classificationChromatographyOxideFraction (chemistry)Mass spectrometrycomplex mixturesTerpenoidchemistry.chemical_compoundMonomerchemistryGeochemistry and PetrologyOrganic chemistryHumic acidGas chromatographyAbietaneOrganic Geochemistry
researchProduct

Experimental determination of the phase relations of Pt and Pd antimonides and bismuthinides in the Fe-Ni-Cu sulfide systems between 1100 and 700 °C

2020

Abstract The stability relations of Pt and Pd antimonides and bismuthinides in the Sb- and Bi-bearing Fe-Ni-Cu sulfide systems have been experimentally determined at temperatures between 1100 and 700 °C in evacuated silica tubes. Both PtSb and PdSb are stable as immiscible liquids at temperatures above 1100 and 1000 °C, respectively. The Fe-Ni-Cu-sulfide melt that coexists with the immiscible antimonide melt can dissolve up to 3.8 wt% Sb at 1100 °C, whereas monosulfide solid solution (mss) dissolves very low amounts of Sb over the entire 1100–700 °C temperature range. The liquidus of Pt-antimonides and Pdantimonides are above 980 and 750 °C, respectively. Bismuth does not form immiscible me…

chemistry.chemical_classificationGeophysicsMaterials science010504 meteorology & atmospheric sciencesSulfidechemistryGeochemistry and PetrologyPhase (matter)Analytical chemistry010502 geochemistry & geophysics01 natural sciences0105 earth and related environmental sciencesAmerican Mineralogist
researchProduct

Determination of volatile fatty acids in the hot springs of Vulcano, Aeolian Islands, Italy

1998

Abstract Samples of relatively acid hydrothermal fluids were collected in the spring of 1996 from seeps, springs, and wells on the Island of Vulcano in the southern Tyrrhenian Sea and analyzed for volatile fatty acids 1 using liquid chromatography. Concentrations of VFAs in the seeps were in the range 65–140 ppb formic, 133–184 ppb acetic, and

chemistry.chemical_classificationHot springgeographygeography.geographical_feature_categoryCarboxylic acidMineralogyHydrothermal circulationVolatile fatty acidsMediterranean seachemistryGeochemistry and PetrologyEnvironmental chemistrySpring (hydrology)Environmental scienceAeolian processesWest mediterraneanOrganic Geochemistry
researchProduct

Thallium geochemistry in the metamorphic Lengenbach sulfide deposit, Switzerland: Thallium-isotope fractionation in a sulfide melt

2014

The Lengenbach (Switzerland) Pb-As-Tl-Zn deposit was formed from a sulfide melt at about 500 °C during Alpine metamorphism, but details on its formation and especially the source of the metals are still under debate. In this study we present two sample sets to address these questions: 1. MC-ICP-MS analyses of thallium isotopes in sulfides, sulfosalts, and melt inclusions from the Alpine metamorphic Lengenbach deposit in the Binn Valley of Switzerland, the non-metamorphic Wiesloch Mississippi Valley-type deposit in Southern Germany, and the Cu- and As-rich mineralization at Pizzo Cervandone about 2 km SW of the Lengenbach deposit, which has been discussed as potential source of the Lengenbac…

chemistry.chemical_classificationMineralization (geology)SulfideMetamorphic rockCountry rockGeochemistryMineralogyMetamorphismGeophysicsIsotope fractionationchemistryGeochemistry and PetrologyGeologyGneissMelt inclusionsAmerican Mineralogist
researchProduct

Photoautotrophic community changes in Lagunillo del Tejo (Spain) in response to lake level fluctuation: Two centuries of sedimentary pigment records

2009

Lagunillo del Tejo is a small doline lake in a karstic region of the Iberian Ranges (central-eastern Spain) that undergoes significant lake level fluctuation in response to changing aquifer influxes. In order to assess changes in the primary producer community in the lake over the last two centuries and to elucidate whether these were conditioned by climatic variability, photosynthetic pigments and their derivatives were extracted from the sediments and the data analysed using multivariate statistical techniques. Quantitative variations in total pigment concentrations through the sedimentary sequence are considered a result of changes in sedimentation rate, largely due to lake level fluctua…

chemistry.chemical_classificationOceanographyPrimary producerschemistryGeochemistry and PetrologyLittoral zoneEnvironmental scienceSedimentOrganic matterPlanktonSedimentationBioindicatorMacrophyteOrganic Geochemistry
researchProduct

Chemical evolution of ore-forming brines – Basement leaching, metal provenance, and the redox link between barren and ore-bearing hydrothermal veins.…

2019

Abstract Six mineralogically exemplary barren and mineralized hydrothermal veins (with Pb and Zn ores) of Jurassic-Cretaceous and Cenozoic age in the Schwarzwald mining district, SW Germany were chosen to shed light on the origin of their mineralogical diversity. The selection of the veins was guided by the fact that they represent the largest number of veins in the region, are very well known mineralogically and geochemically, and they provide nice examples of barren and mineralized veins of similar age. Fluid inclusion data from the individual veins overlap implying their diverse mineralogy is not caused by different fluid compositions participating during fluid mixing. LA-ICPMS data of s…

chemistry.chemical_classificationProvenanceMineralization (geology)010504 meteorology & atmospheric sciencesSulfideGeochemistryTrace elementGeology010502 geochemistry & geophysics01 natural sciencesHydrothermal circulationchemistryGeochemistry and PetrologyFluid inclusionsClay mineralsBase metalGeology0105 earth and related environmental sciencesChemical Geology
researchProduct

Effect of ramp size and sample spinning speed on CPMAS 13C NMR spectra of soil organic matter

2011

Abstract Cross polarization (CP) magic angle spinning (MAS) 13C NMR spectroscopy is a solid state NMR technique widely applied to study the chemical composition of natural organic matter. In high magnetic fields (>7 T), fast sample spinning is required in order to reduce the influence of spinning sidebands underlying other chemical shift regions. As the spinning speed increases, the Hartmann–Hahn matching profiles break down into a series of narrow matching bands. In order to account for this instability variable amplitude cross polarization techniques (e.g. VACP, ramp-CP) have been developed. In the present study, we experimentally verified the stability of the Hartmann–Hahn condition unde…

chemistry.chemical_classificationSettore AGR/13 - Chimica AgrariaAnalytical chemistryCarbon-13 NMRSpectral lineMagnetic fieldAmplitudeSolid-state nuclear magnetic resonancechemistryGeochemistry and Petrologysoil organic matterCPMAS 13C NMRMagic angle spinningHumic acidSpinningOrganic Geochemistry
researchProduct

Temporal fatty acid profiles of human decomposition fluid in soil

2017

Abstract We studied the changes in concentration and relative abundance of human-derived fatty acids (FAs) in soil over a period of one year. The study is based on analysis of soil underneath a human body that lay on the soil surface for 18 days before it was discovered. Soil samples were taken when the body was removed, and also 358 days later. Large amounts of the total FA concentration at the start of the measurement period were still present one year after the removal of the body. The FA profile suggested that extensive saturated FA reduction occurred during the first 18 days after deposition. 10-Hydroxystearic acid and FA salts, which are characteristic of adipocere, were abundant in a…

chemistry.chemical_classificationSoil test010401 analytical chemistryMyristic acidFatty acidAdipocere01 natural sciencesDecomposition0104 chemical sciences03 medical and health scienceschemistry.chemical_compound0302 clinical medicineDeposition (aerosol physics)chemistryGeochemistry and PetrologyEnvironmental chemistry030216 legal & forensic medicineGas chromatography–mass spectrometryRelative species abundanceOrganic Geochemistry
researchProduct