An international intercomparison of stable carbon isotope composition measurements of dissolved inorganic carbon in seawater

We report results of an intercomparison of stable carbon isotope ratio measurements in seawater dissolved inorganic carbon (δ 13C‐DIC) which involved 16 participating laboratories from various parts of the world. The intercomparison involved distribution of samples of a Certified Reference Material for seawater DIC concentration and alkalinity and a preserved sample of deep seawater collected at 4000 m in the northeastern Atlantic Ocean. The between‐lab standard deviation of reported uncorrected values measured with diverse analytical, detection, and calibration methods was 0.11‰ (1σ ). The multi‐lab average δ 13C‐DIC value reported for the deep seawater sample was consistent within 0.1‰ with historical measured values for the same water mass. Application of a correction procedure based on a consensus value for the distributed reference material, improved the between‐lab standard deviation to 0.06‰. The magnitude of the corrections were similar to those used to correct independent data sets using crossover comparisons, where deep water analyses from different cruises are compared at nearby locations. Our results demonstrate that the accuracy/uncertainty target proposed by the Global Ocean Observing System (±0.05‰) is attainable, but only if an aqueous phase reference material for δ 13C‐DIC is made available and used by the measurement community. Our results imply that existing Certified Reference Materials used for seawater DIC and alkalinity quality control are suitable for this purpose, if a “Certified” or internally consistent “consensus” value for δ 13C‐DIC can be assigned to various batches.publishedVersio

Isotopic composition of mud-volcanic waters from the Taman Peninsula (Russia) and from Kakheti (Eastern Georgia)

d18O and dD values in mud-volcanic waters of the Taman Peninsula and Kakheti vary from +0.7 to +10.0 per mil and from -37 to -13 per mil, respectively. These values increase as the Greater Caucasus is approached. Increase in d18O and dD also positively correlates with fluid generation temperatures based on hydrochemical geothermometers. This is accompanied by changes in chemical composition of waters, in which concentrations of alkali metals, HCO3- ion, and boron increase, while concentrations of halogen ions (Cl-, Br-, J-) decrease. Changes in isotopic composition of water are also accompanied by increase of d13C in methane and decrease of d11B in clays. Analysis of formal models of evolution of isotopic composition of mud-volcanic waters shows that mud volcanoes are recharged by freshened water from the Maikop paleobasin with inferred isotopic composition of dD~-40 per mil and d18O~-6 per mil. Based on this assumption, d18O and dD values observed in mud-volcanic waters can be explained not only by processes of distillation and condensation in a closed system, but also by combined processes of isotopic re-equilibration in the water-illite-methane system

δD, δ¹⁸O concentrations in water samples of the Laptev Sea from cruise AMK63 and AMK69 in 2015

Oxygen and hydrogen isotope data were obtained in water samples collected in the Laptev Sea along the 130.5E meridian in route 63 of R/V "Akademik Mstislav Keldysh" in 2015 and in route 69 of R/V "Akademik Mstislav Keldysh" in 2017. Sampling was done using the Rosette SBE 32. Isotope analysis was performed in the laboratory of Isotope Geochemistry and Geochronology of IGEM RAS (Moscow) in 2015-2016 (for route 63) and in 2017 (for route 69). Oxygen isotope composition of water samples determined by CF IRMS using the Delta V+ with the GasbenchII option (Thermo, Germany). Hydrogen isotope composition of water samples determined by DI IRMS using the DeltaPlus with H/Device option (Thermo, Germany). The δD and δ¹⁸O values were determined with an accuracy of 0.3 and 0.05 per mill correspondently

Chemical and isotope compositions of thermal and surficial waters from the Chukotka Peninsula

Twenty three groups of thermomineral springs in the eastern Chukotka with discharge temperature from 2 to 97°C and mineralization from 1.47 to 37.14 g/l are studied and compared with surface freshwater from their localities. dD and d18O values in surface waters vary from -121.4 to -89.5 per mil and from -16.4 to -11.1 per mil, respectively, while respective values in thermomineral waters range from -134.2 to -92.5 per mil and from -17.6 to -10.5 per mil. dD value in surface waters decreases from the east to the west, i.e. toward interior areas of the peninsula. Hydrothermal springs most depleted in deuterium (dD < -120 per mil) are localized in the geodynamically active Kolyuchinskaya-Mechigmen Depression. According to the proposed formation model of Chukotka thermomineral waters their observed chemical and isotopic characteristics could result from mixing (in different proportions) of surface waters with the deep-sourced isotopically light mineralized component (dD = ca. -138 per mil, d18O = ca. -19 per mil, ? = from 9.5 to 14.7 g/l). The latter originates most likely from subpermafrost waters subjected to slight cryogenic metamorphism

Mineralogy and Geochemistry of Ocelli in the Damtjernite Dykes and Sills, Chadobets Uplift, Siberian Craton: Evidence of the Fluid–Lamprophyric Magma Interaction

The study reports petrography, mineralogy and carbonate geochemistry and stable isotopy of various types of ocelli (silicate-carbonate globules) observed in the lamprophyres from the Chadobets Uplift, southwestern Siberian craton. The Chadobets lamprophyres are related to the REE-bearing Chuktukon carbonatites. On the basis of their morphology, mineralogy and relation with the surrounding groundmass, we distinguish three types of ocelli: carbonate-silicate, containing carbonate, scapolite, sodalite, potassium feldspar, albite, apatite and minor quartz ocelli (K-Na-CSO); carbonate–silicate ocelli, containing natrolite and sodalite (Na-CSO); and silicate-carbonate, containing potassium feldspar and phlogopite (K-SCO). The K-Na-CSO present in the most evolved damtjernite with irregular and polygonal patches was distributed within the groundmass; the patches consist of minerals identical to minerals in ocelli. Carbonate in the K-Na-CSO are calcite, Fe-dolomite and ankerite with high Sr concentration and igneous-type REE patterns. The Na-CSO present in Na-rich damtjernite with geochemical signature indicates the loss of the carbonate component. Carbonate phases are calcite and Fe-dolomite, and they depleted in LREE. The K-SCO was present in the K-rich least-evolved damtjernite. Calcite in the K-SCO has the highest Ba and the lowest Sr concentration and U-shaped REE pattern. The textural, mineralogical and geochemical features of the ocelli and their host rock can be interpreted as follows: (i) the K-Na-CSO are droplets of an alkali–carbonate melt that separated from residual alkali and carbonate-rich melt in highly evolved damtjernite; (ii) the Na-CSO are droplets of late magmatic fluid that once exsolved from a melt and then began to dissolve; (iii) the K-SCO are bubbles of K-P-CO2 fluid liberated from an almost-crystallised magma during the magmatic–hydrothermal stage. The geochemical signature of the K-SCO carbonate shows that the late fluid could leach REE from the host lamprophyre and provide for REE mobility

Petrogenesis of ultramafic rocks of komatiitic composition from the Central Zone of the Limpopo Belt, South Africa: Evidence from O and H isotopes

Komatiites are MgO-rich ultramafic volcanic rocks, mostly interpreted to be essentially anhydrous at the time of extrusion, and are often characterized by spinifex texture. They mainly occur in Archean or Proterozoic greenstone belts within cratons. However, in the Central Zone of the Limpopo Belt in South Africa, ultramafic rocks of komatiitic composition occur within a high-grade metamorphic terrane. Their chemical composition overlaps with that of Al-undepleted (Munro-type) komatiites from elsewhere, but unlike komatiites, they are mainly composed of pargasitic amphibole, along with olivine, orthopyroxene, Cr-rich spinel and magnetite. The studied rocks have a narrow range of whole rock δ18O values (+5.4 to +6.3‰), unlike δ18O values from komatiites, which are generally altered and have δ18O values from ∼+2 to +9‰. However, they are within the range estimated for unaltered komatiites (+5.4 to +6.0‰). Amphibole separates from the studied rocks have δ18O values between +5.5 and + 6.1‰, similar to that of the bulk rock. The δD values of amphiboles range between −78 and −83‰, similar to primary amphiboles from other komatiites and many other mantle-derived mafic igneous rocks. The δ18O values, along with textural and mineralogical evidence, are consistent with the ultramafic rocks of komatiitic composition from the Limpopo Belt being intrusive and unaffected by low-temperature alteration. The O and H isotope composition of the amphiboles are consistent with them being primary magmatic in origin. It cannot be distinguished with certainty whether the water was introduced to the magma through partial melting of hydrated mantle or during ascent through hydrous mantle subsequent to their formation. The minerals observed at present most likely crystallized from komatiite magma that intruded into the lower crust and subsequently re-equilibrated at the ambient P-T conditions