The reconstruction of past volcanism from glaciological archives is based on the measurement of sulfate concentrations in ice. This method does not allow a proper evaluation of the climatic impact of an eruption owing to the uncertainty in classifying an event between stratospheric or tropospheric. This work develops a new method, using anomalous sulfur isotope composition of volcanic sulfate in order to identify stratospheric eruptions over the last millennium. The advantages and limits of this new method are established with the examination of the 10 largest volcanic signals in ice cores from Dome C and South Pole, Antarctica. Of the 10, seven are identified as stratospheric eruptions. Among them, three have been known to be stratospheric (Tambora, Kuwae, the 1259 Unknown Event) and they exhibit anomalous sulfur isotope compositions. Three unknown events (circa 1277, 1230, 1170 A.D.) and the Serua eruption have been identified as stratospheric eruptions, which suggests for the first time that they could have had significant climatic impact. However, the Kuwae and the 1259 Unknown Event stratospheric eruptions exhibit different anomalous sulfur isotope compositions between South Pole and Dome C samples. Differences in sulfate deposition and preservation patterns between the two sites can help explain these discrepancies. This study shows that the presence of an anomalous sulfur isotope composition of volcanic sulfate in ice core indicates a stratospheric eruption, but the absence of such composition does not necessarily lead to the conclusion of a tropospheric process because of differences in the sulfate deposition on the ice sheet.
Sr and Nd isotopic composition of silicate fractions of sediments have been measured in two well dated gravity cores from the eastern Arabian Sea archiving a depositional history of ∼29 and ∼40 ka. The 87Sr/86Sr and ɛNd in the northern core (SS‐3104G; 12.8°N, 71.7°E) ranges from 0.71416 to 0.71840 and −8.8 to −12.8; these variations are limited compared to those in the southeastern core (SS‐3101G; 6.0°N, 74.0°E), in which they vary from 0.71412 to 0.72069 and −9.0 to −15.2 respectively. This suggests that the variation in the relative proportions of sediments supplied from different sources to the core SS‐3104G are limited compared to core SS‐3101G. The 87Sr/86Sr and ɛNd profiles of SS‐3101G exhibit two major excursions, ca. 9 ka and 20 ka, coinciding with periods of Holocene Intensified Monsoon Phase (IMP) and the Last Glacial Maximum (LGM) respectively with more radiogenic 87Sr/86Sr and lower ɛNd during these periods. These excursions have been explained in terms of changes in the erosion patterns in the source regions and surface circulation of the Northern Indian Ocean resulting from monsoon intensity variations. The intensification of North‐East (NE) monsoon and associated strengthening of the East Indian Coastal Current in southwest direction during LGM transported sediments with higher 87Sr/86Sr and lower ɛNd from the western Bay of Bengal to the Arabian Sea. In contrast, enhanced South‐West (SW) monsoon at ∼9 ka facilitated the transport of sediments from the northern Arabian Sea, particularly Indus derived, to the southeastern Arabian Sea. This study thus highlights the impact of monsoon variability on erosion patterns and ocean surface currents on the dispersal of sediments in determining the Sr and Nd isotopic composition of sediments deposited in the eastern Arabian Sea during the last ∼40 ka.
Sulfides from four achondrite meteorite groups are enriched in 33S (up to 0.040 per mil) as compared with primitive chondrites and terrestrial standards. Stellar nucleosynthesis and cosmic ray spallation are ruled out as causes of the anomaly, but photochemical reactions in the early solar nebula could produce the isotopic composition. The large 33S excess present in oldhamite from the Norton County aubrite (0.161 per mil) suggests that refractory sulfide minerals condensed from a nebular gas with an enhanced carbon-oxygen ratio, but otherwise solar composition is the carrier. The presence of a mass-independent sulfur effect in meteorites argues for a similar process that could account for oxygen isotopic anomalies observed in refractory inclusions in primitive chondrites.
Bulk chemical and oxygen, magnesium and silicon isotopic compositions were measured for each of 17 Types A and B refractory inclusions from CV3 chondrites. After bulk chemical compositions were corrected for non-representative sampling in the laboratory, the Mg and Si isotopic compositions of each inclusion were used to calculate its original chemical composition assuming that the heavy-isotope enrichments of these elements are due to Rayleigh fractionation that accompanied their evaporation from CMAS liquids. The resulting pre-evaporation chemical compositions are consistent with those predicted by equilibrium thermodynamic calculations for high-temperature nebular condensates but only if different inclusions condensed from nebular regions that ranged in total pressure from 10 -6 to 10 -1 bar, regardless of whether they formed in a system of solar composition or in one enriched in OC dust relative to gas by a factor of ten relative to solar composition. This is similar to the range of total pressures predicted by dynamic models of the solar nebula for regions whose temperatures are in the range of silicate condensation temperatures. Alternatively, if departure from equilibrium condensation and/or non-representative sampling of condensates in the nebula occurred, the inferred range of total pressure could be smaller. Simple kinetic modeling of evaporation successfully reproduces observed chemical compositions of most inclusions from their inferred pre-evaporation compositions, suggesting that closed-system isotopic exchange processes did not have a significant effect on their isotopic compositions. Comparison of pre-evaporation compositions with observed ones indicates that 80% of the enrichment in refractory CaO + Al 2 O 3 relative to more volatile MgO + SiO 2 is due to initial condensation and 20% due to subsequent evaporation for both Type A and Type B inclusions.
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