Department of Chemistry and Biochemistry, University of California, San Diego, La Jolla, CA 92093;
Research Center for Environmental Changes, Academia Sinica, Taipei 115, Taiwan.
Proc Natl Acad Sci U S A. 2018 Jul 3;115(27):6964-6969. doi: 10.1073/pnas.1801935115. Epub 2018 Jun 18.
Increased anthropogenic-induced aerosol concentrations over the Himalayas and Tibetan Plateau have affected regional climate, accelerated snow/glacier melting, and influenced water supply and quality in Asia. Although sulfate is a predominant chemical component in aerosols and the hydrosphere, the contributions from different sources remain contentious. Here, we report multiple sulfur isotope composition of sedimentary sulfates from a remote freshwater alpine lake near Mount Everest to reconstruct a two-century record of the atmospheric sulfur cycle. The sulfur isotopic anomaly is utilized as a probe for sulfur source apportionment and chemical transformation history. The nineteenth-century record displays a distinct sulfur isotopic signature compared with the twentieth-century record when sulfate concentrations increased. Along with other elemental measurements, the isotopic proxy suggests that the increased trend of sulfate is mainly attributed to enhancements of dust-associated sulfate aerosols and climate-induced weathering/erosion, which overprinted sulfur isotopic anomalies originating from other sources (e.g., sulfates produced in the stratosphere by photolytic oxidation processes and/or emitted from combustion) as observed in most modern tropospheric aerosols. The changes in sulfur cycling reported in this study have implications for better quantification of radiative forcing and snow/glacier melting at this climatically sensitive region and potentially other temperate glacial hydrological systems. Additionally, the unique ΔS-δS pattern in the nineteenth century, a period with extensive global biomass burning, is similar to the Paleoarchean (3.6-3.2 Ga) barite record, potentially providing a deeper insight into sulfur photochemical/thermal reactions and possible volcanic influences on the Earth's earliest sulfur cycle.
喜马拉雅山脉和青藏高原上空人为气溶胶浓度的增加,已经影响了区域气候,加速了冰雪融化,并影响了亚洲的水资源供应和质量。尽管硫酸盐是气溶胶和水圈中的主要化学组成部分,但不同来源的硫酸盐对其的贡献仍存在争议。在这里,我们报告了来自珠穆朗玛峰附近一个偏远淡水高山湖泊的沉积物硫酸盐的多种硫同位素组成,以重建大气硫循环的两个世纪记录。硫同位素异常可用作硫源分配和化学转化历史的探针。与 20 世纪硫酸盐浓度增加的记录相比,19 世纪的记录显示出明显的硫同位素特征。结合其他元素测量结果,同位素示踪剂表明,硫酸盐增加的趋势主要归因于尘埃相关硫酸盐气溶胶的增强和气候引起的风化/侵蚀,这掩盖了源自其他来源的硫同位素异常(例如,平流层中光解氧化过程产生的硫酸盐和/或燃烧排放的硫酸盐),这在大多数现代对流层气溶胶中都有观察到。本研究中报告的硫循环变化,对更好地量化该气候敏感地区的辐射强迫和冰雪融化具有重要意义,并且可能对其他温带冰川水文系统也具有重要意义。此外,19 世纪(广泛的全球生物质燃烧时期)的独特 ΔS-δS 模式与古太古代(36-32 亿年前)重晶石记录相似,这可能为深入了解地球最早的硫循环中的硫光化学/热反应和可能的火山影响提供了更多的信息。