Measurement Report: Long-range transport and fate of DMS-oxidation products in the free troposphere derived from observations at the high-altitude research station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes

dc.contributor.authorWiebke Scholz
dc.contributor.authorJiali Shen
dc.contributor.authorDiego Aliaga
dc.contributor.authorCheng Wu
dc.contributor.authorSamara Carbone
dc.contributor.authorIsabel Moreno
dc.contributor.authorQiaozhi Zha
dc.contributor.authorWei Huang
dc.contributor.authorLiine Heikkinen
dc.contributor.authorJean‐Luc Jaffrezo
dc.coverage.spatialBolivia
dc.date.accessioned2026-03-22T20:41:51Z
dc.date.available2026-03-22T20:41:51Z
dc.date.issued2022
dc.descriptionCitaciones: 5
dc.description.abstractAbstract. Dimethyl sulfide (DMS) is the primary natural contributor to the atmospheric sulfur burden. Observations concerning the fate of DMS oxidation products after long-range transport in the remote free troposphere are, however, sparse. Here we present quantitative chemical ionization mass spectrometric measurements of DMS and its oxidation products H2SO4, MSA, DMSO, DMSO2, MSIA, MTF, CH3S(O)2OOH and CH3SOH in the gas-phase as well as measurements of the sulfate and methane- sulfonate aerosol mass fractions at the Global Atmosphere Watch (GAW) station Chacaltaya in the Bolivian Andes located at 5240 m above sea level (a.s.l.). DMS and DMS oxidation products are brought to the Andean high-altitude station by Pacific air masses during the dry season after convective lifting over the remote Pacific ocean to 6000–8000 m a.s.l. and subsequent long-range transport in the free troposphere (FT). Most of the DMS reaching the station is already converted to the rather unreactive sulfur reservoirs dimethyl sulfone (DMSO2) in the gas phase and methanesulfonate (MS−) in the particle phase, which carried nearly equal amounts of sulfur to the station. The particulate sulfate at Chacaltaya is however dominated by regional volcanic emissions during the time of the measurement and not significantly affected by the marine air masses. In one of the FT events, even some DMS was observed next to reactive intermediates such as methyl thioformate, dimethyl sulfoxide, and methane sulfinic acid. Also for this event, backtrajectory calculations show, that the air masses came from above the ocean (distance >330 km) with no local sur- face contacts. This study demonstrates the potential impact of marine DMS emissions on the availability of sulfur-containing vapors in the remote free troposphere far away from the ocean.
dc.identifier.doi10.5194/egusphere-2022-887
dc.identifier.urihttps://doi.org/10.5194/egusphere-2022-887
dc.identifier.urihttps://andeanlibrary.org/handle/123456789/83538
dc.language.isoen
dc.sourceUniversität Innsbruck
dc.subjectDimethyl sulfide
dc.subjectTroposphere
dc.subjectSulfate
dc.subjectDimethylsulfoniopropionate
dc.subjectSulfur cycle
dc.subjectSulfone
dc.subjectSulfur
dc.subjectMethanesulfonic acid
dc.subjectChemistry
dc.subjectEnvironmental chemistry
dc.titleMeasurement Report: Long-range transport and fate of DMS-oxidation products in the free troposphere derived from observations at the high-altitude research station Chacaltaya (5240 m a.s.l.) in the Bolivian Andes
dc.typepreprint

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