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Abstract. Tidal salt marsh soils can be a dynamic source of greenhouse gases such ascarbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O),as well as sulfur-based trace gases such as carbon disulfide (CS2) anddimethylsulfide (DMS) which play roles in global climate and carbon–sulfurbiogeochemistry. Due to the difficulty in measuring trace gases in coastalecosystems (e.g., flooding, salinity), our current understanding is based onsnapshot instantaneous measurements (e.g., performed during daytime lowtide) which complicates our ability to assess the role of these ecosystemsfor natural climate solutions. We performed continuous, automatedmeasurements of soil trace gas fluxes throughout the growing season toobtain high-temporal frequency data and to provide insights into magnitudesand temporal variability across rapidly changing conditions such as tidalcycles. We found that soil CO2 fluxes did not show a consistent dielpattern, CH4, N2O, and CS2 fluxes were highly variable withfrequent pulse emissions (> 2500 %, > 10 000 %,and > 4500 % change, respectively), and DMS fluxes onlyoccurred midday with changes > 185 000 %. When we comparedcontinuous measurements with discrete temporal measurements (during daytime,at low tide), discrete measurements of soil CO2 fluxes were comparablewith those from continuous measurements but misrepresent the temporalvariability and magnitudes of CH4, N2O, DMS, and CS2.Discrepancies between the continuous and discrete measurement data result indifferences for calculating the sustained global warming potential (SGWP),mainly by an overestimation of CH4 fluxes when using discretemeasurements. The high temporal variability of trace gas fluxes complicatesthe accurate calculation of budgets for use in blue carbon accounting andearth system models.
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The impacts of ocean acidification on marine trace gases and the implications for atmospheric chemistry and climate
Surface ocean biogeochemistry and photochemistry regulate ocean–atmosphere fluxes of trace gases critical for Earth's atmospheric chemistry and climate. The oceanic processes governing these fluxes are often sensitive to the changes in ocean pH (or p CO 2 ) accompanying ocean acidification (OA), with potential for future climate feedbacks. Here, we review current understanding (from observational, experimental and model studies) on the impact of OA on marine sources of key climate-active trace gases, including dimethyl sulfide (DMS), nitrous oxide (N 2 O), ammonia and halocarbons. We focus on DMS, for which available information is considerably greater than for other trace gases. We highlight OA-sensitive regions such as polar oceans and upwelling systems, and discuss the combined effect of multiple climate stressors (ocean warming and deoxygenation) on trace gas fluxes. To unravel the biological mechanisms responsible for trace gas production, and to detect adaptation, we propose combining process rate measurements of trace gases with longer term experiments using both model organisms in the laboratory and natural planktonic communities in the field. Future ocean observations of trace gases should be routinely accompanied by measurements of two components of the carbonate system to improve our understanding of how in situ carbonate chemistry influences trace gas production. Together, this will lead to improvements in current process model capabilities and more reliable predictions of future global marine trace gas fluxes.
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- Award ID(s):
- 1840868
- PAR ID:
- 10280244
- Author(s) / Creator(s):
- ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; ; more »
- Date Published:
- Journal Name:
- Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences
- Volume:
- 476
- Issue:
- 2237
- ISSN:
- 1364-5021
- Page Range / eLocation ID:
- 20190769
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1098/rspa.2019.0769
