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Abstract Coastal salt marshes store large amounts of carbon but the magnitude and patterns of greenhouse gas (GHG; i.e., carbon dioxide (CO2) and methane (CH4)) fluxes are unclear. Information about GHG fluxes from these ecosystems comes from studies of sediments or at the ecosystem‐scale (eddy covariance) but fluxes from tidal creeks are unknown. We measured GHG concentrations in water, water quality, meteorological parameters, sediment CO2efflux, ecosystem‐scale GHG fluxes, and plant phenology; all at half‐hour intervals over 1 year. Manual creek GHG flux measurements were used to calculate gas transfer velocity (k) and parameterize a model of water‐to‐atmosphere GHG fluxes. The creek was a source of GHGs to the atmosphere where tidal patterns controlled diel variability. Dissolved oxygen and wind speed were negatively correlated with creek CH4efflux. Despite lacking a seasonal pattern, creek CO2efflux was correlated with drivers such as turbidity across phenological phases. Overall, nighttime creek CO2efflux (3.6 ± 0.63 μmol/m2/s) was at least 2 times higher than nighttime marsh sediment CO2efflux (1.5 ± 1.23 μmol/m2/s). Creek CH4efflux (17.5 ± 6.9 nmol/m2/s) was 4 times lower than ecosystem‐scale CH4fluxes (68.1 ± 52.3 nmol/m2/s) across the year. These results suggest that tidal creeks are potential hotspots for CO2emissions and could contribute to lateral transport of CH4to the coastal ocean due to supersaturation of CH4(>6,000 μmol/mol) in water. This study provides insights for modeling GHG efflux from tidal creeks and suggests that changes in tide stage overshadow water temperature in determining magnitudes of fluxes.
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High methane concentrations in tidal salt marsh soils: Where does the methane go?
Abstract Tidal salt marshes produce and emit CH4. Therefore, it is critical to understand the biogeochemical controls that regulate CH4spatial and temporal dynamics in wetlands. The prevailing paradigm assumes that acetoclastic methanogenesis is the dominant pathway for CH4production, and higher salinity concentrations inhibit CH4production in salt marshes. Recent evidence shows that CH4is produced within salt marshes via methylotrophic methanogenesis, a process not inhibited by sulfate reduction. To further explore this conundrum, we performed measurements of soil–atmosphere CH4and CO2fluxes coupled with depth profiles of soil CH4and CO2pore water gas concentrations, stable and radioisotopes, pore water chemistry, and microbial community composition to assess CH4production and fate within a temperate tidal salt marsh. We found unexpectedly high CH4concentrations up to 145,000 μmol mol−1positively correlated with S2−(salinity range: 6.6–14.5 ppt). Despite large CH4production within the soil, soil–atmosphere CH4fluxes were low but with higher emissions and extreme variability during plant senescence (84.3 ± 684.4 nmol m−2 s−1). CH4and CO2within the soil pore water were produced from young carbon, with most Δ14C‐CH4and Δ14C‐CO2values at or above modern. We found evidence that CH4within soils was produced by methylotrophic and hydrogenotrophic methanogenesis. Several pathways exist after CH4is produced, including diffusion into the atmosphere, CH4oxidation, and lateral export to adjacent tidal creeks; the latter being the most likely dominant flux. Our findings demonstrate that CH4production and fluxes are biogeochemically heterogeneous, with multiple processes and pathways that can co‐occur and vary in importance over the year. This study highlights the potential for high CH4production, the need to understand the underlying biogeochemical controls, and the challenges of evaluating CH4budgets and blue carbon in salt marshes.
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- Award ID(s):
- 1652594
- PAR ID:
- 10478187
- Publisher / Repository:
- Wiley-Blackwell
- Date Published:
- Journal Name:
- Global Change Biology
- Volume:
- 30
- Issue:
- 1
- ISSN:
- 1354-1013
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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