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Abstract Tropical wetlands and freshwaters are major contributors to the growing atmospheric methane (CH₄) burden. Extensive peatland drainage has lowered CH₄emissions from peat soils in Southeast Asia, but the canals draining these peatlands may be hotspots of CH₄emissions. Alternatively, CH₄oxidation (consumption) by methanotrophic microorganisms may attenuate emissions. Here, we used laboratory experiments and a synoptic survey of the isotopic composition of CH₄in 34 canals across West Kalimantan, Indonesia to quantify the proportion of CH₄that is consumed and therefore not emitted to the atmosphere. We find that CH₄oxidation mitigates 76.4 ± 12.0% of potential canal emissions, reducing emissions by ~70 mg CH₄m⁻²d⁻¹. Methane consumption also significantly impacts the stable isotopic fingerprint of canal CH₄emissions. As canals drain over 65% of peatlands in Southeast Asia, our results suggest that CH₄oxidation significantly influences landscape-scale CH₄emissions from these ecosystems. 

To understand patterns in CO2 partial pressure (PCO2) over time in wetlands’ surface water and porewater, we examined the relationship between PCO2 and land–atmosphere flux of CO2 at the ecosystem scale at 22 Northern Hemisphere wetland sites synthesized through an open call. Sites spanned 6 major wetland types (tidal, alpine, fen, bog, marsh, and prairie pothole/karst), 7 Köppen climates, and 16 different years. Ecosystem respiration (Reco) and gross primary production (GPP), components of vertical CO2 flux, were compared to PCO2, a component of lateral CO2 flux, to determine if photosynthetic rates and soil respiration consistently influence wetland surface and porewater CO2 concentrations across wetlands. Similar to drivers of primary productivity at the ecosystem scale, PCO2 was strongly positively correlated with air temperature (Tair) at most sites. Monthly average PCO2 tended to peak towards the middle of the year and was more strongly related to Reco than GPP. Our results suggest Reco may be related to biologically driven PCO2 in wetlands, but the relationship is site-specific and could be an artifact of differently timed seasonal cycles or other factors. Higher levels of discharge do not consistently alter the relationship between Reco and temperature normalized PCO2. This work synthesizes relevant data and identifies key knowledge gaps in drivers of wetland respiration. 

Abstract Methane (CH₄) is a potent greenhouse gas (GHG) with atmospheric concentrations that have nearly tripled since pre‐industrial times. Wetlands account for a large share of global CH₄emissions, yet the magnitude and factors controlling CH₄fluxes in tidal wetlands remain uncertain. We synthesized CH₄flux data from 100 chamber and 9 eddy covariance (EC) sites across tidal marshes in the conterminous United States to assess controlling factors and improve predictions of CH₄emissions. This effort included creating an open‐source database of chamber‐based GHG fluxes (https://doi.org/10.25573/serc.14227085). Annual fluxes across chamber and EC sites averaged 26 ± 53 g CH₄m⁻² year⁻¹, with a median of 3.9 g CH₄m⁻² year⁻¹, and only 25% of sites exceeding 18 g CH₄m⁻² year⁻¹. The highest fluxes were observed at fresh‐oligohaline sites with daily maximum temperature normals (MATmax) above 25.6°C. These were followed by frequently inundated low and mid‐fresh‐oligohaline marshes with MATmax ≤25.6°C, and mesohaline sites with MATmax >19°C. Quantile regressions of paired chamber CH₄flux and porewater biogeochemistry revealed that the 90th percentile of fluxes fell below 5 ± 3 nmol m⁻² s⁻¹at sulfate concentrations >4.7 ± 0.6 mM, porewater salinity >21 ± 2 psu, or surface water salinity >15 ± 3 psu. Across sites, salinity was the dominant predictor of annual CH₄fluxes, while within sites, temperature, gross primary productivity (GPP), and tidal height controlled variability at diel and seasonal scales. At the diel scale, GPP preceded temperature in importance for predicting CH₄flux changes, while the opposite was observed at the seasonal scale. Water levels influenced the timing and pathway of diel CH₄fluxes, with pulsed releases of stored CH₄at low to rising tide. This study provides data and methods to improve tidal marsh CH₄emission estimates, support blue carbon assessments, and refine national and global GHG inventories.