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Inland waters play a major role in global greenhouse gas (GHG) budgets. The smallest of these systems (i.e., ponds) have a particularly large—but poorly constrained—emissions footprint at the global scale. Much of this uncertainty is due to a poor understanding of temporal variability in emissions. Here, we conducted high‐resolution temporal sampling to quantify GHG exchange between four temperate constructed ponds and the atmosphere on an annual basis. We show these ponds are a net source of GHGs to the atmosphere (564.4 g CO₂‐eq m⁻² yr⁻¹), driven by highly temporally variable diffusive methane (CH₄) emissions. Diffusive CH₄release to the atmosphere was twice as high during periods when the ponds had a stratified water column than when it was mixed. Ebullitive CH₄release was also higher during stratification. Building ponds to favor mixed conditions thus presents an opportunity to minimize the global GHG footprint of future pond construction.

 

Small waterbodies have potentially high greenhouse gas emissions relative to their small footprint on the landscape, although there is high uncertainty in model estimates. Scaling their carbon dioxide (CO₂) and methane (CH₄) exchange with the atmosphere remains challenging due to an incomplete understanding and characterization of spatial and temporal variability in CO₂and CH₄. Here, we measured partial pressures of CO₂(pCO₂) and CH₄(pCH₄) across 30 ponds and shallow lakes during summer in temperate regions of Europe and North America. We sampled each waterbody in three locations at three times during the growing season, and tested which physical, chemical, and biological characteristics related to the means and variability ofpCO₂andpCH₄in space and time. Summer means ofpCO₂andpCH₄were inversely related to waterbody size and positively related to floating vegetative cover;pCO₂was also positively related to dissolved phosphorus. Temporal variability in partial pressure in both gases weas greater than spatial variability. Although sampling on a single date was likely to misestimate mean seasonalpCO₂by up to 26%, mean seasonalpCH₄could be misestimated by up to 64.5%. Shallower systems displayed the most temporal variability inpCH₄and waterbodies with more vegetation cover had lower temporal variability. Inland waters remain one of the most uncertain components of the global carbon budget; understanding spatial and temporal variability will ultimately help us to constrain our estimates and inform research priorities.

 

Abstract. In the current era of rapid climate change, accuratecharacterization of climate-relevant gas dynamics – namely production,consumption, and net emissions – is required for all biomes, especially thoseecosystems most susceptible to the impact of change. Marine environmentsinclude regions that act as net sources or sinks for numerous climate-activetrace gases including methane (CH4) and nitrous oxide (N2O). Thetemporal and spatial distributions of CH4 and N2O are controlledby the interaction of complex biogeochemical and physical processes. Toevaluate and quantify how these mechanisms affect marine CH4 andN2O cycling requires a combination of traditional scientificdisciplines including oceanography, microbiology, and numerical modeling.Fundamental to these efforts is ensuring that the datasets produced byindependent scientists are comparable and interoperable. Equally critical istransparent communication within the research community about the technicalimprovements required to increase our collective understanding of marineCH4 and N2O. A workshop sponsored by Ocean Carbon and Biogeochemistry (OCB)was organized to enhance dialogue and collaborations pertaining tomarine CH4 and N2O. Here, we summarize the outcomes from theworkshop to describe the challenges and opportunities for near-futureCH4 and N2O research in the marine environment.