Practical Guide to Measuring Wetland Carbon Pools and Fluxes.

Wetlands cover a small portion of the world, but have disproportionate influence on global carbon (C) sequestration, carbon dioxide and methane emissions, and aquatic C fluxes. However, the underlying biogeochemical processes that affect wetland C pools and fluxes are complex and dynamic, making measurements of wetland C challenging. Over decades of research, many observational, experimental, and analytical approaches have been developed to understand and quantify pools and fluxes of wetland C. Sampling approaches range in their representation of wetland C from short to long timeframes and local to landscape spatial scales. This review summarizes common and cutting-edge methodological approaches for quantifying wetland C pools and fluxes. We first define each of the major C pools and fluxes and provide rationale for their importance to wetland C dynamics. For each approach, we clarify what component of wetland C is measured and its spatial and temporal representativeness and constraints. We describe practical considerations for each approach, such as where and when an approach is typically used, who can conduct the measurements (expertise, training requirements), and how approaches are conducted, including considerations on equipment complexity and costs. Finally, we review key covariates and ancillary measurements that enhance the interpretation of findings and facilitate model development. The protocols that we describe to measure soil, water, vegetation, and gases are also relevant for related disciplines such as ecology. Improved quality and consistency of data collection and reporting across studies will help reduce global uncertainties and develop management strategies to use wetlands as nature-based climate solutions. Supplementary Information: The online version contains supplementary material available at 10.1007/s13157-023-01722-2.

Evaluation of the methane paradox in four adjacent pre-alpine lakes across a trophic gradient.

Contrasting the paradigm that methane is only produced in anoxic conditions, recent discoveries show that oxic methane production (OMP, aka the methane paradox) occurs in oxygenated surface waters worldwide. OMP drivers and their contribution to global methane emissions, however, are not well constrained. In four adjacent pre-alpine lakes, we determine the net methane production rates in oxic surface waters using two mass balance approaches, accounting for methane sources and sinks. We find that OMP occurs in three out of four studied lakes, often as the dominant source of diffusive methane emissions. Correlations of net methane production versus chlorophyll-a, Secchi and surface mixed layer depths suggest a link with photosynthesis and provides an empirical upscaling approach. As OMP is a methane source in direct contact with the atmosphere, a better understanding of its extent and drivers is necessary to constrain the atmospheric methane contribution by inland waters.

Interannual, summer, and diel variability of CH4 and CO2 effluxes from Toolik Lake, Alaska, during the ice-free periods 2010-2015.

Accelerated warming in the Arctic has led to concern regarding the amount of carbon emission potential from Arctic water bodies. Yet, aquatic carbon dioxide (CO2) and methane (CH4) flux measurements remain scarce, particularly at high resolution and over long periods of time. Effluxes of methane (CH4) and carbon dioxide (CO2) from Toolik Lake, a deep glacial lake in northern Alaska, were measured for the first time with the direct eddy covariance (EC) flux technique during six ice-free lake periods (2010-2015). CO2 flux estimates from the lake (daily average efflux of 16.7 ± 5.3 mmol m-2 d-1) were in good agreement with earlier estimates from 1975-1989 using different methods. CH4 effluxes in 2010-2015 (averaging 0.13 ± 0.06 mmol m-2 d-1) showed an interannual variation that was 4.1 times greater than median diel variations, but mean fluxes were almost one order of magnitude lower than earlier estimates obtained from single water samples in 1990 and 2011-2012. The overall global warming potential (GWP) of Toolik Lake is thus governed mostly by CO2 effluxes, contributing 86-93% of the ice-free period GWP of 26-90 g CO2,eq m-2. Diel variation in fluxes was also important, with up to a 2-fold (CH4) to 4-fold (CO2) difference between the highest nighttime and lowest daytime effluxes. Within the summer ice-free period, on average, CH4 fluxes increased 2-fold during the first half of the summer, then remained almost constant, whereas CO2 effluxes remained almost constant over the entire summer, ending with a linear increase during the last 1-2 weeks of measurements. Due to the cold bottom temperatures of this 26 m deep lake, and the absence of ebullition and episodic flux events, Toolik Lake and other deep glacial lakes are likely not hot spots for greenhouse gas emissions, but they still contribute to the overall GWP of the Arctic.

Eutrophication will increase methane emissions from lakes and impoundments during the 21st century.

Lakes and impoundments are an important source of methane (CH4), a potent greenhouse gas, to the atmosphere. A recent analysis shows aquatic productivity (i.e., eutrophication) is an important driver of CH4 emissions from lentic waters. Considering that aquatic productivity will increase over the next century due to climate change and a growing human population, a concomitant increase in aquatic CH4 emissions may occur. We simulate the eutrophication of lentic waters under scenarios of future nutrient loading to inland waters and show that enhanced eutrophication of lakes and impoundments will substantially increase CH4 emissions from these systems (+30-90%) over the next century. This increased CH4 emission has an atmospheric impact of 1.7-2.6 Pg C-CO2-eq y-1, which is equivalent to 18-33% of annual CO2 emissions from burning fossil fuels. Thus, it is not only important to limit eutrophication to preserve fragile water supplies, but also to avoid acceleration of climate change.

Greenhouse gas emissions from lakes and impoundments: upscaling in the face of global change.

Lakes and impoundments are important sources of greenhouse gases (GHG: i.e., CO2, CH4, N2O), yet global emission estimates are based on regionally-biased averages and elementary upscaling. We assembled the largest global dataset to date on emission rates of all three GHGs and found they covary with lake size and trophic state. Fitted models were upscaled to estimate global emission using global lake size inventories and a remotely-sensed global lake productivity distribution. Traditional upscaling approaches overestimated CO2 and N2O emission but underestimated CH4 by half. Our upscaled size-productivity weighted estimates (1.25-2.30 Pg of CO2-equivalents annually) are nearly 20% of global CO2 fossil fuel emission with ~75% of the climate impact due to CH4. Moderate global increases in eutrophication could translate to 5-40% increases in the GHG effects in the atmosphere, adding the equivalent effect of another 13% of fossil fuel combustion or an effect equal to GHG emissions from current land use change.

Greenhouse Gas Emissions from Freshwater Reservoirs: What Does the Atmosphere See?

Freshwater reservoirs are a known source of greenhouse gas (GHG) to the atmosphere, but their quantitative significance is still only loosely con- strained. Although part of this uncertainty can be attributed to the difficulties in measuring highly variable fluxes, it is also the result of a lack of a clear accounting methodology, particularly about what constitutes new emissions and potential new sinks. In this paper, we review the main processes involved in the generation of GHG in reservoir systems and propose a simple approach to quantify the reservoir GHG footprint in terms of the net changes in GHG fluxes to the atmosphere induced by damming, that is, 'what the atmosphere sees.' The approach takes into account the pre-impoundment GHG balance of the landscape, the temporal evolution of reservoir GHG emission profile as well as the natural emissions that are displaced to or away from the reservoir site resulting from hydrological and other changes. It also clarifies the portion of the reservoir carbon burial that can potentially be considered an offset to GHG emissions.

Cross continental increase in methane ebullition under climate change.

Methane (CH4) strongly contributes to observed global warming. As natural CH4 emissions mainly originate from wet ecosystems, it is important to unravel how climate change may affect these emissions. This is especially true for ebullition (bubble flux from sediments), a pathway that has long been underestimated but generally dominates emissions. Here we show a remarkably strong relationship between CH4 ebullition and temperature across a wide range of freshwater ecosystems on different continents using multi-seasonal CH4 ebullition data from the literature. As these temperature-ebullition relationships may have been affected by seasonal variation in organic matter availability, we also conducted a controlled year-round mesocosm experiment. Here 4 °C warming led to 51% higher total annual CH4 ebullition, while diffusion was not affected. Our combined findings suggest that global warming will strongly enhance freshwater CH4 emissions through a disproportional increase in ebullition (6-20% per 1 °C increase), contributing to global warming.

Minor methane emissions from an Alpine hydropower reservoir based on monitoring of diel and seasonal variability.

We monitored CH4 emissions during the ice-free period of an Alpine hydropower reservoir in the Swiss Alps, Lake Klöntal, to investigate mechanisms responsible for CH4 variability and to estimate overall emissions to the atmosphere. A floating eddy-covariance platform yielded total CH4 and CO2 emission rates at high temporal resolution, while hydroacoustic surveys provided no indication of CH4 ebullition. Higher CH4 fluxes (2.9 ± 0.1 mg CH4 per m2 per day) occurred during the day when surface water temperatures were warmer and wind speeds higher than at night. Piston velocity estimates (k600) showed an upper limit at high wind speeds that may be more generally valid also for other lakes and reservoirs with limited CH4 dissolved in the water body: above 2.0 m s-1 a further increase in wind speed did not lead to higher CH4 fluxes, because under such conditions it is not the turbulent mixing and transport that limits effluxes, but the resupply of CH4 to the lake surface. Increasing CH4 fluxes during the warm season showed a clear spatial gradient once the reservoir started to fill up and flood additional surface area. The warm period contributed 27% of the total CH4 emissions (2.6 t CH4 per year) estimated for the full year and CH4 accounted for 63% of carbonic greenhouse gas emissions. Overall, the average CH4 emissions (1.7 to 2.2 mg CH4 per m2 per day determined independently from surface water samplings and eddy covariance, respectively) were small compared to most tropical and some temperate reservoirs. The resulting greenhouse gas (GHG) emissions in CO2-equivalents revealed that electricity produced in the Lake Klöntal power plant was relatively climate-friendly with a low GHG-to-power output ratio of 1.24 kg CO2,eq per MW h compared to 6.5 and 8.1 kg CO2,eq per MW h associated with the operation of solar photovoltaics and wind energy, respectively, or about 980 kg CO2,eq per MW h for coal-fired power plants.

Greenhouse Gas Emissions from Reservoir Water Surfaces: A New Global Synthesis.

Collectively, reservoirs created by dams are thought to be an important source of greenhouse gases (GHGs) to the atmosphere. So far, efforts to quantify, model, and manage these emissions have been limited by data availability and inconsistencies in methodological approach. Here, we synthesize reservoir CH4, CO2, and N2O emission data with three main objectives: (1) to generate a global estimate of GHG emissions from reservoirs, (2) to identify the best predictors of these emissions, and (3) to consider the effect of methodology on emission estimates. We estimate that GHG emissions from reservoir water surfaces account for 0.8 (0.5-1.2) Pg CO2 equivalents per year, with the majority of this forcing due to CH4. We then discuss the potential for several alternative pathways such as dam degassing and downstream emissions to contribute significantly to overall emissions. Although prior studies have linked reservoir GHG emissions to reservoir age and latitude, we find that factors related to reservoir productivity are better predictors of emission.

Sediment trapping by dams creates methane emission hot spots.

Inland waters transport and transform substantial amounts of carbon and account for ∼18% of global methane emissions. Large reservoirs with higher areal methane release rates than natural waters contribute significantly to freshwater emissions. However, there are millions of small dams worldwide that receive and trap high loads of organic carbon and can therefore potentially emit significant amounts of methane to the atmosphere. We evaluated the effect of damming on methane emissions in a central European impounded river. Direct comparison of riverine and reservoir reaches, where sedimentation in the latter is increased due to trapping by dams, revealed that the reservoir reaches are the major source of methane emissions (∼0.23 mmol CH4 m(-2) d(-1) vs ∼19.7 mmol CH4 m(-2) d(-1), respectively) and that areal emission rates far exceed previous estimates for temperate reservoirs or rivers. We show that sediment accumulation correlates with methane production and subsequent ebullitive release rates and may therefore be an excellent proxy for estimating methane emissions from small reservoirs. Our results suggest that sedimentation-driven methane emissions from dammed river hot spot sites can potentially increase global freshwater emissions by up to 7%.

Spatial heterogeneity of methane ebullition in a large tropical reservoir.

Tropical reservoirs have been identified as important methane (CH(4)) sources to the atmosphere, primarily through turbine and downstream degassing. However, the importance of ebullition (gas bubbling) remains unclear. We hypothesized that ebullition is a disproportionately large CH(4) source from reservoirs with dendritic littoral zones because of ebullition hot spots occurring where rivers supply allochthonous organic material. We explored this hypothesis in Lake Kariba (Zambia/Zimbabwe; surface area >5000 km(2)) by surveying ebullition in bays with and without river inputs using an echosounder and traditional surface chambers. The two techniques yielded similar results, and revealed substantially higher fluxes in river deltas (∼10(3) mg CH(4) m(-2) d(-1)) compared to nonriver bays (<100 mg CH(4) m(-2) d(-1)). Hydroacoustic measurements resolved at 5 m intervals showed that flux events varied over several orders of magnitude (up to 10(5) mg CH(4) m(-2) d(-1)), and also identified strong differences in ebullition frequency. Both factors contributed to emission differences between all sites. A CH(4) mass balance for the deepest basin of Lake Kariba indicated that hot spot ebullition was the largest atmospheric emission pathway, suggesting that future greenhouse gas budgets for tropical reservoirs should include a spatially well-resolved analysis of ebullition hot spots.

Extreme methane emissions from a Swiss hydropower reservoir: contribution from bubbling sediments.

Methane emission pathways and their importance were quantified during a yearlong survey of a temperate hydropower reservoir. Measurements using gas traps indicated very high ebullition rates, but due to the stochastic nature of ebullition a mass balance approach was crucial to deduce system-wide methane sources and losses. Methane diffusion from the sediment was generally low and seasonally stable and did not account for the high concentration of dissolved methane measured in the reservoir discharge. A strong positive correlation between water temperature and the observed dissolved methane concentration enabled us to quantify the dissolved methane addition from bubble dissolution using a system-wide mass balance. Finally, knowing the contribution due to bubble dissolution, we used a bubble model to estimate bubble emission directly to the atmosphere. Our results indicated that the total methane emission from Lake Wohlen was on average >150 mg CH(4) m(-2) d(-1), which is the highest ever documented for a midlatitude reservoir. The substantial temperature-dependent methane emissions discovered in this 90-year-old reservoir indicate that temperate water bodies can be an important but overlooked methane source.