Abstract. Most plot-scale methane emission models -of which many have been developed in the recent past -are validated using data collected with the closed-chamber technique. This method, however, suffers from a low spatial representativeness and a poor temporal resolution. Also, during a chamber-flux measurement the air within a chamber is separated from the ambient atmosphere, which negates the influence of wind on emissions.Additionally, some methane models are validated by upscaling fluxes based on the area-weighted averages of modelled fluxes, and by comparing those to the eddy covariance (EC) flux. This technique is rather inaccurate, as the area of upscaling might be different from the EC tower footprint, therefore introducing significant mismatch.In this study, we present an approach to validate plot-scale methane models with EC observations using the footprintweighted average method. Our results show that the fluxes obtained by the footprint-weighted average method are of the same magnitude as the EC flux. More importantly, the temporal dynamics of the EC flux on a daily timescale are also captured (r 2 = 0.7). In contrast, using the area-weighted average method yielded a low (r 2 = 0.14) correlation with the EC measurements. This shows that the footprint-weighted average method is preferable when validating methane emission models with EC fluxes for areas with a heterogeneous and irregular vegetation pattern.
The Arctic is rapidly transitioning toward a seasonal sea ice‐free state, perhaps one of the most apparent examples of climate change in the world. This dramatic change has numerous consequences, including a large increase in air temperatures, which in turn may affect terrestrial methane emissions. Nonetheless, terrestrial and marine environments are seldom jointly analyzed. By comparing satellite observations of Arctic sea ice concentrations to methane emissions simulated by three process‐based biogeochemical models, this study shows that rising wetland methane emissions are associated with sea ice retreat. Our analyses indicate that simulated high‐latitude emissions for 2005–2010 were, on average, 1.7 Tg CH 4 yr −1 higher compared to 1981–1990 due to a sea ice‐induced, autumn‐focused, warming. Since these results suggest a continued rise in methane emissions with future sea ice decline, observation programs need to include measurements during the autumn to further investigate the impact of this spatial connection on terrestrial methane emissions.
Abstract. In order to better address the feedbacks between climate and wetland methane (CH 4 ) emissions, we tested several mechanistic improvements to the wetland CH 4 emission model Peatland-VU with a longer Arctic data set than any other model: (1) inclusion of an improved hydrological module, (2) incorporation of a gross primary productivity (GPP) module, and (3) a more realistic soil-freezing scheme.A long time series of field measurements (2003-2010) from a tundra site in northeastern Siberia is used to validate the model, and the generalized likelihood uncertainty estimation (GLUE) methodology is used to test the sensitivity of model parameters.Peatland-VU is able to capture both the annual magnitude and seasonal variations of the CH 4 flux, water table position, and soil thermal properties. However, detailed daily variations are difficult to evaluate due to data limitation. Improvements due to the inclusion of a GPP module are less than anticipated, although this component is likely to become more important at larger spatial scales because the module can accommodate the variations in vegetation traits better than at plot scale.Sensitivity experiments suggest that the methane production rate factor, the methane plant oxidation parameter, the reference temperature for temperature-dependent decomposition, and the methane plant transport rate factor are the most important parameters affecting the data fit, regardless of vegetation type. Both wet and dry vegetation cover are sensitive to the minimum water table level; the former is also sensitive to the runoff threshold and open water correction factor, and the latter to the subsurface water evaporation and evapotranspiration correction factors.These results shed light on model parameterization and future improvement of CH 4 modelling. However, high spatial variability of CH 4 emissions within similar vegetation/soil units and data quality prove to impose severe limits on model testing and improvement.
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