Abstract. Natural wetlands constitute the largest and most uncertain source of methane (CH4) to the atmosphere and a large fraction of them are found in the northern latitudes. These emissions are typically estimated using process (“bottom-up”) or inversion (“top-down”) models. However, estimates from these two types of models are not independent of each other since the top-down estimates usually rely on the a priori estimation of these emissions obtained with process models. Hence, independent spatially explicit validation data are needed. Here we utilize a random forest (RF) machine-learning technique to upscale CH4 eddy covariance flux measurements from 25 sites to estimate CH4 wetland emissions from the northern latitudes (north of 45∘ N). Eddy covariance data from 2005 to 2016 are used for model development. The model is then used to predict emissions during 2013 and 2014. The predictive performance of the RF model is evaluated using a leave-one-site-out cross-validation scheme. The performance (Nash–Sutcliffe model efficiency =0.47) is comparable to previous studies upscaling net ecosystem exchange of carbon dioxide and studies comparing process model output against site-level CH4 emission data. The global distribution of wetlands is one major source of uncertainty for upscaling CH4. Thus, three wetland distribution maps are utilized in the upscaling. Depending on the wetland distribution map, the annual emissions for the northern wetlands yield 32 (22.3–41.2, 95 % confidence interval calculated from a RF model ensemble), 31 (21.4–39.9) or 38 (25.9–49.5) Tg(CH4) yr−1. To further evaluate the uncertainties of the upscaled CH4 flux data products we also compared them against output from two process models (LPX-Bern and WetCHARTs), and methodological issues related to CH4 flux upscaling are discussed. The monthly upscaled CH4 flux data products are available at https://doi.org/10.5281/zenodo.2560163 (Peltola et al., 2019).
Abstract. Natural wetlands constitute the largest and most uncertain source of methane (CH4) to the atmosphere and a large fraction of them are in the northern latitudes. These emissions are typically estimated using process (bottom-up) or inversion (top-down) models, yet the two are not independent of each other since the top-down estimates rely on the a priori estimation of these emissions coming from the process models. Hence, independent validation data of the large-scale emissions would be needed. Here we utilize random forest (RF) machine learning technique to upscale CH4 eddy covariance flux measurements from 25 sites to estimate CH4 wetland emissions from the northern latitudes (north of 45 °N) during years 2013 and 2014. The predictive performance of the RF model is evaluated using the leave-one-site-out cross-validation scheme and the performance (Nash-Sutcliffe model efficiency = 0.47) is comparable to previous studies upscaling net ecosystem exchange of carbon dioxide or studies where process models are compared against site-level CH4 emission data. Three wetland maps are utilized in the upscaling and the annual emissions for the northern wetlands yield 31.7 (22.3–41.2, 95 % confidence interval), 30.6 (21.4–39.9) or 37.6 (25.9–49.5) Tg(CH4) yr−1, depending on the map used. To evaluate the uncertainties of the upscaled product it is also compared against two process models (LPX-Bern and WetCHARTs) and methodological issues related to CH4 flux upscaling are discussed. The monthly upscaled CH4 flux data product is available for further usage at: https://doi.org/10.5281/zenodo.2560164.
During August 2016, a quasi-stationary high-pressure system spreading over Central and NorthEastern Europe, caused weather conditions that allowed for 24/7 observations of aerosol optical properties by using a complex multi-wavelength PollyXT lidar system with Raman, polarization and water vapour capabilities, based at the European Aerosol Research Lidar Network (EARLINET network) urban site in Warsaw, Poland. During 24-30 August 2016, the lidar-derived products (boundary layer height, aerosol optical depth, Ångström exponent, lidar ratio, depolarization ratio) were analysed in terms of air mass transport (HYSPLIT model), aerosol load (CAMS data) and type (NAAPS model) and confronted with active and passive remote sensing at the ground level (PolandAOD, AERONET, WIOS-AQ networks) and aboard satellites (SEVIRI, MODIS, CATS sensors). Optical properties for less than a day-old fresh biomass burning aerosol, advected into Warsaw's boundary layer from over Ukraine, were compared with the properties of long-range transported 3-5 day-old aged biomass burning aerosol detected in the free troposphere over Warsaw. Analyses of temporal changes of aerosol properties within the
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