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  • 1
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 23, No. 17 ( 2023-09-08), p. 10035-10056
    Abstract: Abstract. Carbonyl sulfide (OCS) has emerged as a valuable proxy for photosynthetic uptake of carbon dioxide (CO2) and is known to be important in the formation of aerosols in the stratosphere. However, uncertainties in the global OCS budget remain large. This is mainly due to the following three flux terms: vegetation uptake, soil uptake and oceanic emissions. Bottom-up estimates do not yield a closed budget, which is thought to be due to tropical emissions of OCS that are not accounted for. Here we present a simulation of atmospheric OCS over the period 2004–2018 using the TOMCAT 3-D chemical transport model that is aimed at better constraining some terms in the OCS budget. Vegetative uptake of OCS is estimated by scaling gross primary productivity (GPP) output from the Joint UK Land Environment Simulator (JULES) using the leaf relative uptake (LRU) approach. The remaining surface budget terms are taken from available literature flux inventories and adequately scaled to bring the budget into balance. The model is compared with limb-sounding satellite observations made by the Atmospheric Chemistry Experiment – Fourier Transform Spectrometer (ACE-FTS) and surface flask measurements from 14 National Oceanic and Atmospheric Administration – Earth System Research Laboratory (NOAA-ESRL) sites worldwide. We find that calculating vegetative uptake using the LRU underestimates the surface seasonal cycle amplitude (SCA) in the Northern Hemisphere (NH) mid-latitudes and high latitudes by approximately 37 ppt (35 %). The inclusion of a large tropical source is able to balance the global budget, but further improvement to the SCA and phasing would likely require a flux inversion scheme. Compared to co-located ACE-FTS OCS profiles between 5 and 30 km, TOMCAT remains within 25 ppt (approximately 5 % of mean tropospheric concentration) of the measurements throughout the majority of this region and lies within the standard deviation of these measurements. This provides confidence in the representation of atmospheric loss and surface fluxes of OCS in the model. Atmospheric sinks account for 154 Gg S of the annual budget, which is 10 %–50 % larger than previous studies. Comparing the surface monthly anomalies from the NOAA-ESRL flask data to the model simulations shows a root-mean-square error range of 3.3–25.8 ppt. We estimate the total biosphere uptake to be 951 Gg S, which is in the range of recent inversion studies (893–1053 Gg S), but our terrestrial vegetation flux accounts for 629 Gg S of the annual budget, which is lower than other recent studies (657–756 Gg S). However, to close the budget, we compensate for this with a large annual oceanic emission term of 689 Gg S focused over the tropics, which is much larger than bottom-up estimates (285 Gg S). Hence, we agree with recent findings that missing OCS sources likely originate from the tropical region. This work shows that satellite OCS profiles offer a good constraint on atmospheric sinks of OCS through the troposphere and stratosphere and are therefore useful for helping to improve surface budget terms. This work also shows that the LRU approach is an adequate representation of the OCS vegetative uptake, but this method could be improved by various means, such as using a higher-resolution GPP product or plant-functional-type-dependent LRU. Future work will utilise TOMCAT in a formal inversion scheme to better quantify the OCS budget.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2023
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  • 2
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 23, No. 17 ( 2023-09-01), p. 9685-9723
    Abstract: Abstract. Tropical forests such as the Amazonian rainforests play an important role for climate, are large carbon stores and are a treasure of biodiversity. Amazonian forests have been exposed to large-scale deforestation and degradation for many decades. Deforestation declined between 2005 and 2012 but more recently has again increased with similar rates as in 2007–2008. The resulting forest fragments are exposed to substantially elevated temperatures in an already warming world. These temperature and land cover changes are expected to affect the forests, and an important diagnostic of their health and sensitivity to climate variation is their carbon balance. In a recent study based on CO2 atmospheric vertical profile observations between 2010 and 2018, and an air column budgeting technique used to estimate fluxes, we reported the Amazon region as a carbon source to the atmosphere, mainly due to fire emissions. Instead of an air column budgeting technique, we use an inverse of the global atmospheric transport model, TOMCAT, to assimilate CO2 observations from Amazon vertical profiles and global flask measurements. We thus estimate inter- and intra-annual variability in the carbon fluxes, trends over time and controls for the period of 2010–2018. This is the longest period covered by a Bayesian inversion of these atmospheric CO2 profile observations to date. Our analyses indicate that the Amazon is a small net source of carbon to the atmosphere (mean 2010–2018 = 0.13 ± 0.17 Pg C yr−1, where 0.17 is the 1σ uncertainty), with the majority of the emissions coming from the eastern region (77 % of total Amazon emissions). Fire is the primary driver of the Amazonian source (0.26 ± 0.13 Pg C yr−1), while forest carbon uptake removes around half of the fire emissions to the atmosphere (−0.13 ± 0.20 Pg C yr−1). The largest net carbon sink was observed in the western-central Amazon region (72 % of the fire emissions). We find larger carbon emissions during the extreme drought years (such as 2010, 2015 and 2016), correlated with increases in temperature, cumulative water deficit and burned area. Despite the increase in total carbon emissions during drought years, we do not observe a significant trend over time in our carbon total, fire and net biome exchange estimates between 2010 and 2018. Our analysis thus cannot provide clear evidence for a weakening of the carbon uptake by Amazonian tropical forests.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2023
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  • 3
    In: Earth System Science Data, Copernicus GmbH, Vol. 13, No. 5 ( 2021-05-28), p. 2307-2362
    Abstract: Abstract. Reliable quantification of the sources and sinks of greenhouse gases, together with trends and uncertainties, is essential to monitoring the progress in mitigating anthropogenic emissions under the Paris Agreement. This study provides a consolidated synthesis of CH4 and N2O emissions with consistently derived state-of-the-art bottom-up (BU) and top-down (TD) data sources for the European Union and UK (EU27 + UK). We integrate recent emission inventory data, ecosystem process-based model results and inverse modeling estimates over the period 1990–2017. BU and TD products are compared with European national greenhouse gas inventories (NGHGIs) reported to the UN climate convention UNFCCC secretariat in 2019. For uncertainties, we used for NGHGIs the standard deviation obtained by varying parameters of inventory calculations, reported by the member states (MSs) following the recommendations of the IPCC Guidelines. For atmospheric inversion models (TD) or other inventory datasets (BU), we defined uncertainties from the spread between different model estimates or model-specific uncertainties when reported. In comparing NGHGIs with other approaches, a key source of bias is the activities included, e.g., anthropogenic versus anthropogenic plus natural fluxes. In inversions, the separation between anthropogenic and natural emissions is sensitive to the geospatial prior distribution of emissions. Over the 2011–2015 period, which is the common denominator of data availability between all sources, the anthropogenic BU approaches are directly comparable, reporting mean emissions of 20.8 Tg CH4 yr−1 (EDGAR v5.0) and 19.0 Tg CH4 yr−1 (GAINS), consistent with the NGHGI estimates of 18.9 ± 1.7 Tg CH4 yr−1. The estimates of TD total inversions give higher emission estimates, as they also include natural emissions. Over the same period regional TD inversions with higher-resolution atmospheric transport models give a mean emission of 28.8 Tg CH4 yr−1. Coarser-resolution global TD inversions are consistent with regional TD inversions, for global inversions with GOSAT satellite data (23.3 Tg CH4 yr−1) and surface network (24.4 Tg CH4 yr−1). The magnitude of natural peatland emissions from the JSBACH–HIMMELI model, natural rivers and lakes emissions, and geological sources together account for the gap between NGHGIs and inversions and account for 5.2 Tg CH4 yr−1. For N2O emissions, over the 2011–2015 period, both BU approaches (EDGAR v5.0 and GAINS) give a mean value of anthropogenic emissions of 0.8 and 0.9 Tg N2O yr−1, respectively, agreeing with the NGHGI data (0.9 ± 0.6 Tg N2O yr−1). Over the same period, the average of the three total TD global and regional inversions was 1.3 ± 0.4 and 1.3 ± 0.1 Tg N2O yr−1, respectively. The TD and BU comparison method defined in this study can be operationalized for future yearly updates for the calculation of CH4 and N2O budgets both at the EU+UK scale and at the national scale. The referenced datasets related to figures are visualized at https://doi.org/10.5281/zenodo.4590875 (Petrescu et al., 2020b).
    Type of Medium: Online Resource
    ISSN: 1866-3516
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
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  • 4
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 16, No. 12 ( 2016-06-30), p. 7943-7956
    Abstract: Abstract. The growth in atmospheric methane (CH4) concentrations over the past 2 decades has shown large variability on a timescale of several years. Prior to 1999 the globally averaged CH4 concentration was increasing at a rate of 6.0 ppb yr−1, but during a stagnation period from 1999 to 2006 this growth rate slowed to 0.6 ppb yr−1. From 2007 to 2009 the growth rate again increased to 4.9 ppb yr−1. These changes in growth rate are usually ascribed to variations in CH4 emissions. We have used a 3-D global chemical transport model, driven by meteorological reanalyses and variations in global mean hydroxyl (OH) concentrations derived from CH3CCl3 observations from two independent networks, to investigate these CH4 growth variations. The model shows that between 1999 and 2006 changes in the CH4 atmospheric loss contributed significantly to the suppression in global CH4 concentrations relative to the pre-1999 trend. The largest factor in this is relatively small variations in global mean OH on a timescale of a few years, with minor contributions of atmospheric transport of CH4 to its sink region and of atmospheric temperature. Although changes in emissions may be important during the stagnation period, these results imply a smaller variation is required to explain the observed CH4 trends. The contribution of OH variations to the renewed CH4 growth after 2007 cannot be determined with data currently available.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2016
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  • 5
    In: Biogeosciences, Copernicus GmbH, Vol. 19, No. 24 ( 2022-12-16), p. 5779-5805
    Abstract: Abstract. Wetlands are the largest natural source of methane. The ability to model the emissions of methane from natural wetlands accurately is critical to our understanding of the global methane budget and how it may change under future climate scenarios. The simulation of wetland methane emissions involves a complicated system of meteorological drivers coupled to hydrological and biogeochemical processes. The Joint UK Land Environment Simulator (JULES) is a process-based land surface model that underpins the UK Earth System Model (UKESM) and is capable of generating estimates of wetland methane emissions. In this study, we use GOSAT satellite observations of atmospheric methane along with the TOMCAT global 3-D chemistry transport model to evaluate the performance of JULES in reproducing the seasonal cycle of methane over a wide range of tropical wetlands. By using an ensemble of JULES simulations with differing input data and process configurations, we investigate the relative importance of the meteorological driving data, the vegetation, the temperature dependency of wetland methane production and the wetland extent. We find that JULES typically performs well in replicating the observed methane seasonal cycle. We calculate correlation coefficients to the observed seasonal cycle of between 0.58 and 0.88 for most regions; however, the seasonal cycle amplitude is typically underestimated (by between 1.8 and 19.5 ppb). This level of performance is comparable to that typically provided by state-of-the-art data-driven wetland CH4 emission inventories. The meteorological driving data are found to be the most significant factor in determining the ensemble performance, with temperature dependency and vegetation having moderate effects. We find that neither wetland extent configuration outperforms the other, but this does lead to poor performance in some regions. We focus in detail on three African wetland regions (Sudd, Southern Africa and Congo) where we find the performance of JULES to be poor and explore the reasons for this in detail. We find that neither wetland extent configuration used is sufficient in representing the wetland distribution in these regions (underestimating the wetland seasonal cycle amplitude by 11.1, 19.5 and 10.1 ppb respectively, with correlation coefficients of 0.23, 0.01 and 0.31). We employ the Catchment-based Macro-scale Floodplain (CaMa-Flood) model to explicitly represent river and floodplain water dynamics and find that these JULES-CaMa-Flood simulations are capable of providing a wetland extent that is more consistent with observations in this regions, highlighting this as an important area for future model development.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2022
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  • 6
    In: Earth System Science Data, Copernicus GmbH, Vol. 15, No. 3 ( 2023-03-21), p. 1197-1268
    Abstract: Abstract. Knowledge of the spatial distribution of the fluxes of greenhouse gases (GHGs) and their temporal variability as well as flux attribution to natural and anthropogenic processes is essential to monitoring the progress in mitigating anthropogenic emissions under the Paris Agreement and to inform its global stocktake. This study provides a consolidated synthesis of CH4 and N2O emissions using bottom-up (BU) and top-down (TD) approaches for the European Union and UK (EU27 + UK) and updates earlier syntheses (Petrescu et al., 2020, 2021). The work integrates updated emission inventory data, process-based model results, data-driven sector model results and inverse modeling estimates, and it extends the previous period of 1990–2017 to 2019. BU and TD products are compared with European national greenhouse gas inventories (NGHGIs) reported by parties under the United Nations Framework Convention on Climate Change (UNFCCC) in 2021. Uncertainties in NGHGIs, as reported to the UNFCCC by the EU and its member states, are also included in the synthesis. Variations in estimates produced with other methods, such as atmospheric inversion models (TD) or spatially disaggregated inventory datasets (BU), arise from diverse sources including within-model uncertainty related to parameterization as well as structural differences between models. By comparing NGHGIs with other approaches, the activities included are a key source of bias between estimates, e.g., anthropogenic and natural fluxes, which in atmospheric inversions are sensitive to the prior geospatial distribution of emissions. For CH4 emissions, over the updated 2015–2019 period, which covers a sufficiently robust number of overlapping estimates, and most importantly the NGHGIs, the anthropogenic BU approaches are directly comparable, accounting for mean emissions of 20.5 Tg CH4 yr−1 (EDGARv6.0, last year 2018) and 18.4 Tg CH4 yr−1 (GAINS, last year 2015), close to the NGHGI estimates of 17.5±2.1 Tg CH4 yr−1. TD inversion estimates give higher emission estimates, as they also detect natural emissions. Over the same period, high-resolution regional TD inversions report a mean emission of 34 Tg CH4 yr−1. Coarser-resolution global-scale TD inversions result in emission estimates of 23 and 24 Tg CH4 yr−1 inferred from GOSAT and surface (SURF) network atmospheric measurements, respectively. The magnitude of natural peatland and mineral soil emissions from the JSBACH–HIMMELI model, natural rivers, lake and reservoir emissions, geological sources, and biomass burning together could account for the gap between NGHGI and inversions and account for 8 Tg CH4 yr−1. For N2O emissions, over the 2015–2019 period, both BU products (EDGARv6.0 and GAINS) report a mean value of anthropogenic emissions of 0.9 Tg N2O yr−1, close to the NGHGI data (0.8±55 % Tg N2O yr−1). Over the same period, the mean of TD global and regional inversions was 1.4 Tg N2O yr−1 (excluding TOMCAT, which reported no data). The TD and BU comparison method defined in this study can be operationalized for future annual updates for the calculation of CH4 and N2O budgets at the national and EU27 + UK scales. Future comparability will be enhanced with further steps involving analysis at finer temporal resolutions and estimation of emissions over intra-annual timescales, which is of great importance for CH4 and N2O, and may help identify sector contributions to divergence between prior and posterior estimates at the annual and/or inter-annual scale. Even if currently comparison between CH4 and N2O inversion estimates and NGHGIs is highly uncertain because of the large spread in the inversion results, TD inversions inferred from atmospheric observations represent the most independent data against which inventory totals can be compared. With anticipated improvements in atmospheric modeling and observations, as well as modeling of natural fluxes, TD inversions may arguably emerge as the most powerful tool for verifying emission inventories for CH4, N2O and other GHGs. The referenced datasets related to figures are visualized at https://doi.org/10.5281/zenodo.7553800 (Petrescu et al., 2023).
    Type of Medium: Online Resource
    ISSN: 1866-3516
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2023
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  • 7
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 23, No. 13 ( 2023-07-05), p. 7363-7382
    Abstract: Abstract. Atmospheric methane (CH4) concentrations are rising, which are expected to lead to a corresponding increase in the global seasonal cycle amplitude (SCA) – the difference between its seasonal maximum and minimum values. The reaction between CH4 and its main sink, OH, is dependent on the amount of CH4 and OH in the atmosphere. The concentration of OH varies seasonally, and due to the increasing burden of CH4 in the atmosphere, it is expected that the SCA of CH4 will increase due to the increased removal of CH4 through a reaction with OH in the atmosphere. Spatially varying changes in the SCA could indicate long-term persistent variations in the seasonal sources and sinks, but such SCA changes have not been investigated. Here we use surface flask measurements and a 3D chemical transport model (TOMCAT) to diagnose changes in the SCA of atmospheric CH4 between 1995–2020 and attribute the changes regionally to contributions from different sectors. We find that the observed SCA decreased by 4 ppb (7.6 %) in the northern high latitudes (NHLs; 60–90∘ N), while the SCA increased globally by 2.5 ppb (6.5 %) during this time period. TOMCAT reproduces the change in the SCA at observation sites across the globe. Therefore, we use it to attribute regions which are contributing to the changes in the NHL SCA, which shows an unexpected change in the SCA that differs from the rest of the world. We find that well-mixed background CH4, likely from emissions originating in, and transported from, more southerly latitudes has the largest impact on the decreasing SCA in the NHLs (56.5 % of total contribution to NHLs). In addition to the background CH4, recent emissions from Canada, the Middle East, and Europe contribute 16.9 %, 12.1 %, and 8.4 %, respectively, to the total change in the SCA in the NHLs. The remaining contributions are due to changes in emissions and transport from other regions. The three largest regional contributions are driven by increases in summer emissions from the Boreal Plains in Canada, decreases in winter emissions across Europe, and a combination of increases in summer emissions and decreases in winter emissions over the Arabian Peninsula and Caspian Sea in the Middle East. These results highlight that changes in the observed seasonal cycle can be an indicator of changing emission regimes in local and non-local regions, particularly in the NHL, where the change is counterintuitive.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2023
    detail.hit.zdb_id: 2092549-9
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  • 8
    Online Resource
    Online Resource
    Copernicus GmbH ; 2018
    In:  Atmospheric Chemistry and Physics Vol. 18, No. 24 ( 2018-12-21), p. 18149-18168
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 18, No. 24 ( 2018-12-21), p. 18149-18168
    Abstract: Abstract. The atmospheric methane (CH4) growth rate has varied considerably in recent decades. Unexplained renewed growth after 2006 followed 7 years of stagnation and coincided with an isotopic trend toward CH4 more depleted in 13C, suggesting changes in sources and/or sinks. Using surface observations of both CH4 and the relative change of isotopologue ratio (δ13CH4) to constrain a global 3-D chemical transport model (CTM), we have performed a synthesis inversion for source and sink attribution. Our method extends on previous studies by providing monthly and regional attribution of emissions from six different sectors and changes in atmospheric sinks for the extended 2003–2015 period. Regional evaluation of the model CH4 tracer with independent column observations from the Greenhouse Gases Observing Satellite (GOSAT) shows improved performance when using posterior fluxes (R=0.94–0.96, RMSE =8.3–16.5 ppb), relative to prior fluxes (R=0.60–0.92, RMSE =48.6–64.6 ppb). Further independent validation with data from the Total Carbon Column Observing Network (TCCON) shows a similar improvement in the posterior fluxes (R=0.87, RMSE =18.8 ppb) compared to the prior fluxes (R=0.69, RMSE =55.9 ppb). Based on these improved posterior fluxes, the inversion results suggest the most likely cause of the renewed methane growth is a post-2007 1.8±0.4 % decrease in mean OH, a 12.9±2.7 % increase in energy sector emissions, mainly from Africa–Middle East and southern Asia–Oceania, and a 2.6±1.8 % increase in wetland emissions, mainly from northern Eurasia. The posterior wetland flux increases are in general agreement with bottom-up estimates, but the energy sector growth is greater than estimated by bottom-up methods. The model results are consistent across a range of sensitivity analyses. When forced to assume a constant (annually repeating) OH distribution, the inversion requires a greater increase in energy sector (13.6±2.7 %) and wetland (3.6±1.8 %) emissions and an 11.5±3.8 % decrease in biomass burning emissions. Assuming no prior trend in sources and sinks slightly reduces the posterior growth rate in energy sector and wetland emissions and further increases the magnitude of the negative OH trend. We find that possible tropospheric Cl variations do not influence δ13CH4 and CH4 trends, although we suggest further work on Cl variability is required to fully diagnose this contribution. While the study provides quantitative insight into possible emissions variations which may explain the observed trends, uncertainty in prior source and sink estimates and a paucity of δ13CH4 observations limit the robustness of the posterior estimates.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2018
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  • 9
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 21, No. 13 ( 2021-07-14), p. 10643-10669
    Abstract: Abstract. We use a global inverse model, satellite data and flask measurements to estimate methane (CH4) emissions from South America, Brazil and the basin of the Amazon River for the period 2010–2018. We find that emissions from Brazil have risen during this period, most quickly in the eastern Amazon basin, and that this is concurrent with increasing surface temperatures in this region. Brazilian CH4 emissions rose from 49.8 ± 5.4 Tg yr−1 in 2010–2013 to 55.6 ± 5.2 Tg yr−1 in 2014–2017, with the wet season of December–March having the largest positive trend in emissions. Amazon basin emissions grew from 41.7 ± 5.3 to 49.3 ± 5.1 Tg yr−1 during the same period. We derive no significant trend in regional emissions from fossil fuels during this period. We find that our posterior distribution of emissions within South America is significantly and consistently changed from our prior estimates, with the strongest emission sources being in the far north of the continent and to the south and south-east of the Amazon basin, at the mouth of the Amazon River and nearby marsh, swamp and mangrove regions. We derive particularly large emissions during the wet season of 2013/14, when flooding was prevalent over larger regions than normal within the Amazon basin. We compare our posterior CH4 mole fractions, derived from posterior fluxes, to independent observations of CH4 mole fraction taken at five lower- to mid-tropospheric vertical profiling sites over the Amazon and find that our posterior fluxes outperform prior fluxes at all locations. In particular the large emissions from the eastern Amazon basin are shown to be in good agreement with independent observations made at Santarém, a location which has long displayed higher mole fractions of atmospheric CH4 in contrast with other basin locations. We show that a bottom-up wetland flux model can match neither the variation in annual fluxes nor the positive trend in emissions produced by the inversion. Our results show that the Amazon alone was responsible for 24 ± 18 % of the total global increase in CH4 flux during the study period, and it may contribute further in future due to its sensitivity to temperature changes.
    Type of Medium: Online Resource
    ISSN: 1680-7324
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2021
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  • 10
    In: Biogeosciences, Copernicus GmbH, Vol. 17, No. 22 ( 2020-11-23), p. 5669-5691
    Abstract: Abstract. Wetland emissions contribute the largest uncertainties to the current global atmospheric CH4 budget, and how these emissions will change under future climate scenarios is also still poorly understood. Bloom et al. (2017b) developed WetCHARTs, a simple, data-driven, ensemble-based model that produces estimates of CH4 wetland emissions constrained by observations of precipitation and temperature. This study performs the first detailed global and regional evaluation of the WetCHARTs CH4 emission model ensemble against 9 years of high-quality, validated atmospheric CH4 observations from GOSAT (the Greenhouse Gases Observing Satellite). A 3-D chemical transport model is used to estimate atmospheric CH4 mixing ratios based on the WetCHARTs emissions and other sources. Across all years and all ensemble members, the observed global seasonal-cycle amplitude is typically underestimated by WetCHARTs by −7.4 ppb, but the correlation coefficient of 0.83 shows that the seasonality is well-produced at a global scale. The Southern Hemisphere has less of a bias (−1.9 ppb) than the Northern Hemisphere (−9.3 ppb), and our findings show that it is typically the North Tropics where this bias is the worst (−11.9 ppb). We find that WetCHARTs generally performs well in reproducing the observed wetland CH4 seasonal cycle for the majority of wetland regions although, for some regions, regardless of the ensemble configuration, WetCHARTs does not reproduce the observed seasonal cycle well. In order to investigate this, we performed detailed analysis of some of the more challenging exemplar regions (Paraná River, Congo, Sudd and Yucatán). Our results show that certain ensemble members are more suited to specific regions, due to either deficiencies in the underlying data driving the model or complexities in representing the processes involved. In particular, incorrect definition of the wetland extent is found to be the most common reason for the discrepancy between the modelled and observed CH4 concentrations. The remaining driving data (i.e. heterotrophic respiration and temperature) are shown to also contribute to the mismatch with observations, with the details differing on a region-by-region basis but generally showing that some degree of temperature dependency is better than none. We conclude that the data-driven approach used by WetCHARTs is well-suited to producing a benchmark ensemble dataset against which to evaluate more complex process-based land surface models that explicitly model the hydrological behaviour of these complex wetland regions.
    Type of Medium: Online Resource
    ISSN: 1726-4189
    Language: English
    Publisher: Copernicus GmbH
    Publication Date: 2020
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