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  • 1
    In: Philosophical Transactions of the Royal Society B: Biological Sciences, The Royal Society, Vol. 373, No. 1760 ( 2018-11-19), p. 20170304-
    Kurzfassung: Evaluating the response of the land carbon sink to the anomalies in temperature and drought imposed by El Niño events provides insights into the present-day carbon cycle and its climate-driven variability. It is also a necessary step to build confidence in terrestrial ecosystems models' response to the warming and drying stresses expected in the future over many continents, and particularly in the tropics. Here we present an in-depth analysis of the response of the terrestrial carbon cycle to the 2015/2016 El Niño that imposed extreme warming and dry conditions in the tropics and other sensitive regions. First, we provide a synthesis of the spatio-temporal evolution of anomalies in net land–atmosphere CO 2 fluxes estimated by two in situ measurements based on atmospheric inversions and 16 land-surface models (LSMs) from TRENDYv6. Simulated changes in ecosystem productivity, decomposition rates and fire emissions are also investigated. Inversions and LSMs generally agree on the decrease and subsequent recovery of the land sink in response to the onset, peak and demise of El Niño conditions and point to the decreased strength of the land carbon sink: by 0.4–0.7 PgC yr −1 (inversions) and by 1.0 PgC yr −1 (LSMs) during 2015/2016. LSM simulations indicate that a decrease in productivity, rather than increase in respiration, dominated the net biome productivity anomalies in response to ENSO throughout the tropics, mainly associated with prolonged drought conditions. This article is part of a discussion meeting issue ‘The impact of the 2015/2016 El Niño on the terrestrial tropical carbon cycle: patterns, mechanisms and implications’.
    Materialart: Online-Ressource
    ISSN: 0962-8436 , 1471-2970
    RVK:
    Sprache: Englisch
    Verlag: The Royal Society
    Publikationsdatum: 2018
    ZDB Id: 1462620-2
    SSG: 12
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  • 2
    In: Earth System Dynamics, Copernicus GmbH, Vol. 14, No. 4 ( 2023-08-14), p. 767-795
    Kurzfassung: Abstract. Terrestrial carbon (C) sequestration is limited by nitrogen (N), an empirically established constraint that could intensify under CO2 fertilization and future global change. The terrestrial C sink is estimated to currently sequester approximately a third of annual anthropogenic CO2 emissions based on an ensemble of terrestrial biosphere models, which have been evaluated in their ability to reproduce observations of the C, water, and energy cycles. However, their ability to reproduce observations of N cycling and thus the regulation of terrestrial C sequestration by N have been largely unexplored. Here, we evaluate an ensemble of terrestrial biosphere models with coupled C–N cycling and their performance at simulating N cycling, outlining a framework for evaluating N cycling that can be applied across terrestrial biosphere models. We find that models exhibit significant variability across N pools and fluxes, simulating different magnitudes and trends over the historical period, despite their ability to generally reproduce the historical terrestrial C sink. Furthermore, there are no significant correlations between model performance in simulating N cycling and model performance in simulating C cycling, nor are there significant differences in model performance between models with different representations of fundamental N cycling processes. This suggests that the underlying N processes that regulate terrestrial C sequestration operate differently across models and appear to be disconnected from C cycling. Models tend to overestimate tropical biological N fixation, vegetation C : N ratio, and soil C : N ratio but underestimate temperate biological N fixation relative to observations. However, there is significant uncertainty associated with measurements of N cycling processes given their scarcity (especially relative to those of C cycling processes) and their high spatiotemporal variability. Overall, our results suggest that terrestrial biosphere models that represent coupled C–N cycling could be overestimating C storage per unit N, which could lead to biases in projections of the future terrestrial C sink under CO2 fertilization and future global change (let alone those without a representation of N cycling). More extensive observations of N cycling processes and comparisons against experimental manipulations are crucial to evaluate N cycling and its impact on C cycling and guide its development in terrestrial biosphere models.
    Materialart: Online-Ressource
    ISSN: 2190-4987
    Sprache: Englisch
    Verlag: Copernicus GmbH
    Publikationsdatum: 2023
    ZDB Id: 2578793-7
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  • 3
    In: Nature, Springer Science and Business Media LLC, Vol. 586, No. 7828 ( 2020-10-08), p. 248-256
    Materialart: Online-Ressource
    ISSN: 0028-0836 , 1476-4687
    RVK:
    RVK:
    RVK:
    Sprache: Englisch
    Verlag: Springer Science and Business Media LLC
    Publikationsdatum: 2020
    ZDB Id: 120714-3
    ZDB Id: 1413423-8
    SSG: 11
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  • 4
    In: Earth System Science Data, Copernicus GmbH, Vol. 8, No. 2 ( 2016-12-12), p. 697-751
    Kurzfassung: Abstract. The global methane (CH4) budget is becoming an increasingly important component for managing realistic pathways to mitigate climate change. This relevance, due to a shorter atmospheric lifetime and a stronger warming potential than carbon dioxide, is challenged by the still unexplained changes of atmospheric CH4 over the past decade. Emissions and concentrations of CH4 are continuing to increase, making CH4 the second most important human-induced greenhouse gas after carbon dioxide. Two major difficulties in reducing uncertainties come from the large variety of diffusive CH4 sources that overlap geographically, and from the destruction of CH4 by the very short-lived hydroxyl radical (OH). To address these difficulties, we have established a consortium of multi-disciplinary scientists under the umbrella of the Global Carbon Project to synthesize and stimulate research on the methane cycle, and producing regular (∼ biennial) updates of the global methane budget. This consortium includes atmospheric physicists and chemists, biogeochemists of surface and marine emissions, and socio-economists who study anthropogenic emissions. Following Kirschke et al. (2013), we propose here the first version of a living review paper that integrates results of top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up models, inventories and data-driven approaches (including process-based models for estimating land surface emissions and atmospheric chemistry, and inventories for anthropogenic emissions, data-driven extrapolations). For the 2003–2012 decade, global methane emissions are estimated by top-down inversions at 558 Tg CH4 yr−1, range 540–568. About 60 % of global emissions are anthropogenic (range 50–65 %). Since 2010, the bottom-up global emission inventories have been closer to methane emissions in the most carbon-intensive Representative Concentrations Pathway (RCP8.5) and higher than all other RCP scenarios. Bottom-up approaches suggest larger global emissions (736 Tg CH4 yr−1, range 596–884) mostly because of larger natural emissions from individual sources such as inland waters, natural wetlands and geological sources. Considering the atmospheric constraints on the top-down budget, it is likely that some of the individual emissions reported by the bottom-up approaches are overestimated, leading to too large global emissions. Latitudinal data from top-down emissions indicate a predominance of tropical emissions (∼ 64 % of the global budget, 〈 30° N) as compared to mid (∼ 32 %, 30–60° N) and high northern latitudes (∼ 4 %, 60–90° N). Top-down inversions consistently infer lower emissions in China (∼ 58 Tg CH4 yr−1, range 51–72, −14 %) and higher emissions in Africa (86 Tg CH4 yr−1, range 73–108, +19 %) than bottom-up values used as prior estimates. Overall, uncertainties for anthropogenic emissions appear smaller than those from natural sources, and the uncertainties on source categories appear larger for top-down inversions than for bottom-up inventories and models. The most important source of uncertainty on the methane budget is attributable to emissions from wetland and other inland waters. We show that the wetland extent could contribute 30–40 % on the estimated range for wetland emissions. Other priorities for improving the methane budget include the following: (i) the development of process-based models for inland-water emissions, (ii) the intensification of methane observations at local scale (flux measurements) to constrain bottom-up land surface models, and at regional scale (surface networks and satellites) to constrain top-down inversions, (iii) improvements in the estimation of atmospheric loss by OH, and (iv) improvements of the transport models integrated in top-down inversions. The data presented here can be downloaded from the Carbon Dioxide Information Analysis Center (http://doi.org/10.3334/CDIAC/GLOBAL_METHANE_BUDGET_2016_V1.1) and the Global Carbon Project.
    Materialart: Online-Ressource
    ISSN: 1866-3516
    Sprache: Englisch
    Verlag: Copernicus GmbH
    Publikationsdatum: 2016
    ZDB Id: 2475469-9
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  • 5
    In: Atmospheric Chemistry and Physics, Copernicus GmbH, Vol. 17, No. 18 ( 2017-09-20), p. 11135-11161
    Kurzfassung: Abstract. Following the recent Global Carbon Project (GCP) synthesis of the decadal methane (CH4) budget over 2000–2012 (Saunois et al., 2016), we analyse here the same dataset with a focus on quasi-decadal and inter-annual variability in CH4 emissions. The GCP dataset integrates results from top-down studies (exploiting atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up models (including process-based models for estimating land surface emissions and atmospheric chemistry), inventories of anthropogenic emissions, and data-driven approaches. The annual global methane emissions from top-down studies, which by construction match the observed methane growth rate within their uncertainties, all show an increase in total methane emissions over the period 2000–2012, but this increase is not linear over the 13 years. Despite differences between individual studies, the mean emission anomaly of the top-down ensemble shows no significant trend in total methane emissions over the period 2000–2006, during the plateau of atmospheric methane mole fractions, and also over the period 2008–2012, during the renewed atmospheric methane increase. However, the top-down ensemble mean produces an emission shift between 2006 and 2008, leading to 22 [16–32] Tg CH4 yr−1 higher methane emissions over the period 2008–2012 compared to 2002–2006. This emission increase mostly originated from the tropics, with a smaller contribution from mid-latitudes and no significant change from boreal regions. The regional contributions remain uncertain in top-down studies. Tropical South America and South and East Asia seem to contribute the most to the emission increase in the tropics. However, these two regions have only limited atmospheric measurements and remain therefore poorly constrained. The sectorial partitioning of this emission increase between the periods 2002–2006 and 2008–2012 differs from one atmospheric inversion study to another. However, all top-down studies suggest smaller changes in fossil fuel emissions (from oil, gas, and coal industries) compared to the mean of the bottom-up inventories included in this study. This difference is partly driven by a smaller emission change in China from the top-down studies compared to the estimate in the Emission Database for Global Atmospheric Research (EDGARv4.2) inventory, which should be revised to smaller values in a near future. We apply isotopic signatures to the emission changes estimated for individual studies based on five emission sectors and find that for six individual top-down studies (out of eight) the average isotopic signature of the emission changes is not consistent with the observed change in atmospheric 13CH4. However, the partitioning in emission change derived from the ensemble mean is consistent with this isotopic constraint. At the global scale, the top-down ensemble mean suggests that the dominant contribution to the resumed atmospheric CH4 growth after 2006 comes from microbial sources (more from agriculture and waste sectors than from natural wetlands), with an uncertain but smaller contribution from fossil CH4 emissions. In addition, a decrease in biomass burning emissions (in agreement with the biomass burning emission databases) makes the balance of sources consistent with atmospheric 13CH4 observations. In most of the top-down studies included here, OH concentrations are considered constant over the years (seasonal variations but without any inter-annual variability). As a result, the methane loss (in particular through OH oxidation) varies mainly through the change in methane concentrations and not its oxidants. For these reasons, changes in the methane loss could not be properly investigated in this study, although it may play a significant role in the recent atmospheric methane changes as briefly discussed at the end of the paper.
    Materialart: Online-Ressource
    ISSN: 1680-7324
    Sprache: Englisch
    Verlag: Copernicus GmbH
    Publikationsdatum: 2017
    ZDB Id: 2092549-9
    ZDB Id: 2069847-1
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  • 6
    In: Earth System Science Data, Copernicus GmbH, Vol. 12, No. 3 ( 2020-07-15), p. 1561-1623
    Kurzfassung: Abstract. Understanding and quantifying the global methane (CH4) budget is important for assessing realistic pathways to mitigate climate change. Atmospheric emissions and concentrations of CH4 continue to increase, making CH4 the second most important human-influenced greenhouse gas in terms of climate forcing, after carbon dioxide (CO2). The relative importance of CH4 compared to CO2 depends on its shorter atmospheric lifetime, stronger warming potential, and variations in atmospheric growth rate over the past decade, the causes of which are still debated. Two major challenges in reducing uncertainties in the atmospheric growth rate arise from the variety of geographically overlapping CH4 sources and from the destruction of CH4 by short-lived hydroxyl radicals (OH). To address these challenges, we have established a consortium of multidisciplinary scientists under the umbrella of the Global Carbon Project to synthesize and stimulate new research aimed at improving and regularly updating the global methane budget. Following Saunois et al. (2016), we present here the second version of the living review paper dedicated to the decadal methane budget, integrating results of top-down studies (atmospheric observations within an atmospheric inverse-modelling framework) and bottom-up estimates (including process-based models for estimating land surface emissions and atmospheric chemistry, inventories of anthropogenic emissions, and data-driven extrapolations). For the 2008–2017 decade, global methane emissions are estimated by atmospheric inversions (a top-down approach) to be 576 Tg CH4 yr−1 (range 550–594, corresponding to the minimum and maximum estimates of the model ensemble). Of this total, 359 Tg CH4 yr−1 or ∼ 60 % is attributed to anthropogenic sources, that is emissions caused by direct human activity (i.e. anthropogenic emissions; range 336–376 Tg CH4 yr−1 or 50 %–65 %). The mean annual total emission for the new decade (2008–2017) is 29 Tg CH4 yr−1 larger than our estimate for the previous decade (2000–2009), and 24 Tg CH4 yr−1 larger than the one reported in the previous budget for 2003–2012 (Saunois et al., 2016). Since 2012, global CH4 emissions have been tracking the warmest scenarios assessed by the Intergovernmental Panel on Climate Change. Bottom-up methods suggest almost 30 % larger global emissions (737 Tg CH4 yr−1, range 594–881) than top-down inversion methods. Indeed, bottom-up estimates for natural sources such as natural wetlands, other inland water systems, and geological sources are higher than top-down estimates. The atmospheric constraints on the top-down budget suggest that at least some of these bottom-up emissions are overestimated. The latitudinal distribution of atmospheric observation-based emissions indicates a predominance of tropical emissions (∼ 65 % of the global budget, 〈 30∘ N) compared to mid-latitudes (∼ 30 %, 30–60∘ N) and high northern latitudes (∼ 4 %, 60–90∘ N). The most important source of uncertainty in the methane budget is attributable to natural emissions, especially those from wetlands and other inland waters. Some of our global source estimates are smaller than those in previously published budgets (Saunois et al., 2016; Kirschke et al., 2013). In particular wetland emissions are about 35 Tg CH4 yr−1 lower due to improved partition wetlands and other inland waters. Emissions from geological sources and wild animals are also found to be smaller by 7 Tg CH4 yr−1 by 8 Tg CH4 yr−1, respectively. However, the overall discrepancy between bottom-up and top-down estimates has been reduced by only 5 % compared to Saunois et al. (2016), due to a higher estimate of emissions from inland waters, highlighting the need for more detailed research on emissions factors. Priorities for improving the methane budget include (i) a global, high-resolution map of water-saturated soils and inundated areas emitting methane based on a robust classification of different types of emitting habitats; (ii) further development of process-based models for inland-water emissions; (iii) intensification of methane observations at local scales (e.g., FLUXNET-CH4 measurements) and urban-scale monitoring to constrain bottom-up land surface models, and at regional scales (surface networks and satellites) to constrain atmospheric inversions; (iv) improvements of transport models and the representation of photochemical sinks in top-down inversions; and (v) development of a 3D variational inversion system using isotopic and/or co-emitted species such as ethane to improve source partitioning. The data presented here can be downloaded from https://doi.org/10.18160/GCP-CH4-2019 (Saunois et al., 2020) and from the Global Carbon Project.
    Materialart: Online-Ressource
    ISSN: 1866-3516
    Sprache: Englisch
    Verlag: Copernicus GmbH
    Publikationsdatum: 2020
    ZDB Id: 2475469-9
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  • 7
    In: Environmental Research Letters, IOP Publishing, Vol. 12, No. 9 ( 2017-09-01), p. 094013-
    Kurzfassung: Increasing atmospheric methane (CH 4 ) concentrations have contributed to approximately 20% of anthropogenic climate change. Despite the importance of CH 4 as a greenhouse gas, its atmospheric growth rate and dynamics over the past two decades, which include a stabilization period (1999–2006), followed by renewed growth starting in 2007, remain poorly understood. We provide an updated estimate of CH 4 emissions from wetlands, the largest natural global CH 4 source, for 2000–2012 using an ensemble of biogeochemical models constrained with remote sensing surface inundation and inventory-based wetland area data. Between 2000–2012, boreal wetland CH 4 emissions increased by 1.2 Tg yr −1 (−0.2–3.5 Tg yr −1 ), tropical emissions decreased by 0.9 Tg yr −1 (−3.2−1.1 Tg yr −1 ), yet globally, emissions remained unchanged at 184 ± 22 Tg yr −1 . Changing air temperature was responsible for increasing high-latitude emissions whereas declines in low-latitude wetland area decreased tropical emissions; both dynamics are consistent with features of predicted centennial-scale climate change impacts on wetland CH 4 emissions. Despite uncertainties in wetland area mapping, our study shows that global wetland CH 4 emissions have not contributed significantly to the period of renewed atmospheric CH 4 growth, and is consistent with findings from studies that indicate some combination of increasing fossil fuel and agriculture-related CH 4 emissions, and a decrease in the atmospheric oxidative sink.
    Materialart: Online-Ressource
    ISSN: 1748-9326
    Sprache: Unbekannt
    Verlag: IOP Publishing
    Publikationsdatum: 2017
    ZDB Id: 2255379-4
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  • 8
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    American Meteorological Society ; 2018
    In:  Bulletin of the American Meteorological Society Vol. 99, No. 6 ( 2018-06), p. 1231-1251
    In: Bulletin of the American Meteorological Society, American Meteorological Society, Vol. 99, No. 6 ( 2018-06), p. 1231-1251
    Kurzfassung: Nitrous oxide (N 2 O) is an important greenhouse gas and also an ozone-depleting substance that has both natural and anthropogenic sources. Large estimation uncertainty remains on the magnitude and spatiotemporal patterns of N 2 O fluxes and the key drivers of N 2 O production in the terrestrial biosphere. Some terrestrial biosphere models have been evolved to account for nitrogen processes and to show the capability to simulate N 2 O emissions from land ecosystems at the global scale, but large discrepancies exist among their estimates primarily because of inconsistent input datasets, simulation protocol, and model structure and parameterization schemes. Based on the consistent model input data and simulation protocol, the global N 2 O Model Intercomparison Project (NMIP) was initialized with 10 state-of-the-art terrestrial biosphere models that include nitrogen (N) cycling. Specific objectives of NMIP are to 1) unravel the major N cycling processes controlling N 2 O fluxes in each model and identify the uncertainty sources from model structure, input data, and parameters; 2) quantify the magnitude and spatial and temporal patterns of global and regional N 2 O fluxes from the preindustrial period (1860) to present and attribute the relative contributions of multiple environmental factors to N 2 O dynamics; and 3) provide a benchmarking estimate of N 2 O fluxes through synthesizing the multimodel simulation results and existing estimates from ground-based observations, inventories, and statistical and empirical extrapolations. This study provides detailed descriptions for the NMIP protocol, input data, model structure, and key parameters, along with preliminary simulation results. The global and regional N 2 O estimation derived from the NMIP is a key component of the global N 2 O budget synthesis activity jointly led by the Global Carbon Project and the International Nitrogen Initiative.
    Materialart: Online-Ressource
    ISSN: 0003-0007 , 1520-0477
    Sprache: Unbekannt
    Verlag: American Meteorological Society
    Publikationsdatum: 2018
    ZDB Id: 2029396-3
    ZDB Id: 419957-1
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  • 9
    In: Global Change Biology, Wiley, Vol. 29, No. 15 ( 2023-08), p. 4298-4312
    Kurzfassung: The recent rise in atmospheric methane (CH 4 ) concentrations accelerates climate change and offsets mitigation efforts. Although wetlands are the largest natural CH 4 source, estimates of global wetland CH 4 emissions vary widely among approaches taken by bottom‐up (BU) process‐based biogeochemical models and top‐down (TD) atmospheric inversion methods. Here, we integrate in situ measurements, multi‐model ensembles, and a machine learning upscaling product into the International Land Model Benchmarking system to examine the relationship between wetland CH 4 emission estimates and model performance. We find that using better‐performing models identified by observational constraints reduces the spread of wetland CH 4 emission estimates by 62% and 39% for BU‐ and TD‐based approaches, respectively. However, global BU and TD CH 4 emission estimate discrepancies increased by about 15% (from 31 to 36 TgCH 4 year −1 ) when the top 20% models were used, although we consider this result moderately uncertain given the unevenly distributed global observations. Our analyses demonstrate that model performance ranking is subject to benchmark selection due to large inter‐site variability, highlighting the importance of expanding coverage of benchmark sites to diverse environmental conditions. We encourage future development of wetland CH 4 models to move beyond static benchmarking and focus on evaluating site‐specific and ecosystem‐specific variabilities inferred from observations.
    Materialart: Online-Ressource
    ISSN: 1354-1013 , 1365-2486
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2023
    ZDB Id: 2020313-5
    SSG: 12
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  • 10
    In: Global Change Biology, Wiley, Vol. 25, No. 2 ( 2019-02), p. 640-659
    Kurzfassung: Our understanding and quantification of global soil nitrous oxide (N 2 O) emissions and the underlying processes remain largely uncertain. Here, we assessed the effects of multiple anthropogenic and natural factors, including nitrogen fertilizer (N) application, atmospheric N deposition, manure N application, land cover change, climate change, and rising atmospheric CO 2 concentration, on global soil N 2 O emissions for the period 1861–2016 using a standard simulation protocol with seven process‐based terrestrial biosphere models. Results suggest global soil N 2 O emissions have increased from 6.3 ± 1.1 Tg N 2 O‐N/year in the preindustrial period (the 1860s) to 10.0 ± 2.0 Tg N 2 O‐N/year in the recent decade (2007–2016). Cropland soil emissions increased from 0.3 Tg N 2 O‐N/year to 3.3 Tg N 2 O‐N/year over the same period, accounting for 82% of the total increase. Regionally, China, South Asia, and Southeast Asia underwent rapid increases in cropland N 2 O emissions since the 1970s. However, US cropland N 2 O emissions had been relatively flat in magnitude since the 1980s, and EU cropland N 2 O emissions appear to have decreased by 14%. Soil N 2 O emissions from predominantly natural ecosystems accounted for 67% of the global soil emissions in the recent decade but showed only a relatively small increase of 0.7 ± 0.5 Tg N 2 O‐N/year (11%) since the 1860s. In the recent decade, N fertilizer application, N deposition, manure N application, and climate change contributed 54%, 26%, 15%, and 24%, respectively, to the total increase. Rising atmospheric CO 2 concentration reduced soil N 2 O emissions by 10% through the enhanced plant N uptake, while land cover change played a minor role. Our estimation here does not account for indirect emissions from soils and the directed emissions from excreta of grazing livestock. To address uncertainties in estimating regional and global soil N 2 O emissions, this study recommends several critical strategies for improving the process‐based simulations.
    Materialart: Online-Ressource
    ISSN: 1354-1013 , 1365-2486
    URL: Issue
    Sprache: Englisch
    Verlag: Wiley
    Publikationsdatum: 2019
    ZDB Id: 2020313-5
    SSG: 12
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