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Abstract Anthropogenic activities have substantially enhanced the loadings of reactive nitrogen (Nr) in the Earth system since pre-industrial times 1,2 , contributing to widespread eutrophication and air pollution 3–6 . Increased Nr can also influence global climate through a variety of effects on atmospheric and land processes but the cumulative net climate effect is yet to be unravelled. Here we show that anthropogenic Nr causes a net negative direct radiative forcing of −0.34 [−0.20, −0.50] W m −2 in the year 2019 relative to the year 1850. This net cooling effect is the result of increased aerosol loading, reduced methane lifetime and increased terrestrial carbon sequestration associated with increases in anthropogenic Nr, which are not offset by the warming effects of enhanced atmospheric nitrous oxide and ozone. Future predictions using three representative scenarios show that this cooling effect may be weakened primarily as a result of reduced aerosol loading and increased lifetime of methane, whereas in particular N 2 O-induced warming will probably continue to increase under all scenarios. Our results indicate that future reductions in anthropogenic Nr to achieve environmental protection goals need to be accompanied by enhanced efforts to reduce anthropogenic greenhouse gas emissions to achieve climate change mitigation in line with the Paris Agreement.

Abstract 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.

Abstract 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.

Abstract. Two interglacial epochs are included in the suite of Paleoclimate Modeling Intercomparison Project (PMIP4) simulations in the Coupled Model Intercomparison Project (CMIP6). The experimental protocols for simulations of the mid-Holocene (midHolocene, 6000 years before present) and the Last Interglacial (lig127k, 127 000 years before present) are described here. These equilibrium simulations are designed to examine the impact of changes in orbital forcing at times when atmospheric greenhouse gas levels were similar to those of the preindustrial period and the continental configurations were almost identical to modern ones. These simulations test our understanding of the interplay between radiative forcing and atmospheric circulation, and the connections among large-scale and regional climate changes giving rise to phenomena such as land–sea contrast and high-latitude amplification in temperature changes, and responses of the monsoons, as compared to today. They also provide an opportunity, through carefully designed additional sensitivity experiments, to quantify the strength of atmosphere, ocean, cryosphere, and land-surface feedbacks. Sensitivity experiments are proposed to investigate the role of freshwater forcing in triggering abrupt climate changes within interglacial epochs. These feedback experiments naturally lead to a focus on climate evolution during interglacial periods, which will be examined through transient experiments. Analyses of the sensitivity simulations will also focus on interactions between extratropical and tropical circulation, and the relationship between changes in mean climate state and climate variability on annual to multi-decadal timescales. The comparative abundance of paleoenvironmental data and of quantitative climate reconstructions for the Holocene and Last Interglacial make these two epochs ideal candidates for systematic evaluation of model performance, and such comparisons will shed new light on the importance of external feedbacks (e.g., vegetation, dust) and the ability of state-of-the-art models to simulate climate changes realistically.

Abstract 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.

Abstract 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.