scholarly journals Seasonal and interannual variability in wetland methane emissions simulated by CLM4Me' and CAM-chem and comparisons to observations of concentrations

2015 ◽  
Vol 12 (13) ◽  
pp. 4029-4049 ◽  
Author(s):  
L. Meng ◽  
R. Paudel ◽  
P. G. M. Hess ◽  
N. M. Mahowald

Abstract. Understanding the temporal and spatial variation of wetland methane emissions is essential to the estimation of the global methane budget. Our goal for this study is three-fold: (i) to evaluate the wetland methane fluxes simulated in two versions of the Community Land Model, the Carbon-Nitrogen (CN; i.e., CLM4.0) and the Biogeochemistry (BGC; i.e., CLM4.5) versions using the methane emission model CLM4Me' so as to determine the sensitivity of the emissions to the underlying carbon model; (ii) to compare the simulated atmospheric methane concentrations to observations, including latitudinal gradients and interannual variability so as to determine the extent to which the atmospheric observations constrain the emissions; (iii) to understand the drivers of seasonal and interannual variability in atmospheric methane concentrations. Simulations of the transport and removal of methane use the Community Atmosphere Model with chemistry (CAM-chem) model in conjunction with CLM4Me' methane emissions from both CN and BGC simulations and other methane emission sources from literature. In each case we compare model-simulated atmospheric methane concentration with observations. In addition, we simulate the atmospheric concentrations based on the TransCom wetland and rice paddy emissions derived from a different terrestrial ecosystem model, Vegetation Integrative Simulator for Trace gases (VISIT). Our analysis indicates CN wetland methane emissions are higher in the tropics and lower at high latitudes than emissions from BGC. In CN, methane emissions decrease from 1993 to 2004 while this trend does not appear in the BGC version. In the CN version, methane emission variations follow satellite-derived inundation wetlands closely. However, they are dissimilar in BGC due to its different carbon cycle. CAM-chem simulations with CLM4Me' methane emissions suggest that both prescribed anthropogenic and predicted wetlands methane emissions contribute substantially to seasonal and interannual variability in atmospheric methane concentration. Simulated atmospheric CH4 concentrations in CAM-chem are highly correlated with observations at most of the 14 measurement stations evaluated with an average correlation between 0.71 and 0.80 depending on the simulation (for the period of 1993–2004 for most stations based on data availability). Our results suggest that different spatial patterns of wetland emissions can have significant impacts on Northern and Southern hemisphere (N–S) atmospheric CH4 concentration gradients and growth rates. This study suggests that both anthropogenic and wetland emissions have significant contributions to seasonal and interannual variations in atmospheric CH4 concentrations. However, our analysis also indicates the existence of large uncertainties in terms of spatial patterns and magnitude of global wetland methane budgets, and that substantial uncertainty comes from the carbon model underlying the methane flux modules.

2015 ◽  
Vol 12 (3) ◽  
pp. 2161-2212 ◽  
Author(s):  
L. Meng ◽  
R. Paudel ◽  
P. G. M. Hess ◽  
N. M. Mahowald

Abstract. Understanding the temporal and spatial variation of wetland methane emissions is essential to the estimation of the global methane budget. We examine the seasonal and inter-annual variability in wetland methane emissions simulated in the Community Land Model (CLM4Me'). Methane emissions from both the Carbon-Nitrogen (CN, i.e. CLM4.0) and the Biogeochemistry (BGC, i.e. CLM4.5) versions of the CLM are evaluated. We further conduct simulations of the transport and removal of methane using the Community Atmosphere Model (CAM-chem) model using CLM4Me' methane emissions from both CN and BGC along with other methane sources and compare model simulated atmospheric methane concentration with observations. In addition, we simulate the atmospheric concentrations based on the TransCom wetland and rice paddy emissions from a different terrestrial ecosystem model VISIT. Our analysis suggests CN wetland methane emissions are higher in tropics and lower in high latitudes than BGC. In CN, methane emissions decrease from 1993 to 2004 while this trend does not appear in the BGC version. In the CN versions, methane emission variations follow satellite-derived inundation wetlands closely. However, they are dissimilar in BGC due to its different carbon cycle. CAM-chem model simulations with CLM4Me' methane emissions suggest that both prescribed anthropogenic and predicted wetlands methane emissions contribute substantially to seasonal and inter-annual variability in atmospheric methane concentration. It also suggests that different spatial patterns of wetland emissions can have significant impacts on N–S atmospheric CH4 concentration gradients and growth rates. This study suggests that large uncertainties still exist in terms of spatial patterns and magnitude of global wetland methane budgets, and that substantial uncertainty comes from the carbon model underlying the methane flux modules.


2015 ◽  
Vol 15 (1) ◽  
pp. 305-317 ◽  
Author(s):  
Z. M. Loh ◽  
R. M. Law ◽  
K. D. Haynes ◽  
P. B. Krummel ◽  
L. P. Steele ◽  
...  

Abstract. This study uses two climate models and six scenarios of prescribed methane emissions to compare modelled and observed atmospheric methane between 1994 and 2007, for Cape Grim, Australia (40.7° S, 144.7° E). The model simulations follow the TransCom-CH4 protocol and use the Australian Community Climate and Earth System Simulator (ACCESS) and the CSIRO Conformal-Cubic Atmospheric Model (CCAM). Radon is also simulated and used to reduce the impact of transport differences between the models and observations. Comparisons are made for air samples that have traversed the Australian continent. All six emission scenarios give modelled concentrations that are broadly consistent with those observed. There are three notable mismatches, however. Firstly, scenarios that incorporate interannually varying biomass burning emissions produce anomalously high methane concentrations at Cape Grim at times of large fire events in southeastern Australia, most likely due to the fire methane emissions being unrealistically input into the lowest model level. Secondly, scenarios with wetland methane emissions in the austral winter overestimate methane concentrations at Cape Grim during wintertime while scenarios without winter wetland emissions perform better. Finally, all scenarios fail to represent a~methane source in austral spring implied by the observations. It is possible that the timing of wetland emissions in the scenarios is incorrect with recent satellite measurements suggesting an austral spring (September–October–November), rather than winter, maximum for wetland emissions.


2021 ◽  
Author(s):  
Joannes Maasakkers ◽  
Daniel Varon ◽  
Aldís Elfarsdóttir ◽  
Jason McKeever ◽  
Dylan Jervis ◽  
...  

As atmospheric methane concentrations increase at record pace, it is critical to identify individual emission sources with high potential for mitigation. Landfills are responsible for large methane emissions that can be readily abated but have been sparsely observed. Here we leverage the synergy between satellite instruments with different spatiotemporal coverage and resolution to detect and quantify emissions from individual landfill facilities. We use the global surveying Tropospheric Monitoring Instrument (TROPOMI) to identify large emission hot spots, and then zoom in with high-resolution target-mode observations from the GHGSat instrument suite to identify the responsible facilities and characterize their emissions. Using this ‘tip and cue’ approach, we detect and analyze strongly emitting landfills (3-29 t hr−1) in Buenos Aires (Argentina), Delhi (India), Lahore (Pakistan), and Mumbai (India). We find that city-level emissions are 1.6-2.8 times larger than reported in commonly used emission inventories and that the landfills contribute 5-47% of those emissions. Our work demonstrates how complementary satellites enable global detection, identification, and monitoring of methane super-emitters at the facility-level.


The Holocene ◽  
2011 ◽  
Vol 21 (5) ◽  
pp. 735-741 ◽  
Author(s):  
Stephen J. Burns

Recent speleothem records from the tropics of both hemispheres document a gradual decrease in the intensity of the monsoons in the Northern Hemisphere and increase in the Southern Hemisphere monsoons over the Holocene. These changes are a direct response of the monsoons to precession-driven insolation variability. With regard to atmospheric methane, this shift should result in a decrease in Northern Hemisphere tropical methane emissions and increase in Southern Hemisphere emissions. It is plausible that that overall tropical methane production experienced a minimum in the mid-Holocene because of decreased seasonality in rainfall at the margins of the tropics. Changes in tropical methane production alone might, therefore, explain many of the characteristics of Holocene methane concentrations and isotopic chemistry.


2020 ◽  
Author(s):  
Ingeborg Bussmann ◽  
Irina Fedorova ◽  
Bennet Juhls ◽  
Pier Paul Overduin ◽  
Matthias Winkel

Abstract. Arctic regions and their water bodies are being affected by the most rapid climate warming on Earth. Arctic lakes and small ponds are known to act as an important source of atmospheric methane. However, not much is known about other types of water bodies in permafrost regions, which include major rivers and coastal bays as a transition type between freshwater and marine environments. We monitored dissolved methane concentrations in three different water bodies (Lena River, Tiksi Bay and Lake Golzovoye, Siberia, Russia) over a period of two years. Sampling was carried out under ice cover (April) and in open water (July/August). The methane oxidation (MOX) rate in water and melted ice samples from the late winter of 2017 was also investigated. In the Lena River winter methane concentrations were a quarter of the summer concentrations (8 vs 31 nmol L−1) and mean winter MOX rate was low (0.023 nmol L−1 d−1). In contrast, Tiksi Bay winter methane concentrations were 10-times higher than in summer (103 vs 13 nmol L−1). Winter MOX rates showed a median of 0.305 nmol L−1 d−1. In Lake Golzovoye, median methane concentrations in winter were 40-times higher than in summer (1957 vs 49 nmol L−1). However, MOX was much higher in the lake (2.95 nmol L−1 d−1) than in either the river or bay. The temperature had a strong influence on the MOX, (Q10 = 2.72 ± 0.69) compared to temperate environments. In the ice cores a median methane concentration of 9 nM was observed, with no gradient between the ice surface and the bottom layer at the ice-water-interface. MOX in the (melted) ice cores was mostly below the detection limit. Comparing methane concentrations in the ice with the underlaying water column revealed 100 – 1000-times higher methane concentration in the water column. The winter situation seemed to favor a methane accumulation under ice, especially in the lake with a stagnant water body. While on the other hand, in the Lena River with its flowing water no methane accumulation under ice was observed. Methane oxidation rate was not able to counteract this winter time accumulation.


2018 ◽  
Vol 15 (15) ◽  
pp. 4683-4709 ◽  
Author(s):  
Vivek K. Arora ◽  
Joe R. Melton ◽  
David Plummer

Abstract. Natural methane emissions from wetlands and fire, and soil uptake of methane, simulated using the Canadian Land Surface Scheme and Canadian Terrestrial Ecosystem (CLASS-CTEM) modelling framework, over the historical 1850–2008 period, are assessed by using a one-box model of atmospheric methane burden. This one-box model also requires anthropogenic emissions and the methane sink in the atmosphere to simulate the historical evolution of global methane burden. For this purpose, global anthropogenic methane emissions for the period 1850–2008 were reconstructed based on the harmonized representative concentration pathway (RCP) and Emission Database for Global Atmospheric Research (EDGAR) data sets. The methane sink in the atmosphere is represented using bias-corrected methane lifetimes from the Canadian Middle Atmosphere Model (CMAM). The resulting evolution of atmospheric methane concentration over the historical period compares reasonably well with observation-based estimates (correlation  =  0.99, root mean square error  =  35 ppb). The modelled natural emissions are also assessed using an inverse procedure where the methane lifetimes required to reproduce the observed year-to-year increase in atmospheric methane burden are calculated based upon the specified global anthropogenic and modelled natural emissions that we have used here. These calculated methane lifetimes over the historical period fall within the uncertainty range of observation-based estimates. The present-day (2000–2008) values of modelled methane emissions from wetlands (169 Tg CH4 yr−1) and fire (27 Tg CH4 yr−1), methane uptake by soil (29 Tg CH4 yr−1), and the budget terms associated with overall anthropogenic and natural emissions are consistent with estimates reported in a recent global methane budget that is based on top-down approaches constrained by observed atmospheric methane burden. The modelled wetland emissions increase over the historical period in response to both increases in precipitation and in atmospheric CO2 concentration. This increase in wetland emissions over the historical period yields evolution of the atmospheric methane concentration that compares better with observation-based values than the case when wetland emissions are held constant over the historical period.


2014 ◽  
Vol 119 (1) ◽  
pp. 24-34 ◽  
Author(s):  
Genevieve L. Noyce ◽  
Ruth K. Varner ◽  
Jill L. Bubier ◽  
Steve Frolking

2017 ◽  
Author(s):  
Vivek K. Arora ◽  
Joe R. Melton ◽  
David Plummer

Abstract. Natural methane emissions from wetlands and fire, and soil uptake of methane, simulated using the Canadian Land Surface Scheme and Canadian Terrestrial Ecosystem (CLASS-CTEM) modelling framework, over the historical 1850–2008 period, are assessed by using a one box model of atmospheric methane burden. This one box model also requires anthropogenic emissions and the methane sink in the atmosphere to simulate the historical evolution of global methane burden. For this purpose, global anthropogenic methane emissions for the period 1850-2008 were reconstructed based on the harmonized representative concentration pathway (RCP) and Emission Database for Global Atmospheric Research (EDGAR) data sets. The methane sink in the atmosphere is represented using bias-corrected methane lifetimes from the Canadian Middle Atmosphere Model (CMAM). The resulting evolution of atmospheric methane concentration over the historical period compares reasonably well with observation-based estimates. The modelled natural emissions are also assessed using an inverse procedure where the methane lifetimes required to reproduce the observed year-to-year increase in observed atmospheric methane burden are calculated based upon the global anthropogenic and modelled natural emissions that we have used here. These calculated methane lifetimes over the historical period fall within the uncertainty range of observation-based estimates. The present-day (2000–2008) values of modelled methane emissions from wetlands and fire, methane uptake by soil, and the budget terms associated with overall anthropogenic and natural emissions are consistent with estimates reported in a recent global methane budget that is based on top-down approaches constrained by observed atmospheric methane burden. The modelled wetland emissions increase over the historical period in response to both increase in precipitation and increase in atmospheric CO2 concentration. This increase in wetland emissions over the historical period yields evolution of the atmospheric methane concentration that compares better with observation-based values than the case when wetland emissions are held constant over the historical period.


Sign in / Sign up

Export Citation Format

Share Document