reproducing methane distribution over the last decades with oslo ctm3
DESCRIPTION
Reproducing methane distribution over the last decades with Oslo CTM3. MOCA møte Oslo/Kjeller 29.10 2013 Stig B. Dalsøren. Overall objective “ Explain the recent increase in atmospheric methane and quantify the effect of realistic future methane levels” - PowerPoint PPT PresentationTRANSCRIPT
MOCA møte Oslo/Kjeller 29.10 2013Stig B. Dalsøren
Reproducing methane distribution over the last decades with Oslo CTM3
Overall objective “Explain the recent increase in atmospheric methane and quantify the effect of realistic future methane levels”
WP 1: Analysis of the historic level and development of methane
WP 2: Assessment of the recent development and current level of methane
WP 3: Future development of methane levels and corresponding climate impact
Global Chemical Transport model OsloCTM3
Figure from (Seinfeld and Pandis, 1998).
Vertical: 60 layersHorizontal:
T42: 2.8 x 2.8 degrees
(T159: 1.125 x 1.125 degrees)
Processes
Chemistry
Gas phase chemistry 90 species18 tracers, one for each methane emission sector
AerosolsSulphateSea saltNitrate(Black/organic carbon)(Mineral dust)(SOA) (not included in these simulations)
Anthropogenic methane emissions 1970-2008 from Edgar 4.2 database
19841985
19861987
19881989
19901991
19921993
19941995
19961997
19981999
20002001
20022003
20042005
20062007
20082009
0
50
100
150
200
250
WetlandsOceans+TermitesBBURTg
/yea
rNatural methane emissions 1984-2009 from Philippe Bousquet (Based on Bousquet et al. 2011)
Total methane emissions 1970-2012
Test runs using observed surface methane concentrations, comparing loss and emissions:
Year Emissions Loss (Tg)
2000 534.8 580
Assuming equilibrium between emissions and loss in 2000 results in the following scalingfactors of methane emissions:
Bousquet (biomass burning+natural): 1.1041Edgar 4.2 (anthropogenic): 1.0677:
-> New emissions used in model runs:
Year Emissions Loss (Tg)
2000 580 580
Scaling approach on methane emissions
Anthropogenic: 1970-2008 Edgar 4.2
Biomass burning: 1997-2011 GFED, all other years use GFED 2000
Natural: 2000 Megan, all other years use MEGAN 2000
Meteorology: 1997-2012, all other years use year 2000
Stratospheric concentrations ozone depleting substances: Strat 2d data introduced in runs from 1980 and onwards.
Non-methane emssions and other input data in simualtion
3 rather distinct periods in the level of sophitication of model runs
1970-1984: Kind of test/spinup. Only changes in anthropogenic emissions taken into account. Few methane measurements/no global network to compare with.
1984-1997: Variation also in methane emissions from biomass burning and natural sources. More methane observations to compare with
1997-2008: Variation also in non-methane biomass burning emissions and meteorology. Numerous methane observations to compare with.
Methane budget 1970-2012 in OsloCTM3
19701971
19721973
19741975
19761977
19781979
19801981
19821983
19841985
19861987
19881989
19901991
19921993
19941995
19961997
19981999
20002001
20022003
20042005
20062007
20082009
20102011
20121400
1450
1500
1550
1600
1650
1700
1750
1800
CTM3 Surface mean
Khalil et al. 1989
Blake and Rowland 1986
CTM3 surface mean BP
AGAGE
ppbv
Global average surface level from observations and OsloCTM3
Comparison observationsAvailable surface stations at WDCGG
" • " denotes that the data from the station has been updated in the last 365 days
Jan 2008
Jul 2008
Methane (ppbv) in lowest model layer in CTM3 compared to observations (circles)
Examples: Portion of comparisons for stations for the period 2003-2012
Stations: 30-90 S
Stations: 0-30 S
Stations: 0-30 N
Stations: 30-90 N
Months
ppbv
Days
ppbv
In line with isotope studies for selected periods during 2008 and 2009 (Fischer et al. (2011))
Arctic summer CH4 source in 2008 and 2009 was from wetlands. During winter time fossil gas emissions dominated the CH4 input. Submarine emissions along the West Spitsbergen slope was found to have negligible CH4 input to the atmosphere in summer, despite the fact that it was possible to identify methane bubbles in the sea from the sea floor. GAME project isotope instrument installed and measurements available since beginning of 2012.
Jan 2001- Oct 2012pp
bv ppbv
Days
OH influence on methane loss
Possible reasons that the model simulation has a larger growth rate for recent years than the observations:
Bergamschi et al 2013, inversion study:
“For all inversions, the derived overall trend of the anthropogenic emissions is smaller than the trend in the EDGARv4.2 emission inventory”
“Bousquet et al. 2011 attribute the increase in total emissionslargely to wetlands while in our study, a substantial fraction of the total increase is attributed to anthropogenic emissions»
Remaining work/future plans• A lot of material for further analysis .
- Further comparison surface observations- Further studies on methane tracers from the different emission sectors- Comparison satellites (IASI, Sciamachy,…) and vertical profiles ?
- Isotopes in OsloCTM3 ??
• More tests with different emissions for the period 2006/2009-2013 ??
- Test more assumptions on development natural and anthropogenic emissions after 2009 (period of lacking emission data in current simulations)
- Test further with hydrate emissions from ESS.
• Complete the «constant methane» simulation to reveal the effect of CO, NOx, NMVOC, Strat O3,...... changes on methane oxidation through OH.
• Setup and simulations with future realistic emission scenario(s) (WP 3 in GAME)
Solid fuels
Gas
OilWetlands
EnergyRice/soil
Enteric fermentation Biomass burning
Surface methane change (ppbv) 2006-2007