Recent and future trends in atmospheric methane: Connecting global chemistry, climate and ozone pollution Arlene M.
Download ReportTranscript Recent and future trends in atmospheric methane: Connecting global chemistry, climate and ozone pollution Arlene M.
Recent and future trends in atmospheric methane: Connecting global chemistry, climate and ozone pollution Arlene M. Fiore ([email protected]) Acknowledgments: Larry Horowitz, Chip Levy (NOAA/GFDL) Jason West, Vaishali Naik (Princeton University) Ellen Baum, Joe Chaisson (Clean Air Task Force) Funding from Luce Foundation via Clean Air Task Force Berkeley Atmospheric Sciences Symposium, September 29, 2006 Historical increase in atmospheric methane and ozone Variations of CH4 Concentration (ppb) Over the Past 1000 years [Etheridge et al., 1998] Ozone at European mountain sites 1870-1990 [Marenco et al., 1994] 1600 1400 1200 1000 800 1000 1500 Year 2000 Radiative forcing of climate, 1750-Present: Important contributions from methane and ozone IPCC [2001] Level of scientific understanding Air quality-Climate Linkage: CH4, O3 are important greenhouse gases CH4 contributes to background O3 in surface air Free Troposphere hn O3 NO2 NO OH HO2 Global Background O3 Direct Intercontinental Transport Boundary layer (0-3 km) VOC, CH4, CO NOx NMVOCs CONTINENT 1 air pollution (smog) O3 air pollution (smog) OCEAN NOx NMVOCs CONTINENT 2 O3 IPCC [2001] scenarios project future growth Projections of future CH4 emissions (Tg CH4) to 2100 Change in 10-model mean surface O3 2100 SRES A2 - 2000 Attributed mainly to increases in methane and NOx [Prather et al., 2003] Ozone abatement strategies evolve as our understanding of the ozone problem advances O3 smog recognized as an URBAN problem: Los Angeles, Haagen-Smit identifies chemical mechanism Smog as REGIONAL problem; role of NOx and biogenic VOCs recognized 1950s Abatement Strategy: NMVOCs A GLOBAL perspective: role of intercontinental transport, background Present 1980s + NOx + CH4?? “Methane (and CO) emission control is an effective way of simultaneously meeting air quality standards and abating global warming” --- EMEP/CCC-Report 1/2005 Impacts of O3 precursor reductions on U.S. summer afternoon surface O3 frequency distributions GEOS-Chem Model Simulations (4°x5°) NOx controls strongly decrease the highest O3 (regional pollution episodes) CH4 controls affect the entire O3 distribution similarly (background) Results add linearly when both methane and NOx are reduced Fiore et al., 2002; West & Fiore, ES&T, 2005 Rising background O3 has implications for attaining air quality standards Surface O3 background appears to be rising [e.g. Lin et al., 2000; Jaffe et al., 2003, 2005; Vingarzan, 2004; EMEP/CCC-Report 1/2005 ] Pre-industrial background 20 Europe seasonal 40 Current background Future background? WHO/Europe 8-hr average 60 U.S. 8-hr average 80 100 O3 (ppbv) Methane trends and linkages with chemistry, climate, and ozone pollution 1) Methane Trends from 1990 to 2004 Are emission inventories consistent with observed CH4 trends? Role of changing sources? Role of changing sinks? 2) Climate and air quality benefits from CH4 controls Characterize the ozone response to CH4 control Compare with traditional controls on NOx, NMVOC Incorporate methane controls into a future emission scenario Research Tool: MOZART-2 Global Chemical Transport Model [Horowitz et al., 2003] NCEP, 1.9°x1.9°, 28 vertical levels Fully represent methane-OH relationship Test directly with observations 3D model structure More than half of global methane emissions are influenced by human activities ~300 Tg CH4 yr-1 Anthropogenic [EDGAR 3.2 Fast-Track 2000; Olivier et al., 2005] ~200 Tg CH4 yr-1 Biogenic sources [Wang et al., 2004] >25% uncertainty in total emissions Clathrates? Melting permafrost? PLANTS? BIOMASS BURNING + BIOFUEL ANIMALS 30 WETLANDS 90 180 60-240 Keppler et al., 2006 85 Sanderson et al., 2006 10-60 Kirschbaum et al., 2006 0-46 Ferretti et al., 2006 GLOBAL METHANE SOURCES (Tg CH4 yr-1) TERMITES RICE 40 20 COAL 30 LANDFILLS + WASTEWATER 50 GAS + OIL 60 Observed trend in surface CH4 (ppb) 1990-2004 Global Mean CH4 (ppb) Hypotheses for leveling off discussed in the literature: 1790 1780 1. Approach to steady-state 1770 1760 NOAA GMD Network 1750 1740 1730 1720 2. Source Changes Anthropogenic Wetlands/plants (Biomass burning) 3. (Transport) 1710 1990 1992 1994 1996 1998 2000 2002 2004 Data from 42 GMD stations with 8-yr minimum record is area-weighted, after averaging in bands 60-90N, 30-60N, 0-30N, 0-30S, 30-90S 4. Sink (CH4+OH) Humidity Temperature OH precursor emissions overhead O3 columns Can the model capture the observed trend (and be used for attribution)? BASE simulation EDGAR 2.0 emissions held constant 1790 1780 Global Mean Surface Methane (ppb) OBSERVED MOZART-2 1770 1760 Mean Bias (ppb) Bias and correlation vs. observed surface CH4: 1990-2004 Overestimates interhemispheric gradient 1750 1740 1730 1720 1990 1992 1994 1996 1998 2000 2002 2004 Overestimates 1990-1997 but matches trend Captures flattening post1998 but underestimates abundance r2 1710 Correlates poorly at high N latitudes S Latitude N Biomass Burning Ruminants Estimates for changing methane sources in the 1990s Rice Biogenic Wastewater Inter-annually varying wetland emissions Biomass Burning Landfills 1990-1998 from Wang et al. [2004] Ruminants Energy (Tg CH4 yr-1); different distribution Rice Biogenic adjusted to maintain 270 constant total source Wastewater 260 Landfills 547 Energy 1995 500v3.2 2000 v3.2 250 Tg CH4 yr-1 240 Biogenic 230 Biomass Burning Ruminants 220 Rice 210 Wastewater Landfills 200 Energy 1990 1995 400 300 200 100 2000 Apply climatological mean (224 Tg yr-1) post-1998 0 1990 v2.0 1990 v3.2 1995 v3.2 2000 v3.2 BASE ANTH EDGAR anthropogenic inventory ANTH + BIO 2005 Bias & Correlation vs. GMD CH4 observations: 1990-2004 Global Mean Surface Methane (ppb) Mean Bias (ppb) 1790 1780 1770 1760 1750 OBS BASE ANTH 1740 1730 1720 1710 1990 1992 1994 1996 1998 2000 2002 2004 ANTH simulation with time-varying EDGAR 3.2 emissions: Improves abundance post-1998 Interhemispheric gradient too high Poor correlation at high N latitudes r2 S Latitude N Bias & Correlation vs. GMD CH4 observations: 1990-2004 Global Mean Surface Methane (ppb) Mean Bias (ppb) 1790 1780 1770 1760 1750 OBS BASE ANTH ANTH+BIO 1740 1730 1720 1710 1990 1995 2000 2005 ANTH+BIO simulation with timevarying EDGAR 3.2 + wetland emissions improves: Global mean surface conc. Interhemispheric gradient Correlation at high N latitudes Fiore et al., GRL, 2006 r2 S Latitude N How does meteorology influence methane abundances? Why does BASE run with constant emissions level off post-1998? Examine sink CH4 Lifetime (t) against Tropospheric OH t= [CH 4 ] k[OH][CH 4 ] Dt Temperature (88% of CH4 loss is below 500 hPa ) Humidity Photolysis Lightning NOx Dt = 0.17 yr = 1.6%) What drives the change in methane lifetime in the model? Small increases in temperature and OH shorten the methane lifetime against tropospheric OH DtOH 0.18 Deconstruct Dt (-0.17 years) from 1991-1995 to 2000-2004 into individual contributions by varying OH and temperature separately 0.16 0.14 0.12 0.1 0.08 + 0.06 = 0.04 0.02 Lightning NOx 3.4 Global Lightning NOx (TgN yr-1) 0 DT(+0.3K) climT DOH(+1.2%) climOH BASE BASE 3.2 LNOx (TgN/y) 3 2.8 An increase in lightning NOx drives the OH increase in the model 2.6 2.4 2.2 But lightning NOx is highly parameterized …how robust is this result? 2 1.8 1990 1992 1994 1996 1998 Year 2000 2002 2004 Work in progress: Additional evidence for a global lightning NOx increase? Estimate lightning NOx changes using options available in the GFDL Atmospheric General Circulation Model: • Convection schemes (RAS vs. Donner-deep) • Meteorology (free-running vs. nudged to NCEP reanalysis) Lightning NOx NOx change, 1991-95 to 2000-04 Lightning change, 1991-95 to 2000-04 20% 20% Lightning NOx % change (91-95 to 00-04) RAS Donner MOZART 18% 18% More physically-based lightning NOx scheme [Petersen et al., 2005] 16% 16% Evidence from observations? 14% 14% MOZART-2 MOZART-2 10% 10% AM2 AM2 % change 12% 12% 8% 8% 6% 6% 4% 4% 2% 2% 0% 0% AM2-D AM2-D NCEP(nudged) free-running GCM Lightning NOx increase robust; magnitude depends on meteorology c/o L.W. Horowitz LIS/OTD Flash counts Magnetic field variations in the lower ELF range [e.g. Williams, 1992; Füllekrug and FraserSmith, 1997; Price, 2000] Negev Desert Station, Israel Recap: Methane trends 1990-2004 Global Mean Surface Methane (ppb) 1790 1780 1770 1760 Available emissions estimates for the past decade are fairly consistent with CH4 observations OBS ANTH+BIO BASE ANTH Dt decreases by 1.6% in BASE 1750 from 1991-1995 to 2000-2004 due to higher temp. (+0.3K) and OH (+1.2%); OH rise from enhanced lightning NOx 1740 1730 1720 1710 1990 1995 2000 2005 NEXT: Climate and air quality benefits from CH4 controls 1) Magnitude, spatial variability, linearity 2) Comparison with traditional O3 control strategies 3) Future scenarios Characterizing the methane-ozone relationship with idealized model simulations Reduce global anthropogenic CH emissions by 30% Surface Methane Tropospheric O34burden 0 0 -50 D Surface Methane Abundance (ppb) -2 -100 -4 -150 -200 -6 -250 -8 -300 DTropospheric O3 Burden (Tg) -10 -350 -400 -12 1 6 11 16 21 26 31 Simulation Year Model approaches a new steady-state after 30 years of simulation Is the O3 response sensitive to the location of CH4 emission controls? Change in July 2000 trop. O3 columns (to 200 hPa) 30% decrease in global anthrop. CH4 emissions -34 -27 -20 No Asia – (30% global decrease) Zero CH4 emissions from Asia (= 30% decrease in global anthrop.) -14 Dobson Units -7 mW m-2 (Radiative Forcing) Tropospheric O3 column response is independent of CH4 emission location except for small (~10%) local changes Target cheapest controls worldwide -5.1 -3.4 -1.7 DU -0.7 +0.7 mW m-2 Decrease in summertime U.S. surface ozone from 30% reductions in anthrop. CH4 emissions MAXIMUM DIFFERENCE (Composite max daily afternoon mean ozone JJA) NO ASIAN ANTH. CH4 Largest decreases in NOx-saturated regions Tropospheric O3 responds approximately linearly to anthropogenic CH4 emission changes across models MOZART-2 [West et al., PNAS 2006; this work] TM3 [Dentener et al., ACP, 2005] GISS [Shindell et al., GRL, 2005] X GEOS-CHEM [Fiore et al., GRL, 2002] IPCC TAR [Prather et al., 2001] Anthropogenic CH4 contributes ~50 Tg (~15%) to tropospheric O3 burden ~5 ppbv to surface O3 How much methane can be reduced? Ozone reduction (ppb) Cost-saving reductions 0.7 North America Rest of Annex I Rest of World (industrialized nations) 1.4 <$10 / ton CO2 eq. All identified reductions 00 1.9 10% of anth. emissions 20% of anth. emissions 20 40 60 80 100 120 20 40 60 80 100 -1 120 Methane Methane reduction reductionpotential potential(Mton (MtonCH CH4 4yryr)-1) IEA [2003] for 5 industrial sectors Comparison: Clean Air Interstate Rule (proposed NOx control) reduces 0.86 ppb over the eastern US, at $0.88 billion yr-1 West & Fiore, ES&T, 2005 Impacts of O3 precursor reductions on global surface O3 Steady-state change in 8-hr daily maximum surface O3 averaged over 3-month “O3 season” from 20% reductions in global anthropogenic emissions NOx NMVOC ppbv CO CH4 MOZART-2 model (2.8° x 2.8°) ppbv West et al., submitted Double dividend of methane controls: Improved air quality and reduced greenhouse warming AIR QUALITY: Change in population-weighted mean 8-hr daily max surface O3 in 3-month “O3 season” (ppbv) CLIMATE: Radiative Forcing (W m-2) NOx OH CH4 20% 20% 20% 20% 20% 20% 20% 20% anth. anth. anth. anth. anth. anth. anth. anth. NMVOC CO NOx NMVOC CO CH4 NOx CH4 Steady-state results from MOZART-2 West et al.,submitted Will methane emissions increase in the future? Anthropogenic CH4 emissions (Tg yr-1) Dentener et al., ACP, 2005 A2 B2 MFR Current Legislation (CLE) Scenario PHOTOCOMP for IPCC AR-4 used CLE, MFR, A2 scenarios for all O3 precursors [Dentener et al., 2006ab; Stevenson et al., 2006; van Noije et al., 2006; Shindell et al., 2006] Our approach: use CLE as a baseline scenario & apply methane controls Policy-relevant methane control scenarios to 2030 Anthropogenic CH4 emissions (Tg yr-1) 500 +29% from 2005 to 2030 under CLE 450 400 CH4 (Tg 350 2030 decrease relative to CLE: 300 250 200 150 100 50 0 2000 CLE A: -75 Tg (18% of 2030 anthrop. CH4 emis.) Scen A B: -125 Tg (29%) Scen B Scen C c/o J.J. West 2005 2010 2015 2020 2025 C: -180 Tg (42%) 2030 Transient, full-chemistry simulations in MOZART-2; 2000-2004 NCEP meteorology, recycled for 2005-2030 Other O3 precursor emissions follow the 2005-2030 CLE baseline: Anthrop. NOx emissions increase by 5.3 Tg N (+19%) Anthrop. CO emissions decrease by 44 Tg CO (-10%) Preliminary results: Impacts on climate and global surface ozone Radiative Forcing (W m-2) 2005 to 2030 +0.16 Net Forcing 30.5 +0.08 0.00 -0.08 ppb 30 GlobalAnnual Annual Mean Surface Surface Ozone Global Mean O3 CLE A B CLE C 2030 29.5 29 28.5 28 2005 2010 2015 2020 Year CLE A B C Scenario C stabilizes despite 5 Tg N increase in anth. NOx Cost-benefit analysis in progress... 2025 2030 Regional control efforts (even under optimistic scenarios) may be offset by increases in hemispheric ozone pollution By 2030 under the CLE scenario, “the benefit of European emission control measures is… significantly counterbalanced by increasing global O3 levels…” [Szopa et al., GRL, 2006] U.S. air quality degrades despite domestic emissions controls (A1 2030) 1995 Base case 2030 A1 IPCC 2030 Scenario A1 Anthrop. NOx emis. Global U.S. +80% -20% Methane emis. +30% GEOS-Chem Model (4°x5°) [Fiore et al., GRL, 2002] longer O3 season International approach to ozone abatement? TF HTAP multi-model assessment of intercontinental source-receptor relationships www.htap.org Co-Chairs: Terry Keating (U.S. EPA), Andre Zuber (EC) Intercontinental Source-Receptor Regions http://aqm.jrc.it/HTAP Experiment Set 1 (~20 models): Decrease precursor emissions by 20% in source regions Estimate pollutant response over receptor regions Inform 2007 review of CLRTAP Gothenburg Protocol Methane trends: Connecting climate and O3 chemistry Methane (ppb) 1790 1780 1770 1760 OBS BASE ANTH ANTH+BIO 1750 1740 1730 1720 1710 1990 0.18 1995 2000 METHANE TRENDS FROM 1990 TO 2004 • Simulation with time-varying emissions and meteorology best captures observed CH4 distribution 2005 • Model trend driven by increasing T, OH DtOH 91-95 to 01-04 0.16 • Trends in global lightning activity? Potential for climate feedbacks (on sources and sinks) 0.14 0.12 0.1 0.08 0.06 + 0.04 0.02 0 DT = DOH climT climOH BASE Ozone reduction (ppb) BASE North America Rest of Annex I Rest of World Cost-saving reductions • Independent of reduction location Target cheapest controls worldwide <$10 / ton CO2 eq. All identified reductions 0 20 40 60 80 100 CLIMATE AND AIR QUALITY BENEFITS FROM CH4 CONTROL 120 • Reduces climate forcing and surface O3 Methane reduction potential (Mton CH 4 yr-1) Methane Surface Concentration Global mean surface CH4 2100 • Rising hemispheric background O3 may offset domestic efforts to reduce pollution Opportunity for international air quality management 2000 ppb 1900 1800 1700 1600 1500 2005 • Complementary to NOx, NMVOC controls 2010 2015 2020 Year 2025 2030