Background Ozone in Surface Air: Origin, Variability, and Policy Implications Arlene M. Fiore Goddard Institute for Space Studies May 20, 2005.

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Presentation transcript:

Background Ozone in Surface Air: Origin, Variability, and Policy Implications Arlene M. Fiore Goddard Institute for Space Studies May 20, 2005

Acknowledgments Daniel Jacob Mat Evans Duncan Fairlie Brendan Field David Streets Suneeta Fernandes Carey Jang Qinbin Li Hongyu Liu Bob Yantosca Jason West Denise Mauzerall Larry Horowitz Chip Levy

NO x VOC NO x VOC CONTINENT 2 OCEAN O3O3 Boundary layer (0-3 km) Free Troposphere CONTINENT 1 What is the origin of tropospheric ozone? OH HO 2 VOC, CH 4, CO NO NO 2 h O3O3 O3O3 Hemispheric Pollution Direct Intercontinental Transport air pollution (smog) Stratospheric O 3 Stratosphere ~12 km

Number of People Living in U.S. Counties Violating National Ambient Air Quality Standards (NAAQS) in 2001 EPA [2002] 124 ppbv: ppbv: Carbon monoxide (CO) Lead Nitrogen dioxide Ozone (O 3 ) Particles < 10  m (PM 10 ) Particles < 2.5  m (PM 2.5 ) Sulfur dioxide (SO 2 ) Any pollutant Millions of People

The Risk Increment Above the Background is Considered when setting the NAAQS for Ozone Environmenta l risk Ozone Concentration Policy-Relevant Background NAAQS Acceptable added risk  Need a quantitative estimate for background ozone  EPA chose a constant value (40 ppbv) in previous review of O 3 standard

Range of “background O 3 ” estimates in U.S. surface air O 3 (ppbv) Range considered by EPA during last revision of O 3 standard 84 ppbv: threshold for current U.S. O 3 standard Frequent observations previously attributed to natural background [Lefohn et al., 2001] Range from prior global modeling studies Range from this work [Fiore et al., 2003] The U.S. EPA considers background levels when setting the NAAQS Used by EPA to assess health risk from O 3 (1996)

FiresLand biosphere Human activity Ocean NORTH AMERICA NORTH AMERICA Lightning “Background” air X Outside natural influences Long-range transport of pollution “POLICY RELEVANT BACKGROUND” OZONE : Ozone concentrations that would exist in the absence of anthropogenic emissions from North America [EPA CD, 2005] stratosphere lightning Policy Relevant Background is not directly observable  Must be estimated with models

GEOS-CHEM [Bey et al., 2001] MOZART-2 [Horowitz et al., 2003] Approach: Insights from two chemical transport models GEOS-3 GMAO met 2°x2.5°; 30  -levels Synoz upper boundary NCEP meteorology T62 (1.9°) ; 28  -levels Strat O 3 relaxed to climatology PRODLOSSDEPSTRAT Ozone (Tg yr -1 ) X 19-Model Mean MOZART GEOS-CHEM Ozone Budgets in IPCC-AR4 Tropospheric Chemistry Models AR4 budgets c/o Jérôme Drevet David Stevenson Frank Dentener

X Elevated sites (> 1.5 km) Low-lying sites 1. quantify PRB O 3 and its various sources 2. diagnose origin of springtime high-O 3 events at remote U.S. sites, previously attributed to natural, stratospheric influence Approach: 2001 CASTNet Observations (EPA, NPS)

Case Study #1: Voyageurs National Park, Minnesota (May-June 2001) CASTNet observations Model Background Natural O 3 level Stratospheric + * Hemispheric pollution Regional pollution }  } PRB: ppbv Natural level: 9-23 ppbv Stratosphere: < 7 ppbv High-O 3 events: dominated by regional pollution; minor stratospheric influence (~2 ppbv) regional pollution hemispheric pollution X Lefohn et al. [2001] suggest a stratospheric source as the likely origin of high-O 3 events frequently observed in June Model Results from GEOS-CHEM

CASTNet observations Model PRB Natural O 3 level Stratospheric + * Hemispheric pollution Regional pollution }  } Background at high-altitude site (2.5 km) not necessarily representative of background contribution at low-lying sites X regional pollution hemispheric pollution Frequent high-O 3 events previously attributed to natural, stratospheric source [Lefohn et al., 2001] Case Study #2: Yellowstone National Park, Wyoming (March-May 2001) Model Results from GEOS-CHEM

Both models show that PRB ozone is higher at high-altitude site 19 May – June 2001 * CASTNet observations Mar – May 2001 GEOS-CHEM Model GEOS-CHEM PRB MOZART Model MOZART PRB 15-36; ; ; ; 35 PRB Range; mean Elevation: 430 m Elevation: 2470 m

PRB ozone is lower under polluted conditions: typically below 25 ppbv Regional Pollution Ozone (ppbv) Cumulative Probability Daily mean afternoon O 3 at 58 low-elevation U.S. CASTNet sites June-July-August CASTNet sites GEOS-CHEM Model PRB Ozone *  Assuming constant 40 ppbv background underestimates health risks on most polluted days

Compiling daily afternoon (1-5 p.m. mean) surface ozone from all CASTNet sites for March-October 2001: PRB ozone is typically ppbv Probability ppbv -1 CASTNet sites GEOS-CHEM Model at CASTNet Natural 18±5 ppbv GEOS-CHEM PRB 26±7 ppbv GEOS-CHEM PRB 29±9 ppbv MOZART-2  Hemispheric Pollution enhances U.S. PRB by 8±4 ppbv  Prior work suggests 6 ppbv from anthrop. CH 4 on average

Radiative Forcing of Climate from Preindustrial to Present: Important Contributions from Methane and Ozone Hansen, Scientific American, 2004

50% anth. NO x 50% anth. CH 4 50% anth. VOC 1995 (base) 50% anth. VOC 50% anth. CH 4 50% anth. NO x AIR QUALITY: Number of U.S. summer grid-square days with O 3 > 80 ppbv CLIMATE: Radiative Forcing (W m -2 ) Fiore et al., GRL, 2002 Double dividend of Methane Controls: Decreased greenhouse warming and improved air quality Decreased greenhouse warming and improved air quality  Methane links air quality and climate via background ozone

Response of Global Surface Ozone to 50% decrease in global methane emissions (actually changing uniform concentration from 1700 to 1000 ppbv) Ozone decreases by 1-6 ppb ~3 ppb over land in US summer ** ~60% of reduction in 10 yr; ~80% in 20 yr.

How Much Methane Can Be Reduced? Top bar: IEA (2003), for 5 industrial sectors. Lower bar: EPA (2003), for 4 industrial and 1 agricultural sector. Comparison: Clean Air Interstate Rule (proposed) reduces 0.86 ppb over the eastern US, at $0.88 billion yr -1, through NO X control. West & Fiore, ES&T, 2005

Tropospheric ozone response to anthropogenic methane emission changes is fairly linear Shindell et al., 2005 report that tropospheric ozone responds linearly to 10, 25, 50, 75, 100% decreases in anthropogenic CH 4 X MOZART-2 (this work) TM3 [Dentener et al., ACPD, 2005] GISS [Shindell et al., GRL, 2005 GEOS-CHEM [Fiore et al., GRL, 2002] IPCC TAR [Prather et al., 2001]

Methane Emissions in EDGAR inventory early 1990s; Tg CH 4 yr -1 Energy, landfills, wastewater95 Ruminants93 Rice60 Biomass burning86 Ocean10 Biogenic204 TOTAL547 Cut Global Anthropogenic by 40%: (1) All in Asia (2) Everywhere in the globe  Are ozone decreases independent of CH 4 source location? Anthropogenic Natural

Zero anthrop. CH 4 emissions from Asia Global 40% decrease in anthrop. CH 4 emis. Zero Asia – global 40% July 2000 surface O 3 change mainly independent of CH 4 source location, slightly larger response in source region (Transient simulations with EDGAR 1990 emissions, beginning 1990) OZONE METHANE

U.S. Surface Afternoon Ozone Response in Summer also independent of methane emission location MEAN DIFFERENCE MAX DIFFERENCE (Max daily mean afternoon JJA) NO ASIAN CH 4 GLOBAL 40% DECREASE IN ANTHROP. CH 4  Stronger Sensitivity in NO x -saturated regions (Los Angeles)

Local CH 4 oxidation contributes up to ~30% of the total decrease in surface O 3 from lowering CH 4 concentrations in a NO x -saturated region Change in MOZART-2 surface afternoon (1-5 p.m.) O 3 concentration after 1 day, when a 300 ppbv decrease in CH 4 concentrations is imposed below 800 hPa in Los Angeles /23/00 ppbv O 3

CLIMATE IMPACTS: Change in July 2000 Trop. O 3 Columns (to 200 hPa) 40% decrease in global anthrop. CH 4 emissions Zero CH 4 emissions from Asia (= 40% decrease in global anthrop.) No Asia – (40% global decrease) Tropospheric O 3 column response is independent of CH 4 emission location except for small (~10%) local changes Dobson Units DU

Assume 25 ppb threshold, CH 4 reductions starting in 2000 AIR POLLUTION IMPACTS: 2030 Avoided Premature Mortalities (A2 scenario - 65 Tg CH 4 emissions) West et al., 2005 Change in 8-hr summer surface ozone from a 20% decrease in global anthrop. methane emissions Avoided Mortalities in 2030 Reducing anthrop. CH 4 emis. by 20% (starting in 2000): -- decreases global surface ozone (~1 ppbv in populated areas) -- prevents ~34,000 premature deaths in 2030

Should these be science conclusions from paper incorporated into Criteria document And/or a summary of the talk focused on model evaluation? 1. Policy-Relevant Background in surface air over the United States: -- 25±5 ppbv at low-elevation sites in summer -- varies with season, altitude; anti-correlated with high domestic O ±4 ppbv from hemispheric pollution (~5-7 ppbv from anthr. CH 4 )  40 ppbv previously used by EPA underestimates health risks  international negotiations to reduce hemispheric background would facilitate compliance with more stringent standardsConclusions 2. 20% reductions in anthrop. methane emissions possible now: -- reduce surface ozone globally by ~1 ppbv in populated regions -- lower global radiative forcing by ~0.13 W m avoid 34,000 premature mortalities in Climate and air quality benefits from controls on anthropogenic methane emissions are largely independent of source location -- small enhancements (~10%) in source region -- enhanced surface ozone response (up to ~30% total response) to CH 4 changes in NO x -saturated regions