1 1 First Stage of Upper-stratospheric Ozone Recovery Mike Newchurch/UAH Eun-Su Yang/Georgia Tech...

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1 1 First Stage of Upper- stratospheric Ozone Recovery Mike Newchurch/UAH Eun-Su Yang/Georgia Tech Derek Cunnold/Georgia Tech Greg Reinsel/U Wisconsin, Madison Joe Zawodny/LaRC Jim Russell/Hampton U Presented at AGU Fall Meeting San Francisco, CA 12 December, 2003

Transcript of 1 1 First Stage of Upper-stratospheric Ozone Recovery Mike Newchurch/UAH Eun-Su Yang/Georgia Tech...

Page 1: 1 1 First Stage of Upper-stratospheric Ozone Recovery Mike Newchurch/UAH Eun-Su Yang/Georgia Tech Derek Cunnold/Georgia Tech Greg Reinsel/U Wisconsin,

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First Stage of Upper-stratospheric

Ozone Recovery

Mike Newchurch/UAHEun-Su Yang/Georgia Tech

Derek Cunnold/Georgia TechGreg Reinsel/U Wisconsin, Madison

Joe Zawodny/LaRCJim Russell/Hampton U

Presented at

AGU Fall MeetingSan Francisco, CA

12 December, 2003

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In the upper stratosphere, it’s the chlorine25 yrs Stratospheric ballooning (Europe, Canada, USA)+ Space Lab-3 ATMOS (1985)

+ ATLAS 1, 2, 3 (1992,3,4: ATMOS, MAS, SSBUV, SUSIM)

+ 30 yrs laboratory kinetics measurements

+ 30 yrs photochemical modeling

+ NASA, ESA, Japanese, Canada satellites (BUV, SBUV, SAGE I/II, TOMS, UARS, ADEOS, GOME, ACE, ENVISAT)

+ 50 yrs Ground-based RS: Dobson/Umkehr, many others

+ 20 yrs Ground-based in situ CFC & HCFC obs

+ Lower Stratospheric aircraft obs (ER2 campaigns)

+ 1000s of scientists thoughts and analyses

→ A very good understanding of Upper stratospheric chemistry: The Protocol is working on Chlorine

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Fahey et al., 20 questions, 2003http://www.unep.org/ozone/faq.shtml

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Chlorine turning over @ sfc, slowing down @ 40 km

Fahey et al., 20 questions, 2003http://www.unep.org/ozone/faq.shtmlSee also Montzka, Cunnold, Remsberg

Newchurch et al., 2003

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What do we expect in ozone?

WMO Ozone Assessment, 2003, fig 4-43

5 Stages of Recovery

1: Slowdown in loss rate2: Minimum3: Increasing ozone4: Slowdown in increase5: Full recovery

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Alt

itud

e (k

m)

30

50

40

0 2 4 6–2

Percent Change in Ozonecirca 2010 (relative to 2000)

Cly

Cly

H2O

Cly CH4

Cly T

Sensitivity of Future Changes in Ozone to Cly, H2O, and CH4.

All forcings are based onan extrapolation of presenttrends. This extrapolationis perhaps most uncertainfor H2O and CH4.

Jucks and Salawitch, AGU Monographs, 2000

Model Forcings

Cly 15% H2O 1.0 ppm CH4 0.1 ppm

T ~2 K

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The ozone trend model

[O3]t = + t + [Seasonal terms] + [QBO periodic terms] + γ [F10.7]t + Nt

is the mean level,

is a linear trend coefficient,

the seasonal terms represent the 12-, 6-, 4-, and/or 3-months cosine terms each with a time lag

See poster A41D-0718 by Yang et al. AGU Fall Meeting, 2003

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The ozone trend model

[O3]t = + t + [Seasonal terms] + [QBO periodic terms] + γ [F10.7]t + Nt

is the mean level,

is a linear trend coefficient,

the seasonal terms represent the 12-, 6-, 4-, and/or 3-months cosine terms each with a time lag

The Quasi Biennial Oscillation periodic terms consist of cosines with time lags to represent QBO signal with periods between 3 and 30 months excluding 12-, 6-, 4-,and/or 3-months terms. The traditional approach of using Singapore winds with a fitted lag produces similar results, but with less precise trend estimates and more fluctuations in the residuals.

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The ozone trend model

[O3]t = + t + [Seasonal terms] + [QBO periodic terms] + γ [F10.7]t + Nt

is the mean level,

is a linear trend coefficient,

the seasonal terms represent the 12-, 6-, 4-, and/or 3-months cosine terms each with a time lag

The QBO periodic terms consist of cosines with time lags to represent QBO signal with periods between 3 and 30 months excluding 12-, 6-, 4-,and/or 3-months terms. The traditional approach of using Singapore winds with a fitted lag produces similar results, but with less precise trend estimates and more fluctuations in the residuals.

[F10.7]t is the F10.7-cm radio flux density which is used to provide a solar variation proxy.

γ is a solar signal regression coefficient.

Nt is the autocorrelated error term, for which a first order autoregressive process is assumed (Nt = a1Nt-1 + t).

The t residuals, after removing the autoregressive component, a1Nt-1, are the residuals that are used to compute the cumulative sums of residuals described in Appendix B.

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The ozone trend model

[O3]t = + t + [Seasonal terms] + [QBO periodic terms] + γ [F10.7]t + Nt

The ability to determine trend changes early with high confidence depends on:

Data quality (ozone and proxies)

Density of data coverage

Quality of the model fitting

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1111

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Upper Stratosphere

Lower Stratosphere

Southern latitudes Tropics Northern latitudes

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Northern MidlatitudeUpper Stratosphere

TropicsUpper Stratosphere

Southern MidlatitudeUpper Stratosphere

SAGE observations

HALOE observations 2-σ confidence envelope

Measurements above projected trend

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Presented at the National Press ClubWashington, D.C. July 29, 2003

>100 news storiesLive TV, radio interviews

All time high hit AGU, #1 2003 AAAS EurekAlert 40k hits (2x #2 story)

Top 100 Discover story

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

2. The ozone amount is still DECREASING, but more slowly than before 1997.

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

2. The ozone amount is still DECREASING, but more slowly than before 1997.

3. The chlorine amounts (from CFC releases at the surface) are decreasing at Earth’s surface and increasing more slowly in the upper stratosphere as a result of the Montreal Protocol and its amendments.

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

2. The ozone amount is still DECREASING, but more slowly than before 1997.

3. The chlorine amounts (from CFC releases at the surface) are decreasing at Earth’s surface and increasing more slowly in the upper stratosphere as a result of the Montreal Protocol and its amendments.

4. Because Chlorine chemistry controls a significant amount of the ozone loss in the upper stratosphere, the Protocol is having the DESIRED EFFECT on the ozone layer, but full recovery is still decades away.

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

2. The ozone amount is still DECREASING, but more slowly than before 1997.

3. The chlorine amounts (from CFC releases at the surface) are decreasing at Earth’s surface and increasing more slowly in the upper stratosphere as a result of the Montreal Protocol and its amendments.

4. Because Chlorine chemistry controls a significant amount of the ozone loss in the upper stratosphere, the Protocol is having the DESIRED EFFECT on the ozone layer, but full recovery is still decades away.

5. Access to highly calibrated, long-term satellite measurements and international ground-based measurements was essential to detecting these small but important changes.

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Conclusions1. Ozone measurements by satellites and international ground stations show

compelling evidence of the BEGINNING of the recovery of the ozone in the UPPER stratosphere.

2. The ozone amount is still DECREASING, but more slowly than before 1997.

3. The chlorine amounts (from CFC releases at the surface) are decreasing at Earth’s surface and increasing more slowly in the upper stratosphere as a result of the Montreal Protocol and its amendments.

4. Because Chlorine chemistry controls a significant amount of the ozone loss in the upper stratosphere, the Protocol is having the DESIRED EFFECT on the ozone layer, but full recovery is still decades away.

5. Access to highly calibrated, long-term satellite measurements and international ground-based measurements was essential to detecting these small but important changes.

6. We are not out of the woods yet. We have been surprised before by atmospheric changes and must continue to carefully measure our atmosphere to avoid being surprised again, perhaps by climate-change interactions.

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Future ?1. Is ozone recovering in the lower stratosphere?

2. What are the effects of global climate change on ozone recovery?

3. What observational capacity is necessary to adequately answer #1 and #2?1. Measure ozone evolution2. Measure climate changes

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http://nsstc.uah.edu/atmchem/

Support from NASAEarth Science Enterprise