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Supplementary materials for : Characteristics of

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tropospheric ozone depletion events in the Arctic

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spring: Analysis of the ARCTAS, ARCPAC,

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and ARCIONS measurements

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J.-H. Koo, Y. Wang, T. P. Kurosu, K. Chance,

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A. Rozanov, A. Richter, S. J. Oltmans, A. M. Thompson,

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J. W. Hair, M. A. Fenn, A. J. Weinheimer, T. B. Ryerson,

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S. Solberg, L. G. Huey, J. Liao, J. E. Dibb, J. A. Newman,

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J. B. Nowak, R. B. Pierce, M. Natarajan, and J. Al-saadi

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Fig. S1. Vertical profiles of correlation coefficients (R values) of retrieved tropospheric 26

BrO columns with BrO measured from DC-8 Flights 9 and 10 (April 16 and 17). To 27

correlate with tropospheric BrO columns with sufficient in situ data points, we integrate in 28

situ aircraft observations of BrO, Br2+HOBr, and soluble bromide from the surface to 7 29

altitude levels (100, 300, 500, 750, 1000, 1500, and 2000 m). Tropospheric column BrO 30

measurements corresponding to the in situ data points were sampled along the flight tracks.

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WP-3D data were not used because no significant correlation was found with column BrO;

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the reason is unclear. We used six tropospheric BrO VCD products, which are OMI-20th 33

(black), OMI-SCIA2ND (red), OMI-RAQMS (green), GOME2-20th (yellow), GOME2- 34

SCIA2ND (blue), and GOME2-RAQMS (purple).

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Fig. S2. Same as Fig. S1, but for correlations with integrated Br2+HOBr in DC-8 flights 44

(April 4, 5, 8, 9, 12, 16, and 17).

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Fig. S3. Same as Fig. S2, but for correlations with integrated soluble bromide measured in 62

DC-8 flights.

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Fig. S4. Same as Fig. S1, but for correlations with integrated Br2+HOBr in WP-3D flights 78

(on April 12, 15, 18, 19, and 21). The more consistent correlation with Br2+HOBr 79

measurements during ARCPAC than ARCTAS (Fig. S2) reflects in part a smaller 80

sampling region by WP-3D (to be shown in Fig. 5). The smaller sampling region leads to 81

a smaller variation of the estimated stratospheric column BrO during ARCPAC than 82

ARCTAS. The variation of tropospheric column BrO is therefore more consistent among 83

the different products during ARCPAC than ARCTAS.

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Fig. S5. Same as Fig. 2a, but for tropospheric BrO VCDs of OMI-SCIA2ND.

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Fig. S6. Same as Fig. 2a, but for tropospheric BrO VCDs of GOME2-20th. 106

107 108 109

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Fig. S7. Same as Fig. 2a, but for tropospheric BrO VCDs of OMI-20th. 116

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Fig. S8. Same as Fig. 2a, but for tropospheric BrO VCDs of GOME2-RAQMS.

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Fig. S9. Same as Fig. 2a, but for tropospheric BrO VCDs of OMI-RAQMS.

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Fig. S10. Same as Fig. 5, for tropospheric BrO VCDs of OMI-SCIA2ND.

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Fig. S11. Same as Fig. 5, but for tropospheric BrO VCDs of GOME2-20th. 155

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Fig. S12. Same as Fig. 5, but for tropospheric BrO VCDs of OMI-20th. 164

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Fig. S13. Same as Fig. 5, but for tropospheric BrO VCDs of GOME2-RAQMS.

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Fig. S14. Same as Fig. 5, but for tropospheric BrO VCDs of OMI-RAQMS.

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Fig. S15. Hourly surface ozone as a function of temperature at Barrow for February (left) 191

and March (right). Ozone measurements from 1979 to 2008 were obtained from the 192

NOAA Earth System Research Laboratory (ESRL) and the temperature dataset from the 193

NOAA National Climate Data Center (NCDC).

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Fig. S16. Same as Fig. 9, but for tropospheric BrO VCDs of OMI-SCIA2ND.

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Fig. S18. Same as Fig. 9, but for tropospheric BrO VCDs of OMI-20th. 224

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Fig. S20. Same as Fig. 9, but for tropospheric BrO VCDs of OMI-RAQMS.

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