Articles | Volume 19, issue 4
https://doi.org/10.5194/amt-19-1465-2026
© Author(s) 2026. This work is distributed under the Creative Commons Attribution 4.0 License.
Balloon-borne stratospheric vertical profiling of carbonyl sulfide and evaluation of ozone scrubbing materials
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- Final revised paper (published on 26 Feb 2026)
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RC1: 'Comment on egusphere-2025-3079', Anonymous Referee #1, 12 Aug 2025
- AC1: 'Reply on RC1', Alessandro Zanchetta, 03 Oct 2025
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RC2: 'Comment on egusphere-2025-3079', Anonymous Referee #2, 25 Aug 2025
- AC2: 'Reply on RC2', Alessandro Zanchetta, 03 Oct 2025
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AR by Alessandro Zanchetta on behalf of the Authors (03 Oct 2025)
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ED: Referee Nomination & Report Request started (27 Oct 2025) by Nicholas Deutscher
RR by Anonymous Referee #1 (31 Oct 2025)
ED: Publish subject to minor revisions (review by editor) (15 Jan 2026) by Nicholas Deutscher
AR by Alessandro Zanchetta on behalf of the Authors (23 Jan 2026)
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ED: Publish subject to minor revisions (review by editor) (04 Feb 2026) by Nicholas Deutscher
AR by Alessandro Zanchetta on behalf of the Authors (05 Feb 2026)
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ED: Publish as is (20 Feb 2026) by Nicholas Deutscher
AR by Alessandro Zanchetta on behalf of the Authors (20 Feb 2026)
Manuscript
Summary
This manuscript evaluates strategies to mitigate ozone (O₃) contamination during stratospheric sampling of carbonyl sulfide (OCS) using the AirCore balloon system. The primary finding is that O₃ does not appear to significantly affect OCS measurements across the atmospheric column: AirCore profiles with and without O₃ scrubbing agree well with independent datasets from ACE-FTS and SPIRALE. Observed differences from these datasets fall within the QCLS measurement precision and the expected natural variability, particularly in high-latitude regions where seasonal OCS changes can reach ~150 ppt (https://gml.noaa.gov/hats/gases/OCS.html).
The authors tested three inlet O₃ filtration strategies: cotton, magnesium perchlorate [Mg(ClO₄)₂], and squalene. Laboratory results show that cotton is ineffective at removing O₃ (Figure S2), and squalene was not deployed during balloon flights. Thus, only Mg(ClO₄)₂-filtered and unfiltered (“free inlet”) profiles provide field-relevant comparisons. However, because the Mg(ClO₄)₂ dryer was not characterized in laboratory experiments, its O₃ removal efficiency in the field remains uncertain.
The motivation for O₃ mitigation stems from Engel et al. (1994), which reported up to 50% OCS loss when co-sampled with stratospheric O₃ in balloon-borne cryogenic samplers. Notably, in the nearly three decades since, no widely cited studies have confirmed such losses, suggesting that the effect may be specific to cryogenic sampling techniques. If so, the null result reported in this manuscript has important implications for interpreting historical in-situ stratospheric trace gas records.
Major Comments
The laboratory results presented in this manuscript appear to contradict the findings of Engel et al. (1994). Specifically, Figure A2 shows a slight enhancement in OCS (~40 ppt) in the presence of stratospheric O₃ concentrations, whereas Engel reported up to a 50% loss of OCS under similar O₃ levels. Given the significance of these laboratory results to the paper’s conclusions, I recommend moving most of the information currently in Appendix A into the main body of the manuscript. However, it should be noted that the enhancement reported here is less than 10% of typical ambient OCS levels and approaches the instrument’s stated precision (~25 ppt), making it unclear whether the observed difference is statistically meaningful.
Due to the substantial natural variability in tropospheric OCS abundance and in stratospheric OCS driven by transport processes, I do not consider it appropriate to perform a quantitative comparison of short-duration datasets separated by several years. I therefore recommend removing Figures 2, 6, and 7 as well as Tables 3 and 5. Table 2 could be moved to the Supplementary Information or omitted entirely, as its contents are already conveyed in Figure 1. Alternatively, a comparison with N₂O or other stratospherically photolytic tracers such as CFCs could allow for quantification of stratospheric transport, but this would require substantial additional analysis and constitute a major revision to the manuscript.
The manuscript includes significant caveats regarding the LISA and BIG LISA MLF “bag” sampler data. In Section 4.1.2, the authors note that the 30229-U MLF bags used in BIG LISA have a manufacturer warning: “Although the deployed bags are indicated as suitable for sulfur compounds, they are not recommended for low-ppm volatile organic compounds due to background levels” (Sigma Aldrich, 2025). A similar warning appears on the Sigma Aldrich website for the 30228-U bags used in LISA: “Not recommended for low ppm VOCs due to background levels (we recommend the SupelInert PVDF Tedlar alternative film for VOCs)”. Considering that a common VOC such as CS₂ can oxidize to OCS with ~80% efficiency, even sub-ppm VOC contamination could significantly bias atmospheric OCS measurements (<1 ppb). In addition, a subset of the LISA OCS data appears to have been omitted by the authors without explanation (see Section 2.1.2). Given these concerns, I recommend removing the LISA dataset analysis from the manuscript.
Specific Comments:
Line 48: Remove: “Although the debate has not been fully resolved”
Line 59: Provide a reference for the QCLS
Line 66: Please explain why the impact of air samples of COS may be significant. I can find no other examples aside from the Engel 1994 paper.
Line 72: Add a reference to the Schmidt et al 2024:
Schmidt, Matthew, et al. "Trends in atmospheric composition between 2004–2023 using version 5 ACE-FTS data." Journal of Quantitative Spectroscopy and Radiative Transfer 325 (2024): 109088.
Line 83: Explain how Aircore and Sulfinert specifically differs from the stratospheric Cryogenic air sampler apparatus.
Line 102: Do you expect any Aqueous reactions with ozone to occur on the wetted cotton?
Line 146: What is the duration of the samples storage in: 1. MLF bags, 2. glass cylinders before analysis
Lines 149-151: Without a specific reason to disregard a subset of samples, you must either present all of the data or none of it.
Lines 205-207: Please present the data for the QCLS precision.
Lines 211-212: Present the data or references for the QCLS precision.
Line 215: Which version of ACE-FTS are you using v5.2? v5.3?
Line 216: Add Boone et al 2023. And Schmidt et al 2024:
Boone, C. D., P. F. Bernath, and M. Lecours. "Version 5 retrievals for ACE-FTS and ACE-imagers." Journal of Quantitative Spectroscopy and Radiative Transfer 310 (2023): 108749.
Line 228: Do the 502 and 1681 profiles correspond to global samples at those latitude bands or localized profiles over TRN and KRN?
Line 244: This analysis would be more quantitative if you compared with the Age of Air parameter or another photolytic species like N2O.
Line 263: The MkIV spectrometer utilized by Toon et al is balloon borne into the stratosphere, but this is a long path solar FTIR measurements so it may be more appropriate to include with the remote sensing measurements.
Line 278: Please provide more details for the “direct reaction of other gas species with O2.”
Line 284: How does your observed tropospheric variability compare with NOAA GML flask network measurements for high latitudes?
Line 290: How is the variable lapse rate an indicator of OCS convective transport? Have you preformed trajectory analysis?
Line 299-301: The low-ppm VOC warning is listed for both LISA and Big-LISA MLF bags.
Line 317: The absolute differences in OCS above the tropopause are not useful. You must compare with N2O to understand stratospheric transport and age of air factors, and correct for N2O increasing trend.
Line 323: Include Schmidt et al 2024 to for stratospheric OCS trends.
Line 331: On line 327 the authors state that no quantification of sample loss is available, but here they claim that “differences remain marginal.” Please attempt to provide more quantification of the uncertainties
Line 339: The changing relationship between Methane and N2O is interesting and either points to major instrument issues or more complex stratospheric dynamics and should be discussed more here.
Line 370: The temporal differences really limit any kind of quantitative analysis.
Line 383: How does the 8% difference compare with the decadal change in stratospheric OCS abundance?
Line 400: This qualitative comparison is not useful, just refer to Figure 3
Line 413: What version of ACE-FTS are you using?
Line 476: Add discussion of Squalene-based scrubbers to the main body of the text.
Line 479: This is a major result, and you should highlight the difference from Engel’s 1994 paper.