Any statement of the form "artificial stratospheric sulfate injection would
induce significant X" is obviously wrong, given that at a minimum any
effect depends on how much you do.  And we need an assessment of the
overall trade-offs, not mindless throwing out of options based on any one
single effect.

In the case of ozone, there's lots of papers on this, and there will be
more; the answer of course depends on how much you do, on what latitudes
you inject at, on when you start, but there's also a lot more to it than
just the heterogeneous chemistry response; when you include all of the
dynamical and chemical responses then in some places total column ozone
goes up (over Antarctic it consistently goes down - though if you start in
2035 to maintain temperatures at 2030 levels, then in CESM(WACCM)
simulations, Antarctic ozone levels might drop to levels not seen since
2025... is that a reason to ignore SAI?)


On Fri, Oct 17, 2025 at 12:45 PM Oeste <[email protected]> wrote:

> Hi Clive and Oswald,
>
> The authors of the paper below state, that enhanced stratospheric sulfate
> aerosol levels from volcanic eruptions or artificial stratospheric sulfate
> injection would induce *significant* stratospheric ozone depletion.
>
> Volcanic sulfate injections are only during the volcanic maximum eruption
> period active. These eruption periods last very seldom more than a month.
> Stratospheric Aerosol Injection (SAI) periods are longer than 100 years.
> Hence the skin cancer inducing UV-C radiation problem induced by
> the stratospheric ozone depletion will also last for more than 100 years.
>
> Because we know some much more economic and efficient climate restoration
> methods this should make no problems for climate restoration.
>
> Franz
>
>
> Am 17.10.2025 um 13:32 schrieb Geoengineering News:
>
> https://agupubs.onlinelibrary.wiley.com/doi/10.1029/2025JD043786?af=R
>
> *Authors: *Laila V. Howar, Ross J. Salawitch, David M. Wilmouth, Eric J.
> Hintsa, Jennifer S. Hare, Thomas F. Hanisco, Jason M. St. Clair, Erin R.
> Delaria, Elliot L. Atlas, Sue Schauffler, Kate R. Smith, Jessica B. Smith,
> Bradley D. Hall, Fred L. Moore, Jasna V. Pittman, Bruce Daube, T. Paul Bui,
> Yaowei Li, Frank N. Keutsch, David S. Sayres, Steven C. Wofsy, Jonathan
> Dean-Day, Stephen Donnelly, Victoria A. Treadaway, James G. Anderson,
> Cameron R. Homeyer, Kenneth P. Bowman
>
> *14 October 2025*
>
> https://doi.org/10.1029/2025JD043786
>
> *Abstract*
> Studies have suggested that ClO could be enhanced within convectively
> influenced air masses in the North American Monsoon Anticyclone due to low
> temperature and elevated water mixing ratio conditions that are conducive
> to chlorine activation, potentially leading to significant loss of ozone in
> the midlatitude lowermost stratosphere. We analyze in situ measurements of
> temperature, pressure, ClO, ClONO2, H2O, NO2, aerosol surface area density
> (SAD), and organic chlorine species obtained by instruments aboard the NASA
> ER-2 over the continental US during the Dynamics and Chemistry of the
> Summer Stratosphere (DCOTSS) campaign to show that chlorine activation
> large enough to affect loss of ozone was not observed, for the summers of
> 2021 and 2022. During both deployments, tropopause-overshooting convection
> with water vapor and temperature conditions suitable for chlorine
> activation were sampled. Due to their relatively young chemical age, most
> of these cold and wet air masses had abundances of inorganic chlorine (Cly)
> too low to support eventual enhancements of ClO that would lead to
> widespread ozone depletion. Even in the few air masses with higher levels
> of Cly, the abundance of nitrogen oxides was elevated and the ratio of
> ClONO2 to Cly was observed to be very low, limiting the availability of
> ClONO2 to react with HCl and sustain chlorine activation. However, we show
> that for the average chemical and meteorological conditions of cold, wet,
> overshooting air parcels observed during DCOTSS, significant chlorine
> activation could occur if stratospheric sulfate SAD were enhanced by major
> volcanic eruptions or *climate intervention efforts.*
>
> *Plain Language Summary*
> Stratospheric ozone shields life on Earth from the Sun's harmful
> ultraviolet rays. Mixed-phase chemical reactions, which typically occur
> only at very low temperatures, produce large amounts of chlorine monoxide
> (ClO), a chemical that rapidly depletes stratospheric ozone. Previous
> studies have hypothesized that abundances of ClO, capable of leading to
> substantial ozone depletion, could be found in the midlatitude stratosphere
> when large storms inject water vapor high into the stratosphere. During the
> Dynamics and Chemistry of the Summer Stratosphere (DCOTSS) NASA ER-2
> aircraft field campaign, magnitudes of ClO capable of causing significant
> ozone depletion were not observed within cold and wet air masses. Although
> large amounts of water vapor were injected into the stratosphere by these
> storms, the air masses lacked the chemical conditions necessary for
> chlorine activation to cause significant ozone loss. Additionally, our
> modeling analysis of data collected during DCOTSS indicates that the
> stratospheric injection of sulfate, in an effort to mitigate global
> warming, could increase the risk of chlorine activation in the midlatitude
> lower stratosphere.
>
> *Key Points*
>
> Observations of ClO from the Dynamics and Chemistry of the Summer
> Stratosphere mission show no evidence of heterogeneous chlorine activation
>
> Chlorine activation was limited by the availability of inorganic chlorine
> and the partitioning between the two major chlorine reservoirs
>
> Enhancement of sulfate aerosol surface area would increase the potential
> for chlorine activation in the midlatitude stratosphere
>
> *Source: AGU*
>
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