Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014

The oxidizing capacity of the atmosphere, or the ability of the atmosphere to clean itself of the pollutants that build up in the troposphere, is determined by oxidants including ozone (O₃), HOx radicals (OH and HO₂) and hydrogen peroxide (H₂O₂). O₃ is the primary source for HOx radicals, while H₂O₂...

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Main Author: Sun, Vanessa
Other Authors: Fiore, Arlene
Format: Thesis
Published: Massachusetts Institute of Technology 2024
Online Access:https://hdl.handle.net/1721.1/156613
https://orcid.org/0000-0001-5939-3468
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author Sun, Vanessa
author2 Fiore, Arlene
author_facet Fiore, Arlene
Sun, Vanessa
author_sort Sun, Vanessa
collection MIT
description The oxidizing capacity of the atmosphere, or the ability of the atmosphere to clean itself of the pollutants that build up in the troposphere, is determined by oxidants including ozone (O₃), HOx radicals (OH and HO₂) and hydrogen peroxide (H₂O₂). O₃ is the primary source for HOx radicals, while H₂O₂ is a key sink for HOx radicals that terminates the rapid cycling between OH and HO₂. The concentrations of the HOx radicals and H₂O₂ are difficult to measure directly, with scarce long term data of H₂O₂ primarily available through ice core records. Given the lack of observational data, much of our knowledge on the history of tropospheric oxidants relies on modeling studies. We quantify the global H₂O₂ burden and trends between 1950 and 2014 from the Community Earth System Model - Whole Atmosphere Community Climate Model version 6 (CESM2-WACCM6). This is a global chemistry-climate model, with each of the 13 ensemble members simulating the historical period. Each has a miniscule difference in their initial conditions, and subsequently yield different responses when reacting to the same external forcing. In this study, we discern where H₂O₂ is increasing in the troposphere, particularly in the Southern Hemisphere and over Antarctica. We quantify a rate of increase for the H₂O₂ annual burden, noting the rise beginning in the 1970's and growing from 14% in the 1970's to 34% in the 2000's, with respect to the burden in the 1950's. We find that changes in globally averaged annual mean H₂O₂ are most strongly correlated with changes in ozone, whereas over Antarctica, the strongest relationships for H₂O₂ trends occur with ozone photolysis rates. This aligns well with previous ice core and modelling studies in the literature. Lastly, we also find evidence of stratospheric ozone depletion having no discernible impact on global H₂O₂ burden changes using an additional parallel set of simulations holding ozone depleting substances at 1950 levels.
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spelling mit-1721.1/1566132024-09-04T03:17:27Z Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014 Sun, Vanessa Fiore, Arlene Massachusetts Institute of Technology. Department of Earth, Atmospheric, and Planetary Sciences The oxidizing capacity of the atmosphere, or the ability of the atmosphere to clean itself of the pollutants that build up in the troposphere, is determined by oxidants including ozone (O₃), HOx radicals (OH and HO₂) and hydrogen peroxide (H₂O₂). O₃ is the primary source for HOx radicals, while H₂O₂ is a key sink for HOx radicals that terminates the rapid cycling between OH and HO₂. The concentrations of the HOx radicals and H₂O₂ are difficult to measure directly, with scarce long term data of H₂O₂ primarily available through ice core records. Given the lack of observational data, much of our knowledge on the history of tropospheric oxidants relies on modeling studies. We quantify the global H₂O₂ burden and trends between 1950 and 2014 from the Community Earth System Model - Whole Atmosphere Community Climate Model version 6 (CESM2-WACCM6). This is a global chemistry-climate model, with each of the 13 ensemble members simulating the historical period. Each has a miniscule difference in their initial conditions, and subsequently yield different responses when reacting to the same external forcing. In this study, we discern where H₂O₂ is increasing in the troposphere, particularly in the Southern Hemisphere and over Antarctica. We quantify a rate of increase for the H₂O₂ annual burden, noting the rise beginning in the 1970's and growing from 14% in the 1970's to 34% in the 2000's, with respect to the burden in the 1950's. We find that changes in globally averaged annual mean H₂O₂ are most strongly correlated with changes in ozone, whereas over Antarctica, the strongest relationships for H₂O₂ trends occur with ozone photolysis rates. This aligns well with previous ice core and modelling studies in the literature. Lastly, we also find evidence of stratospheric ozone depletion having no discernible impact on global H₂O₂ burden changes using an additional parallel set of simulations holding ozone depleting substances at 1950 levels. S.M. 2024-09-03T21:11:47Z 2024-09-03T21:11:47Z 2024-05 2024-08-16T15:07:33.858Z Thesis https://hdl.handle.net/1721.1/156613 https://orcid.org/0000-0001-5939-3468 In Copyright - Educational Use Permitted Copyright retained by author(s) https://rightsstatements.org/page/InC-EDU/1.0/ application/pdf Massachusetts Institute of Technology
spellingShingle Sun, Vanessa
Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title_full Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title_fullStr Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title_full_unstemmed Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title_short Investigating Tropospheric Hydrogen Peroxide Trends from 1950-2014
title_sort investigating tropospheric hydrogen peroxide trends from 1950 2014
url https://hdl.handle.net/1721.1/156613
https://orcid.org/0000-0001-5939-3468
work_keys_str_mv AT sunvanessa investigatingtropospherichydrogenperoxidetrendsfrom19502014