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Amplified trace gas removal in the troposphere.

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TLDR
Concentrations of OH were three to five times greater than expected, and the existence of a pathway for the regeneration of OH independent of NO is proposed, which amplifies the degradation of pollutants without producing ozone.
Abstract
The degradation of trace gases and pollutants in the troposphere is dominated by their reaction with hydroxyl radicals (OH). The importance of OH rests on its high reactivity, its ubiquitous photochemical production in the sunlit atmosphere, and most importantly on its regeneration in the oxidation chain of the trace gases. In the current understanding, the recycling of OH proceeds through HO2 reacting with NO, thereby forming ozone. A recent field campaign in the Pearl River Delta, China, quantified tropospheric OH and HO2 concentrations and turnover rates by direct measurements. We report that concentrations of OH were three to five times greater than expected, and we propose the existence of a pathway for the regeneration of OH independent of NO, which amplifies the degradation of pollutants without producing ozone.

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Journal ArticleDOI

Atmospheric composition change – global and regional air quality

Paul S. Monks, +68 more
TL;DR: A review of the state of scientific understanding in relation to global and regional air quality is outlined in this article, in terms of emissions, processing and transport of trace gases and aerosols.
Journal ArticleDOI

Multiphase chemistry at the atmosphere-biosphere interface influencing climate and public health in the anthropocene.

TL;DR: This work addresses air contaminants and their multiphase chemical interactions at the atmosphere−biosphere interface, including human lungs and skin, plant leaves, cryptogamic covers, soil, and aquatic surfaces, and the chemical interactions of reactive oxygen species and reactive nitrogen species, as well as carbonaceous combustion aerosols.
Journal ArticleDOI

Tropospheric OH and HO2 radicals: field measurements and model comparisons.

TL;DR: This critical review discusses field measurements of local concentrations of OH and HO(2) radicals in the troposphere, and in particular the comparisons that have been made with numerical model calculations containing a detailed chemical mechanism.
References
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Journal ArticleDOI

Known and unexplored organic constituents in the Earth's atmosphere

TL;DR: The sources, structure, chemistry, and fate of gas-phase and aerosol organic compounds were studied in this article. But much remains to be learned about the sources, structures, and chemistry of these compounds.
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Ozone production in the rural troposphere and the implications for regional and global ozone distributions

TL;DR: The relationship between O3 and NOx (NO + NO2) which was measured during summer and winter periods at Niwot Ridge, Colorado, has been analyzed and compared to model calculations.
Journal ArticleDOI

Normal atmosphere: large radical and formaldehyde concentrations predicted.

TL;DR: A radical chain reaction is proposed for the rapid removal of carbon monoxide, leading to acarbon monoxide lifetime as low as 0.2 year in the surface atmosphere.
Journal ArticleDOI

Atmospheric oxidation capacity sustained by a tropical forest

TL;DR: It is proposed that natural VOC oxidation, notably of isoprene, recycles OH efficiently in low-NOx air through reactions of organic peroxy radicals, which demonstrates that the biosphere maintains a remarkable balance with the atmospheric environment.
Journal ArticleDOI

Missing OH reactivity in a forest: evidence for unknown reactive biogenic VOCs.

TL;DR: In a northern Michigan forest, the direct measurement of total OH reactivity, which is the inverse of the OH lifetime, was significantly greater than expected, consistent with the hypothesis that unknown reactive BVOCs, perhaps terpenes, provide the missingOH reactivity.
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