.png){kind=icon}
.png){kind=icon}
Return
Climate and Tropospheric Oxidizing Capacity
.png){kind=icon}
PRE
AI
A
L
Q
C
DOI：10.1146/annurev-earth-032320-090307.png)
.png){kind=icon}
Original request for help.png){kind=icon}
Share.png){kind=icon}
Save
Abstract
En 中文
The hydroxyl radical (OH) largely controls the tropospheric self-cleansing capacity by reacting with gases harmful to the environment and human health. OH concentrations are determined locally by competing production and loss processes. Lacking strong observational constraints, models differ in how they balance these processes, such that the sign of past and future OH changes is uncertain. In a warmer climate, OH production will increase due to its water vapor dependence, partially offset by faster OH-methane loss. Weather-sensitive emissions will also likely increase, although their net impact on global mean OH depends on the balance between source (nitrogen oxides) and sink (reactive carbon) gases. Lightning activity increases OH, but its response to climate warming is of uncertain sign. To enable confident projections of OH, we recommend efforts to reduce uncertainties in kinetic reactions, in measured and modeled OH, in proxies for past OH concentrations, and in source and sink gas emissions. OH is strongly modulated by internal climate variability despite its lifetime of a few seconds at most, with implications for interpreting trends in methane. Improved kinetic constraints on key reactions would strengthen confidence in regional and global OH budgets, and in the response of OH to climate change. Future OH changes will depend on uncertain and compensating processes involving weather-sensitive chemistry and emissions, plus human choices. Technological solutions to climate change will likely impact tropospheric oxidizing capacity and merit further study prior to implementation.
Keywords:
atmosphere
tropospheric chemistry
oxidation
hydroxyl radical
methane
Journal
IF:
13
Papers:
899
Citations:
1.1W
Organization
Cited Papers