The good news comes from NASA published at Science Daily Greenhouse gas ‘detergent’ recycles itself in atmosphere. The study explains how the atmosphere functions as a methane sink, and why the process is resilient and handles whatever CH4 is emitted. Scientists had worried that the atmospheric capacity to wash away methane might decay over time, but that fear turns out to be unfounded. Excerpts in italics with my bolds.
A simple molecule in the atmosphere that acts as a ‘detergent’ to break down methane and other greenhouse gases has been found to recycle itself to maintain a steady global presence in the face of rising emissions, according to new research. Understanding its role in the atmosphere is critical for determining the lifetime of methane, a powerful contributor to climate change.
The hydroxyl (OH) radical, a molecule made up of one hydrogen atom, one oxygen atom with a free (or unpaired) electron is one of the most reactive gases in the atmosphere and regularly breaks down other gases, effectively ending their lifetimes. In this way OH is the main check on the concentration of methane, a potent greenhouse gas that is second only to carbon dioxide in contributing to increasing global temperatures.
With the rise of methane emissions into the atmosphere, scientists historically thought that might cause the amount of hydroxyl radicals to be used up on the global scale and, as a result, extend methane’s lifetime, currently estimated to be nine years. However, in addition to looking globally at primary sources of OH and the amount of methane and other gases it breaks down, this new research takes into account secondary OH sources, recycling that happens after OH breaks down methane and reforms in the presence of other gases, which has been observed on regional scales before.
“OH concentrations are pretty stable over time,” said atmospheric chemist and lead author Julie Nicely at NASA’s Goddard Space Flight Center in Greenbelt, Maryland. “When OH reacts with methane it doesn’t necessarily go away in the presence of other gases, especially nitrogen oxides (NO and NO2). The break down products of its reaction with methane react with NO or NO2 to reform OH. So OH can recycle back into the atmosphere.”
OH in the atmosphere also forms when ultraviolet sunlight reaches the lower atmosphere and reacts with water vapor (H2O) and ozone (O3) to form two OH molecules. Over the tropics, water vapor and ultraviolet sunlight are plentiful. The tropics, which span the region of Earth to either side of the equator, have shown some evidence of widening farther north and south of their current range, possibly due to rising temperatures affecting air circulation patterns. This means that the tropical region primed for creating OH will potentially increase over time, leading to a higher amount of OH in the atmosphere. This tropical widening process is slow, however, expanding only 0.5 to 1 degree in latitude every 10 years. But the small effect may still be important, according to Nicely.
She and her team found that, individually, the tropical widening effect and OH recycling through reactions with other gases each comprise a relatively small source of OH, but together they essentially replace the OH used up in the breaking down of methane.
“The absence of a trend in global OH is surprising,” said atmospheric chemist Tom Hanisco at Goddard who was not involved in the research. “Most models predict a ‘feedback effect’ between OH and methane. In the reaction of OH with methane, OH is also removed. The increase in NO2 and other sources of OH, such as ozone, cancel out this expected effect.” But since this study looks at the past thirty-five years, it’s not guaranteed that as the atmosphere continues to evolve with global climate change that OH levels will continue to recycle in the same way into the future, he said.
Ultimately, Nicely views the results as a way to fine-tune and update the assumptions that are made by researchers and climate modelers who describe and predict how OH and methane interact throughout the atmosphere. “This could add clarification on the question of will methane concentrations continue rising in the future? Or will they level off, or perhaps even decrease? This is a major question regarding future climate that we really don’t know the answer to,” she said.
Abstract from AGU publication Changes in Global Tropospheric OH Expected as a Result of Climate Change Over the Last Several Decades Julie M. Nicely
The oxidizing capacity of the troposphere is controlled primarily by the abundance of hydroxyl radical (OH). The global mean concentration of tropospheric OH, [OH]TROP (the burden of OH in the global troposphere appropriate for calculating the lifetime of methane) inferred from measurements of methyl chloroform has remained relatively constant during the past several decades despite rising levels of methane that should have led to a decline.
Here we examine other factors that may have affected [OH]TROP such as the changing values of stratospheric ozone, rising tropospheric H2O, varying burden of NOx (=NO+NO2), rising temperatures, and widening of the climatological tropics due to expansion of the Hadley cell. Our analysis suggests the positive trends in [OH]TROP due to H2O, NOx, and overhead O3, and tropical expansion are large enough (Δ [OH]TROP = +0.95 ± 0.18%/decade) to counter almost all of the expected decrease in [OH]TROP due to rising methane (Δ [OH]TROP = −1.01 ± 0.05%/decade) over the period 1980 to 2015, while variations in temperature contribute almost no trend (Δ [OH]TROP = −0.02 ± 0.02%/decade) in [OH]TROP. The approximated impact of Hadley cell expansion on [OH]TROP is also a small but not insignificant factor partially responsible for the steadiness of tropospheric oxidizing capacity over the past several decades, which free‐running models likely do not capture.