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Relationship between atmospheric CH 4 and the calculated sea-to-air CH 4 flux
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Abstract
Background
Effect of atmospheric CH4 mole fraction on sea-to-air CH4 flux was important for assessment of carbon emissions, while it was paid little attention and lack of quantification.
Results
According to the method described by Wanninkhof (2014), the impacts of three different atmospheric CH4 data on the calculated sea-to-air CH4 flux were evaluated. Results showed that, compared to data observed at the Tae-ahn Peninsula station and the simulated MBL-CH4 references, in situ observed atmospheric CH4 mole fraction was 132 and 140 nmol/mol higher in July 2013, and 98 and 132 nmol/mol higher in February 2017 in the Bohai Sea, respectively. The different applied atmospheric CH4 mole fraction induced mean deviations of 1.5 µmol/m2/day in July 2013 and 1.0 µmol/m2/day in February 2017, respectively. In addition, effects of difference among three atmospheric CH4 mole fractions could result in greater deviations of calculated sea-to-air CH4 flux in summer in coastal shallow waters than that in winter in deep regions or open oceans.
Conclusions
From the perspective of narrowing the uncertainty of carbon emission, it was essential to calculate sea-to-air CH4 flux by using the field observed atmospheric CH4 mole fraction, especially in coastal shallow seas.
Springer Science and Business Media LLC
Title: Relationship between atmospheric CH 4 and the calculated sea-to-air CH 4 flux
Description:
Abstract
Background
Effect of atmospheric CH4 mole fraction on sea-to-air CH4 flux was important for assessment of carbon emissions, while it was paid little attention and lack of quantification.
Results
According to the method described by Wanninkhof (2014), the impacts of three different atmospheric CH4 data on the calculated sea-to-air CH4 flux were evaluated.
Results showed that, compared to data observed at the Tae-ahn Peninsula station and the simulated MBL-CH4 references, in situ observed atmospheric CH4 mole fraction was 132 and 140 nmol/mol higher in July 2013, and 98 and 132 nmol/mol higher in February 2017 in the Bohai Sea, respectively.
The different applied atmospheric CH4 mole fraction induced mean deviations of 1.
5 µmol/m2/day in July 2013 and 1.
0 µmol/m2/day in February 2017, respectively.
In addition, effects of difference among three atmospheric CH4 mole fractions could result in greater deviations of calculated sea-to-air CH4 flux in summer in coastal shallow waters than that in winter in deep regions or open oceans.
Conclusions
From the perspective of narrowing the uncertainty of carbon emission, it was essential to calculate sea-to-air CH4 flux by using the field observed atmospheric CH4 mole fraction, especially in coastal shallow seas.
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