Hydrogen peroxide in the marine atmospheric boundary layer during the Atlantic Stratocumulus Transition Experiment/ Marine Aerosol and Gas Exchange experiment in the eastern subtropical North Atlantic

International audience Gas phase H20 2 was measured in surface air on the NOAA ship Malcolm Baldrige from June 8 to 27, 1992 (Julian days 160-179), during the Atlantic Stratocumulus Transition Experiment/Marine Aerosol and Gas Exchange experiment in the eastern subtropical North Atlantic region. Ave...

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Bibliographic Details
Published in:Journal of Geophysical Research: Atmospheres
Main Authors: Martin, Daniel, Tsivou, Maria, Bonsang, Bernard, Abonnel, Christian, Carsey, Thomas, Springer-Young, Margie, Pszenny, Alex, Suhre, Karsten
Other Authors: Centre des Faibles Radioactivités, Centre National de la Recherche Scientifique (CNRS)-Commissariat à l'énergie atomique et aux énergies alternatives (CEA)
Format: Article in Journal/Newspaper
Language:English
Published: HAL CCSD 1997
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Online Access:https://hal.archives-ouvertes.fr/hal-03357865
https://hal.archives-ouvertes.fr/hal-03357865/document
https://hal.archives-ouvertes.fr/hal-03357865/file/96JD03056.pdf
https://doi.org/10.1029/96JD03056
Description
Summary:International audience Gas phase H20 2 was measured in surface air on the NOAA ship Malcolm Baldrige from June 8 to 27, 1992 (Julian days 160-179), during the Atlantic Stratocumulus Transition Experiment/Marine Aerosol and Gas Exchange experiment in the eastern subtropical North Atlantic region. Average H20 2 mixing ratios observed were 0.63 _+ 0.28 ppbv, ranging between detection limit and 1.5 ppbv. For the entire experiment, only weak or no correlation was found between H20 2 mixing ratio and meteorological parameters (pressure, temperature, humidity, or UV radiation flux) as well as with tracers of continental air masses (CO, black carbon, radon). The average daily H20 2 cycle for the entire period exhibits a maximum of 0.8 _+ 0.3 ppbv near sunset and a minimum of 0.4 _+ 0.2 ppbv 4-5 hours after sunrise. Several clear H20 2 diurnal variations have been observed, from which a first-order removal rate of about 1 x 10-s s-• for H20 2 can be inferred from nighttime measurements. This rate compares well with those deduced from measurements taken at Cape Grim (Tasmania, 41øS) and during the Soviet-American Gas and Aerosol III experiment (equatorial Pacific Ocean).