Atmospheric trace gas measurements during SEEDS-II over the northwestern pacific |
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Affiliation: | 1. Lanzhou University, Key Laboratory for Environmental Pollution Prediction and Control, College of Earth and Environmental Sciences, Lanzhou, Gansu Province, China;2. Laboratory for Earth Surface Processes, College of Urban and Environmental Science, Peking University, Beijing, China;3. CAS Center for Excellence in Tibetan Plateau Earth Sciences, Chinese Academy of Sciences, Beijing, China |
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Abstract: | Atmospheric trace gas measurements were conducted during SEEDS-II. Atmospheric dimethylsulfide (DMS) was continuously measured by GC-MS during the R/V Hakuho cruise. Further, ambient air was sampled into canisters (42 samples) and analyzed by GC-MS and GC-FID for various biogenic and anthropogenic volatile organic compounds (VOCs) after the cruise. CO, O3, SO2, and NOx were monitored continuously aboard the ship.A fertilization experiment was conducted in a high-nitrate, low-chlorophyll (HNLC) region (48°N, 165°E). The atmospheric concentrations inside a patch (fertilized area) were compared with those outside it (natural area); however, clear differences were not observed for biogenic trace gasses (DMS, CH3Cl, CH3I, isoprene, and alkenes) in the atmosphere. However, a high DMS concentration was observed over the northwestern Pacific Ocean. The fertilized area was also observed by R/V Kilo Moana, and DMS was measured by GC-FPD. A good agreement was observed between the results of the measurements made aboard the two independent ships by different measurement methods.The atmospheric SO2 concentration was compared with the atmospheric DMS concentration. The SO2 concentration was found to vary with the atmospheric DMS concentration. A diurnal variation of the atmospheric DMS concentration was observed around the fertilized region. The DMS content tends to increase during the night and decrease during the day. A box model calculation was conducted to explain the diurnal variation of the atmospheric DMS. Since there was no diurnal variation of the wind speed, a constant DMS flux from the ocean surface was assumed. Further, the atmospheric OH radical concentration was assumed to be dependent on sunlight. The box model can roughly reproduce the atmospheric DMS diurnal variation mainly caused by its removal reaction with OH radicals. |
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