首页> 外文期刊>Journal of Geophysical Research. Biogeosciences >ATMOSPHERIC SULFUR CYCLING IN THE TROPICAL PACIFIC MARINE BOUNDARY LAYER (12-DEGREES-S,135-DEGREES-W) - A COMPARISON OF FIELD DATA AND MODEL RESULTS .2. SULFUR DIOXIDE
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ATMOSPHERIC SULFUR CYCLING IN THE TROPICAL PACIFIC MARINE BOUNDARY LAYER (12-DEGREES-S,135-DEGREES-W) - A COMPARISON OF FIELD DATA AND MODEL RESULTS .2. SULFUR DIOXIDE

机译:热带太平洋海洋边界层(12度-S,135度-W)中的大气硫循环-现场数据和模型结果的比较.2。二氧化硫

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The atmospheric chemistry of sulfur dioxide over the tropical South Pacific Ocean is investigated by using results from field measurements and numerical models. Simultaneous real time measurements of sulfur dioxide and its biogenic precursor dimethylsulfide were made at 12 degrees S, 135 degrees W for a 6-day period from March 3 through March 9, 1992. The mean SO:! and DMS mole fractions were 71 +/- 56 pmol mol(-1) (1 sigma) and 453 +/- 93 pmol mol(-1) (1 sigma) respectively. These concentrations are compared to those predicted by a time-dependent photochemical box model of the marine boundary layer. Model estimates of the yield of SO2 from DMS oxidation range from 27% to 54%. Even with low yields, DMS is the dominant source of SO2 in this region. Estimates of vertical entrainment velocities based on the tropospheric ozone budget suggest that vertical entrainment is a minor source of SO2. The relative rates of various loss mechanisms for SO2 are dry deposition to the sea surface (58%), in-cloud oxidation (9%), OH oxidation (5%), and uptake by sea-salt aerosols (28%). [References: 42]
机译:通过使用现场测量和数值模型研究了热带南太平洋上的二氧化硫的大气化学。从1992年3月3日到3月9日,在6天的时间里,同时在12°S,135°W下对二氧化硫及其生物前体二甲基硫醚进行了实时实时测量。和DMS摩尔分数分别为71 +/- 56 pmol mol(-1)(1 sigma)和453 +/- 93 pmol mol(-1)(1 sigma)。将这些浓度与海洋边界层的时间依赖性光化学盒模型所预测的浓度进行比较。 DMS氧化产生的SO2的模型估计范围为27%至54%。即使单产较低,DMS仍是该地区SO2的主要来源。根据对流层臭氧收支估算垂直夹带速度,表明垂直夹带是SO2的次要来源。 SO2各种损失机制的相对比率是:干沉积到海面(58%),云中氧化(9%),OH氧化(5%)和海盐气溶胶的吸收(28%)。 [参考:42]

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