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Vertical variations of sea-salt modification in the boundary layer of spring Arctic during the ASTAR 2000 campaign

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TAYLOR & FRANCIS LTD
DOI: 10.1034/j.1600-0889.2002.201253.x

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Airborne and ground-based aerosol/gas measurements were carried out in Svalbard between mid-March and mid-April 2000. From the viewpoint of vertical features of sea-salt modification in the lower troposphere (less than or equal to 1500 m) of the Arctic spring, more than 1000 individual sea-salt particles were analyzed with scanning electron microscopy energy dispersive X-ray spectrometry (SEM-EDX) in the present study. Individual particle analysis suggested a vertical gradient of sea-salt modification in fine sea-salt particles with an attitude of 59-1485 m above sea level (asl), e.g. chlorine liberation rates of 33.0% (212 m asl) and 81.0% (1266 m asl) on 15 March, and 72.7% (100 m asl), 83.8% (495 m asl) and 95.8% (1411 m asl) on 26 March. Sea salts may be dominantly modified with SO2 and SO42- under Arctic haze conditions with higher SO2 concentration (greater than or equal to 2 nmol m(-3)), whereas they are dominantly modified with NO3- and reactive nitrogen oxides under Arctic background conditions, with [HNO3] of 0.15-1.3 nmol m(-3) and [SO2] of 0.04-2 nmol m(-3). Vertical trends in sea-salt modification suggested that it makes a significant contribution to the formation of reactive halo.-en species in the upper boundary layer and the lower free troposphere of the spring Arctic.

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