Atmospheric research program for studying changing emission patterns after German unification

被引:22
|
作者
Acker, K
Moller, D
Marquardt, W
Bruggemann, E
Wieprecht, W
Auel, R
Kalass, D
机构
[1] Brandenburg Tech Univ Cottbus, Working Grp Air Chem, D-12484 Berlin, Germany
[2] Inst Tropospher Res IFT, D-04303 Leipzig, Germany
关键词
emission; trend; precipitation chemistry; cloud chemistry;
D O I
10.1016/S1352-2310(98)00041-7
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A dramatic decrease in emission of sulphur dioxide (SO(2), 60%), dust (82%), nitrogen oxide (NO, 30%) and other pollutants (hydrochloric acid (HCl); ammonia (NH(3))) has been observed in East Germany after German unification in 1989. The smaller decrease in total NO is due to significant increase of NO from traffic. Air-pollutant concentrations in both parts of Germany before and after 1989 will be compared and their development will be discussed, based on precipitation and cloud chemistry data from long-term continuous record. Sectoral rain data, based on backward trajectory calculations, clearly show that the significant decline in annual volume weighted precipitation ions (sulphate, calcium, ammonium,chloride) in rain water from sector "East" since 1989 and particularly since about 1992 is roughly correlated with a similar percentage decline in SO(2), dust and NH(3) emissions for the region East Germany. The acidity of the precipitation from sector "East" has increased very strikingly from 1993 up to 1995 threefold more than from sector "West". Despite the strong decrease in SO(2) emission, this decrease of the atmospheric neutralising capacity was caused by the much steeper decline in atmospheric base cations in that region. Precipitation data from all transport directions show high variation, but no significant trend in the annual average H(+) ion concentration. At Mt. Brocken the annual average volume weighted cloud-water acidity during frost-free periods increased by a factor of three between 1992 and 1995. This result, confirmed also by the annual frequency distributions of the pH values, reflects the atmospheric pollutant loading also from all entry sectors. After 1995 this trend is reversed. Detailed classification of the cloud-water data by entry sector, and by meteorological and especially microphysical factors is currently being carried out and preliminary results are presented. (C) 1998 Elsevier Science Ltd. All rights reserved.
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页码:3435 / 3443
页数:9
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