USE OF BACKWARD TRAJECTORIES TO INTERPRET THE 5-YEAR RECORD OF PAN AND O-3 AMBIENT AIR CONCENTRATIONS AT KEJIMKUJIK NATIONAL-PARK, NOVA-SCOTIA

被引:173
作者
SIROIS, A
BOTTENHEIM, JW
机构
关键词
D O I
10.1029/94JD02951
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Air parcel trajectory data are used in two ways to elucidate the temporal trend analysis of 5 years of peroxyacetyl nitrate (PAN) and O-3 Observations at a rural site in eastern Canada. In the first method, ''probability of residence'' contours are constructed to determine the most probable origin of air parcels containing the highest and lowest 10% of PAN and O-3 mixing ratios. High PAN is found to emanate always from areas of high anthropogenic activity, except when the transport path is to a large extent over the ocean, especially in the summer. High O-3 originates from the same regions except in the winter when because of low photochemical activity, O-3 is actually titrated and air from less populated areas is richer in O-3. The trajectories indicate that transport at higher altitude leads to higher mixing ratios; this is especially the case for O-3 in winter and spring. The complementary method of clustering the trajectories has allowed qualitative derivation of seasonal cycles for background and polluted air masses of different origin. Background air from the north shows a distinct PAN maximum in March; it is discussed that this could be either due to enhanced photochemistry or to the import of polluted air from the Arctic. Polluted air masses show the same March peak, but a second peak in late summer/early fall. Oceanic air from the south has a January maximum in PAN but otherwise is consistently low in PAN. O-3 also has a spring maximum, but in polluted air it is broader stretching into the summer. It is postulated that this is due to additional O-3 formation in the summer, while in the winter, actual O-3 loss is indicated for polluted air. By inference it is deduced that the second PAN peak in polluted air is also due to additional formation in comparison with background air, while in the summer, extra PAN loss mechanisms operate that are less important for O-3. Indications for both dry deposition and thermal decomposition have been found.
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页码:2867 / 2881
页数:15
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共 42 条
[2]   A STATISTICAL TRAJECTORY TECHNIQUE FOR DETERMINING AIR-POLLUTION SOURCE REGIONS [J].
ASHBAUGH, LL .
JOURNAL OF THE AIR POLLUTION CONTROL ASSOCIATION, 1983, 33 (11) :1096-1098
[3]   BACKGROUND POLLUTION IN THE ARCTIC AIR-MASS AND ITS RELEVANCE TO NORTH-AMERICAN ACID-RAIN STUDIES [J].
BARRIE, LA .
WATER AIR AND SOIL POLLUTION, 1986, 30 (3-4) :765-777
[4]   ESTIMATE OF OZONE PRODUCTION AND DESTRUCTION OVER NORTHWESTERN EUROPE [J].
BECK, JP ;
GRENNFELT, P .
ATMOSPHERIC ENVIRONMENT, 1994, 28 (01) :129-140
[5]  
BOJKOV RD, 1987, TROPOSPHERIC OZONE, P83
[6]   NONMETHANE HYDROCARBONS IN AN OCEANIC ATMOSPHERE [J].
BONSANG, B ;
LAMBERT, G .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1985, 2 (03) :257-271
[7]   Five years of continuous observations of PAN and ozone at a rural location in eastern Canada [J].
Bottenheim, Jan W. ;
Sirois, Alain ;
Brice, Kenneth A. ;
Gallant, Alan J. .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D3) :5333-5352
[8]   THE PARTITIONING OF NITROGEN-OXIDES IN THE LOWER ARCTIC TROPOSPHERE DURING SPRING 1988 [J].
BOTTENHEIM, JW ;
BARRIE, LA ;
ATLAS, E .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1993, 17 (01) :15-27
[9]  
BOTTENHEIM JW, 1994, IN PRESS ATMOS ENV
[10]   ATMOSPHERIC MEASUREMENTS OF PEROXYACETYLNITRATE (PAN) IN RURAL, SOUTHEAST ENGLAND - SEASONAL-VARIATIONS WINTER PHOTOCHEMISTRY AND LONG-RANGE TRANSPORT [J].
BRICE, KA ;
PENKETT, SA ;
ATKINS, DHF ;
SANDALLS, FJ ;
BAMBER, DJ ;
TUCK, AF ;
VAUGHAN, G .
ATMOSPHERIC ENVIRONMENT, 1984, 18 (12) :2691-2702