Resolving the long-term trends of polycyclic aromatic hydrocarbons in the Canadian Arctic atmosphere

被引:52
作者
Becker, Sara
Halsall, Crispin J. [1 ]
Tych, Wlodek
Hung, Hayley
Attewell, Susie
Blanchard, Pierrette
Li, Henrik
Fellin, Phil
Stern, Gary
Billeck, Brian
Friesen, Sheri
机构
[1] Univ Lancaster, Lancaster Environm Ctr, Dept Environm Sci, Lancaster LA1 4YQ, England
[2] Meteorol Serv Canada, Toronto, ON M3H 5T4, Canada
[3] Air Zone, Mississauga, ON L5K 1A9, Canada
[4] Fisheries & Oceans Canada, Inst Freshwater, Dept Fisheries & Oceans, Winnipeg, MB R3T 2N6, Canada
关键词
D O I
10.1021/es052346l
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Polycyclic aromatic hydrocarbon (PAH) air concentrations measured over the period 1992-2000 at the Canadian High Arctic station of Alert were subject to time-series analysis using dynamic harmonic regression (DHR). For most of the PAHs, the DHR model fit to the observed data was good, with DHR capable of interpolating over missing data points during periods when air concentrations were below detection limits. As expected, DHR identified seasonal increases in PAH air concentrations. However, it has also identified additional, subtler "seasonal" patterns as a series of harmonics with varying periodicity. For example, a regular summer high in air concentrations was apparent for many PAHs, particularly the lower molecular weight (two- to three-ringed) compounds, which may be attributed to summertime regional combustion events such as forest fires and/or revolatilization from surfaces (e.g., soil and oceans, as well as arctic surfaces). Comparison of wintertime PAH concentrations (where Sigma PAH ranged from 260 to 516 pg m(-3)) with an earlier arctic study did not reveal a reduction in PAH levels. However, removal of the seasonal components by DHR revealed a declining trend in PAH concentrations over the 1992-2000 period. For many lighter PAHs, this was typified by a linear decrease over the whole time series, although, for the higher molecular weight PAHs, a marked reduction was apparent in the first few years of sampling followed by a leveling off in concentrations by the mid/late-1990s. This behavior is similar to reported trends of other air pollutants in the Arctic, may be attributed to the decline in Soviet industry during the early 1990s, and has implications regarding the major PAH sources affecting the Arctic.
引用
收藏
页码:3217 / 3222
页数:6
相关论文
共 34 条
[1]  
[Anonymous], 2004, AMAP Assessment 2002: Persistent Organic Pollutants in the Arctic
[2]   ARCTIC AIR-POLLUTION AND HUMAN HEALTH - WHAT EFFECTS SHOULD BE EXPECTED [J].
AYOTTE, P ;
DEWAILLY, E ;
BRUNEAU, S ;
CAREAU, H ;
VEZINA, A .
SCIENCE OF THE TOTAL ENVIRONMENT, 1995, 160-61 :529-537
[3]   Atmospheric organochlorine pesticides in the western Canadian Arctic: Evidence of transpacific transport [J].
Bailey, R ;
Barrie, LA ;
Halsall, CJ ;
Fellin, P ;
Muir, DCG .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2000, 105 (D9) :11805-11811
[4]  
BEA SY, 2002, ATMOS ENVIRON, V36, P5491
[5]  
*COMM EUR COMM, 2003, 20030164 COM COD COM
[6]   Temporal trends, temperature dependence, and relative reactivity of atmospheric polycyclic aromatic hydrocarbons [J].
Dimashki, M ;
Lim, LH ;
Harrison, RM ;
Harrad, S .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 2001, 35 (11) :2264-2267
[7]   Baseline contamination assessment for a new resource facility in Germany .6. Levels and profiles of polycyclic aromatic hydrocarbons (PAH) in ambient air [J].
Dorr, G ;
Hippelein, M ;
Kaupp, H ;
Hutzinger, O .
CHEMOSPHERE, 1996, 33 (08) :1569-1578
[8]   WOOD-BURNING AS A SOURCE OF ATMOSPHERIC POLYCYCLIC AROMATIC-HYDROCARBONS [J].
FREEMAN, DJ ;
CATTELL, FCR .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1990, 24 (10) :1581-1585
[9]   Trends of heavy metal components in the Arctic aerosols and their relationship to the emissions in the Northern Hemisphere [J].
Gong, SL ;
Barrie, LA .
SCIENCE OF THE TOTAL ENVIRONMENT, 2005, 342 (1-3) :175-183
[10]   Particle-associated polycyclic aromatic hydrocarbons in urban air of Hong Kong [J].
Guo, H ;
Lee, SC ;
Ho, KF ;
Wang, XM ;
Zou, SC .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (38) :5307-5317