Synoptic tracer gradients in the upper troposphere over central Canada during the Stratosphere-Troposphere Experiments by Aircraft Measurements 1998 summer campaign

被引:15
作者
Fischer, H
Brunner, D
Harris, GW
Hoor, P
Lelieveld, J
McKenna, DS
Rudolph, J
Scheeren, HA
Siegmund, P
Wernli, H
Williams, J
Wong, S
机构
[1] Max Planck Inst Chem, D-55020 Mainz, Germany
[2] ETH Honggerberg, Swiss Fed Inst Technol, HPP, Inst Atmospher Sci, CH-8093 Zurich, Switzerland
[3] York Univ, Ctr Atmospher Chem, N York, ON M3J 1P3, Canada
[4] Natl Ctr Atmospher Res, Boulder, CO 80307 USA
[5] Univ Utrecht, Inst Marine & Atmospher Res, NL-3584 CC Utrecht, Netherlands
[6] Royal Netherlands Meteorol Inst, NL-3730 AE De Bilt, Netherlands
[7] Forschungszentrum, Julich, Germany
关键词
upper troposphere; chemical composition; stratosphere-troposphere exchange; airstreams; coherent trajectory ensembles;
D O I
10.1029/2000JD000312
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] During the July 1998 Stratosphere-Troposphere Experiments by Aircraft Measurements (STREAM) intensive campaign, eight measurement flights were conducted from Timmins airport (Ontario, Canada, 48.2degreesN, 79.3degreesW). In situ measurements of ozone, carbon monoxide, carbon dioxide, and nonmethane hydrocarbons, as well as three-dimensional back trajectories based on European Centre for Medium-Range Weather Forecasts wind field analyses, are used to characterize upper tropospheric air masses with respect to their origin. In the upper troposphere between 8 km and the local tropospause, about 40% of the air masses originated from the subtropics/tropics ksouth of 30degreesN, about 50% originated from midlatitudes (between 30degrees and 50degreesN), and 12% originated from the polar region north of 50degreesN. In general, highest trace gas levels were observed in air masses originating from midlatitudes (e. g., CO, 107 +/- 25 ppbv; ethane, 983 +/- 385 pptv; acetylene, 119 +/- 43 pptv), with the exception of CO, which had highest mixing ratios (121 +/- 11 ppbv) in air masses of polar origin. The lowest concentrations were generally observed in air masses of (sub) tropical origin (e. g., CO, 64 +/- 2 ppbv; ethane, 424 +/- 86 pptv; acetylene, 39 +/- 14 pptv). For CO and most of the alkanes a significant positive latitudinal gradient was observed, while CO2 and CH3Cl exhibited an inverse gradient with lowest mixing ratios at high northern latitudes. This reflects the different source and sink distributions of the investigated species. Ozone mixing ratios significantly increased in the upper troposphere above 8 km altitude, at least partially because of stratosphere-troposphere exchange. Approximately 10% of the upper tropospheric air was directly influenced by recent cross-tropopause exchange. A case study indicates that the convergence of air masses of different origin along a cold front creates sharp gradients not only in temperature and humidity but also in trace gas concentrations. It is shown that these mesoscale gradients result from the organized flows of tropical, arctic, and stratospheric air masses.
引用
收藏
页数:13
相关论文
共 46 条
[1]   STRATOSPHERIC/TROPOSPHERIC EXCHANGE AFFECTING THE NORTHERN WETLANDS REGIONS OF CANADA DURING SUMMER 1990 [J].
BACHMEIER, AS ;
SHIPHAM, MC ;
BROWELL, EV ;
GRANT, WB ;
KLASSA, JM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D1) :1793-1804
[2]   Chemical air mass differences near fronts [J].
Bethan, S ;
Vaughan, G ;
Gerbig, C ;
Volz-Thomas, A ;
Richer, H ;
Tiddeman, DA .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D11) :13413-13434
[3]  
Bjerknes P.V.F, 1910, Q J R METEOROL SOC, V36, P267, DOI [10.1002/qj.49703615505, DOI 10.1002/QJ.49703615505]
[4]   SUMMERTIME MEASUREMENTS OF SELECTED NONMETHANE HYDROCARBONS IN THE ARCTIC AND SUB-ARCTIC DURING THE 1988 ARCTIC BOUNDARY-LAYER EXPEDITION (ABLE-3A) [J].
BLAKE, DR ;
HURST, DF ;
SMITH, TW ;
WHIPPLE, WJ ;
CHEN, TY ;
BLAKE, NJ ;
ROWLAND, FS .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D15) :16559-16588
[5]   AIRCRAFT MEASUREMENTS OF O-3, HNO3 AND N2O IN THE WINTER ARCTIC LOWER STRATOSPHERE DURING THE STRATOSPHERE-TROPOSPHERE EXPERIMENT BY AIRCRAFT MEASUREMENTS (STREAM) .1. [J].
BREGMAN, A ;
VANVELTHOVEN, PFJ ;
WIENHOLD, FG ;
FISCHER, H ;
ZENKER, T ;
WAIBEL, A ;
FRENZEL, A ;
ARNOLD, F ;
HARRIS, GW ;
BOLDER, MJA ;
LELIEVELD, J .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1995, 100 (D6) :11245-11260
[6]   OZONE AND AEROSOL DISTRIBUTIONS IN THE SUMMERTIME TROPOSPHERE OVER CANADA [J].
BROWELL, EV ;
FENN, MA ;
BUTLER, CF ;
GRANT, WB ;
HARRISS, RC ;
SHIPHAM, MC .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D1) :1739-1755
[7]  
BROWNING KA, 1994, Q J ROY METEOR SOC, V120, P1535, DOI 10.1002/qj.49712052006
[8]  
BROWNING KA, 1990, EXTRATROPICAL CYCLONES, P129
[9]   GHOST - A novel airborne gas chromatograph for in situ measurements of long-lived tracers in the lower stratosphere: Method and applications [J].
Bujok, O ;
Tan, V ;
Klein, E ;
Nopper, R ;
Bauer, R ;
Engel, A ;
Gerhards, MT ;
Afchine, A ;
McKenna, DS ;
Schmidt, U ;
Wienhold, FG ;
Fischer, H .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2001, 39 (01) :37-64
[10]  
CARLSON TN, 1980, MON WEATHER REV, V108, P1498, DOI 10.1175/1520-0493(1980)108<1498:ATMCAT>2.0.CO