Airborne nitrous oxide observations over the western Pacific Ocean: September October 1991

被引:12
作者
Collins, JE
Sachse, GW
Anderson, BE
Harriss, RC
Bartlett, KB
Sandholm, S
Wade, LO
Burney, LG
Hill, GF
机构
[1] NASA, LANGLEY RES CTR, DIV ATMOSPHER SCI, HAMPTON, VA 23681 USA
[2] UNIV NEW HAMPSHIRE, INST STUDY EARTH OCEANS & SPACE, DURHAM, NH 03824 USA
[3] NASA, LANGLEY RES CTR, DIV AEROSP ELECTR SYST, HAMPTON, VA 23681 USA
[4] GEORGIA INST TECHNOL, ATLANTA, GA 30332 USA
[5] LOCKHEED ENGN & SCI CO, HAMPTON, VA 23666 USA
关键词
D O I
10.1029/95JD02530
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
The Langley tunable diode laser instrument package incorporated an additional channel to measure nitrous oxide (N2O) during the Pacific Exploratory Mission (PEM) West A. These measurements represent the first airborne, fast response (5-s) N2O data set obtained within the troposphere, Most data were recorded over the western Pacific between 0 degrees N and 45 degrees N latitude, 110 degrees E and 180 degrees E longitude, and 0.3 to 12 km altitude. Important observations include a decreasing N2O latitude gradient of approximately 0.4 parts per billion volumn (ppbv) from northern midlatitudes to the equator, a decreasing N2O longitude gradient of 0.4 ppbv from the western Pacific to the central Pacific at northern midlatitudes, and an enhancement of 0.2 ppbv in the boundary layer (altitudes below 0.5 km) relative to the rest of the tropospheric vertical profile. Other observations include increased N2O mixing ratios within both urban and biogenic affected air masses and reduced N2O mixing ratios in stratospheric intrusions. These relationships with air mass source characteristics are exhibited in the large-scale correlations between N2O and CO, CH4, and CO2 in the free troposphere. Atmospheric inputs of N2O are examined and the relative strengths of continental biogenic and anthropogenic/industrial sources are estimated. The data set is also examined for evidence of an oceanic source of N2O.
引用
收藏
页码:1975 / 1984
页数:10
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