In situ HNO3 to NOy instrument comparison during SOLVE -: art. no. 4188

被引:19
作者
Ballenthin, JO
Thorn, WF
Miller, TM
Viggiano, AA
Hunton, DE
Koike, M
Kondo, Y
Takegawa, N
Irie, H
Ikeda, H
机构
[1] USAF, Res Lab, Space Vehicles Directorate, VSBXT, Hanscom AFB, MA 01731 USA
[2] Univ Tokyo, Adv Sci & Technol Res Ctr, Meguro Ku, Tokyo 1538904, Japan
[3] Univ Tokyo, Grad Sch Sci, Dept Earth & Planetary Sci, Bunkyo Ku, Tokyo 1130033, Japan
[4] Natl Inst Environm Studies, Satellite Remote Sensing Res Team, Tsukuba, Ibaraki 3058506, Japan
关键词
nitric acid; reactive nitrogen; chemical ionization mass spectrometry; HNO3; NOy; instrumentation;
D O I
10.1029/2002JD002136
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
[1] Measurements of HNO3 mixing ratios from the chemical ionization mass spectrometer have been critically compared with simultaneous measurements of total gas phase NOy from the NO chemiluminescence detector aboard the NASA DC-8 aircraft during the SAGE 3 Ozone Loss and Validation Experiment (SOLVE). The data were obtained in the arctic upper troposphere and lower stratosphere in the winter of 1999-2000. A brief comparison to the NOy instrument aboard the NASA ER-2 is also presented. The time responses, detection limits, relative precision, and stability of relative calibrations for the instruments were in excellent agreement throughout the mission. However, the average slope of the HNO3 to NOy correlation was 1.13 +/- 0.03 overall and 1.06 +/- 0.03 in stratospheric air, indicating that the two measurements had a systematic calibration offset. Possible sources for the offset error are presented, and methods to reduce the calibration error in future flights are suggested.
引用
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页数:11
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