A comparison of aircraft and ground-based measurements at Mauna Loa observatory, Hawaii, during GTE PEM-west and MLOPEX 2

被引:7
作者
Atlas, E
Ridley, B
Walega, J
Greenberg, J
Kok, G
Staffelbach, T
Schauffler, S
Lind, J
Hubler, G
Norton, R
Liu, S
Davis, D
Bandy, A
Blake, D
Bradshaw, J
Browell, E
Collins, JE
Gregory, G
Heikes, B
Kondo, Y
Sachse, G
Sandholm, S
Singh, H
Talbot, B
Dlugokencky, E
Elkins, J
Oltmans, S
Mackay, G
Karecki, D
机构
[1] DREXEL UNIV, DEPT CHEM, PHILADELPHIA, PA 19104 USA
[2] UNIV CALIF IRVINE, DEPT CHEM, IRVINE, CA 92717 USA
[3] GEORGIA INST TECHNOL, ATLANTA, GA 30332 USA
[4] NASA, LANGLEY RES CTR, HAMPTON, VA 23681 USA
[5] NOAA, CLIMATE MONITORING & DIAGNOST LAB, BOULDER, CO 80303 USA
[6] UNIV RHODE ISL, GRAD SCH OCEANOG, NARRAGANSETT, RI 02882 USA
[7] NOAA, AERON LAB, BOULDER, CO 80303 USA
[8] UNISEARCH ASSOCIATES, CONCORD, ON L4K 1B5, CANADA
[9] NAGOYA UNIV, SOLAR TERR ENVIRONM LAB, TOYOKAWA, AICHI 442, JAPAN
[10] NASA, AMES RES CTR, MOFFETT FIELD, CA 94035 USA
[11] UNIV NEW HAMPSHIRE, COMPLEX SYST RES CTR, INST EARTH OCEANS & SPACE, DURHAM, NH 03824 USA
关键词
D O I
10.1029/96JD00213
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
During October 19-20, 1991, one flight of the NASA Global Tropospheric Experiment (GTE) Pacific Exploratory Mission (PEM-West A) mission was conducted near Hawaii as an intercomparison with ground-based measurements of the Mauna Loa Observatory Photochemistry Experiment (MLOPEX 2) and the NOAA Climate Modeling and Diagnostics Laboratory (CMDL). Ozone, reactive nitrogen species, peroxides, hydrocarbons, and halogenated hydrocarbons were measured by investigators aboard the DC-8 aircraft and at the ground site. Lidar cross sections of ozone revealed a complex air mass structure near the island of Hawaii which was evidenced by large variation in some trace gas mixing ratios. This variation limited the time and spatial scales for direct measurement intercomparisons. Where differences occurred between measurements in the same air masses, the intercomparison suggested that biases for some trace gases was due to different calibration scales or, in some cases, instrumental or sampling biases. Relatively large uncertainties were associated with those trace gases present in the low parts per trillion by volume range. Trace gas correlations were used to expand the scope of the intercomparison to identify consistent trends between the different data sets.
引用
收藏
页码:14599 / 14612
页数:14
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