Formaldehyde over the central Pacific during PEM-Tropics B

被引:32
作者
Heikes, B [1 ]
Snow, J
Egli, P
O'Sullivan, D
Crawford, J
Olson, J
Chen, G
Davis, D
Blake, N
Blake, D
机构
[1] Univ Rhode Isl, Grad Sch Oceanog, Ctr Atmospher Chem Studies, Narragansett, RI 02882 USA
[2] USN Acad, Dept Chem, Annapolis, MD 21402 USA
[3] NASA, Langley Res Ctr, Div Atmospher Sci, Hampton, VA 23681 USA
[4] Georgia Inst Technol, Sch Earth & Atmospher Sci, Atlanta, GA 30332 USA
[5] Univ Calif Irvine, Dept Chem, Irvine, CA 92717 USA
[6] Univ New Hampshire, Dept Chem, Durham, NH 03824 USA
关键词
D O I
10.1029/2001JD900012
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Formaldehyde, CH2O, mixing ratios are reported for the central Pacific troposphere from a series of 41 flights, which took place in March-April 1999 as part of the NASA Pacific Exploratory Mission (PEM)-Tropics B mission. Ambient CH2O was collected in aqueous media and quantified using an enzyme-derivatization fluorescence technique. Primary calibration was performed using aqueous standards and known flow rates. Occasionally, CH2O gas standard additions to ambient air were performed as a secondary calibration. Analytical blanks were determined by replacing ambient air with pure air. The estimated precision was +/-30 pptv and the estimated accuracy was the sum of +/-30 parts per trillion by volume (pptv) +/-15% of the measured value. Approximately 25% of the observations were less than the instrumental detection limit of 50 pptv, and 85% of these occurred above 6 km. CH2O mixing ratios decreased with altitude; for example, near the equator the median value in the lowest 2 km was 275 pptv, decreased to 150 pptv by 6 kin and was below 100 pptv above 8 km. Between 130 and 170 W and below 1 km, a small variation of CH2O mixing ratio with latitude was noted as near-surface median mixing ratios decreased near the equator (275 pptv) and were greater on either side (375 pptv). A marked decrease in near-surface CH2O (200 pptv) was noted south of 23degreesS on two flights. Between 3degrees and 23degreesS, median CH2O mixing ratios were lower in the eastern tropical Pacific than in the western or central Pacific; nominal differences were >100 pptv near the surface to similar to100 pptv at midaltitude to similar to50 pptv at high attitude. Off the coast of Central America and Mexico, mixing ratios as high as 1200 pptv were observed in plumes that originated to the east over land. CH2O observations were consistently higher than the results from a point model constrained by other photochemical species and meteorological parameters. Regardless of latitude or longitude, agreement was best at altitudes above 4 kin where the difference between measured and modeled CH2O medians was less than 50 pptv. Below 2 km in the model median was approximately 150 pptv less than the measured median.
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页码:32717 / 32731
页数:15
相关论文
共 38 条
[1]   THE TROPOSPHERIC DISTRIBUTION OF FORMALDEHYDE DURING TROPOZ-II [J].
ARLANDER, DW ;
BRUNING, D ;
SCHMIDT, U ;
EHHALT, DH .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 1995, 22 (03) :251-269
[2]   GASEOUS OXYGENATED HYDROCARBONS IN THE REMOTE MARINE TROPOSPHERE [J].
ARLANDER, DW ;
CRONN, DR ;
FARMER, JC ;
MENZIA, FA ;
WESTBERG, HH .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1990, 95 (D10) :16391-16403
[3]   Formaldehyde production in clean marine air [J].
Ayers, GP ;
Gillett, RW ;
Granek, H ;
deServes, C ;
Cox, RA .
GEOPHYSICAL RESEARCH LETTERS, 1997, 24 (04) :401-404
[4]   AQUEOUS-PHASE SOURCE OF FORMIC-ACID IN CLOUDS [J].
CHAMEIDES, WL ;
DAVIS, DD .
NATURE, 1983, 304 (5925) :427-429
[5]   Convective injection and photochemical decay of peroxides in the tropical upper troposphere: Methyl iodide as a tracer of marine convection [J].
Cohan, DS ;
Schultz, MG ;
Jacob, DJ ;
Heikes, BG ;
Blake, DR .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D5) :5717-5724
[6]   Assessment of upper tropospheric HOx sources over the tropical Pacific based on NASA GTE/PEM data:: Net effect on HOx and other photochemical parameters [J].
Crawford, J ;
Davis, D ;
Olson, J ;
Chen, G ;
Liu, S ;
Gregory, G ;
Barrick, J ;
Sachse, G ;
Sandholm, S ;
Heikes, B ;
Singh, H ;
Blake, D .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D13) :16255-16273
[7]  
FINLAYSONPITTS BJ, 1986, ATMOPOSPHERIC CHEM F
[8]   Intercomparison of six ambient [CH2O] measurement techniques [J].
Gilpin, T ;
Apel, E ;
Fried, A ;
Wert, B ;
Calvert, J ;
Zhang, GF ;
Dasgupta, PK ;
Harder, JW ;
Heikes, B ;
Hopkins, B ;
Westberg, H ;
Kleindienst, T ;
Lee, YN ;
Zhou, XL ;
Lonneman, W ;
Sewell, S .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1997, 102 (D17) :21161-21188
[9]   Formaldehyde methods comparison in the remote lower troposphere during the Mauna Loa photochemistry experiment 2 [J].
Heikes, B ;
McCully, B ;
Zhou, X ;
Lee, YN ;
Mopper, K ;
Chen, X ;
Mackay, G ;
Karecki, D ;
Schiff, H ;
Campos, T ;
Atlas, E .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D9) :14741-14755
[10]   Ozone, hydroperoxides, oxides of nitrogen, and hydrocarbon budgets in the marine boundary layer over the South Atlantic [J].
Heikes, B ;
Lee, MH ;
Jacob, D ;
Talbot, R ;
Bradshaw, J ;
Singh, H ;
Blake, D ;
Anderson, B ;
Fuelberg, H ;
Thompson, AM .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1996, 101 (D19) :24221-24234