DISTRIBUTION OF METHYLCHLORIDE, DICHLOROMETHANE, TRICHLOROETHENE AND TETRACHLOROETHENE OVER THE NORTH AND SOUTH-ATLANTIC

被引:71
作者
KOPPMANN, R
JOHNEN, FJ
PLASSDULMER, C
RUDOLPH, J
机构
关键词
D O I
10.1029/93JD01864
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
During the cruise ANT VIII/1 of the German R/V Polarstern in August/September 1989 the latitudinal distributions of the atmospheric concentrations of methylchloride, dichloromethane, trichloroethene, and tetrachloroethene were measured over the Atlantic between 45-degrees-N and 30-degrees-S by in situ gas chromatography. With the exception of trichloroethene they showed mixing ratios well above the lower limit of detection. The methylchloride distribution was uniform with average mixing ratios of 532 +/- 8 and 550 +/- 12 ppt in the northern and southern Hemispheres, respectively. Dichloromethane increased linearly between the Intertropical Convergence Zone and 45-degrees-N with average mixing ratios of 36 +/- 6 ppt and was almost constant in the southern hemisphere with an average of 18 +/- 1 ppt. Tetrachloroethene mixing ratios were between less than 1 and 10 ppt in the northern hemisphere and always below 3 ppt in the southern hemisphere. Similar to dichloromethane, tetrachloroethene was nearly constant in the southern hemisphere and increased linearly toward northern latitudes. This is compatible with the predominantly industrial origin of these compounds. Trichloroethene varied between 0.3 ppt and about 15 ppt in the northern hemisphere with an average of 3 +/- 1 ppt and was generally lower than 1 ppt in the southern hemisphere with mixing ratios often near or below the detection limit of 0.1 ppt. For CH3Cl we estimate a global turnover of 3.5 x 10(12) g/yr which is compatible with previous results. Using a simple model calculation our measurements imply a global turnover for CH2Cl2 and C2Cl4 of 0.9 X 10(12) g/yr and 0.6 x 10(12) g/yr, respectively.
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页码:20517 / 20526
页数:10
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共 35 条
  • [1] [Anonymous], 1986, AIR POLLUTION, DOI DOI 10.1007/978-3-540-39222-4_2
  • [2] EVALUATED KINETIC AND PHOTOCHEMICAL DATA FOR ATMOSPHERIC CHEMISTRY .3. IUPAC SUBCOMMITTEE ON GAS KINETIC DATA EVALUATION FOR ATMOSPHERIC CHEMISTRY
    ATKINSON, R
    BAULCH, DL
    COX, RA
    HAMPSON, RF
    KERR, JA
    TROE, J
    [J]. JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1989, 18 (02) : 881 - 1097
  • [3] CHEMISTRY OF ORGANIC TRACES IN AIR .6. DISTRIBUTION OF CHLORINATED-C1 CHLORINATED-C4 HYDROCARBONS IN AIR OVER THE NORTHERN AND SOUTHERN ATLANTIC-OCEAN
    CLASS, T
    BALLSCHMITER, K
    [J]. CHEMOSPHERE, 1986, 15 (04) : 413 - 427
  • [4] PRODUCTION OF VOLATILE METABOLITES BY SPECIES OF FOMES
    COWAN, MI
    GLEN, AT
    HUTCHINSON, SA
    MACCARTNEY, ME
    MACKINTOSH, JM
    MOSS, AM
    [J]. TRANSACTIONS OF THE BRITISH MYCOLOGICAL SOCIETY, 1973, 60 (APR): : 347 - 351
  • [5] PHOTOCHEMICAL OXIDATION OF HALOCARBONS IN TROPOSPHERE
    COX, RA
    DERWENT, RG
    EGGLETON, AEJ
    LOVELOCK, JE
    [J]. ATMOSPHERIC ENVIRONMENT, 1976, 10 (04) : 305 - 308
  • [6] HALOGENATED COMPOUND IDENTIFICATION AND MEASUREMENT IN TROPOSPHERE AND LOWER STRATOSPHERE
    CRONN, DR
    RASMUSSEN, RA
    ROBINSON, E
    HARSCH, DE
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-OCEANS AND ATMOSPHERES, 1977, 82 (37): : 5935 - 5944
  • [7] BIOMASS BURNING AS A SOURCE OF ATMOSPHERIC GASES CO, H-2, N2O, NO, CH3CL AND COS
    CRUTZEN, PJ
    HEIDT, LE
    KRASNEC, JP
    POLLOCK, WH
    SEILER, W
    [J]. NATURE, 1979, 282 (5736) : 253 - 256
  • [8] EHHALT DH, 1984, JUL1942 KERN FORSCH, P1
  • [9] Finlayson-Pitts B.J., 1986, ATMOSPHERIC CHEM FUN
  • [10] METHANE, CARBON-MONOXIDE AND METHYLCHLOROFORM IN THE SOUTHERN-HEMISPHERE
    FRASER, PJ
    HYSON, P
    RASMUSSEN, RA
    CRAWFORD, AJ
    KHALIL, MAK
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1986, 4 (01) : 3 - 42