Gaseous (DMS, MSA, SO2, H2SO4 and DMSO) and particulate (sulfate and methanesulfonate) sulfur species over the northeastern coast of Crete

被引:74
作者
Bardouki, H
Berresheim, H
Vrekoussis, M
Sciare, J
Kouvarakis, G
Oikonomou, K
Schneider, J
Mihalopoulos, N
机构
[1] Univ Crete, Dept Chem, ECPL, Iraklion 71409, Greece
[2] DWD, Meteorol Observ, Hohenpeissenberg, Germany
[3] Max Planck Inst Chem, Biogeochem Div, D-55128 Mainz, Germany
关键词
D O I
10.5194/acp-3-1871-2003
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
A detailed study of the levels, the temporal and diurnal variability of the main compounds involved in the biogenic sulfur cycle was carried out in Crete ( Eastern Mediterranean) during the Mediterranean Intensive Oxidant Study (MINOS) field experiment in July-August 2001. Intensive measurements of gaseous dimethylsulfide (DMS), dimethylsulfoxide (DMSO), sulfur dioxide (SO2), sulfuric (H2SO4) and methanesulfonic acids (MSA) and particulate sulfate (SO42-) and methanesulfonate (MS-) have been performed during the campaign. Dimethylsulfide (DMS) levels ranged from 2.9 to 136 pmol.mol(-1) (mean value of 21.7 pmol.mol(-1)) and showed a clear diurnal variation with daytime maximum. During nighttime DMS levels fall close or below the detection limit of 2 pmol.mol(-1). Concurrent measurements of OH and NO3 radicals during the campaign indicate that NO3 levels can explain most of the observed diurnal variation of DMS. Dimethylsulfoxide (DMSO) ranged between 0.02 and 10.1 pmol.mol(-1) (mean value of 1.7 pmol.mol(-1)) and presents a diurnal variation similar to that of DMS. SO2 levels ranged from 220 to 2970 pmol.mol(-1) (mean value of 1030 pmol.mol(-1)), while nss-SO42- and MS- ranged from 330 to 7100 pmol.mol(-1), (mean value of 1440 pmol.mol(-1)) and 1.1 to 37.5 pmol.mol(-1) (mean value of 11.5 pmol.mol(-1)) respectively. Of particular interest are the measurements of gaseous MSA and H2SO4. MSA ranged from below the detection limit (3 x 10(4)) to 3.7 x 10(7) molecules cm(-3), whereas H2SO4 ranged between 1 x 10(5) and 9.0 x 10(7) molecules cm(-3). The measured H2SO4 maxima are among the highest reported in literature and can be attributed to high insolation, absence of precipitation and increased SO2 levels in the area. From the concurrent SO2, OH, and H2SO4 measurements a sticking coefficient of 0.52+/-0.28 was calculated for H2SO4. From the concurrent MSA, OH, and DMS measurements the yield of gaseous MSA from the OH-initiated oxidation of DMS was calculated to range between 0.1-0.4%. This low MSA yield implies that gaseous MSA levels can not account for the observed MS- levels. Heterogeneous reactions of DMSO on aerosols should be considered to explain the observed levels of MS-.
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页码:1871 / 1886
页数:16
相关论文
共 60 条
[11]   Measurements of dimethyl sulfide, dimethyl sulfoxide, dimethyl sulfone, and aerosol ions at Palmer Station, Antarctica [J].
Berresheim, H ;
Huey, JW ;
Thorn, RP ;
Eisele, FL ;
Tanner, DJ ;
Jefferson, A .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D1) :1629-1637
[12]   Sulfur Chemistry in the Antarctic Troposphere Experiment: An overview of project SCATE [J].
Berresheim, H ;
Eisele, FL .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D1) :1619-1627
[13]  
Berresheim H., 1995, COMPOSITION CHEM CLI, P251
[14]   OCEANIC PHYTOPLANKTON, ATMOSPHERIC SULFUR, CLOUD ALBEDO AND CLIMATE [J].
CHARLSON, RJ ;
LOVELOCK, JE ;
ANDREAE, MO ;
WARREN, SG .
NATURE, 1987, 326 (6114) :655-661
[15]   IMPROVED AQUEOUS SCRUBBER FOR COLLECTION OF SOLUBLE ATMOSPHERIC TRACE GASES [J].
COFER, WR ;
COLLINS, VG ;
TALBOT, RW .
ENVIRONMENTAL SCIENCE & TECHNOLOGY, 1985, 19 (06) :557-560
[16]   Dimethyl sulfide oxidation in the equatorial Pacific:: Comparison of model simulations with field observations for DMS, SO2, H2SO4(g), MSA(g), MS, and NSS [J].
Davis, D ;
Chen, G ;
Bandy, A ;
Thornton, D ;
Eisele, F ;
Mauldin, L ;
Tanner, D ;
Lenschow, D ;
Fuelberg, H ;
Huebert, B ;
Heath, J ;
Clarke, A ;
Blake, D .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D5) :5765-5784
[17]   DMS oxidation in the Antarctic marine boundary layer:: Comparison of model simulations and field observations of DMS, DMSO, DMSO2, H2SO4(g), MSA(g), and MSA(p) [J].
Davis, D ;
Chen, G ;
Kasibhatla, P ;
Jefferson, A ;
Tanner, D ;
Eisele, F ;
Lenschow, D ;
Neff, W ;
Berresheim, H .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1998, 103 (D1) :1657-1678
[18]   UPTAKE OF GAS-PHASE SULFUR SPECIES METHANESULFONIC-ACID, DIMETHYLSULFOXIDE, AND DIMETHYL SULFONE BY AQUEOUS SURFACES [J].
DEBRUYN, WJ ;
SHORTER, JA ;
DAVIDOVITS, P ;
WORSNOP, DR ;
ZAHNISER, MS ;
KOLB, CE .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D8) :16927-16932
[19]  
DeMore W.B., 1997, JPL PUBL, P97
[20]   MEASUREMENT OF THE GAS-PHASE CONCENTRATION OF H2SO4 AND METHANE SULFONIC-ACID AND ESTIMATES OF H2SO4 PRODUCTION AND LOSS IN THE ATMOSPHERE [J].
EISELE, FL ;
TANNER, DJ .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1993, 98 (D5) :9001-9010