Airborne observations of dust aerosol over the North Atlantic Ocean during ACE 2:: Indications for heterogeneous ozone destruction

被引:112
作者
de Reus, M
Dentener, F
Thomas, A
Borrmann, S
Ström, J
Lelieveld, J
机构
[1] Inst Marine & Atmospher Res Utrecht, NL-3584 CC Utrecht, Netherlands
[2] Johannes Gutenberg Univ Mainz, Inst Atmospher Phys, D-55099 Mainz, Germany
[3] Stockholm Univ, Inst Appl Environm Res, Air Pollut Lab, S-10691 Stockholm, Sweden
[4] Forschungszentrum Julich, Inst Stratospher Chem, D-52425 Julich, Germany
关键词
D O I
10.1029/2000JD900164
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Aerosol size distribution measurements have been performed in the free troposphere during the Second Aerosol Characterization Experiment (ACE 2) near Tenerife, Canary Islands, in July 1997. During one measurement flight, on July 8, a uniform aerosol layer was encountered between 2.5 and 5.5 km altitude, characterized by a relatively low Aitken mode particle number concentration and high concentrations of accumulation and coarse mode particles? resulting in a relatively large aerosol surface area and mass, which is estimated to be about 400 mu g m(-3). Five-day backward trajectories indicate that the aerosol in this layer was mineral dust originating from arid regions on the North African continent. The dust layer was associated with reduced ozone mixing ratios. Model simulations have been performed with a photochemical box model including different heterogeneous removal reactions to study the interaction between gas phase chemistry and mineral aerosol. The best agreement between the observed and modeled ozone concentrations was obtained when heterogeneous removal of ozone and precursor gases on dust aerosol were taken into account. Heterogeneous O-3 loss is estimated at 4 ppbv O-3 per day. Although uncertainties concerning heterogeneous ozone removal remain, in particular related to the reactive uptake coefficient of O-3, it is likely that the loss of O-3 and precursor gases on mineral dust aerosol significantly reduces the O-3 abundance in large-scale dust plumes.
引用
收藏
页码:15263 / 15275
页数:13
相关论文
共 54 条
  • [1] Heterogeneous interactions of HOBr, HNO3, O3, and NO2 with deliquescent NaCl aerosols at room temperature
    Abbatt, JPD
    Waschewsky, GCG
    [J]. JOURNAL OF PHYSICAL CHEMISTRY A, 1998, 102 (21) : 3719 - 3725
  • [2] Andreae M.O., 1995, World Survey of Climatology, vol. 16, V16, P341, DOI 10.1016/S0168-6321(06)80033-7
  • [3] [Anonymous], 1996, Intergovernmental Panel on Climate Change
  • [4] VOLUME AND MASS OF YELLOW SAND DUST IN THE AIR OVER JAPAN AS ESTIMATED FROM ATMOSPHERIC TURBIDITY
    ARAO, K
    ISHIZAKA, Y
    [J]. JOURNAL OF THE METEOROLOGICAL SOCIETY OF JAPAN, 1986, 64 (01) : 79 - 94
  • [5] INTERPRETATION OF MEASUREMENTS MADE BY THE FORWARD SCATTERING SPECTROMETER PROBE (FSSP-300) DURING THE AIRBORNE ARCTIC STRATOSPHERIC EXPEDITION
    BAUMGARDNER, D
    DYE, JE
    GANDRUD, BW
    KNOLLENBERG, RG
    [J]. JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D8) : 8035 - 8046
  • [6] In situ trace gas and particle measurements in the summer lower stratosphere during STREAM II: Implications for O-3 production
    Bregman, A
    Arnold, F
    Burger, V
    Fischer, H
    Lelieveld, J
    Scheeren, BA
    Schneider, J
    Siegmund, PC
    Strom, J
    Waibel, A
    Wauben, WMF
    [J]. JOURNAL OF ATMOSPHERIC CHEMISTRY, 1997, 26 (03) : 275 - 310
  • [7] CLIMATE FORCING BY ANTHROPOGENIC AEROSOLS
    CHARLSON, RJ
    SCHWARTZ, SE
    HALES, JM
    CESS, RD
    COAKLEY, JA
    HANSEN, JE
    HOFMANN, DJ
    [J]. SCIENCE, 1992, 255 (5043) : 423 - 430
  • [8] CLAQUIN T, 1988, TELLUS, V50, P491
  • [9] CRUTZEN PJ, 1994, ENV OXIDANTS, P63
  • [10] CURTIS AE, 1987, 12805 AERE R HARW LA