Observation of filterable bromine variabilities during Arctic tropospheric ozone depletion events in high (1hour) time resolution

被引:27
|
作者
Langendörfer, U [1 ]
Lehrer, E [1 ]
Wagenbach, D [1 ]
Platt, U [1 ]
机构
[1] Univ Heidelberg, Inst Umweltphys, D-69120 Heidelberg, Germany
关键词
tropospheric ozone; atmospheric aerosol particles; halogen chemistry; Arctic regions;
D O I
10.1023/A:1006217001008
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The halogen ions Br and Cl- together with NO3-, SO4(=), MSA(-) (methane sulfonate), Na+ and NH4+ were analysed by ion chromatography in extracts of more than 800 aerosol cellulose filter samples taken at Ny (A) over circle lesund, Svarbard (79 degrees N, 12 degrees E) in spring 1996 (March 27 - May 16) within the European Union project ARCTOC (Arctic Tropospheric Ozone Chemistry). Anticorrelated variations between f-Br (filterable bromine, i.e. water soluble bromine species that can be collected by aerosol filters) and ozone within the arctic troposphere were evaluated at a resolution of 1 or 2 hours for periods with depleted ozone and 4 hours at normal ozone. A mean f-Br concentration of 11 ng m(-3) (0.14 nmol m(-3)) was observed for the whole campaign, while maximum concentrations of 80 ng m(-3) (1 nmol m(-3)) were detected during two total O-3-depletion events (O-3 drop to mixing ratios below the detection limit of < 2 ppb). Anticorrelation between f-Br and O-3 was also seen during minor O-3-depletion episodes (sudden drop in O-3 by at feast 10 ppb, but O-3 Still exceeding the detection limit) and even for ozone variations near its background level (40-50 ppb). A time lag of about 10 hours between the change of ozone and of f-Br concentrations could only be found during a total ozone depletion event, when f-Br reached its maximum values several hours after ozone was totally destroyed. Bromine oxide (BrO) concentrations, measured by DOAS (Differential Optical Absorption Spectroscopy), and f-Br showed a coincident variability during almost the entire campaign (except in the case of total O-3-loss). Frequently enhanced anthropogenic nitrate and sulphate concentrations were observed during O-3-depletion periods. At O-3 concentrations < 10 ppb sulphate and nitrate exceed their typical mean level by 54% and 77%, respectively. This may indicate a possible connection between acidity and halogen release.
引用
收藏
页码:39 / 54
页数:16
相关论文
共 8 条
  • [1] Observation of Filterable Bromine Variabilities During Arctic Tropospheric Ozone Depletion Events in High (1hour) Time Resolution
    U. Langendörfer
    E. Lehrer
    D. Wagenbach
    U. Platt
    Journal of Atmospheric Chemistry, 1999, 34 : 39 - 54
  • [2] Influence of the Background Nitrogen Oxides on the Tropospheric Ozone Depletion Events in the Arctic during Springtime
    Zhou, Jiashu
    Cao, Le
    Li, Simeng
    ATMOSPHERE, 2020, 11 (04)
  • [3] Bromine atom production and chain propagation during springtime Arctic ozone depletion events in Barrow, Alaska
    Thompson, Chelsea R.
    Shepson, Paul B.
    Liao, Jin
    Huey, L. Greg
    Cantrell, Chris
    Flocke, Frank
    Orlando, John
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2017, 17 (05) : 3401 - 3421
  • [4] Short-term variations in the 13C/12C ratio of CO as a measure of Cl activation during tropospheric ozone depletion events in the Arctic
    Röckmann, T
    Brenninkmeijer, CAM
    Crutzen, PJ
    Platt, U
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D1) : 1691 - 1697
  • [5] A three-dimensional simulation and process analysis of tropospheric ozone depletion events (ODEs) during the springtime in the Arctic using CMAQ (Community Multiscale Air Quality Modeling System)
    Cao, Le
    Li, Simeng
    Gu, Yicheng
    Luo, Yuhan
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2023, 23 (05) : 3363 - 3382
  • [6] Coupled evolution of BrOx-ClOx-HOx-NOx chemistry during bromine-catalyzed ozone depletion events in the arctic boundary layer -: art. no. 8368
    Evans, MJ
    Jacob, DJ
    Atlas, E
    Cantrell, CA
    Eisele, F
    Flocke, F
    Fried, A
    Mauldin, RL
    Ridley, BA
    Wert, B
    Talbot, R
    Blake, D
    Heikes, B
    Snow, J
    Walega, J
    Weinheimer, AJ
    Dibb, J
    JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 2003, 108 (D4)
  • [7] Photochemical production and loss of organic acids in high Arctic aerosols during long-range transport and polar sunrise ozone depletion events
    Kawamura, K
    Imai, Y
    Barrie, LA
    ATMOSPHERIC ENVIRONMENT, 2005, 39 (04) : 599 - 614
  • [8] Time-dependent 3D simulations of tropospheric ozone depletion events in the Arctic spring using the Weather Research and Forecasting model coupled with Chemistry (WRF-Chem)
    Herrmann, Maximilian
    Sihler, Holger
    Friess, Udo
    Wagner, Thomas
    Platt, Ulrich
    Gutheil, Eva
    ATMOSPHERIC CHEMISTRY AND PHYSICS, 2021, 21 (10) : 7611 - 7638