Global lifetime of elemental mercury against oxidation by atomic bromine in the free troposphere
نویسندگان
چکیده
[1] We calculate the global mean atmospheric lifetime of elemental mercury (Hg) against oxidation by atomic bromine (Br) in the troposphere by combining recent kinetic data for the Hg-Br system with modeled global concentrations of tropospheric Br. We obtain a lifetime of 0.5–1.7 years based on the range of kinetic data, implying that oxidation of Hg by Br is a major, and possibly dominant, global sink for Hg. Most of the oxidation takes place in the middle and upper troposphere, where Br concentrations are high and where cold temperatures suppress thermal decomposition of the HgBr intermediate. This oxidation mechanism is consistent with mercury observations, including in particular high gaseous Hg(II) concentrations in Antarctic summer. Better freetropospheric measurements of bromine radicals and further kinetic study of the Hg-Br system are essential to more accurately assess the global importance of Br as an oxidant of atmospheric Hg. Citation: Holmes, C. D., D. J. Jacob, and X. Yang (2006), Global lifetime of elemental mercury against oxidation by atomic bromine in the free troposphere, Geophys. Res. Lett., 33, L20808, doi:10.1029/2006GL027176.
منابع مشابه
Modeling the observed tropospheric BrO background: Importance of multiphase chemistry and implications for ozone, OH, and mercury
Aircraft and satellite observations indicate the presence of ppt (ppt ≡ pmol/mol) levels of BrO in the free troposphere with important implications for the tropospheric budgets of ozone, OH, and mercury. We can reproduce these observations with the GEOS-Chem global tropospheric chemistry model by including a broader consideration of multiphase halogen (Br-Cl) chemistry than has been done in the...
متن کاملA new mechanism for atmospheric mercury redox chemistry: implications for the global mercury budget
Mercury (Hg) is emitted to the atmosphere mainly as volatile elemental Hg0. Oxidation to water-soluble HgII plays a major role in Hg deposition to ecosystems. Here, we implement a new mechanism for atmospheric Hg0 /HgII redox chemistry in the GEOS-Chem global model and examine the implications for the global atmospheric Hg budget and deposition patterns. Our simulation includes a new coupling o...
متن کاملTropospheric bromine chemistry: implications for present and pre-industrial ozone and mercury
We present a new model for the global tropospheric chemistry of inorganic bromine (Bry) coupled to oxidant-aerosol chemistry in the GEOS-Chem chemical transport model (CTM). Sources of tropospheric Bry include debromination of sea-salt aerosol, photolysis and oxidation of short-lived bromocarbons, and transport from the stratosphere. Comparison to a GOME-2 satellite climatology of tropospheric ...
متن کاملSubtropical subsidence and surface deposition of oxidized mercury produced in the free troposphere
Oxidized mercury (Hg(II)) is chemically produced in the atmosphere by oxidation of elemental mercury and is directly emitted by anthropogenic activities. We use the GEOS-Chem global chemical transport model with gaseous oxidation driven by Br atoms, to quantify how surface deposition of Hg(II) is influenced by Hg(II) production at different atmospheric heights. We tag Hg(II) 10 chemically produ...
متن کاملActive and widespread halogen chemistry in the tropical and subtropical free troposphere.
Halogens in the troposphere are increasingly recognized as playing an important role for atmospheric chemistry, and possibly climate. Bromine and iodine react catalytically to destroy ozone (O3), oxidize mercury, and modify oxidative capacity that is relevant for the lifetime of greenhouse gases. Most of the tropospheric O3 and methane (CH4) loss occurs at tropical latitudes. Here we report sim...
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
عنوان ژورنال:
دوره شماره
صفحات -
تاریخ انتشار 2006