Oceanic distributions and emissions of short-lived halocarbons

被引:137
作者
Butler, James H.
King, Daniel B.
Lobert, Juergen M.
Montzka, Stephen A.
Yvon-Lewis, Shari A.
Hall, Bradley D.
Warwick, Nicola J.
Mondeel, Debra J.
Aydin, Murat
Elkins, James W.
机构
[1] NOAA, Earth Syst Res Lab, Global Monitoring Div, Boulder, CO 80305 USA
[2] Univ Colorado, Cooperat Inst Res Environm Sci, Boulder, CO 80309 USA
[3] Univ Cambridge, Dept Chem, Ctr Atmospher Sci, Cambridge CB2 1TN, England
[4] Univ Calif Irvine, Dept Earth Syst Sci, Irvine, CA 92697 USA
基金
英国自然环境研究理事会;
关键词
D O I
10.1029/2006GB002732
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
[1] Using data from seven cruises over a 10-year span, we report marine boundary layer mixing ratios (i.e., dry mole fractions as pmol mol(-1) or ppt), degrees of surface seawater saturation, and air-sea fluxes of three short-lived halocarbons that are significant in tropospheric and potentially stratospheric chemistry. CHBr3, CH2Br2, and CH3I were all highly supersaturated almost everywhere, all the time. Highest saturations of the two polybrominated gases were observed in coastal waters and areas of upwelling, such as those near the equator and along ocean fronts. CH3I distributions reflected the different chemistry and cycling of this gas in both the water and the atmosphere. Seasonal variations in fluxes were apparent where cruises overlapped and were consistent among oceans. Undersaturations of these gases were noted at some locations in the Southern Ocean, owing to mixing of surface and subsurface waters, not necessarily biological or chemical sinks. The Pacific Ocean appears to be a much stronger source of CHBr3 to the marine boundary layer than the Atlantic. The high supersaturations, fluxes, and marine boundary layer mixing ratios in the tropics are consistent with the suggestion that tropical convection could deliver some portion of these gases and their breakdown products to the upper troposphere and lower stratosphere.
引用
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页数:11
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[31]   Oceanic bromoform sources for the tropical atmosphere [J].
Quack, B ;
Atlas, E ;
Petrick, G ;
Stroud, V ;
Schauffler, S ;
Wallace, DWR .
GEOPHYSICAL RESEARCH LETTERS, 2004, 31 (23) :1-4
[32]   Air-sea flux of bromoform: Controls, rates, and implications [J].
Quack, B ;
Wallace, DWR .
GLOBAL BIOGEOCHEMICAL CYCLES, 2003, 17 (01) :23-1
[33]   PHOTOSYNTHESIS AND FISH PRODUCTION IN SEA [J].
RYTHER, JH .
SCIENCE, 1969, 166 (3901) :72-+
[34]   Atmospheric chemistry - Biogenic bromine [J].
Salawitch, RJ .
NATURE, 2006, 439 (7074) :275-277
[35]  
SANDER SP, 2002, JPL PUBL, V225
[36]   GC DETERMINATION OF VOLATILE ORGANOIODINE AND ORGANOBROMINE COMPOUNDS IN ARCTIC SEAWATER AND AIR SAMPLES [J].
SCHALL, C ;
HEUMANN, KG .
FRESENIUS JOURNAL OF ANALYTICAL CHEMISTRY, 1993, 346 (6-9) :717-722
[37]   Halocarbon and dimethyl sulphide studies around the Mascarene Plateau [J].
Smythe-Wright, D ;
Boswell, SM ;
Lucas, CH ;
New, AL ;
Varney, MS .
PHILOSOPHICAL TRANSACTIONS OF THE ROYAL SOCIETY A-MATHEMATICAL PHYSICAL AND ENGINEERING SCIENCES, 2005, 363 (1826) :169-185
[38]   On the distribution and variability of ozone in the tropical upper troposphere: Implications for tropical deep convection and chemical-dynamical coupling [J].
Solomon, S ;
Thompson, DWJ ;
Portmann, RW ;
Oltmans, SJ ;
Thompson, AM .
GEOPHYSICAL RESEARCH LETTERS, 2005, 32 (23) :1-4
[39]   ON THE ROLE OF IODINE IN OZONE DEPLETION [J].
SOLOMON, S ;
GARCIA, RR ;
RAVISHANKARA, AR .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1994, 99 (D10) :20491-20499
[40]   ON THE EVALUATION OF OZONE DEPLETION POTENTIALS [J].
SOLOMON, S ;
MILLS, M ;
HEIDT, LE ;
POLLOCK, WH ;
TUCK, AF .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1992, 97 (D1) :825-842