The Arctic: a sink for mercury

被引:183
作者
Ariya, PA
Dastoor, AP
Amyot, M
Schroeder, WH
Barrie, L
Anlauf, K
Raofie, F
Ryzhkov, A
Davignon, D
Lalonde, J
Steffen, A
机构
[1] McGill Univ, Dept Atmospher Sci, Montreal, PQ H3A 2K6, Canada
[2] McGill Univ, Dept Ocean Sci, Montreal, PQ H3A 2K6, Canada
[3] Environm Canada, Meteorol Serv Canada, Dorval, PQ M3H 5T4, Canada
[4] Univ Montreal, Dept Biol Sci, Montreal, PQ H2V 2S9, Canada
[5] World Meteorol Org, AREP, Endironm Div, CH-1211 Geneva 2, Switzerland
来源
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY | 2004年 / 56卷 / 05期
关键词
D O I
10.1111/j.1600-0889.2004.00118.x
中图分类号
P4 [大气科学(气象学)];
学科分类号
0706 ; 070601 ;
摘要
Mercury is a persistent, toxic and bio-accumulative pollutant of global interest. Its main mass in the troposphere is in the form of elemental gas-phase mercury. Rapid, near-complete depletion of mercury has been observed during spring in the atmospheric boundary layer of frozen marine areas in Arctic, sub-Arctic and Antarctic locations. It is strongly correlated with ozone depletion. To date, evidence has indicated strongly that chemistry involving halogen gases from surface sea-salt is the mechanism of this destruction. Precisely which halogen gases are the main players has remained unresolved. Our novel kinetic data and multiscale modelling show that Br atoms and BrO radicals are the most effective halogens driving mercury oxidation. The reduction of oxidized mercury deposited in the snow pack back to Hg-0 and subsequent diffusion to the atmosphere is observed. However, it cannot compensate for the total deposition, and a net accumulation occurs. We use a unique global atmospheric mercury model to estimate that halogen-driven mercury depletion events result in a 44% increase in the net deposition of mercury to the Arctic. Over a 1-yr cycle, we estimate an accumulation of 325 tons of mercury in the Arctic.
引用
收藏
页码:397 / 403
页数:7
相关论文
共 35 条
[1]  
Agency for Toxic Substances and Disease Registry, 1999, TOXFAQS MERC
[2]   Behavior of mercury in snow from different latitudes [J].
Amyot, M ;
Lalonde, JD ;
Ariya, PA ;
Dastoor, A .
JOURNAL DE PHYSIQUE IV, 2003, 107 :45-48
[3]  
Arctic Monitoring and Assessment Programme (AMAP), 1998, ARCT POLL ISS STAT A
[4]   Trichloroethene and tetrachloroethene: Tropospheric probes for Cl- and Br-atom reactions during polar sunrise [J].
Ariya, PA ;
Catoire, V ;
Sander, R ;
Niki, H ;
Harris, GW .
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 1997, 49 (05) :583-591
[5]   Reactions of gaseous mercury with atomic and molecular halogens: Kinetics, product studies, and atmospheric implications [J].
Ariya, PA ;
Khalizov, A ;
Gidas, A .
JOURNAL OF PHYSICAL CHEMISTRY A, 2002, 106 (32) :7310-7320
[6]   Atmospheric transoformation of elemental mercury upon reactions with halogens [J].
Ariya, PA ;
Ryzhkov, A .
JOURNAL DE PHYSIQUE IV, 2003, 107 :57-59
[7]   Arctic tropospheric chemistry: an overview [J].
Barrie, L ;
Platt, U .
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 1997, 49 (05) :450-454
[8]   OZONE DESTRUCTION AND PHOTOCHEMICAL-REACTIONS AT POLAR SUNRISE IN THE LOWER ARCTIC ATMOSPHERE [J].
BARRIE, LA ;
BOTTENHEIM, JW ;
SCHNELL, RC ;
CRUTZEN, PJ ;
RASMUSSEN, RA .
NATURE, 1988, 334 (6178) :138-141
[9]   A modeling study of the mechanism of the halogen-ozone-mercury homogeneous reactions in the troposphere during the polar spring [J].
Calvert, JG ;
Lindberg, SE .
ATMOSPHERIC ENVIRONMENT, 2003, 37 (32) :4467-4481
[10]   Global circulation of atmospheric mercury: a modelling study [J].
Dastoor, AP ;
Larocque, Y .
ATMOSPHERIC ENVIRONMENT, 2004, 38 (01) :147-161