Global 3-D land-ocean-atmosphere model for mercury:: Present-day versus preindustrial cycles and anthropogenic enrichment factors for deposition

被引:246
作者
Selin, Noelle E. [2 ,3 ]
Jacob, Daniel J. [2 ,3 ]
Yantosca, Robert M. [2 ,3 ]
Strode, Sarah [4 ]
Jaegle, Lyatt [4 ]
Sunderland, Elsie M. [1 ]
机构
[1] US EPA, Washington, DC 20460 USA
[2] Harvard Univ, Sch Engn & Appl Sci, Cambridge, MA 02138 USA
[3] Harvard Univ, Dept Earth & Planetary Sci, Cambridge, MA 02138 USA
[4] Univ Washington, Dept Atmospher Sci, Seattle, WA 98195 USA
关键词
D O I
10.1029/2007GB003040
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
We develop a mechanistic representation of land-atmosphere cycling in a global 3-D ocean-atmosphere model of mercury (GEOS-Chem). The resulting land-oceanatmosphere model is used to construct preindustrial and present biogeochemical cycles of mercury, to examine the legacy of past anthropogenic emissions, to map anthropogenic enrichment factors for deposition, and to attribute mercury deposition in the United States. Land emission in the model includes prompt recycling of recently deposited mercury (600 Mg a(-1) for present day), soil volatilization (550 Mg a(-1)), and evapotranspiration (550 Mg a(-1)). The spatial distribution of soil concentrations is derived from local steady state between land emission and deposition in the preindustrial simulation, augmented for the present day by a 15% increase in the soil reservoir distributed following the pattern of anthropogenic deposition. Mercury deposition and hence emission are predicted to be highest in the subtropics. Our atmospheric lifetime of mercury against deposition (0.50 year) is shorter than past estimates because of our accounting of Hg(0) dry deposition, but recycling from surface reservoirs results in an effective lifetime of 1.6 years against transfer to long-lived reservoirs in the soil and deep ocean. Present-day anthropogenic enrichment of mercury deposition exceeds a factor of 5 in continental source regions. We estimate that 68% of the deposition over the United States is anthropogenic, including 20% from North American emissions (20% primary and <1% recycled through surface reservoirs), 31% from emissions outside North America (22% primary and 9% recycled), and 16% from the legacy of anthropogenic mercury accumulated in soils and the deep ocean.
引用
收藏
页数:13
相关论文
共 93 条
[91]   A regional scale modeling study of atmospheric transport and transformation of mercury. II. Simulation results for the northeast United States [J].
Xu, XH ;
Yang, XS ;
Miller, DR ;
Helble, JJ ;
Carley, RJ .
ATMOSPHERIC ENVIRONMENT, 2000, 34 (28) :4945-4955
[92]   Mercury air/surface exchange kinetics of background soils of the Tahquamenon River watershed in the Michigan Upper Peninsula [J].
Zhang, H ;
Lindberg, SE ;
Marsik, FJ ;
Keeler, GJ .
WATER AIR AND SOIL POLLUTION, 2001, 126 (1-2) :151-169
[93]   Processes influencing the emission of mercury from soils: A conceptual model [J].
Zhang, H ;
Lindberg, SE .
JOURNAL OF GEOPHYSICAL RESEARCH-ATMOSPHERES, 1999, 104 (D17) :21889-21896