Mercury in the sediments of freshwater lakes in Ny-Ålesund, Arctic

被引:9
作者
Gopikrishna, V. G. [1 ]
Kannan, V. M. [1 ]
Binish, M. B. [1 ]
Abdul Shukkur, M. [1 ]
Krishnan, K. P. [2 ]
Mohan, Mahesh [1 ]
机构
[1] Mahatma Gandhi Univ, Sch Environm Sci, Kottayam 686560, Kerala, India
[2] Natl Ctr Polar & Ocean Res, Vasco Da Gama 403802, Goa, India
关键词
Pollution; Metal; Svalbard; Methylation; Fractionation; ATMOSPHERIC MERCURY; ACCUMULATION RATES; ELEMENTAL MERCURY; ORGANIC-MATTER; 10-YEAR TRENDS; TRACE-METALS; METHYLMERCURY; TRANSPORT; FRACTIONATION; CONTAMINATION;
D O I
10.1007/s10661-020-08511-y
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
Mercury and its speciation in aquatic ecosystems have been assessed globally. Even though previous studies were limited to Arctic freshwater lakes, they are highly significant in the context of the changing climate. The present study is based on sediment samples collected from three Arctic freshwater lakes over a period of 4 years (2015-2018). The samples were analysed for total mercury (THg), methyl mercury (MHg), and various mercury fractions. The observed mean THg and MHg concentrations were 22.23 ng/g and 0.41 ng/g respectively; these values were comparable with those for other Arctic freshwater lakes. The mercury content significantly varied among the years as well as among the lakes. Changes in snowdrift and meltwater inputs, which are the major sources of water for the lakes, may have influenced the sediment mercury content along with geographical location and increased productivity. The results of MHg indicated the susceptibility of lake sediments to methylation. The major fractions observed were the organo-chelated form of mercury, followed by the elemental and water-soluble forms. These results indicate the availability of mercury for methylation. Hence, it is necessary to conduct more studies on the influence of climate change, mercury release through permafrost melting, and atmospheric deposition.
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页数:10
相关论文
共 58 条
[1]  
[Anonymous], 2004, IMP WARM ARCT, P1
[2]  
Arctic Monitoring and Assessment Programme, 2011, MERC ARCT
[3]   The Arctic: a sink for mercury [J].
Ariya, PA ;
Dastoor, AP ;
Amyot, M ;
Schroeder, WH ;
Barrie, L ;
Anlauf, K ;
Raofie, F ;
Ryzhkov, A ;
Davignon, D ;
Lalonde, J ;
Steffen, A .
TELLUS SERIES B-CHEMICAL AND PHYSICAL METEOROLOGY, 2004, 56 (05) :397-403
[4]   Is there a future for sequential chemical extraction? [J].
Bacon, Jeffrey R. ;
Davidson, Christine M. .
ANALYST, 2008, 133 (01) :25-46
[5]   Global transport of anthropogenic contaminants and the consequences for the Arctic marine ecosystem [J].
Bard, SM .
MARINE POLLUTION BULLETIN, 1999, 38 (05) :356-379
[6]  
Bedowski J, 2015, CHEMOSPHERE, V122, P190, DOI DOI 10.1016/J.CHEMOSPHERE.2014.11.050
[7]   Ten-year trends in atmospheric mercury concentrations, meteorological effects and climate variables at Zeppelin, Ny-Alesund [J].
Berg, T. ;
Pfaffhuber, K. A. ;
Cole, A. S. ;
Engelsen, O. ;
Steffen, A. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2013, 13 (13) :6575-6586
[8]   Selective extractions to assess the biogeochemically relevant fractionation of inorganic mercury in sediments and soils [J].
Bloom, NS ;
Preus, E ;
Katon, J ;
Hiltner, M .
ANALYTICA CHIMICA ACTA, 2003, 479 (02) :233-248
[9]   Potential atmospheric transport pathways for mercury measured in the Canadian high arctic [J].
Cheng, MD ;
Schroeder, WH .
JOURNAL OF ATMOSPHERIC CHEMISTRY, 2000, 35 (01) :101-107
[10]   Ten-year trends of atmospheric mercury in the high Arctic compared to Canadian sub-Arctic and mid-latitude sites [J].
Cole, A. S. ;
Steffen, A. ;
Pfaffhuber, K. A. ;
Berg, T. ;
Pilote, M. ;
Poissant, L. ;
Tordon, R. ;
Hung, H. .
ATMOSPHERIC CHEMISTRY AND PHYSICS, 2013, 13 (03) :1535-1545