Species-specific isotope tracers to study the accumulation and biotransformation of mixtures of inorganic and methyl mercury by the microalga Chlamydomonas reinhardtii

被引:28
作者
Bravo, Andrea Garcia [1 ]
Le Faucheur, Severine [1 ]
Monperrus, Mathilde [2 ]
Amouroux, David [2 ]
Slaveykova, Vera I. [1 ]
机构
[1] Univ Geneva, Inst FA Forel, CH-1290 Versoix, Switzerland
[2] Univ Pau & Pays Adour, Lab Chim Analyt Bioinorgan & Environm, Inst Sci Analyt & Physicochim Environm & Mat, IPREM UMR CNRS 5254, F-64053 Pau, France
基金
瑞士国家科学基金会;
关键词
Mercury; Methylmercury; Algae; Uptake; Species-specific isotope tracers; DILUTION ANALYSIS; WATER; METHYLMERCURY; SPECIATION; RESERVOIR; SEDIMENT; COASTAL; LAKE; MONOMETHYLMERCURY; BIOAVAILABILITY;
D O I
10.1016/j.envpol.2014.05.013
中图分类号
X [环境科学、安全科学];
学科分类号
08 ; 0830 ;
摘要
The present study demonstrates that species-specific isotope tracing is an useful tool to precisely measure Hg accumulation and transformations capabilities of living organisms at concentrations naturally encountered in the environment. To that end, a phytoplanktonic green alga Chlamydomonas reinhardtii Dangeard (Chlamydomonadales, Chlorophyceae) was exposed to mixtures of (199)-isotopically enriched inorganic mercury ((IHg)-I-199) and of (201)-isotopically enriched monomethylmercury ((CH3Hg)-C-201) at a concentration range between less than 1 pM to 4 nM. Additionally, one exposure concentration of both mercury species was also studied separately to evaluate possible interactive effects. No difference in the intracellular contents was observed for algae exposed to (IHg)-I-199 and (CH3Hg)-C-201 alone or in their mixture, suggesting similar accumulation capacity for both species at the studied concentrations. Demethylation of (CH3Hg)-C-201 was observed at the highest exposure concentrations, whereas no methylation was detected. (C) 2014 Elsevier Ltd. All rights reserved.
引用
收藏
页码:212 / 215
页数:4
相关论文
共 36 条
[1]   DISTRIBUTION OF MERCURY IN THE AQUATIC FOOD-WEB OF ONONDAGA LAKE, NEW-YORK [J].
BECKER, DS ;
BIGHAM, GN .
WATER AIR AND SOIL POLLUTION, 1995, 80 (1-4) :563-571
[2]  
Bjorn E, 2007, AMBIO, V36, P443, DOI 10.1579/0044-7447(2007)36[443:RAIMSA]2.0.CO
[3]  
2
[4]   Investigations into the differential reactivity of endogenous and exogenous mercury species in coastal sediments [J].
Bouchet, S. ;
Rodriguez-Gonzalez, P. ;
Bridou, R. ;
Monperrus, M. ;
Tessier, E. ;
Anschutz, P. ;
Guyoneaud, R. ;
Amouroux, D. .
ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, 2013, 20 (03) :1292-1301
[5]   Extremely elevated methyl mercury levels in water, sediment and organisms in a Romanian reservoir affected by release of mercury from a chlor-alkali plant [J].
Bravo, Andrea Garcia ;
Cosio, Claudia ;
Amouroux, David ;
Zopfi, Jakob ;
Cheualley, Pierre-Alain ;
Spangenberg, Jorge E. ;
Ungureanu, Viorel-Gheorghe ;
Dominik, Janusz .
WATER RESEARCH, 2014, 49 :391-405
[6]  
Campbell P.G.C., 1995, Metal Speciation and Bioavailability in Aquatic Systems, P45
[7]   Influence of dissolved organic matter character on mercury incorporation by planktonic organisms: An experimental study using oligotrophic water from Patagonian lakes [J].
Dieguez, Maria C. ;
Queimalinos, Claudia P. ;
Ribeiro Guevara, Sergio ;
Marvin-DiPasquale, Mark ;
Soto Cardenas, Carolina ;
Arribere, Maria A. .
JOURNAL OF ENVIRONMENTAL SCIENCES, 2013, 25 (10) :1980-1991
[8]   Mercury methylation in the hypolimnetic waters of lakes with and without connection to wetlands in northern Wisconsin [J].
Eckley, CS ;
Watras, CJ ;
Hintelmann, H ;
Morrison, K ;
Kent, AD ;
Regnell, O .
CANADIAN JOURNAL OF FISHERIES AND AQUATIC SCIENCES, 2005, 62 (02) :400-411
[9]   Influence of natural dissolved organic carbon on the bioavailability of mercury to a freshwater alga [J].
Gorski, P. R. ;
Armstrong, D. E. ;
Hurley, J. P. ;
Krabbenhoft, D. P. .
ENVIRONMENTAL POLLUTION, 2008, 154 (01) :116-123
[10]   Speciation of aqueous methylmercury influences uptake by a freshwater alga (Selenastrum capricornutum) [J].
Gorski, PR ;
Armstrong, DE ;
Hurley, JP ;
Shafer, MM .
ENVIRONMENTAL TOXICOLOGY AND CHEMISTRY, 2006, 25 (02) :534-540