More than inorganic copper is bioavailable to aquatic mosses at environmentally relevant concentrations

被引:35
作者
Ferreira, Daniel [1 ]
Tousset, Nicolas [1 ]
Ridame, Celine [2 ]
Tusseau-Vuillemin, Marie-Helene [3 ]
机构
[1] Elect France, Dept Natl Hydraul & Environm, Div Rech & Dev, F-78401 Chatou, France
[2] Univ Paris 06, Lab Oceanog & Climat Expt & Approches Numer, F-75252 Paris 5, France
[3] Cemagref, UR HBAN, F-92163 Antony, France
关键词
aquatic mosses; diffusion gradient/thin films; bioaccumulation kinetics; lability; copper;
D O I
10.1897/07-249.1
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 investigates how dissolved organic matter (DOM) alters copper bioavailability at environmentally relevant concentrations (1 - 5 mu g/L of dissolved copper, 1 - 4 mg/L of dissolved organic copper). A methodology combining two biological endpoints (short-term and steady-state bioaccumulation of copper by the aquatic moss Fontinalis antipyretica) and a sampling of labile copper with diffusion gradient in thin films (DGT) is proposed for batch experiments conducted with mineral water and various DOM, ethylenediaminetetra-acetic acid (EDTA), humic acid, and natural Seine River (France) extracts (hydrophobic and transphilic fractions). All types of DOM reduce the bioavailability of copper to aquatic mosses, and this reduction was more pronounced for the short-term biological endpoint, which was taken as being representative for environmental exposure. Labile copper sampled with DGT made it possible to estimate short-term bioaccumulation in the case of EDTA and natural Seine River extracts. With humic acid solutions, however, labile copper was lower than bioavailable copper. This result suggests that at realistic metal concentrations and with certain types of natural DOM, bioavailable copper might comprise not only inorganic copper but also some weak organic complexes. Hence, labile copper, in situ sampled with DGT, might not systematically overestimate bioavailable copper, as suggested previously on the basis of in vitro toxicity studies.
引用
收藏
页码:2108 / 2116
页数:9
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