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Metal-solid interactions controlling the bioavailability of mercury from sediments to clams and sipunculans

机译:金属与固体之间的相互作用控制了汞从沉积物到蛤and和五倍子的生物利用度

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The bioavailability of sedimentary Hg(II) and methylmercury (MeHg) was quantified by measuring the assimilation efficiency (AE) in the clam Ruditapes philippinarum and the extraction of the gut juices from the sipunculan Sipunculus nudus. Three factors (Hg concentration in sediment, Hg sediment contact time, and organic content of sediments) were modified to examine metal-solid interactions in controlling Hg bioavailability. The Hg AEs in the clams were strongly correlated with the extraction from the sipunculan gut juices for both Hg species. The bioavailability of both Hg(II) and MeHg generally increased with increased sediment Hg concentration but decreased with sediment-metal contact time and increasing organic content (except that MeHg was not influenced by organic content). Hg(II) speciation in sediments, quantified by sequential chemical extraction (SCE), was dependent on geochemical conditions and greatly controlled the mobility and bioavailability of Hg(II) in sediments. Most bioavailable Hg(II) originated from the strongly complexed phase (e. g., Hg bound up in Fe/Mn oxide, amorphous organosulfur, or mineral lattice), whereas Hg bound with the organocomplexed phase (Hg humic and Hg2Cl2) was not bioavailable. Hg bound with the other geochemical phases (water soluble, HgO, HgSO4, and HgS) contributed very little to the bioavailable Hg due to their low partitionings. Further, the amount of bioavailable Hg was inversely related to the particle reactivity of Hg with the sediments. Detailed analyses of metal-solid interactions provide a better understanding of how Hg in sediments can predict Hg concentration and therefore bioavailability in benthic invertebrates.
机译:通过测量菲律宾蛤仔中的同化效率(AE)以及从西五味子Sipunculus nudus中提取肠液来量化沉积Hg(II)和甲基汞(MeHg)的生物利用度。修改了三个因素(沉积物中的Hg浓度,Hg沉积物接触时间和沉积物的有机含量),以检查金属与固体之间的相互作用,以控制Hg的生物利用度。蛤中的汞AE与两种汞物种从sipunculan肠汁中提取的含量密切相关。 Hg(II)和MeHg的生物利用度通常随沉积物Hg浓度的增加而增加,但随沉积物-金属接触时间和有机物含量的增加而降低(除了MeHg不受有机物含量的影响)。通过连续化学萃取(SCE)量化的沉积物中Hg(II)形态,取决于地球化学条件,并极大地控制了Hg(II)在沉积物中的迁移率和生物利用度。大多数可生物利用的Hg(II)均来自强络合相(例如,结合在Fe / Mn氧化物,无定形有机硫或矿物晶格中的Hg),而与有机络合相结合的Hg(腐殖质和Hg2Cl2)则不可生物利用。与其他地球化学相(水溶性,HgO,HgSO4和HgS)结合的Hg由于其分配低而对生物利用Hg的贡献很小。此外,可生物利用的汞量与汞与沉积物的颗粒反应性成反比。对金属-固体相互作用的详细分析可更好地了解沉积物中的汞如何预测汞浓度以及底栖无脊椎动物的生物利用度。

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