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首页> 外文期刊>Environmental Science: Nano >Influence of multi-walled carbon nanotubes and fullerenes on the bioaccumulation and elimination kinetics of phenanthrene in geophagous earthworms (Metaphire guiUelmi)^
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Influence of multi-walled carbon nanotubes and fullerenes on the bioaccumulation and elimination kinetics of phenanthrene in geophagous earthworms (Metaphire guiUelmi)^

机译:多壁碳纳米管和富勒烯对冰水百科菲生物累积和消除动力学的影响(梅花Guiuelmi)^

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摘要

The impact of multi-walled carbon nanotubes (outer diameter <8 nm: MW8; >50 nm: MW50) and fullerene (C_(60)) at 300 or 3000 mg kg~(-1) on phenanthrene bioaccumulation and elimination kinetics (L, 1.37 mg kg~(-1); H, 16.14 mg kg"1) in a geophagous earthworm (Metaphire guillelmi) was investigated. Prior to worm exposure, the residual phenanthrene concentrations in soil decreased by 56.4% (L) and 59.9% (H) after 12 h of equilibrium. Phenanthrene accumulation in earthworms exhibited a bell-shaped pattern for all treatments. However, both the rate and extent of bioaccumulation and elimination were significantly affected by the CNMs, dependent on both the type and amendment level. C_(60) and MW8 at 300 mg kg~(-1) in the L system significantly decreased the uptake rate of phenanthrene, resulting in delayed maximum accumulation at 2 d. All other treatments had little impact on the uptake rate, with the exception of a slight decrease induced by MW8 at 3000 mg kg~(-1) The maximum phenanthrene accumulation followed an order of C_(60) > MW8 > MW50 at each amendment level of these materials. All CNMs increased the uptake rate of phenanthrene by earthworms in the H system, with the exception of MW8 at 3000 mg kg~(-1) where the maximum accumulation occurred earlier than the control. Furthermore, the uptake rate and maximum accumulation of phenanthrene in earthworms followed an order of C_(60) > MW50 > MW8 at each level, which was the opposite of its strength of sorption to these materials. Interestingly, phenanthrene bioaccumulation in the H system amended with 3000 mg kg"1 MW8 was 2.2-3.9 times that of all the other treatments at 35 d. For elimination, MW8 at this level increased phenanthrene amounts remaining in earthworms in both L (1.4-3.2 times) and H (1.1-15.2 times) systems. A higher burden of phenanthrene during the later bioaccumulation and elimination periods could result from ingestion and absorption of MW8; the accumulated phenanthrene may strongly bind to the internalized MW8, thereby reducing its elimination. Soil amendment with C_(60) and MW50 at both levels and MW8 at 300 mg kg~(-1) increased worm phenanthrene elimination in the L system, while that in the H system was not significantly affected. The results highlight the impact of CNMs on the bioaccumulation and elimination kinetics of phenanthrene in a typical geophagous earthworm, and provide important information for understanding of the potential risks of CNMs released into terrestrial systems.
机译:多壁碳纳米管(外径<8nm:mw8; 50nm:mw50)和富勒烯(c_(60))的影响在300或3000mg kg〜(-1)上对菲生物累积和消除动力学(l ,1.37mg kg〜(-1); h,16.14mg kg“1)在冰水蚯蚓(梅皮肖Guillelmi)中进行了调查。在蠕虫暴露之前,土壤中残留的菲浓度降低56.4%(L)和59.9% (h)在12小时后平衡。蚯蚓中的菲积累呈所有治疗的钟形图案。然而,生物累积和消除的速率和程度受到CNMS的显着影响,取决于类型和修正水平。 L系统中300mg kg〜(-1)的C_(60)和mw8显着降低了菲的摄取率,导致2天的最大累积延迟。所有其他治疗对摄取率几乎没有影响,但除了例外MW8在3000mg kg〜(-1)的最大菲丙烯AC诱导的轻微减少累积在这些材料的每个修正水平下进行了C_(60)> MW8> MW50的顺序。所有CNMS通过H系统中的蚯蚓增加了菲的摄取率,除了3000mg kg〜(-1)的MW8外,其中最大累积比控制更早发生。此外,蚯蚓中菲的摄取率和最大累积在每个水平下的C_(60)> Mw50> Mw8的顺序,这与其对这些材料的吸附强度相反。有趣的是,用3000毫克kg“1 mw8的H系统中的菲生物累积为35 d的所有其他治疗的2.2-3.9倍。对于消除,在L(1.4- 3.2次)和H(1.1-15.2次)系统。在后期生物累积和消除期间菲负担的菲负担可能是由于摄入和吸收MW8;累积的菲恩甲烷可能与内化MW8强烈结合,从而减少其消除。用C_(60)和MW50的土壤修正为300mg kg〜(-1)增加L系统中的蠕虫菲消除蠕虫菲消除,而H系统的影响不会受到显着影响。结果突出了CNMS的影响论典型的泻蚯蚓菲的生物累积和消除动力学,提供了解释放到陆地系统中CNMS潜在风险的重要信息。

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  • 来源
    《Environmental Science: Nano》 |2017年第9期|共13页
  • 作者单位

    Laboratory for Earth Surface Processes College of Urban and Environmental Sciences Peking University Beijing 100871 China;

    Laboratory for Earth Surface Processes College of Urban and Environmental Sciences Peking University Beijing 100871 China;

    Laboratory for Earth Surface Processes College of Urban and Environmental Sciences Peking University Beijing 100871 China;

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  • 原文格式 PDF
  • 正文语种 eng
  • 中图分类 环境科学、安全科学;
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