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Using Compound-Specific and Bulk Stable Isotope Analysis for Trophic Positioning of Bivalves in Contaminated Baltic Sea Sediments

机译:使用特定化合物和大块稳定同位素分析技术对受污染的波罗的海沉积物中双壳类的营养定位

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摘要

Stable nitrogen isotopes (δ~(15)N) are used as indicators of trophic position (TP) of consumers. Deriving TP from δ~(15)N of individual amino acids (AAs) is becoming popular in ecological studies, because of lower uncertainty than TP based on bulk δ~(15)N (TP_(bulk)). This method would also facilitate biomagnification studies provided that isotope fractionation is unaffected by toxic exposure. We compared TP_(AA) and TP_(bulk) estimates for a sediment-dwelling bivalve from two coastal sites, a pristine and a contaminated. Chemical analysis of PCB levels in mussels, sediments, and pore water confirmed the expected difference between sites. Both methods, but in particular the TP_(AA) underestimated the actual TP of bivalves. Using error propagation, the total uncertainty related to the analytical precision and assumptions in the TP calculations was found to be similar between the two methods. Interestingly, the significantly higher intercept for the regression between TP_(AA) and TP_(bulk) in the contaminated site compared to the pristine site indicates a higher deamination rate due to detoxification as a result of chronic exposure and a higher ~(15)N fractionation. Hence, there is a need for controlled experiments on assumptions underlying amino acid-specific stable isotope methods in food web and bimagnification studies.
机译:稳定的氮同位素(δ〜(15)N)被用作消费者的营养位置(TP)的指标。从单个氨基酸(AAs)的δ〜(15)N推导TP在生态学研究中变得越来越普遍,因为其不确定性低于基于大量δ〜(15)N的TP(TP_(bulk))。如果同位素分离不受毒物暴露的影响,则该方法也将有助于生物放大研究。我们比较了来自两个沿海站点(原始和受污染)的沉积物双壳类动物的TP_(AA)和TP_(bulk)估计。对贻贝,沉积物和孔隙水中PCB含量的化学分析证实了预期的位点之间的差异。两种方法,特别是TP_(AA)均低估了双壳类动物的实际TP。使用误差传播,发现两种方法中与分析精度和TP计算假设有关的总不确定性相似。有趣的是,与原始位点相比,受污染位点中TP_(AA)和TP_(bulk)之间的回归截距显着更高,这表明由于长期暴露导致的排毒和更高的〜(15)N,使去氨率更高。分馏。因此,需要对食物网和双倍放大研究中特定于氨基酸的稳定同位素方法的假设进行对照实验。

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  • 来源
    《Environmental Science & Technology》 |2018年第8期|4861-4868|共8页
  • 作者单位

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden;

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden;

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden;

    Mass Spectrometry Laboratory, Center for Physical Science and Technology, Savanoriu 231, LT-02300 Vilnius, Lithuania;

    Mass Spectrometry Laboratory, Center for Physical Science and Technology, Savanoriu 231, LT-02300 Vilnius, Lithuania;

    Mass Spectrometry Laboratory, Center for Physical Science and Technology, Savanoriu 231, LT-02300 Vilnius, Lithuania;

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden;

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden;

    Department of Environmental Science and Analytical Chemistry, Stockholm University, Svante Arrhenius väg 8, SE-106 91 Stockholm, Sweden,Department of Ecology, Environment and Plant Science, Stockholm University, Svante Arrhenius väg 20, SE-114 18 Stockholm, Sweden;

  • 收录信息 美国《科学引文索引》(SCI);美国《工程索引》(EI);美国《生物学医学文摘》(MEDLINE);美国《化学文摘》(CA);
  • 原文格式 PDF
  • 正文语种 eng
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  • 入库时间 2022-08-17 13:56:41

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