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直接注入液相色谱-高分辨率质谱法测定冰芯中主要和次要的陆地和海洋生物标志物。

Direct Injection Liquid Chromatography High-Resolution Mass Spectrometry for Determination of Primary and Secondary Terrestrial and Marine Biomarkers in Ice Cores.

机构信息

British Antarctic Survey , High Cross, Madingley Road , Cambridge CB3 0ET , United Kingdom.

Department of Chemistry , University of Cambridge , Lensfield Road , Cambridge CB2 1EW , United Kingdom.

出版信息

Anal Chem. 2019 Apr 16;91(8):5051-5057. doi: 10.1021/acs.analchem.8b05224. Epub 2019 Mar 29.

DOI:10.1021/acs.analchem.8b05224
PMID:30893554
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC6536135/
Abstract

Many atmospheric organic compounds are long-lived enough to be transported from their sources to polar regions and high mountain environments where they can be trapped in ice archives. While inorganic components in ice archives have been studied extensively to identify past climate changes, organic compounds have rarely been used to assess paleo-environmental changes, mainly due to the lack of suitable analytical methods. This study presents a new method of direct injection high performance liquid chromatography-mass spectrometry (HPLC-MS) analysis, without the need of preconcentrating the melted ice, for the determination of a series of novel biomarkers in ice core samples indicative of primary and secondary terrestrial and marine organic aerosol sources. Eliminating a preconcentration step reduces contamination potential and decreases the required sample volume thus allowing a higher time resolution in the archives. The method is characterized by limits of detection (LODs) in the range of 0.01-15 ppb, depending on the analyte, and accuracy evaluated through an interlaboratory comparison. We find that many components in secondary organic aerosols (SOAs) are clearly detectable at concentrations comparable to those previously observed in replicate preconcentrated ice samples from the Belukha glacier, Russian Altai Mountains. Some compounds with low recoveries in the preconcentration steps are now detectable in samples with this new direct injection method significantly increasing the range of environmental processes and sources that become accessible for paleo-climate studies.

摘要

许多大气有机化合物具有足够长的寿命,可以从其来源运送到极地和高山环境中,在那里它们可以被捕获在冰档案中。虽然已经广泛研究了冰档案中的无机成分,以识别过去的气候变化,但有机化合物很少被用于评估古环境变化,主要是因为缺乏合适的分析方法。本研究提出了一种新的方法,即直接注入高效液相色谱-质谱(HPLC-MS)分析,无需浓缩融化的冰,即可测定冰芯样品中一系列新型生物标志物,这些标志物表明陆地和海洋有机气溶胶的原生和次生来源。消除浓缩步骤可减少污染的可能性并减少所需的样品量,从而使档案中的时间分辨率更高。该方法的检测限(LOD)范围为 0.01-15 ppb,取决于分析物,并且通过实验室间比较来评估准确性。我们发现,在可比浓度下,许多次生有机气溶胶(SOA)中的成分明显可检测到,这些浓度与先前在俄罗斯阿尔泰山脉别卢哈冰川的重复浓缩冰样本中观察到的浓度相当。在浓缩步骤中回收率较低的一些化合物现在可以用这种新的直接注入方法检测到,这显著增加了可用于古气候研究的环境过程和来源的范围。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/6536135/62d1d2e0ff28/ac-2018-05224y_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/6536135/e0d9ea9501c9/ac-2018-05224y_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/6536135/62d1d2e0ff28/ac-2018-05224y_0003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/6536135/e0d9ea9501c9/ac-2018-05224y_0002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d1ff/6536135/62d1d2e0ff28/ac-2018-05224y_0003.jpg

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