Felgate Stacey L, Jakobsson Elizabeth, Balderrama Subieta Andrea, Tranvik Lars J, Hawkes Jeffrey A
Department of Chemistry, Uppsala University, Uppsala 751 23, Sweden.
Department of Ecology and Evolution, Uppsala University, Uppsala 752 36, Sweden.
J Am Soc Mass Spectrom. 2024 Dec 4;35(12):2910-2917. doi: 10.1021/jasms.4c00255. Epub 2024 Oct 5.
Dissolved organic matter (DOM) is a complex mixture of thousands of molecular formulas comprised of an unknown number of chemical compounds, the concentration and composition of which are critical to ecosystem function and biogeochemical cycling. Despite its importance, our understanding of the DOM composition is lacking. This is principally due to its molecular complexity, which means that no single method is capable of describing DOM in its entirety. Quantification is typically done by proxy (e.g., relative to carbon content) and does not necessarily match well to compositional data, due to incomplete analytical windows and selectivity of different analytical methods. We present an integrated liquid chromatography (LC)-diode array detector (DAD)-charged aerosol detector (CAD)-mass spectrometry (MS) pipeline designed to both characterize and quantify solid-phase extractable DOM (SPE-DOM) in a single analysis. We applied this method to a set of eight Swedish water bodies sampled in the summer and winter. Chromophoric SPE-DOM was proportionally higher in samples with higher SPE-DOM concentrations but remained relatively consistent between sampling occasions. Ionizable SPE-DOM was relatively consistent across sites but was proportionally higher in summer. Overall, the carbon content of DOM was very consistently ∼40% across sites in both summer and winter. These findings suggest that SPE-DOM concentration at these sites is driven by (presumably allochthonous) chromophoric inputs, with an increased relative contribution in summer of material that is more ionizable and less chromophoric and may be either autochthonous or selectively enriched from allochthonous sources. Thus, with minimal additional effort, this method provided further compositional insights not attained by any single analysis in isolation.
溶解有机物(DOM)是由数千种分子式组成的复杂混合物,包含数量未知的化合物,其浓度和组成对生态系统功能和生物地球化学循环至关重要。尽管其很重要,但我们对DOM组成的了解仍很欠缺。这主要是由于其分子复杂性,这意味着没有单一方法能够完整描述DOM。量化通常通过替代指标(例如相对于碳含量)进行,由于分析窗口不完整和不同分析方法的选择性,其不一定与组成数据匹配良好。我们提出了一种集成的液相色谱(LC)-二极管阵列检测器(DAD)-带电气溶胶检测器(CAD)-质谱(MS)流程,旨在在一次分析中同时表征和量化固相可萃取DOM(SPE-DOM)。我们将此方法应用于夏季和冬季采样的一组八个瑞典水体。发色SPE-DOM在SPE-DOM浓度较高的样品中比例更高,但在不同采样期间保持相对一致。可电离SPE-DOM在各采样点相对一致,但在夏季比例更高。总体而言,夏季和冬季各采样点DOM的碳含量非常一致,约为40%。这些发现表明,这些采样点的SPE-DOM浓度受(可能是外源的)发色输入驱动,夏季中更易电离且发色性较低的物质(可能是本地的或从外源选择性富集的)的相对贡献增加。因此,只需付出最小的额外努力,该方法就能提供单独任何一种分析都无法获得的进一步组成见解。