百慕大大西洋和夏威夷 ALOHA 时间序列站溶解有机物的光学特性和分子差异

IF 3.5 Q3 ENGINEERING, ENVIRONMENTAL Environmental science. Advances Pub Date : 2024-03-26 DOI:10.1039/D3VA00361B
Michael Gonsior, Madeline Lahm, Leanne Powers, Feng Chen, S. Leigh McCallister, Dong Liang, Grace Guinan and Philippe Schmitt-Kopplin
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摘要

光学活性成分,即海洋色度 DOM(CDOM)和荧光 DOM(FDOM),已被用作世界海洋中难溶解 DOM(RDOM)的代用指标,使用超高分辨率(HRMS)方法进行的大量研究提供了有关 DOM 化学复杂性和多样性的大量数据。在此,我们于 2019 年 8 月在北大西洋环流的百慕大大西洋时间序列研究(BATS)站,以及 2021 年 7 月在北太平洋环流的夏威夷海洋时间序列(HOT)使用的 ALOHA(长期低营养栖息地评估)站,收集并分析了整个水柱中 DOM 的高分辨率深度剖面图。从 BATS 的 4530 米和 ALOHA 的 4700 米至海面,以 200 米的深度间隔采集水样,并通过固相萃取(SPE)分离 DOM。对 EEM 荧光进行平行因子分析建模后发现,固相萃取-DOM 中的 "腐殖质类 "和 "蛋白质类 "FDOM(分别为 FDOMH 和 FDOMP)在整个水体中都发生了变化,其中 ALOHA 处的荧光强度较高。BATS SPE-DOM 中的溶解有机磷(DOP)和溶解有机硫(DOS)浓度始终高于 ALOHA,但 ALOHA 表层的 DOP 除外。负模式电喷雾离子化 (ESI) HRMS 数据也揭示了 BATS 和 ALOHA 之间的根本差异。我们采用了一种新颖的机器学习算法(SOFAR),发现 BATS 与 ALOHA 相比,主要差异在于 BATS 的总体氧碳(O/C)比分子特征要高得多,而且 BATS 的 DOS 特征也要高得多。此外,我们首次提取了弱阴离子交换(WAX)可修正 DOM,结果也显示了两个站点之间的巨大差异。光学数据和 HRMS 数据趋于一致,支持了这样一种观点,即通过这些分析窗口观察大西洋和太平洋盆地的 DOM,至少在这些长期监测站点是完全不同的。这一发现表明,在阿洛哈站和巴特斯站,海洋 DOM 的翻转速度可能不同,DOM 成分的地理差异可能是 DOM 反应性的一个复合因素。
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Optical properties and molecular differences in dissolved organic matter at the Bermuda Atlantic and Hawai'i ALOHA time-series stations†

Optically active components, namely marine chromophoric DOM (CDOM) and fluorescent DOM (FDOM), have been used as proxies for refractory DOM (RDOM) in the world's oceans, and numerous studies using ultrahigh resolution mass spectrometry (HRMS) approaches have supplied a tremendous amount of data on the chemical complexity and diversity of DOM. Here, we collected and analyzed high-resolution depth profiles of DOM throughout the water column in the North Atlantic Gyre at the Bermuda Atlantic Time-series Study (BATS) station in August 2019 and in the North Pacific Gyre at station ALOHA (A Long-term Oligotrophic Habitat Assessment) used by the Hawaii Ocean Time-series (HOT) in July 2021. Water samples were collected at 200 m depth intervals from 4530 m at BATS and 4700 m at ALOHA up to the surface and DOM was isolated by solid-phase extraction (SPE). Parallel factor analysis modeled EEM fluorescence revealed changes of “humic-like” and “protein-like” FDOM (FDOMH and FDOMP, respectively) in SPE-DOM throughout the water column with higher fluorescence intensities present at ALOHA. Dissolved organic phosphorous (DOP) and dissolved organic sulfur (DOS) concentrations were always higher in SPE-DOM at BATS than at ALOHA, except for DOP in the surface at ALOHA. Negative mode electrospray ionization (ESI) Fourier transform ion cyclotron resonance mass spectrometry (FT-ICR MS) data also revealed fundamental differences between BATS and ALOHA. A novel machine learning algorithm (SOFAR) was implemented and revealed much higher overall oxygen to carbon (O/C) ratio molecular signatures at BATS as the major difference and also much more DOS signatures at BATS when compared to ALOHA. Furthermore, we extracted for the first-time weak anion exchange (WAX) amendable DOM, and the results also showed drastic differences between the two stations. The optical and FT-ICR MS data, converged and supported the idea that DOM in the Atlantic and Pacific basins are fundamentally different when looked at through these analytical windows, at least at these long-term monitoring stations. This finding suggests that the marine DOM is likely turning over at different rates at ALOHA versus BATS and that geographical differences in DOM composition are likely a compounding factor in DOM reactivity.

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