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首页> 外文期刊>Marine Chemistry >Ultrahigh resolution mass spectrometric differentiation of dissolved organic matter isolated by coupled reverse osmosis-electrodialysis from various major oceanic water masses
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Ultrahigh resolution mass spectrometric differentiation of dissolved organic matter isolated by coupled reverse osmosis-electrodialysis from various major oceanic water masses

机译:通过反渗透-电渗析分离各种主要海洋水体中的溶解有机物的超高分辨率质谱分析

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摘要

A high-recovery technique of dissolved organic matter (DOM) isolation - reverse osmosis coupled with electro-dialysis (RO/ED) - was used to isolate DOM from the North Atlantic Senegal-Mauritanian upwelling area surface water (5 m), North Atlantic oxygen minimum water (415 m) and deep water (3000 m), North Pacific subtropical gyre surface water (5 m), and North Pacific intermediate water (674 m) and deep water (3500 m). Samples were characterized by ultrahigh resolution Fourier transform ion cyclotron resonance mass spectrometry with electrospray ionization (ESI FTICR-MS). RO/ED isolated DOM samples share a significant number of common formulas accounting for 54-79% of formulas in each sample. Total dissolved carbohydrate (TCHO) concentrations in RO/ED isolated DOM were specifically measured using a colorimetric method, and were found to have higher contribution to DOC than estimated by FTICR-MS data. Percentages of TCHO-C in DOC are in the range of 3.7-19.6% in all samples, with the North Pacific deep (3500 m) water having the lowest % and the North Atlantic up-welling core surface water having the highest %. Principal component analysis (PCA) using the relative magnitudes of MS peaks facilitated identification of specific peaks that are enriched in different samples. Peaks enriched in surface samples have higher H/C values than peaks enriched in deep samples, in both the North Atlantic DOM and the North Pacific DOM. This enrichment pattern is likely due to the selective photo-degradation of aromatic compounds and the bio-production of aliphatic and carbohydrate-like compounds in surface waters, and the selective bio-degradation of aliphatic and carbohydrate-like compounds with increasing depth. In further support of a photo-degraded signature for DOM in surface waters, photo-resistant and photo-produced molecular formulas were present in the highest numbers in the surface North Pacific subtropical gyre DOM. Peaks enriched in the North Pacific intermediate and deep DOM have significantly higher O/C values than the North Atlantic oxygen minimum layer and deep DOM, for both CHO formula compounds and CHON formula compounds. This difference in O/C values observed for the deep Pacific vs. Atlantic suggests oxidation of DOM, possibly via microbial activity during the ageing of DOM or the preferential remineralization of DOM from sinking particles at depth in the Pacific.
机译:溶解有机物(DOM)隔离的高回收技术-反渗透与电渗析(RO / ED)-用于从北大西洋塞内加尔-毛里塔尼亚上升流地表水(5 m)中分离出DOM最低氧气量(415 m)和深水(3000 m),北太平洋亚热带回旋地表水(5 m)和北太平洋中间水(674 m)和深水(3500 m)。通过超高分辨率傅里叶变换离子回旋共振质谱和电喷雾电离(ESI FTICR-MS)对样品进行表征。 RO / ED隔离的DOM样本共享大量的通用公式,占每个样本中公式的54-79%。使用比色法专门测量了RO / ED分离的DOM中总溶解碳水化合物(TCHO)的浓度,发现其对DOC的贡献比FTICR-MS数据估计的高。在所有样品中,TCHO-C的百分比在所有样品中都在3.7-19.6%的范围内,其中北太平洋深层(3500 m)水的百分比最低,而北大西洋上升流核心地表水的百分比最高。使用MS峰的相对幅度的主成分分析(PCA)有助于鉴定富集在不同样品中的特定峰。在北大西洋DOM和北太平洋DOM中,表面样品中富集的峰比深部样品中富集的峰具有更高的H / C值。这种富集模式可能是由于芳香化合物的选择性光降解以及地表水中脂肪族和类碳水化合物化合物的生物生产,以及脂肪族和类碳水化合物化合物随着深度的增加而选择性地生物降解。为了进一步支持地表水中DOM的光降解特征,在北太平洋亚热带回旋区DOM中,存在最高数量的抗光和光生分子式。对于CHO分子式和CHON分子式而言,富集在北太平洋中层和深层DOM中的峰的O / C值明显高于北大西洋最小氧层和深层DOM。在深太平洋和大西洋之间观察到的O / C值差异表明DOM可能通过DOM老化过程中的微生物活性或从太平洋深处沉没的颗粒优先矿化而导致DOM氧化。

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