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Photochemistry of marine and fresh waters: A role for copper-dissolved organic matter ligands

机译:海洋和淡水的光化学:溶解铜的有机物配体的作用

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The photodegradation of marine dissolved organic matter (DOM) plays a critical role in the global carbon cycle. The photodegradation of both DOM and particulate organic matter (POM) leads to the formation of carbon monoxide and/or the production of labile organic matter that can be rapidly biodegraded. DOM also regulates metal speciation, particularly important for the bioavailability of nutrient metals required by phytoplankton. Copper is one of these essential nutrients but is also toxic in elevated concentrations. Its speciation is regulated by DOM photodegradation however, DOM-copper ligands are not well characterized because of their low concentrations in natural waters. Copper immobilized metal affinity chromatography (IMAC) was used to isolate high and low affinity DOM ligands from both Pacific near-shore seawater and freshwater from the Black River (NC). Laser flash photolysis (LFP) was used to characterize excited state species from these fractions and to identify excited state species in the open ocean through a depth profile from 5 to 4532 m (North Atlantic, Bermuda Atlantic Time Series Station (BATS)). LFP generated transients characteristic of the solvated electron (t = 3.5 ± 0.1 μs), a microbial-sourced triplet excited state (t = 1.1 μs ± 0.1 μs), and a long-lived transient, DOM*, with a millisecond lifetime. Unlike the seawater triplet excited state, a copper ligand from Black River water generated a triplet excited state with a lifetime of 3.4 ± 0.1 μs. Fractions were also characterized by excitation-emission matrix fluorescence spectroscopy (EEMs), UV-visible, and ~1H NMR spectroscopy. EEMs spectra correlated the marine excited state species with the protein-like, microbiai fraction while the freshwater transients were associated with chromophoric DOM (CDOM). ~1H NMR with spectral database matching identified ninety-seven compounds as potential sources of these excited state species in the Pacific seawater IMAC fractions. Aqueous extracts of marine macro-algae (Sargassum natans (Atlantic Ocean), Macrocystis pyrifera), and surf grass (Phyttospadix torreyi) were analyzed to investigate potential additional sources of these excited state transients. To our knowledge, this is the first study to characterize DOM-copper ligands in seawater using a combination of EEMs, NMR and laser flash photolysis.
机译:海洋溶解有机物(DOM)的光降解在全球碳循环中起着至关重要的作用。 DOM和颗粒有机物(POM)的光降解会导致一氧化碳的形成和/或可快速生物降解的不稳定有机物的产生。 DOM还调节金属形态,这对于浮游植物所需的营养金属的生物利用度尤其重要。铜是这些必需营养素之一,但在高浓度下也有毒。它的形态受到DOM光降解的调节,但是,由于DOM-铜配体在天然水中的浓度低,因此无法很好地表征。铜固定金属亲和色谱法(IMAC)用于从太平洋近岸海水和黑河(NC)的淡水中分离高亲和力和低亲和力的DOM配体。激光闪光光解法(LFP)用于表征这些馏分中的激发态物种,并通过5至4532 m的深度剖面(北大西洋,百慕大大西洋时间序列站(BATS))来识别公海中的激发态物种。 LFP产生了溶剂化电子的瞬态特征(t = 3.5±0.1μs),微生物源的三重态激发态(t = 1.1μs±0.1μs)和长寿命的DOM *,具有毫秒级的寿命。与海水的三重态激发态不同,黑河水中的铜配体产生了三重态激发态,寿命为3.4±0.1μs。还通过激发发射矩阵荧光光谱(EEM),紫外可见光谱和〜1H NMR光谱对馏分进行表征。 EEMs谱图将海洋激发态物种与蛋白质样微生物偏置相关,而淡水瞬态与发色DOM(CDOM)相关。约1H NMR与光谱数据库匹配确定了97种化合物是太平洋海水IMAC馏分中这些激发态物种的潜在来源。分析了海洋大型藻类(Sargassum natans(大西洋),Macrocystis pyrifera)和冲浪草(Phyttospadix torreyi)的水提物,以研究这些激发态瞬态的潜在其他来源。据我们所知,这是首次结合EEM,NMR和激光闪光光解法表征海水中DOM-铜配体的研究。

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