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河流源腐殖质作为海水中的铁螯合剂

River-derived humic substances as iron chelators in seawater.

作者信息

Krachler Regina, Krachler Rudolf F, Wallner Gabriele, Hann Stephan, Laux Monika, Cervantes Recalde Maria F, Jirsa Franz, Neubauer Elisabeth, von der Kammer Frank, Hofmann Thilo, Keppler Bernhard K

机构信息

Institute of Inorganic Chemistry, University of Vienna, Währingerstraße 42, 1090 Vienna, Austria.

Division of Analytical Chemistry, University of Natural Resources and Life Sciences, Vienna, Muthgasse 18, 1190 Vienna, Austria.

出版信息

Mar Chem. 2015 Aug 20;174:85-93. doi: 10.1016/j.marchem.2015.05.009.

Abstract

The speciation of iron(III) in oxic seawater is dominated by its hydrolysis and sedimentation of insoluble iron(III)-oxyhydroxide. As a consequence, many oceanic areas have very low iron levels in surface seawater which leads to iron deficiency since phytoplankton require iron as a micronutrient in order to grow. Fortunately, iron solubility is not truly as low as Fe(III) solubility measurements in inorganic seawater would suggest, since oceanic waters contain organic molecules which tend to bind the iron and keep it in solution. Various iron-binding organic ligands which combine to stabilize dissolved iron have been detected and thoroughly investigated in recent years. However, the role of iron-binding ligands from terrestrial sources remains poorly constrained. Blackwater rivers supply large amounts of natural organic material (NOM) to the ocean. This NOM (which consists mainly of vascular plant-derived humic substances) is able to greatly enhance iron bioavailability in estuaries and coastal regions, however, breakdown processes lead to a rapid decrease of river-derived NOM concentrations with increasing distance from land. It has therefore been argued that the influence of river-derived NOM on iron biogeochemistry in offshore seawater does not seem to be significant. Here we used a standard method based on Fe as a radiotracer to study the solubility of Fe(III)-oxyhydroxide in seawater in the presence of riverine NOM. We aimed to address the question how effective is freshwater NOM as an iron chelator under open ocean conditions where the concentration of land-derived organic material is about 3 orders of magnitude smaller than in coastal regions, and does this iron chelating ability vary between NOM from different sources and between different size fractions of the river-borne NOM. Our results show that the investigated NOM fractions were able to substantially enhance Fe(III)-oxyhydroxide solubility in seawater at concentrations of the NOM ≥ 5 μg L. Terrigenous NOM concentrations ≥ 5 μg L are in no way unusual in open ocean surface waters especially of the Arctic and the North Atlantic Oceans. River-derived humic substances could therefore play a greater role as iron carriers in the ocean than previously thought.

摘要

在有氧海水中,铁(III)的形态主要由其水解以及不溶性氢氧化铁(III)的沉淀所主导。因此,许多海洋区域表层海水中的铁含量极低,这导致了缺铁现象,因为浮游植物生长需要铁作为微量营养素。幸运的是,铁的溶解度并非真的如无机海水中铁(III)溶解度测量结果所显示的那么低,因为海水中含有有机分子,这些有机分子倾向于与铁结合并使其保持在溶液中。近年来,已检测并深入研究了各种结合铁的有机配体,它们共同作用以稳定溶解态的铁。然而,来自陆地源的结合铁配体的作用仍知之甚少。黑水河流向海洋输送大量天然有机物质(NOM)。这种NOM(主要由维管植物衍生的腐殖物质组成)能够极大地提高河口和沿海地区铁的生物可利用性,然而,随着离陆地距离的增加,分解过程导致源自河流的NOM浓度迅速降低。因此,有人认为源自河流的NOM对近海海水中铁生物地球化学的影响似乎并不显著。在此,我们使用基于铁作为放射性示踪剂的标准方法,研究在存在河流NOM的情况下海水中氢氧化铁(III)的溶解度。我们旨在解决以下问题:在开阔海洋条件下,淡水NOM作为铁螯合剂的效果如何,此时源自陆地的有机物质浓度比沿海地区小约3个数量级,并且这种铁螯合能力在不同来源的NOM之间以及河流携带的NOM的不同粒径部分之间是否存在差异。我们的结果表明,在所研究的NOM浓度≥5μg/L时,NOM组分能够显著提高海水中氢氧化铁(III)的溶解度。陆源NOM浓度≥5μg/L在开阔海洋表层水体中并非罕见,尤其是在北极和北大西洋。因此,源自河流的腐殖物质在海洋中作为铁载体可能比以前认为的发挥更大的作用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d602/4567045/437cd46583b7/gr1.jpg

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