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铁同位素揭示了南大洋中层与深层不同的溶解铁来源和路径。

Iron isotopes reveal distinct dissolved iron sources and pathways in the intermediate versus deep Southern Ocean.

作者信息

Abadie Cyril, Lacan Francois, Radic Amandine, Pradoux Catherine, Poitrasson Franck

机构信息

LEGOS, University of Toulouse, CNRS, CNES, IRD, UPS, 31400 Toulouse, France.

LEGOS, University of Toulouse, CNRS, CNES, IRD, UPS, 31400 Toulouse, France;

出版信息

Proc Natl Acad Sci U S A. 2017 Jan 31;114(5):858-863. doi: 10.1073/pnas.1603107114. Epub 2017 Jan 17.

Abstract

As an essential micronutrient, iron plays a key role in oceanic biogeochemistry. It is therefore linked to the global carbon cycle and climate. Here, we report a dissolved iron (DFe) isotope section in the South Atlantic and Southern Ocean. Throughout the section, a striking DFe isotope minimum (light iron) is observed at intermediate depths (200-1,300 m), contrasting with heavier isotopic composition in deep waters. This unambiguously demonstrates distinct DFe sources and processes dominating the iron cycle in the intermediate and deep layers, a feature impossible to see with only iron concentration data largely used thus far in chemical oceanography. At intermediate depths, the data suggest that the dominant DFe sources are linked to organic matter remineralization, either in the water column or at continental margins. In deeper layers, however, abiotic non-reductive release of Fe (desorption, dissolution) from particulate iron-notably lithogenic-likely dominates. These results go against the common but oversimplified view that remineralization of organic matter is the major pathway releasing DFe throughout the water column in the open ocean. They suggest that the oceanic iron cycle, and therefore oceanic primary production and climate, could be more sensitive than previously thought to continental erosion (providing lithogenic particles to the ocean), particle transport within the ocean, dissolved/particle interactions, and deep water upwelling. These processes could also impact the cycles of other elements, including nutrients.

摘要

作为一种必需的微量营养素,铁在海洋生物地球化学中起着关键作用。因此,它与全球碳循环和气候相关联。在此,我们报告了南大西洋和南大洋的溶解铁(DFe)同位素剖面。在整个剖面中,在中间深度(200 - 1300米)观察到显著的DFe同位素最小值(轻铁),这与深层水中较重的同位素组成形成对比。这明确表明了在中间层和深层中,不同的DFe来源和过程主导着铁循环,这一特征是仅使用化学海洋学中迄今大量使用的铁浓度数据所无法看到的。在中间深度,数据表明主要的DFe来源与水柱中或大陆边缘的有机物再矿化有关。然而,在更深的层中,铁从颗粒态铁(特别是岩石源的)的非生物非还原释放(解吸、溶解)可能占主导地位。这些结果与普遍但过于简单的观点相悖,即有机物再矿化是公海中整个水柱释放DFe的主要途径。它们表明海洋铁循环以及因此海洋初级生产力和气候可能比以前认为的对大陆侵蚀(向海洋提供岩石源颗粒)、海洋内部的颗粒运输、溶解/颗粒相互作用以及深水上升流更为敏感。这些过程也可能影响包括营养物质在内的其他元素的循环。

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