K. Paul, Martijn Hermans, S. Jokinen, I. Brinkmann, H. Filipsson, T. Jilbert
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引用次数: 0
Abstract
Abstract. Sedimentary molybdenum (Mo) and uranium (U) enrichments are often used as redox proxies to reconstruct bottom water redox changes. However, these redox proxies may not be equally reliable across a range of coastal settings due to varying depositional environments. Fjords vary greatly in their depositional conditions, due to their unique bathymetry and hydrography, and are highly vulnerable to anthropogenic and climatic pressures. Currently, it is unknown to what extent Mo and U sequestration is affected by variable depositional conditions in fjords. Here, we use pore water and sequential extraction data to investigate Mo and U enrichment pathways in sediments of two sill fjords on the Swedish west coast with contrasting depositional environments and bottom water redox conditions. Our data suggest that sedimentary authigenic Mo and U pools differ between the two fjords. At the (ir)regularly dysoxic (oxygen = 0.2–2 mL L−1) Gullmar Fjord, authigenic Mo largely binds to manganese (Mn) oxides and to a lesser extent to iron (Fe) oxides; Mo sulfides do not play a major role due to low sulfate reduction rates, which limits the rate of Mo burial. Authigenic U largely resides in carbonates. At the (ir)regularly euxinic (oxygen = 0 mL L−1; total hydrogen sulfide ≥ 0 mL L−1) Koljö Fjord, authigenic Mo is significantly higher due to binding with more refractory organic matter complexes and Mo-Fe-sulfide phases. Uranium is moderately enriched and largely bound to organic matter. We found no direct evidence for temporal changes in bottom water redox conditions reflected in Mo and U enrichments at either Gullmar Fjord or Koljö Fjord. While sulfidic bottom waters favor Mo sequestration at Koljö Fjord, enrichment maxima reflect a combination of depositional conditions rather than short-term low-oxygen events. Our data demonstrate that secondary pre- and post-depositional factors control Mo and U sequestration in fjords to such an extent that bottom water redox conditions are either not being systematically recorded or overprinted. This explains the large variability in trace metal enrichments observed in fjords and has implications for applying Mo and U as proxies for environmental redox reconstructions in such systems.
摘要。沉积钼(Mo)和铀(U)富集度通常被用作氧化还原代用指标,以重建底层水氧化还原变化。然而,由于沉积环境的不同,这些氧化还原代用指标在不同的沿岸环境中可能并不同样可靠。峡湾由于其独特的水深和水文地理环境,沉积条件差异很大,极易受到人为和气候压力的影响。目前,钼和铀的固碳在多大程度上受到峡湾多变沉积条件的影响还不得而知。在这里,我们利用孔隙水和连续萃取数据研究了瑞典西海岸两个峡湾沉积物中钼和铀的富集途径,这两个峡湾的沉积环境和底水氧化还原条件截然不同。我们的数据表明,两个峡湾的沉积自生钼和铀池各不相同。在(非)经常缺氧(氧=0.2-2 mL L-1)的古尔马峡湾,自生钼主要与锰(Mn)氧化物结合,其次与铁(Fe)氧化物结合;由于硫酸盐还原率低,钼硫化物不起主要作用,这限制了钼的埋藏速度。自生铀主要存在于碳酸盐中。在(非)规则富氧(氧= 0 mL L-1;总硫化氢≥ 0 mL L-1)的科尔约峡湾,由于与较难分解的有机物复合物和钼-铁-硫化物相结合,自生钼含量明显较高。铀的富集程度适中,主要与有机物结合。在古尔马峡湾和科尔约峡湾,我们都没有发现底层水氧化还原条件随时间发生变化的直接证据,这反映在钼和铀的富集程度上。虽然硫酸底水有利于钼在科尔约峡湾的固着,但富集的最大值反映了沉积条件的综合变化,而不是短期的低氧事件。我们的数据表明,沉积前和沉积后的次要因素控制着峡湾中钼和铀的螯合,以至于底层水氧化还原条件要么未被系统记录,要么被覆盖。这就解释了在峡湾中观察到的痕量金属富集的巨大差异,并对在这类系统中应用钼和铀作为环境氧化还原重建的代用指标产生了影响。
期刊介绍:
Biogeosciences (BG) is an international scientific journal dedicated to the publication and discussion of research articles, short communications and review papers on all aspects of the interactions between the biological, chemical and physical processes in terrestrial or extraterrestrial life with the geosphere, hydrosphere and atmosphere. The objective of the journal is to cut across the boundaries of established sciences and achieve an interdisciplinary view of these interactions. Experimental, conceptual and modelling approaches are welcome.