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首页> 外文期刊>Oceanographic Literature Review >Sedimentary cycling and benthic fluxes of manganese, cobalt, nickel, copper, zinc and cadmium in the Peruvian oxygen minimum zone
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Sedimentary cycling and benthic fluxes of manganese, cobalt, nickel, copper, zinc and cadmium in the Peruvian oxygen minimum zone

机译:铀氧气最小区域沉积物,钴,镍,铜,锌和镉的沉积循环和底栖助焊剂

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摘要

Marine sediments are an important source and sink of bio-essential trace metals to the ocean. However, the different mechanisms leading to trace metal release or burial are not fully understood and the associated fluxes are not well quantified. Here, we present sediment, pore water, sequential extraction and benthic flux data of Mn, Co, Ni, Cu, Zn and Cd along a latitudinal depth transect across the Peruvian oxygen minimum zone at 12°S. Sediments are depleted in Mn and Co compared to the lithogenic background. Diffusive Mn fluxes from the sediments into the bottom water (-26 to -550 μmol m~(-2) y~(-1)) are largely consistent with the rate of Mn loss from the solid phase (-100 to -1160 μmol m~(-2) yr~(-1)) suggesting that 50% or more of the sedimentary Mn depletion is attributed to benthic efflux. In contrast, benthic Co fluxes (~ -3 μmol m~(-2) yr~(-1)) are lower than the rate of Co loss from the solid phase (up to -120 μmol m~(-2) yr~(-1)), implying Co dissolution in the water column. The trace metals Ni, Cu, Zn and Cd are enriched within the sediments with respect to the lithogenic background. Uptake of Ni by phytoplankton in the photic zone and delivery with organic matter to the sediment surface can account for up to 100% of the excess Ni accumulation (87 to 180 μmol m~(-2) y~(-1)) in shelf sediments near the coast, whereas at greater water depth additional scavenging by Mn- and Fe-oxides may contribute to Ni accumulation. Up to 20% of excess Cu (33 to 590 μmol m~(-2) y~(-1)) and generally less than 20% of excess Zn (58 to 2170 μmol m~(-2) y~(-1)) and Cd (6 to 260 μmol m~(-2) y~(-1)) can be explained by delivery with fresh organic matter. Sequential extraction data suggest that the discrepancies between the known sources of Cd (and Cu) and their excess accumulation may be driven by the delivery of allo-chthonous sulphide minerals precipitated from the water column. Additionally, Cu may be scavenged by downward sinking organic material. In contrast, precipitation of Zn sulphide chiefly takes place in the sediment. Diffusive Zn fluxes into the sediment (21 to 1990 μmol m~(-2) y~(-1)) match the excess Zn accumulation suggesting that Zn delivery is mediated by molecular diffusion from bottom waters. Considering the diverse behavioural pattern of trace metals observed in this study, we argue that declining oxygen and increasing hydrogen sulphide concentrations in a future ocean will modify trace metal fluxes at the seafloor and the trace metal stoichiometry of seawater.
机译:海洋沉积物是海洋生物必需痕量金属的重要来源和汇。然而,导致痕量金属释放或埋葬的不同机制不完全理解,并且相关的助熔剂不充分定量。这里,我们沿12°S的秘密氧气最小区延伸延伸深度横跨潜水深度横跨潜水深度横跨潜水深度横跨沉积物,孔隙水,序列提取和CD的沉积物,孔隙水,序列提取和底焊剂数据。与岩石背景相比,沉积物耗尽Mn和Co。从沉积物中的扩散Mn助熔剂进入底部水(-26至-550μmolm〜(-2)y〜(-1))主要是与固相的Mn损耗(-100至-1160μmol的速率一致M〜(-2)Yr〜(-1))表明50%或更多的沉积Mn耗尽归因于底栖渗透。相反,底栖Co助熔剂(〜-3μmolm〜(-2)Yr〜(-1))低于来自固相的CO损失的速率(高达-120μmolm〜(-2)Yr〜 (-1)),暗示水柱中的CO溶解。痕量金属Ni,Cu,Zn和Cd相对于岩性背景富含沉积物。通过浮游区的浮游植物吸收,并用有机物质递送到沉积物表面可以占架子上的多达100%的过度Ni积聚(87至180μmolm〜(-2)Y〜(-2)〜(-2))海岸附近的沉积物,而在较大的水深在额外的水深通过Mn-和Fe氧化物的清除可能有助于Ni积累。多达20%的过量Cu(33至590μmolm〜(-2)y〜(-1)),通常小于20%的过量Zn(58至2170μmolm〜(-2)y〜(-1 ))和Cd(6至260μmolm〜(-2)y〜(-1))可以通过新鲜有机物递送来解释。顺序提取数据表明,可以通过从水塔沉淀的血清硫化硫化物矿物的递送来驱动已知Cd(和Cu)和其过量积累之间的差异。另外,Cu可以通过向下沉降的有机材料清除。相反,Zn硫化物的沉淀主要发生在沉积物中。将Zn通量扩散到沉积物中(21至1990μmolM〜(-2)y〜(-1))匹配,过量Zn积累表明Zn递送是通过来自底部水分子扩散介导的。考虑到本研究中观察到的痕量金属的多样化行为模式,我们认为未来海洋中的氧气下降和增加硫化氢浓度将在海底和海水的痕量金属化学计量中修改痕量金属助熔剂。

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  • 来源
    《Oceanographic Literature Review》 |2021年第7期|1477-1477|共1页
  • 作者

    A. Plass; A.W. Dale; F. Scholz;

  • 作者单位

    GEOMAR Helmholtz Centre for Ocean Research Kiel Wischhofstrasse 1-3 Kiel 24148 Germany;

    GEOMAR Helmholtz Centre for Ocean Research Kiel Wischhofstrasse 1-3 Kiel 24148 Germany;

    GEOMAR Helmholtz Centre for Ocean Research Kiel Wischhofstrasse 1-3 Kiel 24148 Germany;

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