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首页> 外文期刊>Geochimica et Cosmochimica Acta: Journal of the Geochemical Society and the Meteoritical Society >Sulfur, sulfides, oxides and organic matter aggregated in submarine hydrothermal plumes at 9°50'N East Pacific Rise
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Sulfur, sulfides, oxides and organic matter aggregated in submarine hydrothermal plumes at 9°50'N East Pacific Rise

机译:东太平洋上升9°50'时海底热液羽流中聚集的硫,硫化物,氧化物和有机物

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Deep-sea hydrothermal plume particles are known to sequester seawater trace elements and influence ocean-scale biogeochemical budgets. The relative importance of biotic versus abiotic oxidation-reduction and other particle-forming reaction, however, and the mechanisms of seawater trace element sequestration remain unknown. Suspended particulate material was collected from a non-buoyant hydrothermal plume by in situ filtration at 9°50'N East Pacific Rise during a 3-day, 24 sample, time-series. Twenty-three samples were digested for total elemental analysis. One representative sample was selected for particle-by-particle geochemical analyses including elemental composition by X-ray fluorescence, speciation of Fe, S, and C by 1s X-ray absorption near edge structure spectroscopy, and X-ray diffraction. Consistent with past studies, positive linear correlations were observed for P, V, As, and Cr with Fe in the bulk chemistry. Arsenic was associated with both Fe oxyhydroxides and sulfides but not uniformly distributed among either mineral type. Particle aggregation was common. Aggregates were composed of minerals embedded in an organic matrix; the minerals ranged from <20nm to >10μm in diameter. The speciation of major mineral forming elements (Fe, Mn, S) was complex. Over 20 different minerals were observed, nine of which were either unpredicted by thermodynamic modeling or had no close match in the thermodynamic database. Sulfur-bearing phases consisted of polysulfides (S _6, S _8), and metal sulfides (Fe, Cu, Zn, Mn). Four dominant species, Fe oxyhydroxide, Fe monosulfide, pyrrhotite, and pyrite, accounted for >80% of the Fe present. Particulate Mn was prevalent in both oxidized and reduced minerals. The organic matrix was: (1) always associated with minerals, (2) composed of biomolecules, and (3) rich in S. Possible sources of this S-rich organic matter include entrained near vent biomass and in situ production by S-oxidizing microorganisms. These results indicate that particle aggregation with organic material is prevalent in dispersing hydrothermal plume fluxes, as well as in sinking particulate matter at this site. Particle aggregation and organic coatings can influence the reactivity, transport, and residence time of hydrothermal particles in the water column. Thus a biogeochemical approach is critical to understanding the net effect of hydrothermal fluxes on ocean and sedimentary trace element budgets.
机译:已知深海热液羽流颗粒会隔离海水中的微量元素并影响海洋规模的生物地球化学预算。然而,生物对非生物氧化还原和其他颗粒形成反应的相对重要性以及海水中痕量元素螯合的机理仍然未知。通过在3天,24个样本的时间序列中于9°50'N East Pacific Rise进行原位过滤,从非浮力热液羽流中收集了悬浮的颗粒物质。消化了23个样品以进行总元素分析。选择了一个代表性样品进行逐颗粒地球化学分析,包括通过X射线荧光进行元素组成分析,通过1s X射线近边缘结构光谱吸收对Fe,S和C进行形态分析以及X射线衍射。与以前的研究一致,在本体化学中观察到P,V,As和Cr与Fe呈正线性关系。砷与羟基氧化铁和硫化物有关,但在两种矿物类型中均不均匀分布。颗粒聚集是常见的。骨料由嵌入有机基质中的矿物质组成。矿物的直径范围从<20nm到>10μm。主要矿物形成元素(Fe,Mn,S)的形态很复杂。观察到20多种不同的矿物,其中9种不是通过热力学模型预测的,就是在热力学数据库中没有紧密匹配的矿物。含硫相包括多硫化物(S _6,S _8)和金属硫化物(Fe,Cu,Zn,Mn)。羟基氧化铁,单硫化铁,黄铁矿和黄铁矿这四个主要种类占所含铁的80%以上。氧化和还原矿物质中普遍存在颗粒状锰。有机基质为:(1)始终与矿物质有关,(2)由生物分子组成,以及(3)富含S。这种富含S的有机物的可能来源包括夹带近排放生物质和通过S氧化原位生产微生物。这些结果表明,与有机材料的颗粒聚集在弥散热液羽流中以及在该位置下沉颗粒物方面普遍存在。颗粒聚集和有机涂层会影响水热颗粒在水柱中的反应性,迁移和停留时间。因此,生物地球化学方法对于了解热液通量对海洋和沉积物微量元素收支的净影响至关重要。

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