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首页> 外文期刊>Clays and clay minerals >BIOGEOCHEMICAL AND ENVIRONMENTAL FACTORS IN Fe BIOMINERALIZATION: MAGNETITE AND SIDERITE FORMATION
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BIOGEOCHEMICAL AND ENVIRONMENTAL FACTORS IN Fe BIOMINERALIZATION: MAGNETITE AND SIDERITE FORMATION

机译:铁矿化中的生物地球化学和环境因素:磁铁矿和绢云母形成

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The formation of siderite and magnetite by Fe(Ⅲ)-reducing bacteria may play an important role in C and Fe geochemistry in subsurface and ocean sediments. The objective of this study was to identify environmental factors that control the formation of siderite (FeCO_3) and magnetite (Fe_3O_4) by Fe(Ⅲ)-rcducing bacteria. Psychrotolerant (<20℃), mesophilic (20-35℃) and thermophilic (>45℃) Fe(Ⅲ)-reducing bacteria were used to examine the reduction of a poorly crystalline iron oxide, akaganeitc (β-FeOOH), without a soluble electron shuttle, anthraquinone disulfuonate (AQDS), in the presence of N_2, N_2-CO_2(80:20, V:V), H_2 and H_2-CO_2 (80:20, V:V) headspace gases as well as in HCO_3~--buffered medium (30-210 mM) under a N_2 atmosphere. Iron biomineralization was also examined under different growth conditions such as salinity, pH, incubation time, incubation temperature and electron donors. Magnetite formation was dominant under a N_2 and a H_2 atmosphere. Siderite formation was dominant under a H_2-CO_2 atmosphere. A mixture of magnetite and siderite was formed in the presence of a N_2-CO_2 headspace. Akaganeite was reduced and transformed to siderite and magnetite in a HCO_3~--buffered medium (>120 mM) with lactate as an electron donor in the presence of a N_2 atmosphere. Biogeochemical and environmental factors controlling the phases of the secondary mineral suite include medium pH, salinity, electron donors, atmospheric composition and incubation time. These results indicate that microbial Fe(Ⅲ) reduction may play an important role in Fe and C biogeochemistry as well as C sequestration in natural environments.
机译:还原铁(Ⅲ)的细菌形成菱铁矿和磁铁矿可能在地下和海洋沉积物中的碳和铁地球化学中起重要作用。这项研究的目的是确定环境因素,这些环境因素控制着引起Fe(Ⅲ)的细菌形成菱铁矿(FeCO_3)和磁铁矿(Fe_3O_4)的形成。用抗精神病药(<20℃),嗜温(20-35℃)和嗜热(> 45℃)还原Fe(Ⅲ)的细菌检查结晶度较弱的氧化铁,akaganeitc(β-FeOOH)的还原。 N_2,N_2-CO_2(80:20,V:V),H_2和H_2-CO_2(80:20,V:V)顶空气体以及HCO_3存在下的可溶性电子穿梭蒽醌二磺酸盐(AQDS)在N_2气氛下,缓冲液(30-210 mM)。还在不同的生长条件下(例如盐度,pH,孵育时间,孵育温度和电子供体)检查了铁的生物矿化作用。在N_2和H_2气氛下,磁铁矿占主导地位。在H_2-CO_2气氛下,菱铁矿的形成占主导地位。在N_2-CO_2顶部空间的存在下形成磁铁矿和菱铁矿的混合物。在N_2气氛下,以乳酸作为电子给体的HCO_3缓冲介质(> 120 mM)中,赤铁矿被还原并转化为菱铁矿和磁铁矿。控制次生矿物质相的生物地球化学和环境因素包括中等pH值,盐度,电子给体,大气成分和孵育时间。这些结果表明,微生物对Fe(Ⅲ)的还原可能在Fe和C的生物地球化学以及自然环境中的C螯合中起重要作用。

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