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Limited reduction of ferrihydrite encrusted by goethite in freshwater sediment

机译:淡水沉积物中针铁矿包裹的水铁矿的还原作用有限

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Many physical and chemical processes control the extent of Fe(III) oxyhydroxide reduction by dissimilatory Fe(III)-reducing bacteria. The surface precipitation of secondary Fe minerals on Fe(III) oxyhydroxides limits the extent of microbial Fe(III) reduction, but this phenomenon has not yet been observed in nature. This paper reports the observation of secondary Fe-mineral (goethite) encrustation on ferrihydrite surface within freshwater sediment up to 10 cm deep. The sediment surface was characterized by the predominance of ferrihydrites with biogenic stalks and sheaths. An Fe(II)-oxidizing bacterium (Gallionellaceae) was detected by 16S rRNA gene analysis at sediment depths of 1 and 2 cm. Fe2+ concentration in the sediment pore water was relatively higher at 2-4 cm depths. The 16S rRNA genes affiliated with dissimilatory Fe(III)-reducing bacteria were detected at 1, 2, and 4 cm depths. The results of the Fe K-edge extended X-ray absorption fine structure (EXAFS) analysis suggested the presence of goethite and siderite at depths below 3 cm. However, the change in the Fe-mineral composition was restricted to sediment depths between 3 and 4 cm, despite the presence of abundant ferrihydrite at depths below 4 cm. An increase in CH4 concentration was observed at deeper than 6 cm. Stable isotopic analysis of CH4 in the pore water indicated that acetoclastic CH4 occurred at depths below 7 cm. Transmission electron microscope observations suggested the presence of goethite and siderite on stalks and sheaths at depths below 3 cm. Results from conversion electron yield EXAFS analysis suggested that goethite dominated at 10 cm depth, thereby indicating that ferrihydrite was encrusted by goethite at this depth. Moreover, the incomplete reduction of ferrihydrite below depths of 4 cm was not due to the lack of organic carbon, but was possibly due to the surface encrustation of goethite on ferrihydrite.
机译:许多物理和化学过程控制着异化还原Fe(III)细菌的氧化氢氧化Fe(III)的程度。 Fe(III)羟基氧化物上次生Fe矿物的表面沉淀限制了微生物Fe(III)的还原程度,但是这种现象在自然界中尚未观察到。本文报道了在深达10 cm的淡水沉积物中,铁矿岩表面上次生铁矿物(针铁矿)结壳的观察结果。沉积物表面的特征是亚铁酸盐中含有大量生物茎和鞘。通过16S rRNA基因分析在1和2 cm的沉积物深度检测到Fe(II)氧化细菌(Gallionellaceae)。沉积物孔隙水中的Fe2 +浓度在2-4 cm深度处相对较高。在1、2和4 cm深度检测到与异化Fe(III)还原细菌相关的16S rRNA基因。 Fe K边缘扩展X射线吸收精细结构(EXAFS)分析的结果表明,深度低于3 cm时存在针铁矿和菱铁矿。然而,尽管在4 cm以下的深度存在大量的水铁矿,但Fe矿物成分的变化仅限于3至4 cm的沉积物深度。在深于6 cm处观察到CH4浓度增加。孔隙水中CH4的同位素分析表明,碎裂CH4发生在7 cm以下的深度。透射电子显微镜观察表明,在低于3 cm的深度的茎和鞘中存在针铁矿和菱铁矿。转换电子产率EXAFS分析的结果表明,针铁矿在10 cm的深度占主导地位,从而表明在该深度,针铁矿包裹了水铁矿。此外,在4 cm深度以下,水铁矿的还原不完全不是由于缺少有机碳,而是由于针铁矿在水铁矿上的表面结壳所致。

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