首页> 外文期刊>The Science of the Total Environment >In-situ, high-resolution evidence from water-sediment interface for significant role of iron bound phosphorus in eutrophic lake
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In-situ, high-resolution evidence from water-sediment interface for significant role of iron bound phosphorus in eutrophic lake

机译:水-沉积物界面的原位高分辨率证据证明了铁结合磷在富营养化湖泊中的重要作用

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Potential release of phosphorus (P) bound to iron (Fe) is critical because of the aggravating effects on P load in aquatic ecosystems. However, the process is largely unknown due to the absence of in-situ high-resolution evidence. Dissolved oxygen (DO), ferrous ion (Fe~(2+)), and dissolved reactive phosphate (DRP) in interstitial water of sediment columns from a eutrophic shallow lake were measured using the novel colorimetric planar optode imaging method and ZrO-Chelex DGT technology during controlled experimental episodes. The solid Fe and P fractions in sediments were also simultaneously evaluated by employing sequential extraction procedure and spectra scanning analysis including SEM-EDS and ~(57)Fe-Moessbauer spectroscopy. The results demonstrated that the DO penetration depths were accordingly regulated with time, the depths depended on the oxygen supply patterns, and oxygen depletion occurred at anaerobic intervals. Considerable increases of concentrations and diffusion of Fe~(2+) and DRP in interstitial water upward from the deep layer into the overlying water were mirrored by decreased concentrations of solid Fe bound P and mineral phase Fe(II) during an anaerobic episode. This confirmed that the re-dissolution of solid Fe bound P pools is the most important source of labile P. and aggravates the P budget in lake water via anaerobic intervals. The reduction-precipitation mechanism of Fe bound P during different oxidation scenarios indicated that the Fe bound P in sediments can act as intermediates between Po and Ca bound P, and result in the permanent burying of authigenic Ca bound P. Significantly positive correlations (R~2 ≥ 0.7783. n = 74) between labile Fe~(2+) and DRP on both redox conditions also provided explicit evidence for the critical role of redox controlling Fe in labile P cycling at the lacustrine sediment-water interface. These findings provide improved insight for potential controlling effort of Fe coupled P to labile P depending on the oxygen supply in shallow-water hypereutrophic lakes.
机译:由于对水生生态系统中磷负荷的加剧影响,与铁(Fe)结合的磷(P)的潜在释放至关重要。然而,由于缺乏原位高分辨率证据,该过程在很大程度上是未知的。利用新型比色平面光电成像方法和ZrO-Chelex DGT技术对富营养化浅水湖泊沉积物柱间质水中的溶解氧(DO),亚铁离子(Fe〜(2+))和溶解性磷酸盐(DRP)进行了测量。技术可控制的实验期间。还通过采用顺序萃取程序和包括SEM-EDS和〜(57)Fe-Moessbauer光谱在内的光谱扫描分析,同时评估了沉积物中的固体Fe和P分数。结果表明,DO的渗透深度随时间而变化,深度取决于供氧方式,并且厌氧时间间隔内会发生耗氧。在厌氧过程中,固结Fe和矿物相Fe(II)的浓度降低反映了间隙水中Fe〜(2+)和DRP从深层向上进入上覆水中的浓度和扩散的显着增加。这证实了固结铁结合的磷库的再溶解是不稳定磷的最重要来源,并且通过厌氧间隔加剧了湖水中磷的预算。 Fe结合P在不同氧化情况下的还原沉淀机制表明,沉积物中的Fe结合P可以作为Po和Ca结合P之间的中间物,并导致自生Ca结合P的永久埋藏。显着正相关(R〜在两种氧化还原条件下,不稳定的Fe〜(2+)和DRP之间的2≥0.7783。n = 74)也提供了明确的证据,说明氧化还原控制Fe在湖沉积物-水界面的不稳定P循环中的关键作用。这些发现为浅水富营养化湖泊中的氧气供应提供了更好的洞察力,帮助人们将铁耦合的磷与不稳定的磷进行潜在的控制。

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