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首页> 外文期刊>Organic Geochemistry: A Publication of the International Association of Geochemistry and Cosmochemistry >Distribution and biogeochemistry of sedimentary humic substances in the St. Lawrence Estuary and the Saguenay Fjord, Québec
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Distribution and biogeochemistry of sedimentary humic substances in the St. Lawrence Estuary and the Saguenay Fjord, Québec

机译:魁北克圣劳伦斯河口和萨格奈峡湾中的腐殖质沉积物分布和生物地球化学

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The concentrations of sedimentary humic substances (HS) were measured in the St. Lawrence marine system, Québec (Canada), including the Saguenay Fjord. Concentration ranges for humin, humic acids and fulvic acids were 7–49, 1–19, and 0.5–6 mg per gram of sediment (dry weight), respectively. HS always represented the dominant component of sediment organic matter (SOM) (i.e., 52–100%) for which humin, humic acids, and fulvic acids accounted for 38–88%, 4–28%, and 2–14%, respectively. These results indicate that most HS and an important part of SOM were associated with the mineral matrix and thus defined as humin. HS concentrations varied slightly by site location and depth but major changes in concentration in the fjord were caused by episodic events such as floods and landslides. In the fjord, sedimentary HS were mostly terrigenous and molecules such as lignin likely contributed to the high proportions of HS. In the St. Lawrence Estuary, an important input of marine particulate organic matter and favorable conditions for its degradation seem to have promoted the mineralization of the labile SOM before its burial. The less labile SOM was buried in sediments where humification and stabilization appeared to occur. Such processes could explain the lower SOM concentrations but greater humin proportions with increasing distance downstream and sediment depth. Estimations based on HS profiles suggest that ~25% of the surface SOM will be preserved in deeper layers (i.e., >1 m), principally in the form of humin. Sorption of organic matter onto mineral surfaces might have contributed to SOM preservation and humin stabilization in sediments. DRIFT spectroscopy suggests that carboxylate groups may mediate this sorption.
机译:在魁北克(加拿大)的圣劳伦斯海洋系统(包括萨格奈峡湾)中测量了腐殖质(HS)的浓度。腐殖质,腐殖酸和黄腐酸的浓度范围分别为每克沉积物(干重)7–49、1–19和0.5–6 mg。 HS始终代表沉积物有机质(SOM)的主要成分(即52-100%),其中腐殖质,腐殖酸和黄腐酸分别占38-88%,4-28%和2-14% 。这些结果表明大多数HS和SOM的重要部分与矿物基质有关,因此被定义为腐殖质。 HS浓度随地点和深度的不同而略有不同,但峡湾浓度的主要变化是由洪水和滑坡等突发事件引起的。在峡湾中,沉积的HS主要是陆源的,而诸如木质素的分子可能是高比例的HS。在圣劳伦斯河口,海洋颗粒有机物的大量投入及其降解的有利条件似乎促进了不稳定的SOM埋藏前的矿化作用。不太稳定的SOM被埋在似乎发生腐化和稳定作用的沉积物中。这样的过程可以解释出较低的SOM浓度,但是随着下游距离和沉积物深度的增加,腐殖质的比例也更高。根据HS剖面的估算表明,约25%的表面SOM将保留在更深的层(即> 1 m)中,主要以腐殖质形式存在。将有机物吸附到矿物表面上可能有助于SOM的保存和沉积物中人胶的稳定。 DRIFT光谱表明,羧酸盐基团可以介导这种吸附。

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