Aggregation and Dispersion Behaviours of Riverine Trace Metals (Fe, Al, V, Mn, Ni, and Zn) and Organic Matter in Freshwater and Estuarine Conditions: A case study in Shira and Midori Rivers, Kumamoto, Japan

IF 1.7 4区 地球科学 Q3 GEOCHEMISTRY & GEOPHYSICS Aquatic Geochemistry Pub Date : 2022-11-27 DOI:10.1007/s10498-022-09408-7
Hiroaki Ito, Shinya Tsurumaki, Takehide Hama, Kei Ishida, Tsugihiro Watanabe, Luong van Duc, Yasunori Kawagoshi
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Abstract

The aggregation and dispersion of metals and organic matter are an important morphological alteration process for their transportation and bioavailability in coastal areas. However, variable mixing behaviours can be observed for some substances (e.g. Mn and Cu) due to the variable interaction systems in natural systems. In this study, riverine freshwater in the Shira and Midori rivers, Kumamoto, Japan, was mixed with artificial seawater to investigate the aggregation and dispersion behaviours of trace metals (i.e. Fe, Al, Mn, Zn, Cu, V, and Ni) and organic matter. In particular, their interactions were examined with differentiating the fast and slow transformations and considering the effects of suspended substances. Comparisons of sequential processes, including seawater mixing, decantation, centrifugation, and multiple filtrations, illustrated the aggregation and dispersion characteristics of the metals and organic matter as follows. A strong aggregating nature was evident for Fe in estuarine systems. In addition, the slow aggregation of Fe was accelerated by river-borne suspended substances. Small Fe (oxy)hydroxide particles were the major forms of dissolved Fe in both freshwater and estuarine systems and were partly associated with the other metals. In contrast, Zn and Ni were characterised by strong dispersion properties, although it can resorb onto suspended substances in estuarine systems. Synchronous behaviours with Zn and Ni were observed for V, Cu, and organic matter in the Midori River. The adsorption of Mn onto suspended substances was evident in the freshwater systems instead of the estuarine systems. Meanwhile, the behaviour of Mn is known to be dependent on its abundance in suspended forms, its redox state, and the influence of Fe. V and Cu, which are non-conservative in nature, were affected by other metals such as Fe, Zn, and Ni. Al, whose behaviour is largely dependent on the target estuary, which was also affected by other metals. Slow aggregation of organic matter was induced by suspended substances which were produced by fast transformation. In addition, evident interactions between suspended and dissolved substances were observed with the behaviours of Fe, Zn, Ni, and organic matter, indicating that the deposition and dispersion at the early stage of estuarine mixing can influence the subsequent slow transformation in real environments.

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河流微量金属(铁、铝、钒、锰、镍和锌)和有机物在淡水和河口条件下的聚集和分散行为:日本熊本县白河和绿河的案例研究
金属和有机物的聚集和分散是它们在沿岸地区迁移和生物利用的重要形态变化过程。然而,由于自然系统中的相互作用系统多变,一些物质(如锰和铜)的混合行为会出现变 化。在这项研究中,将日本熊本白河和绿河的河水淡水与人工海水混合,研究了痕量金 属(即铁、铝、锰、锌、铜、钒和镍)和有机物的聚集和分散行为。特别是,研究了它们之间的相互作用,区分了快速和慢速转化,并考虑了悬浮物质的影响。通过对海水混合、倾析、离心和多次过滤等连续过程的比较,可以看出金属和有机物的聚集和分散特性如下。在河口系统中,铁的聚集性很强。此外,河流中的悬浮物质加速了铁的缓慢聚集。在淡水和河口系统中,小的(氧)氢氧化铁颗粒是溶解铁的主要形式,并与其他金属有部分关联。与此相反,锌和镍具有很强的分散特性,尽管在河口系统中它会吸附在悬浮物质上。在 Midori 河中观察到 V、Cu 和有机物与 Zn 和 Ni 的同步行为。锰对悬浮物质的吸附作用在淡水系统中明显,而在河口系统中则不明显。同时,众所周知,锰的行为取决于其在悬浮物中的丰度、氧化还原状态以及铁的影响。V 和 Cu 的性质是非守恒的,它们受到其他金属(如 Fe、Zn 和 Ni)的影响。铝的行为在很大程度上取决于目标河口,它也受到其他金属的影响。有机物的缓慢聚集是由快速转化产生的悬浮物质引起的。此外,在铁、锌、镍和有机物的行为中,还观察到悬浮物质和溶解物质之间明显的相互作用,这表明河口混合初期的沉积和分散会影响实际环境中随后的缓慢转化。
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来源期刊
Aquatic Geochemistry
Aquatic Geochemistry 地学-地球化学与地球物理
CiteScore
4.30
自引率
0.00%
发文量
6
审稿时长
1 months
期刊介绍: We publish original studies relating to the geochemistry of natural waters and their interactions with rocks and minerals under near Earth-surface conditions. Coverage includes theoretical, experimental, and modeling papers dealing with this subject area, as well as papers presenting observations of natural systems that stress major processes. The journal also presents `letter''-type papers for rapid publication and a limited number of review-type papers on topics of particularly broad interest or current major controversy.
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