热带河口潮汐尺度的溶解无机碳和颗粒有机碳动力学

IF 3 3区 地球科学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Mohammad Atif Khan , Sanjeev Kumar , Rajdeep Roy , Satya Prakash , Aneesh A. Lotliker , Sanjiba Kumar Baliarsingh
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引用次数: 0

摘要

对全球河口的溶解无机碳(DIC)和颗粒有机碳(POC)动力学进行了月度、季节和年度时间 尺度的广泛研究,重点是它们的浓度和向沿岸海洋的输出通量。然而,鉴于河口的动态性质,潮汐和昼夜周期对 DIC 和 POC 动态调节过程的影响仍不明显。为了破译潮汐尺度下的生物地球化学过程,研究人员在印度东海岸的热带河口马哈纳迪河口连续九天(2019 年 10 月 14-23 日)的涨潮和退潮时测量了不同盐度梯度的 DIC 和 POC 浓度及其碳和氮同位素组成。不同盐度梯度的 DIC、POC 及其同位素组成呈现出截然不同的差异。这表明由于水位波动和河口混合区的混合强度,春-夏潮汐周期产生了影响。线性最小二乘回归模型表明,碳酸盐和/或硅酸盐风化产生的生物源二氧化碳可能是河口淡水区域的 DIC 来源。观测到的 DIC 浓度和 δ13CDIC 与保守混合值的偏差表明,混合区的 DIC 来源特征发生了明显变化。为确定影响 DIC 动态的可能生物地球化学过程,采用了基于过程的模型方法,结果表明,退潮时的方解石溶解和涨潮时的方解石沉淀是混合区的主要过程。此外,还观察到多个生物地球化学过程同时调节 DIC 动态。混合区的 POC 池主要受涨潮和退潮期间通过快速再矿化去除 POC 的影响。图表还显示,混合区和盐水区的 POC 受降解等过程的影响较大,而河口淡水区的 POC 仅受轻微影响。δ13CPOC以及POM的C/N比表明,C3植物和/或其衍生土壤是淡水中POM的主要来源,而在混合区和盐碱地,河流POM和海洋浮游植物的贡献率分别较高。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Tidal scale dissolved inorganic and particulate organic carbon dynamics in a tropical estuary

Dissolved inorganic carbon (DIC) and particulate organic carbon (POC) dynamics in the world's estuaries have been studied extensively at monthly, seasonal, and annual time scales with particular focus on their concentrations and export fluxes to the coastal oceans. However, given the dynamic nature of the estuaries, the effect of tidal and diel cycles on the processes modulating DIC and POC dynamics remains obscure. To decipher the biogeochemical processes at tidal scale, DIC and POC concentrations and their carbon and nitrogen isotopic compositions were measured across the salinity gradient at every high and low tide for nine consecutive days (14–23 October 2019) in the Mahanadi estuary, a tropical estuary at the east coast of India. Showing contrasting differences across salinity gradient in DIC, POC and their isotopic compositions, DIC and POC were significantly different during high and low tide in the mixing zone only during spring duration. This showed the effect of spring-neap tidal cycle owing to water level fluctuations and mixing intensity in the estuarine mixing zone. Linear least-squares regression models indicated carbonate and/or silicate weathering by biogenic CO2 to be the probable DIC source in the freshwater region of the estuary. Deviations of observed DIC concentrations and δ13CDIC from the conservative mixing values suggested pronounced alteration of DIC source signature in the mixing zone. A process-based model approach aimed at delineating possible biogeochemical processes affecting DIC dynamics indicated calcite dissolution during low tide and calcite precipitation during high tide to be dominant processes in the mixing zone. Additionally, signatures of more than one simultaneous biogeochemical process modulating the DIC dynamics were also observed. POC pool in the mixing zone was largely influenced by its removal through rapid remineralization during both high and low tides. Graphical plots also showed that POC in the mixing zone and at the saline location was significantly affected by processes such as degradation, whereas it was only slightly affected in the freshwater region of the estuary. δ13CPOC, along with the C/N ratio of POM, indicated that C3 plants and/or their derived soil were the major source of POM in the freshwater, whereas the higher contribution of riverine POM and marine phytoplankton was observed in the mixing zone and saline location, respectively.

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来源期刊
Marine Chemistry
Marine Chemistry 化学-海洋学
CiteScore
6.00
自引率
3.30%
发文量
70
审稿时长
4.5 months
期刊介绍: Marine Chemistry is an international medium for the publication of original studies and occasional reviews in the field of chemistry in the marine environment, with emphasis on the dynamic approach. The journal endeavours to cover all aspects, from chemical processes to theoretical and experimental work, and, by providing a central channel of communication, to speed the flow of information in this relatively new and rapidly expanding discipline.
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