Simon David Herzog, Viktoriia Mekelesh, Margarida Soares, Ulf Olsson, Per Persson, Emma Sofia Kritzberg
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The results show a decrease in Fe and OM concentrations in the water column with increasing distance from the inlet. Winter sampling revealed a shift in Fe speciation from dominance of organically complexed Fe to an increase in Fe(oxy)hydroxide, accompanied by a loss of aromatic and carboxylate function of OM. Summer sampling revealed no significant changes along the gradient, with Fe(oxy)hydroxide and carbohydrates dominating the water phase. Interestingly, settling particles and surface sediments were dominated by Fe(oxy)hydroxides and aliphatic OM. We propose that phototransformation may be an important process that influences the interaction between Fe and OM and, as a consequence, their fate along the spatial gradient. Our study suggests a photochemically induced loss of carboxylate groups, reflected by an increased carbohydrate-to-carboxylate ratio along the gradient, particularly in winter, and generally lower levels during summer. Loss of carboxylate function promotes the formation of Fe(oxy)hydroxides, which in turn, facilitates the aggregation and sinking of OM, particularly aliphatic components. These insights contribute to a broader understanding of carbon cycling and storage in lakes. Future studies should assess the significance of photochemical processes to OM burial and it how may change given trends in Fe and OM in northern regions.</p>","PeriodicalId":8901,"journal":{"name":"Biogeochemistry","volume":"208 1","pages":""},"PeriodicalIF":3.9000,"publicationDate":"2024-10-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Iron as a precursor of aggregation and vector of organic carbon to sediments in a boreal lake\",\"authors\":\"Simon David Herzog, Viktoriia Mekelesh, Margarida Soares, Ulf Olsson, Per Persson, Emma Sofia Kritzberg\",\"doi\":\"10.1007/s10533-024-01184-6\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>While organic matter (OM) interactions in the water column prevent iron (Fe) precipitation and sedimentation, Fe also acts as a precursor of aggregation and a vector of OM to sediments. 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Interestingly, settling particles and surface sediments were dominated by Fe(oxy)hydroxides and aliphatic OM. We propose that phototransformation may be an important process that influences the interaction between Fe and OM and, as a consequence, their fate along the spatial gradient. Our study suggests a photochemically induced loss of carboxylate groups, reflected by an increased carbohydrate-to-carboxylate ratio along the gradient, particularly in winter, and generally lower levels during summer. Loss of carboxylate function promotes the formation of Fe(oxy)hydroxides, which in turn, facilitates the aggregation and sinking of OM, particularly aliphatic components. These insights contribute to a broader understanding of carbon cycling and storage in lakes. 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引用次数: 0
摘要
虽然水体中有机物(OM)的相互作用会阻止铁(Fe)的沉淀和沉积,但铁也是聚集的前体和将 OM 带入沉积物的载体。本研究旨在描述铁-OM 相互作用的特征,以了解铁在促进 OM 聚集和迁移方面的作用。在一个北方湖泊中,从入海口开始到离岸,沿梯度从水、沉降物和沉积物中收集了铁和 OM 样品。采用 X 射线吸收光谱(XAS)测定了铁的种类,并采用漫反射红外傅立叶变换光谱(DRIFT IR)和核磁共振光谱(NMR)评估了 OM 的化学成分。结果表明,随着与进水口距离的增加,水体中铁和 OM 的浓度也在下降。冬季取样显示,铁的种类从有机络合铁为主转变为氢氧化铁增加,同时 OM 的芳香族和羧酸盐功能丧失。夏季取样显示,沿梯度方向无明显变化,氢氧化铁和碳水化合物在水相中占主导地位。有趣的是,沉降颗粒和表层沉积物主要是氢氧化铁和脂肪族 OM。我们认为,光转化可能是影响铁和 OM 之间相互作用的一个重要过程,从而影响它们在空间梯度上的归宿。我们的研究表明,光化学诱导了羧酸基的丧失,这反映在梯度上碳水化合物与羧酸基的比率增加,尤其是在冬季,而夏季的比率普遍较低。羧基功能的丧失会促进铁(氧)氢氧化物的形成,这反过来又会促进 OM(尤其是脂肪族成分)的聚集和下沉。这些见解有助于更广泛地了解湖泊中的碳循环和碳储存。未来的研究应评估光化学过程对 OM 埋藏的重要性,以及北方地区铁和 OM 的变化趋势。
Iron as a precursor of aggregation and vector of organic carbon to sediments in a boreal lake
While organic matter (OM) interactions in the water column prevent iron (Fe) precipitation and sedimentation, Fe also acts as a precursor of aggregation and a vector of OM to sediments. This study aims to characterize Fe–OM interactions to understand the role of Fe in promoting aggregation and transport of OM. Samples of Fe and OM were collected from water, settling material, and sediment along a gradient starting from the inlet and continuing offshore within a boreal lake. Fe speciation was determined using X-ray absorption spectroscopy (XAS), and the chemical composition of OM was assessed using Diffuse reflectance infrared Fourier transform spectroscopy (DRIFT IR) and Nuclear magnetic resonance spectroscopy (NMR). The results show a decrease in Fe and OM concentrations in the water column with increasing distance from the inlet. Winter sampling revealed a shift in Fe speciation from dominance of organically complexed Fe to an increase in Fe(oxy)hydroxide, accompanied by a loss of aromatic and carboxylate function of OM. Summer sampling revealed no significant changes along the gradient, with Fe(oxy)hydroxide and carbohydrates dominating the water phase. Interestingly, settling particles and surface sediments were dominated by Fe(oxy)hydroxides and aliphatic OM. We propose that phototransformation may be an important process that influences the interaction between Fe and OM and, as a consequence, their fate along the spatial gradient. Our study suggests a photochemically induced loss of carboxylate groups, reflected by an increased carbohydrate-to-carboxylate ratio along the gradient, particularly in winter, and generally lower levels during summer. Loss of carboxylate function promotes the formation of Fe(oxy)hydroxides, which in turn, facilitates the aggregation and sinking of OM, particularly aliphatic components. These insights contribute to a broader understanding of carbon cycling and storage in lakes. Future studies should assess the significance of photochemical processes to OM burial and it how may change given trends in Fe and OM in northern regions.
期刊介绍:
Biogeochemistry publishes original and synthetic papers dealing with biotic controls on the chemistry of the environment, or with the geochemical control of the structure and function of ecosystems. Cycles are considered, either of individual elements or of specific classes of natural or anthropogenic compounds in ecosystems. Particular emphasis is given to coupled interactions of element cycles. The journal spans from the molecular to global scales to elucidate the mechanisms driving patterns in biogeochemical cycles through space and time. Studies on both natural and artificial ecosystems are published when they contribute to a general understanding of biogeochemistry.