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The microbially driven formation of siderite in salt marsh sediments. / Lin, Chin Yik; Turchyn, Alexandra V.; Krylov, Alexey; Antler, Gilad.

в: Geobiology, 01.03.2020.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

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Lin, Chin Yik ; Turchyn, Alexandra V. ; Krylov, Alexey ; Antler, Gilad. / The microbially driven formation of siderite in salt marsh sediments. в: Geobiology. 2020.

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@article{d83e0bc602cf41d1bf4a85600e02c87e,
title = "The microbially driven formation of siderite in salt marsh sediments",
abstract = "We employ complementary field and laboratory-based incubation techniques to explore the geochemical environment where siderite concretions are actively forming and growing, including solid-phase analysis of the sediment, concretion, and associated pore fluid chemistry. These recently formed siderite concretions allow us to explore the geochemical processes that lead to the formation of this less common carbonate mineral. We conclude that there are two phases of siderite concretion growth within the sediment, as there are distinct changes in the carbon isotopic composition and mineralogy across the concretions. Incubated sediment samples allow us to explore the stability of siderite over a range of geochemical conditions. Our incubation results suggest that the formation of siderite can be very rapid (about two weeks or within 400 hr) when there is a substantial source of iron, either from microbial iron reduction or from steel material; however, a source of dissolved iron is not enough to induce siderite precipitation. We suggest that sufficient alkalinity is the limiting factor for siderite precipitation during microbial iron reduction while the lack of dissolved iron is the limiting factor for siderite formation if microbial sulfate reduction is the dominant microbial metabolism. We show that siderite can form via heated transformation (at temperature 100°C for 48 hr) of calcite and monohydrocalcite seeds in the presence of dissolved iron. Our transformation experiments suggest that the formation of siderite is promoted when carbonate seeds are present.",
keywords = "calcite, mineralogy, nodule, siderite, sulfate-reducing bacteria, transformation",
author = "Lin, {Chin Yik} and Turchyn, {Alexandra V.} and Alexey Krylov and Gilad Antler",
year = "2020",
month = mar,
day = "1",
doi = "10.1111/gbi.12371",
language = "English",
journal = "Geobiology",
issn = "1472-4677",
publisher = "Wiley-Blackwell",

}

RIS

TY - JOUR

T1 - The microbially driven formation of siderite in salt marsh sediments

AU - Lin, Chin Yik

AU - Turchyn, Alexandra V.

AU - Krylov, Alexey

AU - Antler, Gilad

PY - 2020/3/1

Y1 - 2020/3/1

N2 - We employ complementary field and laboratory-based incubation techniques to explore the geochemical environment where siderite concretions are actively forming and growing, including solid-phase analysis of the sediment, concretion, and associated pore fluid chemistry. These recently formed siderite concretions allow us to explore the geochemical processes that lead to the formation of this less common carbonate mineral. We conclude that there are two phases of siderite concretion growth within the sediment, as there are distinct changes in the carbon isotopic composition and mineralogy across the concretions. Incubated sediment samples allow us to explore the stability of siderite over a range of geochemical conditions. Our incubation results suggest that the formation of siderite can be very rapid (about two weeks or within 400 hr) when there is a substantial source of iron, either from microbial iron reduction or from steel material; however, a source of dissolved iron is not enough to induce siderite precipitation. We suggest that sufficient alkalinity is the limiting factor for siderite precipitation during microbial iron reduction while the lack of dissolved iron is the limiting factor for siderite formation if microbial sulfate reduction is the dominant microbial metabolism. We show that siderite can form via heated transformation (at temperature 100°C for 48 hr) of calcite and monohydrocalcite seeds in the presence of dissolved iron. Our transformation experiments suggest that the formation of siderite is promoted when carbonate seeds are present.

AB - We employ complementary field and laboratory-based incubation techniques to explore the geochemical environment where siderite concretions are actively forming and growing, including solid-phase analysis of the sediment, concretion, and associated pore fluid chemistry. These recently formed siderite concretions allow us to explore the geochemical processes that lead to the formation of this less common carbonate mineral. We conclude that there are two phases of siderite concretion growth within the sediment, as there are distinct changes in the carbon isotopic composition and mineralogy across the concretions. Incubated sediment samples allow us to explore the stability of siderite over a range of geochemical conditions. Our incubation results suggest that the formation of siderite can be very rapid (about two weeks or within 400 hr) when there is a substantial source of iron, either from microbial iron reduction or from steel material; however, a source of dissolved iron is not enough to induce siderite precipitation. We suggest that sufficient alkalinity is the limiting factor for siderite precipitation during microbial iron reduction while the lack of dissolved iron is the limiting factor for siderite formation if microbial sulfate reduction is the dominant microbial metabolism. We show that siderite can form via heated transformation (at temperature 100°C for 48 hr) of calcite and monohydrocalcite seeds in the presence of dissolved iron. Our transformation experiments suggest that the formation of siderite is promoted when carbonate seeds are present.

KW - calcite

KW - mineralogy

KW - nodule

KW - siderite

KW - sulfate-reducing bacteria

KW - transformation

UR - http://www.scopus.com/inward/record.url?scp=85076364072&partnerID=8YFLogxK

U2 - 10.1111/gbi.12371

DO - 10.1111/gbi.12371

M3 - Article

AN - SCOPUS:85076364072

JO - Geobiology

JF - Geobiology

SN - 1472-4677

ER -

ID: 50562310