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Redox dynamics and metal cycling in the carbonate-buffered sediment–water interface of the ferruginous and sulfatic Lake Medard, Czech Republic

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F25%3A00638660" target="_blank" >RIV/60077344:_____/25:00638660 - isvavai.cz</a>

  • Alternative codes found

    RIV/60076658:12310/25:43910785 RIV/00025798:_____/25:10169514

  • Result on the web

    <a href="https://pubs.geoscienceworld.org/sepm/jsedres/article-abstract/95/4/707/653835/Redox-dynamics-and-metal-cycling-in-the-carbonate?redirectedFrom=fulltext" target="_blank" >https://pubs.geoscienceworld.org/sepm/jsedres/article-abstract/95/4/707/653835/Redox-dynamics-and-metal-cycling-in-the-carbonate?redirectedFrom=fulltext</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.2110/jsr.2024.155" target="_blank" >10.2110/jsr.2024.155</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Redox dynamics and metal cycling in the carbonate-buffered sediment–water interface of the ferruginous and sulfatic Lake Medard, Czech Republic

  • Original language description

    Lake Medard (LM), a post-mining lake in the Czech Republic with stratified, sulfate- and iron-rich bottom waters, serves as a natural laboratory to study sediment–water-interface (SWI) dynamics where steep aqueous redox gradients are present. This study investigates the interplay of redox conditions, microbial activity, and sedimentary processes, revealing that short-term Eh fluctuations (80–100 mV) in the bottom water significantly mobilize rare earth elements (REE) and influence the partitioning of other redox-sensitive elements such as vanadium (V) and arsenic (As) from reactive iron (Fe)- and manganese (Mn)-oxyhydroxides during early diagenesis. While carbonate phases like siderite primarily retain their REE signatures, they can incorporate REE released during these redox shifts. Spectroscopic analyses confirms the presence of FeOOH polymorphs (goethite and lepidocrocite) in organo-mineral aggregates in the upper sediments. Sequential extractions shows that under stronger reducing conditions (Eh ≈ –190 mV), As predominantly associates with carbonates, shifting to Fe(III)-oxyhydroxides at higher Eh (≈ –80 mV). Isotope analyses (d13C) indicate that the bulk sediment carbonate is detrital, sourced from Miocene strata. Authigenic pyrite in LM sediments exhibits d34Spy values (–35.1 to –23.0%), reflecting microbial sulfate reduction. However, the accumulation of the byproduct sulfide, and thus pyrite stabilization, is limited by the low availability of labile organic substrates and the reoxidation of sulfide by Fe(III)-oxyhydroxides. These findings highlight the sensitivity of geochemical signals in sediments to subtle redox shifts and improve our interpretation of ancient deposits formed under dynamic water column redox conditions.

  • Czech name

  • Czech description

Classification

  • Type

    J<sub>imp</sub> - Article in a specialist periodical, which is included in the Web of Science database

  • CEP classification

  • OECD FORD branch

    10511 - Environmental sciences (social aspects to be 5.7)

Result continuities

  • Project

    <a href="/en/project/GJ19-15096Y" target="_blank" >GJ19-15096Y: Microbially induced iron, nitrogen and phosphorus co-recycling and transient decoupling in aqueous ferruginous ecosystems</a><br>

  • Continuities

    I - Institucionalni podpora na dlouhodoby koncepcni rozvoj vyzkumne organizace

Others

  • Publication year

    2025

  • Confidentiality

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Data specific for result type

  • Name of the periodical

    Journal of Sedimentary Research

  • ISSN

    1527-1404

  • e-ISSN

    1938-3681

  • Volume of the periodical

    95

  • Issue of the periodical within the volume

    4

  • Country of publishing house

    US - UNITED STATES

  • Number of pages

    16

  • Pages from-to

    707-722

  • UT code for WoS article

    001666225000002

  • EID of the result in the Scopus database

    2-s2.0-105013135169