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Biogeochemical reappraisal of the freshwater–seawater mixing-zone diagenetic model

The result's identifiers

  • Result code in IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F60077344%3A_____%2F21%3A00545490" target="_blank" >RIV/60077344:_____/21:00545490 - isvavai.cz</a>

  • Alternative codes found

    RIV/00025798:_____/21:00000049

  • Result on the web

    <a href="https://onlinelibrary.wiley.com/doi/10.1111/sed.12849" target="_blank" >https://onlinelibrary.wiley.com/doi/10.1111/sed.12849</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.1111/sed.12849" target="_blank" >10.1111/sed.12849</a>

Alternative languages

  • Result language

    angličtina

  • Original language name

    Biogeochemical reappraisal of the freshwater–seawater mixing-zone diagenetic model

  • Original language description

    First proposed nearly half a century ago, the mixing-zone model of dolomitization enjoyed a brief stay in the limelight before falling out of favour. Despite extended past criticism, arguments that build on its current validity are presented and discussed. The coastal mixing zone can be seen as an aquifer system exhibiting marked physicochemical gradients, reflective of the admixture of low salinity freshwater and seawater sources with variable redox potentials. This perspective requires a more holistic look at the mixing zone, not only as a gradient of major element concentrations, but also as the locus of enhanced subsurface redox sensitive reactions that occur at the pore-space scale within a moveable diagenetic front. Combined genomic and isotopic data indicate that an active subsurface biosphere thrives in the mixing zone. This could facilitate Mg2+ dehydration, generate alkalinity, consume protons and mobilize potentially catalyzing ions (i.e. Mn and Zn), which are all low temperature factors thought to promote dolomite formation from soluble precursors. In the updated model, the advective mix of fluids with contrasting composition modulate a range of biogeochemically induced mineral dissolution and reprecipitation reactions. Biotic and abiotic interactions between these fluids affect carbonate equilibrium and result in dissolution of soluble aragonitic and calcitic phases, while dolomite precipitates (as cement) and neomorphic replacement. The secondary dolomite often exhibits compositional heterogeneity and contentious δ18O signatures indicative of re-equilibration. The role of manganese, zinc, intermediate sulphur species and ammonia are far from being fully understood, nor is their fingerprint in ancient deposits. Application of in situ spectroscopic imaging techniques, clumped and metal isotope analyses, as well as a more extended use of traditional approaches, such as sulphur isotopes, are poised to open many opportunities to further explore the biogeochemistry of this diagenetic environment and how it relates to platform dolomitization.

  • 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

    10505 - Geology

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

    P - Projekt vyzkumu a vyvoje financovany z verejnych zdroju (s odkazem do CEP)

Others

  • Publication year

    2021

  • Confidentiality

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

Data specific for result type

  • Name of the periodical

    Sedimentology

  • ISSN

    0037-0746

  • e-ISSN

    1365-3091

  • Volume of the periodical

    68

  • Issue of the periodical within the volume

    5

  • Country of publishing house

    GB - UNITED KINGDOM

  • Number of pages

    34

  • Pages from-to

    1797-1830

  • UT code for WoS article

    000637480700001

  • EID of the result in the Scopus database

    2-s2.0-85103905527