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Sulphur, oxygen and strontium isotope compositions of Middle Miocene (Badenian) calcium sulphates from the Carpathian Foredeep, Poland: Palaeoenvironmental implications

dc.contributor.authorKasprzyk, Alicja
dc.contributor.authorPueyo, Juan J.
dc.contributor.authorHałas, Stanisław
dc.contributor.authorFuenlabrada Pérez, José Manuel
dc.date.accessioned2024-05-20T18:23:58Z
dc.date.available2024-05-20T18:23:58Z
dc.date.issued2007
dc.description.abstractSulphur, oxygen and strontium isotope compositions have been measured in sulphate (gypsum and anhydrite) samples from the Badenian evaporite complex in the Carpathian Foredeep Basin (Poland) to determine the origin of brines from which these sulphates were formed. Studied samples display the δ values from +22.68 to +24.91‰ CDT for sulphur (ten samples) and from +12.26 to + 13.63‰ SMOW for oxygen (ten samples), and 87Sr/86Sr ratios from 0.708915 to 0.716329 (six samples). Most samples show isotopic values (both δ 34S and 87Sr/86Sr) higher than contemporaneous (Badenian) seawater, and thus suggest that these sulphates were formed (i) from brines with a significant component of non-marine waters, (ii) in a restricted system, where an important role was played by meteoric water inputs as well as by bacterial sulphate reduction. The results of this study show clear differences in the isotopic signatures between sedimentary (gypsum) and diagenetic (anhydrite) lithofacies. While sedimentary gypsum displays sulphur, oxygen and strontium isotope ratios close to contemporaneous (Badenian) seawater, diagenetic anhydrite values are largely elevated. The higher isotopic values (δ34S, δ18O and 87Sr/86Sr) for anhydrite when compared to gypsum are interpreted as reflecting different hydrological provenances of sulphate in the Badenian basin. Gypsum was formed from brines marine in origin that were subject to an important inflow of continental waters and a local bacterial sulphate reduction in a restricted, and therefore sulphate-limited basin, which is consistent with earlier interpretations based on sedimentological and geochemical studies. Our study shows that brines from which anhydrite was formed had a highly-radiogenic non-marine (riverine, groundwater) strontium component, which is a new contribution to the knowledge on the Badenian sulphate formation. The results reflect a lateral compositional evolution of parent waters during sulphate deposition and diagenesis in the Carpathian Foredeep Basin.
dc.description.departmentDepto. de Mineralogía y Petrología
dc.description.facultyFac. de Ciencias Geológicas
dc.description.refereedTRUE
dc.description.sponsorshipPolish Committee for Scientific Research
dc.description.statuspub
dc.identifier.citationKasprzyk A., Pueyo J. J., Hałas S. and Fuenlabrada J. M. (2007) — Sulphur, oxygen and strontium isotope compositions of Middle Miocene (Badenian) calcium sulphates from the Carpathian Foredeep, Poland: palaeoenvironmental implications. Geol. Quart., 51 (3): 285–294. Warszawa.
dc.identifier.essn2082-5099
dc.identifier.issn1641-7291
dc.identifier.officialurlhttps://gq.pgi.gov.pl/article/view/7456
dc.identifier.urihttps://hdl.handle.net/20.500.14352/104242
dc.issue.number3
dc.journal.titleGeological Quarterly
dc.language.isoeng
dc.page.final294
dc.page.initial285
dc.publisherPolish Geological Institute - National Research Institute
dc.rights.accessRightsopen access
dc.subject.cdu550.42:553.635:551.782.1(438)
dc.subject.cdu56:502(438)
dc.subject.keywordCarpathian Foredeep
dc.subject.keywordBadenian
dc.subject.keywordsulphur, oxygen and strontium isotopes
dc.subject.keywordsulphate deposits
dc.subject.ucmGeoquímica
dc.subject.ucmMineralogía (Geología)
dc.subject.unesco2503.08 Isótopos Estables
dc.subject.unesco2506.10 Yacimientos Minerales
dc.titleSulphur, oxygen and strontium isotope compositions of Middle Miocene (Badenian) calcium sulphates from the Carpathian Foredeep, Poland: Palaeoenvironmental implications
dc.typejournal article
dc.type.hasVersionVoR
dc.volume.number51
dspace.entity.typePublication
relation.isAuthorOfPublicationa08b4ec4-c32a-4ee2-800a-7b5842bda48e
relation.isAuthorOfPublication.latestForDiscoverya08b4ec4-c32a-4ee2-800a-7b5842bda48e

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