Aquatic Geochemistry

, Volume 17, Issue 1, pp 71–108

Salt Waters of the Northern Apennine Foredeep Basin (Italy): Origin and Evolution

  • Tiziano Boschetti
  • Lorenzo Toscani
  • Orfan Shouakar-Stash
  • Paola Iacumin
  • Giampiero Venturelli
  • Claudio Mucchino
  • Shaun K. Frape
Original Paper

DOI: 10.1007/s10498-010-9107-y

Cite this article as:
Boschetti, T., Toscani, L., Shouakar-Stash, O. et al. Aquat Geochem (2011) 17: 71. doi:10.1007/s10498-010-9107-y

Abstract

The salt waters from the Emilia-Romagna sector of the Northern Apennine Foredeep have been investigated using major and trace element and stable isotope (δ2H, δ18O, δ37Cl, δ81Br and 87Sr/86Sr ratio). Ca, Mg, Na, K, Sr, Li, B, I, Br and SO4 vs. Cl diagrams suggest the subaerial evaporation of seawater beyond gypsum and before halite precipitation as primary process to explain the brine’s salinity, whereas saline to brackish waters were formed by mixing of evaporated seawater and water of meteoric origin. A diagenetic end-member may be a third component for mud volcanoes and some brackish waters. Salinization by dissolution of (Triassic) evaporites has been detected only in samples from the Tuscan side of the Apennines and/or interacting with the Tuscan Nappe. In comparison with the seawater evaporation path, Ca–Sr enrichment and Na–K–Mg depletion of the foredeep waters reveal the presence of secondary processes such as dolomitization–chloritization, zeolitization–albitization and illitization. Sulfate concentration, formerly buffered by gypsum-anhydrite deposition, is heavily lowered by bacterial and locally by thermochemical reduction during burial diagenesis. From an isotopic point of view, data of the water molecule confirm mixing between seawater and meteoric end-members. Local 18O-shift up to +11‰ at Salsomaggiore is related to water–rock interaction at high temperature (≈150°C) as confirmed by chemical (Mg, Li, Ca distribution) and isotopic (SO4–H2O) geothermometers. 37Cl/35Cl and 81Br/79Br ratios corroborate the marine origin of the brines and evidence the diffusion of halogens from the deepest and most saline aquifers toward the surface. The 87Sr/86Sr ratio suggests a Miocene origin of Sr and rule out the hypothesis of a Triassic provenance of the dissolved components for the analyzed waters issuing from the Emilia-Romagna sector of the foredeep. Waters issuing from the Tuscan side of the Apennines and from the Marche sector of the foredeep show higher 87Sr/86Sr ratios because of the interaction with siliciclastic rocks.

Keywords

Salt waters Chemical and isotope composition Seawater evaporation Northern Apennine Foredeep 

Supplementary material

10498_2010_9107_MOESM1_ESM.xls (140 kb)
Supplementary material 1 (XLS 138 kb)

Copyright information

© Springer Science+Business Media B.V. 2010

Authors and Affiliations

  • Tiziano Boschetti
    • 1
  • Lorenzo Toscani
    • 1
  • Orfan Shouakar-Stash
    • 2
  • Paola Iacumin
    • 1
  • Giampiero Venturelli
    • 1
  • Claudio Mucchino
    • 3
  • Shaun K. Frape
    • 2
  1. 1.Department of Earth SciencesUniversity of ParmaParmaItaly
  2. 2.Department of Earth SciencesUniversity of WaterlooWaterlooCanada
  3. 3.Department of Analytical ChemistryUniversity of ParmaParmaItaly

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