EGU21-10025, updated on 04 Mar 2021
https://doi.org/10.5194/egusphere-egu21-10025
EGU General Assembly 2021
© Author(s) 2021. This work is distributed under
the Creative Commons Attribution 4.0 License.

Evaluating the effects of deformation on the chemistry of composite magnesioferrite-magnetite crystals by means of EBSD

Igor González-Pérez1, Samuel Noval-Ruiz3, Jose María González-Jímenez1, Fernando Gervilla1,2, Isabel Fanlo3, and Fernando Tornos4
Igor González-Pérez et al.
  • 1Departamente de Mineralogía y Petrologia, Universidad de Granada, Granada, Spain (igorgonzpe@ugr.es)
  • 2Instituto Andaluz de Ciencias de la Tierra (IACT), CSIC-Universidad de Granada, Granada, Spain (gervilla@ugr.es)
  • 3Departamento de Ciencias de la Tierra, Cristalografía y Mineralogía, Universidad de Zaragoza, Zaragoza, Spain (fanlo@unizar.es)
  • 4Instituto de Geociencias, CSIC-Universidad Complutense de Madrid, Madrid, Spain (f.tornos@csic.es)

Chemical signatures of magnetite are commonly used to track the evolution of mineralizing systems in many geological settings. However, the impact of deformation processes on magnetite chemistry remains still underexplored. Here, we report a rare case of composite crystals consisting of magnetite and magnesioferrite recording different degrees and styles of deformation in order to evaluate how deformation promotes chemical modification. The samples employed in this study come from two different Mg-skarn iron deposits (i.e., El Robledal and San Manuel) from the Serranía de Ronda (SW Spain). Chemical data acquired by Electron Probe Microprobe Analyzer (EPMA) and Field Emission Scanning Microscopy (FESEM) are contrasted against microstructural data obtained by using Electron Back-Scattered Diffraction (EBSD). Our results show that magnesioferrite crystals [Fe2+# (Fe2+/Fe2++Mg2+) = 0.22-0.46 and Fe3+# (Fe3+/Fe3++Al3+) = 0.99-1.00] from El Robledal deposit are characterized by a ductile deformation that led to different crystallographic orientation domains along with the replacement of magnesioferrite by magnetite (Fe2+# (Fe2+/Fe2++Mg2+) = 0.51-0.99 and Fe3+ (Fe3+/Fe3++Al3+) =0.98-1.00] via coupled dissolution – reprecipitation. A replacement of magnesioferrite [Fe2+# (Fe2+/Fe2++Mg2+) = 0.43-0.64 and Fe3+ (Fe3+/Fe3++Al3+) = 0.99-1.00] by magnetite Fe2+# (Fe2+/Fe2++Mg2+) = 0.78-1.00 and Fe3+# (Fe3+/Fe3++Al3+) = 0.98-1.00] via a coupled dissolution – reprecipitation mechanism is also preserved in the composite (i.e., zoned) crystals from the San Manuel deposit, which was additionally overprinted by an additional recrystallization event as a result of grain boundary migration recrystallization. Our results show that deformation in a fluid-assisted deformation regime has induced chemical modification of the original magnesioferrite aggregates as well as strain localization. This close physicochemical link offers new avenues of interpreting the chemical signatures of Mg-Fe oxides, utilizing their microstructurally controlled variation or lack thereof.

How to cite: González-Pérez, I., Noval-Ruiz, S., González-Jímenez, J. M., Gervilla, F., Fanlo, I., and Tornos, F.: Evaluating the effects of deformation on the chemistry of composite magnesioferrite-magnetite crystals by means of EBSD, EGU General Assembly 2021, online, 19–30 Apr 2021, EGU21-10025, https://doi.org/10.5194/egusphere-egu21-10025, 2021.

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