scispace - formally typeset
Open AccessJournal ArticleDOI

Abiotic passive nitrogen and methane enrichment during exhumation of subducted rocks: Primary multiphase fluid inclusions in high‐pressure rocks from the Cabo Ortegal Complex, NW Spain

Reads0
Chats0
TLDR
In this paper , primary multiphase fluid inclusions (MFI) were studied in one eclogite and two granulites from the Cabo Ortegal Complex (COC, NW Spain) by means of Raman imaging, Scanning Electron Microscopy with Energy Dispersive Spectroscopy (SEM‐EDS) and Focused Ion Beam (FIB)‐SEM.
Abstract
Primary multiphase fluid inclusions (MFI) were studied in one eclogite and two granulites from the Cabo Ortegal Complex (COC, NW Spain) by means of Raman imaging, Scanning Electron Microscopy with Energy Dispersive Spectroscopy (SEM‐EDS) and Focused Ion Beam ‐ Scanning Electron Microscopy (FIB)‐SEM. Complementary, secondary MFI in pyroxenites from COC were also investigated. MFI hosted in eclogite and granulites occur along growth zones or in 3D clusters in garnet porphyroblasts suggesting a primary origin at high‐pressure (HP) metamorphic conditions. The mineral assemblage of MFI is mainly composed of Fe‐Mg‐Ca‐carbonates and phyllosilicates ± graphite ± quartz ± corundum ± pyrite ± apatite ± rutile and a fluid phase composed of nitrogen ± methane ± carbon‐dioxide. The mineral proportions vary among the lithologies. Dominant carbonates and hydrous silicates are interpreted as step‐daughter minerals (crystals formed in the MFI after entrapment as a result of fluid–host interaction), whereas apatite, quartz and rutile are considered in part as accidentally trapped minerals since they also occur as crystal inclusions together with MFI in each rock type. Quartz and corundum occur together in MFI in ultramafic granulite and are regarded as step‐daughter minerals in this lithology. These observations suggest that the MFI are products of post‐entrapment reactions of a homogeneous COHN fluid system with the host mineral. Thermodynamic calculations in the CaFMAS‐COHN system confirmed that bulk composition of the MFI in eclogite is similar to the host garnet+COHN composition except for a potential lost of H2O. Carbonation and hydration reaction between the host (i.e. garnet or pyroxene) and the fluid inclusion results in the consumption of all CO2 and part of the H2O from the fluid phase producing Ca‐Fe‐Mg‐carbonates and hydrous step‐daughter minerals, mostly pyrophyllite and chlorite. Nitrogen content of the originally trapped COHN fluid in eclogite was estimated to have a maximum value of 10 mol% at peak HP conditions and 30–40 mol% at retrograde conditions that is within the range of the observed MFI in the residual fluid (13–68 mol%). Pseudosection modelling confirmed the stability of the phase assemblage in the MFI in a specific low‐pressure, low‐temperature stability field (between 300°C and 400°C at pressures < 1 GPa), caused by H2O‐ and CO2‐consuming reactions possibly in a single step. Our findings indicate that such processes in the exhuming HP units may play a role in global nitrogen and carbon cycling as well as potentially contributing to nitrogen and methane supply to subsurface–surface environments during devolatilization in the forearc regions of convergent plate margins.

read more

Content maybe subject to copyright    Report

Citations
More filters
Journal ArticleDOI

Favorable P−T−ƒO2 conditions for abiotic CH4 production in subducted oceanic crusts: A comparison between CH4-bearing ultrahigh- and CO2-bearing high-pressure eclogite

TL;DR: In this paper , the authors identified CH4-rich fluid inclusions in ultra-high pressure (UHP; i.e., coesite-bearing) eclogites from the Chinese southwestern (SW) Tianshan palaeosubduction zone, respectively.
Journal ArticleDOI

Nitrogen fractionation in mica metapelite under hot subduction conditions: Implications for nitrogen ingassing to the mantle

- 01 Apr 2023 - 
TL;DR: In this paper , the authors investigated Nitrogen partitioning between its main hosts using partly devolatilized natural quartz-muscovite-chlorite schist (mica schist), with NH4+-rich muscovites, under conditions corresponding to hot subduction: 3.0-7.8 GPa, 750-1090 °C, and oxygen fugacity (fO2) about the NNO buffer.
Journal ArticleDOI

Estimation of P-T entrapment conditions of a subduction fluid using elastic thermobarometry: A case study from Cabo Ortegal Complex, Spain

Tim Woollings
- 01 Jul 2023 - 
TL;DR: In this article , the authors used elastic geothermobarometry to define the entrapment conditions of metamorphic granulite in the Cabo Ortegal Complex, Spain.
Journal ArticleDOI

Redox species and oxygen fugacity of slab-derived fluids: Implications for mantle oxidation and deep carbon-sulfur cycling

TL;DR: In this article , phase equilibria modeling on altered oceanic crust (AOC) and serpentinites along typical subduction geotherms in the C-S-bearing system over a pressure range of 0.5-6 GPa was conducted.
References
More filters
Journal ArticleDOI

Abbreviations for names of rock-forming minerals

TL;DR: The list of the most common and useful rock-forming minerals likely numbers in the several hundreds as discussed by the authors, and an expansion to the list initiated by Kretz (1983) was proposed by Spear.
Journal ArticleDOI

An improved and extended internally consistent thermodynamic dataset for phases of petrological interest, involving a new equation of state for solids

TL;DR: In this paper, the Tait equation of state (TEOS) was used to model the temperature dependence of both the thermal expansion and bulk modulus in a consistent way, which has led to improved fitting of the phase equilibrium experiments.
Journal ArticleDOI

Trace element signature of subduction-zone fluids, melts and supercritical liquids at 120–180 km depth

TL;DR: Measurements of the composition of fluids and melts equilibrated with a basaltic eclogite at pressures equivalent to depths in the Earth and temperatures of 700–1,200 °C constrain the recycling rates of key elements in subduction-zone arc volcanism.
Journal ArticleDOI

The geodynamic equation of state: What and how

TL;DR: In this article, the problem of phase equilibrium is reduced to a linear optimization problem that is independent of the functional form used for the equations of state of individual phases of the aggregate.
Related Papers (5)