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Archean cordierite-orthopyroxene rocks from the eastern Beartooth Mountains, Montana, USA: insights into the local metamorphic pressure–temperature history

Published online by Cambridge University Press:  12 September 2025

Larry Tuttle*
Affiliation:
Department of Geology, Division of Natural Sciences, University of Maine at Farmington, Farmington, ME, USA
Darrell J. Henry
Affiliation:
Department of Geology and Geophysics, Louisiana State University, Baton Rouge, LA, USA
David W. Mogk
Affiliation:
Department of Earth Sciences, Montana State University, Bozeman, MT, USA
Paul A. Mueller
Affiliation:
Department of Geological Sciences, University of Florida, Gainesville, FL, USA
Celina Will
Affiliation:
Schlumberger, Denver, CO, USA
*
Corresponding author: Larry Tuttle; Email: larry.tuttle@maine.edu
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Abstract

The metamorphic history of the eastern Beartooth Mountains of Montana in the northern Archean Wyoming Province is challenging to establish given the multi-staged nature of metamorphism in the area and the prevalence of metamorphic overprinting. A petrologically illustrative cordierite-orthopyroxene xenolith in ∼2.80 Ga calc-alkaline granitic igneous rocks exhibits a mineral assemblage responsive to multiple metamorphic overprints. Cordierite-orthopyroxene and/or -orthoamphibole rocks (CORs) have mineral assemblages that provide instructive information on the metamorphic development of the terranes and the processes that form their protoliths. This investigation combines detailed petrographic and mineral-chemical investigations with petrological modelling of this COR locality, to establish important aspects of the local pressure-temperature (P-T) history.

The COR lithology, found in the Quad Creek locality of the study area, preserves textural evidence for three discrete metamorphic events consisting of a granulite-facies event (M1) that is overprinted by two, lower-grade hydration events: an upper amphibolite-facies event (M2) and a greenschist-facies event (M3). The M1 event is characterised by the mineral assemblage rutile-biotite-orthopyroxene-cordierite-quartz-melt ± sillimanite that equilibrated at ∼0.60 GPa and 775–815°C. M2 overprinting is marked by partial hydration of orthopyroxene to anthophyllite, crystallisation of plagioclase from a putative melt and ilmenite–rutile co-existence. The final metamorphic stage, M3, is marked by local hydration of orthorhombic inosilicates to talc and cordierite to pinite (chlorite). Estimates of M2 P-T conditions suggest development below ∼0.40 GPa at 615–725°C, whereas M3 probably developed below 0.40 GPa and 500–600°C. The resultant clockwise cordierite-orthopyroxene P-T path resembles modelled metamorphic P-T paths in proximal xenolithic lithologies. This interpretive P-T history is consistent with metamorphism in an Archean continental arc subduction zone with M1 metamorphism due to compression and tectonic burial, M2 due to hydration following, or coeval, with emplacement of voluminous ∼2.80 Ga plutons and M3 due to later low-T fluids. Although not conclusive, the Quad Creek COR was probably derived from a metasomatised basaltic protolith from the Archean seafloor, a comparable mode of origin to many COR occurrences worldwide.

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Article
Copyright
© The Author(s), 2025. Published by Cambridge University Press on behalf of The Mineralogical Society of the United Kingdom and Ireland.
Figure 0

Figure 1. Geological map from Mogk et al. (2022) showing the Wyoming Province and its three principle subdivisions: the Montana Metasedimentary terrane (MMT); Beartooth-Bighorn magmatic zone (BBMZ); and Southern Accreted Terrane (SAT), relative to surrounding terranes. Petrological divisions of the Beartooth Mountains are labelled thus: NSB – North Snowy block, SSB – South Snowy block, SC – Stillwater block and BT – Beartooth Plateau block. US state abbreviations are also indicated: MT – Montana, WY – Wyoming, etc.

Figure 1

Figure 2. Map of the Beartooth Mountains modified after Mueller et al. (1992). The Quad Creek COR xenolith is from the eastern edge of the Beartooth Plateau block, denoted by ‘QC’.

Figure 2

Table 1. Observed mineral assemblages for each Quad Creek COR sample from EMPA in this study. Representative scans of COR thin sections and corresponding rock chips for an unaltered sample (QC 82-19) and an altered sample (QC 21-14) are found in Supplementary material S2

Figure 3

Figure 3. COR photomicrographs showing a typical orthopyroxene porphyroblast with anthophyllite developed along the rim: (a) plane-polarised light (PPL) photomicrograph; (b) cross-polarised light (XPL) photomicrograph. Abbreviations from Warr (2021).

Figure 4

Figure 4. COR photomicrographs showing the relationship between plagioclase and surrounding matrix mineral phases: (a) PPL photomicrograph in which the plagioclase is difficult to distinguish; (b) optical cathodoluminescence photomicrograph in which plagioclase appears as white grains along the margins of apatite (light yellow), biotite (black), cordierite (dark red) and quartz (patchy dark blue/purple). Abbreviations from Warr (2021).

Figure 5

Figure 5. Photomicrographs of an extensively altered COR sample in which inosilicates are rimmed by talc and cordierite is completely replaced by pinite: (a) PPL photomicrograph; (b) optical cathodoluminescence photomicrograph.

Figure 6

Table 2. Average Quad Creek COR mineral compositions for each mineral targeted for major- and minor-element constituents

Figure 7

Figure 6. Orthopyroxene mineral chemistry: (a) Mg# (i.e. (Mg/Mg+Fe2+)) vs Ca content; (b) Mg# vs Al content.

Figure 8

Figure 7. Mg# of cordierite relative to Na content used to calculate Na-in-cordierite geothermometry temperatures.

Figure 9

Figure 8. Biotite composition (a) Mg# vs Al content with biotite end-member fields shown; (b) Mg# vs Ti content shown relative to Henry et al. (2005) TiB thermometry isotherms (alternating tan dashed lines and black solid lines) to indicate the resultant calculated TiB temperature for each biotite measurement shown.

Figure 10

Figure 9. Orthoamphibole compositions plotted relative to the classification scheme of Hawthorne et al. (2012) that is based on Al+Fe3++Ti in the c crystallographic site and the Mg#.

Figure 11

Figure 10. Plagioclase compositions expressed in terms of the feldspar ternary end-members: orthoclase (Or), albite (Ab) and anorthite (An).

Figure 12

Figure 11. Trace-element mineral compositions histograms: (a) Ti-in-quartz; (b) Zr-in-rutile. Overlain on each histogram are isotherms (alternating dashed and solid black lines) for the trace-element thermometer calibration used (i.e. Thomas et al., 2010, TitaniQ calibration and Tomkins et al., 2007, Zrt calibration) at an assumed equilibration pressure of 0.60 GPa.

Figure 13

Table 3. Average, smallest and largest Ti-in-quartz (TitaniQ) and Zr-in-rutile (Zrt) trace-element contents for the samples analysed

Figure 14

Figure 12. Representative photomicrographs of various samples showing patchy subgrains typified by COR matrix quartz: (a) optical cathodoluminescence photomicrograph (OM-CL); (b) scanning electron cathodoluminescence (SEM-CL) photomicrograph. Red-pink grain patches in OM-CL imagery and dark grey patches in SEM-CL imagery correspond to lower Ti contents and thus lower calculated TitaniQ temperatures relative to blue OM-CL grain patches and light grey SEM-CL grain patches.

Figure 15

Figure 13. Trace-element isopleth thermobarometry results showing the maximum isopleths (and associated error bars) for the TitaniQ (blue) and Zrt (orange) thermometers that intersect in P-T space at ∼0.60 GPa and 780ºC. The P-T region of combined TitaniQ-Zrt uncertainty is also shown around the area of isopleth intersection.

Figure 16

Figure 14. MnNCKFMASHTO pseudosection diagram for the EP-1957 bulk composition. Consistent with the published bulk composition of Eckelmann and Poldervaart (1957) pseudosection calculations utilised ∼6.50 moles of water and assumed all iron to be ferrous. The calculated pseudosection diagram is saturated with respect to quartz. Modelled mineral assemblage stability fields are numbered (assemblages corresponding to those numbers are given in the list of mineral assemblages to the right of the diagram) and mineral assemblages noted in petrography and discussed in the text are coloured. Additionally, the solidus is coloured in orange and the region of ilmenite–rutile co-stability is marked in gold. Mineral thermobarometry results are starred and the final breakdown reactions of both anthophyllite (dotted line) and plagioclase (dashed line) are highlighted. Garnet-bearing assemblages that are predicted at pressures above the bolded black line have been removed from the diagram. Mineral abbreviations are from Warr (2021).

Figure 17

Table 4. Published Quad Creek COR whole-rock composition constraints (in wt.% oxide) for sample ‘14/55’ from Eckelmann and Poldervaart (1957)

Figure 18

Figure 15. Interpreted clockwise P-T path (black arrows) for the Quad Creek COR based on P-T modelling efforts relative to the calculated MnNCKFMASHTO pseudosection diagram for the EP-1957 bulk composition. Conditions for each interpreted metamorphic event (i.e. M1, M2 and M3) are noted. Given that M1 conditions are well-constrained, these P-T conditions are boxed in dark green.

Figure 19

Figure 16. Orthoamphibole compositons of Quad Creek COR anthophyllite (represented by dashed black lines) and anthophyllite from analogous COR localities plotted relative to the classification scheme of Hawthorne et al. (2012) that is based on Al+Fe3++Ti in the c crystallographic site and the Mg#. The Quad Creek COR anthophyllite dataset falls neatly within the range defined by the datasets from the literature.

Figure 20

Figure 17. Comparisons between Quad Creek COR biotite and biotite from analogous global CORs: (a) Mg# vs Al content relative to compositional end-members; (b) Mg# vs Al content relative to Henry et al. (2005) TiB thermometry isopleths that indicate the resultant calculated TiB temperature for each biotite measurement. Biotite data from the literature, such as biotite from the Quad Creek COR (represented by black dashed lines), all classify as phlogopite. Quad Creek COR biotite chemistry largely falls within Al content and Mg# ranges defined by the literature data, however Quad Creek COR biotite Ti contents vary more considerably relative to that of literature analogues.

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