Hydroxyl in eclogitic garnet, orthopyroxene, and oriented inclusion-bearing clinopyroxene, western Norway.

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Title: Hydroxyl in eclogitic garnet, orthopyroxene, and oriented inclusion-bearing clinopyroxene, western Norway.
Authors: Spengler, Dirk1 (AUTHOR) dirk@spengler.eu, Koch-Müller, Monika2 (AUTHOR), Włodek, Adam1 (AUTHOR), Cuthbert, Simon J.1 (AUTHOR), Majka, Jarosław1,3 (AUTHOR)
Source: Solid Earth. 2025, Vol. 16 Issue 3, p233-250. 18p.
Subjects: Orthopyroxene, Extreme value theory, Eclogite, Minerals, Cratons, Garnet
Abstract: A total of 10 western Norwegian eclogites, whose mineral chemistry records metamorphism of up to 850 °C and 5.5 GPa , were investigated for structural hydroxyl content in nominally anhydrous minerals. Garnet shows pronounced absorption in the wavenumber ranges of 3596–3633, 3651–3694, and 3698–3735 cm-1 and minor absorption centred at about 3560 cm-1. Clinopyroxene with aligned inclusions of either quartz, albite, or quartz + pargasite has major absorption at 3450–3471 and 3521–3538 cm-1 and minor absorption centred at 3350 and approximately 3625 cm-1. The latter band is strongest in a sample with minute lamellar inclusions rich in Al, Fe, and Na and was excluded from hydroxyl quantification. Orthopyroxene has large, narrow absorption peaks centred at 3415 and 3515 cm-1 and smaller peaks at 3555, 3595, and 3625 cm-1. Five orthopyroxene-bearing eclogites exhibit relatively homogeneous amounts of structural hydroxyl in garnet (13–32 µgg-1), clinopyroxene (119–174 µgg-1), and orthopyroxene (4–17 µgg-1). The outer 200 µm wide rims of the orthopyroxene grains illustrate a late hydroxyl loss compared to core values of about 30 %, which is not evident in garnet and clinopyroxene. In contrast, the other five orthopyroxene-free eclogites exhibit variable amounts of hydroxyl in garnet (8–306 µgg-1) and clinopyroxene (58–711 µgg-1). Apart from extreme values, the structural hydroxyl content of clinopyroxene in the eclogites studied is lower than in comparable ultra-high-pressure metamorphic samples, e.g. both metasomatised and pristine eclogite xenoliths from the lithospheric mantle underneath several cratons and coesite- and quartz-eclogites from the Erzgebirge and the Kokchetav massifs, by up to several hundreds of micrograms per gram (µgg-1). The low structural hydroxyl contents, the deficiency of molecular water, and the preservation of diffusion-sensitive evidence from the mineral chemistry for metamorphism well beyond the stability field of amphibole suggest that oriented inclusions of quartz + pargasite were formed isochemically during decompression. In addition, structural hydroxyl content in clinopyroxene is inversely correlated with metamorphic pressure estimates obtained from orthopyroxene of the same samples. Therefore, structural hydroxyl in nominally anhydrous eclogite minerals can serve as an indicator of the effectiveness of retrogression. [ABSTRACT FROM AUTHOR]
Copyright of Solid Earth is the property of Copernicus Gesellschaft mbH and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)
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  Label: Title
  Group: Ti
  Data: Hydroxyl in eclogitic garnet, orthopyroxene, and oriented inclusion-bearing clinopyroxene, western Norway.
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  Data: <searchLink fieldCode="JN" term="%22Solid+Earth%22">Solid Earth</searchLink>. 2025, Vol. 16 Issue 3, p233-250. 18p.
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  Data: <searchLink fieldCode="DE" term="%22Orthopyroxene%22">Orthopyroxene</searchLink><br /><searchLink fieldCode="DE" term="%22Extreme+value+theory%22">Extreme value theory</searchLink><br /><searchLink fieldCode="DE" term="%22Eclogite%22">Eclogite</searchLink><br /><searchLink fieldCode="DE" term="%22Minerals%22">Minerals</searchLink><br /><searchLink fieldCode="DE" term="%22Cratons%22">Cratons</searchLink><br /><searchLink fieldCode="DE" term="%22Garnet%22">Garnet</searchLink>
– Name: Abstract
  Label: Abstract
  Group: Ab
  Data: A total of 10 western Norwegian eclogites, whose mineral chemistry records metamorphism of up to 850 °C and 5.5 GPa , were investigated for structural hydroxyl content in nominally anhydrous minerals. Garnet shows pronounced absorption in the wavenumber ranges of 3596–3633, 3651–3694, and 3698–3735 cm-1 and minor absorption centred at about 3560 cm-1. Clinopyroxene with aligned inclusions of either quartz, albite, or quartz + pargasite has major absorption at 3450–3471 and 3521–3538 cm-1 and minor absorption centred at 3350 and approximately 3625 cm-1. The latter band is strongest in a sample with minute lamellar inclusions rich in Al, Fe, and Na and was excluded from hydroxyl quantification. Orthopyroxene has large, narrow absorption peaks centred at 3415 and 3515 cm-1 and smaller peaks at 3555, 3595, and 3625 cm-1. Five orthopyroxene-bearing eclogites exhibit relatively homogeneous amounts of structural hydroxyl in garnet (13–32 µgg-1), clinopyroxene (119–174 µgg-1), and orthopyroxene (4–17 µgg-1). The outer 200 µm wide rims of the orthopyroxene grains illustrate a late hydroxyl loss compared to core values of about 30 %, which is not evident in garnet and clinopyroxene. In contrast, the other five orthopyroxene-free eclogites exhibit variable amounts of hydroxyl in garnet (8–306 µgg-1) and clinopyroxene (58–711 µgg-1). Apart from extreme values, the structural hydroxyl content of clinopyroxene in the eclogites studied is lower than in comparable ultra-high-pressure metamorphic samples, e.g. both metasomatised and pristine eclogite xenoliths from the lithospheric mantle underneath several cratons and coesite- and quartz-eclogites from the Erzgebirge and the Kokchetav massifs, by up to several hundreds of micrograms per gram (µgg-1). The low structural hydroxyl contents, the deficiency of molecular water, and the preservation of diffusion-sensitive evidence from the mineral chemistry for metamorphism well beyond the stability field of amphibole suggest that oriented inclusions of quartz + pargasite were formed isochemically during decompression. In addition, structural hydroxyl content in clinopyroxene is inversely correlated with metamorphic pressure estimates obtained from orthopyroxene of the same samples. Therefore, structural hydroxyl in nominally anhydrous eclogite minerals can serve as an indicator of the effectiveness of retrogression. [ABSTRACT FROM AUTHOR]
– Name: AbstractSuppliedCopyright
  Label:
  Group: Ab
  Data: <i>Copyright of Solid Earth is the property of Copernicus Gesellschaft mbH and its content may not be copied or emailed to multiple sites without the copyright holder's express written permission. Additionally, content may not be used with any artificial intelligence tools or machine learning technologies. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract.</i> (Copyright applies to all Abstracts.)
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      – Type: doi
        Value: 10.5194/se-16-233-2025
    Languages:
      – Code: eng
        Text: English
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      Pagination:
        PageCount: 18
        StartPage: 233
    Subjects:
      – SubjectFull: Orthopyroxene
        Type: general
      – SubjectFull: Extreme value theory
        Type: general
      – SubjectFull: Eclogite
        Type: general
      – SubjectFull: Minerals
        Type: general
      – SubjectFull: Cratons
        Type: general
      – SubjectFull: Garnet
        Type: general
    Titles:
      – TitleFull: Hydroxyl in eclogitic garnet, orthopyroxene, and oriented inclusion-bearing clinopyroxene, western Norway.
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            NameFull: Koch-Müller, Monika
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            NameFull: Włodek, Adam
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            NameFull: Majka, Jarosław
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              Text: 2025
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