Abstract

Current estimates for the composition of the lower continental crust show significant variation for the concentrations of the highly incompatible elements, including large uncertainties for the heat-producing elements. This has consequences for models of the formation of lower crust. For example, is lower continental crust inherently poor in incompatible elements or has it become so after extraction of partial melts caused by thermal incubation? Answering these questions will require better agreement between estimates for the chemistry of the lower crust. One issue is that granulite samples may have been altered during ascent. Xenoliths often experience contamination from the entraining alkaline magma, potentially resulting in elevated concentrations of incompatible trace elements when analysed by conventional bulk rock techniques. To avoid this, we assessed an in situ approach for reconstructing whole rock compositions with granulites from the Kapuskasing Structural Zone, Superior Province, Canada. As terrain samples, they have not been affected by host magma contamination, and as subrecent glacial exposures, they show minimal modern weathering. We used scanning electron microscope electron dispersive spectroscopy (SEM-EDS) phase mapping to establish the modal mineralogy. Major and trace element concentrations of mineral phases were determined by electron microprobe and laser ablation inductively coupled plasma mass spectrometry (LA-ICPMS), respectively. These concentrations were combined with the modal mineralogies to obtain reconstructed whole rock compositions, which were compared to conventional bulk rock analyses. The reconstructed data show good reproducibility relative to the conventional analyses for samples with massive textures. However, the conventional bulk rock chemistry systematically yields higher K concentrations, which are hosted in altered feldspars. Thus, even in terrain samples, minor alteration can lead to elevated incompatible element estimates that may not represent genuine lower continental crust.

Highlights

  • The chemical composition of the lower continental crust (LCC) is poorly constrained compared to the upper crust partly due to its inaccessibility and scarcity of exposed samples

  • The major and trace element concentrations obtained by X-ray fluorescence (XRF) and solution inductively coupled plasma mass spectrometry (ICPMS) are listed in Comparisons between the conventional bulk rock data and the reconstitution approach are shown in Figures 3 and 4

  • The accuracy of the reconstructed whole rock compositions can be evaluated by comparison to the bulk rock major and trace element compositions obtained by XRF and solution ICPMS, respectively

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Summary

Introduction

The chemical composition of the lower continental crust (LCC) is poorly constrained compared to the upper crust partly due to its inaccessibility and scarcity of exposed samples. This is one reason for the large variation in estimated trace element compositions between different models of lower crustal composition (Figure 1). Granulite xenoliths, which commonly show equilibrated granular textures, come from greater depths than terrains and are widely thought to be more representative of the deepest parts of the continental crust [6,8,9,10]

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