Simultaneous operation of opposing reaction mechanisms: The influence of matrix heterogeneity on post-kinematic garnet crystallization in an inverted metamorphic sequence

Metapelites from the inverted Barrovian sequence in the Sikkim Himalaya (northeast India) are shown to be largely continuous with respect to their bulk rock compositions, microstructures and pressure–temperature–time–deformation (P–T–t–D) histories. However, the upper garnet–lower staurolite zone demarcates a region of microstructurally anomalous post-kinematic garnet populations contained within strongly segregated matrices. The different microstructures within samples from this region cannot be attributed to differences in their thermobarometric histories or bulk compositions, but are instead interpreted to represent an otherwise unexposed level of the Daling Group that is now exposed along a post-metamorphic thrust splay. These heterogeneous samples contain several discrete garnet populations that progressively crystallized with increasing P–T. Garnet populations that experienced the most protracted growth now form complex polycrystals that exhibit crystallographically controlled and morphologically irregular interfaces adjacent to micaceous and quartzofeldspathic domains respectively. Electron backscatter diffraction indicates that these polycrystalline garnet structures contain numerous coalesced porphyroblasts that are structurally uncorrelated across their grain boundaries. However, a crystallographically preferred orientation at the polycrystal scale is interpreted to derive from epitaxial crystallization of early-formed garnet porphyroblasts on precursor mica. Later-nucleated porphyroblasts within polycrystals preferentially concentrated towards quartzofeldspathic domains, with the overall nucleation distribution likely controlled by a complex interplay between chemical heterogeneities, strain partitioning and epitaxial crystallization. The subsequent growth of these polycrystals was equally spatially heterogeneous; it was moderated by differences in the efficiency of grain boundary transfer between quartzofeldspathic and micaceous domains that precluded thin section-scale chemical equilibration. In contrast to samples from Sikkim containing more typical porphyroblastic populations in continuous and disseminated matrices, heterogeneous availability of garnet-forming components within this strongly layered matrix is shown to have resulted in grain-scale variations in growth rates and the spatial juxtapositioning of interface-controlled microstructures and locally equilibrated chemical compositions with those that were transport controlled.     

NIST RM 8301 Boron Isotopes in Marine Carbonate (Simulated Coral and Foraminifera Solutions): Inter‐laboratory δ11B and Trace Element Ratio Value Assignment

The boron isotopic ratio of ¹¹B/¹⁰B (δ¹¹B_SRM951) and trace element composition of marine carbonates are key proxies for understanding carbon cycling (pH) and palaeoceanographic change. However, method validation and comparability of results between laboratories requires carbonate reference materials. Here, we report results of an inter‐laboratory comparison study to both assign δ¹¹B_SRM951 and trace element compositions to new synthetic marine carbonate reference materials (RMs), NIST RM 8301 (Coral) and NIST RM 8301 (Foram) and to assess the variance of data among laboratories. Non‐certified reference values and expanded 95% uncertainties for δ¹¹B_SRM951 in NIST RM 8301 (Coral) (+24.17‰ ± 0.18‰) and NIST RM 8301 (Foram) (+14.51‰ ± 0.17‰) solutions were assigned by consensus approach using inter‐laboratory data. Differences reported among laboratories were considerably smaller than some previous inter‐laboratory comparisons, yet discrepancies could still lead to large differences in calculated seawater pH. Similarly, variability in reported trace element information among laboratories (e.g., Mg/Ca ± 5% RSD) was often greater than within a single laboratory (e.g., Mg/Ca < 2%). Such differences potentially alter proxy‐reconstructed seawater temperature by more than 2 °C. These now well‐characterised solutions are useful reference materials to help the palaeoceanographic community build a comprehensive view of past ocean changes.