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Carbon isotope "stratigraphy" in a single graphite crystal: Implications for the crystal growth mechanism of fluid-deposited graphite

¹ Department of Natural Environmental Science, Faculty of Science, Kochi University, Akebono-cho 2-5-1, Kochi 780-8520, Japan
² Department of Biology and Geosciences, Faculty of Science, Shizuoka University, Ohya, Shizuoka 422-8529, Japan

Correspondence: ^* E-mail: satish{at}se-geomail.sci.shizuoka.ac.jp

A 2 cm long and 0.8 cm thick, single graphite crystal embedded in quartz, feldspar, and orthopyroxene of a granulite-facies metamorphic rock from southern India exhibits unique homogeneity in ¹³C values along layers parallel to the (0001) surface and smooth unidirectional variation of about 1 along the c-crystallographic axis. The fluid-precipitated graphite shows isotope homogeneity indicative of crystal growth along the (0001) plane. The C-isotope data along with the textural features suggest that the formation of graphite initiates in a layer perpendicular to the c-axis, possibly by a spiral growth mechanism. The initial layer is followed layer after layer, until the final stages of graphite growth. A second stage of graphite growth unrestricted by surrounding minerals is inferred from the un-deformed idiomorphic hexagonal form of the overgrown crystals. The C-isotope values in the overgrown rim of the crystal are lowered by about 2, suggesting a multistage precipitation. Morphologic and stable isotope studies thus confirm uniform crystal growth of graphite recording an isotope evolution pattern relating to fractionation from a fluid in an infinite reservoir during the main crystal formation. Spiral growth parallel to the (0001) face can explain the perfect uniformity of stable isotope composition in a single layer, whereas the variation across the (0001) surface gives insights into the time-integrated fluid evolution attending the crystal growth.