Crystallization of dmisteinbergite (hexagonal CaAl2Si2O8) from type B CAI analog melt

1Yasuaki Tsuruoka, 1,5Hideto Yoshida, 2,6Yuki Inoue, 2Daiki Yamamoto, 3Hiroyuki Kagi, 4Akira Miyake, 1Shogo Tachibana
Meteoritics & Planetary Science (in Press) Open Source Link to Article [DOI: 10.1111/maps.70213]

1Department of Earth and Planetary Science, The University of Tokyo, Bunkyo-ku, Tokyo, Japan
2Department of Earth and Planetary Sciences, Kyushu University, Nishi-ku, Fukuoka, Japan
3Geochemical Research Center, The University of Tokyo, Bunkyo-ku, Tokyo, Japan
4Department of Geology and Mineralogy, Kyoto University, Sakyo-ku, Kyoto, Japan
5The Kiso Observatory, Institute of Astronomy, The University of Tokyo, Kiso-machi, Nagano, Japan
6Atmosphere and Ocean Research Institute, The University of Tokyo, Kashiwa-shi, Chiba, Japan
Published by arrangement with John Wiley & Sons

Dmisteinbergite is a metastable polymorph of CaAl2Si2O8, which has been found in calcium−aluminum-rich inclusions (CAIs) in chondrites, although anorthite is the predominant CaAl2Si2O8 phase in natural type B CAIs. The occurrence/absence of igneous dmisteinbergite would put tighter constraints on the thermal history of CAIs. However, little attention has been paid for crystallization of dmisteinbergite in CAI melts even though its kinetically controlled crystallization (i.e., crystallization from a supercooled melt) has been proposed. In this study, we conducted dynamic crystallization experiments on CAI analogs in the presence of low-pressure hydrogen gas (1–10 Pa) to simulate the formation of igneous CAIs and to understand crystallization behavior of CaAl2Si2O8 phases. Dmisteinbergite was found in samples cooled at rates of 1–20 °C h−1, while anorthite was found in samples cooled at 5 °C h−1, suggesting that the slow cooling (likely slower than on the order of 1 °C h−1) might promote the formation of anorthite. Because the slow cooling rates during the final stage of crystallization of CAIs likely reflect conditions approaching the background temperature of CAI-forming regions, CaAl2Si2O8 phases in type B CAIs could constrain the thermal history and formation environment of those regions.

Dmisteinbergite is a metastable polymorph of CaAl2Si2O8, which has been found in calcium−aluminum-rich inclusions (CAIs) in chondrites, although anorthite is the predominant CaAl2Si2O8 phase in natural type B CAIs. The occurrence/absence of igneous dmisteinbergite would put tighter constraints on the thermal history of CAIs. However, little attention has been paid for crystallization of dmisteinbergite in CAI melts even though its kinetically controlled crystallization (i.e., crystallization from a supercooled melt) has been proposed. In this study, we conducted dynamic crystallization experiments on CAI analogs in the presence of low-pressure hydrogen gas (1–10 Pa) to simulate the formation of igneous CAIs and to understand crystallization behavior of CaAl2Si2O8 phases. Dmisteinbergite was found in samples cooled at rates of 1–20 °C h−1, while anorthite was found in samples cooled at 5 °C h−1, suggesting that the slow cooling (likely slower than on the order of 1 °C h−1) might promote the formation of anorthite. Because the slow cooling rates during the final stage of crystallization of CAIs likely reflect conditions approaching the background temperature of CAI-forming regions, CaAl2Si2O8 phases in type B CAIs could constrain the thermal history and formation environment of those regions.

Discuss