Sulfur Isotopic Signature of Earth Established by Planetesimal Volatile Evaporation
Document Type
Article
Publication Date
11-1-2021
Publication Title
Nature Geoscience
Volume
14
Issue
11
First page number:
806
Last page number:
811
Abstract
How and when Earth’s volatile content was established is controversial with several mechanisms postulated, including planetesimal evaporation, core formation and the late delivery of undifferentiated chondrite-like materials. The isotopes of volatile elements such as sulfur can be fractionated during planetary accretion and differentiation and thus are potential tracers of these processes. Using first-principles calculations, we examine sulfur isotope fractionation during core formation and planetesimal evaporation. We find no measurable sulfur isotope fractionation between silicate and metallic melts at core-forming conditions, indicating that the observed light sulfur isotope composition of the bulk silicate Earth relative to chondrites cannot be explained by metal–silicate fractionation. Our thermodynamic calculations show that sulfur evaporates mostly as H2S during planetesimal evaporation when nebular H2 is present. The observed bulk Earth sulfur isotope signature and abundance can be reproduced by evaporative loss of about 90% sulfur mainly as H2S from molten planetesimals before nebular H2 is dissipated. The heavy sulfur isotope composition of the Moon relative to the Earth is consistent with evaporative sulfur loss under 94–98% saturation condition during the Moon-forming giant impact. In summary, volatile evaporation from molten planetesimals before Earth’s formation probably played a key role in establishing Earth’s volatile element content.
Controlled Subject
Sulfur--Isotopes
Disciplines
Cosmochemistry | Earth Sciences
Repository Citation
Wang, W.,
Li, C.,
Brodholt, J. P.,
Huang, S.,
Walter, M. J.,
Li, M.,
Wu, Z.,
Huang, F.,
Wang, S.
(2021).
Sulfur Isotopic Signature of Earth Established by Planetesimal Volatile Evaporation.
Nature Geoscience, 14(11),
806-811.
http://dx.doi.org/10.1038/s41561-021-00838-6