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Carbonate formation events in ALH 84001 trace the evolution of the Martian atmosphere.


ABSTRACT: Carbonate minerals provide critical information for defining atmosphere-hydrosphere interactions. Carbonate minerals in the Martian meteorite ALH 84001 have been dated to ? 3.9 Ga, and both C and O-triple isotopes can be used to decipher the planet's climate history. Here we report ?(17)O, ?(18)O, and ?(13)C data of ALH 84001 of at least two varieties of carbonates, using a stepped acid dissolution technique paired with ion microprobe analyses to specifically target carbonates from distinct formation events and constrain the Martian atmosphere-hydrosphere-geosphere interactions and surficial aqueous alterations. These results indicate the presence of a Ca-rich carbonate phase enriched in (18)O that formed sometime after the primary aqueous event at 3.9 Ga. The phases showed excess (17)O (0.7‰) that captured the atmosphere-regolith chemical reservoir transfer, as well as CO2, O3, and H2O isotopic interactions at the time of formation of each specific carbonate. The carbon isotopes preserved in the Ca-rich carbonate phase indicate that the Noachian atmosphere of Mars was substantially depleted in (13)C compared with the modern atmosphere.

SUBMITTER: Shaheen R 

PROVIDER: S-EPMC4299197 | biostudies-literature | 2015 Jan

REPOSITORIES: biostudies-literature

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Carbonate formation events in ALH 84001 trace the evolution of the Martian atmosphere.

Shaheen Robina R   Niles Paul B PB   Chong Kenneth K   Corrigan Catherine M CM   Thiemens Mark H MH  

Proceedings of the National Academy of Sciences of the United States of America 20141222 2


Carbonate minerals provide critical information for defining atmosphere-hydrosphere interactions. Carbonate minerals in the Martian meteorite ALH 84001 have been dated to ∼ 3.9 Ga, and both C and O-triple isotopes can be used to decipher the planet's climate history. Here we report Δ(17)O, δ(18)O, and δ(13)C data of ALH 84001 of at least two varieties of carbonates, using a stepped acid dissolution technique paired with ion microprobe analyses to specifically target carbonates from distinct form  ...[more]

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