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Porous,S‐bearing silica in metal‐sulfide nodules and in the interchondrule clastic matrix in two EH3 chondrites
Authors:S W Lehner  P Németh  M I Petaev  P R Buseck
Institution:1. School of Earth and Space Exploration, Arizona State University, Tempe, Arizona, USA;2. Institute of Materials and Environmental Chemistry, Research Center for Natural Sciences, Hungarian Academy of Sciences, Budapest, Hungary;3. Department of Earth and Planetary Sciences, Harvard University, Cambridge, Massachusetts, USA;4. Solar, Stellar, and Planetary Sciences, Harvard‐Smithsonian CfA, Cambridge, Massachusetts, USA
Abstract:Two new occurrences of porous, S‐bearing, amorphous silica are described within metal‐sulfide nodules (MSN) and as interchondrule patches in EH3 chondrites SAH 97072 and ALH 84170. This porous amorphous material, which was first reported from sulfide‐bearing chondrules, consists of sinewy SiO2‐rich areas containing S with minor Na or Ca as well as Fe, Mg, and Al. Some pores contain minerals including pyrite, pyrrhotite, and anhydrite. Most pores appear vacant or contain unidentified material that is unstable under analytical conditions. Niningerite, olivine, enstatite, albite, and kumdykolite occur enclosed within porous silica patches. Porous silica is commonly interfingered with cristobalite suggesting its amorphous structure resulted from high‐temperature quenching. We interpret the S‐bearing porous silica to be a product of silicate sulfidation, and the Na, Ca, Fe, Mg, and Al detectable within this material are chemical residues of sulfidized silicates and metal. The occurrence of porous silica in the cores of MSN, which are considered to be pre‐accretionary objects, suggests the sulfidizing conditions occurred prior to final parent‐body solidification. Ubiquitous S‐bearing porous silica among sulfide‐bearing chondrules, MSN, and in the interchondrule clastic matrix, suggests that similar sulfidizing conditions affected all the constituents of these EH3 chondrites.
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