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The origin and transport of water in the early Solar System is an important topic in both astrophysics and planetary science, with applications to protosolar disk evolution, planetary formation, and astrobiology. Of particular interest for understanding primordial water transport are the unequilibrated ordinary chondrites (UOCs), which have been affected by very limited alteration since their formation. Using X-ray diffraction and isotope ratio mass spectrometry, we determined the bulk mineralogy, H2O content, and D/H ratios of 21 UOCs spanning from petrologic subtypes 3.00–3.9. The studied UOC falls of the lowest subtypes contain approximately 1 wt% H2O, and water abundance globally decreases with increasing thermal metamorphism. In addition, UOC falls of the lowest subtypes have elevated D/H ratios as high as those determined for some outer Solar System comets. This does not easily fit with existing models of water in the protoplanetary disk, which suggest D/H ratios were low in the warm inner Solar System and increased radially. These new analyses confirm that OC parent bodies accreted a D-rich component, possibly originating from either the outer protosolar nebula or from injection of molecular cloud streamers. The sharp decrease of D/H ratios with increasing metamorphism suggests that the phase(s) hosting this D-rich component is readily destroyed through thermal alteration.  相似文献   
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Abstract– The insoluble organic matter (IOM) of an unequilibrated enstatite chondrite Sahara (SAH) 97096 has been investigated using a battery of analytical techniques. As the enstatite chondrites are thought to have formed in a reduced environment at higher temperatures than carbonaceous chondrites, they constitute an interesting comparative material to test the heterogeneities of the IOM in the solar system and to constrain the processes that could affect IOM during solar system evolution. The SAH 97096 IOM is found in situ: as submicrometer grains in the network of fine‐grained matrix occurring mostly around chondrules and as inclusions in metallic nodules, where the carbonaceous matter appears to be more graphitized. IOM in these two settings has very similar δ15N and δ13C; this supports the idea that graphitized inclusions in metal could be formed by metal catalytic graphitization of matrix IOM. A detailed comparison between the IOM extracted from a fresh part and a terrestrially weathered part of SAH 97096 shows the similarity between both IOM samples in spite of the high degree of mineral alteration in the latter. The isolated IOM exhibits a heterogeneous polyaromatic macromolecular structure, sometimes highly graphitized, without any detectable free radicals and deuterium‐heterogeneity and having mean H‐ and N‐isotopic compositions in the range of values observed for carbonaceous chondrites. It contains some submicrometer‐sized areas highly enriched in 15N (δ15N up to 1600‰). These observations reinforce the idea that the IOM found in carbonaceous chondrites is a common component widespread in the solar system. Most of the features of SAH 97096 IOM could be explained by the thermal modification of this main component.  相似文献   
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