ترغب بنشر مسار تعليمي؟ اضغط هنا

Magmatic sulfides in the porphyritic chondrules of EH enstatite chondrites

147   0   0.0 ( 0 )
 نشر من قبل Laurette Piani
 تاريخ النشر 2016
  مجال البحث فيزياء
والبحث باللغة English




اسأل ChatGPT حول البحث

The nature and distribution of sulfides within 17 porphyritic chondrules of the Sahara 97096 EH3 enstatite chondrite have been studied by backscattered electron microscopy and electron microprobe in order to investigate the role of gas-melt interactions in the chondrule sulfide formation. Troilite (FeS) is systematically present and is the most abundant sulfide within the EH3 chondrite chondrules. It is found either poikilitically enclosed in low-Ca pyroxenes or scattered within the glassy mesostasis. Oldhamite (CaS) and niningerite [(Mg,Fe,Mn)S] are present in about 60% of the chondrules studied. While oldhamite is preferentially present in the mesostasis, niningerite associated with silica is generally observed in contact with troilite and low-Ca pyroxene. The chondrule mesostases contain high abundances of alkali and volatile elements as well as silica. Our data suggest that most of the sulfides found in EH3 chondrite chondrules are magmatic minerals that formed after the dissolution of S from a volatile-rich gaseous environment into the molten chondrules. Troilite formation occurred via sulfur solubility within Fe-poor chondrule melts followed by sulfide saturation, which causes an immiscible iron sulfide liquid to separate from the silicate melt. The FeS saturation started at the same time as or prior to the crystallization of low-Ca pyroxene during the high temperature chondrule forming event(s). Protracted gas-melt interactions under high partial pressures of S and SiO led to the formation of niningerite-silica associations via destabilization of the previously formed FeS and low-Ca pyroxene. We also propose that formation of the oldhamite occurred via the sulfide saturation of Fe-poor chondrule melts at moderate S concentration due to the high degree of polymerization and the high Na-content of the chondrule melts, which allowed the activity of CaO in the melt to be enhanced.

قيم البحث

اقرأ أيضاً

254 - Takashi Yoshizaki 2020
Chondrites are sediments of materials left over from the earliest stage of the solar system history. Based on their undifferentiated nature and less fractionated chemical compositions, chondrites are widely considered to represent the unprocessed bui lding blocks of the terrestrial planets and their embryos. Models of chemical composition of the terrestrial planets generally find chondritic relative abundances of refractory lithophile elements (RLE) in the bulk bodies (constant RLE ratio rule), based on limited variations of RLE ratios among chondritic meteorites and the solar photosphere. Here, we show that ratios of RLE, such as Nb/Ta, Zr/Hf, Sm/Nd and Al/Ti, are fractionated from the solar value in chondrules from enstatite chondrites (EC). The fractionated RLE ratios of individual EC chondrules document different chalcophile affinities of RLE under highly reducing environments and a separation of RLE-bearing sulfides from silicates before and/or during chondrule formation. In contrast, the bulk EC have solar-like RLE ratios, indicating that a physical sorting of silicates and sulfides was negligible before and during the accretion of EC parent bodies. Likewise, if the Earths accretion were dominated by EC-like materials, as supported by multiple isotope systematics, the physical sorting of silicates and sulfides in the accretionary disk should not have occurred among the Earths building blocks. Alternatively, the Earths precursors might have been high-temperature nebular materials that condensed before the RLE fractionation due to precipitation of the RLE-bearing sulfides...Highly reduced planets that have experienced selective removal or accretion of silicates or metal/sulfide phases, such as Mercury, might have fractionated, non-solar bulk RLE ratios.
The valence of iron has been used in terrestrial studies to trace the hydrolysis of primary silicate rocks. Here, we use a similar approach to characterize the secondary processes, namely thermal metamorphism and aqueous alteration, that have affecte d carbonaceous chondrites. X-ray absorption near-edge structure spectroscopy at the Fe-K- edge was performed on a series of 36 CM, 9 CR, 10 CV, and 2 CI chondrites. Among the four carbonaceous chondrites groups studied, a correlation between the iron oxidation index (IOI = [2 ((Fe2+) + 3(Fe3+))/FeTOT) and the hydrogen content is observed. However, within the CM group, for which a progressive alteration sequence has been defined, a conversion of Fe3+ to Fe2+ is observed with increasing degree of aqueous alteration. This reduction of iron can be explained by an evolution in the mineralogy of the secondary phases. In the case of the few CM chondrites that experienced some thermal metamorphism, in addition to aqueous alteration, a redox memory of the aqueous alteration is present: a significant fraction of 3+ 2+ 0 Fe is present, together with Fe and sometimes Fe. From our data set, the CR chondrites show a wider range of IOI from 1.5 to 2.5. In all considered CR chondrites, the three oxidation states of iron coexist. Even in the least-altered CR chondrites, the fraction of Fe3+ can be high (30% for MET 00426). This observation confirms that oxidized iron has been integrated during formation of fine-grained amorphous material in the matrix. Last, the IOI of CV chondrites does not reflect the reduced/oxidized classification based on metal and magnetite proportions, but is strongly correlated with petrographic types. The valence of iron in CV chondrites therefore appears to be most closely related to thermal history, rather than aqueous alteration, even if these processes can occur together .
Chondrites are one of the most primitive objects in the solar system, and keep the record of the degree of thermal metamorphism experienced in their parent bodies. This thermal history can be classified by the petrologic type. We investigate the ther mal evolution of planetesimals to account for the current abundances (known as the fall statistics) of petrologic types 3 - 6 ordinary chondrites. We carry out a number of numerical calculations in which formation times and sizes of planetesimals are taken as parameters. We find that planetesimals that form within 2.0 Myr after the formation of Ca-Al-rich inclusions (CAIs) can contain all petrologic types of ordinary chondrites. Our results also indicate that plausible scenarios of planetesimal formation, which are consistent with the fall statistics, are that planetesimals with radii larger than 60 km start to form around 2.0 Myr after CAIs and/or that ones with radii less than 50 km should be formed within 1.5 Myr after CAIs. Thus, thermal modelling of planetesimals is important for revealing the occurrence and amount of metamorphosed chondrites, and for providing invaluable insights into planetesimal formation.
We report microscopic, cathodoluminescence, chemical and O isotopic measurements of FeO-poor isolated olivine grains (IOG) in the carbonaceous chondrites Allende (CV3), Northwest Africa 5958 (C2-ung), Northwest Africa 11086 (CM2-an), Allan Hills 7730 7 (CO3.0). The general petrographic, chemical and isotopic similarity with bona fide type I chondrules confirms that the IOG derived from them. The concentric CL zoning, reflecting a decrease in refractory elements toward the margins, and frequent rimming by enstatite are taken as evidence of interaction of the IOG with the gas as stand-alone objects. This indicates that they were splashed out of chondrules when these were still partially molten. CaO-rich refractory forsterites, which are restricted to $Delta^{17}O < -4permil$ likely escaped equilibration at lower temperatures because of their large size and possibly quicker quenching. The IOG thus bear witness to frequent collisions in the chondrule-forming regions.
Terrestrial planets with large water inventories are likely ubiquitous and will be among the first Earth-sized planets to be characterized with upcoming telescopes. It has previously been argued that waterworlds-particularly those possessing more tha n 1% H$_2$O-experience limited melt production and outgassing due to the immense pressure overburden of their overlying oceans, unless subject to high internal heating. But an additional, underappreciated obstacle to outgassing on waterworlds is the high solubility of volatiles in high-pressure melts. Here, we investigate this phenomenon and show that volatile solubilities in melts probably prevent almost all magmatic outgassing from waterworlds. Specifically, for Earth-like gravity and oceanic crust composition, oceans or water ice exceeding 10-100 km in depth (0.1-1 GPa) preclude the exsolution of volatiles from partial melt of silicates. This solubility limit compounds the pressure overburden effect as large surface oceans limit both melt production and degassing from any partial melt that is produced. We apply these calculations to Trappist-1 planets to show that, given current mass and radius constraints and implied surface water inventories, Trappist-1f and -1g are unlikely to experience volcanic degassing. While other mechanisms for interior-surface volatile exchange are not completely excluded, the suppression of magmatic outgassing simplifies the range of possible atmospheric evolution trajectories and has implications for interpretation of ostensible biosignature gases, which we illustrate with a coupled model of planetary interior-climate-atmosphere evolution.
التعليقات
جاري جلب التعليقات جاري جلب التعليقات
سجل دخول لتتمكن من متابعة معايير البحث التي قمت باختيارها
mircosoft-partner

هل ترغب بارسال اشعارات عن اخر التحديثات في شمرا-اكاديميا