About: Niningerite is a research topic. Over the lifetime, 56 publications have been published within this topic receiving 2330 citations. The topic is also known as: IMA1966-036.
TL;DR: In this paper, 15 enstatite chondrites were studied microscopically in reflected and transmitted light, and their modal compositions were determined by point-counting techniques.
Abstract: Fifteen of the sixteen known enstatite chondrites were studied microscopically in reflected and transmitted light, and their modal compositions were determined by point-counting techniques. Compositions of clinoenstatite, orthoenstatite, plagioclase, kamacite, taenite, troilite, oldhamite, daubreelite, niningerite, ferroan alabandite, and schreibersite were determined with the electron microprobe X-ray analyzer. Chemical composition, mineral occurrence, and mineral composition were found to depend on degree of recrystallization of the chondrites as judged by, for example, distinctness of chondrules and coarseness of silicates. On the basis of these parameters, three groups of enstatite chondrites can be distinguished and are referred to as type I, intermediate type, and type II. Differences between types I and II are pronounced, whereas intermediate type is transitional. The suggestion of Van Schmus and Wood that type II enstatite chondrites originated from type I by reheating is reviewed in the light of the new data. It is concluded that, although many of the chemical-mineralogical parameters of type II chondrites could be explained as being the result of reheating of type I chondrites, there are some that would require rather stringent environmental conditions during reheating. For example, lower iron and sulfur contents in type II chondrites would presumably require reheating of type I chondrites to ≥975°C, the lowest temperature at which a melt would appear in the Fe-Ni-S system of type I composition and at which physical separation of the liquid from the silicates could occur. Differences in Si/Mg ratios would require reheating to even higher temperatures and fractionation in an open system. Furthermore, observed differences in nitrogen and sinoite contents between type I and type II are difficult to explain unless reheating took place in a closed system, or under oxygen fugacities low enough to allow nitrogen to react with SiO2 and Si to form Si2N2O. An alternative model to the one by Van Schmus and Wood is discussed; it assumes that major differences in chemical and mineralogical composition between type I and type II were essentially established before or during chondrule formation and agglomeration by, for example, igneous differentiation or fractionation during condensation from a solar nebula, and that differences in texture are due either to different cooling rates of type I and type II chondrites during and after agglomeration of chondrules or to mild reheating to temperatures ≤975°C. This model does not, however, readily explain why only enstatite chondrites of type II bulk chemical composition (i.e. low Fe, S) cooled slowly or were reheated, and why chondrites of type I composition (high Fe, S) were always quenched to temperatures low enough to prevent recrystallization and were not reheated.
TL;DR: The enstatite chondrites formed under highly reducing (and/or sulfidizing) conditions as indicated by their mineral assemblages and compositions, which are sharply different from those of other chondrite groups as mentioned in this paper.
Abstract: The enstatite chondrites formed under highly reducing (and/or sulfidizing) conditions as indicated by their mineral assemblages and compositions, which are sharply different from those of other chondrite groups. Enstatite is the major silicate mineral. Kamacite is Si-bearing and the enstatite chondrites contain a wide variety of monosulfide minerals that are not present in other chondrite groups. The unequilibrated enstatite chondrites are comprised of two groups (EH3 and EL3) and one anomalous member (LEW 87223), which can be distinguished by differences in their mineral assemblages and compositions. EH3 chondrites have >1.8 wt.% Si in their kamacite and contain the monosulfide niningerite (MgS), whereas EL3 chondrites have less than 1.4 wt.% Si in their kamacite and contain the monosulfide alabandite (MnS). The distinct mineralogies, compositions and textures of E3 chondrites make comparisons with ordinary chondrites (OCs) and carbonaceous chondrites (CCs) difficult, however, a range of recrystallization features in the E3s are observed, and some may be as primitive as type 3.1 OCs and CCs. Others, especially the EL3 chondrites, may have been considerably modified by impact processes and their primary textures disturbed. The chondrules in E3 chondrites, although texturally similar to type I pyroxene-rich chondrules, are sharply different from chondrules in other chondrite groups in containing Si-bearing metal, Ca- and Mg–Mn-rich sulfides and silica. This indicates formation in a reduced nebular environment separate from chondrules in other chondrites and possibly different precursor materials. Additionally the oxygen isotope compositions of E3 chondrules indicate formation from a unique oxygen reservoir. Although the abundance, size distribution, and secondary alteration minerals are not always identical, CAIs in E3 chondrites generally have textures, mineral assemblages and compositions similar to those in other groups. These observations indicates that CAIs in O, C and E chondrites all formed in the reservoir under similar conditions, and were redistributed to the different chondrite accretion zones, where the secondary alteration took place. Thus, chondrule formation was a local process for each particular chondrite group, but all CAIs may have formed in the similar nebular environment. Lack of evidence of water (hydrous minerals), and oxygen isotope compositions similar to Earth and Moon suggest formation of the E chondrites in the inner solar system and make them prime candidates as building blocks for the inner planets.
TL;DR: Liu et al. as discussed by the authors obtained Raman spectra from a series of natural and synthetic sulfideminerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr 2 FeS 4 ).
Abstract: –Raman spectra were acquired on a series of natural and synthetic sulfideminerals, commonly found in enstatite meteorites: oldhamite (CaS), niningerite or keilite((Mg,Fe)S), alabandite (MnS), troilite (FeS), and daubreelite (Cr 2 FeS 4 ). Natural samplescome from three enstatite chondrites, three aubrites, and one anomalous ungroupedenstatite meteorite. Synthetic samples range from pure endmembers (CaS, FeS, MgS) tocomplex solid solutions (Fe, Mg, Ca)S. The main Raman peaks are localized at 225, 285,360, and 470 cm 1 for the Mg-rich sulfides; at 185, 205, and 285 cm 1 for the Ca-richsulfides; at 250, 370, and 580 cm 1 for the Mn-rich sulfides; at 255, 290, and 365 cm 1 for the Cr-rich sulfides; and at 290 and 335 cm 1 for troilite with, occasionally, an extrapeak at 240 cm 1 . A peak at 160 cm 1 is present in all Raman spectra and cannot beused to discriminate between the different sulfide compositions. According to grouptheory, none of the cubic monosulfides oldhamite, niningerite, or alabandite shouldpresent first-order Raman spectra because of their ideal rocksalt structure. The occurrenceof broad Raman peaks is tentatively explained by local breaking of symmetry rules.Measurements compare well with the infrared frequencies calculated from first-principlescalculations. Raman spectra arise from activation of certain vibrational modes due toclustering in the solid solutions or to coupling with electronic transitions in semiconductorsulfides.INTRODUCTIONRecently, particular effort was put intounderstanding the occurrence of sulfur-rich phases inmagmatic systems and meteorites as well as in materialscience and metallurgy (e.g., Sinyakavo and Kosyakov2001; Holzheid and Grove 2002; Keil 2007; Liu et al.2007). The degassing of sulfur from volcanoes plays animportant role in the present and past atmosphereproperties, and in the geochemical cycle of sulfur in theEarth system (e.g., Farquhar et al. 2002; Moretti andOttonello 2005; Liu et al. 2007). Sulfur can take a largenumber of oxidation states, from 2 to 6+, and itoccurs in several gaseous and crystallized forms.Because of this large range of possible oxidation states,it remains a difficult element to study.The sulfide compounds are important phases inmeteorites (e.g., Keil 1989, 2007). Specifically, the majorpart of sulfur in meteorites is found either in troilite;FeS; or in other sulfides like oldhamite, CaS,
TL;DR: Blithfield (EL6) is one of the known enstatite chondrite breccias as mentioned in this paper, which consists of troilite-rich clasts embedded in an extremely metallic Fe,Ni-rich matrix.