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Ultrahigh pressure macro diamonds from Copeton (New South Wales, Australia), based on Raman spectroscopy of inclusions 总被引：1，自引：0，他引：1
Mining of Cenozoic alluvial deposits at Copeton and Bingara (Eastern Australia) has produced two million macrodiamonds (0.25 ct median size). Raman spectroscopy is used to identify included minerals within uncut Copeton diamonds, with sealed chamber remnant pressures of 31.7 to 35.6 kbar for coesite, 13.6 and 22.7 kbar for clinopyroxene, and 7.6 kbar for grossular garnet. Assuming elastic behaviour, these values generate inclusion entrapment PT loci which intersect, restricting diamond formation conditions: from 250 °C, 43 kbar to 800 °C, 52 kbar. Larger than error (± 100 °C and ± 4 kbar), this range shows a systematic variation in inclusion composition with diamond zoning and N properties. Published research shows 1) Copeton and Bingara diamonds are unique, and 2) modern alluvium in the Bingara district carries mantle-formed garnet, captured by post-tectonic alkali basalt from an extensive diamondiferous ultrahigh pressure (UHP) terrane that stalled at depth because it is dominated by mafic eclogite. The combined Raman and geological results indicate two sets of subduction UHP diamond formation conditions/protolith are required, firstly cooler oceanic slab and secondly including higher temperature continental crust. The Copeton and Bingara stones are UHP macrodiamonds, and Carboniferous 40Ar/39Ar age dates on clinopyroxene inclusions should be interpreted as ages of crystallisation, representing the termination of subduction. The characteristic features of ruptured inclusions and etched percussion marks on Copeton and Bingara diamond indicate volcanic delivery to the earth's surface. Alluvial deposits elsewhere in Eastern Australia may carry similar diamond along with diamond of different origin. 相似文献
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利用矿物内部一致性热力学数据，建立了在ＣａＯ－Ａｌ２Ｏ３－ＭｇＯ－ＳｉＯ２－Ｈ２Ｏ体系中含钙铝榴石的葡萄石－绿纤石变质相平衡，确立了在葡萄石－绿纤石－钙铝榴石－绿帘石－绿泥石－石英组合中出现绿纤石－钙铝榴石共生、葡萄石－绿纤石共生、葡萄石－绿帘石共生和绿泥石－绿帘石－钙铝榴石共生的ＰＴ区间及其意义。根据该相平衡计算了新疆萨尔托海蛇绿岩中变基性岩石的葡萄石－绿纤石相变质ＰＴ条件为Ｔ＝３２５℃～３３５℃，Ｐ＝０．４５～０．４７５ＧＰａ。并讨论了Ｆｅ３＋＝Ａｌ替代对于形成钙铝榴石－绿纤石共生的影响。本文的研究表明，葡萄石－绿纤石－钙铝榴石－绿帘石－绿泥石－石英共生组合是葡萄石－绿纤石相中偏高压组合，钙铝榴石－绿纤石共生与绿纤石－阳起石相一样代表着葡萄石－绿纤石相中较高压相，钙铝榴石在葡萄石－绿纤石相中是可以稳定存在的。 相似文献
3.
S. Quartieri G. Antonioli C. A. Geiger G. Artioli P. P. Lottici 《Physics and Chemistry of Minerals》1999,26(3):251-256
The incorporation and site preference of minor amounts (about 1 wt%) of Yb3+ in synthetic pyrope (Mg3Al2Si3O12) and grossular (Ca3Al2Si3O12) garnet were studied by X-ray Absorption Fine-Structure (XAFS) Spectroscopy. The measurements, performed in the temperature
range 77–343 K at both Yb LI- and LIII-edges, demonstrate that Yb3+ enters the garnet structure and is located in the dodecahedral site in both samples. The coordination environment of Yb3+ in the two samples was compared to that of the X-site cation in end-member synthetic pyrope and grossular and in Yb3Al5O12 as determined by single-crystal X-ray diffraction. The local geometry around Yb3+ is different from that of Mg and Ca in the bulk of the garnet, and also from that of Yb3+ in Yb3Al5O12.
Τhe XAFS results indicate that, (1) structural relaxation occurs around Yb3+ in the garnet structure; (2) the host garnet matrix exerts a major structural control on the incorporation of Yb3+, and (3) minor amounts of Yb3+ in garnet are located in structural sites and not in ill-defined defects.
Received: 15 January 1998/ Revised, accepted: 21 July 1998 相似文献
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A. Pavese V. Diella V. Pischedda M. Merli R. Bocchio M. Mezouar 《Physics and Chemistry of Minerals》2001,28(4):242-248
The thermoelastic parameters of natural andradite and grossular have been investigated by high-pressure and -temperature
synchrotron X-ray powder diffraction, at ESRF, on the ID30 beamline. The P–V–T data have been fitted by Birch-Murnaghan-like EOSs, using both the approximated and the general form. We have obtained for
andradite K
0=158.0(±1.5) GPa, (dK/dT )0=−0.020(3) GPa K−1 and α0=31.6(2) 10−6 K−1, and for grossular K
0=168.2(±1.7) GPa, (dK/dT)0=−0.016(3) GPa K−1 and α0=27.8(2) 10−6 K−1. Comparisons between the present issues and thermoelastic properties of garnets earlier determined are carried out.
Received: 7 July 2000 / Accepted: 20 October 2000 相似文献
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In order to clarify Al2O3 content and phase stability of aluminous CaSiO3-perovskite, high-pressure and high-temperature transformations of Ca3Al2Si3O12 garnet (grossular) were studied using a MA8-type high-pressure apparatus combined with synchrotron radiation. Recovered samples
were examined by analytical transmission electron microscopy. At pressures of 23–25 GPa and temperatures of 1000–1600 K, grossular
garnet decomposed into a mixture of aluminum-bearing Ca-perovskite and corundum, although a metastable perovskite with grossular
composition was formed when the heating duration was not long enough at 1000 K. On release of pressure, this aluminum-bearing
CaSiO3-perovskite transformed to the “LiNbO3-type phase” and/or amorphous phase depending on its Al2O3 content. The structure of this LiNbO3-type phase is very similar to that of LiNbO3 but is not identical. CaSiO3-perovskite with 8 to 25 mol% Al2O3 was quenched to alternating lamellae of amorphous layer and LiNbO3-type phase. On the other hand, a quenched product from CaSiO3-perovskite with less than 6 mol% consisted only of amorphous phase. Most of the inconsistencies amongst previous studies
could be explained by the formation of perovskite with grossular composition, amorphous phase, and the LiNbO3-type phase.
Received: 11 April 2001 / Accepted: 5 July 2002 相似文献
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