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1.
Amphibole + phlogopite + diopside bearing veins are observed in a large number of upper mantle xenoliths, but the composition of the melt that forms them is poorly constrained. Recent data from the Heldburg Phonolite, Central Germany, has shown that phonolite melt will react with olivine and orthopyroxene xenocrysts to form reaction rims of amphibole + phlogopite + diopside at mid-lower crustal pressures. This is the first example of where a melt has reacted with peridotite to form the mineralogy of the metasomatic veins. It is therefore necessary to explore whether a phonolite melt could be the parent melt that forms amphibole + phlogopite + diopside metasomatic veins. Experimental reactions between single crystals of olivine and orthopyroxene with phonolite melt were conducted at upper mantle conditions of 1.0–1.5 GPa and 900–1,000 °C. Melt water contents were varied from anhydrous to >12 wt. H2O. Olivine reacts to form phlogopite reaction rims with overgrowths of diopside <1,000 °C or rims of secondary olivine >1,000 °C. Orthopyroxene reacts to form amphibole with epitaxial diopside overgrowths <1,000 °C. No reaction rims form when the bulk melt H2O is lower than ~3.8 wt%. Pressure has little effect over the small range tested. These experiments reproduce reaction rims on olivine and orthopyroxene observed in the Heldburg Phonolite, Central Germany, and suggest that a relatively narrow range of temperatures and melt water contents is required for rim formation. The compositions of rim amphibole, phlogopite and diopside from the experiments have very similar compositions to those from Heldburg but do not match those from metasomatic veins. Phenocrysts from Heldburg are similar to the metasomatic veins, suggesting that a phonolite could potentially form the veins if vein formation is dominated by crystallization rather than reaction and replacement of wall rock phases. 相似文献
2.
Bridgmanite (Mg,Fe)SiO3 and ferropericlase (Mg,Fe)O are the most abundant phases in the lower mantle and localized regions of the D″ layer just above the core mantle boundary. Seismic anisotropy is observed near subduction zones at the top of the lower mantle and in the D″ region. One source of anisotropy is dislocation glide and associated texture (crystallographic preferred orientation) development. Thus, in order to interpret seismic anisotropy, it is important to understand texture development and slip system activities in bridgmanite and bridgmanite + ferropericlase aggregates. Here we report on in situ texture development in bridgmanite and bridgmanite + ferropericlase aggregates deformed in the diamond anvil cell up to 61 GPa. When bridgmanite is synthesized from enstatite, it exhibits a strong (4.2 m.r.d.) 001 transformation texture due to a structural relationship with the precursor enstatite phase. When bridgmanite + ferropericlase are synthesized from olivine or ringwoodite, bridgmanite exhibits a relatively weak 100 transformation texture (1.2 and 1.6 m.r.d., respectively). This is likely due to minimization of elastic strain energy as a result of Young’s modulus anisotropy. In bridgmanite, 001 deformation textures are observed at pressures <55 GPa. The 001 texture is likely due to slip on (001) planes in the [100], [010] and \(\left\langle {110} \right\rangle\) directions. Stress relaxation by laser annealing to 1500–1600 K does not result in a change in this texture type. However, at pressures >55 GPa a change in texture to a 100 maximum is observed, consistent with slip on the (100) plane. Ferropericlase, when deformed with bridgmanite, does not develop a coherent texture. This is likely due to strain heterogeneity within the softer ferropericlase grains. Thus, it is plausible that ferropericlase is not a significant source of anisotropy in the lower mantle. 相似文献
3.
The assemblage clinopyroxene + magnesite was observed in Earth’s high-pressure metamorphic samples, and its stability in subducting slabs was confirmed by experiments. Recent studies also suggested that the fO2 variations observed in SNC meteorites can be explained by polybaric graphite-CO-CO2 equilibria in the Martian mantle. Although there is no direct evidence for the stability of the cpx + mc assemblage in Mars mantle, its high-pressure–high-temperature decomposition to cpx + fo + CO2 makes it a good analogue for the source of carbon metasomatism, in particular, to study nakhlites formation. Iron, which is present in the Earth’s and Martian mantles, may, however, influence the speciation of carbon. We performed experiments on a clinopyroxene + magnesite assemblage at 1.8 and 3.0 GPa and temperatures corresponding to the Earth’s and Martian mantles. The role of iron and of fO2 was investigated by (1) replacing all or part of the magnesite by siderite FeCO3, (2) adding Fe0 and (3) using graphite C capsules. A carbonate-silicate melt forms at both Earth and Mars conditions. Clinopyroxene and olivine are the main solid phases in the iron-free experiments. Fe2+ and Fe0 decrease their melting temperatures and increase the silicate fraction in the melt. The produced carbonate-silicate melts may be involved in the formation of some carbon-rich lavas on Earth (e.g., carbonatites, ultramafic lamprophyres, or kamafugites). Our results may also be used to interpret ophiolite samples or inclusions. In particular, we show that wüstite may form in equilibrium with carbonate-silicate melt in opx-(and silica-) poor regions of the mantle below 3 GPa. Our results also confirm the hypothesis of carbon metasomatism in the Martian nakhlites source. Immiscibility or reduction could explain the absence or rarity of C in Martian lavas. 相似文献
4.
Numerical analysis of the groundwater regime in the western Dead Sea escarpment, Israel + West Bank 总被引：2，自引：2，他引：0
Agnes Gräbe Tino Rödiger Karsten Rink Thomas Fischer Feng Sun Wenqing Wang Christian Siebert Olaf Kolditz 《Environmental Earth Sciences》2013,69(2):571-585
Water is scarce in the semi-arid to arid regions around the Dead Sea, where water supply mostly relies on restricted groundwater resources. Due to increasing population in this region, the regional aquifer system is exposed to additional stress. This results in the continuous decrease in water level of the adjacent Dead Sea. The interaction of an increasing demand for water due to population growth and the decrease of groundwater resources will intensify in the near future. Thus, the water supply situation could worsen significantly unless sustainable water resource management is conducted. In this study, we develop a regional groundwater flow model of the eastern and southern Judea Group Aquifer to investigate the groundwater regime in the western Dead Sea drainage basin of Israel and the West Bank. An extensive geological database was developed and consequently a high-resolution structural model was derived. This structural model was the basis for various groundwater flow scenarios. The objective was to capture the spatial heterogeneity of the aquifer system and to apply these results to the southern part of the study area, which has not been studied in detail until now. As a result we analyzed quantitatively the flow regime, the groundwater mass balance and the hydraulic characteristics (hydraulic conductivity and hydraulic head) of the cretaceous aquifer system and calibrated them with PEST. The calibrated groundwater flow model can be used for integrated groundwater water management purposes in the Dead Sea area, especially within the framework of the SUMAR-Project. 相似文献
5.
C. R. L. Friend A. P. Nutman V. C. Bennett M. D. Norman 《Contributions to Mineralogy and Petrology》2008,155(2):229-246
Modern chemical sediments display a distinctive rare earth element + yttrium (REE + Y) pattern involving depleted LREE, positive
La/La*SN, Eu/Eu*SN, and YSN anomalies (SN = shale normalised) that is related to precipitation from circumneutral to high pH waters with solution complexation
of the REEs dominated by carbonate ions. This is often interpreted as reflecting precipitation from surface waters (usually
marine). The oldest broadly accepted chemical sediments are c. 3,700 Ma amphibolite facies banded iron-formation (BIF) units
in the Isua supracrustal belt, Greenland. Isua BIFs, including the BIF international reference material IF-G are generally
considered to be seawater precipitates, and display these REE + Y patterns (Bolhar et al. in Earth Planet Sci Lett 222:43–60,
2004). Greenland Eoarchaean BIF metamorphosed up to granulite facies from several localities in the vicinity of Akilia (island),
display REE + Y patterns identical to Isua BIF, consistent with an origin by chemical sedimentation from seawater and a paucity
of clastic input. Furthermore, the much-debated magnetite-bearing siliceous unit of “earliest life” rocks (sample G91/26)
from Akilia has the same REE + Y pattern. This suggests that sample G91/26 is also a chemical sediment, contrary to previous
assertions (Bolhar et al. in Earth Planet Sci Lett 222:43–60, 2004), and including suggestions that the Akilia unit containing G91/26 consists entirely of silica-penetrated, metasomatised,
mafic rock (Fedo and Whitehouse 2002a). Integration of our trace element data with those of Bolhar et al. (Earth Planet Sci Lett 222:43–60, 2004) demonstrates that Eoarchaean siliceous rocks in Greenland, with ages from 3.6 to 3.85 Ga, have diverse trace element signatures.
There are now geographically-dispersed, widespread examples with Isua BIF-like REE + Y signatures, that are interpreted as
chemically unaltered, albeit metamorphosed, chemical sediments. Other samples retain remnants of LREE depletion but are beginning
to lose the distinct La, Eu and Y positive anomalies and are interpreted as metasomatised chemical sediments. Finally there
are some siliceous samples with completely different trace element patterns that are interpreted as rocks of non-sedimentary
origin, and include metasomatised mafic rocks. The positive La/La*SN, Eu/Eu*SN and YSN anomalies found in Isua BIFs and other Eoarchaean Greenland samples, such as G91/26 from Akilia, suggests that the processes
of carbonate ion complexation controlling the REE − Y patterns were already established in the hydrosphere at the start of
the sedimentary record 3,600–3,850 Ma ago. This is in accord with the presence of Eoarchaean siderite-bearing marbles of sedimentary
origin, and suggests that CO2 may have been a significant greenhouse gas at that time. 相似文献
6.
Tsu-Chiang Lei Shiuan Wan Tien-Yin Chou Hung-Chieh Pai 《Environmental Earth Sciences》2011,63(5):981-997
Debris flow is often performed through identifying and analyzing the soil condition, hydraulic, geomorphological factors and
vegetation conditions. In the present study, a spatial information analysis system is combined with a linear statistical method
(principle components analysis with linear discriminant analysis, PCA + LDA) and an advanced data mining technique (discrete
rough sets, DRS) to investigate the debris flow occurrence based on geomorphological and vegetation conditions factors. The
analyzed data sources include (1) digital elevation model: to investigate the variation in the landscape, and (2) remote sensing
data: to analyze the vegetation and plant conditions on the ground surface. The objective of this research is to define a
method with the ability to forecast the level of debris flow susceptibility through the parallel study of statistical outcomes
(PCA + LDA) and data mining results (DRS). The outcomes from PCA + LDA are inadequate due to the thresholds of the influenced
variables not being examined. In this study, the DRS approach not only showed satisfactory results for the thresholds of influenced
variables in the study area, but also the occurrence rules of debris flow are generated. Finally, the results show superior
classification accuracy (70.8% for debris flow occurrence) for the DRS method over those of PCA + LDA analysis (54.2% for
debris flow occurrence) for the analysis of debris flow occurrence. Therefore, this is an encouraging preliminary approach
in the hazard assessment of debris flow. 相似文献
7.
K_2O-Al_2O_3-SiO_2-H_2O体系形成一些主要造岩矿物,如长石、石英和云母等,因此受到有关学者的广泛重视。为了探讨岩石的形成机制,国外许多学者曾研究过该体系矿物的稳定范围。近年来,伊万诺夫、J.W.谢德(Shade)、R.P.温特施(Wintsch)、D.M.伯特(Burt)、H.W.戴(Day)和J.J赫姆利(Hemley)等也先后用热力学方法研究过该体系的相平衡关系。但至今,该体系中某些矿物的相平衡关系仍然有争议,例如, 相似文献
8.
１金属基板上ＳｉＯ２ ＴｉＯ２ ＺｒＯ２陶瓷涂层工艺的研究现状在金属基板上进行Ｓｏｌ ｇｅｌ涂层是国外在９０年代发展起来的一项新工艺。根据金属陶瓷复合材料这一新兴工业的应用前景,一些工业发达国家的政府研究部门和工业界都十分重视这项新工艺的开发与研究,... 相似文献
11.
12.
本文用抽空石英管法对三元硫化物体系Ag_2S-Cu_2S-PbS和Ag_2S-Cu_2S-Bi_2S_3在500℃的相图进行了研究。 Ag_2S-Cu_2S-PbS体系500℃相关系,受方铅矿和固溶体f.c.c.(Ag_xCu_(2-x)S)、b.c.c.(Cu_xAg_(2-x)S)所控制。在接近PbS-Cu_2S连线处有一液相区。随温度下降,方铅矿可与Cu_2-Ag_2S二元系上所有各相平衡共存。 Ag_2S-Cu_2S-Bi_2S_3体系在500℃时则包含六个固溶体,即块硫铋银矿、铜银铅铋矿、杂硫铋银矿、硫铋铜矿、CuBi_3S_5、Cu_3Bi_5S_9和新合成“C”(Ag_(1.1)Cu_(4.8)Bi_(5.8)S_(12))。最令人感兴趣的是无铜、无铅的铜银铅铋矿(Ag_2Bi_4S_7)合成成功。 以上二个三元系中矿物稳定性及共生关系也根据相图研究结果进行了讨论。 相似文献
13.
M. Wildner 《Mineralogy and Petrology》1993,48(2-4):215-225
Summary Crystals of K2[Co2(SeO3)3]-2H2O and K2[Ni2(SeO3)3]-2H2O were synthesized under low-hydrothermal conditions. Their structures were determined using single crystal X-ray data up to sin / = 0.7Å-1. [Space group P63/m; a = 9.091(3),9.016(2)Å; c = 7.562(2), 7.476(2)Å; Z = 2; RW = 1.6, 2.5%]. The investigations confirmed that K2[Co2(SeO3)3].2H2O and K2[Ni2(SeO3)3]-2H2O represent the first selenites belonging to the zemannite structure type, a framework structure with wide channels running parallel [0001]. In both compounds four maxima were clearly located in the channel by Fourier summations and attributed to two K atoms and two H2O molecules, each with an occupancy factor of 1/6; a possible ordering scheme (full occupancy) with local symmetry 1 and [6]-coordinated K atoms could be derived for the channel atoms.Zusammenfassung Kristalle von K2[Co2(SeO3)3]-2H2O und K2[Ni2(SeO3)3]-2H2O wurden unter niedrig-hydrothermalen Bedingungen synthetisiert. Die Strukturen wurden unter Verwendung von Einkristallröntgendaten bis sin /= 0.7Å-1 bestimmt. [Raumgruppe P63/m; a = 9.091(3), 9.016(2)Å; c = 7.562(2), 7.476(2)Å; Z = 2; RW = 1.6, 2.5%] Die Untersuchungen bestätigten, daß K2[Co2(SeO3)3] - 2H2O und K2 [Ni2(SeO3)3] - 2H2O als erste Selenite dem Strukturtyp des Zemannits angehören, einer Gerüststruktur mit weiten, parallel [0001] verlaufenden Kanälen. In beiden Verbindungen wurden im Kanal vier Maxima durch Fourier-Summationen eindeutig lokalisiert und zwei Kalium-atomen sowie zwei H2O Molekülen, jeweils mit einem Besetzungsfaktor von 1/6, zugeschrieben. Für die Kanalatome konnte ein möglicher Ordnungszustand (volle Besetzung) mit lokaler Symmetrie 1 und [6]-koordinierten Kaliumatomen abgeleitet werden.
Dedicated to Prof. Dr. Josef Zemann at the occasion of his 70th birthday
With 2 Figures 相似文献
Selenite des Zemannittyps: Kristallstrukturen von K2[Co2(SeO3)3] - 2H2O und K2[Ni2(SeO3)3]-2H2O
Dedicated to Prof. Dr. Josef Zemann at the occasion of his 70th birthday
With 2 Figures 相似文献
14.
15.
V. G. Thomas S. Z. Smirnov O. A. Kozmenko V. A. Drebushchak V. S. Kamenetsky 《Petrology》2014,22(3):293-309
In order to determine the mechanisms of formation and properties of natural hydrosilicate liquids (HSLs), which are formed during the transition from magmatic to hydrothermal mineral formation in granitic pegmatites and rare-metal granites, the formation of HSLs was experimentally studied in the Na2O-SiO2-H2O, Na2O-Al2O3-SiO2-H2O, and Na2O-K2O-Li2O-Al2O3-SiO2-H2O systems at 600°C and 1.5 kbar. It was shown that the sequential extension of composition does not suppress HSL formation in the systems and expands the stability field of this phase. However, HSLs formed in extended chemical systems have different structure and properties: the addition of alumina induces some compression of the structure of the silicate framework of HSLs, which results in a decrease in water content in this phase and probably hinders the reversibility of its dehydration. It was demonstrated that HSL can be formed by the coagulation of silica present in a silica-oversaturated alkaline aqueous fluid. It was supposed that the HSL formed during this process has a finely dispersed structure. It was argued that anomalous enrichment in some elements in natural HSLs can be due to their sorption by the extensively developed surface of HSL at the moment of its formation. 相似文献
16.
离子色谱法测定水样中S2-、SO2-3、SO2-4、S2O2-3 总被引：1，自引：0，他引：1
该种方法利用离子色谱仪的电导检测器与电化学检测器串联,十几分钟即可连续完成水中S2-、SO2-3、SO2-4、S2O2-3的测定,方法具有快速、高效、方便、灵敏、选择性好等特点.方法的检出限分别为S2-12.5μg/L;SO2-3 22.4μg/L;SO2-4 5.0μg/L;S2O2-3 5.0μg/L.相对标准偏差在1.5%～6.9%之间,能够满足水中S2-、SO2-3、SO2-4、S2O2-3四种阴离子分析测试的需要. 相似文献
17.
为了计算高温，高压和高密度流体的热力学性质，提出了一个具有19个参数的维里型状态方程，其中参数与温度间的函数关系采用由Sutherland位能函数导出的维里系数近似式。除临界点附近以外，在已报道的pVT数据所覆盖的大部分超临界区域内，该方程均可适用。用该方程对H2O，CH4，H2，CO2，CO和O2等流体pVT关系的计算结果令人满意，其中pVT上限分别为：91-610GPa,1.6-11.0cm^3/mol,4000-5000K。计算体积的平均偏 小于0．8％，最大偏差小于5．4％。 相似文献
18.
Polarized single crystal absorption spectra, in the spectral range 40 000–5 000 cm-1, were obtained on Co2+ in trigonally distorted octahedral oxygen fields of buetschliite-type K2Co(SeO3)2 (I), K2Co2(SeO3)3 (II) and zemannite-type K2Co2(SeO3)3 · 2H2O (III). Site symmetries of Co2+ are
m (D3d) in I, 3m (C3v) in II, and 3 (C3) in III. The spectra can be interpreted on the basis of an electric dipole mechanism, wherein transitions of Co2+ in the centrosymmetric site in I gain intensity from dynamic removal of the inversion centre by vibronic coupling. In accordance with the elongation of the CoO6 octahedra along the trigonal axis, the split component E(g) of the ground state 4T1g in octahedral fields is the ground state in all three compounds. Trigonal field parameters Dq(trig), D, D and the Racah parameters B have been fitted to the energies of spin allowed transitions (293 K) as follows: I: 744, 94, -16, and 838 cm-1, resp.; II: 647, 227, 42, and 798 cm-1, resp.; III: 667, 181, 21, and 809 cm-1, respectively. Racah parameters C were estimated from the energy of some observed spin-forbidden transitions to be 3770 (I), 3280 (II), and 3465 cm-1 (III). Values of Dq and of the Racah parameters B and C indicate slight differences of Co2+-O bonding in I as compared to II and III, with somewhat higher covalency in compounds II and III which contain face-sharing CoO6 octahedra with short Co-Co contacts. Also, in II and III the observed D values do not agree with theoretical D values, predicted from the magnitude of the mean octahedral distortions. 相似文献
19.
吕明1，2，汤良杰1，2 总被引：1，自引：0，他引：1
通过系统的地震资料综合解释,对塔里木盆地巴楚隆起卡拉沙依断裂上、下盘沉积地层厚度的变化及各界面与上、下部地层的接触关系、不整合面的发育特征及变化规律进行研究,以此来探讨卡拉沙依断裂各时期的活动特征。认为卡拉沙依断裂东、西两段呈现出截然不同的活动特征。主断裂东段,晚寒武世-奥陶纪,断裂无明显活动;早志留世晚期-早二叠世,断裂开始活动,呈现出逆冲推覆断裂的特征;经中二叠世的平静期,从晚二叠世开始又有一次逆冲推覆活动。而位于主断裂南侧的次级断裂,在晚寒武纪-中志留世,断裂无明显活动;从早中泥盆世开始,次级断裂开始活动,表现为压性断裂特征,逆冲推覆作用持续至早二叠世,经过中二叠世短暂的平静期,在晚二叠世还有一次继承性活动,但活动强度较弱。主断裂西段,奥陶纪时期,断裂开始活动并表现出张性断裂活动特征;经过志留纪-中二叠世的平静期,从晚二叠世开始,断裂西段发生正反转作用,逆冲推覆活动明显。次级断裂西段,在晚寒武世-早中二叠世并无活动,从晚二叠世开始,断裂开始活动,表现为强烈的逆冲推覆作用。 相似文献