硅藻土中水的NMR研究   总被引：2，自引：0，他引：2  

李新安  张惠芬  冯璜  罗立峰  王辅亚  魏惠芳 《矿物学报》1999,19(2):154-160

本文用ＮＭＲ技术研究硅藻土中水的存在状态和特征及灼烧条件下的脱水和室温大气下的重吸水过程。样品包括一个宝石级单矿物蛋白石和采自雷州半岛地区的海康卜昌和徐闻九亩的硅藻土地表样和它们经不同温度自理后的产物。  相似文献   

Subduction metamorphism of serpentinite‐hosted carbonates beyond antigorite‐serpentinite dehydration (Nevado‐Filábride Complex,Spain)     

Manuel D. Menzel  Carlos J. Garrido  Vicente Lpez Snchez‐Vizcaíno  Kroly Hidas  Claudio Marchesi 《Journal of Metamorphic Geology》2019,37(5):681-715

At sub‐arc depths, the release of carbon from subducting slab lithologies is mostly controlled by fluid released by devolatilization reactions such as dehydration of antigorite (Atg‐) serpentinite to prograde peridotite. Here we investigate carbonate–silicate rocks hosted in Atg‐serpentinite and prograde chlorite (Chl‐) harzburgite in the Milagrosa and Almirez ultramafic massifs of the palaeo‐subducted Nevado‐Filábride Complex (NFC, Betic Cordillera, S. Spain). These massifs provide a unique opportunity to study the stability of carbonate during subduction metamorphism at P–T conditions before and after the dehydration of Atg‐serpentinite in a warm subduction setting. In the Milagrosa massif, carbonate–silicate rocks occur as lenses of Ti‐clinohumite–diopside–calcite marbles, diopside–dolomite marbles and antigorite–diopside–dolomite rocks hosted in clinopyroxene‐bearing Atg‐serpentinite. In Almirez, carbonate–silicate rocks are hosted in Chl‐harzburgite and show a high‐grade assemblage composed of olivine, Ti‐clinohumite, diopside, chlorite, dolomite, calcite, Cr‐bearing magnetite, pentlandite and rare aragonite inclusions. These NFC carbonate–silicate rocks have variable CaO and CO₂ contents at nearly constant Mg/Si ratio and high Ni and Cr contents, indicating that their protoliths were variable mixtures of serpentine and Ca‐carbonate (i.e., ophicarbonates). Thermodynamic modelling shows that the carbonate–silicate rocks attained peak metamorphic conditions similar to those of their host serpentinite (Milagrosa massif; 550–600°C and 1.0–1.4 GPa) and Chl‐harzburgite (Almirez massif; 1.7–1.9 GPa and 680°C). Microstructures, mineral chemistry and phase relations indicate that the hybrid carbonate–silicate bulk rock compositions formed before prograde metamorphism, likely during seawater hydrothermal alteration, and subsequently underwent subduction metamorphism. In the CaO–MgO–SiO₂ ternary, these processes resulted in a compositional variability of NFC serpentinite‐hosted carbonate–silicate rocks along the serpentine‐calcite mixing trend, similar to that observed in serpentinite‐hosted carbonate‐rocks in other palaeo‐subducted metamorphic terranes. Thermodynamic modelling using classical models of binary H₂O–CO₂ fluids shows that the compositional variability along this binary determines the temperature of the main devolatilization reactions, the fluid composition and the mineral assemblages of reaction products during prograde subduction metamorphism. Thermodynamic modelling considering electrolytic fluids reveals that H₂O and molecular CO₂ are the main fluid species and charged carbon‐bearing species occur only in minor amounts in equilibrium with carbonate–silicate rocks in warm subduction settings. Consequently, accounting for electrolytic fluids at these conditions slightly increases the solubility of carbon in the fluids compared with predictions by classical binary H₂O–CO₂ fluids, but does not affect the topology of phase relations in serpentinite‐hosted carbonate‐rocks. Phase relations, mineral composition and assemblages of Milagrosa and Almirez (meta)‐serpentinite‐hosted carbonate–silicate rocks are consistent with local equilibrium between an infiltrating fluid and the bulk rock composition and indicate a limited role of infiltration‐driven decarbonation. Our study shows natural evidence for the preservation of carbonates in serpentinite‐hosted carbonate–silicate rocks beyond the Atg‐serpentinite breakdown at sub‐arc depths, demonstrating that carbon can be recycled into the deep mantle.  相似文献   

Dehydration melting of micas in the Chilka Lake Khondalites: The link between the metapelites and granitoids     

S. K. Sen  S. Bhattacharya 《Journal of Earth System Science》1997,106(4):277-297

Garnet-sillimanite gneisses, locally known as khondalites, occur abundantly in the Chilka Lake granulite terrane belonging to the Eastern Ghats Proterozoic belt of India. Though their chemistry has been modified by partial melting, it is evident that the majority of these rocks are metapelitic, with some tending to be metapsammitic. Five petrographically distinct groups are present within the khondalites of which the most abundant group is characteristically low in Mg:Fe ratios — the main chemical discriminant separating the five groups. The variations in Mg:Fe ratios of the garnets, biotites, cordierites, orthopyroxenes and spinels from the metapelites are compatible with those in the bulk rocks. A suite of granitoids containing garnet, K-feldspar, plagioclase and quartz, commonly referred to as leptynites in Indian granulite terranes, are interlayered with khondalites on the scale of exposures; in a few spots, the intercalated layers are thin. The peraluminous character of the leptynites and presence of sillimanite trails within garnets in some of them suggest derivation of leptynites by partial melting of khondalites. Here we examine this connection in the light of results derived from dehydration melting experiments of micas in pelitic and psammitic rocks. The plots of leptynites of different chemical compositions in a (MgO + FeO)-Na₂O-K₂O projection match the composition of liquids derived by biotite and muscovite dehydration melting, when corrected for co-products of melting reactions constrained by mass balance and modal considerations. The melt components of the leptynites describe four clusters in the M-N-K diagram. One of them matches melts produced dominantly by muscovite dehydration melting, while three clusters correspond to melting of biotite. The relative disposition of the clusters suggests two trends, which can be correlated with different paths that pelitic and psammitic protoliths are expected to generate during dehydration melting. Thus the leptynites evidently represent granitoids which were produced by dehydration melting in metapelites of different compositions. The contents of Ti, Y, Nb, Zr and Th in several leptynites indicate departures from equilibrium melt compositions, and entrainment of restites is considered to be the main causative factor. Disequilibrium in terms of major elements is illustrated by leucosomes within migmatites developed in a group of metapelites. But the discrete leptynites that have been compared with experimental melts approach equilibrium melt compositions closely.  相似文献   

Inducing action of hydrogen migrating along faults on earthquakes     

Qichu Su  E. Zeller  E. Angino 《地震学报(英文版)》1992,5(4):841-847

The reduction of the microhardness and the crystal constants of some non-metallic materials, such as calcite, dolomite, antigorite, etc., are observed after a short time of hydrogen permeating treatment at low pressure. It means that hydrogen diffusion can cause their strength dropping or weakening. The hydrogen, which is produced under the earth by various chemical reactions or accumulated when the earth formed, is migrating up continuously along faults, causing weakening of rocks and faults at the same time. So it is possible that rocks and faults break under lower tectonic stress condition. Hydrogen anomalies are passive reflection, precursor and accompaniment of fault activities or earthquakes on the face of it, but hydrogen migrating has active influence on faults and its moving. The Chinese version of this paper appeared in the Chinese edition ofActa Seismologica Sinica,14, 229–235, 1992.  相似文献   

Dehydration of metapelites during high‐P metamorphism: The coupling between fluid sources and fluid sinks          下载免费PDF全文

Simon Schorn 《Journal of Metamorphic Geology》2018,36(3):369-391

Polymetamorphic metapelites and embedded eclogites share a complex, episodic interplay of dehydration and fluid infiltration at the eclogite type‐locality (Saualpe–Koralpe, Eastern Alps, Austria). The metapelites inherited a fluid content (i.e. mineral‐bound OH expressed in terms of mol.% H₂O) of ～6–7 mol.% H₂O from high‐T–low‐P metamorphism experienced during the Permian. At or near P_max of the subsequent Eoalpine event (～20 kbar and 680^°C), the breakdown of paragonite to Na‐rich clinopyroxene and kyanite in metapelites released a discrete pulse of hydrous fluid. Prior to the dehydration event, the rocks were largely fluid absent, allowing only limited re‐equilibration during the prograde Eoalpine evolution. Similarly, Permian‐aged gabbros have persisted metastably due to the absence of a catalyst prior to fluid‐induced re‐equilibration. The fluid triggered partial to complete eclogitization along a fluid infiltration front partially preserved in metagabbro. Near‐isothermal decompression to ～7.5–10 kbar and 670–690°C took place under fluid‐absent conditions. After decompression, a second breakdown of phengitic white mica and garnet produced muscovite, biotite, plagioclase and ～0.1–0.7 mol.% H₂O that enhanced extensive fluid‐aided re‐equilibration of the metapelites. Potential relicts of high‐P assemblages were largely obliterated and replaced by the recurrent amphibolite facies assemblage garnet+biotite+staurolite+kyanite+muscovite+plagioclase+ilmenite+quartz. The hydrous fluid originating from the metapelites infiltrated the embedded eclogites at these P–T conditions and induced the local breakdown of the peak assemblage omphacite and garnet to fine‐grained symplectites of diopside and plagioclase. Further fluid infiltration led to the formation of hornblende–quartz poikiloblasts at the expense of the symplectites. The metapelites re‐equilibrated until the growth of retrograde staurolite consumed any remaining free fluid, thereby terminating the process. Further re‐equilibration is inhibited by both the lack of a catalytic fluid and H₂O as a reactant essential for rehydration reactions. The interplay between fluid sources and fluid sinks describes a closed cycle for the rocks at the eclogite type‐locality. Final, near‐isobaric cooling is indicated by a slight increase of X_Fe in garnet rims. Post‐decompression dehydration and fluid‐aided re‐equilibration arrested by the introduction of staurolite might explain the apparently homogeneous retrogression conditions as well as the notorious absence of diagnostic high‐P assemblages in metapelites at the eclogite type‐locality.  相似文献   

角闪石高温高压实验研究进展及其地球物理意义     

韩珂楠  易丽  王多君  刘川江  张瑞鑫 《吉林大学学报(地球科学版)》2022,52(2):486-502

高温高压实验作为地球科学研究的重要方向之一,通过模拟地球深部的温度和压力条件,了解地球深部物质的物理化学性质、地球内部结构和动力学演化。角闪石属于双链硅酸盐矿物,为地幔岩石圈的重要组成,广泛分布在海洋地壳、俯冲板块、变质岩和火成岩中。作为俯冲带的重要含水矿物,角闪石的广泛分布和高温高压下的脱水对于理解俯冲带水含量以及水迁移具有重要作用,同时在俯冲带的地震活动、高电导率异常、地震波速异常和岩浆活动中扮演重要角色。在过去的近百年时间里,国内外学者对角闪石高温高压物理化学性质进行了大量的研究。角闪石具有非常复杂的元素组成和结构特征,由此也导致了不同角闪石物理化学性质存在显著不同,包括脱水与脱羟基反应中元素迁移的差异、角闪石形成与分解过程中碱性元素(K+Na)和H2O含量对热稳定的影响、不同空间群结构下的高压结构相变、原位条件下不同结晶方向的电导率异常、不同结晶学优选方位(CPO)下的波速异常等。已有的研究对于角闪石的物理化学性质以及其在俯冲带中发挥的作用有了比较清楚的认识,但仍然有许多问题需要进一步研究,如角闪石的高压脱水动力学、热物性和变形机制等。  相似文献   

Arrested charnockite formation at Kottavattam, southern India   总被引：7，自引：0，他引：7  

M. RAITH  C. SRIKANTAPPA 《Journal of Metamorphic Geology》1993,11(6):815-832

Abstract At Kottavattam, southern Kerala (India), late Proterozoic homogeneous leptynitic garnet–biotite gneisses of granitic composition have been transformed on a decimetric scale into coarse-grained massive charnockite sensu stricto along a set of conjugate fractures transecting the gneissic foliation. Charnockitization post-dates the polyphase deformation, regional high-grade metamorphism and anatexis, and evidently occurred at a late stage of the Pan-African tectonothermal history. Geothermobarometric and fluid inclusion data document textural and chemical equilibration of the gneiss and charnockite assemblages at similar P_lith–T conditions (650–700°C, 5–6 kbar) in the presence of carbonic fluids internally buffered by reaction with graphite and opaque mineral phases (X_CO2= 0.7–0.6; X_H2O= 0.2–0.3; X_N2= 0.1; log f_O2= -17.5). Mineralogical zonation indicates that charnockitization of the leptynitic gneiss involved first the breakdown of biotite and oxidation of graphite in narrow, outward-migrating transition zones adjacent to the gneiss, followed by the breakdown of garnet and the neoblastesis of hypersthene in the central charnockite zone. Compared to the host gneiss, the charnockite shows higher concentrations of K, Na, Sr, Ba and Zn and lower concentrations of Mg, Fe, Ti, V, Y, Zr and the HREE, with a complementary pattern in the narrow transition zones of biotite breakdown. The P_lith–T–X_H2O data and chemical zonation patterns indicate charnockitization through subsolidus-dehydration reaction in an open system. Subsequent residence of the carbonic fluids in the charnockite resulted in low-grade alteration causing modification of the syn-charnockitic elemental distribution patterns and the properties of entrapped fluids. We favour an internally controlled process of arrested charnockitization in which, during near-isothermal uplift, the release of carbonic fluids from decrepitating inclusions in the host gneiss into simultaneously developing fracture zones led to a change in the fluid regime from ‘fluid-absent’in the gneiss to ‘fluid-present’in the fracture zones and to the development of an initial fluid-pressure gradient, triggering the dehydration reaction.  相似文献   

The fate of B, Cl and Li in the subducted oceanic mantle and in the antigorite breakdown fluids   总被引：2，自引：0，他引：2  

Marco Scambelluri  Othmar Müntener  Thomas T Pettke 《Earth and Planetary Science Letters》2004,222(1):217-234

We present an inventory of B, Cl and Li concentrations in (a) key minerals from a set of ultramafic samples featuring the main evolutionary stages encountered by the subducted oceanic mantle, and in (b) fluid inclusions produced during high-pressure breakdown of antigorite serpentinite. Samples correspond to (i) nonsubducted serpentinites (Northern Apennine and Alpine ophiolites), (ii) high-pressure olivine-bearing antigorite serpentinites (Western Alps and Betic Cordillera), (iii) high-pressure olivine-orthopyroxene rocks recording the subduction breakdown of antigorite serpentinites (Betic Cordillera). Two main dehydration episodes are recorded by the sample suite: partial serpentinite dewatering during formation of metamorphic olivine, followed by full breakdown of antigorite serpentine to olivine+orthopyroxene+fluid. Ion probe and laser ablation ICP-MS (LA ICP-MS) analyses of Cl, B and Li in the rock-forming minerals indicate that the hydrous mantle is an important carrier of light elements. The estimated bulk-rock B and Cl concentrations progressively decrease from oceanic serpentinites (46.7 ppm B and 729 ppm Cl) to antigorite serpentinites (20 ppm B and 221 ppm Cl) to olivine-orthopyroxene rocks (9.4 ppm B and 45 ppm Cl). This suggests release of oceanic Cl and B in subduction fluids, apparently without inputs from external sources. Lithium is less abundant in oceanic serpentinites (1.3 ppm) and the initial concentrations are still preserved in high-pressure antigorite serpentinites. Higher Li contents in olivine, Ti-clinohumite of the olivine-orthopyroxene rocks (4.9 ppm bulk rock Li), as well as in the coexisting fluid inclusions, suggest that their budget may not be uniquely related to recycling of oceanic Li, but may require input from external sources.Laser ablation ICP-MS analyses of fluid inclusions in the olivine-orthopyroxene rocks enabled an estimate of the Li and B concentrations in the antigorite breakdown fluid. The inclusion compositions were quantified using a range of salinity values (0.4-2 wt.% NaCl_equiv) as internal standards, yielding maximum average ^fluid/rockD_B∼5 and ^fluid/rockD_Li∼3.5. We also performed model calculations to estimate the B and Cl loss during the two dehydration episodes of serpentinite subduction. The first event is characterized by high fluid/rock partition coefficients for Cl (∼100) and B (∼60) and by formation of a fluid with salinity of 4-8 wt.% NaCl_equiv. The antigorite breakdown produces less saline fluids (0.4-2 wt.% NaCl_equiv) and is characterized by lower partition coefficients for Cl (25-60) and B (12-30). Our calculations indicate that the salinity of the subduction fluids decreases with increasing depths. ^fluid/rockD_B/^fluid/rockD_Cl<1 (∼0.5) indicates that Cl preferentially partitions into the evolved fluids relative to B and that the B/Cl of fluids progressively increases with increasing depths and temperatures.Despite light element release in fluids, appreciable B, Cl and Li are still retained in chlorite, olivine and Ti-clinohumite beyond the antigorite stability field. This permits a bulk storage of about 10 ppm B, 45 ppm Cl and 5 ppm Li, i.e., concentrations much higher than in mantle reservoirs. Chlorite is the Cl repository and its stability controls the Cl and H₂O budget beyond the antigorite stability; B and Li are bound in olivine and clinohumite. The subducted oceanic mantle thus retains light elements beyond the depths of arc magma sources, potentially introducing anomalies in the upper mantle.  相似文献   

Estimation of land subsidence caused by loss of smectite-interlayer water in shallow aquifer systems     

Chen-Wuing Liu  Wen-Sheng Lin  Li-Hsin Cheng 《Hydrogeology Journal》2006,14(4):508-525

Traditionally, land subsidence that results from groundwater over-pumping has often been described by the theory of consolidation. The mechanism of land subsidence due to the dehydration of clay minerals is not well addressed. A model of the “hydration state of smectite”, and a “solid solution model of smectite dehydration”, incorporating a thermodynamic solid solution model and laboratory results concerning clay-water systems of swelling pressure, hydration state and basal spacing in smectite interlayer, are employed to examine the effect of the release of water from the smectite interlayer on land subsidence in the coastal area of the Chou-Shui River alluvial fan and the Yun Lin offshore industrial infrastructure complex in Taiwan. The results indicate that 9.56–22.80% of the total cumulative land subsidence to a depth of 300 m is consistent with smectite dehydration following the over-pumping of groundwater. This dehydration-related land subsidence occurred to a depth of 0–60 m, with subsidence due to smectite dehydration accounting for 6.20–13.32% of the primary consolidation. Additionally, the total amount of subsidence resulting from both smectite dehydration and primary consolidation is consistent with the subsidence observed in the field. This study reveals that smectite dehydration appears to be important in assessing and predicting land subsidence in shallow aquifer systems.  相似文献   

The Role of Advective Fluid Flow and Diffusion during Localized, Solid-State Dehydration: Sondrum Stenhuggeriet, Halmstad, SW Sweden     

HARLOV  DANIEL E.; JOHANSSON  LEIF; VAN DEN KERKHOF  ALFONS; FORSTER  HANS-JURGEN 《Journal of Petrology》2006,47(1):3-33

A localized dehydration zone, Söndrum stone quarry, Halmstad,SW Sweden, consists of a central, 1 m wide granitic pegmatoiddyke, on either side of which extends a 2·5–3 mwide dehydration zone (650–700°C; 800 MPa; orthopyroxene–clinopyroxene–biotite–amphibole–garnet)overprinting a local migmatized granitic gneiss (amphibole–biotite–garnet).Whole-rock chemistry indicates that dehydration of the graniticgneiss was predominantly isochemical. Exceptions include [Y+ heavy rare earth elements (HREE)], Ba, Sr, and F, which aremarkedly depleted throughout the dehydration zone. Systematictrends in the silicate and fluorapatite mineral chemistry acrossthe dehydration zone include depletion in Fe, (Y + HREE), Na,K, F, and Cl, and enrichment in Mg, Mn, Ca, and Ti. Fluid inclusionchemistry is similar in all three zones and indicates the presenceof a fluid containing CO₂, NaCl, and H₂O components. Water activitiesin the dehydration zone average 0·36, or X_H2O = 0·25.All lines of evidence suggest that the formation of the dehydrationzone was due to advective transport of a CO₂-rich fluid witha minor NaCl brine component originating from a tectonic fracture.Fluid infiltration resulted in the localized partial breakdownof biotite and amphiboles to pyroxenes releasing Ti and Ca,which were partitioned into the remaining biotite and amphibole,as well as uniform depletion in (Y + HREE), Ba, Sr, Cl, andF. At some later stage, H₂O-rich fluids (H₂O activity >0·8)gave rise to localized partial melting and the probable injectionof a granitic melt into the tectonic fracture, which resultedin the biotite and amphibole recording a diffusion profile forF across the dehydration zone into the granitic gneiss as wellas a diffusion profile in Fe, Mn, and Mg for all Fe–Mgsilicate minerals within 100 cm of the pegmatoid dyke. KEY WORDS: charnockite; fluids; CO₂; brines; localized dehydration; Söndrum  相似文献