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1.
Trace amount of water associated with the lattice defects of nominally anhydrous minerals (NAMs) can be measured using Fourier transform infrared spectroscopy (FTIR) and secondary ion mass spectrometry (SIMS). Lots of data on water in NAMs from different lithologies, especially mantle peridotite xenoliths, have been published. The water distribution in olivine from peridotite xenoliths often displays a diffusion profile with high water concentration in the core and low at the rim, which indicates water loss via diffusion during the ascent of host magma. On the other hand, water is homogeneously distributed in pyroxene and its concentration is typically interpreted to represent a mantle value. The water concentration of magma in equilibrium with NAM can be estimated using specific partition coefficient, from which the water content of parental magma and the mantle source can be inferred. The accuracy of this method, however, depends on the selection of appropriate partition coefficient for the system. Using hydrogen isotope compositions and H2O/Ce ratios of mantle NAMs, water source regions can be traced and water heterogeneity can be mapped in the upper mantle. Water plays an important role in the stability of cratonic mantle. The water contents and vertical distribution patterns can be significantly different among different cratonic mantles, which may result from different geologic activities. However, the mantle-plume interaction may not necessarily result in significant change of water content in cratonic mantle. The estimation of the water content in the upper mantle is still largely based on geochemical models due to the limitations of data on water in mantle NAMs.  相似文献   

2.
Magnetotelluric (MT) data can image the electrical resistivity of the entire lithospheric column and are therefore one of the most important data sources for understanding the structure, composition and evolution of the lithosphere. However, interpretations of MT data from stable lithosphere are often ambiguous. Recent results from mineral physics studies show that, from the mid-crust to the base of the lithosphere, temperature and the hydrogen content of nominally anhydrous minerals are the two most important controls on electrical conductivity. Graphite films on mineral grain boundaries also enhance conductivity but are stable only to the uppermost mantle. The thermal profile of most stable lithosphere can be well constrained, so the two important unknowns that can affect the conductivity of a lithospheric section are hydrogen content and graphite films. The presence of both of these factors is controlled by the geological history of the lithosphere. Hydrogen in nominally anhydrous minerals behaves as an incompatible element and is preferentially removed during melting or high-temperature tectonothermal events. Grain-boundary graphite films are only stable to ~900 °C so they are also destroyed by high-temperature events. Conversely, tectonic events that enrich the lithosphere in incompatible elements, such as interaction with fluids from a subducting slab or a plume, can introduce both hydrogen and carbon into the lithosphere and therefore increase its electrical conductivity. Case studies of MT results from central Australia and the Slave Craton in Canada suggest that electrical conductivity can act as a proxy for the level of enrichment in incompatible elements of the lithosphere.  相似文献   

3.
Recent studies have shown that major nominally anhydrous minerals in the Earth’s mantle, such as olivine, pyroxene and garnet, can incorporate considerable amounts of water as structurally bound hydroxyl. Even a small amount of water is present in mantle minerals, it can strongly affect a number of physical properties, including density, sound velocity, melting temperature, and electrical conductivities. The presence of water can also influence the dynamic behavior, lead to lateral velocity heterogeneities, and affect the material circulation of the Earth’s deep interior. In particular, seismic studies have reported the existence of low-velocity zones in various locations of the Earth’s upper mantle and transition zone, which has been expected to be associated with the presence of water in the region. In the past two decades, the effect of water on the elasticity and sound velocities of minerals at relevant pressure-temperature (P-T) conditions of the Earth’s mantle attracted extensive interests. Combining the high P-T experimental and theoretical mineralogical results with seismic observations provides crucial constraints on the distribution of water in the Earth’s mantle. In this study, we summarize recent experimental and theoretical mineral physics results on how water affects the elasticity and sound velocity of nominally anhydrous minerals in the Earth’s mantle, which aims to provide new insights into the effect of hydration on the density and velocity profile of the Earth’s mantle, which are of particular importance in understanding of water distribution in the region.  相似文献   

4.
Determining Earth’s structure is a fundamental goal of Earth science, and geophysical methods play a prominent role in investigating Earth’s interior. Geochemical, cosmochemical, and petrological analyses of terrestrial samples and meteoritic material provide equally important insights. Complementary information comes from high-pressure mineral physics and chemistry, i.e., use of sophisticated experimental techniques and numerical methods that are capable of attaining or simulating physical properties at very high pressures and temperatures, thereby allowing recovered samples from Earth’s crust and mantle to be analyzed in the laboratory or simulated computationally at the conditions that prevail in Earth’s mantle and core. This is particularly important given that the vast bulk of Earth’s interior is geochemically unsampled. This paper describes a quantitative approach that combines data and results from mineral physics, petrological analyses of mantle minerals, and geophysical inverse calculations, in order to map geophysical data directly for mantle composition (major element chemistry and water content) and thermal state. We illustrate the methodology by inverting a set of long-period electromagnetic response functions beneath six geomagnetic stations that cover a range of geological settings for major element chemistry, water content, and thermal state of the mantle. The results indicate that interior structure and constitution of the mantle can be well-retrieved given a specific set of measurements describing (1) the conductivity of mantle minerals, (2) the partitioning behavior of water between major upper mantle and transition-zone minerals, and (3) the ability of nominally anhydrous minerals to store water in their crystal structures. Specifically, upper mantle water contents determined here bracket the ranges obtained from analyses of natural samples, whereas transition-zone water concentration is an order-of-magnitude greater than that of the upper mantle and appears to vary laterally underneath the investigated locations.  相似文献   

5.
The transport of water in subduction zones   总被引：9，自引：0，他引：9  
The transport of water from subducting crust into the mantle is mainly dictated by the stability of hydrous minerals in subduction zones. The thermal structure of subduction zones is a key to dehydration of the subducting crust at different depths. Oceanic subduction zones show a large variation in the geotherm, but seismicity and arc volcanism are only prominent in cold subduction zones where geothermal gradients are low. In contrast, continental subduction zones have low geothermal gradients, resulting in metamorphism in cold subduction zones and the absence of arc volcanism during subduction. In very cold subduction zone where the geothermal gradient is very low(?5?C/km), lawsonite may carry water into great depths of ?300 km. In the hot subduction zone where the geothermal gradient is high(25?C/km), the subducting crust dehydrates significantly at shallow depths and may partially melt at depths of 80 km to form felsic melts, into which water is highly dissolved. In this case, only a minor amount of water can be transported into great depths. A number of intermediate modes are present between these two end-member dehydration modes, making subduction-zone dehydration various. Low-T/low-P hydrous minerals are not stable in warm subduction zones with increasing subduction depths and thus break down at forearc depths of ?60–80 km to release large amounts of water. In contrast, the low-T/low-P hydrous minerals are replaced by low-T/high-P hydrous minerals in cold subduction zones with increasing subduction depths, allowing the water to be transported to subarc depths of 80–160 km. In either case, dehydration reactions not only trigger seismicity in the subducting crust but also cause hydration of the mantle wedge. Nevertheless, there are still minor amounts of water to be transported by ultrahigh-pressure hydrous minerals and nominally anhydrous minerals into the deeper mantle. The mantle wedge overlying the subducting slab does not partially melt upon water influx for volcanic arc magmatism, but it is hydrated at first with the lowest temperature at the slab-mantle interface, several hundreds of degree lower than the wet solidus of hydrated peridotites. The hydrated peridotites may undergo partial melting upon heating at a later time. Therefore, the water flux from the subducting crust into the overlying mantle wedge does not trigger the volcanic arc magmatism immediately.  相似文献   

6.
Laboratory Electrical Conductivity Measurement of Mantle Minerals   总被引：4，自引：1，他引：3  
Electrical conductivity structures of the Earth’s mantle estimated from the magnetotelluric and geomagnetic deep sounding methods generally show increase of conductivity from 10−4–10−2 to 100 S/m with increasing depth to the top of the lower mantle. Although conductivity does not vary significantly in the lower mantle, the possible existence of a highly conductive layer has been proposed at the base of the lower mantle from geophysical modeling. The electrical properties of mantle rocks are controlled by thermodynamic parameters such as pressure, temperature and chemistry of the main constituent minerals. Laboratory electrical conductivity measurements of mantle minerals have been conducted under high pressure and high temperature conditions using solid medium high-pressure apparatus. To distinguish several charge transport mechanisms in mantle minerals, it is necessary to measure the electrical conductivity in a wider temperature range. Although the correspondence of data has not been yet established between each laboratory, an outline tendency of electrical conductivity of the mantle minerals is almost the same. Most of mineral phases forming the Earth’s mantle exhibit semiconductive behavior. Dominant conduction mechanism is small polaron conduction (electron hole hopping between ferrous and ferric iron), if these minerals contain iron. The phase transition olivine to high-pressure phases enhances the conductivity due to structural changes. As a result, electrical conductivity increases in order of olivine, wadsleyite and ringwoodite along the adiabat geotherm. The phase transition to post-spinel at the 660 km discontinuity further can enhance the conductivity. In the lower mantle, the conductivity once might decrease in the middle of the lower mantle due to the iron spin transition and then abruptly increase at the condition of the D″ layer. The impurities in the mantle minerals strongly control the formation, number and mobility of charge carriers. Hydrogen in nominally anhydrous minerals such as olivine and high-pressure polymorphs can enhance the conductivity by the proton conduction. However, proton conduction has lower activation enthalpy compared with small polaron conduction, a contribution of proton conduction becomes smaller at high temperatures, corresponding to the mantle condition. Rather high iron content in mantle minerals largely enhances the conductivity of the mantle. This review focuses on a compilation of fairly new advances in experimental laboratory work together with their explanation.  相似文献   

7.
An in-situ microanalysis of Pb isotopic compositions in sulfide minerals is carried out by using femtosecond laser-ablation multi-collector inductively coupled plasma mass spectrometry(fs LA-MC-ICP-MS).High-temperature-activated carbon was used to filter Hg contained in the carrier gas,which reduced the Hg background signal by 48%and also lowered the detection limit of the analysis.Fractionation and mass discrimination effects existing in the ICP-MS analytical processes were corrected using an internal reference Tl in conjunction with an external reference NIST SRM 610.The proposed method was used to analyze the Pb isotopic compositions of chalcopyrite,pyrite,and sphalerite from the Dulong Sn-Zn-In polymetallic ore district.The results showed that in this ore district,the sulfide minerals and different grains of the same sulfide mineral show a large variation in Pb content up to 1000-fold.The studied pyrites show relatively higher Pb contents and homogeneous Pb isotopic compositions,whereas the sphalerites have low Pb contents but most variable Pb isotopic compositions.It is suggested that the large variation of Pb isotopic composition may reflect a late hydrothermal superimposition on the primary sulfide formation.In addition,radiogenic Pb accumulated by radioactive decay of trace amounts of U over time in the host minerals may also be one of the causes for the large variation range of Pb content and Pb isotopic composition of those low-Pb sphalerites.Chalcopyrite and sphalerite grains with Pb content greater than 10 ppm presented a consistent Pb isotopic distribution,whereas all the sulfide grains with Pb content greater than 100 ppm had consistent Pb isotopic composition within 2s measurement uncertainties.The in-situ analysis of Pb isotopic composition agreed well with the results obtained by conventional chemical methods within2s measurement uncertainties,indicating that the data obtained by fs LA-MC-ICP-MS are reliable.Additionally,this study indicates that the Pb isotopic composition could truthfully record the source of ore-forming minerals only for sulfide minerals with high Pb content.On the contrary,the Pb isotopic composition of low-Pb sulfide minerals may be affected by trace amounts of U in the host minerals that may lead to a highly radiogenic Pb isotope ratio.Alternatively,it is also possible that late fluid metasomatic overprinting may alter the Pb isotopic compositions.  相似文献   

8.
Nanofilms of adsorbed water in clay: Mechanism of formation and properties   总被引：1，自引：0，他引：1  
The process of adsorption of water molecules by silicate surfaces of clay minerals is considered. The process leads to the formation of nano-thickness films of adsorbed water. An epitaxial mechanism of nanofilm formation is considered, consisting in the growth of structured hydrate layers under the effect of oxygen and hydroxyl surfaces of clay minerals. The difference between the sizes of hexagonal cells of the solid surface and the forming water film deforms hydrogen bonds and produces inner stress in both the film structure and the mineral lattice. The latter is reflected in the changing size of montmorillonite cell along the b-axis. The thickness of the newly formed adsorption water layer is shown to be controlled by the degree of hydrogen bond deformation, the stress developed inside the nanofilm, the cell size, and the rigidity (strength) of the mineral structure. The deformation of hydrogen bonds and water nanofilm structure determines its specific properties, i.e., wedging pressure, high viscosity, low temperatures of water freezing, dielectric conductivity, etc.  相似文献   

9.
When one end of an air-dry igneous rock block was uniaxially loaded in laboratory, there appeared an electromotive force that made electric currents flow from the stressed volume to the unstressed volume. Quartz-free rocks such as gabbro also generated this force, stronger than quartz-bearing rocks such as granite. This indicates that the piezoelectric effect of quartz and the electrokinetic effect of pore water do not make a large contribution toward generating the electromotive force. We focus on peroxy bond that is one of the abundant lattice defects in igneous rock-forming minerals. When mechanical loading deforms the lattice structure around this defect and breaks its bond, its energy levels change and act like an accepter. As an electron is trapped at this defect from a neighbor O2- site, a positive hole is activated there. They attempt to diffuse toward the unstressed volume through the valence band and are simultaneously affected by the attractive electric force with the electrons trapped in peroxy bonds. This leads to a polarization in the stressed volume and the generation of electromotive force between the stressed and unstressed volumes. Similar electromotive force may be generated in the Earth's crust where inhomogeneous stress/strain is changing.  相似文献   

10.
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11.
Hu  Xiangyun  Lin  Wule  Yang  Wencai  Yang  Bo 《中国科学:地球科学(英文版)》2020,63(11):1661-1677

Cratons have a long history of evolution. In this paper, applications of the magnetotelluric method used in the study of craton lithosphere over the past 30 years were reviewed, examining case studies of cratons in North America, South America, Asia, Australia, and Africa. The nuclei of the Archean cratons, for example the Kalahari Craton and Rae Craton, are usually characterized by thick and highly resistive lithospheric roots. During or after the formation of the cratons, tectonothermal events, such as collision, mantle plume, and asthenosphere upwelling led to the formation of high-conductivity zones in the craton lithosphere, which could be attributed to the increased hydrogen content (of nominally anhydrous minerals), higher iron content, and formation of graphite films or sulfides along the grain boundary of minerals. These conductive zones are characterized by resistivity discontinuities in craton lithosphere. In particular, the conductive zones include (1) large-scale lithospheric mantle conductors beneath the Slave Craton, Gawler Craton, and central part of North China Craton(Trans-North China Orogen); (2) near-vertical high-conductivity zone associated with the fossil subduction zone beneath the Dharwar Craton and Slave Craton; and (3) regional lateral electrical discontinuities, such as a conductive anomaly under the Bushveld Complex of the Kaapvaal Craton. The eMoho refers to the electrical discontinuity in the crust-mantle boundary. In existing research, this has been detected under the condition of extremely high lithospheric resistivity with only a slight decrease in the lower crust, and in the case of a very thin conductive lower crust or the lack thereof. In the resistivity model, the unique “mushroom-like” lower crust-lithosphere mantle conductor and very thin lower crust layer of the North China Craton may represent lithosphere destruction and/or thinning. We also find that some of the cratons are still not well understood. Therefore, extensive three-dimensional inversion and joint interpretation of geochemical, geophysical, and geologic data are necessary to understand the tectonic evolutionary history of craton lithosphere.

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12.
This paper considers the chemical composition and classification of ground water at seven flowing wells and four springs using materials from the 2014 hydrogeochemical sampling and from continuous observations conducted by the Kamchatka Branch of the Geophysical Survey of the Russian Academy of Sciences (KB GS RAS) in 1989–1999. We estimated the saturation of ground water discharges at individual vents with alumosilicate, carbonate, and sulfate secondary minerals, following the behavior of saturation over time. We have found that the ground water undergoes an increase in the saturation with secondary minerals during large earthquakes that produced shaking of intensity I = 5–6 on the MSK-64 scale. Such changes in the saturation of ground water with secondary minerals are less pronounced during the precursory periods before earthquake occurrence. We discuss desirable future developments of the observational system at wells and springs in order to look for new types of hydrogeochemical precursors to earthquakes.  相似文献   

13.
By the theories of potential flow and structural vibration, the formulae for evaluating the ‘wet’ (with water) frequencies and mode shapes of the beam‐supported aqueduct are derived through a simplified fluid‐structure interaction analysis. The time‐history formulae of structural responses to the vertical seismic excitation are obtained. Applying the response‐spectrum principle, the equivalent vertical earthquake load exerted on the beam and the corresponding effects are also derived. Several illustrative examples are conducted. The analytical results show that: (i) The ‘wet’ frequencies of the structure are lower than the corresponding ‘dry’ (without water) frequencies due to the participating water mass, but the ‘wet’ mode shapes are identical to the corresponding ‘dry’ ones. (ii) The water mass plays an important role in the vertical seismic response, which varies with the different geological sites. For the different seismic inputs, the deeper the water is, the greater are the structural responses. (iii) The vertical seismic effects on the beam are generally not too small to be neglected and should be considered in the structural designs of a beam‐supported aqueduct. Copyright © 2002 John Wiley & Sons, Ltd.  相似文献   

14.
Mineralogical and hydrogen isotopic studies have been made on clay minerals occurring in the Ohnuma geothermal area, northeastern Japan. Here, clay minerals such as smectite, kaolinite, dickite, sericite, and chlorite were formed by hydrothermal alteration of Miocene rocks. A chemical equilibrium can be assumed to be attained from the fact that the amount of expandable layer in the interstratified chlorite/smectite decreases and the polytype of sericite changes from 1M to 2M1 with increasing depth and temperature. The hydrogen isotopic composition (D/H) of the clay minerals is lighter than that of the geothermal and local meteoric waters by about 20–40‰. The hydrogen isotopic fractionation factors αmineral-water are as follows: 0.972–0.985 for kaolinite and dickite, 0.973–0.977 for sericite, and 0.954–0.987 for chlorite. In the temperature range from 100 to 250°C, the hydrogen isotopic fractionation factors between these minerals and water are not sensitive to the temperature. αchlorite-water depends on the kind of octahedrally coordinated cations which lie close to the hydroxyl groups; it becomes large with an increase of Mg content of chlorite.  相似文献   

15.
Electromagnetic measurements have demonstrated that the lower continental crust has remarkable electrical anomalies of high conductivity and electrical anisotropy on a global scale (probably with some local exceptions), but their origin is a long-standing and controversial problem. Typical electrical properties of the lower continental crust include: (1) the electrical conductivity is usually 10−4 to 10−1 S/m; (2) the overlying shallow crust and underlying upper mantle are in most cases less conductive; (3) the electrical conductivity is statistically much higher in Phanerozoic than in Precambrian areas; (4) horizontal anisotropy has been resolved in many areas; and (5) in some regions there appear to be correlations between high electrical conductivity and other physical properties such as seismic reflections. The explanation based on conduction by interconnected, highly conductive phases such as fluids, melts, or graphite films in grain boundary zones has various problems in accounting for geophysically resolved electrical conductivity and other chemical and physical properties of the lower crust. The lower continental crust is dominated by mafic granulites (in particular beneath stable regions), with nominally anhydrous clinopyroxene, orthopyroxene, and plagioclase as the main assemblages, and the prevailing temperatures are mostly 700–1,000°C as estimated from xenolith data, surface heat flow, and seismic imaging. Pyroxenes have significantly higher Fe content in the lower crust than in the upper mantle (peridotites), and plagioclase has higher Na content in the lower crust than in the shallow crust (granites). Minerals in the lower continental crust generally contain trace amounts of water as H-related point defects, from less than 100 to more than 1,000 ppm H2O (by weight), with concentrations usually higher than those in the upper mantle. Observations of xenolith granulites captured by volcano-related eruptions indicate that the lower continental crust is characterized by alternating pyroxene-rich and plagioclase-rich layers. Experimental studies on typical lower crustal minerals have shown that their electrical conductivity can be significantly enhanced by the higher contents of Fe (for pyroxenes), Na (for plagioclase), and water (for all minerals) at thermodynamic conditions corresponding to the lower continental crust, e.g., to levels comparable to those measured by geophysical field surveys. Preferred orientation of hydrous plagioclase, e.g., due to ductile flow in the deep crust, and alternating mineral fabrics of pyroxene-rich and plagioclase-rich layers can lead to substantial anisotropy of electrical conductivity. Electrical conductivity properties in many regions of the lower continental crust, especially beneath stable areas, can mostly be accounted for by solid-state conduction due to the major constituents; other special, additional conduction mechanisms due to grain boundary phases are not strictly necessary.  相似文献   

16.
Obtaining a continuous sedimentary record of Cenozoic East Asian paleoclimate change is key to understand the origin, evolution and driving mechanism of the East Asian monsoon and climate change. Based on the continuous Cenozoic fluvial and lacustrine sedimentary sequence in the Weihe Basin, central China, we carried out research on the content and crystal parameters of clay minerals. The paleoclimate change since the middle Eocene was reconstructed accordingly. The results show that smectite and illite are the dominant clay minerals in fluvial-lacustrine sediments of Weihe Basin. The crystallinity of illite,the chemical index of illite, the ratio of smectite to illite and chlorite decrease gradually, which indicates that chemical weathering in the Weihe River watershed stepwise weakened since the middle Eocene, under the background of a semi-arid and semi-humid climate. The formation of palygorskite may be affected by a weak diagenesis. In this case, the content of smectite and the illite crystallinity caused by the weathering in the corresponding period may be actually higher than that of the current,which indicates that the climate in the Weihe Basin region was relatively warm and humid from the middle Eocene to Pliocene.With the decrease of Cenozoic global temperature and the continuous accumulation of sediments, the intensity of chemical weathering in the Weihe Basin gradually weakened, and the East Asian monsoon climate gradually evolved until becoming dry in the Quaternary. Evidence from clay minerals also indicates that the aridification in the Weihe Basin from the late Eocene to the Oligocene may be a response to the global cooling event at the Eocene-Oligocene transition.  相似文献   

17.
Using Fourier transform infrared spectroscopy (FTIR), we measured water contents of quartz and feldspar for four thin sections of felsic mylonite and two thin sections of banded granitic gneiss col- lected from a ductile shear zone of middle crust along the Red Rivers-Ailaoshan active fault. The ab- sorbance spectra and peak position suggest that water in quartz and feldspar of granitic gneiss and felsic mylonite occurs mainly as hydroxyl in crystal defect, but also contains inclusion water and grain boundary water. The water contents of minerals were calculated based on the absorbance spectra. Water content of feldspar in granitic gneiss is 0.05 wt%-0.15 wt%, and that of quartz 0.03 wt%-0.09 wt%. Water content of feldspar ribbon and quartz ribbon in felsic mylonite is 0.095 wt%-0.32 wt%, and those of fine-grained feldspar and quartz are 0.004 wt%-0.052 wt%. These data show that the water content of weakly deformed feldspar and quartz ribbons is much higher than that of strongly deformed fine-grained feldspar and quartz. This suggests that strong shear deformation leads to breakage of the structures of constitutional water, inclusion and grain boundary water in feldspar and quartz, and most of water in minerals of mylonite is released to the upper layer in the crust.  相似文献   

18.
Mineral weathering rates and a forest macronutrient uptake stoichiometry were determined for the forested, metabasaltic Hauver Branch watershed in north‐central Maryland, USA. Previous studies of Hauver Branch have had an insufficient number of analytes to permit determination of rates of all the minerals involved in chemical weathering, including biomass. More equations in the mass‐balance matrix were added using existing mineralogic information. The stoichiometry of a deciduous biomass term was determined using multi‐year weekly to biweekly stream‐water chemistry for a nearby watershed, which drains relatively unreactive quartzite bedrock. At Hauver Branch, calcite hosts ~38 mol% of the calcium ion (Ca2+) contained in weathering minerals, but its weathering provides ~90% of the stream water Ca2+. This occurs in a landscape with a regolith residence time of more than several Ka (kiloannum). Previous studies indicate that such old regolith does not typically contain dissolving calcite that affects stream Ca2+/Na+ ratios. The relatively high calcite dissolution rate likely reflects dissolution of calcite in fractures of the deep critical zone. Of the carbon dioxide (CO2) consumed by mineral weathering, calcite is responsible for approximately 27%, with the silicate weathering consumption rate far exceeding that of the global average. The chemical weathering of mafic terrains in decaying orogens thus may be capable of influencing global geochemical cycles, and therefore, climate, on geological timescales. Based on carbon‐balance calculations, atmospheric‐derived sulfuric acid is responsible for approximately 22% of the mineral weathering occurring in the watershed. Our results suggest that rising air temperatures, driven by global warming and resulting in higher precipitation, will cause the rate of chemical weathering in the Hauver Branch watershed to increase until a threshold temperature is reached. Beyond the threshold temperature, increased recharge would produce a shallower groundwater table and reduced chemical weathering rates. Copyright © 2013 John Wiley & Sons, Ltd.  相似文献   

19.
The possible effect of pressure-induced breakdown of amphibole in triggering explosive eruptions is considered. Since amphibole is a hydrous mineral, when it breaks down to an anhydrous assemblage as pressure is reduced to less than 1.5–2 kbar, the water liberated might oversaturate the coexisting melt generating the necessary overpressure to trigger an explosive eruption. Resorbed amphiboles are commonly observed in evolved lavas and pyroclastic ejecta. The amount of a volatile component, such as water that will dissolve in a melt is a function of pressure, temperature and composition, and during crystallization it is also a function of the extent of crystallization and the nature of crystallizing minerals. The relation can be expressed by the simple equation: where Xr is the water content of the residual liquid, Xi is the initial water content, XmOH, is the water content of hydrous minerals, f is the total extent of crystallization and f′ is the extent of crystallization of hydrous minerals such that 0 ≤ f′ ≤ f ≤ 1. We suggest that storage of water in hydrous minerals, such as amphibole and biotite, plays an important role in the eruptive behavior of certain types of magmas; the breakdown of these minerals liberates water to the melt at a rate governed by the kinetics of the resorption reaction. If the release of water causes the liquid fraction to exceed the solubility limit and the overpressure resulting from expansion of the gas exceeds the strength of the overlying magma and rocks in the conduit, the result can be an explosive eruption. The amphibole effect can occur at different structural levels depending on the nature of the magma and physical conditions leading to instability.  相似文献   

20.
Gaseous components of gas inclusions in deep carbonate rocks (>5700 m) from the Tacan 1 well were analyzed by online mass spectrometry by means of either the stepwise heating technique or vacuum electromagnetism crushing. The carbon isotopic compositions of gases released by vacuum electromagnetism crushing were also measured. Although the molecular compositions of gas inclusions show differences between the two methods, the overall characteristics are that gas inclusions mainly contain CO2, whilst hydrocarbon gases, such as CH4, C2H6 and C3H8, are less abundant. The content of CO is higher in the stepwise heating experiment than that in the method of vacuum electromagnetism crushing, and there are only minor amounts of N2, H2 and O2 in gas inclusions. Methane δ13C values of gas inclusions in Lower Ordovician and Upper Cambrian rocks (from 5713.7 to 6422 m; -52‰-63‰) are similar to those of bacterial methane, but their chemical compositions do not exhibit the dry character in comparison with biogenic gases. These characteristics of deep gas inclusions may be related to the migration fractionation. Some deep natural gases with light carbon isotopic characteristics in the Tazhong Uplift may have a similar origin. The δ13C1 values of gas inclusions in Lower Cambrian rocks (7117-7124 m) are heavier (-39‰), consistent with highly mature natural gases. Carbon isotopic compositions of CO2 in the gas inclusions of deep carbonate rocks are similar (from -4‰ to -13‰) to those of deep natural gases, indicating predominantly an inorganic origin.  相似文献   

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