Influence of seismic vibrations on the development of tectonic deformations     

V.?V.?Adushkin  G.?G.?KocharyanEmail author  D.?V.?Pavlov  E.?A.?Vinogradov  A.?I.?Goncharov  V.?I.?Kulikov  A.?A.?Kulyukin 《Doklady Earth Sciences》2009,426(1):588-590

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Determining mineral weathering rates based on solid and solute weathering gradients and velocities: application to biotite weathering in saprolites     

Art F. White   《Chemical Geology》2002,190(1-4):69-89

Chemical weathering gradients are defined by the changes in the measured elemental concentrations in solids and pore waters with depth in soils and regoliths. An increase in the mineral weathering rate increases the change in these concentrations with depth while increases in the weathering velocity decrease the change. The solid-state weathering velocity is the rate at which the weathering front propagates through the regolith and the solute weathering velocity is equivalent to the rate of pore water infiltration. These relationships provide a unifying approach to calculating both solid and solute weathering rates from the respective ratios of the weathering velocities and gradients. Contemporary weathering rates based on solute residence times can be directly compared to long-term past weathering based on changes in regolith composition. Both rates incorporate identical parameters describing mineral abundance, stoichiometry, and surface area.

Weathering gradients were used to calculate biotite weathering rates in saprolitic regoliths in the Piedmont of Northern Georgia, USA and in Luquillo Mountains of Puerto Rico. Solid-state weathering gradients for Mg and K at Panola produced reaction rates of 3 to 6×10⁻¹⁷ mol m⁻² s⁻¹ for biotite. Faster weathering rates of 1.8 to 3.6×10⁻¹⁶ mol m⁻² s⁻¹ are calculated based on Mg and K pore water gradients in the Rio Icacos regolith. The relative rates are in agreement with a warmer and wetter tropical climate in Puerto Rico. Both natural rates are three to six orders of magnitude slower than reported experimental rates of biotite weathering.  相似文献   

Les minéraux techniques naturels : connaissance,typologie et propriétés d'usageNatural technical minerals: investigation,typology and utilisation properties     

Jacques Yvon  Jean-Maurice Cases  Frédéric Villiéras  Laurent Michot  Fabien Thomas 《Comptes Rendus Geoscience》2002,334(9):717-730

By nature minerals are heterogeneous materials for many of their properties. These properties also vary according to composition and structure fluctuations, compared to definitions. Technical minerals are used in applications where their performances depend on intrinsic properties and processing conditions. It is possible to base rankings on simple criteria, allowing estimating the abilities of minerals for each utilisation. The research of the corresponding mechanisms concerns the molecular level. These questions are discussed for kaolins, raw materials for baked clays, talqueous materials and montmorillonites. To cite this article: J. Yvon et al., C. R. Geoscience 334 (2002) 717–730.  相似文献   

The ubiquitous nature of accessory calcite in granitoid rocks: Implications for weathering, solute evolution, and petrogenesis   总被引：3，自引：0，他引：3  

Art F. White  Jacob B. Lowenstern  Davison V. Vivit  Thomas D. Bullen 《Geochimica et cosmochimica acta》2005,69(6):1455-1471

Calcite is frequently cited as a source of excess Ca, Sr and alkalinity in solutes discharging from silicate terrains yet, no previous effort has been made to assess systematically the overall abundance, composition and petrogenesis of accessory calcite in granitoid rocks. This study addresses this issue by analyzing a worldwide distribution of more than 100 granitoid rocks. Calcite is found to be universally present in a concentration range between 0.028 to 18.8 g kg⁻¹ (mean = 2.52 g kg⁻¹). Calcite occurrences include small to large isolated anhedral grains, fracture and cavity infillings, and sericitized cores of plagioclase. No correlation exists between the amount of calcite present and major rock oxide compositions, including CaO. Ion microprobe analyses of in situ calcite grains indicate relatively low Sr (120 to 660 ppm), negligible Rb and ⁸⁷Sr/⁸⁶Sr ratios equal to or higher than those of coexisting plagioclase. Solutes, including Ca and alkalinity produced by batch leaching of the granitoid rocks (5% CO₂ in DI water for 75 d at 25°C), are dominated by the dissolution of calcite relative to silicate minerals. The correlation of these parameters with higher calcite concentrations decreases as leachates approach thermodynamic saturation. In longer term column experiments (1.5 yr), reactive calcite becomes exhausted, solute Ca and Sr become controlled by feldspar dissolution and ⁸⁷Sr/⁸⁶Sr by biotite oxidation. Some accessory calcite in granitoid rocks is related to intrusion into carbonate wall rock or produced by later hydrothermal alteration. However, the ubiquitous occurrence of calcite also suggests formation during late stage (subsolidus) magmatic processes. This conclusion is supported by petrographic observations and ⁸⁷Sr/⁸⁶Sr analyses. A review of thermodynamic data indicates that at moderate pressures and reasonable CO₂ fugacities, calcite is a stable phase at temperatures of 400 to 700°C.  相似文献   

Carbon in silicate liquids: the systems NaAlSi3O8-CO2, CaAl2Si2O8-CO2, and KAlSi3O8-CO2     

Art Boettcher  Robert W. Luth  Bradford S. White 《Contributions to Mineralogy and Petrology》1987,97(3):297-304

To further our knowledge of the effects of volatile components on phase relationships in aluminosilicate systems, we determined the vapor saturated solidi of albite, anorthite, and sanidine in the presence of CO₂ vapor. The depression of the temperature of the solidus of albite by CO₂ decreases from 30° C at 10 kbar, to 10° C at 20 kbar, to about 0 at 25 kbar, suggesting that the solubility of CO₂ in NaAlSi₃O₈ liquid in equilibrium with solid albite decreases with increasing pressure and temperature. In contrast, CO₂ lowers the temperature of the solidus of anorthite by 30° C at 14 kbar, and by 70dg C at 25 kbar. This contrasting behavior of albite and anorthite is also reflected in the behavior of melting in the absence of volatile components. Whereas albite melts congruently to a liquid of NaAl-Si₃O₈ composition to pressures of 35 kbar, anorthite melts congruently to only about 10 kbar and, at higher pressures, incongruently to corundum plus a liquid that is enriched in SiO₂ and CaO and depleted in Al₂O₃ relative to CaAl₂Si₂O₈.The tendency toward incongruent melting with increasing pressure in albite and anorthite produces an increase in the activity of SiO₂ component in the liquid ( ). We predict that this increases the ratio of molecular CO₂/CO ₃ ^2– in these liquids, but the experimental results from other workers are mutually contradictory. Because of the positive dP/dT of the albite solidus and the negative dP/dT of the anorthite solidus, we propose that a negative temperature derivative of the solubility of molecular CO₂ in plagioclase liquids may partly explain the decrease in solubility of carbon with increasing pressure in near-solidus NaAlSi₃O₈ liquids, which is in contrast to that in CaAl₂Si₂O₈ liquid. Also, reaction of CO₂ with NaAlSi₃O₈ liquid to form CO ₃ ^2– that is complexed with Na⁺ must be accompanied by a change in Al³⁺ from network-former to network-modifier, as Na⁺ is no longer abailable to charge-balance Al³⁺ in a network-forming role. However, when anorthite melts incongruently to corundum plus a CaO-rich liquid, the complexing of CO ₃ ^2– with the excess Ca²⁺ in the liquid does not require a change in the structural role of aluminum, and it may be more energetically favorable.The depression of the temperature of the solidus of sanidine resulting from the addition of CO₂ increases from 50° C at 5 kbar to 170° C at 15 kbar. In marked contrast to the plagioclase feldspars, sanidine melts incongruently to leucite plus a SiO₂-rich liquid up to the singular point at 15 kbar. Above this pressure, sanidine melts congruently, resulting in a decrease in the with increasing pressure in the interval up to 15 kbar. Above this pressure, the congruent melting of sanidine results in a lower and nearly constant relative to those of albite and anorthite, and CO₂ produces a nearly constant freezing-point depression of about 170° C. Because of the low at pressures above the singular point, we infer that most of the carbon dissolves as CO ₃ ^2– , resulting in a low CO₂/ CO ₃ ^2– , but a high total carbon content.The principles derived from the studies of phase equilibria in these chemically simple systems provide some information on the structural and thermal properties of magmas. We propose that the is an important parameter in controlling the speciation of carbon in these feldspathic liquids, but it certainly is not the only factor, and it may be relatively less significant in more complex compositions. In addition, our phase-equilibria approach does not provide direct thermal and structural information as do calorimetry and spectroscopy, but the latter have been used primarily on glasses (quenched liquids) and cannot be used in situ to derive direct information on liquids at elevated pressures, as can our method. Hopefully, the results of all of these approaches can be integrated to yield useful results.Institute of Geophysics and Planetary Physics, Contribution No. 2744  相似文献   

On the sensitivity characteristics of Lacoste & Romberg gravimeter (model G)     

Ichiro Nakagawa  Sinzi Nakai  Ryūichi Shichi  Hirokazu Tajima  Sadakatu Izutuya  Yoshiteru Kono  Toshihiro Higashi  Hiromi Fujimoto  Makoto Murakami  Kazuo Tajima  Minoru Funaki 《Journal of Geodesy》1985,59(1):55-67

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Surface chemistry and dissolution kinetics of glassy rocks at 25°C     

Art F White 《Geochimica et cosmochimica acta》1983,47(4):805-815

The weathering rates and mechanisms of three types of glassy rocks were investigated experimentally at 25 °C, pH 1.0 to 6.2, and reaction times as much as to 3 months. Changes in major element chemistry were monitored concurrently as a function of time in the aqueous solution and within the near surface region of the glass. Leach profiles, obtained by a HF leaching technique, displayed near-surface zones depleted in major cations. These zones increased in depth with increasing time and decreasing pH of reactions. Release rates into the aqueous solution were parabolic for Na and K and linear for Si and Al. A coupled weathering model, involving surface dissolution with concurrent diffusion of Na, K, and Al, produced a mass balance between the aqueous and glass phases. Steady state conditions are reached at pH 1.0 after approximately 3 weeks of reaction. Steady-state is not reached even after 3 months at pH 6.2.An interdiffusion model describes observed changes in Na diffusion profiles for perlite at pH 1.0. The calculated Na self-diffusion coefficient of 5 × 10^?19 cm²·s^?1 at 25°C approximates coefficients extrapolated from previously reported high temperature data for obsidian. The self-diffusion coefficient for H₃O⁺, 1.2 × 10^?20 cm²·s^?1, is similar to measured rates of water diffusion during hydration of obsidian to form perlite.  相似文献   

Development and evolution of water vapor vesicles during fast thermal breakdown of muscovite     

K. Devineau  F. Villiéras  O. Barrès 《Physics and Chemistry of Minerals》2007,34(8):559-572

At 1,175°C-1 bar, muscovite in natural granite powders is completely transformed after 5 min. Due to the overlapping of several processes such as dehydroxylation, mineralogical transformations, collapse and sintering of transformed lamellae, a few parts per thousand of H₂O vapor are trapped, generating bubbles in muscovite pseudomorphs. For short durations (5–40 min), the crystallographic properties of the precursor muscovite control the geometry of the bubbles that may be compared to thick disks with a rounded shape in basal sections and an elongated shape in lateral section, parallel to the former cleavage planes of muscovite. With longer durations the bubbles change from thick disks to spheres, which can be explained by the release of constraints perpendicular to basal planes upon growth of the high temperature Si–Al oxides. With time, the number of bubbles decreases while the bubble size and the porosity of the pseudomorphs increase. Bubble behavior was analyzed in terms of ripening, shape transformations and coalescence.  相似文献