A possible effect of melt structure on the Mg-Fe partitioning between olivine and melt     

Ikuo Kushiro  Bjorn O Mysen 《Geochimica et cosmochimica acta》2002,66(12):2267-2272

Partitioning of Mg and Fe²⁺ between olivine and mafic melts has been determined experimentally for eight different synthetic compositions in the temperature range between 1335 and 1425°C at 0.1 MPa pressure and at fo₂ ∼1 log unit below the quartz-fayalite-magnetite buffer. The partition coefficient [K_D = (Fe²⁺/Mg)^ol/(Fe²⁺/Mg)^melt] increases from 0.25 to 0.34 with increasing depolymerization of melt (NBO/T of melt from 0.25-1.2), and then decreases with further depolymerization of melt (NBO/T from 1.2-2.8). These variations are similar to those observed in natural basalt-peridotite systems. In particular, the variation in NBO/T ranges for basaltic-picritic melts (0.4-1.5) is nearly identical to that obtained in the present experiments. Because the present experiments were carried out at constant pressure (0.1 MPa) and in a relatively small temperature range (90°C), the observed variations of Mg and Fe²⁺ partitioning between olivine and melt must depend primarily on the composition or structure of melt. Such variations of K_D may depend on the relative proportions of four-, five-, and six-coordinated Mg²⁺ and Fe²⁺ in melt as a function of degree of NBO/T.  相似文献   

Seasonal air temperature variations retrieved from a Geladaindong ice core, Tibetan Plateau     

ZHANG Yongjun  KANG Shichang  QIN Dahe  REN Jiawen  ZHANG Yulan  Bjorn GRIGHOLM  Paul MAYEWSKI 《地理学报》2007,17(4):431-441

A 70-year history of precipitation δ18O record has been retrieved using an ice core drilled from a plat portion of the firn area in the Guoqu Glacier (33o34′37.8″ N, 91o10′35.3″ E, 5720 m a.s.l.) on Mt. Geladaindong (the source region of Yangtze River) during October and November, 2005. Based on the seasonality of δ18O records and the significant positive rela-tionships between monsoon/non-monsoon δ18O values and summer/spring air temperature from the nearby meteorological stations, the history of summer and spring air temperature have been reconstructed for the last 70 years. The results show that both summer and spring air temperature variations present similar trends during the last 70 years. Regression analysis indicates that the slope of the temperature-δ18O relationship is 1.3℃/‰ for non-monsoon δ18O values and spring air temperature, and 0.4℃/‰ for monsoon δ18O values and summer air temperature. Variation of air temperature recorded in the ice core is consistent with that in the Northern Hemisphere (NH), however, the warming trend in the Geladaindong region is more intense than that in the NH, reflecting a higher sensitivity to global warming in the high elevation regions. In addition, warming trend is greater in spring than in summer.  相似文献   

Equivalent time-average and effective medium for periodic layers     

Alexey Stovas  Bjorn Ursin 《Geophysical Prospecting》2007,55(6):871-882

The propagation of acoustic waves through a periodic layered medium is analyzed by an eigenvalue decomposition of the propagator matrix. This reveals how the velocity and attenuation of the layered medium vary as function of the periodic structure, material parameters and frequency. There are two important parameters which control the wave propagation in the periodic medium: the reflection coefficient and the ratio between one‐way traveltimes of the two parts of the cyclic layered medium. For low frequencies (large values of wavelength to layer thickness), the layered structure behaves as an effective medium, then there is a transition zone, and for higher frequencies (small values of wavelength to layer thickness) the medium is described by the time‐average velocity. In this paper we mostly concentrate on the transition zone between an effective medium and time‐average medium regimes. The width of the transition zone increases with larger values of the reflection coefficient. The transition zone corresponds to a blocking regime for which the transmission response of the layered structure is close to zero. For even higher frequencies, the time‐average medium is replaced by a new transition zone, and then again a time‐average medium. This pattern is periodically repeated with higher frequencies. For small values of the reflection coefficient, the transition between effective medium and time‐average medium occurs around a value of wavelength to layer thickness equal to 4.  相似文献   

Solubility and solution mechanisms of C-O-H volatiles in silicate melt with variable redox conditions and melt composition at upper mantle temperatures and pressures     

Bjorn O. Mysen  Kathryn Kumamoto  Marilyn L. Fogel 《Geochimica et cosmochimica acta》2011,75(20):6183-6199

Solubility and solution mechanisms in silicate melts of oxidized and reduced C-bearing species in the C-O-H system have been determined experimentally at 1.5 GPa and 1400 °C with mass spectrometric, NMR, and Raman spectroscopic methods. The hydrogen fugacity, f_H2, was controlled in the range between that of the iron-wüstite-H₂O (IW) and the magnetite-hematite-H₂O (MH) buffers. The melt polymerization varied between those typical of tholeiitic and andesitic melts.The solubility of oxidized (on the order of 1-2 wt% as C) and reduced carbon (on the order of 0.15-0.35 wt% as C) is positively correlated with the NBO/Si (nonbridging oxygen per silicon) of the melt. At given NBO/Si-value, the solubility of oxidized carbon is 2-4 times greater than under reducing conditions. Oxidized carbon dioxide is dissolved as complexes, whereas the dominant reduced species in melts are CH₃-groups forming bonds with Si⁴⁺ together with molecular CH₄. Formation of complexes results in silicate melt polymerization (decreasing NBO/Si), whereas solution of reduced carbon results in depolymerization of melts (increasing NBO/Si).Redox melting in the Earth’s interior has been explained with the aid of the different solution mechanisms of oxidized and reduced carbon in silicate melts. Further, effects of oxidized and reduced carbon on melt viscosity and on element partitioning between melts and minerals have been evaluated from relationships between melt polymerization and dissolved carbon combined with existing experimental data that link melt properties and melt polymerization. With total carbon contents in the melts on the order of several mol%, mineral/melt element partition coefficients and melt viscosity can change by several tens to several hundred percent with variable redox conditions in the range of the Earth’s deep crust and upper mantle.  相似文献   

The solution behavior of H₂O in peralkaline aluminosilicate melts at high pressure with implications for properties of hydrous melts     

Bjorn O. Mysen 《Geochimica et cosmochimica acta》2007,71(7):1820-1834

Solubility and solution mechanisms of H₂O in depolymerized melts in the system Na₂O-Al₂O₃-SiO₂ were deduced from spectroscopic data of glasses quenched from melts at 1100 °C at 0.8-2.0 GPa. Data were obtained along a join with fixed nominal NBO/T = 0.5 of the anhydrous materials [Na₂Si₄O₉-Na₂(NaAl)₄O₉] with Al/(Al+Si) = 0.00-0.25. The H₂O solubility was fitted to the expression, X_H2O=0.20+0.0020f_H2O-0.7X_Al+0.9(X_Al)², where X_H2O is the mole fraction of H₂O (calculated with O = 1), f_H2O the fugacity of H₂O, and X_Al = Al/(Al+Si). Partial molar volume of H₂O in the melts, , calculated from the H₂O-solulbility data assuming ideal mixing of melt-H₂O solutions, is 12.5 cm³/mol for Al-free melts and decreases linearly to 8.9 cm³/mol for melts with Al/(Al+Si) ∼ 0.25. However, if recent suggestion that is composition-independent is applied to constrain activity-composition relations of the hydrous melts, the activity coefficient of H₂O, , increases with Al/(Al+Si).Solution mechanisms of H₂O were obtained by combining Raman and ²⁹Si NMR spectroscopic data. Degree of melt depolymerization, NBO/T, increases with H₂O content. The rate of NBO/T-change with H₂O is negatively correlated with H₂O and positively correlated with Al/(Al+Si). The main depolymerization reaction involves breakage of oxygen bridges in Q⁴-species to form Q² species. Steric hindrance appears to restrict bonding of H⁺ with nonbridging oxygen in Q³ species. The presence of Al³⁺ does not affect the water solution mechanisms significantly.  相似文献   

Solution behavior of reduced COH volatiles in silicate melts at high pressure and temperature     

Bjorn O. Mysen  Marilyn L. Fogel  George D. Cody 《Geochimica et cosmochimica acta》2009,73(6):1696-6003

The solubility and solution mechanisms of reduced COH volatiles in Na₂OSiO₂ melts in equilibrium with a (H₂ + CH₄) fluid at the hydrogen fugacity defined by the iron-wüstite + H₂O buffer [f_H2(IW)] have been determined as a function of pressure (1-2.5 GPa) and silicate melt polymerization (NBO/Si: nonbridging oxygen per silicon) at 1400 °C. The solubility, calculated as CH₄, increases from ∼0.2 wt% to ∼0.5 wt% in the melt NBO/Si-range ∼0.4 to ∼1.0. The solubility is not significantly pressure-dependent, probably because f_H2(IW) in the 1-2.5 GPa range does not vary greatly with pressure. Carbon isotope fractionation between methane-saturated melts and (H₂ + CH₄) fluid varied by ∼14‰ in the NBO/Si-range of these melts.The (C..H) and (O..H) speciation in the quenched melts was determined with Raman and ¹H MAS NMR spectroscopy. The dominant (C..H)-bearing complexes are molecular methane, CH₄, and a complex or functional group that includes entities with CCH bonding. Minor abundance of complexes that include SiOCH₃ bonding is tentatively identified in some melts. There is no spectroscopic evidence for SiC or SiCH₃. Raman spectra indicate silicate melt depolymerization (increasing NBO/Si). The [CH₄/CCH]^melt abundance ratio is positively correlated with NBO/Si, which is interpreted to suggest that the (CCH)-containing structural entity is bonded to the silicate melt network structure via its nonbridging oxygen. The ∼14‰ carbon isotope fractionation change between fluid and melt is because of the speciation changes of carbon in the melt.  相似文献   

Structure and Dynamical Influence of Water Vapor in the Lower Tropical Troposphere     

Bjorn Stevens  Hélène Brogniez  Christoph Kiemle  Jean-Lionel Lacour  Cyril Crevoisier  Johannes Kiliani 《Surveys in Geophysics》2017,38(6):1371-1397

In situ, airborne and satellite measurements are used to characterize the structure of water vapor in the lower tropical troposphere—below the height, \(z_*,\) of the triple-point isotherm, \(T_*.\) The measurements are evaluated in light of understanding of how lower-tropospheric water vapor influences clouds, convection and circulation, through both radiative and thermodynamic effects. Lower-tropospheric water vapor, which concentrates in the first few kilometers above the boundary layer, controls the radiative cooling profile of the boundary layer and lower troposphere. Elevated moist layers originating from a preferred level of convective detrainment induce a profile of radiative cooling that drives circulations which reinforce such features. A theory for this preferred level of cumulus termination is advanced, whereby the difference between \(T_*\) and the temperature at which primary ice forms gives a ‘first-mover advantage’ to glaciating cumulus convection, thereby concentrating the regions of the deepest convection and leading to more clouds and moisture near the triple point. A preferred level of convective detrainment near \(T_*\) implies relative humidity reversals below \(z*\) which are difficult to identify using retrievals from satellite-borne microwave and infrared sounders. Isotopologues retrievals provide a hint of such features and their ability to constrain the structure of the vertical humidity profile merits further study. Nonetheless, it will likely remain challenging to resolve dynamically important aspects of the vertical structure of water vapor from space using only passive sensors.  相似文献   

太阳的背面     

Bjorn Carey  胡德良 《海洋地质前沿》2006,22(11):40-40

在太阳上,看不到的那一面足以把你烤焦。太阳自转很慢,大约一个月才能转一周,这就意味着太阳另一面的每次活动会隐藏长达两周的时间。如果另一面正在形成一场巨大的磁暴,当太阳最终转到朝向地球时,磁暴就会携带大量的辐射袭击地球。这种情况在2003年发生过。当时意想不到的冲击  相似文献   

Phosphorus solubility mechanisms in haplogranitic aluminosilicate glass and melt: effect of temperature and aluminum content   总被引：1，自引：0，他引：1  

Bjorn O. Mysen 《Contributions to Mineralogy and Petrology》1998,133(1-2):38-50

The solubility behavior of phosphorus in glasses and melts in the system Na₂O-Al₂O₃-SiO₂-P₂O₅ has been examined as a function of temperature and Al₂O₃ content with microRaman spectroscopy. The Al₂O₃ was added (2, 4, 5, 6, and 8 mol% Al₂O₃) to melts with 80 mol% SiO₂ and ∼2 mol% P₂O₅. The compositions range from peralkaline, via meta-aluminous to peraluminous. Raman spectra were obtained of both the phosphorus-free and phosphorous-bearing glasses and melts between 25 and 1218 °C. The Raman spectrum of Al-free, P-bearing glass exhibits a characteristic strong band near 940 cm⁻¹ assigned to P=O stretching in orthophosphate complexes together with a weaker band near 1000 cm⁻¹ assigned P₂O₇ complexes. With increasing Al content, the proportion of P₂O₇ initially increases relative to PO₄ and is joined by AlPO₄ complexes which exhibit a characteristic P-O stretch mode slightly above 1100 cm⁻¹. The latter complex appears to dominate in meta-aluminosilicate glass and is the only phosphate complex in peraluminous glasses. When P-bearing peralkaline silicate and aluminosilicate glasses are transformed to supercooled melts, there is a rapid decrease in PO₄/P₂O₇ so that in the molten state, PO₄ units are barely discernible. The P₂O₇/AlPO₄ abundance ratio in peralkaline compositions increases with increasing temperature. This decrease in PO₄/P₂O₇ with increasing temperature results in depolymerization of the silicate melts. Dissolved P₂O₅ in peraluminous glass and melts forms AlPO₄ complexes only. This solution mechanism has no discernible influence on the aluminosilicate melt structure. There is no effect of temperature on this solution mechanism. Received: 7 October 1997 / Accepted: 11 May 1998  相似文献   

An Improved Method for Modeling Spatial Distribution of δD in Surface Snow over Antarctic Ice Sheet   总被引：1，自引：1，他引：0  

Yetang Wang  Shugui Hou  Bjorn Grigholm  Linlin Song 《中国地理科学(英文版)》2009,19(2):120-125

Using the recent compilation of the isotopic composition data of surface snow of Antarctic ice sheet, we proposed an improved interpolation method of δD, which utilizes geographical factors (i.e., latitude and altitude) as the primary predictors and incorporates inverse distance weighting (IDW) technique. The method was applied to a high-resolution digital elevation model (DEM) to produce a grid map of multi-year mean δD values with 1km spatial resolution for Antarctic& The mean absolute deviation between observed and estimated data in the map is about 5.4‰, and the standard deviation is 9‰. The resulting δD pattern resembles well known characteristics such as the depletion of the heavy isotopes with increasing latitude and distance from coast line, but also reveals the complex topographic effects.  相似文献