再论各向异性介质转换波地震学,第一部分:理论     

Xiangyang Li  Jianxin Yuan British Geological Survey  West Mains Road  Edinburgh EH LA  UK. Formerly at British Geological Survey  now at PGS Inc.  Richmond Avenue  Suite  Houston  TX  USA. 《应用地球物理》2005,2(1)

我们业已研发了计算各向异性、非均质介质中P- SV转换波(C-波)的转换点和旅行时的新理论。据此 可以利用诸如相似性分析、迪克斯模型建模、克契 霍夫求和等常规方法来完成各向异性的处理和各向 异性处理,并使各向异性的处理成为可能。这里将 我们的新发展分作两部分来介绍。第一部分为理 论,第二部分为对速度分析和参数计算的应用。第 一部分理论包括转换点的计算和动校正的分析。  相似文献   

Location and quantitative analysis of OH in coesite     

M. Koch-Müller  Y. Fei  E. Hauri  Z. Liu 《Physics and Chemistry of Minerals》2001,28(10):693-705

 The incorporation of hydrogen (deuterium) into the coesite structure was investigated at pressures from 3.1 to 7.5 GPa and temperatures of 700, 800, and 1100 °C. Hydrogen could only be incorporated into the coesite structure at pressures greater 5.0 GPa and 1100 °C . No correlation between the concentration of trace elements such as Al and B and the hydrogen content was observed based on ion probe analysis (1335 ± 16 H ppm and 17 ± 1 Al ppm at 7.5 GPa, 1100 °C). The FTIR spectra show three relatively intense bands at 3575, 3516, and 3459 cm⁻¹ (ν₁ to ν₃, respectively) and two very weak bands at 3296 and 3210 cm⁻¹ (ν₄ and ν₅, respectively). The band at 3516 cm⁻¹ is strongly asymmetric and can be resolved into two bands, 3528 (ν_2a) and 3508 (ν_2b) cm⁻¹, with nearly identical areas. Polarized infrared absorption spectra of coesite single-crystal slabs, cut parallel to (0 1 0) and (1 0 0), were collected to locate the OH dipoles in the structure and to calibrate the IR spectroscopy for quantitative analysis of OH in coesite (ɛ _{i ,tot}=190 000 ± 30 000 l mol⁻¹ _H2O cm⁻²). The polarized spectra revealed a strong pleochroism of the OH bands. High-pressure FTIR spectra at pressures up to 8 GPa were performed in a diamond-anvil cell to gain further insight into incorporation mechanism of OH in coesite. The peak positions of the ν₁, ν₂, and ν₃ bands decrease linearly with pressure. The mode Grüneisen parameters for ν₁, ν₂, and ν₃ are −0.074, −0.144 and −0.398, respectively. There is a linear increase of the pressure derivatives with band position which follows the trend proposed by Hofmeister et al. (1999). The full widths at half maximum (FWHM) of the ν₁, ν₂, and ν₃ bands increase from 35, 21, and 28 cm⁻¹ in the spectra at ambient conditions to 71, 68, and 105 in the 8 GPa spectra, respectively. On the basis of these results, a model for the incorporation of hydrogen in coesite was developed: the OH defects are introduced into the structure by the substitution Si^4+(Si2)+4O²⁻= ^[4]□^(Si2) + 4OH⁻, which gives rise to four vibrations, ν₁, ν_2a, ν_2b, and ν₃. Because the OH(D)-bearing samples do contain traces of Al and B, the bands ν₄ and ν₅ may be coupled to Al and/or B substitution. Received: 19 December 2000 / Accepted: 23 April 2001  相似文献   

Volatile loss from melt inclusions in pyroclasts of differing sizes     

Alexander S. Lloyd  Terry Plank  Philipp Ruprecht  Erik H. Hauri  William Rose 《Contributions to Mineralogy and Petrology》2013,165(1):129-153

We have investigated the loss of H₂O from olivine-hosted melt inclusions (MIs) by designing an experiment using tephra samples that cooled at different rates owing to their different sizes: ash, lapilli, and bomb samples that were deposited on the same day (10/17/74) of the sub-Plinian eruption of Volcán de Fuego in Guatemala. Ion microprobe, laser ablation-ICPMS, and electron probe analyses show that MIs from ash and lapilli record the highest H₂O contents, up to 4.4 wt%. On the other hand, MIs from bombs indicate up to 30 % lower H₂O contents (loss of ~1 wt% H₂O) and 10 % post-entrapment crystallization of olivine. This evidence is consistent with the longer cooling time available for a bomb-sized clast, up to 10 min for a 3–4-cm radius bomb, assuming conductive cooling and the fastest H diffusivities measured in olivine (D~10^?9 to 10^?10 m²/s). On the other hand, several lines of evidence point to some water loss prior to eruption, during magma ascent and degassing in the conduit. Thus, results point to both slower post-eruptive cooling and slower magma ascent affecting MIs from bombs, leading to H₂O loss over the timescale of minutes to hours. The important implication of this study is that a significant portion of the published data on H₂O concentrations in olivine-hosted MIs may reflect unrecognized H₂O loss via diffusion. This work highlights the importance of reporting clast and MI sizes in order to assess diffusive effects and the potential benefit of using water loss as a chronometer of magma ascent.  相似文献   

Lithium isotope systematics of lavas from the Cook–Austral Islands: Constraints on the origin of HIMU mantle     

Lui-Heung Chan  John C. Lassiter  Erik H. Hauri  Stanley R. Hart  Jerzy Blusztajn 《Earth and Planetary Science Letters》2009,277(3-4):433-442

Radiogenic isotope variations in lavas from the Cook–Austral volcanic chain have delineated three distinct mantle sources: a HIMU component, a depleted component (DM), and an enriched component (EM). To better constrain the mantle sources for South Pacific hot spot volcanism, we determined lithium isotopic compositions of lavas from Raivavae, Rapa, Mangaia and Tubuai of the volcanic chain. The study includes whole rock and mineral analyses. In general, δ⁷Li of most olivines resemble bulk rock composition whereas clinopyroxenes are variably lighter. This implies that clinopyroxene is more susceptible to diffusion-induced fractionation, in agreement with previous studies. Olivine δ⁷Li values span a narrower range than whole rock values, and do not extend to the very heavy compositions previously reported in HIMU bulk lavas. This discrepancy likely reflects alteration of bulk lavas, and suggests that Li-isotope analyses of bulk lavas should be interpreted with caution. Olivines from HIMU lavas have heavy δ⁷Li values (up to 6.2‰), and extend beyond the range reported for fresh MORB. Correlations between Li-isotopes and radiogenic isotopes suggest that the heavy δ⁷Li values in HIMU olivines are a source characteristic and not the result of post-magmatic alteration. Although the Li-isotope composition of recycled, dehydrated oceanic crust is currently under debate, our results suggest that HIMU lavas derive from a source containing recycled dehydrated oceanic crust, and that the “heavy” Li-isotope signature of altered oceanic crust is partially preserved during passage through the subduction factory.  相似文献   

H<Subscript>2</Subscript>O solubility in basalt at upper mantle conditions     

Alexandra?L.?MitchellEmail author  Glenn?A.?Gaetani  Julie?A.?O’Leary  Erik?H.?Hauri 《Contributions to Mineralogy and Petrology》2017,172(10):85

This study presents a new experimental approach for determining H₂O solubility in basaltic melt at upper mantle conditions. Traditional solubility experiments are limited to pressures of ~600 MPa or less because it is difficult to reliably quench silicate melts containing greater than ~10 wt% dissolved H₂O. To overcome this limitation, our approach relies on the use of secondary ion mass spectrometry to measure the concentration of H dissolved in olivine and on using the measured H in olivine as a proxy for the concentration of H₂O in the co-existing basaltic melt. The solubility of H₂O in the melt is determined by performing a series of experiments at a single pressure and temperature with increasing amounts of liquid H₂O added to each charge. The point at which the concentration of H in the olivine first becomes independent of the amount of initial H₂O content of the charge (added + adsorbed H₂O) indicates its solubility in the melt. Experiments were conducted by packing basalt powder into a capsule fabricated from San Carlos olivine, which was then pressure-sealed inside a Ni outer capsule. Our experimental results indicate that at 1000 MPa and 1200 °C, the solubility of H₂O in basaltic melt is 20.6 ± 0.9 wt% (2 × standard deviation). This concentration is considerably higher than predicted by most solubility models but defines a linear relationship between H₂O fugacity and the square of molar H₂O solubility when combined with solubility data from lower pressure experiments. Further, our solubility determination agrees with melting point depression determined experimentally by Grove et al. (2006) for the H₂O-saturated peridotite solidus at 1000 MPa. Melting point depression calculations were used to estimate H₂O solubility in basalt along the experimentally determined H₂O-saturated peridotite solidus. The results suggest that a linear relationship between H₂O fugacity and the square of molar solubility exists up to ~1300 MPa, where there is an inflection point and solubility begins to increase less strongly with increasing H₂O fugacity.  相似文献   

A petrogenetic model for the comagmatic origin of chassignites and nakhlites: Inferences from chlorine‐rich minerals,petrology, and geochemistry     

Francis M. McCubbin  Stephen M. Elardo  Charles K. Shearer Jr.  Alexander Smirnov  Erik H. Hauri  David S. Draper 《Meteoritics & planetary science》2013,48(5):819-853

Twelve samples belonging to the chassignite and nakhlite subgroups of Martian meteorites were investigated using a variety of micro‐beam analytical techniques to gain insight into the petrogenesis of these two meteorite classes. There are a striking number of geochemical similarities between the chassignites and nakhlites, including mineralogy and petrology, crystallization age, cosmic‐ray exposure age, and radiogenic isotopic compositions. However, there are also geochemical differences, namely in trace element systematics of pyroxenes, that have led some authors to conclude that the nakhlites are comagmatic with each other, but not comagmatic with the chassignites. On the basis of data presented here, we propose a model in which these differences can be reconciled by the addition of an exogenous Cl‐rich fluid to the chassignite‐nakhlite magma body shortly after the formation of the cumulate horizon that was sampled by the Chassigny meteorite. This model is supported by the textural and chemical associations of the volatile‐bearing minerals apatite, amphibole, and biotite, which record a history starting with the addition of a Cl‐ and LREE‐enriched fluid to the magma body. As the magma continued to crystallize, it eventually reached chloride saturation and degassed a Cl‐rich fluid phase. Depending on the provenance of the Cl‐rich fluid, this model could explain how the chassignites and nakhlites originated from an LREE‐depleted source, yet all exhibit LREE‐enriched bulk‐rock patterns. Additionally, the model explains the range in oxygen fugacity that is recorded by the chassignites and nakhlites because eventual exsolution and loss of Cl‐rich fluid phases near the end of crystallization of the nakhlite sequence leads to auto‐oxidation of the magma body due to the preferential partitioning of Fe²⁺ into the fluid phase.  相似文献   

Magma decompression rates during explosive eruptions of Kīlauea volcano,Hawaii, recorded by melt embayments     

David J. Ferguson  Helge M. Gonnermann  Philipp Ruprecht  Terry Plank  Erik H. Hauri  Bruce F. Houghton  Donald A. Swanson 《Bulletin of Volcanology》2016,78(10):71

  相似文献   

High precision iron isotope measurements of meteoritic material by cold plasma ICP-MS   总被引：1，自引：0，他引：1  

K Kehm  E.H Hauri  R.W Carlson 《Geochimica et cosmochimica acta》2003,67(15):2879-2891

The first cold plasma ICP-MS (inductively coupled plasma mass spectrometer) Fe isotope study is described. Application of this technique to the analyses of Fe isotopes in a number of meteorites is also reported. The measurement technique relies on reduced temperature operation of the ICP source to eliminate pervasive molecular interferences from Ar complexes associated with conventional ICP-MS. Instrumental mass bias corrections are performed by sample-standard bracketing and using Cu as an external mass bias drift monitor. Repeated measurements of a terrestrial basalt reference sample indicate an external reproducibility of ± 0.06 ‰ for δ⁵⁶Fe and ± 0.25 ‰ for δ⁵⁸Fe (1 σ). The measured iron isotopic compositions of various bulk meteorites, including irons, chondrites and pallasites are identical, within error, to the composition of our terrestrial basalt reference sample suggesting that iron mass fractionation during planet formation and differentiation was non-existent. Iron isotope compositions measured for eight chondrules from the unequilibrated ordinary chondrite Tieschitz range from −0.5 ‰ < δ⁵⁶Fe_chondrules < 0.0 ‰ relative to the terrestrial/meteorite average. Mechanisms for fractionating iron in these chondrules are discussed.  相似文献   

Mantle fluid evolution—a tale of one diamond     

Ofra Klein-BenDavid  Elad S. Izraeli  Erik Hauri  Oded Navon 《Lithos》2004,77(1-4):243-253

Microinclusions analyzed in a coated diamond from the Diavik mine in Canada comprise peridotitic minerals and fluids. The fluids span a wide compositional range between a carbonatitic melt and brine. The diamond is concentrically zoned. The brine microinclusions reside in an inner growth zone and their endmember composition is K₁₉Na₂₅Ca₅Mg₈Fe₃Ba₂Si₄Cl₃₂ (mol%). The carbonatitic melt is found in an outer layer and its endmember composition is K₁₁Na₂₁Ca₁₁Mg₂₆Fe₇Ba₂Si₁₀Al₃P₂Cl₅. The transition in inclusion chemistry is accompanied by a change in the carbon isotopic composition of the diamond from −8.5‰ in the inner zone to −12.1‰ in the outer zone. We suggest that this transition reflects mixing between already evolved brine and a freshly introduced carbonatitic melt of different isotopic composition.

The compositional range found in diamond ON-DVK-294 is the widest ever recorded in a single diamond. It closes the gap between brine found in cloudy octahedral diamonds from South Africa and carbonatitic melt analyzed in cubic diamonds from Zaire and Botswana. Thus, all microinclusions analyzed to date fall along two arrays connecting the carbonatitic melt composition to either a hydrous-silicic endmember or to a brine endmember. This connection suggests that many diamonds are formed from fluids derived form a mantle source not significantly influenced by local heterogeneities.  相似文献   

Diffusive fractionation of U-series radionuclides during mantle melting and shallow-level melt-cumulate interaction     

James A. Van Orman  Alberto E. Saal  Erik H. Hauri 《Geochimica et cosmochimica acta》2006,70(18):4797-4812

U-series radioactive disequilibria in basaltic lavas have been used to infer many important aspects of melt generation and extraction processes in Earth’s mantle and crust, including the porosity of the melting zone, the solid mantle upwelling rate, and the melt transport rate. Most of these inferences have been based on simplified theoretical treatments of the fractionation process, which assume equilibrium partitioning of U-series nuclides among minerals and melt. We have developed a numerical model in which solid-state diffusion controls the exchange of U-series nuclides among multiple minerals and melt. First the initial steady-state distribution of nuclides among the phases, which represents a balance between diffusive fluxes and radioactive production and decay, is calculated. Next, partial melting begins, or a foreign melt is introduced into the system, and nuclides are again redistributed among the phases via diffusion. U-series nuclides can be separated during this stage due to differences in their diffusivity; radium in particular, and possibly protactinium as well, can be strongly fractionated from slower-diffusing thorium and uranium. We show that two distinct processes are not required for the generation of ²²⁶Ra and ²³⁰Th excesses in mid-ocean ridge basalts, as has been argued previously; instead the observed negative correlations of the (²²⁶Ra/²³⁰Th) activity ratio with (²³⁰Th/²³⁸U) and with the extent of trace element enrichment may result from diffusive fractionation of Ra from Th during partial melting of the mantle. Alternatively, the (²²⁶Ra/²³⁰Th) disequilibrium in mid-ocean ridge basalts may result from diffusive fractionation during shallow-level interaction of mantle melts with gabbroic cumulates, and we show that the results of the interaction have a weak dependence on the age of the cumulate if both plagioclase and clinopyroxene are present.  相似文献