Mineral dissolution in the Cape Cod aquifer, Massachusetts, USA: I . Reaction stoichiometry and impact of accessory feldspar and glauconite on strontium isotopes, solute concentrations, and REY distribution     

Michael Bau  Brian Alexander  John T Chesley  Susan L Brantley 《Geochimica et cosmochimica acta》2004,68(6):1199-1216

To compare relative reaction rates of mineral dissolution in a mineralogically simple groundwater aquifer, we studied the controls on solute concentrations, Sr isotopes, and rare earth element and yttrium (REY) systematics in the Cape Cod aquifer. This aquifer comprises mostly carbonate-free Pleistocene sediments that are about 90% quartz with minor K-feldspar, plagioclase, glauconite, and Fe-oxides. Silica concentrations and pH in the groundwater increase systematically with increasing depth, while Sr isotopic ratios decrease. No clear relationship between ⁸⁷Sr/⁸⁶Sr and Sr concentration is observed. At all depths, the ⁸⁷Sr/⁸⁶Sr ratio of the groundwater is considerably lower than the Sr isotopic ratio of the bulk sediment or its K-feldspar component, but similar to that of a plagioclase-rich accessory separate obtained from the sediment. The Si-⁸⁷Sr/⁸⁶Sr-depth relationships are consistent with dissolution of accessory plagioclase. In addition, solutes such as Sr, Ca, and particularly K show concentration spikes superimposed on their respective general trends. The K-Sr-⁸⁷Sr/⁸⁶Sr systematics suggests that accessory glauconite is another major solute source to Cape Cod groundwater. Although the authigenic glauconite in the Cape Cod sediment is rich in Rb, it is low in in-grown radiogenic ⁸⁷Sr because of its young Pleistocene age. The low ⁸⁷Sr/⁸⁶Sr ratios are consistent with equilibration of glauconite with seawater. The impact of glauconite is inferred to vary due to its variable abundance in the sediments. In the Cape Cod groundwater, the variation of REY concentrations with sampling depth resembles that of K and Rb, but differs from that of Ca and Sr. Shale-normalized REY patterns are light REY depleted, show negative Ce anomalies and super-chondritic Y/Ho ratios, but no Eu anomalies. REY input from feldspar, therefore, is insignificant compared to input from a K-Rb-bearing phase, inferred to be glauconite. These results emphasize that interpretation of groundwater chemistry, even in relatively simple aquifers, may be complicated by solute contributions from “exotic” accessory minerals such as glauconite. To detect such peculiarities, groundwater studies should combine the study of elemental concentration and isotopic composition of several solutes that show different geochemical behavior.  相似文献   

Iodine-xenon analysis of ordinary chondrite halide: implications for early solar system water     

A Busfield  J.D Gilmour  G Turner 《Geochimica et cosmochimica acta》2004,68(1):195-202

We report the results of iodine-xenon analyses of irradiated halide grains extracted from the H-chondrite Monahans (1998) and compare them with those from Zag (Whitby et al., 2000) to address the timing of aqueous processing on the H-chondrite parent body. Xe isotopic analyses were carried out using the RELAX mass spectrometer with laser stepped heating. The initial ¹²⁹I/¹²⁷I ratio in the Monahans halide was determined to be (9.37 ± 0.06) × 10⁻⁵ with an iodine concentration of ∼400 ppb. Significant scatter, especially in the Zag data, indicates that a simple interpretation as a formation age is unreliable. Instead we propose a model whereby halide minerals in both meteorites formed ∼5 Ma after the enstatite achondrite Shallowater (at an absolute age of 4559 Ma). This age is in agreement with the timing of aqueous alteration on the carbonaceous chondrite parent bodies and ordinary chondrite metamorphism and is consistent with the decay of ²⁶Al as a heat source for heating and mobilisation of brines on the H-chondrite parent body. Post accretion surface impact events may have also contributed to the heat source.  相似文献   

Estimating severity of liquefaction-induced damage near foundation   总被引：1，自引：2，他引：1  

C. Hsein Juang  Haiming Yuan  David Kun Li  Susan Hui Yang  Raymond A. Christopher 《Soil Dynamics and Earthquake Engineering》2005,25(5):403-411

An empirical procedure for estimating the severity of liquefaction-induced ground damage at or near foundations of existing buildings is established. The procedure is based on an examination of 30 case histories from recent earthquakes. The data for these case histories consist of observations of the damage that resulted from liquefaction, and the subsurface soil conditions as revealed by cone penetration tests. These field observations are used to classify these cases into one of three damaging effect categories, ‘no damage’, ‘minor to moderate damage’, and ‘major damage’. The potential for liquefaction-induced ground failure at each site is calculated and expressed as the probability of ground failure. The relationship between the probability of ground failure and the damage class is established, which allows for the evaluation of the severity of liquefaction-induced ground damage at or near foundations. The procedure presented herein represents a significant attempt to address the issue of liquefaction effect. Caution must be exercised, however, when using the proposed model and procedure for estimating liquefaction damage severity, because they are developed based on limited number of case histories.  相似文献   

Geomagnetism and Schmidt quasi-normalization     

D. E. Winch  D. J. Ivers  J. P. R. Turner  R. J. Stening 《Geophysical Journal International》2005,160(2):487-504

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Production of a molybdophore during metal-targeted dissolution of silicates by soil bacteria   总被引：1，自引：0，他引：1  

Laura J. Liermann  Robin L. Guynn  Ariel Anbar  Susan L. Brantley   《Chemical Geology》2005,220(3-4):285-302

Although many bioessential metals are scarce in natural water and rock systems, microbial secretion of high-affinity ligands for metal extraction from solid phases has only been documented for Fe. However, we have discovered that Mo is extracted from a silicate by a high-affinity ligand (a possible “molybdophore”) secreted by an N₂-fixing soil bacterium. The putative molybdophore, aminochelin, is secreted as a siderophore under Fe-depleted conditions, but is also secreted under Fe-sufficient, Mo-depleted conditions. Presumably, molybdophore production facilitates uptake of Mo for use in Mo enzymes. In contrast, an Fe-requiring soil bacterium without a special Mo requirement only enhances the release of Fe from the silicate. Fractionation of Mo stable isotopes during uptake to cells may provide a “fingerprint” for the importance of chelating ligands in such systems. Many such metal-specific ligands secreted by prokaryotes for extraction of bioessential metals, their effects on Earth materials, and their possible utility in the recovery of economic metals remain to be discovered.  相似文献   

A Modified Terzaghi Consolidation Factor for First-Order Estimation of Overpressure Resulting From Sedimentation: Review and Synthesis   总被引：1，自引：0，他引：1  

Susan Ellis  David Darby 《Mathematical Geology》2005,37(1):115-123

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Tetrahedral Plots of the Phase Relations for Basalts     

Sven Maal?e  Richard N. Abbott Jr. 《Mathematical Geology》2005,37(8):869-893

The phase relations of quaternary systems are generally represented by projections onto ternary compositional planes. Such projections often obscure relationships that would only be evident in a three-dimensional tetrahedral plot. The tetrahedral plot requires that compositions of the minerals and melts be transformed into Cartesian coordinates. It is shown here how this transformation is carried out. The application is demonstrated by tetrahedral plots of experimental melt compositions of partially molten lherzolite. Furthermore, the plot can be used to evaluate whether or not a particular basaltic composition represents a primary melt. The methods are applicable to any four-component system.  相似文献   

Iodine-xenon analysis of Chainpur (LL3.4) chondrules     

G. Holland  J.C. Bridges  A. Busfield  G. Turner 《Geochimica et cosmochimica acta》2005,69(1):189-200

We present I-Xe analyses of ten chondrules from Chainpur LL3.4 by IR laser-stepped heating. Five chondrules provided isochrons of varying quality, giving a range of ages from 0.5 Ma before Shallowater to 17.8 after Shallowater. This confirms the extended range of Chainpur chondrule ages determined by previous data. We discuss evidence for fluid alteration, shock, and thermal events in explaining the chondrule ages and suggest that chondrule remelting events, presumably from bombardment of the parent body surface, are responsible for resetting the I-Xe chronometer. Previous data show a negative correlation between ¹³²Xe/¹²⁹Xe of the trapped Xe component and ¹²⁷I/¹²⁹I of an initial iodine component. This behaviour that requires the presence of a component with trapped ¹²⁹Xe/¹³²Xe lower than the planetary value has been cited as evidence for closed system evolution of the I-Xe system. We find no evidence of an unambiguous trapped component lower than planetary and no evidence of a negative correlation in our data. Therefore we suggest that open system behaviour more suitably explains the I-Xe systematics of Chainpur chondrules.  相似文献   

Negative δO values in Allan Hills 84001 carbonate: Possible evidence for water precipitation on mars     

G. Holland  J.M. Saxton  G. Turner 《Geochimica et cosmochimica acta》2005,69(5):1359-1370

The Martian meteorite ALH84001 contains ∼1% by weight of carbonate formed by secondary processes on the Martian surface or in the shallow subsurface. The major form of this carbonate is chemically and isotopically zoned rosettes which have been well documented elsewhere. This study concentrates upon carbonate regions ∼200 μm across which possess previously unobserved magnesium rich inner cores, interpreted here as rosette fragments, surrounded by a later stage cement containing rare Ca-rich carbonates (up to Ca₈₁Mg₀₇Fe₀₄Mn₀₇) intimately associated with feldspar. High spatial resolution ion probe analyses of Ca-rich carbonate surrounding rosette fragments have δ¹⁸O_V-SMOW values as low as −10‰. These values are not compatible with deposition from a global Martian atmosphere invoked to explain ALH84001 rosettes. The range of δ¹⁸O values are also incompatible with a fluid that has equilibrated with the Martian crust at high temperature or from remobilisation of carbonate of rosette isotopic composition. At Martian atmospheric temperatures, the small CO₂(gas)-CO₂(ice) fractionation makes meteoric CO₂ an unlikely source for −10‰ carbonates. In contrast, closed system Rayleigh fractionation of H₂O can generate δ¹⁸O_H2O −30‰, as observed at high latitudes on Earth. We suggest that atmospheric transport and precipitation of H₂O in a similar fashion to that on Earth provides a source of suitably ¹⁸O depleted water for generation of carbonate with δ¹⁸O_V-SMOW = −10‰.  相似文献   

On the Sr isotope and REE compositions of anhydrites from the TAG seafloor hydrothermal system   总被引：1，自引：0，他引：1  

Susan E. Humphris  Wolfgang Bach 《Geochimica et cosmochimica acta》2005,69(6):1511-1525

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