December 2004 (second edition)     

Peter Warneck 《Environmental Geology》2003,45(2):294-294

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Volkmar Trommsdorff  George Skippen  Peter Ulmer 《Contributions to Mineralogy and Petrology》1985,89(1):24-29

Solid inclusions of halite and sylvite, formed during regional and contact metamorphism have been identified by microscopy and by electron microprobe analysis in rocks from Campolungo, Switzerland and Cornone di Blumone, Italy. The solid inclusions occur in several of the major minerals crystallized during metamorphism and have been observed as idiomorphic crystals and dendrites. The compositions measured in 100 analyses from Campolungo, Switzerland and 40 analyses from Cornone di Blumone, Italy extend across the two-phase region in the system, KCl-NaCl, indicating that the salt inclusions are high temperature precipitates. In both localities compositionally zoned and unzoned crystals have been found. Measured compositions on the temperature maximum of the two-phase region indicate at least 500° C which can be compared with 500°±20° C determined by Mercolli (1982) and Walther (1983) from the Mg content of calcites from Campolungo. The solid inclusions have been trapped apart from CO₂-rich and saline, H₂O-rich fluid inclusions which have been described by Mercolli (1982) as the earliest preserved fluid inclusions in the rocks. The early precipitation of salt minerals at Campolungo indicates that fluids were saturated with NaCl and KCl at 500° C and pressures of 2,000 bars or higher. Similar relationships exist between solid and fluid inclusions in the rocks of Cornone di Blumone which formed at temperatures as high as 800° C and pressures between 0.5 and 1 kilobar (Ulmer 1983). The entrapment of halite and sylvite as solid inclusions preserves the composition of the minerals which may therefore be useful as geothermometers.  相似文献   

    

Kazushige Tomeoka  Peter R. Buseck 《Geochimica et cosmochimica acta》1985,49(10):2149-2163

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Gaspar  Jose C.  Wyllie  Peter J. 《Contributions to Mineralogy and Petrology》1984,85(2):133-140

Carbonate-rich, SiO₂-poor residua are developed in some kimberlites solidifying as ocelli, layers, or discrete dikes which satisfy petrographic definitions of carbonatite. Arguments that these rocks have mineralogies, antecedents, and comagmatic rocks differing from those of the carbonatites in alkaline rock complexes, including the specific observation that kimberlites and carbonatites contain ilmenites and spinels of different composition, have been used to refute the alleged kimberlite-carbonatite relationship. New microprobe analyses of ilmenites and spinels from carbonate-rich rocks associated with kimberlites in three South African localities correspond to spinels and ilmenites of carbonatites from alkalic complexes, or have characteristics intermediate between those of carbonatites and kimberlites. The ilmenites are distinguished from kimberlite ilmenites by higher MnO, FeTiO₃, and Nb₂O₅, and by negligible Cr₂O₃. The spinels are distinguished from kimberlite spinels by their Al₂O₃ and Cr₂O₃ contents. There is clearly a genetic relationship between the kimberlites and the carbonate-rich rocks, despite the observation that their ilmenites and spinels are distinctly different, which indicates that the same observation is not a valid argument against a petrogenetic relationship between kimberlites and carbonatites. These rocks are among the diverse products from mantle processes influenced by CO₂, and we believe that the petrogenetic links among them are forged in the upper mantle. We see insufficient justification to deny the name carbonatite to carbonate-rich rocks associated with kimberlites if they satisfy the petrographic definition in terms of major mineralogy.  相似文献   

    

Urs P Nyffeler  Yuan-Hui Li  Peter H Santschi 《Geochimica et cosmochimica acta》1984,48(7):1513-1522

The partitioning of radioactive trace elements between seawater and particulate matter from surface sediments and sediment traps was investigated in laboratory experiments. For the elements Na, Zn, Se, Sr, Cd, Sn, Sb, Cs, Ba, Hg, Th and Pa (group I) constant distribution coefficients (K_d) were found after a few days of equilibration, whereas the elements Be, Mn, Co and Fe (group II) showed an increasing K_d over the whole time of observation of 108 days. The time dependence of K_d is described by an adsorption-desorption equilibrium (group I elements), followed by a lattice transport reaction step (group II elements). The reaction rate constants are compared to Mn oxidation rates and to adsorption rate constants derived from in situ measurements of the $\text{U}\text{Th}$ disequilibrium as available from literature.  相似文献   

  总被引：6，自引：0，他引：6  

L.Peter Gromet  Larry A. Haskin  Randy L. Korotev  Robert F. Dymek 《Geochimica et cosmochimica acta》1984,48(12):2469-2482

The compilation and major element composition of the “North American shale composite” (NASC) are reported for the first time, along with redeterminations for the REE and selected other elements by modern, high precision analytical methods. The NASC is not strictly of North American origin; 5 of the constituent samples are from Africa and Antarctica, and 15 are from unspecified locations. The major element composition of the NASC compares quite closely with other average shale compositions. New analyses of the NASC document that significant portions of the REE and some other trace elements are contained in minor phases (zircon and possibly other minerals) and that their uneven distribution in the NASC powder appears to have resulted in heterogeneity among analyzed aliquants. The results of this study show that the REE distributions of detrital sediments can be dependent to some extent on their minor mineral assemblages and the sedimentological factors that control these assemblages. Consequently, caution should be exercised in the interpretation of the REE distributions of sediment samples as they may be variable and biased relative to average REE distribution of the crustal rocks supplying detritus. These effects appear to be largely averaged out in sediment composites, with the result that their REE distributions are more likely to be representative of their provenances.  相似文献   

    

Peter J. Mehringer  John C. Sheppard  Franklin F. Foit 《Quaternary Research》1984,21(1):36-41

At Sheep Mountain Bog, near Missoula, Montana, a late-glacial tephra, that probably fell in late summer, is preserved as an 8-mm-thick graded bed overlain by another 8 mm of redeposited ash mixed with lake deposits. Sediment surrounding the ash was ¹⁴C dated to about 11,200 yr B.P. Electron-microprobe analyses of the volcanic glass and hornblende phenocrysts from this ash layer indicate that they are similar in major-element chemistry to those of Glacier Peak layer G previously considered to be about 12,000 yr old or older.  相似文献   

    

Jean M. RICHARDSON  Peter C. LIGHTFOOT  Hugh de  SOUZA 《Geostandards and Geoanalytical Research》1996,20(1):141-156

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Stephen B. Weisberg  Peter Himchak  Tom Baum  Harold T. Wilson  Russell Allen 《Estuaries and Coasts》1996,19(3):723-729

Water quality in the tidal Delaware River has improved dramatically over the last several decades. Areas near Philadelphia that were once anoxic and formed a pollution block to migratory fish passage now rarely experience dissolved oxygen concentrations less than 3 ppm. To assess whether these improvements in water quality led to increased abundance of juvenile fishes, data from a beach seine survey conducted annually since 1980 were examined. The number of species captured increased throughout the tidal river, but the increase was greatest in the areas downstream of Philadelphia, wheare water quality has improved the most. Abundance of juvenile striped bass and American shad, two important game species in the river whose migratory patterns make them susceptible to water quality problems, both increased more than, 1,000-fold during the last decade. Correlatations between the temporal abundance patterns of these species in the tidal Delaware River and in other East Coast systems were poor, suggesting that increases in their numbers were related more closely to improving conditions within the Delaware than to factors affecting coastal stocks.  相似文献   

    

Peter G. Burnard  David A. Polya 《Geochimica et cosmochimica acta》2004,68(7):1607-1615

Helium trapped in arsenopyrite and wolframite from the Panasqueira hydrothermal deposit in central Portugal is overwhelmingly—≈ 75%—derived from the mantle. This is surprising as the W-Cu(Ag)-Sn vein deposits are spatially and temporally associated with an S-type granite. It is difficult to reconcile ³He/⁴He ratios > 5Ra (where Ra is the atmospheric ³He/⁴He ratio) with a granite produced by crustal anatexis, therefore it seems likely that mantle derived fluids unrelated to the granite were the source of the magmatic component in the ore fluids.The mantle appears to transport ³He and heat to the surface in relatively constant proportions (³He/Q = 0.1-1 x10⁻¹² cm³ STP J⁻¹). However, the ³He/heat ratios in the Panasqueira fluids (1-10 x10⁻¹² cm³ STP J⁻¹, calculated using the ³He/³⁶Ar ratio) are considerably higher. Therefore, it does not seem likely that gradual cooling of the pluton supplied heat to the hydrothermal system (as this would result in low ³He/Q ratios). Therefore, both He and heat in this collision related, granite-associated hydrothermal deposit were supplied from the mantle.  相似文献