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1.
The 87Sr86Sr ratios of several oilfield brines associated with Paleozoic dolomites, cherty dolomites and sandstones from Kansas and Colorado range from 0.7113 to 0.7341. Two brines in the Mississippian dolomites from Colorado were found to contain the most radiogenic strontium. The 87Sr86Sr ratios of brines in a small oilfield in eastern Kansas are constant, and the ratios may suggest that in this field there may be only one oil pool. The isotopic composition of strontium in subsurface waters could be useful in determining hydrologic continuity among reservoirs and for obtaining additional information on the origin and migration of these fluids.  相似文献   

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The South Mountain batholith of southwestern Nova Scotia is a large, peraluminous, granodiorite-granite complex which intrudes mainly greenschist facies metasediments of the Cambro-Ordovician Meguma Group. Using Rb-Sr isochrons constructed from whole rocks and mineral separates, the present study shows a variation in age and initial ratios of the intrusive phases of the batholith as follows: biotite granodiorite (371.8 ± 2.2 Ma, (87Sr86Sr)i ranges from 0.7076 ± 0.0003 to 0.7090 ± 0.0003, with the average = 0.7081); adamellite (364.3 ± 1.3 Ma, (87Sr86Sr)i = 0.70942 ± 35); porphyry (361.2 ± 1.4 Ma, (87Sr86Sr)i = 0.71021 ± 119); using λ87Rb = 1.42 × 10?11yr?1.A suite of Meguma country rock samples showed a variation of 87Sr86Sr = 0.7113?0.7177 at the time of intrusion of the batholith. A number of xenoliths of this material occurring in the marginal granodiorite had partially equilibrated isotopically with the granodiorite at a higher 87Sr86Sr ratio than elsewhere in the granodiorites. This evidence demonstrates that isotopic (and probably some accompanying bulk chemical) contamination by the Meguma rocks has been an important factor in determining the ultimate chemical composition and mineralogy of the South Mountain batholith.The (87Sr86Sr)372 = 0.7081 of the early granodiorites indicates that the parent magma of the South Mountain batholith was derived from a source unlike the Meguma Group. The precise nature of the source region cannot be determined by Rb-Sr work unless the degree of contamination with Megumalike material is known.  相似文献   

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Pleistocene and Recent lavas from the Sunda arc range from those showing affinities with the island arc tholeiitic series, through a spectrum of calc-alkaline to high-K alkaline rocks. The tholeiitic rocks have relatively low 87Sr86Sr ratios averaging 0–7043; the calc-alkaline rocks show a wide range (from 0.7038 to 0.7059, averaging 0.7048); the high-K alkaline rocks average 0.7045. A rhyolitic ignimbrite from Sumatra has an 87Sr86Sr ratio of 0.7139.The relationship between 87Sr86Sr and major and trace element geochemistry is variable and complex. Lavas from the same volcano sometimes show significant differences in 87Sr86Sr despite close geochemical relationships. Rocks of the calc-alkaline suite show a regular decrease in 87Sr86Sr from West Java to Bali and there is some evidence for increasing 87Sr86Sr with increasing depth to the Benioff zone. Calc-alkaline and tholeiitic rocks from the Sunda arc have significantly higher 87Sr86Sr ratios than those from other island arcs, except from those arcs where continental crustal involvement has been inferred (e.g. New Zealand).A model of 87Sr enrichment due to isotopic equilibration of oceanic crust with sea water and disequilibrium melting in the slab and/or mantle is favoured to explain the Sr isotopic composition of the tholeiitic and normal calc-alkaline lavas. Calc-alkaline lavas with high 87Sr86Sr ratios are best explained by either sialic contamination, or the presence of alkali basalt as a component of the downgoing slab. The Sr isotopic data for the high-K alkaline lavas suggest a mantle origin. The high 87Sr86Sr ratio in the Lake Toba rhyolite implies a crustal origin.  相似文献   

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The isotopic composition of Sr has been measured in brine samples from the Upper Jurassic Smackover Formation in southern Arkansas; 87Sr86Sr ratios range from 0.7071 to 0.7101. With one exception, the 32 Smackover brines contain Sr which is significantly more radiogenic than the Sr in Late Jurassic sea water, indicating sizable Sr contributions from detrital sources. Isotopic analyses of core samples from rock units associated with the brines and regional stratigraphic relationships suggest that the radiogenic Sr was released from detrital minerals in Bossier shale to interstitial fluids expelled from the underlying Louann Salt in the North Louisiana salt basin. These fluids migrated through the Bossier Formation updip to the South Arkansas shelf, where they entered the upper Smackover carbonate grainstone. The radiogenic fluids mixed with Sr-rich interstitial marine waters that had the isotopic composition of Late Jurassic sea water; mixing in variable proportions resulted in the random distribution pattern of variable 87Sr86Sr ratios that is observed in Smackover brines within the 5000 km2 study area. Isotopic analyses of nonskeletal carbonate grains and coexisting coarse calcspar cement from the upper Smackover grainstone imply that the grains were diagenetically stabilized in the presence of interstitial marine waters, whereas the calcspar cement is a relatively late diagenetic phase precipitated after the arrival of radiogenic fluids.  相似文献   

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We have determined 87Sr86Sr ratios of the Tethys Sea by analyzing limestones of Permian to Late Cretaceous age from the overthrusted sequence of central and northern Euboea. The results are in satisfactory agreement with ratios obtained by other investigators on unreplaced fossil shells of similar age collected elsewhere. The 87Sr86Sr ratios of Mesozoic marbles from the autochtone metamorphic rocks of southern Euboea are more variable, perhaps because of increases in this ratio during regional metamorphism. Nevertheless, the lowest values of suites of isochronous samples may approach the correct ratio. Four samples of the Argyron Marble taken at different localities in southern Euboea and on the Attic peninsula have a concordant 87Sr86Sr ratio of 0.70688±0.00006 (1 \?gs), relative to 0.7080 for the Eimer and Amend isotope standard. This value indicates a Jurassic age for this formation even though the fragmentary fossil evidence favors a Late Cretaceous (Turonian) age.  相似文献   

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87Sr86Sr ratios have been determined in fifteen volcanic rocks from the northwestern part of the Hellenic arc. They range from 0.7041 to 0.7134. There is no apparent correlation of strontium isotope values with any major chemical component or with Rb/Sr ratios. The 87Sr86Sr ratios appear to increase in a general way with increasing depth to the Benioff zone. The strontium isotope ratios are higher than from most island arcs; this is believed to be due to contamination.  相似文献   

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Twelve samples of mid-Tertiary felsic volcanic rocks from Zacatecas and San Luis Potosí (both belonging to the Sierra Madre Occidental) and one sample of Lower Tertiary porphyritic andesite from Zacatecas are analyzed for 87Sr86Sr, K, Rb, and Sr. Eight selected samples are also analyzed for 143Nd144Nd. A linear regression of the present-day 87Sr86Srand87Rb86Sr of the felsic volcanic rocks in Zacatecas gives an approximate date of 30 ± 8 Ma. The initial 87Sr86Sr ratios are high and widely distributed (from 0.705 to 0.712 or higher) whereas the initial 143Nd144Nd ratios are somewhat low and show a narrow range (0.5125–0.5127). The available isotopic and trace-element data are best explained in terms of a binary mixing model in which the magmas derived from a slightly depleted-mantle fractionate and mix with varying proportions of the overlying middle/upper continental crust and undergo further shallow-level fractional crystallization before eruption. This model is also compatible with the trace-element and Sr isotopic data published from other areas of the Sierra Madre Occidental for which a purely mantle origin has been proposed.  相似文献   

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The isotopic composition of strontium of pore water and of authigenic minerals leached from the sediment of core 119K with hot aqua regia is similar to that of the brine in the Discovery deep and differs from that of normal seawater. The average 87Sr86Sr ratio of strontium removed by acid leaching is 0.7077 ± 0.0007 (1σ) compared to a value of 0.70904 for the Red Sea. The detrital silicate fraction exhibits an approximate inverse correlation between 87Sr86Sr ratios and strontium concentrations which provides tentative support for a model in which the detrital silicate fraction of deep-sea sediment is considered to be a mixture of terrigenous dust of sialic composition enriched in radiogenic 87Sr and of volcanogenic material of basaltic composition and low 87Sr abundance. The 87Sr86Sr ratios of the shells of foraminifers and pteropods, expressed as δ 87Sr‰ relative to 0.70904 for seawater, decrease from ?0.23 ± 0.17‰ at 90 cm to ?0.82 ± 0.17‰ at 273 cm and remain constant at this value to a depth of 450 cm. The lowering of the δ 87Sr values is attributed both to the presence of aragonite overgrowths on pteropod shells and to possible isotope exchange with strontium in the connate fluid.  相似文献   

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The 87Sr86Sr ratio in sea water has varied over geologic time due to the addition of strontium to the sea from rocks with a variety of 87Sr86Sr ratios. The measurements by Petermanet al. (Geochim. Cosmochim. Acta34, 105–120, 1970) of the value of the marine 87Sr86Sr ratio have been confirmed by several other workers and by some new measurements on JOIDES samples. They form the basis of a model calculation of the relative proportions of ‘basaltic’ (87Sr86Sr = 0.704) and ‘granitic’ (87Sr86Sr = 0.718) strontium being supplied to the sea. For the last 200 million years, the proportions of these two sources appear to reflect the history of global tectonics; ‘basaltic’ during rifting and increasingly ‘granitic’ during the present episodes of uplift and continental collision  相似文献   

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Strontium isotopic studies on twenty three whole rock kimberlites from two petrographic provinces in India show variation of initial 87Sr86Sr ratios from 0.7027 to 0.7102. The variation is unrelated to the degree of alteration. Between the micaceous and basaltic varieties there is some overlap in the Sr isotopic ratios. Leaching experiments on whole rock samples showed more highly radiogenic Sr in leaches compared to the bulk samples.In two diatremes, the initial 87Sr86Sr ratios show a positive correlation with RbSr which is believed to reflect a source event earlier than the formation of the kimberlites. The observed Sr isotopic data can be caused by (i) melting of a heterogeneous source or (ii) disequilibrium partial melting in the source region. In the former case, variable isotopic composition would be a necessary consequence of melting in small subsystems.  相似文献   

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Initial isotopic ratios of strontium have been determined in some calc-alkali rocks of Sardinia. The values of these ratios are from 0.7044 and 0.7047 in two basalts, and from 0.7063 to 0.7081 in five andesites. A dacite and a rhyolite have intermediate values of 0.7056 and 0.7058.It is suggested that increase of radiogenic strontium in andesite is most likely related to a contamination process involving water expelled from an underthrusting plate. This water also contributes to the increase in the potassium and related trace element contents in andesites.In spite of the87Sr86Sr difference between basalt and andesite, a cogenetic relationship between these two kinds of rocks cannot be precluded  相似文献   

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143Nd144Nd ratios measured in Quaternary lavas from Java and the Banda arc of Indonesia range from 0.51242 to 0.51280 and exhibit an inverse correlation with 87Sr86Sr. Isotopically, the Indonesian samples resemble Andean rather than island arc lavas. The samples from Java plot either within, or adjacent to the mantle array, towards higher 87Sr86Sr ratios. Samples from the Banda arc and the anomalous calc-alkaline volcano Papandajan are characterized by relatively low 143Nd144Nd and high 87Sr86Sr ratios. These characteristics are consistent with the interpretation that subducted terrigenous material was involved in the genesis of these lavas. Furthermore the Banda arc samples appear to lie on a mixing line between isotopic compositions characteristic of the mantle and upper continental crust. A high-K trachyte from the alkaline volcano Muriah, Java, has isotopic characteristics of the mantle (143Nd144Nd = 0.51270, 87Sr86Sr = 0.70424), which implies that the extreme enrichment in large-ion-lithophile elements in its source must have occurred only shortly before its formation. The inferred 143Nd144Nd ratio of the unmodified mantle beneath Java and the Banda arc is lower than that observed in mid-ocean ridge basalt, which may have important implications for a better understanding of the geochemical structure of the mantle.  相似文献   

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Morphological, mineralogical, chemical and RbSr isotopic studies have been made on Fesmectites (nontronites) from southern Pacific red clays cored near the Marquisas Islands. These minerals have at the top of the core, an 87Sr86Sr ratio of 0.70917 ± 0.00007, which indicates an authigenic origin in isotopic equilibrium with seawater. Weak leaching experiments with 1N HCl show that the nontronites also contain a volcanic component with a lower 87Sr86Sr ratio which, combined with the morphology of the particles, suggests a transportation by bottom currents of clay formed elsewhere.During burial, the nontronites experience diagenetic modifications resulting in an increase in Fe, K and Rb contents, a concomitant decrease of Mg, Ca, Ti, Na and Sr, and a preferential migration of radiogenic 87Sr from the clays into the surrounding pore waters.The 87Sr86Sr ratio of the Sr adsorbed on the outermost surfaces of the nontronites does not change with depth in the core, and is, therefore, independent of diagenetic influence, which is rather characterized by the 87Sr86Sr ratios of the interstitial waters. The isotopic composition of both the adsorbed Sr and that of the pore fluids may yield useful information on the crystallization environment and subsequent history of deep sea red clays.  相似文献   

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Strontium isotopic measurements were made on Late Proterozoic carbonates from West African Craton. Comparison of samples with acceptable trace element patterns with coeval data from southern Africa and with the published Australian results suggests that the 87Sr86Sr ratio of the Late Proterozoic sea water evolved in the following manner about 0.7075 at 1000 ± 50 Ma, 0.7056 to 0.7074 at 900 ± 50 Ma, 0.7068 to 0.7091(0.7106) at 800 ± 50 Ma, 0.7074 to 0.7077 at 700 ± 50 Ma, and 0.7076 to 0.7089(0.7096) at 600 ± 50 Ma ago. The variations are comparable in magnitude and frequency to those described previously for the Phanerozoic. Strontium isotopic values in the radiogenic part of this range suggest that the continental river flux of Sr into Late Proterozoic oceans was of comparable isotopic composition to its present day counterpart (~0.711). Consequently, the non-radiogenic 87Sr86Sr value at ~900 ± 50 Ma ago signifies a large flux of “mantle” strontium into the ocean at this time. Because the present time resolution is only about 75 ± 25Ma, additional sampling as well as better stratigraphie resolution and more definite selection criteria are required for construction of a more detailed Late Proterozoic sea water curve.  相似文献   

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Twenty-four groundwater samples from seven operating mines at Sudbury, Yellow-knife and Thompson (Ontario, North West Territories and Manitoba, resp.), all from depths greater than 1 km and ranging in total dissolved solids (TDS) from 1900 to 250,000 mg l?1, were measured for their 87Sr86Ar values. Each geographic location gives a limited range in values and each location is distinct from the others. This is interpreted as the result of extensive water-rock interaction on a local scale. For most of the time, these brines were isolated and only recently have been exposed to surface water as a result of the mining operations. The extent of the isolation is shown by the contrasting isotopic values of two “pockets” of water (0.711 vs. 0.716) located on opposite sides of the same fault system on the North Range at Sudbury. The exchange at all sites probably has continued until the present, as indicated by the close agreement between water and present-day87Sr86Sr whole-rock values. If so, it suggests that there is no single age for such brines, but it may be possible to date stages in the water's evolution by determining the age of secondary minerals that equilibrated with the water.  相似文献   

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