Trace element constraints on pegmatite genesis: Tin Mountain pegmatite,Black Hills,South Dakota     

Richard J. Walker  Gilbert N. Hanson  James J. Papike 《Contributions to Mineralogy and Petrology》1989,101(3):290-300

The Tin Mountain pegmatite is a small, zoned granitic body that is extremely enriched in Rb and Li, but has moderate concentrations of Sr and Ba. These trace elements are modelled using granitic distribution coefficients in order to test the potentials of partial melting of metasedimentary rocks and fractionation of a less-evolved granitic melt to have produced the parental liquid to the Tin Mountain pegmatite. Batch melting of any reasonable metasedimentary source rock would likely have yielded melts that were either insufficiently enriched in Rb and Li to be the parental liquid, or that had Sr and Ba concentrations that were much higher than those estimated for the parental liquid. The modelling of simple fractional crystallization and equilibrium crystallization of a granitic melt within the compositional range of the spatially associated Harney Peak Granite gives calculated melt compositions with either lower Sr and Ba concentrations or inadequate Rb and Li enrichments, to be the parent liquid of the pegmatite. At least two variants from simple crystal-liquid fractionation models can, however, successfully account for the derivation of the parent liquid: 1) generation of a Rb-, Li-, Ba- and Sr-rich granitic melt (outside of the compositional range of the sampled portions of the Harney Peak Granite complex) by low degrees of partial melting of metasedimentary rocks found in the Black Hills, followed by moderate extents of fractional or equilibrium crystallization, 2) derivation from Harney Peak granite via a complex, multi-stage crystal-liquid fractionation process, such as progressive equilibrium crystallization.  相似文献   

Rb-Sr provenance ages from weathered and stream transported quartz grains from the Harney Peak Granite,Black Hills,South Dakota     

Louise S. Powers  Hannes K. Brueckner  David H. Krinsley 《Geochimica et cosmochimica acta》1979,43(1):137-146

Weathered quartz grus and stream transported quartz of the Harney Peak Granite, Black Hills, South Dakota, contain low concentrations of Rb (generally 0.3–6.8 ppm) and Sr (0.2–2.0 ppm) and variable Sr isotopic ratios (0.759–1.070).Six of seven single grains of large composite quartz grus which recently entered the weathering environment define an apparent isochron age (about 1800 Myr) and initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio (0.7066) that approximate the whole-rock isochron age (1707 Myr) and initial ratio (0.7143) of the Harney Peak Granite. Apparently the Rb-Sr systematics of these grains were not significantly altered during initial weathering. Leached fluid inclusion material from a ca. 2 g aggregate of composite quartz grains contains very little Rb or Sr (0.019 and 0.17 μg, respectively) and has a very low ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio (0.739). The Rb and Sr content of the quartz grains appears to be concentrated in minute, heterogeneously-distributed mineral inclusions.Five aggregates of more completely weathered, small non-composite quartz grains produce a widely scattered pattern on an isochron diagram with all samples plotting below the 1707 Myr isochron. Examination by SEM of these grains shows solution and precipitation features on their relatively large effective surface areas. The differential precipitation of Rb is believed to have been the major perturbating chemical process during weathering.Three aggregates of stream quartz grains define an apparent isochron age of 1777 Myr and an initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio of 0.720 that suggest the initial ‘igneous’ Rb-Sr characteristics of the stream quartz were re-attained during their transportation, probably as a result of removal of the outer weathered surface by abrasion. The apparent resistance to chemical weathering of stream quartz and quartz which has just entered the weathering environment suggests that this mineral may be extremely useful in studies of provenance and the geochronology of strongly weathered terranes.  相似文献   

Graphic intergrowths of feldspars and quartz in some Czechoslovak pegmatites     

P. Černý 《Contributions to Mineralogy and Petrology》1971,30(4):343-355

Graphic intergrowths of alkali feldspar+quartz, and plagioclase+quartz, occur together in pegmatites in the eastern part of the Czechoslovak Moldanubicum. They form zones between the finer-grained wall zone and the central blocky feldspar+quartz core. The normative Or-Pig-Q compositions of the graphic intergrowths and the Or-Ab-An contents of their feldspars show broad variations generally, but have a restricted range within individual pegmatites. At two localities studied in more detail, coexisting feldspars show gradual changes in composition, from the margins up to the innermost graphic pegmatite, compatible with fractional crystallization along the feldspar solidus-solvus intersection in the Or-Ab-An-Q-H₂O system, at different vapour pressures in different pegmatites. Two models are demonstrated for low and high pressure cases. The feldspar compositions from central blocky zones deviate from the magmatic fractional crystallizations paths; this corresponds with the general assumption that they crystallized from supercritical gaseous fluids.In these and in similar pegmatites, coexisting alkali feldspar+quartz and plagioclase + quartz intergrowths are interpreted as the last products of cotectic crystallization from an ultimately fractionated granitic magma. Positive correlation of Ab solid solution and quartz content in the potassic intergrowths suggests that these characteristics may be indicative of the relative pressure and temperature effective during their crystallization, when compared in pegmatites of the same bulk composition.  相似文献   

Nd, O and Sr isotopic constraints on the origin of Precambrian rocks, Southern Black Hills, South Dakota     

Richard J. Walker  G. N. Hanson  J. J. Papike  J. R. O''Neil 《Geochimica et cosmochimica acta》1986,50(12):2833-2846

The Nd, O and Sr isotopic characteristics of Precambrian metasedimentary, metavolcanic and granitic rocks from the Black Hills of South Dakota are examined. Two late-Archean granites (2.5-2.6 Ga) have T_dm ages of 3.05 and 3.30 Ga, suggesting that at least one of the granites was derived through the melting of significantly older crust. Early-Proterozoic metasedimentary rocks have T_dm ages that range from 2.32 to 2.45 Ga. These model ages, in conjunction with probable stratigraphic ages ranging from 1.9 to 2.2 Ga, indicate that mantle-derived material was added to the continental crust of this region during the early-Proterozoic. Previous studies of the Harney Peak Granite complex have reported U-Pb and Rb-Sr ages of about 1.71 Ga and most granite samples examined in this study have Sr isotopic compositions consistent with that age. Two granite samples taken from the same sill, however, give two-point Rb-Sr and Sm-Nd ages of 2.08 ±0.08 and 2.20 ±0.20 Ga (∑²²⁰⁰_Nd = −15.5), respectively. In addition, whole-rock and apatite samples of the spatially associated Tin Mountain pegmatite give a Sm-Nd isochron age of 2000 ±100 Ma (∑²²⁰⁰_Nd = −5.8 ±1.8).

The Sm-Nd, O and Rb-Sr isotopic systematics of these granitic rocks have been complicated to some degree by both crystallization and post-crystallization processes, and the age of the pegmatite and parts of the Harney Peak Granite complex remain uncertain. Processes that probably complicated the isotopic systematics of these rocks include derivation from heterogeneous source material, assimilation, mixing of REE between granite and country rock during crystallization via a fluid phase and post-crystallization mobility of Sr. The Nd isotopic compositions of the pegmatite and the Harney Peak Granite indicate that they were not derived primarily from the exposed metasedimentary rocks.  相似文献   

Trace elements and Sr-isotopes in some mantle-derived hydrous minerals and their significance     

Asish R. Basu 《Geochimica et cosmochimica acta》1978,42(6):659-668

New analyses of K, Rb, Sr and Ba contents and the ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios of eight amphiboles, one phlogopite, two diopsides and one host alkalic basalt for an amphibole are reported: The samples are mostly inclusions in alkalic basalts and occur in association with peridotite inclusions. Two of the samples are from alpine-type peridotite bodies — one from the Etang de Lhers massif in the French Pyrenees and the other from the Finero massif in the Ivrea zone in northern Italy. The kaersutites come from the following localities: Hoover Dam, Arizona; Deadman Lake, California; Massif Central, France; Queensland; Spring Mountain, New South Wales.The data indicate that kaersutitic amphiboles are genetically unrelated to their host basalts. The isotopic and trace element data of these amphiboles further strengthens the suggestion of BASU and MURTHY (1977) that kaersutites play a significant role in ocean ridge basalt genesis. In addition, pargasitic amphibole with higher ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios, if present, may be important in the source regions of alkalic basalts.The bulk amphibole lherzolite from Lherz has the $\text{K}\text{Rb}$ratio and ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio appropriate for source material of ridge tholeiites. If the diopside and the amphibole in this rock had isotopically equilibrated under upper mantle conditions, the data show the time of last equilibration to be approximately 735 m.y., in contrast to the young emplacement age of the ultramafic massif.The coexisting phlogopite and diopside in the spinel lherzolite inclusion from Kilbourne Hole, New Mexico, show, surprisingly, isotopic equilibration under upper mantle conditions despite their drastically different $\text{Rb}\text{Sr}$ ratios. The data show that the phlogopite must have formed very recently in the upper mantle. This phlogopite also has a high $\text{K}\text{Rb}$ ratio (1133), contrary to the commonly held view that mantle phlogopites have low $\text{K}\text{Rb}$ ratios. The coexisting diopside shows high K content (778 ppm) and a lower $\text{K}\text{Rb}$ ratio than the phlogopite. This phlogopite lherzolite has trace elemental and isotopic characteristics that may be adequate for the origin of alkalic basalts upon partial melting.  相似文献   

Vredefort core: a cross-section of the upper crust?     

W.F Slawson 《Geochimica et cosmochimica acta》1976,40(1):117-121

Sixty-three samples from the granitic core of the Vredefort ring structure have been analyzed for K, Rb, and Sr. The $\text{Sr}{}^{87}\text{Sr}{}^{86}$ ratios were determined for thirteen of these. An isochron yielding an age of 2.85 × 10⁹ yr was obtained. The $\text{Rb}\text{Sr}$ and $\text{K}\text{Rb}$ ratios exhibit a ‘bulls-eye’ pattern in the granite suggesting the central portion has been extruded from depth. Diapiric flow and subsequent erosion has exposed a section of the continental crust within the Vredefort core.  相似文献   

纳米比亚湖山铀矿床中黑云母伟晶岩型矿石特征及铀矿化机制     

黄冉笑  袁国礼  王果胜  邱坤峰  邵华胜  龚能 《岩石学报》2021,37(5):1587-1610

湖山铀矿床位于纳米比亚达马拉造山带的南部中央带,属于伟晶岩型铀矿,是世界上最大的铀矿床之一。目前关于不同矿石中铀元素的富集与沉淀机制还存在一定争议。为了厘清岩浆演化过程与铀成矿作用的关系,本文对湖山铀矿床内E型伟晶岩型矿石开展了岩石学、矿物学和地球化学研究。野外调查及镜下鉴定结果表明,产铀的E型伟晶岩可以分为"简单类型"矿体和"复杂类型"矿体:前者具有花岗伟晶结构,工业铀矿物为晶质铀矿(含少量铀钍石),呈浸染状分布于石英、长石和黑云母之间,矿化程度低到中等;而后者表现出非均匀的结构特征,晶质铀矿在成因上与大量黑云母团块有空间联系,矿化程度极高。地球化学研究表明,在"简单类型"伟晶岩中,铀元素的富集受控于分离结晶作用,而在"复杂类型"伟晶岩中,铀矿化与同化混染作用密切相关。矿石的矿物-熔体相平衡模拟结果显示,外来基性组分(FeO、MgO、TiO_2)的混入导致"复杂类型"伟晶岩熔体中矿物的结晶顺序发生了改变,相比于"简单类型"伟晶岩熔体,黑云母初始结晶温度的升高和钾长石初始结晶温度的降低为黑云母提供了更充足的结晶时间和生长空间,促使黑云母以团块状聚集的形式产出。该过程会大量消耗岩浆中的F离子,引发UFm4-m络合物的水解,促使晶质铀矿在团块黑云母的附近沉淀,形成高品位的铀矿化。因此,本文有关"简单类型"和"复杂类型"伟晶岩矿石的研究,有效地揭示了矿化过程,丰富了伟晶岩型铀矿床理论,为推动铀矿勘查与开发提供了科学依据。  相似文献   

Petrologic and geochemical links between the post-collisional Proterozoic Harney Peak leucogranite, South Dakota, USA, and its source rocks   总被引：6，自引：0，他引：6  

Peter I. Nabelek  Cindy D. Bartlett 《Lithos》1998,45(1-4):71-85

The Proterozoic terrane of the Black Hills, South Dakota, includes the composite Harney Peak leucogranite and associated pegmatites that were emplaced into metamorphosed pelites and graywackes. Available dates indicate that granite generation post-dated regional metamorphism and deformation that have been attributed to collision of the Wyoming and Superior cratons at 1760 Ma. Previous radiogenic and stable isotope work indicates that the exposed metasedimentary rocks are equivalent to sources of the leucogranites. In this study, whole rock and mineral compositions of the metasedimentary rocks were used to calculate the likely average residue mineralogies and melt fractions that would be generated by muscovite dehydration melting of the rocks. These were then used to model observed trace element compositions of the granites using published mineral/melt distribution coefficients. Model trace element melt compositions using pelitic and graywacke protoliths yield similar results.

The models reproduce well the observed depletion of transition metals and Ba in the granites relative to metasedimentary protoliths. The depletion is due mainly to high proportion of biotite with variable amounts of K-feldspar in the model residue. Sr is also depleted in the granites compared to source rocks, but to a lesser relative extent than Ba. This is because of the low biotite/melt distribution coefficient for Sr and because high proportion of plagioclase in the residue is compensated by high Sr concentrations in protoliths. Rubidium, Cs and Ta behaved as slightly compatible to incompatible elements, and therefore, were not strongly fractionated during melting. Of the considered elements, only B appears to have been highly incompatible relative to residue during melting. The protoliths had sufficient B to allow tourmaline crystallization in those parts of the Harney Peak Granite in which Ti concentration was sufficiently low not to enhance crystallization of biotite.

The reproducibility of observed trace element concentrations in the Harney Peak Granite by the models supports the often made proposition that metapelites and metagraywackes are common sources for leucogranites. This argues against mass input from the mantle into metagraywacke and metapelitic crustal sources or melting of amphibolites to generate the post-collisional Harney Peak and other similar peraluminous granite suites.  相似文献   

RbSr studies of CI and CM chondrites     

David W Mittlefehldt  George W Wetherill 《Geochimica et cosmochimica acta》1979,43(2):201-206

RbSr whole rock analyses have been performed on 2 CI and 3 CM chondrites. Four of these stones (Ivuna, Orgueil, Cold Bokkeveld and Erakot) were previously studied in this laboratory and were shown to be discordant from a 4.6 Gyr isochron. The fifth, Murchison, was not previously studied. The new data support the discordance of the first four stones, and indicate that Murchison is also discordant. Studies of Sr isotope ratios in unspiked Orgueil show that the discordance is not due to inhomogeneities in the $\text{Sr}{}^{84}\text{Sr}{}^{86}$ ratio caused by incomplete mixing of nucleosynthesis products.In order to gauge the effects of weathering, two leaching experiments were performed on fresh, interior samples of Murchison; one for a period of 1.5 hr and the other for 117 hr. The results indicate that the relative solubility of nonradiogenic Sr is approximately twice that of Rb and radiogenic Sr is more soluble than the nonradiogenic Sr. This gives the residue a lower model age than the whole rock both by increasing the $\text{Rb}\text{Sr}$ ratio and by decreasing the $\text{Sr}{}^{87}\text{Sr}{}^{86}$ ratio. This result is in contrast to that expected from studies of ordinary chondrite finds, which generally show higher model ages than falls. The constancy of $\text{K}\text{Rb}$ and $\text{K}\text{Sr}$ ratios between the two leaching experiments, and their difference from the unaltered whole rock ratios suggest that the bulk ratios are produced by dissolution of a single phase, and the higher radiogenic Sr content by selective leaching of other phases.  相似文献   

The rare alkalies in hydrothermal alteration at Wairakei and Broadlands,geothermal fields,N.Z.     

Reiner Goguel 《Geochimica et cosmochimica acta》1983,47(3):429-437

Drillcores and waters from Wairakei and Broadlands geothermal areas New Zealand have been analyzed for Li, Rb, Cs, Na, K, Mg, Ca, Al, Ti, Mn, and Be. The drillcores were altered to various degrees at temperatures below 300°C in slightly alkaline chloride water, probably derived from rock-water interaction in untapped horizons at higher temperature. It changes its composition as it leaches Ca and Na from the rock and adds K, Rb, Cs and Li. Evaluation of these changes in relation to the dimensions of the altered zone under observation suggests that a high mass ratio of water to rock (e.g., 100) and a period of up to 1 million years are responsible for the present stage of alteration.Increase of K and Rb in the altered rocks is a result of the formation of abundant adularia in addition to illite. The $\text{K}\text{Rb}$ ratio of the rock decreases during alteration but remains higher than that of the fluid. Only clay materials and zeolites that preferentially absorb Rb give slightly lower $\text{K}\text{Rb}$ ratios than the fluid.The mineral phases responsible for the uptake of lithium during alteration are chlorite (300 ppm Li) and quartz (up to 430 ppm Li). Li uptake in quartz is considered to be the mechanism by which Al-rich quartz crystallises from alumino-silicates. $\text{Li}\text{Al}$ atomic ratios of 0.3–0.57 and Al concentrations up to 3000 ppm have been observed.Relatively small concentrations of Cs are found in potassic minerals (e.g. 10 ppm Cs in adularia, 44 ppm Cs in illite). However, 240 ppm Cs are found in wairakite from Wairakei equilibrated at 235°C. Lower equilibration temperatures may lead to higher cesium concentrations. This effect, in conjunction with a more concentrated hydrothermal fluid, could explain a content of 4500 ppm Cs in wairakite extracted from a drillcore taken in the El-Tatio geothermal field in Chile.  相似文献   

Luminescence of Eu<Superscript>2+</Superscript> in feldspars from muscovite pegmatites     

L. N. Sapozhnikova  V. V. Moroshkin  I. A. Zhukova 《Geology of Ore Deposits》2007,49(7):565-572

The data on photoluminescence (PL) that precisely detects Eu²⁺ centers and X-ray luminescence (XL) were compared for plagioclases and potassium feldspars in 21 samples from muscovite pegmatites of the Mama region. The Eu contents determined in 10 samples vary from 10^?4 to 10^?6 wt %. Europium occurs mainly as bivalent species that replaces Sr²⁺, Ca²⁺, and Ba²⁺. Eu is gained in the products of early crystallization, and its relative amounts decrease by an order of magnitude in the course of pegmatite formation down to complete disappearance in late generations of feldspars. It is shown that Eu²⁺ can be detected in XL spectra, and the Eu²⁺ content can be determined in qualitative terms, for instance, by the intensity of radiation band 400–420 nm in plagioclase.  相似文献   

KRb ratios in some volcanic rocks from Mauritius,Indian Ocean     

A.N Baxter 《Geochimica et cosmochimica acta》1975,39(11):1573-1576

$\text{K}\text{Rb}$ ratios in Mauritian Older Series basalts range from 200 to 350. A fall to around 175 in trachytes probably relates to kaersutite fractionation. Highly variable ratios in Intermediate  相似文献   

Theoretical studies of the alteration of spodumene,petalite, eucryptite and pollucite in granitic pegmatites: exchange reactions with alkali feldspars     

Scott A. Wood  Anthony E. Williams-Jones 《Contributions to Mineralogy and Petrology》1993,114(2):255-263

The ratios Na/Li, K/Li, Na/Cs and K/Cs have been calculated for exchange equilibria among the Li and Cs silicates spodumene, petalite, eucryptite, and pollucite, and the alkali feldspars albite and K-feldspar plus quartz, in pure water and in chloride solutions at temperatures from 100° to 700°C and pressures from 0.5 to 4 kbar, using available thermodynamic data for minerals and the modified HKF equation of state for aqueous species. For exchange equilibria between Li-bearing aluminosilicates and the alkali feldspars, the activities of the alkali metals in solution under most of the conditions investigated follow the order Li>Na>K, and Na/Li and K/Li decrease with decreasing temperature. For exchange equilibria between pollucite and the alkali feldspars the order is Na>K>Cs in solution; Na/Cs and K/Cs increase strongly with decreasing temperature. The absolute values of these alkali metal ratios are in good agreement with the few available experimental data. The effect of chloride ion pairing on the calculated ratios is slight and does not consistently improve agreement between theory and experiment. These results suggest that the alteration of eucryptite, petalite or spodumene to albite and/or K-feldspar should be a normal consequence of the closed system evolution of rare element pegmatites upon cooling, in agreement with the ubiquity of such phenomena world-wide. On the other hand, alteration of pollucite to albite or K-feldspar upon cooling is only likely to occur if external fluids, with very high Na/Cs and/or K/Cs ratios, gain access to the pegmatite. Owing to the heterogeneity of rare element pegmatites, the fluid need not be external to the entire pegmatite, but could be simply external to the particular zone containing pollucite. Fluids in equilibrium with typical subsolidus rare metal pegmatite assemblages will invariably have high Li contents, thus explaining the common occurrence of Li-metasomatic halos about pegmatites. These same fluids are predicted to have relatively low Cs contents, in apparent agreement with the lesser role of Cs relative to Li in metasomatic halos. However, preferential formation of complexes of the alkali metals with fluoride, borate or aluminosilicate components potentially could alter the calculated alkali metal behaviors.  相似文献   

Kiglapait geochemistry V: Strontium     

S.A Morse 《Geochimica et cosmochimica acta》1982,46(2):223-234

The Kiglapait intrusion contains 330 ppm Sr and has $\text{Sr}\text{Ca}\text{= 5 × 10}{}^{\mathrm{?3}}$ and $\text{Rb}\text{Sr}\text{= 3 × 10}{}^{\mathrm{?3}}$, as determined by summation over the Layered Group of the intrusion. Wholerocks in the Lower Zone contain 403 F_L^0.141 ppm Sr, where F_L is the fraction of liquid remaining; Sr drops to 180 ppm at the peak of augite production (F_L = 0.11) and rises to a maximum of 430 ppm in the Upper Zone before decreasing to 172 ppm at the end of crystallization. Feldspars in the Lower Zone contain 532 F_L^0.090 ppm Sr, increasing to 680 ppm in the Upper Zone before decreasing to 310 ppm at the end. Clinopyroxenes contain 15 to 30 ppm Sr and have a mineral-melt distribution coefficient D = 0.06 except near the top of the intrusion where D = 0.10.The calculated feldspar-liquid distribution coefficient has an average value near 1.75 but shows four distinct trends when plotted against X_An of feldspar. The first two of these are strongly correlated with the modal augite content of the liquid, on average by the relation D = 1.4 + 0.02 Aug^L. The third (decreasing) trend is due to co-crystallization of apatite, and the fourth (increasing) trend can best be attributed to a triclinic-monoclinic symmetry change in the feldspar at An₂₆, 1030°C. The compound feldspar-liquid distribution coefficient K_D for $\text{Sr}\text{Ca}$ bears out these deductions in detail and yields ΔG_r for the Sr-Ca exchange ranging from nearly zero at the base of the Lower Zone to ?26 kJ/gramatom at the end of crystallization. The compound feldspar-liquid distribution coefficient K_D for $\text{Rb}\text{Sr}$ varies from 0.3 in the Lower Zone to 1.1 at the end of crystallization.The ratio $\text{Ca}{}^{\mathrm{F}}\text{Ca}{}^{\mathrm{L}}$ is about 1.45 for troctolitic liquids containing 5% augite, for which K_D (Sr-Ca) = 1.0 and D_Ca = D_Sr. For common basaltic liquids containing 20% augite, the Kiglapait data predict $\text{solSr}{}^{\mathrm{F}}\text{Sr}{}^{\mathrm{L}}\text{= 1.8}$, as commonly found elsewhere. The strong dependence of D_sr on augite content of the liquid illuminates the role of liquid composition and structure in determining the feldspar-liquid distribution coefficient. Conversely, a discontinuous change in the trend of D_Sr when apatite arrives shows that the effect is due to apatite crystallization itself, not to the continuous variation of the liquid as it becomes enriched in apatite component.  相似文献   

Sr and Nd isotopic evidence for petrogenesis of mid-tertiary felsic volcanism in the mineral district of Zacatecas,Zac. (Sierra Madre Occidental), Mexico     

Surendra P. Verma 《Chemical Geology》1984,46(1):37-53

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 ${}^{87}\text{Sr}{}^{86}\text{Sr}$, K, Rb, and Sr. Eight selected samples are also analyzed for ${}^{143}\text{Nd}{}^{144}\text{Nd}$. A linear regression of the present-day ${}^{87}\text{Sr}{}^{86}\text{Sr}\text{and}{}^{87}\text{Rb}{}^{86}\text{Sr}$ of the felsic volcanic rocks in Zacatecas gives an approximate date of 30 ± 8 Ma. The initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios are high and widely distributed (from 0.705 to 0.712 or higher) whereas the initial ${}^{143}\text{Nd}{}^{144}\text{Nd}$ 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   

$\text{K}\text{Rb}$ ratios in Precambrian granulite terranes     

Jerry D. Lewis  Charles M. Spooner 《Geochimica et cosmochimica acta》1973,37(5):1111-1118

Concentrations of potassium and rubidium are reported for 62 Precambrian shield whole-rock samples belonging to the pyroxene granulite facies of world-wide distribution. Compared with the Main Trend established by Shaw (1968) for igneous and quasi-igneous rocks of the upper crust, the high-grade metamorphic granulites exhibit a similar correlation but with a measurable depletion in Rb for a given K content. The Metamorphic Trend may be described by the equations: log₁₀ (ppm Rb) = 1.136 log₁₀ (per cent K) + 1.495 or ppm Rb = 31.28 (per cent K)^1.136. The square of the product moment correlation coefficient shows that 80 per cent of the variation in Rb is associated with variation in K.All suites studied have initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratios less than 0.707. This low value argues against repeated extraction of Rb and K through time on a regional scale. Rather, the major depletion in these lithophile elements occurred in the early stages of crustal evolution.  相似文献   

Geochemistry and petrology of dredged basalts from the Bouvet triple junction,South Atlantic     

John S. Dickey  Frederick A. Frey  Stanley R. Hart  E.Bruce Watson  Geoffrey Thompson 《Geochimica et cosmochimica acta》1977,41(8):1105-1118

Basalts dredged from the Bouvet triple junction (South Atlantic), from the Mid-Atlantic Ridge near the triple junction, and from a spreading center east of Bouvet Island differ from normal mid-ocean ridge tholeiites by having higher concentrations of K and other large-ion-lithophile elements, higher ${}^{87}\text{Sr}\text{:}{}^{86}\text{Sr}$ ratios, and rare earth element distributions which show relative enrichment in the lighter rare earths. The basalts are more fractionated than typical oceanic tholeiites, however, fractional crystallization does not fully account for their chemical characteristics, and it appears that they were derived from special source materials, contaminated perhaps by a mantle plume rising beneath Bouvet Island.  相似文献   

⁸⁷Rb-⁸⁷Sr age of fragments and soils from the lunar sea of fertility     

Jean Louis Birck  Claude J Allegre 《Geochimica et cosmochimica acta》1973,37(9):2025-2031

The Luna 16 materials were dated by the Rb-Sr method.An internal isochron age of 3.4 ± 0.2 has been determined for a 6 mg fragment.The Luna 16 total soil is poorer in radiogenic Sr than any other analyzed soil from the Moon. Apollo 14 and 15 soils have also been studied; all of them fall nearly on a 4.65 b.y. isochron with the ADOR initial ${}^{87}\text{Sr}{}^{86}\text{Sr}$ ratio.A comparison of the integrated $\text{Rb}\text{Sr}$ of the basalt source region and the $\text{Rb}\text{Sr}$ of the rocks suggests that these basaltic fragments have been generated with only minor $\text{Rb}\text{Sr}$ fractionation.The existence of an old Rb-rich subcrust which contaminated the basalts is also in agreement with the present results.  相似文献   

阿尔泰可可托海3号脉伟晶岩型稀有金属矿床云母和长石的矿物学研究及意义   总被引：8，自引：4，他引：4  

周起凤  秦克章  唐冬梅  丁建刚  郭正林 《岩石学报》2013,29(9):3004-3022

可可托海3号脉伟晶岩型稀有金属矿床是阿尔泰造山带产出的规模最大的伟晶岩脉,其完美的同心环状结构分带举世闻名。云母和长石作为3号脉9个结构带的贯通性矿物,由外向内表现不同的结构和成分特征。其中,云母由白云母系列向锂云母系列演化,白云母呈黄-绿色中细粒→白色或绿色中粗粒-巨晶→白色或绿色书状集合体→白色或绿色中粗粒-巨晶,锂云母呈玫瑰紫中细粒鳞片状或楔状集合体,BSE图像下云母表现出成分分带及不平衡和交代结构;长石主要为钾长石和钠长石,及少量斜长石,钾长石主要呈块体产出,钠长石呈细粒→叶片状→薄片状产出。本次研究通过电子探针(EMPA)和激光剥蚀等离子质谱(LA-ICP-MS)获得3号脉各结构带云母和长石的主微量成分。3号脉云母具有高Li(249×10^-6~35932×10^-6)、Rb(1240×10^-6~22825×10^-6)、Cs(35.9×10^-6~13980×10^-6)、Ta(13.3×10^-6~447×10^-6)含量、低K/Rb值(4.23~59.4)和K/Cs值(6.53~2368),钾长石具有低K/Rb值(35.4~1865),且由外向内,随K/Rb值降低,云母的Li、Rb、Cs、F、Ta含量升高,表明3号脉是一个由外向内结晶的分异演化程度较高的伟晶岩脉。另外,连续相邻结构带中云母和长石的主微量成分呈振荡变化,该现象主要受熔体不混溶过程的控制,也受矿物结晶不平衡影响,而熔体不混溶过程也是控制3号脉结构分带的机制之一。外部带(I-IV带)和内部带(V-VIII带)的云母和碱性长石在成分(FeO、Li、Rb、Cs、F、Ta含量和K/Rb值及K/Cs值)和结构(不平衡和交代结构)上具有明显差异,内部带演化程度明显加大,流体组分比例升高,表明体系由以熔体为主的阶段(外部带)进入以熔流体为主相对不稳定的阶段(外部带)。结合野外观察的证据,促使体系在IV带和V带间发生突然转变而进入熔流体阶段的是一个泄压事件。  相似文献   

陕南光石沟伟晶岩型铀矿床中长石矿物化学初步研究   总被引：1，自引：0，他引：1  

冯张生 《化工矿产地质》2012,34(2):71-76

以光石沟伟晶岩型铀矿床中相关伟晶岩中的长石为研究对象,开展系统的矿物化学电子探针研究,结果显示其中的斜长石都属于更长石、钠长石,碱性长石均为透长石,运用二长石温度计计算出了四种类型伟晶岩的结晶温度。通过研究,认为4种类型伟晶岩具有岩浆演化关系,从不含矿黑云母伟晶岩-含矿黑云母伟晶岩-二云母伟晶岩-白云母伟晶岩,随着伟晶岩岩浆演化程度的增高,成岩结晶温度不断降低,岩浆逐渐向酸性演化,同时由于黑云母等富氟矿物的产出,导致晶质铀矿的沉淀而富集成矿。  相似文献