首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献，搜索用时 31 毫秒
1.
This study presents Sr and Pb isotopic ratios and Rb, Sr, U, Th, and Pb concentrations of an ultrapotassic basaltic suite and related rocks from the central Sierra Nevada, California. The ultrapotassic suite yields a narrow range of Sr and Pb isotopic compositions (87Sr/86Sr=0.70597–0.70653; 206Pb/ 204Pb=18.862–19.018; 207Pb/204Pb=15.640–15.686; 208Pb/ 204Pb=38.833–38.950). Associated basalts containing ultramafic nodules have less radiogenic Sr (87Sr/86=0.70430–0.70521) and generally higher Rb/Sr ratios than the ultrapotassic suite. Leucitites from Deep Springs Valley, California, contain high 87Sr/86Sr (71141–0.71240) and low 206Pb/204Pb (17.169–17.234) ratios, reflecting contamination by crustal granulite.The isotopic relationships support an origin of the ultrapotassic basaltic suite by partial melting of an enriched upper mantle source. Dehydration of a gently inclined oceanic slab beneath the Sierra Nevada may have provided Ba, K, Rb, Sr, and H2O, which migrated into the overlying upper mantle lithosphere. The end of subduction 10 m.y. ago allowed increased asthenospheric heat flow into the upper mantle lithosphere. The increased heat flow enhanced fluid movement in the upper mantle and contributed towards isotopic homogenization of the upper mantle source areas. Continued heating of the enriched upper mantle caused partial melting and subsequent eruption of the ultrapotassic lavas.  相似文献   

2.
We analyzed 17 fragments from a zoned allanite–epidote crystal (ca 2.2 mm × 4.0 mm), which had formed during different prograde and retrograde stages of ultra high pressure (UHP) and amphibolite facies metamorphism (240–230 Ma, Sulu Belt, E China), for the isotopic composition of Pb, Nd, and Sr and contents of Pb, U, and Th, Sr and Rb, and Nd and Sm. Since most fragments had 238U/204Pb and 232Th/204Pb values less than 1, corrections for in situ Pb growth are small and uncertainties in the recalculation of the Pb isotopic compositions to 240 Ma are insignificant. The recalculated Pb falls on a linear trend in the 206Pb/204Pb vs 207Pb/204Pb diagram with the allanite defining the low–206Pb/204Pb end (17.07) of this trend and the epidote defining its high–206Pb/204Pb end (17.56). The recalculated data scatter in the 206Pb/204Pb vs 208Pb/204Pb diagram, which implies that the initial Pb isotopic variation reflects the involvement of at least three different Pb sources. The low 87Rb/86Sr values account for a change in 87Sr/86Sr by in situ 87Sr growth of less than 0.0007, which implies that the isotopic heterogeneity of 87Sr/86Sr (0.70601–0.7200) is a primary feature. The Pb and Sr isotope data unequivocally demonstrate that contributions from different precursor minerals result in initial isotopic heterogeneity in the metamorphic reaction product. It is likely that such an initial isotopic heterogeneity also exists for Nd, but it could not be resolved in the present study. Initially heterogeneous Pb and Sr isotope compositions imply that age differences between core and rim of large crystals may result in the determination of highly arbitrary geological rates, especially for minerals with relatively low parent-to-daughter ratios.  相似文献   

3.
Inductively coupled plasma mass spectrometry (ICP-MS) has been used to measure the concentration and isotopic composition of Pb in archaeological human and animal skeletal remains, soil from a village site of the Omaha tribe (U.S.A.) and cosmetic pigments.Lead concentrations in human bones from the Omaha tribe vary between 4.8 and 2570 μg/g, with younger people having the highest concentrations. Lead concentrations in animal bones from an Omaha village vary between 0.6 and 3.7 μg/g, and those of three soil samples range between 18 and 21 μg/g. Lead concentrations found in human bones from Anasazi (Utah, U.S.A.) and Alta (Peru) populations vary between 0.7 and 3.2 μg/g.Isotope ratios of a reagent grade Pb(NO3)2 solutions were measured by thermal ionization mass spectrometry (TIMS), as well as by ICP-MS to provide laboratory reference materials. The accuracy of the ICP-MS measurements relative to TIMS for the standard solution were found to be within 0.02–0.31% for206Pb/204Pb, 0.02–0.55% for207Pb/204Pb, and 0.16–0.56% for208Pb/204Pb. The precision of measurements on artifacts was 0.42–0.65% for206Pb/204Pb and 0.41–0.62% for207Pb/204Pb, whereas the precision for the same ratios for the bones was 0.85–1.8 and 0.82–1.67%, respectively. For the cosmetic lead-bearing pigments, a precision of 0.07–0.15% was found for both206Pb/204Pb and207Pb/204Pb ratios. Lead isotope ratios of artifacts give a radiogenic Pb signature, of which are close to signatures from PbZn mines of the central U.S. region. Lead isotope ratios of the pigments give non-radiogenic Pb signatures. Lead isotope ratios of the bones differ from those of the artifacts, and although similar in isotopic ratio to the pigments, they are more scattered, suggesting potential mixing of Pb from different regions.  相似文献   

4.
U–Pb isotopic analyses indicate that ores from the South Zhuguang uranium ore field, south China, have high common (non‐radiogenic) Pb contents, with variable and relatively radiogenic initial Pb contents. The U–Pb isochron method was used to date these ores, with plots of 208Pb/204Pb and 207Pb/204Pb versus 206Pb/204Pb being used to identify sample suites with similar initial Pb isotopic ratios and to normalize variable initial Pb isotopic ratios. The resulting U–Pb isochrons indicate two substages of uranium mineralization at ~57 and 52 Ma, with a later hydrothermal reformation at ~49 Ma, which homogenized Pb isotopic compositions. Initial Pb isotopic systematics indicate that the ore‐forming fluid was characterized by high 206Pb/204Pb and 207Pb/204Pb ratios and low 208Pb/204Pb ratios, suggesting that the ore‐forming fluid was sourced from Cretaceous–Paleogene red‐bed basins, rather than from magma or the mantle, with consideration of mineralization ages.  相似文献   

5.
Lead isotope ratios of galena from the carbonate-hosted massive sulphide deposits of Kabwe (Pb-Zn) and Tsumeb (Pb-Zn-Cu) in Zambia and Namibia, respectively, have been measured and found to be homogeneous and characteristic of upper crustal source rocks. Kabwe galena has average isotope ratios of 206/204Pb = 17.997 ± 0.007, 207/204Pb = 15.713 ± 0.010 and 208/204Pb = 38.410 ± 0.033. Tsumeb galena has slightly higher 206/204Pb (18.112 ± 0.035) and slightly lower 207/204Pb (15.674 ± 0.016) and 208/204Pb (38.276 ± 0.073) ratios than Kabwe galena. The isotopic differences are attributed to local differences in the age and composition of the respective source rocks for Kabwe and Tsumeb. The homogeneity of the ore lead in the two epigenetic deposits suggests lead sources of uniform isotopic composition or, alternatively, thorough mixing of lead derived from sources with relatively similar isotopic compositions. Both deposits have relatively high 238U/204Pb ratios of 10.31 and 10.09 for Kabwe and Tsumeb galenas, respectively. These isotope ratios are considered to be typical of the upper continental crust in the Damaran-Lufilian orogenic belt, as also indicated by basement rocks and Cu-Co sulphides in stratiform Katangan metasediments which have a mean μ-value of 10.25 ± 0.12 in the Copperbelt region of Zambia and the Democratic Republic of Congo (formerly Zaire). The 232Th/204Pb isotope ratios of 43.08 and 40.42 for Kabwe and Tsumeb suggest Th-enriched source regions with 232Th/235U (κ-values) of 4.18 and 4.01, respectively. Model isotopic ages determined for the Kabwe (680 Ma) and Tsumeb (530 Ma) deposits indicate that the timing of the mineralisation was probably related to phases of orogenic activity associated with the Pan-African Lufilian and Damaran orogenies, respectively. Galena from the carbonate-hosted Kipushi Cu-Pb-Zn massive sulphide deposit in the Congo also has homogeneous lead isotope ratios, but its isotopic composition is comparable to that of the average global lead evolution curve for conformable massive sulphide deposits. The μ (9.84) and κ (3.69) values indicate a significant mantle component, and the isotopic age of the Kipushi deposit (456 Ma) suggests that the emplacement of the mineralisation was related to a post-tectonic phase of igneous activity in the Lufilian belt. The isotope ratios (206/204Pb, 207/204Pb, 208/204Pb) of the three deposits are markedly different from the heterogeneous lead ratios of the Katangan Cu-Co stratiform mineralisation of the Copperbelt as well as those of the volcanogenic Nampundwe massive pyrite deposit in the Zambezi belt which typically define radiogenic linear trends on lead-lead plots. The host-rock dolomite of the Kabwe deposit also has homogeneous lead isotope ratios identical to the ore galena. This observation indicates contamination of the Kabwe Dolomite Formation with ore lead during mineralisation. Received: 8 September 1997 / Accepted: 21 August 1998  相似文献   

6.
The paper considers the results of high-precision Pb–Pb isotopic analysis of 120 galena samples from 27 Au and Ag deposits of the South Verkhoyansk Synclinorium (SVS) including large Nezhdaninsky deposit (628.8 t Au). The Pb isotopic composition is analyzed on a MC-ICP-MS NEPTUNE mass-spectrometer from solutions with an error of no more than ±0.02% (2σ). Four types of deposits are studied: (i) stratified vein gold–quartz deposits (type 1) hosted in metamorphosed Upper Carboniferous–Lower Permian terrigenous rocks and formed during accretion of the Okhotsk Block to the North Asian Craton synchronously with dislocation metamorphism and related granitic magmatism; (ii) vein gold–quartz (Nezhdaninsky type) deposits also hosted in Lower Permian metasedimentary rocks; (iii) Au–Bi deposits localized at the contact zones of the Late Cretaceous granitic plutons; and (iv) Sn–Ag polymetallic deposits related to granitic and subvolcanic rocks of the Okhotsk Zone of the SVS. The deposits of types 2, 3, and 4 are postaccretionary. The general range of 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios is 18.1516–18.5903 (2.4%), 15.5175–15.6155 (0.63%), and 38.3010–39.0481 (2.0%), respectively. In 206Pb/204Pb–207Pb/204Pb and 206Pb/204Pb–208Pb/204Pb diagrams, the data points of Pb isotopic compositions of all deposits occupy restricted, partly overlapping areas along a general elongated trend. The various SVS Au–Ag deposits can be classified according to the Pb isotopic composition in accordance with all three Pb ratios. Deposits of the same type show distinct Pb isotopic compositions that strongly exceed the scale of analytical error (±0.02%). The differences in Pb isotopic composition within specific deposits are low and subordinate and have little effect on variations in the Pb isotopic composition of the SVS deposits. The μ2 values (Stacey–Kramers model), which characterize the 238U/204Pb ratios of ore lead sources of the SVS deposits, widely vary from 9.7 to 9.38. The ω2 values (232Th/204Pb) are 39.82–36.61, whereas the Th/U ratios are 4.04–3.86. The content of all three radiogenic Pb isotopes and μ2 values of feldspars from SVS intrusive rocks are strongly distinct from those of galena of stratified gold–quartz and vein gold–quartz deposits and are identical to Pb of galena from Au–Bi and Sn–Ag polymetallic deposits, indicating a mostly magmatic origin for the Pb of these deposits. Detailed isotopic study of the Nezhdaninsky deposit shows different Pb isotopic composition of two consecutive mineral assemblages (gold–sulfide and Ag polymetallic): ~0.30, ~0.07, and ~0.22% for 206Pb/204Pb, 207Pb/204Pb, and 208Pb/204Pb ratios, respectively. These differences are interpreted as a result of involvement of at least two metal sources during the evolution of an ore-forming system: (i) host Lower Permian terrigenous rocks and (ii) a magmatic source similar in Pb isotopic composition to that of Sn–Ag polymetallic deposits. The Pb isotopic composition and μ2 and Th/U values show that lead of stratified gold–quartz deposits combines isotopic tracers of lower and upper crustal sources (Upper Carboniferous–Lower Permian terrigenous rocks), lead of which was mobilized by ore-bearing fluids. The high 208Pb/206Pb ratios and Th/U evolutionary parameter are common to all Pb isotopic composition of all studied Au–Ag deposits and SVS Cretaceous intrusive rocks and indicate that Pb sources were depleted in U relative to Th. Taking into account the structure of the region and conceptions on its evolution, we can suggest that the magma source was related to lower crustal subducted rocks of the Archean (~2.6 Ga) North Asian Craton and the Okhotsk terrane.  相似文献   

7.
The Neoproterozoic Vazante Group at the western border of the São Francisco Craton, Brazil, hosts the largest Zn–Pb district in South America. Several authors have classified this mineral district as Mississippi Valley-type (MVT), based on the intimate association with carbonates and the epigenetic character of most ore bodies. In this paper, we present 47 new lead isotope data from four deposits located along the 300 km N–S Vazante–Paracatu–Unai linear trend. Pb isotope ratios indicate sources with relatively high U/Pb and Th/Pb ratios. Considering the 206Pb/204Pb and 208Pb/204Pb ratios as indicative parameters for the source, we suggest an upper crustal source for the metals. The small variation on the Pb isotope ratios compared to those observed in the classical MVT deposits, and other geological, fluid inclusion and sulphur isotopic data indicates a metallogenic event of long duration. It was characterized by focused circulation of hydrothermal fluids carrying metals from the basement rocks and from the sedimentary pile. The data obtained are more compatible with an evolution model similar to that of IRISH-type deposits. The existence of three Pb isotopic populations could be the result of regional differences in composition of the source rocks and in the fluid–rock interaction since the mineralization is a long-term process.  相似文献   

8.
The isotopic (U-Pb, 238U-235U, 234U-238U) and chemical study of whole-rock samples and finegrained fractions of rocks in a vertical section of the terrigenous sequence at the Dybryn uranium deposit in the Khiagda ore field shows that a wide U-Pb isotopic age range (26.9-6.5 Ma) is caused by oxidation and disturbance of the U-Pb isotopic system in combination with protracted uranium ore deposition. The oxidation of rocks resulted in the loss of uranium relative to lead and eventually to an overestimated 206Pb/238U age at sites with a low U content. The 238U/235U ratios in the studied samples are within the range of 137.74–137.88. Samples with a high uranium content are characterized by a decreasing 238U/235U ratio with a decrease in 207Pb/235U and 206Pb/238U ages. A nonequilibrium 234U/238U ratio in most studied samples furnishes evidence for young (<1.5 Ma) transformation of the Miocene uranium ore, which is responsible for uranium migration and its redeposition.  相似文献   

9.
Basalts in the Southern Rocky Mountains province have been analyzed to determine if any of them are primitive. Alkali plagioclase xenocrysts armored with calcic plagioclase seem to be the best petrographic indicator of contamination. The next best indicator of contamination is quartz xenocrysts armored with clinopyroxene. On the rocks and the region studied, K2O apparently is the only major element with promise of separating primitive basalt from contaminated basalt inasmuch as it constitutes more than 1 % in all the obviously contaminated basalts. K2O: lead (> 4 ppm) and thorium (> 2 ppm) contents and Rb/Sr (> 0.035) are the most indicative of the trace elements studied. Using these criteria, three basalt samples are primitive (although one contains 1.7% K2O) and are similar in traceelement contents to Hawaiian and Eastern Honshu, Japan, primitive basalts.Contamination causes lead isotope ratios, 206Pb/204Pb and 208Pb/204Pb, to become less radiogenic, but it has little or no effect on 87Sr/86Sr. We interpret the effect on lead isotopes to be due to assimilation either of lower crustal granitic rocks, which contain 5–10 times as much lead as basalt and which have been low in U/Pb and Th/Pb since Precambrian times, or of upper crustal Precambrian or Paleozoic rocks, which have lost much of their radiogenic lead because of heating prior to assimilation. The lack of definite effects on strontium isotopes may be due to the lesser strontium contents of granitic crustal rocks relative to basaltic rocks coupled with lack of a large radiogenic enrichment in the crustal rocks.Lead isotope ratios were found to be less radiogenic in plagioclase separates from an obviously contaminated basalt than in the primitive basalts. The feldspar separate that is rich in sodic plagioclase xenocrysts was found to be similar to the whole-rock composition for 206Pb/204Pb and 208Pb/204Pb whereas a more dense fraction probably enriched in more calcic plagioclase phenocrysts is more similar to the primitive basalts in lead isotope ratios.The primitive basalts have: 206Pb/204Pb 18.09–18.34, 207Pb/204Pb 15.5, 208Pb/204Pb 37.6–37.9, 87Sr/86Sr 0.704–0.705. In the primitive basalts from the Southern Rocky Mountains the values of 206Pb/204Pb are similar to values reported by others for Hawaiian and eastern Honshu basalts and abyssal basalts, whereas 208Pb/204Pb tends to be equal to or a little less radiogenic than those from the oceanic localities. 87Sr/86Sr appears to be equal to or a little greater than those of the oceanic localities. These 206Pb/204Pb and 208Pb/204Pb ratios are distinctly less radiogenic and 87Sr/86Sr values are about equal to those reported by others for volcanic islands on oceanic ridges and rises.Publication authorized by the Director, U.S. Geological Survey  相似文献   

10.
The Davis Lake pluton (DLP, ~800 km2) of southwestern Nova Scotia, Canada, part of the large peraluminous South Mountain batholith of ca. 380 Ma (U/Pb zircon, Ar/Ar mica), consists of granite and subordinate topaz–muscovite leucogranite that hosts greisen tin-base metal mineralization. A new Pb–Pb isochron age for leucogranite from the most evolved part of the DLP indicates a crystallization age of 378±3.6 Ma, coincident with other radiometric ages of the DLP (Rb–Sr, Re–Os, Pb–Pb). The intrusion displays a compositional zonation defined by lead and strontium isotopic ratios, as well as some major elements (e.g., Si, F), incompatible trace elements (e.g., Li, Rb, Ta, U, Sn), and elemental ratios (e.g., K/Rb and Nb/Ta). The greisens and the leucogranites that host them are characterized by extreme radiogenic compositions for Pb and Sr, and their chemical-isotopic trends are extensions of the trends displayed by the less evolved granites. The covariations of the isotopic ratios with several major and trace elements and elemental ratios as well as the Pb–Pb and Rb–Sr isochrones indicate that all phases of the intrusion originated from a homogeneous parental magma. The granitoid magma underwent extensive fractional crystallization of feldspars, minor biotite and accessory minerals (monazite, apatite and zircon) in a compositionally zoned magma chamber that was subsequently accompanied by fluid fractionation, during which time the internally derived fluorine-rich fluids modified the Rb/Sr, U/Pb and Th/Pb ratios, leading to distinct variations of 87Sr/86Sr, 206Pb/204Pb, 238U/204Pb and 232Th/204Pb isotopic ratios. These data therefore document the evolution of a granitic magma through magmatic (i.e., crystal fractionation), orthomagmatic (i.e., crystal-fluid fractionation) and hydrothermal (i.e., fluid fractionation) stages that culminated in the formation of a tin-base metal deposit. The Pb isotope data also constrain the source region for the DLP as being Avalonian basement that, by inference, must underlie much of the Meguma Terrane.Editorial responsibility: T.L. Grove  相似文献   

11.
The Qingchengzi orefield in northeastern China, is a concentration of several Pb–Zn, Ag, and Au ore deposits. A combination of geochronological and Pb, Sr isotopic investigations was conducted. Zircon SHRIMP U–Pb ages of 225.3 ± 1.8 Ma and 184.5 ± 1.6 Ma were obtained for the Xinling and Yaojiagou granites, respectively. By step-dissolution Rb–Sr dating, ages of 221 ± 12 Ma and 138.7 ± 4.1 Ma were obtained for the sphalerite of the Zhenzigou Zn–Pb deposit and pyrargyrite of the Ag ore in the Gaojiabaozi Ag deposit, respectively. Pb isotopic ratios of the Ag ore at Gaojiabaozi (206Pb/204Pb = 18.38 to 18.53) are higher than those of the Pb–Zn ores (206Pb/204Pb = 17.66 to 17.96; Chen et al. [Chen, J.F., Yu, G., Xue, C.J., Qian, H., He, J.F., Xing, Z., Zhang, X., 2005. Pb isotope geochemistry of lead, zinc, gold and silver deposit clustered region, Liaodong rift zone, northeastern China. Science in China Series D 48, 467–476.]). Triassic granites show low Pb isotopic ratios (206Pb/204Pb = 17.12 to 17.41, 207Pb/204Pb = 15.47 to 15.54, 208Pb/204Pb = 37.51 to 37.89) and metamorphic rocks of the Liaohe Group have high ratios (206Pb/204Pb = 18.20 to 24.28 and 18.32 to 20.06, 207Pb/204Pb = 15.69 to 16.44 and 15.66 to 15.98, 208Pb/204Pb = 37.29 to 38.61 and 38.69 to 40.00 for the marble of the Dashiqiao Formation and schist of the Gaixian Formation, respectively).Magmatic activities at Qingchengzi and in adjacent regions took place in three stages, and each contained several magmatic pulses: ca. 220 to 225 Ma and 211 to 216 Ma in the Triassic; 179 to 185 Ma, 163 to 168 Ma, 155 Ma and 149 Ma in the Jurassic, as well as ca. 140 to 130 Ma in the Early Cretaceous. The Triassic magmatism was part of the Triassic magmatic belt along the northern margin of the North China Craton produced in a post-collisional extensional setting, and granites in it formed by crustal melting induced by mantle magma. The Jurassic and Early Cretaceous magmatism was related to the lithospheric delamination in eastern China. The Triassic is the most important metallogenic stage at Qingchengzi. The Pb–Zn deposits, the Pb–Zn–Ag ore at Gaojiabaozi, and the gold deposits were all formed in this stage. They are temporally and spatially associated with the Triassic magmatic activity. Mineralization is very weak in the Jurassic. Ag ore at Gaojiabaozi was formed in the Early Cretaceous, which is suggested by the young Rb–Sr isochron age, field relations, and significantly different Pb isotopic ratios between the Pb–Zn–Ag and Ag ores. Pb isotopic compositions of the Pb–Zn ores suggest binary mixing for the source of the deposits. The magmatic end-member is the Triassic granites and the other metamorphic rocks of the Liaohe Group. Slightly different proportions of the two end-members, or an involvement of materials from hidden Cretaceous granites with slightly different Pb isotopic ratios, is postulated to interpret the difference of Pb isotopic compositions between the Pb–Zn–(Ag) and Ag ores. Sr isotopic ratios support this conclusion. At the western part of the Qingchengzi orefield, hydrothermal fluid driven by the heat provided by the now exposed Triassic granites deposited ore-forming materials in the low and middle horizons of the marbles of the Dashiqiao Formation near the intrusions to form mesothermal Zn–Pb deposits. In the eastern part, hydrothermal fluids associated with deep, hidden Triassic intrusions moved upward along a regional fault over a long distance and then deposited the ore-forming materials to form epithermal Au and Pb–Zn–Ag ores. Young magmatic activities are all represented by dykes across the entire orefield, suggesting that the corresponding main intrusion bodies are situated in the deep part of the crust. Among these, only intrusions with age of ca. 140 Ma might have released sufficient amounts of fluid to be responsible for the formation of the Ag ore at Gaojiabaozi.Our age results support previous conclusions that sphalerite can provide a reliable Rb–Sr age as long as the fluid inclusion phase is effectively separated from the “sulfide” phase. Our work suggests that the separation can be achieved by a step-resolution technique. Moreover, we suggest that pyrargyrite is a promising mineral for Rb–Sr isochron dating.  相似文献   

12.
Extreme U and Pb isotope variations produced by disequilibrium in decay chains of 238U and 232Th are found in calcite, opal/chalcedony, and Mn-oxides occurring as secondary mineral coatings in the unsaturated zone at Yucca Mountain, Nevada. These very slowly growing minerals (mm my−1) contain excess 206Pb and 208Pb formed from excesses of intermediate daughter isotopes and cannot be used as reliable 206Pb/238U geochronometers. The presence of excess intermediate daughter isotopes does not appreciably affect 207Pb/235U ages of U-enriched opal/chalcedony, which are interpreted as mineral formation ages.Opal and calcite from outer (younger) portions of coatings have 230Th/U ages from 94.6 ± 3.7 to 361.3 ± 9.8 ka and initial 234U/238U activity ratios (AR) from 4.351 ± 0.070 to 7.02 ± 0.12, which indicate 234U enrichment from percolating water. Present-day 234U/238U AR is ∼1 in opal/chalcedony from older portions of the coatings. The 207Pb/235U ages of opal/chalcedony samples range from 0.1329 ± 0.0080 to 9.10 ± 0.21 Ma, increase with microstratigraphic depth, and define slow long-term average growth rates of about 1.2-2.0 mm my−1, in good agreement with previous results. Measured 234U/238U AR in Mn-oxides, which pre-date the oldest calcite and opal/chalcedony, range from 0.939 ± 0.006 to 2.091 ± 0.006 and are >1 in most samples. The range of 87Sr/86Sr ratios (0.71156-0.71280) in Mn-oxides overlaps that in the late calcite. These data indicate that Mn-oxides exchange U and Sr with percolating water and cannot be used as a reliable dating tool.In the U-poor calcite samples, measured 206Pb/207Pb ratios have a wide range, do not correlate with Ba concentration as would be expected if excess Ra was present, and reach a value of about 1400, the highest ever reported for natural Pb. Calcite intergrown with opal contains excesses of both 206Pb and 207Pb derived from Rn diffusion and from direct α-recoil from U-rich opal. Calcite from coatings devoid of opal/chalcedony contains 206Pb and 208Pb excesses, but no appreciable 207Pb excesses. Observed Pb isotope anomalies in calcite are explained by Rn-produced excess Pb. The Rn emanation may strongly affect 206Pb-238U ages of slow-growing U-poor calcite, but should be negligible for dating fast-growing U-enriched speleothem calcite.  相似文献   

13.
The isotopic composition of Pb in pyrite of the Mindyak orogenic gold deposit located in the Main Ural Fault Zone, the Southern Urals, has been studied by the high-precision MC-ICP-MS method. Orebodies at the deposit are composed of early pyrite and late polysulfide–carbonate–quartz mineral assemblages. The orebodies are localized in olistostrome with carbonaceous clayey-cherty cement. Pyrites from early and late mineral assemblages are close in Pb isotope ratios. For early pyrite 206Pb/204Pb = 18.250–18.336, 207Pb/204Pb = 15.645–15.653, 208Pb/204Pb = 38.179–38.461; while for late pyrite 206Pb/204Pb = 18.102–18.378, 207Pb/204Pb = 15.635–15.646, 208Pb/204Pb = 38.149–38.320. The model parameters μ2 (238U/204Pb = 9.91 ± 2), ω2 (232Th/204Pb = 38.5 ± 4), and 232Th/238U = 3.88 ± 3 indicate that an upper crustal Pb source played a leading role in ore formation. Carbonaceous shale as an olistostrome cement and syngenetic sulfide mineralization are considered to be the main Pb sources of both early and late mineral assemblages. An additional recept in apparently magmatic lead is suggested for the late veinlet mineralization. The involvement of lead from several sources in ore formation is consistent with the genetic model, which assumes a two-stage formation of orebodies at the Mindyak deposit.  相似文献   

14.
We have investigated the potential of hübnerite for U-Pb dating. Hübnerite forms typically at medium to low-temperatures in a wide range of pneumatolytic-hydrothermal mineral deposits, particularly porphyry molybdenum and Sn-specialized granites. Hübnerite from the Sweet Home Mine (Alma, Colorado) formed in a Pb-rich, U-poor environment, but still developed relatively radiogenic Pb isotopic compositions. The low Pbcommon contents in hübnerite (0.075 to 0.155 ppm) demonstrate that Pb is efficiently excluded from the crystal lattice. In contrast, U may substitute for Mn. The U-Pb data of hübnerite scatter. Most of the scatter originates from samples with 206Pb/204Pb values below 50, where Pbblank contributes up to 30% to Pbtotal. Using the least radiogenic galena Pb, samples with 206Pb/204Pb values above 70 have overlapping 206Pb∗/238U and 207Pb∗/235U values and yield a 206Pb/238U age of 25.7 ± 0.3 Ma (2σ). Late stage apatite from the Sweet Home Mine yields a 206Pb/204Pb-238U/204Pb isochron corresponding to an age of 24.8 ± 0.5 Ma (2σ). A comparison of the U-Pb hübnerite ages with literature 40Ar/39Ar ages on earlier sericite and the U-Pb age on later apatite suggests that (i) hübnerite yields accurate U-Pb ages and (ii) the evolution of the Sweet Home mineralization from greisen-type mineralization to medium-temperature hydrothermal vein mineralization took place in a few hundred thousand years at most. Aqueous low-N2-bearing and aqueous inclusions in the dated hübnerite have homogenization temperatures between 325 and 356 °C and moderate salinity (up to 6.7 wt% NaCl equiv.). Thus, hübnerite represents one of the rare examples of a mineral that can be dated accurately and carries petrological information.  相似文献   

15.
目前应用LA-MC-ICPMS分析熔体包裹体Pb同位素,由于没有同时测试U和Th的信号,导致熔体包裹体Pb同位素的研究仅局限于中生代以来的样品。本文应用LA-MC-ICPMS分析了玻璃样品以及存在显著U-Th衰变影响的古老熔体包裹体的Pb同位素组成,评价了U/Pb和Th/Pb分析误差对初始Pb同位素比值校正的影响。实验中以国际玻璃标样NKT-1G为外部标样,采用"标样-样品-标样法"进行仪器漂移和质量歧视校正,结果表明,国际玻璃标样BHVO-2G、TB-1G的208Pb/206Pb和207Pb/206Pb分析精度优于0.30%(2RSD),与推荐值的偏差小于0.30%,然而232Th/206Pb和238U/206Pb分析结果显示了较大分散性(外精度约5.0%)。根据误差传递计算,样品的年龄对初始铅的误差有很大影响。对于古生代以来的样品(年龄小于540 Ma),即使测试的232Th/206Pb和238U/206Pb与真值偏差达到10%,经过U-Th衰变校正后的Pb同位素比值与真值的偏差依然小于0.80%。因此本方法可以将熔体包裹体等地质样品的Pb同位素研究由新生代样品(年龄小于65 Ma)扩展到古生代样品。  相似文献   

16.
The Lovozero alkaline massif—an agpaitic nepheline syenite layered intrusion—is located in the central part of the Kola Peninsula, Russia, and belongs to the Kola ultramafic alkaline and carbonatitic province (KACP) of Devonian age. Associated loparite and eudialyte deposits, which contain immense resources of REE, Nb, Ta, and Zr, constitute a world class mineral district. Previous Sr, Nd, and Hf isotope investigations demonstrated that these rocks and mineral deposits were derived from a depleted mantle source. However, because the Sr, Nd, and Hf abundances in the Kola alkaline rocks are significantly elevated, their isotopic compositions were relatively insensitive to contamination by the underlying crustal rocks through which the intruding magmas passed. Pb occurring in relatively lower abundance in the KACP rocks, by contrast, would have been a more sensitive indicator of an acquired crustal component. Here, we investigate the lead isotopic signature of representative types of Lovozero rocks in order to further characterize their sources. The measured Pb isotopic composition was corrected using the determined U and Th concentrations to the age of the crystallization of the intrusion (376?±?28 Ma, based on a 206Pb/204Pb versus 238U/204Pb isochron and 373?±?9 Ma, from a 208Pb/204Pb versus 232Th/204Pb isochron). Unlike the previously investigated Sr, Nd, and Hf isotopes, the lead isotopic composition plot was well outside the FOZO field. The 206Pb/204Pb values fall within the depleted MORB field, with some rocks having lower 207Pb/204Pb but higher 208Pb/204Pb values. Together with other related carbonatites having both lower and higher 206Pb/204Pb values, the combined KACP rocks form an extended linear array defining either a?~2.5-Ga secondary isochron or a mixing line. The projection of this isotopic array toward the very unradiogenic composition of underlying 2.4–2.5-Ga basaltic rocks of the Matachewan superplume and associated Archean granulite facies country rock provides strong evidence that this old lower crust was the contaminant responsible for the deviation of the Lovozero rocks from a presumed original FOZO lead isotopic composition. Evaluating the presence of such a lower crustal component in the Lovozero rock samples suggests a 5–10% contamination by such rocks. Contamination by upper crustal rock is limited to only a negligible amount.  相似文献   

17.
Epigenetic gold mineralization occurs in the Marmato mining district, within the Calima Terrain of the Setentrional Andes, Colombia. Regional rocks associated with this mineralization include: graphite- and chlorite-schists of the Arquia Complex; metamorphosed during the Cretaceous, Miocene sandstones, shales and conglomerates of the Amagá Formation; as well as pyroclastic rocks (clasts of basalt, andesites and mafic lavas) and subvolcanic andesitic/dacitic bodies of the Combia Formation (9 to 6 Ma). The subvolcanic Marmato stock hosts mesothermal and epithermal low-sulfidation Au–Ag ores in the form of distensional veins, stockwork, and quartz veinlets within brecciated zones. Ore minerals are pyrite, sphalerite and galena with subordinate chalcopyrite, arsenopyrite, pyrrhotite, argentite and native gold/electrum.Sericitized plagioclase from a porphyry dacite yielded a K–Ar age of 5.6 ± 0.6 Ma, interpreted as the age of ore deposition. This is in close agreement with the age of reactivation of the Cauca–Romeral Fault System (5.6 ± 0.4 Ma), which bounds the Calima Terrain. A porphyry andesite–dacite (6.7 ± 0.1 Ma), hosting the Au–Ag veins, shows a measured 87Sr/86Sr between 0.70440 and 0.70460, εNd between + 2.2 and + 3.2 and 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of 18.964 to 19.028; 15.561 to 15.570; and 38.640 to 38.745, respectively. The 87Sr/86Sr and εNd values of rocks from the Arquia Group range from 0.70431 to 0.73511 and − 12.91 to + 10.0, respectively, whereas the corresponding Pb isotopic ratios (206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb) range from 18.948 to 19.652; 15.564 to 15.702; and 38.640 to 38.885, respectively. 87Sr/86Sr and εNd values obtained on sulfides from the gold quartz veins, which occur at shallow and intermediate levels, range from 0.70500 to 0.71210 and from − 1.11 to + 2.40. In the deepest veins, εNd values lie between + 1.25 and + 3.28 and the 87Sr/86Sr of calcite and pyrite fall between 0.70444 and 0.70930. The 206Pb/204Pb, 207Pb/204Pb and 208Pb/204Pb ratios of all mineralization are in the ranges 18.970 to 19.258; 15.605 to 15.726 and 38.813 to 39.208, respectively. Carbonates have an average 87Sr/86Sr ratio of 0.70445, which is within the range of values measured in the host dacite. The Sr isotopic data indicate that carbonic fluids have a restricted hydrothermal circulation within the host igneous body, while the Sr, Pb and Nd isotopic compositions of the sulfides suggest that the fluids not only circulated within the Marmato stock, but also throughout the Arquia Complex, inferring that these rocks offer a potential target for mineral exploration. Based on geological and geochronological evidence, the epizonal Marmato gold ores formed during the Miocene to Pliocene, as a result of cooling of the Marmato stock and reactivation along a crustal-scale fault zone related to thermal processes in an accretionary oceanic–continental plate orogen.  相似文献   

18.
Analyses of the Pb isotopic compositions of plagioclase from 23 samples covering the stratigraphic thickness of the Stillwater Complex indicate a narrow range of apparent initial isotopic compositions (206Pb/ 204Pb=13.95; 207Pb/204Pb=14.95–15.01; 208Pb/204Pb=33.6). The uniformity of our data is in contrast to, but not necessarily contradictory to, other recent investigations which give indications that the complex formed by repeated injection of magmas with at least two distinct compositions that were presumably derived from different source regions. Samples from the Basal series of the complex have consistently higher 207Pb/204Pb ratios, suggesting either minor contamination from adjacent country rocks or a slight distinction between parental magmas. Apparent initial Pb isotopic compositions of the complex are very radiogenic compared to Late Archean model-mantle values, but are nearly identical to initial Pb isotopic compositions found for the the adjacent, slightly older (2.73–2.79 Ga), Late Archean crustal suite in the Beartooth Mountains. Contamination of magmas parental to the Stillwater Complex by the Late Archean crustal suite is rejected for two reasons: (1) Th and U concentrations in Stillwater rocks and plagioclase are very low (about 0.08 and 0.02 ppm respectively), yet Th/U ratios are uniform at about 4, in contrast to the highly variable (2–26) but often high Th/U ratios found for the Late Archean crustal complex; (2) it seems improbable that any contamination process would have adjusted the isotopic compositions of the diverse magmas entering the Stillwater chamber to near-identical values. The preferred hypothesis to explain the Pb isotopic data for the Stillwater Complex and the associated Late Archean crustal suite involves a major Late Archean crust-forming event that resulted in a compositionally complex crust/mantle system with relatively homogeneous and unusual Pb isotopic compositions. The parental magmas of the Stillwater Complex were generated at different levels within this crust/mantle system, before isotopic contrasts could develop by radioactive decay within compositionally discrete reservoirs. This situation limits the utility of all isotopic tracer systems in discriminating among the various mantle and crustal reservoirs that may have affected the final isotopic character of the Stillwater magmas. The late Archean crustal complex and the Stillwater Complex melts were ultimately derived from the same distinct mantle without obvious direct interaction with the Middle to Early Archean crust present in the region.  相似文献   

19.
Garnets from different migmatites and granites from the Damara orogen (Namibia) were dated with the U-Pb technique after bulk dissolution of the material. Measured 206Pb/204Pb ratios are highly variable and range from ca. 21 to 613. Variations in isotope (208Pb/204Pb, 206Pb/204Pb) and trace element (Th/U, U/Nd, Sm/Nd) ratios of the different garnets show that some garnets contain significant amounts of monazite and zircon inclusions. Due to their very low 206Pb/204Pb ratios, garnets from pelitic migmatites from the Khan area yield Pb-Pb ages with large errors precluding a detailed evaluation. However, the 207Pb/206Pb ages (ca. 550–500 Ma) appear to be similar to or older than U-Pb monazite ages (530±1–517±1 Ma) and Sm-Nd garnet ages (523±4–512±3 Ma) from the same sample. It is reasonable to assume that the Pb-Pb garnet ages define growth ages because previous studies are consistent with a higher closure temperature for the U-Pb system in garnet relative to the U-Pb system in monazite and the Sm-Nd system in garnet. For igneous migmatites from Oetmoed, Pb-Pb garnet ages (483±15–492±16 Ma) and one Sm-Nd garnet whole rock age (487±8 Ma) are similar whereas the monazite from the same sample is ca. 30–40 Ma older (528±1 Ma). These monazite ages are, however, similar to monazite ages from nearby unmigmatized granite samples and constrain precisely the intrusion of the precursor granite in this area. Although there is a notable difference in closure temperature for the U-Pb and Sm-Nd system in garnet, the similarity of both ages indicate that both garnet ages record garnet growth in a migmatitic environment. Restitic garnet from an unmigmatized granite from Omaruru yields similar U-Pb (493±30–506±30 Ma) and Sm-Nd (493±6–488±7 Ma) garnet ages whereas the monazite from this rock is ca. 15–25 Ma older (516±1–514±1 Ma). Whereas the monazite ages define probably the peak of regional metamorphism in the source of the granite, the garnet ages may indicate the time of melt extraction. For igneous garnets from granites at Oetmoed, the similarity between Pb-Pb (483±34–474±17 Ma) and Sm-Nd (492±5–484±13 Ma) garnet ages is consistent with fast cooling rates of granitic dykes in the lower crust. Differences between garnet and monazite U-Pb ages can be explained by different reactions that produced these minerals at different times and by the empirical observation that monazite seems resistant to later thermal re-equilibration in the temperature range between 750 and 900 °C (e.g. Braun et al. 1998). For garnet analyses that have low 206Pb/204Pb ratios, the influence of high- inclusions is small. However, the relatively large errors preclude a detailed evaluation of the relationship between the different chronometers. For garnet with higher 206Pb/204Pb ratios, the overall similarity between the Pb-Pb and Sm-Nd garnet ages implies that the inclusions are not significantly older than the garnet and therefore do not induce a premetamorphic Pb signature upon the garnet. The results presented here show that garnet with low 238U/204Pb ratios together with Sm-Nd garnet data and U-Pb monazite ages from the same rock can be used to extract geologically meaningful ages that can help to better understand tectonometamorphic processes in high-grade terranes.Editorial responsibility: J. Hoefs  相似文献   

20.
The weathered surface expression of the Lady Loretta lead-zinc-silver deposit outcrops almost continuously over a distance of about 4 km. Lead isotope ratios have been determined for samples, some of which contain > 4000 ppm Pb, from geochemically anomalous areas in order to assign drilling priorities to the anomalies.Twelve of the 43 samples analyzed contain isotopically homogeneous lead with ratios (207Pb/206Pb 0.9532–0.9549) similar to the expected targets for major ore deposits in the Mount Isa-McArthur River metallogenic province (207Pb/206Pb 0.955–0.962). Three main zones of interest can be outlined on the basis of lead isotopic data. The top priority is assigned to a 100-m-long section of the ironstone which coincides with the known outcrop of the ore. Lower priority for drilling is given to the two other zones which outcrop over smaller areas and have more radiogenic lead in their immediate surroundings. Several samples with anomalously high lead contents (> 1000 ppm) contain more radiogenic lead (207Pb/206Pb < 0.950) which was most likely derived from the weathering country rocks by supergene leaching and redeposition. Of the 22 samples containing ≥ 380 ppm Pb, lead isotopic analyses would have reduced the number deserving further attention to 10. Lead isotopic analyses in the early stages of exploration could have assisted in minimizing exploration expenditure at Lady Loretta.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号