Uranium-series chronology for sediments of Lake Hovsgol, Mongolia, and the 1-Ma records of uranium and thorium isotopes from the HDP-04 drill core

Uranium and thorium isotopes in an 81-m long sediment core (HDP-04) of Lake Hovsgol, Mongolia, were measured to investigate their downcore distributions and to explore potential linkage to paleoenvironmental changes. Three-dimensional isochron techniques using isotope-ratio diagrams in ²³⁸U–²³⁴U–²³⁰Th–²³²Th system presented by Ludwig and Titterington were applied to age date the lake sediments at the depths of 11.42, 14.71 and 14.83 m in the HDP-04 section, the estimated ages of these horizons are 66 ± 8, 122 ± 11 and 128 ± 22 ka, respectively. The ²³⁸U concentration throughout the entire section fluctuated by a factor of 12, ranging from 19.9 to 232.1 mBq/g with anomalously high ²³⁸U peak at 23.8 m in depth, while the ²³²Th concentration varied only by a factor of about two between 24.3 and 54.0 mBq/g. The discrimination of the bulk ²³⁸U into authigenic and terrigenous ²³⁸U fractions was attempted, based on the measured ²³²Th as a correction index for terrigenous materials. In the upper 24 m corresponding to the last 250 ka, the authigenic ²³⁸U was higher in interglacials and lower in glacials. This depth profile of authigenic ²³⁸U contents was almost identical pattern with that found in a sediment core (VER98-1-6) from the Academician Ridge, Lake Baikal. Further, this profile can be correlated well with that of photosynthetic pigment contents, one of proxies of paleoproductivity, suggesting that the variation of authigenic ²³⁸U contents were associated with the environmental change around Lake Hovsgol.     

U‐Th Zircon Dating by Laser Ablation Single Collector Inductively Coupled Plasma‐Mass Spectrometry (LA‐ICP‐MS)

Zircon crystals in the age range of ca. 10–300 ka can be dated by ²³⁰Th/²³⁸U (U‐Th) disequilibrium methods because of the strong fractionation between Th and U during crystallisation of zircon from melts. Laser ablation inductively coupled plasma‐mass spectrometry (LA‐ICP‐MS) analysis of nine commonly used reference zircons (at secular equilibrium) and a synthetic zircon indicates that corrections for abundance sensitivity and dizirconium trioxide molecular ions (Zr₂O₃⁺) are critical for reliable determination of ²³⁰Th abundances in zircon. When corrected for abundance sensitivity and interferences, mean activity ratios of (²³⁰Th)/(²³⁸U) for nine reference zircons analysed on five different days averaged 0.995 ± 0.023 (95% confidence weighted by data‐point uncertainty only, MSWD = 1.6; n = 9), consistent with their U‐Pb ages > 4 Ma that imply equilibrium for all intermediate daughter isotopes (including ²³⁰Th) within the ²³⁸U decay chain. U‐Th zircon ages generated by LA‐ICP‐MS without mitigating (e.g., by high mass resolution) or correcting for abundance sensitivity and molecular interferences on ²³⁰Th are potentially unreliable. To validate the applicability of LA‐ICP‐MS to this dating method, we acquired data from three late Quaternary volcanic units: the 41 ka Campanian Ignimbrite (plutonic clasts), the 161 ka Kos Plateau Tuff (juvenile clasts) and the 12 ka Puy de Dôme trachyte lava (all eruption ages by Ar/Ar, with zircon U‐Th ages being of equal or slightly older). A comparison of the corrected LA‐ICP‐MS results with previously published secondary ion mass spectrometry (SIMS) data for these rocks shows comparable ages with equivalent precision for LA‐ICP‐MS and SIMS, but much shorter analysis durations (~ 2 min vs. ~ 15 min) per spot with LA‐ICP‐MS and much simpler sample preparation. Previously undated zircons from the Yali eruption (Kos‐Nisyros volcanic centre, Greece) were analysed using this method. This yielded a large age spread (~ 45 to > 300 ka), suggesting significant antecryst recycling. The youngest zircon age (~ 45 ± 10 ka) provides a reasonable maximum estimate for the eruption age, in agreement with the previously published age using oxygen isotope stratigraphy (~ 31 ka).     

U-Th dating of carbonate platform and slope sediments

Absolute chronology of marine sediment beyond the ¹⁴C age range provides a test for models of climate change and has many other applications. U-Th techniques have been used for such chronology by dating corals, but extending these techniques to marine sediment is complicated by the presence of significant initial ²³⁰Th—both in detrital material and scavenged from seawater. In this study, we investigate four methods of solving the initial ²³⁰Th problem for a particular type of marine sediment—the aragonite-rich sediments of carbonate platforms and slopes. Bulk sediment U-Th analyses can be corrected for initial Th to yield ages with ≈2 to 3 kyr precision for highstand periods when sediment aragonite contents are particularly high. Uncertainty on the corrections causes inadequate precision for sediment from other periods, however. Removal of scavenged Th before analysis would enable a dramatic increase in this precision but has not proved successful despite a range of chemical leach approaches. Using heavy liquids to separate the various carbonate minerals found in Bahamas sediment enables an isochron approach to correct for initial Th, but the presence of initial Th from two sources requires correction or removal of one source of initial Th before the other is deconvolved by the isochron. Quantitative removal of detrital material before isochron analysis proves a successful approach. Such isochron data demonstrate that, although sediment remains closed to U-Th on a centimetre scale, nuclides are moved from grain to grain by α-recoil. Such intergrain exchange is expected to be observed in all sediments containing mineral grains with different U concentrations. Measured ²³⁴U/²³⁸U allows the recoil movement to be corrected and results in isochron ages with precision sometimes as low as 3 kyr. The accuracy of this approach has been proved by dating samples within the ¹⁴C age range. Sediments spanning the penultimate deglaciation have also been dated. After a small correction for bioturbation, the age for this event is found to be 135.2 ± 3.5 ka. This date is ≈8 kyr before the peak in northern hemisphere insolation and suggests that deglaciation is initiated by a mechanism in the southern hemisphere or tropics. This isochron approach shows considerable promise for dating of sediments older than this event, which will provide further information about the timing and mechanisms of global climate change.     

U-series evidence for crustal involvement and magma residence times in the petrogenesis of Parinacota volcano, Chile

In this study, we present Th–U disequilibria as well as radiogenic and trace element data for recent volcanic rocks from the Nevados de Payachata volcano which erupted through ∼70 km of continental crust in the Central Volcanic Zone of the Andes (18°S, 69°W). Both lavas and mineral separates were analyzed by mass spectrometry for ²³⁸U–²³⁰Th disequilibria. The lavas are characterized either by ²³⁰Th enrichment or depletion relative to its parent nuclide ²³⁸U. Mineral separates are used to derive U–Th isochron ages and these ages compare favorably with inferred stratigraphic ages or K–Ar ages, although in one case the U–Th age is significantly older than the stratigraphic age. Despite relatively constant Sr, Nd, and Pb isotope ratios, the lavas display inverse trends in ²³⁰Th/²³⁸U versus Ce/Yb or Ba/Hf diagrams. These trends cannot be interpreted by simple two-component mixing. Rather, there must be three (and perhaps four components) involved in the genesis of the Parinacota lavas. A mantle wedge, a slab fluid, and a lower crustal component can be identified. A sediment component is more difficult to detect as it is difficult to decipher its signature because of the strong crustal influence. The existence of binary arrays can be explained by variable amounts of crustal material. The process of crust–mantle interaction must have been short enough to preserve U–Th disequilibrium (<300 ka). Received: 21 April 1999 / Accepted: 11 March 2000     

Crystallization history of rhyolites at Long Valley, California, inferred from combined U-series and Rb-Sr isotope systematics

In this study, we present ⁸⁷Rb/⁸⁶Sr and ²³⁰Th/²³⁸U isotope analyses of glasses and phenocrysts from postcaldera rhyolites erupted between 150 to 100 ka from the Long Valley magmatic system. Both isotope systems indicate complex magma evolution with preeruptive mineral crystallization and magma fractionation, followed by extended storage in a silicic magma reservoir. Glass analyses yield a Rb-Sr isochron of 257 ± 39 ka, which can be explained by a feldspar-fractionation event ∼150 ky before eruption. Individual feldspar-glass pairs confirm this age result. A mineral ²³⁰Th-²³⁸U isochron in a low-silica rhyolite from the Deer Mountain Dome defines an age of 236 ± 1 ka, but the glass and whole rock do not lie on the isochron. U-Th fractionation of the rocks is controlled by the accessory minerals zircon and probably allanite, which crystallized at 250 ± 3 ka and 187 ± 9 ka, respectively. All major mineral phases contain accessory mineral phases; therefore, the mineral isochron represents a mixture of zircon and allanite populations. A precision of ±1 ka for the mixing array implies that the minor phases must have crystallized within this timescale. Longer periods of crystal growth would cause the mixing array to be less well defined. U-series data from other low- and high-silica rhyolites indicate younger accessory mineral crystallization events at ∼200 and 140 ka, probably related to the thermal evolution of the magma reservoir. These crystallization events are, however, only documented by the accessory minerals and had no further influence on bulk magma compositions. We interpret the indistinguishable age results from both isotope systems (∼250 ka) to record the fractionation of small magma batches by filter pressing from a much larger underlying magma volume, followed by physical isolation and extended storage at the top of the magma reservoir for up to 150 ky.     

Th/U/U and Pa/U ages from a single fossil coral fragment by multi-collector magnetic-sector inductively coupled plasma mass spectrometry

The ²³⁰Th/²³⁴U/²³⁸U age dating of corals via alpha counting or mass spectrometry has significantly contributed to our understanding of sea level, radiocarbon calibration, rates of ocean and climate change, and timing of El Nino, among many applications. Age dating of corals by mass spectrometry is remarkably precise, but many samples exposed to freshwater yield inaccurate ages. The first indication of open-system ²³⁰Th/²³⁴U/²³⁸U ages is elevated ²³⁴U/²³⁸U_initial values, very common in samples older than 100,000 yr. For samples younger than 100,000 yr that have ²³⁴U/²³⁸U_initial values close to seawater, there is a need for age validation. Redundant ²³⁰Th/²³⁴U/²³⁸U and ²³¹Pa/²³⁵U ages in a single fossil coral fragment are possible by Multi-Collector Magnetic Sector Inductively Coupled Plasma Mass Spectrometry (MC-MS-ICPMS) and standard anion exchange column chemistry, modified to permit the separation of uranium, thorium, and protactinium isotopes from a single solution. A high-efficiency nebulizer employed for sample introduction permits the determination of both ²³⁰Th/²³⁴U/²³⁸U and ²³¹Pa/²³⁵U ages in fragments as small as 500 mg. We have obtained excellent agreement between ²³⁰Th/²³⁴U/²³⁸U and ²³¹Pa/²³⁵U ages in Barbados corals (30 ka) and suggest that the methods described in this paper can be used to test the ²³⁰Th/²³⁴U/²³⁸U age accuracy.Separate fractions of U, Th, and Pa are measured by employing a multi-dynamic procedure, whereby ²³⁸U is measured on a Faraday cup simultaneously with all minor isotopes measured with a Daly ion counting detector. The multi-dynamic procedure also permits correcting for both the Daly to Faraday gain and for mass discrimination during sample analyses. The analytical precision of ²³⁰Th/²³⁴U/²³⁸U and ²³¹Pa/²³⁵U dates is generally better than ±0.3% and ±1.5%, respectively (2 Relative Standard deviation [RSD]). Additional errors resulting from uncertainties in the decay constant for ²³¹Pa and from undetermined sources currently limit the ²³¹Pa/²³⁵U age uncertainty to about ±2.5%. U isotope data and ²³⁰Th/²³⁴U/²³⁸U ages agree with National Institute of Standards and Technology (NIST) reference materials and with measurements made by Thermal Ionization Mass Spectrometry (TIMS) in our laboratory.     

A history of violence: magma incubation,timing and tephra distribution of the Los Chocoyos supereruption (Atitlán Caldera,Guatemala)

The climactic Los Chocoyos (LCY) eruption from Atitlán caldera (Guatemala) is a key chronostratigraphic marker for the Quaternary period given the extensive distribution of its deposits that reached both the Pacific and Atlantic Oceans. Despite LCY tephra being an important marker horizon, a radioisotopic age for this eruption has remained elusive. Using zircon (U–Th)/He geochronology, we present the first radioisotopically determined eruption age for the LCY of 75 ± 2 ka. Additionally, the youngest zircon crystallization ²³⁸U–²³⁰Th rim ages in their respective samples constrain eruption age maxima for two other tephra units that erupted from Atitlán caldera, W-Fall (130 ⁺¹⁶/₋₁₄ ka) and I-Fall eruptions (56 ^+8.2/_−7.7 ka), which under- and overlie LCY tephra, respectively. Moreover, rim and interior zircon dating and glass chemistry suggest that before eruption silicic magma was stored for >80 kyr, with magma accumulation peaking within ca. 35 kyr before the LCY eruption during which the system may have developed into a vertically zoned magma chamber. Based on an updated distribution of LCY pyroclastic deposits, a new conservatively estimated volume of ~1220 ± 150 km³ is obtained (volcanic explosivity index VEI > 8), which confirms the LCY eruption as the first-ever recognized supereruption in Central America.     

Can 234U–230Th dating be used to date large semi‐arid tufas? Challenges from a study in the Naukluft Mountains,Namibia

The large, extensive tufa deposits of the semi‐arid Naukluft Mountains, Namibia are potentially important palaeoenvironmental indicators in an area with few proxy records. Tufas are reliable indicators of increased moisture availability, and have been shown to be amenable to ²³⁴U–²³⁰Th dating, although two challenges are detrital contamination and open‐system behaviour. Densely cemented tufa facies are good candidates for dating, minimising these problems. We report attempts to date five densely‐cemented units, which are only found rarely within the Naukluft deposits. We applied a detailed methodology using multiple subsample analysis, measurement of insoluble residues, application of ‘isochron’ mixing lines, and attempted open‐systems modelling, alongside observations of micromorphology and cathodoluminescence in order to assess the validity of any obtained dates. Surprisingly, densely cemented tufas were found not always to be suitable for dating. Two units contained detrital contamination, which could not be corrected for using a single leachate correction or ‘isochron’ methods. Two units contained ‘excess ²³⁰Th’. This could result under a closed‐system if initial (²³⁴U/²³⁸U) was sufficiently high. Alternatively this may be the result of open‐system behaviour, and loss of uranium, or incorporation of initial unsupported ²³⁰Th, which render samples unsuitable for ²³⁴U–²³⁰Th dating. Micromorphological appearance and cathodoluminescence behaviour are used to explore these possibilities. This study exemplifies the need for careful sample selection, and highlights the importance of analysing multiple subsamples from any tufa sample. The detailed methodology applied proves to be a powerful tool for identifying the range of problems that can be encountered when selecting suitable candidate samples for successful dating. It also shows that semi‐arid tufa sequences may contain very little material suitable for dating. A reliable age of c 80 ka was obtained for a banded unit within a large fluvial barrage, with less reliable dates suggesting tufa deposition during times since >350 ka through to the late Holocene. Copyright © 2010 John Wiley & Sons, Ltd.     

Precise two chronometer dating of Pleistocene travertine: The Th/U and Raex/Ra(0) approach

In order to determine the geochemical evolution of a freshwater limestone cave system located in central Switzerland (Hell Grottoes at Baar/Zug,) young postglacial tufaceous limestone and travertine precipitates were investigated using the ²³⁰Th/²³⁴U ingrowth system. Additional analyses of further radionuclides within the ²³⁸U decay chain, i.e. ²²⁶Ra and ²¹⁰Pb, showed that the Th/U chronometer started with insignificant inherited ²³⁰Th over the entire formation period of the travertine setting (i.e. ²³⁰Th(0)=0). A contribution from detrital impurities with ²³⁰Th/²³⁴U in secular equilibrium could be precisely subtracted by applying isochron dating of cogenetic phases and recently formed travertine. The resulting precise ²³⁰Th/²³⁴U formation ages were found to be consistent with the geological stratigraphy and were furthermore used to demonstrate the applicability of the next geologically important chronometer in the ²³⁸U-decay series, based on decay of excess ²²⁶Ra normalized to the initial, i.e.²²⁶Ra_ex/²²⁶Ra(0). This system is suitable for dating phases younger than 7000 yr when the correction of a detritus component increasingly limits the precision of the ²³⁰Th/²³⁴U chronometer. Analytical solutions of the coupled ²³⁴U/²³⁰Th/²²⁶Ra radionuclide system predicted that the ²²⁶Ra_ex/²²⁶Ra(0) chronometer is independent of the actual ²³⁰Th activity build up from decay of ²³⁴U, if the systems starts with zero inherited ²³⁰Th(0). The data set confirmed this hypothesis and showed furthermore that the initially incorporated ²²⁶Ra excess must have remained almost uniform in all limestone over a period of at least 7000 yr, i.e. 4–5 half-lives of ²²⁶Ra. This is concluded because (i) the ²²⁶Ra_ex/²²⁶Ra(0) ages agreed well with those derived from ²³⁰Th/²³⁴U, (ii) all data plot within uncertainty on the ²²⁶Ra_ex/²²⁶Ra(0) decay curve and (iii) the atomic Ba/Ca ratio was found to be constant in the travertine material independent of the sample ages. Provided that such boundary conditions hold, ²²⁶Ra_ex/²²⁶Ra(0) should be applicable to materials which are suitable for ²³⁰Th/²³⁴U dating in sedimentology and oceanography, i.e. travertine, corals, phosphorites, etc., and should strongly support ²³⁰Th/²³⁴U for samples that have been formed a few thousand years ago.     

Uranium-series dating of pedogenic silica and carbonate, Crater Flat, Nevada

A ²³⁰Th-²³⁴U-²³⁸U dating study on pedogenic silica-carbonate clast rinds and matrix laminae from alluvium in Crater Flat, Nevada was conducted using small-sample thermal-ionization mass spectrometry (TIMS) analyses on a large suite of samples. Though the ²³²Th content of these soils is not particularly low (mostly 0.1-9 ppm), the high U content of the silica component (mostly 4-26 ppm) makes them particularly suitable for ²³⁰Th/U dating on single, 10 to 200 mg totally-digested samples using TIMS. We observed that (1) both micro- (within-rind) and macro-stratigraphic (mappable deposit) order of the ²³⁰Th/U ages were preserved in all cases; (2) back-calculated initial ²³⁴U/²³⁸U fall in a restricted range (typically 1.67±0.19), so that ²³⁴U/²³⁸U ages with errors of about 100 kyr (2σ) could be reliably determined for the oldest, 400 to 1000 ka rinds; and (3) though 13 of the samples were >350 ka, only three showed evidence for an open-system history, even though the sensitivity of such old samples to isotopic disruption is very high. An attempt to use leach-residue techniques to separate pedogenic from detrital U and Th failed, yielding corrupt ²³⁰Th/U ages. We conclude that ²³⁰Th/U ages determined from totally dissolved, multiple sub-mm size subsamples provide more reliable estimates of soil chronology than methods employing larger samples, chemical enhancement of ²³⁸U/²³²Th, or isochrons.     

Columbite SN3: A New Potential Reference Material for U-Pb Dating by LA-ICP-MS

Columbite-tantalite LA-ICP-MS U-Pb dating is a fast and useful method to determine the age of rare-metal deposits and fingerprint the provenance of columbite-tantalite ore concentrates. Accurate LA-ICP-MS U-Pb dating requires matrix-matched reference materials. We analysed three columbite-tantalite samples (SN3, HND and RL2) from China using ID-TIMS and LA-ICP-MS to assess their potential as reference materials for in situ U-Pb dating. Coltan 139 and these three columbite-tantalite samples with variable compositions yielded internally consistent LA-ICP-MS U-Pb ages when using each other for calibration and the weighted mean ²⁰⁶Pb/²³⁸U ages are comparable to respective ID-TIMS ages. Composition-dependent U-Pb fractionation seems to be insignificant under the LA-ICP-MS conditions used. Sample SN3 has a low percentage of heterogeneity for ²⁰⁶Pb/²³⁸U ages (4%) with low common Pb contributions (f₂₀₆ < 1%) and shows a good potential in calibrating unknown samples as primary reference material for LA-ICP-MS analysis. Samples RL2 and HND have altered sections characterised by high LREE contents, flat LREE patterns and old ²⁰⁶Pb/²³⁸U apparent ages, and are not suited as reference materials. The low ²⁰⁷Pb/²⁰⁶Pb intercepts for samples RL2 and HND lack geological meaning but provide strong evidence that the disturbed U-Pb systematics with anomalous apparent ²⁰⁶Pb/²³⁸U ages is a secondary feature.     

Uranium geochemistry and dating of Pacific island apatite

Uranium-series disequilibrium dating of island phosphate deposits is evaluated in terms of known associated coral ages, uranium geochemistry, and stratigraphic sequences as well as the concordance between the geochronometers ²³⁴U/²³⁸U, ²³⁰Th/²³⁴U and ²²⁶Ra/²³⁸U. U(VI) is the predominant oxidation state of uranium in island phosphorites and by analogy to the youngest surficial deposits, most of the uranium initially bound is in the form of U(VI) sorbed by surfaces from seawater. Insular deposits contain more organic matter than even very young ocean floor samples and this leads to a greater probability of reduction of available recoil uranium than occurs in marine deposits. As a consequence, R(VI) ? R(T) ? R(VI), where R represents the ²³⁴U/²³⁸U activity ratio. This situation is completely opposite from that observed for marine-origin phosphorites. We determined that a fraction of U(VI) in ancient insular phosphorites is very labile and lost to alkaline carbonate solutions with a uranium activity ratio even more depleted in ²³⁴U than the bulk R(VI).Most younger samples appear to have no more discordance between ²³⁴U/²³⁸U, ²³⁰Th/²³⁴U and ²²⁶Ra/²³⁸U than marine phosphorites of similar apparent age. Young, surficial atoll-rim apatite cements and unconsolidated phosphorites date in the range of 1500–8000 years B.P., consistent with the concept of partial submergence of low-lying coral islands prior to 2000 years B.P. Sub-surficial samples in the same environment date older at about 20,000 years B.P. Violation of the closed system assumption occurs in at least 6 out of 13 ancient (> 800,000 year) samples. Uranium-series disequilibrium dating of insular apatite shows some promise as a recorder of climatic/sea level events, but the assumptions necessary for valid ages must be carefully evaluated for each occurrence.     

Low-T eclogite in the Dabie terrane of China: petrological and isotopic constraints on fluid activity and radiometric dating

While extensive studies have demonstrated fluid release during subduction of oceanic crust, little attention has been paid to fluid activity during subduction and exhumation of continental crust. Abundant occurrence of quartz veins within eclogites in the Dabie-Sulu orogenic belt of China provides us with an opportunity to study the origin and role of vein-forming fluids with respect to heat and mass transfer during ultrahigh pressure (UHP) metamorphism and its relevant processes. This study focuses on kyanite-quartz vein that occurs as polycrystalline aggregates within the low-T eclogite in the Dabie terrane, which are interpreted as pseudomorphs after former porphyroblasts of lawsonite. Coesite pseudomorphs were found for the first time in eclogite garnet, resulting in a revised estimate of peak P–T conditions at 670°C and 3.3 GPa for the eclogite and thus upgrading the high-P unit to an UHP unit. On the basis of the relationship between calculated P–T path and metamorphic reactions as well as the absence of foliation texture, and undulose extinction of quartzes in the vein, we conclude that lawsonite breakdown into kyanite–quartz–zoisite assemblage took place at the onset of exhumation subsequent to peak pressure. Retrograde metamorphism caused O and H isotope disequilibria between some of the minerals, but the fluid for retrograde reactions was internally buffered in stable isotope compositions. Zircon U–Pb dating and whole-rock Nd–Sr isotope analyses indicate that eclogite protolith is the paleoceanic basalt that was derived from the depleted mantle by magmatism at about 1.8 to 1.9 Ga but experienced hydrothermal alteration by surface waters. The altered basalt underwent UHP metamorphism in the Triassic that caused fluid release for zircon growth/overgrowth not only at about 242±3 Ma prior to the onset of peak pressure but also at about 222±4 Ma during decompression dehydration by lawsonite breakdown and hydroxyl exsolution in the low-T/UHP eclogite. Consistent ages of 236.1±4.2 Ma and 230±7 Ma were obtained from mineral Sm–Nd and Rb–Sr isochron dating, respectively, indicating attainment and preservation of Nd and Sr isotope equilibria during the Triassic UHP eclogite-facies metamorphism. Ar–Ar dating on paragonite from the eclogite gave consistent plateau and isochron ages of 241.3±3.1 Ma and 245.5±9.8 Ma, respectively, which are interpreted to date paragonite crystallization during the prograde eclogite-facies metamorphism. The timing of peak UHP metamorphism for the low-T eclogite is constrained at sometime prior to 236.1±4.2 Ma. Thus the termination age of peak UHP metamorphism may be different in different slices of deep-subducted slab.     

粤北长江铀矿田花岗岩独居石U-Pb同位素定年及其地质意义

长江铀矿田位于诸广山复式岩体中南部,是典型的花岗岩型铀矿田.前人采用锆石U-Pb定年方法对赋矿花岗岩进行了年代学研究,但由于全岩和锆石铀含量较高,锆石往往发生了蜕晶化,可能导致锆石U-Pb定年数据散乱,影响锆石U-Pb年龄的可靠性.独居石是花岗岩中广泛存在的含铀副矿物,铀和钍含量均较高,可达10000×10-6,普通铅...     

Timing of the Last-Interglacial High Sea Level on the Seychelles Islands, Indian Ocean

Corals from the Seychelles Islands, Indian Ocean, occur mainly as small coralline algae–vermetid remnants found in cavities adhering to the rock surface, and they rarely attain more than 2 m²in area. Samples ofGoniastreaandPoritesfrom elevations between 1.7 and 6 m above present mean sea level were dated by TIMS²³⁸U–²³⁴U–²³⁰Th techniques. The ages from well-preserved corals lie between 131,000 and 122,000 yr B.P., in agreement with most other observations of the last-interglacial sea level. Field evidence and dating from high marine limestones from two sections at La Digue Island indicate a period of coral buildup until 131,000 yr B.P., followed by a drop in sea level between 131,000 and 122,000 yr B.P.     

Plume-lithosphere interaction beneath Mt. Cameroon volcano, West Africa: Constraints from U-Th-Ra and Sr-Nd-Pb isotope systematics

Precise measurements of ²³⁸U-²³⁰Th-²²⁶Ra disequilibria in lavas erupted within the last 100 yr on Mt. Cameroon are presented, together with major and trace elements, and Sr-Nd-Pb isotope ratios, to unravel the source and processes of basaltic magmatism at intraplate tectonic settings. All samples possess ²³⁸U-²³⁰Th-²²⁶Ra disequilibria with ²³⁰Th (18-24%) and ²²⁶Ra (9-21%) excesses, and there exists a positive correlation in a (²²⁶Ra/²³⁰Th)-(²³⁰Th/²³⁸U) diagram. The extent of ²³⁸U-²³⁰Th-²²⁶Ra disequilibria is markedly different in lavas of individual eruption ages, although the (²³⁰Th/²³²Th) ratio is constant irrespective of eruption age. When U-series results are combined with Pb isotope ratios, negative correlations are observed in the (²³⁰Th/²³⁸U)-(²⁰⁶Pb/²⁰⁴Pb) and (²²⁶Ra/²³⁰Th)-(²⁰⁶Pb/²⁰⁴Pb) diagrams. Shallow magma chamber processes like magma mixing, fractional crystallization and wall rock assimilation do not account for the correlations. Crustal contamination is not the cause of the observed isotopic variations because continental crust is considered to have extremely different Pb isotope compositions and U/Th ratios. Melting of a chemically heterogeneous mantle might explain the Mt. Cameroon data, but dynamic melting under conditions of high D_U and D_U/D_Th, long magma ascent time, or disequilibrium mineral/melt partitioning, is required. The most plausible scenario to produce the geochemical characteristics of Mt. Cameroon samples is the interaction of melt derived from the asthenospheric mantle with overlying sub-continental lithospheric mantle which has elevated U/Pb (>0.75) and Pb isotope ratios (²⁰⁶Pb/²⁰⁴Pb > 20.47) due to late Mesozoic metasomatism.     

Chronological and geochemical study of lavas from the Chaîne des Puys,Massif Central,France: Evidence for crustal contamination

Datations of ancient lavas from the Chaîne des Puys through the ²³⁰Th-²³⁸U radioactive disequilibrium method confirm the eruption of several basaltic or slightly differentiated lavas around 40,000 years ago. The study of (²³⁰Th/²³²Th)₀ initial ratios of these lava flows clearly demonstrates the influence of a crustal contamination of magmas superimposed to crystal fractionation. This contamination probably affects many trace elements, in particular, U, Th and Sr. A model based on the (²³⁰Th/²³²Th)₀ initial ratio variations of non-contaminated lavas permits to consider that the first eruptions in the Chaîne des Puys could have occurred about 100,000 years ago.     

内蒙古道伦达坝铜钨锡矿床LA-ICP-MS锆石和锡石U-Pb年龄及其地质意义

道伦达坝矿床位于大兴安岭南段,是一个铜钨锡矿床,其铜、钨、锡储量均达中型。矿体呈脉状,主要产于二叠系砂板岩中的断裂破碎带中,华力西期黑云母花岗岩中的断裂破碎带中亦赋存有矿体。文章选取2件石英-萤石-白云母-电气石-锡石-黑钨矿阶段的矿石样品对其中的进行了LA-ICP-MS U-Pb定年,获得2件样品的~(207)Pb/~(206)Pb-~(238)U/~(206)Pb谐和年龄分别为(134.7±6.6)Ma(MSWD=1.4)和(136.8±7.4)Ma(MSWD=1.7),~(206)Pb/~(207)Pb-~(238)U/~(207)Pb等时线年龄分别为(132±12)Ma(MSWD=0.76)和(135±13)Ma(MSWD=0.9)。锡石定年结果表明,道伦达坝矿床形成于早白垩世。对矿区外围张家营子岩体中的斑状细粒花岗岩进行了LA-ICP-MS锆石U-Pb测年,获得的~(206)Pb/~(238)U加权平均年龄为(135±1)Ma(MSWD=1.3),该岩体的形成年龄与道伦达坝矿床的成矿年龄在误差范围内一致。本次定年结果表明道伦达坝矿床形成于早白垩世,与同期的花岗质岩浆活动有密切的成因联系,该矿床属于与花岗岩有关的岩浆热液脉型矿床。     

中国东部全新世火山的镭-钍同位素年代学

活火山是指1万年来有过喷发历史的全新世火山。火山的高分辨年代学对火山灾害评估和火山分类具有重要意义。对于缺乏历史记载的全新世火山,直接对火山岩进行同位素定年很困难。本文利用具有高时间分辨率的镭-钍-铀非平衡确定中国东部年轻火山的年龄。根据镭-钍-铀同位素,海南岛的马鞍岭和雷虎岭是全新世火山(马鞍岭:4.3ka;雷虎岭:4.7ka);镜泊湖火山(4.9ka)也是全新世火山;龙岗火山存在晚更新世和全新世活动(7.0ka,15.0ka);大兴安岭阿尔山和诺敏河Ra/Th非平衡消失但~(230)Th/~(238)U非平衡显著,属于晚更新世喷发(阿尔山:63ka;诺敏河:71ka)。海南岛的马鞍岭火山、雷虎岭火山和东北地区的龙岗火山、镜泊湖火山,是4座活火山。至于东北地区的阿尔山和诺敏河火山是否是活火山,有待测试更多样品的Ra/Th同位素。五大连池老黑山和火烧山有历史喷发记录,这与它们都存在显著Ra/Th非平衡一致。五大连池老黑山和火烧山的岩浆滞留年龄分别小于4.2ka和3.2ka,岩浆上升速率 18～23m/y。     

铀系组分法测定年青火山岩年龄的研究

铀系组分法是测定火山岩不同组分中的２３０Ｔｈ／２３２Ｔｈ值和２３８Ｕ／２３２Ｔｈ值、计算年龄的方法。岩石中的各组分是用磁选或浮选分离的。经过论证，组分法与等时线方法是等价的，但不需要从全岩中精选纯的单矿物，不会发生铀和钍同位素的分馏。根据组分法模式测定了云南腾冲盆地北来凤山、老龟坡山和马鞍山火山岩样品的年龄，分别为０．１１ＭａＢ．Ｐ．、５１０００。Ｂ．Ｐ．和２５０００ａＢ．Ｐ，与地层顺序相吻合。组分法对于年青火山岩定年有着极大的潜力。