Applications of near-infrared FT-Raman spectroscopy in metamict and annealed zircon: oxidation state of U ions

We report a near-infrared Fourier-transform (FT) Raman spectroscopic method to characterize the electronic transitions of U ions and the alpha-decay damage in natural zircon. The application is demonstrated by analyzing metamict and annealed zircons from Sri Lanka. The data from crystalline zircon reveal a relatively sharp spectral feature appearing near 2733 cm^–1 in Stokes spectra with a laser excitation of 1064 nm. The feature is assigned as signals related to the previously reported U⁵⁺ absorption near 6668 cm^–1. With increasing self-irradiation dose, the feature shows a systematic decrease in intensity, accompanied by a gradual development of a broad feature between 3000 and 3400 cm^–1. On heating for 1 h, the U⁵⁺ feature shows an increase in intensity starting near ~700 K for partially metamict zircon, whereas for highly damaged zircon the first recovery of the feature takes place near 1000 K, accompanied by a decrease in the radiation-induced broad band. The changes observed in the present study reflect the variations of local environments of U ions in natural zircon during metamictization and thermal annealing.     

Thorium-uranium disequilibrium in a geothermal discharge zone at yellowstone

Whole rock samples of hydrothermally-altered Biscuit Basin rhyolite from Yellowstone drill cores Y-7 and Y-8 were analyzed for ²³⁰Th, ²³⁴U, ²³⁸U, and ²³²Th. Extreme disequilibrium was found, with (²³⁰Th/ ²³⁴U) ranging from 0.30 to 1.27. Values of (²³⁰Th/²³²Th) and (²³⁴U/²³²Th) define a linear correlation with a slope of 0.16 ± 0.01, which corresponds to a (²³⁰Th/²³⁴U) age of approximately 19 ka. The (²³⁰Th/²³⁴U) disequilibrium was apparently caused by U redistribution which occurred mostly at about 19 ka, and is not related simply to the relative degree of hydrothermal alteration and self-sealing of the rhyolite. Mass balance of U requires a large flux of U-bearing groundwater through the rhyolite at the time of U redistribution; rough estimates of minimum water/rock ratio range from 10² to 10⁴, for a range of possible groundwater U concentrations. Conservative hydraulic calculations indicate that the required groundwater flux could have occurred within a period of hundreds of years prior to self-sealing. The disequilibrium data are consistent with a model involving U redistribution during the initial stages of development of a geothermal discharge zone that formed in response to the hydrogeologic effects of glacial melting and unloading during the decline of the Pinedale Glaciation.     

Isotopic disequilibrium effects in leaching of natural uraninite and thorianitc

Fractional leach rates of ²²⁸Th that are greater than those of ²³²Th from natural uraninite and thorianite have been interpreted by Eyal and Fleischer in terms of α-decay damage to the crystal lattice. An alternative interpretation proposed here is that the enhanced leaching of ²²⁸Th is due to its presence as interstitial ions.     

Budgets and behaviors of uranium and thorium series isotopes in Santa Monica Basin sediments

Nine natural decay-series isotopes were measured in six box cores collected from a transect across the Santa Monica Basin. The ²¹⁰Pb-derived sedimentation rate decreases from ~80 mg/cm²-yr at the slope to ~20 mg/cm²-yr in the deep central basin. Sediment mixing prevails in sites underlying oxic waters, but is subdued in the anoxic deep basin below the sill depth. Uranium contents in sediments are controlled by levels of authigenic U, which are higher in the more reduced condition in the deep basin. Most of the authigenic U results from precipitation within the sediments.The ²³²Th-²²⁸Th disequilibrium in sediments indicates that ²²⁸Ra is lost from the sediments from a depth of ~ 10 cm upward. Modelling the distribution of excess ²²⁸Th and ²³⁴Th in the surficial layers of the deep basin sediments results in a mean sediment mixing coefficient of 0.2 cm²/yr and a sedimentation rate close to that based on ²¹⁰Pb. There is no evidence of changing sedimentation rate in the central basin during the past century. Fluxes of excess ²¹⁰Pb, ²³⁰Th and ²³¹Pa to the central Santa Monica Basin sediments are much higher than what can be predicted from local supply. Advective input of open ocean waters coupled with enhanced scavenging of these reactive nuclides at the ocean margin is considered to be the primary cause.     

Investigation of natural background radiation of sediments in Rameswaram Island,Tamil Nadu,India

The aim of the study is to assess the natural background radiation in and around Rameswaram Island. In this context, samples were collected to measure the gamma radiations of ²³⁸U, ²³²Th, and ⁴⁰K using NaI(Tl) detector-based gamma ray spectrometer. The average activity concentrations of ²³⁸U, ²³²Th, and ⁴⁰K are noted to be well below the world average values. The calculated absorbed dose rate, radium equivalent activity, and hazard index values were below the prescribed limit. The grain size of the sediment was analyzed following Trefethen’s nomenclature, and its correlation with the natural background radioactivity was studied. The sample that contained clay show elevated activity of ⁴⁰K. The percentage of heavy minerals shows concomitant variation in natural radioactivity, especially in the activity of ²³⁸U and ²³²Th.     

A U-series study of lavas from Kamchatka and the Aleutians: constraints on source composition and melting processes

New data are presented for lavas from the Kamchatka Peninsula and the Aleutian arc. Radiogenic isotopes are strikingly homogeneous in the Kamchatka lavas and although incompatible trace element ratios exhibit much greater variability, much of this appears to result from shallow level, crystal fractionation. The data reveal little systematic across-arc change in radiogenic isotopes or trace element ratios. The Nd and Pb isotope data overlap those for Pacific MORB and limit the amount of sediment that could be incorporated in the mantle source region to <1% which is insufficient to account for the observed La/Ta ratios (50–68) in the high-MgO lavas. The lack of a positive correlation between La/Ta and depth to the slab suggests that melt–wall rock interaction was not important in controlling this ratio. Instead it is inferred that La/Ta increased during partial melting and that D_La/D_Ta = 0.11–0.06, possibly due to residual amphibole. Ba, U, Sr and Pb were added to the source by an aqueous fluid from the subducting slab and its inferred isotopic composition indicates that this fluid was derived from the altered oceanic crust. The addition of U resulted in a large range of (²³⁸U/²³²Th) from 0.79–2.48 similar to that observed in the Mariana and Lesser Antilles island arcs. However, (²³⁰Th/²³²Th) = 0.79–2.34, and the majority of samples lie close to the equiline indicating that the time since U/Th fractionation is generally ≥150 thousand years. The large width of the volcanic zone is assumed to reflect protracted fluid release from the subducting slab over the depth interval 170–380 km possibly coupled with extension across the Central Kamchatka Depression. The data from the Aleutians contrast strongly with those from Kamchatka. Radiogenic isotope data indicate that the Aleutian lavas contain a significant recycled sedimentary component, consistent with elevated ¹⁰Be/⁹Be ratios. The Aleutian lavas have (²³⁰Th/²³²Th) = 0.79–2.34 and exhibit a significant range of U/Th disequilibria [(²³⁸U/²³⁰Th) = 0.75–1.01]. However, ¹⁰Be/⁹Be is positively correlated with (²³⁸U/²³⁰Th) suggesting that the ¹⁰Be signal was carried by the aqueous fluid from the slab. The U/Th disequilibria for the Aleutian lavas lie close to a 30 thousand year reference line suggesting that this fluid was released from the slab ∼30 thousand years ago similar to recent estimates from the Lesser Antilles, Marianas, and Tonga-Kermadec island arcs from which it is inferred that fluid addition was the trigger for partial melting. Given that the rate of convergence in Kamchatka is similar to that in the Aleutians, Marianas and Tonga-Kermadec the inferred greater time since␣fluid release in Kamchatka requires further investigation. Received: 24 September 1997 / Accepted: 7 July 1998     

The transport of U- and Th-series nuclides in sandy confined aquifers

Abundances of ²³⁸U, ²³⁴U, ²³²Th, ²²⁶Ra, ²²⁸Ra, ²²⁴Ra, and ²²²Rn were measured in groundwaters of the Ojo Alamo aquifer in northwest New Mexico. This is an arid area with annual precipitation of ∼22 cm. The purpose was to investigate the transport of U-Th series nuclides and their daughter products in an old, slow-moving groundwater mass as a means of understanding water-rock interactions and to compare the results with a temperate zone aquifer. It was found that ²³²Th is approximately at saturation and supports the view of Tricca et al. (2001) that Th is precipitated irreversibly upon weathering, leaving surface coatings of ²³²Th and ²³⁰Th on aquifer grains. Uranium in the aquifer waters has very high [²³⁴U/²³⁸U] ∼ 9 and low ²³⁸U concentrations. These levels can be explained by low weathering rates in the aquifer (w_238U ∼ 2 × 10⁻¹⁸ to 2 × 10⁻¹⁷s⁻¹) using a continuous flow, water-rock interaction model. The Ra isotopes are roughly in secular equilibrium despite their very different mean lifetimes. The ²²²Rn and ²²⁸Ra isotopes in the aquifer correspond to ∼10% of the net production rate of the bulk rock. This is interpreted to reflect an earlier formed irreversible surface coating of Th that provides Ra and Rn to the aquifer waters. The surface waters that appear to be feeding the aquifer have low [²³⁴U/²³⁸U] and high ²³⁸U concentrations. The flow model shows that it is not possible to obtain the high [²³⁴U/²³⁸U] and low [²³⁸U] values in the aquifer from a source like the present vadose zone input. It follows that the old aquifer waters studied cannot be fed by the present vadose zone input unless they are greatly diluted with waters with very low U concentrations. If the present sampling of vadose zone sources is representative of the present input, then this requires that there was a major change in water input with much larger rainfall some several thousand years ago. This may represent a climatic change in the Southwest.     

Distribution of 238U, 232Th and 40K in plutonic rocks of Greece

One hundred and twenty one samples from every major plutonic body (mainly granitic) of Greece have been analyzed by γ-ray spectrometry to determine the specific activities of ²³⁸U, ²³²Th and ⁴⁰K (Bq/kg). The range of the activity concentrations of these radionuclides was 2.3–266.4, 1.8–375.5 and 55.0–1632.0 Bq/kg and their average values were 79.2, 85.3 and 881.4 Bq/kg respectively. Any possible connection between the specific activities of ²³⁸U, ²³²Th and ⁴⁰K and some characteristics of the studied samples (age, rock-type, colour, grain-size, occurrence and chemical composition) is investigated. Samples of particular colour, rock-type, occurrence and chemical composition have been identified for their distinctive levels of natural radioactivity, while age and grain-size do not affect the concentrations of ²³⁸U, ²³²Th and ⁴⁰K. The range of the Th/U ratio was 0.7–12.69. This great variation in the Th/U ratios, especially when it is found among the samples of the same pluton, is also discussed and explained by alteration and tectonic–metamorphic processes.     

Redistribution of uranium and thorium series isotopes during isovolumetric weathering of granite

Previous studies of the distribution of U and Th in parent versus weathered granites have shown both depletion and enrichment of these elements during weathering. In this study, the distribution of U and Th decay series isotopes was determined in a weathering profile of a granitic saprolite, which showed textural preservation indicating isovolumetric weathering. Two types of dissolution methods were used: a whole-rock dissolution and a sodium-citrate dithionite leach to preferentially attack noncrystalline phases of weathering products. Using volume-based activities, 45–70 percent of the total ²³²Th was gradually removed during weathering. Although the whole-rock ${}^{228}\text{Th}{}^{232}\text{Th}$ activity ratios were in equilibrium, there were large excesses of ²²⁸Th in the leachable fraction of both parent rock (${}^{228}\text{Th}{}^{232}\text{Th}\text{= 2.06}$) and partially weathered saprolite (${}^{228}\text{Th}{}^{232}\text{Th}\text{= 3–6.5}$), due to alpha recoil and release of daughter ²²⁸Th to the weathering rind of the mineral grain. For the most weathered sample, 81 percent of the thorium was in the teachable fraction and ${}^{228}\text{Th}{}^{232}\text{Th}\text{= 1}$, indicating that even the more resistant minerals were attacked.The total U activities showed as much variation in the six parent rock samples as in the weathered profile, and ${}^{234}\text{U}{}^{238}\text{U}$ were in equilibrium in both the whole-rock and leachable fractions. ²³⁰Th was deficient relative to ²³⁴U and ²²⁶Ra in both fractions, suggesting recent addition of U and Ra to the entire profile. The large variation in U was not from absorption onto the intermediate weathering products, because only 11–23 percent of the U was in the leachable fraction.     

Transport of radionuclides in an unconfined chalk aquifer inferred from U-series disequilibria

U-series disequilibria measured in waters and rocks from a chalk aquifer in France have been used as an analog for long-term radionuclide migration. Drill core samples from a range of depths in the vadose zone and in the saturated zone, as well as groundwater samples were analyzed for ²³⁸U, ²³⁴U, ²³²Th and ²³⁰Th to determine transport mechanisms at the water/rock interface and to quantify parameters controlling the migration of radionuclides. Isotope measurements in rocks were done by TIMS, whereas (²³⁴U/²³⁸U) and (²³⁰Th/²³²Th) activity ratios in water samples were measured by multi-collector-ICP-MS. Both depletion and enrichment in ²³⁴U relative to ²³⁸U were observed in carbonate rock samples resulting from chemical weathering in the unsaturated zone and calcite precipitation in the zone of water-table oscillation, respectively. The correlation between (²³⁰Th/²³²Th) activity ratios and ⁸⁷Sr/⁸⁶Sr ratios found in the chalk samples indicates that thorium is mainly contained in a minor silicate phase whose abundance is variable in chalk samples. Water samples are all characterized by (²³⁴U/²³⁸U) > 1 resulting from α-recoil effect of ²³⁴Th. Groundwaters are characterized by a more radiogenic signature in ⁸⁷Sr/⁸⁶Sr than the rocks. Moreover, (²³⁰Th/²³²Th) activity ratios in the waters are lower than in the rocks, and increase with distance from the water divide, which suggests that Th transport is controlled by colloids formed during water infiltration in the soil. A 1-D transport model has been developed in order to constrain the U-series nuclide transport considering a transient behavior of radionuclides in the aquifer and a time-dependent composition for the solid phase. This model permits a prediction of the time scale of equilibration of the system, and an estimation of parameters such as weathering rate, distribution coefficients and α-recoil fractions. Retardation factors of 10-35 and from 1 × 10⁴ to 2 × 10⁵ were predicted for U and Th, respectively, and can be used to predict the migration of radionuclides released as contaminants in the environment. At the scale of our watershed (∼32 km²), a characteristic migration time from recharge to riverine discharge of 200-600 yr for U and 0.2-3.7 Myr for Th was obtained.     

Tracing the metasomatic and magmatic evolution of continental mantle roots with Sr, Nd, Hf and and Pb isotopes: A case study of Middle Atlas (Morocco) peridotite xenoliths

We studied clinopyroxenes from spinel-facies peridotite xenoliths sampled by the Quaternary intra-plate volcanism of the Middle Atlas (Morocco) and present new trace element and Sr-Nd-Hf isotope data. However, we focus in particular on Pb isotope data and ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb ratios of these clinopyroxenes. This data allows us to investigate: (a) the timing of metasomatic events, (b) the prevalence and persistence of elevated ²³⁸U/²⁰⁴Pb, ²³²Th/²³⁸U and ²³²Th/²⁰⁴Pb in continental mantle roots and (c) the ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb composition of putative basaltic melts generated from such metasomatised sub-continental lithospheric mantle (SCLM).Incompatible trace element concentrations in these clinopyroxenes are elevated, marked by high-field strength element depletion and fractionated elemental ratios (e.g., U/Nb, Zr/Hf) most consistent with enrichment due to carbonatitic liquids. Sr, Nd and Hf isotopes have an affinity to HIMU.U, Th and Pb abundances in the clinopyroxenes generally exceed estimates of primitive mantle clinopyroxene. Pb isotope compositions of these clinopyroxenes are radiogenic and vary between ²⁰⁶Pb/²⁰⁴Pb = 19.93-20.25, ²⁰⁷Pb/²⁰⁴Pb = 15.63-15.66 and ²⁰⁸Pb/²⁰⁴Pb = 39.72-40.23. These Pb isotope systematics result in generally negative Δ7/4 but positive Δ8/4; setting these samples distinctly apart from typical HIMU. These Pb isotope compositions are also distinct from the associated host volcanic rocks. ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb of these clinopyroxenes, which range from 26 to 81 and 136 to 399, respectively, are elevated and more extreme than estimates of MORB- and HIMU-source mantle.The Pb isotope evolution of the clinopyroxenes suggests that the metasomatic enrichment is younger than 200 Ma, which discounts the volcanic activity due to the opening of the Atlantic and the onset of the collision of the African and Eurasian plates as processes generating the lithophile element and isotope composition of this continental mantle root. Instead, the enrichment is thought to be associated with the Quaternary intra-plate volcanism in the Middle Atlas. However, the erupted mafic melts have unradiogenic Pb isotopes and lower ²³⁸U/²⁰⁴Pb, ²³²Th/²⁰⁴Pb and ²³²Th/²³⁸U relative to the clinopyroxene and do not seem to have equilibrated with the clinopyroxenes. The high Th abundances and the high ²³²Th/²³⁸U also suggest that the metasomatism was due to carbonatitic liquids.When literature data for Pb isotopes in mantle minerals are considered, the Pb isotope range of Archean, Proterozoic and Phanerozoic continental mantle roots is remarkable in that they are similar to the convecting mantle. This observation does not support the existence of sub-continental lithospheric mantle with high ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb for long periods of time. Consequently, the narrow range of Pb isotopes in SCLM worldwide suggests that only the youngest metasomatic events are recorded by incompatible elements such as U, Th and Pb. Numerical modelling of putative magmas generated from Middle Atlas SCLM by fractional, non-modal melting calculations yield extremely high ²³⁸U/²⁰⁴Pb and ²³²Th/²⁰⁴Pb ratios. For example, pure SCLM magmas generated from 0.5% to 10% melting are anticipated to have ²³²Th/²⁰⁴Pb ratios exceeding those known from terrestrial basalts.     

Dating fluvial terraces by Th/U on pedogenic carbonate, Wind River Basin, Wyoming

Reliable and precise ages of Quaternary pedogenic carbonate can be obtained with ²³⁰Th/U dating by thermal ionization mass spectrometry applied to carefully selected milligram-size samples. Datable carbonate can form within a few thousand years of surface stabilization allowing ages of Quaternary deposits and surfaces to be closely estimated. Pedogenic carbonate clast-rinds from gravels of glacio-fluvial terraces in the Wind River Basin have median concentrations of 14 ppm U and 0.07 ppm ²³²Th, with median (²³⁰Th/²³²Th) = 270, making them well suited for ²³⁰Th/U dating. Horizons as thin as 0.5 mm were sampled from polished slabs to reduce averaging of long (≥10⁵ yr), and sometimes visibly discontinuous, depositional histories. Dense, translucent samples with finite ²³⁰Th/U ages preserve within-rind stratigraphic order in all cases. Ages for terraces WR4 (167,000 ± 6,400 yr) and WR2 (55,000 ± 8600 yr) indicate a mean incision rate of 0.26 ± 0.05 m per thousand years for the Wind River over the past glacial cycle, slower than inferred from cosmogenic-nuclide dating. Terrace WR3, which formed penecontemporaneously with the final maximum glacial advance of the penultimate Rocky Mountain (Bull Lake) glaciation, has an age of 150,000 ± 8300 yr indicating that it is broadly synchronous with the penultimate global ice volume maximum.     

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.     

铀系国际标准样鉴定结果讨论

铀系国际标准样的鉴定是开展铀系方法的一项基础工作。其主要内容是测定实验流程中所必需使用示踪剂的参数,测试地质样品中各项同位素比值和年龄,检验各国铀系实验室的全部实验程序。     

Assessment of natural radioactivity,associated radiological health hazards indices and soil-to-crop transfer factors in cultivated area around a fertilizer factory in Onne,Nigeria

Concentration of natural radionuclides in three major staple food crops cultivated around a fertilizer plant in Onne, Rivers State Nigeria and the cultivated soil samples were determined using gamma spectroscopy operated on a Canberra vertical high purity 3″ × 3″ NaI(TI) detector. The average activity concentration of ²³⁸U, ²³²Th and ⁴⁰K was determined, for cassava flour (U 19.3 ± 5.0, Th 11.4 ± 3.3, K 426.9 ± 33.8) Bq kg^?1, for yam flour (U 6.3 ± 1.8, Th 8.4 ± 2.6, K 227.0.9 ± 27.3) Bq kg^?1 while for cocoyam flour (U 7.5 ± 2.7, Th 7.1 ± 2.3, K 195.8 ± 25.83) Bq kg^?1. The mean activity concentration for soil samples is 18.7 ± 3.7 Bq kg^?1, 18.0 ± 3.8 Bq kg^?1 and 308.4 ± 22.4 Bq kg^?1 for ²³⁸U, ²³²Th and ⁴⁰K, respectively. These values obtained show enhanced ⁴⁰K concentration which is attributed to the effluent discharge from a fertilizer plant and its applications to farmlands, but ²³⁸U, ²³²Th values are well within the global average and values reported in some regions and countries of the world. Radiation hazard indices obtained to estimate potential radiological health risk in both foodstuffs and soil samples are well below their permissible limit as set by UNSCEAR [Sources and effects of ionizing radiation (Report to the General Assembly), 2000]. The rate of radionuclides transfer from soil to crops was moderate with mean transfer factors of ²³²Th < ²³⁸U < ⁴⁰K.     

New Thorium Isotope Ratio Measurements in Silicate Reference Materials: A‐THO,AGV‐2, BCR‐2, BE‐N,BHVO‐2 and BIR‐1

A two‐step Th isolation protocol, involving micro‐columns of TRU‐Spec extraction chromatography material and AG1 resin, was evaluated. The MC‐ICP‐MS procedure included ²³²Th tailing characterisation and correction, and calibrator bracketing using an in‐house standard solution (ThS1) to correct for instrumental mass bias and Faraday cup to secondary electron multiplier relative gain. Repeated analyses of reference solutions (UCSC Th ‘A’, WUN, OU Th ‘U’, IRMM‐36) were consistent with published data. Six reference materials (A‐THO, BCR‐2, AGV‐2, BHVO‐2, BE‐N and BIR‐1) were processed. The average ²³⁰Th/²³²Th values obtained for these samples are in excellent agreement with published data. In addition, we report the first ²³⁰Th/²³²Th values for BE‐N and BIR‐1. The intermediate precisions for rock samples ranged from ± 0.24 to ± 0.49% (2 RSD) and were similar to those achieved for synthetic solutions, thereby supporting the overall validity of the chemical separation, data acquisition and reduction procedures. Counting statistics on the ²³⁰Th isotope was the most significant source of uncertainty. The intermediate precision of the mean ²³⁰Th/²³²Th for the Th‐depleted BIR‐1 (5.64 × 10^?6 ± 0.27%, 2 RSD) is in the range of the analyses of other reference materials analysed in this study.     

U-Th chronology and paleoceanographic record in a Fe-Mn crust from the NE Atlantic over the last 700 ka

Hydrogenetic ferromanganese crusts (Fe-Mn crusts) provide a secular record of the variations of seawater composition responding to changes in ocean circulation and erosion processes. In this respect, the acquisition of an absolute and reliable chronology in Fe-Mn crusts is a prerequisite. Here we combine four different and complementary chronometers (¹⁰Be, ²³⁰Th_ex, ²³⁰Th_ex/²³²Th, ²³⁴U/²³⁸U) in a Fe-Mn crust dredged at ∼2000 m depth in the east Atlantic to first establish a reliable chronology over the Quaternary period. Then, we use EDS chemical analysis to look for correlation between major element chemistry and climate changes. (²³⁰Th_ex), (²³⁰Th_ex/²³²Th), and Be data give very consistent growth rates. In particular, the good match between (²³⁰Th_ex) and (²³⁰Th_ex/²³²Th) data indicates that at the location of crust 121DK, ²³⁰Th and ²³²Th fluxes in the water column change simultaneously and suggests that the normalization of ²³⁰Th_ex to ²³²Th makes (²³⁰Th_ex/²³²Th) a better chronometer. Our best-fit model suggests that crust 121DK experienced changes in growth rates at ∼122 and 312 ka and a growth with a constant ²³⁰Th initial flux. This chronology returns an age of 680 ka for the uppermost 1.5 mm. The (²³⁴U/²³⁸U) depth profile, however, was clearly affected by diffusion of ²³⁴U in the porous crust and can therefore not be used to derive a reliable chronology. One part of the crust seems isolated from pore water diffusion and can be physically recognized as a zone of very small porosity. On the basis of the (²³⁰Th_ex/²³²Th) chronology, major element chemistry is shown to be linked to climate change. Mn/Fe variations compare well with those in a Fe-Mn crust from the Pacific, showing systematic maxima during glacial stages 2 and 4. High Mn/Fe are tentatively interpreted to reflect expansion of the oxygen minimum zone during glacial periods, resulting from higher bioproductivity. In addition we note that the surface (²³⁰Th/²³²Th) activity ratio of crust 121DK is entirely consistent with advection of deep water from the western toward the eastern Atlantic basin.     

Geochemical evolution of a shallow magma plumbing system during the last 500 years, Miyakejima volcano, Japan: Constraints from U-Th-Ra systematics

In order to unravel magma processes and the geochemical evolution of shallow plumbing systems beneath active volcanoes, we investigated U-series disequilibria of rocks erupted over the past 500 years (1469-2000 AD) from Miyakejima volcano, Izu arc, Japan. Miyakejima volcanic rocks show ²³⁸U-²³⁰Th-²²⁶Ra disequilibria with excess ²³⁸U and ²²⁶Ra, due to the addition of slab-derived fluids to the mantle wedge. Basaltic bombs of the 2000 AD eruption have the lowest (²³⁰Th/²³²Th) ratio compared to older Miyakejima eruptives, yielding the youngest ²³⁸U-²³⁰Th model age of 2 kyr. This reinforces our previous model that fluid release from the slab and subsequent magma generation in the mantle wedge beneath Miyakejima occur episodically on a several-kyr timescale. In the last 500 years, Miyakejima eruptives show: (1) a vertical trend in a (²³⁰Th/²³²Th)-(²³⁸U/²³²Th) diagram and (2) a positive linear correlation in a (²²⁶Ra/²³⁰Th)₀ − 1/²³⁰Th diagram, which is also observed in lavas from some of the single eruptions (e.g., 1940, 1962, and 1983 AD). The variations cannot be produced by simple fractional crystallization in a magma chamber with radioactive decay of ²³⁰Th and ²²⁶Ra, but it is possibly produced by synchronous generation of melts in the mantle wedge with different upwelling rate or addition of multiple slab-derived fluids. A much more favorable scenario is that some basaltic magmas were intermittently supplied from deep in the mantle and injected into the crust, subsequently modifying the original magma composition and producing variations in (²³⁰Th/²³²Th) and (²²⁶Ra/²³⁰Th)₀ ratios via assimilation and fractional crystallization (AFC). The assimilant of the AFC process would be a volcanic edifice of previous Miyakejima magmatism. Due to the relatively short timescales involved, the interaction between the assimilant and recent Miyakejima magmatism has not been recorded by the Sr-Nd-Pb isotopic systems. In such cases, Th isotopes and (²²⁶Ra/²³⁰Th) ratio are excellent geochemical tracers of magmatic evolution.     

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.     

青岛市天然放射性环境地质调查

对青岛地区进行了大规模的天然放射性环境地质调查和评价中发现,青岛地区陆地伽马辐射剂量率虽然略高于全国和山东省的平均水平,但仍属于天然辐射安全区域.测区的伽马辐射剂量率值总体上决定于岩性.伽马辐射剂量率都来自于²³⁸U、²³²Th、⁴⁰K的贡献,但是与其他地区不同,⁴⁰K和²³²Th对剂量率的贡献要大于²³⁸U.此外,一些公路、建筑等建造材料中的放射性核素的含量直接影响着这些工程的放射剂量,主要是在建造这些工程时所选用的石材、石料和水泥等,都会对当地的放射剂量有着重大的影响.