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1.
Deep-sea coral has proved useful for paleoceanographic reconstructions and for documenting 14C-ages of water masses using 230Th-ages. However, for precise and accurate U-series dating, further information on coral-age structure, growth rate and diagenetic evolution is still needed. To document such processes, we used U-Th-226Ra systematics in a 40 cm diameter, Lophelia pertusa specimen collected in 1912 from the Eastern Atlantic (Sea of the Hebrides). External parts of the specimen are thought to have been alive when collected whereas more internal parts were likely dead. The “live-collected” and “dead” parts of the skeleton were sampled and analyzed for their 230Th, 232Th, 234U, 238U, 226Ra and Ba contents by thermal ionization and multicollector inductively coupled plasma mass spectrometry. 230Th/234U ratios in the most recent parts yielded ages of 86 ± 6 a and 92 ± 9 a, in agreement with the date of recovery. The older parts yielded 230Th ages ranging from 169 ± 15 to 211 ± 10 a (n = 5), but had a 31% higher U content than more recent parts of the skeleton. This raises concerns about the possibility of secondary diagenetic U uptake, although an environmentally controlled U/Ca shift between coral growth stages cannot be ruled out. 226Ra/Ba measurements were made, and model- 226Ra/Ba ages averaging 250 ± 12 yr were calculated for the older part, assuming a constant initial 226Ra/Ba ratio in bottom waters. These ages are slightly older than 230Th-ages, suggesting either that 226Ra/Ba ratios of ambient-seawater changed over time or that a diagenetic phenomenon have affected the U-series system, or both. Scanning electron microscope observations revealed bioerosion and secondary biomineralization in the older part of the coral skeleton, supporting the hypothesis that diagenetic processes may have influenced the ages obtained by the U-series toolbox. Modeled U-series ages for such an open system are discussed. However, a comparison between 14C- and 230Th-ages performed on both pristine and bioeroded parts of the coral gives coherent values (ca 450 a) for the preindustrial 14C-reservoir age of North Atlantic waters. It remains to be determined, however, whether diagenesis occurs rapidly over a short period of time, or whether it continues for longer periods. In the latter case, diagenetic processes would hamper paleoceanographic interpretations as well as the precise calculation of 14C ages of deep-water masses, based on comparative U/Th- and 14C-chronologies.  相似文献   

2.
Although most arc lavas have experienced significant magma differentiation, the effect of the differentiation process on U-series disequilibria is still poorly understood. Here we present a numerical model for simulating the effect of time-dependent magma differentiation processes on U-series disequilibria in lavas from convergent margins. Our model shows that, in a closed system with fractional crystallization, the ageing effect can decrease U-series disequilibria via radioactive decay while in an open system, both ageing and bulk assimilation of old crustal material serve to reduce the primary U-series disequilibria. In contrast, with recharge of refresh magma, significant 226Ra excess in erupted lavas can be maintained even if the average residence time is longer than 8000 years.The positive correlations of (226Ra/230Th) between Sr/Th or Ba/Th in young lavas from convergent margins have been widely used as evidence of fluid addition generating the observed 226Ra excess in subduction zones. We assess to what extent the positive correlations of (226Ra/230Th) with Sr/Th and Ba/Th observed in the Tonga arc could reflect AFC process. Results of our model show that these positive correlations can be produced during time-dependent magma differentiation at shallow crustal levels. Specifically, fractional crystallization of plagioclase and amphibole coupled with contemporaneous decay of 226Ra can produce positive correlations between (226Ra/230Th) and Sr/Th or Ba/Th (to a lesser extent). Therefore, the correlations of (226Ra/230Th) with Sr/Th and Ba/Th cannot be used to unambiguously support the fluid addition model, and the strength of previous conclusions regarding recent fluid addition and ultra-fast ascent rates of arc magmas is significantly lessened.  相似文献   

3.
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.226Raex/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 226Raex/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 226Raex/226Ra(0) ages agreed well with those derived from 230Th/234U, (ii) all data plot within uncertainty on the 226Raex/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, 226Raex/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.  相似文献   

4.
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.  相似文献   

5.
The development of U-series nuclides for investigating weathering processes has been significantly stimulated by the analytical improvement made over the last decades in measuring the 238U series with intermediate half-lives (i.e., 234U–230Th–226Ra). It is proposed in this paper to present principles and methods that are now being developed to determine weathering rates from the study of U-series nuclides in soils and weathering profiles. Mathematical approaches, developed to calculate such rates, are based on some implicit assumptions that are also presented and must be kept in mind if one wants to correctly interpret the obtained ages.  相似文献   

6.
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 DU and DU/DTh, 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.  相似文献   

7.
U-series radioactive disequilibria in basaltic lavas have been used to infer many important aspects of melt generation and extraction processes in Earth’s mantle and crust, including the porosity of the melting zone, the solid mantle upwelling rate, and the melt transport rate. Most of these inferences have been based on simplified theoretical treatments of the fractionation process, which assume equilibrium partitioning of U-series nuclides among minerals and melt. We have developed a numerical model in which solid-state diffusion controls the exchange of U-series nuclides among multiple minerals and melt. First the initial steady-state distribution of nuclides among the phases, which represents a balance between diffusive fluxes and radioactive production and decay, is calculated. Next, partial melting begins, or a foreign melt is introduced into the system, and nuclides are again redistributed among the phases via diffusion. U-series nuclides can be separated during this stage due to differences in their diffusivity; radium in particular, and possibly protactinium as well, can be strongly fractionated from slower-diffusing thorium and uranium. We show that two distinct processes are not required for the generation of 226Ra and 230Th excesses in mid-ocean ridge basalts, as has been argued previously; instead the observed negative correlations of the (226Ra/230Th) activity ratio with (230Th/238U) and with the extent of trace element enrichment may result from diffusive fractionation of Ra from Th during partial melting of the mantle. Alternatively, the (226Ra/230Th) disequilibrium in mid-ocean ridge basalts may result from diffusive fractionation during shallow-level interaction of mantle melts with gabbroic cumulates, and we show that the results of the interaction have a weak dependence on the age of the cumulate if both plagioclase and clinopyroxene are present.  相似文献   

8.
采用氢氟酸-硝酸-盐酸混合酸密闭消解含铀矿石样品,用阴离子交换树脂、阳离子交换树脂和锶特效树脂逐级分离富集铀、钍和镭。使用高分辨电感耦合等离子体质谱(HR-ICPMS)测定分离纯化液中234U/238U2、30Th/232Th和228Ra/226Ra同位素。比值的测量精密度取决于比值的大小和对应核素浓度的大小。对质量浓度为10 ng/mL天然铀测量液,234U/238U的测量精密度优于1.2%;对230Th质量浓度为0.6ng/mL且230Th和232Th质量浓度接近的测量液,230Th/232Th的测量精密度为1.2%;对228Ra质量浓度为0.48 pg/mL且228Ra和226Ra质量浓度接近的测量液,228Ra/226Ra的测量精密度为4.0%。  相似文献   

9.
Factors controlling the groundwater transport of U, Th, Ra, and Rn   总被引：1，自引：0，他引：1  
A model for the groundwater transport of naturally occurring U, Th, Ra, and Rn nuclides in the238U and232Th decay series is discussed. The model developed here takes into account transport by advection and the physico-chemical processes of weathering, decay, α-recoil, and sorption at the water-rock interface. It describes the evolution along a flowline of the activities of the238U and232Th decay series nuclides in groundwater. Simple sets of relationships governing the activities of the various species in solution are derived, and these can be used both to calculate effective retardation factors and to interpret groundwater data. For the activities of each nuclide, a general solution to the transport equation has been obtained, which shows that the activities reach a constant value after a distance ϰi, characteristic of each nuclide. Where ϰi is much longer than the aquifer length, (for238U,234U, and232Th), the activities grow linearly with distance. Where gKi is short compared to the aquifer length, (for234Th,230Th,228Th,228Ra, and224Ra), the activities rapidly reach a constant or quasi-constant activity value. For226Ra and222Rn, the limiting activity is reached after 1 km. High δ234U values (proportional to the ratioɛ234Th/W238U) can be obtained through high recoil fraction and/or low weathering rates. The activity ratios230Th/232Th,228Ra/226Ra and224Ra/226Ra have been considered in the cases where either weathering or recoil is the predominant process of input from the mineral grain. Typical values for weathering rates and recoil fractions for a sandy aquifer indicate that recoil is the dominant process for Th isotopic ratios in the water. Measured data for Ra isotope activity ratios indicate that recoil is the process generally controlling the Ra isotopic composition in water. Higher isotopic ratios can be explained by different desorption kinetics of Ra. However, the model does not provide an explanation for228Ra/226Ra and224Ra/226Ra activity ratios less than unity. From the model, the highest222Rn emanation equals 2ɛ. This is in agreement with the hypothesis that222Rn activity can be used as a first approximation for input by recoil (Krishnaswamiet al 1982). However, high222Rn emanation cannot be explained by production from the surface layer as formulated in the model. Other possibilities involve models including surface precipitation, where the surface layer is not in steady-state.  相似文献   

10.
We present data for U and its decay series nuclides 230Th, 226Ra, 231Pa, and 210Po for 14 lavas from Kick’em Jenny (KEJ) submarine volcano to constrain the time-scales and processes of magmatism in the Southern Lesser Antilles, the arc having the globally lowest plate convergence rate. Although these samples are thought to have been erupted in the last century, most have (226Ra)/(210Po) within ±15% of unity. Ten out of 14 samples have significant 226Ra excesses over 230Th, with (226Ra)/(230Th) up to 2.97, while four samples are in 226Ra-230Th equilibrium within error. All KEJ samples have high (231Pa)/(235U), ranging from 1.56 to 2.64 and high 238U excesses (up to 43%), providing a global end-member of high 238U and high 231Pa excesses. Negative correlations between Sr, sensitive to plagioclase fractionation, and Ho/Sm, sensitive to amphibole fractionation, or K/Rb, sensitive to open system behavior, indicate that differentiation at KEJ lavas was dominated by amphibole fractionation and open-system assimilation. While (231Pa)/(235U) does not correlate with differentiation indices such as Ho/Sm, (230Th)/(238U) shows a slight negative correlation, likely due to assimilation of materials with slightly higher (230Th)/(238U). Samples with 226Ra excess have higher Sr/Th and Ba/Th than those in 226Ra-230Th equilibrium, forming rough positive correlations of (226Ra)/(230Th) with Sr/Th and Ba/Th similar to those observed in many arc settings. We interpret these correlations to reflect a time-dependent magma differentiation process at shallow crustal levels and not the process of recent fluid addition at the slab-wedge interface.The high 231Pa excesses require an in-growth melting process operating at low melting rates and small residual porosity; such a model will also produce significant 238U-230Th and 226Ra-230Th disequilibrium in erupted lavas, meaning that signatures of recent fluid addition from the slab are unlikely to be preserved in KEJ lavas. We instead propose that most of the 238U-230Th, 226Ra-230Th, and 235U-231Pa disequilibria in erupted KEJ lavas reflect the in-growth melting process in the mantle wedge (reflecting variations in U/Th, daughter-parent ratios, fO2, and thermal structure), followed by modification by magma differentiation at crustal depths. Such a conclusion reconciles the different temporal implications from different U-series parent-daughter pairs and relaxes the time constraint on mass transfer from slab to eruption occurring in less than a few thousand years imposed by models whereby 226Ra excess is derived from the slab.  相似文献   

11.
研究了TIMS测定铀矿石样品中234U/238U、230Th/232Th、228Ra/226Ra的方法。建立了铀矿石密闭混酸一次溶样的方法和采用阴离子、阳离子和Sr特效树脂逐级离子交换分离纯化U、Th和Ra的流程,满足了TIMS测量要求。测定结果表明：100～1000 ng的天然铀中234U/238U,其测量精密度从静态多接收的2.34%提高到动态多接收的0.47%;对230Th与232Th丰度接近、质量为1μg左右的钍,采用三带点样技术和法拉第多接收技术测定230Th/232Th,其内精度平均值为0.0048%,外精度为0.028%;采用单带加钽发射剂,ETP跳峰测定50～100 fg镭-228稀释剂中的228Ra/226Ra,其内精度小于0.10%,外精度小于0.20%。比较TIMS和HR-ICP-MS、α能谱法测定234U/238U、230Th/232Th、228Ra/226Ra结果,三者结果相吻合。TIMS测量法样品用量少、快速、准确、精密度高,是U、Th、Ra同位素比值测定方法的又一补充。  相似文献   

12.
The extent to which U-series disequilibria can be produced during partial melting of mafic lower crust is quantified using a simple batch melting model and both experimental and theoretical partition coefficients for U, Th and Ra. We show that partial melting of mafic lower crust can only produce small disequilibria between 238U, 230Th and 226Ra. Crystallisation of basalt and mixing between young basalt and crustal derived melts will have a similar or smaller effect. Consequently, U-series disequilibrium in arc andesites and dacites can generally only be an inherited feature derived from a mantle parent, unless the timescales of silicic magma production within the crust are short compared to the half-life of 226Ra. Our results have profound implications for several recent models of silicic magma production by thermal incubation and partial melting of the lower crust. We show that the 226Ra excess observed in most arc andesites and dacites requires extremely rapid differentiation and/or the involvement of mantle derived basalts less than a few thousand years old. Application to Mount St. Helens suggests that crystallisation of young mantle-derived magma is likely to be the dominant process in the formation of these dacites.  相似文献   

13.
Interpretation of U-series disequilibria in midocean ridge basalts is highly dependent on the bulk partition coefficients for U and Th and therefore the mineralogy of the mantle source. Distinguishing between the effect of melting processes and variable source compositions on measured disequilibria (238U-230Th-226Ra and 235U-231Pa) requires measurement of the radiogenic isotopes Hf, Nd, Sr, and Pb. Here, we report measurements of 238U-230Th-226Ra and 235U-231Pa disequilibria; Hf, Nd, Sr, and Pb isotopic; and major and trace element compositions for a suite of 20 young midocean ridge basalts from the East Pacific Rise axis between 9°28′ and 9°52′N. All of the samples were collected within the axial summit trough using the submersible Alvin. The geological setting and observational data collected during sampling operations indicate that all the rocks are likely to have been erupted from 1991 to 1992 or within a few decades of that time. In these samples, 230Th excesses and 226Ra excesses are variable and inversely correlated. Because the eruption ages of the samples are much less than the half-life of 226Ra, this inverse correlation between 230Th and 226Ra excesses can be considered a primary feature of these lavas. For the lava suite analyzed in this study, 226Ra and 230Th excesses also vary with lava composition: 226Ra excesses are negatively correlated with Na8 and La/Yb and positively correlated with Mg#. Conversely, 230Th excesses are positively correlated with Na8 and La/Yb and negatively correlated with Mg#. Th/U, 230Th/232Th, and 230Th excesses are also variable and correlated to one another. 231Pa excesses are large but relatively constant and independent of Mg#, La/Yb, Th/U, and Na8. The isotope ratios 143Nd/144Nd, 176Hf/177Hf, 87Sr/86Sr, and 208Pb/206Pb are constant within analytical uncertainty, indicating that they were derived from a common source. The source is homogeneous with respect to parent/daughter ratios Lu/Hf, Sm/Nd, Rb/Sr, and Th/U; therefore, the measured variations of Th/U, 230Th, and 226Ra excesses and major and trace element compositions in these samples are best explained by polybaric melting of a homogeneous source, not by mixing of compositionally distinct sources.  相似文献   

14.
Magmas erupted at mid-ocean ridges (MORB) result from decompression melting of upwelling mantle. However, the mechanism of melt transport from the source region to the surface is poorly understood. It is debated whether melt is transported through melt-filled conduits or cracks on short time scales (<∼ 103 yrs), or whether there is a significant component of slow, equilibrium porous flow on much longer time scales (>∼ 103-104 yrs). Radiogenic excess 226Ra in MORB indicates that melt is transported from the melting region on time scales less than the half life of 226Ra (∼1600 yrs), and has been used to argue for fast melt transport from the base of the melting column. However, excess 226Ra can be generated at the bottom of the melt column, during the onset of melting, and at the top of the melt column by reactive porous flow. Determining the depth at which 226Ra is generated is critical to interpreting the rate and mechanism of magma migration. A recent compilation of high quality U-series isotope data show that in many young basalts, 226Ra excess in MORB is negatively correlated with 230Th excess. The data suggest that 226Ra excess is generated independently of 230Th excess, and cannot be explained by “dynamic” or fractional melting, where observed radiogenic excesses are all generated at the base of the melt column. One explanation is that the negative correlation of activity ratios is a result of mixing of slow moving melt that has travelled through reactive, low-porosity pathways and relatively fast moving melt that has been transported in unreactive high-porosity channels. We investigate this possibility by calculating U-series disequilibria in a melting column in which high-porosity, unreactive channels form within a low-porosity matrix that is undergoing melting. The results show that the negative correlation of 226Ra and 230Th excesses observed in MORB can be produced if ∼60% of the total melt flux travels through the low-porosity matrix. This melt maintains 226Ra excesses via chromatographic fractionation of Ra and Th during equilibrium transport. Melt that travels through the unreactive, high-porosity channels is not able to maintain significant 226Ra excesses because Ra and Th are not fractionated from each other during transport and the transport time for melt in the channels to reach the top of the melt column is longer than the time scale for 226Ra excesses to decay. Mixing of melt from the high porosity channels with melt from the low-porosity matrix at the top of the melting column can produce a negative correlation of 226Ra and 230Th excesses with the slope and magnitude observed in MORB. This transport process can also account for other aspects of the geochemistry of MORB, such as correlations between La/Yb, αSm/Nd, and Th/U and 226Ra and 230Th excess.  相似文献   

15.
洞穴地点骨化石铀系年龄可信度的讨论*   总被引：2，自引：1，他引：1  
沈冠军 《第四纪研究》2007,27(4):539-545
骨化石是铀不平衡系测年法广泛应用而又颇有争议的研究对象。文章通过对典型铀加入模式的计算,指出以α能谱的精度,二种铀系年龄差异的显著性表明近期内有较大量铀的迁移,但其在误差范围内的一致不能保证样品构成封闭体系。以往积累的数据表明,大多数洞穴地点骨化石给出了二法一致的铀系年龄,但钙板与下伏骨化石铀系年龄大多差异显著且与地层顺序矛盾,即使被次生碳酸盐岩包裹,多半骨化石的铀系年龄仍显著偏低于其包裹体。此外,相当一部分样品的U-Th同位素比难以用简单的铀后期加入或淋失来解释。基于对次生碳酸盐岩铀系年龄可信度的认识,骨化石总体上不构成封闭体系,所载铀系年代信息只具有限的分辨率。  相似文献   

16.
U-series disequilibria are presented for Holocene samples from the Canary Islands and interpreted with special emphasis on the separate roles of plume vs. lithospheric melting processes. We report Th and U concentrations and (238U)/(232Th), (230Th)/(232Th), (230Th)/(238U) and (234U)/(238U) for 43 samples, most of which are minimally differentiated, along with (226Ra)/(230Th) and (231Pa)/(235U) for a subset of these samples, measured by thermal ionization mass spectrometry (TIMS). Th and U concentrations range between 2 and 20 ppm and 0.5 and 6 ppm, respectively. Initial (230Th)/(238U) ranges from 1.1 to 1.6. (226Ra)/(230Th)o ranges between 0.9 and 1.8 while (231Pa)/(235U)o ranges between 1.0 and 2.0.Our interpretation of results is based on a three-fold division of samples as a function of incompatible element ratio, such as Nb/U. The majority of samples have Nb/U = 47 ± 10, similar to most MORB and OIB. Higher ratios are found exclusively in alkali basalts and tholeiites from the eastern Canary Islands whereas lower ratios are exclusively found in differentiated rocks from the western Canary Islands. Those with ordinary Nb/U ratios are attributed to melting within the slowly ascending HIMU-dominated Canary plume.Higher Nb/U, generally found in more silica rich basalts from the eastern islands, is attributed to lithospheric contamination. Based on their trace element characteristics, two possible contaminants are amphibole veins (± other minerals) crystallized in the mantle from previous plume-derived basanite or re-melted plume-derived intrusive rocks. The high Nb/U signature of these materials is imparted on a melt of the lithosphere created either by the diffusive infiltration of alkalis or by direct reaction between basanites and peridotite. Mixing between plume-derived basanite and lithospheric melt accounts for the U-series systematics of most eastern island magmas including the well-known Timanfaya eruption. Lower Nb/U ratios in differentiated rocks from the western islands are attributed to fractional crystallization of amphibole ± phlogopite ± sphene from basanite during its ascent through the lithosphere. Based on changes in disequilibria, phonolites and tephrites are interpreted to result from rapid differentiation of primitive parents within millennia.  相似文献   

17.
《Applied Geochemistry》2003,18(1):127-134
Based on U-series disequilibrium arguments there is good evidence for the presence of U-rich accessory minerals in the outer mantle. The very large excesses of 226Ra and 231Pa activity relative to 230Th, 238U, and 235U in most mid-ocean ridge basalts and some non-divergent plate-margin basalts are inconsistent with prevailing incompatibility models of U-series fractionation. Application of a fundamental principle of equilibrium balance reveals that in these instances more than half of the original U and Th remains behind in the residual outer mantle when basaltic magmas separate. One is forced to conclude that, in the outer mantle, U and Th do not occur primarily in major silicate minerals, where they would indeed be incompatible. Rather, they must be occurring as high concentration components in refractory accessory minerals. The precipitous concentration gradients bounding such minerals would allow for the operation of physical processes, such as alpha recoil and daughter diffusion, to produce paired disequilibrated phases. Daughter deficiencies would develop in the high concentration minerals, and daughter excesses in the surrounding low concentration major silicates. This would constitute a steady-state condition existing in the mantle before the onset of melting. Subsequent preferential melting of the matrix silicates would readily result in the disequilibria observed in basalts.  相似文献   

18.
A new method for the radiogenic isotope (U–Th–Pa–Ra, Sr, Nd, Hf) analysis of the soluble and insoluble components found within ice cores is presented. Melting experiments with rock standards in the presence of EDTA indicate that carbonates, as well as silicates, can be buffered sufficiently to preclude dissolution. The use of EDTA allows adsorbing species, such as Th and Hf, to remain in solution during melting thus fully separating the dust (insoluble) and sea salt (soluble) components of the ice after filtration. A new elemental separation scheme for low sample masses, less than 5 mg solid material, utilizes 4 primary ion exchange columns and two “clean-up” columns to fully isolate U, Th, Pa, Ra, Sr, Nd, and Hf while maintaining high yields. Elution schemes measured for USGS rock standards and a Chinese loess are presented to provide a comparison for variable matrix compositions. Mass spectrometer techniques were modified to measure small aliquots of the standards, equivalent to the amounts found in ice core samples, 10 ng and less. A MC-ICPMS was employed for the measurement of U, Th, Pa, Ra, and Hf; results of the experiments show that with ion yields up to 1%, rock standards have errors for 234U/238U of 1%, 230Th/232Th of 1.5%, [228Ra] of 9%, and 176Hf/177Hf of 100 ppm. MC-TIMS measurements of Sr and Nd show similar errors for small sample sizes: 87Sr/86Sr of 50 ppm and 143Nd/144Nd of 80 ppm. This new analytical method increases the number of possible tracers measured from a single sample, reducing separation times and sample consumption, as well as providing the addition of a radiometric clock, U-series, to the traditional suite of isotopic tracers, Sr, Nd, and Hf.  相似文献   

19.
The Opalinus Clay formation in North Switzerland is a potential host rock for a deep underground radioactive waste repository. The distribution of 238U, 234U and 230Th was studied in rock samples of the Opalinus Clay from an exploratory borehole at Benken (Canton of Zurich) using MC-ICP-MS. The aim was to assess the in situ, long-term migration behaviour of 234U in this rock. Very low hydraulic conductivities of the Opalinus Clay, reducing potential of the pore water and its chemical equilibrium with the host rock are expected to render both 238U and 230Th immobile. If U is heterogeneously distributed in the Opalinus Clay, gradients in the supply of 234U from the rock matrix to the pore water by the decay of 238U will be established. Diffusive redistribution separates 234U from its immobile parent 238U resulting in bulk rock 234U/238U activity disequilibria. These may provide a means of estimating the mobility of 234U in the rock if the diffusion rate of 234U is significant compared to its decay rate. Sampling was carried out on two scales. Drilling of cm-spaced samples from the drill-core was done to study mobility over short distances and elucidate possible small-scale lithological control. Homogenized 25-cm-long portions of a 2-m-long drill-core section were prepared to provide information on transport over a longer distance. Variations in U and/or Th content on the cm-scale between clays and carbonate-sandy layers are revealed by β-scanning, which shows that the (dominant) clay is richer in both elements.  相似文献   

20.
226Ra and other uranium-series radionuclides have been measured in a suite of marine phosphorite samples from the upwelling area off Peru/Chile by gamma-ray spectrometry and radiochemical techniques. Our results lead to the following conclusions: (1) phosphorite nodules typically show unidirectional growth at rates of 1 to 10 mm/Kyr; (2) very young samples (less than a few thousand years) contain slight excess amounts of 226Ra probably derived from pore fluids; and (3) slow but persistent leakage of 226Ra out of phosphate nodules occurs resulting in systematically lower 226Ra ages compared to 230Th ages for samples older than about twenty thousand years. Radium fluxes from these phosphate nodules appear to be 1 to 3 orders of magnitude less than those calculated for deep-sea sediments and ferromanganese nodules.  相似文献   

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