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1.
为了探讨近百年来,人类活动背景下近海沉积物中放射性核素的沉积记录及其对物质输入与埋藏等沉积环境变化的响应,利用γ能谱法对渤海表层和柱状沉积物中的放射性核素238U、226Ra、232Th、210Pb、40K和137Cs进行分析.结果显示,渤海沉积物中放射性核素水平和垂直分布特征明显,铀衰变系核素238U、226Ra和210Pb不平衡,232Th和210Pb受沉积物粒度和有机碳影响显著,238U与226Ra、232Th、40K存在显著相关性.226Ra/238U、232Th/238U和40K/238U比值时空差异显著,渤海沉积物陆源输入影响由西南向东北方向延伸,受河流影响,渤海北部和南部的沉积物输入不稳定,近几十年波动显著.利用210Pbex和137Cs法的测年结果计算获得的渤海近百年来沉积速率在中国近海沉积速率研究背景值范围内;空间上,渤海北部、中部和南部沉积速率处于同一水平,其中北部偏高;时间上,近百年来渤海沉积速率随时间波动,整体上呈现增加趋势,尤其是1980年之后,人类活动影响下渤海沉积速率增加幅度显著,与沉积物输入的波动变化相对应.   相似文献   

2.
U-Pb systems were examined in samples (ranging from 4 to 10 cm3 in volume) of ore material taken from along a 3.5-m profile across a zone of U mineralization exposed in an underground mine at the Strel’tsovskoe U deposit in eastern Transbaikalia. The behaviors of two isotopic U-Pb systems (238U-206Pb and 235U-207Pb) are principally different in all samples from our profile. While the individual samples are characterized by a vast scatter of their T(206Pb/238U) age values (from 112 to 717 Ma), the corresponding T(207Pb/235U) values vary much less significantly (from 127 to 142 Ma) and are generally close to the true age of the U mineralization. The main reason for the distortion of the U-Pb system is the long-lasting (for tens of million years) migration of intermediate decay products in the 238U-206Pb(RD238U) in the samples. This process resulted in the loss of RD238U from domains with high U concentrations and the subsequent accommodation of RD238U at sites with low U concentrations. The long-term effect of these opposite processes resulted in a deficit or excess of 206Pb as the final product of 238U decay. The loss or migration of RD238U are explained by the occurrence of pitchblende in association with U oxides that have higher Si and OH concentrations than those in the pitchblende and a higher +6U/+4U ratio. The finely dispersed character of the mineralization and the loose or metamict texture of the material are the principal prerequisites for RD238U loss and an excess of 206Pb in adjacent domains with low U concentrations. Domains with low U contents in the zone with U mineralization serve as geochemical barriers (because of sulfides contained in them) at which long-lived RD238U(226Ra, 210Po, 210Bi, and 210Pb) were accommodated and subsequently caused an excess of 206Pb. The 235U-207Pb system remained closed because of the much briefer lifetime of the 235U decay products. This may account for the significant discrepancies between the T(206Pb/238U) and T(207Pb/235U) age values. RD238U was most probably lost via the migration of radioisotopes at the middle part and end of the 238U family (starting with 226Ra). The heavy Th, Pa, and U radioisotopes (234Th, 234Pa, 234U, and 230Th) that occur closer to the beginning of 238U decay, before 226Ra, only relatively insignificantly participated in the process. Our results show that the loss and migration of RD238U are, under certain conditions, the main (or even the only) process responsible for the distortion of the U-Pb system.  相似文献   

3.
The study referred to measure activity concentrations of some primordial radionuclides and anthropogenic of 137Cs in soil samples of Mami-water in the Menoua subdivision, Dschang employing gamma-ray spectrometry-based characterized Broad Energy Germanium (BE6350) detector and a comparison of radiological and safety impact parameters on human due to primordial radioactivity in soil with some internationally approved values. In addition, statistical analysis of primordial radionuclides of 226Ra, 232Th and 40K was performed to evaluate the distribution and the interrelation of radionuclides. Samples were randomly collected from a depth of about 0 to 5 cm from the top surface layer. Each of the sampling points was considered as being overlaid with a grid and subdivided into cells. The observed radioactivity level of 226Ra, 232Th and 40K in the investigated soil samples was compared with some published data available in some countries including Cameroon and observed varying within some reported data of radioactivity in soil from bauxite ore deposit. 235U and 137Cs were found in very few samples with a very low average of activity concentrations. In the majority of the samples, the observed radiological safety parameters seem to be greater than the internationally approved values. Consequently, using bricks made of soil as building materials might lead to an increase in radiation risk for the population. Multivariate statistical analysis of activity concentrations of primordial radionuclides performed showed an asymmetrical distribution with more peaked than Gaussian distribution and relatively flatter distribution of radionuclides in soil. In addition, a good positive interrelation between 226Ra and 232Th was observed and a weak negative one observed between 40K and 226Ra–232Th.  相似文献   

4.
The activities of the most common, naturally occurring radionuclides 238U, 226Ra, 210Pb, 228Ra, 228Th, and 40K were measured by gamma-ray spectrometry in samples from reservoir rocks, geothermal fluids, and mineral precipitates at the geothermal research site Groß Schönebeck (North German Basin). Results demonstrated that the specific activity of the reservoir rock is within the range of the mean concentration in the upper earth crust of <800 Bq/kg for 40K and <60 Bq/kg for radionuclides of the 238U and 232Th series, respectively. The geothermal fluid showed elevated activity concentrations (up to 100 Bq/l) for 226Ra, 210Pb, and 228Ra, as compared to concentrations found in natural groundwater. Their concentration in filter residues even increased up to 100 Bq/g. These residues contain predominantly two different mineral phases: a Sr-rich barite (Sr, BaSO4) and laurionite (PbOHCl), which both precipitate upon cooling from the geothermal fluid. Thereby they presumably enrich the radionuclides of Ra (by substitution of Ba) and Pb. Analysis of these precipitates further showed an increased 226Ra/228Ra ratio from around 1–1.7 during the initial months of fluid production indicating a change in fluid composition over time which can be explained by different contributions of stimulated reservoir rock areas to the overall produced fluid.  相似文献   

5.
A method is described for bringing a sediment sample into solution and subsequently carrying out analysis for 210Pb, 226Ra and 137Cs. Silica is removed from the sample by cyclic HNO3HF treatments. 137Cs is separated from 210Ra in a carbonate fusion, extracted by absorption on ammonium molybdophosphate, precipitated directly with BiI3 in presence of citric acid, and β-counted. 210Pb and 226Ra are separated out by 70–75% HNO3 precipitation. Further purification and mutual separation of the two radionuclides is achieved by solvent extraction and anion-exchange techniques. 210Pb and 226Ra are determined by β- and α- counting of their chromate precipitates, respectively, after allowing suitable ingrowth periods for their daughters. The procedural steps effectively eliminate possible interference from other natural or fall-out radioactivities.  相似文献   

6.
Characterizing the dynamics of fluvial sediment sources over space and time is often critical in identifying human impacts on fluvial systems. Upland interfluve and subsoil sources of suspended sediment at Loco Bayou, Texas, were distinguished using 226Ra/232Th, 226Ra/230Th and, 228Ra/232Th. Source contributions were apportioned at three stations during within-bank and flood flows. 137Cs and 210Pbxs (excess 210Pb) were used to determine floodplain sedimentation; suspended sediment 210Pbxs/137Cs data mirrored results of Ra/Th, showing dominance of subsoil sources during within-bank flows, changing to interfluve sources during flood. This trend corresponds spatially to influx of sediment from ephemeral tributaries, reflecting mobilization of stored interfluvial sediments during flood stage. Upper basin sedimentation was similar but markedly less at the lowermost station. These results indicate (1) modified ephemeral tributaries store sediment derived from sheet wash, discharging them during flood, and (2) southernmost Loco Bayou is episodically re-worked, resulting in significantly reduced local rates of sedimentation.  相似文献   

7.
Gamma activity from the naturally occurring radionuclides namely, 226Ra, 232Th, the primordial radionuclide 40K was measured in the soil of Cuihua Mountain National Geological Park, China using γ-ray spectrometry technique. The mean activity of 226Ra, 232Th and 40K were found to be 27.2 ± 6.5, 43.9 ± 6.2 and 653.1 ± 127.6 Bq kg−1, respectively. The concentrations of these radionuclides were compared with the typical world values and the average activities of Chinese soil. The radium equivalent activity, the air absorbed dose rate, the annual effective dose rate, and the external hazard index were evaluated and compared with the internationally approved values. All the soil samples have Raeq lower than the limit of 370 Bq kg−1 and H ex less than unity. The overall mean outdoor terrestrial gamma dose rate is 66.3 nGy h−1 and the corresponding outdoor annual effective dose is 0.081 mSv.  相似文献   

8.
The variation of the natural radionuclide concentrations depends on the chemical composition of each site. In this work, two thermal springs in the east of Algeria have been chosen to assess the activity concentration of natural radionuclide, mainly the three natural radioactive series 238U, 235U and 232Th, and 40K. The high-resolution gamma ray spectroscopy was used to determine these concentrations. In these water samples, 235U, 234Th, 210Pb, 226Ra radionuclides are less than the minimum detectable activity. The activity of 238U is dominant. The 238U activity was determined by taking the mean activity of two separate photo-peaks of daughter nuclides 214Pb at 351.92 (37.2%) keV and 214Bi at 609.31 (45%) keV. The measured activity concentrations of 238U in water samples obtained from the concentrations of 214Bi and 214Pb ranged from 0.56 ± 0.20 to 1.13 ± 0.20 Bq/L. The annual effective dose value due to the ingestion of the measured radionuclide 238U in 1 L of water, for an adult, ranged from 9.20 to 18.56 µSv.  相似文献   

9.
Several water and surface microlayer samples from Lake St. Clair, the Niagara River, and the North Shore of Lake Ontario collected during 1983–1986 have been assayed for a variety of radionuclides. In addition, the foam accumulating in the pool just below Niagara Falls was also analyzed and found to be the most efficient aqueous phase collector of137Cs,210Pb, and226Ra.The order of radioisotope specific activities from highest to lowest is: Lake Ontario sediment, Niagara River suspended solids, Niagara River foam, surface microlayer water, and subsurface water. Radiological dose rates to the sediments from137Cs,226Ra, and228Th total about 5 mGy/y.  相似文献   

10.
厦门火烧屿裸露岩石的铀放射系不平衡   总被引：2，自引：1，他引：2  
用HPGeγ谱方法测定了厦门火烧屿裸露岩石天然放射性核素^40K、^228Ra、^228Th、^238U、^226Ra和^210Pb含量，对其铀系不平衡关系进行了讨论，发现钍系核素^228Ra和^228Th基本上是平衡的，而大部分样品^226Ra相对于^228U、^210Pb相对于^226Ra亏损。由此推论，水体作用下岸边岩石中^226Ra直接进入水体，可以是海水中^226Ra的一个来源；岸边岩石中^222Rn逸出后，衰变^210Pb再进入水体，可以是海水中^210Pb的一个来源。  相似文献   

11.
Levels of naturally occurring radioactivity in sediment samples of Beni Haroun dam have been investigated. The activity concentrations of 238U and 232Th decay chains and 40K primordial radionuclide have been measured using high-resolution HPGe detector. Activity concentrations of 226Ra, 232Th, and 40K radionuclides were found in the ranges 9–66, 14–37, and 177–288 Bq/kg with the mean values 24.67, 25.98, and 208.10 Bq/kg, respectively. Radiological hazard parameters were estimated based on the activity concentrations for 226Ra, 232Th, and 40K to find out any radiation hazard associated with the sediments. Correlation studies between pairs of radionuclides were performed and discussed, and the obtained results are compared with international recommended values.  相似文献   

12.
Phonolite pumice found floating offshore of Tristan da Cunha following intense seismic activity southeast of the island July 29-30, 2004 was analyzed for 238U- and 232Th-series nuclides to determine initial 230Th, 226Ra, 210Pb, 210Po, 228Ra, and 228Th activities. The initial (210Po/210Pb) value of 0.15 for the phonolite shows that, like most subaerial lavas, this subaqueous tephra degassed most of its 210Po upon eruption. The (230Th/232Th) and (238U/232Th) values for the phonolite are similar to those of the trachyandesites erupted in 1961 from Tristan da Cunha. However, the relative activities of 210Pb, 226Ra, and 230Th in the phonolite contrast with those of the trachyandesites, in that 210Pb and 230Th are both strongly enriched with respect to 226Ra. In addition, the phonolite had a small deficit in 228Ra with respect to 232Th. The Ra deficits likely resulted from partitioning into feldspars and hornblende in a time frame that extended over several decades to a century. These disequilibria can be explained by crystal fractionation at a decreasing rate through time at an average of 3-5 × 10−3 year−1. The calculated crystallization rate is about an order of magnitude faster than has been calculated for most other phonolites and trachytes, and about half that calculated for crystallization of the Makaopuhi lava lake. These data imply that the 2004 magma was not the differentiated cap of a much larger body that remained at depth. Instead, it was likely the residue of a relatively small body of more mafic magma that was injected into the crust southeast Tristan and underwent extensive and rapid crystal fractionation before it erupted.  相似文献   

13.
Tailings resulted from sulphuric acid leaching process of uranium from sedimentary rocks contain high concentrations of 226Ra and its daughters, the most important of which is 222Rn. Movement of radon gas out of the tailings is strongly influenced by the physicochemical characteristics of these tailings especially their radium content and the grain size. So, the tailing samples were size fractionated into four sizes (>?250, 250–125, 125–74 and <?74 µm). The natural radioactivity was investigated using hyper-pure germanium detector and solid-state nuclear track detectors (CR-39) for bulk size and after size fractionation. The activity concentrations of different radionuclides in size-fractionated tailing samples have been shown to be strongly dependent on the size of the particles. In the range of >?250 and <?74 µm, the activity concentrations of 230Th, 226Ra, 214Pb, 214Bi, 210Pb, 232Th and 40K increased throughout with decreasing particle size, while that of 238U, 234U and 235U have an opposite effect. The results revealed an inverse relationship between the radon exhalation rate and size fractionation. Also, the results showed a good correlation between radium activity concentration and radon mass exhalation rate.  相似文献   

14.
Concentrations of 137Cs, 210Pb, 226Ra, U, V, Pb, Cd and Hg have been measured in firn and ice deposited during the past three decades in accumulation zones of glaciers and also in pre-industrial glacier ice collected in Spitsbergen, Northern Norway, Alaska, Southern Norway, Alps, Himalayas, Ruwenzori, Peruvian Andes, and at King George Island in Antarctica. Except for Hg, the geographical distribution of mean concentrations of 226Ra, U and stable heavy metals in contemporary ice is not uniform, with the lowest concentrations found in Northern Norway, Alaska and Antarctica, and the highest in continental locations at equatorial and middle latitudes. We did not find evidence of changes in rate of metal deposition during the last three decades, as compared with pre-industrial period, however, our samples of pre-industrial ice might be contaminated in part by contemporary fallout migrating from the exposed surface of old parts of glaciers into the deeper ice layers. Using the data on annual injections of 137Cs into the global atmosphere and mean global concentrations of radionuclides and heavy metals found in contemporary ice the global annual flows of 226Ra, 210Pb, U,V, Pb, Cd and Hg were estimated as 6.6 kCi, 485 kCi, 12kt, 4870kt, 590 kt, 180 kt and 190 kt, respectively. These estimates are 1–2 orders of magnitude higher than estimates based on primary paniculate emissions. The anthropogenic contribution is a small fraction of the flows, which are dominated by natural processes leading to enrichment of metals in airborne dust.  相似文献   

15.
The study was conducted for the investigation of amount of radioactivity in the barren and cultivated soil of Bio saline Research Station in Pakka Anna, established by Nuclear Institute for Agriculture and Biology (NIAB) in 1990, 34 km. away from the city of Faisalabad, in the Punjab province of Pakistan. The studies were done on an area of about 100 hectares of two types of virgin and fertilized saline soils. The technique of gamma ray spectrometry was applied using HPGe (high purity germanium) gamma ray detector and a PC based MCA. Activity concentration levels due to 40K, 137Cs, 226Ra and 232Th were measured in 250 saline soil samples collected at a spacing of about 4 hectares at the depth level of 0–25 cm. with a step of 5 cm. depth. Activity concentrations ranges of the concerned radionuclides for both of the soils were as follows: 40K, for virgin and cultivated saline soil was 500–610.2 and Bq/kg 560.2–635.6 respectively; 137Cs, 3.57–3.63 and 1.98–5.15 Bq/kg 238U, 26.3–31.6 and 30.3–38.7 Bq/kg, and 232Th, 50.6–55.3 and 50.6–64.0 Bq/kg respectively. The absorbed dose rate in air lies in the region 63–73 nGyh-1 and 68–83 nGyh-1 for virgin and fertilized soils respectively. This indicates that this region lies in the area of higher radiation background, while comparing with the worlds’ average. The slightly higher value of dose in the fertilized farm may be due to the use of fertilizers for cultivation. Before the radiometric measurements, chemical analysis for concentration of Na, Ca and Mg was also carried out along with the measurement of electrical conductivity and pH of the soil samples.  相似文献   

16.
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   

17.
This paper describes the use of 210Pb and 137Cs radioactivity measurements to determine the rates of sedimentation in the Great Lakes. Cores from eight locations in Lake Michigan were chosen for examination to cover as wide as possible a range of sedimentation rates and representative sedimentary environments. The surficial 210Pb activity in the sediments varies between 7 and 23 pCi/g dry wt and its profile in each core shows the expected exponential decrease with depth consistent with the assumption of uniform sedimentation rate over the last hundred years and secular equilibrium between supported 210Pb and 226Ra (0.5-1.0 pCi/g dry wt). Companion measurements of 137Cs indicate that the coring technique satisfactorily recovered the uppermost levels of the deposit and that the mobility of both radionuclides within the sediment is probably small.Based on the limited number of cores analyzed to date, it appears that modern sedimentation rates are not very different from average rates for the last 7000 yr. The excess 210Pb appears to originate primarily from atmospheric fallout, but a further inventory of the 210Pb distribution over the lake bottom must be made to properly assess the significance of other sources. The spatial distributions of both 137Cs and 210Pb at certain stations suggest that the mode of transport of these radionuclides are comparable and involve attachment to settling particles. A mathematical model is developed which accounts for the observed limited mobility of both 210Pb and 137Cs in several of the cores in terms of post-depositional redistribution by physical or biological mixing processes.  相似文献   

18.
《Applied Geochemistry》1999,14(3):365-385
The abundance and chemical/mineralogical form of 226Ra, 238U and 232Th were determined on samples of soil and associated vegetation at 12 sites in the eastern United States. Progressive, selective chemical extraction plus size fractionation determined the abundance and radiometric equilibrium condition of these nuclides in 6 operationally defined soil fractions: exchangeable cations, organic matter, “free” Fe-oxides, sand, silt, and clay.In soils, profile-averaged 226Ra/238U activity ratios (AR) are within 10% of unity for most sites, implying little fractionation of U and Ra when the entire soil profile is considered. However, 226Ra greatly exceeds 238U activity in most surface soil (AR up to 1.8, av 1.22), in vegetation (AR up to 65, av. 2.8), in the exchangeable+organic fraction (AR up to 30, av. 13), in some soil Fe oxides (AR up to 3.5, av. 0.83) and in the C horizons of deeply weathered soils (AR up to 1.5).A major factor in Ra behavior is uptake by vegetation, which concentrates Ra>U and moves Ra from deeper soil to surface soil. Vegetation is capable of creating the observed Ra excess in typical surface soil horizons (AR up to 1.8, av. 1.22) in about 1000 a. Of the total Ra in an average A horizon, 42% occurs as exchangeable ions and in organic matter, but only 6–8% of the parent U and Th occur in these soil forms. In contrast, U is slightly enriched relative to Ra in Fe-oxides of A horizons, implying rapid chemical partition of vegetation-cycled U and Ra.In deeper horizons, transfer by vegetation and/or direct chemical partitioning of Ra into organic and exchangeable forms provides a source for unsupported 226Ra in Ra-rich organic matter, and leaves all soil minerals Ra-poor (AR=0.73). Organic matter evidently has a strong affinity for Ra.The phenomena discussed above are relevant to evaluation of indoor Rn hazard, and behavior of Ra at sites affected by radioactive waste disposal, phosphate tailings, Ra-rich brine, and uraniferous fertilizer.  相似文献   

19.
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   

20.
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   

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