An analysis of naturally occurring radionuclides and <Superscript>137</Superscript>Cs in the soils of urban areas using gamma-ray spectrometry

This study of environmental radioactivity was carried out in the soils of an urban area. Naturally occurring gamma-emitting radionuclides and man-made ¹³⁷Cs were found in the soil profiles collected from four parks in the central Belgrade city area and the soil layer was examined every 10 cm and to a depth of 50 cm. Radioisotope activity concentrations (Bq kg^?1) in the samples of urban soil using the gamma-ray spectrometry method were in the range of 14–46 for ²³⁸U, 33–50 for ²²⁶Ra, 29–63 for ²¹⁰Pb, 1.2–3.4 for ²³⁵U, 28–50 for ²³²Th, 424–576 for ⁴⁰K and 0.7–35.8 for ¹³⁷Cs. Some of the basic physicochemical soil properties (pH, organic matter content, calcium-carbonate content, particle size distribution) were determined to investigate the impact on the vertical distribution of radionuclides. The results of this investigation showed that variations of activity concentration ratios of radionuclides that belong to the same (²³⁸U/²²⁶Ra) or different radioactive series (²³²Th/²²⁶Ra; ²³⁵U/²³⁸U), including ²¹⁰Pb/¹³⁷Cs ratios could well be explained by the properties of the soil. Alkaline pH reaction, the accumulation of organic matter in the uppermost and of carbonates in the deepest layers of urban soil had an effect on ²³⁸U/²²⁶Ra, and ²¹⁰Pb/¹³⁷Cs activity concentration ratio values, while ²³²Th/²²⁶Ra and partially ²³⁵U/²³⁸U ratios were associated with the particle sizes vertical distribution. A study of radionuclides in the samples of leaves of two deciduous tree species common for these parks was also conducted and ²¹⁰Pb and ⁴⁰K were found concentrated in leaves rather than other investigated radionuclides.     

厦门火烧屿裸露岩石的铀放射系不平衡

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。     

Natural radioactivity levels and evaluation of radiological hazards from Beni Haroun dam sediment samples,northeast Algeria

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.     

Natural radionuclide concentrations in thermal springs of east Algeria

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.     

U- and Th-decay series constraints on the timescales of crystal fractionation to produce the phonolite erupted in 2004 near Tristan da Cunha, South Atlantic Ocean

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.     

Estimation of excess lifetime cancer risk and radiation hazard indices in southern Iraq

Relatively high activity concentrations of some radionuclides (²²⁶Ra, ²³⁸U, ²³²Th, and ⁴⁰K) have been measured in surface and subsurface soils in areas (southern Iraq) where many warfare actions have taken place during the Iran–Iraq and Gulf wars. Such high activity concentrations might be related to the increase in cancerous injuries and birth defects recently reported. The study was aimed to estimate the activity concentrations of some nuclides and a comparison of results with international health hazard indices. In addition, the excess lifetime cancer risk (ELCR) was assessed. Soil samples were collected at three depths (0, 30, and 60 cm) in three locations in Abu Al Khasib and Ad Dayr in Basrah governorates. The average activity concentrations were estimated employing hyper-pure germanium HPGe gamma-ray detection technology. The values obtained in Abu Al Khasib were: 58.44 Bq/kg (²²⁶Ra), 43.56 Bq/kg (²³⁸U), 19.38 Bq/kg (²³²Th), and 321.76 Bq/kg (⁴⁰K) whereas in Ad Dayr 45.71 Bq/kg (²²⁶Ra), 35.53 Bq/kg (²³⁸U), 20.33 Bq/kg (²³²Th), and 337.02 Bq/kg (⁴⁰K). According to UNSCEAR (Sources and effects of ionizing radiations: a report on the effects of atomic radiation to the general assembly with scientific annexes, Annex B, United Nations, New York, 2000) report, higher levels of ²²⁶Ra, ²³⁸U concentrations than the world’s average values (35 Bq/kg) were observed in both locations. In addition, some radiation hazard indices were determined for both locations: average outdoor external dose (D _out), average indoor external dose (D _in), total average value of the external dose (D _tot), average annual outdoor effective dose (E _out), average annual indoor effective dose (E _in), and averaged total annual effective dose (E _tot). Values for D _tot and E _tot were higher than the worldwide median (143 nGy/h and 0.48 mSv/y, respectively) in both regions. The measured values of activity concentrations were also used to estimate the outdoor, indoor, and total ELCR. The ELCR values were higher than the worldwide averages. Further analyses and studies need to assess the real risks for human health and possible soil remediation.     

Evaluation of dose parameters and radiological hazards in gravel samples of Konyaaltı Beach,Antalya

It is important to know the distribution and transfer of radionuclides such as uranium, thorium, and potassium, which exist naturally in the environment we live in. For this reason, measurements of these natural radionuclides have been carried out for 15 gravel samples collected from Konyaalt? Beach, Antalya. In order to measure the natural activity concentrations of potassium-40, uranium-238, and thorium-232 radionuclides, we performed the measurements by applying a gamma spectrometry method with a “3?×?3” NaI(Tl) detector, which is a multichannel analytical detector in the Suleyman Demirel University gamma spectrometry laboratory. The minimum, maximum, and mean values for the ²²⁶Ra activity concentration were measured as 19.74 Bq/kg, 37.03 Bq/kg, and 31.64 Bq/kg, respectively. The minimum, maximum, and mean values for the ²³²Th activity concentration were measured as 12.76 Bq/kg, 34.32 Bq/kg, and 26.67 Bq/kg, respectively. The minimum, maximum, and mean values for the ⁴⁰K activity concentration were measured as 196.37 Bq/kg, 421.13 Bq/kg, and 350.42 Bq/kg, respectively. Dose parameters and radiation damage indices were calculated using experimentally measured activity results and the resulting dose and hazard index values were compared with the determined limit values. It can be concluded that no risk may threat in terms of the hazard index values. In addition, all results obtained in terms of calculated dose values except for annual gonadal dose are below the recommended limit values.     

Anomalous concentrations of radionuclides in the groundwater of Ede area,southwestern Nigeria: a direct impact of geology

An assessment of the groundwater in areas underlain by pegmatite in Ede, southwestern Nigeria was carried out to determine the concentration of Potassium-40 (⁴⁰K), Uranium-238 (²³⁸U) and Thorium-232 (²³²Th) radionuclides. In the earlier work, it was established that zircons in these pegmatites have suffered a high degree of metamictization that has enhanced continuous loss of some radionuclides since the time of emplacement of the pegmatite host rock to the present. The aim of this work is to determine whether or not there is corresponding increase in the concentration of radionuclides in groundwater in the study area. Fifteen groundwater samples were collected from both hand dug wells and boreholes in the area. Ten samples were from Ede town, two samples each from nearby communities of Iddo and Ekuro and one from Iwoye, where the bedrocks were not pegmatites. All the 15 samples were analyzed with the Sodium Iodide scintillator (NaI [Tl]) detector at the Centre for Energy Research and Development, Obafemi Awolowo University, Ile-Ife, Nigeria. The results showed varying concentrations of the radionuclides in the water samples. Activity concentrations of Potassium-40 (⁴⁰K) indicated an average value of 17.149 Bq/L for samples from Ede, 9.265 Bq/L for Iddo, 6.6 Bq/L for Ekuro, while Iwoye has a value of 21.21 Bq/L. The Uranium-238 (²³⁸U) series had an average value of 13.64 Bq/L for Ede, 13.49 Bq/L for Ekuro, 11.685 Bq/L for Iddo and 12.04 Bq/L for the lone sample from Iwoye. Thorium-232 (²³²Th) series had an average value of 11.182 Bq/L for Ede, while average values of 7.79 Bq/L and 9.025 Bq/L, respectively, were recorded for Iddo and Ekuro and 12.25 Bq/L for Iwoye. The annual effective dose level of ⁴⁰K is generally below the World Health Organization (WHO) recommended dosage of 0.1 mSv/y except for three locations, while those of ²³⁸U and ²³²Th are in excess of the standard values. The high radionuclides in the groundwater in the study area were not due to anthropogenic sources but directly due to geological processes which release the radioisotopes from rocks after weathering, continuous loss from metamict minerals and natural lateral mobility from regions of radionuclides’ release to other areas. There is thus the need to carry out systematic studies of the radionuclides concentrations on regional scale in the area which could lead to investigating on both short- and long-term health effects on organic species in these areas, and development of purification systems before utilizing water from the areas for domestic and industrial purposes.     

渤海沉积物中放射性核素分布及其对沉积环境变化的响应

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210Pb_ex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.      

Determination of 210Pb, 226Ra and 137Cs in sediments

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.     

Radionuclide partitioning across great lakes natural interfaces

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.     

Lead precipitates from natural gas production installations

Over the last few years various lead precipitates have been found in natural gas production installations in north-western Europe during routine cleaning operations. We have studied the composition and morphology of these precipitates and will discuss the probable depositional processes. The lead precipitates can be divided into three categories based on morphology and composition. (1) Thin, crustal precipitates containing metallic lead, barite and galena. These precipitates originate from untreated gas–water mixtures, and are found in pipes throughout production installations. (2) Annular, homogeneous precipitates of metallic lead, formed from separated production water in pumps of production installations. (3) Suspended precipitates which are found either in the well tubing, or in pipes or valves downstream from the installations, originating from untreated gas–water mixtures. All lead precipitates contain ²¹⁰Pb, whereas precipitates of both lead and barite contain ²²⁶Ra as well. These naturally occurring radionuclides are most likely derived from ²³⁸U-enriched organic sediments or ²²⁶Ra-enriched precipitates in or near the gas reservoirs.     

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

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

Dependence of radon exhalation on grain size of sedimentary waste

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.     

Natural radioactivity distribution and gamma radiation exposure of beach sands from Sithonia Peninsula

This study aims to evaluate the activity concentrations of ²³⁸U, ²²⁶Ra, ²³²Th, ²²⁸Th and ⁴⁰K along the beaches of Sithonia Peninsula which are adjacent to the rock-types of the Sithonia Plutonic Complex. These range from 6–673, 5–767, 5–1750, 6–1760 and 185–875 Bq/kg respectively. The (% wt.) heavy magnetic (HM) fraction (epidote, allanite, hornblende, biotite and garnet), the heavy non-magnetic (HNM) fraction (monazite, zircon, titanite and apatite) and the total heavy (TH) fraction, were correlated with the concentrations of the measured radionuclides in the bulk samples. The HNM fraction seems to control the activity concentrations of ²³⁸U in all samples, while the HM fraction, at least for the heavy mineral rich samples bearing high amounts of epidote crystals with allanite cores, controls their ²³²Th content. The measured radionuclides in beach sands were normalized to the respective values measured in the granitic rocks, which are their most probable parent rocks, in order to provide data on their enrichment or depletion. The annual effective dose varies from 0.013 to 0.688 mSv y^?1 for local people working on the beach, while for tourists the annual external effective dose ranges between 0.003 and 0.165 mSv y^?1.     

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

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

An investigation about natural radioactivity,hydrochemistry, and metal pollution in groundwater from Calabrian selected areas,southern Italy

The increasing interest in radioactivity has brought about the need for an assessment of human exposure to radiation. It is, therefore, necessary to examine naturally occurring radioactivity in the environment, especially its occurrence in groundwater. The aim of this work was then to study the levels and behavior of the most significant natural radionuclides, also in order to improve the knowledge of the hydrochemical processes involved in the selected groundwater systems. Natural radioactivity in fifteen Calabrian groundwaters for human use was investigated through high-resolution gamma spectrometry (with a negative-biased Ortec HPGe detector) and liquid scintillation measurements. Particular attention was given on those radionuclides (³H, ²³⁸U, ²²⁶Ra, and ²²⁸Ra), which contribute in a significant way to the overall effective dose received by members of the public due to the intake of drinking water originating from groundwater systems. The activity concentration of ²³⁸U varied from 1 to 51 mBq/L, as a result of the geology of the investigated area and of the oxidizing conditions that favored U dissolution. ²²⁶Ra presented a broad range of activity concentrations (0.011–0.14 mBq/L), lower than uranium ones because radium occurs in groundwater under reducing conditions. Some heavy metals (Cd, Pb, Be, Hg, Ag, As, Tl, Sb, Se, and Ni) were also investigated through ICP-MS measurements and compared with the limits set by the Italian Legislation. Metals are released into the environment by both natural and anthropogenic sources; they leach into underground waters, moving along water pathways and eventually depositing in the aquifer.     

Distribution of natural uranium,thorium, lead,and polonium radionuclides in tidal phases of a Delaware salt marsh

Natural radionuclides in the uranium and thorium series were measured in solid tidal phases (suspended particles, bottom sediment, surface microlayer colloids) of a salt marsh in lower Delaware. The purpose was to identify potential processes responsible for trace element cycling (sources, redistribution and exchange) in salt water marshes and with their coastal waters. Generally, concentrations of U, Th,²¹⁰Pb, and²¹⁰Po on the tidal solid phases suggest a general mechanism by which tidal marshes appear to be trapping the nuclides into their interiors. The processes may include transport of enriched fine particles into the marsh, capture by salt marsh grass and chemical fixation by redox processes at the sediment surface. Specifically, the uranium contents of most of the samples are similar with activity ratios²³⁴U²³⁸U≧1, indicating a mixture of detrital and nondetrital (authigenic) uranium inputs such as seawater or ground water. Since the²³⁰Th daughter is generally deficient by about 50%, the authigenic enrichment process appears to favor uranium and is potentially linked to the extensive diagenetic sulfur redox cycle of salt marsh sediments. The²¹⁰Po/²¹⁰Pb activity ratio is less than one on Spartina adsorbed solids, and could suggest a general process in salt marshes which favors²¹⁰Pb enrichment by atmospheric fallout over enrichment of²¹⁰Po on time scales of weeks which correspond to complete tide marsh exchange. A²²⁸Th/²³²Th activity ratio of less than unity on the solids adsorbed onto marsh grass suggests a net process whereby diffusive loss of the intermediate daughter²²⁸Ra from the adsorbed solids to tidal waters dominates over potential²²⁸Th scavenging by suspended sediment.     

Factors controlling the groundwater transport of U, Th, Ra, and Rn

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 ϰ_i, characteristic of each nuclide. Where ϰ_i 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 ratio^ɛ234Th/^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.     

U-series disequilibria in Kick’em Jenny submarine volcano lavas: A new view of time-scales of magmatism in convergent margins

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.