Science.gov

Sample records for 238u 234u 226ra

  1. Biological availability of (238)U, (234)U and (226)Ra for wild berries and meadow grasses in natural ecosystems of Belarus.

    PubMed

    Sokolik, G A; Ovsiannikova, S V; Voinikava, K V; Ivanova, T G; Papenia, M V

    2014-01-01

    This work is devoted to investigation of behavior of (234)U, (238)U and (226)Ra by determining the soil to plant transfer under different natural conditions such as forest or swamped areas and meadow lands with different soil types. The paper summarizes the data on investigation of uranium and radium uptake by wild berries and natural meadow grasses in the typical conditions of Belarus. Parameters characterizing the biological availability of (234)U, (238)U and (226)Ra for bilberry (Vaccinium myrtillus), lingonberry (Vaccinium viti-idaea), blueberry (Vaccinium iliginosum) and cranberry (Vaccinium oxycoccus palustris) as well as for widely occurring mixed meadow vegetation, which belongs to the sedge-grass or grass-sedge associations and forbs, have been established. In the sites under investigation, the deposition levels of (238+239+240)Pu were less than 0.37 kBq m(-2) and (137)Cs deposition ranged between less than 0.37 and 37 kBq m(-2). It was found that activity concentrations of radionuclides in berries varied in the ranges of 0.037-0.11 for (234)U, 0.036-0.10 for (238)U and 0.11-0.43 Bq kg(-1) for (226)Ra, but in the mixed meadow grasses they were 0.32-4.4, 0.24-3.9 and 0.14-6.9 Bq kg(-1) accordingly. The (234)U/(238)U activity ratios were 1.02 ± 0.01 for wild berries, 1.20 ± 0.09 for underground meadow grasses and 1.02 ± 0.02 for proper soils. The concentration ratios (CRs, dry weight basis) of (234)U and (238)U for mixed meadow grasses were 0.036-0.42 and 0.041-0.46 respectively. The correspondent geometric means (GM) were 0.13 and 0.15 with geometric standard deviations (GSD) of 2.4. The CRs of (226)Ra for meadow grasses were 0.031-1.0 with GM 0.20 and GSD 2.6. The CRs of (234)U, (238)U and (226)Ra for wild berries ranged within 0.0018-0.008 (GM is 0.0034, GSD is 1.8), 0.0018-0.008 (GM is 0.0035, GSD is 1.8) and 0.005-0.033 (GM is 0.016, GSD is 2.1) accordingly. The highest CR values of uranium for mixed meadow grasses were found in the

  2. Study on the radioactivity and soil-to-plant transfer factor of (226)Ra, (234)U and (238)U radionuclides in irrigated farms from the northwestern Saudi Arabia.

    PubMed

    Al-Hamarneh, Ibrahim F; Alkhomashi, N; Almasoud, Fahad I

    2016-08-01

    The present study addresses the soil-to-plant transfer factors (TFs) of (226)Ra, (234)U and (238)U for 13 types of vegetables and agricultural crops planted under semi-arid environment in the northwestern part of Saudi Arabia. Crop plants along with plant-growing soils were collected from selected farms, which are irrigated from the non-renewable Saq aquifer, and investigated for their radioactivity content by means of alpha spectrometry after applying a radiochemical separation procedure. Hence, TF data for plant roots, green parts (stem and leaves) and fruits were calculated and contrasted to those reported in the literature. Substantial differences were observed in the TFs of Ra and U radioisotopes among plant species. In crop fruits, eggplant exhibited the highest uptake of (226)Ra (TF value of 0.11), while beans (0.16) have the highest TF for (234)U and (238)U. The geometric mean TF values indicated that the crop roots tend to accumulate Ra and U about four to six-folds higher than fruits. The relation between TF values and soil concentrations showed a weak correlation. Activity ratios between radionuclides in crop plants indicated the preferential translocation of U in fruits than Ra even though Ra is more available for root uptake. The fruit/root (F/R) ratios obtained for the investigated plants shown that pepper had the smallest F/R ratios (0.07 ± 0.01, 0.12 ± 0.02 and 0.11 ± 0.02 for (226)Ra, (234)U and (238)U, respectively), while the highest F/R ratios were observed in potatoes (0.71 ± 0.15, 0.44 ± 0.10 and 0.40 ± 0.08 for (226)Ra, (234)U and (238)U, respectively). The TF and F/R ratios data of natural radionuclides in the study region can hopefully improve the scientific knowledge for future studies.

  3. Ground water contamination with (238)U, (234)U, (235)U, (226)Ra and (210)Pb from past uranium mining: cove wash, Arizona.

    PubMed

    Dias da Cunha, Kenya Moore; Henderson, Helenes; Thomson, Bruce M; Hecht, Adam A

    2014-06-01

    The objectives of the study are to present a critical review of the (238)U, (234)U, (235)U, (226)Ra and (210)Pb levels in water samples from the EPA studies (U.S. EPA in Abandoned uranium mines and the Navajo Nation: Red Valley chapter screening assessment report. Region 9 Superfund Program, San Francisco, 2004, Abandoned uranium mines and the Navajo Nation: Northern aum region screening assessment report. Region 9 Superfund Program, San Francisco, 2006, Health and environmental impacts of uranium contamination, 5-year plan. Region 9 Superfund Program, San Franciso, 2008) and the dose assessment for the population due to ingestion of water containing (238)U and (234)U. The water quality data were taken from Sect. "Data analysis" of the published report, titled Abandoned Uranium Mines Project Arizona, New Mexico, Utah-Navajo Lands 1994-2000, Project Atlas. Total uranium concentration was above the maximum concentration level for drinking water (7.410-1 Bq/L) in 19 % of the water samples, while (238)U and (234)U concentrations were above in 14 and 17 % of the water samples, respectively. (226)Ra and (210)Pb concentrations in water samples were in the range of 3.7 × 10(-1) to 5.55 × 102 Bq/L and 1.11 to 4.33 × 102 Bq/L, respectively. For only two samples, the (226)Ra concentrations exceeded the MCL for total Ra for drinking water (0.185 Bq/L). However, the (210)Pb/(226)Ra ratios varied from 0.11 to 47.00, and ratios above 1.00 were observed in 71 % of the samples. Secular equilibrium of the natural uranium series was not observed in the data record for most of the water samples. Moreover, the (235)U/(total)U mass ratios ranged from 0.06 to 5.9 %, and the natural mass ratio of (235)U to (total)U (0.72 %) was observed in only 16 % of the water samples, ratios above or below the natural ratio could not be explained based on data reported by U.S. EPA. In addition, statistical evaluations showed no correlations among the distribution of the radionuclide concentrations

  4. Activity ratios of (234)U/(238)U and (226)Ra/(228)Ra for transport mechanisms of elevated uranium in alluvial aquifers of groundwater in south-western (SW) Punjab, India.

    PubMed

    Kumar, A; Karpe, R K; Rout, S; Gautam, Y P; Mishra, M K; Ravi, P M; Tripathi, R M

    2016-01-01

    The concentrations of total dissolved uranium (U), its isotopic composition ((234)U, (235)U, (238)U) and two long lived Ra isotopes ((226)Ra and (228)Ra) in alluvial aquifers of groundwater were determined to investigate the groundwater flow pattern in the south-western (SW) Punjab, India. Particular attention was given to the spatial variability of activity ratios (ARs) of (234)U/(238)U and (226)Ra/(228)Ra to predict the possible sources and supply process of U into the water from the solid phase. The measured groundwater (234)U/(238)U ARs were ∼1 or >1 in the shallow zone (depth < 30 m) with high U concentration and <1 in the deeper zone (depth > 30 m) with relatively low U concentration. The simultaneous elevated U concentration and (234)U/(238)U ARs in waters were possibly due to differences in imprints of rock-water interactions under hydrologic conditions. However, (234)U/(238)U ARs < 1 clearly indicate the lack of recharge from surface water to groundwater leading to (234)U deficit in groundwater. This deficit might be also attributed to alpha recoil processes under strong dissolution. Overall, the decreasing pattern of (234)U/(238)U ARs observed from SE to SW or NW ward clearly indicates a groundwater flow paths from SE to SW/NW. Similarly, (226)Ra/(238)U ARs < 1 for all water samples reflect that the precursor (238)U is fairly mobile relative to (226)Ra. This might be due to unusually high amount of (238)U in groundwaters and subsequently the different geochemistry of the two isotopes. On the other hand, (226)Ra/(228)Ra ARs in groundwaters varied widely and observed about 50-300 times higher than (238)U/(232)Th ARs in granitic rocks or soils. Such elevation in ARs might be attributed to different dissolution properties of their parents during water-rock interactions or lattice damage during decay or local enrichments of uranium in the aquifers.

  5. 234U /238U and 230Th /234U activity ratios in mineral phases of a lateritic weathered zone

    NASA Astrophysics Data System (ADS)

    Lowson, Richard T.; Short, Stephen A.; Davey, Brian G.; Gray, David J.

    1986-08-01

    A selective phase extraction procedure was developed for the identification of the significant phases of a typical deep soil profile sampled in the vicinity of the Ranger No. 1 uranium ore body, Alligator Rivers region, N.T., Australia. The significant phases were identified as amorphous iron oxide, crystalline iron oxide and a clay/quartz resistate. The distribution of 238U, 234U, 230Th and 226Ra between the phases was measured. The results indicated that the amorphous iron oxide phase is in adsorption/desorption equilibrium with the ground water. The crystalline iron oxide phase contains a chemical control, the kinetics of which are commensurate with or less than the half-life of 230Th (7.52 × 10 4 y). The clay/quartz resistate is enriched in 238U descendants in such a way that they are not readily accessible to the ground water.

  6. Influence of soil structure on the "Fv approach" applied to (238)U and (226)Ra.

    PubMed

    Blanco Rodríguez, P; Vera Tomé, F; Lozano, J C

    2017-02-01

    The soil-to-plant transfer factors were determined in a granitic area for the two long-lived uranium series radionuclides (238)U and (226)Ra. With the aim to identify a physical fraction of soil whose concentration correlates linearly with the plant concentration, the soil compartment was analyzed in various stages. An initial study identified the soil compartments as being either bulk soil or its labile fraction. The bulk soil was subsequently divided into three granulometric fractions consisting of: coarse sand, fine sand, and silt and clay. The soil-to-plant transfer of radionuclides for each of these three texture fractions was analyzed. Lastly, the labile fraction was extracted from each textural part, and the activity concentration of the radionuclides (238)U and (226)Ra was measured. In order to assess the influence of soil texture on the soil-to-plant transfer process, we sought to identify possible correlations between the activity concentration in the plant compartment and those found in the different fractions within each soil compartment. The results showed that the soil-to-plant transfer process for uranium and radium depends on soil grain size, where the results for uranium showed a linear relationship between the activity concentration of uranium in the plant and the fine soil fraction. In contrast, a linear relation between the activity concentration of radium in the plant and the soil coarse-sand fraction was observed. Additionally, the presence of phosphate and calcium in the soil of all of the compartments studied affected the soil-to-plant transfer of uranium and radium, respectively.

  7. (234)U/(238)U signatures associated with uranium ore bodies: part 1 Ranger 3.

    PubMed

    Lowson, Richard T; McIntyre, Mark G

    2013-04-01

    The Ranger 3 ore body is an early Proterozoic U ore body in the Alligator Rivers U province, Northern Territory, Australia. It has surface expression with a redox front located between 30 and 50 m below the surface. The ground water U concentration and (234)U/(238)U AR signature in the top 10 m of the weathered zone are reported for 357 samples collected over 4 wet seasons, at 5 depths, along a transect in-line with the hydraulic gradient and along the centre line of the ore body and its associated dispersion halo. The results show that the weathered zone displays a general U isotope feature for this type of ore body with the (234)U/(238)U AR for the ground water and amorphous phase of the solid matrix being less than 1. The ground water (234)U/(238)U AR is independent of the annual monsoonal climate and depth within the range surface to 10 m. In the vicinity of the U ore body the ground water (234)U/(238)U AR is 0.75 and is very similar to the (234)U/(238)U AR of the amorphous phase of the solid (0.76). The (234)U/(238)U ARs of the amorphous phase and ground water rise and separate to values of 0.88 and 1.02 at the end of the transect. The rise and separation in (234)U/(238)U AR are interpreted as evidence that the source of the U in the ground water is from the water-soluble sub-phase of the amorphous phase and that the ground water flow is too fast to allow the processes occurring across the solid-water interface to reach chemical equilibrium. The data set is a robust characterisation of the coarse and fine detail of the (234)U/(238)U AR signature in the weathered zone of U ore bodies.

  8. (234)U/(238)U signatures associated with uranium ore bodies: part 3 Koongarra.

    PubMed

    Lowson, Richard T

    2013-04-01

    The Koongarra ore body is an early Proterozoic U ore body in the Alligator Rivers U province, Northern Territory, Australia. It has surface expression with a redox front located ∼30 m below the surface. The (234)U/(238)U activity ratios (AR) for the ground water and the amorphous phase of the solid have been analysed for the ore zone and dispersion halo as a function of depth. The results display a (234)U/(238)U AR signature with depth which may be common to all U ore bodies. The (234)U/(238)U AR is depressed below secular equilibrium in the weathered material above the redox front; rises significantly above secular equilibrium in the vicinity of the redox front; and is followed by a gradual decrease with depth below the redox front. The amplitude of the profile is a function of local conditions. A model is proposed for the signature in which oxidising waters preferentially leach the (234)U sites at the redox front due to preconditioning of the (234)U sites by α recoil during the decay of (23)(8)U to (23)(4)U. Mass balance requires the solid material left behind the redox front to have a (234)U/(238)U AR reduced below 1. Local second order effects may be superimposed on the signature. The signature may have application to calibrating scenarios for nuclear waste repositories, assisting in understanding historical climates, economic evaluation of U ore bodies and U exploration.

  9. Ocean mixing and ice-sheet control of seawater 234U/238U during the last deglaciation

    NASA Astrophysics Data System (ADS)

    Chen, Tianyu; Robinson, Laura F.; Beasley, Matthew P.; Claxton, Louis M.; Andersen, Morten B.; Gregoire, Lauren J.; Wadham, Jemma; Fornari, Daniel J.; Harpp, Karen S.

    2016-11-01

    Seawater 234U/238U provides global-scale information about continental weathering and is vital for marine uranium-series geochronology. Existing evidence supports an increase in 234U/238U since the last glacial period, but the timing and amplitude of its variability has been poorly constrained. Here we report two seawater 234U/238U records based on well-preserved deep-sea corals from the low-latitude Atlantic and Pacific Oceans. The Atlantic 234U/238U started to increase before major sea-level rise and overshot the modern value by 3 per mil during the early deglaciation. Deglacial 234U/238U in the Pacific converged with that in the Atlantic after the abrupt resumption of Atlantic meridional overturning. We suggest that ocean mixing and early deglacial release of excess 234U from enhanced subglacial melting of the Northern Hemisphere ice sheets have driven the observed 234U/238U evolution.

  10. (234)U/(238)U signatures associated with uranium ore bodies: part 2 Manyingee.

    PubMed

    Lowson, Richard T; McIntyre, Mark G

    2013-04-01

    The Manyingee ore body is a roll-front U ore body located at depth in the Cretaceous sandstone sediments of a Proterozoic palaeo valley. It is located in a confined aquifer. The aquifer is recharged 4 km upstream by the Ashburton River. Groundwater samples were collected at and up to 4.7 km downstream of the ore body. The ground water (234)U/(238)U activity ratios (AR) were elevated to 1.86 in the vicinity of the ore body and then declined to 1.06 over the 4.7 km transect. The elevated (234)U/(238)U ARs are attributed to selective leaching of (234)U sites by oxidising waters, with α recoil as a necessary precursor to produce activated (234)U sites. Direct ejection into another phase following α recoil is considered to be a minor contributor to (234)U -(238)U disequilibrium in this environment. The profile is considered to be typical of the (234)U/(238)U AR profile at and down gradient of the redox front of a U ore body.

  11. Field analyses of (238)U and (226)Ra in two uranium mill tailings piles from Niger using portable HPGe detector.

    PubMed

    Déjeant, Adrien; Bourva, Ludovic; Sia, Radia; Galoisy, Laurence; Calas, Georges; Phrommavanh, Vannapha; Descostes, Michael

    2014-11-01

    The radioactivities of (238)U and (226)Ra in mill tailings from the U mines of COMINAK and SOMAÏR in Niger were measured and quantified using a portable High-Purity Germanium (HPGe) detector. The (238)U and (226)Ra activities were measured under field conditions on drilling cores with 600s measurements and without any sample preparation. Field results were compared with those obtained by Inductive Coupled Plasma Atomic Emission Spectroscopy (ICP-AES) and emanometry techniques. This comparison indicates that gamma-ray absorption by such geological samples does not cause significant deviations. This work shows the feasibility of using portable HPGe detector in the field as a preliminary method to observe variations of radionuclides concentration with the aim of identifying samples of interest. The HPGe is particularly useful for samples with strong secular disequilibrium such as mill tailings.

  12. /sup 238/U, /sup 226/Ra and /sup 210/Pb in some vent waters of the Galapagos spreading center

    SciTech Connect

    Krishnaswami, S.; Turekian, K.K.

    1982-08-01

    The concentrations of /sup 226/Ra, /sup 238/U and /sup 210/Pb have been measured in waters from the Mussel Bed and the Rose Garden thermal fields at the Galapagos spreading center over a temperature range of approx.2.5--16 /sup 0/C. The /sup 226/Ra-T plots yield slopes of 0.112 and 0.036 dpm/kg /sup 0/C for the Mussel Bed and the Rose Garden respectively yielding a global hydrothermal /sup 226/Ra flux less than 5% of that required to sustain the oceanic inventory. /sup 238/U concentration in waters <9 /sup 0/C is the same as that in ambient sea water whereas water hotter than approx.9 /sup 0/C shows a decreasing trend with temperature to zero /sup 238/U at approx.29 /sup 0/C. /sup 210/Pb concentration in Mussel Bed increases with temperature, and extrapolated to approx.350 /sup 0/C yields a /sup 210/Pb concentration considerably less than that expected from /sup 222/Rn decay and basalt alteration.

  13. Geochemistry of speleothem records from southern Illinois: Development of (234U)/(238U) as a proxy for paleoprecipitation

    USGS Publications Warehouse

    Zhou, Juanzuo; Lundstrom, C.C.; Fouke, B.; Panno, S.; Hackley, K.; Curry, B.

    2005-01-01

    Natural waters universally show fractionation of uranium series (U-series) parent-daughter pairs, with the disequilibrium between 234U and 238U (234U)/(238U) commonly used as a tracer of groundwater flow. Because speleothems provide a temporal record of geochemical variations in groundwater precipitating calcite, (234U)/(238U) variations in speleothems provide a unique method of investigating water-rock interaction processes over millennium time scales. We present high precision Thermal Ionization Mass Spectrometric (TIMS) U-series analyses of speleothems and drip waters from Fogelpole Cave in southern Illinois. Data from all speleothems from the cave show an inverse correlation between (234U)/(238U) and U concentration, following the pattern observed in groundwaters globally. Within a 65-cm-long stalagmite, concordant 234U-238 U-230Th and 235U-231Pa ages for 5 samples indicate accurate chronology from 78.5 ka to 30 ka. Notably, (234U)/(238U)o which differs from most speleothems by having (234U)/(238U)o <1, positively correlates with speleothem growth rate. We generalize this to the observation that speleothems globally show (234U)/ (238U)o deviating farther from secular equilibrium at lower growth rates and approaching secular equilibrium at higher grow rates. Based on the Fogelpole observations, we suggest that groundwater (234U)/(238U) is controlled by the U oxidation state, the U concentration of the water and the fluid velocity. A transport model whereby U-series nuclides react and exchange with mineral surfaces can reproduce the observed trend between growth rate and (234U)/(238U)o. Based on this result, we suggest that (234U)/(238U)o in speleothems may record changes in hydrologic flux with time and thus could provide a useful proxy for long term records of paleoprecipitation. ?? 2005 Elsevier B.V. All rights reserved.

  14. Reliability of using 238U/235U and 234U/238U ratios from alpha spectrometry as qualitative indicators of enriched uranium contamination.

    PubMed

    Minteer, Mark; Winkler, Paul; Wyatt, Bill; Moreland, Scott; Johnson, Jamie; Winters, Tim

    2007-05-01

    Alpha spectrometry is a commonly used technique for the measurement of uranium isotopes in environmental samples because it is widely available at a relatively low cost. For natural uranium the (234)U to (238)U activity ratio should be 1 and the (238)U to (235)U activity ratio should be 21.7. However, a lower (238)U to (235)U ratio is usually observed in alpha spectrometric analysis of environmental soil samples. This observation has led to the conclusion that soils from nuclear weapons facilities were contaminated with highly enriched uranium. This study was undertaken to test the reliability of using activity ratios from alpha spectrometry to infer the presence of highly enriched uranium in soil samples. The results of these experiments indicate that the (238)U to (235)U activity ratio is not a reliable indicator, but that the (234)U to (238)U activity ratio can be used to qualitatively indicate the presence of highly enriched uranium at concentrations near 10 ng g(-1) and above.

  15. Dating open systems by the 238U- 234U- 230Th method: application to Quaternary reef terraces

    NASA Astrophysics Data System (ADS)

    Villemant, B.; Feuillet, N.

    2003-05-01

    The sedimentation conditions and diagenetic processes of biogenic and inorganic carbonates are such that the assumptions of a closed system evolution and the absence of initial Th invoked in classical 238U- 234U- 230Th dating methods are very often not fulfilled for such material. This problem is of interest for all studies requiring accurate dating of corals or aragonite-rich sediments as in palaeoclimatology or neotectonics. Extending the approach of Henderson and Slowey [Nature 404 (2000) 61-66], we propose a consistent model that takes into account possible initial 230Th excess and where continuous selective redistribution (gain or loss) of 234U, 234Th and 230Th is controlled by recoil processes. This model applied to Quaternary marine terraces in Barbados, Marie Galante (Lesser Antilles arc) and Pacific islands, is able to explain the large scatter in isotopic compositions observed in the series of cogenetic corals or sediments. We show that recoil processes generally tend to increase the ( 234U/ 238U) and ( 230Th/ 234U) ratios with time, leading to an overestimation of the apparent ages calculated using classical methods. On the basis of simple assumptions (identical 'marine' initial ( 234U/ 238U) 0 and ( 230Th/ 232Th) 0 ratios), we propose a method for calculating a best estimate of the age of cogenetic series. Our model offers an alternative way to date old reef terraces where corals are almost systematically altered and where classical dating methods do not apply. It may also explain the apparent variations of the ( 234U/ 238U) seawater initial ratio estimated from corals formed in the last 300 ka and the apparent uncoupling between sea-level highstands and high-latitude Northern Hemisphere summer insolation. Our set of equations can be applied to all weathering processes where the mobility of U-series isotopes is controlled by recoil.

  16. Investigations on the activity concentrations of 238U, 226RA, 228RA, 210PB and 40K in Jordan phosphogypsum and fertilizers.

    PubMed

    Al-Jundi, J; Al-Ahmad, N; Shehadeh, H; Afaneh, F; Maghrabi, M; Gerstmann, U; Höllriegl, V; Oeh, U

    2008-01-01

    The activity concentrations of naturally occurring radionuclides ((238)U, (226)Ra, (228)Ra, (210)Pb and (40)K) in Jordanian phosphate ore, fertilizer material and phosphogypsum piles were investigated. The results show the partitioning of radionuclides in fertilizer products and phosphogypsum piles. The outcome of this study will enrich the Jordanian radiological map database, and will be useful for an estimation of the radiological impact of this industrial complex on the immediate environment. The activity concentration of (210)Pb was found to vary from 95 +/- 8 to 129 +/- 8 Bq kg(-1) with a mean value of 111 +/- 14 Bq kg(-1) in fertilizer samples, and from 364 +/- 8 to 428 +/- 10 Bq kg(-1) with a mean value of 391 +/- 30 Bq kg(-1) in phosphogypsum samples; while in phosphate wet rock samples, it was found to vary between 621 +/- 9 and 637 +/- 10 Bq kg(-1), with a mean value of 628 +/- 7 Bq kg(-1). The activity concentration of (226)Ra in fertilizer samples (between 31 +/- 4 and 42 +/- 5 Bq kg(-1) with a mean value of 37 +/- 6 Bq kg(-1)) was found to be much smaller than the activity concentration of (226)Ra in phosphogypsum samples (between 302 +/- 8 and 442 +/- 8 Bq kg(-1) with a mean value of 376 +/- 62 Bq kg(-1)). In contrast, the activity concentration of (238)U in fertilizer samples (between 1011 +/- 13 and 1061 +/- 14 Bq kg(-1) with a mean value of 1033 +/- 22 Bq kg(-1)) was found to be much higher than the activity concentration of (238)U in phosphogypsum samples (between 14 +/- 5 and 37 +/- 7 Bq kg(-1) with a mean value of 22 +/- 11 Bq kg(-1)). This indicates that (210)Pb and (226)Ra show similar behaviour, and are concentrated in phosphogypsum piles. In addition, both isotopes enhanced the activity concentration in phosphogypsum piles, while (238)U enhanced the activity concentration in the fertilizer. Due to the radioactivity released from the phosphate rock processing plants into the environment, the highest collective dose commitment for the lungs

  17. The cumulative effect of three decades of phosphogypsum amendments in reclaimed marsh soils from SW Spain: (226)Ra, (238)U and Cd contents in soils and tomato fruit.

    PubMed

    Abril, José-María; García-Tenorio, Rafael; Enamorado, Santiago M; Hurtado, M Dolores; Andreu, Luis; Delgado, Antonio

    2008-09-15

    Phosphogypsum (PG), a by-product of the phosphate fertiliser industries, has been applied as soil amendment to reduce Na saturation in soils, as in the reclaimed marsh area from SW Spain, where available PG has a typical fingerprint of 710+/-40 Bq kg(-1) of (226)Ra, 165+/-15 Bq kg(-1) of (238)U and 2.8+/-0.4 mg kg(-1) of Cd. This work was focussed on the cumulative effects of PG amendments on the enrichment of these pollutants in cultivated soils and plants (Lycopersicum esculentum Mill L.) from the area studied, where PG has been applied since 1978 at recommended rates of 20-25 Mg ha(-1) every 2-3 years. A field experiment was conducted over three years to compare activity concentrations of (226)Ra ((214)Pb) and (238)U ((234)Th) in non-reclaimed soils, reclaimed soils with no additional PG application, and reclaimed soils with two additional PG applications. A non-significant effect of two PG amendments (in three years) was observed when compared with non-amended reclaimed plots. Nevertheless, a significant (p<0.05) enrichment of (226)Ra was observed in the surface horizon (0-30 cm) of reclaimed plots relative to deeper horizons and also when compared with the surface horizon of non-reclaimed soil (p<0.05), thereby revealing the cumulative effect of three decades of PG applications. Furthermore, the effect of a continuous application of PG was studied by analysing soils and tomato fruits from six commercial farms with different cumulative rates of PG applied. Cadmium concentrations in tomatoes, which were one order of magnitude higher than those found in tomatoes from other areas in South Spain, were positively correlated (r = 0.917) with (226)Ra-concentration in soils, which can be considered an accurate index of the cumulative PG rate of each farm.

  18. sup 234 U/ sup 238 U and sup 230 Th/ sup 234 U activity ratios in the collidal phases of aquifers in lateritic weathered zones

    SciTech Connect

    Short, S.A.; Lowson, R.T. ); Ellis, J. )

    1988-11-01

    A procedure was developed for comparing solute and colloid phases of groundwaters in contact with uranium ore bodies at Nabarlek and Koongarra in the Alligator Rivers region, Northern Territory, Australia. Single-pass ultrafiltration of large volumes with cut-offs of 18 nm and 1 {mu}m was used. Colloids were composed of Fe and Si species with sorbed U and U daughters. Uranium isotopes were mostly present as soluble species. Thorium was significantly associated with the colloids. The {sup 234}U/{sup 238}U activity ratios (ARs) were similar in solute and colloid phases close to the ore bodies but further down-gradient colloids were generally more depleted of {sup 234}U than the solute. The {sup 230}Th/{sup 234}U ARs rose from very low values for both solute and colloid phases close to the ore bodies through several orders of magnitude to much higher values further down-gradient. Colloid {sup 230}Th/{sup 234}U ARs were always significantly greater than solute ARs. Results were consistent with a systematic leaching of U from colloids going down-gradient and very little mobilization of ore body. {sup 230}Th relative to U. Ubiquitous complexes {sup 232}Th appeared to suppress the solubility of {sup 230}Th.

  19. 234U /238U and 230Th /234U activity ratios in the colloidal phases of aquifers in lateritic weathered zones

    NASA Astrophysics Data System (ADS)

    Short, Stephen A.; Lowson, Richard T.; Ellis, John

    1988-11-01

    A procedure was developed for comparing solute and colloid phases of groundwaters in contact with uranium ore bodies at Nabarlek and Koongarra in the Alligator Rivers region, Northern Territory, Australia. Single-pass ultrafiltration of large volumes with cut-offs of 18 nm and 1 μm was used. Colloids were composed of Fe and Si species with sorbed U and U daughters. Uranium isotopes were mostly present as soluble species. Thorium was significantly associated with the colloids. The 234U /238U activity ratios (ARs) were similar in solute and colloid phases close to the ore bodies but further down-gradient colloids were generally more depleted of 234U than the solute. The 230Th /234U ARs rose from very low values for both solute and colloid phases close to the ore bodies through several orders of magnitude to much higher values further down-gradient. Colloid 230Th /234U ARs were always significantly greater than solute ARs. Results were consistent with a systematic leaching of U from colloids going down-gradient and very little mobilization of ore-body 230Th relative to U. Ubiquitous complexed 232Th appeared to suppress the solubility of 230Th.

  20. Quantification of transfer of (238)U, (226)Ra, (232)Th, (40)K and (137)Cs in mosses of a semi-natural ecosystem.

    PubMed

    Dragović, S; Mihailović, N; Gajić, B

    2010-02-01

    There is a lack of appropriate data on transfer of some radionuclides on many terrestrial biota groups. To expand the available data concentration ratios of (238)U, (226)Ra, (232)Th, (40)K and (137)Cs in mosses are presented in this paper. The relationship between concentration ratios of radionuclides and physicochemical characteristics of the underlying soil was also investigated. The data on concentration ratios obtained here will provide a useful addition to the currently used database of transfer parameters, particularly for natural radionuclides.

  1. 234U/238U evidence for local recharge and patterns of groundwater flow in the vicinity of Yucca Mountain, Nevada, USA

    USGS Publications Warehouse

    Paces, J.B.; Ludwig, K. R.; Peterman, Z.E.; Neymark, L.A.

    2002-01-01

    Uranium concentrations and 234U/238U ratios in saturated-zone and perched ground water were used to investigate hydrologic flow and downgradient dilution and dispersion in the vicinity of Yucca Mountain, a potential high-level radioactive waste disposal site. The U data were obtained by thermal ionization mass spectrometry on more than 280 samples from the Death Valley regional flow system. Large variations in both U concentrations (commonly 0.6-10 ??g 1-1) and 234U/238U activity ratios (commonly 1.5-6) are present on both local and regional scales; however, ground water with 234U/238U activity ratios from 7 up to 8.06 is restricted largely to samples from Yucca Mountain. Data from ground water in the Tertiary volcanic and Quaternary alluvial aquifers at and adjacent to Yucca Mountain plot in 3 distinct fields of reciprocal U concentration versus 234U/238U activity ratio correlated to different geographic areas. Ground water to the west of Yucca Mountain has large U concentrations and moderate 234U/238U whereas ground water to the east in the Fortymile flow system has similar 234U/238U, but distinctly smaller U concentrations. Ground water beneath the central part of Yucca Mountain has intermediate U concentrations but distinctive 234U/238U activity ratios of about 7-8. Perched water from the lower part of the unsaturated zone at Yucca Mountain has similarly large values of 234U/238U. These U data imply that the Tertiary volcanic aquifer beneath the central part of Yucca Mountain is isolated from north-south regional flow. The similarity of 234U/238U in both saturated- and unsaturated-zone ground water at Yucca Mountain further indicates that saturated-zone ground water beneath Yucca Mountain is dominated by local recharge rather than regional flow. The distinctive 234U/238U signatures also provide a natural tracer of downgradient flow. Elevated 234U/238U in ground water from two water-supply wells east of Yucca Mountain are interpreted as the result of induced

  2. Testing the 234U/238U weathering tracer in a tropical granitoid watershed, Luquillo, Puerto Rico

    NASA Astrophysics Data System (ADS)

    Pett-Ridge, J. C.; Derry, L. A.

    2006-12-01

    Recent studies have employed U-series disequilibria as a tracer of both weathering profile development and of timescale of erosion for whole watersheds. We have undertaken a detailed analysis of the behavior of the U- series isotopes in a previously well-characterized watershed in order to test this approach. In the Rio Icacos watershed in the Luquillo Mountains of Puerto Rico, previous studies have determined both the rate of propagation of the chemical weathering front by regolith mass balance analysis, and the surface denudation rate using the cosmogenic 10Be tracer. Our study aims to determine whether the U-series approach provides regolith development and erosion rates in agreement with those previously determined. In order to better constrain interpretations based on U-series data, we have coupled the U-series analysis with analyses of trace element concentrations, δ^{30}Si, Ge/Si, and 87Sr/86Sr ratios. Used together, these geochemical tracers provide a powerful tool for understanding weathering reactions, chemical transfers within and out of the weathering profile, and the timing of these chemical transfers. Analyses of soil, saprolite and pore water samples reveal a complex history of U and Th transformations including mobilization of both U and Th in the soil followed by re-adsorption deeper in the profile. 234U/238U activity ratios in soil and saprolite show significant variability both with depth, and also among individual mineral phases at any particular depth. This variation among mineral phases, combined with the likely physical sorting of these phases during erosional transport, results in an additional isotopic fractionation unrelated to that imparted by the weathering process. This implies that suspended sediment samples taken from streamwater are unlikely to accurately reflect the average disequilibria carried by the secondary minerals phases in the soil and saprolite. Our analyses also reveal a significant contribution of atmospheric mineral

  3. IUPAC-IUGS status report on the half-lives of 238U, 235U and 234U

    NASA Astrophysics Data System (ADS)

    Villa, I. M.; Bonardi, M. L.; De Bièvre, P.; Holden, N. E.; Renne, P. R.

    2016-01-01

    The current state of knowledge on the half-lives of the long-lived U radionuclides has been reviewed by the IUPAC-IUGS joint Task Group "Isotopes in Geosciences". 238U is assigned a half-life of (4.4683 ± 0.0096) Ga, i.e. a decay constant λ238 = (0.155125 ± 0.000333) Ga-1. The coverage factor is k = 2 for this and all other estimates presented here. The 238U half-life can be used as a reference for the half-lives/decay constants of all other isotopic geochronometers. A revision of the half-life of 235U based on intercomparison of natural geological samples is premature. The improved repeatability of mass spectrometric measurements has revealed Type B uncertainties that had been dismissed as subordinate in the past. The combined uncertainty of these as yet incompletely charted and quantified sources of Type B uncertainty may be no smaller than the currently accepted uncertainty of the α counting experiments. A provisional value for the 234U half-life can be calculated with the assumption of secular equilibrium in the analyzed natural samples. This assumption has not yet been verified independently and its metrological traceability appears sub-optimum. A Type B evaluation suggests that the ca. 0.17% offset between the N(234U)/N(238U) number-ratios of the natural samples used to estimate the 235U half-life and those of the four samples used to estimate the 234U half-life should be compounded into the standard measurement uncertainty of the latter. The resulting provisional uncertainty interval (k = 2) for the 234U half-life is (244.55-247.77) ka, corresponding to λ234 = (2.8203-2.8344) Ma-1.

  4. 206Pb-230Th-234U-238U and 207Pb-235U geochronology of Quaternary opal, Yucca Mountain, Nevada

    USGS Publications Warehouse

    Neymark, Leonid A.; Amelin, Yuri V.; Paces, James B.

    2000-01-01

    U–Th–Pb isotopic systems have been studied in submillimeter-thick outermost layers of Quaternary opal occurring in calcite–silica fracture and cavity coatings within Tertiary tuffs at Yucca Mountain, Nevada, USA. These coatings preserve a record of paleohydrologic conditions at this site, which is being evaluated as a potential high-level nuclear waste repository. The opal precipitated from groundwater is variably enriched in 234U (measured 234U/238U activity ratio 1.124–6.179) and has high U (30–313 ppm), low Th (0.008–3.7 ppm), and low common Pb concentrations (measured 206Pb/204Pb up to 11,370). It has been demonstrated that the laboratory acid treatment used in this study to clean sample surfaces and to remove adherent calcite, did not disturb U–Th–Pb isotopic systems in opal. The opal ages calculated from 206Pb∗/238U and 207Pb∗/235U ratios display strong reverse discordance because of excess radiogenic 206Pb∗ derived from the elevated initial 234U. The data are best interpreted using projections of a new four-dimensional concordia diagram defined by 206Pb∗/238U, 207Pb∗/235U, 234U/238Uactivity, and 230Th/238Uactivity. Ages and initial 234U/238U activity ratios have been calculated using different projections of this diagram and tested for concordance. The data are discordant, that is observed 207Pb∗/235U ages of 170 ± 32 (2σ) to 1772 ± 40 ka are systematically older than 230Th/U ages of 34.1 ± 0.6 to 452 ± 32 ka. The age discordance is not a result of migration of uranium and its decay products under the open system conditions, but a consequence of noninstantaneous growth of opal. Combined U–Pb and 230Th/U ages support the model of slow mineral deposition at the rates of millimeters per million years resulting in layering on a scale too fine for mechanical sampling. In this case, U–Pb ages provide more accurate estimates of the average age for mixed multiage samples than 230Th/U ages, because ages based on shorter

  5. Extensive radioactive characterization of a phosphogypsum stack in SW Spain: 226Ra, 238U, 210Po concentrations and 222Rn exhalation rate.

    PubMed

    Abril, José-María; García-Tenorio, Rafael; Manjón, Guillermo

    2009-05-30

    Phosphogypsum (PG) is a by-product of the phosphate fertilizer industries that contains relatively high concentrations of uranium series radionuclides. The US-EPA regulates the agriculture use of PG, attending to its (226)Ra content and to the (222)Rn exhalation rate from inactive stacks. Measurements of (222)Rn exhalation rates in PG stacks typically show a large and still poorly understood spatial and temporal variability, and the published data are scarce. This work studies an inactive PG stack in SW Spain of about 0.5 km(2) from where PG can be extracted for agriculture uses, and an agriculture soil 75 km apart, being representative of the farms to be amended with PG. Activity concentrations of (226)Ra, (238)U and (210)Po have been measured in 30 PG samples (0-90 cm horizon) allowing for the construction of maps with spatial distributions in the PG stack and for the characterization of the associated PG inputs to agriculture soils. Averaged (226)Ra concentrations for the stack were 730+/-60 Bq kg(-1) (d.w.), over the US-EPA limit of 370 Bq kg(-1). (222)Rn exhalation rate has been measured by the charcoal canister method in 49 sampling points with 3 canisters per sampling point. Values in PG stack were under the US-EPA limit of 2600 Bq m(-2)h(-1), but they were one order of magnitude higher than those found in the agriculture soil. Variability in radon emissions has been studied at different spatial scales. Radon exhalation rates were correlated with (226)Ra concentrations and daily potential evapotranspiration (ETo). They increased with ETo in agriculture soils, but showed an opposite behaviour in the PG stack.

  6. Uranium concentrations and 234U/238U activity ratios in fault-associated groundwater as possible earthquake precursors

    NASA Astrophysics Data System (ADS)

    Finkel, R. C.

    In order to assess the utility of uranium isotopes as fluid phase earthquake precursors, uranium concentrations and 234U/238U activity ratios have been monitored on a monthly or bimonthly basis in water from 24 wells and springs associated with Southern California fault zones. Uranium concentrations vary from 0.002 ppb at Indian Canyon Springs on the San Jacinto fault to 8.3 ppb at Lake Hughes well on the San Andreas fault in the Palmdale area. 234U/238U activity ratios vary from 0.88 at Agua Caliente Springs on the Elsinore fault to 5.4 at Niland Slab well on the San Andreas fault in the Imperial Valley. There was one large earthquake in the study area during 1979, the 15 October 1979 M=6.6 Imperial Valley earthquake. Correlated with this event, uranium concentrations varied by a factor of more than 60 and activity ratios by a factor of 3 at the Niland Slab site, about 70 km from the epicenter. At the other sites monitored, uranium concentrations varied in time, but with no apparent pattern, while uranium activity ratios remained essentially constant throughout the monitoring period.

  7. Crustal subsidence rate off Hawaii determined from sup 234 U/ sup 238 U ages of drowned coral reefs

    SciTech Connect

    Ludwig, K.R.; Szabo, B.J.; Simmons, K.R. ); Moore, J.G. )

    1991-02-01

    A series of submerged coral reefs off northwestern Hawaii was formed during (largely glacial) intervals when the rate of local sea-level rise was less than the maximum upward growth rate of the reefs. Mass-spectrometric {sup 234}U/{sup 238}U ages for samples from six such reefs range from 17 to 475 ka and indicate that this part of the Hawaiian Ridge has been subsiding at a roughly uniform rate of 2.6 mm/yr for the past 475 ka. The {sup 234}U/{sup 238}U ages are in general agreement with model ages of reef drowning (based on estimates of paleo-sea-level stands derived from oxygen-isotope ratios of deep-sea sediments), but there are disagreements in detail. The high attainable precision ({plus minus}10 ka or better on samples younger than {approximately}800 ka), large applicable age range, relative robustness against open-system behavior, and ease of analysis for this technique hold great promise for future applications of dating of 50-1,000 ka coral.

  8. Measurements of /sup 234/U, /sup 238/U and /sup 230/Th in excreta of uranium-mill crushermen

    SciTech Connect

    Fisher, D.R.; Jackson, P.O.; Brodacynski, G.G.; Scherpelz, R.I.

    1982-07-01

    Uranium and thorium levels in excreta of uranium mill crushermen who are routinely exposed to airborne uranium ore dust were measured. The purpose was to determine whether /sup 230/Th was preferentially retained over either /sup 234/U or /sup 238/U in the body. Urine and fecal samples were obtained from fourteen active crushermen with long histories of exposure to uranium ore dust, plus four retired crushermen and three control individuals for comparison. Radiochemical procedures were used to separate out the uranium and thorium fractions, which were then electroplated on stainless steel discs and assayed by alpha spectrometry. Significantly greater activity levels of /sup 234/U and /sup 238/U were measured in both urine and fecal samples obtained from uranium mill crushermen, indicating that uranium in the inhaled ore dust was cleared from the body with a shorter biological half-time than the daughter product /sup 230/Th. The measurements also indicated that uranium and thorium separate in vivo and have distinctly different metabolic pathways and transfer rates in the body. The appropriateness of current ICRP retention and clearance parameters for /sup 230/Th in ore dust is questioned.

  9. Coupling groundwater residence time and 234U/238U isotopic ratios in a granitic catchment (Vosges, Eastern France)

    NASA Astrophysics Data System (ADS)

    Viville, Daniel; Aquilina, Luc; Ackerer, Julien; Chatton, Eliot; Labasque, Thierry; Pierret, Marie-Claire; Granet, Mathieu; Perrone, Thierry; Chabaux, François

    2016-04-01

    Weathering processes are active in surface waters but groundwater also represents no neglectable chemical fluxes. As residence-time in groundwater are high, silicate weathering might take place and control Si, Ca and C fluxes. Weathering processes can be deduced from U isotopic ratios but the kinetics of these processes remain relatively poorly constrained. In order to better characterize these processes, we have coupled residence-times deduced from anthropogenic gases (CFC and SF6) analysis and 234U/238U isotopic ratios determination. Samples were collected in the Strengbach catchment (Hydro-geochemical Observatory OHGE, Vosges, eastern France). Two campaigns were carried out in May and August 2015 during two highly contrasted hydro-climatic periods. Both springs and boreholes down to 80 m depth have been sampled. A very clear geochemical distinction is observed between groundwater from surface springs and deeper groundwater from boreholes. Springs show much lower residence-time (few years) and specific chemical composition. Deeper groundwater have residence-time of several decades and different geochemical composition. A clear SF6 production is observed with increasing SF6 concentrations with residence-time. The campaign of May is characterized by highly groundwater levels and spring fluxes. All groundwater show very low residence time, except in the boreholes at depth greater than 40 m. Conversely, during low groundwater-level period in August, the residence times are much higher and CFC concentrations indicate a large mixing process between surface groundwater and deeper levels. The 234U/238U isotopic ratios confirm this vertical zonation in the boreholes, with much higher activity ratios in the deep ground-waters from borehole than in the surface and spring waters; Such high U activity ratios are indicative of long water-rock interactions, which is consistent with the long residence times deducted from the CFC and SF6 data.

  10. 234U and 238U concentration in brine from geopressured aquifers of the northern Gulf of Mexico basin

    USGS Publications Warehouse

    Kraemer, T.F.

    1981-01-01

    The 234U and 238U concentration in brine from six Gulf Coast geopressured aquifers has been determined. The results reveal very low uranium concentrations (from 0.003 to 0.03 ??g/l) and uranium activity ratios slightly greater than unity (from 1.06 to 1.62). Reducing conditions within the aquifers are responsible for the low uranium concentrations. The uranium activity ratios observed are well below those calculated using theoretical considerations of alpha-particle recoil effects. This can be explained by interference with alpha-recoil nuclides entering the liquid phase as a result of quartz overgrowths on sand grains and high-temperature re-equilibration that tends to minimize the effects of the alpha-recoil process. The fact that the uranium activity ratios of the brines are slightly greater than unity instead of the equilibrium value of 1.000 indicates that either the alpha particle recoil blocking and re-equlibration effects are not complete or that another process is operative that enriches the fluid in excess 234U by selectively removing uranium from radiation induced damage sites in the mineral (sand grain) matrix. ?? 1981.

  11. Chemical fertilizers as a source of (238)U, (40)K, (226)Ra, (222)Rn, and trace metal pollutant of the environment in Saudi Arabia.

    PubMed

    Alshahri, Fatimh; Alqahtani, Muna

    2015-06-01

    The specific activities of (238)U, (226)Ra, (40)K, and (222)Rn in chemical fertilizers were measured using gamma ray spectrometer and Cr-39 detector. In this study, 21 chemical fertilizers were collected from Eastern Saudi Arabian markets. The specific activities of (238)U ranged from 23 ± 0.5 to 3900 ± 195 Bq kg(-1); (226)Ra ranged from 5.60 ± 2.80 to 392 ± 18 Bq kg(-1); and (40)K ranged from 18.4 ± 3 to 16,476 ± 820 Bq kg(-1). The radon concentrations and the radon exhalation rates were found to vary from 3.20 ± 1.20 to 1532 ± 160 Bq m(-3) and from 1.60 to 774 mBq m(-2) h(-1), respectively. Radium equivalent activities (Raeq) were calculated for the analyzed samples to assess the radiation hazards arising due to the use of these chemical fertilizers in the agriculture soil. The Raeq for six local samples (nitrogen, phosphorous, and potassium (NPK) and single superphosphate (SSP)) and one imported sample (Sulfate of Potash (SOP)) were greater than the acceptable value 370 Bq kg(-1). The total air absorbed doses rates in air 1 m above the ground (D) were calculated for all samples. All samples, except one imported granule sample diammonium phosphate (DAP), were higher than the estimated average global terrestrial radiation of 55 nGy h(-1). The highest annual effective dose was in triple super phosphate (TSP) fertilizers (2.1 mSv y(-1)). The results show that the local TSP, imported SOP, and local NPK (sample 13) fertilizers were unacceptable for use as fertilizers in agricultural soil. Furthermore, the toxic elements and trace metals (Pb, Cd, Cr, Co, Ni, Hg, and As) were determined using atomic absorption spectrometer. The concentrations of chromium in chemical fertilizers were higher than the global values.

  12. 234U/238U isotope data from groundwater and solid-phase leachate samples near Tuba City Open Dump, Tuba City, Arizona

    USGS Publications Warehouse

    Johnson, Raymond H.; Horton, Robert J.; Otton, James K.; Ketterer, Michael K.

    2012-01-01

    This report releases 234U/238U isotope data, expressed as activity ratios, and uranium concentration data from analyses completed at Northern Arizona University for groundwater and solid-phase leachate samples that were collected in and around Tuba City Open Dump, Tuba City, Arizona, in 2008.

  13. 238U-234U-230Th disequilibrium in hydrogenous oceanic Fe-Mn crusts: Palaeoceanographic record or diagenetic alteration?

    USGS Publications Warehouse

    Chabaux, F.; O'Nions, R. K.; Cohen, A.S.; Hein, J.R.

    1997-01-01

    A detailed TIMS study of (234Uexc/238U), (230Th/232Th), and Th/U ratios have been performed on the outermost margin of ten hydrogenous Fe-Mn crusts from the equatorial Pacific Ocean and west-central Indian Ocean. Th/U concentration ratios generally decrease from the crust's surface down to 0.5-1 mm depth and growth rates estimated by uranium and thorium isotope ratios are significantly different in Fe-Mn crusts from the Peru Basin and the west-central Indian Ocean. Fe-Mn crusts from the same geographical area define a single trend in plots of Ln (234Uexc/238U) vs. Ln(230Th/232Th) and Th/U ratios vs. age of the analysed fractions. Results suggest that (1) hydrogenous Fe-Mn crusts remain closed-systems after formation, and consequently (2) the discrepancy observed between the 230Th and 234U chronometers in Fe-Mn crusts, and the variations of the Th/U ratios through the margin of Fe-Mn crusts, are not due to redistribution of uranium and thorium isotopes after oxyhydroxide precipitation, but rather to temporal variations of both Th/U and initial thorium activity ratios recorded by the Fe-Mn layers. Implications of these observations for determination of Fe-Mn crust growth-rates are discussed. Variations of both Th/U and initial Th activity ratios in Fe-Mn crusts might be related to changes in particle input to seawater and/or changes in ocean circulation during the last 150 ka. Copyright ?? 1997 Elsevier Science Ltd.

  14. Uranium ((234)U, (235)U and (238)U) contamination of the environment surrounding phosphogypsum waste heap in Wiślinka (northern Poland).

    PubMed

    Olszewski, Grzegorz; Boryło, Alicja; Skwarzec, Bogdan

    2015-08-01

    The aim of this work was to determine the uranium concentration ((234)U, (235)U and (238)U) and values of the activity ratio (234)U/(238)U in soil samples collected near phosphogypsum waste heap in Wiślinka (northern Poland). On the basis of the studies it was found that the values of the (234)U/(238)U activity ratio in the analyzed soils collected in the vicinity of phosphogypsum dump in Wiślinka are in most cases close to one and indicate the phosphogypsum origin of the analyzed nuclides. The obtained results of uranium concentrations are however much lower than in previous years before closing of the phosphogypsum stockpile. After this process and covering the phosphogypsum stockpile in Wiślinka with sewage sludge, phosphogypsum particles are successfully immobilized. In the light of the results the use of phosphate fertilizers seems to be a major problem. Prolonged and heavy rains can cause leaching accumulated uranium isotopes in the phosphogypsum stockpile, which will be washed into the Martwa Wisła and on the fields in the immediate vicinity of this storage.

  15. A study on possible use of Urtica dioica (common nettle) plants as uranium ((234)U, (238)U) contamination bioindicator near phosphogypsum stockpile.

    PubMed

    Olszewski, Grzegorz; Boryło, Alicja; Skwarzec, Bogdan

    The aim of this study was to determine uranium concentrations in common nettle (Urtica dioica) plants and corresponding soils samples which were collected from the area of phosphogypsum stockpile in Wiślinka (northern Poland). The uranium concentrations in roots depended on its concentrations in soils. Calculated BCF and TF values showed that soils characteristics and air deposition affect uranium absorption and that different uranium species have different affinities to U. dioica plants. The values of (234)U/(238)U activity ratio indicate natural origin of these radioisotopes in analyzed plants. Uranium concentration in plants roots is negatively weakly correlated with distance from phosphogypsum stockpile.

  16. Ingestion dose from 238U, 232Th, 226Ra, 40K and 137Cs in cereals, pulses and drinking water to adult population in a high background radiation area, Odisha, India.

    PubMed

    Lenka, Pradyumna; Sahoo, S K; Mohapatra, S; Patra, A C; Dubey, J S; Vidyasagar, D; Tripathi, R M; Puranik, V D

    2013-03-01

    A natural high background radiation area is located in Chhatrapur, Odisha in the eastern part of India. The inhabitants of this area are exposed to external radiation levels higher than the global average background values, due to the presence of uranium, thorium and its decay products in the monazite sands bearing placer deposits in its beaches. The concentrations of (232)Th, (238)U, (226)Ra, (40)K and (137)Cs were determined in cereals (rice and wheat), pulses and drinking water consumed by the population residing around this region and the corresponding annual ingestion dose was calculated. The annual ingestion doses from cereals, pulses and drinking water varied in the range of 109.4-936.8, 10.2-307.5 and 0.5-2.8 µSv y(-1), respectively. The estimated total annual average effective dose due to the ingestion of these radionuclides in cereals, pulses and drinking water was 530 µSv y(-1). The ingestion dose from cereals was the highest mainly due to a high consumption rate. The highest contribution of dose was found to be from (226)Ra for cereals and drinking water and (40)K was the major dose contributor from the intake of pulses. The contribution of man-made radionuclide (137)Cs to the total dose was found to be minimum. (226)Ra was found to be the largest contributor to ingestion dose from all sources.

  17. Uranium concentrations and /sup 234/U//sup 238/U activity ratios in fault-associated groundwater as possible earthquake precursors

    SciTech Connect

    Finkel, R.C.

    1981-05-01

    In order to assess the utility of uranium isotopes as fluid phase earthquake precursors, uranium concentrations and /sup 234/U//sup 238/U activity ratios have been monitored on a monthly or bimonthly basis in water from 24 wells and springs associated with Southern California fault zones. Uranium concentrations vary from 0.002 ppb at Indian Canyon Springs on the San Jacinto fault to 8.3 ppb at Lake Hughes well on the San Andreas fault in the Palmdale area. /sup 234/U//sup 238/U activity ratios vary from 0.88 at Agua Caliente Springs on the Elsinore fault to 5.4 at Niland Slab well on the San Andreas fault in the Imperial Valley. There was one large earthquake in the study area during 1979, the 15 October 1979 M = 6.6 Imperial Valley earthquake. Correlated with this event, uranium concentrations varied by a factor of more than 60 and activity ratios by a factor of 3 at the Niland Slab site, about 70 km from the epicenter. At the other sites monitored, uranium concentrations varied in time, but with no apparent pattern, while uranium activity ratios remained essentially constant throughout the monitoring period.

  18. Assessment of (226)Ra, (238)U, (232)Th, (137)Cs and (40)K activities from the northern coastline of Oman Sea (water and sediments).

    PubMed

    Darabi-Golestan, F; Hezarkhani, A; Zare, M R

    2017-02-27

    Water and sediment samples were collected from northern coast of Oman Sea covering from Goatr to Hormoz canyon seaport. Water and sediment quality assessment for naturally or anthropogenic radionuclides at Oman Sea as a main strategic golf for trade and transit, is an important issue. Correspondence analysis (CA) by R-mode analysis represents that sigma(T)-temperature-conductivity-O2 parameters are well-correlated with (226)Ra, (232)Th and (40)K. Accordingly Q-mode analysis revealed an indicator samples of ST13W for different radionuclides, ST03W for O2, and simultaneously ST34W-ST21W-ST08W-ST04W for sigma(T) parameters. The CA results overlapped with factor and cluster analysis results that explained 85.8% of total variance of water samples. Descriptive analysis of sediments indicates more significant variation than water samples. The (232)Th and (226)Ra generally showing that ST13D to ST25D sediments that restricted to Pi Bashk coastline are concentrated from (137)Cs and (40)K. By comparison with reference-values from Iran and other parts of the world, they are acceptable with respect to environmental and radioisotope hazards.

  19. Diagenesis of fossil coral skeletons: Correlation between trace elements, textures, and [sup 234]U/[sup 238]U

    SciTech Connect

    Bar-Matthews, M.; Wasserburg, G.J.; Chen, J.H. )

    1993-01-01

    A comparative study of Pleistocene fossil coral skeletons and of modern coral skeletons was carried out using petrographic and trace element analyses on a suite of Pleistocene samples that had previously been studied from [sup 234]U, [sup 230]Th, and U-[sup 230]Th ages (Chen et al. 1991). Evidence of a range of diagenetic changes can be recognized by optical (OM) and scanning electron microscopy (SEM). Using an electron microprobe and SEM, concentrations of Na, S, Sr, and Mg were measured. No other trace elements were detected. Na, S, and Mg contents of the matrix, the fibrous micropores, and radiating needles are highly variable and well correlated. High concentrations of Na, S, and Mg were found in modern living corals with lower concentrations in fossil corals and fibrous micropores, and the lowest value in the radiating needles. The reason for the correlations of Na, S, and Mg and crystal chemistry and the response to diagenesis of these trace elements is not understood. The average concentrations of Na, S, and Mg for each sample, when plotted against the whole coral initial [delta][sup 234]U, are generally correlated (Chen et al., 1991). As all these diagenetic changes involve the recystallization and deposition of aragonite, the authors infer that the geologic site of diagenesis both for forming the secondary aragonitic phases and for the enhancement of the [sup 234]U content in the fossil corals was the marine environment. It is possible that the textural and Na, S, and Mg trace element contents of fossil corals be used to ascertain the reliability of fossil coral skeletons for U-[sup 230]Th dating. The basic problem of identifying a priori unaltered coral skeletons for [sup 230]Th dating is not yet resolved. 64 refs., 16 figs., 5 tabs.

  20. 234U/238U Disequilibrium along stylolitic discontinuities in deep Mesozoic limestone formations of the Eastern Paris basin: evidence for discrete uranium mobility over the last 1-2 million years

    NASA Astrophysics Data System (ADS)

    Deschamps, P.; Hillaire-Marcel, C. E.; Michelot, J.-L.; Doucelance, R.; Ghaleb, B.; Buschaert, S.

    The (234U/238) equilibrium state of borehole core samples from the deep, low-permeability limestone formations surrounding the target argilite layer of the Meuse/Haute-Marne experimental site of the French agency for nuclear waste management -ANDRA- (Agence nationale pour la gestion des déchets radioactifs) was examined to improve understanding of naturally occurring radionuclide behaviour in such geological settings. Highly precise, accurate MC-ICP-MS measurements of the (234U/238U) activity ratio show that limestone samples characterised by pressure dissolution structures (stylolites or dissolution seams) display systematic (234U/238U) disequilibria, while the pristine carbonate samples remain in the secular equilibrium state. The systematic feature is observed throughout the zones marked by pressure dissolution structures: (i) the material within the seams shows a deficit of 234U over 238U ((234U/238U) down to 0.80) and (ii) the surrounding carbonate matrix is characterised by an activity ratio greater than unity (up to 1.05). These results highlight a centimetric-scale uranium remobilisation in the limestone formations along these sub-horizontal seams. Although their nature and modalities are not fully understood, the driving processes responsible for these disequilibria were active during the last 1-2 Ma.

  1. Porosity of the melting zone and variations in the solid mantle upwelling rate beneath Hawaii: Inferences from {sup 238}U-{sup 230}Th-{sup 226}Ra and {sup 235}U-{sup 231}Pa disequilibria

    SciTech Connect

    Sims, K.W.W.; DePaolo, D.J.; Murrell, M.T.; Baldridge, W.S.; Goldstein, S.; Clague, D.; Jull, M.

    1999-12-01

    Measurements of {sup 238}U-{sup 230}Th-{sup 226}Ra and {sup 235}U-{sup 231}Pa disequilibria in a suite of tholeiitic-to-basanitic lavas provide estimates of porosity, solid mantle upwelling rate and melt transport times beneath Hawaii. The observation that ({sup 230}Th/{sup 238}U) {gt} 1 indicates that garnet is required as a residual phase in the magma sources for all of the lavas. Both chromatographic porous flow and dynamic melting of a garnet peridotite source can adequately explain the combined U-Th-Ra and U-Pa data for these Hawaiian basalts. For chromatographic porous flow, the calculated maximum porosity in the melting zone ranges from 0.3--3% for tholeiites and 0.1--1% for alkali basalts and basanites, and solid mantle upwelling rates range from 40 to 100 cm/yr for tholeiites and from 1 to 3 cm/yr for basanites. For dynamic melting, the escape or threshold porosity is 0.5--2% for tholeiites and 0.1--0.8% for alkali basalts and basanites, and solid mantle upwelling rates range from 10 to 30 cm/yr for tholeiites and from 0.1 to 1 cm/yr for basanites. Assuming a constant melt productivity, calculated total melt fractions range from 15% for the tholeiitic basalts to 3% for alkali basalts and basanites.

  2. Developing 226Ra and 227Ac age-dating techniques for nuclear forensics to gain insight from concordant and non-concordant radiochronometers

    DOE PAGES

    Kayzar, Theresa M.; Williams, Ross W.

    2015-09-26

    The model age or ‘date of purification’ of a nuclear material is an important nuclear forensic signature. In this study, chemical separation and MC-ICP-MS measurement techniques were developed for 226 Ra and 227Ac: grand-daughter nuclides in the 238U and 235U decay chains respectively. The 230Th-234U, 226Ra-238U, 231Pa-235U, and 227Ac-235U radiochronometers were used to calculate model ages for CRM-U100 standard reference material and two highly-enriched pieces of uranium metal from the International Technical Working Group Round Robin 3 Exercise. In conclusion, the results demonstrate the accuracy of the 226Ra-238U and 227Ac-235U chronometers and provide information about nuclide migration during uranium processing.

  3. 234U/238U and δ87Sr in peat as tracers of paleosalinity in the Sacramento-San Joaquin Delta of California, USA

    USGS Publications Warehouse

    Drexler, Judith Z.; Paces, James B.; Alpers, Charles N.; Windham-Myers, Lisamarie; Neymark, Leonid; Bullen, Thomas D.; Taylor, Howard E.

    2013-01-01

    The purpose of this study was to determine the history of paleosalinity over the past 6000+ years in the Sacramento-San Joaquin Delta (the Delta), which is the innermost part of the San Francisco Estuary. We used a combination of Sr and U concentrations, d87Sr values, and 234U/238U activity ratios (AR) in peat as proxies for tracking paleosalinity. Peat cores were collected in marshes on Browns Island, Franks Wetland, and Bacon Channel Island in the Delta. Cores were dated using 137Cs, the onset of Pb and Hg contamination from hydraulic gold mining, and 14C. A proof of concept study showed that the dominant emergent macrophyte and major component of peat in the Delta, Schoenoplectus spp., incorporates Sr and U and that the isotopic composition of these elements tracks the ambient water salinity across the Estuary. Concentrations and isotopic compositions of Sr and U in the three main water sources contributing to the Delta (seawater, Sacramento River water, and San Joaquin River water) were used to construct a three-end-member mixing model. Delta paleosalinity was determined by examining variations in the distribution of peat samples through time within the area delineated by the mixing model. The Delta has long been considered a tidal freshwater marsh region, but only peat samples from Franks Wetland and Bacon Channel Island have shown a consistently fresh signal (<0.5 ppt) through time. Therefore, the eastern Delta, which occurs upstream from Bacon Channel Island along the San Joaquin River and its tributaries, has also been fresh for this time period. Over the past 6000+ years, the salinity regime at the western boundary of the Delta (Browns Island) has alternated between fresh and oligohaline (0.5-5 ppt).

  4. U-isotopes and (226)Ra as tracers of hydrogeochemical processes in carbonated karst aquifers from arid areas.

    PubMed

    Guerrero, José Luis; Vallejos, Ángela; Cerón, Juan Carlos; Sánchez-Martos, Francisco; Pulido-Bosch, Antonio; Bolívar, Juan Pedro

    2016-07-01

    Sierra de Gádor is a karst macrosystem with a highly complex geometry, located in southeastern Spain. In this arid environment, the main economic activities, agriculture and tourism, are supported by water resources from the Sierra de Gádor aquifer system. The aim of this work was to study the levels and behaviour of some of the most significant natural radionuclides in order to improve the knowledge of the hydrogeochemical processes involved in this groundwater system. For this study, 28 groundwater and 7 surface water samples were collected, and the activity concentrations of the natural U-isotopes ((238)U, (235)U and (234)U) and (226)Ra by alpha spectrometry were determined. The activity concentration of (238)U presented a large variation from around 1.1 to 65 mBq L(-1). Elevated groundwater U concentrations were the result of oxidising conditions that likely promoted U dissolution. The PHREEQC modelling code showed that dissolved U mainly existed as uranyl carbonate complexes. The (234)U/(238)U activity ratios were higher than unity for all samples (1.1-3.8). Additionally, these ratios were in greater disequilibrium in groundwater than surface water samples, the likely result of greater water-rock contact time. (226)Ra presented a wide range of activity concentrations, (0.8 up to about 4 × 10(2) mBq L(-1)); greatest concentrations were detected in the thermal area of Alhama. Most of the samples showed (226)Ra/(234)U activity ratios lower than unity (median = 0.3), likely the result of the greater mobility of U than Ra in the aquifer system. The natural U-isotopes concentrations were strongly correlated with dissolution of sulphate evaporites (mainly gypsum). (226)Ra had a more complex behaviour, showing a strong correlation with water salinity, which was particularly evident in locations where thermal anomalies were detected. The most saline samples showed the lowest (234)U/(238)U activity ratios, probably due to fast uniform bulk mineral dissolution

  5. Disequilibrium of the 238U series in basalt

    USGS Publications Warehouse

    Somayajulu, B.L.K.; Tatsumoto, M.; Rosholt, J.N.; Knight, R.J.

    1966-01-01

    Radioisotope analyses of basalt samples from Hawaii, Japan, and Iwo Jima show that: (1) 234U and 238U are virtually in radioactive equilibrium, (2) 230Th exceeds equilibrium values in all these samples, (3) 210Pb concentrations range from 10-200% of the equilibrium values and average 30% deficient, and (4) 226Ra is probably not in equilibrium with 234U. The source regions of the basalts or magma forming processes are open systems, chemically. The enrichment of some of the uranium-daughter nuclides is insufficient to account for the excess 206Pb in volcanic rocks. The isotopic composition of lead and specific activity of 210Pb in sublimates from Showa-shinzan, Japan are also reported. ?? 1966.

  6. Distribution of long-lived radionuclides of the 238U series in the sediments of a small river in a uranium mineralized region of Spain.

    PubMed

    Lozano, J C; Blanco Rodríguez, P; Tomé, F Vera

    2002-01-01

    A study is presented on the distribution and mobilization of the natural U isotopes (238U and 234U), 230Th, and 226Ra in the sediments of a small river crossing an uranium mineralized zone where a disused uranium mine is located. Due to the preferential directions for surface run-off waters and to the mine's situation, one sampling point along the river bed was identified as a point of accumulation of radionuclides. The average values of the activity concentrations (Bq/kg) in this sediment sample were 5,025, 5,055, 5,915 and 1,694 for 238U, 234U, 230Th and 226Ra, respectively, while the respective average values of the activity concentrations (Bq/kg) for the sediment sample considered to give the background level were 125, 124, 131 and 370. Isotopic ratios between the descendants of 238U served to clarify some paths of distribution, involving the soils nearest to the sampling points and the location of these points with respect to the disused mine. The differences in behaviour found between the uranium, thorium and radium isotopes were associated to the mobility of these radionuclides in the fluvial system studied. Correlations between the radionuclide activity concentration ratios and stable element concentrations in the sediment samples were also investigated.

  7. Fluxes of 238U decay series radionuclides in a dicalcium phosphate industrial plant.

    PubMed

    Casacuberta, N; Masqué, P; Garcia-Orellana, J

    2011-06-15

    The production of dicalcium phosphate (DCP) is part of the phosphate industry, which has been recently included in the positive list of the NORM industries defined in the revised version of the EU-BSS (Euratom 29/96). The objective of the present work is to study specific concentrations and fluxes of (238,234)U, (230)Th, (226)Ra, (210)Pb and (210)Po at the different stages of the DCP production. Results showed highest activities of (238)U and (210)Pb were found in DCP (1500-2000 Bq kg(-1)); (230)Th and (210)Po were released together with the sludges (1600-2000 Bq kg(-1)) and (226)Ra presented particularly high activities in water (48 × 10(3) Bq m(-3)) and in the reactor scales (115 × 10(3) Bq kg(-1)). Fluxes of radionuclides showed that (238)U outflows were equally distributed between sludges (16 × 10(3) kBq h(-1)) and dicalcium phosphate (20 × 10(3) kBq h(-1)); (230)Th and (210)Po were almost entirely released in the sludges (30 × 10(3)kBq h(-1)) and the greatest (210)Pb outflow was the DCP current (25 × 10(3) kBq h(-1)). (226)Ra was mainly discharged through the water effluent (12 × 10(3) kBq h(-1)). This work highlights the importance of studying the industrial processes involving NORM, as minor changes in the production steps lead to different radionuclide distribution in the process.

  8. sup 238 U- and sup 232 Th-series chronology of phonolite fractionation at Mount Erebus, Antarctica

    SciTech Connect

    Reagan, M.K. ); Volpe, A.M. ); Cashman, K.V. )

    1992-03-01

    Uranium, thorium, radium, and barium abundances and {sup 234}U/{sup 238}U and {sup 230}Th/{sup 232}Th isotopic ratios determined by thermal ionization mass spectrometry and ({sup 228}Th)/({sup 232}Th) activity ratios determined by alpha spectrometry are used to date anorthoclase growth and infer magma chamber residence times of phonolites erupted in 1984 and 1988 from Mount Erebus, Antarctica. The 1984 and 1988 glasses have slightly different ({sup 230}Th)/({sup 232}Th) ratios but both have a 10% excess of ({sup 230}Th) over ({sup 238}U) and equilibrium ({sup 228}Th) values. By comparing these data and Pb-isotopic data reported in SUN and HANSON (1975) to similar data for oceanic basalts, the duration of differentiation from basanite to phonolite is limited to less than 150,000 years. The anorthoclase separates have ({sup 230}Th)/({sup 238}U) ratios exceeding those of the associated glasses but have ({sup 230}Th)/({sup 232}Th) ratios like those of the glasses. Both glasses are depleted in {sup 226}Ra with respect to {sup 230}Th by about 25%, whereas associated anorthoclase separates have extreme excesses of {sup 226}Ra over {sup 230}Th and ({sup 228}Th)/({sup 232}Th) = 2.2. On a plot of ({sup 226}Ra)/Ba vs. ({sup 230}Th)/BA, the glass-anorthoclase pairs produce isochrons averaging 2,380 y, which represents the average age of anorthoclase growth in the shallow magma system at Erebus. The implied residence time of phonolite magmas in the shallow magma chamber system of Erebus is about 3,000 y. Final crystal growth occurred after intrusion into the convecting lava lake less than decades before eruption.

  9. Remeasurement of (234)U Half-Life.

    PubMed

    Varga, Zsolt; Nicholl, Adrian; Wallenius, Maria; Mayer, Klaus

    2016-03-01

    The half-life of (234)U has been measured using a novel approach. In this method, a uranium material was chemically purified from its thorium decay product at a well-known time. The ingrowth of the (230)Th daughter product in the material was followed by measuring the accumulated (230)Th daughter product relative to its parent (234)U nuclide using inductively coupled plasma mass spectrometry. Then, the (234)U decay constant and the respective half-life could be calculated using the radioactive decay equations based on the n((230)Th)/n((234)U) amount ratio. The obtained (234)U half-life is 244 900 ± 670 years (k = 1), which is in good agreement with the previously reported results in the literature with comparable uncertainty. The main advantages of the proposed method are that it does not require the assumption of secular equilibrium between (234)U and (238)U. Moreover, the calculation is independent from the (238)U half-life value and its uncertainty. The suggested methodology can also be applied for the remeasurement of the half-lives of several other long-lived radionuclides.

  10. (210)Pb-(226)Ra disequilibria in young gas-laden magmas.

    PubMed

    Reagan, Mark; Turner, Simon; Handley, Heather; Turner, Michael; Beier, Christoph; Caulfield, John; Peate, David

    2017-03-24

    We present new (238)U-(230)Th-(226)Ra-(210)Pb and supporting data for young lavas from southwest Pacific island arcs, Eyjafjallajökull, Iceland, and Terceira, Azores. The arc lavas have significant (238)U and (226)Ra excesses, whereas those from the ocean islands have moderate (230)Th and (226)Ra excesses, reflecting mantle melting in the presence of a water-rich fluid in the former and mantle melting by decompression in the latter. Differentiation to erupted compositions in both settings appears to have taken no longer than a few millennia. Variations in the ((210)Pb/(226)Ra)0 values in all settings largely result from degassing processes rather than mineral-melt partitioning. Like most other ocean island basalts, the Terceira basalt has a (210)Pb deficit, which we attribute to ~8.5 years of steady (222)Rn loss to a CO2-rich volatile phase while it traversed the crust. Lavas erupted from water-laden magma systems, including those investigated here, commonly have near equilibrium ((210)Pb/(226)Ra)0 values. Maintaining these equilibrium values requires minimal persistent loss or accumulation of (222)Rn in a gas phase. We infer that degassing during decompression of water-saturated magmas either causes these magmas to crystallize and stall in reservoirs where they reside under conditions of near stasis, or to quickly rise towards the surface and erupt.

  11. 210Pb-226Ra disequilibria in young gas-laden magmas

    NASA Astrophysics Data System (ADS)

    Reagan, Mark; Turner, Simon; Handley, Heather; Turner, Michael; Beier, Christoph; Caulfield, John; Peate, David

    2017-03-01

    We present new 238U-230Th-226Ra-210Pb and supporting data for young lavas from southwest Pacific island arcs, Eyjafjallajökull, Iceland, and Terceira, Azores. The arc lavas have significant 238U and 226Ra excesses, whereas those from the ocean islands have moderate 230Th and 226Ra excesses, reflecting mantle melting in the presence of a water-rich fluid in the former and mantle melting by decompression in the latter. Differentiation to erupted compositions in both settings appears to have taken no longer than a few millennia. Variations in the (210Pb/226Ra)0 values in all settings largely result from degassing processes rather than mineral-melt partitioning. Like most other ocean island basalts, the Terceira basalt has a 210Pb deficit, which we attribute to ~8.5 years of steady 222Rn loss to a CO2-rich volatile phase while it traversed the crust. Lavas erupted from water-laden magma systems, including those investigated here, commonly have near equilibrium (210Pb/226Ra)0 values. Maintaining these equilibrium values requires minimal persistent loss or accumulation of 222Rn in a gas phase. We infer that degassing during decompression of water-saturated magmas either causes these magmas to crystallize and stall in reservoirs where they reside under conditions of near stasis, or to quickly rise towards the surface and erupt.

  12. 210Pb-226Ra disequilibria in young gas-laden magmas

    PubMed Central

    Reagan, Mark; Turner, Simon; Handley, Heather; Turner, Michael; Beier, Christoph; Caulfield, John; Peate, David

    2017-01-01

    We present new 238U-230Th-226Ra-210Pb and supporting data for young lavas from southwest Pacific island arcs, Eyjafjallajökull, Iceland, and Terceira, Azores. The arc lavas have significant 238U and 226Ra excesses, whereas those from the ocean islands have moderate 230Th and 226Ra excesses, reflecting mantle melting in the presence of a water-rich fluid in the former and mantle melting by decompression in the latter. Differentiation to erupted compositions in both settings appears to have taken no longer than a few millennia. Variations in the (210Pb/226Ra)0 values in all settings largely result from degassing processes rather than mineral-melt partitioning. Like most other ocean island basalts, the Terceira basalt has a 210Pb deficit, which we attribute to ~8.5 years of steady 222Rn loss to a CO2-rich volatile phase while it traversed the crust. Lavas erupted from water-laden magma systems, including those investigated here, commonly have near equilibrium (210Pb/226Ra)0 values. Maintaining these equilibrium values requires minimal persistent loss or accumulation of 222Rn in a gas phase. We infer that degassing during decompression of water-saturated magmas either causes these magmas to crystallize and stall in reservoirs where they reside under conditions of near stasis, or to quickly rise towards the surface and erupt. PMID:28338093

  13. Radium isotopes ((226)Ra and (228)Ra) in Na-Cl type groundwaters from Tohoku District (Aomori, Akita and Yamagata Prefectures) in Japan.

    PubMed

    Tomita, Jumpei; Zhang, Jing; Yamamoto, Masayoshi

    2014-11-01

    A total of 28 Na-Cl type groundwater samples were collected from Aomori, Akita and Yamagata Prefectures, in the Tohoku District of Japan, and their radium isotope ((226)Ra and (228)Ra) concentrations were measured along with their chemical components and stable isotope ratios (δ(2)H and δ(18)Os). The (226)Ra concentrations in groundwater samples varied widely, ranging from 8.8 to 1587 mBq kg(-1). These concentrations showed an increasing tendency with the increase of the total dissolved solid (TDS) contents. The (228)Ra/(226)Ra activity ratios were in the range from 0.3 to 4.2, with most data being around 0.5-2. These ratios were within those of (232)Th/(238)U found in granitic and related rocks and so on in Japan, indicating that Ra isotopes mainly ejected into the groundwater by the alpha-recoil process. The relationship between (226)Ra and other parameters suggested that Ra isotopes in groundwater samples in this study were mainly constrained by adsorption-desorption reactions depending on salinity with wide variation. Clear correlation between (226)Ra-Ca, (226)Ra-Sr, (226)Ra-Ba and (226)Ra-TDS observed in sulfate-free groundwater samples indicated that Ra isotopes of them were constrained by adsorption-desorption reactions depending on salinity under reducing condition. In contrast, relationship of (226)Ra-Ca, (226)Ra-Sr, (226)Ra-Ba and (226)Ra-TDS in sulfate-containing groundwater samples varied widely, and then, removal or enhanced mobility of Ra isotopes of them were observed.

  14. 226Ra determination in phosphogypsum by alpha-particle spectrometry

    NASA Astrophysics Data System (ADS)

    Aguado, J. L.; Bolívar, J. P.; García-Tenorio, R.

    1999-01-01

    A radiochemical method for226Ra determination by alpha-particle spectrometry in environmental samples has been developed in our laboratory. The method has been validated by measurements in samples with known concentrations of this radionuclide and it has been applied in studies related to226Ra behaviour in phosphogypsum (the main by-product of producing phosphoric acid from phosphate rocks).

  15. Leaching of 226Ra from components of uranium mill tailings

    USGS Publications Warehouse

    Landa, E.R.

    1991-01-01

    A sequential extraction procedure was used to characterize the geochemical forms of 226Ra retained by mixtures of quartz sand and a variety of fine-grained rock and mineral species. These mixtures had previously been exposed to the sulfuric acid milling liquor of a simulated acid-leach uranium milling circuit. For most test cases, the major fraction of the 226Ra was extracted with 1 mol/1 NH4Cl and was deemed to be exchangeable. However, 226Ra retained by the barite-containing mixture was resistant to both 1 mol/1 NH4Cl and 1 mol/HCHCl extraction. ?? 1991.

  16. Concentration of {sup 226}Ra in human teeth

    SciTech Connect

    Yamamoto, Masayoishi; Ueno, Kaoru; Hinoide, Moriyo; Ohkubo, Yoshiteru

    1994-11-01

    {sup 226}Ra concentrations in human teeth from several cities, mainly Tokyo, Japan, were determined with emphasis on the measurement of low-level {sup 226}Ra by alpha-ray spectrometry following chemical separation. No appreciable differences in {sup 226}Ra concentration were found among various permanent teeth samples of different age groups in Tokyo. The mean {sup 226}Ra concentration for Tokyo was 0.51 {+-} 0.06 mBq (g CA){sup -1}. {sup 226}Ra concentration [mean: 0.67 {+-} 0.11 mBq (g Ca){sup -1}] in teeth in western regions of the country was statistically higher than that [mean: 0.48 {+-} 0.09 mBq (g Ca){sup -1}] in eastern ones. The mean {sup 226}Ra concentration [0.51 mBq (g CA){sup -1}] in teeth from Tokyo was less than the concentration [1.11 mBq (g CA){sup -1}] reported for vertebral bone samples of this city. 27 refs., 1 fig., 5 tabs.

  17. 226Ra and 228Ra in Iowa drinking water.

    PubMed

    Kriege, L B; Hahne, R M

    1982-10-01

    The University Hygienic Laboratory has been performing radiochemical analyses on drinking water in the state of Iowa for over 20 yr. Approximately one half of the 1250 community water supplies that exist in Iowa have been sampled roughly once every 3 yr for the past decade. Originally, raw and finished waters that showed a gross alpha activity of greater than or equal to 3.0 pCi/L were analyzed for 226Ra, but starting in July 1976, finished waters were analyzed for both 226Ra and 228Ra if the gross alpha activity was greater than or equal to 2.0 pCi/L. As of 10 June 1981, 604 community water supplies had submitted composited samples that have been analyzed for gross alpha, 226Ra, and 228Ra concentrations in compliance with the federal Safe Drinking Water Act (Public Law 93-523). Approximately 10% of these supplies were found to exceed the EPA-established maximum contaminant level (MCL) for 226Ra plus 228Ra of 5 pCi/L. The results revealed, consistent with several other investigators (Mc81; Mi80; Mic80), that some supplies had higher concentrations of 228Ra than of 226Ra. It was also concluded, in agreement with McCurdy and Mellor (Mc81), that some ground water samples cannot be accurately measured for gross alpha activity due to their high dissolved solids content.

  18. Rapid determination of 226Ra in emergency urine samples

    DOE PAGES

    Maxwell, Sherrod L.; Culligan, Brian K.; Hutchison, Jay B.; ...

    2014-02-27

    A new method has been developed at the Savannah River National Laboratory (SRNL) that can be used for the rapid determination of 226Ra in emergency urine samples following a radiological incident. If a radiological dispersive device event or a nuclear accident occurs, there will be an urgent need for rapid analyses of radionuclides in urine samples to ensure the safety of the public. Large numbers of urine samples will have to be analyzed very quickly. This new SRNL method was applied to 100 mL urine aliquots, however this method can be applied to smaller or larger sample aliquots as needed.more » The method was optimized for rapid turnaround times; urine samples may be prepared for counting in <3 h. A rapid calcium phosphate precipitation method was used to pre-concentrate 226Ra from the urine sample matrix, followed by removal of calcium by cation exchange separation. A stacked elution method using DGA Resin was used to purify the 226Ra during the cation exchange elution step. This approach combines the cation resin elution step with the simultaneous purification of 226Ra with DGA Resin, saving time. 133Ba was used instead of 225Ra as tracer to allow immediate counting; however, 225Ra can still be used as an option. The rapid purification of 226Ra to remove interferences using DGA Resin was compared with a slightly longer Ln Resin approach. A final barium sulfate micro-precipitation step was used with isopropanol present to reduce solubility; producing alpha spectrometry sources with peaks typically <40 keV FWHM (full width half max). This new rapid method is fast, has very high tracer yield (>90 %), and removes interferences effectively. The sample preparation method can also be adapted to ICP-MS measurement of 226Ra, with rapid removal of isobaric interferences.« less

  19. Metrological Determination of Natural Radioactive Isotopes {sup 226}Ra, {sup 228}Ra and {sup 210}Pb by Means of Ge Detector

    SciTech Connect

    Almeida, Maria Candida M. de; Delgado, Jose U.; Poledna, Roberto; Oliveira, Estela Maria de; Silva, Ronaldo L. da

    2008-08-07

    A metrological method to determine the activity per mass unity (activity concentration) of {sup 226}Ra and {sup 210}Pb ({sup 238}U decay series) and {sup 228}Ra ({sup 232}Th series) by gamma-ray spectrometers based on hyper-pure coaxial germanium detector was developed. In the soil the {sup 22}Ra (half-life = 1600 years) exhibits the same level of radioactivity as {sup 238}U (half-life 4.5x10{sup 9} years) because of a natural phenomenon called secular equilibrium. {sup 226}Ra decays into {sup 222}Rn (half-life = 3.8 days), a radioactive inert gas. After several days, the {sup 222}Rn naturally decays to {sup 218}Po (half-life = 3 minutes), where finally {sup 210}Pb (half-life = 22 years) is produced. The metrological capability of high-resolution gamma-ray spectrometry for naturally occurring radionuclides at environmental levels is showed, with emphasis on the use of 2 mL standard sources volume in a glass ampoule. Source preparation and calibration procedures are described. Radionuclide standards in an activity range of 10 to 250 Bq/g were produced which can be applied in a variety of environmental sample analysis (water, plant material, sediment, etc.). Uncertainties for {sup 226}Ra and {sup 210}Pb around 3% (k = 1) were obtained.

  20. Determination of 210Pb, 210Po, 226Ra, 228Ra and uranium isotopes in drinking water in order to comply with the requirements of the EU ‘Drinking Water Directive.

    PubMed

    Vasile, M; Loots, H; Jacobs, K; Verheyen, L; Sneyers, L; Verrezen, F; Bruggeman, M

    2016-03-01

    The European Union published in 2013 a new Drinking Water Directive with stricter requirements for measuring natural radioactivity. In order to adhere to this, a method for sequential separation of 210Pb, 210Po, 238U and 234U in drinking water was applied using UTEVA® and Sr resins. Polonium-210, 238U and 234U were quantified using alpha-particle spectrometry and 210Pb using liquid scintillation counting. Radium-226 and 228Ra were determined using 3M Empore Radium RAD Disks, and their quantification was done using a Quantulus™ 1220 liquid scintillation counter.

  1. (226Ra)/(230Th) Excess Generated in the Lower Crust: Implications for Magma Transport Rates in Arc Settings

    NASA Astrophysics Data System (ADS)

    Dufek, J. D.; Cooper, K. M.

    2004-12-01

    226Ra-excesses in arc magmas have been interpreted to result from flux melting of the mantle above subducting slabs and subsequent fast ascent rates of magma from slab to surface, up 1000 m/yr and higher. Implied by this hypothesis is that the magma has not stalled at any depth for long periods of time, limiting the amount of time for assimilation of crustal material and homogenization of magmas. However, mixing of mantle melts with mid to lower crustal melts has been inferred in numerous localities, especially in continental arc settings. In addition, very short residence times may be in conflict with crystal residence of thousands to tens of thousands of years in arc lavas. We present calculations that demonstrate that incongruent melting of the lower crust could either maintain or augment mantle-derived Ra-excesses and so reduce vertical transport rates to 10 m/yr or less. In particular, we found that dehydration melting of amphibolite can produce modeled 226Ra-excesses greater than 300 percent with corresponding 230Th-excesses of approx. 14 percent. Both the modal percentage of garnet and melt fraction contribute to the degree of Ra-excess, and a wide range of garnet compositions can produce significant disequilibria. Mixtures of such an amphibolite dehydration melt with mantle melts will likely retain a 238U-excess (subducted slab) signature, although lower crustal melting without such mixing could help explain some of the enigmatic silicic magmas observed that have 230Th-excesses. This amphibolite dehydration melting process will also produce elevated Sr/Y and La/Yb ratios, similar to those observed in several arc settings, that may distinguish these magmas from those with 226Ra-excesses produced by slab-dewatering alone.

  2. 226Ra or 226Ra/Ba dating of Holocene volcanic rocks: application to Mt. Etna and Merapi volcanoes

    NASA Astrophysics Data System (ADS)

    Condomines, M.; Gauthier, P. J.; Tanguy, J. C.; Gertisser, R.; Thouret, J. C.; Berthommier, P.; Camus, G.

    2005-02-01

    This paper shows how 226Ra- 230Th disequilibria can be used to date Holocene volcanic rocks from some well selected volcanoes. A systematic study of these disequilibria on historical or well-dated volcanic samples is indeed first required to test the applicability of this method. Two examples are described here to illustrate its potential. In the case of Mt. Etna, the good correlation observed between ( 226Ra) 0 activities at the time of eruption and Th contents in lava flows from the last two millennia [M. Condomines, J.C. Tanguy, V. Michaud, Magma dynamics at Mt. Etna: constraints from U-Th-Ra-Pb radioactive disequilibria and Sr isotopes in historical lavas, Earth Planet. Sci. Lett. 132 (1995) 25-41] is used to infer the ages of several newly analysed lava flows. The calculated ages are in good agreement with those deduced from the archaeomagnetic curve describing the variation of the geomagnetic field direction in southern Italy [J.C. Tanguy, I. Bucur, J.F.C. Thompson, Geomagnetic secular variation in Sicily and revised ages of historic lavas from Mt. Etna, Nature 318 (1985) 453-455, J.C. Tanguy, M. Le Goff, V. Chillemi, A. Paiotti, C. Principe, S. La Delfa, G. Patane, Variation séculaire de la direction du champ géomagnétique enregistrée par les laves de l'Etna et du Vésuve pendant les deux derniers millénaires, C. R. Acad. Sci. Paris 329 (1999) 557-564, J.C. Tanguy, M. Le Goff, C. Principe, S. Arrighi, V. Chillemi, A. Paiotti, S. La Delfa, G. Patane, Archaeomagnetic dating of Mediterranean volcanics of the last 2100 years: validity and limits. Earth Planet. Sci. Lett. 211 (2003) 111-124]. We also present a whole set of new U-series data on historical, recent, and older samples from Merapi (Indonesia), and show that the ( 226Ra)/Ba ratio has probably maintained a quasi-steady state value during at least the past four millennia, and can be used to infer the ( 226Ra) 0/Ba ratio of old volcanics at the time of eruption, and thus their ages. Comparison with

  3. Rapid method for the determination of 226Ra in hydraulic fracturing wastewater samples

    DOE PAGES

    Maxwell, Sherrod L.; Culligan, Brian K.; Warren, Richard A.; ...

    2016-03-24

    A new method that rapidly preconcentrates and measures 226Ra from hydraulic fracturing wastewater samples was developed in the Savannah River Environmental Laboratory. The method improves the quality of 226Ra measurements using gamma spectrometry by providing up to 100x preconcentration of 226Ra from this difficult sample matrix, which contains very high levels of calcium, barium, strontium, magnesium and sodium. The high chemical yield, typically 80-90%, facilitates a low detection limit, important for lower level samples, and indicates method ruggedness. Ba-133 tracer is used to determine chemical yield and correct for geometry-related counting issues. The 226Ra sample preparation takes < 2 hours.

  4. 230Th, 226Ra and 222Rn in abyssal sediments

    NASA Astrophysics Data System (ADS)

    Kadko, David

    1980-09-01

    A model that predicts the flux of 222Rn out of deep-sea sediment is presented. The radon is ultimately generated by 230Th which is stripped from the overlying water into the sediment. Data from many authors are compared with the model predictions. It is shown that the continental contribution of ionium is not significant, and that at low sedimentation rates, biological mixing and erosional processes strongly affect the surface concentration of the ionium. Two cores from areas of slow sediment accumulation, one from a manganese nodule region of the central Pacific and one from the Rio Grande Rise in the Atlantic were analyzed at closely spaced intervals for 230Th, 226Ra, and 210Pb. The Pacific core displayed evidence of biological mixing down to 12 cm and had a sedimentation rate of only 0.04 cm/kyr. The Atlantic core seemed to be mixed to 8 cm and had a sedimentation rate of 0.07 cm/kyr. Both cores had less total excess 230Th than predicted. Radium sediment profiles are generated from the 230Th model. Adsorbed, dissolved, and solid-phase radium is considered. According to the model, diffusional losses of radium are especially important at low sedimentation rates. Any particulate, or excess radium input is ignored in this model. The model fits the two analyzed cores if the fraction of total radium available for adsorption-desorption is about 0.5-0.7, and if K, the distribution coefficient, is about 1000. Finally, the flux of radon out of the sediments is derived from the model-generated radium profiles. It is shown that the resulting standing crop of 222Rn in the overlying water may be considered as an added constraint in budgeting 230Th and 226Ra in deep-sea sediments.

  5. A correlation between soil descriptions and {sup 226}Ra concentrations in Florida soils

    SciTech Connect

    Harrison, D.P.

    1992-12-31

    The soil radium content in Florida is highly variable. The range in radium concentrations, where the samples involved in this study are concerned, is from 0.1 pCi/g to 18.5 pCi/g. Low {sup 226}Ra concentrations (0.1 to 5 pCi/g) are evidenced in sands, moderate concentrations (5 to 11 pCi/g) are found in silt and gravel, and high {sup 226}Ra concentrations (>11 pCi/g) are found in soil horizons with shell, clay, and strata with phosphate. Strata containing phosphate yields a high concentration of {sup 226}Ra. The information obtained in this study, soil descriptions with their corresponding {sup 226}Ra concentrations, comes from geological cores drilled by geotechnical consultants with gamma spectrometry analysis performed by high resolution gamma spectroscopy. Concentration; of {sup 226}Ra generally increase with depth. These cores are usually terminated at 20 feet deep, with some cores being shallower than this due to hitting bedrock or encountering the water table. These frequency distributions give the core-logging geologist an approximate concentration of {sup 226}Ra based on the description of the soil. Since the correlation of {sup 226}Ra and soil descriptions can be used as a tool in assigning indoor radon potential, this study is of importance to land managers, contractors, developers, and regulating agencies who are attempting to place standards on tracts of land with {sup 226}Ra concentration used as a criterion.

  6. Leachable 226Ra in Philippine phosphogypsum and its implication in groundwater contamination in Isabel, Leyte, Philippines.

    PubMed

    Cañete, Socrates Jose P; Palad, Lorna Jean H; Enriquez, Eliza B; Garcia, Teofilo Y; Yulo-Nazarea, Teresa

    2008-07-01

    Phosphogypsum (PG), the major waste material in phosphate fertilizer processing, has been known to contain enhanced levels of naturally-occurring radionuclides especially (226)Ra. The lack of radioactivity data regarding Philippine phosphogypsum and its environmental behavior in the Philippine setting has brought concern on possible contamination of groundwater beneath the phosphogypsum ponds in Isabel, Leyte, Philippines. The radioactivity of Philippine phosphogypsum was determined and the leaching of (226)Ra from phosphogypsum and through local soil was quantified. Level of (226)Ra in groundwater samples in Isabel, Leyte, Philippines was also quantified to address the primary concern. It was found that the (226)Ra activity in Philippine phosphogypsum is distributed in a wide range from 91.5 to 935 Bq/kg. As much as 5% of (226)Ra can be leached from Philippine PG with deionized water. In vitro soil leach experiments suggest that the soil in the phosphate fertilizer plant area would be able to deter the intrusion of (226)Ra into the water table. Compared to reported values of natural groundwater levels of (226)Ra, the concentration of this radionuclide in Isabel, Leyte groundwater suggest that there is no (226)Ra intrusion brought about by the presence of phosphogypsum ponds in the area.

  7. 238,234U contents on Lepomis Cyanellus from San Marcos dam located in a uraniferous area

    NASA Astrophysics Data System (ADS)

    Lares, Magaly Cabral; Luna-Porres, Mayra Y.; Montero-Cabrera, María E.; Renteria-Villalobos, Marusia

    2014-07-01

    Fish species are suitable biomonitors of radioisotopes in aquatic systems. In the present study, it was made the determination of uranium isotopic contents on fish fillet (Lepomis Cyanellus) from San Marcos dam which is located in uranium mineralized zone. Uranium activity concentrations (AC) in fish samples were obtained on wet weight (ww), using liquid scintillation. 238U and 234U AC in fish fillet ranged from 0.0004 to 0.0167 Bq kg-1, and from 0.0013 to 0.0394 Bq kg-1, respectively. The activity ratio (234U/overflow="scroll">238U) in fish fillet ranged from 2.2 to 8.8. Lepomis cyanellus from San Marcos dam shows bioaccumulation factor (FB) of 0.6 L kg-1. The results suggest that the Lepomis Cyanellus in environments with high U contents tends to have a greater bioaccumulation compared to others.

  8. Age-dependent dose assessment of 226Ra from bottled water intake.

    PubMed

    Bronzovic, Maja; Marovic, Gordana

    2005-05-01

    Water may present a source of prolonged exposure to naturally occurring radionuclides. One of the most frequently occurring radionuclides in natural mineral and spring waters is 226Ra and its decay products. The contribution of drinking water to the total exposure is very small, at about 5% of the average effective dose attributable annually to natural background radiation, but that exposure contributes to the risk of adverse health consequences. In this study the mean values of 226Ra concentration determined in natural mineral and spring bottled waters range from 6 to 412 mBq L(-1), which is in accord with Croatian legislation. 226Ra effective doses per year from spring water consumption range up to 86 microSv, while 226Ra effective doses per year from mineral water consumption show much higher values. The highest 226Ra effective doses per year from mineral waters consumption, which are up to seven times higher than the dose recommended by WHO (100 microSv), were found in infants and teens. Based on this study, drinking of certain brands of bottled mineral water is not recommended for these age groups because assessed 226Ra effective doses per year exceed the recommended limits. From other research it is known that testosterone appears in elevated concentration during these life periods and affects bone calcification. Therefore, testosterone could affect the retention of 226Ra into the bone. To make more precise conclusions further research is necessary. Adults and especially elderly people are much less susceptible to the presence of 226Ra. According to the results obtained in this study, 226Ra effective doses per year assessed for these age groups were considerably lower (i.e., 10 microSv).

  9. Uranium isotope systematics of ferromanganese crusts in the Pacific Ocean: Implications for the marine 238U/235U isotope system

    NASA Astrophysics Data System (ADS)

    Goto, Kosuke T.; Anbar, Ariel D.; Gordon, Gwyneth W.; Romaniello, Stephen J.; Shimoda, Gen; Takaya, Yutaro; Tokumaru, Ayaka; Nozaki, Tatsuo; Suzuki, Katsuhiko; Machida, Shiki; Hanyu, Takeshi; Usui, Akira

    2014-12-01

    Variations of 238U/235U ratio (δ238U) in sedimentary rocks have been proposed as a possible proxy for the paleo-oceanic redox conditions, although the marine δ238U system is not fully understood. Here we investigate the spatial variation of δ238U in modern ferromanganese (Fe-Mn) crusts by analyzing U isotopes in the surface (0-3 mm depth) layer of 19 Fe-Mn crusts collected from 6 seamounts in the Pacific Ocean. δ238U values in the surface layers show little variation and range from -0.59‰ to -0.69‰. The uniformity of δ238U values is consistent with the long residence time of U in modern seawater, although the δ238U values are lighter than that of present-day seawater by ∼0.24‰. The light δ238U values are consistent with the isotope offset observed in previously reported adsorption experiment of U to Mn oxide. These results indicate that removal of U from seawater to Mn oxide is responsible for the second largest U isotope fractionation in the modern marine system, and could contribute to isotopically heavy U to seawater. Depth profiles of U isotopes (δ234U and δ238U) in two Fe-Mn crusts (MR12-03_D06-R01 and MC10_CB07_B), dated by Os isotope stratigraphy, were investigated to reconstruct the evolution of the oceanic redox state during the Cenozoic. The δ238U depth profiles show very limited ranges (-0.57‰ to -0.67‰ for MR12-03_D06-R01 and -0.56‰ to -0.69‰ for MC10_CB07_B), and have values that are similar to those of the surface layers of Fe-Mn crusts. The absence of any resolvable variation in the δ238U depth profiles may suggest that the relative amounts of oxic and reducing U sinks have not varied significantly over the past 45 Myr. However, the δ234U depth profiles of the same samples show evidence for the possible redistribution of 234U after deposition. Therefore, the depth profile of δ238U in Fe-Mn crusts may have been also overprinted by later chemical exchange with pore-water or seawater, and may not reflect the paleo

  10. Pygmy dipole response in 238U nucleus

    NASA Astrophysics Data System (ADS)

    Guliyev, Ekber; Kuliev, Ali Akbar; Quliyev, Huseynqulu

    2017-02-01

    The presence of the El pygmy dipole resonance (PDR) in the actinide nucleus 238U was shown via QRPA. Below the particle threshold energy, 24 excitation states were calculated. The calculations, is demonstrating the presence of a PDR with evidence for K splitting. The calculations further suggest that the PDR in 238U is predominantly K=0. The obtained results show universality of the PDR in atomic nuclei.

  11. Assessment of (226)Ra age-dependent dose from water intake.

    PubMed

    Porntepkasemsan, Boonsom; Srisuksawad, Kanitha

    2008-11-01

    The radioactivity in canal and ground waters collected in a 2-year long observation from the vicinity of the Rare Earth Research and Development Center (RRDC), Phathumthani Province, Thailand, was measured in order to determine the concentration of (226)Ra and to estimate the age-dependent effective dose to humans due to consumption. (226)Ra activities in both canal and ground waters were well below the WHO guidance level for drinking water quality of 1 Bq L(-1). The highest (226)Ra effective doses per year were found for infants and teens. However, the observed levels of calculated (226)Ra effective doses for all age groups in both canal and ground waters show satisfactory low values (less than 15 microSv yr(-1)). These values are acceptable in accordance with the WHO recommended reference dose level of 100 microSv yr(-1) from water intake of 2 Lday(-1).

  12. Measurement of 226Ra, 232Th, 137Cs and 40K activities of Wheat and Corn Products in Ilam Province – Iran and Resultant Annual Ingestion Radiation Dose

    PubMed Central

    CHANGIZI, Vahid; SHAFIEI, Elham; ZAREH, Mohammad Reza

    2013-01-01

    Background: Background: Natural background radiation is the main source of human exposure to radioactive material. Soils naturally have radioactive mineral contents. The aim of this study is to determine natural (238 U, 232 Th, 40 K) and artificial (137 Cs) radioactivity levels in wheat and corn fields of Eilam province. Methods: HPGe detector was used to measure the concentration activity of 238 U and 232 Th series, 40 K and 137 Cs in wheat and corn samples taken from different regions of Eilam province, in Iran. Results: In wheat and corn samples, the average activity concentrations of 226 Ra, 232 Th, 40 K and 137 Cs were found to be 1, 67, 0.5, 91.73, 0.01 and 0.81, 0.85, 101.52, 0.07 Bq/kg (dry weight), respectively. H ex and H in in the present work are lower than 1. The average value of H ex was found to be 0.02 and 0.025 and average value of H in to be found 0.025 and 0.027 in wheat fields samples and corn samples in Eilam provinces, respectively. The obtained values of AGDE are 30.49 mSv/yr for wheat filed samples and 37.89 mSv/yr for corn samples; the AEDE rate values are 5.28 mSv/yr in wheat filed samples and this average value was found to be 6.13 mSv/yr in corn samples in Eilam. Transfer factors (TFs) of long lived radionuclide such as 137 Cs, 226 Ra, 232 Th and 40 K from soils to corn and wheat plants have been studied by radiotracer experiments. Conclusion: The natural radioactivity levels in Eilam province are not at the range of high risk of morbidity and are under international standards. PMID:26056646

  13. 226Ra bioavailability to plants at the Urgeiriça uranium mill tailings site.

    PubMed

    Madruga, M J; Brogueira, A; Alberto, G; Cardoso, F

    2001-01-01

    Large amounts of solid wastes (tailings) resulting from the exploitation and treatment of uranium ore at the Urgeiriça mine (north of Portugal) have been accumulated in dams (tailing ponds). To reduce the dispersion of natural radionuclides into the environment, some dams were revegetated with eucalyptus (Eucalyptus globolus) and pines (Pinus pinea). Besides these plants, some shrubs (Cytisus spp.) are growing in some of the dams. The objective of this study is to determine the 226Ra bioavailability from uranium mill tailings by quantifying the total and available fraction of radium in the tailings and to estimate its transfer to plants growing on the tailing piles. Plant and tailing samples were randomly collected and the activity concentration of 226Ra in plants (aerial part and roots) and tailings was measured by gamma-spectrometry. The exchangeable fraction of radium in tailings was quantified using one single step extraction with 1 mol dm-3 ammonium acetate (pH = 7) or 1 mol dm-3 calcium chloride solutions. The results obtained for 226Ra uptake by plants show that 226Ra concentration ratios for eucalyptus and pines decrease at low 226Ra concentrations in the tailings and appear relatively constant at higher radium concentrations. For shrubs, the concentration ratios increase at higher 226Ra solid waste concentrations approaching a saturation value. Percentage values of 16.0 +/- 8.3 and 12.9 +/- 8.9, for the fraction of radium extracted from the tailings, using 1 mol dm-3 ammonium acetate or calcium chloride solutions, respectively, were obtained. The 226Ra concentration ratios determined on the basis of exchangeable radium are one order of magnitude higher than those based on total radium. It can be concluded that, at a 95% confidence level, more consistent 226Ra concentration ratios were obtained when calculated on the basis of available radium than when total radium was considered, for all the dams.

  14. Distribution and retention in bone of /sup 226/Ra and comparison with the ICRP 20 model

    SciTech Connect

    Holtzman, R.B.; Rundo, J.; Sha, J.Y.; Spaletto, M.I.

    1981-01-01

    Analyses are presented of the ratios of /sup 226/Ra to calcium in over 650 samples of compact and cancellous bone from 66 female and 26 male subjects who had died from less than one to 60 years after first exposure to radium. The /sup 226/Ra/Ca ratios were normalized to the terminal /sup 226/Ra skeletal content. The /sup 226/Ra/Ca ratios for vertebrae were essentialy identical to those for other cancellous bone for a given subject. Comparisons of the data with predictions of the ICRP model of alkaline earth metabolism show that for female cancellous bone the normalized /sup 226/Ra/Ca ratios tended to be greater than predicted, while those for female cortical bone (femoral and tibial shaft) tended to be less. The data for males were fitted better by the model. A modification of the model to reduce the amount of radium deposited in soft tissue fitted the data better in some respects. A straight line linear least squares fit to the data appeared to fit as well as, or better than, the models. A radiation effect was suggested in that the normalized /sup 226/Ra/Ca ratio for vertebrae relative to the ratio expected increased with skeletal absorbed dose for vertebra. However, no such effect was apparent for compact bone or for the cancellous bone as a whole.

  15. Transfer coefficient of 226Ra from vegetation to meadow voles, Microtus pennsylvanicus, on U mill tailings

    SciTech Connect

    Cloutier, N.R.; Clulow, F.V.; Lim, T.P.; Dave, N.K.

    1986-06-01

    The 226Ra level in vegetation growing on U mine tailings in Elliot Lake, Ontario, Canada, was 211 + 22 mBq g-1 (dry weight) compared to less than 7 mBq g-1 (dry weight) in material from a control site. Skeletons of meadow voles (Microtus pennsylvanicus) established on the tailings had concentrations of 226Ra of 6083 +/- 673 mBq per animal in winter; 7163 +/- 1077 mBq per animal in spring; 1506 +/- 625 mBq per animal in summer; and 703 +/- 59 mBq per animal in fall, compared to less than 7 mBq per animal in controls. The /sup 226/Ra transfer coefficient from vegetation to voles (defined as total millibecquerels of /sup 226/Ra in adult vole per total millibecquerels of 226Ra consumed by the vole in its lifetime) was calculated as 4.6 +/- 2.9 X 10(-2) in summer and 2.8 +/- 0.6 X 10(-2) in fall.

  16. Comparative Analysis Of 226Ra Soil-To-Plant Transfer In Cabbage Grown In Various Regions

    NASA Astrophysics Data System (ADS)

    Madruga, M. J.; Carvalho, F. P.; Silva, L.; Gouveia, J.

    2008-08-01

    The transfer of 226Ra from soil to cabbage was compared amongst regions, namely the surroundings of Urgeiriça uranium milling tailings (GE), regions with past uranium mining activities (GN1), and regions with no uranium mining activities and no uranium deposits (GN2). Results show a slight increase of the concentration ratio values at low radium concentration in soils. Statistical analysis of the mean 226Ra activity concentrations in soil and cabbage for the three regions was carried out. The comparison of 226Ra activity concentrations in soils indicated no difference (p>0.05), between GE and GN2 and significant differences (p<0.05) between GE and GN1 and between GN1 and GN2. Similar statistical results were obtained for 226Ra activity concentrations in cabbage from the same regions. It was concluded that radium Concentration Ratio (CR) for cabbage grown in the region of the main uranium milling site (GE) is of the same order of magnitude of CR in cabagge grown in background regions (GN2). However, 226Ra CR was higher in cabagge from the region with past uranium mining activities (GN1).

  17. Transfer coefficient of 226Ra from vegetation to meadow voles, Microtus pennsylvanicus, on U mill tailings.

    PubMed

    Cloutier, N R; Clulow, F V; Lim, T P; Davé, N K

    1986-06-01

    The 226Ra level in vegetation growing on U mine tailings in Elliot Lake, Ontario, Canada, was 211 + 22 mBq g-1 (dry weight) compared to less than 7 mBq g-1 (dry weight) in material from a control site. Skeletons of meadow voles (Microtus pennsylvanicus) established on the tailings had concentrations of 226Ra of 6,083 +/- 673 mBq per animal in winter; 7,163 +/- 1,077 mBq per animal in spring; 1,506 +/- 625 mBq per animal in summer; and 703 +/- 59 mBq per animal in fall, compared to less than 7 mBq per animal in controls. The 226Ra transfer coefficient from vegetation to voles (defined as total millibecquerels of 226Ra in adult vole per total millibecquerels of 226Ra consumed by the vole in its lifetime) was calculated as 4.6 +/- 2.9 X 10(-2) in summer and 2.8 +/- 0.6 X 10(-2) in fall.

  18. Release of 226Ra from uranium mill tailings by microbial Fe(III) reduction

    USGS Publications Warehouse

    Landa, E.R.; Phillips, E.J.P.; Lovley, D.R.

    1991-01-01

    Uranium mill tailings were anaerobically incubated in the presence of H2 with Alteromonas putrefaciens, a bacterium known to couple the oxidation of H2 and organic compounds to the reduction of Fe(III) oxides. There was a direct correlation between the extent of Fe(III) reduction and the accumulation of dissolved 226Ra. In sterile tailings in which Fe(III) was not reduced, there was negligible leaching of 226Ra. The behavior of Ba was similar to that of Ra in inoculated and sterile systems. These results demonstrate that under anaerobic conditions, microbial reduction of Fe(III) may result in the release of dissolved 226Ra from uranium mill tailings. ?? 1991.

  19. Concentrations of (226)Ra, (232)Th and (4)(0)K in industrial kaolinized granite.

    PubMed

    Todorović, Nataša; Hansman, Jan; Mrđa, Dušan; Nikolov, Jovana; Kardos, Richárd; Krmar, Miodrag

    2017-03-01

    Activity concentrations of (226)Ra, (232)Th and (4)(0)K in 120 kaolinized granite samples imported in Serbia from the Motajica mine, Bosnia and Herzegovina, were measured. The (226)Ra concentration ranged from 61 to 319 Bq kg(-1), the (232)Th from 44 to 272 Bq kg(-1), and the (4)(0)K from 590 to 1470 Bq kg(-1). The frequency distribution of (4)(0)K concentrations was near-Gaussian, where those of (226)Ra and (232)Th were right-skewed. In 6 samples, the gamma index, I, was higher than 2, which exceeds the exemption dose criterion (0.3 mSv y(-1)). The absorbed dose rate and annual effective doses for workers in the ceramic industries in Serbia who worked with kaolinized granite were below levels of concern.

  20. Removal of 226Ra and 228Ra from TENORM sludge waste using surfactants solutions.

    PubMed

    Attallah, M F; Hamed, Mostafa M; El Afifi, E M; Aly, H F

    2015-01-01

    The feasibility of using surfactants as extracting agent for the removal of radium species from TENORM sludge produced from petroleum industry is evaluated. In this investigation cationic and nonionic surfactants were used as extracting agents for the removal of radium radionuclides from the sludge waste. Two surfactants namely cetyltrimethylammonium bromide (CTAB) and Triton X-100 (TX100) were investigated as the extracting agents. Different parameters affecting the removal of both (226)Ra and (228)Ra by the two surfactants as well as their admixture were studied by the batch technique. These parameters include effect of shaking time, surfactants concentration and temperature as well as the effect of surfactants admixture. It was found that, higher solution temperature improves the removal efficiency of radium species. Combined extraction of nonionic and cationic surfactants produces synergistic effect in removal both (226)Ra and (228)Ra, where the removals reached 84% and 80% for (226)Ra and (228)Ra, respectively, were obtained using surfactants admixture.

  1. A rapid and inexpensive method for 226Ra and 228Ra measurements of high TDS groundwaters.

    PubMed

    El-Shrakawy, A; Ebaid, Y Y; Burnett, W C; Aldaihan, Soaad K

    2013-07-01

    A series of laboratory-scale studies was conducted by preconcentrating (226)Ra from spiked water test samples using Purolite ion-exchange resin to evaluate the adsorption efficiency of the resin under varying conditions. After removing the resin from the columns, it was sealed in gas-tight containers and measured via gamma spectrometry. The Purolite resin showed high radium uptake and retention from natural waters in the presence of high iron and total dissolved solids (TDS). This procedure allowed us to process a large number of high TDS samples at a typical rate of 15 samples/day using three germanium detectors. Quality assurance and method validation have been achieved by analyzing selected groundwater samples, with different (226)Ra activities and high TDS values, and comparing the results to those using alpha spectrometry with a (133)Ba yield tracer. There was very good agreement between the obtained (226)Ra activities by both methods.

  2. Bioaccumulation of 226Ra by plants growing in fresh water ecosystem around the uranium industry at Jaduguda, India.

    PubMed

    Jha, V N; Tripathi, R M; Sethy, N K; Sahoo, S K; Shukla, A K; Puranik, V D

    2010-09-01

    A field study has been conducted to evaluate the (226)Ra bioaccumulation among aquatic plants growing in the stream/river adjoining the uranium mining and ore-processing complex at Jaduguda, India. Two types of plant group have been investigated namely free floating algal species submerged into water and plants rooted in stream & riverbed. The highest (226)Ra activity concentration (9850 Bq kg(-1)) was found in filamentous algae growing in the residual water of tailings pond. The concentration ratios of (226)Ra in filamentous algae (activity concentration of (226)Ra in plant Bq kg(-1) fresh weight/activity concentration of (226)Ra in water Bq l(-1)) widely varied i.e. from 1.1 x 10(3) to 8.6 x 10(4). Other aquatic plants were also showing wide variability in the (226)Ra activity concentration. The ln-transformed filamentous algae (226)Ra activity concentration was significantly correlated with that of ln-transformed water concentration (r = 0.89, p < 0.001). There was no correlation between the activity concentrations of (226)Ra in stream/riverbed rooted plants and the substrate. For this group, correlation between (226)Ra activity concentration and Mn, Fe, Cu concentration in plants were statistically significant.

  3. Water hardness determines (226)Ra uptake in the tropical freshwater mussel.

    PubMed

    Doering, Che; Bollhöfer, Andreas

    2017-03-22

    Chemical data for freshwater mussels (Velesunio spp.) and water from 15 sampling sites in the Alligator Rivers Region and Rum Jungle uranium provinces in tropical Northern Australia were analysed to develop a predictive model of radium-226 ((226)Ra) bioaccumulation for variable water calcium (Ca) and magnesium (Mg) concentrations. Application of the model as a (226)Ra screening approach for freshwater mussels in tropical waterbodies potentially impacted by operational or remediated uranium mine sites is discussed in relation to Mudginberri Billabong, located approximately 12 km downstream of Ranger uranium mine in the Alligator Rivers Region.

  4. 226Ra activity in the mullet species Liza aurata and South Adriatic Sea marine.

    PubMed

    Antovic, N M; Antovic, I; Svrkota, N

    2010-08-01

    (226)Ra activity in the South Adriatic Sea-water, surface sediment, mud with detritus, seagrass (Posidonia oceanica) samples and the mullet (Mugilidae) species Liza aurata, as well as soil and sand from the Montenegrin Coast-was measured using the six-crystal gamma-coincidence spectrometer PRIPYAT-2M. The results are used for calculation of the absorbed (and annual effective) dose rates in air due to the (226)Ra gamma radiation. The absorbed dose rates ranged from 5.94 to 97.16 nGy h(-1) (soil) and from 0.65 to 7.65 nGy h(-1) (sand). In seawater (226)Ra activity is found to be from 0.08 to 0.15 Bq l(-1), while in whole L. aurata individuals from 0.58 to 1.97 Bq kg(-1). Annual intake of (226)Ra by human consumers of this fish species has been estimated to provide an effective dose of 0.006 mSv y(-1).

  5. Estuarine geochemistry of /sup 224/Ra, /sup 226/Ra, and /sup 222/Rn

    SciTech Connect

    Elsinger, R.J.

    1982-01-01

    Desorption from river borne sediments is the most likely source of the excess /sup 226/Ra. Laboratory mixing experiments on Pee Dee River sediments show an increase in /sup 226/Ra desorption with increasing salinities with maximum desorption occurring at or above 20/sup 0//oo salinity. Desorption and diffusion are the sources for /sup 226/Ra in the estuarine systems. In Winyah Bay the /sup 228/Ra//sup 226/Ra activity ratio does not change significantly with salinity, averaging around 1.4, indicating desorption as the major source of /sup 228/Ra. In the Yangtze River the /sup 228/Ra//sup 226/Ra activity ratio is constant (approx.1.90) until increasing linearly above 16/sup 0//oo. A diffusive flux from regeneration by /sup 232/Th decay in shelf sediments is the source of the increase. In Delaware Bay /sup 228/Ra increases faster than /sup 226/Ra in the less than or equal to22/sup 0//oo water, indicating a source in addition to desorption. The increase can be balanced by a 0.33 dpm/cm/sup 2/-year flux over the upper part of the Bay where fine grained sediments predominate. /sup 224/Ra behavior is controlled by its 3.64 day half-life. In Winyah Bay a flux of around 0.4 dpm/cm/sup 2/-day is necessary to support the standing crop of non-desorbed /sup 224/Ra in the water column. In Delaware Bay the nearly constant /sup 224/Ra in concentration over the 2.5/sup 0//oo to 12/sup 0//oo salinity range are maintained by regeneration from /sup 228/Th in the turbidity maximum zones and diffusion from bottom sediments. Water leaving on ebb tide from a salt marsh on Delaware Bay had increases in all three radium isotopes (/sup 224/Ra > /sup 228/Ra > /sup 226/Ra) compared to water coming in on the flood tide. Excess /sup 222/Rn concentrations in a fresh water section of the Pee Dee River show a decreasing downstream gradient. Using these gradients to determine evasion rates, stagnant film thicknesses range from 21..mu.. to 62..mu...

  6. A beta-alpha coincidence counting system for measurement of trace quantities of 238U and 232Th in aqueous samples at the Sudbury Neutrino Observatory.

    NASA Astrophysics Data System (ADS)

    Dawson, M.; Doucas, G.; Fergani, H.; Jelley, N. A.; Majerus, S.; O'Keeffe, H. M.; Peeters, S. J. M.; Perry, C.

    2016-08-01

    The Sudbury Neutrino Observatory experiment was built to measure the total flux of 8B solar neutrinos via the neutral current disintegration deuterium nuclei. This process can be mimiced by daughter isotopes of 232Th and 238U which can photodisintegrate the deuterium nucleus. Measurement of the concentration of such radioisotopes in the heavy water was critical to the success of the experiment. A radium assay technique using Hydrous Titanium Oxide coated filters was developed for this purpose and it was used in conjunction with a delayed beta-alpha coincidence counting system. The design, calibration and operation of this counting system are described in this paper. The counting efficiency for 232Th (224Ra) and 238U (226Ra) were measured to be 50 ± 5% and 62 ± 7%

  7. Study of contents of 226Ra, 232Th and 40K in fertilisers.

    PubMed

    Tahir, S N A; Alaamer, A S; Omer, R M

    2009-02-01

    In this study concentrations of naturally occurring radionuclides (226)Ra, (232)Th and (40)K were measured in the fertiliser samples in Pakistan using a high-resolution and high-purity germanium detector. Samples were collected from main fertiliser depots located in 10 big cities in the Punjab province. Gamma spectrometric analysis revealed that concentrations of (226)Ra, (232)Th and (40)K existed in the ranges from 232 to 511 Bq kg(-1), 21 to 58 Bq kg(-1) and 556 to 1302 Bq kg(-1) with average values of 386 +/- 92, 38 +/- 14 and 885 +/- 220 Bq kg(-1), respectively. Average values of the three natural radionuclides measured in this study were within the range of reported values from some of the other countries of the world. Correlations drawn between measured concentrations were not significant.

  8. Concentration of 210Po, 226Ra and 228Ac in non-siliceous environmental materials

    NASA Astrophysics Data System (ADS)

    Houmani, Zidan Mohamed M.; Bradley, D. A.; Maah, Mohd. Jamil; Ahmed, Zaharuddin

    2001-06-01

    The present interest concerns the possible anthropomorphic enhancement of naturally occurring radioactive material (NORM) in non-siliceous media, in particular, sediment from a river running alongside a crude oil facility and alluvial samples from the site of a now defunct minerals benefication plant. We use gamma spectrometry for 226Ra and 228Ac, and for 210Po we use alpha spectrometry in association with a hydrochloric acid based radiochemical method for the extraction of 210Po. Using 209Po to monitor polonium extraction from samples we find the concentrations of 210Po, 226Ra and 228Ac in river sediments to be in accord with typical background values (˜0.04 Bq g -1 dry), while for sub-surface soils located nearby we find the respective activity concentrations to accord with low background values (˜0.02 Bq g -1dry). For alluvial material from the site of a defunct minerals benefications plant we have found 210Po concentrations of ˜11 Bq g -1 (dry) in two of three samples and 30 Bq g -1 (dry) in the remaining sample; 226Ra and 228Ac were some several times these concentrations. In support of the methods we have adopted in present evaluations we find IAEA-300 Baltic Sea sediment reference material to contain 210Po concentrations that are within the IAEA confidence interval for this material.

  9. Effective dose to the public from 226Ra in drinking water supplies of Iran.

    PubMed

    Sohrabi, M; Beitollahi, M M; Hafezi, S; Asefi, M; Bolourchi, M

    1999-08-01

    One of the most important and prevalent isotopes of radium (Ra) in the human food chain, and especially in drinking water, is 226Ra. To determine the contribution of this radionuclide to the annual effective dose to the public in Iran, a national program for determination of this radionuclide was established. Over 500 water samples from different surface and ground water supplies including wells, rivers and springs, as well as hot springs and sea water from the Caspian Sea and Persian Gulf have been analyzed. An emanation method with a minimum detection limit of less than 2 mBq L(-1) was developed and applied in this study. Unweighted mean concentrations of 3.3 mBq L(-1) and 8.0 mBq L(-1) were determined in surface and ground drinking water supplies, respectively. Based on such values, mean unweighted annual intakes of 226Ra were found to be 0.85 Bq for an infant, 1.97 Bq for a child, and 2.82 Bq for an adult, which correspond to mean unweighted annual effective doses of 0.17 microSv y(-1), 0.39 microSv y(-1), and 0.56 microSv y(-1), respectively. The mean 226Ra concentrations in hot springs were higher with a maximum of 146.5 Bq L(-1) measured in the Ab-e-Siah hot spring in Ramsar, a town on the coast of the Caspian Sea in Iran.

  10. Concentration of 226Ra in rocks of the southern part of Lower Silesia (SW Poland).

    PubMed

    Przylibski, Tadeusz Andrzej

    2004-01-01

    The aim of the article is to present a preliminary description of rocks in the southern part of Lower Silesia and the Sudety Mountains in particular, with regard to 226Ra content. The research demonstrates that the average content of this isotope was 40.4 Bq/kg in the rocks of the southern part of Lower Silesia, and 41.7 Bq/kg in the rocks of the Sudetes. These values are slightly higher than the mean 226Ra content in the upper part of the Earth's crust, while the measured maximum content of this isotope (244 Bq/kg) is more than twice as high as the upper range of the values most frequently recorded in the upper part of the Earth's crust. The minimum values were lower than the detection limit, which was about 1 Bq/kg. These results reflect the mosaic-like geological structure of Lower Silesia, and particularly the Sudety Mountains, the occurrence of SiO2-rich igneous rocks and the products of their metamorphism, as well as numerous manifestations of uranium mineralisation or even deposital concentrations of this element. The rocks with the highest 226Ra contents include (in decreasing order): aplites, granites, gneisses and leucogranites, granite-gneisses, granodiorites and rhyolites, and, finally, mudstones. The lowest values of 226Ra content, on the other hand, were measured in sandstones, marls and conglomerates, and extremely low-in marbles and quartzites. The results show that background values of 226Ra content in the rocks of the southern part of Lower Silesia fall within a range from several to about 100 Bq/kg, which is the same as the range most frequently recorded in the upper part of the Earth's crust. Distribution of these values has log-normal character. The research demonstrates that the southern part of Lower Silesia, and the Sudetes in particular, may be marked by an increased radon potential. Particularly liable areas are: the Karkonosze granite massif, especially in its border zones, the Ladek-Snieznik and the Izera massifs, especially in their

  11. Internal [sup 238]U-series systematics of pumice from the November 13, 1985, eruption of Nevado de Ruiz, Colombia

    SciTech Connect

    Schaefer, S.J.; Williams, S.N. ); Sturchio, N.C. ); Murrell, M.T. )

    1993-03-01

    High-precision mass spectrometer and alpha scintillation measurements of [sup 238]U-series nuclides were obtained for whole-rock pumice and constituent mineral and glass separates to help interpret the timing and nature of magmatic processes that led up to the 1985 eruption of Nevado de Ruiz volcano. Internal isochron diagrams for [sup 226]Ra/Ba vs. [sup 230]Th/Ba and [sup 230]Th/[sup 232]Th vs. [sup 238]U/[sup 232]Th show that data define linear arrays, indicating an average crystallization age of 6.1 [+-] 0.5 ka (Ra-Th isochron) and 7 [+-] 6 ka (Th-U isochron). Stratigraphic, petrographic geochemical, repose time, and eruption volume data for the Holocene eruptive sequence of Nevado del Ruiz indicate that significant changes occurred in the subvolcanic magma chamber between eruptions R9 ([approx]8.6 ka) and R8 ([approx]3.0 ka). This coincides with the average crystallization age derived from the U-series data and may represent the injection of a new batch (or batches) of mantle-derived magma into the subvolcanic magma chamber. 26 refs., 4 figs., 2 tabs.

  12. Minimum speed limit for ocean ridge magmatism from 210Pb-226Ra-230Th disequilibria.

    PubMed

    Rubin, K H; van der Zander, I; Smith, M C; Bergmanis, E C

    2005-09-22

    Although 70 per cent of global crustal magmatism occurs at mid-ocean ridges-where the heat budget controls crustal structure, hydrothermal activity and a vibrant biosphere-the tempo of magmatic inputs in these regions remains poorly understood. Such timescales can be assessed, however, with natural radioactive-decay-chain nuclides, because chemical disruption to secular equilibrium systems initiates parent-daughter disequilibria, which re-equilibrate by the shorter half-life in a pair. Here we use 210Pb-226Ra-230Th radioactive disequilibria and other geochemical attributes in oceanic basalts less than 20 years old to infer that melts of the Earth's mantle can be transported, accumulated and erupted in a few decades. This implies that magmatic conditions can fluctuate rapidly at ridge volcanoes. 210Pb deficits of up to 15 per cent relative to 226Ra occur in normal mid-ocean ridge basalts, with the largest deficits in the most magnesium-rich lavas. The 22-year half-life of 210Pb requires very recent fractionation of these two uranium-series nuclides. Relationships between 210Pb-deficits, (226Ra/230Th) activity ratios and compatible trace-element ratios preclude crustal-magma differentiation or daughter-isotope degassing as the main causes for the signal. A mantle-melting model can simulate observed disequilibria but preservation requires a subsequent mechanism to transport melt rapidly. The likelihood of magmatic disequilibria occurring before melt enters shallow crustal magma bodies also limits differentiation and heat replenishment timescales to decades at the localities studied.

  13. Microdistribution and local dosimetry of /sup 226/Ra in trabecular bone of the beagle

    SciTech Connect

    Polig, E.; Jee, W.S.; Dell, R.B.; Johnson, F.

    1988-11-01

    Sections of lumbar vertebral bodies of young adult beagle dogs have been analyzed autoradiographically to characterize and quantify the local distribution of 226Ra by means of a scanning microscope photometer. The animals received a single injection of 355 kBq/kg body weight and were serially sacrificed at 5 to 1381 days postinjection. Hotspot concentrations decreased from about 51 kBq/g bone at 5 days to 20 kBq/g at 1381 days postinjection. The diffuse concentration changed from 8.3 to 1.9 kBq/g. The mean 226Ra concentration in the trabecular areas scanned was initially higher and at the end of the observation period lower than the average calculated for the whole lumbar vertebral column. Density and area of, and fraction of bone activity in, hotspots virtually remained constant. With time hotspots tended to become translocated into bone volume. Mean dose rates to lining cells from both hotspots and diffuse labels decreased from about 210 mGy/d at early postinjection times to 105 mGy/d. This corresponds to 2.5 to 1.1 times the average skeletal dose rate. A discussion of the level of irradiation in terms of hit frequencies shows that osteoblasts in the initial phase of hotspot formation receive about 60 hits to their nucleus for the duration of bone formation. After about 6 months, however, the 226Ra concentration in new bone and the corresponding hit frequency appears to be low enough that interference with bone formation is unlikely. Morphometric measurements showed that abnormal bone accretion and thickening of trabeculae occurred. This was interpreted as an imbalance between bone formation and resorption. Both formation and resorption seem to be substantially lowered compared to control animals.

  14. Fixation of radionuclides in the 238U decay series in the vicinity of mineralized zones: 1. The Austatom Uranium Prospect, Northern Territory, Australia

    NASA Astrophysics Data System (ADS)

    Shirvington, P. J.

    1983-03-01

    The minimum age of a zone of secondary uranium mineralization, located at the Austatom Prospect in the Alligator Rivers region of Australia, is estimated to be 3.6 × 10 5y. This is derived from a geochronological model based on retarded leaching of 234U with respect to 238U and on ratios within the ore of these members of the 238U decay series. Although kaolinite is a dominant mineral in the weathered schist-host-rocks, retarded dissolution of 234U occurs only in the presence of the clay minerals illite and montmorillonite. In their absence the reverse occurs. A model is proposed to explain the results. Ratios of 230Th to 238U indicate that the mineralization has probably remained stationary within the weathered schist for at least 1 to 2 × 10 5y. Future use of clay minerals as buffers in radioactive waste repositories is supported by the excellent long-term retention obtained for oxidized uranium, probably due in part to isomorphic substitution into the clay crystal lattice.

  15. Natural radioactivity of 226Ra and 228Ra in thermal and mineral waters in Croatia.

    PubMed

    Bituh, Tomislav; Marovic, Gordana; Petrinec, Branko; Sencar, Jasminka; Franulovic, Iva

    2009-01-01

    Thermal waters are known as valuable natural resources of a country. They contain certain degree of natural radioactivity attributable to the elements of the uranium and thorium natural decay series. Among these elements, the most radiotoxic and the most important is radium that exists in several isotopic forms (226Ra and 228Ra). The focus of attention was the content of radium in samples of thermal and mineral spring water from several spas in Croatia. These waters are mainly used for medical, bathing and recreational purposes, and some of them are used for drinking. Measured activity concentrations of 226Ra ranged from 87 to 6200 mBq l(-1) which, in some springs, exceed the maximal permissible level of 1 Bq l(-1) for drinking water. Measured activity concentrations of 228Ra ranged from 23 to 3480 mBq l(-1). The study showed that radium content for the investigated thermal and mineral waters is below the levels at which negative consequences would arise due to ingestion.

  16. Techniques for precise mapping of 226Ra and 228Ra in the ocean

    NASA Astrophysics Data System (ADS)

    Moore, Willard S.; Key, Robert M.; Sarmiento, Jorge L.

    1985-01-01

    Improvements in the analyses of 226Ra and 228Ra in seawater made possible by better extraction and processing techniques reduce significantly the errors associated with these measurements. These improvements and the extensive sampling for Ra isotopes conducted on the TTO North Atlantic Study should enable us to use the distribution of 228Ra to study mixing processes on a 3-15 year time scale in both the upper and deep North Atlantic. The 228Ra profiles already analyzed show a closer resemblance to GEOSECS tritium data than to TTO tritium data in the upper ocean. This is because the transient tracer tritium was responding on a 10-year time scale during GEOSECS and a 20-year time scale during TTO. The steady state tracer 228Ra should always respond on a time scale of 8 years. Thus the 228Ra data obtained on TTO should provide a means to extend the features of the GEOSECS tritium field to the regions of the TTO study. The 226Ra data are of high enough quality to identify features associated with different water masses. Changes in the positions of the deep-water masses since the GEOSECS cruise are revealed by the 226Radata.

  17. Bone tumor location in dogs given skeletal irradiation by {sup 239}Pu or {sup 226}Ra

    SciTech Connect

    Lloyd, R.D.; Taylor, G.N.; Miller, S.C.

    1997-10-01

    Statistical analyses have indicated that there was a significant difference between dogs injected with bone volume-seeking {sup 226} Ra as compared to those given bone surface-seeking {sup 239}Pu with respect to location within the skeleton of 334 radiation-induced primary bone malignancies. Corresponding differences also were event when dogs given bone volume-seeking {sup 90}Sr or bone surface-seeking {sup 241}Am, {sup 228}Th {sup 248,252}Cf, or {sup 224}Ra (which decays mostly on bone surfaces because of its short, 3.6 d half time) were included along with the {sup 226}Ra or {sup 239}Pu, respectively (562 total tumors). Further analysis suggested that higher values of percent red marrow (M) and bone turnover rate (R) are correlated with increased probability. of tumor appearance at a particular location within the skeleton for the surface seekers. Proportionately higher values of M and R are associated with skeletal sites containing mostly trabecular bone as compared to those with mostly compact (cortical) bone. Coefficients of determination (r{sup 2}) for the relationship between percent of total tumors vs the combination of percent red marrow and turnover rate (= MR) was about 0.7 for the surface seekers but only about 0.1 for the volume seekers. This indicates that the neoplastic effects of surface seekers, but not volume seekers, are associated with the presence of trabecular bone at the various sites of radio nuclide deposition within the skeleton. 10 refs., 3 tabs.

  18. The estuarine chemistry and isotope systematics of 234,238U in the Amazon and Fly Rivers

    USGS Publications Warehouse

    Swarzenski, P.; Campbell, P.; Porcelli, D.; McKee, B.

    2004-01-01

    Natural concentrations of 238U and ??234U values were determined in estuarine surface waters and pore waters of the Amazon and Fly (Papua New Guinea) Rivers to investigate U transport phenomena across river-dominated land-sea margins. Discharge from large, tropical rivers is a major source of dissolved and solid materials transported to the oceans, and are important in defining not only oceanic mass budgets, but also terrestrial weathering rates. On the Amazon shelf, salinity-property plots of dissolved organic carbon, pH and total suspended matter revealed two vastly contrasting water masses that were energetically mixed. In this mixing zone, the distribution of uranium was highly non-conservative and exhibited extensive removal from the water column. Uranium removal was most pronounced within a salinity range of 0-16.6, and likely the result of scavenging and flocculation reactions with inorganic (i.e., Fe/Mn oxides) and organic colloids/particles. Removal of uranium may also be closely coupled to exchange and resuspension processes at the sediment/water interface. An inner-shelf pore water profile indicated the following diagenetic processes: extensive (???1 m) zones of Fe(III) - and, to a lesser degree, Mn(IV) - reduction in the absence of significant S(II) concentrations appeared to facilitate the formation of various authigenic minerals (e.g., siderite, rhodocrosite and uraninite). The pore water dissolved 238U profile co-varied closely with Mn(II). Isotopic variations as evidenced in ??234U pore waters values from this site revealed information on the origin and history of particulate uranium. Only after a depth of about 1 m did the ??234U value approach unity (secular equilibrium), denoting a residual lattice bound uranium complex that is likely an upper-drainage basin weathering product. This suggests that the enriched ??234U values represent a riverine surface complexation product that is actively involved in Mn-Fe diagenetic cycles and surface

  19. Plant/soil concentration ratios of 226Ra for contrasting sites around an active U mine-mill.

    PubMed

    Ibrahim, S A; Whicker, F W

    1988-12-01

    Concentrations of 226Ra were determined in native vegetation and underlying substrate (soil and tailings) at various sites around a conventional open-pit, acid leach U production operation in Wyoming. Plant/soil concentration ratios (CRs) for 226Ra were estimated for various sites, including weathered tailings; a tailings impoundment shoreline; downwind from exposed tailings; a mine overburden reclamation area; and several background locations. Radium-226 concentrations for vegetation and substrate and CR values from the perturbed sites were elevated above background. The highest vegetation concentration (1.3 Bq g-1) was found in a grass which had invaded exposed, weathered tailings. Levels of 226Ra in soil and vegetation and CR values decreased with distance from the tailings impoundment edge. CR values varied significantly among sites, but few differences were found between plant species groups. The observed CR values ranged from 0.07 at the background and reclamation areas to 0.4 downwind from the tailings area. Average CR values for plants growing on exposed tailings and within one meter from the impoundment edge were 0.15 and 0.3, respectively. CR values of 226Ra for plants on tailings substrates were comparatively low in contrast to other radionuclides in the U chain. We speculate that in the case of sulfuric acid leached tailings-derived material, 226Ra is sequestered as sulfate, which is highly insoluble relative to the sulfates of the other elements (e.g., U and Th) resulting in reduced availability for plant uptake.

  20. Disequilibrium between [sup 226]Ra and supported [sup 210]Pb in a sediment core from a shallow Florida lake

    SciTech Connect

    Brenner, M.; Peplov, A.J.; Schelske, C.L. )

    1994-07-01

    [sup 210]Pb dating can be used to assign ages in lake sediment cores, calculate rates of sediment accumulation, and determine the timing of recent changes in lake-watershed ecosystems. We used low-background gamma counting to measure [sup 226]Ra and total [sup 210]Pb activity in a core from Lake Rowell, Florida. [sup 226]Ra activity was high and strongly variable throughout the core, even exceeding total [sup 210]Pb activity in recently deposited sediments. We traced one source of Ra-rich sediments to the only inflow, Alligator Creek, where stream-bottom deposits display disequilibrium between [sup 226]Ra and supported [sup 210]Pb. High and variable [sup 226]Ra activity in the Lake Rowell profile argues for direct estimates of in situ Ra in lake sediment cores from disturbed watersheds that have Ra-bearing bedrock. Isotopic disequilibrium between [sup 226]Ra and supported [sup 210]Pb makes it difficult to distinguish between supported and unsupported [sup 210]Pb activity throughout the Lake Rowell core and would require special assumptions and nonconventional dating models to establish age-depth relationships. 78 refs., 3 figs., 1 tab.

  1. Comparative Analysis Of {sup 226}Ra Soil-To-Plant Transfer In Cabbage Grown In Various Regions

    SciTech Connect

    Madruga, M. J.; Carvalho, F. P.; Silva, L.; Gouveia, J.

    2008-08-07

    The transfer of {sup 226}Ra from soil to cabbage was compared amongst regions, namely the surroundings of Urgeirica uranium milling tailings (GE), regions with past uranium mining activities (GN1), and regions with no uranium mining activities and no uranium deposits (GN2). Results show a slight increase of the concentration ratio values at low radium concentration in soils. Statistical analysis of the mean {sup 226}Ra activity concentrations in soil and cabbage for the three regions was carried out. The comparison of {sup 226}Ra activity concentrations in soils indicated no difference (p>0.05), between GE and GN2 and significant differences (p<0.05) between GE and GN1 and between GN1 and GN2. Similar statistical results were obtained for {sup 226}Ra activity concentrations in cabbage from the same regions. It was concluded that radium Concentration Ratio (CR) for cabbage grown in the region of the main uranium milling site (GE) is of the same order of magnitude of CR in cabagge grown in background regions (GN2). However, {sup 226}Ra CR was higher in cabagge from the region with past uranium mining activities (GN1)

  2. Coulomb excitation of states in 238U

    NASA Astrophysics Data System (ADS)

    McGowan, F. K.; Milner, W. T.

    1994-05-01

    Twenty-two states in 238U have been observed with 18 MeV 4He ions on a thick target. Eight 2 + states between 966 and 1782 keV and three 3 - states are populated by direct E2 and E3, respectively. The remaining states are either weakly excited by multiple Coulomb excitation and /or populated by the γ-ray decay of the directly excited states. Spin assignments are based on γ-ray angular distributions. Reduced transition probabilities have been deduced from the γ-ray yields. The B(E2) values for excitation of the 2 + states range from 0.10 to 3.0 W.u. (281 W.u. for the first 2 + state). For the 3 states, the B(E3, 0 → 3 -) values are 7.1, 7.8, and 24.2 W.u. Several of the 2 + states have decay branches to the one-phonon states with B(E2) values between 27 and 56 W.u. which are an order of magnitude larger than the B(E2) values between the one- and zero-phonon states. This disagrees with our present understanding of collectivity in nuclei if these 2 + states are considered to be collective two-phonon excitations. However, the excitation energies of these 2 + states with respect to the one-phonon states are only 1.3 to 1.6. The B(E1) values for 17 transitions between the positive- and negative-parity states range between 10 -3 and 10 -7 W.u. The B(E1) branching ratios for many of these transitions have large deviations from the Alaga-rule predictions. These deviations can be understood by the strong Coriolis coupling between the states of the one-phonon octupole quadruplet in deformed nuclei. The general features of the experimental results for the B(E3) values are reproduced by the microscopic calculations of Neergård and Vogel when the Coriolis coupling between the states of the octupole quadruplet is included.

  3. 226Ra measurement in Mo, Cd and Nd 2O 3 samples with the emanation method

    NASA Astrophysics Data System (ADS)

    Barabash, A. S.; Barabanov, I. R.; Kornoukhov, V. N.; Orekhov, I. V.

    2001-08-01

    Measurements of 226Ra content in materials and chemical reagents used to construct the double beta decay sources in the NEMO-3 experiment have been done with the emanation method technique. Three different radon emanation technologies were used in these studies. The first was the "traditional" method of dissolving the sample. The second was an extraction of Rn from a melted sample and finally a technique of heating fine-grained powder was used. It is shown that there is good agreement of the data received with the emanation method and low background high purity germanium detectors. The sensitivity of this method is 0.02 mBq/ l of solution (for the "standard" emanation method) or 0.02 mBq/ kg (for methods in which radon is extracted from a powder or melt).

  4. Use of 210Pb/ 226Ra disequilibria in the dating of deep-sea whale falls

    NASA Astrophysics Data System (ADS)

    Schuller, Daniel; Kadko, David; Smith, Craig R.

    2004-02-01

    Deep-sea whale falls, in particular the skeletal remains of whales that have sunk to the seafloor, are remarkable temporary reducing habitats. Reduced chemical species created by anaerobic microbial decay of lipid and organic compounds within the whale bone matrix fuel chemosynthetic-based communities, including bacteria, mussels, limpets, snails, and clams. Many of these species exhibit taxonomic affinities to other chemosynthetic deep-sea organisms colonizing hydrothermal vents and cold seeps. Knowledge of the timescales of whale fall community succession and persistence of these assemblages is needed to reliably estimate the abundance of whale fall habitats and to understand the dynamics of the whale fall communities and their potential roles as stepping stones for sulfophilic species. We have developed a radiochemical method based on 210Pb/ 226Ra disequilibria for estimating the ages of seafloor whale bone communities. Measurements of 210Pb/ 226Ra performed on known age bone samples yielded radioisotope ages in good agreement with the known ages. Our results indicate that this technique is valid for bones 10-85 years old (time since cetacean death). This technique, applied to multiple bones of unknown age whale falls taken from Monterey Canyon, Santa Catalina Basin, and San Nicholas Basin, constrained the upper limit ages of these systems (in 2002) to 6.3±1.0 years, 44.0±7.0 to 53.4±8.3 years, and 66.4±9.6 to 82.6±11 years, respectively. These ages were in reasonable agreement with faunal and/or skeletal observations. In addition, a preliminary lipid degradation rate was calculated for the Santa Catalina Basin whale fall using an independent time series and calibrated to the radiochemically determined age. Both radiochemical and lipid degradation evidence suggest that the whale fall microhabitat is able to support life for many decades.

  5. Sources of alluvium in a coastal plain stream based on radionuclide signatures from the 238U and 232Th decay series

    NASA Astrophysics Data System (ADS)

    Yeager, Kevin M.; Santschi, Peter H.; Phillips, Jonathan D.; Herbert, Bruce E.

    2002-11-01

    Discerning alluvial sources and their change over time or distance is a fundamental question in hydrology and geology, often critical in identifying impacts of human and natural perturbations on fluvial systems. Surfaces of upland interfluves and subsoils, sources of alluvium in the lower Loco Bayou basin, Texas, were distinguished using the isotope ratios 226Ra/232Th, 226Ra/230Th, and 230Th/232Th. Channel alluvium indicates a transition from interfluve surface to subsoil sources during flood (subsoil ˜34% to ˜91%, over about 8 km) and bank-full stages (subsoil ˜9% to ˜74%, over about 12 km), with distance downstream. These results indicate strong coupling between hillslope and channel processes, reflecting land use change from forested to agricultural, concentrated in lower Loco Bayou. This methodology shows that sediment sources can be differentiated based upon landscape placement where lithologic contrast is absent. The geochemistry, long half-lives, and fractionation of 238U and 232Th decay series radionuclides during pedogenic and fluvial processes in humid climates suggest that these methods are applicable in a wide variety of fluvial systems.

  6. Reply to Comment on “Steady-state 226Ra/230Th disequilibrium in mantle minerals: implications for melt transport rates in island arcs” by R. George, M. Reagan, S. Turner, J. Gill, B. Bourdon

    NASA Astrophysics Data System (ADS)

    Feineman, M. D.; DePaolo, D. J.

    2004-12-01

    We agree with George et al. that high 226Ra/ 230Th and correlated Ba/Th, 238U/ 230Th, and other elemental and isotopic ratios are the result of fluid addition to the wedge. The Feineman and DePaolo [Earth Planet. Sci. Lett. 215 (2003) 339-355] manuscript addresses more specifically the pathway followed by the fluid en route to the surface. In particular, we address whether the 226Ra/ 230Th data directly yield the total time available for the fluid to migrate from the point of origin in the slab to the melting region in the wedge, and ultimately to the surface with the melt. All of the processes involved in generating arc volcanism would of necessity have to take place very rapidly within the constraints proposed by George et al. The alternative is that the upward fluid movement is hindered by the fluid flow regime and solid mantle flow, allowing more time for reaction with the mantle wedge. There is evidence in the U-series data for more than one time scale, and our model helps to explain how this could come about. The extent to which grainscale 226Ra/ 230Th disequilibrium affects the inferred melt transport time is yet another issue, and this could be achieved either with the small-degree melt mechanism we discussed or by additional effects associated with melt and fluid migration at later stages in the melt generation process. We agree that the final melt transport event is likely to happen quickly. One of the most puzzling features of volcanic arcs is that the volcanic front emerges considerably behind the presumed location of primary water release from the subducting slab (depth to slab is ˜120 km beneath the volcanic front, as opposed to the predicted ˜80 km). This offset between the expected site of fluid release and the location of the volcanic front can be attributed to coupled transport of the fluid—in the form of hydrous minerals, such as amphibole and/or phlogopite in the wedge [J. Geophys. Res. 97 (1992) 2037-2070] or redirection of the melt due to

  7. Measurement of 224Ra and 226Ra activities in natural waters using a radon-in-air monitor

    USGS Publications Warehouse

    Kim, G.; Burnett, W.C.; Dulaiova, H.; Swarzenski, P.W.; Moore, W.S.

    2001-01-01

    We report a simple new technique for measuring low-level radium isotopes (224Ra and 226Ra) in natural waters. The radium present in natural waters is first preconcentrated onto MnO2-coated acrylic fiber (Mn fiber) in a column mode. The radon produced from the adsorbed radium is then circulated through a closed air-loop connected to a commercial radon-in-air monitor. The monitor counts alpha decays of radon daughters (polonium isotopes) which are electrostatically collected onto a silicon semiconductor detector. Count data are collected in energy-specific windows, which eliminate interference and maintain very low backgrounds. Radium-224 is measured immediately after sampling via 220Rn (216Po), and 226Ra is measured via 222Rn (218Po) after a few days of ingrowth of 222Rn. This technique is rapid, simple, and accurate for measurements of low-level 224Ra and 226Ra activities without requiring any wet chemistry. Rapid measurements of short-lived 222Rn and 224Ra, along with long-lived 226Ra, may thus be made in natural waters using a single portable system for environmental monitoring of radioactivity as well as tracing of various geochemical and geophysical processes. The technique could be especially useful for the on-site rapid determination of 224Ra which has recently been found to occur at elevated activities in some groundwater wells.

  8. Validation of a procedure for the analysis of (226)Ra in naturally occurring radioactive materials using a liquid scintillation counter.

    PubMed

    Kim, Hyuncheol; Jung, Yoonhee; Ji, Young-Yong; Lim, Jong-Myung; Chung, Kun Ho; Kang, Mun Ja

    2017-01-01

    An analytical procedure for detecting (226)Ra in naturally occurring radioactive materials (NORMs) using a liquid scintillation counter (LSC) was developed and validated with reference materials (zircon matrix, bauxite matrix, coal fly ash, and phosphogypsum) that represent typical NORMs. The (226)Ra was released from samples by a fusion method and was separated using sulfate-coprecipitation. Next, a (222)Rn-emanation technique was applied for the determination of (226)Ra. The counting efficiency was 238 ± 8% with glass vials. The recovery for the reference materials was 80 ± 11%. The linearity of the method was tested with different masses of zircon matrix reference materials. Using 15 types of real NORMs, including raw materials and by-products, this LSC method was compared with γ-spectrometry, which had already been validated for (226)Ra analysis. The correlation coefficient for the results from the LSC method and γ-spectrometry was 0.993 ± 0.058.

  9. Distribution of (226)Ra-(210)Pb-(210)Po in marine biota and surface sediments of the Red Sea, Sudan.

    PubMed

    Sirelkhatim, D A; Sam, A K; Hassona, R K

    2008-12-01

    Activity concentration levels and ratios of (226)Ra, (210)Pb and (210)Po are presented in multicellular marine algae, molluscs, coral as well as in surface marine sediments collected from the shallower waters of the fringing reefs area extending towards north and south (Flamingo bay) of PortSudan harbour, Sudan. The analyses were performed adopting alpha-spectrometry, liquid scintillation and Cerenkov counting techniques. Surface sediments from this coastal region are poor in their radioactivity content in contrast to similar data reported from different coastal areas around the globe. There is surface enrichment of (210)Pb and (210)Po with respect to their progenitor (226)Ra as it is evident from the activity ratios of (210)Pb/(226)Ra (3.03+/-1.79) and (210)Po/(226)Ra (2.23+/-1.56). Among marine plants and animals investigated, the green algae species, Halimeda, and coral species, Favites, show substantial concentration of radium at 8.2Bq/kg and 21.9Bq/kg dry weight, respectively. Similarly, the highest concentration of (210)Po was met in Favites at 38.7Bq/kg followed by brown algae, Cystoseria sp., at 32.6Bq/kg. There is no variation seen among algal species for (210)Pb uptake, however, converse to radium and polonium, Favites (coral) was found to contain the minimum concentration of lead (3.88Bq/kg). In most species there is preferential accumulation of polonium over its parent radium as indicated by (210)Po:(226)Ra activity ratio with Cystoseria (brown algae) showing the highest value at 8.81. On the other hand, (210)Po:(210)Pb activity concentration ratio revealed that coral species Favites (9.97) and the brown algae Sargassum (1.85) have a greater tendency to accumulate (210)Po over (210)Pb, while in the rest of species; this ratio is less than unity.

  10. Low impact of exposure to environmentally relevant doses of 226Ra in Atlantic cod (Gadus morhua) embryonic cells.

    PubMed

    Olsvik, Pål A; Berntssen, Marc H G; Hylland, Ketil; Eriksen, Dag Ø; Holen, Elisabeth

    2012-07-01

    The aim of this study was to investigate whether (226)Ra, a radionuclide present in produced water from oil platforms in the North Sea and other offshore drilling areas, could affect vulnerable early life stages of Atlantic cod (Gadus morhua). Blastula-stage embryonic cells (EC) from fertilized eggs of Atlantic cod were isolated and exposed to environmental relevant concentrations of (226)Ra and transcription of selected genes quantified. The results showed a weak, but significant up-regulation of GPx3 and HSP70 transcripts after 48 h of exposure to 2.11 Bq/L. In EC exposed to three (226)Ra concentrations (2.11, 23 and 117 Bq/L) for 12 h, metallothionein, HSP90AA, thioredoxin and caspase 8 were significantly up-regulated in cells exposed to 117 Bq/L, whereas thioredoxin was also significantly up-regulated in EC exposed to 23 Bq/L. When EC were exposed to the same (226)Ra concentrations for 48 h, only heme oxygenase was significantly up-regulated in the 23 Bq/L exposure group. The results suggest that environmentally relevant activities of (226)Ra may induce oxidative stress and apoptosis in fish ECs. Exposure of Atlantic cod EC to Cd, selected as a model toxicant, supported the ability of EC around blastula stage to respond to toxicants by altered transcription. Due to dilution, environmentally relevant concentrations of radionuclides present in produced water would be expected to pose a minor threat to early life stages of fish.

  11. 238U series isotopes and 232Th in carbonates and black shales from the Lesser Himalaya: implications to dissolved uranium abundances in Ganga-Indus source waters.

    PubMed

    Singh, S K; Dalai, Tarun K; Krishnaswami, S

    2003-01-01

    238U and (232)Th concentrations and the extent of (238)U-(234)U-(230)Th radioactive equilibrium have been measured in a suite of Precambrian carbonates and black shales from the Lesser Himalaya. These measurements were made to determine their abundances in these deposits, their contributions to dissolved uranium budget of the headwaters of the Ganga and the Indus in the Himalaya and to assess the impact of weathering on (238)U-(234)U-(230)Th radioactive equilibrium in them. (238)U concentrations in Precambrian carbonates range from 0.06 to 2.07 microg g(-1). The 'mean' U/Ca in these carbonates is 2.9 ng U mg(-1) Ca. This ratio, coupled with the assumption that all Ca in the Ganga-Indus headwaters is of carbonate origin and that U and Ca behave conservatively in rivers after their release from carbonates, provides an upper limit on the U contribution from these carbonates, to be a few percent of dissolved uranium in rivers. There are, however, a few streams with low uranium concentrations, for which the carbonate contribution could be much higher. These results suggest that Precambrian carbonates make only minor contributions to the uranium budget of the Ganga-Indus headwaters in the Himalaya on a basin wide scale, however, they could be important for particular streams. Similar estimates of silicate contribution to uranium budget of these rivers using U/Na in silicates and Na* (Na corrected for cyclic and halite contributions) in river waters show that silicates can contribute significantly (approximately 40% on average) to their U balance. If, however, much of the uranium in these silicates is associated with weathering resistant minerals, then the estimated silicate uranium component would be upper limits. Uranium concentration in black shales averages about 37 microg g(-1). Based on this concentration, supply of U from at least approximately 50 mg of black shales per liter of river water is needed to balance the average river water U concentration, 1.7 microg L

  12. Gamma-ray spectroscopy of the ^238U shape isomer.

    NASA Astrophysics Data System (ADS)

    Hauschild, K.; Bauer, R. W.; Becker, J. A.; Bernstein, L. A.; Britt, H. C.; Younes, W.; Fotiades, N.

    1997-04-01

    The γ--rays de--exciting the fission isomers ^236U and ^238U are very different despite similar excitation energies, lifetimes and low--lying yrast structures. The predominant γ--ray decay branch for ^236U^m is a 1.783 MeV E1 transition (J. Schirmer, et al., Phys. Rev. Lett. 63), 2196 (1989); and Refs. therein., while ^238U^m is depopulated by a 2.513 MeV E2 γ-ray (J. Kantele, et al., Phys. Rev. C 29), 1693 (1984); and Refs. therein.. Approximately 65% of the γ--branch de-exciting ^238U^m remains to be identified. To determine the multipolarity of the remaining γ-branch out of ^238U^m we used the Gammasphere array at LBNL and the ^238U(d,pn) reaction at Ed = 20 MeV. A search for excited states in the 2^nd well has also been conducted. Preliminary results will be presented, and the γ--decay of the shape isomers discussed in context with the recent A ~190 SD decay--out results (T. L. Khoo, et al., Phys. Rev. Lett. 76), 1583 (1996); A. Lopez-Martens, et al., Phys. Lett. B380, 18 (1996); K. Hauschild, et al., submitted to Phys. Rev. C (1996)..

  13. Leaching of 226Ra from U mill tailings by sulfate-reducing bacteria.

    PubMed

    Landa, E R; Miller, C L; Updegraff, D M

    1986-10-01

    Relatively insoluble sulfate precipitates appear to be a major host for Ra in sulfuric acid-treated, U mill tailings. The dissolution of such precipitates by natural processes, such as metabolism by sulfate-reducing bacteria (SRB), creates the potential for release of Ra to contacting waters. Significant leaching of Ra by SRB was achieved in the laboratory during the anaerobic incubation (1 to 119 days) of U mill tailings with pure cultures of Desulfovibrio desulfuricans and mixed cultures containing SRB isolated from the tailings, all grown on a lactate medium at room temperature. While the maximum 226Ra concentration reached in a sterile media control was 0.44 Bq/L (12 pCi/L), that in the SRB systems was 61 Bq/L (1640 pCi/L) or about 20% of the total Ra inventory in the original tailings sample. The leaching of Ra in SRB systems was accompanied by a decrease in soluble sulfate concentration, an increase in total sulfide concentration, and an increase in the number of SRB. The observed leaching effect does not appear to be due to the action of microbial chelates or to binding to cell walls. Potential implications of these findings to the management of U mill tailings and other radioactive wastes are discussed.

  14. Thermoluminescence and excess 226Ra decay dating of late Quaternary fluvial sands, East Alligator River, Australia

    NASA Astrophysics Data System (ADS)

    Murray, Andrew; Wohl, Ellen; East, Jon

    1992-01-01

    Thermoluminescence (TL) dating was applied to seven samples of siliceous fluvial sands from the East Alligator River of Northern Australia, giving ages ranging from modern to 6000 yr B.P. Two methods of estimating the equivalent dose (ED), total bleach and regenerative, were applied to the 90- to 125-μm quartz fraction of the samples in order to determine the reliability and internal consistency of the technique. High-resolution γ and α spectroscopy were used to measure radionuclide contents; these measurements revealed an excess 226Ra activity compared with 230Th. This excess decreased with depth, and was used directly to derive mean sedimentation rates, and thus sediment ages. Both this method and one 14C date confirmed the validity of the TL values, which increased systematically with depth and were consistent with site stratigraphy. TL was of limited use in the dating of these late Holocene deposits because of age uncertainties of 500 to 1600 yr, resulting from a significant residual ED. This residual probably resulted from incomplete bleaching during reworking upstream of the sampling site. For Pleistocene deposits, the residual ED will be less significant because of higher total EDs, and TL dates will be correspondingly more accurate.

  15. Soft-tissue tumors among beagles injected with {sup 226}Ra

    SciTech Connect

    Lloyd, R.D.; Taylor, G.N.; Angus, W.

    1994-03-01

    A total of 409 primary soft-tissue tumors (189 malignant) occurred among 87 of 120 young adult beagles (72.5%) injected with {sup 226}Ra in eight dose levels ranging from 0.2-440 kBq kg{sup -1} body mass, while a total of 565 primary soft-tissue tumors (208 of them malignant) were seen among 117 of 133 control beagles not given radioactivity (88%). Because the p-value for the difference in these two percentages was >0.05, further comparisons were not made of all tumor locations or types taken together but only of the individual tumor locations or types. There was a clear excess of malignant tumors and all tumors (benign plus malignant) in the eye among dogs injected with radium (p < 0.05, p < 0.01, respectively), but the occurrence of all the other types of soft-tissue tumors was not greater in irradiated vs. control dogs (p > 0.05). This was also true for hematopoietic tumor types (including just one leukemia in a control and none in irradiated dogs) in which there was no difference between controls and dogs given radium. 25 refs., 7 tabs.

  16. The Concentrations of {sup 40}K, {sup 226}Ra and {sup 232}Th in Soil Sample in Osmaniye (Turkey)

    SciTech Connect

    Akkurt, I.; Guenoglu, K.; Kara, A.; Mavi, B.; Karaboerklue, S.

    2011-12-26

    The {sup 40}K, {sup 226}Ra and {sup 232}Th concentration is due to the magmatic structure of the earth and it can be varied from place to place. Osmaniye is located in the Eastern side of Mediteranean Region. It holds the climatic characteristics of the same region and arises with Middle Taurus Mountains from west to North and with Amonos Mounations in East and West-east parts and is situated between 35 deg. .52'-36 deg. .42' east longitudes and 36 deg. .57'-37 deg. .45' north latitudes. In this study, the natural radioactivity concentrations {sup 40}K, {sup 226}Ra and {sup 232}Th in some soil samples collected in Osmaniye have been investigated. The measurements have been performed using 3x3{sup ''} NaI(Tl) detector system.

  17. Accurate fast method with high chemical yield for determination of uranium isotopes (234U, 235U, 238U) in granitic samples using alpha spectroscopy

    NASA Astrophysics Data System (ADS)

    Guirguis, Laila A.; Farag, Nagdy M.; Salim, Adham K.

    2015-03-01

    The present study aims to use the α-spectroscopy at Nuclear Materials Authority (NMA) of Egypt. A radiochemical technique for analysis uranium isotopes was carried out for ten mineralized granitic samples together with the International standards RGU-1 (IAEA) and St4 (NMA). Several steps of sample preparation, radiochemical separation and source preparation were performed before analysis. Uranium was separated from sample matrix with 0.2 M TOPO in cyclohexane as an extracting agent with a chemical yield 98.95% then uranium was purified from lanthanides and actinides present with 0.2 M TOA in xylene as an extracting agent. The pure fraction was electrodeposited on a mirror-polished copper disc from buffer solution (NaHSO4+H2SO4+NH4OH). Rectangle pt-electrode with an anode-cathode distance of 2 cm was used. Current was 900 mA and the electrodeposition time reach up to 120 min. The achieved results show that the chemical yield ranged between 87.9±6.8 and 98±8.6.

  18. Uptake and kinetics of /sup 226/Ra, /sup 210/Pb and /sup 210/Po in big sagebrush. [Artemisia tridentata

    SciTech Connect

    Simon, S.L.

    1985-01-01

    Root uptake of /sup 226/Ra, /sup 210/Pb and /sup 210/Po by mature sagebrush was studied using a soil injection method for spiking the soil with minimal root disturbance. The main objective was to measure vegetation concentrations and determine concentration ratios (CR's) due to root uptake as a function of time in mature big sagebrush. Concentration ratios obtained in mature vegetation and in steady-state situations may be valuable in assessing the impact of uranium mining and milling. The vegetation was sampled approximately every 3 months for a 2 year period. Significant levels of activity were detected in the vegetation beginning at the first sampling (81 days after soil injection for /sup 226/Ra, 28 days for /sup 210/Pb and /sup 210/Po). There was an exponential decrease in concentration to an apparent steady-state value. Mean values (geometric) of the data pooled over the second year period indicated that the steady-state CR's for /sup 226/Ra, /sup 210/Pb and /sup 210/Po, as determined in mature sagebrush, were 0.04, 0.009, and 0.08, respectively. A three compartment mathematical model was formulated to help understand mechanisms of plant uptake and to predict, if possible, the concentration of /sup 226/Ra, /sup 210/Pb and /sup 210/Po in vegetation as a function of time after soil spiking. A numerical solution was determined by 'calibrating' the general model solution with constants determined from regressions of concentrations in vegetation, soil leaching and leaf leaching data. Validation of the model is currently not possible because of an absence of similar time-dependent uptake studies. 168 refs., 19 figs., 18 tabs.

  19. [About the contents of 40K, 226Ra and 232Th in forest soils of the Republic of Belarus].

    PubMed

    Perevolotskiĭ, A N; Perevolotskaia, T V

    2014-01-01

    The specific activity of 40K, 232Th and 226Ra in forest soil ecotopes (A2-B2-C2-D2) has been investigated. When the fertility of the soil increases from A2 to D2, then the specific activity of 40K increases in the rooting zone of the soil from 275 ± 6.9 up to 499 ± 11 Bq/kg, 232Th--from 11.8 ± 0.5 to 17.1 ± 1.1 Bq/kg, 226Ra- from 19.2 γ 0.8 to 27.9 ± 1.5 Bq/kg. The calculated capacity of the absorbed dose of γ-radiation conditioned by 40K, 232Th and 226Ra increases from A2 to D2 from 27.5 ± 0.5 to 44.1 ± 1.1 nGy / h at the height of 1 m.

  20. High-Resolution Inductively Coupled Plasma Optical Emission Spectrometry for (234)U/(238)Pu Age Dating of Plutonium Materials and Comparison to Sector Field Inductively Coupled Plasma Mass Spectrometry.

    PubMed

    Krachler, Michael; Alvarez-Sarandes, Rafael; Rasmussen, Gert

    2016-09-06

    Employing a commercial high-resolution inductively coupled plasma optical emission spectrometry (HR-ICP-OES) instrument, an innovative analytical procedure for the accurate determination of the production age of various Pu materials (Pu powder, cardiac pacemaker battery, (242)Cm heat source, etc.) was developed and validated. This undertaking was based on the fact that the α decay of (238)Pu present in the investigated samples produced (234)U and both mother and daughter could be identified unequivocally using HR-ICP-OES. Benefiting from the high spectral resolution of the instrument (<5 pm) and the isotope shift of the emission lines of both nuclides, (234)U and (238)Pu were selectively and directly determined in the dissolved samples, i.e., without a chemical separation of the two analytes from each other. Exact emission wavelengths as well as emission spectra of (234)U centered around λ = 411.590 nm and λ = 424.408 nm are reported here for the first time. Emission spectra of the isotopic standard reference material IRMM-199, comprising about one-third each of (233)U, (235)U, and (238)U, confirmed the presence of (234)U in the investigated samples. For the assessment of the (234)U/(238)Pu amount ratio, the emission signals of (234)U and (238)Pu were quantified at λ = 424.408 nm and λ = 402.148 nm, respectively. The age of the investigated samples (range: 26.7-44.4 years) was subsequently calculated using the (234)U/(238)Pu chronometer. HR-ICP-OES results were crossed-validated through sector field inductively coupled plasma mass spectrometry (SF-ICPMS) analysis of the (234)U/(238)Pu amount ratio of all samples applying isotope dilution combined with chromatographic separation of U and Pu. Available information on the assumed ages of the analyzed samples was consistent with the ages obtained via the HR-ICP-OES approach. Being based on a different physical detection principle, HR-ICP-OES provides an alternative strategy to the well-established mass

  1. Seasonal changes in submarine groundwater discharge to coastal salt ponds estimated using 226Ra and 228Ra as tracers

    USGS Publications Warehouse

    Hougham, A.L.; Moran, S.B.; Masterson, J.P.; Kelly, R.P.

    2008-01-01

    Submarine groundwater discharge (SGD) to coastal southern Rhode Island was estimated from measurements of the naturally-occurring radioisotopes 226Ra (t1/2 = 1600??y) and 228Ra (t1/2 = 5.75??y). Surface water and porewater samples were collected quarterly in Winnapaug, Quonochontaug, Ninigret, Green Hill, and Pt. Judith-Potter Ponds, as well as nearly monthly in the surface water of Rhode Island Sound, from January 2002 to August 2003; additional porewater samples were collected in August 2005. Surface water activities ranged from 12-83??dpm 100??L- 1 (60??dpm = 1??Bq) and 21-256??dpm 100??L- 1 for 226Ra and 228Ra, respectively. Porewater 226Ra activities ranged from 16-736??dpm 100??L- 1 (2002-2003) and 95-815??dpm 100??L- 1 (2005), while porewater 228Ra activities ranged from 23-1265??dpm 100??L- 1. Combining these data with a simple box model provided average 226Ra-based submarine groundwater fluxes ranging from 11-159??L m- 2 d- 1 and average 228Ra-derived fluxes of 15-259??L m- 2 d- 1. Seasonal changes in Ra-derived SGD were apparent in all ponds as well as between ponds, with SGD values of 30-472??L m- 2 d- 1 (Winnapaug Pond), 6-20??L m- 2 d- 1 (Quonochontaug Pond), 36-273??L m- 2 d- 1 (Ninigret Pond), 29-76??L m- 2 d- 1 (Green Hill Pond), and 19-83??L m- 2 d- 1 (Pt. Judith-Potter Pond). These Ra-derived fluxes are up to two orders of magnitude higher than results predicted by a numerical model of groundwater flow, estimates of aquifer recharge for the study period, and values published in previous Ra-based SGD studies in Rhode Island. This disparity may result from differences in the type of flow (recirculated seawater versus fresh groundwater) determined using each technique, as well as variability in porewater Ra activity. ?? 2007 Elsevier B.V. All rights reserved.

  2. {sup 40}K, {sup 115}Cs and {sup 226}Ra Soil and Plant Content in Seminatural Grasslands of Central Argentina

    SciTech Connect

    Ayub, J. Juri; Velasco, R. H.; Rizzotto, M.; Quintana, E.; Aguiar, J.

    2008-08-07

    Activity concentrations of {sup 40}K, {sup 226}Ra and {sup 137}Cs have been analyzed in soil and plant samples, collected in permanent grassland in central Argentina. Two near areas (A1 and A2) under field conditions with soil undisturbed at least in the last four decades were selected. For each of the three studied radionuclides we do not find differences in the inventories between both areas. The inventories range from 143 kBq m{sup -2} to 197 kBq m{sup -2} for {sup 40}K and from 13 kBq m{sup -2} to 18 kBq m{sup -2} for {sup 226}Ra. The vertical distributions of {sup 40}K and {sup 226}Ra are uniform through de soil profile. For {sup 137}Cs the inventories range from 0.33 kBq m{sup -2} to 0.73 kBq m{sup -2}. In spite of {sup 137}Cs inventories are similar in both areas the distribution through vertical profile is different. {sup 137}Cs activity concentration has a maximum for layers 5-10 cm depth in A1 and 10-15 cm depth in A2. For deeper layers both areas show similar activity concentrations. The diffusion coefficient (D{sub s}) and convection velocity (v{sub s}) are estimated with a convection-diffusion model. D{sub s} values are in the range reported in the bibliography, while v{sub s} values are one order of magnitude higher. After 40 years most {sup 137}Cs fallout is still in the layer 10-15 cm depth. The great penetration of {sup 137}Cs (25 cm) in these soils may be the result of a high sand and low fine materials content. {sup 137}Cs and {sup 226}Ra were not detected in grass samples. Activity concentration of {sup 40}K in vegetal samples ranges from 116 Bq kg{sup -1} to 613 Bq kg{sup -1}. The TF values obtained for {sup 40}K show a lognormal distribution and ranges from 0.05 to 0.42.

  3. Neutron Capture Cross Sections of 236U and 234U

    SciTech Connect

    Rundberg, R. S.; Bredeweg, T. A.; Bond, E. M.; Haight, R. C.; Hunt, L. F.; O'Donnell, J. M.; Schwantes, J. M.; Ullmann, J. L.; Vieira, D. J.; Wilhelmy, J. B.; Wouters, J. M.; Kronenberg, A.

    2006-03-13

    Accurate neutron capture cross sections of the actinide elements at neutron energies up to 1 MeV are needed to better interpret archived nuclear test data, for post-detonation nuclear attribution, and the Advanced Fuel Cycle Initiative. The Detector for Advance Neutron Capture Experiments, DANCE, has unique capabilities that allow the differentiation of capture gamma rays from fission gamma rays and background gamma rays from scattered neutrons captured by barium isotopes in the barium fluoride scintillators. The DANCE array has a high granularity, 160 scintillators, high efficiency, and nearly 4-{pi} solid angle. Through the use of cuts in cluster multiplicity and calorimetric energy the capture gamma-rays are differentiated from other sources of gamma rays. The preliminary results for the capture cross sections of 236U are in agreement with the ENDF/B-VI evaluation. The preliminary results for 234U lower are than ENDF/B-VI evaluation and are closer to older evaluations.

  4. 238U-230Th-226Ra disequilibria in dacite and plagioclase from the 2004-2005 eruption of Mount St. Helens: Chapter 36 in A volcano rekindled: the renewed eruption of Mount St. Helens, 2004-2006

    USGS Publications Warehouse

    Cooper, Kari M.; Donnelly, Carrie T.; Sherrod, David R.; Scott, William E.; Stauffer, Peter H.

    2008-01-01

    230Th)/(232Th) measured for the 1980s reference suite. However, (230Th)/(232Th) for plagioclase separates for dome samples erupted during October and November 2004 are significantly different from corresponding whole-rock values, which suggests that a large fraction (>30 percent) of crystals in each sample are foreign to the host liquid. Furthermore, plagioclase in the two 2004 samples have U-series characteristics distinct from each other and from plagioclase in dacite erupted in 1982, indicating that (1) the current eruption must include a component of crystals (and potentially associated magma) that were not sampled by the 1980-86 eruption, and (2) dacite magmas erupted only a month apart in 2004 contain different populations of crystals, indicating that this foreign component is highly heterogeneous within the 2004-5 magma reservoir.

  5. Theoretical studies of {sup 238}U-{sup 230}Th-{sup 226}Ra and {sup 235}U-{sup 231}Pa disequilibria in young lavas produced by mantle melting

    SciTech Connect

    Zou, H.; Zindler, A.

    2000-05-01

    This paper provides ready-to-use equations to describe variations in uranium-series (U-series) disequilibrium as a function of elemental distribution coefficients, melting porosity, melting rate, and melting time. The effects of these melting parameters on U-series disequilibria are quantitatively evaluated in both an absolute and relative sense. The importance of net elemental fractionation and ingrowth of daughter nuclides are also described and compared in terms of their relative contributions to total U-series disequilibrium. In addition, the authors compare the production of U-series disequilibrium during mantle melting to trace element fractionations produced by melting in a similar context. Trace element fractionations depend externally on the degree to which a source is melted, whereas U-series disequilibrium depends upon both the degree and rate of melting. In contrast to previous models, their approach to modeling U-series disequilibrium during dynamic melting collapses simply to a description of trace element behavior during dynamic melting when the appropriate decay terms are omitted. Their formulation shows that extremely small degrees of melting, sometimes called upon to explain observed extents of U-series disequilibrium, are not always required.

  6. (226)Ra dynamic lixiviation from phosphogypsum samples by an automatic flow-through system with integrated renewable solid-phase extraction.

    PubMed

    Ceballos, Melisa Rodas; Borràs, Antoni; García-Tenorio, Rafael; Rodríguez, Rogelio; Estela, José Manuel; Cerdà, Víctor; Ferrer, Laura

    2017-05-15

    The release of (226)Ra from phosphogypsum (PG) was evaluated by developing a novel tool for fully automated (226)Ra lixiviation from PG integrating extraction/pre-concentration using a renewable sorbent format. Eight leached fractions (30mL each one) and a residual fraction were analyzed allowing the evaluation of dynamic lixiviation of (226)Ra. An automatic system allows this approach coupling a homemade cell with a (226)Ra extraction/pre-concentration method, which is carried out combining two procedures: Ra adsorption on MnO2 and its posterior co-precipitation with BaSO4. Detection was carried out with a low-background proportional counter, obtaining a minimum detectable activity of 7Bqkg(-1). Method was validated by analysis of a PG reference material (MatControl CSN-CIEMAT 2008), comparing the content found in fractions (sum of leached fractions + residual fraction) to the reference value. PG samples from Huelva (Spain) were studied. (226)Ra average activity concentration of the sum of leached fractions with artificial rainwater at pH 5.4±0.2 was 105±3Bqkg(-1)d.w. representing a (226)Ra lixiviation of 37%; while at pH 2.0±0.2, it was 168±3Bqkg(-1) d.w., which represents a 50%. Also, static lixiviation, maintaining the same experimental conditions, was carried out indicating that, for both considered pH, the (226)Ra release from PG is up to 50% higher in a dynamic leaching that in a static one, may have both environmental and reutilization implications.

  7. Soil features and indoor radon concentration prediction: radon in soil gas, pedology, permeability and 226Ra content.

    PubMed

    Lara, E; Rocha, Z; Santos, T O; Rios, F J; Oliveira, A H

    2015-11-01

    This work aims at relating some physicochemical features of soils and their use as a tool for prediction of indoor radon concentrations of the Metropolitan Region of Belo Horizonte (RMBH), Minas Gerais, Brazil. The measurements of soil gas radon concentrations were performed by using an AlphaGUARD monitor. The (226)Ra content analysis was performed by gamma spectrometry (high pure germanium) and permeabilities were performed by using the RADON-JOK permeameter. The GEORP indicator and soil radon index (RI) were also calculated. Approximately 53 % of the Perferric Red Latosols measurement site could be classified as 'high risk' (Swedish criteria). The Litholic Neosols presented the lowest radon concentration mean in soil gas. The Perferric Red Latosols presented significantly high radon concentration mean in soil gas (60.6 ± 8.7 kBq m(-3)), high indoor radon concentration, high RI, (226)Ra content and GEORP. The preliminary results may indicate an influence of iron formations present very close to the Perferric Red Latosols in the retention of uranium minerals.

  8. Interaction times in the {sup 136}Xe+{sup 136}Xe and {sup 238}U+{sup 238}U reactions with a quantum master equation

    SciTech Connect

    Sargsyan, V. V.; Kanokov, Z.; Adamian, G. G.; Antonenko, N. V.; Scheid, W.

    2009-10-15

    Using the reduced-density-matrix formalism, the interaction time of two heavy nuclei is studied. In the reactions {sup 136}Xe+{sup 136}Xe and {sup 238}U+{sup 238}U, the mean interaction time and variance of interaction time distribution are calculated and compared with those of other treatments.

  9. {sup 226}Ra and {sup 231}Pa systematics of axial MORB, crustal residence ages, and magma chamber characteristics at 9--10{degree}N East Pacific Rise

    SciTech Connect

    Goldstein, S.J.; Murrell, M.T.; Perfit, M.R.; Batiza, R.; Fornari, D.J.

    1994-06-01

    Mass spectrometric measurements of {sup 30}Th-22{sup 226}Ra and {sup 235}-U{sup 231}Pa disequilibria for axial basalts are used to determine crustal residence ages for MORB magma and investigate the temporal and spatial characteristics of axial magma chambers (AMC) at 9--10{degrees}N East Pacific Rise (EPR). Relative crustal residence ages can be calculated from variations in {sup 226}Ra/{sup 230}Th and {sup 231}Pa/{sup 235}U activity ratios for axial lavas, if (1) mantle sources and melting are uniform, and mantle transfer times are constant or rapid for axial N-MORB, and (2) {sup 231}Pa/{sup 235}U and {sup 226}Ra/{sup 230}Th in the melt are unaffected by shallow level fractional crystallization. Uniform Th, Sr, and Nd isotopic systematics and incompatible element ratios for N-MORB along the 9--10{degrees}N segment indicate that mantle sources and transfer times are similar. In addition, estimated bulk solid/melt partition coefficients for U, Th, and Pa are small, hence effects of fractional crystallization on {sup 231}Pa/{sup 235}U ratios for the melt are expected to be negligible. However, fractional crystallization of plagioclase in the AMC would lower {sup 226}Ra/{sup 230}Th ratios in the melt and produce a positive bias in {sup 226}Ra crustal residence ages for fractionated lavas.

  10. The Enhancement of 226Ra in a Tidal Estuary due to the Operation of Fertilizer Factories and Redissolution from Sediments: Experimental Results and a Modelling Study

    NASA Astrophysics Data System (ADS)

    Periáñez, R.

    2002-05-01

    The presence of 226Ra in a tidal estuary formerly affected by direct discharges from a phosphate fertilizer complex has been investigated. In general, activity levels are lower than those detected when direct discharges were carried out. However, there is still a clear contamination that can be attributed, presumably, to the disposal of Ra-containing phosphogypsum to the river and to the redissolution of radionuclides from the contaminated sediments. A numerical model of the estuary has been developed to investigate these hypothesis. The hydrodynamics are first calibrated and standard tidal analysis is carried out. The dispersion model computes instantaneous currents from the so obtained tidal constants to speed up simulations. The exchanges of 226Ra between water and the bottom sediment have been described in terms of kinetic transfer coefficients. Model results are, in general, in agreement with observations. The simulation results support the previous idea of sediments acting as a source of 226Ra to the water column.

  11. Magma differentiation rates from ( 226Ra / 230Th) and the size and power output of magma chambers

    NASA Astrophysics Data System (ADS)

    Blake, Stephen; Rogers, Nick

    2005-08-01

    We present a mathematical model for the evolution of the ( 226Ra / 230Th) activity ratio during simultaneous fractional crystallization and ageing of magma. The model is applied to published data for four volcanic suites that are independently known to have evolved by fractional crystallization. These are tholeiitic basalt from Ardoukoba, Djibouti, MORB from the East Pacific Rise, alkali basalt to mugearite from Vestmannaeyjar, Iceland, and basaltic andesites from Miyakejima, Izu-Bonin arc. In all cases ( 226Ra / 230Th) correlates with indices of fractional crystallization, such as Th, and the data fall close to model curves of constant fractional crystallization rate. The best fit rates vary from 2 to 6 × 10 - 4 yr - 1 . Consequently, the time required to generate moderately evolved magmas ( F ≤ 0.7) is of the order of 500 to 1500 yrs and closed magma chambers will have lifetimes of 1700 to 5000 yrs. These rates and timescales are argued to depend principally on the specific power output (i.e., power output per unit volume) of the magma chambers that are the sites of fractional crystallization. Equating the heat flux at the EPR to the heat flux from the sub-axial magma chamber that evolves at a rate of ca. 3 × 10 - 4 yr - 1 implies that the magma body is a sill of ca. 100 m thickness, a value which coincides with independent estimates from seismology. The similarity of the four inferred differentiation rates suggests that the specific power output of shallow magma chambers in a range of tectonic settings covers a similarly narrow range of ca. 10 to 50 MW km - 3 . Their differentiation rates are some two orders of magnitude slower than that of the basaltic Makaopuhi lava lake, Hawaii, that cooled to the atmosphere. This is consistent with the two orders of magnitude difference in heat flux between Makaopuhi and the East Pacific Rise. ( 226Ra / 230Th) data for magma suites related by fractional crystallization allow the magma differentiation rate to be estimated

  12. Potential human health risk by 234,238U and 210Po due to consumption of fish from the "Luis L. Leon" reservoir (Northern Mexico)

    NASA Astrophysics Data System (ADS)

    Luna-Porres, M. Y.; Rodríguez-Villa, M. A.; Herrera-Peraza, E.; Cabral-Lares, M.; Renteria-Villalobos, M.; Montero-Cabrera, M. E.

    2014-07-01

    The Conchos River is one of the most important in northern Mexico and the main surface waterway in the arid state of Chihuahua. The Luis L. Leon dam produces the Luis L. Leon Reservoir, which is the last major reservoir before the Conchos River enters the Rio Grande at the Texas-Chihuahua border. Activity concentrations (AC) of 234,238U and 210Po in fillet and liver of three stocked fish species (Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus), as well as in water from the Luis L. Leon reservoir were determined. 238U and 234U ACs in fillet samples showed values of 0.007-0.014 and 0.01-0.02 Bq kg-1 wet weight (ww), respectively. Liver samples for Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus species, present 210Po AC of 1.16-3.26 0.70-1.13 and 0.93-1.37 Bqṡkg-1 ww. The elemental Bioaccumulation Factor (BAF) for fish tissues respect to their concentrations in water was determined. Lepomis cyanellus species showed the highest BAF for total uranium in fillet, with value 1.5. The annual effective dose for uranium in adults by fish consumption in this work ranged from 4.46×10-3 to 3.68×10-2 μSvṡyear-1. The difference in concentrations of uranium in fillet among the studied species is likely primarily due to their differences in diet and habitat.

  13. Radionuclide ((226)Ra, (232)Th, (40)K) accumulation among plant species in mangrove ecosystems of Pattani Bay, Thailand.

    PubMed

    Kaewtubtim, Pungtip; Meeinkuirt, Weeradej; Seepom, Sumalee; Pichtel, John

    2017-02-15

    Little is known regarding phytoremediation of radionuclides from soil; even less is known about radionuclide contamination and removal in tropical ecosystems such as mangrove forests. In mangrove forests in Pattani Bay, Thailand, 18 plant species from 17 genera were evaluated for radionuclide concentrations within selected plant parts. Two shrub species, Avicennia marina and Pluchea indica, accumulated the highest (232)Th (24.6Bqkg(-1)) and (40)K (220.7Bqkg(-1)) activity concentrations in roots, respectively. Furthermore, the aquatic species Typha angustifolia accumulated highest (232)Th, (40)K and (226)Ra activity concentrations (85.2, 363.5, 16.6Bqkg(-1), respectively) with the highest transfer factors (TFs) (3.0, 2.0, 5.9, respectively) in leaves. Leaves of T. angustifolia had an absorbed dose rate in air (D) over the recommended value (74.8nGyh(-1)) that was considered sufficiently high to be of concern for human consumption.

  14. Reaction rate calibration techniques at ZPPR for /sup 239/Pu fission, /sup 235/U fission, /sup 238/U fission, and /sup 238/U capture

    SciTech Connect

    Brumbach, S.B.; Maddison, D.W.

    1982-06-10

    Reaction-rate calibration techniques used at ZPPR are described for /sup 239/Pu fission, /sup 235/U fission, /sup 238/U fission and /sup 238/U capture. In addition to these absolute reaction rates, calibration techniques are described for fission-rate ratios and the ratio of /sup 238/U capture to /sup 239/U capture to /sup 239/Pu fission. Uncertainty estimates are presented for all calibrations. Intercomparison measurements are reported which support the validity of the calibration techniques and their estimated uncertainties.

  15. Heavy actinide cross sections in the /sup 238/U + /sup 248/Cm reaction

    SciTech Connect

    Kratz, J V; Bruechle, W; Gaeggeler, H

    1981-01-01

    Cross sections for the production of Cf, Es, Fm, and Md isotopes in the reactions of 7.4 MeV/u /sup 238/U-ions with /sup 248/Cm targets are presented and discussed. Cross sections for the formation of heavy actinides in the reactions of 7.5 MeV/u /sup 136/Xe and /sup 238/U-projectiles with /sup 238/U-targets are presented for comparison. (WHK)

  16. (226) RA AND (228) RA ACTIVITIES ASSOCIATED WITH AGRICULTURAL DRAINAGE PONDS AND WETLAND PONDS IN THE KANKAKEE WATERSHED, IL-IN, USA

    EPA Science Inventory

    Background radioactivity is elevated in many agricultural drainage ponds and also constructed wetland ponds in the Kankakee watershed. During 1995-1999, gross-a and -B activities were measured up to 455 and 1650 mBq L-1, respectively. 226Ra and 228Ra averaged 139 and 192 mBq L-01...

  17. Precise determination of photon emission probabilities for the main X- and gamma-rays of 226Ra in equilibrium with daughters.

    PubMed

    Morel, J; Sepman, S; Rasko, M; Terechtchenko, E; Delgado, J U

    2004-01-01

    Within the context of a joint project between VNIIM (D.I. Mendeleyev Institute for Metrology) and LNHB (Laboratoire National Henri Becquerel), special 226Ra sources were prepared by VNIIM in order to determine as accurately as possible the absolute photon emission probabilities for the main X- and gamma-rays following the decay of 226Ra and daughters. The main purpose of this work was to supplement a previous joint study by Laboratorio Nacional de Metrologia das Radiaçoes Ionizantes (LNMRI) and LNHB to determine their relative values. Some specific point sources were produced for alpha-spectrometry measurements that were undertaken at VNIIM and also for gamma-ray spectrometry studies at VNIIM and LNHB. The 226Ra activity for the gamma-spectrometric sources was measured relative to the alpha-spectrometric sources by comparing the counts of the main gamma-rays. The total uncertainty of the activity for these sources was 0.2% (k = 1). Using calibrated germanium detectors, several X- and gamma-ray spectra were analyzed to determine the absolute photon emission probabilities of 226Ra in radioactive equilibrium with daughters. The results are presented and compared to other published values.

  18. Effect of low molecular weight organic acids on the uptake of (226)Ra by corn (Zea mays L.) in a region of high natural radioactivity in Ramsar-Iran.

    PubMed

    Nezami, Sareh; Malakouti, Mohammad Jafar; Bahrami Samani, Ali; Ghannadi Maragheh, Mohammad

    2016-11-01

    To study the benefit of including citric and oxalic acid treatments for phytoremediation of (226)Ra contaminated soils a greenhouse experiment with corn was conducted. A soil was sampled from a region of high natural (226)Ra radioactivity in Ramsar, Iran. After cultivation of corn seed and using organic acid treatments at 1, 10 and 100 mM concentrations, plants (shoots and roots) were harvested, digested and prepared to measure (226)Ra activity. Simultaneously, sequential selective extraction were performed to estimate the partitioning of (226)Ra among geochemical extraction. Results showed that the maximum uptake of (226)Ra in plants was observed in citric acid (6.3%) and then oxalic acid (6%) at 100 mM concentration. These treatments increased radium uptake by a factor of 1.5 than the control. Enhancement of radium uptake by plants was related to soil pH reduction of organic acids in comparison to control. Also, the maximum uptake of this radionuclide in all treatments was obtained in roots compared to shoots. (226)Ra fractionations results revealed that 91.8% of radium was in the residual phase of the soil and the available fractions were less than 2%. As the main percent of (226)Ra was in the residual phase of the soil in this region, it seems that organic acids had not significant effect on the uptake of (226)Ra for phytoremediation by corn in this condition.

  19. Elastic and inelastic scattering of neutrons on 238U nucleus

    NASA Astrophysics Data System (ADS)

    Capote, R.; Trkov, A.; Sin, M.; Herman, M. W.; Soukhovitskiĩ, E. Sh.

    2014-04-01

    Advanced modelling of neutron induced reactions on the 238U nucleus is aimed at improving our knowledge of neutron scattering. Capture and fission channels are well constrained by available experimental data and neutron standard evaluation. A focus of this contribution is on elastic and inelastic scattering cross sections. The employed nuclear reaction model includes - a new rotational-vibrational dispersive optical model potential coupling the low-lying collective bands of vibrational character observed in even-even actinides; - the Engelbrecht-Weidenmüller transformation allowing for inclusion of compound-direct interference effects; - and a multi-humped fission barrier with absorption in the secondary well described within the optical model for fission. Impact of the advanced modelling on elastic and inelastic scattering cross sections including angular distributions and emission spectra is assessed both by comparison with selected microscopic experimental data and integral criticality benchmarks including measured reaction rates (e.g. JEMIMA, FLAPTOP and BIG TEN). Benchmark calculations provided feedback to improve the reaction modelling. Improvement of existing libraries will be discussed.

  20. Experimental study of the {sup 238}U({sup 36}S,3-5n){sup 269-271}Hs reaction leading to the observation of {sup 270}Hs

    SciTech Connect

    Graeger, R.; Gorshkov, A.; Tuerler, A.; Yakushev, A.; Ackermann, D.; Duellmann, Ch. E.; Hessberger, F. P.; Huebner, A.; Jaeger, E.; Khuyagbaatar, J.; Kindler, B.; Krier, J.; Lommel, B.; Schaedel, M.; Schausten, B.; Chelnokov, M.; Chepigin, V.; Kuznetsov, A.; Petrushkin, O.; Dvorak, J.

    2010-06-15

    The deformed doubly magic nucleus {sup 270}Hs has so far only been observed as the four-neutron (4n) evaporation residue of the reaction {sup 26}Mg+{sup 248}Cm, where a maximum cross section of 3 pb was measured. Theoretical studies on the formation of {sup 270}Hs in the 4n evaporation channel of fusion reactions with different entrance channel asymmetry in the framework of a two-parameter Smoluchowski equation predict that the reactions {sup 48}Ca+{sup 226}Ra and {sup 36}S+{sup 238}U result in higher cross sections due to lower reaction Q values, in contrast to simple arguments based on the reaction asymmetry, which predict opposite trends. Calculations using hivap predict cross sections for the reaction {sup 36}S+{sup 238}U that are similar to those of the {sup 26}Mg+{sup 248}Cm reaction. Here, we report on the first measurement of evaporation residues formed in the complete nuclear fusion reaction {sup 36}S+{sup 238}U and the observation of {sup 270}Hs, which is produced in the 4n evaporation channel, with a measured cross section of 0.8{sub -0.7}{sup +2.6} pb at 51-MeV excitation energy. The one-event cross-section limits (68% confidence level) for the 3n, 4n, and 5n evaporation channels at 39-MeV excitation energy are 2.9 pb, while the cross-section limits of the 3n and 5n channel at 51 MeV are 1.5 pb. This is significantly lower than the 5n cross section of the {sup 26}Mg+{sup 248}Cm reaction at similar excitation energy.

  1. Laser-trapping of {sup 225}Ra and {sup 226}Ra with repumping by room-temperature blackbody radiation.

    SciTech Connect

    Guest, J. R.; Scielzo, N. D.; Ahmad, I.; Bailey, K.; Greene, J. P.; Holt, R. J.; Lu, Z.-T.; O'Connor, T. P.; Potterveld, D. H.; Physics; Enrico Fermi Inst.; Univ. of Chicago

    2007-02-27

    We have demonstrated Zeeman slowing and capture of neutral {sup 225}Ra and {sup 226}Ra atoms in a magneto-optical trap. The intercombination transition {sup 1}S{sub 0} {yields} {sup 3}P{sub 1} is the only quasicycling transition in radium and was used for laser-cooling and trapping. Repumping along the {sup 3}D{sub 1} {yields} {sup 1}P{sub 1} transition extended the lifetime of the trap from milliseconds to seconds. Room-temperature blackbody radiation was demonstrated to provide repumping from the metastable {sup 3}P{sub 0} level. We measured the isotope shift and hyperfine splittings on the {sup 3}D{sub 1} {yields} {sup 1}P{sub 1} transition with the laser-cooled atoms, and set a limit on the lifetime of the {sup 3}D{sub 1} level based on the measured blackbody repumping rate. Laser-cooled and trapped radium is an attractive system for studying fundamental symmetries.

  2. Vertical migration of 60Co, 137Cs and 226Ra in agricultural soils as observed in lysimeters under crop rotation.

    PubMed

    Shinonaga, T; Schimmack, W; Gerzabek, M H

    2005-01-01

    In most studies quantifying the migration parameters - apparent migration velocity and apparent dispersion coefficient - of radionuclides in the soil by model calculations, these parameters are determined for undisturbed soils. For soils disturbed by ploughing, however, no such data are available in the literature. Therefore, in the present study, the migration parameters of (137)Cs, (60)Co and (226)Ra were estimated for ploughed soils by means of a convection-dispersion model. The depth distributions of the radionuclides were determined in four lysimeters (area: 1m(2), depth of soil monolith: 0.75m) filled with artificially contaminated soils of different types in July 1990. The lysimeters were cropped with agricultural plants. The soil in each lysimeter was ploughed manually once a year until 1996 (plough depth 20cm). In July 1999, soil samples were collected from three pits in each lysimeter. The depth distributions of all radionuclides proved to be very similar in each soil pit. The spatial variability of the depth distributions of a given radionuclide within the lysimeters was about the same as their variability between the four lysimeters. Evaluation of the migration parameters revealed that the convective transport of the radionuclides was always rather small or even zero, while the dispersive transport caused a "melting" process of the initially sharp activity edge at the lower border of the Ap horizon. These results are explained by the high evapotranspiration (80-90% of the total precipitation plus irrigation) and the small amounts of seepage water during the observation period of 9 years.

  3. Mobile gamma-ray scanning system for detecting radiation anomalies associated with /sup 226/Ra-bearing materials

    SciTech Connect

    Myrick, T.E.; Blair, M.S.; Doane, R.W.; Goldsmith, W.A.

    1982-11-01

    A mobile gamma-ray scanning system has been developed by Oak Ridge National Laboratory for use in the Department of Energy's remedial action survey programs. The unit consists of a NaI(T1) detection system housed in a specially-equipped van. The system is operator controlled through an on-board mini-computer, with data output provided on the computer video screen, strip chart recorders, and an on-line printer. Data storage is provided by a floppy disk system. Multichannel analysis capabilities are included for qualitative radionuclide identification. A /sup 226/Ra-specific algorithm is employed to identify locations containing residual radium-bearing materials. This report presents the details of the system description, software development, and scanning methods utilized with the ORNL system. Laboratory calibration and field testing have established the system sensitivity, field of view, and other performance characteristics, the results of which are also presented. Documentation of the instrumentation and computer programs are included.

  4. 210Pb-226Ra chronology reveals rapid growth rate of Madrepora oculata and Lophelia pertusa on world's largest cold-water coral reef

    NASA Astrophysics Data System (ADS)

    Sabatier, P.; Reyss, J.-L.; Hall-Spencer, J. M.; Colin, C.; Frank, N.; Tisnérat-Laborde, N.; Bordier, L.; Douville, E.

    2012-03-01

    Here we show the use of the 210Pb-226Ra excess method to determine the growth rate of two corals from the world's largest known cold-water coral reef, Røst Reef, north of the Arctic circle off Norway. Colonies of each of the two species that build the reef, Lophelia pertusa and Madrepora oculata, were collected alive at 350 m depth using a submersible. Pb and Ra isotopes were measured along the major growth axis of both specimens using low level alpha and gamma spectrometry and trace element compositions were studied. 210Pb and 226Ra differ in the way they are incorporated into coral skeletons. Hence, to assess growth rates, we considered the exponential decrease of initially incorporated 210Pb, as well as the increase in 210Pb from the decay of 226Ra and contamination with 210Pb associated with Mn-Fe coatings that we were unable to remove completely from the oldest parts of the skeletons. 226Ra activity was similar in both coral species, so, assuming constant uptake of 210Pb through time, we used the 210Pb-226Ra chronology to calculate growth rates. The 45.5 cm long branch of M. oculata was 31 yr with an average linear growth rate of 14.4 ± 1.1 mm yr-1 (2.6 polyps per year). Despite cleaning, a correction for Mn-Fe oxide contamination was required for the oldest part of the colony; this correction corroborated our radiocarbon date of 40 yr and a mean growth rate of 2 polyps yr-1. This rate is similar to the one obtained in aquarium experiments under optimal growth conditions. For the 80 cm-long L. pertusa colony, metal-oxide contamination remained in both the middle and basal part of the coral skeleton despite cleaning, inhibiting similar age and growth rate estimates. The youngest part of the colony was free of metal oxides and this 15 cm section had an estimated a growth rate of 8 mm yr-1, with high uncertainty (~1 polyp every two to three years). We are less certain of this 210Pb growth rate estimate which is within the lowermost ranges of previous growth

  5. Geochronology and petrogenesis of MORB from the Juan de Fuca and Gorda ridges by 238U230Th disequilibrium

    USGS Publications Warehouse

    Goldstein, S.J.; Murrell, M.T.; Janecky, D.R.; Delaney, J.R.; Clague, D.A.

    1991-01-01

    A highly precise mass spectrometric method of analysis was used to determine 238U234U230Th232Th in axial and off-axis basalt glasses from Juan de Fuca (JDF) and Gorda ridges. Initial 230Th activity excesses in the axial samples range from 3 to 38%, but generally lie within a narrow range of 12 to 15%. Secondary alteration effects were evaluated using ??234U and appear to be negligible; hence the 230Th excesses are magmatic in origin. Direct dating of MORB was accomplished by measuring the decrease in excess 230Th in off-axis samples. 238U230Th ages progressively increase with distance from axis. Uncertainties in age range from 10 to 25 ka for UTh ages of 50 to 200 ka. The full spreading rate based on UTh ages for Endeavour segment of JDF is 5.9 ?? 1/2 cm/yr, with asymmetry in spreading between the Pacific (4.0 ?? 0.6 cm/yr) and JDF (1.9 ?? 0.6 cm/yr) plates. For northern Gorda ridge, the half spreading rate for the JDF plate is found to be 3.0 ?? 0.4 cm/yr. These rates are in agreement with paleomagnetic spreading rates and topographic constraints. This suggests that assumptions used to determine ages, including constancy of initial 230Th 232Th ratio over time, are generally valid for the areas studied. Samples located near the axis of spreading are typically younger than predicted by these spreading rates, which most likely reflects recent volcanism within a 1-3 km wide zone of crustal accretion. Initial 230Th/232Th ratios and 230Th activity were also used to examine the recent Th/U evolution and extent of melting of mantle sources beneath these ridges. A negative anomaly in 230Th 232Th for Axial seamount lavas provides the first geochemical evidence of a mantle plume source for Axial seamount and the Cobb-Eickelberg seamount chain and indicates recent depletion of other JDF segment sources. Large 230Th activity excesses for lavas from northern Gorda ridge and Endeavour segment indicate formation from a lower degree of partial melting than other segments. An

  6. Prospects of heavy and superheavy element production via inelastic nucleus-nucleus collisions - from 238U+238U to18O+254Es

    NASA Astrophysics Data System (ADS)

    Schädel, Matthias

    2016-12-01

    Multi-nucleon transfer reactions, frequently termed deep-inelastic, between heavy-ion projectiles and actinide targets provide prospects to synthesize unknown isotopes of heavy actinides and superheavy elements with neutron numbers beyond present limits. The 238U on 238U reaction, which revealed essential aspects of those nuclear reactions leading to surviving heavy nuclides, mainly produced in 3n and 4n evaporation channels, is discussed in detail. Positions and widths of isotope distributions are compared. It is shown, as a general rule, that cross sections peak at irradiation energies about 10% above the Coulomb barrier. Heavy target nuclei are essential for maximizing cross sections. Experimental results from the 238U on 248Cm reaction, including empirical extrapolations, are compared with theoretical model calculations predicting relatively high cross sections for neutron-rich nuclei. Experiments to test the validity of such predictions are proposed. Comparisons between rather symmetric heavy-ion reactions like 238U on 248Cm (or heavier targets up to 254Es) with very asymmetric ones like 18O on 254Es reveal that the ones with 238U as a projectile have the highest potential in the superheavy element region while the latter ones can be advantageous for the synthesis of heavy actinide isotopes. Concepts for highly efficient recoil separators designed for transfer products are presented.

  7. Measurement of (233)U/(234)U ratios in contaminated groundwater using alpha spectrometry.

    PubMed

    Harrison, Jennifer J; Payne, Timothy E; Wilsher, Kerry L; Thiruvoth, Sangeeth; Child, David P; Johansen, Mathew P; Hotchkis, Michael A C

    2016-01-01

    The uranium isotope (233)U is not usually observed in alpha spectra from environmental samples due to its low natural and fallout abundance. It may be present in samples from sites in the vicinity of nuclear operations such as reactors or fuel reprocessing facilities, radioactive waste disposal sites or sites affected by clandestine nuclear operations. On an alpha spectrum, the two most abundant alpha emissions of (233)U (4.784 MeV, 13.2%; and 4.824 MeV, 84.3%) will overlap with the (234)U doublet peak (4.722 MeV, 28.4%; and 4.775 MeV, 71.4%), if present, resulting in a combined (233+234)U multiplet. A technique for quantifying both (233)U and (234)U from alpha spectra was investigated. A series of groundwater samples were measured both by accelerator mass spectrometry (AMS) to determine (233)U/(234)U atom and activity ratios and by alpha spectrometry in order to establish a reliable (233)U estimation technique using alpha spectra. The Genie™ 2000 Alpha Analysis and Interactive Peak Fitting (IPF) software packages were used and it was found that IPF with identification of three peaks ((234)U minor, combined (234)U major and (233)U minor, and (233)U major) followed by interference correction on the combined peak and a weighted average activity calculation gave satisfactory agreement with the AMS data across the (233)U/(234)U activity ratio range (0.1-20) and (233)U activity range (2-300 mBq) investigated. Correlation between the AMS (233)U and alpha spectrometry (233)U was r(2) = 0.996 (n = 10).

  8. 226Ra, 232Th and 40K contents in water samples in part of central deserts in Iran and their potential radiological risk to human population

    PubMed Central

    2014-01-01

    Background The radiological quality of 226Ra, 232Th and 40K in some samples of water resources collected in Anarak-Khour a desertic area, Iran has been measured by direct gamma ray spectroscopy using high purity germanium detector in this paper. Result The concentration ranged from ≤0.5 to 9701 mBq/L for 226Ra; ≤0.2 to 28215 mBq/L for 232Th and < MDA to 10332 mBq/L for 40K. The radium equivalent activity was well below the defined limit of 370Bq/L. The calculated external hazard indices were found to be less than 1 which shows a low dose. Conclusion These results can be contributed to the database of this area because it may be used as disposal sites of nuclear waste in future. PMID:24883192

  9. Migration of the FDNPP-derived (134)Cs and (137)Cs along with (226)Ra and (228)Ra concentrations across the northwestern North Pacific Ocean.

    PubMed

    Inoue, M; Shirotani, Y; Nagao, S; Kofuji, H; Volkov, Y N; Nishioka, J

    2016-10-01

    We examined lateral distributions of (134)Cs, (137)Cs, (226)Ra, and (228)Ra in the surface seawaters around the Kuril Islands and the Kamchatka Peninsula in the northwestern North Pacific Ocean during June 2014. The sampling area included three water current areas, the Oyashio Current, the current from the Okhotsk Sea, and the coastal current along the east Kamchatka Peninsula. (226)Ra and (228)Ra distributions differed along the three currents. Low levels of (134)Cs were detected in the surface waters of the Oyashio Current (0.09-0.35 mBq/L), but it was <∼0.1 mBq/L at the surface along the other two currents. This indicates that the distribution of Fukushima Dai-ichi Nuclear Power Plant (FDNPP)-derived radiocesium in surface waters off the Kamchatka and along the Kuril Islands is predominantly governed by the Oyashio current system.

  10. Mapping the spatial distribution and activity of (226)Ra at legacy sites through Machine Learning interpretation of gamma-ray spectrometry data.

    PubMed

    Varley, Adam; Tyler, Andrew; Smith, Leslie; Dale, Paul; Davies, Mike

    2016-03-01

    Radium ((226)Ra) contamination derived from military, industrial, and pharmaceutical products can be found at a number of historical sites across the world posing a risk to human health. The analysis of spectral data derived using gamma-ray spectrometry can offer a powerful tool to rapidly estimate and map the activity, depth, and lateral distribution of (226)Ra contamination covering an extensive area. Subsequently, reliable risk assessments can be developed for individual sites in a fraction of the timeframe compared to traditional labour-intensive sampling techniques: for example soil coring. However, local heterogeneity of the natural background, statistical counting uncertainty, and non-linear source response are confounding problems associated with gamma-ray spectral analysis. This is particularly challenging, when attempting to deal with enhanced concentrations of a naturally occurring radionuclide such as (226)Ra. As a result, conventional surveys tend to attribute the highest activities to the largest total signal received by a detector (Gross counts): an assumption that tends to neglect higher activities at depth. To overcome these limitations, a methodology was developed making use of Monte Carlo simulations, Principal Component Analysis and Machine Learning based algorithms to derive depth and activity estimates for (226)Ra contamination. The approach was applied on spectra taken using two gamma-ray detectors (Lanthanum Bromide and Sodium Iodide), with the aim of identifying an optimised combination of detector and spectral processing routine. It was confirmed that, through a combination of Neural Networks and Lanthanum Bromide, the most accurate depth and activity estimates could be found. The advantage of the method was demonstrated by mapping depth and activity estimates at a case study site in Scotland. There the method identified significantly higher activity (<3 Bq g(-1)) occurring at depth (>0.4m), that conventional gross counting algorithms

  11. Tracking suspended particle transport via radium isotopes ((226)Ra and (228)Ra) through the Apalachicola-Chattahoochee-Flint River system.

    PubMed

    Peterson, Richard N; Burnett, William C; Opsahl, Stephen P; Santos, Isaac R; Misra, Sambuddha; Froelich, Philip N

    2013-02-01

    Suspended particles in rivers can carry metals, nutrients, and pollutants downstream which can become bioactive in estuaries and coastal marine waters. In river systems with multiple sources of both suspended particles and contamination sources, it is important to assess the hydrologic conditions under which contaminated particles can be delivered to downstream ecosystems. The Apalachicola-Chattahoochee-Flint (ACF) River system in the southeastern United States represents an ideal system to study these hydrologic impacts on particle transport through a heavily-impacted river (the Chattahoochee River) and one much less impacted by anthropogenic activities (the Flint River). We demonstrate here the utility of natural radioisotopes as tracers of suspended particles through the ACF system, where particles contaminated with arsenic (As) and antimony (Sb) have been shown to be contributed from coal-fired power plants along the Chattahoochee River, and have elevated concentrations in the surficial sediments of the Apalachicola Bay Delta. Radium isotopes ((228)Ra and (226)Ra) on suspended particles should vary throughout the different geologic provinces of this river system, allowing differentiation of the relative contributions of the Chattahoochee and Flint Rivers to the suspended load delivered to Lake Seminole, the Apalachicola River, and ultimately to Apalachicola Bay. We also use various geochemical proxies ((40)K, organic carbon, and calcium) to assess the relative composition of suspended particles (lithogenic, organic, and carbonate fractions, respectively) under a range of hydrologic conditions. During low (base) flow conditions, the Flint River contributed 70% of the suspended particle load to both the Apalachicola River and the bay, whereas the Chattahoochee River became the dominant source during higher discharge, contributing 80% of the suspended load to the Apalachicola River and 62% of the particles entering the estuary. Neither of these hydrologic

  12. 226Ra and other radionuclides in water, vegetation, and tissues of beavers (Castor canadensis) from a watershed containing U tailings near Elliot Lake, Canada.

    PubMed

    Clulow, F V; Mirka, M A; Davé, N K; Lim, T P

    1991-01-01

    Radionuclide levels were measured in tissues, gut contents, diet items, and water at site of capture, of adult beavers from the Serpent River drainage basin which contains U tailings at Elliot Lake, Ontario, and from nearby control sites. Levels of (226)Ra in beaver bone, muscle and kidney were highest in animals from locations close to U tailings; liver levels did not vary by site. Environmental (226)Ra levels were within ranges previously reported at these or similar locations elsewhere; levels in beaver gut contents reflected levels in diet items. Concentration ratios exceeded unity only between some vegetation items and beaver bone at the Elliot Lake site and were less than 0.19 between vegetation and other tissues. In two beavers with tissue levels of (226)Ra higher than other sampled, neither (232)Th nor (230)Th were detected in bone, muscle or liver tissues. U-238 was measurable in bone, muscle and liver, (228)Th in bone, (210)Po bone, muscle and liver; and (210)Pb was measurable only in bone. Estimated yearly intakes of radionuclides by people eating beavers were calculated to be below current allowable levels set by the Canadian regulatory authorities.

  13. STUDY OF NATURAL RADIOACTIVITY (226Ra, 232Th AND 40K) IN SOIL SAMPLES FOR THE ASSESSMENT OF AVERAGE EFFECTIVE DOSE AND RADIATION HAZARDS.

    PubMed

    Bangotra, Pargin; Mehra, Rohit; Kaur, Kirandeep; Jakhu, Rajan

    2016-10-01

    The activity concentration of (226)Ra (radium), (232)Th (thorium) and (40)K (potassium) has been measured in the soil samples collected from Mansa and Muktsar districts of Punjab (India) using NaI (Tikl) gamma detector. The concentration of three radionuclides ((226)Ra, (232)Th and (40)K) in the studied area has been varied from 18±4 to 46±5, 53±7 to 98±8 and 248±54 to 756±110 Bq kg(-1), respectively. Radium equivalent activities (Raeq) have been calculated in soil samples for the assessment of the radiation hazards arising due to the use of these soil samples. The absorbed dose rate of (226)Ra, (232)Th and (40)K in studied area has been varied from 8 to 21, 33 to 61 and 9 to 25 nGy h(-1), respectively. The corresponding indoor and outdoor annual effective dose in studied area was 0.38 and 0.09 mSv, respectively. The external and internal hazard has been also calculated for the assessment of radiation hazards in the studied area.

  14. Activity concentration, transfer factors and resultant radiological risk of 226Ra, 232Th, and 40K in soil and some vegetables consumed in Selangor, Malaysia

    NASA Astrophysics Data System (ADS)

    Solehah, A. R.; Yasir, M. S.; Samat, S. B.

    2016-11-01

    The activity concentrations of the natural radionuclides 226Ra, 232Th, and 40K were determined in vegetable crops consumed by Malaysian people in Sungai Besar, Selangor. Sample of vegetables and the soil where the crops were cultivated and collected at five different location. The activity concentrations in Bq/kg of 226Ra, 232Th, and 40K were measured by the gamma-ray spectroscopy using the high purity germanium detector. The range activity concentration in soil is between 51.81 and 71.84 Bq/kg, 64.18 and 78.00 Bq/kg, and 210.49 and 244.29 Bq/kg for 226Ra, 232Th, and 40K, respectively. The activity concentration of 226Ra, 232Th, and 40K in vegetables were found to be in the range of 2.06 to 5.44 Bq/kg, Not Detectable to 0.61 Bq/kg, and 101.00 to 1223.09 Bq/kg, respectively. The activity concentration in both soil and vegetables were all less than lower limit stated by UNSCEAR. The Transfer Factors range value for 226Ra, 232Th, and 40K varied from 0.02 to 0.06, 0.003 to 0.008, and 1.79 to 5.19 respectively. Radium equivalent for soil range from 165.57 to 194.84 Bq/kg. It was within the international accepted value (370 Bq/kg). Absorb dose rate for soil range between 73.5 to 86.40 nGyh-1, in safe range from limit of international accepted value (55nGyh-1). Effective dose rate is found to be in range of 0.09 to 0.11 mSvy-1 for soil which is less than 2.4 mSv/y. External and Internal Hazard indices of soil was all below 1, within agreement of other researcher and UNSCEAR. The estimation of the consequent radiological risk due to the presence of those radionuclides is significantly low.

  15. Determination of (210)Pb and (226)Ra/(228)Ra in continental water using HIDEX 300SL LS-spectrometer with TDCR efficiency tracing and optimized α/β-discrimination.

    PubMed

    Eikenberg, J; Beer, H; Jäggi, M

    2014-11-01

    An analytical method for determination of (210)Pb, (226)Ra and (228)Ra is presented based on adsorption on 3M Empore RadDiscs, and measurement applying liquid scintillation spectrometry (LSC) after elution. The LSC measurement was performed with optimized α/β-discrimination and isotope standardization using the triple to double coincidence ratio (TDCR). The consistency of measurement results between radioactive parent-daughter pairs (210)Pb/(210)Bi, (226)Ra/(222)Rn and (228)Ra/(228)Ac was checked in long-term counting experiments and the influence ofinterference of in-growing daughters from (226)Ra into the β-spectrum of (228)Ra+(228)Ac was studied as well. Recommendations for optimized LSC (228)Ra measurement besides presence of (226)Ra are given.

  16. The Application of 238U/235U as a Redox-Proxy for Past Ocean Chemistry

    NASA Astrophysics Data System (ADS)

    Andersen, M. B.; Westermann, S.; Bahniuk, A.; Vasconcelos, C.; McKenzie, J. A.; Föllmi, K. B.; Vance, D.

    2014-12-01

    The recent discovery of significant variation in 238U/235U caused by redox change at the surface Earth has led to its use to extract information on the oxygenation state of ancient oceans from marine sediments [e.g. 1]. Recent studies have focused on improving the understanding of the 238U/235U signature in modern marine carbonates [2] and black shales [3] to improve the robustness of this tracer. To further advance its use we have focused on improving our understanding of 238U/235U systematics in modern dolomite, another commonly occurring rock-type in the geological record, before turning to 238U/235U signatures in ancient sediments. The measured dolomite samples, precipitated in modern environments of coastal hypersaline lagoons in Brazil, all exhibit 238U/235U values that deviate from the seawater composition [3]. Observed values are both lighter (ca. 130 ppm; as also observed in dolomite from tidal-ponds on Bahamas [2]) and heavier (50-180 ppm). These distinct 238U/235U values for different dolomite-precipitates likely attest to the particular formation style, as well as early diagenetic processes. We use such modern settings to discuss the utility of 238U/235U in ancient sediments, the singularity of any observed 238U/235U signal, its relation to global ocean chemistry and potential diagenetic overprinting. These constraints are then used to evaluate a well-preserved marine carbonate section [4] and published black shale 238U/235U data [1], both deposited during the Oceanic Anoxic Event 2 (93 Ma). We discuss the capabilities of both the carbonate and black shale section for retaining information on the 238U/235U composition in the ocean during OAE 2. [1] Montoya-Pino et al. (2010) Geology, 38, 315-318 [2] Romaniello et al. (2013) 362, 305-316 [3] Andersen et al. (2014) EPSL, 400, 184-194 [4] Westermann et al. (2010) Cret. Res., 31, 500-514

  17. Concentration of natural radionuclides in raw water and packaged drinking water and the effect of water treatment.

    PubMed

    Manu, Anitha; Santhanakrishnan, V; Rajaram, S; Ravi, P M

    2014-12-01

    The raw water (RW) samples collected from natural sources are subjected to water treatment process, including reverse osmosis (RO), and are packed in bottles as packaged drinking water (PDW). Raw water (21 samples) taken from deep wells of Chennai and Secunderabad which are used in the production of PDW, were analysed for (234)U, (235)U, (238)U, (226)Ra, (228)Ra and (210)Pb activity concentrations. Activity Concentrations of (234)U, (235)U, (238)U, (226)Ra, (228)Ra, (210)Pb and (210)Po in PDW were also analysed. The mean activity concentrations of (234)U, (235)U, (238)U, (226)Ra, (228)Ra and (210)Pb in RW at Chennai were 12.1, ≤1.3, 7.1, 2.6, 27.5, and 16.3 mBq/L respectively. The mean activity concentrations of (234)U, (235)U, (238)U, (226)Ra, (228)Ra and (210)Pb in RW at Secunderabad were found to be 40.9, 1.7, 41.5 84.5, 100.1, and 17.0 mBq/L respectively. The mean concentrations of (234)U, (235)U, (238)U, (226)Ra, (228)Ra, (210)Pb and (210)Po in PDW at Chennai were found to be ≤1.3, ≤1.3, ≤1.3, ≤0.2, ≤1.7, 28.0 and 1.2 mBq/L at Secunderabad were found to be ≤1.3, ≤1.3, 1.7, 4.3, 5.0 and 28.1 mBq/L. The study indicated a considerable reduction in the concentration of natural radionuclides due to water treatment. The reduction ratios of RW to PDW for (234)U, (238)U, (226)Ra, (228)Ra were 97, 96, 94 and 95%. In case of (210)Pb, the PDW showed higher concentration of (210)Pb than RW. This was due to its in growth from (222)Rn which was not removed in the RO process.

  18. Determination of gross alpha, 224Ra, 226Ra, and 228Ra activities in drinking water using a single sample preparation procedure.

    PubMed

    Parsa, Bahman; Obed, Reynaldo N; Nemeth, William K; Suozzo, Gail P

    2005-12-01

    The current federal and New Jersey State regulations have greatly increased the number of gross alpha and radium tests for public and private drinking water supplies. The determination of radium isotopes in water generally involves lengthy and complicated processes. In this study, a new approach is presented for the determination of gross alpha, 224Ra, 226Ra, and 228Ra activities in water samples. The method includes a single sample preparation procedure followed by alpha counting and gamma-ray spectroscopy. The sample preparation technique incorporates an EPA-approved co-precipitation methodology for gross alpha determination with a few alterations and improvements. Using 3-L aliquots of sample, spiked with 133Ba tracer, the alpha-emitting radionuclides are isolated by a BaSO4 and Fe(OH)3 co-precipitation scheme. First the gross alpha-particle activity of the sample is measured with a low-background gas-flow proportional counter, followed by radium isotopes assay by gamma-ray spectroscopy, using the same prepared sample. Gamma-ray determination of 133Ba tracer is used to assess the radium chemical recovery. The 224Ra, 226Ra, and 228Ra activities in the sample are measured through their gamma-ray-emitting decay products, 212Pb, 214Pb/214Bi, and 228Ac, respectively. In cases where 224Ra determination is required, the gamma-ray counting should be performed within 2-4 d from sample collection. To measure 226Ra activity in the sample, the gamma-ray spectroscopy can be repeated 21 d after sample preparation to ensure that 226Ra and its progeny have reached the equilibrium state. At this point, the 228Ac equilibration with parent 228Ra is already established. Analysis of aliquots of de-ionized water spiked with NIST-traceable 230Th, 224Ra, 226Ra, and 228Ra standards demonstrated the accuracy and precision of this method. Various performance evaluation samples were also assayed for gross alpha as well as radium isotope activity determination using this procedure and the

  19. 210Pb-226Ra chronology reveals rapid growth rate of Madrepora oculata and Lophelia pertusa on world's largest cold-water coral reef

    NASA Astrophysics Data System (ADS)

    Sabatier, P.; Reyss, J.-L.; Hall-Spencer, J. M.; Colin, C.; Frank, N.; Tisnérat-Laborde, N.; Bordier, L.; Douville, E.

    2011-12-01

    Here we show the use of the 210Pb-226Ra excess method to determine the growth rate of corals from one of the world's largest known cold-water coral reef, the Røst Reef off Norway. Two large branching framework-forming cold-water coral specimens, one Lophelia pertusa and one Madrepora oculata were collected alive at 350 m water depth from the Røst Reef at ~67° N and ~9° E. Pb and Ra isotopes were measured along the major growth axis of both specimens using low level alpha and gamma spectrometry and the corals trace element compositions were studied using ICP-QMS. Due to the different chemical behaviors of Pb and Ra in the marine environment, 210Pb and 226Ra were not incorporated the same way into the aragonite skeleton of those two cold-water corals. Thus to assess of the growth rates of both specimens we have here taken in consideration the exponential decrease of initially incorporated 210Pb as well as the ingrowth of 210Pb from the decay of 226Ra. Moreover a~post-depositional 210Pb incorporation is found in relation to the Mn-Fe coatings that could not be entirely removed from the oldest parts of the skeletons. The 226Ra activities in both corals were fairly constant, then assuming constant uptake of 210Pb through time the 210Pb-226Ra chronology can be applied to calculate linear growth rate. The 45.5 cm long branch of M. oculata reveals an age of 31 yr and a~linear growth rate of 14.4 ± 1.1 mm yr-1, i.e. 2.6 polyps per year. However, a correction regarding a remaining post-depositional Mn-Fe oxide coating is needed for the base of the specimen. The corrected age tend to confirm the radiocarbon derived basal age of 40 yr (using 14C bomb peak) with a mean growth rate of 2 polyps yr-1. This rate is similar to the one obtained in Aquaria experiments under optimal growth conditions. For the 80 cm-long specimen of L. pertusa a remaining contamination of metal-oxides is observed for the middle and basal part of the coral skeleton, inhibiting similar accurate age

  20. Transmission Nuclear Resonance Fluorescence Measurements of 238U in Thick Targets

    SciTech Connect

    Quiter, Brian J.; Ludewigt, Bernhard A.; Mozin, Vladimir V.; Wilson, Cody; Korbly, Steve

    2010-08-31

    Transmission nuclear resonance fluorescence measurements were made on targets consisting of Pb and depleted U with total areal densities near 86 g/cm2. The 238U content n the targets varied from 0 to 8.5percent (atom fraction). The experiment demonstrates the capability of using transmission measurements as a non-destructive technique to identify and quantify the presence of an isotope in samples with thicknesses comparable to he average thickness of a nuclear fuel assembly. The experimental data also appear to demonstrate the process of notch refilling with a predictable intensity. Comparison of measured spectra to previous backscatter 238U measurements indicates general agreement in observed excited states. Two new 238U excited states and possibly a third state have also been observed.

  1. Photofission of {sup 238}U in the giant-resonance region

    SciTech Connect

    Dzhilavyan, L. Z. Nedorezov, V. G.

    2013-12-15

    Data on cross sections for the reaction {sup 238}U(γ,F) in the giant-resonance region were analyzed in connection with the preparation of new experiments aimed at studying {sup 238}U photofission—in particular, in beams of photons from in-flight positron annihilation on internal targets of positron storage rings. These data were taken from measurements also performed with annihilation photons but from positron beams external to the accelerators used. The procedures applied in such measurements and based both on processing the multiplicity of detected neutrons and on detecting fission fragments were also analyzed.

  2. Assessment of environmental (226)Ra, (232)Th and (40)K concentrations in the region of elevated radiation background in Segamat District, Johor, Malaysia.

    PubMed

    Saleh, Muneer Aziz; Ramli, Ahmad Termizi; Alajerami, Yasser; Aliyu, Abubakar Sadiq

    2013-10-01

    Extensive environmental survey and measurements of gamma radioactivity in the soil samples collected from Segamat District were conducted. Two gamma detectors were used for the measurements of background radiation in the area and the results were used in the computation of the mean external radiation dose rate and mean weighted dose rate, which are 276 nGy h(-1) and 1.169 mSv y(-1), respectively. A high purity germanium (HPGe) detector was used in the assessment of activity concentrations of (232)Th, (226)Ra and (40)K. The results of the gamma spectrometry range from 11 ± 1 to 1210 ± 41 Bq kg(-1) for (232)Th, 12 ± 1 to 968 ± 27 Bq kg(-1) for (226)Ra, and 12 ± 2 to 2450 ± 86 Bq kg(-1) for (40)K. Gross alpha and gross beta activity concentrations range from 170 ± 50 to 4360 ± 170 Bq kg(-1) and 70 ± 20 to 4690 ± 90 Bq kg(-1), respectively. These results were used in the plotting of digital maps (using ARCGIS 9.3) for isodose. The results are compared with values giving in UNSCEAR 2000.

  3. Round-robin 230Th–234U age dating of bulk uranium for nuclear forensics

    DOE PAGES

    Gaffney, Amy M.; Hubert, Amélie; Kinman, William S.; ...

    2015-07-30

    In an inter-laboratory measurement comparison study, four laboratories determined 230Th–234U model ages of uranium certified reference material NBL U050 using isotope dilution mass spectrometry. The model dates determined by the participating laboratories range from 9 March 1956 to 19 October 1957, and are indistinguishable given the associated measurement uncertainties. As a result, these model ages are concordant with to slightly older than the known production age of NBL U050.

  4. Production of neutron-rich transcalifornium nuclei in 238U-induced transfer reactions

    NASA Astrophysics Data System (ADS)

    Zhu, Long; Su, Jun; Xie, Wen-Jie; Zhang, Feng-Shou

    2016-11-01

    In order to produce more unknown neutron-rich transcalifornium nuclei, the collisions of 238U with the targets 248Cm, 249Cf, and 250Cm are investigated within the framework of the dinuclear system model. The production cross sections of unknown neutron-rich nuclei with Z =99 -104 in these reactions are predicted. The influences of N /Z ratios and charge numbers of the targets on the production cross sections are studied. It is found that high N /Z ratios of 248Cm and 250Cm targets enhance the production cross sections of neutron-rich transcalifornium nuclei. However, due to high charge number of the target 249Cf the predicted production cross sections of unknown neutron-rich nuclei with Z =104 in the reaction 238U+249Cf are higher than those in 238U+248Cm . We also have studied the entrance angular momentum effects on production probabilities of transfer products in the reaction 238U+248Cm . It is found that the formation probabilities of the final neutron-rich products increase first and then decrease with the increasing J .

  5. Measurements of (234)U and (238)U in hair, urine, and drinking water among drilled bedrock well water users for the evaluation of hair as a biomonitor of uranium intake.

    PubMed

    Israelsson, Axel; Pettersson, Håkan

    2014-08-01

    Hair is evaluated and compared with urine as a biomonitor for human intake of uranium. Concentrations of U and U and the activity ratio between them are measured in the hair, urine, and drinking water of 24 drilled bedrock well water users in Östergötland, Sweden. The samples are measured with α-spectrometry after radiochemical preparation using liquid-liquid separation with tributylphosphate. The results show that there is a stronger correlation between the uranium concentrations in the drinking water of each subject and the hair of the subject (r = 0.50) than with the urine (r = 0.21). There is also a stronger correlation between the activity ratios of water and hair (r = 0.91) than between water and urine (r = 0.56). These results imply that hair may serve as a robust indicator of chronic uranium intake. One obvious advantage over sampling urine is that hair samples reflect a much longer excretion period: weeks compared to days. The absorbed fraction of uranium, the f value, is calculated as the ratio between the excreted amount of uranium in urine and hair per day and the daily drinking water intake of uranium. The f values stretch from 0.002 to 0.10 with a median of 0.023.

  6. Concurrent determination of 224Ra, 226Ra, 228Ra, and unsupported 212Pb in a single analysis for drinking water and wastewater: dissolved and suspended fractions.

    PubMed

    Parsa, Bahman; Obed, Reynaldo N; Nemeth, William K; Suozzo, Gail

    2004-02-01

    A technique has been developed for the measurement of 224Ra, 226Ra, 228Ra, and unsupported 2t2Pb concurrently in a single analysis. The procedure can be applied to both drinking water and wastewater, including the dissolved and suspended fractions of a sample. For drinking water samples, using 3-L aliquots, the radium isotopes are isolated by a fast PbSO4 co-precipitation and then quantified by gamma-ray spectroscopy. The radium isotopes 224Ra, 226Ra, and 228Ra are measured through their gamma-ray-emitting decay products, 212Pb, 214Pb (and/or 214Bi), and 228Ac, respectively. Because of the short half-life of 224Ra (T1/2 = 3.66 d), the precipitate should be counted within 4 d of the sample collection date. In case the measurement of unsupported 212Pb (T1/2 = 10.64 h) is required, the gamma-ray analysis should be initiated as soon as possible, preferably on the same day of collection. The counting is repeated after about 21 d to ensure the 226Ra progeny are in equilibrium with their parent. At this point, the 228Ac equilibration with its 228Ra parent is already established. In the case of samples containing suspended materials, an aliquot of sample is filtered and then the filtrate is treated as described above for drinking water samples. The suspended fraction of sample, collected on the filter, is directly analyzed by gamma-ray spectroscopy with no further chemical separation. Aliquots of de-ionized water spiked with various radium standards were analyzed to check the accuracy and precision of the method. In addition, analysis results of actual samples using this method were compared with the ones performed using U.S. Environmental Protection Agency-approved procedures, and the measured values were in close agreement. This method simplifies the analytical procedures and reduces the labor while achieving the precision, accuracy, and minimum detection concentration requirements of EPA's Regulations.

  7. Measurement of activity concentrations of 40K, 226Ra and 232Th for assessment of radiation hazards from soils of the southwestern region of Nigeria.

    PubMed

    Ajayi, Oladele Samuel

    2009-08-01

    Activity concentrations of the selected radionuclides (40)K, (226)Ra and (232)Th were measured in surface soil samples collected from 38 cities in the southwest region of Nigeria by means of gamma spectroscopy with a high-purity germanium detector. Measured activity concentration values of (40)K varied from 34.9 +/- 4.4 to 1,358.6 +/- 28.5 Bq kg(-1) (given on a dry mass (DM) basis) with a mean value of 286.5 +/- 308.5 Bq kg(-1); that of (226)Ra varied from 9.3 +/- 3.7 to 198.1 +/- 13.8 Bq kg(-1) with a mean value of 54.5 Bq kg(-1) and a standard deviation of 38.7 Bq kg(-1), while that of (232)Th varied from 5.4 +/- 1.1 to 502.0 +/- 16.5 Bq kg(-1) with a mean value of 91.1 Bq kg(-1) and standard deviation of 100.9 Bq kg(-1). The mean activity concentration values obtained for (226)Ra and (232)Th are greater than the world average values reported by the United Nations Scientific Committee on Effects of Atomic Radiation for areas of normal background radiation. Radiological indices were estimated for the radiation/health hazards of the natural radioactivity of all soil samples. Estimated absorbed dose rates in air varied from 12.42 +/- 2.25 to 451.33 +/- 19.06 nGy h(-1), annual outdoor effective dose rates from 0.015 +/- 0.003 to 0.554 +/- 0.023 mSv year(-1), internal hazard index from 0.10 +/- 0.03 to 3.02 +/- 0.16, external hazard index from 0.07 +/- 0.01 to 2.60 +/- 0.11, representative level index from 0.19 +/- 0.03 to 6.84 +/- 0.29, activity index from 0.09 +/- 0.02 to 3.42 +/- 0.15, and radium equivalent activity from 26.95 +/- 5.04 to 963.15 +/- 41.87 Bq kg(-1). Only the mean value of the representative level index exceeds the limit for areas of normal background radiation. All other indices show mean values that are lower than the recommended limits.

  8. Fractionation of natural radionuclides in soils from the vicinity of a former uranium mine Zirovski vrh, Slovenia.

    PubMed

    Strok, Marko; Smodis, Borut

    2010-01-01

    As a result of former uranium mining and milling activities at Zirovski vrh, Slovenia, 0.6 million tons of uranium mill tailings (UMT) were deposited onto a nearby waste pile Borst. Resulting enhanced levels of natural radionuclides in UMT could pose threat for the surrounding environment. Therefore, sequential extraction protocol was performed to assess mobility and bioavailability of (238)U, (234)U, (230)Th and (226)Ra in soils from the waste pile and its surrounding. The radionuclides associated with exchangeable, organic, carbonate, Fe/Mn oxides and residual fraction, respectively, were determined. Results showed that the highest activity concentrations for the studied radionuclides were on the bottom of the waste pile. In non-contaminated locations, about 80% of all radionuclides were in the residual fraction. Considering activity concentrations in the UMT, (238)U and (234)U are the most mobile. Mobility of (226)Ra is suppressed by high sulphate concentrations and is similar to mobility of (230)Th.

  9. Dissolved uranium, radium and radon evolution in the Continental Intercalaire aquifer, Algeria and Tunisia.

    PubMed

    Elliot, Trevor; Bonotto, Daniel Marcos; Andrews, John Napier

    2014-11-01

    Natural, dissolved (238)U-series radionuclides (U, (226)Ra, (222)Rn) and activity ratios (A.R.s: (234)U/(238)U; (228)Ra/(226)Ra) in Continental Intercalaire (CI) groundwaters and limited samples from the overlying Complexe Terminal (CT) aquifers of Algeria and Tunisia are discussed alongside core measurements for U/Th (and K) in the contexts of radiological water quality, geochemical controls in the aquifer, and water residence times. A redox barrier is characterised downgradient in the Algerian CI for which a trend of increasing (234)U/(238)U A.R.s with decreasing U-contents due to recoil-dominated (234)U solution under reducing conditions allows residence time modelling ∼500 ka for the highest enhanced A.R. = 3.17. Geochemical modelling therefore identifies waters towards the centre of the Grand Erg Oriental basin as palaeowaters in line with reported (14)C and (36)Cl ages. A similar (234)U/(238)U trend is evidenced in a few of the Tunisian CI waters. The paleoage status of these waters is affirmed by both noble gas recharge temperatures and simple modelling of dissolved, radiogenic (4)He-contents both for sampled Algerian and Tunisian CI and CT waters. For the regions studied these waters therefore should be regarded as "fossil" waters and treated effectively as a non-renewable resource.

  10. Short and long term bystander effect induction by fathead minnows (Pimephales promelas, Rafinesque, 1820) injected with environmentally relevant whole body doses of 226Ra.

    PubMed

    Smith, Richard W; Seymour, Colin B; Mothersill, Carmel E

    2013-12-01

    Bystander effect induction by fathead minnows injected with environmentally relevant doses of (226)Ra was investigated. Twenty four h and 6 months after injection with a single dose of 21, 210 or 2100 μBq, fin tissue samples emitted a pro-apoptotic signal, which reduced the clonogenic survival of an apoptosis sensitive reporter cell line. Twenty four h and 10 weeks after injection explants from non-injected bystander fish, swum with the injected fish, also emitted a pro-apoptotic signal. However 6 months after injection the bystander fish to 21 and 210 μBq injected fish emitted an anti-apoptotic signal. This demonstrates that extremely low dose irradiation can have effects outside of the irradiated fish. This has implications for population and ecosystem responses to contamination.

  11. Distribution and possible dietary intake of radioactive 137Cs, 40K and 226Ra with the pantropical mushroom Macrocybe gigantea in SW China.

    PubMed

    Falandysz, Jerzy; Zhang, Ji; Zalewska, Tamara; Apanel, Anna; Wang, Yuanzhong; Wiejak, Anna

    2015-01-01

    There is scarcity of data on contamination with radiocesium 134/137Cs of edible mushrooms from the Southwestern Asia. This study aimed to get insight into activity concentration of artificial nuclides 134/137Cs and natural 40K and 226Ra in mushrooms from Yunnan province, which is major producer in China. The specimens of pantropical mushroom Macrocybe gigantea were collected from the wild and from a farm across Yunnan land in 2012-2013 and analyzed using gamma spectrometry with hyperpure germanium coaxial detector (HPGe). M. gigantea showed low activity concentrations of 137Cs (median value for dehydrated caps was 4.5 Bq kg(-1) and 5.4 Bq kg(-1) for stipes) while 134Cs was not detected. Natural radionuclide 40K showed 2-3 orders of magnitude greater activity concentration compared to artificial 137Cs in M. gigantea. The activity concentrations of 226Ra from uranium and radium decay series for most of the consignments of M. gigantea examined were below the method's limit of detection. The nominal effective dose equivalent for the Yunnan people from the dietary intake of 137Cs was assessed to be below 0.01 μSv per annum on the average, and that from 40K to be below 0.1 μSv per annum. Data available for the first time on activity concentrations of 137Cs in wild-grown saprobic mushroom from this region of Asia suggest low pollution with radiocesium from fallout there. Hence, the likely health risks from intake of 137Cs from cooked M. gigantea are in practice of mushrooms absent for human consumers there. Because of abundance of mushrooms in Yunnan and high significance of the region as producer and exporter a wider study using many species is necessary to fill a gap on possible radioactive contamination and risk to mushroom consumers.

  12. 238U, and its decay products, in grasses from an abandoned uranium mine

    NASA Astrophysics Data System (ADS)

    Childs, Edgar; Maskall, John; Millward, Geoffrey

    2016-04-01

    Bioaccumulation of radioactive contaminants by plants is of concern particularly where the sward is an essential part of the diet of ruminants. The abandoned South Terras uranium mine, south west England, had primary deposits of uraninite (UO2) and pitchblende (U3O8), which contained up to 30% uranium. When the mine was active uranium and radium were extracted but following closure it was abandoned without remediation. Waste rock and gangue, consisting of inefficiently processed minerals, were spread around the site, including a field where ruminants are grazed. Here we report the activity concentrations of 238U, 235U 214,210Pb, and the concentrations of selected metals in the soils, roots and leaves of grasses taken from the contaminated field. Soil samples were collected at the surface, and at 30 cm depth, using an auger along a 10-point transect in the field from the foot of a waste heap. Whole, individual grass plants were removed with a spade, ensuring that their roots were intact. The soils and roots and grass leaves were freeze-dried. Activity concentrations of the radionuclides were determined by gamma spectroscopy, following 30 days incubation for development of secular equilibrium. Dried soils, roots and grasses were also digested in aqua regia and the concentrations of elements determined by ICP techniques. Maximum activity concentrations of 238U, 235U, 214Pb and 210Pb surface soils were 63,300, 4,510, 23,300 and 49,400 Bq kg-1, respectively. The mean 238U:235U ratio was 11.8 ± 1.8, an order of magnitude lower than the natural value of 138, indicating disequilibrium within the decay chain due to mineral processing. Radionuclides in the roots had 5 times lower concentration and only grass leaves in the vicinity of the waste heap had measureable values. The mean soil to root transfer factor for 238U was 36%, the mean root to leaf was 3% and overall only 0.7% of 238U was transferred from the soil to the leaves. The roots contained 0.8% iron, possibly as

  13. Study of 234U(n,f) Resonances Measured at the CERN n_TOF Facility

    NASA Astrophysics Data System (ADS)

    Leal-Cidoncha, E.; Durán, I.; Paradela, C.; Tarrío, D.; Leong, L. S.; Audouin, L.; Tassan-Got, L.; Praena, J.; Berthier, B.; Ferrant, L.; Isaev, S.; Le Naour, C.; Stephan, C.; Trubert, D.; Abbondanno, U.; Aerts, G.; Álvarez, H.; Álvarez-Velarde, F.; Andriamonje, S.; Andrzejewski, J.; Badurek, G.; Baumann, P.; Bečvář, F.; Berthoumieux, E.; Calviño, F.; Calviani, M.; Cano-Ott, D.; Capote, R.; Carrapiço, C.; Cennini, P.; Chepel, V.; Chiaveri, E.; Colonna, N.; Cortes, G.; Couture, A.; Cox, J.; Dahlfors, M.; David, S.; Dillmann, I.; Domingo-Pardo, C.; Dridi, W.; Eleftheriadis, C.; Embid-Segura, M.; Ferrari, A.; Ferreira-Marques, R.; Fujii, K.; Furman, W.; Gonçalves, I.; González-Romero, E.; Gramegna, F.; Guerrero, C.; Gunsing, F.; Haas, B.; Haight, R.; Heil, M.; Herrera-Martinez, A.; Igashira, M.; Jericha, E.; Kadi, Y.; Käppeler, F.; Karadimos, D.; Kerveno, M.; Koehler, P.; Kossionides, E.; Krtička, M.; Lampoudis, C.; Leeb, H.; Lindote, A.; Lopes, I.; Lozano, M.; Lukic, S.; Marganiec, J.; Marrone, S.; Martínez, T.; Massimi, C.; Mastinu, P.; Mengoni, A.; Milazzo, P. M.; Moreau, C.; Mosconi, M.; Neves, F.; Oberhummer, H.; O'Brien, S.; Oshima, M.; Pancin, J.; Papadopoulos, C.; Pavlik, A.; Pavlopoulos, P.; Perrot, L.; Pigni, M. T.; Plag, R.; Plompen, A.; Plukis, A.; Poch, A.; Pretel, C.; Quesada, J.; Rauscher, T.; Reifarth, R.; Rubbia, C.; Rudolf, G.; Rullhusen, P.; Salgado, J.; Santos, C.; Sarchiapone, L.; Savvidis, I.; Tagliente, G.; Tain, J. L.; Tavora, L.; Terlizzi, R.; Vannini, G.; Vaz, P.; Ventura, A.; Villamarin, D.; Vincente, M. C.; Vlachoudis, V.; Vlastou, R.; Voss, F.; Walter, S.; Wiescher, M.; Wisshak, K.

    2014-05-01

    We present the analysis of the resolved resonance region for the 234U(n,f) cross section data measured at the CERN n_TOF facility. The resonance parameters in the energy range from 1 eV to 1500 eV have been obtained with the SAMMY code by using as initial parameters for the fit the resonance parameters of the JENDL-3.3 evaluation. In addition, the statistical analysis has been accomplished, partly with the SAMDIST code, in order to study the level spacing and the Mehta-Dyson correlation.

  14. Natural Variation of 238U/235U in Geo- and Cosmochemistry

    NASA Astrophysics Data System (ADS)

    Weyer, S.; Brennecka, G.; Montoya Pino, C.; Noordmann, J.; Schauble, E. A.; Wadhwa, M.; Anbar, A. D.

    2009-12-01

    The ratio of the two primordial U isotopes has long been assumed to be invariant (i.e. 238U/235U = 137.88, [1]) in the Solar [1, 2]. Due to analytical improvements, small (‰-range) U isotope variations can now be detected in both terrestrial [3, 4, 5] and meteoritic materials [6]. Uranium isotope variations on Earth are produced by chemical reactions, analogous to stable isotope fractionation, although U has no stable isotopes. The range of U isotope variations observed thus far on Earth exceeds 1‰ and is mostly driven by nuclear field shift effects, which depend on nuclear volume rather than mass [7]. The strongest isotope fractionation appears to occur between oxidized and reduced U species (UVI and UIV). As a result, oxic environments (e.g., seawater) are enriched in the light U isotope, 235U, while anoxic sediments (e.g., from the Black Sea) are enriched in the heavy U isotope, 238U [4]. This redox-sensitive behavior of U isotope compositions makes the 238U/235U ratio promising for use as a paleo-redox proxy. In paleoceanography, 238U/235U ratios can be used to estimate the extent of seafloor anoxia. During periods of enhanced global ocean anoxia (e.g., during the mid-Cretaceous oceanic anoxic event OAE-2) heavy U was preferentially buried into anoxic sediments. Accordingly, sea water and all oceanic sinks became depleted in heavy U. We used this shift in U isotope compositions to estimate a three times enhancement of anoxic environments in the oceans during OAE-2 compared to today [8]. In meteoritic materials, 238U/235U variations may be produced by (1) chemical reactions (2) nucleosynthetic anomalies and/or (3) decay of the short-lived extant 247Cm (half life = 15.6 Ma) to 235U. We investigated the U isotope composition of calcium aluminum-rich inclusions (CAIs). The Pb-Pb ages of CAIs define the age of the Solar System, as they represent the first solids to condense from the cooling protoplanetary disk. The investigated CAIs from the Allende meteorite

  15. Evidence of complete fusion in the subbarrier {sup 16}O+{sup 238}U reaction

    SciTech Connect

    Nishio, K. Ikezoe, H.; Asai, M.; Tsukada, K.; Mitsuoka, S.; Tsuruta, K.; Satou, K.; Lin, C. J.; Ohsawa, T.

    2006-08-15

    Evaporation residue cross sections in the {sup 16}O+{sup 238}U reaction were measured for the energy range from above-to extreme subbarrier. We used a He-gas-jet system to transport the fusion products, and the {alpha} decay of the evaporation residues was measured by using a rotating wheel system. The measured cross sections for {sup 248,249,250}Fm are reproduced by a statistical model calculation, for which partial cross sections are calculated by a coupled-channel model taking into account the prolate deformation of {sup 238}U. We conclude that complete fusion is the main process in the subbarrier energy region, and quasifission is not an important channel.

  16. Determination of 235U/238U Ratio on Urine by ICP-MS

    SciTech Connect

    Collins, L; Gobaleza, A; Langston, R; Radev, R; Than, C; Wong, C; Wood-Zika, A

    2011-10-19

    LLNL Internal Dosimetry Program - The new procedure satisfies the requirement to determine {sup 235}U/{sup 238}U ratio in bioassay urine samples. MDA - The L{sub C} and MDA{sub 95} for {sup 235}U are well below the required detection limit of 0.00035 {mu}g/L. Turn around time - Analysis of 10 samples plus 2 QCs can be completed in one work day (8 hours).

  17. /sup 230/Th - /sup 238/U disequilibrium systematics in young volcanic rocks

    SciTech Connect

    Newman, S.

    1983-01-01

    Radioactive disequilibrium between /sup 230/Th (t/sub .5/ = 75,200 years) and its parent, /sup 238/U, has two major applications to the study of young volcanic rocks: 1) geochronology and 2) geochemical tracer studies. Geochronological investigations include both the dating of young (< approx.250,000 year-old) lavas by the internal isochron method and the study of the temporal evolution of magma systems feeding volcanoes. Older, K-Ar-dated lavas from Mauna Kea, Hawaii and Marion Island (Prince Edward hot spot) exhibit constant initial (/sup 230/Th//sup 232/Th) (activity) ratios for the past 100,000-275,000 years. At Mt. Shasta, California, a general decrease in (/sup 230/Th//sup 232/Th)/sub 0/ through time, with evidence of possible mixing corroborated by other geochemical data, is observed. Geochemical tracer studies depend on the observations that Th/U and (/sup 230/Th//sup 238/U) can be changed by such processes as partial melting, mixing, or fluid transport, whereas (/sup 230/Th//sup 232/Th) can only be modified by mixing or the passage of time. The (/sup 230/Th//sup 238/U) ratio can be used to identify possible petrogenetic processes. All lavas exhibit (/sup 230/Th//sup 238/U) greater than or equal to 1 except for some from the Aleutians and Marianas. These observations suggest that subduction-related volcanism is the only type in which U may behave as a more incompatible element than Th, although it need not (Cascades). Recent vapor transport of U or retention of Th may explain the U-enrichment in island arc lavas.

  18. Solubility of 238U radionuclide from various types of soil in synthetic gastrointestinal fluids using "US in vitro" digestion method

    NASA Astrophysics Data System (ADS)

    Rashid, Nur Shahidah Abdul; Sarmani, Sukiman; Majid, Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok

    2015-04-01

    238U radionuclide is a naturally occuring radioactive material that can be found in soil. In this study, the solubility of 238U radionuclide obtained from various types of soil in synthetic gastrointestinal fluids was analysed by "US P in vitro" digestion method. The synthetic gastrointestinal fluids were added to the samples with well-ordered, mixed throughly and incubated according to the human physiology digestive system. The concentration of 238U radionuclide in the solutions extracted from the soil was measured using Induced Coupling Plasma Mass Spectrometer (ICP-MS). The concentration of 238U radionuclide from the soil samples in synthetic gastrointestinal fluids showed different values due to different homogenity of soil types and chemical reaction of 238U radionuclide. In general, the solubility of 238U radionuclide in gastric fluid was higher (0.050 - 0.209 ppm) than gastrointestinal fluids (0.024 - 0.050 ppm). It could be concluded that the US P in vitro digestion method is practicle for estimating the solubility of 238U radionuclide from soil materials and could be useful for monitoring and risk assessment purposes applying to environmental, health and contaminated soil samples.

  19. Why are so many arc magmas close to 238U- 230Th radioactive equilibrium?

    NASA Astrophysics Data System (ADS)

    Condomines, Michel; Sigmarsson, Olgeir

    1993-09-01

    New analyses of 238U- 230Th disequilibria are reported for four active volcanoes: Merapi and Krakatoa in the Sunda arc (Indonesia), Masaya in Central America (Nicaragua), and Ambrym in the New Hebrides island arc. Despite a large range in ( 230Th /232Th ) ratios (from 0.65 in Merapi andesites to 2.5 in Masaya basalts), 238U and 230Th are close to radioactive equilibrium, as in many other arc magmas. In several mantle sources, Th/U ratios have clearly been modified by metasomatic processes associated with subduction. This is demonstrated in Central America by the correlation between ( 230Th /232Th ) and 10Be /9Be ratios for several active volcanoes along the arc. It is proposed that the 238U- 230Th radioactive equilibrium found in many arc magmas is the result of disequilibrium melting involving an easily melted, slab-derived, metasomatic component which dominates the uranium and thorium budget of the mantle sources. The departure from equilibrium may be either due to mixing with 230Th enriched melts derived from unmetasomatized mantle sources or to a late stage uranium addition by fluids. This latter process, producing uranium enriched magmas, has a greater influence in uranium and thorium poor magmas.

  20. Studies of positron electron pair production in {sup 238}U + {sup 232}Th

    SciTech Connect

    Ahmad, I.; Back, B.B.; Betts, R.R.

    1995-08-01

    Following the non-observation of sharp sum-energy lines in our earlier {sup 238}U + {sup 181}Ta measurements, it was decided to pursue measurements of the {sup 238}U + {sup 232}Th system which, in the previously published work, showed the most striking evidence for near-equal-energy back-to-back pairs leading to sharp sum-energy lines. Following the refurbishing of the APEX silicon arrays and extensive tests of the rotating target wheel assembly, a major positron run took place in November 1994. Rolled 1-mg/cm{sub 2} {sup 232}Th targets were bombarded with 5.95-MeV/u {sup 238}U. The target rotation allowed up to 2 pnA of beam to be used without serious deterioration of the targets. Over 300,000 pairs were accumulated, representing an order-of-magnitude improvement in statistics over the previously published results. Preliminary analysis shows no evidence for the sharp lines at a cross section level orders of magnitude below those previously reported. The analysis of these data is currently being completed in preparation for publication.

  1. Natural radionuclides measurements and total dose indicative evaluation in drinking waters of an Italian central region.

    PubMed

    Borio, Rita; Rongoni, Alba; Saetta, Daniela; Desideri, Donatella; Meli, Maria Assunta; Feduzi, Laura

    2007-09-01

    A study of radioactivity content in drinking waters collected in some areas of geological interest in an Italian central region was performed to check the compliance with recent European regulations. Gross alpha and beta activities, 226Ra, 238U, 234U, 210Po and 3H concentrations were measured. Gross alpha and beta, 226Ra and 3H activities were determined using an ultra-low-level scintillation counter, 238U, 234U and 210Po by alpha spectrometry after radiochemical separation. Recommended WHO guideline activity concentrations for drinking water were exceeded in 6 cases for gross alpha activity and were not exceeded in any case for gross beta activity. Tritium concentration was always lower than MDA (6.75 Bq L(-1)); the concentrations (mBq L(-1)) of 226Ra, 238U, 234U and 210Po ranged from <1.80 to 23.00, from 1.20 to 140.00, from 1.60 to 120.00 and from 0.25 to 5.90, respectively. Due to the importance of the water in human diet, the doses were calculated for children and adults using the dose coefficient factors reported by EC Directive 96/29 EURATOM and annual water intake; all samples furnished a dose lower the reference level for drinking water (0.1 mSv y(-1)).

  2. 230Th-234U Model-Ages of Some Uranium Standard Reference Materials

    SciTech Connect

    Williams, R W; Gaffney, A M; Kristo, M J; Hutcheon, I D

    2009-05-28

    The 'age' of a sample of uranium is an important aspect of a nuclear forensic investigation and of the attribution of the material to its source. To the extent that the sample obeys the standard rules of radiochronometry, then the production ages of even very recent material can be determined using the {sup 230}Th-{sup 234}U chronometer. These standard rules may be summarized as (a) the daughter/parent ratio at time=zero must be known, and (b) there has been no daughter/parent fractionation since production. For most samples of uranium, the 'ages' determined using this chronometer are semantically 'model-ages' because (a) some assumption of the initial {sup 230}Th content in the sample is required and (b) closed-system behavior is assumed. The uranium standard reference materials originally prepared and distributed by the former US National Bureau of Standards and now distributed by New Brunswick Laboratory as certified reference materials (NBS SRM = NBL CRM) are good candidates for samples where both rules are met. The U isotopic standards have known purification and production dates, and closed-system behavior in the solid form (U{sub 3}O{sub 8}) may be assumed with confidence. We present here {sup 230}Th-{sup 234}U model-ages for several of these standards, determined by isotope dilution mass spectrometry using a multicollector ICP-MS, and compare these ages with their known production history.

  3. Isotope fractionation of 238U and 235U during biologically-mediated uranium reduction

    NASA Astrophysics Data System (ADS)

    Stirling, Claudine H.; Andersen, Morten B.; Warthmann, Rolf; Halliday, Alex N.

    2015-08-01

    A series of laboratory-controlled microbial experiments using gram-negative sulphate-reducing bacteria (Desulfovibrio brasiliensis) inoculated with natural uranium were performed to investigate 238U/235U fractionation during bacterially-mediated U reduction. Control experiments, without bacteria to drive U reduction, were conducted in parallel. Paired measurements of 238U/235U and U concentration for both the residual growth medium solution and the accumulated biologically-mediated precipitate were obtained using multiple-collector inductively coupled plasma mass spectrometry (MC-ICPMS). The control experiments show that only minor (<0.1‰), if any 238U/235U fractionation occurs during co-precipitation with calcite. This implies that carbonate sediments are capable of faithfully recording the signature of the global ocean during Earth's major climatic events, including oxygenation and de-oxygenation transitions in the marine environment. The results for the microbial experiments demonstrate that the 238U/235U composition of the unreacted growth medium containing U(VI) is isotopically lighter than the composition of the U(IV)-bearing precipitate as U(VI) is consumed, in agreement with field-based observations of microbially-mediated U reduction. Uranium isotopic shifts of up to 0.8‰ were observed between the liquid and solid phases. These observations can be modelled using a Rayleigh distillation approach describing kinetic uptake in a closed system, which yields a fractionation factor α of 0.99923 ± 0.00004 (ε = -0.77 ± 04‰) for U(VI)-U(IV) reduction mediated by the D. brasiliensis microbe. This fractionation behaviour is consistent with that observed in field-based redox environments, which give rise to similar α values. Competing processes such as U co-precipitation (e.g. adsorption) may act to lower the apparent value for α and possibly play a secondary role both in the microbial experiments of this study and in natural U reduction settings where

  4. Radium uptake during barite recrystallization at 23 ± 2 °C as a function of solution composition: An experimental 133Ba and 226Ra tracer study

    NASA Astrophysics Data System (ADS)

    Curti, E.; Fujiwara, K.; Iijima, K.; Tits, J.; Cuesta, C.; Kitamura, A.; Glaus, M. A.; Müller, W.

    2010-06-01

    High-purity synthetic barite powder was added to pure water or aqueous solutions of soluble salts (BaCl 2, Na 2SO 4, NaCl and NaHCO 3) at 23 ± 2 °C and atmospheric pressure. After a short pre-equilibration time (4 h) the suspensions were spiked either with 133Ba or 226Ra and reacted under constant agitation during 120-406 days. The pH values ranged from 4 to 8 and solid to liquid (S/L) ratios varied from 0.01 to 5 g/l. The uptake of the radiotracers by barite was monitored through repeated sampling of the aqueous solutions and radiometric analysis. For both 133Ba and 226Ra, our data consistently showed a continuous, slow decrease of radioactivity in the aqueous phase. Mass balance calculations indicated that the removal of 133Ba activity from aqueous solution cannot be explained by surface adsorption only, as it largely exceeded the 100% monolayer coverage limit. This result was a strong argument in favor of recrystallization (driven by a dissolution-precipitation mechanism) as the main uptake mechanism. Because complete isotopic equilibration between aqueous solution and barite was approached or even reached in some experiments, we concluded that during the reaction all or substantial fractions of the initial solid had been replaced by newly formed barite. The 133Ba data could be successfully fitted assuming constant recrystallization rates and homogeneous distribution of the tracer into the newly formed barite. An alternative model based on partial equilibrium of 133Ba with the mineral surface (without internal isotopic equilibration of the solid) could not reproduce the measured activity data, unless multistage recrystallization kinetics was assumed. Calculated recrystallization rates in the salt solutions ranged from 2.8 × 10 -11 to 1.9 × 10 -10 mol m -2 s -1 (2.4-16 μmol m -2 d -1), with no specific trend related to solution composition. For the suspensions prepared in pure water, significantly higher rates (˜5.7 × 10 -10 mol m -2 s -1 or ˜49 μmol m

  5. Monte Carlo and deterministic simulations of activation ratio experiments for 238U(n,f), 238U(n,g) and 238U(n,2n) in the Big Ten benchmark critical assembly

    SciTech Connect

    Descalle, M; Clouse, C; Pruet, J

    2009-07-28

    The authors have compared calculations of critical assembly activation ratios using 3 different Monte Carlo codes and one deterministic code. There is excellent agreement. Discrepancies between the different Monte Carlo codes are the 1-2% level. Notably, the deterministic calculations with 87 groups are also in good agreement with the continuous energy Monte Carlo results. The three codes underestimate the {sup 238}U(n,f) reaction, suggesting that there is room for improvement in the evaluation, or in the evaluations of other reactions influencing the spectrum in BigTen. Until statistical uncertainties are implemented in Mercury, they strongly advise long runs to guarantee sufficient convergence of the flux at high energies, and they strongly encourage comparing Mercury results to a well-developed and documented code such as MCNP5 and/or COG. It may be that ENDL2008 will be available for use in COG within a year. Finally, it may be worthwhile to add a 'standard' reaction rate tally similar to those implemented in COG and MCNP5, if the goal is to expand the central fission and activation ratios simulations to include isotopes that are not part of the specifications for the assembly material composition.

  6. Duration of gas accumulation before the 2010 Eyjafjallajökull eruption constrained by 210Po-210Pb-226Ra disequilibria

    NASA Astrophysics Data System (ADS)

    Sigmarsson, Olgeir; Gauthier, Pierre-Jean; Condomines, Michel

    2014-05-01

    Excess gas phase in magmas erupting explosively is well known world-wide. However, the origin of this gas phase, in excess of what can be dissolved in the erupting magma at depth, and the duration of gas accumulation, is less well defined. The 2010 mildly explosive eruption at Eyjafjallajökull, Iceland, produced mingled tephra of benmoreiitic and trachytic composition whereas alkali basalt (MgO > 8 %) was emitted during the preceding flank eruption. The silicic tephra of the first explosive phase is composed of three glass types, alkaline rhyolite, mixed benmoreiite, and evolved basalt (MgO < 5 %). The rhyolitic glass is indistinguishable from tephra glass composition emitted during the penultimate eruption of Eyjafjallajökull in 1821-23 AD (Sigmarsson et al., 2011). Tephra from the first explosive phase, emitted on 15 and 17 April, had large 210Po in excess of 210Pb ((210Po/210Pb)0 as high as 2!) and a small, but significant, 210Pb excess over its parent 226Ra ((210Pb/226Ra)0= 1.05 and 1.04, respectively). These excesses suggest rapid accumulation of Po and Rn together with the major gas species in the residual rhyolitic magma from the 1821-23 eruption. The gas most likely originates from the basalt recharge that eventually provoked the eruption. Basalts emitted a month earlier during the flank eruption at Fimmvörðuháls lost all their Po upon eruption and had (210Po/210Pb)0 equal to 0). From a simple model of radon and polonium degassing and accumulation, the mass of basalt magma degassing over the mass of silicic magma accumulating the excess gas can be calculated. Moreover, the duration of gas accumulation can be shown to be close to 300 days. This duration suggests that gas was liberated from the basaltic magma since June 2009, a month that corresponds to the initial seismic swarm beneath Eyjafjallajökull preceding the explosive eruption of 14 April 2010.

  7. Determination of specific activity of (226)Ra, (232)Th and (40)K for assessment of radiation hazards from Turkish pumice samples.

    PubMed

    Turhan, Seref; Gündüz, Lüfullah

    2008-02-01

    The specific activity of (226)Ra, (232)Th and (40)K in 52 Turkish pumice samples collected from 11 geographical areas located in Central Anatolia, Eastern Anatolia, Mediterranean and Aegean regions was determined by gamma-ray spectrometry with a high-purity germanium (HPGe) detector. The specific activity of (226)Ra, (232)Th and (40)K ranged from 12.7+/-0.5 to 256.2+/-9.1Bqkg(-1) with a mean of 89.1+/-65.2Bqkg(-1), 12.3+/-1.0 to 237.9+/-12.2Bqkg(-1) with a mean of 87.0+/-61.4Bqkg(-1) and 300.1+/-5.5 to 1899.0+/-30.8Bqkg(-1) with a mean of 1211.9+/-419.8Bqkg(-1), respectively. Elemental concentrations were determined for U (from 1.0 to 20.7ppm with a mean of 7.2+/-5.3ppm), Th (from 3.0 to 58.6ppm with a mean of 21.4+/-15.1ppm) and K (from 1.0 to 6.1% with a mean of 3.9+/-1.3%). The radium equivalent activity (Ra(eq)), the activity index, the emanation coefficient, the (222)Rn mass exhalation rate, the indoor absorbed dose rate and the effective dose rate were estimated for the radiation hazard of the natural radioactivity in all samples. The calculated mean Ra(eq) value was 306.6+/-177.7Bqkg(-1) (54.6+/-5.5 to 737.6+/-49.0Bqkg(-1)) for all pumice samples. This value is lower than the recommended limit value of 370Bqkg(-1) for building raws and products. The emanation coefficient and the (222)Rn mass exhalation rate of all samples ranged from 29.4 to 42.9% with a mean of 36.2% and from 11.0 to 196.4microBqkg(-1)s(-1) with a mean of 73.5microBqkg(-1)s(-1), respectively. The mean indoor absorbed dose rate and the corresponding mean effective dose rate were 274.6+/-153.6nGyh(-1) (50.4-644.6nGyh(-1)) and 1.35+/-0.75mSvy(-1) (0.24-3.16mSvy(-1)), respectively. For all pumice samples the mean indoor absorbed dose rate is about three times higher than the population-weighted average of 84nGyh(-1), while the mean effective dose rate values except for PUM 05, PUM 06, PUM 10 and PUM 15 exceed the dose criterion of 1mSvy(-1).

  8. Investigating groundwater properties in high annual recharge rate aquifers using 14c and 226ra : example of the fontainebleau sands aquifer (paris basin, france)

    NASA Astrophysics Data System (ADS)

    Chabault, C.; Barbecot, F.; Ghaleb, B.; Dever, L.

    2003-04-01

    Aquifers with high annual recharge rates constitute prominent groundwater resource for freshwater supplies. However, they are very sensitive to pollutants. Moreover, in such cases, the establishment of recharge rates based on radiometric age measurements requires specific methodological approaches as in the example of the aquifer of the Fontainebleau Sands, in the Paris Basin, that we investigate here. It constitutes one of the major aquifers exploited for freshwater supply in the area. It is part of the Beauce aquifer that is underlain by the Romainville aquitard (green clays of Lower Sannoisian age) and overlain by millstone clays of Plio-Quaternary age. The Fontainebleau Sands aquifer outcrops principally in valleys, in the southern part of the Paris Basin (1). Groundwaters from the Fontainebleau Sands aquifer were sampled along a flow-path line in order to determine their geochemical evolution through time. Chemical and stables isotope compositions provide information on mineralisation processes during recharge. They indicate either carbonate dissolution up to saturation during the recharge or addition of recent water along the flow lines. These two possibilities will be discriminated using time tracers. 14C-derived age estimates (T1/2 = 5750 years) are not precise enough to assess residence times of recent waters. We will tentatively use 226 Ra measurements (T1/2 = 1620 years) to add constraints on age-estimates. 14C vs. 226Ra age models already tested in the Astian aquifer from southern France (2), are expected to provide further information on water-rock interactions occurring within the aquifer of the Fontainebleau Sands. (1) Bariteau. A., 1996, Modélisation géochimique d’un aquifère, la nappe de l’oligocène en Beauce et l’altération des Sables de Fontainebleau. Ecoles des Mines de Paris, pp. 179 (2) Barbecot, F., Dever, L., Hillaire-Marcel, C., Gibert, E., Travi, Y. And Marlin, C., 1999. Isotopic evidence for geochemical provinces in the Astian

  9. Generation of 238U Covariance Matrices by Using the Integral Data Assimilation Technique of the CONRAD Code

    NASA Astrophysics Data System (ADS)

    Privas, E.; Archier, P.; Bernard, D.; De Saint Jean, C.; Destouche, C.; Leconte, P.; Noguère, G.; Peneliau, Y.; Capote, R.

    2016-02-01

    A new IAEA Coordinated Research Project (CRP) aims to test, validate and improve the IRDF library. Among the isotopes of interest, the modelisation of the 238U capture and fission cross sections represents a challenging task. A new description of the 238U neutrons induced reactions in the fast energy range is within progress in the frame of an IAEA evaluation consortium. The Nuclear Data group of Cadarache participates in this effort utilizing the 238U spectral indices measurements and Post Irradiated Experiments (PIE) carried out in the fast reactors MASURCA (CEA Cadarache) and PHENIX (CEA Marcoule). Such a collection of experimental results provides reliable integral information on the (n,γ) and (n,f) cross sections. This paper presents the Integral Data Assimilation (IDA) technique of the CONRAD code used to propagate the uncertainties of the integral data on the 238U cross sections of interest for dosimetry applications.

  10. Potential human health risk by metal(loid)s, 234,238U and 210Po due to consumption of fish from the "Luis L. Leon" Reservoir (Northern México).

    PubMed

    Luna-Porres, Mayra Y; Rodríguez-Villa, Marco A; Herrera-Peraza, Eduardo F; Renteria-Villalobos, Marusia; Montero-Cabrera, María E

    2014-06-25

    Concentrations of As, Cu, Fe, Hg, Pb and Zn and activity concentrations from 234,238U and 210Po in water, fillet, liver and gills were determined in three stocked fish species from the Luis L. Leon reservoir, located in Northern Mexico. The considered species were Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus. 238U and 234U activity concentration (AC) in fillet samples showed values of 0.007-0.014 and 0.01-0.02 Bq∙kg-1 wet weight (ww), respectively. Liver samples for L. cyanellus, C. carpio and I. furcatus present 210Po AC of 1.16-3.26, 0.70-1.13 and 0.93-1.37 Bq∙kg-1 ww. Arsenic, mercury and lead concentration intervals in fillet samples were 0.13-0.39, 0.005-0.126 and 0.009-0.08 mg∙kg-1 ww, respectively, while in gill samples they were 0.11-0.43, 0.002-0.039 and 0.02-0.26 mg∙kg-1 ww. The elemental Bioaccumulation Factor (BAF) for fish tissues with respect to their concentrations in water was determined. L. cyanellus showed the highest BAF values for As and total U, being BAFAs = 37 and 40 L∙kg-1 in fillet and gills, respectively, and BAFU total = 1.5 L∙kg-1 in fillet. I. furcatus showed the highest BAF values for Hg and Pb, being BAFHg = 40 and 13 L∙kg-1 in fillet and gills, and BAFPb = 6.5 and 22 L∙kg-1 in fillet and gills, respectively. Some metal(loid) concentrations are slightly higher than European regulations for fish fillets. The difference in concentrations of metal(loid)s in fillet among the studied species is probably due to their differences in diet and habitat.

  11. Activity concentrations of 226Ra, 232Th, 40K and 137Cs radionuclides in Turkish medicinal herbs, their ingestion doses and cancer risks

    NASA Astrophysics Data System (ADS)

    Parmaksız, Aydın; Ağuş, Yusuf

    2014-11-01

    Twenty-two medicinal herb samples, each representing a distinct species, were collected from Turkish markets and measured by the gamma spectrometric method. The activity concentration of 226Ra in medicinal herbs was found in the range of minimum detectable activity (MDA) and 15.1 ± 2.2 Bqkg-1. The activity concentration of 232Th ranged from MDA values to 3.5 ± 0.8 Bqkg-1. The activity concentration of 40K varied between 50.0 ± 16.8 and 1311.5 ± 57.3 Bqkg-1. All 137Cs activity concentrations of medicinal herbs were found to have lower than MDA values. The bone surface dose, lower large intestine and colon doses were found to be 182.9, 18.8 and 18.7 µSvy-1, respectively. The highest committed effective dose originated from the annual ingestion of 1 kg medicinal herb was calculated notably low as 9.0 µSv. The cancer risk of ingestion of medicinal herbs was found to be small enough to be neglected. The selected Turkish medicinal herbs are considered safe for human consumption.

  12. Relative radiosensitivity of bone tumor induction among beagles as a function of age at injection of {sup 239}Pu or {sup 226}Ra

    SciTech Connect

    Lloyd, R.D.; Taylor, G.N.; Jee, W.S.S.; Miller, S.C.

    1999-01-01

    A comparison was made of the response to induction of skeletal malignancy from exposure of beagles to monomeric {sup 239}Pu or to {sup 226}Ra as juveniles (3 mo of age), young adults (1.5 y of age), or mature adults (5 y of age). This indicated that of these age groups, animals injected as young adults are most sensitive per Gy of average skeletal dose evaluated at 1 y before death. Dogs exposed either as juveniles or as mature adults appeared to be less sensitive. Relative radiosensitivities (RRS) of juvenile and mature beagles ranged between about 0.3 and 0.7 that of dogs injected as young adults. Mean values of RRS for both radionuclides were about 0.5, but RRS values derived from dogs given monomeric {sup 239}Pu appeared to be most reliable and were 0.27 {+-} 0.09 for dogs injected as juveniles and 0.41 {+-} 0.13 for animals exposed as mature adults.

  13. Current (1984) status of the study of /sup 226/Ra and /sup 228/Ra in humans at the Center for Human Radiobiology

    SciTech Connect

    Rundo, J.; Keane, A.T.; Lucas, H.F.; Schlenker, R.A.; Stebbings, J.H.; Stehney, A.F.

    1984-01-01

    The Center for Human Radiobiology has identified 5784 persons by name and type of exposure to /sup 226/Ra and /sup 228/Ra. Included are 4863 dial painters (mostly women) and non-laboratory employees of the radium dial industry, 410 laboratory workers, 399 persons who received radium for supposed therapeutic effects, and 112 in other categories. Body contents of radium have been measured in 1916 of the dial workers and about one-half of the subjects in the other groups. Bone sarcomas, carcinomas of the paranasal sinuses and mastoids, and deterioration of skeletal tissue are still the only effects unequivocally attributable to internal radium. Excess leukemias have not been observed and other malignancies, if in excess, appear more likely to be related to external gamma radiation or radon than to internal radium. Positive correlations with radium burdens have been found for the incidence of benign exostoses among subjects exposed to radium before age 18 and for shortened latency of ocular cataracts. 26 references, 3 figures, 5 tables.

  14. Flank eruptions of Mt Etna during the Greek-Roman and Early Medieval periods: New data from 226Ra-230Th dating and archaeomagnetism

    NASA Astrophysics Data System (ADS)

    Branca, Stefano; Condomines, Michel; Tanguy, Jean-Claude

    2015-10-01

    In this paper, we present new data from 226Ra-230Th dating and archaeomagnetism with the aim of improving the knowledge of the flank eruptions that occurred at Mt Etna during the Greek-Roman and Early Medieval periods, as defined in the new geological map of the volcano. The combination of the two dating techniques demonstrates that three major flank eruptions occurred on the lower north and west flanks during Greek-Roman epochs, producing large scoria cones and extensive lava flows. In particular, the Mt Ruvolo and Mt Minardo events highly impacted the territory of the west flank, notably by damming the Simeto River. The new data of the Millicucco and Due Monti lava flows, on the lower north-east flank, indicate a younger age than their stratigraphic ages quoted in the 2011 geological map, since they occurred around 700 and 500 AD, respectively. None of the large flank eruptions occurring on the lower slopes of Etna during the Early Medieval age are reported in the historical sources. Overall, our paper shows that a comprehensive assessment of eruptions at Mount Etna in the last three millennia can only be achieved through a multidisciplinary approach.

  15. Uranium isotopes (U-234/U-238) in rivers of the Yukon Basin (Alaska and Canada) as an aid in identifying water sources, with implications for monitoring hydrologic change in arctic regions

    USGS Publications Warehouse

    Kraemer, Thomas F.; Brabets, Timothy P.

    2012-01-01

    The ability to detect hydrologic variation in large arctic river systems is of major importance in understanding and predicting effects of climate change in high-latitude environments. Monitoring uranium isotopes (234U and 238U) in river water of the Yukon River Basin of Alaska and northwestern Canada (2001–2005) has enhanced the ability to identify water sources to rivers, as well as detect flow changes that have occurred over the 5-year study. Uranium isotopic data for the Yukon River and major tributaries (the Porcupine and Tanana rivers) identify several sources that contribute to river flow, including: deep groundwater, seasonally frozen river-valley alluvium groundwater, and high-elevation glacial melt water. The main-stem Yukon River exhibits patterns of uranium isotopic variation at several locations that reflect input from ice melt and shallow groundwater in the spring, as well as a multi-year pattern of increased variability in timing and relative amount of water supplied from higher elevations within the basin. Results of this study demonstrate both the utility of uranium isotopes in revealing sources of water in large river systems and of incorporating uranium isotope analysis in long-term monitoring of arctic river systems that attempt to assess the effects of climate change.

  16. Depth profile of 236U/238U in soil samples in La Palma, Canary Islands

    PubMed Central

    Srncik, M.; Steier, P.; Wallner, G.

    2011-01-01

    The vertical distribution of the 236U/238U isotopic ratio was investigated in soil samples from three different locations on La Palma (one of the seven Canary Islands, Spain). Additionally the 240Pu/239Pu atomic ratio, as it is a well establish tool for the source identification, was determined. The radiochemical procedure consisted of a U separation step by extraction chromatography using UTEVA® Resin (Eichrom Technologies, Inc.). Afterwards Pu was separated from Th and Np by anion exchange using Dowex 1x2 (Dow Chemical Co.). Furthermore a new chemical procedure with tandem columns to separate Pu and U from the matrix was tested. For the determination of the uranium and plutonium isotopes by alpha spectrometry thin sources were prepared by microprecipitation techniques. Additionally these fractions separated from the soil samples were measured by Accelerator Mass Spectrometry (AMS) to get information on the isotopic ratios 236U/238U, 240Pu/239Pu and 236U/239Pu, respectively. The 236U concentrations [atoms/g] in each surface layer (∼2 cm) were surprisingly high compared to deeper layers where values around two orders of magnitude smaller were found. Since the isotopic ratio 240Pu/239Pu indicated a global fallout signature we assume the same origin as the probable source for 236U. Our measured 236U/239Pu value of around 0.2 is within the expected range for this contamination source. PMID:21481502

  17. Oceanic stratified euphotic zone as elucidated by /sup 234/Th:/sup 238/U disequilibria

    SciTech Connect

    Coale, K.H.; Bruland, K.W.

    1987-01-01

    Profiles of dissolved and particulate /sup 234/Th were determined at the VERTEX 2 and 3 stations off Manzanillo, Mexico, and at the VERTEX 4 station about 900 km north of Hawaii. By modeling the disequilibria between /sup 234/Th and /sup 238/U in the dissolved and particulate form, estimates of scavenging rates for Th from the dissolved to particulate phases, particle residence times, and the flux of Th via particle removal can be obtained. /sup 234/Th:/sup 238/U activity ratio profiles indicate that the euphotic zone can be separated into two layers: an upper oligotrophic layer characterized by low new production values, low net scavenging, and long dissolved /sup 234/Th residence times; and a subsurface eutrophic layer with higher new production values, more intense scavenging, and shorter dissolved /sup 234/Th residence times. New production, rather than total primary production may determine net scavenging rates of reactive elements from oceanic surface waters. These results contribute to the emerging descriptions of the layered structure of oligotrophic euphotic zones and support the notion that this may be a general and ubiquitous feature of global stratified oligotrophic regimes.

  18. Photofission product yields of 238U and 239Pu with 22-MeV bremsstrahlung

    NASA Astrophysics Data System (ADS)

    Wen, Xianfei; Yang, Haori

    2016-06-01

    In homeland security and nuclear safeguards applications, non-destructive techniques to identify and quantify special nuclear materials are in great demand. Although nuclear materials naturally emit characteristic radiation (e.g. neutrons, γ-rays), their intensity and energy are normally low. Furthermore, such radiation could be intentionally shielded with ease or buried in high-level background. Active interrogation techniques based on photofission have been identified as effective assay approaches to address this issue. In designing such assay systems, nuclear data, like photofission product yields, plays a crucial role. Although fission yields for neutron-induced reactions have been well studied and readily available in various nuclear databases, data on photofission product yields is rather scarce. This poses a great challenge to the application of photofission techniques. In this work, short-lived high-energy delayed γ-rays from photofission of 238U were measured in between linac pulses. In addition, a list-mode system was developed to measure relatively long-lived delayed γ-rays from photofission of 238U and 239Pu after the irradiation. Time and energy information of each γ-ray event were simultaneously recorded by this system. Cumulative photofission product yields were then determined using the measured delayed γ-ray spectra.

  19. (238)U and total radioactivity in drinking waters in Van province, Turkey.

    PubMed

    Selçuk Zorer, Özlem; Dağ, Beşir

    2014-06-01

    As part of the national survey to evaluate natural radioactivity in the environment, concentration levels of total radioactivity and natural uranium have been analysed in drinking water samples. A survey to study natural radioactivity in drinking waters was carried out in the Van province, East Turkey. Twenty-three samples of drinking water were collected in the Van province and analysed for total α, total β and (238)U activity. The total α and total β activities were counted by using the α/β counter of the multi-detector low background system (PIC MPC-9604), and the (238)U concentrations were determined by inductively coupled plasma-mass spectrometry (Thermo Scientific Element 2). The samples were categorised according to origin: tap, spring or mineral supply. The activity concentrations for total α were found to range from 0.002 to 0.030 Bq L(-1) and for total β from 0.023 to 1.351 Bq L(-1). Uranium concentrations ranging from 0.562 to 14.710 μg L(-1) were observed in drinking waters. Following the World Health Organisation rules, all investigated waters can be used as drinking water.

  20. Photon-induced Fission Product Yield Measurements on 235U, 238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Krishichayan, Fnu; Bhike, M.; Tonchev, A. P.; Tornow, W.

    2015-10-01

    During the past three years, a TUNL-LANL-LLNL collaboration has provided data on the fission product yields (FPYs) from quasi-monoenergetic neutron-induced fission of 235U, 238U, and 239Pu at TUNL in the 0.5 to 15 MeV energy range. Recently, we have extended these experiments to photo-fission. We measured the yields of fission fragments ranging from 85Kr to 147Nd from the photo-fission of 235U, 238U, and 239Pu using 13-MeV mono-energetic photon beams at the HIGS facility at TUNL. First of its kind, this measurement will provide a unique platform to explore the effect of the incoming probe on the FPYs, i.e., photons vs. neutrons. A dual-fission ionization chamber was used to determine the number of fissions in the targets and these samples (along with Au monitor foils) were gamma-ray counted in the low-background counting facility at TUNL. Details of the experimental set-up and results will be presented and compared to the FPYs obtained from neutron-induced fission at the same excitation energy of the compound nucleus. Work supported in part by the NNSA-SSAA Grant No. DE-NA0001838.

  1. Physics of Neutron Interactions with 238U: New Developments and Challenges

    NASA Astrophysics Data System (ADS)

    Capote, R.; Trkov, A.; Sin, M.; Herman, M.; Daskalakis, A.; Danon, Y.

    2014-04-01

    The latest release of the EMPIRE-3.1 system (codename Rivoli) is being used in the advanced modeling of neutron induced reactions on the 238U nucleus with the aim of improving our knowledge of neutron scattering. The reaction model includes: (i) a new rotational-vibrational dispersive optical model potential coupling the low-lying collective bands of vibrational character observed in even-even actinides, (ii) the Engelbrecht-Weidenmüller transformation allowing for inclusion of compound-direct interference effects enhanced by a dispersive treatment of the optical model potential, (iii) a multi-humped fission barrier with absorption in the secondary well as described within the optical model for fission, and (iv) a modified Lorentzian model (MLO) of the radiative strength function. Impact of the advanced modeling on elastic and inelastic scattering cross section is being assessed by both comparison with selected microscopic experimental data and integral criticality benchmarks (e.g. FLATTOP, JEMIMA and BIGTEN assemblies). Benchmark calculations provide feedback to improve the reaction modeling and reduce both model and model-parameters uncertainties. Additionally, neutron scattering yields on 238U measured accurately at RPI by the time-of-flight technique at 29, 60, 112 and 153 degrees have been used as a further constraint on the incident energy dependence of elastic and inelastically scattered neutrons. Improvement of scattering cross sections in existing libraries is discussed.

  2. The low-energy dipole structure of 232Th , 236U and 238U actinide nuclei

    NASA Astrophysics Data System (ADS)

    Kuliev, A. A.; Guliyev, E.; Ertugral, F.; Özkan, S.

    2010-03-01

    In this study, ensuremath I^{π} = 1+ and ensuremath I^{π} = 1- dipole mode excitations are systematically investigated within the rotational and translational + Galilean invariant quasiparticle random-phase approximation for 232Th , 236U , and 238U actinide nuclei. It is shown that the investigated nuclei reach a B( M1) strength structure, which corresponds to the scissors mode. The calculated mean excitation energies as well as the summed B( M1) value of the scissors mode excitations are consistent with the available experimental data. The results of calculations indicate large differences to the rare-earth nuclei as is the case for the experiment: a doubling of the observed dipole strengths and a shift of the energy centroid to the lower energies by about 800keV. The calculations indicate the presence of a few prominent negative-parity ensuremath K^{π} = 1- states in the 2.0-4.0MeV energy interval. The occurrence of the negative-parity dipole states with the rather high B( E1) value less than 4MeV shows the necessity of explicit parity measurements for the correct determination of the scissors mode strength in 232Th , 236U , and 238U isotopes.

  3. Environmental characterization and radio-ecological impacts of non-nuclear industries on the Red Sea coast.

    PubMed

    El Mamoney, M H; Khater, Ashraf E M

    2004-01-01

    The Red Sea is a deep semi-enclosed and narrow basin connected to the Indian Ocean by a narrow sill in the south and to the Suez Canal in the north. Oil industries in the Gulf of Suez, phosphate ore mining activities in Safaga-Quseir region and intensified navigation activities are non-nuclear pollution sources that could have serious radiological impacts on the marine environment and the coastal ecosystems of the Red Sea. It is essential to establish the radiological base-line data, which does not exist yet, and to investigate the present radio-ecological impact of the non-nuclear industries to preserve and protect the coastal environment of the Red Sea. Some natural and man-made radionuclides have been measured in shore sediment samples collected from the Egyptian coast of the Red Sea. The specific activities of 226Ra and 210Pb (238U) series, 232Th series, 40K and 137Cs (Bq/kg dry weight) were measured using gamma ray spectrometers based on hyper-pure germanium detectors. The specific activities of 210Po (210Pb) and uranium isotopes (238U, 235U and 234U) (Bq/kg dry weight) were measured using alpha spectrometers based on surface barrier (PIPS) detectors after radiochemical separation. The absorbed radiation dose rates in air (nGy/h) due to natural radionuclides in shore sediment and radium equivalent activity index (Bq/kg) were calculated. The specific activity ratios of 228Ra/226Ra, 210Pb/226Ra, 226Ra/238U and 234U/238U were calculated for evaluation of the geo-chemical behaviour of these radionuclides. The average specific activity of 226Ra (238U) series, 232Th series, 40K and 210Pb were 24.7, 31.4, 427.5 and 25.6 Bq/kg, respectively. The concentration of 137Cs in the sediment samples was less than the lower limit of detection. The Red Sea coast is an arid region with very low rainfall and the sediment is mainly composed of sand. The specific activity of 238U, 235U and 234U were 25.3, 2.9 and 25.0 Bq/kg. The average specific activity ratios of 226Ra/228Ra, 210

  4. Ce-Fe-modified zeolite-rich tuff to remove Ba(2+)-like (226)Ra(2+) in presence of As(V) and F(-) from aqueous media as pollutants of drinking water.

    PubMed

    Olguín, María Teresa; Deng, Shuguang

    2016-01-25

    The sorption behavior of the Ba(2+)-like (226)Ra(2+) in the presence of H2AsO4(-)/HAsO4(2-) and F(-) from aqueous media using Ce-Fe-modified zeolite-rich tuff was investigated in this work. The Na-modified zeolite-rich tuff was also considered for comparison purposes. The zeolite-rich tuff collected from Wyoming (US) was in contact with NaCl and CeCl3-FeCl3 solutions to obtain the Na- and Ce-Fe-modified zeolite-rich tuffs (ZUSNa and ZUSCeFe). These zeolites were characterized by scanning electron microscopy and X-ray diffraction. The BET-specific surface and the points of zero charge were determined as well as the content of Na, Ce and Fe by neutron activation analysis. The textural characteristics and the point of zero charge were changed by the presence of Ce and Fe species in the zeolitic network. A linear model described the Ba(2+)-like (226)Ra(2+) sorption isotherms and the distribution coefficients (Kd) varied with respect to the metallic species present in the zeolitic material. The As(V) oxianionic chemical species and F(-) affected this parameter when the Ba(2+)-like (226)Ra(2+)-As(V)-F(-) solutions were in contact with ZUSCeFe. The H2AsO4(-)/HAsO4(2-) and F(-) were adsorbed by ZUSCeFe in the same amount, independent of the concentration of Ba(2+)-like (226)Ra(2+) in the initial solution.

  5. 230Th-234U Age-Dating Uranium by Mass Spectrometry

    SciTech Connect

    Williams, R W; Gaffney, A M

    2012-04-18

    This is the standard operating procedure used by the Isotope Ratio Mass Spectrometry Group of the Chemical Sciences Division at LLNL for the preparation of a sample of uranium oxide or uranium metal for {sup 230}Th-{sup 234}U age-dating. The method described here includes the dissolution of a sample of uranium oxide or uranium metal, preparation of a secondary dilution, spiking of separate aliquots for uranium and thorium isotope dilution measurements, and purification of uranium and thorium aliquots for mass spectrometry. This SOP may be applied to uranium samples of unknown purity as in a nuclear forensic investigation, and also to well-characterized samples such as, for example, U{sub 3}O{sub 8} and U-metal certified reference materials. The sample of uranium is transferred to a quartz or PFA vial, concentrated nitric acid is added and the sample is heated on a hotplate at approximately 100 C for several hours until it dissolves. The sample solution is diluted with water to make the solution approximately 4 M HNO{sub 3} and hydrofluoric acid is added to make it 0.05 M HF. A secondary dilution of the primary uranium solution is prepared. Separate aliquots for uranium and thorium isotope dilution measurements are taken and spiked with {sup 233}U and {sup 229}Th, respectively. The spiked aliquot for uranium isotope dilution analysis is purified using EiChrom UTEVA resin. The spiked aliquot for thorium isotope dilution analysis is purified by, first, a 1.8 mL AG1x8 resin bed in 9 M HCl on which U adsorbs and Th passes through; second, adsorbing Th on a 1 mL AG1x8 resin bed in 8 M HNO{sub 3} and then eluting it with 9 M HCl followed by 0.1 M HCl + 0.005 M HF; and third, by passing the Th through a final 1.0 mL AG1x8 resin bed in 9 M HCl. The mass spectrometry is performed using the procedure 'Th and U Mass Spectrometry for {sup 230}Th-{sup 234}U Age Dating'.

  6. Mount Etna eruptions of the last 2,750 years: revised chronology and location through archeomagnetic and 226Ra-230Th dating

    NASA Astrophysics Data System (ADS)

    Tanguy, Jean-Claude; Condomines, Michel; Le Goff, Maxime; Chillemi, Vito; La Delfa, Santo; Patanè, Giuseppe

    2007-09-01

    A careful re-examination of the well-known written documents pertaining to the 2,750-year-long historical period of Mount Etna was carried out and their interpretation checked through the high-accuracy archeomagnetic method (>1,200 large samples), combined with the 226Ra-230Th radiochronology. The magnetic dating is based upon secular variation of the direction of the geomagnetic field (DGF) and estimated to reach a precision of ±40 years for the last 1,200 years, and ±100 to 200 years up to circa 150 B.C. Although less precise, the 226Ra-230Th method provides a unique tool for distinguishing between historic and prehistoric lavas, which in some cases might have similar DGFs. We show that despite the abundance of details on ancient historical eruptions, the primary sources of information are often too imprecise to identify their lava flows and eruptive systems. Most of the ages of these lavas, which are today accepted on the geological maps and catalogues, were attributed in the 1800s on the basis of their morphology and without any stratigraphical control. In fact, we found that 80% of the “historically dated” flows and cones prior to the 1700s are usually several hundreds of years older than recorded, the discrepancies sometimes exceeding a millennium. This is proper the case for volcanics presumed of the “1651 east” (actually ˜1020), “1595” (actually two distinct flows, respectively, ˜1200 and ˜1060), “1566” (˜1180), “1536” (two branches dated ˜1250 and ˜950), “1444” (a branch dated ˜1270), “1408” (lower branches dated ˜450 and ˜350), “1381” (˜1160), “1329” (˜1030), “1284” (˜1450 and ˜700), “1169 or 812” (˜1000) eruptions. Conversely, well-preserved cones and flows that are undated on the maps were produced by recent eruptions that went unnoticed in historical accounts, especially during the Middle Ages. For the few eruptions that are recorded between A.D. 252 and 750 B.C., none of their presumed lava

  7. Compositional variation and 226Ra-230Th model ages of axial lavas from the southern Mid-Atlantic Ridge, 8°48'S

    NASA Astrophysics Data System (ADS)

    Haase, K. M.; Brandl, P. A.; Devey, C. W.; Hauff, F.; Melchert, B.; Garbe-Schönberg, D.; Kokfelt, T. F.; Paulick, H.

    2016-01-01

    We present geological observations and geochemical data for the youngest volcanic features on the slow spreading Mid-Atlantic Ridge at 8°48'S that shows seismic evidence for a thickened crust and excess magma formation. Young lava flows with high sonar reflectivity cover about 14 km2 in the axial rift and were probably erupted from two axial volcanic ridges each of about 3 km in length. Three different lava units occur along an about 11 km long portion of the ridge, and lavas from the northern axial volcanic ridge differ from those of the southern axial volcanic ridge and surrounding lava flows. Basalts from the axial rift flanks and from a pillow mound within the young flows are more incompatible element depleted than those from the young volcanic field. Lavas from this volcanic area have 226Ra-230Th disequilibria model ages of 1000 and 4000 years whereas the older lavas from the rift flank and the pillow mound, but also some of the lava field, are older than 8000 years. Glasses from the northern and southern ends of the southern lava unit indicate up to 100°C cooler magma temperatures than in the center and increased assimilation of hydrothermally altered material. The compositional heterogeneity on a scale of 3 km suggests small magma batches rising vertically from the mantle to the surface without significant lateral flow and mixing. The observations on the 8°48'S lava field support the model of low-frequency eruptions from single ascending magma batches that has been developed for slow spreading ridges.

  8. Comparative toxicity of /sup 226/Ra, /sup 239/Pu, /sup 241/Am, /sup 249/Cf, and /sup 252/Cf in C57BL/Do black and albino mice

    SciTech Connect

    Taylor, G.N.; Mays, C.W.; Lloyd, R.D.; Gardner, P.A.; Talbot, L.R.; McFarland, S.S.; Pollard, I.A.; Atherton, D.R.; VanMoorhem, D.; Brammer, D.

    1983-09-01

    Groups of C57BL/Do (black and albino) mice were injected with graded activities of /sup 226/Ra, /sup 239/Pu, /sup 241/Am, /sup 249/Cf, or /sup 252/Cf and were followed throughout life. Bone sarcoma was the principal radiation-induced end point, and the risks associated with average skeletal doses of the four transuranium radionuclides, relative to radium, were determined. The relative biological effectiveness (RBE) was calculated for each emitter by dividing its risk coefficient (bone sarcomas per 10(/sup 6/) mouse-rad) by the risk coefficient for /sup 226/Ra. Combined data for males and females in both black and albino mice gave the following values +/- SD for the RBE relative to /sup 226/Ra . 1.0: /sup 239/Pu . 15.3 +/- 3.9, /sup 241/Am . 4.9 +/- 1.4, /sup 249/Cf . 5.0 +/- 1.4, and /sup 252/Cf . 2.6 +/- 0.8. About 70% of the tumors occurred in the axial skeleton, and the risk coefficient for females averaged about four times higher than for males when all five nuclides were included. The RBE of fission fragment irradiation from /sup 252/Cf for cancer induction, relative to alpha irradiation, for the combined data in all of the animals given /sup 252/Cf and /sup 249/Cf, was 0.02 +/- 0.28, in agreement with the calculated theoretical value of 0.03, based on the ratio of summed track lengths in tissue.

  9. Comparative toxicity of /sup 226/Ra, /sup 239/Pu, /sup 241/Am, /sup 249/Cf, and /sup 252/Cf in C57BL/Do black and albino mice

    SciTech Connect

    Taylor, G.N.; Mays, C.W.; Lloyd, R.D.; Gardner, P.A.; TAlbot, L.R.; McFarland, S.S.; Pollard, T.A.; Atherton, D.R.; vanMoorhem, D.; Brammer, D.

    1983-09-01

    Groups of C57BL/Do (black and albino) mice were injected with graded activities of /sup 226/Ra, /sup 239/Pu, /sup 241/Am, /sup 249/Cf, or /sup 252/Cf and were followed throughout life. Bone sarcoma was the principal radiation-induced end point, and the risks associated with average skeletal doses of the four transuranium radionuclides, relative to radium, were determined. The relative biological effectiveness (RBE) was calculated for each emitter by dividing its risk coefficient (bone sarcomas per 10/sup 6/ mouse-rad) by the risk coefficient for /sup 226/Ra. Combined data for males and females in both black and albino mice gave the following values +- SD for the RBE relative to /sup 226/Ra = 1.0: /sup 239/Pu = 15.3 +- 3.9, /sup 241/Am = 4.9 +- 1.4, /sup 249/Cf = 5.0 +- 1.4, and /sup 252/Cf = 2.6 +- 0.8. About 70% of the tumors occurred in the axial skeleton, and the risk coefficient for females averaged about four times higher than for males when all five nuclides were included. The RBE of fission fragment irradiation from /sup 252/Cf for cancer induction, relative to ..cap alpha.. irradiation, for the combined data in all of the animals given /sup 252/Cf and /sup 249/Cf, was 0.02 +- 0.28, in agreement with the calculated theoretical value of 0.03, based on the ratio of summed track lengths in tissue.

  10. 238U and 235U isotope fractionation upon oxidation of uranium-bearing rocks by fracture waters

    NASA Astrophysics Data System (ADS)

    Chernyshev, I. V.; Golubev, V. N.; Chugaev, A. V.; Mandzhieva, G. V.

    2016-10-01

    The variations in 238U/235U values accompanying mobilization of U by fracture waters from uranium-bearing rocks, in which U occurs as a fine impregnation of oxides and silicates, were studied by the high-precision (±0.07‰) MC-ICP-MS method. Transition of U into the aqueous phase in the oxidized state U(VI) is accompanied by its isotope fractionation with enrichment of dissolved U(VI) in the heavy isotope 238U up to 0.32‰ in relation to the composition of the solid phases. According to the sign, this effect is consistent with the tendency of the behavior of 238U and 235U upon interaction of river waters with rocks of the catchment areas [11] and with the effect observed during oxidation of uraninite by the oxygen-bearing NaHCO3 solution [12].

  11. Evaluation of 238U Resonance Parameters from 0 to 20 keV

    SciTech Connect

    Derrien, H.; Leal, L.C.; Larson, N.; Courcelle, A.; Santamarina, A.

    2005-05-24

    The neutron resonance parameters of 238U were obtained in the energy range 0 to 20 keV from a sequential SAMMY analysis of the most recent high-resolution neutron transmission and neutron capture cross-section measurements. Special care was taken in the analysis of the lowest s-wave resonances leading to resonance parameters slightly different from those of ENDF/B-VI (Moxon-Sowerby resonance parameters). The resolved-resonance range was extended to 20 keV, taking advantage of the high-resolution neutron transmission data of Harvey and neutron capture data of Macklin et al. Preliminary integral tests were performed with the new resonance parameters; thermal low-enriched benchmark calculations show an improvement of the keff prediction, mainly due to a 1.5% decrease of the capture cross section at 0.0253 eV and about a 0.4% decrease of the effective shielded resonance capture integral.

  12. /sup 234/Th: /sup 238/U disequilibria within the California Current

    SciTech Connect

    Coale, K.H.; Bruland, K.W.

    1985-01-01

    Profiles of dissolved and particulate /sup 234/Th were determined at several stations within the California Current. Modeling of the disequilibria between the /sup 234/Th and /sup 238/U within the surface waters provides for estimates of the residence time of dissolved thorium with respect to particle scavenging, the particle residence time, and the particulate /sup 234/Th flux exiting the surface layer. The model-derived, first-order scavenging rate constant for dissolved thorium is observed to be proportional to the rate of primary production. Particle residence times seem to be governed by the rate of zooplankton grazing and the types of zooplankton present. Model-derived particulate /sup 234/Th fluxes are in good agreement with direct measurements by sediment traps.

  13. Photon scattering on /sup 238/U and the interpretation of near-threshold photofission resonances

    SciTech Connect

    Birenbaum, Y.; Alarcon, R.; Hoblit, S.D.; Laszewski, R.M.; Nathan, A.M.

    1987-10-01

    Cross sections for photon elastic scattering have been measured for /sup 238/U between 4.8 and 6.4 MeV with an energy resolution of about 50 keV. These data have been used along with existing photofission data to infer the total photoabsorption cross section sigma/sub T/ and the fission transmission coefficient T/sub f/ below neutron threshold. We find that the inferred sigma/sub T/ varies smoothly with energy and generally follows the extrapolated tail of the giant dipole resonance, and that T/sub f/ shows a broad bump between 5.6 and 5.9 MeV. These results strongly support the contention that resonances seen in near-threshold photofission cross sections are due to the fission and not the photon channel .

  14. Structure of N{>=}126 nuclei produced in fragmentation of {sup 238}U

    SciTech Connect

    Al-Dahan, N.; Podolyak, Zs.; Regan, P. H.; Steer, S. J.; Alkhomashi, N.; Gelletly, W.; Walker, P. M.; Farrelly, G.; Deo, A. Y.; Cullen, I. J.; Swan, T.; Bacelar, A. M. Denis; Gorska, M.; Pietri, S. B.; Gerl, J.; Domingo-Pardo, C.; Wollersheim, H. J.; Boutachkov, P.; Farinon, F.; Geissel, H.

    2009-01-28

    The nuclear structure of neutron-rich N{>=}126 nuclei have been investigated following their production via relativistic projectile fragmentation of a E/A = 1 GeV {sup 238}U beam on a Be target. The cocktail of secondary beam products were separated and identified using the GSI FRagment Separator (FRS). The nuclei of interest were implanted in a high-granularity active stopper detector set-up consisting of 6 double sided silicon strip detectors. The associated gamma-ray transitions were detected with the RISING array, consisting of 15 Euroball cluster Ge-detectors. Time-correlated gamma decays from individually identified nuclear species have been recorded, allowing the clean identification of isomeric decays.

  15. Multidimensional Skyrme-density-functional study of the spontaneous fission of 238U

    DOE PAGES

    Sadhukhan, J.; Mazurek, K.; Dobaczewski, J.; ...

    2015-01-01

    We determined the spontaneous fission lifetime of 238U by a minimization of the action integral in a three-dimensional space of collective variables. Apart from the mass-distribution multipole moments Q20 (elongation) and Q30 (left–right asymmetry), we also considered the pairing-fluctuation parameter λ2 as a collective coordinate. The collective potential was obtained self-consistently using the Skyrme energy density functional SkM*. The inertia tensor was obtained within the nonperturbative cranking approximation to the adiabatic time-dependent Hartree–Fock–Bogoliubov approach. As a result, the pairing-fluctuation parameter λ2 allowed us to control the pairing gap along the fission path, which significantly changed the spontaneous fission lifetime.

  16. Symmetric splitting for the system 32S+238U at energies near and below the barrier

    NASA Astrophysics Data System (ADS)

    Freifelder, R.; Braun-Munzinger, P.; Deyoung, P.; Schicker, R.; Sen, S.; Stachel, J.

    1987-06-01

    The total capture cross section for the system 32S+238U has been measured at energies from 0.93 to 1.08 times the s-wave interaction barrier by detecting coincident fission fragments following full momentum transfer reactions. The subbarrier cross section cannot be reproduced by a one-dimensional barrier penetration model. Using a quantum mechanical coupled channels model, good agreement is obtained. The measured angular distributions of fission fragments were compared to the predictions of saddle and scission point transition state theory. Saddle point transition state model calculations fail to reproduce the data, while scission point transition state calculations are in agreement with their qualitative trend. Evidence for nonequilibrium processes is presented.

  17. T-REX Design Considerations for Detection of Concealed 238U

    SciTech Connect

    Pruet, J; McNabb, D P

    2006-02-07

    Here they outline considerations that might inform choices for the design of a laser/linac-based light source used to detect {sup 238}U via excitation of the resonance at 680.11 keV in this isotope. They assume that the principal concern is speed of interrogation and not, e.g., how much radiological dose is imparted during a scan. It is found that if the photon detectors used in the system have an energy resolution better than or comparable to that of the interrogation beam, then to a first approximation the light source should be designed to have the highest possible specific fluence (photons per unit energy per unit time). there is also a weak dependence of scan time on the number of photons emitted per pulse of the light source. A simple formula describing the tradeoff between specific fluence and number of photons per pulse is presented.

  18. Studies of positron electron pair production in {sup 238}U + {sup 181}Ta

    SciTech Connect

    Ahmad, I.; Back, B.B.; Betts, R.R.

    1995-08-01

    Following the completion of APEX in late 1993, a two-week run on the {sup 238}U + {sup 181}Ta system at 6.1 and 6.3 MeV/u with 1 mg/cm{sup 2} targets provided, for the first time, data in which the expected sharp sum-energy lines should appear. Data from previous experiments show evidence for sharp sum-energy lines at 625, 748 and 805 keV, observed at bombarding energies from 5.9 to 6.3 MeV/u. The 625- and 809-keV lines display the characteristics of equal-energy back-to-back emission whereas the 748-keV line shows a rather different behavior. In our measurements, average beam currents of 2-3 pnA from the ATLAS accelerator were used to bombard 1-mg/cm{sup 2} rolled {sup 181}Ta targets, the energy loss in which corresponds to the ranges of bombarding energies over which the sharp sum-energy lines were previously reported. A run at 5.95 MeV/u for {sup 238}U + {sup 181}Ta followed in May 1994. These data were analyzed extensively. Sum-energy spectra measured in coincidence with scattered ions in the range 20{degrees} < {theta} < 68{degrees}. No evidence is found for the sharp sum-energy lines reported previously and, depending on the scenario assumed for the production mechanism and kinematics of the pairs, upper limits on cross sections at the 90% confidence limit range from 10-100 times smaller than the values that can be deduced from the earlier reports. We are in the process of refining the data analysis and simulations of the apparatus in order to finalize these numbers for publication.

  19. Neutron capture cross section measurements for 238U in the resonance region at GELINA

    NASA Astrophysics Data System (ADS)

    Kim, H. I.; Paradela, C.; Sirakov, I.; Becker, B.; Capote, R.; Gunsing, F.; Kim, G. N.; Kopecky, S.; Lampoudis, C.; Lee, Y.-O.; Massarczyk, R.; Moens, A.; Moxon, M.; Pronyaev, V. G.; Schillebeeckx, P.; Wynants, R.

    2016-06-01

    Measurements were performed at the time-of-flight facility GELINA to determine the 238U(n, γ) cross section in the resonance region. Experiments were carried out at a 12.5 and 60m measurement station. The total energy detection principle in combination with the pulse height weighting technique was applied using C6D6 liquid scintillators as prompt γ-ray detectors. The energy dependence of the neutron flux was measured with ionisation chambers based on the 10B(n, α) reaction. The data were normalised to the isolated and saturated 238U resonance at 6.67 eV. Special procedures were applied to reduce bias effects due to the weighting function, normalization, dead time and background corrections, and corrections related to the sample properties. The total uncertainty due to the weighting function, normalization, neutron flux and sample characteristics is about 1.5%. Resonance parameters were derived from a simultaneous resonance shape analysis of the GELINA capture data and transmission data obtained previously at a 42m and 150m station of ORELA. The parameters of resonances below 500 eV are in good agreement with those resulting from an evaluation that was adopted in the main data libraries. Between 500 eV and 1200 eV a systematic difference in the neutron width is observed. Average capture cross section data were derived from the experimental capture yield in the energy region between 3.5 keV and 90 keV. The results are in good agreement with an evaluated cross section resulting from a least squares fit to experimental data available in the literature prior to this work. The average cross section data derived in this work were parameterised in terms of average resonance parameters and included in a least squares analysis together with other experimental data reported in the literature.

  20. Neutron Capture Cross Sections and Gamma Emission Spectra from Neutron Capture on 234,236,238U Measured with DANCE

    NASA Astrophysics Data System (ADS)

    Ullmann, J. L.; Mosby, S.; Bredeweg, T. A.; Couture, A. J.; Haight, R. C.; Jandel, M.; Kawano, T.; O'Donnell, J. M.; Rundberg, R. S.; Vieira, D. J.; Wilhelmy, J. B.; Wu, C.-Y.; Becker, J. A.; Chyzh, A.; Baramsai, B.; Mitchell, G. E.; Krticka, M.

    2014-05-01

    A new measurement of the 238U(n, γ) cross section using a thin 48 mg/cm2 target was made using the DANCE detector at LANSCE over the energy range from 10 eV to 500 keV. The results confirm earlier measurements. Measurements of the gamma-ray emission spectra were also made for 238U(n, γ) as well as 234,236U(n, γ). These measurements help to constrain the radiative strength function used in the cross-section calculations.

  1. Uranium series disequilibrium and high thorium and radium enrichments in Karst formations

    SciTech Connect

    Gunten, H.R. von; Roessler, E.; Surbeck, H.

    1996-04-01

    We found, in limestone Karst soils of the Jura Mountains and of the mountains in the central part of Switzerland, an enrichment up to a factor 20 of {sup 230}Th and {sup 226}Ra with respect to the activities of their progenitors, {sup 234}U and {sup 238}U. Thus, a significant radioactive disequilibrium exists between {sup 238/234}U and {sup 230}Th and {sup 226}Ra. The enrichment of {sup 226}Ra leads to locally high concentrations of its decay product, the noble gas {sup 222}Rn. We propose continuous chemical weathering of limestone (calcite) fragments within the soil column as a plausible cause for the high {sup 230}Th, {sup 226}Ra, and {sup 222}Rn activities. Uranium, contained within calcite, is released during weathering and migrates as stable uranyl carbonate complexes through the soil column. In contrast, its decay products ({sup 230}Th and {sup 226}Ra) hydrolyze, are strongly sorbed to soil particles, and/or form insoluble compounds that become more and more enriched in the soil as this process continues in time. 39 refs., 3 figs., 5 tabs.

  2. U-series Disequilibria in Continental Arcs: NE Japan Case

    NASA Astrophysics Data System (ADS)

    Tepley, F. J.; Gill, J. B.; Williams, R. W.

    2005-12-01

    Basalts and andesites from continental arcs typically are close to equilibrium between (238U) and (230Th), and have subdued excesses of 226Ra compared to oceanic arcs (Turner et al., 2003). There is ambiguity whether these and other geochemical features derive from subducted sediment, subcontinental lithosphere, or the crust. We report new 238U-234U-230Th-226Ra data for 20 historical to Holocene samples from Asama in the south of NE Japan to Tarumai in the north. Most straddle the equiline with <5% excess U or Th, yet have 10-60% excess 226Ra. The only significant excess U occurs at Usu and Iwaki in the north where it correlates with higher (230Th)/(232Th) as in other arcs (e.g., Mariana). Otherwise (230Th)/(232Th) ratios are 0.75-1.05 which is less than in the surrounding Izu and Kurile oceanic arcs. Most ratios <0.95 are associated with trace element evidence of crustal contamination that drags samples down the equiline. The exception is Iwate where Th/U ratios are ~4.0 even in depleted basalts. Excess 226Ra is greater in basalts than andesites. The excess 226Ra, plus elevated 10Be and Th, is attributed to ubiquitous slab inputs that are overprinted by even higher Th contents from a crustal source with Th/U >4.

  3. Certified reference materials for radionuclides in Bikini Atoll sediment (IAEA-410) and Pacific Ocean sediment (IAEA-412).

    PubMed

    Pham, M K; van Beek, P; Carvalho, F P; Chamizo, E; Degering, D; Engeler, C; Gascó, C; Gurriaran, R; Hanley, O; Harms, A V; Herrmann, J; Hult, M; Ikeuchi, Y; Ilchmann, C; Kanisch, G; Kis-Benedek, G; Kloster, M; Laubenstein, M; Llaurado, M; Mas, J L; Nakano, M; Nielsen, S P; Osvath, I; Povinec, P P; Rieth, U; Schikowski, J; Smedley, P A; Suplinska, M; Sýkora, I; Tarjan, S; Varga, B; Vasileva, E; Zalewska, T; Zhou, W

    2016-03-01

    The preparation and characterization of certified reference materials (CRMs) for radionuclide content in sediments collected offshore of Bikini Atoll (IAEA-410) and in the open northwest Pacific Ocean (IAEA-412) are described and the results of the certification process are presented. The certified radionuclides include: (40)K, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (232)Th, (234)U, (238)U, (239)Pu, (239+240)Pu and (241)Am for IAEA-410 and (40)K, (137)Cs, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (232)Th, (235)U, (238)U, (239)Pu, (240)Pu and (239+240)Pu for IAEA-412. The CRMs can be used for quality assurance and quality control purposes in the analysis of radionuclides in sediments, for development and validation of analytical methods and for staff training.

  4. Sequential Determination of U and Th Decay Series in Santana Cave, Southwest Brazil

    SciTech Connect

    Silva, P. S. C.; Damatto, S. R.; Mazzilli, B. P.

    2008-08-07

    Parque Estadual Turistico do Alto Ribeira (PETAR) is located in the South-western part of Sao Paulo State, in the Ribeira Valley. In this national state park a large number of caves are found, which are among the most visited of the country. These caves, located in a karstic zone, are characterized by the presence of carbonaceous rocks frequently fractured and collapsed. Although, carbonates (dolomites and calcitic rocks) usually have low U content, this element can be found in the structure of the surrounding rocks. This paper aims to determine {sup 238}U, {sup 234}U, {sup 226}Ra and {sup 210}Pb concentration in samples of rock, soil, river water and sediment, in Santana cave. The radionuclide {sup 238}U was determined by alpha spectrometry using a surface barrier detector. {sup 226}Ra and {sup 210}Pb were determined by measuring the gross alpha and beta activity on a gas flow proportional counter.

  5. Sequential Determination of U and Th Decay Series in Santana Cave, Southwest Brazil

    NASA Astrophysics Data System (ADS)

    Silva, P. S. C.; Damatto, S. R.; Mazzilli, B. P.

    2008-08-01

    Parque Estadual Turístico do Alto Ribeira (PETAR) is located in the South-western part of São Paulo State, in the Ribeira Valley. In this national state park a large number of caves are found, which are among the most visited of the country. These caves, located in a karstic zone, are characterized by the presence of carbonaceous rocks frequently fractured and collapsed. Although, carbonates (dolomites and calcitic rocks) usually have low U content, this element can be found in the structure of the surrounding rocks. This paper aims to determine 238U, 234U, 226Ra and 210Pb concentration in samples of rock, soil, river water and sediment, in Santana cave. The radionuclide 238U was determined by alpha spectrometry using a surface barrier detector. 226Ra and 210Pb were determined by measuring the gross alpha and beta activity on a gas flow proportional counter.

  6. Natural radioactivity levels in mineral, therapeutic and spring waters in Tunisia

    NASA Astrophysics Data System (ADS)

    Labidi, S.; Mahjoubi, H.; Essafi, F.; Ben Salah, R.

    2010-12-01

    Radioactivity measurements were carried out in 26 groundwater samples from Tunisia. Activity concentrations of uranium were studied by radiochemical separation procedures followed by alpha spectrometry and that for radium isotopes by gamma-ray spectrometry. The results show that, the concentrations in water samples range from 1.2 to 69 mBq/L.1, 1.3 to 153.4 mBq/L, 2.0 to 1630.0 mBq/L and 2.0 to 1032.0 mBq/L for 238U, 234U, 226Ra and 228Ra, respectively. The U and Ra activity concentrations are low and similar to those published for other regions in the world. The natural radioactivity levels in the investigated samples are generally increased from mineral waters through therapeutic to the spring waters. The results show that a correlation between total dissolved solids (TDS) values and the 226Ra concentrations was found to be high indicating that 266Ra has a high affinity towards the majority of mineral elements dissolved in these waters. High correlation coefficients were also observed between 226Ra content and chloride ions for Cl --Na + water types. This can be explained by the fact that radium forms a complex with chloride and in this form is more soluble. The isotopic ratio of 234U/ 238U and 226Ra/ 234U varies in the range from 0.8 to 2.6 and 0.6 to 360.8, respectively, in all investigated waters, which means that there is no radioactive equilibrium between the two members of the 238U series. The fractionation of isotopes of a given element may occur because of preferential leaching of one, or by the direct action of recoil during radioactive decay. The annual effective doses due to ingestion of the mineral waters have been estimated to be well below the 0.1 mSv/y reference dose level.

  7. Effects of nuclear orientation on fusion and fission process for reactions using {sup 238}U target nucleus

    SciTech Connect

    Nishio, K.; Ikezoe, H.; Mitsuoka, S.; Nishinaka, I.; Makii, H.; Nagame, Y.; Watanabe, Y.; Ohtsuki, T.; Hirose, K.; Hofmann, S.

    2010-06-01

    Fission fragment mass distributions in the reaction of {sup 30}Si+{sup 238}U were measured at the energies around the Coulomb barrier. At the above-barrier energies, the mass distribution showed Gaussian shape. At the sub-barrier energies, asymmetric fission mode peaked at A{sub L}/A{sub H}approx =90/178 was observed. The asymmetric fission should be attributed to quasifission from the results of the measured evaporation residue (ER) cross-sections produced by {sup 30}Si+{sup 238}U. The cross-section for {sup 263}Sg at the above-barrier energy agree with the statistical model calculation which assumes that the measured fission cross-sections are equal to the fusion cross-sections, whereas the one for {sup 264}Sg measured at the sub-barrier energy is smaller than the calculation, indicating the presence for quasifission. The fragment mass distributions are compared to those for {sup 36}S+{sup 238}U and {sup 40}Ar+{sup 238}U.

  8. Combined 238U/235U and Pb Isotopics of Planetary Core Material: The Absolute Age of the IVA Iron Muonionalusta

    NASA Astrophysics Data System (ADS)

    Brennecka, G. A.; Amelin, Y.; Kleine, T.

    2016-08-01

    We report a measured 238U/235U for the IVA iron Muonionalusta. This measured value requires an age correction of ~7 Myr to the previously published Pb-Pb age. This has major implications for our understanding of planetary core formation and cooling.

  9. Time-dependent Hartree-Fock calculations for multinucleon transfer and quasifission processes in the 238U+64Ni reaction

    NASA Astrophysics Data System (ADS)

    Sekizawa, Kazuyuki; Yabana, Kazuhiro

    2016-05-01

    Background: Multinucleon transfer (MNT) and quasifission (QF) processes are dominant processes in low-energy collisions of two heavy nuclei. They are expected to be useful to produce neutron-rich unstable nuclei. Nuclear dynamics leading to these processes depends sensitively on nuclear properties such as deformation and shell structure. Purpose: We elucidate reaction mechanisms of MNT and QF processes involving heavy deformed nuclei, making detailed comparisons between microscopic time-dependent Hartree-Fock (TDHF) calculations and measurements for the 238U+64Ni reaction. Methods: Three-dimensional Skyrme-TDHF calculations are performed. Particle-number projection method is used to evaluate MNT cross sections from the TDHF wave function after collision. Results: Fragment masses, total kinetic energy (TKE), scattering angle, contact time, and MNT cross sections are investigated for the 238U+64Ni reaction. They show reasonable agreements with measurements. At small impact parameters, collision dynamics depends sensitively on the orientation of deformed 238U. In tip (side) collisions, we find a larger (smaller) TKE and a shorter (longer) contact time. In tip collisions, we find a strong influence of quantum shells around 208Pb. Conclusions: It is confirmed that the TDHF calculations reasonably describe both MNT and QF processes in the 238U64Ni reaction. Analyses of this system indicate the significance of the nuclear structure effects such as deformation and quantum shells in nuclear reaction dynamics at low energies.

  10. Mass yield distributions of fission products from photo-fission of 238U induced by 11.5-17.3 MeV bremsstrahlung

    NASA Astrophysics Data System (ADS)

    Naik, H.; Carrel, Frédérick; Kim, G. N.; Laine, Frédéric; Sari, Adrien; Normand, S.; Goswami, A.

    2013-07-01

    The yields of various fission products in the 11.5, 13.4, 15.0 and 17.3 MeV bremsstrahlung-induced fission of 238U have been determined by recoil catcher and an off-line γ-ray spectrometric technique using the electron linac, SAPHIR at CEA, Saclay, France. The mass yield distributions were obtained from the fission product yields using charge-distribution corrections. The peak-to-valley ( P/ V ratio, average light mass (< A L>) and heavy mass (< A H>) and average number of neutrons (< v>) in the bremsstrahlung-induced fission of 238U at different excitation energies were obtained from the mass yield data. From the present and literature data in the 238U ( γ, f ) and 238U ( n, f ) reactions at various energies, the following observations were obtained: i) The mass yield distributions in the 238U ( γ, f ) reaction at various energies of the present work are double-humped, similar to those of the 238U ( n, f ) reaction of comparable excitation energy. ii) The yields of fission products for A = 133-134, A = 138-140, and A = 143-144 and their complementary products in the 238U ( γ, f) reaction are higher than other fission products due to the nuclear structure effect. iii) The yields of fission products for A = 133-134 and their complementary products are slightly higher in the 238U ( γ, f ) than in the 238U ( n, f ) , whereas for A = 138-140 and 143-144 and their complementary products are comparable. iv) With excitation energy, the increase of yields of symmetric products and the decrease of the peak-to-valley ( P/ V ratio in the 238U ( γ, f) reaction is similar to the 238U ( n, f) reaction. v) The increase of < v> with excitation energy is also similar between the 238U ( γ, f ) and 238U ( n, f) reactions. However, it is surprising to see that the < A L> and < A H> values with excitation energy behave entirely differently from the 238U ( γ, f ) and 238U ( n, f ) reactions.

  11. Uranium stable isotope fractionation in the Black Sea: Modern calibration of the 238U/235U paleo-redox proxy

    NASA Astrophysics Data System (ADS)

    Rolison, John M.; Stirling, Claudine H.; Middag, Rob; Rijkenberg, Micha J. A.

    2017-04-01

    The isotopic compositions of redox-sensitive metals, including uranium (U), in marine sediments have recently emerged as powerful diagnostic tracers of the redox state of the ancient ocean-atmosphere system. Reliable interpretation of sedimentary isotopic information requires a thorough understanding of the environmental controls on isotopic fractionation in modern anoxic environments before being applied to the paleo-record. In this study, the relationship between ocean anoxia and the isotopic fractionation of U was investigated in the water column and sediments of the Black Sea, the world's largest anoxic basin. Paired measurements of 238U/235U and U concentration, supported by other redox parameters, were obtained for water column and sediment samples collected during the 2013 GA04N GEOTRACES expedition to the Black Sea. Removal of U from the water column occurs during the redox transition of soluble U(VI) to relatively insoluble U(IV), resulting in up to 43% of U being removed from solution in euxinic bottom waters. Uranium reduction and removal is accompanied by a progressive shift in 238U/235U towards isotopically light values in the water column as heavier 238U is preferentially exported to sediments over lighter 235U. This gives rise to apparent isotope enrichment factors of ε = -0.63 ± 0.09‰ and ε = -0.84 ± 0.11‰ when U removal is modelled by Rayleigh and closed system equilibrium isotope fractionation, respectively. These ε values fall within the range determined for bacterial U reduction experiments, and together with a striking correlation between the distributions of U and H2S, implicate microbially-mediated U(VI)-U(IV) reduction as the primary mechanism controlling U isotopic shifts in the Black Sea. The 238U/235U of underlying sediments is related to the the 238U/235U of Black Sea bottom waters through the isotope enrichment factor of the U reduction reaction but the relationship between sedimentary and water column 238U/235U is complicated

  12. 238U-230Th crystallization ages for the oldest domes of the Mono Craters, eastern California

    NASA Astrophysics Data System (ADS)

    Marcaida, M.; Vazquez, J. A.

    2014-12-01

    The Mono Craters volcanic chain is one of the youngest areas of rhyolitic volcanism in the Mono Lake-Long Valley region of eastern California. Located just south of Mono Lake, the Mono Craters comprise at least 28 individual domes and flows (numbered 3-30, north to south); however, the timing and frequency of eruptions remain poorly resolved. The earliest signs of volcanic activity are preserved as numerous tephra layers (Ashes 1-19, top to bottom) in the late Pleistocene Wilson Creek formation of ancestral Mono Lake, which indicate that rhyolitic volcanism from Mono Craters began by at least ca. 62 ka [1]. Although the current chronology indicates that most of the Mono Craters are younger than ca. 20 ka [2-4], similar compositions of titanomagnetite from both pumice and lava potentially correlate several Wilson Creek tephras to porphyritic biotite-bearing domes 11, 24, and 19 of the Mono Craters [5], suggesting that multiple domes in the Mono Craters chain reflect volcanism older than ca. 20 ka. Ash 3 is correlated to dome 11 based on similar ca. 20 ka ages and titanomagnetite compositions [6]. More recently, we performed ion microprobe 238U-230Th dating of unpolished rims of allanite and zircon from domes 24 and 19, yielding isochron ages of ca. 38 ka and ca. 42 ka, respectively. The age of dome 24 is consistent with the ca. 38 ka age of its potential correlative tephra layers [1, 5], indicating that dome 24 is likely the extrusive equivalent of Ashes 9-10. Dome 19 has titanomagnetite crystals with similar bimodal chemistry to titanomagnetites from Ash 15 [5]. The age of dome 19 is indistinguishable from the 238U-230Th age of Ash 15 [1], which erupted during a prominent geomagnetic excursion, originally designated as the "Mono Lake" excursion. Combining geochronological and titanomagnetite compositional data confirms that Ash 15 and its extrusive equivalent, dome 19, erupted during the Laschamp excursion. [1] Vazquez, J.A. and Lidzbarski, M.I. (2012) EPSL 357

  13. U-Th-Ra variations in Himalayan river sediments (Gandak river, India): Weathering fractionation and/or grain-size sorting?

    NASA Astrophysics Data System (ADS)

    Bosia, Clio; Chabaux, François; Pelt, Eric; France-Lanord, Christian; Morin, Guillaume; Lavé, Jérôme; Stille, Peter

    2016-11-01

    Understanding the origin of U-Th-Ra variations in the Ganga river sediments is a prerequisite for correctly using U-series nuclides to constrain the sediment transport times in Himalayan rivers. For this purpose, U, Th, and Ra concentrations, along with 238U-234U-230Th-226Ra radioactive disequilibria, were analyzed in bank, bedload and suspended sediments from the Gandak river, one of the main tributaries of the Ganga river. The data confirm that U and Th budgets of the Himalayan sediments are significantly influenced by minor resistant minerals, such as zircon, garnet and Ti-bearing minerals, the dissolution of which required the use of a high-pressure acid digestion process. Most importantly, the results indicate that the variations in (238U/232Th) and (230Th/232Th) activity ratios and 238U-234U-230Th-226Ra disequilibria in sediments along the river alluvial plain mainly reflect modifications in the mineralogical and grain-size compositions rather than the degree of weathering during transport. The (238U/232Th) and (230Th/232Th) activity ratios in the bank and bed sediments are related to variations in the minor primary minerals strongly enriched in U and Th (i.e., zircon, REE-bearing minerals and Ti-bearing minerals), whereas the activity ratios in the suspended load are related to variations in the proportions of clay, Fe-oxyhydroxides and the silt-sand fraction, which contains U- and Th-bearing minor minerals. The data also indicate that 238U-234U-230Th-226Ra disequilibria are strongly influenced by secondary mineral phases: the 230Th budget is likely mainly controlled by Fe-oxyhydroxides, and the 226Ra budget is likely mainly controlled by clay minerals. Therefore, the variations in the 238U-234U-230Th-232Th system in the sediments of the Gandak river cannot simply be interpreted as the result of fractionation due to chemical transformation of the bulk sediment during its transport within the alluvial plain and/or the result of radioactive decay. Consequently

  14. Timing of degassing and plagioclase growth in lavas erupted from Mount St. Helens, 2004-2005, from 210Po-210Pb-226Ra disequilibria: Chapter 37 in A volcano rekindled: the renewed eruption of Mount St. Helens, 2004-2006

    USGS Publications Warehouse

    Reagan, Mark K.; Cooper, Kari M.; Pallister, John S.; Thornber, Carl R.; Wortel, Matthew; Sherrod, David R.; Scott, William E.; Stauffer, Peter H.

    2008-01-01

    Disequilibrium between 210Po, 210Pb, and 226Ra was measured on rocks and plagioclase mineral separates erupted during the first year of the ongoing eruption of Mount St. Helens. The purpose of this study was to monitor the volatile fluxing and crystal growth that occurred in the weeks, years, and decades leading up to eruption. Whole-rock samples were leached in dilute HCl to remove 210Po precipitated in open spaces. Before leaching, samples had variable initial (210Po) values, whereas after leaching, the groundmasses of nearly all juvenile samples were found to have had (210Po) ≈ 0 when they erupted. Thus, most samples degassed 210Po both before and after the magmas switched from open- to closed-system degassing. All juvenile samples have (210Pb)/(226Ra) ratios within 2 δ of equilibrium, suggesting that the magmas involved in the ongoing eruption did not have strong, persistent fluxes of 222Rn in or out of magmas during the decades and years leading to eruption. These equilibrium values also require a period of at least a century after magma generation and the last significant differentiation of the Mount St. Helens dacites. Despite this, the elevated (210Pb)/(226Ra) value measured in a plagioclase mineral separate from lava erupted in 2004 suggests that a significant proportion of this plagioclase grew within a few decades of eruption. The combined dataset suggests that for most 2004-5 lavas, the last stage of open-system degassing of the dacite magmas at Mount St. Helens is confined to the period between 1-2 years and 1-2 weeks before eruption, whereas plagioclase large enough to be included in the mineral separate grew around the time of the 1980s eruption or earlier.

  15. 230Th/238U dating of hydrothermal sulfides from Duanqiao hydrothermal field, Southwest Indian Ridge

    NASA Astrophysics Data System (ADS)

    Yang, Weifang; Tao, Chunhui; Li, Huaiming; Liang, Jin; Liao, Shili; Long, Jiangping; Ma, Zhibang; Wang, Lisheng

    2016-11-01

    Duanqiao hydrothermal field is located between the Indomed and Gallieni fracture zones at the central volcano, at 50°28'E in the ultraslow-spreading Southwest Indian Ridge (SWIR). Twenty-eight subsamples from a relict chimney and massive sulfides were dated using the 230Th/238U method. Four main episodes of hydrothermal activity were determined according to the restricted results: 68.9-84.3, 43.9-48.4, 25.3-34.8, and 0.7-17.3 kyrs. Hydrothermal activity of Duanqiao probably started about 84.3 (±0.5) kyrs ago and ceased about 0.737 (±0.023) kyrs ago. The periodic character of hydrothermal activity may be related to the heat source provided by the interaction of local magmatism and tectonism. The estimated mean growth rate of the sulfide chimney is <0.02 mm/yr. This study is the first to estimate the growth rate of chimneys in the SWIR. The maximum age of the relict chimney in Duanqiao hydrothermal filed is close to that of the chimneys from Mt. Jourdanne (70 kyrs). The hydrothermal activity in Dragon Flag field is much more recent than that of Duanqiao or Mt. Jourdanne fields. The massive sulfides are younger than the sulfides from other hydrothermal fields such as Rainbow, Sonne and Ashadze-2. The preliminarily estimated reserves of sulfide ores of Duanqiao are approximately 0.5-2.9 million tons.

  16. Retardation of 238U and 232Th decay chain radionuclides in Long Island and Connecticut aquifers

    NASA Astrophysics Data System (ADS)

    Copenhaver, Sally A.; Krishnaswami, S.; Turekian, Karl K.; Epler, Nathan; Cochran, J. K.

    1993-02-01

    Knowledge of the ability of an aquifer to retard the groundwater transport of toxic or radioactive ions can be inferred from the analysis of groundwater for the radionuclides of the 238U- and 232Th-decay chains. Groundwaters of varying chemical composition were analyzed from wells in Long Island, New York, and Connecticut. Aquifer lithologies are arkose, quartz sandstone, granite, and glacial drift. Adsorption ( k1) and desorption ( k2) coefficients for Ra and Pb were calculated using 222Rn activity as a measure of the supply of other α-recoil nuclides. Laboratory tests of the validity of this assumption were made by measuring the flux of 224Ra and 222Rn from aquifer solids. The ratio k 1/k 2 is the distribution coefficient, K, which is effectively equal to R ƒ, the retardation factor. The average value of K for Ra is 6 × 10 2 in Long Island aquifers and 5 × 10 4 in Connecticut. The distribution coefficient for Pb is 10 4 in Long Island and 10 5 in Connecticut. Results from this and other studies reveal a strong dependence of retardation on pH, ƒ O 2, and ionic strength that tends to overwhelm any dependence of retardation on lithology.

  17. Prompt fission neutron spectra in fast-neutron-induced fission of 238U

    NASA Astrophysics Data System (ADS)

    Desai, V. V.; Nayak, B. K.; Saxena, A.; Suryanarayana, S. V.; Capote, R.

    2015-07-01

    Prompt fission neutron spectrum (PFNS) measurements for the neutron-induced fission of 238U are carried out at incident neutron energies of 2.0, 2.5, and 3.0 MeV, respectively. The time-of-flight technique is employed to determine the energy of fission neutrons. The prompt fission neutron energy spectra so obtained are analyzed using Watt parametrization to derive the neutron multiplicity and average prompt fission neutron energy. The present experimental PFNS data are compared with the evaluated spectra taken from the ENDF/B-VII.1 library and the predictive calculations carried out using the empire-3.2 (Malta) code with built-in Los Alamos (LA) and Kornilov PFNS models. The sensitivity of the empire-3.2 LA model-calculated PFNS to the nuclear level density parameter of the average fission fragment and to the total kinetic energy is investigated. empire-3.2 LA model PFNS calculations that use Madland 2006-recommended values [D. G. Madland, Nucl. Phys. A 772, 113 (2006), 10.1016/j.nuclphysa.2006.03.013] of the total kinetic energy and the level density parameter a =A /(10 ±0.5 ) compare very well to measured data at all incident neutron incident energies.

  18. Potential Human Health Risk by Metal(loid)s, 234,238U and 210Po due to Consumption of Fish from the “Luis L. Leon” Reservoir (Northern México)

    PubMed Central

    Luna-Porres, Mayra Y.; Rodríguez-Villa, Marco A.; Herrera-Peraza, Eduardo F.; Renteria-Villalobos, Marusia; Montero-Cabrera, María E.

    2014-01-01

    Concentrations of As, Cu, Fe, Hg, Pb and Zn and activity concentrations from 234,238U and 210Po in water, fillet, liver and gills were determined in three stocked fish species from the Luis L. Leon reservoir, located in Northern Mexico. The considered species were Lepomis cyanellus, Cyprinus carpio and Ictalurus furcatus. 238U and 234U activity concentration (AC) in fillet samples showed values of 0.007–0.014 and 0.01–0.02 Bq∙kg−1 wet weight (ww), respectively. Liver samples for L. cyanellus, C. carpio and I. furcatus present 210Po AC of 1.16–3.26, 0.70–1.13 and 0.93–1.37 Bq∙kg−1 ww. Arsenic, mercury and lead concentration intervals in fillet samples were 0.13–0.39, 0.005–0.126 and 0.009–0.08 mg∙kg−1 ww, respectively, while in gill samples they were 0.11–0.43, 0.002–0.039 and 0.02–0.26 mg∙kg−1 ww. The elemental Bioaccumulation Factor (BAF) for fish tissues with respect to their concentrations in water was determined. L. cyanellus showed the highest BAF values for As and total U, being BAFAs = 37 and 40 L∙kg−1 in fillet and gills, respectively, and BAFU total = 1.5 L∙kg−1 in fillet. I. furcatus showed the highest BAF values for Hg and Pb, being BAFHg = 40 and 13 L∙kg−1 in fillet and gills, and BAFPb = 6.5 and 22 L∙kg−1 in fillet and gills, respectively. Some metal(loid) concentrations are slightly higher than European regulations for fish fillets. The difference in concentrations of metal(loid)s in fillet among the studied species is probably due to their differences in diet and habitat. PMID:24968208

  19. A modern framework for the interpretation of 238U/235U in studies of ancient ocean redox

    NASA Astrophysics Data System (ADS)

    Andersen, M. B.; Romaniello, S.; Vance, D.; Little, S. H.; Herdman, R.; Lyons, T. W.

    2014-08-01

    The abundance and isotope composition of redox sensitive elements in ancient sediments are increasingly used to understand the past ocean's geochemical state and the oxygenation history of the Earth. The redox transition of uranium (U) from soluble U+6 to relatively insoluble U+4 and its subsequent incorporation into reduced sediments has been used to deduce the redox state of the oceans in the past. Furthermore, recent analytical improvements have revealed significant 238U/235U fractionation during this redox transition, offering the potential for U isotopes to act as a redox proxy. However, the development of U isotopes as a geochemical tracer requires that U isotope systematics associated with redox changes, are well-characterized. This study focuses on U isotopes in recent sediments from the two largest modern anoxic ocean basins, the Black Sea and the Cariaco Basin, with the aim of advancing our understanding of the U isotope systematics in reducing marine environments. These anoxic sediments have high U accumulation rates and high 238U/235U ratios relative to seawater, in general agreement with a process that accumulates reduced U with a heavy isotopic composition. Using Al and Ca concentrations to correct for detrital and biogenic carbonate-bound U, we estimate the reduced authigenic U accumulated in the sediments and its 238U/235U. These results highlight the importance of isotopic mass balance constraints during diffusive transport and reaction of U from seawater and through pore-water, affecting the observed 238U/235U in sediments. Using these constraints, the average percentages of U depletion from top to bottom of the water column can be estimated, assuming batch-removal of U into anoxic sediments in a restricted basin. Using this framework, 238U/235U in modern anoxic sediments from the Black Sea imply U depletions in the water column of ∼30%, which is close to the observed ∼40% U depletion in the modern Black Sea water column at these depths

  20. Light and heavy transfer products in 136Xe+238U multinucleon transfer reactions

    NASA Astrophysics Data System (ADS)

    Vogt, A.; Birkenbach, B.; Reiter, P.; Corradi, L.; Mijatović, T.; Montanari, D.; Szilner, S.; Bazzacco, D.; Bowry, M.; Bracco, A.; Bruyneel, B.; Crespi, F. C. L.; de Angelis, G.; Désesquelles, P.; Eberth, J.; Farnea, E.; Fioretto, E.; Gadea, A.; Geibel, K.; Gengelbach, A.; Giaz, A.; Görgen, A.; Gottardo, A.; Grebosz, J.; Hess, H.; John, P. R.; Jolie, J.; Judson, D. S.; Jungclaus, A.; Korten, W.; Leoni, S.; Lunardi, S.; Menegazzo, R.; Mengoni, D.; Michelagnoli, C.; Montagnoli, G.; Napoli, D.; Pellegri, L.; Pollarolo, G.; Pullia, A.; Quintana, B.; Radeck, F.; Recchia, F.; Rosso, D.; Şahin, E.; Salsac, M. D.; Scarlassara, F.; Söderström, P.-A.; Stefanini, A. M.; Steinbach, T.; Stezowski, O.; Szpak, B.; Theisen, Ch.; Ur, C.; Valiente-Dobón, J. J.; Vandone, V.; Wiens, A.

    2015-08-01

    Background: Multinucleon transfer reactions (MNT) are a competitive tool to populate exotic neutron-rich nuclei in a wide region of nuclei, where other production methods have severe limitations or cannot be used at all. Purpose: Experimental information on the yields of MNT reactions in comparison with theoretical calculations are necessary to make predictions for the production of neutron-rich heavy nuclei. It is crucial to determine the fraction of MNT reaction products which are surviving neutron emission or fission at the high excitation energy after the nucleon exchange. Method: Multinucleon transfer reactions in +238U 136Xe have been measured in a high-resolution γ -ray/particle coincidence experiment. The large solid-angle magnetic spectrometer PRISMA coupled to the high-resolution Advanced Gamma Tracking Array (AGATA) has been employed. Beamlike reaction products after multinucleon transfer in the Xe region were identified and selected with the PRISMA spectrometer. Coincident particles were tagged by multichannel plate detectors placed at the grazing angle of the targetlike recoils inside the scattering chamber. Results: Mass yields have been extracted and compared with calculations based on the grazing model for MNT reactions. Kinematic coincidences between the binary reaction products, i.e., beamlike and targetlike nuclei, were exploited to obtain population yields for nuclei in the actinide region and compared to x-ray yields measured by AGATA. Conclusions: No sizable yield of actinide nuclei beyond Z =93 is found to perform nuclear structure investigations. In-beam γ -ray spectroscopy is feasible for few-neutron transfer channels in U and the -2 p channel populating Th isotopes.

  1. Investigation of (235)U, (226)Ra, (232)Th, (40)K, (137)Cs, and heavy metal concentrations in Anzali international wetland using high-resolution gamma-ray spectrometry and atomic absorption spectroscopy.

    PubMed

    Zare, Mohammad Reza; Kamali, Mahdi; Fallahi Kapourchali, Maryam; Bagheri, Hashem; Khoram Bagheri, Mahdi; Abedini, Ali; Pakzad, Hamid Reza

    2016-02-01

    Measurements of natural radioactivity levels and heavy metals in sediment and soil samples of the Anzali international wetland were carried out by two HPGe-gamma ray spectrometry and atomic absorption spectroscopy techniques. The concentrations of (235)U, (226)Ra, (232)Th, (40)K, and (137)Cs in sediment samples ranged between 1.05 ± 0.51-5.81 ± 0.61, 18.06 ± 0.63-33.36 ± .0.34, 17.57 ± 0.38-45.84 ± 6.23, 371.88 ± 6.36-652.28 ± 11.60, and 0.43 ± 0.06-63.35 ± 0.94 Bq/kg, while in the soil samples they vary between 2.36-5.97, 22.71-38.37, 29.27-42.89, 472.66-533, and 1.05-9.60 Bq/kg for (235)U, (226)Ra, (232)Th, (40)K, and (137)Cs, respectively. Present results are compared with the available literature data and also with the world average values. The radium equivalent activity was well below the defined limit of 370 Bq/kg. The external hazard indices were found to be less than 1, indicating a low dose. Heavy metal concentrations were found to decrease in order as Fe > Mn > Sr > Zn > Cu > Cr > Ni > Pb > Co > Cd. These measurements will serve as background reference levels for the Anzali wetland.

  2. Absolute L X-ray intensities in the decays of 230Th, 234U, 238Pu and 244Cm

    NASA Astrophysics Data System (ADS)

    Johnston, Peter N.; Burns, Peter A.

    1995-02-01

    The absolute L X-ray emission rates of 230Th, 234U, 238Pu and 244Cm have been measured. The rates were obtained by an alpha-particle gated photon spectrometry technique involving the use of a highly calibrated Ge(HP) detector in coincidence with a SiSB detector. The directional correlation between L X-rays and alpha-particles has been accounted for. The present results are compared with previous experimental values and theoretical estimates. Agreement with theoretical estimates is good, however few of the previous experimental values agree with the present work. Differences with previous work partly seem to lie with the detector calibration.

  3. Counting neutrons from the spontaneous fission of {sup 238}U using scintillation detectors and mixed field analysers

    SciTech Connect

    Parker, Helen M. O'D.; Joyce, Malcolm J.; Jones, Ashley

    2015-07-01

    It is well documented that {sup 238}U decays by spontaneous fission, and that it is the main component of most nuclear fuels. As nuclear fuels are largely classed as Special Nuclear Material (SNM), they have to be fully accounted for by owners and processing facilities. One possible method for verifying declared amounts of SNM is to count the spontaneous neutrons produced from {sup 238}U. Using four EJ-309 liquid scintillation detectors and a mixed field analyser, spontaneous neutrons from 16.4 g of depleted uranium (0.3% enrichment) have been assayed. The assay method shows promising results and this proof of principle will be researched further in order for it to be applied in an industrial setting. (authors)

  4. Comparison of yields of neutron-rich nuclei in proton- and photon-induced 238U fission

    NASA Astrophysics Data System (ADS)

    Khan, F. A.; Bhowmick, Debasis; Basu, D. N.; Farooq, M.; Chakrabarti, Alok

    2016-11-01

    A comparative study of fission of actinides, especially 238U, by proton and bremsstrahlung photon is performed. The relative mass distribution of 238U fission fragments has been explored theoretically for both proton- and photon-induced fission. The integrated yield along with charge distribution of the products are calculated to find the neutron richness in comparison with the nuclei produced by the r process in nucleosynthesis. Some r -process nuclei in the intermediate-mass range for symmetric fission mode are found to be produced almost two orders of magnitude more for proton-induced fission than for photofission, although the rest of the neutron-rich nuclei in the asymmetric mode are produced in comparable proportion for both processes.

  5. Light nuclides produced in the proton-induced spallation of {sup 238}U at 1 GeV

    SciTech Connect

    Ricciardi, M.V.; Armbruster, P.; Enqvist, T.; Kelic, A.; Rejmund, F.; Schmidt, K.-H.; Yordanov, O.; Benlliure, J.; Pereira, J.; Bernas, M.; Mustapha, B.; Stephan, C.; Tassan-Got, L.

    2006-01-15

    The production of light and intermediate-mass nuclides formed in the reaction {sup 1}H+{sup 238}U at 1 GeV was measured at the Fragment Separator at GSI, Darmstadt. The experiment was performed in inverse kinematics, by shooting a 1 A GeV {sup 238}U beam on a thin liquid-hydrogen target. A total of 254 isotopes of all elements in the range 7{<=}Z{<=}37 were unambiguously identified, and the velocity distributions of the produced nuclides were determined with high precision. The results show that the nuclides are produced in a very asymmetric binary decay of heavy nuclei originating from the spallation of uranium. All the features of the produced nuclides merge with the characteristics of the fission products as their mass increases.

  6. Giant resonances in {sup 238}U within the quasiparticle random-phase approximation with the Gogny force

    SciTech Connect

    Peru, S.; Gosselin, G.; Martini, M.; Dupuis, M.; Hilaire, S.

    2011-01-15

    Fully consistent axially-symmetric deformed quasiparticle random-phase approximation (QRPA) calculations have been performed, using the same Gogny D1S effective force for both the Hartree-Fock-Bogolyubov mean field and QRPA matrix. New implementation of this approach leads to the applicability of QRPA to heavy deformed nuclei. Giant resonances and low-energy collective states for monopole, dipole, quadrupole, and octupole modes are predicted for the heavy deformed nucleus {sup 238}U and compared with experimental data.

  7. Solubility of {sup 238}U radionuclide from various types of soil in synthetic gastrointestinal fluids using “US in vitro” digestion method

    SciTech Connect

    Rashid, Nur Shahidah Abdul; Sarmani, Sukiman; Majid, Amran Ab.; Mohamed, Faizal; Siong, Khoo Kok

    2015-04-29

    238U radionuclide is a naturally occuring radioactive material that can be found in soil. In this study, the solubility of 238U radionuclide obtained from various types of soil in synthetic gastrointestinal fluids was analysed by “US P in vitro” digestion method. The synthetic gastrointestinal fluids were added to the samples with well-ordered, mixed throughly and incubated according to the human physiology digestive system. The concentration of 238U radionuclide in the solutions extracted from the soil was measured using Induced Coupling Plasma Mass Spectrometer (ICP-MS). The concentration of 238U radionuclide from the soil samples in synthetic gastrointestinal fluids showed different values due to different homogenity of soil types and chemical reaction of 238U radionuclide. In general, the solubility of 238U radionuclide in gastric fluid was higher (0.050 – 0.209 ppm) than gastrointestinal fluids (0.024 – 0.050 ppm). It could be concluded that the US P in vitro digestion method is practicle for estimating the solubility of 238U radionuclide from soil materials and could be useful for monitoring and risk assessment purposes applying to environmental, health and contaminated soil samples.

  8. Measurement of evaporation residue cross-sections of the reaction 30Si + 238U at subbarrier energies

    SciTech Connect

    Nishio, K.; Ikezoe, H.; Mitsuoka, S.; Nagame, Y.; Tsukada, K.; Tsuruta, K.; Hofmann, S.; Hessberger, F. P.; Ackermann, D.; Heinz, S.; Khuyagbaatar, J.; Kindler, B.; Kojouharov, I.; Lommel, B.; Mazzocco, M.; Schoett, H. J.; Antalic, S.; Saro, S.; Comas, V. F.; Heredia, J. A.

    2007-02-26

    The reaction 30Si + 238U {yields} 268Sg* was studied at beam energies close to the Coulomb barrier. At the above barrier energy of Ec.m. = 144.0 MeV (center-of-mass energy at half thickness of the target), we measured three decay chains of 263Sg produced by evaporation of five neutrons. The cross-section was (67{sub -37}{sup +67}) pb. At subbarrier energy of Ec.m. = 133.0 MeV we measured three spontaneously fissioning nuclei which we assigned to the isotope 264Sg. The half-life of (120{sub -44}{sup +126}) ms was determined. The production cross-section was (10{sub -6}{sup +10}) pb, which is about four orders magnitude larger than the calculation based on the one-dimensional barrier penetration model in the fusion process, showing fusion enhancement caused by the prolate deformation of 238U. At Ec.m. = 128.0 MeV an upper cross-section limit of 15 pb was measured. Compared to excitation functions measured for the lighter system 16O + 238U {yields} 254Fm*, a reduction of the fusion probability was observed at low beam energies indicating increasing competition from quasifission processes.

  9. Investigation of the 238U(d ,p ) surrogate reaction via the simultaneous measurement of γ -decay and fission probabilities

    NASA Astrophysics Data System (ADS)

    Ducasse, Q.; Jurado, B.; Aïche, M.; Marini, P.; Mathieu, L.; Görgen, A.; Guttormsen, M.; Larsen, A. C.; Tornyi, T.; Wilson, J. N.; Barreau, G.; Boutoux, G.; Czajkowski, S.; Giacoppo, F.; Gunsing, F.; Hagen, T. W.; Lebois, M.; Lei, J.; Méot, V.; Morillon, B.; Moro, A. M.; Renstrøm, T.; Roig, O.; Rose, S. J.; Sérot, O.; Siem, S.; Tsekhanovich, I.; Tveten, G. M.; Wiedeking, M.

    2016-08-01

    We investigated the 238U(d ,p ) reaction as a surrogate for the n +238U reaction. For this purpose we measured for the first time the γ -decay and fission probabilities of *239U simultaneously and compared them to the corresponding neutron-induced data. We present the details of the procedure to infer the decay probabilities, as well as a thorough uncertainty analysis, including parameter correlations. Calculations based on the continuum-discretized coupled-channels method and the distorted-wave Born approximation (DWBA) were used to correct our data from detected protons originating from elastic and inelastic deuteron breakup. In the region where fission and γ emission compete, the corrected fission probability is in agreement with neutron-induced data, whereas the γ -decay probability is much higher than the neutron-induced data. We have performed calculations of the decay probabilities with the statistical model and of the average angular momentum populated in the 238U(d ,p ) reaction with the DWBA to interpret these results.

  10. Actinides produced by /sup 12/C + /sup 242/Pu and /sup 16/O + /sup 238/U reactions

    SciTech Connect

    Shinohara, N.; Usuda, S.; Ichikawa, S.; Suzuki, T.; Magara, M.; Okashita, H.; Yoshikawa, H.; Horiguchi, T.; Iwata, Y.; Shibata, S.; and others

    1986-09-01

    The cross sections for /sup 250/Fm, /sup 244-246/Cf, /sup 242-244/Cm, and /sup 242/Am/sup g-italic/ produced by the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions leading to the same compound nucleus of /sup 254/Fm have been measured by using radiochemical methods. The excitation functions show that the difference between the /sup 12/C+ /sup 242/Pu and the /sup 16/O+ /sup 238/U reactions can be attributed mainly to the Coulomb barriers. Our results were compared with others reported previously for /sup 22/Ne+ /sup 232/Th, /sup 12/C+ /sup 238/U, /sup 12/C+ /sup 240,241/Pu, /sup 13/C+ /sup 241/Pu, /sup 16/O+ /sup 233/U, and /sup 16/O+ /sup 242/Pu reaction systems, and support a mechanism involving transfer of ..cap alpha..-particle clusters (C,Be,He) from projectile to target for the production of Cf and Cm isotopes.

  11. Uranium ((238)U)-induced ROS and cell cycle perturbations, antioxidant responses and erythrocyte nuclear abnormalities in the freshwater iridescent shark fish Pangasius sutchi.

    PubMed

    Annamalai, Sathesh Kumar; Arunachalam, Kantha Deivi

    2017-03-02

    The strategic plan of this study is to analyze any possible radiological impact on aquatic organisms from forthcoming uranium mining facilities around the Nagarjuna Sagar Dam in the future. The predominantly consumed and dominant fish species Pangasius sutchi, which is available year-round at Nagarjuna Sagar Dam, was selected for the study. To comprehend the outcome and to understand the mode of action of (238)U, the fish species Pangasius sutchi was exposed to ¼ and ½ of the LC50 doses of waterborne (238)U in a static system in duplicate for 21 days. Blood and organs, including the gills, liver, brain and muscles, were collected at different time periods-0h, 24h, 48h, 72h, 96h, 7, days 14days and 21 days-using ICP-MS to determine the toxic effects of uranium and the accumulation of (238)U concentrations. The bioaccumulation of (238)U in P. sutchi tissues was dependent on exposure time and concentration. The accumulation of uranium was, in order of magnitude, measured as gills>liver>brain>tissue, with the highest accumulation in the gills. It was observed that exposure to (238)U significantly reduced antioxidant enzymes such as superoxide dismutase, catalase, and lipid peroxidase. The analysis of DNA fragmentation by comet assay and cell viability by flow cytometry was performed at different time intervals. DNA histograms by flow cytometry analysis revealed an increase in the G2/M phase and the S phase. The long-term (238)U exposure studies in fish showed increasing micronucleus frequencies in erythrocytes with greater exposure time. The higher the concentration of (238)U is, the greater is the effect observed, suggesting a close relationship between accumulation and toxicity. A possible ROS-mediated (238)U toxicity mechanism and antioxidant responses have been proposed.

  12. Analysis and comparison of monoenergetic fast neutron fluence determination using 238U samples at different positions with respect to the neutron source.

    PubMed

    Zhang, Guohui; Liu, Xiang; Gao, Zhiqi; Wu, Hao; Liu, Jiaming

    2012-05-01

    Using two (238)U samples placed in a gridded ionization chamber and a parallel-plate fission chamber, fluence of monoenergetic fast neutrons was determined. Four runs of measurements were performed. Analysis showed that although the neutron fluences for the two (238)U samples differ by 20-33 times in the present work, the fluences at the position of the sample in the gridded ionization chamber determined by the two ways are in agreement within experimental uncertainties.

  13. Uranium-series disequilibrium in tuffs from Yucca Mountain, Nevada, as evidence of pore-fluid flow over the last million years

    USGS Publications Warehouse

    Gascoyne, M.; Miller, N.H.; Neymark, L.A.

    2002-01-01

    Samples of tuff from boreholes drilled into fault zones in the Exploratory Studies Facility (ESF) and relatively unfractured rock of the Cross Drift tunnels, at Yucca Mountain, Nevada, have been analysed by U-series methods. This work is part of a project to verify the finding of fast flow-paths through the tuff to ESF level, indicated by the presence of 'bomb' 36Cl in pore fluids. Secular radioactive equilibrium in the U decay series, (i.e. when the radioactivity ratios 234U/238U, 230Th/234U and 226Ra/230Th all equal 1.00) might be expected if the tuff samples have not experienced radionuclide loss due to rock-water interaction occurring within the last million years. However, most fractured and unfractured samples were found to have a small deficiency of 234U (weighted mean 234U/238U=0.95??0.01) and a small excess of 230Th (weighted mean 230Th/234U 1.10??0.02). The 226Ra/230Th ratios are close to secular equilibrium (weighted mean = 0.94??0.07). These data indicate that 234U has been removed from the rock samples in the last ???350 ka, probably by pore fluids. Within the precision of the measurement, it would appear that 226Ra has not been mobilized and removed from the tuff, although there may be some localised 226Ra redistribution as suggested by a few ratio values that are significantly different from 1.0. Because both fractured and unfractured tuffs show approximately the same deficiency of 234U, this indicates that pore fluids are moving equally through fractured and unfractured rock, More importantly, fractured rock appears not to be a dominant pathway for groundwater flow (otherwise the ratio would be more strongly affected and the Th and Ra isotopic ratios would likely also show disequilibrium). Application of a simple mass-balance model suggests that surface infiltration rate is over an order of magnitude greater than the rate indicated by other infiltration models and that residence time of pore fluids at ESF level is about 400 a. Processes of U

  14. 238U-230Th dating of chevkinite in high-silica rhyolites from La Primavera and Yellowstone calderas

    USGS Publications Warehouse

    Vazquez, Jorge A.; Velasco, Noel O.; Schmitt, Axel K.; Bleick, Heather A.; Stelten, Mark E.

    2014-01-01

    Application of 238U-230Th disequilibrium dating of accessory minerals with contrasting stabilities and compositions can provide a unique perspective on magmatic evolution by placing the thermochemical evolution of magma within the framework of absolute time. Chevkinite, a Th-rich accessory mineral that occurs in peralkaline and metaluminous rhyolites, may be particularly useful as a chronometer of crystallization and differentiation because its composition may reflect the chemical changes of its host melt. Ion microprobe 128U-230Th dating of single chevkinite microphenocrysts from pre- and post-caldera La Primavera, Mexico, rhyolites yields model crystallization ages that are within 10's of k.y. of their corresponding K-Ar ages of ca. 125 ka to 85 ka, while chevkinite microphenocrysts from a post-caldera Yellowstone, USA, rhyolite yield a range of ages from ca. 110 ka to 250 ka, which is indistinguishable from the age distribution of coexisting zircon. Internal chevkinite-zircon isochrons from La Primavera yield Pleistocene ages with ~5% precision due to the nearly two order difference in Th/U between both minerals. Coupling chevkinite 238U-230Th ages and compositional analyses reveals a secular trend of Th/U and rare earth elements recorded in Yellowstone rhyolite, likely reflecting progressive compositional evolution of host magma. The relatively short timescale between chevkinite-zircon crystallization and eruption suggests that crystal-poor rhyolites at La Primavera were erupted shortly after differentiation and/or reheating. These results indicate that 238U-230Th dating of chevkinite via ion microprobe analysis may be used to date crystallization and chemical evolution of silicic magmas.

  15. TECHNICAL EQUIVALENCE BETWEEN PERKIN-ELMER DRCe AND ELAN 6000 FOR THE ANALYSIS OF 238U IN URINE BIOASSAY SAMPLES

    SciTech Connect

    Wong, C T; Collins, L J

    2007-09-05

    The LLNL Bioassay Laboratory recently purchased a Perkin-Elmer DRCe ICP-MS (DRCe) to replace the existing Perkin-Elmer Elan 6000 ICP-MS (Elan 6000) used for the analysis of {sup 238}U in urine bioassay samples. In accordance with section 5.7.2 of DOE-STD-1112-98, 'The Department of Energy Laboratory Accreditation Program for Radiobioassay', this document demonstrates that the DRCe is technically equivalent to the Elan 6000. This paper documents: (1) Minor changes made in the procedure to improve the sensitivity; (2) Detection limits for the Elan 6000 and the DRCe; (3) Determination of the measurement uncertainty for the DRCe; and (4) Comparison of results from the DRCe versus the Elan 6000. A 1 mL aliquot of the sample is transferred to an auto sampler tube. Nitric acid and {sup 233}U (used as an internal standard) are added to the samples and the samples are digested in a microwave oven. The digested samples are diluted to 10 mL with deionized water and the {sup 238}U concentration is determined by ICP-MS. The ICP-MS is calibrated with a series of {sup 238}U standards. {sup 233}U is used as an internal standard to correct for suppression of the signal due to the sample matrix. The Elan 6000 is run in the peakhopping mode with 100 ms dwell times and 50 sweeps. The total integration time is 5,000 ms. The average of two measurements is used for the determination.

  16. Determination of natural radioactivity in irrigation water of drilled wells in northwestern Saudi Arabia.

    PubMed

    Alkhomashi, N; Al-Hamarneh, Ibrahim F; Almasoud, Fahad I

    2016-02-01

    The levels of natural radiation in bedrock groundwater extracted from drilled wells in selected farms in the northwestern part of Saudi Arabia were addressed. The investigated waters form a source of irrigation for vegetables, agricultural crops, wheat, and alfalfa to feed livestock consumed by the general public. Information about water radioactivity in this area is not available yet. Therefore, this study strives to contribute to the quality assessment of the groundwater of these wells that are drilled into the non-renewable Saq sandstone aquifer. Hence, gross alpha and beta activities as well as the concentrations of (224)Ra, (226)Ra, (228)Ra, (234)U, (238)U, and U(total) were measured, compared to national and international limits and contrasted with data quoted from the literature. Correlations between the activities of the analyzed radionuclides were discussed. The concentrations of gross alpha and beta activities as well as (228)Ra were identified by liquid scintillation counting whereas alpha spectrometry was used to determine (224)Ra, (226)Ra, (234)U and (238)U after separation from the matrix by extraction chromatography. The mean activity concentrations of gross α and β were 3.15 ± 0.26 Bq L(-1) and 5.39 ± 0.44 Bq L(-1), respectively. Radium isotopes ((228)Ra and (226)Ra) showed mean concentrations of 3.16 ± 0.17 Bq L(-1) and 1.12 ± 0.07 Bq L(-1), respectively, whereas lower levels of uranium isotopes ((234)U and (238)U) were obtained.

  17. Neutron multiplicity in the fission of 238U and 235U with neutrons up to 200 MeV.

    PubMed

    Ethvignot, T; Devlin, M; Duarte, H; Granier, T; Haight, R C; Morillon, B; Nelson, R O; O'Donnell, J M; Rochman, D

    2005-02-11

    Prompt-fission-neutron multiplicities were measured for 238U(n,f) and 235U(n,f) from 0.4 to 200 MeV. The data are of great importance in connection with accelerator-coupled nuclear reactor systems incinerating actinides. We report that fission induced by 200 MeV neutrons produces approximately 10 more prompt neutrons than fission induced by reactor neutrons. Most neutrons are evaporated from the fission fragments and the prefission compound nucleus, as the preequilibrium emission of energetic neutrons accounts for a maximum of 15% of the prompt neutrons at 200 MeV.

  18. Neutron-deficient N{approx_equal}126 nuclei produced in 238U fragmentation: population of high-spin states

    SciTech Connect

    Podolyak, Zs.; Regan, P. H.; Walker, P. M.; Pearson, C. J.; Valiente-Dobon, J. J.; Gerl, J.; Hellstroem, M.; Becker, F.; Gorska, M.; Kelic, A.; Kopatch, Y.; Mandal, S.; Schmidt, K.-H.; Wollersheim, H. J.; Banu, A.; Geissel, H.; Grawe, H.; Kojouharov, I.; Lozeva, R.; Portillo, M.

    2006-04-26

    The population of metastable states produced in relativistic-energy fragmentation of a 238U beam has been measured. For states with high angular momentum, I=17({Dirac_h}/2{pi}) and I=21.5({Dirac_h}/2{pi}), a higher population than expected has been observed, with the discrepancy increasing with angular momentum. By considering two sources for the angular momentum, related to single-particle and collective motions, a much improved description of the experimental results can be obtained. In addition, new results on the structure of 208Fr, 211Ra and 216Ac are reported.

  19. U-Th-Ra disequilibria in sediments of the Dora Baltea river (Italia)

    NASA Astrophysics Data System (ADS)

    Chabaux, F.; Deloche, A.; Pelt, E.; Granet, M.; Perrone, Th.; Boutin, R.; Viville, D.; Rihs, S.; Stille, P.

    2012-04-01

    In order to constrain the transfer time of sediments in Alpine rivers, we propose to use the U-series nuclides approach recently developed for Himalayan rivers (e.g., Chabaux et al., 2008; Granet et al., 2010). Therefore, a series of bank sediments has beeen collected along the Dora Baltea river (Italia), one of the Po's tributaries draining the southern slope of the Mont Blanc Massif. In addition to U series nuclides, major and trace element concentrations and Sr and Nd isotope ratios have been analyzed for each sample. The study indicates that the (234U/238U)-, (230Th/234U)- and the (226Ra/230Th)- activity ratios are very similar for all the samples, whereas the 230Th/232Th ratios can differ from one sample to another. Such a variation, consistent with the Sr and Nd isotope data, is certainly the consequence of mineralogical heterogeneities in the samples. This suggests that the use of 238U-230Th-232Th systematics alone is probably insufficient for constraining the transfer time of sediments in the Po rivers alluvial plain, whereas the combination of 238U-230Th disequilibrium with the 230Th-226Ra disequilibrium can help to constrain such time information.

  20. Uranium series isotopes concentration in sediments at San Marcos and Luis L. Leon reservoirs, Chihuahua, Mexico

    NASA Astrophysics Data System (ADS)

    Méndez-García, C.; Renteria-Villalobos, M.; García-Tenorio, R.; Montero-Cabrera, M. E.

    2014-07-01

    Spatial and temporal distribution of the radioisotopes concentrations were determined in sediments near the surface and core samples extracted from two reservoirs located in an arid region close to Chihuahua City, Mexico. At San Marcos reservoir one core was studied, while from Luis L. Leon reservoir one core from the entrance and another one close to the wall were investigated. 232Th-series, 238U-series, 40K and 137Cs activity concentrations (AC, Bq kg-1) were determined by gamma spectrometry with a high purity Ge detector. 238U and 234U ACs were obtained by liquid scintillation and alpha spectrometry with a surface barrier detector. Dating of core sediments was performed applying CRS method to 210Pb activities. Results were verified by 137Cs AC. Resulting activity concentrations were compared among corresponding surface and core sediments. High 238U-series AC values were found in sediments from San Marcos reservoir, because this site is located close to the Victorino uranium deposit. Low AC values found in Luis L. Leon reservoir suggest that the uranium present in the source of the Sacramento - Chuviscar Rivers is not transported up to the Conchos River. Activity ratios (AR) 234U/overflow="scroll">238U and 238U/overflow="scroll">226Ra in sediments have values between 0.9-1.2, showing a behavior close to radioactive equilibrium in the entire basin. 232Th/overflow="scroll">238U, 228Ra/overflow="scroll">226Ra ARs are witnesses of the different geological origin of sediments from San Marcos and Luis L. Leon reservoirs.

  1. Primordial radioactivity ((238)U, (232)Th and (40)K) measurements for soils of Ludhiana district of Punjab, India.

    PubMed

    Badhan, K; Mehra, R

    2012-11-01

    The aim of the present work was to study the activity concentration and absorbed gamma dose rates due to primordial radionuclides ((238)U, (232)Th and (40)K) for the soil of different villages of Ludhiana district of Punjab, India using a high-purity germanium detector based on high resolution gamma-ray spectrometry. The average activity concentrations of (238)U, (232)Th and (40)K in the soil samples have been found to be 28.58, 50.95 and 569.59 Bq kg(-1), respectively, which gives the total gamma dose rate contribution of 68.50 nGy h(-1). To evaluate the radiological hazard of the natural radioactivity, the radium equivalent activity, the external hazard index, the absorbed dose rate and the effective dose rate have been calculated. The calculated radium equivalent activity values are on the lower side of the recommended safe limit value of 370 Bq kg(-1) by Organization of Economic and Control Department. The calculated value of external health hazard index is lower than unity.

  2. Fission Fragment Angular Distribution measurements of 235U and 238U at CERN n_TOF facility

    NASA Astrophysics Data System (ADS)

    Leal-Cidoncha, E.; Durán, I.; Paradela, C.; Tarrío, D.; Leong, L. S.; Tassan-Got, L.; Audouin, L.; Altstadt, S.; Andrzejewski, J.; Barbagallo, M.; Bécares, V.; Bečvář, F.; Belloni, F.; Berthoumieux, E.; Billowes, J.; Boccone, V.; Bosnar, D.; Brugger, M.; Calviani, M.; Calviño, F.; Cano-Ott, D.; Carrapiço, C.; Cerutti, F.; Chiaveri, E.; Chin, M.; Colonna, N.; Cortés, G.; Cortés-Giraldo, M. A.; Diakaki, M.; Domingo-Pardo, C.; Dressler, R.; Dzysiuk, N.; Eleftheriadis, C.; Ferrari, A.; Fraval, K.; Ganesan, S.; García, A. R.; Giubrone, G.; Gómez-Hornillos, M. B.; Gonçalves, I. F.; González-Romero, E.; Griesmayer, E.; Guerrero, C.; Gunsing, F.; Gurusamy, P.; Hernández-Prieto, A.; Jenkins, D. G.; Jericha, E.; Kadi, Y.; Käppeler, F.; Karadimos, D.; Kivel, N.; Koehler, P.; Kokkoris, M.; Krtička, M.; Kroll, J.; Lampoudis, C.; Langer, C.; Lederer, C.; Leeb, H.; Lo Meo, S.; Losito, R.; Mallick, A.; Manousos, A.; Marganiec, J.; Martínez, T.; Massimi, C.; Mastinu, P. F.; Mastromarco, M.; Meaze, M.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mingrone, F.; Mirea, M.; Mondelaers, W.; Pavlik, A.; Perkowski, J.; Plompen, A.; Praena, J.; Quesada, J. M.; Rauscher, T.; Reifarth, R.; Riego, A.; Robles, M. S.; Roman, F.; Rubbia, C.; Sabaté-Gilarte, M.; Sarmento, R.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Tagliente, G.; Tain, J. L.; Tsinganis, A.; Valenta, S.; Vannini, G.; Variale, V.; Vaz, P.; Ventura, A.; Versaci, R.; Vermeulen, M. J.; Vlachoudis, V.; Vlastou, R.; Wallner, A.; Ware, T.; Weigand, M.; Weiß, C.; Wright, T.; Žugec, P.

    2016-03-01

    Neutron-induced fission cross sections of 238U and 235U are used as standards in the fast neutron region up to 200 MeV. A high accuracy of the standards is relevant to experimentally determine other neutron reaction cross sections. Therefore, the detection effciency should be corrected by using the angular distribution of the fission fragments (FFAD), which are barely known above 20 MeV. In addition, the angular distribution of the fragments produced in the fission of highly excited and deformed nuclei is an important observable to investigate the nuclear fission process. In order to measure the FFAD of neutron-induced reactions, a fission detection setup based on parallel-plate avalanche counters (PPACs) has been developed and successfully used at the CERN-n_TOF facility. In this work, we present the preliminary results on the analysis of new 235U(n,f) and 238U(n,f) data in the extended energy range up to 200 MeV compared to the existing experimental data.

  3. Mass Yields and Average Total Kinetic Energy Release in Fission for 235U, 238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Duke, Dana

    2015-10-01

    Mass yield distributions and average total kinetic energy (TKE) in neutron induced fission of 235U, 238U, and 239Pu targets were measured with a gridded ionization chamber. Despite decades of fission research, our understanding of how fragment mass yields and TKE depend on incident neutron energy is limited, especially at higher energies (above 5-10 MeV). Improved accuracy in these quantities is important for nuclear technology as it enhances our simulation capabilities and increases the confidence in diagnostic tools. The data can also guide and validate theoretical fission models where the correlation between the fragment mass and TKE is of particular value for constraining models. The Los Alamos Neutron Science Center - Weapons Neutron Research (LANSCE - WNR) provides a neutron beam with energies from thermal to hundreds of MeV, well-suited for filling in the gaps in existing data and exploring fission behavior in the fast neutron region. The results of the studies on target nuclei 235U, 238U, and 239Pu will be presented with a focus on exploring data trends as a function of neutron energy from thermal through 30 MeV. Results indicate clear evidence of structure due to multi-chance fission in the TKE . LA-UR-15-24761.

  4. A dispersive optical model potential for nucleon induced reactions on 238U and 232Th nuclei with full coupling

    NASA Astrophysics Data System (ADS)

    Quesada, José Manuel; Soukhovitskiĩ, EfremS.; Capote, Roberto; Chiba, Satoshi

    2013-03-01

    A dispersive coupled-channel optical model potential (DCCOMP) that couples the ground-state rotational and low-lying vibrational bands of 238U and 232Th nuclei is studied. The derived DCCOMP couples almost all excited levels below 1 MeV of excitation energy of the corresponding even-even actinides. The ground state, octupole, beta, gamma, and non-axial bands are coupled. The first two isobar analogue states (IAS) populated in the quasi-elastic (p,n) reaction are also coupled in the proton induced calculation, making the potential approximately Lane consistent. The coupled-channel potential is based on a soft-rotor description of the target nucleus structure, where dynamic vibrations are considered as perturbations of the rigid rotor underlying structure. Matrix elements required to use the proposed structure model in Tamura coupled-channel scheme are derived. Calculated ratio R(U238/Th232) of the total cross-section difference to the averaged σT for 238U and 232Th nuclei is shown to be in excellent agreement with measured data.

  5. Spectral interference corrections for the measurement of (238)U in materials rich in thorium by a high resolution gamma-ray spectrometry.

    PubMed

    Yücel, H; Solmaz, A N; Köse, E; Bor, D

    2009-11-01

    In this study, the spectral interferences are investigated for the analytical peaks at 63.3 keV of (234)Th and 1001.0 keV of (234m)Pa, which are often used in the measurement of (238)U activity by the gamma-ray spectrometry. The correction methods are suggested to estimate the net peak areas of the gamma-rays overlapping the analytical peaks, due to the contribution of (232)Th that may not be negligible in materials rich in natural thorium. The activity results for the certified reference materials (CRMs) containing U and Th were measured with a well type Ge detector. The self-absorption and true coincidence-summing (TCS) effects were also taken into account in the measurements. It is found that ignoring the contributions of the interference gamma-rays of (232)Th and (235)U to the mixed peak at 63.3 keV of (234)Th ((238)U) leads to the remarkably large systematic influence of 0.8-122% in the measured (238)U activity, but in case of ignoring the contribution of (232)Th via the interference gamma-ray at 1000.7 keV of (228)Ac to the mixed peak at 1001 keV of (234m)Pa ((238)U) results in relatively smaller systematic influence of 0.05-3%, depending on thorium contents in the samples. The present results showed that the necessary correction for the spectral interferences besides self-absorption and TCS effects is also very important to obtain more accurate (238)U activity results. Additionally, if one ignores the contribution of (232)Th to both (238)U and (40)K activities in materials, the maximum systematic influence on the effective radiation dose is estimated to be ~6% and ~1% via the analytical peaks at 63.3 and 1001 keV for measurement of the (238)U activity, respectively.

  6. Vegetation-derived insights on the mobilization and potential transport of radionuclides from the Nopal I natural analog site, Mexico

    SciTech Connect

    Leslie, B.W.; Pickett, D.A.; Pearcy, E.C.

    1999-07-01

    The Nopal I uranium (U) deposit, Pena Blanca, Mexico is a source term and contaminant transport natural analog to the proposed high-level nuclear waste repository at Yucca Mountain, Nevada. In an attempt to characterize the mobilization and potential transport of radionuclides in the unsaturated zone at the Nopal I deposit, vegetation growing on ore piles was analyzed for {sup 238}U, {sup 235}U, and {sup 232}Th decay-series isotopes. Specimens of Phacelia robusta growing on high-grade piles of U ore were collected and analyzed by alpha autoradiography, and by alpha and gamma spectrometry. Activities for U, thorium (Th), and radium (Ra) isotopes (Bq/kg dried plant) were 300, 1,000, and 7,000 for {sup 238}U, {sup 230}Th, and {sup 226}Ra, respectively. The {sup 226}Ra activities in these specimens are among the highest ever measured for plants; furthermore, the plant-to-soil {sup 226}Ra concentration ratio is higher than expected. These results demonstrate the large mobility and bio-availability of Ra in the Nopal I environment, and support previous indications of recent loss of {sup 226}Ra from the ore body. Comparison between the activities of {sup 238}U and {sup 232}Th decay-chain Th isotopes in the plants and in the ore substrate indicate that relative mobilization into pore solutions of {sup 228}Th > {sup 230}Th > {sup 232}Th, in a ratio of about 50--25:4:1, respectively. The similarity of the plant's {sup 234}U/{sup 238}U activity ratio ({approximately}1.2) to that of a caliche deposit that formed adjacent to the Nopal ore body around 54 ka suggests the {sup 234}U/{sup 238}U activity ratio of U released from the ore is approximately 1.2. The U and {sup 226}Ra isotope activities of the plants and ore substrate, and solubility considerations, are used to assess a source term model of the potential Yucca Mountain repository. These results suggest the use of a natural analog source term model in performance assessments may be non-conservative.

  7. 234U and 230Th determination by FIA-ICP-MS and application to uranium-series disequilibrium in marine samples.

    PubMed

    Godoy, Maria Luiza D P; Godoy, José Marcus; Kowsmann, Renato; Dos Santos, Guaciara M; Petinatti da Cruz, Rosana

    2006-01-01

    A 234U and 230Th determination method based on an extraction chromatographic separation on a flow injection system coupled to a quadruple ICP-MS was developed. Two-milliliter UTEVA (Eichrom Co.) cartridges were applied as separation tool and 236U and 229Th as spikes. Loading and washing steps were carried out in 3 M HNO3 solution and 0.05 M ammonium oxalate applied to elute both uranium and thorium. The method was applied initially to the IAEA-327 soil reference sample and NIST SRM 4357 ocean sediment reference material, with the obtained 234U and 230Th concentrations in agreement with the reference levels. Samples from a deep-sea sediment core (2450 m water depth) were analyzed and based on 230Th/234U dating, a mean sedimentation rate of 3.3 cm ky(-1) was calculated. Samples from two sediment layers were also dated by 14C-AMS and the observed ages agree with the 230Th/234U results.

  8. Trace metal cycling and 238U/235U in New Zealand's fjords: Implications for reconstructing global paleoredox conditions in organic-rich sediments

    NASA Astrophysics Data System (ADS)

    Hinojosa, Jessica L.; Stirling, Claudine H.; Reid, Malcolm R.; Moy, Christopher M.; Wilson, Gary S.

    2016-04-01

    Reconstructing the history of ocean oxygenation provides insight into links between ocean anoxia, biogeochemical cycles, and climate. Certain redox-sensitive elements respond to changes in marine oxygen content through phase shifts and concomitant isotopic fractionation, providing new diagnostic proxies of past ocean hypoxia. Here we explore the behavior and inter-dependence of a suite of commonly utilized redox-sensitive trace metals (U, Mo, Fe, and Mn) and the emerging "stable" isotope system of U (238U/235U, or δ238U) in New Zealand fjords. These semi-restricted basins have chemical conditions spanning the complete redox spectrum from fully oxygenated to suboxic to intermittently anoxic/euxinic. In the anoxic water column, U and Mo concentrations decrease, while Fe and Mn concentrations increase. Similarly, signals of past euxinic conditions can be found by U, Mo, Fe, and Mn enrichment in the underlying sediments. The expected U isotopic shift toward a lower δ238U in the anoxic water column due to U(VI)-U(IV) reduction is not observed; instead, water column δ238U profiles are consistent in fjords of all oxygen content, falling within previously reported ranges for open ocean seawater (δ238U = -0.42 ± 0.07‰). Additionally, surface sediment δ238U results show evidence for competing U isotope fractionation processes. One site indicates increased export of 238U from seawater to the underlying sediments (fractionation between aqueous seawater U and particulate sediment U, or ΔU(aq)-U(solid) = -0.25‰), consistent with redox-driven fractionation. Another site suggests potential U(VI) adsorption-driven fractionation, reflecting increased export of 235U from seawater to sediments (ΔU(aq)-U(solid) = 0.25‰). We discuss several potential factors that could alter δ238U in waters and sediments beyond redox-driven shifts, including adsorption to organic matter in waters of high primary productivity, reaction rates for competing processes of U adsorption and

  9. Towards A Modern Calibration Of The 238U/235U Paleoredox Proxy: Apparent Uranium Isotope Fractionation Factor During U(VI)-U(IV) Reduction In The Black Sea

    NASA Astrophysics Data System (ADS)

    Rolison, J. M.; Stirling, C. H.; Middag, R.; Rijkenberg, M. J. A.; De Baar, H. J. W.

    2015-12-01

    The isotopic compositions of redox-sensitive metals, including uranium (U), in marine sediments have recently emerged as powerful diagnostic tracers of the redox state of the ancient ocean-atmosphere system. Interpretation of sedimentary isotopic information requires a thorough understating of the environmental controls on isotopic fractionation in modern anoxic environments before being applied to the paleo-record. In this study, the relationship between ocean anoxia and the isotopic fractionation of U was investigated in the water column and sediments of the Black Sea. The Black Sea is the world's largest anoxic basin and significant removal of U from the water column and high U accumulation rates in modern underlying sediments have been documented. Removal of U from the water column occurs during the redox transition of soluble U(VI) to relatively insoluble U(IV). The primary results of this study are two-fold. First, significant 238U/235U fractionation was observed in the water column of the Black Sea, suggesting the reduction of U induces 238U/235U fractionation with the preferential removal of 238U from the aqueous phase. Second, the 238U/235U of underlying sediments is related to the water column through the isotope fractionation factor of the reduction reaction but is influenced by mass transport processes. These results provide important constraints on the use of 238U/235U as a proxy of the redox state of ancient oceans.

  10. 238U-Series in Fe Oxy/Hydroxides by LA-MC-ICP-MS, New Insights Into Weathering Geochronology

    NASA Astrophysics Data System (ADS)

    Bernal, J.; McCulloch, M.; Eggins, S.; Grun, R.; Eggleton, R.

    2003-12-01

    The establishment of a geochronological framework for weathering processes is essential for an understanding of the evolution of the regolith and its dynamics. However, there are few robust answers regarding the absolute age of weathering and its rates. Nowadays, 40Ar/39Ar analysis of Mn-Oxides (cryptomelane) and K-bearing secondary sulphates have provided one of the few generally reliable chronometers (e.g. 1), but is restricted to high-K secondary phases. This work presents a different approach to obtain geochronological information from weathering minerals, namely measurement of 238U-series disequilibria in authigenic Fe oxy/hydroxides. These may be potentially useful recorders of weathering processes as they commonly occur as weathering products and have high affinity towards dissolved uranyl complexes. Furthermore, U-Th fractionation during weathering has been extensively reported [2], effectively resetting the U/230Th geochronometer. LA-MC-ICP-MS facilitates in situ measurement of 238U-series disequilibria in authigenic microcrystalline iron oxy/hydroxides (precipitated between cracks and veins in partially and heavily weathered chlorite-muscovite schist) and pisoliths (ferruginous concretions). Contrary to previous studies [e.g. 3], in situ measurement of 238U-nuclides enables selective analysis or iron oxy/hydroxides phases, minimizes contributions from allogenic phases and, reduces the need of mathematical corrections to obtain the activity ratios for the authigenic phase [4, 5]. The results suggest that supergene iron oxy/hydroxides are good recorders of weathering processes; they precipitate during the early stages of weathering, reflect the U-isotopic composition of the groundwater, appear to act as closed-systems in weathering conservative environments, and behave in a predictable fashion when subjected to intense weathering and leaching conditions. The 230Th-ages of the iron oxy/hydroxides indicate that the timing and intensity of weathering appears

  11. New neutron-rich microsecond isomers observed among fission products of {sup 238}U at 80 MeV/nucleon

    SciTech Connect

    Folden, C. M. III; Ginter, T. N.; Hausmann, M.; Portillo, M.; Nettleton, A. S.; Amthor, A. M.; Sherrill, B. M.; Kubo, T.; Takeda, H.; Loveland, W.; Manikonda, S. L.; Morrissey, D. J.; Nakao, T.; Souliotis, G. A.; Strong, B. F.; Tarasov, O. B.

    2009-06-15

    Eight new isomeric states in neutron-rich nuclides have been discovered in fission fragments produced by the reaction of an 80 MeV/nucleon {sup 238}U beam with a {sup 9}Be target and separated in-flight using the A1900 fragment separator. The experiment was conducted at the National Superconducting Cyclotron Laboratory (NSCL) at Michigan State University. Gamma rays were detected in a high-purity germanium detector located at the focal plane within a time window of 20 {mu}s following ion implantation. In some cases the isomers were observed to decay into previously reported states, allowing us to assign the initial decay from the isomeric state. Among the outcomes, the results suggest that many studies on the nuclear structure of medium-mass neutron-rich nuclei are feasible at projectile fragmentation facilities using induced fission.

  12. Reactive transport of uranium in a groundwater bioreduction study: Insights from high-temporal resolution 238U/235U data

    NASA Astrophysics Data System (ADS)

    Shiel, A. E.; Johnson, T. M.; Lundstrom, C. C.; Laubach, P. G.; Long, P. E.; Williams, K. H.

    2016-08-01

    We conducted a detailed investigation of U isotopes in conjunction with a broad geochemical investigation during field-scale biostimulation and desorption experiments. This investigation was carried out in the uranium-contaminated alluvial aquifer of the Rifle field research site. In this well-characterized setting, a more comprehensive understanding of U isotope geochemistry is possible. Our results indicate that U isotope fractionation is consistently observed across multiple experiments at the Rifle site. Microbially-mediated reduction is suggested to account for most or all of the observed fractionation as abiotic reduction has been demonstrated to impart much smaller, often near-zero, isotopic fractionation or isotopic fractionation in the opposite direction. Data from some time intervals are consistent with a simple model for transport and U(VI) reduction, where the fractionation factor (ε = +0.65‰ to +0.85‰) is consistent with experimental studies. However, during other time intervals the observed patterns in our data indicate the importance of other processes in governing U concentrations and 238U/235U ratios. For instance, we demonstrate that departures from Rayleigh behavior in groundwater systems arise from the presence of adsorbed species. We also show that isotope data are sensitive to the onset of oxidation after biostimulation ends, even in the case where reduction continues to remove contaminant uranium downstream. Our study and the described conceptual model support the use of 238U/235U ratios as a tool for evaluating the efficacy of biostimulation and potentially other remedial strategies employed at Rifle and other uranium-contaminated sites.

  13. Uranium 238U/235U isotope ratios as indicators of reduction: results from an in situ biostimulation experiment at Rifle, Colorado, U.S.A.

    PubMed

    Bopp, Charles John; Lundstrom, Craig C; Johnson, Thomas M; Sanford, Robert A; Long, Philip E; Williams, Kenneth H

    2010-08-01

    The attenuation of groundwater contamination via chemical reaction is traditionally evaluated by monitoring contaminant concentration through time. However, this method can be confounded by common transport processes (e.g., dilution, sorption). Isotopic techniques bypass the limits of concentration methods, and so may provide improved accuracy in determining the extent of reaction. We apply measurements of 238U/235U to a U bioremediation field experiment at the Rifle Integrated Field Research Challenge Site in Rifle, Colorado. An array of monitoring and injection wells was installed on a 100 m2 plot where U(VI) contamination was present in the groundwater. Acetate-amended groundwater was injected along an up-gradient gallery to encourage the growth of dissimilatory metal reducing bacteria (e.g., Geobacter species). During amendment, U concentration dropped by an order of magnitude in the experiment plot. We measured 238U/235U in samples from one monitoring well by MC-ICP-MS using a double isotope tracer method. A significant approximately 1.00 per thousand decrease in 238U/235U occurred in the groundwater as U(VI) concentration decreased. The relationship between 238U/235U and concentration corresponds approximately to a Rayleigh distillation curve with an effective fractionation factor (alpha) of 1.00046. We attribute the observed U isotope fractionation to a nuclear field shift effect during enzymatic reduction of U(VI)(aq) to U(IV)(s).

  14. Predicted yields of new neutron-rich isotopes of nuclei with Z=64-80 in the multinucleon transfer reaction {sup 48}Ca+{sup 238}U

    SciTech Connect

    Adamian, G. G.; Antonenko, N. V.; Sargsyan, V. V.; Scheid, W.

    2010-05-15

    The production cross sections of new neutron-rich isotopes of nuclei with charge numbers Z=64-80 are estimated for future experiments in the multinucleon transfer reaction {sup 48}Ca+{sup 238}U at bombarding energy E{sub c.m.}=189 MeV close to the Coulomb barrier.

  15. Low export flux of particulate organic carbon in the central Arctic Ocean as revealed by 234Th:238U disequilibrium

    NASA Astrophysics Data System (ADS)

    Cai, P.; Rutgers van der Loeff, M.; Stimac, I.; NöThig, E.-M.; Lepore, K.; Moran, S. B.

    2010-10-01

    The loss of Arctic sea ice has accelerated in recent years. With the decline in sea ice cover, the Arctic Ocean biogeochemistry is undergoing unprecedented change. A key question about the changing Arctic Ocean biogeochemistry is concerning the impact of the shrinking sea ice cover on the particulate organic carbon (POC) export from the upper Arctic Ocean. Thus far, there are still very few direct measurements of POC export in the permanently ice-covered central Arctic Ocean. A further issue is that the magnitude of the POC export so far documented in this region remains controversial. During the ARK-XXII/2 expedition to the Arctic Ocean from 28 July to 7 October in 2007, we conducted a high-resolution study of POC export using 234Th/238U disequilibrium. Depth profiles of total 234Th in the upper 200 m were collected at 36 stations in the central Arctic Ocean and its adjacent seas, i.e., the Barents Sea, the Kara Sea and the Laptev Sea. Samples were processed using a small-volume MnO2 coprecipitation method with addition of a yield tracer, which resulted in one of the most precise 234Th data sets ever collected. Thorium-234 deficit with respect to 238U was found to be evident throughout the upper 100 m over the Arctic shelves. In comparison, 234Th deficit was confined to the upper 25 m in the central Arctic Ocean. Below 25 m, secular equilibrium was approached between 234Th and 238U. The observed 234Th deficit was generally associated with enhanced total chlorophyll concentrations, indicating that in situ production and export of biogenic particles are the main mechanism for 234Th removal in the Arctic Ocean. Thorium-234-derived POC fluxes were determined with a steady state model and pump-normalized POC/234Th ratios on total suspended particles collected at 100 m. Results showed enhanced POC export over the Arctic shelves. On average, POC export fluxes over the various Arctic shelves were 2.7 ± 1.7 mmol m-2 d-1 (the Barents Sea), 0.5 ± 0.8 mmol m-2 d-1 (the Kara

  16. Investigating Uranium Mobility Using Stable Isotope Partitioning of 238U/235U and a Reactive Transport Model

    NASA Astrophysics Data System (ADS)

    Bizjack, M.; Johnson, T. M.; Druhan, J. L.; Shiel, A. E.

    2015-12-01

    We report a numerical reactive transport model which explicitly incorporates the effectively stable isotopes of uranium (U) and the factors that influence their partitioning in bioactive systems. The model reproduces trends observed in U isotope ratios and concentration measurements from a field experiment, thereby improving interpretations of U isotope ratios as a tracer for U reactive transport. A major factor contributing to U storage and transport is its redox state, which is commonly influenced by the availability of organic carbon to support metal-reducing microbial communities. Both laboratory and field experiments have demonstrated that biogenic reduction of U(VI) fractionates the stable isotope ratio 238U/235U, producing an isotopically heavy solid U(IV) product. It has also been shown that other common reactive transport processes involving U do not fractionate isotopes to a consistently measurable level, which suggests the capacity to quantify the extent of bioreduction occurring in groundwater containing U using 238U/235U ratios. A recent study of a U bioremediation experiment at the Rifle IFRC site (Colorado, USA) applied Rayleigh distillation models to quantify U stable isotope fractionation observed during acetate amendment. The application of these simplified models were fit to the observations only by invoking a "memory-effect," or a constant source of low-concentration, unfractionated U(VI). In order to more accurately interpret the measured U isotope ratios, we present a multi-component reactive transport model using the CrunchTope software. This approach is capable of quantifying the cycling and partitioning of individual U isotopes through a realistic network of transport and reaction pathways including reduction, oxidation, and microbial growth. The model incorporates physical heterogeneity of the aquifer sediments through zones of decreased permeability, which replicate the observed bromide tracer, major ion chemistry, U concentration, and U

  17. Effect of projectile breakup on fission-fragment mass distributions in the Li,76 + 238U reactions

    NASA Astrophysics Data System (ADS)

    Santra, S.; Pal, A.; Rath, P. K.; Nayak, B. K.; Singh, N. L.; Chattopadhyay, D.; Behera, B. R.; Singh, Varinderjit; Jhingan, A.; Sugathan, P.; Golda, K. S.; Sodaye, S.; Appannababu, S.; Prasad, E.; Kailas, S.

    2014-12-01

    Background: Detailed studies on the effect of the breakup of weakly bound projectile on fission are scarce. Distinguishing the events of compound nuclear (CN) fission from the breakup or transfer induced fission to understand the properties of measured fission fragments is difficult but desirable. Purpose: To investigate the effect of projectile breakup and its breakup threshold energy on fission-fragment (FF) mass distributions and folding angle distributions for Li,76 + 238U reactions and find out the differences in the properties of the fission events produced by complete fusion (CF) from the total fusion (TF). Methods: The FF mass and folding angle distributions have been measured at energies around the Coulomb barrier using gas detectors by time-of-flight technique. The results are compared with the ones involving tightly bound projectiles as well as predictions from systematics to bring out the effect of the breakup. Results: A sharp increase in the peak to valley (P:V) ratio of FF mass distribution with the decrease in bombarding energy for Li,76 + 238U reactions is observed when all events are assumed to be CN fission. As the beam energy falls through the fusion barrier, the full width half maximum (FWHM) of the FF folding angle distribution is found to increase at sub-barrier energies, unlike the reactions involving tightly bound projectiles where a linear decrease in FWHM is expected. By selecting pure CN events from the scatter plot of the velocity components of the composite nuclei, the energy dependence of the deduced FWHM is found to be consistent with the ones involving tightly bound projectiles. Similarly, the P:V ratio obtained for the selected CN events is consistent with the theoretical calculations as well as the experimental data for the proton induced reaction forming similar CN. Conclusions: The presence of projectile breakup induced fission and a relatively low breakup threshold for 6Li compared to 7Li explains the observed differences in

  18. Rapid time scales of basalt to andesite differentiation at Anatahan volcano, Mariana Islands

    NASA Astrophysics Data System (ADS)

    Reagan, Mark; Tepley, Frank J.; Gill, James B.; Wortel, Matthew; Hartman, Brian

    2005-08-01

    We present comprehensive U-series data ( 238U- 234U- 230Th- 226Ra- 210Pb- 210Po and ( 230Th)/( 232Th)) for an andesite from an oceanic arc. The juvenile Anatahan andesite has U-Th systematics colinear with other historical Mariana volcanic rocks, and is most similar to those of the other volcano in the Mariana arc with a significant proportion of silicic andesite: Uracas. Like Uracas, the parental basalt for the Anatahan andesite was generated by relatively low degrees of flux melting from a source previously enriched in a sediment component from the subducting slab. However, the Anatahan andesite is much more strongly enriched in 226Ra over 230Th than Uracas lavas, and has one of the highest ( 226Ra)/( 232Th) ratios of siliceous andesites globally. The long-lived disequilibria between 238U- 230Th- 226Ra in the Anatahan andesite are inherited from basalt genesis, not created during differentiation or eruption. Thus, the time between genesis of the parental basalt and eruption of andesite at Anatahan is shorter than for Uracas. Moreover, the near-equilibrium ( 210Pb)/( 226Ra) value indicates that the magma body did not persistently lose or gain 222Rn for more than 2 years before eruption. This permits differentiation of the parental basalt to form andesite within this 2-year time period, although a differentiation time period between 100 and a few thousand years also is possible. The relative activities between 210Po and 210Pb suggest erupted scoria degassed Po less than most lavas despite eruption plume heights of ˜10 km, which further suggests an unusually rapid ascent before eruption. These data also show that juvenile material was ejected from the first day of the eruption. Phreatomagmatic ejecta overlying the main Anatahan scoria is strongly enriched in 210Po over 210Pb, indicating that a significant proportion of the Po degassed from rising magmas sublimes in its shallow fumarolic conduit system.

  19. Activity measurements of a suite of radionuclides (241Am, 239,240Pu, 238Pu, 238U, 234U, 235U, 232Th, 230Th, 228Th, 228Ra, 137Cs, 210Pb, 90Sr and 40K) in biota reference material (Ocean Shellfish): CCRI(II)-S3

    NASA Astrophysics Data System (ADS)

    Nour, S.; Karam, L. R.; Inn, K. G. W.

    2012-01-01

    In 2005, the CCRI decided that a comparison undertaken from 2002 to 2008 by the NIST (under the auspices of the Inter-America Metrology System [SIM]) in the development of a new biota (Ocean Shellfish) standard reference material (SRM) was sufficiently well constructed that it could be converted into a supplementary comparison under CCRI(II), with comparison identifier CCRI(II)-S3. This would enable the comparison to be used to support calibration and measurement capability (CMC) claims for radionuclide measurements in reference materials (specifically, animal-based organic materials). Previous comparisons of radionuclides have been of single or multiple nuclides in non-complex matrices and results of such could not be extended to support capabilities to measure the same nuclides in reference materials. The results of this comparison have been used to determine the certified reference value of the SRM. The key comparison working group (KCWG) of the CCRI(II) has approved this approach as a mechanism to link all the results to certified 'reference values' in lieu of the key comparison reference value (KCRV) of these specified radionuclides in this type of matrix (shellfish) so as to support CMCs of similar materials submitted by the present participants. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCRI, according to the provisions of the CIPM Mutual Recognition Arrangement (CIPM MRA).

  20. SUPPLEMENTARY COMPARISON: Activity measurements of a suite of radionuclides (40K, 137Cs, 210Pb, 210Po, 228Ra, 232Th, 234U, 235U, 238U, 238Pu, 239Pu, 239+240Pu, 241Am) in vegetal reference material (seaweed)

    NASA Astrophysics Data System (ADS)

    Outola, I.; Inn, K. G. W.; Karam, L. R.

    2008-01-01

    In 2005, the CCRI decided that a comparison undertaken from 2002 to 2005 by the NIST (SIM) in the development of a new seaweed standard reference material (SRM) was sufficiently well constructed that it could be converted into a supplementary comparison under CCRI(II), with comparison identifier CCRI(II)-S1, so as to support calibration and measurement capability (CMC) claims for radionuclide measurements in reference material (specifically, plant material). Previous comparisons of radionuclides have been of single or multiple nuclides in non-complex matrices and results of such could not be extended to support capabilities to measure the same nuclides in reference materials. The results of this comparison have been reported to the participants, and were also used to determine the certified reference values of the SRM. The key comparison working group (KCWG) of the CCRI(II) has approved this approach as a mechanism to link all the results to the certified 'reference values' in lieu of the key comparison reference value (KCRV) of these specified radionuclides in this type of matrix (vegetative) so as to support CMCs of similar materials. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCRI Section II, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA).

  1. SUPPLEMENTARY COMPARISON: Activity measurements of a suite of radionuclides (90Sr, 137Cs, 210Pb, 210Po, 228Ra, 234U, 235U, 238U, 238Pu, 239,240Pu) in soil reference material (Rocky Flats II): CCRI(II)-S2

    NASA Astrophysics Data System (ADS)

    Nour, S.; Inn, K. G. W.; Karam, L. R.

    2009-01-01

    In 2005, the CCRI decided that a comparison undertaken from 2002 to 2007 by the NIST (SIM) in the development of a new soil (Rocky Flats II) standard reference material (SRM) was sufficiently well constructed that it could be converted into a supplementary comparison under CCRI(II), with comparison identifier CCRI(II)-S2, so as to support calibration and measurement capability (CMC) claims for radionuclide measurements in reference material (specifically, low calcium-content soils). Previous comparisons of radionuclides have been of single or multiple nuclides in non-complex matrices and results of such could not be extended to support capabilities to measure the same nuclides in reference materials. The results of this comparison have been reported to the participants, and have been used to determine the certified reference value of the SRM. The key comparison working group (KCWG) of the CCRI(II) has approved this approach as a mechanism to link all the results to certified 'reference values' in lieu of the key comparison reference value (KCRV) of these specified radionuclides in this type of matrix (soil) so as to support CMCs of similar materials. Main text. To reach the main text of this paper, click on Final Report. Note that this text is that which appears in Appendix B of the BIPM key comparison database kcdb.bipm.org/. The final report has been peer-reviewed and approved for publication by the CCRI Section II, according to the provisions of the CIPM Mutual Recognition Arrangement (MRA).

  2. Comment on "Radiocarbon Calibration Curve Spanning 0 to 50,000 Years B.P. Based on Paired 230Th/234U/238U and 14C Dates on Pristine Corals" by R.G. Fairbanks, R. A. Mortlock, T.-C. Chiu, L. Cao, A. Kaplan, T. P. Guilderson, T. W. Fairbanks, A. L. Bloom, P

    SciTech Connect

    Reimer, P J; Baillie, M L; Bard, E; Beck, J W; Blackwell, P G; Buck, C E; Burr, G S; Edwards, R L; Friedrich, M; Guilderson, T P; Hogg, A G; Hughen, K A; Kromer, B; McCormac, G; Manning, S; Reimer, R W; Southon, J R; Stuiver, M; der Plicht, J v; Weyhenmeyer, C E

    2005-10-02

    Radiocarbon calibration curves are essential for converting radiocarbon dated chronologies to the calendar timescale. Prior to the 1980's numerous differently derived calibration curves based on radiocarbon ages of known age material were in use, resulting in ''apples and oranges'' comparisons between various records (Klein et al., 1982), further complicated by until then unappreciated inter-laboratory variations (International Study Group, 1982). The solution was to produce an internationally-agreed calibration curve based on carefully screened data with updates at 4-6 year intervals (Klein et al., 1982; Stuiver and Reimer, 1986; Stuiver and Reimer, 1993; Stuiver et al., 1998). The IntCal working group has continued this tradition with the active participation of researchers who produced the records that were considered for incorporation into the current, internationally-ratified calibration curves, IntCal04, SHCal04, and Marine04, for Northern Hemisphere terrestrial, Southern Hemisphere terrestrial, and marine samples, respectively (Reimer et al., 2004; Hughen et al., 2004; McCormac et al., 2004). Fairbanks et al. (2005), accompanied by a more technical paper, Chiu et al. (2005), and an introductory comment, Adkins (2005), recently published a ''calibration curve spanning 0-50,000 years''. Fairbanks et al. (2005) and Chiu et al. (2005) have made a significant contribution to the database on which the IntCal04 and Marine04 calibration curves are based. These authors have now taken the further step to derive their own radiocarbon calibration extending to 50,000 cal BP, which they claim is superior to that generated by the IntCal working group. In their papers, these authors are strongly critical of the IntCal calibration efforts for what they claim to be inadequate screening and sample pretreatment methods. While these criticisms may ultimately be helpful in identifying a better set of protocols, we feel that there are also several erroneous and misleading statements made by these authors which require a response by the IntCal working group. Furthermore, we would like to comment on the sample selection criteria, pretreatment methods, and statistical methods utilized by Fairbanks et al. in derivation of their own radiocarbon calibration.

  3. Retardation of [sup 238]U and [sup 232]Th decay chain radionuclides in Long Island and Connecticut aquifers

    SciTech Connect

    Copenhaver, S.A.; Krishnaswami, S.; Turekian, K.K. ); Epler, N.; Cochran, J.K. )

    1993-02-01

    Knowledge of the ability of an aquifer to retard the groundwater transport of toxic or radioactive ions can be inferred from the analysis of groundwater for the radionuclides of the [sup 238]U- and [sup 232]Th-decay chains. Groundwaters of varying chemical composition were analyzed from wells in Long Island, New York, and Connecticut. Aquifer lithologies are arkose, quartz sandstone, granite, and glacial drift. Adsorption (k[sub 1]) and desorption (k[sub 2]) coefficients for Ra and Pb were calculated using [sup 222]Rn activity as a measure of the supply of other [alpha]-recoil nuclides. Laboratory tests of the validity of this assumption were made by measuring the flux of [sup 224]Ra and [sup 222]Rn from aquifer solids. The ratio k[sub 1]/k[sub 2] is the distribution coefficient, K, which is effective equal to R[sub f], the retardation factor. The average value of K for Ra is 6 [times] 10[sup 2] in Long Island aquifers and 5 [times] 10[sup 4] in Connecticut. The distribution coefficient for Pb is 10[sup 4] in Long Island and 10[sup 5] in Connecticut. Results from this and other studies reveal a strong dependence of retardation on pH, f[sub o[sub 2

  4. Comparative measurement of prompt fission γ -ray emission from fast-neutron-induced fission of 235U and 238U

    NASA Astrophysics Data System (ADS)

    Lebois, M.; Wilson, J. N.; Halipré, P.; Oberstedt, A.; Oberstedt, S.; Marini, P.; Schmitt, C.; Rose, S. J.; Siem, S.; Fallot, M.; Porta, A.; Zakari, A.-A.

    2015-09-01

    Prompt fission γ -ray (PFG) spectra have been measured in a recent experiment with the novel directional fast-neutron source LICORNE at the ALTO facility of the IPN Orsay. These first results from the facility involve the comparative measurement of prompt γ emission in fast-neutron-induced fission of 235U and 238U . Characteristics such as γ multiplicity and total and average radiation energy are determined in terms of ratios between the two systems. Additionally, the average photon energies were determined and compared with recent data on thermal-neutron-induced fission of 235U . PFG spectra are shown to be similar within the precision of the present measurement, suggesting that the extra incident energy does not significantly impact the energy released by prompt γ rays. The origins of some small differences, depending on either the incident energy or the target mass, are discussed. This study demonstrates the potential of the present approach, combining an innovative neutron source and new-generation detectors, for fundamental and applied research on fission in the near future.

  5. Fission-fragment properties in 238U(n ,f ) between 1 and 30 MeV

    NASA Astrophysics Data System (ADS)

    Duke, D. L.; Tovesson, F.; Laptev, A. B.; Mosby, S.; Hambsch, F.-J.; Bryś, T.; Vidali, M.

    2016-11-01

    The fragment mass and kinetic energy in neutron-induced fission of 238U has been measured for incident energies from 1 to 30 MeV at the Los Alamos Neutron Science Center. The change in mass distributions over this energy range were studied, and the transition from highly asymmetric to more symmetric mass distributions is observed. A decrease in average total kinetic energy (TKE ¯) with increasing excitation energy is observed, consistent with previous experimental work. Additional structure at multichance fission thresholds is present in the TKE ¯ data. The correlations between fragment masses and total kinetic energy and how that changes with excitation energy of the fissioning compound nucleus were also measured. The fission mass yields and average total kinetic energy are important for fission-based technologies such as nuclear reactors to understand nuclear waste generation and energy output when developing new and advanced concepts. The correlations between fragment mass and kinetic energy are needed both as input for theoretical calculations of the deexcitation process in fission fragments by prompt radiation emission and for validating advanced theoretical fission models describing the formation of the primordial fragments.

  6. Gamma-Ray Emission Spectra as a Constraint on Calculations of 234 , 236 , 238U Neutron-Capture Cross Sections

    NASA Astrophysics Data System (ADS)

    Ullmann, J. L.; Krticka, M.; Kawano, T.; Bredeweg, T. A.; Baramsai, B.; Couture, A.; Haight, R. C.; Jandel, M.; Mosby, S.; O'Donnell, J. M.; Rundberg, R. S.; Vieira, D. J.; Wilhelmy, J. B.; Becker, J. A.; Wu, C. Y.; Chyzh, A.

    2015-10-01

    Calculations of the neutron-capture cross section at low neutron energies (10 eV through 100's of keV) are very sensitive to the nuclear level density and radiative strength function. These quantities are often poorly known, especially for radioactive targets, and actual measurements of the capture cross section are usually required. An additional constraint on the calculation of the capture cross section is provided by measurements of the cascade gamma spectrum following neutron capture. Recent measurements of 234 , 236 , 238U(n, γ) emission spectra made using the DANCE 4 π BaF2 array at the Los Alamos Neutron Science Center will be presented. Calculations of gamma-ray spectra made using the DICEBOX code and of the capture cross section made using the CoH3 code will also be presented. These techniques may be also useful for calculations of more unstable nuclides. This work was performed with the support of the U.S. Department of Energy, National Nuclear Security Administration by Los Alamos National Security, LLC (Contract DE-AC52-06NA25396) and Lawrence Livermore National Security, LLC (Contract DE-AC52-07NA2734).

  7. The CIELO Collaboration: Neutron Reactions on 1H, 16O, 56Fe, 235,238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Chadwick, M. B.; Dupont, E.; Bauge, E.; Blokhin, A.; Bouland, O.; Brown, D. A.; Capote, R.; Carlson, A.; Danon, Y.; De Saint Jean, C.; Dunn, M.; Fischer, U.; Forrest, R. A.; Frankle, S. C.; Fukahori, T.; Ge, Z.; Grimes, S. M.; Hale, G. M.; Herman, M.; Ignatyuk, A.; Ishikawa, M.; Iwamoto, N.; Iwamoto, O.; Jandel, M.; Jacqmin, R.; Kawano, T.; Kunieda, S.; Kahler, A.; Kiedrowski, B.; Kodeli, I.; Koning, A. J.; Leal, L.; Lee, Y. O.; Lestone, J. P.; Lubitz, C.; MacInnes, M.; McNabb, D.; McKnight, R.; Moxon, M.; Mughabghab, S.; Noguere, G.; Palmiotti, G.; Plompen, A.; Pritychenko, B.; Pronyaev, V.; Rochman, D.; Romain, P.; Roubtsov, D.; Schillebeeckx, P.; Salvatores, M.; Simakov, S.; Soukhovitskiı˜, E. Sh.; Sublet, J. C.; Talou, P.; Thompson, I.; Trkov, A.; Vogt, R.; van der Marck, S.

    2014-04-01

    CIELO (Collaborative International Evaluated Library Organization) provides a new working paradigm to facilitate evaluated nuclear reaction data advances. It brings together experts from across the international nuclear reaction data community to identify and document discrepancies among existing evaluated data libraries, measured data, and model calculation interpretations, and aims to make progress in reconciling these discrepancies to create more accurate ENDF-formatted files. The focus will initially be on a small number of the highest-priority isotopes, namely 1H, 16O, 56Fe, 235,238U, and 239Pu. This paper identifies discrepancies between various evaluations of the highest priority isotopes, and was commissioned by the OECD's Nuclear Energy Agency WPEC (Working Party on International Nuclear Data Evaluation Co-operation) during a meeting held in May 2012. The evaluated data for these materials in the existing nuclear data libraries - ENDF/B-VII.1, JEFF-3.1, JENDL-4.0, CENDL-3.1, ROSFOND, IRDFF 1.0 - are reviewed, discrepancies are identified, and some integral properties are given. The paper summarizes a program of nuclear science and computational work needed to create the new CIELO nuclear data evaluations.

  8. Photo-fission Product Yield Measurements at Eγ=13 MeV on 235U, 238U, and 239Pu

    NASA Astrophysics Data System (ADS)

    Tornow, W.; Bhike, M.; Finch, S. W.; Krishichayan, Fnu; Tonchev, A. P.

    2016-09-01

    We have measured Fission Product Yields (FPYs) in photo-fission of 235U, 238U, and 239Pu at TUNL's High-Intensity Gamma-ray Source (HI γS) using mono-energetic photons of Eγ = 13 MeV. Details of the experimental setup and analysis procedures will be discussed. Yields for approximately 20 fission products were determined. They are compared to neutron-induced FPYs of the same actinides at the equivalent excitation energies of the compound nuclear systems. In the future photo-fission data will be taken at Eγ = 8 . 0 and 10.5 MeV to find out whether photo-fission exhibits the same so far unexplained dependence of certain FPYs on the energy of the incident probe, as recently observed in neutron-induced fission, for example, for the important fission product 147Nd. Work supported by the U. S. Dept. of Energy, under Grant No. DE-FG02-97ER41033, and by the NNSA, Stewardship Science Academic Alliances Program, Grant No. DE-NA0001838 and the Lawrence Livermore, National Security, LLC under Contract No. DE-AC52-07NA27344.

  9. Simultaneous determination of gross alpha, gross beta and ²²⁶Ra in natural water by liquid scintillation counting.

    PubMed

    Fons, J; Zapata-García, D; Tent, J; Llauradó, M

    2013-11-01

    The determination of gross alpha, gross beta and (226)Ra activity in natural waters is useful in a wide range of environmental studies. Furthermore, gross alpha and gross beta parameters are included in international legislation on the quality of drinking water [Council Directive 98/83/EC]. In this work, a low-background liquid scintillation counter (Wallac, Quantulus 1220) was used to simultaneously determine gross alpha, gross beta and (226)Ra activity in natural water samples. Sample preparation involved evaporation to remove (222)Rn and its short-lived decay daughters. The evaporation process concentrated the sample ten-fold. Afterwards, a sample aliquot of 8 mL was mixed with 12 mL of Ultima Gold AB scintillation cocktail in low-diffusion vials. In this study, a theoretical mathematical model based on secular equilibrium conditions between (226)Ra and its short-lived decay daughters is presented. The proposed model makes it possible to determine (226)Ra activity from two measurements. These measurements also allow determining gross alpha and gross beta simultaneously. To validate the proposed model, spiked samples with different activity levels for each parameter were analysed. Additionally, to evaluate the model's applicability in natural water, eight natural water samples from different parts of Spain were analysed. The eight natural water samples were also characterised by alpha spectrometry for the naturally occurring isotopes of uranium ((234)U, (235)U and (238)U), radium ((224)Ra and (226)Ra), (210)Po and (232)Th. The results for gross alpha and (226)Ra activity were compared with alpha spectrometry characterization, and an acceptable concordance was obtained.

  10. Particulate organic carbon export from the North and South Atlantic gyres: The 234Th/ 238U disequilibrium approach

    NASA Astrophysics Data System (ADS)

    Thomalla, Sandy; Turnewitsch, Robert; Lucas, Mike; Poulton, Alex

    2006-07-01

    Subtropical ocean gyres are believed to be characterized by low carbon export from the surface into the deep ocean. However, due to their large areas, even relatively small average export could be of significance for the global carbon cycle. To better constrain carbon export from the surface ocean in such regions, radioactive disequilibria between the particle-reactive, short-lived radionuclide 234Th (half-life 24.1 d) and its parent 238U were used to estimate fluxes of 234Th and particulate organic carbon (POC) from surface waters of the North and South Atlantic subtropical gyres and their fringes. Samples were collected between ˜50°S and ˜50°N as part of the Atlantic Meridional Transect (AMT) programme during April/May 2004 (AMT14). Application of a steady-state model to the 234Th data revealed particle export from the surface ( 234Th deficit) and, in one instance, some evidence for shallow particle remineralisation at depth ( 234Th excess). Export fluxes of POC were calculated from water column 234Th / 238U disequilibria and the POC to 234Th ratios on large rapidly sinking particles (>50 μm). Based on latitudinal distributions of selected hydrographic and biological parameters within the topmost 300 m of the water column, the transect was divided into six regions: 'temperate' (35°-50°N and 35°-50°S), 'oligotrophic' (20°-35°N and 5°-35°S), 'equatorial' (5°S-5°N), and 'upwelling' (5°-20°N). The lowest 234Th-derived POC export fluxes were found in the oligotrophic gyres and ranged from 0 in the northern to 6 mmol C m -2 d -1 in the southern oligotrophic, indicating a tightly coupled food web. Enhanced POC export was associated with the equatorial region (25 mmol C m -2 d -1) and the upwelling region north of the equator (15 mmol C m -2 d -1). POC export in the temperate regions ranged from 7 mmol C m -2 d -1 to a maximum of 41 mmol C m -2 d -1. High fluxes at the poleward edges of the oligotrophic gyres probably result from episodic nutrient

  11. Resonance Region Covariance Analysis Method and New Covariance Data for {sup 232}Th, {sup 233}U, {sup 235}U, {sup 238}U, and {sup 239}Pu

    SciTech Connect

    Leal, L.C. Arbanas, G.; Wiarda, D.; Derrien, H.

    2008-12-15

    Resonance-parameter covariance matrix (RPCM) evaluations in the resolved resonance region were done for {sup 232}Th, {sup 233}U, {sup 235}U, {sup 238}U, and {sup 239}Pu using the computer code SAMMY. The retroactive approach of the code SAMMY was used to generate the RPCMs for {sup 233}U and {sup 235}U. RPCMs for {sup 232}Th, {sup 238}U and {sup 239}Pu were generated together with the resonance parameter evaluations. The RPCMs were then converted in the ENDF format using the File32 representation. Alternatively, for computer storage reasons, the File32 was converted in the File33 cross section covariance matrix (CSCM). Both representations were processed using the computer code PUFF-IV. This paper describes the procedures used to generate the RPCM with SAMMY.

  12. Low-energy fission investigated in reactions of 750 AMeV238U-ions with Pb and Be targets. I. Nuclear charge distributions

    NASA Astrophysics Data System (ADS)

    Armbruster, P.; Bernas, M.; Czajkowski, S.; Geissel, H.; Aumann, T.; Dessagne, Ph.; Donzaud, C.; Hanelt, E.; Heinz, A.; Hesse, M.; Kozhuharov, C.; Miehe, Ch.; Münzenberg, G.; Pfützner, M.; Schmidt, K.-H.; Schwab, W.; Stéphan, C.; Sümmerer, K.; Tassan-Got, L.; Voss, B.

    1996-12-01

    Charge distributions of fragments from low energy nuclear fission are investigated in reactions of highly fissile238U projectiles at relativistic energies (750 A·MeV) with a heavy (Pb) and a light (Be) target. The fully stripped fission fragments are separated by the Fragment Separator (FRS). Their high kinetic energies in the laboratory system allow the identification of all atomic numbers by using Multiple-Sampling Ionization Chambers (MUSIC). The elemental distributions of fragments observed at larger magnetic rigidities than the238U projectiles show asymmetric break-up and odd-even effects. They indicate a low energy fission process, induced mainly by dissociation in the electro-magnetic field for the U/Pb-system, or by peripheral nuclear interactions for the U/Be-system.

  13. Towards the high-accuracy determination of the 238U fission cross section at the threshold region at CERN - n_TOF

    NASA Astrophysics Data System (ADS)

    Diakaki, M.; Audouin, L.; Berthoumieux, E.; Calviani, M.; Colonna, N.; Dupont, E.; Duran, I.; Gunsing, F.; Leal-Cidoncha, E.; Le Naour, C.; Leong, L. S.; Mastromarco, M.; Paradela, C.; Tarrio, D.; Tassan-Got, L.; Aerts, G.; Altstadt, S.; Alvarez, H.; Alvarez-Velarde, F.; Andriamonje, S.; Andrzejewski, J.; Badurek, G.; Barbagallo, M.; Baumann, P.; Becares, V.; Becvar, F.; Belloni, F.; Berthier, B.; Billowes, J.; Boccone, V.; Bosnar, D.; Brugger, M.; Calvino, F.; Cano-Ott, D.; Capote, R.; Carrapiço, C.; Cennini, P.; Cerutti, F.; Chiaveri, E.; Chin, M.; Cortes, G.; Cortes-Giraldo, M. A.; Cosentino, L.; Couture, A.; Cox, J.; David, S.; Dillmann, I.; Domingo-Pardo, C.; Dressler, R.; Dridi, W.; Eleftheriadis, C.; Embid-Segura, M.; Ferrant, L.; Ferrari, A.; Finocchiaro, P.; Fraval, K.; Fujii, K.; Furman, W.; Ganesan, S.; Garcia, A. R.; Giubrone, G.; Gomez-Hornillos, M. B.; Goncalves, I. F.; Gonzalez-Romero, E.; Goverdovski, A.; Gramegna, F.; Griesmayer, E.; Guerrero, C.; Gurusamy, P.; Haight, R.; Heil, M.; Heinitz, S.; Igashira, M.; Isaev, S.; Jenkins, D. G.; Jericha, E.; Kadi, Y.; Kaeppeler, F.; Karadimos, D.; Karamanis, D.; Kerveno, M.; Ketlerov, V.; Kivel, N.; Kokkoris, M.; Konovalov, V.; Krticka, M.; Kroll, J.; Lampoudis, C.; Langer, C.; Lederer, C.; Leeb, H.; Lo Meo, S.; Losito, R.; Lozano, M.; Manousos, A.; Marganiec, J.; Martinez, T.; Marrone, S.; Massimi, C.; Mastinu, P.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mingrone, F.; Mirea, M.; Mondelaers, W.; Moreau, C.; Mosconi, M.; Musumarra, A.; O'Brien, S.; Pancin, J.; Patronis, N.; Pavlik, A.; Pavlopoulos, P.; Perkowski, J.; Perrot, L.; Pigni, M. T.; Plag, R.; Plompen, A.; Plukis, L.; Poch, A.; Pretel, C.; Praena, J.; Quesada, J.; Rauscher, T.; Reifarth, R.; Riego, A.; Roman, F.; Rudolf, G.; Rubbia, C.; Rullhusen, P.; Salgado, J.; Santos, C.; Sarchiapone, L.; Sarmento, R.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Stephan, C.; Tagliente, G.; Tain, J. L.; Tavora, L.; Terlizzi, R.; Tsinganis, A.; Valenta, S.; Vannini, G.; Variale, V.; Vaz, P.; Ventura, A.; Versaci, R.; Vermeulen, M. J.; Villamarin, D.; Vincente, M. C.; Vlachoudis, V.; Vlastou, R.; Voss, F.; Wallner, A.; Walter, S.; Ware, T.; Weigand, M.; Weiß, C.; Wiesher, M.; Wisshak, K.; Wright, T.; Zugec, P.

    2016-03-01

    The 238U fission cross section is an international standard beyond 2 MeV where the fission plateau starts. However, due to its importance in fission reactors, this cross-section should be very accurately known also in the threshold region below 2 MeV. The 238U fission cross section has been measured relative to the 235U fission cross section at CERN - n_TOF with different detection systems. These datasets have been collected and suitably combined to increase the counting statistics in the threshold region from about 300 keV up to 3 MeV. The results are compared with other experimental data, evaluated libraries, and the IAEA standards.

  14. Uranium 238U/235U isotope ratios as indicators of reduction: Results from an in situ biostimulation experiment at Rifle, Colorado, USA

    SciTech Connect

    Bopp IV, C.J.; Lundstrom, C.C.; Johnson, T.M.; Sanford, R.A.; Long, P.E.; Williams, K.H.

    2010-02-01

    The attenuation of groundwater contamination via chemical reaction is traditionally evaluated by monitoring contaminant concentration through time. However, this method can be confounded by common transport processes (e.g. dilution, sorption). Isotopic techniques bypass the limits of concentration methods, and so may provide improved accuracy in determining the extent of reaction. We apply measurements of {sup 238}U/{sup 235}U to a U bioremediation field experiment at the Rifle Integrated Field Research Challenge Site in Rifle, Colorado (USA). An array of monitoring and injection wells was installed on a 100 m{sup 2} plot where U(VI) contamination was present in the groundwater. Acetate-amended groundwater was injected along an up-gradient gallery to encourage the growth of dissimilatory metal reducing bacteria (e.g. Geobacter species). During amendment, U concentration dropped by an order of magnitude in the experiment plot. We measured {sup 238}U/{sup 235}U in samples from one monitoring well by MC-ICP-MS using a double isotope tracer method. A significant {approx}1.00{per_thousand} decrease in {sup 238}U/{sup 235}U occurred in the groundwater as U(VI) concentration decreased. The relationship between {sup 238}U/{sup 235}U and concentration corresponds approximately to a Rayleigh distillation curve with an effective fractionation factor ({alpha}) of 1.00046. We attribute the observed U isotope fractionation to a nuclear field shift effect during enzymatic reduction of U(VI){sub (aq)} to U(IV){sub (s)}.

  15. Intermediate mass fragment emission in 32S + 51V, 109Ag, and 238U collisions at E = 31.6 MeV A

    NASA Astrophysics Data System (ADS)

    Machner, H.; Nolte, M.; Palarczyk, M.; Kutsarova, T.

    2015-11-01

    Intermediate mass fragment emission for reactions of 32S + 51V, 109Ag, and 238U has been studied. Double differential cross sections were analysed in terms of the generalised moving source model yielding charge distributions. Isotope ratios show strong fragment mass dependencies. The data were successfully reproduced by the coalescence model as well as by statistical multifragmentation model calculations. Quantum molecular dynamics model calculations were not so successful.

  16. Comparison of activity concentration of 238U, 232Th and 40K in different Layers of subsurface Structures in Dei-Dei and Kubwa, Abuja, northcentral Nigeria

    NASA Astrophysics Data System (ADS)

    Maxwell, Omeje; Wagiran, Husin; Ibrahim, Noorddin; Lee, Siak Kuan; Sabri, Soheil

    2013-10-01

    The study of activity concentration of 232Th, 238U and 40K of rock samples from site one (S1L1-S1L11, 70 m) and site two (S2L1-S2L9, 60 m) boreholes in Dei-Dei and Kubwa was presented and the first time in the region to be compared. Activity concentrations were analysed using a high resolution co-axial HPGe gamma ray spectrometer system. The activity concentration ranges in site one borehole were from 45±1 to 98±6 Bq kg-1 for 232Th, from 18±2 to 37±4 Bq kg-1 for 238U and from 254 ±32 Bq kg-1 to 1195 ±151 Bq kg-1 for 40K. The activity concentration ranges in site two borehole were from 32±3 to 84±7 Bq kg-1 for 232Th, from 15±2 to 52±5 Bq kg-1 for 238U and from 119±15 to 705±94 for 40K Bq kg-1. Significantly higher concentration of 232Th and 238U occurs in samples collected from S1L7, S1L11 and S2L1 layers. These zones experienced granitic intrusions produced by denudation and tectonism. 40K in rock samples of S1L4 and S2L4 activity concentrations is close; it could be that biotite granitic intrusion that is inferred as the formation in that layer reflects the same activity of potassium in rock's radioactivity measurement. The area requires further investigation of soil geochemistry and activity concentration of radionuclides in groundwater.

  17. Assay Methods for 238U, 232Th, and 210Pb in Lead and Calibration of 210Bi Bremsstrahlung Emission from Lead

    SciTech Connect

    Orrell, John L.; Aalseth, Craig E.; Arnquist, Isaac J.; Eggemeyer, Tere A.; Glasgow, Brian D.; Hoppe, Eric W.; Keillor, Martin E.; Morley, Shannon M.; Myers, Allan W.; Overman, Cory T.; Shaff, Sarah M.; Thommasson, Kimbrelle S.

    2016-02-13

    Assay methods for measuring 238U, 232Th, and 210Pb concentrations in refined lead are presented. The 238U and 232Th concentrations are assayed via inductively coupled plasma mass spectrometry (ICP-MS) after anion exchange column separation on dissolved lead samples. The 210Pb concentration is inferred through α-spectroscopy of a daughter isotope, 210Po, after chemical precipitation separation on dissolved lead samples. Subsequent to the 210Po α-spectroscopy assay, a method for evaluating 210Pb concentrations in solid lead samples was developed via measurement of bremsstrahlung radiation from β-decay of a daughter isotope, 210Bi, by employing a 14-crystal array of high purity germanium (HPGe) detectors. Ten sources of refined lead were assayed. The 238U concentrations were <34 microBq/kg and the 232Th concentrations ranged <0.6 – 15 microBq/kg, as determined by the ICP-MS assay method. The 210Pb concentrations ranged from ~0.1 – 75 Bq/kg, as inferred by the 210Po α-spectroscopy assay method.

  18. Thorium-uranium disequilibrium dating of Late Quaternary ferruginous concretions and rinds

    NASA Astrophysics Data System (ADS)

    Short, Stephen A.; Lowson, Richard T.; Ems, John; Price, David M.

    1989-06-01

    Radioactive ferruginous nodules from the Alligator Rivers Uranium Province, Northern Territory, Australia, were systematically examined by optical microscopy, XRD, alpha- and fission-track autoradiography, and analysed for U, Th, Ra and major stable elements. Correlation of autoradiographs with microscopic structure and analyses of selective extractions confirmed that U and Th were strongly associated with Fe oxides. Fission-track autoradiography showed no concentration gradient evidence for postdepositional leaching of uranium. Strong acid leaching studies showed that irreversibly adsorbed U, and authigenic 234U and 230Th, but not 226Ra, are quantitatively retained by accumulated oxide/oxyhydroxide. Correlation of the groundwater activity ratio with oxidic 234U/ 238U activity ratios indicated the latter was radiogenically consistent with oxidic 230Th/ 234U activity ratios < 1. Dense, accumulated Fe/Mn oxide matrices are apparently capable of forming radiogenic closed systems in respect of the 230U → 234U → 230Th decay set. 234U/ 238U and 230Th/ 234U activity ratios were used to derive similar mean ages of rinds for four nodules in the same horizon. Th/U ages were also determined, using a Th-index detrital correction method previously used for impure carbonates, of pedogenic Fe/Mn accumulations having background concentrations of U and Th from other locations in Australia. These ages were compared with TL and 14C ages of the-host sediments. The comparisions suggest that Th/U dating could be used to age indurated layers of Fe/Mn oxides in soil horizons < 350 ka old.

  19. Radon in spring waters in the south of Catalonia.

    PubMed

    Fonollosa, E; Peñalver, A; Borrull, F; Aguilar, C

    2016-01-01

    Spring waters in the south of Catalonia were analysed to determine the (222)Rn activity in order to be able to establish a correlation between the obtained values with the geology of the area of origin of these samples, and also estimate the potential health risks associated with (222)Rn. Most of the analysed samples (90%) show (222)Rn activities lower than 100Bq/L (exposure limit in water recommended by the World Health Organisation and EU directive 2013/51/EURATOM). However, in some cases, the activity values found for this isotope exceeded those levels and this can be attributed to the geology of the area where the spring waters are located, which is predominantly of granitic characteristics. To verify the origin of the radon present in the analysed samples, the obtained activity values were compared with the activities of its parents ((226)Ra, (238)U and (234)U). Finally, we have calculated the annual effective dose from all the radionuclides measured in spring water samples. The results showed that the higher contribution due to spring water ingestion come from (222)Rn and (226)Ra. The resulting contribution to the annual effective dose due to radon ingestion varies between 10.2 and 765.8 μSv/y, and the total annual effective dose due to his parents, (226)Ra, (234)U and (238)U varies between 0.8 and 21.2 μSv/y so the consumption of these waters does not involve any risks to population due to its natural radioactivity content.

  20. Resolving the early chronology of Mono Craters volcanism with combined 238U-230Th and 40Ar/39Ar dating

    NASA Astrophysics Data System (ADS)

    Vazquez, J. A.; Calvert, A. T.; Marcaida, M.; Mangan, M.; Lidzbarski, M. I.; Stelten, M. E.

    2013-12-01

    California's largest locus of Pleistocene-Holocene rhyolitic volcanism is the Mono Lake-Long Valley region of eastern California. The Mono Craters chain marks the northern portion of this locus, and is composed of at least 28 individual domes of high-silica rhyolite. The record of Holocene volcanism at Mono Craters is relatively well constrained by tephrostratigraphy and radiocarbon dating. However, the timing and frequency of late Pleistocene dome emplacement is poorly resolved, with most of the chronology based on hydration-rind dating of obsidian. A well-exposed archive of late Pleistocene volcanism from Mono Craters is recorded by tephra beds (ashes numbered 1-19, youngest to oldest) of the informal Wilson Creek formation that accumulated in ancestral Mono Lake. To resolve a precise chronology for late Pleistocene volcanism at Mono Craters and tune the time-series of explosive volcanism preserved by Wilson Creek tephras, we performed ion microprobe 238U-230Th dating of allanite and zircon together with laser-fusion 40Ar/39Ar dating of sanidine from rhyolite domes that yield the oldest hydration rind ages and have relatively subdued morphology. Sanidine from multiple domes, including both hornblende-biotite and fayalite-bearing rhyolite types, yield 40Ar/39Ar ages up to ca. 25 ka. Ion microprobe analyses of unpolished rims on indium-mounted allanite and zircon crystals yield U-Th isochron ages that are indistinguishable from their associated sanidine 40Ar/39Ar ages. However, the interiors of sectioned allanite crystals yield model U-Th ages that may be up to 30 kyr older than their rims. Rims on allanite and zircon from ashes 7-19 in the lower portion of the Wilson Creek stratigraphy yield isochron ages of ca. 27-62 ka [1], which are supported by ages from magnetostratigraphy [2]. Ash 3 contains titanomagnetites that are compositionally distinct from other Wilson Creek tephras, but match those in the hornblende-biotite rhyolite of dome 11. Rims on allanite and

  1. Reconstruction of the 236U input function for the Northeast Atlantic Ocean: Implications for 129I/236U and 236U/238U-based tracer ages

    NASA Astrophysics Data System (ADS)

    Christl, Marcus; Casacuberta, Núria; Vockenhuber, Christof; Elsässer, Christoph; Bailly du Bois, Pascal; Herrmann, Jürgen; Synal, Hans-Arno

    2015-11-01

    A reconstruction of historical discharges of 236U into the Northeast Atlantic Ocean by nuclear installations is presented. The nuclear reprocessing facilities Sellafield (SF), Great Britain (GB) and La Hague (LH), France and potentially also the nuclear fuel processing installation Springfields (SP), GB represent the main contributors of 236U in the Northeast Atlantic Ocean. Because data on 236U releases is lacking, 236U discharges from SP and SF are estimated based on the U-isotopic systematics found in the discharges from LH. The resulting reconstruction of 236U releases indicates that, until 2013, a total of (95 ± 32) kg of 236U was discharged from SF, SP, and LH. In a second step, the reconstructed 236U releases are combined with 129I data from literature and oceanic and atmospheric box models are used to derive the 129I/236U and 236U/238U input functions that, for example, can be used to calculate tracer ages of Atlantic Waters in the Arctic Ocean. Our conceptual results show that the combination of 129I/236U and 236U/238U generally allows the estimation of tracer ages over the past approximately 25 years if contributions of 236U from global fallout are considered. Finally, as a proof of concept, the new method is applied to calculate tracer ages of Arctic Ocean surface samples (collected in 2011/2012) and the results are in good agreement with literature data. We conclude that the combination of 129I/236U with 236U/238U in a dual tracer approach provides a sensitive tool for the calculation of tracer ages and ventilation rates in the North Atlantic region.

  2. EXCALIBUR-at-CALIBAN: a neutron transmission experiment for {sup 238}U(n,n'{sub continuum}γ) nuclear data validation

    SciTech Connect

    Bernard, David; Leconte, Pierre; Destouches, Christophe; Casoli, Pierre; Chambru, Laurent; Chanussot, Didier; Chateauvieux, Herve; Gevrey, Gaetan; Guilbert, Frederique; Lereuil, Hugues; Rousseau, Guillaume; Schaub, Muriel; Heusch, Murielle; Meplan, Olivier; Ramdhane, Mourad

    2015-07-01

    Two recent papers justified a new experimental program to give a new basis for the validation of {sup 238}U nuclear data, namely neutron induced inelastic scattering and transport codes at neutron fission energies. The general idea is to perform a neutron transmission experiment through natural uranium material. As shown by Hans Bethe, neutron transmissions measured by dosimetric responses are linked to inelastic cross sections. This paper describes the principle and the results of such an experience called EXCALIBUR performed recently (January and October 2014) at the CALIBAN reactor facility. (authors)

  3. Violence of heavy-ion reactions from neutron multiplicity: 11 to 20A-italic MeV /sup 20/Ne+ /sup 238/U

    SciTech Connect

    Jahnke, U.; Ingold, G.; Hilscher, D.; Lehmann, M.; Schwinn, E.; Zank, P.

    1986-07-14

    The suitability of the neutron multiplicity as a gauge for the violence of medium-energy heavy-ion reactions is investigated for the first time. For this purpose the number of neutrons emitted from fission reactions induced by 220-, 290-, and 400-MeV /sup 20/Ne on /sup 238/U is registered event-by-event with a large 4..pi.. scintillator tank. It is shown that the neutron multiplicity is indeed closely related to the two quantities characterizing the violence: the induced total intrinsic excitation and the linear momentum transfer.

  4. Comparison of the (p,xn) cross sections from /sup 238/U, /sup 235/U, and /sup 232/Th targets irradiated with 200-MeV protons

    SciTech Connect

    Chu, Y.Y.; Zhou, M.L.

    1982-01-01

    We have measured absolute cross sections for (p,xn) reactions (x ranges from 0 to 8) from /sup 238/U, /sup 235/U, and /sup 232/Th targets irradiated with 200-MeV protons at the Brookhaven AGS Linac injector. Chemical yields were determined by using /sup 239/Np and /sup 233/Pa as tracers. Yield patterns obtained in this work can be compared to the experimental results and theoretical calculations from earlier work, and they are consistent within the framework of intranuclear cascade followed by neutron evaporation and fission competition.

  5. Accurate measurements of fission-fragment yields in 234,235,236,238U(γ,f) with the SOFIA set-up

    NASA Astrophysics Data System (ADS)

    Chatillon, A.; Taïeb, J.; Martin, J.-F.; Pellereau, E.; Boutoux, G.; Gorbinet, T.; Grente, L.; Bélier, G.; Laurent, B.; Alvarez-Pol, H.; Ayyad, Y.; Benlliure, J.; Caamaño, M.; Audouin, L.; Casarejos, E.; Cortina-Gil, D.; Farget, F.; Fernández-Domínguez, B.; Heinz, A.; Jurado, B.; Kelić-Heil, A.; Kurz, N.; Lindberg, S.; Löher, B.; Nociforo, C.; Paradela, C.; Pietri, S.; Ramos, D.; Rodriguez-Sanchez, J.-L.; Rodrìguez-Tajes, C.; Rossi, D.; Schmidt, K.-H.; Simon, H.; Tassan-Got, L.; Törnqvist, H.; Vargas, J.; Voss, B.; Weick, H.; Yan, Y.

    2016-03-01

    SOFIA (Studies On Fission with Aladin) is a new experimental set-up dedicated to accurate measurement of fission-fragments isotopic yields. It is located at GSI, the only place to use inverse kinematics at relativistic energies in order to study the (γ,f) electromagnetic-induced fission. The SOFIA set-up is a large-acceptance magnetic spectrometer, which allows to fully identify both fission fragments in coincidence on the whole fission-fragment range. This paper will report on fission yields obtained in 234,235,236,238U(γ,f) reactions.

  6. U-series disequilibrium of basaltic rocks from Kick'em-Jenny submarine volcano, Lesser Antilles island arc

    NASA Astrophysics Data System (ADS)

    Huang, F.; Lundstrom, C. C.

    2005-12-01

    Kick'em Jenny (KEJ) submarine volcano located 9 km to the north of Grenada in the Lesser Antilles volcanic arc produces lavas ranging in composition from high MgO basalts to moderately evolved andesites. We have determined U-series disequilibria in 12 porphyritic lavas erupted from KEJ volcano by TIMS and MC-ICP-MS methods to constrain the timing and identify the processes creating the magma diversity observed. The SiO2 contents of samples studied here vary from 47 to 55 wt.% SiO2 while REE patterns evolve from slightly LREE enriched, MREE/HREE = 1 patterns to strongly LREE enriched, MREE depleted concave-up patterns. Separate dissolutions of sample KEJ100 indicate an external reproducibility (1s) of 0.7% for (230Th/238U) (n=4), 0.8% for (230Th/232Th) (n=4) and 0.6% for (226Ra/230Th) (n=3), respectively. For all sample, (234U/238U) lies within 0.7% of unity, suggesting that secondary alteration by seawater has not disturbed the U-series data significantly. Sample ages for these submarine erupted samples are unknown, resulting in uncertain values for initial (226Ra/230Th); however, 10 out of 12 of the measured (226Ra/230Th) range between 3.16 and 1.13 and are thus unequivocally young with respect to decay of 230Th and 231Pa since eruption. The U (0.535 - 4.876 ppm) and Th (1.25 - 10.78 ppm) concentrations increase with SiO2 contents. (230Th/232Th) has a restricted range, varying from 0.994 to 1.093 with the exception of one sample. (230Th/238U) ranges from 0.684 to 0.875 while (231Pa/235U) ranges from 1.76 up to 2.84, among the highest 231Pa excess in island arcs yet reported. These data confirm previous observations of the unusual behavior of KEJ lavas relative to global observations in having both large 238U and 231Pa excesses. Combined with (226Ra/230Th), these disequilibria observations require that 238U excesses reflect more than solely fluid addition to the mantle wedge from the subducted oceanic slab.

  7. Determination of (238)U, (232)Th and (40)K activity concentrations in riverbank soil along the Chao Phraya river basin in Thailand.

    PubMed

    Santawamaitre, T; Malain, D; Al-Sulaiti, H A; Bradley, D A; Matthews, M C; Regan, P H

    2014-12-01

    The activity concentrations of (238)U, (232)Th and (40)K in riverbank soil along the Chao Phraya river basin was determined through gamma-ray spectrometry measurements made using a hyper-pure germanium detector in a low background configuration. The ranges of activity concentrations of (238)U, (232)Th and (40)K were found to be 13.9 ↔ 76.8, 12.9 ↔ 142.9 and 178.4 ↔ 810.7 Bq kg(-1), respectively. The anthropogenic radionuclide, (137)Cs, was not observed in statistically significant amounts above the background level in the current study. The absorbed gamma dose rate in air at 1 m above the ground surface, the outdoor annual effective dose equivalent, the values of the radium equivalent activity and the external hazard index associated with all the soil samples in the present work were evaluated. The results indicate that the radiation hazard from primordial radionuclides in all soil samples from the area studied in this current work is not significant.

  8. Isotope ratios of (235)U/(238)U and (137)Cs/(235)U in black rain streaks on plaster wall caused by fallout of the Hiroshima atomic bomb.

    PubMed

    Shizuma, Kiyoshi; Endo, Satoru; Fujikawa, Yoko

    2012-02-01

    Radiological investigations of fallout from the atomic bomb detonated over Hiroshima city on 6 August 1945 are important to estimate doses for inhabitants. The authors have analyzed the concentrations of (137)Cs, (235)U, and (238)U in streaks of black rain caused by the atomic bomb using gamma-ray spectroscopy and the ICP-QMS method. The black rain streaks were deposited on a plaster wall of a house located 3.7 km west of the hypocenter that has been kept in the same condition as after the rainfall. Cesium-137 ((137)Cs) was detected from black streak samples. Concentration of (137)Cs in the black rain streaks is twice as high as fallout deposition on the ground in this area. A (235)U/(238)U atom ratio of 0.00887 was found, which is higher than the natural ratio, reflecting the fact that the atomic bomb "Little Boy" used enriched uranium as fuel. The ratio (137)Cs/(235)U was determined to be 0.0091, which is about eight times higher than the estimated ratio of 0.00113 based on the fission yield.

  9. Initial Design Calculations for a Detection System that will Observe Resonant Excitation of the 680 keV state in 238U

    SciTech Connect

    Pruet, J; Hagmann, C

    2007-01-26

    We present calculations and design considerations for a detection system that could be used to observe nuclear resonance fluorescence in {sup 238}U. This is intended as part of an experiment in which a nearly monochromatic beam of light incident on a thin foil of natural uranium resonantly populates the state at 680 keV in {sup 238}U. The beam of light is generated via Compton upscattering of laser light incident on a beam of relativistic electrons. This light source has excellent energy and angular resolution. In the current design study we suppose photons emitted following de-excitation of excited nuclei to be observed by a segmented array of BGO crystals. Monte Carlo calculations are used to inform estimates for the design and performance of this detector system. We find that each detector in this array should be shielded by about 2 cm of lead. The signal to background ratio for each of the BGO crystals is larger than ten. The probability that a single detector observes a resonant photon during a single pulse of the light source is near unity.

  10. Identification of new neutron-rich isotopes produced by in-flight fission of ^238U at 345 MeV/u

    NASA Astrophysics Data System (ADS)

    Ohnishi, Tetsuya; Kubo, Toshiyuki; Takeda, Hiroyuki; Fukuda, Naoki; Kameda, Daisuke; Kusaka, Kensuke; Yoshida, Atsushi; Yoshida, Koichi; Ohtake, Masao; Inabe, Naohito; Yanagisawa, Yoshiyuki; Tanaka, Kanenobu

    2009-10-01

    At RI Beam Factory (RIBF) at RIKEN Nishina Center, an in-flight radioactive isotope beam separator BigRIPS[1] was commissioned in 2007. Then we made a search for new isotopes using in-flight fission of a ^238U beam at 345 MeV/u, and observed two new palladium isotopes ^125Pd and ^126Pd.[2] In November 2008, we revisited this experiment with improved experimental conditions and better tuning of BigRIPS. The intensity of the ^238U beam was 1.6x10^9 particle/sec on average, which was about 40 times higher than in 2007. The search was performed for three Bρ settings that targeted different isotope regions. The achieved resolution of particle identification was good enough to well identify fission fragments even if some of them were not fully stripped. We observed more than 20 new isotopes with Z = 26 to 53, including ^128Pd, which demonstrated the RI-beam production power of BigRIPS at RIBF. The details of the experiment will be reported. [1]T. Kubo, Nucl. Instr. and Meth. B204, 97(2003). [2]T. Ohnishi et al, J. Phys. Soci. Jpn. 77, 083201(2008).

  11. Determination of ²²⁶Ra, ²²⁸Ra and ²¹⁰Pb in NORM products from oil and gas exploration: problems in activity underestimation due to the presence of metals and self-absorption of photons.

    PubMed

    Landsberger, S; Brabec, C; Canion, B; Hashem, J; Lu, C; Millsap, D; George, G

    2013-11-01

    Typical calibration of solid environmental samples for the determination of (226)Ra, (228)Ra and (210)Pb entails the use of standard reference materials which have a very similar matrix. However, TENORM samples from the oil and gas exploration contain unusually high amounts of calcium, strontium and barium which can severely attenuate the photons of (210)Pb and (226)Ra with their characteristic 46.1 keV and 186.2 keV gamma-rays, respectively and to some extent (228)Ra with the characteristic gamma-rays of 911.2 keV and 969.0 keV. We used neutron activation analysis to evaluate the content of TENORM for calcium, barium and strontium and then used a software program SELABS to determine the self-absorption. Our results confirm that even in Petrie containers with small dimensions the (210)Pb can be underestimated by almost by a factor of four while (226)Ra can be underestimated by 5%. The (228)Ra activities are virtually unaffected due to the higher energy gamma-rays. However, the implications for TENORM studies that employ large Marinelli containers having sample sizes between 0.25 and 1.0 L may be severely compromised by the presence of high Z elements in elevated concentrations. The usual spectral interferences on (226)Ra, (228)Ra and (210)Pb coming from other radionuclides in the (234)U, (235)U and (238)U decay chains are virtually nonexistent due the very high activity levels of (226)Ra, (228)Ra and (210)Pb in the tens of thousands of Bq/kg.

  12. Measurements of yields of fission products in the reaction of {sup 238}U with high-energy p, d and n beams

    SciTech Connect

    Nolen, J.A.; Ahmad, I.; Back, B.B.

    1995-08-01

    An experiment was performed at the Michigan State University cyclotron to determine the yields of neutron-rich fission products in the reaction of {sup 238}U with 100-MeV neutrons, 200-MeV deuterons and 200-MeV protons. Several 1-mm-thick {sup 238}U foils were irradiated for 100-second intervals sequentially for each configuration and the ten spectra were added for higher statistics. The three successive spectra, each for a 40 s period, were accumulated for each sample. Ten foils were irradiated. Successive spectra allowed us to determine approximate half-lives of the gamma peaks. Several arrangements, which were similar to the setup we plan to use in our radioactive beam proposal, were used for the production of fission products. For the high-energy neutron irradiation, U foils were placed after a 5-inch-long, 1-inch-diameter Be cylinder which stopped the 200-MeV deuteron beam generating 100-MeV neutrons. Arrangements for deuteron irradiation included direct irradiation of U foils, placing U foils after different lengths of (0.5 inch, 1.0 inch and 1.5 inch) 2-inch diameter U cylinder. Since the deuteron range in uranium is 17 mm, some of the irradiations were due to the secondary neutrons from the deuteron-induced fission of U. Similar arrangements were also used for the 200-MeV proton irradiation of the {sup 238}U foils. In all cases, several neutron-rich fission products were identified and their yields determined. In particular, we were able to observe Sn in all the runs and determine its yield. The data show that with our proposed radioactive device we will be able to produce more than 10{sup 12} {sup 132}Sn atoms per second in the target. Assuming an overall efficiency of 1 %, we will be able to deliver one particle nanoampere of {sup 132}Sn beam at a target location. Detailed analysis of the {gamma}-ray spectra is in progress.

  13. Trajectoires de moindre action et temps de vie pour trois modes de désintégration du noyau ^{234}U

    NASA Astrophysics Data System (ADS)

    Benfoughal, T.; Mirea, M.

    1996-10-01

    A numerical method is used to obtain the optimum cold fission paths for three decay modes of ^{234}U. The WKB-integral is minimized with respect the necking and the elongation. A term which takes into account the effect of the diffuse surface is added to the deformation energy in the framework of the macroscopic model of binary system with different charge densities. The effective masses are computed with more correct coordinates of deformation in order to include the variations of the asymmetry during the processes. Calculations are performed to obtain the fission trajectories in a large range of mass-asymmetry including cold fission, cluster emission and alpha-decay. Estimations of T_{1/2} are reported. Les trajectoires optimales de fission pour trois modes de désintégration du noyau ^{234}U sont obtenus à l'aide d'une méthode numérique. L'intégrale WKB est minimisée en fonction des coordonnées généralisées qui caractérisent le col et l'élongation. Un terme d'énergie qui prend en considération les effets dus à une surface diffuse du noyau est ajouté à l'énergie de déformation calculée dans le cadre du modèle macroscopique des systèmes binaires avec différentes densités de charge. Les masses effectives sont calculées avec des coordonnées généralisées choisis pour inclure les variations de l'asymétrie durant le processus nucléaire. Des calculs ont été effectués por obtenir les trajectoires de fission dans un grand domaine d'asymétrie de masse rendant compte de la fission froide, de l'émission spontanée de noyaux lourds et de la désintégration alpha. Des estimations de temps de vie sont reproduites.

  14. Identification of 45 New Neutron-Rich Isotopes Produced by In-Flight Fission of a 238U Beam at 345 MeV/nucleon

    NASA Astrophysics Data System (ADS)

    Tetsuya Ohnishi,; Toshiyuki Kubo,; Kensuke Kusaka,; Atsushi Yoshida,; Koichi Yoshida,; Masao Ohtake,; Naoki Fukuda,; Hiroyuki Takeda,; Daisuke Kameda,; Kanenobu Tanaka,; Naohito Inabe,; Yoshiyuki Yanagisawa,; Yasuyuki Gono,; Hiroshi Watanabe,; Hideaki Otsu,; Hidetada Baba,; Takashi Ichihara,; Yoshitaka Yamaguchi,; Maya Takechi,; Shunji Nishimura,; Hideki Ueno,; Akihiro Yoshimi,; Hiroyoshi Sakurai,; Tohru Motobayashi,; Taro Nakao,; Yutaka Mizoi,; Masafumi Matsushita,; Kazuo Ieki,; Nobuyuki Kobayashi,; Kana Tanaka,; Yosuke Kawada,; Naoki Tanaka,; Shigeki Deguchi,; Yoshiteru Satou,; Yosuke Kondo,; Takashi Nakamura,; Kenta Yoshinaga,; Chihiro Ishii,; Hideakira Yoshii,; Yuki Miyashita,; Nobuya Uematsu,; Yasutsugu Shiraki,; Toshiyuki Sumikama,; Junsei Chiba,; Eiji Ideguchi,; Akito Saito,; Takayuki Yamaguchi,; Isao Hachiuma,; Takeshi Suzuki,; Tetsuaki Moriguchi,; Akira Ozawa,; Takashi Ohtsubo,; Michael A. Famiano,; Hans Geissel,; Anthony S. Nettleton,; Oleg B. Tarasov,; Daniel P. Bazin,; Bradley M. Sherrill,; Shashikant L. Manikonda,; Jerry A. Nolen,

    2010-07-01

    A search for new isotopes using in-flight fission of a 345 MeV/nucleon 238U beam has been carried out at the RI Beam Factory at the RIKEN Nishina Center. Fission fragments were analyzed and identified by using the superconducting in-flight separator BigRIPS. We observed 45 new neutron-rich isotopes: 71Mn, 73,74Fe, 76Co, 79Ni, 81,82Cu, 84,85Zn, 87Ga, 90Ge, 95Se, 98Br, 101Kr, 103Rb, 106,107Sr, 108,109Y, 111,112Zr, 114,115Nb, 115,116,117Mo, 119,120Tc, 121,122,123,124Ru, 123,124,125,126Rh, 127,128Pd, 133Cd, 138Sn, 140Sb, 143Te, 145I, 148Xe, and 152Ba.

  15. Quantification of Uncertainties due to 235,238U, 239,240,241Pu and Fission Products Nuclear Data Uncertainties for a PWR Fuel Assembly

    NASA Astrophysics Data System (ADS)

    da Cruz, D. F.; Rochman, D.; Koning, A. J.

    2014-04-01

    Uncertainty analysis on reactivity and discharged inventory for a typical PWR fuel element as a result of uncertainties in 235,238U, 239,240,241Pu, and fission products nuclear data was performed. The Total Monte-Carlo (TMC) method was applied using the deterministic transport code DRAGON. The nuclear data used in this study is from the JEFF-3.1 evaluations, with the exception of the nuclear data files for U, Pu and fission products isotopes, which are taken from the nuclear data library TENDL-2012. Results show that the calculated total uncertainty in keff (as result of uncertainties in nuclear data of the considered isotopes) is virtually independent on fuel burnp and amounts to 700 pcm. The uncertainties in inventory of the discharged fuel is dependent on the element considered and lies in the range 1-15% for most fission products, and is below 5% for the most important actinides.

  16. Production of new neutron-rich isotopes of heavy elements in fragmentation reactions of {sup 238}U projectiles at 1A GeV

    SciTech Connect

    Alvarez-Pol, H.; Benlliure, J.; Casarejos, E.; Cortina-Gil, D.; Fernandez-Dominguez, B.; Pereira, J.; Audouin, L.; Enqvist, T.; Schmidt, K.-H.; Yordanov, O.; Junghans, A. R.; Jurado, B.; Rejmund, F.

    2010-10-15

    The production of heavy neutron-rich nuclei has been investigated using cold-fragmentation reactions of {sup 238}U projectiles at relativistic energies. The experiment performed at the high-resolving-power magnetic spectrometer Fragment Separator at GSI made it possible to identify 40 new heavy neutron-rich nuclei: {sup 205}Pt, {sup 207-210}Au, {sup 211-216}Hg, {sup 214-217}Tl, {sup 215-220}Pb, {sup 219-224}Bi, {sup 223-227}Po, {sup 225-229}At, {sup 230,231}Rn, and {sup 233}Fr. The production cross sections of these nuclei were also determined and used to benchmark reaction codes that predict the production of nuclei far from stability.

  17. (238)U/(235)U isotope ratios of crustal material, rivers and products of hydrothermal alteration: new insights on the oceanic U isotope mass balance.

    PubMed

    Noordmann, Janine; Weyer, Stefan; Georg, R Bastian; Jöns, Svenja; Sharma, Mukul

    2016-01-01

    In this study, the U isotope composition, n((238)U)/n((235)U), of major components of the upper continental crust, including granitic rocks of different age and post-Archaean shales, as well as that of rivers (the major U source to the oceans) was investigated. Furthermore, U isotope fractionation during the removal of U at mid-ocean ridges, an important sink for U from the oceans, was investigated by the analyses of hydrothermal water samples (including low- and high-temperature fluids), low-temperature altered basalts and calcium carbonate veins. All analysed rock samples from the continental crust fall into a limited range of δ(238)U between -0.45 and -0.21 ‰ (relative to NBL CRM 112-A), with an average of -0.30 ± 0.15 ‰ (2 SD, N = 11). Despite differences in catchment lithologies, all major rivers define a relatively narrow range between -0.31 and -0.13 ‰, with a weighted mean isotope composition of -0.27 ‰, which is indistinguishable from the estimate for the upper continental crust (-0.30 ‰). Only some tributary rivers from the Swiss Alps display a slightly larger range in δ(238)U (-0.29 to +0.01 ‰) and lower U concentrations (0.87-3.08 nmol/kg) compared to the investigated major rivers (5.19-11.69 nmol/kg). These findings indicate that only minor net U isotope fractionation occurs during weathering and transport of material from the continental crust to the oceans. Altered basalts display moderately enriched U concentrations (by a factor of 3-18) compared to those typically observed for normal mid-ocean ridge basalts. These, and carbonate veins within altered basalts, show large U isotope fractionation towards both heavy and light U isotope compositions (ranging from -0.63 to +0.27 ‰). Hydrothermal water samples display low U concentrations (0.3-1 nmol/kg) and only limited variations in their U isotope composition (-0.43 ± 0.25 ‰) around the seawater value. Nevertheless, two of the investigated fluids display

  18. Physical characteristics of LWRs and SCLWRs loaded by ({sup 233}U-Th-{sup 238}U) oxide fuel with small additions of {sup 231}Pa

    SciTech Connect

    Kulikov, E.G.; Shmelev, A.N.; Apse, V.A.; Kulikov, G.G.

    2007-07-01

    The paper investigates the possibility and attractiveness of using (U-Th) fuel in light-water reactors (LWRs) and in light-water reactors with super-critical coolant parameters (SCLWRs). It is proposed to dilute {sup 233}U with {sup 238}U to enhance the proliferation resistance of this fissionable isotope. If is noteworthy that she idea was put forward for the first time by she well known American physicist and participant of the Manhattan Project Dr. T. Taylor. Various fuel compositions are analyzed and compared on fuel breeding, achievable values of fuel burn-up and cross-sections of parasitic neutron absorption. It is also demonstrated that small {sup 231}Pa additions (several percent) into the fuel allows: to increase fuel burn-up, to achieve more negative temperature reactivity coefficient of coolant and to enhance nonproliferation of the fuel. (authors)

  19. High-accuracy determination of the 238U/235U fission cross section ratio up to ≈1 GeV at n_TOF at CERN

    NASA Astrophysics Data System (ADS)

    Paradela, C.; Calviani, M.; Tarrío, D.; Leal-Cidoncha, E.; Leong, L. S.; Tassan-Got, L.; Le Naour, C.; Duran, I.; Colonna, N.; Audouin, L.; Mastromarco, M.; Lo Meo, S.; Ventura, A.; Aerts, G.; Altstadt, S.; Álvarez, H.; Álvarez-Velarde, F.; Andriamonje, S.; Andrzejewski, J.; Badurek, G.; Barbagallo, M.; Baumann, P.; Bécares, V.; Bečvář, F.; Belloni, F.; Berthier, B.; Berthoumieux, E.; Billowes, J.; Boccone, V.; Bosnar, D.; Brugger, M.; Calviño, F.; Cano-Ott, D.; Capote, R.; Carrapiço, C.; Cennini, P.; Cerutti, F.; Chiaveri, E.; Chin, M.; Cortés, G.; Cortés-Giraldo, M. A.; Cosentino, L.; Couture, A.; Cox, J.; David, S.; Diakaki, M.; Dillmann, I.; Domingo-Pardo, C.; Dressler, R.; Dridi, W.; Eleftheriadis, C.; Embid-Segura, M.; Ferrant, L.; Ferrari, A.; Finocchiaro, P.; Fraval, K.; Fujii, K.; Furman, W.; Ganesan, S.; García, A. R.; Giubrone, G.; Gómez-Hornillos, M. B.; Gonçalves, I. F.; González-Romero, E.; Goverdovski, A.; Gramegna, F.; Griesmayer, E.; Guerrero, C.; Gunsing, F.; Gurusamy, P.; Haight, R.; Heil, M.; Heinitz, S.; Igashira, M.; Isaev, S.; Jenkins, D. G.; Jericha, E.; Kadi, Y.; Käppeler, F.; Karadimos, D.; Karamanis, D.; Kerveno, M.; Ketlerov, V.; Kivel, N.; Kokkoris, M.; Konovalov, V.; Krtička, M.; Kroll, J.; Lampoudis, C.; Langer, C.; Lederer, C.; Leeb, H.; Losito, R.; Lozano, M.; Manousos, A.; Marganiec, J.; Martínez, T.; Marrone, S.; Massimi, C.; Mastinu, P.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mingrone, F.; Mirea, M.; Mondelaers, W.; Moreau, C.; Mosconi, M.; Musumarra, A.; O'Brien, S.; Pancin, J.; Patronis, N.; Pavlik, A.; Pavlopoulos, P.; Perkowski, J.; Perrot, L.; Pigni, M. T.; Plag, R.; Plompen, A.; Plukis, L.; Poch, A.; Pretel, C.; Praena, J.; Quesada, J.; Rauscher, T.; Reifarth, R.; Riego, A.; Roman, F.; Rudolf, G.; Rubbia, C.; Rullhusen, P.; Salgado, J.; Santos, C.; Sarchiapone, L.; Sarmento, R.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Stephan, C.; Tagliente, G.; Tain, J. L.; Tavora, L.; Terlizzi, R.; Tsinganis, A.; Valenta, S.; Vannini, G.; Variale, V.; Vaz, P.; Versaci, R.; Vermeulen, M. J.; Villamarin, D.; Vincente, M. C.; Vlachoudis, V.; Vlastou, R.; Voss, F.; Wallner, A.; Walter, S.; Ware, T.; Weigand, M.; Weiß, C.; Wiesher, M.; Wisshak, K.; Wright, T.; Žugec, P.; n TOF Collaboration

    2015-02-01

    The 238U to 235U fission cross section ratio has been determined at n_TOF up to ≈1 GeV, with two different detection systems, in different geometrical configurations. A total of four datasets has been collected and compared. They are all consistent to each other within the relative systematic uncertainty of 3-4%. The data collected at n_TOF have been suitably combined to yield a unique fission cross section ratio as a function of neutron energy. The result confirms current evaluations up to 200 MeV. Good agreement is also observed with theoretical calculations based on the INCL ++/ Gemini++ combination up to the highest measured energy. The n_TOF results may help solve a long-standing discrepancy between the two most important experimental datasets available so far above 20 MeV, while extending the neutron energy range for the first time up to ≈1 GeV.

  20. Radioactivity In Marine Organisms From Northeast Atlantic Ocean

    SciTech Connect

    Carvalho, Fernando P.; Oliveira, Joao M.

    2008-08-07

    Naturally-occurring radionuclides such as {sup 238}U, {sup 234}U, {sup 230}Th, {sup 226}Ra, {sup 210}Po, {sup 210}Pb and {sup 232}Th, and artificial radionuclides such as {sup 137}Cs, {sup 239+240}Pu and {sup 241}Am, were measured in a large number of marine species. In common fish species, typical concentrations of {sup 210}Po ranged from 10{sup 2} to 10{sup 4} mBq kg{sup -1} (wet weight), {sup 226}Ra concentrations ranged from 1x10{sup 2} to 5xl0{sup 2} mBq kg{sup -1}, {sup 238}U was at about 10 mBq kg{sup -1} and {sup 232}Th at about 0.5 mBq kg{sup -1}. Radiation doses to marine organisms originated by naturally-occurring and artificial radionuclides accumulated in tissues and by external radiation sources were computed and compared. Internal sources generally give higher contribution to the absorbed radiation dose than external sources. Amongst radionuclides accumulated in fish muscle and acting as internal radiation sources, natural {sup 210}Po and {sup 40}K give the largest contribution to the absorbed radiation dose, while artificial radionuclides such as {sup 137}Cs and {sup 239+240}Pu contribute with less than 0.5% to the absorbed radiation dose from all internal sources.

  1. Early diagenesis impact on precise U-series dating of deep-sea corals: Example of a 100 200-year old Lophelia pertusa sample from the northeast Atlantic

    NASA Astrophysics Data System (ADS)

    Pons-Branchu, Edwige; Hillaire-Marcel, Claude; Deschamps, Pierre; Ghaleb, Bassam; Sinclair, Daniel J.

    2005-10-01

    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

  2. Influence of a Decaying Cyclonic Eddy on Biogenic Silica and Particulate Organic Carbon in the Tropical South China Sea Based on 234Th-238U Disequilibrium

    PubMed Central

    Yang, Weifeng; Chen, Min; Zheng, Minfang; He, Zhigang; Zhang, Xinxing; Qiu, Yusheng; Xu, Wangbin; Ma, Lili; Lin, Zhiyu; Hu, Wangjiang; Zeng, Jian

    2015-01-01

    Eddies play a critical role in regulating the biological pump by pumping new nutrients to the euphotic zone. However, the effects of cyclonic eddies on particle export are not well understood. Here, biogenic silica (BSi) and particulate organic carbon (POC) exports were examined inside and outside a decaying cyclonic eddy using 234Th-238U disequilibria in the tropical South China Sea. For the eddy and outside stations, the average concentrations of BSi in the euphotic zone were 0.17±0.09 μmol L-1 (mean±sd, n = 20) and 0.21±0.06 μmol L-1 (n = 34). The POC concentrations were 1.42±0.56 μmol L-1 (n = 34) and 1.30±0.46 μmol L-1 (n = 51). Both BSi and POC abundances did not show change at the 95% confidence level. Based on the 234Th-238U model, BSi export fluxes in the eddy averaged 0.18±0.15 mmol Si m-2 d-1, which was comparable with the 0.40±0.20 mmol Si m-2 d-1 outside the eddy. Similarly, the average POC export fluxes were 1.5±1.4 mmol C m-2 d-1 and 1.9±1.3 mmol C m-2 d-1 for the eddy and outside stations. From these results we concluded that cyclonic eddies in their decaying phase have little effect on the abundance and export of biogenic particles. PMID:26317555

  3. Influence of a Decaying Cyclonic Eddy on Biogenic Silica and Particulate Organic Carbon in the Tropical South China Sea Based on 234Th-238U Disequilibrium.

    PubMed

    Yang, Weifeng; Chen, Min; Zheng, Minfang; He, Zhigang; Zhang, Xinxing; Qiu, Yusheng; Xu, Wangbin; Ma, Lili; Lin, Zhiyu; Hu, Wangjiang; Zeng, Jian

    2015-01-01

    Eddies play a critical role in regulating the biological pump by pumping new nutrients to the euphotic zone. However, the effects of cyclonic eddies on particle export are not well understood. Here, biogenic silica (BSi) and particulate organic carbon (POC) exports were examined inside and outside a decaying cyclonic eddy using 234Th-238U disequilibria in the tropical South China Sea. For the eddy and outside stations, the average concentrations of BSi in the euphotic zone were 0.17±0.09 μmol L-1 (mean±sd, n = 20) and 0.21±0.06 μmol L-1 (n = 34). The POC concentrations were 1.42±0.56 μmol L-1 (n = 34) and 1.30±0.46 μmol L-1 (n = 51). Both BSi and POC abundances did not show change at the 95% confidence level. Based on the 234Th-238U model, BSi export fluxes in the eddy averaged 0.18±0.15 mmol Si m-2 d-1, which was comparable with the 0.40±0.20 mmol Si m-2 d-1 outside the eddy. Similarly, the average POC export fluxes were 1.5±1.4 mmol C m-2 d-1 and 1.9±1.3 mmol C m-2 d-1 for the eddy and outside stations. From these results we concluded that cyclonic eddies in their decaying phase have little effect on the abundance and export of biogenic particles.

  4. Feasibility of Colliding-beam fast-fission reactor via 238U80++238 U80+ --> 4 FF + 5n + 430 MeV beam with suppressed plutonium and direct conversion of fission fragment (FF) energy into electricity and/or Rocket propellant with high specific impulse

    NASA Astrophysics Data System (ADS)

    Maglich, Bogdan; Hester, Tim; Calsec Collaboration

    2015-10-01

    Uranium-uranium colliding beam experiment1, used fully ionized 238U92+ at energy 100GeV --> <-- 100 GeV, has measured total σ = 487 b. Reaction rate of colliding beams is proportional to neutron flux-squared. First functional Auto-Collider3-6, a compact Migma IV, 1 m in diameter, had self-colliding deuterons, D+, of 725 KeV --> <-- 725 KeV, resulting in copious production of T and 3He. U +U Autocollider``EXYDER'' will use strong-focusing magnet7, which would increase reaction rate by 104. 80 times ionized U ions accelerated through 3 MV accelerator, will collide beam 240 MeV --> <-- 240 MeV. Reaction is: 238U80+ +238 U80+ --> 4 FF + 5n + 430 MeV. Using a simple model1 fission σf ~ 100 b. Suppression of Pu by a factor of 106 will be achieved because NO thermal neutron fission can take place; only fast, 1-3 MeV, where σabs is negligible. Direct conversion of 95% of 430 MeV produced is carried by electrically charged FFs which are magnetically funneled for direct conversion of energy of FFs via electrostatic decelerators4,11. 90% of 930 MeV is electrically recoverable. Depending on the assumptions, we project electric _ power density production of 20 to 200 MWe m-3, equivalent to Thermal 1.3 - 13 GWthm-3. If one-half of unburned U is used for propulsion while rest powers system, heavy FF ion mass provides specific impulse Isp = 106 sec., 103 times higher than current rocket engines.

  5. Transfer Rates of 238U and 232Th for E. globulus, A. mearnsii, H. filipendula and Hazardous Effects of the Usage of Medicinal Plants From Around Gold Mine Dump Environs

    PubMed Central

    Tshivhase, Victor M.; Njinga, Raymond L.; Mathuthu, Manny; Dlamini, Thulani C.

    2015-01-01

    Medicinal plant consumption can be a source of human exposure to radioactive elements such as 238U and 232Th, which can lead to internal radiation doses. The uptake of 238U and 232Th from soils to the leaf samples of three different medicinal plant species (Eucalyptus globulus, Acacia mearnsii and Hyparrhenia filipendula) from the purlieu of the Princess gold mine dump, an abandoned contaminated tailings storage site (TSS), located at longitude 27°55′00″E and latitude 26°09′30″S in Davidsonville (Roodepoort, west of Johannesburg, South Africa) was measured. This was done using ICP-MS spectrometry and substantial differences were observed in the soil-plant transfer factor (TF) values between these radionuclides. The plant species E. globulus exhibited the highest uptake of 238U, with an average TF of 3.97, while that of H. filipendula was 0.01 and the lowest TF of 0.15 × 10−2 was measured for A. mearnsii. However, in the case of 232Th, the highest average TF was observed for A. mearnsii (0.29), followed by E. globulus (0.10) and lowest was measured for H. filipendula (0.27 × 10−2). The ratio of TF average value i.e., 238U to 232Th in the soil-plant leaves was 38.05 for E. globulus, 0.01 for A. mearnsii and 4.38 for H. filipendula. PMID:26690462

  6. The 238U/235U isotope ratio of the Earth and the solar system: Constrains from a gravimetrically calibrated U double spike and implications for absolute Pb-Pb ages

    NASA Astrophysics Data System (ADS)

    Weyer, Stefan; Noordmann, Janine; Brennecka, Greg; Richter, Stephan

    2010-05-01

    The ratio of 238U and 235U, the two primordial U isotopes, has been assumed to be constant on Earth and in the solar system. The commonly accepted value for the 238U/235U ratio, which has been used in Pb-Pb dating for the last ~ 30 years, was 137.88. Within the last few years, it has been shown that 1) there are considerable U isotope variations (~1.3‰) within terrestrial material produced by isotope fractionation during chemical reactions [1-3] and 2) there are even larger isotope variations (at least 3.5‰) in calcium-aluminum-rich inclusions (CAIs) in meoteorites that define the currently accepted age of the solar system [4]. These findings are dramatic for geochronology, as a known 238U/235U is a requirement for Pb-Pb dating, the most precise dating technique for absolute ages. As 238U/235U variations can greatly affect the reported absolute Pb-Pb age, understanding and accurately measuring variation of the 238U/235U ratio in various materials is critical, With these new findings, the questions also arises of "How well do we know the average U isotope composition of the Earth and the solar system?" and "How accurate can absolute Pb-Pb ages be?" Our results using a gravimetrically calibrated 233U/236U double spike IRMM 3636 [5] indicate that the U standard NBL 950a, which was commonly used to define the excepted "natural" 238U/235U isotope ratio, has a slightly lower 238U/235U of 137.836 ± 0.024. This value is indistinguishable from the U isotope compositions for NBL 960 and NBL112A, which have been determined by several laboratories, also using the newly calibrated U double spike IRMM 3636 [6]. These findings provide new implications about the average U isotope composition of the Earth and the solar system. Basalts display a very tight range of U isotope variations (~0.25-0.32‰ relative to SRM 950a). Their U isotope composition is also very similar to that of chondrites [4], which however appear to show a slightly larger spread. Accepting terrestrial

  7. Certified Reference Material IAEA-446 for radionuclides in Baltic Sea seaweed.

    PubMed

    Pham, M K; Benmansour, M; Carvalho, F P; Chamizo, E; Degering, D; Engeler, C; Gascó, C; Gwynn, J P; Harms, A V; Hrnecek, E; Ibanez, F L; Ilchmann, C; Ikaheimonen, T; Kanisch, G; Kloster, M; Llaurado, M; Mauring, A; Møller, B; Morimoto, T; Nielsen, S P; Nies, H; Norrlid, L D R; Pettersson, H B L; Povinec, P P; Rieth, U; Samuelsson, C; Schikowski, J; Silobritiene, B V; Smedley, P A; Suplinska, M; Vartti, V-P; Vasileva, E; Wong, J; Zalewska, T; Zhou, W

    2014-05-01

    A Certified Reference Material (CRM) for radionuclides in seaweed (Fucus vesiculosus) from the Baltic Sea (IAEA-446) is described and the results of the certification process are presented. The (40)K, (137)Cs, (234)U and (239+240)Pu radionuclides were certified for this material, and information values for 12 other radionuclides ((90)Sr, (99)Tc, (210)Pb ((210)Po), (226)Ra, (228)Ra, (228)Th, (230)Th, (232)Th, (235)U, (238)U, (239)Pu and (240)Pu) are presented. The CRM can be used for Quality Assurance/Quality Control of analysis of radionuclides in seaweed and other biota samples, as well as for development and validation of analytical methods, and for training purposes.

  8. Estimated dose to man from uranium milling via the beef/milk food-chain pathway.

    PubMed

    Rayno, D R

    1983-12-01

    One of the major pathways of radiological exposure to man from uranium milling operations is through the beef/milk food chain. Studies by various investigators have shown the extent of uptake and distribution of 238U, 234U, 230Th, 226Ra, 210Pb, and 210Po in plants and cattle. These long-lived natural radioisotopes, all nuclides of the uranium decay series, are found in concentrated amounts in uranium mill tailings. In this paper, data from these investigations are used to estimate the dose to man from consumption of beef and milk from cattle that have fed on forage contaminated with the tailings. The estimated doses from this technologically enhanced source are compared with those resulting from average dietary intake of these radionuclides from natural sources.

  9. Environmental isotopes as a useful tool for studies at mixed uranium mill tailings sites.

    PubMed

    Helling, C

    2000-01-01

    Groundwaters in the area of a mixed landfill (domestic waste above uranium mill tailings) in Dresden (Saxony, Germany) were investigated for their isotope signatures to distinguish between different groundwater types. To determine between the two contamination sources (waste and uranium mill tailings) a multi parameter interpretation was done using both, the main hydrochemical parameters the radionuclides 234U, 238U, 226Ra and 222Rn as well as the environmental isotopes of the elements hydrogen, oxygen, sulphur and carbon. The seepage water from the landfill shows higher delta34S, delta18O and tritium values as the inflow. The tritium values give an idea about water movement in the dump and mean residence time of the groundwater. The water in the dump shows varying delta13C values which indicate different processes occurring in the dump.

  10. Concentrations of U and Po in animal feed supplements, in poultry meat and in eggs

    SciTech Connect

    Izak-Biran, T.; Schlesinger, T.; Weingarten, R.; Even, O.; Shamai, Y.; Israeli, M.

    1989-03-01

    The present study was undertaken to assess the contribution of phosphate feed supplements to the radiation exposure of the population in Israel. The phosphates usually contain appreciable quantities of U and its daughters and the actual exposure of human consumers depends, to a very large extent, on the degree of equilibrium of the decay chain in the feed and through the metabolic process. The concentrations of /sup 238/U, /sup 234/U, /sup 226/Ra and /sup 210/Po (/sup 210/Pb) in poultry feed supplements and in chicken meat (breasts, thighs) and organs (livers, spleens, gizzards) as well as in eggs were determined. From the results, the transfer coefficients of U and Po in chicken meat and in eggs were calculated. The effective dose equivalent to the Israeli population due to the consumption of poultry products which accounts for approximately 70% of all meat consumed in Israel is assessed to be 0.04 mSv y-1.

  11. IAEA-447: a new certified reference material for environmental radioactivity measurements.

    PubMed

    Shakhashiro, A; Tarjan, S; Ceccatelli, A; Kis-Benedek, G; Betti, M

    2012-08-01

    The environment program of the International Atomic Energy Agency (IAEA) includes activities to produce and certify reference materials for environmental radioactivity measurements. This paper describes methodologies applied in preparation and certification of the new IAEA-447 moss-soil certified reference material. In this work, the massic activities and associated standard uncertainties of (40)K, (90)Sr, (137)Cs, (208)Tl, (210)Pb, (210)Po, (212)Pb, (214)Pb, (214)Bi, (226)Ra, (228)Ac, (234)Th, (234)U, (238)U, (238)Pu, (239+240)Pu, (241)Pu and (241)Am were established. Details of the analytical methods including radiochemical procedures were reported. Analytical challenges and lessons learned from the reported results in the worldwide IAEA proficiency test using this material was summarized and best analytical practices to improve the performance for environmental radioactivity determinations were recommended. IAEA-447 is an important reference material for quality control and method validation of gamma-ray spectrometry and radiochemical analytical procedures.

  12. A database of radionuclide activity and metal concentrations for the Alligator Rivers Region uranium province.

    PubMed

    Doering, Che; Bollhöfer, Andreas

    2016-10-01

    This paper presents a database of radionuclide activity and metal concentrations for the Alligator Rivers Region (ARR) uranium province in the Australian wet-dry tropics. The database contains 5060 sample records and 57,473 concentration values. The data are for animal, plant, soil, sediment and water samples collected by the Environmental Research Institute of the Supervising Scientist (ERISS) as part of its statutory role to undertake research and monitoring into the impacts of uranium mining on the environment of the ARR. Concentration values are provided in the database for 11 radionuclides ((227)Ac, (40)K, (210)Pb, (210)Po, (226)Ra, (228)Ra, (228)Th, (230)Th, (232)Th, (234)U, (238)U) and 26 metals (Al, As, Ba, Ca, Cd, Co, Cr, Cu, Fe, Hg, K, Mg, Mn, Na, Ni, P, Pb, Rb, S, Sb, Se, Sr, Th, U, V, Zn). Potential uses of the database are discussed.

  13. Uranium-series dating of actinide decay series mobility at Pena Blanca

    SciTech Connect

    Dixon, P.R.; Goldstein, S.J.; Murrell, M.T.

    1997-12-31

    Studies of U-series disequilibria near uranium ore deposits can provide valuable information on the mobility of actinides and their daughters over the range of timescales needed to assess the stability of proposed waste repositories. We have applied highly sensitive TIMS methods to obtain 238U-234U-230Th dates for three whole rock samples within a {approximately}30 in long fracture emanating into surrounding tuff from the deposit at Pena Blanca, Mexico. The 238U-234U-230Th data lie on a whole-rock isochron that requires closed-system behavior for the last 380 ka. Preliminary 231Pa-235U data for the U-rich vein also indicates closed system behavior for at least the last 100 ka. In contrast, 226Ra/230Th activity ratios range from 0.76-0.99 which indicates more recent Ra mobility within the fracture most likely due to surface water infiltration. Our results require uranium, thorium and protactinium stability despite recent radium mobility and provide important constraints on repository stability over {approximately}100 ka timescales.

  14. Identification of 45 new neutron-rich isotopes produced by in-flight fission of a {sup 238}U beam at 345 MeV/nucleon.

    SciTech Connect

    Ohnishi, T.; Kubo, T.; Kusaka, K.; Yoshida, A.; Yoshida, K.; Manikonda, S.; Nolen, J.

    2010-07-12

    A search for new isotopes using in-flight fission of a 345 MeV/nucleon {sup 238}U beam has been carried out at the RI Beam Factory at the RIKEN Nishina Center. Fission fragments were analyzed and identified by using the superconducting in-flight separator BigRIPS. We observed 45 new neutron-rich isotopes: {sup 71}Mn, {sup 73,74}Fe, {sup 76}Co, {sup 79}Ni, {sup 81,82}Cu, {sup 84,85}Zn, {sup 87}Ga, {sup 90}Ge, {sup 95}Se, {sup 98}Br, {sup 101}Kr, {sup 103}Rb, {sup 106,107}Sr, {sup 108,109}Y, {sup 111,112}Zr, {sup 114,115}Nb, {sup 115,116,117}Mo, {sup 119,120}Tc, {sup 121,122,123,124}Ru, {sup 123,124,125,126}Rh, {sup 127,128}Pd, {sup 133}Cd, {sup 138}Sn, {sup 140}Sb, {sup 143}Te, {sup 145}I, {sup 148}Xe, and {sup 152}Ba.

  15. R-Matrix Analysis of 238U High Resolution Neutron Transmissions and Capture Cross Sections in the Energy Range 0 keV to 20 keV

    SciTech Connect

    Derrien, Herve; Leal, Luiz C; Larson, Nancy M

    2009-01-01

    The neutron resonance parameters of 238U were obtained from a SAMMY analysis of high-resolution neutron transmission measurements and high-resolution capture cross section measurements performed at the Oak Ridge Electron Linear Accelerator (ORELA) in the years 1970-1990 and from more recent transmission and capture cross section measurements performed at the Geel Linear Accelerator (GELINA). Compared with previous evaluations, the energy range for this resonance analysis was extended from 10 to 20 keV, taking advantage of the high resolution of the most recent ORELA transmission measurements. The experimental database and the method of analysis are described in this report. The neutron transmissions and the capture cross sections calculated with the resonance parameters are compared with the experimental data. A description is given of the statistical properties of the resonance parameters and of the recommended values of the average parameters. The new evaluation results in a slight decrease of the effective capture resonance integral and improves the prediction of integral thermal benchmarks by 70 to 200 pcm.

  16. High-resolution tephrochronology of the Wilson Creek Formation (Mono Lake, California) and Laschamp event using 238U-230Th SIMS dating of accessory mineral rims

    NASA Astrophysics Data System (ADS)

    Vazquez, Jorge A.; Lidzbarski, Marsha I.

    2012-12-01

    Sediments of the Wilson Creek Formation surrounding Mono Lake preserve a high-resolution archive of glacial and pluvial responses along the eastern Sierra Nevada due to late Pleistocene climate change. An absolute chronology for the Wilson Creek stratigraphy is critical for correlating the paleoclimate record to other archives in the western U.S. and the North Atlantic region. However, multiple attempts to date the Wilson Creek stratigraphy using carbonates and tephras yield discordant results due to open-system effects and radiocarbon reservoir uncertainties as well as abundant xenocrysts. New ion microprobe 238U-230Th dating of the final increments of crystallization recorded by allanite and zircon autocrysts from juvenile pyroclasts yield ages that effectively date eruption of key tephra beds and delimit the timing of basal Wilson Creek sedimentation to the interval between 26.8±2.1 and 61.7±1.9 ka. Tephra (Ash 15) erupted during the geomagnetic excursion originally designated the Mono Lake excursion yields an age of 40.8±1.9 ka, indicating that the event is instead the Laschamp excursion. The new ages support a depositional chronology from magnetostratigraphy that indicates quasi-synchronous glacial and hydrologic responses in the Sierra Nevada and Mono Basin to regional climate change, with intervals of lake filling and glacial-snowpack melting that are in phase with peaks in spring insolation.

  17. Synthesis of rutherfordium isotopes in the 238U(26Mg, xn)264-xRf reaction and study of their decay properties

    SciTech Connect

    Gates, Jacklyn M; Gates, J.M.; Garcia, M.A.; Gregorich, K.E.; Dullmann, Ch.E.; Dragojevic, I.; Dvorak, J.; Eichler, R.; Folden III, C.M.; Loveland, W.; Nelson, S.L.; Pang, G.K.; Stavsetra, L.; Sudowe, R.; Turler, A.; Nitsche, H.

    2008-01-15

    Isotopes of rutherfordium (258-261Rf) were produced in irradiations of 238U targets with 26Mg beams. Excitation functions were measured for the 4n, 5n and 6n exit channels. Production of 261Rf in the 3n exit channel with a cross section of 28+92-26 pb was observed. Alpha decay of 258Rf was observed for the first time with an alpha-particle energy of 9.05+-0.03 MeV and an alpha/total decay branching ratio of 0.31+-0.11. In 259Rf, the electron capture/total decay branching ratio was measured to be 0.15+-0.04. The measured half-lives for 258Rf, 259Rf and 260Rf were 14.7+1.2-1.0 ms, 2.5+0.4-0.3 s and 22.2+3.0-2.4 ms, respectively, in agreement with literature data. The systematics of the alpha decay Q values and of the partial spontaneous fission half-lives were evaluated for even-even nuclides in the region of the N = 152, Z = 100 deformed shell. The influence of the N = 152 shell on the alpha decay Q values for rutherfordium was observed to be similar to that of the lighter elements (96<_ Z<_ 102). However, the N = 152 shell does not stabilize the rutherfordium isotopes against spontaneous fission, as it does in the lighter elements (96<_ Z<_102).

  18. High-resolution tephrochronology of the Wilson Creek Formation (Mono Lake, California) and Laschamp event using 238U-230Th SIMS dating of accessory mineral rims

    USGS Publications Warehouse

    Vazquez, Jorge A.; Lidzbarski, Marsha I.

    2012-01-01

    Sediments of the Wilson Creek Formation surrounding Mono Lake preserve a high-resolution archive of glacial and pluvial responses along the eastern Sierra Nevada due to late Pleistocene climate change. An absolute chronology for the Wilson Creek stratigraphy is critical for correlating the paleoclimate record to other archives in the western U.S. and the North Atlantic region. However, multiple attempts to date the Wilson Creek stratigraphy using carbonates and tephras yield discordant results due to open-system effects and radiocarbon reservoir uncertainties as well as abundant xenocrysts. New ion microprobe 238U-230Th dating of the final increments of crystallization recorded by allanite and zircon autocrysts from juvenile pyroclasts yield ages that effectively date eruption of key tephra beds and delimit the timing of basal Wilson Creek sedimentation to the interval between 26.8±2.1 and 61.7±1.9 ka. Tephra (Ash 15) erupted during the geomagnetic excursion originally designated the Mono Lake excursion yields an age of 40.8±1.9 ka, indicating that the event is instead the Laschamp excursion. The new ages support a depositional chronology from magnetostratigraphy that indicates quasi-synchronous glacial and hydrologic responses in the Sierra Nevada and Mono Basin to regional climate change, with intervals of lake filling and glacial-snowpack melting that are in phase with peaks in spring insolation.

  19. Observation of new neutron-rich micro-second isomers among fission products of ^238U at 345 MeV/u

    NASA Astrophysics Data System (ADS)

    Kameda, Daisuke; Nakao, Taro; Kubo, Toshiyuki; Ohnishi, Tetsuya; Takeda, Hiroyuki; Fukuda, Naoki; Kusaka, Kensuke; Yoshida, Atsushi; Yoshida, Koichi; Ohtake, Masao; Inabe, Naohito; Yanagisawa, Yoshiyuki; Tanaka, Kanenobu; Gono, Yasuyuki

    2009-10-01

    In the production of the radioactive isotope (RI) beam using projectile fragment separators, γ rays emitted from metastable states, isomers, of the reaction products can be used as a fingerprint of the isotope that is analyzed in the separator. In the operation of the superconducting in-flight RI beam separator BigRIPS [1] at RIKEN RI Beam Factory, the detection of such γ rays plays important roles not only in the identification of the RI beam [2] but also in searching for new isomers, providing valuable spectroscopic information on the isotopes. In the recent new-isotope production experiment with BigRIPS using in-flight fission of 345 MeV/nucleon ^238U at the beam intensity around 0.3 pnA, we have observed a number of short-lived isomeric decays which include unknown decays from more than 10 isotopes, using three clover-type Ge detectors with a beam stopper of aluminum. The primal result of the observations will be reported. [1] T. Kubo: Nucl. Instr. and Meth. B 204 (2003) 97. [2] T. Ohnishi et al.: J. Phys. Soc. Japan, 77 (2008) 083201.

  20. Vertical and horizontal distribution of radionuclides (232Th, 238U and 40K) in sediment from Manjung coastal water area Perak, Malaysia

    NASA Astrophysics Data System (ADS)

    Abdullah, Anisa; Hamzah, Zaini; Saat, Ahmad; Wood, Ab. Khalik

    2016-01-01

    Distribution of radionuclides from anthropogenic activities has been widely studied in marine coastal area. Due to rapid population growth and socio-economic development in Manjung area such as coal fired power plant, iron foundries, port development, waste discharged from factories and agriculture runoff may contribute to increase in pollution rate. The radioactive materials from anthropogenic activities could deteriorate the quality of the marine ecosystem and thus lead to possible radiological health risk to the population. Radionuclides (232Th, 238U and 40K) content in surface and profile sediment from Manjung coastal area was determined in this study. Radionuclides in sediment from seven locations were collected using sediment core sampling and measurements were carried out using Energy Dispersive X-ray Fluorescence (EDXRF) spectroscopy. The results show that the concentration of radionuclides in surface sediment and distribution trend of depth vertical profile sediment generally varies depending on locations. Enrichment factors (EF), geo-accumulation index (Igeo) and pollution index (PI) were applied to determine level of pollution of this study area. The radiological risks related to human exposure were evaluated based on external hazard index (Hex).

  1. Vertical and horizontal distribution of radionuclides ({sup 232}Th, {sup 238}U and {sup 40}K) in sediment from Manjung coastal water area Perak, Malaysia

    SciTech Connect

    Abdullah, Anisa Hamzah, Zaini; Wood, Ab. Khalik; Saat, Ahmad

    2016-01-22

    Distribution of radionuclides from anthropogenic activities has been widely studied in marine coastal area. Due to rapid population growth and socio-economic development in Manjung area such as coal fired power plant, iron foundries, port development, waste discharged from factories and agriculture runoff may contribute to increase in pollution rate. The radioactive materials from anthropogenic activities could deteriorate the quality of the marine ecosystem and thus lead to possible radiological health risk to the population. Radionuclides ({sup 232}Th, {sup 238}U and {sup 40}K) content in surface and profile sediment from Manjung coastal area was determined in this study. Radionuclides in sediment from seven locations were collected using sediment core sampling and measurements were carried out using Energy Dispersive X-ray Fluorescence (EDXRF) spectroscopy. The results show that the concentration of radionuclides in surface sediment and distribution trend of depth vertical profile sediment generally varies depending on locations. Enrichment factors (EF), geo-accumulation index (I{sub geo}) and pollution index (PI) were applied to determine level of pollution of this study area. The radiological risks related to human exposure were evaluated based on external hazard index (H{sub ex})

  2. Energy Dependence of Neutron-Induced Fission Product Yields of 235U, 238U and 239Pu Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, Matthew; Tornow, Werner; Tonchev, Anton; Vieira, Dave; Wilhelmy, Jerry; Arnold, Charles; Fowler, Malcolm; Stoyer, Mark

    2014-09-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements have been performed. The energy dependence of a number of cumulative fission products between 0.5 and 14.8 MeV have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of activation utilizing specially designed dual-fission chambers and γ-ray counting. The dual-fission chambers are back-to-back ionization chambers encasing a target with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the fission rate in the activation target with no reference to the fission cross-section, reducing uncertainties. γ-ray counting was performed on well-shield HPGe detectors over a period of 2 months per activation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 4.6 and 14.8 MeV.

  3. Natural radioactivity in tap waters from the private wells in the surroundings of the former Žirovski Vrh uranium mine and the age-dependent dose assessment.

    PubMed

    Benedik, Ljudmila; Rovan, Leja; Klemenčič, Hiacinta; Gantar, Ivan; Prosen, Helena

    2015-08-01

    Activity concentration of (238)U, (234)U, (226)Ra, (228)Ra, (210)Pb and (210)Po in tap water from selected springs and private wells in the area of the former uranium mine at Žirovski Vrh were determined. A total of 22 tap water samples were collected at consumer's houses. The results show that the activity concentrations of uranium in water samples are in range (0.17-372) and (0.22-362) mBq L(-1) for (238)U and (234)U, respectively. Radium activity concentrations are in range (0.14-16.7) and (0.9-11.7) mBq L(-1) for (226)Ra and (228)Ra, respectively. (210)Po activity concentration is in range (0.28-8.0) mBq L(-1) and can be regarded as the lowest amongst all analysed radionuclides. The range for (210)Pb is (0.5-24.6) mBq L(-1). Based on the results obtained for activity concentrations of six radionuclides, the committed effective dose for three different age groups of population were estimated. It was found that the committed effective dose was well below the recommended value of 100 μSv year(-1), ranging from 2.3 to 34.3 μSv year(-1) for adults, from 3.5 to 32.0 μSv year(-1) for children (7-12 years) and from 3.0 to 23.3 μSv year(-1) for infants.

  4. ESR dating of tooth enamel: comparison with {230Th }/{234U } speleothem dates at La Chaise-de-Vouthon (Charente), France

    NASA Astrophysics Data System (ADS)

    Blackwell, Bonnie; Porat, N.; Schwarcz, H. P.; Debénath, A.

    One way to assess a new dating method's reliability is by comparing its results with those from well established, independent techniques. A controlled test of the electron spin resonance (ESR) dating method as it is currently being applied to teeth was attempted for the time range 100-250 ka, beyond that of 14C, at the archaeological site of La Chaise-de-Vouthon (Charente, France). Although absent in modern enamel, a single ESR signal with g = 2.0018 in fossil tooth enamel hydroxyapatite increases in amplitude with increasing irradiation doses. ESR ages are derived from the ratio of the AD, the radiation dose needed to produce the observed ESR signal, relative to the natural, environmental dose rate (ED) experienced by the tooth after deposition. Since the age depends on the uranium (U) uptake history assumed, three ages are calculated assuming: (1) early U uptake (EU); (2) continuous (linear) uptake (LU); (3) recent uptake (RU). Generally, the LU age agrees best with known ages determined by other methods, although the RU model is better for some teeth. ESR dating assumes that the fossil has not suffered recrystallization or significant diagenetic alteration. In the preliminary test, three teeth were dated. In Bourgeois-Delaunay, a bovid molar associated with Palaeolithic artefacts was collected from layers dated at 101 ± 12 to 114 ± 7 ka by {230Th }/{234U } dating of the over- and underlying stalagmitic floors. From Suard, two Equus teeth were collected from beneath a stalagmitic floor dating 112 ± 12 ka. ESR dating teeth significantly underestimated the true age for the teeth: the mean ESR ages range from 37 to 94 ka with standard errors of 2-6 ka, and good replicability. Although more teeth at La Chaise need to be tested to ascertain that the underestimation does not result from random variation commonly seen among teeth within one unit, the consistent underestimation suggests a fault in one of the assumptions underlying the dating method. The most obvious

  5. Rates of carbonate soil evolution from carbon, U- and Th-series isotope studies: Example of the Astian sands (SE France)

    NASA Astrophysics Data System (ADS)

    Barbecot, Florent; Ghaleb, Bassam; Hillaire-Marcel, Claude

    2015-04-01

    In carbonate rich soils, C-isotopes (14C, 13C) and carbonate mass budget may inform on centennial to millennial time scale dissolution/precipitation processes and weathering rates, whereas disequilibria between in the U- and Th-decay series provide tools to document high- (228Ra-228Th-210Pb) to low- (234U, 230Th, 231Pa, 226Ra) geochemical processes rate, covering annual to ~ 1Ma time scales, governing both carbonate and silicate soil fractions. Because lithology constitutes a boundary condition, we intend to illustrate the behavior of such isotopes in soils developed over Astian sands formation (up to ~ 30% carbonate) from the Béziers area (SE France). A >20 m thick unsaturated zone was sampled firstly along a naturally exposed section, then in a cored sequence. Geochemical and mineralogical analyses, including stable isotopes and 14C-measurements, were complemented with 228U, 234U, 230Th, 226Ra, 210Pb and 228Th, 232Th measurements. Whereas the upper 7 m depict geochemical and isotopic features forced by dissolution/precipitation processes leading to variable radioactive disequilibria, but overall deficits in more soluble elements of the decay series, the lower part of the sequence shows strong excesses in 234U and 230Th over parent isotopes (i.e., 238U and 234U, respectively). These features might have been interpreted as the result of successive phases of U-loss and gains. However, 226Ra and 230Th are in near-equilibrium, thus leading to conclude at a more likely slow enrichment process in both 234Th(234U) and 230Th, which we link to dissolved U-decay during groundwater recharge events. In addition, 210Pb deficits (vs parent 226Ra) are observed down to 12 m along the natural outcropping section and below the top-soil 210Pb-excess in the cored sequence, due to gaseous 222Rn-diffusion over the cliff outcrop. Based on C-isotope and chemical analysis, reaction rates at 14C-time scale are distinct from those estimates at the short- or long-lived U-series isotopes

  6. Theoretical analyses of (n,xn) reactions on sup 235 U, sup 238 U, sup 237 Np, and sup 239 Pu for ENDF/B-VI

    SciTech Connect

    Young, P.G.; Arthur, E.D.

    1991-01-01

    Theoretical analyses were performed of neutron-induced reactions on {sup 235}U, {sup 238}U, {sup 237}Np, and {sup 239}Pu between 0.01 and 20 MeV in order to calculate neutron emission cross sections and spectra for ENDF/B-VI evaluations. Coupled-channel optical model potentials were obtained for each target nucleus by fitting total, elastic, and inelastic scattering cross section data, as well as low-energy average resonance data. The resulting deformed optical model potentials were used to calculate direct (n,n{prime}) cross sections and transmission coefficients for use in Hauser-Feshbach statistical theory analyses. A fission model with multiple barrier representation, width fluctuation corrections, and preequilibrium corrections were included in the analyses. Direct cross sections for higher-lying vibrational states were calculated using DWBA theory, normalized using B(E{ell}) values determined from (d,d{prime}) and Coulomb excitation data, where available, and from systematics otherwise. Initial fission barrier parameters and transition state density enhancements appropriate to the compound systems involved were obtained from previous analyses, especially fits to charged-particle fission probability data. The parameters for the fission model were adjusted for each target system to obtain optimum agreement with direct (n,f) cross section measurements, taking account of the various multichance fission channels, that is, the different compound systems involved. The results from these analyses were used to calculate most of the neutron (n,n), (n,n{prime}), and (n,xn) cross section data in the ENDF/B/VI evaluations for the above nuclei, and all of the energy-angle correlated spectra. The deformed optical model and fission model parameterizations are described. Comparisons are given between the results of these analyses and the previous ENDF/B-V evaluations as well as with the available experimental data. 14 refs., 3 figs., 1 tab.

  7. Thallium, uranium, and {sup 235}U/{sup 238}U ratios in the digestive gland of American lobster (Homarus americanus) from an industrialized harbor

    SciTech Connect

    Chou, C.L.; Uthe, J.F.

    1995-01-01

    Only a few studies have concentrated on elements such as thallium (TI). Uranium (U) has been studied as a radionuclide of concern in food and the environment. Foodstuffs contain 10-100 ng U{center_dot}{sup -1} with vegetables and cereals contributing most heavily to the daily intake of ca 1.5 ug U. Between 10-30% of ingested U is absorbed, with most being stored in bone. Rainbow trout (onchorynchus mykiss) and longnose sucker (Catostomus catostomus) from a lake with naturally high radioactivity contained < 5 ng U{center_dot}g{sup -1} in the flesh. Trout bone contained 40 ng U{center_dot}g{sup -1}. Higher tissue U concentrations occurred in fish from areas receiving U mining wastes. Bioconcentration factors for bone and flesh were estimated to be low, 118 and 14.7, respectively. This paper describes the Inductively coupled plasma-mass spectrometry (ICP-MS) determination of Tl and U in digestive gland tissue from lobsters captured in the vicinity of Belledune Harbor, New Brunswick, Canada. The harbor is the site of a lead smelter, a fertilizer plant, and a coal-fired power station (the latter due to enter production in late 1993) and thus has the potential of adding significant amounts of Tl to the local marine environment. The accumulation of Tl from water by marine shellfish is low, at least for bivalves, and the accumulated Tl is eliminated in a number of days when the animals are transferred to clean water. Bioconcentration factors for U in finfish ranged from 0.4-17 for larger species. However, because of the high concentrations of various trace elements in lobster digestive gland, its desirability as a foodstuff, and its relatively large size (approximately 20% of the edible tissue yield), we have investigated Tl and U concentrations and {sup 235U}/{sup 238U} ratios in it. 15 refs., 1 fig., 3 tabs.

  8. Nuclear orientation in the reaction {sup 34}S+{sup 238}U and synthesis of the new isotope {sup 268}Hs

    SciTech Connect

    Nishio, K.; Ikezoe, H.; Mitsuoka, S.; Nagame, Y.; Nishinaka, I.; Hofmann, S.; Hessberger, F. P.; Ackermann, D.; Duellmann, Ch. E.; Heinz, S.; Heredia, J. A.; Khuyagbaatar, J.; Kindler, B.; Kojouharov, I.; Lommel, B.; Mann, R.; Schaedel, M.; Antalic, S.; Saro, S.; Aritomo, Y.

    2010-08-15

    The synthesis of isotopes of the element hassium was studied using the reaction {sup 34}S+{sup 238}U{yields}{sup 272}Hs{sup *}. At a kinetic energy of 163.0 MeV in the center-of-mass system we observed one {alpha}-decay chain starting at the isotope {sup 267}Hs. The cross section was 1.8{sub -1.5}{sup +4.2} pb. At 152.0 MeV one decay of the new isotope {sup 268}Hs was observed. It decays with a half-life of 0.38{sub -0.17}{sup +1.8} s by 9479{+-}16 keV {alpha}-particle emission. Spontaneous fission of the daughter nucleus {sup 264}Sg was confirmed. The measured cross section was 0.54{sub -0.45}{sup +1.3} pb. In-beam measurements of fission-fragment mass distributions were performed to obtain information on the fusion probability at various orientations of the deformed target nucleus. The distributions changed from symmetry to asymmetry when the beam energy was changed from above-barrier to sub-barrier values, indicating orientation effects on fusion and/or quasifission. It was found that the distribution of symmetric mass fragments originates not only from fusion-fission, but has a strong component from quasifission. The result was supported by a calculation based on a dynamical description using the Langevin equation, in which the mass distributions for fusion-fission and quasifission fragments were separately determined.

  9. Measurement of 238U and 232Th in Petrol, Gas-oil and Lubricant Samples by Using Nuclear Track Detectors and Resulting Radiation Doses to the Skin of Mechanic Workers.

    PubMed

    Misdaq, M A; Chaouqi, A; Ouguidi, J; Touti, R; Mortassim, A

    2015-10-01

    Workers in repair shops of vehicles (cars, buses, truck, etc.) clean carburetors, check fuel distribution, and perform oil changes and greasing. To explore the exposure pathway of (238)U and (232)Th and its decay products to the skin of mechanic workers, these radionuclides were measured inside petrol, gas-oil, and lubricant material samples by means of CR-39 and LR-115 type II solid state nuclear track detectors (SSNTDs), and corresponding annual committed equivalent doses to skin were determined. The maximum total equivalent effective dose to skin due to the (238)U and (232)Th series from the application of different petrol, gas-oil, and lubricant samples by mechanic workers was found equal to 1.2 mSv y(-1) cm(-2).

  10. Beta and gamma decay heat measurements between 0.1s--50,000s for neutron fission of {sup 235}U, {sup 238}U and {sup 239}Pu. Final report, June 1, 1992--December 31, 1996

    SciTech Connect

    Schier, W. A.; Couchell, G. P.

    1996-01-01

    This is a final reporting on the composition of separate beta and gamma decay heat measurements following neutron fission of {sup 235}U and {sup 238}U and {sup 239}Pu and on cumulative and independent yield measurements of fission products of {sup 235}U and {sup 238}U. What made these studies unique was the very short time of 0.1 s after fission that could be achieved by incorporating the helium jet and tape transport system as the technique for transporting fission fragments from the neutron environment of the fission chamber to the low-background environment of the counting area. This capability allowed for the first time decay heat measurements to extend nearly two decades lower on the logarithmic delay time scale, a region where no comprehensive aggregate decay heat measurements had extended to. This short delay time capability also allowed the measurement of individual fission products with half lives as short as 0.2s. The purpose of such studies was to provide tests both at the aggregate level and at the individual nuclide level of the nation`s evaluated nuclear data file associated with fission, ENDF/B-VI. The results of these tests are in general quite encouraging indicating this data base generally predicts correctly the aggregate beta and aggregate gamma decay heat as a function of delay time for {sup 235}U, {sup 238}U and {sup 239}Pu. Agreement with the measured individual nuclide cumulative and independent yields for fission products of {sup 235}U and {sup 238}U was also quite good although the present measurements suggest needed improvements in several individual cases.

  11. The detailed analysis of natural radionuclides dissolved in spa waters of the Kłodzko Valley, Sudety Mountains, Poland.

    PubMed

    Walencik-Łata, A; Kozłowska, B; Dorda, J; Przylibski, T A

    2016-11-01

    A survey was conducted to measure natural radioactivity in spa waters from the Kłodzko Valley. The main goal of this study was to determine the activity concentration of uranium, radium and radon isotopes in the investigated groundwaters. Samples were collected several times from 35 water intakes from 5 spas and 2 mineral water bottling plants. The authors examined whether the increased gamma radiation background, as well as the elevated values of radium and uranium content in reservoir rocks, have a significant impact on the natural radioactivity of these waters. The second objective of this research was to provide information about geochemistry of U, Ra, Rn radionuclides and the radiological and chemical risks incurred by ingestion of isotopes with drinking water. On the basis of results obtained, it is feasible to assess the health hazard posed by ingestion of natural radioactivity with drinking waters. Moreover, the data yielded by this research may be helpful in the process of verification of the application of these waters in balneotherapy. In addition, annual effective radiation doses resulting from the isotopes consumption were calculated on the basis of the evaluated activity concentrations. In dose assessment for uranium and radium isotopes, the authors provided values for different human age groups. The obtained uranium content in the investigated waters was compared with the currently valid regulations concerning the quality of drinking water. Based on the activity concentrations data, the activity isotopic ratios (234)U/(238)U, (226)Ra/(238)U, (222)Rn/(238)U, (222)Rn/(226)Ra and the correlations between radionuclides content were then examined. In brief, it may be concluded on the basis of the obtained results that radon solubility is inversely proportional to radium and uranium dissolution in environmental water circulation. The presented study allows conclusions to be drawn on the radionuclide circulation among different environmental biota: from

  12. Environmental evolution records reflected by radionuclides in the sediment of coastal wetlands: A case study in the Yellow River Estuary wetland.

    PubMed

    Wang, Qidong; Song, Jinming; Li, Xuegang; Yuan, Huamao; Li, Ning; Cao, Lei

    2016-10-01

    Vertical profiles of environmental radionuclides ((210)Pb, (137)Cs, (238)U, (232)Th, (226)Ra and (4)(0)K) in a sediment core (Y1) of the Yellow River Estuary wetland were investigated to assess whether environmental evolutions in the coastal wetland could be recorded by the distributions of radionuclides. Based on (210)Pb and (137)Cs dating, the average sedimentation rate of core Y1 was estimated to be 1.0 cm y(-1). Vertical distributions of natural radionuclides ((238)U, (232)Th, (226)Ra and (40)K) changed dramatically, reflecting great changes in sediment input. Concentrations of (238)U, (232)Th, (226)Ra and (40)K all had significant positive relationships with organic matter and clay content, but their distributions were determined by different factors. Factor analysis showed that (238)U was determined by the river sediment input while (226)Ra was mainly affected by the seawater erosion. Environmental changes such as river channel migrations and sediment discharge variations could always cause changes in the concentrations of radionuclides. High concentrations of (238)U and (226)Ra were consistent with high accretion rate. Frequent seawater intrusion decreased the concentration of (226)Ra significantly. The value of (238)U/(226)Ra tended to be higher when the sedimentation rate was low and tide intrusion was frequent. In summary, environmental evolutions in the estuary coastal wetland could be recorded by the vertical profiles of natural radionuclides.

  13. Crystallisation ages in coeval silicic magma bodies: 238U-230Th disequilibrium evidence from the Rotoiti and earthquake flat eruption deposits, Taupo volcanic zone, New Zealand

    USGS Publications Warehouse

    Charlier, B.L.A.; Peate, D.W.; Wilson, C.J.N.; Lowenstern, J. B.; Storey, M.; Brown, S.J.A.

    2003-01-01

    The timescales over which moderate to large bodies of silicic magma are generated and stored are addressed here by studies of two geographically adjacent, successive eruption deposits in the Taupo Volcanic Zone, New Zealand. The earlier, caldera-forming Rotoiti eruption (>100 km3 magma) at Okataina volcano was followed, within months at most, by the Earthquake Flat eruption (??? 10 km3 magma) from nearby Kapenga volcano; both generated nonwelded ignimbrite and coeval widespread fall deposits. The Rotoiti and Earthquake Flat deposits are both crystal-rich high-silica rhyolites, with sparse glass-bearing granitoid fragments also occurring in Rotoiti lag breccias generated during caldera collapse. Here we report 238U-230Th disequilibrium data on whole rocks and mineral separates from representative Rotoiti and Earthquake Flat pumices and the co-eruptive Rotoiti granitoid fragments using TIMS and in situ zircon analyses by SIMS. Multiple-grain zircon-controlled crystallisation ages measured by TIMS from the Rotoiti pumice range from 69??3 ka ( 350 ka, with a pronounced peak at 70-90 ka. The weighted mean of isochrons is 83??14 ka, in accord with the TIMS data. One glass-bearing Rotoiti granitoid clast yielded an age of 57??8 ka by TIMS (controlled by Th-rich phases that, however, are not apparently present in the juvenile pumices). Another glass-bearing Rotoiti granitoid yielded SIMS zircon model ages peaking at 60-90 ka, having a similar age distribution to the pumice. Age data from pumices are consistent with a published 64??4 ka eruptive age (now modified to 62??2 ka), but chemical and/or mineralogical data imply that the granitoid lithics are not largely crystalline Rotoiti rhyolite, but instead represent contemporaneous partly molten intrusions reflecting different sources in their chemistries and mineralogies. Similarly, although the Earthquake Flat eruption immediately followed (and probably was triggered by) the Rotoiti event, age data from juvenile material

  14. Discriminating assimilants and decoupling deep- vs. shallow-level crystal records at Mount Adams using 238U-230Th disequilibria and Os isotopes

    USGS Publications Warehouse

    Jicha, B.R.; Johnson, C.M.; Hildreth, W.; Beard, B.L.; Hart, G.L.; Shirey, S.B.; Singer, B.S.

    2009-01-01

    A suite of 23 basaltic to dacitic lavas erupted over the last 350??kyr from the Mount Adams volcanic field has been analyzed for U-Th isotope compositions to evaluate the roles of mantle versus crustal components during magma genesis. All of the lavas have (230Th/238U) > 1 and span a large range in (230Th/232Th) ratios, and most basalts have higher (230Th/232Th) ratios than andesites and dacites. Several of the lavas contain antecrysts (crystals of pre-existing material), yet internal U-Th mineral isochrons from six of seven lavas are indistinguishable from their eruption ages. This indicates a relatively brief period of time between crystal growth and eruption for most of the phenocrysts (olivine, clinopyroxene, plagioclase, magnetite) prior to eruption. One isochron gave a crystallization age that is ~ 20-25??ka older than its corresponding eruptive age, and is interpreted to reflect mixing of older and juvenile crystals or a protracted period of magma storage in the crust. Much of the eruptive volume since 350??ka consists of lavas that have small to moderate 230Th excesses (2-16%), which are likely inherited from melting of a garnet-bearing intraplate ("OIB-like") mantle source. Following melt generation and subsequent migration through the upper mantle, most Mt. Adams magmas interacted with young, mafic lower crust, as indicated by 187Os/188Os ratios that are substantially more radiogenic than the mantle or those expected via mixing of subducted material and the mantle wedge. Moreover, Os-Th isotope variations suggest that unusually large 230Th excesses (25-48%) and high 187Os/188Os ratios in some peripheral lavas reflect assimilation of small degree partial melts of pre-Quaternary basement that had residual garnet or Al-rich clinopyroxene. Despite the isotopic evidence for lower crustal assimilation, these processes are not generally recorded in the erupted phenocrysts, indicating that the crystal record of the deep-level 'cryptic' processes has been

  15. Eruption and magma crystallization ages of Las Tres Vírgenes (Baja California) constrained by combined 230Th/ 238U and (U-Th)/He dating of zircon

    NASA Astrophysics Data System (ADS)

    Schmitt, Axel K.; Stockli, Daniel F.; Hausback, Brian P.

    2006-11-01

    Las Tres Vírgenes volcano is a calc-alkaline composite cone located near the main Gulf of California escarpment on the E coast of the Baja California peninsula. High-sensitivity ion microprobe U-series ( 230Th/ 238U) ages for zircon from La Vírgen tephra average 121 - 10 + 12 ka (1σ; MSWD = 2.7), with discrete age peaks at ˜ 100 and 160 ka. The noble gas mass spectrometric (U-Th)/He zircon age, corrected for disequilibrium and pre-eruptive storage, is 36 ± 3 ka. This result for the eruption age of La Vírgen tephra is significantly older than previously postulated historic or Holocene ages that were based on an 18th century map reference and 14C dating of accidental charcoal, respectively. The new (U-Th)/He zircon age is consistent with a > 26 ± 4 ka age derived from cosmogenic He exposure dating of an overlying basaltic lava flow [Hausback, B.P. and Abrams, M.J., 1996. Plinian eruption of La Virgen Tephra, Volcán Las Tres Virgenes, Baja California Sur, Mexico. Eos, Transactions, American Geophysical Union, 77(46, Suppl.): 813-814.]. U-Pb zircon analysis of ignimbrites erupted from the adjacent Early Pleistocene La Reforma and El Aguajito calderas yielded ages of 1.38 ± 0.03 Ma ( n = 12; MSWD = 1.0) and 1.17 ± 0.07 Ma ( n = 23; MSWD = 1.3), respectively. No evidence for these ages is found among La Vírgen zircons, whereas pre-Quaternary zircon xenocrysts are common. The La Vírgen magma, therefore, evolved unrelated to Early Pleistocene magmatism in adjacent calderas, but assimilated local basement rocks. A gap between average Th-U and (U-Th)/He zircon ages suggests that zircon crystallization was discontinuous in the La Vírgen magma chamber. In addition, partial resorption of zircon suggests episodic thermal rejuvenation, most likely by basaltic recharge. Based on the zircon record, the > 100 ka lifetime of the thermal anomaly that sustained repeated intrusive pulses significantly exceeds the age of the last eruption. This strengthens the view that Tres

  16. Sorption of 226Ra from waste effluents using Syrian bentonite.

    PubMed

    Al Attar, L; Al Masri, M S; Budeir, Y; Al Chayah, O

    2010-12-14

    In view of environmental concern, sorption of radium on natural bentonite mineral (Aleppo, Syria) was investigated using a batch-type method. Data were expressed in terms of distribution coefficients. An attempt to increase the selectivity of bentonite for radium was made by preparing M-derivatives. Loss of mineral crystallinity in acidic media and the formation of a new phase, such as BaCO3, in Ba-derivative were evidenced by XRD characterizations. Of the cationic forms, Na-bentonite showed the highest affinity. Mechanisms of radium uptake were studied using M-derivatives and simulated radium solutions. The obtained results indicated that surface sorption/surface ion exchange were the predominant processes. The distinct sorption behaviour observed with the Ba-form was, possibly, a reflection of radium coprecipitation with barium carbonate. The competing order of macro components, likely present in waste streams, was investigated by studying different concentrations of the corresponding salt media. Sodium was found to be the weakest inhibitor. The performance of natural bentonite and the most selective forms, i.e. Ba- and Na-derivatives, to sorb radium from actual oil co-produced waters, collected form Der Ezzor Petroleum Company (DEZPC), was studied. This showed the influential effect ofpH compared with other parameters.

  17. Rapid determination of 226Ra in environmental samples

    SciTech Connect

    Maxwell, Sherrod L.; Culligan, Brian K.

    2012-02-04

    A new rapid method for the determination of {sup 228}Ra in natural water samples has been developed at the SRNL/EBL (Savannah River National Lab/ Environmental Bioassay Laboratory) that can be used for emergency response or routine samples. While gamma spectrometry can be employed with sufficient detection limits to determine {sup 228}Ra in solid samples (via {sup 228}Ac) , radiochemical methods that employ gas flow proportional counting techniques typically provide lower MDA (Minimal Detectable Activity) levels for the determination of {sup 228}Ra in water samples. Most radiochemical methods for {sup 228}Ra collect and purify {sup 228}Ra and allow for {sup 228}Ac daughter ingrowth for ~36 hours. In this new SRNL/EBL approach, {sup 228}Ac is collected and purified from the water sample without waiting to eliminate this delay. The sample preparation requires only about 4 hours so that {sup 228}Ra assay results on water samples can be achieved in < 6 hours. The method uses a rapid calcium carbonate precipitation enhanced with a small amount of phosphate added to enhance chemical yields (typically >90%), followed by rapid cation exchange removal of calcium. Lead, bismuth, uranium, thorium and protactinium isotopes are also removed by the cation exchange separation. {sup 228}Ac is eluted from the cation resin directly onto a DGA Resin cartridge attached to the bottom of the cation column to purify {sup 228}Ac. DGA Resin also removes lead and bismuth isotopes, along with Sr isotopes and {sup 90}Y. La is used to determine {sup 228}Ac chemical yield via ICP-MS, but {sup 133}Ba can also be used instead if ICP-MS assay is not available. Unlike some older methods, no lead or strontium holdback carriers or continual readjustment of sample pH is required.

  18. Radioactivity in the groundwater of a high background radiation area.

    PubMed

    Shabana, E I; Kinsara, A A

    2014-11-01

    Natural radioactivity was measured in groundwater samples collected from 37 wells scattered in an inhabited area of high natural background radiation, in a purpose of radiation protection. The study area is adjacent to Aja heights of granitic composition in Hail province, Saudi Arabia. Initial screening for gross α and gross β activities showed levels exceeded the national regulation limits set out for gross α and gross β activities in drinking water. The gross α activity ranged from 0.17 to 5.41 Bq L(-)(1) with an average value of 2.15 Bq L(-)(1), whereas gross β activity ranged from 0.48 to 5.16 Bq L(-)(1), with an average value of 2.60 Bq L(-)(1). The detail analyses indicated that the groundwater of this province is contaminated with uranium and radium ((226)Ra and (228)Ra). The average activity concentrations of (238)U, (234)U, (226)Ra and (228)Ra were 0.40, 0.77, 0.29 and 0.46 Bq L(-)(1), respectively. The higher uranium content was found in the samples of granitic aquifers, whereas the higher radium content was found in the samples of sandstone aquifers. Based on the obtained results, mechanism of leaching of the predominant radionuclides has been discussed in detail.

  19. Neutron capture cross section measurement of 238U at the CERN n_TOF facility in the energy region from 1 eV to 700 keV

    NASA Astrophysics Data System (ADS)

    Mingrone, F.; Massimi, C.; Vannini, G.; Colonna, N.; Gunsing, F.; Žugec, P.; Altstadt, S.; Andrzejewski, J.; Audouin, L.; Barbagallo, M.; Bécares, V.; Bečvář, F.; Belloni, F.; Berthoumieux, E.; Billowes, J.; Bosnar, D.; Brugger, M.; Calviani, M.; Calviño, F.; Cano-Ott, D.; Carrapiço, C.; Cerutti, F.; Chiaveri, E.; Chin, M.; Cortés, G.; Cortés-Giraldo, M. A.; Diakaki, M.; Domingo-Pardo, C.; Duran, I.; Dressler, R.; Eleftheriadis, C.; Ferrari, A.; Fraval, K.; Ganesan, S.; García, A. R.; Giubrone, G.; Gonçalves, I. F.; González-Romero, E.; Griesmayer, E.; Guerrero, C.; Hernández-Prieto, A.; Jenkins, D. G.; Jericha, E.; Kadi, Y.; Käppeler, F.; Karadimos, D.; Kivel, N.; Koehler, P.; Kokkoris, M.; Krtička, M.; Kroll, J.; Lampoudis, C.; Langer, C.; Leal-Cidoncha, E.; Lederer, C.; Leeb, H.; Leong, L. S.; Lo Meo, S.; Losito, R.; Mallick, A.; Manousos, A.; Marganiec, J.; Martínez, T.; Mastinu, P. F.; Mastromarco, M.; Mendoza, E.; Mengoni, A.; Milazzo, P. M.; Mirea, M.; Mondalaers, W.; Paradela, C.; Pavlik, A.; Perkowski, J.; Plompen, A.; Praena, J.; Quesada, J. M.; Rauscher, T.; Reifarth, R.; Riego, A.; Robles, M. S.; Rubbia, C.; Sabaté-Gilarte, M.; Sarmento, R.; Saxena, A.; Schillebeeckx, P.; Schmidt, S.; Schumann, D.; Tagliente, G.; Tain, J. L.; Tarrío, D.; Tassan-Got, L.; Tsinganis, A.; Valenta, S.; Variale, V.; Vaz, P.; Ventura, A.; Vermeulen, M. J.; Vlachoudis, V.; Vlastou, R.; Wallner, A.; Ware, T.; Weigand, M.; Weiß, C.; Wright, T.; n TOF Collaboration

    2017-03-01

    The aim of this work is to provide a precise and accurate measurement of the 238U(n ,γ ) reaction cross section in the energy region from 1 eV to 700 keV. This reaction is of fundamental importance for the design calculations of nuclear reactors, governing the behavior of the reactor core. In particular, fast reactors, which are experiencing a growing interest for their ability to burn radioactive waste, operate in the high energy region of the neutron spectrum. In this energy region most recent evaluations disagree due to inconsistencies in the existing measurements of up to 15%. In addition, the assessment of nuclear data uncertainty performed for innovative reactor systems shows that the uncertainty in the radiative capture cross section of 238U should be further reduced to 1-3% in the energy region from 20 eV to 25 keV. To this purpose, addressed by the Nuclear Energy Agency as a priority nuclear data need, complementary experiments, one at the GELINA and two at the n_TOF facility, were proposed and carried out within the 7th Framework Project ANDES of the European Commission. The results of one of these 238U(n ,γ ) measurements performed at the n_TOF CERN facility are presented in this work. The γ -ray cascade following the radiative neutron capture has been detected exploiting a setup of two C6D6 liquid scintillators. Resonance parameters obtained from this work are on average in excellent agreement with the ones reported in evaluated libraries. In the unresolved resonance region, this work yields a cross section in agreement with evaluated libraries up to 80 keV, while for higher energies our results are significantly higher.

  20. Improved 206Pb/238U microprobe geochronology by the monitoring of a trace-element-related matrix effect; SHRIMP, ID-TIMS, ELA-ICP-MS and oxygen isotope documentation for a series of zircon standards

    USGS Publications Warehouse

    Black, L.P.; Kamo, S.L.; Allen, C.M.; Davis, D.W.; Aleinikoff, J.N.; Valley, J.W.; Mundil, R.; Campbell, I.H.; Korsch, R.J.; Williams, I.S.; Foudoulis, C.

    2004-01-01

    Precise isotope dilution-thermal ionisation mass spectrometry (ID-TIMS) documentation is given for two new Palaeozoic zircon standards (TEMORA 2 and R33). These data, in combination with results for previously documented standards (AS3, SL13, QGNG and TEMORA 1), provide the basis for a detailed investigation of inconsistencies in 206Pb/238U ages measured by microprobe. Although these ages are normally consistent between any two standards, their relative age offsets are often different from those established by ID-TIMS. This is true for both sensitive high-resolution ion-microprobe (SHRIMP) and excimer laser ablation-inductively coupled plasma-mass spectrometry (ELA-ICP-MS) dating, although the age offsets are in the opposite sense for the two techniques. Various factors have been investigated for possible correlations with age bias, in an attempt to resolve why the accuracy of the method is worse than the indicated precision. Crystallographic orientation, position on the grain-mount and oxygen isotopic composition are unrelated to the bias. There are, however, striking correlations between the 206Pb/238U age offsets and P, Sm and, most particularly, Nd abundances in the zircons. Although these are not believed to be the primary cause of this apparent matrix effect, they indicate that ionisation of 206Pb/238U is influenced, at least in part, by a combination of trace elements. Nd is sufficiently representative of the controlling trace elements that it provides a quantitative means of correcting for the microprobe age bias. This approach has the potential to reduce age biases associated with different techniques, different instrumentation and different standards within and between laboratories. Crown Copyright ?? 2004 Published by Elsevier B.V. All rights reserved.

  1. Measurement of the 238U neutron-capture cross section and gamma-emission spectra from 10 eV to 100 keV using the DANCE detector at LANSCE

    SciTech Connect

    Ullmann, John L; Couture, A J; Keksis, A L; Vieira, D J; O' Donnell, J M; Jandel, M; Haight, R C; Rundberg, R S; Kawano, T; Chyzh, A; Baramsai, B; Wu, C Y; Mitchell, G E; Becker, J A; Krticka, M

    2010-01-01

    A careful new measurement of the {sup 238}U(n,{gamma}) cross section from 10 eV to 100 keV has been made using the DANCE detector at LANSCE. DANCE is a 4{pi} calorimetric scintillator array consisting of 160 BaF{sub 2} crystals. Measurements were made on a 48 mg/cm{sup 2} depleted uranium target. The cross sections are in general good agreement with previous measurements. The gamma-ray emission spectra, as a function of gamma multiplicity, were also measured and compared to model calculations.

  2. Uranium and radium diffusion in organic-rich sediments (sapropels)

    NASA Astrophysics Data System (ADS)

    Gourgiotis, A.; Reyss, J.-L.; Frank, N.; Guihou, A.; Anagnostou, C.

    2011-09-01

    Among the late Quaternary Mediterranean sapropels, the S5 (125 ka) is one of the best preserved due to its high organic carbon content that has limited postdepositional oxidation. The high uranium content in this sapropel, >40 dpm g-1, makes this layer interesting for studying uranium series disequilibrium in organic-rich sediments. For this reason, the present work provides isotopic measurements of the U decay series in a S5 sapropel by applying more precise mass spectrometric methods, TIMS/MC-ICPMS, and gamma spectrometry. Assuming that U in the sapropel mostly originated from seawater the (234U/238U), (230Th/238U), (226Ra/230Th) and (231Pa/235U) activity ratios show systematic deviations from the theoretical values for a closed-system evolution of the U series over the 125 ka since sapropel formation. The radiogenic 234Urad and 226Ra show clear evidence of migration in the sapropel with modeled diffusion coefficients of (7.1 ± 1.1) × 10-12 cm2 s-1 and (1.6 ± 0.2) × 10-10 cm2 s-1, respectively. The diffusion of 234Urad cannot explain the high (230Th/238U) and (231Pa/235U) activity ratios observed in the sapropel. Two possible mechanisms or a combination of both are proposed for explaining the irregular (230Th/238U) and (231Pa/235U) activity profiles in sapropel S5. The first one is an enhanced export flux of 230Thxs and 231Paxs excesses exceeding the production rate in seawater, during the time of sapropel formation, and the second one is diffusion of authigenic Uauth in the sapropel. However, the ambiguous determination of 230Thxs and 231Paxs in the sapropel and the poorly understood processes that might lead to Uauth migration in anoxic sediments still limit a final explanation for the deviation of (230Th/238U) and (231Pa/235U) activity ratios from their expected theoretical values.

  3. Radionuclide concentrations in raw and purified phosphoric acids from Brazil and their processing wastes: implications for radiation exposures.

    PubMed

    da Conceição, Fabiano Tomazini; Antunes, Maria Lúcia Pereira; Durrant, Steven F

    2012-02-01

    Radionuclides from the U and Th natural series are present in alkaline rocks, which are used as feedstock in Brazil for the production of raw phosphoric acid, which can be considered as a NORM (naturally occurring radioactive material). As a result of the purification of raw phosphoric acid to food-grade phosphoric acid, two by-products are generated, i.e., solid and liquid wastes. Taking this into account, the main aim of this study was to evaluate the fluxes of natural radionuclide in the production of food-grade phosphoric acids in Brazil, to determine the radiological impact caused by ingestion of food-grade phosphoric acid, and to evaluate the solid waste environmental hazards caused by its application in crop soils. Radiological characterization of raw phosphoric acid, food-grade phosphoric acid, solid waste, and liquid waste was performed by alpha and gamma spectrometry. The (238)U, (234)U, (226)Ra, and (232)Th activity concentrations varied depending on the source of raw phosphoric acid. Decreasing radionuclides activity concentrations in raw phosphoric acids used by the producer of the purified phosphoric acid were observed as follows: Tapira (raw phosphoric acid D) > Catalão (raw phosphoric acids B and C) > Cajati (raw phosphoric acid A). The industrial purification process produces a reduction in radionuclide activity concentrations in food-grade phosphoric acid in relation to raw phosphoric acid produced in plant D and single raw phosphoric acid used in recent years. The most common use of food-grade phosphoric acid is in cola soft drinks, with an average consumption in Brazil of 72 l per person per year. Each liter of cola soft drink contains 0.5 ml of food-grade phosphoric acid, which gives an annual average intake of 36 ml of food-grade phosphoric acid per person. Under these conditions, radionuclide intake through consumption of food-grade phosphoric acid per year per person via cola soft drinks is not hazardous to human health in Brazil

  4. Time-dependent mean-field determination of the excitation energy in transfer reactions: Application to the reaction 238U on 12C at 6.14 MeV/nucleon

    NASA Astrophysics Data System (ADS)

    Scamps, G.; Rodríguez-Tajes, C.; Lacroix, D.; Farget, F.

    2017-02-01

    The internal excitation of nuclei after multinucleon transfer is estimated by using the time-dependent mean-field theory. Transfer probabilities for each channel as well as the energy loss after reseparation are calculated. By combining these two pieces of information, we show that the excitation energy distribution of the transfer fragments can be obtained separately for the different transfer channels. The method is applied to the reaction involving a 238U beam on a 12C target, which has recently been measured at GANIL. It is shown that the excitation energy calculated with the microscopic theory compares well with the experimental observation, provided that the competition with fusion is properly taken into account. The reliability of the excitation energy is further confirmed by the comparison with the phenomenological heavy-ion phase-space model at higher center-of-mass energies.

  5. Carbon export fluxes and export efficiency in the central Arctic during the record sea-ice minimum in 2012: a joint 234Th/238U and 210Po/210Pb study

    NASA Astrophysics Data System (ADS)

    Roca-Martí, Montserrat; Puigcorbé, Viena; Rutgers van der Loeff, Michiel M.; Katlein, Christian; Fernández-Méndez, Mar; Peeken, Ilka; Masqué, Pere

    2016-07-01

    The Arctic sea-ice extent reached a record minimum in September 2012. Sea-ice decline increases the absorption of solar energy in the Arctic Ocean, affecting primary production and the plankton community. How this will modulate the sinking of particulate organic carbon (POC) from the ocean surface remains a key question. We use the 234Th/238U and 210Po/210Pb radionuclide pairs to estimate the magnitude of the POC export fluxes in the upper ocean of the central Arctic in summer 2012, covering time scales from weeks to months. The 234Th/238U proxy reveals that POC fluxes at the base of the euphotic zone were very low (2 ± 2 mmol C m-2 d-1) in late summer. Relationships obtained between the 234Th export fluxes and the phytoplankton community suggest that prasinophytes contributed significantly to the downward fluxes, likely via incorporation into sea-ice algal aggregates and zooplankton-derived material. The magnitude of the depletion of 210Po in the upper water column over the entire study area indicates that particle export fluxes were higher before July/August than later in the season. 210Po fluxes and 210Po-derived POC fluxes correlated positively with sea-ice concentration, showing that particle sinking was greater under heavy sea-ice conditions than under partially ice-covered regions. Although the POC fluxes were low, a large fraction of primary production (>30%) was exported at the base of the euphotic zone in most of the study area during summer 2012, indicating a high export efficiency of the biological pump in the central Arctic.

  6. The mechanisms and timescales of rhyolite generation at Yellowstone caldera: New insights from 238U-230Th crystallization ages, trace-elements, and isotope compositions of zircon and sanidine

    NASA Astrophysics Data System (ADS)

    Stelten, M. E.; Cooper, K. M.; Vazquez, J. A.; Calvert, A. T.

    2013-12-01

    The Yellowstone Plateau hosts one of the largest Quaternary magmatic systems on Earth, with caldera forming eruptions at ~2.1 Ma, ~1.3 Ma, and ~0.64 Ma, as well as numerous intracaldera rhyolitic eruptions between caldera-forming events. The most recent post-caldera eruptive episode at Yellowstone produced the Central Plateau Member (CPM) of the Plateau Rhyolite, which erupted intermittently between ca. 170-70 ka with a cumulative volume ≥600 km3. Thus, the CPM rhyolites provide snapshots of a large silicic magmatic system though time. We examine five CPM rhyolites that erupted from ~125 ka to ~70 ka, and constrain the mechanisms and timescales of generating eruptible rhyolites at Yellowstone caldera by comparing (1) 238U-230Th crystallization ages and trace-element compositions of the interiors and surfaces (i.e., unpolished rims) of individual zircons with (2) bulk 238U-230Th crystallization ages and in situ major-element, Ba, and Pb isotope data for sanidines hosted in each rhyolite. The zircon age and trace-element data show that zircons in CPM rhyolites record crystallization from their respective eruption age to >150 ka before eruption, with most zircon surfaces crystallizing close to eruption and many interiors crystallizing 10 kyr to 150 kyr before eruption. At any given age, zircon surfaces have homogeneous trace-element compositions relative to zircon interiors for most elements and element ratios. For example, when considering data from all five CPM rhyolites, the zircon surfaces and interiors show similar broad trends in Eu/Eu* and U/Th over time, but the surfaces display less scatter. These observations suggest that the zircon surfaces grew from a more homogeneous region of the magma reservoir relative to where the zircon interiors grew. Although the zircon surfaces and interiors are similar in some elements and element ratios (e.g., Eu/Eu*, U/Th) at a given age, zircon surfaces and interiors display distinct (Y, MREE, HREE)/(P, U) ratios at a given

  7. Characterization of contaminant transport using naturally-occurring U-series disequilibria. 1998 annual progress report

    SciTech Connect

    Murrell, M.; Ku, T.L.

    1998-06-01

    'The goal of the research is to study the migratory behavior of contaminants in subsurface fractured systems using naturally occurring uranium- and thorium-series radionuclides as tracers under in-situ physico-chemical and hydrogeologic conditions. Naturally occurring U- and Th-series disequilibria can provide information on the rates of adsorption-desorption and transport of contaminants as well as on fluid transport and rock dissolution in a natural setting. The authors are developing a realistic model of contaminant migration in the Snake River Plain Aquifer beneath the INEEL by evaluating the retardation processes involved in the rock/water interaction. The major tasks are to: (1) determine the natural distribution of U, Th, Pa and Ra isotopes in the groundwater as well as in rock minerals and sorbed phases, and (2) study rock/water interaction processes using U/Th series disequilibria and a statistical analysis-based model code for the calculation of in-situ retardation factors of radionuclides and rock/water interaction time scales. This study will also provide an improved understanding of the hydrogeologic features of the site and their impact on the migration of contaminants. This report summarizes results after 20 months of a 36-month project. Studies performed at LANL include analysis of the long-lived nuclides {sup 238}U, {sup 235}U, {sup 234}U, {sup 230}Th, {sup 226}Ra, {sup 232}Th, and {sup 231}Pa by thermal ionization mass spectrometry (TIMS). Studies performed at the Univ. of Southern California include the measurement of short-lived naturally occurring radionuclides by decay-counting techniques and the development of models to predict the migration behavior of these radionuclides. Initial efforts began with analysis of 31, 0.5L water samples obtained through routine sampling by USGS and INEEL personnel. One significant observation from these data is that {sup 234}U/{sup 238}U activity ratios are highest in waters that emanate from local recharge

  8. Neutron Resonance Parameters of 238U and the Calculated Cross Sections from the Reich-Moore Analysis of Experimental Data in the Neutron Energy Range from 0 keV to 20 keV

    SciTech Connect

    Derrien, H

    2005-12-05

    The neutron resonance parameters of {sup 238}U were obtained from a SAMMY analysis of high-resolution neutron transmission measurements and high-resolution capture cross section measurements performed at the Oak Ridge Electron Linear Accelerator (ORELA) in the years 1970-1990, and from more recent transmission and capture cross section measurements performed at the Geel Linear Accelerator (GELINA). Compared with previous evaluations, the energy range for this resonance analysis was extended from 10 to 20 keV, taking advantage of the high resolution of the most recent ORELA transmission measurements. The experimental database and the method of analysis are described in this report. The neutron transmissions and the capture cross sections calculated with the resonance parameters are compared with the experimental data. A description is given of the statistical properties of the resonance parameters and of the recommended values of the average parameters. The new evaluation results in a slight decrease of the effective capture resonance integral and improves the prediction of integral thermal benchmarks by 70 pcm to 200 pcm.

  9. Neutron spectral and angular distribution measurements for 113 and 256 MeV protons on range-thick Al and sup 238 U targets using the foil activation techniques

    SciTech Connect

    Greenwood, L.R.; Intasorn, A.

    1989-07-01

    Second neutron yields, energy spectra, and angular distributions have been measured at seven angles from 0 to 150{degree} for 113 and 256 MeV protons stopped in range-thick targets of aluminum and depleted uranium ({sup 238}U). Thin foil stacks of ten different materials were activated by secondary neutrons at distances of 20--30 cm from the targets. Following each irradiation, 30--40 different activation products were measured by gamma-ray spectroscopy. These activation rates were then used to adjust neutron energy spectra calculated by the HETC computer code. Activation cross sections were taken from ENDF/BV below 20 MeV, from literature values tested in Be(d,n) fields up to 50 MeV, and from proton spallation data and calculations from 50--250 MeV. Spectral adjustments were made with the STAY'SL computer code using a least-squares technique to minimize {chi}{sup 2} for a covariance matrix determined from uncertainties in the measured activities, cross sections, and calculated flux spectra. Neutron scattering effects were estimated from foil packets irradiated at different distances from the target. Proton effects were measured with (p,n) reactions. Systematic differences were found between the adjusted and calculated neutron spectra, namely, that HETC underpredicts the neutron flux at back angles by a factor of 2--3 and slightly overpredicts the flux at forward angles. 19 refs., 23 figs., 13 tabs.

  10. Neutron scattering cross sections for /sup 232/Th and /sup 238/U inferred from proton scattering and charge exchange measurements. [7 MeV, 26 and 27 MeV

    SciTech Connect

    Hansen, L.F.; Grimes, S.M.; Pohl, B.A.; Poppe, C.H.; Wong, C.

    1980-01-01

    Differential cross sections for the (p,n) reactions to the isobaric analog states (IAS) of /sup 232/Th and /sup 238/U targets were measured at 26 and 27 MeV. The analysis of the data was done in conjunction with the proton elastic and inelastic (2/sup +/, 4/sup +/, 6/sup +/) differential cross sections measured at 26 MeV. Because collective effects are important in this mass region, deformed coupled-channels calculations were carried out for the simultaneous analysis of the proton and neutron outgoing channels. The sensitivity of the calculations was studied with respect to the optical model parameters used in the calculations, the shape of the nuclear charge distribution, the type of coupling scheme assumed among the levels, the magnitude of the deformation parameters, and the magnitude of the isovector potentials, V/sub 1/ and W/sub 1/. A Lane model-consistent analysis of the data was used to infer optical potential parameters for 6- to 7-MeV neutrons. The neutron elastic differential cross sections obtained from these calculations are compared with measurements available in the literature, and with results obtained using neutron parameters from global sets reported at these energies. 7 figures, 3 tables.

  11. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, M.; Arnold, C.; Bredeweg, T.; Vieira, D.; Wilhelmy, J.; Tonchev, A.; Stoyer, M.; Bhike, M.; Krishichayan, F.; Tornow, W.; Fowler, M.

    2015-10-01

    Under a joint collaboration between TUNL-LANL-LLNL, a set of absolute fission product yield measurements has been performed. The energy dependence of a number of cumulative fission product yields (FPY) have been measured using quasi-monoenergetic neutron beams for three actinide targets, 235U, 238U and 239Pu, between 0.5 and 14.8 MeV. The FPYs were measured by a combination of fission counting using specially designed dual-fission chambers and ?-ray counting. Each dual-fission chamber is a back-to-back ionization chamber encasing an activation target in the center with thin deposits of the same target isotope in each chamber. This method allows for the direct measurement of the total number of fissions in the activation target with no reference to the fission cross-section, thus reducing uncertainties. ?-ray counting of the activation target was performed on well-shielded HPGe detectors over a period of 2 months post irradiation to properly identify fission products. Reported are absolute cumulative fission product yields for incident neutron energies of 0.5, 1.37, 2.4, 3.6, 4.6, 5.5, 7.5, 8.9 and 14.8 MeV. These results are compared to previous measurements and theoretical estimates. This work was performed under the auspices of the USDoE by Los Alamos National Security, LLC under Contract DE-AC52-06NA25396.

  12. POC and particulate 234 Th export fluxes estimated using 234 Th/ 238 U disequilibrium in an enclosed Eastern Mediterranean region (Saronikos Gulf and Elefsis Bay, Greece) in seasonal scale

    NASA Astrophysics Data System (ADS)

    Evangeliou, Nikolaos; Florou, Heleny; Scoullos, Michael

    2011-10-01

    Activity concentrations of the naturally occurring, short-lived and highly particle-reactive radionuclide tracer 234Th in the dissolved and particulate phase were determined at 7 shallow-water stations (maximum depths: 30 (S.1 and S.2), 65 (S.3), 97 (S.5), 105 (S.6) and 220 m (S.4 and S.7) in Saronikos Gulf and Elefsis Bay (central Aegean Sea, Greece) during 3 seasonal cruises (summer 2008, autumn 2008 and winter 2009) to assess the time scales of the dynamics and the depositional fate of particulate matter (POC, particulate 234Th). For that reason, in situ filtrating systems were deployed in several depths of the water column consisting of GF/A disc prefilters to scavenge particulate fraction of 234Th and organic carbon and impregnated cartridges to adsorb dissolved 234Th. The obtained data showed average particulate 234Th activity concentrations of 3.7 ± 0.4 Bq m -3 in summer, 2.1 ± 0.2 Bq m -3 in autumn and 2.4 ± 0.2 Bq m -3 in winter. The respective average dissolved 234Th activity concentrations were 30.1 ± 2.8 Bq m -3 in summer, 30.2 ± 2.9 Bq m -3 in autumn and 27.4 ± 3.0 Bq m -3 in winter. The activity ratios of total 234Th and its long-lived conservative parent 238U were below unity in most of the stations indicating radioactive disequilibrium throughout the water column, thus very dynamic trace-metal scavenging and particle export from the water column. These profiles ( 234Th and 238U) were used to estimate the export fluxes and scavenging rates of 234Th, as well as their residence times in the water column. The average cumulative export fluxes of particulate 234Th were estimated to be 33 ± 4 Bq m -2 d -1 in summer, 35 ± 5 Bq m -2 d -1 in autumn and 45 ± 6 Bq m -2 d -1 in winter, whereas the respective average cumulative scavenging rates of dissolved 234Th were 39 ± 5, 33 ± 5 and 50 ± 7 Bq m -2 d -1. Moreover, the cumulative average residence times of 234Th were 25 ± 4 d in summer, 45 ± 6 d in autumn and 64 ± 7 d in winter 2009 for the

  13. Cogenetic late Pleistocene rhyolite and cumulate diorites from Augustine Volcano revealed by SIMS 238U-230Th dating of zircon, and implications for silicic magma generation by extraction from mush

    NASA Astrophysics Data System (ADS)

    Coombs, Michelle L.; Vazquez, Jorge A.

    2014-12-01

    Volcano, a frequently active andesitic island stratocone, erupted a late Pleistocene rhyolite pumice fall that is temporally linked through zircon geochronology to cumulate dioritic blocks brought to the surface in Augustine's 2006 eruption. Zircon from the rhyolite yield a 238U-230Th age of ˜25 ka for their unpolished rims, and their interiors yield a bimodal age populations at ˜26 ka and a minority at ˜41 ka. Zircon from dioritic blocks, ripped from Augustine's shallow magmatic plumbing system and ejected during the 2006 eruption, have interiors defining a ˜26 ka age population that is indistinguishable from that for the rhyolite; unpolished rims on the dioritic zircon are dominantly younger (≤12 ka) indicating subsequent crystallization. Zircon from rhyolite and diorite overlap in U, Hf, Ti, and REE concentrations although diorites also contain a second population of high-U, high temperature grains. Andesites that brought dioritic blocks to the surface in 2006 contain zircon with young (≤9 ka) rims and a scattering of older ages, but few zircon that crystallized during the 26 ka interval. Both the Pleistocene-age rhyolite and the 2006 dioritic inclusions plot along a whole-rock compositional trend distinct from mid-Holocene-present andesites and dacites, and the diorites, rhyolite, and two early Holocene dacites define linear unmixing trends often oblique to the main andesite array and consistent with melt (rhyolite) extraction from a mush (dacites), leaving behind a cumulate amphibole-bearing residue (diorites). Rare zircon antecrysts up to ˜300 ka from all rock types indicate that a Quaternary center has been present longer than preserved surficial deposits.

  14. Magma mixing and the generation of isotopically juvenile silicic magma at Yellowstone caldera inferred from coupling 238U-230Th ages with trace elements and Hf and O isotopes in zircon and Pb isotopes in sanidine

    NASA Astrophysics Data System (ADS)

    Stelten, Mark E.; Cooper, Kari M.; Vazquez, Jorge A.; Reid, Mary R.; Barfod, Gry H.; Wimpenny, Josh; Yin, Qing-zhu

    2013-08-01

    The nature of compositional heterogeneity within large silicic magma bodies has important implications for how silicic reservoirs are assembled and evolve through time. We examine compositional heterogeneity in the youngest (~170 to 70 ka) post-caldera volcanism at Yellowstone caldera, the Central Plateau Member (CPM) rhyolites, as a case study. We compare 238U-230Th age, trace-element, and Hf isotopic data from zircons, and major-element, Ba, and Pb isotopic data from sanidines hosted in two CPM rhyolites (Hayden Valley and Solfatara Plateau flows) and one extracaldera rhyolite (Gibbon River flow), all of which erupted near the caldera margin ca. 100 ka. The Hayden Valley flow hosts two zircon populations and one sanidine population that are consistent with residence in the CPM reservoir. The Gibbon River flow hosts one zircon population that is compositionally distinct from Hayden Valley flow zircons. The Solfatara Plateau flow contains multiple sanidine populations and all three zircon populations found in the Hayden Valley and Gibbon River flows, demonstrating that the Solfatara Plateau flow formed by mixing extracaldera magma with the margin of the CPM reservoir. This process highlights the dynamic nature of magmatic interactions at the margins of large silicic reservoirs. More generally, Hf isotopic data from the CPM zircons provide the first direct evidence for isotopically juvenile magmas contributing mass to the youngest post-caldera magmatic system and demonstrate that the sources contributing magma to the CPM reservoir were heterogeneous in 176Hf/177Hf at ca. 100 ka. Thus, the limited compositional variability of CPM glasses reflects homogenization occurring within the CPM reservoir, not a homogeneous source.

  15. Beta and gamma decay heat measurements between 0.1s - 50,000s for neturon fission of {sup 235}U, {sup 238}U and {sup 239}Pu. Progress report, June 1, 1992--December 31, 1994

    SciTech Connect

    Schier, W.A.; Couchell, G.P.

    1997-05-01

    In the investigations reported here, a helium-jet/tape-transport system was used for the rapid transfer of fission products to a low-background environment where their aggregate beta and gamma-ray spectra were measured as a function of delay time after neutron induced fission of {sup 235}U, {sup 238}U and {sup 239}Pu. Beta and gamma-ray energy distributions have been deduced for delay times as short as 0.2 s and extending out to 100,000s. Instrumentation development during the initial phase of the project included: (1) assembly and characterization of a NaI(Tl) spectrometer for determining aggregate gamma-ray energy distributions, (2) development and characterization of a beta spectrometer (having excellent gamma-ray rejection) for measuring aggregate beta-particle energy distributions, (3) assembly and characterization of a Compton-suppressed HPGe spectrometer for determining gamma-ray intensities of individual fission products to deduce fission-product yields. Spectral decomposition and analysis codes were developed for deducing energy distributions from measured aggregate beta and gamma spectra. The aggregate measurements in the time interval 0.2 - 20s after fission are of special importance since in this region data from many short-lived nuclei are missing and summation calculations in this region rely on model calculations for a large fraction of their predicted beta and gamma decay heat energy spectra. Comparison with ENDF/B-VI fission product data was performed in parallel with the measurements through a close collaboration with Dr. T. England at LANL, assisted by one of our graduate students. Such aggregate measurements provide tests of the Gross Theory of beta decay used to calculated missing contributions to this data base. Fission-product yields deduced from the HPGe studies will check the accuracy of the semi-empirical Gaussian dispersion model used presently by evaluators in the absence of measured yields.

  16. Uranium series disequilibrium in a young surficial uranium deposit, northeastern Washington, U.S.A.

    USGS Publications Warehouse

    Zielinski, R.A.; Bush, C.A.; Rosholt, J.N.

    1986-01-01

    A recently discovered ore-grade accumulation of U in organic-rich sediments of late Quaternary age provides an opportunity for studying the early association of U, U-daughters, and organic matter in a natural setting. The U occurs in valley-fill sediments of peat, peaty clay, silt, and sand along the north fork of Flodelle Creek, Stevens County, Washington. Radiometric techniques (delayed neutron, high-resolution gamma-ray spectrometry, thin-source alpha spectrometry) were employed to determine the abundance and distribution of U-series nuclides, the extent of secular equilibrium within the U decay series, and the apparent U-series ages of U incorporation. Sixteen lithologically distinct intervals were sampled from a 292 cm core. Uranium contents range from 140 to 2790 ppm and are positively correlated with organic contents. Measured alpha activity ratios of 234U/238U (1.31-1.38) are very similar to those reported in coexisting waters, suggesting a rather constant isotopic composition of introduced U. Much lower Th contents of <10-40 ppm are controlled by the type and abundance of silicate detritus. The youth of the host sediments (<15 000 a) and the paucity of associated radioactivity suggested large excesses of U relative to radioactive daughters and such excesses were observed, particularly in the shallowest intervals. Apparent ages of U emplacement determined by the (alpha) activity ratio of 230Th daughter to 234U parent show a general increase with depth and fair agreement with estimated depositional ages. This observation suggests dominantly syndepositional or early post depositional emplacement of U followed by decay-generated buildup of 230Th daughter with time. However, interval by interval comparisons of the relative abundances of other daughters, particularly 226Ra and 210Pb, indicate variability caused by processes other than closed-system growth and decay, probably because chemically diverse daughters that are decay-generated in situ have differing

  17. Constrains on the Uranium Isotopic Composition of Seawater and Implications for Coral U/Th Geochronology

    NASA Astrophysics Data System (ADS)

    Chutcharavan, P. M.; Dutton, A.; Ellwood, M. J.

    2015-12-01

    Coral U-series geochronology is an important tool for calibrating records of sea level change during the late Quaternary and coral 14C dates for the radiocarbon timescale. However, coralline aragonite is highly susceptible to diagenesis, and samples must be carefully screened to ensure a specimen is unaltered. One method used to accept or reject U-series ages is the initial coral 234U/238U activity ratio, which reflects the 234U/238U activity of seawater at the time of coral skeleton formation. Due to the long residence time of uranium in the ocean (~400,000 years), researchers often assume that seawater 234U/238U has remained constant throughout the late Pleistocene. Coral specimens whose U-series ages yield an initial 234U/238U value that is significantly different than modern seawater are considered altered. Several studies have demonstrated that coral initial 234U/238U and, hence, seawater 234U/238U may have varied significantly on glacial-interglacial timescales, but the cause of this variability is subject to debate. To evaluate the pattern and mechanisms of 234U/238U variability in seawater over the last glacial cycle, we draw upon a compilation of U-series measurements of shallow and deep water corals to better define the observed variability. Observed trends from the coral record will be assessed using a simple two-box model of the ocean to determine how changes to the ocean's uranium isotope budget during glacial cycles can explain shifts in seawater 234U/238U. An improved understanding the evolution of seawater 234U/238U composition will enable more robust interpretations of both closed-system and open-system ages for corals. Such interpretations of U-series ages are essential to the development of robust chronologies for climate and sea level change and for improving the calibration of the radiocarbon timescale.

  18. Distribution of natural radionuclides in the production and use of phosphate fertilizers in Brazil.

    PubMed

    Saueia, C H R; Mazzilli, B P

    2006-01-01

    The Brazilian phosphate fertilizer is obtained by wet reaction of igneous phosphate rock with concentrated sulphuric acid, giving as final product, phosphoric acid and dehydrated calcium sulphate (phosphogypsum) as by-products. Phosphoric acid is the starting material for triple superphosphate (TSP), single superphosphate (SSP), monoammonium phosphate (MAP) and diammonium phosphate (DAP). The phosphate rock used as raw material presents in its composition radionuclides of the U and Th natural series. Taking this into account, the main aim of this paper is to evaluate the fluxes of natural radionuclides and radioactive disequilibria involved in the Brazilian industrial process of phosphoric acid production; to determine the content of radioactivity in several commercial fertilizers produced by this industry; to estimate their radiological impact in crop soils and the long term exposure due to their application. Radiological characterization of phosphate rock, phosphogypsum and phosphate fertilizers was performed by alpha and gamma spectrometry. The fertilizer samples, which are derived directly from phosphoric acid, MAP and DAP, presented in their composition low activity concentrations for 226Ra, 228Ra and 210Pb. As for U and Th, the concentrations found in MAP and DAP are more significant, up to 822 and 850Bqkg(-1), respectively. SSP and TSP, which are obtained by mixing phosphoric acid with different amounts of phosphate rock, presented higher concentrations of radionuclides, up to 1158Bqkg(-1) for (238)U, 1167Bqkg(-1) for (234)U, 1169Bqkg(-1) for 230Th, 879Bqkg(-1) for 226Ra, 1255Bqkg(-1) for 210Pb, 521Bqkg(-1) for 232Th, 246Bqkg(-1) for 228Ra and 302Bqkg(-1) for 228Th. Long term exposure due to successive fertilizer applications was evaluated. Internal doses due to the application of phosphate fertilizer for 10, 50 and 100 years were below 1mSvy(-1), showing that the radiological impact of such practice is negligible.

  19. Radon loss from barite in submarine hydrothermal sulfide deposits

    NASA Astrophysics Data System (ADS)

    Uchida, A.; Toyoda, S.; Ishibashi, J.

    2012-12-01

    Determining the ages of the hydrothermal deposit will greatly contribute the studies of temporal change of submarine hydrothermal activities, as they are essential factors for ore formation and for the biological systems sustained by the chemical species arising from hydrothermal activities. The dating methods available for this purpose includes disequilibrium among 238U, 234U, and 230Th in sufide minerals, between 226Ra and 210Pb, and 228Ra and 228Th in barite (BaSO4) contained in the deposits, and ESR (electron spin resonance) using SO3- radical in barite. In applying these dating methods, a closed system is assumed, where radioactive nuclei decay following the law of physics but are not mobile out of the mineral. However, White and Rood (2001) reported that 3 to 20% of 222Rn is lost from barite crystal, which are used for casing of mining on the land. As 222Rn loss in barite greatly affects the dating results of 226}Ra-{210Pb method and ESR dating method in which radioactive equilibrium is assumed to calculate the dose rate, in the present paper, we investigated {222}Rn loss from the barite crystals contained in hydrothermal sulfide deposits. The radioactive nuclei, 210Pb and 214Bi were measured by the low background pure germanium gamma ray spectrometer at Okayama University of Science. A Pitchblend Uraninite (UO2) mixed with NaCl was used as the equilibrated standard. The barite crystals extracted from hydrothermal sulfide deposits taken in South Mariana Trough are also crused and mixed with NaCl. The mixed powder was packed in a thin stainless container which prevent from Rn loss, before the measurements. The measurements for 24 hours were repeated every day for 20 days. As results, it was found that the peak intensities of 210Pb and 214Bi did not change with time, meaning no Rn loss.

  20. Energy Dependence of Fission Product Yields from {sup 235}U, {sup 238}U and {sup 239}Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    SciTech Connect

    Gooden, M.E.; Arnold, C.W.; Becker, J.A.; Bhatia, C.; Bhike, M.; Bond, E.M.; Bredeweg, T.A.; Fallin, B.; Fowler, M.M.; Howell, C.R.; Kelley, J.H.; Krishichayan; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S.A.; Stoyer, M.A.; Tonchev, A.P.; Tornow, W.; and others

    2016-01-15

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for {sup 235}U, {sup 238}U and {sup 239}Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission chamber

  1. Energy Dependence of Fission Product Yields from 235U, 238U and 239Pu for Incident Neutron Energies Between 0.5 and 14.8 MeV

    NASA Astrophysics Data System (ADS)

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; Bhatia, C.; Bhike, M.; Bond, E. M.; Bredeweg, T. A.; Fallin, B.; Fowler, M. M.; Howell, C. R.; Kelley, J. H.; Krishichayan; Macri, R.; Rusev, G.; Ryan, C.; Sheets, S. A.; Stoyer, M. A.; Tonchev, A. P.; Tornow, W.; Vieira, D. J.; Wilhelmy, J. B.

    2016-01-01

    Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varying degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual-fission chamber and gamma

  2. Energy dependence of fission product yields from 235U, 238U and 239Pu for incident neutron energies between 0.5 and 14.8 MeV

    DOE PAGES

    Gooden, M. E.; Arnold, C. W.; Becker, J. A.; ...

    2016-01-06

    In this study, Fission Product Yields (FPY) have historically been one of the most observable features of the fission process. They are known to have strong variations that are dependent on the fissioning species, the excitation energy, and the angular momentum of the compound system. However, consistent and systematic studies of the variation of these FPY with energy have proved challenging. This is caused primarily by the nature of the experiments that have traditionally relied on radiochemical procedures to isolate specific fission products. Although radiochemical procedures exist that can isolate all products, each element presents specific challenges and introduces varyingmore » degrees of systematic errors that can make inter-comparison of FPY uncertain. Although of high importance in fields such as nuclear forensics and Stockpile Stewardship, accurate information about the energy dependence of neutron induced FPY are sparse, due primarily to the lack of suitable monoenergetic neutron sources. There is a clear need for improved data, and to address this issue, a collaboration was formed between Los Alamos National Laboratory (LANL), Lawrence Livermore National Laboratory (LLNL) and the Triangle Universities Nuclear Laboratory (TUNL) to measure the energy dependence of FPY for 235U, 238U and 239Pu. The measurements have been performed at TUNL, using a 10 MV Tandem Van de Graaff accelerator to produce monoenergetic neutrons at energies between 0.6 MeV to 14.8 MeV through a variety of reactions. The measurements have utilized a dual-fission chamber, with thin (10-100 μg/cm2) reference foils of similar material to a thick (100-400 mg) activation target held in the center between the chambers. This method allows for the accurate determination of the number of fissions that occurred in the thick target without requiring knowledge of the fission cross section or neutron fluence on target. Following activation, the thick target was removed from the dual

  3. Radon (222Rn) in ground water of fractured rocks: a diffusion/ion exchange model.

    PubMed

    Wood, Warren W; Kraemer, Thomas F; Shapiro, Allen

    2004-01-01

    Ground waters from fractured igneous and high-grade sialic metamorphic rocks frequently have elevated activity of dissolved radon (222Rn). A chemically based model is proposed whereby radium (226Ra) from the decay of uranium (238U) diffuses through the primary porosity of the rock to the water-transmitting fracture where it is sorbed on weathering products. Sorption of 226Ra on the fracture surface maintains an activity gradient in the rock matrix, ensuring a continuous supply of 226Ra to fracture surfaces. As a result of the relatively long half-life of 226Ra (1601 years), significant activity can accumulate on fracture surfaces. The proximity of this sorbed 226Ra to the active ground water flow system allows its decay progeny 222Rn to enter directly into the water. Laboratory analyses of primary porosity and diffusion coefficients of the rock matrix, radon emanation, and ion exchange at fracture surfaces are consistent with the requirements of a diffusion/ion-exchange model. A dipole-brine injection/withdrawal experiment conducted between bedrock boreholes in the high-grade metamorphic and granite rocks at the Hubbard Brook Experimental Forest, Grafton County, New Hampshire, United States (42 degrees 56'N, 71 degrees 43'W) shows a large activity of 226Ra exchanged from fracture surfaces by a magnesium brine. The 226Ra activity removed by the exchange process is 34 times greater than that of 238U activity. These observations are consistent with the diffusion/ion-exchange model. Elutriate isotopic ratios of 223Ra/226Ra and 238U/226Ra are also consistent with the proposed chemically based diffusion/ion-exchange model.

  4. Radon (222Rn) in ground water of fractured rocks: A diffusion/ion exchange model

    USGS Publications Warehouse

    Wood, W.W.; Kraemer, T.F.; Shapiro, A.

    2004-01-01

    Ground waters from fractured igneous and high-grade sialic metamorphic rocks frequently have elevated activity of dissolved radon (222Rn). A chemically based model is proposed whereby radium (226Ra) from the decay of uranium (238U) diffuses through the primary porosity of the rock to the water-transmitting fracture where it is sorbed on weathering products. Sorption of 226Ra on the fracture surface maintains an activity gradient in the rock matrix, ensuring a continuous supply of 226Ra to fracture surfaces. As a result of the relatively long half-life of 226Ra (1601 years), significant activity can accumulate on fracture surfaces. The proximity of this sorbed 226Ra to the active ground water flow system allows its decay progeny 222Rn to enter directly into the water. Laboratory analyses of primary porosity and diffusion coefficients of the rock matrix, radon emanation, and ion exchange at fracture surfaces are consistent with the requirements of a diffusion/ion- exchange model. A dipole-brine injection/withdrawal experiment conducted between bedrock boreholes in the high-grade metamorphic and granite rocks at the Hubbard Brook Experimental Forest, Grafton County, New Hampshire, United States (42??56???N, 71??43???W) shows a large activity of 226Ra exchanged from fracture surfaces by a magnesium brine. The 226Ra activity removed by the exchange process is 34 times greater than that of 238U activity. These observations are consistent with the diffusion/ion-exchange model. Elutriate isotopic ratios of 223Ra/226Ra and 238U/226Ra are also consistent with the proposed chemically based diffusion/ion-exchange model.

  5. Radioactivity of cigarettes and the importance of (210)Po and thorium isotopes for radiation dose assessment due to smoking.

    PubMed

    Kubalek, Davor; Serša, Gregor; Štrok, Marko; Benedik, Ljudmila; Jeran, Zvonka

    2016-05-01

    Tobacco and tobacco smoke are very complex mixtures. In addition to various chemical and organic compounds they also contain natural radioactive elements (radionuclides). In this work, the natural radionuclide activity concentrations ((234)U, (238)U, (228)Th, (230)Th, (232)Th, (226)Ra, (210)Pb and (210)Po) of nine different cigarette samples available on the Slovenian market are reported. In addition to (210)Po, the transfer of thorium isotopes from a cigarette to a smoker's body and lungs have been determined for the first time. Cigarette smoke and exhaled air from smokers' lungs were collected from volunteer smokers (C-4 brand) to determinate what quantity of (210)Po and thorium isotopes is transferred from the tobacco to the smoker's lungs. Cigarette ash and smoked filters were also collected and analysed. Among the determined isotopes, (210)Pb and (210)Po showed the highest activity concentrations. During the smoking of one cigarette approximately 22% of (210)Po (and presumably its predecessor (210)Pb), 0.6% of (228)Th, 24% of (230)Th, and 31% of (232)Th are transferred from the cigarette and retained in the smoker's body. The estimated annual effective dose for smokers is 61 μSv/year from (210)Po; 9 μSv/year from (210)Pb; 6 μSv/year from (228)Th; 47 μSv/year from (230)Th, and 37 μSv/year from (232)Th. These results show the importance of thorium isotopes in contributing to the annual effective dose for smoking.

  6. Health Effects Due to Radionuclides Content of Solid Minerals within Port of Richards Bay, South Africa

    PubMed Central

    Masok, Felix B.; Masiteng, Paulus L.; Mavunda, Risimati D.; Maleka, Peane P.

    2016-01-01

    This study assessed the radiological health hazards to various body organs of workers working within Transnet Precinct in Richards Bay in Kwazulu-Natal, South Africa due to radionuclide content of mineral ores often stored within the facility. Thirty samples were collected from five mineral ores (rock phosphate, rutile, zircon, coal and hematite) and analyzed for 238U, 234U, 226Ra, 210Pb, 235U, 232Th, 228Ra, 228Th and 40K using delayed neutron activation analysis and low energy gamma spectroscopy. Rutile was found to be the most radioactive mineral ore within the facility with 210Pb concentration of 759.00 ± 106.00 Bq·kg−1. Effective annual dose rate in (mSv·y−1) delivered to different organs of the body: testes, bone marrow, whole body, lungs and ovaries from mineral ores were such that dose from mineral ores decreased in the order coal > rutile > rock phosphate > hematite > zircon. The organs with the highest received dose rate were the testes and this received dose was from coal. However, all of the calculated absorbed dose rates to organs of the body were below the maximum permissible safety limits. PMID:27898013

  7. AIR AND RADON PATHWAY MODELING FOR THE F AREA TANK FARM

    SciTech Connect

    Dixon, K.; Phifer, M.

    2010-07-30

    An air and radon pathways analysis was conducted for the F-Area Tank Farm (FTF) to estimate the flux of volatile radionuclides and radon at the ground surface due to residual waste remaining in the tanks following closure. This analysis was used as the basis to estimate the dose to the maximally exposed individual (MEI) for the air pathway per Curie (Ci) of each radionuclide remaining in the combined FTF waste tanks. For the air pathway analysis, several gaseous radionuclides were considered. These included carbon-14 (C-14), chlorine-36 (Cl-36), iodine-129 (I-129), selenium-79 (Se-79), antimony-125 (Sb-125), tin-126 (Sn-126), tritium (H-3), and technetium-99 (Tc-99). The dose to the MEI was estimated at the SRS Boundary during the 100 year institutional control period. For the 10,000 year post closure compliance period, the dose to the MEI was estimated at the 100 m compliance point. Additionally, the dose to the MEI was estimated at a seepage outcrop located 1600 m from the facility. For the radon pathway analysis, five parent radionuclides and their progeny were analyzed. These parent radionuclides included uranium-238 (U-238), plutonium-238 (Pu-238), uranium-234 (U-234), thorium-230 (Th-230), and radium-226 (Ra-226). The peak flux of radon-222 due to each parent radionuclide was estimated for the simulation period of 10,100 years.

  8. Evaluation of the diffuse contamination of soils caused by residues coming from the large scale production of phosphate fertilisers

    NASA Astrophysics Data System (ADS)

    Martinez, M. J.; Perez-Sirvent, C.; Martinez-Lopez, S.; Bolivar, J. P.; Mosqueda, F.; Vaca, F.; Garcia-Tenorio, R.

    2012-04-01

    The obtaining of phosphate fertilizers results in large amounts of residues that are frequently accumulated in deposits or pools occupying a wide area. These residues are acidic, and contain variable amounts of trace elements and radionuclides. The potentially polluting agents can be leached by rainwater, and so transferred to the surface waters and then to the groundwater after soil infiltration. Since the distribution and thickness of the residue deposits are variable, the contaminants cannot be easily traced back to a single, well defined source, and so a diffuse contamination (nonpoint source pollution) of the surrounding soils and waters occurs. This communication reports the results obtained in the study of soils close to the phosphogypsum deposits placed near Rio Tinto (Huelva, Spain). The zone is affected not only by the mentioned residues but also by the tides due to the vicinity of the sea. The samples studied had a low organic content and a low acidity with average values of 30 mS/cm for the EC. The mineralogical study allowed illite, goethite, quartz, gypsum and kaolinite to be identified as the main mineralogical components. Although the arsenic level was relatively high (about 600 mg/Kg) the data proved that this element is not mobilized into water. Analytical data for 238U , 234U, 235U, 228Th, 230Th, 232Th, 226Ra, 228Ra, 210Po, 40K , 137Cs were also obtained.

  9. An accurate method to measure alpha-emitting natural radionuclides in atmospheric filters: Application in two NORM industries

    NASA Astrophysics Data System (ADS)

    Lozano, R. L.; Bolívar, J. P.; San Miguel, E. G.; García-Tenorio, R.; Gázquez, M. J.

    2011-12-01

    In this work, an accurate method for the measurement of natural alpha-emitting radionuclides from aerosols collected in air filters is presented and discussed in detail. The knowledge of the levels of several natural alpha-emitting radionuclides (238U, 234U, 232Th, 230Th, 228Th, 226Ra and 210Po) in atmospheric aerosols is essential not only for a better understanding of the several atmospheric processes and changes, but also for a proper evaluation of the potential doses, which can inadvertently be received by the population via inhalation. The proposed method takes into account the presence of intrinsic amounts of these radionuclides in the matrices of the quartz filters used, as well as the possible variation in the humidity of the filters throughout the collection process. In both cases, the corrections necessary in order to redress these levels have been evaluated and parameterized. Furthermore, a detailed study has been performed into the optimisation of the volume of air to be sampled in order to increase the accuracy in the determination of the radionuclides. The method as a whole has been applied for the determination of the activity concentrations of U- and Th-isotopes in aerosols collected at two NORM (Naturally Occurring Radioactive Material) industries located in the southwest of Spain. Based on the levels found, a conservative estimation has been performed to yield the additional committed effective doses to which the workers are potentially susceptible due to inhalation of anthropogenic material present in the environment of these two NORM industries.

  10. Generic performance assessment for a deep repository for low and intermediate level waste in the UK--a case study in assessing radiological impacts on the natural environment.

    PubMed

    Jones, S R; Patton, D; Copplestone, D; Norris, S; O'Sullivan, P

    2003-01-01

    Concentrations of radionuclides in soil and surface water, taken from a generic performance assessment of a repository for low and intermediate level radioactive waste, assumed to be located in the UK, have been used as the basis for a case study in assessing radiological impacts on the natural environment. Simplified descriptions of the terrestrial and aquatic ecosystem types likely to be impacted have been developed. A scoping assessment has identified (226)Ra, (210)Po, (234)U, (230)Th and (238)U as having the highest potential for impact, with doses from internally incorporated alpha emitters as being potentially of particular importance. These nuclides, together with (36)Cl and (129)I (which have proved to be of importance in radiological risk assessments for humans) were included in a more detailed dose assessment. A basic methodology for dose assessment of ecosystems is described, and has been applied for the defined impacted ecosystems. Paucity of published data on concentration factors prevented a more detailed assessment for terrestrial ecosystems. For the aquatic ecosystem, a more detailed assessment was possible and highest calculated absorbed dose rates (weighted for the likely higher biological effectiveness of alpha radiation) were about 6.5 microGy h(-1). We conclude that harm to the impacted ecosystems is unlikely and make the observation that the lack of concentration factor or transfer factor data for a sufficiently wide range of species, ecosystems and nuclides appears to be the principal obstacle to establishing a comprehensive framework for the application of radiological protection to ecosystems.

  11. Measurements of cross sections and decay properties of the isotopes of elements 112, 114, and 116 produced in the fusion reactions {sup 233,238}U, {sup 242}Pu, and {sup 248}Cm+{sup 48}Ca

    SciTech Connect

    Oganessian, Yu.Ts.; Utyonkov, V.K.; Lobanov, Yu.V.; Abdullin, F.Sh.; Polyakov, A.N.; Shirokovsky, I.V.; Tsyganov, Yu.S.; Gulbekian, G.G.; Bogomolov, S.L.; Gikal, B.N.; Mezentsev, A.N.; Iliev, S.; Subbotin, V.G.; Sukhov, A.M.; Voinov, A.A.; Buklanov, G.V.; Subotic, K.; Zagrebaev, V.I.; Itkis, M.G.; Patin, J.B.

    2004-12-01

    We have studied the dependence of the production cross sections of the isotopes {sup 282,283}112 and {sup 286,287}114 on the excitation energy of the compound nuclei {sup 286}112 and {sup 290}114. The maximum cross section values of the xn-evaporation channels for the reaction {sup 238}U({sup 48}Ca,xn){sup 286-x}112 were measured to be {sigma}{sub 3n}=2.5{sub -1.1}{sup +1.8} pb and {sigma}{sub 4n}=0.6{sub -0.5}{sup +1.6} pb; for the reaction {sup 242}Pu({sup 48}Ca,xn){sup 290-x}114: {sigma}{sub 2n}{approx}0.5 pb, {sigma}{sub 3n}=3.6{sub -1.7}{sup +3.4} pb, and {sigma}{sub 4n}=4.5{sub -1.9}{sup +3.6} pb. In the reaction {sup 233}U({sup 48}Ca,2-4n){sup 277-279}112 at E*=34.9=2.2 MeV we measured an upper cross section limit of {sigma}{sub xn}{<=}0.6 pb. The observed shift of the excitation energy associated with the maximum sum evaporation residue cross section {sigma}{sub ER}(E*) to values significantly higher than that associated with the calculated Coulomb barrier can be caused by the orientation of the deformed target nucleus in the entrance channel of the reaction. An increase of {sigma}{sub ER} in the reactions of actinide targets with {sup 48}Ca is consistent with the expected increase of the survivability of the excited compound nucleus upon closer approach to the closed neutron shell N=184. In the present work we detected 33 decay chains arising in the decay of the known nuclei {sup 282}112, {sup 283}112, {sup 286}114, {sup 287}114, and {sup 288}114. In the decay of {sup 287}114({alpha}){yields}{sup 283}112({alpha}){yields}{sup 279}110(SF), in two cases out of 22, we observed decay chains of four and five sequential {alpha} transitions that end in spontaneous fission of {sup 271}Sg (T{sub {alpha}}{sub /SF}=2.4{sub -1.0}{sup +4.3} min) and {sup 267}Rf (T{sub SF}{approx}2.3 h), longer decay chains than reported previously. We observed the new nuclide {sup 292}116 (T{sub {alpha}}=18{sub -6}{sup +16} ms,E{sub {alpha}}=10.66{+-}0.07 MeV) in the irradiation of the

  12. Estimation of ground water residence times in the Critical zone: insight from U activity ratios

    NASA Astrophysics Data System (ADS)

    Chabaux, Francois; Ackerer, Julien; Lucas, Yann; viville, Daniel

    2016-04-01

    The use of radioactive disequilibria as tracers and chronometers of weathering processes and related mass transfers has been recognized since the 60'. The development, over the last two decades, of analytical methods for measuring very precisely U-series nuclides (especially, 234U, 230Th and 226Ra) in environmental samples has opened up new scientific applications in Earth Surface Sciences. Here, we propose to present the potential of U activity ratios in surface waters as chronometer of water transfers at a watershed scale. This will be illustrated from studies performed at different scales, with the analysis of U activity ratios in surface waters from small watersheds (Strengbach and Ringelbach watersheds in the Vosges Mountain, France) but also from watersheds of much more regional extension (e.g., the Upper Rhine basin or the Ganges basin). These various studies show that variations of U activity ratios in surface waters are mainly associated with 234U-238U fractionations occurring during the water transfer within the bedrock, which intensity depends on two main parameters: the petro-physical characteristics of the aquifer, principally the geometry of water-rock interfaces and the duration of the water-rock interactions. This readily explains why different U activity ratios (UAR) can be observed in the different aquifers of a continental hydrosystem and hence why UAR can be used to trace the source of river waters. For a hydrological system developed on a substratum marked by fairly homogeneous petro-physical characteristics, the main parameter controlling the UAR in waters draining such a system would be the duration of the water-rock interactions. Variations of UAR in stream or spring waters of such a system can therefore be modeled using simple reactive transport model, which allows the estimation of both the dissolution rate of the bedrock and the residence time of the waters within the aquifer.

  13. Radiation Doses to Members of the U.S. Population from Ubiquitous Radionuclides in the Body: Part 1, Autopsy and In Vivo Data

    SciTech Connect

    Watson, David J.; Strom, Daniel J.

    2011-02-25

    This paper is part one of a three-part series investigating annual effective doses to residents of the United States from intakes of ubiquitous radionuclides, including radionuclides occurring naturally, radionuclides whose concentrations are technologically enhanced, and anthropogenic radionuclides. This series of papers explicitly excludes intakes from inhaling 222Rn, 220Rn, and their short-lived decay products; it also excludes intakes of radionuclides in occupational and medical settings. The goal of part one of this work was to review, summarize, and characterize all published and some unpublished data for U.S. residents on ubiquitous radionuclide concentrations in tissues and organs. Forty-five papers and reports were obtained and their data reviewed, and three data sets were obtained via private communication. The 45 radionuclides of interest are the 238U series (14 nuclides), the actinium series (headed by 235U; 11 nuclides), and the 232Th series (11 nuclides); primordial radionuclides 87Rb and 40 K; cosmogenic and fallout radionuclides 14C and 3H; and purely anthropogenic radionuclides 137Cs-137mBa, 129I, and 90Sr-90Y. Measurements judged to be relevant were available for only 15 of these radionuclides: 238U, 235U, 234U, 232Th, 230Th, 228Th, 228Ra, 226Ra, 210Pb, 210Po, 137Cs, 87Rb, 40K, 14C, and 3H. Recent and relevant measurements were not available for 129I and 90Sr-90Y. A total of 11,714 radionuclide concentration measurements were found in one or more tissues or organs from 14 States. Data on age, sex, geographic locations, height, and weight of subjects were available only sporadically. Too often authors did not provide meaningful values of uncertainty of measurements so that variability in data sets is confounded with measurement uncertainty. The following papers detail how these shortcomings are overcome to achieve the goals of the three-part series.

  14. Rapid method for the determination of 226Ra in hydraulic fracturing wastewater samples

    SciTech Connect

    Maxwell, Sherrod L.; Culligan, Brian K.; Warren, Richard A.; McAlister, Daniel R.

    2016-03-24

    A new method that rapidly preconcentrates and measures 226Ra from hydraulic fracturing wastewater samples was developed in the Savannah River Environmental Laboratory. The method improves the quality of 226Ra measurements using gamma spectrometry by providing up to 100x preconcentration of 226Ra from this difficult sample matrix, which contains very high levels of calcium, barium, strontium, magnesium and sodium. The high chemical yield, typically 80-90%, facilitates a low detection limit, important for lower level samples, and indicates method ruggedness. Ba-133 tracer is used to determine chemical yield and correct for geometry-related counting issues. The 226Ra sample preparation takes < 2 hours.

  15. Radiological Impact of Phosphogypsum Application in Agriculture

    SciTech Connect

    Dias, Nivea M. P.; Caires, Eduardo F.; Pires, Luiz F.; Bacchi, Marcio A.; Fernandes, Elisabete A. N.

    2010-08-04

    Phosphogypsum (PG) contains radionuclides from {sup 238}U and {sup 232}Th decay series. Due to the presence of these radionuclides, many countries restricted the use of PG in agriculture, however there is not such restriction in Brazil. The main objective of this work was to evaluate the impact of PG application on {sup 226}Ra ({sup 238}U) and {sup 228}Ra ({sup 232}Th) concentrations in soil. Gamma-spectrometry was carried out using HPGe detector. No increment of {sup 226}Ra and {sup 228}Ra was observed for increasing PG doses. Average values found for {sup 226}Ra and {sup 228}Ra were respectively 37 Bq kg{sup -1} and 57 Bq kg{sup -1}. The results showed that the increasing PG doses in the specific conditions of the experiment did not cause a significant increment of radionuclides.

  16. Radiological Impact of Phosphogypsum Application in Agriculture

    NASA Astrophysics Data System (ADS)

    Dias, Nivea M. P.; Caires, Eduardo F.; Pires, Luiz F.; Bacchi, Marcio A.; Fernandes, Elisabete A. N.

    2010-08-01

    Phosphogypsum (PG) contains radionuclides from 238U and 232Th decay series. Due to the presence of these radionuclides, many countries restricted the use of PG in agriculture, however there is not such restriction in Brazil. The main objective of this work was to evaluate the impact of PG application on 226Ra (238U) and 228Ra (232Th) concentrations in soil. Gamma-spectrometry was carried out using HPGe detector. No increment of 226Ra and 228Ra was observed for increasing PG doses. Average values found for 226Ra and 228Ra were respectively 37 Bq kg-1 and 57 Bq kg-1. The results showed that the increasing PG doses in the specific conditions of the experiment did not cause a significant increment of radionuclides.

  17. A Record of Uranium-Series Transport in Fractured, Unsaturated Tuff at Nopal I, Sierra Peña Blanca, Chihuahua, Mexico

    NASA Astrophysics Data System (ADS)

    Denton, J.; Goldstein, S. J.; Paviet, P.; Nunn, A. J.; Amato, R. S.; Hinrichs, K. A.

    2015-12-01

    In this study we utilize U-series disequilibria measurements to investigate mineral fluid interactions and the role fractures play in the geochemical evolution of an analogue for a high level nuclear waste repository, the Nopal I uranium ore deposit. Samples of fracture-fill materials have been collected from a vertical drill core and surface fractures. High uranium concentrations in these materials (12-7700 ppm) indicate U mobility and transport from the deposit in the past. U concentrations generally decrease with horizontal distance away from the ore deposit but show no trend with depth. Isotopic activity ratios indicate a complicated geochemical evolution in terms of the timing and extent of actinide mobility, possibly due to changing environmental (redox) conditions over the history of the deposit. 234U/238U activity ratios are generally distinct from secular equilibrium and indicate some degree of open system U behavior during the past 1.2 Ma. However, calculated closed system 238U-234U-230Th model ages are generally >313 ka and >183 ka for the surface fracture and drill core samples respectively, suggesting closed system behavior for U and Th over this most recent time period. Whole rock isochrons drawn for the drill core samples show that at two of three depths fractures have remained closed with respect to U and Th mobility for >200 ka. However, open system behavior for U in the last 350 ka is suggested at 67 m depth. 231Pa/235U activity ratios within error of unity suggest closed system behavior for U and Pa for at least the past 185 ka. 226Ra/230Th activity ratios are typically <1 (0.7-1.2), suggesting recent (<8 ka) radium loss and mobility due to ongoing fluid flow in the fractures. Overall, the mainly closed system behavior of U-Th-Pa over the past ~200 ka provides one indicator of the geochemical immobility of these actinides over long time-scales for potential nuclear waste repositories sited in fractured, unsaturated tuff.

  18. Geochemistry of uranium and thorium and natural radioactivity levels of the western Anatolian plutons, Turkey

    NASA Astrophysics Data System (ADS)

    Papadopoulos, Argyrios; Altunkaynak, Şafak; Koroneos, Antonios; Ünal, Alp; Kamaci, Ömer

    2017-01-01

    Seventy samples from major plutons (mainly granitic) of Western Anatolia (Turkey) have been analyzed by γ-ray spectrometry to determine the specific activities of 238U, 226Ra, 232Th and 40K (Bq/kg). Τhe natural radioactivity ranged up to 264 Bq/kg for 238U, 229.62 Bq/kg for 226Ra, up to 207.32 Bq/kg for 232Th and up to 2541.95 Bq/kg for 40K. Any possible relationship between the specific activities of 226Ra, 238U, 232Th and 40K and some characteristics of the studied samples (age, rock-type, colour, grain size, occurrence, chemical and mineralogical composition) was investigated. Age, major and trace element geochemistry, color, pluton location and mineralogical composition are likely to affect the concentrations of the measured radionuclides. The range of the Th/U ratio was large (0.003-11.374). The latter, along with 226Ra/238U radioactive secular disequilibrium, is also discussed and explained by magmatic processes during differentiation.

  19. Precise determination of U isotopic compositions in low concentration carbonate samples by MC-ICP-MS.

    PubMed

    Wang, Ruo-Mei; You, Chen-Feng

    2013-03-30

    We developed a fast and simple analytical procedure for precise determination of U isotopic compositions in low concentration natural samples. The main advantage of the new method is that it requires only 12ng U and can obtain all U isotopic ratios without using spike. Five carbonate reference materials (JCp-1, RKM-4, RKM-5, GBW04412 and GBW04413) and 3 international standards with different matrices (IAPSO, IRMM-3184 and CRM-U010) were analyzed for ((234)U/(238)U) and (238)U/(235)U ratios by MC-ICPMS. Using our method, the results for these standards are in close agreement with the certified values, 1.144 ± 0.004, 0.966 ± 0.004 and 0.990 ± 0.003 for ((234)U/(238)U) and 137.72 ± 0.13, 137.64 ± 0.15 and 98.63 ± 0.04 for (238)U/(235)U, in IAPSO, IRMM-3184 and CRM-U010, respectively. The long-term reproducibility of ((234)U/(238)U) and (238)U/(235)U is 0.970 ± 0.002 and 137.56 ± 0.09; 1.144 ± 0.004 and 137.72 ± 0.13, respectively, for in-house U solution and IAPSO. The new ((234)U/(238)U) results for carbonates show much better precision than previous studies and also reflect their age variability. The obtained (238)U/(235)U ratios, representing the first measurements in these carbonate specimens, are rather constant. The method described here requires only 12 ng of U for analysis and can be completed in 5.2 min. The approach provides a fast method to measure ((234)U/(238)U) and (238)U/(235)U ratios in sample matrices commonly encountered in studies of chemical weathering, oceanography and paleoclimatology.

  20. Uranium-thorium series radionuclides in brines and reservoir rocks from two deep geothermal boreholes in the Salton Sea Geothermal Field, southeastern California

    NASA Astrophysics Data System (ADS)

    Zukin, Jeffrey G.; Hammond, Douglas E.; Teh-Lung, Ku; Elders, Wilfred A.

    1987-10-01

    Naturally occurring U and Th series radionuclides have been analyzed in high temperature brines (~300°C, 25 wt% dissolved solids) and associated rocks from two deep geothermal wells located on the northeastern margin of the Salton Sea Geothermal Field (SSGF). These data are part of a study of the SSGF as a natural analog of possible radionuclide behavior near a nuclear waste repository constructed in salt beds, and permit evaluation of some characteristics of water-rock interaction in the SSGF. Rock/Brine concentration ratios ( Rc = (dpm/ g) rock/(dpm/ g) brine) were found to vary from near unity for isotopes of Ra, Pb and Rn to about 5 × 10 5 for 232Th. The high sorptivity of 232Th is closely followed by that of 238U and 234U ( Rc ~ 5 × 10 4), suggesting that U is retained in the +4 oxidation state by the reducing conditions in the brines. The relatively high solubility of 210Pb and 212Pb is attributed to formation of chloride complexes, while the high Ra solubility is attributed to chloride complexing, a lack of suitable adsorption sites due to the high brine salinity and temperature, and the reducing conditions that prevent MnO 2 and RaSO 4 from forming. The 228Ra /226Ra ratios in the brines are approximately equal to those of their parents ( 232Th /230Th ) in associated rocks, indicating that Ra equilibration in the brine-rock system is achieved within the mean life of 228Ra (8.3 years). The 224Ra /228Ra ratios in these brines are about 0.7, indicating that either (1) brine composition is not homogeneous and 224Ra decays in fracture zones deficient in Ra and Th as the brine travels to the wellhead or (2) Ra equilibration in the brine-host rock system is not complete within the mean life of 224Ra (5.2 days) because the desorption of 224Ra from the solid phase is impeded. The 228Ac /228Ra activity ratio in the SSGF brines studied is <0.1, and from this ratio the residence time of 228Ac in the brine before sorption onto solid surfaces is estimated to be <70

  1. Direct determination of radionuclides in building materials with self-absorption correction for the 63 and 186 keV γ-energy lines.

    PubMed

    Długosz-Lisiecka, Magdalena; Ziomek, Martyna

    2015-12-01

    The use of 911 keV and 129 keV γ-line intensity ratio has been applied for self-absorption correction of the 63 keV (234)Th ((238)U) and 186 keV((226)Ra and (235)U) lines in typical building materials and soil samples. Proposed procedure allows to determine (238)U from the (234)Th line (63 keV) and (226)Ra after subtraction of (235)U interference in the 186 keV. It is important in the case of low uranium concentration and weak intensity of (235)U 143 keV γ energy line, when activity of this radionuclide can be apprised on the natural constant (238)U/(235)U ratio, only (excluding accidental anthropogenic depleted uranium deposition in the soil samples). Therefore, by this method a direct and fast determination of the (226)Ra and other important radionuclides, without one month waiting period for (226)Ra-(222)Rn daughter equilibrium, is possible. The accuracy of the method has been confirmed (relative relation deviation <10%) for typical buildings materials such as: tales, bricks, concrete blocks and various type of ceramic materials.

  2. Testing the concept of drift shadow at Yucca Mountain, Nevada

    USGS Publications Warehouse

    Paces, J.B.; Neymark, L.A.; Ghezzehei, T.; Dobson, P.F.

    2006-01-01

    If proven, the concept of drift shadow, a zone of reduced water content and slower ground-water travel time beneath openings in fractured rock of the unsaturated zone, may increase performance of a proposed geologic repository for high-level radioactive waste at Yucca Mountain, To test this concept under natural-flow conditions present in the proposed repository horizon, isotopes within the uranium-series decay chain (uranium-238, uranium-234, and thorium-230, or 238U-234U-230Th) have been analyzed in samples of rock from beneath four naturally occurring lithophysal cavities. All rock samples show 234U depletion relative to parent 238U indicating varying degrees of water-rock interaction over the past million years. Variations in 234U/238U activity ratios indicate that depletion of 234U relative to 238U can be either smaller or greater in rock beneath cavity floors relative to rock near cavity margins. These results are consistent with the concept of drift shadow and with numerical simulations of meter-scale spherical cavities in fractured tuff. Differences in distribution patterns of 234U/ 238U activity ratios in rock beneath the cavity floors are interpreted to reflect differences in the amount of past seepage into lithophysal cavities, as indicated by the abundance of secondary mineral deposits present on the cavity floors.

  3. Testing the Concept of Drift Shadow at Yucca Mountain, Nevada

    SciTech Connect

    J.B. Paces; L.A. Neymark; T. Ghezzehei; P.F. Dobson

    2006-03-10

    If proven, the concept of drift shadow, a zone of reduced water content and slower ground-water travel time beneath openings in fractured rock of the unsaturated zone, may increase performance of a proposed geologic repository for high-level radioactive waste at Yucca Mountain. To test this concept under natural-flow conditions present in the proposed repository horizon, isotopes within the uranium-series decay chain (uranium-238, uranium-234, and thorium-230, or {sup 238}U-{sup 234}U-{sup 230}Th) have been analyzed in samples of rock from beneath four naturally occurring lithophysal cavities. All samples show {sup 234}U depletion relative to parent {sup 238}U, indicating varying degrees of water-rock interaction over the past million years. Variations in {sup 234}U/{sup 238}U activity ratios indicate that depletion of {sup 234}U relative to {sup 238}U can be either smaller or greater in rock beneath cavity floors relative to rock near cavity margins. These results are consistent with the concept of drift shadow and with numerical simulations of meter-scale spherical cavities in fractured tuff. Differences in distribution patterns of {sup 234}U/{sup 238}U activity ratios in rock beneath the cavity floors are interpreted to reflect differences in the amount of past seepage into lithophysal cavities, as indicated by the abundance of secondary mineral deposits present on the cavity floors.

  4. Lichens and mosses as polonium and uranium biomonitors on Sobieszewo Island.

    PubMed

    Boryło, Alicja; Romańczyk, Grzegorz; Skwarzec, Bogdan

    2017-01-01

    In the study the activities of polonium (210)Po and uranium (234)U, (238)U radionuclides in moss and lichen samples were determined using the alpha spectrometry. Different lichens and mosses were collected around the Sobieszewo Island (northern Poland) and investigated for potential use as biomonitors for (210)Po and (238)U deposition. Mosses and lichens have a high efficiency in capturing (210)Po and (238)U from atmospheric fallout. The obtained results showed that (210)Po, (238)U concentrations are changing in analyzed thallophytes samples depending on the type of thallus.

  5. U-Sr isotopic speedometer: Fluid flow and chemical weatheringrates inaquifers

    SciTech Connect

    Maher, Kate; DePaolo, Donald J.; Christensen, John N.

    2005-12-27

    Both chemical weathering rates and fluid flow are difficultto measure in natural systems. However, these parameters are critical forunderstanding the hydrochemical evolution of aquifers, predicting thefate and transport of contaminants, and for water resources/water qualityconsiderations. 87Sr/86Sr and (234U/238U) activity ratios are sensitiveindicators of water-rock interaction, and thus provide a means ofquantifying both flow and reactivity. The 87Sr/86Sr values in groundwaters are controlled by the ratio of the dissolution rate to the flowrate. Similarly, the (234U/238U) ratio of natural ground waters is abalance between the flow rate and the dissolution of solids, andalpha-recoil loss of 234U from the solids. By coupling these two isotopesystems it is possible to constrain both the long-term (ca. 100's to1000's of years) flow rate and bulk dissolution rate along the flow path.Previous estimates of the ratio of the dissolution rate to theinfiltration flux from Sr isotopes (87Sr/86Sr) are combined with a modelfor (234U/238U) to constrain the infiltration flux and dissolution ratefor a 70-m deep vadose zone core from Hanford, Washington. The coupledmodel for both (234U/238U) ratios and the 87Sr/86Sr data suggests aninfiltration flux of 5+-2 mm/yr, and bulk silicate dissolution ratesbetween 10-15.7 and 10-16.5 mol/m2/s. The process of alpha-recoilenrichment, while primarily responsible for the observed variation in(234U/238U) of natural systems, is difficult to quantify. However, therate of this process in natural systems affects the interpretation ofmost U-series data. Models for quantifying the alpha-recoil loss fractionbased on geometric predictions, surface area constraints, and chemicalmethods are also presented. The agreement between the chemical andtheoretical methods, such as direct measurement of (234U/238U) of thesmall grain size fraction and geometric calculations for that sizefraction, is quite good.

  6. Uranium-234 anomalies in corals older than 150,000 years

    SciTech Connect

    Bard, E. Columbia Univ., Palisades, NY ); Fairbanks, R.G.; Zindler, A. ); Hamelin, B. Univ. Aix-Marseille III ); Hoang, C.T. )

    1991-08-01

    The authors present new precise U-Th ages of well-preserved coral specimens collected from the island of Barbados, West Indies, and the atoll of Mururoa, French Polynesia. Their new data confirm the ages attributed to oxygen isotope stage 7 in the framework of the Milankovitch theory. By using thermal ionization mass spectrometry (TIMS), it is also possible to quantify precisely the [sup 234]U/[sup 238]U ratios in corals. Samples older than 150 kyr B.P. are shown to be characterized by significant excesses of [sup 234]U relative to the uranium isotopic composition expected if the corals grew in present-day sea water. Assuming that the [sup 230]Th-ingrowth ages are accurate, these anomalies translate into high initial [sup 234]U/[sup 238]U ratios: about 1.2 at 200 kyr and up to 1.5 at about 450 kyr B.P. They propose that the anomalies result from both diagenetic addition and replacement of U and possibly from global changes in the [sup 234]U/[sup 238]U composition of the sea water through time. The [sup 234]U anomalies cast doubt on the accuracy of the classical [sup 230]Th-ingrowth dating method in old corals, and in particular for the use of measured [sup 234]U/[sup 238]U ratios alone to date corals older than 150 kyr.

  7. Impact of vegetation change on the mobility of uranium- and thorium-series nuclides in soils

    NASA Astrophysics Data System (ADS)

    Gontier, A.; Rihs, S.; Turpault, M.-P.; Chabaux, F.

    2012-04-01

    The effect of land cover change on chemical mobility and soil response was investigated using short- and long-lived nuclides from the U- and Th series. Indeed, the matching of these nuclides half-live to the pedogenic processes rates make these nuclides especially suitable to investigate either time or mechanism of transfers within a soil-water-plant system. This study was carried out from the experimental Breuil-Chenue site (Morvan mountains, France). The native forest (150 year-old) was partially clear-felled and replaced in 1976 by mono-specific plantations distributed in different stands. Following this cover-change, some mineralogical changes in the acid brown soil were recognized (Mareschal, 2008). Three soil sections were sampled under the native forest and the replanted oak and Douglas spruce stands respectively. The (238U), (234U), (230Th), (226Ra), (232Th) and (228Ra) activities were analysed by thermal ionization mass spectrometry (TIMS), inductively coupled plasma mass spectrometry (MC-ICPMS) and gamma spectrometry. Significant differences in U, Th, and Ra activities were observed between the soils located under the native forest or the replanted-trees stands, mostly dominated by a large uranium mobilization from the replanted soils. Moreover, all the investigated U and Th-series activity ratios show a contrasted trend between the shallowest horizons (0-50cm) and the deepest one (below 50cm), demonstrating the chemical effect of the vegetation change on the shallow soil layers. Using a continuous open-system leaching model, the coupled radioactive disequilibria measured in the different soil layers permit to quantify the rate of the radionuclides mobilities. Reference: Mareschal, L., 2008. Effet des substitutions d'essences forestières sur l'évolution des sols et de leur minéralogie : bilan après 28 ans dans le site expérimental de Breuil (Morvan) Université Henri Poincaré, Nancy-I.

  8. Natural attenuation reactions at a uranium mill tailings site, western U.S.A.

    PubMed

    Zhu, Chen; Anderson, Greg M; Burden, David S

    2002-01-01

    This paper presents a modeling analysis of the geochemical evolution of a contaminated sandy aquifer at a uranium mill tailings site in the western United States. The tailings pond contains fluids having a pH of 1.5 to 3.5 and high levels of As, Be, Cd, Cr, Pb, Mo, Ni, Se, 226Ra, 228Ra, 230Th, 238U, and 234U. Seepage of tailings fluids into the aquifer has formed a low-pH ground water plume. The reclamation plan is to install a low-permeability cover on the tailings pond to stop the seepage and allow the plume to be attenuated by reactions with the aquifer matrix and flushed by uncontaminated upgradient ground water. To evaluate this reclamation scenario, ground water and sediment core samples were analyzed along one flowpath. Speciation-solubility and mass-transfer modeling revealed two sets of chemical reactions for acid seepage and flushing, respectively. The current concentrations and distribution of ground water constituents can be interpreted as being controlled by stepwise pH-buffer reactions with calcite, amorphous aluminum hydroxide, and amorphous iron hydroxides. These buffer reactions divide the aquifer into zones of near-constant pH, separated by interface zones. For the flushing stage, it is predicted that reactions with surface-bound species will dominate the reaction paths, and more pore volumes are required to neutralize the plume than predicted by models that do not consider surface reactions. Direct mineralogical and surface analysis is needed to substantiate this assertion.

  9. Behaviour and mobility of U and Ra in sediments near an abandoned uranium mine, Cornwall, UK.

    PubMed

    Siddeeg, Saifeldin M; Bryan, Nicholas D; Livens, Francis R

    2015-01-01

    Sediment samples were collected from the vicinity of the abandoned South Terras uranium mine in south-west UK and analysed for uranium and (226)Ra to explore their geochemical dispersion. The radioactivity concentrations in the sediment samples were measured using alpha spectrometry for uranium, and gamma spectrometry for radium. Sequential chemical extraction was applied to selected sediments in order to investigate the speciation of the radionuclides and their association with stable elements. The activity ratio of the uranium isotopes was used to explore the mobility of uranium, and scanning electron microscopy (SEM) and electron microprobe analysis (EMPA) were used to characterise the sediments. The radiochemical results identified two locations with enhanced radioactivity, so two samples from these locations were further investigated. The geochemical distribution of the radionuclides in these two samples varies within the five operationally-defined fractions. In one sample, the majority of the uranium was released from the 'carbonate' fraction, followed by the organic fractions. Similarly, in the second sample, the uranium was mainly resealed from the carbonate fraction, although a considerable percentage associated with the resistant fraction. The fractionation trend of radium noticed to show some similarities to that of barium, as expected from the similarity in their chemistries. Geochemical distributions of the stable elements, such as Mn, Ti and As, were different in the enhanced radioactivity samples. The activity ratio of (234)U/(238)U shows different trends in the two sediments, signifying the impact of organic matter and/or the exchange between water and sediment. SEM and EMPA analysis identified uranium-bearing phases in association with potassium, calcium, iron, manganese and arsenic.

  10. Radionuclides transfer into halophytes growing in tidal salt marshes from the Southwest of Spain.

    PubMed

    Luque, Carlos J; Vaca, Federico; García-Trapote, Ana; Hierro, Almudena; Bolívar, Juan P; Castellanos, Eloy M

    2015-12-01

    Estuaries are sinks of materials and substances which are released directly into them or transported from rivers that drain the basin. It is usual to find high organic matter loads and fine particles in the sediments. We analyzed radionuclide concentrations ((210)Po, (230)Th, (232)Th, (234)U, (238)U, (226)Ra, (228)Th, (228)Ra, (40)K) in sediments and three different organs (roots, stems and leaves) of three species of halophytes plants (Spartina maritima, Spartina densiflora and Sarcocornia perennis). The study was carried out in two tidal salt marshes, one polluted by U-series radionuclides and another nearby that was unpolluted and was used as a control (or reference) area. The Tinto River salt marsh shows high levels of U-series radionuclides coming from mining and industrial discharges. On the contrary, the unperturbed Piedras River salt marsh is located about 25 km from the Tinto marsh, and shows little presence of contaminants and radionuclides. The results of this work have shown that natural radionuclide concentrations (specially the U-isotopes) in the Tinto salt marsh sediments are one order of magnitude higher than those in the Piedras marsh. These radionuclide enhancements are reflected in the different organs of the plants, which have similar concentration increases as the sediments where they have grown. Finally, the transfer factor (TF) of the most polluted radionuclides (U-isotopes and (210)Po) in the Tinto area are one order of magnitude higher than in the Piedras area, indicating that the fraction of each radionuclide in the sediment originating from the pollution is more available for the plants than the indigenous fraction. This means that the plants of the salt marshes are unhelpful as bioindicators or for the phytoremediation of radionuclides.

  11. Geochemical investigations by the U.S. Geological Survey on uranium mining, milling, and environmental restoration

    USGS Publications Warehouse

    Landa, Edward R.; Cravotta, Charles A.; Naftz, David L.; Verplanck, Philip L.; Nordstrom, D. Kirk; Zielinski, Robert A.

    2000-01-01

    Recent research by the U.S. Geological Survey has characterized contaminant sources and identified important geochemical processes that influence transport of radionuclides from uranium mining and milling wastes. 1) Selective extraction studies indicated that alkaline earth sulfates and hydrous ferric oxides are important hosts of 226Ra in uranium mill tailings. The action of sulfate-reducing and ironreducing bacteria on these phases was shown to enhance release of radium, and this adverse result may temper decisions to dispose of uranium mill tailings in anaerobic environments. 2) Field studies have shown that although surface-applied sewage sludge/wood chip amendments aid in revegetating pyritic spoil, the nitrogen in sludge leachate can enhance pyrite oxidation, acidification of groundwater, and the consequent mobilization of metals and radionuclides. 3) In a U.S. Environmental Protection Agencyfunded study, three permeable reactive barriers consisting of phosphate-rich material, zero-valent iron, or amorphous ferric oxyhydroxide have been installed at an abandoned uranium upgrader facility near Fry Canyon, UT. Preliminary results indicate that each of the permeable reactive barriers is removing the majority of the uranium from the groundwater. 4) Studies on the geochemistry of rare earth elements as analogues for actinides such as uranium and thorium in acid mine drainage environments indicate high mobility under acid-weathering conditions but measurable attenuation associated with iron and aluminum colloid formation. Mass balances from field and laboratory studies are being used to quantify the amount of attenuation. 5) A field study in Colorado demonstrated the use of 234U/238U isotopic ratio measurements to evaluate contamination of shallow groundwater with uranium mill effluent.

  12. Fluxes of metals to a manganese nodule: Radiochemical, chemical, structural, and mineralogical studies

    USGS Publications Warehouse

    Moore, W.S.; Ku, T.-L.; Macdougall, J.D.; Burns, V.M.; Burns, R.; Dymond, J.; Lyle, M.W.; Piper, D.Z.

    1981-01-01

    Fluxes of metals to the top and bottom surfaces of a manganese nodule were determined by combining radiochemical (230Th, 231Pa, 232Th, 238U, 234U) and detailed chemical data. The top of the nodule had been growing in its collected orientation at 4.7 mm Myr-1 for at least 0.5 Myr and accreting Mn at 200 ??g cm-2 kyr-1. The bottom of the nodule had been growing in its collected orientation at about 12 mm Myr-1 for at least 0.3 Myr and accreting Mn at about 700 ??g cm-2 yr-1. Although the top of the nodule was enriched in iron relative to the bottom, the nodule had been accreting Fe 50% faster on the bottom. 232Th was also accumulating more rapidly in the bottom despite a 20-fold enrichment of 230Th on the top. The distribution of alpha-emitting nuclides calculated from detailed radiochemical measurements matched closely the pattern revealed by 109-day exposures of alpha-sensitive film to the nodule. However, the shape and slope of the total alpha profile with depth into the nodule was affected strongly by 226Ra and 222Rn migrations making the alpha-track technique alone an inadequate method of measuring nodule growth rates. Diffusion of radium in the nodule may have been affected by diagenetic reactions which produce barite, phillipsite and todorokite within 1 mm of the nodule surface; however, our sampling interval was too broad to document the effect. We have not been able to resolve the importance of nodule diagenesis on the gross chemistry of the nodule. ?? 1981.

  13. Natural radioactivity and radiological hazard assessment of Egyptian oil ashes.

    PubMed

    Mohammed, Hesham; Sadeek, Sadeek; Mahmoud, Abu Rehab; Diab, Hanan; Zaky, Doaa

    2016-08-01

    Oil fly and boiler ash samples were collected from the four major Egyptian power plants in order to determine their natural radioactivity. Secular equilibrium between (238)U and (232)Th and their decay products is significantly disturbed in oil ash samples. The (226)Ra/(238)U ratios were between 440 and 1993 with an average value of 801, indicating that the concentrations of daughters (226)Ra were very high compared to the parent (238)U in the oil ash samples. While, the average ratios for (210)Pb/(226)Ra in most samples were 1.19 ± 0.05, indicating a secular equilibrium in the (226)Ra-(210)Pb sub series. The natural radioactivity due to (238)U and (232)Th was found to be negligible. While the activity concentrations of (226)Ra ranged from 3205 to 12,320 Bq kg(-1) with an average value of 9284 Bq kg(-1), (210)Pb ranged from 5960 to 13,930 Bq kg(-1) with an average value of 11,513 Bq kg(-1). The results are compared with the reported data from other countries. The average value of radium equivalent activity was 9308 ± 2729 Bq kg(-1), while the external and internal hazard indexes were found to be 25 ± 7 and 50 ± 15, respectively. All the studied radiological parameters were higher than the recommended limit by the IAEA in all ash samples.

  14. Disequilibrium between uranium and its progeny in the Lake Issyk-Kul system (Kyrgyzstan) under a combined effect of natural and manmade processes.

    PubMed

    Gavshin, V M; Melgunov, M S; Sukhorukov, F V; Bobrov, V A; Kalugin, I A; Klerkx, J

    2005-01-01

    The Kadji-Sai abandoned field of U-bearing brown coal on the southern coast of Lake Issyk-Kul (Kyrgyzstan) poses a threat of radioactive pollution to the world's fifth deepest and second largest pristine highland lake. The valleys of ephemeral streams in the lake catchment are filled with coarse-grained sand and clay, with a background U--Ra activity of 35--55 Bqkg(-1). High activity areas vs. this background come from three sources: (1) scarce outcrops of uraniferous brown coal and mining wastes containing fragments of this coal with (238)U/(226)Ra ratios of 0.8 due to uranium losses through weathering; (2) manmade anomalies caused by a radioactive waste dump, where U was extracted from the ash of coal burnt at a coal-fired power plant. As a result, the (238)U/(226)Ra ratios become 0.15--0.25; (3) six catch pools terraced below the mine, where U activity decreases downslope, and (238)U/(226)Ra ratios reach 150--200. Uranium lost in the extraction process may have been retained on the terraces. The distribution pattern of radionuclides in the bottom sediments of the lake is controlled by water depth and offshore distance. The upper section of homogeneous limy--argillic deposits in the lake center remains undisturbed by currents, as indicated by regular sub-exponential distribution of atmospheric (137)Cs and (210)Pb(atm). Sedimentation rate in the lake center for the past century, found from (210)Pb, was 0.32 mmyr(-1). (238)U/(226)Ra in deep-water sediments was about 3. The activity of uranium adsorbed by sediments from the lake water was estimated by subtraction of the Ra-equilibrium component from the total U activity. Thus, the flux of dissolved U to the bottom sediments was as 2.07 x 10(-7)gcm(-2)yr(-1). The upper section of near-shore deposits was disturbed by currents, with (137)Cs and (210)Pb(atm) more or less uniformly distributed in this layer. Peaks of (226)Ra and (210)Pb occur at different depths from 5 to 20 cm below the sediment surface, with (238)U

  15. Localised magmatic constraints on continental back-arc volcanism in southern Mendoza, Argentina: the Santa Maria Volcano

    NASA Astrophysics Data System (ADS)

    Espanon, Venera R.; Chivas, Allan R.; Turner, Simon P.; Kinsley, Leslie P. J.; Dosseto, Anthony

    2016-11-01

    The Payún Matrú Volcanic Field constitutes part of the continental back-arc in Argentina. This volcanic field has been the focus of several regional investigations; however, geochemical analysis of recent volcanoes (<8 ka) at the scale of an individual volcano has not been conducted. We present a morphological description for the Santa Maria Volcano in addition to results from major and trace element analysis and 238U-230Th-226Ra disequilibria. The trace element evidence suggests that the Santa Maria magmatic source has a composition similar to that of the local intraplate end member (resembling an ocean island basalt-like source), with a slight contribution from subduction-related material. The U-series analyses suggest a high 226Ra excess over 230Th for this volcano, which is not derived from a shallow process such as hydrothermal alteration or upper crustal contamination. Furthermore, intermediate-depth processes such as fractional crystallisation have been inferred for the Santa Maria Volcano, but they are not capable of producing the 226Ra excess measured. The 226Ra excess is explained by deep processes like partial melting of mantle lithologies with some influence from subducted Chilean trench sediments. Due to the short half-life of 226Ra (1600 years), we infer that fast magma ascent rates are required to preserve the high 226Ra excess.

  16. The relationship between riverine U-series disequilibria and erosion rates in a basaltic terrain

    NASA Astrophysics Data System (ADS)

    Vigier, N.; Burton, K. W.; Gislason, S. R.; Rogers, N. W.; Duchene, S.; Thomas, L.; Hodge, E.; Schaefer, B.

    2006-09-01

    U-series isotopes have been measured in the dissolved phase, suspended load and bedload of the main rivers draining basaltic catchments in Iceland. For the dissolved phase, ( 234U/ 238U) and ( 238U/ 230Th) range between 1.08 and 2.2, and 7.4 and 516, respectively. For the suspended load and bedload, ( 234U/ 238U) and ( 238U/ 230Th) range from 0.97 to 1.09 and from 0.93 to 1.05, respectively. Chemical erosion rates, calculated from dissolved major elements, range between 13 and 333 t km - 2 yr - 1 . Physical erosion rates have also been estimated, from existing data, and range between 21 and 4864 t/km 2/yr, with an average of 519 t km - 2 yr - 1 . U-series disequilibria indicate that weathering in Iceland operates at close to steady-state conditions. A model of continuous weathering indicates a maximum weathering timescale of 10 kyr, with an average rate of uranium release into water of 1.6 · 10 - 4 yr - 1 , which is significant when compared to granitic terrains located at similar latitudes and to tropical basaltic terrains. All river waters display ( 234U/ 238U) greater than secular equilibrium, consistent with the effects of alpha-recoil. The same dissolved phase ( 234U/ 238U) exhibit a negative trend with physical erosion rates, explained by the dominant effect of close-to-congruent chemical weathering of hyaloclastites in the younger basaltic terrains. Therefore, chemical erosion rate and mineral weathering susceptibility play a major role in determining 234U- 238U disequilibria in basaltic river waters. Comparison of global data for river basins in which weathering was recently strongly limited indicates a negative correlation between silicate weathering rates estimated with major elements and the age of weathering estimated with U-series disequilibria. This strongly suggests a key role of time and soil thickness on the chemical erosion of silicates.

  17. Uranium contents and associated effective doses in drinking water from Biscay (Spain).

    PubMed

    Herranz, M; Abelairas, A; Legarda, F

    1997-06-01

    The determination of 234U and 238U content in drinking waters treated at four treatment plants supplying water to a set of municipalities located in northern Spain has given mean values of 1.14 mBq/L for 234U and 0.8 mBq/L for 238U. These contents, taking into account the population supplied with water and its distribution in age intervals, have allowed the determination of the annual intake of both radionuclides as well as the mean committed dose due to the ingestion of these radionuclides for which a value of 0.081 microSv/person is obtained.

  18. Radioactive characterization of phosphogypsum from Imbituba, Brazil.

    PubMed

    Borges, Renata Coura; Ribeiro, Fernando Carlos Araujo; Lauria, Dejanira da Costa; Bernedo, Alfredo Victor Bellido

    2013-12-01

    This research aims to characterize the content of natural occurring radionuclides in phosphogypsum stacks at Imbituba, Santa Catarina state, Brazil. (226)Ra, (228)Ra, (40)K, (238)U and (232)Th were determined in PG, soils and sediment samples by gamma spectrometry using the hyper pure germanium detector and neutron activation. The migration of radionuclides in the phosphogypsum profile did not show the same behavior for all sampling sites. The mean activity concentration of (226)Ra was 95 Bq kg(-1), which is far below the limit recommended by the U.S. Environmental Agency (USEPA) for its application in agriculture (370 Bq kg(-1)) and the Brazilian Commission of Nuclear Energy Resolution 113 that established a reference level of 1000 Bq kg(-1) of (226)Ra or (228)Ra for the use of PG in agriculture as well as building materials.

  19. Assessing Natural Radionuclide Migration in the Legacy Tailings of Uranium Production

    NASA Astrophysics Data System (ADS)

    Bondarenko, G.; Koliabina, I.; Marinich, O.

    2011-12-01

    The former Prydniprovsky Chemical Plant in Dniprodzerzhynsk, Ukraine, processed uranium ore from 1949 until 1991. Multiple tailing ponds containing solid residual waste products from the uranium leaching and processing of uranium were accumulated along the Dnieper River, including the largest, adjacent to the Dnieper Reservoir, containing over 12 million tons of tailings. Samples for this study were selected from a core recovered from the Dnieper tailing pit in 2009, and used to assess radionuclide migration from tailing ponds. Samples were selected from different depths of the tailing pit core, analyzed for total radionuclide concentrations [Marinich et al., 2009], and successively leached using distilled water, followed by 1N ammonium acetate solution, and finally by 1N HCl solution. Leaching times were ~24 h at 15.17 °C. 238U, 230Th and 226Ra leachate activities were measured by γ-spectrometry with a Ge(Li) detector. 210Pb activity was measured using a SEB-01 scintillation β-spectrometer. Errors depended on measuring method, radionuclide, activity and exposure time: 238U, 11.9%; 230Th, 10.9%; 226Ra, 9.3%; 210Pb ~30%. The average total 238U activity in the tailing profile was 4 Bq/g. The concentration of 238U in the water leachates increased with depth from 14.5% (7-7.5 m), to 43% (11-11.5 m). The concentration of 238U in the acid leachates behaved similarly, increasing from 5.5 % to 15.5% with depth. While the total 230Th activity in increased from 30 Bq/g (7-7.5 m) to 540 Bq/g (11-11.5 m), the 230Th concentration in ammonium acetate leachates decreased from ˜15% to ˜1%. The concentration of 226Ra in all leachates was <1%, indicating that, under conditions of the Dnieper tailing pit, 226Ra is essentially immobile. The concentration of 210Pb in the leachates was as high as 10%. In general, the magnitude of mobile activity from the Dnieper tailing pit core samples decreases in the order 238U>230Th≥210Pb> 226Ra. Secular radioactive equilibrium in the 238U

  20. Variation of uranium isotopic composition in soil within the JCO grounds from the 30 September 1999 criticality accident at JCO, Tokai-mura, Japan.

    PubMed

    Yamamoto, Masayoshi; Kawabata, Yoshiko; Murata, Yoshimasa; Komura, Kazuhisa

    2002-08-01

    Following the 30 September 1999 criticality accident at JCO, 29 surface and 3 core soil samples were collected inside and outside the JCO grounds to evaluate possible contamination by 235U-enriched uranium (18.8%) being handled at the time of the accident. Uranium (234U, 235U, and 238U) and thorium (228Th, 230Th, and 232Th) isotopes were determined by alpha-spectrometry and ICP-MS after radiochemical separation. Concentrations of 238U and 234U ranged from 11.3 to 63.5 and 11.6 to 360 mBq g(-1), respectively. Higher amounts of 238U and/or 234U were found in the vicinity of the uranium conversion building. The calculated 234U/235U activity ratios ranged from a 1.0 radioactive equilibrium value to an unusually high 5.7 value. Several of the soil samples showed considerably higher 235U/238U atomic ratios (1.06-4.37%) than 0.725% for natural uranium. Based on the assumption that measured U-series nuclides in soil samples taken from the JCO grounds were almost at radioactive equilibrium up to 230Th, excess uranium could be calculated for each sample. The results suggest that the excess uranium in the soils have lower 235U/238U atomic ratios (a few %) than the 18.8% enrichment of the precipitation tank uranium.

  1. A garage sale bargain: A leaking 2.2 GBq {sup 226}Ra source, Phase 1 - the incident

    SciTech Connect

    Freeman, B.; Andrews, M.; Hogan, A.

    1996-06-01

    In March 1995, a private citizen living in Bristol, Tennessee, went to a local garage sale and purchased a box containing old medical equipment and paraphernalia for $10.00. The man put the box in the trunk of his car where it remained for several weeks. He then took the box into his home where he examined all of the items, including a small wooden box with a metal sleeve. After significant effort, he managed to remove the inner box which bore the word {open_quotes}radium.{close_quotes} Unsure of what this meant, he called his son-in-law who understood that radium was a radioactive material and called the Tennessee Division of Radiological Health (TDRH). The TDRH investigation quickly located and isolated the source and determined that the contamination was spread throughout the man`s home and yard. Exposure rate readings as high as 160 mR h{sup -1} were found along with removable contamination as high as 3,000,000 dpm/100 cm{sup 2}. Over the next several days, the TDRH organized a voluntary effort for the medical evaluation of the man and his wife, the removal of the source, and the decontamination of the home, yard, car, etc. The two following papers will describe these aspects of this incident. On 26 May 1995, the remediation was completed, ending this unusual, but not unique, radiation incident.

  2. Ultrafast source-to-surface movement of melt at island arcs from 226Ra-230Th systematics.

    PubMed

    Turner, S; Evans, P; Hawkesworth, C

    2001-05-18

    Island arc lavas have radium-226 excesses that extend to higher values than those observed in mid-ocean ridge or ocean island basalts. The initial ratio of radium-226 to thorium-230 is largest in the most primitive lavas, which also have the highest barium/thorium ratios, and decreases with increasing magmatic differentiation. Therefore, the radium-226 excesses appear to have been introduced into the base of the mantle melting column by fluids released from the subducting plate. Preservation of this signal requires transport to the surface arguably in only a few hundreds of years and directly constrains the average melt velocity to the order of 1000 meters per year. Thus, melt segregation and channel formation can occur rapidly in the mantle.

  3. Measurement of {sup 222}Rn flux, {sup 222}Rn emanation and {sup 226}Ra concentration from injection well pipe scale

    SciTech Connect

    Rood, A.S.; Kendrick, D.T.

    1996-02-01

    The presence of Naturally Occurring Radioactive Material (NORM) has been recognized since the early 1930s in petroleum reservoirs and in oil and gas production and processing facilities. NORM was typically observed in barite scale that accumulated on the interior of oil production tubing and in storage tank and heater-treater separation sludge. Recent concern has been expressed over the health impacts from the uncontrolled release of NORM to the public. There are several potential exposure pathways to humans from oil-field NORM. Among these is inhalation of radon gas and its daughter products. For this exposure pathway to be of any significance, radon must first be released from the NORM matrix and diffuse in free air. The radon emanation fraction refers to the fraction of radon atoms produced by the decay of radium, that migrate from the bulk material as free gaseous atoms. The purpose of this investigation was to characterize the radon release rates from NORM-scale contaminated production tubing being stored above ground, characterize the radon emanation fraction of the bulk scale material when removed from the tubing, and characterize the radium concentrations of the scale. Accurate characterization of {sup 222}Rn emanation fractions from pipe scale may dictate the type of disposal options available for this waste. Characterization of radon release from stored pipes will assist in determining if controls are needed for workers or members of the public downwind from the source. Due to the sensitive nature of this data, the location of this facility is not disclosed.

  4. Q-value effects on the production of superheavy nuclei

    SciTech Connect

    Liu, Z. H.; Bao, Jing-Dong

    2006-11-15

    The formation of superheavy nucleus {sup 270}Hs via the 4n evaporation channel of fusion reactions {sup 26}Mg+{sup 248}Cm, {sup 30}Si+{sup 244}Pu, {sup 36}S+{sup 238}U, and {sup 48}Ca+{sup 226}Ra is studied using a two-parameter Smoluchowski equation. The evaporation residual cross sections of the reactions {sup 48}Ca+{sup 226}Ra and {sup 36}S+{sup 238}U are obviously enhanced because of their large negative Q values. The enhancement is due to the fact that the excitation energy corresponding to the maximum yield of the evaporation residue depends on the reaction Q value, and the maximum cross section sensitively depends on the increment of this excitation energy relative to the effective threshold energy of which the channel for fission after 4n emission opens.

  5. Mussels (Mytilus galloprovincialis) as a bio-indicator species in radioactivity monitoring of Eastern Adriatic coastal waters.

    PubMed

    Krmpotić, Matea; Rožmarić, Martina; Barišić, Delko

    2015-06-01

    Croatian Adriatic coastal waters are systematically monitored within the Mediterranean Mussel Watch Project using mussels (Mytilus galloprovincialis) as a bio-indicator species. The study includes determination of naturally occurring ((7)Be, (40)K, (232)Th, (226)Ra and (238)U), as well as anthropogenic (137)Cs radionuclides. Activity concentrations in dry weight of mussels' soft tissue along the Croatian Adriatic coast are presented, with spatial and seasonal variations given and discussed. Samples were collected in spring and autumn for the period between 2009 and 2013. Radionuclides were determined by gamma-ray spectrometry. Activity concentrations of (7)Be were the highest in spring periods, especially in the areas with significant fresh water discharges. Activity concentrations of (40)K did not vary significantly with season or location. (137)Cs activities were low, while (232)Th, (226)Ra and (238)U activities were mostly below the detection limit of performed gamma-spectrometric measurement.

  6. Variations in the uranium isotopic compositions of uranium ores from different types of uranium deposits

    NASA Astrophysics Data System (ADS)

    Uvarova, Yulia A.; Kyser, T. Kurt; Geagea, Majdi Lahd; Chipley, Don

    2014-12-01

    Variations in 238U/235U and 234U/238U ratios were measured in uranium minerals from a spectrum of uranium deposit types, as well as diagenetic phosphates in uranium-rich basins and peraluminous rhyolites and associated autunite mineralisation from Macusani Meseta, Peru. Mean δ238U values of uranium minerals relative to NBL CRM 112-A are 0.02‰ for metasomatic deposits, 0.16‰ for intrusive, 0.18‰ for calcrete, 0.18‰ for volcanic, 0.29‰ for quartz-pebble conglomerate, 0.29‰ for sandstone-hosted, 0.44‰ for unconformity-type, and 0.56‰ for vein, with a total range in δ238U values from -0.30‰ to 1.52‰. Uranium mineralisation associated with igneous systems, including low-temperature calcretes that are sourced from U-rich minerals in igneous systems, have low δ238U values of ca. 0.1‰, near those of their igneous sources, whereas uranium minerals in basin-hosted deposits have higher and more variable values. High-grade unconformity-related deposits have δ238U values around 0.2‰, whereas lower grade unconformity-type deposits in the Athabasca, Kombolgie and Otish basins have higher δ238U values. The δ234U values for most samples are around 0‰, in secular equilibrium, but some samples have δ234U values much lower or higher than 0‰ associated with addition or removal of 234U during the past 2.5 Ma. These δ238U and δ234U values suggest that there are at least two different mechanisms responsible for 238U/235U and 234U/238U variations. The 234U/238U disequilibria ratios indicate recent fluid interaction with the uranium minerals and preferential migration of 234U. Fractionation between 235U and 238U is a result of nuclear-field effects with enrichment of 238U in the reduced insoluble species (mostly UO2) and 235U in oxidised mobile species as uranyl ion, UO22+, and its complexes. Therefore, isotopic fractionation effects should be reflected in 238U/235U ratios in uranium ore minerals formed either by reduction of uranium to UO2 or chemical

  7. Influence of entrance channel on the production of hassium isotopes

    NASA Astrophysics Data System (ADS)

    Hong, Juhee; Adamian, G. G.; Antonenko, N. V.

    2015-07-01

    The production of hassium isotopes Hs-271266 in various reactions 22Ne+249Cf,Mg,2625+248Cm,30Si+244Pu,S,3634+238U,40Ar+232Th , and 48Ca+226Ra is studied within the dinuclear system model. The experimental excitation functions of the isotopes 266 -271Hs are well described and predictions are made for future experiments.

  8. The behavior of the uranium decay chain nuclides and thorium during the flank eruptions of Kilauea (Hawaii) between 1983 and 1985

    SciTech Connect

    Reinitz, I.M.; Turekian, K.K. )

    1991-12-01

    The concentrations of members of the {sup 238}U decay chain and {sup 232}Th have been determined for the lavas that erupted on the East Rift Zone of Kilauea Volcano, Hawaii (Puu Oo) between January 1983 and January 1985. There was a decrease during the first 180 days in the abundances of all nuclides, following the behavior of the incompatible elements. ({sup 230}Th/{sup 238}U) varies with ({sup 232}Th/{sup 238}U) yielding a batch process age for the source magma of 127,800 {plus minus} 28,500 (2{omega}) y, similar to East Pacific Rise basalts. No ({sup 226}Ra/{sup 230}Th) disequilibrium was evident at Puu Oo although Haleakala and Loihi show significant excesses of ({sup 226}Ra) over ({sup 230}Th). The initial ({sup 210}Pb) excess relative to ({sup 226}Ra) implies strong incompatibility of {sup 210}Pb probably with the help of chloride complexing, and the deficiency in later episodes indicates volatilization from the melt mediated by the formation of volatile chloride compounds.

  9. Radon in soil gas in Kosovo.

    PubMed

    Kikaj, Dafina; Jeran, Zvonka; Bahtijari, Meleq; Stegnar, Peter

    2016-11-01

    An assessment of the radiological situation due to exposure to radon and gamma emitting radionuclides was conducted in southern Kosovo. This study deals with sources of radon in soil gas. A long-term study of radon concentrations in the soil gas was carried out using the SSNTDs (CR-39) at 21 different locations in the Sharr-Korabi zone. The detectors were exposed for an extended period of time, including at least three seasonal periods in a year and the sampling locations were chosen with respect to lithology. In order to determine the concentration of the natural radioactive elements (238)U and (226)Ra, as a precursor of (222)Rn, soil samples were collected from each measuring point from a depth of 0.8 m, and measured by gamma spectrometry. The levels (Bq kg(-1)) of naturally occurring radionuclides and levels (kBq m(-3)) of radon in soil gas obtained at a depth 0.8 m of soil were: 21-53 for (226)Ra, 22-160 for (238)U and 0.295-32 for (222)Rn. With respect to lithology, the highest value for (238)U and (226)Ra were found in limestone and the highest value for (222)Rn was found in metamorphic rocks. In addition, the results showed seasonal variations of the measured soil gas radon concentrations with maximum concentration in the spring months.

  10. Evaluation of radiation hazard potential of TENORM waste from oil and natural gas production.

    PubMed

    Hilal, M A; Attallah, M F; Mohamed, Gehan Y; Fayez-Hassan, M

    2014-10-01

    In this study, a potential radiation hazard from TENORM sludge wastes generated during exploration and extraction processes of oil and gas was evaluated. The activity concentration of natural radionuclides (238)U, (226)Ra and (232)Th were determined in TENORM sludge waste. It was found that sludge waste from oil and gas industry is one of the major sources of (226)Ra in the environment. Therefore, some preliminary chemical treatment of sludge waste using Triton X-100 was also investigated to reduce the radioactivity content as well as the risk of radiation hazard from TENORM wastes. The activity concentrations of (226)Ra and (228)Ra in petroleum sludge materials before and after chemical treatment were measured using gamma-ray spectrometry. The average values of the activity concentrations of (226)Ra and (228)Ra measured in the original samples were found as 8908 Bq kg(-1) and 933 Bq kg(-1), respectively. After chemical treatment of TENORM samples, the average values of the activity concentrations of (226)Ra and (228)Ra measured in the samples were found as 7835 Bq kg(-1) and 574 Bq kg(-1), respectively. Activity concentration index, internal index, absorbed gamma dose rate and the corresponding effective dose rate were estimated for untreated and treated samples.

  11. Direct uranium isotope ratio analysis of single micrometer-sized glass particles

    PubMed Central

    Kappel, Stefanie; Boulyga, Sergei F.; Prohaska, Thomas

    2012-01-01

    We present the application of nanosecond laser ablation (LA) coupled to a ‘Nu Plasma HR’ multi collector inductively coupled plasma mass spectrometer (MC-ICP-MS) for the direct analysis of U isotope ratios in single, 10–20 μm-sized, U-doped glass particles. Method development included studies with respect to (1) external correction of the measured U isotope ratios in glass particles, (2) the applied laser ablation carrier gas (i.e. Ar versus He) and (3) the accurate determination of lower abundant 236U/238U isotope ratios (i.e. 10−5). In addition, a data processing procedure was developed for evaluation of transient signals, which is of potential use for routine application of the developed method. We demonstrate that the developed method is reliable and well suited for determining U isotope ratios of individual particles. Analyses of twenty-eight S1 glass particles, measured under optimized conditions, yielded average biases of less than 0.6% from the certified values for 234U/238U and 235U/238U ratios. Experimental results obtained for 236U/238U isotope ratios deviated by less than −2.5% from the certified values. Expanded relative total combined standard uncertainties Uc (k = 2) of 2.6%, 1.4% and 5.8% were calculated for 234U/238U, 235U/238U and 236U/238U, respectively. PMID:22595724

  12. Radioactivity in three species of eastern Mediterranean jellyfish.

    PubMed

    Mamish, S; Al-Masri, M S; Durgham, H

    2015-11-01

    Activity concentrations of (137)Cs, (40)K, (210)Po, (210)Pb, (234)U and (238)U were determined in umbrella and oral arms of three widely distributed jellyfish species; namely Rhopilema nomadica Galil, 1990, Aurelia aurita Linne, 1758 and Aequorea forskalea Péron & Lesueur, 1810 collected from February 2011 to January 2012 in four sampling locations along the Syrian coast (Eastern Mediterranean Sea). The results have shown significant variations in radionuclides activity concentrations amongst the species. The average activity concentrations of (40)K, (210)Po, (210)Pb, (234)U and (238)U in the umbrella of R. nomadica species were higher than the average activity concentrations in the umbrella of A. aurita species by about 3.2, 1.4, 1.8, 3.2 and 3.2 folds, and A. forskalea species by about 45.5, 15.4, 19, 7.4 and 7.6 folds, respectively. The average activity concentrations of (40)K, (210)Po, (210)Pb, (234)U and (238)U in oral arms of R. nomadica species were higher than the average activity concentrations in oral arms of A. aurita species by about 3.8, 1.7, 1.9, 2.8 and 2.9 folds, respectively. (137)Cs activity concentrations were below the detection limit in all measured samples. In addition, activity concentrations of (137)Cs, (40)K, (210)Po, (210)Pb, (234)U and (238)U were also determined in 44 surface seawater samples and the activity concentrations ranged between 10.6 and 11.9 Bq l(-1) for (40)K, 1.1 and 1.4 mBq l(-1) for (210)Po, 0.5 and 0.7 mBq l(-1) for (210)Pb, 40.8 and 44.5 mBq l(-1) for (234)U, and 36.9 and 38.4 mBq l(-1) for (238)U, while (137)Cs activity concentrations were below the detection limit in all measured samples. Moreover, the umbrella and oral arms readily accumulated (40)K, (210)Po, (210)Pb, (234)U and (238)U above ambient seawater levels in the sequence of (210)Po > (210)Pb > (4) K > (234)U and (238)U. Concentration ratio (CR) values were relatively high for (210)Po and (210)Pb and reached 10(3) and 10(2), respectively for the jellyfish R

  13. Calibration of fossil scleraxonian Southern Ocean deep-sea corals for U-series dating

    NASA Astrophysics Data System (ADS)

    Gutjahr, M.; Vance, D.; Hoffmann, D.; Hillenbrand, C.; Kuhn, G.

    2008-12-01

    The deep Southern Ocean has been pinpointed as candidate reservoir capable of storing the additional respired carbon that was drawn from the atmosphere during the Last Glacial Maximum compared with the present-day. In this context the determination of deep ocean ventilation ages is a commonly applied tool, potentially identifying radiocarbon depletion in glacial deep water and enhanced ocean stratification. In order to derive deep-sea ventilation ages most studies to date have used either radiocarbon age differences between paired planktic and benthic foraminifera samples or coupled U-Th and radiocarbon dates obtained from aragonitic deep-sea corals. Results from both these approaches are, however, as yet very scarce for the Southern Ocean. We present calendar ages for a set of deep-sea scleraxonian corals from the Marie Byrd Seamounts in the Amundsen Sea sector of the Southern Ocean (~123°W, ~69°S, 2500 m to 1430 m water depth) employing the 230Th/U-dating method. The aim of our study is to evaluate whether these calcitic octocorals can be used for ventilation age determinations. Our corals have significantly lower uranium concentrations than aragonitic deep-sea corals, ranging from 80 to 250 ng/g. Most corals of Holocene age reproduced the present-day seawater 234U/238U. Pre-Holocene corals, however, show a systematic enrichment of 234U, leading to slightly elevated deglacial initial 234U/238U and significantly higher 234U/238U for ~MIS5 sub-samples. These corals also appear to grow very slowly, on the order of only few μm/year, making it essential to sample as little coral material as possible for combined 230Th/U- and radiocarbon dating purposes. One coral, sampled at high-resolution in various sections returned ages that scatter around 10 ka BP and the early deglaciation, though several significantly older ages were obtained as well. The present-day (234U/238U) ACT in different sections of this coral is very homogenous (1.155 ± 0.003) and more or less

  14. Determination of U isotope ratios in sediments using ICP-QMS after sample cleanup with anion-exchange and extraction chromatography.

    PubMed

    Zheng, Jian; Yamada, Masatoshi

    2006-01-15

    The determination of uranium is important for environmental radioactivity monitoring, which investigates the releases of uranium from nuclear facilities and of naturally occurring radioactive materials by the coal, oil, natural gas, mineral, ore refining and phosphate fertilizer industries, and it is also important for studies on the biogeochemical behavior of uranium in the environment. In this paper, we describe a quadrupole ICP-MS (ICP-QMS)-based analytical procedure for the accurate determination of U isotope ratios ((235)U/(238)U atom ratio and (234)U/(238)U activity ratio) in sediment samples. A two-stage sample cleanup using anion-exchange and TEVA extraction chromatography was employed in order to obtain accurate and precise (234)U/(238)U activity ratios. The factors that affect the accuracy and precision of U isotope ratio analysis, such as detector dead time, abundance sensitivity, dwell time and mass bias were carefully evaluated and corrected. With natural U, a precision lower than 0.5% R.S.D. for (235)U/(238)U atom ratio and lower than 2.0% R.S.D. for (234)U/(238)U activity ratio was obtained with less than 90 ng uranium. The developed analytical method was validated using an ocean sediment reference material and applied to an investigation into the uranium isotopic compositions in a sediment core in a brackish lake in the vicinity of U-related nuclear facilities in Japan.

  15. URANIUM-SERIES DISEQUILIBRIUM IN TUFF AND GRANITE:HYDROGEOLOGICAL IMPLICATIONS

    SciTech Connect

    M. Gasscoyne; N.H. Miller

    2000-10-27

    radionuclide involved. Depending on the analytical precision obtained, the observation of a {sup 234}U/{sup 238}U activity ratio that is less than or greater than 1.000 clearly shows that an isotope of uranium has migrated within the rock in the last 1-2 million years. Other daughter/parent activity ratios can be used to detect radionuclide migration over shorter time-scales, such as {sup 230}Th/{sup 234}U (300,000 years) and {sup 226}Ra/{sup 230}Th (8,000 years). Uranium-series disequilibrium is, therefore, a useful technique for application to site evaluation for nuclear fuel waste disposal because it can be used to: (1) show that so-called ''intact rock'' is indeed intact (i.e. radionuclides are in secular equilibrium and are immobile), (2) determine the principal flow regimes in a rock mass by analysis of rock matrix, fracture material, etc., (3) estimate the time period of recent radionuclide migration in the rock, and (4) proxy as a natural analogue for the potential mobility of uranium at the site. Several examples of these applications have been reported. This paper describes the use of uranium-series disequilibrium in the comparison of two North American sites: the water-saturated Lac du Bonnet granite batholith on the Canadian Shield and the unsaturated tuffs from the Exploratory Studies Facility (ESF) and Cross-Drift Tunnels at Yucca Mountain, Nevada. In particular, the fact that unfractured rock should be at secular equilibrium is applied to both sites to determine if the rock matrix is a significant flow path for groundwater.

  16. Uranium-series constraints on radionu