The measurement of gamma-emitting radionuclides in beach sand cores of coastal regions of Ramsar,Iran using HPGe detectors

Radionuclides which present in different beach sands are sources of external exposure that contribute to the total radiation exposure of human. ²²⁶Ra, ²³⁵U, ²³²Th, ⁴⁰K and ¹³⁷Cs analysis has been carried out in sand samples collected at six depth levels, from eight locations of the northern coast of Iran, Ramsar, using high-resolution gamma-ray spectroscopy. The average Specific activities of natural radionuclides viz., ²²⁶Ra, ²³⁵U, ²³²Th, ⁴⁰K and ¹³⁷Cs, in the 0–36 cm depth sand were found as: 19.2 ± 0.04, 2.67 ± 0.17, 17.9 ± 0.06, 337.5 ± 0.61 and 3.35 ± 0.12 Bq kg⁻¹, respectively. The effects of organic matter content and pH value of sand samples on the natural radionuclide levels were also investigated. Finally, the measured radionuclide concentrations in the Ramsar beach were compared with the world average values, as reported by UNSCEAR (2000). None of the studied beaches were considered as a radiological risk.     

Distribution of radioactive pollution of 238U, 232Th, 40K and 137Cs in northwestern coasts of Persian Gulf, Iran

A reconnaissance study has been made of the distribution of 238U, 232Th, 40K and 137Cs and geochemical features in soils and sediments samples at various locations in the northwestern coast of Persian Gulf. Activity concentration levels due to radionuclides were measured in 30 soil and sediment samples collected from this region. From the measured spectra, activity concentrations were determined for 40K (range from 146 to 500 Bq kg(-1)), 137Cs (from 5 to 20 Bq kg(-1)), 238U (from 21 to 65 Bq kg(-1)) and 232Th (from 15 to 45 Bq kg(-1)) with lowest limit detection (LLD) of 68, 3.2, 4.3 and 4.3 Bq kg(-1), respectively. The dose rate from ambient air at the soil ranges was between 19 and 58 nGy h(-1) with an average of 37.41+/-9.66 nGy h(-1).     

(235)U, (238)U, (232)Th, (40)K and (137)Cs activity concentrations in marine sediments along the northern coast of Oman Sea using high-resolution gamma-ray spectrometry

The natural radioactivity levels in sediment samples of the northern coast of Oman Sea, covering the coastal strip from Hormoz canyon to Goatr seaport, as the first time has been determined. The results of measurements will serve as background reference level for Oman Sea coastlines. Sediments from 36 coastal and near shore locations were collected for analysis. Analysis on the collected samples were carried out to determine (235)U, (238)U, (232)Th, (40)K and (137)Cs using two high purity germanium detectors with 38.5% and 55% relative efficiencies. The concentration of (235)U, (238)U, (232)Th, (40)K and (137)Cs in sediment samples ranged between 1.01 and 2.87Bq/kg, 11.83 and 22.68Bq/kg, 10.7 and 25.02Bq/kg, 222.89 and 535.07Bq/kg and 0.14 and 2.8Bq/kg, respectively. The radium equivalent activity was well below the defined limit of 370Bq/kg. The external hazard indices were found to be less than 1, indicating a low dose.     

Altitude-dependent distribution of ~(137)Cs in the environment:a case study of Aragats massif,Armenia

This paper considers the distribution of technogenic 137Cs and naturally occurring radionuclides:238 U,232 Th and40 R concentrations in soils and 137Cs in atmospheric dry depositions by altitudinal belts of the Aragats mountain massif,Republic of Armenia.Undisturbed soil samples were collected at altitudes from 1000 to 3200 m.For the determination of geochemical variability,two soil sampling campaigns were undertaken.Atmospheric dry depositions were sampled from five stations at1100-3200 m collected onto organic fiber filters between June and December 2016.137Cs activity was measured using a high-purity Germanium detector coupled to a multichannel analyzer(Canberra).Results indicated that specific activity of 137Cs in soils at 1000 m is495-528 Bq m^-2,andat3200 mis10,500-11,470 Bq m^-2.No correlation observed for 137Cs versus naturally occurring radionuclides,which varies in distribution by altitude.Specific activities of 137Cs in dry atmospheric depositions varies from 1.06 at 846 m to2.37 Bq m^-2 per quarter at 3200 m and increases as the altitude increases.Activities of 137Cs in soil and dry atmospheric deposition correlated significantly,and 137Cs activity in soils and atmospheric dry depositions decrease as the absolute altitude decreases.The 50-year effective dose from exposure to 137Cs fallout varies with altitude from 0.007 to 1.42 m Sv.     

Distribution of local Cs anomalies on the seafloor near the Fukushima Dai-ichi Nuclear Power Plant

An estimated 3.5 ± 0.7 × 10¹⁵ Bq of ¹³⁷Cs is thought to have been discharged into the ocean following the melt down at Fukushima Dai-ichi Nuclear Power Plant (F1NPP). While efforts have been made to monitor seafloor radiation levels, the sampling techniques used cannot capture the continuous distribution of radionuclides. In this work, we apply in situ measurement techniques using a towed gamma ray spectrometer to map the continuous distribution of ¹³⁷Cs on the seafloor within 20 km of the F1NPP. The results reveal the existence of local ¹³⁷Cs anomalies, with levels of ¹³⁷Cs an order of magnitude higher than the surrounding seafloors. The sizes of the anomalies mapped in this work range from a few meters to a few hundreds of meters in length, and it is demonstrated that the distribution of these anomalies is strongly influenced by meter scale features of the terrain.     

Levels of Po and Pb in mussel and sediments in Candarlı Gulf and the related dose assessment to the coastal population

²¹⁰Po and ²¹⁰Pb in mussel (Mytilus galloprovincialis) and sediment samples collected at Candarl? Gulf during the period of 2010–2012 are presented and discussed. The activity concentrations of ²¹⁰Po and ²¹⁰Pb were measured by means of alpha spectrometry. Activity concentrations of ²¹⁰Po and ²¹⁰Pb in mussels are in the ranged of 332 ± 17–776 ± 23 Bq kg⁻¹ dw and 14 ± 1–40 ± 5 Bq kg⁻¹ dw, for sediments the ranges for 52 ± 5–109 ± 8 Bq kg⁻¹ dw and 38 ± 5–92 ± 9 Bq kg⁻¹ dw, respectively. The estimated consequent annual effective ingestion dose due to ²¹⁰Po and ²¹⁰Pb from mussel consumption in Candarl? Gulf coastal region were calculated. The highest dose due to ²¹⁰Po and ²¹⁰Po were calculated to be 4232 ± 126 μSv and 126 ± 16 μSv, respectively.     

Modelling temporal trends of 137Cs and 99Tc concentrations in Fucus vesiculosus from the eastern Irish coastline

Time series of ¹³⁷Cs and ⁹⁹Tc activity concentrations in the brown seaweed Fucus vesiculosus and seawater, gathered at three locations on the eastern Irish coastline during the period 1988-2008, have been modelled using a novel approach incorporating a variable uptake rate in the seaweed. Seasonal variations in the time series, identified using spectral analysis, were incorporated into the model which was used to determine transfer kinetic parameters and to predict ¹³⁷Cs and ⁹⁹Tc concentrations in seaweed, as influenced by levels in ambient seawater. An optimisation method combining evolutionary and grid search minimisation techniques was adopted to determine the best values for the model parameters, from which concentration factors (CF) and biological half-lives (tb_1/2) for ¹³⁷Cs and ⁹⁹Tc in F. vesiculosus were calculated. CF values of 170-179 and 1.1 × 105 l kg⁻¹ (dry weight) were obtained for ¹³⁷Cs and ⁹⁹Tc, respectively, while the corresponding tb_1/2 values were 39-47 and 32 days, respectively.     

Bioconcentration of triclosan and methyl-triclosan in marine mussels (Mytilus galloprovincialis) under laboratory conditions and in metropolitan waters of Gulf St Vincent,South Australia

The anti-microbial agent triclosan (TCS), and its derivative methyl-triclosan (Me-TCS), are discharged with treated effluents from wastewater treatment plants to receiving environments. We investigated the bioconcentration of TCS and Me-TCS in mussels (Mytilus galloprovincialis) exposed to TCS (100 ng L⁻¹) for 30 days in seawater aquaria (19 ± 2 °C) with fresh phytoplankton as a food source. Bioconcentration increased with time reaching a steady-state around 24–30 days. The bioconcentration factor (log BCF) for TCS were 2.81 L kg⁻¹ (dry weight) and 4.13 L kg⁻¹, when lipid normalised concentrations were used. Mussels were also deployed in cages at four marine locations receiving effluents from WWTPs. The mean (±SD) TCS and Me-TCS concentrations for mussels from these sites were 9.87 (±1.34) and 6.99 (±2.44) μg kg⁻¹. The study showed that mussels can be a useful tool for monitoring pollution of TCS and Me-TCS in marine and estuarine environments.     

Assessment of health safety from ingestion of natural radionuclides in seafoods from a tropical coast, India

The activities of ²¹⁰Po and ²¹⁰Pb were determined in commonly consumed seafoods to evaluate the internal exposure and risk to humans residing Kudankulam coast where a mega nuclear power plant is under construction. The concentration of ²¹⁰Po in seafoods ranged from 1.2 ± 0.7 to 248 ± 8.1 Bq kg⁻¹. Meanwhile, ²¹⁰Pb ranged between 1.1 ± 0.05 and 14.8 ± 1.6 Bq kg⁻¹. The committed effective dose (CED) due to ²¹⁰Po and ²¹⁰Pb varied from 11.04 to 515.6 and 3.93 to 23.5 μSv yr⁻¹, respectively. The lifetime cancer risk for the public due to ²¹⁰Po was in the range of 3.47 × 10⁻⁵-1.62 × 10⁻³ and it was 4.03 × 10⁻⁵-1.96 × 10⁻⁴ due to ²¹⁰Pb. The activity intake, effective dose and cancer risk was found lesser than international guidelines and the seafood intake was considered to be safe for human consumption.     

Lead in blood and eggs of the sea turtle, Lepidochelys olivacea, from the Eastern Pacific: Concentration, isotopic composition and maternal transfer

Concentrations of lead were assessed in the sea turtle, Lepidochelys olivacea, from a nesting colony of the Eastern Pacific. Twenty-five female turtles were sampled and a total of 250 eggs were collected during the “arribada” event of the 2005-2006 season. Considering the nesting season, the maternal transfer of lead (Pb) via egg-laying, in terms of metal burden in whole body, was 0.5%. Pb concentrations (in dry weight) in blood (0.95 ± 0.18 μg g⁻¹) and egg samples (yolk, 0.80 ± 0.10 μg g⁻¹; albumen, 1.08 ± 0.20 μg g⁻¹; eggshell, 1.05 ± 0.20 μg g⁻¹) were comparable or even lower than those found in other sea turtles. The isotope ratios (²⁰⁶Pb/²⁰⁷Pb and ²⁰⁶Pb/²⁰⁸Pb) in blood (1.183 ± 0.0006 and 2.452 ± 0.0006, respectively) were comparable to that of natural Pb-bearing bedrock in Mexico (1.188 ± 0.005 and 2.455 ± 0.008, respectively). According to international norms of Pb, the health of this population and its habitats is acceptable for Pb and corresponds to basic levels of a nearly pristine environment.     

U-series dating of Lake Nyos maar basalts,Cameroon (West Africa): Implications for potential hazards on the Lake Nyos dam

From previously published ¹⁴C and K–Ar data, the age of formation of Lake Nyos maar in Cameroon is still in dispute. Lake Nyos exploded in 1986, releasing CO₂ that killed 1750 people and over 3000 cattle. Here we report results of the first measurements of major elements, trace elements and U-series disequilibria in ten basanites/trachy-basalts and two olivine tholeiites from Lake Nyos. It is the first time tholeiites are described in Lake Nyos. But for the tholeiites which are in ²³⁸U–²³⁰Th equilibrium, all the other samples possess ²³⁸U–²³⁰Th disequilibrium with 15 to 28% enrichment of ²³⁰Th over ²³⁸U. The (²²⁶Ra/²³⁰Th) activity ratios of these samples indicate small (2 to 4%) but significant ²²⁶Ra excesses. U–Th systematics and evidence from oxygen isotopes of the basalts and Lake Nyos granitic quartz separates show that the U-series disequilibria in these samples are source-based and not due to crustal contamination or post-eruptive alteration. Enrichment of ²³⁰Th is strong prima facie evidence that Lake Nyos is younger than 350 ka. The ²³⁰Th–²²⁶Ra age of Nyos samples calculated with the (²²⁶Ra/²³⁰Th) ratio for zero-age Mt. Cameroon samples is 3.7 ± 0.5 ka, although this is a lower limit as the actual age is estimated to be older than 5 ka, based on the measured mean ²³⁰Th/²³⁸U activity ratio. The general stability of the Lake Nyos pyroclastic dam is a cause for concern, but judging from its ²³⁰Th–²²⁶Ra formation age, we do not think that in the absence of a big rock fall or landslide into the lake, a big earthquake or volcanic eruption close to the lake, collapse of the dam from erosion alone is as imminent and alarming as has been suggested.     

Multi-method approach to dating glass: The case of Basiluzzo Islet (Aeolian archipelago,Italy)

A rhyolitic lava flow from Basiluzzo islet (Aeolian Islands), has been analysed with the Fission tracks (FT) and ⁴⁰Ar–³⁹Ar methods on glass, and with the U/Th method on whole rock to constrain its age and to compare the behaviour of different dating methodologies on glass samples late Quaternary in age. Laser ⁴⁰Ar–³⁹Ar total fusion analyses were performed on populations of grains. Due to the low yields of radiogenic ⁴⁰Ar the age data are characterised by very high errors. The weighted average of the ages of the whole population is 55.7 ± 8.7 ka (MSWD = 0.7). The isochron age calculated on all points is 40.6 ± 11.4 ka (MSWD = 0.6), with an initial ⁴⁰Ar/³⁶Ar ratio of 297.8 ± 1.8; the isochron is characterised by very little spread among points. The procedure named ‘point-counting technique’ was adopted in FT dating. Spontaneous track mean size resulted reduced by around 20% compared to induced tracks, which indicates that the determined FT age, 28.6 ± 3.6 ka, is a reduced age, due to a certain amount of track annealing. For this reason the plateau technique for correcting thermally lowered ages was applied. We determined a plateau age (commonly assumed as a reliable estimate of the glass formation age) of 43.4 ± 7.1 ka. Four sub-samples of whole rock from Basiluzzo lava flow have been analysed using U/Th isochron method. The ²³⁸U/²³²Th and ²³⁰Th/²³²Th activity ratios of sub-samples have been determined by alpha counting and plotted on an isochron diagram. The resulting age is 46 ± 8 ka and the ²³⁴U/²³⁸U activity ratios are always close to one, demonstrating that no significant processes of alteration have occurred. The relatively high error associated with the age is due to a low fractionation of U/Th ratio in the analysed whole rocks. The ages obtained with different methods, 43.4 ± 7.1 ka (FT plateau age), 40.6 ± 11.4 ka (⁴⁰Ar–³⁹Ar isochron age of all grains), and 46 ± 8 ka (U/Th isochron) agree at the 1σ level, excluding a Holocene age for this sample. This could be valuable information for the Department of Civil Protection because it seems to mitigate the potential risk for present volcanic activity in the area. All ages are affected by very high analytical errors, which are due to the characteristics of the material analysed. Young ages result in low tracks numbers (FT dating) and barely detectable amounts of radiogenic ⁴⁰Ar in the presence of high atmospheric contamination (⁴⁰Ar–³⁹Ar dating). Stratigraphic successions without strict chronologic constraints might however benefit even from age data with low precision.     

The application of caesium‐137 measurements to investigate floodplain deposition in a large semi‐arid catchment in Queensland,Australia: a low‐fallout environment

Floodplains comprise geomorphologically important sources and sinks for sediments and associated pollutants, yet the sedimentology of large dryland floodplains is not well understood. Processes occurring on such floodplains are often difficult to observe, and techniques used to investigate smaller perennial floodplains are often not practical in these environments. This study assesses the utility of ¹³⁷Cs inventory and depth‐profile techniques for determining relative amounts of floodplain sedimentation in the Fitzroy River, northeastern Australia; a 143 000 km² semi‐arid river system. Caesium‐137 inventories were calculated for floodplain and reference location bulk soil cores collected from four sites. Depth profiles of ¹³⁷Cs concentration from each floodplain site and a reference location were recorded. The areal density of ¹³⁷Cs at reference locations ranged from 13 to 978 Bq m^–2 (0–1367 Bq m^–2 at the 95% confidence interval), and the mean value ± 2 (standard error of the mean) was 436 ± 264 Bq m^–2, similar to published data from other Southern Hemisphere locations. Floodplain inventories ranged from 68 to 1142 Bq m^–2 (0–1692 Bq m^–2 at the 95% confidence interval), essentially falling within the range of reference inventory values, thus preventing calculation of erosion or deposition. Depth‐profiles of ¹³⁷Cs concentration indicate erosion at one site and over 66 cm of deposition at another since 1954. Analysis of ^239+240Pu concentrations in a depositional core substantiated the interpretation made from ¹³⁷Cs data, and depict a more tightly constrained peak in concentration. Average annual deposition rates range from 0 to 15 mm. The similarity between floodplain and reference bulk inventories does not necessarily indicate a lack of erosion or deposition, due to low ¹³⁷Cs fallout in the region and associated high measurement uncertainties, and a likely influence of gully and bank eroded sediments with no or limited adsorbed ¹³⁷Cs. In this low‐fallout environment, detailed depth‐profile data are necessary for investigating sedimentation using ¹³⁷Cs. Copyright © 2009 John Wiley & Sons, Ltd.     

The uranium and thorium decay series nuclides in Mt. St. Helens effusives

The concentrations of the radionuclides²³⁸U,²³⁰Th,²²⁶Ra,²¹⁰Pb,²¹⁰Po,²³²Th,²²⁸Ra and²²⁸Th and the abundances of major elements were determined in samples from all major eruptions of Mt. St. Helens from May 18, 1980 through June 21, 1981. During this time the effusives changed from plagioclase-phyric dacite to a more andesitic composition but the concentrations of U and Th series nuclides were measurably invariant. The average²³²Th/²³⁸U weight ratio in the rocks is 2.4 and the²³⁰Th/²³²Th activity ratio equals the²³⁸U/²³²Th activity ratio indicating no fractionation of U from Th during magma genesis.²²⁶Ra activity is in excess (～40% on average) of its parent²³⁰Th whereas²²⁸Ra is in radioactive equilibrium with its parent²³²Th, constraining the time of magma formation between 30 and 10⁴ years prior to eruption. The²¹⁰Pb/²²⁶Ra activity ratios in the samples average 1.0, with a 20% scatter on either side, but allowing for volatile²¹⁰Pb loss at time of eruption excess²¹⁰Pb over²²⁶Ra is inferred, indicating that the time of magma formation was within the last 150 years.²¹⁰Po was virtually absent in the samples immediately after eruption, indicating its total loss by volatilization during eruption. The quantity of²¹⁰Po volatilized during the May 18, 1980 event is estimated to be in the range of 300 Ci from the effusives and as much as 5000 Ci total including losses from heated slide material. The²²²Rn activity volatilized should have been comparable to the²¹⁰Po activity released.     

Natural radioactivity assessment of surface sediments in the Yangtze Estuary

The activities of the natural radionuclides (²³⁸U, ²³²Th, ²²⁶Ra and ⁴⁰K) of the surface sediments in the Yangtze Estuary were determined and used to evaluate radiation hazards in the study area. The of activities of ²³⁸U, ²³²Th, ²²⁶Ra and ⁴⁰K ranges from 14.1 to 62.3, 26.1 to 71.9, 13.7 to 52.3, and 392 to 898 Bq kg^? 1, respectively, which were comparable to values of other regions in China. The activities of ²³²Th, ⁴⁰K and ²²⁶Ra were clearly different from the global recommended values. The radium equivalent activity was less than the recommended limit of 370 Bq kg^? 1; therefore, the sediment in this area can be safely used for reclamation. The external hazard index values were less than one. The average absorbed gamma dose rate and annual effective dose equivalent values were slightly greater than the world average value. ²²⁶Ra/²³⁸U and ²³²Th/²³⁸U ratios could potentially be applied for tracing sediment source.     

Organohalogen contaminants and trace metals in North-East Atlantic porbeagle shark (Lamna nasus)

The North-East Atlantic porbeagle (Lamna nasus) population has declined dramatically over the last few decades and is currently classified as ‘Critically Endangered’. As long-lived, apex predators, they may be vulnerable to bioaccumulation of contaminants. In this study organohalogen compounds and trace elements were analysed in 12 specimens caught as incidental bycatch in commercial gillnet fisheries in the Celtic Sea in 2011. Levels of organohalogen contaminants were low or undetectable (summed CB and BDE concentrations 0.04–0.85 mg kg⁻¹ wet weight). A notably high Cd concentration (7.2 mg kg⁻¹ wet weight) was observed in one mature male, whereas the range observed in the other samples was much lower (0.04–0.26 mg kg⁻¹ wet weight). Hg and Pb concentrations were detected only in single animals, at 0.34 and 0.08 mg kg⁻¹ wet weight, respectively. These contaminant levels were low in comparison to other published studies for shark species.     

Uranium and thorium isotopes in the rivers of the Amazonian basin: hydrology and weathering processes

Two expeditions (October 1989 and May 1992) were carried out to two points of the main Amazon River channel and four tributaries. The Solimões and Madeira rivers, taking their origin in the Andes, are whitewater rivers. The Negro River is a typical acid, blackwater river. The Trombetas River flows through bauxite‐rich areas, and is characterized by low concentrations of dissolved humic substances. The ²³⁸U, ²³⁴U, ²³²Th and ²³⁰Th activities were recorded from dissolved, suspended particulate phases and river bank sediments. The latter were analysed for their ²²⁶Ra, ²²⁸Ra and ²¹⁰Pb contents, and also subjected to leaching with 0·2 M hydroxylamine–hydrochloride solution to determine the concentrations of radionuclides bound to amorphous Fe hydroxides and Mn oxides and hydroxides. The dissolved U average concentration in the Amazon system is ten times lower than the mean world river concentration. The uranium concentration observed at Óbidos in the lower Amazon (0·095 µg L^?1), where the U content in the river bank sediments and suspended matter is lowest, suggests U release from the solid phase during river transport. About 485 t of U are transported annually to the Amazon delta area in dissolved form, and 1943 t bound to suspended particulate matter. Total U and Th concentrations in the river bank sediments ranged from 1·59 to 7·14 µg g^?1 and from 6·74 to 32 µg g^?1, respectively. The highest concentrations were observed in the Trombetas River. The proportion extracted by means of the hydroxylamine solution (HL) was relatively high for U in the Trombetas river bank sediment (31%) and for Th in the Solimões sediment (30%). According to the alpha recoil effects, the ²³⁴U/²³⁸U activity ratios of the Andean river waters and downstream Amazon water (Óbidos) were >1, but were <1 in the Negro River (at Manaus). The activity ratios of dissolved U correlate with pH and also with the U activity ratios in the river bank sediment hydroxylamine extracts. As expected, the ²³⁴U/²³⁸U activity ratios in river bank sediments were <1 in the Andean rivers and in the downstream Amazon, but they were >1 in the Trombetas and Negro rivers. Such ratios probably result from the binding of dissolved uranium to solid sediment. The ²²⁸Th/²³²Th ratios of river bank sediments were close to unity (except for the Negro River, where it is lower), suggesting no significant Th exchanges between the river water and the sediment. The ²²⁶Ra/²³²Th activity ratios were <1, and the ²²⁶Ra/²²⁸Ra activity ratios generally were significantly higher than the activity ratios of their respective parents. This perhaps is the result of easier leaching of the ²²⁶Ra parent, ²³⁰Th, from solid material (owing to the alpha recoil effect) than of the ²²⁸Ra parent. Uranium and thorium isotopes were used as tools to evaluate the chemical weathering rate of rocks in the Amazon system, which was estimated to be 2·7 cm 1000 year^?1 s^?1. Copyright © 2002 John Wiley & Sons, Ltd.     

Rapid uranium-series age screening of carbonates by laser ablation mass spectrometry

Uranium-series dating is a critical tool in quaternary geochronology, including paleoclimate work, archaeology and geomorphology. Laser ablation (LA) methods are not as precise as most isotope dilution methods, but can be used to generate calendar ages rapidly, expanding the range of dating tools that can be applied to late Pleistocene carbonates. Here, existing LA methods are revisited for corals (cold- and warm-water) and speleothems spanning the last 343 thousand years (ka). Measurement of the required isotopes (²³⁸U, ²³⁴U, ²³⁰Th and ²³²Th) is achieved by coupling a laser system to a multi-collector inductively-coupled-plasma mass spectrometer (MC-ICPMS) using a combination of a single central ion counter and an array of Faraday cups. Each sample analysis lasts for ∼4.3 min, and fifty samples can be measured in 12 h with an automated set up, after a day of sample preparation. The use of different standard materials and laser systems had no significant effect on method accuracy. Uncertainty on the measured (²³⁰Th/²³⁸U) activity ratios ranges from 5.4% to 7.6% for (²³⁰Th/²³⁸U) ratios equal to 0.7 and 0.1 respectively. Much of this uncertainty can be attributed to the heterogeneity of the standard material (²³⁰Th/²³⁸U) at the length scale of LA. A homogeneous standard material may therefore improve measurement uncertainty but is not a requirement for age-screening studies. The initial (²³⁴U/²³⁸U) of coral samples can be determined within ∼20‰, making it useful as a first indicator of open-system behaviour. For cold-water corals, success in determination of (²³²Th/²³⁸U) – which can affect final age accuracy – by LA depended strongly on sample heterogeneity. Age uncertainties (2 sigma) ranged from <0.8 ka at 0–10 ka, ∼1.5 ka at 20 ka to ∼15 ka at 125 ka. Thus, we have demonstrated that U-series dating by LA-MC-ICPMS can be usefully applied to a range of carbonate materials as a straightforward age-screening technique.     

Bioconcentration of the anionic surfactant linear alkylbenzene sulfonate (LAS) in the marine shrimp Palaemonetes varians: A radiotracer study

Uptake and depuration kinetics of dissolved [¹⁴C]C₁₂-6-linear alkylbenzene sulfonate (LAS) were determined in the shrimp Palaemonetes varians using environmentally relevant exposure concentration. The shrimp concentrated LAS from seawater with a mean BCF value of 120 L kg⁻¹ after a 7-day exposure. Uptake biokinetics were best described by a saturation model, with an estimated BCF_ss, of 159 ± 34 L kg⁻¹, reached after 11.5 days. Shrimp weight influenced significantly BCF value with smaller individuals presenting higher affinity to LAS. To the light of a whole body autoradiography, major accumulation of LAS occurred in the cephalothorax circulatory system (gills, heart, hepatopancreas) and ocular peduncle, but not in the flesh, limiting potential transfer to human consumers. LAS depuration rate constant value of the shrimp was 1.18 ± 0.08 d⁻¹ leading to less than 1% of remaining LAS in its tissues after 8 days of depuration.     

Fine chronology of volcanic processes using 238U-230Th systematics

The²³⁰Th-²³⁸U radioactive disequilibrium method was applied to the study of recent volcanic rocks from Costa Rica. Most samples are from the Irazu volcano. Some samples were dated by internal isochrons using the (²³⁰Th/²³²Th)-(²³⁸U/²³²Th) diagram, others were studied only by whole rock analyses. The evolution of the parent magma may be followed by the initial (²³⁰Th/²³²Th)₀ ratios of the rocks. A model involving a differentiating magma chamber that existed for 140,000 years under the Irazu volcano correlates well with the observations. Other volcanoes seem to be in earlier stages of their evolution. Continuing study may help to solve the tholeiitic to andesitic volcanism relationship.