Thorium isotopes as tracers of particles dynamics and deep water circulation in the Indian sector of the Southern Ocean (ANTARES IV)

Dissolved and particulate samples were collected to study the distribution of thorium isotopes (²³⁴Th, ²³²Th and ²³⁰Th) in the water column of the Indian sector of the Southern Ocean (from 42°S to 47°S and from 60°E to 66°E, north of the Polar Front) during Austral summer 1999. Vertical profiles of excess ²³⁰Th (²³⁰Th_xs) increases linearly with depth in surface water (0–100 m) and a model was applied to estimate a residence time relative to the thorium scavenging (τ_scav). Low τ_scav in the Polar Front Zone (PFZ) are found, compared to those estimated in the Subtropical Front Zone (STZ). Changes in particle composition between the PFZ and STZ could influence the ²³⁰Th_xs scavenging efficiency and explain this difference. An innovative coupling between ²³⁴Th and ²³⁰Th_xs was then used to simultaneously constrain the settling velocities of small (0.6–60 μm) and large (above 60 μm) particles. Although the different hydrological and biogeochemical regimes visited during the ANTARES IV cruise did not explain the spatial variation of sinking velocity estimates, our results indicate that less particles may reach the seafloor north (60 ± 2 m d^− 1, station 8) than south of the Agulhas Return Current (119 ± 23 and 130 ± 5 m d^− 1 at stations 3 and 7, respectively). This information is essential for understanding particle transport and by extension, carbon export. In the deep water column, the ²³⁰Th_xs concentrations did not increase linearly with depth, probably due to lateral transport of North Atlantic Deep Water (NADW) from the Atlantic to the Indian sector, which renews the deep waters and decreases the ²³⁰Th_xs concentrations. A specific ²³⁰Th_xs transport model is applied in the deep water column and allows us to assess a “travel time” of NADW ranging from 2 to 15 years.     

Isotopic,trace element and nutrient characterization of coastal waters from Ubatuba inner shelf area,south-eastern Brazil

Stable isotopes, tritium, radium isotopes, radon, trace elements and nutrients data were collected during two sampling campaigns in the Ubatuba coastal area (south-eastern Brazil) with the aim of investigating submarine groundwater discharge (SGD) in the region. The isotopic composition (δD, δ¹⁸O, ³H) of submarine waters was characterised by significant variability and heavy isotope enrichment. The stable isotopes and tritium data showed good separation of groundwater and seawater groups. The contribution of groundwater in submarine waters varied from a few % to 17%. Spatial distribution of ²²²Rn activity concentration in surface seawater revealed changes between 50 and 200 Bq m⁻³ which were in opposite relationship with observed salinities. Time series measurements of ²²²Rn activity concentration in Flamengo Bay (from 1 to 5 kBq m⁻³), obtained by in situ underwater gamma-spectrometry showed a negative correlation between the ²²²Rn activity concentration and tide/salinity. This may be caused by sea level changes as tide effects induce variations of hydraulic gradients, which increase ²²²Rn concentration during lower sea level, and opposite, during high tides where the ²²²Rn activity concentration is smaller. The estimated SGD fluxes varied during 22–26 November between 8 and 40 cm d⁻¹, with an average value of 21 cm d⁻¹ (the unit is cm³/cm² per day). The radium isotopes and nutrient data showed scattered distributions with offshore distance and salinity, which implies that in a complex coast with many small bays and islands, the area has been influenced by local currents and groundwater–seawater mixing. SGD in the Ubatuba area is fed by coastal contaminated groundwater and re-circulated seawater (with small admixtures of groundwater), which claims for potential environmental concern with implications on the management of freshwater resources in the region.     

Cosmogenic radionuclides and mineralogical properties of the Chelyabinsk (LL5) meteorite: What do we learn about the meteoroid?

On February 15, 2013, after the observation of a brilliant fireball and a spectacular airburst over the southern Ural region (Russia), thousands of stones fell and were rapidly recovered, bringing some extremely fresh material for scientific investigations. We undertook a multidisciplinary study of a dozen stones of the Chelyabinsk meteorite, including petrographic and microprobe investigations to unravel intrinsic characteristics of this meteorite. We also study the short and long‐lived cosmogenic radionuclides to characterize the initial meteoroid size and exposure age. Petrographic observations, as well as the mineral compositions obtained by electron microprobe analyses, allow us to confirm the classification of the Chelyabinsk meteorite as an LL5 chondrite. The fragments studied, a few of which are impact melt rocks, contain abundant shock melt veins and melt pockets. It is likely that the catastrophic explosion and fragmentation of the Chelyabinsk meteoroid into thousands of stones was in part determined by the initial state of the meteoroid. The radionuclide results obtained show a wide range of concentrations of ¹⁴C, ²²Na, ²⁶Al, ⁵⁴Mn, ⁵⁷Co, ⁵⁸Co, and ⁶⁰Co, which indicate that the pre‐atmospheric object had a radius >5 m, consistent with other size estimates based on the magnitude of the airburst caused by the atmospheric entry and breakup of the Chelyabinsk meteoroid. Considering the observed ²⁶Al activities of the investigated samples, Monte Carlo simulations, and taking into account the ²⁶Al half‐life (0.717 Myr), the cosmic‐ray exposure age of the Chelyabinsk meteorite is estimated to be 1.2 ± 0.2 Myr. In contrast to the other radionuclides, ¹⁴C showed a very large range only consistent with most samples having been exposed to anthropogenic sources of ¹⁴C, which we associate with radioactive contamination of the Chelyabinsk region by past nuclear accidents and waste disposal, which has also been confirmed by elevated levels of anthropogenic ¹³⁷Cs and primordial ⁴⁰K in some of the Chelyabinsk fragments.     

Summary of IAEA-MEL's investigation of Kara Sea radioactivity and radiological assessment

IAEA-MEL participated in five expeditions to the Kara Sea with the aim of assessing the radiological consequences of dumped radioactive wastes in the Novaya Zemlya Bays and Trough. The programme included sampling, in-situ underwater investigations, laboratory analyses of water, sediment and biota samples, the development of a marine radioactivity database, modelling and radiological assessment, the organization of intercomparison exercises and the evaluation of distribution coefficients. Radiometric investigations have shown that no radiologically significant environmental contamination has occurred. Leakages which have led to locally increased levels of radionuclides in sediment have only been observed in Stepovoy and Abrosimov Bays. Computer modelling results suggest that only radiological effects on local and regional scales may be of importance. The global radiological impact of the disposals in the Arctic Seas will be negligible.     

The history of the Tissint meteorite,from its crystallization on Mars to its exposure in space: New geochemical,isotopic, and cosmogenic nuclide data

The Tissint meteorite fell on July 18, 2011 in Morocco and was quickly recovered, allowing the investigation of a new unaltered sample from Mars. We report new high‐field strength and highly siderophile element (HSE) data, Sr‐Nd‐Hf‐W‐Os isotope analyses, and data for cosmogenic nuclides in order to examine the history of the Tissint meteorite, from its source composition and crystallization to its irradiation history. We present high‐field strength element compositions that are typical for depleted Martian basalts (0.174 ppm Nb, 17.4 ppm Zr, 0.7352 ppm Hf, and 0.0444 ppm W), and, together with an extended literature data set for shergottites, help to reevaluate Mars’ tectonic evolution in comparison to that of the early Earth. HSE contents (0.07 ppb Re, 0.92 ppb Os, 2.55 ppb Ir, and 7.87 ppb Pt) vary significantly in comparison to literature data, reflecting significant sample inhomogeneity. Isotope data for Os and W (¹⁸⁷Os/¹⁸⁸Os = 0.1289 ± 15 and an ε¹⁸²W = +1.41 ± 0.46) are both indistinguishable from literature data. An internal Lu‐Hf isochron for Tissint defines a crystallization age of 665 ± 74 Ma. Considering only Sm‐Nd and Lu‐Hf chronometry, we obtain, using our and literature values, a best estimate for the age of Tissint of 582 ± 18 Ma (MSWD = 3.2). Cosmogenic radionuclides analyzed in the Tissint meteorite are typical for a recent fall. Tissint's pre‐atmospheric radius was estimated to be 22 ± 2 cm, resulting in an estimated total mass of 130 ± 40 kg. Our cosmic‐ray exposure age of 0.9 ± 0.2 Ma is consistent with earlier estimations and exposure ages for other shergottites in general.     

Radionuclides as tracers of water fronts in the South Indian Ocean—ANTARES IV Results

Anthropogenic ⁹⁰Sr, ^239,240Pu and ²⁴¹Am were used as tracers of water mass circulation in the Crozet Basin of the South Indian Ocean, represented by three main water fronts—Agulhas (AF), Subtropical (STF) and Subantarctic (SAF). Higher ⁹⁰Sr concentrations observed north of 43°S were due to the influence of AF and STF, which are associated with the south branch of the Subtropical gyre, which acts as a reservoir of radionuclides transported from the North to the South Indian Ocean. On the other hand, the region south of 43°S has been influenced by SAF, bringing to the Crozet Basin Antarctic waters with lower radionuclide concentrations. The ²³⁸Pu/^239,240Pu activity ratios observed in water and zooplankton samples indicated that, even 35 years after the injection of ²³⁸Pu to the Indian Ocean from the burn-up of the SNAP-9A satellite, the increased levels of ²³⁸Pu in surface water and zooplankton are still well visible. The radionuclide concentrations in seawater and their availability to zooplankton are responsible for the observed ²¹⁰Po, ^239,240Pu and ²⁴¹Am levels in zooplankton.     

Anthropogenic Radionuclides in the Caspian Sea

Analysis and interpretation of the distribution of anthropogenic radionuclides ⁹⁰Sr, ¹³⁷Cs, and ^239,240Pu in the Caspian Sea water are presented. These radionuclides are shown to be of environmental importance and to be useful for studying water mass dynamics.