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We present a study on the use of 239,240Pu as a chronostratigraphic marker to constrain 210Pb ages in young Holocene sediments from four coastal locations of Cuba (Caribbean Sea). The selected sites typify a variety of deposition environments such as a bay, a gulf, a coastal lagoon and a river estuary. The vertical distributions of 210Pb (and 226Ra), 239,240Pu and 137Cs in the sediment cores were determined in order to quantify the sedimentation processes. Mean activity ratios of 0.04 ± 0.01 for 238Pu/239,240Pu and 0.3 ± 0.2 for 241Am/239,240Pu indicated that atmospheric nuclear weapon tests (NWT) fallout was the main source of the anthropogenic radionuclides. Marine sites (Havana Bay and Gulf of Batabano) were characterized by low or negligible signals of 137Cs, which impeded its use as a chronostratigraphic marker. In the Sagua River Estuary and the Guanaroca Lagoon, where mixing of fresh and saline waters take place, depth profiles of 137Cs and 239,240Pu were in good agreement. A simple model that assumes a well-mixed reservoir in surface ocean waters and constant sediment accumulation was used to interpret the 239,240Pu profiles. The model corroborated the 210Pb ages, except in the case of the highly mixed sediment cores from the Gulf of Batabano. The apparent mean residence time of 239,240Pu in the well-mixed reservoir ranges from 5 to 50 years, with longer timescales for marine sites. 239,240Pu showed to be a useful time tracer in coastal sediments where the 137Cs signal is very low. [ABSTRACT FROM AUTHOR]

Abstract: Environmental archives, such as sediments, banded corals and tree rings, are widely used to reconstruct past environmental conditions of ecosystems. In particular, 210Pb has been used during more than 4 decades, through dating of undisturbed sediment cores, to study ecosystem changes during the last 100yr. Since its inception, diverse dating models have been proposed, developed, used and validated in numerous environments, but their nomenclature and formulation is not homogenous. In this work we emphasize that conceptual models used to date undisturbed sediment cores can be deduced from a single fundamental equation, which relates excess 210Pb concentration in sediment, its flux to the sediment surface and mass accumulation rate. From this equation, models were consistently named based on the main hypothesis used and, using a unified and logical nomenclature, dating equations were derived in detail. We applied in detail most of the described models to a sediment core from Mexico and uncertainty expressions were also included. Finally, some recommendations to use the models are proposed. We believe that this work can facilitate the use of 210Pb as a tool to date sediment cores in a more homogeneous way. [Copyright &y& Elsevier]

Abstract: During the reoccupation of the WOCE transect A10 at 30°S by the BEAGLE2003 cruise, the SHOTS project partners collected a large number of samples for the analysis of isotopic tracers. 137Cs was mostly deposited on the oceans surface during the late 1950s and early 1960s, after the atmospheric detonation of large nuclear devices, which mostly occurred in the Northern Hemisphere. The development of advanced radioanalytical and counting techniques allowed to obtain, for the first time in this region, a zonal section of 137Cs water concentrations, where little information existed before, thus constituting an important benchmark for further studies. 137Cs concentrations in the upper waters (0–1000m) of the south-eastern Atlantic Ocean are similar to those observed in the south-western Indian Ocean, suggesting transport of 137Cs labeled waters by the Agulhas current to the Benguela Current region. In contrast, bomb radiocarbon data do not show this feature, indicating the usefulness of 137Cs as a radiotracer of water mass transport from the Indian to the South Atlantic Ocean. [Copyright &y& Elsevier]

Abstract: The vertical distribution of Hg and Pb were determined in a sediment core collected from the Sagua estuary (North Cuba) that receives input from the Sagua river, one of the most polluted rivers discharging into the Cuban coastal environment. Depth profiles of metal concentrations were converted to time-based profiles using the 210Pb dating method and confirmed with the 137Cs fallout peak. The mean mass accumulation rate was estimated to be 0.17±0.04gcm−2 y−1 (mean sediment accumulation rate 0.52±0.13cmy−1) and the core bottom was estimated to date back about 130years. The historical sedimentary record showed a strong enrichment of mercury concentrations in the past decades, caused by the incomplete treatment of industrial wastes from a chlor-alkali plant with mercury-cell technology in the Sagua river basin. Lead fluxes to sediments showed a gradual increase from the 1920s to present, which agrees with a population increase in Sagua la Grande City. Fluxes of both metals have increased the past 25years, with values reaching a maximum of 0.5 and 3.9μgcm−2 y−1 for Hg and Pb, respectively. [Copyright &y& Elsevier]

A reference material designed for the determination of anthropogenic and natural radionuclides in sediment, IAEA-384 (Fangataufa Lagoon sediment), is described and the results of certification are presented. The material has been certified for 8 radionuclides (40K, 60Co, 155Eu, 230Th, 238U, 238Pu, 239+240Pu and 241Am). Information values are given for 12 radionuclides (90Sr, 137Cs, 210Pb (210Po), 226Ra, 228Ra, 232Th, 234U, 235U, 239Pu, 240Pu and 241Pu). Less reported radionuclides include 228Th, 236U, 239Np and 242Pu. The reference material may be used for quality management of radioanalytical laboratories engaged in the analysis of radionuclides in the environment, as well as for the development and validation of analytical methods and for training purposes. The material is available from IAEA in 100 g units. [ABSTRACT FROM AUTHOR]

210Pb was analysed in samples collected from (16) sediment traps, deployed during 1 year on the Northwestern Mediterranean continental margins, within the framework of the (MTP I)-EUROMARGE-NB programme. The traps were moored within (5) submarine canyons and their adjacent open slope, corresponding to contrasting conditions of particle inputs (fluxes and constituents). The major meso-scale observation (at the margin) is the variation in 210Pb fluxes along the slope, increasing by a factor of 2–3 between the entrance and the exit of the slope, in relation to the general (water) circulation. At a smaller scale (canyon), the 210Pb fluxes showed trends which were common to the various sites, i.e. a seaward decrease at 500 m depth and an increase, with depth, in the canyons. All these features are related to mass flux variations, except for periods with huge mass fluxes, when 210Pb fluxes reached a constant value. 210Pb activities decreased with increasing mass flux; then did not show clear relationship with the concentration of the major constituents of the flux.210Pb fluxes, obtained from the traps were mainly in excess of the theoretical 210Pb flux, available in the overlying water column. Since 210Pb inventories, measured on the basis of the shelf and slope bottom sediments, were also in excess in relation to the available flux. The margin, as a whole, appears as a sink for 210Pb. This boundary-scavenging process appears to be controlled completely by the mass flux of particles. Differences were observed between 210Pb fluxes in the near-bottom traps and in the underlying sediments; there can be linked to mass flux and/or morphobathymetry (the trap flux is higher than the sediment flux in the canyon, but lower on the open slope). Overall, the differences were not in excess of 50%, confirming good representation of data collected by the sediment traps. However, this finding must be taken into account when comparing organic carbon or other constituent fluxes, between the traps and the sediment. [Copyright &y& Elsevier]

Abstract: The accumulation, enrichment and provenance of selected trace metals (Ag, As, Cd, Cr, Cu, Hg, Ni, Pb, V and Zn) were studied in sediment cores collected from three lakes located in the Central Mexican Plateau, selected on the basis of their contrasting degree of urbanization: Santa Elena Lake, in a rural and remote area; El Tule Lake, in a rural and slightly urbanized area; and Chapala Lake, in a highly urbanized area. Grain size, magnetic susceptibility and sedimentary constituents such as organic carbon, calcium carbonate, as well as major (Al, Fe, Mn) and minor (Ca, Li, Rb, Sr, Th) elements were analyzed to explain the concentration trends of trace metals. Factor analysis (FA) was used to assess the provenance of the trace elements. The highest metal enrichment factor (EF) above natural concentration levels was found at Chapala Lake for Ag (EF=3.9), although other trace element EF in all lakes was <2.0, indicating slight contamination. However, the concentration levels of Cr and Ni in all lakes, Hg and Zn in Chapala Lake, Cu in El Tule Lake and As in Santa Elena Lake were above international benchmarks for which adverse effects are expected to occur frequently, even for those metals only slightly enriched (e.g. As, Cr). Through FA, the terrigenous contribution was identified as the most important source of trace metals to the three lakes, most likely related to deforestation and erosion of the surrounding areas, followed by atmospheric transport of volcanic ashes, rather than to direct sources. [Copyright &y& Elsevier]

The present plutonium and 137Cs concentrations in South Pacific Ocean surface waters were determined. The water samples were collected in the South Pacific mid-latitude region (32.5 °S) during the BEAGLE expedition conducted in 2003–04 by JAMSTEC. 239,240Pu concentrations in surface seawater of the South Pacific were in the range of 0.5 to 4.1 mBq m−3, whereas 137Cs concentrations ranged from 0.07 to 1.7 Bq m−3. The observed 239,240Pu and 137Cs concentrations in the South Pacific were almost of the same level as those in the North Pacific subtropical gyre. The surface 239,240Pu in the South Pacific subtropical gyre showed larger spatial variations than 137Cs, as it may be affected by physical and biogeochemical processes. The 239,240Pu/137Cs activity ratios, which reflect biogeochemical processes in seawater, were generally smaller than that observed in global fallout, except for the most eastern station. The 239,240Pu/137Cs ratios in the South Pacific tend to be higher than that in the North Pacific. The relationships between anthropogenic radionuclides and oceanographic parameters such as salinity and nutrients were examined. The 137Cs concentrations in the western South Pacific (the Tasman Sea) and the eastern South Pacific were negatively correlated with the phosphate concentration, whereas there is no correlation between the 137Cs and nutrients concentrations in the South Pacific subtropical gyre. The mutual relationships between anthropogenic radionuclides and oceanographic parameters are important for better understanding of transport processes of anthropogenic radionuclides and their fate in the South Pacific. [Copyright &y& Elsevier]