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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]

The 210Pb sediment dating is the most widely used method to determine recent (~100–150 years) chronologies and sediment accumulation rates in aquatic environments and has been used effectively for reconstruction of diverse environmental processes associated with global change. Owing to the relative accessibility of the 210Pb methodology, many environmental chronologies have been produced, but not always critically assessed. Sometimes, sedimentary processes such as compaction, local mixing, erosion, or episodic sedimentation are not taken into account, nor the validity of the fundamental premises and proper estimation of uncertainties assessed. A Pb-210 dating interlaboratory comparison modelling exercise was designed within the framework of the IAEA (International Atomic Energy Agency) Coordinated Research Project "Study of temporal trends of pollution in selected coastal areas by the application of isotopic and nuclear tools" (CRP K41016), to identify potential problems associated with the use of 210Pb dating models and to suggest best practices to obtain reliable reconstructions. The exercise involved 14 laboratories worldwide with different levels of expertise in the application of the 210Pb dating methods. The dating exercise was performed using 210Pb, 226Ra and 137Cs activity data from two sediment cores (coastal and lacustrine sediments), and the participants were requested to provide their 210Pb chronologies based on dating models. This modelling exercise evidenced the limitations and constraints of 210Pb method when supplementary and validation information is not available. The exercise highlighted the relevance of solid understanding of the fundamentals, assumptions and limitations of the 210Pb dating method and its validation, and allowed identifying key aspects to improve the reliability of 210Pb dating process, including: a critical examination and interpretation of the 210Pb activity depth profile; an appropriate selection of the 210Pb dating model according to the characteristics of the 210Pb activity profile and the environmental setting taking into account sediment compaction in the calculations; a sound identification of the 210Pb equilibrium depth and the estimation of the 210Pb inventory ensuring the best possible estimation of interpolated 210Pb values when needed; and the use of independent markers to corroborate the age models. • Potential constraints and limitations of the 210Pb dating method are evidenced. • The 210Pb dating method is far to be a straightforward tool for dating sediment cores. • Reliable 210Pb chronologies require a proper understanding of the dating methodology. [ABSTRACT FROM AUTHOR]

Abstract: Since 1998 the highly polluted Havana Bay ecosystem has been the subject of a mitigation program. In order to determine whether pollution-reduction strategies were effective, we have evaluated the historical trends of pollution recorded in sediments of the Bay. A sediment core was dated radiometrically using natural and artificial fallout radionuclides. An irregularity in the 210Pb record was caused by an episode of accelerated sedimentation. This episode was dated to occur in 1982, a year coincident with the heaviest rains reported in Havana over the XX century. Peaks of mass accumulation rates (MAR) were associated with hurricanes and intensive rains. In the past 60 years, these maxima are related to strong El Niño periods, which are known to increase rainfall in the north Caribbean region. We observed a steady increase of pollution (mainly Pb, Zn, Sn, and Hg) since the beginning of the century to the mid 90s, with enrichment factors as high as 6. MAR and pollution decreased rapidly after the mid 90s, although some trace metal levels remain high. This reduction was due to the integrated coastal zone management program introduced in the late 90s, which dismissed catchment erosion and pollution. [Copyright &y& Elsevier]

Artificial radionuclides enter the Mediterranean Sea mainly through atmospheric deposition following nuclear weapons tests and the Chernobyl accident, but also through the river discharge of nuclear facility effluents. Previous studies of artificial radionuclides impact of the Mediterranean Sea have focussed on shallow, coastal sediments. However, deep sea sediments have the potential to store and accumulate pollutants, including artificial radionuclides. Deep sea marine sediment cores were collected from Mediterranean Sea abyssal plains (depth >2000 m) and analysed for 239,240Pu and 137Cs to elucidate the concentrations, inventories and sources of these radionuclides in the deepest areas of the Mediterranean. The activity — depth profiles of 210Pb, together with 14C dating, indicate that sediment mixing redistributes the artificial radionuclides within the first 2.5 cm of the sedimentary column. The excess 210Pb inventory was used to normalize 239,240Pu and 137Cs inventories for variable sediment fluxes. The 239,240Pu/210Pb xs ratio was uniform across the entire sea, with a mean value of 1.24×10−3, indicating homogeneous fallout of 239,240Pu. The 137Cs/210Pb xs ratio showed differences between the eastern (0.049) and western basins (0.030), clearly significant impact of deep sea sediments from the Chernobyl accident. The inventory ratios of 239,240Pu/137Cs were 0.041 and 0.025 in the western and eastern basins respectively, greater than the fallout ratio, 0.021, showing more efficient scavenging of 239,240Pu in the water column and major sedimentation of 137Cs in the eastern basin. Although areas with water depths of >2000 m constitute around 40% of the entire Mediterranean basin, the sediments in these regions only contained 2.7% of the 239,240Pu and 0.95% of the 137Cs deposited across the Sea in 2000. These data show that the accumulation of artificial radionuclides in deep Mediterranean environments is much lower than predicted by other studies from the analysis of continental shelf sediments. [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]