Distribution of natural and anthropogenic radionuclides in northwest Mediterranean coastal sediments.

The distribution of radionuclides in NW Mediterranean coastal sediments, and the processes controlling their abundance were investigated in three cores taken near the island of Porquerolles and one offshore Monaco. The sediments collected near Porquerolles were strongly anoxic due to diagenetic processes involved in the decomposition of organic matter, whereas they transitioned from oxic to anoxic at a depth of 4 cm beneath the seawater interface at Monaco. Organic carbon (OC) was more abundant in sediments at Porquerolles (by about a factor of 3-5) than at Monaco and elsewhere in the coastal NW Mediterranean. Sediment cores collected NE of Porquerolles also possessed elevated uranium concentrations that correlated with high OC content and strong reducing conditions. The 239,240Pu and 241Am activities in surficial sediments ranged from 1 to 5.7 Bq kg-1 and 0.3 to 1 Bq kg-1, respectively, while the 137Cs activity ranged from 0.3 to 6.2 Bq kg-1. The mean activity ratios of 241Am/239,240Pu and 238Pu/239,240Pu in Porquerolles and Monaco sediments were similar to the global fallout ratios. Sediment inventories of global fallout 239,240Pu (430-800 Bq m-2) and 241Am (150-285 Bq m-2) were by about a factor of 5-10 higher at Porquerolles, whereas the inventory of 137Cs (430-1000 Bq m-2) was substantially lower at the investigated stations than have been reported elsewhere at similar latitudes. Specific local conditions characterised by high OC sediment loads due to the growth and mortality of Posidonia oceanica have been responsible for deposition of large amounts of seagrass tissues at the NE corner of Porquerolles, which have had a profound effect on the distribution of radionuclides in the sediments.

Impact of Saharan dust events on radionuclide levels in Monaco air and in the water column of the northwest Mediterranean Sea.

Characterization of atmospheric aerosols collected in Monaco (2004-2008) and in sediment traps at 200 m and 1000 m water depths at the DYFAMED (Dynamics of Atmospheric Fluxes in the Mediterranean Sea) station (2004) was carried out to improve our understanding of the impact of Saharan dust on ground-level air and on the water column. Activity concentrations of natural (210Pb, 210Po, uranium and radium isotopes) and anthropogenic (137Cs, 239Pu, 240Pu, and 239+240Pu) radionuclides and their isotopic ratios confirmed a Saharan impact on the investigated samples. In association with a large particulate matter deposition event in Monaco on 20 February 2004, the 137Cs (∼40 Bq kg-1) and 239+240Pu (∼1 Bq kg-1) activities were almost a factor of two higher than other Saharan deposition dust events. This single-day particle flux represented 72% of the annual atmospheric deposition in Monaco. The annual deposition of Saharan dust on the sea was 232-407 mBq m-2 for 137Cs and 6.8-9.8 mBq m-2 for 239+240Pu and contributed significantly (28-37% for 137Cs and 34-45% for 239+240Pu) to the total annual atmospheric input to the northwest Mediterranean Sea. The 137Cs/239+240Pu activity ratios in dust samples collected during different Saharan dust events confirmed their global fallout origin or mixing with local re-suspended soil particles. In the sediment trap samples the 137Cs activity varied by a factor of two, while the 239+240Pu activity was constant, confirming the different behaviors of Cs (dissolved) and Pu (particle reactive) in the water column. The 137Cs and 239+240Pu activities of sinking particles during the period of the highest mass flux collected in 20 February 2004 at the 200 m and 1000 m water depths represented about 10% and 15%, respectively, of annual deposition from Saharan dust events.

210Po/210Pb dynamics in relation to zooplankton biomass and trophic conditions during an annual cycle in northwestern Mediterranean coastal waters.

Monthly sampling in northwestern Mediterranean coastal waters was undertaken to better understand the relationship between zooplankton biomass and the cycling of the natural radionuclide (210)Po/(210)Pb pair during a one-year period (October 1995-November 1996). In conjunction with mesozooplankton collections and (210)Po/(210)Pb measurements in seawater, zooplankton and their fecal pellets, the biochemical composition of particulate organic matter (POM) was also examined at three depths (0, 20 and 50 m) as an indicator of trophic conditions. During May 1996, a strong zooplankton "bloom" was observed which was preceded by a prolonged increase in POM (protein + carbohydrates + lipids) starting at the end of March, and further demonstrated by a concomitant increase in the concentration of smaller particles, two features that are typical of mesotrophic waters. Simultaneous measurements of (210)Po in sea water and zooplankton showed an inverse trend between these two parameters during the sampling period, with the two lowest (210)Po concentrations in the dissolved phase of seawater coincident with the highest radionuclide concentrations in the zooplankton; however, this apparent relationship was not statistically significant over the entire year. Freshly excreted mesozooplankton and salp fecal pellets, which have been strongly implicated in the removal and downward transport of these radionuclides from the upper water column, contained (210)Po and (210)Pb levels ranging from 175 to 878 and 7.5-486 Bq kg(-1) dry weight, respectively. Salp pellets contained 5 and 10 times more (210)Po and (210)Pb than in fecal pellets produced by mixed zooplankton, a finding most likely related to their different feeding strategies. During the zooplankton biomass peak observed in May, the (210)Po concentration in zooplankton was at a minimum; however, in contrast to what has been reported to occur in some open sea oligotrophic waters, over the year no statistically significant inverse relationship was found between zooplankton biomass and (210)Po concentration in zooplankton. This observation may have resulted from the general lack of very low biomass concentrations (<1 mg m(-3)) measured in these coastal waters, biomass levels which commonly occur in open ocean oligotrophic regions.

Vertical fluxes of aromatic and aliphatic hydrocarbons in the Northwestern Mediterranean Sea.

Aliphatic and aromatic hydrocarbon fluxes were measured in time series sediment trap samples at 200 m and at 1000 m depths in the open Northwestern Mediterranean Sea, from December 2000 to July 2002. Averaged fluxes of n-alkanes, UCM and T-PAH(35) were 2.96 ± 2.60 µg m(-2) d(-1), 64 ± 60 µg m(-2) d(-1) and 0.68 ± 0.59 µg m(-2) d(-1), respectively. Molecular compositions of both hydrocarbon classes showed a contamination in petrogenic hydrocarbons well above the background levels of such an open site, whereas pyrolytic hydrocarbons stand in the range of other open Mediterranean locations. Fluxes displayed ample interannual and seasonal variabilities, mainly related to mass flux variation while concentration evolutions trigger secondary changes in pollutant fluxes. High lithogenic flux events exported particles with a larger pollutant load than biogenic particles formed during the spring bloom and during the summer. Sinking hydrocarbons were efficiently transported from 200 m to 1000 m.

Radiometric dating of sediment cores from a hydrothermal vent zone off Milos Island in the Aegean Sea.

Sediment cores from a hydrothermal vent zone off Milos Island in the Aegean Sea were dated using the 210Pb method. The average unsupported 210Pb inventory in the cores was calculated to be 3256 Bq m(-2). The corresponding mean annual 210Pb flux of 105 Bq m(-2) year(-1) is comparable to estimates of the atmospheric flux given in the literature. 210Pb fluxes calculated from the unsupported 210Pb inventories in cores are also comparable with the 210Pb vertical fluxes determined from settling particles off the coast of Milos Island. The highest unsupported 210Pb concentrations (89 Bq kg(-1)) were measured in the sediments nearest to the hydrothermal vent area suggesting that the sedimentation rate is lowest at this site. Direct gamma measurements of 210Pb were used to date three sediment cores that are located at different distances from the vent zone: one is in the immediate vicinity of the vent; and others are outside the zone. Sedimentation rates for these cores, calculated using the CRS and CIC models, ranged from 0.088+/-0.008 cm year(-1) to 0.14+/-0.01 cm year(-1). Where both models were applicable, the results given by the two methods were in good agreement. 137Cs concentrations in all three cores generally declined with depth but showed no clear signal of either the period of maximum fallout from weapons testing or the Chernobyl accident. 210Po activities were also measured and the maximum 210Po concentration was in the sediment surface layer (166 Bq kg(-1)).