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.     

Differential concentration of Technetium-99 (99Tc) in common intertidal molluscs with different food habits

Concentration of ⁹⁹Tc has been measured in fucoids and molluscs, sampled in a sheltered intertidal at the southwest coast of Norway from February to November 2006. The concentrations of ⁹⁹Tc in molluscs differed significantly between species. The filtering bivalve Mytilus edulis had the lowest concentrations with averages of 2.3-5.9 Bq kg⁻¹ d.w., while the herbivorous gastropods Littorinalittorina, Littorina obtusata and Patella vulgata had higher concentrations. P. vulgata and L. obtusata had the highest concentrations, 40-47 and 26-30 Bq kg⁻¹ d.w., respectively. L. obtusata has a specialized habit of living, and prefers to feed on fucoids. P. vulgata can graze extensively on the fucoid Ascophyllum nodosum when available. Fucoids are known to have very high uptake of ⁹⁹Tc, and this was also found in the present study. The high ⁹⁹Tc-concentrations of L. obtusata and P. vulgata are most likely due to their habit of feeding on fucoids.     

Accumulation,solid partitioning and remobilisation of 99Tc in subtidal and intertidal sediments in the Irish Sea

Recent studies have shown that accumulation of ⁹⁹Tc in seabed sediments labelled by authorised radioactive liquid discharges into the NE Irish Sea from the Sellafield reprocessing complex is greater than previously thought. In this paper, new data on ⁹⁹Tc concentration profiles in subtidal and intertidal sediments from the eastern and western Irish Sea are provided with a view to elucidating the processes responsible for the incorporation and retention of ⁹⁹Tc in the seabed. The data show that substantial amounts of ⁹⁹Tc have accumulated in the fine-grained subtidal sediments off the Cumbrian coast, particularly after increased releases from Sellafield following the commissioning of the Enhanced Actinide Removal Plant (EARP) in 1994. In all the cores taken in this area, ⁹⁹Tc has been found to be present to depths in excess of 30 cm. Analysis of ¹³⁷Cs and ²⁴¹Am profiles, together with other supporting geochemical data, show a high degree of homogenisation of the sediments down to these depths as a result of physical and biological processes, and confirm that incorporation of ⁹⁹Tc into the sediment compartment is actually the result of mixing and reworking, rather than active sediment accumulation. In contrast, active deposition of material transported from this mixed pool of sediment appears to be the dominant mechanism controlling ⁹⁹Tc profiles in intertidal areas close to the Sellafield discharge outfall.Data obtained from the analysis of subtidal sediment cores from the western Irish Sea mud basin suggest that similar mixing processes to those occurring in the subtidal sediments of the eastern Irish Sea are also active in this area. Time-series data on ⁹⁹Tc concentrations in surficial sediments from this basin, gathered in the period 1988–2004, inclusive, show a clear increase in concentrations, by a factor of ～2, between samples collected pre-EARP and post-EARP. The constancy of ⁹⁹Tc concentrations in surface sediments throughout the 1980s and the early-1990s suggests that little redissolution and export of ⁹⁹Tc occurred over this extended period. A similar observation applies to the post-EARP period, when concentrations remained relatively constant despite the reported steady decrease in ⁹⁹Tc concentrations in the overlying waters.This apparent lack of remobilisation is consistent with data from sequential extraction analyses, which indicate that the bulk of the ⁹⁹Tc is strongly bound to non-labile geochemical phases, with only a small proportion associated with exchangeable and acido-soluble phases. Further, these analyses show that ⁹⁹Tc is not associated with oxygen-sensitive and highly-reactive acid-volatile sulphides (AVS) to any significant extent.     

Groundwater-derived contaminant fluxes along a channelized Coastal Plain stream

Recent studies in various settings across eastern North America have examined the movement of volatile organic compound (VOC) plumes from groundwater to streams, but few studies have addressed focused discharge of such plumes in unlithified sediments. From 1999 through 2002, we monitored concentrations of trichloroethene (TCE) and the non-volatile co-contaminant technetium-99 (⁹⁹Tc) along Little Bayou Creek, a first-order perennial stream in the Coastal Plain of western Kentucky. Spring flow contributed TCE and ⁹⁹Tc to the creek, and TCE concentrations tended to vary with ⁹⁹Tc in springs. Contaminant concentrations in stream water fluctuated seasonally, but not always synchronously with stream flow. However, contaminant influxes varied seasonally with stream flow and were dominated by a few springs. Concentrations of O₂, , and , values of δ³⁷Cl_DOCl in groundwater, and the lack of less-chlorinated ethenes in groundwater and stream water indicated that anaerobic biodegradation of TCE was unlikely. Losses of TCE along Little Bayou Creek resulted mainly from volatilization, in contrast to streams receiving diffuse contaminated discharge, where intrinsic bioremediation of VOCs appears to be prevalent.     

Bioaccumulation and trophic transfer of polybrominated diphenyl ethers (PBDEs) in a marine food web from Liaodong Bay,North China

The concentrations of 21 polybrominated diphenyl ethers (PBDEs) congeners were analyzed in organisms within a marine food web collected from the Liaodong Bay, North China. The total concentrations of PBDEs in all samples ranged from 0.87 to 91.4 ng g⁻¹ lipid weight (lw). BDE-47 was the predominant congener and had a concentration ranging from 0.30 to 36.1 ng g⁻¹ lw. The trophic magnification factors (TMF) of the PBDEs were calculated using the trophic levels obtained from the stable nitrogen isotope ratios. The TMF value of ∑PBDEs was 3.50 for the entire food web and 2.21 for the food web excluding seabirds. Four concentration ratios, BDE-99/BDE-100, BDE-99/BDE-47, BDE-153/BDE-154 and BDE-183/BDE-154, decreased linearly with the increase of the trophic levels in the invertebrates and the fishes (p < 0.01). The results suggested that the PBDEs were steadily metabolized in the trophic transfer process along the food chain.     

Carbon isotopic compositions of organic matter across continental Cretaceous–Tertiary (K–T) boundary sections: Implications for paleoenvironment after the K–T impact event

To assess the environmental perturbation induced by the impact event that marks the Cretaceous–Tertiary (K–T) boundary, concentrations and isotopic compositions of bulk organic carbon were determined in sedimentary rocks that span the terrestrial K–T boundary at Dogie Creek, Montana, and Brownie Butte, Wyoming in the Western Interior of the United States. The boundary clays at both sites are not bounded by coals. Although coals consist mainly of organic matter derived from plant tissue, siliceous sedimentary rocks, such as shale and clay, may contain organic matter derived from microbiota as well as plants. Coals record δ¹³C values of plant-derived organic matter, reflecting the δ¹³C value of atmospheric CO₂, whereas siliceous sedimentary rocks record the δ¹³C values of organic matter derived from plants and microbiota. The microbiota δ¹³C value reflects not only the δ¹³C value of atmospheric CO₂, but also biological productivity. Therefore, the siliceous rocks from these sites yields information that differs from that obtained previously from coal beds.Across the freshwater K–T boundary at Brownie Butte, the δ¹³C values decrease by 2.6‰ (from − 26.15‰ below the boundary clay to − 28.78‰ above the boundary clay), similar to the trend in carbonate at marine K–T sites. This means that the organic δ¹³C values reflect the variation of δ¹³C of atmospheric CO₂, which is in equilibrium with carbon isotopes at the ocean surface. Although a decrease in δ¹³C values is observed across the K–T boundary at Dogie Creek (from − 25.32‰ below the boundary clay to − 26.11‰ above the boundary clay), the degree of δ¹³C-decrease at Dogie Creek is smaller than that at Brownie Butte and that for marine carbonate.About 2‰ decrease in δ¹³C of atmospheric CO₂ was expected from the δ¹³C variation of marine carbonate at the K–T boundary. This δ¹³C-decrease of atmospheric CO₂ should affect the δ¹³C values of organic matter derived from plant tissue. As such a decrease in δ¹³C value was not observed at Dogie Creek, a process that compensates the δ¹³C-decrease of atmospheric CO₂ should be involved. For example, the enhanced contribution of ¹³C-enriched organic matter derived from algae in a high-productivity environment could be responsible. The δ¹³C values of algal organic matter become higher than, and thus distinguishable from, those of plant organic matter in situations with high productivity, where dissolved HCO₃⁻ becomes an important carbon source, as well as dissolved CO₂. As the δ¹³C-decrease of atmospheric CO₂ reflected a reduction of marine productivity, the compensation of the δ¹³C decrease by the enhanced activity of the terrestrial microbiota means that the microbiota at freshwater environment recovered more rapidly than those in the marine environment.A distinct positive δ¹³C excursion of 2‰ in the K–T boundary clays is superimposed on the overall decreasing trend at Dogie Creek; this coincides with an increase in the content of organic carbon. We conclude that the K–T boundary clays include ¹³C-enriched organic matter derived from highly productive algae. Such a high biological productivity was induced by phenomena resulting from the K–T impact, such as nitrogen fertilization and/or eutrophication induced by enhanced sulfide formation. The high productivity recorded in the K–T boundary clays means that the freshwater environments (in contrast to marine environments) recovered rapidly enough to almost immediately (within 10 yr) respond to the impact-related environmental perturbations.     

The application of lead isotope ratios in the Antarctic macroalga Iridaea cordata as a contaminant monitoring tool

Lead (Pb) isotope ratios were measured in the marine macroalga Iridaea cordata collected from four locations in the Windmill Islands, East Antarctica. Based on the masses of thalli collected, samples analysed in this study were likely to be a mixture of one and two year old thalli. For a sample of thalli of various ages (<12 months to 2 years old) from the same site there was no apparent variation in Pb concentration or Pb isotope ratio with thallus mass/age, indicating that contaminant sources had been constant over the lifetime of the thalli sampled. I.cordata samples close to the Thala Valley waste disposal site (Brown Bay Inner) near the Australian Station, Casey, displayed isotopic signatures (²⁰⁸Pb/²⁰⁴Pb 35.99; ²⁰⁶Pb/²⁰⁷Pb 1.066; n = 3; average values shown) trending towards that possessed by major Australian Pb sources (Broken Hill and Mt Isa, ²⁰⁸Pb/²⁰⁴Pb 35.60; ²⁰⁶Pb/²⁰⁷Pb 1.041) suggesting that these samples had been exposed to anthropogenic Pb originating from the Thala Valley waste disposal site. Material collected hundreds of metres from the tip location at Brown Bay Outer had isotopic values (²⁰⁸Pb/²⁰⁴Pb 36.32; ²⁰⁶Pb/²⁰⁷Pb 1.088; n = 10) intermediate between Brown Bay Inner and sites further from the contaminant source at Sparkes Bay and Wilkes (²⁰⁸Pb/²⁰⁴Pb 36.46; ²⁰⁶Pb/²⁰⁷Pb 1.094; n = 4) showing that contaminant transport was predominantly restricted to Brown Bay Inner. This study demonstrates that the isotope ratios of Pb in marine macroalgae can provide valuable information as to the origin and extent of heavy metal flux in a marine environment.     

A comparative study of toxicity identification using Daphnia magna and Tigriopus japonicus: Implications of establishing effluent discharge limits in Korea

In Korea, the new permission criteria for industrial effluents based on Daphnia magna acute toxicity tests will be gradually implemented starting from 2011. Thus, in this study, toxicity assessment and identification using a marine species (Tigriopus japonicus) and the freshwater species (D. magna) was comparatively investigated. Effluent from an acid mine drainage treatment plant showed acute toxicity toward both organisms due to low pH, which was removed by neutralization of the effluent. Additionally, evaluation of the effluent of an electronics company revealed that Cu was attributable to the observed toxicity, and the effluent was more toxic toward T. japonicus than D. magna. Moreover, effluents from a metal plating factory were acutely toxic toward D. magna (6.50 TU), while they were not toxic against T. japonicus. Toxicity identification revealed that the high level of Cl⁻ (12,841 mg L⁻¹) was the cause of toxicity. Thus, the effluents had no effect on the marine species, T. japonicus. These findings suggest that a marine species rather than a freshwater species is more desirable for toxicity assessment of industrial effluent discharged into the saltwater, and thus should be considered in the legislation of toxicity-based discharge limits in Korea.     

Toxicities of antifouling biocide Irgarol 1051 and its major degraded product to marine primary producers

Irgarol 1051 (2-methythiol-4-tert-butylamino-6-cyclopropylamino-s-triazine) is an algaecide commonly used in antifouling paints. It undergoes photodegradation which yields M1 (2-methylthio-4-tert-butylamino-6-amino-s-triazine) as its major and most stable degradant. Elevated levels of both Irgarol and M1 have been detected in coastal waters worldwide; however, ecotoxicity effects of M1 to various marine autotrophs such as cyanobacteria are still largely unknown. This study firstly examined and compared the 96 h toxicities of Irgarol and M1 to the cyanobacterium Chroococcus minor and two marine diatom species, Skeletonema costatum and Thalassiosira pseudonana. Our results suggested that Irgarol was consistently more toxic to all of the three species than M1 (96 h EC50 values: C. minor, 7.71 μg L⁻¹ Irgarol vs. >200 μg L⁻¹ M1; S. costatum, 0.29 μg L⁻¹ Irgarol vs. 11.32 μg L⁻¹ M1; and T. pseudonana, 0.41 μg L⁻¹ Irgarol vs. 16.50 μg L⁻¹ M1). Secondly, we conducted a meta-analysis of currently available data on toxicities of Irgarol and M1 to both freshwater and marine primary producers based on species sensitivity distributions (SSDs). Interestingly, freshwater autotrophs are more sensitive to Irgarol than their marine counterparts. For marine autotrophs, microalgae are generally more sensitive to Irgarol than macroalgae and cyanobacteria. With very limited available data on M1 (i.e. five species), M1 might be less toxic than Irgarol; nonetheless this finding warrants further confirmation with additional data on other autotrophic species.     

Shell thickening in Crassostrea gigas: Organotin antifouling or sediment induced?

Crassostrea gigas spat were cultured for 8 weeks in the presence of a mixed algal diet in experimental tanks containing bis (tributyl tin) oxide (TBTO) alone, TBTO and a marine sediment, or a marine sediment alone. Growth measurements taken on a weekly basis showed enhanced weight gain in oysters exposed to nominal 50 and 100 mg l^?1 concentrations of marine sediment alone. Spat in low level TBTO treatments (0.15 μg l^?1) grew less well than the controls and showed pronounced thickening of the upper shell valve. High levels of TBTO (1.6 μg l^?1) severely inhibited oyster growth. Tissue concentrations of TBT compounds were measured at the end of the experiment. Bio-concentration factors of 3000- and 10000-fold were demonstrated for the high and low TBTO treatments respectively.     

Cenozoic evolution of the sulfur cycle: Insight from oxygen isotopes in marine sulfate

We report new data on oxygen isotopes in marine sulfate (δ¹⁸O_SO4), measured in marine barite (BaSO₄), over the Cenozoic. The δ¹⁸O_SO4 varies by 6‰ over the Cenozoic, with major peaks 3, 15, 30 and 55 Ma. The δ¹⁸O_SO4 does not co-vary with the δ³⁴S_SO4, emphasizing that different processes control the oxygen and sulfur isotopic composition of sulfate. This indicates that temporal changes in the δ¹⁸O_SO4 over the Cenozoic must reflect changes in the isotopic fractionation associated with the sulfide reoxidation pathway. This suggests that variations in the aerial extent of different types of organic-rich sediments may have a significant impact on the biogeochemical sulfur cycle and emphasizes that the sulfur cycle is less sensitive to net organic carbon burial than to changes in the conditions of that organic carbon burial. The δ¹⁸O_SO4 also does not co-vary with the δ¹⁸O measured in benthic foraminifera, emphasizing that oxygen isotopes in water and sulfate remain out of equilibrium over the lifetime of sulfate in the ocean. A simple box model was used to explore dynamics of the marine sulfur cycle with respect to both oxygen and sulfur isotopes over the Cenozoic. We interpret variability in the δ¹⁸O_SO4 to reflect changes in the aerial distribution of conditions within organic-rich sediments, from periods with more localized, organic-rich sediments, to periods with more diffuse organic carbon burial. While these changes may not impact the net organic carbon burial, they will greatly affect the way that sulfur is processed within organic-rich sediments, impacting the sulfide reoxidation pathway and thus the δ¹⁸O_SO4. Our qualitative interpretation of the record suggests that sulfate concentrations were probably lower earlier in the Cenozoic.     

Adsorption behaviour of dibutyl phthalate on marine sediments

Laboratory experiments were carried out to investigate the adsorption behaviour of dibutyl phthalate (DBP) on marine sediments collected from five different sites in Victoria Harbour, Hong Kong. DBP adsorption can be well described by the Langmuir isotherm. The maximum DBP adsorption capacity (Q_max) of the marine sediments ranges from 53 to 79 mg g⁻¹, which has a positive correlation with their organic content. Around 90% of the organic can be removed from the sediments with treatment by H₂O₂ oxidation, and the Q_max then decreases to a range between 13 and 22 mg g⁻¹. The black carbon content of the sediments has a much greater DBP adsorption capacity than does the natural organic matter of the sediments. The amount of DBP adsorbed on the sediments increases as the salinity of the marine water increases.     

Assessing the use of U–Th methods to determine the age of cold-water calcareous algae

Calcitic crusts of calcareous red algae could be suitable material for age determination of raised marine deposits and palaeothermometry at annual to sub-annual resolution. We examined the potential of U–Th dating of cold-water calcareous algae by analysing fossil specimens (n=10) from Kapp Ekholm (Svalbard) and recent specimens from Norway (n=3) and Scotland (n=1). After initial measurements using α-spectrometry, thermal ionisation mass spectrometry (TIMS) was used to study the material in more detail. Recent specimens contain 0.19–1.55 μg g⁻¹ U, and the measured (²³⁴U/²³⁸U) activity ratios vary between 1.12 and 1.30. Fossil specimens contain 1–168 μg g⁻¹ U, and display variable and highly elevated initial (²³⁴U/²³⁸U) activity ratios. In general, the TIMS results show increasing (²³⁴U/²³⁸U) activity ratios and concentrations of U and Th with increasing stratigraphic age. From this it is evident that marine calcareous red algae contain U in-vivo and they experience substantial post-mortem uptake of U. We conclude that direct U–Th dating of fossil calcareous algae from raised marine deposits is not viable without further geochemical understanding of the in-vivo uptake and post-depositional pathways of U and Th in such deposits. Despite the convincing open-system behaviour of the material, comparison with previously published chronostratigraphy from the site shows that the calcareous algae generally yield ages that are too old. This is in contrast to the expected result based on simple continuous post-mortem U accumulation and calls for a complex model comprising migration of U and multi-component addition of Th (detrital/colloidal) to explain the observed trends.     

Re-assessing the nitrogen signal in continental margin sediments: New insights from the high northern latitudes

Organic and inorganic nitrogen and their isotopic signatures were studied in continental margin sediments off Spitsbergen. We present evidence that land-derived inorganic nitrogen strongly dilutes the particulate organic signal in coastal and fjord settings and accounts for up to 70% of the total nitrogen content. Spatial heterogeneity in inorganic nitrogen along the coast is less likely to be influenced by clay mineral assemblages or various substrates than by the supply of terrestrial organic matter (TOM) within eroded soil material into selected fjords and onto the shelf. The δ¹⁵N signal of the inorganic nitrogen (δ¹⁵N_inorg) in sediments off Spitsbergen seems to be appropriate to trace TOM supply from various climate- and ecosystem zones and elucidates the dominant transport media of terrigenous sediments to the marine realm. Moreover, we postulate that with the study of sedimentary δ¹⁵N_inorg in the Atlantic–Arctic gateway, climatically induced changes in catchment's vegetations in high northern latitudes may be reconstructed. The δ¹⁵N_org signal is primarily controlled by the availability of nitrate in the dominating ocean current systems and the corresponding degree of utilization of the nitrate pool in the euphotic zone. Not only does this new approach allow for a detailed view into the nitrogen cycle for settings with purely primary-produced organic matter supply, it also provides new insights into both the deposition of marine and terrestrial nitrogen and its ecosystem response to (paleo-) climate changes.     

Terrestrial and marine biomarker estimates of organic matter sources and distributions in surface sediments from the East China Sea shelf

Revealing of the sources and distributions of sedimentary organic matter in the East China Sea (ECS) is important for understanding its carbon cycle, which has significant temporal and spatial variability due to the influences of recent climate changes and anthropogenic activities. In this study, we report the contents of both terrestrial and marine biomarkers including ∑C₂₇+C₂₉+C₃₁n-alkanes (38.6-580 ng/g), C₃₇ alkenones (5.6-124.6 ng/g), brassicasterol (98-913 ng/g) and dinosterol (125-1521 ng/g) from the surface sediments in the Changjiang River Estuary (CRE) and shelf areas of the ECS. Several indices based on biomarker contents and ratios are calculated to assess the spatial distributions of both terrestrial and marine organic matter in the ECS surface sediments, and these results are compared with organic matter distribution patterns revealed by the δ¹³C (−20.1‰ to −22.7‰) and C/N ratio (5-7.5) of total organic matter. The contents of terrestrial biomarkers in the ECS surface sediments decrease seaward, controlled mostly by Changjiang River (CR) inputs and surface currents; while higher contents of the two marine biomarkers (brassicasterol and dinosterol) occur in upwelling areas outside the CRE and in the Zhejiang-Fujian coastal zone, controlled mostly by marine productivity. Four proxies, f_Terr(δ¹³C) (the fraction of terrestrial organic matter in TOC estimated by TOC δ¹³C), odd-alkanes (∑C₂₇+C₂₉+C₃₁n-alkanes), 1/P_mar-aq ((C₂₃+C₂₅+C₂₉+C₃₁)/(C₂₃+C₂₅) n-alkanes) and TMBR (terrestrial and marine biomarker ratio) (C₂₇+C₂₉₊C₃₁n-alkanes)/((C₂₇+C₂₉+C₃₁) n-alkanes+(brassicasterol+dinosterol+alkenones)), reveal a consistent pattern showing the relative contribution of terrestrial organic matter (TOM) is higher in the CRE and along the Zhejiang-Fujian coastline, controlled mostly by CR inputs and currents, but the TOM contribution decreases seaward, as the influences of the CR discharge decrease.     

Organic sources and carbon sequestration in Holocene shelf sediments from the western Arctic Ocean

To quantify changes in organic carbon inputs and preservation, sediments from the Northern Chukchi Sea spanning the last 9000 years of the Holocene period were collected during the HOTRAX expedition and analyzed. The multi-proxy approach included molecular organic markers, bulk carbon and isotope measurements plus more recent approaches to terrestrial carbon estimation (the BIT index of Branched and Isoprenoid Tetraethers). The upper 1100 cm of the core, corresponding to the last 7.4 ka, showed a relatively stable total organic carbon content of 1.13-1.38% which decreased below 1100 cm to 0.6%. C:N ratios ranged from 8.4 to 10.83 over the Holocene time period examined. The distribution of n-alcohols and n-alkanes revealed major contributions from long-chain n-alcohols and n-alkanes while minimal contributions were seen from short-chain n-alkanes. The majority of the total fatty acids was comprised of saturated and monounsaturated fatty acids with short-chain and long-chain saturated fatty acids present in similar concentrations throughout most of the core and monounsaturated fatty acids decreasing down-core. Total sterol concentrations showed considerable inputs from marine sterols, C₂₈Δ^5,22, C₂₈Δ^5,24(28) and dinosterol, as well as C₂₉Δ⁵, typically considered a terrestrial marker. The BIT indices for core sediments ranged from 0.021 to 0.216 with minor changes seen in older sequences. Overall, organic biomarkers indicate marine sources as the more dominant input of organic matter with lower but continual contributions from terrestrial sources at this location during the Holocene. The remarkable consistency among multiple molecular organic markers of both marine and terrestrial origin over the Holocene period encompassed by the core suggests that sinking material or surface sediments were heavily influenced by bottom currents or other mixing processes prior to their deposition.     

Persistent organic pollutants in marine biota of São Pedro and São Paulo Archipelago,Brazil

Remote islands, such as the São Pedro and São Paulo Archipelago (SPSPA), Brazil, are pristine areas. However, these locations are not exempt from the arrival of anthropogenic agents, such as persistent organic pollutants (POPs). The present study aimed to determine the occurrence and distribution of POPs in the marine biota of the SPSPA. Sample extractions were performed using a microwave-assisted method. The predominant compounds were PCBs and DDTs, which respectively had mean wet weight concentrations of 62.23 and 9.23 ng g⁻¹ in the tropical two-wing flying fish (Exocoetus volitans), 78.66 and 6.81 ng g⁻¹ in the brown booby (Sula leucogaster) and 43.40 and 3.03 ng g⁻¹ in the red rock crab (Grapsus grapsus). Low levels of contaminants suggest a relative degree of isolation. Occurrence and distribution profiles of PCBs support long-range atmospheric transport as the main source of contamination and demonstrate the ubiquity of these pollutants in the marine environment.     

Stratigraphic gaps at northern South China Sea margin reflect changes in Pacific deepwater inflow at glacial Termination Ⅱ

To constrain short-term changes of climate and oceanography in the northern South China Sea(SCS)over interglacial marine isotope stage(MIS)5.5,we studied planktic and benthic 18O records of seven marine sediment cores with a time resolution of70–700 yr.Using 6–8 tie points the planktic records were tuned to the U/Th chronology of speleothem 18O records in China and Europe.The last occurrence of pink Globigerinoides ruber marks the top of Heinrich stadial 11(HS-11)near 128.4 ka.HS-11 matches a 2300-yr long positive 18O excursion by 1.5/0.8‰both in planktic and benthic 18O records.Hence half of the planktic 18O signal was linked to increased upwelling of18O-and12C-enriched deep waters in the southwestern SCS.The increase was possibly linked to a strengthened inflow of Pacific deep waters through the Bashi Strait,that form a boundary current along the northern slope of the SCS,building a major sediment drift.At its lower margin near 2300–2400 m water depth(w.d.)Parasound records reveal a belt of modern erosion.At the end of glacial termination 2,stratigraphic gaps deleted HS-11 in core MD05-2904 and subsequent peak MIS 5.5 at ODP Site 1144.Likewise hiatuses probably earmarked all preceding glacial terminations at Site 1144 back to 650 ka.Accordingly,boundary current erosion then shifted~300 m upslope to~2040–2060 m w.d.These vertical shifts imply a rise in boundary current buoyancy,that in turn may be linked to transient events of North Pacific deepwater formation similar to that traced in SCS and North Pacific paleoceanographic records over glacial termination 1.     

Source apportionment of sedimentary hydrocarbons in the Segara Anakan Nature Reserve,Indonesia

The study aimed to determine the spatial distribution of n-alkanes and polycyclic aromatic hydrocarbons (PAHs) in surface sediments of the Segara Anakan nature reserve and their potential origins using gas chromatography–mass spectrometry. Total alkane concentrations ranged from 3755 to 129,027 μg kg⁻¹, and the concentrations of 16 PAHs ranged from 375 to 29,517 μg kg⁻¹. The ratios of specific n-alkanes (e.g., CPI_24–34, WaxC_n, and Paq), including a new proposed index, terrestrial–marine discriminant (TMD), as well as the ratios of selected PAHs (e.g., Ant/∑178, Fl/∑202, BaAnt/∑228, and IPyr/∑276), showed that the sources of hydrocarbons in the sediments were generally biogenic, including both terrigenous and marine, with an anthropogenic pyrolytic contribution (petrogenic and biogenic combustion). For the environmental risk assessment, a sediment quality guideline (SQGs) comparison indicated that the station risk levels ranged from low to medium-low, except for R6, which has a greater impact on the ecological risk for marine organisms.     

Bioaccumulation of mercury in starfish from contaminated mussels

In the course of our works on mercury metabolism in marine organisms, we investigated in laboratory the technical feasibility and the scientific relevance of the simple benthic food chain ‘particles-mussel-starfish’. Mature starfish, Leptasterias polaris, fed over 45 days with contaminated mussels (Mytilus edulis), bioaccumulated organic mercury in all their tissues. The absorption rate of mercury in the first weeks of the experiment was respectively 0.238, 0.094, and 0.015 μg.g⁻¹ d⁻¹ (wet wt) in pyloric caeca, stomachs and body walls. Starfish retained about 50% of the organic mercury ingested mostly in pyloric caeca and calcerous skeleton (96–98%). After four weeks of regular accumulation, an auto-depuration process took place and mercury concentration in digestive organs was reduced even if the contaminated food was still provided. Coelomic fluid seems to be a barrier to the rapid dispersion of methylmercury into the whole animal and may play a role in the depuration process. These results provide evidence for the strong interest in the mussel-starfish food chain for fundamental studies of metal biotransfer in invertebrate marine organisms.