Sedimentation and chronology of heavy metal pollution in Oslo harbor, Norway

Stratigraphic profiles of Cu, Cd and Hg in ten sediment cores from the Oslo harbor, Norway, combined with results of radiometric dating demonstrate that pollution by these metals peaked between 1940 and 1970. Dating results indicate that Hg discharges peaked between 1940 and 1950, Cd reached maximum ca. 1955-1960, and Cu has the highest concentration in sediment interval corresponding to ca. 1970. Geochemical profiles and maxima of Cu, Cd and Hg concentrations can be used as chronostratigraphic markers for sediment cores from the Oslo harbor. Acoustic backscatter and sediment core data indicate that propeller wash affects the seabed in the Oslo harbor. The propeller-induced turbulence causes erosion, and in places exposes and remobilizes contaminated sediments that accumulated in the harbor during previous decades. Such re-exposure of contaminated sediments could be detrimental to local ecosystems and offset remediation efforts, warranting further impact studies and potential mitigation strategies to prevent redistribution.     

Magnetic signature of hydrocarbon-contaminated soils and sediments at the former oil field H?nigsen, Germany

Magnetic properties of hydrocarbon (HC) containing soils and sediments from two sites (Site A and B) of the former oil-field H?nigsen were analyzed in order to determine whether magnetic methods can be employed to delineate HC contamination of soils and sediments. Magnetic parameters such as magnetic susceptibility and induced isothermal remanent magnetizations, as well as soil and sediment properties such as pH, iron content and water content, HC content and most probable number counts of iron-metabolizing microorganisms were determined. The magnetic concentration-dependent parameters for HC contaminated samples were 25 times higher in soils from Site A than in sediment samples from Site B. However, at Site B the magnetic susceptibility was still four times higher in comparison to lithologically similar non-contaminated sediment samples from a third Site C. Newly formed magnetite containing mainly single domain particles was responsible for the magnetic enhancement, whereas superparamagnetic grains represented only a minor component. Site A had an acidic pH compared to neutral pH at Site B, and a higher crystalline and bioavailable total iron content. Nevertheless, Site B samples contained significant numbers of both iron(II)-oxidizing and iron(III)-reducing microorganisms indicating that microbial iron cycling might have taken place at this site and potentially played a role for iron mineral transformation, including magnetite (trans)formation. The content of total non-polar hydrocarbons (TNPH) at Site A was one order of magnitude higher than at Site B. Only at Site A magnetic susceptibility correlated well with TNPH. Our results demonstrate that HC contaminated samples had an enhanced magnetite content compared to non-contaminated soils and sediments. Therefore, magnetic methods may provide a quick and cost-effective way to assess HC contamination in soils and sediments. However, more field sites and laboratory investigations are needed to reveal the complex nature of the processes involved.     

Environmental magnetic and petroleum hydrocarbons records in sediment cores from the north east coast of Tamilnadu, Bay of Bengal, India

In this study, mineral magnetic properties and petroleum hydrocarbons were statistically analysed in four sediment cores (C1, A1, T1 and K1) from the north east coast of Tamilnadu, India to examine the feasibility of PHC concentrations assessment using magnetic susceptibility. The C1 and A1 cores reveal a clear horizon of increase in PHC above 35 and 50 cm respectively suggesting the excess anthropogenic loading occurred in the recent past. Magnetic properties which were enhanced in the upper part of the sediment cores were the result of ferrimagnetic minerals from anthropogenic sources. Factor analysis confirmed that the input of magnetic minerals and petroleum hydrocarbons in Chennai coastal sediments are derived from the same sources. The present study shows that instead of expensive and destructive PHC chemical methods, magnetic susceptibility is found to be a suitable, cheap and rapid method for detailed study of petroleum hydrocarbon contamination in marine sediments.     

Studies of a contaminated brackish marsh in the Hackensack Meadowlands of northeastern New Jersey: an assessment of natural recovery

Eight-Day Swamp is known to be contaminated with heavy metals, especially mercury. Sediment cores were collected to approximately 32 cm at 17 sites on four transects and analyzed at 1 or 2 cm intervals for seven metals and organic matter. Very high metal levels were found throughout the site. Long and Morgan's "effects range-median" (ER-M) was exceeded in more than 50% of slices for all elements except As. Hg had the highest concentration relative to ER-M; median Hg concentration was 72 times its ER-M. On the marsh plain, all metals showed enrichment at 14-20 cm depth of 10-40X over surficial sediments. 137Cs analysis showed sedimentation rates ranging from 0.33 to 0.50 cm yr(-1) over the last approximately 40 yr. These rates indicate that metal contamination peaks occurred in sediments deposited in the early 1960s. Thus, newer, less contaminated sediments are burying older, more contaminated layers and peak levels of contaminants are becoming less available to benthos.     

Evidence that bio-metallic mineral precipitation enhances the complex conductivity response at a hydrocarbon contaminated site

The complex conductivity signatures of a hydrocarbon contaminated site, undergoing biodegradation, near Bemidji, Minnesota were investigated. This site is characterized by a biogeochemical process where iron reduction is coupled with the oxidation of hydrocarbon contaminants. The biogeochemical transformations have resulted in precipitation of different bio-metallic iron mineral precipitates such as magnetite, ferroan calcite, and siderite. Our main objective was to elucidate the major factors controlling the complex conductivity response at the site. We acquired laboratory complex conductivity measurements along four cores retrieved from the site in the frequency range between 0.001 and 1000 Hz. Our results show the following: (1) in general higher imaginary conductivity was observed for samples from contaminated locations compared to samples from the uncontaminated location, (2) the imaginary conductivity for samples contaminated with residual and free phase hydrocarbon (smear zone) was higher compared to samples with dissolved phase hydrocarbon, (3) vadose zone samples located above locations with free phase hydrocarbon show higher imaginary conductivity magnitude compared to vadose zone samples from the dissolved phase and uncontaminated locations, (4) the real conductivity was generally elevated for samples from the contaminated locations, but not as diagnostic to the presence of contamination as the imaginary conductivity; (5) for most of the contaminated samples the imaginary conductivity data show a well-defined peak between 0.001 and 0.01 Hz, and (6) sample locations exhibiting higher imaginary conductivity are concomitant with locations having higher magnetic susceptibility. Controlled experiments indicate that variations in electrolytic conductivity and water content across the site are unlikely to fully account for the higher imaginary conductivity observed within the smear zone of contaminated locations. Instead, using magnetite as an example of the bio-metallic minerals in the contaminated location at the site, we observe a clear increase in the imaginary conductivity response with increasing magnetite content. The presence of bio-metallic mineral phases (e.g., magnetite) within the contaminated location associated with hydrocarbon biodegradation may explain the high imaginary conductivity response. Thus, we postulate that the precipitation of bio-metallic minerals at hydrocarbon contaminated sites impacts their complex conductivity signatures and should be considered in the interpretation of complex conductivity data from oil contaminated sites undergoing intrinsic bioremediation.     

Preliminary study on the mineral magnetic properties of sediments from Kůlna Cave (Moravian Karst), Czech Republic

Summary Magnetic property variations in marine, lacustrine and loess-paleosol sequences have proved to be useful proxies in climate change studies. However in order to correctly interpret the record of the magnetic property variations it is absolutely necessary to have a good understanding of the cause of the observed variations. Most of the ambiguity in loess-paleosol studies is in distinguishing the role of pedogenesis from other climatic factors. Studying the mineral magnetic properties of the protected cave sediments which have not undergone pedogenesis allows us to determine the degree to which detrital input is climatically driven. These results will help us better understand the variations observed in the surficial loess-paleosol sequences. This study reports mineral magnetic data collected from entrance facies sediments deposited during the early Wurmian glacial stage in the Kůlna Cave. The entrance facies sediments consist of loess-like silts with varying amount of talus. The magnetic susceptibility record from these sediments shows higher values in layers originating in colder climates which is different to that commonly observed in surficial loess deposits. Higher values of magnetic susceptibility in Kůlna sediments are probably due to higher concentrations of ferromagnetic minerals (magnetite and maghemite) and due to an increased proportion of superparamagnetic grains. The magnetic mineralogy and the grainsize distribution (grains larger than superparamagnetic) appear not to change throughout the studied profiles. Higher magnetic susceptibility accompanied by an increase in the superparamagnetic fraction observed in the sediments deposited during colder periods can be explained by an increased input from a pedogenic source when the vegetation cover was reduced and the erosion rate increased.     

Geochemistry of the Springfield Plateau aquifer of the Ozark Plateaus Province in Arkansas,Kansas, Missouri and Oklahoma,USA

Geochemical data indicate that the Springfield Plateau aquifer, a carbonate aquifer of the Ozark Plateaus Province in central USA, has two distinct hydrochemical zones. Within each hydrochemical zone, water from springs is geochemically and isotopically different than water from wells. Geochemical data indicate that spring water generally interacts less with the surrounding rock and has a shorter residence time, probably as a result of flowing along discrete fractures and solution openings, than water from wells. Water type throughout most of the aquifer was calcium bicarbonate, indicating that carbonate‐rock dissolution is the primary geochemical process occurring in the aquifer. Concentrations of calcium, bicarbonate, dissolved oxygen and tritium indicate that most ground water in the aquifer recharged rapidly and is relatively young (less than 40 years). In general, field‐measured properties, concentrations of many chemical constituents, and calcite saturation indices were greater in samples from the northern part of the aquifer (hydrochemical zone A) than in samples from the southern part of the aquifer (hydrochemical zone B). Factors affecting differences in the geochemical composition of ground water between the two zones are difficult to identify, but could be related to differences in chert content and possibly primary porosity, solubility of the limestone, and amount and type of cementation between zone A than in zone B. In addition, specific conductance, pH, alkalinity, concentrations of many chemical constituents and calcite saturation indices were greater in samples from wells than in samples from springs in each hydrochemical zone. In contrast, concentrations of dissolved oxygen, nitrite plus nitrate, and chloride generally were greater in samples from springs than in samples from wells. Water from springs generally flows rapidly through large conduits with minimum water–rock interactions. Water from wells flow through small fractures, which restrict flow and increase water–rock interactions. As a result, springs tend to be more susceptible to surface contamination than wells. The results of this study have important implications for the geochemical and hydrogeological processes of similar carbonate aquifers in other geographical locations. Copyright © 2000 John Wiley & Sons, Ltd.     

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.     

PCBs in Central Vietnam coastal lagoons: levels and trends in dynamic environments

PCBs were analysed in surficial sediments and selected sediment cores collected between 2002 and 2008 in Central Vietnam coastal lagoons. The aim was to determine contamination levels and trends, and to evaluate the effects of anthropogenic pressures and natural events. Samples were mostly fine-grained with low total PCB concentrations (0.367-44.7 μg kg⁻¹). Atmospheric transport and post depositional processes modify to some degree the fingerprint of PCB inputs to the environment favouring the predominance of 3, 4 and 5 chlorinated congeners. The similarity of congener distributions in contemporary surficial samples also suggests the presence of a unique source over the entire study area, probably connected to mobilisation and long range transports from land-based stocks. The removal of consistent sediment layers is hypothesised based on repeated samplings of the same area. Natural meteorological events (such as typhoons) are suspected to be responsible for these sediment losses.     

Metals in marine sediments near a large California municipal outfall

Elevated concentrations of trace metals in surficial sediments off Palos Verdes Peninsula, site of the Los Angeles County outfall system, clearly reflect the submarine discharge of treated municipal (domestic and industrial) wastewater. The following contamination factors (median outfall/median baseline) were obtained for the eight metals measured in a 45 km² region of the outfall monitoring zone: Ag-27; Cd-36; Cr-12; Cu-20; Hg-23; Ni-5.4; Pb-17; Zn-7.7.     

Magnetic characteristics of sediment grains concurrently contaminated with TBT and metals near a shipyard in Busan,Korea

Bottom sediments near shipyards are often susceptible to receiving accidental spills of TBT and metals or their degradation products from hull scraping of antifouling system paints applied prior to 2008, when the AFS Convention 2001 was not in force. We investigated TBT and metal contamination of sediments near the shipyards of a small marina located in Busan, Korea and found that they were highly contaminated with TBT, Cu, and Zn. To better understand the environmental impacts and to make an optimal remediation plan, we characterized individual antifouling fragments in terms of metal and TBT contents, magnetic properties, and grain-size. Coarse-sized individual antifouling fragments exhibited simultaneously high levels of TBT, metals and high magnetic susceptibility, and appeared to be a major source of pollution in the sediment. Therefore, magnetic separation in combination with size-separation appears to be a cost-effective remediation method to remove the TBT and metals from contaminated shipyard sediments.     

The distribution of heavy metals including Pb,Cd and Cr in Kendari Bay surficial sediments

The surficial coastal sediments in Kendari Bay are sampled in the field to determine the concentration and pollution level of three heavy metals (Pb, Cd and Cr). Twenty-five sampling points ranging from the inner (Wanggu River) to the outer area of the bay have been chosen. The physicochemical properties, such as temperature, pH, salinity and TDS of the overlying water, as well as the sediment type and TOC of the surficial sediments, are also measured. The total concentrations of the Pb, Cd and Cr in the sediment samples are quantified using inductively-coupled plasma mass spectrometry (ICP-MS). The concentrations of the heavy metals (Pb, Cd and Cr) ranged from 0.84 to 17.02 μg/g, 0.02 to 0.17 μg/g and 1.92 to 40.11 μg/g (dry weight), respectively, following the Cr > Pb > Cd sequence. To assess the degree of contamination, a geoaccumulation index (I_geo) is measured. Kendari Bay is not a contaminated area regarding Pb, Cd and Cr.     

Nearshore sediment pollution in Israel by trace metals derived from sewage effluent

Sediments along the Israeli coast were examined to determine the effects of large scale dumping of sewage on trace metal contents. The Tel Aviv-Yafo sewage pipeline outlet is the largest point source of sewage effluent along the coast.Significant quantities of trace metals—Ag, Co, Cr, Cu, Hg, Ni, Pb and Zn—were found in sediments extending to a distance as far as 400 m from the sewage pipeline outlet. Beyond this point, sufficient dilution occurs to limit contamination by sewage to relatively low levels at present. In the contaminated area, there are seasonable variations with maximum trace metal concentrations occurring in the summer. The upper layers of the cores contain a greater trace metal burden than do the lower.     

Gas chromatographic analyses of Argo Merchant oil and sediment hydrocarbons at the wreck site

Hydrocarbon concentrations were determined in surface sediments in the vicinity of the Argo Merchant wreck site. Of the 4000 km² area surveyed, contaminated sediments were found in a 10–15 km² section around the wreck site in February 1977. The contamination was in the form of small tar particles (or oil droplets) inhomogeneously mixed into the sandy sediments by the turbulent shoal tidal currents. Although there was no clear trend of hydrocarbon concentrations as a function of depth, contamination extended at least to 8–13 cm in depth. Stations which were contaminated in February were reoccupied on a cruise in July 1977. Only one station showed any trace of hydrocarbon contamination and this level was significantly lower than found at this site in February.     

Tracing anthropogenic contamination in the Pearl River estuarine and marine environment of South China Sea using sterols and other organic molecular markers

5beta-Coprostanol together with eight other sterols and unresolved complex mixtures (UCMs) were quantitatively investigated for surficial sediments and surface waters to assess the impacts of anthropogenic activities on the Pearl River estuarine and marine environment of South China Sea. The studied area extends from the Pearl River Estuary southward to the open sea. 5beta-Coprostanol concentrations ranged from trace amounts to 53 microgg(-1) TOC in surficial sediments. The highest levels and highest percentages of coprostanol were found in the Pearl River estuary, especially in the inner estuary and those sites close to the submarine outfalls of Hong Kong. For waters, only in estuarine samples was coprostanol quantitatively detected, ranging from 11 to 299 ngL(-1). Bimodal UCM "humps" were observed for most sediment samples, with concentrations ranging from 215 to 10,491 microg g(-1) TOC in sediments and from 2 to 26 mcirogL(-1) in waters, respectively. Progressive seaward declines in concentrations were found for both 5beta-coprostanol and UCM in surficial sediments. Trace or no 5beta-coprostanol was found in open-sea samples. Concentrations of coprostanol and UCM in surficial sediments are correlated. These results imply that there are obvious anthropogenic contaminations in the Pearl River estuary. The submarine outfalls in Hong Kong represent important sources of the sewage pollution to the Pearl River estuarine sediments evidenced by a combination of coprostanol concentration, diagnostic indices, sterol profiles and UCM. No obvious dispersion or transport of the sewage contamination occurred from the Pearl River estuary to the open South China Sea indicated by fecal sterol biomarkers.     

埃及Faiyum盆地沉积物中粒度和磁化率对风沙活动的指示意义

埃及Faiyum盆地是尼罗河下游的泛滥平原,沉积物主要来自尼罗河和撒哈拉沙漠.本文通过对钻孔FYAM(孔深4.6m)沉积物的粒度、磁化率的分析,并结合石英形态、石膏和碳酸盐含量分析,旨在寻找Faiyum盆地沉积物中代表风沙活动的粒度、磁化率特征.研究结果显示,钻孔沉积物中共发现7种粒度频率曲线类型,主要为细粒组(6-2...     

Distribution and characteristics of PAHs in sediments from the Mediterranean coastal environment of Egypt

To assess the contamination of polycyclic aromatic hydrocarbons (PAHs) in the Mediterranean coastal environment of Egypt, 26 sediment samples from the coastline, harbours, estuaries and coastal lakes were collected and analyzed. The sediment PAH concentrations of thirty-nine 2-6 ring PAHs ranged from 13.5 to 22,600 ng/g. PAH profiles varied according to the nature of the site and its proximity to sources. Industrialized and urbanized region showed high level of PAHs contamination. In general, the contamination levels of PAHs were similar to those observed in contaminated and slightly contaminated sediments of the Mediterranean Sea. Molecular indices based on ratios of selected PAH concentrations were used to differentiate PAHs from pyrogenic and petrogenic and mixed origins. Good correlations were observed between the petrogenic index, MP/P, A-PAHs/P-PAHs and HMW/LMW. Finally, PAH levels in sediments were compared with Sediments Quality Guidelines (ERM-ERL) for evaluation of probable toxic effects on organism.     

Chemical contamination of a coral reef by the grounding of a cruise ship in Bermuda

Bulk metal analyses of surficial sediments collected around the Norwegian Crown cruise ship grounding site in Bermuda indicated significant but localized contamination of reef sediments by copper and zinc, caused by the stripping of the tri-butyltin (TBT)-free antifouling (AF) paint (Intersmooth 460) from the underside of the hull. Highest copper and zinc values were found in heavily compacted and red-pigmented sediments inside the impact scar and were comparable to levels found close to slip ways of local boat yards where AF paints from hull stripping and cleaning processes are washed into the sea. The re-distribution of AF contaminated sediments by storms and deposition on nearby reefs constitutes a significant ecological risk that could delay recovery processes and reduce the effectiveness of remediation efforts. Whilst the ecotoxicological effects of AF paint particles interspersed with sediment is unknown, and in need of further study, it is argued that the significance of AF paint contamination of grounding sites has been overlooked.     

Contamination of polychlorinated biphenyls (PCBs) in sediments from Kyeonggi Bay and nearby areas, Korea

To elucidate the characteristic distribution and contamination of polychlorinated biphenyls (PCBs) in sediments, 63 sediments and five benthic organisms from Kyeonggi Bay, Namyang Bay and Lake Shihwa, West coast of Korea, were analysed. Characterization of PCBs distribution in sediments was conducted by correlation between PCBs concentrations and environmental parameters, comparison of contamination level and composition of PCBs homologs between Kanechlor mixture (KC-mix) and sediments. The residues of PCBs in sediments were correlated with total organic carbon (TOC) and particulate organic carbon (POC) contents, not with mud contents and grain size distributions. Elevated concentrations of T-PCBs were found in sediments from Incheon North Harbor (INH) in Kyeonggi Bay. T-PCBs concentrations were decreased with distance increase from inner site of INH. The residues of T-PCBs in sediments from Namyang Bay were either non-detectable or near to detection limit. The contamination by PCBs in sediments from Lake Shihwa was also low. The PCBs congener profiles in INH were similar to those of KC-mix, while those in less contaminated sites showed relatively high percentage of lower chlorinated biphenyls. Sites K18 (580 ng/g or 48 ug/g-OC dry wt) and K19 (330 ng/g or 38 ug/g-OC dry wt) within INH exceeded the sediment quality criteria (SQC) (16 micrograms/g-OC as a KC-mix) derived from equilibrium partitioning (EqP) approach.     

Concentrations of PCBs in coastal mangrove sediments of Hong Kong

The concentrations of polychlorinated biphenyls (PCBs) in surface sediments of ten mangrove sites in Hong Kong were determined by Congener-specific and Arcolor methods. Spatial variations were found between mangrove sites and within the same site, indicating that the sediment samples were heterogeneous and total PCBs concentrations in mangrove sediments should be normalised to compensate for natural variability and for identifying serious anthropogenic contamination. In addition to total organic carbon, Al, Fe and Mn were possible normalisers. Based on PCB/normaliser ratio and 95% prediction limits of scatter plots between total PCB and normaliser, all mangrove sites were not seriously contaminated by human activities. The estimated total PCBs concentrations (quantified by Congener-specific method) for most sediment ranged from 0.5 to 5.8 ng g(-1) (dry weight, n = 92). However, very high concentrations of PCB were found in sub-samples from Yi O, Tolo Pond and Lai Chi Wo, suggesting that these samples represented the PCB contaminated "hot spots".