Trace metal concentrations and fluxes in Bermuda sediments

Concentrations and calculated fluxes of trace metals into Bermuda nearshore marine and lake sediments are presented. In areas affected by anthropogenic activity, metal profiles show surface sediment enrichments similar to those observed in North American and European lacustrine and estuarine sediments. Atmospheric fluxes of Cu, Zn and Pb into the lake sediments are higher than those of rural areas in North America. These high fluxes are assumed to be due to jet-fuel combustion. Sediment profiles in the Hamilton City area indicate increased anthropogenic input of Cu and Pb compared to other marine locations.     

Distribution and enrichment evaluation of heavy metals in Mejillones Bay (23°S), Northern Chile: Geochemical and statistical approach

A suite of 36 surface sediment samples, taken between 10 and 100 m water depth in Mejillones Bay (Northern Chile), were analyzed for mineralogy, grain size, total organic carbon, Al, and heavy metal content (Cd, Zn, Ni, Mn, V, Mo). Quartz and feldspars were the main lithogenic minerals and carbonate the predominant biogenic mineral. Sediments were fine sands in the shallow zone and organic silt in the deeper zone.

Enrichment Factor and Factor Analysis approach showed that the presence of Mn in the marine sediment of Mejillones is due to a partial influence of continental input, while all other metals are not supported by lithogenic debris. Although all metals showed high concentrations in the marine sediment of Mejillones Bay, comparison between metal concentration in surface sediments and preindustrial levels in this bay, show that present values agree with natural levels.     

Sources and transport of As,Cu, Cd and Pb in the environmental compartments of Deception Island,Antarctica

Sources and transport processes of As, Cu, Cd and Pb were studied in different environmental compartments of Deception Island, an active volcano in the South Shetland Islands, Antarctica. Element concentrations in fresh water samples are consistent with the lowest values reported elsewhere in Antarctica. Interestingly, higher concentration values of As were found in samples collected in or near spring water courses and its transport may be related with processes of lixiviation in underground waters. While in saline waters Cu and Pb had important punctual sources, concentration values for Cd were consistently high pointing to the existence of a natural and diffuse source possibly related with the hydrothermal activity. The high Si/Al ratio, low carbon content, and a non-significant anthropogenic heavy metal input may explain the surprisingly homogeneous heavy metal content found in sediment samples.     

Distribution and enrichment evaluation of heavy metals in Mejillones Bay (23 degrees S), Northern Chile: geochemical and statistical approach

A suite of 36 surface sediment samples, taken between 10 and 100 m water depth in Mejillones Bay (Northern Chile), were analyzed for mineralogy, grain size, total organic carbon, Al, and heavy metal content (Cd, Zn, Ni, Mn, V, Mo). Quartz and feldspars were the main lithogenic minerals and carbonate the predominant biogenic mineral. Sediments were fine sands in the shallow zone and organic silt in the deeper zone. Enrichment Factor and Factor Analysis approach showed that the presence of Mn in the marine sediment of Mejillones is due to a partial influence of continental input, while all other metals are not supported by lithogenic debris. Although all metals showed high concentrations in the marine sediment of Mejillones Bay, comparison between metal concentration in surface sediments and preindustrial levels in this bay, show that present values agree with natural levels.     

Distribution and accumulation of heavy metals in carbonate and reducible fractions of marine sediment from offshore mid-western Taiwan

Two marine sediment cores from offshore mid-western Taiwan were subsampled and pre-treated using a sequential extraction procedure to separate carbonate and reducible fractions. Aliquots of these extracts were analyzed to determine their chemical composition to evaluate the geochemical processes responsible for heavy metal distribution and accumulation in the coastal environment. Our data demonstrate that sedimentation rates derived from excess ²¹⁰Pb associated with metal fluxes show large increases circa A.D. 1990. A well-synchronized increase in metal flux in both geochemical fractions was found and validated by Pearson’s correlation. Principal component analysis revealed the heavy metal fluxes to be highly correlated with the sediment deposition rate, with metal contamination potentially driven by a sole contributor. This study emphasizes the changes in sedimentation rate is potentially caused by activities associated with the inland economic development during this time, rather than by raising heavy metal pollution dominated the accumulation offshore mid-western Taiwan.     

The Estuarine Quality Paradox, Environmental Homeostasis and the difficulty of detecting anthropogenic stress in naturally stressed areas

Estuaries have long been regarded as environmentally naturally stressed areas because of the high degree of variability in their physico-chemical characteristics, for example oxygen, temperature and salinity in the water column and bed sediment dynamics. However, their biota is well-adapted to cope with that stress and so the areas may be regarded as resilient because of that inherent variability; their ability to absorb stress without adverse effects is regarded here as Environmental Homeostasis. Hence these areas may only be regarded as stressful for marine or freshwater-adapted organisms and that for estuarine organisms this environmental stress is regarded as a subsidy whereby they successfully capitalise on the stressful conditions. In addition, using examples of the estuarine fauna and flora, this article indicates that the characteristics of natural stress in estuaries are similar to those for anthropogenic stress. An over-reliance on ecosystem structural features, such as diversity, in quality indicators therefore makes the detection of the anthropogenic stress more difficult. This difficulty is termed the Estuarine Quality Paradox. Because of these difficulties, the article argues that functional characteristics either as well as or rather than structural ones should be used in detecting environmental perturbations in estuaries.     

Crustacean assemblages in a polluted estuary from South-Western Spain

The spatial-temporal variation in crustacean assemblages of the Odiel-Tinto estuary, one of the most polluted areas in the world, was studied in 2000, 2002 and 2004. The crustacean assemblages were mainly established according to the natural gradient from estuarine to marine environment (based on water and sediment characteristics such as dissolved oxygen, salinity, granulometry or organic content). Pollutants such as copper, zinc or phosphates could also explain partially this pattern based on BIOENV and canonical correspondence analyses. However, there were clear symptoms of perturbation, mainly in the inner areas, such as a low number of species and a low abundance, especially in relation to the typical estuarine species (e.g. Cyathura carinata, Corophium spp.). This study provides baseline information which can be used as a reference point in a long-term perspective.     

Mercury-water interactions in the estuarine environment

Examination of mercury-water interactions in the estuarine environment reveals that, while locally mercury concentration in estuarine waters may reflect external influence on the estuarine system, the interactions of the heavy metal with soluble and insoluble water components greatly influence the transport of the metal and its impact on the biota in natural waters. In connection with transformation of mercury in aquatic ecosystems, the role played by methylation in spatial and temporal mobilization of mercury is viewed in wider perspective. This throws light on metal concentration and dispersion and the need for monitoring them in any realistic environmental management design.     

Sediment geochemistry of the urban Lake Paulo Gorski

The objective of this study was to evaluate the concentration and distribution of heavy metals in the sediments of Paulo Gorski Lake, as well as the metals’ bioavailability and potential ecological risk, and to define the anthropogenic and natural heavy metal contributions to the lake. The chemical elements calcium (Ca), cadmium (Cd), cobalt (Co), chromium (Cr), copper (Cu), iron (Fe), potassium (K), magnesium (Mg), manganese (Mn), sodium (Na), nickel (Ni), lead (Pb), and zinc (Zn) were quantified by flame atomic absorption spectrophotometry with two extraction methods to quantify the bioavailable and non-bioavailable fractions. The data were evaluated using multivariate statistics and sediment quality indices. All sediment collection points (S1, S2, S3, S4 and S5) are different in terms of the concentration of heavy metals, except for S4 and S5, which were statistically equal. The bioavailable fraction of the elements in the sediment follows the sequence Pb>Cu>Mn>Zn>Ni>Cr>phosphorus (P) for all points. The elements Co, Cr, Pb, and Zn showed moderate to considerable contamination at all points. Only points S3 and S5 had moderate ecological risk. Urbanization has been affecting Paulo Gorski Lake via the input of chemical elements, especially Co and Pb. The points most affected by heavy metal contamination are S3 and S5 when the sedimentological sensitivity factor is considered. The lake has high hydrodynamics, causing some of the contaminants that enter the system to leave it, leading to potential negative impacts downstream.     

Heavy metal contamination in coastal sediments and soils near the Brazilian Antarctic Station, King George Island

This paper investigates the natural and anthropogenic processes controlling sediment chemistry in Admiralty Bay, King George Island, Antarctica, emphasizing the area affected by the Brazilian Antarctic Station Comandante Ferraz (Ferraz). Total and bioavailable concentrations of sixteen elements were determined in 32 sediment and 14 soils samples. Factor analysis allowed us to distinguish three groups of samples: (1) Ferraz sediments, with higher content of total trace metals and organic matter; (2) control sediments, with intermediate characteristics; (3) Ferraz soils, with higher bioavailability of most metals due to its oxidizing condition and low organic matter content. Major elements such as Fe, Al, Ca and Ti presented similar levels in all three groups. Enrichment factor calculations showed that paints, sewage and petroleum contamination enhanced metal concentrations in Ferraz surface sediments as follows: B, Mo, and Pb (>90%); V and Zn (70-80%); Ni, Cu, Mg, and Mn (30-40%). Despite evidence of contamination in these sediments, the low bioavailability, probably caused by iron-sulfide, indicates small environmental risks.     

Plastic ‘scrubbers’ in hand cleansers: a further (and minor) source for marine pollution identified

Small, inconspicuous fragments of plastic, generally < 0.5 mm across (i.e. microlitter) derived from some hand cleaners and cosmetic preparations, and also used with some airblast cleaning media, are an unusual addition to post-consumer waste entering marine waters. The environmental significance of this material is unknown, but here is a further example of the intrusion of anthropogenic waste of dubious value into marine ecosystems. It could impact sea-surface microlayer ecosystems and the meiofauna of intertidal sediments. It is also speculated that these finely granulated plastics, once dispersed through the oceanic water column, could prejudice the results of some ambitious particulate carbon flux experiments as well as interfere with elemental and mineralogic composition analyses of suspended particles. They may also warrant attention when determining heavy metal concentrations in contaminated fine-grained sediments of estuarine and harbour environments.     

Comprehensive assessment of heavy metal contamination in sediment of the Pearl River Estuary and adjacent shelf

Total metal concentrations (Cr, Ni, Cu, Zn, and Pb), acid volatile sulfide and simultaneously extracted metals (AVS-SEM), and heavy metal fractionation were used to assess the heavy metals contamination status and ecological risk in the sediments of the Pearl River Estuary (PRE) and adjacent shelf. Elevated concentrations at estuarine sites and lower concentrations at adjacent shelf sites are observed, especially for Cu and Zn. Within the PRE, the concentration of heavy metals in the western shore was mostly higher than that in the middle shore. The metals from anthropogenic sources mainly occur in the labile fraction and may be taken up by organisms as the environmental parameters change. A combination of total metal concentrations, metal contamination index and sequential extraction analysis is necessary to get the comprehensive information on the baseline, anthropogenic discharge and bioavailability of heavy metals.     

Spatial budgetary evaluation of organochlorine contaminants in the sediments of Cochin Estuary,India

This paper presents the first detailed investigation on the residual levels of organochlorine insecticide (OCI) concentrations in the Cochin estuarine sediment. It aims in elucidate their distribution and ecological impact on the aquatic system. Concentrations of persistent organochlorine compound (OC) were determined for 17 surface sediment samples which were collected from specific sites of Cochin Estuarine System (CES) over a period of November 2009 and November 2011. The contaminant levels in the CES were compared with other worldwide ecosystems. The sites bearing high concentration of organochlorine compounds are well associated with the complexities and low energy environment. Evaluation of ecotoxicological factors suggests that adverse biological effects are expected in certain areas of CES.     

Geoaccumulation and distribution of heavy metals in the urban river sediment

Current study presents the application of chemometric techniques to comprehend the interrelations among sediment variables whilst identifying the possible pollution source at Langat River,Malaysia.Surface sediment samples（0-10 cm）were collected at 22 sampling stations and analyzed for total metals（~（48）Cd,~（29）Cu,~（30）Zn,~（82）Pb）,pH,redox potential（Eh）,salinity,electrical conductivity（EC）,loss on ignition（LOI）and cation exchange capacity（CEC）.The principal component analysis（PCA）scrutinized the origin of environmental pollution by various anthropogenic and natural activities：four principal components were obtained with 86.34%（5 cm）and88.34%（10 cm）.Standard,forward and backward stepwise discriminant analysis effectively discriminate 2variables（84.06%）indicating high variation of heavy metals accumulation at both depth.The cluster analysis accounted for high input of Zn and Pb at LA8,LA 10,LA 11 and LA 12 that mergers three（5 cm）and four（10cm）into clusters.This is consistent with the contamination factor（C_1）that shows high Cd（LA 1）and Pb（LA 7,LA 8,LA 10,LA 11 and LA 12）contaminations at 5cm.These indicate that Pb and Zn are the most bioavailable metals in the sediment with significant positive linear relationship at both sediment depths.Therefore,this approach is a good indication of environmental pollution status that transfers new findings on the assessment of heavy metals by interpreting large complex datasets and predicting the fate of heavy metals in the sediment.     

Potentially Bioavailable Natural Organic Carbon and Hydrolyzable Amino Acids in Aquifer Sediments

This study evaluated the relationship between concentrations of operationally defined potentially bioavailable organic ‐carbon (PBOC) and hydrolyzable amino acids (HAAs) in sediments collected from a diverse range of chloroethene‐‐contaminated sites. Concentrations of PBOC and HAA were measured using aquifer sediment samples collected at six selected study sites. Average concentrations of total HAA and PBOC ranged from 1.96 ± 1.53 to 20.1 ± 25.6 mg/kg and 4.72 ± 0.72 to 443 ± 65.4 mg/kg, respectively. Results demonstrated a statistically significant positive relationship between concentrations of PBOC and total HAA present in the aquifer sediment (p < 0.05). Higher levels of HAA were consistently observed at sites with greater levels of PBOC and first‐order decay rates. Because amino acids are known to be readily biodegradable carbon compounds, this relationship suggests that the sequential chemical extraction procedure used to measure PBOC is a useful indicator of bioavailable carbon in aquifer sediments. This, in turn, is consistent with the interpretation that PBOC measurements can be used for estimating the amount of natural organic carbon available for driving the reductive dechlorination of chloroethenes in groundwater systems.     

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.     

Levels of Cd,Cu, Pb and V in marine sediments in the vicinity of the Single Buoy Moorings (SBM3) at Mina Al Fahal in the Sultanate of Oman

Recently in the Sultanate of Oman, there has been a rapid surge of coastal developments. These developments cause metal contamination, which may affect the habitats and communities at and near the coastal region. As a result, a study was conducted to assess the level of metal contamination and its impact on the marine sediments in the vicinity of the Single Buoy Moorings 3 (SBM3) at Mina Al Fahal in the Sultanate of Oman. Marine subtidal sediment samples were collected from six different stations of the SBM3 for the period ranging from June 2009 to April 2010. These samples were then analyzed for their level and distribution of the heavy metals of cadmium (Cd), copper (Cu), lead (Pb) and vanadium (V). Overall, low concentrations of all four heavy metals were measured from the marine sediments, indicating that the marine at SBM3 is of good quality.     

Dynamic behaviour of polycyclic aromatic hydrocarbons in Brighton marina, UK

The distribution of polycyclic aromatic hydrocarbons (PAHs) between various phases is fundamental in the control of their movement and impact in the marine environment. In this study samples of water and sediments were regularly collected from Brighton marina, UK, to quantify the intensity, spatial and temporal variations of PAH contamination. The results show clearly that PAH behaviour in marine systems is highly complex, and controlled by the interplay of PAH sources, compound physicochemical properties, water and sediment movement, and field conditions. Levels of total PAHs (16 compounds) in the dissolved phase were found to vary between <2 and 11,400 ng/l, with higher values observed in the winter months. Total PAH concentration in sediment samples varied between 24 and 4710 ng/g dry weight. PAHs in water were dominated by low molecular mass compounds (2-ring), while PAHs in sediments were mainly derived from 2-4 ring compounds. In addition, dissolved concentrations were increased during sediment dredging and after a period of severe rainfall. PAHs in Brighton marina are likely to be from both pyrolytic and petrogenic sources; as a result, field-derived distribution coefficients for individual PAHs between sediment and water tend to follow the equilibrium partition models, although slight exceedance is apparent. The extended partition model incorporating soot carbon has achieved limited success in better predicting PAH behaviour.     

Behaviour of hexachlorocyclohexane isomers and Zn,Cu and Cd in the freshwater-seawater mixing area

Dissolved and suspended concentrations of hexachlorocyclohexane isomers, α, γ and δ HCH, and Zn, Cu and Cd have been measured in the Napostá Grande stream, located in the Blance Bay area, Argentina, for the purpose of studying the behaviour of these compounds in the freshwater-seawater mixing zone. The aim was to establish the mobilization processes, according to their distribution over the dissolved and suspended forms, in order to obtain a better understanding of their impact on organochlorine and heavy metal levels in the marine environment. It is concluded that the compounds studied are removed from solution by suspended matter which is afterwards precipitated during the freshwater-seawater mixing process. Seawater and surface sediment concentrations of these pollutants for two sampling sites in Blanca Bay, Argentina, are also reported.     

Heavy metal content and lithological properties of recent sediments in the Northern Adriatic

Heavy metal (Hg, Pb, Cd, Cu, Cr, Ni, Co, Zn and Fe) concentrations, textural characters and mineralogical compositions have been determined on 246 surface sediment samples from the Northern Adriatic Italian sea area. The relationship between the heavy metals content and the pelite (< 63 μm fraction) percentage has been studied. All the metals resulted accumulated in the fine fraction with the following percentages (Hg, 95%; Zn, 86%; Pb, 82%; Cu, 79%; Cd, 74%; Ni, 70%; Cr, 65%; Co, 65% and Fe, 64%). The specific surface area has been measured on 44 samples and correlated to metal values. A fairly good (50% and more variation explained) linear correlation co-efficient has been found for Ni and Cu in the entire area, less significant correlation for other metals. In order to discriminate between natural and anthropogenic origin the metal concentrations on the whole sediment has been normalized on the basis of the pelite percentage. In the areal distributions drawn with the corrected values, zones contaminated by industrial discharges have been identified mainly in front of the lagoon of Venice.