Baseline metal concentrations in coastal Labrador sediments

Levels of Cr, Cu, Fe, Pb, Ni, and Zn in surface sediment from the Voisey's Bay area of coastal Labrador showed no evidence of recent anthropogenic input of metals. Metal concentrations in surface sediments, normalized to Li, fell within the 95% confidence limits of the background levels. Further analysis showed that the Li-metal regression lines from the surface sediments and sediments from 30-cm depth had the same slope and intercepts, suggesting that there was no difference in the metal content of the sediments at the two depths. Li-metal relationships can be used as a measure of the natural variability of the metal concentrations for the region and will serve as a baseline against which future anthropogenic affects may be assessed.     

Assessment of heavy metal contamination in the surficial sediments from the lower Meghna River estuary,Noakhali coast,Bangladesh

Sediment samples were collected from ten selected sites of the lower Meghna River estuary,and six heavy metals were analyzed with Atomic Absorption Spectrophotometry(AAS)to assess the contamination level and the metals’association with sediment grain size.The current results revealed that the mean concentrations of the studied metals were ranked in descending order of iron(Fe)(1.29×103 mg/kg)>zinc(Zn)(42.41 mg/kg)>lead(Pb)(12.48 mg/kg)>chromium(Cr)(10.59 mg/kg)>copper(Cu)(6.22 mg/kg)>cadmium(Cd)(0.28 mg/kg).The geo-accumulation,contamination,and pollution load indexes suggested that the lower Meghna river estuary was not contaminated by Fe,Zn,Pb,Cr,and Cu.The mean size of the sediment ranged from 28.92 to 126.2 mm,and the Pearson correlation coefficient showed a significant association between Fe and Pb(coefficient of determination,r2=0.836;p<0.05),and no significant correlation was found between individual metals and grain size,indicating no or low influence on the metals distribution.     

Metal concentrations, fluxes, inventories and chronologies in sediments from Sepetiba and Ribeira Bays: A comparative study

Three sediment cores were sampled at Sepetiba Bay and four cores at Ribeira Bay, Rio de Janeiro State, Brazil. Sediment accumulation rates and chronologies were obtained from ²¹⁰Pb activity-depth profiles. Sediment accumulation rates in Ribera Bay ranged from 1.2 mm y⁻¹ in the inner bay to 2.6 mm y⁻¹ close to its entrance. In Sepetiba Bay two sediment accumulation rates were observed: a lower rate of 0.35 cm y⁻¹ before the 1960s and 0.76 cm y⁻¹ since then. The cause of this change is due to the construction of the Santa Cecília impoundment (1955) that brings water from the Paraíba do Sul Basin into the Guandu River, which increased its flow from the original 20 m³ s⁻¹ to 160 m³ s⁻¹. Concentration of 44 elements was obtained by ICP-MS after total dissolution of samples from two selected cores. The relative differences between the concentrations of crustal elements, such as Al, Fe and Ti are only about 20% (p < 0.05). Cd and Zn are 15 and four times larger in Sepetiba Bay than in Ribeira Bay, respectively. Other major and minor elements show lower statistically significant differences. The enrichment factors and metal inventories show that Sepetiba Bay can be considered polluted with Bi, Cd, Cr, Cu, Sb and Zn. Particularly, Cd and Zn present concentrations three and four times higher than the Brazilian existing limits.     

MELIMEX,an experimental heavy metal pollution study: Regulation of trace metal concentrations in limno-corrals

In three limno-corrals of the MELIMEX project the transport paths of the trace metals Cu, Zn, Cd, Hg and Pb and the reaction of the systems on increased metal loads were investigated. The metal balances lead to the conclusion that the biomass is the main factor responsible for the regulation of trace metal concentration. The observed sequence of relative residence times of the trace metals can be described with a steady-state model. Additional metal load decreases the ability of the limnic system to lower the metal concentration. The production of phytoplankton and its assimilation capacity for metals are reduced leading to relatively higher metal concentrations in the lake.     

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.     

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.     

The initial assessment of trace metal pollution in coastal sediments

Coastal sediments are important hosts for pollutant trace metals, but analytical difficulties can prevent them being included in routine environmental monitoring programmes. In order to identify a suitable approach to the problem, an established simple technique has been evaluated for the initial assessment of trace metal pollution in coastal sediments. The technique, which involves leaching the samples with cold 0.5 N HCl, has been applied to surface sediments from two Greek gulfs and has been shown to provide a rapid, inexpensive way of initially establishing the gross degree to which a sediment population has been subjected to trace metal pollution from the overlying waters.     

A biomonitoring study: Heavy metals in macroalgae from eastern Aegean coastal areas

The concentrations of metals were measured in macroalgae species seasonally at eight coastal stations along the eastern Aegean coast. Sediment and seawater samples were also collected to detect their metal contents in order to gain more information on the environmental conditions of the area and possible bioaccumulation patterns. The aim of this study is, to gather more information on the use of selected species as cosmopolitan biomonitors for the eastern Aegean; to provide information on the marine environmental quality by the use of macroalgae and to determine which algae species are suitable as biomonitoring species for the study area. The relative abundance of metals in macroalgae decreases in the order: Fe-Zn-Cu-Cr-Cd-Hg-Pb and seawater: Fe-Zn-Pb-Cu-Cr-Cd-Hg. In sediment the distribution order from higher to lower was Fe-Cr-Zn-Pb-Cu-Hg-Cd. The brown algae Cystoseira sp., the green algae Ulva sp. and Enteromorpha sp. possess high potential as cosmopolitan biomonitors for trace metals in the Aegean Sea.     

Noble gas isotopic abundances and noble metal concentrations in sediments from the Cretaceous-Tertiary boundary

Noble gases in four sediment samples from the Cretaceous-Tertiary boundary collected near Stevns in Denmark were investigated to test the possibility of the presence of noble gases indicative for meteorites. All samples were also analyzed for the noble metals Os and Ir and twelve other elements. The observed enrichments of³He,⁴He and of Ar, Kr, and Xe relative to atmospheric abundances can be explained without invoking the addition of extraterrestrial material. The ²⁰Ne/²²Ne ratio and the Kr and Xe isotopic compositions are identical with the isotopic ratios in the terrestrial atmosphere. In contrast, the high noble metal concentrations indicate the presence of material with elemental abundances similar to chondritic matter. Compared to noble metals the noble gases are less sensitive tracers of an admixture of extraterrestrial matter in sediments.     

Chemical forms of heavy metal contaminants in sediments of Miyun reservoir

The chemical forms, spatial distribution and sources of As, Hg, Cd, Pb and Zn in sediments of the Miyun reservoir were studied. The results of sequential extraction demonstrate that most of As, Pb and Zn were bound to the residual fraction, Hg was associated with the sulfide fraction while Cd was associated with the carbonate fraction and the residual fraction. On the vertical profiles the concentrations of the heavy metals in total and each fractions mostly decreased with increasing depths in sediments, suggesting that the heavy metals input from the upstream watershed increases yearly. Summation of the residual fraction, the sulfide fraction and the carbonate fraction accounts for 60.03%―85.60% of the total heavy metal contents in the sediments, which represent the geochemical background values of the elements and relate closely to soil erosion. Results of the main factor analysis show that most sediments of the reservoir come from the upstream soil erosion, the point source pollution and domestic waste. Moreover, the microbial activities taking place on the sediment-water interface are also one of the major factors to cause the increasing content of the organic matter fraction and the iron-manganese oxide fraction. Environmental change of the reservoir water could make the removability of the heavy metals increase, leading to the increase of their concentrations in pore water in sediments, and imperiling water quality of the reservoir.