Terry L. Wade

Enrichment of Heavy Metals and Organic Compounds in the Surface Microlayer of Narragansett Bay, Rhode Island

Concentrations of lead, iron, nickel, copper, fatty acids, hydrocarbons, and chlorinated hydrocarbons are enriched from 1.5 to 50 times in the top 100 to 150 micrometers of Narragansett Bay water relative to the bulk water 20 centimeters below the surface. Trace metal enrichment was observed in the particulate and organic fractions but not in the inorganic fraction. If these substances are concentrated in films only a few molecular layers thick on the water surface, the actual enrichment factor in the films may be well over 104, resulting in extremely high localized pollutant concentrations in the surface microlayer.

Historical contamination of PAHs, PCBs, DDTs, and heavy metals in Mississippi River Delta, Galveston Bay and Tampa Bay sediment cores

Profiles of trace contaminant concentrations in sediment columns can be a natural archive from which pollutant inputs into coastal areas can be reconstructed. Reconstruction of historical inputs of anthropogenic chemicals is important for improving management strategies and evaluating the success of recent pollution controls measures. Here we report a reconstruction of historical contamination into three coastal sites along the US Gulf Coast: Mississippi River Delta, Galveston Bay and Tampa Bay. Within the watersheds of these areas are extensive agricultural lands as well as more than 50% of the chemical and refinery capacity of the USA. Despite this pollution potential, relatively low concentrations of trace metals and trace organic contaminants were found in one core from each of the three sites. Concentrations and fluxes of most trace metals found in surface sediments at these three sites, when normalized to Al, are typical for uncontaminated Gulf Coast sediments. Hydrophobic trace organic contaminants that are anthropogenic (polycyclic aromatic hydrocarbons, DDTs, and polychlorinated biphenyls) are found in sediments from all locations. The presence in surface sediments from the Mississippi River Delta of low level trace contaminants such as DDTs, which were banned in the early 1970s, indicate that they are still washed out from cultivated soils. It appears that the DDTs profile in that sediment core was produced by a combination of erosion processes of riverine and other sedimentary deposits during floods. Most of the pollutant profiles indicate that present-day conditions have improved from the more contaminated conditions in the 1950-1970s, before the advent of the Clean Water Act.

NOAA gulf of Mexico status and trends program: Trace organic contaminant distribution in sediments and oysters

Polynuclear aromatic hydrocarbons (PAH), chlorinated pesticides, and polychlorinated biphenyls (PCB) concentrations were determined in sediment and oysters to provide information on the current status of the concentration of these contaminants in Gulf of Mexico coastal areas removed from point sources of input. Coprostanol analyses of sediments showed that anthropogenic materials are associated with the sediments at all 153 stations sampled. The levels of contaminants encountered are low compared with areas of known contamination. Average PAH concentrations are nearly the same in oysters and sediments, although the molecular weight distribution is different. Average DDT and PCB concentrations are higher by a factor of 10 to 130 in oysters as compared to sediments. Continued sampling and analyses will allow for long-term trends in the concentrations of these contaminants to be determined.

Status of persistent organic pollutants in the sediment from several estuaries in China

Sediment samples from three estuaries on the east coast of China were analyzed for persistent organic pollutants. Total PCB, PAH, and DDT concentrations in the sediments from Minjiang, Jiulongjiang, and Zhujiang estuaries ranged from 2 to 14 ng/g, 400 to 1500 ng/g, and 6 to 73 ng/g, respectively, in the sediments from these estuaries. The sources of PAH contamination were inferred from PAH compositions, with pyrogenic PAHs being the dominant source for Minjiang Estuary and petroleum related PAHs being the primary contributors to Jiulongjiang and Zhujiang estuaries. The high concentrations of DDT in the sediments from these estuaries were likely the result of widespread use of DDT in China in the 1960s and 1970s. Butyltin compounds were detected in the sediment from Jiulongjiang Estuary and Victoria Harbor, Hong Kong. Presence of butyltin compounds probably result from the shipping activities in these estuaries. Butyltin compounds were not detected in the sediments from Minjiang and Zhujiang estuaries. Contaminant concentrations were generally below levels expected to affect benthic organisms with the exception of DDTs.

Sediment contaminants in Casco Bay, Maine. Inventories, sources, and potential for biological impact

An inventory-based approach to environmental assessment that determines concentrations of sedimentary contaminants, defines their origins, and assesses the potential for biological impact is illustrated in Casco Bay, ME. The most widespread contaminants in Casco Bay are petroleum and petroleum byproducts. The highest concentrations of contaminants are associated with population centers, effluent outfalls, and spills. The majority of PAH in sediments are the product of high-temperature combustion processes. PAH concentrations at sites in close proximity to Portland exceed values believed to produce toxic responses in marine benthic organisms. In contrast, PCB, DDTs, and chlordane concentrations in the sediments are below concentrations thought to produce toxic effects in marine organisms. Metal concentrations in sediments are also below those that elicit biological responses. The geographic distribution of contaminants is initially controlled by the proximity to sources, and the regional differences in concentrations are the result of sediment accumulation patterns. Detrital (terrestrial), autochthonous marine, pyrogenic, and petroleum sources for PAH, alkanes, and trace metals are defined. 21 refs., 10 figs., 6 tabs.

Trace organic contamination in the Americas: An overview of the US National Status & Trends and the International ‘Mussel Watch’ programmes

Abstract The National Status & Trends (NS&T, 1986–1993) and the International Mussel Watch (IMW, 1991–1992) programmes provide a good coverage of a broad range of environmental conditions along the North, Central and South American coasts. Total concentrations of DDTs, chlordane-related compounds, PCBs and PAHs present fairly homogeneous distributions along the northern Gulf of Mexico coast, with very few sites showing extremely high or low concentrations. In contrast, a larger variability in the geographical distribution of some of these organic contaminants was observed for IMW sites. For example, high concentrations of DDT and its metabolites, DDD and DDE, were generally found in tropical and subtropical areas as compared to more temperate zones of South America. ‘Industrial’ contaminants, such as PCBs and PAHs, have similar distributions with the highest concentrations encountered generally along the southern South Atlantic coast. An overall comparison of the concentrations of these organic contaminants measured at NS&T and IMW sites indicates that contamination is significantly higher along the northern coast of the Gulf of Mexico.

Normalization of metal concentrations in estuarine sediments from the Gulf of Mexico

Metal concentrations were examined in sediments from 497 sites within the estuaries of the Gulf of Mexico by the United States Environmental Protection Agencys Environmental Monitoring and Assessment Program (EMAP). Data were normalized for extant concentrations of aluminum to isolate natural factors from anthropogenic ones. The normalization was based on the hypothesis that metal concentrations vary consistently with the concentration of aluminum, unless metals are of anthropogenic origin. Strong linear correlations (>75% variation explained) were observed between Al and Cr, Cu, Pb, Ni, and Zn. Moderate correlations (50–75% variation explained) were observed between Al and As or Ag. Weak but significant correlations (30–40% variation explained) were observed between Al and Hg or Cd. Based on these results, the spatial extent of contamination was examined. About 39% of sites with contamination by at least one metal occurred near population centers, industrial discharge sites, or military bases. The remainder of the observed contamination represented a dispersed pattern, including the lower Mississippi River (7%) and numerous agricultural watersheds (54%), suggesting that the contamination might be from nonpoint sources.

NOAA's status and trends mussel watch program: Chlorinated pesticides and PCBs in oysters (Crassostrea virginica) and sediments from the Gulf of Mexico, 1986–1987

Abstract Chlorinated pesticides and PCBs were analyzed in more than 590 oyster and sediment samples collected during 1986 and 1987, the first 2 years of the NOAAs Status and Trends Mussel Watch Program established to monitor the current status and temporal trends of these contaminants in the Gulf of Mexico. Chlorinated hydrocarbons in oysters and sediments presented similar distribution patterns; however, their concentrations in oysters were several times higher than the concentration detected in the surrounding sediments. Alpha-chlordane, trans -nonachlor and dieldrin were the most abundant non-DDT pesticides in both types of sample. The major fraction of DDT related compounds measured in oysters and sediments was DDD. Based on average PCB concentrations, penta-, hexa-, and tetrachlorobiphenyls were preferentially accumulated by oysters as compared to the average sediment composition. Although this study was designed to avoid known point-sources of contaminant inputs, the measured concentrations were, in general, within the range of concentrations previously reported for the Gulf of Mexico. After the first 2 years of this program, the geographical distribution of chlorinated hydrocarbons in oysters and sediments is well defined. In contrast, the temporal trends at the different sites are not clear. Continued sampling will allow the identification of long-term trends in concentrations of chlorinated hydrocarbons in the Gulf of Mexico.

Tributyltin contamination in bivalves from United States coastal estuaries.

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Human Contamination of the Marine Environment-Arthur Harbor and McMurdo Sound, Antarctica.

Polycyclic aromatic hydrocarbons (PAH), polychlorinated biphenyls (PCBs), pesticides, and trace metal concentrations in McMurdo Sound and Arthur Harbor, Antarctica, sediments and marine biota are reported. Biomarkers of contaminant exposure, biliary metabolites and EROD assays, were also measured. Hydrocarbon and trace metal contamination are generally limited to within hundreds of meters of human settlements. Local releases of fossil fuels, disposal of waste materials, and aging of ship and station structures contribute to contamination. High concentrations of PCBs were detected in sediments (250-4200 ng g{sup -1}) and organisms (up to 420 ng g{sup -1}) from Winter Quarters Bay (WQB). Trace metal and PAH sediment concentrations rarely exceed levels known to cause toxic effects in marine organisms, whereas PCBs in WQB often do. Biological responses to exposure include the formation of PAH metabolites and the inducement of the P4501A detoxification system in fish. Induction of EROD activity in in vitro rat hepatoma H4IIE cell bioassays by tissue extracts correlated with known levels of PCB contamination in invertebrate tissues. Local sources of contaminants greatly exceed those attributable to long-distance atmospheric transport. 31 refs., 4 figs.