Rhizosphere soil and dominant plant samples were collected at a brownfield site in New Jersey, USA, during summer 2005 to evaluate plant metal uptake from the contaminated soils. Metal concentrations varied from 4.25 to 978 μg g⁻¹ for As, 9.68–209 μg g⁻¹ for Cr, 23.9–1870 μg g⁻¹ for Cu, and 24.8–6502 μg g⁻¹ for Zn. A wide range of metal uptake efficiencies in the roots, stems and leaves was found in this study. Data showed that (1) Betula populifolia has high Zn, Cu and As accumulations in the root, and high concentrations of Cu and Zn in the stem and the leaf; (2) Rhus copallinum has high accumulation of Zn and Cr in the leaf and Cu in the stem; (3) Polygonum cuspidatum has high accumulations of Cu and As in the root; and (4) Artemisia vulgaris shows high Cu accumulation in the leaf and the stem.

Blue crabs from a contaminated estuary (Hackensack Meadowlands-HM) and a cleaner reference site (Tuckerton-TK) were analyzed for Cr, Cu, Hg, Pb, and Zn in muscle and hepatopancreas. Crabs from each site were taken into the laboratory and fed food from the other site, or in another experiment, transplanted to the other site for eight weeks. All crabs were analyzed for metals. Overall, tissue concentrations reflected environmental conditions. Tissue differences were found for Cu, Pb and Zn (all higher in hepatopancreas), and Hg (higher in muscle). HM muscle had more Hg than TK muscle, but did not decrease after transplanting or consuming clean food. HM crabs lost Cu, Pb and Zn in hepatopancreas after being fed clean food or transplanted. TK crabs increased Hg in muscle and Cr and Zn in hepatopancreas after transplantation or being fed contaminated (HM) food. Concentrations were variable, suggesting that blue crabs may not be fully reliable bioindicators of polluted systems. The accumulation of metals within the muscle and hepatopancreas of blue crabs was highly variable, but often followed environmental concentrations.

Organohalogen pollutants are of concern in many river and estuarine environments, such as the New York-New Jersey Harbor estuary and its tributaries. The Hackensack River is contaminated with various metals, hydrocarbons and halogenated organics, including polychlorinated biphenyls (PCBs) and polychlorinated dibenzo-p-dioxins. In order to examine the potential for microbial reductive dechlorination by indigenous microorganisms, sediment samples were collected from five different estuarine locations along the Hackensack River. Hexachlorobenzene (HCB), hexabromobenzene (HBB), and pentachloroaniline (PCA) were selected as model organohalogen pollutants to assess anaerobic dehalogenating potential. Dechlorinating activity of HCB and PCA was observed in sediment microcosms for all sampling sites. HCB was dechlorinated via pentachlorobenzene (PeCB) and trichlorobenzene (TriCB) to dichlorobenzene (DCB). PCA was dechlorinated via tetrachloroaniline (TeCA), trichloroanilines (TriCA), and dichloroanilines (DCA) to monochloroaniline (MCA). No HBB debromination was observed over 12 months of incubation. However, with HCB as a co-substrate slow HBB debromination was observed with production of tetrabromobenzene (TeBB) and tribromobenzene (TriBB). Chloroflexi specific 16S rRNA gene PCR-DGGE followed by sequence analysis detected Dehalococcoides species in sediments of the freshwater location, but not in the estuarine site. Analysis targeting 12 putative reductive dehalogenase (rdh) genes showed that these were enriched concomitant with HCB or PCA dechlorination in freshwater sediment microcosms.

Sediment and polyethylene sampler-based estimates of polychlorinated dibenzo-p-dioxin/dibenzofuran (PCDD/F) concentrations in Newark Bay, New Jersey (USA) benthic biota were compared. Biota concentrations based on sediment were estimated using an organic carbon (OC)-water partitioning model and an OC and black carbon (BC)-water dual model. Biota concentrations based on polyethylene were estimated from samplers deployed in the Newark Bay water column and samplers immersed in a sediment/porewater slurry in the laboratory. Porewater samplers provided the best estimates of biota concentrations (within 3.1×), with best results achieved for deposit-feeders (within 1.6×). Polyethylene deployed in deep water also provided good estimates of biota concentrations (within 4×). By contrast, OC-water partitioning overestimated biota concentrations by up to 7×, while OC and BC combined underestimated biota concentrations by up to 13×. We recommend passive samplers such as polyethylene for estimating concentrations of hydrophobic organic contaminants in field biota given its simplicity and relatively lower uncertainty compared to sediment equilibrium partitioning.

Polychlorinated biphenyls (PCBs) were measured in the air and water over the Hudson River Estuary during six intensive field campaigns from December 1999 to April 2001. Over-water gas-phase PCB concentrations averaged 1100 pg/m3 and varied with temperature. Dissolved-phase PCB concentrations averaged 1100 pg/L and displayed no seasonal trend. Uncertainty analysis of the results suggests that PCBs with 5 or fewer chlorines exhibited net volatilization. The direction of net air/water exchange could not be determined for PCBs with 6 or more chlorines. Instantaneous net fluxes of PCBs ranged from +0.2 to +630 ng m-2 d-1. Annual fluxes of [summation operator]PCBs were predicted from modeled gas-phase concentrations, measured dissolved-phase concentrations, daily surface water temperatures and wind speeds. The net volatilization flux was +62 μg m-2 yr-1, corresponding to an annual loss of +28 kg/yr of PCBs from the Hudson River Estuary for the year of 2000. Investigation of the air-water exchange of PCBs in the Hudson River Estuary suggests that PCBs with 5 or fewer chlorines undergo net volatilization.

Sediment samples from the coastal lagoons and estuaries of New York and New Jersey were used to investigate the influence of contaminants on diatom assemblages. Multivariate analyses demonstrated correspondence between composition of diatom assemblages and concentrations of several metals and total PAH. The effects of the individual contaminants were difficult to disentangle because of the considerable correlations between their concentrations. The most conspicuous trend was the increase in the relative abundance of small centric planktonic diatoms in response to contamination and the corresponding decrease in the benthic flora. The high relative abundance of planktonic species on contaminated sediments apparently resulted not so much from their tolerance to pollution, but from the paucity of benthic species. A comparison of the assemblages on the surface and at the depth of approximately 8–10cm revealed a statistically significant temporal change in community composition towards planktonic diatoms.

Resident mussels are effective indicators of ecosystem health and have been utilized in national assessment and monitoring studies for over two decades. Mussels were chosen because contaminant concentrations in their tissues respond to changes in ambient environmental levels, accumulation occurs with little metabolic transformation and a substantial amount of historic data were available. Mussels were collected from 10 previously studied locations approximately a year after Hurricane Sandy. Regionally, concentrations of polychlorinated biphenyls (PCBs) and polycyclic aromatic hydrocarbons (PAHs) decreased significantly, while concentrations of organochlorine pesticides (OCPs) remained unchanged, and polybrominated diphenyl ethers (PBDEs) increased compared to historic concentrations. Although concentrations of PCBs, OCPs and PAHs were at or near record low concentrations, long-term trends did not change after Hurricane Sandy. To effectively measure storm-induced impacts it is necessary to understand the factors influencing changes in mussel body burdens and have a long-term monitoring network and an ability to mobilize post event.

Bed sediment samples from 79 coastal New York and New Jersey, USA sites were analyzed for 75 compounds including wastewater associated contaminants, PAHs, and other organic compounds to assess the post-Hurricane Sandy distribution of organic contaminants among six regions. These results provide the first assessment of wastewater compounds, hormones, and PAHs in bed sediment for this region. Concentrations of most wastewater contaminants and PAHs were highest in the most developed region (Upper Harbor/Newark Bay, UHNB) and reflected the wastewater inputs to this area. Although the lack of pre-Hurricane Sandy data for most of these compounds make it impossible to assess the effect of the storm on wastewater contaminant concentrations, PAH concentrations in the UHNB region reflect pre-Hurricane Sandy conditions in this region. Lower hormone concentrations than predicted by the total organic carbon relation occurred in UHNB samples, suggesting that hormones are being degraded in the UHNB region.

Hurricane Sandy made landfall in Barnegat Bay, October, 29, 2012, damaging shorelines and infrastructure. Estuarine sediment chemistry and toxicity were investigated before and after to evaluate potential environmental health impacts and to establish post-event baseline sediment-quality conditions. Trace element concentrations increased throughout Barnegat Bay up to two orders of magnitude, especially north of Barnegat Inlet, consistent with northward redistribution of silt. Loss of organic compounds, clay, and organic carbon is consistent with sediment winnowing and transport through the inlets and sediment transport modeling results. The number of sites exceeding sediment quality guidance levels for trace elements tripled post-Sandy. Sediment toxicity post-Sandy was mostly unaffected relative to pre-Sandy conditions, but at the site with the greatest relative increase for trace elements, survival rate of the test amphipod decreased (indicating degradation). This study would not have been possible without comprehensive baseline data enabling the evaluation of storm-derived changes in sediment quality.

Mercury (Hg) is considered a contaminant of global concern for coastal environments due to its toxicity, widespread occurrence in sediment, and bioaccumulation in tissue. Coastal New Jersey, USA, is characterized by shallow bays and wetlands that provide critical habitat for wildlife but share space with expanding urban landscapes. This study was designed as an assessment of the magnitude and distribution of Hg in coastal New Jersey sediments and critical species using publicly available data to highlight potential data gaps. Mercury concentrations in estuary sediments can exceed 2μg/g and correlate with concentrations of other metals. Based on existing data, the concentrations of Hg in mussels in southern New Jersey are comparable to those observed in other urbanized Atlantic Coast estuaries. Lack of methylmercury data for sediments, other media, and tissues are data gaps needing to be filled for a clearer understanding of the impacts of Hg inputs to the ecosystem.