From 2000 to 2004, we sampled for total mercury (THg) and methylmercury (MeHg) in inlet streams to Lake Champlain, targeting high flow periods to capture increases in THg and MeHg concentrations with increasing flow. We used these data to model stream THg and MeHg fluxes for Water Years 2001 through 2009. In this mountainous forested basin with a high watershed-to-lake area ratio of 18, fluvial export from the terrestrial watershed was the dominant source of Hg to the lake. Unfiltered THg and MeHg fluxes were dominated by the particulate fraction; about 40% of stream THg was in the filtered (<0.4 μm) phase. THg flux from the watershed to the lake averaged 2.37 μg m⁻² yr⁻¹, or about 13% of atmospheric Hg wet and dry deposition to the basin. THg export from the lake represented only about 3% of atmospheric Hg input to the basin.

Lichens are an excellent model to study the bioaccumulation of heavy metals but limited information is available on the molecular mechanisms occurring during bioaccumulation. We investigated the changes of the lichen proteome during exposure to constant concentrations of mercury. We found that most of changes involves proteins of the photosynthetic pathway, such as the chloroplastic photosystem I reaction center subunit II, the oxygen-evolving protein and the chloroplastic ATP synthase β-subunit. This suggests that photosynthesis is a target of the toxic effects of mercury. These findings are also supported by changes in the content of photosynthetic pigments (chlorophyll a and b, and β-carotene). Alterations to the photosynthetic machinery also reflect on the structure of thylakoid membranes of algal cells. Response of lichens to mercury also involves stress-related proteins (such as Hsp70) but not cytoskeletal proteins. Results suggest that lichens adapt to mercury exposure by changing the metabolic production of energy.

Levoglucosan was present in all samples and its concentrations showed a pronounced annual cycle with maximum levels in the cold season. The annual percentage of ratios of levoglucosan to OC ranged from 0.04 to 9.75% evidencing a major contribution of biomass burning to the aerosol OC during the winter. In the urban-background site, OC was strongly correlated with EC in winter, suggesting that the major fraction of OC was generated as primary particles along with EC. A background levoglucosan component showed that biomass burning was continuously taking place in all the investigated sites. The biomass burning contribution to the Tuscany aerosol was made up of a background component and an additional component during winter probably due to wood burning for domestic heating.

The sensitivity of nitrifiers to crude oil released by the BP Deepwater Horizon oil spill in Gulf of Mexico was examined using characterized ammonia-oxidizing bacteria and archaea to develop a bioassay and to gain further insight into the ecological response of these two groups of microorganisms to marine oil spills. Inhibition of nitrite production was observed among all the tested ammonia-oxidizing organisms at 100ppb crude oil. Nitrosopumilus maritimus, a cultured representative of the abundant Marine Group I Archaea, showed 20% inhibition at 1 ppb, a much greater degree of sensitivity to petroleum than the tested ammonia-oxidizing and heterotrophic bacteria. The differing susceptibility may have ecological significance since a shift to bacterial dominance in response to an oil spill could potentially persist and alter trophic interactions influenced by availability of different nitrogen species.

In 2009 and 2010, 720 serum samples were collected from non-occupationally exposed study participants at four Korean locations and monitored for the presence of 27 polybrominated diphenyl ether (PBDE) congeners. The median concentrations of Σ₂₇PBDEs (the sum of 27 congeners) and Σ₃–₇PBDEs (the sum of tri- to hepta-BDE congeners) were 6.04 and 4.97 ng/g lipid, respectively. The most abundant congener detected in serum samples was BDE-153, followed by BDE-47 and BDE-99. The median value of Σ₃–₇PBDEs was similar to the median values observed in Asia and Europe, but much lower than that observed in North America. Some significant differences, based on geographic region and sex, were observed. We also observed a positive increase of BDE-153 with regard to age. In addition, we estimated the daily exposure to PBDEs from previously published reports of PBDE concentrations in food and dust, and determined the individual contributions of a variety of sources.

Triolein embedded cellulose acetate membrane (TECAM) passive samplers provide potentially powerful tool for monitoring time weighted average concentrations (CTWA) of trace hydrophobic organic contaminants in water. To study the field performance of TECAM, exchange kinetics of chemicals between water and TECAM were studied at different temperature and water flow rates. Results showed that the uptake rate constant (kᵤ) in TECAM was less sensitive to temperature variation than the SPMD and Chemcatcher. The kᵤ in TECAM was sensitive to even a slight change of the flow rate, which required the field calibration using performance reference compounds (PRCs). To estimate CTWA by TECAM, both empirical model and WBL model were compared in laboratory conditions, and only small differences were observed between the predicted and measured kᵤ. Field validation was conducted to test the sampler performance alongside spot sampling. A good agreement of water concentration was obtained by the two sampling techniques.

Ofloxacin (OFL) was used as a model antibiotic and the quenching of OFL fluorescence by DOM was examined with an emphasis on temperature-dependent quenching kinetics. OFL fluorescence intensity was corrected for inner filter and temperature effects. The kinetics data were fitted well using a two-compartment pseudo first-order kinetics model. Three quenching compartments were identified using this model, namely, a very fast quenching compartment (q₀) and two pseudo first-order quenching compartments (q₁ + q₂). The q₀ values had a positive relationship with temperature, while (q₁ + q₂) were negatively related with temperature. In addition, OFL–DOM binding quantified by (q₁ + q₂) was consistent with binding result obtained from dialysis equilibrium system. We concluded that q₀ was resulted from dynamic quenching, while (q₁ + q₂) was attributed to static quenching. The dynamic quenching of OFL by DOM accounted for 30–90% to the overall quenching and thus was very significant.

Knowledge of the partitioning and sources of mercury are important to understanding the human impact on mercury levels in Lake Superior wildlife. Fluvial fluxes of total mercury (HgT) and methylmercury (MeHg) were compared to discharge and partitioning trends in 20 sub-basins having contrasting land uses and geological substrates. The annual tributary yield was correlated with watershed characteristics and scaled up to estimate the basin-wide loading. Tributaries with clay sediments and agricultural land use had the largest daily yields with maxima observed near the peak in water discharge. Roughly 42% of HgT and 57% of MeHg was delivered in the colloidal phase. Tributary inputs, which are confined to near-shore zones of the lake, may be more important to the food-web than atmospheric sources. The annual basin-wide loading from tributaries was estimated to be 277 kg yr⁻¹ HgT and 3.4 kg yr⁻¹ MeHg (5.5 and 0.07 mg km⁻² d⁻¹, respectively).

Three beehive matrices, sampled in eighteen apiaries from West France, were analysed for the presence of lead (Pb). Samples were collected during four different periods in both 2008 and 2009. Honey was the matrix the least contaminated by Pb (min = 0.004 μg g⁻¹; max = 0.378 μg g⁻¹; mean = 0.047 μg g⁻¹; sd = 0.057). The contamination of bees (min = 0.001 μg g⁻¹; max = 1.869 μg g⁻¹; mean = 0.223 μg g⁻¹; sd = 0.217) and pollen (min = 0.004 μg g⁻¹; max = 0.798 μg g⁻¹; mean = 0.240 μg g⁻¹; sd = 0.200) showed similar levels and temporal variations but bees seemed to be more sensitive bringing out the peaks of Pb contamination. Apiaries in urban and hedgerow landscapes appeared more contaminated than apiaries in cultivated and island landscapes. Sampling period had a significant effect on Pb contamination with higher Pb concentrations determined in dry seasons.

Surface soils were collected in Balang Mountain to explore the environmental process of polychlorinated biphenyls (PCBs) and polybrominated diphenyl ethers (PBDEs) during air transport. The average concentrations of ∑₂₅PCBs and ∑₁₃PBDEs in soils were 163 pg/g and 26 pg/g, respectively. The significant correlations between the concentrations of pollutants and total organic carbon (TOC) indicated the importance of TOC in accumulation potential of POPs. The slopes from fitted curves of PCBs were highly related with logKₒₐ, demonstrating that TOC dominates the soil-air exchange of PCBs. The TOC-normalized concentrations of contaminants in samples from below-treeline were higher than those from alpine meadow, probably due to the forest filter effect. The increasing trends of the concentrations with altitude from the alpine meadow samples, could be attributed to the mountain cold-trapping effect. And the weak cold-trapping effect of POPs might be due to the less precipitation in 2008 when comparing with those in 2006.