Numerous studies have shown that Steamboat Creek in Nevada is highly contaminated with mercury, with aqueous mercury concentrations more than two orders of magnitude greater than nearby mountain streams. One objective of this study was to determine if the new Spreadsheet-based Ecological Risk Assessment for the Fate of Mercury (SERAFM) model could be calibrated to the concentrations of unfiltered and dissolved total mercury, and unfiltered and dissolved MeHg in the water column for a reach on SBC and a related constructed wetland mesocosm for different seasons and residence times. SERAFM is a new U.S. Environmental Protection Agency steady state, single segment, mass balance mercury model that has been applied to lakes, and this study also examined the model’s applicability for modeling an arid flowing water environment in different seasons. The average combined error between observed and model-estimated mercury concentrations was 12% and 17% for the reach and mesocosm, respectively. Some recommendations are proposed that may allow SERAFM to better model flowing systems.

A 3-D biological model was developed and coupled to a hydrodynamic model, i.e., Princeton Ocean Model, to simulate the seasonal variation and budget of dissolved inorganic nitrogen, phosphate, and silicate in Jiaozhou Bay. The modeled nutrients distribution pattern is consistent with observation. Silicate, the most important limiting element for phytoplankton growth, is characterized by consumption in spring, increase in summer and autumn, and accumulation in winter, whereas dissolved inorganic nitrogen and phosphorous have increasing trend with low rates in spring, due to excessive river loads. Phytoplankton plays an important role in nutrient renewal by photosynthesis and respiration processes. During an annual cycle, 7.83 x 10³ t N, 0.28 x 10³ t P, and 3.93 x 10³ t Si are transported to the bay's outer sea, i.e., the Yellow Sea, suggesting that Jiaozhou Bay is a significant source of nutrients for the Yellow Sea. The spatial distribution of nutrients is characterized by vertically homogeneous profiles, with high concentration inside the bay and low concentration toward the bay channel. These features are mainly governed by strong turbulent mixing, fluvial influx, water exchange rate, and Yellow Sea water intrusion. Numerical experiments suggest that the government should pay enough attention to proper layout of sewage drainage.

The atmospheric deposition of reactive nitrogen on turf grassland in Tsukuba, central Japan, was investigated from July 2003 to December 2004. The target components were ammonium, nitrate, and nitrite ions for wet deposition and gaseous ammonia, nitric and nitrous acids, and particulate ammonium, nitrate, and nitrite for dry deposition. Organic nitrogen was also evaluated by subtracting the amount of inorganic nitrogen from total nitrogen. A wet-only sampler and filter holders were used to collect precipitation and the atmospheric components, respectively. An inferential method was applied to calculate the dry deposition velocity of gases and particles, which involved the effects of surface wetness and ammonia volatilization through stomata on the dry deposition velocity. The mean fraction of the monthly wet to total deposition was different among chemical species; 37, 77, and 1% for ammoniacal, nitrate-, and nitrite-nitrogen, respectively. The annual deposition of inorganic nitrogen in 2004 was 47 and 48 mmol m-² yr-¹ for wet and dry deposition, respectively; 51% of atmospheric deposition was contributed by dry deposition. The annual wet deposition in 2004 was 20, 27, and 0.07 mmol m-² yr-¹, and the annual dry deposition in 2004 was 35, 7.4, and 5.4 mmol m-² yr-¹ for ammoniacal, nitrate-, and nitrite-nitrogen, respectively. Ammoniacal nitrogen was the most important reactive nitrogen because of its remarkable contribution to both wet and dry deposition. The median ratio of the organic nitrogen concentration to total nitrogen was 9.8, 17, and 15% for precipitation, gases, and particles, respectively.

The health of near shore marine ecosystems has long been a concern because of its importance to coastal areas. Jiaozhou Bay (JZB) is one such marine ecosystem experiencing rapid water quality degradation in the last several decades. From the area surrounding the bay, the nutrients discharged into the bay through surface water and groundwater has been greatly changed. The thickness of the aquifers and the permeability is relatively high, the concentrations of nutrients in the groundwater are generally high, and so the groundwater discharged into JZB is very significant. However, no attempt has ever been made to evaluate the amount of nutrients discharged into the bay area via groundwater. In this study, the cross-section method and water balance method were used to estimate the amount of groundwater and nutrients discharged into JZB via the subsurface. Groundwater was monitored and sampled at aquifers surrounding the bay area, and some previously available data was also analyzed. The results indicated that groundwater from the Baisha Aquifer east of JZB now is the major source of nutrients (nitrate, dissolved SiO₂) being discharged into the bay. The concentrations of nutrients in the groundwater have been increasing with intensive agricultural land use. However, Dagu Aquifer, the largest aquifer north of JZB, only provides limited nutrients to the bay area because of the construction of a low permeability subsurface dam. Historically, during the 1970s to the 1990s, the Baisha Aquifer experienced seawater intrusion due to excessive groundwater withdrawal. The same was true for the Dagu Aquifer from the 1980s to the 1990s. Because of this, no significant nutrients were discharged into the bay.

Emissions of sulphur and oxidized nitrogen compounds in Europe have been reduced following a series of control measures during the last two decades. These changes have taken place during a period in which the primary gases and the wet deposition throughout Europe were extensively monitored. Since the end of the 1970s, for example land based sulphur emissions declined by between 90 and 70% depending on the region. Over the same period the total deposition of sulphur and its partitioning into wet and dry deposition have declined, but the spatial pattern in the reduction in deposition differs from that of emission and has changed with time. Such non-linearities in the emission-deposition relationship are important to understand as they complicate the process of assessing the effects of emission reduction strategies. Observed non-linearities in terrestrial sulphur emission-deposition patterns have been identified in north west Europe due to increases in marine emissions, and are currently slowing the recovery of freshwater ecosystems. Changes in the relative amounts of SO₂ and NH₃ in air over the last two decades have also changed the affinity of terrestrial surfaces for SO₂ and have therefore changed the deposition velocity of SO₂ over substantial areas. The consequence of this effect has been the very rapid reduction in ambient SO₂ concentration in some of the major source areas of Europe, where NH₃ did not change much. Interactions between the different pollutants, generating non-linearities are now being incorporated in long-range transport models to simulate the effects of historical emission trends and to provide projections into the future. This paper identifies non-linearities in emission deposition relationships for sulphur and nitrogen compounds in Europe using data from the EMEP long-rang transport model and measured concentration fields of the major ions in precipitation and of SO₂ and NO₂ in surface air.

A “multi-pollutant exposure programme” reflecting the new pollution situation where SO₂ is no longer the dominating pollutant has been performed by the International Co-operative Programme on Effects on Materials, including Historic and Cultural Monuments (ICP Materials) within the activities of the Convention on Long-range Transboundary Air Pollution. The main results obtained in the period 1997-2003 are summarised. Dose-response functions are presented for carbon steel, zinc, copper, bronze and limestone. Parameters involved in the functions include besides SO₂ and pH, which were included in the previously developed functions from ICP Materials, also the effect of particulate matter and HNO₃.

Mn biogeochemistry was studied from 1994 to 2003 in a small forested catchment in the central Czech Republic using the watershed mass balance approach together with measurements of internal stores and fluxes. Mn inputs in bulk deposition were relatively constant during a period of sharply decreasing acidic deposition, suggesting that the Mn source was terrestrial, and not from fossil fuel combustion. Mn inputs in bulk deposition and Mn supplied by weathering each averaged 13 mg m-² year-¹ (26 mg m-² year-¹ total input), whereas Mn export in streamwater and groundwater averaged 43 mg m-² year-¹. Thus an additional Mn source is needed to account for 17 mg m-² year-¹. Internal fluxes and pools of Mn were significantly greater than annual inputs and outputs. Throughfall Mn flux was 70 mg m-² year-¹, litterfall Mn flux was 103 mg m-² year-¹, and Mn net uptake by vegetation was 62 mg m-² year-¹. Large pools of labile or potentially labile Mn were present in biomass and surficial soil horizons. Small leakages from these large pools likely supply the additional Mn needed to close the watershed mass balance. This leakage may reflect an adjustment of the ecosystem to recent changes in atmospheric acidity.

Manganese (Mn) contamination of drinking water may cause aesthetic and human health problems when concentrations exceed 50 and 500 μg l⁻¹, respectively. In the UK, the majority of Mn-related drinking water supply failures originate from unpolluted upland catchments. The source of Mn is therefore soil, but the exact mechanisms by which it is mobilised into surface waters remain unknown. Elevated Mn concentrations in surface waters have been associated with the rewetting of dried upland soils and with conifer afforestation. We investigated these hypotheses in a laboratory experiment involving the drying and rewetting of intact soil cores (1,900 cm³ volume) of horizons of four representative soil type-land use combinations from an upland water supply catchment in southwest Scotland. Although no statistically significant effect of land use or soil type was detected on Mn concentrations in soil water, Mn release occurred from three soil horizons upon rewetting. Soil water Mn concentrations in the moorland histosol H2 (10–30 cm), the histic podzol H and Eh horizons increased from means of 5.8, 6.2 and 0.6 μg l⁻¹ prior to rewetting to maxima of 90, 76 and 174 μg l⁻¹ after rewetting, respectively. The properties of these three horizons indicate that Mn release is favoured from soil horizons containing a mixture of organic and mineral material. Mineral material provides a source of Mn, but relatively high soil organic matter content is required to facilitate mobilisation. The results can be used alongside soil information to identify catchments at risk of elevated Mn concentrations in water supplies.

Surface water is frequently contaminated by the trace metals, in particular lead and zinc, produced by mining activities. The infiltration of this water is likely to pollute surface soils and ground water. The study of the transfer of trace elements, especially lead, under real conditions is difficult to carry out due to the physicochemical and hydrodynamic complexity of real soil (preferential flows, conditions of unsaturation...), of the presence of colloids and of many candidate elements. The objective of the present study was to gain a better understanding of the parameters influencing the migration processes of trace elements in simplified systems; it was based on the study of Pb transfer in laboratory columns filled with soil. The results showed that retention of lead in soil is strongly dependent on feed flow rate, particulate bed tortuosity, bed height, water-soil surface contact and volume of water. Increase in bed height, water-soil surface contact and particulate bed tortuosity leads to higher contact time thus higher lead retention by soil, whereas increase in feed flow rate and volume of water leads to lower contact time thus lower lead retention by soil.

The prevalence and diversity of antibiotic resistant enterococci populations in samples collected four times from urban sewage treatment plant in Tehran, Iran between June 2005 and July 2006 were studied. Filtered samples were grown on mEnterococci medium containing 4 μg/ml vancomycin after which the enterococci isolates were identified to the species level. All strains were then tested for their resistance against nine antibiotics. Of the 131 isolates, 98 (75%) isolates were identified as Enterococcus gallinarum, followed by 24 (18%) and 9 (7%) for E. faecium and E. casseliflavus, respectively. All E. gallinarum isolates carried vanC1 gene with 64 (65%) and 14 (14%) isolates concomitantly harboured either vanA or vanB gene, respectively. Some E. casseliflavus concomitantly harboured vanA and vanC2 or vanB and vanC2. Typing the total enterococci isolates with a high resolution biochemical fingerprinting method showed a high diversity (D i = 0.91). We have shown by biochemical fingerprinting the presence of highly diverse glycopeptide resistant E. gallinarum and E. casseliflavus that have captured vanA and vanB genetic determinants under natural conditions. To our knowledge this is the first report in this geographical region showing high frequency antibiotic resistant enterococcal populations in particular E. gallinarum carrying assorted vancomycin resistance genes.