Effectiveness of Emission Controls to Reduce the Atmospheric Concentrations of Mercury.

Coal-fired power plants in the United States are required to reduce their emissions of mercury (Hg) into the atmosphere to lower the exposure of Hg to humans. The effectiveness of power-plant emission controls on the atmospheric concentrations of Hg in the United States is largely unknown because there are few long-term high-quality atmospheric Hg data sets. Here, we present the atmospheric concentrations of Hg and sulfur dioxide (SO2) measured from 2006 to 2015 at a relatively pristine location in western Maryland that is several (>50 km) kilometers downwind of power plants in Ohio, Pennsylvania, and West Virginia. Annual average atmospheric concentrations of gaseous oxidized mercury (GOM), SO2, fine particulate mercury (PBM2.5), and gaseous elemental mercury (GEM) declined by 75%, 75%, 43%, and 13%, respectively, and were strongly correlated with power-plant Hg emissions from the upwind states. These results provide compelling evidence that reductions in Hg emissions from power plants in the United States had their intended impact to reduce regional Hg pollution.

Dry deposition of gaseous oxidized mercury in Western Maryland.

The purpose of this study was to directly measure the dry deposition of gaseous oxidized mercury (GOM) in western Maryland. Annual estimates were made using passive ion-exchange surrogate surfaces and a resistance model. Surrogate surfaces were deployed for seventeen weekly sampling periods between September 2009 and October 2010. Dry deposition rates from surrogate surfaces ranged from 80 to 1512 pgm(-2)h(-1). GOM dry deposition rates were strongly correlated (r(2)=0.75) with the weekly average atmospheric GOM concentrations, which ranged from 2.3 to 34.1 pgm(-3). Dry deposition of GOM could be predicted from the ambient air concentrations of GOM using this equation: GOM dry deposition (pgm(-2)h(-1))=43.2 × GOM concentration-80.3. Dry deposition velocities computed using GOM concentrations and surrogate surface GOM dry deposition rates, ranged from 0.2 to 1.7 cms(-1). Modeled dry deposition rates were highly correlated (r(2)=0.80) with surrogate surface dry deposition rates. Using the overall weekly average surrogate surface dry deposition rate (369 ± 340 pg m(-2)h(-1)), we estimated an annual GOM dry deposition rate of 3.2 µg m(-2)year(-1). Using the resistance model, we estimated an annual GOM dry deposition rate of 3.5 µg m(-2)year(-1). Our annual GOM dry deposition rates were similar to the dry deposition (3.3 µg m(-2)h(-1)) of gaseous elemental mercury (GEM) at our site. In addition, annual GOM dry deposition was approximately 1/2 of the average annual wet deposition of total mercury (7.7 ± 1.9 µg m(-2)year(-1)) at our site. Total annual mercury deposition from dry deposition of GOM and GEM and wet deposition was approximately 14.4 µg m(-2)year(-1), which was similar to the average annual litterfall deposition (15 ± 2.1 µg m(-2)year(-1)) of mercury, which was also measured at our site.

Estimation of ambient PM2.5 concentrations in Maryland and verification by measured values.

In 1997, Maryland had no available ambient Federal Reference Method data on particulate matter less than 2.5 microm in aerodynamic diameter (PM23), but did have annual ambient data for PM smaller than 10 microm (PM10) at 24 sites. The PM10 data were analyzed in conjunction with local annual and seasonal zip-code-level emission inventories and with speciated PM2.5 data from four nearby monitors in the IMPROVE network (located in the national parks, wildlife refuges, and wilderness areas) in an effort to estimate annual average and seasonal high PM2.5 concentrations at the 24 PM10 monitor sites operating from 1992 to 1996. All seasonal high concentrations were estimated to be below the 24-hr PM2.5 National Ambient Air Quality Standards (NAAQS) at the sites operating in Maryland between 1992 and 1996. The estimates also indicated that 12 monitor sites might exceed the 3-year annual average PM2.5 NAAQS of 15 microg/m3, but Maryland's air quality shows signs that it has been improving since 1992. The estimates also were compared with actual measurements after the PM2.5 monitor network was installed. The estimates were adequate for describing the chemical composition of the PM2.5, forecasting compliance status with the 24-hr and annual standards, and determining the spatial variations in PM2.5 across central Maryland.

Poultry litter ash as a potential phosphorus source for agricultural crops.

Maryland will impose restrictions on poultry litter application to soils with excessive P by the year 2005. Alternative uses for poultry litter are being considered, including burning as a fuel to generate electricity. The resulting ash contains high levels of total P, but the availability for crop uptake has not been reported. Our objective was to compare the effectiveness of poultry litter ash (PLA) and potassium phosphate (KP) as a P source for wheat (Triticum aestivum L.) in acidic soils, without and with limestone application. Two acidic soils (pH 4.25 and 4.48) were studied, unlimed or limed to pH 6.5 before cropping. The PLA and KP were applied at 0, 39, and 78 kg P ha(-1), after which wheat was grown. Limestone significantly increased wheat yield, but the P sources without limestone did not. The two P sources were not significantly different as P fertilizer. At the 78 kg P ha(-1) rate, wheat shoot-P concentrations were 1.10 and 1.12 g kg(-1) for the PLA treatment compared with 0.90 and 0.89 g kg(-1) for KP in the nonlimed and limed soils, respectively. Trace element concentrations in wheat shoots from the PLA treatment were less than or equal to KP and the control. The low levels of water-soluble P and metals in the soils and the low metal concentrations in wheat suggest that PLA is an effective P fertilizer. Further studies are needed to determine the optimum application rate of PLA as a P fertilizer.

Comparison of fine particles and the relationship between particle variations and meteorology at an urban site and a remote site in the Eastern United States.

This study compared the variations in the mass of certain particles at an urban site, Washington, DC, and at a remote site, Shenandoah National Park, VA, in the eastern United States. Seven years (1991-1997) of Interagency Monitoring of Protected Visual Environments (IMPROVE) fine particulate matter (PM2.5), PM10, coarse fraction, SO4(2-), and total sulfur data were used for this study together with available meteorology/climatology data. Various statistical modeling and analysis procedures, including time series analysis, factor analysis, and regression modeling, were employed. Time series of the constituents were divided into four terms: the long-term mean, the intraannual perturbation, the interannual perturbation, and the synoptic perturbation. PM2.5 at the two sites made up approximately 72% of the total mass for PM10, and the coarse fraction made up the remaining 28%, on average. Thirty-one percent of the PM2.5 at the DC site and 42% at the Shenandoah site was SO4(2-), based on average data for the entire period. At the DC site, the two main contributors to the constituent mass were the long-term mean and the synoptic perturbation terms, and at the Shenandoah site, they were the long-term mean and the intra-annual perturbation terms. This suggested that the constituent mass at the two sites was affected by very different processes. The terms that provided the principal contribution to the constituent mass at the two sites were studied in detail. At the DC site, dew point trends, a climate variable, were the primary driver of the 7-year trends for PM2.5, PM10, the coarse fraction, and total sulfur, and SO2 emission trends were the primary driver of the trends for SO4(2-). SO2 emission trends influenced the trends for PM2.5 and total sulfur, appearing as the second term in the model, but only parameters dealing with climate trends had significant effects on the trends for PM10 and the coarse fraction. At the Shenandoah site, only parameters dealing with climate trends affected long-term particle trends.

Characteristics of Ozone in the Baltimore-Washington Area as Established from One-Hour Average Concentrations.

A 15-year (1981-95) climatology for the diurnal maximum ozone concentration (DMOC) was developed using 1-hr average ozone concentrations in the Baltimore-Washington area, which was made up of four regions: Baltimore, Washington, non-urban Maryland, and non-urban northern Virginia. The DMOC time series for each of these regions were divided into four terms representing different behavioral time scales: the long-term mean; the mean in-tra-annual perturbation; the interannual perturbation; and the synoptic perturbation. The urban regions had smaller values of the long-term mean ozone, but the annual range was larger. The values of the interannual perturbation were largest in the summer, when ozone production is significant, and smallest in the late winter and early spring. The interannual perturbation in the summer in the four regions consistently had positive departures in 1983, 1988, and 1991, and it had negative departures in 1981, 1984, 1985, 1989, 1990, and 1992. Summers with large positive interannual departures experienced a large number of ozone exceedances (i.e., relative to the 1-hr National Ambient Air Quality Standard of 125 parts per billion [ppb]), and summers with large negative departures experienced few or no exceedances. About 50% of the exceedances had concentrations ranging in value from 125-135 ppb, and about 75% had concentrations from 125-145 ppb.