An approach for determining bioassessment performance and comparability

Many organizations in the USA collect aquatic bioassessment data using different sampling and analysis methods, most of which have unknown performance in terms of data quality produced. Thus, the comparability of bioassessments produced by different organizations is often unknown, ultimately affecting our ability to make comprehensive assessments on large spatial scales. We evaluated a pilot approach for determining bioassessment performance using macroinvertebrate data obtained from several states in the Southeastern USA. Performance measures evaluated included precision, sensitivity, and responsiveness to a human disturbance gradient, defined in terms of a land disturbance index value for each site, combined with a value for specific conductance, and instream habitat quality. A key finding of this study is the need to harmonize ecoregional reference conditions among states so as to yield more comparable and consistent bioassessment results. Our approach was also capable of identifying potential areas for refinement such as reevaluation of less precise, sensitive, or responsive metrics that may result in suboptimal index performance. Higher performing bioassessments can yield information beyond “impaired” versus “unimpaired” condition. Acknowledging the limitations of this pilot study, we would recommend that performance evaluations use at least 50 sites, 10 of which are ecoregional reference sites. Efforts should be made to obtain data from the entire human disturbance gradient in an ecoregion to improve statistical confidence in performance measures. Having too few sites will result in an under-representation of certain parts of the disturbance gradient (e.g., too few poor quality sites), which may bias sensitivity and responsiveness estimates.     

An Investigation of Idle Emissions Inspection and Maintenance at Altitude

Idle emissions inspection and maintenance was evaluated using a sample of 300 privately owned 1964 through 1973 model-year vehicles operating in the Denver metropolitan area. Ten privately owned stations, licensed by the State of Colorado to perform vehicle safety inspections, were utilized to conduct idle emissions inspection and subsequent maintenance of failed vehicles. Exhaust hydrocarbon (HC) and carbon monoxide (CO) reduction as measured by the 1975 Environmental Protection Agency (EPA) mass emission testing procedures was indicated to be 13% and 8% respectively at a 50 % rejection rate. The average maintenance cost to achieve the reduction was $11.32 per failed vehicle.

The adjustment and repair procedures provided to participating garages were sufficient to achieve significant emissions reduction and training provided to garage personnel was adequate. However, several problems were experienced with station personnel relative to data transmittal and inspection pass/fail limits. Problems were also experienced with respect to correlations between laboratory and garage-type analytical instrumentation.     

Public Reaction to SIP Revisions for Ozone Reduction

ABSTRACT

This study utilized a biotrickling filter with blast-furnace slag packings (sizes = 20-40 mm; specific surface area = 120 m²/m³) to treat toluene in an air stream. Also studied were the effects of volumetric loading (L), nutrient addition, and superficial gas velocity (U_g) or gas retention time on toluene elimination capacity. Experimental results indicate that, for a test period of 121 days, with no excess biomass removal, toluene removal efficiencies of over 90% were obtained with U_g < 80 m/hr and L < 30 g/m³.hr. For a test period of 49 days, with U_g < 80 m/hr and L increased from 1.2 to 81 g/m³.hr, the absence of nutrient supplementation did not limit the toluene elimination capacity. Nutrients stored in the biofilm could adequately support the microbial activity for the toluene elimination. According to data regression, a simplified mass-transfer model is proposed, which correlates the contaminant concentration with the packing height or gas empty bed retention time. As verified, the model proposed herein can be applied to cases involving low influent contaminant concentrations or loadings to the extent that none or only a trace amount of the contaminant can be found in the recirculation liquid. Although small media with larger specific surface areas can achieve a better mass transfer, the problems of frequent backwashing and relatively greater gas resistance in using this type of media probably outweigh the advantages, particularly for full-scale systems that would not be watched as closely as laboratory test systems.     

Validation of Mobile Source Emission Estimates Using Mass Balance Techniques

Air quality models must consider error in the emissions estimates as well as in the model itself. Currently, the accepted method for determining emission factors for mobile sources is through the use of the EPA model MOBILE₃. In this paper, emission factor calculations from a technique based on the conservation of mass are presented from experimental data. These emission factors are then compared to MOBILE₃ simulations using the experimental conditions and two different methods of obtaining the vehicle scenario. In both cases, the mass balance gave emission factors that were from 1.5 to 2.2 times those predicted by MOBILE₃. Next, mass balance and MOBILE₃ emission factors were used in the dispersion models CALINE3 and TXLINE in an effort to predict the observed CO concentrations. In both models, enhanced performance was observed when mass balance data were implemented.     

Quantification and characterization of vehicle-based polycyclic aromatic hydrocarbons (PAHs) in street dust from the Tamale metropolis,Ghana

Objective

Concentrations of polycyclic aromatic hydrocarbons (PAHs) in street dust in the Tamale metropolis, Ghana, have been measured in this study.

Results

The concentrations of the various types of PAHs identified in street dust samples from high vehicular traffic density in the metropolis are as follows: naphthalene, 10,000 μg/kg; acenaphthylene, 13,000 μg/kg; acenaphthene, 76,000 μg/kg; fluorene, 18,900 μg/kg; phenanthrene, 40,000 μg/kg; anthracene, 21,000 μg/kg; fluoranthene, 35,200 μg/kg; pyrene, 119,000 μg/kg; benzo[a]anthracene, 17,700 μg/kg; chrysene, 10,600 μg/kg; benzo[k]fluoranthene, 18,700 μg/kg; benzo[a]pyrene, 10,900 μg/kg and benzo[g, h, i]perylene, 21,000 μg/kg. Calculation of the phenanthrene/anthracene ratio indicated that the PAHs identified in this study were from vehicular fallout as the ratio was less than 10.

Conclusion

It is clear from the results of the study that road users in the Tamale metropolis, especially hawkers, are exposed to the harmful effects of PAHs, and this suggests the need for the establishment of mitigation measures by the regulatory agencies.

     

Comparison of DAYCENT-simulated and measured nitrous oxide emissions from a corn field

Accurate assessment of N(2)O emission from soil requires continuous year-round and spatially extensive monitoring or the use of simulation that accurately and precisely predict N(2)O fluxes based on climatic, soil, and agricultural system input data. DAYCENT is an ecosystem model that simulates, among other processes, N(2)O emissions from soils. The purpose of the study was to compare N(2)O fluxes predicted by the DAYCENT model to measured N(2)O fluxes from an experimental corn field in central Iowa. Soil water content temperature and inorganic N, simulated by DAYCENT were compared to measured values of these variables. Field N(2)O emissions were measured using four replicated automated chambers at 6-h intervals, from day of year (DOY) 42 through DOY 254 of 2006. We observed that DAYCENT generally accurately predicted soil temperature, with the exception of winter when predicted temperatures tended to be lower than measured values. Volumetric water contents predicted by DAYCENT were generally lower than measured values during most of the experimental period. Daily N(2)O emissions simulated by DAYCENT were significantly correlated to field measured fluxes; however, time series analyses indicate that the simulated fluxes were out of phase with the measured fluxes. Cumulative N(2)O emission calculated from the simulations (3.29 kg N(2)O-N ha(-1)) was in range of the measured cumulative N(2)O emission (4.26 +/- 1.09 kg N(2)O-N ha(-1)).     

Mercury in Tree Swallow Food, Eggs, Bodies, and Feathers at Acadia National Park, Maine, and an EPA Superfund Site, Ayer, Massachusetts

We monitored nest boxes during 1997–1999 at Acadia National Park, Mt. Desert Island, ME and at an old-field site in Orono, ME to determine mercury (Hg) uptake in tree swallow (Tachycineta bicolor) eggs, tissues, and food boluses. Also, in 1998–1999 we monitored nest boxes at Grove Pond and Plow Shop Pond at a U.S. Environmental Protection Agency Superfund site in Ayer, MA. We recorded breeding success at all locations. On average among locations, total mercury (THg) biomagnified 2 to 4-fold from food to eggs and 9 to 18-fold from food to feathers. These are minimum values because the proportion of transferable methyl mercury (MeHg) of the THg in insects varies (i.e., 35%–95% of THg) in food boluses. THg was highest in food boluses at Aunt Betty Pond at Acadia, whereas THg in eggs was highest at the Superfund site. A few eggs from nests at each of these locations exceeded the threshold (i.e., 800–1,000 ng/g, wet wt.) of embryotoxicity established for Hg. Hatching success was 88.9% to 100% among locations, but five eggs failed to hatch from 4 of the 11 clutches in which an egg exceeded this threshold. MeHg in feathers was highest in tree swallows at Aunt Betty Pond and the concentration of THg in bodies was related to the concentration in feathers. Transfer of an average of 80%–92% of the Hg in bodies to feathers may have enhanced nestling survival. Residues of Hg in tissues of tree swallows in the Northeast seem higher than those of the Midwest.     

Disruption of the global nitrogen cycle: A grand challenge for the twenty-first century: This article belongs to Ambio’s 50th Anniversary Collection. Theme: Eutrophication

Disruption of the global nitrogen cycle by humans results primarily from activities associated with food and energy production. Since the middle of the twentieth century, human activities have more than doubled inputs of nitrogen to the Earth’s ecosystems. This new nitrogen is in chemically and biologically active forms (reactive N) and moves through the environment causing an array of health and environmental problems. Research published in Ambio for the past three decades has been documenting this major global-scale problem and has catalyzed the formation of a science-led initiative, the International Nitrogen Initiative (INI), which has informed policies to manage the global nitrogen cycle. Currently, gaps and opportunities in nitrogen pollution policies still exist and require new interdisciplinary science to help to place the nitrogen management challenge in the context of the other environmental grand challenges of our time including climate change and biodiversity loss because their solutions will be interconnected.     

Dynamism of household carbon emissions (HCEs) from rural and urban regions of northern and southern China

China contributes 23 % of global carbon emissions, of which 26 % originate from the household sector. Due to vast variations in both climatic conditions and the affordability and accessibility of fuels, household carbon emissions (HCEs) differ significantly across China. This study compares HCEs (per person) from urban and rural regions in northern China with their counterparts in southern China. Annual macroeconomic data for the study period 2005 to 2012 were obtained from Chinese government sources, whereas the direct HCEs for different types of fossil fuels were obtained using the IPCC reference approach, and indirect HCEs were calculated by input-output analysis. Results suggest that HCEs from urban areas are higher than those from rural areas. Regardless of the regions, there is a similarity in per person HCEs in urban areas, but the rural areas of northern China had significantly higher HCEs than those from southern China. The reasons for the similarity between urban areas and differences between rural areas and the percentage share of direct and indirect HCEs from different sources are discussed. Similarly, the reasons and solutions to why decarbonising policies are working in urban areas but not in rural areas are discussed.

     

Ambient air concentrations of polychlorinated dibenzo-p-dioxins and dibenzofurans in Ohio: Sources and health risk assessment

PCDD and PCDF were measured in air samples collected in Ohio in 1987. No 2,3,7,8-TCDD was detected in any of the samples with a detection limits of less than 240 fg/m³. Using a chemical mass balance model applied to PCDD/PCDF congener group profiles, major potential sources of these compounds to the atmosphere in Ohio were determined to be municipal solid waste combustion, and sewage sludge combustion. Cancer risk calculations for inhalation of PCDD/PCDF in ambient air in Ohio are approximately 10–6. Given the current knowledge of the health effects of exposure to PCDD/PCDF in air, there is no appreciable risk to public health for the levels of these compounds found in ambient air in Ohio.