RIVER-QUALITY ASSESSMENTS1

ABSTRACT: In 1972, the U.S. Geological Survey began a pilot program of river-quality assessments. The objectives of the program are (1) to define the character, interrelationships, and apparent causes of existing river-quality problems, and (2) to devise and demonstrate the analytical approaches and the tools and methodologies needed for developing water-quality information that will provide a sound technical basis for planners and managers to use in assessing river-quality problems and evaluating management alternatives. The most noteworthy finding of a pilot assessment of the Willamette River basin, Oregon, was that across-the-board advanced waste treatment was not the answer to the problem of meeting stringent water-quality standards established for the river. The assessment also found that existing water-quality data generally are inadequate for defining the critical cause-effect relationships that control river-quality problems and that intensive, synoptic surveys keyed to local problems and conditions would be required in most river basins to develop an adequate information base for managing important river-quality problems. The study illustrated that rigid nationwide standards and regulations are likely to result in unneeded expenditures in some river basins and in undesirable quality in others.     

Combined thermal and zero‐valent iron In Situ soil mixing remediation technology

Thermal remediation of contaminated soils and groundwater by injection of hot air and steam using large‐diameter auger in situ soil mixing effectively remediates volatile and semivolatile organic compounds. This technology removes large amounts of contamination during the early treatment stages, but extended treatment times are needed to achieve high removal percentages. Combining thermal treatment with another technology that can be injected and mixed into the soil, and that continues to operate after removal of the drilling equipment, improves removal efficiency, and reduces cost. Using field‐determined pseudo first‐order removal rates, the cost of the combined remediation of chlorinated volatile organic compounds (CVOCs) by thermal treatment followed by reductive dechlorination by iron powder has been estimated as 57 percent of the cost of thermal treatment alone. This analysis was applied to a case‐study remediation of 48,455 cubic yards, which confirmed the cost estimate of the combined approach and showed over 99.8 percent removal of trichloroethene and other chlorinated VOCs. © 2010 Wiley Periodicals, Inc.     

Emissions of volatile fatty acids from feed at dairy facilities

Recent studies suggest that dairy operations may be a major source of non-methane volatile organic compounds in dairy-intensive regions such as Central California, with short chain carboxylic acids (volatile fatty acids or VFAs) as the major components. Emissions of four VFAs (acetic acid, propanoic acid, butanoic acid and hexanoic acid) were measured from two feed sources (silage and total mixed rations (TMR)) at six Central California Dairies over a fifteen-month period. Measurements were made using a combination of flux chambers, solid phase micro-extraction fibers coupled to gas chromatography mass spectrometry (SPME/GC–MS) and infra-red photoaccoustic detection (IR-PAD for acetic acid only). The relationship between acetic acid emissions, source surface temperature and four sample composition factors (acetic acid content, ammonia-nitrogen content, water content and pH) was also investigated. As observed previously, acetic acid dominates the VFA emissions. Fluxes measured by IR-PAD were systematically lower than SPME/GC–MS measurements by a factor of two. High signals in field blanks prevented emissions from animal waste sources (flush lane, bedding, open lot) from being quantified. Acetic acid emissions from feed sources are positively correlated with surface temperature and acetic acid content. The measurements were used to derive a relationship between surface temperature, acetic acid content and the acetic acid flux. The equation derived from SPME/GC–MS measurements predicts estimated annual average acetic acid emissions of (0.7 + 1/?0.4) g m^?2 h^?1 from silage and (0.2 + 0.3/?0.1) g m^?2 h^?1 from TMR using annually averaged acetic acid content and meteorological data. However, during the summer months, fluxes may be several times higher than these values.     

Spatial and temporal variability of outdoor coarse particulate matter mass concentrations measured with a new coarse particle sampler during the Detroit Exposure and Aerosol Research Study

The Detroit Exposure and Aerosol Research Study (DEARS) provided data to compare outdoor residential coarse particulate matter (PM_10–2.5) concentrations in six different areas of Detroit with data from a central monitoring site. Daily and seasonal influences on the spatial distribution of PM_10–2.5 during Summer 2006 and Winter 2007 were investigated using data collected with the newly developed coarse particle exposure monitor (CPEM). These data allowed the representativeness of the community monitoring site to be assessed for the greater Detroit metro area. Multiple CPEMs collocated with a dichotomous sampler determined the precision and accuracy of the CPEM PM_10–2.5 and PM_2.5 data.CPEM PM_2.5 concentrations agreed well with the dichotomous sampler data. The slope was 0.97 and the R² was 0.91. CPEM concentrations had an average 23% negative bias and R² of 0.81. The directional nature of the CPEM sampling efficiency due to bluff body effects probably caused the negative CPEM concentration bias.PM_10–2.5 was observed to vary spatially and temporally across Detroit, reflecting the seasonal impact of local sources. Summer PM_10–2.5 was 5 μg m^?3 higher in the two industrial areas near downtown than the average concentrations in other areas of Detroit. An area impacted by vehicular traffic had concentrations 8 μg m^?3 higher than the average concentrations in other parts of Detroit in the winter due to the suspected suspension of road salt. PM_10–2.5 Pearson Correlation Coefficients between monitoring locations varied from 0.03 to 0.76. All summer PM_10–2.5 correlations were greater than 0.28 and statistically significant (p-value < 0.05). Winter PM_10–2.5 correlations greater than 0.33 were statistically significant (p-value < 0.05). The PM_10–2.5 correlations found to be insignificant were associated with the area impacted by mobile sources during the winter. The suspected suspension of road salt from the Southfield Freeway, combined with a very stable atmosphere, caused concentrations to be greater in this area compared to other areas of Detroit. These findings indicated that PM_10–2.5, although correlated in some instances, varies sufficiently across a complex urban airshed that that a central monitoring site may not adequately represent the population's exposure to PM_10–2.5.     

Ambient Air Quality at the Site of a Former Manufactured Gas Plant

Prior to the 1950's, manufactured gas was commerciallyproduced from the pyrolysis of coal, coke, and oil atfacilities that are termed manufactured gas plants (MGPs). The constituents of residual coal tar present on many MGPsites are an environmental health concern because of theirtoxicity and the possibility for their off-site migration viawater and air. Atmospheric concentrations of five volatileorganic compounds (VOCs, e.g., benzene), sixteen polycyclicaromatic hydrocarbons (PAHs, e.g., naphthalene), and particulate matter less than 10 microns in aerodynamicdiameter (PM₁₀) were measured at the site of a former MGP. Air samples were obtained before, during, and after excavationof subterranean coal tar at the site. The results of thisinvestigation indicate that subterranean coal tar was not aprimary source of VOCs and PAHs in the local atmosphere beforeor after remediation of the site. However, excavation,treatment, blending, and transfer of the coal tar duringremediation generated concentrations of selected aromatic andsemi-volatile organic compounds that were substantiallygreater than typical ambient levels. In addition, these datasuggest that blending and mixing of coal tars could lead toexceedance of the U.S. National Ambient Air Quality Standardfor PM₁₀, although additional research is required to fullyevaluate this possibility. Nuisance odors associated with thesite remediation were likely the result of naphthalene andpossibly isomers of xylene. Air pollutant concentrationsmeasured adjacent to the excavation area and at the siteperimeter during remediation activities were less than therelevant occupational and environmental exposure limits.     

A new synthesis of tetrachlorofluorodibenzo‐p‐dioxin

Abstract

The 1,2,3,4‐tetrachloro‐7‐fluorodibenzo‐p‐dioxin has been synthesized via condensation of 4‐fluorocatechol and pentachloronitrobenzene. This compound could be used as an internal standard for the analysis of 2,3,7,8‐tetrachlorodibenzo‐p‐dioxin by Chromatographic methods.     

Hydrologic Modeling Uncertainty Resulting From Land Cover Misclassification1

Abstract: A stochastic, spatially explicit method for assessing the impact of land cover classification error on distributed hydrologic modeling is presented. One‐hundred land cover realizations were created by systematically altering the North American Landscape Characterization land cover data according to the dataset’s misclassification matrix. The matrix indicates the probability of errors of omission in land cover classes and is used to assess the uncertainty in hydrologic runoff simulation resulting from parameter estimation based on land cover. These land cover realizations were used in the GIS‐based Automated Geospatial Watershed Assessment tool in conjunction with topography and soils data to generate input to the physically‐based Kinematic Runoff and Erosion model. Uncertainties in modeled runoff volumes resulting from these land cover realizations were evaluated in the Upper San Pedro River basin for 40 watersheds ranging in size from 10 to 100 km² under two rainfall events of differing magnitudes and intensities. Simulation results show that model sensitivity to classification error varies directly with respect to watershed scale, inversely to rainfall magnitude and are mitigated or magnified by landscape variability depending on landscape composition.