Particulate matter pollution in the coal-producing regions of the Appalachian Mountains: Integrated ground-based measurements and satellite analysis

This study integrates the relationship between measured surface concentrations of particulate matter 10 μm or less in diameter (PM₁₀), satellite-derived aerosol optical depth (AOD), and meteorology in Roda, Virginia, during 2008. A multiple regression model was developed to predict the concentrations of particles 2.5 μm or less in diameter (PM_2.5) at an additional location in the Appalachia region, Bristol, TN. The model was developed by combining AOD retrievals from Moderate Resolution Imaging Spectro-radiometer (MODIS) sensor on board the EOS Terra and Aqua Satellites with the surface meteorological observations. The multiple regression model predicted PM_2.5 (r² = 0.62), and the two-variable (AOD-PM_2.5) model predicted PM_2.5 (r² = 0.4). The developed model was validated using particulate matter recordings and meteorology observations from another location in the Appalachia region, Hazard, Kentucky. The model was extrapolated to the Roda, VA, sampling site to predict PM_2.5 mass concentrations. We used 10 km x 10 km resolution MODIS 550 nm AOD to predict ground level PM_2.5. For the relevant period in 2008, in Roda, VA, the predicted PM_2.5 mass concentration is 9.11 ± 5.16 μg m^-3 (mean ± 1SD).

Implications: This is the first study that couples ground-based Particulate Matter measurements with satellite retrievals to predict surface air pollution at Roda, Virginia. Roda is representative of the Appalachian communities that are commonly located in narrow valleys, or “hollows,” where homes are placed directly along the roads in a region of active mountaintop mining operations. Our study suggests that proximity to heavy coal truck traffic subjects these communities to chronic exposure to coal dust and leads us to conclude that there is an urgent need for new regulations to address the primary sources of this particulate matter.     

Dimer formation during UV photolysis of diclofenac

Dimer formation was observed during ultraviolet (UV) photolysis of the anti-inflammatory drug diclofenac, and confirmed with mass spectrometry, NMR and fluorescence analysis. The dimers were combinations of the two parent molecules or of the parent and the product of photolysis, and had visible color. Radical formation during UV exposure and dissolved oxygen photosensitized reactions played a role in dimer formation. Singlet oxygen formed via photosensitization by photolysis products of diclofenac. It reacted with diclofenac to form an epoxide which is an intermediate in some dimer formation pathways. Quantum yield of photolysis for diclofenac was 0.21 ± 0.02 and 0.19 ± 0.02 for UV irradiation from medium pressure and low pressure mercury vapor lamps, respectively. Band pass filter experiments revealed that the quantum yield is constant at wavelengths >200 nm. The same dimers formed in laboratory grade water when either of the two UV sources was used. Dimers did not form in wastewater effluent matrix, and diclofenac epoxide molecules may have formed bonds with organic matter rather than each other Implications for the importance of dimer formation in NOM are discussed.     

Field Performance of Point Velocity Probes at a Tidally Influenced Site

Conventional methods to estimate groundwater velocity that rely on Darcy's Law and average hydrogeologic parameter values are insensitive to local‐scale heterogeneities and anisotropy that control advective flow velocity and direction. Furthermore, at sites that are tidally influenced or have extraction wells with variable pumping schedules, infrequent water‐level measurements may not adequately characterize the range and significance of transient hydraulic conditions. The point velocity probe (PVP) is a recently developed instrument capable of directly measuring local‐scale groundwater flow velocity and direction. In particular, PVPs may offer distinct advantages for sites with complex groundwater–surface water interactions and/or with spatially and temporally variable groundwater flow conditions. The PVP utilizes a small volume of saline tracer and inexpensive sensors to directly measure groundwater flow direction and velocity in situ at the centimeter‐scale and discrete times. The probes are installed in conventional direct‐push borings, rather than in wells, thus minimizing the changes and biases in the local flow field caused by well installation and construction. Six PVPs were installed at a tidally influenced site in North Carolina to evaluate their implementability, performance, and potential value as a new site characterization tool. For this study, a new PVP prototype was developed using a rapid prototyping machine (i.e., a “three‐dimensional printer'') and included both horizontally and vertically oriented tracer detectors. A site‐specific testing protocol was developed to account for the spatially and temporally variable hydraulic conditions and groundwater salinity. The PVPs were tested multiple times, and the results were compared to the results of several different groundwater flux and velocity estimation tools and methods, including a heat‐pulse flowmeter, passive flux meters, single‐well tracer tests, and high‐resolution hydraulic gradient analysis. Overall, the results confirmed that the PVP concept is valid and demonstrated that reliable estimates of groundwater velocity and direction can be obtained in simple settings. Also, PVPs can be successfully installed by conventional methods at sites where the formation consists primarily of noncohesive soils and the water table is relatively shallow. Although some PVP tests yielded consistent and reliable results, several tests did not. This is likely due to the highly transient flow conditions and limitations associated with the PVP design and testing procedures. PVPs offer particular advantages over, and can effectively complement, other groundwater flow characterization techniques for certain conditions, and objectives may be useful for characterizing complex flow patterns under steady conditions; however, this study suggests that PVPs are best suited for conditions where the flow hydraulics are not highly transient. For sites where the hydraulic conditions are highly transient, the most reliable approach for understanding groundwater flow behavior and groundwater–surface water interactions would generally involve both a high‐resolution hydraulic gradient analysis and another local‐scale method, such as tracer testing. This study also highlighted some aspects of the current PVP design and testing protocol that can be improved upon, including a more robust connection between the PVP and injection line and further assessment of tracer solution density effects on vertical flow. © 2013 Wiley Periodicals, Inc.     

An updated assessment of the acute impacts of ocean carbon sequestration by direct injection

This paper evaluates the expected environmental impact of several promising schemes for ocean carbon sequestration by direct injection of CO₂, and serves as a major update to the assessment by Auerbach et al. (1997) and Caulfield et al. (1997) of water quality impacts and the induced mortality to zooplankton. Three discharge approaches are considered, each designed to maximize dilution over the water column: a point release of negatively buoyant CO₂ hydrate particles from a moving ship; a stationary point release of CO₂ hydrate particles forming a sinking plume; and a long, bottom-mounted diffuser discharging buoyant liquid CO₂ droplets. Two of these scenarios take advantage of the enhanced dilution offered by CO₂ hydrate particles, and are based on recent laboratory and field studies on the formation and behavior of such particles. Overall, results suggest that it is possible with present or near present technology to engineer discharge configurations that achieve sufficient dilution to largely avoid acute impacts. In particular, the moving ship hydrate discharge is identified as the most promising due to its operational flexibility. In addition to lethal effects, sub-lethal and ecosystem effects are discussed qualitatively, though not analyzed quantitatively. Our main conclusion is that ocean carbon sequestration by direct injection should not be dismissed as a climate change mitigation strategy on the basis of environmental impact alone. Rather, it can be considered as a viable option for further study, especially in regions where geologic sequestration proves impractical.     

Optimum swimming pathways of fish spawning migrations in rivers

Fishes that swim upstream in rivers to spawn must navigate complex fluvial velocity fields to arrive at their ultimate locations. One hypothesis with substantial implications is that fish traverse pathways that minimize their energy expenditure during migration. Here we present the methodological and theoretical developments necessary to test this and similar hypotheses. First, a cost function is derived for upstream migration that relates work done by a fish to swimming drag. The energetic cost scales with the cube of a fish's relative velocity integrated along its path. By normalizing to the energy requirements of holding a position in the slowest waters at the path's origin, a cost function is derived that depends only on the physical environment and not on specifics of individual fish. Then, as an example, we demonstrate the analysis of a migration pathway of a telemetrically tracked pallid sturgeon (Scaphirhynchus albus) in the Missouri River (USA). The actual pathway cost is lower than 10(5) random paths through the surveyed reach and is consistent with the optimization hypothesis. The implication--subject to more extensive validation--is that reproductive success in managed rivers could be increased through manipulation of reservoir releases or channel morphology to increase abundance of lower-cost migration pathways.     

Particle laden flows through an inverted chimney with applications to ocean carbon sequestration

Plumes of negatively buoyant hydrate particles, formed by reacting liquid CO₂ with seawater at ocean depths of 1000–1500 m, have been suggested as a way to help sequester CO₂. The vertical flux of CO₂ can be increased by constructing a shroud around the hydrate particle source to shelter the plume from effects of ambient stratification and current. The shroud also serves as an inverted chimney, inducing a down draft that will transport the dissolving particles to a depth of lower ambient disturbance. Laboratory PIV measurements are compared to an analysis of an idealized shroud that is long, frictionless and driven by a single phase source of buoyancy distributed uniformly over the shroud base. Results indicate that induced draft, and hence dilution of dissolved CO₂, increases with plume buoyancy, and shroud length and diameter, but efficiency decreases with increasing ratio of particle slip velocity divided by the characteristic induced draft velocity. While larger particles show reduced plume-like behavior and hence are less efficient in inducing draft, they still generated about half of the theoretically predicted flow.     

A low-maintenance,primary cell culture model for the assessment of carbon nanotube toxicity

Carbon nanotubes (CNTs) have gained substantial interest as a material for biomedical devices with reliable properties suitable for electrically conducting biomedical devices. While CNTs combine ideal properties for a number of tissue-interfacing applications, their biocompatibility and safety have been the source of considerable conjecture. This study outlines a method for evaluating biocompatibility, using a low-cost, short-term assessment model of CNT with primary cells, which are more representative of an in vivo situation than cell lines. It was demonstrated that carboxylate-modified, multi-walled CNTs exhibit cytotoxic behavior in as little as 6 hr of exposure to primary fibroblasts. The resultant cell death was concentration dependent, demonstrating the efficacy of acute assessment of cytocompatibility. Although cell viability remained relatively high (being above 85% for all CNT concentrations up to 500 μg/ml), these results reflect similar relationships found for longer term exposures. This method has reliable potential for high-throughput assessment and quality control of CNTs in biomedical applications using a primary cell model.     

Integrated approach to PCE‐impacted site characterization,site management,and enhanced bioremediation

Tetrachloroethene (PCE)‐ and trichloroethene (TCE)‐impacted sites pose significant challenges even when site characterization activities indicate that biodegradation has occurred naturally. Although site‐specific, regulatory, and economic factors play roles in the remedy‐selection process, the application of molecular biological tools to the bioremediation field has streamlined the assessment of remedial alternatives and allowed for detailed evaluation of the chosen remedial technology. The case study described here was performed at a PCE‐impacted site at which reductive dechlorination of PCE and TCE had led to accumulation of cis‐dichlorethene (cis‐DCE) with concentrations ranging from approximately 10 to 100 mg/L. Bio‐Trap® samplers and quantitative polymerase chain reaction (qPCR) enumeration of Dehalococcoides spp. were used to evaluate three remedial options: monitored natural attenuation, biostimulation with HRC®, and biostimulation with HRC‐S®. Dehalococcoides populations in HRC‐S‐amended Bio‐Traps deployed in impacted wells were on the order of 10³ to 10⁴ cells/bead but were below detection limits in most unamended and HRC‐amended Bio‐Traps. Thus the in situ Bio‐Trap study identified biostimulation with HRC‐S as the recommended approach, which was further evaluated with a pilot study. After the pilot HRC‐S injection, Dehalococcoides populations increased to 10⁶ to 10⁷ cells/bead, and concentrations of cis‐DCE and vinyl chloride decreased with concurrent ethene production. Based on these results, a full‐scale HRC‐S injection was designed and implemented at the site. As with the pilot study, full‐scale HRC‐S injection promoted growth of Dehalococcoides spp. and stimulated reductive dechlorination of the daughter products cis‐DCE and vinyl chloride. © 2008 Wiley Periodicals, Inc.     

Geographic distribution of selected elements in the livers of polar bears from Greenland, Canada and the United States

To assess geographic distributions of elements in the Arctic we compared essential and non-essential elements in the livers of polar bears (Ursus maritimus) collected from five regions within Canada in 2002, in Alaska between 1994 and 1999 and from the northwest and east coasts of Greenland between 1988 and 2000. As, Hg, Pb and Se varied with age, and Co and Zn with gender, which limited spatial comparisons across all populations to Cd, which was highest in Greenland bears. Collectively, geographic relationships appeared similar to past studies with little change in concentration over time in Canada and Greenland for most elements; Hg and Se were higher in some Canadian populations in 2002 as compared to 1982 and 1984. Concentrations of most elements in the polar bears did not exceed toxicity thresholds, although Cd and Hg exceeded levels correlated with the formation of hepatic lesions in laboratory animals.