Measurement of Photochemical Air Pollution with a Sensitive Monitoring Plant

With newly developed monitoring techniques, investigators used the sensitive tobacco variety, Bel-W3, as a monitor for photochemical air pollution at different locations within 75 miles of Cincinnati, Ohio. Observations during the summers of 1966 through 1968 revealed almost daily injury to monitoring plants, fairly uniform total seasonal injury at all locations, and a marked variation in both oxidant and injury from one season to another within the city. The relationship between oxidant level and injury was not found to be consistent.     

Coastal construction trends in response to coastal erosion: an opportunity for adaptation

In Florida, more than half of the state’s sandy beach coastlines are designated as critical erosion areas by the Florida Department of Environmental Protection (FDEP 2008). At the same time, the economic contribution of coastal construction is being confounded by the fiscal peril facing Florida (Bird in Ann Geomorph 57:1–9, 1985, Pew Center on the States 2009, U.S BEA 2009). It is therefore an opportune time for an evaluation of coastal erosion policy response which specifically addresses coastal construction. Furthermore in Florida, an increasing coastal population requiring the provision of structural development necessitates an improved understanding of how legislative intent which avoids the cumulative impacts of development is translated through quantified policy response. This study characterizes how coastal development trends in Florida have responded to critical erosion designation. Using spatial and temporal analysis of coastal construction permitting data from 1987 to 2007, three coastal counties in northwest Florida were selected for this study. This selection was based on proximity to the designated ecologically sensitive Apalachicola National Estuarine Research Reserve (ANERR). This study has indicated that clusters of development have not been reduced or redirected by critical erosion designation in certain areas of the study counties. Therefore this study has implications for the regulatory framework governing coastal development permitting in Florida, which is of timely relevance for sea-level rise adaptation.     

Large emissions of sesquiterpenes and methyl chavicol quantified from branch enclosure measurements

Multiple field studies have suggested chemistry within a forest canopy is poorly understood due to inadequate detection and quantification of reactive biogenic emissions, such as terpenes. To measure emission rates of terpenes at Blodgett Forest, a coniferous forest in the Sierra Nevada mountains of California, we placed enclosures over branches of the dominant species at the site – Ponderosa pine, manzanita, and ceanothus – in the summer of 2005. Zero air, with ambient CO₂ concentrations, flowed through the chamber system and volatile organic compound (VOC) emission measurements were made by proton transfer reaction mass spectrometry (PTR-MS), solid phase microextraction (SPME) on fibers followed by direct injection into a gas chromatograph with an ion trap mass spectrometer (GC-ITMS), and by in situ GC with a flame ionization detector (GC-FID). We show that previously undetected sesquiterpenes and methyl chavicol significantly contribute to the total reactive biogenic emission profile from this field site.     

The impact of wood stove technology upgrades on indoor residential air quality

Fine particulate matter (PM_2.5) air pollution has been linked to adverse health impacts, and combustion sources including residential wood-burning may play an important role in some regions. Recent evidence suggests that indoor air quality may improve in homes where older, non-certified wood stoves are exchanged for lower emissions EPA-certified alternatives. As part of a wood stove exchange program in northern British Columbia, Canada, we sampled outdoor and indoor air at 15 homes during 6-day sampling sessions both before and after non-certified wood stoves were exchanged. During each sampling session two consecutive 3-day PM_2.5 samples were collected onto Teflon filters, which were weighed and analyzed for the wood smoke tracer levoglucosan. Residential PM_2.5 infiltration efficiencies (F_inf) were estimated from continuous light scattering measurements made with nephelometers, and estimates of F_inf were used to calculate the outdoor- and indoor-generated contributions to indoor air. There was not a consistent relationship between stove technology and outdoor or indoor concentrations of PM_2.5 or levoglucosan. Mean F_inf estimates were low and similar during pre- and post-exchange periods (0.32 ± 0.17 and 0.33 ± 0.17, respectively). Indoor sources contributed the majority (～65%) of the indoor PM_2.5 concentrations, independent of stove technology, although low indoor-outdoor levoglucosan ratios (median ≤ 0.19) and low indoor PM_2.5-levoglucosan correlations (r ≤ 0.19) suggested that wood smoke was not a major indoor PM_2.5 source in most of these homes. In summary, despite the potential for extensive wood stove exchange programs to reduce outdoor PM_2.5 concentrations in wood smoke-impacted communities, we did not find a consistent relationship between stove technology upgrades and indoor air quality improvements in homes where stoves were exchanged.     

Colombia's discharge fee program: Incentives for polluters or regulators?

Colombia's discharge fee system for water effluents is often held up as a model of a well-functioning, economic incentive pollution control program in a developing country. Yet few objective evaluations of the program have appeared. Based on a variety of primary and secondary data, this paper finds that in its first 5 years, the program was beset by a number of serious problems including limited implementation in many regions, widespread noncompliance by municipal sewerage authorities, and a confused relationship between discharge fees and emissions standards. Nevertheless, in some watersheds, pollution loads dropped significantly after the program was introduced. While proponents claim the incentives that discharge fees created for polluters to cut emissions in a cost-effective manner were responsible, this paper argues that the incentives they created for regulatory authorities to improve permitting, monitoring, and enforcement were at least as important.     

Occurrence of arsenic and phosphorus in ditch flow from litter-amended soils and barn areas

Little is known about the fate of arsenic (As) in land-applied litter from chickens that have been fed roxarsone, an organic feed additive containing As. This study seeks to elucidate the transfer of As in runoff from ditch-drained soils of the poultry-producing region of the Delmarva Peninsula by tracking As and phosphorus (P) export from seven drainage ditches over two water-years (1 July 2005 to 30 June 2007). Annual losses of As from ditches ranged from 0.004 to 0.071 kg ha(-1) while P losses ranged from 0.33 to 18.56 kg ha(-1), with the largest loads associated with a litter storage shed that served as a point source. Event-based As and P losses in ditch flow fluctuated by a factor of 162 and 1882, respectively. The two elements were correlated in flow from the ditch draining a litter storage shed (r = 0.99), and in sediment extracts in soils near the litter shed (r = 0.73), pointing to similar behavior under point source conditions. Indeed, As and P exhibited similar behavior within storms for all ditches, characterized by relatively high initial concentrations subject to rapid concentration declines before peak flow, consistent with dilution of a finite source. However, As and P concentrations varied significantly between ditches and showed considerable temporal variability within ditches, with no clear seasonal trends or associations with current management strategies. The results suggest that similar management strategies might be effective for As and P point sources, but that field management practices geared toward controlling nonpoint source P losses may not readily transfer to the control of As losses.     

Application of OMI observations to a space-based indicator of NOx and VOC controls on surface ozone formation

We investigated variations in the relative sensitivity of surface ozone formation in summer to precursor species concentrations of volatile organic compounds (VOCs) and nitrogen oxides (NO_x) as inferred from the ratio of the tropospheric columns of formaldehyde to nitrogen dioxide (the “Ratio”) from the Aura Ozone Monitoring Instrument (OMI). Our modeling study suggests that ozone formation decreases with reductions in VOCs at Ratios <1 and NO_x at Ratios >2; both NO_x and VOC reductions may decrease ozone formation for Ratios between 1 and 2. Using this criteria, the OMI data indicate that ozone formation became: 1. more sensitive to NO_x over most of the United States from 2005 to 2007 because of the substantial decrease in NO_x emissions, primarily from stationary sources, and the concomitant decrease in the tropospheric column of NO₂, and 2. more sensitive to NO_x with increasing temperature, in part because emissions of highly reactive, biogenic isoprene increase with temperature, thus increasing the total VOC reactivity. In cities with relatively low isoprene emissions (e.g., Chicago), the data clearly indicate that ozone formation became more sensitive to NO_x from 2005 to 2007. In cities with relatively high isoprene emissions (e.g., Atlanta), we found that the increase in the Ratio due to decreasing NO_x emissions was not obvious as this signal was convolved with variations in the Ratio associated with the temperature dependence of isoprene emissions and, consequently, the formaldehyde concentration.     

Updating the conceptual model for fine particle mass emissions from combustion systems

Atmospheric transformations determine the contribution of emissions from combustion systems to fine particulate matter (PM) mass. For example, combustion systems emit vapors that condense onto existing particles or form new particles as the emissions are cooled and diluted. Upon entering the atmosphere, emissions are exposed to atmospheric oxidants and sunlight, which causes them to evolve chemically and physically, generating secondary PM. This review discusses these transformations, focusing on organic PM. Organic PM emissions are semi-volatile at atmospheric conditions and thus their partitioning varies continuously with changing temperature and concentration. Because organics contribute a large portion of the PM mass emitted by most combustion sources, these emissions cannot be represented using a traditional, static emission factor. Instead, knowledge of the volatility distribution of emissions is required to explicitly account for changes in gas-particle partitioning. This requires updating how PM emissions from combustion systems are measured and simulated from combustion systems. Secondary PM production often greatly exceeds the direct or primary PM emissions; therefore, secondary PM must be included in any assessment of the contribution of combustion systems to ambient PM concentrations. Low-volatility organic vapors emitted by combustion systems appear to be very important secondary PM precursors that are poorly accounted for in inventories and models. The review concludes by discussing the implications that the dynamic nature of these PM emissions have on source testing for emission inventory development and regulatory purposes. This discussion highlights important linkages between primary and secondary PM, which could lead to simplified certification test procedures while capturing the emission components that contribute most to atmospheric PM mass.