Mapping Odor Sources from Complaint Statistics I: Identifying the Major Source

Odor is acknowledged as a major community air pollution nuisance, but the problems of analysis, particularly in Identifying the origin of odor, are also well recognised. One approach to the problem has been the development of computational schemes which use wind directions at the times of odor observations to locate the likely source of odor. An earlier technique, PONG, has now been superseded by a more sophisticated version, PONG2, which incorporates Gaussian plume modeling techniques. This paper describes the operation of PONG2 in the odor source mapping mode and provides an analysis of the Insensitivity of the technique to errors in input. Then, using specific Australian examples of community odor nuisance emanating from a large sewage treatment complex near Melbourne, and an irrigated golf course within metropolitan Darwin, the paper outlines the utility of PONG2 in resolving problem odor sources at a range of scales and levels of complexity.     

Degradation of octylphenol and nonylphenol by ozone - part I: direct reaction

This aqueous reaction between ozone and two alkylphenols (APs), namely octylphenol (OP) and nonylphenol (NP), has been investigated. Both compounds are important endocrine disrupting chemicals, which arise from the biodegradation of alkylphenol ethoxylates and are often found at relatively high concentrations in wastewater effluents. In this paper the results of an experimental study are presented which provide values for the reaction rate constants between molecular ozone and undissociated OP and NP, and overall reaction rate constants for the degradation of the two APs at pH values in the range of 7-9. The kinetic rate constants for OP and NP degradation by molecular ozone were 4.33(+/-0.18) x 10(4) and 3.90(+/-0.10) x 10(4) M(-1) s(-1), and the reaction stoichiometry was similar in both cases and equal to approximately 1.3:1 ([O3]:[AP]). The overall second order reaction rate constants for the two APs increased significantly with increasing pH, which is believed to be mainly due to the increasing influence of indirect radical reaction with increasing pH; this aspect is considered in more detail in a companion paper. A preliminary investigation of the reaction mechanism suggests that an initial product of ozonation is hydroxyl-alkyl phenol.     

Electrolytic debromination of PBDEs in DE-83 technical decabromodiphenyl ether

Electrochemical debromination of the commercial decabromodiphenyl ether flame retardant DE-83 in partly aqueous tetrahydrofuran (THF) solution gave lower brominated congeners by sequential loss of bromine atoms. Hydrodebromination was most facile for the most heavily brominated congeners. It involves initial electron transfer and proton transfer from water, rather than hydrogen atom abstraction from THF, as shown by experiments with deuterated water. The product distribution from electrolysis involves preferential loss of bromine meta- and para- to the ether linkage, comparable with the products of metabolism of BDE-209 in various organisms. Significantly, the environmentally relevant congeners BDE-47, BDE-99, and BDE-154 were not major products of debromination of BDE-209 by the electron transfer mechanism.     

Convergent and Contingent Community Responses to Grass Source and Dominance During Prairie Restoration Across a Longitudinal Gradient

Restoring prairie on formerly cultivated land begins by selecting propagule seed sources and the diversity of species to reintroduce. This study examined the effects of dominant grass propagule source (cultivar vs. non-cultivar) and sown propagule diversity (grass:forb sowing ratio) on plant community structure. Two field experiments were established in Kansas and Illinois consisting of identical split plot designs. Dominant grass source was assigned as the whole-plot factor, and sown dominance of grasses (five levels of seeded grass dominance) as the subplot factor. Species density, cover, and diversity were quantified for 5 years. The effect of dominant grass source on the cover of focal grasses, sown species, and volunteer species was contingent upon location, with variation between dominant grass sources observed exclusively in Kansas. Species density and diversity showed regionally convergent patterns in response to dominant grass source. Contrary to our hypotheses, total species density and diversity were not lower in the presence of grass cultivars, the grass source we had predicted would be more competitive. Sown grass dominance effects on the cover of the focal grass species were contingent upon location resulting from establishment corresponding better to the assigned treatments in Illinois. All other cover groups showed regionally convergent patterns, with lower cover of volunteers and higher cover of sown forbs, diversity, and species density in the lowest sown grass dominance treatment in both sites. Thus, decisions regarding the diversity of propagules to reintroduce had more consequence for plant community structure than cultivar or non-cultivar source of dominant grasses.     

Cultivating hybrid collectives: research methods for enacting community food economies in Australia and the Philippines

Across the globe, groups are experimenting with initiatives to create alternatives to the dominant food system. What role might research play in helping to strengthen and multiply these initiatives? In this paper we discuss two research projects in Australia and the Philippines in which we have cultivated hybrid collectives of academic researchers, lay researchers and various non-human others with the intention of enacting community food economies. We feature three critical interactions in the “hybrid collective research method”: gathering, which brings together those who share concerns about community food economies; reassembling, in which material gathered is deliberatively rebundled to amplify particular insights; and translating, by which reassembled ideas are taken up by other collectives so they may continue to “do work”. We argue that in a climate-changing world, the hybrid collective research method fosters opportunities for a range of human and non-human participants to act in concert to build community food economies.     

Balancing environmental and industry sustainability: A case study of the US gold mining industry

Mandatory insurance requirements and/or mitigation fees (royalties) for mining companies may help reduce environmental risk exposure for the federal government. Mining is examined since the Environmental Protection Agency (EPA) Toxic Release Inventory reveals that this sector produces more hazardous waste than any other industrial sector. Although uncommon, environmental expense can exceed hundreds of millions of dollars per development. Of particular concern is the potential for mines to become unfunded Superfund sites. Monte Carlo simulation of risk exposure is used to establish a plausible range of unfunded federal liabilities associated with cyanide-leach gold mining. A model is developed to assess these costs and their impact on both the federal budget and corporate profitability (i.e., industry sustainability), particularly if such costs are borne by offending firms.     

Evaluating LNAPL contamination using GPR signal attenuation analysis and dielectric property measurements: practical implications for hydrological studies

Groundwater and sub-surface contamination by Light Non-Aqueous Phase Liquids (LNAPLs) is one of the industrial world's most pressing environmental issues and a thorough understanding of the hydrological, physical and bio-chemical properties of the sub-surface is key to determining the spatial and temporal development of any particular contamination event. Non-invasive geophysical techniques (such as electrical resistivity, electromagnetic conductivity, Ground-Penetrating Radar, etc.) have proved to be successful sub-surface investigation and characterisation tools with Ground-Penetrating Radar (GPR) being particularly popular. Recent studies have shown that the spatial/temporal variation in GPR signal attenuation can provide important information on the electrical properties of the sub-surface materials that, in turn, can be used to assess the physical and hydrological nature of the pore fluids and associated contaminants. Unfortunately, a high percentage of current LNAPL-related GPR studies focus on contaminant mapping only, with little emphasis being placed on characterising the hydrological properties (e.g., determining contaminant saturation index, etc.). By comparing laboratory-based, dielectric measurements of LNAPL contaminated materials with the GPR signal attenuation observed in both contaminated and 'clean' areas of an LNAPL contaminated site, new insights have been gained into the nature of contaminant distribution/saturation and the likely signal attenuation mechanisms. The results show that, despite some practical limitations of the analysis technique, meaningful hydrological interpretations can be obtained on the contaminant properties, saturation index and bio-degradation processes. A generalised attenuation/saturation model has been developed that describes the physical and attenuation enhancement characteristics of the contaminated areas and reveals that the most significant attenuation is related to smeared zone surrounding the seasonally changing water table interface. It is envisaged that the model will provide a basis for the interpretation of GPR data from analogous LNAPL contaminated sites and provide investigators with an appreciation of the merits and limitations of GPR-based, attenuation analysis techniques for hydrological applications.     

Reaction pathways of dimethyl phthalate degradation in TiO2-UV-O2 and TiO2-UV-Fe(VI) systems

The photocatalytic degradation of dimethyl phthalate (DMP) in aqueous TiO₂ suspension under UV illumination has been investigated using oxygen (O₂) and ferrate (Fe(VI)) as electron acceptors. The experiments demonstrated that Fe(VI) was a more effective electron acceptor than O₂ for scavenging the conduction band electrons from the surface of the catalyst. Some major intermediate products from DMP degradation were identified by HPLC and GC/MS analyses. The analytical results identified dimethyl 3-hydroxyphthalate and dimethyl 2-hydroxyphthalate as the two main intermediate products from the DMP degradation in the TiO₂–UV–O₂ system, while in contrast phthalic acid was found to be the main intermediate product in the TiO₂–UV–Fe(VI) system. These findings indicate that DMP degradation in the TiO₂–UV–O₂ and TiO₂–UV–Fe(VI) systems followed different reaction pathways. An electron spin resonance analysis confirmed that hydroxyl radicals existed in the TiO₂–UV–O₂ reaction system and an unknown radical species (most likely an iron–oxo species) is suspected to exist in the TiO₂–UV–Fe(VI) reaction system. Two pathway schemes of DMP degradation in the TiO₂–UV–O₂ and TiO₂–UV–Fe(VI) reaction systems are proposed. It is believed that the radicals formed in the TiO₂–UV–O₂ reaction system preferably attack the aromatic ring of the DMP, while in contrast the radicals formed in the TiO₂–UV–Fe(VI) reaction systems attack the alkyl chain of DMP.