Natural attenuation of chlorinated solvents at Area 6, Dover Air Force Base: characterization of microbial community structure

A polyphasic approach based on cultivation and direct recovery of 16S rRNA gene sequences was utilized for microbial characterization of an aquifer contaminated with chlorinated ethenes. This work was conducted in order to support the evaluation of natural attenuation of chlorinated ethenes in groundwater at Area 6 at Dover Air Force Base (Dover, DE). Results from these studies demonstrated the aquifer contained relatively low biomass (e.g. direct microscopic counts of < 10(7) bacteria/g of sediment) comprised of a physiologically diverse group of microorganisms including iron reducers, acetogens, sulfate reducers, denitrifiers, aerobic and anaerobic heterotrophs. Laboratory microcosms prepared with authentic sediment and groundwater provided direct microbiological evidence that the mineralization of vinyl chloride and cis-dichloroethene as well as each step in the complete reductive dechlorination of tetracloroethene to ethene can occur in the Area 6 aquifer. Enrichment cultures capable of the oxidative degradation of cis-1,2-dichloroethene (cis-DCE) and vinyl chloride (VC) were obtained from groundwater across the aquifer demonstrating the possible importance of direct, non-cometabolic oxidation of cis-DCE and VC in natural attenuation. Culture-independent analyses based upon recovery of 16S rRNA gene sequences revealed the presence of anaerobic organisms distributed primarily between two major bacterial divisions: the delta subdivision of the Proteobacteria and low-G + C gram positive. Recovery of sequences affiliated with phylogenetic groups containing known anaerobic-halorespiring organisms such as Desulfitobacterium, Dehalobacter, and certain groups of iron reducers provided qualitative support for a role of reductive dechlorination processes in the aquifer. This molecular data is suggestive of a functional linkage between the microbiology of the site and the apparent natural attenuation process. The presence and distribution of microorganisms were found to be consistent with a microbially driven attenuation of chlorinated ethenes within the aquifer and in accord with a conceptual model of aquifer geochemistry which suggest that both reductive and oxidative mechanisms are involved in heterogeneous, spatially distributed processes across the aquifer.     

Muskox status,recent variation,and uncertain future

Ambio - Muskoxen (Ovibos moschatus) are an integral component of Arctic biodiversity. Given low genetic diversity, their ability to respond to future and rapid Arctic change is unknown, although...     

Biodegradability and toxicity assessment of trans-chlordane photochemical treatment

The removal of trans-chlordane (C(10)H(6)Cl(8)) from aqueous solutions was studied using UV, UV/H(2)O(2), UV/H(2)O(2)/Fe(2+), UV/TiO(2), or UV/TiO(2)/H(2)O(2) treatment using either UV/Vis blue lamps or UVC lamps (254 nm). H(2)O(2), FeSO(4) and TiO(2) were added at 1700, 456, and 2500 mgL(-1), respectively. trans-Chlordane was not significantly removed in non-irradiated controls and in samples irradiated with UV/Vis. It was also not removed in the absence of surfactant Triton X-114 added at 250 mgL(-1). In the presence of the surfactant, trans-chlordane concentration was reduced by 95-100% after 48 h of UVC and UVC/H(2)O(2) treatments and 70-80% after UVC/H(2)O(2)/Fe(2+), UVC/TiO(2) and UVC/H(2)O(2)/TiO(2) treatments. Based on these results, UVC, UVC/H(2)O(2) and UVC/TiO(2) treatments were further investigated. UVC treatment supported the highest pollutant removal (100% in 48 h), dechlorination efficiency (81% in 48 h), and detoxification to Lepidium sativum seed germination and activated sludge respiration although irradiated samples remained toxic to Chlorella vulgaris. Biodegradation of the UVC irradiated samples removed the source of algae toxicity but this could not be clearly attributed to the removal of trans-chlordane photoproducts because the surfactant interfered with the chemical and biological assays. Evidence was found that trans-chlordane was photodegraded through photolysis causing its successive dechlorination. trans-Chlordane removal was well described by a first order kinetic model at a rate of 0.21±0.01h(-1) at the 95% confidence interval.     

Predicting Ringelmann Number and Optical Characteristics of Plumes

Methods have been developed for calculating the Ringelmann number, opacity, and other optical characteristics of stack plumes from information on particulate properties, concentrations, and system geometry. Such calculations can be used in selecting clean-up equipment to improve stack appearance required to meet Ringelmann number and opacity pollution regulations. Methods were developed for white plumes caused by water drops or crystalline material and for black plumes containing carbon emissions. The Mie theory of light scattering was utilized to calculate plume optical properties which were related to Ringelmann number through psycophysically significant correlations. A computer program was written to perform the Mie theory and related calculations. Graphical methods were developed for plumes with log-probability size distributions composed of water drops, dusts with refractive index of 1.50 or carbon type emissions of refractive index 1.59-0.66i. Agreement of Ringelmann numbers predicted by these techniques and those observed for large stacks is excellent.     

Influence of regional development policies and clean technology adoption on future air pollution exposure

Future air pollution emissions in the year 2030 were estimated for the San Joaquin Valley (SJV) in central California using a combined system of land use, mobile, off-road, stationary, area, and biogenic emissions models. Four scenarios were developed that use different assumptions about the density of development and level of investment in transportation infrastructure to accommodate the expected doubling of the SJV population in the next 20 years. Scenario 1 reflects current land-use patterns and infrastructure while scenario 2 encouraged compact urban footprints including redevelopment of existing urban centers and investments in transit. Scenario 3 allowed sprawling development in the SJV with reduced population density in existing urban centers and construction of all planned freeways. Scenario 4 followed currently adopted land use and transportation plans for the SJV. The air quality resulting from these urban development scenarios was evaluated using meteorology from a winter stagnation event that occurred on December 15th, 2000 to January 7th 2001. Predicted base-case PM2.5 mass concentrations within the region exceeded 35 μg m^?3 over the 22-day episode. Compact growth reduced the PM2.5 concentrations by ～1 μg m^?3 relative to the base-case over most of the SJV with the exception of increases (～1 μg m^?3) in urban centers driven by increased concentrations of elemental carbon (EC) and organic carbon (OC). Low-density development increased the PM2.5 concentrations by 1–4 μg m^?3 over most of the region, with decreases (0.5–2 μg m^?3) around urban areas. Population-weighted average PM2.5 concentrations were very similar for all development scenarios ranging between 16 and 17.4 μg m^?3. Exposure to primary PM components such as EC and OC increased 10–15% for high density development scenarios and decreased by 11–19% for low-density scenarios. Patterns for secondary PM components such as nitrate and ammonium ion were almost exactly reversed, with a 10% increase under low-density development and a 5% decrease under high density development. The increased human exposure to primary pollutants such as EC and OC could be predicted using a simplified analysis of population-weighted primary emissions. Regional planning agencies should develop thresholds of population-weighted primary emissions exposure to guide the development of growth plans. This metric will allow them to actively reduce the potential negative impacts of compact growth while preserving the benefits.     

Predicting black smoke levels from deposit gauge and SO2 data to estimate long-term exposure in the United Kingdom, 1956–1961

BackgroundIn the UK air quality has been monitored systematically since 1914, providing valuable data for studies of the long-term trends in air pollution and potentially for studies of health effects of air pollutants. There are, however, challenges in interpreting these data due to changes over time in the number and location of monitored sites, and in monitoring techniques. Particulate matter was measured as deposited matter (DM) using deposit gauge monitors until the 1950s when black smoke (BS) filters were introduced. Estimating long-term exposure to particulates using data from both deposit gauge and BS monitors requires an understanding of the relationships between DM, SO₂ and BS.AimsTo explore whether DM and/or SO₂, along with seasonal and location specific variables can be used to predict BS levels.MethodsAir quality data were abstracted from hard copies of the monthly Atmospheric Pollution Bulletins for the period April 1956–March 1961 for any sites with co-located DM, SO₂ and BS data for three or more consecutive years. The relationships between DM, SO₂, and BS were assessed using mixed models.ResultsThere were 34 eligible sites giving 1521 triplets of data. There was a consistent correlation between SO₂ and BS at all sites, but the association between DM and BS was less clear and varied by location. Mixed modelling allowing for repeat measurements at each site revealed that SO₂, year, rainfall and season of measurement explained 72% of the variability in BS levels.ConclusionsSO₂ can be used as a surrogate measure for BS in all monitoring locations. This surrogate can be improved upon by consideration of site specific characteristics, seasonal effects, rainfall and year of measurement. These findings will help in estimating historic, long-term exposure to particulates where BS or other measures are not available.     

Melamine-based organoclay to sequester atrazine

Sequestration of aqueous atrazine by organoclays prepared from the surfactant 6-piperazin-1-yl-N,N'-bis-(1,1,3,3-tetramethyl-butyl)-(1,3,5)triazine-2,4-diamine and Gonzales bentonite was assessed using 14C-labeled atrazine. Organoclays with varying ratios of surfactant to clay were evaluated with respect to their ability to sequester atrazine from an aqueous solution. Organoclays containing 100-200 g kg-1 surfactant on a total weight basis provided the most efficient adsorption of atrazine, with apparent KOC values exceeding 5000 l kg-1 at these loading fractions. Less than 12% of sequestered atrazine was released during four sequential day long washings, supporting our expectation that the majority of the reaction of atrazine with the surfactant lead to irreversible chemical bond formation through nucleophilic aromatic substitution.