Loading estimates of lead, copper, cadmium, and zinc in urban runoff from specific sources

Urban stormwater runoff is being recognized as a substantial source of pollutants to receiving waters. A number of investigators have found significant levels of metals in runoff from urban areas, especially in highway runoff. As an initiatory study, this work estimates lead, copper, cadmium, and zinc loadings from various sources in a developed area utilizing information available in the literature, in conjunction with controlled experimental and sampling investigations. Specific sources examined include building siding and roofs; automobile brakes, tires, and oil leakage; and wet and dry atmospheric deposition. Important sources identified are building siding for all four metals, vehicle brake emissions for copper and tire wear for zinc. Atmospheric deposition is an important source for cadmium, copper, and lead. Loadings and source distributions depend on building and automobile density assumptions and the type of materials present in the area examined. Identified important sources are targeted for future comprehensive mechanistic studies. Improved information on the metal release and distributions from the specific sources, along with detailed characterization of watershed areas will allow refinements in the predictions.     

Distribution and bioaccumulation of selenium in aquatic microcosms

Closed-system microcosms were used to study factors affecting the fate of selenium (Se) in aquatic systems. Distribution and bioaccumulation of Se varied among sediment types and Se species. A mixture of dissolved (75)Se species (selenate, selenite and selenomethionine) was sorbed more rapidly to fine-textured, highly organic pond sediments than to sandy riverine sediments. Sulfate did not affect the distribution and bioaccumulation of (75)Se over the range 80-180 mg SO(4) liter(-1). When each Se species was labeled separately, selenomethionine was lost from the water column more rapidly than selenate or selenite. Selenium lost from the water column accumulated primarily in sediments, but volatilization was also an important pathway for loss of Se added as selenomethionine. Loss rates of dissolved Se residues were more rapid than rates reported from mesocosm and field studies, suggesting that sediment: water interactions are more important in microcosms than in larger test systems. Daphnids accumulated highest concentrations of Se, followed by periphyton and macrophytes. Selenium added as selenomethionine was bioaccumulated preferentially compared to that added as selenite or selenate. Organoselenium compounds such as selenomethione may thus contribute disproportionately to Se bioaccumulation and toxicity in aquatic organisms.     

Characterization and pyrolysis of Chlorella vulgaris and Arthrospira platensis: potential of bio-oil and chemical production by Py-GC/MS analysis

Environmental Science and Pollution Research - Biofuels have been seen as potential sources to meet future energy demand as a renewable and sustainable energy source. Despite the fact that the...     

Negative ion chemical ionization mass spectrometry - a useful technique for the selective detection of polar substituted polycyclic aromatic hydrocarbons with mutagenic properties

Earlier studies have shown that many compounds with toxic properties are able to form stable negative ions. The negative ion mass spectrometric response of polar substances found in indoor air extracts from aluminium smelters was determined and compared with available mutagenicity data. The results indicate that the relationship mentioned above also is valid for polar compounds.     

Effects of selected pesticides on Rhizobiummeliloti, and on seed germination and Verticillium wilt pathogens of alfalfa

Studies on the effects of 21 fungicides and five pyrethroid insecticides on growth of $\text{Rhizobium}$$\text{meliloti}$, emergence and survival of alfalfa seed and the efficacy of the chemicals in control of Verticillium wilt pathogens were conducted.     

Simulation of organic liquid flow in porous media using estimated and measured transport properties

Many numerical models which describe the movement of a separate organic liquid phase in the subsurface require information about the relationships between capillary pressure and saturation, and between relative permeability and saturation. An evaluation of the information available for these relationships suggests that substantial discrepancies may be introduced into simulations if estimated, rather than measured, data are employed. The purpose of this study was to quantify these deviations. Two-phase displacement simulations were performed in one and two dimensions for several organic liquid-water systems. Both constant-head and constant-flux boundary conditions were employed at a variety of flow rates and time scales, using both measurements and estimates of capillary pressure and relative permeability for a sandy aquifer material. The results demonstrate that the use of estimated transport relationships produces significantly different predictions of organic liquid migration. The magnitude of the deviations between predictions may be as high as 25% or more after relatively short displacement periods, depending on the boundary conditions of the simulated scenario, as well as on the physical characteristics of the two-phase system. For the systems examined, most of the deviations resulted from the estimates for relative permeability to the organic liquid. Thus, improved methods for the estimation of the relative permeability to the organic liquid are needed to reduce the uncertainty in displacement simulations.     

Lung-deposited dose of particulate matter from residential exposure to smoke from wood burning

Environmental Science and Pollution Research - Residential settings are of utmost importance for human exposure, as it is where people spend most of their time. Residential wood combustion is a...