Relationship between the ATP content of subsurface material and the rate of biodegradation of alkylbenzenes and chlorobenzene

The rate of biotransformation of toluene in unconsolidated subsurface material from sites at Lula, Oklahoma, and Conroe, Texas, was compared to the ATP (adenosine triphosphate) content of these materials. The rate of toluene degradation decreased with decreasing ATP content. When ATP contents were at or less than 0.05 ng g⁻¹, biotransformation of toluene could not be detected (less than 1% of the initial concentration was degraded per week). At intermediate concentrations of ATP, 0.37 and 0.16 ngvg⁻¹, the rates of toluene degradation were 18 ± 4.5% and 25 ± 10% of the initial concentration per week. At ATP concentrations above 1 ng g⁻¹, the rates of toluene degradation exceeded 90% of the initial concentration per week. There was no simple relationship between ATP content and chlorobenzene degradation. Subsurface material that had been exposed to creosote wastes, and which degraded toluene rapidly, also degraded benzene, o-xylene, and m-xylene.     

Prediction of PCB content in sportfish using semipermeable membrane devices (SPMDs)

Triolein-filled semipermeable membrane devices (SPMDs) were immersed at three locations along the St. Joseph River in northern Indiana for 30 days to see if the PCB content of fish from the same location could be predicted with this model device. Triolein from the SPMD's was analyzed for PCB using enzyme-linked immunosorbent assay (ELISA) and compared to residues detected in fish collected from the same locations. There was a significant difference (p < 0.05) in total PCB concentrations between SPMD samples. However, due to variability in PCB residues between species and low PCB residues in SPMDs, a direct correlation between PCBs in sportfish and SPMDs could not be determined.     

Effects of rooting medium and fertilizer rate on response of white clover to tropospheric ozone

Two white clover (Trifolium repens L.) clones with varying sensitivity to O(3) are being developed as a system to indicate effects of ambient concentrations of tropospheric O(3) on plants. One clone (NC-S) is highly sensitive to O(3) and the other (NC-R) is highly resistant. The system relies on periodic measurement of foliar injury, foliar chlorophyll, and forage production of NC-S and NC-R grown in 15-liter pots throughout a summer season. Relative amounts of foliar injury and ratios (NC-S/NC-R) for chlorophyll and forage weight can be used to estimate biologically effective ambient O(3) concentrations. The effect of variation in rooting media formulation and fertilizer rate on response of NC-S and NC-R to ambient O(3) was determined in the present study. In the rooting medium experiment, clover was grown in three mixtures of sandy loam topsoil:course washed sand:Metro Mix 220 (ratios (by volume) of 2:1:1, 2:1:5, and 6:1:1). In the fertilizer experiment, clover was grown in the 2:1:1 medium at four fertilizer rates (soluble 5-11-26 (N-P-K) at 0.0, 0.5, 1.0, or 2.0 g per pot). Ozone caused more foliar injury, more chlorosis, and a greater decrease in forage production of NC-S than of NC-R in all studies. Rooting media treatments affected both clones similarly and occasional clone x media interactions were judged to be random. Forage production by NC-S, relative to that of NC-R, was generally greater in the 0.0 fertilizer treatment, but the forage ratios were similar at all other fertilizer treatments. The relative response of NC-S and NC-R to O(3) is fairly stable under cultural conditions that support normal plant growth.     

Sorption of hydrophobic organic pollutants in saturated soil systems

Sorption equilibria and rates were characterized for a matrix of four aquifer sands and two slightly to moderately hydrophobic organic solutes (nitrobenzene and lindane), and the effects of sorption on the behavior of these solutes in saturated systems of the soils were determined. Experimental data were used to test and evaluate a variety of mathematical models for predicting contaminant fate and transport in groundwater systems.Observed equilibrium relationships between soil and solution phase solute concentrations were found to be described best by the nonlinear Freundlich isotherm model. It was further determined that the sorption process in the systems tested is rate controlled, requiring several days to approach equilibrium in completely mixed batch reactors. Subsequent modeling of solute transport in continuous flow soil column reactors was found to be most successful when rate-controlled models were used, the best results were obtained with a dual-resistance model incorporating the coupled mass transport steps of boundary-layer and intraparticle diffusion.     

Accumulation of potentially toxic elements in plants and their transfer to human food chain.

Contaminated soils can be a source for crop plants of such elements like As, Cd, Cr, Cu, Ni, Pb, and Zn. The excessive transfer of As, Cu, Ni, and Zn to the food chain is controlled by a "soil-plant barrier"; however, for some elements, including Cd, the soil-plant barrier fails. The level of Cd ingested by average person in USA is about 12 micrograms/day, which is relatively low comparing to Risk Reference Dose (70 micrograms Cd/day) established by USEPA. Food of plant origin is a main source of Cd intake by modern society. Fish and shellfish may be a dominant dietary sources of Hg for some human populations. About half of human Pb intake is through food, of which more than half originates from plants. Dietary intake of Cd and Pb may be increased by application of sludges on cropland with already high levels of these metals. Soils amended with sludges in the USA will be permitted (by USEPA-503 regulations) to accumulate Cr, Cd, Cu, Pb, Hg, Ni, and Se, and Zn to levels from 10 to 100 times the present baseline concentrations. These levels are very permissive by international standards. Because of the limited supply of toxicity data obtained from metals applied in sewage sludge, predictions as to the new regulations will protect crop plants from metal toxicities, and food chain from contamination, are difficult to make.     

Butyltins in estuarine sediments two years after tributyltin use was restricted

The highly toxic compound tributyltin (TBT) is the active agent in many effective antifouling paints. In 1988 the U.S. regulated its use in such paints. Sediments taken from four sites in Boston Harbor, MA., USA in the summer of 1990 were assayed for organotins. There was significantly less TBT at all sites in 1990 than there was in 1988. Dibutyltin (DBT) and monobutyltin (MBT), were also detected, confirming that TBT degradation occurs in the estuary. It is suggested that the decreases are due to biological and/or chemical mechanisms rather than to photochemical reactions or transport away from the sites on resuspended particulate matter.     

Determination of PCDDs and PCDFs in PCB oil from a hazardous waste site

This paper describes the analysis of hazardous waste oil samples with procedures that were developed primarily to clean up and analyze biological samples. Details of the cleanup procedure and the results from the analysis of several waste PCB oil samples are presented.     

Impact of engine lubricant properties on regulated gaseous emissions of 2000-2001 model-year gasoline vehicles

The impact of the sulfur (S) content in lubricating oil was evaluated for four ultra-low-emission vehicles and two super-ultra-low-emission vehicles, all with low mileage. The S content in the lube oils ranged from 0.01 to 0.76%, while the S content of the gasoline was fixed at 0.2 ppmw. Vehicles were configured with aged catalysts and tested over the Federal Test Procedure, at idle and at 50-mph cruise conditions. In all testing modes, variations in the S level of the lubricant did not significantly affect the regulated gas-phase tailpipe emissions. In addition to the regulated gas-phase emissions, a key element of the research was measuring the engine-out sulfur dioxide (SO2) in near-real-time. This research used a new methodology based on a differential optical absorption spectrometer (DOAS) to measure SO2 from the lubricants used in this study. With the DOAS, the contribution of SO2 emissions for the highest-S lubricant was found to range from less than 1 to 6 ppm on a gasoline S equivalent basis over the range of vehicles and test cycles used. The development and operation of the DOAS is discussed in this paper.     

Computation of the interfacial area for two-fluid porous medium systems

We develop a method to compute interfacial areas from three-dimensional digital representations of multiphase systems. We approximate the interfaces with the isosurface generated by the standard marching-cube algorithm from the discrete phase distribution. We apply this approach to two-fluid pore-scale simulations by (1) simulating a random packing of spheres that obeys the grain-size distribution and porosity of an experimental porous medium system, and (2) using a previously developed pore-morphology-based model in order to predict the phase distribution for a water-wet porous medium that undergoes primary drainage. The predicted primary drainage curve and interfacial areas are in good agreement with the experimental values reported in the literature, where interfacial areas were measured using interfacial tracers. The energy dissipation during Haines jumps is significant: thus, the mechanical work done on the system is not completely converted into surface energy, and interfacial areas may not be deduced from the primary drainage curve.