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At least 253 records · Page 14Linked to original sources
USGS2002

Procedures for formation of composite samples from segmented populations

We used a simulation approach to investigate the implication of two methods of forming composite samples to characterize segmented populations. We illustrate the case where the weight of individual segments varies randomly, a situation common with fish samples. Composite samples from segments such as whole fish or muscle tissue should be formed by homogenizing each segment separately and combining equal-sized portions randomly drawn from each homogenate. This approach permits unbiased estimation of the mean concentration per fish. Estimates of mean contaminant concentration varied little with variation in the number of composite samples analyzed or with composite size (number of segments in a composite sample). However, for a fixed number of composite samples, the precision of the variance estimate increases as composite size increased. In addition, for a fixed number of composites, the estimate of the variance stabilized as more segments were included in the composite samples. Estimates of the variance among fish or other population segments can be recovered using appropriate compositing procedures and specially-designed studies.

Environmental Science & Technology↗
USGS2002

Partition of nonpolar organic pollutants from water to soil and sediment organic matters

The partition coefficients (Koc) of carbon tetrachloride and 1,2-dichlorobenzene between normal soil/sediment organic matter and water have been determined for a large set of soils, bed sediments, and suspended solids from the United States and the People's Republic of China. The Koc values for both solutes are quite invariant either for the soils or for the bed sediments; the values on bed sediments are about twice those on soils. The similarity of Koc values between normal soils and between normal bed sediments suggests that natural organic matters in soils (or sediments) of different geographic origins exhibit comparable polarities and possibly comparable compositions. The results also suggest that the process that converts eroded soils into bed sediments brings about a change in the organic matter property. The difference between soil and sediment Koc values provides a basis for identifying the source of suspended solids in river waters. The very high Koc values observed for some special soils and sediments are diagnostic of severe anthropogenic contamination.

Environmental Science & Technology↗
USGS2002

Oxidation of dimethylselenide by δMnO 2 : oxidation product and factors affecting oxidation rate

Volatile dimethylselenide (DMSe) was transformed to a nonvolatile Se compound in a ??-MnO2 suspension. The nonvolatile product was a single compound identified as dimethylselenoxide based on its mass spectra pattern. After 24 h, 100% of the DMSe added to a ??-MnO2 suspension was converted to nonpurgable Se as opposed to 20%, 18%, and 4% conversion for chromate, permanganate, and the filtrate from the suspension, respectively. Manganese was found in solution after reaction. These results imply that the reaction between manganese oxide and DMSe was a heterogeneous redox reaction involving solid phase ??-MnO2 and solution phase DMSe. Oxidation of DMSe to dimethylselenoxide [OSe(CH3)2] by a ??-MnO2 suspension appears to be first order with respect to ??-MnO2, to DMSe, and to hydrogen ion with an overall rate law of d[OSe(CH3)2 ]/dt = 95 M-2 min-1 [MnO2]1[DMSe]1[H+]1 for the MnO2 concentration range of 0.89 ?? 10-3 - 2.46 ?? 10-3 M, the DMSe concentration range of 3.9 ?? 10-7 - 15.5 ?? 10-7 M Se, and a hydrogen ion concentation range of 7.4 ?? 10-6 -9.5 ?? 10-8 M. A general surface site adsorption model is consistent with this rate equation if the uncharged |OMnOH is the surface adsorption site. DMSe acts as a Lewis base, and the manganese oxide surface acts as a Lewis acid. DMSe adsorption to |OMnOH can be viewed as a Lewis acid/ base complex between the largely p orbitals of the DMSe lone pair and the unoccupied eg orbitals on manganese oxide. For such a complex, frontier molecular orbital theory predicts electron transfer to occur via an inner-sphere complex between the DMSe and the manganese oxide. ?? 1995 American Chemical Society.

Environmental Science & Technology↗
USGS2002

Use of the semipermeable membrane device as an in situ sampler of waterborne bioavailable PCDD and PCDF residues at sub-parts-per-quadrillion concentrations

Semipermeable membrane devices (SPMDs) were used to passively sample aqueous polychlorinated dibenzo-p-dioxins (PCDDs) and polychlorinated dibenzofurans (PCDFs) in Bayou Meto, AR. The two sites were upstream and downstream from the confluence with a tributary that delivers PCDDs and PCDFs to the Bayou. Following dialysis, cleanup, and fractionation, four replicate 17-9 SPMD samples from each site were analyzed by GUMS, and four were evaluated by H411E bioassay. Traces of only OCDD and HpCDDs were detected in samples from the upstream site. The four samples from below the tributary contained averages of 1550 ± 80 pg of 2,3,7,8-TCDD, 1640 ± 80 pg of 2,3,7,8-TCDF, and lesser quantities of other congeners. The TCDD equivalents obtained by bioassay of replicate SPMD samples agreed well with results obtained by GC/MS. The quantities of 2,3,7,8- TCDD and 2,3,7,8-TCDF sequestered by SPMDs at the downstream site were used to estimate the aqueous concentrations for both compounds as 2 pg/L.

Environmental Science & Technology↗
USGS2002

Detection of poly(ethylene glycol) residues from nonionic surfactants in surface water by1h and13c nuclear magnetic resonance spectrometry

??? Poly(ethylene glycol) (PEG) residues were detected in organic solute isolates from surface water by 1H nuclear magnetic resonance spectrometry (NMR), 13C NMR spectrometry, and colorimetric assay. PEG residues were separated from natural organic solutes in Clear Creek, CO, by a combination of methylation and chromatographic procedures. The isolated PEG residues, characterized by NMR spectrometry, were found to consist of neutral and acidic residues that also contained poly(propylene glycol) moieties. The 1H NMR and the colorimetric assays for poly(ethylene glycol) residues were done on samples collected in the lower Mississippi River and tributaries between St. Louis, MO, and New Orleans, LA, in July-August and November-December 1987. Aqueous concentrations for poly(ethylene glycol) residues based on colorimetric assay ranged from undetectable to ???28 ??g/L. Concentrations based on 1H NMR spectrometry ranged from undetectable to 145 ??g/L.

Environmental Science & Technology↗
USGS2002

Use of colloid filtration theory in modeling movement of bacteria through a contaminated sandy aquifer

\A filtration model commonly used to describe removal of colloids during packed-bed filtration in water treatment applications was modified for describing downgradient transport of bacteria in sandy, aquifer sediments. The modified model was applied to the results of a small-scale (7 m), natural-gradient tracer test and to observations of an indigenous bacterial population moving downgradient within a plume of organically contaminated groundwater in Cape Cod, MA. The model reasonably accounted for concentration histories of labeled bacteria appearing at samplers downgradient from the injection well in the tracer experiment and for the observed 0.25-μm increase in average cell length for an unlabeled, indigenous bacterial population, 0.6 km downgradient from the source of the plume. Several uncertainties were apparent in applying filtration theory to problems involving transport of bacteria in groundwater. However, adsorption (attachment) appeared to be a major control of the extent of bacterial movement downgradient, which could be described, in part, by filtration theory. Estimates of the collision efficiency factor, which represents the physicochemical factors that determine adsorption of the bacteria onto the grain surfaces, ranged from 5.4 x 10 -3 to 9.7 x 10 -3 .

Environmental Science & Technology↗
USGS2002

Linear solvation energy relationships: "rule of thumb" for estimation of variable values

For the linear solvation energy relationship (LSER), values are listed for each of the variables (V i /100, π*, &beta m , α m ) for fundamental organic structures and functional groups. We give the guidelines to estimate LSER variable values quickly for a vast array of possible organic compounds such as those found in the environment. The difficulty in generating these variables has greatly discouraged the application of this quantitative structure-activity relationship (QSAR) method. This paper present the first compilation of molecular functional group values together with a utilitarian set of the LSER variable estimation rules. The availability of these variable values and rules should facilitate widespread application of LSER for hazard evaluation of environmental contaminants.

Environmental Science & Technology↗
USGS2002

Herbicides in surface waters of the midwestern United States: The effect of spring flush

Approximately three-fourths of all preemergent herbicides used in the United States are applied to row crops over a 12-state area, called the "corn belt" (I). The application of these compounds may cause widespread degradation of water quality (2). Because herbicides are water soluble, there is the potential for leaching into groundwater and surface water (3, 4), as well as aerial transport and Occurrence in precipitation (5). Monitoring studies in the Midwest have shown widespread detection of herbicides in groundwater and in surface water (3,4); however, little is known about the regional impact of herbicide application (6). The objective of our research was to assess the mag. nitude and persistence of herbicide runoff in the spring flush at the regional scale.

Environmental Science & Technology↗