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G.D. Foster

Publications and source records attributed to G.D. Foster.

5 recordsLinked to original sources

Use of field-applied quality control samples to monitor performance of a Goulden large-sample extractor/GC-MS method for pesticides in water

Since 1985, the Goulden large-sample extractor (GLSE) has been used to isolate a broad array of trace-organic contaminants from large volumes of water. In this study, field-applied quality control measures, including matrix and surrogate spikes and blanks, were used to monitor method performance from GLSE extraction through GC-MS analysis. The method was applied to the determination of multiple classes of pesticides isolated from 4- to 112-L filtered surface-water samples. Average recoveries of six surrogate compounds ranged from 84 ?? 18% for [2H10]diazinon to 15 ?? 13% for 4,4'-[2H8]DDT, the low recoveries for which were largely a result of unmonitored breakdown of this surrogate by the GC injection system. Field-matrix-spike samples were prepared by fortifying 10-L, 35-L, and 110-L filtered surface-water samples with 68 pesticides to amended concentrations of 11- to 50-ng/L each. Recoveries ranged from not detected to greater than 100%. Variability in pesticide recoveries from triplicate 10-L water samples collected at one site averaged 5.7% relative standard deviation and did not exceed 19%.Since 1985, the Goulden large-sample extractor (GLSE) has been used to isolate a broad array of trace-organic contaminants from large volumes of water. In this study, field-applied quality control measures, including matrix and surrogate spikes and blanks, were used to monitor method performance from GLSE extraction through GC-MS analysis. The method was applied to the determination of multiple classes of pesticides isolated from 4- to 112-L filtered surface-water samples. Average recoveries of six surrogate compounds ranged from 84 ?? 18% for [2H10]diazinon to 15 ?? 13% for 4,4???-[2H8]DDT, the low recoveries for which were largely a result of unmonitored breakdown of this surrogate by the GC injection system. Field-matrix-spike samples were prepared by fortifying 10-L, 35-L, and 110-L filtered surface-water samples with 68 pesticides to amended concentrations of 11- to 50-ng/L each. Recoveries ranged from not detected to greater than 100%. Variability in pesticide recoveries from triplicate 10-L water samples collected at one site averaged 5.7% relative standard deviation and did not exceed 19%.

International Journal of Environmental Analytical

Baseflow and stormflow metal fluxes from two small agricultural catchments in the Coastal Plain of the Chesapeake Bay Basin, United States

Annual yields (fluxes per unit area) of Al, Mn, Fe, Ni, Cd, Pb, Zn, Cu, Cr, Co, As and Se were estimated for two small non-tidal stream catchments on the Eastern Shore of the Chesapeake Bay, United States - a poorly drained dissected-upland watershed in the Nanticoke River Basin, and a well-drained feeder tributary in the lower reaches of the Chester River Basin. Both watersheds are dominated by agriculture. A hydrograph-separation technique was used to determine the baseflow and stormflow components of metal yields, thus providing important insights into the effects of hydrology and climate on the transport of metals. Concentrations of suspended-sediment were used as a less-costly proxy of metal concentrations which are generally associated with particles. Results were compared to other studies in Chesapeake Bay and to general trends in metal concentrations across the United States. The study documented a larger than background yield of Zn and Co from the upper Nanticoke River Basin and possibly enriched concentrations of As, Cd and Se from both the upper Nanticoke River and the Chesterville Branch (a tributary of the lower Chester River). The annual yield of total Zn from the Nanticoke River Basin in 1998 was 18,000 g/km2/a, and was two to three times higher than yields reported from comparable river basins in the region. Concentrations of Cd also were high in both basins when compared to crustal concentrations and to other national data, but were within reasonable agreement with other Chesapeake Bay studies. Thus, Cd may be enriched locally either in natural materials or from agriculture.

Applied Geochemistry

Pesticides, polycyclic aromatic hydrocarbons, and polychlorinated biphenyls in transport in two Atlantic coastal plain tributaries and loadings to Chesapeake Bay

Concentrations of current-use pesticides, polycyclic aromatic hydrocarbons (PAHs), polychlorinated biphenyls (PCBs), and organochlorine (OC) insecticides were determined above the reach of tide in the Chesterville Branch and Nanticoke River on the eastern shore of Chesapeake Bay during base-flow and storm-flow hydrologic regimes to evaluate mass transport to Chesapeake Bay. The two rivers monitored showed relatively high concentrations of atrazine, simazine, alachlor, and metolachlor in comparison to previously investigated western shore tributaries, and reflected the predominant agricultural land use in the eastern shore watersheds. The four current use pesticides showed the greatest seasonal contribution to annual loadings to tidal waters of Chesapeake Bay from the two rivers, and the relative order of annual loadings for the other contaminant classes was PAHs > PCBs > OC insecticides. Annual loadings normalized to the landscape areas of selected Chesapeake Bay watersheds showed correlations to identifiable source areas, with the highest pesticide yields (g/km2/yr) occurring in eastern shore agricultural landscapes, and the highest PAH yields derived from urban regions.

Journal of Environmental Science and Health - Part

Performance of the goulden large-sample extractor in multiclass pesticide isolation and preconcentration from stream water

The reliability of the Goulden large-sample extractor in preconcentrating pesticides from water was evaluated from the recoveries of 35 pesticides amended to filtered stream waters. Recoveries greater than 90% were observed for many of the pesticides in each major chemical class, but recoveries for some of the individual pesticides varied in seemingly unpredictable ways. Corrections cannot yet be factored into liquid-liquid extraction theory to account for matrix effects, which were apparent between the two stream waters tested. The Goulden large-sample extractor appears to be well suited for rapid chemical screening applications, with quantitative analysis requiring special quality control considerations. ?? 1991 American Chemical Society.

Journal of Agricultural and Food Chemistry

Seasonal concentrations of organic contaminants at the fall line of the Susquehanna River basin and estimated fluxes to northern Chesapeake Bay, USA

Riverine fluxes of several pesticides and other organic contaminants from above the fall line of the Susquehanna River basin to northern Chesapeake Bay, USA, were quantified in 1994. Base flow and storm flow samples collected at the fall line of the river from February to December 1994 were analyzed for both dissolved and particulate phase contaminants. Measured concentrations of the organonitrogen and organophosphorus pesticides varied mainly in response to the timing of their application to agricultural fields. Conversely, the concentrations of the more particle-sorptive contaminants such as polychlorinated biphenyls (PCBs), organochlorine (OC) insecticides, and polycyclic aromatic hydrocarbons (PAHs) were more directly correlated with river flow throughout the year. Annual fluxes were almost entirely in the dissolved phase for the organonitrogen and organophosphorus pesticides, distributed between the dissolved and particulate phases for the PCBs and OC insecticides, and primarily in the particulate phase for the PAHs.

Maryland, New Jersey, New York, Pennsylvania, Virg