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Publications

Dive into our publications and explore the science from the Environmental Health Program (Toxic Substances Hydrology and Contaminant Biology).

Filter Total Items: 3787

Hydrogeologic and water-quality data used to evaluate the effects of focused recharge on ground-water quality near Princeton, Minnesota, 1991-95

This study was part of the Management Systems Evaluation Area (MSEA) Program, a multi-scale, inter-agency initiative to evaluate the effects of agricultural systems on water quality in the midwest corn belt. The research was part of the U.S. Geological Survey Toxics Substances Hydrology Program. The research area was located in the Anoka Sand Plain about 5 kilometers southwest of Princeton, Minnes
Authors
G. N. Delin, M.K. Landon, K.J. Nelson, R. B. Wanty, R. W. Healy, H.W. Olson, J.K. Böhlke, B. R. Schroyer, P. D. Capel

Identification of ionic chloroacetanilide-herbicide metabolites in surface water and groundwater by HPLC/MS using negative ion spray

Solid-phase extraction (SPE) was combined with high-performance liquid chromatography/high-flow pneumatically assisted electrospray mass spectrometry (HPLC/ESP/MS) for the trace analysis of oxanilic and sulfonic acids of acetochlor, alachlor, and metolachlor. The isolation procedure separated the chloroacetanilide metabolites from the parent herbicides during the elution from C18 cartridges using
Authors
Imma Ferrer, E.M. Thurman, Damià Barceló

Source characterization of disinfection byproduct precursors in two Arkansas water-supply reservoirs

No abstract available.
Authors
Michael L. Pomes, W. R. Green, E.M. Thurman, W. H. Orem, H.T. Lerch

Nuclear magnetic resonance identification of new sulfonic acid metabolites of chloroacetanilide herbicides

The detection of the sulfonic acid metabolites of the chloroacetanilide herbicides acetochlor, alachlor, butachlor, propachlor, and, more recently, metolachlor in surface and ground water suggests that a common mechanism for dechlorination exists via the glutathione conjugation pathway. The identification of these herbicides and their metabolites is important due to growing public awareness and co
Authors
M.D. Morton, F.H. Walters, D.S. Aga, E.M. Thurman, C.K. Larive

Herbicides and their metabolites in rainfall: Origin, transport, and deposition patterns across the midwestern and northeastern United States, 1990-1991

Herbicides were detected in rainfall throughout the midwestern and northeastern United States during late spring and summer of 1990 and 1991. Herbicide concentrations exhibited distinct geographic and seasonal patterns. The highest concentrations occurred in midwestern cornbelt states following herbicide application to cropland. Volume-weighted concentrations of 0.2−0.4 μg/L for atrazine and alach
Authors
D. A. Goolsby, E.M. Thurman, M.L. Pomes, M. T. Meyer, W.A. Battaglin

Terbuthylazine and deethylterbuthylazine in rain and surface water: Determination by enzyme immunoassay and gas chromatography/mass spectrometry

Rain and surface water samples from Southern Germany were investigated from 1991 to 1995 for terbuthylazine and one of its major metabolites, deethylterbuthylazine. The concentrations observed were compared to the concentrations found for atrazine and deethylatrazine in the same water samples. Concentrations ranged from < 0.02 μg/L to 0.7 μg/L for terbuthylazine and from < 0.02 μg/L to 0.6 μg/L fo
Authors
A. Dankwardt, E.M. Thurman, B. Hock

Occurrence of selected herbicides and herbicide degradation products in Iowa's Ground Water, 1995

Herbicide compounds were prevalent in ground water across Iowa, being detected in 70% of the 106 municipal wells sampled during the summer of 1995. Herbicide degradation products were three of the four most frequently detected compounds for this study. The degradation product alachlor ethanesulfonic acid was the most frequently detected compound (65.1%), followed by atrazine (40.6%), and the degra
Authors
D.W. Kolpin, S. J. Kalkhoff, D. A. Goolsby, D. A. Sneck-Fahrer, E.M. Thurman

Mixed-mode sorption of hydroxylated atrazine degradation products to sell: A mechanism for bound residue

This study tested the hypothesis that sorption of hydroxylated atrazine degradation products (HADPs: hydroxyatrazine, HA; deethylhydroxyatrazine, DEHA; and deisopropylhydroxyatrazine, DIHA) to soils occurs by mixed-mode binding resulting from two simultaneous mechanisms: (1) cation exchange and (2) hydrophobic interaction. The objective was to use liquid chromatography and soil extraction experime
Authors
R.N. Lerch, E.M. Thurman, E.L. Kruger

Assessing aquifer contamination risk using immunoassay: Trace analysis of atrazine in unsaturated zone sediments

The vulnerability of a shallow aquifer in south-central Kansas to contamination by atrazine (2-chloro-4-ethylamino-6-isopropylamines-triazine) was assessed by analyzing unsaturated zone soil and sediment samples from about 60 dryland and irrigated sites using an ultrasensitive immunoassay (detection level of 0.02 µg/kg) with verification by gas chromatography/mass spectrometry (GC/MS). Samples wer
Authors
K. E. Juracek, E.M. Thurman

Effect of tributary inflows on the distribution of trace metals in fine- grained bed sediments and benthic insects of the Clark Fork River, Montana

The effect of tributary inflows on metal concentrations in <63-μm sediments and benthic insects was examined on two scales (380 km and <2 km) in a river impacted by mining. A dilution−mixing model effectively described large-scale dispersion of Cd, Cu, and Pb in the sediments of the river. Input of metal from contaminated flood plains may introduce additional contamination in the middle reaches of
Authors
E.V. Axtmann, D.J. Cain, S. N. Luoma